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Sample records for na perekhod cs

  1. Evaluation of aqueous Na+/Cs+ separation by electrodialysis

    International Nuclear Information System (INIS)

    Buehler, M.F.; Lawrence, W.E.; Norton, J.D.

    1993-12-01

    In support of the Hanford Site cleanup, electrodialysis is being investigated as a method to separate aqueous sodium (Na + ) and cesium (Cs + ) ions. The approach has many advantages over existing separation technologies; in particular, electrodialysis creates little secondary waste while producing usable acid and base streams. The fundamentals of electrodialysis are presented in this report to provide a foundation for interpreting experimental data. A flat-plate laboratory-scale apparatus was used to determine the feasibility of separating Na + /Cs + mixtures by electrodialysis. The results showed that Cs + is preferentially separated over Na + by a factor of 2 to 3 using a Nafion reg-sign 417 cationic membrane. The separation is relatively insensitive to solution ionic strength and flow-rate variations. The current efficiency of the separation ranges from 0.60 to 0.65 depending on the applied voltage. The laboratory-scale system was characterized by dimensional analysis, which demonstrated that the process could be scaled up to a size attractive for the volume of waste at the Hanford Site. Preliminary experiments on a bench-scale system were also conducted. The initial results showed that the current-voltage response of the laboratory- and the bench-scale unit is identical

  2. Lattice dynamics of cubic Cs2NaLnX6 and CsNaLn1-xLn'xX6 elpasolites

    International Nuclear Information System (INIS)

    Acevedo, R.; Poblete, V.; Alzamora, R.; Venegas, R.; Navarro, G.; Henriquez, C.

    1999-01-01

    Crystal lattice dynamics of stoichiometric Cs 2 NaLnX 6 and nonstoichiometric CsNaLn 1-x Ln' x X 6 , 0.01 ≤ x ≤ 0.10, Ln and Ln' are trivalent positive lanthanide ions and X is chlorine or bromine, were studied.. Phonon dispersion relations were computed for similar compound, Cs 2 UBr 6 , and vibronic absorption spectra with reduced number of required input parameters are considered on the basis of proposed model. (author)

  3. Comparison of CsI(Tl) and CsI(Na) partially slotted crystals for high-resolution SPECT imaging

    International Nuclear Information System (INIS)

    Giokaris, N.; Loudos, G.; Maintas, D.; Karabarbounis, A.; Lembesi, M.; Spanoudaki, V.; Stiliaris, E.; Boukis, S.; Sakellios, N.; Karakatsanis, N.; Gektin, A.; Boyarintsev, A.; Pedash, V.; Gayshan, V.

    2006-01-01

    Dedicated systems based on Position Sensitive Photomultiplier Tubes (PSPMTs) coupled to scintillators, have been used over the past years for the construction of compact systems, suitable for applications such as small animal imaging and small organs imaging. Most of the proposed systems are based on fully pixelized scintillators. Previous studies have shown that partially slotted scintillators offer a good compromise between cost, energy resolution and spatial resolution. In this work, the performance of two sets of CsI(Tl) and CsI(Na) partially slotted crystals is compared. Initial results show that CsI(Tl) scintillators are more suitable for gamma-ray detection, since their performance in terms of sensitivity, spatial and energy resolution is superior than that of CsI(Na)

  4. Design and implementation of the NaI(Tl)/CsI(Na) detectors output signal generator

    International Nuclear Information System (INIS)

    Zhou Xu; Liu Congzhan; Zhao Jianling

    2014-01-01

    We designed and implemented a signal generator that can simulate the output of the NaI(Tl)/CsI(Na) detectors' pre-amplifier onboard the Hard X-ray Modulation Telescope (HXMT). Using the development of the FPGA (Field Programmable Gate Array) with VHDL language and adding a random constituent, we have finally produced the double exponential random pulse signal generator. The statistical distribution of the signal amplitude is programmable. The occurrence time intervals of the adjacent signals contain negative exponential distribution statistically. (authors)

  5. Design and implementation of the NaI(Tl)/CsI(Na) detectors output signal generator

    Science.gov (United States)

    Zhou, Xu; Liu, Cong-Zhan; Zhao, Jian-Ling; Zhang, Fei; Zhang, Yi-Fei; Li, Zheng-Wei; Zhang, Shuo; Li, Xu-Fang; Lu, Xue-Feng; Xu, Zhen-Ling; Lu, Fang-Jun

    2014-02-01

    We designed and implemented a signal generator that can simulate the output of the NaI(Tl)/CsI(Na) detectors' pre-amplifier onboard the Hard X-ray Modulation Telescope (HXMT). Using the development of the FPGA (Field Programmable Gate Array) with VHDL language and adding a random constituent, we have finally produced the double exponential random pulse signal generator. The statistical distribution of the signal amplitude is programmable. The occurrence time intervals of the adjacent signals contain negative exponential distribution statistically.

  6. Luminescent materials: Elpasolite Cs2NaGdCl6

    International Nuclear Information System (INIS)

    Poblete, V.; Martin, V; Acevedo, R.

    2000-01-01

    The non stoichiometric and stoichiometric elpasolites are highly attractive from the technological and spectroscopic point of view. Their applications in the laser industry, in the production of electroluminescent devices, in the preparation of superconductors, in the study of energy transfer processes and in the development of cyclic models for interpreting spectral intensity mechanisms, have awakened the interest of different investigators. Our working group is developing an ambitious multidisciplinary research project for which meticulous experimental and theoretical studies are being carried out with non stoichiometric and stoichiometric elpasolites. Different nuclear analytical techniques and other conventional techniques will be used to obtain enough updated experimental data to analyze the validity of our calculation models for the interpretation of what is physically observed. This paper presents the synthesis of the Cs 2 NaGdCCl 6 , elpasolite, whose crystallographic data has not yet been published in the literature. The synthesis process is carried out with a solid state reaction, in controlled atmosphere. Using thermal analysis (DTA/TGA), in a temperature range of 20 o C to 900 o C , the optimum conditions for thermal treatment are set at 775 o C for two hours. Structural studies are carried out using DRX, neutron diffraction and using computer programs (Rietveld's profile refining method), to obtain a network parameter. A comparison between both techniques of structural analysis is discussed, presenting the strengths and weaknesses of both methods and the outlook for their applications in the study of non stoichiometric elpasolites (C.W)

  7. Experimental studies of Cs, Sr, Ni, and Eu sorption on Na-illite and the modelling of Cs sorption

    International Nuclear Information System (INIS)

    Poinssot, C.; Baeyens, B.; Bradbury, M.H.

    1999-08-01

    A natural illite (illite du Puy) was purified and converted to the homo-ionic Na-form. The conditioned Na-illite was characterised in terms of its mineralogy, chemical inventory and physico-chemical properties. The structural formula was determined from energy dispersive spectroscopic analyses (SEM/TEM-EDS) and bulk chemistry measurements. A cation exchange capacity of 127 meq kg -1 was determined by the 22 Na isotope dilution method at neutral pH. The Na-CEC was also measured as a function of pH. The stability of Na-illite as a function of pH in the range between 3 and 6 was investigated. At low pH values partial dissolution of the illite occurs releasing the structural elements Al, Si, Mg, and K into solution. The presence of Ca and Sr in solution was interpreted as being due to desorption from cation exchange sites. All of these elements are also present at neutral pH but at considerably lower levels. Such effects cannot be avoided and must be considered in the interpretation of the sorption measurements. The main focus of the experimental work presented here is on the sorption behaviour of Cs, Sr, Ni and Eu on conditioned Na-illite as a function of NaClO 4 background electrolyte concentration (0.1 and 0.01 M), nuclide concentration and pH in the range between 3 and 11. Sorption edge data (R d versus pH) and sorption isotherms (quantity of nuclide sorbed versus equilibrium nuclide concentration) are presented for these four elements. Prior to beginning these experiments, sorption kinetics were measured. The broad based pool of sorption measurements generated from this work will provide the source data sets for subsequent modelling. So far only the Cs sorption measurements have been modelled. A two site cation exchange model was developed to describe the sorption of Cs over the whole range of experimental conditions. The two site types were termed 'frayed edge sites' (FES, high affinity/low capacity) and 'type II sites' (low affinity/high capacity). Selectivity

  8. Coprecipitation of 137Cs and 85Sr microquantities with complex compound [M(18-crown-6)]BPH4 (M=Na+, Cs+) from neutral and alkaline solutions

    International Nuclear Information System (INIS)

    Konovalova, N.A.; Rumer, I.A.; Kulyukhin, S.A.

    2009-01-01

    The paper reports the possibility of joint separation of 137 Cs and 85 Sr from neutral and alkaline aqueous solutions by their coprecipitation with the solid phase of complex compounds [M(18-crown-6)]BPh 4 (M=Na + , Cs + ), as well as to study the coprecipitation of 137 Cs and 85 Sr with the solid phase CsBPh 4 . It is found that complex compounds [M(18-crown-6)]BPh 4 (M=Na + , Cs + ) increased the degree of 85 Sr separation from solutions virtually two- to threefold vs. CsBPh 4 . Chloride and nitrate were found to have hardly any impact on the coprecipitation of 137 Cs and 85 Sr with [M(18-crown-6)]BPh 4 (M = Na + , Cs + ). (orig.)

  9. Effect of He pressure on the superconducting transition temperatures of Na2CsC60 and (NH3)4Na2CsC60

    International Nuclear Information System (INIS)

    Schirber, J.E.; Bayless, W.R.; Rosseinsky, M.J.; Zhou, O.; Fleming, R.M.; Murphy, D.; Fischer, J.E.

    1994-01-01

    The Na based mixed alkali doped C 60 superconductors show anomalous behavior with respect to the ''universal'' superconducting transition temperature T c vs lattice constant a 0 relation followed by most of the fcc A 3 C 60 superconductors. We have measured dt c /dP for Na 2 CsC 60 and (NH 3 ) 4 Na 2 CsC 60 using solid He as the pressure medium to ∼ 6 kbar finding dT c /dP equal to -0.8±(0.01) K/kbar and -1.0(±0.1)K/kbar for Na 2 CsC 60 and Na 2 (NH 3 ) 4 C 60 respectively. Our value for Na 2 CsC 60 differs markedly from that obtained by Mizuki et al of about -1.3 K/kbar. However, using N 2 or Ar, we obtain values for dT c /dP in substantial agreement with Mizuki et al who used fluorinert to generate their pressure. This work emphasizes the need for compressibility measurements with the same pressure medium in the appropriate temperature range so that meaningful comparisons can be made between various pressure measurements and models which are based on lattic spacing

  10. Phase-separated CsI-NaCl scintillator grown by the Czochralski method

    Science.gov (United States)

    Yasui, Nobuhiro; Kobayashi, Tamaki; Ohashi, Yoshihiro; Den, Toru

    2014-08-01

    A phase-separated CsI-NaCl scintillator with light-guiding properties was grown by the Czochralski method. The CsI-NaCl eutectic phase usually consists of NaCl cylinders in a CsI matrix and contains grain boundaries. However, we have grown composites without grain boundaries by creating a convex solid/liquid interface, selecting a single grain by Dash's neck method, and increasing the diameter of the composite moderately. The good continuous convection flow required for these conditions was achieved by suppressing the drop in the aspect ratio of the melt height to the crucible radius with a double crucible setup. We successfully obtained a CsI-NaCl:Tl composite that was uniform with no grain boundaries greater than 30 mm in diameter.

  11. Synthesis and structural characterization of luminescent inorganic materials of the type CS2NaErBr6 and CS2NaHoBr6

    International Nuclear Information System (INIS)

    Poblete, V.H.; Fack, G.

    2001-01-01

    The synthesis and structural characterization is described of two luminescent materials, with technological [1] and spectroscopic [2] interest, whose crystallographic charts have not been published in the literature. The synthesis of both systems: Cs 2 NaErBr 6 and CS 2 NaHoBr 6 , was done using solid state reactions in a controlled environment. The thermal analyses DTA/TGA, applied with a temperature gradient of 10 o C/min., established crystallization ranges of 490,4 o C to 545,4 o C, for the elpasolite CS 2 NaHoBr 6 and 501 o C to 556 o C, for the structure CS 2 NaErBr 6 .. The heat vacuum treatments were carried out at 505 o C and 526 o C respectively, obtaining optimum crystallization. The structural characterization was performed with powdered X-ray diffraction (XRD). The range between 12 o and 80 o (2θ), was analyzed for 3352 points, measured steps of 0.02 o (2θ using the Rietveld profile refining program. The following crystallographic parameters were established: a 0 = 11,279(1), and 11,293(4) Angstroms, for the two structures analyzed, respectively. The relationship R exp wp in both cases is highly accurate for the 32 test lines that were analyzed. The structures present cubic closed packing Cs 1+ 3 Cl 1- , with Ho 3+ and Er 3+ atoms, filling the octahedral holes. The test data obtained will be very useful for completing the mass of experimental data needed to develop the design engineering, with specific applications for luminescent devices

  12. Synthesis and structural characterization of inorganic luminescent materials of Cs2NaErBr6 and Cs2NaHoBr6

    International Nuclear Information System (INIS)

    Poblete, V.H; Fack, G

    2003-01-01

    The synthesis and structural characterization is described of two luminescent materials, with technological [1] and spectroscopic [2] interest, whose crystallographic charts have not been published in the literature. The synthesis of both systems: Cs 2 NaErBr 6 and CS 2 NaHoBr 6 , was done using solid state reactions in a controlled environment. The thermal analyses DTA/TGA, applied with a temperature gradient of 10 o C/min., established crystallization ranges of 490,4 o C to 545,4 o C, for the elpasolite CS 2 NaHoBr 6 and 501 o C to 556 o C, for the structure CS 2 NaErBr 6 .. The heat vacuum treatments were carried out at 505 o C and 526 o C respectively, obtaining optimum crystallization. The structural characterization was performed with powdered X-ray diffraction (XRD). The range between 12 o and 80 o (2θ), was analyzed for 3352 points, measured steps of 0.02 o (2θ using the Rietveld profile refining program. The following crystallographic parameters were established: a 0 = 11,279(1), and 11,293(4) Angstroms, for the two structures analyzed, respectively. The relationship R exp wp in both cases is highly accurate for the 32 test lines that were analyzed. The structures present cubic closed packing Cs 1+ 3 Cl 1- , with Ho 3+ and Er 3+ atoms, filling the octahedral holes. The test data obtained will be very useful for completing the mass of experimental data needed to develop the design engineering, with specific applications for luminescent devices (au)

  13. Mutual influence of the Na+ and Cs+ ions during their mass electrotransport through a perfluorinated sulfocation membrane

    International Nuclear Information System (INIS)

    Zezina, E.A.; Popkov, Yu.M.; Timashev, S.F.

    1997-01-01

    It is shown that by the Na + and Cs + ions sorption equilibrium conditions in perfluorinated cation-exchange membranes from the 0.1M NaCl and 0.1M CsCl mixtures the Cs + ions are sorbed primarily. The effective self-diffusion coefficients of the Na + and Cs + ions from individual solutions within the range of 0.01-1.00 M concentrations and in the above-mentioned equimolar mixture are found. It is shown that the membranes moisture content is the determining factor for the Cs + ions electrodialysis separation fro the above-mentioned electrolytes mixture

  14. Absorption spectra and Faraday effect in Cs2NaNdCl6 and Cs2NaPrCl6 crystals

    International Nuclear Information System (INIS)

    Ehdel'man, I.S.; Galanov, E.K.; Kokov, I.T.; Malakhovskij, A.V.; Anistratov, A.T.

    1985-01-01

    The paper is devoted to studying absorption spectra and the Faraday effect in Cs 2 NaNdCl 6 and Cs 2 NaPrCl 6 crystals. The absorption spectra and Faraday effect were measured at room temperature in the range of 9000-30000 cmsup(-1) (0.33-1.2 μm) in 0-10 kOe magnetic fields. The absorption spectra produced contain several groups of intense absorption bands resulted from intraconfiguration electron transitions in rare-earth cations. The Faraday spectra in the whole range studied for both crystals have the form of smoothly dipping curves when increasing wavelength. The form of these curves testifies to prevailing contribution of strong electron transitions lying in a nearer UV region to the Faraday effect

  15. Role of activators and vacancies in the gamma-scintillation decay in CsI-Na

    International Nuclear Information System (INIS)

    Panova, A.N.; Grinev, B.V.; Sojfer, L.M.; Shakhova, K.V.; Kosinov, N.N.; Mitichkin, A.I.; Korsunova, S.P.; Lavrent'ev, F.F.

    2004-01-01

    We studied the influence of activator concentration (CNaI) and plastic deformation on the change in the contribution of the slow component to the decay of gamma-scintillation in CsI-Na crystals. The influence of CNaI on the change in the form of the luminescence excitation spectrum in the region of the absorption of activator centers (AC) and centers of vacancy nature (VNC) is investigated. The effect of CNaI on the change in the intercenter decay time of the mentioned centers is studied too. It is shown that AC and VNC participate in the photoluminescence and gamma-scintillations of CsI-Na crystals. In gamma-scintillations AC are responsible for the component τ i 370 ns, whereas the components τ 1 ' = 460 ns and τ 2 ∼ 2 μs are bound up with VNC. The decrease of τ γ from 770 to 560 ns with the growth of C from 2·10 -3 to 3·10 -2 mol. % NaI, and after plastic deformation of the crystals (ε = 5 %) along the axis from 570 to 470 ns is caused by the decrease in the number of VNC. Mechanisms of gamma-scintillations of CsI-Na crystals AC and VNC, as well as the decrease in the number of VNC are discussed. (authors)

  16. Temporal evolution of 137Cs+, K+ and Na+ in fruits of South American tropical species

    International Nuclear Information System (INIS)

    Cid, A.S.; Anjos, R.M.; Zamboni, C.B.; Velasco, H.; Macario, K.; Rizzotto, M.

    2013-01-01

    Concentrations of 137 Cs, K and Na in fruits of lemon (Citrus limon B.) and of K and Na in fruits of coconut (Cocos nucifera L.) trees were measured by both gamma spectrometry and neutron activation analysis, with the aim to understand the behaviour of monovalent inorganic cations in tropical plants as well as the plant ability to store these elements. Similar amounts of K + were incorporated by lemon and coconut trees during the growth and ripening processes of its fruits. The K concentration decreased exponentially during the growth of lemons and coconuts, ranging from 13 to 25 g kg −1 dry weight. The incorporation of Na + differed considerably between the plant species studied. The Na concentration increased linearly during the lemon growth period (0.04 to 0.70 g kg −1 d.w.) and decreased exponentially during the coconut growth period (1.4 to 0.5 g kg −1 d.w.). Even though radiocaesium is not an essential element to plants, our results have shown that 137 Cs incorporation to vegetable tissues is positively correlated to K distribution within the studied tropical plant species, suggesting that the two elements might be assimilated in a similar way, going through the biological cycle together. A mathematical model was developed from the experimental data allowing simulating the incorporation process of monovalent inorganic cations by the fruits of such tropical species. The agreement between the theoretical approach and the experimental values is satisfactory along fruit development. - Highlights: ► Concentrations of 137 Cs, K and Na in fruits of lemon (Citrus limon B.) are presented. ► Concentrations of K and Na in fruits of coconut (Cocos nucifera L.) are also showed. ► We investigated the use of 137 Cs as a tracer for the plant absorption of macronutrients. ► A model was developed to simulate the temporal evolution of 137 Cs, K and Na by fruits. ► This model exhibited close agreement with our results along the fruit development

  17. Effect of alkali ions (Na+, K+, Cs+) on reaction mechanism of CZTS nano-particles synthesis

    Science.gov (United States)

    Kumar, Suresh; Altosaar, Mare; Grossberg, Maarja; Mikli, Valdek

    2018-04-01

    The control of morphology, elemental composition and phase composition of Cu2ZnSnS4 (CZTS) nano-crystals depends on the control of complex formation and surface stabilization of nano-particles in solution-based synthesis in oleylamine. At temperatures ≥280 °C, the control of nano-crystal's morphology and homogenous growth is difficult because of fast poly-nuclear growth occurring at higher temperatures. In the present work the effect of oleylamine complex formation with different alkali ions (Na+, K+ and Cs+) on nano-crystals growth at synthesis temperature of 280 °C was studied. It was found that nano-powders synthesized in the presence of Na+ and K+ ions showed the formation of crystals of different sizes - small nano-particles (18 nm-30 nm), large aggregated crystals (few nm to 1 μm) and large single crystals (1 μm - 4 μm). The presence of Cs+ ions in the nano-powder synthesis in oleylamine-metal precursor-CsOH solution promoted growth of nano-crystals of homogenous size. It is proposed that the formed oleylamine-Cs complexes a) enhance the formation and stabilization of oleylamine-metal (Cu, Zn and Sn) complexes before the injection of sulphur precursor into the oleylamine-metal precursor solution and b) after addition of sulphur stabilize the fast nucleated nano-particles and promote diffusion limited growth.

  18. Selective removal of Cs and Re by precipitation in a Na2CO3-H2O2 solution

    International Nuclear Information System (INIS)

    Eil-Hee Lee; Jae-Gwan Lim; Dong-Yong Chung; Han-Beom Yang; Kwang-Wook Kim

    2010-01-01

    The removal of Cs and Re (as a surrogate for Tc) by selective precipitation from the simulated fission products which were co-dissolved with uranium during the oxidative dissolution of spent fuel in a Na 2 CO 3 -H 2 O 2 solution was investigated in this study. The precipitations of Cs and Re were examined by introducing sodium tetraphenylborate (NaTPB) and tetraphenylohosponium chloride (TPPCl), respectively. The precipitation of Cs by NaTPB and that of Re by TPPCl each took place within 5 min, and an increase in temperature up to 50 deg C and a stirring speed up to 1000 rpm hardly affected their precipitation rates. The most important factor in the precipitation with NaTPB and TPPCl was found to be a pH of the solution after precipitation. Since Mo tends to co-precipitate with Cs or Re at a lower pH, an effective precipitation with NaTPB and TPPCl was done at pH of above 9 without the co-precipitation of Mo. More than 99% of Cs and Re were precipitated when the initial concentration ratio of NaTPB to Cs was above 1 and when that of TPPCl to Re was above 1. The precipitation of Cs and Re was never affected by the concentration of Na 2 CO 3 and H 2 O 2 , even though they were raised up to 1.5 and 1.0 M, respectively. Precipitation yields of Cs and Re in a Na 2 CO 3 -H 2 O 2 solution were found to be dependent on the concentration ratios of [NaTBP]/[Cs] and [TPPCl]/[Re]. (author)

  19. Electronic Spectra of Cs2NaYb(NO2)6: Is There Quantum Cutting?

    Science.gov (United States)

    Luo, Yuxia; Liu, Zhenyu; Hau, Sam Chun-Kit; Yeung, Yau Yuen; Wong, Ka-Leung; Shiu, Kwok Keung; Chen, Xueyuan; Zhu, Haomiao; Bao, Guochen; Tanner, Peter A

    2018-05-03

    The crystal structure and electronic spectra of the T h symmetry hexanitritoytterbate(III) anion have been studied in Cs 2 NaY 0.96 Yb 0.04 (NO 2 ) 6 , which crystallizes in the cubic space group Fm3̅. The emission from Yb 3+ can be excited via the NO 2 - antenna. The latter electronic transition is situated at more than twice the energy of the former, but at room temperature, one photon absorbed at 470 nm in the triplet state produces no more than one photon emitted. Some degree of quantum cutting is observed at 298 K under 420 nm excitation into the singlet state and at 25 K using excitation into either state. The quantum efficiency is ∼10% at 25 K. The energy level scheme of Yb 3+ has been deduced from excitation and emission spectra and calculated by crystal field theory. New improved energy level calculations are also reported for the Cs 2 NaLn(NO 2 ) 6 (Ln = Pr, Eu, Tb) series using the f- Spectra package. The neat crystal Cs 2 NaYb(NO 2 ) 6 has also been studied, but results were unsatisfactory due to sample decomposition, and this chemical instability makes it unsuitable for applications.

  20. Alpha-gamma pulse shape discrimination in CsI:Tl, CsI:Na and BaF sub 2 scintillators

    CERN Document Server

    Dinca, L E; Haas, J; Bom, V R; Eijk, C W E

    2002-01-01

    Some scintillating materials offer the possibility of measuring well separated alpha and gamma scintillation response using a single crystal. Eventually aiming at thermal neutron detection using sup 6 Li or sup 1 sup 0 B admixture, pulse shape discrimination measurements were made on three scintillators: CsI:Tl, CsI:Na and pure BaF sub 2 crystals. A very good alpha/gamma discrimination was obtained using sup 2 sup 2 Na, sup 2 sup 4 sup 1 Am (gamma) and sup 2 sup 4 sup 4 Cm (alpha) radioactive sources.

  1. Development of low background CsI(Tl) and NaI(Tl) crystals for WIMP search

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Hyun Su [Department of Physics, Ewha Womans University, Seoul 120-750 (Korea, Republic of)

    2015-08-17

    We have developed low background CsI(Tl) and NaI(Tl) crystals to search for weakly interacting massive particles as well as to verify the origin of the annual modulation signal observed by the DAMA/LIBRA experiment. Extensive studies about the contamination mechanisim of {sup 137}Cs in CsI powder lead to the growth of ultra-low-background CsI(Tl) crystals. Similar approaches for NaI(Tl) crystals have been applied to reduce internal backgrounds to less than 0.5 counts/kg/day/keV. Status and understanding of backgrounds and background reduction in NaI(Tl) crystals will be discussed.

  2. Effect of crystal shape, size and reflector type on operation characteristics of gamma-radiation detectors based on CsI(Tl) and CsI(Na) scintillators

    International Nuclear Information System (INIS)

    Globus, M.E.; Grinyov, B.V.; Ratner, M.A.

    1996-01-01

    Operation characteristics of CsI(Tl) and CsI(Na) scintillation detectors, to a large degree connected with light collection in crystals, are calculated for various shapes, sizes and reflecting surface types. Allowance is made for the true light reflection indicatrix which is characterized by the effective mirror constituent of the reflected light, p. Its value , averaged over incidence angle, is used for the classification of reflecting surfaces. Operation characteristics (in particular, spectrometric ones) are found to be essentially dependent on . Tables of operation characteristics, given below, permit one to make inferential conclusions on an optimal combination of the shape, sizes an the reflecting surface version

  3. Accumulation of Cs, Sr into leaves and grain of winter wheat under act of N, Zn, Li, Na

    International Nuclear Information System (INIS)

    Grodzinsky, D.; Tkatchuk, K.; Zhmurko, N.; Bogdan, T.; Guralchuk, Zh.

    1998-01-01

    The experiments were carried out on cv Lutencens 7 winter wheat grown on grey forest soil. In order to study the influence of nitrogen on Cs and Sr accumulation, a background of P60 K60 added in autumn different doses of nitrogen (30, 60, 120 kg/ha) were applied in spring. The influence of micronutrients on Cs and Sr accumulation was studied by adding 3 kg/ha Zn and 2 kg/ha Li to the soil under ploughing on background of N60 P60 K60. Besides the foliar application with 0.05% Na 2 SO 4 was carried out. Cation content (Cs, Sn, Zn, Li, Na) in soil and plant organs was determined by atomic absorption spectrophotometry. The Cs, Sr content in control plant leaves made up 15.0 and 21.0 mg per g of dry matter at the early stages of plant development. As the plants aged, the content of those elements in the leaves decreased strongly (3-4 times). At early stages of plant development, nitrogen caused an 8.9-11% increase in the Cs content of the leaves. At the stages of heading to grain filling, the Cs content increase was only observed at a high nitrogen dose, whereas low nitrogen doses had no effected on Cs accumulation in leaves. In should be noted that nitrogen (N60 and N120) decreased the Cs content in grain by 32-33%. As for the Sr content of grain, this was 3 to 4-fold less than that of Cs. Nitrogen had no effected on the Sr content of grain. Zn and Li addition to soil as well as foliar nutrition with Na had a different effect on the Cs and Sr content of winter wheat leaves and grain. Addition of Li decreased the Cs and Sr content of old leaves by 13% and 25% respectively. Addition of Zn and Na decreased the Sr content of old leaves but had no effect on the Cs content. Zn, Na and Li reduced the Sr content in grain also, viz. by 16,11 and 7% respectively. Thus the research has demonstrated the possibility of regulating Cs and Sr accumulation in the above-ground organs of winter wheat plants

  4. Thermodynamic properties of thulium and ytterbium in fused NaCl-KCl-CsCl eutectic

    Energy Technology Data Exchange (ETDEWEB)

    Novoselova, A., E-mail: A.Novoselova@ihte.uran.ru [Institute of High-Temperature Electrochemistry, Ural Division, Russian Academy of Science, S. Kovalevskaya Str., 22, Ekaterinburg 620990 (Russian Federation); Smolenski, V. [Institute of High-Temperature Electrochemistry, Ural Division, Russian Academy of Science, S. Kovalevskaya Str., 22, Ekaterinburg 620990 (Russian Federation)

    2011-07-15

    Research highlights: > Tm and Yb chloride compounds as fission products. > The investigation of electrochemical properties of lanthanides. > Determination of the apparent standard redox potentials of the couple Ln(III)/Ln(II) in fused NaCl-KCl-CsCl eutectic at (823 to 973) K. > The calculation of the basic thermodynamic properties of redox reaction in molten salt. - Abstract: This work presents the results of a study of the Tm{sup 3+}/Tm{sup 2+} and Yb{sup 3+}/Yb{sup 2+} couple redox potentials vs. Cl{sup -}/Cl{sub 2} reference electrode at the temperature range (823 to 973) K in fused NaCl-KCl-CsCl eutectic by direct potentiometric method. Initial concentrations of TmCl{sub 3} and YbCl{sub 3} in solvents did not exceed 5.0 mol%. Basic thermodynamic properties of the reactions TmCl{sub 2(l)} + 1/2 Cl{sub 2(g)} {r_reversible} TmCl{sub 3(l)} and YbCl{sub 2(l)} + 1/2 Cl{sub 2(g)} {r_reversible} YbCl{sub 3(l)} were calculated using the temperature dependencies of apparent standard potentials of the couples E{sub Tm{sup 3+}/Tm{sup 2+*}} and E{sub Yb{sup 3+}/Yb{sup 2+*}}.

  5. Expression of colonization factor CS5 of enterotoxigenic Escherichia coli (ETEC is enhanced in vivo and by the bile component Na glycocholate hydrate.

    Directory of Open Access Journals (Sweden)

    Matilda Nicklasson

    Full Text Available Enterotoxigenic Escherichia coli (ETEC is an important cause of acute watery diarrhoea in developing countries. Colonization factors (CFs on the bacterial surface mediate adhesion to the small intestinal epithelium. Two of the most common CFs worldwide are coli surface antigens 5 and 6 (CS5, CS6. In this study we investigated the expression of CS5 and CS6 in vivo, and the effects of bile and sodium bicarbonate, present in the human gut, on the expression of CS5. Five CS5+CS6 ETEC isolates from adult Bangladeshi patients with acute diarrhoea were studied. The level of transcription from the CS5 operon was approximately 100-fold higher than from the CS6 operon in ETEC bacteria recovered directly from diarrhoeal stool without sub-culturing (in vivo. The glyco-conjugated primary bile salt sodium glycocholate hydrate (NaGCH induced phenotypic expression of CS5 in a dose-dependent manner and caused a 100-fold up-regulation of CS5 mRNA levels; this is the first description of NaGCH as an enteropathogenic virulence inducer. The relative transcription levels from the CS5 and CS6 operons in the presence of bile or NaGCH in vitro were similar to those in vivo. Another bile salt, sodium deoxycholate (NaDC, previously reported to induce enteropathogenic virulence, also induced expression of CS5, whereas sodium bicarbonate did not.

  6. Processing of radioactive waste solution with zeolites. I. Thermal transformation of Na, Cs and Sr type zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Kanno, T; Mimura, H; Kitamura, T [Tohoku Univ., Sendai (Japan). Research Inst. of Mineral Dressing and Metallurgy

    1976-08-01

    Thermal transformation of Na, Cs and Sr type zeolites were studied by means of differential thermal analysis (DTA), thermogravimetric analysis (TGA) and X-ray powder diffraction. Synthetic zeolites A, X and Y, synthetic mordenite (Zeolon) and natural mordenite were used in this study. Na type zeolites of A and X recrystallized to Nepheline (NaAlSiO/sub 4/) above 1,000/sup 0/C, but the structures of zeolite Y and mordenite collapsed above about 900/sup 0/C and did not recrystallize until 1,200/sup 0/C. Cs type zeolites of A and X recrystallized to pollucite (CsAlSi/sub 2/O/sub 6/) above 1,000/sup 0/C and Cs type of zeolite Y recrystallized to it above 1,100/sup 0/C, but the structure of mordenite collapsed above 1,000/sup 0/C and did not recrystallize until 1,200/sup 0/C. On Sr type zeolites, zeolite A and X recrystallized to strontium aluminosilicate (SrAl/sub 2/Si/sub 2/O/sub 8/) above 1,100/sup 0/C and zeolite Y recrystallized to it above 1,200/sup 0/C, but the structure of mordenite collapsed above 1,000/sup 0/C. The results described above were supported by microscopic observation and the measurement of density. If this solidifications by calcination of zeolites are further studied, new informations concerning the fixation of Cs and Sr will be obtained.

  7. Pulse shaper for scintillation detectors with NaI(Tl) or CsI(Tl) crystals

    International Nuclear Information System (INIS)

    Novisov, B.S.; Maksimenko, A.S.; Baryshev, A.V.; Zhukov, A.V.

    1978-01-01

    The basic circuit of a signal shaper for scintillation detectors with NaI(Tl) and CsI(Tl) crystals is described. To increase amplitude resolution, it is suggested to integrate not the whole charge at the photomultiplier output, but a part of the charge during the initial 100 ns of the current pulse; the remaining part of the current signal is compensated directly at the photomultiplier anode by means of an electric circuit. The principal elements of the spectrometric signal shaper include an input transistor amplifier, a compensation circuit, a key element, a shaper amplifier of time pulses, a shaper of signal duration for controlling the key element, and an output spectrometric amplifier. This device, being used, one can shape pulses at durations of 100 ns and more. The shaper restoration time does not exceed 50 ns. When the shaper operates with NaI(Tl) crystals and at counting rate of 10 6 pulse/s, the amplitude resolution with and without the compensation circuit is 17% and 21% respectively

  8. Validation of CsNaIF data evaluation software. Final report on task FIN A940 on the Finnish support programme to IAEA safeguards

    International Nuclear Information System (INIS)

    Kaartinen, J.

    1996-07-01

    A new computer programme, called CsNaIF, which calculates the area of 137 Cs peak in spent fuel spectra has been developed for IAEA. This programme has been tested and evaluated in this report. Evaluation has been made by calculating different types of SFAT spectra (NaI- and CdTe-SFAT) with the validated software and with a research grade gamma spectroscopy software, SAMPO 90. Obtained results, mainly 137 Cs peak areas and their errors, have been compared and perceived differences have been reported. Also some recommendations of the usability of CsNaIF programme have been made for IAEA. (orig.) (4 refs.)

  9. Na, Rb and Cs partitioning between metal, silicate and sulfide: Implications for volatile depletion in terrestrial planets

    Science.gov (United States)

    Boujibar, A.; Fei, Y.; Du, Z.; Righter, K.; Bullock, E. S.

    2017-12-01

    Inner Solar System materials are known for their depletion in volatile elements, including the moderately volatile alkalis: Na, K, Rb, and Cs. The origin of this depletion is still uncertain, as several processes could have been involved, during the nebular condensation or planetary accretion. Volatile depletion is commonly estimated through comparison of alkali concentrations relatively to those of chondrites, assuming they remain in planetary mantles during core segregation. However, experimental studies show that substantial K can partition into metals that are enriched in sulfur and oxygen. Several models have also suggested that sulfides may have played an important role during episodes of sulfide segregation from a crystallizing magma ocean (sulfide matte) or accretion of S-rich planetary embryos. For Mercury, a sulfide layer could be present between core and mantle, due to immiscibility between Si-rich and S-rich metals. Therefore, here we investigate whether alkali elements (Na, Cs and Rb) could be partly sequestered in planetary cores during their differentiation. We conducted experiments at high pressure and temperature (1 to 5 GPa and up to 1900 °C) to determine partition coefficients of Na, Rb and Cs between metal and silicate. Our results show that pressure, temperature, sulfur and oxygen in metals enhance the partitioning of Na, Rb and Cs into metals, as previously found for K. For all three investigated alkalis (Na, Rb and Cs), we found a maximum partition coefficient of 1 between sulfides containing 13 wt% O and silicate melt. Therefore, S-rich cores or sulfide layers formed due to immiscibility in Fe-S-O systems could have acted as important geochemical reservoirs for alkali elements. Using our experimental data and different assumptions on initial bulk abundances, we evaluate volatile depletion in terrestrial planets, by comparing resulting mantle alkali concentrations after core segregation, with actual concentrations in the Earth's mantle.

  10. New selective ligands for caesium. Application to Cs+/Na+ separation by nano-filtration-complexation in aqueous phase

    International Nuclear Information System (INIS)

    Pellet-Rostaing, S.; Chitry, F.; Lemaire, M.; Guy, A.; Foos, J.

    2000-01-01

    Separating traces of caesium from aqueous medium containing high sodium concentration is a harsh problem because caesium and sodium have a similar behaviour in aqueous medium. The aim of our study was to select a highly caesium-selective ligand in a nano-filtration-complexation process in order to achieve Cs + /Na + separation. This process involve a nano-filtration step combined with a preliminary complexation step. Caesium complexes are retained by the nano-filtration membrane whereas free sodium cations pass through it. We tried to find a relation between the ligands structure and their activity towards caesium-complexation. Among the synthesized receptors, Tetra-hydroxylated bis-crown-6 calix[4]arene was found to be the more caesium-selective ligand (S=β(Cs + )/β(Na+)=6600). Combined with a nano-filtration process, this ligand helped reaching 90% caesium retention in a highly concentrated aqueous medium ([NaNO 3 ] = 3 mol/L). (authors)

  11. Spectral intensities in cubic systems. III. The Cs2NaEuCl6 system

    International Nuclear Information System (INIS)

    Acevedo, R.; Hurtado, O.; Meruane, T.; Navarro, G.; Diaz, V.; Pozo, J.

    1998-01-01

    The optical properties of Cs 2 NaEuCl 6 system are reinvestigated on the basis of new and updated experimental data from Raman, electronic Raman, Infrared absorption and visible luminescence. These experimental studies have enable scientist to identify and assign all of the energy levels and corresponding electronic transitions up to 21500 cm -1 . Furthermore, the crystal field level identification from absorption spectroscopy has been confirmed from the additional emission and electronic Raman studies. We decided to study the most likely intensify mechanisms for this system, based upon these new experimental data and a modified version of a combined vibronic formalism, which takes into account the closure procedure for the intermediate electronic states. The total and relative vibronic intensity distributions are calculated and compared with the experimental data, when available. It is shown that the present calculation model although complex uses a minimum set of adjustable parameters from experimental data. The advantages and disadvantages of our physical models and calculation methods are compared with those of other authors and a full discussion is put forward in this paper. (Author)

  12. Vibronic intensities for Er3+ in Cs2 NaErCl6

    International Nuclear Information System (INIS)

    Acevedo, R.; Navarro, G.; Meruane, T.

    2001-01-01

    In this current study, we have undertaken vibronic intensity calculations for the absorptions (( 4 I 15/2 ) Γ k ) → (( 4 I 13/2 ) Γ l ) of the Er 3+ in the Cs 2 NaErCl 6 elpasolite type system. This system is extremely complicated to handle from both a theoretical and an experimental viewpoints. This theoretical work shows that over an energy range of about 400 cm -1 , a substantial amount of transitions are likely to take place (about 100 transitions; twenty five of them are magnetic dipole allowed and seventy five are vibronically allowed). It is then a formidable task to identify and assign all of these transitions in a non-ambiguous way. Also the experimental evidence available for these absorptions is related to a total of about twenty lines in the luminescence spectrum of this system. The spectrum itself is very challenging and the superposition of spectral features is most likely to occur. A careful analysis of the calculated vibronic intensities and overall oscillator strengths for the various transitions indicates that the current model used is both flexible and appropriate to deal with this kind of systems. In a forthcoming paper, we will examine the rather unusual high intensity associated with the (( 4 I 15/2 ) Γ k ) → (( 4 S 3/2 ) Γ l ) excitations. (Author)

  13. Phonon spectra of elpasolites Cs{sub 2}NaRF{sub 6} (R=Y,Yb): Ab initio calculations

    Energy Technology Data Exchange (ETDEWEB)

    Chernyshev, Vladimir, E-mail: Vladimir.Chernyshev@urfu.ru; Petrov, Vladislav; Nikiforov, Anatoliy; Zakiryanov, Dmitriy [Ural Federal University, Ekaterinburg (Russian Federation)

    2015-12-07

    The influence of hydrostatic pressure on structure and dynamics of a crystal lattice of elpasolites Cs{sub 2}NaYbF{sub 6} and Cs{sub 2}NaYF{sub 6} (S.G. 225) within ab initio approach is investigated. Frequencies and irreducible representations (irreps) of phonon modes are determined. Elastic constants are calculated. The calculations are carried out within MO LCAO approach using DFT method with hybrid functionalities of B3LYP and PBE0 in CRYSTAL09 periodic code. For the description of rare earth ion the pseudopotential replacing internal orbitals including 4f orbitals was used. External 5s and 5p orbitals defining chemical bond were described by valence basis sets.

  14. Synthesis, structural and spectroscopic properties of acentric triple molybdate Cs{sub 2}NaBi(MoO{sub 4}){sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Savina, A.A. [Laboratory of Oxide Systems, Baikal Institute of Nature Management, SB RAS, Ulan-Ude 670047 (Russian Federation); Department of Chemistry, Buryat State University, Ulan-Ude 670000 (Russian Federation); Atuchin, V.V., E-mail: atuchin@isp.nsc.ru [Laboratory of Optical Materials and Structures, Rzhanov Institute of Semiconductor Physics, SB RAS, Novosibirsk 630090 (Russian Federation); Functional Electronics Laboratory, Tomsk State University, Tomsk 634050 (Russian Federation); Laboratory of Semiconductor and Dielectric Materials, Novosibirsk State University, Novosibirsk 630090 (Russian Federation); Solodovnikov, S.F. [Laboratory of Crystal Chemistry, Nikolaev Institute of Inorganic Chemistry, SB RAS, Novosibirsk 630090 (Russian Federation); Department of Natural Sciences, Novosibirsk State University, Novosibirsk 630090 (Russian Federation); Solodovnikova, Z.A. [Laboratory of Crystal Chemistry, Nikolaev Institute of Inorganic Chemistry, SB RAS, Novosibirsk 630090 (Russian Federation); Krylov, A.S. [Laboratory of Molecular Spectroscopy, Kirensky Institute of Physics, SB RAS, Krasnoyarsk 660036 (Russian Federation); Maximovskiy, E.A. [Laboratory of Epitaxial Layers, Nikolaev Institute of Inorganic Chemistry, SB RAS, Novosibirsk 630090 (Russian Federation); Laboratory of Research Methods of Composition and Structure of Functional Materials, Novosibirsk State University, Novosibirsk 630090 (Russian Federation); Molokeev, M.S. [Laboratory of Crystal Structure, Kirensky Institute of Physics, SB RAS, Krasnoyarsk 660036 (Russian Federation); Oreshonkov, A.S [Laboratory of Molecular Spectroscopy, Kirensky Institute of Physics, SB RAS, Krasnoyarsk 660036 (Russian Federation); Department of Photonics and Laser Technology, Siberian Federal University, Krasnoyarsk 660079 (Russian Federation); Pugachev, A.M. [Laboratory of Condenced Matter Spectroscopy, Institute of Automation and Electrometry, SB RAS, Novosibirsk 90, 630090 (Russian Federation); and others

    2015-05-15

    New ternary molybdate Cs{sub 2}NaBi(MoO{sub 4}){sub 3} is synthesized in the system Na{sub 2}MoO{sub 4}–Cs{sub 2}MoO{sub 4}–Bi{sub 2}(MoO{sub 4}){sub 3}. The structure of Cs{sub 2}NaBi(MoO{sub 4}){sub 3} of a new type is determined in noncentrosymmetric space group R3c, a=10.6435(2), c=40.9524(7) Å, V=4017.71(13) Å{sup 3}, Z=12 in anisotropic approximation for all atoms taking into account racemic twinning. The structure is completely ordered, Mo atoms are tetrahedrally coordinated, Bi(1) and Bi(2) atoms are in octahedra, and Na(1) and Na(2) atoms have a distorted trigonal prismatic coordination. The Cs(1) and Cs(2) atoms are in the framework cavities with coordination numbers 12 and 10, respectively. No phase transitions were found in Cs{sub 2}NaBi(MoO{sub 4}){sub 3} up to the melting point at 826 K. The compound shows an SHG signal, I{sub 2w}/I{sub 2w}(SiO{sub 2})=5 estimated by the powder method. The vibrational properties are evaluated by Raman spectroscopy, and 26 narrow lines are measured. - Graphical abstract: - Highlights: • The crystal structure of Cs{sub 2}NaBi(MoO{sub 4}){sub 3} is defined. • The molybdate Cs{sub 2}NaBi(MoO{sub 4}){sub 3} is stable up to melting point at 826 K. • Vibrational properties of Cs{sub 2}NaBi(MoO{sub 4}){sub 3} are evaluated by Raman spectroscopy.

  15. Diffusion of Na(I), Cs(I), Sr(II) and Eu(III) in smectite rich natural clay.

    Science.gov (United States)

    Kasar, Sharayu; Kumar, Sumit; Bajpai, R K; Tomar, B S

    2016-01-01

    Diffusion of Na(I), Cs(I), Sr(II) and Eu(III) in smectite rich natural clay, proposed as a backfill material in the Indian geological repository, was studied using the out-diffusion method. Radiotracers (22)Na, (137)Cs, (85)Sr and (154)Eu were used; the first three are carrier-free enabling experimental work at sub-micromolar metal ion concentration, and Eu(III) tracer (154)Eu was used at sub millimolar concentration. An out-diffusion methodology, wherein a thin planar source of radioactivity placed between two clay columns diffuses out, was used to obtain the apparent diffusion coefficient (Da) values. This methodology enabled determination of diffusion coefficient even for strongly sorbing (154)Eu. Da values for (22)Na, (137)Cs, (85)Sr and (154)Eu were 2.35 (±0.14) × 10(-11), 2.65 (±0.09) × 10(-12), 3.32 (±0.15) × 10(-11) and 1.23 (±0.15) × 10(-13) m(2) s(-1), respectively. Da values were found to be in fair agreement with literature data reported for similar mineralogical sediments. Sorption of radionuclides on the clay was also determined in the present study and differences in Da values were rationalized on the basis of sorption data. Distribution ratios (Kd) for Cs(I) and Eu(III) were higher than that for Sr(II), which in turn was higher than that for Na(I). Copyright © 2015 Elsevier Ltd. All rights reserved.

  16. Spectroscopic calculation of the excited electronic states with spin orbit effect of the molecule NaCs

    International Nuclear Information System (INIS)

    Bleik, S.; Korek, M.; Allouche, A.R.

    2004-01-01

    Full text.The existence of new experimental data on the alkali dimers has stimulated theoretical approaches, necessary to provide predictions accurate enough to be useful for interpretation and evenly for guidance of experiments. With the aim of improving the accuracy of predictions we will perform a theoretical study of the electronic structure of the molecule NaCs using a method mainly in the way by which core-valence effects are taken into account. To investigate the electronic structure of NaCs we will use the package CIPSI (Configuration Interaction by Perturbation of a multiconfiguration wave function Selected Interactively) of the Laboratoire de Physique Quantique (Toulouse, France). The atoms Na and Cs will be treated through non-empirical effective one electron core potentials of Durand and Barthelat type. Molecular orbitals for NaCs will be derived from Self Consistent field Calculations (SCF) and full valence Configuration Interaction (IC) calculations. A core-core interaction more elaborated than the usual approximation 1/R will be taken into account as the sum of an exponential repulsive term plus a long range dispersion term approximated by the well known London formula. Potential energy calculations will be performed for different molecular states, for numerous values of the inter-nuclear distance R in a wide range. Spectroscopic constants have been derived for the bound states with regular shape. A ro vibrational study have been performed for the ground states with a calculation of the rotational and centrifugal distortion constants. A calculation for the transition dipole moment and matrix elements have been done for the bound states

  17. Ternary system of Na2MoO4-Cs2MoO4-MoO3

    International Nuclear Information System (INIS)

    Zueva, V.P.; Shabanova, A.N.; Drobasheva, T.I.

    1982-01-01

    Using the methods of thermal analysis interaction of components in ternary system Na 2 MoO 4 -Cs 2 MoO 4 -MoO 3 has been studied. Crystallization surface consists of nine fields belonging to initial components and compounds of lateral sides. Triangulation of the system is carried out and the character of nonvariant points is clarified, the temperature of 360 deg C corresponds to low-melting eutectics

  18. Cu and Zn substituted silicon clathrates with the cubic type-II structure. Synthesis and characterization of Cs{sub 8}Na{sub 16}Cu{sub 3.8}Si{sub 132.2} and Cs{sub 8}Na{sub 16}Zn{sub 6.9}Si{sub 129.1}

    Energy Technology Data Exchange (ETDEWEB)

    Schaefer, Marion C.; Bobev, Svilen [Department of Chemistry and Biochemistry, University of Delaware, Newark, DE (United States)

    2017-12-13

    Studies in the systems Cs-Na-Cu-Si and Cs-Na-Zn-Si yielded the novel clathrates Cs{sub 8}Na{sub 16}(Cu,Si){sub 136} and Cs{sub 8}Na{sub 16}(Zn,Si){sub 136}, both with the cubic type-II structure [space group Fd anti 3m (no. 227), Pearson symbol cF160]. The structures of the title compounds were established from single-crystal X-ray diffraction methods, confirming the complete ordering of the Cs and Na guest atoms. The framework-building Si atoms are found to be randomly substituted by Cu atoms on framework site 96g, exclusively. In the structure of Cs{sub 8}Na{sub 16}(Zn,Si){sub 136}, the refinements indicate that the Zn and Si atoms co-occupy two of the three framework sites with notable preference for site 96g over site 32e. The corresponding refined compositions and unit cell parameters are as follows: Cs{sub 8}Na{sub 16}Cu{sub 3.8}Si{sub 132.2(1)} [a = 14.7583(15) Aa]; Cs{sub 8}Na{sub 16}Zn{sub 6.9}Si{sub 129.1(1)} [a = 14.7682(5) Aa], respectively. The type-II clathrates can be obtained only from experiments employing both Na and Cs, whereas work in the ternary Cs-Cu-Si, Cs-Zn-Si, Na-Cu-Si, and Na-Zn-Si systems failed to yield any clathrate phases. At the same conditions, exploratory studies in the K-Zn-Si and Rb-Zn-Si systems provided evidence that type-I clathrates are favored. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  19. The Cathodic Behavior of Ti(III) Ion in a NaCl-2CsCl Melt

    Science.gov (United States)

    Song, Yang; Jiao, Shuqiang; Hu, Liwen; Guo, Zhancheng

    2016-02-01

    The cathodic behavior of Ti(III) ions in a NaCl-2CsCl melt was investigated by cyclic voltammetry, chronopotentiometry, and square wave voltammetry with a tungsten electrode being the working electrode at different temperatures. The results show that the cathodic behavior of Ti(III) ion consists of two irreversible steps: Ti3+ + e = Ti2+ and Ti2+ + 2 e = Ti. The diffusion coefficient for the Ti(III) ion in the NaCl-2CsCl eutectic is 1.26 × 10-5 cm2 s-1 at 873 K (600 °C), increases to be 5.57 × 10-5 cm2 s-1 at 948K (675°C), and further rises to 10.8 × 10-5 cm2 s-1 at 1023 (750 °C). Moreover, galvanostatic electrolysis performed on a titanium electrode further presents the feasibility of electrodepositing metallic titanium in the molten NaCl-2CsCl-TiCl3 system.

  20. Precipitation behaviors of Cs and Re(/Tc) by NaTPB and TPPCl from a simulated fission products-(Na2CO3-NaHCO3)-H2O2 solution

    International Nuclear Information System (INIS)

    Lee, Eil Hee; Lim, Jae Gwan; Chung, Dong Yong; Yang, Han Beum; Kim, Kwang Wook

    2010-01-01

    In this study, the removal of Cs and Tc from a simulated fission products (FP) solution which were co-dissolved with U during the oxidative-dissolution of spent fuel in a mixed carbonate solution of (Na 2 CO 3 -NaHCO 3 )-H 2 O 2 was investigated by using a selective precipitation method. As Cs and Tc might cause an unstable behavior due to the high decay heat emission of Cs as well as the fast migration of Tc when disposed of underground, it is one of the important issues to removal them in views of the increase of disposal safety. The precipitation of Cs and Re (as a surrogate for Tc) was examined by introducing sodium tetraphenylborate (NaTPB) and tetraphenylphosponium chloride (TPPCl), respectively. Precipitation of Cs by NaTPB and that of Re by TPPCl were completed within 5 minutes. Their precipitation rates were not influenced so much by the temperature and stirring speed even if they were increased by up to 50 .deg. C and 1,000 rpm. However, the pH of the solution was found to have a great influence on the precipitation with NaTPB and TPPCl. Since Mo tends to co-precipitate with Re at a lower pH, especially, it was effective that a selective precipitation of Re by TPPCl was carried out at pH of above 9 without co-precipitation of Mo and Re. Over 99% of Cs was precipitated when the ratio of [NaTPB]/[Cs]>1 and more than 99% of Re, likewise, was precipitated when the ratio of [TPPCl]/[Re]>1.

  1. Solubility relations in the ternary system NaCl-CsCl-H2O at 1 atm. 1. Solubilities of halite from 20 to 100 °C

    Science.gov (United States)

    Chou, I.-Ming; Lee, R.D.

    1983-01-01

    Solubilities of halite in the ternary system NaCl-CsCl-H2O have been determined by the visual polythermal method at 1 atm from 20 to 100??C along five constant CsCl/(CsCl + H2O) weight ratio lines. These five constant weight ratios are 0.1, 0.2, 0.3, 0.4, and 0.5. The maximum uncertainties in these measurements are ??0.02 wt % NaCl and ??0.15??C. The data along each constant CsCl/(CsCl + H2O) weight ratio line were regressed to a smooth curve. The maximum deviation of the measured solubilities from the smooth curves is 0.06 wt % NaCl. Isothermal solubilities of halite were calculated from smoothed curves at 25, 50, and 75??C.

  2. Conductrometric, density and thermal measurements of the M2S2O7 (M = Na, K, Rb, Cs) salts

    DEFF Research Database (Denmark)

    Hatem, Gerard; Abdoun, Fatma; Gaune-Escard, Marcelle

    1998-01-01

    Physico-chemical properties, such as densities, conductivities, enthalpies of phase transitions and melting points, have been measured and summarised for the alkali pyrosulphates Na2S2O7, K2S2O7, Rb2S2O7, CS2S2O7. The densities of the molten pyrosulphates could be expressed by the linear expression...... pyrosulphates the temperatures of fusion, the enthalpies and entropies of fusion and possible solid-solid transitions together with the molar heat capacities of the solid and liquid pyrosulphates at 300-800 K, have been obtained and discussed in relation to the conductrometric measurements and the few related...

  3. Nondestructive analysis of RA reactor fuel burnup, Program for burnup calculation base on relative yield of {sup 106}Ru, {sup 134}Cs and {sup 137}Cs in the irradiated fuel; Nedestruktivno odredjivanje izgaranja goriva reaktora RA, Program za izracunavanje izgaranja na osnovu relativne zastupljenosti {sup 106}Ru, {sup 134}Cs i {sup 137}Cs u ozracenom gorivu

    Energy Technology Data Exchange (ETDEWEB)

    Bulovic, V F [Institute of nuclear sciences Boris Kidric, Vinca, Beograd (Yugoslavia)

    1971-07-01

    Burnup of low enriched metal uranium fuel of the RA reactor is described by two chain reactions. Energy balance and material changes in the fuel are described by systems of differential equations. Numerical integration of these equations is base on the the reactor operation data. Neutron flux and percent of Uranium-235 or more frequently yield of epithermal neutrons in the neutron flux, is determined by iteration from the measured contents of {sup 106}Ru, {sup 134}Cs and {sup 137}Cs in the irradiated fuel. The computer program was written in FORTRAN-IV. Burnup is calculated by using the measured activities of fission products. Burnup results are absolute values. Sagorevanje maloobogacenog uranskog metalnog goriva reaktora RA je opisano dvema lancanim reakcijama. Energetski bilans i materijalne promene u gorivu su opisane sistemima diferencijalnih jednacina. Numericka integracija jednacina se vrsi na osnovu podataka u dinamici rada reaktora. Fluks reaktorskih neutrona i procenat urana-235 ili ucesce epitermalnih neutrona u fluksu, odredjuje se iterativno na osnovu izmerenog sadrzaja {sup 106}Ru, {sup 134}Cs i {sup 137}Cs u ozracenom gorivu. Program je napisan u FORTRAN-u IV u jednom bloku, bez podprograma. Izracunavanje izgaranja je zasnovano na izmerenim kolicnicima aktivnosti fisionih produkata. Rezultati izgaranja imaju apsolutni karakter (author)

  4. Coprecipitation of trace amounts of 137Cs and 85Sr with [Na(18-Crown-6]BPh4 from neutral and alkaline solutions

    International Nuclear Information System (INIS)

    Kulyukhin, S.A.; Konovalova, N.A.; Rumer, I.A.; Kamenskaya, A.N.; Mikheev, N.B.

    2005-01-01

    Coprecipitation of 137 Cs and 85 Sr with [Na(18-crown-6]BPh 4 solid phase from aqueous, aqueous-ethanolic, and alkaline solutions is studied. 137 C s and 85 Sr co-crystallize with [Na(18-crown-6]BPh 4 from aqueous and aqueous-ethanolic solutions. The cocrystallization coefficients D of 137 Cs and 85 Sr from aqueous solutions are 2.6 ± 0.5 and 3.3 ± 0.3, respectively. For aqueous-ethanolic solutions, the corresponding values are 4.4 ± 0.5 and 3.4 ± 0.4. In the alkaline solutions (0.1 and 1 M NaOH), 54-74% of 137 Cs and 37-51% of 85 Sr pass into the [Na(18-crown-6)]BPh 4 solid phase, depending on the crown ether concentration in the system [ru

  5. Phase formation in systems Re-Se-Br-MBr (M=Li, Na, K, Rb, Cs

    International Nuclear Information System (INIS)

    Yarovoj, S.S.; Mironov, Yu.V.; Tkachev, S.V.; Fedorov, V.E.

    2009-01-01

    Phase formation in the systems Re-Se-Br-MBr (M=K, Rb, Cs) has been studied by NMR-spectroscopy and X-ray phase analysis. Polymer complexes Re 6 Se 8 Br 2 and M 2 Re 6 Se 8 Br 4 (M=Cs, Rb), and salts containing cluster anions [Re 6 Se 6 Br 8 ] 2- and [Re 6 Se 7 Br 7 ] 3- are the main products of reactions occurring in molten alkali metal halides in the number of cluster anions [{Re 6 Se 8-n Br n }Br 6 ] (4-n)- (0≤n≤4). Effect of alkali metal cation on the composition and ratios of formed products is established

  6. Systems of Na/sup +/NO/sub 3/, Na/sub 2/SO/sub 4/, RbNO/sub 3/, Rb/sub 2/SO/sub 4/-H/sub 2/O and NaNO/sub 3/, Na/sub 2/SO/sub 4/, CsNO/sub 3/, Cs/sub 2/SO/sub 4/-H/sub 2/O at 25 and 75 deg C

    Energy Technology Data Exchange (ETDEWEB)

    Poletaev, I F; Krasnenkova, L V

    1975-08-01

    Quaternary Na/sup +/, Rb/sup +///NO/sub 3/-, SO/sub 4//sup 2 -/-H/sub 2/O and Nsub(+), Cs/sup +///NO/sub 3/-, SO/sub 4//sup 2 -/-H/sub 2/O mutual systems have been studied isothermally. The following six fields of crystallization have been revealed in these systems at 25 deg C: Cs/sub 2/SO/sub 4/, Na/sub 2/SO/sub 4/, Na/sub 2/SO/sub 4/x10H/sub 2/O, NaNO/sub 3/xNa/sub 2/SO/sub 4/x2H/sub 2/O, NaNO/sub 3/, and CsNO/sub 3/.

  7. Conductivity And Thermal Stability of Solid Acid Composites CsH2PO4 /NaH2PO4/ SiO2

    International Nuclear Information System (INIS)

    Norsyahida Mohammad; Abu Bakar Mohamad; Abu Bakar Mohamad; Abdul Amir Hassan Kadhum

    2016-01-01

    Solid acid composites CsH 2 PO 4 / NaH 2 PO 4 / SiO 2 with different mole ratios of CsH 2 PO 4 and NaH 2 PO 4 to SiO 2 were synthesized and characterized. Preliminary infrared measurements of CsH 2 PO 4 and its composites indicated that hydrogen bonds breaking and formation were detected between 1710 to 2710 cm -1 , while the rotation of phosphate tetrahedral anions occurred between 900 and 1200 cm -1 . The superprotonic transition of CsH 2 PO 4 / NaH 2 PO 4 / SiO 2 composite was identified at superprotonic temperatures between 230 and 260 degree Celcius, under atmospheric pressure. This study reveals higher conductivity values for composites with higher CsH 2 PO 4 (CDP) content. Solid acid composite CDP 613 appeared as the composite with the highest conductivity that is 7.2x10 -3 S cm -1 at 230 degree Celcius. Thermal stability of the solid acid composites such as temperature of dehydration, melting and decomposition were investigated. The addition of NaH 2 PO 4 lowers the dehydration temperature of the solid acid composites. (author)

  8. Application of boat method in emissive flame photometry for determination of Li, Rb, Cs, Na, K, Ca, Sr, Ba

    International Nuclear Information System (INIS)

    Orlov, N.A.; Pobedonostsev, V.A.; Savel'ev, Yu.A.

    1976-01-01

    Study of the flame temperature and dependence of adsorbance on the C/O ratio over the boat for the carbide forming elements and the effect of material, thickness, and the height of the boat on the vaporization of alkaline and alkaline earth metals is described. For a boat (70x8, and 0.3 mm thickness), made from Cu, brass, and Ni, the fall in temperature over the boat was 70, 130, 250, and 340 0 , respectively, for air-C 2 H 2 and 50, 100, 210, and 280 0 for N 2 O-C 2 H 2 flame. Introduction of the boat increases the C/O ratio in the analytical zone of the flame, probably caused by a creation of a shaded space, immediately above the boat. Smaller amounts of atmospheric O enter into the space, when compared with the flame in the absence of the boat. The increase in the C/O ratio decreases the absorbance, which in turn, is caused by the fall in temperature and formation of carbides. Time lag between heating of the boat and the initiation of vaporization of the sample and the duration of evaporation impulse were measured. Solutions of CsCl, containing 1 μg Cs/ml were used at 852.1 nm. The boats, previously treated with 0.1% polystyrene in C 6 H 6 , to give a hydrophobic surface and an uniform salt layer distribution, containing the sample were dried under an ir lamp and introduced into the flame. The dependence of Cs emission on the thickness of the different materials (Ni, Cu, Ta) and heights of boats in the air-C 2 H 2 flame is illustrated. The duration of the emission impulse decreases linearly with the decrease of thickness of the boat for all materials tested. Limits of detection of Na, K, Li, Rb, Cs, Ca, Sr, and Ba were determined by using the equilibrium and the boat methods, the latter being some 1-2 orders lower than the former

  9. Calibration of angle response of a NaI(Tl) airborne spectrometer to 137Cs and 60Co point sources on the ground

    International Nuclear Information System (INIS)

    Liu Xinhua; Zhang Yongxing; Gu Renkang; Shen Ensheng

    1998-01-01

    The angle response function F(φ,θ) is a basic calibration of airborne spectrometers in airborne surveying for nuclear emergency monitoring. The author describes the method and results of angle response function calibration of a NaI(Tl) airborne spectrometer for 137 Cs and 60 Co point sources on the ground, with less than 20% uncertainty. By using the results, the calibration factors of the NaI(Tl) airborne spectrometer fixed in Yun-5 plane at different flying heights are calculated by numerical integral method for 137 Cs uniform area source on ground surface, with less than 25% uncertainty. The minimum detection limits (L D ) are calculated at 90 m and 120 m flying heights in the range of over Shijiazhuang airborne surveying for 137 Cs uniform area source on ground surface to be 3.83 and 5.62 kBq/m 2 , respectively

  10. Vibronic intensities for Er{sup 3+} in Cs{sub 2} NaErCl{sub 6}

    Energy Technology Data Exchange (ETDEWEB)

    Acevedo, R.; Navarro, G. [Departamento de Quimica Basica, Facultad de Ciencias Fisicas y Matematicas, Universidad de Chile, Beauchef 850, Casilla 2777, Santiago (Chile); Meruane, T. [Universidad Metropolitana de Ciencias y Educacion, Av. Jose Pedro Alessandri 774, Casilla 147-C Santiago (Chile)

    2001-07-01

    In this current study, we have undertaken vibronic intensity calculations for the absorptions (({sup 4}I{sub 15/2}) {gamma}{sub k}) {yields} (({sup 4}I{sub 13/2}) {gamma}{sub l}) of the Er{sup 3+} in the Cs{sub 2}NaErCl{sub 6} elpasolite type system. This system is extremely complicated to handle from both a theoretical and an experimental viewpoints. This theoretical work shows that over an energy range of about 400 cm{sup -1}, a substantial amount of transitions are likely to take place (about 100 transitions; twenty five of them are magnetic dipole allowed and seventy five are vibronically allowed). It is then a formidable task to identify and assign all of these transitions in a non-ambiguous way. Also the experimental evidence available for these absorptions is related to a total of about twenty lines in the luminescence spectrum of this system. The spectrum itself is very challenging and the superposition of spectral features is most likely to occur. A careful analysis of the calculated vibronic intensities and overall oscillator strengths for the various transitions indicates that the current model used is both flexible and appropriate to deal with this kind of systems. In a forthcoming paper, we will examine the rather unusual high intensity associated with the (({sup 4}I{sub 15/2}) {gamma}{sub k}) {yields} (({sup 4}S{sub 3/2}) {gamma}{sub l}) excitations. (Author)

  11. Transition probabilities for the alkali isoelectronic sequences Li I, Na I, K I, Rb I, Cs I, FR I

    International Nuclear Information System (INIS)

    Lindgard, A.; Nielsen, S.E.

    1977-01-01

    Dipole transition probabilities, oscillator strengths, lifetimes (mean lives), and branching ratios derived from a numerical Coulomb approximation are presented for experimentally identified (and some extrapolated) states n< or =12, l< or =4 for each of the following members of the alkali sequences (Z/sub net/ is the net charge of the corresponding ion): Li I Z/sub net/=1-15, 17-24 Rb I Z/sub net/=1-6 Na I Z/sub net/=1-24 Cs I Z/sub net/=1-5 K I Z/sub net/=1-7 Fr I Z/sub net/=2,4. The results are presented in transition diagrams and in tables giving energy-level values and transition wavelengths as well. An appendix on hydrogen results for 5< or =n< or =12, 4< or =l< or =11 is included to represent the high-angular-momentum states of all members of the alkali isoelectronic sequences

  12. Spectral intensities in cubic systems. III. The Cs{sub 2}NaEuCl{sub 6} system

    Energy Technology Data Exchange (ETDEWEB)

    Acevedo, R.; Hurtado, O. [Department of Basic Chemistry, Faculty of Physical and Mathematical Sciences, University of Chile. Tupper 2069, Casilla 2777, Santiago, Chile (Chile); Meruane, T. [Department of Chemistry, Universidad Metropolitana de Ciencias de la Educacion. Av. J.P. Alessandri 774, Casilla 147. C. Santiago, Chile (Chile); Navarro, G. [Comision Chilena de Energia Nuclear, La Reina, Amunategui 95, Casilla 188-D, Santiago, Chile (Chile); Diaz, V.; Pozo, J. [Facultad de Ciencias de la Ingenieria, Universidad Diego Portales. Casilla 298-V, Santiago, Chile (Chile)

    1998-12-01

    The optical properties of Cs{sub 2}NaEuCl{sub 6} system are reinvestigated on the basis of new and updated experimental data from Raman, electronic Raman, Infrared absorption and visible luminescence. These experimental studies have enable scientist to identify and assign all of the energy levels and corresponding electronic transitions up to 21500 cm{sup -1}. Furthermore, the crystal field level identification from absorption spectroscopy has been confirmed from the additional emission and electronic Raman studies. We decided to study the most likely intensify mechanisms for this system, based upon these new experimental data and a modified version of a combined vibronic formalism, which takes into account the closure procedure for the intermediate electronic states. The total and relative vibronic intensity distributions are calculated and compared with the experimental data, when available. It is shown that the present calculation model although complex uses a minimum set of adjustable parameters from experimental data. The advantages and disadvantages of our physical models and calculation methods are compared with those of other authors and a full discussion is put forward in this paper. (Author)

  13. Electrochemistry of oxygen-free curium compounds in fused NaCl-2CsCl eutectic

    International Nuclear Information System (INIS)

    Osipenko, A.; Maershin, A.; Smolenski, V.; Novoselova, A.; Kormilitsyn, M.; Bychkov, A.

    2010-01-01

    This work presents the electrochemical study of Cm(III) in fused NaCl-2CsCl eutectic in the temperature range 823-1023 K. Transient electrochemical techniques such as cyclic, differential pulse and square wave voltammetry, and chronopotentiometry have been used in order to investigate the reduction mechanism of curium ions up to the metal. The results obtained show that the reduction reaction takes place in a single step Cm(III)+3e-bar →Cm(0). The diffusion coefficient of [CmCl 6 ] 3- complex ions was determined by cyclic voltammetry at different temperatures by applying the Berzins-Delahay equation. The validity of the Arrhenius law was also verified and the activation energy for diffusion was found to be 44.46 kJ/mol. The apparent standard electrode potential of the redox couple Cm(III)/Cm(0) was found by chronopotentiometry at several temperatures. The thermodynamic properties of curium trichloride have also been calculated.

  14. Experimental absorption and desorption study on a combination of 60Co, 51Cr, 137Cs, 54Mn and 22Na in the carp (Cyprinus carpio L.)

    International Nuclear Information System (INIS)

    Fritsh, A.F.; Baudin, J.P.

    1984-03-01

    The study of radionuclide behavior in water shows that about 25% of the 60 Co et 98% of the 54 Mn are found in particle form, while 96% of the 137 Cs and 87% of the 22 Na remain in solution. The soluble fraction generally remains cationic except for 60 Co, of which over one-fourth becames anionic. The uptake kinetics in the carp vary widely according to the radionuclide. The process is linear for 54 Mn, and tends to decrease in time for 137 Cs, while an equilibrium state tends to avise with 60 Co and 22 Na. The fresh weight concentration factors calculated after 65 days of experimentation were 150, 12, 3 and 120, respectively. Contaminated carp placed in non-radioactive water for 57 days lost between 45% and 65% of the 60 Co, 137 Cs and 54 Mn uptake. These elimination rates correspond to biological half-lives of 70-120 days for radioactive cobalt and cesium, and longer than 120 days for 54 Mn. The process was much more rapid with 22 Na, 95% of which was eliminated in 57 days: this corresponds to two biological half lives of 3 and 15 days. When the fish were deprived of food the process was appreciably slower, but in different proportions for each radionuclide; the effect was more significant for 137 Cs and 60 Co than for 54 Mn and 22 Na. The fecal excretion of radionuclides also diminished: smaller quantities of 60 Co and 54 Mn were eliminated under these conditions than when food was administered. Fecal excretion of 22 Na was practically nil in both cases [fr

  15. Temporal evolution of {sup 137}Cs{sup +}, K{sup +} and Na{sup +} in fruits of South American tropical species

    Energy Technology Data Exchange (ETDEWEB)

    Cid, A.S. [LARA — Laboratório de Radioecologia, Instituto de Física, Universidade Federal Fluminense, Av. Gal Milton Tavares de Souza, s/no, Gragoatá, 24210-340, Niterói, RJ (Brazil); Anjos, R.M., E-mail: meigikos@if.uff.br [LARA — Laboratório de Radioecologia, Instituto de Física, Universidade Federal Fluminense, Av. Gal Milton Tavares de Souza, s/no, Gragoatá, 24210-340, Niterói, RJ (Brazil); Zamboni, C.B. [Instituto de Pesquisas Energéticas e Nucleares (IPEN/CNEN), Av. Lineu Prestes 2242, Cidade Universitária, 05508-000, Paulo, SP (Brazil); Velasco, H. [GEA, Instituto de Matemática Aplicada San Luis (IMASL), Universidad Nacional de San Luis, Consejo Nacional de Investigaciones Científicas y Técnicas. Ej. de los Andes 950, D5700HHW San Luis (Argentina); Macario, K. [LARA — Laboratório de Radioecologia, Instituto de Física, Universidade Federal Fluminense, Av. Gal Milton Tavares de Souza, s/no, Gragoatá, 24210-340, Niterói, RJ (Brazil); Rizzotto, M. [GEA, Instituto de Matemática Aplicada San Luis (IMASL), Universidad Nacional de San Luis, Consejo Nacional de Investigaciones Científicas y Técnicas. Ej. de los Andes 950, D5700HHW San Luis (Argentina); and others

    2013-02-01

    Concentrations of {sup 137}Cs, K and Na in fruits of lemon (Citrus limon B.) and of K and Na in fruits of coconut (Cocos nucifera L.) trees were measured by both gamma spectrometry and neutron activation analysis, with the aim to understand the behaviour of monovalent inorganic cations in tropical plants as well as the plant ability to store these elements. Similar amounts of K{sup +} were incorporated by lemon and coconut trees during the growth and ripening processes of its fruits. The K concentration decreased exponentially during the growth of lemons and coconuts, ranging from 13 to 25 g kg{sup −1} dry weight. The incorporation of Na{sup +} differed considerably between the plant species studied. The Na concentration increased linearly during the lemon growth period (0.04 to 0.70 g kg{sup −1} d.w.) and decreased exponentially during the coconut growth period (1.4 to 0.5 g kg{sup −1} d.w.). Even though radiocaesium is not an essential element to plants, our results have shown that {sup 137}Cs incorporation to vegetable tissues is positively correlated to K distribution within the studied tropical plant species, suggesting that the two elements might be assimilated in a similar way, going through the biological cycle together. A mathematical model was developed from the experimental data allowing simulating the incorporation process of monovalent inorganic cations by the fruits of such tropical species. The agreement between the theoretical approach and the experimental values is satisfactory along fruit development. - Highlights: ► Concentrations of {sup 137}Cs, K and Na in fruits of lemon (Citrus limon B.) are presented. ► Concentrations of K and Na in fruits of coconut (Cocos nucifera L.) are also showed. ► We investigated the use of {sup 137}Cs as a tracer for the plant absorption of macronutrients. ► A model was developed to simulate the temporal evolution of {sup 137}Cs, K and Na by fruits. ► This model exhibited close agreement with our

  16. Thermal ionization and plasma state of high temperature vapor of UO2, Cs, and Na: Effect on the heat and radiation transport properties of the vapor phase

    International Nuclear Information System (INIS)

    Karow, H.U.

    1979-01-01

    The paper deals with the question how far the thermophysical state and the convective and radiative heat transport properties of vaporized reactor core materials are affected by the thermal ionization existing in the actual vapor state. The materials under consideration here are: nuclear oxide fuel (UO 2 ), Na (as the LMFBR coolant material), and Cs (alkaline fission product, partly retained in the fuel of the core zone). (orig./RW) [de

  17. Effects of Cr3+ concentration on the optical properties of Cs2NaAlF6 single crystals

    DEFF Research Database (Denmark)

    S. Pedro, Sandra; P. Sosman, Lilian; B. Barthem, Ricardo

    2013-01-01

    This work is devoted to the study of optical properties of the elpasolite Cs2NaAlF6 with 0.1, 1.0, 3.0, 10.0, 30.0 and 50.0% of Cr3+ ions. The interest in this system lies on the fact that it presents a high quantum yield in the visible and infrared regions and therefore can be considered for las...

  18. Selectivity of crystalline Cesup(IV) phosphate sulphate hydrates for Li+, Na+, K+, Rb+ Cs+, and NH4+ in absolute methanol and absolute dimethylsulphoxide

    International Nuclear Information System (INIS)

    Koenig, K.H.; Psotta, L.

