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Sample records for agi silver iodide

  1. Transformation of dense AgI into a silver-rich framework iodide using thiophenol as mineralizer

    SciTech Connect

    Zhang, Ren-Chun; Zhang, You-Juan; Yuan, Bai-Qing; Miao, Jun-Peng; Pei, Bao-Hua; Liu, Pan-Pan; Wang, Jun-Jie Zhang, Dao-Jun

    2014-12-15

    A new three-dimensional framework iodide, (DabcoH){sub 2}[(Dabco){sub 2}Ag{sub 14}I{sub 16}] (1), was solvothermal synthesized by transformation of dense AgI using p-methylthiophenol as mineralizer, and characterized by elemental analysis, single-crystal and powder X-ray diffraction, thermogravimetric analysis, differential scanning calorimetry analysis, UV–vis diffuse reflectance spectroscopy and fluorescence spectroscopy. Compound 1 crystallizes in the trigonal space group R-3c, a=13.4452(2) Å, c=63.725(2) Å, V=9976.5(4) Å{sup 3}, Z=6. It features a 3D silver-rich [(Dabco){sub 2}Ag{sub 14}I{sub 16}]{sup 2−} anionic framework built up from corner-sharing of hybrid [(Dabco){sub 2}Ag{sub 14}I{sub 19}]{sup 5−} clusters, with protonated DabcoH{sup +} as counterions residing in the channels. UV–vis reflectance spectroscopy reveals the band gap of 1 is 3.3 eV. Compound 1 exhibits a strong photoluminescent emission band at 567 nm upon excitation at 489 nm. - Graphical abstract: A new 3-D iodoargentate was synthesized by transformation of dense AgI in I{sup −}-deficient system using thiophenol as mineralizer. - Highlights: • We have developed a new method to synthesize iodide using thiophenol as mineralizer. • A new 3D iodide, (DabcoH){sub 2}[(Dabco){sub 2}Ag{sub 14}I{sub 16}], was synthesized by transformation of dense AgI under solvothermal condition. • The compound features a 3D Ag–I framework with highest Ag/I ratio. • Compound 1 is a semiconductor with the band gap of 3.3 eV. • Compound 1 exhibits a strong photoluminescent emission band at 567 nm upon excitation at 489 nm.

  2. Non-toxic silver iodide (AgI) quantum dots sensitized solar cells

    SciTech Connect

    Moosakhani, S.; Sabbagh Alvani, A.A.; Sarabi, A.A.; Sameie, H.; Salimi, R.; Kiani, S.; Ebrahimi, Y.

    2014-12-15

    Highlights: • We have demonstrated AgI sensitized solar cell for the first time. • Obtained mesoporous titania powders possessed small crystallite size, high purity and surface area, and developed mesopores with a narrow pore size distribution. • Photovoltaic measurements revealed the electron injection from AgI to TiO{sub 2}. • The assembled AgI-QD solar cells yielded a power conversion efficiency of 0.64% under one sun illumination. • AgI may be a suitable candidate material for use as a non-toxic sensitizer in QDSSC. - Abstract: The present study reports the performance of a new photosensitizer -AgI quantum dots (QDs)- and mesoporous titania (TiO{sub 2}) nanocrystals synthesized by sol–gel (SG) method for solar cells. Furthermore, the effects of n-heptane on the textural properties of TiO{sub 2} nanocrystals were comprehensively investigated by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), N{sub 2} adsorption–desorption measurements, and UV–vis spectroscopy. TiO{sub 2} powders exhibited an anatase-type mesoporous structure with a high surface area of 89.7 m{sup 2}/g. Afterwards, the QDs were grown on mesoporous TiO{sub 2} surface to fabricate a TiO{sub 2}/AgI electrode by a successive ionic layer adsorption and reaction (SILAR) deposition route. Current–voltage characteristics and electrochemical impedance spectroscopy (EIS) data demonstrated that the injection of photoexcited electrons from AgI QDs into the TiO{sub 2} matrix produces photocurrents. The assembled AgI-QD solar cells yielded a power conversion efficiency of 0.64% and a short-circuit current of 2.13 mA/cm{sup 2} under one sun illumination.

  3. Transformation of dense AgI into a silver-rich framework iodide using thiophenol as mineralizer

    NASA Astrophysics Data System (ADS)

    Zhang, Ren-Chun; Zhang, You-Juan; Yuan, Bai-Qing; Miao, Jun-Peng; Pei, Bao-Hua; Liu, Pan-Pan; Wang, Jun-Jie; Zhang, Dao-Jun

    2014-12-01

    A new three-dimensional framework iodide, (DabcoH)2[(Dabco)2Ag14I16] (1), was solvothermal synthesized by transformation of dense AgI using p-methylthiophenol as mineralizer, and characterized by elemental analysis, single-crystal and powder X-ray diffraction, thermogravimetric analysis, differential scanning calorimetry analysis, UV-vis diffuse reflectance spectroscopy and fluorescence spectroscopy. Compound 1 crystallizes in the trigonal space group R-3c, a=13.4452(2) Å, c=63.725(2) Å, V=9976.5(4) Å3, Z=6. It features a 3D silver-rich [(Dabco)2Ag14I16]2- anionic framework built up from corner-sharing of hybrid [(Dabco)2Ag14I19]5- clusters, with protonated DabcoH+ as counterions residing in the channels. UV-vis reflectance spectroscopy reveals the band gap of 1 is 3.3 eV. Compound 1 exhibits a strong photoluminescent emission band at 567 nm upon excitation at 489 nm.

  4. Aqueous Dissolution of Silver Iodide and Associated Iodine Release Under Reducing Conditions with Sulfide

    SciTech Connect

    Yaohiro Inagaki; Toshitaka Imamura; Kazuya Idemitsu; Tatsumi Arima; Osamu Kato; Hidekazu Asano; Tsutomu Nishimura

    2007-07-01

    Aqueous dissolution tests of silver iodide (AgI) were performed in Na{sub 2}S solutions in order to evaluate, empirically, dissolution of AgI to release iodine under reducing conditions with sulfide. The results indicated that AgI dissolves to release iodine being controlled by mainly precipitation of Ag{sub 2}S. However, the dissolution of AgI can be depressed to proceed, and the thermodynamic equilibrium cannot be attained easily. Solid phase analysis for the reacted AgI suggested that a thin layer of solid silver forming at AgI surface may evolve to be protective against transportation of reactant species, which can lead to the depression in the dissolution of AgI. (authors)

  5. Study on the Preparation and Characteristics of Cellulose/Silver Iodide Nanocomposite Film.

    PubMed

    Lee, Yang Hun; Han, Sung Soo; Kang, Young Ah; Shin, Eun Joo

    2016-06-01

    In this study, the structure and properties of an organic-inorganic composite material prepared from cellulose doped with fine particles of silver iodide (AgI) were examined. The preparation of the composite involved the complexation of cellulose with polyiodide ions, such as I- and 13-, by immersion in iodine/potassium iodide (I2/KI: 0.2, 0.4, 0.6, 0.8, 1.0 M) or potassium iodide (KI: 0.6, 1.2, 1.8, 2.4, 3.0 M) aqueous solutions followed by reaction in a silver nitrate (AgNO3:1.0 M) aqueous solution. These procedures resulted in the in situ formation of fine β-AgI particles within the cellulose matrix. The characteristics and conductivities of prepared cellulose/silver iodide (AgI) nanocomposite films with different I2/KI and KI concentrations were investigated. AgI particle formation and aggregation increased on increasing I2/KI and KI concentrations as determined by SEM. X-ray results showed that KI could penetrate the cellulose crystal region and form AgI particles. The electrical conductivities of nanocomposite films treated with KI were higher than that of I2/KI at < 1.0 M of I2/KI and 3 M of KI, although the weight gain by AgI formation was lower than that of I2/KI. This was also attributed to the formation of smaller AgI particles and crystal defects. Highest electrical conductivity (3.8 x 10(-7) Ω(-1) cm(-1)) was obtained from the cellulose films (1.25 x 10(-11) Ω(-1) cm(-1)) treated with the aqueous solutions of 1.0 M I2/KI and 1.0 M AgNO3. PMID:27427678

  6. REMOVAL OF IODIDE FROM GROUNDWATER USING SILVER CHLORIDE WHITE PAPER

    SciTech Connect

    Johns, M

    2008-11-26

    Releases from the F and H Area Seepage Basins on the Savannah River Site (SRS) have caused groundwater plumes that contain a variety of contaminants. These plumes are releasing contaminants into Fourmile Branch, which is a small tributary of the Savannah River. The metallic contaminant releases to the branch are being controlled by base injection. The base injection targets cationic contaminants and was not intended to reduce the concentration of I-129 in groundwater. SRS and the regulatory agencies believe it is appropriate to investigate remedial alternatives that could reduce the I-129. The Savannah River Site Area Closures Projects (ACP) and the Savannah River National Laboratory (SRNL) are developing an innovative in situ treatment for I-129 using silver chloride (AgCl). The proposed AgCl amendment has a very small particle size and is designed to be injected into the contaminated aquifer to capture I-129. The solubility of AgI is several orders of magnitude lower than the solubility of AgCl. Thus, when I-129 comes in contact with AgCl it forms silver iodide (AgI), which is very stable and essentially insoluble in water. SRNL has been performing bench-scale column tests on the effectiveness of silver chloride to capture iodine in an aqueous solution. These initial tests evaluate silver chloride in four different particle sizes; 4-5 millimeters (standard reagent silver chloride), approximately 1 millimeters (sieved reagent silver chloride), approximately 2 micrometers (ultra fine grind without a grinding agent), and <1 micrometer (ultra fine grind with a grinding agent). The first two experiments with macro-sized particles were proof of principle tests. In these the AgCl was mechanically mixed into a portion of the soil filling the columns. The last two were to test the effectiveness of injecting particles suspended in an aqueous solution--the ability to inject the particles, their retention in the column and their effectiveness at removing dissolved iodide

  7. UV-VIS-NIR spectral optical properties of silver iodide borate glasses

    NASA Astrophysics Data System (ADS)

    Crupi, C.; Di Marco, G.; Torrisi, L.; Branca, C.; Carini, G.; Wanderlingh, U.; D'Angelo, G.

    2014-04-01

    We present a study of optical properties of a series of silver iodide borate glasses(AgI)x(Ag2O·B2O3)1-xby UV-VIS-NIR spectroscopy. The results show an increased absorbance in the whole analysed spectral range when the AgI concentration is augmented. In particular, the enhanced intensity of the wavelength band at 400-500 nm with silver iodine content suggests that this band arises from plasmon-related absorption, describing the formation of silver nanoparticles. With respect to this study, our results could motivate novel target designs consisting of ternary silver boron based bulk glasses for generating resonant absorption of laser light by plasma.

  8. Feasibility study of silver iodide smoke as an atmospheric dispersion tracer for Rocky Flats Plant site, July 1983-December 1984

    SciTech Connect

    Langer, G.

    1986-09-22

    At Rocky Flats Plant, we developed a technique that employs the release of silver iodide (AgI) smoke as a very economical tracer for air dispersion around the Plant. In an emergency, the AgI smoke would trace a contaminant plume over long distances, in real time, to guide emergency response. To test this technique, we experimented with first releasing AgI smoke particles, then tracking them up to 50 km from the Plant by vehicle and aircraft under various typical weather conditions. Able to detect single AgI particles as small as 0.01 ..mu..m in real time, a portable cloud chamber operated on either a pickup truck or a small aircraft. For both procedures, a simple smoke generator operating unattended produced up to 1 x 10/sup 15/ particles/g of AgI. Ground tracking of the smoke (1) showed the influence on dispersion by the midday shift from downslope to upslope flow during stable conditions and (2) provided an interesting case study of a nearby thunderstorm as a transient effect. Aerial tracking during eight flights covered a wide range of meteorological conditions. Convective flow often lofted the smoke completely off the ground before it left the Plant boundary. During inversion conditions, the tracer remained within 100 m of the ground.

  9. In situ fabrication of AgI films on various substrates

    SciTech Connect

    Zheng, Z. Liu, A.R.; Wang, S.M.; Huang, B.J.; Ma, X.M.; Zhao, H.X.; Li, D.P.; Zhang, L.Z.

    2008-08-04

    A facile solution-phase chemical route is developed to directly construct silver iodide (AgI) films/crystals on various substrates including silver foil, silicon wafer and glass, etc. The resulting AgI films were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM) and X-ray photoelectron spectroscopy (XPS). The AgI films with different morphologies can be obtained by controlling the reaction parameters. This method is a simple and fast way for in situ deposition of AgI crystals/films on different substrates. These films may be applied in chemical sensing systems and solid-state batteries as solid electrolytes.

