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Sample records for cadmium iodide crystals

  1. Observation of crystallization and characterizations on thiourea cadmium iodide: A semi-organic optical material

    Energy Technology Data Exchange (ETDEWEB)

    Singh, Preeti; Hasmuddin, Mohd. [Crystal Growth and XRD Lab, Department of Physics, Jamia Millia Islamia, New Delhi 110025 (India); Abdullah, M.M. [Crystal Growth and XRD Lab, Department of Physics, Jamia Millia Islamia, New Delhi 110025 (India); Promising Centre for Sensors and Electronic Devices (PCSED), Department of Physics, Faculty of Sciences and Arts, Najran University, P.O. Box 1988, Najran 11001 (Saudi Arabia); Shkir, Mohd. [Crystal Growth and XRD Lab, Department of Physics, Jamia Millia Islamia, New Delhi 110025 (India) and Department of Physics, ARSD College, University of Delhi, New Delhi 110021 (India); Wahab, M.A., E-mail: aries.pre84@gmail.com [Crystal Growth and XRD Lab, Department of Physics, Jamia Millia Islamia, New Delhi 110025 (India)

    2013-10-15

    Graphical abstract: - Highlights: • Thiourea cadmium iodide (TCI) was grown by slow evaporation solution technique. • Morphology and growth rate of the grown compound are determined with the help of inverted microscope. • Optical band gap has been determined. • Microstructure analysis has been reported. • Electrical study has been reported and discussed. - Abstract: In this work, the single crystals of thiourea cadmium iodide were grown by slow evaporation solution technique in two different ratios 2:1 and 1:1. During the formation of their single crystals the morphological features and its live growth process were recorded with the help of inverted microscope. Structural studies of the grown crystals have been carried out by powder X-ray diffraction to confirm the crystal system and vibrational modes by Raman spectroscopy. The optical energy band gaps were investigated through UV–vis spectroscopy study. The surface morphology of the grown single crystals was analyzed by using Scanning Electron Microscope and thermal analysis was carried out by using thermogravimetric analysis. The electrical properties were also studied as a function of frequency and the obtained results are discussed.

  2. Synthesis, crystal growth and characterizations of bis ( l-proline) cadmium iodide: a new semi-organic nonlinear optical material

    Science.gov (United States)

    Boopathi, K.; Jagan, R.; Ramasamy, P.

    2016-07-01

    Novel semi-organic single crystals of bis ( l-proline) cadmium iodide (BLPC) were grown by slow evaporation technique. The crystal structure was determined by single-crystal X-ray diffraction studies. Single-crystal X-ray diffraction study shows that [BLPC] crystallizes in orthorhombic system with space group P212121. 1H NMR and 13C NMR studies were conducted for the grown crystal. Functional groups present in the compound were identified by FTIR spectral studies. The UV-Vis-NIR spectrum was studied to analyse the optical properties of the grown crystals. Thermogravimetric analysis was carried out to study thermal behaviour of the materials. Vickers microhardness measurement was carried out for different loads. Etching studies were carried out using water as etchant. The second harmonic generation efficiency was determined by the Kurtz powder method and it was found to be higher than that of potassium dihydrogen phosphate.

  3. A combined optical, SEM and STM study of growth spirals on the polytypic cadmium iodide crystals

    Indian Academy of Sciences (India)

    Rajendra Singh; S B Samanta; A V Narlikar; G C Trigunayat

    2000-04-01

    Some novel results of a combined sequential study of growth spirals on the basal surface of the richly polytypic CdI2 crystals by optical microscopy, scanning electron microscopy (SEM) and scanning tunneling microscopy (STM) are presented and discussed. In confirmation of the known structural data, the STM pictures clearly reveal the value of unit cell (=) dimension to be equal to 0.428 nm and the value of the interaxial angle to be equal to 120°. Under the high resolution and magnification achieved in the scanning electron microscope, the growth steps of large heights seen in the optical micrographs are found to have a large number of additional steps of smaller heights existing between any two adjacent large height growth steps. When further seen by a scanning tunneling microscope, which provides still higher resolution, several unit substeps are seen to exist between two consecutive additional steps. The height of each substep is found to be equal to the unit cell height of the underlying polytype. The height of the larger additional steps are found to be integral multiple of the unit cell height. The horizontal distance between two consecutive growth steps is found to be an integral multiple of the lattice parameter . The interspacing of the growth steps of same step height is found to vary at different positions on the same crystal face.

  4. Synthesis and Structure of Bis(4-nitrobenzaldehyde thiosemicarbazone) Cadmium Iodide

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    The title complex, bis(4-nitrobenzaldehyde thiosemicarbazone) cadmium iodide (C16H16CdI2N8O4S2) crystallizes in the triclinic system, space group P1 with a=9.632(2), b=11.227(2), c=14.031(3), α= 67.50(3), β= 86.99(3), γ= 66.64(3)°, V=1278.13, Z = 2, Dc = 2.117gcm-3, F(000) = 772, μ =3.472mm-1 MoKα radiation (λ=0.71073), R = 0.0443, wR= 0.1425 for 4529 observed reflections [I>2σ(I)] of 4731 independent reflections. The result shows that the structure contains CdL2I2 (where L = 4-nitrobenzaldehyde thiosemicarbazone) distorted tetrahedral units in which the two ligands are S-bonded as monodentate to cadmium ion; the two iodide ions are also coordinated to Cd(II).

  5. Processes of adsorption/desorption of iodides and cadmium cations onto/from Ag(111

    Directory of Open Access Journals (Sweden)

    VLADIMIR D. JOVIĆ

    2011-02-01

    Full Text Available In this work, the adsorption/desorption processes of iodides and cadmium cations in the presence of iodides onto/from Ag(111 were investigated. It was shown that both processes were complex, characterized by several peaks on the cyclic voltammograms (CVs. By PeakFit analysis of the recorded CVs and subsequent fitting of the obtained peaks by the Frumkin adsorption isotherm, the interaction parameter (f and the Gibbs energy of adsorption (DGads for each adsorbed phase were determined. In the case of iodide adsorption, four peaks were characterized by negative values of f, indicating attractive lateral interaction between the adsorbed anions, while two of them possessed value of f < –4, indicating phase transition processes. The adsorption/desorption processes of cadmium cations (underpotential deposition – UPD of cadmium in the presence of iodide anions was characterized by two main peaks, each of them being composed of two or three peaks with negative values of f. By the analysis of charge vs. potential dependences obtained either from the CVs or current transients on potentiostatic pulses, it was concluded that adsorbed iodides did not undergo desorption during the process of Cd UPD, but became replaced by Cd ad-atoms and remained adsorbed on top of a Cd layer and/or in between Cd the ad-atoms.

  6. Theoretical calculations of primary particle condensation for cadmium and caesium iodide vapours

    International Nuclear Information System (INIS)

    This report considers a model of aerosol nucleation from the vapour phase which has been developed by Buckle. The applicability of the model has been tested by considering the condensation of caesium iodide and cadmium vapours under a wide variety of pre-mixed flow conditions of interest to PWR severe accident studies. (U.K.)

  7. Mercuric iodide crystals obtained by solvent evaporation using ethanol

    International Nuclear Information System (INIS)

    Millimeter-sized mercuric iodide crystals were fabricated by the solvent evaporation technique using pure ethanol as a solvent. Three different conditions for solution evaporation were tested: (i) in the dark at room temperature; (ii) in the presence of light at room temperature and (iii) in an oven at 40 deg. C. Morphology, structure, optical and electrical properties were investigated using several techniques. Crystals fabricated in the dark show better properties and stability than others, possibly because the larger the energy of the system, the larger the number of induced growth defects. The crystals fabricated in the dark have adequate structure for higher resistivity and activation energy close to half the optical band-gap, as desired. With proper encapsulation these crystals might be good candidates for the development of ionizing radiation sensors.

  8. Synthesis, growth, structural, thermal, optical properties of new metal-organic crystals: Methyltriphenylphosphonium iodide thiourea and methyltriphenylphosphonium iodide chloroform hemisolvate

    Science.gov (United States)

    Shivachev, Boris L.; Kossev, Krassimir; Dimowa, Louiza T.; Yankov, Georgi; Petrov, Todor; Nikolova, Rositsa P.; Petrova, Nadia

    2013-08-01

    Crystals of methyltriphenylphosphonium iodide thiourea (1) and methyltriphenylphosphonium iodide chloroform hemisolvate (2) were obtained for the first time. Fourier transform infrared (FTIR) spectral studies have been performed to identify the functional groups. Thermogravimetric analysis (TGA) and differential thermal analysis (DTA) were used to study their thermal properties. The optical transmittance window and the lower cutoff wavelength have been identified by UV-vis studies. Crystals of the title compounds suitable for single crystal X-ray analyses were successfully grown by slow evaporation and diffraction data were collected to elucidate the molecular structure and interactions. The proton donors (phosphonium) and proton acceptor (iodine) in the structure of 1 provide infrastructure to introduce charge asymmetry while in 2 chloroform molecule is not involved in the charge transfer. An optical quality crystal of 1 (5×4×2 mm3) was obtained by macroseeding. The crystal has developed facets with major ones (001) and (00¯1). A crystal of 1 was tested with 1060 nm laser radiation and showed second harmonic generation (SHG).

  9. Thermogravimetric and calorimetric study of cadmium iodide adducts with cyclic ureas

    International Nuclear Information System (INIS)

    Adducts of general formula CdI2·nL [n=1 and 2; L: ethyleneurea (eu) and propyleneurea (pu)] were synthesized by a solid state route and characterized by elemental analysis, infrared spectroscopy, thermogravimetry and reaction solution calorimetry. The infrared results shown that eu and pu coordinate through oxygen atom. All adducts release the ligand molecules in a single mass loss step, suggesting that, in the bisadducts, both ligand molecules are in equivalent coordination sites, exhibiting similar bond enthalpies. For all thermogravimetric curves, the first mass loss step is associated with the release of ligand molecules and the second one with the sublimation of cadmium iodide: CdI2·nL(s)→CdI2(s)+nL(g); CdI2(s)→CdI2(g). The observed thermal stability trend is: CdI2·eu (228 deg. C) > CdI2·pu (213 deg. C) > CdI2·2pu (200) > CdI2·2eu (186 deg. C). The standard molar reaction enthalpy in condensed phase: CdI2(cr)+nL(cr)=CdI2·nL(cr); ΔrHmθ, were obtained from reaction-solution calorimetry, to give the following values for mono and bisadducts: -7.16 and -27.61, -4.99 and -9.07 kJ mol-1 for eu and pu adducts, respectively. Decomposition (ΔDHmθ) and lattice (ΔMHmθ) enthalpies, as well as the mean cadmium-oxygen bond dissociation enthalpy, D(Cd-O), were calculated for all adducts

  10. Doping in mercuric iodide crystals and its influence on electronic properties and material structure

    International Nuclear Information System (INIS)

    Doping of mercuric iodide single crystals with SbI3 was studied. Three major aspects of the influence of doping were investigated: the α to β solid phase transition, the crystal structure and the semiconducting properties. A controlled doping method and a new growth technique from the melt were developed. A quantitative correlation between the antimony concentration and the charge carrier transport properties as well as the nuclear detector characteristics of HgI2 were established for the first time. In the present work the influence of various impurities (Sb, Cu, Ag, Bi) on the solid state phase transformation of mercuric iodide has been investigated. In the second part of the work a new growth method for mercuric iodide single crystals containing a controlled amount of SbI3, has been developed. In the last part of this work the influence of the presence of impurities in the crystal on the charge carrier transport properties has been investigated. (author)

  11. Barium iodide and strontium iodide crystals and scintillators implementing the same

    Energy Technology Data Exchange (ETDEWEB)

    Payne, Stephen A.; Cherepy, Nerine; Pedrini, Christian; Burger, Arnold

    2016-09-13

    In one embodiment, a crystal includes at least one metal halide; and an activator dopant comprising ytterbium. In another general embodiment, a scintillator optic includes: at least one metal halide doped with a plurality of activators, the plurality of activators comprising: a first activator comprising europium, and a second activator comprising ytterbium. In yet another general embodiment, a method for manufacturing a crystal suitable for use in a scintillator includes mixing one or more salts with a source of at least one dopant activator comprising ytterbium; heating the mixture above a melting point of the salt(s); and cooling the heated mixture to a temperature below the melting point of the salts. Additional materials, systems, and methods are presented.

  12. Spectrophotometric determination of trace amount of cadmium with iodide and methyl violet

    International Nuclear Information System (INIS)

    A selective spectrophotometric method based on the interaction of an anionic iodo complex of cadmium with methyl violet has been described for the determination of trace amounts of cadmium. The developed method is precise, accurate and has been applied to determination of cadmium at trace levels (25 ppb) in sea water and high purity sample of indium and zinc materials. (author). 10 refs., 2 tabs

  13. Furnace design for the mercuric iodide crystal growth for new semiconductor radiation detector

    International Nuclear Information System (INIS)

    Mercuric iodide has been attracted an interest for 40 years due to its efficiency as room temperature detector for X and γ-rays. It is worthy to note that commercial γ-ray detectors such as Ge semiconductor detectors should cool down to liquid nitrogen temperature. Compared to other semiconductor detectors such as CdZnTe and CdTe, mercuric iodide has higher efficiency, lower leakage current and less degradation. In addition, mercuric iodide has useful properties such as large band gap of 2.15 eV, low electron-hole pair creation energy of 4.2 eV, and high atomic number (Hg : 80 and I : 53). However, it is difficult to obtain high quality single crystals and the long term reliability problem in devices so that the applications of α-HgI2 are limited. Mercuric iodide undergoes a structural phase transition from an orthorhombic yellow phase (β-HgI2) to a tetragonal red phase (α-HgI2) at 127 .deg. C. In addition, the melting temperature of HgI2 is 259 .deg. C. Thus, when it grows through a melting method over 259 .deg. C, the β-HgI2 phase can be included in the final crystals in the room temperature. In general, in order to grow α-HgI2single crystals, the operating temperature is below 127 .deg. C. Note that the crystals from the solution method have contamination problems and the crystals from the physical vapor method usually display a higher quality with a well defined structure. A good thing for the physical vapor method is that α-HgI2 has high vapor pressure (∼0.1 Torr at 120 .deg. C) indicating that α-HgI2 can be grown in closed ampoules

  14. Luminescence properties of crystals of lead iodides with manganese addition

    International Nuclear Information System (INIS)

    The luminescence properties of the Pbl2 and Pbl2 : 0.5 mol MnCl2 crystals by excitation through the X-ray beams and N2-laser light are studied within the temperature range of 85-295 K. Bands with the maxima about 495 and 512 nm were observed in the Pbl2 photoluminescence spectra at 85 K. The roentgenoluminescence spectra at this temperature are represented by the bands of 515 and 715 nm. Introduction of the manganese addition into the Pbl2 leads to decrease in the intensity of the short-wave bands and increase in the intensity of the long-wave band and displacement of its maximum up to 700 nm. Increase in the crystals temperature from 85 up to 295 K results in the luminescence quenching. At the room temperature the Pbl2 : Mn roentgenoluminescence yield with the maximum of 660 nm is approximately by three times higher than the Pbl2 roentgenoluminescence yield with the maximum of 555 nm. The nature of the luminescence bands and mechanisms of the radiation processes in the studied crystals are discussed

  15. Cosmic muon tomography of pure cesium iodide calorimeter crystals

    CERN Document Server

    Frlez, E; Assamagan, Ketevi A; Brönnimann, C; Flügel, T; Krause, B; Lawrence, D W; Mzhavia, D A; Pocanic, D; Renker, D; Ritt, S; Slocum, P L; Soic, N; Br"onnimann, Ch.; Fl"ugel, Th.

    2000-01-01

    Scintillation properties of pure CsI crystals used in the shower calorimeter being built for precise determination of the pi+ -> pi0 e+ nu decay rate are reported. Seventy-four individual crystals, polished and wrapped in Teflon foil, were examined in a multiwire drift chamber system specially designed for transmission cosmic muon tomography. Critical elements of the apparatus and reconstruction algorithms enabling measurement of spatial detector optical nonuniformities are described. Results are compared with a Monte Carlo simulation of the light response of an ideal detector. The deduced optical nonuniformity contributions to the FWHM energy resolution of the PIBETA CsI calorimeter for the pi+ -> e+ nu 69.8 MeV positrons and the monoenergetic 70.8 MeV photons were 2.7% and 3.7%, respectively. The upper limit of optical nonuniformity correction to the 69.8 MeV positron low-energy tail between 5 MeV and 55 MeV was +0.2%, as opposed to the +0.3% tail contribution for the photon of the equivalent total energy. ...

  16. High-Performance Doped Strontium Iodide Crystal Growth Using a Modified Bridgman Method

    Science.gov (United States)

    Rowe, Emmanuel

    dipole-allowed and thus are about 106 times stronger than the more frequently observed 4f-4f transition in the trivalent rare earth ions. Ce3+, Nd3+ and Pr3+ have been investigated for fast response applications while Ce3+, Eu 2+, and Yb2+ stand out as the most promising activators offering high light yield, and high energy resolution. Using a modified Bridgman growth technique we have grown crystals with a low energy resolution of 2.6% at 662 keV, which is lower than the previous 2.8% reported for SrI2:Eu 2+. The modified technique (called so for its vertical crystal growth orientation) is necessary due to the anisotropic thermal expansion coefficient of Strontium Iodide. The problem plaguing the growth of the crystal is spontaneous cracking, which usually appear during cooling in the bulk. With the use of a zone separating shield, one can achieve more control of the temperature gradient between the two zones without compromising the actual temperature of the two zones. Additionally the use of codopants, in particular divalent magnesium improved the crystalline quality by acting as a gathering for iodine ions, which led to reduction of defect density.

  17. Growth of cadmium oxide whiskers on cadmium sulphide single crystals with copper as growth activator

    Energy Technology Data Exchange (ETDEWEB)

    Koparanova, N.; Simov, S. (Bylgarska Akademiya na Naukite, Sofia. Inst. po Fizika na Tvyrdoto Tyalo); Genchev, D. (Bylgarska Akademiya na Naukite, Sofia. Inst. za Yadrena Izsledvaniya i Yadrena Energetika); Metchenov, G. (Research Inst. of Criminalistics and Criminology, Sofia (Bulgaria))

    1985-02-01

    Some results on the growth and morphology of cadmium oxide whiskers, obtained on cadmium sulphide single crystals with copper as a growth activator, are presented in this work. Cadmium oxide whiskers have been obtained on brace 112-bar0 brace faces of cadmium sulphide plates with a copper layer deposited in advance. The whiskers grew during the annealing of the plates in a weak stream of technically pure argon at temperatures 670 to 730 deg C for 15 min to 3.5 h. Details about the procedure have been given elsewhere. The composition and morphology of the whiskers have been studied by an X-ray microanalyser JEOL 35 DDS and a scanning electron microscope JEOL, JSM 35. The optical microscopic observations have shown that after annealing, a gray-black granular layer is formed on the cadmium sulphide single crystals and this layer can easily be separated from the crystal substrate. Under the granular layer the crystal is heavily damaged. The whiskers grow on the granular layer and they are coloured yellow-brown or red-brown. The maximum whisker length attains several hundreds of micrometres and in some cases up to 1 mm or more.

  18. Inclusion free cadmium zinc tellurium and cadmium tellurium crystals and associated growth method

    Science.gov (United States)

    Bolotnikov, Aleskey E.; James, Ralph B.

    2010-07-20

    The present disclosure provides systems and methods for crystal growth of cadmium zinc tellurium (CZT) and cadmium tellurium (CdTe) crystals with an inverted growth reactor chamber. The inverted growth reactor chamber enables growth of single, large, high purity CZT and CdTe crystals that can be used, for example, in X-ray and gamma detection, substrates for infrared detectors, or the like. The inverted growth reactor chamber enables reductions in the presence of Te inclusions, which are recognized as an important limiting factor in using CZT or CdTe as radiation detectors. The inverted growth reactor chamber can be utilized with existing crystal growth techniques such as the Bridgman crystal growth mechanism and the like. In an exemplary embodiment, the inverted growth reactor chamber is a U-shaped ampoule.

  19. Growth of single crystals of mercuric iodide (HgI2) in spacelab III

    International Nuclear Information System (INIS)

    Continued development of a system designed to grow crystals by physical vapor transport in the environment of Spacelab III will be described, with special emphasis on simulation of expected space conditions, adjustment of crystal growth parameters, and on board observation and control of the experiment by crew members and ground personnel. A critical factor in the use of mercuric iodide for semiconductor detectors of x-rays and gamma-rays is the crystalline quality of the material. The twofold purpose of the Spacelab III experiment is therefore to grow single crystals with superior electronic properties as an indirect result of the greatly reduced gravity field during the growth, and to obtain data which will lead to improved understanding of the vapor transport mechanism. The experiments planned to evaluate the space crystals, including gamma-ray diffractometry and measurements of stoichiometry, lattice dimensions, mechanical strength, luminescense, and detector performance are discussed

  20. Spectrophotometric determination of trace amounts of cadmium and lead with iodide and rhodamine B

    International Nuclear Information System (INIS)

    Highly sensitive spectrophotometric methods have been developed for determination of cadmium and lead, based on the CdI42- or PbI42- anionic complexes with Rhodamine B in the presence of polyvinyl alcohol to form ion-association complexes. The molar absorptivity is 4.2x105 l x mole-1 x cm-1 at 600 nm for cadmium and 5.7x105 l x mole-1 x cm-1 at 610 nm for lead. The complexes have the composition [CdI 42-] x [RhB+]2 and [PbI42-] x [RhB+]2 as established by Job's method of continuous variations and the molar-ratio method. The colour reaction selectivity is fairly good and the method can be applied for direct spectrophotometric determination of cadmium or lead in some pure metals. A species [PbI3-] x [RhB+] can also be formed, and extracted into toluene or a toluene/diethyl ether micture. (Authors)

  1. Structural and mechanical studies of cadmium manganese thiocyanate crystal

    Science.gov (United States)

    Manikandan, M. R.; Vijayaprasath, G.; babu, G. Anandha; Bhagavannarayan, G.; Vijayan, N.; Ravi, G.

    2012-06-01

    Single crystals of cadmium manganese thiocyanate (CMTC) have been synthesized successfully and grown by slow evaporation method. The structural perfection of the grown crystals has been analyzed by High resolution X-ray diffraction (HRXRD), which shows the crystalline perfection of the grown crystal is quite good. Optical behavior was assessed by UV-Vis analysis and found that no absorption in the UV visible region and it may be useful for second harmonic applications. The mechanical hardness of the grown crystals was studied and Vicker's microhardness, Stiffness constant was calculated.

  2. Growth and characterization of cadmium magnesium tetra thiocyanate crystals

    Energy Technology Data Exchange (ETDEWEB)

    Gunasekaran, S. [Post Graduate and Research Department of Physics, Pachaiyappa' s College, Chennai - 600 030 (India); Ponnusamy, S. [Department of Physics, S. R. M. Institute of Science and Technology, Kattankulathur - 603 203 (India)

    2006-02-01

    Cadmium Magnesium Tetra Thiocyanate, CdMg(SCN){sub 4}, [CMTC] belongs to bimetallic thiocyanate complexes. CMTC crystals has been grown by solution growth technique at room temperature. The morphologies of the grown crystals are identified by single crystal analysis. Also the Powder X-ray Diffractogram of the crystal has been recorded and the various planes of reflection are identified. The title compound crystallizes under triclinic structure with lattice parameters a=10.0976 Aa, b=7.5015 Aa, c=5.7720 Aa and {beta}=90.2135 . The presence of magnesium and cadmium in the grown crystals were confirmed through Atomic Absorption Spectroscopy. The grown crystals are analysed qualitatively by Fourier Transform Infrared (FTIR) and Fourier Transform Raman spectral measurements. The transmittance spectrum of the crystal in the UV-Visible region has been recorded and analysed. The dielectric measurements for the crystals were carried out in the microwave region. The thermal stabilities of the crystals were studied by using different thermal analyses like Thermo Gravimetric Analysis (TGA), Differential Thermal Analysis (DTA) and Differential Scanning Calorimetry (DSC). (copyright 2006 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  3. Structural, spectral and mechanical studies of bimetallic crystal: cadmium manganese thiocyanate single crystals

    Science.gov (United States)

    Manikandan, M.; Vijaya Prasath, G.; Bhagavannarayan, G.; Vijayan, N.; Mahalingam, T.; Ravi, G.

    2012-09-01

    A nonlinear optical bimetallic thiocyanate complex crystal, cadmium manganese thiocyanate (CMTC) has been successfully synthesized. The growth of single crystals of cadmium manganese thiocyanate has been accomplished from aqueous solution using slow evaporation method. The presence of manganese and cadmium in the synthesized material was confirmed through energy dispersive spectrum (EDS) analysis. Structural analysis was carried out using powder X-ray diffractometer (PXRD) and crystalline perfection of the grown crystals was ascertained by high-resolution X-ray diffraction (HRXRD) analysis. Fourier transform infrared (FTIR) spectrum was taken to confirm the functional groups. The transmittance spectrum of the crystal in the UV-visible region has been recorded and the cutoff wavelength has been determined. The dielectric measurements for the crystals were performed for various frequencies and temperatures. The mechanical properties were evaluated by Vickers microhardness testing, which reveals hardness and stiffness constant of the crystals.

  4. Structural, spectral and mechanical studies of bimetallic crystal: cadmium manganese thiocyanate single crystals

    Energy Technology Data Exchange (ETDEWEB)

    Manikandan, M.; Vijaya Prasath, G.; Mahalingam, T.; Ravi, G. [Alagappa University, Department of Physics, Karaikudi (India); Bhagavannarayan, G.; Vijayan, N. [National Physical Laboratory, Materials Characterization Division, New Delhi (India)

    2012-09-15

    A nonlinear optical bimetallic thiocyanate complex crystal, cadmium manganese thiocyanate (CMTC) has been successfully synthesized. The growth of single crystals of cadmium manganese thiocyanate has been accomplished from aqueous solution using slow evaporation method. The presence of manganese and cadmium in the synthesized material was confirmed through energy dispersive spectrum (EDS) analysis. Structural analysis was carried out using powder X-ray diffractometer (PXRD) and crystalline perfection of the grown crystals was ascertained by high-resolution X-ray diffraction (HRXRD) analysis. Fourier transform infrared (FTIR) spectrum was taken to confirm the functional groups. The transmittance spectrum of the crystal in the UV-visible region has been recorded and the cutoff wavelength has been determined. The dielectric measurements for the crystals were performed for various frequencies and temperatures. The mechanical properties were evaluated by Vickers microhardness testing, which reveals hardness and stiffness constant of the crystals. (orig.)

  5. Growth and Characterization of Morpholium Cadmium Acetoperchlorate Single Crystal

    Directory of Open Access Journals (Sweden)

    D. Shyamala

    2016-06-01

    Full Text Available In the search for novel crystal with promising nonlinear optical properties an attempt is made to grow morpholium cadmium aceto-perchlorate single crystals. The title compound is synthesized by slow evaporation technique at room temperature. The powder X-ray diffraction pattern has been recorded and the various planes of reflections are identified. The transmittance spectrum of the crystal in the UV–Vis region has been obtained. Using the FTIR spectrum, the vibrational modes of the crystal is analysed and the presence of cadmium in the crystal is confirmed. Thermogravimetric analysis and differential thermal analysis studies have been done to assess the thermal stability of the grown crystal. The dielectric measurement for the crystal is carried out in the range of 50 Hz to 5 MHz for three different temperatures 40ºC, 80ºC and 120ºC to study the electrical nature of the grown crystal. The nonlinear optical property of the grown crystal is confirmed.

  6. Photoluminescence Blinking of Single-Crystal Methylammonium Lead Iodide Perovskite Nanorods Induced by Surface Traps

    Science.gov (United States)

    2016-01-01

    Photoluminescence (PL) of organometal halide perovskite materials reflects the charge dynamics inside of the material and thus contains important information for understanding the electro-optical properties of the material. Interpretation of PL blinking of methylammonium lead iodide (MAPbI3) nanostructures observed on polycrystalline samples remains puzzling owing to their intrinsic disordered nature. Here, we report a novel method for the synthesis of high-quality single-crystal MAPbI3 nanorods and demonstrate a single-crystal study on MAPbI3 PL blinking. At low excitation power densities, two-state blinking was found on individual nanorods with dimensions of several hundred nanometers. A super-resolution localization study on the blinking of individual nanorods showed that single crystals of several hundred nanometers emit and blink as a whole, without showing changes in the localization center over the crystal. Moreover, both the blinking ON and OFF times showed power-law distributions, indicating trapping–detrapping processes. This is further supported by the PL decay times of the individual nanorods, which were found to correlate with the ON/OFF states. Furthermore, a strong environmental dependence of the nanorod PL blinking was revealed by comparing the measurements in vacuum, nitrogen, and air, implying that traps locate close to crystal surfaces. We explain our observations by proposing surface charge traps that are likely related to under-coordinated lead ions and methylammonium vacancies to result in the PL blinking observed here.

  7. Development of crystals based in cesium iodide for application as radiation detectors

    International Nuclear Information System (INIS)

    Inorganic scintillators with fast luminescence decay time, high density and high light output have been the object of studies for application in nuclear physics, high energy physics, nuclear tomography and other fields of science and engineering. Scintillation crystals based on cesium iodide (CsI) are matters with relatively low higroscopy, high atomic number, easy handling and low cost, characteristics that favor their use as radiation detectors. In this work, the growth of pure CsI crystals, CsI:Br and CsI:Pb, using the Bridgman technique, is described. The concentration of the bromine doping element (Br) was studied in the range of 1,5x10-1 M to 10-2 M and the lead (Pb) in the range of 10-2 M to 5x10-4 M. To evaluate the scintillators developed, systematic measurements were carried out for luminescence emission and luminescence decay time for gamma radiation, optical transmittance assays, Vickers micro-hardness assays, determination of the doping elements distribution along the grown crystals and analysis of crystals response to the gamma radiation in the energy range of 350 keV to 1330 keV and alpha particles from a 241Am source, with energy of 5.54 MeV. It was obtained 13 ns to 19 ns for luminescence decay time for CsI:Br and CsI:Pb crystals. These results were very promising. The results obtained for micro-hardness showed a significant increase in function of the doping elements concentration, when compared to the pure CsI crystal, increasing consequently the mechanical resistance of the grown crystals. The validity of using these crystals as radiation sensors may be seen from the results of their response to gamma radiation and alpha particles. (author)

  8. Synthesis, growth and characterization of cadmium manganese thiocyanate (CMTC) crystal

    Science.gov (United States)

    Paramasivam, P.; Raja, C. Ramachandra

    2011-09-01

    Single crystals of cadmium manganese thiocyanate, CdMn(SCN)4 (CMTC) have been successfully synthesized and grown by slow evaporation solution growth technique using water as solvent at room temperature. The crystal was characterized by different techniques for finding its suitability for device fabrications. From the single crystal XRD the crystal system was identified as tetragonal. The functional groups were identified from FTIR analysis. The optical studies have been carried out and found that the tendency of transmission observed from the specimen with respect to the wavelength of light is practically more suitable for the present trends in communication engineering. From the thermal analysis the decomposing temperature of the grown crystal is more significant when compared with the studies performed earlier.

  9. Temperature anomalies of optical properties in cadmium diphosphide crystal

    International Nuclear Information System (INIS)

    The temperature dependence of refractive indices of ordinary and extraordinary rays (no, ne) in the temperature region 20-110 degrees Celsius for different directions in cadmium diphosphide crystal are presented in the given work. It is obtained that no and n increase with temperature growth. It is shown the thermo optical coefficient for ne depends on direction of laser beam relatively optical axis of the crystal and for no it doesn't depend. Several anomalies in the form of steps and bends are revealed on the curves of the temperature dependence of refractive indices. The detected features are connected with the transitions between commensurate and incommensurate phases. (authors)

  10. Divalent europium doped and un-doped calcium iodide scintillators: Scintillator characterization and single crystal growth

    Energy Technology Data Exchange (ETDEWEB)

    Boatner, L.A., E-mail: boatnerla@ornl.gov [Center for Radiation Detection Materials & Systems, Oak Ridge National Laboratory, Oak Ridge, TN 37831 (United States); Materials Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831 (United States); Ramey, J.O., E-mail: rameyjo@ornl.gov [Center for Radiation Detection Materials & Systems, Oak Ridge National Laboratory, Oak Ridge, TN 37831 (United States); Kolopus, J.A., E-mail: kolopusja@ornl.gov [Center for Radiation Detection Materials & Systems, Oak Ridge National Laboratory, Oak Ridge, TN 37831 (United States); Materials Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831 (United States); Neal, John S., E-mail: nealjs1@ornl.gov [Center for Radiation Detection Materials & Systems, Oak Ridge National Laboratory, Oak Ridge, TN 37831 (United States); Nuclear Science and Isotope Technology Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831 (United States)

    2015-06-21

    The alkaline-earth scintillator, CaI{sub 2}:Eu{sup 2+}, was initially discovered around 1964 by Hofstadter, Odell, and Schmidt. Serious practical problems quickly arose, however, that were associated with the growth of large monolithic single crystals of this material due to its lamellar, mica-like structure. As a result of its theoretically higher light yield, CaI{sub 2}:Eu{sup 2+} has the potential to exceed the excellent scintillation performance of SrI{sub 2}:Eu{sup 2+}. In fact, theoretical predictions for the light yield of CaI{sub 2}:Eu{sup 2+} scintillators suggested that an energy resolution approaching 2% at 662 keV could be achievable. As in the case of the early SrI{sub 2}:Eu{sup 2+} scintillator, the performance of CaI{sub 2}:Eu{sup 2+} scintillators has traditionally suffered due, at least in part, to outdated materials synthesis, component stoichiometry/purity, and single-crystal-growth techniques. Based on our recent work on SrI{sub 2}:Eu{sup 2+} scintillators in single-crystal form, we have developed new techniques that are applied here to CaI{sub 2}:Eu{sup 2+} and pure CaI{sub 2} with the goal of growing large un-cracked crystals and, potentially, realizing the theoretically predicted performance of the CaI{sub 2}:Eu{sup 2+} form of this material. Calcium iodide does not adhere to modern glassy carbon Bridgman crucibles—so there should be no differential thermal-contraction-induced crystal/crucible stresses on cooling that would result in crystal cracking of the lamellar structure of CaI{sub 2}. Here we apply glassy carbon crucible Bridgman growth, high-purity growth-charge compounds, our molten salt processing/filtration technique, and extended vacuum-melt-pumping methods to the growth of both CaI{sub 2}:Eu{sup 2+} and un-doped CaI{sub 2}. Large scintillating single crystals were obtained, and detailed characterization studies of the scintillation properties of CaI{sub 2}:Eu{sup 2+} and pure CaI{sub 2} single crystals are presented that include

  11. Crystal structure of 4-{2-[4-(dimethylaminophenyl]diazen-1-yl}-1-methylpyridinium iodide

    Directory of Open Access Journals (Sweden)

    Katherine Chulvi

    2015-12-01

    Full Text Available The molecular geometry of the ionic title compound, C14H17N4+·I− or DAZOP+·I−, is essentially featureless. Regarding the crystal structure, in addition to the obvious cation–anion Coulombic interactions, the packing is mostly directed by non-covalent interactions involving both ring systems, as well as the iodide anion. It consists of cationic molecules aligned along [101] and disposed in an antiparallel fashion while linked into π-bonded dimeric entities by a stacking contact involving symmetry-related phenyl rings, with a centroid–centroid distance of 3.468 (3 Å and a slippage of 0.951 Å. The dimers are, in addition, sustained by a number of C—H...I and I...π (I...centroid = 3.876 Å interactions involving the anion. Finally, interdimeric contacts are of the C—H...I and C—H...π types.

  12. Crystal growth and characterization of L-valine cadmium acetate a semiorganic NLO crystals

    Science.gov (United States)

    Chandrasekaran, J.; Ilayabarathi, P.; Maadeswaran, P.

    2012-08-01

    A new semiorganic nonlinear optical material, L-valine cadmium acetate, was grown successfully from aqueous solution by slow evaporation method. The grown crystals characterized by using Powder X-ray diffraction analysis confirms the structure of the grown title compound. The functional groups have been identified using FTIR spectral data. Transmittance compound was analyzed by using UV-vis spectrum. The thermal behavior of the grown crystal was determined with the aid of thermogravimetric analysis (TGA), differential thermal analysis (DTA) and differential scanning calorimetry (DSC). The dielectric constant was studied as a function of frequency for various temperatures. The grown crystal has positive photoconductivity nature. The fluorescence spectrum of the crystal was recorded and its optical band gap is about 3.4479 eV. Second order nonlinear optical property of the grown crystal has been confirmed by modified Kurtz-Perry powder second harmonic generation (SHG) test.

  13. Study on thermal annealing of cadmium zinc telluride (CZT) crystals

    Energy Technology Data Exchange (ETDEWEB)

    Yang, G.; Bolotnikov, A.E.; Fochuk, P.M.; Camarda, G.S.; Cui, Y.; Hossain, A.; Kim, K.; Horace, J.; McCall, B.; Gul, R.; Xu, L.; Kopach, O.V.; and James, R.B.

    2010-08-01

    Cadmium Zinc Telluride (CZT) has attracted increasing interest with its promising potential as a room-temperature nuclear-radiation-detector material. However, different defects in CZT crystals, especially Te inclusions and dislocations, can degrade the performance of CZT detectors. Post-growth annealing is a good approach potentially to eliminate the deleterious influence of these defects. At Brookhaven National Laboratory (BNL), we built up different facilities for investigating post-growth annealing of CZT. Here, we report our latest experimental results. Cd-vapor annealing reduces the density of Te inclusions, while large temperature gradient promotes the migration of small-size Te inclusions. Simultaneously, the annealing lowers the density of dislocations. However, only-Cd-vapor annealing decreases the resistivity, possibly reflecting the introduction of extra Cd in the lattice. Subsequent Te-vapor annealing is needed to ensure the recovery of the resistivity after removing the Te inclusions.

  14. Comment on the paper: Synthesis, growth and characterization of cadmium manganese thiocyanate (CMTC) crystal

    OpenAIRE

    Srinivasan, Bikshandarkoil R.

    2015-01-01

    The authors of the title paper (Spectrochim. Acta 79A (2011) 340-343) report the crystal growth of cadmium manganese thiocyanate CdMn(SCN)4 and its characterization by single crystal X-ray diffraction and infrared spectrum. Many points of criticism, concerning the crystal growth and reported experimental data are highlighted in this report.

  15. Crystal Structure and Photoluminescence of a Tetranuclear Cadmium Complex

    Institute of Scientific and Technical Information of China (English)

    史娟; 张尊听

    2012-01-01

    A novel tetranuclear cadmium complex ([{Cd(CIsHsOTS)(H20)(DMSO)}3{Cd(CtsH807S)(H20)2}]. 3DMSO.H20) was obtained by the self-assembly of Cd(II) with 5,7-dihydroxyflavone-6-sulfonate. The complex was characterized by IH NMR, IR, elemental analysis and X-ray single-crystal diffraction studies. It crystallizes in triclinic, space group P]-. In the complex, the chelate atoms of Cd(II) are all from oxygen. Four Cd(II) are con- nected via the carbonyl and 5-hydroxyanion of four ligands and form an approximate square. Four ligands locate at two sides of the square, and two of them at the same side are almost parallel and exist aromatic n-n stacking. Ligands on the opposite side of the square are nearly perpendicular. The result of the luminescent studies indicated that the solid of the complex shwed photoluminescent properties because of a combination of coordination, hydro- gen bonding and n-n stacking interaction in the molecule structure. The complex emits green fluorescence (2em= 496 nrn) when it is excited at the wavelength of 440 nm.

  16. Neutron Detection with Mercuric Iodide

    Energy Technology Data Exchange (ETDEWEB)

    Bell, Z.A.

    2003-06-17

    Mercuric iodide is a high-density, high-Z semiconducting material useful for gamma ray detection. This makes it convertible to a thermal neutron detector by covering it with a boron rich material and detecting the 478 keV gamma rays resulting from the {sup 10}B(n, {alpha}){sup 7}Li* reaction. However, the 374 barn thermal capture cross section of {sup nat}Hg, makes the detector itself an attractive absorber, and this has been exploited previously. Since previous work indicates that there are no low-energy gamma rays emitted in coincidence with the 368 keV capture gamma from the dominant {sup 199}Hg(n, {gamma}){sup 200}Hg reaction, only the 368 keV capture gamma is seen with any efficiency a relatively thin (few mm) detector. In this paper we report preliminary measurements of neutrons via capture reactions in a bare mercuric iodide crystal and a crystal covered in {sup 10}B-loaded epoxy. The covered detector is an improvement over the bare detector because the presence of both the 478 and 368 keV gamma rays removes the ambiguity associated with the observation of only one of them. Pulse height spectra, obtained with and without lead and cadmium absorbers, showed the expected gamma rays and demonstrated that they were caused by neutrons.

  17. Modeling high speed growth of large rods of cesium iodide crystals by edge-defined film-fed growth (EFG)

    Science.gov (United States)

    Yeckel, Andrew

    2016-09-01

    A thermocapillary model of edge-defined film-fed growth (EFG) is developed to analyze an experimental system for high speed growth of cesium iodide as a model system for halide scintillator production. The model simulates heat transfer and fluid dynamics in the die, melt, and crystal under conditions of steady growth. Appropriate mass, force, and energy balances are used to compute self-consistent shapes of the growth interface and melt-vapor meniscus. The model is applied to study the effects of growth rate, die geometry, and furnace heat transfer on the limits of system operability. An inverse problem formulation is used to seek operable states at high growth rates by adjusting the overall temperature level and thermal gradient in the furnace. The model predicts that steady growth is feasible at rates greater than 20 mm/h for crystals up to 18 mm in diameter under reasonable furnace gradients.

  18. High pressure electrical resistivity study on nonlinear bis thiourea cadmium chloride (BTCC) single crystal

    Energy Technology Data Exchange (ETDEWEB)

    Ariponnammal, S.; Radhika, S. [Department of Physics, Gandhigram Rural Institute, Deemed University, Gandhigram - 624 302, Dindigul District, Tamil Nadu (India); Selva Vennila, R. [Department of Physics, Anna University, Chennai - 600 025 (India); Arumugam, S. [Department of Physics, Bharathidasan University, Trichy (India)

    2005-09-01

    The Bis Thiourea Cadmium Chloride (BTCC) crystals have been crystallized by slow evaporation technique. The lattice parameters of the grown crystals have been determined by the Energy dispersive x-ray diffraction technique (EDXRD) and the structure has been confirmed. The high pressure electrical resistivity study have been carried out on this crystal and the results have been reported here. (copyright 2005 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  19. Crystal Structure and Characterization of a New Eight Coordinated Cadmium Complex

    Energy Technology Data Exchange (ETDEWEB)

    Hakimi, Mohammad; Moeini, Keyvan; Mardani, Zahra; Khorrami, Farzaneh [Payame Noor Univ., Tehran (Iran, Islamic Republic of)

    2013-06-15

    In this work, a new cadmium complex [Cd(L)(CH{sub 3}COO){sub 2}]-2H{sub 2}O (1) with the ligand L, N,N'-bis(2-pyridinecar-boxalidene)-1,2-cyclohexanediamine was prepared and identified by elemental analysis, FT-IR, Raman, {sup 1}H NMR spectroscopy and single-crystal X-ray diffraction. The cadmium atom in the crystal structure of 1 has distorted triangular dodecahedral geometry by coordination of the four nitrogen atoms of L and four oxygen atoms of the two acetate ions. Two water molecules are also incorporated in the crystal network. The O-H···O hydrogen bonds present in the crystal structure of 1. In this work, three structural surveys including coordination numbers of the cadmium atom, coordination modes of L and resonance in pyridine-2-ylmethanimine-based compounds are presented.

  20. Development of the mercury iodide semiconductor crystal for application as a radiation detector

    International Nuclear Information System (INIS)

    In this work, the establishment of a technique for HgI growth and preparation of crystals, for use as room temperature radiation semiconductor detectors is described. Three methods of crystal growth were studied while developing this work: physical vapor transport (PVT); saturated solution of HgI2, using two different solvents; (a) dimethyl sulfoxide (DMSO) and (b) acetone, and the Bridgman method. In order to evaluate the obtained crystals by the three methods, systematic measurements were carried out for determining the stoichiometry, structure, orientation, surface morphology and impurity of the crystal. The influence of these physical chemical properties on the crystals development was studied, evaluating their performance as radiation detectors. The X-ray diffractograms indicated that the crystals were, preferentially, oriented in the (001) e (101) directions with tetragonal structure for all crystals. Nevertheless, morphology with a smaller deformation level was observed for the crystal obtained by the PVT technique, comparing to other methods. Uniformity on the surface layer of the PVT crystal was detected, while clear incrustations of elements distinct from the crystal could be viewed on the DMSO crystal surface. The best results as to radiation response were found for the crystal grown by physical vapor transport. Significant improvement in the HgIz2 radiation detector performance was achieved for purer crystals, growing the crystal twice by PVT technique. (author)

  1. Crystallization of a perovskite film for higher performance solar cells by controlling water concentration in methyl ammonium iodide precursor solution

    Science.gov (United States)

    Adhikari, Nirmal; Dubey, Ashish; Gaml, Eman A.; Vaagensmith, Bjorn; Reza, Khan Mamun; Mabrouk, Sally Adel Abdelsalam; Gu, Shaopeng; Zai, Jiantao; Qian, Xuefeng; Qiao, Qiquan

    2016-01-01

    An optimal small amount of water added into methyl ammonium iodide (MAI) solution in isopropyl alcohol (IPA) helps perovskite crystallization and leads to larger grain size from sequential deposition of perovskite films. The concentration of water was varied from 1% to 7% (vol% of IPA) in MAI solution and optical absorption, crystallization, morphology of perovskite films and their photovoltaic performance were studied in perovskite solar cells. 5% by volume was found to lead to preferential crystallization in the (110) plane with grain size about three times that of perovskite films prepared without adding water into the MAI solution. The optimal water concentration of 5% by volume in the MAI solution led to average perovskite grain size of ~600 nm and solar cell efficiency of 12.42% at forward scan with a rate of 0.5 V s-1. Device performance decreases after increasing water concentration beyond 5% in the MAI solution due to formation of the PbI2 phase. Transient photocurrent and photovoltage measurements show the shortest charge transport time at 0.99 μs and the longest charge carrier life time at 13.6 μs for perovskite films prepared from 5% water in MAI solution, which improved perovskite solar cell efficiency from 9.04% to 12.42%.An optimal small amount of water added into methyl ammonium iodide (MAI) solution in isopropyl alcohol (IPA) helps perovskite crystallization and leads to larger grain size from sequential deposition of perovskite films. The concentration of water was varied from 1% to 7% (vol% of IPA) in MAI solution and optical absorption, crystallization, morphology of perovskite films and their photovoltaic performance were studied in perovskite solar cells. 5% by volume was found to lead to preferential crystallization in the (110) plane with grain size about three times that of perovskite films prepared without adding water into the MAI solution. The optimal water concentration of 5% by volume in the MAI solution led to average perovskite

  2. Potassium Iodide

    Science.gov (United States)

    Potassium iodide is used to protect the thyroid gland from taking in radioactive iodine that may be ... damage the thyroid gland. You should only take potassium iodide if there is a nuclear radiation emergency ...

  3. Chemical conversion of cisplatin and carboplatin with histidine in a model protein crystallized under sodium iodide conditions

    Energy Technology Data Exchange (ETDEWEB)

    Tanley, Simon W. M.; Helliwell, John R., E-mail: john.helliwell@manchester.ac.uk [University of Manchester, Brunswick Street, Manchester M13 9PL (United Kingdom)

    2014-08-29

    Crystals of HEWL with cisplatin and HEWL with carboplatin grown in sodium iodide conditions both show a partial chemical transformation of cisplatin or carboplatin to a transiodoplatin (PtI{sub 2}X{sub 2}) form. The binding is only at the N{sup δ} atom of His15. A further Pt species (PtI{sub 3}X) is also seen, in both cases bound in a crevice between symmetry-related protein molecules. Cisplatin and carboplatin are platinum anticancer agents that are used to treat a variety of cancers. Previous X-ray crystallographic studies of carboplatin binding to histidine in hen egg-white lysozyme (HEWL) showed a partial chemical conversion of carboplatin to cisplatin owing to the high sodium chloride concentration used in the crystallization conditions. Also, the co-crystallization of HEWL with carboplatin in sodium bromide conditions resulted in the partial conversion of carboplatin to the transbromoplatin form, with a portion of the cyclobutanedicarboxylate (CBDC) moiety still present. The results of the co-crystallization of HEWL with cisplatin or carboplatin in sodium iodide conditions are now reported in order to determine whether the cisplatin and carboplatin converted to the iodo form, and whether this took place in a similar way to the partial conversion of carboplatin to cisplatin in NaCl conditions or to transbromoplatin in NaBr conditions as seen previously. It is reported here that a partial chemical transformation has taken place to a transplatin form for both ligands. The NaI-grown crystals belonged to the monoclinic space group P2{sub 1} with two molecules in the asymmetric unit. The chemically transformed cisplatin and carboplatin bind to both His15 residues, i.e. in each asymmetric unit. The binding is only at the N{sup δ} atom of His15. A third platinum species is also seen in both conditions bound in a crevice between symmetry-related molecules. Here, the platinum is bound to three I atoms identified based on their anomalous difference electron densities

  4. Crystallization of a perovskite film for higher performance solar cells by controlling water concentration in methyl ammonium iodide precursor solution.

    Science.gov (United States)

    Adhikari, Nirmal; Dubey, Ashish; Gaml, Eman A; Vaagensmith, Bjorn; Reza, Khan Mamun; Mabrouk, Sally Adel Abdelsalam; Gu, Shaopeng; Zai, Jiantao; Qian, Xuefeng; Qiao, Qiquan

    2016-02-01

    An optimal small amount of water added into methyl ammonium iodide (MAI) solution in isopropyl alcohol (IPA) helps perovskite crystallization and leads to larger grain size from sequential deposition of perovskite films. The concentration of water was varied from 1% to 7% (vol% of IPA) in MAI solution and optical absorption, crystallization, morphology of perovskite films and their photovoltaic performance were studied in perovskite solar cells. 5% by volume was found to lead to preferential crystallization in the (110) plane with grain size about three times that of perovskite films prepared without adding water into the MAI solution. The optimal water concentration of 5% by volume in the MAI solution led to average perovskite grain size of ∼600 nm and solar cell efficiency of 12.42% at forward scan with a rate of 0.5 V s(-1). Device performance decreases after increasing water concentration beyond 5% in the MAI solution due to formation of the PbI2 phase. Transient photocurrent and photovoltage measurements show the shortest charge transport time at 0.99 μs and the longest charge carrier life time at 13.6 μs for perovskite films prepared from 5% water in MAI solution, which improved perovskite solar cell efficiency from 9.04% to 12.42%.

  5. Red mercuric iodide crystals obtained by isothermal solution evaporation: Characterization for mammographic X-ray imaging detectors

    Energy Technology Data Exchange (ETDEWEB)

    Caldeira, A.M.F.; Ugucioni, J.C.; Mulato, M.

    2014-02-11

    Millimeter-sized mercury iodide crystals were obtained by the isothermal evaporation technique using dimethylformamide (DMF), diethyl-ether/DMF mixture and THF. Different concentrations (18 mM and 400 mM) and solution temperature (25–80 °C) were used to obtain varied evaporation rates (0.1×10{sup −4}–5000×10{sup −4} ml/h). Different crystal sizes and shapes were obtained by changing solvents, mixture and initial solution volume. According to X-ray diffraction the samples are monocrystalline. The top surface was investigated by SEM. Optical band-gaps above 2 eV were obtained from photoacoustic spectroscopy. Photoluminescence spectra indicated band-to-band electronic transitions, and the presence of sub-band gap states. Excitons, structural defects and the presence of impurities are discussed and correlated to the electrical measurements. Crystals obtained using pure DMF as solvent showed better general properties, including under the exposure to mammographic X-ray energy range that led to sensibility of about 25 μC/Rcm{sup 2}.

  6. Growth and Characterizations of Pure and Calcium Doped Cadmium Tartrate Crystals by Silica Gel Method

    Directory of Open Access Journals (Sweden)

    N. S. Patil

    2014-10-01

    Full Text Available In the present course of investigation, pure and calcium doped cadmium tartrate crystals were grown in silica gel at room temperature. The optimum conditions were obtained by varying various parameters such as pH of gel, concentration of gel, gel setting time, concentration of reactants etc. Crystals having different morphologies were obtained such as whitish semitransparent, star shaped, needle shaped. Especially, effect of doping of calcium into cadmium tartrate has been studied with respect of size and transparency. It is found that doping enhances the size and transparency of the crystals. As-grown crystals were characterized using scanning electronic microscope (SEM, UV, Energy dispersive X-ray spectroscopy (EDAX.

  7. Structural, Microhardness, Photoconductivity, and Dielectric Properties of Tris(thiourea Cadmium Sulphate Single Crystals

    Directory of Open Access Journals (Sweden)

    A. P. Arthi

    2014-01-01

    Full Text Available Semiorganic nonlinear optical tris(thiourea cadmium sulphate (TTCS single crystals were grown by slow evaporation method. The crystal system, cell parameter of the grown crystal, was identified by powder X-ray diffraction study. The self-focusing Z-scan technique has been employed to observe the third-order nonlinear optical property of the grown crystal. The mechanical property of the grown crystal was examined by using Vicker’s microhardness test. Chemical etching studies were made on the TTCS crystal using water as an etchant. The dark current and photocurrent properties of the crystal were estimated by using photoconductivity study. The dielectric constant of grown crystal was studied in different temperature by varying applied frequencies.

  8. Thermal and Mechanical Properties of a Complex Nonlinear Optical Material: Cadmium Mercury Thiocyanate Crystal

    Institute of Scientific and Technical Information of China (English)

    YUAN Duo-Rong; XU Dong; ZHANG Guang-Hui; LIU Ming-Guo; GUO Shi-Yi; MENG Fan-Qing; LU Meng-Kai; FANG Qi; JIANG Min-Hua

    2000-01-01

    Institute of Crystal Materials and State Key Laboratory of Crystal Materials, Shandong University, Ji'nan 250100 (Received 18 March 2000) The data of the thermal expansion and specific heat of cadmium mercury thiocyanate crystal have been obtained. The specific heat is 0.7588J/g℃ at room temperature. The thermal expansion occurs in the direction parallel to the c-axis, and the thermal contraction occurs in the direction parallel to the a-axis. The thermal expansion is the same as the thermal contraction at 353 K. The relationship between thermal properties and crystal structure is discussed.

  9. Growth and characterization of L-histidine cadmium chloride monohydrate a semiorganic nonlinear optical crystals

    Science.gov (United States)

    Chandrasekaran, J.; Ilayabarathi, P.; Maadeswaran, P.; Mohamed Kutty, P.; Pari, S.

    2012-04-01

    L-histidine cadmium chloride monohydrate (LHCCM), a semiorganic nonlinear optical material was grown from aqueous solution by slow solvent evaporation method at room temperature. The LHCCM crystals were characterized by X-ray powder diffraction analysis. The presence of functional groups was identified through fourier transform infrared spectroscopy. Thermogravimetric and differential thermal analysis confirms that the crystal is stable up to 277 °C. The dielectric constant was studied as a function of frequency for various temperatures. The mechanical properties of the grown crystals have been studied using Vickers microhardness tester. The second harmonic generation behavior of LHCCM crystal was tested by modified Kurtz-Perry powder technique.

  10. Size-dependent phase transition in methylammonium lead iodide perovskite microplate crystals.

    Science.gov (United States)

    Li, Dehui; Wang, Gongming; Cheng, Hung-Chieh; Chen, Chih-Yen; Wu, Hao; Liu, Yuan; Huang, Yu; Duan, Xiangfeng

    2016-01-01

    Methylammonium lead iodide perovskite has attracted considerable recent interest for solution processable solar cells and other optoelectronic applications. The orthorhombic-to-tetragonal phase transition in perovskite can significantly alter its optical, electrical properties and impact the corresponding applications. Here, we report a systematic investigation of the size-dependent orthorhombic-to-tetragonal phase transition using a combined temperature-dependent optical, electrical transport and transmission electron microscopy study. Our studies of individual perovskite microplates with variable thicknesses demonstrate that the phase transition temperature decreases with reducing microplate thickness. The sudden decrease of mobility around phase transition temperature and the presence of hysteresis loops in the temperature-dependent mobility confirm that the orthorhombic-to-tetragonal phase transition is a first-order phase transition. Our findings offer significant fundamental insight on the temperature- and size-dependent structural, optical and charge transport properties of perovskite materials, and can greatly impact future exploration of novel electronic and optoelectronic devices from these materials. PMID:27098114

  11. Size-dependent phase transition in methylammonium lead iodide perovskite microplate crystals

    Science.gov (United States)

    Li, Dehui; Wang, Gongming; Cheng, Hung-Chieh; Chen, Chih-Yen; Wu, Hao; Liu, Yuan; Huang, Yu; Duan, Xiangfeng

    2016-04-01

    Methylammonium lead iodide perovskite has attracted considerable recent interest for solution processable solar cells and other optoelectronic applications. The orthorhombic-to-tetragonal phase transition in perovskite can significantly alter its optical, electrical properties and impact the corresponding applications. Here, we report a systematic investigation of the size-dependent orthorhombic-to-tetragonal phase transition using a combined temperature-dependent optical, electrical transport and transmission electron microscopy study. Our studies of individual perovskite microplates with variable thicknesses demonstrate that the phase transition temperature decreases with reducing microplate thickness. The sudden decrease of mobility around phase transition temperature and the presence of hysteresis loops in the temperature-dependent mobility confirm that the orthorhombic-to-tetragonal phase transition is a first-order phase transition. Our findings offer significant fundamental insight on the temperature- and size-dependent structural, optical and charge transport properties of perovskite materials, and can greatly impact future exploration of novel electronic and optoelectronic devices from these materials.

  12. A comparison of the use of sodium iodide and lanthanum bromide scintillation crystals for airborne surveys

    Science.gov (United States)

    Bailey, Derek M.

    The Environmental Protection Agency (EPA) Aerial Spectral Environmental Collection Technology (ASPECT) program performs aerial radiological and chemical characterization of geographical regions of interest. Airborne surveys are performed to characterize environmental radionuclide content, for mineral exploration, as well as for emergency scenarios such as major releases or lost sources. Two radiological detection systems are used by the ASPECT team for gamma-ray detection and characterization: lanthanum bromide [LaBr 3(Ce)] and sodium iodide [NaI(Tl)] scintillation systems. An aerial survey of a uranium mine in the western United States was performed using both NaI(Tl) and LaBr3(Ce) detection systems. Analyses of the survey data were performed with RadAssist software and applying International Atomic Energy Agency (IAEA) airborne gamma ray mapping guidelines. The data for the survey were corrected for cross-over, which is spectral interference from higher energy photons as a result of Compton scattering, height attenuation, cosmic ray contribution to signal, and Radon contribution to signal. Two radiation survey contours were generated from each discrete data set. Based on analysis of the uranium mine survey results, LaBr3(Ce) produced a product comparable to that of NaI(Tl). The LaBr3(Ce) detection system contained 1/16th the scintillating volume and had a total system weight that was 1/4th that of the NaI(Tl) system. LaBr3(Ce) demonstrated a clear advantage over NaI(Tl) detectors in system mobility, and weight factors in airborne gamma ray spectroscopy.

  13. Synthesis and Crystal Structure of a Novel 1D Mercury(II) Iodide Coordination Polymer Containing 40-Membered Macrocycle%Synthesis and Crystal Structure of a Novel 1D Mercury(II) Iodide Coordination Polymer Containing 40-Membered Macrocycle

    Institute of Scientific and Technical Information of China (English)

    GAN Xiao-Ping; KONG Ling; WU Peng; LV Chen; TU Yu-Long; CHEN Yi-Xin; ZHOU Hong-Ping; WU Jie-Ying; TIAN Yu-Peng

    2011-01-01

    A mercury coordination polymer [Hg3(TizT)216]n (Mr = 1921.72, TizT = 2,4,6- tri(imidazole- 1-yl)- 1,3,5-triazine) containing a 40-membered macrocycle which was constructed by four TizT ligands and four mercury(II) iodide molecules had been synthesized by the reaction of HgI2 with TizT. The complex was characterized by elemental analysis, FT-IR, ^1H NMR spectra and X-ray crystallography. The crystal of the complex belongs to the monoclinic system and C2/c space group with a = 35.840(5), b = 8.169(5), c = 14.980(5) A, β = 104.466(5)°, Z= 4, V= 4247(3) A^3, De = 3.006 g·cm^-3, μ= 15.223 mm^-1, F(000) = 3384, Rint = 0.0504, wR = 0.0833 and constructs a chair-like conformation of cyclohexane one by one, which forms a 1-D polymer through the fashion of fused ring aromatic hydrocarbon. The hydrogen bonds and π-π interactions shape the 2-D network structure. The two compounds excited weak fluorescence.

  14. Coloration of cadmium halide crystals due to reactor irradiation at low temperature

    International Nuclear Information System (INIS)

    The optical absorption spectra and ESR spectra of cadmium halide crystals were measured after the reactor irradiation at low temperature to study the coloration. The irradiated neutron dose was about 5 x 1017 n/cm2. In the measurement of ESR spectra, the crystal was rotated around the v-axis (the two-fold axis) in the magnetic field of fixed direction. The optical absorption spectra showed that the Cd3+ center was generated. From the analysis of the angular dependence of ESR spectra, the centers of C(2h) symmetry and the centers of D(3d) symmetry were considered to be generated. The models of these centers were considered, and the angular dependence was analyzed. It can be concluded from the present experiment that the coloration of cadmium halide crystals is recognized as the results of the reactor irradiation at low temperature. (Kato, T.)

  15. Influence of the orientation of methylammonium lead iodide perovskite crystals on solar cell performance

    Directory of Open Access Journals (Sweden)

    Pablo Docampo

    2014-08-01

    Full Text Available Perovskite solar cells are emerging as serious candidates for thin film photovoltaics with power conversion efficiencies already exceeding 16%. Devices based on a planar heterojunction architecture, where the MAPbI3 perovskite film is simply sandwiched between two charge selective extraction contacts, can be processed at low temperatures (<150 °C, making them particularly attractive for tandem and flexible applications. However, in this configuration, the perovskite crystals formed are more or less randomly oriented on the surface. Our results show that by increasing the conversion step temperature from room temperature to 60 °C, the perovskite crystal orientation on the substrate can be controlled. We find that films with a preferential orientation of the long axis of the tetragonal unit cell parallel to the substrate achieve the highest short circuit currents and correspondingly the highest photovoltaic performance.

  16. Synthesis and Crystal Structure of a New Mononuclear Cadmium(Ⅱ) Cryptate Derived from the Condensation of Tri(2-aminoethyl)amine with Glyoxal

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    A new mononuclear cadmium(Ⅱ) cryptate has been synthesized by [2+3] Schiff crystal structure, spectral characterization and molar conductivity show that cadmium(Ⅱ) is sixcoordinated (N6) into a distorted octahedral geometry.

  17. Influence of samarium impurity on spectral characteristics of calcium iodide crystals

    Science.gov (United States)

    Novosad, S. S.; Novosad, I. S.

    2013-03-01

    The influence of a SmBr3 impurity on optical absorption spectra and x-ray-, photo-, and thermally stimulated luminescence of CaI2 scintillator was studied in the temperature range 90-295 K. Activation of CaI2 from the melt by SmBr3 caused absorption bands related to 4 f 6 → 4 f 55 d electronic transitions in Sm2+ to appear in the spectra. Excitation and emission spectra of CaI2:SmBr3 (0.01 mol%) were represented mainly by bands characteristic of the matrix. The photoluminescence spectrum at 90 K upon optical excitation of the crystal in the impurity absorption region (λex = 280 nm) was approximated by individual Gaussian bands with maxima near 345, 395, 430, 470, 500, and 520 nm. The photoluminescence spectrum of CaI2:SmBr3 (0.5 mol%) at 295 K with excitation by radiation from an LGI-21 nitrogen laser (λex = 337.1 nm) was represented mainly by a band at 465 nm. The intensity of this band weakened, its maximum shifted to 470 nm, luminescence in the 520 nm region increased, and weak emission with a maximum near 585 nm was also observed upon lowering the crystal temperature to 90 K. Doping CaI2 with the Sm impurity decreased the yield and changed the spectral composition of its x-ray-luminescence. CaI2:SmBr3 stored a small light sum in shallow trapping levels upon x-ray excitation at 90 K. The nature of the emission and trapping centers in the investigated crystals was discussed.

  18. Synthesis and crystal structures of the first cadmium complexes of 3,5,6-tris(2-pyridyl)-1,2,4-triazine ligand

    Science.gov (United States)

    Marandi, Farzin; Jangholi, Mona; Hakimi, Mohammad; Rudbari, Hadi Amiri; Bruno, Giuseppe

    2013-03-01

    Three new cadmium(II) complexes, [Cd2(TPT)2(SCN)4]·H2O (1), [Cd(TPT)I2] (2) and [Cd(TPT)Br2] (3) ("TPT" is the abbreviation of 3,5,6-tris(2-pyridyl)-1,2,4-triazine), have been synthesized and characterized by elemental analysis, IR, 1H NMR spectroscopy, and studied by thermal gravimetric as well as X-ray single crystal diffraction. Two anions of four thiocyanate anions bridge two CdII ions to form a dinuclear complex, 1, and iodide and bromide ions produce two halide-coordinated [Cd(TPT)X2] complexes (X = I for 2 and Br for 3). Cadmium(II) in 1 is six coordinate, CdN4S2 and in 2 and 3 is five coordinate, CdN3I2 and CdN3Br2. The supramolecular features in these complexes are guided/controlled by N⋯O hydrogen bonding (in 1) and weak directional intermolecular Csbnd H⋯N, Cg⋯I, Csbnd H⋯Br and π-π interactions.

  19. A Photonic Crystal Laser from Solution Based Organo-Lead Iodide Perovskite Thin Films.

    Science.gov (United States)

    Chen, Songtao; Roh, Kwangdong; Lee, Joonhee; Chong, Wee Kiang; Lu, Yao; Mathews, Nripan; Sum, Tze Chien; Nurmikko, Arto

    2016-04-26

    Perovskite semiconductors are actively investigated for high performance solar cells. Their large optical absorption coefficient and facile solution-based, low-temperature synthesis of thin films make perovskites also a candidate for light-emitting devices across the visible and near-infrared. Specific to their potential as optical gain medium for lasers, early work has demonstrated amplified spontaneous emission and lasing at attractively low thresholds of photoexcitation. Here, we take an important step toward practically usable perovskite lasers where a solution-processed thin film is embedded within a two-dimensional photonic crystal resonator. We demonstrate high degree of temporally and spatially coherent lasing whereby well-defined directional emission is achieved near 788 nm wavelength at optical pumping energy density threshold of 68.5 ± 3.0 μJ/cm(2). The measured power conversion efficiency and differential quantum efficiency of the perovskite photonic crystal laser are 13.8 ± 0.8% and 35.8 ± 5.4%, respectively. Importantly, our approach enables scalability of the thin film lasers to a two-dimensional multielement pixelated array of microlasers which we demonstrate as a proof-of-concept for possible projection display applications. PMID:26997122

  20. Characterization of large cadmium zinc telluride crystals grown by traveling heater method

    DEFF Research Database (Denmark)

    Chen, H.; Awadalla, S.A.; Iniewski, K.;

    2008-01-01

    The focus of this paper is to evaluate thick, 20 X 20 X 10 and 10 X 10 X 10 mm(3), cadmium zinc telluride (CZT), Cd0.9Zn0.1Te, crystals grown using the traveling heater method (THIM). The phenomenal spectral performance and small size and low concentration of Te inclusions/precipitates of these c......The focus of this paper is to evaluate thick, 20 X 20 X 10 and 10 X 10 X 10 mm(3), cadmium zinc telluride (CZT), Cd0.9Zn0.1Te, crystals grown using the traveling heater method (THIM). The phenomenal spectral performance and small size and low concentration of Te inclusions...

  1. Nucleation Controlled Growth of Cadmium Oxalate Crystals in Agar Gel and Their Characterization

    Directory of Open Access Journals (Sweden)

    P. V. Dalal

    2013-01-01

    Full Text Available Perfect single crystals of cadmium oxalate have been grown using the slow and controlled reaction between cadmium acetate and oxalic acid in agar gel media at ambient temperature, resulting in the formation of insoluble product Cd(COO2. Different methods for growing crystals were adopted. The optimum conditions were employed in each method by varying the concentration of gel and reactants, gel setting time, and so forth. Prismatic, transparent single crystal about 20 times larger than the crystals obtained in various other methods at the interstitial by adding impurities in the gel was obtained. The grown crystals was characterized with the help of FT-IR studies and triclinic system of crystals were supported with lattice parameters a = 8.803 A0, b = 22.352 A0, c = 5.706 A0, α = 95.74 A0, β = 90.92 A0, γ = 117.01 A0, and V = 994.69 A03, calculated from X-ray diffractogram.

  2. New zinc-glycine-iodide complexes as a product of equilibrium and non-equilibrium crystallization in the Gly - ZnI2 - H2O system

    Science.gov (United States)

    Tepavitcharova, S.; Havlíček, D.; Matulková, I.; Rabadjieva, D.; Gergulova, R.; Plocek, J.; Němec, I.; Císařová, I.