    1978-01-01

    The sequence of exchange capacities of Cerium(IV) phosphate sulphate hydrate (CePO 4 ) 2 (HPO 4 )sub(0.74(SO 4 )sub(0.26) . 4.74 H 2 O for alkalimetal ions and ammoniumions in absolute methanol at 25 0 C for the case of a small excess of the exchanger (in relation to the equivalent amount) is given by K + > Rb + >= NH 4 + > Cs + > Na + > Li + . Between the exchange capacity A of these cations and their ionic radii r (given by Ladd) exists the simple relation A = const./r. For Na + the radius of the inner hydration shell must be considered. In absolute dimethyl-sulphoxide under the same conditions the sequence is K + >= NH 4 + > Rb + > Na + > Cs + > Li + . For K + , NH 4 + , Rb + and Cs + the exchange capacity is given by A = const./r. + const. . r 4 . The sequences of the alkali ions in both solvents are among the group of 13 sequences which are physicaly significant according to Eisenmann's theory. The results are compared with the observations made with water as solvent. (author)

  19. Judd–Ofelt modeling, emission lifetimes and non-radiative relaxation for Er{sup 3+} doped Cs{sub 2}NaYF{sub 6} elpasolite crystals

    Energy Technology Data Exchange (ETDEWEB)

    Loiko, P.A. [ITMO University, 49 Kronverkskiy pr., St. Petersburg 197101 (Russian Federation); Vilejshikova, E.V. [Center for Optical Materials and Technologies (COMT), Belarusian National Technical University, 65/17 Nezavisimosti Ave., Minsk 220013 (Belarus); Khaidukov, N.M. [N.S. Kurnakov Institute of General and Inorganic Chemistry, 31 Leninskii Prospekt, Moscow 119991 (Russian Federation); Méndez-Ramos, J. [Departamento de Física, Universidad de La Laguna, La Laguna 38206, Tenerife (Spain); Mateos, X. [Física i Cristallografia de Materials i Nanomaterials (FiCMA-FiCNA), Universitat Rovira i Virgili (URV), Campus Sescelades, c/ Marcellí Domingo, s/n., Tarragona 43007 (Spain); Yumashev, K.V., E-mail: k.yumashev@tut.by [Center for Optical Materials and Technologies (COMT), Belarusian National Technical University, 65/17 Nezavisimosti Ave., Minsk 220013 (Belarus)

    2017-05-15

    Absorption and emission properties of Er{sup 3+} ions in a cubic elpasolite crystal, Cs{sub 2}NaYF{sub 6}, are modeled within the Judd-Ofelt (J-O) theory. The J-O intensity parameters have been determined: Ω{sub 2} = 0.665, Ω{sub 4} = 0.217 and Ω{sub 6} = 0.029 ×10{sup –20} cm{sup 2}. The elpasolite structure of Cs{sub 2}NaYF{sub 6} containing isolated [YF{sub 6}] polyhedra allows high Er{sup 3+} doping levels up to 100 at% without considerable concentration quenching of luminescence and exceptionally long lifetimes of the excited states (in particular, the radiative lifetimes of the {sup 4}I{sub 13/2} and {sup 4}I{sub 11/2} states are as long as 36.7 ms and 113.4 ms, respectively). It also shows weak non-radiative relaxation. Stimulated-emission cross-sections have been determined for the Er{sup 3+} transitions in Cs{sub 2}NaYF{sub 6} at ~2.7 and ~1.5 μm as well as in the visible spectral range.

  20. Application of the Monte Carlo method for the efficiency calibration of CsI and NaI detectors for gamma-ray measurements from terrestrial samples

    International Nuclear Information System (INIS)

    Baccouche, S.; Al-Azmi, D.; Karunakara, N.; Trabelsi, A.

    2012-01-01

    Gamma-ray measurements in terrestrial/environmental samples require the use of high efficient detectors because of the low level of the radionuclide activity concentrations in the samples; thus scintillators are suitable for this purpose. Two scintillation detectors were studied in this work; CsI(Tl) and NaI(Tl) with identical size for measurement of terrestrial samples for performance study. This work describes a Monte Carlo method for making the full-energy efficiency calibration curves for both detectors using gamma-ray energies associated with the decay of naturally occurring radionuclides 137 Cs (661 keV), 40 K (1460 keV), 238 U ( 214 Bi, 1764 keV) and 232 Th ( 208 Tl, 2614 keV), which are found in terrestrial samples. The magnitude of the coincidence summing effect occurring for the 2614 keV emission of 208 Tl is assessed by simulation. The method provides an efficient tool to make the full-energy efficiency calibration curve for scintillation detectors for any samples geometry and volume in order to determine accurate activity concentrations in terrestrial samples. - Highlights: ► CsI (Tl) and NaI (Tl) detectors were studied for the measurement of terrestrial samples. ► Monte Carlo method was used for efficiency calibration using natural gamma emitting terrestrial radionuclides. ► The coincidence summing effect occurring for the 2614 keV emission of 208 Tl is assessed by simulation.

  1. Radiocesium bioaccumulation in freshwater plankton: Influences of cation concentrations (K+ and Na+) on direct uptake of 137Cs in Chlamydomonas, Scenedesmus and Daphnia. Food-chain transfer of 137Cs from Chlamydomonas to Daphnia at different K+ concentrations

    International Nuclear Information System (INIS)

    Hagstroem, J.

    2002-01-01

    The influences of cation concentrations (K + and Na + ) on radiocesium ( 137 Cs) bioaccumulation in two freshwater phytoplankton species (Scenedesmus quadricauda and Chlamydomonas noctigama) were systematically investigated in batch-cultures monitored during two weeks. Both species were cultured at 9 μE M -2 s -1 constant illumination at 20 deg. C. The exponential growth phase lasted for more than 100 hours (μ ≅ 0.02 h -1 for C. noctigama and 0.03 h -1 for S, quadricauda). Over cation concentration ranges encountered in natural fresh waters ([K + ] from 0.1 μM to 3 mM, [Na + ] from 20 μM to 3 mM), a more than three order of magnitude variation was found for both intake rate and observed bioconcentration factors (BCF) at apparent steady-state (from less than 10 3 to 10 6 L (kg C) -1 ). For both species, the major effector on BCF and uptake rate was external [K + ], which was inversely proportional to these parameters over wide ranges (1-1000 μM for S. quadricauda and 0.1 to 300 μM for C. noctigama). At concentrations above these ranges K + still reduced 137 Cs bio-uptake, but less effectively. A minor influence of external [Na + ] on 137 Cs bioaccumulation was indicated for S. quadricauda, whereas no such influence was significant for C. noctigama. A biphasic pattern for 137 Cs bioaccumulation was discovered in C. noctigama. A rapid 'quasi-steady state' with an effective equilibration time of less than 100 hours was approached during the exponential growth phase. A surge in the uptake occurred when exponential growth ceased, and this pattern was consistent over the range 30 μM to 1.4 mM external [K + ]. Since depletion of external [K + ] was not detected for these treatments, this pattern can only be explained if there are at least two different cellular compartments involved. Although less certain, a second steady-state BCF appeared within two weeks, which seems to be up to one order of magnitude higher than the first. Microcosm experiments with the

  2. Studies on structure and covalence effects on hyperfine interactions of AFeO sub(2) and BFeS sub(2) compounds by Moessbauer spectroscopy (A= Na, Cu, Ag, B= K, Rb, Cs, Na)

    International Nuclear Information System (INIS)

    Taft, C.A.

    1975-01-01

    The compounds AFeO sub(2) and BFeS sub(2) (A = Na, Cu, Ag, B = K, Rb, Cs, Na) were investigated by Moessbauer spectroscopy. The spectra were registered at temperature range from 4.2 sup(0) to 300 sup(0)K and magnetic transitions were observed determining correspondent temperatures by variation of hyperfine field. The electric field gradient of these compounds and perovskite type compounds (Pb sub(1-x) - Ba sub(x)) Zr O sub(3) were calculated and experimental part were determined by perturbed angular correlation, taking in account the effects of covalence, crystal lattice parameters and dipolar contributions. (M.C.K.)

  3. Apparatus for rapid adjustment of the degree of alignment of NMR samples in aqueous media: verification with residual quadrupolar splittings in (23)Na and (133)Cs spectra.

    Science.gov (United States)

    Kuchel, Philip W; Chapman, Bogdan E; Müller, Norbert; Bubb, William A; Philp, David J; Torres, Allan M

    2006-06-01

    NMR spectra of (23)Na(+) and (133)Cs(+) in gelatine in a silicone rubber tube that was stretched to various extents showed remarkably reproducible resonance multiplicity. The relative intensities of the components of the split peaks had ratios, 3:4:3, and 7:12:15:16:15:12:7, respectively, that conformed with those predicted using a Mathematica program. The silicone-rubber tube was sealed at its lower end by a small rubber stopper and placed inside a thick-walled glass tube. Gelatine was injected in solution into the silicone tube and 'set' by cooling below 30 degrees C. A plastic thumb-screw held the silicone tube at various degrees of extension, up to approximately 2-fold. After constituting the gel in buffers containing NaCl and CsCl, both (23)Na and (133)Cs NMR spectroscopy revealed that after stretching the initial single Lorentzian line was split into a well-resolved triplet and a heptet, respectively. This was interpreted as being due to coupling between the electric quadrupoles of the nuclei and the average electric field gradient tensor of the collagen molecules of gelatine; these molecules became progressively more aligned in the direction of the main magnetic field, B(0), of the vertical bore magnet, as the gel was stretched. This apparatus provides a simple way of demonstrating fundamental physical characteristics of quadrupolar cations, some characteristics of gelatine under stretching, and a way to invoke static distortion of red blood cells. It should be useful with these and other cell types, for studies of metabolic and membrane transport characteristics that may change when the cells are distorted, and possibly for structural studies of macromolecules.

  4. Determination of Br, Rb, Cs, Sc and Na in various plant leaves located in an urban park by neutron activation analysis

    International Nuclear Information System (INIS)

    Iqbal, M.Z.; Qadir, M.A.

    1990-01-01

    Br, Rb, Cs, Sc and Na concentrations were determined in different plant species from an urban park at Lahore, Pakistan to determine the effect of airborne emission on roadside ecosystem. Attention was paid to the leaves of Sapindus mukorossis, Alstonia scholaris and Diospyros embryopteris. Different varieties of tissues were found to have different concentration of trace elements when compared with each other. The concentration of trace element deposition was compared with the values reported in literature. Significant pollution was observed. (author) 5 refs.; 1 fig.; 1 tab

  5. Calculation of phase equilibria in the Na2SO4-K2SO4-Cs2SO4-H2O system at 25 deg C

    International Nuclear Information System (INIS)

    Filippov, V.K.; Kalinkin, A.M.; Vasin, S.K.

    1990-01-01

    Calculation results of solubility diagram and water activity in saturated solutions of Na 2 SO 4 -K 2 SO 4 -Cs 2 SO 4 -H 2 O system at 25 deg C are presented. It is shown that for the calculation of quaternary systems one can use the Pitzer equations. Solubility diagram for the system studied is plotted and data on composition and water activity of solutions saturated by two or three solid phases are given. Classification of nonvariant equilibria from the viewpoint of isomorphism of solubility and fusibility diagrams permits to depict the direction of phase processes during isothermal evaporation of water

  6. New alkali metal diphosphates how materials to preserve the security of the environment: CsNaCu(P2O7), Rb2Cu(P2O7) and CsNaCo(P2O7) synthesis and crystal structure determination

    Science.gov (United States)

    Chernyatieva, Anastasiya; Filatova, Alyona; Spiridonova, Dariya; Krivovichev, Sergey

    2013-04-01

    In this work we describe preliminary results of the synthesis and of a crystal-chemical study of synthetic phosphates with transition metals. Due to the increasing requirements for environmental safety specialists from various industries, we are searching for sustainable forms of immobilization of hazardous waste during storage. We are also developing a component-based waste for new materials. In our continued exploratory synthesis of compounds containing transition-metals, we were able to produce the new diphosphate phases CsNaCu(P2O7), Rb2Cu(P2O7) and CsNaCo(P2O7). A crystal chemical study has allowed us to identify new phosphates. Crystals of CsNaCu(P2O7) (Phase 1) is orthorhombic, crystallizes in space group Pmn21, with a = 5.147(8), b = 15.126(2), c = 9.717(2) Å, V = 756.20 Å3, R1 = 0.066 and Rb2Cu(P2O7) (Phase 2) is orthorhombic as well, crystallizes in space group Pmcn, with a = 5.183(8), b = 10.096(1), c = 15.146(3) Å, V = 793.55 Å3, R1 = 0.063, they have been obtained by high-temperature reaction of RbNO3, CsNO3, Cu(NO3)2, NaOH and (NH4)4P2O7. Synthetic crystals of the phosphate of copper and rubidium were studied in detail by us on the structures of Rb2Cu(P2O7) and Rb2Cu3(P2O7)2 - new alkali metal copper diphosphates (CHERNYATIEVA et al., 2008). Here we report the synthesis, the structure and the properties of the title compounds and we compare these phases with the previously discovered K2CuP2O7 (ELMAADI et al., 1995) and CsNaMnP2O7 (HUANG et al., 1998). These structures crystallize in other space groups, although their structures are also based on 2-D layers, formed by P2O7 groups combined with polyhedra of the transition metals (CHERNYATIEVA et al., 2012). A crystal chemical study has allowed us to identify even new diphosphates CsNaCu(P2O7) (Phase 3). Crystals of CsNaCoP2O7 is monoclinic, space group P 21/n, with a = 7,424(2), b = 7,648(1), c = 12,931(3)Å, β = 90,71(2)° , V = 734.2(3) Å3 and R1 = 0.060. The structure is based framework of Co

  7. Magneto-optical measurement of spin-lattice relaxation time in KBr and in the Na and Cs halogenetes and Co++ ion magnetic circular dichroism study in KCl

    International Nuclear Information System (INIS)

    Carvalho, R.A.

    1977-01-01

    A magnetic circular dicroism spectrometer is described, which was used in the following experiments: 1) The spin-lattice relaxation time (T 1 ) for F centers in NaCl, NaBr, CsBr and CsCl, at 1,8 0 K in magnetic fields up to 15000Gs is described. The suitability of the theory of ref. (08) to explain the differences observed for halides of differents alkali ions as well as for different structures is verified proves that the hyperfine interaction is the most important mechanism for this kind of centers. It is also verified that, for temperatures between 6 0 K and 15 0 K, T 1 experimental values fits the theory of ref. (21) reasonably well, for F centers in KBr. This theory us an extension of that of ref. (8). 2) The MCD spectra for KCl:Co ++ and Caf 2 :Co ++ in different magnetic fields up to 56KGs, and in temperature range between 1,8 0 K and 4,2 0 K is obtained. The results are consistent with the assumption that Co ++ centers are intersticial in KCl lattice [pt

  8. Spectral intensities for stoichiometric elpasolites. I. Absorption and emission of Tm+3 in systems of the Cs2NaTmZ6 type

    International Nuclear Information System (INIS)

    Acevedo, R; Poblete, V; Pozo, J; Elgueta, R; Tanner, P.A

    2000-01-01

    Based upon new experimental data for systems such as, Cs 2 NaTmZ 6 , where Z - =Cl - , F - [1-4], we have carried out a thorough study of the mechanistic factors related with the spectral intensities for both the absorptions and the emissions of the Cs 2 NaTmZ 6 system. For the above purposes, we have generalized our previous calculation models, and in this article we show novel results for the emissions 3 H 4 (Γ i )→ 3 F 4 (Γ j ) and for the absorptions 3 H 6 (A 1 )→ 3 F 4 (Γ i ), 1 G 4 (Γ i ), 3 H 5 (Γ i ), with Γ-k(k=i,j)=A 1 ,E,T 1 ,T 2 and Γ 1 =T a 1 , T b 1 , E, T 2 . The effects due to dispersion (essentially, electrostatic in character), details of the short range vibrational force field and Jahn-Teller distortion are discussed in the text. The agreement among experiment and theory is satisfactory and a generalized model with a few number of adjustable parameters is introduced to account for the observed spectral intensities

  9. Redox equilibrium of U4+/U3+ in molten NaCl-2CsCl by UV-Vis spectrophotometry and cyclic voltammetry

    International Nuclear Information System (INIS)

    Nagai, Takayuki; Uehara, Akihiro; Fujii, Toshiyuki; Shirai, Osamu; Yamana, Hajimu; Sato, Nobuaki

    2005-01-01

    In order to investigate the redox equilibrium of uranium ions in molten NaCl-2CsCl, UV-Vis absorption spectro-photometry measurements were performed for U 4+ and U 3+ in molten NaCl-2CsCl at 923 K under simultaneous electrolytic control of their ratio. Prominent absorption bands at 480 and 570 nm were assigned to U 3+ , and their molar absorptivities were determined to be 1,260±42 and 963±32 mol -1 ·l·cm -1 respectively. From the dependence of the rest potential of the melt on the spectrophotometrically determined ratio of [U 4+ ]/[U 3+ ], the standard redox potential of the couple U 4+ /U 3+ at 923 K was determined to be -1.481±0.004 V vs. Cl 2 /Cl - . Cyclic voltammetry measurements were carried out for the couple U 4+ /U 3+ , and the results agreed well with this standard redox potential value. By the results of cyclic voltammetry, a temperature dependence of the standard redox potential was found to be -2.094+6.639 x 10 -4 T (T=823-923K). (author)

  10. Ab initio study of spectroscopic properties of bimetallic molecules MeB (where Me=Li, Na, K, Br, Cs, Fr) using CCSD(T) and MRCI methods

    International Nuclear Information System (INIS)

    Cukovicova, M.; Cernusak, I.

    2010-01-01

    For our study we have chosen a series of diatomic molecules MeB (where Me = Li, Na, K, Rb, Cs, Fr). These molecules present experimentally unknown species, hence we were motivated to predict theoretically potential energy curves, equilibrium bond lengths, harmonic frequencies, constants of anharmonicity, dipole moments and dissociation energies for the ground and low-lying excited states using high level ab initio techniques. Based on previous state averaged MRCI calculations in ANO-S basis set of NaB and KB molecules, we have focused on four lowest-lying electronic states, ground state 3Π and excited states 1Σ+, 1Π and 3Σ+. All four states dissociate to the atoms in ground states 2P1/2(B) and 2S1/2(Me). 3Π, 1Σ+, 1Π and 3Σ+ electronic states we investigated employing CCSD(T) method using relativistic ANO-RCC basis set. Our calculations include scalar relativistic effects via the second order one-component (spin-free) Douglas-Kroll-Hess Hamiltonian. Relativistic effects become remarkable in the case of heavy atoms, hence properties of CsB and FrB molecules may differ from trend of properties in row from LiB to FrB. Spectroscopic properties of particular state were obtained from the analysis of the potential energy curves using VIBROT and DUNHAM programs.

  11. First-principle calculations of the structural, elastic and bonding properties of Cs{sub 2}NaLnCl{sub 6} (Ln=La–Lu) cubic elpasolites

    Energy Technology Data Exchange (ETDEWEB)

    Ma, C.G.; Liu, D.X.; Feng, B.; Tian, Y.; Li, L. [College of Sciences, Chongqing University of Posts and Telecommunications, Chongqing 400065 (China); Brik, M.G., E-mail: mikhail.brik@ut.ee [College of Sciences, Chongqing University of Posts and Telecommunications, Chongqing 400065 (China); Institute of Physics, University of Tartu, Ravila 14C, Tartu 50411 (Estonia); Institute of Physics, Jan Dlugosz University, Armii Krajowej 13/15, PL-42200 Czestochowa (Poland)

    2016-01-15

    For the first time the structural, elastic and bonding properties of 15 elpasolite crystals Cs{sub 2}NaLnCl{sub 6} (Ln denotes all lanthanides from La to Lu) were calculated systematically using the CRYSTAL09 program. Several trends in the variation of these properties in relation to the atomic number Z of the Ln ions were found; in particular, the lattice parameter of these compounds decreases with Z (which can lead to the increased crystal field splittings of the 5d states for the heavier Ln ions), whereas the elastic constants and Debye temperature increase. The degree of covalency of the Ln–Cl chemical bonds is increased toward the end of the lanthanide series. - Highlights: • Structural, elastic and bonding properties of 15 cubic elpasolites Cs{sub 2}NaLnCl{sub 6} (Ln=La,…,Lu) are calculated. • Relations between these quantities and Ln atomic number were found. • Possible correlation between the elastic properties and Stokes shift is proposed.

  12. Application of the Monte Carlo method for the efficiency calibration of CsI and NaI detectors for gamma-ray measurements from terrestrial samples

    Energy Technology Data Exchange (ETDEWEB)

    Baccouche, S., E-mail: souad.baccouche@cnstn.rnrt.tn [UR-MDTN, National Center for Nuclear Sciences and Technology, Technopole Sidi Thabet, 2020 Sidi Thabet (Tunisia); Al-Azmi, D., E-mail: ds.alazmi@paaet.edu.kw [Department of Applied Sciences, College of Technological Studies, Public Authority for Applied Education and Training, Shuwaikh, P.O. Box 42325, Code 70654 (Kuwait); Karunakara, N., E-mail: karunakara_n@yahoo.com [University Science Instrumentation Centre, Mangalore University, Mangalagangotri 574199 (India); Trabelsi, A., E-mail: adel.trabelsi@fst.rnu.tn [UR-MDTN, National Center for Nuclear Sciences and Technology, Technopole Sidi Thabet, 2020 Sidi Thabet (Tunisia); UR-UPNHE, Faculty of Sciences of Tunis, El-Manar University, 2092 Tunis (Tunisia)

    2012-01-15

    Gamma-ray measurements in terrestrial/environmental samples require the use of high efficient detectors because of the low level of the radionuclide activity concentrations in the samples; thus scintillators are suitable for this purpose. Two scintillation detectors were studied in this work; CsI(Tl) and NaI(Tl) with identical size for measurement of terrestrial samples for performance study. This work describes a Monte Carlo method for making the full-energy efficiency calibration curves for both detectors using gamma-ray energies associated with the decay of naturally occurring radionuclides {sup 137}Cs (661 keV), {sup 40}K (1460 keV), {sup 238}U ({sup 214}Bi, 1764 keV) and {sup 232}Th ({sup 208}Tl, 2614 keV), which are found in terrestrial samples. The magnitude of the coincidence summing effect occurring for the 2614 keV emission of {sup 208}Tl is assessed by simulation. The method provides an efficient tool to make the full-energy efficiency calibration curve for scintillation detectors for any samples geometry and volume in order to determine accurate activity concentrations in terrestrial samples. - Highlights: Black-Right-Pointing-Pointer CsI (Tl) and NaI (Tl) detectors were studied for the measurement of terrestrial samples. Black-Right-Pointing-Pointer Monte Carlo method was used for efficiency calibration using natural gamma emitting terrestrial radionuclides. Black-Right-Pointing-Pointer The coincidence summing effect occurring for the 2614 keV emission of {sup 208}Tl is assessed by simulation.

  13. Thermodynamic properties and behaviour of A2[(UO2)(MoO4)2] compounds with A = Li, Na, K, Rb, and Cs

    International Nuclear Information System (INIS)

    Lelet, Maxim I.; Suleimanov, Evgeny V.; Golubev, Aleksey V.; Geiger, Charles A.; Depmeier, Wulf; Bosbach, Dirk; Alekseev, Evgeny V.

    2014-01-01

    Highlights: • Low temperature heat capacity of A 2 [(UO 2 )(MoO 4 ) 2 ] (A = Li, Na, K, Rb, and Cs) series was determined. • Enthalpy of formation of Li 2 [(UO 2 )(MoO 4 ) 2 ] was determined by HF solution calorimetry. • Δ f G° (T = 298 K) of all phases from studied series were calculated. - Abstract: A thermodynamic investigation of five alkali-metal uranyl molybdates of the general formula A 2 [(UO 2 )(MoO 4 ) 2 ], where A = Li, Na, K, Rb, and Cs, was undertaken. The various phases were synthesized by solid-state reaction of ANO 3, with A = Li, Na, K, Rb, or Cs, MoO 3 and γ-UO 3 . The synthetic products were characterized by X-ray powder diffraction and X-ray fluorescence methods. The low-temperature heat capacity, S r °, was measured using adiabatic calorimetry from T = (6 to 335) K. Based on these data, the third law entropy at T = 298.15 K, S°, is (345 ± 1) J · K −1 · mol −1 for Li 2 [(UO 2 )(MoO 4 ) 2 ], (373 ± 1) J · K −1 · mol −1 for Na 2 [(UO 2 )(MoO 4 ) 2 ], (390 ± 1) J · K −1 · mol −1 for K 2 [(UO 2 )(MoO 4 ) 2 ], (377 ± 1) J · K −1 · mol −1 for Rb 2 [(UO 2 )(MoO 4 ) 2 ] and (394 ± 1) J · K −1 · mol −1 for Cs 2 [(UO 2 )(MoO 4 ) 2 ]. The enthalpy of formation of Li 2 [(UO 2 )(MoO 4 ) 2 ] was determined using HF solution calorimetry giving Δ f H°(T = 298 K, Li 2 [(UO 2 )(MoO 4 ) 2 ], cr) = −(3456 ± 9) kJ · mol −1 . Using these new experimental results, together with literature data, the Gibbs free energy of formation of each compound was calculated, giving: Δ f G°(T = 298 K, Li 2 [(UO 2 )(MoO 4 ) 2 ], cr) = −(3204 ± 9) kJ · mol −1 , Δ f G°(T = 298 K, Na 2 [(UO 2 )(MoO 4 ) 2 ], cr) = −(3243 ± 2) kJ · mol −1 , Δ f G°(T = 298 K, K 2 [(UO 2 )(MoO 4 ) 2 ], cr) = −(3269 ± 3) kJ · mol −1 , Δ f G°(T = 298 K, Rb 2 [(UO 2 )(MoO 4 ) 2 ], cr) = −(3262 ± 3) kJ · mol −1 , and Δ f G°(T = 298 K, Cs 2 [(UO 2 )(MoO 4 ) 2 ], cr) = −(3259 ± 3) kJ · mol −1 . Smoothed S r °(T) values

  14. Spectroscopic study of divalent copper complexes forming in the systems CuCl2-MCl (M= Na, K, Rb, Cs)

    International Nuclear Information System (INIS)

    Utorov, N.P.; Bakshi, Yu.M.; Bazov, V.P.; Gel'bshtejn, A.I.

    1982-01-01

    The structure of complex ions formed in salt systems CuCl 2 -MCl depending on the nature of cation of alkali metal chloride at different mole ratios (n=MCl/CuCl 2 ) is studied. The data obtained using the methods of oscillation and electron spectroscopy enable to consider that during the melting of CuCl 2 and CsCl at n 4 2- ions, have the symmetry Csub(2v) at n=1. π-bonding, which is realized with participation of of Cl - p-orbitals and Cu 2+ d-orbitals plays a very important role in the formation of dimers and polymer chains. π-conjugated systems are characterized by the spectrum of charge transfer in the visible region. Charge transfer promotes metal reduction in the excited state which is adequate to the change of electron configuration of copper from d 9 for d 10 . It results in the decrease of acceptor and increase of dative ability of copper cation in the composition of salt complex. Big (n >= 2) additions of CsCl lead to the formation of separate stable ions of CuCl 4 2- type with the symmetry Dsub(2d)

  15. Spectral intensities: The emission spectra for the Cs2NaScCl6: MoCl63- system in the Fm3m space group

    International Nuclear Information System (INIS)

    Acevedo, R.; Meruane, T.; Navarro, G.

    2000-01-01

    Taking advantage of the data reported by Flint and Paulusz, we have undertaken a theoretical investigation of the intensity mechanism for the various emissions; Γ 8 ( 2 T 2g ) → Γ 8 ( 4 A 2g ), Γ 8 ( 2 E g ), Γ 8 ( 2 T 1g ), Γ 6 ( 2 T 1g ) for the Cs 2 NaScCl 6 :MoCl 6 3- system in the Fm3m-space group. The experimental data reported by these authors, refer to the visible and near infrared luminescence spectra of MoCl 3- 6 complex ion in different host, such as Cs 2 NaMCl 6 (M = Sc, Y, In), measured between 15,000 cm -1 and 3,000 cm -1 at liquid helium temperatures. At least, five luminescence transitions have been identified and assigned and each of them show extensive vibronic structure, which was analyzed to yield the vibrational frequencies of the MoX 3- 6 (X -1 = Cl -1 Br -1 ) ion in each excitation. A careful analysis of the experimental data reported shows that for the various observed electronic transitions, the vibration frequencies do change only slightly, and therefore there is no indication that the system undergoes a Jahn-Teller distortion (along an active coordinate) of some importance to be taken into account in the current work. There is, though clear evidence that for the chloro-elpasolites, there is a strong resonance interaction between ν 3 (τ 1u : stretching) of the MoX 6 3- , complex ion and that of the host when M = In, Y. Thus for M = Sc, the slighter higher host ν 3 , wavenumber is likely to minimizes the effect of this coupling. This experimental evidence, will allow us for the Cs 2 NaScCl 6 3- system to neglect to first order approximation, the coupling among the internal and the external vibrations and to proceed using a both a molecular model and the independent system model (ISM)

  16. Hydrogen storage of type MBH{sub 4}(H{sub 2})n M = Li, Na, K, Rb, Cs; Almacenadores de hidrogeno del tipo MBH{sub 4}(H{sub 2})n M = Li, Na, K, Rb, Cs

    Energy Technology Data Exchange (ETDEWEB)

    Sanchez-Castro, Maria Esther [Centro de Investigacion y de Estudios Avanzados del IPN, Unidad Saltillo, Ramos Arizpe, Coahuila (Mexico)] e-mail: esther.sanchez@cinvestav.edu.mx; Sanchez-Vazquez, Mario [Centro de Investigacion en Materiales Avanzados, S.C., Apodaca, Nuevo Leon (Mexico)

    2009-09-15

    Interest has recently been increasing in finding new sources of energy other than fossil fuels. Hydrogen has potential with respect to oil, it does not contaminate the environment or produce greenhouse gases. Nevertheless, finding materials capable of storing hydrogen is not trivial, since certain aspects must be addressed, such as reversible hydrogen storage with high gravimetric and volumetric density, manipulated at moderate temperatures and pressures. To contribute to the search for new materials, we are interested in studying the structures of type MBH{sub 4}, which have a boron atom and a M metal. The boron has a lighter mass and is surrounded by four hydrogen atoms. LiBH{sub 4}, for example, is already being used as a source of hydrogen by disassociating the B-H bonds. On the other hand, the M atom is positive and can house molecular hydrogen in its coordination sphere. Our studies, using mp{sup 2}/def2-TZVP computational methods, show that this type of structures (MBH4) can coordinate in the M atom from three (when M = Li) to nine (when M = Cs) hydrogen molecules. [Spanish] Recientemente, el interes por encontrar nuevas fuentes de energia diferentes al combustible fosil ha ido en aumento. El hidrogeno tiene un potencial con respecto al petroleo, no contamina el medio ambiente ni produce gases invernadero. Sin embargo, encontrar materiales capaces de almacenar hidrogeno no es trivial, ya que se deben cuidar aspectos como: almacenar reversiblemente hidrogeno con alta densidad gravimetrica y volumetrica, y manipularlos a temperaturas y presiones moderadas. A fin de contribuir con la busqueda de nuevos materiales, es de nuestro interes estudiar a las estructuras del tipo MBH4. Estas estructuras tienen la caracteristica de tener un atomo de boro y un metal M. El boro es de masa ligera y esta rodeado de cuatro atomos de hidrogeno. El LiBH{sub 4} por ejemplo ya se esta utilizando como fuente de hidrogenos al disociar los enlaces B-H. Por otra parte, el atomo M es

  17. Particularities of optical pumping effects in cold and ultra-slow beams of Na and Cs in the case of cyclic transitions

    KAUST Repository

    Bruvelis, M.; Cinins, A.; Leitis, A.; Efimov, D. K.; Bezuglov, N. N.; Chirtsov, A. S.; Fuso, F.; Ekers, Aigars

    2015-01-01

    The time-dependent population dynamics of hyperfine (HF) levels of n2p3/2 states is examined for cyclic transitions in alkali atoms. We study a slow and cold atomic beam of Na (n = 3) and Cs (n = 6), taking into account the long interaction time of light with atoms (~200 μs) inside the resonant laser beam. Simple analytical expressions for the populations of the excited states and for the intensities of the absorption lines are derived for a three-level system model. We show that at moderate pump laser power the mixing of HF levels is sufficient to form a flow of population from a cyclic transition to partially open transitions. We discuss various phenomena associated with the evolution of optical pumping that cannot be explained by general analysis of two-level system model.

  18. Selectivity of crystalline Ce(IV)-phosphate-sulphate hydrates for Li+, Na+, K+, Rb+, Cs+, and NH4+ in aqueous medium

    International Nuclear Information System (INIS)

    Koenig, K.H.; Psotta, L.

    1978-01-01

    The sequence of exchange-capacities of Cerium(IV)-phosphate-sulphate hydrate (CePO 4 ) 2 (HPO 4 )sub(0.74)(SO 4 )sub(0.26) . 4.74 H 2 O concerning the alkaline ions and the ammonium ion in water at 25 0 C for the case of a small excess of the exchanger (in relation to the equivalent amount) is given by Na + > K + > Rb + > NH 4 + > Cs + > Li + . The simple relation A const/r was found between the exchange-capacity A of these cations and their ionic radii r (given by Ladd); only for Li + the radius of the inner hydration-shell must be considered. The observations are consistent with Eisenmann's theory. (author)

  19. Solubilities, densities and refractive indices for the ternary systems ethylene glycol + MCl + H2O (M = Na, K, Rb, Cs) at (15 and 35) deg. C

    International Nuclear Information System (INIS)

    Zhou Yanhong; Li Shuni; Zhai Quanguo; Jiang Yucheng; Hu Mancheng

    2010-01-01

    The solubilities, densities and refractive indices data for the four ternary systems ethylene glycol + MCl + H 2 O (M = Na, K, Rb, Cs) at different temperatures were measured, with mass fractions of ethylene glycol in the range of 0 to 1.0. In all cases, the presence of ethylene glycol significantly reduces the solubility of the salts in aqueous solution. The experimental data of density, refractive index and solubility of saturated solutions for these systems were correlated using polynomial equations as a function of the mass fraction of ethylene glycol. On the other hand, the refractive index and density of unsaturated solutions was also determined for the four ternary systems with varied unsaturated salt concentrations. Values for both the properties were correlated with the salt concentrations and proportions of ethylene glycol in the solutions.

  20. Particularities of optical pumping effects in cold and ultra-slow beams of Na and Cs in the case of cyclic transitions

    KAUST Repository

    Bruvelis, M.

    2015-12-09

    The time-dependent population dynamics of hyperfine (HF) levels of n2p3/2 states is examined for cyclic transitions in alkali atoms. We study a slow and cold atomic beam of Na (n = 3) and Cs (n = 6), taking into account the long interaction time of light with atoms (~200 μs) inside the resonant laser beam. Simple analytical expressions for the populations of the excited states and for the intensities of the absorption lines are derived for a three-level system model. We show that at moderate pump laser power the mixing of HF levels is sufficient to form a flow of population from a cyclic transition to partially open transitions. We discuss various phenomena associated with the evolution of optical pumping that cannot be explained by general analysis of two-level system model.

  1. The pentasulfates A{sub 2}[S{sub 5}O{sub 16}] (A = Li, Na, Cs, Ag). Rare species by reactions in SO{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Schindler, Lisa Verena; Struckmann, Mona; Becker, Anna; Wickleder, Mathias S. [Institute of Inorganic and Analytical Chemistry, Justus Liebig University of Giessen (Germany)

    2017-02-03

    The reaction of various sulfate salts A{sub 2}SO{sub 4} (A = Li, Na, Ag, Cs) with neat SO{sub 3} led to the respective pentasulfates A{sub 2}[S{sub 5}O{sub 16}] {Li_2[S_5O_1_6]: monoclinic, C2/c, Z = 4, a = 1850.71(7) pm, b = 665.45(2) pm, c = 992.80(4) pm, β = 106.764(2) , V = 1170.72(7) x 10"6 pm"3; Na_2[S_5O_1_6]: orthorhombic, Pbcn, Z = 4, a = 880.17(3) pm, b = 1039.88(4) pm, c = 1348.58(5) pm, V = 1234.32(8) x 10"6 pm"3; Ag_2[S_5O_1_6]: orthorhombic, Pbcn, Z = 4, a = 884.34(4) pm, b = 1043.19(5) pm, c = 1381.83(7) pm, V = 1274.8(1) x 10"6 pm"3; Cs_2[S_5O_1_6]: monoclinic, P2_1, Z = 4, a = 892.96(3) pm, b = 859.72(3) pm, c = 978.30(4) pm, β = 101.443(2) , V = 736.11(5) x 10"6 pm"3}. All four compounds are colorless and extremely moisture-sensitive substances. They all contain the pentasulfate anion [S{sub 5}O{sub 16}]{sup 2-} that has, until now, only been reported once. This comparative study of polysulfate salts with the same polysulfate anion, but varying countercations, is a crucial step in comprehending this very basic and, nevertheless, poorly investigated class of materials. Raman spectroscopy and powder diffraction complete the structural investigations. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  2. Spectroscopic studies, theoretical models and structural characterization. II. Synthesis and X-ray powder diffraction of the elpasolites Cs2NaSmCl6

    International Nuclear Information System (INIS)

    Poblete, V.; Acevedo, R.

    1998-01-01

    In this research work, we report the synthesis and structural characterization of the stoichiometric elpasolite Cs 2 NaSmCl 6 . The synthesis was performed under a solid state reaction in nitrogen atmosphere from the chemicals CsCl, NaCl and SmCl 3 weighted stoichiometrically. The best possible crystallization temperature was obtained using thermal studies of the type DTA/TGA (the thermal treatment was allowed to proceed for 2.5 hours at 755 Centigrade, showing a temperature gradient of 10 Centigrade/minute). The structural characterization by powder X-ray diffraction (XDR) indicates that this elpasolite belongs to the Fm 3m (O h 5 ) space group and the optimized structural parameters are as follows: a 0 = 10.8342 Armstrong, V 1271.72 Armstrong 3 , Z=4, M=651.88, D x =3.406 y D exp=3.41 ± 0.01. The profile refinement, using the Rietveld method, allowed us to fit the experimental and the calculated intensities of a total of 32 lines. The above result indicates that the condition R exp 2+ + 3Cl -1 and the counter ions filling the octahedral holes, in full agreement with anti fluorite type crystal. According to the above description, these elpasolite adopt the form (M 1/3 □ 2/3 ) 4 X 2 , where M labels the central metal, X stand for the chlorine ions and □ represent the vacancies, which may accommodate a significant amount of defects without collapsing. This experimental study provides the necessary input to test theoretical models against experimental data. (Author)

  3. Effects of administration of potassium- and sodiumchlorides on faecal excretions and salivary and alimentary concentrations of, Na, K, 134Cs, Ca, Mg and P in reindeer fed a lichen diet

    Directory of Open Access Journals (Sweden)

    Hans Staaland

    1998-02-01

    Full Text Available A comparison of the effects of administration of 350 mmol d-1 of KC1 or NaCl on faecal excretions, salivary concentrations and concentrations and pools of Na, K, 134Cs, Ca, Mg, P, and water in the alimentary tract of reindeer was carried out using three groups of three 10 months old reindeer fed a lichen diet. One group was used as a control group with no mineral supplementation. The level of K supplementation mimicked K intakes from summer pastures. NaCl was given at a rate which would mimic intake from salt licks by domestic ruminants of similar body size. Treatment with KC1 increased the salivary and alimentary concentrations and the alimentary pool sizes of K and faecal excretion of K increased. A decrease in l34Cs concentrations in all parts of the gastrointestinal tract indicated greater absorption of 134Cs during the KC1 treatment than in NaCl treated and control animals. Increased intake of Na or K had no significant effect on the digestibility of the lichen diet, but urine production increased. Little effects on pools or concentrations of Ca, Mg and P were observed. NaCl treatment increased urinary and faecal excretion of Na, but did not affect the metabolism of any of the other studied minerals.

  4. Variable dimensionality and framework found in a series of quaternary zinc selenites, A2Zn3(SeO3)4·xH2O (A = Na, Rb, and Cs; 0≤x≤1) and Cs2Zn2(SeO3)3·2H2O

    Science.gov (United States)

    Lü, Minfeng; Jo, Hongil; Oh, Seung-Jin; Ok, Kang Min

    2017-01-01

    Five new alkali metal zinc selenites, A2Zn3(SeO3)4·xH2O (A = Na, Rb, and Cs; 0≤x≤1) and Cs2Zn2(SeO3)3·2H2O have been synthesized by heating a mixture of ZnO, SeO2 and A2CO3 (A = Na, Rb, and Cs), and characterized by X-ray diffraction (XRD) and spectroscopic analyses techniques. All of the reported materials revealed a rich structural chemistry with different frameworks and connection modes of Zn2+. While Rb2Zn3(SeO3)4 and Cs2Zn3(SeO3)4·H2O revealed three-dimensional frameworks consisting of isolated ZnO4 tetrahedra and SeO3 polyhedra, Na2Zn3(SeO3)4, Cs2Zn3(SeO3)4, and Cs2Zn2(SeO3)3·2H2O contained two-dimensional [Zn3(SeO3)4]2- layers. Specifically, whereas isolated ZnO4 tetrahedra and SeO3 polyhedra are arranged into two-dimensional [Zn3(SeO3)4]2- layers in two cesium compounds, circular [Zn3O10]14- chains and SeO3 linkers are formed in two-dimensional [Zn3(SeO3)4]2- layers in Na2Zn3(SeO3)4. Close structural examinations suggest that the size of alkali metal is significant in determining the framework geometry as well as connection modes of transition metal cations.

  5. Variable dimensionality and framework found in a series of quaternary zinc selenites, A2Zn3(SeO3)4·xH2O (A = Na, Rb, and Cs; 0≤x≤1) and Cs2Zn2(SeO3)3·2H2O

    International Nuclear Information System (INIS)

    Lü, Minfeng; Jo, Hongil; Oh, Seung-Jin; Ok, Kang Min

    2017-01-01

    Five new alkali metal zinc selenites, A 2 Zn 3 (SeO 3 ) 4 ·xH 2 O (A = Na, Rb, and Cs; 0≤x≤1) and Cs 2 Zn 2 (SeO 3 ) 3 ·2H 2 O have been synthesized by heating a mixture of ZnO, SeO 2 and A 2 CO 3 (A = Na, Rb, and Cs), and characterized by X-ray diffraction (XRD) and spectroscopic analyses techniques. All of the reported materials revealed a rich structural chemistry with different frameworks and connection modes of Zn 2+ . While Rb 2 Zn 3 (SeO 3 ) 4 and Cs 2 Zn 3 (SeO 3 ) 4 ·H 2 O revealed three-dimensional frameworks consisting of isolated ZnO 4 tetrahedra and SeO 3 polyhedra, Na 2 Zn 3 (SeO 3 ) 4 , Cs 2 Zn 3 (SeO 3 ) 4 , and Cs 2 Zn 2 (SeO 3 ) 3 ·2H 2 O contained two-dimensional [Zn 3 (SeO 3 ) 4 ] 2- layers. Specifically, whereas isolated ZnO 4 tetrahedra and SeO 3 polyhedra are arranged into two-dimensional [Zn 3 (SeO 3 ) 4 ] 2- layers in two cesium compounds, circular [Zn 3 O 10 ] 14- chains and SeO 3 linkers are formed in two-dimensional [Zn 3 (SeO 3 ) 4 ] 2- layers in Na 2 Zn 3 (SeO 3 ) 4 . Close structural examinations suggest that the size of alkali metal is significant in determining the framework geometry as well as connection modes of transition metal cations. - Graphical abstract: Variable dimensions and frameworks were found in a series of quaternary zinc selenites, A 2 Zn 3 (SeO 3 ) 4 (A = Na, Rb and Cs). - Highlights: • Five novel quaternary zinc selenites are synthesized. • All the selenites with different structures contain polarizable d 10 and lone pair cations. • The size of alkali metal cations is significant in determining the framework geometry.

  6. First-principles study of electronic and optical properties of lead-free double perovskites Cs2NaBX6 (B = Sb, Bi; X = Cl, Br, I)

    Science.gov (United States)

    Zhao, Shuai; Yamamoto, Kumiko; Iikubo, Satoshi; Hayase, Shuzi; Ma, Tingli

    2018-06-01

    Organolead halide perovskite is regarded as the most promising light-harvesting material for next-generation solar cells; however, the intrinsic instability and toxicity of lead are still of great concern. Bismuth is ecofriendly and has electronic properties similar to those of lead, which has gradually attracted interest for optoelectronic applications. However, the valence state of bismuth is different from that of lead, eliminating the possibility of replacing lead by bismuth in organolead halide perovskites. To address this matter, one feasible strategy is to construct B-site double perovskites by the combination of Bi3+ and B+ in 1:1 ratio. In this work, lead-free halide double perovskites of the form Cs2NaBX6 (B = Sb, Bi; X = Cl, Br, I) were investigated by first-principles calculations. The electronic properties, optical absorption coefficients, and thermodynamic stability of these compounds were investigated to ascertain their potential application in solar energy conversion. The results provide theoretical support for the exploration of lead-free perovskite materials in potential optoelectronic applications.

  7. X-Ray powder diffraction analysis: Synthesis and spectroscopic studies on the stoichiometric elpasolite Cs2NaTmCl6

    International Nuclear Information System (INIS)

    Acevedo, R.; Poblete, V.; Elgueta, R.; Pozo, J.

    2000-01-01

    The elpasolite Cs 2 NaTmCl 6 belonging to the spatial group Fm3m, has been synthesized and characterized by powder DRX and spectroscopic studies. The synthesis was carried out by means of a solid state reaction at 802.9 o C, for two hours, with a temperature gradient of 4 o C/min. and 2 o C/min, at the beginning and end of the reaction, respectively. The optimum crystallization temperature occurs between 764.5 o C and 838.5 o C. The following crystallographic parameters were obtained: a 0 = 10,6866 o A, V =1220,45( o A) 3 , Z = 4, M = 802.90, D x =3,65 y D exp =3,67. The 32 experimental lines that were analyzed show great accuracy considering that R exp less than R wp . The Raman spectrums allowed for precise identification and assignation so that we can make progress in calculating the crystal dynamics and mechanistic aspects, still unexplored in the literature (C.W)

  8. Synthesis, X-Ray powder diffraction and luminescence spectrum of the Cs2NaYCl6:SmCl63-

    International Nuclear Information System (INIS)

    Acevedo, R.; Meruane, T.; Hurtado, O.F.; Poblete, V; Pozo, J.

    2000-01-01

    The synthesis, structural characterization and a theoretical investigation of the spectral intensities of the emissions Γ( 4 G 5/2 )→ 6 H 9/2 ( b Γ 8 , a Γ 8 , Γ 6 ), 6 H 7/2 (Γ 7 , Γ 8 , Γ 6 ) and 6 H 5/2 (Γ 8 , Γ 6 ) in the Cs 2 NaYCl 6 : SmCl 3- 6 system in undertaken. The experimental evidence indicates, that below 100K, the site symmetry of SmCl 3- 6 in the neat elpasolite undergoes a descent of symmetry, following the group-subgroup chain O h include C 4h , and thus the degeneracy of the G 8 luminescent energy levels is lifted, being the observed splitting of about 4 cm -1 . We have decided to re investigate this system, starting from a rather different though complementary viewpoint and set up a theoretical formalism to study the observed overall and relative vibronic intensity distribution, using a minimum set of parameters to be fitted from the experimental data. Our current work, being reported in this paper may be used for future experimental and theoretical studies in the elpasolsite type systems, in particular full lattice dynamic calculations which may be used to move the state of the art in this complex field of research

  9. Trabalho, cotidiano e arte: uma síntese embasada na Estética de Georg Lukács

    Directory of Open Access Journals (Sweden)

    Deribaldo Santos

    Full Text Available Resumo A partir de uma análise imanente, esta comunicação dialoga com a Estética de Lukács, apresentando algumas das principais categorias utilizadas por esse filósofo para edificar uma nova proposta sobre o campo estético. A tese central do autor considera que a arte partilha de uma condição especial da relação objeto-sujeito, em que a produção de um determinado campo homogêneo, pelo artista, lapida as opacidades da vida cotidiana, possibilitando a elevação do ser social a um patamar superior de objetivação, soerguendo a humanidade à condição de registrar sua autoconsciência. A arte, com essa elevação, comprova a imanência humana. Para desenvolver essa investigação, o autor procura identificar, com base nas mediações obtidas a partir da centralidade do trabalho, os tipos de reflexos existentes na vida cotidiana e como alguns desses reflexos se desenvolvem e se diferenciam dos demais até atingirem determinado grau de objetividade superior.

  10. Synthesis, single-crystal structure determination and Raman spectra of the tricyanomelaminates NaA{sub 5}[C{sub 6}N{sub 9}]{sub 2} . 4 H{sub 2}O (A = Rb, Cs)

    Energy Technology Data Exchange (ETDEWEB)

    Reckeweg, Olaf; DiSalvo, Francis J. [Cornell Univ., Ithaca, NY (United States). Baker Lab.; Schulz, Armin [Max-Planck-Institut fuer Festkoerperforschung, Stuttgart (Germany)

    2016-07-01

    Transparent colorless crystals of NaA{sub 5}[C{sub 6}N{sub 9}]{sub 2} . 4 H{sub 2}O (A = Rb, Cs) were obtained by blending aqueous solutions of Na{sub 3}[C{sub 6}N{sub 9}] and RbF or CsF, respectively, and subsequent evaporation of the water under ambient conditions. Both compounds crystallize in the space group P2{sub 1}/m (no. 11) with the cell parameters a = 815.56(16), b = 1637.7(4) and c = 1036.4(3) pm, and β = 110.738(12) for NaRb{sub 5}[C{sub 6}N{sub 9}]{sub 2} . 4 H{sub 2}O and a = 843.32(6), b = 1708.47(11) and c = 1052.42(7) pm, and β = 112.034(2) for NaCs{sub 5}[C{sub 6}N{sub 9}]{sub 2} . 4 H{sub 2}O, respectively. Raman spectra of the title compounds complement our results.

  11. {sup 137}Cs as tracer of the origin of allochthonous sediments in the Southeast Continental Margin of Brazil; {sup 137}Cs como tracador da origem de sedimentos aloctones na Margem Continental Sudeste do Brasil

    Energy Technology Data Exchange (ETDEWEB)

    Ferreira, Paulo A.L.; Mahiques, Michel M.; FIgueira, Rubens C.L., E-mail: paulo.alves.ferreira@usp.br, E-mail: mahiques@usp.br, E-mail: rfigueira@usp.br [Universidade de Sao Paulo (IO/USP), SP (Brazil). Instituto Oceanografico; Franca, Elvis J., E-mail: ejfranca@cnen.gov.br [Centro Regional de Ciencias Nucleares do Nordeste (CRCN-NE/CNEN-PE), Recife, PE (Brazil)

    2015-07-01

    The distribution of {sup 137}Cs, artificial radionuclide for which there is no current source, can inform on the origin and destination of sediments. This study analyzed about 60 samples of surface sediment to generate a model of spatial distribution of {sup 137}Cs in the Southeast Continental Margin of Brazil and surroundings for evaluating possible sediment sources for this region. The model showed that the levels of {sup 137}Cs in the southern compartment of the Southeast Brazilian Margin (south of Sao Sebastiao Island) are statistically similar to those of the Rio de la Plata river mouth region, indicating sediment entry due to the seasonal intrusion of the plume of Rio de la Plata, a phenomenon already studied by other authors.

  12. Estimation of enthalpies and entropies of melting of arsenates from phase diagrams of MeAsO3-Me3AsO4 (Me=Na,K,Rb,Cs) and correlation of thermodynamic properties of alkali metal arsenates

    International Nuclear Information System (INIS)

    Kasenov, B.K.; Isabaev, S.M.; Buketov, E.A.

    1982-01-01

    Values of ΔHsub(melting)sup(0) and ΔSsub(melting)sup(0) for Na 3 AsO 4 , K 3 AsO 4 , Rb 3 AsO 4 and Cs 3 AsO 4 (65.3 kJ/mol and 44.4 J/molxK respectively) were calculated by the Shredder-Vant-Hoff equation in the approximation of ideal solutions from diagrams of the state of MeAsO 3 -He 3 AsO 4 (Me=Na, K, Rb, Cs) systems. ΔHsub(298)sup(0)-f(Tsub(melting)) and ΔHsub(melting)sup(0)-f(ΔHsub(298)sup(0)) dependences were found for arsenates

  13. Structural diversities induced by cation sizes in a series of fluorogermanophosphates: A2[GeF2(HPO4)2] (A = Na, K, Rb, NH4, and Cs).

    Science.gov (United States)

    Chen, Zhang-Gai; Huang, Xia; Zhuang, Rong-Chuan; Zhang, Yu; Liu, Xin; Shi, Tao; Wang, Shuai-Hua; Wu, Shao-Fan; Mi, Jin-Xiao; Huang, Ya-Xi

    2017-09-12

    Germanophosphates, in comparison with other metal phosphates, have been less studied but potentially exhibit more diverse structural chemistry with wide applications. Herein we applied a hydro-/solvo-fluorothermal route to make use of both the "tailor effect" of fluoride for the formation of low dimensional anionic clusters and the presence of alkali cations of different sizes to align the anionic clusters to control the overall crystal symmetries of germanophosphates. The synergetic effects of fluoride and alkali cations led to structural changes from chain-like structures to layered structures in a series of five novel fluorogermanophosphates: A 2 [GeF 2 (HPO 4 ) 2 ] (A = Na, K, Rb, NH 4 , and Cs, denoted as Na, K, Rb, NH4, and Cs). Although these fluorogermanophosphates have stoichiometrically equivalent formulas, they feature different anionic clusters, diverse structural dimensionalities, and contrasting crystal symmetries. Chain-like structures were observed for the compounds with the smaller sized alkali ions (Na + , K + , and Rb + ), whereas layered structures were found for those containing the larger sized cations ((NH 4 ) + and Cs + ). Specifically, monoclinic space groups were observed for the Na, K, Rb, and NH4 compounds, whereas a tetragonal space group P4/mbm was found for the Cs compound. These compounds provide new insights into the effects of cation sizes on the anionic clusters built from GeO 4 F 2 octahedra and HPO 4 tetrahedra as well as their influences on the overall structural symmetries in germanophosphates. Further characterization including IR spectroscopy and thermal analyses for all five compounds is also presented.

  14. Activity standardization of 134Cs and 137Cs

    International Nuclear Information System (INIS)

    Sochorová, Jana; Auerbach, Pavel

    2014-01-01

    The paper presents the results from a primary standardization of 137 Cs using two independent methods – efficiency tracing using PC-NaI coincidence and the TDCR method. The nuclides 60 Co and 134 Cs were used as the tracers. Primary standardization of the 134 Cs is also discussed. The efficiency extrapolation was carried out by measuring samples of varying mass and using the wet extrapolation method. The results obtained are in good agreement; the differences did not exceed 0.5%. The advantages, pitfalls and also possibilities for improvement of the procedures are discussed

  15. Influence of the segregation of the granulate from the radwaste-mortar mixture from on the {sup 137}Cs leach-rate; Uticaj segregacije granulata iz sastava betonske - RAO forme na izluzivanje Cs{sup 137}

    Energy Technology Data Exchange (ETDEWEB)

    Peric, A; Plecas, I; Pavlovic, R; Pavlovic, S [Institute of Nuclear Sciences VINCA, Belgrade (Yugoslavia)

    1994-07-01

    In this paper. influence of the segregation of the granulate, presented in the radwaste-mortar matrix formulation, on the {sup 137}Cs, immobilized in the waste form, leach-rate is presented. {sup 137}Cs leach-rates of the two inspected groups of the radwaste-mortar mixture samples were compared, where the first group of the orthocylinder shaped samples was treated due to the Standard Hespe's method and the second group was treated using modified Hespe's method. In the prolonged experimental time, both groups have obtained leach-rate values that are nearly the same, striving to the saturation leach-rate values. This fact indicates that the leaching of the radionuclide as a consequence of the granulate segregation process is in same way rebuilt, as a result of the completed hydratation of the mortar matrix, and 'self healing' of the new open pores and cavities (author)

  16. Introducing a Hydrogen-Bond Donor into a Weakly Nucleophilic Brønsted Base: Alkali Metal Hexamethyldisilazides (MHMDS, M=Li, Na, K, Rb and Cs) with Ammonia.

    Science.gov (United States)

    Neufeld, Roman; Michel, Reent; Herbst-Irmer, Regine; Schöne, Ralf; Stalke, Dietmar

    2016-08-22

    Alkali metal 1,1,1,3,3,3-hexamethyldisilazide (MHMDSs) are one of the most utilised weakly nucleophilic Brønsted bases in synthetic chemistry and especially in natural product synthesis. Like lithium organics, they aggregate depending on the employed donor solvents. Thus, they show different reactivity and selectivity as a function of their aggregation and solvation state. To date, monomeric LiHMDS with monodentate donor bases was only characterised in solution. Since the first preparation of LiHMDS in 1959 by Wannagat and Niederprüm, all efforts to crystallise monomeric LiHMDS in the absence of chelating ligands failed. Herein, we present ammonia adducts of LiHMDS, NaHMDS, KHMDS, RbHMDS and CsHMDS with unprecedented aggregation motifs: 1) The hitherto missing monomeric key compound in the LiHMDS aggregation architectures. Monomeric crystal structures of trisolvated LiHMDS (1) and NaHMDS (2), showing unique intermolecular hydrogen bonds, 2) the unprecedented tetrasolvated KHMDS (3) and RbHMDS (4) dimers and 3) the disolvated CsHMDS (5) dimer with very close intermolecular Si-CH3 ⋅⋅⋅Cs s-block "agostic" interactions have been prepared and characterised by single-crystal X-ray structure analysis. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  17. Comparative study of A-site order in the lead-free bismuth titanates M1/2Bi1/2TiO3 (M=Li, Na, K, Rb, Cs, Ag, Tl) from first-principles

    International Nuclear Information System (INIS)

    Gröting, Melanie; Albe, Karsten

    2014-01-01

    We investigate the possibility of enhancing chemical order in the relaxor ferroelectric Na 1/2 Bi 1/2 TiO 3 upon substitution of Na + by other monovalent cations M + using total energy calculations based on density functional theory. All chemically available monovalent cations M + , which are Li, Na, Ag, K, Tl, Rb and Cs, are considered and an analysis of the structurally relaxed structures in terms of symmetry-adapted distortion modes is given in order to quantify the chemically induced structural distortions. We demonstrate that the replacement of Na + by other monovalent cations can hardly alter the tendency of chemical order with respect to Na 1/2 Bi 1/2 TiO 3 . Only Tl 1/2 Bi 1/2 TiO 3 and Ag 1/2 Bi 1/2 TiO 3 show enhanced tendency for chemical ordering. Both heavy metals behave similar to the light alkali metals in terms of structural relaxations and relative stabilities of the ordered configurations. Although a comparison of the Goldschmidt factors of components (M TiO 3 ) − reveals for Tl a value above the upper stability limit for perovskites, the additional lone-pair effect of Tl + stabilizes the ordered structure. - Graphical abstract: Amplitudes of chemically induced distortion modes in different ordered perovskites M 1/2 Bi 1/2 TiO 3 and visualisation of atomic displacements associated with distortion mode X + 1 in the 001-ordered compounds Li 1/2 Bi 1/2 TiO 3 and Cs 1/2 Bi 1/2 TiO 3 . Due to a substantial size mismatch between bismuth (green) and caesium (dark blue), incorporation of the latter leads to enhanced displacements of oxygen atoms (red) and suppresses displacements of titanium (silver) as compared to lithium (light blue) or other smaller monovalent cations. - Highlights: • Lead-free A-site mixed bismuth titanates M 1/2 Bi 1/2 TiO 3 are studied by first-principles calculations. • Investigation of chemical ordering tendency for M=Li, Na, K, Rb, Cs, Ag, and Tl. • Group theoretical analysis of different ordered structures. • Ag and Tl

  18. Experimental determination of the transfer functions feed/beaf, feed/pork, feed/milk for Cs-137, Co-60, Mu-54, Na-22, I-131, and Tc-95m

    International Nuclear Information System (INIS)

    Voigt, G.; Henrichs, K.; Proehl, G.; Paretzke, H.G.

    1986-05-01

    After the Chernobyl reactor accident, experimental studies have been made with a group of animals, and the results measured are presented in tabular form. The transfer factors of Na-22 have been found to be affected by the daily amount of stable sodium content in the feed. Mn-54 quantities in the feed have been too low to be measured. For two different feeding modes, equilibrium transfer factors of Co and Cs have been determined in pork. As to cereals and potatoe diets, upper limits of transfer have been found. The data obtained for the transfer factor of iodine to milk are in good agreement with published data. (DG) [de

  19. Concentration dependence of the light yield and energy resolution of NaI:Tl and CsI:Tl crystals excited by gamma, soft X-rays and alpha particles

    CERN Document Server

    Trefilova, L N; Kovaleva, L V; Zaslavsky, B G; Zosim, D I; Bondarenko, S K

    2002-01-01

    Based on the analysis of light yield dependence on activator concentration for NaI:Tl and CsI:Tl excited by gamma-rays, soft X-rays and alpha-particles, an explanation of the effect of energy resolution enhancement with the rise of Tl content has been proposed. Based on the concept regarding the electron track structure, we proposed an alternative explanation of the intrinsic resolution value. The concept does not take into account the non-proportional response to electrons of different energies and is based on the statistic fluctuation of scintillation photon number formed outside and inside the regions of higher ionization density.

  20. Radiative transitions for the Cs2NaErCl6 elpasolite crystal. I.- Vibronic intensities for the emissions |(4115/2)Γk]≤| (4I13/2)Γl] in the Cs2NaErCl6

    International Nuclear Information System (INIS)

    Acevedo, R.; Escudero, M; Navarro, G; Meruane, T

    2002-01-01

    In this paper, we report explicit calculations for the spectral intensities of the seventy-five emissions |( 4 I 1372 )Γ k ]→ ( 4 I 15/2 )Γ l ] +v m ; m=3,4,6, where the irreducible representations labels are chosen as: (Γ k ; Γ l )=(Γ 6 ,2Γ 7 ,2Γ 8 ; Γ 6 , Γ 7 ,3Γ 8 , of the ErCl 3- 6 clusters in the Cs 2 NaErCl 6 crystal. The details of the spectrum suggest that in an energy range of about 400cm -1 , a substantial number of transitions [25 magnetic dipole (MD) and 75 vibronic electric dipole (VED) excitations] may be observed and also that a number of super positions of these transitions is most likely to occur. This experimental evidence is rather complicated to analyze and there is a need for more theoretical backup to gain understanding in both radiative and non-radiative processes in these materials. In this paper, we have taken a broader view of the intensity mechanisms associated with vibronically allowed electronic transitions and have decided to further test our current calculation models (VCF-LP) with reference to the |( 4 I 13/2 )Γ k ]→|( 4 I 15/2 )Γl]+v m , emissions for this crystal. It is interesting to realize that, although the intrinsic limitations of our models and methods to estimate spectral intensities, the final output (calculated oscillator strengths) indicate a fair and sensible agreement between our theoretical predictions and experimental data. As a further test of our vibronic intensity model, in a forthcoming paper, we will examine the rather unusual high intensity associated with the |( 4 S 3/ ) Γ l →|( 4 I 15/2 )Γ k ] emissions for this elpasolite (author)

  1. Radiative transitions for the Cs2NaErCl6 elpasolite crystal. II.- Vibronic intensities for the emissions |(4S3/2Γ8]→4I15/2Γ] in the Cs2NaErCl6

    International Nuclear Information System (INIS)

    Acevedo, R.; Escudero, M; Navarro, G; Meruane, T

    2002-01-01

    We have recently reported explicit vibronic intensity calculations for the emissions |( 4 I 15/ ) Γ k ]→|( 4 I 13/2 )Γ l ] of Er 3+ in the Cs 2 NaErCl 6 elpasolite system. The experimental evidence indicates than over an energy range of about 400cm -1 , a substantial number of transitions take place (about one hundred excitations; twenty five of them are magnetic dipole allowed whereas the remaining seventy five are vibronically allowed in character). The spectrum is very complex indeed and the superposition of various spectral features is most likely to occur and this represents a serious challenge to theoreticians. For this system, there is solid evidence which indicates that for the |( 4 S 3/2 )Γ 8 ]→|( 4 I 15/2 )Γ] transitions, where Γ=Γ 6 , Γ 7 , Γ 8 a , Γ 8 b , Γ 8 c , the most intense features of the spectrum are assigned to one photon electric-dipole vibronic excitations, involving the v 3 (stretching; τ 1u ), v 4 (bending; τ 1u ) and v 6 (bending; τ 2u ) moiety modes of the ErCl 3- 6 clusters in the crystal. It is the aim of this paper to explain on both a qualitative and a quantitative basis the rather unexpected high intensity with these type of transitions for which the static selection rule ΔJ=6 is operative. To achieve our goals, we introduce an intensity path and/or mechanism, according to the following radiative decay cascade: |( S 3/2 )Γ 8 ]→|( 4 I 11/2 )Γ']→|( 4 I 15/2 )]. It is shown that when this mechanism is adopted, then the calculated overall spectral intensity due to the three false origins (v 3 , v 4 , v 6 ) is in a fairly good agreement with experiment (author)

  2. A apropriação de imagens de arquivo na obra de Harun Farocki e Péter Forgács

    Directory of Open Access Journals (Sweden)

    Jamer Guterres de Mello

    2012-12-01

    Full Text Available This paper aims to discuss the use of archival and found footage as aprocedure whose objective is to stand out aesthetical and discursive singularities thatmisplace images original senses and create new senses for them. For this purpose, someaspects of the filmography of Harun Farocki and Péter Forgács will be analyzed. These twoartists have been adopting this gesture of appropriation, causing the re-signification of theoriginal meanings of the images.Keywords:

  3. Na, Mg, Ni and Cs distribution and speciation after long-term alteration of a simulated nuclear waste glass: A micro-XAS/XRF/XRD and wet chemical study

    Science.gov (United States)

    Curti, Enzo; Dähn, Rainer; Farges, François; Vespa, Marika

    2009-04-01

    Microscopic distribution and speciation of Na, Mg, Ni and Cs in a simulated (inactive) nuclear waste glass were studied using micro X-ray fluorescence (μ-XRF) and micro X-ray absorption spectroscopy (μ-XAS), after aqueous leaching during 12 years at 90 °C. Na and Mg are major constituents of the glass that can be used to determine the progress of the glass corrosion process and the nature of secondary alteration phases. Ni and Cs represent dose determining long-lived radionuclides ( 59Ni, 135Cs) in vitrified nuclear waste. The Na-Mg μ-XRF maps revealed that the core regions of the glass fragments are apparently unaltered and compositionally homogeneous, whereas rims and interstitial spaces are enriched with Mg-rich smectite formed during the leaching process. The micro X-ray absorption near edge structure (μ-XANES) spectra collected at the Mg K-edge in the altered zones show three sharp resonances typical for crystalline Mg-silicates. These resonances are distinctive of Mg occupying undistorted octahedral positions. In contrast, the μ-XANES spectra collected in the core zones of the glass fragments lack this resonance pattern and are identical to the spectra measured on the pristine (unleached) MW glass. Micro extended X-ray absorption fine structure (μ-EXAFS) and μ-XANES analyses at the Ni K-edge revealed three distinct Ni(II) species: (a) Ni uniformly distributed in the glass matrix, (b) micro-inclusions with high Ni concentrations and (c) Ni associated to the Mg-clay. The comparison with reference spectra of unleached MW and other Ni-bearing silicate glasses indicated that species (a) represents the original coordinative environment of Ni in the glass. The μ-EXAFS analyses revealed that species (b) is structural Ni in trevorite (NiFe 2O 4), which probably formed through unmixing processes during the cooling of the glass melt. The μ-EXAFS of species (c) could be successfully modeled assuming specific adsorption or incorporation of Ni into the lattice of

  4. Radiocesium bioaccumulation in freshwater plankton: Influences of cation concentrations (K{sup +} and Na{sup +}) on direct uptake of {sup 137}Cs in Chlamydomonas, Scenedesmus and Daphnia. Food-chain transfer of {sup 137}Cs from Chlamydomonas to Daphnia at different K{sup +} concentrations

    Energy Technology Data Exchange (ETDEWEB)

    Hagstroem, J. [Uppsala Univ., Dept. of Limnology, Uppsala (Sweden)

    2002-04-01

    The influences of cation concentrations (K{sup +} and Na{sup +}) on radiocesium ({sup 137}Cs) bioaccumulation in two freshwater phytoplankton species (Scenedesmus quadricauda and Chlamydomonas noctigama) were systematically investigated in batch-cultures monitored during two weeks. Both species were cultured at 9 {mu}E M{sup -2} s{sup -1} constant illumination at 20 deg. C. The exponential growth phase lasted for more than 100 hours ({mu} {approx_equal} 0.02 h{sup -1} for C. noctigama and 0.03 h{sup -1} for S, quadricauda). Over cation concentration ranges encountered in natural fresh waters ([K{sup +}] from 0.1 {mu}M to 3 mM, [Na{sup +}] from 20 {mu}M to 3 mM), a more than three order of magnitude variation was found for both intake rate and observed bioconcentration factors (BCF) at apparent steady-state (from less than 10{sup 3} to 10{sup 6} L (kg C){sup -1}). For both species, the major effector on BCF and uptake rate was external [K{sup +}], which was inversely proportional to these parameters over wide ranges (1-1000 {mu}M for S. quadricauda and 0.1 to 300 {mu}M for C. noctigama). At concentrations above these ranges K{sup +} still reduced {sup 137} Cs bio-uptake, but less effectively. A minor influence of external [Na{sup +}] on {sup 137}Cs bioaccumulation was indicated for S. quadricauda, whereas no such influence was significant for C. noctigama. A biphasic pattern for {sup 137}Cs bioaccumulation was discovered in C. noctigama. A rapid 'quasi-steady state' with an effective equilibration time of less than 100 hours was approached during the exponential growth phase. A surge in the uptake occurred when exponential growth ceased, and this pattern was consistent over the range 30 {mu}M to 1.4 mM external [K{sup +}]. Since depletion of external [K{sup +}] was not detected for these treatments, this pattern can only be explained if there are at least two different cellular compartments involved. Although less certain, a second steady-state BCF

  5. Variable dimensionality and framework found in a series of quaternary zinc selenites, A{sub 2}Zn{sub 3}(SeO{sub 3}){sub 4}·xH{sub 2}O (A = Na, Rb, and Cs; 0≤x≤1) and Cs{sub 2}Zn{sub 2}(SeO{sub 3}){sub 3}·2H{sub 2}O

    Energy Technology Data Exchange (ETDEWEB)

    Lü, Minfeng; Jo, Hongil; Oh, Seung-Jin; Ok, Kang Min, E-mail: kmok@cau.ac.kr

    2017-01-15

    Five new alkali metal zinc selenites, A{sub 2}Zn{sub 3}(SeO{sub 3}){sub 4}·xH{sub 2}O (A = Na, Rb, and Cs; 0≤x≤1) and Cs{sub 2}Zn{sub 2}(SeO{sub 3}){sub 3}·2H{sub 2}O have been synthesized by heating a mixture of ZnO, SeO{sub 2} and A{sub 2}CO{sub 3} (A = Na, Rb, and Cs), and characterized by X-ray diffraction (XRD) and spectroscopic analyses techniques. All of the reported materials revealed a rich structural chemistry with different frameworks and connection modes of Zn{sup 2+}. While Rb{sub 2}Zn{sub 3}(SeO{sub 3}){sub 4} and Cs{sub 2}Zn{sub 3}(SeO{sub 3}){sub 4}·H{sub 2}O revealed three-dimensional frameworks consisting of isolated ZnO{sub 4} tetrahedra and SeO{sub 3} polyhedra, Na{sub 2}Zn{sub 3}(SeO{sub 3}){sub 4}, Cs{sub 2}Zn{sub 3}(SeO{sub 3}){sub 4}, and Cs{sub 2}Zn{sub 2}(SeO{sub 3}){sub 3}·2H{sub 2}O contained two-dimensional [Zn{sub 3}(SeO{sub 3}){sub 4}]{sup 2-} layers. Specifically, whereas isolated ZnO{sub 4} tetrahedra and SeO{sub 3} polyhedra are arranged into two-dimensional [Zn{sub 3}(SeO{sub 3}){sub 4}]{sup 2-} layers in two cesium compounds, circular [Zn{sub 3}O{sub 10}]{sup 14-} chains and SeO{sub 3} linkers are formed in two-dimensional [Zn{sub 3}(SeO{sub 3}){sub 4}]{sup 2-} layers in Na{sub 2}Zn{sub 3}(SeO{sub 3}){sub 4}. Close structural examinations suggest that the size of alkali metal is significant in determining the framework geometry as well as connection modes of transition metal cations. - Graphical abstract: Variable dimensions and frameworks were found in a series of quaternary zinc selenites, A{sub 2}Zn{sub 3}(SeO{sub 3}){sub 4} (A = Na, Rb and Cs). - Highlights: • Five novel quaternary zinc selenites are synthesized. • All the selenites with different structures contain polarizable d{sup 10} and lone pair cations. • The size of alkali metal cations is significant in determining the framework geometry.

  6. Photocrystallography at TriCS/SINQ: light-induced structural changes in Na2[Fe(CN)5NO]2H2O

    International Nuclear Information System (INIS)

    Schefer, J.; Schaniel, D.; Woike, Th.; Imlau, M.

    2004-01-01

    Light-induced metastable electronic states as observed e.g. in sodium nitroprusside are of fundamental interest for data storage and optical computing. Structural functionality and therefore the light-induced structure itself is of basic interest in such systems. As neutrons are sensitive to the position of the nucleus and non-destructive with respect to the metastable electronic states, neutron photocrystallography provides a useful method to determine light-induced structural changes. A photocrystallographic experimental setup has been built-up at SINQ and has been successfully used at the single-crystal instrument TriCS and the test facility TOPSI (now called MORPHEUS)

  7. Report on Three IAEA Intercomparisons: 1) Determination of Potassium and Cs-137 in Animal Blood Serum (A-1); 2) Determination of Sr-90 and Ra-226 in Animal Bone Ash (A-3); 3) Determination of Sr-90, Cs-137, Na, K, Cs, Ca, Sr and Ba in Milk Powder (A-7)

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1973-12-01

    The samples were made from fresh animal blood by separating the blood particles from the serum, stirring and subsequent spray drying. No spiking with active or inactive materials was made. Each participating laboratory received a 500 g sub-sample of the material. In the case of {sup 137}Cs-analysis, two of the laboratories submitted two different sets of results which were obtained by different analytical methods. Results were presented in separate tables for both elements.

  8. Adsorption of Cs+, Ni2+ and lanthanides onto a kaolinite and Na-montmorillonite up to 1500C: an experimental and modeling study

    International Nuclear Information System (INIS)

    Tertre, E.

    2005-10-01

    The motivation for this study is to assess the temperature effect on the clay minerals sorption properties. Sorption and desorption of Cs + , Ni 2+ et Ln 3+ onto a montmorillonite and a kaolinite were performed by batch experiments between 25 and 150 C, and in different pH and ionic strengths conditions. Sorption enthalpies varying between 0 and 80 kJ/mol were then calculated. For europium, surface spectroscopic analyses confirmed that the mechanism involved is adsorption, including at 150 C. Moreover, this method allowed us to obtain qualitatively the different adsorption equilibrium occurring during the reaction. An acid/base study of the clay surfaces was performed in order to assess the temperature effect on the surface charge of these minerals. Then, a surface complexation model including edge sites and structural sites was proposed to interpret the acid/base data and the europium sorption data. (author)

  9. A Novel Ruthenium-Decorating Polyoxomolybdate Cs3Na6H[MoVI14RuIV2O50(OH2]·24H2O: An Active Heterogeneous Oxidation Catalyst for Alcohols

    Directory of Open Access Journals (Sweden)

    Rong Wan

    2018-01-01

    Full Text Available The first example of wholly inorganic ruthenium-containing polyoxomolybdate Cs3Na6H[MoVI14RuIV2O50(OH2]·24H2O (1 was isolated and systematically characterized by element analysis, infrared spectroscopy (IR, thermogravimetric analyses (TGA, X-ray photoelectron spectroscopy (XPS, energy dispersive X-ray spectroscopy (EDX and single-crystal X-ray diffraction. Compound 1 is composed of an unprecedented {Mo14}-type isopolymolybdate with a di-ruthenium core precisely encapsulated in its center, exhibiting a three-tiered ladder-like structure. The title compound can act as an efficient heterogeneous catalyst in the transformation of 1-phenylethanol to acetophenone. This catalyst is also capable of being recycled and reused for at least ten cycles with its activity being retained under the optimal conditions.