  10. Anti-ice nucleating activity of polyphenol compounds against silver iodide.

    PubMed

    Koyama, Toshie; Inada, Takaaki; Kuwabara, Chikako; Arakawa, Keita; Fujikawa, Seizo

    2014-10-01

    Freeze-avoiding organisms survive sub-zero temperatures without freezing in several ways, such as removal of ice nucleating agents (INAs), production of polyols, and dehydration. Another way is production of anti-ice nucleating agents (anti-INAs), such as has been reported for several antifreeze proteins (AFPs) and polyphenols, that inhibit ice nucleation by inactivating INAs. In this study, the anti-ice nucleating activity of five polyphenol compounds, including flavonoid and tannin compounds of both biological and synthetic origin, against silver iodide (AgI) was examined by measuring the ice nucleation temperature in emulsified polyphenol solutions containing AgI particles. The emulsified solutions eliminated the influence of contamination by unidentified INAs, thus enabling examination of the anti-ice nucleating activity of the polyphenols against AgI alone. Results showed that all five polyphenol compounds used here have anti-ice nucleating activities that are unique compared with other known anti-INAs, such as fish AFPs (type I and III) and synthetic polymers (poly(vinyl alcohol), poly(vinylpyrrolidone) and poly(ethylene glycol)). All five polyphenols completely inactivated the ice nucleating activity of AgI even at relatively low temperatures, and the first ice nucleation event was observed at temperatures between -14.1 and -19.4°C, compared with between -8.6 and -11.8°C for the fish AFPs and three synthetic polymers. These anti-ice nucleating activities of the polyphenols at such low temperatures are promising properties for practical applications where freezing should be prevented. PMID:25086201

  11. Development of silica-coated silver iodide nanoparticles and their biodistribution.

    PubMed

    Sakurai, Yu; Tada, Hiroshi; Gonda, Kohsuke; Takeda, Motohiro; Cong, Liman; Amari, Masakazu; Kobayashi, Yoshio; Watanabe, Mika; Ishida, Takanori; Ohuchi, Noriaki

    2012-01-01

    Nanomaterials have great potential in the field of medicine and have been studied extensively. In a previous study, we addressed the potential of silver iodide (AgI) as X-ray contrast media, because it possessed high imaging ability in the measurement by X-ray computed tomography (X-CT) in vitro, and its surface can be modified with many functional groups. We developed the method of silica coating to make AgI nanoparticles more stable and uniform in size. However, the safety and metabolism of nanoparticles in vivo remains to be determined. The objective of the present study was to evaluate the in vivo biodistribution of silica-coated AgI nanoparticles (SAgINPs). X-CT, transmission electron microscopy (TEM), and inductively coupled plasma atomic emission spectrometry (ICP-AES) were performed prior to and at intervals following the intravenous administration of SAgINPs to rats and rabbits. ICP-AES is a spectral technique that can determine the presence and concentrations of metal samples. The X-CT study showed long-period enhancement in the liver and spleen, but not in the bladder of rats. The TEM study demonstrated that SAgINPs were found in hepatocytes. Using ICP-AES, Ag was detected in the bile juice of rabbits, but not found in the urine of these animals, suggesting that SAgINPs are excreted via the liver. This study shows the quantitative biodistribution of silica-coated nanoparticles for the first time, indicating that our silica coating technique is useful for development of nanoparticles with hepatic excretion. In conclusion, the SAgINPs may provide X-ray contrast media with high imaging ability and biocompatibility. PMID:23132228

  12. Application of a new coordination compound for the preparation of AgI nanoparticles

    SciTech Connect

    Mohandes, Fatemeh; Salavati-Niasari, Masoud

    2013-10-15

    Graphical abstract: Silver iodide nanoparticles have been sonochemically synthesized by using silver salicylate complex, [Ag(HSal)], as silver precursor. A series of control experiments were carried out to investigate the effects of solvent, surfactant concentration, sonication time and temperature on the morphology of AgI nanostructures. - Highlights: • Silver salicylate as a new precursor was applied to fabricate γ-AgI nanoparticles. • To further decrease the particle size of AgI, SDS was used as surfactant. • The effect of preparation parameters on the particle size of AgI was investigated. - Abstract: AgI nanoparticles have been sonochemically synthesized by using silver salicylate, [Ag(HSal)], as silver precursor. To investigate the effects of solvent, surfactant concentration, sonication time and temperature on the morphology of AgI nanostructures, several experiments were carried out. The products were characterized by SEM, TEM, XRD, TGA/DTA, UV–vis, and FT-IR. Based on the experimental findings in this research, it was found that the size of AgI nanoparticles was dramatically dependent on the silver precursor, sonochemical irradiation, and surfactant concentration. Sodium dodecyl sulfate (SDS) was applied as surfactant. When the concentration of SDS was 0.055 mM, very uniform sphere-like AgI nanoparticles with grain size of about 25–30 nm were obtained. These results indicated that the high concentration of SDS could prevent the aggregation between colloidal nanoparticles due to its steric hindrance effect.

  13. New solid electrolytes: substituted organic ammonium silver iodides

    SciTech Connect

    Ferraro, J.R.; Walling, P.L.; Sherren, A.T.

    1980-01-01

    Several new solid electrolytes were synthesized from the reaction of substituted organic ammonium hydroiodides (pyridinium and quinolinium type) and varying quantities of silver iodide. The inductive effects of nucleophilic and electrophilic substitution on the pyridinium or quinolinium ring, as well as substituent position on the ionic conductivity, were determined. Pressure and thermal studies were undertaken to determine if new nonambient conductive phases existed. 39 references, 4 figures, 2 tables.

  14. Note: Heterogeneous ice nucleation on silver-iodide-like surfaces

    NASA Astrophysics Data System (ADS)

    Fraux, Guillaume; Doye, Jonathan P. K.

    2014-12-01

    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+ terminated 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+ terminated face to give a well-ordered hexagonal ice-like bilayer that then acts as a template for further ice growth.

  15. Freezing efficiency of Silver Iodide, ATD and Kaolinite in the contact freezing mode

    NASA Astrophysics Data System (ADS)

    Nagare, Baban; Marcolli, Claudia; Stetzer, Olaf; Lohmann, Ulrike

    2014-05-01

    The importance of heterogeneous ice nucleation via contact freezing is one of the open questions in the atmospheric science community. In our laboratory, we built the Collision Nucleation CHamber (CLINCH) (Ladino et al. 2011) in which falling cloud droplets can collide with aerosol particles. In this study, contact freezing experiments are conducted to investigate the ice nucleation ability of silver iodide (AgI), kaolinite and Arizona Test Dust (ATD). Silver iodide has been known for its ice nucleation ability since 1940s (Vonnegut 1947) while kaolinite is a clay mineral and known to be a moderate ice nucleus. ATD is a commercial dust sample used by many groups to compare different setups. In CLINCH, size selected aerosol particles collide with water droplets of 80 µm diameter. With the extension in chamber length it is possible to vary the interaction time of ice nuclei and the droplets. Our experiments are performed between -10 to -36 ºC for various concentrations of ice nuclei and different interaction times. The frozen fraction of the droplets is determined using the custom-made depolarization detector IODE (Nicolet et al., 2010). Depolarization of linearly polarized incident laser light is used to determine the ratio of frozen droplets to all droplets. Frozen fractions of the three particle types with different residence times from CLINCH will be presented in this study. The number of collisions between a single droplet and several aerosol particles can be calculated by accounting for the theoretical collision efficiency at the experimental conditions in order to obtain the freezing efficiency (frozen fraction/number of collisions). Nucleation efficiency is compared with other contact freezing studies and with immersion freezing

  16. Glass-crystal transition in silver-iodide-doped silver selenomolybdate glasses

    NASA Astrophysics Data System (ADS)

    Deb, B.; Ghosh, A.

    2013-12-01

    In this paper, we have studied the isothermal and non-isothermal glass-crystal transition in AgI-doped silver selenomolybdate glasses using differential scanning calorimetry. We have observed a strong dependence of AgI on the glass-crystal transition of these glasses. The activation energy for the crystallization and the dimensionality of the crystal growth for the isothermal and non-isothermal crystallization processes have been determined. The dimensionality of the crystal growth depends strongly on the AgI content and intriguingly shows different behavior when compared for isothermal and non-isothermal cases. For the present glass system the John-Mehl-Avrami model describes well the isothermal crystallization kinetics, while the Sestak-Berggren model is more suitable to describe the non-isothermal crystallization kinetics for glass-crystal transformation.

  17. Pressure induced ionic-superionic transition in silver iodide at ambient temperature

    NASA Astrophysics Data System (ADS)

    Han, Y. H.; Wang, H. B.; Troyan, I. A.; Gao, C. X.; Eremets, M. I.

    2014-01-01

    Silver iodide (AgI-V) is an archetypical ionic compound for studying the formation mechanism of a superionic state. Previous studies have proven that superionic AgI with high ionic conductivity greater than 0.1 Ω-1cm-1 could only be obtained at high temperatures. We show in this paper that high pressure could also induce the superionic state in AgI even at ambient temperature. Using electrochemical impedance spectroscopy, we investigated Ag+ ions diffusing in rock-salt structured AgI-III and KOH-type AgI-V under high pressures and directly observed the superionic state in AgI-V. The diffusion coefficient of AgI-V is ˜3.4 × 10-4-8.6 × 10-4 cm2/s in the investigated pressure range of 12-17 GPa, comparable with those of superionic α-AgI and AgI-III'. By analyzing the half infinite length Warburg diffusion process, two parameters α and β, which closely relate to the disordered state of Ag+ ions, have been determined and it was suggested that Ag+ ions in AgI-V become disordered. The ionic conductivity of AgI-V is three orders of magnitude higher than that of AgI-III, and has reached around 0.1 Ω-1cm-1. Evidence for all three, the diffusion coefficient, α and β, and conductivity have proven that AgI-V is a superionic conductor at ambient temperature.

  18. Pressure induced ionic-superionic transition in silver iodide at ambient temperature.

    PubMed

    Han, Y H; Wang, H B; Troyan, I A; Gao, C X; Eremets, M I

    2014-01-28

    Silver iodide (AgI-V) is an archetypical ionic compound for studying the formation mechanism of a superionic state. Previous studies have proven that superionic AgI with high ionic conductivity greater than 0.1 Ω(-1)cm(-1) could only be obtained at high temperatures. We show in this paper that high pressure could also induce the superionic state in AgI even at ambient temperature. Using electrochemical impedance spectroscopy, we investigated Ag(+) ions diffusing in rock-salt structured AgI-III and KOH-type AgI-V under high pressures and directly observed the superionic state in AgI-V. The diffusion coefficient of AgI-V is ∼3.4 × 10(-4)-8.6 × 10(-4) cm(2)/s in the investigated pressure range of 12-17 GPa, comparable with those of superionic α-AgI and AgI-III'. By analyzing the half infinite length Warburg diffusion process, two parameters α and β, which closely relate to the disordered state of Ag(+) ions, have been determined and it was suggested that Ag(+) ions in AgI-V become disordered. The ionic conductivity of AgI-V is three orders of magnitude higher than that of AgI-III, and has reached around 0.1 Ω(-1)cm(-1). Evidence for all three, the diffusion coefficient, α and β, and conductivity have proven that AgI-V is a superionic conductor at ambient temperature. PMID:25669568

  19. Kinetics and mechanism of reaction between silver molybdate and mercuric iodide in solid state

    SciTech Connect

    Beg, M.A.; Rafiuddin

    1987-05-01

    The kinetics and the mechanism of the reaction between silver molybdate and mercuric iodide were studied in the solid state by X-ray, chemical analysis, and electrical conductivity measurements. This is a multistep reaction where Ag/sub 2/HgI/sub 4/ is formed as an intermediate. In an equimolar mixture of Ag/sub 2/MoO/sub 4/ and HgI/sub 2/, AgI an HgMoO/sub 4/ are formed, whereas in a 1:2 molar mixture Ag/sub 2/HgI/sub 4/ and HgMoO/sub 4/ are formed. The data for lateral diffusion best fit the equation X/sup n/ = kt, where X is the product thickness, t is time, and k and n are constants. This is a multistep solid state ionic reaction initiated by the diffusion of HgI/sub 2/ molecules as such and not through counterdiffusion of cations.

  20. Silver Iodide-Chitosan Nanotag Induced Biocatalytic Precipitation for Self-Enhanced Ultrasensitive Photocathodic Immunosensor.