    2016-09-01

    Equilibrium crystallization of two anhydrous complex compounds, [Zn(gly)2I2] and [Zn(gly)I2], and non-equilibrium crystallization of the [Zn3(H2O)4(μ-gly)2I6] complex have been observed in the Gly - ZnI2 - H2O system at 25°C. Different mixed zinc-glycine-iodide-aqua complexes exist in the studied solutions and those with the highest activity are responsible for the crystallization process. The stable [ZnI2O2(2Gly)]0 complexes are responsible for the large equilibrium crystallization field of the compound [Zn(gly)2I2] (monoclinic system, C2/c space group), in whose crystal structure they are incorporated as discrete distorted electroneutral tetrahedra. In zinc-iodide solutions with a low water activity it is more probable that the glycine zwitterions act as bidentate ligands and form polynuclear complexes. We assume the [ZnI2O2(2/2Gly)]0 infinite chains build the compound [Zn(gly)I2], for which we have found a narrow equilibrium crystallization field. We have failed to describe the crystal structure of this compound because of its limited stability in the air. Non-equilibrium crystallization of [Zn3(H2O)4(μ-gly)2I6] (triclinic system, P-1 space group) was demonstrated, with crystal structure built by trinuclear complexes [ZnI3O(1/2Gly)] [ZnO4(4H2O)O2(2/2Gly)(trans)][ZnI3O(1/2Gly)]. The FTIR and Raman spectra and also the thermal behaviour of the three compounds were discussed.

  3. Single crystal EPR study of VO(II)-doped cadmium potassium phosphate hexahydrate: A substitutional incorporation

    Indian Academy of Sciences (India)

    I Sougandi; T M Rajendiran; R Venkatesan; P Sambasiva Rao

    2002-10-01

    Single crystal EPR studies of VO(II)-doped cadmium potassium phosphate hexahydrate (CPPH) have been carried out at room temperature. The angular variation spectra in the three orthogonal planes indicate that the paramagnetic impurity has entered the lattice only substitutionally in place of Cd(II). Spin Hamiltonian parameters have been obtained from single crystal data. Powder spectra show a set of eight parallel and perpendicular features indicating the presence of only one site. The admixture coefficients have been calculated from the data, which agree well with the literature values.

  4. Growth and characterization of organometallic L-alanine cadmium chloride single crystal by slow evaporation technique

    Energy Technology Data Exchange (ETDEWEB)

    Bright, K.C., E-mail: brightmcc@yahoo.co.i [Department of Physics, Malankara Catholic College, Mariyagiri 629153, Tamil Nadu (India); Freeda, T.H. [Physics Research Center, S.T. Hindu College, Nagercoil 629002, Tamil Nadu (India)

    2010-09-15

    Single crystals of L-alanine cadmium chloride (LACC), an organometallic nonlinear optical material, have been grown by the slow evaporation technique. The grown crystals were subjected to various characterization techniques, such as single crystal and powder XRD, FTIR, UV-vis and TGA-DTA. The mechanical properties of the crystals show that this material belongs to the category of hard materials. Second harmonic generation was confirmed by the Kurtz and Perry powder technique. Electrical parameters, such as dielectric constant, dielectric loss, ac and dc conductivity and their corresponding activation energies have been studied. The low dielectric constant and dielectric loss suggest that this material is a good candidate for micro-electronic applications.

  5. Kinetics of plastic flow in cadmium telluride single crystal

    International Nuclear Information System (INIS)

    To identify the microscopic mechanism of plastic flow, we have analyzed temperature dependence of the critical resolved shear stress (CRSS) and of the activation volume for CdTe single crystals deformed in compression at various temperatures between 150 and 275K in terms of the kink-pair nucleation model of plastic flow in intrinsically strong crystals. In this model, stress-assisted thermally -activated kink-pair nucleation is considered to facilitate the passage of screw dislocation over a Peierls barrier. It is found that the yield stress tow depends on temperature T as tow/sup 0.5/ = A - BT, where A and B are positive constants, whereas the activation volume v varies with temperature T through the relation v/sup -I/ = C - DT, where C and D are positive constants. However, the slope of the straight line fitted to the data point in each case undergoes a change at a critical temperature 200K, indicating a transition in the rate process of yielding. For T direction in slip plane (Ill) was nearly equal to the distance between two neighboring Peierls valleys. But for T >200K, the maximum kink-pair height was almost twice the intervalley separation. We believe that the formation of kink-pair having a height larger than intervalley distance is hardly possible. Most probably stress-assisted thermally-activated breakaway of edge- dislocation segments from localized barriers, e.g. vacancies in above-equilibrium concentration, solid and gaseous residual impurities, dislocation debris formed during the stage of anelastic deformation of the specimen in the process of raising the stress from zero to the macro yield-point etc. determines the CRSS of nominally pure CdTe crystals in the temperature range 200 to 275K. (author)

  6. Synthesis and crystal structures of coordination compounds of pyridoxine with zinc and cadmium sulfates

    International Nuclear Information System (INIS)

    The pyridoxine complexes with zinc and cadmium sulfates are synthesized. The IR absorption spectra and thermal behavior of the synthesized compounds are described. Crystals of the [M(C8H11O3N)2(H2O)2]SO4 . 3H2O (M = Zn, Cd) compounds are investigated using X-ray diffraction. In the structures of both compounds, the M atoms are coordinated by the oxygen atoms of the deprotonated OH group and the CH2OH group retaining its own hydrogen atom, as well as by two H2O molecules, and have an octahedral coordination. The nitrogen atom of the heterocycle is protonated, so that the heterocycle acquires a pyridinium character. The cationic complexes form layers separated by the anions and crystallization water molecules located in between. The structural units of the crystals are joined together by a complex system of hydrogen bonds.

  7. Temperature studies of optical properties of cadmium diphosphide crystals

    International Nuclear Information System (INIS)

    The natural optical activity (NOA) and the refractive index are measured in the temperature intervals of 4.2 to 400 K and of 293 to 400 K, respectively. The dispersion of the NOA is best approximated by a single-term Drude formula. The parameters of dispersion formulas are given for various temperatures. A temperature dependence of NOA in CdP2 is found. The temperature variation of the CdP2 rotational ability is shown to be mainly due to the temperature shift of the corresponding optically active band at E = 2.4 eV. In the 360 to 380 K temperature range a break is observed in the temperature dependence of the specific rotation and the refractive index, while the temperature dependence of the gyration tensor component displays a characteristic feature with well defined maxima, which indicates the presence of a phase transition in CdP2 crystals in this temperature range. (author)

  8. Crystal structure and thermal behavior of a new cadmium indium oxalate

    International Nuclear Information System (INIS)

    A new mixed metal oxalate Cd3In2(C2O4)6·9H2O, with an open-framework structure, has been prepared from a precipitation method at room temperature. Its crystal structure has been solved from single-crystal diffraction data. The compound crystallizes with space group P6422 and the cell parameters are a=8.566(5) A, c=37.811(5) A, V=2403(2) A3, and Z=3 (R1=0.036). The three-dimensional structure is built from three types of MO8 (M=Cd, In) polyhedra, i.e., triangular dodecahedra, bicapped trigonal prisms and an undefined distorted eight-fold cadmium polyhedron. Relationships with the structures of the related cadmium zirconium oxalates are discussed. The structure overview suggests the possibility to conceive new oxalate-based materials with open-framework structures. The thermal behavior of the new compound is described in details from temperature-dependent X-ray powder diffraction and thermogravimetry measurements. The dehydration process of the precursor is reversible in its stability temperature range. The final product consists of a mixture of nanocrystalline CdIn2O4 and the simple oxides

  9. Hydrogen bonding in thiobenzamide synthon and its Cadmium complex: Crystal structure and Hirshfeld analysis

    Indian Academy of Sciences (India)

    INES RIGANE; SIWAR WALHA; ABDELHAMID BEN SALAH

    2016-09-01

    The thiobenzamid TBA and its Cd(II) complex, dichlorothiobenzamidecadmium(II) [Cd(TBA)Cl₂] complex has been synthesized and characterized by FT-IR, FT-Raman and UV–Vis spectroscopy. The crystal and molecular structure of TBA and [Cd(TBA)Cl₂] were determined by single crystal X-ray diffraction analysis. The molecular arrangement in the crystal structure of TBA can be described on the basis of supramolecular dimeric synthons built up by four independent TBA molecules stacked via N-H. . .S hydrogen bonds. The 3D Hirshfeld surfaces and the associated 2D fingerprint plots were investigated for intermolecular interactions. The N-H. . .S hydrogen bond percentages were estimated to be 23.1%, 22.9%, 30.6% and 27.3% of Hirshfeld surfaces area respectively for each TBA molecule. Synthons are associated through C–H. . . π interactions at percentage of 33.8%, 38.2%, 24.3% and 19.4% to result in 3D network. The dichlorothiobenzamide cadmium(II) complex bonded by sulfur atom of thiobenzamide shows a double chain of distorted octahedra around the cadmium atoms running along the a axis and the packing is stabilized by intra- and inter-chain hydrogen bonding interactions of the type N–H. . .Cl and aromatic π. . .π stacking interactions between ring centroids at 21.8% and 7.6% of the Hirshfeld surface area, respectively. The decomposition of the complex to cadmium sulfide has been investigated by thermogravimetric analysis (TGA).

  10. Influence of Anion and Mole Ratio on the Coordination Behavior of an NO2S3-Macrocycle: The Formation of a Dumbbell-Shaped Macrocyclic Cadmium(II) Iodide Complex.

    Science.gov (United States)

    Lee, Hyeong-Hwan; Lee, Eunji; Ju, Huiyeong; Kim, Seulgi; Park, In-Hyeok; Lee, Shim Sung

    2016-03-01

    Anion and mole ratio dependent formations of cadmium(II) complexes with an NO2S3-macrocycle (L) incorporating a pyridine subunit are reported. When the cadmium(II) salts (1-10 equiv) with different halide ions (Br(-) or I(-)) were reacted with L, CdBr2 afforded a monomer complex, [Cd(L)Br]2[Cd2Br6]·CH2Cl2 (1), with three separated parts in the whole mole ratio range: two 1:1 stoichiometric complex cation parts and one Cd2Br6 cluster anion part. After separation of 1 by filtration, [Cd(L)Br]2[CdBr4]·CH2Cl2 (2) with similar composition was afforded, except the cluster was isolated from the filtrate. Unlike the CdBr2 complexation, CdI2 afforded the mole ratio dependent products (3-5). Below 2.5 equiv of CdI2, [Cd(L)I]2[CdI4]·CH2Cl2 (3) and [Cd(L)I]2[Cd2I6]·0.5CH2Cl2 (4) with different cadmium(II) iodide clusters were isolated as kinetic (3) and a thermodynamic (4) products. Notably, the use of 3 equiv or above amount of CdI2 gave a dumbbell-shaped complex, {[Cd(L)]2(μ-Cd4I12)} (5), in which two mononuclear macrocyclic complex units are linked by a (μ-Cd4I12)(4-) cluster. To monitor the mole ratio dependency as well as their reactivities, the systematic powder X-ray diffraction (PXRD) analysis has also been applied.

  11. A dinuclear cadmium(II) Schiff base thiocyanato complex: crystal structure and fluorescence.

    Science.gov (United States)

    Shit, Shyamapada; Sankolli, Ravish; Guru Row, Tayur N

    2014-01-01

    A new dinuclear cadmium(II) complex, [Cd(L)(NCS)]2 (1) has been synthesized using a potentially tetradentate Schiff base ligand HL, 2-((E)-(2-(diethylamino)ethylimino)methyl)-6-methoxyphenol, obtained by the condensation of 2-diethylaminoethylamine and o-vanillin, and characterized by different physicochemical techniques. Crystal structure of the title complex was unambiguously established by single crystal X-ray diffraction which reveals that metal centers are connected by bridging phenolato and chelating methoxy oxygen atoms of the coordinating Schiff bases and embedded in severely distorted octahedral geometries. Fluorescence properties of the ligand and its complex, studied at room temperature indicate that later may serve as strong fluorescent emitter. PMID:24664327

  12. Development of crystals based in cesium iodide for application as radiation detectors; Desenvolvimento de cristais baseados em iodeto de cesio para aplicacao como detectores de radiacao

    Energy Technology Data Exchange (ETDEWEB)

    Pereira, Maria da Conceicao Costa

    2006-07-01

    Inorganic scintillators with fast luminescence decay time, high density and high light output have been the object of studies for application in nuclear physics, high energy physics, nuclear tomography and other fields of science and engineering. Scintillation crystals based on cesium iodide (CsI) are matters with relatively low higroscopy, high atomic number, easy handling and low cost, characteristics that favor their use as radiation detectors. In this work, the growth of pure CsI crystals, CsI:Br and CsI:Pb, using the Bridgman technique, is described. The concentration of the bromine doping element (Br) was studied in the range of 1,5x10{sup -1} M to 10{sup -2} M and the lead (Pb) in the range of 10{sup -2} M to 5x10{sup -4} M. To evaluate the scintillators developed, systematic measurements were carried out for luminescence emission and luminescence decay time for gamma radiation, optical transmittance assays, Vickers micro-hardness assays, determination of the doping elements distribution along the grown crystals and analysis of crystals response to the gamma radiation in the energy range of 350 keV to 1330 keV and alpha particles from a {sup 241}Am source, with energy of 5.54 MeV. It was obtained 13 ns to 19 ns for luminescence decay time for CsI:Br and CsI:Pb crystals. These results were very promising. The results obtained for micro-hardness showed a significant increase in function of the doping elements concentration, when compared to the pure CsI crystal, increasing consequently the mechanical resistance of the grown crystals. The validity of using these crystals as radiation sensors may be seen from the results of their response to gamma radiation and alpha particles. (author)

  13. A comparative study of pure and potassium doped cadmium mercury thiocyanate single crystals grown in silica gel

    Energy Technology Data Exchange (ETDEWEB)

    Kumari, P.N.S. [Department of Physics, Auxilium College, Vellore (India); Margaret, M.B. [Department of Physics, Arignar Anna Govt. College for Women, Walajapet (India); Kalainathan, S. [School of Science and Humanities, VIT University, Vellore (India)

    2009-02-15

    Pure and potassium doped cadmium mercury thiocyanate single crystals have been obtained from silica gel by the process of diffusion. The X-ray diffraction studies reveal the crystal lattice of both pure and doped crystals to be tetragonal. The crystalline perfection of the grown crystals were investigated by high resolution X-ray diffraction analysis and the quality of the crystals are found to be extremely good. Transmission and Fourier transform infrared spectra were recorded for the grown crystals. The TG/DTA analyses show that the crystals are highly thermally stable. The mechanical strength of the crystals were studied by Vickers microhardness test and a study of their second harmonic generation efficiency in comparison with urea has been made by performing Kurtz powder test. (copyright 2009 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  14. Mechanism of linear and nonlinear optical properties of bis-thiourea cadmium chloride single crystal

    International Nuclear Information System (INIS)

    Within the generalized gradient approximation (GGA), a calculation of the electronic structure of a semiorganic crystal named bis-thiourea cadmium chloride (BTCC) was performed, then the linear and nonlinear optical responses were obtained over a wide energy range, using a scissor energy of 1.30 eV, and our results are in good agreement with the experiments. The accurate full-potential projected augmented wave (FP-PAW) method was used. The prominent spectrum of the second harmonic generation (SHG) was successfully correlated with the dielectric function in terms of single- and double-photon resonances. Both the virtual electron (VE) and virtual hole (VH) processes make contributions to the SHG of BTCC crystal, and the VH process is enhanced by the Cd-centered tetrahedron. The SHG effect of the semiorganic material is attributed to the charge transfer (CT). The CT model for the semiorganic crystal is named as “M-ΠO⋯X”. “M” is a metal atom providing electrons, “ΠO” is a π-conjugated covalent of an organic molecule, and “X” is a high electronegativity atom. The CT across the BTCC molecule is along a π-electron conjugation covalence bond, and the delocalized electrons of sulfur provide an excellent bridge. The strong “pull” effect for the CT is due to the intramolecular hydrogen bonds provided by the chlorine with the high electron affinity.

  15. Study of crystalline perfection and thermal analysis of zinc cadmium thiocyanate single crystals grown in silica gel

    Energy Technology Data Exchange (ETDEWEB)

    Nisha Santha Kumari, P. [Department of Physics, Auxilium College, Vellore (India); Kalainathan, S. [School of Science and Humanities, VIT University, Vellore (India); Bhagavannarayana, G. [Materials Characterization Division, National Physical Laboratory, New Delhi (India)

    2008-03-15

    Zinc cadmium thiocyanate ZnCd(SCN){sub 4} abbreviated as ZCTC is a bimetallic thiocyanate complex that exhibits excellent nonlinear optical property. Single crystals of ZCTC have been grown in silica gel by the process of diffusion. Colorless transparent crystals of size 12 mm x 2 mm x 1.3 mm have been obtained. High resolution X-ray diffraction study was carried out to investigate the crystalline perfection of the grown crystal and the quality of the crystal was found to be quite good. Thermal stability of the grown crystal was investigated by thermogravimetric and differential thermal analyses. Fourier Transform Infrared spectrum was recorded to confirm the functional groups. Microhardness of the crystal is also studied. Being a nonlinear optical material, a comparative study of its second harmonic generation efficiency with urea has been made. (copyright 2007 WILEY -VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  16. Preparation and characterization of cadmium(II) halide complexes with N-substituted glycines, and the crystal structures of dichloro(N-methylglycine)cadmium(II) and diaquadichloro(N,N-dimethylglycine)cadmium(II)

    Energy Technology Data Exchange (ETDEWEB)

    Yamada, Junichi; Hashimoto, Haruki; Inomata, Yoshie; Takeuchi, Toshio [Jochi Univ., Tokyo (Japan). Faculty of Science and Technology

    1994-12-01

    Eight cadmium(II) halide complexes with N-methylglycine (sarcosine, Hsar), N,N-dimethylglycine (Hdmgly), and N,N,N-trimethylglycine (betaine, Hbet) have been prepared and characterized by using their infrared absorption spectra and thermal analyses. In addition, the crystal and molecular structures of [CdCl{sub 2}(Hsar)] (1) and [CdCl{sub 2}(Hdmgly)(H{sub 2}O){sub 2}] (2) were determined by a single-crystal X-ray diffraction method. The crystal data for these two complexes are as follows: Complex (1): monoclinic, space group P2{sub 1}/n, a=7.960(2), b=13.844(1), c=6.917(1) A, {beta}=92.42(2)deg, Z=4. Complex (2): monoclinic, space group P2{sub 1}/a, a=7.696(2), b=21.854(4), c=6.253(2) A, {beta}=103.69(2)deg, Z=4. These structures were solved by the heavy-atom method and refined by full-matrix least-square methods to final R values of 0.043 for 2533 reflections about 1 and 0.068 for 3615 reflections about 2, respectively. For 1 the structure consists of a one-dimensional polymer bridged by two chlorine atoms. The cadmium atom is hexa-coordinated, being ligated with two oxygen atoms of a carboxyl group and four chlorine atoms. For 2 the cadmium atom is in a distorted octahedral geometry, ligated by a carboxylato oxygen atom, two water molecules, and three chlorine atoms, in which one is terminal and the other two are bridging cadmium atoms to make a polymer. (author).

  17. Tunable Crystal-to-Crystal Phase Transition in a Cadmium Halide Chain Polymer

    Directory of Open Access Journals (Sweden)

    Ulli Englert

    2011-07-01

    Full Text Available The chain polymer [{Cd(μ-X2py2}1∞] (X = Cl, Br; py = pyridine undergoes a fully reversible phase transition between a monoclinic low-temperature and an orthorhombic high-temperature phase. The transformation can be directly monitored in single crystals and can be confirmed for the bulk by powder diffraction. The transition temperature can be adjusted by tuning the composition of the mixed-halide phase: Transition temperatures between 175 K up to the decomposition of the material at ca. 350 K are accessible. Elemental analysis, ion chromatography and site occupancy refinements from single-crystal X-ray diffraction agree with respect to the stoichiometric composition of the samples.

  18. Crystal Growth, Characterization and Fabrication of Cadmium Zinc Telluride-based Nuclear Detectors

    Science.gov (United States)

    Krishna, Ramesh M.

    In today's world, nuclear radiation is seeing more and more use by humanity as time goes on. Nuclear power plants are being built to supply humanity's energy needs, nuclear medical imaging is becoming more popular for diagnosing cancer and other diseases, and control of weapons-grade nuclear materials is becoming more and more important for national security. All of these needs require high-performance nuclear radiation detectors which can accurately measure the type and amount of radiation being used. However, most current radiation detection materials available commercially require extensive cooling, or simply do not function adequately for high-energy gamma-ray emitting nuclear materials such as uranium and plutonium. One of the most promising semiconductor materials being considered to create a convenient, field-deployable nuclear detector is cadmium zinc telluride (CdZnTe, or CZT). CZT is a ternary semiconductor compound which can detect high-energy gamma-rays at room temperature. It offers high resistivity (≥ 1010 O-cm), a high band gap (1.55 eV), and good electron transport properties, all of which are required for a nuclear radiation detector. However, one significant issue with CZT is that there is considerable difficulty in growing large, homogeneous, defect-free single crystals of CZT. This significantly increases the cost of producing CZT detectors, making CZT less than ideal for mass-production. Furthermore, CZT suffers from poor hole transport properties, which creates significant problems when using it as a high-energy gamma-ray detector. In this dissertation, a comprehensive investigation is undertaken using a successful growth method for CZT developed at the University of South Carolina. This method, called the solvent-growth technique, reduces the complexity required to grow detector-grade CZT single crystals. It utilizes a lower growth temperature than traditional growth methods by using Te as a solvent, while maintaining the advantages of

  19. Characterization of cadmium manganese telluride (Cd1-xMnxTe) crystals grown by floating zone method

    Science.gov (United States)

    Hossain, A.; Gu, G. D.; Bolotnikov, A. E.; Camarda, G. S.; Cui, Y.; Gul, R.; Roy, U. N.; Yang, G.; Liu, T.; Zhong, R.; Schneeloch, J.; James, R. B.

    2014-09-01

    Recently, Cadmium Manganese Telluride (CMT) emerged as a promising material for roomtemperature X- and gamma-ray detectors. However, our studies revealed several material defects primarily related to growth processes that are impeding the production of large single crystals with high resistivity and high mobility-lifetime product. In this work, we characterized various defects in materials grown by the floating zone method, including twins, Te inclusions, and dislocations, using our unique facilities. We also fabricated detectors from selected CMT crystals and tested their performance. This paper discusses our detailed findings on the material's properties and the performance of fabricated CMT detectors.

  20. Use of pixelated detectors for the identification of defects and charge collection effects in mercuric iodide (HgI2) single crystal material

    International Nuclear Information System (INIS)

    Physical structure of pixelated detectors provides a unique tool to evaluate the effects of different types of defects in the semiconductor material that is used to fabricate the detectors. The spectroscopic performance measured for individual pixels or groups of pixels can be used to correlate point defects or fields of inhomogeneities within the material with the charge collected from photoelectric events. A block of single crystal mercuric iodide of approximately 18x18 mm2 area and between 6 and 10 mm thick is prepared. The homogeneity of this material is then investigated with light in the transparent region for HgI2 using an optical microscope. Several types of defects can be identified in this way by the scattering of light, for example, single large inclusions or voids and areas of haziness consisting of fields of small inclusions. Standard procedures are used to fabricate from this block a pixelated detector with a 121-pixel anode structure. The performance of each pixel is measured, and differences in charge collection are correlated with the optical data. Measurement data are presented, and possible mechanisms of the interactions between the defects and the charge carriers are discussed.

  1. Growth, optical, electrical and photoconductivity studies of a novel nonlinear optical single crystal: Mercury cadmium chloride thiocyanate

    Science.gov (United States)

    Kumar, S. M. Ravi; Selvakumar, S.; Sagayaraj, P.; Anbarasi, A.

    2015-02-01

    SCN- ligand based organometallic non-linear optical mercury cadmium chloride thiocyanate (MCCTC) crystals are grown from water plus methanol mixed solvent by slow evaporation technique. The grown crystals are confirmed by single crystal X-ray diffraction analysis which reveals that the MCCTC belongs to rhombohedral system with R3c space group. MCCTC exhibits a SHG efficiency which is nearly 17 times more than that of KDP. The dielectric constant, dielectric loss measurements of the sample have been carried out for different frequencies (100 Hz to 5 MHz) and, temperatures (308 to 388 K) and the results are discussed. Photoconductivity study confirms that the title compound possesses negative photoconducting nature. The surface morphology of MCCTC was also investigated

  2. Effect of cadmium sulfide nanorod content on Freedericksz threshold voltage, splay and bend elastic constants in liquid-crystal nanocomposites

    Science.gov (United States)

    Nayek, Prasenjit; Karan, Santanu; Kundu, Sudarshan; Lee, Seung Hee; Das Gupta, Sudeshna; Roy, Soumen Kumar; Roy, Subir Kumar

    2012-06-01

    This report describes how doping liquid crystals (LC) with rod-like hexagonal semiconductor nanoprisms alters the dielectric and elastic properties of the composites as compared with a pristine nematic liquid crystal (NLC). Cadmium sulfide nanorods were synthesized via the solvothermal process and blended with a NLC. Nanorods were highly miscible with NLC and produced a topological defect-free texture up to a certain limit. A good dark state was achieved during the homeotropic configuration of the cell within that limit. Appreciable changes in splay and bend elastic constants of the LCs were observed after blending with nanorods. Long-range order was established in the hybrid system, and consequently the anisotropy was increased. The threshold voltage decreased dramatically by ˜31%. Dielectric study revealed a high-frequency mode, which might be due to anchoring of the LC with nanorods.

  3. Construction of new iodide selective electrodes based on bis(trans-cinnamaldehyde)1,3-propanediimine(L) zinc(II) chloride [ZnLCl2] and bis(trans-cinnamaldehyde) 1,3-propanediimine(L) cadmium(II) chloride [CdLCl2

    International Nuclear Information System (INIS)

    New plasticized PVC membranes iodide selective electrodes have been prepared by incorporating bis(trans-cinnamaldehyde)1,3-propanediimine zinc(II) chloride [ZnLCl2] and bis(trans-cinnamaldehyde) 1,3-propandiimine cadmium(II) chloride [CdLCl2] on the surface of graphite disk electrodes. At optimum value of variables the proposed electrodes have selective response to iodide with respect to a number of inorganic and organic anions with near-Nernstian slopes of − 60 ± 1.9 and − 58.5 ± 1.9 mV/decade of iodide concentration over the range 1.0 × 10−6–1.0 × 10−1 M with detection limits of 4.0 × 10−7 and 3.0 × 10−7 M for the electrodes based on [ZnLCl2] and [CdLCl2], respectively. The electrodes based on both ionophores have response times of about (6 s), with stable reproducible response during 2 months, while their responses is independent of pH over the range 2.5–10.5. The proposed electrodes successfully have been applied for evaluation of iodide ion content in real samples with complicated matrices including water and pharmaceutical samples. - Highlights: ► New ionophores have been synthesized for the first time in our laboratory. ► The ionophores were made from inexpensive materials. ► These Schiff bases synthesized for Zn+2, Cd+2 ions.

  4. Construction of new iodide selective electrodes based on bis(trans-cinnamaldehyde)1,3-propanediimine(L) zinc(II) chloride [ZnLCl{sub 2}] and bis(trans-cinnamaldehyde) 1,3-propanediimine(L) cadmium(II) chloride [CdLCl{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Ghaedi, M., E-mail: m_ghaedi@mail.yu.ac.ir; Montazerozohori, M.; Mousavi, A.; Khodadoust, S.; Mansouri, M.

    2012-04-01

    New plasticized PVC membranes iodide selective electrodes have been prepared by incorporating bis(trans-cinnamaldehyde)1,3-propanediimine zinc(II) chloride [ZnLCl2] and bis(trans-cinnamaldehyde) 1,3-propandiimine cadmium(II) chloride [CdLCl2] on the surface of graphite disk electrodes. At optimum value of variables the proposed electrodes have selective response to iodide with respect to a number of inorganic and organic anions with near-Nernstian slopes of - 60 {+-} 1.9 and - 58.5 {+-} 1.9 mV/decade of iodide concentration over the range 1.0 Multiplication-Sign 10{sup -6}-1.0 Multiplication-Sign 10{sup -1} M with detection limits of 4.0 Multiplication-Sign 10{sup -7} and 3.0 Multiplication-Sign 10{sup -7} M for the electrodes based on [ZnLCl{sub 2}] and [CdLCl{sub 2}], respectively. The electrodes based on both ionophores have response times of about (6 s), with stable reproducible response during 2 months, while their responses is independent of pH over the range 2.5-10.5. The proposed electrodes successfully have been applied for evaluation of iodide ion content in real samples with complicated matrices including water and pharmaceutical samples. - Highlights: Black-Right-Pointing-Pointer New ionophores have been synthesized for the first time in our laboratory. Black-Right-Pointing-Pointer The ionophores were made from inexpensive materials. Black-Right-Pointing-Pointer These Schiff bases synthesized for Zn{sup +2}, Cd{sup +2} ions.

  5. Study on Extracting Low Concentration Cadmium from Zinc Hydrometallurgy System by Liquid Membrane Crystallizing Technique

    Institute of Scientific and Technical Information of China (English)

    1999-01-01

    The extraction of low concentration cadmium from a system containing high concentration zinc was studied and got CdS product directly. A new liquid membrane system taking DIPSA, TIBPS as carriers, (NH4)2S as precipitating agent was reported. Precipitating Cd2+ in the internal aq. phase that is used to treat sulfuric acid leaching solution of zinc oxide in zinc hydrometallurgy has gotten satisfied results of extracting cadmium from high concentration zinc. After one-stage of batch process under the optimum liquid membrane conditions, 98.6% transferring rate and 98.1% extracting rate of cadmium was obtained with only less than 1.0% transferring rate of zinc, and the feed solution can be purified very well.

  6. Synthesis, Crystal Structure and Electrochemical Properties of a Cadmium(II) Complex with α-Furoic Acid and 1,10-Phenanthroline

    Institute of Scientific and Technical Information of China (English)

    ZHANG Shao-Hua; LI Chang-Hong; LI Wei; YANG Ying-Qun

    2008-01-01

    A new cadmium complex [Cd(phen)3]·(ClO4)2·(α-FRA)·(H2O)3 was prepared by self-assembly of α-furoic acid, 1,10-phenanthroline (phen), and cadmium perchlorate. It crystal- lizes in the monoclinic system, space group P21/n, with a = 1.28130(15), b = 2.5957(3), c = 1.35449(16) nm, β = 109.395(2)o, V = 4.2492(9) nm3, Dc = 1.491 g/cm3, Z = 4, F(000) = 1926, GOOF = 1.023, the final R = 0.0729 and wR = 0.2086. The crystal structure analysis indicates that the cadmium ion is coordinated with six nitrogen atoms from six 1,10-phenanthroline molecules, giving a distorted octahedral coordination geometry. The cyclic voltametric behavior of the com- plex was also investigated.

  7. Models for Copper Dynamic Behavior in Doped Cadmium dl-Histidine Crystals: Electron Paramagnetic Resonance and Crystallographic Analysis.

    Science.gov (United States)

    Colaneri, Michael J; Teat, Simon J; Vitali, Jacqueline

    2015-11-12

    Electron paramagnetic resonance and crystallographic studies of copper-doped cadmium dl-histidine, abbreviated as CdDLHis, were undertaken to gain further understanding on the relationship between site structure and dynamic behavior in biological model complexes. X-ray diffraction measurements determined the crystal structure of CdDLHis at 100 and 298 K. CdDLHis crystallizes in the monoclinic space group P21/c with two cadmium complexes per asymmetric unit. In each complex, the Cd is hexacoordinated to two histidine molecules. Both histidines are l in one complex and d in the other. Additionally, each complex contains multiple waters of varying disorder. Single crystal EPR spectroscopic splitting (g) and copper hyperfine (A(Cu)) tensors at room temperature (principal values: g = 2.249, 2.089, 2.050; A(Cu) = -453, -30.5, -0.08 MHz) were determined from rotational experiments. Alignments of the tensor directions with the host structure were used to position the copper unpaired dx(2)-y(2) orbital in an approximate plane made by four proposed ligand atoms: the N-imidazole and N-amino of one histidine, and the N-amino and O-carboxyl of the other. Each complex has two such planes related by noncrystallographic symmetry, which make an angle of 65° and have a 1.56 Å distance between their midpoints. These findings are consistent with three interpretations that can adequately explain previous temperature-dependent EPR powder spectra of this system: (1) a local structural distortion (static strain) at the copper site has a temperature dependence significant enough to affect the EPR pattern, (2) the copper can hop between the two sites in each complex at high temperature, and (3) there exists a dynamic Jahn-Teller effect involving the copper ligands. PMID:26501364

  8. Horizontal Ampoule Growth and Characterization of Mercuric Iodide at Controlled Gas Pressures for X-Ray and Gamma Ray Spectrometers

    Energy Technology Data Exchange (ETDEWEB)

    McGregor, Douglas S. [Kansas State Univ., Manhattan, KS (United States). Semiconductor Materials and Radiological Technologies Lab., Dept. of Nuclear and Mechanical Engineering; Ariesanti, Elsa [Kansas State Univ., Manhattan, KS (United States). Semiconductor Materials and Radiological Technologies Lab., Dept. of Nuclear and Mechanical Engineering; Corcoran, Bridget [Kansas State Univ., Manhattan, KS (United States). Semiconductor Materials and Radiological Technologies Lab., Dept. of Nuclear and Mechanical Engineering

    2004-04-30

    The project developed a new method for producing high quality mercuric iodide crystals of x-ray and gamma spectrometers. Included are characterization of mercuric iodide crystal properties as a function of growth environment and fabrication and demonstration of room-temperature-operated high-resolution mercuric iodide spectrometers.

  9. Neutron Detection with Mercuric Iodide

    CERN Document Server

    Bell, Z A

    2003-01-01

    Mercuric iodide is a high-density, high-Z semiconducting material useful for gamma ray detection. This makes it convertible to a thermal neutron detector by covering it with a boron rich material and detecting the 478 keV gamma rays resulting from the sup 1 sup 0 B(n, alpha) sup 7 Li* reaction. However, the 374 barn thermal capture cross section of sup n sup a sup t Hg, makes the detector itself an attractive absorber, and this has been exploited previously. Since previous work indicates that there are no low-energy gamma rays emitted in coincidence with the 368 keV capture gamma from the dominant sup 1 sup 9 sup 9 Hg(n, gamma) sup 2 sup 0 sup 0 Hg reaction, only the 368 keV capture gamma is seen with any efficiency a relatively thin (few mm) detector. In this paper we report preliminary measurements of neutrons via capture reactions in a bare mercuric iodide crystal and a crystal covered in sup 1 sup 0 B-loaded epoxy. The covered detector is an improvement over the bare detector because the presence of both ...

  10. Synthesis and Crystal Structure of a New Cadmium(Ⅱ) Supramolecular Network Containing Chelating Imidazole-4-carboxylate Ligand

    Institute of Scientific and Technical Information of China (English)

    YIN Wei-Ping; LI Yan-Ge; MEI Xue-Lan; YAO Jing-Cai

    2009-01-01

    A new complex, [Cd(Himc)2(H2O)2] 1, obtained from imidazole-4-carboxylatic acid (H2imc) and Cd(ClO4)2·6H2O, has been synthesized. The crystal structure was determined by X-ray diffraction. The title compound crystallizes in the orthorhombic system, space group Pccn, with a = 7.4886(11), b = 11.9667(18), c = 13.550(2) A, V= 1214.3(3) A3, Z = 4, Mr= 370.60, Dc = 2.027 mg/m3, F(000) = 728,μ (MoKα) = 1.829 mm-1, the final R = 0.0243 and wR = 0.0591 for 1150 unique reflections with I > 2σ(I). The cadmium(Ⅱ) center in the title complex is coordinated with two oxygen and two nitrogen atoms from two bidentate chelated imidazole-4-carboxlate ligands together with two water molecules, giving a distorted octahedral coordination geometry. A one-dimensional hydrogen bonding chain is formed via intermolecular O--H…O hydrogen bonds, and such adjacent chains are further stacked through intermolecular π-π and hydrogen bonding interactions to form a 3D supramolecular framework. Complex 1 exhibits a fluorescent emission band at 290 nm (λex = 236 nm) in the solid state.

  11. Production of Molecular Iodine and Tri-iodide in the Frozen Solution of Iodide: Implication for Polar Atmosphere.

    Science.gov (United States)

    Kim, Kitae; Yabushita, Akihiro; Okumura, Masanori; Saiz-Lopez, Alfonso; Cuevas, Carlos A; Blaszczak-Boxe, Christopher S; Min, Dae Wi; Yoon, Ho-Il; Choi, Wonyong

    2016-02-01

    The chemistry of reactive halogens in the polar atmosphere plays important roles in ozone and mercury depletion events, oxidizing capacity, and dimethylsulfide oxidation to form cloud-condensation nuclei. Among halogen species, the sources and emission mechanisms of inorganic iodine compounds in the polar boundary layer remain unknown. Here, we demonstrate that the production of tri-iodide (I3(-)) via iodide oxidation, which is negligible in aqueous solution, is significantly accelerated in frozen solution, both in the presence and the absence of solar irradiation. Field experiments carried out in the Antarctic region (King George Island, 62°13'S, 58°47'W) also showed that the generation of tri-iodide via solar photo-oxidation was enhanced when iodide was added to various ice media. The emission of gaseous I2 from the irradiated frozen solution of iodide to the gas phase was detected by using cavity ring-down spectroscopy, which was observed both in the frozen state at 253 K and after thawing the ice at 298 K. The accelerated (photo-)oxidation of iodide and the subsequent formation of tri-iodide and I2 in ice appear to be related with the freeze concentration of iodide and dissolved O2 trapped in the ice crystal grain boundaries. We propose that an accelerated abiotic transformation of iodide to gaseous I2 in ice media provides a previously unrecognized formation pathway of active iodine species in the polar atmosphere.

  12. Application prospects of cadmium-containing crystals based on tungstates and double tungstates

    CERN Document Server

    Nagornaya, L; Apanasenko, A; Tupitsyna, I; Chernikov, V; Vostretsov, V

    2002-01-01

    Tungstate and double tungstate crystals of high scintillation efficiency and detectors based on them are applied widely in the medical imaging and radiation monitoring because of their high sensitivity to the ionizing radiation, small radiation length, high radiation hardness, low afterglow level. In this work a possibility to broaden the application field of CWO crystals have been investigated by improvement of their spectrometric quality and decreasing of their afterglow level. CWO crystals with improved characteristics have been obtained (resolution for sup 1 sup 3 sup 7 Cs <8%, afterglow <0.02% after 20 ms). A possibility is considered to use these crystals for spectrometry of thermal and resonance neutrons, which is possible due to the presence of nuclei with large cross-section for these neutrons in the crystal lattice. Compounds of a new type based on Cd, La-containing double tungstates doped with rare earth elements have been synthesized, and their luminescent characteristics have been studied. ...

  13. Material and detector properties of cadmium manganese telluride (Cd1-xMnxTe) crystals grown by the modified floating-zone method

    Science.gov (United States)

    Hossain, A.; Gu, G. D.; Bolotnikov, A. E.; Camarda, G. S.; Cui, Y.; Roy, U. N.; Yang, G.; Liu, T.; Zhong, R.; Schneeloch, J.; James, R. B.

    2015-06-01

    We demonstrated the material- and radiation-detection properties of cadmium manganese telluride (Cd1-xMnxTe; x=0.06), a wide-band-gap semiconductor crystal grown by the modified floating-zone method. We investigated the presence of various bulk defects, such as Te inclusions, twins, and dislocations of several as-grown indium-doped Cd1-xMnxTe crystals using different techniques, viz., IR transmission microscopy, and chemical etching. We then fabricated four planar detectors from selected CdMnTe crystals, characterized their electrical properties, and tested their performance as room-temperature X- and gamma-ray detectors. Our experimental results show that CMT crystals grown by the modified floating zone method apparently are free from Te inclusions. However, we still need to optimize our growth parameters to attain high-resistivity, large-volume single-crystal CdMnTe.

  14. Luminescence of Single Crystals Cadmium Bromide Doped with Impurities of Argentum

    Directory of Open Access Journals (Sweden)

    N.V. Stetsyk

    2014-06-01

    Full Text Available Temperature behaviors of X-ray luminescence (XL or RL, photoluminescence (PL, and thermoluminescence (TL were studied in CdBr2 : Ag+ single crystals from room temperature to liquid nitrogen temperature. The luminescence is practically absent in the interband (including X-rays excitation crystals CdBr2 : Ag+, but manifested in the excitation light from the region 3.68 eV. In this region of the spectrum selective absorption band of silver impurity centers is observed. It was found that the crystals CdBr2 : Ag+ are sensitive to the action of X-rays and ultraviolet light through the flow of photochemical reactions (FHR in these crystals.

  15. Synthesis, crystal structure and optical properties of two new layered cadmium iodates: Cd(IO3)X (X=Cl, OH)

    International Nuclear Information System (INIS)

    Systematic explorations of new compounds in the cadmium iodate system by hydrothermal reactions led to two layered iodates, namely, Cd(IO3)X (X=Cl, OH). Cd(IO3)Cl crystallizes in the orthorhombic space group Cmca (No. 64) whereas Cd(IO3)(OH) crystallizes in the orthorhombic space group Pnma (No. 62). Cd(IO3)Cl displays a unique double layered structure composed of 1∞[Cd−O3Cl]n chains. Cadmium octahedrons form a 1D chain along the a-axis through edge sharing, and such chains are further interconnected via IO3 groups to form a special double layer on (020) plane. Cd(IO3)(OH) also exhibits a layered structure that is composed of cadmium cations, IO3 groups and hydroxyl ions. Within a layer, chains of CdO6 edge-shared octahedra are observed along the b-axis. And these chains are connected by IO3 groups into a layer parallel to the bc plane. Spectroscopic characterizations, elemental analysis, and thermogravimetric analysis for the reported two compounds are also presented. - Graphical abstract: Two new layered cadmium iodates Cd(IO3)X (X=Cl, OH) are reported. Cd(IO3)Cl features a unique double layered structure whereas Cd(IO3)(OH) displays an ordinary layered structure. - Highlights: • Two new layered cadmium iodates Cd(IO3)X (X=Cl, OH) are reported. • Cd(IO3)Cl features a unique double layered structure. • Cd(IO3)(OH) displays an ordinary layered structure. • The spectroscopic and thermal properties have been studied in detail

  16. Development of radiopure cadmium tungstate crystal scintillators from enriched {sup 106}Cd and {sup 116}Cd to search for double beta decay

    Energy Technology Data Exchange (ETDEWEB)

    Danevich, F. A.; Boiko, R. S.; Chernyak, D. M.; Kobychev, V. V.; Kropivyansky, B. N.; Mokina, V. M.; Nikolaiko, A. S.; Poda, D. V.; Podviyanuk, R. B.; Tretyak, V. I. [Institute for Nuclear Research, Kyiv (Ukraine); Barabash, A. S.; Konovalov, S. I.; Umatov, V. I. [Institute of Theoretical and Experimental Physics, Moscow (Russian Federation); Belli, P.; Bernabei, R.; D' Angelo, S. [INFN, Section of Rome Tor Vergata, Rome, Italy and Department of Physics, University of Rome Tor Vergata, Rome (Italy); Brudanin, V. B. [Joint Institute for Nuclear Research, Dubna (Russian Federation); Cappella, F.; Incicchitti, A. [INFN, Section of Rome La Sapienza, Rome, Italy and Department of Physics, University of Rome La Sapienza, Rome (Italy); Caracciolo, V. [INFN, Gran Sasso National Laboratories, Assergi (Aq), Italy and Department of Physics, University of L' Aquila, L' Aquila (Italy); and others

    2013-08-08

    Cadmium tungstate crystal scintillators enriched in {sup 106}Cd up to 66% ({sup 106}CdWO{sub 4}) and in {sup 116}Cd up to 82% ({sup 116}CdWO{sub 4}) have been developed. The low radioactive contamination of the crystals measured on the level of ≤ 1.5 mBq/kg ({sup 40}K), ≤ 0.005 - 0.012 mBq/kg ({sup 226}Ra), 0.04 - 0.07 mBq/kg ({sup 228}Th) allows to carry out high sensitivity experiments to search for double beta processes in {sup 106}Cd and {sup 116}Cd.

  17. Single pot synthesis of pyridine-N-oxide based polymeric complexes of cadmium and manganese: Crystal structure and luminescence property

    Science.gov (United States)

    Mondal, Sandip; Guha, Averi; Suresh, Eringathodi; Jana, Atish Dipankar; Banerjee, Arpita

    2012-12-01

    Two new polymeric complexes of cadmium(II) and manganese(II) with Pyridine-N-oxide (pyo) mediated by thiocyanate and dicyanamide (dca) anions have been synthesized and characterized by X-ray single crystal structure analysis. The structural analyses reveal that complexes [Cd(pyo)2(SCN)2]n (1) and [Mn(pyo)2(dca)2]n (2) [where, pyo = pyridine-N-oxide; dca = dicyanamide] are 2D coordination polymers. In complex 1 hexa-coordinated Cd(II) centers posses distorted octahedral coordination environments. Each Cd(II) is coordinated by four SCN- in end to end fashion forming a zigzag chain and two pyo monodentate ligands bridge two adjacent Cd(II) centers leading to a two-dimensional sheet structure. In complex 2 hexa-coordinated Mn(II) centers posses octahedral coordination environments. The coordination polymer constitute a 2D polymeric sheet and has a (4, 4) grid network architecture Successive stacking of coordination polymeric sheets are enforced by inter layer OH⋯O and OH⋯N hydrogen bonding. The luminescence properties of these two polynuclear complexes in solid state were studied and complex 1 exhibits higher luminescence intensity than 2.

  18. Synthesis and Crystal Structure of a New 2D Honeycomb-like Cadmium(Ⅱ) Complex with Tripodal Ligand

    Institute of Scientific and Technical Information of China (English)

    SUN,Wei-Yin(孙为银); FAN,Jian(樊健); OKAMURA,Taka-aki(罔村高明); TANG,Wen-Xia(唐雯霞); UEYAMA,Norikazu(上山憲一)

    2002-01-01

    Anew cadmium(Ⅱ) coordination polymer, [Cd(TITMB)2]-(SO4) @ 21H2O, where TITMB = 1, 3, 5-tris (imidazol-1-yl-methyl)-2,4,6-trimethylbenzene, was obtained by self-assembly of tripodal ligand TITMB with CdSO4@2.7H2O in acetonitrile,and characterized by X-ray crystallography. The crystal data belongs to monoclinic space group Cc with cell parameters a =1.16891(4) nm, b =2.06671(6) nm, c =2.48185(7) nm, β=97.8560(10)°, R = 0.0487, wR = 0.1211. The results of structure analysis indicate that each TITMB ligand coordinates three metal atoms and in turn each Cd(Ⅱ) atom with octahedral coordination geometry connects six nitrogen atoms of imidazole group from six different TITMB ligands to produce a 2D honeycomb network structure. There are a lot of water molecules linked by hydrogen bonds and occupied the channels formed intra- and inter-sheets.

  19. Photocatalytic hydrogen evolution with platinum loaded cadmium-iron-sulfide mixed crystal powders in aqueous media

    International Nuclear Information System (INIS)

    Mixed crystal powders based on Cd, Fe, and S have been synthesized by varying the ratio of CdS and FeS2 in order to find a suitable material useful for the effective conversion of solar energy. Hydrogen gas was evolved only with CdS/Pt by photocatalytic reaction under white light in an aqueous 1 M sodium sulfite solution. From electrochemical studies of semiconductor electrodes, it was shown that the onset potential shifted to the positive direction and that the bandgap energy also decreased as the molar ratio of Fe increased. A hydrogen evolution mechanism in terms of the conduction band potential and hydrogen evolution potential is proposed

  20. Electronic Band Structure and Optical Characteristics of Quantum-Size Cadmium Telluride Crystals in Glass Films

    Science.gov (United States)

    Potter, Barrett George, Jr.

    Low-dimensional semiconductor structures now occupy a position of central importance with regard to the understanding and application of the basic physics of quantum confinement. Isolated II-VI semiconductor crystals embedded in transparent, insulating matrices represent a convenient medium for the study of quantum-size effects on the electronic and optical properties of compound semiconductors. The present study simultaneously examines finite crystal size-related shifts in the energies of optical transitions originating from states located at two different critical points of the zincblende Brillouin zone of CdTe. Using a versatile, dual source, R.F.-sputtering technique, CdTe-glass composite thin films have been produced possessing average crystal sizes ranging from 24 to 125 A in films containing 5 vol% semiconductor as determined by cross-sectional, transmission electron microscopy. Previously unattainable control over such microstructural characteristics as volume fraction and crystalline phase distribution throughout the matrix have been demonstrated using the sequential sputtering process. Analysis of quantum-size induced transition energy shifts, monitored by optical absorption, indicates the persistence of significant Coulomb interactions between carriers at the T-point of CdTe in crystallite sizes 0.3 times the size of the bulk exciton. L-point transition energy shifts support the existence of two-dimensional bound electron-hole pair states whose center-of-mass motion is confined within the potential well. The influence of finite crystal size distribution width on the interpretation of quantum confinement effects in these materials was also analyzed using a numerical integration technique. Findings substantiate the relative dominance of inhomogeneous broadening effects over homogeneous broadening in determining the observed absorption lineshape of the polydisperse collection of crystallites. This does not, however, explain an apparent saturation of the

  1. Cooperative luminescence of some trivalent lanthanide ions in cadmium fluoride crystals

    International Nuclear Information System (INIS)

    Two different trivalent lanthanide ions simultaneously introduced into CdF2 crystals often give rise to cooperative phenomena. Some pairs of Er3+, Yb3+, Tb3+, Ho3+ and Tm3+ have been studied. As in the individual fluorescence properties of each ion, the energy transfers between the pairs strongly depends on the symmetry imposed to the centres by the charge compensation. The general features of the behaviours of these Ln3+ pairs into CdF2 will be mostly given for Er3++Yb3+. Some results with other pairs will be shortly described too. (Auth.)

  2. Large-area mercuric iodide photodetectors

    International Nuclear Information System (INIS)

    This article discusses the limits of the active area of mercuric iodide photodetectors imposed by the size of available crystals, electronic noise, and the uniformity of charge carrier collection. Theoretical calculations of the photodetector electronic noise are compared with the experimental results. Different entrance contacts were studied including semitransparent palladium films and conductive liquids. HgI2 photodetectors with active area up to 4 sq cm are matched with NaI(Tl) and CsI(Tl) scintillation crystals and are evaluated as gamma radiation spectrometers

  3. Crystal structure of Helicobacter pylori neutrophil-activating protein with a di-nuclear ferroxidase center in a zinc or cadmium-bound form

    Energy Technology Data Exchange (ETDEWEB)

    Yokoyama, Hideshi, E-mail: h-yokoya@u-shizuoka-ken.ac.jp [School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526 (Japan); Tsuruta, Osamu; Akao, Naoya; Fujii, Satoshi [School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526 (Japan)

    2012-06-15

    Highlights: Black-Right-Pointing-Pointer Structures of a metal-bound Helicobacter pylori neutrophil-activating protein were determined. Black-Right-Pointing-Pointer Two zinc ions were tetrahedrally coordinated by ferroxidase center (FOC) residues. Black-Right-Pointing-Pointer Two cadmium ions were coordinated in a trigonal-bipyramidal and octahedral manner. Black-Right-Pointing-Pointer The second metal ion was more weakly coordinated than the first at the FOC. Black-Right-Pointing-Pointer A zinc ion was found in one negatively-charged pore suitable as an ion path. -- Abstract: Helicobacter pylori neutrophil-activating protein (HP-NAP) is a Dps-like iron storage protein forming a dodecameric shell, and promotes adhesion of neutrophils to endothelial cells. The crystal structure of HP-NAP in a Zn{sup 2+}- or Cd{sup 2+}-bound form reveals the binding of two zinc or two cadmium ions and their bridged water molecule at the ferroxidase center (FOC). The two zinc ions are coordinated in a tetrahedral manner to the conserved residues among HP-NAP and Dps proteins. The two cadmium ions are coordinated in a trigonal-bipyramidal and distorted octahedral manner. In both structures, the second ion is more weakly coordinated than the first. Another zinc ion is found inside of the negatively-charged threefold-related pore, which is suitable for metal ions to pass through.

  4. Investigation on structural, optical, thermal, mechanical and dielectric properties of L-proline cadmium chloride monohydrate single crystals: An efficient NLO material

    Energy Technology Data Exchange (ETDEWEB)

    Singh, Preeti; Hasmuddin, Mohd [Crystal Growth and XRD Lab, Department of Physics, Jamia Millia Islamia, New Delhi 110 025 (India); Shakir, Mohd [Crystal Growth and XRD Lab, Department of Physics, Jamia Millia Islamia, New Delhi 110 025 (India); CSIR-National Physical Laboratory, New Delhi 110 012 (India); Department of Physics, ARSD College, University of Delhi, New Delhi 110021 (India); Vijayan, N. [Department of Physics, Kakatiya University, Warangal 506 009 (India); Abdullah, M.M. [Crystal Growth and XRD Lab, Department of Physics, Jamia Millia Islamia, New Delhi 110 025 (India); Advanced Materials and Nano-research Centre (AMNC), Faculty of Science and Arts, Najran University, P.O. Box-1988, Najran 11001 (Saudi Arabia); Ganesh, V. [Department of Physics, Kakatiya University, Warangal 506 009 (India); Wahab, M.A., E-mail: aries.pre84@gmail.com [Crystal Growth and XRD Lab, Department of Physics, Jamia Millia Islamia, New Delhi 110 025 (India)

    2013-10-01

    In the present work, we have grown single crystals of L-proline cadmium chloride monohydrate (LPCCM) by slow evaporation solution technique (SEST) at room temperature and recorded their live growth kinetics with the help of inverted microscope. Crystal size at various stages of growth and its corresponding morphology was also recorded. Powder X-ray diffraction (PXRD) analysis of LPCCM single crystals confirmed the orthorhombic structure. Respective values of crystallite size, strain and dislocation density have been calculated using PXRD data. Metal complex coordination of the single crystal is studied by FTIR spectroscopic. The optical properties of the grown crystals were investigated through UV–VIS spectroscopic studies and shows that the crystals have very low absorption in entire characterized wavelength range 200–800 nm. The optical band gap was calculated and found to be ∼5.6 eV. Optical constants of the material is determined by theoretical calculations. The chemical etching study was also carried out to study the density of defects in the grown crystals. The photoluminous excitation and emission spectra and thermal property by TGA/DTA curve were recorded. Further, the mechanical properties have been studied using Vicker's microhardness tester as well as many parameters such as fracture toughness (K{sub c}), Brittleness index (B{sub i}) and yield strength (σ{sub ν}) are presented. Dielectric studies have been carried out with varying frequency and temperatures. - Highlights: • The morphology of LPCCM crystal was observed during growth under inverted microscope. • Observation also shows defects also grows with the growth of crystal. • Positive temperature coefficient is observed. • The optical study shows its suitability for photonics and optical applications.

  5. Crystal structure of (E-2-(2-{5-[(2-acetoxyethyl(methylamino]thiophen-2-yl}vinyl-3-methylbenzothiazolium iodide monohydrate

    Directory of Open Access Journals (Sweden)

    Xian-Shun Sun

    2014-10-01

    Full Text Available In the cation of the title hydrated salt, C19H21N2O2S2+·I−·H2O, the benzothiazolium ring system is approximately planar [maximum deviation = 0.0251 (15 Å], and it makes a small dihedral angle of 1.16 (18° with the plane of the thiophene ring. In the crystal, the cations, anions and crystalline water molecules are linked by classical O—H...O, O—H...I and weak C—H...O hydrogn bonds, forming a three-dimensional supramolecular network. π–π stacking is observed between parallel thiazole rings of adjacent cations [centroid–centroid distance = 3.5945 (16 Å].

  6. Europium-doped barium bromide iodide

    Energy Technology Data Exchange (ETDEWEB)

    Gundiah, Gautam; Hanrahan, Stephen M.; Hollander, Fredrick J.; Bourret-Courchesne, Edith D.

    2009-10-21

    Single crystals of Ba0.96Eu0.04BrI (barium europium bromide iodide) were grown by the Bridgman technique. The title compound adopts the ordered PbCl2 structure [Braekken (1932). Z. Kristallogr. 83, 222-282]. All atoms occupy the fourfold special positions (4c, site symmetry m) of the space group Pnma with a statistical distribution of Ba and Eu. They lie on the mirror planes, perpendicular to the b axis at y = +-0.25. Each cation is coordinated by nine anions in a tricapped trigonal prismatic arrangement.

  7. Gomphrena claussenii, a novel metal-hypertolerant bioindicator species, sequesters cadmium, but not zinc, in vacuolar oxalate crystals

    NARCIS (Netherlands)

    Villafort Carvalho, M.T.; Pongrac, P.; Mumm, R.; Arkel, van J.; Aelst, van A.; Jeromel, L.; Vavpetic, P.; Pelicon, P.; Aarts, M.G.M.

    2015-01-01

    Gomphrena claussenii is a recently described zinc (Zn)- and cadmium (Cd)-hypertolerant Amaranthaceae species displaying a metal bioindicator Zn/Cd accumulation response. We investigated the Zn and Cd distribution in stem and leaf tissues of G. claussenii at the cellular level, and determined metabol

  8. Synthesis of mercuric iodide and bismuth tri-iodide nanoparticles for heavy metal iodide films nucleation

    Energy Technology Data Exchange (ETDEWEB)

    Fornaro, L.; Pereira, H.Bentos [Compound Semiconductors Group, CURE, Universidad de la Republica, Rocha (Uruguay); Aguiar, I.; Perez Barthaburu, M. [Compound Semiconductors Group, Facultad de Quimica, Univ. de la Republica, Montevideo (Uruguay)

    2011-12-15

    We synthesized mercuric iodide and bismuth tri-iodide nanoparticles by suspension in octadecene, from Hg(NO{sub 3}){sub 2}.H{sub 2}O and I{sub 2}, and from Bi(NO{sub 3}){sub 3}.5H{sub 2}O and I{sub 2}, respectively. The best synthesis conditions were 2 h at 70-80 C, followed by 10 min at 110 C for mercuric iodide nanoparticles, and 4 h at 80-110 C, followed by 10 min at 180-210 C for bismuth tri-iodide ones. Nanoparticles were then washed and centrifuged with ether repeatedly. Compounds identity was confirmed by X-ray diffraction (XRD) and energy dispersive spectrometry (EDS). We found shifts of the X-ray diffraction maxima for nanoparticles of both compounds. We characterized the nanoparticles by transmission (TEM) and scanning (SEM) electron microscopy. We obtained disk-like and squared mercuric iodide nanostructures, 80-140 nm and 100-125 nm in size respectively. We also obtained rounded and rod-like bismuth tri-iodide nanoparticles, 30-500 nm in size. Acetonitrile and isopropanol suspensions of mercuric iodide nanoparticles, and acetonitrile suspension of bismuth tri-iodide nanoparticles exhibited peak maxima shifts in their UV-Vis spectra. We synthesized for the first time mercuric iodide and bismuth tri-iodide nanoparticles by the suspension method, although we have not yet obtained uniform shape and size distributions. They offer interesting perspectives for crystalline film nucleation and for improving current applications of these materials, as well as for opening new ones. (copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  9. 21 CFR 172.375 - Potassium iodide.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Potassium iodide. 172.375 Section 172.375 Food and... Dietary and Nutritional Additives § 172.375 Potassium iodide. The food additive potassium iodide may be safely used in accordance with the following prescribed conditions: (a) Potassium iodide may be...

  10. Synthesis and Crystal Structure of Cadmium(Ⅱ)Complex [Cd(H2O)(CH3OC6H4COO)2]n

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    At room temperature, the reaction of CdNO32@4H2O and anisic acid in an ethanol solution affords the cadmium (Ⅱ) complex [Cd(H2O)(CH3OC6H4COO)2]n. The crystal is of monoclinic, empirical formula C16H16O7Cd, Mr = 432.69, space group C2/c with parameters: a = 34.211(2), b = 6.030(2), c = 7.611(3)A, β = 95.619(5)°, V = 1562.5(9)A3, Z = 4, Dc = 1.831 g/cm3, μ = 1.434 mm-1, F000 = 856, R = 0.0215 and wR = 0.0456. 1121 reflections with I>2σ(I) were considered to be observed. Each cadmium atom is seven-coordinate in a distorted pentagonal bipyramidal geometry. The Cd (Ⅱ) center is doubly bridged with the neighboring Cd centers by anisate ligands to form a four-membered ring with a repeating unit of Cd-O-Cd-O-. The extended structure and hydrogen-bonding patterns displayed in the complex were studied.

  11. Atomic force microscopy studies on growth mechanisms and defect formations on {l_brace}110{r_brace} faces of cadmium mercury thiocyanate crystals

    Energy Technology Data Exchange (ETDEWEB)

    Jiang, X.N.; Xu, D.; Yuan, D.R.; Sun, D.L.; Lu, M.K.; Zhang, G.H.; Guo, S.Y. [Shandong Univ., Jinan, SD (China). Inst. of Crystal Materials

    2001-07-01

    Growth mechanisms and defect formations on {l_brace}110{r_brace} faces of cadmium mercury thiocyanate crystals grown at 30 C ({sigma} = 0.24) were investigated by using atomic force microscopy (AFM). It was found that, under this condition, spiral dislocation controlled mechanism and 2D nucleation mechanism operates simultaneously and equally during growth, which is completely different from the traditional 2D nucleation and dislocation source controlled mechanisms. A number of 2D nucleus are formed at the large step terraces generated by dislocation sources, leading to the unequal growth rates of the elementary steps and thereby ''step bunches'' are caused. Various defects are formed under this growth condition, which is assumed to result from the incongruence between the steps generated by different sources. A new kind of 2D defect, corresponding to one growth layer in height, was observed for the first time. (orig.)

  12. Mercuric iodide sensor technology

    International Nuclear Information System (INIS)

    This report describes the improvement in the performance and the manufacturing yield of mercuric iodide detectors achieved by identifying the dominant impurities, carrier traps, and processing steps limiting device performance. Theoretical studies of electron and hole transport in this material set fundamental limits on detector performance and provided a standard against which to compare experimental results. Spectroscopy techniques including low temperature photoluminescence and thermally stimulated current spectroscopy were applied to characterize the deep level traps in this material. Traps and defects that can be introduced into the detector during growth, from the contact, and during the various steps in detector fabrication were identified. Trap energy levels and their relative abundances were determined. Variations in material quality and detector performance at the micron scale were investigated to understand the distribution in electric field in large volume detectors suitable for gamma-ray spectroscopy. Surface aging and contact degradation was studied extensively by techniques including atomic force microscopy, transmission electron microscopy, and variable angle spectroscopic ellipsometry. Preferred handling and processing procedures for maximizing detector performance and yield were established. The manufacturing yield of high resolution gamma-ray detectors was improved from a few percent to more than 30%

  13. Cadmium carcinogenesis

    International Nuclear Information System (INIS)

    Cadmium is a heavy metal of considerable environmental and occupational concern. Cadmium compounds are classified as human carcinogens by several regulatory agencies. The most convincing data that cadmium is carcinogenic in humans comes from studies indicating occupational cadmium exposure is associated with lung cancer. Cadmium exposure has also been linked to human prostate and renal cancer, although this linkage is weaker than for lung cancer. Other target sites of cadmium carcinogenesis in humans, such as liver, pancreas and stomach, are considered equivocal. In animals, cadmium effectively induces cancers at multiple sites and by various routes. Cadmium inhalation in rats induces pulmonary adenocarcinomas, in accord with its role in human lung cancer. Cadmium can induce tumors and/or preneoplastic lesions within the rat prostate after ingestion or injection. At relatively high doses, cadmium induces benign testicular tumors in rats, but these appear to be due to early toxic lesions and loss of testicular function, rather than from a specific carcinogenic effect of cadmium. Like many other metals, cadmium salts will induce mesenchymal tumors at the site of subcutaneous (s.c.) or intramuscular (i.m.) injections, but the human relevance of these is dubious. Other targets of cadmium in rodents include the liver, adrenal, pancreas, pituitary, and hematopoietic system. With the exception of testicular tumors in rodents, the mechanisms of cadmium carcinogenesis are poorly defined. Cadmium can cause any number of molecular lesions that would be relevant to oncogenesis in various cellular model systems. Most studies indicate cadmium is poorly mutagenic and probably acts through indirect or epigenetic mechanisms, potentially including aberrant activation of oncogenes and suppression of apoptosis

  14. Synthesis and Crystal Structure of Dinuclear Cadmium Complex [Cd2(phen)4(fca)2](ClO4)2·(H2O)2

    Institute of Scientific and Technical Information of China (English)

    YANG Jia-Xiang; ZHANG Ze; WU Jie-Ying; TIAN Yu-Peng; DU Peng; LIU Qing-Liang; FUN Hoong Kun; C. Suchada

    2003-01-01

    A novel complex [Cd2(phen)4(fca)2](ClO4)2((H2O)2 (fca = dianion of 3-ferrocenyl- 2-crotonic acid, phen = 1,10-phenanthroline) has been synthesized and characterized by X-ray single-crystal structure analysis. It crystallizes in triclinic system, space group Pī with a = 11.6297(5), b = 12.5165(5), c = 13.8986(6) A, α = 63.345(1), β = 87.747(1), γ = 71.862(1)°, V = 1706.20(1) A3, Z = 1, Dc = 1.673 g/cm3, F(000) = 868 and μ(MoKα) = 1.185 mm-1 (λ = 0.71073 A). R = 0.0800 and Wr = 0.1793 for 7653 observed reflections (I > 2σ(I)). The structure consists of a dinuclear cation [Cd2(phen)4(fca)2]2+, two discrete perchlorate anions and two water molecules. The cationic part of the complex shows a tetrametallic core in which two fca groups act as the (O, O') bridging ligands between two cadmium(Ⅱ) ions with a distorted octahedral environment. The Cd…Cd intradimer distance is 4.128 A.

  15. Pendant-armed Unsymmetrical Aza-macrocycles: Syntheses,Coordination Behavior and Crystal Structure of a Dinuclear Cadmium Complex

    Institute of Scientific and Technical Information of China (English)

    TAO,Jing-Chao(陶京朝); LIAO,Xin-Cheng(廖新成); WANG,Xing-Wang(王兴旺); DU,Chen-Xia(杜晨霞)

    2002-01-01

    Two nsymmetrical tetradentate aza-macrocycles with side arms attached to the N3sp atoms, L1 and L2, as well as their complexes with different metal cations were synthesized and characterized by EA, UV, IR, 1H NMR and MS spectra. Both the two ligands can efficiently transport alkali and transition metal cations across an organic membrane with high selectivity ratio. The structure of a dinuclear Cd(Ⅱ)complex [L1@(CdCl2)2] was elucdated by X-ray crystallography and was solved by the heavy-atom method to afinal R value of 0.029 for 3084reflections with |F| >3σ(I). In the exo-structore of the dinuclear complex each cadmium atom is five-coordinated, bonding to three N atoms and two chlorine atoms.

  16. Pendant—armed Unsymmetrical Aza—macrocycles:Syntheses,Coordination Behavior and Crystal Structure of a Dinuclear Cadmium Complex

    Institute of Scientific and Technical Information of China (English)

    陶京朝; 廖新成; 等

    2002-01-01

    Two unsymmetridcal tetradentate aza-macrocycles with side arms attached to whte Nsp3 atoms ,L1 and L2 ,as well as their complexes with different metal cations were synthesized and characterized by EA,UV IR ,1H NMR and MS spectra ,Both the two ligands can efficiently transport alkai and transition metal cations across an organic membrane with high selectivity ratio.The structure of a dinuclear Cd(Ⅱ) complex [L1.(CdCl2)2] was elucidated by X-ray crystallography and was solved by the heavy-atom method to a final R value of 0.029 for 3084 reflections with |F|>3σ(I), In the exo-structure of the dinuclear complex each cadmium atom is five-coordinated,bonding to three N atoms and two chlorine atoms.

  17. Novel mercuric iodide polycrystalline nuclear particle counters

    Energy Technology Data Exchange (ETDEWEB)

    Schieber, M. [Hebrew Univ. of Jerusalem (Israel)]|[Sandia National Labs., Livermore, CA (United States); Zuck, A.; Braiman, M.; Nissenbaum, J. [Hebrew Univ. of Jerusalem (Israel); Turchetta, R.; Dulinski, W.; Husson, D.; Riester, J.L. [LEPSI, Strasbourg (France)

    1997-12-01

    Polycrystalline mercuric iodide nuclear radiation detectors have been produced in a novel technology. Unlike the normal single-crystal technology, there is no intrinsic limit to the surface on which these detectors can be produced. Detectors with areas up to about 1.5 cm{sup 2}, thicknesses from 30 to 600 {micro}m, and with single electrodes as well as microstrip and pixel contacts have been fabricated and successfully tested with photons in the range of 40--660 keV, {beta} particle`s emitted from a Sr-Y source, and high energy (100 GeV) muons. Results on both charge collection and counting efficiency are reported as well as some very preliminary imaging results. The experimental results on charge collection have been compared with simulation, and a combined {mu}{tau} product 10{sup {minus}7} cm{sup 2}/V for electrons has been estimated.

  18. 21 CFR 184.1634 - Potassium iodide.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Potassium iodide. 184.1634 Section 184.1634 Food... Specific Substances Affirmed as GRAS § 184.1634 Potassium iodide. (a) Potassium iodide (KI, CAS Reg. No. 7681-11-0) is the potassium salt of hydriodic acid. It occurs naturally in sea water and in...