  10. Chemical trends of the band gaps of idealized crystal of semiconducting silicon clathrates, M8Si38A8 (M = Na, K, Rb, Cs; A = Ga, Al, In), predicted by first-principle pseudopotential calculations

    International Nuclear Information System (INIS)

    Imai, Yoji; Imai, Motoharu

    2011-01-01

    Research highlights: → This paper reports the results of electronic structural calculations of Si clathrate, M 8 Si 38 Ga 8 (M: the encapsulated guest alkali atom; Na, K, Rb, and Cs). → All of them are found to be indirect semiconductors with the calculated gaps (E g ) from 0.45 to 0.89 eV, which should be compared to the calculated gap of 0.65 eV of crystalline Si with the diamond structure. The gaps become wider with the promotion to the heavier guest alkali atoms and the reasons of gap widening are discussed using the calculated dependence of E g on the cell-volume of guest-free silicon clathrate (Si 46 ). Effect of the substitutional elements in the clathrate framework (Al and In in place of Ga) was also discussed. - Abstract: We have calculated the band structures of Si clathrate, M 8 Si 38 Ga 8 (M = Na, K, Rb, and Cs), using the density-functional theory under the generalized gradient corrected local density approximation, where M is the encapsulated guest alkali atom. They are found to be indirect semiconductors with the calculated gaps (E g ) from 0.45 to 0.89 eV, which should be compared to the calculated gap of 0.65 eV of crystalline Si with the diamond structure. The gaps become wider with the promotion to the heavier guest alkali atoms and the reasons of gap widening are discussed using the calculated dependence of E g on the cell-volume of guest-free silicon clathrate (Si 46 ). Effect of the substitutional elements in the clathrate framework (Al and In in place of Ga) was also discussed.

  11. CS Informativeness Governs CS-US Associability

    Science.gov (United States)

    Ward, Ryan D.; Gallistel, C. R.; Jensen, Greg; Richards, Vanessa L.; Fairhurst, Stephen; Balsam, Peter D

    2012-01-01

    In a conditioning protocol, the onset of the conditioned stimulus (CS) provides information about when to expect reinforcement (the US). There are two sources of information from the CS in a delay conditioning paradigm in which the CS-US interval is fixed. The first depends on the informativeness, the degree to which CS onset reduces the average expected time to onset of the next US. The second depends only on how precisely a subject can represent a fixed-duration interval (the temporal Weber fraction). In three experiments with mice, we tested the differential impact of these two sources of information on rate of acquisition of conditioned responding (CS-US associability). In Experiment 1, we show that associability (the inverse of trials to acquisition) increases in proportion to informativeness. In Experiment 2, we show that fixing the duration of the US-US interval or the CS-US interval or both has no effect on associability. In Experiment 3, we equated the increase in information produced by varying the C̅/T̅ ratio with the increase produced by fixing the duration of the CS-US interval. Associability increased with increased informativeness, but, as in Experiment 2, fixing the CS-US duration had no effect on associability. These results are consistent with the view that CS-US associability depends on the increased rate of reward signaled by CS onset. The results also provide further evidence that conditioned responding is temporally controlled when it emerges. PMID:22468633

  12. Cs2UPd3Se6

    Directory of Open Access Journals (Sweden)

    George N. Oh

    2011-02-01

    Full Text Available Dicaesium uranium(IV tripalladium(II hexaselenide, Cs2UPd3Se6, crystallizes in the space group Fmmm in the Ba2NaCu3O6 structure type. The asymmetric unit comprises the following atoms with site symmetries as shown: U1 (mm2, Cs1 (222, Cs2 (m2m, Pd1 (.m., Pd2 (2mm, Se1 (m.., and Se2 (1. This layered structure contains six edge-sharing square-planar [PdSe4] units that form a hexagon. These, in turn, edge-share with [USe6] trigonal–prismatic units, forming an extended layer parallel to (010. The layers are stacked along [010]. They are staggered, and are separated by the Cs atoms. The Cs atoms are either coordinated in a square antiprism of Se atoms or are ten-coordinate, with one square face and the opposite face hexagonal.

  13. Applicability of a portable CdTe and NaI (Tl) spectrometer for activity measure; Aplicabilidade de um espectrometro portatil de CdTe e NaI (Tl) para a medida da atividade de Cesio-137 ({sup 137}Cs) e Berilio-7 ({sup 7}Be)

    Energy Technology Data Exchange (ETDEWEB)

    Fernandes, Jaquiel Salvi

    2005-02-15

    In this work it was studied the application of an in situ gamma spectrometer (ROVER) of Amptek Inc., composed by a Cadmium Telluride detector (CdTe) of 3 mm x 3 mm x 1 mm and a 30 mm x 30 mm Sodium Iodide detector doped with Thallium [NaI (Tl)). The radioactive sources used were type pastille, sealed in aluminum and polyethylene, of {sup 241}Am, {sup 133}Ba, {sup 152}Eu, 3 sources of {sup 137}Cs and soil samples contaminated with {sup 137}Cs. It was performed a factorial planning 2{sup 3} to optimize the in situ spectrometry system. This way it was determined that the best temperature for CdTe crystal operation is -22, deg C, with Shaping Time of 3 {mu}S and Rise Time Discrimination (RTD) with value 3. With the help of the certified radioactive sources, we determined the efficiency curve of the two detectors. The CdTe detector was positioned at the standard distance of 1 meter of the sources and also at 4.15 cm. The NaI (Tl) detector was also positioned at the standard distance of 1 meter of the sources and at 2.8 cm. Measures were performed to determine the Minimum Detectable Activity (MDA) for both detectors. For the pastille type sources, the {sup 137}Cs MDA for the CdTe detector at 4.15 cm, analyzing the energy line of 32 keV, was 6 kBq and at 1 meter of the {sup 137}Cs source, analyzing the line of 661.65 keV, the MDA was 67 kBq. For soil samples, CdTe detector at 4.15 cm presented a MDA of 693 kBq.kg-l for the line of 32 keV, and for the soil sample {sup 7}Be content the MDA found was 2867 Bq.kg{sup -1} at 4.15 cm. For the NaI (Tl) detector, analyzing the line of 661.65 keV, the {sup 137}Cs MDA for pastille type source at 1 meter of distance was 7 kBq, and for soil sample at 2.8 cm the measured {sup 137}Cs MDA was 71 Bq.kg{sup -1}. For the soil sample {sup 7}Be content, at 2.8 cm of the Nal (Tl) detector, the obtained MDA was 91 Bq.kg{sup -1}. Due to the minimum detectable activities found for the two detectors, we concluded that the employed in situ gamma

  14. Inorganic alkali lead iodide semiconducting APbI3 (A = Li, Na, K, Cs and NH4PbI3 films prepared from solution: Structure, morphology, and electronic structure

    Directory of Open Access Journals (Sweden)

    Eric Mankel

    2016-06-01

    Full Text Available APbI3 alkali lead iodides were prepared from aqueous (A= Na, Cs, ammonium NH4+, and methyl­ammonium CH3NH3+ and acetone (A= Li, K solutions by a self-organization low temperature process. Diffraction analysis revealed that the methylammonium-containing system (MAPbI3 crystallizes into a tetragonal perovskite structure, whereas the alkali and NH4+ systems adopt orthorhombic structures. Morphological inspection confirmed the influence of the cation on the growth mechanism: for A = Cs and NH4+, needle-like crystallites with lengths up to 3–4 mm; for A = K, thin stripes with lengths up to 5–6 mm; and for A = MA+, dodecahedral crystallites were observed. For A = Li and Na, the APbI3 systems typically resulted in polycrystalline aggregates. Optical absorption measurements demonstrated large energy band gaps for the alkali and ammonium systems with values between 2.19 and 2.40 eV. For electronic and chemical characterization by photoelectron spectroscopy, the as-prepared powders were dissolved in di-methylformamide and re-crystallized as thin films on F:SnO2 substrates by spin-coating. The binding energy differences between Pb4f and I3d core levels are highly similar in the investigated systems and close to the value measured for PbI2, indicating similar relative partial charges and formal oxidation states. The binding energies of the alkali ions are in accordance with oxidation state +1. The X-ray excited valence band spectra of the investigated APbI3 systems exhibited similar line shapes in the region between the valence band maximum and 4.5 eV higher binding energy due to common PbI6 octahedra which dominate the electronic structure. While the ionization energy values are quite similar (6.15 ± 0.25 eV, the Fermi-level positions of the unintentionally doped materials vary for different cations and different batches of the same material, which indicates that the position of the Fermi level can be influenced by changing the process parameters.

  15. Gadolinium released by the linear gadolinium-based contrast-agent Gd-DTPA decreases the activity of human epithelial Na+ channels (ENaCs).

    Science.gov (United States)

    Knoepp, Fenja; Bettmer, Joerg; Fronius, Martin

    2017-05-01

    Gadolinium-based-contrast-agents (GBCAs) are used for magnetic-resonance-imaging and associated with renal and cardiovascular adverse reactions caused by released Gd 3+ ions. Gd 3+ is also a modulator of mechano-gated ion channels, including the epithelial Na + channel (ENaC) that is expressed in kidney epithelium and the vasculature. ENaC is important for salt-/water homeostasis and blood pressure regulation and a likely target of released Gd 3+ from GBCAs causing the above-mentioned adverse reactions. Therefore this study examined the effect of Gd 3+ and GBCAs on ENaC's activity. Human αβγENaC was expressed in Xenopus laevis oocytes and exposed to Gd 3+ , linear (Gd-DTPA, Magnevist) or cyclic (Dotarem) GBCAs. Transmembrane ion-currents (I M ) were recorded by the two-electrode-voltage-clamp technique and Gd 3+ -release by Gd-DTPA was confirmed by inductively coupled plasma-mass spectrometry. Gd 3+ exerts biphasic effects on ENaC's activity: ≤0.3mmol/l decreased I M which was preventable by DEPC (modifies histidines). Strikingly Gd 3+ ≥0.4mmol/l increased I M and this effect was prevented by cysteine-modifying MTSEA. Linear Gd-DTPA and Magnevist mimicked the effect of ≤0.3mmol/l Gd 3+ , whereas the chelator DTPA showed no effect. Gd 3+ and Gd-DTPA increased the IC 50 for amiloride, but did not affect ENaC's self-inhibition. Interestingly, cyclic Gd-DOTA (Dotarem) increased I M to a similar extent as its chelator DOTA, suggesting that the chelator rather than released Gd 3+ is responsible for this effect. These results confirm Gd 3+ -release from linear Gd-DTPA and indicate that the released Gd 3+ amount is sufficient to interfere with ENaC's activity to provide putative explanations for GBCA-related adverse effects. Copyright © 2017 Elsevier B.V. All rights reserved.

  16. Optical spectroscopy of Cm{sup 3+} in the elpasolite Cs{sub 2} NaYCl{sub 6}. Application in the structural study of Cm(III) sorption on phosphate materials; Spectroscopie optique de Cm{sup 3+} dans l`elpasolite Cs{sub 2}NaYCl{sub 6}. Application a l`etude structurale de la sorption de Cm(III) sur des materiaux phosphates

    Energy Technology Data Exchange (ETDEWEB)

    Cavellec, Ronan [Universite de Paris Sud, 91 - Orsay (France)

    1998-05-15

    Radwaste management involves important research. In order to contribute to this program we proposed the examination of two different and complementary aspects of nuclear waste: the detection by laser spectroscopy of trivalent actinide ions diluted in a crystal host and the migration of radionuclides through different barriers in geosphere that is related to understanding and modelling the sorption processes. In both cases the spectro-fluorimetry laser is used to investigate different phenomenological processes at microscopic scale. The first part of the thesis deals with the investigation of Cm{sup 3+} energy levels in Cs{sub 2}NaYCl{sub 6}. From the analysis of excitation and emission spectra 52 crystal-field levels have been assigned and the phenomenological parameters calculated. A discussion about these parameters, compared with those in case of LaCl{sub 3} and ThO{sub 2} cases, is given. An intense green fluorescence has been found for the first time for Cm{sup 3+} in elpasolite. Thus, this material seems to be a promising solid for the analytical application of actinides such as Cm{sup 3+} and Am{sup 3+} ions. In the second part the sorption of curium (5{center_dot}10{sup -8} mol {center_dot}l{sup -1}) onto phosphate materials was studied. The ionic strength, electrolyte nature and complexing agent were investigated. The laser spectro-fluorimetry is shown to be a powerful technique. The formation of surface complexes for ZrP{sub 2}O{sub 7}, Zr{sub 2}O(PO{sub 4}){sub 2} and Th{sub 4}(PO{sub 4}){sub 4}P{sub 2}O{sub 7} has been demonstrated. Fluorescence lifetime measurements indicate that in complexing medium the aqueous complex of Cm is sorbed preferentially to the Cm{sup 3+} free ion onto the solid 82 refs., 54 figs., 35 tabs.

  17. Hydrothermal synthesis and crystal structures of Na{sub 2}Be{sub 3}(SeO{sub 3}){sub 4}.H{sub 2}O and Cs{sub 2}[Mg(H{sub 2}O){sub 6}]{sub 3}(SeO{sub 3}){sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Shen, Chen; Mei, Dajiang; Sun, Chuanling; Liu, Yunsheng; Wu, Yuandong [College of Chemistry and Chemical Engineering, Shanghai University of Engineering Science (China)

    2017-09-04

    The selenites, Na{sub 2}Be{sub 3}(SeO{sub 3}){sub 4}.H{sub 2}O and Cs{sub 2}[Mg(H{sub 2}O){sub 6}]{sub 3}(SeO{sub 3}){sub 4}, were synthesized under hydrothermal conditions. The crystal structures of Na{sub 2}Be{sub 3}(SeO{sub 3}){sub 4}.H{sub 2}O and Cs{sub 2}[Mg(H{sub 2}O){sub 6}]{sub 3}(SeO{sub 3}){sub 4} were determined by single-crystal X-ray diffractions. Na{sub 2}Be{sub 3}(SeO{sub 3}){sub 4}.H{sub 2}O crystallizes in the triclinic space group P1 (no. 2) with unit cell parameters a = 4.8493(9), b = 12.013(2), c = 12.077(2) Aa, and Z = 2, whereas Cs{sub 2}[Mg(H{sub 2}O){sub 6}]{sub 3}(SeO{sub 3}){sub 4} crystallizes in the monoclinic space group C2/m (no. 12) with lattice cell parameters a = 12.596(6), b = 7.297(4), c = 16.914(8) Aa, and Z = 2. Na{sub 2}Be{sub 3}(SeO{sub 3}){sub 4}.H{sub 2}O features a three-dimensional open framework structure formed by BeO{sub 4} tetrahedra and SeO{sub 3} trigonal pyramids. Na cations and H{sub 2}O molecules are located in different tunnels. Cs{sub 2}[Mg(H{sub 2}O){sub 6}]{sub 3}(SeO{sub 3}){sub 4} has a structure composed of isolated [Mg(H{sub 2}O){sub 6}] octahedra and SeO{sub 3} trigonal pyramids interacted by hydrogen bonds, and Cs cations are resided in-between. Both compounds were characterized by thermogravimetric analysis and FT-IR spectroscopy. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  18. Improving CS regulations.

    Energy Technology Data Exchange (ETDEWEB)

    Nesse, R.J.; Scheer, R.M.; Marasco, A.L.; Furey, R.

    1980-10-01

    President Carter issued Executive Order 12044 (3/28/78) that required all Federal agencies to distinguish between significant and insignificant regulations, and to determine whether a regulation will result in major impacts. This study gathered information on the impact of the order and the guidelines on the Office of Conservation and Solar Energy (CS) regulatory practices, investigated problems encountered by the CS staff when implementing the order and guidelines, and recommended solutions to resolve these problems. Major tasks accomplished and discussed are: (1) legislation, Executive Orders, and DOE Memoranda concerning Federal administrative procedures relevant to the development and analysis of regulations within CS reviewed; (2) relevant DOE Orders and Memoranda analyzed and key DOE and CS staff interviewed in order to accurately describe the current CS regulatory process; (3) DOE staff from the Office of the General Counsel, the Office of Policy and Evaluation, the Office of the Environment, and the Office of the Secretary interviewed to explore issues and problems encountered with current CS regulatory practices; (4) the regulatory processes at five other Federal agencies reviewed in order to see how other agencies have approached the regulatory process, dealt with specific regulatory problems, and responded to the Executive Order; and (5) based on the results of the preceding four tasks, recommendations for potential solutions to the CS regulatory problems developed. (MCW)

  19. Quantitative Cs-137 distributions from airborne gamma ray data

    International Nuclear Information System (INIS)

    Oberlercher, G.; Seiberl, W.

    1997-01-01

    The Chernobyl reactor accident caused in Austria Cs-137 activities up to 180 kBq/m 2 . The following paper explains how airborne NaJ-spectroscopy, originally designed for geological surveys, was used as an accurate method to obtain the ground activity of Cs-137 in certain regions of Austria. To retrieve the net count rate in a Cs-137 window it is necessary to subtract all background contributions from the peak, including the Compton continuum and the contribution of overlapping peaks. Therefore the measurement of Cs-137 with a NaJ detector system must take into account radioactive elements with gamma-ray lines near the peak energy of Cs-137 at 662 keV. In regions with higher concentrations of the natural radioactive elements uranium and thorium a peak near 600 keV is found, containing the 609 keV line of Bi-214 and the 585 keV line of TI-208. Additionally a Cs-134 line is located at 604 keV. Because of the poor energy resolution of NaJ detectors it is not possible to find a clear separation between these peaks and the Cs-137 peak. The following section describes the method that was used to obtain accurate quantified Cs-137 activity values. (author)

  20. Study of Cs recovery by extraction chromatography (2)

    International Nuclear Information System (INIS)

    Hoshi, Harutaka; Zhang, Anyun; Uchida, Hiromi; Kuraoka, Etsushu

    2005-02-01

    In order to apply CalixR14 extractant to extraction chromatography for Cs separation, basic characteristics of CalixR14 adsorbent were studied. CalixR14 impregnated resin and CalixR14 + TBP impregnated resin were prepared. CalixR14 extractant showed no adsorption for Cs by liquid-liquid extraction and CalixR14 impregnated resin also showed no adsorption for Cs. Therefore, it is concluded that CalixR14 itself has no affinity for Cs. On the other hand, Cs was adsorbed onto CalixR14-TBP impregnated resin from a concentrated nitric acid solution. The distribution coefficients of Cs were more than 10 cm 3 /g from 2 to 6 M nitric acid. While Rb showed week adsorption, Na, K, Sr and La showed no adsorption and separation factor was over 100. A slight amount of CalixR14 and TBP was leaked from impregnated resin into the aqueous phase. Separation from simulated liquid waste was carried out by using a column packed with CalixR14-TBP adsorbent. Na, K, Sr and La were not adsorbed onto the column, however, Cs and Rb were adsorbed onto the column. Cs and Rb were eluted from the column by water. Cs and Rb were quantitatively recovered. (author)

  1. CS Bond formation by

    Indian Academy of Sciences (India)

    2017-02-02

    Feb 2, 2017 ... a thiol substituent at position-2 of the quinazoline ring. ... coupling reactions represent great contribution to the recent growth of organic synthesis.2 ... Difficulties in C-S ...... Experimental Advances (Amsterdam: Elsevier) 19; (b).

  2. Differential leaching of 137Cs from sediment core depth fractions of Bombay harbour bay

    International Nuclear Information System (INIS)

    Hemalatha, P.; Desai, M.V.M.

    1998-01-01

    Bombay harbour bay receives 137 Cs from the effluents of research reactors, fuel reprocessing plant and isotope laboratories. 137 Cs is strongly taken up by suspended particulates and sediments and is trapped in the layer lattices of the clay minerals. As the siltation rate is high in the bay, 137 Cs gets distributed vertically along the depth of sediment. NaCl solution has been proved to desorb 137 Cs from clay minerals effectively. NaCl solution of ionic strength 1.6 was used to desorb 137 Cs from depth fractions of a sediment core to obtain a possible gradient of leaching with the depth. A definite rate of leaching was observed for the 137 Cs in the core sediment depth fractions. About 13% to 56% of 137 Cs was leached. As the depth increases removal rate of cesium decreases. This is expected to bring out a relation between age of 137 Cs and rate of its leaching. (author)

  3. The influence of organic compound addition on the mobility and biological availability of the {sup 137} Cs and {sup 60} Co on tropical soils; A influencia da adicao de composto organico na mobilidade e biodisponibilidade do {sup 137} Cs e do {sup 60} Co em solos tropicais

    Energy Technology Data Exchange (ETDEWEB)

    Portilho, Antonio Passos

    2005-07-01

    The hole of manure in the mobility and bioavailability of {sup 137}Cs and {sup 60}Co in Brazilian soil was investigated. For this study an Oxisol was selected, for being the soil of larger distribution in the country, characterized by a low content in nutrients and organic substances; a Nitisol, was also selected as representative of soils with average fertility and an Organo sol, as representative of soils with high content of organic matter. These soils were transferred to an experimental area in the Instituto de Radioprotecao e Dosimetria, conditioned in plastic pots and spiked with {sup 137}Cs e {sup 60}Co. To follow the root uptake of {sup 137}Cs and {sup 60}Co we cultivated radish (Raphanus sativus, L.), in the pots receiving different doses of manure: a dose recommended for radish (2 kg/m{sup 2}); a half of the recommended dose; the double of the recommended dose and without manure addition. Only the Organo sol did not received manure. Moreover, it was investigated the potential mobility of {sup 137}Cs and {sup 60}Co associated to the unstable compounds under natural soil environment, such as the organic substance, oxides of iron etc, through the method of sequential chemical extraction. The main results show that soil to plant transfer factor (TF) for {sup 137}Cs decreases after the addition of 4 kg/m{sup 2} of manure in the Nitisol (from 0.44 to 0.06) and in the Oxisol (from 0,44 to 0,11). In relation to {sup 60}Co the TF reduced from 14,73 for 0,15 in Nitisol and from 11,25 for 0,15 to Oxisol. In the Organosols the TF values were low and comparable with values obtained in soil that received at least a dose of manure: 0,11 for {sup 137}Cs and 2,64 for {sup 60}Co. It was also observed, that the TF for {sup 137}Cs diminish with the increase of the nutrient contents (K, Ca and Mg) when manure is applied. It was verified, through the results of sequential extraction, that {sup 137}Cs was mainly associated to iron oxides in all types of studied soils. In the

  4. Retention of Cs on zeolite, bentonite and their mixtures

    International Nuclear Information System (INIS)

    Atun, G.

    2002-01-01

    The sorption behavior of cesium on zeolite and bentonite minerals and their mixtures was studied by means of a batch method and a tracer technique. All experiments were carried out in the presence of CsCl spiked with 137 Cs and NaCl as a supporting electrolyte in varying concentrations. The distribution coefficients (K D ) did not show significant differences at low Cs + loadings while they decreased in the high loading region. Freundlich and D-R isotherms were applied to the adsorption data of zeolite and bentonite. Adsorption capacities and mean energies calculated from D-R isotherm parameters decreased by increasing ionic strength on both minerals. The identification of the specific uptake sites was attempted on the basis of the Freundlich isotherm. Experimentally observed distribution coefficients of Cs on two mineral mixtures were smaller than theoretically calculated values, except at the highest NaCl concentration. (author)

  5. Study of {sup 137} Cs contamination in Rochedo Reservoir, Meia Ponte river (Goias State) from the radiologic accident in Goiania; Estudo da contaminacao por {sup 137} Cs na Represa do Rochedo, Rio Meia Ponte (GO), proveniente do acidente radiologico de Goiania

    Energy Technology Data Exchange (ETDEWEB)

    De Luca, Marcia Emilia M. [Universidade Federal, Rio de Janeiro, RJ (Brazil). Inst. de Biofisica; Godoy, Jose Marcos O. [Instituto de Radioprotecao e Dosimetria (IRD), Rio de Janeiro, RJ (Brazil)

    1997-12-31

    Through {sup 137} Cs concentration profiles in sediments from Rochedo Reservoir, it was possible to estimate the amount of this radionuclide (94 GBq) which has reached the Meia Ponte River system, as a consequence of the Goiania radiological accident in 1987. Based on in-situ measurements as well as on laboratory studies, the influence of N H{sub 4}{sup +} concentration on the K{sub d} value was also investigated. The results have shown that for high N H{sub 4}{sup +} concentrations there is a clear correlation between both parameters. It was also observed the influence on the aging effect on the {sup 137} Cs release from the sediment, as well as of the illite content in it. (author) 9 refs., 6 figs.

  6. Comparison among the rice bark in the raw and active forms in the removal of {sup 241}Am and {sup 137}Cs from liquid radioactive wastes; Comparacao entre a casca de arroz nas formas brutas e ativada na remocao de {sup 241}Am e {sup 137}Cs de rejeitos radioativos liquidos

    Energy Technology Data Exchange (ETDEWEB)

    Ferreira, Rafael V.P.; Lima, Josenilson B. de; Bellini, Maria Helena; Sakata, Solange Kazumi; Marumo, Julio Takehiro, E-mail: rpadua@ipen.b, E-mail: sksakata@ipen.b, E-mail: jblima@ipen.b, E-mail: mbmarumo@ipen.b, E-mail: jtmarumo@ipen.b [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2011-10-26

    New techniques involving treatment of radioactive wastes which associate simplicity and low cost have been directed the attention for the bio sorption, which is a process were solid vegetable or micro-organism for the retention, removing, or recovering of heavy metals from a liquid environment. This study evaluated the capacity of a bio sorbent to remove Am-241 and Cs-137 from liquid radioactive waste. The chosen material was the rice bark employed in the raw or activated forms. The obtained results suggest that the bio sorption, with the activated rice bark, can be a viable technique for the treatment of liquid radioactive wastes containing Am-241 and Cs-137 present in liquid radioactive wastes

  7. Geant4 simulations of the absorption of photons in CsI and NaI produced by electrons with energies up to 4 MeV and their application to precision measurements of the β-energy spectrum with a calorimetric technique

    Science.gov (United States)

    Huyan, X.; Naviliat-Cuncic, O.; Voytas, P.; Chandavar, S.; Hughes, M.; Minamisono, K.; Paulauskas, S. V.

    2018-01-01

    The yield of photons produced by electrons slowing down in CsI and NaI was studied with four electromagnetic physics constructors included in the Geant4 toolkit. The subsequent absorption of photons in detector geometries used for measurements of the β spectrum shape was also studied with a focus on the determination of the absorption fraction. For electrons with energies in the range 0.5-4 MeV, the relative photon yields determined with the four Geant4 constructors differ at the level of 10-2 in amplitude and the relative absorption fractions differ at the level of 10-4 in amplitude. The differences among constructors enabled the estimation of the sensitivity to Geant4 simulations for the measurement of the β energy spectrum shape in 6He decay using a calorimetric technique with ions implanted in the active volume of detectors. The size of the effect associated with photons escaping the detectors was quantified in terms of a slope which, on average, is respectively - 5 . 4 %/MeV and - 4 . 8 %/MeV for the CsI and NaI geometries. The corresponding relative uncertainties as determined from the spread of results obtained with the four Geant4 constructors are 0.0067 and 0.0058.

  8. Thermal Vibrations of Beta-Brass and the Order-Disorder Transition; Vibrations Thermiques dans le Laiton Beta et Transformation Ordre-Desordre; Teplovye kolebaniya beta-latuni i perekhod iz uporyadochennogo sostoyaniya v razuporyadochennoe; Vibraciones Termicas del Laton Beta y Transicion Orden-Desorden

    Energy Technology Data Exchange (ETDEWEB)

    Dolling, G.; Gilat, G. [Chalk River Nuclear Laboratories, Chalk River, ON (Canada)

    1965-04-15

    Observations of normal modes of vibration of the ordered alloy of copper and zinc, {beta}-brass, at 296 Degree-Sign K have been made by means of the coherent one-phonon scattering of slow neutrons from single crystal specimens. The triple-axis crystal spectrometer at the NRU reactor has been used to measure the frequencies of modes propagating along the high-symmetry directions [00{zeta}], [{zeta}{zeta}0], [{zeta}{zeta}{zeta}{zeta}] and [ Vulgar-Fraction-One-Half Vulgar-Fraction-One-Half {zeta}]. The dispersion curves resemble those of a simple body-centred cubic crystal such as Na, except that certain degeneracies are lifted, mainly by reason of the difference between the second nearest neighbour Cu-Cu and Zn-Zn forces. For example, we find two distinct modes of wave vector (0.5, 0.5, 0.5) (in reciprocal lattice units), whose frequencies are (4.21 {+-}0.06) and (4.93 {+-} 0.10) x 10{sup 12} c/s respectively. Interatomic force models which provide a satisfactory description of the 296 Degree-Sign K results are briefly mentioned. Several normal modes have been studied at elevated temperatures, particularly in the vicinity of the order-disorder phase transition at about 727 Degree-Sign K. There are no striking changes in the overall structure of the dispersion curves as a result of the vanishing of the long range order at this temperature, although the various ''splittings'' observed at 296 Degree-Sign K are blurred out into more or less continuous ''bands'' of frequencies. As the temperature rises, the frequencies generally decrease, and the energy widths increase. These changes take place in a smooth manner, except for two longitudinal optic modes, observed at positions (1.27, 1.27, 0) and (1.2, 1.2, 0.2) in reciprocal space, which display sharp increases in energy width at the transition temperature. No reasonable explanation of these effects has yet been found. (author) [French] On a observe les modes normaux de vibration du laiton beta, alliage ordonne de cuivre

  9. Molecular CsF 5 and CsF 2 +

    KAUST Repository

    Rogachev, Andrey Yu.; Miao, Mao-sheng; Merino, Gabriel; Hoffmann, Roald

    2015-01-01

    D5h star-like CsF5, formally isoelectronic with known XeF5− ion, is computed to be a local minimum on the potential energy surface of CsF5, surrounded by reasonably large activation energies for its exothermic decomposition to CsF+2 F2, or to CsF3 (three isomeric forms)+F2, or for rearrangement to a significantly more stable isomer, a classical Cs+ complex of F5−. Similarly the CsF2+ ion is computed to be metastable in two isomeric forms. In the more symmetrical structures of these molecules there is definite involvement in bonding of the formally core 5p levels of Cs.

  10. Molecular CsF 5 and CsF 2 +

    KAUST Repository

    Rogachev, Andrey Yu.

    2015-06-03

    D5h star-like CsF5, formally isoelectronic with known XeF5− ion, is computed to be a local minimum on the potential energy surface of CsF5, surrounded by reasonably large activation energies for its exothermic decomposition to CsF+2 F2, or to CsF3 (three isomeric forms)+F2, or for rearrangement to a significantly more stable isomer, a classical Cs+ complex of F5−. Similarly the CsF2+ ion is computed to be metastable in two isomeric forms. In the more symmetrical structures of these molecules there is definite involvement in bonding of the formally core 5p levels of Cs.

  11. Evaluation of environmental radiological impact of {sup 137} Cs repository area, site of Abadia de Goias, using the RESRAD model; Avaliacao do impacto radiologico ambiental na area do repositorio de {sup 137} Cs, em Abadia de Goias, utilizando o modelo RESRAD

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira Loureiro, C. de [Minas Gerais Univ., Belo Horizonte, MG (Brazil). Escola de Engenharia; Aquino Branco, O.E. de [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN), Belo Horizonte, MG (Brazil)

    1995-12-31

    Radiological impacts under a conservative approach were assessed for the final deposition of {sup 137} Cs at the repository site of Abadia de Goias, in the State of Goias. This site was selected as the definitive storage location for the wastes generated in the radiological accident occurred in the definitive storage location for the wastes generated in the radiological accident occurred in the nearby city of Goiania, in September of 1987. The wastes are composed of various different materials, with an estimated radioactive inventory of about 1250 Ci of {sup 137} Cs, and will be deposited definitively in a repository box of concrete with a volume of 3900 m{sup 3} approximately. A conservative approach was considered in this study and the contaminated zone was simplified as an isotropic block of soil, of 3900 m{sup 3} of volume, containing 1250 Ci of {sup 137} Cs homogeneously distributed within the whole volume. Several potential exposure scenarios were considered for the assessment of the future radiological impacts predicted at the repository site, depending on the level of institutional control maintained at the site, its future use, the time spent at the site and the sources of food. A comparative analysis of the resulting radiological impacts from all these future potential scenarios was performed using a microcomputer program named RESRAD. The simulated results indicated that the external exposure to gamma radiation, directly from the contaminated soil, is the most significant exposure pathway. The maximum predicted annual dose was below 7 mrem. (author). 5 refs, 6 figs, 3 tabs.

  12. Treatment of wastes in the production of radioactive patterns of {sup 241}Am, {sup 137}Cs, {sup 57}Co e {sup 60}Co; Tratamento de rejeitos na producao de padroes radioativos de {sup 241}Am, {sup 137}Cs, {sup 57}Co e {sup 60}Co

    Energy Technology Data Exchange (ETDEWEB)

    Gomes, Regio dos Santos; Silva, Carlos Jose da; Veras, Eduardo Vieira de; Silva, Ronaldo Lins da; Poledna, Roberto; Laranjeiras, Adilson Silva; Delgado, Jose Ubiratan, E-mail: regio@ird.gov.br [Instituto de Radioprotecao e Dosimetria, (IRD/CNEN-RJ), Rio de Janeiro, RJ (Brazil). Lab. Nacional de Metrologia das Radiacoes Ionizantes

    2014-07-01

    Standardized sources of {sup 241}Am, {sup 137}Cs, {sup 57}Co and {sup 60}Co are the most requested solutions by customers of LNMRI. After preparation, the remainder of the stock is transferred to a new vial, with the generation of waste in glass and plastic pycnometers and high activity levels which can be recovered. By means of the rinse procedure, this work reduced the activity remaining for master solutions above 1 MBq/g. The treatment adopted here allowed to produce new standardized sources of radionuclides in the range of 20 to 70 kBq/g, with uncertainty below 3%, which may be offered to different users. (author)

  13. 137Cs in man organism

    International Nuclear Information System (INIS)

    Marej, A.N.; Barkhudarov, R.M.

    1980-01-01

    Considered are the levels of 137 Cs content in the organism of adult urban population of the USSR and the main regularities of their alterations during 1962-1974. The non-uniform distribution of levels of 137 Cs buildup in adult population is shown to be connected with soil and geographic conditions. Food stuffs of local production have a noticeable effect on the levels of 137 Cs buildup in the organism of urban population. Calculation methods are used to study 137 Cs administration in a human organism. No significant difference is found between the indexes of 137 Cs content in the organism of rural and urban population. Presented are the levels of 137 Cs content in the organisms of inhabitants of such regions as Far North and Byelorussian-Ukrainian woodlands. Given are the reasons for the increased content of 137 Cs in the organism of rural population of these zones

  14. Theoretical study of the Cs isotope exchange reaction of CsI + Cs' → Cs + ICs' (Contract research)

    International Nuclear Information System (INIS)

    Kobayashi, Takanori; Hashimoto, Masashi; Yokoyama, Keiichi

    2015-12-01

    To discuss the exchange reaction of Cs isotope by CsI + Cs' → Cs + ICs', the structure and chemical properties of Cs 2 I intermediate and potential energy surface of the entrance reaction are calculated using M06/def2-TZVPPD density functional calculation. The calculation shows that the reaction to the intermediate has no barrier and the two Cs-I bonds of Cs 2 I are chemically equivalent. These results suggest that the rate of the Cs exchange reaction of CsI + Cs' → Cs + ICs' is as high as the collision rate. (author)

  15. Frameworks in CS1

    DEFF Research Database (Denmark)

    Christensen, Henrik Bærbak; Caspersen, Michael Edelgaard

    2002-01-01

    In this paper we argue that introducing object-oriented frameworks as subject already in the CS1 curriculum is important if we are to train the programmers of tomorrow to become just as much software reusers as software producers. We present a simple, graphical, framework that we have successfull...... point for introducing graphical user interface frameworks such as Java Swing and AWT as the students are not overwhelmed by all the details of such frameworks right away but given a conceptual road-map and practical experience that allow them to cope with the complexity....

  16. CS Seminar Videos

    OpenAIRE

    Ong, Derek; Tona, Glen; Gibb, Kyle; Parbadia, Sivani

    2013-01-01

    Main site for our project can be found at this URL: http://vtechworks.lib.vt.edu/handle/10919/19036. From here you can find videos of all the CS seminars and distinguished lectures given this semester. Each video has its own abstract and description. The files attached in this section are a final report in both raw Word Document and archival PDF formats and a presentation in both raw Powerpoint and archival PDF formats. Computer Science seminars are a very educational and interesting as...

  17. Frameworks in CS1

    DEFF Research Database (Denmark)

    Christensen, Henrik Bærbak; Caspersen, Michael Edelgaard

    2002-01-01

    point for introducing graphical user interface frameworks such as Java Swing and AWT as the students are not overwhelmed by all the details of such frameworks right away but given a conceptual road-map and practical experience that allow them to cope with the complexity.......In this paper we argue that introducing object-oriented frameworks as subject already in the CS1 curriculum is important if we are to train the programmers of tomorrow to become just as much software reusers as software producers. We present a simple, graphical, framework that we have successfully...

  18. Adsorption of Cs{sup +}, Ni{sup 2+} and lanthanides onto a kaolinite and Na-montmorillonite up to 150{sup 0}C: an experimental and modeling study; Adsorption de Cs{sup +}, Ni{sup 2+} et des lanthanides sur une kaolinite et une smectite jusqu'a 150{sup 0}C: etude experimentale et modelisation

    Energy Technology Data Exchange (ETDEWEB)

    Tertre, E

    2005-10-15

    The motivation for this study is to assess the temperature effect on the clay minerals sorption properties. Sorption and desorption of Cs{sup +}, Ni{sup 2+} et Ln{sup 3+} onto a montmorillonite and a kaolinite were performed by batch experiments between 25 and 150 C, and in different pH and ionic strengths conditions. Sorption enthalpies varying between 0 and 80 kJ/mol were then calculated. For europium, surface spectroscopic analyses confirmed that the mechanism involved is adsorption, including at 150 C. Moreover, this method allowed us to obtain qualitatively the different adsorption equilibrium occurring during the reaction. An acid/base study of the clay surfaces was performed in order to assess the temperature effect on the surface charge of these minerals. Then, a surface complexation model including edge sites and structural sites was proposed to interpret the acid/base data and the europium sorption data. (author)

  19. Determination of Cs-134 and Cs-137 rain water samples

    International Nuclear Information System (INIS)

    Lima, M.F.; Mazzilli, B.

    1988-01-01

    In order to setting an environmental monitoring program at IPEN, was developed a fast and simple methodology for concentration of Cs-134 and Cs-137 in rain water. This procedure consists in the precipitation of cesium and others cathions of its family (NH 4 + , K + and Rb + ) by ammonium molybdophosphate. The measures of the desintegration rates of Cs-134 and Cs-137 was done by gamma spectrometry in a Ge(Li) detector. After setting up the ideal experimental conditions, the procedure was used to analyze four samples of rain water. (author) [pt

  20. Alkali metal and ammonium fluoro(trifluoroacetato)metallates M'[ M''3(μ3-F)(CF3COO)6(CF3COOH)3], where M' = Li, Na, K, NH4, Rb, or Cs and M'' = Ni or Co. Synthesis and crystal structures

    Science.gov (United States)

    Tereshchenko, D. S.; Morozov, I. V.; Boltalin, A. I.; Karpova, E. V.; Glazunova, T. Yu.; Troyanov, S. I.

    2013-01-01

    A series of fluoro(trifluoroacetato)metallates were synthesized by crystallization from solutions in trifluoroacetic acid containing nickel(II) or cobalt(II) nitrate hydrates and alkali metal or ammonium fluorides: Li[Ni3(μ3-F)(CF3COO)6(CF3COOH)3](CF3COOH)3 ( I), M'[Ni3(μ3-F)(CF3COO)6(CF3COOH)3] ( M' = Na ( II), NH4 ( IV), Rb ( V), and Cs ( VI)), NH4[Co3(μ3-F) (CF3COO)6(CF3COOH)3] ( III), and Cs[Ni3(μ3-F)(CF3COO)6(CF3COOH)3](CF3COOH)0.5 ( VII). The crystal structures of these compounds were determined by single-crystal X-ray diffraction. All structures contain triangular trinuclear complex anions [ M 3″(μ3-F)(CF3COO)6(CF3COOH)3]- ( M″ = Ni, Co) structurally similar to trinuclear 3d metal oxo carboxylate complexes. The three-coordinated F atom is located at the center of the triangle formed by Ni(II) or Co(II) atoms. The metal atoms are linked in pairs by six bridging trifluoroacetate groups located above and below the plane of the [ M″3 F] triangle. The oxygen atoms of the axial CF3COOH molecules complete the coordination environment of M″ atoms to an octahedron.

  1. Quaternary selenostannates Na{sub 2-x}Ga{sub 2-x}Sn{sub 1+x}Se{sub 6} and AGaSnSe{sub 4} (A=K, Rb, and Cs) through rapid cooling of melts. Kinetics versus thermodynamics in the polymorphism of AGaSnSe{sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Hwang, S -J; Iyer, R G; Kanatzidis, M G

    2004-10-01

    The quaternary alkali-metal gallium selenostannates, Na{sub 2-x}Ga{sub 2-x}Sn{sub 1+x}Se{sub 6} and AGaSnSe{sub 4} (A=K, Rb, and Cs), were synthesized by reacting alkali-metal selenide, Ga, Sn, and Se with a flame melting-rapid cooling method. Na{sub 2-x}Ga{sub 2-x}Sn{sub 1+x}Se{sub 6} crystallizes in the non-centrosymmetric space group C2 with cell constants a=13.308(3) A, b=7.594(2) A, c=13.842(3) A, {beta}=118.730(4) deg., V=1226.7(5) A{sup 3}. {alpha}-KGaSnSe{sub 4} crystallizes in the tetragonal space group I4/mcm with a=8.186(5) A and c=6.403(5) A, V=429.1(5) A{sup 3}. {beta}-KGaSnSe{sub 4} crystallizes in the space group P2{sub 1}/c with cell constants a=7.490(2) A, b=12.578(3) A, c=18.306(5) A, {beta}=98.653(5) deg., V=1705.0(8) A{sup 3}. The unit cell of isostructural RbGaSnSe{sub 4} is a=7.567(2) A, b=12.656(3) A, c=18.277(4) A, {beta}=95.924(4) deg., V=1741.1(7) A{sup 3}. CsGaSnSe{sub 4} crystallizes in the orthorhombic space group Pmcn with a=7.679(2) A, b=12.655(3) A, c=18.278(5) A, V=1776.1(8) A{sup 3}. The structure of Na{sub 2-x}Ga{sub 2-x}Sn{sub 1+x}Se{sub 6} consists of a polar three-dimensional network of trimeric (Sn,Ga){sub 3}Se{sub 9} units with Na atoms located in tunnels. The AGaSnSe{sub 4} possess layered structures. The compounds show nearly the same Raman spectral features, except for Na{sub 2-x}Ga{sub 2-x}Sn{sub 1+x}Se{sub 6}. Optical band gaps, determined from UV-Vis spectroscopy, range from 1.50 eV in Na{sub 2-x}Ga{sub 2-x}Sn{sub 1+x}Se{sub 6} to 1.97 eV in CsGaSnSe{sub 4}. Cooling of the melts of KGaSnSe{sub 4} and RbGaSnSe{sub 4} produces only kinetically stable products. The thermodynamically stable product is accessible under extended annealing, which leads to the so-called {gamma}-form (BaGa{sub 2}S{sub 4}-type) of these compounds.

  2. Crystal-structural study of zirconium chelates with alkali metals of composition A2[Zr(Nta)2]·xH2O (A=Li, Na, K, Rb, Cs or CH3H6)

    International Nuclear Information System (INIS)

    Sadikov, G.G.; Antsyshkina, A.S.; Sergienko, V.S.

    1997-01-01

    Some zirconium complexes with nitrile triacetate and with alkali metal in the external sphere were studied crystalostructurally. Packing of complexes and extra-sphere cations was studied. Plane or slightly corrugated anion layers of two essentially different types arranged according to the principle of trigonal and square grids represent the standard element of crystal structure. Water molecules are located both in anion and cation layers. CN and coordination polyhedron of cations are different even in case of stereotype nature of reasons of their location in the interlayer space. In Cs-, Rb- and K- compounds polyhedrons of alkali metal form specific doubled chains. These compounds are not isomorphous ones and are characterized by a specific way of water molecule location. Structure of sodium compound differs fundamentally from other ones. Ionic conductivity may be expected in crystals. 4 refs., 6 figs., 2 tabs

  3. Foundation Fireworks CS4

    CERN Document Server

    Smith, N; Heerema, Matt; Mallott, Chuch; King, R; Erskine, Craig

    2009-01-01

    Are you a web designer who is looking for a new and quicker way to prototype and create for the web? Perhaps you are a programmer who finds most design tools to be overkill for what you need to get done. Or, maybe you're an old Fireworks pro, who wants to keep up to date on the latest changes in Creative Suite 4. Either way, this book has something for you. * Coverage of all that's new and powerful for the Web designer and developer in Fireworks CS4* Targets developers who want design tools that don't get in their way and designers who want development tools that don't constrain their creativi

  4. Frameworks in CS1

    DEFF Research Database (Denmark)

    Christensen, Henrik Bærbak; Caspersen, Michael Edelgaard

    2002-01-01

    point for introducing graphical user interface frameworks such as Java Swing and AWT as the students are not overwhelmed by all the details of such frameworks right away but given a conceptual road-map and practical experience that allow them to cope with the complexity.......In this paper we argue that introducing object-oriented frameworks as subject already in the CS1 curriculum is important if we are to train the programmers of tomorrow to become just as much software reusers as software producers. We present a simple, graphical, framework that we have successfully...... used to introduce the principles of object-oriented frameworks to students at the introductory programming level. Our framework, while simple, introduces central abstractions such as inversion of control, event-driven programming, and variability points/hot-spots. This has provided a good starting...

  5. Erosion and sediment deposition evaluation on slopes under different tillage systems in the Cerrado region using the {sup 137}Cs fallout technique; Analise da distribuicao do fallout do {sup 137}Cs na avaliacao da erosao e deposicao de sedimentos em sistemas de manejo de solo sob Cerrado

    Energy Technology Data Exchange (ETDEWEB)

    Arthur, Robson Clayton Jacques

    2010-07-01

    In Brazil, the expansion of agricultural areas causes several problems on natural resources. With the increasing occupation of the Cerrado region by agriculture, a series of environmental problems like deforestation, soil erosion and soil compaction are appearing and causing radical transformations in the natural landscape due to removing almost all native vegetation. The conventional tillage system (CTS) is considered an inadequate form of soil management for its frequently irremediable consequences of soil compaction and soil erosion, and the no till system (NTS) makes the maintenance of the soil conditions possible, letting them close to the natural environment, thus reducing rates of soil erosion. The objective of this work was to evaluate the efficiency of riparian forests in the retention of sediments originated for three different tillage systems, through the fallout {sup 137}CS redistribution technique, the Universal Soil Loss Equation (USLE) and some physical and chemical parameters that indicate the structural conditions of the soils of Goiatuba and Jandaia-GO. In the three areas, soil profiles were collected in three layers of 20 cm (0-20, 20-40 and 40-60 cm) at distinct points located along linear transects in the direction of the maximum slope until the riparian forest. In the riparian forest of each area, trenches were opened and soil was sampled to evaluate the activity of {sup 137}Cs and the physical and chemical parameters of soil. Detection of the activity of {sup 137}Cs was made with a gamma ray detector model (GEM-20180P, EG and ORTEC) connected to a multichannel analyzer. The comparison of averages was made using the Tukey test at 5% level of significance. The. results indicated that, the three soil tillage systems presented high rates of soil erosion and deposition of sediments and the riparian forest of the areas under CTS, NTS and pasture, located downstream received great amounts of sediments, and that only the riparian forest of CTS was

  6. Variability in uptake of Cs isotopes by fenugreek plant from three soils

    Energy Technology Data Exchange (ETDEWEB)

    Pulhani, V; Dafauti, S; Dahiya, S; Hedge, A G [Environmental Studies Section, Health Physics Div., Bhabha Atomic Research Centre, Mumbai (India)

    2008-07-01

    Soil to plant transfer via root uptake is one of the major compartments in the radionuclide transfer pathways to man and can be used to assess the internal radiation dose via ingestion. The variability in the Transfer Factor (TF) of Cs isotopes was investigated in three different soils from nuclear power plant sites at Rajasthan and Narora with alkaline sandy loam alluvial and Madras with acidic coastal sandy loam alluvial soil. The soils were characterized for soil properties like texture, pH, EC, organic carbon, CaCO{sub 3} (%), CEC, silt, clay sand etc. and spiked with a mixture of 800 Bq {sup 137}Cs, 300 Bq {sup 134}Cs and 10mg of {sup 133}Cs (stable). Fenugreek (Trigonella foenum-graecum L.) from Leguminosae family an annual plant commonly used as a vegetable was grown in these soils to study the uptake of Cs. The uptake of heavy toxic elements like Pb, Cd, Ni, Cr etc. and nutrients Fe, Co, Cu, Zn, Mn, Ca, Mg, Na and K was also studied. The uptake of heavy toxic elements like Pb, Cd, Ni, Cr etc. and nutrients Fe, Co, Cu, Zn, Mn, Ca, Mg, Na and K was also studied. {sup 137}Cs and{sup 134}Cs was estimated using HPGe detector (15% Relative Efficiency, 54cc-coaxial, 2keV resolution at 1332keV of {sup 60}Co). Stable Cs, K and Na were determined by the Atomic Emission Spectrophotometry and Pb, Cd, Cr etc. by Atomic Absorption Spectrophotometry. Among the three soils the transfer factor for all the elements and Cs was highest for MAPS due to higher organic matter content and acidic pH followed by NAPS and RAPS. The {sup 137}Cs and {sup 134}Cs isotopes have been taken up to the same extent from soil and transfer factors are similar to each other. But the stable Cs uptake appears to be slightly high, probably because of excess of {sup 133}Cs (mg level) added as compared to the radioactive isotopes. In spite of this high difference in the soil concentrations of Cs isotopes, uptake of {sup 133}Cs is not very high indicating to a physiological limiting process for uptake

  7. The chemical speciation of 137Cs in sheepmeat

    International Nuclear Information System (INIS)

    Pang, T.Y.M.; Taylor, D.M.; Williams, D.R.

    1996-01-01

    Minced sheep muscle, homogenised liver and fragmented rib or cortical bone, from sheep grazing near Bootle, Cumbria, U.K., which had been stored for some months at -20 o C, were extracted at 4 o C with an isotonic 0.15 M NaCl-0.02 M phosphate buffer at pH 7.4. Each successive extraction released about 50% of the total 137 Cs remaining in the tissue. Passage of the extracts through a column of the cation-exchanger Dowex 50 x 8 indicated that essentially all the extracted 137 Cs was in cationic form. (author)

  8. O tema da morte trágica de Liev Tolstói e seu impacto em Max Weber e György Lukács: sobre a autonomia nas ciências e na arte * Leo Tolstoy´s tragic death and his impacts on Max Weber and György Lukács: on autonomy of arts and science

    Directory of Open Access Journals (Sweden)

    LUIS FELIPE DE SALLES ROSELINO

    2014-04-01

    Full Text Available Resumo: O tema da morte trágica, presente nos escritos de Liev Tolstói, auxiliou tanto a Max Weber como a György Lukács a caracterizarem o pathos moderno de pressentimento da morte como uma contemplação do vazio. Weber e Lukács encontraram, através das leituras de Tolstói, uma interessante maneira de questionar a autonomia da arte e da ciência moderna, considerando pela esfera estética, como se mostra sem sentido a recente realidade imanente. Ambos assumiram o tema central das obras de Tolstói segundo uma mesma imagem, derivada do contraste entre o mundo antigo e o moderno. Max Weber adequou esse tema a sua teoria do desencantamento do mundo e Lukács, de modo muito semelhante, seguindo seu conceito do paradoxo da necessidade religiosa.Palavras-chave: Tolstói – Weber – Lukács – Desencantamento – Necessidade Religiosa – L’Art Pour l’Art. Abstract: The tragic death in Tolstoy's writings has helped both Max Weber and György Lukács in characterizing the modern pathos as a tragic contemplation of the emptiness of life. Through Tolstoy's readings, Weber and Lukács found an interesting source of denying arts and modern sciences autonomy, considering, from the aesthetics sphere, the meaningless of this new immanent reality. Both has assumed Tolstoy main theme from the same perspective, contrasting ancient and modern worldviews. Max Weber presented this theme in his disenchantment of world theory and Lukács, in a very similar way, following the paradox of religious needing as a mainline.Keywords: Tolstoy – Weber – Lukács – Disenchantment – Religious Needing – L’Art Pour l’Art.

  9. 1+ collective states of 124Cs and 126Cs nuclei

    International Nuclear Information System (INIS)

    Ivanova, S.P.; Kuliev, A.A.; Salamov, D.I.

    1977-01-01

    Within the framework of the random phase approximation β-decay properties of the 1 + states of 124 Cs and 126 Cs have been investigated. Greatly collectivized 1 + states in odd-odd nuclei are produced by the spin-dependent charge-exchange nucleon interaction. For numerical calculations the scheme of single-particle levels in the deformed Saxon-Woods potential has been used

  10. Fission product behavior in high-temperature water: CsI vs MoO4

    Science.gov (United States)

    Kanjana, K.; Silva, K.; Channuie, J.

    2017-09-01

    Fission product behaviors of Cs, a major element released in a severe nuclear accident, still remain unclear. The question frequently addressed is whether Cs released will be in the form of Cs2MoO4 or CsOH. This is a challenging issue since it has been demonstrated that the reaction between Cs2MoO4 and water leading to CsOH production is thermodynamically favored. The present research aims at investigation of CsOH generation through this chemical channel. A high-temperature setup with a flow system based on the cooling system of a water-cooled nuclear reactor has been assembled. The reaction between aqueous solutions of CsI and Na2MoO4 in a high-corrosion-resistant hot cell (Hastelloy) has been studied up to 80 °C in deoxygenated system. The products have been characterized using FTIR and XRD. The results have shown that there is no reaction between CsI and Na2MoO4 under the experimental conditions.

  11. Learning Flash CS4 Professional

    CERN Document Server

    Shupe, Rich

    2009-01-01

    Learning Flash CS4 Professional offers beginners and intermediate Flash developers a unique introduction to the latest version of Adobe's powerful multimedia application. This easy-to-read book is loaded with full-color examples and hands-on tasks to help you master Flash CS4's new motion editor, integrated 3D system, and character control using the new inverse kinematics bones animation system. No previous Flash experience is necessary.

  12. Characterization of sorption properties of modified biosorbents for preconcentration of 137Cs

    International Nuclear Information System (INIS)

    Dulanska, S.; Petercova, S.; Matel, L.

    2017-01-01

    In the work the biosorbent was modified for preconcentration of 137 Cs in aqueous solutions. For an impregnation the biosorbent made of wood-decay fungus - Fomes fomentarius was used. The properties of the impregnated biosorbent were studied in model solutions with the addition of 137 Cs. It was found, that the biosorbent had a high absorbability of 137 Cs in the wide range of pH, even in the solutions with high ionic strength. The maximum sorption capacity of the biosorbent was 50 mg Cs + /g. The effect of competing ions Na + , K + , Ca 2+ and Mg 2+ was tested. It was found, that the tested cations didn't have a significant effect on the sorption of 137 Cs. It was found, that the most suitable medium for the elution of 137 Cs from biosorbent is HNO 3 with a concentration higher than 7 mol · dm -3 . (authors)

  13. Sorption Analysis of 137Cs On Karawang’s Clay Samples

    Directory of Open Access Journals (Sweden)

    Budi Setiawan

    2016-12-01

    Full Text Available The objective of this work is to characterize the specific of distribution coefficient (Kd values of 137Cs onto Karawang’s clay for radioactive waste disposal facility purpose. Sorption phenomena was affected by contact time, ionic strength and loaded concentration of CsCl.  Experiments were done in a batch method, with initial concentration was 10-8 M CsCl in the experiments of contact time and ionic strength effects. In the CsCl loading experiment, the concentration was varied from 10-8 to 10-4 M CsCl and 137Cs radioactive solution was used as a tracer. The solid-liquid ratio is 10-2 g/mL.  The results shown that obtained Kd values were 21,714 and 4035 mL/g after contacted for 8 days for Sample-1 and 2, respectively. The presence of K+ and Na+ ions in solution had reduced the Kd value Cs-137 where the effect of K+ is greater than Na+ on decreased the value of Kd.  The increasing of CsCl concentrations in solution had reduced the value of Kd.  In both samples of clay were closely fit to Freundlich isotherm and pseudo-second order kinetic model.  The results are very useful as the input of the safety assessment activity of site candidate for radioactive waste disposal facility in the future.

  14. Salt-stimulation of caesium accumulation in the euryhaline green microalga Chlorella salina: potential relevance to the development of a biological Cs-removal process

    Energy Technology Data Exchange (ETDEWEB)

    Avery, S. V.; Codd, G. A.; Gadd, G. M. [Department of Biological Sciences, University of Dundee, Dundee DD1 4HN (United Kingdom)

    1993-07-01

    Accumulation of Cs{sup +} by Chlorella salina was 28-fold greater in cells incubated in the presence than in the absence of 0.5 M-NaCl. An approximate 70% removal of external Cs{sup +} resulted after 15 h incubation of cells with 50 μ;M-CsCl and 0.5 M-NaCl. LiCl also had a stimulatory effect on Cs{sup +} uptake, although mannitol did not. Cs{sup +} influx increased with increasing external NaCl concentration and was maximal between 25-500 mM-NaCl at approximately 4 nmol Cs{sup +} h−1 (10{sup 6} cells){sup −1}. Little effect on Cs{sup +} uptake resulted from the presence of Mg{sup 2+} or Ca{sup 2+} or from varying the external pH, and Cs{sup +} was relatively non-toxic towards C. salina. At increasing cell densities (from 4 × 10{sup 5} to 1 × 10{sup 7} cells ml{sup +1}), decreasing amounts of Cs{sup +} were accumulated per cell although the rate of Cs{sup +} removal from the external medium was still greatest at the higher cell densities examined. Freely suspended C. salina and cell-loaded alginate microbeads accumulated similar levels of Cs{sup +}, however, 46% of total Cs{sup +} uptake was attributable to the calcium-alginate matrix in the latter case. When Cs{sup +}-loaded cells were subjected to hypoosmotic shock, loss of cellular Cs{sup +} occurred allowing easy Cs{sup +} recovery. This loss exceeded 90% of cellular Cs{sup +} when cells were washed with solutions containing ≤ 50 mM-NaCl between consecutive Cs{sup +} uptake periods; these cells subsequently lost their ability to accumulate large amounts of Cs{sup +}. Maximal Cs{sup +} uptake (approximately 85.1% removal after three 15 h incubations) occurred when cells were washed with a solution containing 500 mM-NaCl and 200 mM-KCl between incubations. The relevance of these results to the possible use of C. salina in a salt-dependent biological Cs-removal process is discussed. (author)

  15. Application of in-situ measurement to determine 137Cs in the Swiss Alps

    International Nuclear Information System (INIS)

    Schaub, M.; Konz, N.; Meusburger, K.; Alewell, C.

    2010-01-01

    Establishment of 137 Cs inventories is often used to gain information on soil stability. The latter is crucial in mountain systems, where ecosystem stability is tightly connected to soil stability. In-situ measurements of 137 Cs in steep alpine environments are scarce. Most studies have been carried out in arable lands and with Germanium (Ge) detectors. Sodium Iodide (NaI) detector system is an inexpensive and easy to handle field instrument, but its validity on steep alpine environments has not been tested yet. In this study, a comparison of laboratory measurements with GeLi detector and in-situ measurements with NaI detector of 137 Cs gamma soil radiation has been done in an alpine catchment with high 137 Cs concentration (Urseren Valley, Switzerland). The aim of this study was to calibrate the in-situ NaI detector system for application on steep alpine slopes. Replicate samples from an altitudinal transect through the Urseren Valley, measured in the laboratory with a GeLi detector, showed a large variability in 137 Cs activities at a meter scale. This small-scale heterogeneity determined with the GeLi detector is smoothed out by uncollimated in-situ measurements with the NaI detector, which provides integrated estimates of 137 Cs within the field of view (3.1 m 2 ) of each measurement. There was no dependency of 137 Cs on pH, clay content and carbon content, but a close relationship was determined between measured 137 Cs activities and soil moisture. Thus, in-situ data must be corrected for soil moisture. Close correlation (R 2 = 0.86, p 137 Cs activities (in Bq kg -1 ) estimated with in-situ (NaI detector) and laboratory (GeLi detector) methods. We thus concluded that the NaI detector system is a suitable tool for in-situ measurements in alpine environments. This paper describes the calibration of the NaI detector system for field application under elevated 137 Cs activities originating from Chernobyl fallout.

  16. The Concentration of Cs-137 Pollutan in Water Pumps in Several Cities of Java Island

    International Nuclear Information System (INIS)

    Nareh, M; Warsono, A; Indiyati, T; Yurfida; Buchari

    1996-01-01

    The aim of this research is to know the concentration of Cs-137 in the water pumps. The concentration of Cs-137 pollutant in the water pumps from 10 cities in Java Island had been determined. Cs-137 in big volume of water was collected in cation exchanger and eluted with 6N HCl solution. Cs-137 in the eluen was precipitated by ammoniumphosphomolybdate (AMP), soluted using NaOH solution and finally measured using Spectrometer Gamma Canberra 35 Plus with high pure germanium detector (HPGe). The results of measurement indicate that the concentration of cs-137 in the tested water pumps are in the range of under minimum detectable (BDT) to 2,06 + 0,79 mBq/I

  17. Adsorption characteristics of Cs"+ onto artificial zeolites synthesized from coal fly ash and diatomite

    International Nuclear Information System (INIS)

    Johan, Erni; Yoshida, Kohei; Itagaki, Yoshiteru; Aono, Hiromichi; Munthali, Moses Wazingwa; Matsue, Naoto

    2015-01-01

    The radioactive decontamination of water, soil and other materials requires cheap and effective adsorbents. Artificial zeolites synthesized from an industrial waste (coal fly ash: Na-P1 type zeolite) and a natural material (diatomite: mordenite type zeolite) have a high Cs"+ adsorptivity in the adsorption experiments using 0.1 g of the zeolite and 50 mL of up to 7.5 mM CsCl. The coexisting cation suppressed the Cs"+ adsorption onto the zeolites, and the effect of the suppression was in the order, K"+ > Na"+ > Ca"2"+ > Mg"2"+. A thermodynamic analysis proved that the Cs"+ adsorption onto the two zeolites was exothermic favoring a lower temperature. The artificial mordenite showed a greater Cs"+ adsorption strength, higher distribution coefficient and lower ΔG°, especially at low Cs"+ concentrations. Adsorption isotherm analysis by the Langmuir, Freundlich, Temkin and Dubinin-Radushkevich models showed a greater Cs"+ adsorption selectivity for the artificial mordenite even at a low pH. (author)

  18. 'Wash-out' of Cs-134 and Cs-137 from river sediment; 'Ispiranja' Cs-134 i Cs-137 iz recnog sedimenta

    Energy Technology Data Exchange (ETDEWEB)

    Skrbic, Z; Conkic, Lj; Bikit, I; Veskovic, M; Slivka, J; Marinkov, L [Institut za Fiziku, Novi Sad Univ. (Yugoslavia)

    1988-07-01

    Natural elimination and 'wash out' period of the Cs-134 and Cs-137 from the river sediment has been investigated. Obtained results suggest the possibility to describe these processes by exponential low and determination of the corresponding half lives. (author)

  19. Growth of PbX2 and CsPbX3 (X = Cl, Br) mesoscopic phases in alkali halide host lattices

    Science.gov (United States)

    Polak, K.; Nitsch, K.; Nikl, M.

    Formation of PbCl2 and CsPbBr3 microphases in NaCl and CsBr respectively is studied using mainly an absorption spectroscopy. The absorption of NaCl: Pb crystal was investigated as a function of annealing temperature and duration of thermal treatment. Changes in the position and shape of the exciton band were studied in CsBr: Pb absorption spectrum. The results showed that the shape of CsPbBr3 microcrystals is far from a spherical one. The microcrystals probably grow as highly elongated discs.

  20. Uptake and distribution of 137Cs, stable Cs and K in rice plants

    International Nuclear Information System (INIS)

    Tsukada, Hirofumi; Hasegawa, Hidenao

    2003-01-01

    The uptake and distributions of 137 Cs, stable Cs and K were determined for rice plant components, including polished rice, rice bran, hulls, leaves, stems, and roots. The distribution of 137 Cs in polished rice and rice bran was similar to that of stable Cs, while that of K was different. The concentration ratios of Cs/K in leaves increased in older leaf blade positions, which meant that the translocation rate of stable Cs, was slower than that of K. At harvest the dry weight of polished rice accounted for 34% of the entire rice plant, while the distributions of stable Cs in the polished rice and the non-edible parts were 7 and 93%, respectively. These findings suggest that the transfer and distribution of stable Cs in rice plants are different from those of K, and the behavior of stable Cs provides a useful analogue in predicting the fate of 137 Cs in an agricultural environment. (author)

  1. New compounds bearing [M(S_2O_7)_3]"2"- anions (M = Si, Ge, Sn): Syntheses and characterization of A_2[Si(S_2O_7)_3] (A = Na, K, Rb), A_2[Ge(S_2O_7)_3] (A = Li, Na, K, Rb, Cs), A_2[Sn(S_2O_7)_3] (A = Na, K), and the unique germanate Hg_2[Ge(S_2O_7)_3]Cl_2 with cationic "1_∞[HgCl_2_/_2]"+ chains

    International Nuclear Information System (INIS)

    Logemann, Christian; Witt, Julia; Wickleder, Mathias S.; Gunzelmann, Daniel; Senker, Juergen

    2012-01-01

    The reaction of the group 14 tetrachlorides MCl_4 (M = Si, Ge, Sn) with oleum (65 % SO_3) at elevated temperatures led to the unique anionic complexes [M(S_2O_7)_3]"2"- that show the central M atoms in coordination of three chelating S_2O_7"2"- groups. The mean distances M-O within the complexes increase from 175 pm (M = Si) via 186 pm (M = Ge) up to 200 pm (M = Sn). The charge balance for the [M(S_2O_7)_3]"2"- anions is achieved by alkaline metal ions A"+ (A = Li, Na, K, Rb, Cs) which were implemented in the syntheses in form of their sulfates. The size of the A"+ ions, i.e. their coordination requirement causes the crystallographic differences in the crystal structures, while the structure of the complex [M(S_2O_7)_3]"2"- anions remains essentially unaffected. Furthermore, we were able to characterize the unique germanate Hg_2[Ge(S_2O_7)_3]Cl_2 which forms when HgCl_2 is added as a source for the counter cation. The Hg"2"+ and the Cl"- ions form infinite cationic chains according to "1_∞[HgCl_2_/_2]"+ which take care for the charge compensation. For selected examples of the compounds the thermal behavior has been monitored by means of thermal analyses and X-ray powder diffraction. For A being an alkaline metal the decomposition product is a mixture of the sulfates A_2SO_4 and the dioxides MO_2, whereas Hg_2[Ge(S_2O_7)_3]Cl_2 shows a more complicated decomposition. The tris-(disulfato)-silicate Na_2[Si(S_2O_7)_3] has additionally been examined by solid state "2"9Si and "2"3Na NMR spectroscopic measurements. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  2. Adobe Photoshop CS6 bible

    CERN Document Server

    Dayley, Brad

    2012-01-01

    The comprehensive, soup-to-nuts guide to Photoshop, fully updated Photoshop CS6, used for both print and digital media, is the industry leader in image-editing software. The newest version adds some exciting new features, and this bestselling guide has been revised to cover each of them, along with all the basic information you need to get started. Learn to use all the tools, including the histogram palette, Lens Blur, Match Color, and the color replacement tool, as well as keyboard shortcuts. Then master retouching and color correction, work with Camera Raw images, prepare photos for print

  3. Reactive barriers for 137Cs retention

    International Nuclear Information System (INIS)

    Krumhansl, James L.; Brady, Patrick V.; Anderson, Howard L.

    2000-01-01

    137 Cs was dispersed globally by cold war activities and, more recently, by the Chernobyl accident. Engineered extraction of 137 Cs from soils and groundwaters is exceedingly difficult. Because the half life of 137 Cs is only 30.2 years, remediation might be more effective (and less costly) if 137 Cs bioavailability could be demonstrably limited for even a few decades by use of a reactive barrier. Essentially permanent isolation must be demonstrated in those few settings where high nuclear level wastes contaminated the environment with 135 Cs (half life 2.3x10 6 years) in addition to 137 Cs. Clays are potentially a low-cost barrier to Cs movement, though their long-term effectiveness remains untested. To identify optimal clays for Cs retention Cs resorption was measured for five common clays: Wyoming Montmorillonite (SWy-1), Georgia Kaolinites (KGa-1 and KGa-2), Fithian Illite (F-Ill), and K-Metabentonite (K-Mbt). Exchange sites were pre-saturated with 0.16 M CsCl for 14 days and readily exchangeable Cs was removed by a series of LiNO 3 and LiCl washes. Washed clay were then placed into dialysis bags and the Cs release to the deionized water outside the bags measured. Release rates from 75 to 139 days for SWy-1, K-Mbt and F- 111 were similar; 0.017 to 0.021% sorbed Cs released per day. Both kaolinites released Cs more rapidly (0.12 to 0.05% of the sorbed Cs per day). In a second set of experiments, clays were doped for 110 days and subjected to an extreme and prolonged rinsing process. All the clays exhibited some capacity for irreversible Cs uptake so most soils have some limited ability to act as a natural barrier to Cs migration. However, the residual loading was greatest on K-Mbt (∼ 0.33 wt% Cs). Thus, this clay would be the optimal material for constructing artificial reactive barriers

  4. Cs+ and Sr2+ adsorption selectivity of zeolites in relation to radioactive decontamination

    Directory of Open Access Journals (Sweden)

    M.W. Munthali

    2015-09-01

    Full Text Available Zeolites are used as adsorbents of cationic elements in the radioactive decontamination process of water, soil and others. We determined Cs+ and Sr2+ adsorption selectivity of some zeolites to know effective zeolite species for the decontamination of radioactive Cs and Sr. A 30 mL mixed solution containing up to 15 mg L−1 of non-radioactive Cs+ or Sr+ and up to 0.50 M of Na+ or K+ was mixed with 0.5 g of Linde-type A, Na-P1, faujasite X, faujasite Y and mordenite. Among the zeolites, mordenite had the highest Cs+ adsorption selectivity, and the selectivity had no correlation to the cation exchange capacity (CEC of the zeolites. In contrast, Sr2+ adsorption selectivity of the zeolites positively correlated with the CEC of the zeolites; Linde-type A with the highest CEC showed the highest adsorption selectivity, and its adsorption rate was more than 99.9% even in the presence of 0.5 M K+. A simulated soil decontamination experiment of Cs from a Cs-retaining vermiculite by using mordenite and that of Sr from a Sr-retaining vermiculite by using Linde-type A showed decontamination rates of more than 90%.

  5. Determination of {sup 135}Cs and {sup 137}Cs in environmental samples: A review

    Energy Technology Data Exchange (ETDEWEB)

    Russell, B.C., E-mail: ben.russell@npl.co.uk [GAU-Radioanalytical, Ocean and Earth Science, University of Southampton, National Oceanography Centre, Southampton, SO14 3ZH (United Kingdom); National Physical Laboratory, Hampton Road, Teddington, Middlesex, TW11 0LW (United Kingdom); Croudace, Ian W.; Warwick, Phil E. [GAU-Radioanalytical, Ocean and Earth Science, University of Southampton, National Oceanography Centre, Southampton, SO14 3ZH (United Kingdom)

    2015-08-26

    Radionuclides of caesium are environmentally important since they are formed as significant high yield fission products ({sup 135}Cs and {sup 137}Cs) and activation products ({sup 134}Cs and {sup 136}Cs) during nuclear fission. They originate from a range of nuclear activities such as weapons testing, nuclear reprocessing and nuclear fuel cycle discharges and nuclear accidents. Whilst {sup 137}Cs, {sup 134}Cs and {sup 136}Cs are routinely measurable at high sensitivity by gamma spectrometry, routine detection of long-lived {sup 135}Cs by radiometric methods is challenging. This measurement is, however, important given its significance in long-term nuclear waste storage and disposal. Furthermore, the {sup 135}Cs/{sup 137}Cs ratio varies with reactor, weapon and fuel type, and accurate measurement of this ratio can therefore be used as a forensic tool in identifying the source(s) of nuclear contamination. The shorter-lived activation products {sup 134}Cs and {sup 136}Cs have a limited application but provide useful early information on fuel irradiation history and have importance in health physics. Detection of {sup 135}Cs (and {sup 137}Cs) is achievable by mass spectrometric techniques; most commonly inductively coupled plasma mass spectrometry (ICP-MS), as well as thermal ionisation (TIMS), accelerator (AMS) and resonance ionisation (RIMS) techniques. The critical issues affecting the accuracy and detection limits achievable by this technique are effective removal of barium to eliminate isobaric interferences arising from {sup 135}Ba and {sup 137}Ba, and elimination of peak tailing of stable {sup 133}Cs on {sup 135}Cs. Isobaric interferences can be removed by chemical separation, most commonly ion exchange chromatography, and/or instrumental separation using an ICP-MS equipped with a reaction cell. The removal of the peak tailing interference is dependent on the instrument used for final measurement. This review summarizes and compares the analytical procedures

  6. Evaluation and testing of HUMASORB-CS trademark for the removal of radionuclides from groundwater

    International Nuclear Information System (INIS)

    Mann, N.R.; Todd, T.A.; Wood, D.J.

    1998-01-01

    An independent experiment to demonstrate the combined removal of the radionuclides, 85 Sr and 137 Cs from groundwater has been conducted with the sorbent, HUMASORB-CS. Arctech, Inc. manufactures this humic acid-based sorbent material. This sorbent material is reported to have potential for remediation of contaminated groundwater present at DOE sites. The purpose of this work was to evaluate the removal efficiency and the capacity of the sorbent. Two ion-exchange columns were assembled at the Idaho Chemical Processing Plant (ICPP) to evaluate the sorbent technology. Initial 137 Cs breakthrough in both columns was observed after 22.0 and 30.2 bed volumes, respectively. Strontium-85 removal was slightly more efficient than 137 Cs removal. Initial 85 Sr breakthrough in both columns was observed after 29.4 and 22.7 bed volumes, respectively. Calcium, which is of concern, is the major constituent within the feed solution. Calcium is attributed to loading interference in addition to other alkaline and alkaline earth metals such as stable Sr, Mg, Na, K, and Ba. Interfering ions fill exchange sites that greatly reduce the sorbents efficiency to sorb targeted ions such as radioactive Cs and Sr. Despite high concentrations of Ca in the feed solution, Ca was not sorbed by HUMASORB-CS. Results indicate HUMASORB-CS does not sorb sodium or potassium. Sodium and potassium concentrations were consistently observed at 100% breakthrough throughout the test

  7. Cs-137 migration in soil near NPPs

    International Nuclear Information System (INIS)

    Silant'ev, A.N.; Shkuratova, I.G.; Khatskevich, R.N.