    PubMed

    Gong, Lingshan; Dai, Hong; Zhang, Shupei; Lin, Yanyu

    2016-06-01

    In this work, we first exposed that the application of p-type semiconductor, silver iodide-chitosan nanoparticle (SICNP), acted as peroxidase mimetic to catalyze the bioprecipitation reaction for signal-amplification photocathodic immunosensing of human interleukin-6 (IL-6). After immobilization of captured antibody onto a polyethylenimine-functionalized carbon nitride (CN) matrix, SICNPs as photoactive tags and peroxidase mimetics were labeled on secondary antibodies, which were subsequently introduced onto the sensing interface to construct sandwich immunoassay platform through antigen-antibody specific recognition. Due to the matched energy levels between CN and AgI, the photocurrent intensity and photostability of SICNP were dramatically improved with rapid separation and transportation of photogenerated carriers. Moreover, the insoluble product in effective biocatalytic precipitation reaction served as electron acceptor to scavenge the photoexcited electron, leading to great amplification of the photocurrent signal of SICNP again. With the help of multiamplification processes, this photocathodic immunosensor presented a turn-on photoelectrochemical performance for IL-6, which showed wide linear dynamic range from 10(-6) to 10 pg/mL with the ultralow detection limit of 0.737 ag/mL. This work also performed the promising application of SICNP in developing an ultrasensitive, cost-effective, and enzyme-free photocathodic immunosensor for biomarkers. PMID:27180822

  1. A reagentless DNA-based electrochemical silver(I) sensor for real time detection of Ag(I) - the effect of probe sequence and orientation on sensor response.

    PubMed

    Wu, Yao; Lai, Rebecca Y

    2016-06-01

    Ag(I) is known to interact with cytosine (C) via the formation C-Ag(I)-C complexes. The authors have utilized this concept to design six electrochemical Ag(I) sensors using C-rich DNA probes. Alternating current voltammetry and cyclic voltammetry were used to analyze the sensors. The results show that the dual-probe sensors that require the use of both 5'- and 3'-thiolated DNA probes are not suitable for this application, the differences in probe orientation impedes formation of C-Ag(I)-C complexes. Sensors fabricated with DNA probes containing both thymine (T) and C, independent of the location of the alkanethiol linker, do not response to Ag(I) either; T-T mismatches destabilize the duplex even in the presence of Ag(I). However, sensors fabricated with DNA probes containing both adenine (A) and C are ideal for this application, owing to the formation of C-Ag(I)-C complexes, as well as other lesser known interactions between A and Ag(I). Both sensors are sensitive, specific and selective enough to be used in 50% human saliva. They can also be used to detect silver sulfadiazine, a commonly prescribed antimicrobial drug. With further optimization, this sensing strategy may offer a promising approach for detection of Ag(I) in environmental and clinical samples. PMID:26901685

  2. Assessing Pistia stratiotes for phytoremediation of silver nanoparticles and Ag(I) contaminated waters.

    PubMed

    Hanks, Nicole A; Caruso, Joseph A; Zhang, Peng

    2015-12-01

    To study the phytoremediation capabilities of Pistia stratiotes in silver nanoparticle (AgNP) and silver ion contaminated wastewaters, individual plants were grown in media spiked with different concentrations of silver nanoparticle and silver ions (0.02, 0.2, and 2 mg L(-1)). Control experiments were carried out at the same time for comparison purposes. Visual changes in the plants were also recorded periodically during each experiment. Total silver concentrations were monitored in the media before, during, and at the termination of the experiments. In addition, analysis of total silver in plant root and leaf samples after termination were carried out to determine the effect of the different media concentrations. The results showed that P. stratiotes can survive in AgNP and ions under 0.02 mg L(-1) and contaminants are retained within the plant. The use of P. stratiotes as a phytoremediator shows potential in removing heavy metal nanoparticles and is competitive in its removal of the ion counterpart. Even higher concentrations of silver, regardless of form, can be reduced to lower levels than the World Health Organization's maximum contamination limit. PMID:26342265

  3. Millimeter Wave Absorption Bands of Silver/copper Iodides-Phosphate Glasses

    NASA Astrophysics Data System (ADS)

    Awano, Teruyoshi; Takahashi, Toshiharu

    2013-07-01

    Millimeter wave absorption spectra of silver halides doped silver phosphate glasses were measured using an intense coherent transition radiation. Two bands were observed at 8.4cm-1 and 6.3cm-1 in AgI doped AgPO3 glass and 8.7cm-1 and 6.1cm-1 in AgBr doped one. Small difference of peak positions between these glasses suggests that these absorption bands are concerned with a large number of silver ions in dopant molecules. Cu+ conducting glasses

  4. Rapid chromatographic separation of dissoluble Ag(I) and silver-containing nanoparticles of 1-100 nanometer in antibacterial products and environmental waters.

    PubMed

    Zhou, Xiao-Xia; Liu, Rui; Liu, Jing-Fu

    2014-12-16

    Sensitive and rapid methods for speciation analysis of nanoparticulate Ag (NAg) and Ag(I) in complex matrices are urgently needed for understanding the environmental effects and biological toxicity of silver nanoparticles (AgNPs). Herein we report the development of a universal liquid chromatography (LC) method for rapid and high resolution separation of dissoluble Ag(I) from nanoparticles covering the entire range of 1-100 nm in 5 min. By using a 500 Å poresize amino column, and an aqueous mobile phase containing 0.1% (v/v) FL-70 (a surfactant) and 2 mM Na2S2O3 at a flow rate of 0.7 mL/min, all the nanoparticles of various species such as Ag and Ag2S were eluted in one fraction, while dissoluble Ag(I) was eluted as a baseline separated peak. The dissoluble Ag(I) was quantified by the online coupled ICP-MS with a detection limit of 0.019 μg/L. The NAg was quantified by subtracting the dissoluble Ag(I) from the total Ag content, which was determined by ICP-MS after digestion of the sample without LC separation. While the addition of FL-70 and Na2S2O3 into the mobile phase is essential to elute NAg and Ag(I) from the column, the use of 500 Å poresize column is the key to baseline separation of Ag(I) from ∼ 1 nm AgNPs. The feasibility of the proposed method was demonstrated in speciation analysis of dissoluble Ag(I) and NAg in antibacterial products and environmental waters, with very good chromatographic repeatability (relative standard deviations) in both peak area (<2%) and retention time (<0.6%), excellent spiked recoveries in the range of 84.7-102.7% for Ag(I) and 81.3-106.3% for NAg. Our work offers a novel approach to rapid and baseline separation of dissoluble metal ions from their nanoparticulate counterparts covering the whole range of 1-100 nm. PMID:25417798

  5. Electrochemical quantification of iodide ions in synthetic urine using silver nanoparticles: a proof-of-concept.

    PubMed

    Toh, Her Shuang; Tschulik, Kristina; Batchelor-McAuley, Christopher; Compton, Richard G

    2014-08-21

    Typical urinary iodide concentrations range from 0.3 μM to 6.0 μM. The conventional analytical method is based on the Sandell-Kolthoff reaction. It involves the toxic reagent, arsenic acid, and a waiting time of 30 minutes for the iodide ions to reduce the cerium(iv) ions. In the presented work, an alternative fast electrochemical method based on a silver nanoparticle modified electrode is proposed. Cyclic voltammetry was performed with a freshly modified electrode in presence of iodide ions and the voltammetric peaks corresponding to the oxidation of silver to silver iodide and the reverse reaction were recorded. The peak height of the reduction signal of silver iodide was used to plot a calibration line for the iodide ions. Two calibration plots for the iodide ions were obtained, one in 0.1 M sodium nitrate (a chloride-ion free environment to circumvent any interference from the other halides) and another in synthetic urine (which contains 0.2 M KCl). In both of the calibration plots, linear relationships were found between the reduction peak height and the iodide ion concentration of 0.3 μM to 6.0 μM. A slope of 1.46 × 10(-2) A M(-1) and a R(2) value of 0.999 were obtained for the iodide detection in sodium nitrate. For the synthetic urine experiments, a slope of 3.58 × 10(-3) A M(-1) and a R(2) value of 0.942 were measured. A robust iodide sensor with the potential to be developed into a point-of-care system has been validated. PMID:24921222

  6. Electrical properties of silver iodide nanoparticles system embedded into opal porous matrix

    NASA Astrophysics Data System (ADS)

    Lukin, A. E.; Ivanova, E. N.; Pan'kova, S. V.; Solovyev, V. G.; Veisman, V. L.

    2014-12-01

    Opal-based composite with silver iodide nanoparticles (AgI/opal) has been prepared by host-guest technology. Temperature and frequency dependences of electrical conductivity and those of dielectric permittivity of AgI/opal samples were measured. Size effects in this opal-based nanocomposite have been discussed.

  7. The first example of a mixed valence ternary compound of silver with random distribution of Ag(I) and Ag(II) cations.

    PubMed

    Mazej, Zoran; Michałowski, Tomasz; Goreshnik, Evgeny A; Jagličić, Zvonko; Arčon, Iztok; Szydłowska, Jadwiga; Grochala, Wojciech

    2015-06-28

    The reaction between colourless AgSbF6 and sky-blue Ag(SbF6)2 (molar ratio 2 : 1) in gaseous HF at 323 K yields green Ag3(SbF6)4, a new mixed-valence ternary fluoride of silver. Unlike in all other Ag(I)/Ag(II) systems known to date, the Ag(+) and Ag(2+) cations are randomly distributed on a single 12b Wyckoff position at the 4̄ axis of the I4̄3d cell. Each silver forms four short (4 × 2.316(7) Å) and four long (4 × 2.764(6) Å) contacts with the neighbouring fluorine atoms. The valence bond sum analysis suggests that such coordination would correspond to a severely overbonded Ag(I) and strongly underbonded Ag(II). Thorough inspection of thermal ellipsoids of the fluorine atoms closest to Ag centres reveals their unusual shape, indicating that silver atoms must in fact have different local coordination spheres; this is not immediately apparent from the crystal structure due to static disorder of fluorine atoms. The Ag K-edge XANES analysis confirmed that the average oxidation state of silver is indeed close to +1⅓. The optical absorption spectra lack features typical of a metal thus pointing out to the semiconducting nature of Ag3(SbF6)4. Ag3(SbF6)4 is magnetically diluted and paramagnetic (μ(eff) = 1.9 μ(B)) down to 20 K with a very weak temperature independent paramagnetism. Below 20 K weak antiferromagnetism is observed (Θ = -4.1 K). Replacement of Ag(I) with potassium gives K(I)2Ag(II)(SbF6)4 which is isostructural to Ag(I)2Ag(II)(SbF6)4. Ag3(SbF6)4 is a genuine mixed-valence Ag(I)/Ag(II) compound, i.e. Robin and Day Class I system (localized valences), despite Ag(I) and Ag(II) adopting the same crystallographic position. PMID:25815902

  8. Impact of ligand framework on the crystal structures and luminescent properties of Cu(I) and Ag(I) clusters and a coordination polymer derived from thiolate/iodide/dppm ligands.

    PubMed

    Rajput, Gunjan; Yadav, Manoj Kumar; Drew, Michael G B; Singh, Nanhai

    2015-03-16

    New homoleptic hexanuclear Ag(I) and heteroleptic trinuclear Cu(I) clusters and a Cu(I) coordination polymer (CP) of the formulas [Ag6(dtc)6] 1, [Cu3I2(dppm)3(dtc)] 2, and [Cu(ttc)I]∞ 3 (dtc = N-methylbenzyl-N-methyl-thiophenedithiocarbamate; dppm = 1,1-bis(diphenylphosphino)methane; and ttc = dimethyltrithiocarbonate) were synthesized and characterized by elemental analysis, IR, UV-vis, (1)H, (13)C, and (31)P NMR spectroscopies, and their structures were elucidated by X-ray crystallography. The complexes show interesting structures and luminescent properties. Complex 1, which is centrosymmetric, contains four short Ag···Ag interactions at 2 × 2.966(1) and 2 × 3.014(1) Å. There are also several Ag···Ag distances of 3.3-3.4 Å. The molecule shows hexagonal orientation with alternating silver and sulfur atoms of the overlapping Ag3S3 hexagons in the front and rear, along the a axis. Complex 2 is a rare trinuclear cluster complex of Cu(I); the Cu···Cu distances are 2.906(2), 3.551(2), and 3.338(2) Å, the foremost representing a substantial intermetallic contact. The Cu3I2P6S2 core is comprised of three fused distorted hexagonal rings with the I1 atom located at the center participating in all three rings. Complex 3 is an iodide-bridged CP with a "staircase"-like arrangement in which the Cu(I) is tetrahedrally surrounded by a sulfur atom from the ttc ligand and three iodine atoms. Unlike 3, which is nonluminescent, 1 and 2 are strongly luminescent in the solid and solution at room temperature. The time-resolved emission spectra reveal a triexponential decay curve and short mean lifetime characteristic of fluorescence behavior. Diffuse reflectance spectroscopy revealed semiconducting behavior with band gaps of 2.12, 3.01, and 2.18 eV for 1-3, respectively. PMID:25699659

  9. Ice nucleation efficiency of AgI: review and new insights

    NASA Astrophysics Data System (ADS)

    Marcolli, Claudia; Nagare, Baban; Welti, André; Lohmann, Ulrike

    2016-07-01

    AgI is one of the best-investigated ice-nucleating substances. It has relevance for the atmosphere since it is used for glaciogenic cloud seeding. Theoretical and experimental studies over the last 60 years provide a complex picture of silver iodide as an ice-nucleating agent with conflicting and inconsistent results. This review compares experimental ice nucleation studies in order to analyze the factors that influence the ice nucleation ability of AgI. The following picture emerges from this analysis: the ice nucleation ability of AgI seems to be enhanced when the AgI particle is on the surface of a droplet, which is indeed the position that a particle takes when it can freely move in a droplet. The ice nucleation by particles with surfaces exposed to air depends on water adsorption. AgI surfaces seem to be most efficient at nucleating ice when they are exposed to relative humidity at or even above water saturation. For AgI particles that are completely immersed in water, the freezing temperature increases with increasing AgI surface area. Higher threshold freezing temperatures seem to correlate with improved lattice matches as can be seen for AgI-AgCl solid solutions and 3AgI·NH4I·6H2O, which have slightly better lattice matches with ice than AgI and also higher threshold freezing temperatures. However, the effect of a good lattice match is annihilated when the surfaces have charges. Also, the ice nucleation ability seems to decrease during dissolution of AgI particles. This introduces an additional history and time dependence for ice nucleation in cloud chambers with short residence times.