  19. 21 CFR 582.5634 - Potassium iodide.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Potassium iodide. 582.5634 Section 582.5634 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Supplements 1 § 582.5634 Potassium iodide. (a) Product. Potassium iodide. (b) Tolerance. 0.01 percent....

  20. Development of high-efficiency solar cells on copper indium selenide single crystals (cadmium sulfide, zinc oxide)

    Energy Technology Data Exchange (ETDEWEB)

    Yip, Lap Sum

    1996-12-31

    Photovoltaic cells with a ZnO/CdS/CuInSe{sub 2} structure were fabricated on bulk CuInSe{sub 2} substrates. Conversion efficiencies of more than or near 10 per cent were obtained on cells with an active area and without the use of antireflection coating. Copper indium selenide single crystals can be used as absorbers in thin film solar cells. In this study, the single crystals were grown by a horizontal Bridgman method. An annealing of the CuInSe{sub 2} substrate before the CdS deposition was found to be essential in obtaining high photovoltaic performance.

  1. Synthesis and crystal structures of novel LaOAgS-type alkaline earth – Zinc, manganese, and cadmium fluoride pnictides

    Energy Technology Data Exchange (ETDEWEB)

    Charkin, Dmitri O., E-mail: charkin@inorg.chem.msu.ru; Urmanov, Arthur V.; Plokhikh, Igor V.; Korshunov, Alexander D.; Kuznetsov, Alexey N.; Kazakov, Sergey M.

    2014-02-05

    Highlights: • Sight new alkaline earth – Mn, Zn, Cd fluoride pnictides were prepared. • All new compounds adopt the LaOAgS structure type. • Bond distances in their structures are transferable within 2–3%. • Very close similarities are observed in structural chemistry of LaOAgS- and HfCuSi{sub 2}-type compounds of Mn, Cu, Zn, Ag, and Cd. -- Abstract: Systematic studies of the LaOAgS-type compounds among alkaline earth – Zn/Cd/Mn fluoride pnictides revealed the existence of new representatives SrFMnP, SrFMnAs, SrFMnSb, SrFZnAs, SrFZnSb, BaFZnAs, BaFCdP, and BaFCdAs. Similar to rare-earth oxide compounds and contrary to isolobal chalcogenides of Cu/Ag, not all possible compositions could be realized. No compound of the structure type is formed for calcium; strontium forms fluoride pnictides only with zinc and manganese, while for barium, new representatives are also formed with cadmium. This trend, which possibly has a geometrical origin, is corroborated by quantum chemical calculations. Formation of NdOZnP-type compounds also was not observed suggesting the structure to be characteristic only for rare earth – zinc oxide phosphides.

  2. Crystal growth and analysis of ohmic contact and magneto-optical isolator properties of cadmium manganese telluride

    Science.gov (United States)

    Prakasam, Mythili; Viraphong, Oudomsack; Teulé-Gay, Lionel; Decourt, Rodolphe; Veber, Philippe; Víllora, Encarnación G.; Shimamura, Kiyoshi

    2011-03-01

    Cd1-xMnxTe (x=0.1, 0.3, 0.5, 0.7 and 0.9) (CMT) single crystals were grown by the vertical Bridgman method. The optical studies reveal that with the increase in Mn concentration, the band gap values increase, which is attributed to s, p-d exchange interaction between the band carriers and Mn ions. Faraday rotation angle of the grown CMT (x=0.5) crystals were measured at the following wavelengths: 825, 1060 and 1575 nm. It was inferred that CMT exhibit larger Faraday effect (3-6 times larger than terbium-gallium garnet (TGG) currently used for optical isolators) making it as an efficient material for optical isolator at longer wavelengths. Field-cooled and zero field-cooled magnetizations of CMT were measured as a function of temperature and magnetic field. The spin-glass like behavior of CMT and their tendency to decrease in magnitude with increasing Mn concentration have been analyzed. The metal contacts on the Cd1-xMnxTe (x=0.1, 0.5, 0.7 and 0.9) crystals have been made with various metals and metal alloys to establish the ohmic contact. The detector characteristics of CMT have been tested using γ-rays with 511 keV (22 Na) and 59.5 keV (241 Am).

  3. Antifungal activity of nicotine and its cadmium complex

    International Nuclear Information System (INIS)

    Nicotine and its metal complex; Cd(II)-nicotine were isolated from leaves of Nicotiana tabacum using various metal ions by the reported techniques and studied for their antifungal activities against fourteen different species of fungi. For comparative study, pure sample of nicotine and metal salt used for complexation; cadmium(II) iodide was also subjected to antifungal tests with the same species of fungus under similar conditions. Results indicated that nicotine is quite effective against the rare pathogenic and Non pathogenic fungi but comparatively less effective against Pathogenic fungi. Nicotine was found to be completely ineffective against the selected species of Occasional pathogenic fungi. Cadmium(II) iodide effectively inhibited Pathogenic and Non pathogenic fungi whereas relatively ineffective against the Occasional pathogenic and Rare pathogenic fungi. On the other hand, Cadmium(II) nicotine complex inhibited all the selected species of fungi except Fusarium solani. (author)

  4. 半导体激光倍频晶体硫氰酸汞镉(CMTC)显微结晶的研究%Study on Micro-crystallization of Cadmium Mercury Thiocyanate (CMTC) Crystal for Laser Diode Frequency Doubling

    Institute of Scientific and Technical Information of China (English)

    袁多荣; 钟真武; 张吉果; 段秀兰; 郭世义; 王新强; 姜雪宁; 许东; 吕孟凯; 方奇

    2001-01-01

    Crystallization behavior and habits of cadmium mercury thiocyanate (CMTC) crystal for laser diode frequency doubling in KCl/H2O solvent systems with different KCl concentrations were observed and investigated by means of micro-crystallization experiments.The results show that CMTC crystal exhibits regular crystalline morphologies,homogenous growth speed in different directions and is transparent when the concentration of KCl ranges from 3%-10% and pH value ranges from 3.0-4.3.When pH value ranges from 2.0-3.0,the growth speed along z-axis direction increases and along a-axis direction decreases.Impurities influence greatly crystalline quality and morphology.With time passing and temperature increasing the stability of solution becomes poor.Suitable solution conditions and key factors for CMTC crystal growth and oriented growth were put forward.%采用显微结晶,系统地观察、研究了半导体激光(LD)倍频材料CMTC晶体在KCl/H2O的溶剂体系中,不同条件下的结晶习性。结果给出:在KCl浓度为3%~10%范围,pH值为3.0~4.3范围时,结晶形态规则,各项生长速度均匀,结晶透明;pH值为2.0~3.0条件下,z轴方向生长速度变快,a轴方向生长速度变慢;杂质严重影响了结晶的质量和外形;溶液稳定性随时间的增长和温度的升高而逐渐变差。本文分析了CMTC单晶生长和定向生长适宜的溶液条件和关键。

  5. Chloride, bromide and iodide scintillators with europium

    Energy Technology Data Exchange (ETDEWEB)

    Zhuravleva, Mariya; Yang, Kan

    2016-09-27

    A halide scintillator material is disclosed where the halide may comprise chloride, bromide or iodide. The material is single-crystalline and has a composition of the general formula ABX.sub.3 where A is an alkali, B is an alkali earth and X is a halide which general composition was investigated. In particular, crystals of the formula ACa.sub.1-yEu.sub.yI.sub.3 where A=K, Rb and Cs were formed as well as crystals of the formula CsA.sub.1-yEu.sub.yX.sub.3 (where A=Ca, Sr, Ba, or a combination thereof and X=Cl, Br or I or a combination thereof) with divalent Europium doping where 0.ltoreq.y.ltoreq.1, and more particularly Eu doping has been studied at one to ten mol %. The disclosed scintillator materials are suitable for making scintillation detectors used in applications such as medical imaging and homeland security.

  6. Synthesis, Characterization and Crystal Structure Determination of a Thiocyanato Bridged One-dimensional Polymeric Complex of Cadmium(Ⅱ)

    Institute of Scientific and Technical Information of China (English)

    BAI Yan; PAN Xiao-Jing; DANG Dong-Bin; SHANG Wei-Li; WANG Jing-Ping

    2008-01-01

    A new one-dimensional polymeric complex [Cd(SCN)2(H2O)]L (L = N,N'-bis(furan-2-ylmethylene)hydrazine) has been synthesized and characterized by IR, UV spectra, TG-DTA technique and single-crystal X-ray diffraction analysis. It crystallizes in triclinic, pace group P1 with a = 5.9268(8), b = 10.8678(15), c = 13.3671(19) A, α = 109.295(2), β = 95.092(2), γ =97.8580(10)°, V - 796.70(19) A3, Z = 2, C12H10CdN4O3S2, Mr = 434.76, μ = 1.648 mm-1, Dc = 1.812 g/cm3, F(000) = 428, R = 0.0308 and wR = 0.0769. The crystal structure reveals that the structure of [Cd(SCN)E(H2O)]n features di-μ-1,3-thiocyante bridges and 1D chains. The octahedrally coordinated Cd atom is surrounded by one oxygen atom from water molecule, three S atoms and two N atoms from five di-μ-1,3 thiocyanato bridges. The Cd atoms are connected by two di-μ-1,3 thiocyanato bridges with the Cd(1)…Cd(1A) separation of 4.239(1) (A) and Cd(1)…Cd(1B) of 5.852(1)(A). In addition, the one-dimensional straight chain structure is further connected by multiform intermolicular N-H…O hydrogen bonds and π…π interactions to form a three-dimensional supramolecular structure.

  7. (1,2-Dicarba-closo-dodecaboranyltrimethylmethanaminium iodide

    Directory of Open Access Journals (Sweden)

    Jong-Dae Lee

    2011-08-01

    Full Text Available The title compound, [1-(CH33NCH2-1,2-C2B10H11]+·I− or C6H22B10N+·I−, was obtained by the reaction of (1,2-dicarba-closo-dodecaboranyldimethylmethanamine with methyl iodide. The asymmetric unit contains two iodide anions and two (o-carboranyltetramethylammonium cations. The bond lengths and angles in the carborane cage are within normal ranges, but the N—Cmethylene—Ccage angle is very large [120.2 (2°] because of repulsion between the carborane and tetramethylammonium units. In the crystal, ions are linked through C—H...I hydrogen bonds.

  8. Uptake of iodide in the marine haptophyte Isochrysis sp. (T.ISO) driven by iodide oxidation.

    Science.gov (United States)

    van Bergeijk, Stef A; Hernández Javier, Laura; Heyland, Andreas; Manchado, Manuel; Pedro Cañavate, José

    2013-08-01

    Uptake of iodide was studied in the marine microalga Isochrysis sp. (isol. Haines, T.ISO) during short-term incubations with radioactive iodide ((125) I(-) ). Typical inhibitors of the sodium/iodide symporter (NIS) did not inhibit iodide uptake, suggesting that iodide is not taken up through this transport protein, as is the case in most vertebrate animals. Oxidation of iodide was found to be an essential step for its uptake by T.ISO and it seemed likely that hypoiodous acid (HOI) was the form of iodine taken up. Uptake of iodide was inhibited by the addition of thiourea and of other reducing agents, like L-ascorbic acid, L-glutathione and L-cysteine and increased after the addition of oxidized forms of the transition metals Fe and Mn. The simultaneous addition of both hydrogen peroxide (H2 O2 ) and a known iodide-oxidizing myeloperoxidase (MPO) significantly increased iodine uptake, but the addition of H2 O2 or MPO separately, had no effect on uptake. This confirms the observation that iodide is oxidized prior to uptake, but it puts into doubt the involvement of H2 O2 excretion and membrane-bound or extracellular haloperoxidase activity of T.ISO. The increase of iodide uptake by T.ISO upon Fe(III) addition suggests the nonenzymatic oxidation of iodide by Fe(III) in a redox reaction and subsequent influx of HOI. This is the first report on the mechanism of iodide uptake in a marine microalga.

  9. Rare, severe hypersensitivity reaction to potassium iodide

    DEFF Research Database (Denmark)

    Nielsen, Anne Sofie Korsholm; Ebbehøj, Eva; Richelsen, Bjørn

    2014-01-01

    The literature reports a large variety of adverse reactions to potassium iodide. A severe hypersensitivity reaction to potassium iodide in a 51-year-old woman with Graves' thyrotoxicosis is described. Following administration the patient developed sialadenitis, conjunctivitis, stomatitis and acne...

  10. Lead iodide X-ray and gamma-ray spectrometers for room and high temperature operation

    Energy Technology Data Exchange (ETDEWEB)

    Hermon, H.; James, R.B.; Cross, E. [and others

    1997-02-01

    In this study, we report on the results of the investigation of lead iodide material properties. The effectiveness of zone refining purification methods on the material purity is determined by ICP-MS and ICP-OES and correlated to the electrical and physical material properties. We show that this zone refining method is very efficient in removing impurities from lead iodide and we also determine the segregation coefficient for some of these impurities. Triple axis x- ray diffraction (TAD) analysis has been used to determine the crystalline perfection of the lead iodide after applying various cutting, etching, and fabrication methods. The soft lead iodide crystal was found to be damaged when cleaved by a razor blade, but by using a diamond wheel saw, followed by etching, the crystallinity of the material was improved, as observed by TAD. Low temperature photoluminescence also indicates an improvement in the material properties of the purified lead iodide. Electrical properties of lead iodide such as carrier mobility, were calculated based on carrier- phonon scattering. The results for the electrical properties were in good agreement with the experimental data.

  11. The effect of elemental and hydrocarbon impurities on mercuric iodide gamma ray detector performance

    Science.gov (United States)

    Cross, Eilene S.; Buffleben, George; Soria, Ed; James, Ralph; Schieber, Michael; Natarajan, Raj; Gerrish, Vern

    Mercuric iodide is a room temperature semiconductor material that is used for gamma ray and x-ray radiation detection. Mercuric iodide is synthesized from mercuric chloride and potassium iodide and is then purified by a series of melts and sublimation steps and by zone refining. The mercuric iodide is grown into crystals and platelets and then fabricated into detectors. Elemental contamination may be a determining factor in the performance of these detectors. These contaminates may be present in the starting material or may be introduced during, or be unaffected by, the purification, growth or fabrication steps. Methods have been developed for the analysis of trace levels of elemental contamination. Inductively Coupled Plasma/Mass Spectroscopy (ICP/MS), Inductively Coupled Plasma/Optical Emission Spectroscopy (ICP/OES) and Gas Chromatography/Mass Spectroscopy (GC/MS) are used to determine sub ppm levels of many trace elemental impurities. Trace levels of many elemental impurities in the raw mercuric iodide are significantly reduced during the purification and zone refining processes. Though the levels of impurities are reduced, poor performing mercuric iodide detectors have contamination levels remaining or reintroduced which are higher for Ag, Al, Ca, Cu, Mg, Mn, Na, Pb and Zn than detectors with good gamma ray response. This paper will discuss the analytical methodology, the effects of purification on impurity levels, and the correlation between detector performance and impurity levels.

  12. Mechanochromic and thermochromic luminescence of a copper iodide cluster.

    Science.gov (United States)

    Perruchas, Sandrine; Le Goff, Xavier F; Maron, Sébastien; Maurin, Isabelle; Guillen, François; Garcia, Alain; Gacoin, Thierry; Boilot, Jean-Pierre

    2010-08-18

    The mechanochromic and thermochromic luminescence properties of a molecular copper(I) iodide cluster formulated [Cu(4)I(4)(PPh(2)(CH(2)CH=CH(2)))(4)] are reported. Upon mechanical grinding in a mortar, its solid-state emission properties are drastically modified as well as its thermochromic behavior. This reversible phenomenon has been attributed to distortions in the crystal packing leading to modifications of the intermolecular interactions and thus of the [Cu(4)I(4)] cluster core geometry. Notably, modification of the Cu-Cu interactions seems to be involved in this phenomenon directly affecting the emissive properties of the cluster. PMID:20698644

  13. Predissociation dynamics of lithium iodide

    CERN Document Server

    Schmidt, H; Stienkemeier, F; Bogomolov, A S; Baklanov, A V; Reich, D M; Skomorowski, W; Koch, C P; Mudrich, M

    2015-01-01

    The predissociation dynamics of lithium iodide (LiI) in the first excited A-state is investigated for molecules in the gas phase and embedded in helium nanodroplets, using femtosecond pump-probe photoionization spectroscopy. In the gas phase, the transient Li+ and LiI+ ion signals feature damped oscillations due to the excitation and decay of a vibrational wave packet. Based on high-level ab initio calculations of the electronic structure of LiI and simulations of the wave packet dynamics, the exponential signal decay is found to result from predissociation predominantly at the lowest avoided X-A potential curve crossing, for which we infer a coupling constant V=650(20) reciprocal cm. The lack of a pump-probe delay dependence for the case of LiI embedded in helium nanodroplets indicates fast droplet-induced relaxation of the vibrational excitation.

  14. Predissociation dynamics of lithium iodide

    Energy Technology Data Exchange (ETDEWEB)

    Schmidt, H.; Vangerow, J. von; Stienkemeier, F.; Mudrich, M., E-mail: mudrich@physik.uni-freiburg.de [Physikalisches Institut, Universität Freiburg, 79104 Freiburg (Germany); Bogomolov, A. S. [Institute of Chemical Kinetics and Combustion, Novosibirsk 630090 (Russian Federation); Baklanov, A. V. [Institute of Chemical Kinetics and Combustion, Novosibirsk 630090 (Russian Federation); Novosibirsk State University, Novosibirsk 630090 (Russian Federation); Reich, D. M.; Skomorowski, W.; Koch, C. P. [Theoretische Physik, Universität Kassel, Heinrich-Plett-Str. 40, 34132 Kassel (Germany)

    2015-01-28

    The predissociation dynamics of lithium iodide (LiI) in the first excited A-state is investigated for molecules in the gas phase and embedded in helium nanodroplets, using femtosecond pump-probe photoionization spectroscopy. In the gas phase, the transient Li{sup +} and LiI{sup +} ion signals feature damped oscillations due to the excitation and decay of a vibrational wave packet. Based on high-level ab initio calculations of the electronic structure of LiI and simulations of the wave packet dynamics, the exponential signal decay is found to result from predissociation predominantly at the lowest avoided X-A potential curve crossing, for which we infer a coupling constant V{sub XA} = 650(20) cm{sup −1}. The lack of a pump-probe delay dependence for the case of LiI embedded in helium nanodroplets indicates fast droplet-induced relaxation of the vibrational excitation.

  15. Evaluation of mercuric iodide ceramic semiconductor detectors

    Energy Technology Data Exchange (ETDEWEB)

    Schieber, M.; Zuck, A.; Braiman, M.; Nissenbaum, J. [Hebrew Univ., Jerusalem (Israel); Turchetta, R.; Dulinski, W.; Husson, D.; Riester, J.L. [LEPSI (ULP/IN2P3), Strasbourg (France)

    1998-02-01

    Mercuric iodide ceramic radiation detectors, which can act as nuclear particle counters, have been fabricated with single continuos electrical contacts and with linear strip contacts. They have been tested with different kinds of {gamma} and {beta} sources as well as in a high energy beam at CERN. The detectors were also successfully tested for radiation hardness with irradiation of 5*10{sup 14} neutrons/cm{sup 2}. The ratio of detected photons over the number of absorbed photons has been measured with {gamma} sources of different energies, and it ranges from 20% at 44 keV up to about 30% at 660 keV. An absolute efficiency of 70% has been measured for a 350 {mu}m thick detector for {beta} particles emitted by a {sup 90}Sr source. Charge collection efficiency, defined as the amount of charge induced on the electrodes by a mminimum ionizing particle (MIP) traversing the detector, has been measured in two samples. The average collected charge fits well with a linear curve with slope of 35 electrons/(kV/cm) per 100 {mu}m. This result is well described by a dynamic device simulation, where the free carrier mean lifetime is used as a free parameter, adjusted to a value of 1.5 ns, i.e. about 1/100 of the corresponding lifetime in single crystal HgI{sub 2} detectors. The response to MIP has also been studied with a high energy (100 GeV) muon beam in CERN. A preliminary beam profile is presented while a more detailed analysis is still in progress and will be presented elsewhere. These results together with the low cost of the material make ceramic HgI{sub 2} detectors excellent candidates for large area particle tracking and imaging applications, even in a radiation harsh environment. (orig.). 14 refs.

  16. Plasma etching of cesium iodide

    International Nuclear Information System (INIS)

    Thick films of cesium iodide (CsI) are often used to convert x-ray images into visible light. Spreading of the visible light within CsI, however, reduces the resolution of the resulting image. Anisotropic etching of the CsI film into an array of micropixels can improve the image resolution by confining light within each pixel. The etching process uses a high-density inductively coupled plasma to pattern CsI samples held by a heated, rf-biased chuck. Fluorine-containing gases such as CF4 are found to enhance the etch rate by an order of magnitude compared to Ar+ sputtering alone. Without inert-gas ion bombardment, however, the CF4 etch becomes self-limited within a few microns of depth due to the blanket deposition of a passivation layer. Using CF4+Ar continuously removes this layer from the lateral surfaces, but the formation of a thick passivation layer on the unbombarded sidewalls of etched features is observed by scanning electron microscopy. At a substrate temperature of 220 deg. C, the minimum ion-bombardment energy for etching is Ei∼50 eV, and the rate depends on Ei1/2 above 65 eV. In dilute mixtures of CF4 and Ar, the etch rate is proportional to the gas-phase density of atomic fluorine. Above 50% CF4, however, the rate decreases, indicating the onset of net surface polymer deposition. These observations suggest that anisotropy is obtained through the ion-enhanced inhibitor etching mechanism. Etching exhibits an Arrhenius-type behavior in which the etch rate increases from ∼40 nm/min at 40 deg. C to 380 nm/min at 330 deg. C. The temperature dependence corresponds to an activation energy of 0.13±0.01 eV. This activation energy is consistent with the electronic sputtering mechanism for alkali halides

  17. Synthesis, X-ray crystal structure, optical properties and DFT studies of a new 2D layered iodide bridged Pb(II) coordination polymer with 2,3-bis(2-pyridyl)pyrazine

    Energy Technology Data Exchange (ETDEWEB)

    Saghatforoush, Lotfali, E-mail: saghatforoush@gmail.com; Bakhtiari, Akbar; Gheleji, Hojjat

    2015-01-15

    The synthesis of two dimensional (2D) coordination polymer [Pb{sub 2}(µ-I){sub 2}(µ-dpp-N,N,N,N)(µ-dpp-N,N)I{sub 2}]{sub n} (dpp=2,3-bis(2-pyridyl)pyrazine) is reported. As determined by X-ray diffraction of a twinned crystal, the dpp ligand simultaneously adopts a bis–bidentate and bis–monodentate coordination mode in the crystal structure of compound. The electronic band structure along with density of states (DOS) calculated by the DFT method indicates that the compound is an indirect band gap semiconductor. According to the DFT calculations, the observed emission of the compound at 600 nm in solid phase could be attributed to arise from an excited LLCT state (dpp-π{sup ⁎} [C-2p and N-2p states, CBs] to I-6p state [VBs]). The linear optical properties of the compound are also calculated by DFT method. The structure of the compound in solution phase is discussed based on the measured {sup 1}H NMR and fluorescence spectra in DMSO. TGA studies indicate that the compound is thermally stable up to 210 °C. - Graphical abstract: The synthesis, crystal structure and emission spectra of [Pb{sub 2}(µ-I){sub 2}(µ-dpp-N,N,N,N)(µ-dpp-N,N)I{sub 2}]{sub n} is presented. The electronic band structure and linear optical properties of the compound are calculated by the DFT method. - Highlights: • Two dimensional [Pb{sub 2}(µ-I){sub 2}(µ-dpp-N,N,N,N)(µ-dpp-N,N)I{sub 2}]{sub n} has been prepared. • The structure of the compound is determined by XRD of a twinned crystal. • DFT calculations indicate that the compound is an indirect band gap semiconductor. • As shown by DFT calculations, the emission band of the compound is LLCT. • Solution phase structure of compound is explored by {sup 1}H NMR and emission spectra.

  18. Modeling of ultrafast THz interactions in molecular crystals

    DEFF Research Database (Denmark)

    Pedersen, Pernille Klarskov; Clark, Stewart J.; Jepsen, Peter Uhd

    2014-01-01

    In this paper we present a numerical study of terahertz pulses interacting with crystals of cesium iodide. We model the molecular dynamics of the cesium iodide crystals with the Density Functional Theory software CASTEP, where ultrafast terahertz pulses are implemented to the CASTEP software...... to interact with molecular crystals. We investigate the molecular dynamics of cesium iodide crystals when interacting with realistic terahertz pulses of field strengths from 0 to 50 MV/cm. We find nonlinearities in the response of the CsI crystals at field strengths higher than 10 MV/cm....

  19. Synthesis, Crystal Structure and Properties of Iodide and Hexafluorophosphate Salts of 2-Ferrocenyl (or Binuclear Ferrocenyl)- 1,3-dialkylbenzimidazolium%2-单核和双核茂铁基-1,3-二烷基苯并咪唑盐的合成、结构及性质研究

    Institute of Scientific and Technical Information of China (English)

    王静; 冯丽敏; 马飞娟; 林芬; 谢莉莉; 袁耀锋

    2012-01-01

    Iodide salt 4 and hexafluorophosphate salt 5 of l-methyl-2-ferrocenyl-3-ethylbenzimidazolium are prepared using 2-ferrocenylbenzimidazole 2 as starting material. 2-[r-(2-Ferrocenylpropan-2-yl)ferrocen-l-yl]benzimidazole (7) is obtained by the reaction of formyl 2,2-diferrocenylpropane with o-diaminobenzene in the condition of methanol as solvent, reflux and catalysis of iodine. Iodide salt 9 and hexafluorophosphate salt 10 of l-methyl-2-[1'-(2-ferrocenylpropan-2-yl)-ferrocen-l-yl]-3-ethylbenzimidazolium are synthesized using 7 as starting material. Oxidative potentials of ferrocenyl connected directly to benzimidazolium in these salts move to more positive position to a large extent. Crystal structure of 4 is explained and n-n stacking is showed. UV-Vis spectra shows that photoinduced charge transfer exists for salts. Iodide salt 4 presents good catalytic effect on decomposition of ammonium perchlorate (AP) in DSC-TG (differential scanning calorimetry- thermogravimet-ric) test.%以2-二茂铁基苯并咪唑(2)为原料,合成了1-甲基-2-二茂铁基-3-乙基苯并咪唑碘盐(4)和六氟磷酸盐(5);甲酰化的2,2-双二茂铁基丙烷(6)与邻苯二胺在甲醇作溶剂,回流,碘催化下反应,得到2-[1’-(2-二茂铁基丙烷-2-基)二茂铁-1-基]苯并咪唑(7),以7为原料合成了1-甲基-2-[1’-(2-二茂铁基丙烷-2-基)二茂铁-1-基]-3-乙基苯并咪唑碘盐(9)和六氟磷酸盐(10).电化学分析表明所得的盐化合物中,与苯并咪唑阳离子直接相连的二茂铁的氧化电位相对2和7均产生了较大正移.对化合物4的单晶结构进行了解析,晶体结构中存在π-π堆积.UV-Vis吸收光谱表明所得盐化合物具有光致电荷迁移现象.DSC-TG(差示扫描量热-热重)测试表明碘盐4对高氯酸铵(AP)热分解有较好催化效果.

  20. Flame atomic absorption spectrometric determination of trace quantities of cadmium in water samples after cloud point extraction in Triton X-114 without added chelating agents

    Energy Technology Data Exchange (ETDEWEB)

    Afkhami, Abbas [Department of Chemistry, Faculty of Science, Bu-Ali Sina University, Hamadan (Iran, Islamic Republic of)]. E-mail: afkhami@basu.ac.ir; Madrakian, Tayyebeh [Department of Chemistry, Faculty of Science, Bu-Ali Sina University, Hamadan (Iran, Islamic Republic of); Siampour, Hajar [Department of Chemistry, Faculty of Science, Bu-Ali Sina University, Hamadan (Iran, Islamic Republic of)

    2006-11-16

    A new micell-mediated phase separation method for preconcentration of ultra-trace quantities of cadmium as a prior step to its determination by flame atomic absorption spectrometry has been developed. The method is based on the cloud point extraction (CPE) of cadmium in iodide media with Triton X-114 in the absence of any chelating agent. The optimal extraction and reaction conditions (e.g., acid concentration, iodide concentration, effect of time) were studied, and the analytical characteristics of the method (e.g., limit of detection, linear range, preconcentration, and improvement factors) were obtained. Linearity was obeyed in the range of 3-300 ng mL{sup -1} of cadmium. The detection limit of the method is 1.0 ng mL{sup -1} of cadmium. The interference effect of some anions and cations was also tested. The method was applied to the determination of cadmium in tap water, waste water, and sea water samples.

  1. Polymorphic copper iodide clusters: insights into the mechanochromic luminescence properties.

    Science.gov (United States)

    Benito, Quentin; Le Goff, Xavier F; Maron, Sébastien; Fargues, Alexandre; Garcia, Alain; Martineau, Charlotte; Taulelle, Francis; Kahlal, Samia; Gacoin, Thierry; Boilot, Jean-Pierre; Perruchas, Sandrine

    2014-08-13

    An in-depth study of mechanochromic and thermochromic luminescent copper iodide clusters exhibiting structural polymorphism is reported and gives new insights into the origin of the mechanochromic luminescence properties. The two different crystalline polymorphs exhibit distinct luminescence properties with one being green emissive and the other one being yellow emissive. Upon mechanical grinding, only one of the polymorphs exhibits great modification of its emission from green to yellow. Interestingly, the photophysical properties of the resulting partially amorphous crushed compound are closed to those of the other yellow polymorph. Comparative structural and optical analyses of the different phases including a solution of clusters permit us to establish a correlation between the Cu-Cu bond distances and the luminescence properties. In addition, the local structure of the [Cu4I4P4] cluster cores has been probed by (31)P and (65)Cu solid-state NMR analysis, which readily indicates that the grinding process modifies the phosphorus and copper atoms environments. The mechanochromic phenomenon is thus explained by the disruption of the crystal packing within intermolecular interactions inducing shortening of the Cu-Cu bond distances in the [Cu4I4] cluster core and eventually modification of the emissive state. These results definitely establish the role of cuprophilic interactions in the mechanochromism of copper iodide clusters. More generally, this study constitutes a step further into the understanding of the mechanism involved in the mechanochromic luminescent properties of metal-based compounds. PMID:25076411

  2. Nonradiometric and radiometric testing of radioiodine sorbents using methyl iodide

    International Nuclear Information System (INIS)

    A nonradiometric test of adsorbents and adsorbers with normal methyl iodide (CH3127I) is desirable. Use of methyl radioiodide (CH3131I) requires special precautions and facilities and results in bed contamination. However, first it must be established to what extent the removal of CH3127I by adsorbents is indicative of the removal of CH3131I. An experimental apparatus was built and used to simultaneously measure the penetrations of CH3I molecules and the radioisotope in CH3131I through charcoal absorbent beds. Gas chromatography with electron capture detection was used to measure CH3I. Radioiodine was measured using charcoal traps within NaI scintillation well crystals. Real time (5-min interval) radioiodine measurement provided immediate penetration results directly comparable to the real time penetrations of methyl iodide. These penetrations were compared for typical charcoal adsorbents with these impregnants: (a) 5% KI3, (b) 5% KI3 + 2% TEDA, (c) 5% TEDA, and (d) metal salts (Whetlerite). Differences between CH3I and CH3131I penetrations observed for the two iodized charcoals were attributed to isotope exchange reactions. Equivalent penetrations were observed for non-iodized adsorbents and for iodized ones at initial time. First order rates were confirmed for reactions with TEDA and for isotope exchange. This was one more confirmation of the lack of a challenge concentration effect on efficiencies at low test bed loadings. In addition to other removal mechanisms, reversible physical adsorption was observed with all charcoals

  3. The partitioning of iodides into steam

    International Nuclear Information System (INIS)

    In order to estimate the likely releases of radioactive iodine during steam generator tube rupture (SGTR) faults, it is necessary to know the relevant partition coefficients as a function of temperature and solution composition. It has been suggested previously that, under SGTR fault conditions, partitioning of free or ion-paired I- into the steam may be more extensive than that for molecular HI. This report uses available information on the partitioning of iodides and other salts to provide a means of estimating the partition coefficient of the iodide ion as a function of boric acid concentration and temperature. (author)

  4. Adsorption of radioactive iodide by natural zeolites

    International Nuclear Information System (INIS)

    Two natural zeolites from Iranian deposits (clinoptilolite and natrolite) were characterized and their ability for adsorption of iodide from nuclear wastewaters was evaluated. The adsorption behavior was studied on natural and modified zeolites by γ-spectrometry using 131I as radiotracer. Adsorption isotherms and distribution coefficient (Kd) were measured. The results showed that clinoptilolite is a more promising zeolite for removal of iodide compared to natrolite. Furthermore, the adsorption was higher in silver, lead and thallium forms, whereas the lowest desorption was observed in lead modified zeolite. (author)

  5. Bismuth tri-iodide radiation detector development

    Science.gov (United States)

    Gokhale, Sasmit S.

    Bismuth tri-iodide is an attractive material for room temperature radiation detection. BiI3 demonstrates a number of properties that are apt for semiconductor radiation detection, especially gamma ray spectroscopy. The high atomic number (ZBi = 83 and ZI = 53) and the relatively high density (5.78 g/cm3) cause the material to have good photon stopping power, while the large band-gap (1.67 eV ) allows it to function as a room temperature radiation detector without any cooling mechanism. This work presents the fabrication and characterization of BiI3 radiation detectors. For the purpose of this research detectors were fabricated by cutting BiI3 crystal boules, followed by mechanical and chemical surface treatments. Detectors with various electrode geometries enabling single polarity charge sensing were fabricated. The electrical characteristics and the radiation response of the detectors were measured. The radiation response measurement was performed at room temperature using a 241Am alpha particle source and a 241Am sealed gamma-ray source. The spectral resolutions of the detectors varied from 2.09% - 6.1% for 59.5 keV gamma-rays and between 26% - 40% for 5.48 MeV alpha particles. Charge carrier properties such as the electron and hole mobility and lifetime were also estimated. The electron mobility for an ultrapure BiI 3 detector was estimated to be approximately 433 cm 2/Vs while that for antimony doped BiI3 was estimated to be around 956 cm2/Vs and the mobility-lifetime product for electrons was estimated to be around 5.44 x 10-4 cm 2/V. Detector simulation was performed using the Monte Carlo simulation code MCNP5. A Matlab script which incorporates charge carrier trapping and statistical variation was written to generate a gamma-ray spectrum from the simulated energy deposition spectra. Measured and simulated spectra were compared to extract the charge carrier mobility-lifetime products, which for electrons and holes were estimated to be 5 x 10-3 cm2/V and 1.3 x

  6. Electrochemical reaction rates in a dye sentisised solar cell - the iodide/tri-iodide redox system

    DEFF Research Database (Denmark)

    Bay, Lasse; West, Keld; Winter-Jensen, Bjørn;

    2006-01-01

    The electrochemical reaction rate of the redox couple iodide / tri-iodide in acetonitrile is characterised by impedance spectroscopy. Different electrode materials relevant for the function of dye-sensitised solar cells (DSSC) are investigated. Preferably, the reaction with the iodide / tri......), and polyaniline (PANI) - all deposited onto fluorine doped tin oxide (FTO) glass. Both Pt and PEDOT are found to have sufficiently high catalytic activities for practical use as counter electrode in DSSC. The reaction resistance on FTO and anatase confirmed the beneficial effect of a compact anatase layer on top...

  7. Synthesis, Crystal Structure, and Luminescent Properties of New Zinc(II and Cadmium(II Metal-Organic Frameworks Based on Flexible Bis(imidazol-1-ylalkane Ligands

    Directory of Open Access Journals (Sweden)

    Marina Barsukova

    2016-10-01

    Full Text Available New metal-organic frameworks (MOFs based on zinc and cadmium ions, terephthalic acid, and flexible ligands 1,5-bis(imidazol-1-ylpentane or 1,6-bis(imidazol-1-ylhexane were prepared and characterized by X-ray diffraction, thermorgavimetric analysis and IR spectroscopy. The imidazolyl ligands were prepared by a new robust procedure involving the reaction between imidazole and 1,5-dibromopentane or 1,6-dibromohexane in a superbasic medium (KOH in DMSO. MOFs based on 1,5-bis(imidazol-1-ylpentane had diamond topology (dia and are triply interpenetrated. Ligands with longer spacer 1,6-bis(imidazol-1-ylhexane, terephthalate ions and zinc(II ions formed five-fold interpenetrated metal-organic framework also with dia topology, while cadmium(II ions with the same ligands formed eight-connected uninodal net with a very rare self-penetrated topological type ilc and a point symbol 424.5.63. The influence of the chemical composition of MOFs on their photoluminescent properties is investigated and discussed in detail.

  8. Synthesis, spectral, electrochemical, crystal structure studies of two novel di-μ-halo-bis[halo(2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline)cadmium(II)] dimer complexes and their thermolysis to nanometal oxides

    Science.gov (United States)

    Warad, Ismail; Abdoh, Muneer; Shivalingegowda, Naveen; Lokanath, Neartur Krishnappagowda; Salghi, Rachid; Al-Nuri, Mohammed; Jodeh, Shehdeh; Radi, Smaail; Hammouti, Belkheir

    2015-11-01

    Two new neutral dimer Cadmium(II) complexes, [Cd2(dmdphphen)2X4] and where X = Cl (complex 1), Br (complex 2), and dmdphphen = 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline, were synthesized and characterized by an elemental analysis, UV-Vis, IR, TG/DTA, CV and single crystal X-ray diffraction. Complex 1 crystallizes in the triclinic system with the space group P-1 with unit cell parameters a = 10.1124(8) Å, b = 10.8875(8) Å, c = 11.5730(9) Å, α = 108.323(3)°, β = 107.010(3)°, γ = 91.260(3)° V = 1147.51(15) Å3 and Z = 1. The Cd(II) ions are located in a slightly distorted square-pyramidal geometry. The complexes exhibit a quasi-reversible one electron response at -570 mV vs. Cp2Fe/Cp2Fe+, which has been assigned Cd(II)/Cd(III) couples. TG/DTA result shows that these complexes are very stable and decomposed through one step reaction. Calcination of Complex 1, revealed the formation of Cubic nanoparticle CdO.

  9. Investigation of sodium iodide hydration and dehydration in moist atmosphere

    International Nuclear Information System (INIS)

    Effect of different factors on NaI hydration and dehydration kinetics under nonequilibrium conditions is studied. NaIx2H2O solid or homogeneous solution is established to be formed at sodium iodide interaction with water vapour depending on air humidity. At low humidity water absorption is not observed. Effect of water vapour pressure, the NaI particle size, the air flux rate over a salt on the absorption rate is studied. The latter points to process rate limitation by diffusion in a gaseous phase. The NaI solution decomposition at light with iodine formation is marked. The character of NaIx2H2O dehydration depends on water vapour removing from the over-salt space. Total water removing before and after crystal hydrate thermal degradation when aqueous solution evaporation occurs, is possible. At 143 deg C the water vapour pressure over solution equals the atmospheric one

  10. 21 CFR 184.1265 - Cuprous iodide.

    Science.gov (United States)

    2010-04-01

    ... the following specific limitations: Category of food Maximum treatment level in food Functional use... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Cuprous iodide. 184.1265 Section 184.1265 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR...

  11. Electronic and optical properties of lead iodide

    DEFF Research Database (Denmark)

    Ahuja, R.; Arwin, H.; Ferreira da Silva, A.;

    2002-01-01

    The electronic properties and the optical absorption of lead iodide (PbI2) have been investigated experimentally by means of optical absorption and spectroscopic ellipsometry, and theoretically by a full-potential linear muffin-tin-orbital method. PbI2 has been recognized as a very promising...

  12. Cu-catalyzed trifluoromethylation of aryl iodides with trifluoromethylzinc reagent prepared in situ from trifluoromethyl iodide

    OpenAIRE

    Yuzo Nakamura; Motohiro Fujiu; Tatsuya Murase; Yoshimitsu Itoh; Hiroki Serizawa; Kohsuke Aikawa; Koichi Mikami

    2013-01-01

    The trifluoromethylation of aryl iodides catalyzed by copper(I) salt with trifluoromethylzinc reagent prepared in situ from trifluoromethyl iodide and Zn dust was accomplished. The catalytic reactions proceeded under mild reaction conditions, providing the corresponding aromatic trifluoromethylated products in moderate to high yields. The advantage of this method is that additives such as metal fluoride (MF), which are indispensable to activate silyl groups for transmetallation in the corresp...

  13. 乙醇-硫酸铵双水相萃取镉-碘化钾-罗丹明B离子缔合物%Extraction of cadmium-potassium iodide-rhodamine B ion association complex by alcohol-ammonium sulfate aqueous two-phase

    Institute of Scientific and Technical Information of China (English)

    曾云; 覃事栋; 姚康康; 王影; 肖苗

    2012-01-01

    In the presence of ammonium sulphate, the extraction behavior of Cd (Ⅱ) based on potassium iodide-Rhodamine B-alcohol system was studied and the optimal condition of phase separation was selected. Results showed that in the pH1 ~3 media, the extraction rate of [CdI4]2- by alcohol-ammonium sulfate aqueous two-phase system is only 35.5% , and the ion association complex, which is formed by adding rhodamine B, can be extracted completely by the aqueous two-phase system. In the system, Cd2+ can be dissociated completely from Zn2+, Fe3+, Co2+, Cu2+, and Ni2+.%研究了在( NH4) 2SO4存在下,碘化钾-罗丹明B-乙醇体系萃取Cd(Ⅱ)的行为及最佳分相条件.实验表明,在pH 1~3时,乙醇-( NH4 )2SO4双水相体系对[ CdI4]2-络阴离子的萃取率只有35.5%;加入罗丹明B后,该体系能完全萃取镉-碘化钾-罗丹明B形成的离子缔合物,而干扰离子Zn2+、Fe3+、Co2+、Cu2+、Ni2+不被萃取,实现Cd2+与上述离子的分离.

  14. Electrochemical reaction rates in a dye-sensitised solar cell - the iodide/tri-iodide redox system

    DEFF Research Database (Denmark)

    Bay, L.; West, K.; Winther-Jensen, B.;

    2006-01-01

    The electrochemical reaction rate of the redox couple iodide/tri-iodide in acetonitrile is characterised by impedance spectroscopy. Different electrode materials relevant for the function of dye-sensitised solar cells (DSSC) are investigated. Preferably, the reaction with the iodide/tri-iodide co......The electrochemical reaction rate of the redox couple iodide/tri-iodide in acetonitrile is characterised by impedance spectroscopy. Different electrode materials relevant for the function of dye-sensitised solar cells (DSSC) are investigated. Preferably, the reaction with the iodide......), and polyaniline (PANI)-all deposited onto fluorine-doped tin oxide (FTO) glass. Both Pt and PEDOT are found to have sufficiently high catalytic activities for practical use as counter electrodes in DSSC. The reaction resistance on FTO and anatase confirmed the beneficial effect of a compact anatase layer on top...

  15. Composition and properties of thallium mercury iodide

    Science.gov (United States)

    Kennedy, John H.; Schaupp, Christopher; Yang, Yuan; Zhang, Zhengming; Novinson, Thomas; Hoffard, Theresa

    1990-10-01

    Conflicting reports exist in the literature concerning the composition of thallium mercury iodide. Solid state synthesis with HgI 2 and TlI has been reported to give Tl 4HgI 6 while synthesis from solution has been reported to give Tl 2HgI 4. In this report we show that the "orange compound" precipitating from solution is actually a 1:1 mole ratio mixture of Tl 4HgI 6 and HgI 2. Pure Tl 4HgI 6, which is yellow, can be produced by heating the mixture at 100°C for several days to volatilize HgI 2 or more simply, by adding Tl(I) to a solution containing 2:1 KI:K 2HgI 4 to provide the additional iodide ions needed for Tl 4HgI 6. Tl 4HgI 6, unlike Ag 2HgI 4 and Cu 2HgI 4, has no sharp thermochromic changes and has no measurable ionic conductivity. This provides another example of the significant role the metal ion plans in determining structure and properties of metal mercury iodide compounds.

  16. Formation of cyanogen iodide by lactoperoxidase.

    Science.gov (United States)

    Schlorke, Denise; Flemmig, Jörg; Birkemeyer, Claudia; Arnhold, Jürgen

    2016-01-01

    The haem protein lactoperoxidase (LPO) is an important component of the anti-microbial immune defence in external secretions and is also applied as preservative in food, oral care and cosmetic products. Upon oxidation of SCN(-) and I(-) by the LPO-hydrogen peroxide system, oxidised species are formed with bacteriostatic and/or bactericidal activity. Here we describe the formation of the inter(pseudo)halogen cyanogen iodide (ICN) by LPO. This product is formed when both, thiocyanate and iodide, are present together in the reaction mixture. Using (13)C nuclear magnetic resonance spectroscopy and gas chromatography-mass spectrometry we could identify this inter(pseudo)halogen after applying iodide in slight excess over thiocyanate. The formation of ICN is based on the reaction of oxidised iodine species with thiocyanate. Further, we could demonstrate that ICN is also formed by the related haem enzyme myeloperoxidase and, in lower amounts, in the enzyme-free system. As I(-) is not competitive for SCN(-) under physiologically relevant conditions, the formation of ICN is not expected in secretions but may be relevant for LPO-containing products.

  17. Hydrothermal Synthesis, Crystal Structure and Luminescence Properties of a New 2D Cadmium Complex Based on the 4,4'-Bis(benzimidazol-1-ylmethy1)biphenyl and Glutaric Acid Ligands

    Institute of Scientific and Technical Information of China (English)

    TAO Zhao-Lin; QIN Ling; CUI Jie-Hu; ZHENG He-Gen

    2013-01-01

    A new polymeric complex {[Cd2(bbmb)2(gt)2]·(H2O)2}n (bbmb =4,4'-bis(benzimidazol-1-ylmethy1)biphenyl,H2gt =glutaric acid) has been obtained by hydrothermal method and structurally characterized by elemental analysis,IR,XRD,TGA and single-crystal X-ray diffraction.The complex belongs to the triclinic system,space group P(-1) with a =10.2417(15),b =13.752(2),c =22.201(3) (A),a =73.899(2),β =88.416(2),γ =78.305(2)°,V =2940.4(7) (A)3,Z =2,C66H56Cd2N8O8,Mr =1313.99,Dc =1.484 g/cm3,F(000) =1336 andμ =0.787 mm-1,and features a 2D network.In the solid state at room temperature,the cadmium(Ⅱ) complex exhibits strong fluorescence absorption at 435 nm (λmax).

  18. Chloride, bromide and iodide scintillators with europium doping

    Science.gov (United States)

    Zhuravleva, Mariya; Yang, Kan

    2014-08-26

    A halide scintillator material is disclosed where the halide may comprise chloride, bromide or iodide. The material is single-crystalline and has a composition of the general formula ABX.sub.3 where A is an alkali, B is an alkali earth and X is a halide which general composition was investigated. In particular, crystals of the formula ACa.sub.1-yEu.sub.yI.sub.3 where A=K, Rb and Cs were formed as well as crystals of the formula CsA.sub.1-yEu.sub.yX.sub.3 (where A=Ca, Sr, Ba, or a combination thereof and X=Cl, Br or I or a combination thereof) with divalent Europium doping where 0.ltoreq.y.ltoreq.1, and more particularly Eu doping has been studied at one to ten mol %. The disclosed scintillator materials are suitable for making scintillation detectors used in applications such as medical imaging and homeland security.

  19. Luminescence properties of Pb2+- and Mn2+-activated CdI2 crystals

    International Nuclear Information System (INIS)

    The luminescence properties of CdI2, CdI2:Pb2+, CdI2:Mn2+, and CdI2:(Pb2+,Mn2+) crystals have been studied at temperatures from 85 to 295 K under optical and X-ray excitation. Analysis of new and earlier spectroscopic data suggests that the 560-nm luminescence of CdI2:Pb2+ and CdI2:(Pb2+,Mn2+) crystals under excitation on the long-wavelength component of the A absorption band of Pb2+ centers is due to Pb2+-bound anion excitons. The 640- to 660-nm emission of these crystals is attributable to α centers. The manganese luminescence in the co-doped material originates from both intra-center Mn2+ excitations and a sensitized process due to energy transfer from the host and Pb2+-related centers. The mechanisms of recombination and energy transfer processes in cadmium iodide crystals co-doped with Pb2+ and Mn2+ are discussed

  20. Cadmium toxicity and treatment.

    Science.gov (United States)

    Bernhoft, Robin A

    2013-01-01

    Cadmium is a heavy metal of considerable toxicity with destructive impact on most organ systems. It is widely distributed in humans, the chief sources of contamination being cigarette smoke, welding, and contaminated food and beverages. Toxic impacts are discussed and appear to be proportional to body burden of cadmium. Detoxification of cadmium with EDTA and other chelators is possible and has been shown to be therapeutically beneficial in humans and animals when done using established protocols.

  1. Cadmium Toxicity and Treatment

    Directory of Open Access Journals (Sweden)

    Robin A. Bernhoft

    2013-01-01

    Full Text Available Cadmium is a heavy metal of considerable toxicity with destructive impact on most organ systems. It is widely distributed in humans, the chief sources of contamination being cigarette smoke, welding, and contaminated food and beverages. Toxic impacts are discussed and appear to be proportional to body burden of cadmium. Detoxification of cadmium with EDTA and other chelators is possible and has been shown to be therapeutically beneficial in humans and animals when done using established protocols.

  2. Cadmium Toxicity and Treatment

    OpenAIRE

    Bernhoft, Robin A.

    2013-01-01

    Cadmium is a heavy metal of considerable toxicity with destructive impact on most organ systems. It is widely distributed in humans, the chief sources of contamination being cigarette smoke, welding, and contaminated food and beverages. Toxic impacts are discussed and appear to be proportional to body burden of cadmium. Detoxification of cadmium with EDTA and other chelators is possible and has been shown to be therapeutically beneficial in humans and animals when done using established proto...

  3. Effect of nitrogen and oxygen on radiolysis of iodide solution

    Energy Technology Data Exchange (ETDEWEB)

    Karasawa, H.; Endo, M. [Hitachi Ltd., Power and Industrial System R+D Divisions, Ibaraki (Japan)

    1996-12-01

    The effect of nitrogen and oxygen on radiolysis of iodide solution was examined. Direct decomposition of nitrogen by {gamma}-radiation produced nitric acid to decrease a water pH. This resulted in the iodine formation in the radiolysis of iodide solution. Hydrogen peroxide was produced by the radiolysis of water containing oxygen. This worked a reducing agent to suppress the formation of iodine in the radiolysis of iodide solution. In the analytical model, fourteen iodine species were considered and reaction scheme consisted in 124 reactions. The analytical model could estimate the oxidation state of iodide ions. (author) 4 figs., 4 refs.

  4. Mercuric Iodide Anticoincidence Shield for Gamma-Ray Spectrometer Project

    Data.gov (United States)

    National Aeronautics and Space Administration — We utilize a new detector material, polycrystalline mercuric iodide, for background suppression by active anticoincidence shielding in gamma-ray spectrometers. Two...

  5. Mercuric Iodide Anticoincidence Shield for Gamma-Ray Spectrometer Project

    Data.gov (United States)

    National Aeronautics and Space Administration — We propose to utilize a new detector material, polycrystalline mercuric iodide, for background suppression by active anticoincidence shielding in gamma-ray...

  6. Syntheses, Crystal Structures and Photoluminescence Properties of Cadmium(Ⅱ) and Nickel(Ⅱ) Complexes with 2-(2-Benzimidazolyl)quinoline

    Institute of Scientific and Technical Information of China (English)

    CHEN Shu-Yang; GUO Ying-Chen; ZHANG Lian-Feng; FENG Yu-Quan; ZHENG Yuan-Yuan

    2013-01-01

    Two novel complexes,[Cd2(BMQU)2Cl4] (1) and [Ni(BMQU)2HPO4]·1.5H2O (2)(BMQU =2-(2-benzimidazolyl)quinoline),were synthesized by the hydrothermal method and characterized by elemental analysis,IR,and TG-DTG.The crystal structures were determined by single-crystal X-ray diffraction.Both 1 and 2 crystallize in the triclinic system,space group P(1).The data for 1:a =0.8342(7),b =0.9226(9),c =1.0646(8) nm,α =90.819(2),β =97.466(2),γ =98.280(2)°.The Cd(Ⅱ) is coordinated with three chlorine atoms and two nitrogen atoms of a BMQU molecule,generating a distorted square-pyramidal geometry.The dinuclear Cd(Ⅱ) complex is formed by two chlorine bridge bonds,and the one-dimensional chain structure is constructed with the hydrogen bond N-H…Cl and π-π stacking interaction.The data for 2:a =1.2251(1),b =1.2451(1),c =1.2868(1) nm,α =107.510(2),β =98.630(1),γ =109.921(2)°.The Ni(Ⅱ) is coordinated with four nitrogen atoms of two BMQU molecules and two oxygen atoms of a HPO42-,forming a distorted-octahedral geometry.The two-dimensional layer structure is formed by the hydrogen bonds and π-π stacking interaction between neighboring molecules.Complex 1 shows a strong blue fluorescence emission (λmax=456 nm) at solid state.

  7. Two novel interpenetrated zinc(Ⅱ) and cadmium(Ⅱ) coordination polymers based on 4-imidazole-benzoate: Syntheses, crystal structures and properties

    Institute of Scientific and Technical Information of China (English)

    BAI ZhengShuai; CHEN ShuiSheng; ZHANG ZhengHua; CHEN ManSheng; LIU GuangXiang; SUN WeiYin

    2009-01-01

    Two novel interpenetrated coordination polymers, [Zn(IBA)2]n (1) and {[Cd(IBA)2(H2O)]-4H2O}n (2),have been synthesized by using 4-imidazole-benzoic acid (HIBA) as ligand under hydrothermal con-ditions. Complex I crystallizes in a chiral space group and has a two-fold interpenetrated 2D network structure with (4,4) topology, while complex 2 is a 3D porous dia network with four nets interpene-trating each other. The SHG activity of 1 and the photoluminescent property of 2 have been investi-gated.

  8. Two novel interpenetrated zinc(Ⅱ) and cadmium(Ⅱ) coordination polymers based on 4-imidazole-benzoate:Syntheses,crystal structures and properties

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    Two novel interpenetrated coordination polymers,[Zn(IBA)2]n (1) and {[Cd(IBA)2(H2O)].4H2O}n (2),have been synthesized by using 4-imidazole-benzoic acid (HIBA) as ligand under hydrothermal con-ditions. Complex 1 crystallizes in a chiral space group and has a two-fold interpenetrated 2D network structure with (4,4) topology,while complex 2 is a 3D porous dia network with four nets interpene-trating each other. The SHG activity of 1 and the photoluminescent property of 2 have been investi-gated.

  9. Novel mercuric iodide polycrystalline nuclear particles counters

    Energy Technology Data Exchange (ETDEWEB)

    Schieber, M. [Hebrew Univ. of Jerusalem (Israel)]|[Sandia National Lab., Livermore, CA (United States); Zuck, A.; Braiman, M.; Nissenbaum, J. [Hebrew Univ. of Jerusalem (Israel)] [and others

    1996-12-31

    Polycrystalline mercuric iodide nuclear radiation detectors having areas between 0.01 to 100 cm{sup 2} and thicknesses 30 to 600 microns, have been fabricated with single, linear strip and square pixel contact. The large area detectors 10 to 600 cm{sup 2} were produced by industrial ceramic equipment while the smaller ones, about 1 cm{sup 2} area, were produced in the laboratory. The large detectors still had large leakage currents and the production process is being revised. The smaller detectors were tested and their response to lower and higher gamma energy, beta and even 100 GeV muons at CERN will be reported.

  10. Transfer of the human sodium/iodide symporter gene enhances iodide uptake in melanoma cells

    International Nuclear Information System (INIS)

    Objective: To obtain human sodium/iodide symporter (hNIS) cDNA and to study its biological property and potential use as a therapeutic radioiodide for melanoma. Methods: hNIS gene cDNA was amplified with total RNA from human thyroid tissue by RT-PCR. The hNIS cDNA was inserted into cloning vector pUCm-T and subcloned into eukaryotic expression vector pcDNA3. The recombinant plasmid pcDNA3-hNIS was introduced into B16 cells using the electroporation technique. The uptake and efflux of iodide was examined in vitro. Results: The cloned hNIS cDNA sequence was identical to the published sequence. Two novel cell lines named B16-A containing hNIS and B16-B containing pcDNA3 only were established. The resultant cell line B16-A accumulated 17 and 19 times more radioiodide in vitro than B16 and B16-B did, respectively. However the efflux of iodide from B16-A was also rapid ( T1/2=10 min). Conclusions: Our preliminary data indicate that the transduction of the hNIS gene per se is sufficient to induce iodide transport in melanoma cells in vitro, but its T1/2 is short. With regard to therapeutic application, however, further investigation is necessary so as to develop a method of maintaining more radioiodide in the cells for long enough to produce greater therapeutic effects

  11. Synthesis of cadmium complexes of 4'-chloro-terpyridine: From discrete dimer to 1D chain polymer, crystal structure and antibacterial activity

    Indian Academy of Sciences (India)

    Lotfali Saghatforoush; Laura Valencia Matarranz; Firoozeh Chalabian; Shahriare Ghammamy; Fatemeh Katouzian

    2012-05-01

    Two new Cd(II) complexes with the ligand 4'-chloro-2,2':6',2"-terpyridine (Cltpy), [Cd(Cltpy)(N3)(CH3COO)], 1, and [Cd(Cltpy)(NCS)(CH3COO)], 2, have been synthesized and characterized by CHN elemental analyses, 1HNMR-, 13C NMR-, IR spectroscopy and structurally analysed by X-ray singlecrystal diffraction. The single crystal X-ray analyses show that the coordination number in these complexes is seven with three terpyridine (Cltpy) N-donor atoms, two acetate oxygens and two anionic bridged ligands. The crystal structure of 2 comprises a one-dimensional polymeric network bridged by NCS− anions. The antibacterial activities of Cltpy and its Cd(II) complexes are tested against different bacteria. Both complexes have shown good activity against all the tested bacteria. Against Klebsiella pneumonia and Staphylococcus aureus, antibacterial activity of complexes is higher than Cltpy ligand. The higher activity of complexes may be explained on the basis of chelation theory.

  12. Hydrothermal Synthesis and Crystal Structure of a Cadmium(Ⅱ) Polymer with One-dimensional Chain Structure: [Cd(bpy)(BDC)]n·nbpy

    Institute of Scientific and Technical Information of China (English)

    LI Xiu-Mei; NIU Yan-Ling; WANG Qing-Wei; CUI Yun-Cheng; LIU Bo

    2007-01-01

    A metal-organic coordination polymer [Cd(bpy)(BDC)]n·nbpy (bpy = 2,2'-bipyri- dine, H2BDC = terephthalic acid) has been hydrothermally synthesized and structurally characteri- zed by elemental analysis, IR spectrum, TG and single-crystal X-ray diffraction. The complex crystallizes in monoclinic, space group C2/c with a = 15.723(5), b = 21.695(5), c = 7.576(5)(A), β = 116.171(7)o, V = 2319.3(18)(A)3, C28H20CdN4O4, Mr = 588.88, Dc = 1.686 g/cm3, μ(MoKα) = 0.987 mm(1, F(000) = 1184, Z = 4, the final R = 0.0464 and wR = 0.0831 for 1882 observed reflections (Ⅰ > 2σI)). It exhibits a three-dimensional network with channels constructed from one-dimensional coordination chains via C-H…O hydrogen bonds and significant aromatic π-π stacking interactions.

  13. Hydrothermal Synthesis and Crystal Structure of a Cadmium(Ⅱ) Polymer with One-dimensional Chain Structure: [Cd(MDPPz)(BDC)(H2O)]n

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    A metal-organic coordination compound formulated as [Cd(MDPPz)(BDC)(H2O)]n 1 (MDPPz = 11-methyldipyrido[3,2-a:2',3'-c]phenazine, BDC = 1,4-benzenedicarboxylate) has been hydrothermally synthesized and structurally characterized by elemental analysis, IR spectrum, fluorescence spectrum and single-crystal X-ray diffraction. The title compound crystallizes in the monoclinic system, space group C2/c, with a = 30.673(8), b = 9.623(3), c = 20.784(6) (A), β = 98.646(3)o, V = 6065(3) (A)3, C27H17CdN4O5, Mr = 589.85, Dc = 1.292 g/cm3, μ(MoKα) = 0.757 mm(1, F(000) = 2360, Z = 8, the final R = 0.0381 and wR = 0.0855 for 4191 observed reflections (I>2σ(I)). 1 exhibits blue fluorescence property at room temperature.

  14. Synthesis aspects, structural, spectroscopic, antimicrobial and room temperature ferromagnetism of zinc iodide complex with Schiff based ligand

    Science.gov (United States)

    Shakila, K.; Kalainathan, S.

    2015-01-01

    In this paper, we report the successful growth of complex compound of zinc iodide with thiocarbamide by slow evaporation method. The single crystal XRD study reveals that the crystal belongs to monoclinic system with centrosymmetric space group and powder XRD analysis shows that the perfect crystalline nature of the crystal. The presence of functional group and element were confirmed from FT-IR and EDAX analysis. Optical absorbance of the grown crystal was studied by UV-Vis spectrophotometer. The optical constants were calculated from the optical absorbance data such as refractive index (n), extinction coefficient (K) and reflectance (R). The optical band gap (Eg) of thiocarbamide zinc iodide crystal is 4.22 eV. The magnetic properties of grown crystal have been determined by Vibrating Sample Magnetometry (VSM). Room temperature magnetization revealed a ferromagnetic behaviour for the grown crystal. The antibacterial and antifungal activities of the title compound were performed by well diffusion method and MIC method against the standard bacteria like Staphylococcus aureus, Escherichia coli, Klebsiella pneumonia and against fungus like Aspergillus niger, Rhizopus sps and Penicillium sps. Thermal behaviour of the crystal has been investigated using thermogravimetric analysis (TGA) and differential thermal analysis (DTA).

  15. Phase 2 Methyl Iodide Deep-Bed Adsorption Tests

    Energy Technology Data Exchange (ETDEWEB)

    Soelberg, Nick [Idaho National Lab. (INL), Idaho Falls, ID (United States); Watson, Tony [Idaho National Lab. (INL), Idaho Falls, ID (United States)

    2014-09-01

    Nuclear fission produces fission products (FPs) and activation products, including iodine-129, which could evolve into used fuel reprocessing facility off-gas systems, and could require off-gas control to limit air emissions to levels within acceptable emission limits. Research, demonstrations, and some reprocessing plant experience have indicated that diatomic iodine can be captured with efficiencies high enough to meet regulatory requirements. Research on the capture of organic iodides has also been performed, but to a lesser extent. Several questions remain open regarding the capture of iodine bound in organic compounds. Deep-bed methyl iodide adsorption testing has progressed according to a multi-laboratory methyl iodide adsorption test plan. This report summarizes the second phase of methyl iodide adsorption work performed according to this test plan using the deep-bed iodine adsorption test system at the Idaho National Laboratory (INL), performed during the second half of Fiscal Year (FY) 2014. Test results continue to show that methyl iodide adsorption using AgZ can achieve total iodine decontamination factors (DFs, ratios of uncontrolled and controlled total iodine levels) above 1,000, until breakthrough occurred. However, mass transfer zone depths are deeper for methyl iodide adsorption compared to diatomic iodine (I2) adsorption. Methyl iodide DFs for the Ag Aerogel test adsorption efficiencies were less than 1,000, and the methyl iodide mass transfer zone depth exceeded 8 inches. Additional deep-bed testing and analyses are recommended to (a) expand the data base for methyl iodide adsorption under various conditions specified in the methyl iodide test plan, and (b) provide more data for evaluating organic iodide reactions and reaction byproducts for different potential adsorption conditions.

  16. Dissolution of gaseous methyl iodide into aqueous sodium hydroxide solutions

    International Nuclear Information System (INIS)

    Absorption process of gaseous methyl iodide by water or sodium hydroxide solutions was investigated using a semi-flow type experimental apparatus by measuring the concentration of all measurable chemical species in both the gas and the liquid phase. The experimental temperature ranged from 288 to 311 K and the gaseous methyl iodide and aqueous sodium hydroxide concentrations were approximately 0.6 x 10-3 to 7 x 10-3 and 0 to 0.2 mol/dm3, respectively. It is estimated that the dissolution of methyl iodide into the sodium hydroxide solution proceeds according to the following steps. Step (1) Methyl iodide in air dissolves physically into the aqueous phase. Physical dissolution process obeys Henry's law. Step (2) Methyl iodide dissolved into the aqueous phase is decomposed by a base catalytic hydrolysis and produces methyl alcohol and iodide ion. The equilibrium constants of physical dissolution were obtained from the steady concentration in both the gas and the liquid phases in the semi-flow type experiment because the hydrolysis reaction rate of methyl iodide is very slow in comparison with the physical dissolution in this experimental conditions. The obtained value of the standard heat of solution of methyl iodide into water was 7.2 kcal/mol. Salting-out effect was observed when the concentration of sodium hydroxide in the absorbent was over 0.01 mol/dm3. (auth.)

  17. Zinc and cadmium monosalicylates

    Energy Technology Data Exchange (ETDEWEB)

    Kharitonov, Yu.Ya.; Tujebakhova, Z.K. (Moskovskij Khimiko-Tekhnologicheskij Inst. (USSR))

    1984-06-01

    Zinc and cadmium monosalicylates of the composition MSal, where M-Zn or Cd, Sal - twice deprotonated residue of salicylic acid O-HOC/sub 6/H/sub 4/COOH (H/sub 2/Sal), are singled out and characterized. When studying thermograms, thermogravigrams, IR absorption spectra, roentgenograms of cadmium salicylate compounds (Cd(OC/sub 6/H/sub 4/COO) and products of their thermal transformations, the processes of thermal decomposition of the compounds have been characterized. The process of cadmium monosalicylate decomposition takes place in one stage. Complete loss of salicylate acido group occurs in the range of 320-460 deg. At this decomposition stage cadmium oxide is formed. A supposition is made that cadmium complex has tetrahedral configuration, at that, each salicylate group plays the role of tetradentate-bridge ligand. The compound evidently has a polymer structure.

  18. Digermylene Oxide Stabilized Group 11 Metal Iodide Complexes.

    Science.gov (United States)

    Yadav, Dhirendra; Siwatch, Rahul Kumar; Sinhababu, Soumen; Karwasara, Surendar; Singh, Dharmendra; Rajaraman, Gopalan; Nagendran, Selvarajan

    2015-12-01

    Use of a substituted digermylene oxide as a ligand has been demonstrated through the isolation of a series of group 11 metal(I) iodide complexes. Accordingly, the reactions of digermylene oxide [{(i-Bu)2ATIGe}2O] (ATI = aminotroponiminate) (1) with CuI under different conditions afforded [({(i-Bu)2ATIGe}2O)2(Cu4I4)] (2) with a Cu4I4 octahedral core, [({(i-Bu)2ATIGe}2O)2(Cu3I3)] (3) with a Cu3I3 core, and [{(i-Bu)2ATIGe}2O(Cu2I2)(C5H5N)2] (4) with a butterfly-type Cu2I2 core. The reactions of compound 1 with AgI and AuI produced [({(i-Bu)2ATIGe}2O)2(Ag4I4)] (5) with a Ag4I4 octahedral core and [{(i-Bu)2ATIGe}2O(Au2I2)] (6) with a Au2I2 core, respectively. The presence of metallophilic interactions in these compounds is shown through the single-crystal X-ray diffraction and atom-in-molecule (AIM) studies. Preliminary photophysical studies on compound 6 are also carried out. PMID:26558406

  19. Coordination compounds of manganese(2) and cadmium(2) with α-ketoacid thiosemicarbazones

    International Nuclear Information System (INIS)

    Manganese (2) and cadmium (2) coordination compounds with gluoxalic, pyroacemic and benzoyl formic acid thiosemicarbazones are synthesized. ESR spectra of polycrystalline samples of manganese compounds and cadmium compounds activated with manganese at T=113 295 deg K allow to suppose that Mn2+ takes the position of Cd2+ ion which is in a weakly distorted octahedron crystal field

  20. A review of recent measurements of optical and thermal properties of. alpha. -mercuric iodide

    Energy Technology Data Exchange (ETDEWEB)

    Burger, A.; Morgan, S.H.; Silberman, E. (Fisk Univ., Nashville, TN (United States). Dept. of Physics); Nason, D.; Cheng, A.Y. (EG and G Energy Measurements, Inc., Goleta, CA (United States). Santa Barbara Operations)

    1991-01-01

    The knowledge of the physical properties of a crystal and their relation to the nature and content of defects are essential for both applications and fundamental reasons. Alpha-mercuric iodide ({alpha}-HgI{sub 2}) is a material which was found important applications as room temperature X-ray and gamma ray detectors. Some recent thermal and optical measurements of this material, using the samples of improved crystallinity which are now available, are reviewed below. Heretofore, these properties have received less attention than the mechanical and electrical properties, particularly at elevated temperatures. In the technology of {alpha}-HgI{sub 2} where there is a continuing motivation to obtain larger single crystals without compromising the material quality, a better knowledge of the thermal and optical properties may lead to improvements in the processes of material purification, crystal growth and device fabrication.