    1984-01-01

    A convective-diffusion model has been employed for describing Cs-137 migration in soil. The migration parameters were determined by comparing the calculated vertical distribution profiles with the experimental ones. The migration parameters dependence on the soil state has been studied. Cs-137 penetration rate was found to be function of the soil type, surface state, soil wetness and orography. The obtained values are presented. A method is suggested for revealing the soil surface contamination by Cs-137 produced during NPP operation with distinguishing it from the global contamination background. For this purpose Cs-137 content in the upper 5 mm soil layer is estimated [ru

  8. {sup 137}Cs sorption into bentonite from Cidadap-Tasikmalaya as buffer material for disposal demonstration plant facility at Serpong

    Energy Technology Data Exchange (ETDEWEB)

    Setiawan, B., E-mail: bravo@batan.go.id; Sriwahyuni, H., E-mail: bravo@batan.go.id; Ekaningrum, NE., E-mail: bravo@batan.go.id; Sumantry, T., E-mail: bravo@batan.go.id [Radwaste Technology Center-National Nuclear Energy Agency, PUSPIPTEK, Serpong-Tangerang 15310 (Indonesia)

    2014-03-24

    According to co-location principle, near surface disposal type the disposal demonstration plant facility will be build at Serpong nuclear area. The facility also for anticipation of future needs to provide national facility for the servicing of radwaste management of non-nuclear power plant activity in Serpong Nuclear Area. It is needs to study the material of buffer and backfill for the safety of demonstration plant facility. A local bentonite rock from Cidadap-Tasikmalaya was used as the buffer materials. Objective of experiment is to find out the specific data of sorption characteristic of Cidadap bentonite as buffer material in a radwaste disposal system. Experiments were performed in batch method, where bentonite samples were contacted with CsCl solution labeled with Cs-137 in 100 ml/g liquid:solid ratio. Initial Cs concentration was 10{sup −8} M and to study the effects of ionic strength and Cs concentration in solution, 0.1 and 1.0 M NaCl also CsCl concentration ranging 10{sup −8} - 10{sup −4} M were added in solution. As the indicator of Cs saturated in bentonite samples, Kd value was applied. Affected parameters in the experiment were contact time, effects of ionic strength and concentration of CsCl. Results showed that sorption of Cs by bentonite reached constantly after 16 days contacted, and Kd value was 10.600 ml/g. Effect of CsCl concentration on Kd value may decreased in increased in CsCl concentration. Effect of ionic strength increased according to increased in concentration of background and would effect to Kd value due to competition of Na ions and Cs in solution interacts with bentonite. By obtaining the bentonite character data as buffer material, the results could be used as the basis for making of design and the basic of performance assessment the near surface disposal facility in terms of isolation capacity of radwaste later.

  9. Scintillation detector composed by new type of avalanche photodiode and CsI(Tl) crystal

    International Nuclear Information System (INIS)

    He Jingtang; Chen Duanbao; Li Zuhao; Mao Yufang; Dong Xiaoli

    1996-01-01

    Using S5345 type of avalanche photodiode produced by Hamamatsu for the CsI(Tl) crystal readout, the spectrum of γ ray were measured. Energy resolution of 6.8% for 1.27 MeV γ ray from 22 Na source was obtained. The relation between energy resolution and coupling area, dimension of crystal, shaping time and bias were measured

  10. Chemical kinetics of Cs species in an alkali-activated municipal solid waste incineration fly ash and pyrophyllite-based system using Cs K-edge in situ X-ray absorption fine structure analysis

    Science.gov (United States)

    Shiota, Kenji; Nakamura, Takafumi; Takaoka, Masaki; Nitta, Kiyofumi; Oshita, Kazuyuki; Fujimori, Takashi; Ina, Toshiaki

    2017-05-01

    We conducted in situ X-ray absorption fine structure (in situ XAFS) analysis at the Cs K-edge to investigate the chemical kinetics of Cs species during reaction in an alkali-activated municipal solid waste incineration fly ash (MSWIFA) and pyrophyllite-based system. Understanding the kinetics of Cs is essential to the design of appropriate conditions for Cs stabilization. In situ XAFS analysis of four pastes, prepared from NaOHaq, sodium silicate solution, pyrophyllite, and MSWIFA with the addition of CsCl, was conducted in custom-built reaction cells at four curing temperatures (room temperature, 60 °C, 80 °C, 105 °C) for approximately 34 h. The results indicated that the change in Cs species during reaction at room temperature was small, while changes at higher temperatures were faster and more extreme, with the fastest conversion to pollucite occurring at 105 °C. Further analysis using a leaching test and a simple reaction model for Cs species during reaction showed that the pollucite formation rate was dependent on the curing temperature and had a significant negative correlation with Cs leaching. The activation energy of pollucite formation was estimated to be 31.5 kJ/mol. These results revealed that an important change in the chemical state of Cs occurs during reaction in the system.

  11. Analysis of 137Cs in fission based neutron dosimetry

    International Nuclear Information System (INIS)

    Peltonen, T.

    1995-11-01

    137 Cs analysis is based on dissolving an irradiated fission dosimeter and chemically separating the cesium from the rest of the fission material. The samples consisted of uranium and neptunium in the form of metal or oxide. The uranium samples were dissolved in nitric acid and the neptunium samples in a mixture of nitric acid and chloric acid with addition of hydrogen peroxide. Cs was precipitated into a mixture of ammonium molyndophoshate and cellulose powder. A preparate for measurement was made from the precipitate and covered with polyethen plastic. Since other fission products than cesium were precipitated as well from the more recently irradiated samples, the activity measurements could not be carried out with a NaI(Tl) cavity crystal, but had to be made with a less efficient but more selective germanium semiconductor crystal. The method is well suited for 137 Cs determination, especially for older dosimeters where the more short-lived fission products have decayed. (orig.) (6 refs., 7 figs., 7 tabs.)

  12. Properties of Cs-intercalated single wall carbon nanotubes investigated by 133Cs Nuclear Magnetic resonance

    KAUST Repository

    Schmid, Marc R.; Mahfouz, Remi; Bouhrara, Mohamed; Saih, Youssef; Mehring, Michael; Basset, Jean-Marie; Goze-Bac, Christophe; Abou-Hamad, Edy

    2012-01-01

    present within the carbon nanotube bundles. At high concentrations, the Cs (β)+ ions seem to occupy well defined positions relative to the carbon lattice. As a matter of fact, the Korringa relaxation behavior suggests a strong hyperfine coupling between Cs

  13. Temperature and Pressure Dependence of the Reaction S plus CS (+M) -> CS2 (+M)

    DEFF Research Database (Denmark)

    Glarborg, Peter; Marshall, Paul; Troe, Juergen

    2015-01-01

    Experimental data for the unimolecular decomposition of CS2 from the literature are analyzed by unimolecular rate theory with the goal of obtaining rate constants for the reverse reaction S + CS (+M) -> CS2 (+M) over wide temperature and pressure ranges. The results constitute an important input...

  14. CoVaCS: a consensus variant calling system.

    Science.gov (United States)

    Chiara, Matteo; Gioiosa, Silvia; Chillemi, Giovanni; D'Antonio, Mattia; Flati, Tiziano; Picardi, Ernesto; Zambelli, Federico; Horner, David Stephen; Pesole, Graziano; Castrignanò, Tiziana

    2018-02-05

    The advent and ongoing development of next generation sequencing technologies (NGS) has led to a rapid increase in the rate of human genome re-sequencing data, paving the way for personalized genomics and precision medicine. The body of genome resequencing data is progressively increasing underlining the need for accurate and time-effective bioinformatics systems for genotyping - a crucial prerequisite for identification of candidate causal mutations in diagnostic screens. Here we present CoVaCS, a fully automated, highly accurate system with a web based graphical interface for genotyping and variant annotation. Extensive tests on a gold standard benchmark data-set -the NA12878 Illumina platinum genome- confirm that call-sets based on our consensus strategy are completely in line with those attained by similar command line based approaches, and far more accurate than call-sets from any individual tool. Importantly our system exhibits better sensitivity and higher specificity than equivalent commercial software. CoVaCS offers optimized pipelines integrating state of the art tools for variant calling and annotation for whole genome sequencing (WGS), whole-exome sequencing (WES) and target-gene sequencing (TGS) data. The system is currently hosted at Cineca, and offers the speed of a HPC computing facility, a crucial consideration when large numbers of samples must be analysed. Importantly, all the analyses are performed automatically allowing high reproducibility of the results. As such, we believe that CoVaCS can be a valuable tool for the analysis of human genome resequencing studies. CoVaCS is available at: https://bioinformatics.cineca.it/covacs .

  15. Vertical profile of 137Cs in soil.

    Science.gov (United States)

    Krstić, D; Nikezić, D; Stevanović, N; Jelić, M

    2004-12-01

    In this paper, a vertical distribution of 137Cs in undisturbed soil was investigated experimentally and theoretically. Soil samples were taken from the surroundings of the city of Kragujevac in central Serbia during spring-summer of 2001. The sampling locations were chosen in such a way that the influence of soil characteristics on depth distribution of 137Cs in soil could be investigated. Activity of 137Cs in soil samples was measured using a HpGe detector and multi-channel analyzer. Based on vertical distribution of 137Cs in soil which was measured for each of 10 locations, the diffusion coefficient of 137Cs in soil was determined. In the next half-century, 137Cs will remain as the source of the exposure. Fifteen years after the Chernobyl accident, and more than 30 years after nuclear probes, the largest activity of 137Cs is still within 10 cm of the upper layer of the soil. This result confirms that the penetration of 137Cs in soil is a very slow process. Experimental results were compared with two different Green functions and no major differences were found between them. While both functions fit experimental data well in the upper layer of soil, the fitting is not so good in deeper layers. Although the curves obtained by these two functions are very close to each other, there are some differences in the values of parameters acquired by them.

  16. 137Cs concentration in some Philippine foods

    International Nuclear Information System (INIS)

    dela Cruz, B.; Marzan, A.M.; Lagmay, N.; Anden, A.

    1977-01-01

    The current investigation being made by the Philippine Atomic Research Center on the 137 Cs content of the different foods commonly used by the Filipinos is described and preliminary results are reported. The 137 Cs content is determined radiochemically only for the edible portion of the food

  17. {sup 137}Cs in northern Adriatic sediments

    Energy Technology Data Exchange (ETDEWEB)

    Barisic, D; Lulic, S; Vdovic, N; Vertacnik, A [Center for Marine Research - Department Zagreb, ' Ruder Boskovic' Institute, Zagreb (Croatia); Juracic, M [Department of Geology, Faculty of Natural Sciences, University of Zagreb, Zagreb (Croatia)

    1996-01-01

    The activity of {sup 137}Cs in shallow northern Adriatic sediments was obtained on the basis of measurement results from 25 sediment box cores, sampled during the Adriatic Scientific COoperation Program (ASCOP) 16 cruise in the summer 1990. {sup 137}Cs was determined in surface sediments (0-3 cm) and 12-15 cm-deep sediment. It was found that the lowest caesium concentrations correspond to sands, which are spread along the Croatian coast. Parallel to the Italian coast, {sup 137}Cs concentrations in pelites are the highest. It seems that the influence of Po River is significant for {sup 137}Cs activities in recent marine sediments along Italian coast south of Po River delta. Significantly higher {sup 137}Cs activities in 0-3 cm sediment layer can be attributed to the deposition caused by Chernobyl accident. (author)

  18. 137Cs in northern Adriatic sediments

    International Nuclear Information System (INIS)

    Barisic, D.; Lulic, S.; Vdovic, N.; Vertacnik, A.; Juracic, M.

    1996-01-01

    The activity of 137 Cs in shallow northern Adriatic sediments was obtained on the basis of measurement results from 25 sediment box cores, sampled during the Adriatic Scientific COoperation Program (ASCOP) 16 cruise in the summer 1990. 137 Cs was determined in surface sediments (0-3 cm) and 12-15 cm-deep sediment. It was found that the lowest caesium concentrations correspond to sands, which are spread along the Croatian coast. Parallel to the Italian coast, 137 Cs concentrations in pelites are the highest. It seems that the influence of Po River is significant for 137 Cs activities in recent marine sediments along Italian coast south of Po River delta. Significantly higher 137 Cs activities in 0-3 cm sediment layer can be attributed to the deposition caused by Chernobyl accident. (author)

  19. Biokinetic model for 137 Cs

    International Nuclear Information System (INIS)

    Melo, Dunstana Rabelo de

    1995-01-01

    The main objective of this work was to provide a realistic biokinetic model for 137 Cs metabolism. This model was based on the retention of cesium in 57 people contaminated in the Goiania accident, ages 1 to 73 y old, complemented by data obtained in an experiment with beagle dogs, and data taken from the open literature. Cesium is distributed among all tissues and organs of the body. Its main retention site is the skeletal muscle tissue. Mathematically, cesium retention in the body may be described by a sum of three terms exponential equation. The first term represents the fraction which is rapidly eliminated in urine. This fraction is weight dependent (negative correlation). The second term represents the retention of cesium in tissues and organs of the body. For children and adolescents, the second term biological half-life is a function of the weight. For adults, it is correlated with sex. Men present a higher retention of cesium than women. The third term correspond to a retention fraction of the order of 0,1% of the initial body burden. It is characterized by a very long half-life and represents a subcellular retention of cesium in the skeletal muscle tissue. During pregnancy the transfer factor from the mother to the fetus is correlated to the amount of cesium in the blood and it is equal to 1, if the intake of cesium occurs pregnancy. (author)

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

    International Nuclear Information System (INIS)

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

    2013-01-01

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

  1. A novel vanadosilicate with hexadeca-coordinated Cs+ ions as a highly effective Cs+ remover

    International Nuclear Information System (INIS)

    Datta, Shuvo Jit; Moon, Won Kyung; Choi, Do Young; Hwang, In Chul; Yoon, Kyung Byung

    2014-01-01

    The effective removal of 137 Cs + ions from contaminated groundwater and seawater and from radioactive nuclear waste solutions is crucial for public health and for the continuous operation of nuclear power plants. Various 137 Cs + removers have been developed, but more effective 137 Cs + removers are still needed. A novel microporous vanadosilicate with mixed-valence vanadium (V 4+ and V 5+ ) ions is now reported, which shows an excellent ability for Cs + capture and immobilization from groundwater, seawater, and nuclear waste solutions. This material is superior to other known materials in terms of selectivity, capacity, and kinetics, and at very low Cs + concentrations, it was found to be the most effective material for the removal of radioactive Cs + ions under the test conditions. This novel vanadosilicate also contains hexadeca-coordinated Cs + ions, which corresponds to the highest coordination number ever described.

  2. Molecular CsF{sub 5} and CsF{sub 2}{sup +}

    Energy Technology Data Exchange (ETDEWEB)

    Rogachev, Andrey Yu. [Illinois Institute of Technology, IL (United States). Dept. of Biological and Chemical Sciences; Miao, Mao-sheng [California State Univ., Northridge, CA (United States). Dept. of Chemistry and Biochemistry; Beijing Computational Science Research Center (China); Merino, Gabriel [Centro de Investigacion y de Estudios Avanzados, Unidad Merida (Mexico). Dept. de Fisica Aplicada; Hoffmann, Roald [Cornell Univ., Ithaca, NY (United States). Dept. of Chemistry and Chemical Biology

    2015-07-06

    D{sub 5h} star-like CsF{sub 5}, formally isoelectronic with known XeF{sub 5}{sup -} ion, is computed to be a local minimum on the potential energy surface of CsF{sub 5}, surrounded by reasonably large activation energies for its exothermic decomposition to CsF + 2F{sub 2}, or to CsF{sub 3} (three isomeric forms) + F{sub 2}, or for rearrangement to a significantly more stable isomer, a classical Cs{sup +} complex of F{sub 5}{sup -}. Similarly the CsF{sub 2}{sup +} ion is computed to be metastable in two isomeric forms. In the more symmetrical structures of these molecules there is definite involvement in bonding of the formally core 5p levels of Cs.

  3. Sorption Characteristics of 137Cs and 90Sr into Rembang and Sumedang Soils

    Directory of Open Access Journals (Sweden)

    Budi Setiawan

    2016-12-01

    Full Text Available In order to understand the sorption behavior of 137Cs and 90Sr into soil sample from Rembang and Subang, it is important to estimate the effect of contact time, ionic strength and concentration of metal ion in the solution. For this reason, the interaction of 137Cs and 90Sr with soil sample has been examined. The study performed at trace concentration (~10-8 M of CsCl and SrCl2, and batch method was used. NaCl has been selected as a representative of the ionic strength with 0.1; 0.5 and 1.0 M concentrations. Concentration of 10-8~10-4 M CsCl and SrCl2 were used for study the effect of Cs and Sr concentrations in solution. Apparent distribution coefficient was used to predict the sorption behavior. The sorption equilibrium of 137Cs and 90Sr into soil was attained after 5 days contacted with Kd value around 3300-4200 mL/g, where Kd was defined as the ratio of number of radionuclide activity absorbed in solid phase per-unit mass to the number of radionuclide activity remains is solution per-unit volume. Presence of NaCl as background salt in the solution affected Kd values due to competition among metal ions into soil samples. Increase of Cs or Sr concentration in solution made Kd value decreased drastically. This information is expected could provide an important input for the planning and design of radioactive waste disposal system in Java Island in the future.

  4. Transfer of 137Cs to wild vegetables

    International Nuclear Information System (INIS)

    Ito, Nobuhiko; Natsuhori, Masahiro; Mezawa, Akane; Kawakami, Akira

    1998-01-01

    For the evaluation of internal radiation dose, it is needed to estimate the amount of radionuclide incorporated to human body using a simulation model. 137 Cesium (Cs) is easily transferred associating with food intake as well as potassium and so, Cs is an important nuclide for evaluation of internal radiation. 137 Cs concentrations in wild vegetables are higher than those of cultured vegetables and milk. Therefore, the transfer coefficients of 137 Cs from soil to wild vegetables were estimated in this study. Wild vegetables and soils of their farms were collected in the Hakkoda Mountain range of Aomori Prefecture. The levels of 137 Cs in wild vegetables were 0.42-18.35 (Bq/kg), whereas those in cabbage and spinach were 0.08 and 0.01 (Bq/kg), respectively, indicating that the Cs level is dozens to several hundreds times higher in wild vegetables than cultured ones. And the transfer coefficient was estimated as 0.003-0.94 for the former and 0.001-0.8 for the latter. On the other hand, 1 37 Cs levels of the soils on which wild vegetables grew was 28.0 Bq/kg and it was 3.9 Bq/kg for the farm soil. Furthermore, the effects of water content and pH of the soil on the transfer coefficient were studied. (M.N.)

  5. Potential value of Cs-137 capsules

    Energy Technology Data Exchange (ETDEWEB)

    Bloomster, C.H.; Brown, D.R.; Bruno, G.A.; Hazelton, R.F.; Hendrickson, P.L.; Lezberg, A.J.; Tingey, G.L.; Wilfert, G.L.

    1985-04-01

    We determined the value of Cs-137 compared to Co-60 as a source for the irradiation of fruit (apples and cherries), pork and medical supplies. Cs-137, in the WESF capsule form, had a value of approximately $0.40/Ci as a substitute for Co-60 priced at approximately $1.00/Ci. The comparison was based on the available curies emitted from the surface of each capsule. We developed preliminary designs for fourteen irradiation facilities; seven were based on Co-60 and seven were based on Cs-137. These designs provided the basis for estimating capital and operating costs which, in turn, provided the basis for determining the value of Cs-137 relative to Co-60 in these applications. We evaluated the effect of the size of the irradiation facility on the value of Cs-137. The cost of irradiation is low compared to the value of the product. Irradiation of apples for disinfestation costs $.01 to .02 per pound. Irradiation for trichina-safe pork costs $.02 per pound. Irradiation of medical supplies for sterilization costs $.07 to .12 per pound. The cost of the irradiation source, either Co-60 or Cs-137, contributed only a minor amount to the total cost of irradiation, about 5% for the fruit and hog cases and about 20% for the medical supply cases. We analyzed the sensitivity of the irradiation costs and Cs-137 value to several key assumptions.

  6. Potential value of Cs-137 capsules

    International Nuclear Information System (INIS)

    Bloomster, C.H.; Brown, D.R.; Bruno, G.A.; Hazelton, R.F.; Hendrickson, P.L.; Lezberg, A.J.; Tingey, G.L.; Wilfert, G.L.

    1985-04-01

    We determined the value of Cs-137 compared to Co-60 as a source for the irradiation of fruit (apples and cherries), pork and medical supplies. Cs-137, in the WESF capsule form, had a value of approximately $0.40/Ci as a substitute for Co-60 priced at approximately $1.00/Ci. The comparison was based on the available curies emitted from the surface of each capsule. We developed preliminary designs for fourteen irradiation facilities; seven were based on Co-60 and seven were based on Cs-137. These designs provided the basis for estimating capital and operating costs which, in turn, provided the basis for determining the value of Cs-137 relative to Co-60 in these applications. We evaluated the effect of the size of the irradiation facility on the value of Cs-137. The cost of irradiation is low compared to the value of the product. Irradiation of apples for disinfestation costs $.01 to .02 per pound. Irradiation for trichina-safe pork costs $.02 per pound. Irradiation of medical supplies for sterilization costs $.07 to .12 per pound. The cost of the irradiation source, either Co-60 or Cs-137, contributed only a minor amount to the total cost of irradiation, about 5% for the fruit and hog cases and about 20% for the medical supply cases. We analyzed the sensitivity of the irradiation costs and Cs-137 value to several key assumptions

  7. Performance of a high-resolution CsI(Tl)-PIN readout detector

    International Nuclear Information System (INIS)

    Kudenko, Yu.G.; Imazato, J.

    1992-10-01

    A study of a large-volume CsI(Tl) detector with a PIN diode readout was carried out. Our results show a light output of ≤20000 photoelectrons/MeV, an equivalent noise charge (rms) of about 900 electrons, and an equivalent noise level of ≤ 60 keV. We obtained an energy resolution of 11.2% (fwhm) for 1275 keV gamma rays from a 22 Na source. The characteristics of the PIN - preamplifier system as well as the parameters of a small CsI(Tl) - PIN detector with a direct and wavelength shifter readout are also reported. (author)

  8. Anisotropy in diffusion and activation energies of I- and CS+ ions in compacted smectite

    International Nuclear Information System (INIS)

    Haruo Sato

    2005-01-01

    The anisotropies and the effect of salinity in the apparent diffusivities (D a ) and activation energies (ΔE a ) of I - and Cs + in compacted Na-smectite were studied. The diffusion experiments in the parallel and perpendicular directions to the orientated direction of smectite particles were performed as a function of smectite's dry density (0.9-1.4 Mg/m 3 ), salinity ([NaCl]=0.01, 0.51 M) and temperature (295-333 K). The Da-values for both ions tended to be higher in the parallel direction than in the perpendicular direction to the orientated direction of smectite particles. The Da-values of I - in the parallel direction decreased with increasing salinity only at low-dry density, but those of Cs + increased with increasing salinity in all conditions. Considering electrostatic effect from the surface of smectite aggregates and the change in tortuosity on dry density, salinity and diffusion direction, I - is interpreted to mainly diffuse in interstitial pores. While, Cs + can diffuse in both interlayer and interstitial pores, and the Da-values of Cs + are presumed to have elevated by the decrease in retardation by competition with Na + . The ΔE a -values of I - , similar levels (ΔE a =15.1-16.1 kJ/mol) to that of the ionic diffusivity in free water (Do) for I - (ΔE a =17.36 kJ/mol) at low-dry density, increased with increasing dry density. On the contrary, the ΔE a -values of Cs + , clearly higher (ΔE a =23.7-25.7 kJ/mol) than that of the Do for Cs + (ΔE a =16.47 kJ/mol) even at low-dry density, increased with increasing dry density. Such high ΔE a -values for Cs + can be explained by considering the ion exchange enthalpy between Cs + and Na + in smectite (ΔH 0 = -11.1 kJ/mol) at low-dry density, and are considered to be due to the effects of the decrease in the activity of porewater and ΔH 0 at high-dry density. (authors)

  9. 137Cs distribution in guava trees

    International Nuclear Information System (INIS)

    Mosquera, B.; Veiga, R.; Mangia, L.; Carvalho, C.; Estellita, L.; Uzeda, D.; Facure, A.; Violini, B.; Anjos, R.M.

    2004-01-01

    This paper presents results of 137 Cs concentration measured from a guava tree cultivated after the first decontamination work of one of the sites where the worst Brazilian radiological accident occurred. The present work aims to verify how the 137 Cs is transported and distributed along the tropical trees. Bi-dimensional analyses of the radial distribution of 137 Cs in the main trunk are also presented. Neither symmetrical nor homogeneous behaviors of the specific activity distribution in the tree rings were observed. (author)

  10. {sup 137}Cs distribution in guava trees

    Energy Technology Data Exchange (ETDEWEB)

    Mosquera, B.; Veiga, R.; Mangia, L.; Carvalho, C.; Estellita, L.; Uzeda, D.; Facure, A.; Violini, B.; Anjos, R.M. [Universidade Federal Fluminense, Niteroi, RJ (Brazil). Inst. de Fisica

    2004-09-15

    This paper presents results of {sup 137}Cs concentration measured from a guava tree cultivated after the first decontamination work of one of the sites where the worst Brazilian radiological accident occurred. The present work aims to verify how the {sup 137}Cs is transported and distributed along the tropical trees. Bi-dimensional analyses of the radial distribution of {sup 137}Cs in the main trunk are also presented. Neither symmetrical nor homogeneous behaviors of the specific activity distribution in the tree rings were observed. (author)

  11. CsI and some new photocathodes

    International Nuclear Information System (INIS)

    Anderson, D.F.; Kwan, S.; Peskov, V.

    1993-06-01

    A discussion of the possible sources of discrepancies in the measurements of the quantum efficiency of CsI photocathodes is presented. We propose that the major causes for disagreements in QE are due to the QE dependence on the current density extracted from the photocathode, on the electric field, and on the temperature of the photocathode. Preliminary results on TMAE enhanced GaAs and Si, plus TMAE protected CsTe and SbCs photocathodes, operated in gas, are also presented

  12. Coordination polyhedra CsCln in crystals

    International Nuclear Information System (INIS)

    Serezhkin, V.N.; Serezhkina, L.B.

    1999-01-01

    Characteristics of the Voronoi-Dirichlet polyhedrons are estimated for 133 crystallographic cesium atoms in chlorides Cs x M y Cl z (M=Cd, Sc, V, Nb, Mo, W, Ru, Re, etc.). It is found that cesium atoms have coordination numbers 6,8,9,10, 11 and 12 as regards the chlorine atoms. The results of cesium atom coordination sphere examination by the crossing spheres method are presented. Metal-metal interactions (including Cs-Cs) in the structure of certain chlorides are revealed

  13. Regeneration of Used Frying Palm Oil with Coffee Silverskin (CS), CS Ash (CSA) and Nanoparticles of CS (NCS).

    Science.gov (United States)

    Ismail, Samir Abd-Elmonem A; El-Anany, Ayman Mohammed; Ali, Rehab Farouk M

    2017-01-01

    The present investigation aimed to evaluate the efficiency of coffee silverskin (CS), CS ash (CSA) and nanoparticles of CS (NCS) in regeneration the quality of used frying palm oil. The adsorbents were mixed individually with used frying palm oil at level 4% (w/v) for 60 min. The properties of CS, CSA and NCS adsorbents were studied using (SEM) scanning electron microscopy technique. Some of physico-chemical characteristics of used frying palm oil (UFPO) and UFPO treated with adsorbents were determined. The results showed that the CS ash particles composed of irregular spherical and semispherical grains with deep cavities. The size of particles of CS ash ranged in diameter from 1.1 to 1.7 µm. The morphology of NCS consisted of cluster-type spherical nanoparticles and flakes. The particle size of NCS varies from 0.9 to 1.7 µm. Purification treatments caused marked (poil compared to untreated oil. The treatment of UFPO with 4% of adsorbents caused significant reductions in the content of free fatty acids ranged from 51.2 to 65.0%. The lowest level of peroxide (2.1 meq/kg) was recorded for UFPO treated with 4% of NCS. The highest reductions (72.8; 70.0%) in p-anisidine value were observed in UFPO treated with 4% of CSA and NCS, respectively. Treatment of UFPO with 4% of CS, CSA and NCS significantly lowered the polar content from 13.9% to 6.3, 4.8 and 3.9%, respectively. The results also indicate that CSA and NCS have nearly the same adsorption efficiency in lowering polymer content of UFPO. Filtration treatment of UFPO with 4% of CS, CSA and NCS markedly lowered the viscosity and colour values of treated UFPO.

  14. [Energy pooling collisions for K(4P) + Cs(5D) in a K-Cs mixture].

    Science.gov (United States)

    Aihemaiti, Pulati; Dai, Kang; Lu, Xin-hong; Shen, Yi-fan

    2005-04-01

    The rate coefficients for energy-pooling collisions K(4P) + Cs(5D) --> Cs(6S) + K(4D, 6S) in the K-Cs vapor mixture were measured relative to a known energy-pooling rate coefficient of a homonuclear reaction [i. e., Cs(6P) + Cs(5D) --> Cs(6S) + Cs (7D(J))]. Populations of the Cs(6P, 5D) and K(4P) states were produced by photodissociation of K2 and Cs2 molecules through the use of a dye laser radiation. The resulting fluorescence included the direct components emitted in the decay of the excited states produced by photodissociation and the induced components arising from the collisionally populated states. By combining relative intensities of the components with the effective lifetimes of Cs(6P) and K(4P) states, the rate coefficients (in units of 10(-9) cm3 x s(-1)) for the heteronuclear energy-pooling were found to be 2.6 and 3.6, respectively. The contribution to the rate coefficients from other processes are discussed.

  15. Properties of Cs-intercalated single wall carbon nanotubes investigated by 133Cs Nuclear Magnetic resonance

    KAUST Repository

    Schmid, Marc R.

    2012-11-01

    In the present study, we investigated Cs-intercalated single wall carbon nanotubes (SWCNTs) using 133Cs Nuclear Magnetic resonance. We show that there are two types of Cs cations depending on the insertion level. Indeed, at low concentrations, Static spectra analysis shows that the Cs (α)+ species are fully ionized, i.e. α equal ca.1, while at higher concentrations a second paramagnetically shifted line appears, indicating the formation of Cs (β)+ ions with β < α ∼ +1. At low concentrations and low temperatures the Cs (α)+ ions exhibit a weak hyperfine coupling to the SWCNT conduction electrons, whereas, at higher temperatures, a thermally activated slow-motion diffusion process of the Cs (α)+ ions occurs along the interstitial channels present within the carbon nanotube bundles. At high concentrations, the Cs (β)+ ions seem to occupy well defined positions relative to the carbon lattice. As a matter of fact, the Korringa relaxation behavior suggests a strong hyperfine coupling between Cs nuclei and conduction electrons in the carbon nanotubes and a partial charge transfer, which suggest a plausible Cs(6s)-C(2p) hybridization. © 2012 Elsevier Ltd. All rights reserved.

  16. 135Cs activity and 135Cs/137Cs atom ratio in environmental samples before and after the Fukushima Daiichi Nuclear Power Plant accident.

    Science.gov (United States)

    Yang, Guosheng; Tazoe, Hirofumi; Yamada, Masatoshi

    2016-04-07

    (135)Cs/(137)Cs is a potential tracer for radiocesium source identification. However, due to the challenge to measure (135)Cs, there were no (135)Cs data available for Japanese environmental samples before the Fukushima Daiichi Nuclear Power Plant (FDNPP) accident. It was only 3 years after the accident that limited (135)Cs values could be measured in heavily contaminated environmental samples. In the present study, activities of (134)Cs, (135)Cs, and (137)Cs, along with their ratios in 67 soil and plant samples heavily and lightly contaminated by the FDNPP accident were measured by combining γ spectrometry with ICP-MS/MS. The arithmetic means of the (134)Cs/(137)Cs activity ratio (1.033 ± 0.006) and (135)Cs/(137)Cs atom ratio (0.334 ± 0.005) (decay corrected to March 11, 2011), from old leaves of plants collected immediately after the FDNPP accident, were confirmed to represent the FDNPP derived radiocesium signature. Subsequently, for the first time, trace (135)Cs amounts before the FDNPP accident were deduced according to the contribution of global and FDNPP accident-derived fallout. Apart from two soil samples with a tiny global fallout contribution, contributions of global fallout radiocesium in other soil samples were observed to be 0.338%-52.6%. The obtained (135)Cs/(137)Cs database will be useful for its application as a geochemical tracer in the future.

  17. New technology of CRDM-CS

    International Nuclear Information System (INIS)

    Yasushi Nozaki; Hiroyuki Ukon; Toshiaki Matsumura; Yoshihiro Sakurai; Sigenori Hatazawa; Hitoshi Yamagishi; Katsuji Kaneizumi; Hisashi Yasuda

    2005-01-01

    Control Rod Drive Mechanism Control System (CRDM-CS) for PWR Nuclear Power Plant was developed as a domestic product in 1975 and it has been applied to the commercial power plants. Since then, the CRDM-CS has been continuously improved through applying a double-hold-system, an intensified monitoring system, etc. As the result of these modifications unexpected rod drops have never occurred more than ten years in Japanese PWR plants. The system is still so high reliable, however, the technologies of employed devices are old-fashioned and we face on the difficulty to keep spare-parts these days. On the other hand, there are new movements to seek after the plant life extension of 60 years. These situations require a modernized CRDM-CS to accomplish the reliability in accordance to the plant life extension. to comply the above-mentioned object we developed a new CRDM-CS applied with following technologies; 1) Digitalized logic cabinet, 2) I.G.B.T in the main circuit of power cabinet, 3) Standardized cabinet by employing the unit structure, 4) Unnecessary DC hold power cabinet. These measures can play an important role in cost cutting and space reduction in replacing CRDM-CS. The concepts in developing the new CRDM-CS, the applied technologies to the power cabinet, the system structure and characteristics of the logic cabinet and the outline of verification test and result are discussed in this paper. (authors)

  18. Fast CsI-phoswich detector

    International Nuclear Information System (INIS)

    Langenbrunner, J.R.

    1996-01-01

    An improved phoswich radiation detector used pure CsI crystal and a fast plastic scintillator and a single photomultiplier tube. The plastic is arranged to receive incident radiation, and that which passed through then strikes the CsI crystal. Scintillation light from both the plastic and CsI crystal are applied to the photomultiplier tube, with the light from the plastic passing through the crystal without absorption therein. Electronics are provided for analyzing the output of the photomultiplier tube to discriminate responses due to the plastic and the CsI crystal, through short gate and long gate integration, to produce results which are indicative of the characteristics of the different types of incident radiation, even in the presence of large amounts of radiation. The phoswich detector has excellent timing resolution. The scintillators of the CsI- phoswich were chosen for their fast risetimes, of about 3 ns for NE102A, and 30 ns for the pure CsI. 5 figs

  19. 137Cs metabolism in pregnant women

    International Nuclear Information System (INIS)

    Melo, D.R.; Lipsztein, J.L.; Oliveira, C.A.N.; Bertelli, L.

    2000-01-01

    Data from two pregnant women contaminated with 137 Cs, body burdens of 0.2 and 300 MBq, respectively at the time of the Goiania accident, were compared. The first one, with lower body burden was exposed during the fourth month of pregnancy, while the second became pregnant three years and eight months after 137 Cs intake. For the first woman 137 Cs concentrations were equal for the mother, infant and placenta, indicating an easy and homogeneous transport of 137 Cs from mother to foetus. The whole body monitoring data from the second woman, who became pregnant four years after intake, did not show a reduction in biological half-life during the pregnancy. Cs concentration in the mother was found to be 13 times higher than in the infant. One possible reason for this result is that four years after intake, Cs is supposed to be concentrated mainly in skeletal muscle tissue. During the pregnancy the blood flux becomes higher in most of the organs and tissues except brain, liver and skeletal muscle tissue. (author)

  20. Concentration of 134Cs and 137Cs in Malaysian palm products

    International Nuclear Information System (INIS)

    Yii Mei Wo; Nor Aza Hassan; Narizan Sanusi

    2008-08-01

    Until today, countries importing food products from Malaysia, in region such as Indian Continental, Middle East, Central Europe and Central America still require the products to be tested for the radioactive contamination particularly for 134 Cs and 137 Cs. Information extracted from 3371 analytical results observed on isotopic concentration for 134 Cs and 137 Cs in the exported Malaysia origins palm products between years 2002 until 2007 had been summarized and reported in this work. Data shown that the concentration level of the concerned radio nuclides are below the minimum detectable activity and also well below maximum permissible limits adopted by Malaysian Government and also the international bodies. (Author)

  1. Prediction of Intrinsic Cesium Desorption from Na-Smectite in Mixed Cation Solutions.

    Science.gov (United States)

    Fukushi, Keisuke; Fukiage, Tomo

    2015-09-01

    Quantitative understanding of the stability of sorbed radionuclides in smectite is necessary to assess the performance of engineering barriers used for nuclear waste disposal. Our previous study demonstrated that the spatial organization of the smectite platelets triggered by the divalent cations led to the apparent fixation of intrinsic Cs in smectite, because some Cs is retained inside the formed tactoids. Natural water is usually a mixture of Na(+) and divalent cations (Ca(2+) and Mg(2+)). This study therefore investigated the desorption behavior of intrinsic Cs in Na-smecite in mixed Na(+)-divalent cation solutions under widely various cation concentrations using batch experiments, grain size measurements, and cation exchange modeling (CEM). Results show that increased Na(+) concentrations facilitate Cs desorption because Na(+) serves as the dispersion agent. A linear relation was obtained between the logarithm of the Na(+) fraction and the accessible Cs fraction in smectite. That relation enables the prediction of accessible Cs fraction as a function of solution cationic compositions. The corrected CEM considering the effects of the spatial organization suggests that the stability of intrinsic Cs in the smectite is governed by the Na(+) concentration, and suggests that it is almost independent of the concentrations of divalent cations in natural water.

  2. Cs[FeSe{sub 2}], Cs{sub 3}[FeSe{sub 2}]{sub 2}, and Cs{sub 7}[Fe{sub 4}Se{sub 8}]. Missing links of known chalcogenido ferrate series

    Energy Technology Data Exchange (ETDEWEB)

    Stueble, Pirmin; Roehr, Caroline [Institut fuer Anorganische und Analytische Chemie, Universitaet Freiburg (Germany)

    2017-11-17

    The three cesium selenido ferrate title compounds with an Se:Fe ratio of 2:1 were synthesized from stoichiometric samples reacting elemental Cs either (A) with Fe and Se in a double-crucible setup (Cs[FeSe{sub 2}], Cs{sub 3}[FeSe{sub 2}]{sub 2}) or (B) with previously prepared FeSe{sub 2} (Cs{sub 3}[FeSe{sub 2}]{sub 2}, Cs{sub 7}[Fe{sub 4}S{sub 8}]) (T{sub max} = 800-1000 C). The pure Fe{sup III} ferrate Cs[FeSe{sub 2}] crystallizes in the Tl[FeSe{sub 2}] type [monoclinic, space group C2/m, a = 1392.95(10), b = 564.43(3), c = 737.44(6) pm, β = 119.163(5) , Z = 4, R{sub 1} = 0.0550]. It is thus not isotypic to all other alkali ferrates(III) A[FeS{sub 2}] and A[FeSe{sub 2}] containing chains of edge-sharing tetrahedra, but crystallizes in a t2 subgroup of the Immm structure of Cs[FeS{sub 2}]. The mixed-valent chain compound Cs{sub 3}[FeSe{sub 2}]{sub 2} is isotypic to its sulfido analogue [orthorhombic, space group Pnma, a = 777.88(6), b = 1151.02(6), c = 1341.61(7) pm, Z = 4, R{sub 1} = 0.0470]. In contrast to the isopunctal Na{sub 3}[FeSe{sub 2}]{sub 2} type K/Rb compounds the chains are only slightly corrugated. The monoclinic, likewise mixed-valent Fe{sup II/III} selenido ferrate Cs{sub 7}[Fe{sub 4}Se{sub 8}] [monoclinic, space group C2/c, a = 1953.79(10), b = 879.71(5), c = 1717.03(10) pm, β = 117.890(2) , Z = 4, R{sub 1} = 0.0816] is isostructural both to the cesium sulfido and tellurido compound. The structure contains oligomeric moieties of four edge sharing [FeSe{sub 4}] tetrahedra forming slightly distorted tetrahedral clusters [Fe{sub 4}Se{sub 8}]{sup 7-}, which are surrounded by a cube of 26 Cs cations. Based on a structure map, the crystal chemistry of the three title compounds is discussed together with all chain/cluster ferrates of the general series A{sub 1+x}[Fe{sup III}{sub 1-x}Fe{sup II}{sub x}Q{sub 2}] (x = 0-1; A = Na, K, Rb, Cs; Q = S, Se, Te). (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  3. Dynamic moments of inertia in Xe, Cs and Ba nuclei

    International Nuclear Information System (INIS)

    El-Samman, H.; Barci, V.; Gizon, A.

    1984-01-01

    The γ-rays following the reactions induced by 12 C ions on 115 In, 112 , 117 , 122 Sn and 123 Sb targets have been investigated using six NaI(Tl) detectors in a two-dimensional arrangement. The collective moment of inertia I( 2 ) /sub band/ of 118 , 122 Xe, 123 Cs and 128 , 130 Ba have been extracted from the energy-correlation spectra. The behaviour of these nuclei and the observed differences are interpreted in terms of high-spin collective properties. Data are also presented on the effective moment of inertia I( 2 )/sub eff/ of 118 Xe and 130 Ba measured by sum-spectrometer techniques. 13 references

  4. Decay of 132Cs and nuclear structure of 132Xe

    International Nuclear Information System (INIS)

    Cruz, M.T.F. da; Goldman, I.D.

    1989-02-01

    Gamma spectroscopy, coincidence and angular correlation experiments were performed, in an extensive study of 132 Cs decay. The population intensities of states in 132 Ba were measured, some upper limits were determined and the value of the transition to the 4 1 + state of 132 Ba has drastically changed. A new gamma transition of 688 KeV was detected and located in the level scheme of 132 Xe. The angular correlation measurements were performed with a Ge(Li)-NaI(Tl) spectrometer and helped in choosing the spin value for the 1804 KeV state of 132 Xe. Kumar-Baranger-type calculations were performed for the 132 Xe fairly good results. The resulting potential energy surface for 132 Xe is very different from that of Gneuss and Greiner model, suggesting the need for any quadrupole moment measurement for this nucleus. (author) [pt

  5. Geographical trends in 137Cs fallout from the Chernobyl accident and leaching from natural surface soil in Norway

    International Nuclear Information System (INIS)

    Gjelsvik, Runhild; Steinnes, Eiliv

    2013-01-01

    In order to follow the turnover of 137 Cs in natural soils and estimate future trends in exposure of livestock, samples of natural surface soils were collected at 0–3 cm depth at 464 sites in 1995 and 463 sites in 2005 covering the country. In both cases the geographical pattern observed was similar to the original distribution from 1986, but the decline of 137 Cs activity in the surface soil was not the same everywhere. In 1995 the 137 Cs reduction since 1986 was found to be considerably greater in coastal areas than farther inland. The main reason for this appears to be the much greater deposition of marine cations such as Mg 2+ and Na + in the coastal areas, replacing Cs ions fixed on soil particle surfaces. This cation exchange appeared to be particularly strong near the southern coast where deposition of NH 4 + from transboundary air pollution is evident in addition to the marine cations. During 1995–2005 the 137 Cs decline in the surface soil was more uniform over the country than in the preceding 10-year period but still significantly higher in coastal areas than inland. Differences in precipitation chemistry may have influenced the uptake of 137 Cs in terrestrial food chains. -- Highlights: • We investigated the decline of 137 Cs in natural surface soil in Norway in 1986–2005. • The reduction of 137 Cs in soil was greater in coastal areas then farther inland. • Deposition of marine cations were replacing Cs ions fixed on soil particle surfaces. • In areas with nitrogen compounds NH 4 + cation may compete with Cs + cation

  6. VERA-CS Verification & Validation Plan

    Energy Technology Data Exchange (ETDEWEB)

    Downar, Thomas [Univ. of Michigan, Ann Arbor, MI (United States)

    2017-02-01

    This report summarizes the current status of VERA-CS Verification and Validation for PWR Core Follow operation and proposes a multi-phase plan for continuing VERA-CS V&V in FY17 and FY18. The proposed plan recognizes the hierarchical nature of a multi-physics code system such as VERA-CS and the importance of first achieving an acceptable level of V&V on each of the single physics codes before focusing on the V&V of the coupled physics solution. The report summarizes the V&V of each of the single physics codes systems currently used for core follow analysis (ie MPACT, CTF, Multigroup Cross Section Generation, and BISON / Fuel Temperature Tables) and proposes specific actions to achieve a uniformly acceptable level of V&V in FY17. The report also recognizes the ongoing development of other codes important for PWR Core Follow (e.g. TIAMAT, MAMBA3D) and proposes Phase II (FY18) VERA-CS V&V activities in which those codes will also reach an acceptable level of V&V. The report then summarizes the current status of VERA-CS multi-physics V&V for PWR Core Follow and the ongoing PWR Core Follow V&V activities for FY17. An automated procedure and output data format is proposed for standardizing the output for core follow calculations and automatically generating tables and figures for the VERA-CS Latex file. A set of acceptance metrics is also proposed for the evaluation and assessment of core follow results that would be used within the script to automatically flag any results which require further analysis or more detailed explanation prior to being added to the VERA-CS validation base. After the Automation Scripts have been completed and tested using BEAVRS, the VERA-CS plan proposes the Watts Bar cycle depletion cases should be performed with the new cross section library and be included in the first draft of the new VERA-CS manual for release at the end of PoR15. Also, within the constraints imposed by the proprietary nature of plant data, as many as possible of the FY17

  7. Relative injectivity and CS-modules

    Directory of Open Access Journals (Sweden)

    Mahmoud Ahmed Kamal

    1994-01-01

    Full Text Available In this paper we show that a direct decomposition of modules M⊕N, with N homologically independent to the injective hull of M, is a CS-module if and only if N is injective relative to M and both of M and N are CS-modules. As an application, we prove that a direct sum of a non-singular semisimple module and a quasi-continuous module with zero socle is quasi-continuous. This result is known for quasi-injective modules. But when we confine ourselves to CS-modules we need no conditions on their socles. Then we investigate direct sums of CS-modules which are pairwise relatively inective. We show that every finite direct sum of such modules is a CS-module. This result is known for quasi-continuous modules. For the case of infinite direct sums, one has to add an extra condition. Finally, we briefly discuss modules in which every two direct summands are relatively inective.

  8. Separation of 134Cs and 137Cs from 125I solution for medical applications

    International Nuclear Information System (INIS)

    Ram, Ramu; Dash, Ashutosh; Banerjee, Dayamoy

    2015-01-01

    While neutron irradiation of natural Xe gas followed by wet chemical dissolution of activation products constitutes a successful paradigm for the small scale production 125 I, the concomitant production of 134 Cs and 137 Cs emerged as the primary impediment which necessitates purification of 125 I solution. This paper describes an ion-exchange chromatographic technique using Resorcinol Formaldehyde (RF) resin to purify 125 I solution from 134 Cs and 137 Cs impurities. A thorough investigation of the adsorption parameters of RF resin was carried out to arrive at the experimental conditions resulting optimum retention of 134 Cs and 137 Cs impurities. Based on the experimental findings, an optimized separation procedure was developed in which the neutron irradiated dissolved products at pH ∝ 13 was passed through a chromatography column containing RF resin where in 134 Cs and 137 Cs impurities gets adsorbed leaving behind 125 I to appear in the effluent. The overall recovery of 125 I was >90% with acceptable purity amenable for clinical applications.

  9. Sorption of Cs onto γ-Al2O3 using batch technique

    International Nuclear Information System (INIS)

    Wang Xiangke

    2004-01-01

    The sorption of Cs onto γ-Al 2 O 3 is studied by using batch technique, ultra-filtration method and UV vis spectrophotometer at room temperature, pH 4.0, 6.0 and 8.0, the ionic strength of NaClO 4 is from 0.001 mol/L to 0.1 mol/L. The concentration of humic acid in the solution is determined at wavelength of 254 nm. The sorption of humic acid on the γ-Al 2 O 3 is strong (≅98% HA is sorbed on the surface of alumina at pH zpc =9.2)) and strongly dependent on pH values. At pH>9.2, the sorption of HA is decreased markedly with the increasing of pH. Humic acid has a little negative effect on the sorption of Cs onto alumina, this may be attributed to the formation of HA-Cs complexation in the solution. The sorption of Cs onto γ-Al 2 O 3 is weakly dependent on the pH and independent on the ionic strength. Freundlich isotherm can fit the sorption isotherms very well. The sorption of Cs onto γ-Al 2 O 3 may be contributed to cation exchange and surface complexation mechanisms. (authors)

  10. Isolation of 137-Cs in tuna fish by ammonium phosphomolybdate (AMP)

    International Nuclear Information System (INIS)

    Yumiarti; Surtipanti, S.

    1988-01-01

    The isolation of 137-Cs in tuna fish (Neithunnus macroptenus) has been carried out using AMP. The energy of 137-Cs was measure using NaI(T1) detector connected to a Multi Channel Analyzer (MCA). In standard solution of 137-Cs with activity 160.74 and 80.37 pCi, the addition of 120 mg AMP and 7 hours of absorption time, caused 97% of 137-Cs in the solution was absorbed. The destruction of tuna fish was carried out using two methods namely by wet destruction with sulfuric acid, nitrit acid and hydrogen peroxid mixture and by wet destruction with hydrogen peroxide. The applications of this technique of tuna fish was carried out by spiking 137-Cs standard into the fish before being destructed. The recovery obtained from wet destruction with H2O2 was about 80%, while from destruction with acid mixtures and H2O2 was only about 47%. (authors). 3 refs, 3 tabs

  11. Airborne fallout mapping of {sup 137}Cs - STUK/HUT team

    Energy Technology Data Exchange (ETDEWEB)

    Nikkinen, M.; Aarnio, P. [Helsinki Univ. of Technology, Espoo (Finland); Honkamaa, T.; Tiilikainen, H. [Finnish Centre for Radiation and Nuclear Safety, Helsinki (Finland)

    1997-12-31

    The task of the team was to create a fallout map of {sup 137}Cs on a specified area in Padasjoki Auttoinen village. The team used AB-420 helicopter of the Finnish Frontier Guard. The team had two measuring systems: HPGe system (relative efficiency 18%) and NaI system (5`x5`). Both systems produced similar maps. The average {sup 137}Cs fallout within the area (lakes and ponds included) was 88 kBq m{sup -2,} the maximum value being 161 kBq m{sup -2}. In an emergency the HPGe is superior to NaI because of its better energy resolution, giving possibility to obtain nuclide-specific results. (au).

  12. Airborne fallout mapping of {sup 137}Cs - STUK/HUT team

    Energy Technology Data Exchange (ETDEWEB)

    Nikkinen, M; Aarnio, P [Helsinki Univ. of Technology, Espoo (Finland); Honkamaa, T; Tiilikainen, H [Finnish Centre for Radiation and Nuclear Safety, Helsinki (Finland)

    1998-12-31

    The task of the team was to create a fallout map of {sup 137}Cs on a specified area in Padasjoki Auttoinen village. The team used AB-420 helicopter of the Finnish Frontier Guard. The team had two measuring systems: HPGe system (relative efficiency 18%) and NaI system (5`x5`). Both systems produced similar maps. The average {sup 137}Cs fallout within the area (lakes and ponds included) was 88 kBq m{sup -2,} the maximum value being 161 kBq m{sup -2}. In an emergency the HPGe is superior to NaI because of its better energy resolution, giving possibility to obtain nuclide-specific results. (au).

  13. Molecular structures and thermodynamic properties of 12 gaseous cesium-containing species of nuclear safety interest: Cs 2, CsH, CsO, Cs 2O, CsX, and Cs 2X 2 (X = OH, Cl, Br, and I)

    Science.gov (United States)

    Badawi, Michael; Xerri, Bertrand; Canneaux, Sébastien; Cantrel, Laurent; Louis, Florent

    2012-01-01

    Ab initio electronic structure calculations at the coupled cluster level with a correction for the triples extrapolated to the complete basis set limit have been made for the estimation of the thermochemical properties of Cs 2, CsH, CsO, Cs 2O, CsX, and Cs 2X 2 (X = OH, Cl, Br, and I). The standard enthalpies of formation and standard molar entropies at 298 K, and the temperature dependence of the heat capacities at constant pressure were evaluated. The calculated thermochemical properties are in good agreement with their literature counterparts. For Cs 2, CsH, CsOH, Cs 2(OH) 2, CsCl, Cs 2Cl 2, CsBr, CsI, and Cs 2I 2, the calculated ΔfH298K∘ values are within chemical accuracy of the most recent experimental values. Based on the excellent agreement observed between our calculated ΔfH298K∘ values and their literature counterparts, the standard enthalpies of formation at 298 K are estimated to be the following: ΔfH298K∘ (CsO) = 17.0 kJ mol -1 and ΔfH298K∘ (Cs 2Br 2) = -575.4 kJ mol -1.

  14. Evaluation of sorption distribution coefficient of Cs onto granite using sorption data collected in sorption database and sorption model

    International Nuclear Information System (INIS)

    Nagasaki, S.

    2013-01-01

    Based on the sorption distribution coefficients (K d ) of Cs onto granite collected from the JAERI Sorption Database (SDB), the parameters for a two-site model without the triple-layer structure were optimized. Comparing the experimentally measured K d values of Cs onto Mizunami granite carried out by JAEA with the K d values predicted by the model, the effect of the ionic strength on the K d values of Cs onto granite was evaluated. It was found that K d values could be determined using the content of biotite in granite at a sodium concentration ([Na]) of 1 x 10 -2 to 5 x 10 -1 mol/dm 3 . It was suggested that in high ionic strength solutions, the sorption of Cs onto other minerals such as microcline should also be taken into account. (author)

  15. Evaluation of sorption distribution coefficient of Cs onto granite using sorption data collected in sorption database and sorption model

    Energy Technology Data Exchange (ETDEWEB)

    Nagasaki, S., E-mail: nagasas@mcmaster.ca [McMaster Univ., Hamilton, Ontario (Canada)

    2013-07-01

    Based on the sorption distribution coefficients (K{sub d}) of Cs onto granite collected from the JAERI Sorption Database (SDB), the parameters for a two-site model without the triple-layer structure were optimized. Comparing the experimentally measured K{sub d} values of Cs onto Mizunami granite carried out by JAEA with the K{sub d} values predicted by the model, the effect of the ionic strength on the K{sub d} values of Cs onto granite was evaluated. It was found that K{sub d} values could be determined using the content of biotite in granite at a sodium concentration ([Na]) of 1 x 10{sup -2} to 5 x 10{sup -1} mol/dm{sup 3} . It was suggested that in high ionic strength solutions, the sorption of Cs onto other minerals such as microcline should also be taken into account. (author)

  16. The Godparent Plan: A Pedagogical Strategy for CS1 Accompaniment and CS2 Pedagogical Enhancement

    Directory of Open Access Journals (Sweden)

    Pedro Guillermo Feijóo-García

    2018-02-01

    Full Text Available Courses such as CS1 and CS2 can present an interesting pedagogical challenge when it comes to the theory-practice relationship, along with aspects that involve the course's logistics, the programming language used, and the characteristics of the students involved in the process. This study presents an innovative didactic approach, oriented towards the accompaniment of CS1 students by CS2 students at Universidad El Bosque, Colombia, seeking with this Godparent Plan, to provide a personalized accompaniment to first semester students, whereby CS2 students enhance their domain over concepts and skills while accompanying, explaining and teaching younger peers. The results of this study are favorable, outlining a didactic scheme that can be adapted and replicated in other curricular scenarios.

  17. Derivation of 137Cs deposition density from measurement of 137Cs inventories in undisturbed soils

    International Nuclear Information System (INIS)

    Hien, P.D.; Hiep, H.T.; Quang, N.H.; Huy, N.Q.; Binh, N.T.; Hai, P.S.; Long, N.Q.; Bac, V.T

    2012-01-01

    The 137 Cs inventories in undisturbed soils were measured for 292 locations across the territory of Vietnam. the logarithmic inventory values were regressed against characteristics of sampling sites, such as geographical coordinates, annual rainfall and physico-chemical parameters of soil. The regression model containing latitude and annual rainfall as determinants could explain 76% of the variations in logarithmic inventory values across the territory. The model part was interpreted as the logarithmic 137 Cs deposition density. At the 95% confidence level, 137 Cs deposition density could be predicted be the model ± 7% relative uncertainty. the latitude mean 137 Cs deposition density increases northward from 237 Bq m -2 to 1097 Bq m -2 , while the corresponding values derived from the UNSCEAR (1969) global pattern are 300 Bq m -2 and 600 Bq m -2 . High 137 Cs inputs were found in high-rainfall areas in northern and central parts of the territory. (author)

  18. 135Cs/137Cs isotopic composition of environmental samples across Europe: Environmental transport and source term emission applications

    International Nuclear Information System (INIS)

    Snow, Mathew S.; Snyder, Darin C.

    2016-01-01

    135 Cs/ 137 Cs isotopic analyses represent an important tool for studying the fate and transport of radiocesium in the environment; in this work the 135 Cs/ 137 Cs isotopic composition in environmental samples taken from across Europe is reported. Surface soil and vegetation samples from western Russia, Ukraine, Austria, and Hungary show consistent aged thermal fission product 135 Cs/ 137 Cs isotope ratios of 0.58 ± 0.01 (age corrected to 1/1/15), with the exception of one sample of soil-moss from Hungary which shows an elevated 135 Cs/ 137 Cs ratio of 1.78 ± 0.12. With the exception of the outlier sample from Hungary, surface soil/vegetation data are in quantitative agreement with values previously reported for soils within the Chernobyl exclusion zone, suggesting that radiocesium at these locations is primarily composed of homogenous airborne deposition from Chernobyl. Seawater samples taken from the Irish Sea show 135 Cs/ 137 Cs isotope ratios of 1.22 ± 0.11 (age corrected to 1/1/15), suggesting aged thermal fission product Cs discharged from Sellafield. The differences in 135 Cs/ 137 Cs isotope ratios between Sellafield, Chernobyl, and global nuclear weapons testing fallout indicate that 135 Cs/ 137 Cs isotope ratios can be utilized to discriminate between and track radiocesium transport from different nuclear production source terms, including major emission sources in Europe. - Highlights: • 135 Cs/ 137 Cs useful for tracking anthropogenic environmental radiocesium releases. • European surface soils/vegetation have uniform ratio consistent with Chernobyl. • 135 Cs/ 137 Cs in Irish sea represents thermal fission ratio distinct from Chernobyl. • Can distinguish between major source terms in Europe based on 135 Cs/ 137 Cs.

  19. Desorption of 137Cs from Cetraria islandica (L. Ach. using solutions of acids and their salts mixtures

    Directory of Open Access Journals (Sweden)

    ANA A. ČUČULOVIĆ

    2009-06-01

    Full Text Available The desorption of 137Cs from Cetraria islandica (L. Ach. lichen was investigated using the solutions: A H2SO4–HNO3–K2SO4, B H2SO4–HNO3–Na2SO4 and C H2SO4–HNO3– (NH42SO4–(NH4NO3 at pH 2.00, 2.58, 2.87, 3.28 and 3.75, similar to acid rain. After five consecutive desorptions using solutions A, B and C, from 44.0 % (solution B, pH 3.75 to 68.8 % (solution C, pH 3.28 of 137Cs had been desorbed from the lichen. In all cases, the most successful 137Cs desorption was the first one. In the presence of K+ (solution A the total amount of desorbed 137Cs did not depend on the pH of the solution and this was confirmed by the analogous reactions of Cs+ and K+, due to their similar ionic radii. The dependencies of the non-desorbed content of 137Cs on the number of desorptions gave curves indicating that at least two types of sorption occur. One of them can be dominant if suitable desorbants are used. The results indicate lichens as secondary sources of environment pollution with 137Cs.

  20. Modification of the 137Cs, 90Sr, and 60Co transfer to wheat plantlets by NH4+ fertilizers.

    Science.gov (United States)

    Guillén, J; Muñoz-Muñoz, G; Baeza, A; Salas, A; Mocanu, N

    2017-03-01

    Inorganic fertilizers are used as agricultural countermeasures intended to inhibit the soil to plant transfer of radionuclides after a radioactive fallout. Two NH 4 + fertilizers, diammonium phosphate (DAP) and NPK, were applied to soil contaminated with a mixture of radionuclides to analyze whether they modify the transfer of 137 Cs, 90 Sr, and 60 Co and stable elements (K, Na, Ca, and Mg) to wheat plantlets grown under controlled laboratory conditions. DAP introduced NH 4 + in the soil, which can increase 137 Cs transfer, while NPK also introduced K + , which can decrease it. The application of DAP increased the accumulation of 137 Cs in wheat plantlets with increasing application rate, so did the 137 Cs/K in plantlets. Regarding the NPK application, the 137 Cs increased in all treatments, but at maximum rate, the available K introduced by the fertilizer was probably able to partially satisfy the nutritional requirements of the wheat plantlet and the 137 Cs decreased relative to the recommended rate. The 137 Cs/K ratio in plantlet decreased with increasing NPK rates. The transfer of 90 Sr increased with increasing DAP rate and only at the maximum NPK rate. The 60 Co transfer only increased at the maximum application rates for DAP and NPK. These modifications should be considered when using these fertilizers as agricultural countermeasures.

  1. Analysis of ({sup 7}F{sub 0}){gamma}{sub 1g}{yields}({sup 5}D{sub 2}){gamma}{sub 5g}, {gamma}{sub 3g} and ({sup 7}F{sub 0}){gamma}{sub 1g}{yields}({sup 5}L{sub 6}){gamma}{sub 1g}, a{gamma}{sub 5g} two-photon absorption spectra of Cs{sub 2}NaYF{sub 6}:Eu{sup 3+}

    Energy Technology Data Exchange (ETDEWEB)

    Ning Lixin; Wang Dianyuan; Xia Shangda [Structure Research Laboratory, Academica Sinica, Department of Physics, University of Science and Technology of China, Heifei, Anhui (China); Thorne, Jonathan R.G. [Inorganic Chemistry Laboratory, Department of Chemistry, University of Oxford (United Kingdom); Tanner, Peter A. [Department of Biology and Chemistry, City University of Hong Kong, Kowloon (China)

    2002-04-15

    The direct calculation of transition line strengths and relative intensities is presented for two intraconfigurational two-photon absorption (TPA) transitions of Eu{sup 3+} in the cubic Cs{sub 2}NaYF{sub 6} host. Crystal field wavefunctions were utilized for the initial and final f{sup N}-electron states and various approaches were used in constructing all the 4f{sup N-1} 5d{sup 1} intermediate-state wavefunctions. The calculated relative intensities of the ({sup 7}F{sub 0}) {gamma}{sub 1g}{yields}({sup 5}D{sub 2}){gamma}{sub 5g}, {gamma}{sub 3g} TPA transitions are in reasonable agreement with experiment. The neglect of J-mixing in the initial state has only a small effect upon the calculation, whereas the neglect of spin-orbit couplings within the initial and terminal states drastically reduces the calculated transition linestrengths, but does not markedly change the intensity ratios. In the case of the ({sup 7}F{sub 0}){gamma}{sub 1g}{yields}({sup 5}L{sub 6}){gamma}{sub 1g}, a{gamma}{sub 5g} transitions, serious discrepancies between experiment and theory are found if the intermediate states are constructed from a 4f{sup 5} core comprising free ion states and the 5d{sup 1} crystal field states. Satisfactory agreement is, however, found when the 4f{sup 5} crystal field states are utilized in constructing the intermediate states. The contributions to the transition moment have been evaluated for various Hamiltonian terms and the results are discussed. (author)

  2. CS EMISSION NEAR MIR-BUBBLES

    International Nuclear Information System (INIS)

    Watson, C.; Devine, Kathryn; Quintanar, N.; Candelaria, T.

    2016-01-01

    We survey 44 young stellar objects located near the edges of mid-IR-identified bubbles in CS (1–0) using the Green Bank Telescope. We detect emission in 18 sources, indicating young protostars that are good candidates for being triggered by the expansion of the bubble. We calculate CS column densities and abundances. Three sources show evidence of infall through non-Gaussian line-shapes. Two of these sources are associated with dark clouds and are promising candidates for further exploration of potential triggered star formation. We obtained on-the-fly maps in CS (1–0) of three sources, showing evidence of significant interactions between the sources and the surrounding environment

  3. Radiochemical determination of 137Cs in foods

    International Nuclear Information System (INIS)

    Kastner, Geraldo F.; Ferreira, Andrea Vidal; Monteiro, Roberto P.G.

    2013-01-01

    A determination of radionuclides in food samples is important in commodities in order to attend to regulatory requirements for international trade. As a long-lived radioisotope of cesium, 137 Cs is produced as a result of human nuclear activities and than its contamination level evaluation among others radionuclides in foods is necessary. A methodology for the determination of 137 Cs in foods, pork and fish, is described. The procedures covered homogenization and freeze-drying of the samples. The 137 Cs was measured by gamma spectrometry using Canberra 50% HPGe detector. The counting was carried out with Monte Carlo software for detection conditions optimization including geometry and chemical data information. A certified sample, SRM IAEA-375, was analyzed in order to evaluate the reliability of the method, and the results showed good agreement between the measured and certified values. (author)

  4. Retention of 137Cs in three humans

    International Nuclear Information System (INIS)

    Soegaard-Hansen, J.; Lauridsen, B.

    1992-01-01

    In two experiments the retention of 137 Cs after a single intake have been measured with whole-body counting. In the first experiment, two persons ingested a prepared liquid solution of 137 CsCl. In the second experiment these two persons together with a third person ingested 137 Cs naturally incorporated in a piece of meat. The obtained data have been fitted to a retention function with a small compartment having a fast excretion rate and a large compartment having a slow excretion rate, as given by the International Commission on Radiological Protection (ICRP). The effective biological half-lives were in both experiments significantly different from the value given by ICRP. (au)

  5. 137Cs in Norwegian Lapps, spring 1980

    International Nuclear Information System (INIS)

    Westerlund, E.A.; Gjertsen, L.; Lind, B.

    1980-01-01

    Measurements show that the body burden of 137 in Lapps in Norway fell from 1965 to 1975 with an apparent half-life of 4-5 years. Since then the reduction has been considerably slower due to fallout from Chinese nuclear weapon tests. The content of 137 Cs in reindeer meat follows the same pattern. Seasonal variations occur due to the migration of the reindeer between winter grazing on lichen with a high 137 Cs content and summer grazing on grass with a lower 137 Cs content. For annual dose calculations it is found that whole body mearurements at the end of March or the beginning of April give good values. Radiation doses to Lapps working small holdings are about 3/4 of those of nomadic reindeer-herding Lapps. (JIW)

  6. CS EMISSION NEAR MIR-BUBBLES

    Energy Technology Data Exchange (ETDEWEB)

    Watson, C. [Manchester University, Department of Physics, 604 E. College Ave., North Manchester, IN 46962 (United States); Devine, Kathryn [College of Idaho, Department of Physics, 2112 Cleveland Blvd, Caldwell, ID 83605 (United States); Quintanar, N. [Texas A and M University, Department of Nuclear Engineering, 401 Joe Routt Blvd, College Station, TX 77843 (United States); Candelaria, T., E-mail: cwatson@manchester.edu, E-mail: KDevine@collegeofidaho.edu, E-mail: nrquintanar@tamu.edu, E-mail: tcandela@nmt.edu [New Mexico Institute of Mining and Technology, Department of Physics, 801 Leroy Place, Socorro, NM 87801 (United States)

    2016-02-10

    We survey 44 young stellar objects located near the edges of mid-IR-identified bubbles in CS (1–0) using the Green Bank Telescope. We detect emission in 18 sources, indicating young protostars that are good candidates for being triggered by the expansion of the bubble. We calculate CS column densities and abundances. Three sources show evidence of infall through non-Gaussian line-shapes. Two of these sources are associated with dark clouds and are promising candidates for further exploration of potential triggered star formation. We obtained on-the-fly maps in CS (1–0) of three sources, showing evidence of significant interactions between the sources and the surrounding environment.

  7. Cs-137 for irradiation of sewage sludge

    International Nuclear Information System (INIS)

    Lessel, T.

    1986-01-01

    Since 1973, the Geiselbullach sewage treatment works have been continuously operating their first system for gamma irradiation of sewage sludge. Within the framework of a German-American agreement, nine Cs-137 sources with a total activity of 56.000 Ci have been made available to the works free of charge in 1983, in order to test in practice and to demonstrate the applicability of these radiation sources in comparison to the Co-60 sources exclusively used up to then. This first study on the applicability of Cs-137 as a radiation source for sewage sludge treatment revealed no findings or effects speaking against Cs-137 as a radiation source for this purpose. (orig./RB) [de

  8. WESF (173)Cs gamma ray sources

    Science.gov (United States)

    Kenna, B. T.

    1984-10-01

    The Waste Encapsulation and Storage Facility (WESP) at Hanford, Washington has been separating cesium from stored liquid defense waste since 1945. This is done to alleviate the heat generated by the decay of radioactive Cs137. The cesium is converted to CsCl, doubly encapsulated in 316l stainless steel, and placed in storage. The potential utility of these Cs137 capsules as gamma radiation sources was demonstrated. Registration of the capsule with the NRC as a sealed gamma source would facilitate the licensing of non-DOE irradiation facilities using this source. To grant this registration, the NRC requires characteristics of the capsule. It must also be demonstrated that the capsule will maintain its integrity under both normal circumstances and specified abnormal conditions. The required information is provided through collation of results of studies and tests done previously by other laboratories.

  9. Microsphere zeolite materials derived from coal fly ash cenospheres as precursors to mineral-like aluminosilicate hosts for 135,137Cs and 90Sr

    International Nuclear Information System (INIS)

    Vereshchagina, Tatiana A.; Vereshchagin, Sergei N.; Shishkina, Nina N.; Vasilieva, Nataly G.; Solovyov, Leonid A.; Anshits, Alexander G.

    2013-01-01

    Hollow microsphere zeolite materials with a bilayered zeolite/glass crystalline shell bearing NaP1 zeolite were synthesized by the hydrothermal treatment of coal fly ash cenospheres (Si/Al = 2.7) in an alkaline medium. Cs + and/or Sr 2+ forms of zeolitized cenospheres with the different Cs + and/or Sr 2+ loading were prepared by the ion exchange from nitrate solutions. The resulted (Cs,Na)P1, (Sr,Na)P1 and (Cs,Sr,Na)P1 bearing microsphere zeolites were converted to glass ceramics by heating at 900–1000 °C. The differential scanning calorimetry and quantitative phase analysis were used to monitor the solid-phase transformation of the initial and ion exchanged zeolite materials. It was established that the final solidified forms of Cs + and/or Sr 2+ are glass–crystalline ceramic materials based on pollucite–nepheline, Sr-feldspar–nepheline and Sr-feldspar–pollucite composites including ∼60 wt.% of the major host phases (pollucite, Sr-feldspar) and 10–20 wt.% of glass. The 137 Cs leaching rate of 4.1 × 10 −7 g cm −2 day −1 was determined for the pollucite glass–ceramic according to Russian State Standard (GOST) No. 52126 P-2003 (7 day, 25 °C, distilled water)

  10. Phonon dispersion curves for CsCN

    International Nuclear Information System (INIS)

    Gaur, N.K.; Singh, Preeti; Rini, E.G.; Galgale, Jyostna; Singh, R.K.

    2004-01-01

    The motivation for the present work was gained from the recent publication on phonon dispersion curves (PDCs) of CsCN from the neutron scattering technique. We have applied the extended three-body force shell model (ETSM) by incorporating the effect of coupling between the translation modes and the orientation of cyanide molecules for the description of phonon dispersion curves of CsCN between the temperatures 195 and 295 K. Our results on PDCs in symmetric direction are in good agreement with the experimental data measured with inelastic neutron scattering technique. (author)

  11. Mastering Adobe Premiere Pro CS6

    CERN Document Server

    Ekert, Paul

    2013-01-01

    Designed to be practical and engaging, Mastering Adobe Premiere Pro CS6 is a project-based book to help you truly augment your skills and become a film editing hotshot.If you're just starting out or even migrating from existing video editing software, then this book is for you. With rapid progression through practical examples constructed to be both engaging and useful, Mastering Adobe Premiere Pro CS6 is ideal for learning the sometimes complex workflows of this powerful application.

  12. Study of the 137Cs Stabilizer Source

    Directory of Open Access Journals (Sweden)

    GAO Yan;WANG Yan-ling;XU Zhi-jian;XU Liang;REN Chun-xia;TAN Xiao-ming;CUI Hong-qi

    2014-02-01

    Full Text Available The attenuation laws of the Cesium -137 γ-ray penetrating the ceramic core、stainless steel and tungsten steel were studied. The radioactivity of the 137Cs stabilizer source was determined through the surface dose rate of 137Cs stabilizer sources. In addition, the adsorption properties of the ceramic core were studied to improve the stability of the output rate, and established a production line. The application results showed that the output rate of ray source was accurate and was of a good consistency. At present, the source had been used in logging lithology, and achieved the realization of domestic product.

  13. The Photoshop CS4 Companion for Photographers

    CERN Document Server

    Story, Derrick

    2009-01-01

    "Derrick shows that Photoshop can be friendly as well as powerful. In part, he does that by focusing photographers on the essential steps of an efficient workflow. With this guide in hand, you'll quickly learn how to leverage Photoshop CS4's features to organize and improve your pictures."-- John Nack, Principal Product Manager, Adobe Photoshop & BridgeMany photographers -- even the pros -- feel overwhelmed by all the editing options Photoshop provides. The Photoshop CS4 Companion for Photographers pares it down to only the tools you'll need most often, and shows you how to use those tools as

  14. CS model coil experimental log book

    International Nuclear Information System (INIS)

    Nishijima, Gen; Sugimoto, Makoto; Nunoya, Yoshihiko; Wakabayashi, Hiroshi; Tsuji, Hiroshi

    2001-02-01

    Charging test of the ITER CS Model Coil which is the world's largest superconducting pulse coil and the CS Insert Coil had started at April 11, 2000 and had completed at August 18, 2000. In the campaign, total shot numbers were 356 and the size of the data file in the DAS (Data Acquisition System) was over 20 GB. This report is a database that consists of the log list and the log sheets of every shot. One can access the database, make a search, and browse results via Internet (http://1ogwww.naka.jaeri.go.jp). The database will be useful to quick search to choose necessary shots. (author)

  15. Incorporation of {sup 137}Cs by tropical tree species and its correlation with plant physiology

    Energy Technology Data Exchange (ETDEWEB)

    Cid, Alberto Silva; Anjos, Roberto Meigikos dos; Macario, K.D.; Veiga, R.; Ayubi, J. Juri; Lacerda, T. [Universidade Federal Fluminense (UFF), Niteroi, RJ (Brazil). Instituto de Fisica; Zamboni, C.B.; Medeiros, I.M.A. [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN- SP), Sao Paulo, SP (Brazil); Velasco, H.; Rizzotto, M. [Universidad Nacional de San Luis (UNSL) (Argentina). Instituto de Matematica Aplicada San Luis; Audicio, P. [Facultad de Ciencias (UDELAR), Montevideo (Uruguay). Centro de Investigaciones Nucleares

    2011-07-01

    Environmental phenomena associated with potential releases of radionuclides to terrestrial ecosystems have attracted the interest of several researches around the world. However, such interest has not been focused exclusively in its effects on human health. Several radionuclides have also been used as tracers of physicochemical or biological phenomena. These studies depend on both the development of auxiliary analysis techniques, which help to improve the results of traditional methods, and the production of additional data, so that a wide variety of natural processes can be understood. In this sense, the same radiometric results can be analyzed or interpreted from different viewpoints, allowing the interdisciplinary understanding of the overall structure of terrestrial ecosystems. {sup 137}Cs, for example, is one of the main fission products of nuclear reactors and atmospheric nuclear testing that is persistent in the biosphere because of its half-life of 30.2 years and biological mobility. This radionuclide remains in the top soil due to fixation and adsorption to clay minerals and organic matter, persisting in the root zone of plant for a long period of time. As its chemical behavior is similar to other monovalent inorganic cations (such as NH{sup +}{sub 4} , Na{sup +} and K{sup +}), Cs{sup +} can be readily absorbed by roots and translocated to the aboveground parts of plant. In this work, concentrations of {sup 137}Cs{sup +}, K{sup +} and Na{sup +} in fruits of lemon (Citrus limon B.) and coconut (Cocos nucifera L.) were measured by both gamma spectrometry and neutron activation analysis, with the aim to understand the behavior of monovalent inorganic cations in tropical plants as well as the plant ability to store these elements. In contrast to K{sup +} and Na{sup +}, Cs{sup +} is not an essential element to plants. However, our results have shown that {sup 137}Cs{sup +} incorporation to vegetal tissues is positively correlated to K{sup +} distribution inside

  16. Properties of CsI and CsI-TMAE photocathodes

    International Nuclear Information System (INIS)

    Anderson, D.F.; Kwan, S.; Peskov, V.; Hoeneisen, B.

    1992-06-01

    The importance of heating the CsI or CsI-TMAE photocathodes during preparation, as well as the importance of the gas environment on the quantum efficiency is presented. The dependence of the aging characteristics of these photocathodes on the operating temperature, on the presence of gas, and on the charge amplification of the chamber is also discussed. For CsI photocathodes charges in excess of 2x10 14 e - /mm 2 can be collected with little degradation of performance. A timing resolution of 0.55 ns is also achieved for single photoelectrons suggesting a possible time-of-flight detector

  17. Effect of 137Cs on immunological reactivity

    International Nuclear Information System (INIS)

    Shubik, V.M.