  10. Physical Response of Winter Orographic Clouds over the Sierra Nevada to Airborne Seeding Using Dry Ice or Silver Iodide.

    NASA Astrophysics Data System (ADS)

    Deshler, Terry; Reynolds, David W.; Huggins, Arlen W.

    1990-04-01

    -30 km downwind. Snow crystal concentrations increased, snow crystal habits changed to small rimed particles, and precipitation rates increased by 0.1-1.0 mm h 1. The duration of these effects was short, <10 min per seedline. Changes in ice particle development induced by seeding were similar when seeding with either dry ice or silver iodide. This was found to be the case even at temperatures as warm as 6°C using AgI NH4I NH4ClO4 burned in an acetone solution.

  11. Extranuclear dynamics of 111Ag(→111Cd) doped in AgI nanoparticles

    NASA Astrophysics Data System (ADS)

    Sato, W.; Mizuuchi, R.; Irioka, N.; Komatsuda, S.; Kawata, S.; Taoka, A.; Ohkubo, Y.

    2014-08-01

    Dynamic behavior of the extranuclear field relative to the 111Ag(→111Cd) probe nucleus introduced in a superionic conductor silver iodide (AgI) was investigated by means of the time-differential perturbed angular correlation technique. For poly-N-vinyl-2-pyrrolidone (PVP)-coated AgI nanoparticles, we observed nuclear spin relaxation of the probe at room temperature. This result signifies that Ag+ ions in the polymer-coated sample make hopping motion from site to site at this low temperature. The activation energy for the dynamic motion was successfully estimated to be 46(10) meV. The first atomic-level observation of the temperature-dependent dynamic behavior of Ag+ ions in the polymer-coated AgI is reported.

  12. Silver iodide phosphate glass microsphere resonator integrated on an optical fiber taper.

    PubMed

    Milenko, Karolina; Konidakis, Ioannis; Pissadakis, Stavros

    2016-05-15

    In this Letter, we demonstrate the fabrication and characterization of a robust and functional whispering gallery mode (WGM) resonating system based on a silver iodide phosphate glass microsphere melted on an optical fiber taper. The fabrication process is presented, together with spectral characterization of the device. The effect of the thermal annealing of the soft glass resonator on the whispering gallery modes' excitation and Q-factor is shown and discussed. PMID:27176958

  13. Chitosan finishing nonwoven textiles loaded with silver and iodide for antibacterial wound dressing applications.

    PubMed

    Aubert-Viard, François; Martin, Adeline; Chai, Feng; Neut, Christel; Tabary, Nicolas; Martel, Bernard; Blanchemain, Nicolas

    2015-02-01

    Polyethylene terephtalate (PET) and Polypropylene (PP) textiles are widely used in biomedical application such as wound dressings and implants. The aim of this work was to develop an antibacterial chitosan (CHT) coating activated by silver or by iodine. Chitosan was immobilized onto PET and PP supports using citric acid (CTR) as a crosslinking agent through a pad-dry-cure textile finishing process. Interestingly, depending on the CHT/CTR molar ratio, two different systems were obtained: rich in cationic ammonium groups when the CTR concentration was 1%w/v, and rich in anionic carboxylate groups when the CTR concentration was 10%w/v. As a consequence, such samples could be selectively loaded with iodine and silver nitrate, respectively.Both types of coatings were analyzed using SEM and FTIR, their sorption capacities were evaluated toward iodide/iodate anions (I(-)/IO3(-)) and the silver cations (Ag(+)) were evaluated using elemental analysis. Finally, in vitro evaluations were carried out to evaluate the cytocompatibility on the epithelial cell line. The silver loaded textile reported a stronger antibacterial effect against E.coli (5 log10 reduction) than toward S. aureus (3 log10) while the antibacterial effect of the iodide loaded textiles was limited to 1 log10 to 2 log10 on both strains. PMID:25730424

  14. Surface treatments of silver rods with enhanced iodide adsorption for I-125 brachytherapy seeds.

    PubMed

    Lee, Jin Hee; Choi, Kang Hyuk; Yu, Kook Hyun

    2014-02-01

    This study described an effective method to load (125)I on silver rods for the preparation of a brachytherapy source. We tested various ligands on the silver rod surface to screen the one with the highest adsorption and specific radioactivity. In addition, we investigated the effect of surface etching to increase the adsorption capability followed by the extended surface area. We also found that the use of an oxidant during iodide adsorption can increase the loading significantly. The maximum activity of 137.90MBq/rod (3.7269mCi/rod) was achieved on the etched silver rods with phosphate ligand and hydrogen peroxide as an oxidant. In addition, this is 4.5-fold higher than that of the conventional chloride treatment method. PMID:24393812

  15. Potential risk of acute toxicity induced by AgI cloud seeding on soil and freshwater biota.

    PubMed

    Fajardo, C; Costa, G; Ortiz, L T; Nande, M; Rodríguez-Membibre, M L; Martín, M; Sánchez-Fortún, S

    2016-11-01

    Silver iodide is one of the most common nucleating materials used in cloud seeding. Previous cloud seeding studies have concluded that AgI is not practically bioavailable in the environment but instead remains in soils and sediments such that the free Ag amounts are likely too low to induce a toxicological effect. However, none of these studies has considered the continued use of this practice on the same geographical areas and thus the potential cumulative effect of environmental AgI. The aim of this study is to assess the risk of acute toxicity caused by AgI exposure under laboratory conditions at the concentration expected in the environment after repeated treatments on selected soil and aquatic biota. To achieve the aims, the viability of soil bacteria Bacillus cereus and Pseudomonas stutzeri and the survival of the nematode Caenorhabditis elegans exposed to different silver iodide concentrations have been evaluated. Freshwater green algae Dictyosphaerium chlorelloides and cyanobacteria Microcystis aeruginosa were exposed to silver iodide in culture medium, and their cell viability and photosynthetic activity were evaluated. Additionally, BOD5 exertion and the Microtox® toxicity test were included in the battery of toxicological assays. Both tests exhibited a moderate AgI adverse effect at the highest concentration (12.5µM) tested. However, AgI concentrations below 2.5µM increased BOD5. Although no impact on the growth and survival endpoints in the soil worm C. elegans was recorded after AgI exposures, a moderate decrease in cell viability was found for both of the assessed soil bacterial strains at the studied concentrations. Comparison between the studied species showed that the cyanobacteria were more sensitive than green algae. Exposure to AgI at 0.43μM, the reference value used in monitoring environmental impact, induced a significant decrease in photosynthetic activity that is primarily associated with the respiration (80% inhibition) and, to a lesser

  16. Radioactive iodine capture in silver-containing mordenites through nanoscale silver iodide formation.

    SciTech Connect

    Chapman, K. W.; Chupas, P. J.; Nenoff, T. M.; X-Ray Science Division; SNL

    2010-01-01

    The effective capture and storage of radiological iodine ({sup 129}I) remains a strong concern for safe nuclear waste storage and safe nuclear energy. Silver-containing mordenite (MOR) is a longstanding benchmark for iodine capture; however, the molecular level understanding of this process needed to develop more effective iodine getters has remained elusive. Here we probe the structure and distribution of iodine sorbed by silver-containing MOR using differential pair distribution function analysis. While iodine is distributed between {gamma}-AgI nanoparticles on the zeolite surface and subnanometer {alpha}-AgI clusters within the pores for reduced silver MOR, in the case of unreduced silver-exchanged MOR, iodine is exclusively confined to the pores as subnanometer {alpha}-AgI. Consequently, unreduced silver-containing zeolites may offer a more secure route for radioactive iodine capture, with the potential to more effectively trap the iodine for long-term storage.

  17. A twelve-coordinated iodide in a cuboctahedral silver(I) skeleton.

    PubMed

    Liao, Jian-Hong; Latouche, Camille; Li, Bing; Kahlal, Samia; Saillard, Jean-Yves; Liu, C W

    2014-02-17

    Three new halide-centered octanuclear silver(I) complexes, [Ag8(X){S2P(CH2CH2Ph)2}6](PF6), X = F(-), 1; Cl(-), 2; Br(-), 3; were prepared in the presence of the corresponding halide anions with silver(I) salts and dithiophosphinate ligands. Structure analyses displayed that a Ag8 cubic core can be modulated by the size effect of the central halide; however, an iodide-centered Ag8 cluster was not found under similar reaction conditions. Interestingly, a luminescent dodecanuclear silver(I) cluster, [Ag12(μ12-I)(μ3-I)4{S2P(CH2CH2Ph)2}6](I), 4; was then synthesized. The structure of 4 contains a novel μ12-I at the center of a cuboctahedral silver(I) atom cage, which is further stabilized by four additional μ3-I and six dithiophosphinate ligands. To the best of our knowledge, the μ12-I revealed in 4 is the highest coordination number for a halide ion authenticated by both experimental and computational studies. Previously, the μ12-I was only observed in [PyH][{TpMo(μ3-S)4Cu3}4(μ12-I)]. The synthetic details, spectroscopic studies including multinuclear NMR and ESI-MS, structure elucidations by single crystal X-ray diffraction, and photoluminescence of 4 are reported herein. PMID:24476137

  18. Structure of water in microscopic fractures of a silver iodide crystal

    NASA Astrophysics Data System (ADS)

    Shevkunov, S. V.

    2014-02-01

    The results of a computer simulation of flat fractures with widths of 0.63, 1.25, and 2.5 nm filled with vapor molecules in a silver iodide crystals at 260 K were presented. The two-dimensional gas of molecules adsorbed on the walls was found to be strongly clustered. Before the pore was filled, its walls had been covered with a monomolecular water film with a characteristic hexagonal structure. The perpendicular growth of the film was hindered by the hydrophobicity of its surface; the adsorbed molecules were bonded with the walls by interactions with the ions of the second crystal layer to form a specific orientational molecular order in the region of contact with the wall. On the wall with silver cations, the molecular energy was lower and the entropy higher than on the wall with iodide anions; on the wall with a lower energy, the adsorption started earlier and was more active. In an extremely narrow pore having room for only one molecular layer, the monomolecular film consists of spots held on opposite walls; in each spot, the orientational molecular order is the one characteristic of the wall with which the spot is in contact.

  19. Atomic-level observation of Ag-ion hopping motion in AgI

    NASA Astrophysics Data System (ADS)

    Sato, W.; Komatsuda, S.; Mizuuchi, R.; Irioka, N.; Kawata, S.; Ohkubo, Y.

    2015-04-01

    Applicability of the 111mCd(→111Cd) and 111In(→111Cd) probes to the study of dynamics in polycrystalline silver iodide (AgI) was examined by means of the time-differential perturbed angular correlation technique. It was found that the 111mCd(→111Cd) probe occupies a unique site in γ-AgI and exhibits nuclear relaxation caused by dynamic perturbation arising from Ag + hopping motion in α-AgI; while the residential sites of 111In(→111Cd) vary, suggesting that 111In ions can not settle themselves in a fixed site in the AgI crystal structure. We here demonstrate that 111mCd(→111Cd) can be a potential nucleus to probe the Ag +-ion dynamic motion in α-AgI.