  1. Crystal structure of cis-bis­{4-phenyl-1-[(3R)-1,7,7-tri­methyl-2-oxobi­cyclo­[2.2.1]heptan-3-ylidene]thio­semicarbazidato-κ3 O,N 1,S}cadmium(II) with an unknown solvent mol­ecule

    OpenAIRE

    Nogueira, Vanessa Senna; Bresolin, Leandro; Näther, Christian; Jess, Inke; de Oliveira, Adriano Bof

    2015-01-01

    The reaction between the racemic mixture of the camphor-4-phenyl­thio­semicarbazone derivative and cadmium acetate dihydrate yielded the title compound, [Cd(C17H20N3OS)2]. The CdII ion is six-coordinated in a distorted octa­hedral environment by two deprotonated thio­semicarbazone ligands acting as an O,N,S-donor in a tridentate chelating mode, forming five-membered chelate rings. In the crystal, the mol­ecules are connected via pairs of N—H⋯S and C—H⋯S inter­actions, building centrosymmetric...

  2. Crystal structure of cis-bis{4-phenyl-1-[(3R)-1,7,7-trimethyl-2-oxobicyclo[2.2.1]heptan-3-ylidene]thiosemicarbazidato-κ3O,N1,S}cadmium(II) with an unknown solvent molecule

    OpenAIRE

    Vanessa Senna Nogueira; Leandro Bresolin; Christian Näther; Inke Jess; Adriano Bof de Oliveira

    2015-01-01

    The reaction between the racemic mixture of the camphor-4-phenylthiosemicarbazone derivative and cadmium acetate dihydrate yielded the title compound, [Cd(C17H20N3OS)2]. The CdII ion is six-coordinated in a distorted octahedral environment by two deprotonated thiosemicarbazone ligands acting as an O,N,S-donor in a tridentate chelating mode, forming five-membered chelate rings. In the crystal, the molecules are connected via pairs of N—H...S and C—H...S interactions, building centrosymmetric d...

  3. New measurement of the Fano factor of mercuric iodide. [astronomical x-ray detector charge collection efficiency

    Science.gov (United States)

    Ricker, G. R.; Vallerga, J. V.; Dabrowski, A. J.; Iwanczyk, J. S.; Entine, G.

    1982-01-01

    It is pointed out that mercuric iodide (HgI2) shows great promise as a high-resolution X-ray detector for use in X-ray astronomy. Development of mercuric iodide for astronomical work has required investigation of the temperature dependence of the HgI2 crystal parameters such as leakage current, resolution, and mobility of the charge carriers. The first studies in connection with these investigations have led to a new value of the Fano factor of 0.19 + or - 0.03. The best value previously reported was 0.27 measured at room temperature. The new upper limit of 0.19 for the HgI2 Fano factor was determined by cooling the HgI2 crystal and preamp to -20 C. It is concluded that room-temperature energy resolution of HgI2 is not limited by charge generation statistics but rather by collection efficiency.

  4. The use of mercuric iodide in instruments for safeguards and non-proliferation applications

    International Nuclear Information System (INIS)

    Mercuric Iodide is a material exceptionally suited for solid state detectors operating at room temperature. The high density and the high atomic numbers of the constituent elements provide a large absorption factor and a high full-energy-peak efficiency at gamma ray energies. The large electronic bandgap results in a very high resistivity and therefore a low leakage current at temperatures within and outside the personal comfort range. Constellation Technology has developed the technology to grow large, high quality crystals from mercuric iodide. Spectrometry grade detectors with dimensions of 25 mm x 25 mm x 3 mm and with an energy resolution of approximately 3% FWHM at 662 keV can be fabricated from these mercuric iodide crystals. The resolution of this detector approximately 1.8% FWHM and the peak-to-valley ratio is larger than twelve. Standard semi-Gaussian processing and no pulse-shape discrimination was used. These detectors can be conveniently incorporated into hand-held instruments to detect weak sources or heavily shielded sources. Previous measurements have shown that the Minimum Detectable Activity (MDA) of a 3 mm thick mercuric iodide detector with dimensions as given above is about 10% less than the MDA of a 50 mm x 50 mm sodium iodide detector, due to the superior energy resolution. Software methods are being developed to improve the identification of weak sources against a large background. Results of these measurements will be presented. Smaller detectors can be used in safeguards applications where the intensity of the radiation is relatively high. The spectral resolution of the detectors is high enough to clearly identify the significant energy lines in the spectra of stored uranium and plutonium. The shape of the spectral peaks is constant over a large range of energies so that existing software systems can be used to analyze the spectra. The small size, ruggedness, temperature stability and high efficiency of these detectors makes them good

  5. Ferroelastic Fingerprints in Methylammonium Lead Iodide Perovskite

    KAUST Repository

    Hermes, Ilka M.

    2016-02-12

    Methylammonium lead iodide (MAPbI3) perovskite materials show an outstanding performance in photovoltaic devices. However, certain material properties, especially the possible ferroic behavior, remain unclear. We observed distinct nanoscale periodic domains in the piezoresponse of MAPbI3(Cl) grains. The structure and the orientation of these striped domains indicate ferroelasticity as their origin. By correlating vertical and lateral piezoresponse force microscopy experiments performed at different sample orientations with x-ray diffraction, the preferred domain orientation was suggested to be the a1-a2-phase. The observation of these ferroelastic fingerprints appears to strongly depend on the film texture and thus the preparation route. The formation of the ferroelastic twin domains could be induced by internal strain during the cubic-tetragonal phase transition.

  6. Mercuric iodide research and development in support of DOE Historically Black Colleges and University Program. Semiannual technical progress report

    Energy Technology Data Exchange (ETDEWEB)

    George, M.A.; Zheng, Y.; Salary, L.; Chen, K.T.; Burger, A.

    1994-10-31

    This report describes the progress achieved during the first six months of the program. The different subjects studied were: zone refining experiments of mercuric iodide to establish optimum refining parameters and produce purified material; development of surface reflection spectroscopy as a method to measure crystal surface temperatures, with emphasis on investigation the potential of using optical multichannel analysis; optical methods for measuring iodine vapor during physical vapor transport of HgI{sub 2}; and atomic force microscopy studies.

  7. Conserved charged amino acid residues in the extracellular region of sodium/iodide symporter are critical for iodide transport activity

    Directory of Open Access Journals (Sweden)

    Liang Ji-An

    2010-11-01

    Full Text Available Abstract Background Sodium/iodide symporter (NIS mediates the active transport and accumulation of iodide from the blood into the thyroid gland. His-226 located in the extracellular region of NIS has been demonstrated to be critical for iodide transport in our previous study. The conserved charged amino acid residues in the extracellular region of NIS were therefore characterized in this study. Methods Fourteen charged residues (Arg-9, Glu-79, Arg-82, Lys-86, Asp-163, His-226, Arg-228, Asp-233, Asp-237, Arg-239, Arg-241, Asp-311, Asp-322, and Asp-331 were replaced by alanine. Iodide uptake abilities of mutants were evaluated by steady-state and kinetic analysis. The three-dimensional comparative protein structure of NIS was further modeled using sodium/glucose transporter as the reference protein. Results All the NIS mutants were expressed normally in the cells and targeted correctly to the plasma membrane. However, these mutants, except R9A, displayed severe defects on the iodide uptake. Further kinetic analysis revealed that mutations at conserved positively charged amino acid residues in the extracellular region of NIS led to decrease NIS-mediated iodide uptake activity by reducing the maximal rate of iodide transport, while mutations at conserved negatively charged residues led to decrease iodide transport by increasing dissociation between NIS mutants and iodide. Conclusions This is the first report characterizing thoroughly the functional significance of conserved charged amino acid residues in the extracellular region of NIS. Our data suggested that conserved charged amino acid residues, except Arg-9, in the extracellular region of NIS were critical for iodide transport.

  8. Cadmium status in Egypt

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    It is inferred from these studies that releases of Cd are still increasing and it is recommended that measures must be taken to reduce emissions of cadmium. Any cadmium discharged into the Egyptian environment may move from one compartment to another at varying rates,resulting in an accumulation in compartments such as soils and biota. Such accumulation can be expected to increase with continued emissions,and attention should be given to all sources of cadmium, natural as well as anthropogenic especially in the industrial cities in Egypt. Cadmium present in sewage, as well as industrial effluent (also, other liquid and solid wastes) and sewage sludge will increase levels in soils and is xpected to contribute to dietary levels and body burdens. The current information indicates that such effects may have to be evaluated over long periods of time, possibly as long as 50 - 100 years.

  9. Transport and deposition of halide in alkali metal-stainless steel systems, (IV). Measurement of sodium iodide solubility in sodium with major constituents of stainless steel and oxide in sodium

    International Nuclear Information System (INIS)

    Solubility of sodium iodide in sodium is measured separately (a) with concentrations of major constituents leached from stainless steel in sodium and (b) with controlled concentration of oxide in sodium by the use of stainless steel capsule. The capsules loaded with 20 g sodium and 0.1-0.3 g powder of additives are heated at their upper part in a furnace and cooled at their bottom on brass plates. (a) After a given period of run for sodium iodide equilibration, the distribution of the iodide and constituents is fixed in solidified sodium by quenching the capsules. Sodium samples taken from the sectioned capsule tube are submitted to sodium dissolution by steam for determining the iodide and to vacuum distillation for determining the constituents. The iodide solubility appears to be in a reverse correlation with concentrations of iron and nickel and to be insensitive to change in those of chromium, manganese and silicon. (b) After a given period of run for sodium oxide equilibration, the sodium is solidified by quenching the capsule. Deposits on the capsule bottom is removed by sectioning the capsule tube and crystals of sodium iodide are introduced to the sectioned capsule on which an end plug is seal-welded. The capsule is again set under the large temperature gradient for a period of run for iodide equilibration. After fixing the iodide distribution in solidified sodium by the quenching, sodium samples are taken from the sectioned capsule tube and submitted to the sodium dissolution by steam for determining iodide in sodium. The iodide solubility data obtained from the present measurement are observed to be scarcely affected by the oxide concentration. (author)

  10. Equations of state for crystalline zirconium iodide: The role of dispersion

    Science.gov (United States)

    Rossi, Matthew L.; Taylor, Christopher D.

    2013-02-01

    We present the first-principle equations of state of several zirconium iodides, ZrI2, ZrI3, and ZrI4, computed using density functional theory methods that apply various methods for introducing the dispersion correction. Iodides formed due to reaction of molecular or atomic iodine with zirconium and zircaloys are of particular interest due to their application to the cladding material used in the fabrication of nuclear fuel rods. Stress corrosion cracking (SCC), associated with fission product chemistry with the clad material, is a major concern in the life cycle of nuclear fuels, as many of the observed rod failures have occurred due to pellet-cladding chemical interactions (PCCI) [A. Atrens, G. Dannhäuser, G. Bäro, Stress-corrosion-cracking of zircaloy-4 cladding tubes, Journal of Nuclear Materials 126 (1984) 91-102; P. Rudling, R. Adamson, B. Cox, F. Garzarolli, A. Strasser, High burn-up fuel issues, Nuclear Engineering and Technology 40 (2008) 1-8]. A proper understanding of the physical properties of the corrosion products is, therefore, required for the development of a comprehensive SCC model. In this particular work, we emphasize that, while existing modeling techniques include methods to compute crystal structures and associated properties, it is important to capture intermolecular forces not traditionally included, such as van der Waals (dispersion) correction. Furthermore, crystal structures with stoichiometries favoring a high I:Zr ratio are found to be particularly sensitive, such that traditional density functional theory approaches that do not incorporate dispersion incorrectly predict significantly larger volumes of the lattice. This latter point is related to the diffuse nature of the iodide electron cloud.

  11. Removal of Cadmium Ions from Aqueous Solution by Silicate-incorporated Hydroxyapatite

    Institute of Scientific and Technical Information of China (English)

    SHI Hebin; ZHONG Hong; LIU Yu; DENG Jinyang

    2007-01-01

    This article reports a preliminary research on silicate-incorporated hydroxyapatite as a new environmental mineral used to remove cadmium ions from aqueous solutions. The silicate-incorporated hydroxyapatite was prepared by coprecipitation and calcining, and silicate was incorporated into the crystal lattice of hydroxyapatite by partial substitution of phosphate. The amount of cadmium ions removed by silicate-incorporated hydroxyapatite was significantly elevated, which was 76% higher than that of pure hydroxyapatite. But the sorption behavior of cadmium ions on silicate-incorporated hydroxyapatite was similar to that of pure hydroxyapatite. Morphological study revealed that silicate incorporation confined the crystal growth and increased the specific surface area of hydroxyapatite,which were in favor of enhancing the cadmium ion sorpfion capacity of the samples. Incorporation of silicate into hydroxyapatite seems to be an effective approach to improve the environmental property of hydroxyapatite on removal of aqueous cadmium ions.

  12. The Effect on Sodium/Iodide Symporter and Pendrin in Thyroid Colloid Retention Developed by Excess Iodide Intake.

    Science.gov (United States)

    Chen, Xiao-Yi; Lin, Chu-Hui; Yang, Li-Hua; Li, Wang-Gen; Zhang, Jin-Wei; Zheng, Wen-Wei; Wang, Xiang; Qian, Jiang; Huang, Jia-Luan; Lei, Yi-Xiong

    2016-07-01

    It is well known that excess iodide can lead to thyroid colloid retention, a classic characteristic of iodide-induced goiter. However, the mechanism has not been fully unrevealed. Iodide plays an important role in thyroid function at multiple steps of thyroid colloid synthesis and transport among which sodium/iodide symporter (NIS) and pendrin are essential. In our study, we fed female BALB/c mice with different concentrations of high-iodine water including group A (control group, 0 μg/L), group B (1500 μg/L), group C (3000 μg/L), group D (6000 μg/L), and group E (12,000 μg/L). After 7 months of feeding, we found that excess iodide could lead to different degrees of thyroid colloid retention. Besides, NIS and pendrin expression were downregulated in the highest dose group. The thyroid iodide intake function detected by urine iodine assay and thyroidal (125)I experiments showed that the urine level of iodine increased, while the iodine intake rate decreased when the concentration of iodide used in feeding water increased (all p control group). In addition, transmission electron microscopy (TEM) indicated a reduction in the number of intracellular mitochondria of thyroid cells. Based on these findings, we concluded that the occurrence of thyroid colloid retention exacerbated by excess iodide was associated with the suppression of NIS and pendrin expression, providing an additional insight of the potential mechanism of action of excess iodide on thyroid gland. PMID:26660892

  13. Expression of the human sodium/iodide symporter (hNIS) in xenotransplanted human thyroid carcinoma

    NARCIS (Netherlands)

    Smit, J.W.A.; Schröder - van der Elst, J.P.; Karperien, M.; Que, I.; Romijn, J.A.; Heide, van der D.

    2001-01-01

    The uptake of iodide in thyroid epithelial cells is mediated by the sodium/iodide symporter (NIS). The uptake of iodide is of vital importance for thyroid physiology and is a prerequisite for radioiodine therapy in thyroid cancer. Loss of iodide uptake due to diminished expression of the human NIS (

  14. Improved Stability of Mercuric Iodide Detectors for Anticoincidence Shields Project

    Data.gov (United States)

    National Aeronautics and Space Administration — We propose to utilize guard ring electrode structures and a new film growth technique to create improved polycrystalline mercuric iodide detectors for background...

  15. Prevention of organic iodide formation in BWR`s

    Energy Technology Data Exchange (ETDEWEB)

    Karjunen, T. [Finnish Centre for Radiation and Nuclear Safety, Helsinki (Finland); Laitinen, T.; Piippo, J.; Sirkiae, P. [VTT Manufacturing Technology (Finland)

    1996-12-01

    During an accident, many different forms of iodine may emerge. Organic iodides, such as methyl iodide and ethyl iodide, are relatively volatile, and thus their appearance leads to increased concentration of gaseous iodine. Since organic iodides are also relatively immune to most accident mitigation measures, such as sprays and filters, they can affect the accident source term significantly even when only a small portion of iodine is in organic form. Formation of organic iodides may not be limited by the amount of organic substances available. Excessive amounts of methane can be produced, for example, during oxidation of boron carbide, which is used in BWR`s as a neutron absorber material. Another important source is cable insulation. In a BWR, a large quantity of cables is placed below the pressure vessel. Thus a large quantity of pyrolyse gases will be produced, should the vessel fail. Organic iodides can be formed as a result of many different reactions, but at least in certain conditions the main reaction takes place between an organic radical produced by radiolysis and elemental iodine. A necessary requirement for prevention of organic iodide production is therefore that the pH in the containment water pools is kept high enough to eliminate formation of elemental iodine. In a typical BWR the suppression pool water is usually unbuffered. As a result, the pH may be dominated by chemicals introduced during an accident. If no system for adding basic chemicals is operable, the main factor affecting pool water pH may be hydrochloric acid released during cable degradation. Should this occur, the conditions could be very favorable for production of elemental iodine and, consequently, formation of organic iodides. Although high pH is necessary for iodine retention, it could have also adverse effects. High pH may, for example, accelerate corrosion of containment materials and alter the characteristics of the solid corrosion products. (author) 6 figs., 1 tab., 13 refs.

  16. A review of polytypism in lead iodide

    Energy Technology Data Exchange (ETDEWEB)

    Beckmann, P.A. [Department of Physics, Bryn Mawr College, Bryn Mawr, Pennsylvania (United States)

    2010-05-15

    Lead Iodide (PbI{sub 2}) is an important inorganic solid for both basic scientific research and possible technological applications and in this brief review we discuss the structure of PbI{sub 2}. Although the basic structure is a simple I-Pb-I layered structure with a[PbI{sub 6}]{sup 4-} near-octahedron being the basic building block, there are many ways of stacking the layers which results in many polytypes. We present 20 of the 23 entries for the structure of PbI{sub 2} from the Inorganic Structural Database and order them by polytype. This represents more than 80 years of crystallographic research in the structure of this compound. We present a simple way to view the 2H, 4H, 6H, and 6R polytypes and extend the procedure to higher-order polytypes. We note a relationship, not generally appreciated, between the distortion of the near [PbI{sub 6}]{sup 4-} octahedrons and the polytype. We suggest that the significance of vacancies has only recently been appreciated. We suggest that small discrepancies in structure determination are probably due to different distributions of vacancies and that there are, in practice, very many structures for macroscopic or even mesoscopic samples of a given polytype when vacancies are considered. (copyright 2010 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  17. Plausible Mechanisms of Cadmium Carcinogenesis

    Science.gov (United States)

    Cadmium is a transition metal and an ubiquitous environmental and industrial pollutant. Laboratory animal studies and epidemiological studies have shown that exposure to cadmium is associated with various organ toxicities and carcinogenic effects. Several national and internation...

  18. Investigations of portable cadmium telluride (CdTe(Cl)) detectors for clinical studies with radioactive indicators

    International Nuclear Information System (INIS)

    The combination of small, portable γ-radiation-sensitive Cadmium Telluride (CdTE(Cl)) crystal detectors and portable solid state data storage memories makes it feasible to extend the measuring period in a number of clinical investigations based on the use of various radioisotopes and external detection. Blood sampling can be avoided in some cases. Continuous ambulatory monitoring of relevant physiological parameters is practicable, e.g. kidney function (GFR), left ventricular ejection fraction, subcutaneous blood flow, muscle blood flow and insulin absorption in diabetic patients. In the present methodological study the applicability of the 133-Xe washout technique to subcutaneous (s.c.) adipose tissue blood flow (SBF) has been investigated and adapted to the use of CdTe(Cl) detectors attached to the skin surface for the measurement of local 133-Xe-disappearance rate constants (k). Physical characterization of CdTe(Cl) detectors as γ-sensitive devices has been performed, and adequate counting sensitivities were found without detector energy-resolution properties. The CdTe(Cl) detectors are therefore suitable for single indicator studies. The measuring geometry of CdTe(Cl) detectors was studied and compared with that of stationary Sodium Iodide (NaI(Tl)) detectors in both phantom and in vivo investigations. The spatial properties of CdTe(Cl) detectors could to some extent be adjusted by pulse height discrimination and lead collimation. When long-term measurements were complicated by for instance physical activity of the patients, the small CdTe(Cl) detectors in general showed equal or better performance than the heavy and voluminous NaI(Tl) detectors. The free movement of the ambulatory patient and the avoidance of cable connections to stationary data-collecting systems gave improved possibilities for measurements of the relevant parameters. From this point of view, portable CdTe(Cl) detectors must be considered an important advance for radioactivity studies in

  19. Cadmium absorption inhibitors for soil

    Energy Technology Data Exchange (ETDEWEB)

    Kitamura, S.

    1974-05-25

    Cadmium absorption by soil is one cause of soil pollution. Cadmium adsorption inhibitors were prepared by mixing alginic acid which contained brown algae (Ascophyllum nodosum) and an inorganic material, shell fossils. This mixture was highly effective in preventing cadmium absorption by the soil.

  20. Iodide kinetics and experimental I-131 therapy in a xenotransplanted human sodium-iodide symporter-transfected human follicular thyroid carcinoma cell line

    NARCIS (Netherlands)

    Smit, J.W.A.; Elst, van der J.P.; Karperien, M.; Que, I.; Stokkel, M.; Heide, van der D.; Romijn, J.A.

    2002-01-01

    Uptake of iodide is a prerequisite for radioiodide therapy in thyroid cancer. However, loss of iodide uptake is frequently observed in metastasized thyroid cancer, which may be explained by diminished expression of the human sodium-iodide symporter (hNIS). We studied whether transfection of hNIS int

  1. Methyl Iodide Formation Under Postulated Nuclear Reactor Accident Conditions

    International Nuclear Information System (INIS)

    The formation of methyl iodide under conditions of postulated nuclear reactor accidents is discussed. Although thermodynamic calculations indicate the equilibrium methyl iodide concentrations would be quite low, calculations based on a simple kinetic scheme involving reaction between small hydrocarbon species and iodine indicate that concentrations higher than equilibrium can occur during the course of the reaction. Such calculations were performed over a wide range of initial species concentrations and a range of temperatures representative of some reactor accident situations. These calculations suggest that little methyl iodide would be expected within the core volume where temperatures are maximum. As the gas leaves the core volume and expands into the plenum region, it cools and the concentration of methyl iodide increases. At the intermediate temperatures which might characterize this region, the formation of methyl iodide from thermally induced reactions could reach its maximum rate. The gas continues to cool, however, and it is probable that by the time it leaves the plenum region it has cooled to the point where thermally induced reactions may be of little importance. Although the thermally induced reactions will become slower as the gas expands and cools, the radiation-induced reactions will not be slowed to the same extent. The gases leaving the core carry fission products and hence a radiation source is available to initiate reaction by a temperature-independent process. An investigation of the radiation chemical formation and decomposition of methyl iodide in the presence of steam suggests that radiation-induced methyl iodide formation will generally be rapid under the postulated accident situations. Thus, in the plenum region where thermal reactions have become slow, the radiation-induced reaction can still proceed and may well become the dominant factor. The same situation probably pertains as well to the containment region. (author)

  2. Macrosegregation during Plane Front Solidification of Cesium Iodide wt Percent Thallium Iodide Alloy

    Science.gov (United States)

    Sidawi, Ibrahim M. S.

    Macrosegregation produced during directional solidification of CsI-1 wt% TlI by vertical Bridgman technique has been examined in crucibles of varying diameter, from 0.5 to 2.0 cm. Phase diagram and temperature dependence of the thermal conductivity have been determined. The experimentally observed liquid-solid interface shape and the fluid flow behavior have been compared with that computed from the commercially available code FIDAP. Thallium iodide content of the alloy was observed to increase along the length of the directionally solidified specimens, resulting in continuously decreasing light output. The experimentally observed solutal distribution agrees with predictions from the boundary layer model of Favier. The observed macrosegregation behavior suggests that there is a significant convection in the melt even in the smallest crucible diameter of 0.5 cm.

  3. Phase 1 Methyl Iodide Deep-Bed Adsorption Tests

    Energy Technology Data Exchange (ETDEWEB)

    Nick Soelberg; Tony Watson

    2014-08-01

    Nuclear fission results in the production of fission products (FPs) and activation products including iodine-129, which could evolve into used fuel reprocessing facility off-gas systems, and could require off-gas control to limit air emissions to levels within acceptable emission limits. Research, demonstrations, and some reprocessing plant experience have indicated that diatomic iodine can be captured with efficiencies high enough to meet regulatory requirements. Research on the capture of organic iodides has also been performed, but to a lesser extent [Jubin 2012b]. Several questions remain open regarding the capture of iodine bound in organic compounds. Deep-bed methyl iodide adsorption testing has progressed according to a multi-laboratory methyl iodide adsorption test plan. This report summarizes the first phase of methyl iodide adsorption work performed according to this test plan using the deep-bed iodine adsorption test system at the Idaho National Laboratory (INL), performed during Fiscal Year (FY) 2013 and early FY-2014. Testing has been performed to address questions posed in the test plan, and followed the testing outline in the test plan. Tests established detection limits, developed procedures for sample analysis with minimal analytical interferences, and confirmed earlier results that show that the methyl iodide reacts when in contact with the AgZ sorbent, and not significantly in the gas flow upstream of the sorbent. The reaction(s) enable separation of the iodine from the organic moiety, so that the iodine can chemisorb onto the sorbent. The organic moiety can form other compounds, some of which are organic compounds that are detected and can be tentatively identified using GC-FID and GCMS. Test results also show that other gas constituents (NOx and/or H2O) can affect the methyl iodide reactions. With NOx and H2O present in the gas stream, the majority of uncaptured iodine exiting iodine-laden sorbent beds is in the form of I2 or HI, species that

  4. Standard free energy of formation of iron iodide

    Science.gov (United States)

    Khandkar, A.; Tare, V. B.; Wagner, J. B., Jr.

    1983-01-01

    An experiment is reported where silver iodide is used to determine the standard free energy of formation of iron iodide. By using silver iodide as a solid electrolyte, a galvanic cell, Ag/AgI/Fe-FeI2, is formulated. The standard free energy of formation of AgI is known, and hence it is possible to estimate the standard free energy of formation of FeI2 by measuring the open-circuit emf of the above cell as a function of temperature. The free standard energy of formation of FeI2 determined by this method is -38784 + 24.165T cal/mol. It is estimated that the maximum error associated with this method is plus or minus 2500 cal/mol.

  5. A novel peculiar mutation in the sodium/iodide symporter gene in spanish siblings with iodide transport defect.

    Science.gov (United States)

    Kosugi, Shinji; Okamoto, Hiroomi; Tamada, Aiko; Sanchez-Franco, F

    2002-08-01

    Previously, we reported two Spanish siblings with congenital hypothyroidism due to total failure of iodide transport. These were the only cases reported to date who received long-term iodide treatment over 10 yr. We examined the sodium/iodide symporter (NIS) gene of these patients. A large deletion was observed by long and accurate PCR using primers derived from introns 2 and 7 of the NIS gene. PCR-direct sequencing revealed a deletion of 6192 bases spanning from exon 3 to intron 7 and an inverted insertion of a 431-base fragment spanning from exon 5 to intron 5 of the NIS gene. The patients were homozygous for the mutation, and their mother was heterozygous. In the mutant, deletion of exons 3-7 was suggested by analysis using programs to predict exon/intron organization, resulting in an in-frame 182-amino acid deletion from Met(142) in the fourth transmembrane domain to Gln(323) in the fourth exoplasmic loop. The mutant showed no iodide uptake activity when transfected into COS-7 cells, confirming that the mutation was the direct cause of the iodide transport defect in these patients. Further, the mutant NIS protein was synthesized, but not properly expressed, on the cell surface, but was mostly accumulated in the cytoplasm, suggesting impaired targeting to the plasma membrane. PMID:12161518

  6. Enhanced Olefin Cross Metathesis Reactions: The Copper Iodide Effect

    Science.gov (United States)

    Voigtritter, Karl; Ghorai, Subir

    2011-01-01

    Copper iodide has been shown to be an effective co-catalyst for the olefin cross metathesis reaction. In particular, it has both a catalyst stabilizing effect due to iodide ion, as well as copper(I)-based phosphine-scavenging properties that apply to use of the Grubbs-2 catalyst. A variety of Michael acceptors and olefinic partners can be cross-coupled under mild conditions in refluxing diethyl ether that avoid chlorinated solvents. This effect has also been applied to chemistry in water at room temperature using the new surfactant TPGS-750-M. PMID:21528868

  7. Mercuric iodide dosimeter response to high energy electron beams

    Energy Technology Data Exchange (ETDEWEB)

    Loewinger, E.; Nissenbaum, J.; Schieber, M.M.

    1988-01-01

    Mercuric iodide solid state dosimeter response to high energy electron beams of up to 35 MeV is reported. High sensitivity of up to 1.5 V/cGy was observed with a 200 V external bias, as well as several mV/cGy, with no external bias for small volume (approx. 10 mm/sup 3/) detectors. The physical characteristics of the detector response are discussed, showing the feasibility of mercuric iodide as a reliable dosimeter for high energy electron beams.

  8. Analysis Of The Underpotential Deposition Of Cadmium On Copper

    Directory of Open Access Journals (Sweden)

    Kowalik R.

    2015-09-01

    Full Text Available In this study the process of deposition of cadmium on polycrystalline copper electrode in sulfate solution was investigated. The process of underpotential and bulk deposition was analyzed by classical electrochemical method: cyclic voltammetry(CV, anodic stripping voltammetry(ASV and electrochemical quartz crystal microbalance(EQCM. The obtained results were compared with electrochemical impedance spectroscopy(EIS measurements. CV, EQCM and EIS results suggest that the UPD of cadmium starts below potential −0.4 V vs Ag/AgCl. Additionally the stripping analysis indicates the formation of cadmium monolayer with different density of deposited atoms depending on the applied potential. The transition from UPD to bulk deposition occurs below potential −0,7 V.

  9. Uptake of Iodide From Water in Atlantic Halibut Larvae (Hippoglossus Hippoglossus L.)

    DEFF Research Database (Denmark)

    Moren, Mari; Sloth, Jens Jørgen; Hamre, Kristin

    2008-01-01

    relative low levels of iodide (0-22 nM) and except for samples from one site; the levels of iodide and iodate were in agreement with previously published data. The uptake of iodide from seawater was measured by incubating Atlantic halibut larvae in water with a constant level of radioactive iodide (I-125...... is whether Atlantic halibut larvae are capable of absorbing iodide from the water and if so, can the seawater sustain the iodine requirement during larval development and metamorphosis. Levels of iodide and iodate in seawater samples from four different rearing facilities were analysed. All samples contained...... concentration of iodide in the water. The highest level of iodide used was 2000 nM,100 times higher than what was measured in the seawater samples. The uptake curves did not seem to reach equilibrium. This may be due to a constant nonspecific uptake or that the equilibrium level is higher than 2000 n...

  10. Cadmium in Sweden - environmental risks

    Energy Technology Data Exchange (ETDEWEB)

    Parkman, H.; Iverfeldt, Aa. [Swedish Environmental Research Inst. (Sweden); Borg, H.; Lithner, G. [Stockholm Univ. (Sweden). Inst. for Applied Environmental Research

    1998-03-01

    This report aims at assessing possible effects of cadmium in the Swedish environment. Swedish soils and soft freshwater systems are, due to a generally poor buffering capacity, severely affected by acidification. In addition, the low salinity in the Baltic Sea imply a naturally poor organism structure, with some important organisms living close to their limit of physiological tolerance. Cadmium in soils is mobilized at low pH, and the availability and toxicity of cadmium in marine systems are enhanced at low salinity. The Swedish environment is therefore extra vulnerable to cadmium pollution. The average concentrations of cadmium in the forest mor layers, agricultural soils, and fresh-waters in Sweden are enhanced compared to `back-ground concentrations`, with a general increasing trend from the north to the south-west, indicating strong impact of atmospheric deposition of cadmium originating from the central parts of Europe. In Swedish sea water, total cadmium concentrations, and the fraction of bio-available `free` cadmium, generally increases with decreasing salinity. Decreased emissions of cadmium to the environment have led to decreasing atmospheric deposition during the last decade. The net accumulation of cadmium in the forest mor layer has stopped, and even started to decrease. In northern Sweden, this is due to the decreased deposition, but in southern Sweden the main reason is increased leakage of cadmium from the topsoil as a consequence of acidification. As a result, cadmium in the Swedish environments is undergoing an extended redistribution between different soil compartments, and from the soils to the aquatic systems. 90 refs, 23 figs, 2 tabs. With 3 page summary in Swedish

  11. Cadmium Telluride-Titanium Dioxide Nanocomposite for Photodegradation of Organic Substance.

    Science.gov (United States)

    Ontam, Areeporn; Khaorapapong, Nithima; Ogawa, Makoto

    2015-12-01

    Cadmium telluride-titanium dioxide nanocomposite was prepared by hydrothermal reaction of sol-gel derived titanium dioxide and organically modified cadmium telluride. The crystallinity of titanium dioxide in the nanocomposite was higher than that of pure titanium dioxide obtained by the reaction under the same temperature and pressure conditions, showing that cadmium telluride induced the crystallization of titanium dioxide. Diffuse reflectance spectrum of the nanocomposite showed the higher absorption efficiency in the UV-visible region due to band-gap excitation of titanium dioxide. The nanocomposite significantly showed the improvement of photocatalytic activity for 4-chlorophenol with UV light.

  12. Thermochromic luminescence of copper iodide clusters: the case of phosphine ligands.

    Science.gov (United States)

    Perruchas, Sandrine; Tard, Cédric; Le Goff, Xavier F; Fargues, Alexandre; Garcia, Alain; Kahlal, Samia; Saillard, Jean-Yves; Gacoin, Thierry; Boilot, Jean-Pierre

    2011-11-01

    Three copper(I) iodide clusters coordinated by different phosphine ligands formulated [Cu(4)I(4)(PPh(3))(4)] (1), [Cu(4)I(4)(Pcpent(3))(4)] (2), and [Cu(4)I(4)(PPh(2)Pr)(4)] (3) (PPh(3) = triphenylphosphine, Pcpent(3) = tricyclopentylphosphine, and PPh(2)Pr = diphenylpropylphosphine) have been synthesized and characterized by (1)H and (31)P NMR, elemental analysis and single crystal X-ray diffraction analysis. They crystallize in different space groups, namely, monoclinic P21/c, cubic Pa ̅3, and tetragonal I ̅42m for 1, 2, and 3, respectively. The photoluminescence properties of clusters 1 and 3 show reversible luminescence thermochromism with two highly intense emission bands whose intensities are temperature dependent. In accordance to Density Functional Theory (DFT) calculations, these two emission bands have been attributed to two different transitions, a cluster centered (CC) one and a mixed XMCT/XLCT one. Cluster 2 does not exhibit luminescence variation in temperature because of the lack of the latter transition. The absorption spectra of the three clusters have been also rationalized by time dependent DFT (TDDFT) calculations. A simplified model is suggested to represent the luminescence thermochromism attributed to the two different excited states in thermal equilibrium. In contrast with the pyridine derivatives, similar excitation profiles and low activation energy for these phosphine-based clusters reflect high coupling of the two emissive states. The effect of the Cu-Cu interactions on the emission properties of these clusters is also discussed. Especially, cluster 3 with long Cu-Cu contacts exhibits a controlled thermochromic luminescence which is to our knowledge, unknown for this family of copper iodide clusters. These phosphine-based clusters appear particularly interesting for the synthesis of original emissive materials. PMID:21957984

  13. The electrosorption of tetraalkylammonium ions on silver iodide

    NARCIS (Netherlands)

    Keizer, de A.

    1981-01-01

    The object of the present investigations was to study the ef fect of the adsorption of charged organic ions on electrically charged, solid-liquid interfaces. To that end, symmetrical quater nary ammonium ions were adsorbed on a silver iodide-electrolyte interface at various surface charges. The elec

  14. Radiation-hard polycrystalline mercuric iodide semiconductor particle counters

    Energy Technology Data Exchange (ETDEWEB)

    Schieber, M. [Hebrew Univ., Jerusalem (Israel)]|[Sandia National Laboratories, Livermore Ca 94556 (United States); Zuck, A.; Melekhov, L.; Nissenbaum, J. [Hebrew Univ., Jerusalem (Israel); Turchetta, R.; Dulinski, W.; Husson, D.; Riester, J.L. [LEPSI (ULP/IN2P3), Strasbourg (France)

    1998-06-01

    Mercuric iodide polycrystalline radiation detectors, which can act as nuclear particle counters and for large area imaging devices, have been fabricated using three different methods. Response to X- and gamma rays, beta particles and to 100GeV muons, as well as radiation hardness results are briefly described. (orig.) 8 refs.

  15. Iodide volatility under condition relevant to PWR steam generator faults

    International Nuclear Information System (INIS)

    The evaluation of iodine volatility during steam generator tube rupture (SGTR) is hampered by three factors: (i) lack of suitable plant data under fault conditions, (ii) lack of experimental data (mainly due to the difficulty of performing experiments under the conditions required) and (iii) uncertainty in theoretical methods to extrapolate experimental data to the required conditions. This report summarises methods of estimating the volatility of hydrogen iodide and iodide salts at the required conditions of temperature and pressure. A thermodynamic method has been used to estimate HI volatility and the density correlation method for iodide salt volatility. It is assumed throughout that it is more conservative to predict higher volatility. Consideration is given to two explanations of experiments carried out at Oak Ridge National Laboratory (ORNL) on the influence of boric acid concentration and pH on the volatility of radioiodine ostensibly under SGTR conditions: (i) the results have been interpreted in terms of reactions involving volatility of iodide salt/ion-pairs and complexation by boric acid in the gas phase and (ii) the possibility is explored that the observed results are due to the influence of oxidation leading to the formation of much more volatile iodine species. (author)

  16. CADMIUM – ENVIRONMENTAL HAZARD

    Directory of Open Access Journals (Sweden)

    Henryka Langauer-Lewowicka

    2010-06-01

    Full Text Available The paper presents some information about current status of cadmium as an environmental health problem. Agricultural uses of phosphate fertilizers, sewage sludge and industrial uses of Cd are the major source of widespread of this metal at trace levels into the general environment and human foodstuffs. It is well known that high cadmium (Cd exposure causes renal damage, anemia, enteropathy, osteoporosis, osteomalacia, whereas the dose-response relationship at low levels exposure is less established. During the last decade an increasing number of studies have found an adverse health effects due to low environmental exposure to Cd. Many authors try to determine the relationship between Cd intake and Cd toxicity indicators, especially dealing renal tubular damage. The level of b2-microglobulin in urine is regarded as the most sensitive biomarker of renal disfunction due to low environmental Cd concentrations.

  17. Cadmium sulfite hexahydrate revisited

    Directory of Open Access Journals (Sweden)

    Sergio Baggio

    2008-07-01

    Full Text Available The present structural revision of the title compound, tetracadmium tetrasulfite hexahydrate, [Cd4(SO34(H2O5]·H2O, is a low-temperature upgrade (T = 100 K and R = 0.017 of the original room-temperature structure reported by Kiers & Vos [Cryst. Struct. Commun. (1978. 7, 399–403; T = 293 K and R = 0.080. The compound is a three-dimensional polymer with four independent cadmium centres, four sulfite anions and six water molecules, five of them coordinated to two cadmium centres and the remaining one an unbound solvent molecule which completes the asymmetric unit. There are two types of cadmium environment: CdO8 (through four chelating sulfite ligands and CdO6 (by way of six monocoordinated ligands. The former groups form planar arrays [parallel to (001 and separated by half a unit cell translation along c], made up of chains running along [110] and [overline{1}10], respectively. These chains are, in turn, interconnected both in an intraplanar as well as in an interplanar fashion by the latter CdO6 polyhedra into a tight three-dimensional framework. There is, in addition, an extensive network of hydrogen bonds, in which all 12 water H atoms act as donors and eight O atoms from all four sulfite groups and two water molecules act as acceptors.

  18. Crystal structure of catena-poly[[[bis(pyridine-4-carbothioamide-κN1)cadmium]-di-μ-thiocyanato-κ2N:S;κ2S:N] methanol disolvate

    OpenAIRE

    Tristan Neumann; Inke Jess; Christian Näther

    2016-01-01

    The asymmetric unit of the polymeric title compound, {[Cd(NCS)2(C6H6N2S)]·2CH3OH}n, consists of one cadmium(II) cation that is located on a centre of inversion as well as one thiocyanate anion, one pyridine-4-carbothioamide ligand and one methanol molecule in general positions. The CdII cations are octahedrally coordinated by the pyridine N atom of two pyridine-4-carbothioamide ligands and by the S and N atoms of four thiocyanate anions and are linked into chains along [010] by pairs of anion...

  19. FY-2015 Methyl Iodide Deep-Bed Adsorption Test Report

    Energy Technology Data Exchange (ETDEWEB)

    Soelberg, Nicholas Ray [Idaho National Lab. (INL), Idaho Falls, ID (United States); Watson, Tony Leroy [Idaho National Lab. (INL), Idaho Falls, ID (United States)

    2015-09-30

    Nuclear fission produces fission and activation products, including iodine-129, which could evolve into used fuel reprocessing facility off-gas systems, and could require off-gas control to limit air emissions to levels within acceptable emission limits. Deep-bed methyl iodide adsorption testing has continued in Fiscal Year 2015 according to a multi-laboratory methyl iodide adsorption test plan. Updates to the deep-bed test system have also been performed to enable the inclusion of evaporated HNO3 and increased NO2 concentrations in future tests. This report summarizes the result of those activities. Test results showed that iodine adsorption from gaseous methyl iodide using reduced silver zeolite (AgZ) resulted in initial iodine decontamination factors (DFs, ratios of uncontrolled and controlled total iodine levels) under 1,000 for the conditions of the long-duration test performed this year (45 ppm CH3I, 1,000 ppm each NO and NO2, very low H2O levels [3 ppm] in balance air). The mass transfer zone depth exceeded the cumulative 5-inch depth of 4 bed segments, which is deeper than the 2-4 inch depth estimated for the mass transfer zone for adsorbing I2 using AgZ in prior deep-bed tests. The maximum iodine adsorption capacity for the AgZ under the conditions of this test was 6.2% (6.2 g adsorbed I per 100 g sorbent). The maximum Ag utilization was 51%. Additional deep-bed testing and analyses are recommended to (a) expand the data base for methyl iodide adsorption and (b) provide more data for evaluating organic iodide reactions and reaction byproducts for different potential adsorption conditions.

  20. FY-2015 Methyl Iodide Deep-Bed Adsorption Test Report

    International Nuclear Information System (INIS)

    Nuclear fission produces fission and activation products, including iodine-129, which could evolve into used fuel reprocessing facility off-gas systems, and could require off-gas control to limit air emissions to levels within acceptable emission limits. Deep-bed methyl iodide adsorption testing has continued in Fiscal Year 2015 according to a multi-laboratory methyl iodide adsorption test plan. Updates to the deep-bed test system have also been performed to enable the inclusion of evaporated HNO3 and increased NO2 concentrations in future tests. This report summarizes the result of those activities. Test results showed that iodine adsorption from gaseous methyl iodide using reduced silver zeolite (AgZ) resulted in initial iodine decontamination factors (DFs, ratios of uncontrolled and controlled total iodine levels) under 1,000 for the conditions of the long-duration test performed this year (45 ppm CH3I, 1,000 ppm each NO and NO2, very low H2O levels [3 ppm] in balance air). The mass transfer zone depth exceeded the cumulative 5-inch depth of 4 bed segments, which is deeper than the 2-4 inch depth estimated for the mass transfer zone for adsorbing I2 using AgZ in prior deep-bed tests. The maximum iodine adsorption capacity for the AgZ under the conditions of this test was 6.2% (6.2 g adsorbed I per 100 g sorbent). The maximum Ag utilization was 51%. Additional deep-bed testing and analyses are recommended to (a) expand the data base for methyl iodide adsorption and (b) provide more data for evaluating organic iodide reactions and reaction byproducts for different potential adsorption conditions.

  1. Crystal structure of cis-bis{4-phenyl-1-[(3R-1,7,7-trimethyl-2-oxobicyclo[2.2.1]heptan-3-ylidene]thiosemicarbazidato-κ3O,N1,S}cadmium(II with an unknown solvent molecule

    Directory of Open Access Journals (Sweden)

    Vanessa Senna Nogueira

    2015-12-01

    Full Text Available The reaction between the racemic mixture of the camphor-4-phenylthiosemicarbazone derivative and cadmium acetate dihydrate yielded the title compound, [Cd(C17H20N3OS2]. The CdII ion is six-coordinated in a distorted octahedral environment by two deprotonated thiosemicarbazone ligands acting as an O,N,S-donor in a tridentate chelating mode, forming five-membered chelate rings. In the crystal, the molecules are connected via pairs of N—H...S and C—H...S interactions, building centrosymmetric dimers. One of the ligands is disordered in the campher unit over two sets of sites with site-occupancy factors of 0.7 and 0.3. The structure contains additional solvent molecules, which are disordered and for which no reasonable split model was found. Therefore, the data were corrected for disordered solvent using the SQUEEZE routine [Spek (2015. Acta Cryst. C71, 9–18] in PLATON. Since the disordered solvents were removed by data processing, and the number of solvent entities was a suggestion only, they were not considered in the chemical formula and subsequent chemical or crystal information.

  2. Crystal structure of cis-bis-{4-phenyl-1-[(3R)-1,7,7-tri-methyl-2-oxobi-cyclo-[2.2.1]heptan-3-ylidene]thio-semicarbazidato-κ(3) O,N (1),S}cadmium(II) with an unknown solvent mol-ecule.

    Science.gov (United States)

    Nogueira, Vanessa Senna; Bresolin, Leandro; Näther, Christian; Jess, Inke; de Oliveira, Adriano Bof

    2015-12-01

    The reaction between the racemic mixture of the camphor-4-phenyl-thio-semicarbazone derivative and cadmium acetate dihydrate yielded the title compound, [Cd(C17H20N3OS)2]. The Cd(II) ion is six-coordinated in a distorted octa-hedral environment by two deprotonated thio-semicarbazone ligands acting as an O,N,S-donor in a tridentate chelating mode, forming five-membered chelate rings. In the crystal, the mol-ecules are connected via pairs of N-H⋯S and C-H⋯S inter-actions, building centrosymmetric dimers. One of the ligands is disordered in the campher unit over two sets of sites with site-occupancy factors of 0.7 and 0.3. The structure contains additional solvent mol-ecules, which are disordered and for which no reasonable split model was found. Therefore, the data were corrected for disordered solvent using the SQUEEZE routine [Spek (2015 ▸). Acta Cryst. C71, 9-18] in PLATON. Since the disordered solvents were removed by data processing, and the number of solvent entities was a suggestion only, they were not considered in the chemical formula and subsequent chemical or crystal information. PMID:26870441

  3. Crystal structure of cis-bis­{4-phenyl-1-[(3R)-1,7,7-tri­methyl-2-oxobi­cyclo­[2.2.1]heptan-3-ylidene]thio­semicarbazidato-κ3 O,N 1,S}cadmium(II) with an unknown solvent mol­ecule

    Science.gov (United States)

    Nogueira, Vanessa Senna; Bresolin, Leandro; Näther, Christian; Jess, Inke; de Oliveira, Adriano Bof

    2015-01-01

    The reaction between the racemic mixture of the camphor-4-phenyl­thio­semicarbazone derivative and cadmium acetate dihydrate yielded the title compound, [Cd(C17H20N3OS)2]. The CdII ion is six-coordinated in a distorted octa­hedral environment by two deprotonated thio­semicarbazone ligands acting as an O,N,S-donor in a tridentate chelating mode, forming five-membered chelate rings. In the crystal, the mol­ecules are connected via pairs of N—H⋯S and C—H⋯S inter­actions, building centrosymmetric dimers. One of the ligands is disordered in the campher unit over two sets of sites with site-occupancy factors of 0.7 and 0.3. The structure contains additional solvent mol­ecules, which are disordered and for which no reasonable split model was found. Therefore, the data were corrected for disordered solvent using the SQUEEZE routine [Spek (2015 ▸). Acta Cryst. C71, 9–18] in PLATON. Since the disordered solvents were removed by data processing, and the number of solvent entities was a suggestion only, they were not considered in the chemical formula and subsequent chemical or crystal information. PMID:26870441

  4. Thermodynamic analysis of production of high purity titanium by thermal decomposition of titanium iodide

    Institute of Scientific and Technical Information of China (English)

    CHEN Xiao-hu; WANG Hua; LIU Yi-min; FANG Min

    2009-01-01

    High purity titanium was prepared by thermal decomposition of titanium iodide. The feasible synthetic route and optimum decompositon temperaure were obtained by thermodynamic analysis in the process of thermal decomposition of titanium iodide and nucleation growth theory. The temperature for the formation of titanium iodide is in the range of 800-900 K, at which a large amount of titanium iodide vapour can be obtained. The decomposition temperature of titanium iodide is in the range of 1 300-1 500 K, at which a favourable decomposition rate can be achieved. The experiment results show that the purity of the produced titanium is more than 99.995%.

  5. A novel mutation in the sodium/iodide symporter gene in the largest family with iodide transport defect.

    Science.gov (United States)

    Kosugi, S; Bhayana, S; Dean, H J

    1999-09-01

    We previously reported nine children with an autosomally recessive form of congenital hypothyroidism due to an iodide transport defect in a large Hutterite family with extensive consanguinity living in central Canada. Since the original report, we have diagnosed congenital hypothyroidism by newborn TSH screening in 9 additional children from the family. We performed direct sequencing of the PCR products of each NIS (sodium/iodide symporter) gene exon with flanking introns amplified from genomic DNA extracted from peripheral blood cells of the patients. We identified a novel NIS gene mutation, G395R (Gly395-->Arg; GGA-->AGA), in 10 patients examined in the present study. All of the parents tested were heterozygous for the mutation, suggesting that the patients were homozygous. The mutation was located in the 10th transmembrane helix. Expression experiments by transfection of the mutant NIS complimentary DNA into COS-7 cells showed no perchlorate-sensitive iodide uptake, confirming that the mutation is the direct cause of the iodide transport defect in these patients. A patient who showed an intermediate saliva/serum technetium ratio (14.0; normal, > or = 20) and was considered to have a partial or less severe defect in the previous report (IX-24) did not have a NIS gene mutation. It is now possible to use gene diagnostics of this unique NIS mutation to identify patients with congenital hypothyroidism due to an iodide transport defect in this family and to determine the carrier state of potential parents for genetic counseling and arranging rapid and early diagnosis of their infants. PMID:10487695

  6. Cadmium in blood and hypertension

    Energy Technology Data Exchange (ETDEWEB)

    Eum, Ki-Do; Lee, Mi-Sun [Department of Environmental Health, Graduate School of Public Health and Institute of Health and Environment, Seoul National University, Seoul (Korea, Republic of); Paek, Domyung [Department of Environmental Health, Graduate School of Public Health and Institute of Health and Environment, Seoul National University, Seoul (Korea, Republic of)], E-mail: paekdm@snu.ac.kr

    2008-12-15

    Objectives:: This study is to examine the effect of cadmium exposure on blood pressure in Korean general population. Methods:: The study population consisted of 958 men and 944 women who participated in the 2005 Korean National Health and Nutrition Examination Survey (KNHANES), in which blood pressure and blood cadmium were measured from each participant. Results:: The mean blood cadmium level was 1.67 {mu}g/L (median level 1.55). The prevalence of hypertension was 26.2%. The blood cadmium level was significantly higher among those subjects with hypertension than those without (mean level 1.77 versus 1.64 {mu}g/dL). After adjusting for covariates, the odds ratio of hypertension comparing the highest to the lowest tertile of cadmium in blood was 1.51 (95% confidence interval 1.13 to 2.05), and a dose-response relationship was observed. Systolic, diastolic, and mean arterial blood pressure were all positively associated with blood cadmium level, and this effect of cadmium on blood pressure was markedly stronger when the kidney function was reduced. Conclusions:: Cadmium exposures at the current level may have increased the blood pressure of Korean general population.

  7. Projectbeschrijving Cadmium-informatiepunt (CIP)

    NARCIS (Netherlands)

    Meijer PJ

    1989-01-01

    To minimize the use of cadmium the Central Government has decided to perform the purchase of products and materials within the Central Government as much as possible within the Draft Cadmium Decree. The activities to achieve this are as far as could be seen at the start of the project in june 19

  8. Projectbeschrijving Cadmium-informatiepunt (CIP)

    OpenAIRE

    Meijer PJ

    1989-01-01

    To minimize the use of cadmium the Central Government has decided to perform the purchase of products and materials within the Central Government as much as possible within the Draft Cadmium Decree. The activities to achieve this are as far as could be seen at the start of the project in june 1989, mentioned in this report.

  9. Synthesis,and X ray single crystal structure of two-dimentional CdIF based on cadmium 2-nitroidazolate%基于2-硝基咪唑镉二维CdI F材料的合成和晶体结构

    Institute of Scientific and Technical Information of China (English)

    田运齐; 陈岩; 么世岩

    2014-01-01

    Cadmium(Ⅱ) 2‐nitroimidazolate([Cd(Nim)2 ]n(CdIF‐14) is synthesized by reaction of 2‐ni‐troimidazol with cadmium nitrate under solvothermal condition and characterized by elemental analy‐sis ,FTIR ,TGA and Xray single crystal diffraction .Compared with the reported CdIFs ,CdIF‐14 demonstrates a two‐dimensional (2D) planar square‐network ,which Cd2+ (located at the centre of two mutually inversed tetrahedrons of N4 and O4 ) cations are linked by the deprotonated HNim and w hich (4 .4 .4 .4)‐topology has not yet been seen in ZIFs .%通过将2‐硝基咪唑与硝酸镉在甲醇溶剂中120℃溶剂热条件下反应,合成了1个新的[Cd(Nim)2](CdIF‐14),并对其进行了元素分析、红外光谱(FTIR)、热重分析(TGA)、X射线单晶衍射和粉末衍射(XRD)表征.与已经报道的咪唑镉配位聚合物[cadmium imidazolate framework (CdIF)]的三维结构相比,CdIF‐14呈四连接二维平面结构,为典型的(4,4)网格和(4.4.4.4)拓扑构型:Cd2+位于四连接网格的顶点由4个去质子的2‐硝基咪唑配体(分别以4个N原子配位和4个O原子弱相互作用形成相互倒置的N正四面体和O四面体)连接成正方形网格.虽然,ZIF的二维网格结构已有所报道,但是具有(4.4.4.4)拓扑的平面结构的ZIF尚未见报道,是金属咪唑配位聚合物结构中罕见的类型.

  10. Defective organification of iodide causing congenital goitrous hypothyroidism.

    Science.gov (United States)

    Ishikawa, N; Eguchi, K; Ohmori, T; Momotani, N; Nagayama, Y; Hosoya, T; Oguchi, H; Mimura, T; Kimura, S; Nagataki, S; Ito, K

    1996-01-01

    A 26-yr-old Japanese woman with congenital goitrous hypo-thyroidism and sensorineural deafness underwent a thyroidectomy. Examination of the thyroid gland revealed characteristic features of multinodular goiter. The T3 and T4 content in thyroglobulin (Tg) were 0.03 and 0.02 mol/mol Tg, respectively. Iodide incorporation into Tg, using slices of the thyroid tissue, revealed that iodide organification of thyroid tissue from our patient was markedly lower than that of normal controls. Then, guaiacol and iodide oxidation activities of thyroid peroxidase (TPO) in our patient's thyroid tissue were lower than those of normal controls (guaiacol assay: 1.92 vs. 30.0 +/- 5.7 mGU/mg protein; iodide assay: 1.1 vs. 6.6 +/- 2.8 mIU/mg protein). Lineweaver-Burk plot analysis of the oxidation rates of guaiacol and iodide indicated that this patient's TPO had a defect in the binding of guaiacol and iodide, but the coupling activity of the patient's TPO was not decreased compared with those of two normal thyroids. In this case and in control subjects, Nothern gel analysis of TPO messenger RNA from unstimulated and TSH-stimulated thyroid cells revealed a 3.2 kilobase species in the former and four distinct messenger RNA species of 4.0, 3.2, 2.1, and 1.7 kilobases in the latter. Western blot analysis of TPOs obtained from this patient and from control subjects identified the same 107 kDa protein, using antimicrosomal antibody-positive serum. We analyzed the coding sequence in the patient's TPO gene by using polymerase chain reaction technique. A single point mutation of G-->C at 1265 base pair was detected only in the TPO gene, but this point mutation does not alter the amino acid residue. It is possible that posttranslational modification such as abnormal glycosylation may occur in the TPO molecules. Furthermore, it is possible that there are differences in the tertiary structures of the TPO molecules between our patient and normal subjects. The above abnormalities of TPO molecules

  11. 29 CFR 1926.1127 - Cadmium.

    Science.gov (United States)

    2010-07-01

    ... containment of cadmium or materials containing cadmium on the site or location at which construction...) SAFETY AND HEALTH REGULATIONS FOR CONSTRUCTION Toxic and Hazardous Substances § 1926.1127 Cadmium. (a... forms, in all construction work where an employee may potentially be exposed to cadmium....

  12. Cadmium exposure in the Swedish environment

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1998-03-01

    This report gives a thorough description of cadmium in the Swedish environment. It comprises three parts: Cadmium in Sweden - environmental risks;, Cadmium in goods - contribution to environmental exposure;, and Cadmium in fertilizers, soil, crops and foods - the Swedish situation. Separate abstracts have been prepared for all three parts

  13. Cadmium in newborns

    OpenAIRE

    Eklund, Gunilla

    2003-01-01

    Cadmium (Cd) is a well-known nephrotoxic environmental contaminant but there are indications that the developing nervous system might be even more sensitive to Cd than the kidneys in adults. Infants are exposed to Cd from various formulas and infant diets and the gastrointestinal Cd uptake is believed to be higher in newborns than in adults. Cd levels monitored in infant foods ranged between 0.74 and 27.0 µg/kg. Cow's milk formulas had the lowest levels and cereal-based formulas had up to 21 ...

  14. Methyl iodide production in the ocean: Implications for climate change

    Science.gov (United States)

    Smythe-Wright, Denise; Boswell, Stephen M.; Breithaupt, Petra; Davidson, Russell D.; Dimmer, Claudia H.; Eiras Diaz, Ledicia B.

    2006-09-01

    Methyl iodide concentrations of up to 45 pmol L-1, which flux into the marine boundary layer, have been found in low latitude waters of the Atlantic and Indian oceans. These high concentrations correlate well with the abundance of Prochlorococcus, and we have confirmed the release of methyl iodide by this species in laboratory culture experiments. Extrapolating, we estimate the global ocean flux of iodine to the marine boundary layer from this single source to be 5.3 × 1011 g I yr-1, which is a large fraction of the previously estimated total global flux and the implications are far reaching. Climate prediction models suggest increases in sea surface temperature and changes in biogeographical provenances in response to global warming. Such changes are likely to increase the abundance of Prochlorococcus, and we estimate a concomitant ˜15% increase in the release of iodine species to the atmosphere. Potentially, this could help mitigate global warming.

  15. Crystal structure of catena-poly[[[bis­(pyridine-4-carbo­thio­amide-κN 1)cadmium]-di-μ-thio­cyanato-κ2 N:S;κ2 S:N] methanol disolvate

    OpenAIRE

    Neumann, Tristan; Jess, Inke; Näther, Christian

    2016-01-01

    The asymmetric unit of the polymeric title compound, {[Cd(NCS)2(C6H6N2S)]·2CH3OH} n , consists of one cadmium(II) cation that is located on a centre of inversion as well as one thio­cyanate anion, one pyridine-4-carbo­thio­amide ligand and one methanol mol­ecule in general positions. The CdII cations are octa­hedrally coordinated by the pyridine N atom of two pyridine-4-carbo­thio­amide ligands and by the S and N atoms of four thio­cyanate anions and are linked into chains along [010] by pair...

  16. New applications for the zinc iodide-osmium tetroxide technique.

    OpenAIRE

    Dağdeviren, A; ALP, H.; Ors, U

    1994-01-01

    The zinc iodide-osmium tetroxide (ZIO) fixation/staining method was applied for neurocytological studies and also to examine several other tissue samples including epidermal Langerhans cells, blood and bone marrow cells and lymphoid tissue. Although precise specificity cannot be attributed to the staining reaction, interesting staining patterns for different cell types were observed by using one of the ZIO staining solutions. The significance of ZIO positivity is briefly discussed.

  17. Heterogeneous ice nucleation on silver-iodide-like surfaces

    OpenAIRE

    Fraux, Guillaume; Doye, Jonathan P. K.

    2014-01-01

    We attempt to simulate the heterogeneous nucleation of ice at model silver-iodide surfaces and find relatively facile ice nucleation and growth at the Ag+ termi nated basal face, but never see nucleation at the I- terminated basal face or the prism and normal faces. Water molecules strongly adsorb onto the Ag+ terminate d face to give a well-ordered hexagonal ice-like bilayer that then acts as a template for further ice growth.

  18. Lead iodide perovskite light-emitting field-effect transistor

    OpenAIRE

    Chin, Xin Yu; Cortecchia, Daniele; Yin, Jun; Bruno, Annalisa; Soci, Cesare

    2015-01-01

    Despite the widespread use of solution-processable hybrid organic–inorganic perovskites in photovoltaic and light-emitting applications, determination of their intrinsic charge transport parameters has been elusive due to the variability of film preparation and history-dependent device performance. Here we show that screening effects associated to ionic transport can be effectively eliminated by lowering the operating temperature of methylammonium lead iodide perovskite (CH3NH3PbI3) field-eff...

  19. Radiative efficiency of lead iodide based perovskite solar cells

    OpenAIRE

    Kristofer Tvingstedt; Olga Malinkiewicz; Andreas Baumann; Carsten Deibel; Snaith, Henry J.; Vladimir Dyakonov; Bolink, Henk J.

    2015-01-01

    The maximum efficiency of any solar cell can be evaluated in terms of its corresponding ability to emit light. We herein determine the important figure of merit of radiative efficiency for Methylammonium Lead Iodide perovskite solar cells and, to put in context, relate it to an organic photovoltaic (OPV) model device. We evaluate the reciprocity relation between electroluminescence and photovoltaic quantum efficiency and conclude that the emission from the perovskite devices is dominated by a...

  20. Ionic transport in hybrid lead iodide perovskite solar cells

    OpenAIRE

    Eames, Christopher; Frost, Jarvist Moore; Piers R. F. Barnes; O'Regan, Brian C.; Walsh, Aron; Islam, M. Saiful

    2015-01-01

    Solar cells based on organic–inorganic halide perovskites have recently shown rapidly rising power conversion efficiencies, but exhibit unusual behaviour such as current–voltage hysteresis and a low-frequency giant dielectric response. Ionic transport has been suggested to be an important factor contributing to these effects; however, the chemical origin of this transport and the mobile species are unclear. Here, the activation energies for ionic migration in methylammonium lead iodide (CH3NH...

  1. The sodium iodide symporter: its implications for imaging and therapy

    International Nuclear Information System (INIS)

    The sodium iodide symporter (NIS) is an intrinsic plasma membrane glycoprotein that mediates the active transport of iodide in the thyroid gland and a number of extrathyroidal tissues, in particular lactating mammary gland. In addition to its key function in thyroid physiology, NIS-mediated iodide accumulation allows diagnostic thyroid scintigraphy as well as therapeutic radioiodine application in benign and malignant thyroid disease. NIS therefore represents one of the oldest targets for molecular imaging and therapy. Based on the effective administration of radioiodine that has been used for over 60 years in the management of follicular cell-derived thyroid cancer, cloning and characterization of the NIS gene has paved the way for the development of a novel cytoreductive gene therapy strategy based on targeted NIS expression in thyroidal and nonthyroidal cancer cells followed by therapeutic application of 131I or alternative radionuclides, including 188Re and 211At. In addition, the possibility of direct and non-invasive imaging of functional NIS expression by 123I- and 99mTc-scintigraphy or 124I-PET-imaging allows the application of NIS as a novel reporter gene. In conclusion, the dual role of NIS as diagnostic and therapeutic gene and the detection of extra-thyroidal endogenous NIS expression in breast cancer open promising perspectives in nuclear medicine and molecular oncology for diagnostic and therapeutic application of NIS outside the thyroid gland. (orig.)

  2. Synthesis and evaluation of iodide uptake inhibitors in thyroid gland

    International Nuclear Information System (INIS)

    This work was intended to discover small organic molecules acting as iodide uptake inhibitors in thyroid cells. These compounds can indeed be derivatized into biochemical probes for further characterization of proteins involved in iodide transport mechanisms. On the long term, these inhibitors also appear as attractive drug candidates for treatment of thyroid pathologies or radioprotection against iodine isotopes. A similar strategy was adopted for both of the two inhibitor families. First, we synthesized a chemical library of around 100 analogues; we measured their IC50 against iodide uptake in FRTL-5 cells to get structure-activity relationships. Absolute configuration of stereo-genic centers was also investigated, and a preferential stereochemistry was found to be responsible for activity. From this basis, around twenty 'second-generation' analogues were synthesized by combining fragments contributing to biological activity. Biological evaluation indicated that nine were very potent inhibitors, with IC50 ≤ 6 nM and satisfying physicochemical properties required for drug candidates. Finally, one photoactivatable biotinylated probe was developed in each family and used for photoaffinity labeling. Several specifically labeled proteins are still under identification and constitute new potential therapeutic targets. (author)

  3. Gold nanoelectrode ensembles for direct trace electroanalysis of iodide.

    Science.gov (United States)

    Pereira, Francisco C; Moretto, Ligia M; De Leo, Manuela; Zanoni, Maria V Boldrin; Ugo, Paolo

    2006-08-01

    A procedure for the standardization of ensembles of gold nanodisk electrodes (NEE) of 30 nm diameter is presented, which is based on the analytical comparison between experimental cyclic voltammograms (CV) obtained at the NEEs in diluted solutions of redox probes and CV patterns obtained by digital simulation. Possible origins of defects sometimes found in NEEs are discussed. Selected NEEs are then employed for the study of the electrochemical oxidation of iodide in acidic solutions. CV patterns display typical quasi-reversible behavior which involves associated chemical reactions between adsorbed and solution species. The main CV characteristics at the NEE compare with those observed at millimeter sized gold disk electrodes (Au-macro), apart a slight shift in E1/2 values and slightly higher peak to peak separation at the NEE. The detection limit (DL) at NEEs is 0.3 microM, which is more than one order of magnitude lower than DL at the Au-macro (4 microM). The mechanism of the electrochemical oxidation of iodide at NEEs is discussed. Finally, NEEs are applied to the direct determination of iodide at micromolar concentration levels in real samples, namely in some ophthalmic drugs and iodized table salt.

  4. Enhanced iodide sequestration by 3-biphenyl-5,6-dihydroimidazo 2,1-b thiazole in sodium/iodide sym-porter (NIS)-expressing cells

    International Nuclear Information System (INIS)

    The ability of the sodium/iodide sym-porter (NIS) to take up iodide has long provided the basis for cyto-reductive gene therapy and cancer treatment with radio-iodide. One of the major limitations of this approach is that radio-iodide retention in NIS-expressing cells is not sufficient for their destruction. We identified and characterized a small organic molecule capable of increasing iodide retention in HEK293 cells permanently transfected with human NIS cDNA (hNIS-HEK293) and in the rat thyroid-derived cell line FRTL-5. In the presence of 3-biphenyl-4'-yl-5,6-dihydroimidazo[2,1-b)thiazole (ISA1), the transmembrane iodide concentration gradient was increased up to 4.5-fold. Our experiments indicate that the imidazo-thiazole derivative acts either by inhibiting anion efflux mechanisms, or by promoting the relocation of iodide into subcellular compartments. This new compound is not only an attractive chemical tool to investigate the mechanisms of iodide flux at the cellular level, but also opens promising perspectives in the treatment of cancer after NIS gene transfer. (authors)

  5. Enhanced iodide sequestration by 3-biphenyl-5,6-dihydroimidazo 2,1-b thiazole in sodium/iodide sym-porter (NIS)-expressing cells

    Energy Technology Data Exchange (ETDEWEB)

    Lecat-Guillet, N.; Ambroise, Y. [CEA, DSV, Dept Bioorgan Chem andt IsotopLabelling, Inst Biol and Technol, iBiTecS, F-91191 Gif Sur Yvette (France)

    2008-07-01

    The ability of the sodium/iodide sym-porter (NIS) to take up iodide has long provided the basis for cyto-reductive gene therapy and cancer treatment with radio-iodide. One of the major limitations of this approach is that radio-iodide retention in NIS-expressing cells is not sufficient for their destruction. We identified and characterized a small organic molecule capable of increasing iodide retention in HEK293 cells permanently transfected with human NIS cDNA (hNIS-HEK293) and in the rat thyroid-derived cell line FRTL-5. In the presence of 3-biphenyl-4'-yl-5,6-dihydroimidazo[2,1-b)thiazole (ISA1), the transmembrane iodide concentration gradient was increased up to 4.5-fold. Our experiments indicate that the imidazo-thiazole derivative acts either by inhibiting anion efflux mechanisms, or by promoting the relocation of iodide into subcellular compartments. This new compound is not only an attractive chemical tool to investigate the mechanisms of iodide flux at the cellular level, but also opens promising perspectives in the treatment of cancer after NIS gene transfer. (authors)

  6. Cadmium immobilization by hydroxyapatite

    Directory of Open Access Journals (Sweden)

    Smičiklas Ivana D.