    1975-01-01

    An important role of 137 Cs as a new ecological factor was shown by analyzing 31 different studies. The radioisotope may at present be detected in the organisms of all inhabitants of this planet. The migration of 137 Cs along the chain lichen-deer-man leads to its accumulation in the organism of humans living in the Extreme North and taking venison in their food. Although the high sensitivity of immunological reactions to various unfavourable environmental factors is well known, data on the effect of incorporated 137 Cs on immunity are scanty. Experiments on animals showed changes in factors of nonspecific immunity (phagocytic reaction of blood neutrophils, bactericidal activity, lysozyme and complement titres of blood serum) and specific immunity (formation of antiviral antibodies). The blood of animals injured by the isotope displays complete and incomplete autoantibodies. The dependence of immunobiological changes on the dose absorbed by the organism is shown. The 137 Cs intake of inhabitants of the Extreme North who eat venison did not, with the absorbed dose equalling up to 50 Mrem per year, lead to changes in their immunological reactivity. (author)

  18. Flash CS4: The Missing Manual

    CERN Document Server

    Grover, Chris

    2008-01-01

    Unlock the power of Flash and bring gorgeous animations to life onscreen. Flash CS4: The Missing Manual includes a complete primer on animation, a guided tour of the program's tools and capabilities, lots of new illustrations, and more details on working with video. Beginners will learn to use the software in no time, and experienced Flash designers will improve their skills.

  19. Activation energies of diffusion for I and Cs in interlayer of smectite

    International Nuclear Information System (INIS)

    Sato, H.

    2009-01-01

    The apparent diffusivities (Da) and activation energies (ΔEa) for I - and Cs + ions in compacted Na-smectite with an interlayer space of only 2 water layers were measured at a dry density of 1.79 Mg/m 3 . In-diffusion experiments were carried out under the conditions that interlayer space, orientation of smectite stacks and dry density were controlled. Basal spacing was checked by X-ray diffractometry (XRD). All diffraction peaks to d(001) indicated basal spacing, of which interlayer space was equal to 2 water layers. The ΔEa of I - ions was at similar level as that for the ionic diffusivity of I - ions in free water (Do) at a dry density of 1.0 Mg/m 3 , but was 35.24 kJ/mol at a dry density of 1.79 Mg/m 3 . The ΔEa for Cs + ions was 46.27 kJ/mol which was higher than that for I? ions, at a dry density of 1.79 Mg/m 3 . Such high ΔEa for I - ions in the interlayer of smectite could be explained by the lowering in the activity (a H 2 O ) of interlayer water. Since Cs + ions sorb onto smectite by ion exchange, such high ΔEa for Cs + ions could be explained by the combined effects of the Cs+/Na+ ion exchange enthalpy (ΔH o ) in smectite and the lowering in the a H 2 O of interlayer water. (author)

  20. SR-XRF imaging of Cs highly accumulated in vegetables

    International Nuclear Information System (INIS)

    Nakai, Izumi; Oda, Nahoko; Terada, Yasuko

    2011-01-01

    Accumulation of Cs in vegetables was studied with regard to the remediation of radioactive Cs from a nuclear plant accident in Fukushima. It was found that Brassica oleracea var. capitata, Brassica campestris var. perviridis, and Lactuca sativa accumulated Cs to a level of more than 10000 ppm (dry weight) when they were cultivated in 1 mM Cs solution. Two-dimensional distributions of Cs were revealed by SR-XRF imaging showing a homogeneous distribution of Cs in the plant bodies. (author)

  1. Determination of Cs-134 and Cs-137 in different food-stuffs and environmental-stuffs collected from Serina area in Lombardy

    International Nuclear Information System (INIS)

    Rimoldi, E.M.; Di Giancamillo, M.; Cavallone, E.; Brambilla, P.

    1999-01-01

    After the explosion of the reactor n°4 in the Ukrainian Nuclear Power Plant of Chernobyl, the highest radioactive contamination in Italy was observed in Lumbardy. In 1996, ten years after the Chernobyl's accident, the Authors carried out an investigation on soil samples from Serina area, in the district of Bergamo. N°158 samples have been analysed by NaI(Tl) detector (3x3), collected from surface soil and subsoil, running and stagnating waters, mosses, lichens, mushrooms, water-plants, fodder leafage, berries, pine-needles, striated muscle from cattle, sheep, chamois, roe-deer, milk and cheeses from cow and goat, chicken eggs. In all the soil samples analysed Cs-137 was detectable, and its activity was constantly higher in surface soil samples and particularly in those from woods. In May, the seasonal fallout period at our latitudes, it has been detected on Alben Mount a light fallout of Cs-134. In the samples collected on poly-phyto meadows no trace of Cs-137 has been detected, while in samples from wood's ecosystem this isotope was always detectable. Cs-137 was also present in the muds of the bottom of a small natural alpine lake and in water-plants there growing. On the basis of these data the Authors infer that mosses and lichens are the best markers of environmental contamination due to Cs-137. They suggest that it is absolutely necessary to continue to control regularly every substrate included in the food chain and of zootechnic and environmental interest with the following aims: i) to study the capacity of various ecosystems to metabolize the products derived from the Chernobyl's accident; ii) to safeguard the public health against future emergencies: iii) to keep under control foodstuff for human and animal feeding, which, because of the markets' globalization, can arrive from everywhere

  2. Radiation damage in undoped CsI and CsI(Tl)

    International Nuclear Information System (INIS)

    Woody, C.L.; Kierstead, J.A.; Levy, P.W.; Stoll, S.

    1992-01-01

    Radiation damage has been studied in undoped CsI and CsI(TI) crystals using 60 Co gamma radiation for doses up to ∼ 4.2 x 10 6 . Samples from various manufacturers were measured ranging in size from 2.54 cm long cylinders to a 30 cm long block. Measurements were made on the change in optical transmission and scintillation light output as a function of dose. Although some samples showed a small change in transmission, a significant change in light output was observed for all samples. Recovery from damage was also studied as a function of time and exposure to UV light. A short lived phosphorescence was observed in undoped CsI, similar to the phosphorescence seen in CsI(TI)

  3. Ab Initio investigation of cesium monoxide of CsO and CsO+

    International Nuclear Information System (INIS)

    Zialenina, M.; Kelloe, V.; Cernusak, I.

    2015-01-01

    Cesium is material with a low work function and, accordingly, atomic Cs has a low value of ionization energy. Therefore cesium is regarded as a good source material for electrons in plasma heating module. One of plasma heating technologies using Cs grid is foreseen as a candidate for the tokamak within the framework of project ITER. Among the possible impurities that can coexist in this module are CsO or CsO + , due to presence of oxygen traces in the heating chamber. We conducted CCSD(T) energy calculations of the cesium oxide (X 2 Σ + ) and its cation (X 3 Σ - ). Here are presented the bond lengths and spectroscopic parameters of both species and ionization energy (IE). Our IE (6.88 eV) is in good agreement with previous theoretical results, experiment indicates substantially lower value (6.22 eV). (authors)

  4. Measuring 137Cs, 40K and decay products of 226Ra and 232Th in samples of different nature by a multidetector spectrometer

    International Nuclear Information System (INIS)

    Antovic, N.M.; Popovic, V.; Vukotic, P.

    2011-01-01

    A coincidence method for measuring 137 Cs, 40 K, 226 Ra and 232 Th decay products activity in soil, vegetation and fish samples, was applied to the six-crystal gamma-coincidence spectrometer PRIPYAT-2M. In this way, some problems appeared in simultaneous measurement of 137 Cs, 226 Ra and 232 Th by NaI(Tl) detectors and the PRIPYAT-2M spectrometer were solved. The obtained results were agreeable with the HPGe spectrometer ones. (author)

  5. Incorporating Cs and Sr into blast furnace slag inorganic polymers and their effect on matrix properties

    Science.gov (United States)

    Vandevenne, Niels; Iacobescu, Remus Ion; Pontikes, Yiannis; Carleer, Robert; Thijssen, Elsy; Gijbels, Katrijn; Schreurs, Sonja; Schroeyers, Wouter

    2018-05-01

    Minimizing harmful effects to the environment in waste-management practices requires continuous innovation. This is especially important in the field of radioactive waste management. Alternatives to the commonly used ordinary Portland cement matrices are being increasingly studied for improved immobilisation purposes. The development of inorganic polymers (IP) from industrial residues has been successfully studied for the immobilisation of caesium (Cs+) and strontium (Sr2+). However, knowledge of the effect of these introduced elements on the IP-matrix is scarce, especially considering that studied effects are dependent on the IP-precursor characteristics and the form in which the Cs+ and Sr2+ are introduced. In this study, IPs containing varying amounts of CsNO3 and Sr(NO3)2 were developed to study the effect of the introduced elements on the IP-characteristics. IP-samples were developed from ground granulated blast furnace slag (GGBFS) and 6 M NaOH activating solution. Cs+ and Sr2+ were added to account for 0.5, 1 and 2 wt% of the total IP-mass. Throughout the entire study, Cs+-addition showed no significant effects on the studied parameters. Calorimetric results showed that Sr2+ severely affects reaction kinetics, consuming hydroxide ions necessary for the alkali activation reaction. Sr2+-addition also caused a severe decrease in compressive strength, increased calcium leaching, and decreased sodium and hydroxide leaching. Micro-chemical analyses showed that Cs+ is almost fully incorporated in the formed IP-matrix, while Sr2+ mainly precipitates as Sr(OH)2 in concentrated regions throughout the IP-structure. The findings presented in this paper give insights on the effect of contaminant elements on the immobilising matrix.

  6. Transfer of 226Ra, 85Sr and 137Cs from milk to milk products

    International Nuclear Information System (INIS)

    Al-Masri, M.S.; Nashawati, A.; Amin, Y.; Al-Akel, B.

    2006-01-01

    Transfer of 226 Ra, 85 Sr and 137 Cs from cow and sheep milk to various Syrian dairy products has been evaluated. Dairy products include Kashkivan cheese, braided cheese, Haloom cheese, Sircassian cheese, liquid cheese, native cheese, cottage, thick yogurt, butter and milk cream. The results showed that the percentage of 226 Ra, 85 Sr and 137 Cs transferred from cow milk to milk cream (P t = food processing retention factor x processing efficiency x 100%) has reached 32%, 16% and 7%, respectively. Butter and liquid cheese were found to have the lowest percentage of transferred 226 Ra, 85 Sr and 137 Cs. Most of the obtained P t values of the studied radionuclides in thick yogurt were relatively low in spite of the high processing efficiencies of thick yogurt. Moreover, the transfer, P t , of the studied radionuclides from cow milk to the prepared cheese was higher than those values determined for sheep milk. This is due to differences in chemical compositions of each type of milk. On the other hand, the treatment of Native cheese, most commonly consumed cheese in Syria, with different concentrations of NaCl solutions showed that 137 Cs was completely removed from cheese soaking in 5% NaCl solution (soaking time of 48 hours), while 40% of 226 Ra and 80% of 85 Sr were also decontaminated using 0-2.5% NaCl solutions and soaking time of 48 hours. Based on the obtained results, industrialization processes of the dairy products that resulted the removal of radionuclides have been identified. (author)

  7. Calculation of inelastic cross sections for H+ + Cs → H(n=2) + Cs+

    International Nuclear Information System (INIS)

    Valance, A.; Spiess, G.

    1975-01-01

    The cross sections for the processes H + +Cs → H(2p and 2s) +Cs + were calculated in the center of mass energy range 250--2400 eV using a simple pseudopotential formalism for the potential curves and coupling matrix elements and a perturbed stationary state (pss) formulation for the calculation of the cross sections. The results are found to be in reasonable agreement with experiment. (auth)

  8. Determination of Sr-90, Cs-137, Na, K, Cs, Ca, Sr and Ba in Milk Powder (A-7)

    International Nuclear Information System (INIS)

    1973-01-01

    The samples were made from fresh skim milk by spray drying. The homogeneity was achieved by stirring the original liquid milk and the powder itself. No spiking with active or inactive materials was made. Each participating laboratory received 800 g sub-samples of the material. 26 participants submitted a total of 99 laboratory means and 365 results of individual determinations. Some of the laboratories submitted two different sets of results for the same radionuclides or stable elements which were obtained either by different analysts. The results are presented separately for all the radionuclides and stable elements (except cesium)

  9. The 134Cs uptake by sunflower (Helianthus anuus, Less) cultivated on soil contaminated with 134Cs

    International Nuclear Information System (INIS)

    Poppy Intan Tjahaja; Putu Sukmabuana

    2008-01-01

    One of the methods for remediation of contaminated environment is phytoremediation techniques, i.e. the environmental remediation using plants. In this research the bioavailability of sunflower plant (Helianthus anuus, Less) in radiocaesium uptake from soil was studied for being considered as a phytoremediator later. Sunflower plants were cultivated on soil contaminated with 134 Cs with the concentrations of 29,3 kBq/kg ; 117,2 kBq/kg ; 557 kBq/kg for 45 days. As control the sunflowers were also cultivated on non contaminated soil. Observation was carried out every 5 days by sampling 3 plants and soils. The plant and soil samples were dried using infra red lamp for 24 hours, and then counted using gamma spectrometer. The counting results i.e. 134 Cs concentration on soil and plant parts were then analyzed to obtain transfer factor (TF) values. The highest TF values was reached on 26 th day, i.e. 0,87; 1,89 ; 2,82 for initial soil 134 Cs concentrations of 29,3 Bq/g ; 117,2 Bq/g ; 557 Bq/g, respectively. The TF values obtained expressed the capability of plants to accumulate 134 Cs from soils. The observation to the plants growth showed that the plants grew normally on the 134 Cs contaminated soil until the concentration of 557 Bq/g. The sunflower can be considered to be phytoremediator of andosol soil contaminated with Cs radionuclides. (author)

  10. Structure of a highly acidic β-lactamase from the moderate halophile Chromohalobacter sp. 560 and the discovery of a Cs{sup +}-selective binding site

    Energy Technology Data Exchange (ETDEWEB)

    Arai, Shigeki; Yonezawa, Yasushi; Okazaki, Nobuo; Matsumoto, Fumiko; Shibazaki, Chie; Shimizu, Rumi; Yamada, Mitsugu; Adachi, Motoyasu; Tamada, Taro [Japan Atomic Energy Agency, 2-4 Shirakata-shirane, Tokai, Ibaraki 319-1195 (Japan); Kawamoto, Masahide [Kyushu Synchrotron Light Research Center, 8-7 Yayoigaoka, Tosu, Saga 841-0005 (Japan); Tokunaga, Hiroko; Ishibashi, Matsujiro [Faculty of Agriculture, Kagoshima University, 1-21-24 Korimoto, Kagoshima 890-0065 (Japan); Blaber, Michael [Japan Atomic Energy Agency, 2-4 Shirakata-shirane, Tokai, Ibaraki 319-1195 (Japan); Florida State University, 1115 West Call Street, Tallahassee, FL 32306-4300 (United States); Tokunaga, Masao [Faculty of Agriculture, Kagoshima University, 1-21-24 Korimoto, Kagoshima 890-0065 (Japan); Kuroki, Ryota, E-mail: kuroki.ryota@jaea.go.jp [Japan Atomic Energy Agency, 2-4 Shirakata-shirane, Tokai, Ibaraki 319-1195 (Japan)

    2015-03-01

    The tertiary structure of a β-lactamase derived from the halobacterium Chromohalobacter sp. 560 (HaBLA) was determined by X-ray crystallography. Three unique Sr{sup 2+}-binding sites and one Cs{sup +}-binding site were discovered in the HaBLA molecule. Environmentally friendly absorbents are needed for Sr{sup 2+} and Cs{sup +}, as the removal of the radioactive Sr{sup 2+} and Cs{sup +} that has leaked from the Fukushima Nuclear Power Plant is one of the most important problems in Japan. Halophilic proteins are known to have many acidic residues on their surface that can provide specific binding sites for metal ions such as Cs{sup +} or Sr{sup 2+}. The crystal structure of a halophilic β-lactamase from Chromohalobacter sp. 560 (HaBLA) was determined to resolutions of between 1.8 and 2.9 Å in space group P3{sub 1} using X-ray crystallography. Moreover, the locations of bound Sr{sup 2+} and Cs{sup +} ions were identified by anomalous X-ray diffraction. The location of one Cs{sup +}-specific binding site was identified in HaBLA even in the presence of a ninefold molar excess of Na{sup +} (90 mM Na{sup +}/10 mM Cs{sup +}). From an activity assay using isothermal titration calorimetry, the bound Sr{sup 2+} and Cs{sup +} ions do not significantly affect the enzymatic function of HaBLA. The observation of a selective and high-affinity Cs{sup +}-binding site provides important information that is useful for the design of artificial Cs{sup +}-binding sites that may be useful in the bioremediation of radioactive isotopes.

  11. Structure of a highly acidic β-lactamase from the moderate halophile Chromohalobacter sp. 560 and the discovery of a Cs+-selective binding site

    International Nuclear Information System (INIS)

    Arai, Shigeki; Yonezawa, Yasushi; Okazaki, Nobuo; Matsumoto, Fumiko; Shibazaki, Chie; Shimizu, Rumi; Yamada, Mitsugu; Adachi, Motoyasu; Tamada, Taro; Kawamoto, Masahide; Tokunaga, Hiroko; Ishibashi, Matsujiro; Blaber, Michael; Tokunaga, Masao; Kuroki, Ryota

    2015-01-01

    The tertiary structure of a β-lactamase derived from the halobacterium Chromohalobacter sp. 560 (HaBLA) was determined by X-ray crystallography. Three unique Sr 2+ -binding sites and one Cs + -binding site were discovered in the HaBLA molecule. Environmentally friendly absorbents are needed for Sr 2+ and Cs + , as the removal of the radioactive Sr 2+ and Cs + that has leaked from the Fukushima Nuclear Power Plant is one of the most important problems in Japan. Halophilic proteins are known to have many acidic residues on their surface that can provide specific binding sites for metal ions such as Cs + or Sr 2+ . The crystal structure of a halophilic β-lactamase from Chromohalobacter sp. 560 (HaBLA) was determined to resolutions of between 1.8 and 2.9 Å in space group P3 1 using X-ray crystallography. Moreover, the locations of bound Sr 2+ and Cs + ions were identified by anomalous X-ray diffraction. The location of one Cs + -specific binding site was identified in HaBLA even in the presence of a ninefold molar excess of Na + (90 mM Na + /10 mM Cs + ). From an activity assay using isothermal titration calorimetry, the bound Sr 2+ and Cs + ions do not significantly affect the enzymatic function of HaBLA. The observation of a selective and high-affinity Cs + -binding site provides important information that is useful for the design of artificial Cs + -binding sites that may be useful in the bioremediation of radioactive isotopes

  12. Baseline quantity of 131I, 137Cs, 134Cs and 40K in urinary excretions from Thai people and internal exposure dose

    Science.gov (United States)

    Peekhunthod, D.; Bangvirunrak, J.; Sansakon, S.; Nukultham, A.; Pukkhaw, T.

    2017-06-01

    Today, sealed and unsealed radioactive materials have been used in Thailand for various purposes such as medical, agricultural and industrial applications. There is a growing trend in the use of radioactive materials. Moreover, neighboring countries are planning to construct and operate nuclear power plants. In case of nuclear power plant accidents, radioactive releases in environment and intakes into human body by inhalation and ingestion causing long term health effects. This research aims to determine the radiation baseline quantity of interested relevant radionuclides such as 131I, 137Cs, 134Cs as well as a natural radionuclide, 40K in urine samples of Thai people by gamma spectrometry. Two types of detectors (NaI and HpGe detectors) are calibrated by mixed radionuclide standards of 109Cd, 57Co, 133Ba, 54Mn, 137Cs and 60Co, (energy range from 88 to 1,331 keV). 720 urine samples are collected over a 24 hour period from Thai volunteers with the age older than 18 years old, who lived in eight locations of Thailand. To reduce the effect of geometric difference, 30 ml of urine samples are prepared for counting measurement and efficiency determination. The radiation baseline quantity of 131I, 137Cs, 134Cs and 40K in 30 ml of urine samples are 0.37±0.09, 0.63±0.13, 0.39±0.08 and 7.84±1.63 Bq, respectively. Based on the assumption of intake (50% of the intake by ingestion and 50% of the intake by inhalation), internal dose for members of public are assessed. The committed dose equivalent due to an intake of 131I, 137Cs, 134Cs and 40K are 2.36E-03±1.66-03, 1.15E-01±8.61E-02, 1.16E-01±7.77E-02, 9.44E-01±3.56E-01 mSv per year, respectively.

  13. Electrodriven selective transport of Cs+ using chlorinated cobalt dicarbollide in polymer inclusion membrane: a novel approach for cesium removal from simulated nuclear waste solution.

    Science.gov (United States)

    Chaudhury, Sanhita; Bhattacharyya, Arunasis; Goswami, Asok

    2014-11-04

    The work describes a novel and cleaner approach of electrodriven selective transport of Cs from simulated nuclear waste solutions through cellulose tri acetate (CTA)/poly vinyl chloride (PVC) based polymer inclusion membrane. The electrodriven cation transport together with the use of highly Cs+ selective hexachlorinated derivative of cobalt bis dicarbollide, allows to achieve selective separation of Cs+ from high concentration of Na+ and other fission products in nuclear waste solutions. The transport selectivity has been studied using radiotracer technique as well as atomic emission spectroscopic technique. Transport studies using CTA based membrane have been carried out from neutral solution as well as 0.4 M HNO3, while that with PVC based membrane has been carried out from 3 M HNO3. High decontamination factor for Cs+ over Na+ has been obtained in all the cases. Experiment with simulated high level waste solution shows selective transport of Cs+ from most of other fission products also. Significantly fast Cs+ transport rate along with high selectivity is an interesting feature observed in this membrane. The current efficiency for Cs+ transport has been found to be ∼100%. The promising results show the possibility of using this kind of electrodriven membrane transport methods for nuclear waste treatment.

  14. Fission products behavior in molten fluoride salts: Speciation of La{sup 3+} and Cs{sup +} in melts containing oxide ions

    Energy Technology Data Exchange (ETDEWEB)

    Rollet, Anne-Laure [CEMHTI, Conditions Extremes et Materiaux: Haute Temperature et Irradiation, CNRS, Universite d' Orleans, 1D avenue de la recherche scientifique, 45071 Orleans cedex 2 (France); PECSA, Physico-chimie des Electrolytes, Colloiedes et Sciences Analytiques, CNRS-UPMC-ESPCI, 4 place Jussieu, 75005 Paris (France); Veron, Emmanuel [CEMHTI, Conditions Extremes et Materiaux: Haute Temperature et Irradiation, CNRS, Universite d' Orleans, 1D avenue de la recherche scientifique, 45071 Orleans cedex 2 (France); Bessada, Catherine, E-mail: catherine.bessada@cnrs-orleans.fr [CEMHTI, Conditions Extremes et Materiaux: Haute Temperature et Irradiation, CNRS, Universite d' Orleans, 1D avenue de la recherche scientifique, 45071 Orleans cedex 2 (France)

    2012-10-15

    Graphical abstract: - Abstract: In this paper we address the effects of fission products on the speciation in molten fluoride salts. Numerous systems with cross-connections have been investigated in order to better identify the influence of CsF in a fluoride melt containing rare earth and oxides : LaF{sub 3}-AF (A = Li, Na, K, Rb and Cs), LaF{sub 3}-LiF-CsF, LaF{sub 3}-LiF-CaF{sub 2}, LaF{sub 3}-LiF-CaO, LaF{sub 3}-LiF-CaO-CsF. In this goal, we performed high temperature NMR experiments and followed in situ the evolution of {sup 19}F, {sup 23}Na, {sup 85}Rb, {sup 133}Cs and {sup 139}La NMR chemical shifts. In LaF{sub 3}-AF-CsF and LaF{sub 3}-AF-CaF{sub 2} systems, the coordination number of lanthanum cation ranges from 6 to 8 depending on the LaF{sub 3} concentration and on the polarizability of the other cations. The addition of oxide (CaO) in the latter mixtures leads to the formation of lanthanum oxyfluoride species that precipitate in LaOF when CaO concentration is increased. The addition of CsF to LaF{sub 3}-LiF-CaO yields to a displacement of the dissolved versus precipitated LaOF proportion.

  15. Biological effects of 137Cs, incorporated into organism of rats

    International Nuclear Information System (INIS)

    Monakhov, A.S.; Strekalov, S.A.; Sokolov, A.V.; Aver'yanova, T.K.

    1987-01-01

    Results of investigating mutagenous and hemotoxic effects of 137 Cs on blood lymphocytes of rats are presented. 137 Cs was orally administrated into organism of rats as 270 kBq/g chloride solution. 137 Cs mutagenous effect was studied on metaphase plates of rat blood lymphocytes in course of rats lifetime experiment. It is stated that 137 Cs inducing severe disturbances of genetic material in a great quantity of blood lymphocytes, causes their total killing

  16. Synthesis, thermal decomposition and sensitivity study of CsDNBF

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Shaozong; Zhang, Tonglai; Yang, Li; Zhang, Jianguo; Sun, Yuanhua [State Key Laboratory of Explosion Science and Technology, Beijing Institute of Technology, Beijing 100081 (China)

    2007-02-15

    CsDNBF (cesium 7-hydroxy-4,6-dinitro-5,7-dihydrobenzofuroxanide) was synthesized from the sodium salt of DNBF and cesium nitrate. The thermal decomposition process has been investigated and the results show that the solid residues at 240 C are RCOOCs, CsNCO, RNO{sub 2} and CsNO{sub 3}. The sensitivity results demonstrate that CsDNBF has better properties than KDNBF, which has been widely used. (Abstract Copyright [2007], Wiley Periodicals, Inc.)

  17. CS model coil experimental log book

    Energy Technology Data Exchange (ETDEWEB)

    Nishijima, Gen; Sugimoto, Makoto; Nunoya, Yoshihiko; Wakabayashi, Hiroshi; Tsuji, Hiroshi [Japan Atomic Energy Research Inst., Naka, Ibaraki (Japan). Naka Fusion Research Establishment

    2001-02-01

    Charging test of the ITER CS Model Coil which is the world's largest superconducting pulse coil and the CS Insert Coil had started at April 11, 2000 and had completed at August 18, 2000. In the campaign, total shot numbers were 356 and the size of the data file in the DAS (Data Acquisition System) was over 20 GB. This report is a database that consists of the log list and the log sheets of every shot. One can access the database, make a search, and browse results via Internet (http://1ogwww.naka.jaeri.go.jp). The database will be useful to quick search to choose necessary shots. (author)

  18. Magnetic correlations in CsVBr3

    International Nuclear Information System (INIS)

    Itoh, Shinichi; Kakurai, Kazuhisa; Endoh, Yasuo

    2001-01-01

    The static magnetic correlation function, S(q), in and S=3/2, one-dimensional Heisenberg antiferromagnet, CsVBr 3 , was measured at temperatures between 40 K and 200 K above the three-dimensional ordering temperature (T N =20.3 K), on a chopper spectrometer install at a pulsed neutron source. The observed S(q) was well fitted to a Lorentzian function convoluted with the instrumental resolution function. The inverse correlation length, κ(T), determined as a half width of the correlation function, showed a linear temperature dependence in the observed temperature range, and, qualitatively well agreed with classical theory. This is consistent with current theory, also, with κ(T) reported for a similar system, CsVCl 3 . (author)

  19. 137Cs behaviour in fruit trees

    International Nuclear Information System (INIS)

    Monte, L.; Quaggia, S.; Pompei, F.; Fratarcangeli, S.

    1989-01-01

    The results of measurements carried out during the period 1987-1988, to evaluate the levels of 137 Cs and 134 Cs contamination in fruit samples and in various components of fruit-trees have been reported. It has been demonstrated that, in the case of an accidental contamination of the air, the contamination of fruit is mainly due to the foliar translocation of radionuclide. Data of radioactivity content in fruits collected through a period of three years show that the radioactivity content in fruit diminishes exponentially. Rough estimates of ''translocation coefficient'' defined as the ratio (radionuclide concentration in fruit)/(radionuclide deposition on soil), and of the ''biological half time'' have been carried out in the case of hazel-nut, walnut, apple, chestnut and olive

  20. Teaching the Five Cs with Cinema

    Directory of Open Access Journals (Sweden)

    Rimma Garn

    2012-08-01

    Full Text Available This paper discusses teaching the five Cs (as noted in the following introduction, delineated in the “National Standards for Foreign Language Learning in the 21st Century,” through a college content course based on cinema. It provides an overview of a 2009 Berkeley workshop, “Teaching Language and Culture with Film,” that addressed larger issues related to such courses within the curriculum, their design and teaching. The paper goes on to describe three Russian courses based on the same textbook, KinoTalk, yet designed for different student audiences: for traditional third year students and for various kinds of non-traditional students, for heritage speakers, and for former missionaries with two-years experience in the target country but minimal formal training in the language. In conclusion, the paper suggests ideas for further courses taught using the same textbook and for teaching the five Cs through language and cinema in general.

  1. Activity of 137Cs in Forest Mushrooms in Poland in 2000

    International Nuclear Information System (INIS)

    Grabowski, D.; Kurowski, W.; Muszynski, W.; Rubel, B.; Smagala, G.; Swietochowska, J.

    2001-01-01

    Full text: The radiocaesium in mushrooms has been monitored in Poland after the Chernobyl accident. The samples of mushrooms were collected all over the territory of Poland during the period 1986-2000. Activity of 137 Cs was much higher than in other foodstuff. This is connected with specific forest ecosystem and tendency to accumulate caesium by some kinds of mushrooms. The significant variations were observed in different species of mushrooms collected at the same area and time. This paper presents the activity of 137 Cs in Xerocomus badius, Boletus edulis and Cantharellus cibarius in Poland in 2000. The samples had been analysed during mushroom-season (June-September). Activities of 137 Cs were measured by gamma spectrometry with HPGe or NaI(Tl) detectors. The activity of 137 Cs was in range 24-472 Bq/kg for Xerocomus badius, 1-678 Bq/kg for Boletus edulis and 1-557 Bq/kg for Cantharellus cibarius. The results were compared to the data from previous years. (author)

  2. On Gács' quantum algorithmic entropy

    Directory of Open Access Journals (Sweden)

    Toru Takisaka

    2014-12-01

    Full Text Available We define an infinite dimensional modification of lower-semicomputability of density operators by Gács with an attempt to fix some problem in the paper. Our attempt is partly achieved by showing the existence of universal operator under some additional assumption. It is left as a future task to eliminate this assumption. We also see some properties and examples which stimulate further research. In particular, we show that universal operator has certain nontrivial form if it exists.

  3. Flash CS3 The Missing Manual

    CERN Document Server

    Grover, Chris

    2008-01-01

    Flash CS3, the latest version of the premier tool for creating web animations and interactive web sites, can be intimidating to learn. This entertaining reference tutorial provides a reader-friendly animation primer and a guided tour of all the program's tools and capabilities. Beginners will learn to use the software in no time, and experienced users will quickly take their skills to the next level.

  4. 137Cs in Research Polygon 'Sumbar'

    International Nuclear Information System (INIS)

    Skoko, B.; Marovic, G.; Babic, D.; Vickovic, I.

    2011-01-01

    In 2009, Radiation Protection Unit of the Institute for Medical Reseach and Occupational Health started a radioactivity measurement programme in research polygon ''Sumbar''. The purpose of these investigations is to collect as many data as possible about the contamination of the polygon that is mainly covered by a forest of English oak (Quercus robur) and hornbeam (Carpinus betulus). Once contaminated, forests represent long-term sources of radiation exposure to specific population groups which are using them as a source of foodstuffs. After the Chernobyl accident, researchers have shown that there has been more variability in radionuclide activity concentration in forests than in agricultural ecosystems. In order to carry out a radioactivity screening of the polygon, we randomly chosed three sampling sites for collecting soil, grass and moss samples. Different species of mushrooms were collected over the whole polygon area. The average activity concentration of 137Cs in soil for two sampling sites is (123 @ 9) Bq kg -1 , while the result for the third site is lower by an order of magnitude ((16.1@0.5) Bq kg -1 ). The activity concentration of 137Cs in grass samples ranges from (0.43 @ 0.03) Bq kg -1 to (13.2 @ 0.1) Bq kg -1 , and in moss samples from (8.7 @ 0.2) Bq kg -1 to (57.8 @ 0.3) Bq kg - 1. In five collected mushroom species, the activity of 137Cs is in the range between (4.1 @ 0.5) Bq kg -1 and (610 @ 5) Bq kg -1 , the lowest and the highest values referreing to Clitocybe nebularis and Gymnopus dryophilus, respectively. Parasitic mushrooms exhibit activity below the minimum detection level. Our preliminary results show and confirm variability of the activity concentration of 137Cs in different parts of this ecosystem. (author)

  5. Fractionation of 137Cs and Pu in natural peatland

    International Nuclear Information System (INIS)

    Mihalík, Ján; Bartusková, Miluše; Hölgye, Zoltán; Ježková, Tereza; Henych, Ondřej

    2014-01-01

    High Cs-137 concentrations in plants growing on peatland inspired us to investigate the quantity of its bioavailable fraction in natural peat. Our investigation aims to: a) estimate the quantity of bioavailable Cs-137 and Pu present in peat, b) verify the similarity of Cs-137 and K-40 behaviours, and c) perform a quantification of Cs-137 and Pu transfer from peat to plants. We analysed the vertical distribution of Cs-137 and Pu isotopes in the peat and their concentrations in plants growing on these places. Bioavailability of radionuclides was investigated by sequential extraction. Sequential analyses revealed that it was the upper layer which contained the majority of Cs-137 in an available form while deeper layers retained Cs-137 in immobile fractions. We can conclude that 18% of all Cs-137 in the peat is still bioavailable. Despite of the low quantity of bioavailable fraction of Cs-137 its transfer factor reached extremely high values. In the case of Pu, 64% of its total amount was associated with fulvic/humic acids which resulted in the high transfer factor from peat to plants. 27 years after the Chernobyl nuclear accident, the significant part of radionuclides deposited in peatland is still bioavailable. - Highlights: • Decrease of exchangeable 137 Cs and its increase in residual fraction with depth. • High 137 Cs transfer factor contrary to its low quantity in bioavailable fractions. • Fulvic/humic acids are a more effective carrier for Pu than for Cs

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

    International Nuclear Information System (INIS)

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

    1998-01-01

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

  7. Development of certified matrix reference materials for quality assurance of screening 134Cs and 137Cs in food

    International Nuclear Information System (INIS)

    Ishizu, H.; Yamada, T.

    2013-01-01

    A certified reference material using activated alumina powder certified for activity of 134 Cs and 137 Cs was developed. The results of the verification and the certification are described. The certified reference material can be used for quality assurance of screening activity measurements of 134 Cs and 137 Cs in food/foodstuffs. Commercially available equipments were experimentally tested using the CRM and another CRM including 40 K. The results of these tests are also shown. - Highlights: • CRM of 134 Cs and 137 Cs using activated alumina was developed. • CRM including 134 Cs, 137 Cs and 40 K was also developed. • Results of experimental performance test of commercial inspection equipments using CRMs were shown

  8. Cesium platinide hydride 4Cs{sub 2}Pt.CsH: an intermetallic double salt featuring metal anions

    Energy Technology Data Exchange (ETDEWEB)

    Smetana, Volodymyr [Ames Laboratory, US Department of Energy, and Critical Materials Institute, Ames, Iowa, 50011-3020 (United States); Mudring, Anja-Verena [Ames Laboratory, US Department of Energy, and Critical Materials Institute, Ames, Iowa, 50011-3020 (United States); Department of Materials Sciences and Engineering, Iowa State University, Ames, Iowa, 50011-3111 (United States)

    2016-11-14

    With Cs{sub 9}Pt{sub 4}H a new representative of ionic compounds featuring metal anions can be added to this rare-membered family. Cs{sub 9}Pt{sub 4}H exhibits a complex crystal structure containing Cs{sup +} cations, Pt{sup 2-} and H{sup -} anions. Being a red, transparent compound its band gap is in the visible range of the electromagnetic spectrum and the ionic type of bonding is confirmed by quantum chemical calculations. This cesium platinide hydride can formally be considered as a double salt of the ''alloy'' cesium-platinum, or better cesium platinide, Cs{sub 2}Pt, and the salt cesium hydride CsH according to Cs{sub 9}Pt{sub 4}H≡4 Cs{sub 2}Pt.CsH. (copyright 2016 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

  9. Residual contamination from Cs-137 in the Sondrio area (Lombardy - Italy)

    International Nuclear Information System (INIS)

    Rimoldi, E.M.; Leonardi, L.; Cavallone, E.; Bignazzi, R.; Galimberti, A.

    2000-01-01

    The authors conducted the investigations on the contamination by Cs-137, resulting from Chernobyl's Accident, in the Sondrio area (Lombardy, Italy). Analyses were performed with NaI (T1) spectrometer. 130 samples collected from superficial earth layer (up to 15 cm) and deep earth layer (from 15 to 30 cm) of woods and meadows, pond's mud, mosses, mushrooms, wild wood fruits, forages, striated muscle from deer, chamois and roe deer, goat's and cow's milk, and running and stagnant water, were studied. Superficial earth samples always showed a higher Cs-137 concentration compared to deep earth samples, their mean activities being 68 Bq/kg (sup. wood) and 18 Bq/kg (sup. meadow). In 1 sample from superficial wood earth in Val Belsivo, the concentration was 1109 Bq/kg. The mud samples had a mean Cs-137 concentration of 96 Bq/kg. Cs-137 was always present in mosses with a mean activity of 234 Bq/kg, whereas in mushrooms contamination was continuous (mean, 63 Bq/kg). Cs-137 was absent in wild wood fruits and in forages except for one sample of bilberry (12 Bq/Kg) and one sample of forage (54 Bq/Kg). In the striated muscle samples from wild animals, chamois always showed high Cs-137 concentration (29 Bq/kg), but was intermediate in roe deer (18 Bq/kg) and lowest in deer (5 Bq/kg). In 4 deer and 4 roe deer, contamination was undetectable. Running and stagnant waters, and cow's milk were not contaminated whereas some Cs-137 activities were detected in goat milk samples (18 Bq/kg). It is concluded that residual contamination from Chernobyl's accident in the investigated areas has by now just become a scientific interest and no longer a sanitary issue, as the contamination levels detected in all the samples are clearly below the maximal admissible levels established by the European Gazettes. However, it is interesting to note that the recycling of Cs-137 is more present in wood, confirming the delicate environmental balance of this ecosystem. The routine radio

  10. Pharmacological profile of CS-3150, a novel, highly potent and selective non-steroidal mineralocorticoid receptor antagonist.

    Science.gov (United States)

    Arai, Kiyoshi; Homma, Tsuyoshi; Morikawa, Yuka; Ubukata, Naoko; Tsuruoka, Hiyoyuki; Aoki, Kazumasa; Ishikawa, Hirokazu; Mizuno, Makoto; Sada, Toshio

    2015-08-15

    The present study was designed to characterize the pharmacological profile of CS-3150, a novel non-steroidal mineralocorticoid receptor antagonist. In the radioligand-binding assay, CS-3150 inhibited (3)H-aldosterone binding to mineralocorticoid receptor with an IC50 value of 9.4nM, and its potency was superior to that of spironolactone and eplerenone, whose IC50s were 36 and 713nM, respectively. CS-3150 also showed at least 1000-fold higher selectivity for mineralocorticoid receptor over other steroid hormone receptors, glucocorticoid receptor, androgen receptor and progesterone receptor. In the reporter gene assay, CS-3150 inhibited aldosterone-induced transcriptional activation of human mineralocorticoid receptor with an IC50 value of 3.7nM, and its potency was superior to that of spironolactone and eplerenone, whose IC50s were 66 and 970nM, respectively. CS-3150 had no agonistic effect on mineralocorticoid receptor and did not show any antagonistic or agonistic effect on glucocorticoid receptor, androgen receptor and progesterone receptor even at the high concentration of 5μM. In adrenalectomized rats, single oral administration of CS-3150 suppressed aldosterone-induced decrease in urinary Na(+)/K(+) ratio, an index of in vivo mineralocorticoid receptor activation, and this suppressive effect was more potent and longer-lasting than that of spironolactone and eplerenone. Chronic treatment with CS-3150 inhibited blood pressure elevation induced by deoxycorticosterone acetate (DOCA)/salt-loading to rats, and this antihypertensive effect was more potent than that of spironolactone and eplerenone. These findings indicate that CS-3150 is a selective and highly potent mineralocorticoid receptor antagonist with long-lasting oral activity. This agent could be useful for the treatment of hypertension, cardiovascular and renal disorders. Copyright © 2015 Elsevier B.V. All rights reserved.

  11. Approaches to contamination problems of agricultural land using Na(I) Tl spectrometer and gamma camera

    International Nuclear Information System (INIS)

    Yin, Yong-Gen; Suzui, Nobuo; Kawachi, Naoki; Ishii, Satomi; Fujimaki, Shu; Yamaguchi, Mitsutaka; Tanoi, Keitaro; Nakanishi, Tomoko M.; Chino, Mitsuo; Nakamura, Shin-ichi; Watabe, Hiroshi; Yamamoto, Seiichi

    2012-01-01

    The severe accident of Fukushima Daiichi Nuclear Power Plant made a large area of agricultural land contaminated with radioactive cesium (Cs-134 and 137). Quantitative analysis for radioactivity (discriminating for Cs-134 and Cs-137) taken in vegetables from the land was carried out using NaI (Tl) scintillation spectrometer. Development of gamma camera for their imaging due to Cs 137 was performed. The shape of the peaks in the spectrum, baseline suppression, a solution of lines overlapping, enhancement of high-resolution were studied. Furthermore, the effect of water on cesium absorbing and transferring process from the root to the tissue was studied. (S. Ohno)

  12. Using Multiple Paths in NoCs for Guaranteed Resource Allocation and Improved Best Effort Performance in NoCs.

    NARCIS (Netherlands)

    Ovadia, I.; Ha, Y.; Corporaal, H.

    2005-01-01

    Networks-on-Chips (NoCs) provide communication platforms to Systems-on-Chips (SoCs). In NoCs, channels are generally shared between traffic flows, resulting in contention. However, certain flows require delivery guarantees. Differentiated quality-of-service (QoS) is achieved by providing guaranteed

  13. Absorption and backscatter of internal conversion electrons in the measurements of surface contamination of 137Cs

    International Nuclear Information System (INIS)

    Yunoki, A.; Kawada, Y.; Yamada, T.; Unno, Y.; Sato, Y.; Hino, Y.

    2013-01-01

    We measured 4π and 2π counting efficiencies for internal conversion electrons (ICEs), gross β-particles and also β-rays alone with various source conditions regarding absorber and backing foil thickness using e-X coincidence technique. Dominant differences regarding the penetration, attenuation and backscattering properties among ICEs and β-rays were revealed. Although the abundance of internal conversion electrons of 137 Cs- 137 Ba is only 9.35%, 60% of gross counts may be attributed to ICEs in worse source conditions. This information will be useful for radionuclide metrology and for surface contamination monitoring. - Highlights: • Counting efficiencies for internal conversion electrons from 137 Cs were measured, and compared with those for β-rays. • Electron-X coincidence technique was employed. • A thin NaI(Tl) scintillation detector was used for X-ray detection. • Backscattering fractions of electrons and beta particles were studied by similar experiments

  14. New compounds bearing [M(S{sub 2}O{sub 7}){sub 3}]{sup 2-} anions (M = Si, Ge, Sn): Syntheses and characterization of A{sub 2}[Si(S{sub 2}O{sub 7}){sub 3}] (A = Na, K, Rb), A{sub 2}[Ge(S{sub 2}O{sub 7}){sub 3}] (A = Li, Na, K, Rb, Cs), A{sub 2}[Sn(S{sub 2}O{sub 7}){sub 3}] (A = Na, K), and the unique germanate Hg{sub 2}[Ge(S{sub 2}O{sub 7}){sub 3}]Cl{sub 2} with cationic {sup 1}{sub ∞}[HgCl{sub 2/2}]{sup +} chains

    Energy Technology Data Exchange (ETDEWEB)

    Logemann, Christian; Witt, Julia; Wickleder, Mathias S. [Universitaet Oldenburg, Institut fuer Reine und Angewandte Chemie (Germany); Gunzelmann, Daniel; Senker, Juergen [Universitaet Bayreuth, Lehrstuhl fuer Anorganische Chemie III (Germany)

    2012-10-15

    The reaction of the group 14 tetrachlorides MCl{sub 4} (M = Si, Ge, Sn) with oleum (65 % SO{sub 3}) at elevated temperatures led to the unique anionic complexes [M(S{sub 2}O{sub 7}){sub 3}]{sup 2-} that show the central M atoms in coordination of three chelating S{sub 2}O{sub 7}{sup 2-} groups. The mean distances M-O within the complexes increase from 175 pm (M = Si) via 186 pm (M = Ge) up to 200 pm (M = Sn). The charge balance for the [M(S{sub 2}O{sub 7}){sub 3}]{sup 2-} anions is achieved by alkaline metal ions A{sup +} (A = Li, Na, K, Rb, Cs) which were implemented in the syntheses in form of their sulfates. The size of the A{sup +} ions, i.e. their coordination requirement causes the crystallographic differences in the crystal structures, while the structure of the complex [M(S{sub 2}O{sub 7}){sub 3}]{sup 2-} anions remains essentially unaffected. Furthermore, we were able to characterize the unique germanate Hg{sub 2}[Ge(S{sub 2}O{sub 7}){sub 3}]Cl{sub 2} which forms when HgCl{sub 2} is added as a source for the counter cation. The Hg{sup 2+} and the Cl{sup -} ions form infinite cationic chains according to {sup 1}{sub ∞}[HgCl{sub 2/2}]{sup +} which take care for the charge compensation. For selected examples of the compounds the thermal behavior has been monitored by means of thermal analyses and X-ray powder diffraction. For A being an alkaline metal the decomposition product is a mixture of the sulfates A{sub 2}SO{sub 4} and the dioxides MO{sub 2}, whereas Hg{sub 2}[Ge(S{sub 2}O{sub 7}){sub 3}]Cl{sub 2} shows a more complicated decomposition. The tris-(disulfato)-silicate Na{sub 2}[Si(S{sub 2}O{sub 7}){sub 3}] has additionally been examined by solid state {sup 29}Si and {sup 23}Na NMR spectroscopic measurements. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  15. Distribution of 137Cs in the American Coot (Fulica americana)

    International Nuclear Information System (INIS)

    Potter, C.M.; Brisbin, I.L. Jr.; McDowell, S.G.; Whicker, F.W.

    1989-01-01

    Caesium-137 concentrations were determined for major tissue and organ components of Americal Coots (Fulica americana) wintering on two contaminated reactor cooling reservoirs on the US Department of Energy's Savannah River Plant. Concentrations reflected the relative contamination levels of the two reservoirs. A low ratio of 137 Cs in gut contents to that in muscle indicated that the coots used in the study were established winter residents and tissue 137 Cs had probably reached equilibrium with intake. The contributions of each component to the whole body weight and total 137 Cs body burden were calculated. Skeletal muscle exhibited the highest 137 Cs concentrations and comprised 35% of the total 137 Cs body burden. Gut contents represented 17% of the total body burden. Various other organs were intermediate and bone exhibited the lowest 137 Cs concentrations. Linear regressions were determined for 137 Cs concentrations in skeletal muscle, liver, kidney, gastrointestinal (GI) tract tissue and gut contents, as functions of whole-body concentrations. (author)

  16. Water culture of the rice containing Cs-137

    International Nuclear Information System (INIS)

    Choi, Yong Ho; Keum, Dong Kwon; Lim, Kwang Muk; Jun, In; Park, Doo Won

    2008-10-01

    Pot experiments were carried out in a greenhouse in order to produce Cs-137-containing rice seeds as a source material for use in manufacturing reference rice samples of a high Cs-137 activity. Two kinds of soil were used and two pots were prepared for each kind of soil. Rice plants were water-cultured in the pots and Cs-137 was applied to the surface water to induce a Cs-137 contamination of rice seeds via a plant uptake of Cs-137. Mature rice plants were harvested and Cs-137-containing rice seeds were obtained after some treatment of the harvested plants. These produced rice seeds are going to be provided for the KRISS so as to be used in manufacturing reference rice samples for Cs-137

  17. Mineral surface processes responsible for the decreased retardation (or enhanced mobilization) of 137Cs from HLW tank discharges. 1998 annual progress report

    International Nuclear Information System (INIS)

    Bertsch, P.M.; Zachara, J.M.

    1998-01-01

    'Cesium (137) is a major component of high level weapons waste. At Hanford, single shell tanks (SST''s) with high level wastes (HLW) have leaked supernate containing over 10 6 Ci of 137 Cs and other co-contaminants into the vadose zone. In select locations, 137 Cs has migrated further than expected from retardation experiments and performance assessment calculations. Deep 137 Cs migration has been observed beneath the SX tank farm at Hanford with REDOX wastes as the carrier causing regulatory and stakeholder concern. The causes for expedited migration are unclear. This research is investigating how the sorption chemistry of Cs on Hanford vadose zone sediments changes after contact with solutions characteristic of HLW. The central scientific hypothesis is that the high Na concentration of HLW will suppress surface-exchange reactions of Cs, except those to highly-selective frayed edge sites (FES) of the micaceous fraction. The authors further speculate that the concentrations, ion selectivity, and structural aspects of the FES will change after contact with HLW and that these changes will be manifest in the macroscopic sorption behavior of Cs. The authors believe that migration predictions of Cs can be improved substantially if such changes are understood and quantified. The research has three objectives: (1.) identify how the multi-component surface exchange behavior of Cs on Hanford sediments changes after contact with HLW simulants that span a range of relevant chemical (Na, OH, Al, K) and temperature conditions (23-80 C); (2) reconcile changes in sorption chemistry with microscopic and molecular changes in site distribution, chemistry, mineralogy, and surface structure of the micaceous fraction; (3) integrate mass-action-solution exchange measurements with changes in the structure/site distribution of the micaceous fraction to yield a multicomponent exchange model relevant to high ionic strength and hydroxide for prediction of environmental Cs sorption.'

  18. 133Cs NMR investigation of 2D frustrated Heisenberg antiferromagnet, Cs2CuCl4

    Science.gov (United States)

    Vachon, M.-A.; Kundhikanjana, W.; Straub, A.; Mitrovic, V. F.; Reyes, A. P.; Kuhns, P.; Coldea, R.; Tylczynski, Z.

    2006-10-01

    We report 133Cs nuclear magnetic resonance (NMR) measurements on the 2D frustrated Heisenberg antiferromagnet Cs2CuCl4 down to 2 K and up to 15 T. We show that 133Cs NMR is a good probe of the magnetic degrees of freedom in this material. Cu spin degrees of freedom are sensed through a strong anisotropic hyperfine coupling. The spin excitation gap opens above the critical saturation field. The gap value was determined from the activation energy of the nuclear spin-lattice relaxation rate in a magnetic field applied parallel to the Cu chains (\\skew3\\hat{b} axis). The values of the g-factor and the saturation field are consistent with the neutron-scattering and magnetization results. The measurements of the spin spin relaxation time are exploited to show that no structural changes occur down to the lowest temperatures investigated.

  19. Sorption of Fe3+ , Co2+ , Ce3+ , Cs+ and Ba2+ in zeolite X

    International Nuclear Information System (INIS)

    Martinez M, V.

    1994-01-01

    The sorption behavior of Fe 3+ , Co 2+ , Ce 3+ , Cs + , and Ba 2+ in aqueous solutions, was studied in presence of zeolite X. Solutions of Fe(NO 3 ) 3 . 9 H 2 O, Co(NO 3 ) 2 . 6 H 2 O, Ce(NO 3 ) 3 . 6 H 2 O, Cs NO 3 and Ba(NO 3 ) 2 were labelled with the respectively radioactive isotopes Fe 59 , Co 60 , Cs 134 , Ba 139 and Ce 141 . 20 ml. of each solution was left in contact with 200 mg. of zeolite for different periods. Later the zeolites were separated by centrifugation from the aqueous solutions and the radioactivity of the aqueous phases was measured with a NaI(Tl) solid-state well detector coupled to a single-channel Picker analyzer or with a Gel hyper pure solid-state detector coupled to a 2048 channel pulse height analyzer. When Cs + in the aqueous solutions was left in contact with zeolite X it was found that it does not occupy all cationic sites in the zeolite due to the ionic radium effect. A similar behavior was found for the divalent ions. In all cases, when the pH was not controlled, the zeolite lost part of its crystallinity and when the divalent ions were exchanged again by Na + , the zeolite recovered completely its crystallinity. During the sorption, the ionic radius, and the charge are important parameters as well as the pH. When the pH of the solution was adjusted between 6.5 - 7.0 the crystallinity was maintained in some cases. For Fe 3+ the crystallinity after the ion exchange was 94 % and when the pH was not adjusted the crystallinity was completely lost. It was found as well that the zeolite X induces the formation of H 3 O + which competes with the cations for the sites in the zeolite. (Author)

  20. Foundation Flash CS4 for Designers

    CERN Document Server

    Green, Tom

    2008-01-01

    In this book, you'll learn:* How to create effective animations using the new Motion Editor and animation tools * How to use the new 3D features to animate objects in 3D space * Best-practice tips and techniques from some of the top Flash practitioners on the planet * How to create captioned video and full-screen video, and deploy HD video using Flash * Techniques for using the Flash UI components as well as XML documents to create stunning,interactive presentations If you're a Flash designer looking for a solid overview of Flash CS4, this book is for you. Through the use of solid and practica

  1. Reactor Configuration Development for ARIES-CS

    International Nuclear Information System (INIS)

    Ku LP

    2005-01-01

    New compact, quasi-axially symmetric stellarator configurations have been developed as part of the ARIES-CS reactor studies. These new configurations have good plasma confinement and transport properties, including low losses of α particles and good integrity of flux surfaces at high β. We summarize the recent progress by showcasing two attractive classes of configurations--configurations with judiciously chosen rotational transforms to avoid undesirable effects of low order resonances on the flux surface integrity and configurations with very small aspect ratios (∼2.5) that have excellent quasi-axisymmetry and low field ripples

  2. 137Cs - Brachytherapy sources : a technology scenario

    International Nuclear Information System (INIS)

    Varma, R.N.

    2001-01-01

    Cancer has emerged as one of the major cause of morbidity and mortality all over the world. India houses world's second largest population and registers 4-5 lakhs new cancer cases every year. Cancer of cervix is most common form of malignancy among Indian women. Radiation therapy, especially intracavity brachytherapy in conjunction with other modalities like surgery, chemotherapy has been found to be highly effective for the management and control of cervical carcinoma at all stages. A technology has been developed indigenously for the fabrication of 137 Cs sources for brachytherapy applications

  3. Dreamweaver CS55 The Missing Manual

    CERN Document Server

    McFarland, David

    2011-01-01

    Dreamweaver is the tool most widely used for designing and managing professional-looking websites, but it's a complex program. That's where Dreamweaver CS5.5: The Missing Manual comes in. With its jargon-free explanations, 13 hands-on tutorials, and savvy advice from Dreamweaver expert Dave McFarland, you'll master this versatile program with ease. Get A to Z guidance. Go from building your first web page to creating interactive, database-driven sites.Build skills as you learn. Apply your knowledge through tutorials and downloadable practice files.Create a state-of-the-art website. Use powerf

  4. Adobe Photoshop CS5 for photographers

    CERN Document Server

    Evening, Martin

    2010-01-01

    With the new edition of this proven bestseller, Photoshop users can master the power of Photoshop CS5 with internationally renowned photographer and Photoshop hall-of-famer Martin Evening by their side.  In this acclaimed reference work, Martin covers everything from the core aspects of working in Photoshop to advanced techniques for professional results. Subjects covered include organizing a digital workflow, improving creativity, output, automating Photoshop, and using Camera RAW. The style of the book is extremely clear, with real examples, diagrams, illustrations, and step-by-step ex

  5. Flash CS5 The Missing Manual

    CERN Document Server

    Grover, Chris

    2010-01-01

    Once you know how to use Flash, you can create everything from simple animations to high-end desktop applications, but it's a complex tool that can be difficult to master on your own-unless you have this Missing Manual. This book will help you learn all you need to know about Flash CS5 to create animations that bring your ideas to life. Learn animation basics. Find everything you need to know to get started with FlashMaster the Flash tools. Learn the animation and effects toolset, with clear explanations and hands-on examplesUse 3D effects. Rotate and put objects in motion in three dimensions

  6. 137CS in cod from Barents sea

    International Nuclear Information System (INIS)

    Kellermann, H.-J.; Kanisch, G.; Krueger, A.

    2003-01-01

    After publication of the Yablovkov report about dumping of radioactive waste by the former Soviet Union the Institute for Fishery Ecology has analysed fish from Barents Sea for radioactivity. In all studies 137 Cs concentrations in cod fillet showed a clear dependance from fish length. Results from an analysis of covariance for cod of 70 cm length have minor changes within Barents Sea and indicate a rapid decay to a value as is expected for marine fish which is only influenced by global fallout. (orig.)

  7. Foundation Flash CS5 for Designers

    CERN Document Server

    Green, T

    2010-01-01

    Flash is one of the most engaging, innovative, and versatile technologies available - allowing the creation of anything from animated banners and simple cartoons to Rich Internet Applications, interactive videos, and dynamic user interfaces for web sites, kiosks, devices, or DVDs. The possibilities are endless, and now it just got better. Flash CS5 boasts a host of new features, including better support for mobile devices, a whole new animation engine enabling full manipulation of tweens and paths, custom easing, improved inverse kinematics, a revamped timeline, built-in 3D, and much more. Thi

  8. Hydrolysis of Rice Straw Pretreated by Na2SO3 Over Fe-resin/NaCl

    Directory of Open Access Journals (Sweden)

    YANG Hui

    2017-05-01

    Full Text Available To increase the conversion of rice straw(RS and the yield of products, we employed three methods, which were ultrasonic wave, steam explosion and Na2SO3 pretreatment to pretreat RS(the treated RS noted as CS-RS, ZQ-RS and Na2SO3-RS, respectively and found that Na2SO3 treatment was the best pretreatment method based on XRD, SEM, elemental analysis and content of cellulose, hemicellulose and lignin. The conversion of Na2SO3-RS and the yield of total reducing sugar(TRS and levulinic acid(LA were 97.3%, 29.6% and 13.5%, respectively by 10% Fe-resin in 3.3% NaCl solution under 200 ℃.

  9. Hybridization of Single Nanocrystals of Cs4PbBr6 and CsPbBr3.

    Science.gov (United States)

    Weerd, Chris de; Lin, Junhao; Gomez, Leyre; Fujiwara, Yasufumi; Suenaga, Kazutomo; Gregorkiewicz, Tom

    2017-09-07

    Nanocrystals of all-inorganic cesium lead halide perovskites (CsPbX 3 , X = Cl, Br, I) feature high absorption and efficient narrow-band emission which renders them promising for future generation of photovoltaic and optoelectronic devices. Colloidal ensembles of these nanocrystals can be conveniently prepared by chemical synthesis. However, in the case of CsPbBr 3 , its synthesis can also yield nanocrystals of Cs 4 PbBr 6 and the properties of the two are easily confused. Here, we investigate in detail the optical characteristics of simultaneously synthesized green-emitting CsPbBr 3 and insulating Cs 4 PbBr 6 nanocrystals. We demonstrate that, in this case, the two materials inevitably hybridize, forming nanoparticles with a spherical shape. The actual amount of these Cs 4 PbBr 6 nanocrystals and nanohybrids increases for synthesis at lower temperatures, i.e., the condition typically used for the development of perovskite CsPbBr 3 nanocrystals with smaller sizes. We use state-of-the-art electron energy loss spectroscopy to characterize nanoparticles at the single object level. This method allows distinguishing between optical characteristics of a pure Cs 4 PbBr 6 and CsPbBr 3 nanocrystal and their nanohybrid. In this way, we resolve some of the recent misconceptions concerning possible visible absorption and emission of Cs 4 PbBr 6 . Our method provides detailed structural characterization, and combined with modeling, we conclusively identify the nanospheres as CsPbBr 3 /Cs 4 PbBr 6 hybrids. We show that the two phases are independent of each other's presence and merge symbiotically. Herein, the optical characteristics of the parent materials are preserved, allowing for an increased absorption in the UV due to Cs 4 PbBr 6 , accompanied by the distinctive efficient green emission resulting from CsPbBr 3 .

  10. Luminescent CsPbI.sub.3./sub. and Cs.sub.4./sub.PbI.sub.6./sub. aggregates in annealed CsI:Pb crystals

    Czech Academy of Sciences Publication Activity Database

    Babin, V.; Fabeni, P.; Nikl, Martin; Nitsch, Karel; Pazzi, G.P.; Zazubovich, S.

    2001-01-01

    Roč. 226, č. 2 (2001), s. 419-428 ISSN 0370-1972 Institutional research plan: CEZ:AV0Z1010914 Keywords : CsPbI 3 * Cs 4 PbI 6 * nanoaggregates * luminescence Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 0.873, year: 2001

  11. Mobility of 137Cs in freshwater lakes: A mass balance and diffusion study of Lake St. Clair, Southeast Michigan, USA

    Science.gov (United States)

    Wang, Jinlong; Baskaran, Mark; Niedermiller, John

    2017-12-01

    Cesium-137 is one of the most widely utilized anthropogenic radionuclides, both as a tracer and chronometer in the environment. Its application as an effective chronometer requires a thorough understanding of its geochemical behavior in aqueous systems. In this study, we collected and analyzed a suite of time-series water samples over a period of 8 months (April - November 2015), for particulate and dissolved 137Cs activities from a watershed in southeast Michigan, USA, using Cu2Fe(CN)6-coated cartridges developed to pre-concentrate dissolved 137Cs. We also conducted a series of laboratory experiments with the natural freshwater sediment samples and water with different chemical composition. There were seasonal variations of both particulate and dissolved 137Cs activities in the watersheds of Lake St. Clair. The distribution coefficients of 137Cs determined over a period of 8 months varied between 0.14 × 105 and 6.1 × 105 mL g-1 (mean: 2.9 × 105 mL g-1). The annual input and export flux of total 137Cs activity via rivers into and out of Lake St. Clair were calculated to be 3.6 × 1010 Bq and 1.6 × 1010 Bq, respectively. The amount of 137Cs derived by diffusion from interstitial pore water to the water column was estimated to be 0.30 × 1010 Bq (8.3% of the total input flux) which is similar to the percentage of 137Cs desorption (13%-20%) from sediment placed in oxic soft water system over a period of 30-106 days. For the same concentrations of NH4+, Mn2+, K+, Mg2+, Ca2+, Na+ and Sr2+ in a distilled water, our lab work showed that the sediment-sorbed 137Cs is displaced by ions in the order NH4+ > Mn2+ > K+ > Mg2+ ≈ Ca2+ > Na+ > Sr2+. In laboratory studies, 137Cs sorbed onto sediment was found to be less mobile in oxic soft water (Kd: 2.0 × 103 mL g-1) and more mobile in anoxic soft water (Kd: 0.2 × 103 mL g-1). In a hard water system, however, there is no significant difference in Kd values for both oxic and anoxic conditions. The sequence of Kd values is

  12. Scintillation response of CsI: Tl crystal under neutron, gamma, alpha particles and beta excitations

    Energy Technology Data Exchange (ETDEWEB)

    Pereira, Maria da Conceicao Costa; Madi Filho, Tufic; Lopes, Valdir Maciel; Berretta, Jose Roberto; Cardenas, Jose Patricio Nahuel, E-mail: macoper@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2015-07-01

    Among the converters of X and gamma radiation in light photons, known as scintillators, the one which is the most efficient emits photons with a wavelength near 400 nm. Particularly, among them, the cesium iodine doped with thallium (CsI:Tl) crystal is that which matches better between the light emission spectrum (peak at 540 nm) and the quantum sensitivity curve of the photodiodes and CCD (Charge Coupled Device). This explains the renewed interest in using this crystal as scintillator. Although the CsI:Tl crystal is commercially available, its local development would give the possibility to obtain it in different geometric configurations and coupling. Moreover, there is a special interest in studying new conditions that will alter the properties of this crystal in order to achieve a optimal level of its functional characteristics. Having an efficient national scintillator with low cost is a strategic opportunity to study the response of a detector applied to different types of radiation. The crystal of cesium iodide activated with thallium (CsI:Tl) has a high gamma detection efficiency per unit volume. In this paper, the CsI:Tl crystal, grown by the vertical Bridgman technique in evacuated silica ampoules and with the purpose of use as radiation detectors, is described. To evaluate the scintillator, measures of the thallium distribution in the crystal volume were taken, with overall efficiency score. The scintillator response was studied through gamma radiation from sources of {sup 137}Cs, {sup 60}Co, {sup 22}Na, {sup 54}Mn, {sup 131}I and {sup 99m}Tc; the beta radiation from source of {sup 90}Sr/{sup 90}Y, alpha particles from {sup 241}Am source and the scintillator response to neutrons from Am/Be source. The energetic resolution for {sup 137}Cs gamma rays (662 keV) was 10%. The results showed the validity of using the CsI:Tl crystal developed in our laboratory, in many applications in the area of radiation detectors. (author)

  13. Photodissociation of CS from Excited Rovibrational Levels

    Science.gov (United States)

    Pattillo, R. J.; Cieszewski, R.; Stancil, P. C.; Forrey, R. C.; Babb, J. F.; McCann, J. F.; McLaughlin, B. M.

    2018-05-01

    Accurate photodissociation cross sections have been computed for transitions from the X 1Σ+ ground electronic state of CS to six low-lying excited electronic states. New ab initio potential curves and transition dipole moment functions have been obtained for these computations using the multi-reference configuration interaction approach with the Davidson correction (MRCI+Q) and aug-cc-pV6Z basis sets. State-resolved cross sections have been computed for transitions from nearly the full range of rovibrational levels of the X 1Σ+ state and for photon wavelengths ranging from 500 Å to threshold. Destruction of CS via predissociation in highly excited electronic states originating from the rovibrational ground state is found to be unimportant. Photodissociation cross sections are presented for temperatures in the range between 1000 and 10,000 K, where a Boltzmann distribution of initial rovibrational levels is assumed. Applications of the current computations to various astrophysical environments are briefly discussed focusing on photodissociation rates due to the standard interstellar and blackbody radiation fields.

  14. The radiation chemistry of the Cs-7SB modifier used in Cs and Sr extraction

    International Nuclear Information System (INIS)

    Swancutt, Katy L.; Cullen, Thomas D.; Mezyk, Stephen P.; Elias, Gracy; Bauer, William F.; Peterman, Dean R.; Riddle, Catherine L.; Ball, R. Duane; Mincher, Bruce J.; Muller, James J.

    2011-01-01

    The compound 1-(2,2,3,3,-tetrafluoropropoxy)-3-(4-sec-butylphenoxy)-2-propanol, also called Cs-7SB, is used as a solvent modifier in formulations containing calixarenes and crown ethers for cesium and/or strontium extraction from nuclear waste solutions. The compound solvates complexes of both metals and concentration decreases result in lowered extraction efficiency for both. The use of Cs-7SB in nuclear solvent extraction ensures that it will be exposed to high radiation doses, and thus its radiation chemical robustness is a matter of interest in the design of extraction systems employing it. The behavior of the compound in irradiated solution, both in the presence and absence of a nitric acid aqueous phase was investigated here using steady state and pulsed radiolysis techniques. The rate constants for the aqueous reactions of Cs-7SB with H, OH, NO 3 and NO 2 radicals are reported. UPLC-UV-MS results were used to identify major products of the radiolysis of Cs-7SB in contact with nitric acid, and revealed the production of hydroxylated nitro-derivatives. Reaction mechanisms are proposed and it is concluded that the aryl ether configuration of this molecule makes it especially susceptible to nitration in the presence of radiolytically-produced nitrous acid. Fluoride yields are also given under various conditions.

  15. Postsynthesis Transformation of Insulating Cs4PbBr6 Nanocrystals into Bright Perovskite CsPbBr3 through Physical and Chemical Extraction of CsBr.

    Science.gov (United States)

    Palazon, Francisco; Urso, Carmine; De Trizio, Luca; Akkerman, Quinten; Marras, Sergio; Locardi, Federico; Nelli, Ilaria; Ferretti, Maurizio; Prato, Mirko; Manna, Liberato

    2017-10-13

    Perovskite-related Cs 4 PbBr 6 nanocrystals present a "zero-dimensional" crystalline structure where adjacent [PbBr 6 ] 4- octahedra do not share any corners. We show in this work that these nanocrystals can be converted into "three-dimensional" CsPbBr 3 perovskites by extraction of CsBr. This conversion drastically changes the optoelectronic properties of the nanocrystals that become highly photoluminescent. The extraction of CsBr can be achieved either by thermal annealing (physical approach) or by chemical reaction with Prussian Blue (chemical approach). The former approach can be simply carried out on a dried film without addition of any chemicals but does not yield a full transformation. Instead, reaction with Prussian Blue in solution achieves a full transformation into the perovskite phase. This transformation was also verified on the iodide counterpart (Cs 4 PbI 6 ).

  16. Transfer of Chernobyl-derived 134Cs, 137Cs, 131I and 103Ru from flowers to honey and pollen

    International Nuclear Information System (INIS)

    Bunzl, K.; Kracke, W.

    1988-01-01

    The activity concentrations of 137 Cs, 134 Cs, 131 I and 103 Ru were determined separately in honey and pollen samples collected from a single bee colony during several months after the deposition of Chernobyl fallout. The source of each honey and pollen sample was determined by pollen analysis. Although the activity concentrations in honey and pollen varied with time, the concentrations of 137 Cs and 134 Cs were, in general, higher in pollen than in honey. For 103 Ru and 131 I, these differences were comparatively small. The mean 131 I/ 137 Cs and 103 Ru/ 137 Cs ratios were about one order of magnitude higher in honey than in pollen. The mean 131 I/ 103 Ru ratio was about the same for honey and pollen. This observation, in the light of the corresponding nuclide ratios found in the deposition, suggests that 137 Cs, 134 Cs, 131 I and 103 Ru were taken up by the plant leaves and transported to nectar and pollen. The higher activity concentrations of 137 Cs and 134 Cs in pollen, relative to honey, indicate that these radionuclides behave analogously to potassium, which is also found in higher quantities in pollen. (author)

  17. The behavior of radioactive 137Cs and stable Cs at the isolated undisturbed mountain pond in Fukui, Japan

    International Nuclear Information System (INIS)

    Iwamoto, Kazumi; Kimura, Makio; Ando, Kenji; Amano, Hikaru

    2003-01-01

    The behavior of radioactive 137 Cs and stable Cs at the isolated undisturbed mountain pond in Fukui, Japan was studied for the pond water, the sedimentary grains and the soil near the pond. The concentrations of 137 Cs and stable Cs in the pond water ranged from 0.23 to 0.85 Bq/m 3 and from 0.005 to 0.018 mg/m 3 , respectively. The sedimentary grains were sorted by sieving into fractions with diameter from 2 mm to less than 38 μm. The concentrations of 137 Cs and stable Cs in the sorted grains were measured, and those of the adsorbed state were determined by subtracting the concentration of the grain matrix. The adsorbed concentrations increased with decrease in particle diameter and depended less on the kind of samples. The in-situ distribution coefficient Kd depended largely on particle diameter and increased with the decrease in diameter. The values of Kd ranged from about 20 to 1200 m 3 /kg for stable Cs and about 15 to 1000 m 3 /kg for 137 Cs, and the Kd of 137 Cs seemed to be slightly smaller than that of stable Cs. The concentration of stable Cs in the sedimentary mud was found to be close to that of the fine grains. The concentrations of stable Cs in the soil near the pond was about 7.7 mg/kg, and that of 137 Cs was about 0.6 kBq/kg for the surface layer soil and decreased with increase in soil depth. (author)

  18. Tunable CsPbBr3/Cs4PbBr6 phase transformation and their optical spectroscopic properties.

    Science.gov (United States)

    Chen, Xiao; Chen, Daqin; Li, Junni; Fang, Gaoliang; Sheng, Hongchao; Zhong, Jiasong

    2018-04-24

    As a novel type of promising materials, metal halide perovskites are a rising star in the field of optoelectronics. On this basis, a new frontier of zero-dimensional perovskite-related Cs4PbBr6 with bright green emission and high stability has attracted an enormous amount of attention, even though its photoluminescence still requires to clarification. Herein, the controllable phase transformation between three-dimensional CsPbBr3 and zero-dimensional Cs4PbBr6 is easily achieved in a facile ligand-assisted supersaturated recrystallization synthesis procedure via tuning the amount of surfactants, and their unique optical properties are investigated and compared in detail. Both Cs4PbBr6 and CsPbBr3 produce remarkably intense green luminescence with quantum yields up to 45% and 80%, respectively; however, significantly different emitting behaviors are observed. The fluorescence lifetime of Cs4PbBr6 is much longer than that of CsPbBr3, and photo-blinking is easily detected in the Cs4PbBr6 product, proving that the zero-dimensional Cs4PbBr6 is indeed a highly luminescent perovskite-related material. Additionally, for the first time, tunable emissions over the visible-light spectral region are demonstrated to be achievable via halogen composition modulations in the Cs4PbX6 (X = Cl, Br, I) samples. Our study brings a simple method for the phase control of CsPbBr3/Cs4PbBr6 and demonstrates the intrinsic luminescence nature of the zero-dimensional perovskite-related Cs4PbX6 products.

  19. Influence of time, temperature, pH and inhibitors on bioaccumulation of radiocaesium - 137Cs by lichen Hypogymnia physodes

    International Nuclear Information System (INIS)

    Pipiska, M.; Kociova, M.; Hornik, M.; Augustin, J.; Lesny, J.

    2005-01-01

    Caesium bioaccumulation experiments were carried out at 4 to 60 o C using natural samples of the lichen Hypogymnia physodes. Thalli were incubated in 2.5 μmol.l -1 CsCl solutions labelled with 137 CsCl for up to 24 h at pH values from 2 to 10. Bioaccumulation of Cs + ions in the first phase of the lichen-CsCl solution interaction is rapid, neither pH, nor temperature dependent within the range 4 to 60 o C and observed also with the lichen biomass thermally inactivated at 60 o C or chemically by formaldehyde. The second phase of 137 Cs bioaccumulation is time, temperature and pH dependent and is inhibited by formaldehyde and thermal inactivation. The process at the initial concentration C 0 = 2.5 μmol.l -1 CsCl and 20 o C reached equilibrium within 12 hours. It can be described by the first order reaction kinetics equation: log [C t ] = 1.89 - 0.00153 t, R = -0.950. Maximal values of Cs-bioaccumulation were observed at 20 o C with minimum at 4 o C and 40 o C and at pH 4-5 with minimum at pH 2 and pH 6. Low caesium efflux values from lichen thalli by water and 0.1 mol.l -1 neutral salts at 20 o C and 24 h equilibrium were observed. Efflux characterized by distribution coefficients D = [Cs] solution /[Cs] biomass at biomass/solution ratio 1:25 (w/v, wet wt.), decreases in the order: Li+ - 78 · 10 -3 > NH 4 + = K + - 15 · 10 -3 > Cs + = Na + - 11 · 10 -3 . Low extractability of caesium from lichen by water and salt solutions can explain long persistent times of radiocaesium contamination sorbed by lichens, observed by many authors in caesium contaminated forest and mountain regions. Hypothesis of the role of the lichen secondary metabolites as caesium binders is discussed. (author)

  20. A first attempt to derive soil erosion rates from 137Cs airborne gamma measurements in two Alpine valleys

    Science.gov (United States)

    Arata, Laura; Meusburger, Katrin; Bucher, Benno; Mabit, Lionel; Alewell, Christine

    2016-04-01

    The application of fallout radionuclides (FRNs) as soil tracers is currently one of the most promising and effective approach for evaluating soil erosion magnitudes in mountainous grasslands. Conventional assessment or measurement methods are laborious and constrained by the topographic and climatic conditions of the Alps. The 137Cs (half-life = 30.2 years) is the most frequently used FRN to study soil redistribution. However the application of 137Cs in alpine grasslands is compromised by the high heterogeneity of the fallout due to the origin of 137Cs fallout in the Alps, which is linked to single rain events occurring just after the Chernobyl accident when most of the Alpine soils were still covered by snow. The aim of this study was to improve our understanding of the 137Cs distribution in two study areas in the Central Swiss Alps: the Ursern valley (Canton Uri), and the Piora valley (Canton Ticino). In June 2015, a helicopter equipped with a NaI gamma detector flew over the two study sites and screened the 137Cs activity of the top soil. The use of airborne gamma measurements is particularly efficient in case of higher 137Cs concentration in the soil. Due to their high altitude and high precipitation rates, the Swiss Alps are expected to be more contaminated by 137Cs fallout than other parts of Switzerland. The airborne gamma measurements have been related to several key parameters which characterize the areas, such as soil properties, slopes, expositions and land uses. The ground truthing of the airborne measurements (i.e. the 137Cs laboratory measurements of the soil samples collected at the same points) returned a good fit. The obtained results offer an overview of the 137Cs concentration in the study areas, which allowed us to identify suitable reference sites, and to analyse the relationship between the 137Cs distribution and the above cited parameters. The authors also derived a preliminary qualitative and a quantitative assessment of soil redistribution

  1. Pulsed Cs beam development for the BNL polarized H- source

    International Nuclear Information System (INIS)

    Alessi, J.G.