  20. Simulations of Ice Nucleation by Model AgI Disks and Plates.

    PubMed

    Zielke, Stephen A; Bertram, Allan K; Patey, G N

    2016-03-10

    Silver iodide is one of the most effective ice nuclei known. We use molecular dynamics simulations to investigate ice nucleation by AgI disks and plates with radii ranging from 1.15 to 2.99 nm. It is shown that disks and plates in this size range are effective ice nuclei, nucleating bulk ice at temperatures as warm as 14 K below the equilibrium freezing temperature, on simulation time scales (up to a few hundred nanoseconds). Ice nucleated on the Ag exposed surface of AgI disks and plates. Shortly after supercooling an ice cluster forms on the AgI surface. The AgI-stabilized ice cluster fluctuates in size as time progresses, but, once formed, it is constantly present. Eventually, depending on the disk or plate size and the degree of supercooling, a cluster fluctuation achieves critical size, and ice nucleates and rapidly grows to fill the simulation cell. Larger AgI disks and plates support larger ice clusters and hence can nucleate ice at warmer temperatures. This work may be useful for understanding the mechanism of ice nucleation on nanoparticles and active sites of larger atmospheric particles. PMID:26878341

  1. Standard free energy of formation of iron iodide

    NASA Technical Reports Server (NTRS)

    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.

  2. Solid-state superionic stamping with silver iodide-silver metaphosphate glass.

    PubMed

    Jacobs, K E; Hsu, K H; Han, X; Kumar, A; Azeredo, B P; Fang, N X; Ferreira, P M

    2011-10-21

    This paper demonstrates and analyzes the new use of the glassy solid electrolyte AgI-AgPO(3) for direct nanopatterning of thin silver films with feature resolutions of 30 nm. AgI-AgPO(3) has a high room temperature ionic conductivity with Ag( + ) as the mobile ion, leading to silver etch/patterning rates of up to 20 nm s( - 1) at an applied bias of 300 mV. The glass can be melt-processed at temperatures below 200 °C, providing a facile and economical pathway for creating large area stamps, including the 25 mm(2) stamps shown in this study. Further, the glass is sufficiently transparent to permit integration with existing tools such as aligners and imprint tools, enabling high overlay registration accuracy and facilitating insertion into multi-step fabrication recipes. PMID:21934195

  3. Cesium iodide alloys

    DOEpatents

    Kim, H.E.; Moorhead, A.J.

    1992-12-15

    A transparent, strong CsI alloy is described having additions of monovalent iodides. Although the preferred iodide is AgI, RbI and CuI additions also contribute to an improved polycrystalline CsI alloy with outstanding multispectral infrared transmittance properties. 6 figs.

  4. Cooperative dual palladium/silver catalyst for direct difluoromethylation of aryl bromides and iodides.

    PubMed

    Gu, Yang; Leng, Xuebing; Shen, Qilong

    2014-01-01

    Difluoromethylated arenes are one of the privileged structural motifs that are important for fine tuning the biological properties of drug molecules. No general catalytic method exists for the formation of difluoromethylarenes. Previous methods for the preparation of difluoromethylarenes typically required harsh conditions, multiple steps or stoichiometric amount of catalysts. Here we report a cooperative dual palladium/silver catalyst system for direct difluoromethylation of aryl bromides and iodides under mild conditions. We develop the system by initial preparation of the putative intermediates in the dual-catalytic cycles, followed by studying the elemental steps to demonstrate the viability of the proposed cooperative catalytic cycle. The reaction is compatible with a variety of functional groups such as ester, amide, protected phenoxide, protected ketone, cyclopropyl, bromide and heteroaryl subunits such as pyrrole, benzothiazole, carbazole or pyridine. PMID:25377759

  5. Electrical and dielectric properties of silver iodide doped selenium molybdate glassy conductors

    NASA Astrophysics Data System (ADS)

    Palui, A.; Deb, B.; Ghosh, A.

    2013-08-01

    Electrical conductivity and dielectric properties of silver iodide doped silver ion mixed-former conducting glasses have been studied in this paper. The frequency dependence of conductivity has been analyzed following the random free-energy barrier model. The charge carrier relaxation time and the activation energy for relaxation have been determined for the present glasses. The applicability of Barton-Nakajima-Namikawa relation has been tested for the present glasses using the results obtained from random free-energy barrier model. The scaling of the conductivity spectra has been performed to understand the effect of temperature as well as composition on the relaxation dynamics. The dielectric data have been analyzed employing the Cole-Cole function, and parameters such as dielectric strength and Cole-Cole exponent have been obtained. The electrode polarization phenomenon for the present glass samples has been studied depending on temperature as well as composition. The different characteristic transitions concerning electrode polarization related to the charge transport at the interface have been obtained and are correlated to the bulk behavior. An estimation of the dc conductivity has been obtained using the result obtained from electrode polarization study and is observed to be very close to the experimental values.

  6. Diffusional analysis of the adsorption of methyl iodide on silver exchanged mordenite

    SciTech Connect

    Jubin, R.T.; Counce, R.M.

    1997-08-01

    The removal of organic iodides from off-gas streams is an important step in controlling the release of radioactive iodine to the environment during the treatment of radioactive wastes or the processing of some irradiated materials. Nine-well accepted mass transfer models were evaluated for their ability to adequately explain the observed CH{sub 3}I uptake behavior onto the Ag{degrees}Z. Linear and multidimensional regression techniques were used to estimate the diffusion constants and other model parameters, which then permitted the selection of an appropriate mass transfer model. Although a number of studies have been conducted to evaluate the loading of both elemental and methyl iodide on silver-exchanged mordenite, these studies focused primarily on the macro scale (deep bed) while evaluating the material under a broad range of process conditions and contaminants for total bed loading at the time of breakthrough. A few studies evaluated equilibrium or maximum loading. Thus, to date, only bulk loading data exist for the adsorption of CH{sub 3}I onto Ag{degrees}Z. Hence this is believed to be the first study to quantify the controlling mass transfer mechanisms of this process, It can be concluded from the analysis of the experimental data obtained by the {open_quotes}single-pellet{close_quotes} type experiments and for the process conditions used in this study that the overall mass transfer rate associated with the adsorption of CH{sub 3}I onto Ag{degrees}Z is affected by both micropore and macropore diffusion. The macropore diffusion rate was significantly faster than the micropore diffusion, resulting in a two-step adsorption behavior which was adequately modeled by a bimodal pore distribution model. The micropore diffusivity was determined to be on the order of 2 x 10{sup -14} cm{sup 2}/s. The system was also shown to be isothermal under all conditions of this study. 21 refs., 6 figs., 8 tabs.

  7. Conjugated polyelectrolyte-stabilized silver nanoparticles coupled with pyrene derivative for ultrasensitive fluorescent detection of iodide.

    PubMed

    Xiao, Yi; Zhang, Ye; Huang, Hongmei; Zhang, Youyu; Du, Beilei; Chen, Fang; Zheng, Qiao; He, Xiaoxiao; Wang, Kemin

    2015-01-01

    A new sensing system is developed for selective and ultrasensitive detection of iodide based on the inner filter effect (IFE) between conjugated polyelectrolyte-stabilized silver nanoparticles (P1-AgNPs) and 4-oxo-4-(pyren-1-ylmethoxy) butanoic acid (probe 1). P1-AgNPs are designed to be capable of functioning as a composite light-absorber. Meanwhile, probe 1 is selected as an ideal fluorophore because its emission spectrum can perfectly overlap with the absorption band of P1-AgNPs. The intense fluorescence of probe 1 quenched by P1-AgNPs can be efficiently recovered after adding H2O2 and I(-) via the oxidation-etching and regeneration of P1-AgNPs. Under the optimum conditions, this facile IFE-based approach allows the sensitive and selective determination of I(-) in tap water, iodized salt and urine with the detection limit as low as 0.3 nM (S/N=3). Interestingly, the regenerated AgNPs is in smaller size and well-dispersed perhaps due to the particular role of P1 as a polymer localizer containing pyridinyl and sulfonate groups. PMID:25281159

  8. Behavior of the low-frequency conductivity of silver iodide nanocomposites in the superionic phase transition region

    NASA Astrophysics Data System (ADS)

    Vergent'ev, T. Yu.; Koroleva, E. Yu.; Kurdyukov, D. A.; Naberezhnov, A. A.; Filimonov, A. V.

    2013-01-01

    The behavior of the specific conductivity of composites based on silver iodide embedded in porous glasses with an average pore diameter of 7 ± 1 nm and in artificial opals with a pore diameter of 40-100 nm has been investigated in the temperature range from 300 to 500 K. It has been shown that a decrease in the characteristic pore size does not lead to a change in the order of the phase transition and that the temperature of the transition to the superionic state of silver iodide in a porous glass and in an opal upon heating is close to the phase transition temperature T c in the bulk material (˜420 K). Upon cooling, the phase transition temperature T c significantly decreases, and the phase transition becomes diffuse. With a decrease in the pore size, the region of the temperature hysteresis of the phase transition increases. The dc conductivities of the composites have been estimated from the impedance diagrams. The temperature dependence of the dc conductivity of both composites has a thermally activated nature, and the slope of the curve σ(1/ T) changes near the phase transition, which indicates a change in the activation energy. The activation energies in the low-temperature and high-temperature phases have been estimated at ˜450-470 and ˜100 meV, respectively. The equivalent electrical circuit describing the charge transfer processes in the studied samples has been proposed.

  9. On the Radiolytic Decomposition of Colloidal Silver Iodide in Aqueous Suspension

    SciTech Connect

    Guentay, Salih; Cripps, Robin C.; Jaeckel, Bernd; Bruchertseifer, Horst

    2005-06-15

    The decomposition of aqueous colloidal suspensions of AgI induced by ionizing radiation was investigated under various conditions using {sup 188}Re as an in situ beta-radiation source. The suspensions were stabilized by an initial excess of either I{sup -} or Ag{sup +} ions. Although the results were somewhat scattered, the following trends were observed. With an initial excess of I{sup -} and under strong oxidizing conditions (N{sub 2}O sparging) at pH 2, {approx}65% AgI was decomposed into nonvolatile and volatile iodine (ratio 2:1) for doses of {approx}20 kGy, and up to {approx}80% was decomposed (mostly nonvolatile iodine) at pH 5. Chloride ions greatly enhanced the volatile and lowered the nonvolatile fractions. Little decomposition (<10%) was obtained with air sparging at both pH 2 and pH 5. Chloride ions increased the maximum decompositions to {approx}60% ({approx}47% volatile) and {approx}20% (mainly nonvolatile iodine), respectively. With an initial excess of Ag{sup +} with N{sub 2}O sparging and at pH 2 and pH 5, very little volatile iodine was produced. The maximum decomposition was {approx}20% after {approx}20 kGy. Chloride ion addition at pH 2 had greatly enhanced the volatile iodine yield. The relevance of these results to the possible release of iodine to the environment following a nuclear reactor accident is discussed.

  10. Virgin silver nanoparticles as colorimetric nanoprobe for simultaneous detection of iodide and bromide ion in aqueous medium

    NASA Astrophysics Data System (ADS)

    Bothra, Shilpa; Kumar, Rajender; Pati, Ranjan K.; Kuwar, Anil; Choi, Heung-Jin; Sahoo, Suban K.

    2015-10-01

    A simple colorimetric nanoprobe based on virgin silver nanoparticles (AgNPs) was developed for the selective detection of iodide and bromide ions via aggregation and anti-aggregation mechanism. With addition of I- ions, virgin AgNPs, in presence of Fe3+, showed perceptible color change from yellow to colorless along with disappearance of surface plasmon resonance (SPR) band of AgNPs at 400 nm. But in presence of Cr3+, AgNPs turned yellow upon addition of I-and Br- anions. The developed virgin AgNPs probe showed high specificity and selectivity with the detection limits down to 0.32 μM and 1.32 μM for I- ions via two different mechanistic routes. Also, the designed probe detects Br- with a detection limit down to 1.67 μM.

  11. Virgin silver nanoparticles as colorimetric nanoprobe for simultaneous detection of iodide and bromide ion in aqueous medium.