    2003-01-01

    Full Text Available The contamination of air, soil and water by cadmium is a great environmental problem. If cadmium occurs in nature in ionic form, soluble in water, it easily enters into the food chain. Hydroxyapatite (HAP, Ca-o(POAe(OH2 is a sparingly soluble salt and an excellent matrix for the removal of heavy metals from solutions. Considerable research attention has been paid to the bond between Cc/2+ ions and synthetic hydroxyapatite of known composition. The sorption mechanism is complex. The dominant process is ion exchange, but surface adsorption, surface complexation and coprecipitation can also contribute to the overall mechanism. The sorption capacity depends on the characteristics of hydroxyapatite itself and on the experimental conditions. Under optimum conditions a maximum capacity of 0.8 mol Cd2+/mol HAP can be achieved. HAP is a potential sorbent for the remediation of contaminated water and soil, for industrial waste treatment, and it is also referenced as a material that can be used as a barrier around waste depositories.

  7. Controlled cadmium telluride thin films for solar cell applications (emerging materials systems for solar cell applications). Quarterly progress report No. 1, April 9-July 8, 1979

    Energy Technology Data Exchange (ETDEWEB)

    Vedam, K.

    1979-08-01

    Preparation and properties of cadmium telluride thin films for use in solar cells are studied. CdTe sputter deposition, crystal doping, and carrier typing are discussed. Future experimental plans are described. (WHK)

  8. Electrochemistry of silver iodide the capacity of the double layer at the silver iodide-water interface

    NARCIS (Netherlands)

    Lyklema, J.; Overbeek, J.Th.G.

    1961-01-01

    A method is described for obtaining differential double layer capacities on silver iodide. Especially the influence of the nature and concentration of indifferent electrolytes was investigated, viz., the nitrates of Li·, K·, Rb·, NH4·, H·, Tl·, Mg··, Ba··, Co··, Cd··, Pb··, La···, Th····, the fluori

  9. Electron–Rotor Interaction in Organic–Inorganic Lead Iodide Perovskites Discovered by Isotope Effects

    Energy Technology Data Exchange (ETDEWEB)

    Gong, Jue; Yang, Mengjin; Ma, Xiangchao; Schaller, Richard D.; Liu, Gang; Kong, Lingping; Yang, Ye; Beard, Matthew C.; Lesslie, Michael; Dai, Ying; Huang, Baibiao; Zhu, Kai; Xu, Tao

    2016-08-04

    We report on the carrier-rotor coupling effect in perovskite organic-inorganic hybrid lead iodide (CH3NH3PbI3) compounds discovered by isotope effects. Deuterated organic-inorganic perovskite compounds including CH3ND3PbI3, CD3NH3PbI3, and CD3ND3PbI3 were synthesized. Devices made from regular CH3NH3PbI3 and deuterated CH3ND3PbI3 exhibit comparable performance in band gap, current-voltage, carrier mobility, and power conversion efficiency. However, a time-resolved photoluminescence (TRPL) study reveals that CH3NH3PbI3 exhibits notably longer carrier lifetime than that of CH3ND3PbI3, in both thin-film and single-crystal formats. Furthermore, the comparison in carrier lifetime between CD3NH3PbI3 and CH3ND3PbI3 single crystals suggests that vibrational modes in methylammonium (MA+) have little impact on carrier lifetime. In contrast, the fully deuterated compound CD3ND3PbI3 reconfirmed the trend of decreasing carrier lifetime upon the increasing moment of inertia of cationic MA+. Polaron model elucidates the electron-rotor interaction.

  10. Crystal structure of a new hybrid compound based on an iodido-plumbate(II) anionic motif.

    Science.gov (United States)

    Mokhnache, Oualid; Boughzala, Habib

    2016-01-01

    Crystals of the one-dimensional organic-inorganic lead iodide-based compound catena-poly[bis-(piperazine-1,4-diium) [[tetra-iodido-plumbate(II)]-μ-iodido] iodide monohydrate], (C4N2H12)2[PbI5]I·H2O, were obtained by slow evaporation at room temperature of a solution containing lead iodide and piperazine in a 1:2 molar ratio. Inorganic lead iodide chains, organic (C4N2H12)(2+) cations, water mol-ecules of crystallization and isolated I(-) anions are connected through N-H⋯·I, N-H⋯OW and OW-H⋯I hydrogen-bond inter-actions. Zigzag chains of corner-sharing [PbI6](4-) octa-hedra with composition [PbI4/1I2/2](3-) running parallel to the a axis are present in the structure packing.

  11. Synthesis, Characterization, Crystal Structure, and Biological Studies of a Cadmium(II Complex with a Tridentate Ligand 4′-Chloro-2,2′:6′,2′′-Terpyridine

    Directory of Open Access Journals (Sweden)

    L. A. Saghatforoush

    2011-01-01

    Full Text Available A new Cd(II complex with the ligand 4′-chloro-2,2′6′,2′′-terpyridine (Cltpy, [Cd(Cltpy(I2], has been synthesized and characterized by CHN elemental analysis, 1H-NMR, 13C-NMR, and IR spectroscopy and structurally analyzed by X-ray single-crystal diffraction. The single-crystal X-ray analyses show that the coordination number in complex is five with three terpyridine (Cltpy N-donor atoms and two iodine atoms. The antibacterial activities of Cltpy and its Cd(II complex are tested against different bacteria.

  12. Cadmium(2) complexes of cytosine

    International Nuclear Information System (INIS)

    Complexes of cadmium(2) with cytosine obtained from aqueous or physiological solutions at room temperature are reported. The complexes were characterized by spectroscopic, conductometric, 1H-NMR, and 13C-NMR measurements and also by thermogravimetry. (Authors)

  13. Discovery of the Cadmium Isotopes

    OpenAIRE

    Amos, S.; Thoennessen, M

    2009-01-01

    Thirty-seven cadmium isotopes have so far been observed; the discovery of these isotopes is discussed. For each isotope a brief summary of the first refereed publication, including the production and identification method, is presented.

  14. Cadmium telluride nuclear radiation detectors

    International Nuclear Information System (INIS)

    The characteristics and performance of undoped high resistivity cadmium telluride detectors are compared to chlorine lifted counters. It is shown, in particular, that Undodep CdTe is in fact aluminium doped and that compensation occurs, as an silicon or germanium, by pair and triplet formation between the group III donor and the doubly charged cadmium vacancy acceptor. Furthermore, in chlorine doped samples, the polarization effect results from the unpaired level at Esub(c)-0,6eV

  15. Speciation of Dissolved Cadmium

    DEFF Research Database (Denmark)

    Holm, Peter Engelund; Andersen, Sjur; Christensen, Thomas Højlund

    1995-01-01

    ) method separates dissolved Cd into free divalent Cd (Cd 2+) and complexed Cd and furthermore separates the latter into the operationally defined forms: labile, slowly labile and stable complexes. The dialysis (ED) method determines high molecular weight Cd complexes (above 1000mol. wt). For both methods...... the reproducibility was good. By combining the results of the GEOCHEM calculations in terms of the inorganic complexes, and the IE results, the fractions of free and inorganically complexed Cd were estimated. The IE and ED results furthermore provided information about the organic complexes. Selected environmental......Equilibrium dialysis and ion exchange methods, as well as computer calculations (GEOCHEM), were applied for speciation of dissolved cadmium (Cd) in test solutions and leachate samples. The leachate samples originated from soil, compost, landfill waste and industrial waste. The ion exchange (IE...

  16. Abiotic formation of methyl iodide on synthetic birnessite: A mechanistic study

    Energy Technology Data Exchange (ETDEWEB)

    Allard, Sébastien, E-mail: s.allard@curtin.edu.au; Gallard, Hervé

    2013-10-01

    Methyl iodide is a well-known volatile halogenated organic compound that contributes to the iodine content in the troposphere, potentially resulting in damage to the ozone layer. Most methyl iodide sources derive from biological activity in oceans and soils with very few abiotic mechanisms proposed in the literature. In this study we report that synthetic manganese oxide (birnessite δ-MnO{sub 2}) can catalyze the formation of methyl iodide in the presence of natural organic matter (NOM) and iodide. Methyl iodide formation was only observed at acidic pH (4–5) where iodide is oxidized to iodine and NOM is adsorbed on δ-MnO{sub 2}. The effect of δ-MnO{sub 2}, iodide and NOM concentrations, nature of NOM and ionic strength was investigated. High concentrations of methyl iodide were formed in experiments conducted with the model compound pyruvate. The Lewis acid property of δ-MnO{sub 2} leads to a polarization of the iodine molecule, and catalyzes the reaction with natural organic matter. As manganese oxides are strong oxidants and are ubiquitous in the environment, this mechanism could significantly contribute to the global atmospheric input of iodine. Highlights: • Methyl iodide is formed when iodide, natural organic matter and MnO{sub 2} are in contact. • Iodide is oxidized to iodine by MnO{sub 2} which reacts with NOM already adsorbed on MnO{sub 2}. • High formation of methyl iodide was observed with pyruvate. • This abiotic mechanism could contribute to the input of iodine in the atmosphere. • This abiotic mechanism could impact the ozone layer in the troposphere.

  17. Abiotic formation of methyl iodide on synthetic birnessite: A mechanistic study

    International Nuclear Information System (INIS)

    Methyl iodide is a well-known volatile halogenated organic compound that contributes to the iodine content in the troposphere, potentially resulting in damage to the ozone layer. Most methyl iodide sources derive from biological activity in oceans and soils with very few abiotic mechanisms proposed in the literature. In this study we report that synthetic manganese oxide (birnessite δ-MnO2) can catalyze the formation of methyl iodide in the presence of natural organic matter (NOM) and iodide. Methyl iodide formation was only observed at acidic pH (4–5) where iodide is oxidized to iodine and NOM is adsorbed on δ-MnO2. The effect of δ-MnO2, iodide and NOM concentrations, nature of NOM and ionic strength was investigated. High concentrations of methyl iodide were formed in experiments conducted with the model compound pyruvate. The Lewis acid property of δ-MnO2 leads to a polarization of the iodine molecule, and catalyzes the reaction with natural organic matter. As manganese oxides are strong oxidants and are ubiquitous in the environment, this mechanism could significantly contribute to the global atmospheric input of iodine. Highlights: • Methyl iodide is formed when iodide, natural organic matter and MnO2 are in contact. • Iodide is oxidized to iodine by MnO2 which reacts with NOM already adsorbed on MnO2. • High formation of methyl iodide was observed with pyruvate. • This abiotic mechanism could contribute to the input of iodine in the atmosphere. • This abiotic mechanism could impact the ozone layer in the troposphere

  18. Crystal structure of catena-poly[[[bis(pyridine-4-carbothioamide-κN1cadmium]-di-μ-thiocyanato-κ2N:S;κ2S:N] methanol disolvate

    Directory of Open Access Journals (Sweden)

    Tristan Neumann

    2016-03-01

    Full Text Available The asymmetric unit of the polymeric title compound, {[Cd(NCS2(C6H6N2S]·2CH3OH}n, consists of one cadmium(II cation that is located on a centre of inversion as well as one thiocyanate anion, one pyridine-4-carbothioamide ligand and one methanol molecule in general positions. The CdII cations are octahedrally coordinated by the pyridine N atom of two pyridine-4-carbothioamide ligands and by the S and N atoms of four thiocyanate anions and are linked into chains along [010] by pairs of anionic ligands. These chains are further linked into layers extending along (201 by intermolecular N—H...O and O—H...S hydrogen bonds. One of the amino H atoms of the pyridine-4-carbothioamide ligand is hydrogen-bonded to the O atom of a methanol molecule, and a symmetry-related methanol molecule is the donor group to the S atom of another pyridine-4-carbothioamide ligand whereby each of the pyridine-4-carbothioamide ligands forms two pairs of centrosymmetric N—H...S and O—H...S hydrogen bonds. The methanol molecules are equally disordered over two orientations.

  19. Femtosecond laser ablation of cadmium tungstate for scintillator arrays

    Science.gov (United States)

    Richards, S.; Baker, M. A.; Wilson, M. D.; Lohstroh, A.; Seller, P.

    2016-08-01

    Ultrafast pulsed laser ablation has been investigated as a technique to machine CdWO4 single crystal scintillator and segment it into small blocks with the aim of fabricating a 2D high energy X-ray imaging array. Cadmium tungstate (CdWO4) is a brittle transparent scintillator used for the detection of high energy X-rays and γ-rays. A 6 W Yb:KGW Pharos-SP pulsed laser of wavelength 1028 nm was used with a tuneable pulse duration of 10 ps to 190 fs, repetition rate of up to 600 kHz and pulse energies of up to 1 mJ was employed. The effect of varying the pulse duration, pulse energy, pulse overlap and scan pattern on the laser induced damage to the crystals was investigated. A pulse duration of ≥500 fs was found to induce substantial cracking in the material. The laser induced damage was minimised using the following operating parameters: a pulse duration of 190 fs, fluence of 15.3 J cm-2 and employing a serpentine scan pattern with a normalised pulse overlap of 0.8. The surface of the ablated surfaces was studied using scanning electron microscopy, energy dispersive X-ray spectroscopy, atomic force microscopy and X-ray photoelectron spectroscopy. Ablation products were found to contain cadmium tungstate together with different cadmium and tungsten oxides. These laser ablation products could be removed using an ammonium hydroxide treatment.

  20. Expression of sodium-iodide symporter in thyroid gland tumors: immunohistochemical study

    Directory of Open Access Journals (Sweden)

    Bondarenko O.O.

    2009-01-01

    Full Text Available One of the key moments of radioiodine therapy, and also radioisotope diagnostics of cancers of a thyroid gland is ability of their cells to accumulate iodide. This ability is provided with activity of the specific transporter – sodium-iodide symporter. Our research has shown disorders of sodium-iodide symporter immunoexpression in all tumors of thyroid gland: from overexpression and absence of plasma membrane expression in differentiated carcinomas, up to weak or actually absent in low differentiated cancers and Hurtle-cells tumors. Thus, there is a prospect of application of the sodium-iodide symporter, as the prognostic marker of thyroid cancers.

  1. Temperature dependent energy levels of methylammonium lead iodide perovskite

    Energy Technology Data Exchange (ETDEWEB)

    Foley, Benjamin J.; Marlowe, Daniel L.; Choi, Joshua J., E-mail: jjc6z@virginia.edu, E-mail: mgupta@virginia.edu, E-mail: scudiero@wsu.edu [Department of Chemical Engineering, University of Virginia, Charlottesville, Virginia 22904 (United States); Sun, Keye; Gupta, Mool C., E-mail: jjc6z@virginia.edu, E-mail: mgupta@virginia.edu, E-mail: scudiero@wsu.edu [Department of Electrical and Computer Engineering, University of Virginia, Charlottesville, Virginia 22904 (United States); Saidi, Wissam A. [Department of Mechanical Engineering and Materials Science, University of Pittsburgh, Pittsburgh, Pennsylvania 15261 (United States); Scudiero, Louis, E-mail: jjc6z@virginia.edu, E-mail: mgupta@virginia.edu, E-mail: scudiero@wsu.edu [Chemistry Department and Materials Science and Engineering Program, Washington State University, Pullman, Washington 99164 (United States)

    2015-06-15

    Temperature dependent energy levels of methylammonium lead iodide are investigated using a combination of ultraviolet photoemission spectroscopy and optical spectroscopy. Our results show that the valence band maximum and conduction band minimum shift down in energy by 110 meV and 77 meV as temperature increases from 28 °C to 85 °C. Density functional theory calculations using slab structures show that the decreased orbital splitting due to thermal expansion is a major contribution to the experimentally observed shift in energy levels. Our results have implications for solar cell performance under operating conditions with continued sunlight exposure and increased temperature.

  2. Persistent photovoltage in methylammonium lead iodide perovskite solar cells

    OpenAIRE

    Baumann, A.; Tvingstedt, K.; Heiber, M. C.; Väth, S.; C. Momblona; H. J. Bolink; Dyakonov, V.

    2014-01-01

    We herein perform open circuit voltage decay (OCVD) measurements on methylammonium lead iodide (CH3NH3PbI3) perovskite solar cells to increase the understanding of the charge carrier recombination dynamics in this emerging technology. Optically pulsed OCVD measurements are conducted on CH3NH3PbI3 solar cells and compared to results from another type of thin-film photovoltaics, namely, the two reference polymer–fullerene bulk heterojunction solar cell devices based on P3HT:PC60BM and PTB7:PC70...

  3. Temperature dependent energy levels of methylammonium lead iodide perovskite

    International Nuclear Information System (INIS)

    Temperature dependent energy levels of methylammonium lead iodide are investigated using a combination of ultraviolet photoemission spectroscopy and optical spectroscopy. Our results show that the valence band maximum and conduction band minimum shift down in energy by 110 meV and 77 meV as temperature increases from 28 °C to 85 °C. Density functional theory calculations using slab structures show that the decreased orbital splitting due to thermal expansion is a major contribution to the experimentally observed shift in energy levels. Our results have implications for solar cell performance under operating conditions with continued sunlight exposure and increased temperature

  4. Measuring Cell Death by Propidium Iodide Uptake and Flow Cytometry.

    Science.gov (United States)

    Crowley, Lisa C; Scott, Adrian P; Marfell, Brooke J; Boughaba, Jeanne A; Chojnowski, Grace; Waterhouse, Nigel J

    2016-01-01

    Propidium iodide (PI) is a small fluorescent molecule that binds to DNA but cannot passively traverse into cells that possess an intact plasma membrane. PI uptake versus exclusion can be used to discriminate dead cells, in which plasma membranes become permeable regardless of the mechanism of death, from live cells with intact membranes. PI is excited by wavelengths between 400 and 600 nm and emits light between 600 and 700 nm, and is therefore compatible with lasers and photodetectors commonly available in flow cytometers. This protocol for PI staining can be used to quantitate cell death in most modern research facilities and universities. PMID:27371595

  5. Polarized spectral complexes of optical functions of monovalent mercury iodide

    Science.gov (United States)

    Sobolev, V. V.; Sobolev, V. Val.; Anisimov, D. V.

    2015-12-01

    Spectral complexes of optical functions of monovalent mercury iodide Hg2I2 were determined for E ⊥ c and E || c polarizations in the range from 2 to 5.5 eV at 4.2 K. The permittivity and characteristic electron energy loss spectra were expanded in simple components with the determination of their main parameters, including the energy of the maximum and the oscillator strength. The calculations were performed based on known reflectance spectra. Computer programs based on Kramers-Kronig relations and the improved parameter-free method of Argand diagrams were used.

  6. Electronic properties and Compton profiles of silver iodide

    Indian Academy of Sciences (India)

    Alpa Dashora; Ambica Marwal; K R Soni; B L Ahuja

    2010-06-01

    We have carried out an extensive study of electronic properties of silver iodide in - and -phases. The theoretical Compton profiles, energy bands, density of states and anisotropies in momentum densities are computed using density functional theories. We have also employed full-potential linearized augmented plane-wave method to derive the energy bands and the density of states. To compare our theoretical data, isotropic Compton profile measurement on -AgI using 137Cs Compton spectrometer at an intermediate resolution of 0.38 a.u. has been undertaken. The theoretical anisotropies are also interpreted on the basis of energy bands.

  7. Exploring the crystallization landscape of cadmium bis(N-hydroxyethyl, N-isopropyldithiocarbamate), Cd[S{sub 2}CN(iPr)CH{sub 2}CH{sub 2}OH]{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Tan, Yee Seng; Halim, Siti Nadiah Abdul [Malaya Univ., Kuala Lumpur (Malaysia). Dept. of Chemistry; Tiekink, Edward R.T. [Malaya Univ., Kuala Lumpur (Malaysia). Dept. of Chemistry; Sunway Univ., Bandar Sunway (Malaysia). Centre for Chemical Crystallography

    2016-04-01

    Crystallization of Cd[S{sub 2}CN(iPr)CH{sub 2}CH{sub 2}OH]{sub 2} from ethanol yields the coordination polymer [{Cd[S_2CN(iPr)CH_2CH_2OH]_2}.EtOH]{sub ∞} (1) within 3 h. When the solution is allowed to stand for another hour, the needles begin to dissolve and prisms emerge of the supramolecular isomer (SI), binuclear {Cd[S_2CN(iPr)CH_2CH_2OH]_2}{sub 2}.2EtOH (2). These have been fully characterized spectroscopically and by X-ray crystallography. Polymeric 1 has 2-fold symmetry and features dithiocarbamate ligands coordinating two octahedral Cd atoms in a μ{sub 2}κ{sup 2}-tridentate mode. Binuclear 2 is centrosymmetric with two ligands being μ{sub 2}κ{sup 2}-tridentate as for 1 but the other two being κ{sup 2}-chelating leading to square pyramidal geometries. The conversion of the kinetic crystallization product, 1, to thermodynamic 2 is irreversible but transformations mediated by recrystallization (ethanol and acetonitrile) to related literature SI species, namely coordination polymer [{Cd[S_2CN(iPr)CH_2CH_2OH]_2}{sub 3}.MeCN]{sub ∞} and binuclear {Cd[S_2CN(iPr)CH_2CH_2OH]_2}{sub 2}.2H{sub 2}O.2MeCN, are demonstrated, some of which are reversible. Three other crystallization outcomes are described whereby crystal structures were obtained for the 1:2 co-crystal {Cd[S_2CN(iPr)CH_2CH_2OH]_2}{sub 2}:2[3-(propan-2-yl)-1,3-oxazolidine-2-thione] (3), the salt co-crystal [iPrNH{sub 2}(CH{sub 2}CH{sub 2}OH)]{sub 4}[SO{sub 4}]{sub 2}{Cd[S_2CN(iPr)CH_2CH_2OH]_2}{sub 2} (4) and the salt [iPrNH{sub 2}(CH{sub 2}CH{sub 2}OH)]{Cd[S_2CN(iPr)CH_2CH_2OH]_3} (5). These arise as a result of decomposition/oxidation of the dithiocarbamate ligands. In each of 3 and 4 the binuclear {Cd[S_2CN(iPr)CH_2CH_2OH]_2}{sub 2} SI, as in 2, is observed strongly suggesting a thermodynamic preference for this form.

  8. Physiological characterization of cadmium-exposed Chlamydomonas reinhardtii.

    Science.gov (United States)

    Bräutigam, Anja; Schaumlöffel, Dirk; Preud'homme, Hugues; Thondorf, Iris; Wesenberg, Dirk

    2011-12-01

    Chlamydomonas reinhardtii is a common model organism for investigation of metal stress. This green alga produces phytochelatins in the presence of metal ions. The influence of cadmium is of main interest, because it is a strong activator of phytochelatin synthase. Cell wall bound and intracellular cadmium content was determined after exposition to 70 µm CdCl(2), showing the main portion of the metal outside the cell. Nevertheless, imported cadmium was sufficient to cause significant changes in thiolpeptide metabolism and its transcriptional regulation. Modern analytical approaches enable new insights into phytochelatin (PC) distribution. A new rapid and precise UPLC-MS method allowed high-throughput PC quantification in algal samples after 1, 4, 24 and 48 h cadmium stress. Initially, canonic PCs were synthesized in C. reinhardtii during cadmium exposition, but afterwards CysPCs became the major thiolpeptides. Thus, after 48 h the concentration of the PC-isoforms CysPC(2-3) and CysGSH attained between 105 and 199 nmol g(-1) fresh weight (FW), whereas the PC(2-3) concentrations were only 15 nmol g(-1) FW. The relative quantification of γ-glutamyl transpeptidase (γ-GT) mRNA suggests the generation of CysPCs by glutamate cleavage from canonic PCs by γ-GT. Furthermore, a homology model of C. reinhardtii phytochelatin synthase was constructed to verify the use of crystal structures from Anabaena sp. phytochelatin synthase (PCS) for docking studies with canonical PCs and CysPCs. From the difference in energy scores, we hypothesize that CysPC may prevent the synthesis of canonical PCs by blocking the binding pocket. Finally, possible physiological reasons for the high abundance of CysPC compared with their canonic precursors are discussed.

  9. Purification, crystallization and halide phasing of a Streptococcus agalactiae backbone pilin GBS80 fragment

    OpenAIRE

    Vengadesan, Krishnan; Ma, Xin; Dwivedi, Prabhat; Ton-That, Hung; Narayana, Sthanam V. L

    2010-01-01

    The C-terminal fragment of Streptococcus agalactiae (group B streptococcus) major (backbone) pilin GBS80 was purified and crystallized in two different space groups. Single-wavelength anomalous dispersion (SAD) data collected to 2.0 Å resolution on a iodide (NaI) derivative crystal using the home source were used to obtain initial phases.

  10. Solubility in aqueous system of potassium sulfate, cadmium sulfate at 50 deg C

    International Nuclear Information System (INIS)

    Solubility in system potassium sulfate-cadmium sulfate-water at 50 deg C is studied using isothermal method. Crystallization limits of K2SO4, CdSO4x8/3H2O double salt 2K2SO4x2CdSO4x3H2O at 50 deg C are determined

  11. Zinc-induced protection against cadmium

    Energy Technology Data Exchange (ETDEWEB)

    Early, J.L.; Schnell, R.C.

    1978-02-01

    Pretreatment of male rats with cadmium acetate potentiates the duration of hexobarbital hypnosis and inhibits the rate of hepatic microsomal drug metabolism. Pretreatment of rats with zinc acetate protects against these alterations in drug action elicited by cadmium.

  12. Growth, surface treatment and characterization of polycrystalline lead iodide thick films prepared using close space deposition technique

    Science.gov (United States)

    Zhu, Xinghua; Sun, Hui; Yang, Dingyu; Zheng, Xiaolin

    2012-11-01

    Lead iodide (PbI2) polycrystalline thick films were fabricated on glass substrates with a conductive indium-tin-oxide layer using a close space deposition technique. The morphology of the as-deposited PbI2 films is typically and highly oriented polycrystalline structure, made up of microcrystal platelets upright on the substrate plane. Two techniques including the surface mechanical cutting and after-growth cadmium telluride coating were employed to improve the films' surface properties. It was shown that both of the film surface treatment methods markedly decreased the dark current of PbI2 films. The photo-to-dark current ratio of about 2.05 under 241Am γ-ray source with activity of 2.78 μCi irradiation was obtained from the film treated using both surface cutting and after-growth CdTe coating. Charge transport characteristics of these films were measured and the hole mobility 7.7×10-2-1.67×10-1 cm2/V s was estimated.

  13. Progress in tumor therapy with human sodium iodide symporter

    International Nuclear Information System (INIS)

    The sodium iodide symporter (NIS) is an intrinsic plasma membrane protein that mediates active iodide transport into the thyroid gland and several extrathyroidal tissues, in particular the lactation mammary gland. Because of the cloning characterization of NIS, its key role in thyroid pathology and physiology could be investigated. The progress would be significant if the mechanisms of NIS expression in lactating mammary gland and breast cancer are elucidated, in which more than 80% of cases express endogenous NIS. In the future, two approaches could extend the use of radioiodide treatment to thyroid cancer and nonthyroidal cancer. One is by using the main mechanisms involving tumorous transformation to treat the tumor, based on the reinducing NIS expression in thyroid and cancer. The other is based on the application of NIS as a novel cytoreductive gene therapy strategy. NIS offers the unique advantage that it can be used both as a reporter and as a therapeutic gene, so that it is possible to image, monitor, and treat the tumor with radioiodide, just as in differentiated thyroid cancer. (authors)

  14. Nuclear detonation, thyroid cancer and potassium iodide prophylaxis

    Directory of Open Access Journals (Sweden)

    Viroj Wiwanitkit

    2011-01-01

    Full Text Available The recent nuclear disaster at Japan has raised global concerns about effects of radioactive leakage in the environment, associated hazards, and how they can be prevented. In this article, we have tried to explain about the guidelines laid down by World Health Organization for a potassium iodide prophylaxis following a nuclear disaster, and its mechanism of action in preventing thyroid cancer. Data was collected mainly from the studies carried out during the Chernobyl disaster of Russia in 1986 and the hazardous effects especially on the thyroid gland were studied. It was seen that radioactive iodine leakage from the nuclear plants mainly affected the thyroid gland, and especially children were at a higher risk at developing the cancers. Potassium Iodide prophylaxis can be administered in order to prevent an increase in the incidence of thyroid cancers in the population of an area affected by a nuclear disaster. However, one has to be cautious while giving it, as using it without indication has its own risks.

  15. Numerical modelling of methyl iodide in the eastern tropical Atlantic

    Directory of Open Access Journals (Sweden)

    I. Stemmler

    2013-06-01

    Full Text Available Methyl iodide (CH3I is a volatile organic halogen compound that contributes significantly to the transport of iodine from the ocean to the atmosphere, where it plays an important role in tropospheric chemistry. CH3I is naturally produced and occurs in the global ocean. The processes involved in the formation of CH3I, however, are not fully understood. In fact, there is an ongoing debate whether production by phytoplankton or photochemical degradation of organic matter is the main source term. Here, both the biological and photochemical production mechanisms are considered in a biogeochemical module that is coupled to a one-dimensional water column model for the eastern tropical Atlantic. The model is able to reproduce observed subsurface maxima of CH3I concentrations. But, the dominating source process cannot be clearly identified as subsurface maxima can occur due to both direct biological and photochemical production. However, good agreement between the observed and simulated difference between surface and subsurface methyl iodide concentrations is achieved only when direct biological production is taken into account. Production rates for the biological CH3I source that were derived from published laboratory studies are shown to be inappropriate for explaining CH3I concentrations in the eastern tropical Atlantic.

  16. Bioavailability of cadmium from linseed and cocoa

    DEFF Research Database (Denmark)

    Hansen, Max; Sloth, Jens Jørgen; Rasmussen, Rie Romme

    In Denmark and EU the exposure of cadmium from food is at a level that is relatively close to the Tolerable Daily Intake (TDI). This report describes an investigation of the bioavailability of cadmium in selected food items known to contain high levels of cadmium. The purpose was to provide data ...... or crushed linseed nor the intake of cocoa and chocolate....

  17. Mechanisms of cadmium carcinogenesis

    International Nuclear Information System (INIS)

    Cadmium (Cd), a heavy metal of considerable occupational and environmental concern, has been classified as a human carcinogen by the International Agency for Research on Cancer (IARC). The carcinogenic potential of Cd as well as the mechanisms underlying carcinogenesis following exposure to Cd has been studied using in vitro cell culture and in vivo animal models. Exposure of cells to Cd results in their transformation. Administration of Cd in animals results in tumors of multiple organs/tissues. Also, a causal relationship has been noticed between exposure to Cd and the incidence of lung cancer in human. It has been demonstrated that Cd induces cancer by multiple mechanisms and the most important among them are aberrant gene expression, inhibition of DNA damage repair, induction of oxidative stress, and inhibition of apoptosis. The available evidence indicates that, perhaps, oxidative stress plays a central role in Cd carcinogenesis because of its involvement in Cd-induced aberrant gene expression, inhibition of DNA damage repair, and apoptosis.

  18. CuI-catalyzed Synthesis of Aryl Thiocyanates from Aryl Iodides

    Institute of Scientific and Technical Information of China (English)

    Ye Feng WANG; Yuan ZHOU; Jia Rui WANG; Lei LIU; Qing Xiang GUO

    2006-01-01

    An operationally simple and inexpensive catalyst system was developed for the cross coupling of potassium thiocyanate with aryl iodides by using CuI as catalyst, 1, 10-phenanthroline as ligand, and tetraethylammonium iodide as activator. The procedure is applicable for the synthesis of diverse aryl thiocyanates without any exotic, poisonous reagents.

  19. Bibenzimidazole containing mixed ligand cobalt(III) complex as a selective receptor for iodide

    Digital Repository Service at National Institute of Oceanography (India)

    Indumathy, R.; Parameswarana, P.S.; Aiswarya, C.V.; Nair, B.U.

    -, OH- and OAc- do not bring about any dramatic visual colorimetric changes. However, metallo-receptor 2 brings about vivid color change with iodide anion visually and this could be due to charge transfer transition via ion pair formation with iodide ion...

  20. Crystal structure of catena-poly[[(3-tert-butyl­pyridine-κN)(4-tert-butyl­pyridine-κN)cadmium]-di-μ-thio­cyanato-κ2 N:S;κ2 S:N

    OpenAIRE

    Werner, Julia; Reinert, Thorben; Jess, Inke; Näther, Christian

    2014-01-01

    In the crystal structure of the title compound, [Cd(NCS)2(C9H13N)2] n , the CdII cations are coordinated in a slightly distorted octa­hedral geometry by one 3-tert-butyl­pyridine ligand, one 4-tert-butyl­pyridine ligand and two pairs of translationally-equivalent μ-1,3-bridging thio­cyanate ligands, all of which are in general positions. These μ-1,3-bridging thio­cyante anions bridge the CdII cations, forming chains that propagate parallel to the b axis.

  1. Crystal structure of catena-poly[[(3-tert-butylpyridine-κN)(4-tert-butylpyridine-κN)cadmium]-di-μ-thiocyanato-κ2N:S;κ2S:N

    OpenAIRE

    Julia Werner; Thorben Reinert; Inke Jess; Christian Näther

    2014-01-01

    In the crystal structure of the title compound, [Cd(NCS)2(C9H13N)2]n, the CdII cations are coordinated in a slightly distorted octahedral geometry by one 3-tert-butylpyridine ligand, one 4-tert-butylpyridine ligand and two pairs of translationally-equivalent μ-1,3-bridging thiocyanate ligands, all of which are in general positions. These μ-1,3-bridging thiocyante anions bridge the CdII cations, forming chains that propagate parallel to the b axis.

  2. The influence of different growth procedures on the suitability of cadmium crystals as nuclear radiation detectors. Einfluss unterschiedlicher Zuechtungsverfahren auf die Eignung von Cadmiumtellurid-Kristallen als Kernstrahlungs-Detektoren

    Energy Technology Data Exchange (ETDEWEB)

    Marquardt, H.

    1991-07-04

    CdTe crystals which are suitable to serve as detectors and had been produced with different methods were subjected to tests: THM-material (compensation with Cl-10{sup 19} atoms/cm{sup 3} CdTe); (2) Bridgman material; (3) Sublimation material. Results: THM has almost reached international standards (Eurorad-detector). Bridgman material is very good for low cost production of counters (without spectral resolution) in large numbers. CdTe remains the most promising candidate for {gamma}-detectors at room temperature. (HP).

  3. Phonon density of states of cadmium iodide deduced from the fine structure of the 3A2g → 1Eg electronic transition of nickel(2+) ion-doped cadmium iodide.

    NARCIS (Netherlands)

    Kuindersma, S. R.; Boudewijn, Pieter Reinder

    1978-01-01

    The absorption and MCD spectra of the 3A2g → 1Eg transition of CdI2:Ni2+ at ∼ 12,500 cm-1 were measured. The unusual vibronic fine structure is explained by the coupling of the phonons of the CdI2 lattice to the electronic states of Ni2+. The dispersion curves for the acoustical and optical branches

  4. Structures, Phase Transitions and Tricritical Behavior of the Hybrid Perovskite Methyl Ammonium Lead Iodide

    Science.gov (United States)

    Whitfield, P. S.; Herron, N.; Guise, W. E.; Page, K.; Cheng, Y. Q.; Milas, I.; Crawford, M. K.

    2016-01-01

    We have examined the crystal structures and structural phase transitions of the deuterated, partially deuterated and hydrogenous organic-inorganic hybrid perovskite methyl ammonium lead iodide (MAPbI3) using time-of-flight neutron and synchrotron X-ray powder diffraction. Near 330 K the high temperature cubic phases transformed to a body-centered tetragonal phase. The variation of the order parameter Q for this transition scaled with temperature T as Q ∼ (Tc−T)β, where Tc is the critical temperature and the exponent β was close to ¼, as predicted for a tricritical phase transition. However, we also observed coexistence of the cubic and tetragonal phases over a range of temperature in all cases, demonstrating that the phase transition was in fact first-order, although still very close to tricritical. Upon cooling further, all the tetragonal phases transformed into a low temperature orthorhombic phase around 160 K, again via a first-order phase transition. Based upon these results, we discuss the impact of the structural phase transitions upon photovoltaic performance of MAPbI3 based solar cells. PMID:27767049

  5. 2,3,5-Triphenyl-2H-tetrazol-3-ium iodide

    Directory of Open Access Journals (Sweden)

    Hoong-Kun Fun

    2012-09-01

    Full Text Available The asymmetric unit of the title molecular salt, C19H15N4+·I−, contains four 2,3,5-triphenyl-2H-tetrazol-3-ium cations and five iodide anions, with two of the latter lying on crystallographic inversion centres. In each cation, the tetrazole ring is essentially planar (r.m.s. deviations = 0.004–0.007 Å. The dihedral angles between the tetrazole ring and its three attached benzene rings in the four independent cations are: 12.9 (4, 67.0 (4, 48.1 (4; 20.8 (4, 51.1 (4, 62.3 (4; 11.4 (4, 52.3 (4, 47.3 (4 and 6.0 (4, 85.7 (4, 43.5 (4°. A C—H...I hydrogen bond and C—H...π interactions are observed in the crystal.

  6. Fabrication of Efficient Low-Bandgap Perovskite Solar Cells by Combining Formamidinium Tin Iodide with Methylammonium Lead Iodide

    Energy Technology Data Exchange (ETDEWEB)

    Liao, Weiqiang; Zhao, Dewei; Yu, Yue; Shrestha, Niraj; Ghimire, Kiran; Grice, Corey R.; Wang, Changlei; Xiao, Yuqing; Cimaroli, Alexander J.; Ellingson, Randy J.; Podraza, Nikolas J.; Zhu, Kai; Xiong, Ren-Gen; Yan, Yanfa

    2016-09-28

    Mixed tin (Sn)-lead (Pb) perovskites with high Sn content exhibit low bandgaps suitable for fabricating the bottom cell of perovskite-based tandem solar cells. In this work, we report on the fabrication of efficient mixed Sn-Pb perovskite solar cells using precursors combining formamidinium tin iodide (FASnI3) and methylammonium lead iodide (MAPbI3). The best-performing cell fabricated using a (FASnI3)0.6(MAPbI3)0.4 absorber with an absorption edge of ~1.2 eV achieved a power conversion efficiency (PCE) of 15.08 (15.00)% with an open-circuit voltage of 0.795 (0.799) V, a short-circuit current density of 26.86(26.82) mA/cm2, and a fill factor of 70.6(70.0)% when measured under forward (reverse) voltage scan. The average PCE of 50 cells we have fabricated is 14.39 +/- 0.33%, indicating good reproducibility.

  7. Colorimetric sensing of iodide based on triazole-acetamide functionalized gold nanoparticles

    International Nuclear Information System (INIS)

    We have modified gold nanoparticles (AuNPs) with triazole acetamide to obtain a material for the sensitive and selective colorimetric determination of iodide. The functionalized AuNPs were prepared by a reductive single chemical step using a Cu(I)-catalyzed click reaction. The presence of iodide ions induces the aggregation of these AuNPs and results in a color change from wine-red to purple. The iodide-induced aggregation can be detected visually with bare eyes, but also by photometry. The detection limit is as low as 15 nM. The method displays excellent selectivity for iodide over other anions due to the selective interaction with the amido groups of the triazole. The method was applied to the determination of iodide in spiked lake waters. (author)

  8. Growth and study of mixed crystals of Ca–Cd iodate

    Indian Academy of Sciences (India)

    S L Garud; K B Saraf

    2008-08-01

    Mixed crystals of calcium–cadmium iodate were grown by a simple gel technique using diffusion method. The optimum conditions were established by varying various parameters such as pH of gel solution, gel concentration, gel setting time, concentration of reactants etc. Crystals having different morphologies and habits were obtained. Prismatic, dendritic crystals of calcium–cadmium iodate and prismatic needle shaped, hopper crystals of mixed iodate were obtained. Some of them were transparent, some transluscent and a few others were opaque. The crystals were characterized using FT–IR, EDAX, XRD, TGA and DTA.

  9. Polarization and Dielectric Study of Methylammonium Lead Iodide Thin Film to Reveal its Nonferroelectric Nature under Solar Cell Operating Conditions

    Energy Technology Data Exchange (ETDEWEB)

    Hoque, Md Nadim Ferdous; Yang, Mengjin; Li, Zhen; Islam, Nazifah; Pan, Xuan; Zhu, Kai; Fan, Zhaoyang

    2016-07-08

    Researchers have debated whether methylammonium lead iodide (MAPbI3), with a perovskite crystal structure, is ferroelectric and therefore contributes to the current--voltage hysteresis commonly observed in hybrid perovskite solar cells (PSCs). We thoroughly investigated temperature-dependent polarization, dielectric, and impedance spectroscopies, and we found no evidence of ferroelectric effect in a MAPbI3 thin film at normal operating conditions. Therefore, the effect does not contribute to the hysteresis in PSCs, whereas the large component of ionic migration observed may play a critical role. Our temperature-based polarization and dielectric studies find that MAPbI3 exhibits different electrical behaviors below and above ca. 45 degrees C, suggesting a phase transition around this temperature. In particular, we report the activation energies of ionic migration for the two phases and temperature-dependent permittivity of MAPbI3. This study contributes to the understanding of the material properties and device performance of hybrid perovskites.

  10. Oral cadmium chloride intoxication in mice

    DEFF Research Database (Denmark)

    Andersen, O; Nielsen, J B; Svendsen, P

    1988-01-01

    Diethyldithiocarbamate (DDC) is known to alleviate acute toxicity due to injection of cadmium salts. However, when cadmium chloride was administered by the oral route, DDC enhanced rather than alleviated the acute toxicity; both oral and intraperitoneal (i.p.) administration of DDC had this effect....... Thus, orally administered DDC enhanced cadmium-induced duodenal and ileal tissue damage and inhibition of peristalsis, as indicated by an increased intestinal transit time. At low cadmium doses, the whole-body retention of cadmium was increased by oral DDC administration. Intraperitoneally administered...

  11. The fabrication of sub-micron size cesium iodide x-ray scintillator

    Science.gov (United States)

    Hun, Chien Wan; Chen, Po Chun; Huang, Ker Jer; Chen, Chien Chon

    2015-05-01

    The cesium iodide (CsI) scintillator can converts incident X-ray into visible light with very high conversion efficiency of optical photons. The incident energy, response time, film thickness, sample size, and spatial resolution require in engineering and medical applications are difference. A smooth and flat surface and single crystal structure of CsI enhance the X-ray to visible light conversion. However, the regular CsI is soft and extremely hygroscopic; it is very difficult to polish to obtain a smooth and optical flat plane. In order to obtain a good quality of CsI scintillator for X-ray application we used an ordering channel as template and formed sub-micron CsI wire in the template. The fabrication process including: (1) Ordering structure of nano or sub-micron channels were made by an anodization method; (2) fill CsI scintillated film on the channel by CsI solution, (3) fill CsI melt into the channel formation single crystal of sub-micron crystalline scintillator after solidification. The non-vacuum processes of anodization and solidication methods were used for the sub-micron CsI scintillator column formation that is cost down the scintillator fabrication. In addition, through the fabrication method, the ordering structure scintillator of scintillator can be made by anodic treatment and die casting technology with low cost and rapid production; moreover, the film oxidized metal tubes of the tubular template can be further manufactured to nano tubes by adjusting electrolyte composition, electrolysis voltage, and processing time of anodic treatment, and the aperture size, the thickness and the vessel density of the nano tube can be controlled and ranged from 10 nm to 500 nm, 0.1 μm to 1000 μm, and hundred million to thousand billion tube/cm2, respectively.

  12. (2S,7S-10-Ethyl-1,8,10,12-tetraazatetracyclo[8.3.1.18,12.02,7]pentadecan-10-ium iodide

    Directory of Open Access Journals (Sweden)

    Augusto Rivera

    2012-10-01

    Full Text Available The title chiral quaternary ammonium salt, C13H25N4+·I−, was synthesized through the Menschutkin reaction between the cage aminal (2S,7S-1,8,10,12-tetraazatetracyclo[8.3.1.18,12.02,7]pentadecane and ethyl iodide. The quaternization occurred regioselectively on the nitrogen with major sp3 character. The crystal structure consists of anions and cations separated by normal distances. Ions are not linked through C—H...I hydrogen bonds.

  13. Arsenic-cadmium interaction in rats.

    Science.gov (United States)

    Díaz-Barriga, F; Llamas, E; Mejía, J J; Carrizales, L; Santoyo, M E; Vega-Vega, L; Yáñez, L

    1990-11-01

    Simultaneous exposure to cadmium and arsenic is highly probable in the urban area of San Luis Potosi, Mexico due to common localization of copper and zinc smelters. Therefore, in this work, rats were intraperitoneally exposed either to cadmium or arsenic alone, or simultaneously to both metals. The effects of these treatments on three different toxicological parameters were studied. Cadmium modified the LD50 of arsenic and conversely arsenic modified the LD50 for cadmium. At the histopathological level, arsenic appeared to protect against the cadmium effects, especially on testes. This protective effect seemed to be related to the glutathione levels found in this tissue: rats exposed to both arsenic and cadmium, presented glutathione values intermediate to those observed after exposure to either metal alone; arsenic had the highest value and cadmium the lowest. In liver, rats exposed to arsenic, cadmium or arsenic and cadmium, presented glutathione values below those in the saline group, with the lowest value corresponding to the arsenic and cadmium treatment. The results appear to support the proposed interaction between arsenic and cadmium and coexposure to both metals seems to alter certain effects produced by either metal alone. PMID:2219140

  14. Determination of cadmium in biological samples.

    Science.gov (United States)

    Klotz, Katrin; Weistenhöfer, Wobbeke; Drexler, Hans

    2013-01-01

    Analyses of cadmium concentrations in biological material are performed using inductively coupled plasma mass spectrometry (ICP-MS) and atomic absorption spectrometry (AAS), but also electrochemical methods, neutron activation analysis (NAA), and X-ray fluorescence spectrometry (XRF). The predominant sample matrices include blood, plasma, serum, and urine, as well as hair, saliva, and tissue of kidney cortex, lung, and liver. While cadmium in blood reveals rather the recent exposure situation, cadmium in urine reflects the body burden and is an indicator for the cumulative long term exposure.After chronic exposure, cadmium accumulates in the human body and causes kidney diseases, especially lesions of proximal tubular cells. A tubular proteinuria causes an increase in urinary excretion of microproteins. Excretions of retinol binding protein (RBP), β2-microglobulin (β2-M), and α1-microglobulin are validated biomarkers for analyzing cadmium effects. For this purpose, immunological procedures such as ELISA, and radio- and latex-immunoassays are used.However, proteinuria is not specific to cadmium, but can also occur after exposure to other nephrotoxic agents or due to various kidney diseases. In summary, cadmium in urine and blood are the most specific biomarkers of cadmium exposure. A combination of parameters of exposure (cadmium in blood, cadmium in urine) and parameters of effect (e.g., β2-M, RBP) is required to reveal cadmium-induced nephrological effects. PMID:23430771

  15. Insulin Expression in Rats Exposed to Cadmium

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Objectives To investigate the effects of cadmium exposure on insulin expression in rats. Methods Eighteen adult SD assessed. The levels of cadmium and zinc in pancreas, blood and urine glucose, serum insulin and urine NAG (N-acyetyl-β-glucosaminidase) were determined. The gene expressions of metallothionein (MT) and insulin were also measured,and the oral glucose tolerance tests (OGTT) were carried out. Results The contents of cadmium in pancreas in cadmium-treated rats were higher than that in the control group, which was associated with slight increase of zinc in pancreas.not change significantly after cadmium administration, and the UNAG had no change in Cd-treated group. The gene expression the change of the expression of insulin, MT-Ⅰ and MT-Ⅱ genes. Cadmium can influence the biosynthesis of insulin, but does not induce the release of insulin. The dysfunction of pancreas occurs earlier than that of kidney after administration of cadmium.

  16. Strawberry growers wavered over methyl iodide, feared public backlash

    Directory of Open Access Journals (Sweden)

    Julie Guthman

    2016-08-01

    Full Text Available Methyl iodide, once promoted as a suitable alternative to methyl bromide for soil fumigation in strawberry systems, was withdrawn from the market in 2012 after a contentious regulatory battle that revolved around its high toxicity. At the time of its withdrawal, Arysta LifeScience, the maker of the chemical, claimed that it was no longer economically viable. In this study, I investigated what made the chemical nonviable, with a specific focus on growers' nonadoption of it. Interviews with strawberry growers in the four top California strawberry-growing counties revealed that growers' decisions not to use it were primarily related to public disapproval, although the continued availability of methyl bromide and other fumigants played a contributing role by making adoption less urgent. The study results suggest that policies in place during the methyl bromide phaseout did not strongly encourage the development and extension of less toxic alternatives, which undermined the strawberry industry's position.

  17. Betaine potassium iodide dihydrate: a new compound of betaine

    International Nuclear Information System (INIS)

    Betaine potassium iodide dihydrate, [(CH3)3N+CH2COO-]2.KI.2H2O, BKI for short, is a new compound of the aminoacid betaine with a triclinic symmetry and the space group P1-bar at room temperature. The study of dielectric properties provided evidence for the existence of a structural phase transition occurring around 100 K. The spontaneous electric polarization is zero in both phases. A study of dielectric dispersion disclosed two relaxational modes with different relevance in the high and in the low temperature phases. The main features observed in BKI are consistently described by the Landau theory, by assuming a quadratic coupling between the primary order parameter and the electric polarization. (author). Letter-to-the-editor

  18. Photon recycling in lead iodide perovskite solar cells

    Science.gov (United States)

    Pazos-Outón, Luis M.; Szumilo, Monika; Lamboll, Robin; Richter, Johannes M.; Crespo-Quesada, Micaela; Abdi-Jalebi, Mojtaba; Beeson, Harry J.; Vrućinić, Milan; Alsari, Mejd; Snaith, Henry J.; Ehrler, Bruno; Friend, Richard H.; Deschler, Felix

    2016-03-01

    Lead-halide perovskites have emerged as high-performance photovoltaic materials. We mapped the propagation of photogenerated luminescence and charges from a local photoexcitation spot in thin films of lead tri-iodide perovskites. We observed light emission at distances of ≥50 micrometers and found that the peak of the internal photon spectrum red-shifts from 765 to ≥800 nanometers. We used a lateral-contact solar cell with selective electron- and hole-collecting contacts and observed that charge extraction for photoexcitation >50 micrometers away from the contacts arose from repeated recycling between photons and electron-hole pairs. Thus, energy transport is not limited by diffusive charge transport but can occur over long distances through multiple absorption-diffusion-emission events. This process creates high excitation densities within the perovskite layer and allows high open-circuit voltages.

  19. Development of mercuric iodide detectors for XAS and XRD measurements

    International Nuclear Information System (INIS)

    A prototype element for an energy dispersive detector (EDD) array was constructed using a Mercuric Iodide detector. Both detector and front end FET could be thermoelectrically cooled. Tested at SSRL, the detector had 250 eV electronic noise and 315 eV resolution at 5.9 keV. K line fluorescence spectra were collected for selected elements between Cl (2622 eV) and Zn (8638 eV). Count rate capability to 60,000 cps was demonstrated. Several detector parameters were measured, including energy linearity, resolution vs. shaping time, and detector dead time. An EXAFS (extended x-ray absorption fine structure) spectrum was recorded and compared to simultaneously collected transmission data

  20. Radiochemical extraction and separation of Cadmium(II) and mercury(II) with bis-2-ethylhexyl sulphoxide

    International Nuclear Information System (INIS)

    The extraction of cadmium(II) and mercury(II) from iodide solutions has been investigated by tracer techniques with bis-2-ethylhexyl sulphoxide (B2EHSO) in benzene as an extractant. For comparison, extraction studies also have been carried out with a well-known neutral organophosphorus extractant, trioctylphosphine oxide (TOPO). The extraction data have been analyzed by both graphical and theoretical methods taking into account aqueous phase speciation and all plausible complexes extracted into the organic phase. The results demonstrate that Cd(II) is extracted as CdI2 . 2 B2EHSO with B2EHSO and CdI2 . 2 TOPO with TOPO. In the case of Hg(II) the extracted species are HgI2, HgI2 . B2EHSO/TOPO and HgI2 . 2 B2EHSO/2 TOPO. These results also demonstrate the mutual separation possibility of cadmium and mercury from iodide solutions using B2EHSO or TOPO as an extractant. (orig.)

  1. Incorporation of iodine into apatite structure: a crystal chemistry approach using Artificial Neural Network

    Directory of Open Access Journals (Sweden)

    Jianwei eWang

    2015-06-01

    Full Text Available Materials with apatite crystal structure provide a great potential for incorporating the long-lived radioactive iodine isotope (129I in the form of iodide (I- from nuclear waste streams. Because of its durability and potentially high iodine content, the apatite waste form can reduce iodine release rate and minimize the waste volume. Crystal structure and composition of apatite was investigated for iodide incorporation into the channel of the structure using Artificial Neural Network. A total of 86 experimentally determined apatite crystal structures of different compositions were compiled from literature, and 46 of them were used to train the networks and 42 were used to test the performance of the trained networks. The results show that the performances of the networks are satisfactory for predictions of unit cell parameters a and c and channel size of the structure. The trained and tested networks were then used to predict unknown compositions of apatite that incorporates iodide. With a crystal chemistry consideration, chemical compositions that lead to matching the size of the structural channel to the size of iodide were then predicted to be able to incorporate iodide in the structural channel. The calculations suggest that combinations of A site cations of Ag+, K+, Sr2+, Pb2+, Ba2+, and Cs+, and X site cations, mostly formed tetrahedron, of Mn5+, As5+, Cr5+, V5+, Mo5+, Si4+, Ge4+, and Re7+ are possible apatite compositions that are able to incorporate iodide. The charge balance of different apatite compositions can be achieved by multiple substitutions at a single site or coupled substitutions at both A and X sites. The results give important clues for designing experiments to synthesize new apatite compositions and also provide a fundamental understanding how iodide is incorporated in the apatite structure. This understanding can provide important insights for apatite waste forms design by optimizing the chemical composition and synthesis

  2. Crystal structures of tetramethylammonium (2,2′-bipyridinetetracyanidoferrate(III trihydrate and poly[[(2,2′-bipyridine-κ2N,N′di-μ2-cyanido-dicyanido(μ-ethylenediamine(ethylenediamine-κ2N,N′cadmium(IIiron(II] monohydrate

    Directory of Open Access Journals (Sweden)

    Songwuit Chanthee

    2016-05-01

    Full Text Available The crystal structures of the building block tetramethylammonium (2,2′-bipyridine-κ2N,N′tetracyanidoferrate(III trihydrate, [N(CH34][Fe(CN4(C10H8N2]·3H2O, (I, and a new two-dimensional cyanide-bridged bimetallic coordination polymer, poly[[(2,2′-bipyridine-κ2N,N′di-μ2-cyanido-dicyanido(μ-ethylenediamine-κ2N:N′(ethylenediamine-κ2N,N′cadmium(IIiron(II] monohydrate], [CdFe(CN4(C10H8N2(C2H8N22]·H2O, (II, are reported. In the crystal of (I, pairs of [Fe(2,2′-bipy(CN4]− units (2,2′-bipy is 2,2′-bipyridine are linked together through π–π stacking between the pyridyl rings of the 2,2′-bipy ligands to form a graphite-like structure parallel to the ab plane. The three independent water molecules are hydrogen-bonded alternately with each other, forming a ladder chain structure with R44(8 and R66(12 graph-set ring motifs, while the disordered [N(CH34]+ cations lie above and below the water chains, and the packing is stabilized by weak C—H...O hydrogen bonds. The water chains are further linked with adjacent sheets into a three-dimensional network via O—H...O hydrogen bonds involving the lattice water molecules and the N atoms of terminal cyanide groups of the [Fe(2,2′-bipy(CN4]− building blocks, forming an R44(12 ring motif. Compound (II features a two-dimensional {[Fe(2,2′-bipy(CN4Cd(en2]}n layer structure (en is ethylenediamine extending parallel to (010 and constructed from {[Fe(2,2′-bipy(CN4Cd(en]}n chains interlinked by bridging en ligands at the Cd atoms. Classical O—H...N and N—H...O hydrogen bonds involving the lattice water molecule and N atoms of terminal cyanide groups and the N—H groups of the en ligands are observed within the layers. The layers are further connected via π–π stacking interactions between adjacent pyridine rings of the 2,2′-bipy ligands, completing a three-dimensional supramolecular structure.

  3. Evaluation of quaternary ammonium halides for removal of methyl iodide from flowing air streams

    International Nuclear Information System (INIS)

    The quaternary ammonium halides of several tertiary amines were used as impregnants on activated carbon and were tested for methyl iodide penetration in accordance with test Method A, ASTM D3803, 1979, ''Standard Test Methods for Radio-iodine Testing of Nuclear Grade Gas Phase Adsorbents''. The results suggest that the primary removal mechanism for methyl iodide-131 is isotopic exchange with the quaternary ammonium halide. For example, a 5 wt% impregnation of each of the tetramethyl, tetraethyl, tetrapropyl and tetrabutyl ammonium iodides on activated carbon yielded percent penetrations of 0.47, 0.53, 0.78, and 0.08 respectively when tested according to Method A of ASTM D3803. A sample impregnated with 5% tetramethyl ammonium hydroxide gave a methyl iodide penetration of 64.87%, thus supporting the isotopic exchange mechanism for removal. It has been a generally held belief that the success of tertiary amines as impregnants for radioiodine removal is a result of their ability to complex with the methyl iodide. The results of the work indicates that the superiority of the tertiary amines similar to triethylene diamine and quinuclidine, when compared to their straight chain analogs, is a result of their ease in reacting with methyl iodide-127 to form the quaternary ammonium iodide followed by isotopic exchange

  4. A two-dimensional cadmium(II) polymer based on nicotinic acid and thiocyanate ligands.

    Science.gov (United States)

    Zhou, Lin; Wang, Hui-Ting

    2015-09-01

    A cadmium-thiocyanate complex, poly[[bis(nicotinic acid-κN)di-μ-thiocyanato-κ(2)N:S;κ(2)S:N-cadmium(II)] monohydrate], {[Cd(NCS)2(C6H5NO2)2]·H2O}n, was synthesized by the reaction of nicotinic acid, cadmium nitrate tetrahydrate and potassium thiocyanide in aqueous solution. In the crystal structure, each Cd(II) cation is in a distorted octahedral coordination environment, coordinated by the N and S atoms of nicotinic acid and thiocyanate ligands. Neighbouring Cd(II) cations are linked together by thiocyanate bridges to form a two-dimensional network. Hydrogen-bond interactions between the uncoordinated solvent water molecules and the organic ligands result in the formation of the three-dimensional supramolecular network. PMID:26322616

  5. Syntheses, Crystal Structures and Fluorescence of Cadmium(Ⅱ) Coordination Polymers with Pyrazine-1,4-dioxide, 2-Methylpyrazine-1,4-dioxide and Thiocyanate as Mixed Bridge Ligands

    Institute of Scientific and Technical Information of China (English)

    SHI Jing-Min; ZHANG Feng-Xia; ZHANG Xia; XU Hai-Yan; LIU Lian-Dong; MA Jian-Ping

    2006-01-01

    Two Cd(Ⅱ) coordination polymers have been synthesized with pyrazine-1,4-dioxide(L1), 2-methylpyrazine-1,4-dioxide (L2), and thiocyanate anion as mixed bridge ligands. Crystal data for complex 1 [Cd(μ13-SCN-)2(L1)]n: monoclinic system, space group P21/n with a =6.8342(11), b = 14.349(2), c = 10.5443(16) (A), β = 98.534(2)°, V = 1022.5(3) (A)3, Z = 4,C6H4CdN4O2S2, Mr = 340.65, Dc. = 2.213 g/cm3, F(000) = 656 andμ = 2.527 mm-1; and those for2: triclinic system, space group P1 with a = 7.877(3), b = 8.693(3), c = 8.754(3) (A), α =102.297(6), β= 102.464(6), γ= 98.480(6)°, V = 560.0(3) (A)3, Z = 2, C7H6CdN4O2S2, Mr = 354.68,Dc = 2.103 g/cm3, F(000) = 344 and μ = 2.311 mm-1. 1 shows a three-dimensional network structure, and along the c direction a one-dimensional chain is constructed by the coordination of Cd(Ⅱ) ions withμ1,3-SCN- ligands, and the L1 bridging ligands made the chains connect each other leading to the formation of a three-dimensional structure. For 2, the one-dimensional chains along the b axis are generated by the coordination of L2 bridging ligands with Cd(Ⅱ) ions, and the chains are further joined byμ1,3-SCN- bridging ligands forming a two-dimensional sheet structure on the (1 0 -1) plane. Both complexes 1 and 2 exhibit strong fluorescence emission.

  6. Crystal structure of the salt bis(triethanolamine-κ4N,O,O′,O′′cadmium bis[2-(2-oxo-2,3-dihydro-1,3-benzothiazol-3-ylacetate

    Directory of Open Access Journals (Sweden)

    Jamshid Mengnorovich Ashurov

    2016-04-01

    Full Text Available The reaction of 2-(2-oxo-2,3-dihydro-1,3-benzothiazol-3-ylacetic acid (NBTA and triethanolamine (TEA with Cd(CH3OO2 resulted in the formation of the title salt, [Cd(C6H15NO32](C9H6NO3S2. In its crystal structure, the complex cation [Cd(TEA2]2+ and two independent NBTA− units with essentially similar geometries and conformations are present. In the complex cation, each TEA molecule behaves as an N,O,O′,O′′-tetradentate ligand, giving rise to an eight-coordinate CdII ion with a bicapped trigonal–prismatic configuration. All ethanol groups of each TEA molecule form three five-membered chelate rings around the CdII ion. The Cd—O and Cd—N distances are in the ranges 2.392 (2–2.478 (2 and 2.465 (2–2.475 (3 Å, respectively. O—H...O hydrogen bonds between the TEA hydroxy groups and carboxylate O atoms connect cationic and anionic moieties into chains parallel to [110]. Each NBTA− anion is additionally linked to a symmetry-related anion through π–π stacking interactions between the benzene and thiazoline rings [minimum centroid-to-centroid separation = 3.604 (2 Å]. Together with additional C—H...O interactions, these establish a double-layer polymeric network parallel to (001.

  7. Cathodoluminescence in doped CdP2 and CdSiP2 crystals

    International Nuclear Information System (INIS)

    Some general features of the behaviour of Cu, Zn, Bi, and Mn impurities in CdSiP2 and CdP2 crystals are studied by analyzing electron beam-excited luminescence spectra measured in a temperature range of 6 to 300 K, as well as by determining their electrical parameters. The impurities are established to substitute mainly the cadmium in the crystalline lattice and to promote the formation of complexes of defects, which are radiative recombination centers. Cadmium vacancies as well participate in the defect complex formation processes. A radiation ascribed to interstitial cadmium-type defects, is discovered in CdSiP2 crystals. (author)

  8. Apoptosis and necroptosis are induced in rainbow trout cell lines exposed to cadmium

    Energy Technology Data Exchange (ETDEWEB)

    Krumschnabel, Gerhard, E-mail: Gerhard.Krumschnabel@i-med.ac.at [Division of Developmental Immunology, Biocenter, Medical University Innsbruck, Fritz-Preglstr. 3, Innsbruck (Austria); Ebner, Hannes L.; Hess, Michael W. [Division of Histology and Embryology, Medical University Innsbruck, Innsbruck (Austria); Villunger, Andreas [Division of Developmental Immunology, Biocenter, Medical University Innsbruck, Fritz-Preglstr. 3, Innsbruck (Austria)

    2010-08-01

    Cadmium is an important environmental toxicant that can kill cells. A number of studies have implicated apoptosis as well as necrosis and, most recently, a form of programmed necrosis termed necroptosis in the process of cadmium-mediated toxicity, but the exact mechanism remains ill-defined and may depend on the affected cell type. This study investigated which mode of cell death may be responsible for cell death induction in cadmium-exposed trout cell lines from gill and liver and if this cell death was sensitive to inhibitors of necroptosis or apoptosis, respectively. It was observed that intermediate levels of cadmium that killed approximately 50% of the cells over 96-120 h of exposure caused cell death that morphologically resembled apoptosis and was associated with an increase of apoptotic markers such as the number of cells with diminished DNA content (sub-G1 cells), condensed or fragmented nuclei, and elevation of caspase-3 activity. At the same time, however, cells also lost plasma membrane integrity, as indicated by uptake of propidium iodide, showed a decrease of ATP levels and mitochondrial membrane potential, and displayed cell swelling, signs associated with secondary necrosis, or equally possible, necroptotic cell death. Importantly, many of these alterations were at least partly inhibited by the necroptosis inhibitor necrostatin-1 and were to a lesser extent also sensitive to the pan-caspase inhibitor zVAD-fmk, indicating that multiple modes of cell death are concurrently induced in cadmium-exposed trout cells, including necroptosis and apoptosis. Cell death appeared to lack concurrent radical formation, consistent with genetically regulated necroptotic cell death, but was characterized by the rapid induction of DNA damage markers, and the early onset of disintegration of the Golgi complex. Comparative experiments evaluating copper-toxicity indicated that in comparison to cadmium much higher concentrations of this metal were required to induce cell

  9. Cadmium detoxification processes in the digestive gland of cephalopods in relation to accumulated cadmium concentrations

    OpenAIRE

    Bustamante, Paco; Cosson, Richard; Gallien, Isabelle; Caurant, Florence; Miramand, Pierre

    2002-01-01

    International audience The high concentrations of cadmium recorded in the digestive gland of cephalopods from various temperate and subpolar waters suggest that these molluscs have developed efficient cadmium detoxification mechanisms. The subcellular distribution of cadmium in the digestive gland cells was investigated in seven cephalopod species from the Bay of Biscay (France) and the Faroe Islands. In most species, cadmium was mainly found in the cytosolic fraction of the digestive glan...

  10. Cadmium content of plants as affected by soil cadmium concentration

    Energy Technology Data Exchange (ETDEWEB)

    Lehoczky, E. [Pannon Univ. of Agricultural Sciences, Keszthely (Hungary); Szabados, I.; Marth, P. [Plant Health and Soil Conservation Station, Higany (Hungary)

    1996-12-31

    Pot experiments were conducted in greenhouse conditions to study the effects of increasing cadmium (Cd) levels on biomass production and Cd contents in corn, (Zea mays L.), garlic (Allium sativum L.), and spinach (Spinacia oleracea L.). Plants were grown in two soil types: Eutric cambisol soil and A gleyic luvisol soil. Spinach proved to be the most sensitive to Cd treatments as its biomass considerably decreased with the increasing Cd levels. Cadmium contents of the three crops increased with increasing levels of Cd applications. Statistical differences were observed in the Cd contents of crops depending on soil type. With the same Cd rates, Cd tissue concentration of test plants grown in the strongly acidic Gleyic luvisol soil were many times higher than that of plants grown in a neutral Eutric cambisol soil. 14 refs., 4 tabs.

  11. Cadmium Exposure and Pancreatic Cancer in South Louisiana

    OpenAIRE

    Luckett, Brian G.; L. Joseph Su; Rood, Jennifer C.; Elizabeth T. H. Fontham

    2012-01-01

    Cadmium has been hypothesized to be a pancreatic carcinogen. We test the hypothesis that cadmium exposure is a risk factor for pancreatic cancer with a population-based case-control study sampled from a population with persistently high rates of pancreatic cancer (south Louisiana). We tested potential dietary and nondietary sources of cadmium for their association with urinary cadmium concentrations which reflect long-term exposure to cadmium due to the accumulation of cadmium in the kidney c...

  12. Influence of the orientation of methylammonium lead iodide perovskite crystals on solar cell performance

    OpenAIRE

    Pablo Docampo; Hanusch, Fabian C.; Nadja Giesbrecht; Philipp Angloher; Alesja Ivanova; Thomas Bein

    2014-01-01

    Perovskite solar cells are emerging as serious candidates for thin film photovoltaics with power conversion efficiencies already exceeding 16%. Devices based on a planar heterojunction architecture, where the MAPbI3 perovskite film is simply sandwiched between two charge selective extraction contacts, can be processed at low temperatures (

  13. Zone refining of cadmium and related characterization

    Indian Academy of Sciences (India)

    N R Munirathnam; D S Prasad; Ch Sudheer; J V Rao; T L Prakash

    2005-06-01

    We present the zone refining results of cadmium using horizontal resistive zone refiner under constant flow of moisture free hydrogen gas. The boron impurity in cadmium can be avoided using quartz (GE 214 grade) boat in lieu of high pure graphite boat. The analytical results using inductively coupled plasma optical emission spectrometry (ICPOES) show that majority of the impurities are less than the detection limits. Comparatively, zinc is the most difficult impurity element to remove in cadmium matrix by zone refining.

  14. Electrodialytic Removal of Cadmium from Straw Ash

    DEFF Research Database (Denmark)

    Hansen, Henrik; Ottosen, Lisbeth M.; Villumsen, Arne;

    1999-01-01

    A problem with flyash from straw and wood combustion is the high level of heavy metals, especially cadmium. Two electrodialytic remediation experiments were carried out on cadmium polluted flyash from straw combustion. The flyash could be cleaned to 1/3 of its initial level after 24 days...... of remediation. Further removal of cadmium could be possible with longer remediation time or a higher current density...