    1983-01-01

    A pulsed Cs + beam has been developed for use on a polarized H - source. Cesium ion production is by surface ionization using a porous tungsten ionizer. While satisfactory current pulses (5 to 10 mA greater than or equal to 0.5 ms) can be obtained, the pulse shapes are a sensitive function of the ionizer temperature and Cs surface coverage. The beam optical requirements are stringent, and the optics have been studied experimentally for both Cs + and Cs 0 beams. Computer calculations are in good agreement with the observed results. The present source has delivered 2.6 mA of Cs + through the interaction region of the polarized ion source, and as much as 2.0 particle mA of Cs 0 . A new source is being built which is designed to give 15 mA through the interaction region

  2. Absolute measurement of the desintegration rate of 137 Cs by 4Π (BS) e--X coincidence method

    International Nuclear Information System (INIS)

    Koskinas, M.F.; Dias, M.S.

    1989-01-01

    The method developed by the Nuclear Metrology Laboratory for the absolute measurement of the desintegration rate of 137 Cs by 4Π(BS)e - -X is described. The conversion electron are measured by a pair of surface barrier detectors with 200mm 2 of active area and 1000μm of depletion depth. The X-rays are measured by two 50.8mm diameter and 1.0mm thick NaI (Tl) scintillation counters. (author) [pt

  3. Dynamic modelling of Cs-137 contamination in Denmark

    International Nuclear Information System (INIS)

    Oehlenschlaeger, M.

    1989-01-01

    The paper describes the structure of a dynamic food-chain transport model for Cs-137 in the Danish terrestrial environment. The model solves a set of linear, coupled differential equations in order to estimate the inventories and concentrations of Cs-137 in the soil, vegetation, animal tissue and animal product as a function of time based on the Cs-137 concentrations in the air after an accidental release. Meteorological conditions and seasonal variations in agricultural practice are included. (orig.)

  4. Uptake of Cs 137 from farmland 1986-1989

    International Nuclear Information System (INIS)

    Holmberg, M.

    1986-12-01

    The basic mechanisms of the accumulation of Cs 137 in grass, corn, oleiferous plants, potatoes etc are described. It is also presented as a function of time after the deposition. Transport of Cs 137 to milk, meat and bacon is described. A prognosis of Cs 137 in food products for the coming two years is made on basis of the estimated data. (G.B.)

  5. Evaluation of caesium atomic fountain NICT-CsF1

    International Nuclear Information System (INIS)

    Kumagai, M.; Ito, H.; Kajita, M.; Hosokawa, M.

    2008-01-01

    In this paper, we describe the first caesium atomic fountain primary frequency standard NICT-CsF1 of National Institute of Information Communications Technology (NICT) in Tokyo, Japan. The structure of the NICT-CsF1 system and evaluation procedure of the systematic frequency shifts and their uncertainties are presented. Typically, NICT-CsF1 has a frequency stability of 4 * 10 -13 /τ 1/2 and a frequency uncertainty of 1.9 * 10 -15 . (authors)

  6. 137Cs in man due to nuclear fallout

    International Nuclear Information System (INIS)

    Poulheim, K.F.

    1981-01-01

    137 Cs has been determined in man with the aid of a whole-body counter. It is shown that the specific 137 Cs content (as related to the potassium content in man) continuously decreased from 1965 through 1974. After a slight increase in 1975, possibly caused by a Chinese atmospheric nuclear test in June 1974, the 137 Cs content again decreased in the following years. (author)

  7. Study of the functional characteristics of a NaI(Tl) scintillator gamma spectrometer

    International Nuclear Information System (INIS)

    Jesus Barbosa, S. de.

    1983-01-01

    Functional characteristics (resolution, stability, linearity, counting efficiency) of a NaI(Tl) scintillator gamma spectrometer were studied. Diagrams were plotted and several standard sources ( 241 Am, 109 Cd, 57 Co, 137 Cs, 54 Mn, 22 Na) with gamma energies ranging from 60 to 1275 KeV were used. (C.L.B.) [pt

  8. Behaviour of 134Cs in the aquatic ecosystems

    International Nuclear Information System (INIS)

    Xu Yinliang; Chen Chuanqun

    1992-07-01

    The diminution of 134 Cs in the aquatic phases and the absorption of 134 Cs by aquatic lives observe the exponential expression. i.e. Y Ae be . The relationships between the enrichment factor of 134 Cs(K) and the time(t) in the aquatic lives can be represented by a linear equation, K A + Bt. The value of K in the Alternanthera philoxeroides was about 560. That can be used for monitoring and purifying the water phase contaminated by 134 Cs. Fish can absorb 134 Cs from water phase and store it in liver and kidney. The specific activity of 134 Cs in fish flesh was low but the percentage of radioactivity was high that was about 30% of total radioactivity in the fish. River mud can strongly absorb 134 Cs and reduce the absorption by aquatic lives. It is a good adsorbent and purifying agent with low cost for treatment of 134 Cs. The K + can prevent aquatic lives from absorbing Cs + because of antagonistic function

  9. Initial interaction of {sup 137}Cs with soils

    Energy Technology Data Exchange (ETDEWEB)

    Nagasaki, S., E-mail: nagasaki@mcmaster.ca [McMaster Univ., Hamilton, Ontario (Canada); Makino, H.; Saito, T. [Univ. of Toyko, Tokyo (Japan)

    2013-07-01

    It is critical to understand the physicochemical behaviour of Cs in soil in order to progress the decontamination of soils which were contaminated by nuclear power plant accident and to improve the reliability of safety assessment of used nuclear fuel disposal. In this paper, the initial interactions of {sup 137}Cs with soils, which were sampled in Fukushima 38 days after Fukushima Accident, were investigated with sequential extraction method. It was found that there were fast and slow processes of fixation of {sup 137}Cs in clay minerals and that the organic substances might play an important role on kinetics of {sup 137}Cs in soils. (author)

  10. Behaviour of {sup 137} Cs in oxysoils and Goiania soil

    Energy Technology Data Exchange (ETDEWEB)

    Wassermann, Maria Angelica [Instituto de Radioprotecao e Dosimetria (IRD), Rio de Janeiro, RJ (Brazil)

    1997-12-31

    {sup 137} Cs soil-to-plant transfer factor obtained in oxy soils accidentally contaminated in Goiania and artificially contaminated shows that these soils present higher transfer when compared with data obtained under temperate climates. These differences were discussed in the light of pedology and geochemical partitioning. Some tropical soil characteristics as acidity, low available nutritive elements and low content of 2:1 clay type seems determine high availability for {sup 137} Cs. Results of sequential extraction showed {sup 137} Cs weakly bound to soil components and underline the importance of Fe oxides in the control of {sup 137} Cs availability in tropical climates. (author) 25 refs., 2 figs., 2 tabs.

  11. Fractionation of (137)Cs and Pu in natural peatland.

    Science.gov (United States)

    Mihalík, Ján; Bartusková, Miluše; Hölgye, Zoltán; Ježková, Tereza; Henych, Ondřej

    2014-08-01

    High Cs-137 concentrations in plants growing on peatland inspired us to investigate the quantity of its bioavailable fraction in natural peat. Our investigation aims to: a) estimate the quantity of bioavailable Cs-137 and Pu present in peat, b) verify the similarity of Cs-137 and K-40 behaviours, and c) perform a quantification of Cs-137 and Pu transfer from peat to plants. We analysed the vertical distribution of Cs-137 and Pu isotopes in the peat and their concentrations in plants growing on these places. Bioavailability of radionuclides was investigated by sequential extraction. Sequential analyses revealed that it was the upper layer which contained the majority of Cs-137 in an available form while deeper layers retained Cs-137 in immobile fractions. We can conclude that 18% of all Cs-137 in the peat is still bioavailable. Despite of the low quantity of bioavailable fraction of Cs-137 its transfer factor reached extremely high values. In the case of Pu, 64% of its total amount was associated with fulvic/humic acids which resulted in the high transfer factor from peat to plants. 27 years after the Chernobyl nuclear accident, the significant part of radionuclides deposited in peatland is still bioavailable. Copyright © 2014 Elsevier Ltd. All rights reserved.

  12. Effect of nutrition peculiarities on 137Cs uptake

    International Nuclear Information System (INIS)

    Knizhnikov, V.A.; Marej, A.N.; Borisov, B.K.; Petukhova, Eh.V.

    1980-01-01

    Reasons for different 137 Cs uptake from diets of the vegetable-animal type are studied. Indexes of accumulation multiplicity for Moscow and the Byelorussian-Ukrainian wooded district are compared. 137 Cs buildup levels in the organism of the USSR and the USA population are presented. The most probable reason for peculiarities in 137 Cs uptake from various types of diet, as well as the reason for the alterations in the uptake of this radionuclide from the diet of the same type, is the non-uniformity of 137 Cs contribution of aerial and nonaerial origin

  13. Modelling 137Cs uptake in plants from undisturbed soil monoliths

    International Nuclear Information System (INIS)

    Waegeneers, Nadia; Smolders, Erik; Merckx, Roel

    2005-01-01

    A model predicting 137 Cs uptake in plants was applied on data from artificially contaminated lysimeters. The lysimeter data involve three different crops (beans, ryegrass and lettuce) grown on five different soils between 3 and 5 years after contamination and where soil solution composition was monitored. The mechanistic model predicts plant uptake of 137 Cs from soil solution composition. Predicted K concentrations in the rhizosphere were up to 50-fold below that in the bulk soil solution whereas corresponding 137 Cs concentration gradients were always less pronounced. Predictions of crop 137 Cs content based on rhizosphere soil solution compositions were generally closer to observations than those based on bulk soil solution composition. The model explained 17% (beans) to 91% (lettuce) of the variation in 137 Cs activity concentrations in the plants. The model failed to predict the 137 Cs activity concentration in ryegrass where uptake of the 5-year-old 137 Cs from 3 soils was about 40-fold larger than predicted. The model generally underpredicted crop 137 Cs concentrations at soil solution K concentration below about 1.0 mM. It is concluded that 137 Cs uptake can be predicted from the soil solution composition at adequate K nutrition but that significant uncertainties remain when soil solution K is below 1 mM

  14. Cs separation from nitric acid solutions of radioactive waste

    International Nuclear Information System (INIS)

    Heckmann, K.; Pieronczyk, W.; Strnad, J.; Feldmaier, F.

    1989-01-01

    It was the objective of this study to selectively separate active caesium (Cs-134 and Cs-137) from acid radioactive waste solutions (especially MAW and HAWC). The following 'strategy' was designed for a separation process: synthesis of reagents which are acid-resistant and selective for caesium; precipitation of Cs + and separation of the precipitates by filtration or centrifugation or precipitation of Cs + and separation of the precipitates by flotation; caesium separation by liquid-liquid extraction. As precipitating agents, sodium tetraphenylborate (kalignost) and several of its fluorine derivatives were examined. (orig./RB) [de

  15. Microhydration of caesium compounds: Cs, CsOH, CsI and Cs₂I₂ complexes with one to three H₂O molecules of nuclear safety interest.

    Science.gov (United States)

    Sudolská, Mária; Cantrel, Laurent; Cernušák, Ivan

    2014-04-01

    Structure and thermodynamic properties (standard enthalpies of formation and Gibbs free energies) of hydrated caesium species of nuclear safety interest, Cs, CsOH, CsI and its dimer Cs₂I₂, with one up to three water molecules, are calculated to assess their possible existence in severe accident occurring to a pressurized water reactor. The calculations were performed using the coupled cluster theory including single, double and non-iterative triple substitutions (CCSD(T)) in conjunction with the basis sets (ANO-RCC) developed for scalar relativistic calculations. The second-order spin-free Douglas-Kroll-Hess Hamiltonian was used to account for the scalar relativistic effects. Thermodynamic properties obtained by these correlated ab initio calculations (entropies and thermal capacities at constant pressure as a function of temperature) are used in nuclear accident simulations using ASTEC/SOPHAEROS software. Interaction energies, standard enthalpies and Gibbs free energies of successive water molecules addition determine the ordering of the complexes. CsOH forms the most hydrated stable complexes followed by CsI, Cs₂I₂, and Cs. CsOH still exists in steam atmosphere even at quite high temperature, up to around 1100 K.

  16. Hydrothermal preparation of zeolite Li-A and ion exchange properties of Cs and Sr in salt waste

    International Nuclear Information System (INIS)

    Lee, S. H.; Kim, J. G.; Lee, J. H.; Kim, J. H.

    2005-01-01

    An advanced spent fuel management process that were based on Li reduction of the oxide spent fuel to a metallic form will generate a LiCl waste. Zeolite A has been reported as a promising immobilization medium for waste salt with CsCl and SrCl 2 . However, Sodium is accumulated as an ionic form (Na + -ion) in molten salt during ion exchange step between Na + -ion in zeolite A and Li + -ion in the molten salt. Therefore, zeolite Na-A need to be replaced by the Li-type zeolite for recycling the salt waste by removing the Cs and Sr ions. In this study, the hydrothermal preparation of zeolite Li-A was performed in 350ml pressure vessel by P. Norby method. The preparation characteristics of zeolite Li-A was investigated. And the ion exchange properties of Cs and Sr in molten LiCl salt were investigated under the condition of 923K using zeolite 4A and prepared zeolite Li-A

  17. Concentration and immobilization of 137Cs from liquid radioactive waste using sorbents based on hydrated titanium and zirconium oxides

    Science.gov (United States)

    Voronina, A. V.; Noskova, A. Y.; Gritskevich, E. Y.; Mashkovtsev, M. A.; Semenishchev, V. S.

    2017-09-01

    The possibility of use of sorbents based on hydrated titanium and zirconium oxides (T-3A, T-35, NPF-HTD) for concentration and immobilization of 137Cs from liquid radioactive waste of various chemical composition (fresh water, seawater, solutions containing NaNO3, ammonium acetate, EDTA) was evaluated. It was shown that the NPF-HTD and T-35 sorbents separate 137Cs from fresh water and seawater with distribution coefficients as high as 6.2.104 and 6.1.104, 4.0.105 and 1.6.105 L kg-1 respectively; in 1 M ammonium acetate these values were 2.0.103 and 1.0.103 L kg-1. The NPF-HTD sorbent showed the highest selectivity for cesium in NaNO3 solution: cesium distribution coefficients in 1M NaNO3 was 1.4.106 L kg-1. All studied sorbents are suitable for deactivation of solutions containing EDTA. Cesium distribution coefficients were around 102-103 L kg-1 depending on EDTA concentration. Chemical stability of the sorbents was also studied. It was shown that 137Cs leaching rate from all sorbents meet the requirements for matrix materials.

  18. CS-Studio Scan System Parallelization

    Energy Technology Data Exchange (ETDEWEB)

    Kasemir, Kay [ORNL; Pearson, Matthew R [ORNL

    2015-01-01

    For several years, the Control System Studio (CS-Studio) Scan System has successfully automated the operation of beam lines at the Oak Ridge National Laboratory (ORNL) High Flux Isotope Reactor (HFIR) and Spallation Neutron Source (SNS). As it is applied to additional beam lines, we need to support simultaneous adjustments of temperatures or motor positions. While this can be implemented via virtual motors or similar logic inside the Experimental Physics and Industrial Control System (EPICS) Input/Output Controllers (IOCs), doing so requires a priori knowledge of experimenters requirements. By adding support for the parallel control of multiple process variables (PVs) to the Scan System, we can better support ad hoc automation of experiments that benefit from such simultaneous PV adjustments.

  19. Correlations between potassium, rubidium and cesium (133Cs and 137Cs) in sporocarps of Suillus variegatus in a Swedish boreal forest

    International Nuclear Information System (INIS)

    Vinichuk, M.; Rosen, K.; Johanson, K.J.; Dahlberg, A.

    2011-01-01

    An analysis of sporocarps of ectomycorrhizal fungi Suillus variegatus assessed whether cesium ( 133 Cs and 137 Cs) uptake was correlated with potassium (K) or rubidium (Rb) uptake. The question was whether intraspecific correlations of Rb, K and 133 Cs mass concentrations with 137 Cs activity concentrations in sporocarps were higher within, rather than among, different fungal species, and if genotypic origin of sporocarps within a population affected uptake and correlation. Sporocarps (n = 51) from a Swedish forest population affected by the fallout after the Chernobyl accident were studied. The concentrations were 31.9 ± 6.79 g kg -1 for K (mean ± SD, dwt), 0.40 ± 0.09 g kg -1 for Rb, 8.7 ± 4.36 mg kg -1 for 133 Cs and 63.7 ± 24.2 kBq kg -1 for 137 Cs. The mass concentrations of 133 Cs correlated with 137 Cs activity concentrations (r = 0.61). There was correlation between both 133 Cs concentrations (r = 0.75) and 137 Cs activity concentrations (r = 0.44) and Rb, but the 137 Cs/ 133 Cs isotopic ratio negatively correlated with Rb concentration. Concentrations of K and Rb were weakly correlated (r = 0.51). The 133 Cs mass concentrations, 137 Cs activity concentrations and 137 Cs/ 133 Cs isotopic ratios did not correlate with K concentrations. No differences between, within or, among genotypes in S. variegatus were found. This suggested the relationships between K, Rb, 133 Cs and 137 Cs in sporocarps of S. variegatus is similar to other fungal species. - Highlights: → We studied uptake of Cs ( 133 Cs and 137 Cs), K and Rb by Suillus variegates sporocarps. → Genotypic origin of fungus did not affect uptake of studied elements (isotopes). → Genotypic origin did not affect correlation between Cs ( 133 Cs and 137 Cs), K and Rb.

  20. Determination of /sup 131/I, /sup 134/Cs, /sup 137/Cs in grass and cheese after Chernobyl accident in Austria

    Energy Technology Data Exchange (ETDEWEB)

    Teherani, D K

    1987-09-14

    Various samples from Styria (grass) and Salzburg (cheese) were analyzed for /sup 131/I, /sup 134/Cs and /sup 137/Cs concentration during April - July 1986 by ..gamma..-ray spectroscopy. The concentrations are reported in nCi kg/sup -1/ wet weight. The values found for /sup 131/I were 0.2-17.2 (grass), 0.1-0.5 (cheese), for /sup 134/Cs 1.1-6.2 (grass), 0.2-1.3 (cheese), for /sup 137/Cs 1.6-15.7 (grass), 0.3-2.2 (cheese). While radioactivity of /sup 131/I, /sup 134/Cs and /sup 137/Cs in cheese samples increased from May to June, it decreased in grass samples from May to July. (author) 5 refs

  1. Uptake and accumulation of 137Cs by upland grassland soil fungi: a potential pool of Cs immobilization

    International Nuclear Information System (INIS)

    Dighton, J.; Clint, G.M.; Poskitt, J.

    1991-01-01

    Reports of high concentrations of fallout radiocaesium in basidiomycete fruit bodies after the Chernobyl nuclear reactor accident and speculation that fungi could be long-term 137 Cs accumulators led us to ask if fungi could be long-term 137 Cs accumulators. We used six common upland grassland species to try to estimate their importance in the immobilization of 137 Cs. Uptake of Cs by these species ranged from 44 to 235 nmol Cs g − 1d.w. h − 1. Efflux studies indicate that more than 40% of the Cs taken up is bound within the hyphae. We estimate that the fungal component of the soil could immobilize the total radiocaesium fallout received in upland grasslands following the Chernobyl accident

  2. Coefficients of distribution and accumulation of K, Rb, Cs and 137Cs in the intensive poultry breeding cycle

    International Nuclear Information System (INIS)

    Djuric, G.; Ajdacic, N.; Institut za Nuklearne Nauke Boris Kidric, Belgrade

    1984-01-01

    The concentration of K,Rb,Cs and the activity level of Cs-137 in samples from the intensive poultry breeding cycle (feed, meat, eggs), under the condition of chronic alimentary contamination is presented. Concentrations of Cs and Rb were determined by non-destructive neutron activation analysis, concentration of K by atomic absorption flame photometry and activity of Cs-137 by gamma spectrometric analysis. On the basis of these results, coefficients of distribution and accumulation were calculated. The distribution coefficients of the analysed stable isotopes in meat have values close to 1, whereas for various parts of egg these coefficients vary between 0.5 and 1.5. Significant differences in Cs-137 distribution in various parts of egg were established. The values of accumulation coefficients indicate that all analysed elements selectively accumulate in the meat of young birds (broilers), and Cs-137 accumulates in the egg white as well. (orig.)

  3. Phase Transitions in CsSnCl3 and CsPbBr3 An NMR and NQR Study

    Science.gov (United States)

    Sharma, Surendra; Weiden, Norbert; Weiss, Alarich

    1991-04-01

    The phase transitions in CsSnCl3 and CsPbBr3 have been studied by X-ray powder diffraction, by 81Br-NQR and by 'H-, 119Sn-, and 113Cs-NMR. At room temperature in air CsSnCl3 forms a hydrate which can be dehydrated to the monoclinic phase II of CsSnCl3. The high temperature phase I has the Perovskite structure, as the X-ray and NMR experiments show. The three phases of CsPbBr3, known from literature, have been corroborated. The results are discussed in the framework of the group ABX3, A = alkalimetal ion, B = IV main group ion, and X = Halogen ion

  4. Biosorption of Am-241 and Cs-137 by radioactive liquid waste by coffee husk

    Energy Technology Data Exchange (ETDEWEB)

    Ferreira, Rafael Vicente de Padua; Sakata, Solange Kazumi; Bellini, Maria Helena; Marumo, Julio Takehiro, E-mail: jtmarumo@ipen.b [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2011-07-01

    Radioactive Waste Management Laboratory of Nuclear and Energy Research Institute, IPEN-CNEN/SP, has stored many types of radioactive liquid wastes, including liquid scintillators, mixed wastes from chemical analysis and spent decontamination solutions. These wastes need special attention, because the available treatment processes are often expensive and difficult to manage. Biosorption using biomass of vegetable using agricultural waste has become a very attractive technique because it involves the removal of heavy metals ions by low cost biossorbents. The aim of this study is to evaluate the potential of the coffee husk to remove Am-241 and Cs-137 from radioactive liquid waste. The coffee husk was tested in two forms, treated and untreated. The chemical treatment of the coffee husk was performed with HNO{sub 3} and NaOH diluted solutions. The results showed that the coffee husk did not showed significant differences in behavior and capacity for biosorption for Am-241 and Cs-137 over time. Coffee husk showed low biosorption capacity for Cs-137, removing only 7.2 {+-} 1.0% in 4 hours of contact time. For Am-241, the maximum biosorption was 57,5 {+-} 0.6% in 1 hours. These results suggest that coffee husk in untreated form can be used in the treatment of radioactive waste liquid containing Am-241. (author)

  5. Removal of 137-Cs from Dissolved Hanford Tank Saltcake by Treatment with IE-911

    International Nuclear Information System (INIS)

    Rapko, Brian M.; Sinkov, Sergei I.; Levitskaia, Tatiana G.

    2003-01-01

    The U.S. Department of Energy's Richland Operations Office plans to accelerate the cleanup of the Hanford Site. Testing new technology for the accelerated cleanup will require dissolved saltcake from single-shell tanks. However, the 137Cs will need to be removed from the saltcake to alleviate radiation hazards. A saltcake composite constructed from archived samples from Hanford Site single-shell tanks 241-S-101, 241-S-109, 241-S-110, 241-S-111, 241-U-106, and 241-U-109 was dissolved in water, adjusted to 5 M Na, and transferred from the 222-S Laboratory to the Radiochemical Processing Laboratory (RPL). At the RPL, the approximately 5.5 liters of solution was passed through a 0.2-micron polyethersulfone filter, collected, and homogenized. The filtered solution then was passed through an ion exchange column containing approximately 150 mL IONSIV(reg s ign) IE-911, an engineered form of crystalline silicotitanate available from UOP, at approximately 200 mL/hour in a continuous operation until all of the feed solution had been run through the column. An analysis of the 137Cs concentrations in the initial feed solution and combined column effluent indicates that > 99.999 percent of the Cs in the feed solution was removed by this operation

  6. The removal of 134Cs from radioactive process waste water by coprecipitate flotation

    International Nuclear Information System (INIS)

    Aziz, M.; Shakir, K.; Benyamin, K.

    1986-01-01

    The coprecipitate flotation of 134 Cs from radioactive process waste water using copper ferrocyanide as a coprecipitating agent and sodium lauryl sulphate, cetyl trimethyl ammonium bromide or gelatin as collector was extensively investigated to establish the best conditions for caesium removal with each of the collectors under test. The investigated parameters include the collector dosage, the Cu 2+ /Fe(CN) 6 4- ratio, the caesium, potassium, sodium and calcium ion concentrations, the ageing time period of the Cu 2+ - Fe(CN) 6 4- - 134 Cs - water system and the bubbling time duration. The results indicate that copper ferrocyanide has a high affinity for caesium and can preferentially co-precipitate it in presence of relatively high amounts of other alkali or alkaline earth cations. For the alkali metals the affinity increases in the order Na < K < Cs. Under the optimal conditions removals higher than 99% could be achieved with any of the tested collectors. The results are discussed in terms of the ion exchange properties of copper ferrocyanide and collector behaviour. Advantages of the coflotation technique over other methods are enumerated. (Auth.)

  7. Biosorption of Am-241 and Cs-137 by radioactive liquid waste by coffee husk

    International Nuclear Information System (INIS)

    Ferreira, Rafael Vicente de Padua; Sakata, Solange Kazumi; Bellini, Maria Helena; Marumo, Julio Takehiro

    2011-01-01

    Radioactive Waste Management Laboratory of Nuclear and Energy Research Institute, IPEN-CNEN/SP, has stored many types of radioactive liquid wastes, including liquid scintillators, mixed wastes from chemical analysis and spent decontamination solutions. These wastes need special attention, because the available treatment processes are often expensive and difficult to manage. Biosorption using biomass of vegetable using agricultural waste has become a very attractive technique because it involves the removal of heavy metals ions by low cost biossorbents. The aim of this study is to evaluate the potential of the coffee husk to remove Am-241 and Cs-137 from radioactive liquid waste. The coffee husk was tested in two forms, treated and untreated. The chemical treatment of the coffee husk was performed with HNO 3 and NaOH diluted solutions. The results showed that the coffee husk did not showed significant differences in behavior and capacity for biosorption for Am-241 and Cs-137 over time. Coffee husk showed low biosorption capacity for Cs-137, removing only 7.2 ± 1.0% in 4 hours of contact time. For Am-241, the maximum biosorption was 57,5 ± 0.6% in 1 hours. These results suggest that coffee husk in untreated form can be used in the treatment of radioactive waste liquid containing Am-241. (author)

  8. Study of contamination with 137Cs

    International Nuclear Information System (INIS)

    Silva, A.G. da.

    1987-01-01

    The methodology and results of measurements accomplished (from October 30 to November 2,87) in a victim of an accident in Goiania (Brazil) are presented. Superficial and whole-body contamination using NaI detectors and Si-Au surface screens are studied. (M.A.C.) [pt

  9. Synthesis and crystallographic study of the compounds in the system Cs{sub 2}O - Al{sub 2}O{sub 3} - SiO{sub 2}; Synthese et etude cristallographique des composes du systeme Cs{sub 2}O - Al{sub 2}O{sub 3} - SiO{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

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

    1969-05-01

    A study has been made on the preparation, structure and thermal evolution of some definite compounds in the system: Cs{sub 2}O - Al{sub 2}O{sub 3} - SiO{sub 2}. Precise details are given about the structure of the following compounds: CsAlO{sub 2}, RbAlO{sub 2}, KAlO{sub 2} and NaAlO{sub 2}; CsAlO{sub 2}, 2 H{sub 2}O; Cs{sub 2}O, 11 Al{sub 2}O{sub 3}; Cs{sub 2}O, 2 SiO{sub 2}; Cs{sub 2}O, 4 SiO{sub 2} and Rb{sub 2}O, 4 SiO{sub 2}; CsAlSiO{sub 4}; CsAlSi{sub 2}O{sub 6}; Cs{sub 4}Ge{sub 11}O{sub 24} and Rb{sub 4}Ge{sub 11}O{sub 24}. The long term purpose of this work was to find a compound which would be insoluble, refractory and at the same time able to contain radioactive isotopes of cesium and thus suitable as radiation sources. The knowledge of the properties and structure of aluminates, silicates and aluminosilicates is a necessary stage before the elaboration of ceramic caesium sources. The compound which seems quite convenient for this use, Cs{sub 2}AlSi{sub 2}O{sub 6}, is closely related to the natural mineral 'pollucite', and offers interesting properties. (author) [French] Ce travail constitue une etude de la preparation, de la structure et de l'evolution thermique des composes definis du systeme: Cs{sub 2}O - Al{sub 2}O{sub 3} - SiO{sub 2} et de quelques homologues. Des precisions sont donnees sur la structure des composes suivants: CsAlO{sub 2}, RbAlO{sub 2}, KAlO{sub 2} et NaAlO{sub 2}; CsAlO{sub 2}, 2 H{sub 2}O; Cs{sub 2}O, 11 Al{sub 2}O{sub 3}; Cs{sub 2}O, 2 SiO{sub 2}; Cs{sub 2}O, 4 SiO{sub 2} et Rb{sub 2}O, 4 SiO{sub 2}; CsAlSiO{sub 4}; CsAlSi{sub 2}O{sub 6}; Cs{sub 4}Ge{sub 11}O{sub 24} et Rb{sub 4}Ge{sub 11}O{sub 24}. Le but a long terme de cette etude consistait a obtenir un compose a la fois refractaire et insoluble, susceptible de contenir un isotope radioactif du caesium, et d'etre utilise comme source de rayonnement. La connaissance des proprietes et de la structure des aluminates, silicates et aluminosilicates represente une etape necessaire

  10. Exploring Polaronic, Excitonic Structures and Luminescence in Cs4PbBr6/CsPbBr3.

    Science.gov (United States)

    Kang, Byungkyun; Biswas, Koushik

    2018-02-15

    Among the important family of halide perovskites, one particular case of all-inorganic, 0-D Cs 4 PbBr 6 and 3-D CsPbBr 3 -based nanostructures and thin films is witnessing intense activity due to ultrafast luminescence with high quantum yield. To understand their emissive behavior, we use hybrid density functional calculations to first compare the ground-state electronic structure of the two prospective compounds. The dispersive band edges of CsPbBr 3 do not support self-trapped carriers, which agrees with reports of weak exciton binding energy and high photocurrent. The larger gap 0-D material Cs 4 PbBr 6 , however, reveals polaronic and excitonic features. We show that those lattice-coupled carriers are likely responsible for observed ultraviolet emission around ∼375 nm, reported in bulk Cs 4 PbBr 6 and Cs 4 PbBr 6 /CsPbBr 3 composites. Ionization potential calculations and estimates of type-I band alignment support the notion of quantum confinement leading to fast, green emission from CsPbBr 3 nanostructures embedded in Cs 4 PbBr 6 .

  11. Transepithelial Na+ transport and the intracellular fluids: a computer study.

    Science.gov (United States)

    Civan, M M; Bookman, R J

    1982-01-01

    Computer simulations of tight epithelia under three experimental conditions have been carried out, using the rheogenic nonlinear model of Lew, Ferreira and Moura (Proc. Roy. Soc. London. B 206:53-83, 1979) based largely on the formulation of Koefoed-Johnsen and Ussing (Acta Physiol. Scand. 42: 298-308. 1958). First, analysis of the transition between the short-circuited and open-circuited states has indicated that (i) apical Cl- permeability is a critical parameter requiring experimental definition in order to analyze cell volume regulation, and (ii) contrary to certain experimental reports, intracellular Na+ concentration (ccNa) is expected to be a strong function of transepithelial clamping voltage. Second, analysis of the effects of lowering serosal K+ concentration (csK) indicates that the basic model cannot simulate several well-documented observations; these defects can be overcome, at least qualitatively, by modifying the model to take account of the negative feedback interaction likely to exist between the apical Na+ permeability and ccNa. Third, analysis of the strongly supports the concept that osmotically induced permeability changes in the apical intercellular junctions play a physiological role in conserving the body's stores of NaCl. The analyses also demonstrate that the importance of Na+ entry across the basolateral membrane is strongly dependent upon transepithelial potential, cmNa and csK; under certain conditions, net Na+ entry could be appreciably greater across the basolateral than across the apical membrane.

  12. Decontamination of Soils Contaminated with Co and Cs by Using an Acid Leaching Process

    International Nuclear Information System (INIS)

    Jung-Joon, Lee; Gye-Nam, Kim; Jei-Kwon, Moon; Kune-Woo, Lee

    2009-01-01

    Acid leaching process has been adapted for the remediation of soils contaminated with heavy metals and radionuclides. This method has been reported to be simple, and economically promising. Moreover it can be applicable for on-site and off-site remediations as well. Investigations were conducted on an acid leaching process using surrogate contaminated soils. Size sieving, agglomeration and column leaching were carried out with soils artificially contaminated with Co and Cs, respectively. Size distribution was analyzed for a determination of the particle size required to be agglomerated. Because of the low water permeability of the soils due to their fine particles, they were sieved by using a sieve with a 0.075 mm size (No. 200 mesh) for an agglomeration. The soils with a size smaller than 0.075 mm were agglomerated by using 2 % sodium silicate (Na 2 SiO 3 ), while the soils with a size larger than 0.075 mm were used directly for the column leaching test. From the preliminary test (the batch scale leaching test), 0.1 M of HCl was determined as the effective leaching agent for Co and Cs. Finally, the soils mixed with the coarse soil and the agglomerated soil were decontaminated with 0.1 M HCl within 11.3 days and the removal efficiencies of Co and Cs were 94.0 % and 82.8 %, respectively. In conclusion, an acid leaching process could be applied for a remediation of soils contaminated with radionuclides such as Co and Cs. (authors)

  13. Distribution and behavior of {sup 137}Cs in undisturbed soil

    Energy Technology Data Exchange (ETDEWEB)

    Satta, Naoya [Kyoto Univ., Kumatori, Osaka (Japan). Research Reactor Inst.

    1996-04-01

    The depth distribution of {sup 137}Cs in soils which has not been artificially disturbed for 100 years was compared to fallout history. The model of {sup 137}Cs distribution rate was established to estimate fallout history from soil samples. (J.P.N.)

  14. Relative volatility of dilute solutions of Rb-Cs system

    International Nuclear Information System (INIS)

    Gromov, P.B.; Izotov, V.P.; Nisel'son, L.A.

    1984-01-01

    Relative volatility of diluted solutions Rb-Cs in the temperature range 650-820 K and pressures 13-200 gPa has been studied. The system Rb-Cs in the range of diluted solutions obeys the Henry law. It is shown, that liquid-vapour equilibrium in diluted solutions of cesium in rubidium is characterized by negative deviation from perfection

  15. Direct and indirect contamination of tree crops with Cs-134

    International Nuclear Information System (INIS)

    Skarlou, V.; Nobeli, C.; Anoussis, J.; Arapis, G.; Haidouti, C.

    1996-01-01

    A long term glasshouse pot experiment was established in 1994 to study the transfer factors of Cs-134 from soil to olive and orange trees for which no relevant data are available. A calcareous-heavy textured and an acid-light textured soil were used in this experiment. Results from two year's experimentation are considered in this study. The ability of the studied plant species for Cs-134 root uptake seems to be significantly influenced by soil type. The contamination of both tree species grown on calcareous and heavy soil was very low and did not change much with the time. On the contrary, trees grown on acid and light soil showed much higher Cs-134 concentration (up to 34 times for orange and 23 for olive trees) which significantly increased with the time. Both olive and orange trees showed a similar behaviour in the studied soils. Effort was also made to study the long term consequences of the direct contamination in a field experiment where an olive tree was contaminated by dry deposition with Cs-134. Six months after contamination 5 % of the Cs-134 deposited on the leaves was measured in the first olive production. However, very small quantities (= 0.5 %) of the olive Cs-134 was detected in the unprocessed olive oil. The following year 15 % of the Cs-134 remained in the leaves while extremely low quantities of Cs-134 were detected in either olives or olive oil. (author)

  16. Antibodies derived from an enterotoxigenic Escherichia coli (ETEC) adhesin tip MEFA (multiepitope fusion antigen) against adherence of nine ETEC adhesins: CFA/I, CS1, CS2, CS3, CS4, CS5, CS6, CS21 and EtpA.

    Science.gov (United States)

    Nandre, Rahul M; Ruan, Xiaosai; Duan, Qiangde; Sack, David A; Zhang, Weiping

    2016-06-30

    Diarrhea continues to be a leading cause of death in children younger than 5 years in developing countries. Enterotoxigenic Escherichia coli (ETEC) is a leading bacterial cause of children's diarrhea and travelers' diarrhea. ETEC bacteria initiate diarrheal disease by attaching to host receptors at epithelial cells and colonizing in small intestine. Therefore, preventing ETEC attachment has been considered the first line of defense against ETEC diarrhea. However, developing vaccines effectively against ETEC bacterial attachment encounters challenge because ETEC strains produce over 23 immunologically heterogeneous adhesins. In this study, we applied MEFA (multiepitope fusion antigen) approach to integrate epitopes from adhesin tips or adhesive subunits of CFA/I, CS1, CS2, CS3, CS4, CS5, CS6, CS21 and EtpA adhesins and to construct an adhesin tip MEFA peptide. We then examined immunogenicity of this tip MEFA in mouse immunization, and assessed potential application of this tip MEFA for ETEC vaccine development. Data showed that mice intraperitoneally immunized with this adhesin tip MEFA developed IgG antibody responses to all nine ETEC adhesins. Moreover, ETEC and E. coli bacteria expressing these nine adhesins, after incubation with serum of the immunized mice, exhibited significant reduction in attachment to Caco-2 cells. These results indicated that anti-adhesin antibodies induced by this adhesin tip MEFA blocked adherence of the most important ETEC adhesins, suggesting this multivalent tip MEFA may be useful for developing a broadly protective anti-adhesin vaccine against ETEC diarrhea. Copyright © 2016 Elsevier Ltd. All rights reserved.

  17. Is 137Cs Dating Becoming Obsolete in North America?

    Science.gov (United States)

    Drexler, J. Z.; Fuller, C.; Salas, A.

    2016-12-01

    Dating of wetland sediments and peat is routinely carried out using 137Cs and 210Pb analysis. Unlike 210Pb, 137Cs is an anthropogenic radionuclide with a history of fallout from nuclear weapons testing. 137Cs is used as a single time marker; its peak is coincident with the height of atmospheric nuclear testing in 1963/4. During its use in the 1970s-90s, 137Cs peaks were usually highly distinct in wetland sediments (e.g., see 137Cs peaks from Louisiana marshes in Feijtel et al., 1988). This enabled its use as a check for dates assigned to a profile by 210Pb and other methods. However, recently, the efficacy of 137Cs dating in North America has deteriorated. In this presentation, we will provide specific examples of 137Cs as well as 210Pb dating in wetland sediments/peats we collected between 2005 and 2015 in Maine, California, Virginia, North Carolina, South Carolina, and Washington. Two main reasons exist for this decline. First, 137Cs activities in our recent cores are 30-40 % of the original activities in 1963/4 due to decay of the original 137Cs in situ (half-life = 30.17 years) and no major new sources. This manifests in lower signal to noise ratio, with some peaks barely recognizable above the noise. Second, 137Cs peaks are much less distinct due to 137Cs migration through time independent of substrate (or sediment) particles. Migration of peaks has resulted in estimated accretion rates being systematically lower or higher than those derived from 210Pb dating. These issues with 137Cs dating have important implications because 137Cs is used with 210Pb dating or even alone to determine rates of recent wetland carbon accumulation. Such rates are required to enter wetland restoration projects into carbon markets and to document IPCC mandated reductions in carbon pollution. Our analysis shows that, although dating by 137Cs alone has always been highly tenuous, now it is especially contraindicated and should be disallowed for the purposes of carbon accounting.

  18. Determination of {sup 135}Cs by accelerator mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    MacDonald, C.M.; Charles, C.R.J. [Andre. E. Lalonde AMS Laboratory, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5 (Canada); Department of Earth Sciences, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5 (Canada); Zhao, X.-L.; Kieser, W.E. [Andre. E. Lalonde AMS Laboratory, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5 (Canada); Department of Physics, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5 (Canada); Cornett, R.J. [Andre. E. Lalonde AMS Laboratory, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5 (Canada); Department of Earth Sciences, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5 (Canada); Litherland, A.E. [IsoTrace Laboratory, University of Toronto, 60 St. George St., Toronto, ON M5S 1A7 (Canada)

    2015-10-15

    The ratio of anthropogenic {sup 135}Cs and {sup 137}Cs isotopes is characteristic of a uranium fission source. This research evaluates the technique of isotope dilution (yield tracing) for the purpose of quantifying {sup 135}Cs by accelerator mass spectrometry with on-line isobar separation. Interferences from Ba, Zn{sub 2}, and isotopes of equal mass to charge ratios were successfully suppressed. However, some sample crosstalk from source contamination remains. The transmission and di-fluoride ionization efficiencies of Cs isotopes were found to be 8 × 10{sup −3} and 1.7 × 10{sup −7} respectively. This quantification of {sup 135}Cs using yield tracing by accelerator mass spectrometry shows promise for future environmental sample analysis once the issues of sample crosstalk and low efficiency can be resolved.

  19. Recovery of Cs from high level radioactive waste

    International Nuclear Information System (INIS)

    Kumar, Amar; Kaushik, C.P.; Raj, K.; Varshney, Lalit

    2008-01-01

    Separation of Cs + from HLW restricts the personal radiation exposure during the vitrification and prevents thermal deformation of conditioned waste matrix during storage because of the high calorific power of 134 Cs (13.18 W/g) and 137 Cs (0.417 W/g) which would markedly reduce the storage cost. Separation will also reduce its volatility during vitrification and extent of migration from the vitrified mass in repository. In addition 137 Cs has enormous applications as radiation sources in food preservation, sterilization of medical products, brachy therapy, blood irradiation, hygienization of sewage sludge etc. The use of 137 Cs (T 1/2 = 30 years) in place of 60 Co (T 1/2 = 5.2 years) will also reduce the shielding requirement and frequency of source replenishment which will ease the handling/transportation of radioactive source

  20. Transformation of Sintered CsPbBr3 Nanocrystals to Cubic CsPbI3 and Gradient CsPbBrxI3-x through Halide Exchange.

    Science.gov (United States)

    Hoffman, Jacob B; Schleper, A Lennart; Kamat, Prashant V

    2016-07-13

    All-inorganic cesium lead halide (CsPbX3, X = Br(-), I(-)) perovskites could potentially provide comparable photovoltaic performance with enhanced stability compared to organic-inorganic lead halide species. However, small-bandgap cubic CsPbI3 has been difficult to study due to challenges forming CsPbI3 in the cubic phase. Here, a low-temperature procedure to form cubic CsPbI3 has been developed through a halide exchange reaction using films of sintered CsPbBr3 nanocrystals. The reaction was found to be strongly dependent upon temperature, featuring an Arrhenius relationship. Additionally, film thickness played a significant role in determining internal film structure at intermediate reaction times. Thin films (50 nm) showed only a small distribution of CsPbBrxI3-x species, while thicker films (350 nm) exhibited much broader distributions. Furthermore, internal film structure was ordered, featuring a compositional gradient within film. Transient absorption spectroscopy showed the influence of halide exchange on the excited state of the material. In thicker films, charge carriers were rapidly transferred to iodide-rich regions near the film surface within the first several picoseconds after excitation. This ultrafast vectorial charge-transfer process illustrates the potential of utilizing compositional gradients to direct charge flow in perovskite-based photovoltaics.

  1. Na/K Pump and Beyond: Na/K-ATPase as a Modulator of Apoptosis and Autophagy.

    Science.gov (United States)

    Felippe Gonçalves-de-Albuquerque, Cassiano; Ribeiro Silva, Adriana; Ignácio da Silva, Camila; Caire Castro-Faria-Neto, Hugo; Burth, Patrícia

    2017-04-21

    Lung cancer is a leading cause of global cancer deaths. Na/K-ATPase has been studied as a target for cancer treatment. Cardiotonic steroids (CS) trigger intracellular signalling upon binding to Na/K-ATPase. Normal lung and tumour cells frequently express different pump isoforms. Thus, Na/K-ATPase is a powerful target for lung cancer treatment. Drugs targeting Na/K-ATPase may induce apoptosis and autophagy in transformed cells. We argue that Na/K-ATPase has a role as a potential target in chemotherapy in lung cancer treatment. We discuss the effects of Na/K-ATPase ligands and molecular pathways inducing deleterious effects on lung cancer cells, especially those leading to apoptosis and autophagy.

  2. Na/K Pump and Beyond: Na/K-ATPase as a Modulator of Apoptosis and Autophagy

    Directory of Open Access Journals (Sweden)

    Cassiano Felippe Gonçalves-de-Albuquerque

    2017-04-01

    Full Text Available Lung cancer is a leading cause of global cancer deaths. Na/K-ATPase has been studied as a target for cancer treatment. Cardiotonic steroids (CS trigger intracellular signalling upon binding to Na/K-ATPase. Normal lung and tumour cells frequently express different pump isoforms. Thus, Na/K-ATPase is a powerful target for lung cancer treatment. Drugs targeting Na/K-ATPase may induce apoptosis and autophagy in transformed cells. We argue that Na/K-ATPase has a role as a potential target in chemotherapy in lung cancer treatment. We discuss the effects of Na/K-ATPase ligands and molecular pathways inducing deleterious effects on lung cancer cells, especially those leading to apoptosis and autophagy.

  3. Soil 137Cs background values in monsoon region of china

    International Nuclear Information System (INIS)

    Zhang Mingli; Yang Hao; Wang Xiaolei; Wang Yihong; Xu Congan; Yang Jiudong; Rong Jing

    2009-01-01

    Land degradation,, which is resulted from the soil erosion, is one of the major environmental problems. It severely affects the food supplies, environmental safety and the sustainable development in China. Some areas in the monsoon region are suffering from the acute soil erosion. To find out the degree of soil erosion, the proven technique of 137 Cs tracer is definitely one of the best methods, and the key is to ascertain the accuracy of soil 137 Cs background value. The distributions of 137 Cs were explored in soil profiles by detecting the 137 Cs of soil cores from the Yimeng mountain area in Shandong Province, hills in the southern area of Jiangsu Province and Dianchi catchment in Yunnan Province, respectively. We found that the depth of 137 Cs distribution is not the same in the soils of various areas. But the 137 Cs activity shows an exponential distribution in the uncultivated soil and demonstrates a strong correlation with the soil depth, while the 137 Cs activity proves uniform in the soil plowing layer of the cultivated land. The study shows the 137 Cs background values of three areas: 1737.1 Bq/m 2 in Yimeng mountain area, 1847.6 Bq/m 2 in southern area of hills in Jiangsu, 918.0 Bq/m 2 in Dianchi catchment. The certainty of 137 Cs background value can technically support the use of 137 Cs technique to study the spatial pattern of soil erosion, deposition and the land degradation, which provides the support for the sustainable utilization of soil resource, the assessment of economical benefit and loss and the evaluation of water and soil conservation measures. (authors)

  4. Rapid determination of {sup 135}Cs and precise {sup 135}Cs/{sup 137}Cs atomic ratio in environmental samples by single-column chromatography coupled to triple-quadrupole inductively coupled plasma-mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Guosheng [Department of Radiation Chemistry, Institute of Radiation Emergency Medicine, Hirosaki University, 66-1 Hon-cho, Hirosaki, Aomori 036-8564 (Japan); Division of Nuclear Technology and Applications, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049 (China); Beijing Engineering Research Center of Radiographic Techniques and Equipment, Beijing 100049 (China); Tazoe, Hirofumi [Department of Radiation Chemistry, Institute of Radiation Emergency Medicine, Hirosaki University, 66-1 Hon-cho, Hirosaki, Aomori 036-8564 (Japan); Yamada, Masatoshi, E-mail: myamada@hirosaki-u.ac.jp [Department of Radiation Chemistry, Institute of Radiation Emergency Medicine, Hirosaki University, 66-1 Hon-cho, Hirosaki, Aomori 036-8564 (Japan)

    2016-02-18

    For source identification, measurement of {sup 135}Cs/{sup 137}Cs atomic ratio not only provides information apart from the detection of {sup 134}Cs and {sup 137}Cs, but it can also overcome the application limit that measurement of the {sup 134}Cs/{sup 137}Cs ratio has due to the short half-life of {sup 134}Cs (2.06 y). With the recent advancement of ICP-MS, it is necessary to improve the corresponding separation method for rapid and precise {sup 135}Cs/{sup 137}Cs atomic ratio analysis. A novel separation and purification technique was developed for the new generation of triple-quadrupole inductively coupled plasma-mass spectrometry (ICP-MS/MS). The simple chemical separation, incorporating ammonium molybdophosphate selective adsorption of Cs and subsequent single cation-exchange chromatography, removes the majority of isobaric and polyatomic interference elements. Subsequently, the ICP-MS/MS removes residual interference elements and eliminates the peak tailing effect of stable {sup 133}Cs, at m/z 134, 135, and 137. The developed analytical method was successfully applied to measure {sup 135}Cs/{sup 137}Cs atomic ratios and {sup 135}Cs activities in environmental samples (soil and sediment) for radiocesium source identification. - Highlights: • A simple {sup 135}Cs/{sup 137}Cs analytical method was developed. • The separation procedure was based on AMP adsorption and one column chromatography. • {sup 135}Cs/{sup 137}Cs was measured by ICP-MS/MS. • Decontamination factors for Ba, Mo, Sb, and Sn were improved. • {sup 135}Cs/{sup 137}Cs atomic ratios of 0.341–0.351 were found in Japanese soil samples.

  5. Bacterial CS2 Hydrolases from Acidithiobacillus thiooxidans Strains Are Homologous to the Archaeal Catenane CS2 Hydrolase

    NARCIS (Netherlands)

    Smeulders, M.J.; Pol, A. van der; Venselaar, H.; Barends, T.R.; Hermans, J.; Jetten, M.S.M.; Camp, H.J.M. op den

    2013-01-01

    Carbon disulfide (CS2) and carbonyl sulfide (COS) are important in the global sulfur cycle, and CS2 is used as a solvent in the viscose industry. These compounds can be converted by sulfur-oxidizing bacteria, such as Acidithiobacillus thiooxidans species, to carbon dioxide (CO2) and hydrogen sulfide

  6. Radioecological studies of 137Cs in limnological ecosystems. Biochemical states of 137Cs accumulated in killifish (Medaka, Oryzias latipes) meat

    International Nuclear Information System (INIS)

    Miyake, Sadaaki; Motegi, Misako; Oosawa, Takashi; Nakazawa, Kiyoaki; Izumo, Yoshiro; Nakamura, Fumio.

    1997-01-01

    Biochemical states of 137 Cs accumulated in killifish's (Medaka, Oryzias latipes) meat were investigated in order to elucidate the accumulation mechanism of the radionuclide in goldfish, Carassius auratus auratus, examined in our preceding report. Most of 137 Cs radioactivity in the killifish's raw meat accumulated this radionuclide in the radioactive freshwater, were found in the non-protein nitrogenous compound (NPNC) fraction (>92%), also in the killifish's control raw meat mixed with 137 Cs, the difference between both meat samples was not clear. As the results of gel filtration profiles on Sephadex G-25 for the NPNC fraction of these meats, each only one radioactive peak was shown, also similar to 137 CsCl solution. Moreover, these peaks appeared at the same position. On the other hand, the peak positions absorbed at OD 280nm in the samples were different from those of each radioactive peak. It was so suggested that 137 Cs accumulated in the killifish's meat was shown not to be binding to protein's composition. Furthermore, as the results on thin-layer chromatography, ion-exchange resin chromatography and reaction with 137 Cs in samples and ammonium phosphomolybdate, 137 Cs in the NPNC fraction of the killifish's meat was not almost different from those of each control and 137 CsCl solution. (author)

  7. Cs/CsPbX3 (X = Br, Cl) epitaxial heteronanocrystals with magic-angle stable/metastable grain boundary

    Science.gov (United States)

    Zhang, Yumeng; Fan, Baolu; Wu, Wenhui; Fan, Jiyang

    2017-05-01

    Metal-semiconductor heteronanostructures are crucial building blocks of nanoscale electronic and optoelectronic devices. However, the lattice misfit remains a challenge in constructing heteronanostructures. Perovskite nanocrystals are superior candidates for constructing nanodevices owing to excellent optical, ferroelectric, and superconducting properties. We report the epitaxial growth of lattice-matched Cs/CsPbBr3 metal-semiconductor heteronanocrystals in a liquid medium. The well-crystallized ultrathin Cs layers grow epitaxially on the surfaces of colloidal CsPbBr3 nanocrystals, forming heteronanocrystals with interface diameters of several nanometers. Most of them are pseudomorphic with coherent interfaces free from dislocations, and the others exhibit discrete high-angle grain boundaries. The model based on the calculation of the elastic potential energy of the epilayer and analysis of the near-coincidence sites explains well the experimental result. The analysis shows that the excellent lattice match between the metal and the semiconductor ensures the ideal epitaxial-growth of both Cs/CsPbBr3 and Cs/CsPbCl3 heteronanocrystals. Such metal/semiconductor heteronanocrystals pave the way for developing perovskite-based nanodevices.

  8. A second generation Cs BEC experiment

    International Nuclear Information System (INIS)

    Gustavsson, M.; Unterwaditzer, P.; Naegerl, H.-C.

    2004-01-01

    We present a new experiment currently under construction in Innsbruck. A Cs BEC will be produced in a glass cell apparatus, allowing maximum optical access and rapid switching of magnetic fields. A high loading rate and a large-volume optical dipole trap at near infrared wavelengths together with optimized 3D Raman sideband cooling should allow for large condensates with more than 10 6 atoms. We plan to load the BEC into a 3D optical lattice. With precisely two or three atoms per site and s-wave interactions tunable through Feshbach resonances at low magnetic fields, it will be possible to study collisions and molecule formation in a very controlled environment. The formation of a molecular BEC made out of bosonic constituents might be stabilized with help of the lattice. A further possible application is the measurement of clock shifts. Another interesting possibility is to study the regime of zero scattering length. A BEC without perturbing mean-field shifts is ideally suited for atom interferometry and precision measurements. For example, it is possible to determine the fine structure constant alpha via measurement of the photon recoil. (author)

  9. Epiphytic fruticose lichens as biomonitors for retrospective evaluation of the 134Cs/137Cs ratio in Fukushima fallout

    International Nuclear Information System (INIS)

    Ramzaev, V.; Barkovsky, A.; Gromov, A.; Ivanov, S.; Kaduka, M.

    2014-01-01

    In 2011–2013, sampling of epiphytic fruticose lichens of the genera Usnea, Bryoria and Alectoria was carried out on Sakhalin and Kuril Islands (the Sakhalin region, Russia) to investigate contamination of these organisms with the Fukushima-derived 134 Cs and 137 Cs. Activities of the radionuclides were determined in all 56 samples of lichens taken for the analysis. After correction for radioactive decay (on 15 March 2011), the activity concentrations ranged from 2.1 Bq kg −1 (d.w.) to 52 Bq kg −1 for 134 Cs and from 2.3 Bq kg −1 to 52 Bq kg −1 for 137 Cs. Cesium-134 and 137 Cs activities for the whole set of lichens (n = 56) were strongly positively correlated; Spearman's rank correlation coefficient was calculated as 0.991 (P < 0.01). The activity concentrations of 134 Cs and 137 Cs in Usnea lichens from the Sakhalin and Kunashir islands declined with a factor of three in the period from 2011 to 2013. The average biological half-time for both cesium radionuclides in lichens of the genus Usnea is estimated as 1.3 y. The mean of 0.99 ± 0.10 and median of 0.99 were calculated for the decay corrected 134 Cs/ 137 Cs activities ratios in the lichens (n = 56). The radionuclides ratio in the lichens did not depend on location of sampling site, species and the time that had passed after the Fukushima accident. The regression analysis has shown the background pre-Fukushima level of 137 Cs of 0.4 ± 0.3 Bq kg −1 , whereas the ratio between the Fukushima-borne 134 Cs and 137 Cs in the lichens was estimated as 1.04. The 134 Cs/ 137 Cs activities ratio in lichens from the Sakhalin region is consistent with the ratios reported by others for the heavy contaminated areas on Honshu Island in Japan following the Fukushima accident. The activity concentrations of natural 7 Be in lichens from the Sakhalin region varied between 100 Bq kg −1 and 600 Bq kg −1 ; the activity concentrations did not exhibit temporal variations during a 2y-period of observations. The

  10. Photoresponse of CsPbBr3 and Cs4PbBr6 Perovskite Single Crystals.

    Science.gov (United States)

    Cha, Ji-Hyun; Han, Jae Hoon; Yin, Wenping; Park, Cheolwoo; Park, Yongmin; Ahn, Tae Kyu; Cho, Jeong Ho; Jung, Duk-Young

    2017-02-02

    High-quality and millimeter-sized perovskite single crystals of CsPbBr 3 and Cs 4 PbBr 6 were prepared in organic solvents and studied for correlation between photocurrent generation and photoluminescence (PL) emission. The CsPbBr 3 crystals, which have a 3D perovskite structure, showed a highly sensitive photoresponse and poor PL signal. In contrast, Cs 4 PbBr 6 crystals, which have a 0D perovskite structure, exhibited more than 1 order of magnitude higher PL intensity than CsPbBr 3 , which generated an ultralow photoresponse under illumination. Their contrasting optoelectrical characteristics were attributed to different exciton binding energies, induced by coordination geometry of the [PbBr 6 ] 4- octahedron sublattices. This work correlated the local structures of lead in the primitive perovskite and its derivatives to PL spectra as well as photoconductivity.

  11. 137Cs in the western South Pacific Ocean

    International Nuclear Information System (INIS)

    Yamada, Masatoshi; Wang Zhongliang

    2007-01-01

    The 137 Cs activities were determined for seawater samples from the East Caroline, Coral Sea, New Hebrides, South Fiji and Tasman Sea (two stations) Basins of the western South Pacific Ocean by γ spectrometry using a low background Ge detector. The 137 Cs activities ranged from 1.4 to 2.3 Bq m -3 over the depth interval 0-250 m and decreased exponentially from the subsurface to 1000 m depth. The distribution profiles of 137 Cs activity at these six western South Pacific Ocean stations did not differ from each other significantly. There was a remarkable difference for the vertical profiles of 137 Cs activity between the East Caroline Basin station in this study and the GEOSECS (Geochemical Ocean Sections Study) station at the same latitude in the Equatorial Pacific Ocean; the 137 Cs inventory over the depth interval 100-1000 m increased from 400 ± 30 Bq m -2 to 560 ± 30 Bq m -2 during the period from 1973 to 1992. The total 137 Cs inventories in the western South Pacific Ocean ranged from 850 ± 70 Bq m -2 in the Coral Sea Basin to 1270 ± 90 Bq m -2 in the South Fiji Basin. Higher 137 Cs inventories were observed at middle latitude stations in the subtropical gyre than at low latitude stations. The 137 Cs inventories were 1.9-4.5 times (2.9 ± 0.7 on average) and 1.7-4.3 times (3.1 ± 0.7 on average) higher than that of the expected deposition density of atmospheric global fallout at the same latitude and that of the estimated 137 Cs deposition density in 10 o latitude by 10 deg. longitude grid data obtained by Aoyama et al. [Aoyama M, Hirose K, Igarashi Y. Re-construction and updating our understanding on the global weapons tests 137 Cs fallout. J Environ Monit 2006;8:431-438], respectively. The possible processes for higher 137 Cs inventories in the western South Pacific Ocean than that of the expected deposition density of atmospheric global fallout may be attributable to the inter-hemisphere dispersion of the atmospheric nuclear weapons testing 137 Cs from

  12. Na/K pump inactivation, subsarcolemmal Na measurements, and cytoplasmic ion turnover kinetics contradict restricted Na spaces in murine cardiac myocytes.

    Science.gov (United States)

    Lu, Fang-Min; Hilgemann, Donald W

    2017-07-03

    Decades ago, it was proposed that Na transport in cardiac myocytes is modulated by large changes in cytoplasmic Na concentration within restricted subsarcolemmal spaces. Here, we probe this hypothesis for Na/K pumps by generating constitutive transsarcolemmal Na flux with the Na channel opener veratridine in whole-cell patch-clamp recordings. Using 25 mM Na in the patch pipette, pump currents decay strongly during continuous activation by extracellular K (τ, ∼2 s). In contradiction to depletion hypotheses, the decay becomes stronger when pump currents are decreased by hyperpolarization. Na channel currents are nearly unchanged by pump activity in these conditions, and conversely, continuous Na currents up to 0.5 nA in magnitude have negligible effects on pump currents. These outcomes are even more pronounced using 50 mM Li as a cytoplasmic Na congener. Thus, the Na/K pump current decay reflects mostly an inactivation mechanism that immobilizes Na/K pump charge movements, not cytoplasmic Na depletion. When channel currents are increased beyond 1 nA, models with unrestricted subsarcolemmal diffusion accurately predict current decay (τ ∼15 s) and reversal potential shifts observed for Na, Li, and K currents through Na channels opened by veratridine, as well as for Na, K, Cs, Li, and Cl currents recorded in nystatin-permeabilized myocytes. Ion concentrations in the pipette tip (i.e., access conductance) track without appreciable delay the current changes caused by sarcolemmal ion flux. Importantly, cytoplasmic mixing volumes, calculated from current decay kinetics, increase and decrease as expected with osmolarity changes (τ >30 s). Na/K pump current run-down over 20 min reflects a failure of pumps to recover from inactivation. Simulations reveal that pump inactivation coupled with Na-activated recovery enhances the rapidity and effectivity of Na homeostasis in cardiac myocytes. In conclusion, an autoregulatory mechanism enhances cardiac Na/K pump activity when

  13. New sulfido antimonates of the heavy alkali metals. Synthesis, crystal structure and chemical bonding of (K/Rb/Cs){sub 3}SbS{sub 3} and Cs{sub 3}SbS{sub 4} . H{sub 2}O; Neue Sulfido-Antimonate der schweren Alkalimetalle. Synthese, Kristallstruktur und chemische Bindung von (K/Rb/Cs){sub 3}SbS{sub 3} und Cs{sub 3}SbS{sub 4} . H{sub 2}O

    Energy Technology Data Exchange (ETDEWEB)

    Schindler, Lisa V.; Schwarz, Michael; Roehr, Caroline [Freiburg Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie

    2013-12-15

    The new sulfido antimonates(III) (Rb/Cs){sub 3}SbS{sub 3} were prepared from the alkali metal sulfides Rb{sub 2}S/Cs{sub 2}S{sub 2} and elemental antimony and sulfur or Sb{sub 2}S{sub 3} at reaction temperatures of about 700 C. The known isotypic potassium compound was similarly synthesized from the elements. The structures of the light-yellow crystals were refined using single-crystal X-ray data. Both compounds are isotypic to the respective Na salt forming the Na{sub 3}AsS{sub 3} structure type (cubic, space group P2{sub 1}3, K/Rb/Cs: a = 947.21(7)/982.28(5)/1025.92(5) pm, Z = 4, R1 = 0.0159/0.0560/0.0582). The {psi}-tetrahedral SbS{sub 3}{sup 3-} anions with Sb-S bond lengths of 242 pm are arranged in a cubic face centered packing, in which the three crystallographically different A{sup +} cations occupy the tetrahedral and octahedral voids, overall exhibiting a distorted octahedral sulfur coordination. The chemical bonding and the characteristics of the stereochemically active lone electron pair have been investigated by means of FP-LAPW band structure calculations. Needle-shaped crystals of the monohydrate of the antimony(V) salt Cs{sub 3}SbS{sub 4} . H{sub 2}O were obtained from a suspension of Sb{sub 2}O{sub 3}, CsOH and elemental sulfur. Cs{sub 3}SbS{sub 4} . H{sub 2}O crystallizes in a new structure type (monoclinic, space group P2{sub 1}/c, a = 987.17(10), b = 994.83(7), c = 1600.46(14) pm, {beta} = 126.895(8) , Z = 4, R1 = 0.0234). As expected, the Sb-S distances (233.1-234.7 pm) in the nearly ideally tetrahedral anion SbS{sub 4}{sup 3-} are considerably shorter than in the antimonates(III) but match the bond lengths in the anhydrous sulfido antimonate(V) Cs{sub 3}SbS{sub 4}. Due to their similar fcc-like anion packing and the stereochemically active lone electron pair of Sb in the antimonates(III), the whole series of compounds A{sub 3}Sb{sup III,V}S{sub 3/4} shows a uniform structure relation, which is elucidated using crystallographic group

  14. Effects of topical 0.2% Cyclosporine A on corneal neovascularization induced by xenologous amniotic membrane implantation into a corneal stroma micropocket of rats Efeitos do uso tópico da Ciclosporina A (CsA 0,2% na neovascularização corneal induzida pelo implante de membrana amniótica xenógena em microbolsa no estroma da córnea de ratos

    Directory of Open Access Journals (Sweden)

    Juliana F. Milani

    2008-08-01

    Full Text Available The objective of the study was to evaluate the topical effects of 0.2% Cyclosporine A (CsA on corneal neovascularization of rats following surgical implantation of equine amniotic membrane into a corneal stroma micropocket. The implantation of xenologous amniotic membrane was performed bilaterally in 90 rats. In the same day of the surgery each right eye started receiving topical CsA twice a day. The left eye received no medication and served as a control. The evaluation of corneal neovascularization was performed by computerized image analysis and histopathological evaluation at 1, 3, 7, 15, 30 and 60 days postoperatively. For the image analysis 10 animals were used per time period, and for the histopathological examination, five animals were used per time period. Image analysis found that corneal neovascularization began on the 3rd postoperative day, reached its peak on the 7th day, and then progressively and rapidly decreased. Statistic analysis indicated that neovascularization of the CsA treated eye on the 7th day was significantly higher than that observed in untreated eyes. On the 30th day, however, this pattern was reversed with the neovascularization observed in the CsA treated eyes declining to the low levels observed on the 3rd day. The degree of neovascularization in the untreated eyes on the 30th day declined to the baseline levels found on day 3 at the 60th day. Histopathological analysis indicated that deposition of collagen in the implanted tissue was completed by the 15th day. Therefore, we concluded that (1 equine amniotic membrane in rat corneal stroma produced an intense neovascularization until the 15th day postoperatively and then regressed, (2 deposition of collagen of the implanted tissue was completed on the 15th day postoperatively, and (3 use of CsA was associated with increase in the corneal neovascularization initially, followed by a quick and intense regression.Este estudo teve como objetivo a avaliação dos

  15. Sequestration and disposal of dissolved Cs+ using zeolite 13X

    Science.gov (United States)

    Park, M.; Park, J.; Jeong, H. Y.

    2017-12-01

    Low-to-intermediate level liquid radioactive wastes (LILLW) typically contain high levels of radioactive 137Cs. Due to the great radiational and thermal stability as well as the high selectivity, zeolite has been commonly utilized to sequester radioactive isotopes from nuclear wastewater effluents. In this study, an Al-rich synthetic zeolite 13X was evaluated for the sorption capacity of Cs+ as a function of pH (4.0-10.5), ionic strength (0.05 and 0.2 M), and initial Cs+ concentration (1×10-6-5×10-3 M). For safe disposal, Cs+-exchanged 13X was both thermally and hydrothermally treated under different temperature and pressure. Subsequently, the resultant materials were examined for the phase transition by X-ray diffraction (XRD) and the local coordination chemistry by X-ray absorption spectroscopy (XAS). Our experimental results will detail the Cs+ sorption behavior by 13X under varying solution compositions. Also, the structural changes of Cs+-exchanged 13X upon thermal and hydrothermal treatment will be delineated to assess the stability of Cs+ in the treated materials.

  16. Cs-137 in Arctic foxes (Alopex lagopus) on Svalbard

    International Nuclear Information System (INIS)

    Gwynn, Justin P.; Fuglei, Eva; Dowdall, Mark

    2007-01-01

    This study presents 137 Cs muscle activity concentrations in Arctic foxes (Alopex lagopus) from Svalbard over a period of several years and discusses the transfer of 137 Cs to Arctic foxes through likely predator-prey relationships. Mean 137 Cs activity concentrations and 137 Cs T ag values (per trapping season) ranged from 0.51 ± 2.76 to 1.32 ± 2.89 Bq/kg (w.w.) and 5.1 x 10 -4 to 1.3 x 10 -3 m 2 /kg, respectively. Mean concentration ratios of 137 Cs in Arctic foxes compared to probable prey ranged from 1.0 to 7.9. On Svalbard, transfer of 137 Cs to Arctic foxes is likely to occur via both marine and terrestrial food chains. The relative contribution of marine and terrestrial food sources to the diet of Arctic foxes may vary by location and by season and may lead to either an increase or decrease in the trophic transfer of 137 Cs to Arctic foxes compared to transfer resulting from terrestrial only diets

  17. Measurement limits to 134Cs concentration in soil

    International Nuclear Information System (INIS)

    Ahn, J.K.; Kim, J.S.; Lee, H.M.; Kim, H.; Kim, T.H.; Park, J.N.; Kang, Y.S.; Lee, H.S.; Kim, S.J.; Park, J.Y.; Ryu, S.Y.; Kim, H.-Ch.; Kang, W.G.; Kim, S.K.

    2011-01-01

    We investigate the caesium concentrations in soils in mountain areas near Gori nuclear power plant in Korea, focusing on the measurement limits to the 134 Cs. In order to lower the minimum detectable amount (MDA) of activity for the 134 Cs, we have used the ammonium molybdophosphate (AMP) precipitation method to get rid of the 40 K existing in natural radioactivity, which reduces the MDA activity about 10 times smaller than those without the AMP precipitation method. The MDA results for the 134 Cs were found to be in the range between 0.015 and 0.044 Bq/kg-dry weight. In order to diminish the background, we also have measured a part of the soil samples in Yangyang, a small town in the east coast of Korea. However, it turns out that in order to detect the 134 Cs in the samples the MDA should be reduced to the level of mBq/kg-dry weight. - Highlights: → We study the caesium concentrations in soils in mountain areas near Gori NPT in Korea. → We use the AMP precipitation method to lower the minimum detectable amount (MDA) of activity for the 134 Cs. → The results of the MDA for the 134 Cs turn out to be in the range between 0.015 and 0.044. → In order to detect the 134 Cs in the samples, the MDA should be reduced to the level of mBq/kg-dry weight.

  18. Measurement of 137Cs activity in living chicken

    International Nuclear Information System (INIS)

    Balas, J.; Poeschl, M.

    1998-01-01

    The possibility of measuring the 137 Cs activity in broiler chickens in vivo was examined. The experiment was conducted with broiler chickens 7 to 22 days old (White Leghorn hybrid, race ISA VEDETTE). Three oral doses of 137 Cs (total activity 5 kBq/chicken) were administered during a day (at 8:00, 12:00 and 16:00). The radioactivity was determined by gamma spectroscopy with a stabilised Nal/Tl detector. The measurement was carried out on days 1, 2, 3, 4, 7, 8, 14 and 15 after the 137 Cs administration in vivo. The detector was put closely to the body in the area of breast muscles. The radiocesium activity concentrations in fresh daily excreta were also determined. A rapid uptake of the orally administered 137 Cs (within a few hours) as well as a rapid loss of radiocesium were observed. The dynamics and accuracy of the in vivo measurement of 137 Cs activity were comparable with the recently published results of in vitro measurement of radiocesium activity. Only the initial 137 Cs activity (during 2 days after 137 Cs application) was higher with regard to the content of contaminated feed mixture in the gastrointestinal tract

  19. Chondroitin Sulfate (CS) Lyases: Structure, Function and Application in Therapeutics.

    Science.gov (United States)

    Rani, Aruna; Patel, Seema; Goyal, Arun

    2018-01-01

    Glycosaminoglycans (GAGs) such as chondroitin sulfate (CS) are the chief natural polysaccharides which reside in biological tissues mainly in extracellular matrix. These CS along with adhesion molecules and growth factors are involved in central nervous system (CNS) development, cell progression and pathogenesis. The chondroitin lyases are the enzyme that degrade and alter the CS chains and hence modify various signalling pathways involving CS chains. These CS lyases are substrate specific, can precisely manipulate the CS polysaccharides and have various biotechnological, medical and therapeutic applications. These enzymes can be used to produce the unsaturated oligosaccharides, which have immune-modulatory, anti-inflammatory and neuroprotective properties. This review focuses on the major breakthrough of the chondroitin sulfate degrading enzymes, their structures and functioning mechanism. This also provides comprehensive information regarding production, purification, characterization of CS lyases and their major applications, both established as well as emerging ones such as neural development. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.

  20. Waste forms based on Cs-loaded silicotitanates

    International Nuclear Information System (INIS)

    Balmer, M.L.; Bunker, B.C.

    1995-04-01

    Silicotitanate ion exchange materials are being considered for removal of radioactive Cs and Sr from tank wastes at the Hanford site. The phase evolution as a function of heat treatment temperature for several sol gel derived compositions within the Cs 2 O-SiO 2 -TiO 2 system was investigated, in order to determine if an adequate waste form can be achieved by direct thermal conversion. The Cs leach rates and Cs loss during heat treatment of select materials were measured. Some compositions which contain large amounts of Ti melt to form a glass with reasonably low aqueous leach rates. A new Cs-silicotitanate material with a structure isomorphous to pollucite was discovered. This material forms at low temperatures (700--800 C) where Cs volatility is negligible. The silicotitanate-pollucite exhibits extremely low leach rates (1.42 g/m 2 day ) at 90 C, and has been identified as a promising waste form for Cs containment

  1. Biotechnological potential of Azolla filiculoides for biosorption of Cs and Sr: Application of micro-PIXE for measurement of biosorption.

    Science.gov (United States)

    Ghorbanzadeh Mashkani, Saeid; Tajer Mohammad Ghazvini, Parisa

    2009-03-01

    The presence of Cs and Sr in culture medium of Azolla filiculoides caused about 27.4% and 46.3% inhibition of biomass growth, respectively, in comparison to A. filiculoides control weight which had not metals. Biosorption batch experiments were conducted to determine the Cs and Sr binding ability of native biomass and chemically modified biosorbents derived from Azolla namely ferrocyanide Azolla sorbents type 1 and type 2 (FAS1 and FAS2) and hydrogen peroxide Azolla sorbent (HAS). The best Cs and Sr removal results were obtained when A. filiculoides was treated by 2M MgCl(2) and 30ml H(2)O(2) 8mM at pH 7 for 12h and it was then washed by NaOH solution at pH 10.5 for 6h. Pretreatment of Azolla have been suggested to modify the surface characteristics which could improve biosorption process. The binding of Cs and Sr on the cell wall of Azolla was studied with micro-PIXE and FT-IR.

  2. 134Cs emission probabilities determination by gamma spectrometry

    Science.gov (United States)

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

    2018-03-01

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

  3. Study of /sup 137/Cs absorption by Lemna minor

    Energy Technology Data Exchange (ETDEWEB)

    Bergamini, P G; Palmas, G; Piantelli, F; Sani, M [Siena Univ. (Italy). Ist. di Fisica; Banditelli, P; Previtera, M; Sodi, F

    1979-09-01

    Absorption of /sup 137/Cs by the floating aquatic plant Lemna minor in relation to /sup 137/Cs concentration in the water was measured under controlled conditions of temperature, pH and light. The method used to analyse the results is described. When applied to this study the method shows the influence on /sup 137/Cs absorption of (1) potassium-cesium exchange due to chemical affinity, (2) the natural colony growth of the organism and (3) the effect of light. Concentration factors were determined for these three processes.

  4. Study of 137Cs absorption by Lemna minor

    International Nuclear Information System (INIS)

    Bergamini, P.G.; Palmas, G.; Piantelli, F.; Sani, M.; Banditelli, P.; Previtera, M.; Sodi, F.