    PubMed

    Bothra, Shilpa; Kumar, Rajender; Pati, Ranjan K; Kuwar, Anil; Choi, Heung-Jin; Sahoo, Suban K

    2015-01-01

    A simple colorimetric nanoprobe based on virgin silver nanoparticles (AgNPs) was developed for the selective detection of iodide and bromide ions via aggregation and anti-aggregation mechanism. With addition of I(-) ions, virgin AgNPs, in presence of Fe(3+), showed perceptible color change from yellow to colorless along with disappearance of surface plasmon resonance (SPR) band of AgNPs at 400 nm. But in presence of Cr(3+), AgNPs turned yellow upon addition of I(-)and Br(-) anions. The developed virgin AgNPs probe showed high specificity and selectivity with the detection limits down to 0.32 μM and 1.32 μM for I(-) ions via two different mechanistic routes. Also, the designed probe detects Br(-) with a detection limit down to 1.67 μM. PMID:25950637

  12. Removal of bromide and iodide anions from drinking water by silver-activated carbon aerogels.

    PubMed

    Sánchez-Polo, M; Rivera-Utrilla, J; Salhi, E; von Gunten, U

    2006-08-01

    The aim of this study is to analyze the use of Ag-doped activated carbon aerogels for bromide and iodide removal from drinking water and to study how the activation of Ag-doped aerogels affects their behavior. It has been observed that the carbonization treatment and activation process of Ag-doped aerogels increased the surface area value ( [Formula: see text] ), whereas the volume of meso-(V(2)) and macropores (V(3)) decreased slightly. Chemical characterization of the materials revealed that carbonization and especially activation process considerably increased the surface basicity of the sample. Original sample (A) presented acidic surface properties (pH(PZC)=4.5) with 21% surface oxygen, whereas the sample that underwent activation showed mainly basic surface chemical properties (pH(PZC)=9.5) with only 6% of surface oxygen. Carbonization and especially, activation process considerable increased the adsorption capacity of bromide and iodide ions. This would mainly be produced by (i) an increase in the microporosity of the sample, which increases Ag-adsorption sites available to halide anions, and (ii) a rise of the basicity of the sample, which produces an increase in attractive electrostatic interactions between the aerogel surface, positively charged at the working pH (pH(solution)iodide was studied under dynamic conditions using waters from Lake Zurich. Results obtained showed that the carbonization and activation processes increased the adsorptive capacity of the aerogel sample. However, results showed that the adsorption capacity of the aerogel samples studied was considerably lower in water from Lake Zurich. Results showed X(0.02) (amount adsorbed to initial breakthrough) values of 0.1 and 4.3 mg/g for chloride anion and dissolved organic carbon (DOC), respectively, during bromide adsorption process in water from Lake Zurich

  13. Experimental studies of silver iodide pyrotechnic aerosol ice forming efficiency dynamics

    NASA Astrophysics Data System (ADS)

    Shilin, A. G.; Drofa, A. S.; Ivanov, V. N.; Savchenko, A. V.; Shilin, V. A.

    2013-05-01

    The study concerns the problems connected with the temporal variability of aerosol ice forming activity at introduction into the sub-cloud layer and the comparison of aerosol efficiency of produced pyrotechnic mixtures with different silver contents.

  14. Cesium iodide alloys

    SciTech Connect

    Kim, Hyoun-Ee; Moorhead, A.J.

    1991-01-01

    This invention relates to a CsI composition with improved mechanical strength and outstanding multispectral infrared transmittance, for window use. The additive is a monovalent iodide, other than CsI, added in amounts sufficient to maximize fracture strength from 16 to 40 MPa, while maintaining at least 10% transparency in the 4 to 50 micrometer wavelength range. The preferred additive is AgI, although RbI or CuI can be used. 6 figs. (DLC)

  15. Silver diffusion and isotope effect in silver rubidium iodide. [RbAg/sub 4/I/sub 5/

    SciTech Connect

    Arzigian, James Simon

    1980-01-01

    The diffusion coefficient of silver in RbAg/sub 4/I/sub 5/ was measured in both superionic phases using radiotracer Ag-110m and serial sectioning with a low temperature sectioning apparatus. The activation energies for diffusion in alpha-RbAg/sub 4/I/sub 5/ and beta-RbAg/sub 4/I/sub 5/, respectively, are 0.11 +- 0.01 eV and 0.20 +- 0.04 eV. An isotope effect for diffusion was also measured in both superionic phases. Ag-105 and Ag-110m radioisotopes were used with gamma spectroscopy and energy discrimination. The effect is small, with no significant temperature variation, with the value at 333/sup 0/K being 0.12 +- 0.01. The second-order phase transition at 208/sup 0/K has a small effect, if any, on the magnitude of the effect. The data suggest that a highly cooperative transport mechanism is responsible for the unusually high values of both the conductivity and diffusion coefficient. Although it is not possible to deduce the particular mechanism involved, theories inolving ionic polarons, or cooperative motion, such as crowdions or solitons, seem consistent with the observed results.

  16. AgI-coated silver-clad stainless steel hollow waveguides for infrared lightwave transmission and their applications.

    PubMed

    Hongo, Akihito; Sato, Shinobu; Hattori, Akio; Iwai, Katsumasa; Takaku, Hiroyuki; Miyagi, Mitsunobu

    2012-01-01

    We fabricated silver iodide (AgI)-coated silver hollow waveguides to transmit a wide range of infrared (IR) light. Silver-clad stainless steel pipes were used as a supporting pipe. Since this type of metallic hollow waveguide has high mechanical strength and heat resistance, it is suitable as a rigid lightwave probe for various applications such as dental or medical laser treatment, IR spectroscopy, thermal radiometry, and laser processing. Considering these applications, we estimated the hollow waveguides with different thicknesses of the AgI layer. By optimizing the AgI layer thickness according to the wavelength of propagating light, we succeeded in efficiently transmitting Er-YAG and CO(2) laser light. We also studied the optical characteristics of a wide range of incoherent light for IR spectroscopy and radiometry applications using these metallic hollow waveguides as lightwave probes. PMID:22270406

  17. Structural Evidence for a Fast-Ion Transition in the High-Pressure Rocksalt Phase of Silver Iodide

    NASA Astrophysics Data System (ADS)

    Keen, D. A.; Hull, S.; Hayes, W.; Gardner, N. J. G.

    1996-12-01

    This Letter describes neutron diffraction measurements of the rocksalt structured phase of AgI at high pressure and temperature and the structural disorder which accompanies its high conductivity. In contrast to the first-order structural phase transition which results in fast-ionic α-AgI at ambient pressure, the fast-ionic behavior in rocksalt structured AgI occurs above a diffuse transition with a small anomaly in lattice parameter and a continuous increase in occupation of interstitial tetrahedral sites with increasing temperature. There are approximately 10 times more defects in the fast-ionic phase of rocksalt AgI than in isostructural AgBr at ambient pressure, 1 K below melting.

  18. Scintillation properties of the silver doped lithium iodide single crystals at room and low temperature

    NASA Astrophysics Data System (ADS)

    Khan, Sajid; Kim, H. J.; Lee, M. H.

    2016-06-01

    This study presents luminescence and scintillation properties of Silver doped LiI crystals. Single crystals of LiI: x% Ag (x=0.02, 0.05, 0.1 and 0.5) were grown by using the Bridgman technique. X-ray induced luminescence spectra show emission bands spanning from 275 nm to 675 nm, dominated by Ag+ band having a peak at 300 nm. Under UV-luminescence, a similar emission band was observed with the peak excitation wavelength of 265 nm. Energy resolution, light yield and decay time profiles of the samples were measured under a 137Cs γ-ray irradiation. The LiI(0.1%Ag) showed the highest light yield and the best energy resolution among the samples. The light yield of LiI(0.1%Ag) is higher than commercially available LiI(Eu) crystal (15,000±1500 ph/MeV). The LiI(Ag) samples exhibit three exponential decay time components except the LiI(0.02%Ag), where the fitting found two decay time components. Temperature dependences of emission spectra, light yield and decay time were studied from 300 K to 10 K. The LiI(0.1%Ag) crystal showed an increase in the light yield and a shortening of decay time with a decrease in temperature..

  19. Reactions of VX, HD, and their simulants with NaY and AgY zeolites. Desulfurization of VX on AgY

    SciTech Connect

    Wagner, G.W.; Bartram, P.W.

    1999-11-09

    The room-temperature reactions of the chemical warfare agents VX (O-ethyl S-2-(diisopropylamino)-ethyl methylphosphonothioate), HD (2,2{prime}-dichloroethyl sulfide, or mustard), and their common simulants, O,S-diethyl phenylphosphonothioate (DEPPT) and 2-chloroethyl phenyl sulfide (CEPS), with NaY and silver-exchanged (AgY) zeolites have been studied using solid-state magic angle spinning NMR. VX hydrolyzes via exclusive cleavage of the P{single{underscore}bond}S bond on both NaY and AgY to yield ethyl methylphosphonate (EMPA). The reaction is significantly faster on AgY than on NaY, suggesting catalysis by silver. On AgY, an intermediate silver salt of EMPA is apparently formed which is slowly converted to ethyl 2-(diisopropylamino)ethyl methylphosphonate (QB, the desulfurized analogue of VX) in about a 78% yield. DEPPT similarly hydrolyzes via P{single{underscore}bond}S cleavage on AgY to yield an apparent silver salt of ethyl phenylphosphonate, which does not undergo further reaction to the desulfurized analogue. No reaction is observed for DEPPT on NaY. HD on AgY forms both vinyl sulfide and the cyclic ether 1,4-thioxane. HD reacts faster on NaY to exclusively form the CH-TG sulfonium ion (HOCH{sub 2}CH{sub 2}SCH{sub 2}CH{sub 2}S{sup +}[CH{sub 2}CH{sub 2}OH]{sub 2}). CEPS also reacts faster on NaY, forming 2-hydroxyethyl phenyl sulfide. On AgY, CEPS does not give the vinyl product, but does yield the ether product PhSCH{sub 2}CH{sub 2}OCH{sub 2}CH{sub 2}SPh. A mechanism is proposed for the silver-catalyzed hydrolysis of VX, the desulfurization of the cleaved thiol, and the formation of QB.

  20. Responses to catastrophic AGI risk: a survey

    NASA Astrophysics Data System (ADS)

    Sotala, Kaj; Yampolskiy, Roman V.

    2015-01-01

    Many researchers have argued that humanity will create artificial general intelligence (AGI) within the next twenty to one hundred years. It has been suggested that AGI may inflict serious damage to human well-being on a global scale (‘catastrophic risk’). After summarizing the arguments for why AGI may pose such a risk, we review the field's proposed responses to AGI risk. We consider societal proposals, proposals for external constraints on AGI behaviors and proposals for creating AGIs that are safe due to their internal design.

  1. Charge carrier mobility and concentration as a function of composition in AgPO3-AgI glasses

    NASA Astrophysics Data System (ADS)

    Rodrigues, Ana Candida Martins; Nascimento, Marcio Luis Ferreira; Bragatto, Caio Barca; Souquet, Jean-Louis

    2011-12-01

    Conductivity data of the xAgI(1 - x)AgPO3 system (0 ≤ x ≤ 0.5) were collected in the liquid and glassy states. The difference in the dependence of ionic conductivity on temperature below and above their glass transition temperatures (Tg) is interpreted by a discontinuity in the charge carrier's mobility mechanisms. Charge carrier displacement occurs through an activated mechanism below Tg and through a Vogel-Fulcher-Tammann-Hesse mechanism above this temperature. Fitting conductivity data with the proposed model allows one to determine separately the enthalpies of charge carrier formation and migration. For the five investigated compositions, the enthalpy of charge carrier formation is found to decrease, with x, from 0.86 to 0.2 eV, while the migration enthalpy remains constant at ≈0.14 eV. Based on these values, the charge carrier mobility and concentration in the glassy state can then be calculated. Mobility values at room temperature (≈10-4 cm2 V-1 s-1) do not vary significantly with the AgI content and are in good agreement with those previously measured by the Hall-effect technique. The observed increase in ionic conductivity with x would thus only be due to an increase in the effective charge carrier concentration. Considering AgI as a weak electrolyte, the change in the effective charge carrier concentration is justified and is correlated to the partial free energy of silver iodide forming a regular solution with AgPO3.

  2. Generation and loss of radicals from the decomposition of methyl iodide, diallyl, and butyl halides on a silver catalyst

    SciTech Connect

    Garibyan, T.A.; Grigoryan, R.R.; Muradyan, A.A.; Nalbandyan, A.B.

    1987-12-01

    The stages of the generation and loss of CH/sub 3/O/sub 2/, C/sub 3/H/sub 5/O/sub 2/, and C/sub 4/H/sub 9/O/sub 2/ radicals in the decomposition of CH/sub 3/I, (C/sub 3/H/sub 5/)/sub 2/, C/sub 4/H/sub 9/Br, C/sub 4/H/sub 9/Cl, and C/sub 4/H/sub 9/I, respectively, have been studied in the presence of oxygen on Ag/pumice. Effective energies of activation for generation of these radicals have been calculated. It has been found that heterogeneously catalyzed decomposition of these compounds begins on the silver surface at low temperatures (400-590 K) and is accompanied by desorption of the radicals from the surface of the catalyst to the gas phase. It has also been demonstrated that in the indicated temperature range on the silver catalyst allyl peroxy radicals are stable, bu that the CH/sub 3/O/sub 2/ and C/sub 4/H/sub 9/O/sub 2/ radicals disappear to a small extent (10 and 23%, respectively).