  15. Experimental and theoretical studies of the second- and third-order NLO properties of a semi-organic compound: 6-Aminoquinolinium iodide monohydrate

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Pedro S. Pereira, E-mail: psidonio@pollux.fis.uc.pt [CEMDRX, Physics Department, University of Coimbra, P-3004-516 Coimbra (Portugal); El Ouazzani, Hasnaa; Pranaitis, Mindaugas [Institut des Sciences et Technologies Moléculaires d’Angers, MOLTECH ANJOU, CNRS UMR 6200, Université d’Angers, 2 Bd Lavoisier, 49045 Angers Cedex (France); Silva, Manuela Ramos [CEMDRX, Physics Department, University of Coimbra, P-3004-516 Coimbra (Portugal); Arranja, Cláudia T.; Sobral, Abilio J.F.N. [Department of Chemistry, University of Coimbra, P-3004-516 Coimbra (Portugal); Sahraoui, Bouchta [Institut des Sciences et Technologies Moléculaires d’Angers, MOLTECH ANJOU, CNRS UMR 6200, Université d’Angers, 2 Bd Lavoisier, 49045 Angers Cedex (France); Paixão, José A. [CEMDRX, Physics Department, University of Coimbra, P-3004-516 Coimbra (Portugal)

    2014-01-15

    Highlights: • Synthesis and structure of 6-aminoquinolinium iodide monohydrate is reported. • UV–vis absorption and fluorescence spectra are reported. • SHG and THG signals measured with the Maker fringes technique. • Hyperpolarizabilities calculated with the DFT and MP2 methods. • Behaviour of hybrid functionals corrected with ESP charges. - Abstract: A new semi-organic compound, 6-aminoquinolinium iodide monohydrate (I), has been synthesized and characterized by single crystal X-ray diffraction, UV–vis absorption and fluorescence spectroscopy and nonlinear optical (NLO) measurements. The second- and third-order NLO responses were investigated with the second- and third-harmonic Maker fringes techniques, carried out on thin films at a fundamental wavelength of 1064 nm. From the molecular structure, the molecular hyperpolarizability tensors were determined with density functional theory and second-order Møller–Plesset perturbation method. The second- and third-order susceptibility tensors of the reported crystal were evaluated using the oriented gas model with the Lorenz–Lorentz and the Wortmann–Bishop local-field corrections. The calculations using the Wortmann–Bishop local-field were able to reproduce the correct order of magnitude of the experimental third-order susceptibilities. The value of χ{sup (3)} obtained by summing the effective third-order polarizability calculated for the asymmetric unit surrounded by ESP-derived charges have also the same order of magnitude of the experimental.

  16. Removal efficiency of radioactive methyl iodide on TEDA-impregnated activated carbons

    Energy Technology Data Exchange (ETDEWEB)

    Gonzalez-Garcia, C.M.; Gonzalez, J.F.; Roman, S. [Extremadura Univ., Badajoz (Spain). Dept. de Fisica Aplicada

    2011-02-15

    Activated carbons were prepared by different series of carbon dioxide and steam activation from walnut shells for their optimal use as radioactive methyl iodide adsorbents in Nuclear Plants. The knowledge of the most favourable textural characteristics of the activated carbons was possible by the previous study of the commercial activated carbon currently used for this purpose. In order to increase their methyl iodide affinity, the effect of triethylenediamine impregnation was studied at 5 and 10 wt.%. The results obtained indicated that in both cases the adsorption efficiency is markedly improved by the addition of impregnant, which allows the adsorbate uptake to occur not only by physical adsorption, via non-specific interactions (as in non-impregnated carbons) but also by the specific interaction of triethylenediamine with radioactive methyl iodide. Methyl iodide retention efficiencies up to 98.1% were achieved. (author)

  17. Kinetics and mechanism of the mercury(II)-assisted hydrolysis of methyl iodide.

    Science.gov (United States)

    Celo, Valbona; Scott, Susannah L

    2005-04-01

    The kinetics and mechanism of the reaction of aqueous Hg(II) with methyl iodide have been investigated. The overall reaction is best described as Hg(II)-assisted hydrolysis, resulting in quantitative formation of methanol and, in the presence of excess methyl iodide, ultimately, HgI2 via the intermediate HgI+. The kinetics are biexponential when methyl iodide is in excess. At 25 degrees C, the acceleration provided by Hg2+ is 7.5 times greater than that caused by HgI+, while assistance of hydrolysis was not observed for HgI2. Thus, the reactions are not catalytic in Hg(II). The kinetics are consistent with an SN2-M+ mechanism involving electrophilic attack at iodide. As expected, methylation of mercury is not a reaction pathway; traces of methylmercury(II) are artifacts of the extraction/preconcentration procedure used for methylmercury analysis.

  18. Fluorescence characteristics of 5-amino salicylic acid: An iodide recognition study

    Science.gov (United States)

    Arora, Priyanka; Suyal, Kanchan; Joshi, Neeraj K.; Joshi, Hem Chandra; Pant, Sanjay

    In this paper we report the effect of iodide on the fluorescence of 5-amino salicylic acid (5-ASA). In the absence of iodide, prominent blue green (BG) emission band at ˜465 nm (broad) is observed in aprotic solvents whereas violet (V) emission at ˜408 nm, blue green (BG) at ˜480 nm and green (G) at ˜500 nm are observed in case of protic solvents. On the addition of iodide ion (I-), the intensity of BG fluorescence is enhanced in case of aprotic solvents. On the other hand the G band is enhanced in protic solvents and decrease in the intensity of the V band is observed. The effect of hydrogen bonding as well as the interplay of neutral and ionic species is invoked to explain the observed results. The study projects the application of this system in iodide recognition in protic/aprotic environments.

  19. A Direct Transformation of Aryl Aldehydes to Benzyl Iodides Via Reductive Iodination

    Energy Technology Data Exchange (ETDEWEB)

    Ruso, Jayaraman Sembian; Rajendiran, Nagappan; Kumaran, Rajendran Senthil [Univ. of Madras, Chennai (India)

    2014-02-15

    A facile transformation of aryl aldehydes to benzyl iodides through one-pot reductive iodination is reported. This protocol displays remarkable functional group tolerance and the title compound was obtained in good to excellent yield.

  20. Bioavailability of cadmium from linseed and cocoa

    OpenAIRE

    Hansen, Max; Rasmussen, Rie Romme; Sloth, Jens Jørgen

    2014-01-01

    The exposure of the European population to cadmium from food is high compared with the tolerable weekly intake of 2.5 μg/kg bodyweight set by EFSA in 2009. Only few studies on the bioavailability of cadmium from different food sources has been performed but this information in very important for the food authorities in order to give correct advises to the population. The aim of this study was to investigate the bioavailability of cadmium from whole linseed, crushed linseed, cocoa and cadmium ...

  1. The Epigenetic Effects of Prenatal Cadmium Exposure.

    Science.gov (United States)

    Vilahur, Nadia; Vahter, Marie; Broberg, Karin

    2015-06-01

    Prenatal exposure to the highly toxic and common pollutant cadmium has been associated with adverse effects on child health and development. However, the underlying biological mechanisms of cadmium toxicity remain partially unsolved. Epigenetic disruption due to early cadmium exposure has gained attention as a plausible mode of action, since epigenetic signatures respond to environmental stimuli and the fetus undergoes drastic epigenomic rearrangements during embryogenesis. In the current review, we provide a critical examination of the literature addressing prenatal cadmium exposure and epigenetic effects in human, animal, and in vitro studies. We conducted a PubMed search and obtained eight recent studies addressing this topic, focusing almost exclusively on DNA methylation. These studies provide evidence that cadmium alters epigenetic signatures in the DNA of the placenta and of the newborns, and some studies indicated marked sexual differences for cadmium-related DNA methylation changes. Associations between early cadmium exposure and DNA methylation might reflect interference with de novo DNA methyltransferases. More studies, especially those including environmentally relevant doses, are needed to confirm the toxicoepigenomic effects of prenatal cadmium exposure and how that relates to the observed health effects of cadmium in childhood and later life.

  2. Horseradish Peroxidase-Mediated, Iodide-Catalyzed Cascade Reaction for Plasmonic Immunoassays.

    Science.gov (United States)

    Xianyu, Yunlei; Chen, Yiping; Jiang, Xingyu

    2015-11-01

    This report outlines an enzymatic cascade reaction for signal transduction and amplification for plasmonic immunoassays by using horseradish peroxidase (HRP)-mediated aggregation of gold nanoparticles (AuNPs). HRP-catalyzed oxidation of iodide and iodide-catalyzed oxidation of cysteine is employed to modulate the plasmonic signals of AuNPs. It agrees well with the current immunoassay platforms and allows naked-eye readout with enhanced sensitivity, which holds great promise for applications in resource-constrained settings.

  3. Synthesis, crystal structure and luminescence of a one-dimensional cadmium ( Ⅱ ) coordination polymer%一维链状Cd(Ⅱ)配位聚合物的合成、晶体结构及荧光性质

    Institute of Scientific and Technical Information of China (English)

    刘海燕; 孙红梅; 乔秀丽; 迟云超; 王广慧

    2011-01-01

    由Cd(CH3COO)2、间苯二甲酸(H2L)和柔性含氮配体2,2′-二[2-(2-吡啶)苯并咪唑]乙醚(bpb)反应,得了一种新型配合物[Cd2( L)2 (bpb)],通过元素分析、红外光谱和X-单晶衍射等对配合物的结构进行了表征.结果表明配合物属单斜晶系,空间群P2/c,晶胞参数a=0.931 8(5),b=1.076 7(5),c=1.9004(5) nm,β=96.258(5)°,V= 1.895 3(14) nm3,Z=2,F(000)=1 012,Dc=1.776 g/cm3,R1 =0.045 0,wR2= 0.080 5[I> 2σ(Ⅰ)].配合物中Cd离子被L2-阴离子连接成一维的链状结构,中性bpb配体建立一个“U”型的构型,依次配位于链的两侧.最终这些链通过π…π的相互作用形成三维超分子结构.此外,还研究了该化合物在室温下的固体荧光性质.%A new complex [Cd2(L)2(bpb)] was synthesized using m-benzenedicarboxylate acid (H2L) ,2,2'-bis[2-(2-pyridyl)benzimidazole]ether (bpb),and Cd(CH3COO)2.Its structure has been determined by single crystal Xray diffraction analysis and further characterized by elemental analysis and IR spectrum. This complex belongs to monochrac system,space group P2/c with a =0.931 8(5), 6 = 1.076 7(5),c = 1.900 4(5) nm,β = 96.258 (5)°, V= 11.895 3(14) nm3,Z = 2,F(000) = 1012,Dc = 1.776g/cm3,R1=0.045 0,wR2 = 0.080 5 [I>2σ ( Ⅰ )] .In complex,the Cd (Ⅱ) cations are linked by the L2-r anions to form a ones-dimensional chain structure. The bpb ligand exhibits a "U-shaped" conformation,attaching to both sides of the chain. Finally, the chains are extended into a three-dimensional supramolecular structure through n-iz interactions. In addition,the luminescent property of complex is also discussed in the solid state at room temperature.

  4. Polarization Effects in Methylammonium Lead Iodide Electronic Devices

    Science.gov (United States)

    Labram, John; Fabini, Douglas; Perry, Erin; Lehner, Anna; Wang, Hengbin; Glaudell, Anne; Wu, Guang; Evans, Hayden; Buck, David; Cotta, Robert; Echegoyen, Luis; Wudl, Fred; Seshadri, Ram; Chabinyc, Michael

    The immense success of group IV and III-V semiconductors has resulted in disruptive new photovoltaic (PV) cell technologies emerging extremely infrequently. For this reason, the recent progress in Methylammonium Lead Iodide (MAPbI3) solar cells can be viewed as a highly significant historic event. Despite the staggering recent progress made in reported power conversion efficiency (PCE), debate remains intense on the nature of the various instabilities synonymous with these devices. Using various electronic device measurements, we here present a body of experimental evidence consistent with the existence of a mobile ionic species within the MAPbI3 perovskite. Temperature-dependent transistor measurements reveal operating FET devices only below approximately 210K. This is attributed to ionic screening of the (otherwise charge-neutral) semiconductor-dielectric interface. Temperature-dependent pulsed-gate and impedance spectroscopy experiments also reveal behavior consistent with this interpretation. MAPbI3 PV cells were found to possess a PCE which decreases significantly below 210K. Combined, these set of measurements provide an interesting and consistent description of the internal processes at play within the MAPbI3 perovskite structure.

  5. Thermopower and activation energy of silver iodide based superionic materials

    International Nuclear Information System (INIS)

    Silver iodide based glasses, 60Agl-20Ag sub 2 O-20B sub 2O sub 3, 6 Agl-20Ag sub 2 O-20 MoO sub 3 and 60Agl-20Ag sub 2O-20WO sub 3, all in the mol % ratio, were prepared by rapidly quenching the melts of the chemicals in a stainless steel container; kept in a liquid nitrogen bath. The glassy nature of the as-quenched materials was confirmed by X-ray diffraction (XRD). The electrical conductivity of the glasses was measured at various temperatures ranging from 30 to 70 degree C using an impedance bridge operating in the frequency range between 40 Hz to 100 kHz. The plot of In σT versus 1000/T for each glassy material obeys Arrhenius law and the activation energy obtained is between 0.2 to 0.3 eV. Thermopower measurement was also carried out in the same temperature range as the conductivity measurement to obtain the heat of transport

  6. Persistent photovoltage in methylammonium lead iodide perovskite solar cells

    Directory of Open Access Journals (Sweden)

    A. Baumann

    2014-08-01

    Full Text Available We herein perform open circuit voltage decay (OCVD measurements on methylammonium lead iodide (CH3NH3PbI3 perovskite solar cells to increase the understanding of the charge carrier recombination dynamics in this emerging technology. Optically pulsed OCVD measurements are conducted on CH3NH3PbI3 solar cells and compared to results from another type of thin-film photovoltaics, namely, the two reference polymer–fullerene bulk heterojunction solar cell devices based on P3HT:PC60BM and PTB7:PC70BM blends. We observe two very different time domains of the voltage transient in the perovskite solar cell with a first drop on a short time scale that is similar to the decay in the studied organic solar cells. However, 65%–70% of the maximum photovoltage persists on much longer timescales in the perovskite solar cell than in the organic devices. In addition, we find that the recombination dynamics in all time regimes are dependent on the starting illumination intensity, which is also not observed in the organic devices. We then discuss the potential origins of these unique behaviors.

  7. Critical Evaluation of Acetylthiocholine Iodide and Acetylthiocholine Chloride as Substrates for Amperometric Biosensors Based on Acetylcholinesterase

    Directory of Open Access Journals (Sweden)

    Gabriel-Lucian Radu

    2013-01-01

    Full Text Available Numerous amperometric biosensors have been developed for the fast analysis of neurotoxic insecticides based on inhibition of cholinesterase (AChE. The analytical signal is quantified by the oxidation of the thiocholine that is produced enzymatically by the hydrolysis of the acetylthiocholine pseudosubstrate. The pseudosubstrate is a cation and it is associated with chloride or iodide as corresponding anion to form a salt. The iodide salt is cheaper, but it is electrochemically active and consequently more difficult to use in electrochemical analytical devices. We investigate the possibility of using acetylthiocholine iodide as pseudosubstrate for amperometric detection. Our investigation demonstrates that operational conditions for any amperometric biosensor that use acetylthiocholine iodide must be thoroughly optimized to avoid false analytical signals or a reduced sensitivity. The working overpotential determined for different screen-printed electrodes was: carbon-nanotubes (360 mV, platinum (560 mV, gold (370 mV, based on a catalytic effect of iodide or cobalt phthalocyanine (110 mV, but with a significant reduced sensitivity in the presence of iodide anions.

  8. Experimental study of retinoic acid on improving iodide uptake in MCF-7 breast cancer cells

    Institute of Scientific and Technical Information of China (English)

    FU Hong-Liang; WU Jing-Chuan; DU Xue-Liang; LI Jia-Ning; WU Zhen; ZOU Ren-Jian

    2005-01-01

    The study aims to investigate the effect of retinoic acid on the iodide uptake of MCF-7 cells and its mechanism. The iodide uptake and expression of hNIS(human sodium/iodide symporter)mRNA in the breast cancer MCF-7 cells were compared individually before and after the intervention of all-trans retinoic acid (ATRA) with the iodide uptake assay and RT-PCR. The following results are obtained: (1) when treated with all-trans retinoic acid in the concentration of 1.0 μmol/L, the capacity of iodide uptake of MCF-7 cells reached about 1.5 times of the basal state; (2) 12 h after the intervention of 1.0 μmol/L ATRA, the hNISmRNA expression of the MCF-7 cells reached maximum. The study shows that all-trans retinoic acid has the effect to improve the iodide uptake of the MCF-7 cells and this effect may result from its up-regulation of the hNISmRNA expression.

  9. Modelling iodide – iodate speciation in atmospheric aerosol: Contributions of inorganic and organic iodine chemistry

    Directory of Open Access Journals (Sweden)

    S. Pechtl

    2007-01-01

    Full Text Available The speciation of iodine in atmospheric aerosol is currently poorly understood. Models predict negligible iodide concentrations but accumulation of iodate in aerosol, both of which is not confirmed by recent measurements. We present an updated aqueous phase iodine chemistry scheme for use in atmospheric chemistry models and discuss sensitivity studies with the marine boundary layer model MISTRA. These studies show that iodate can be reduced in acidic aerosol by inorganic reactions, i.e., iodate does not necessarily accumulate in particles. Furthermore, the transformation of particulate iodide to volatile iodine species likely has been overestimated in previous model studies due to negligence of collision-induced upper limits for the reaction rates. However, inorganic reaction cycles still do not seem to be sufficient to reproduce the observed range of iodide – iodate speciation in atmospheric aerosol. Therefore, we also investigate the effects of the recently suggested reaction of HOI with dissolved organic matter to produce iodide. If this reaction is fast enough to compete with the inorganic mechanism, it would not only directly lead to enhanced iodide concentrations but, indirectly via speed-up of the inorganic iodate reduction cycles, also to a decrease in iodate concentrations. Hence, according to our model studies, organic iodine chemistry, combined with inorganic reaction cycles, is able to reproduce observations. The presented chemistry cycles are highly dependent on pH and thus offer an explanation for the large observed variability of the iodide – iodate speciation in atmospheric aerosol.

  10. A selective iodide ion sensor electrode based on functionalized ZnO nanotubes.

    Science.gov (United States)

    Ibupoto, Zafar Hussain; Khun, Kimleang; Willander, Magnus

    2013-01-01

    In this research work, ZnO nanotubes were fabricated on a gold coated glass substrate through chemical etching by the aqueous chemical growth method. For the first time a nanostructure-based iodide ion selective electrode was developed. The ZnO nanotubes were functionalized with miconazole ion exchanger and the electromotive force (EMF) was measured by the potentiometric method. The iodide ion sensor exhibited a linear response over a wide range of concentrations (1 × 10-6 to 1 × 10-1 M) and excellent sensitivity of -62 ± 1 mV/decade. The detection limit of the proposed sensor was found to be 5 × 10-7 M. The effects of pH, temperature, additive, plasticizer and stabilizer on the potential response of iodide ion selective electrode were also studied. The proposed iodide ion sensor demonstrated a fast response time of less than 5 s and high selectivity against common organic and the inorganic anions. All the obtained results revealed that the iodide ion sensor based on functionalized ZnO nanotubes may be used for the detection of iodide ion in environmental water samples, pharmaceutical products and other real samples. PMID:23385412

  11. A Selective Iodide Ion Sensor Electrode Based on Functionalized ZnO Nanotubes

    Directory of Open Access Journals (Sweden)

    Magnus Willander

    2013-02-01

    Full Text Available In this research work, ZnO nanotubes were fabricated on a gold coated glass substrate through chemical etching by the aqueous chemical growth method. For the first time a nanostructure-based iodide ion selective electrode was developed. The ZnO nanotubes were functionalized with miconazole ion exchanger and the electromotive force (EMF was measured by the potentiometric method. The iodide ion sensor exhibited a linear response over a wide range of concentrations (1 × 10−6 to 1 × 10−1 M and excellent sensitivity of –62 ± 1 mV/decade. The detection limit of the proposed sensor was found to be 5 × 10−7 M. The effects of pH, temperature, additive, plasticizer and stabilizer on the potential response of iodide ion selective electrode were also studied. The proposed iodide ion sensor demonstrated a fast response time of less than 5 s and high selectivity against common organic and the inorganic anions. All the obtained results revealed that the iodide ion sensor based on functionalized ZnO nanotubes may be used for the detection of iodide ion in environmental water samples, pharmaceutical products and other real samples.

  12. Silver-cadmium alloys: Physical and metallurgical properties. (Latest citations from the EI Compendex*plus database). Published Search

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1996-05-01

    The bibliography contains citations concerning the metallurgical and physical properties of silver-cadmium alloys, oxides, and sulfides. The phase relationships and crystal structure of this alloy system are presented. Applications for electrical contact devices are discussed extensively. (Contains 50-250 citations and includes a subject term index and title list.) (Copyright NERAC, Inc. 1995)

  13. Growth and characterization of potassium strontium iodide: A new high light yield scintillator with 2.4% energy resolution

    Energy Technology Data Exchange (ETDEWEB)

    Stand, L., E-mail: lstand@utk.edu [Scintillation Materials Research Center, University of Tennessee, Knoxville, TN (United States); Materials Science and Engineering, University of Tennessee, Knoxville, TN (United States); Zhuravleva, M.; Lindsey, A. [Scintillation Materials Research Center, University of Tennessee, Knoxville, TN (United States); Materials Science and Engineering, University of Tennessee, Knoxville, TN (United States); Melcher, C.L. [Scintillation Materials Research Center, University of Tennessee, Knoxville, TN (United States)

    2015-04-21

    A new ternary metal halide scintillator, potassium strontium iodide, activated with divalent europium (KSr{sub 2}I{sub 5}:Eu) has been discovered. This material has a monoclinic crystal structure with a density of 4.39 g/cm{sup 3}. Differential scanning calorimetry indicates a congruent melting point of 470 °C and suggests that this compound has no solid–solid phase transitions. As is the case with most metal halides, the material is hygroscopic, and it has some internal radioactivity due to the presence of {sup 40}K. Single crystals of KSr{sub 2}I{sub 5} doped with 4% Eu{sup 2+} were grown in evacuated quartz ampoules via the Bridgman technique. The X-ray excited emission spectrum consisted of a single peak at ~445 nm due to the 5d–4f transition in Eu{sup 2+}. The measured light yield is ~94,000 photons/MeV with an energy resolution of 2.4% at 662 keV. The crystal has an excellent proportionality response over a wide range of energies from 14 keV to 1275 keV. - Highlights: • New Eu{sup 2+}-doped scintillators KSr{sub 2}I{sub 5}. • Single crystals of KSr{sub 2}I{sub 5}:Eu 4% were grown using the Bridgman technique. • This new material exhibit excellent properties for X-ray and gamma-ray detections. • Light yield of 94,000 ph/MeV and energy resolution of 2.4% at 662 keV.

  14. Synthesis, Crystal Structure and Photoluminescence of a 2D Cadmium(Ⅱ) Complex, [Cd(mpac)(4, 4-bpy)(OH)]n%二维配合物[Cd(mpac)(4,4-bpy)(OH)]n的合成,晶体结构和荧光性质

    Institute of Scientific and Technical Information of China (English)

    林培喜; 康新平; 安哲

    2011-01-01

    溶剂热条件下采用Cd(NO3)2· 4H2O,5-甲基吡嗪-2-甲酸和4,4-联吡啶作为反应物合成出一个新的具有二维层状结构的镉金属配位聚合物[Cd(mpac)(4,4-bpy)(OH)]n(1),并分别用元素分析,红外光谱,热重分析和x-射线单晶衍射表征该结构.晶体结构分析结果表明:5-甲基吡嗪-2-甲酸将cd(Ⅱ)离子连接成一维链,这些链进一步被4,4-联吡啶连接成二维层状结构.在二维层状结构中存在大小为0.24×1.16nm2的一维通道.荧光谱图表明常温固态下配合物1发射蓝色荧光.%A 2D cadmium coordination polymer,[Cd (mpac)(4,4-bpy)(OH)]n (1) (Hmpac =5-methy1-2-pyrazinecarboxylic acid,4,4-bpy=4,4-bipyridine) has been synthesized by solvothermal method and characterized by elemental analysis,IR,TGA and single-crystal X-ray diffraction.The mpac ligands link the Cd(Ⅱ) atoms to form an infinite Cd-carboxylate chain.These chains are further bridged by 4,4-bpy ligands,forming a new twodimensional layered network.Interestingly,there are small channels of 0.24x1.16 nm2 within the 2D individual layers along the b-axis.Furthermore,the luminescent property of complex 1 was investigated at room temperature.CCDC:808271.

  15. Improvement of cadmium phytoremediation after soil inoculation with a cadmium-resistant Micrococcus sp.

    Science.gov (United States)

    Sangthong, Chirawee; Setkit, Kunchaya; Prapagdee, Benjaphorn

    2016-01-01

    Cadmium-resistant Micrococcus sp. TISTR2221, a plant growth-promoting bacterium, has stimulatory effects on the root lengths of Zea mays L. seedlings under toxic cadmium conditions compared to uninoculated seedlings. The performance of Micrococcus sp. TISTR2221 on promoting growth and cadmium accumulation in Z. mays L. was investigated in a pot experiment. The results indicated that Micrococcus sp. TISTR2221significantly promoted the root length, shoot length, and dry biomass of Z. mays L. transplanted in both uncontaminated and cadmium-contaminated soils. Micrococcus sp. TISTR2221 significantly increased cadmium accumulation in the roots and shoots of Z. mays L. compared to uninoculated plants. At the beginning of the planting period, cadmium accumulated mainly in the shoots. With a prolonged duration of cultivation, cadmium content increased in the roots. As expected, little cadmium was found in maize grains. Soil cadmium was significantly reduced with time, and the highest percentage of cadmium removal was found in the bacterial-inoculated Z. mays L. after transplantation for 6 weeks. We conclude that Micrococcus sp. TISTR2221 is a potent bioaugmenting agent, facilitating cadmium phytoextraction in Z. mays L.

  16. Solid state structures of cadmium complexes with relevance for biological systems.

    Science.gov (United States)

    Carballo, Rosa; Castiñeiras, Alfonso; Domínguez-Martín, Alicia; García-Santos, Isabel; Niclós-Gutiérrez, Juan

    2013-01-01

    This chapter provides a review of the literature on structural information from crystal structures determined by X-ray diffractometry of cadmium(II) complexes containing ligands of potential biological interest. These ligands fall into three broad classes, (i) those containing N-donors such as purine or pyrimidine bases and derivatives of adenine, guanine or cytosine, (ii) those containing carboxylate groups such as α-amino acids, in particular the twenty essential ones, the water soluble vitamins (B-complex) or the polycarboxylates of EDTA type ligands, and (iii) S-donors such as thiols/thiolates or dithiocarbamates. A crystal and molecular structural analysis has been carried out for some representative complexes of these ligands, specifically addressing the coordination mode of ligands, the coordination environment of cadmium and, in some significant cases, the intermolecular interactions. PMID:23430774

  17. A glucose bio-battery prototype based on a GDH/poly(methylene blue) bioanode and a graphite cathode with an iodide/tri-iodide redox couple.

    Science.gov (United States)

    Wang, Jen-Yuan; Nien, Po-Chin; Chen, Chien-Hsiao; Chen, Lin-Chi; Ho, Kuo-Chuan

    2012-07-01

    A glucose bio-battery prototype independent of oxygen is proposed based on a glucose dehydrogenase (GDH) bioanode and a graphite cathode with an iodide/tri-iodide redox couple. At the bioanode, a NADH electrocatalyst, poly(methylene blue) (PMB), which can be easily grown on the electrode (screen-printed carbon paste electrode, SPCE) by electrodeposition, is harnessed and engineered. We find that carboxylated multi-walled carbon nanotubes (MWCNTs) are capable of significantly increasing the deposition amount of PMB and thus enhancing the PMB's electrocatalysis of NADH oxidation and the glucose bio-battery's performance. The choice of the iodide/tri-iodide redox couple eliminates the dependence of oxygen for this bio-battery, thus enabling the bio-battery with a constant current-output feature similar to that of the solar cells. The present glucose bio-battery prototype can attain a maximum power density of 2.4 μW/cm(2) at 25 °C. PMID:22541949

  18. Cadmium Modulates Biofilm Formation by Staphylococcus epidermidis

    NARCIS (Netherlands)

    Wu, Xueqing; Santos, Regiane R.; Fink-Gremmels, Johanna

    2015-01-01

    The aim of the study was to evaluate the effect of cadmium exposure on Staphylococcus epidermidis (ATCC 35984) biofilm formation. Bacteria were cultured in the absence or presence of different concentrations (0-50 mu M) of cadmium. Biofilm formation and bacterial viability were assessed. Quantitativ

  19. Characterization of strontium iodide scintillators with silicon photomultipliers

    Science.gov (United States)

    Mitchell, Lee J.; Phlips, Bernard

    2016-06-01

    This work characterizes a commercially available europium-doped strontium iodide detector recently developed by Radiation Monitoring Devices (RMD). The detector has been chosen for a space-based mission scheduled to launch in early 2017. The primary goal of this work was to characterize the detector's response over the expected operational range of -10 °C to 30 °C as well as the expected operational voltage range of +26.5-+28.5 V and identify background interferences that may develop due to neutron activation produced by cosmic-ray interactions. The 8 mm×8 mm×20 mm detectors use KETEK silicon photomultipliers (SiPM), with an active area of 6 mmx6 mm (KETEK PM6660). Our results show substantial integral nonlinearity due to the SiPM ranging from 0% to 25% at room temperature over the energy range of 80-2614 keV. The nonlinearity, a function of temperature and overvoltage, leads to an underestimate of the full width at half max (FWHM), which is 2.6% uncorrected at 662 keV and 3.8% corrected at 662 keV. The temperature dependence of the detector results in a noise threshold that increases substantially above 30 °C due to the SiPM dark rate. In an effort to simulate the harsh environment of space, neutron activation of the detector was also explored. Gamma-ray lines at 127 keV and 164 keV were observed in the detector along with Kα x-rays associated with europium. Beta decay from europium- and iodine-activation products were also observed within the detector.

  20. THERAPY OF GRAVES’ DISEASE WITH SODIUM IODIDE-131

    Directory of Open Access Journals (Sweden)

    I Wayan Hartadi Noor

    2013-11-01

    Full Text Available Normal 0 false false false EN-US X-NONE X-NONE MicrosoftInternetExplorer4 Graves’ disease is the most common form of thyrotoxicosis, with a peak incidence in the 20-40 year of age group. Females are involved about five times more commonly than male. The easiest sign to recognize patients with Graves’ disease is the present of Graves’ ophthalmopathy. The diagnosis of Graves’ disease may sometimes base only on a physical examination and a medical history. Diffuse thyroid enlargement and sign of thyrotoxicosis, mainly ophthalmopathy and to lesser extent dermopathy, usually adequate for diagnosis. TSH test combined with FT4 test is usually the first laboratory test performs in these patients. The patients suffered Graves’ disease can be treated with antithyroid drug therapy or undergo subtotal Thyroidectomy. Another therapy is by using sodium iodide-131, where this therapy has advantages including easy administration, effectiveness, low expense, and absence of pain. /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-qformat:yes; mso-style-parent:""; mso-padding-alt:0in 5.4pt 0in 5.4pt; mso-para-margin:0in; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:"Times New Roman"; mso-fareast-theme-font:minor-fareast; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-bidi-font-family:"Times New Roman"; mso-bidi-theme-font:minor-bidi;}

  1. Imaging with polycrystalline mercuric iodide detectors using VLSI readout

    Energy Technology Data Exchange (ETDEWEB)

    Turchetta, R.; Dulinski, W.; Husson, D.; Riester, J.L.; Schieber, M.; Zuck, A.; Melekhov, L.; Saado, Y.; Hermon, H.; Nissenbaum, J

    1999-06-01

    Potentially low cost and large area polycrystalline mercuric iodide room-temperature radiation detectors, with thickness of 100-600 {mu}m have been successfully tested with dedicated low-noise, low-power mixed signal VLSI electronics which can be used for compact, imaging solutions. The detectors are fabricated by depositing HgI{sub 2} directly on an insulating substrate having electrodes in the form of microstrips and pixels with an upper continuous electrode. The deposition is made either by direct evaporation or by screen printing HgI{sub 2} mixed with glue such as Poly-Vinyl-Butiral. The properties of these first-generation detectors are quite uniform from one detector to another. Also for each single detector the response is quite uniform and no charge loss in the inter-electrode space have been detected. Because of the low cost and of the polycrystallinity, detectors can be potentially fabricated in any size and shape, using standard ceramic technology equipment, which is an attractive feature where low cost and large area applications are needed. The detectors which act as radiation counters have been tested with a beta source as well as in a high-energy beam of 100 GeV muons at CERN, connected to VLSI, low noise electronics. Charge collection efficiency and uniformity have been studied. The charge is efficiently collected even in the space between strips indicating that fill factors of 100% could be reached in imaging applications with direct detection of radiation. Single photon counting capability is reached with VLSI electronics. These results show the potential of this material for applications demanding position sensitive, radiation resistant, room-temperature operating radiation detectors, where position resolution is essential, as it can be found in some applications in high-energy physics, nuclear medicine and astrophysics.

  2. Cadmium stress in wheat seedlings: growth, cadmium accumulation and photosynthesis

    DEFF Research Database (Denmark)

    Ci, Dunwei; Jiang, Dong; Wollenweber, Bernd;

    2010-01-01

    Seedlings of wheat (Triticum aestivum L.) cultivars Jing 411, Jinmai 30 and Yangmai 10 were exposed to 0, 10, 20, 30, 40 or 50 μM of CdCl2 in a solution culture experiment. The effects of cadmium (Cd) stress on wheat growth, leaf photon energy conversion, gas exchange, and Cd accumulation in wheat...... parameters were generally depressed by Cd stress, especially under the high Cd concentrations. Cd concentration and accumulation in both shoots and roots increased with increasing external Cd concentrations. Relationships between corrected parameters of growth, photosynthesis and fluorescence and corrected...

  3. Immunoassay for Cadmium Detection and Quantification

    Institute of Scientific and Technical Information of China (English)

    GONG-LIANG LIU; JU-FANG WANG; ZHI-YONG LI; SHI-ZHONG LIANG; XIAO-NING WANG

    2009-01-01

    Objective To detect cadmium in environmental and food samples by graphite furnace atomic absorption spectroscopy (GFAAS) and inductively coupled plasma atomic emission spectroscopy (ICPAES). Methods An indirect competitive enzyme-linked immunosorbent assay (IC-ELISA) was developed based on a cadmium-specific monoclonal antibody.IC-ELISA for cadmium in environmental and food samples was evaluated. Results IC-ELISA showed an IC50 of 45.6 μg/L with a detection limit of 1.95 μg/L for cadmium,and showed a mean recovery ranging 97.67%-107.08%.The coefficient of variations for intra- and iuterassay was 3.41%-6.61% and 4.70%-9.21%,respectively.The correlation coefficient between IC-ELISA and GFAAS was 0.998. Conclusion IC-ELISA can detect and quantify cadmium residue in environmental or food samples.

  4. Cadmium mobility and accumulation in soils of the European Communities

    NARCIS (Netherlands)

    Fraters B; van Beurden AUCJ

    1993-01-01

    In this overview of the effects of cadmium pollution on agricultural soils in the European Community, both the cadmium loads on agricultural land and the soil sensitivity to cadmium accumulation have been estimated. Cadmium loads have been estimated separately for arable land and grassland. The ef

  5. Peculiarities of preparation of cadmium isotopes of high enrichment

    International Nuclear Information System (INIS)

    Cascade equipped by gas centrifuges with regard for requirements to structural materials operating with chemically active compounds (dimethylcadmium) was devised for preparation of high-enriched cadmium isotopes. Solutions of such problems as overcoming of isotope memory, compensation of the effect of isotope overlapping, operative analytical accompanying permitted to optimize separation process and to obtain cadmium isotopes of high enrichment degree: cadmium-116 ∼98.9 %, cadmium-114 ∼98.7 %, cadmium-113 ∼93.3 %, cadmium-112 ∼99.1 %, cadmium-110 ∼95.8 %

  6. Retinoic acid induces sodium/iodide symporter gene expression and radioiodide uptake in the MCF-7 breast cancer cell line

    OpenAIRE

    Kogai, Takahiko; Schultz, James J.; Johnson, Laura S.; Huang, Min; Brent, Gregory A.

    2000-01-01

    The sodium/iodide symporter (NIS) stimulates iodide uptake in normal lactating breast, but is not known to be active in nonlactating breast or breast cancer. We studied NIS gene regulation and iodide uptake in MCF-7 cells, an estrogen receptor (ER)-positive human breast cancer cell line. All-trans retinoic acid (tRA) treatment stimulated iodide uptake in a time- and dose-dependent fashion up to ≈9.4-fold above baseline. Stimulation with selective retinoid compounds indicated that the inductio...

  7. Cadmium Stabilization Efficiency and Leachability by CdAl4O7 Monoclinic Structure.

    Science.gov (United States)

    Su, Minhua; Liao, Changzhong; Chuang, Kui-Hao; Wey, Ming-Yen; Shih, Kaimin

    2015-12-15

    This study investigated the stabilization efficiencies of using an aluminum-rich precursor to incorporate simulated cadmium-bearing waste sludge and evaluated the leaching performance of the product phase. Cadmium oxide and γ-alumina mixtures with various Cd/Al molar ratios were fired at 800-1000 °C for 3 h. Cadmium could be crystallochemically incorporated by γ-alumina into CdAl4O7 monoclinic phase and the reaction was strongly controlled by the treatment temperature. The crystal structure details of CdAl4O7 were solved and refined with the Rietveld refinement method. According to the structural refinement results, the stabilization efficiencies were quantified and expressed as a transformation ratio (TR) with optimized processing parameters. The preferred treatment temperature was found to be 950 °C for mixtures with a Cd/Al molar ratio of 1/4, as its TR value indicated the cadmium incorporation was nearly completed after a 3 h treatment scheme. Constant-pH leaching tests (CPLT) were conducted by comparing the leachability of the CdO and CdAl4O7 phases in a pH 4.0 environment. A remarkable reduction in cadmium leachability could be achieved via monoclinic CdAl4O7 structure formation to effectively stabilize hazardous cadmium in the waste stream. The CPLT and X-ray photoelectron spectroscopy (XPS) results suggested incongruent dissolution behavior during the leaching of the CdAl4O7 phase. PMID:26512873

  8. Cloud Point Extraction for Electroanalysis: Anodic Stripping Voltammetry of Cadmium.

    Science.gov (United States)

    Rusinek, Cory A; Bange, Adam; Papautsky, Ian; Heineman, William R

    2015-06-16

    Cloud point extraction (CPE) is a well-established technique for the preconcentration of hydrophobic species from water without the use of organic solvents. Subsequent analysis is then typically performed via atomic absorption spectroscopy (AAS), UV-vis spectroscopy, or high performance liquid chromatography (HPLC). However, the suitability of CPE for electroanalytical methods such as stripping voltammetry has not been reported. We demonstrate the use of CPE for electroanalysis using the determination of cadmium (Cd(2+)) by anodic stripping voltammetry (ASV). Rather than using the chelating agents which are commonly used in CPE to form a hydrophobic, extractable metal complex, we used iodide and sulfuric acid to neutralize the charge on Cd(2+) to form an extractable ion pair. This offers good selectivity for Cd(2+) as no interferences were observed from other heavy metal ions. Triton X-114 was chosen as the surfactant for the extraction because its cloud point temperature is near room temperature (22-25 °C). Bare glassy carbon (GC), bismuth-coated glassy carbon (Bi-GC), and mercury-coated glassy carbon (Hg-GC) electrodes were compared for the CPE-ASV. A detection limit for Cd(2+) of 1.7 nM (0.2 ppb) was obtained with the Hg-GC electrode. ASV with CPE gave a 20x decrease (4.0 ppb) in the detection limit compared to ASV without CPE. The suitability of this procedure for the analysis of tap and river water samples was demonstrated. This simple, versatile, environmentally friendly, and cost-effective extraction method is potentially applicable to a wide variety of transition metals and organic compounds that are amenable to detection by electroanalytical methods.

  9. Trapping radiodine, in the form of methyl iodide, on nuclear carbon

    Energy Technology Data Exchange (ETDEWEB)

    Nacapricha, D. [Mahidol Univ., Bangkok (Thailand); Taylor, C. [John Moores Univ., Liverpool (United Kingdom)

    1996-12-31

    Studies have been performed on potassium-iodide-impregnated charcoals of the type used in the nuclear industry for trapping radioiodine released during nuclear fission. The effects of various parameters on the trapping efficiency of methyl iodide have been investigated. A variation in particle size within a bulk charcoal caused poor precision in K value measurements because of differences in surface area, pore volume, and bed density, leading to differences in the deposition of the impregnant. Precision is improved by sieving the charcoal to a narrower size because smaller particles have a higher porosity. This finding is supported by surface area and pore measurements. Two methods of impregnation are compared by measuring K values and the deposition of potassium iodide. Charcoal impregnated by rotary evaporation exhibits both higher K values and higher potassium iodide contents than sprayed charcoal. Two designs of spraying drum are compared: a drum with helical vanes allows more efficient deposition and more uniform distribution of impregnant than a drum with axial vanes. A decrease in the K value with increasing humidity correlates with the available surface area. A similar correlation exists between water content and available pore volume. Aging of potassium-iodide-impregnated charcoal, caused by the formation of oxygen complexes on the surface, is associated with significant falls in K value. K values of charcoals also can be restored to at least their original values by heat treatment in the absence of air. 12 refs., 6 figs., 1 tab.

  10. [Determination of iodide, thiocyanate and perchlorate ions in environmental water by two-dimensional ion chromatography].

    Science.gov (United States)

    Lin, Li; Wang, Haibo; Shi, Yali

    2013-03-01

    A procedure for the determination of iodide, thiocyanate and perchlorate ions in environmental water by two-dimensional ion chromatography has been developed. At first the iodide, thiocyanate and perchlorate ions were separated from interfering ions by a column (IonPac AS16, 250 mm x 4 mm). The iodide ion, thiocyanate and perchlorate ions were then enriched with an enrichment column (MAC-200, 80 mm x 0.75 mm). In the 2nd-dimensional chromatography, iodide thiocyanate and perchlorate ions were separated and quantified by a capillary column (IonPac AS20 Capillary, 250 mm x 0.4 mm). The linear ranges were 0.05 -100 pg/L with correlation coefficients of 0. 999 9, and the detection limits were 0. 02 - 0.05 micro gg/L. The spiked recoveries of iodide, thiocyanate and perchlorate ions were in the range of 85.1% to 100.1%. The relative standard deviations of the recoveries were 1.7% to 4.9%.

  11. Proton and iodine-127 nuclear magnetic resonance studies on the binding of iodide by lactoperoxidase

    Energy Technology Data Exchange (ETDEWEB)

    Sakurada, J.; Takahashi, S.; Shimizu, T.; Hatano, M.; Nakamura, S.; Hosoya, T.

    1987-10-06

    Interaction of an iodide ion with lactoperoxidase was studied by the use of /sup 1/H NMR, /sup 127/I NMR, and optical difference spectrum techniques. /sup 1/H NMR spectra demonstrated that a major broad hyperfine-shifted signal at about 60 ppm, which is ascribed to the heme peripheral methyl protons, was shifted toward high field by adding KI, indicating the binding of iodide to the active site of the enzyme; the dissociation constant was estimated to be 38 mM at pH 6.1. The binding was further detected by /sup 127/I NMR, showing no competition with cyanide. Both /sup 1/H NMR and /sup 127/I NMR revealed that the binding of iodide to the enzyme is facilitated by the protonation of an ionizable group with a pK/sup a/ value of 6.0-6.8, which is presumably the distal histidyl residue. Optical difference spectra showed that the binding of an aromatic donor molecule to the enzyme is slightly but distinctly affected by adding KI. On the basis of these results, it was suggested that an iodide ion binds to lactoperoxidase outside the heme crevice but at the position close enough to interact with the distal histidyl residue which possibly mediates electron transport in the iodide oxidation reaction.

  12. Alpha-lipoic acid induces sodium iodide symporter expression in TPC-1 thyroid cancer cell line

    International Nuclear Information System (INIS)

    Introduction: Patients with metastatic thyroid cancers that do not uptake iodine need effective therapeutic option. Differentiation-inducing agents have been tried to restore functional expression of sodium iodide symporter (NIS) without success. Our objective was to assess the effect of alpha-lipoic acid (ALA), known as potential antioxidant, on expression of sodium iodide symporter in thyroid cancer cells. Methods: Human thyroid cancer-derived cell lines, TPC-1, were treated with ALA, and changes in NIS mRNA and protein expression were measured. ALA's effect on NIS gene promoter was evaluated, and functional NIS expression was assessed by iodide uptake assay. Results: Treatment with ALA increased NIS mRNA expression up to ten folds of control dose-dependently after 24 h of exposure. ALA increased NIS promoter activity, and increased iodide uptake by 1.6 fold. ALA induced expression of NIS protein, but had no significant effect on the plasma membrane trafficking. ALA increased phosphorylation of CREB and nuclear translocation of pCREB, and co-treatment of ALA and trichostatin A increased iodide uptake by three folds in TPC-1 cells. Conclusions: ALA is a potential agent to increase NIS transcription in TPC-1. It could be used as an adjunctive agent to increase efficacy of radioiodine therapy if combined with a strategy to increase NIS protein trafficking to cell membrane.

  13. Spatial mapping of cadmium zinc telluride materials properties and electrical response to improve device yield and performance

    CERN Document Server

    Van Scyoc, J M; Yoon, H; Gilbert, T S; Hilton, N R; Lund, J C; James, R B

    1999-01-01

    Cadmium zinc telluride has experienced tremendous growth in its application to various radiation sensing problems over the last five years. However, there are still issues with yield, particularly of the large volume devices needed for imaging and sensitivity-critical applications. Inhomogeneities of various types and on various length scales currently prevent the fabrication of large devices of high spectral performance. This paper discusses the development of a set of characterization tools for quantifying these inhomogeneities, in order to develop improvement strategies to achieve the desired cadmium zinc telluride crystals for detector fabrication.

  14. CH3NH3PbCl3 Single Crystals: Inverse Temperature Crystallization and Visible-Blind UV-Photodetector

    KAUST Repository

    Maculan, Giacomo

    2015-09-02

    Single crystals of hybrid perovskites have shown remarkably improved physical properties compared to their polycrystalline film counterparts, underscoring their importance in the further development of advanced semiconductor devices. Here we present a new method of sizeable CH3NH3PbCl3 single crystal growth based on retrograde solubility behavior of hybrid perovskites. We show, for the first time, the energy band structure, charge-carrier recombination and transport properties of single crystal CH3NH3PbCl3. The chloride-based perovskite crystals exhibit trap-state density, charge carriers concentration, mobility and diffusion length comparable with the best quality crystals of methylammonium lead iodide or bromide perovskites reported so far. The high quality of the crystal along with its suitable optical bandgap enabled us to design and build an efficient visible-blind UV-photodetector, demonstrating the potential of this material to be employed in optoelectronic applications.

  15. X-ray imaging performance of structured cesium iodide scintillators.

    Science.gov (United States)

    Zhao, Wei; Ristic, Goran; Rowlands, J A

    2004-09-01

    Columnar structured cesium iodide (CsI) scintillators doped with Thallium (Tl) have been used extensively for indirect x-ray imaging detectors. The purpose of this paper is to develop a methodology for systematic investigation of the inherent imaging performance of CsI as a function of thickness and design type. The results will facilitate the optimization of CsI layer design for different x-ray imaging applications, and allow validation of physical models developed for the light channeling process in columnar CsI layers. CsI samples of different types and thicknesses were obtained from the same manufacturer. They were optimized either for light output (HL) or image resolution (HR), and the thickness ranged between 150 and 600 microns. During experimental measurements, the CsI samples were placed in direct contact with a high resolution CMOS optical sensor with a pixel pitch of 48 microns. The modulation transfer function (MTF), noise power spectrum (NPS), and detective quantum efficiency (DQE) of the detector with different CsI configurations were measured experimentally. The aperture function of the CMOS sensor was determined separately in order to estimate the MTF of CsI alone. We also measured the pulse height distribution of the light output from both the HL and HR CsI at different x-ray energies, from which the x-ray quantum efficiency, Swank factor and x-ray conversion gain were determined. Our results showed that the MTF at 5 cycles/mm for the HR type was 50% higher than for the HL. However, the HR layer produces approximately 36% less light output. The Swank factor below K-edge was 0.91 and 0.93 for the HR and HL types, respectively, thus their DQE(0) were essentially identical. The presampling MTF decreased as a function of thickness L. The universal MTF, i.e., MTF plotted as a function of the product of spatial frequency f and CsI thickness L, increased as a function of L. This indicates that the light channeling process in CsI improved the MTF of

  16. Response of Saccharomyces cerevisiae to cadmium stress

    Energy Technology Data Exchange (ETDEWEB)

    Moreira, Luciana Mara Costa; Ribeiro, Frederico Haddad; Neves, Maria Jose [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil). Lab. de Radiobiologia], e-mail: luamatu@uol.com.br; Porto, Barbara Abranches Araujo; Amaral, Angela M.; Menezes, Maria Angela B.C. [Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG (Brazil). Lab. de Ativacao Neutronica], e-mail: menezes@cdtn.br; Rosa, Carlos Augusto [Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG (Brazil). Dept. de Microbiologia], e-mail: carlrosa@icb.ufmg

    2009-07-01

    The intensification of industrial activity has been greatly contributing with the increase of heavy metals in the environment. Among these heavy metals, cadmium becomes a serious pervasive environmental pollutant. The cadmium is a heavy metal with no biological function, very toxic and carcinogenic at low concentrations. The toxicity of cadmium and several other metals can be mainly attributed to the multiplicity of coordination complexes and clusters that they can form. Some aspects of the cellular response to cadmium were extensively investigated in the yeast Saccharomyces cerevisiae. The primary site of interaction between many toxic metals and microbial cells is the plasma membrane. Plasma-membrane permeabilisation has been reported in a variety of microorganisms following cadmium exposure, and is considered one mechanism of cadmium toxicity in the yeast. In this work, using the yeast strain S. cerevisiae W303-WT, we have investigated the relationships between Cd uptake and release of cellular metal ions (K{sup +} and Na{sup +}) using neutron activation technique. The neutron activation was an easy, rapid and suitable technique for doing these metal determinations on yeast cells; was observed the change in morphology of the strains during the process of Cd accumulation, these alterations were observed by Transmission Electron Microscopy (TEM) and Scanning Electron Microscopy (SEM) during incorporation of cadmium. (author)

  17. Response of Pleurotus ostreatus to cadmium exposure

    Energy Technology Data Exchange (ETDEWEB)

    Favero, N.; Bressa, G.; Costa, P. (Univ. of Padua (Italy))

    1990-08-01

    The possibility of utilizing agroindustrial wastes in the production of edible, high-quality products (e.g., mushrooms) implies the risk of bringing toxic substances, such as heavy metals, into the human food chain. Thus, growth in the presence of cadmium and cadmium accumulation limits have been studied in the industrially cultivated fungus P. ostreatus. Fruit body production is substantially unaffected in the presence of 25, 139, and 285 mg Cd/kg of dried substrate. Cadmium concentration in fruit bodies is related to cadmium substrate level, the metal being present at higher levels in caps (22-56 mg/kg dry wt) than in stems (13-36 mg/kg dry wt). Concentration factor (CF), very low in the controls (about 2), further decreases in treated specimens. The presence of a cadmium control mechanism in this fungi species is suggested. Fruit body cadmium levels could, however, represent a risk for P. ostreatus consumers, according to FAO/WHO limits related to weekly cadmium intake.

  18. Crystal Meth

    Science.gov (United States)

    ... for: Navigation Home / Stories of Hope / Crystal meth Crystal meth Story Of Hope By giovanni January 3rd, ... about my drug addiction having to deal with Crystal meth. I am now in recovery and fighting ...

  19. Performance of photomultiplier tubes and sodium iodide scintillation detector systems

    Science.gov (United States)

    Meegan, C. A.

    1981-01-01

    The performance of photomultiplier tubes (PMT's) and scintillation detector systems incorporating 50.8 by 1.27 cm NaI (T l) crystals was investigated to determine the characteristics of the photomultiplier tubes and optimize the detector geometry for the Burst and Transient Source Experiment on the Gamma Ray Observatory. Background information on performance characteristics of PMT's and NaI (T l) detectors is provided, procedures for measurement of relevant parameters are specified, and results of these measurements are presented.

  20. Quantification of propidium iodide delivery with millisecond electric pulses: A model study

    CERN Document Server

    Yu, Miao

    2014-01-01

    A model study of propidium iodide delivery with millisecond electric pulses is presented; this work is a companion of the experimental efforts by Sadik et al. [1]. Both membrane permeabilization and delivery are examined with respect to six extra-cellular conductivities. The transmembrane potential of the permeabilized regions exhibits a consistent value, which corresponds to a bifurcation point in the pore-radius-potential relation. Both the pore area density and membrane conductance increase with an increasing extra-cellular conductivity. On the other hand, the inverse correlation between propidium iodide delivery and extra-cellular conductivity as observed in the experiments is quantitatively captured by the model. This agreement confirms that this behavior is primarily mediated by electrophoretic transport during the pulse. The results suggest that electrophoresis is important even for the delivery of small molecules such as propidium iodide. The direct comparison between model prediction and experimental...

  1. Iodide retention by cinnabar (HgS) and chalcocite (Cu{sub 2}S)

    Energy Technology Data Exchange (ETDEWEB)

    Anderson, H.L.; Balsley, S.D.; Brady, P.V.

    1995-07-01

    Sorption of iodide (I{sup {minus}}) on cinnabar (HgS) and chalcocite (Cu{sub 2}S) was examined as a function of pH at 25{degrees}C in a series of batch experiments. Calculated distribution ratios (K{sub d}) far exceed those reported for other minerals; maximal K{sub d}`s of 1375 cc/g (Cu{sub 2}S) and 3080 c/g (HgS) were observed between pH 4-5, but wre substantial at all pH`s measured (4 < pH < 10). Iodide sorption apparently occurs by the formation of an insoluble surface solid solution with exposed Hg and Cu sites. Surface solid solution formation is favored at low pH due to the lessened electrostatic repulsion of the iodide ion by the sulfide surfaces.

  2. Cadmium Toxicity to Ringed Seals (Phoca hispida)

    DEFF Research Database (Denmark)

    Sonne, Christian; Dietz, R.; Riget, F. F.;

    as laboratory mammals. We have studied possible cadmium induced histopathological changes in the kidneys as well as a demineralisation of the skeletal system (DXA-scanning of lumbal vertebraes). No obvious cadmium induced toxic changes were found. Food composition and physiological adaptations may explain......Cadmium concentrations in kidneys from ringed seals (Phoca hispida) from North West Greenland (Qaanaaq) are high. Concentrations range at level known to induce renal toxic effects (mainly tubulopathy) and demineralisation (osteopenia) of the skeletal system (Fanconi's Syndrome) in humans as well...

  3. All-Solid-State Iodide Selective Electrode for Iodimetry of Iodized Salts and Vitamin C

    Directory of Open Access Journals (Sweden)

    TIRUWORK MEQUANINT

    2012-12-01

    Full Text Available A laboratory-made all-solid state iodide selective electrode, with Ag2S-AgI coated on a graphite rod recovered from dry cell battery, was prepared according to previous procedures. The electrode’s linear response to iodide was in the concentration range of 10-6 M to 10-1 M with a slope of 56.85 mV/decade and a detection limit of 6×10-7M. Iodate recovery test for laboratory formulated iodate-iodized salt was found to be 98.6 % with a standard deviation of 1.14%. The titratability of the iodized salt solution was at least 10-200 ppm potassium iodate (6-120 ppm iodine, exhibiting distinct endpoints in the range wider than the ones set in regulatory standards and reflecting that QC monitoring in production and stability decline of iodine content upon storage can be performed with the electrode method. On the basis this potentiometric titration, the application of the laboratory-made iodide electrode (vs. a saturated calomel reference electrode was extended to the determination of iodine in commercial iodized salts. In all the iodine assays, the iodate-iodized salt was initially treated with acid and an excess of iodide before titration against Na2S2O3 solution. The iodine content in table salts iodized with iodide was determined by direct potentiometry. The electrode was further used for vitamin C (ascorbic acid determinations in pharmaceutical tablets and orange juice by back titrating excess I3- against standard Na2S2O3 in acidic media. The overall outcome is that the iodide ISE can be used as sharp endpoint indicator for these titrimetric reactions in place of the well known official, but visually monitored, starch- triodide end-point reaction detection.

  4. Synthesis and characterization of some binary and ternary zirconium iodides

    Energy Technology Data Exchange (ETDEWEB)

    Guthrie, D.H.

    1981-10-01

    Studies of binary ZrI/sub 4/-Zr and ternary CsI-Zr-ZrI/sub 4/ systems have produced several new compounds. The new binary compounds include two polymorphs of ZrI/sub 2/ (..cap alpha.. and ..beta..) as well as a phase described earlier as ZrI/sub 1/ /sub 8/. ..cap alpha..-ZrI/sub 2/ forms as black lath-like crystals by vapor phase transport reactions between Zr and ZrI/sub 4/ from 700 to 825/sup 0/C. Its structure is monoclinic space group P2/sub 1//m with a = 6.821(2), b = 3.741(1), c = 14.937(3) A and ..beta.. = 95.66(3)/sup 0/, Z = 4 (R = 0.064). ..beta..-ZrI/sub 2/ is formed as black gem-like crystals between 800 to 975/sup 0/C, crystallizing in the trigonal space group R anti 3 with hexagonal axes a = 14.502(2) and c = 9.996(2) A, Z = 18 (R = 0.109). This phase contains a Zr/sub 6/I/sub 12/ cluster. Guinier x-ray powder diffraction data previously reported for ZrI/sub 1/ /sub 8/ has now been found to arise from ..cap alpha..-ZrI/sub 2/ intergrown with an orthorhombic ZrI/sub 2/ phase (perhaps isostructural with WTe/sub 2/ plus an unknown phase. The ternary compounds include Cs/sub 2/ZrI/sub 6/, Cs/sub 3/Zr/sub 2/T/sub 9/ and CsZr/sub 6/I/sub 14/. The first is isostructural with K/sub 2/PtCl/sub 6/. Cs/sub 3/Zr/sub 2/I/sub 9/ is formed from the reaction of CsI, ZrI/sub 4/ and Zr between 700 to 900/sup 0/C as black gem-like crystals which crystallize in the space group P6/sub 3//mmc with a = 8.269(1) and c = 19.908(3) A, z = 2. This phase was found to have a Cs/sub 3/Cr/sub 2/Cl/sub 9/-type structure, d/sub Zr-Zr/ = 3.134(4) A (R = 0.087). CsZr/sub 6/I/sub 14/ forms both rod and gem crystals by the same reaction with more metal between 900 to 950/sup 0/C. It crystallizes in the orthorhombic space group Ccmb with a = 14.275(4), b = 15.880(4) and c = 12.953 (4) A (R = 0.062). This phase also contains a Zr/sub 6/I/sub 12/ cluster.

  5. Modeling of Turing Structures in the Chlorite-Iodide-Malonic Acid-Starch Reaction System

    Science.gov (United States)

    Lengyel, Istivan; Epstein, Irving R.

    1991-02-01

    Recent experiments on the chlorite-iodide-malonic acid-starch reaction in a gel reactor give the first evidence of the existence of the symmetry breaking, reaction-diffusion structures predicted by Turing in 1952. A five-variable model that describes the temporal behavior of the system is reduced to a two-variable model, and its spatial behavior is analyzed. Structures have been found with wavelengths that are in good agreement with those observed experimentally. The gel plays a key role by binding key iodine species, thereby creating the necessary difference in the effective diffusion coefficients of the activator and inhibitor species, iodide and chlorite ions, respectively.

  6. Iodide uptake in human anaplastic thyroid carcinoma cells after transfer of the human thyroid peroxidase gene

    Energy Technology Data Exchange (ETDEWEB)

    Haberkom, U. [Clinical Cooperation Unit Nuclear Medicine, German Cancer Research Center, Heidelberg (Germany); Dept. of Nuclear Medicine, Univ. of Heidelberg (Germany); Altmann, A.; Jiang, S.; Morr, I.; Mahmut, M. [Clinical Cooperation Unit Nuclear Medicine, German Cancer Research Center, Heidelberg (Germany); Eisenhut, M. [Dept. of Nuclear Medicine, Univ. of Heidelberg (Germany)

    2001-05-01

    Human thyroperoxidase (hTPO) is critical for the accumulation of iodide in thyroid tissues. Poorly differentiated and anaplastic thyroid tumours which lack thyroid-specific gene expression fail to accumulate iodide and, therefore, do not respond to iodine-131 therapy. We consequently investigated whether transfer of the hTPO gene is sufficient to restore the iodide-trapping capacity in undifferentiated thyroid and non-thyroid tumour cells. The human anaplastic thyroid carcinoma cell lines C643 and SW1736, the rat Morris hepatoma cell line MH3924A and the rat papillary thyroid carcinoma cell line L2 were used as in vitro model systems. Employing a bicistronic retroviral vector based on the myeloproliferative sarcoma virus for the transfer of the hTPO and the neomycin resistance gene, the C643 cells and SW1736 cells were transfected while the L2 cells and MH3924A cells were infected with retroviral particles. Seven recombinant C643 and seven SW1736 cell lines as well as four recombinant L2 and four MH3924A cell lines were established by neomycin selection. They were studied for hTPO expression using an antibody-based luminescence kit, followed by determination of the enzyme activity in the guaiacol assay and of the iodide uptake capacity in the presence of Na{sup 125}I. Genetically modified cell lines expressed up to 1,800 times more hTPO as compared to wild type tumour cells. The level of hTPO expression varied significantly between individual neomycin-resistant cell lines, suggesting that the recombinant retroviral DNA was integrated at different sites of the cellular genome. The accumulation of iodide, however, was not significantly enhanced in individual recombinant cell lines, irrespective of low or high hTPO expression. Moreover, there was no correlation between hTPO expression and enzyme activity in individual cell lines. The transduction of the hTPO gene per se is not sufficient to restore iodide trapping in non-iodide-concentrating tumour cells. Future

  7. A Selective Iodide Ion Sensor Electrode Based on Functionalized ZnO Nanotubes

    OpenAIRE

    Magnus Willander; Zafar Hussain Ibupoto; Kimleang Khun

    2013-01-01

    In this research work, ZnO nanotubes were fabricated on a gold coated glass substrate through chemical etching by the aqueous chemical growth method. For the first time a nanostructure-based iodide ion selective electrode was developed. The ZnO nanotubes were functionalized with miconazole ion exchanger and the electromotive force (EMF) was measured by the potentiometric method. The iodide ion sensor exhibited a linear response over a wide range of concentrations (1 × 10−6 to 1 × 10−1 M) and ...

  8. Tris(1,2-dimethoxyethane-κ2O,O′iodidocalcium iodide

    Directory of Open Access Journals (Sweden)

    Siou-Wei Ou

    2012-02-01

    Full Text Available In the title complex, [CaI(C4H10O23]I, the CaII atom is seven-coordinated by six O atoms from three 1,2-dimethoxyethane (DME ligands and one iodide anion in a distorted pentagonal–bipyramidal geometry. The I atom and one of the O atoms from a DME ligand lie in the axial positions while the other O atoms lie in the basal plane. The other iodide anion is outside the complex cation.

  9. Broadband tunable hybrid photonic crystal-nanowire light emitter

    CERN Document Server

    Wilhelm, Christophe E; Xiong, Qihua; Soci, Cesare; Lehoucq, Gaëlle; Dolfi, Daniel; De Rossi, Alfredo; Combrié, Sylvain

    2015-01-01

    We integrate about 100 single Cadmium Selenide semiconductor nanowires in self-standing Silicon Nitride photonic crystal cavities in a single processing run. Room temperature measurements reveal a single narrow emission linewidth, corresponding to a Q-factor as large as 5000. By varying the structural parameters of the photonic crystal, the peak wavelength is tuned, thereby covering the entire emission spectral range of the active material. A very large spectral range could be covered by heterogeneous integration of different active materials.

  10. Efficiency enhancement in dye sensitized solar cells using gel polymer electrolytes based on a tetrahexylammonium iodide and MgI2 binary iodide system.

    Science.gov (United States)

    Bandara, T M W J; Dissanayake, M A K L; Jayasundara, W J M J S R; Albinsson, I; Mellander, B-E

    2012-06-28

    Quasi-solid-state dye-sensitized solar cells have drawn the attention of scientists and technologists as a potential candidate to supplement future energy needs. The conduction of iodide ions in quasi-solid-state polymer electrolytes and the performance of dye sensitized solar cells containing such electrolytes can be enhanced by incorporating iodides having appropriate cations. Gel-type electrolytes, based on PAN host polymers and mixture of salts tetrahexylammonium iodide (Hex4N(+)I(-)) and MgI2, were prepared by incorporating ethylene carbonate and propylene carbonate as plasticizers. The salt composition in the binary mixture was varied in order to optimize the performance of solar cells. The electrolyte containing 120% Hex4N(+)I(-) with respect to weight of PAN and without MgI2 showed the highest conductivity out of the compositions studied, 2.5 × 10(-3) S cm(-1) at 25 °C, and a glass transition at -102.4 °C. However, the electrolyte containing 100% Hex4N(+)I(-) and 20% MgI2 showed the best solar cell performance highlighting the influence of the cation on the performance of the cell. The predominantly ionic behaviour of the electrolytes was established from the dc polarization data and all the electrolytes exhibit iodide ion transport. Seven different solar cells were fabricated employing different electrolyte compositions. The best cell using the electrolyte with 100% Hex4N(+)I(-) and 20% MgI2 with respect to PAN weight showed 3.5% energy conversion efficiency and 8.6 mA cm(-2) short circuit current density.

  11. Studying Equilibrium in the Chemical Reaction between Ferric and Iodide Ions in Solution Using a Simple and Inexpensive Approach

    Science.gov (United States)

    Nikolaychuk, Pavel Anatolyevich; Kuvaeva, Alyona Olegovna

    2016-01-01

    A laboratory experiment on the study of the chemical equilibrium based on the reaction between ferric and iodide ions in solution with the formation of ferrous ions, free iodine, and triiodide ions is developed. The total concentration of iodide and triiodide ions in the reaction mixture during the reaction is determined by the argentometric…

  12. Market for nickel-cadmium batteries

    Science.gov (United States)

    Putois, F.

    Besides the lead/acid battery market, which has seen a tremendous development linked with the car industry, the alkaline rechargeable battery market has also been expanded for more than twenty years, especially in the field of portable applications with nickel-cadmium batteries. Today, nickel-cadmium batteries have to face newcomers on the market, such as nickel-metal hydride, which is another alkaline couple, and rechargeable lithium batteries; these new battery systems have better performances in some areas. This work illustrates the status of the market for nickel-cadmium batteries and their applications. Also, for two major applications—the cordless tool and the electric vehicles—the competitive situation of nickel-cadmium batteries; facing new systems such as nickel-metal hydride and lithium ion cells are discussed.

  13. RISK ASSESSMENT AND MANAGEMENT OF ENVIRONMENTAL CADMIUM

    Science.gov (United States)

    Cadmium consumed in foods grown on soils contaminated by industrial Cd+Zn discharge has caused renal tubular dysfunction in exposed humans in discrete situations. However, lack of understanding about environmental Cd has caused wide concern that generalpopulations may...

  14. Ionic and Optical Properties of Methylammonium Lead Iodide Perovskite across the Tetragonal-Cubic Structural Phase Transition

    Energy Technology Data Exchange (ETDEWEB)

    Hoque, Md Nadim Ferdous [Department of Electrical and Computer Engineering and Nano Tech Center, Texas Tech University, Lubbock Texas 79409 USA; Islam, Nazifah [Department of Electrical and Computer Engineering and Nano Tech Center, Texas Tech University, Lubbock Texas 79409 USA; Li, Zhen [Chemistry and Nanoscience Center, National Renewable Energy Laboratory, Golden Colorado 80401 USA; Ren, Guofeng [Department of Electrical and Computer Engineering and Nano Tech Center, Texas Tech University, Lubbock Texas 79409 USA; Zhu, Kai [Chemistry and Nanoscience Center, National Renewable Energy Laboratory, Golden Colorado 80401 USA; Fan, Zhaoyang [Department of Electrical and Computer Engineering and Nano Tech Center, Texas Tech University, Lubbock Texas 79409 USA

    2016-09-01

    Practical hybrid perovskite solar cells (PSCs) must endure temperatures above the tetragonal-cubic structural phase transition of methylammonium lead iodide (MAPbI3). However, the ionic and optical properties of MAPbI3 in such a temperature range, and particularly, dramatic changes in these properties resulting from a structural phase transition, are not well studied. Herein, we report a striking contrast at approximately 45 degrees C in the ionic/electrical properties of MAPbl3 owing to a change of the ion activation energy from 0.7 to 0.5 eV, whereas the optical properties exhibit no particular transition except for the steady increase of the bandgap with temperature. These observations can be explained by the 'continuous' nature of perovskite phase transition. We speculate that the critical temperature at which the ionic/electrical properties change, although related to crystal symmetry variation, is not necessarily the same temperature as when tetragonal-cubic structural phase transition occurs.

  15. Analysis of iodide and iodate in Lake Mead, Nevada using a headspace derivatization gas chromatography-mass spectrometry.

    Science.gov (United States)

    Dorman, James W; Steinberg, Spencer M

    2010-02-01

    We report here a derivatization headspace method for the analysis of inorganic iodine in water. Samples from Lake Mead, the Las Vegas Wash, and from Las Vegas tap water were examined. Lake Mead and the Las Vegas Wash contained a mixture of both iodide and iodate. The average concentration of total inorganic iodine (TII) for Lake Mead was approximately 90 nM with an iodide-to-iodate ratio of approximately 1. The TII concentration (approximately 160 nM) and the ratio of iodide to iodate were higher for the Las Vegas Wash (approximately 2). The TII concentration for tap water was close to that of Lake Mead (approximately 90 nM); however, tap water contained no detectable iodide as a result of ozonation and chlorine treatment which converts all of the iodide to iodate. PMID:19184627

  16. Some Aspects of Sealed Nickel Cadmium Cells

    Directory of Open Access Journals (Sweden)

    P. K. Saha

    1967-11-01

    Full Text Available Sealed Nickel Cadmium Cell system is termed till today as the most reliable power pack for electronic apparatus specially in low temperature use. This paper brings out the development and production of sealed nickel cadmium cells of pocket plate construction. The author who has gained experience in production of Ni-Cd cells in East Germany discusses also the major problems faced by the battery manufactures of to-day.