    1979-01-01

    Absorption of 137 Cs by the floating aquatic plant Lemna Minor in relation to 137 Cs concentration in the water was measured under controlled conditions of temperature, pH and light. The method used to analyse the results is described. When applied to this study the method shows the influence on 137 Cs absorption of (1) potassium-cesium exchange due to chemical affinity, (2) the natural colony growth of the organism and (3) the effect of light. Concentration factors were determined for these three processes. (author)

  5. New aluminium-rich alkali slag matrix with clay minerals for immobilizing simulated radioactive Sr and Cs waste

    International Nuclear Information System (INIS)

    Qian Guangren; Sun, Darren Delai; Tay, Joo Hwa

    2001-01-01

    A new aluminium-rich alkali-activated slag matrix (M-AAS) with clay absorbents has been developed for immobilization of simulated radioactive Sr or Cs waste by introducing metakaolin, natural zeolite and NaOH-treated attapulgite clay minerals into alkali-activated slag matrix (AAS). The results revealed that the additions of metakaolin and clay absorbents into the cementitious matrixes would greatly enhance the distribution ratio, R d , of selective adsorption whether the matrix was OPC matrix or AAS matrix. The new immobilizing matrix M-AAS not only exhibited the strongest selective adsorption for both Sr and Cs ions, but also was characterized by lower porosity and small pore diameter so that it exhibited the lowest leaching rate. Hydration product analyses also demonstrated that (Na+Al)-substituted C-S-H(I) and self-generated zeolite were major hydration products in the M-AAS matrix, which provided this new immobilizing matrix with better selective adsorption on Sr and Cs and lower leaching rate

  6. Changing US Attributes After CS-US Pairings Changes CS-Attribute-Assessments: Evidence for CS-US Associations in Attribute Conditioning.

    Science.gov (United States)

    Förderer, Sabine; Unkelbach, Christian

    2016-03-01

    Attribute Conditioning (AC) refers to people's changed assessments of stimuli's (CSs) attributes due to repeated pairing with stimuli (USs) possessing these attributes; for example, when an athletic person (US) is paired with a neutral person (CS), the neutral person is judged to be more athletic after the pairing. We hypothesize that this AC effect is due to CSs' associations with USs rather than direct associations with attributes. Three experiments test this hypothesis by changing US attributes after CS-US pairings. Experiments 1 and 2 conditioned athleticism by pairing neutral men (CSs) with athletic and non-athletic USs. Post-conditioning, USs' athleticism was reversed, which systematically influenced participants' assessment of CS athleticism. Experiment 3 conditioned athleticism and changed USs' musicality after CS-US pairings. This post-conditioning change affected musicality assessments of CSs but did not influence athleticism-assessments. The results indicate that AC effects are based on an associative CS-US-attribute structure. © 2016 by the Society for Personality and Social Psychology, Inc.

  7. Cs-selective mineral adsorbents in columns: physico-chemical properties and modeling

    International Nuclear Information System (INIS)

    Michel, Caroline

    2015-01-01

    Following the nuclear disaster in Fukushima Dai-Ichi, thousands of tons of fresh water and seawater were used for cooling the reactors or contaminated as a result of groundwater seepage. Decontamination of these waters is complicated by the presence of other cations (Na + , K + , Ca 2+ , Mg 2+ ) naturally present in these waters. Decontamination process in columns packed was studied in this context with two types of mineral adsorbents: the TERMOXID 35 and the SORBMATECH 202. The first one is a commercial adsorbent and consists of mixed ferrocyanide K/Ni impregnated over a solid matrix Zr(OH) 4 . The second one was synthesized in CEA and is composed of ferrocyanide K/Cu impregnated over a solid matrix SiO 2 . Both materials have shown a high efficiency for Cs decontamination in seawater with K(d,Cs) of about 10 5 mL/g. Batch studies conducted in different solutions (pure water, fresh water and seawater) allowed determining sorption kinetics and ion exchange mechanisms responsible for the sorption of Cs + , taking into account competitive effects of the natural water cations (Na + , K + , Ca 2+ , Mg 2+ ). Modelling of batches was performed with the geochemical code CHESS considering competitive effects according to the Vanselow formalism and selectivity coefficients, developing a specific thermodynamic database. The performances of these materials were then tested in column. The operating parameters such as Darcy's velocity and the H/D ratio were studied for a proper functioning of this process. The T35 has proven to be less efficient mainly because of the slow diffusion of Cs in the pores of the material. The S 2 O 2 has proven to be a good candidate for the application of high flow rates. The breakthrough curves obtained in fresh water have been modelled with the reactive transport codes HYTEC and OPTIPUR using the CHESS thermodynamic database. This approach will eventually help to support the design of a decontamination unit by the operator. (author) [fr

  8. A novel vanadosilicate with hexadeca-coordinated Cs{sup +} ions as a highly effective Cs{sup +} remover

    Energy Technology Data Exchange (ETDEWEB)

    Datta, Shuvo Jit; Moon, Won Kyung; Choi, Do Young; Hwang, In Chul; Yoon, Kyung Byung [Sogang Univ., Seoul (Korea, Republic of). Korea Center for Artificial Photosynthesis

    2014-07-07

    The effective removal of {sup 137}Cs{sup +} ions from contaminated groundwater and seawater and from radioactive nuclear waste solutions is crucial for public health and for the continuous operation of nuclear power plants. Various {sup 137}Cs{sup +} removers have been developed, but more effective {sup 137}Cs{sup +} removers are still needed. A novel microporous vanadosilicate with mixed-valence vanadium (V{sup 4+} and V{sup 5+}) ions is now reported, which shows an excellent ability for Cs{sup +} capture and immobilization from groundwater, seawater, and nuclear waste solutions. This material is superior to other known materials in terms of selectivity, capacity, and kinetics, and at very low Cs{sup +} concentrations, it was found to be the most effective material for the removal of radioactive Cs{sup +} ions under the test conditions. This novel vanadosilicate also contains hexadeca-coordinated Cs{sup +} ions, which corresponds to the highest coordination number ever described.

  9. Bio-geochemical behavior of 90Sr, 137Cs and 60Co in tropical soil

    International Nuclear Information System (INIS)

    Wasserman, M.A.; Gonzales Viana, A.; Bartoly, F.; Carvalho Conti, C. de; Janvrot Vivone, R.; Perez, V.; Wasserman, J.C.

    2004-01-01

    One manner to assess the bio-geochemical behavior of radionuclides in soils is the integration of experimental methods results obtained in the laboratory with results obtained in field experiments. In this work was used an alternative sequential chemical extraction protocol to evaluate mobility of radionuclides as a function of some physico-chemical conditions operationally defined: Slightly acidic phase: CH 3 COOH + CH 3 COONa 1:1, pH 4.7, shacked at room temperature; Easily reducible phase: NH 2 OH.HCl (0.1 M), pH 2, shacked at room temperature;Oxidizable phase: H 2 O 2 (30%) + HNO 3 , pH 2, CH 3 COONH 4 (1 M);shacked at room temperature; Alkaline phase: NaOH (0.1 M), pH 12, shacked at room temperature; Resistant phase: Aqua regia heated to 50 deg C / 30 min. The results obtained experimentally indicate the vulnerability of some Brazilian soils due to the higher radionuclide transfer to plant. Although it seems clear that it is difficult to identify which soil property will determine a given TF, the results of geochemical partition for 137 Cs, 90 Sr and 60 Co obtained in slightly acidic phase were very consistent with the TF data for reference plants or with some of the soil properties recognized in the specialized literature as related with mechanisms of sorption of Cs (e.g. exchangeable K, organic matter and iron oxides content), Co (e.g. manganese oxide) and Sr (pH and exchangeable Ca). The 137 Cs distribution in soil showed that Fe oxides are the main sink for this element in all type of soil and 16 years after contamination the 137 Cs the TF remains almost the same in Goiania soil. The 60 Co distribution in soil showed that Mn oxides are the main sink for this element in all type of soils and in the Nitisol, 5 years after contamination, the 60 Co was not detected as bioavailable (in the slightly acidic phase) neither detected in plant or were detectable with values very close to the detection limit. In the Nitisol, it is possible that reduction in 137 Cs

  10. Characteristics of Pb{sup 2+} doped CsI matrix under gamma and neutron excitations

    Energy Technology Data Exchange (ETDEWEB)

    Pereira, Maria da Conceição Costa; Madi Filho, Tufic; Berretta, José Roberto; Tomaz, Lucas Faustino; Pinto, Marlene Cristina, E-mail: macoper@ipen.br, E-mail: tmfilho@ipen.br, E-mail: jrretta@ipen.br, E-mail: lucasfaus@gmail.com, E-mail: tynapinto@gmail.com [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2017-07-01

    In recent years, there has been an increasing interest in finding new fast scintillating material or improve the characteristics of known scintillators for the demand of high energy physics, industrial and nuclear medical applications. Ions divalent lead Pb{sup 2+} built in some crystal structures are efficient emission centers and their applications in scintillators was and still is the reason of an intensive study of emission properties of different compounds containing these ions. The aggregation of impurities in CsI is poorly studied. The problem of impurity aggregation in CsI is of interest from point of view of the luminescent properties modification of this scintillation material. In this context, the crystals of Pb{sup 2+} doped CsI matrix were grown by the vertical Bridgman technique and subjected to annealing in vacuum of 10{sup -6} mbar and continuous temperature of 350°C, for 24 hours, and then they were employed. To evaluate the response of the CsI:Pb scintillator crystal to gamma radiation, radioactive sources of {sup 137}Cs (662 keV), {sup 60}Co (1173 keV and 1333 keV), {sup 22}Na (511 keV and 1275 keV) and {sup 13}3Ba (355 keV) was used. The operating voltage of the photomultiplier was 2700 V for the detection of gamma rays and the accumulation time in the counting process was 600 s. The crystals used in gamma spectroscopy were cut with dimensions of 20 mm in diameter and 20 mm in height. The scintillator response to neutron radiation from a radioactive source of Am/Be with energy range of 1 MeV to 12 MeV was available. The activity of the AmBe source was 1Ci Am. The fluency was 2.6 x 10{sup 6} neutrons / second. The operating voltage of the photomultiplier tube was 1300 V. The accumulation time in the counting process was 600 s. The scintillator crystals were cut with dimensions of 20 mm diameter and 10 mm height. With the results obtained, it may be observed that the crystals are sensitive to these radiations. (author)

  11. Facile synthesis of NaYF4:Yb, Ln/NaYF4:Yb core/shell upconversion nanoparticles via successive ion layer adsorption and one-pot reaction technique

    NARCIS (Netherlands)

    Zeng, Q.; Xue, B.; Zhang, Y.; Wang, D.; Liu, X.; Tu, L.; Zhao, H.; Kong, X.; Zhang, H.

    2013-01-01

    The facile one-pot synthesis of NaYF4:Yb, Ln/NaYF4:Yb core/shell (CS) upconversion nanoparticles (UCNPs) was firstly developed through the successive ion layer adsorption and reaction (SILAR) technique, which represents an attractive alternative to conventional synthesis utilizing the chloride of Ln

  12. Hybridization of Single Nanocrystals of Cs4PbBr6 and CsPbBr3

    OpenAIRE

    Weerd, Chris de; Lin, Junhao; Gomez, Leyre; Fujiwara, Yasufumi; Suenaga, Kazutomo; Gregorkiewicz, Tom

    2017-01-01

    Nanocrystals of all-inorganic cesium lead halide perovskites (CsPbX3, X = Cl, Br, I) feature high absorption and efficient narrow-band emission which renders them promising for future generation of photovoltaic and optoelectronic devices. Colloidal ensembles of these nanocrystals can be conveniently prepared by chemical synthesis. However, in the case of CsPbBr3, its synthesis can also yield nanocrystals of Cs4PbBr6 and the properties of the two are easily confused. Here, we investigate in de...

  13. Načrtovan porod na domu

    OpenAIRE

    Todorović, Tamara; Takač, Iztok

    2017-01-01

    Izhodišča: Porod na domu je sicer star toliko kot človeštvo, pa vendar v veliki večini srednje in visoko razvitih držav prevladuje mnenje, da so zaradi nepredvidljivosti zapletov porodnišnice najbolj varno okolje za rojevanje. Kljub temu obstaja peščica držav, v katerih je porod na domu integriran v sistem zdravstvenega varstva (npr. Nizozemska, Velika Britanija, Kanada). Pri porodih na domu ločimo nenačrtovane in načrtovane porode na domu, slednje pa lahko nadalje razdelimo še na porode s sp...

  14. Plutonium isotopes/137Cs activity ratios for soil in Montenegro

    International Nuclear Information System (INIS)

    Antovic, N. M.; Vukotic, P.; Svrkota, N.; Andrukhovich, S.K.

    2011-01-01

    Plutonium isotopes/ 137 Cs activity ratios were determined for six soil samples from Montenegro, using the results of alpha-spectrometric measurements of 239+240 Pu and 238 Pu, as well as gamma-spectrometric cesium measurements. An average 239+240 Pu/ 137 Cs activity ratio is found to be 0.02, as the 238 Pu/ 137 Cs and 238 Pu/ 239+240 Pu one - 0.0006 and 0.03, respectively. It follows from the results that the source of plutonium in Montenegro soil is nuclear weapon testing during the fifties and sixties of the twentieth century. On the other hand, there is a contribution of the accident at the Chernobyl nuclear power plant to the soil contamination with 137 Cs isotope. [sr

  15. Speciation of 137Cs in the Baltic sea water

    International Nuclear Information System (INIS)

    Lujaniene, G.; Morkuniene, R.; Styra, D.

    1998-01-01

    A possibility of application of Filtrac 391 and Nuclepore filters, Ky-2-8-C exchanger and the Mtilon-T fiber impregnated with Fe, Co, Ni ferrocyanides for separation of particulate and ionic 137 Cs in the sea water was investigated. Physico-chemical forms of 137 Cs were investigated in the Baltic Sea water during 1995-1997. It was determined that 137 Cs was mainly present in ionic form (62-93 %) both in the near-shore and open waters. Concentration of particulate 137 Cs ranged from 255 to 625 Bq/kg (dry weight).The distribution coefficient (K d ) of radiocaesium reached values of 2100-9700. (author)

  16. Quasi-freestanding graphene on Ni(111) by Cs intercalation

    KAUST Repository

    Alattas, Maha Hassan Mohssen; Schwingenschlö gl, Udo

    2016-01-01

    A possible approach to achieve quasi-freestanding graphene on a substrate for technological purpose is the intercalation of alkali metal atoms. Cs intercalation between graphene and Ni(111) therefore is investigated using density functional theory

  17. Quasi-freestanding graphene on Ni(111) by Cs intercalation

    KAUST Repository

    Alattas, Maha Hassan Mohssen; Schwingenschlö gl, Udo

    2017-01-01

    It is of technological interest to achieve quasi-freestanding graphene on a substrate. A possible approach is the intercalation of alkali metal atoms. Cs intercalation between graphene and Ni(111) is investigated using density functional theory

  18. Kinetics of Cs adsorption on soils with different mineralogical composition

    International Nuclear Information System (INIS)

    Nakao, Atsushi; Funakawa, Shinya; Kosaki, Takashi

    2004-01-01

    137 Cs is one of the main radioisotopes released into the environment by nuclear powerstation accidents (e.g. Chernobyl) and nuclear weapons tests. Many studies have shown that Cs tends to remain at surface soils due to the high adsorption selectivity of clay minerals for this element. This behavior of the Cs + ion is, however, assumed to vary significantly depending on the mineralogical composition of the soil. The main objective of this study is to analyze the kinetics of Cs adsorption on soils with different mineralogical composition. Soil samples used in this study were Mollisols (Um) and Alfisols (Ua) from Ukraine, Ultisols (Tu) from Thailand and Spodosols (Js) from Japan. The dominant clay species of these soils are montmorillonite (Um, Ua), kaolinite and mica (Tu) and beidellite (Js). The rates of Cs adsorption and Ca or K desorption were measured using a continuous flow method. Soil samples that were previously saturated with Ca 2+ were leached with a 0.75 mmol/l Cs + solution at a constant rate of 2.0 ml/min. The leachate was collected every 10 minutes and the concentrations of Cs + , Ca 2+ and K + of each aliquot were measured by atomic adsorption spectrophotometry (Cs + , Ca 2+ ) and flame spectrophotometry (K + ). The datasets obtained were simulated using the first order kinetic model: y = a(1 - exp(-kt)), where a is the adsorption (desorption) maximum and k the rate constant. It is here assumed that Ca 2+ is desorbed from cation exchange sites and K + desorbed from the frayed edges of micaceous minerals. The values of a obtained for both Cs adsorption and Ca desorption was in the order Js>Um>Tu>Ua, whereas the values of k were in the order Tu>Ua>Um>Js. This result reflects the values of permanent negative charge of clays which are originated from the substitution of cations in the structure of 2:1 clay minerals. The value of a for K + desorption was, however, highest in Tu, suggesting that the values of Cs + -exchangeable K + correspond to the amount

  19. Radiological Cs-137 accidents/incidents in Estonia

    International Nuclear Information System (INIS)

    Sinisso, Mark

    1997-01-01

    Two radiological accidents/incidents in Estonia are reported. The first -21 October 1994, three brothers entered the Tammiku repository and stole a radioactive Cs-137 source and received dangerous doses of radiation. The other incident (early 1995) involved an abandoned source - a discarded metal cylinder containing Cs-137. Chronologies and factual data are considered for both events. Concise descriptions of the incidents, a medical overview of the fate of injured people and lessons learned are presented

  20. Radiological Cs-137 accidents/incidents in Estonia

    Energy Technology Data Exchange (ETDEWEB)

    Sinisso, Mark [Ministry of Foreign Affairs, Tallin (Estonia)

    1997-12-31

    Two radiological accidents/incidents in Estonia are reported. The first -21 October 1994, three brothers entered the Tammiku repository and stole a radioactive Cs-137 source and received dangerous doses of radiation. The other incident (early 1995) involved an abandoned source - a discarded metal cylinder containing Cs-137. Chronologies and factual data are considered for both events. Concise descriptions of the incidents, a medical overview of the fate of injured people and lessons learned are presented

  1. Detection of CS in Neptune's atmosphere from ALMA observations

    Science.gov (United States)

    Moreno, R.; Lellouch, E.; Cavalié, T.; Moullet, A.

    2017-12-01

    Context. The large and vertically non-uniform abundance of CO in Neptune's atmosphere has been interpreted as the result of past cometary impact(s), either single or distributed in size and time, which could also be at the origin of Neptune's HCN. Aims: We aim to provide observational support for this scenario by searching for other comet-induced species, in particular carbon sulfide (CS) which has been observed continuously in Jupiter since the 1994 Shoemaker-Levy 9 impacts. Methods: In April 2016 we used the ALMA interferometer to search for CS(7-6) at 342.883 GHz in Neptune. Results: We report on the detection of CS in Neptune's atmosphere, the first unambiguous observation of a sulfur-bearing species in a giant planet beyond Jupiter. Carbon sulfide appears to be present only at submillibar levels, with a column density of (2.0-3.1) × 1012 cm-2, and a typical mixing ratio of (2-20) × 10-11 that depends on its precise vertical location. The favoured origin of CS is deposition by a putative large comet impact several centuries ago, and the strong depletion of CS with respect to CO - compared to the Jupiter case - is likely due to the CS sticking to aerosols or clustering to form polymers in Neptune's lower stratosphere. Conclusions: The CS detection, along with recent analyses of the CO profile, reinforces the presumption of a large comet impact into Neptune 1000 yr ago, that delivered CO, CS, and HCN at the same time.

  2. 137Cs content in edible mushrooms of the Transcarpathian region

    Directory of Open Access Journals (Sweden)

    O. O. Parlag

    2013-03-01

    Full Text Available Edible mushrooms (Boletus edulis Bull.: Fr. and Leccinum scabrum (Bull.: Fr. S.F.Gray of Transcarpathian region were analyzed on content of 137Cs. Specific activity of 137Cs in collected mushrooms did not exceed 354 ± 53 Bq/kg (dry substance. Estimation of the contribution into internal exposure dose of population for the condi-tion of 1 kg of mushrooms consumption is carried out.

  3. 137Cs radioactive dating of Lake Ontario sediment cores

    International Nuclear Information System (INIS)

    Ward, T.E.; Breeden, J.; Komisarcik, K.; Porter, R.; Czuczwa, J.; Kaminski, R.; McVeety, B.D.

    1987-12-01

    The distribution of 137 Cs in sediment cores from Lake Ontario provides estimates of the sediment accumulation rates. Geochronology with 210 Pb dating and distribution of Ambrosia (ragweed) pollen compare well with 137 Cs dating. These methods can determine with precision, changes in sedimentation occurring over the past 100 years or so. Typical sedimentation rates of 0.18-0.36 cm/yr were measured. 16 refs., 3 figs., 2 tabs

  4. Obsah Cs-137 v houbách

    OpenAIRE

    ČADOVÁ, Michaela

    2015-01-01

    The aim of this work is to compare the presence of Cs-137 in different kinds of mushrooms in selected locations using semiconductor gamma-ray spectrometry. Research question was determined: Does Cs-137 content amount vary depending on the fungal species? The first part deals with basic knowledge of ionizing radiation, which is important for the complex understanding of thematic problems. This concerns basic radiobiological terms such as radioactivity, ionizing radiation, its biological effect...

  5. Distribution of Alkalis (Na, Cs, Rb) Between Silicate and Sulfide: Implications for Planetary Volatile Depletion

    Science.gov (United States)

    Boujibar, A.; Fei, Y.; Righter, K.; Du, Z.; Bullock, E.

    2018-01-01

    The abundances of volatile elements in the Earth's mantle are correlated with their temperatures of condensation. This depletion can be due to either incomplete condensation of the elements during the nebula condensation or evaporation processes during planetary growth. Elements that have affinities with metals (siderophile) and sulfides (chalcophile) are additionally depleted due to their segregation into the core. Therefore, study of lithophile elements could be useful to isolate processes of volatilization and their effect on the abundance of the elements in the Earth's mantle. However, the correlation of these lithophile elements including alkali elements, with their temperatures of condensation shows a significant scatter, which is difficult to reconcile with a depletion by vaporization or incomplete condensation alone.

  6. Bioaccumulation of 137Cs and 60Co by Helianthus annuus

    International Nuclear Information System (INIS)

    Hornik, M.; Pipiska, M.; Vrtoch, L.; Augustin, J.; Lesny, J.

    2005-01-01

    The 60 Co and 137 Cs bioaccumulation by Helianthus annuus L. was measured during 9 day cultivation at 20 ± 2 o C in hydroponic Hoagland medium. Previous starvation for K + and for NH 4 + 2.2 and 2.7 times, respectively, enhanced 137 Cs uptake rate. Previous cultivation in surplus of K + ions 50 mmol·l -1 has no effect on 137 Cs bioaccumulation rate. Both 137 Cs and 60 Co bioaccumulation significantly increase with dilution of basic Hoagland medium up to 1:7 for caesium and up to 1:3 for cobalt followed by mild decrease at higher dilutions. Root to shoot specific 137 Cs radioactivity ratio (Bq.g -1 /Bq·g -1 , fresh wt.) increased with dilution from 1.46 to 9.6-9.8. The values root to shoot specific radioactivity ratio for 60 Co were less dependent on the nutrient concentrations and were within the range 5.7 to 8.5. 137 Cs was localized mainly in young leaves (30%) and roots (39%) and 60 Co mainly in roots (67%) and leaves (20%). Obtained data showed less sensitivity of 60 Co uptake by sunflower on nutrient concentration in hydroponic media. (author)

  7. Performance verification tests of JT-60SA CS model coil

    Energy Technology Data Exchange (ETDEWEB)

    Obana, Tetsuhiro, E-mail: obana.tetsuhiro@LHD.nifs.ac.jp [National Institute for Fusion Science, 322-6 Oroshi, Toki, Gifu 509-5292 (Japan); Murakami, Haruyuki [Japan Atomic Energy Agency, 801-1 Mukoyama, Naka, Ibaraki 311-0193 (Japan); Takahata, Kazuya; Hamaguchi, Shinji; Chikaraishi, Hirotaka; Mito, Toshiyuki; Imagawa, Shinsaku [National Institute for Fusion Science, 322-6 Oroshi, Toki, Gifu 509-5292 (Japan); Kizu, Kaname; Natsume, Kyohei; Yoshida, Kiyoshi [Japan Atomic Energy Agency, 801-1 Mukoyama, Naka, Ibaraki 311-0193 (Japan)

    2015-11-15

    Highlights: • The performance of the JT-60SA CS model coil was verified. • The CS model coil comprised a quad-pancake wound with a Nb{sub 3}Sn CIC conductor. • The CS model coil met the design requirements. - Abstract: As a final check of the coil manufacturing method of the JT-60 Super Advanced (JT-60SA) central solenoid (CS), we verified the performance of a CS model coil. The model coil comprised a quad-pancake wound with a Nb{sub 3}Sn cable-in-conduit conductor. Measurements of the critical current, joint resistance, pressure drop, and magnetic field were conducted in the verification tests. In the critical-current measurement, the critical current of the model coil coincided with the estimation derived from a strain of −0.62% for the Nb{sub 3}Sn strands. As a result, critical-current degradation caused by the coil manufacturing process was not observed. The results of the performance verification tests indicate that the model coil met the design requirements. Consequently, the manufacturing process of the JT-60SA CS was established.

  8. Performance Evaluation of the Sysmex CS-5100 Automated Coagulation Analyzer.

    Science.gov (United States)

    Chen, Liming; Chen, Yu

    2015-01-01

    Coagulation testing is widely applied clinically, and laboratories increasingly demand automated coagulation analyzers with short turn-around times and high-throughput. The purpose of this study was to evaluate the performance of the Sysmex CS-5100 automated coagulation analyzer for routine use in a clinical laboratory. The prothrombin time (PT), international normalized ratio (INR), activated partial thromboplastin time (APTT), fibrinogen (Fbg), and D-dimer were compared between the Sysmex CS-5100 and Sysmex CA-7000 analyzers, and the imprecision, comparison, throughput, STAT function, and performance for abnormal samples were measured in each. The within-run and between-run coefficients of variation (CV) for the PT, APTT, INR, and D-dimer analyses showed excellent results both in the normal and pathologic ranges. The correlation coefficients between the Sysmex CS-5100 and Sysmex CA-7000 were highly correlated. The throughput of the Sysmex CS-5100 was faster than that of the Sysmex CA-7000. There was no interference at all by total bilirubin concentrations and triglyceride concentrations in the Sysmex CS-5100 analyzer. We demonstrated that the Sysmex CS-5100 performs with satisfactory imprecision and is well suited for coagulation analysis in laboratories processing large sample numbers and icteric and lipemic samples.

  9. Cs-137 and Sr-90 level in diary products

    International Nuclear Information System (INIS)

    Petukhov, V.L.; Dukhanov, Y.A.; Sevryuk, I.Z.; Patrashkov, S.A.; Korotkevich, O.S.; Gorb, T.S.; Petukhov, I.V.

    2003-01-01

    About 70% of radioactive substances fell on the territory of the Byelorussian Republic after the Chernobyl Atom Power Station Disaster. Cs-137 and Sr-90 accumulation dynamics was studied in milk of the cows from the highest polluted Braginsky area. 408 milk samples of Black and White cows were investigated. In 1995 average Cs-137 and Sr-90 levels were 61.00 and 3.73 Bk/dm 3 respectively. Cs-137 and Sr-90 levels exceeded Byelorussian Republic upper limits RDU - 96 in 10 and 50% of milk samples respectively. After 5 years (by 2000) Cs-137 and Sr-90 levels had become almost 3 and 2 times less (21.70 Bk/dm 3 and 1.72 Bk/dm 3 respectively). Cs-137 and Sr-90 levels exceeded RDU - 96 in 1.5 and 5.5% of milk samples respectively. In the same periods Cs-137 and Sr-90 levels were 7 and 2 times higher than the similar indexes in the relatively clean Novosibirsk area. Thus, radioactive element levels in milk of Black and White cows of the Byelorussian Republic decreased significantly for the past years. (authors)

  10. Transfer of 137Cs through the food chain to man

    International Nuclear Information System (INIS)

    Evans, C.; Bennett, B.G.

    1976-10-01

    Deposition, concentrations in diet, and body burdens of 137 Cs have been measured since 1954 at various sites throughout the world. This report is a compilation and updating of various fallout 137 Cs measurements and an interpretation of transfer properties of 137 Cs from deposition to diet and from diet to man. An empirical model is used to correlate deposition and diet data. Direct foliar contamination, stored food supplies, and uptake from soil contribute to the dietary levels of 137 Cs. The accumulation of 137 Cs by man is described by a single exponential model. The inferred biological half-times, 200 to 400 days, are somewhat greater than the half-time of about 100 days obtained from shorter term studies. Differences in body burdens due to sex, age, and weight are discussed. During the period 1954 to 1974, the internal dose from fallout 137 Cs, based on average body burdens, is estimated to be 4 to 5 percent of the 21 year radiation dose from 40 K

  11. The Two Translationally Controlled Tumor Protein Genes, CsTCTP1 and CsTCTP2, Are Negative Modulators in the Cucumis sativus Defense Response to Sphaerotheca fuliginea

    Directory of Open Access Journals (Sweden)

    Xiangnan Meng

    2018-04-01

    Full Text Available Pathogen stress often significantly decreases cucumber production. However, knowledge regarding the molecular mechanism and signals of cucumber disease resistance is far from complete. Here, we report two translationally controlled tumor protein genes, CsTCTP1 and CsTCTP2, that are both negative modulators in the Cucumis sativus defense response to Sphaerotheca fuliginea. Subcellular localization analysis showed that CsTCTP1 and CsTCTP2 were both localized in the cytoplasm. Expression analysis indicated that the transcript levels of CsTCTP1 and CsTCTP2 were linked to the degree of cucumber resistance to S. fuliginea. Transient overexpression of either CsTCTP1 or CsTCTP2 in cucumber cotyledons impaired resistance to S. fuliginea, whereas silencing of either CsTCTP1 or CsTCTP2 enhanced cucumber resistance to S. fuliginea. The relationship of several defense-related genes and ABA and target of rapamycin (TOR signaling pathway-related genes to the overexpressing and silencing of CsTCTP1/CsTCTP2 in non-infested cucumber plants was investigated. The results indicated that CsTCTP1 participates in the defense response to S. fuliginea by regulating the expression of certain defense-associated genes and/or ABA signaling pathway-associated genes, and CsTCTP2 participates through regulating the expression of TOR signaling pathway-associated genes. Our findings will guide enhancing the resistance of cucumber to powdery mildew.

  12. The distribution of {sup 137}Cs, K, Rb and Cs in plants in a Sphagnum-dominated peatland in eastern central Sweden

    Energy Technology Data Exchange (ETDEWEB)

    Vinichuk, M., E-mail: mykhailo.vinichuk@mark.slu.s [Department of Soil and Environment, Swedish University of Agricultural Sciences, SLU, P.O. Box 7014, SE-750 07 Uppsala (Sweden); Department of Ecology, Zhytomyr State Technological University, 103 Chernyakhovsky Street, 10005 Zhytomyr (Ukraine); Johanson, K.J. [Department of Soil and Environment, Swedish University of Agricultural Sciences, SLU, P.O. Box 7014, SE-750 07 Uppsala (Sweden); Rydin, H. [Department of Plant Ecology, Evolutionary Biology Centre, Uppsala University, Norbyvaegen 18D, SE-752 36 Uppsala (Sweden); Rosen, K. [Department of Soil and Environment, Swedish University of Agricultural Sciences, SLU, P.O. Box 7014, SE-750 07 Uppsala (Sweden)

    2010-02-15

    We record the distribution of {sup 137}Cs, K, Rb and Cs within individual Sphagnum plants (down to 20 cm depth) as well as {sup 137}Cs in vascular plants growing on a peatland in eastern central Sweden. In Calluna vulgaris{sup 137}Cs was mainly located within the green parts, whereas Andromeda polifolia, Eriophorum vaginatum and Vaccinium oxycoccos showed higher {sup 137}Cs activity in roots. Carex rostrata and Menyanthes trifoliata showed variable distribution of {sup 137}Cs within the plants. The patterns of {sup 137}Cs activity concentration distribution as well as K, Rb and Cs concentrations within individual Sphagnum plants were rather similar and were usually highest in the capitula and/or in the subapical segments and lowest in the lower dead segments, which suggests continuous relocation of those elements to the actively growing apical part. The {sup 137}Cs and K showed relatively weak correlations, especially in capitula and living green segments (0-10 cm) of the plant (r = 0.50). The strongest correlations were revealed between {sup 137}Cs and Rb (r = 0.89), and between {sup 137}Cs and stable Cs (r = 0.84). This suggests similarities between {sup 137}Cs and Rb in uptake and relocation within the Sphagnum, but that {sup 137}Cs differs from K.

  13. The distribution of 137Cs, K, Rb and Cs in plants in a Sphagnum-dominated peatland in eastern central Sweden

    International Nuclear Information System (INIS)

    Vinichuk, M.; Johanson, K.J.; Rydin, H.; Rosen, K.

    2010-01-01

    We record the distribution of 137 Cs, K, Rb and Cs within individual Sphagnum plants (down to 20 cm depth) as well as 137 Cs in vascular plants growing on a peatland in eastern central Sweden. In Calluna vulgaris 137 Cs was mainly located within the green parts, whereas Andromeda polifolia, Eriophorum vaginatum and Vaccinium oxycoccos showed higher 137 Cs activity in roots. Carex rostrata and Menyanthes trifoliata showed variable distribution of 137 Cs within the plants. The patterns of 137 Cs activity concentration distribution as well as K, Rb and Cs concentrations within individual Sphagnum plants were rather similar and were usually highest in the capitula and/or in the subapical segments and lowest in the lower dead segments, which suggests continuous relocation of those elements to the actively growing apical part. The 137 Cs and K showed relatively weak correlations, especially in capitula and living green segments (0-10 cm) of the plant (r = 0.50). The strongest correlations were revealed between 137 Cs and Rb (r = 0.89), and between 137 Cs and stable Cs (r = 0.84). This suggests similarities between 137 Cs and Rb in uptake and relocation within the Sphagnum, but that 137 Cs differs from K.

  14. The distribution of (137)Cs, K, Rb and Cs in plants in a Sphagnum-dominated peatland in eastern central Sweden.

    Science.gov (United States)

    Vinichuk, M; Johanson, K J; Rydin, H; Rosén, K

    2010-02-01

    We record the distribution of (137)Cs, K, Rb and Cs within individual Sphagnum plants (down to 20cm depth) as well as (137)Cs in vascular plants growing on a peatland in eastern central Sweden. In Calluna vulgaris(137)Cs was mainly located within the green parts, whereas Andromeda polifolia, Eriophorum vaginatum and Vaccinium oxycoccos showed higher (137)Cs activity in roots. Carex rostrata and Menyanthes trifoliata showed variable distribution of (137)Cs within the plants. The patterns of (137)Cs activity concentration distribution as well as K, Rb and Cs concentrations within individual Sphagnum plants were rather similar and were usually highest in the capitula and/or in the subapical segments and lowest in the lower dead segments, which suggests continuous relocation of those elements to the actively growing apical part. The (137)Cs and K showed relatively weak correlations, especially in capitula and living green segments (0-10cm) of the plant (r=0.50). The strongest correlations were revealed between (137)Cs and Rb (r=0.89), and between (137)Cs and stable Cs (r=0.84). This suggests similarities between (137)Cs and Rb in uptake and relocation within the Sphagnum, but that (137)Cs differs from K. Copyright 2009 Elsevier Ltd. All rights reserved.

  15. Uptake and distribution of 137Cs and stable Cs by microorganisms isolated from mushroom substrata in the Japanese forests

    International Nuclear Information System (INIS)

    Kuwahara, Chikako; Fukumoto, Atsushi; Kato, Fumio; Sugiyama, Hideo

    2004-01-01

    The pH values of wild mushroom substrata, the influence of pH in medium on the appearance frequencies of microorganisms from mushroom substrata, and growth and Cs uptake by several microorganisms were investigated. The results showed that the pH values of 42 mushroom substrata were slightly acidic. There was no remarkable difference in the appearance frequencies of filamentous actinomycetes and planktonic bacteria at pH 5, 6 and 7, except in the samples of mushroom substrata from Mt. Fuji. The values of Cs concentration ratio (CR) for microorganisms isolated from mushroom substrata and for mushrooms were almost the same level, suggesting that those microorganisms could take up Cs in substrata and reserve Cs in their cells. (author)

  16. Facile synthesis and characterization of CsPbBr3 and CsPb2Br5 ...

    Indian Academy of Sciences (India)

    2018-03-23

    Mar 23, 2018 ... All-inorganic caesium lead-halide perovskite CsPbBr3 and ... optoelectronic materials owing to their stabilities and highly efficient photoluminescence (PL). ... chemical tenability [2], hybrid organic–inorganic lead halide-.

  17. Energy- and temperature dependences of secondary electron emission of CsI- and CsBr layers doped with Cd

    International Nuclear Information System (INIS)

    Galij, P.V.; Tsal', N.A.

    1983-01-01

    The energy and temperature dependences of the secondary electron emission coefficient (SEEC) of CsI-Cd-, CsBr-Cd-, CsI-CsBr layers have been studied. The effect of bivalent cadmium impurity on the SEEC value is investigated. It is shown that implantation of small amounts of Cd 2+ impurity into the lattice of the initial monocrystals might increase the SEEC values of the layers. Temperature dependences (TD) of SEEC are measured and the possibility of comparing experimental results with the Dekker formula is analyzed. A conclusion is drawn that the Dekker model well describes the TD of SEEC of doped layers at temperatures T < or approximately 100 deg C. At elevated temperatures., along with secondary electron scattering on phonons, one should take into account their scattering on vacancies

  18. Seperation of CsCl from LiCl-CsCl molten salt by cold finger melt cryst allization

    Energy Technology Data Exchange (ETDEWEB)

    Versey, Joshua R. [Dept. of Chemical and Materials Engineering and Nuclear Engineering Program University of Idaho, Idaho (United States); Phongikaroon, Supathorn [Dept. of Mechanical and Nuclear Engineering Virginia Commonwealth University, Richmond (Korea, Republic of); Simpson, Michael F. [Dept. of Metallurgical Engineering University of Utah, Utah (Korea, Republic of)

    2014-06-15

    This study provides a fundamental understanding of a cold finger melt crystallization technique by exploring the heat and mass transfer processes of cold finger separation. A series of experiments were performed using a simplified LiCl-CsCl system by varying initial CsCl concentrations (1, 3, 5, and 7.5 wt%), cold finger cooling rates (7.4, 9.8, 12.3, and 14.9 L/min), and separation times (5, 10, 15, and 30 min). Results showed a potential recycling rate of 0.36 g/min with a purity of 0.33 wt% CsCl in LiCl. A CsCl concentrated drip formation was found to decrease crystal purity especially for smaller crystal formations. Dimensionless heat and mass transfer correlations showed that separation production is primarily influenced by convective transfer controlled by cooling gas flow rate, where correlations are more accurate for slower cooling gas flow rates.

  19. Physicochemical properties of the CsNO2-CsOH-H2O ternary system at 25 deg C

    International Nuclear Information System (INIS)

    Protsenko, P.I.; Medvedev, B.S.; Popova, T.B.

    1977-01-01

    Saturated solutions of the CsNO 2 - CsOH- H 2 O system have been studied at 25 deg C by the methods of solubility, viscosity, electric conductivity, refractometry and density. It is stated that no solid phase of a new composition is formed in the system. While adding hydroxide to the saturated solution of cesium nitride, a considerable salting-out of the latter takes place

  20. Immobilized nickel hexacyanoferrate on activated carbons for efficient attenuation of radio toxic Cs(I) from aqueous solutions

    International Nuclear Information System (INIS)

    Lalhmunsiama; Lalhriatpuia, C.; Tiwari, Diwakar; Lee, Seung-Mok

    2014-01-01

    Highlights: • Rice hulls and areca nut wastes are utilized to obtain activated carbons. • Nickel hexacyanoferrate is immobilized on activated carbon samples. • Materials are characterized by SEM–EDX and XRD data. • Materials are employed in attenuation of Cs(I) under batch and column studies. • Possible mechanism is deduced at solid/solution interface. - Abstract: The aim of this study is to immobilize nickel hexacyanoferrate onto the large surface of activated carbons (ACs) precursor to rice hulls and areca nut waste materials. These nickel hexacyanoferrate immobilized materials are then assessed in the effective attenuation of radio logically important cesium ions from aqueous solutions. The solid samples are characterized by the XRD analytical method and surface morphology is obtained from the SEM images. The batch reactor experiments show that an increase in sorptive pH (2.0–10.0) apparently not affecting the high percent uptake of Cs(I). Equilibrium modeling studies suggest that the data are reasonably and relatively fitted well to the Langmuir adsorption isotherm. Kinetic studies show that sorption process is fairly rapid and the kinetic data are fitted well to the pseudo-second order rate model. Increasing the background electrolyte concentration from 0.001 to 0.1 mol/L NaCl causes insignificant decrease in Cs(I) removal which infers the higher selectivity of these materials for Cs(I) from aqueous solutions. Further, the column reactor operations enable to obtain the breakthrough data which are then fitted to the Thomas non-linear equation as to obtain the loading capacity of column for Cs(I). The results show that the modified materials show potential applicability in the attenuation of radio toxic cesium from aqueous solution

  1. Determination and speciation of plutonium, americium, uranium, thorium, potassium and 137Cs in a Venice canal sediment sample

    International Nuclear Information System (INIS)

    Testa, C.; Desideri, D.; Guerra, F.; Meli, M.A.; Roselli, C.; Degetto, S.

    1998-01-01

    A sequential extraction method consisting of six operationally-defined fractions has been developed for determining the geochemical partitioning of natural (U, Th, 40 K) and anthropogenic (Pu, Am, 137 Cs) radionuclides in a 40-50 cm deep sediment sample collected in a Venice canal. Extraction chromatography was used for the chemical separation of a single radionuclide; the final recoveries were calculated by adding 232 U, 228 Th, 242 Pu and 243 Am as the yield tracers. After electrodeposition the alpha spectrometry was carried out. 137 Cs and 40 K were measured by gamma spectrometry. The total concentrations in the wet sample, obtained by a complete disgregation of the matrix by NaOH fusion, were the following: 239+240 Pu = 610 ± 80 mBq/kg, 238 Pu = 13 ± 5mBq/kg, 241 Am 200 ± 30 mBq/kg, 137 Cs = 6.9 ± 1.1 Bq/kg, U = 1.33 ± 0.14 ppm, Th = 2.69 ± 0.26 ppm, K = 0.72 ± 0.04 %. The mean ratio 238 Pu/ 239+240 Pu ( 0.02) shows a contamination due essentially to fall-out and U and Th alpha spectra indicate the natural origin of two elements. The absence of 134 Cs proves that the sediment was not affected by the Chernobyl fall-out. For the speciation, the following fractions were considered: water soluble, carbonates, Fe-Mn oxides, organic matter, acid soluble, residue. Pu (about 65%) and Am (about 90%) were present predominantly in the carbonate fraction; U was more distributed and about 30% appeared both in the carbonate fraction and in the residue; the majority of Th was present in the residue (about 67%); 40 K was totally present in the residue; and 137 Cs was found mostly in the acid soluble fraction (about 46%) and in the residue (about 40%)

  2. Thermal gravimetric analysis of the CsCuCl3, Cs2CuCl4 and Cs2CuCl4x2H2O crystals

    International Nuclear Information System (INIS)

    Soboleva, L.V.; Vasil'eva, M.G.

    1977-01-01

    The thermal characteristics of crystals of Cs 2 CuCl 4 , Cs 2 CuCl 4 x2H 2 O, and CsCuCl 3 were investigated thermogravimetrically. The derivatogram of the Cs 2 CuCl 4 crystal is characterized by the presence of a single endothermal effect at 505 deg C. The derivatogram of the Cs 2 CuCl 4 x2H 2 O crystal contains three endothermal effects: at 40, 135, and 480 deg C. The derivatogram of the CsCuCl 3 crystal shows the presence of two endothermal effects at 142 and 455 deg C. The thermogravimetric data on Cs 2 CuCl 4 and CsCuCl 3 crystals reveal crystal decomposition on melting; hence, these crystals cannot be grown from melts

  3. Evaluation of Cs-134 and Cs-137 in sugar by non-destructive analysis

    Energy Technology Data Exchange (ETDEWEB)

    Correira, Filipe Lopes de Barros; Santos Júnior, José Araújo dos; Amaral, Romilton dos Santos; Santos, Josineide Marques do Nascimento; Medeiros, Nilson Vicente da Silva; Santos Junior, Otávio Pereira dos, E-mail: filipelbck@gmail.com, E-mail: jaraujo@ufpe.br, E-mail: romilton@ufpe.br, E-mail: josineide.santos@ufpe.br, E-mail: nilson.medeiros@ufpe.br, E-mail: otavio.santos@vitoria.ifpe.edu.br [Universidade Federal de Pernambuco (RAE/UFPE), Recife, PE (Brazil). Departamento de Energia Nuclear. Grupo de Radioecologia; Vieira, José Wilson, E-mail: jose.wilson59@uol.com.br [Instituto Federal de Pernambuco (IFPE), Recife (Brazil); Valois, Rhaiana Caminha, E-mail: rhaianavalois@hotmail.com [Colégio Militar do Recife, PE (Brazil)

    2017-07-01

    The spread of anthropogenic radioisotopes in the environment comes from nuclear tests and accidents that occurred in the past, which justifies constant monitoring, to guarantee the safety and control of the activities that involve these applications. Brazil, when exporting some food products, depending on the country of origin, a radiometric report is required, especially for sugar that has high world consumption and the possibility of contamination of the population, when radioisotope is present. Therefore, the investigation of the levels of Cs-134 and Cs-137 in sugar matrices is necessary to predict radioecological emergency situations. The National Nuclear Energy Commission, the agency that oversees nuclear applications in Brazil, With Resolution No. 102 of December 22, 2010 approved regulatory positions, including levels of action for food control, recommended to restrict the marketing of food products in Brazil. General, whose specific activity is higher than the limit of 1.0 kBq / kg for the said isotopes of cesium independently. Aiming for improvements in the analyzes that are already performed in the Laboratory of Radioecology and Environmental Control of the Department of Nuclear Energy of the Federal University of Pernambuco to assurance the quality of sugar marketed in Brazil, a standard procedure for the analysis of these radionuclides in this matrix was determined. High resolution gamma spectrometry with non-destructive analysis was used to perform the tests. Priority was given to parameters that directly influence the qualitative and quantitative analysis of these radioactive elements, such as calibration in energy and efficiency, resolution, influence of self-absorption, counting statistics directly associated with the time of analysis, influence of background radiation and geometry analysis. (author)

  4. Evaluation of Cs-134 and Cs-137 in sugar by non-destructive analysis

    International Nuclear Information System (INIS)

    Correira, Filipe Lopes de Barros; Santos Júnior, José Araújo dos; Amaral, Romilton dos Santos; Santos, Josineide Marques do Nascimento; Medeiros, Nilson Vicente da Silva; Santos Junior, Otávio Pereira dos; Valois, Rhaiana Caminha

    2017-01-01

    The spread of anthropogenic radioisotopes in the environment comes from nuclear tests and accidents that occurred in the past, which justifies constant monitoring, to guarantee the safety and control of the activities that involve these applications. Brazil, when exporting some food products, depending on the country of origin, a radiometric report is required, especially for sugar that has high world consumption and the possibility of contamination of the population, when radioisotope is present. Therefore, the investigation of the levels of Cs-134 and Cs-137 in sugar matrices is necessary to predict radioecological emergency situations. The National Nuclear Energy Commission, the agency that oversees nuclear applications in Brazil, With Resolution No. 102 of December 22, 2010 approved regulatory positions, including levels of action for food control, recommended to restrict the marketing of food products in Brazil. General, whose specific activity is higher than the limit of 1.0 kBq / kg for the said isotopes of cesium independently. Aiming for improvements in the analyzes that are already performed in the Laboratory of Radioecology and Environmental Control of the Department of Nuclear Energy of the Federal University of Pernambuco to assurance the quality of sugar marketed in Brazil, a standard procedure for the analysis of these radionuclides in this matrix was determined. High resolution gamma spectrometry with non-destructive analysis was used to perform the tests. Priority was given to parameters that directly influence the qualitative and quantitative analysis of these radioactive elements, such as calibration in energy and efficiency, resolution, influence of self-absorption, counting statistics directly associated with the time of analysis, influence of background radiation and geometry analysis. (author)

  5. Speciation of Cs-137 in fertilizers amended soils

    International Nuclear Information System (INIS)

    Mocanu, N.; Breban, D.C.

    1999-01-01

    One of the most used agricultural countermeasures to reduce the uptake of radionuclides from soil into plants is the chemical treatment of the soil with fertilizers. The distribution of a radionuclide between different physico chemical forms is essential to characterize its behaviour and the biological impact on the environment. To assess a radionuclide bioavailability to the soil-plant transfer, the chemical forms that are most relevant are the water soluble and exchangeable ones. Laboratory experiments were conducted to determine the potential modifications in time of the Cs-137 distribution in the two soil fractions, induced by the treatment with different K-based fertilizers. The two types of soil were selected taking into account their importance for the agricultural use in Romania. By the sequential extraction method the distribution of 137 Cs has been determined in the water soluble and exchangeable fractions separated from the soils after 1 day, 1 week, 1 month and 4 months, respectively. For the reference untreated soils, experimental data revealed that less than 1 percent of Cs-137 is associated to the water soluble fraction for both types of soil. Around 4 percents of the total amount of Cs-137 in the brown-reddish soil and 13 percents in the alluvial one were associated to the exchangeable fraction. The differences between the Cs-137 distribution are correlated to the higher content of dust and clay in the brown reddish soil, which are strong binders for Cs ions. The application of the two fertilizers releasing fast the K ions (KCl and potassium salt), determined from at the first moment after the contamination a reduction of the Cs-137 concentration in both fraction. The effect was most pronounced for the soluble fraction in the brown -reddish soil: with a factor of 8 in case of KCl treatment and 5 in case of potassium salt. For the others experimental cases the concentration of Cs-137 in both fractions was slightly reduced, with factors between (1

  6. Bioaccumulation of 137Cs by microorganisms isolated from soils contaminated with radionuclides

    International Nuclear Information System (INIS)

    Pipiska, M.; Hornik, M.; Augustin, J.

    2003-01-01

    With the aim to evaluate the possibility of utilisation of autochtone population of soil organisms, alone or with participation of higher plants, in the processes of bioremediation the authors quantitatively determined a number of psychrophyllic and mezophyllic germs in the soils contaminated by low-level activities of Cs-137 (0.08 - 2.8 kBq/g). Hereafter they gained isolates of clean cultures of mushrooms and actinomycetes and they determined their bioacumulative activity of Cs-137 at growing conditions. The authors found out, that a number of reproductionable psychrophyllic and mezophyllic germs are significantly lower in the soils with the highest contamination by radionuclides than in the soils with low contamination. They gained the clean cultures of 5 isolates of micromycetes and 3 isolates of actinomycetes from contaminated soil. The micromycetes demonstrated the highest values of bioaccumulation of caesium 39 nmol/g of wet biomass at the growing conditions. In actionoomycetes these values were 4.7 nmol/g (approximately in one order lower). The significant part of cesium accumulated by cell matter at growing conditions were localised in cell matter and it could not be removed by washing with 0.9 percent of NaCl solution. The determined values of bioconcentration factor BCF recalculated on dry weight of biomass were in the range from 16.04 to 26.20 in micromycetes and 3.24 in actinomycetes. From this situation arise, that autochtone population of soil micromycetes and actionomycetes, which is found in contaminated soil, can relevantly participate in the processes of binding of biologically accessible forms of Cs-137 after a creation of suitable conditions for grow. (author)

  7. The adsorption of Cs+, Sr2+ and Ni2+ on bitumen: a mechanistic model

    International Nuclear Information System (INIS)

    Loon, L.R. Van; Kopajtic, Z.

    1991-01-01

    The adsorption of radionuclides on the waste matrix is a positive effect and contributes to the retardation of released radionuclides migrating to the geo-and biosphere. For the safety assessment studies, it is important to know whether or not radionuclides do adsorb on the waste matrix. In the present work the adsorption of 134 Cs + , 85 Sr 2+ and 63 Ni 2+ on bitumen was studied as a function of the pH and ionic strength of the equilibrium solution. Bitumen emulsions with well defined surfaces were used. The surface of bitumen is negatively charged due to the deprotonation of weak acid carboxyl groups at the interface. The functional group density amounts to 1.37.10 18 groups/m 2 and their deprotonation behaviour can be well described by the 'Ionizable Surface Group' model. Cs + , Sr 2+ and Ni 2+ adsorb on the surface by three different processes, i.e. ion exchange, outer sphere complexation and inner sphere surface complexation respectively. The adsorption depends on the pH and the ionic strength of the contact solution. Under near field conditions, Cs + and Sr 2+ do not adsorb on the bitumen due to the competition with Na + , K + and Ca 2+ present in the cement pore water in contact with the bitumen. Ni 2+ adsorption can also be neglected because the formation of neutral and anionic hydroxo complexes in solution competes strongly with the adsorption reaction. Other hydrolysable radionuclides of interest are expected to behave similarly to Ni 2+ . The main conclusion of the study is that the adsorption of radionuclides under near field conditions is expected to be very low. Consequently, this process need not to be considered in safety assessment studies. (author) figs., tabs., 30 refs

  8. An optical microscopy study of the swelling of wet-spun films of CsDNA as a function of hydration and CsCl concentration

    Science.gov (United States)

    Schwenker, Megan; Marlowe, Robert; Lee, Scott; Rupprecht, Allan

    2005-03-01

    Highly oriented, wet-spun films of DNA expand in the direction perpendicular to the helical axis as the hydration of the film is increased. CsDNA films with a high CsCl content show an unexpected shrinkage at a relative humidity of 92%. Our most recent experiments have been to measure the perpendicular dimension of CsDNA as a function of both hydration and concentration of CsCl. Our preliminary results show that no shrinkage is observed at low contents of CsCl, showing that the CsCl plays an integral role in the shrinkage phenomenon.

  9. Correlations between potassium, rubidium and cesium ({sup 133}Cs and {sup 137}Cs) in sporocarps of Suillus variegatus in a Swedish boreal forest

    Energy Technology Data Exchange (ETDEWEB)

    Vinichuk, M., E-mail: Mykhailo.Vinichuk@slu.s [Department of Soil and Environment, Swedish University of Agricultural Sciences, P.O. Box 7014, SE-750 07 Uppsala (Sweden); Department of Ecology, Zhytomyr State Technological University, 103 Cherniakhovsky Str., 10005 Zhytomyr (Ukraine); Rosen, K.; Johanson, K.J. [Department of Soil and Environment, Swedish University of Agricultural Sciences, P.O. Box 7014, SE-750 07 Uppsala (Sweden); Dahlberg, A. [Department of Forest Mycology and Pathology, Swedish University of Agricultural Sciences, P.O. Box 7026, 750 07 Uppsala (Sweden)

    2011-04-15

    An analysis of sporocarps of ectomycorrhizal fungi Suillus variegatus assessed whether cesium ({sup 133}Cs and {sup 137}Cs) uptake was correlated with potassium (K) or rubidium (Rb) uptake. The question was whether intraspecific correlations of Rb, K and {sup 133}Cs mass concentrations with {sup 137}Cs activity concentrations in sporocarps were higher within, rather than among, different fungal species, and if genotypic origin of sporocarps within a population affected uptake and correlation. Sporocarps (n = 51) from a Swedish forest population affected by the fallout after the Chernobyl accident were studied. The concentrations were 31.9 {+-} 6.79 g kg{sup -1} for K (mean {+-} SD, dwt), 0.40 {+-} 0.09 g kg{sup -1} for Rb, 8.7 {+-} 4.36 mg kg{sup -1} for {sup 133}Cs and 63.7 {+-} 24.2 kBq kg{sup -1} for {sup 137}Cs. The mass concentrations of {sup 133}Cs correlated with {sup 137}Cs activity concentrations (r = 0.61). There was correlation between both {sup 133}Cs concentrations (r = 0.75) and {sup 137}Cs activity concentrations (r = 0.44) and Rb, but the {sup 137}Cs/{sup 133}Cs isotopic ratio negatively correlated with Rb concentration. Concentrations of K and Rb were weakly correlated (r = 0.51). The {sup 133}Cs mass concentrations, {sup 137}Cs activity concentrations and {sup 137}Cs/{sup 133}Cs isotopic ratios did not correlate with K concentrations. No differences between, within or, among genotypes in S. variegatus were found. This suggested the relationships between K, Rb, {sup 133}Cs and {sup 137}Cs in sporocarps of S. variegatus is similar to other fungal species. - Highlights: {yields} We studied uptake of Cs ({sup 133}Cs and {sup 137}Cs), K and Rb by Suillus variegates sporocarps. {yields} Genotypic origin of fungus did not affect uptake of studied elements (isotopes). {yields} Genotypic origin did not affect correlation between Cs ({sup 133}Cs and {sup 137}Cs), K and Rb.

  10. CsMYB5a and CsMYB5e from Camellia sinensis differentially regulate anthocyanin and proanthocyanidin biosynthesis.

    Science.gov (United States)

    Jiang, Xiaolan; Huang, Keyi; Zheng, Guangshun; Hou, Hua; Wang, Peiqiang; Jiang, Han; Zhao, Xuecheng; Li, Mingzhuo; Zhang, Shuxiang; Liu, Yajun; Gao, Liping; Zhao, Lei; Xia, Tao

    2018-05-01

    Tea is one of the most widely consumed nonalcoholic beverages worldwide. Polyphenols are nutritional compounds present in the leaves of tea plants. Although numerous genes are functionally characterized to encode enzymes that catalyze the formation of diverse polyphenolic metabolites, transcriptional regulation of those different pathways such as late steps of the proanthcoyanidin (PA) pathway remains unclear. In this study, using different tea transcriptome databases, we screened at least 140 R2R3-MYB transcription factors (TFs) and grouped them according to the basic function domains of the R2R3 MYB TF superfamily. Among 140 R2R3 TFs, CsMYB5a and CsMYB5e were chosen for analysis because they may be involved in PA biosynthesis regulation. CsMYB5a-overexpressing tobacco plants exhibited downregulated anthocyanin accumulation but a high polymeric PA content in the flowers. Overexpression of CsMYB5e in tobacco plants did not change the anthocyanin content but increased the dimethylaminocinnamaldehyde-stained PA content. RNA-seq and qRT-PCR analyses revealed that genes related to PA and anthocyanin biosynthesis pathways were markedly upregulated in both CsMYB5a- and CsMYB5e-overexpressing flowers. Three UGTs and four GSTs were identified as involved in PA and anthocyanin glycosylation and transportation in transgenic plants. These results provide new insights into the regulation of PA and anthocyanin biosynthesis in Camellia sinensis. Copyright © 2018 Elsevier B.V. All rights reserved.

  11. Analysis on the influence of forest soil characteristics on radioactive Cs infiltration and evaluation of residual radioactive Cs on surfaces.

    Science.gov (United States)

    Mori, Yoshitomo; Yoneda, Minoru; Shimada, Yoko; Fukutani, Satoshi; Ikegami, Maiko; Shimomura, Ryohei

    2018-03-29

    We investigated the depth profiles of radioactive Cs, ignition loss, and cation exchange capacity (CEC) in five types of forest soils sampled using scraper plates. We then simulated the monitored depth profiles in a compartment model, taking ignition loss as a parameter based on experimental results showing a positive correlation between ignition loss and the CEC. The calculated values were comparable with the monitored values, though some discrepancy was observed in the middle of the soil layer. Based on decontamination data on the surface dose rate and surface contamination concentration, we newly defined a surface residual index (SRI) to evaluate the residual radioactive Cs on surfaces. The SRI value tended to gradually decrease in forests and unpaved roads and was much smaller in forests and on unpaved roads than on paved roads. The radioactive Cs was assumed to have already infiltrated underground 18 months after the nuclear power plant accident, and the sinking was assumed to be ongoing. The SRI values measured on paved roads suggested that radioactive Cs remained on the surfaces, though a gradual infiltration was observed towards the end of the monitoring term. The SRI value is thought to be effective in grasping the rough condition of residual radioactive Cs quickly at sites of decontamination activity in the field. The SRI value may be serviceable for actual contamination works after further research is done to elucidate points such as the relation between the SRI and the infiltration of radioactive Cs in various types of objects.

  12. Elucidation and functional characterization of CsPSY and CsUGT promoters in Crocus sativus L.

    Science.gov (United States)

    Bhat, Archana; Mishra, Sonal; Kaul, Sanjana; Dhar, Manoj K

    2018-01-01

    The dried stigmas of Crocus sativus constitute the saffron, which is considered to be the costliest spice of the world. Saffron is valuable for its constituents, which are mainly apocarotenoids. In order to enhance the production of apocarotenoids, it is imperative to understand the regulation of apocarotenoid biosynthetic pathway. In C. sativus, although the pathway has been elucidated, the information regarding the regulation of the pathwaygenes is scanty. During the present investigation, the characterization of promoters regulating the expression of two important genes i.e. CsPSY and CsUGT was performed. We successfully cloned the promoters of both the genes, which were functionally characterized in Crocus sativus and Nicotiana tabaccum. In silico analysis of the promoters demonstrated the presence of several important cis regulatory elements responding tolight, hormonesand interaction with transcription factors (TFs). Further analysis suggested the regulation of CsPSY promoter by Abscisic acid (ABA) and that of CsUGT by Gibberellic acid (GA). In addition, we also observed ABA and GA mediated modulation in the expression of significant TFs and CsPSY and CsUGT transcripts. Overall, the study addresses issues related to regulation of key genes of apocarotenoid pathway in C.sativus.

  13. Luminescence properties of undoped CsCaCl3 and CsSrCl3 crystalline scintillators

    International Nuclear Information System (INIS)

    Fujimoto, Yutaka; Saeki, Keiichiro; Koshimizu, Masanori; Asai, Keisuke; Yanagida, Takayuki

    2015-01-01

    Intrinsic luminescence properties of undoped CsCaCl 3 and CsSrCl 3 crystalline scintillators were studied. The crystal samples were grown by a vertical Bridgman method. Photoluminescence spectra of the crystals showed Auger-free luminescence (AFL) at 310 nm and self-trapped emission (STE) at 400 nm for CsCaCl 3 and 465 nm for CsSrCl 3 , when vacuum ultraviolet (VUV) light at 84 nm and 160 nm excited the crystals. X-ray excited radioluminescence spectra of the crystals showed some emission bands in the 280-600 nm wavelength range, which are owing to AFL, STE, and other origins such as lattice defects and impurities. Scintillation light yield was 400-300 ph/MeV, and the principal scintillation decay time about 2.5 ns and 12 ns for CsCaCl 3 and 1.8 ns and 13 ns for CsSrCl 3 . (author)

  14. Temporal changes and factors influencing {sup 137}Cs concentration in vegetation colonizing an exposed lake bed over a three-year period

    Energy Technology Data Exchange (ETDEWEB)

    Hinton, T.G.; Bell, C.M. [Savannah River Ecology Laboratory, The University of Georgia, Aiken, SC (United States); Whicker, F.W. [Colorado State University, Fort Collins, CO (United States); Philippi, T. [Savannah River Ecology Laboratory, The University of Georgia, Aiken, SC (United States)

    1999-05-01

    Activity concentrations of {sup 137}Cs in sediments, as well as extractable sediment concentrations of K, Na, Mg, Ca, Mn, Zn and P, pH, percent organic matter and cation exchange capacity, were used as independent variables in an incomplete principal component analysis to identify factors affecting {sup 137}Cs activity concentrations in 12 species of native wetland and terrestrial plants invading a recently exposed lake bed. Sediments in the lake had been contaminated 35 years previously from discharges at a nuclear production reactor. {sup 137}Cs activity concentrations in plants were positively correlated with sediment concentrations of Na and {sup 137}Cs, and inversely correlated to K and pH. Significant decreases in concentrations of sediment constituents (from 3 to 77%), as well as a 42% decline in {sup 137}Cs activity concentrations in plants, occurred during the three-year period. Significant differences in {sup 137}Cs activity concentrations among plant species, driven by low concentrations in cattails (Typha latifolia), were observed. Terrestrial species had significantly lower activity concentrations of {sup 137}Cs than species classified as wetland (arithmetic mean{+-}S.E. of 1069{+-}151 and 2602{+-}394, respectively). Concentration ratios (Bq kg{sup -1} dry plant/Bq kg{sup -1} dry soil) were among the highest reported in the literature (arithmetic mean{+-}S.D.=12.5{+-}28.9; geometric mean=1.6, geometric S.D.=1.4) and were attributed to kaolinitic sediments of pH<5, organic matter <5%, K concentrations <15 ppm and cation exchange capacity <5 meq (100 g{sup -1}). Even though {sup 137}Cs was released into the system over 35 years ago, lowering of the water caused {sup 137}Cs in the newly formed terrestrial system to behave like a fresh, rather than aged, deposit (initial uptake rates by plants were high and subsequent reductions in bioavailability were rapid). Implications for management of contaminated reservoirs from a public risk perspective are

  15. Redetermination of the cubic struvite analogue Cs[Mg(OH26](AsO4

    Directory of Open Access Journals (Sweden)

    Matthias Weil

    2009-01-01

    Full Text Available In contrast to the previous refinement from photographic data [Ferrari et al. (1955. Gazz. Chim. Ital. 84, 169–174], the present redetermination of the title compound, caesium hexaaquamagnesium arsenate(V, revealed the Cs atom to be on Wyckoff position 4d instead of Wyckoff position 4b of space group Foverline{4}3m. The structure can be derived from the halite structure. The centres of the complex [Mg(OH26] octahedra and the AsO4 tetrahedra (both with overline{4}3m symmetry are on the respective Na and Cl positions. The building units are connected to each other by O—H...O hydrogen bonds. The Cs+ cations (overline{4}3m symmetry are located in the voids of this arrangement and exhibit a regular cuboctahedral 12-coordination to the O atoms of the water molecules. The O atom bonded to As has 2mm site symmetry (Wyckoff position 24f and the water-molecule O atom has m site symmetry (Wyckoff position 48h.

  16. O lirismo em György Lukács

    Directory of Open Access Journals (Sweden)

    Arlenice Almeida da Silva

    2009-06-01

    Full Text Available O artigo visa a examinar o tratamento dado ao lírico na obra estética do jovem Lukács. Em A alma e as formas o autor examina a poesia de Stefan George, encontrando nela elementos formais que apontam para o surgimento de um novo lirismo. Tal "forma significativa" possibilita ao autor introduzir uma abordagem do conceito de modernidade, em viés crítico e fenomenológico. Empreendimento que será completado em A teoria do romance, quando a tendência lírica se apresentará exacerbada, contaminando e alterando as configurações dos demais gêneros.The paper aims to examine the treatment of lyrical in the aesthetics work of the young Lukács. In The Soul and the Forms the author examines the poetry of Stefan George, finding on it formal elements that point out to the emergence of a new lyricism. This "significant form" allows the author to introduce an approach of the concept of modernity, in critical and phenomenological bias. Work that will be completed in The theory of Love, when the lyric trend will be exacerbated, contaminating and altering the settings of the other genera.

  17. Uptake and transfer factors of 137Cs by mushrooms

    International Nuclear Information System (INIS)

    Heinrich, G.

    1991-01-01

    The 137 Cs content of 118 species (668 samples) of higher fungi collected in the period from August 1984 to October 1989 at three different locations in Styria, Austria, was determined by gamma-spectrometry. The Cs-content of most mushrooms has been increasing since September 1986. In order to find out which factors determine the 137 Cs-contamination of mushrooms and the transfer-value soil to mushroom, the concentration of total and plant-available radiocesium in soils as well as the pH-value, the content of humus, clay, silt, sand, exchangeable cations, the composition of the clay minerals, and the particle size distribution of the soils of two different locations were examined. The higher the 137 Cs contamination of the soil, the thicker the layer of humus and the higher the content of humus, the lower the pH-value, and the lower the amount of essential cations, especially of K + , the higher the amount of 137 Cs plant-available will be. Therefore, the contamination of the mushrooms in the coniferous forest of Koralpenblick (1000 m) is higher than in the mixed forest at the Rosenberg around Graz at approx. 500 m height. Of 26 different species of mushrooms measured at both sites, only 61% show the highest TF-values soil to mushrooms also at the Koralpenblick. In the spruce forest at Koralpenblick there are many species of mushrooms with high 137 Cs-contamination which were not found at the Rosenberg. However, the properties of the species to which a mushroom belongs are more important than environmental conditions and soil properties. The transfer values of 40 K stay within narrow bounds, whereas those of 137 Cs differ widely. (orig.)

  18. Accurate absolute measurement of trapped Cs atoms in a MOT

    International Nuclear Information System (INIS)

    Talavera O, M.; Lopez R, M.; Carlos L, E. de; Jimenez S, S.

    2007-01-01

    A Cs-133 Magneto-Optical Trap (MOT) has been developed at the Time and Frequency Division of the Centro Nacional de Metrologia, CENAM, in Mexico. This MOT is part of a primary frequency standard based on ultra-cold Cs atoms, called CsF-1 clock, under development at CENAM. In this Cs MOT, we use the standard configuration (σ + - σ - ) 4-horizontal 2-vertical laser beams 1.9 cm in diameter, with 5 mW each. We use a 852 nm, 5 mW, DBR laser as a master laser which is stabilized by saturation spectroscopy. Emission linewidth of the master laser is l MHz. In order to amplify the light of the master laser, a 50 mW, 852 nm AlGaAs laser is used as slave laser. This slave laser is stabilized by light injection technique. A 12 MHz red shift of the light is performed by two double passes through two Acusto-Optic Modulators (AOMs). The optical part of the CENAMs MOT is very robust against mechanical vibration, acoustic noise and temperature changes in our laboratory, because none of our diode lasers use an extended cavity to reduce the linewidth. In this paper, we report results of our MOT characterization as a function of several operation parameters such as the intensity of laser beams, the laser beam diameter, the red shift of light, and the gradient of the magnetic field. We also report accurate absolute measurement of the number of Cs atoms trapped in our Cs MOT. We found up to 6 x 10 7 Cs atoms trapped in our MOT measured with an uncertainty no greater than 6.4%. (Author)

  19. Photoluminescence and radiation response properties of Ce3+-doped CsCaCl3 crystalline scintillator

    International Nuclear Information System (INIS)

    Fujimoto, Yutaka; Saeki, Keiichiro; Tanaka, Hironori; Yahaba, Takuma; Koshimizu, Masanori; Asai, Keisuke; Yanagida, Takayuki

    2016-01-01

    In this paper, we report on the photoluminescence and scintillation properties of a newly developed CsCaCl 3 :Ce (0.5 mol%) crystalline scintillator grown by the vertical Bridgman method. The fluorescence quantum efficiency for the Ce 3+ characteristic emission bands centered at around 350–400 nm was 76% under excitation at 330 nm light. The photoluminescence decay time of the Ce 3+ was approximately 32 ns. When x-ray excited the crystal, intense emission bands were observed at 350–400 nm, and could be attributed to the Ce 3+ emission. The scintillation light yield of the developed crystal was ∼7600 ph MeV −1 compared to a NaI:Tl commercial scintillator, and the principal scintillation decay time was approximately 340 ns plus two fast components of around 1.6 ns and 45 ns. (paper)

  20. Radiogenotoxicological effect of signal nuclide 134Cs on somatic and germ cells

    Institute of Scientific and Technical Information of China (English)

    ZhuShou-Peng; XiaFen; 等

    1997-01-01

    Chromosome at aberation rates in bone marrow cells and micronucleus formation in bone marrow polychromatic erythrocytes both rise with increase in radioactivities of 134Cs,and can be fitted to power functions of radioactivities of 134Cs.In spermatogonia 134Cs mainly induced chromatid breakage,and abnormalities in sperm can also be experessed as power functions of radioactivities of 134 Cs.

  1. Repression of CC16 by cigarette smoke (CS exposure.

    Directory of Open Access Journals (Sweden)

    Lingxiang Zhu

    Full Text Available Club (Clara Cell Secretory Protein (CCSP, or CC16 is produced mainly by non-ciliated airway epithelial cells including bronchiolar club cells and the change of its expression has been shown to associate with the progress and severity of Chronic Obstructive Pulmonary Disease (COPD. In an animal model, the lack of CC16 renders the animal susceptible to the tumorigenic effect of a major CS carcinogen. A recent population-based Tucson Epidemiological Study of Airway Obstructive Diseases (TESAOD has indicated that the low serum CC16 concentration is closely linked with the smoke-related mortality, particularly that driven by the lung cancer. However, the study of CC16 expression in well-defined smoke exposure models has been lacking, and there is no experimental support for the potential causal link between CC16 and CS-induced pathophysiological changes in the lung. In the present study, we have found that airway CC16 expression was significantly repressed in COPD patients, in monkey CS exposure model, and in CS-induced mouse model of COPD. Additionally, the lack of CC16 exacerbated airway inflammation and alveolar loss in the mouse model. Therefore, CC16 may play an important protective role in CS-related diseases.

  2. 137 Cs as a tracer of the Catalan current

    International Nuclear Information System (INIS)

    Sanchez-Cabeza, J.A.; Molero, J.; Merino, J.; Pujol, L.; Mitchell, P.I.

    1995-01-01

    A number of nuclear power installations located in the north-western Mediterranean (NWM) area are known to enhance 137 Cs levels in various marine compartments. The nuclear fuel reprocessing plant at Marcoule (France) has been reported to originate a significant increase of 137 Cs in Rhone river waters and sediments because of the discharge of low-level liquid radioactive waste. This radionuclide may be used as a tracer of oceanographic processes in the NWM; in fact, 137 Cs of Rhone river origin has been detected in the Gulf of Lions by several authors. The results reported in this work correspond to various transect experiments in waters of the Catalan Sea and show that: (i) surface salinity measurements confirmed the presence of the Catalan current in the Cap de Creus area; (ii) the 1991 Cap de Creus transect showed clearly the presence of 137 Cs above a baseline level of 4.3 ± 0.2 Bq.m -3 ; (iii) the Cap de Salou transect showed elevated levels towards the coast; (iv) the 1992 Cap de Creus transect showed no structure at all. Therefore, it was concluded that traces of 137 Cs from the Marcoule nuclear fuel reprocessing plant were transported by the Catalan current and were detectable in the Catalan Sea with a complex spatio-temporal structure. (authors). 25 refs., 4 figs

  3. Cs-137 concentrations in the muscles of Walleye Pollack

    International Nuclear Information System (INIS)

    Morita, T.; Yoshida, K.