  3. A novel silver iodide metalo-drug: experimental and computational modelling assessment of its interaction with intracellular DNA, lipoxygenase and glutathione.

    PubMed

    Banti, C N; Kyros, L; Geromichalos, G D; Kourkoumelis, N; Kubicki, M; Hadjikakou, S K

    2014-04-22

    The new mixed ligand silver(I) complex of formula [AgI(TPP)2(MBZT)] (1) was obtained by reacting 2-mercapto-benzothiazole (MBZT) with triphenylphosphine (TPP). The complex was characterized by m.p., vibrational spectroscopy (FT-IR), (1)H NMR, UV-vis, ESI-MS spectroscopic techniques and its structure was confirmed by X-ray crystallography. Mixed ligand complexes of silver(I) iodide with thiones and phosphines are very rare in the literature and to the best of our knowledge compound 1 is the first of this kind exhibiting significant biological effects. Complex 1 was evaluated for its in vitro cytotoxic activity (cell viability) under irradiation with UV light and without irradiation against human cancer cell lines: MCF-7 (breast, ER positive), MDA-MB-231 (breast, ER negative), Caki-1 (renal), A549 (lung), OAW-42 (ovarian), HeLa (cervical) and additionally against the normal human lung cell line MRC-5 (normal human fetal lung fibroblast cells) and normal immortalized human mammary gland epithelial cell line (MTSV17) with SRB assay. The results showed that 1 mediates a strong cytotoxic response to the tested normal and cancer cell lines. It exhibits equal activity against MDA-MB-231 cells where estrogen receptors (ERs) are devoid with the one against MCF-7 where ERs are present. Molecular docking studies have shown that 1 is docked in the different pocket than that of the ERs modulators. The binding affinity of 1 towards the intracellular molecules DNA and lipoxygenase (LOX) was studied for the evaluation of the mechanism of its cytostasis. The binding constant (Kb) of 1 towards CT-DNA was calculated by UV-Vis and fluorescent spectra suggesting intercalation or electrostatic interactions of 1 into DNA. Docking studies on DNA-complex interactions confirm the binding of 1. Moreover, the influence of complex 1 on the catalytic peroxidation of linoleic acid to hydroperoxylinoleic acid by the enzyme lipoxygenase (LOX) was kinetically and theoretically studied. In addition

  4. Electrodeposition as an alternate method for preparation of environmental samples for iodide by AMS

    SciTech Connect

    Adamic, M. L.; Lister, T. E.; Dufek, E. J.; Jenson, D. D.; Olson, J. E.; Vockenhuber, C.; Watrous, M. G.

    2015-03-25

    This paper presents an evaluation of an alternate method for preparing environmental samples for 129I analysis by accelerator mass spectrometry (AMS) at Idaho National Laboratory. The optimal sample preparation method is characterized by ease of preparation, capability of processing very small quantities of iodide, and ease of loading into a cathode. Electrodeposition of iodide on a silver wire was evaluated using these criteria. This study indicates that the electrochemically-formed silver iodide deposits produce ion currents similar to those from precipitated silver iodide for the same sample mass. Furthermore, precipitated silver iodide samples are usually mixed with niobium or silver powder prior to loading in a cathode. Using electrodeposition, the silver is already mixed with the sample and can simply be picked up with tweezers, placed in the sample die, and pressed into a cathode. The major advantage of this method is that the silver wire/electrodeposited silver iodide is much easier to load into a cathode.

  5. Electrodeposition as an alternate method for preparation of environmental samples for iodide by AMS

    NASA Astrophysics Data System (ADS)

    Adamic, M. L.; Lister, T. E.; Dufek, E. J.; Jenson, D. D.; Olson, J. E.; Vockenhuber, C.; Watrous, M. G.

    2015-10-01

    This paper presents an evaluation of an alternate method for preparing environmental samples for 129I analysis by accelerator mass spectrometry (AMS) at Idaho National Laboratory. The optimal sample preparation method is characterized by ease of preparation, capability of processing very small quantities of iodide, and ease of loading into a cathode. Electrodeposition of iodide on a silver wire was evaluated using these criteria. This study indicates that the electrochemically-formed silver iodide deposits produce ion currents similar to those from precipitated silver iodide for the same sample mass. Precipitated silver iodide samples are usually mixed with niobium or silver powder prior to loading in a cathode. Using electrodeposition, the silver is already mixed with the sample and can simply be picked up with tweezers, placed in the sample die, and pressed into a cathode. The major advantage of this method is that the silver wire/electrodeposited silver iodide is much easier to load into a cathode.

  6. A colorimetric assay for measuring iodide using Au@Ag core-shell nanoparticles coupled with Cu(2+).

    PubMed

    Zeng, Jingbin; Cao, Yingying; Lu, Chun-Hua; Wang, Xu-Dong; Wang, Qianru; Wen, Cong-Ying; Qu, Jian-Bo; Yuan, Cunguang; Yan, Zi-Feng; Chen, Xi

    2015-09-01

    Au@Ag core-shell nanoparticles (NPs) were synthesized and coupled with copper ion (Cu(2+)) for the colorimetric sensing of iodide ion (I(-)). This assay relies on the fact that the absorption spectra and the color of metallic core-shell NPs are sensitive to their chemical ingredient and dimensional core-to-shell ratio. When I(-) was added to the Au@Ag core-shell NPs-Cu(2+) system/solution, Cu(2+) can oxidize I(-) into iodine (I2), which can further oxidize silver shells to form silver iodide (AgI). The generated Au@AgI core-shell NPs led to color changes from yellow to purple, which was utilized for the colorimetric sensing of I(-). The assay only took 10 min with a lowest detectable concentration of 0.5 μM, and it exhibited excellent selectivity for I(-) over other common anions tested. Furthermore, Au@Ag core-shell NPs-Cu(2+) was embedded into agarose gels as inexpensive and portable "test strips", which were successfully used for the semi-quantitation of I(-) in dried kelps. PMID:26388386

  7. Potassium Iodide

    MedlinePlus

    ... radioactive iodine that may be released during a nuclear radiation emergency. Radioactive iodine can damage the thyroid gland. ... only take potassium iodide if there is a nuclear radiation emergency and public officials tell you that you ...

  8. Potassium Iodide

    MedlinePlus

    Potassium iodide is used to protect the thyroid gland from taking in radioactive iodine that may be released during a nuclear radiation emergency. Radioactive iodine can damage the thyroid gland. You ...

  9. MICROWAVE SPECTRA AND GEOMETRIES OF C2H_{2\\cdots AgI} and C2H_{4\\cdots AgI}

    NASA Astrophysics Data System (ADS)

    Stephens, Susanna L.; Tew, David Peter; Walker, Nick; Legon, Anthony

    2015-06-01

    A chirped-pulse Fourier transform microwave spectrometer has been used to measure the microwave spectra of both C2H_{2\\cdots AgI} and C2H_{4\\cdots AgI}. These complexes are generated via laser ablation at 532 nm of a silver surface in the presence of CF3I and either C2H_{2} or C2H_{4} and argon and are stabilized by a supersonic expansion. Rotational (A0, B0, C0) and centrifugal distortion constants (ΔJ and ΔJK) of each molecule have been determined as well the nuclear electric quadrupole coupling constants the iodine atom (χaa(I) and χbb-χcc(I)). The spectrum of each molecule is consistent with a C2v structure in which the metal atom interacts with the π-orbital of the ethene or ethyne molecule. Isotopic substitutions of atoms within the C2H_{2} or C2H_{4} subunits are in progress and in conjunction with high level ab initio calculations will allow for accurate determination of the geometry of each molecule. These to complexes are put in the context of the recently studied H2S\\cdots AgI, OC\\cdotsAgI, H3N\\cdots AgI and (CH3)_{3N\\cdots AgI}. S.Z. Riaz, S.L. Stephens, W. Mizukami, D.P. Tew, N.R. Walker, A.C. Legon, Chem. Phys. Let., 531, 1-12 (2012) S.L. Stephens, W. Mizukami, D.P. Tew, N.R. Walker, A.C. Legon, J. Chem. Phys., 136(6), 064306 (2012) D.M. Bittner, D.P. Zaleski, S.L. Stephens, N.R. Walker, A.C. Legon, Study in progress.

  10. A new silver ion conducting SbI3-Ag4P2O7 nanocomposite solid electrolyte

    NASA Astrophysics Data System (ADS)

    Suthanthiraraj, S. Austin; Sarumathi, R.

    2013-12-01

    This paper presents an investigation on a new series of silver ion conducting nanocomposite materials of silver pyrophosphate-based solid electrolytes with various amounts of antimony iodide. The detailed electrical conductivity studies carried out by impedance spectroscopic analysis in the frequency range from 20 Hz to 1 MHz have shown that silver ionic conductivity attains a maximum value of 4.1 × 10-4 S cm-1 at room temperature for the typical composition having 60 mol% of SbI3. Powder samples characterized by X-ray diffraction, Fourier transform infrared spectroscopy, differential scanning calorimetric analysis and silver ionic transport studies were identified to indicate the existence of AgI, in addition to certain new phases in all the different compositions of the system. The conduction channel for Ag+ ions across phosphate network was found to get expanded by the presence of iodide ion. The formation of P-O-M (M=Sb3+) within the crystal structure is also favoured, where Sb3+ ions may serve as ionic cross-links between non-bridging oxygen of different phosphate groups. The field emission scanning electron microscopic investigations of their microstructures have suggested the presence of nanocomposites, leading to the observed electrical conductivity data coupled with many interesting features closely related to the particle size and practical application as solid electrolyte for the fabrication of solid-state battery at ambient conditions.

  11. Silver

    Integrated Risk Information System (IRIS)

    Silver ; CASRN 7440 - 22 - 4 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic Effects )

  12. Methyl iodide

    Integrated Risk Information System (IRIS)

    Methyl iodide ; CASRN 74 - 88 - 4 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic Effe

  13. Methyl Iodide

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Methyl iodide (MeI, iodomethane, CH3I) was reported as a potential alternative to the stratospheric ozone-depleting fumigant methyl bromide (MeBr) in the mid-1990s (Sims et al., 1995; Ohr et al., 1996). It has since received significant research attention to determine its environmental fate and tran...

  14. Silver-mordenite for radiologic gas capture from complex streams. Dual catalytic CH3I decomposition and I confinement

    DOE PAGESBeta

    Nenoff, Tina M.; Rodriguez, Mark A.; Soelberg, Nick R.; Chapman, Karena W.

    2014-05-09

    The selective capture of radiological iodine (129I) is a persistent concern for safe nuclear energy. In these nuclear fuel reprocessing scenarios, the gas streams to be treated are extremely complex, containing several distinct iodine-containing molecules amongst a large variety of other species. Silver-containing mordenite (MOR) is a longstanding benchmark for radioiodine capture, reacting with molecular iodine (I2) to form AgI. However the mechanisms for organoiodine capture is not well understood. Here we investigate the capture of methyl iodide from complex mixed gas streams by combining chemical analysis of the effluent gas stream with in depth characterization of the recovered sorbent.more » Tools applied include infrared spectroscopy, thermogravimetric analysis with mass spectrometry, micro X-ray fluorescence, powder X-ray diffraction analysis, and pair distribution function analysis. Moreover, the MOR zeolite catalyzes decomposition of the methyl iodide through formation of surface methoxy species (SMS), which subsequently reacts with water in the mixed gas stream to form methanol, and with methanol to form dimethyl ether, which are both detected downstream in the effluent. The liberated iodine reacts with Ag in the MOR pore to the form subnanometer AgI clusters, smaller than the MOR pores, suggesting that the iodine is both physically and chemically confined within the zeolite.« less

  15. Surface and zeta-potentials of silver halide single crystals: pH-dependence in comparison to particle systems.

    PubMed

    Selmani, Atiða; Lützenkirchen, Johannes; Kallay, Nikola; Preočanin, Tajana

    2014-06-18

    We have carried out surface and zeta-potential measurements on AgCl and AgBr single crystals. As for particle systems we find that, surprisingly and previously unnoted, the zeta-potential exhibits pH-dependence, while the surface potential does not. A possible interpretation of these observations is the involvement of water ions in the interfacial equilibria and in particular, stronger affinity of the hydroxide ion compared to the proton. The pH-dependence of the zeta-potential can be suppressed at sufficiently high silver concentrations, which agrees with previous measurements in particle systems where no pH-dependence was found at high halide ion concentrations. The results suggest a subtle interplay between the surface potential determining the halide and silver ion concentrations, and the water ions. Whenever the charge due to the halide and silver ions is sufficiently high, the influence of the proton/hydroxide ion on the zeta-potential vanishes. This might be related to the water structuring at the relevant interfaces which should be strongly affected by the surface potential. Another interesting observation is accentuation of the assumed water ion effect on the zeta-potential at the flat single crystal surfaces compared to the corresponding silver halide colloids. Previous generic MD simulations have indeed predicted that hydroxide ion adsorption is accentuated on flat/rigid surfaces. A thermodynamic model for AgI single crystals was developed to describe the combined effects of iodide, silver and water ions, based on two independently previously published models for AgI (that only consider constituent and background electrolyte ions) and inert surfaces (that only consider water and background electrolyte ions). The combined model correctly predicts all the experimentally observed trends. PMID:24863080

  16. Cesium iodide crystals fused to vacuum tube faceplates

    NASA Technical Reports Server (NTRS)

    Fleck, H. G.