  17. Cadmium zinc telluride spectral modeling

    International Nuclear Information System (INIS)

    Cadmium zinc telluride (CZT) detectors are the highest resolution room temperature gamma-ray detectors available for isotopic analysis. As with germanium detectors, accurate isotopic analysis using spectra requires peak deconvolution. The CZT peak shapes are asymmetric, with a long low energy tail. The asymmetry is a result of the physics of the electron/hole transport in the semiconductor. An accurate model of the physics of the electron/hole transport through an electric field will allow the parameterization of the peak shapes as a function of energy. In turn this leads to the ability to perform accurate spectral deconvolution and therefore accurate isotopic analysis. The model and the peak-shape parameterization as a function of energy will be presented

  18. Hydrothermal Synthesis and Crystal Structure of a One-Dimensional Cadmium(Ⅱ)Complex with Isophthalic Acid and 2-Methyldipyrido[3,2-f:2′,3′-h]quinoxaline Ligands%由间苯二甲酸和喹喔啉类配体构筑的一维隔(Ⅱ)的配合物的水热合成及晶体结构

    Institute of Scientific and Technical Information of China (English)

    王蕾; 倪良; 朱(羽中); 黄艳菊

    2011-01-01

    A metal-organic coordination polymer [Cd(ipt)(Medpq)]n (H2ipt=isophthalic acid,Medpq=2-methyldipyrido[3,2-f:2′,3′-h]quinoxaline) has been hydrothermally synthesized and structurally characterized by elemental analysis,IR spectrum,UV-Vis spectrum,TG and single-crystal X-ray diffraction.Title compound crystallizes in the monoclinic system,space group C2/c,with a=2.0136(4) nm,b=1.6089(3) nm,c=1.6093(3) nm,β=125.12(3)°,V=4.3028(15) nm3,C23H18N4O6Cd,Mr=558.81,Dc=1.725 g.cm-3,Z=8,the final R=0.0531 and wR=O.1403.In the crystal structure,the cadmium is six-coordinated with four carboxylate oxygen atoms from three different carboxylate groups,and two nitrogen atoms from Medpq ligand,showing a slightly distorted octahedral geometry.Furthermore,it exhibits a one-dimensional zigzag structure with ipt-Cd-medpq as building units.CCDC:800998.%采用水热法合成了一种金属-有机配合物[Cd (ipt)(Medpq)]n(H2ipt =isophthalic acid,Medpq =2-methyldipyrido[3,2-f:2′,3′-h]quinoxaline),并对其进行了元素分析、红外光谱、紫外-可见光谱、热重表征、和X-射线单晶衍射测定.该配合物属于单斜晶系,C2/c空间群.在晶体结构中,Cd(Ⅱ)原子为六配位与来自于间苯二甲酸配体上的4个羧基氧原子,及Medpq配体上的2个氮原子配位,呈现畸变的八面体构型.整个晶体由ipt-Cd-medpq单元组成一维结构.

  19. Cadmium leaching from thermal treated and gamma irradiated Mexican aluminosilicates

    Energy Technology Data Exchange (ETDEWEB)

    Davila-Rangel, J.I. [Departamento de Quimica, Instituto Nacional de Investigaciones Nucleares, Apdo. Postal 18-1027, Mexico 11801, D.F. (Mexico); Unidad Academica Centro Regional de Estudios Nucleares, Universidad Autonoma de Zacatecas Cipres 10, Frac. La Penuela, Zacatecas, Zacatecas 98068 (Mexico); Facultad de Ciencias, Universidad Autonoma del Estado de Mexico, Instituto Literario No. 100 Col. Centro C.P. 50000, Toluca, Edo. de Mexico (Mexico); Solache-Rios, M. [Departamento de Quimica, Instituto Nacional de Investigaciones Nucleares, Apdo. Postal 18-1027, Mexico 11801, D.F. (Mexico)], E-mail: msr@nuclear.inin.mx

    2008-10-15

    Thermal and radiation effects on the leaching of cadmium from two cadmium exchanged zeolitic tuffs and one clay were determined. The cadmium exchanged aluminosilicates were heated at different temperatures (500, 700, 900 and 1100 {sup o}C), and the materials were then treated with NaCl (1 M and 5 M) and HNO{sub 3} (0.001 M and 1 M) solutions to determine the leaching behaviour of cadmium from the materials. The stability of cadmium in the materials increased as the heating temperature was increased. Cadmium leaching from gamma irradiated and heated materials at 1100 {sup o}C was higher than leaching from non-irradiated samples.

  20. Cadmium leaching from thermal treated and gamma irradiated Mexican aluminosilicates

    International Nuclear Information System (INIS)

    Thermal and radiation effects on the leaching of cadmium from two cadmium exchanged zeolitic tuffs and one clay were determined. The cadmium exchanged aluminosilicates were heated at different temperatures (500, 700, 900 and 1100 oC), and the materials were then treated with NaCl (1 M and 5 M) and HNO3 (0.001 M and 1 M) solutions to determine the leaching behaviour of cadmium from the materials. The stability of cadmium in the materials increased as the heating temperature was increased. Cadmium leaching from gamma irradiated and heated materials at 1100 oC was higher than leaching from non-irradiated samples

  1. Mercuric iodide semiconductor detectors encapsulated in polymeric resin

    Energy Technology Data Exchange (ETDEWEB)

    Martins, Joao F. Trencher; Santos, Robinson A. dos; Ferraz, Caue de M.; Oliveira, Adriano S.; Velo, Alexandre F.; Mesquita, Carlos H. de; Hamada, Margarida M., E-mail: mmhamada@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil); Disch, Christian; Fiederle, Michael [Albert-Ludwigs Universität Freiburg - UniFreibrug, Freiburg Materials Research Center - FMF, Freiburg (Germany)

    2015-07-01

    The development of new semiconductor radiation detectors always finds many setback factors, such as: high concentration of impurities in the start materials, poor long term stability, the surface oxidation and other difficulties discussed extensively in the literature, that limit their use. In this work was studied, the application of a coating resin on HgI2 detectors, in order to protect the semiconductor crystal reactions from atmospheric gases and to isolate electrically the surface of the crystals. Four polymeric resins were analyzed: Resin 1: 50% - 100%Heptane, 10% - 25% methylcyclohexane, <1% cyclohexane; Resin 2: 25% - 50% ethanol, 25% - 50% acetone, <2,5% ethylacetate; Resin 3: 50% - 100% methylacetate, 5% - 10% n-butylacetate; Resin 4: 50% - 100% ethyl-2-cyanacrylat. The influence of the polymeric resin type used on the spectroscopic performance of the HgI{sub 2} semiconductor detector is, clearly, demonstrated. The better result was found for the detector encapsulated with Resin 3. An increase of up to 26 times at the stability time was observed for the detectors encapsulated compared to that non-encapsulated detector. (author)

  2. A first-principles based study of ns2 containing ternary iodides and their possibility of scintillation

    Science.gov (United States)

    Kang, Byungkyun; Fang, C. M.; Biswas, Koushik

    2016-10-01

    A recently investigated scintillator material CsBa2I5 showed promising properties when activated with ns2 ions In+, Tl+ or the lanthanide Eu2+. This sparked our interest in an analogous group of materials, e.g. InBa2I5 or TlBa2I5 where the ns2 ion is part of the crystal framework, replacing the alkali ion. Many of these compounds of the type AB2X5 (X  =  halogen) have been previously synthesized and have interesting stereochemical activity. Using density functional calculations we have studied the stable monoclinic phase of the aforementioned ns2 containing iodides. One objective is to explore them as scintillators where the ns2 ions, now appearing as part of the crystal, play a central role. Compared to CsBa2I5, their reduced fundamental band gap and possibility of higher light yield may be attributed to an induced degree of covalency in the ns2-I bonds. The valence and conduction band edges have discernible contributions from the ns2 ions’ s and p orbitals which is crucial in carrier localization. The antibonding Ga or In s sates near valence edge may be a favored site for a hole trap, as against a {{V}k} center. Additional differences among the ns2 compounds lead to qualitatively different self-trapped excitons that may fundamentally affect luminescence. The possibility of fast electron capture at the ns2 sites and the prospect of self-activated scintillation via ns2-p  →  {{V}k} or ns2-p  →  ns2-s transitions may draw interest in related applications.

  3. Iodide-induced thyrotoxicosis in a thyroidectomized patient with metastatic thyroid carcinoma

    Energy Technology Data Exchange (ETDEWEB)

    Yoshinari, M.; Tokuyama, T.; Okamura, K.; Sato, K.; Kusuda, K.; Fujishima, M.

    1988-04-15

    An unusual case of iodide-induced thyrotoxicosis is documented in this article. The patient was a 64-year-old euthyroid man with acromegaly. He also had multiple follicular and papillary thyroid carcinomas with a metastatic lesion in the lumbar vertebrae. After a total thyroidectomy, he became slightly hypothyroid, and the lumbar lesion began to incorporate /sup 131/I by scintigraphy. When an iodine-containing contrast medium happened to be injected, a transient increase of serum thyroid hormone level was observed. After complete thyroid ablation with 83 mCi of /sup 131/I, the oral administration of 100 mg of potassium iodide for 7 days induced a prominent increase of serum thyroid hormone level. These findings indicated that the metastatic thyroid carcinoma could produce excess thyroid hormone insofar as a sufficient amount of iodide was given. Although this is the first report of such a case, iodide-induced thyrotoxicosis may not be rare in patients with thyroid carcinomas because the Wolff-Chaikoff effect is thought to be lost, and the organic iodinating activity and lysosomal protease activity are well-preserved.

  4. Reductive degradation of perfluoroalkyl compounds with aquated electrons generated from iodide photolysis at 254 nm

    OpenAIRE

    Park, Hyunwoong; vecitis, Chad D.; Cheng, Jie; Dalleska, Nathan F; Mader, Brian T.; Hoffmann, Michael R.

    2011-01-01

    The perfluoroalkyl compounds (PFCs), perfluoroalkyl sulfonates (PFXS) and perfluoroalkyl carboxylates (PFXA) are environmentally persistent and recalcitrant towards most conventional water treatment technologies. Here, we complete an in depth examination of the UV-254 nm production of aquated electrons during iodide photolysis for the reductive defluorination of six aquated perfluoroalkyl compounds (PFCs) of various headgroup and perfluorocarbon tail length. Cyclic voltammograms (CV) show tha...

  5. The sodium iodide symporter (NIS) and potential regulators in normal, benign and malignant human breast tissue.

    LENUS (Irish Health Repository)

    Ryan, James

    2011-01-01

    The presence, relevance and regulation of the Sodium Iodide Symporter (NIS) in human mammary tissue remains poorly understood. This study aimed to quantify relative expression of NIS and putative regulators in human breast tissue, with relationships observed further investigated in vitro.

  6. Relaxation of the Silver/Silver Iodide Electrode in Aqueous Solution

    NARCIS (Netherlands)

    Peverelli, K.J.

    1979-01-01

    The aim of this study is to detect and characterize relaxation processes on silver/silver iodide electrodes in aqueous electrolyte solution. The information obtained is to be used for an estimation of the consequences of similar processes on colloidal AgI particles during encounter.In chapter 1 a ge

  7. LIQUID-CRYSTALLINE AND THERMOCHROMIC BEHAVIOR OF 4-SUBSTITUTED 1-METHYLPYRIDINIUM IODIDE SURFACTANTS

    NARCIS (Netherlands)

    NUSSELDER, JJH; ENGBERTS, JBFN; VANDOREN, HA

    1993-01-01

    The mesogenic behaviour of a series of thirty-one 1-alkyl-4-(or 2-)alkyl-pyridinium salts and of a homologous series of four 1-methyl-4-n-alkoxycarbonylpyridinium iodides is described. The occurrence and stability range of the thermotropic phases depend dramatically on the structure of the surfactan

  8. Photodissociation of sodium iodide and resonant ionization of sodium atom produced

    Institute of Scientific and Technical Information of China (English)

    HUO Bing-hai; Z.T.Salim; A.H.Bakery

    2004-01-01

    Resonant ionization spectroscopy (RIS) and resonant ionization mass spectroscopy (RIMS) are employed to detect the photodissociation product of sodium iodide molecules in a molecular beam in an intense laser field in the absence of the buffer gases. Time of flight mass spectra is recorded. In particular, the appearances of multiphoton ionization are discussed.

  9. Regioselective iodination of aromatic compounds with potassium iodide in the presence of benzyltriphenylphosphonium perchlorate

    Institute of Scientific and Technical Information of China (English)

    Jalal Albadi; Masoumeh Abedini; Nasir Iravani

    2012-01-01

    A simple and efficient method for the selective iodination of various aromatic compounds by using potassium iodide in the presence of benzyltriphenylphosphonium perchlorate,is reported.This method provides several advantages such as good selectivity between ortho and para positions of aromatic compounds and high yields of the products.

  10. Kinetic modeling of the purging of activated carbon after short term methyl iodide loading

    International Nuclear Information System (INIS)

    A bimolecular reaction model containing the physico-chemical parameters of the adsorption and desorption was developed earlier to describe the kinetics of methyl iodide retention by activated carbon adsorber. Both theoretical model and experimental investigations postulated constant upstream methyl iodide concentration till the maximum break-through. The work reported here includes the extension of the theoretical model to the general case when the concentration of the challenging gas may change in time. The effect of short term loading followed by purging with air, and an impulse-like increase in upstream gas concentration has been simulated. The case of short term loading and subsequent purging has been experimentally studied to validate the model. The investigations were carried out on non-impregnated activated carbon. A 4 cm deep carbon bed had been challenged by methyl iodide for 30, 90, 120 and 180 min and then purged with air, downstream methyl iodide concentration had been measured continuously. The main characteristics of the observed downstream concentration curves (time and slope of break-through, time and amplitude of maximum values) showed acceptable agreement with those predicted by the model

  11. Ammonium-iodide route to anhydrous EuI2:mechanism and preparation

    Institute of Scientific and Technical Information of China (English)

    刁成鹏; 余金秋; 李红卫; 彭鹏; 吴浩; 何华强; 颜世宏; 胡运生

    2015-01-01

    Anhydrous EuI2 is an essential raw material for novel Eu2+-doped halide scintillators such as SrI2:Eu, CsBa2I5:Eu and BaBrI:Eu. An efficient and economic method to produce high purity anhydrous EuI2 is critical for future development and applications of these scintillators. In this paper, the ammonium-iodide route to anhydrous EuI2 was investigated, and anhydrous EuI2 with purity of 99.95 wt.%was successfully prepared. The dehydration mechanisms of europium iodide hydrate and its mixture with NH4I were comparatively investigated by X-ray diffraction (XRD), thermal analysis and fluorescence spectroscopy. The thermal decomposition process of individual europium iodide hydrate was revealed as follows:EuI3·9H2O→EuI3·8H2O→EuI3·7H2O→EuI2·H2O→EuI2, and the hydrolysis mechanism of europium hydrate was comprehensively studied. When europium iodide hydrate was dehydrated with NH4I, NH4Eu2I5 formed as an intermediate product, and the hydrolysis of EuI2 was effectively restrained. The role of NH4I as an io-dination agent was also discussed.

  12. Leaching of iodide (I(-)) and iodate (IO3(-)) anions from synthetic layered double hydroxide materials.

    Science.gov (United States)

    Theiss, Frederick L; Ayoko, Godwin A; Frost, Ray L

    2016-09-15

    Several studies have previously demonstrated that layered double hydroxides (LDHs) show considerable potential for the adsorption of radioiodine from aqueous solution; however, few studies have demonstrated that these materials are able to store radioactive (131)I for an acceptable period. The leaching of iodide (I(-)) and iodate (IO3(-)) form Mg/Al LDHs has been carried out. Contact time appeared to be a more significant variable for the leaching of iodate (IO3(-)) compared to that of iodide (I(-)). Experimental results are fitted to the pseudo second order model, suggesting that diffusion is likely to be the rate-limiting step. The presence of carbonate in the leaching solution appeared to significantly increase the leaching of iodide (I(-)) as did the presence of chloride to a lesser extent. The maximum amount of iodate (IO3(-)) leached using ultrapure water as the leaching solution was 21% of the iodate (IO3(-)) originally present. The corresponding result for iodide (I(-)) was even lower at 3%. PMID:27309951

  13. Activation of lactoperoxidase by heme-linked protonation and heme-independent iodide binding.

    Science.gov (United States)

    Toyama, Akira; Tominaga, Aya; Inoue, Tatsuo; Takeuchi, Hideo

    2010-01-01

    Lactoperoxidase (LPO), a mammalian secretory heme peroxidase, catalyzes the oxidation of thiocyanate by hydrogen peroxide to produce hypothiocyanate, an antibacterial agent. Although LPO is known to be activated at acidic pH and in the presence of iodide, the structural basis of the activation is not well understood. We have examined the effects of pH and iodide concentration on the catalytic activity and the structure of LPO. Electrochemical and colorimetric assays have shown that the catalytic activity is maximized at pH 4.5. The heme Soret absorption band exhibits a small red-shift at pH 5.0 upon acidification, which is ascribable to a structural transition from a neutral to an acidic form. Resonance Raman spectra suggest that the heme porphyrin core is slightly contracted and the Fe-His bond is strengthened in the acidic form compared to the neutral form. The structural change of LPO upon activation at acidic pH is similar to that observed for myeloperoxidase, another mammalian heme peroxidase, upon activation at neutral pH. Binding of iodide enhances the catalytic activity of LPO without affecting either the optimum pH of activity or the heme structure, implying that the iodide binding occurs at a protein site away from the heme-linked protonation site.

  14. Iodide accumulation provides kelp with an inorganic antioxidant impacting atmospheric chemistry

    Science.gov (United States)

    Küpper, Frithjof C.; Carpenter, Lucy J.; McFiggans, Gordon B.; Palmer, Carl J.; Waite, Tim J.; Boneberg, Eva-Maria; Woitsch, Sonja; Weiller, Markus; Abela, Rafael; Grolimund, Daniel; Potin, Philippe; Butler, Alison; Luther, George W.; Kroneck, Peter M. H.; Meyer-Klaucke, Wolfram; Feiters, Martin C.

    2008-01-01

    Brown algae of the Laminariales (kelps) are the strongest accumulators of iodine among living organisms. They represent a major pump in the global biogeochemical cycle of iodine and, in particular, the major source of iodocarbons in the coastal atmosphere. Nevertheless, the chemical state and biological significance of accumulated iodine have remained unknown to this date. Using x-ray absorption spectroscopy, we show that the accumulated form is iodide, which readily scavenges a variety of reactive oxygen species (ROS). We propose here that its biological role is that of an inorganic antioxidant, the first to be described in a living system. Upon oxidative stress, iodide is effluxed. On the thallus surface and in the apoplast, iodide detoxifies both aqueous oxidants and ozone, the latter resulting in the release of high levels of molecular iodine and the consequent formation of hygroscopic iodine oxides leading to particles, which are precursors to cloud condensation nuclei. In a complementary set of experiments using a heterologous system, iodide was found to effectively scavenge ROS in human blood cells. PMID:18458346

  15. Preparation and Luminescence Thermochromism of Tetranuclear Copper(I)-Pyridine-Iodide Clusters

    Science.gov (United States)

    Parmeggiani, Fabio; Sacchetti, Alessandro

    2012-01-01

    A simple and straightforward synthesis of a tetranuclear copper(I)-pyridine-iodide cluster is described as a laboratory experiment for advanced inorganic chemistry undergraduate students. The product is used to demonstrate the fascinating and visually impressive phenomenon of luminescence thermochromism: exposed to long-wave UV light, the…

  16. Reviews of the environmental effects of pollutants: IV. Cadmium

    Energy Technology Data Exchange (ETDEWEB)

    Hammons, A.S.; Huff, J.E.; Braunstein, H.M.; Drury, J.S.; Shriner, C.R.; Lewis, E.B.; Whitfield, B.L.; Towill, L.E.

    1978-06-01

    This report is a comprehensive, multidisciplinary review of the health and environmental effects of cadmium and specific cadmium derivatives. More than 500 references are cited. The cadmium body burden in animals and humans results mainly from the diet. In the United States, the normal intake of cadmium for adult humans is estimated at about 50 ..mu..g per day. Tobacco smoke is a significant additional source of cadmium exposure. The kidneys and liver together contain about 50% of the total cadmium body burden. Acute cadmium poisoning is primarily an occupational problem, generally from inhalation of cadmium fumes or dusts. In the general population, incidents of acute poisoning by inhaled or ingested cadmium or its compounds are relatively rare. The kidney is the primary target organ for toxicity from prolonged low-level exposure to cadmium. No causal relationship has been established between cadmium exposure and human cancer, although a possible link between cadmium and prostate cancer has been indicated. Cadmium has been shown to be teratogenic in rats, hamsters, and mice, but no such effects have been proven in humans. Cadmium has been reported to increase the frequency of chromosomal aberrations in cultured Chinese hamster ovary cells and in human peripheral leukocytes. The major concern about environmental cadmium is the potential effects on the general population. There is no substantial evidence of hazard from current levels of cadmium in air, water, or food. However, because cadmium is a cumulative poison and because present intake provides a relatively small safety margin, there are adequate reasons for concern over possible future increases in background levels.

  17. Reviews of the environmental effects of pollutants: IV. Cadmium

    International Nuclear Information System (INIS)

    This report is a comprehensive, multidisciplinary review of the health and environmental effects of cadmium and specific cadmium derivatives. More than 500 references are cited. The cadmium body burden in animals and humans results mainly from the diet. In the United States, the normal intake of cadmium for adult humans is estimated at about 50 μg per day. Tobacco smoke is a significant additional source of cadmium exposure. The kidneys and liver together contain about 50% of the total cadmium body burden. Acute cadmium poisoning is primarily an occupational problem, generally from inhalation of cadmium fumes or dusts. In the general population, incidents of acute poisoning by inhaled or ingested cadmium or its compounds are relatively rare. The kidney is the primary target organ for toxicity from prolonged low-level exposure to cadmium. No causal relationship has been established between cadmium exposure and human cancer, although a possible link between cadmium and prostate cancer has been indicated. Cadmium has been shown to be teratogenic in rats, hamsters, and mice, but no such effects have been proven in humans. Cadmium has been reported to increase the frequency of chromosomal aberrations in cultured Chinese hamster ovary cells and in human peripheral leukocytes. The major concern about environmental cadmium is the potential effects on the general population. There is no substantial evidence of hazard from current levels of cadmium in air, water, or food. However, because cadmium is a cumulative poison and because present intake provides a relatively small safety margin, there are adequate reasons for concern over possible future increases in background levels

  18. Cadmium removal by Lemna minor and Spirodela polyrhiza.

    Science.gov (United States)

    Chaudhuri, Devaleena; Majumder, Arunabha; Misra, Amal K; Bandyopadhyay, Kaushik

    2014-01-01

    The present study investigates the ability of two genus of duckweed (Lemna minor and Spirodela polyrhiza) to phytoremediate cadmium from aqueous solution. Duckweed was exposed to six different cadmium concentrations, such as, 0.5,1.0,1.5, 2.0, 2.5, and 3.0 mg/L and the experiment was continued for 22 days. Water samples were collected periodically for estimation of residual cadmium content in aqueous solution. At the end of treatment period plant samples were collected and accumulated cadmium content was measured. Cadmium toxicity was observed through relative growth factor and changes in chlorophyll content Experimental results showed that Lemna minor and Spirodela polyrhiza were capable of removing 42-78% and 52-75% cadmium from media depending upon initial cadmium concentrations. Cadmium was removed following pseudo second order kinetic model Maximum cadmium accumulation in Lemna minor was 4734.56 mg/kg at 2 mg/L initial cadmium concentration and 7711.00 mg/kg in Spirodela polyrhiza at 3 mg/L initial cadmium concentration at the end of treatment period. Conversely in both cases maximum bioconcentration factor obtained at lowest initial cadmium concentrations, i.e., 0.5 mg/L, were 3295.61 and 4752.00 for Lemna minor and Spirodela polyrhiza respectively. The present study revealed that both Lemna minor and Spirodela polyrhiza was potential cadmium accumulator. PMID:24933906

  19. Experimental study on iodine chemistry (EXSI) - Containment experiments with methyl iodide

    Energy Technology Data Exchange (ETDEWEB)

    Holm, J.; Ekberg, C. (Chalmers Univ. of Technology, Goeteborg (Sweden)); Kaerkelae, T.; Auvinen, A. (VTT, Espoo (Finland)); Glaenneskog, H. (Vattenfall Power Consultant, Goeteborg (Sweden))

    2011-05-15

    An experimental study on radiolytic decomposition of methyl iodide was conducted in co-operation between VTT and Chalmers University of Technology as a part of the NKS-R programs. In year 2008 the NROI project, a Nordic collaboration studying iodine chemistry in the containment, was started. During year 2008 (NROI-1) the radiolytic oxidation of elemental iodine was investigated and during 2009 (NROI-2), the radiolytic oxidation of organic iodine was studied. This project (NROI-3) is a continuation of the investigation of the oxidation of organic iodine. The project has been divided into two parts. 1. The aims of the first part were to investigate the effect of ozone and UV-radiation, in dry and humid conditions, on methyl iodide. 2. The second project was about gamma radiation (approx20 kGy/h) and methyl iodide in dry and humid conditions. 1. Experimental results showed that the methyl iodide concentration in the facility was reduced with increasing temperature and increasing UV-radiation intensity. Similar behaviour occurred when ozone was present in the system. Formed organic gas species during the decomposition of methyl iodide was mainly formaldehyde and methanol. The particle formation was instant and extensive when methyl iodide was exposed to ozone and/or radiation at all temperatures. The size of the formed primary particles was about 10 nm and the size of secondary particles was between 50-200 nm. From the SEM-EDX analyses of the particles, the conclusion was drawn that these were some kind of iodine oxides (I{sub xO{sub y}). However, the correct speciation of the formed particles was difficult to obtain because the particles melted and fused together under the electron beam. 2. The results from this sub-project are more inconsistent and hard to interpret. The particle formation was significant lesser than corresponding experiments when ozone/UV-radiation was used instead of gamma radiation. The transport of gaseous methyl iodide through the facility was

  20. Investigation on Growth and Optical Properties of LVCC Single Crystals

    Directory of Open Access Journals (Sweden)

    N. Sheen Kumar

    2014-11-01

    Full Text Available L-valine cadmium chloride (LVCC single crystals were grown by slow evaporation technique with different concentrations (0.25, 0.5, 0.75 and 1.0 mole of CdCl2. All the grown crystals were subjected to single crystal X-ray diffraction analysis. Solid state parameters were calculated for the grown crystals. The optical properties of the crystals were investigated by UV-Vis. absorption spectroscopy. The results revealed that, the wider bandgap and large transparency in the visible region along with higher polarizability of the grown crystals are highly useful in optoelectronic devices. Also according to our needs, one can tune the optical and electrical properties of LVCC crystals by adjusting the concentration of CdCl2 in LVCC.

  1. 2-Methylsulfanyl-1H-perimidin-3-ium iodide

    Directory of Open Access Journals (Sweden)

    Mohammad Hassan Ghorbani

    2012-09-01

    Full Text Available In the structure of the title salt C12H11N2S+·I−, the methylsulfanyl group of the cation is nearly coplanar with the perimidine rings, as indicated by the C—S—C—N torsion angles of 2.9 (5 and −177.2 (3°, respectively. The (SC—N bond lengths in the heterocyclic ring are approximately equal [1.325 (5 and 1.326 (6 Å] suggesting a degree of delocalization. In the crystal, cations and anions are linked via two discrete N—H...I hydrogen bonds, forming chains along the b axis.

  2. Conversion of Iodide to Hypoiodous Acid and Molecular Iodine at the Air-Water Interface

    Science.gov (United States)

    Pillar, E. A.; Guzman, M. I.

    2013-12-01

    Sea spray aerosols continuously transfer a significant amount of halides to the marine boundary layer, where they play a major role in the depletion of tropospheric ozone. The reactivity of iodide is of special interest in sea spray aerosols, where this species is enriched relative to chloride and bromide in surface seawater. This work presents laboratory experiments that provide mechanistic information to understand the reactivity of halides in atmospheric aerosols. Pneumatically assisted electrospray is used to aerosolize solutions of sodium iodide (0.01-100 μM), which are rapidly (~3 μs) oxidized by ozone at 25 °C. Reaction products include HIO, IO2-, IO3-, I2, HI2O-, and I3-, all identified by mass spectrometry. The distribution of products varies along two different reaction pathways, one favoring the production of I2 and HIO for typical tropospheric ozone levels (~50 ppbv), and another one directed to the production of IO3- at higher oxidizer concentrations. The formation of products increases exponentially with rising concentrations of initial sodium iodide, [NaI]0. The process is determined to be pH independent for the pH range 6-8 representative of surface waters. The substitution of aqueous solutions by organic solvents, such as methanol or acetonitrile, causes a decrease in the surface tension and lifetime of the droplets, leading to larger I2 production. The presence of surface active organic compounds, which alter the structure of the interfacial region, promote the pathway of I2 formation over IO3-. In conclusion, this presentation will show how the oxidation of iodide in aqueous microdroplets can release reactive gas-phase species, such as I2 and HIO, capable to affect tropospheric ozone globally. Normalized intensity of products observed during the ozonolysis of iodide solutions at 130 ppbv ozone. Cone voltage = 70 V, needle voltage = 2.5 kV.

  3. [The application of eosin and propidium iodide in evaluation of vitality of human spermatozoa].

    Science.gov (United States)

    Ploskonos, М В

    2014-11-01

    The article analyzes comparative assessment of vitality of spermatozoa by condition of permeability of membranes for eosin and propidium iodide and comparison of results acquired using technique of light and fluorescent microscopy. The comparison of data of light microscopy with eosin staining with data of fluorescent microscopy with propidium iodide staining demonstrated that percentage of content of spermatozoa separated from ejaculates of 28 fertile males and stained with eosin was reliably higher (34.8 ± 3.2) than percentage of content of spermatozoa with stained with propidium iodide (2.1 ± 4.0). After incubation of spermatozoa under room temperature during 24 hours percentage of unviable cells with stained eosin also was higher than in case of propidium iodide staining correspondingly (44.5 ± 3.3% and 34.7 ± 3.6%). The analysis of vitality of spermatozoa under damaging effect of oxidative stress on cell membrane developed by 4 hours incubation with 200 mkM of hydrogen peroxide (H2O2) demonstrated that under staining of spermatozoa with propidium iodide significantly higher percentage of damaged cells is detected. In such cases, eosin staining is less suitable for detection of vitality of spermatozoa (73.6 ± 5.8% against 51.7 ± 6.4%). The carried out experiment demonstrates that in case of detected effects on spermatozoa (for example, effect of oxidative stress) the light microscopy insufficiently adequate reflects degree of damage of membranes of spermatozoa. The fluorescent microscopy detects a higher percentage of spermatozoa with damaged membrane.

  4. Optical property of amorphous semiconductor mercury cadmium telluride from first-principles study

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    The structural and optical properties of amorphous semiconductor mercury cadmium telluride (a-MCT) are obtained by the first principles calculations. The total pair distribution functions and the density of states show that the a-MCT has the semiconductor characteristic. The calculated results of dielectric function show that E2 peak of the imaginary of dielectric function for the crystal mercury cadmium telluride abruptly disappears in the amorphous case due to the long-range disorders. And the imaginary of dielectric function of a-MCT shows a large broad peak, which is in agreement with the available results of other amorphous semiconductors. From the linear extrapolation of the curve ωε 2(ω)1/2 versus ω, it can be obtained that the optical energy gap of amorphous semiconductor Hg0.5Cd0.5Te is 0.51±0.05 eV.

  5. Optical property of amorphous semiconductor mercury cadmium telluride from first-principles study

    Institute of Scientific and Technical Information of China (English)

    WANG Liang; CHEN XiaoShuang; LU Wei; HUANG Yan; WANG XiaoFang; ZHAO JiJun

    2009-01-01

    The structural and optical properties of amorphous semiconductor mercury cadmium telluride(a-MCT) are obtained by the first principles calculations. The total pair distribution functions and the density of states show that the a-MCT has the semiconductor characteristic. The calculated results of dielectric function show that E2 peak of the imaginary of dielectric function for the crystal mercury cadmium telluride abruptly disappears in the amorphous case due to the long-range disorders. And the imaginary of dielectric function of a-MCT shows a large broad peak, which is in agreement with the available results of other amorphous semiconductors. From the linear extrapolation of the curve (n)ωε2(ω)1/2 versus (n)ω,it can be obtained that the optical energy gap of amorphous semiconductor Hg0.5Cd0.5Te is 0.51±0.05 eV.

  6. Cadmium exposure induces hematuria in Korean adults

    International Nuclear Information System (INIS)

    Introduction: Toxic heavy metals have adverse effects on human health. However, the risk of hematuria caused by heavy metal exposure has not been evaluated. Methods: Data from 4701 Korean adults were obtained in the Korean National Health and Nutritional Examination Survey (2008–2010). Blood levels of the toxic heavy metals cadmium, lead, and mercury were measured. Hematuria was defined as a result of ≥+1 on a urine dipstick test. The odds ratios (ORs) for hematuria were measured according to the blood heavy metal levels after adjusting for multiple variables. Results: Individuals with blood cadmium levels in the 3rd and 4th quartiles had a greater OR for hematuria than those in the 1st quartile group: 3rd quartile, 1.35 (1.019–1.777; P=0.037); 4th quartile, 1.52 (1.140–2.017; P=0.004). When blood cadmium was considered as a log-transformed continuous variable, the correlation between blood cadmium and hematuria was significant: OR, 1.97 (1.224–3.160; Ptrend=0.005). In contrast, no significant correlations between hematuria and blood lead or mercury were found in the multivariate analyses. Discussion: The present study shows that high cadmium exposure is associated with a risk of hematuria. -- Highlights: • A high level of blood cadmium is associated with a high risk of hematuria. • This correlation is independent of several confounding factors. • Blood levels of lead and mercury are not associated with risk of hematuria. • This is the first study on the correlation between cadmium exposure and hematuria risk

  7. Cadmium exposure induces hematuria in Korean adults

    Energy Technology Data Exchange (ETDEWEB)

    Han, Seung Seok [Department of Internal Medicine, Seoul National University College of Medicine, Seoul 110-744 (Korea, Republic of); Kim, Myounghee, E-mail: dkkim73@gmail.com [Department of Dental Hygiene, College of Health Science, Eulji University, Gyeonggi-do 461-713 (Korea, Republic of); Lee, Su Mi [Department of Internal Medicine, Seoul National University College of Medicine, Seoul 110-744 (Korea, Republic of); Lee, Jung Pyo [Department of Internal Medicine, Seoul National University Boramae Medical Center, Seoul 156-707 (Korea, Republic of); Kim, Sejoong [Department of Internal Medicine, Seoul National University Bundang Hospital, Gyeonggi-do 463-707 (Korea, Republic of); Joo, Kwon Wook [Department of Internal Medicine, Seoul National University College of Medicine, Seoul 110-744 (Korea, Republic of); Lim, Chun Soo [Department of Internal Medicine, Seoul National University Boramae Medical Center, Seoul 156-707 (Korea, Republic of); Kim, Yon Su; Kim, Dong Ki [Department of Internal Medicine, Seoul National University College of Medicine, Seoul 110-744 (Korea, Republic of)

    2013-07-15

    Introduction: Toxic heavy metals have adverse effects on human health. However, the risk of hematuria caused by heavy metal exposure has not been evaluated. Methods: Data from 4701 Korean adults were obtained in the Korean National Health and Nutritional Examination Survey (2008–2010). Blood levels of the toxic heavy metals cadmium, lead, and mercury were measured. Hematuria was defined as a result of ≥+1 on a urine dipstick test. The odds ratios (ORs) for hematuria were measured according to the blood heavy metal levels after adjusting for multiple variables. Results: Individuals with blood cadmium levels in the 3rd and 4th quartiles had a greater OR for hematuria than those in the 1st quartile group: 3rd quartile, 1.35 (1.019–1.777; P=0.037); 4th quartile, 1.52 (1.140–2.017; P=0.004). When blood cadmium was considered as a log-transformed continuous variable, the correlation between blood cadmium and hematuria was significant: OR, 1.97 (1.224–3.160; P{sub trend}=0.005). In contrast, no significant correlations between hematuria and blood lead or mercury were found in the multivariate analyses. Discussion: The present study shows that high cadmium exposure is associated with a risk of hematuria. -- Highlights: • A high level of blood cadmium is associated with a high risk of hematuria. • This correlation is independent of several confounding factors. • Blood levels of lead and mercury are not associated with risk of hematuria. • This is the first study on the correlation between cadmium exposure and hematuria risk.

  8. Hazards to wildlife from soil-borne cadmium reconsidered

    Science.gov (United States)

    Beyer, W.N.

    2000-01-01

    Cadmium is a toxic element that should be included in environmental risk assessments of contaminated soils. This paper argues, however, that hazards to wildlife from cadmium have often been overstated. The literature contains only meager evidence that wild animals have been seriously harmed by cadmium, even at severely contaminated sites. Although some researchers have reported that wildlife have accumulated concentrations of cadmium in their kidneys that were above suggested injury thresholds, the thresholds may be disputed, since they were well below the World Health Organization criterion of 200 mg/kg (wet weight) of cadmium in the renal cortex for protecting human health. Recent risk assessments have concluded that soil cadmium concentrations less than 1 mg/kg are toxic to soil organisms and wildlife, which implies that background concentrations of cadmium naturally found in soils are hazardous. An examination of the databases used to support these assessments suggested that the toxicity of cadmium has been exaggerated.

  9. Synergistic Effect of Azadirachta Indica Extract and Iodide Ions on the Corrosion Inhibition of Aluminium in Acid Media

    International Nuclear Information System (INIS)

    The synergistic action caused by iodide ions on the corrosion inhibition of aluminium (Al) in 0.5 M HCl in the presence of Azadirachta Indica (AZI) plant extract has been investigated using potintiodynamic polarization and impedance techniques. It is found that AZI extract inhibits the corrosion of aluminium in 0.5 M HCl. The inhibition efficiency increases with the increase in AZI extract concentration, until 24% v/v of AZI extract, then Inh.% is decreased with father increase in AZI extract concentration. The adsorption of this extract in the studied concentration is found to obey Frewendlish adsorption isotherm. The addition of iodide ions enhances the inhibition efficiency to a considerable extent. The increase in Inh.% values in presence of fixed concentration of iodide ions indicates that AZI extract forms an insoluble complex at lower AZI extract concentrations by undergoing a joint adsorption. But at higher concentrations of AZI extract, competitive adsorption is found between iodide ions and the formed complex leading to less Inh.%. The Inh.% decreased in presence of iodide ions with AZI extract than in presence of AZI extract alone at all studied iodide concentrations. The synergism parameter S θ is defined and calculated from surface coverage values. This parameter in the case of AZI extract is found to be more than unity, indicating that the enhanced inhibition efficiency caused by the addition of iodide ions

  10. Contrasting the surface ocean distribution of bromoform and methyl iodide; implications for boundary layer physics, chemistry and climate

    Energy Technology Data Exchange (ETDEWEB)

    Palmer, C J, E-mail: carl.j.palmer@gmail.co [Department of Oceanography, University of Cape Town, 7701 (South Africa)

    2010-08-15

    Bromoform and methyl iodide are both methane-like hydrocarbons with a halogen atom replacing one or more of the hydrogen atoms. Both of these compounds occur naturally in the environment as a result of their production from seaweed and kelp. They are of interest to climate science as a result of their catalytic destruction of boundary layer ozone (a potent greenhouse gas) and, specifically for methyl iodide, the proposed role in the formation of new cloud condensation nuclei with implications for climate. In this paper, the currently available data on the distribution of bromoform and methyl iodide are analysed and contrasted to show that the concentrations of bromoform and methyl iodide do not correlate, that, in contrast to bromoform, the parameterization of sea surface methyl iodide concentrations demands only the sea surface temperature, and that the pelagic distribution of methyl iodide appears to follow the solar zenith angle. These three observations together suggest that, while the pelagic source of bromoform is mostly biogenic, the source of methyl iodide is photochemical. This has implications for the understanding of planetary boundary layer chemistry and potential organohalogen mediated feedbacks to climate.

  11. Contrasting the surface ocean distribution of bromoform and methyl iodide; implications for boundary layer physics, chemistry and climate

    International Nuclear Information System (INIS)

    Bromoform and methyl iodide are both methane-like hydrocarbons with a halogen atom replacing one or more of the hydrogen atoms. Both of these compounds occur naturally in the environment as a result of their production from seaweed and kelp. They are of interest to climate science as a result of their catalytic destruction of boundary layer ozone (a potent greenhouse gas) and, specifically for methyl iodide, the proposed role in the formation of new cloud condensation nuclei with implications for climate. In this paper, the currently available data on the distribution of bromoform and methyl iodide are analysed and contrasted to show that the concentrations of bromoform and methyl iodide do not correlate, that, in contrast to bromoform, the parameterization of sea surface methyl iodide concentrations demands only the sea surface temperature, and that the pelagic distribution of methyl iodide appears to follow the solar zenith angle. These three observations together suggest that, while the pelagic source of bromoform is mostly biogenic, the source of methyl iodide is photochemical. This has implications for the understanding of planetary boundary layer chemistry and potential organohalogen mediated feedbacks to climate.

  12. On the effect of thallium additions on cadmium amalgam potentials

    International Nuclear Information System (INIS)

    A study has been made of the influence of additives of thallium on potentials of cadmium amalgams with thallium contents of 10, 20, 30, and 40 at.% at 20, 40, 60, and 80 deg C. Additives of thallium have been found to shift the potential of cadmium amalgams towards the range of negative values which indicates an increase in the activity of cadmium. A possibility of calculation of the potential shift for heterogeneous cadmium amalgams on introducing thallium has been shown

  13. Recycling of Spent Nickel-Cadmium Batteries

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    A technique for recycling spent nickel-cadmium batteries, which makes separation of cadmium and nickel possible, is developed by laboratory-scale experiments. NH3-H2CO3 aqueous solution was used in this leaching technique. Since neutralization and/or solvent extraction were not required in the separation procedure of nickel and cadmium, the closed systemization of the process becomes possible. Experimental results show that, (1) if the NH3 concentration of leaching solution is sufficiently high and the ratio of H2CO3 to NH3 is properly adjusted, both Ni(OH)2 and Cd(OH)2 react with NH3 and quickly dissolve into leaching solution, and (2) Ni(OH)2 can be converted into insoluble NiO by calcination at 500€癈, and CdO from Cd(OH)2 by calcination maintains good solubility in NH3-H2CO3 aqueous solution. As a conclusion, the recycling technique characterized by two step leaching can be developed based on such changes in dissolution behavior by calcination. Meanwhile, the yields of 99.8% for nickel and 97.6% for cadmium are obtained, and the purities of recovered nickel and cadmium are 99.9% and 98.6%, respectively.

  14. Synthesis of cholesteryl-α-D-lactoside via generation and trapping of a stable β-lactosyl iodide

    Science.gov (United States)

    Davis, Ryan A.; Fettinger, James C.; Gervay-Hague, Jacquelyn

    2015-01-01

    The generation of β-lactosyl iodide was carried out under non-in situ-anomerization, metal free conditions by reacting commercially available β-per-O-acetylated lactose with trimethylsilyl iodide (TMSI). The β-iodide was surprisingly stable as evidenced by NMR spectroscopy. Introduction of octanol or cholesterol under microwave conditions gave high yields of α-linked glycoconjugates. Careful analysis of the reaction products and mechanistic considerations suggest an acid catalyzed rearrangement that provides α-linked glycosylation products with a free C2-hydroxyl. Accessibility to these compounds may further advance glycolipidomic profiling of immune modulating bacterial derived-glycans. PMID:26543257

  15. Effect of anions on Toxicity of Cadmium Applied to MIcrobial Biomass in Red Soil

    Institute of Scientific and Technical Information of China (English)

    K.S.KHAN; XIEZHENGMIAO; 等

    1997-01-01

    A laboratory incubation experiment was conducted to elucidat the effects of associated anions on toxicity of cadmium applied to microbial biomass in the red soil. Cadmium was applied at six different levels,i.e.,O(background),5,15,30,60 and 100μg g-1 soil in the form of either cadmium acetate or cadmium chloride. Application of cadmium as cadmium acetate markedly reduced the soil microbial biomass carbon compared to cadmium applied as cadmium chlorde at all the tested levels.Similarly,organic carbon to biomass carbon ration in the soil was markedly increased by increasing the level of the cadmium in the soil as cadmium acetate,while the change wa much smaller in the case of cadmium chloride at the same cadmium levels.The results suggested that due consideration should be given to the source of cadmium while deciding the cadmium levles in experiments.

  16. Cadmium induces cadmium-tolerant gene expression in the filamentous fungus Trichoderma harzianum.

    Science.gov (United States)

    Cacciola, Santa O; Puglisi, Ivana; Faedda, Roberto; Sanzaro, Vincenzo; Pane, Antonella; Lo Piero, Angela R; Evoli, Maria; Petrone, Goffredo

    2015-11-01

    The filamentous fungus Trichoderma harzianum, strain IMI 393899, was able to grow in the presence of the heavy metals cadmium and mercury. The main objective of this research was to study the molecular mechanisms underlying the tolerance of the fungus T. harzianum to cadmium. The suppression subtractive hybridization (SSH) method was used for the characterization of the genes of T. harzianum implicated in cadmium tolerance compared with those expressed in the response to the stress induced by mercury. Finally, the effects of cadmium exposure were also validated by measuring the expression levels of the putative genes coding for a glucose transporter, a plasma membrane ATPase, a Cd(2+)/Zn(2+) transporter protein and a two-component system sensor histidine kinase YcbA, by real-time-PCR. By using the aforementioned SSH strategy, it was possible to identify 108 differentially expressed genes of the strain IMI 393899 of T. harzianum grown in a mineral substrate with the addition of cadmium. The expressed sequence tags identified by SSH technique were encoding different genes that may be involved in different biological processes, including those associated to primary and secondary metabolism, intracellular transport, transcription factors, cell defence, signal transduction, DNA metabolism, cell growth and protein synthesis. Finally, the results show that in the mechanism of tolerance to cadmium a possible signal transduction pathway could activate a Cd(2+)/Zn(2+) transporter protein and/or a plasma membrane ATPase that could be involved in the compartmentalization of cadmium inside the cell. PMID:26349455

  17. Cadmium-113m as a biogeochemical tracer for cadmium in Lake Michigan

    International Nuclear Information System (INIS)

    The Lake Michigan watershed has been sampled for 113mCd. This long-lived metastable isotope of cadmium allowed independent evaluation of cadmium distribution in this dynamic ecosystem. 113mCd analysis was not hampered by contamination or loss. These are problems which have plagued stable cadmium measurements. Sensitivity and specificity were necessary concerns. 113mCd has been preconcentrated from large samples in order to obtain sufficient activity for quantification. Specificity for the gross beta activity measured was secured in a rigorous ion exchange decontamination. Confirmation of the suspected 113mCd beta source was checked by reverse tracer analysis and modified Feather analysis range-energy relationships. The 113mCd activities confirm the expected semiconservative behavior for cadmium. This behavior manifests itself in a long residence time for cadmium in Lake Michigan. The inefficiency of outflow removal, the low sedimentation rate and the unquantified sediment resuspension and release of cadmium are factors contributing to this residence time. Steady state concentration of cadmium in Lake Michigan will increase if present input rates persist

  18. pH-Dependent Assembly and Conversions of Six Cadmium(II)-Based Coordination Complexes

    Energy Technology Data Exchange (ETDEWEB)

    Fang, Hua-Cai; Zhu, Ji-Qin; Zhou, Li-Jiang; Jia, Hong-Yang; Li, Shan-Shan; Gong, Xue; Li, Shu-Bin; Cai, Yue-Peng; Thallapally, Praveen K.; Liu, Jun; Exarhos, Gregory J.

    2010-07-07

    Six cadmium(II) complexes containing N2O2 donor tetradentate asymmetrical Schiff base ligand 2-{[2-(dimethylamino)ethylimino]methyl}-6-methoxyphenol (HL5), namely, [(Cd3L52Cl4)2]•CH3OH•H2O (1), [Cd(L5)Cl]2•CH3OH (2), [Cd2(HL5)Cl4]n (3), {[Cd3(H2L5)2Cl8]•2H2O}n (4), [(H2L5)2]2+•[CdCl4]2-•H2O (5), and [(H2L5)2]2+•[CdCl4]2- (6), have been synthesized using cadmium(II) chloride and asymmetrical Schiff base ligand HL5 under different pH conditions at room temperature. The diverse structures show the marked sensitivity of the structural chemistry of the tetradentate asymmetrical Schiff base ligand HL5. Complex 1 formed at pH = 10 exhibits a rare zero- dimensional structure of trinuclear cadmium (II). At pH = 8-9, a dinuclear cadmium (II) complex 2 is formed. The reaction at pH = 5-7 leads to two one-dimensional structures of 3 and 4. A further decrease of the pH to 3-5 results in a zero-dimensional structure 5. Owing to the departure of lattice water molecules in the crystal, complex 5 at room temperature can gradually undergo single-crystal-to-single-crystal transformation to result complex 6. The results further show that conversions of complex 1 to 5 can also be achieved by adjusting the pH value of the reaction solution, 1→2pH=8→5pH=3 and 3→4pH=5. Comparing these experimental results, it is clear that the pH plays a crucial role in the formation of the resulting structures, which simultaneously provide very effective strategies for constructing the CdII compounds with N2O2 donor tetradentate asymmetrical Schiff base ligand. The strong fluorescent emissions of the six compounds (1-6) make them potentially useful photoactive materials. Furthermore, six Schiff base cadmium complexes (1–6), with DPPH (2,2-dipheny1-1-picrylhydrazy1) as a co-oxidant exhibited the stronger scavenging activity.

  19. Part I. Voltammetric studies of potassium iodide at gold and platinum electrodes. Part II. Electrodeposition and characterization of poly(vinylferrocene) films

    Energy Technology Data Exchange (ETDEWEB)

    Holt, R.J.

    1993-01-01

    A mechanism for the adsorption of iodide on platinum and gold has been proposed in the literature which assumes hydrogen gas is evolved along with an adsorbed iodide atom. A rotating platinum ring-disk electrode was used here to detect the presence of any hydrogen produced upon iodide adsorption. No evidence for hydrogen formation was found. A gold-gold/platinum gas permeable double membrane electrode also did not show any evidence of hydrogen gas produced at gold during iodide adsorption. The voltammetry of iodide and iodate was examined using both gold and platinum ring-disk electrodes and a gas permeable double membrane electrode. The oxidation of adsorbed iodide was examined. The successful determination of the various oxidation states of iodide in acid media were performed: I[sub 2], IO[sup [minus

  20. Experimental study on iodine chemistry (EXSI) - Containment experiments with methyl iodide

    Energy Technology Data Exchange (ETDEWEB)

    Holm, J.; Glaenneskog, H.; Ekberg, C. (Chalmers Univ. of Technology (Sweden)); Kaerkelae, T.; Auvinen, A. (VTT Technical Research Centre of Finland (Finland))

    2010-05-15

    An experimental study on radiolytic decomposition of methyl iodide was conducted in co-operation between VTT and Chalmers University of Technology as a part of the NKS-R programs. The behaviour of iodine during a severe accident has been studied in several experimental programs, ranging from the large-scale PHEBUS FP tests and intermediate-scale ThAI tests to numerous separate effect studies. In year 2008 the NROI project, a Nordic collaboration studying iodine chemistry in the containment was started. During 2009, oxidation of iodine, especially organic iodine, was studied within the NROI project. The chemistry of organic iodine in the gas phase is still one of the greatest remaining uncertainties concerning iodine behaviour during a severe accident. During the first year of the NROI project the oxidation of elemental iodine, I2, with ozone and UV-light was investigated. In this study organic iodide, in this case methyl iodide, was investigated in similar conditions as in the NROI-1 project. The experimental facility applied in this study is based on the sampling system built at VTT for the ISTP project CHIP conducted by IRSN. The experimental facility and the measuring technology are sophisticated and unique in the area of nuclear research as well as in the field of aerosol science. Experimental results showed that the methyl iodide concentration in the facility was reduced with increasing temperature and increasing UVC intensity. Similar behaviour occurred when ozone was present in the system. Formed organic gas species during the decomposition of methyl iodide was mainly formaldehyde and methanol. Instant and extensive particle formation occurred when methyl iodide was transported through a UVC radiation field and/or when ozone was present. The size of the formed primary particles was about 10 nm and the size of secondary particles was between 50-150 nm. From the SEM-EDX analyses of the particles, the conclusion was drawn that these were some kind of iodine

  1. 有机二磺酸镉配合物%Organic-Disulfonate Ligand Cadmium(Ⅱ) Coordination Compound

    Institute of Scientific and Technical Information of China (English)

    谢永荣; 叶琼

    2005-01-01

    The crystal structure of [Cd(DBDA)(phen)2(H2O)](H2O)2 (1) (DBDA=2,2'-dimethoxy-1,1'-binaphthylene6,6'-disulfonate, phen=1,10-phenanthroline) composes of a cadmium center which is surrounded by four nitrogenatoms from 1,10-phenathroline as well as two oxygen atoms from water and sulfonate group of DBDA that also participates in H-bonding interactions to form 3D network. CCDC: 277920.

  2. Reduction of Cadmium Uptake of Rice Plants Using Soil Amendments in High Cadmium Contaminated Soil: A Pot Experiment

    Directory of Open Access Journals (Sweden)

    Dian Siswanto

    2013-05-01

    Full Text Available The aims of this study were to investigate the effect of agricultural residues on reducing cadmium uptake in rice plants. The rice plants growing on no cadmium/free cadmium soils (N, Cd soils (Cds, and Cd soils each amended with 1% w/w of coir pith (CP, coir pith modified with sodium hydroxide (CPm and corncob (CC under high cadmium contaminated soil with an average 145 mg Cd kg-1 soil were investigated. The results showed that the cumulative transpiration of rice grown in various treatments under high cadmium contaminated soil followed the order: Cds > CPm ≥ CP ≥ CC. These transpirations directly influenced cadmium accumulation in shoots and husks of rice plants. The CC and CP seemed to work to reduce the cadmium uptake by rice plants indicated by accumulated cadmium in the husk that were 2.47 and 7.38 mg Cd kg-1 dry weight, respectively. Overall, transpiration tended to drive cadmium accumulation in plants for rice grown in high cadmium contaminated soil. The more that plants uptake cadmium, the lower cadmium that remains in the soil.

  3. Bireactor Electronuclear Systems with Liquid Cadmium Valve

    CERN Document Server

    Bznuni, S A; Zhamkochyan, V M; ASosnin, A N; Polanski, A; Khudaverdyan, A H

    2002-01-01

    Three main types of bireactor electronuclear systems are discussed. From the point of view of assuring high level of functional characteristics and safety bireactor electronuclear systems with booster using enriched uranium (20 %) and with a liquid cadmium valve appears to be the most effective. It is shown by means of Monte-Carlo modeling that such operation conditions can be achieved which lead to the destruction of the intermediate cadmium layer making the systems supercritical (k_{eff}>1). One can avoid the problem by using a special design of the liquid cadmium valve. In comparison with other nuclear systems (critical reactors, one-reactor electronuclear systems) cascade electronuclear systems have essential advantages allowing the decrease of the proton beam current by one order of magnitude and providing at same time the necessary level of power generation and neutron flux. Availability of both the thermal and fast cones allows one to transmute not only transuranics but also the fission products - cesi...

  4. ELECTROKINETIC REMEDIATION STUDY FOR CADMIUM CONTAMINATED SOIL

    Directory of Open Access Journals (Sweden)

    P. Bala Ramudu

    2007-09-01

    Full Text Available This paper presents the results of an experimental research undertaken to evaluate different purging solutions to enhance the removal of cadmium from spiked contaminated field soil by electrokinetic remediation. Three experiments were conducted when soil was saturated with deionised water and subsequently deionised water, ammonium citrate and sodium citrate were used as purging solutions at anode end. One experiment was conducted when the soil was saturated with ammonium citrate and itself was used as the purging solution. Results showed that 49% reduction of cadmium concentration was achieved in the case of soil saturated (washed with ammonium citrate as well as purging solution also was ammonium citrate. The soil pH and washing solutions were the most important factors in controlling the removal of cadmium in electrokinetic remediation process.

  5. Plausible molecular and crystal structures of chitosan/HI type II salt.

    Science.gov (United States)

    Lertworasirikul, Amornrat; Noguchi, Keiichi; Ogawa, Kozo; Okuyama, Kenji

    2004-03-15

    Chitosan/HI type II salt prepared from crab tendon was investigated by X-ray fiber diffraction. Two polymer chains and 16 iodide ions (I(-)) crystallized in a tetragonal unit cell with lattice parameters of a = b = 10.68(3), c (fiber axis) = 40.77(13) A, and a space group P4(1). Chitosan forms a fourfold helix with a 40.77 A fiber period having a disaccharide as the helical asymmetric unit. One of the O-3... O-5 intramolecular hydrogen bonds at the glycosidic linkage is weakened by interacting with iodide ions, which seems to cause the polymer to take the 4/1-helical symmetry rather than the extended 2/1-helix. The plausible orientations of two O-6 atoms in the helical asymmetric unit were found to be gt and gg. Two chains are running through at the corner and the center of the unit cell along the c-axis. They are linked by hydrogen bonds between N-21 and O-61 atoms. Two out of four independent iodide ions are packed between the corner chains while the other two are packed between the corner and center chains when viewing through the ab-plane. The crystal structure of the salt is stabilized by hydrogen bonds between these iodide ions and N-21, N-22, O-32, O-61, O-62 of the polymer chains.

  6. Increased cadmium and lead uptake of a cadmium hyperaccumulator tomato by cadmium-resistant bacteria.

    Science.gov (United States)

    He, Lin-Yan; Chen, Zhao-Jin; Ren, Gai-Di; Zhang, Yan-Feng; Qian, Meng; Sheng, Xia-Fang

    2009-07-01

    Two cadmium (Cd)-resistant strains Pseudomonas sp. RJ10 and Bacillus sp. RJ16 were investigated for their effects on the soil Cd and lead (Pb) solubilization and promotion of plant growth and Cd and Pb uptakes of a Cd-hyperaccumulator tomato. In the heavy metal-contaminated inoculated soil, the CaCl(2)-extractable Cd and Pb were increased by 58-104% and 67-93%, respectively, compared to the uninoculation control. The bacteria produced indole acetic acid, siderophore and 1-aminocyclopropane-1-carboxylate deaminase. Root elongation assay conducted on tomato under gnotobiotic conditions demonstrated increase in root elongation of inoculated tomato seedlings compared to the control plants. An increase in Cd and Pb contents of above-ground tissues varied from 92% to 113% and from 73% to 79% in inoculated plants growing in heavy metal-contaminated soil compared to the uninoculation control, respectively. These results show that the bacteria could be exploited for bacteria enhanced-phytoextraction of Cd- and Pb-polluted soils. PMID:19368973

  7. Treatment of cadmium dust with two-stage leaching process

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    The treatment of cadmium dust with a two-stage leaching process was investigated to replace the existing sulphation roast-leaching processes. The process parameters in the first stage leaching were basically similar to the neutralleaching in zinc hydrometallurgy. The effects of process parameters in the second stage leaching on the extraction of zincand cadmium were mainly studied. The experimental results indicated that zinc and cadmium could be efficiently recoveredfrom the cadmium dust by two-stage leaching process. The extraction percentages of zinc and cadmium in two stage leach-ing reached 95% and 88% respectively under the optimum conditions. The total extraction percentage of Zn and Cdreached 94%.

  8. Cadmium toxicity in the free-living nematode, Caenorhabditis elegans

    Energy Technology Data Exchange (ETDEWEB)

    Popham, J.D.; Webster, J.M.

    1979-10-01

    The effect of cadmium on the fecundity, growth, and fine structure of the free-living nematode Caenorhabditis elegans was studied. High concentrations of cadmium significantly decreased the fecundity and growth of these organisms. Electron microscopy showed that cadmium modifies the structure of the mitochondria in the esophagus and intestine, causes the formation of inclusion bodies in the nucleus of esophageal cells, and alters the morphology of cytosomes in the intestinal cells. The results suggest that the decreased fecundity and growth of cadmium-exposed C. elegans may be due to cadmium interfering with nutrient uptake or assimilation or both.

  9. Thermodynamic properties of cadmium in lead amalgam dilute solution

    International Nuclear Information System (INIS)

    Investigation of thermodynamic properties of cadmium dilute solutions in lead amalgam is carried out by means of electromotive force technique within 453-523 K temperature range. Cadmium thermodynamic functions are calculated: activity, activity ratio, Libbs partial energy and its excess value and integral characteristics, respectively. When changing cadmium content from 0.01 up to 0.1 χcd at T=473 K, logarithm of activity ratio does not depend on alloy composition, that is, Heury's law is fulfilled. Increase of cadmium content in amalgam results in the essential reduction of mercury and cadmium reaction

  10. Urinary excretion of cadmium and zinc among persons from Sweden

    Energy Technology Data Exchange (ETDEWEB)

    Elinder, C.G.; Kjellstrom, T.; Linnman, L.; Pershagen, G.

    1978-06-01

    Cadmium and zinc concentrations in the urine of 132 Swedes, including 50 pairs of identical twins, were measured. Atomic absorption spectrophotometry procedures were developed for the analysis. Cadmium concentration increased with age and was higher among smokers than among nonsmokers. Estimated 24-hr excretion of cadmium among nonsmokers increased from about 0.25 to 0.40 ..mu..g in persons from 20 to 70 years old. The 24-hr cadmium excretions among nonsmokers in different age-groups fitted better to total kidney burden than to daily cadmium intake from food. Zinc excretion, on the other hand, decreased after the age of 20.

  11. Simple inorganic complexes but intricate hydrogen bonding networks: Synthesis and crystal structures of [MII(opda)2(NO3)2] (M = Zn and Cd; opda = orthophenylenediamine)

    Indian Academy of Sciences (India)

    Sabbani Supriya

    2009-03-01

    The compounds [ZnII{C6H4(NH2)2}2(NO3)2], (1) and [CdII{C6H4(NH2)2}2(NO3)2] (2) have been prepared (C6H4(NH2)2 = orthophenylenediammine = opda) and characterized by routine spectroscopic methods and single crystal X-ray diffraction analysis. Compound 1 crystallizes in orthorhombic space group , where as compound 2 crystallizes in monoclinic space 21/. In the crystal structure of 1 an extended hydrogen bonding network is formed involving zinc coordinated amines and nitrato ligands. The compound 2 consists of molecules in which the cadmium ion is eight coordinated, with two bidentate nitrate groups and two bidentate opda ligands. The geometry around the cadmium described as a distorted dodecahedron. The crystal structure of 2 shows an intricate hydrogen bonding network, formed by amine and nitro groups coordinated to cadmium.

  12. Syntheses and structural characterization of new dithiophosphinato cadmium complexes

    Indian Academy of Sciences (India)

    Ertuğrul Gazi̇ Sağlam; Nurcan Acar; Yasemi̇n Süzen; Berline Mougang-Soumé; Tuncer Hökelek

    2015-09-01

    New cadmium complexes of 4-methoxyphenyl dithiophosphinic acids, H3CO-C6H4-(R)PS2H were prepared. The five dithiophosphinato ligands (L) involved were of the general structure H3CO-C6H4-(R)PS2−with R= 3-methylbutyl, (L1); n-butyl, (L2); 2-methylpropyl, (L3); 1-methylpropyl, (L4) and 2-propyl, (L5).To the best of our knowledge, this is the first report on the preparation and characterization of the n-butyl-derivative. The acid forms of the ligands were obtained by treatment of the Lawesson reagent, (LR) [2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-disulfide] with the corresponding Grignard reagent in dry diethylether. The acids formed were transformed into easily crystallizable ammonium salts (NH4L) for purification. These salts were treated with CdCl2 in ethanol at room temperature to produce the bis-dithiophosphinato cadmium complexes ([Cd(L)2]2) exclusively. The structures of the complexes were elucidated by elemental analysis, MS, FTIR and Raman spectroscopy techniques as well as 1H-, 13C- and 31P- NMR. The crystal structures of [Cd(L1)2]2 and [Cd(L2)2]2 were also studied as examples. X-ray studies confirmed the nonplanar, four-coordination geometry of the complexes and indicate that electron delocalization prevails in the PS$_{−}^{2}$ moiety of the dithiophosphinato groups.

  13. Cadmium telluride quantum dots advances and applications

    CERN Document Server

    Donegan, John

    2013-01-01

    Optical Properties of Bulk and Nanocrystalline Cadmium Telluride, Núñez Fernández and M.I. VasilevskiyAqueous Synthesis of Colloidal CdTe Nanocrystals, V. Lesnyak, N. Gaponik, and A. EychmüllerAssemblies of Thiol-Capped CdTe Nanocrystals, N. GaponikFörster Resonant Energy Transfer in CdTe Nanocrystal Quantum Dot Structures, M. Lunz and A.L. BradleyEmission of CdTe Nanocrystals Coupled to Microcavities, Y.P. Rakovich and J.F. DoneganBiological Applications of Cadmium Telluride Semiconductor Quantum Dots, A. Le Cign

  14. Elektrokemisk fjernelse af cadmium fra bioasker

    DEFF Research Database (Denmark)

    Pedersen, Anne Juul; Ottosen, Lisbeth M.; Simonsen, Peter;

    Posteren viser resultater fra elektrokemiske rensningsforsøg på bioasker udført i forbindelse med PSO projekt 5205 "Elektrokemisk fjernelse af cadmium fra bioasker i pilotskala og vurdering af mulighederne for nyttiggørelse af behandlet aske i beton".......Posteren viser resultater fra elektrokemiske rensningsforsøg på bioasker udført i forbindelse med PSO projekt 5205 "Elektrokemisk fjernelse af cadmium fra bioasker i pilotskala og vurdering af mulighederne for nyttiggørelse af behandlet aske i beton"....

  15. Crystallization Kinetics of Organic–Inorganic Trihalide Perovskites and the Role of the Lead Anion in Crystal Growth

    KAUST Repository

    Moore, David T.

    2015-02-18

    © 2015 American Chemical Society. Methylammonium lead halide perovskite solar cells continue to excite the research community due to their rapidly increasing performance which, in large part, is due to improvements in film morphology. The next step in this progression is control of the crystal morphology which requires a better fundamental understanding of the crystal growth. In this study we use in situ X-ray scattering data to study isothermal transformations of perovskite films derived from chloride, iodide, nitrate, and acetate lead salts. Using established models we determine the activation energy for crystallization and find that it changes as a function of the lead salt. Further analysis enabled determination of the precursor composition and showed that the primary step in perovskite formation is removal of excess organic salt from the precursor. This understanding suggests that careful choice of the lead salt will aid in controlling crystal growth, leading to superior films and better performing solar cells.

  16. Axion Crystals

    CERN Document Server

    Ozaki, Sho

    2016-01-01

    The low-energy effective theories for gapped insulators are classified by three parameters: permittivity $\\epsilon$, permeability $\\mu$, and theta angle $\\theta$. Crystals with periodic $\\epsilon$ are known as photonic crystals. We here study the band structure of photons in a new type of crystals with periodic $\\theta$ (modulo $2\\pi$) in space, which we call the axion crystals. We find that the axion crystals have a number of new properties that the usual photonic crystals do not possess, such as the helicity-dependent photonic band gaps and the nonrelativistic gapless dispersion relation at small momentum. We briefly discuss possible realizations of axion crystals in condensed matter systems as well as high-energy physics.