    2003-01-01

    High concentrations of Cs-137 were detected in the muscles of Walleye Pollack (Theragra chalcogramm) collected from Kitamiyamato banks (sampling on 25 Jul. 2000), Kamui area (16 Oct. 2000) and Niigata coasts (31 Jan. 2001). The concentrations were 0.35 ± 0.01, 0.41 ± 0.01, and 0.63 ± 0.02 Bq/kg-wet, respectively. The average concentration in our past investigations was about 0.25 ± 0.01 Bq/kg-wet. Samples from other areas, the coat of Kushiro (8 May 2001), North Tishima (13 Nov. 2000) and the Sea of Okhotsk (6 May 2001), had the average concentrations. There were no such high concentrations of Cs-137 in other fish species collected from Kitamiyamato banks, Kamui area, and Niigata coasts. Fish samples with high concentrations all make the migration in the north of Japan sea. These results would indicated that samples took in Cs-137 elements from sea-water or foods on the migration route. Cs-137 concentrations in muscles of walleye pollack does not increase with the body lengths unlike other marine fishes, which enables the comparison of Cs-137 concentrations between areas without considering the body lengths. Walleye Pollac migrates in the large area in the sea of Japan and draws near other country except Japan. These habits make Walleye Pollac the excellent bio indicators to monitor oceanic radioactive pollution

  4. Theoretical investigation of the Cs*Hen>=3 exciplexes

    International Nuclear Information System (INIS)

    Zbiri, Mohamed; Daul, Claude

    2005-01-01

    The X 2 Σ 1/2 , A 2 Π 1/2 , B 2 Σ 1/2 , and A 2 Π 3/2 states of Cs*He n exciplexes, with n={3,...,9}, are studied using first principle density functional theory (DFT) formalism combined with the zeroth order regular approximation (ZORA). The zero points energies (ZPEs) E 0 for Cs*He n are calculated at a first step, in order to estimate the stability of the studied exciplexes. Relativistic calculations are carried out including spin-orbit effect (SO), and potential energy surfaces of Cs*He 6 are shown. The electronic distribution shapes of the studied molecules are also discussed, and their emission lines are evaluated and compared to a new discovered experimental emission spectra, which has been recently assigned, using a semi-empirical model, to Cs(AΠ 1/2 )He 7 . Our first principle calculation suggests that the discovered emission line is most probably due to a decay of Cs(AΠ 1/2 )He 6

  5. Plant remediation of soil contaminated with 137Cs

    International Nuclear Information System (INIS)

    Yang Juncheng; Zhang Jianfeng; Zhu Yongyi; Chen Jingjie; Mei Yong; Jiang Huimin

    2005-01-01

    A pot experiment was conducted to evaluate the bio-remediation of soils contaminated with 137 Cs. The selected plants are Cucurbita moschata Duchesne, Brassica chinensis L, Chloris virgata, Beta oulgaris L. Hongye, Beta oulgaris L. Dongshengye and Beta oulgaris L. The soils samples were taken from the paddy field, 2 km from the Dayawan nuclear power plant and Qinshan nuclear power plant, respectively, and cinnamon soil from the cultivated land in Beijing. The results show that all the employed species of plant have a higher accumulation to 137 Cs with the increased grade of the radioactivity of 137 Cs. A good correlation exist with the coefficient (r 2 ) of 0.9989. When the contaminated radioactivity of 137 Cs is in the same level the uptake of Cucurbita moschata Duchesne, Brassica chinensis L. and Chloris virgata increased with the decrease of pH value ranged 5.22-7.69. The ability of bioremediation in the orders were Chloris virgata, Brassica chinensis L., Beta oulgaris L. Hongye, Cucurbita moschata Duchesne, Beta oulgaris L. and Beta oulgaris L. Dongshengye, according to the comprehensive evaluation of transfer factor, specific activity of plant in dry weight of biomass and total absorption of 137 Cs by the individual plant in the same area. (authors)

  6. Photoelectron Emission Studies in CsBr at 257 nm

    International Nuclear Information System (INIS)

    Maldonado, Juan R.; Liu, Zhi; Sun, Yun; Pianetta, Piero A.; Pease, Fabian W.

    2006-01-01

    CsBr/Cr photocathodes were found [1,2] to meet the requirements of a multi-electron beam lithography system operating with a light energy of 4.8 eV (257nm). The fact that photoemission was observed with a light energy below the reported 7.3 eV band gap for CsBr was not understood. This paper presents experimental results on the presence of intra-band gap absorption sites (IBAS) in CsBr thin film photo electron emitters, and presents a model based on IBAS to explain the observed photoelectron emission behavior at energies below band gap. A fluorescence band centered at 330 nm with a FWHM of about 0.34 eV was observed in CsBr/Cr samples under 257 nm laser illumination which can be attributed to IBAS and agrees well with previously obtained synchrotron photoelectron spectra[1] from the valence band of CsBr films

  7. Energy transfer mechanism in CsI:Eu crystal

    International Nuclear Information System (INIS)

    Yakovlev, V.; Trefilova, L.; Karnaukhova, A.; Ovcharenko, N.

    2014-01-01

    This paper studies the scintillation process in CsI:Eu crystal exposed to the pulse electron irradiation (E=0.25 MeV, t 1/2 =15 ns and W=0.003 J/cm 2 ). It has been proved that the energy transfer from the lattice to Eu 2+ ions in CsI:Eu occurs through the re-absorption of STE emission. The proposed model rests on the following experimental facts: (1) the activator emission at 2.68 eV rises gradually after the decay of the excitation pulse even at temperature lower than 90 K when V k centers are immobile; (2) the rise time of 2.68 eV emission and the decay time of STE emission have the same temperature dependences at T=78–300 K; (3) the excitation spectrum of 2.68 eV emission overlaps the emission spectrum of STE. -- Highlights: • The scintillation process in CsI:Eu was studied under pulsed electron irradiation. • A model of the energy transfer from the lattice to Eu 2+ ions in CsI:Eu was proposed. • Eu 2+ ions in CsI:Eu reabsorb the π-emission of self-trapped excitons

  8. Calculation of parameters of the interaction potential between excited alkali atoms and mercury atoms: The Cs*, Pr*-Hg interaction

    International Nuclear Information System (INIS)

    Glushkov, A.V.

    1994-01-01

    Based on the method of effective potential involving the new polarization interaction potential calculated from polarization diagrams of the perturbation theory in the Thomas-Fermi approximation, the main parameters of the interatomic potentials (equilibrium distances, potential well depth) are evaluated for a system consisting of an alkali atom in the ground and excited states and of a mercury atom. The results of calculations of quasi-molecular terms for the A-Hg system, where A = Na, Cs, Fr, are reported, some of which are obtained for the first time. A comparison is made with available experimental and theoretical data. 29 refs., 2 figs., 1 tab

  9. Knudsen cell--mass spectrometer studies of cesium--urania interactions. [Cs/sub 2/CO/sub 3/ or CsOH

    Energy Technology Data Exchange (ETDEWEB)

    Collins, J.L.; Osborne, M.F.; Malinauskas, A.P.; Lorenz, R.A.; Manning, S.R.

    1976-06-01

    Limited Knudsen cell--mass spectrometer studies were made of the partial pressures of cesium-containing species (assumed to be primarily Cs(g)) over Cs/sub 2/CO/sub 3/ and over phase equilibria involving UO/sub 2/ and probable Cs-U-O compounds formed from mixtures that initially contained either Cs/sub 2/CO/sub 3/-UO/sub 2/ or CsOH-UO/sub 2/. Although additional work is required to further define the equilibria involved, the data demonstrate unambiguously a significant reduction in cesium partial pressures due to probable Cs-U-O compound formation and indicate essentially identical behavior with either CsOH or Cs/sub 2/CO/sub 3/ as the starting material with UO/sub 2/.

  10. Imbedded Nanocrystals of CsPbBr3 in Cs4 PbBr6 : Kinetics, Enhanced Oscillator Strength, and Application in Light-Emitting Diodes.

    Science.gov (United States)

    Xu, Junwei; Huang, Wenxiao; Li, Peiyun; Onken, Drew R; Dun, Chaochao; Guo, Yang; Ucer, Kamil B; Lu, Chang; Wang, Hongzhi; Geyer, Scott M; Williams, Richard T; Carroll, David L

    2017-11-01

    Solution-grown films of CsPbBr 3 nanocrystals imbedded in Cs 4 PbBr 6 are incorporated as the recombination layer in light-emitting diode (LED) structures. The kinetics at high carrier density of pure (extended) CsPbBr 3 and the nanoinclusion composite are measured and analyzed, indicating second-order kinetics in extended and mainly first-order kinetics in the confined CsPbBr 3 , respectively. Analysis of absorption strength of this all-perovskite, all-inorganic imbedded nanocrystal composite relative to pure CsPbBr 3 indicates enhanced oscillator strength consistent with earlier published attribution of the sub-nanosecond exciton radiative lifetime in nanoprecipitates of CsPbBr 3 in melt-grown CsBr host crystals and CsPbBr 3 evaporated films. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  11. Potential of monitoring nuclides with the epiphyte Tillandsia usneoides: Uptake and localization of 133Cs.

    Science.gov (United States)

    Li, Peng; Zheng, Guiling; Chen, Xuan; Pemberton, Robert

    2012-12-01

    Epiphytic Tillandsia plants are efficient air pollution biomonitors and traditionally used to monitor atmospheric heavy metal pollution, but rarely nuclides monitoring. Here we evaluated the potential of Tillandsia usneoides for monitoring (133)Cs and investigated if Cs was trapped by the plant external surface structures. The results showed that T. usneoides was able to survive relatively high Cs stress. With the increase of Cs solution concentration, the total of Cs in plants increased significantly, which suggests that the plants could accumulate Cs quickly and effectively. Therefore, T. usneoides has considerable potential for monitoring Cs polluted environments. In addition, scanning electron microscopy (SEM) and energy dispersive spectrometer (EDS) analysis showed that Cs was detected in each type of cells in foliar trichomes, and the ratio of Cs in the internal disc cell was higher than that in ring cell and wing cell, which indicates that the mechanism of adsorption Cs in Tillandsia has an active component. Copyright © 2012. Published by Elsevier Inc.

  12. Experimental and computation method for determination of burnup and isotopic composition of the WWER-440 fuel using the 134Cs and 137Cs concentrations

    International Nuclear Information System (INIS)

    Babichev, B.A.; Kozharin, V.V.

    1990-01-01

    An experimental and computational method for determination of burnup and actinoid concentrations in WWER fuel elements using 134 Cs and 137 Cs concentrations in fuel is considered. It is shown that the error in calculation of fuel burnup and U and Pu isotope concentrations in WWER-440 fuel elements is 1.3-4.9% provided that the error in 134 Cs and 137 Cs concentration measurements does not exceed 1.7 and 1.2%. 9 refs.; 10 figs.; 4 tabs

  13. On the cesium-rich part of the Cs-Te phase diagram

    International Nuclear Information System (INIS)

    Boer, R. de; Cordfunke, E.H.P.

    1995-03-01

    The cesium-tellurium system in the region between 33 and 55 at.% Te has been investigated with X-ray diffraction and DSC. The existence of the compounds Cs 5 Te 3 and CsTe is demonstrated. The latter compound exhibits a structural transition at elevated temperature, as does the compound Cs 2 Te. The earlier reported compounds Cs 3 Te 2 and Cs 5 Te 4 do not exist. (orig.)

  14. Quasi-freestanding graphene on Ni(111) by Cs intercalation

    KAUST Repository

    Alattas, Maha Hassan Mohssen

    2016-05-26

    A possible approach to achieve quasi-freestanding graphene on a substrate for technological purpose is the intercalation of alkali metal atoms. Cs intercalation between graphene and Ni(111) therefore is investigated using density functional theory, incorporating van der Waals corrections. It is known that direct contact between graphene and Ni(111) perturbs the Dirac states. We find that Cs intercalation restores the linear dispersion characteristic of Dirac fermions, which agrees with experiments, but the Dirac cone is shifted to lower energy, i.e., the graphene sheet is n-doped. Cs intercalation therefore decouples the graphene sheet from the substrate except for a charge transfer. On the other hand, the spin polarization of Ni(111) does not extend through the intercalated atoms to the graphene sheet, for which we find virtually spin-degeneracy.

  15. Radiochemical determination of {sup 137}Cs in foods

    Energy Technology Data Exchange (ETDEWEB)

    Kastner, Geraldo F.; Ferreira, Andrea Vidal; Monteiro, Roberto P.G., E-mail: gfk@cdtn.br, E-mail: avf@cdtn.br, E-mail: rpgm@cdtn.br [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)

    2013-07-01

    A determination of radionuclides in food samples is important in commodities in order to attend to regulatory requirements for international trade. As a long-lived radioisotope of cesium, {sup 137}Cs is produced as a result of human nuclear activities and than its contamination level evaluation among others radionuclides in foods is necessary. A methodology for the determination of {sup 137}Cs in foods, pork and fish, is described. The procedures covered homogenization and freeze-drying of the samples. The {sup 137}Cs was measured by gamma spectrometry using Canberra 50% HPGe detector. The counting was carried out with Monte Carlo software for detection conditions optimization including geometry and chemical data information. A certified sample, SRM IAEA-375, was analyzed in order to evaluate the reliability of the method, and the results showed good agreement between the measured and certified values. (author)

  16. {sup 134}Cs emission probabilities determination by gamma spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Almeida, M.C.M. de, E-mail: candida@cnen.gov.br [Comissão Nacional de Energia Nuclear (DINOR/CNEN), Riode Janeiro, RJ (Brazil); Poledna, R.; Delgado, J.U.; Silva, R.L.; Araujo, M.T.; Silva, C.J. da [Instituto de Radioproteção e Dosimetria (LNMRI/IRD/CNEN-RJ), Rio de Janeiro, RJ (Brazil)

    2017-07-01

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

  17. Bioaccumulation of Cs-137 and Co-57 by marine phytoplankton

    International Nuclear Information System (INIS)

    Heldal, H.E.; Stupakoff, I.; Fisher, N.S.

    1999-01-01

    Under controlled laboratory conditions we have examined the bioaccumulation of Cs-137 and Co-57 in three prymnesiophytes, the coccolithophorid Emiliania huxleyi and the non-calcareous species Isochrysis galbana and Phaeocystis globosa, and two diatoms Skeletonema costatum and Thalassiosira pseudonana. We measured uptake in growing and non-growing cells, and determined concentration factors on both volume and dry weight basis. For Co-57 uptake in non-growing cells, volume concentration factors (VCF) at equilibrium ranged from 0.2 * 10 3 for Emiliana huxleyi to 4 * 10 3 for the diatom Thalassiosira pseudonana. For Cs-137 uptake in non-growing cells the VCFs were close to zero. The results suggest that, in contrast to Co, the cycling and bioaccumulation in animals of Cs in marine systems is unlikely to be affected by primary producers. (au)

  18. Medical management of the victims of Goiana 137 Cs accident

    International Nuclear Information System (INIS)

    Brandao-Mello, C.E.; Farina, R.; Oliveira, A.R.; Valverde, N.J.

    1989-01-01

    In September 1987, a radiation accident happened in Gioania due to the theft of a shielded source of 137 Cs. Fifty persons were involved showing whole-body and local acute irradiation and also external and/or internal contamination mainly due to ingestion or absorption of 137 Cs. Fourteen of fifty developed severe bone marrow depression characterized by neutropenia and thrombocytopenia. None were submitted to bone marrow transplantation. Eight of fourteen received intravenously GM-CSF. Four of the fourteen died due to hemorrhage and infection. For those with significant internal contamination, Prussian blue was administered (1.5 to 10.0 gm/per day). Besides blue, other measures were taken to increase decorporation of 137 Cs including diuretics, water overload and ergometric exercises. Radiation induced skin injuries were observed in 28 patients and were treated conservatively. 6 patients required surgical intervention. (author)

  19. Quasi-freestanding graphene on Ni(111) by Cs intercalation

    KAUST Repository

    Alattas, Maha Hassan Mohssen

    2017-01-08

    It is of technological interest to achieve quasi-freestanding graphene on a substrate. A possible approach is the intercalation of alkali metal atoms. Cs intercalation between graphene and Ni(111) is investigated using density functional theory, incorporating van der Waals corrections. It is known that direct contact between graphene and Ni(111) perturbs the Dirac states. Cs intercalation restores the linear dispersion characteristic of Dirac fermions, which is in agreement with experiments1, but the Dirac cone is shifted to lower energy, i.e., the graphene sheet is n-doped. Cs intercalation therefore effectively decouples the graphene sheet from the substrate except for a charge transfer. On the other hand, the spin polarization of Ni(111) does not extend through the intercalated atoms to the graphene sheet, for which we find virtually spin-degeneracy.

  20. Household methods to reduce {sup 137}Cs contents of mushrooms

    Energy Technology Data Exchange (ETDEWEB)

    Kostiainen, E. [Radiation and Nuclear Safety Authority - STUK, Helsinki (Finland)

    2005-09-15

    High radiocaesium contents in different species of mushrooms have been observed in areas contaminated by radiocaesium deposition after the Chernobyl accident in 1986. There has been no significant reduction in the {sup 137}Cs contents of mushrooms during the past ten years, besides via radioactive decay. The internal radiation dose received via mushrooms can be reduced by processing mushrooms before consumption. Various household methods were studied to find out their efficiency to reduce {sup 137}Cs contents of mushrooms. The methods tested were the same as normally used in cooking. The tests were made for the species of edible mushrooms widely consumed. The retention factors for the treatments tested were in most cases 0.2-0.3. The efficiency of treatments in reducing the {sup 137}Cs contents increased with larger water volumes and prolonged treatment times.

  1. Household methods to reduce 137Cs contents of mushrooms

    International Nuclear Information System (INIS)

    Kostiainen, E.

    2005-01-01

    High radiocaesium contents in different species of mushrooms have been observed in areas contaminated by radiocaesium deposition after the Chernobyl accident in 1986. There has been no significant reduction in the 137 Cs contents of mushrooms during the past ten years, besides via radioactive decay. The internal radiation dose received via mushrooms can be reduced by processing mushrooms before consumption. Various household methods were studied to find out their efficiency to reduce 137 Cs contents of mushrooms. The methods tested were the same as normally used in cooking. The tests were made for the species of edible mushrooms widely consumed. The retention factors for the treatments tested were in most cases 0.2-0.3. The efficiency of treatments in reducing the 137 Cs contents increased with larger water volumes and prolonged treatment times

  2. Zulliger (CS in Assessing the Relational Maturity of Children

    Directory of Open Access Journals (Sweden)

    Anna Elisa Villemor-Amaral

    Full Text Available Abstract Relational maturity is an important aspect to be considered in the evaluation of children. Its development in children is considered related to sex and chronological age. The present study aimed to seek evidence of validity for the Zulliger test (Comprehensive System - CS in the evaluation of maturity for interpersonal relationships in children. A total of 566 children, both sexes, of which 52.8% were girls, were submitted to the Zulliger test (CS. For comparison according to age, a subsample was extracted, composed of two groups of six and 12-year-olds, totaling 115 children. The analysis revealed statistically significant differences in the variables H, (H, A, Ad, (A, M, FC and AG. Results show findings in favor of using the Zulliger test (CS in the evaluation of maturity for interpersonal relationships in children.

  3. Studies on diffusion of 137Cs in cement mortar

    International Nuclear Information System (INIS)

    Takebe, Shinichi; Shimooka, Kenji; Wadachi, Yoshiki; Kuramoto, Yuzuru.

    1989-12-01

    Penetration experiment of 137 Cs into the impermeable cement mortar which has been treated by the impermeable reagent (XYPEX reagent) was carried out in order to advance the performance of engineered barrier for Low Level Radioactive Waste. The result showed that the radioactive concentration at deeper region in the impermeable cement mortar specimen was decreased about 1 order of magnitude below that in the untreated specimen. Diffusion coefficient calculated from the radioactive concentration of 137 Cs in the cement mortar specimen was 9.1 x 10 -5 cm 2 /day for untreated cement mortar specimen and 4.0 x 10 -5 cm 2 /day for the impermeable cement mortar specimen, respectively. Treatment of cement mortar by the impermeable reagent was found to be effective to reduce the value of appearent diffusion coefficient for 137 Cs in the cement mortar. (author)

  4. Airborne fallout mapping of 137Cs Finnish defence forces team

    International Nuclear Information System (INIS)

    Kettunen, M.; Heininen, T.; Pulakka, M.

    1997-01-01

    The main task of the team was to create a fallout map of 137 Cs in a specified area in Padasjoki Auttoinen village. The team used an MI-8 helicopter of the Finnish Air Force. The team had an HPGe system (relative efficiency 70%) to measure nuclide specific ground contamination level. For navigation the team took advantage of the DGPS service provided by Finnish Broadcasting company utilizing the RDS-channel to get position accuracy within 2 meters. The correction signal is reachable nationwide on the FM transmitter network. The system produced a distribution map for 40 K and fallout maps for 134,137 Cs using a Micro Station Program with TerraModeler application. The maximum measured 137 Cs ground contamination exceeded 130-140 kBqm -2 . (au)

  5. Measurement of thermal neutron cross section and resonance integral of the reaction {sup 135}Cs(n,{gamma}){sup 136}Cs

    Energy Technology Data Exchange (ETDEWEB)

    Katoh, Toshio; Nakamura, Shoji; Harada, Hideo [Power Reactor and Nuclear Fuel Development Corp., Tokyo (Japan); Hatsukawa, Yuichi; Shinohara, Nobuo; Hata, Kentaro; Kobayashi, Katsutoshi; Motoishi, Shoji; Tanase, Masakazu

    1997-03-01

    The thermal neutron(2,200 m/s neutron) capture cross section({sigma}{sub 0}) and the resonance integral(I{sub 0}) of the reaction {sup 135}Cs(n,{gamma}){sup 136}Cs were measured by an activation method. Targets of radioactive cesium, which include {sup 135}Cs, {sup 137}Cs and stable {sup 133}Cs, were irradiated with reactor neutrons within or without a Cd shield case. The ratio of the number of nuclei of {sup 135}Cs to that of {sup 137}Cs was measured with a quadrupole mass spectrometer. This ratio and the ratio of activity of {sup 136}Cs to that of {sup 137}Cs were used for deduction of the {sigma}{sub 0} and the I{sub 0} of {sup 135}Cs. The {sigma}{sub 0} and the I{sub 0} of the reaction {sup 135}Cs(n,{sigma}){sup 136}Cs were 8.3 {+-} 0.3 barn and 38.1 {+-} 2.6 barn, respectively. (author)

  6. Estimation of average burnup of damaged fuels loaded in Fukushima Dai-ichi reactors by using the 134Cs/137Cs ratio method

    International Nuclear Information System (INIS)

    Endo, T.; Sato, S.; Yamamoto, A.

    2012-01-01

    Average burnup of damaged fuels loaded in Fukushima Dai-ichi reactors is estimated, using the 134 Cs/ 137 Cs ratio method for measured radioactivities of 134 Cs and 137 Cs in contaminated soils within the range of 100 km from the Fukushima Dai-ichi nuclear power plants. As a result, the measured 134 Cs/ 137 Cs ratio from the contaminated soil is 0.996±0.07 as of March 11, 2011. Based on the 134 Cs/ 137 Cs ratio method, the estimated burnup of damaged fuels is approximately 17.2±1.5 [GWd/tHM]. It is noted that the numerical results of various calculation codes (SRAC2006/PIJ, SCALE6.0/TRITON, and MVP-BURN) are almost the same evaluation values of 134 Cs/ 137 Cs ratio with same evaluated nuclear data library (ENDF-B/VII.0). The void fraction effect in depletion calculation has a major impact on 134 Cs/ 137 Cs ratio compared with the differences between JENDL-4.0 and ENDF-B/VII.0. (authors)

  7. Temporal variations of Cs-137 in Sots Pine

    International Nuclear Information System (INIS)

    Nylen, T.; Plamboeck, A.H.; Boson, J.

    2008-01-01

    In this study the temporal changes in 137 Cs distribution in a Scots pine (Pinus Sylvestris L.) stand was studied during 1986 to 2006 in Northern Sweden. The Chernobyl fallout provided an excellent possibility to study the uptake and retention in conifer trees of 137 Cs, since the deposition lasted for only a few days. The average deposition of 137 Cs in the region that originates from the Chernobyl accident in 1986 was 20 ± 9 kBq M -2 . Also 137 Cs from the atmospheric nuclear weapons tests was present in the area and was only 3 ±2 kBq m -2 . Studies show that the redistribution of radioactive caesium still contribute to high activity concentrations in some compartments of the ecosystem. It has been known that certain fungi continue to produce fruit bodies with high amounts of 137 Cs. The current study adds another aspect to consider: The high activity concentration in branches and current needles during 2006 indicates an uptake of 137 Cs from the soil which could lead to concentrations in Scots Pine that has to be considered in forestry and other kind of utilization of forest products. There are for instance a few game birds such as the capercaillie (Tetrao urogallus) that feed on pine shoots. Another possible effect is on the use of pine branches in the bio fuel industry. Given an activity concentration of 1200 Bq/kg (d.w.) and a concentration factor of 10 during combustion the concentration in ashes would be 12000 bq/kg. According to the recommendations from SSI (the Swedish Radiation Protection Authority) ashes that have concentrations higher than 10 kBq/kg must be stored in special deposits. It would be of interest to investigate the uptake in stands of different ages since the pine stand that was studied was about 30 years old in 1986 and do not represent neither a mature nor a newly established stand (tk)

  8. Development of the CsI Calorimeter Subsystem for AMEGO

    Science.gov (United States)

    Grove, J. Eric; Woolf, Richard; Johnson, W. Neil; Phlips, Bernard

    2018-01-01

    We report on the development of the thallium-doped cesium iodide (CsI:Tl) calorimeter subsystem for the All-Sky Medium-Energy Gamma-ray Observatory (AMEGO). The CsI calorimeter is one of the three main subsystems that comprise the AMEGO instrument suite; the others include the double-sided silicon strip detector (DSSD) tracker/converter and a cadmium zinc telluride (CZT) calorimeter. Similar to the LAT instrument on Fermi, the hodoscopic calorimeter consists of orthogonally layered CsI bars. Unlike the LAT, which uses PIN photodiodes, the scintillation light readout from each end of the CsI bar is done with recently developed large-area silicon photomultiplier (SiPM) arrays. We currently have an APRA program to develop the calorimeter technology for a larger, future space-based gamma-ray observatory. Under this program, we are building and testing a prototype calorimeter consisting of 24 CsI bars (16.7 mm x 16.7 mm x 100 mm) arranged in 4 layers with 6 bars per layer. The ends of each bar are read out with a 2 x 2 array of 6 mm x 6 mm SensL J series SiPMs. Signal readout and processing is done with the IDEAS SIPHRA (IDE3380) ASIC. Performance testing of this prototype will be done with laboratory sources, a beam test, and a balloon flight in conjunction with the other subsystems led by NASA GSFC. Additionally, we will test 16.7 mm x 16.7 mm x 450 mm CsI bars with SiPM readout to understand the performance of longer bars in advance of the developing the full instrument.Acknowledgement: This work was sponsored by the Chief of Naval Research (CNR) and NASA-APRA (NNH15ZDA001N-APRA).

  9. Distribution of 137Cs in environmental soil and crude drugs

    International Nuclear Information System (INIS)

    Kimura, Shoujiro; Yamaoki, Rumi

    1997-01-01

    Radioactivity of 137 Cs and 40 K was determined on commercially available products of Houttuynia Herb which were imported from China and Taiwan or processed in Japan, and of Houttuynia cordata harvested in 15 places in Japan and the surrounding soil. On Houttuynia Herb, the concentrations of 137 Cs and 40 K were LTD (less than detectable)-7.6 Bq/kg dry and 743-1964 Bq/kg dry, respectively, suggesting than the concentration of 137 Cs was less than 1% of that of 40 K. The domestic products were found to contain higher concentrations of 137 Cs and 40 K than the imported ones. The concentration of 137 Cs of Houttuynia cordata harvested in Japan ranged from 0.8 Bq/kg dry to 172 Bq/kg dry, while the concentration of 40 K was almost the same as that of the commercial products. The concentration ratio of 40 K in Houttuynia cordata to that in the soil was correlated with the moisture content and the ignition loss of the soil. However, the concentration ratio of 137 Cs did not show a very clear correlation. When 15 g of Houttuynia Herb or Houttuynia cordata was daily decocted and given for 1 year the former showed the committed dose equivalent of 0.02-0.5 μSv and the latter 0.06-12 μSv. Both of these values were less than 0.5% of the annual effective dose equivalent from the nature, 2.4 mSv. (author)

  10. Changes in 137Cs transfer to agricultural products

    International Nuclear Information System (INIS)

    Goncharov, N.; Timochtchenko, A.; Milutin, A.

    1999-01-01

    The food production and food harvesting systems common in the areas contaminated by the Chernobyl accident in Republic of Belarus can be grouped into three major categories: collective farm produce, private farming produce and natural foods collected from natural ecosystems. The collective farm system provided the smallest contribution (8-12 %) to the intake of 137 Cs. Natural food was the major contributor to the intake at one study site (73 %), and private produce was the major contributor (60 %) at the other study site. Assessment of the situation just after the accident (one year) shows that collective farming was still a minor contributor to 137 CS intake (10 %) whilst private fanning would have been the major contributor wherever private milk production and consumption continued. The extent to which inhabitants consume natural foods from forests has a considerable effect on their 137 CS intake. The comparative importance of food products from natural ecosystems increases with time due to the long effective ecological half lives of 137 Cs in unimproved pastures and forests. Estimation of the contribution to the fluxes of 137 Cs from the different production and harvesting systems showed that the contribution from private farming and food harvesting from natural ecosystems may also be significant, contributing 14-30 % to the total fluxes of 137 Cs from an area even if the quantity of food produced in these systems is small. However, the major contributor to the flux exported from an area was the collective farming system, accounting for about 70-86 % of the total. Refs. 12 (author)

  11. Parameters Affecting 137Cs Migration within Soil Profile

    International Nuclear Information System (INIS)

    Sefien, S.M.; Ibrahim, A.S.; Abdelmalik, W.E.Y.

    2013-01-01

    Some studies have been carried out on the adsorption, distribution and migration of 137 Cs within soils of the area in the vicinity of the Nuclear Research Centre, Egypt, and Ismailia Canal. The soil physicochemical and mineralogical characteristics were carried out and indicated that the soil samples consisted mainly of sand fraction (quartz) and silt fractions (semctite minerals). The kinetics of caesium adsorption and its adsorption isotherms for the tested soils were also studied. The sorption of 137 Cs on soil minerals markedly affects its migration rate. The natural background of both locations of study indicated that the amounts of 137 Cs present in the reactor site were found to be originated from the fallout and from the external contamination which affected the background level. The 137 Cs activity at the canal site was found to be 20.01 Bq/m 2 .cm, while that around the reactor site were found to be 231.15 Bq/m2.cm which may be originating from the fallout and from external contamination which affect the background level at that location. The activity in the canal soil which amounted to 20.01 Bq/m2/cm (0.87 Bq/kg) is about that of background.Based on the distribution data, the vertical distribution of 137 Cs has been studied for soil in both locations (the vicinity of the Nuclear Research Centre (NRC) and Ismailia canal). The vertical migration rates of 137 Cs were calculated for soil samples selected from different locations. These rates were found to be 0.056 and 0.031 cm/year for the reactor and canal site respectively.

  12. Inventories and fluxes of 137Cs in the Syrian land

    International Nuclear Information System (INIS)

    Al-Masri, M. S.; Amin, Y.

    2005-03-01

    Cesium-137 inventories and atmospheric fluxes have been determined using radiocesium distributions in undistributed soil profiles, collected from 38 sites distributed all over the Syrian lands. Results have shown that 137 Cs inventories determination by Soil Layers Sum Method is more accurate than the Integration Method, where the best curve fitting of 137 Cs distribution with depth is difficult to establish. 137 Cs inventories ranged from 441 Bq.m - 2 and 13312 Bq.m - 2 using the Layers Sum Method with a mean value of 3679 Bq.m - 2; the highest values observed were in the coastal, middle and north east regions. This is due to the fact that most of Chernobyl accident atmospheric fall-out of cesium 137 had entered the Syrian land came from the west boarders (Mediterranean sea). While the lowest values were found to be in the samples collected from the east south region. In addition, 137 Cs flux ranged from 3.1 kBq m - 2y - 1 and 527.8 kBq m - 2 y - 1 with a mean value of 65.7 kBq m - 2y - 1. Moreover, there was a semi linear relationship found between 137 Cs flux and the height above sea level. While no linear relationship was found between 137 Cs flux and annual rainfall. On the other hand, the external radiation dose to Syrians that due to gamma-rays emitted from cesium 137 decay has been determined and reached a mean value of 166μ Sv.y - 1. This value is about 20% of the radiation dose received by the Syrian from naturally occurring radionuclides in soil. (Author)

  13. 210Pb-137Cs dating of glacial lake sediments

    International Nuclear Information System (INIS)

    Graham, I.J.; Ditchburn, R.G.; Barry, B.J.

    2004-01-01

    Sediments deposited in New Zealand lakes in the recent past provide excellent archives of local climate change via their trapped biodiversity, varve structure ad sedimentological composition. To unlock the archival information, accurate and fine-scale dating of the deposits is essential. A combination of 210 Pb and 137 Cs dating provides the most reliable and robust approach. Under favourable conditions, 210 Pb dating can provide a detailed chronology to c.120-140 y, and can be accurately calibrated by 137 Cs for the last 40 y or thereabouts. (author). 6 refs., 4 figs

  14. Simulation of remediation alternatives for a 137Cs contaminated soil

    International Nuclear Information System (INIS)

    Bea, S.A.; Carrera, J.; Saaltink, M.; Soler, J.M.; Ayora, C.

    2004-01-01

    We analyze remediation alternatives for a soil contaminated with 137 Cs, which sorbs strongly to clay aggregates where water flux is negligible. The mobile portion of the soil (macropores) retains little water and cesium. Some of the remediation alternatives involve infiltration of seawater enriched with KCl, to promote mobilization of Cs through exchange with K. Therefore, a fully coupled reactive transport model is used to test these alternatives. We conclude that flushing is a viable alternative, provided that some recommendations, derived from the modelling exercise are followed. These include high rate periodic infiltration and draining, as well as performing infiltration from independent cells to limit the effect of preferential flowpaths. (orig.)

  15. Linhchi mushrooms as biological monitors for 137Cs pollution

    International Nuclear Information System (INIS)

    Tran Van, L.; Le Duy, T.

    1991-01-01

    Radioactivity of Linhchi mushrooms (Ganoderma Lucidum) cultivated in laboratory and production conditions has been measured in the Environmental Laboratory of Nuclear Research Institute (NRI), Dalat, Vietnam. The results showed that Linhchi mushroom has a high radioactive concentration of 137 Cs, which is about 20 Bq kg -1 fresh weight. In addition, the radioactive contents of substrata before and after cultivation were insignificant. This suggested that Linhchi mushroom should only accumulate the 137 Cs radioisotope from the atmosphere, directly. Therefore, it should be considered as a bio-indicator for environmental monitoring. (author) 13 refs.; 3 figs.; 2 tabs

  16. Determination of Sr-90 and Cs-137 in environmental samples

    International Nuclear Information System (INIS)

    Anon.

    1987-01-01

    The comparison between the Ca concentration in the soil and the transfer factors involved indicates a clear dependence of Sr-90 soil-to-plant transport from the soil's Ca-content with the concentration level of 0.1 g Ca/kg soil appearing to be the limit level. Soil concentrations of Cs-137 determined to-date indicate a very even deposition density of Cs-137. The transfer factors of plant/soil in Chile differ but negligeably from those in Europe. (DG) [de

  17. {sup 137}Cs in a raised bog in central Sweden

    Energy Technology Data Exchange (ETDEWEB)

    Rosen, K. [Department of Soil and Environment, Swedish University of Agricultural Sciences, SLU, Ulls vag 17, Box 7014, SE-75007, Uppsala (Sweden)], E-mail: klas.rosen@mv.slu.se; Vinichuk, M. [Department of Soil and Environment, Swedish University of Agricultural Sciences, SLU, Ulls vag 17, Box 7014, SE-75007, Uppsala (Sweden); Department of Ecology, Zhytomyr State Technological University, 103 Cherniakhovsky Str., 10005 Zhytomyr (Ukraine); Johanson, K.J. [Department of Soil and Environment, Swedish University of Agricultural Sciences, SLU, Ulls vag 17, Box 7014, SE-75007, Uppsala (Sweden)

    2009-07-15

    The vertical distribution of {sup 137}Cs activity in peat soil profiles and {sup 137}Cs activity concentration in plants of various species was studied in samples collected at two sites on a raised bog in central Sweden. One site (open bog) was in an area with no trees and only a few sparsely growing plant species, while the other (low pine) was less than 100 m from the open bog site and had slowly growing Scots pine, a field layer dominated by some ericaceous plants and ground well-covered by plants. The plant samples were collected in 2004-2007 and were compared with samples collected in 1989 from the same open bog and low pine sites. Ground deposition of {sup 137}Cs in 2005 was similar at both sites, 23 000 Bq m{sup -2}. In the open bog peat profile it seems to be an upward transport of caesium since a clear peak of {sup 137}Cs activity was found in the uppermost 1-4 cm of Sphagnum layers, whereas at the low pine site {sup 137}Cs was mainly found in deeper (10-12 cm) layers. The migration rate was 0.57 cm yr{sup -1} at the open bog site and the migration centre of {sup 137}Cs was at a depth of 10.7, while the rate at the low pine site was 0.78 cm yr{sup -1} and the migration centre was at 14.9 cm. Heather (Calluna vulgaris) was the plant species with the highest {sup 137}Cs activity concentrations at both sites, 43.5 k Bq{sup -1} DM in 1989 decreasing to 20.4 in 2004-2007 on open bog and 22.3 k Bq kg{sup -1} DM in 1989 decreasing to 11.2 k Bq{sup -1} DM by the period 2004-2007 on the low pine site. {sup 137}Cs transfer factors in plants varied between 0.88 and 1.35 on the open bog and between 0.48 and 0.69 m{sup 2} kg{sup -1} DM at the low pine site.

  18. Mechanisms and models of 137Cs migration in soil

    International Nuclear Information System (INIS)

    Frid, A.S.

    1999-01-01

    The most wide-spread mechanisms and models of the 137 Cs isotope migration in soil are considered because of urgency of this problem conditioned by global fallout during nuclear weapon tests and contamination of territories due to accidents on nuclear objects (including the East Urals and ChNPP accident). It is shown that the 137 Cs migration models with an account of the sorption-desorption kinetics have from the practical adequacy certain advantage in comparison with other models, though they are mathematically more complex and require complex calculations [ru

  19. 137Cs in a raised bog in central Sweden

    International Nuclear Information System (INIS)

    Rosen, K.; Vinichuk, M.; Johanson, K.J.

    2009-01-01

    The vertical distribution of 137 Cs activity in peat soil profiles and 137 Cs activity concentration in plants of various species was studied in samples collected at two sites on a raised bog in central Sweden. One site (open bog) was in an area with no trees and only a few sparsely growing plant species, while the other (low pine) was less than 100 m from the open bog site and had slowly growing Scots pine, a field layer dominated by some ericaceous plants and ground well-covered by plants. The plant samples were collected in 2004-2007 and were compared with samples collected in 1989 from the same open bog and low pine sites. Ground deposition of 137 Cs in 2005 was similar at both sites, 23 000 Bq m -2 . In the open bog peat profile it seems to be an upward transport of caesium since a clear peak of 137 Cs activity was found in the uppermost 1-4 cm of Sphagnum layers, whereas at the low pine site 137 Cs was mainly found in deeper (10-12 cm) layers. The migration rate was 0.57 cm yr -1 at the open bog site and the migration centre of 137 Cs was at a depth of 10.7, while the rate at the low pine site was 0.78 cm yr -1 and the migration centre was at 14.9 cm. Heather (Calluna vulgaris) was the plant species with the highest 137 Cs activity concentrations at both sites, 43.5 k Bq -1 DM in 1989 decreasing to 20.4 in 2004-2007 on open bog and 22.3 k Bq kg -1 DM in 1989 decreasing to 11.2 k Bq -1 DM by the period 2004-2007 on the low pine site. 137 Cs transfer factors in plants varied between 0.88 and 1.35 on the open bog and between 0.48 and 0.69 m 2 kg -1 DM at the low pine site.

  20. Solving PDEs in Python the FEniCS tutorial I

    CERN Document Server

    Langtangen, Hans Petter

    2016-01-01

    This book offers a concise and gentle introduction to finite element programming in Python based on the popular FEniCS software library. Using a series of examples, including the Poisson equation, the equations of linear elasticity, the incompressible Navier–Stokes equations, and systems of nonlinear advection–diffusion–reaction equations, it guides readers through the essential steps to quickly solving a PDE in FEniCS, such as how to define a finite variational problem, how to set boundary conditions, how to solve linear and nonlinear systems, and how to visualize solutions and structure finite element Python programs. This book is open access under a CC BY license.

  1. Mathematical model of 137Cs dynamics in the deciduous forest

    International Nuclear Information System (INIS)

    Mamikhin, S.V.; Klyashtorin, A.L.

    1999-01-01

    A mathematical model of 137 Cs behaviour in the forest ecosystem is presented. The behaviour of this radionuclide is assumed to obey the same regularities as the behaviour of its stable chemical analogue, potassium. Radionuclide dynamics are considered in parallel with the dynamics of the phytomass. Radionuclides contained in the vegetation are pooled into two basic compartments: external and internal contamination, with separate analysis of each. The model was verified using the data obtained in the 30-km zone of the Chernobyl NPP in 1986-1994. The algorithm described was found to be the most efficient in terms of 137 Cs behaviour in the forest environments

  2. Low-temperature anharmonicity in cesium chloride (CsCl)

    Energy Technology Data Exchange (ETDEWEB)

    Sist, Mattia; Faerch Fischer, Karl Frederik; Brummerstedt Iversen, Bo [Center for Materials Crystallography, Department of Chemistry and iNANO, Aarhus University (Denmark); Kasai, Hidetaka [Center for Materials Crystallography, Department of Chemistry and iNANO, Aarhus University (Denmark); Faculty of Pure and Applied Sciences, TIMS and CiRfSE, University of Tsukuba (Japan)

    2017-03-20

    Anharmonic lattice vibrations govern heat transfer in materials, and anharmonicity is commonly assumed to be dominant at high temperature. The textbook cubic ionic defect-free crystal CsCl is shown to have an unexplained low thermal conductivity at room temperature (ca. 1 W/(m K)), which increases to around 13 W/(m K) at 25 K. Through high-resolution X-ray diffraction it is unexpectedly shown that the Cs atomic displacement parameter becomes anharmonic at 20 K. (copyright 2017 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

  3. Transfer factor values of 137 Cs from latosoils to vegetables

    International Nuclear Information System (INIS)

    Wasserman, Maria Angelica Moreira; Belem, Lilia Maria Juacaba

    1996-01-01

    Transfer Factor values for black beams, radish and carrot were obtained for soils artificially and accidentally contaminated in Goiania during 1987. Differences of 137 Cs-soil-to-plant transfer were discussed in the light of pedology and crop type. These values were about one order of magnitude higher than mean values reported by IUR for temperature climate for the same crops. These results advertising for the peculiar dynamics of 137 Cs in tropical soils and for needs to obtain regional data to be used in assessment dose models. (author)

  4. Laser Decontamination of Surfaces Contaminated with Cs+ Ion

    International Nuclear Information System (INIS)

    Baigalmaaa, B.; Won, H. J.; Moon, J. K.; Jung, C. H.; Lee, K. W.; Hyun, J. H.

    2008-01-01

    Laser decontamination technology has been proven to be an efficient method for a surface modification of metals and concretes contaminated with radioactive isotopes. Furthermore, the generation of a secondary waste is negligible. The radioactivity of hot cells in the DFDF (Dupic Fuel Development Facility) is presumed to be very high and the predominant radionuclide is Cs-137. A series of laser decontamination studies by a fabricated Q-switched Nd:YAG laser system were performed on stainless steel specimens artificially contaminated with Cs+ ion. Decontamination characteristics of the stainless steel were analyzed by SEM and EPMA

  5. Flash CS5.5 The Missing Manual

    CERN Document Server

    Grover, Chris

    2011-01-01

    You can build everything from simple animations to full-fledged iOS and Android apps with Flash CS5.5, but learning this complex program can be difficult-unless you have this fully updated, bestselling guide. Learn how to create gorgeous Flash effects even if you have no programming experience. With Flash CS5.5: The Missing Manual, you'll move from the basics to power-user tools with ease. Learn animation basics. Discover how to turn simple ideas into stunning animations.Master Flash's tools. Learn the animation and effects tools with clear explanations and hands-on examples.Use 3D effects. R

  6. CsI calorimeter of the CMD-3 detector

    International Nuclear Information System (INIS)

    Aulchenko, V.M.; Bondar, A.E.; Erofeev, A.L.; Kovalenko, O.A.; Kozyrev, A.N.; Kuzmin, A.S.; Logashenko, I.B.; Razuvaev, G.P.; Ruban, A.A.; Shebalin, V.E.; Shwartz, B.A.; Talyshev, A.A.; Titov, V.M.; Yudin, Yu.V.; Epifanov, D.A.

    2015-01-01

    The VEPP-2000 e + e − collider has been operated at Budker Institute of Nuclear Physics since 2010. The experiments are performed with two detectors CMD-3 and SND. The calorimetry at the CMD-3 detector is based on three subsystems, two coaxial barrel calorimeters—Liquid Xenon Calorimeter and crystal CsI calorimeter, and endcap calorimeter with BGO crystals. This paper describes the CsI calorimeter of the CMD-3 detector. The calorimeter design, its electronics and calibration procedures are discussed

  7. A winning combination: the 3Cs of business continuity.

    Science.gov (United States)

    Glendon, Lee

    2013-01-01

    Contingency planning is a natural part of business life and is used across identified strategic, financial and operational risks. But is it being done well and is it the right approach all of the time? This paper shows how contingency planning forms one layer of a three-line defence termed 'the 3Cs of business continuity': contingency planning; continuity capability; crisis response. Collectively, 'the 3Cs' help organisations deliver a robust response to the risks that can be seen and those that cannot.

  8. Cs adsorption on the clay-sized fraction of various soils: effect of organic matter destruction and charge compensating cation

    International Nuclear Information System (INIS)

    Staunton, S.; Levacic, P.

    1999-01-01

    The association of organic matter with clay minerals may decrease their affinity for Cs and thus enhance its bioavailability. We have investigated this hypothesis by comparing Cs adsorption on several soils, both topsoils and the corresponding subsoils, before and after organic matter destruction with H 2 O 2 . The clay-sized fractions were homoionic in either K, Na or Ca, to avoid artefacts due to variable composition of the exchange complex. All experiments were carried out in dilute suspension under controlled conditions. The affinity of the clay-sized fractions for Cs and the value of the Freundlich b parameter are typical of illites. This supports the hypothesis that the adsorption properties of soils are dominated by small amounts of illite. However, if this is the case, the affinity of soil illites is higher than that of reference illites. The destruction of organic matter has a variable effect. In some cases, a marked enhancement is observed, in others there is no significant effect, or a small decrease. There is no clear pattern relating the effect of organic matter destruction and either dominant clay mineralogy or organic matter content. (Copyright (c) 1999 Elsevier Science B.V., Amsterdam. All rights reserved.)

  9. Recent levels of radionuclides in lichens from southwest Poland with particular reference to 134Cs and 137Cs

    International Nuclear Information System (INIS)

    Seaward, M.R.D.; Bylinska, E.A.

    1988-01-01

    Analyses of Umbilicaria species collected from southwest Poland in August 1986 have shown there to be significant increases in levels of various radionuclides since previous analyses based on fieldwork in 1978-1979. The composition and ratio of the various radionuclides, particularly in respect of 134 Cs and 137 Cs, exhibit a characteristic signature consistent with contamination derived from the accident at the Chernobyl nuclear reactor in April 1986. Intraspecific variation in levels of 137 Cs in Umbilicaria is related to such factors as location, altitude and, to a lesser degree, aspect; interspecific variation in levels is related to ecological requirements and geographical pattern, and hence the same factors, although morphological differences in thalli may be implicated. (author)

  10. Elastic properties of Cs2HgBr4 and Cs2CdBr4 crystals

    International Nuclear Information System (INIS)

    Kityk, A.V.; Zadorozhna, A.V.; Shchur, Y.I.; Martynyuk-Lototska, Y.I.; Burak, Y.; Vlokh, O.G.

    1998-01-01

    Using ultrasonic velocity measurements, all components of the elastic constant matrix C ij , elastic compliances matrix S ij , and linear compressibility constants matrix K ij of orthorhombic Cs 2 HgBr 4 and Cs 2 CdBr 4 crystals have been determined over a wide temperature range, including the region of the phase transition from the normal to the incommensurate phase. Results obtained are considered within the framework of the phenomenological theory. Preliminary analysis of the acoustical properties at room temperature clearly indicates that both crystals are relatively important materials for acousto-optical applications. Copyright (1998) CSIRO Australia

  11. Exposure of a herbivorous fish to 134Cs and 137Cs from the riverbed following the Fukushima disaster

    International Nuclear Information System (INIS)

    Tsuboi, Jun-ichi; Abe, Shin-ichiro; Fujimoto, Ken; Kaeriyama, Hideki; Ambe, Daisuke; Matsuda, Keishi; Enomoto, Masahiro; Tomiya, Atsushi; Morita, Takami; Ono, Tsuneo; Yamamoto, Shoichiro; Iguchi, Kei'ichiro

    2015-01-01

    Ayu Plecoglossus altivelis, a herbivorous fish, is an important fishery resource and key component of the foodweb in many Japanese streams. Radionuclide contamination of this species is likely transferred to higher trophic levels, include humans, in the food chain. After the Fukushima accident in March 2011, ayu were exposed to highly contaminated silt while feeding on algae attached to the riverbed stones. To understand the route by which herbivorous fish are exposed to radionuclides, the activity concentrations of sum of 134 Cs and 137 Cs (radiocesium) were analyzed in riverbed samples (algae and silt) and in the internal organs and the muscle of ayu in five river systems in the Fukushima Prefecture between summer 2011 and autumn 2013. Although there was a positive correlation between the radiocesium activity concentrations in the muscle and the internal organs of ayu, the median activity concentration in the muscle was much lower than those in the internal organs. The activity concentrations of radiocesium in the riverbed samples and the internal organs and the muscle of ayu were correlated with contamination levels in soil samples taken from the watershed upstream of the sample sites. The results of the generalized linear mixed models suggest that the activity concentrations in both the internal organs and the muscle of ayu declined over time. Additionally, the activity concentrations in the internal organs were correlated with those in the riverbed samples that were collected around the same time as the ayu. The activity concentrations in the muscle were correlated with ayu body size. Our results suggest that ayu ingest 134 Cs and 137 Cs while grazing silt and algae from the riverbed, and a part of the 134 Cs and 137 Cs is assimilated into the muscle of the fish. - Highlights: • The radiocesium (sum of 134 Cs and 137 Cs) concentrations in a herbivorous fish were measured following the Fukushima disaster. • The muscle concentrations were correlated with

  12. Satellite bands of the RbCs molecule in the range of highly excited states

    Energy Technology Data Exchange (ETDEWEB)

    Rakić, Mario; Beuc, Robert; Skenderović, Hrvoje, E-mail: hrvoje@ifs.hr [Institute of Physics, Bijenička cesta 46, Zagreb 10000 (Croatia); Bouloufa-Maafa, Nadia; Dulieu, Olivier; Vexiau, Romain [Laboratoire Aimé Cotton, CNRS, Université Paris-Sud, ENS Cachan, Université Paris-Saclay, Bât. 505, Campus d’Orsay, Orsay Cedex 91405 (France); Pichler, Goran [Physics Department, Kuwait University, PO Box 5969, Safat—13060 (Kuwait)

    2016-05-28

    We report on the observation of three RbCs satellite bands in the blue and green ranges of the visible spectrum. Absorption measurements are performed using all-sapphire cell filled with a mixture of Rb and Cs. We compare high resolution absorption spectrum of Rb-Cs vapor mixture with pure Rb and Cs vapor spectra from the literature. After detailed analysis, the new satellite bands of RbCs molecule at 418.3 nm, 468.3, and 527.5 nm are identified. The origin of these bands is discussed by direct comparison with difference potentials derived from quantum chemistry calculations of RbCs potential energy curves. These bands originate from the lower Rydberg states of the RbCs molecule. This study thus provides further insight into photoassociation of lower Rydberg molecular states, approximately between Cs(7s) + Rb(5s) and Cs(6s) + Rb(6p) asymptotes, in ultracold gases.

  13. Distribution of 137Cs Radionuclide in Industrial Wastes Effluents of Gresik, East Java, Indonesia

    Directory of Open Access Journals (Sweden)

    Muslim

    2015-04-01

    Full Text Available The distribution of anthropogenic radionuclides 137Cs was measured from industrial waste effluent of Gresik to Gresik Sea in east Java, Indonesia. The activity of 37Cs detected at all stations was much lower than in northeast Japan both before and after NPP Fukushima accident. This indicated that in Gresik industrials waste did not consist of 137Cs. The lowest activity 137Cs occurred at the station nearest to the industrial waste effluent that contained some particle ions that were able to scavenge 137Cs and then precipate this radionuclide. Furthermore, the greatest 137Cs occured at the station that has high current speeds that stirred up sediment to release 137Cs in seawater as a secondary source. The lowest salinity did not effect on the activity of 137Cs even though the lowest salinity and activity 137Cs occured at the same station

  14. Early stages of Cs adsorption mechanism for GaAs nanowire surface

    Science.gov (United States)

    Diao, Yu; Liu, Lei; Xia, Sihao; Feng, Shu

    2018-03-01

    In this study, the adsorption mechanism of Cs adatoms on the (100) surface of GaAs nanowire with [0001] growth direction is investigated utilizing first principles method based on density function theory. The adsorption energy, work function, atomic structure and electronic property of clean surface and Cs-covered surfaces with different coverage are discussed. Results show that when only one Cs is adsorbed on the surface, the most favorable adsorption site is BGa-As. With increasing Cs coverage, work function gradually decreases and gets its minimum at 0.75 ML, then rises slightly when Cs coverage comes to 1 ML, indicating the existence of 'Cs-kill' phenomenon. According to further analysis, Cs activation process can effectively reduce the work function due to the formation of a downward band bending region and surface dipole moment directing from Cs adatom to the surface. As Cs coverage increases, the conduction band minimum and valence band maximum both shift towards lower energy side, contributed by the orbital hybridization between Cs-5s, Cs-5p states and Ga-4p, As-4s, As-4p states near Fermi level. The theoretical calculations and analysis in this study can improve the Cs activation technology for negative electron affinity optoelectronic devices based on GaAs nanowires, and also provide a reference for the further Cs/O or Cs/NF3 activation process.

  15. Coprecipitation of mono-, di-, tri-, tetra- and hexavalent ions with Na-polyuranates

    International Nuclear Information System (INIS)

    Diaz Arocas, P.; Garcia-Serrano, J.; Quinones, J.; Geckeis, H.; Grambow, B.

    1996-01-01

    The objective of this work is to study the solubility and coprecipitation phenomena related to spent fuel dissolution under anoxic conditions in order to identify potential upper limits of radionuclide release. In the present work it is attempted to identify those elements for which coprecipitation phenomena are significant. The pH dependent precipitation behaviour of minor elements with Na-polyuranates is studied in carbonate-free 5 m NaCl solutions. Three different systems were investigated: ''System A'' NaCl-Cs-Sr-Eu-Mo-Th-U(VI)-H 2 O. ''System B'' NaCl-Cs-Sr-Eu-Mo-Th-H 2 O. ''System C'' an aqueous solution of dissolved SIMulated FUEL (SIMFUEL) containing: NaCl-Sr-Ba-Y-La-Ce-Nd-Zr-Pd-Mo-Rh-Ru-U(VI)-H 2 O. The experimental results obtained in this work show that: (1) The presence of minor elements do not influence the precipitation of Na-polyuranate, (2) Solution concentration of trivalent rare Earth elements reveal a strong decrease with pH, possibly controlled by coprecipitation, (3) Tetravalent elements such as Th (Sys. A and B) and Zr (sys. C) show a strong decrease in their concentration independent of pH. Th concentrations were not controlled by coprecipitation but probably by formation of individual solubility controlling phase such as Th(OH) 4 , (4) Sr and Cs stay in solution during the precipitation process. (orig.)

  16. Color centers in heavily irradiated CsI(Tl) crystals

    International Nuclear Information System (INIS)

    Yakovlev, V.; Meleshko, A.; Trefilova, L.

    2008-01-01

    The absorption and luminescence properties of CsI(Tl) crystals colored by irradiation are studied by the method of the time-resolved spectroscopy. The scheme of the electron transitions in CsI(Tl) crystal is suggested to explain the appearance of the color centers under exposure to the near-UV light. It is established that either of the two types activator color centers holds the charge carrier with opposite sign. The model of the hole Tl 2+ v c - activator color center is suggested. According to the model the positive charge of Tl 2+ ion is compensated by the negative charge of a close cation vacancy v c - . The color center emission reveals in the cathode-luminescence spectrum of the colored CsI(Tl) crystal. The high-dose irradiation of CsI(Tl) crystal results in the reduction of the decay time of the near-thallium self-trapped excitons (STE) emission. The decay kinetics of Tl 2+ v c - emission contains the time components typical for the decay kinetics of near-thallium STE emission. The reason of the observed effects is the energy transfer from the near-thallium STE excitons to the color centers via the inductive-resonant mechanism

  17. Obstacles to superconductivity in CsCl phases

    International Nuclear Information System (INIS)

    Matthias, B.T.; Corenzwit, E.; Vandenberg, J.M.; Barz, H.; Maple, M.B.; Shelton, R.N.

    1976-01-01

    Reasons are put forward for why the CsCl structure is not a structure which is favorable for high-temperature superconductivity. The transition temperatures of several binary and ternary intermetallic compounds are given to illustrate the arguments. (B.R.H.)

  18. Theory of field induced incommensurability: CsFeCl3

    DEFF Research Database (Denmark)

    Lindgård, Per-Anker

    1986-01-01

    Using correlation theory for the singlet-doublet magnet CsFeCl3 in a magnetic field, a field induced incommensurate ordering along K-M is predicted without invoking dipolar effects. A fully self-consistent RPA theory gives Hc=44 kG in agreement with experiments at T=1.3K. Correlation and dipolar...

  19. 137Cs in the fungal compartment of Swedish forest soils

    International Nuclear Information System (INIS)

    Vinichuk, Mykhaylo M.; Johanson, Karl J.; Taylor, Andy F.S.

    2004-01-01

    The 137 Cs activities in soil profiles and in the mycelia of four ectomycorrhizal fungi were studied in a Swedish forest in an attempt to understand the mechanisms governing the transfer and retention of 137 Cs in forest soil. The biomass of four species of fungi was determined and estimated to be 16 g m -2 in a peat soil and 47-189 g m -2 in non-peat soil to the depth of 10 cm. The vertical distribution was rather homogeneous for two species (Tylospora spp. and Piloderma fallax) and very superficial for Hydnellum peckii. Most of the 137 Cs activity in mycelium of non-peat soils was found in the upper 5 cm. Transfer factors were quite high even for those species producing resupinate sporocarps. In the peat soil only approximately 0.3% of the total 137 Cs inventory in soil was found in the fungal mycelium. The corresponding values for non-peat soil were 1.3, 1.8 and 1.9%

  20. Experimental probe into adsorption of Sr, Cs in the Soil

    International Nuclear Information System (INIS)

    Yuan Guangyu; Bai Qingzhong

    1987-12-01

    There are some obstacles in researching on the adsorption patterns of Sr and Cs in soil. One of them is that it is difficult to compare and to consult between various results and data for different types and sizes of soil. For this reason, it is neccesary to do further research into adsorption patterns of Sr and Cs in single particles of soil. By using scanning electromicroscope, the microcosmic phenomena of nuclides adsorption is observed, and a possible mechanism is proposed. A certain amount of diluvial soil from Shanxi Province and a certain amount of alluvial soil from western Beijing suburban were chosen as detected samples. After determining the distributions of adsorbed Sr and Cs in varied mineral particles, it is pointed out that the defference of chemical components of various size soils effects Kd value of Sr and Cs obviously. The method for calculating Kd value of mixing samples according to the particle distribution coefficients are derived under the condition of surface adsorption as main. The authors expound that it is favourable for accuracy to select and control the particle sizes in static adsorptional experiment

  1. Interlaboratory comparison on 137Cs activity concentration in fume dust

    International Nuclear Information System (INIS)

    Tzika, Faidra; Hult, Mikael; Burda, Oleksiy; Arnold, Dirk; Sibbens, Goedele; Caro Marroyo, Belén; Gómez–Mancebo, Maria Belén; Peyrés, Virginia; Moser, Hannah; Ferreux, Laurent; Šolc, Jaroslav; Dryák, Pavel; Fazio, Aldo; Luca, Aurelian; Vodenik, Branko; Reis, Mario

    2015-01-01

    A comparison was conducted, between 11 European National Metrology Institutes and EC-JRC, on measurement of 137 Cs activity concentration in fume dust. As test material an activity standard produced from real contaminated fume dust was used. The standard material consisted of 13 cylindrical samples of compressed fume dust. The material contained 137 Cs and 60 Co of reference activity concentrations of (9.72±0.10) Bq/g and (0.450±0.018) Bq/g, respectively, for the reference date of 1 June 2013, determined using the comparison results. The organization and results of the intercomparison, as well as the process of obtaining reliable reference values are presented. - Highlights: • A European comparison was conducted on measurement of 137 Cs activity in fume dust. • Participants used high resolution gamma ray spectrometry. • Efficiency calibration included Monte Carlo, numerical and experimental methods. • Reference 137 Cs and 60 Co activity concentrations in the fume dust were determined. • A new traceable activity standard of fume dust matrix is available to end-users.

  2. Plutonium and Cs-137 in autopsy tissues in Great Britain

    International Nuclear Information System (INIS)

    Popplewell, D.S.; Ham, G.J.; Dodd, N.J.; Shuttler, S.D.

    1988-01-01

    Tissues removed at autopsy from members of the general public contain significantly higher concentrations of plutonium and 137 Cs in west Cumbrians than in people from three other regions of Great Britain. Several autopsy cases from Cumbria showed unusually high values of plutonium. Subsequently it was found that the subjects had been former employees of British Nuclear Fuels. 7 refs.; 8 tabs

  3. Airborne Gravity: NGS' Gravity Data for CS08 (2015)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Airborne gravity data for CS08 collected in 2006 over 1 survey. This data set is part of the Gravity for the Re-definition of the American Vertical Datum (GRAV-D)...

  4. Medical aspects of 137Cs decorporation: The Goiania radiological accident

    International Nuclear Information System (INIS)

    Farina, R.; Brandao-Mello, C.E.; Oliveira, A.R.

    1991-01-01

    In September 1987, the Goiania radiological accident involving a source of 137 Cs culminated in about 140 victims who presented internal and/or external contamination and/or external exposure to radiation and/or radiation burns. Internal contamination was verified through analysis of urine and fecal samples. Internal contamination was also evaluated by measurements performed at the whole-body counter installed in Goiania in November 1987. To enhance the decorporation of 137Cs, patients were treated with the following: (1) Prussian Blue, oral administration, in 46 patients; (2) diuretics, oral administration, in 17 patients; (3) induced perspiration, increasing 137 Cs elimination. These procedures were done under rigorous clinical evaluation and considering the data from assay of excreta and data obtained from the whole-body counter. The doses of Prussian Blue exceeded about 6.5 times the dose previously indicated in the literature. It was the first time diuretics were used in humans to treat 137 Cs internal contamination. The results of these procedures are discussed

  5. Attenuation of trace organic compounds (TOrCs) inbioelectrochemical systems

    KAUST Repository

    Werner, Craig M.; Hoppe-Jones, Christiane; Saikaly, Pascal; Logan, Bruce E.; Amy, Gary L.

    2015-01-01

    , but no consistent trend could be identified regarding the physico-chemical properties of the TOrCs tested and the extent of sorption. The octanol-water distribution coefficient at pH 7.4 (log DpH 7.4) appeared to be a reasonable predictor for sorption of some

  6. Composite germanium monochromators - results for the TriCS

    Energy Technology Data Exchange (ETDEWEB)

    Schefer, J.; Fischer, S.; Boehm, M.; Keller, L.; Horisberger, M.; Medarde, M.; Fischer, P. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1997-09-01

    Composite germanium monochromators are in the beginning of their application in neutron diffraction. We show here the importance of the permanent quality control with neutrons on the example of the 311 wafers which will be used on the single crystal diffractometer TriCS at SINQ. (author) 2 figs., 3 refs.

  7. Synthesis and structural characterization of CsNiP crystal

    Indian Academy of Sciences (India)

    Unknown

    The crystals obtained by this method were of good quality exhibiting ... type framework structure having Cs atoms inside it (figures. 3 and 4). This helps for .... Gopalakrishna G S, Prasad J S and Lokanath N K 2001 Proc. joint 4th and 6th ICSTR ...

  8. Determination of the radioactive concentration of 137Cs in water

    International Nuclear Information System (INIS)

    1986-01-01

    The recently accepted standard method to determine the radioactive concentration of 137 Cs in water is based on the selective retention of cesium ions on ammonium-phosphorous-molybdate followed by the dissolution of the sorbent and the selective precipitation of cesium-hexa-chloro-platinate. The radioactive concentration is determined by the measurement of β disintegration rate of the preparate. (V.N.)

  9. Cs-137 in Norwegian Lapps in the spring of 1979

    International Nuclear Information System (INIS)

    Westerlund, E.A.; Jellum, W.; Arneberg, P.

    Measurements show that the body burden of Cs-137 in Lapps from Kautokeino diminished from 1965 to 1975 with an apparent half-life of 4-5 years. Since 1975 the reduction has been much slower. The Cs-137 content in reindeer meat has since 1966 diminished at the same rate. The reason for the lower rate of reduction since 1975 is that the fallout has received a contribution of Cs-137 from recent Chinese nuclear tests. The ratio of the average body burden of the Lapps who herd reindeer to the amount of Cs-137 in reindeer meat is 11.7 for men and 6.6 for women. The ratios for other Lapps are 8.1 and 4.7. Investigation of the seasonal variation of the body burden shows that measurements made at the end of March and beginning of April give values from which the annual dose may be calculated. The average dose from recent measurements for reindeer herders is about 25 mrad/year and about 2/3 of this for others. The Sr-90 measurements in reindeer bones are not related to health effects for the Lapps, but show how this parameter varies with time and indicates the environmental contamination by this nuclide. (JIW)

  10. Fallout 137Cs in reindeer herders in Arctic Norway.

    Science.gov (United States)

    Skuterud, Lavrans; Thørring, Håvard

    2015-03-03

    Reindeer herders in the Arctic were among the most heavily exposed populations to the global fallout from nuclear weapons testing in the 1950s and 1960s, due to high transfer of radionuclides in the lichens-reindeer-human food chain. Annual studies of (137)Cs in reindeer herders in Kautokeino, Norway, were initiated in 1965 to monitor radiation doses and follow environmental (137)Cs behavior. The (137)Cs concentrations declined from the peak in 1965 with effective half-times of 6-8 years, only interrupted by a temporary doubling in levels from 1986 to 1987 due to the Chernobyl fallout. During the period of 1950-2010 an average herder received an integrated effective dose from incorporated (137)Cs of about 18 mSv. This dose represents an insignificant increase in the risk for developing cancer. Health studies even show a significantly lower cancer incidence among Sámis and reindeer herders in northern Norway compared to other populations in the same area.

  11. Radioactivity precipitation Sr-90 and Cs-137 in Plock

    International Nuclear Information System (INIS)

    Flakiewicz, W.; Majkowska, I.; Bonkowski, J.

    1986-01-01

    Methods of research and results for beta-activity measurements of precipitation in 1977-1983 with regard to Sr-90, Cs-137 - are presented. Climatic changes caused by big industrial plant, conditions of pollution propagation in atmosphere, parameters of pollution load of Plock region are described. 11 refs., 6 figs., 5 tabs. (author)

  12. Sorption of Cs-137 and Co-60 in Natural Zeolites

    International Nuclear Information System (INIS)

    Chales Suarez, G.; Moreno Alvarez, D.; Coutin Correa, D.

    1996-01-01

    The sorption of Cs-137 and Co-60 in natural zeolites under different conditions was studied. The behaviour of samples of mineral and rock from different deposit of the country was obtained and the decontamination of radioactive waters containing both radionuclides was performed; as part of the research to determine its application in the treatment of radioactive wastes in the country

  13. Observation of high spin levels in Cs from Ba decay

    Indian Academy of Sciences (India)

    physics pp. 1157–1162. Observation of high spin levels in. 131. Cs from. 131. Ba decay. M SAINATH, DWARAKA RANI RAO*, K VENKATARAMANIAH and P C SOOD. Department of Physics, Sri Sathya Sai Institute of Higher Learning, Prasanthinilayam 515 134, India. £Permanent address: Department of Physics, ...

  14. Cs+ ion source for secondary ion mass spectrometry

    International Nuclear Information System (INIS)

    Bentz, B.L.; Weiss, H.; Liebl, H.

    1981-12-01

    Various types of cesium ionization sources currently used in secondary ion mass spectrometry are briefly reviewed, followed by a description of the design and performance of a novel, thermal surface ionization Cs + source developed in this laboratory. The source was evaluated for secondary ion mass spectrometry applications using the COALA ion microprobe mass analyzer. (orig.)

  15. Cs0.49NbPS6

    Directory of Open Access Journals (Sweden)

    Hoseop Yun

    2011-01-01

    Full Text Available The quaternary thiophosphate, Cs0.49NbPS6, caesium hexathioniobiophosphate(V, has been synthesized by the reactive halide flux method. The title compound is isotypic with Rb0.46TaPS6 and is made up of a bicapped trigonal–biprismatic [Nb2S12] unit and a tetrahedral [PS4] group. The [Nb2S12] units linked by the [PS4] tetrahedra form infinite chains, yielding a three-dimensional network with rather large van der Waals gaps along the c axis in which the disordered Cs+ ions reside. The electrons released by the Cs atoms are transferred to the pairwise niobium metal site and there are substantial intermetallic Nb—Nb bonding interactions. This leads to a significant decrease of the intermetallic distance in the title compound compared to that in TaPS6. The classical charge balance of the title compound may be represented as [Cs+]0.49[Nb4.51+][P5+][S2−]4[S22−].

  16. 90Sr and 137Cs content in fishes

    International Nuclear Information System (INIS)

    Patin, S.A.; Petrov, A.A.

    1978-01-01

    Numerous data are presented and discussed on concentrations of 90 Sr in bones and 137 Cs in muscular tissues of main food fishes fished out in different regions of the ocean, seas, lakes and rivers. They are indicative of the absence of appreciable hygienic hazards for man from eating food fishes

  17. Distribuição de 137Cs em três solos representativos do estado de pernambuco Distribution of 137Cs in three representative soils of pernambuco state, Brazil

    Directory of Open Access Journals (Sweden)

    Patrik Diogo Antunes

    2010-06-01

    Full Text Available O 137Cs tem sido usado para quantificar perdas ou deposição de solo, com base em valores das concentrações em áreas de referência que tiveram pouca perturbação nas últimas décadas. Determinações em áreas assim ainda não foram feitas na região Nordeste do Brasil. Em Pernambuco, foram selecionadas três áreas com topografia plana, vegetação nativa e solos não perturbados, em Goiana, Sertânia e Araripina. Em cada área, foram marcados quatro pontos, distantes 20 a 50 m um do outro, e em cada um retiradas amostras de solo, em camadas consecutivas de 3 cm de espessura, até 30 cm. As atividades de 137Cs foram determinadas usando espectrometria gama com detector de germânio hiperpuro (HPGe. Os estoques médios de 137Cs (Bq m-2 foram de 71,6 ± 6,3 em Goiana, 64,0 ± 13,8 em Araripina e 95,5 ± 9,8 em Sertânia. Valores nessa faixa têm sido relatados na Paraíba e na Bahia e, mais altos, na região Sudeste, confirmando a diminuição dos estoques em áreas mais próximas do Equador. As maiores atividades ocorreram nas camadas superficiais, variando de 0,5 a 1,6 Bq kg-1, e decresceram linearmente com a profundidade, até os limites de detecção: 18 cm em Araripina, 15 cm em Goiana e 9 cm em Sertânia. Em Goiana, acima dos horizontes inorgânicos havia um horizonte orgânico, com a mais alta atividade (2,06 Bq kg-1. Atividades e estoque altos e menor aprofundamento em Sertânia poderiam ser explicados pela predominância de argilominerais 2:1, em contraposição à de argilominerais 1:1 nos outros locais. Houve correlações positivas entre a atividade de 137Cs e os valores de pH em água e KCl e correlação negativa com as concentrações de Al3+. Confirma-se que, em áreas de referência, a maior atividade do 137Cs está na camada superior, com decréscimos regulares ao longo do perfil do solo.Contents of 137Cs have been used to quantify soil loss or accumulations, based on values of reference sites with little soil disturbance

  18. Knudsen cell mass spectrometric study of the Cs2IOH(g) molecule thermodynamics

    International Nuclear Information System (INIS)

    Roki, F-Z.; Ohnet, M-N.; Fillet, S.; Chatillon, C.; Nuta, I.

    2013-01-01

    Highlights: • The pronounced ionic character leads to only dissociative ionization processes. • Ions formed are same as those coming from pure dimmers. • De-convolution of the ions origin needs accurate thermodynamic values for the pure gas phase. • Mass spectrometric interpretation has to be performed gradually and as a function of suitable condensed compositions. • Thermal functions have to be fully estimated. -- Abstract: The gas phase of the CsI + CsOH system is analyzed by high temperature Knudsen cell mass spectrometry in order to confirm the existence of the Cs 2 IOH(g) complex molecule. The mass spectrometric analysis is quite complex since such molecules undergo dissociative ionization into fragment ions that mix with the same ions from dimers of the pure compounds in the same vapor phase. Varying the chemical conditions for vaporization by using different CsI + CsOH mixture contents showed that the ionization of the Cs 2 IOH(g) molecule led to five different fragment ions, Cs 2 OH + , Cs 2 I + , Cs + , CsOH + and CsI + . This complex ionization pattern was studied in relation with previous assessed values for the vaporization of CsOH and CsI pure compounds in which monomer and dimer molecules are predominant. The equilibrium constant for the reaction CsI(g) + CsOH(g) = Cs 2 IOH(g) was determined and, after modeling the structure of the Cs 2 IOH molecule, the enthalpy of formation was determined using the third law of thermodynamics, as follows: Δ f H°(Cs 2 IOH, g, 298.15 K) = −578 ± 14.7 kJ · mole −1

  19. Determination of migration speed and the partition ratios of 137 Cs in the soils of the future waste repository in Abadia de Goias, GO, Brazil

    International Nuclear Information System (INIS)

    Pereira, Jose Carlos Alves

    1996-01-01

    The dispersion of a 51 TBq 137 Cs source to the environment in Goiania city, has originated approximately 3500 m 3 of radioactive waste. In order to segregate such waste in a definite form, a repository is being built in Abadia de Goias, GO near the site where it has been temporarily stored. This study had the following objectives: the determination of the 137 Cs partition rate (K D ) and the estimate of its migration velocity in soil samples from the site where the repository is being built. The determination of 137 Cs K D was carried out by using two methods: 'batch method' and 'in-situ' method. In relation to the 'batch method'; 6 soil profiles cut into sections according to its pedologic horizons and 13 surface soil samples were collected, whereas for the 'in-situ' method 6 soil profiles with 28 cm depth were collected and each profile has been cut into 14 soil sections of a 1-3 cm range. Studies were carried out by using the 'batch method' to relate the influence from v/m and from shaking in K D determination and also studies about 137 Cs adsorption reversibility in soil, time necessary for the equilibrium of 137 Cs between water/soil phases to be reached and K D correlation with pedological parameters (pH values in water and clay, silt and organic material percent concentration, electrical conductivity of solution and the cation exchange - Ca +2 , Mg +2 , K +2 , Na + , Al +3 , H + ). It has been noticed that in work conditions, K D has increased according to the rate increase v/m and the use of agitation in water/soil phases had no influence in K D determination. The absorbed 137 Cs desorption process by water has shown to be slow but continued. Nevertheless, 137 Cs cationic exchange for NH 4 + has presented two steps: the first one very fast where approximately 50% of 137 Cs adsorbed has been exchanged for NH 4 + ions in just two days and the second one slow. Results indicate that 137 Cs adsorption process in this kind of soil may be considered reversible

  20. Near-Ultraviolet Observations of CS 29497-030: New Constraints on Neutron-Capture Nucleosynthesis Processes

    Science.gov (United States)

    Ivans, Inese I.; Sneden, Christopher; Gallino, Roberto; Cowan, John J.; Preston, George W.

    2005-07-01

    Employing spectra obtained with the new Keck I HIRES near-UV-sensitive detector, we have performed a comprehensive chemical composition analysis of the binary blue metal-poor star CS 29497-030. Abundances for 29 elements and upper limits for an additional seven have been derived, concentrating on elements largely produced by means of neutron-capture nucleosynthesis. Included in our analysis are the two elements that define the termination point of the slow neutron-capture process, lead and bismuth. We determine an extremely high value of [Pb/Fe]=+3.65+/-0.07 (σ=0.13) from three features, supporting the single-feature result obtained in previous studies. We detect Bi for the first time in a metal-poor star. Our derived Bi/Pb ratio is in accord with those predicted from the most recent FRANEC calculations of the slow neutron-capture process in low-mass asymptotic giant branch (AGB) stars. We find that the neutron-capture elemental abundances of CS 29497-030 are best explained by an AGB model that also includes very significant amounts of pre-enrichment of rapid neutron-capture process material in the protostellar cloud out of which the CS 29497-030 binary system formed. Mass transfer is consistent with the observed [Nb/Zr]~0. Thus, CS 29497-030 is both an r+s and ``extrinsic AGB'' star. Furthermore, we find that the mass of the AGB model can be further constrained by the abundance of the light odd-element Na. The data presented herein were obtained at the W. M. Keck Observatory, which is operated as a scientific partnership among the California Institute of Technology, the University of California, and NASA. The Observatory was made possible by the generous financial support of the W. M. Keck Foundation.