  17. Reversible radiochromic plate based on polyvinyl alcohol-iodide complex containing silica nanoparticles

    International Nuclear Information System (INIS)

    A radiochromic plate based on a reversible change between iodide and iodine was prepared using a polyvinyl alcohol-iodide complex, silica nanoparticles, and agarose. X-ray (30 kV, 15 mA) irradiation of the plate changed it to a red color, which gradually disappeared and was completely erased within a day after stopping X-ray irradiation. The minimum detection dose was about 0.5 Gy for X-rays and 10 Gy for 137Cs γ-rays. The G-value for the oxidation of I- was estimated to be about 19.6 in a neutral solution and about 20.64 in an acidic solution. (author)

  18. Parametric study on removal efficiency of impregnated activated charcoal and silver zeolite for radioactive methyl iodide

    International Nuclear Information System (INIS)

    The removal efficiency of impregnated activated charcoal and silver zeolite for radioactive methyl iodide is influenced by various parameters such as temperature, relative humidity, face velocity and packing density. This study is to evaluate the dependency of the removal efficiency on each parameter and these combined parameters, quantitatively. Four types of adsorbents, BC-727, AgX, CHC-50 and SS 208C 5KI3, were tested. From experimental data and mass transfer theory, an experimental equation for evaluating the removal efficiency of adsorbents was derived under a series of experiments for radioactive methyl iodine-131. It was concluded that the removal efficiency calculated from the experimental equation agreed well with the experimental value. Effects of experimental specific parameters, such as Pre-flow time, methyl iodide injection time and After-flow time, on the removal efficiency of adsorbent are also described

  19. Iodide Recognition and Sensing in Water by a Halogen-Bonding Ruthenium(II)-Based Rotaxane.

    Science.gov (United States)

    Langton, Matthew J; Marques, Igor; Robinson, Sean W; Félix, Vítor; Beer, Paul D

    2016-01-01

    The synthesis and anion-recognition properties of the first halogen-bonding rotaxane host to sense anions in water is described. The rotaxane features a halogen-bonding axle component, which is stoppered with water-solubilizing permethylated β-cyclodextrin motifs, and a luminescent tris(bipyridine)ruthenium(II)-based macrocycle component. (1) H NMR anion-binding titrations in D2 O reveal the halogen-bonding rotaxane to bind iodide with high affinity and with selectively over the smaller halide anions and sulfate. The binding affinity trend was explained through molecular dynamics simulations and free-energy calculations. Photo-physical investigations demonstrate the ability of the interlocked halogen-bonding host to sense iodide in water, through enhancement of the macrocycle component's Ru(II) metal-ligand charge transfer (MLCT) emission. PMID:26626866

  20. Induction of iodide uptake in transformed thyrocytes: a compound screening in cell lines

    Energy Technology Data Exchange (ETDEWEB)

    Froehlich, Eleonore [University of Tuebingen, Department of Endocrinology, Metabolism, Nephrology and Clinical Chemistry, Internal Medicine, Tuebingen (Germany); Brossart, Peter [University of Tuebingen, Department of Haematology, Oncology, Immunology and Rheumatology, Internal Medicine, Tuebingen (Germany); Wahl, Richard [University of Tuebingen, Department of Endocrinology, Metabolism, Nephrology and Clinical Chemistry, Internal Medicine, Tuebingen (Germany); Department IV, Internal Medicine, Tuebingen (Germany)

    2009-05-15

    Retinoic acid presently is the most advanced agent able to improve the efficacy of radioiodine therapy in differentiated thyroid carcinoma. In order to identify compounds with higher efficacy a panel of pharmacologically well-characterized compounds with antitumour action in solid cancer cell lines was screened. The effects of the compounds on iodide uptake, cell number, proliferation and apoptosis were evaluated. In general, compounds were more effective in cell lines derived from more aggressive tumours. The effectiveness in terms of number of responsive cell lines and maximal increase in iodide uptake achieved decreased in the order: APHA > valproic acid {approx} sirolimus {approx} arsenic trioxide > retinoic acid {approx} lovastatin > apicidine {approx} azacytidine {approx} retinol {approx} rosiglitazone {approx} bortezomib. We hypothesize that testing of cells from primary tumours or metastases in patients may be a way to identify compounds with optimum therapeutic efficacy for individualized treatment. (orig.)

  1. Gap energy studied by optical transmittance in lead iodide monocrystals grown by Bridgman's Method

    Directory of Open Access Journals (Sweden)

    Veissid N.

    1999-01-01

    Full Text Available The bandgap energy as a function of temperature has been determined for lead iodide. The monocrystal was obtained in a vacuum sealed quartz ampoule inside a vertical furnace by Bridgman's method. The optical transmittance measurement enables to evaluate the values of Eg. By a fitting procedure of Eg as a function of temperature is possible to extract the parameters that govern its behavior. The variation of Eg with temperature was determined as: Eg(T = Eg(0 - aT2/(a + T, with: Eg(0 = (2.435 ± 0.008 eV, a = (8.7 ± 1.3 x 10-4 eV/K and a = (192 ± 90 K. The bandgap energy of lead iodide at room temperature was found to be 2.277 ± 0.007 eV.

  2. Non-isothermal adsorption of radioactive methyl iodide at high temperature

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Byung Seon; Park, Geun Il; Lee, Jung Won; Yoon, Ju Hyeon [KAERI, Taejon (Korea, Republic of); Yang, Ho Yeon [KHNPC, Taejon (Korea, Republic of); Ryu, Seung Kon [Chungnam National Univ., Taejon (Korea, Republic of)

    2003-07-01

    Although activated carbon has been successfully used in nuclear power plants, it cannot be considered as a primary adsorbent in a high temperature system, because of its low ignition temperature and its adverse reaction with nitrogen oxide. Therefore, activated carbon is virtually ruled out for high temperature operating systems. The adsorption and dynamic characteristics of gaseous methyl iodide for silver ion-exchanged zeolites at high temperatures up to 400 .deg. C was evaluated. In this study a simple nonisothermal and axially dispersed plug-flow was adopted to simulate the experimental breakthrough curves. The Langmuir-Freundlich isotherm model was used to represent the equilibrium relationship, and the linear driving force (LDF) approximation was used to represent the article uptake. From the viewpoint of silver utilization for the removal of methyl iodide, both the optimal operating temperature and the effective silver ion-exchange level were also determined.

  3. Performance of non-coconut base adsorbers in removal of iodine and organic iodides

    International Nuclear Information System (INIS)

    Systems for the removal of radioactive iodine and organic iodides have used impregnated coconut shell activated carbons almost exclusively. Coconut shell carbons have some disadvantages: their geographical origin determines their trace chemical content; pore structures and impregnant effectiveness are highly dependent on activation and impregnation techniques. The authors report laboratory performance of a group of iodine-organic iodide adsorbers using bases other than coconut shell carbon. These have been evaluated in conformity with USAEC Regulatory Guide 1.52 and RDT M16 1T. Performance with regard to 131I2 and CH3131I penetration and high-temperature elution have equaled or exceeded both the requirements of Guide 1.52 and results on typical coconut-shell carbons. Some performance outside Guide 1.52 ranges is included. Experimental problems in simulated LOCA testing are discussed. (U.S.)

  4. Heck Arylation of Acrylonitrile with Aryl Iodides Catalyzed by a Silica-bound Arsine Palladium(0) Complex

    Institute of Scientific and Technical Information of China (English)

    Ming Zhong CAI; Hong ZHAO; Rong Li ZHANG

    2005-01-01

    Acrylonitrile reacts with aryl iodides in the presence of tri-n-butylamine and a catalytic amount of a silica-bound arsine palladium(0) complex to afford stereoselectively (E)-cinnamonitriles in high yields.

  5. A mercuric ensemble based on a cycloruthenated complex as a visual probe for iodide in aqueous solution

    Science.gov (United States)

    Su, Xianlong; Guo, Lieping; Ma, Yajuan; Li, Xianghong

    2016-01-01

    A new water-soluble cycloruthenated complex Ru(bthiq)(dcbpy)2+ (1, Hbthiq = 1-(2-benzo[b]thiophenyl)isoquinoline, dcbpy = 4,4‧-dicarboxylate-2,2‧-bipyridine) was designed and synthesized to form its mercuric ensemble (1-Hg2+) to achieve visual detection of iodide anions. The binding constant of 1-Hg2+ is calculated to be 2.40 × 104 M-1, which is lower than that of HgI2. Therefore, the addition of I- to the aqueous solution of 1-Hg2+lead to significant color changes from yellow to deep-red by the release of 1. The results showed that iodide anions could be easily detected by the naked eyes. The detection limit of iodide anion is calculated as 0.77 μM. In addition, an easily-prepared test strip of 1-Hg2+ was obtained successfully to detect iodide anions.

  6. Cooperative effect of silver in copper-catalyzed trifluoromethylation of aryl iodides using Me3SiCF3

    KAUST Repository

    Weng, Zhiqiang

    2011-06-13

    An effective model of cooperative effect of silver for the coppercatalyzed trifluoromethylation of activated and unactivated aryl iodides to trifluoromethylated arenes using Me3SiCF3 was achieved with a broad substrate scope. © 2011 American Chemical Society.

  7. Synthesis and characterization of the 1:1 adducts of copper(I) halides with bidentate N,N′-bis(benzophenone)-1,2-diiminoethane Schiff base: Crystal structures of [Cu(bz2en)2][CuX2] (X = Br, I) complexes

    NARCIS (Netherlands)

    Kia, Reza; Mirkhani, Valiollah; Harkema, Sybolt; Hummel, van Gerrit J.

    2007-01-01

    1:1 adducts of N,N′-bis(benzophenone)-1,2-diiminoethane (bz2en) with copper(I) chloride, bromide and iodide, [Cu(bz2en)2][CuX2] (X = Cl, Br, and I), have been synthesized and the structures of the solid bromide and iodide adducts were determined by X-ray crystallography from single-crystal data. The

  8. The synthesis of SbSI rodlike crystals with studded pyramids

    Science.gov (United States)

    Yang, Qing; Tang, Kaibin; Wang, Chunrui; Hai, Bin; Shen, Guozhen; An, Changhua; Zhang, Chunjuan; Qian, Yitai

    2001-12-01

    The SbSI rodlike crystals with studded pyramids were synthesized from the reaction among antimony trichloride, thiourea, and excessive sodium iodide under moderate hydrothermal conditions at 200°C. The final products were characterized by XRD, SEM, XPS, and elemental analysis. The SEM images showed the SbSI rodlike crystals are inserted some octahedrons on the surfaces of the rods. Typically, the structure is 3-4 mm in length, 8-10 μm in diameter for a singular crystal. The size of the pyramids on the surface is about 10 μm in height and the length of hemline is 6-12 μm.

  9. Cadmium exposure and pancreatic cancer in south Louisiana.

    Science.gov (United States)

    Luckett, Brian G; Su, L Joseph; Rood, Jennifer C; Fontham, Elizabeth T H

    2012-01-01

    Cadmium has been hypothesized to be a pancreatic carcinogen. We test the hypothesis that cadmium exposure is a risk factor for pancreatic cancer with a population-based case-control study sampled from a population with persistently high rates of pancreatic cancer (south Louisiana). We tested potential dietary and nondietary sources of cadmium for their association with urinary cadmium concentrations which reflect long-term exposure to cadmium due to the accumulation of cadmium in the kidney cortex. Increasing urinary cadmium concentrations were significantly associated with an increasing risk of pancreatic cancer (2nd quartile OR = 3.34, 3rd = 5.58, 4th = 7.70; test for trend P ≤ 0.0001). Potential sources of cadmium exposure, as documented in the scientific literature, found to be statistically significantly associated with increased risk of pancreatic cancer included working as a plumber, pipefitter or welder (OR = 5.88) and high consumption levels of red meat (4th quartile OR = 6.18) and grains (4th quartile OR = 3.38). Current cigarette smoking, at least 80 pack years of smoking, occupational exposure to cadmium and paints, working in a shipyard, and high consumption of grains were found to be statistically significantly associated with increased concentrations of urinary cadmium. This study provides epidemiologic evidence that cadmium is a potential human pancreatic carcinogen. PMID:23319964

  10. Cadmium Exposure and Pancreatic Cancer in South Louisiana

    Directory of Open Access Journals (Sweden)

    Brian G. Luckett

    2012-01-01

    Full Text Available Cadmium has been hypothesized to be a pancreatic carcinogen. We test the hypothesis that cadmium exposure is a risk factor for pancreatic cancer with a population-based case-control study sampled from a population with persistently high rates of pancreatic cancer (south Louisiana. We tested potential dietary and nondietary sources of cadmium for their association with urinary cadmium concentrations which reflect long-term exposure to cadmium due to the accumulation of cadmium in the kidney cortex. Increasing urinary cadmium concentrations were significantly associated with an increasing risk of pancreatic cancer (2nd quartile OR = 3.34, 3rd = 5.58, 4th = 7.70; test for trend P≤0.0001. Potential sources of cadmium exposure, as documented in the scientific literature, found to be statistically significantly associated with increased risk of pancreatic cancer included working as a plumber, pipefitter or welder (OR = 5.88 and high consumption levels of red meat (4th quartile OR = 6.18 and grains (4th quartile OR = 3.38. Current cigarette smoking, at least 80 pack years of smoking, occupational exposure to cadmium and paints, working in a shipyard, and high consumption of grains were found to be statistically significantly associated with increased concentrations of urinary cadmium. This study provides epidemiologic evidence that cadmium is a potential human pancreatic carcinogen.

  11. Nickel-catalyzed reductive arylation of activated alkynes with aryl iodides

    Science.gov (United States)

    Dorn, Stephanie C. M.; Olsen, Andrew K; Kelemen, Rachel E.; Shrestha, Ruja; Weix, Daniel J.

    2015-01-01

    The direct, regioselective, and stereoselective arylation of activated alkynes with aryl iodides using a nickel catalyst and manganese reductant is described. The reaction conditions are mild (40 °C in MeOH, no acid or base) and an intermediate organomanganese reagent is unlikely. Functional groups tolerated include halides and pseudohalides, free and protected anilines, and a benzyl alcohol. Other activated alkynes including an amide and a ketone also reacted to form arylated products in good yields. PMID:26028781

  12. Use of potassium iodide in Dermatology: updates on an old drug*

    OpenAIRE

    Costa, Rosane Orofino; de Macedo, Priscila Marques; Carvalhal, Aline; Bernardes-Engemann, Andréa Reis

    2013-01-01

    Potassium iodide, as a saturated solution, is a valuable drug in the dermatologist's therapeutic arsenal and is useful for the treatment of different diseases due to its immunomodulatory features. However, its prescription has become increasingly less frequent in dermatology practice. Little knowledge about its exact mechanism of action, lack of interest from the pharmaceutical industry, the advent of new drugs, and the toxicity caused by the use of high doses of the drug are some possible ex...

  13. Study of cadmium electrochemical deposition in sulfate medium

    Energy Technology Data Exchange (ETDEWEB)

    Montiel, T.; Solorza, O.; Sanchez, H.

    2000-03-01

    The cadmium electrochemical deposition process from sulfate medium was studied by means of different electrochemical techniques in both stationary and nonstationary diffusion regimes. The kinetics of the electrochemical reduction of cadmium on solid cadmium electrodes was examined and the kinetic parameters are presented, as well as the diffusion coefficient derived from the different techniques. Temperature has an important effect on the cadmium reduction kinetics, and the activation energy of the process was evaluated. The electrochemical deposition of cadmium is a complex process due to the coexistence of adsorption and nucleation processes; the adsorbed electroactive species appears to be Cd{sup +2}, and a mechanism for cadmium electrodeposition on solid cadmium electrodes is proposed.

  14. Nitro-Grela-type complexes containing iodides - robust and selective catalysts for olefin metathesis under challenging conditions.

    Science.gov (United States)

    Tracz, Andrzej; Matczak, Mateusz; Urbaniak, Katarzyna; Skowerski, Krzysztof

    2015-01-01

    Iodide-containing nitro-Grela-type catalysts have been synthesized and applied to ring closing metathesis (RCM) and cross metathesis (CM) reactions. These new catalysts have exhibited improved efficiency in the transformation of sterically, non-demanding alkenes. Additional steric hindrance in the vicinity of ruthenium related to the presence of iodides ensures enhanced catalyst stability. The benefits are most apparent under challenging conditions, such as very low reaction concentrations, protic solvents or with the occurrence of impurities. PMID:26664602

  15. Peroxide effects of iodide excess on mitochondria in Fischer rat thyroid cell line in the early period

    Institute of Scientific and Technical Information of China (English)

    李敏

    2014-01-01

    Objective To investigate the peroxide effects of iodide excess on mitochondria in Fischer rat thyroid cell line(FRTL)in the early period.Methods After treatment with 0.0 mmol/L(control group)or 0.1 mmol/L potassium iodide(KI)for 2,4 and 24 h,respectively,changes of mitochondrial superoxide formation were assayed by flow cytometry and fluorescence microscopy using mitochondria-targeted hydroethidine(Mito SOX).

  16. Chlorine Dioxide-Iodide-Methyl Acetoacetate Oscillation Reaction Investigated by UV-Vis and Online FTIR Spectrophotometric Method

    OpenAIRE

    Laishun Shi; Xiaomei Wang; Na Li; Jie Liu; Chunying Yan

    2012-01-01

    In order to study the chemical oscillatory behavior and mechanism of a new chlorine dioxide-iodide ion-methyl acetoacetate reaction system, a series of experiments were done by using UV-Vis and online FTIR spectrophotometric method. The initial concentrations of methyl acetoacetate, chlorine dioxide, potassium iodide, and sulfuric acid and the pH value have great influence on the oscillation observed at wavelength of 289 nm. There is a preoscillatory or induction period, and the amplitude and...

  17. Nitro-Grela-type complexes containing iodides – robust and selective catalysts for olefin metathesis under challenging conditions

    Directory of Open Access Journals (Sweden)

    Andrzej Tracz

    2015-10-01

    Full Text Available Iodide-containing nitro-Grela-type catalysts have been synthesized and applied to ring closing metathesis (RCM and cross metathesis (CM reactions. These new catalysts have exhibited improved efficiency in the transformation of sterically, non-demanding alkenes. Additional steric hindrance in the vicinity of ruthenium related to the presence of iodides ensures enhanced catalyst stability. The benefits are most apparent under challenging conditions, such as very low reaction concentrations, protic solvents or with the occurrence of impurities.

  18. Nitro-Grela-type complexes containing iodides – robust and selective catalysts for olefin metathesis under challenging conditions

    Science.gov (United States)

    Tracz, Andrzej; Matczak, Mateusz; Urbaniak, Katarzyna

    2015-01-01

    Summary Iodide-containing nitro-Grela-type catalysts have been synthesized and applied to ring closing metathesis (RCM) and cross metathesis (CM) reactions. These new catalysts have exhibited improved efficiency in the transformation of sterically, non-demanding alkenes. Additional steric hindrance in the vicinity of ruthenium related to the presence of iodides ensures enhanced catalyst stability. The benefits are most apparent under challenging conditions, such as very low reaction concentrations, protic solvents or with the occurrence of impurities. PMID:26664602

  19. Nitro-Grela-type complexes containing iodides - robust and selective catalysts for olefin metathesis under challenging conditions.

    Science.gov (United States)

    Tracz, Andrzej; Matczak, Mateusz; Urbaniak, Katarzyna; Skowerski, Krzysztof

    2015-01-01

    Iodide-containing nitro-Grela-type catalysts have been synthesized and applied to ring closing metathesis (RCM) and cross metathesis (CM) reactions. These new catalysts have exhibited improved efficiency in the transformation of sterically, non-demanding alkenes. Additional steric hindrance in the vicinity of ruthenium related to the presence of iodides ensures enhanced catalyst stability. The benefits are most apparent under challenging conditions, such as very low reaction concentrations, protic solvents or with the occurrence of impurities.

  20. Murine strain differences and the effects of zinc on cadmium concentrations in tissues after acute cadmium exposure

    Energy Technology Data Exchange (ETDEWEB)

    King, L.M. [ARS USDA, Germplasm and Gamete Physiology Lab., Beltsville, MD (United States); Anderson, M.B. [Dept. of Anatomy, Tulane Univ. School of Medicine, New Orleans, LA (United States); Sikka, S.C. [Dept. of Urology, Tulane Univ. School of Medicine, New Orleans, LA (United States); George, W.J. [Dept. of Pharmacology, Tulane Univ. School of Medicine, New Orleans, LA (United States)

    1998-10-01

    The role of strain differences in cadmium tissue distribution was studied using sensitive (129/J) and resistant (A/J) mice. These murine strains have previously been shown to differ in their susceptibility to cadmium-induced testicular toxicity. Cadmium concentration was measured in testis, epididymis, seminal vesicle, liver, and kidney at 24 h after cadmium chloride exposure (4, 10, and 20 {mu}mol/kg CdCl{sub 2}). The 129/J mice exhibited a significant increase in cadmium concentration in testis, epididymis, and seminal vesicle at all cadmium doses used, compared to A/J mice. However, cadmium concentrations in liver and kidney were not different between the strains, at any dose, indicating that cadmium uptake is similar in these organs at 24 h. These murine strains demonstrate similar hepatic and renal cadmium uptake but significantly different cadmium accumulation in the reproductive organs at 24 h. The mechanism of the protective effect of zinc on cadmium toxicity was studied by assessing the impact of zinc acetate (ZnAc) treatment on cadmium concentrations in 129/J mice after 24 h. Zinc pretreatment (250 {mu}mol/kg ZnAc), given 24 h prior to 20 {mu}mol/kg CdCl{sub 2} administration, significantly decreased the amount of cadmium in the testis, epididymis, and seminal vesicle of 129/J mice, and significantly increased the cadmium content of the liver after 24 h. Cadmium levels in the kidney were unaffected at this time. Zinc pretreatment also prevented the cadmium-induced decrease in testicular sperm concentration and epididymal sperm motility seen in 129/J mice. These findings suggest that the differences in the two murine strains may be attributed partly to the differential accumulation of cadmium in murine gonads. This may be caused by strain differences in the specificity of cadmium transport mechanisms. The protective role of zinc in cadmium-induced testicular toxicity in the sensitive strain may be due to an interference in the cadmium uptake by susceptible

  1. Determination of microamounts of potassium in sodium iodide by atomic absorption spectrometry

    International Nuclear Information System (INIS)

    Microdetermination of potassium in sodium iodide was developed by the standard addition method. Twenty grams of sample were dissolved in 50 ml of water in a quartz beaker. To the solution, 30 ml of concentrated hydrochloric acid and 30 ml of 30% hydrogen peroxide were added, and evaporated to dryness. By this process sodium iodide was converted into sodium chloride. The cake thus obtained was dissolved in water and diluted to exactly 200 ml. To 25 ml aliquots of the solution, the standard potassium and cesium chloride solutions were added and diluted to 50 ml with water; the concentration of potassium was 0 -- 1 mg/l and that of cesium 4 mM. These solutions were introduced into an air-propane flame and the absorbances were measured at 769.9 nm. During the conversion reaction, hydrochloric acid was completely decomposed, and remained hydrogen peroxide had no influence for absorbance, and other backgrounds were negligible. The linear calibration curve was obtained in the range 0 -- 2 mg of potassium per liter. Potassium in sodium iodide was determined by this method within the coefficient of variation of +-(20 -- 3)% in the range (1.7 -- 32.5) ppm. (author)

  2. Iodide Sorption to Clays and the Relationship to Surface Charge and Clay Texture - 12356

    International Nuclear Information System (INIS)

    Iodine is assumed to behave conservatively in clay barriers around nuclear waste repositories and in natural sediments. Batch experiments tend to show little to no sorption, while in column experiments iodine is often retarded relative to tritiated water. Current surface complexation theory cannot account for negatively charged ion sorption to a negatively charged clay particle. Surface protonation and iodide sorption to clay minerals were examined using surface titrations and batch sorption experiments with a suite of clay minerals. Surface titrations were completed spanning a range of both pH values and ionic strengths. For reference, similar titrations were performed on pure forms of an Al-O powder. The titration curves were deconvoluted to attain the pKa distribution for each material at each ionic strength. The pKa distribution for the Al-O shows two distinct peaks at 4.8 and 7.5, which are invariant with ionic strength. The pKa distribution of clays was highly variable between the different minerals and as a function of ionic strength. Iodide sorption experiments were completed at high solid:solution ratios to exacerbate sorption properties. Palygorskite and kaolinite had the highest amount of iodide sorption and montmorillonite had the least. (authors)

  3. Study on multiphoton ionization dissociation processes of ethyl iodide at 800 nm laser radiation

    International Nuclear Information System (INIS)

    Multiphoton ionization-dissociation (MPID) process of ethyl iodide are studied at 800 nm femto-second laser, and time-of-flight mass spectrometer of ethyl iodide are obtained. The result of laser power index shows that the parent-ion mainly undergoes the 3 + 3 resonant enhanced multiphoton ionization (REMPI) process. The percentage of part fragment ions to the total ion current and the laser intensity dependence of the molecule are measured. Based on the experiment results, the multiphoton ionization- dissociation mechanism of ethyl iodide is discussed. The conclusion is that most of ion fragments are produced by C2H5I+ dissociation, this is consistent with the parent-ion dissociation staircase. The two possible dissociation channels of parent-ion are analyzed, but the C-I dissociation is the main channel. We also use Gaussian 03 calculated the energy change of the two channels with B3LYP/3-21G basis set, the theoretical results further demonstrated the experiment. (authors)

  4. Radiofrequency induction on sodium/iodide symporter expression of thyroid cancer

    Institute of Scientific and Technical Information of China (English)

    Youxin Tian; Qinjiang Liu; Yaqiong Ni

    2013-01-01

    Objective:The aim of this study was to investigate the ef ects of radiofrequency treatment on sodium/iodide symporter expression of thyroid cancer cells. Methods:In 29 thyroid cancer patients with low or no expression of soda\\iodide symporter, the radio frequency combined 131I therapy was used, the whole-body scintigraphy and serum Ig were detected before and after the radiofrequency treatment. Results:The whole-body scintigraphy showed that 4 cases (4/29) before radiofrequency treatment had positive iodine uptake, 19 cases (19/29) two weeks after radiofrequency treatment had the positive iodine uptake, 12 cases (12/29) four weeks after radiofrequency treatment had the positive iodine uptake. Four weeks after radiofrequency treatment, 5 cases had increased serum Ig levels, 17 cases had decreased serum Ig levels, 7 cases showed no change. 25 cases (25/29) were ef ective, 15 cases (15/29) were cured. Conclusion:The radiofrequency induced the non-expressed the sodium/iodide symporter of thyroid cancer cells regain the iodine intake ability, it improved the clinical ef icacy of 131I therapy in dedif erentiated thyroid cancer.

  5. Toxic impact of bromide and iodide on drinking water disinfected with chlorine or chloramines.

    Science.gov (United States)

    Yang, Yang; Komaki, Yukako; Kimura, Susana Y; Hu, Hong-Ying; Wagner, Elizabeth D; Mariñas, Benito J; Plewa, Michael J

    2014-10-21

    Disinfectants inactivate pathogens in source water; however, they also react with organic matter and bromide/iodide to form disinfection byproducts (DBPs). Although only a few DBP classes have been systematically analyzed for toxicity, iodinated and brominated DBPs tend to be the most toxic. The objectives of this research were (1) to determine if monochloramine (NH2Cl) disinfection generated drinking water with less toxicity than water disinfected with free chlorine (HOCl) and (2) to determine the impact of added bromide and iodide in conjunction with HOCl or NH2Cl disinfection on mammalian cell cytotoxicity and genomic DNA damage induction. Water disinfected with chlorine was less cytotoxic but more genotoxic than water disinfected with chloramine. For both disinfectants, the addition of Br(-) and I(-) increased cytotoxicity and genotoxicity with a greater response observed with NH2Cl disinfection. Both cytotoxicity and genotoxicity were highly correlated with TOBr and TOI. However, toxicity was weakly and inversely correlated with TOCl. Thus, the forcing agents for cytotoxicity and genotoxicity were the generation of brominated and iodinated DBPs rather than the formation of chlorinated DBPs. Disinfection practices need careful consideration especially when using source waters containing elevated bromide and iodide.

  6. In situ investigation of the formation and metastability of formamidinium lead tri-iodide perovskite solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Aguiar, Jeffery A.; Wozny, Sarah; Holesinger, Terry G.; Aoki, Toshihiro; Patel, Maulik K.; Yang, Mengjin; Berry, Joseph J.; Al-Jassim, Mowafak; Zhou, Weilie; Zhu, Kai

    2016-01-01

    Organic-inorganic perovskites have emerged as an important class of next generation solar cells due to their remarkably low cost, band gap, and sub-900 nm absorption onset. Here, we show a series of in situ observations inside electron microscopes and X-ray diffractometers under device-relevant synthesis conditions focused on revealing the crystallization process of the formamidinium lead-triiodide perovskite at the optimum temperature of 175 degrees C. Direct in situ observations of the structure and chemistry over relevant spatial, temporal, and temperature scales enabled identification of key perovskite formation and degradation mechanisms related to grain evolution and interface chemistry. The lead composition was observed to fluctuate at grain boundaries, indicating a mobile lead-containing species, a process found to be partially reversible at a key temperature of 175 degrees C. Using low energy electron microscopy and valence electron energy loss spectroscopy, lead is found to be bonded in the grain interior with iodine in a tetrahedral configuration. At the grain boundaries, the binding energy associated with lead is consequently shifted by nearly 2 eV and a doublet peak is resolved due presumably to a greater degree of hybridization and the potential for several different bonding configurations. At the grain boundaries there is adsorption of hydrogen and OH- ions as a result of residual water vapor trapped as a non-crystalline material during formation. Insights into the relevant formation and decomposition reactions of formamidinium lead iodide at low to high temperatures, observed metastabilities, and relationship with the photovoltaic performance were obtained and used to optimize device processing resulting in conversion efficiencies of up to 17.09% within the stability period of the devices.

  7. Effects of bacteria on cadmium bioaccumulation in the cadmium hyperaccumulator plant Beta vulgaris var. cicla L.

    Science.gov (United States)

    Chen, Su; Chao, Lei; Sun, Lina; Sun, Tieheng

    2013-01-01

    To investigate the effects of two cadmium-tolerant bacteria, Staphylococcus pasteuri (S. pasteuri X1) and Agrobacterium tumefaciens (A. tumefaciens X2), on cadmium uptake by the cadmium hyperaccumulator plant Beta vulgaris var. cicla L., a pot experiment with artificially contaminated soil was conducted. The results demonstrated that both cadmium-tolerant bacteria enhanced the dry weight of Beta vulgaris var. cicla L. The total dry weights of plants in the control CK20, S. pasteuri X1 and A. tumefaciens X2 treatments were 0.85, 1.13, and 1.38 g/pot, respectively. Compared with the control CK20 findings, the total dry weight of plants was increased by 32.8 and 61.1% after inoculation with S. pasteuri X1 and A. tumefaciens X2, respectively, indicating that A. tumefaciens X2 more strongly promoted the growth of Beta vulgaris var. cicla L. than S. pasteuri X1. In addition, inoculation with S. pasteuri X1 and A. tumefaciens X2 significantly (p < 0.05) promoted cadmium uptake by plants and improved the bioaccumulation of cadmium by the plants from the soil. Moreover, the inoculation of S. pasteuri X1 and A. tumefaciens X2 effectively facilitated the transfer of cadmium in the soil from the Fe-Mn oxide and residual fractions to the soluble plus exchangeable and weakly specially adsorbed fractions in the rhizosphere soils of plants. The bacterial enhancement of cadmium phytoavailability might provide a potential and promising method to increase the efficiency of phytoextraction. PMID:23488173

  8. Specific features of the photoconductivity of semi-insulating cadmium telluride

    Energy Technology Data Exchange (ETDEWEB)

    Golubyatnikov, V. A.; Grigor’ev, F. I.; Lysenko, A. P., E-mail: aplysenko@hse.ru; Strogankova, N. I.; Shadov, M. B. [National Research University Higher School of Economics, Moscow Institute of Electronics and Mathematics (Russian Federation); Belov, A. G. [OAO GIREDMET State Research and Design Institute of the Rare-Metal Industry (Russian Federation)

    2014-12-15

    The effect of local illumination providing a high level of free-carrier injection on the conductivity of a sample of semi-insulating cadmium telluride and on the properties of ohmic contacts to the sample is studied. It is found that, irrespective of the illumination region, the contact resistance of ohmic contacts decreases and the concentration of majority carriers in the sample grows in proportion to the illumination intensity. It is shown that inherent heterogeneities in crystals of semi-insulating semiconductors can be studied by scanning with a light probe.

  9. Simple and rapid determination of iodide in table salt by stripping potentiometry at a carbon-paste electrode.

    Science.gov (United States)

    Svancara, Ivan; Ogorevc, Bozidar; Nović, Milko; Vytras, Karel

    2002-04-01

    A simple and rapid procedure, utilising constant-current stripping analysis (CCSA) at a carbon-paste electrode containing tricresyl phosphate as a pasting liquid (TCP-CPE), has been developed for the determination of iodide in table salt. Because of a synergistic accumulation mechanism based on ion-pairing and extraction of iodide in combination with electrolytic pretreatment of the TCP-CPE, the method is selective for iodide and enables direct determination of iodide in samples of table salt containing anti-caking agents such as K(4)[Fe(CN)(6)] (food additive "E 536") or MgO. The iodide content (calculated as KI) can be determined in a concentration range of 2 to 100 mg kg(-1) salt, with a detection limit (S/N=3) of 1 mg kg(-1), and a recovery from 90 to 115%. The proposed method has been used to determine iodide in several types of artificially iodised table salt and in one sample of natural sea salt. The results obtained agreed well with those obtained by use of three independent reference methods (titration, spectrophotometry, and ICP-MS) used to validate the CCSA method, indicating that the developed method is applicable as a routine procedure for rapid testing in salt production process control and in the analysis of marketed table salts.

  10. Urinary cadmium and estimated dietary cadmium in the Women's Health Initiative.

    Science.gov (United States)

    Quraishi, Sabah M; Adams, Scott V; Shafer, Martin; Meliker, Jaymie R; Li, Wenjun; Luo, Juhua; Neuhouser, Marian L; Newcomb, Polly A

    2016-01-01

    Cadmium, a heavy metal dispersed in the environment as a result of industrial and agricultural applications, has been implicated in several human diseases including renal disease, cancers, and compromised bone health. In the general population, the predominant sources of cadmium exposure are tobacco and diet. Urinary cadmium (uCd) reflects long-term exposure and has been frequently used to assess cadmium exposure in epidemiological studies; estimated dietary intake of cadmium (dCd) has also been used in several studies. The validity of dCd in comparison with uCd is unclear. This study aimed to compare dCd, estimated from food frequency questionnaires, to uCd measured in spot urine samples from 1,002 participants of the Women's Health Initiative. Using linear regression, we found that dCd was not statistically significantly associated with uCd (β=0.006, P-value=0.14). When stratified by smoking status, dCd was not significantly associated with uCd both in never smokers (β=0.006, P-value=0.09) and in ever smokers (β=0.003, P-value=0.67). Our results suggest that because of the lack of association between estimated dCd and measured uCd, dietary estimation of cadmium exposure should be used with caution in epidemiologic studies.

  11. Reduction of stimulated sodium iodide symporter expression by estrogen receptor ligands in breast cancer cells

    Energy Technology Data Exchange (ETDEWEB)

    Cheong, Su-Jin; Jang, DooRye; Jeong, Hwan-Jeong; Lim, Seok Tae; Sohn, Myung-Hee [Department of Nuclear Medicine, Cyclotron Research Center, Research Institute of Clinical Medicine, Chonbuk National University Medical School, Jeonju, Jeonbuk 561-756 (Korea, Republic of); Katzenellenbogen, John A., E-mail: jkatzene@illinois.ed [Department of Chemistry, University of Illinois, Urbana, IL 61801 (United States); Kim, Dong Wook, E-mail: kimdw@chonbuk.ac.k [Department of Nuclear Medicine, Cyclotron Research Center, Research Institute of Clinical Medicine, Chonbuk National University Medical School, Jeonju, Jeonbuk 561-756 (Korea, Republic of)

    2011-02-15

    Purpose: The sodium iodide symporter (NIS) mediates active iodide uptake in lactating breast tissue, and when its levels are enhanced by all-trans retinoic acid (atRA), NIS has been proposed as a target for the imaging and radiotherapy of breast cancer. Importantly, the estrogen receptor {alpha} (ER{alpha}) is an important regulator of atRA induced NIS gene expression in breast cancer cells. In this study, we investigated the effect of an ER agonist (17{beta}-estradiol, E{sub 2}) or antagonist [trans-hydroxytamoxifen (TOT) or raloxifene (RAL)] treatment on the regulation of NIS gene expression and iodide uptake in an ER{alpha}-positive breast cancer (MCF-7) model. Methods: NIS functional activity was measured in vitro by {sup 125}I uptake assay after incubation with E{sub 2} (from 10{sup -15} to 10{sup -5} M), TOT (from 5x10{sup -8} to 5x10{sup -6} M), or RAL (from 5x10{sup -8} to 5x10{sup -6} M) in the presence or absence of atRA (10{sup -7} M). Under the same conditions, NIS mRNA expression was examined by reverse transcriptase polymerase chain reaction. Athymic mice with MCF-7 xenograft tumors were treated with atRA alone or atRA together with E{sub 2} to evaluate the change of {sup 125}I uptake in tumor tissues in vivo. Results: In the iodide uptake study in cells, E{sub 2}, TOT, or RAL treatment alone did not stimulate {sup 125}I uptake. However, when iodide uptake was stimulated by atRA, cotreatment with E{sub 2}, TOT or RAL decreased {sup 125}I uptake in a concentration-dependent manner. The hormone effects on NIS mRNA expression levels in MCF-7 cells were similar. The results of the in vivo biodistribution study showed that {sup 125}I uptake was reduced 50% in tumor tissues of mice treated with atRA/E{sub 2} as compared to tumors treated only with atRA. Conclusion: Our results suggest that combination treatment of atRA and ER ligands could limit the functional activity of the NIS gene induced by atRA, thereby compromising its use as a target for diagnosis

  12. RISK ASSESSMENT FOR CADMIUM IN PHOSPHATE FERTILIZERS

    Science.gov (United States)

    Cadmium induced renal tubular dysfunction occurred where subsistence rice farmers produced their lifetime dietary rice on Zn-mine waste contaminated soils in Japan and other Asian countries. Research has shown that polished rice Cd is greatly increased while grain Zn is not incre...

  13. Field scale behaviour of cadmium in soil.

    NARCIS (Netherlands)

    Boekhold, A.E.

    1992-01-01

    Although total heavy metal contents of soil are often used to express the degree of contamination, they are of little value to judge environmental effects. The main objective of this thesis was to develop and test methodologies with which environmental risks of cadmium pollution of field soils can b

  14. Mobiliteit van cadmium in de bodem

    NARCIS (Netherlands)

    Chardon, W.J.

    1984-01-01

    The adsorption of cadmium by twelve Dutch soils was investigated under widely varying circumstances. The adsorption can be described with the Freundlich equation; the parameters of this equation can be predicted using the properties of the soil (pH, organic carbon and clay content).The adsorption ap

  15. Cadmium isotope variations in the Southern Ocean

    NARCIS (Netherlands)

    Xue, Z.; Rehkämper, M.; Horner, T.J.; Abouchami, W.; Middag, R.; van de Flierd, T.; de Baar, H.J.W.

    2013-01-01

    Cadmium concentrations and isotope compositions were determined for 47 seawater samples from the high nutrient low chlorophyll (HNLC) zone of the Atlantic sector of the Southern Ocean. The samples include 13 surface waters from a transect of the Weddell Gyre and 3 depth profiles from the Weddell Sea

  16. RNA Crystallization

    Science.gov (United States)

    Golden, Barbara L.; Kundrot, Craig E.

    2003-01-01

    RNA molecules may be crystallized using variations of the methods developed for protein crystallography. As the technology has become available to syntheisize and purify RNA molecules in the quantities and with the quality that is required for crystallography, the field of RNA structure has exploded. The first consideration when crystallizing an RNA is the sequence, which may be varied in a rational way to enhance crystallizability or prevent formation of alternate structures. Once a sequence has been designed, the RNA may be synthesized chemically by solid-state synthesis, or it may be produced enzymatically using RNA polymerase and an appropriate DNA template. Purification of milligram quantities of RNA can be accomplished by HPLC or gel electrophoresis. As with proteins, crystallization of RNA is usually accomplished by vapor diffusion techniques. There are several considerations that are either unique to RNA crystallization or more important for RNA crystallization. Techniques for design, synthesis, purification, and crystallization of RNAs will be reviewed here.

  17. Protein Crystallization

    Science.gov (United States)

    Chernov, Alexander A.

    2005-01-01

    Nucleation, growth and perfection of protein crystals will be overviewed along with crystal mechanical properties. The knowledge is based on experiments using optical and force crystals behave similar to inorganic crystals, though with a difference in orders of magnitude in growing parameters. For example, the low incorporation rate of large biomolecules requires up to 100 times larger supersaturation to grow protein, rather than inorganic crystals. Nucleation is often poorly reproducible, partly because of turbulence accompanying the mixing of precipitant with protein solution. Light scattering reveals fluctuations of molecular cluster size, its growth, surface energies and increased clustering as protein ages. Growth most often occurs layer-by-layer resulting in faceted crystals. New molecular layer on crystal face is terminated by a step where molecular incorporation occurs. Quantitative data on the incorporation rate will be discussed. Rounded crystals with molecularly disordered interfaces will be explained. Defects in crystals compromise the x-ray diffraction resolution crucially needed to find the 3D atomic structure of biomolecules. The defects are immobile so that birth defects stay forever. All lattice defects known for inorganics are revealed in protein crystals. Contribution of molecular conformations to lattice disorder is important, but not studied. This contribution may be enhanced by stress field from other defects. Homologous impurities (e.g., dimers, acetylated molecules) are trapped more willingly by a growing crystal than foreign protein impurities. The trapped impurities induce internal stress eliminated in crystals exceeding a critical size (part of mni for ferritin, lysozyme). Lesser impurities are trapped from stagnant, as compared to the flowing, solution. Freezing may induce much more defects unless quickly amorphysizing intracrystalline water.

  18. Computational crystallization.

    Science.gov (United States)

    Altan, Irem; Charbonneau, Patrick; Snell, Edward H

    2016-07-15

    Crystallization is a key step in macromolecular structure determination by crystallography. While a robust theoretical treatment of the process is available, due to the complexity of the system, the experimental process is still largely one of trial and error. In this article, efforts in the field are discussed together with a theoretical underpinning using a solubility phase diagram. Prior knowledge has been used to develop tools that computationally predict the crystallization outcome and define mutational approaches that enhance the likelihood of crystallization. For the most part these tools are based on binary outcomes (crystal or no crystal), and the full information contained in an assembly of crystallization screening experiments is lost. The potential of this additional information is illustrated by examples where new biological knowledge can be obtained and where a target can be sub-categorized to predict which class of reagents provides the crystallization driving force. Computational analysis of crystallization requires complete and correctly formatted data. While massive crystallization screening efforts are under way, the data available from many of these studies are sparse. The potential for this data and the steps needed to realize this potential are discussed.

  19. Computational crystallization.

    Science.gov (United States)

    Altan, Irem; Charbonneau, Patrick; Snell, Edward H

    2016-07-15

    Crystallization is a key step in macromolecular structure determination by crystallography. While a robust theoretical treatment of the process is available, due to the complexity of the system, the experimental process is still largely one of trial and error. In this article, efforts in the field are discussed together with a theoretical underpinning using a solubility phase diagram. Prior knowledge has been used to develop tools that computationally predict the crystallization outcome and define mutational approaches that enhance the likelihood of crystallization. For the most part these tools are based on binary outcomes (crystal or no crystal), and the full information contained in an assembly of crystallization screening experiments is lost. The potential of this additional information is illustrated by examples where new biological knowledge can be obtained and where a target can be sub-categorized to predict which class of reagents provides the crystallization driving force. Computational analysis of crystallization requires complete and correctly formatted data. While massive crystallization screening efforts are under way, the data available from many of these studies are sparse. The potential for this data and the steps needed to realize this potential are discussed. PMID:26792536

  20. Cadmium phytoextraction potential of different Alyssum species

    Energy Technology Data Exchange (ETDEWEB)

    Barzanti, R., E-mail: rbarzanti@supereva.it [Department of Evolutionary Biology, Universita di Firenze, via Micheli 1, 50121 Firenze (Italy); Colzi, I., E-mail: ilariacolzi@hotmail.it [Department of Evolutionary Biology, Universita di Firenze, via Micheli 1, 50121 Firenze (Italy); Arnetoli, M., E-mail: miluscia@gmail.com [Department of Evolutionary Biology, Universita di Firenze, via Micheli 1, 50121 Firenze (Italy); Gallo, A., E-mail: galloalessia@hotmail.com [Department of Evolutionary Biology, Universita di Firenze, via Micheli 1, 50121 Firenze (Italy); Pignattelli, S., E-mail: sara.pignattelli@gmail.com [Department of Evolutionary Biology, Universita di Firenze, via Micheli 1, 50121 Firenze (Italy); Gabbrielli, R., E-mail: gabbrielli@unifi.it [Department of Evolutionary Biology, Universita di Firenze, via Micheli 1, 50121 Firenze (Italy); Gonnelli, C., E-mail: cristina.gonnelli@unifi.it [Department of Evolutionary Biology, Universita di Firenze, via Micheli 1, 50121 Firenze (Italy)

    2011-11-30

    Highlights: Black-Right-Pointing-Pointer The possibility of using serpentine plants for phytoextraction of Cd was investigated. Black-Right-Pointing-Pointer Variation in Cd tolerance, accumulation and translocation in three Alyssum plants with different phenotypes were found. Black-Right-Pointing-Pointer Alyssum montanum showed higher Cd tolerance and accumulation than the Ni hyperaccumulator Alyssum bertolonii. Black-Right-Pointing-Pointer As for the kinetic parameters of the Cd uptake system, A. montanum presented a low apparent K{sub m} value. Black-Right-Pointing-Pointer The V{sub max} values were not significantly different among the plants. - Abstract: This work was planned for providing useful information about the possibility of using serpentine adapted plants for phytoextraction of cadmium, element scarcely represented in such metalliferous environment. To this aim, we investigated variation in cadmium tolerance, accumulation and translocation in three Alyssum plants with different phenotypes: Alyssum bertolonii, that is a serpentine endemic nickel hyperaccumulator, and two populations of Alyssum montanum, one adapted and one not adapted to serpentine soils. Plants were hydroponically cultivated in presence of increasing concentrations of CdSO{sub 4} for two weeks. For the metal concentration used in the experiments, the three different Alyssum populations showed variation in cadmium tolerance, accumulation and content. The serpentine adapted population of A. montanum showed statistically higher cadmium tolerance and accumulation than A. bertolonii and the population of A. montanum not adapted to serpentine soil thus deserving to be investigated for phytoextraction purposes. Furthermore, as for the kinetic parameters of the cadmium uptake system, A. montanum serpentine population presented a low apparent K{sub m} value, suggesting a high affinity for this metal of its uptake system, whereas the V{sub max} values were not significantly different among the

  1. Cadmium and Chrome Concentrations in Human Milk

    Directory of Open Access Journals (Sweden)

    Sima Nazarpour

    2014-04-01

    Full Text Available Introduction: Nutrition of children has the highest priority in any program aimed at children's health care. Milk contaminated with various toxic elements can have adverse effects on children's health. This study aimed to determine the concentration of heavy metals including cadmium(Cd and chromium (Cr of breast feeding women’s milk in Varamin. Methods: This is a cross sectional study. In the present study, chromium and cadmium levels in milk of 100 mothers attending clinics in the city of Varamin were measured in four to eight weeks after delivery, using atomic absorption spectrometry. Results: The mean values (±SD of Cd and Cr in human milk were 5±6.9 μg/ml and 3±2.7 μg/ml respectively. Result of Linear regression showed that cadmium levels were higher in breast milk of people living close to the factory or industrial center. Also, the chromium levels were higher in the breast milk of women in cases of: Smoking by spouses, consumption of imported rice, consumption of mineral water, and living close to the factory or an industrial center. Conclusion: This study showed that the relationship of some factors such as living near a factory or an industrial center, smoking by spouse, the type of consumed rice and water, with the level of cadmium and chromium. Cadmium and chromium levels of breast milk in this study were higher than the levels of these elements mentioned in the reviewed articles and international standard. Because some variables, such as living near a factory or an industrial center, smoking by spouse, the type of consumed rice and water can affect the amount of entering elements in breast milk. Actions can be taken to reduce or eliminate these variables in order to decrease the mentioned elements in human milk.

  2. Hepatoprotective activity of Moringa oleifera against cadmium toxicity in rats

    Directory of Open Access Journals (Sweden)

    Reetu Toppo

    2015-04-01

    Full Text Available Aim: The present investigation has been conducted to evaluate the hepatoprotective activity of Moringa oleifera against cadmium-induced toxicity in rats. Materials and Methods: For this study, 18 Wistar albino rats were taken. Control group, Group I rats were given cadmium chloride @ 200 ppm per kg and Group II rats were treated with M. oleifera extract @ 500 mg/kg along with cadmium chloride @ 200 ppm per kg (daily oral for 28 days. On 29th day, animals were slaughtered and various parameters were determined. Serum biomarkers, oxidative stress parameters, histomorphological examination were carried out with estimation of cadmium concentration in liver tissues. Results: Oral administration of cadmium chloride @ 200 ppm/kg for 28 days resulted in a significant increase in aspartate aminotransferase (AST, alanine transaminase (ALT, alkaline phosphatase (ALP, significant (p≤0.01 increase of lipid peroxidation (LPO and decrease in superoxide dismutase (SOD, and increase in cadmium accumulation in liver. Treatment with M. oleifera @ 500 mg/kg significantly (p<0.01 decreased the elevated ALP, AST, ALT, LPO levels and increase in SOD levels, and as compared to cadmium chloride treated group. However, there was no significant difference in cadmium concentration in liver when compared with cadmium chloride treated group. Conclusion: The study conclude that supplementation of M. oleifera (500 mg/kg, daily oral for 28 days has shown protection against cadmium-induced hepatotoxicity.

  3. Modelling of Cadmium Transport in Soil-Crop System

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    A model for simulating cadmium transport in a soil-plant system was built using a commercial simu lating program named Powersim on the basis of input-output processes happening in the soil-plant system.Convective and dispersive transport processes of cadmium in soil profile are embedded. Simulations on a daily base have been done up to a total simulating time of 250 years. Results show that applications of sewage sludge and fertilizer at the simulated rates would only cause slight cadmium accumulations in each layer of the soil, and cadmium accumulation would be levelling off, reaching an equilibrium concentrations layer by layer downward after certain time. The time scale to reach an equilibrium concentration varies from 10 years for the top three layers to over 250 years for the bottom layers. Plant cadmium uptake would increase from 52 ug m-2 under initial soil cadmium concentrations to 65 μg m-2 under equilibrium soil cadmium concentrations, which would not exceed the maximum allowable cadmium concentration in wheat grains. Main parameters which influence cadmium accumulation and transport in soil are total cadmium input, rainfall, evaporation, plant uptake and soil properties.

  4. Crystallization, X-ray diffraction analysis and SIRAS/molecular-replacenent phasing of three crystal forms of Anabaena sensory rhodopsin transducer

    Energy Technology Data Exchange (ETDEWEB)

    Vogeley, Lutz; Luecke, Hartmut, E-mail: hudel@uci.edu [University of California, Irvine (United States)

    2006-04-01

    Crystals of Anabaena sensory rhodopsin transducer, the transducer for the cyanobacterial photosensor Anabaena sensory rhodopsin, obtained in the space groups P4, C2 and P2{sub 1}2{sub 1}2{sub 1} diffract to 1.8, 2.1 and 2.0 Å, respectively. Phases for these crystal forms were obtained by SIRAS phasing using an iodide quick-soak derivative (P4) and molecular replacement (C2 and P2{sub 1}2{sub 1}2{sub 1}). Anabaena sensory rhodopsin transducer (ASRT) is a 14.7 kDa soluble signaling protein associated with the membrane-embedded light receptor Anabaena sensory rhodopsin (ASR) from Anabaena sp., a freshwater cyanobacterium. Crystals of ASRT were obtained in three different space groups, P4, C2 and P2{sub 1}2{sub 1}2{sub 1}, which diffract to 1.8, 2.1 and 2.0 Å, respectively. Phases for one of these crystal forms (P4) were obtained by SIRAS phasing using an iodide quick-soak derivative and a partial model was built. Phases for the remaining crystal forms were obtained by molecular replacement using the partial model from the P4 crystal form.

  5. Crystal Data

    Science.gov (United States)

    SRD 3 NIST Crystal Data (PC database for purchase)   NIST Crystal Data contains chemical, physical, and crystallographic information useful to characterize more than 237,671 inorganic and organic crystalline materials. The data include the standard cell parameters, cell volume, space group number and symbol, calculated density, chemical formula, chemical name, and classification by chemical type.

  6. Assessment and management of risk to wildlife from cadmium

    International Nuclear Information System (INIS)

    Cadmium, a nonessential heavy metal that comes from natural and anthropogenic sources, is a teratogen, carcinogen, and a possible mutagen. Assessment of potential risk from cadmium requires understanding environmental exposure, mainly from ingestion, although there is some local exposure through inhalation. Chronic exposure is more problematic than acute exposure for wildlife. There is evidence for bioaccumulation, particularly in freshwater organisms, but evidence for biomagnification up the food chain is inconsistent; in some bird studies, cadmium levels were higher in species that are higher on the food chain than those that are lower. Some freshwater and marine invertebrates are more adversely affected by cadmium exposure than are birds and mammals. There is very little experimental laboratory research on the effects of cadmium in amphibians, birds and reptiles, and almost no data from studies of wildlife in nature. Managing the risk from cadmium to wildlife involves assessment (including ecological risk assessment), biomonitoring, setting benchmarks of effects, regulations and enforcement, and source reduction

  7. Study on electrokinetic remediation of cadmium contaminated soils

    Institute of Scientific and Technical Information of China (English)

    SHI Wen-xin; CUI Chong-wei; YU Shui-li; FENG Wei-ming

    2007-01-01

    Kaolinite from a lead-zinc mining district, which was spiked with cadmium, has been treated by electrokinetics to investigate effects of treatment time and applied voltage gradient. The results showed that the increased test duration had induced a higher removal rate of cadmium. Being treated for 7 days, cadmium was removed from kaolinite dramatically. It was also found that higher removal rate happened when a higher voltage gradient was applied and cadmium accumulated near the cathode because pH increased. Increase of pH near the cathode caused accumulation of cadmium. Moreover, it was observed that cation exchange membrane which was placed between kaolinite and cathode could make pH lower than the initial value and avoid the higher pH near the cathode. As a result, the high concentration accumulation of cadmium near the cathode was avoided.

  8. Research and Development of Cadmium Sulphoselenide Red Pigment

    Institute of Scientific and Technical Information of China (English)

    WU Jianfeng; LI Kun; XU Xiaohong; ZHANG Yaxiang; XU Xiaoyang; LAO Xinbin

    2015-01-01

    Cadmium sulphoselenide was synthesized continuous substitution solid solution and the only known pigment to yield bright red color on ceramic decoration. Encapsulated cadmium sulphoselenide pigments could yield abundant hues from yellow to red with high opacity at high temperature. The color generation has a linear function relation with the substitution rate. The encapsulation formation process of zirconium silicate encapsulated cadmium sulphoselenide was shown. Insufifcient encapsulation efifciency and potential hazard to human and environment had limited the industrial application of cadmium sulphoselenide red pigment. Ink-jet printing decoration required ifne size cadmium sulphoselenide red pigment on ceramic decoration. The review mainly focused on the synthesis techniques and industrial application of cadmium sulphoselenide red pigment.

  9. An optically-interrogated microwave-Poynting-vector sensor using cadmium manganese telluride.

    Science.gov (United States)

    Chen, Chia-Chu; Whitaker, John F

    2010-06-01

    A single cadmium-manganese-telluride crystal that exhibits both the Pockels and Faraday effects is used to produce a Poynting-vector sensor for signals in the microwave regime. This multi-birefringent crystal can independently measure either electric or magnetic fields through control of the polarization of the optical probe beam. After obtaining all the relevant electric and magnetic field components, a map of the Poynting vector along a 50-Omega microstrip was experimentally determined without the need for any further transformational calculations. The results demonstrate that this sensor can be used for near-field mapping of the Poynting vector. Utilizing both amplitude and phase information from the fields in the microwave signal, it was confirmed for the case of an open-terminated microstrip that no energy flowed to the load, while for a microstrip with a matched termination, the energy flowed consistently along the transmission line. PMID:20588348

  10. Towards a biochemical and structural characterisation of the sodium-iodide sym-porter (Nis)

    International Nuclear Information System (INIS)

    Iodide is essential for thyroid hormone biosynthesis in mammals, and therefore for the control of cell metabolism and the development of the central nervous system in the foetus and newborns, but is relatively scarce element in the environment. To ensure its accumulation, the thyroid gland has evolved a remarkably efficient system, the sodium-iodide sym-porter (NIS), that was first characterized at the molecular level 10 years ago (1). NIS is an intrinsic protein mainly located in the basolateral membrane of thyroid follicular cells where it actively transports iodide ions using the sodium gradient as a driving force (2,3). In addition, this transporter has been found in lactating mammary gland, stomach, and salivary glands, and its mRNA was detected in brain, ovaries, testis. To date, the physiological role of NIS in these organs is not yet identified (3,4).The capacity of NIS to mediate the accumulation of radioactive iodide has been exploited for many years in the diagnosis of thyroid cancer as well as for the detection and radiotherapy of derived metastases. Moreover, the presence of NIS in some breast tumours and the possibility to express it by targeted gene therapy in tumour cells where it is not naturally present could also widen its medical application (4-7). In case of accidental contamination, NIS would also be responsible for accumulation of radioisotopes in the thyroid and for their transfer to the milk and the newborn, eventually causing thyroid cancers. This has motivated our research program in the perspective of designing novel specific therapeutics. During the last decade, the gene encoding the thyroid NIS has been identified and sequenced in various species including rat, mouse and human (1, 8). It was also demonstrated that the protein expression and activity are highly regulated both at the transcriptional and post-translational levels (3). A preliminary topological mode could be drawn from the protein sequence. It proposes a general

  11. Iodide Sorption to Clays and the Relationship to the Surface Charge Environment

    Science.gov (United States)

    Miller, A. W.; Wang, Y.

    2011-12-01

    In performance assessments of nuclear waste repositories, iodine-129 is often the major contributor to dose at time scales ≥10,000 years. The breakthrough behavior of iodine is determined by the monovalent, anionic nature and the assumed lack of surface reactivity of the iodide ion. This assumption is corroborated by batch sorption data where iodide sorption to clays is typically very small, and only measurable under specific conditions. This result is consistent with charge repulsion arguments due to the fixed negative charge of clays repelling the anionic iodide. However, in compacted column diffusion experiments, iodide is routinely retarded relative to tritium, and is described with Kd values from ≈0.001-2.9ml/g. While small, these values can dramatically change the dose profile in performance assessment calculations. We hypothesize that contributions from the basal plane and edge charge of individual clay particles as well as the physical morphology of the clay particles are contributing to the conflicting behavior. In a series of experiments involving a wide range of clay minerals from the clay bank repository, both surface charge and iodide sorption were examined using surface titrations and batch sorption experiments. The clay minerals studied include: kaolinite, ripidolite, illite, montmorillonite, palygorskite, sepiolite, and an illite/smectite mixed layer clay. Each of these clays was characterized using XRD, and surface titrations in 0.01, 0.1, and 0.5 M NaCl electrolyte. The titrations spanned the pH range from 2.5-10.5 and were automated using an autotitrator. For reference, similar titrations were performed on pure forms of an Al-O powder. The titration curves were interpreted using an inversion method to attain the pKa distribution for each clay and metal oxide at each ionic strength. The pKa distribution for the Al-O shows two distinct peaks at 4.8 and 7.5, which are invariant with ionic strength. The pKa distribution of clays was highly

  12. In search of biomonitors for cadmium: cadmium content of wild Swedish fauna during 1973-1976.

    Science.gov (United States)

    Frank, A

    1986-12-01

    Forty-five species of birds and 22 species of mammals of the terrestrial and aquatic fauna, herbivores as well as carnivores, were investigated during the period 1973-1976 for cadmium-accumulating properties in order to find biomonitors for cadmium in the Swedish environment. The herbivores of the terrestrial fauna, birds as well as mammals, are preferred to carnivores, since they demonstrate generally higher renal Cd levels. The moose (Alces alces), roe deer (Capreolus capreolus) and hare (Lepus europeus and Lepus timidus) were found to be suitable as biomonitors because of their common occurrence and uniform geographical distribution. The eider duck (Somateria mollissima), although a short-distance migrating bird whose diet is composed mainly of mussels and crustaceans, and which lives along a great part of the Swedish coastline, is suggested as a biomonitor of cadmium for the aquatic environment. The accumulation rate of cadmium in the kidneys is rapid. Renal levels of cadmium in the parts per million range are reached 10 weeks after hatching. Juvenile birds should be collected for monitoring purposes before leaving their feeding domains at the end of the summer. PMID:3810147

  13. Oral cadmium exposure of adults in Germany. 1: Cadmium content of foodstuffs and beverages.

    Science.gov (United States)

    Müller, M; Anke, M; Hartmann, E; Illing-Günther, H

    1996-04-01

    The cadmium contents of 94 and 105 foodstuffs bought in six-fold repetition in 1988 and in nine-fold repetition in 1991, respectively were analysed within the framework of a market-basket study. These foodstuffs were typical of German eating habits. Additionally, 170 samples of drinking water were investigated. The cadmium concentrations of the foodstuffs were comparable with results of recent studies carried out in Europe and North America. Fruit, milk and dairy products, sugar and sugar-rich foodstuffs as well as beverages showed mean cadmium contents cakes and pastries as well as farinaceous products were within the range of 20-40 ng/g. The most important bread, cakes and pastries (wheat and rye bread, toasted bread, rolls) contained 25-35 ng/g. A median cadmium concentration of 0.2 micrograms/l was found in the drinking water. As expected, liver and kidneys showed the highest cadmium levels of 73 and 204 ng/g, respectively on average. PMID:8718751

  14. Hepatotoxicity of Cadmium and Roles of Mitigating Agents

    Directory of Open Access Journals (Sweden)

    Elias Adikwu

    2013-12-01

    Full Text Available There are increasing reports on cadmium associated hepatotoxicity, due to these reports this study reviewed relevant literature on cadmium associated hepatotoxicity with emphasis on doses, route of administration, salt forms (cadmium compounds and the roles of mitigating agents. Reports have shown that continuous exposure of the liver to cadmium has led to hepatotoxicity. Humans are generally exposed to cadmium by two main routes, inhalation and ingestion. In this study, evaluation of relevant literature showed that irrespective of route of administration and salt forms cadmium hepatotoxicity is dose and time dependent. Cadmium associated hepatotoxicity manifested through impaired functions of hepatic biomarkers (transaminases, enzymatic and non enzymatic antioxidants. Histopathological damage to liver architecture manifested as swelling of hepatocytes, focal necrosis, hepatocytes degeneration, dilatation of ribosomes, damage of membrane-bounded lysosomes, nuclear pyknosis and cytoplasm vacuolization. Deterioration of mitochondrial cristae, deposition of collagen fibrils, hypertrophy of kuffer cells, congestion in central veins and sinusoids, infiltration of mixed inflammatory cells and peripheral hemorrhage also occurred. Hepatotoxic effect of cadmium was mitigated by Vitamin C, Vitamin E, Manganese (11 Chloride, N-acetylcysteine and Selenium. Extracts of plant origin including Solanum tuberosum, Calycopteris floribunda Hibiscus sabdariffa mitigated cadmium induced hepatotoxicity. Chemical substances of animal origin including honey and camel milk were reported to have ameliorated cadmium induced hepatotoxicity. One of the mechanisms of cadmium induced hepatotoxicity is reported to be associated with the up regulation of reactive oxygen species (oxidative stress which caused oxidative damage to lipid contents of membranes and direct liver injury. Conclusion cadmium is dose and time dependently hepatotoxic irrespective of route of administration

  15. Distribution and leaching of methyl iodide in soil following emulated shank and drip application.

    Science.gov (United States)

    Guo, Mingxin; Zheng, Wei; Papiernik, Sharon K; Yates, Scott R

    2004-01-01

    Methyl iodide (MeI) is a promising alternative to methyl bromide in soil fumigation. The pest-control efficacy and ground water contamination risks of MeI as a fumigant are highly related to its gas-phase distribution and leaching after soil application. In this study, the distribution and leaching of MeI in soil following shank injection and subsurface drip application were investigated. Methyl iodide (200 kg ha(-1)) was directly injected or drip-applied at a 20-cm depth into Arlington sandy loam (coarse-loamy, mixed, thermic Haplic Durixeralfs) columns (12-cm i.d., 70-cm height) tarped with virtually impermeable film. Concentration profiles of MeI in the soil air were monitored for 7 d. Methyl iodide diffused rapidly after soil application, and reached a 70-cm depth within 2 h. Relative to shank injection, drip application inhibited diffusion, resulting in significantly lower concentration profiles in the soil air. Seven days after MeI application, fumigated soil was uncapped, aerated for 7 d, and leached with water. Leaching of MeI was significant from the soil columns under both application methods, with concentrations of >10 mug L(-1) in the early leachate. The leaching was greater following shank injection than drip application, with an overall potential of 33 g ha(-1) for shank injection and 19 g ha(-1) for drip application. Persistent residues of MeI remaining in soils after leaching were 50 to 240 ng kg(-1), and the contents were slightly higher following shank injection than drip application. The results suggest that fumigation with MeI may pose a risk of ground water contamination in vulnerable areas. PMID:15537937

  16. Phase partitioning, retention kinetics, and leaching of fumigant methyl iodide in agricultural soils

    International Nuclear Information System (INIS)

    Although it is not currently being sold in the USA, the recent US registration of the fumigant methyl iodide has led to an increased interest in its environmental fate and transport. Although some work has now considered its volatile emissions from soil, there remains a lack of experimental data regarding its ability to be retained in soil and ultimately become transported with irrigation/rain waters. Using laboratory batch and soil column experiments, we aimed to better understand the phase partitioning of MeI, the ability of soils to retain MeI on the solid phase, and the potential for leaching of MeI and its primary degradation product, iodide, down a soil profile. Results indicated that MeI was retained by the solid phase of soil, being protected from volatilization and degradation, particularly in the presence of elevated organic matter. Retention was greater at lower moisture content, and maximum retention occurred after 56 days of incubation. At higher moisture content, the liquid phase also became important in retaining MeI within soil. Together with low observed KD values (0.10 to 0.57 mL g−1), these data suggest that MeI may be prone to leaching. Indeed, in a steady-state soil column study, initially retained MeI was transported with interstitial water. The MeI degradation product, iodide, was also readily transported in this manner. The data highlight a potentially significant process by which MeI fate and transport within the environment may be impacted. -- Highlights: ► Following fumigation and venting, MeI is retained by soil. ► Soil organic matter status is highly significant in MeI retention. ► Retained MeI is protected from degradation and volatilization. ► Retained MeI can be removed from the solid phase to the liquid phase and leached.

  17. Electrical properties of solid iodo mercurates resulting from the reaction of HgI2 with alcaline iodides

    Science.gov (United States)

    Ponpon, J. P.; Amann, M.

    2005-01-01

    Potassium iodide solutions are currently used during the fabrication process of mercuric iodide based nuclear radiation detectors. However, KI treatment leaves the HgI2 surface covered with a residual compound (namely the potassium tri-iodo mercurate) which has a significant influence on the surface properties and stability of mercuric iodide devices and therefore on the detectors characteristics. Looking for other solutions to etch mercuric iodide, we found it interesting to investigate the electrical properties of the compounds which may form when etching HgI2 in NH4I, NaI, and RbI. For this purpose, solid iodo mercurates with the cations ammonium, sodium, and rubidium, have been prepared by reacting HgI2 with the solutions of interest. Study of the electrical properties of these samples and comparison with those of potassium tri-iodo mercurate ones, especially with respect to humidity, indicates noticeable stability differences in presence of water vapour. This could have interesting consequences on the surface cleaning of mercuric iodide.

  18. Efficient radiation production in a weakly ionized, low-pressure, nonequilibrium gallium-iodide positive column discharge plasma

    Energy Technology Data Exchange (ETDEWEB)

    Smith, David J; Michael, J Darryl; Midha, Vikas; Cotzas, George M; Sommerer, Timothy J [General Electric Research, One Research Circle, Niskayuna, NY 12309 (United States)

    2007-07-07

    Electric-discharge plasmas in gallium-iodide vapours are experimentally found to convert 40% of input electric power into ultraviolet and visible radiation (200-800 nm). The conditions are a weakly ionized positive column consisting of 5-10 Torr argon, and the gallium-iodide vapour is formed by heating condensed gallium-iodide to 100-120 deg. C. The input power density is 50-100 mW cm{sup -3}. The plasma is contained in a sealed silica tube and excited by an external radiofrequency antenna. Computational analysis and plasma diagnostics lead to a quantitative understanding that gallium atoms are formed by electron-impact dissociation of gallium-iodide compounds that evaporate into the plasma volume, and that further electron collisions excite the gallium atoms, which then decay by photon emission. High efficiency is possible only because several photons are emitted per dissociation event, and because nonradiative power channels such as electron-impact elastic heating and vibrational excitation are not dominant. The dissociated species recombine on the wall to reform the species that evaporates. The plasma properties change discontinuously as the molar ratio of iodine to gallium (I/Ga) in the system crosses the values I/Ga = 3 and I/Ga = 2, consistent with the thermodynamic properties of condensed gallium-iodide compounds.

  19. Synergy between iodide ions and mangrove tannins as inhibitors of mild steel corrosion

    OpenAIRE

    Adam, Mohd Ridhwan; Rahim, Afidah Abdul; Shah, Affaizza Mohamad

    2015-01-01

    Context Corrosion of materials is a problem faced by many industries. One of the solutions to this problem is to apply corrosion inhibitors.Aims In this study, the synergy between iodide ions and mangrove tannin extracted from mangrove bark (waste products of the charcoal industry) was tested on the inhibition of corrosion of mild steel in 0.5 M HCl and 0.25 M H2SO4. It was compared with the inhibition provided by mimosa and chestnut tannins.MethodsPotentiodynamic and electrochemical impedanc...

  20. Indirect Complexometric Determination of Mercury Using Potassium Iodide as Selective Masking Agent

    OpenAIRE

    RAO, B. Muralidhara

    1998-01-01

    This paper describes a indirect complexometric method for the determination of mercury in the presence of co-ions, based on the selective masking ability of potassium iodide. To the mixture of mercury (II) and other metal ion solution, EDTA solution was added in excess of the metal ions present. The pH of the solution was adjusted to 5.0-6.0 using solid hexamine (10 \\pm 2 g) and surplus EDTA was titrated with zinc sulfate solution using xylenol orange indicator. An excess of solid potassium i...