    1964-01-01

    A cesium iodide crystal is fused to the lithium fluoride faceplate of a photon scintillator image tube. The conventional silver chloride solder is then used to attach the faceplate to the metal support.

  17. Silver-mordenite for radiologic gas capture from complex streams. Dual catalytic CH3I decomposition and I confinement

    SciTech Connect

    Nenoff, Tina M.; Rodriguez, Mark A.; Soelberg, Nick R.; Chapman, Karena W.

    2014-05-09

    The selective capture of radiological iodine (129I) is a persistent concern for safe nuclear energy. In these nuclear fuel reprocessing scenarios, the gas streams to be treated are extremely complex, containing several distinct iodine-containing molecules amongst a large variety of other species. Silver-containing mordenite (MOR) is a longstanding benchmark for radioiodine capture, reacting with molecular iodine (I2) to form AgI. However the mechanisms for organoiodine capture is not well understood. Here we investigate the capture of methyl iodide from complex mixed gas streams by combining chemical analysis of the effluent gas stream with in depth characterization of the recovered sorbent. Tools applied include infrared spectroscopy, thermogravimetric analysis with mass spectrometry, micro X-ray fluorescence, powder X-ray diffraction analysis, and pair distribution function analysis. Moreover, the MOR zeolite catalyzes decomposition of the methyl iodide through formation of surface methoxy species (SMS), which subsequently reacts with water in the mixed gas stream to form methanol, and with methanol to form dimethyl ether, which are both detected downstream in the effluent. The liberated iodine reacts with Ag in the MOR pore to the form subnanometer AgI clusters, smaller than the MOR pores, suggesting that the iodine is both physically and chemically confined within the zeolite.

  18. Adsorption Behavior of Cellulose and Its Derivatives toward Ag(I) in Aqueous Medium: An AFM, Spectroscopic, and DFT Study.

    PubMed

    Zhu, Chuantao; Dobryden, Illia; Rydén, Jens; Öberg, Sven; Holmgren, Allan; Mathew, Aji P

    2015-11-17

    The aim of this study was to develop a fundamental understanding of the adsorption behavior of metal ions on cellulose surfaces using experimental techniques supported by computational modeling, taking Ag(I) as an example. Force interactions among three types of cellulose microspheres (native cellulose and its derivatives with sulfate and phosphate groups) and the silica surface in AgNO3 solution were studied with atomic force microscopy (AFM) using the colloidal probe technique. The adhesion force between phosphate cellulose microspheres (PCM) and the silica surface in the aqueous AgNO3 medium increased significantly with increasing pH while the adhesion force slightly decreased for sulfate cellulose microspheres (SCM), and no clear adhesion force was observed for native cellulose microspheres (CM). The stronger adhesion enhancement for the PCM system is mainly attributed to the electrostatic attraction between Ag(I) and the negative silica surface. The observed force trends were in good agreement with the measured zeta potentials. The scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR) analyses confirmed the presence of silver on the surface of cellulose microspheres after adsorption. This study showed that PCM with a high content of phosphate groups exhibited a larger amount of adsorbed Ag(I) than CM and SCM and possible clustering of Ag(I) to nanoparticles. The presence of the phosphate group and a wavenumber shift of the P-OH vibration caused by the adsorption of silver ions on the phosphate groups were further confirmed with computational studies using density functional theory (DFT), which gives support to the above findings regarding the adsorption and clustering of Ag(I) on the cellulose surface decorated with phosphate groups as well as IR spectra. PMID:26501836

  19. Physicochemical properties of the anion-modified surfaces of silver nanostructures

    NASA Astrophysics Data System (ADS)

    Sibbald, Morgan Scot

    Nano-sized structures of silver were prepared, characterized, and then chemically-modified with the adsorption of molecules and ions on the metal surface. Nanostructures prepared as aqueous colloids were found to have highly regular polyhedral shapes by transmission electron microscopy. Electron diffraction techniques indicated that isolated Ag structures were composed of a single crystalline phase or were multiply-twinned, both having a lattice constant of 4.05 A. Adsorption of iodide and bromide ions on the silver surface was monitored by surface-enhanced Raman spectroscopy. A characteristic halide-metal stretching vibration was observed at 112 cmsp{-1} for Isp- and at 156 cmsp{-1} for Brsp-. Extinction spectra of the halide-modified Ag colloids showed a frequency-shift and damping of the surface plasmon resonance band assigned to particle aggregation. This was confirmed using two dimensional arrays of particles in which the surface-modifier caused only damping with no change in the plasmon frequency. Addition of cytochrome c to the halide-modified colloid resulted in the reduction of the protein. Competitive binding of Isp- ions between cytochrome c and the metal necessitated the use of a redox active indophenol dye for quantitative measurements of reduction efficiencies. Two distinct processes were identified: reduction at iodide coverages up to one monolayer on the Ag surface and reduction in the presence of excess Isp- in solution. The latter was characterized by Isp- reacting with silver in a 1:1 stoichiometry to form molecular AgI. The former, which resulted in only 5% reduction of the electron acceptors, was a consequence of partial charge transfer from Isp- to the metal, producing a unique iodide-Ag surface complex different than molecular AgI. Raman spectra of the complex excited at 413 nm and at temperatures less than 150 K contained a strong vibrational progression with a fundamental band at 123 cmsp{-1} and up to six overtones. An excitation profile

  20. The Advanced Gamma-ray Imaging System (AGIS) - Simulation Studies

    SciTech Connect

    Maier, G.; Buckley, J.; Bugaev, V.; Fegan, S.; Vassiliev, V. V.; Funk, S.; Konopelko, A.

    2008-12-24

    The Advanced Gamma-ray Imaging System (AGIS) is a US-led concept for a next-generation instrument in ground-based very-high-energy gamma-ray astronomy. The most important design requirement for AGIS is a sensitivity of about 10 times greater than current observatories like Veritas, H.E.S.S or MAGIC. We present results of simulation studies of various possible designs for AGIS. The primary characteristics of the array performance, collecting area, angular resolution, background rejection, and sensitivity are discussed.

  1. The Advanced Gamma-ray Imaging System (AGIS): Simulation studies

    SciTech Connect

    Maier, G.; Buckley, J.; Bugaev, V.; Fegan, S.; Funk, S.; Konopelko, A.; Vassiliev, V.V.; /UCLA

    2011-06-14

    The Advanced Gamma-ray Imaging System (AGIS) is a next-generation ground-based gamma-ray observatory being planned in the U.S. The anticipated sensitivity of AGIS is about one order of magnitude better than the sensitivity of current observatories, allowing it to measure gamma-ray emission from a large number of Galactic and extra-galactic sources. We present here results of simulation studies of various possible designs for AGIS. The primary characteristics of the array performance - collecting area, angular resolution, background rejection, and sensitivity - are discussed.

  2. Synthesis of Ag and AgI quantum dots in AOT-stabilized water-in-CO2 microemulsions.

    PubMed

    Liu, Juncheng; Raveendran, Poovathinthodiyil; Shervani, Zameer; Ikushima, Yutaka; Hakuta, Yukiya

    2005-03-01

    Silver and silver iodide nanocrystals have been synthesized in the water-in-CO(2) reverse microemulsions formed by the commonly used surfactant, sodium bis(2-ethylhexyl)sulfosuccinate (AOT), in the presence of 2,2,3,3,4,4,5,5-octafluoro-1-pentanol as cosurfactant. The nanometer-sized aqueous domains in the microemulsion cores not only act as nanoreactors, but the surfactant interfacial monolayer also helps the stabilization of the metal and semiconductor nanoparticles. The transmission electron microscopy results show that silver and silver iodide nanocrystals with average diameters of 6.0 nm (standard deviation, SD=1.3 nm) and 5.7 nm (SD=1.4 nm), respectively, were formed. The results indicate that the method can be utilized as a general and economically viable approach for the synthesis of metal and semiconductor quantum dots in environmentally benign supercritical carbon dioxide. PMID:15685712

  3. Silver at an old mining camp: Cobalt, Ontario, Canada

    SciTech Connect

    Kramer, J.R.; Adams, N.W.H.; Manolopoulos, H.; Collins, P.V.

    1999-01-01

    Aqueous Ag(I) in different size fractions, <5 {micro}m, <0.2 {micro}m, and <10 kDa, was analyzed in a low dissolved organic carbon (DOC) and a high DOC environment. The sediment and tailings, contacting the water, were elevated in silver from mining. The area is buffered at pH 6 to 8 by carbonate mineral gangue. Aqueous Ag(I) is present at nanogram per liter levels. Significant amounts of Ag are found in the colloidal and are nondetectable or a few nanograms per liter in the <10-kDa fraction. Acid-volatile sulfide (AVS) was found in most (oxic) water samples at the nanomolar level. Ag(I) does not accumulate in plants probably due to the strong binding of Ag(I-) with S(II-). One exception occurs for cattails, when the aqueous AVS concentration is less than the colloidal AG(I) concentration.

  4. Silver Complexes of Dihalogen Molecules.

    PubMed

    Malinowski, Przemysław J; Himmel, Daniel; Krossing, Ingo

    2016-08-01

    The perfluorohexane-soluble and donor-free silver compound Ag(A) (A=Al(OR(F) )4 ; R(F) =C(CF3 )3 ) prepared using a facile novel route has unprecedented capabilities to form unusual and weakly bound complexes. Here, we report on the three dihalogen-silver complexes Ag(Cl2 )A, Ag(Br2 )A, and Ag(I2 )A derived from the soluble silver compound Ag(A) (characterized by single-crystal/powder XRD, Raman spectra, and quantum-mechanical calculations). PMID:27404568

  5. Electrodeposition as an alternate method for preparation of environmental samples for iodide by AMS

    DOE PAGESBeta

    Adamic, M. L.; Lister, T. E.; Dufek, E. J.; Jenson, D. D.; Olson, J. E.; Vockenhuber, C.; Watrous, M. G.

    2015-03-25

    This paper presents an evaluation of an alternate method for preparing environmental samples for 129I analysis by accelerator mass spectrometry (AMS) at Idaho National Laboratory. The optimal sample preparation method is characterized by ease of preparation, capability of processing very small quantities of iodide, and ease of loading into a cathode. Electrodeposition of iodide on a silver wire was evaluated using these criteria. This study indicates that the electrochemically-formed silver iodide deposits produce ion currents similar to those from precipitated silver iodide for the same sample mass. Furthermore, precipitated silver iodide samples are usually mixed with niobium or silver powdermore » prior to loading in a cathode. Using electrodeposition, the silver is already mixed with the sample and can simply be picked up with tweezers, placed in the sample die, and pressed into a cathode. The major advantage of this method is that the silver wire/electrodeposited silver iodide is much easier to load into a cathode.« less

  6. X-ray diffraction on (AgI)0.7- (NaPO3)0.3 and (AgI)0.8- (NaPO3)0.2 composites

    SciTech Connect

    Purwanto, A. . E-mail: purwanto@centrin.net.id; Kartini, E.; Sakuma, T.; Collins, M.F.; Kamiyama, T.

    2005-01-04

    We have identified the crystallographic phases of the melt-quenched superionic composites (AgI)0.7- (NaPO3)0.3 and (AgI)0.8- (NaPO3)0.2 by X-ray diffraction. Measurements were made in a temperature range from 300 to 630 deg. K. The materials have a glass phase and one or more crystalline phases. At 300 deg. K and at 350-bar K, the crystalline phase contains a 30:70 mixture of {beta}AgI and {gamma}AgI. Above 350 deg. K, the fraction of {beta}AgI increases and at 403-bar K it is the dominant phase with a {beta}{gamma} ratio of about 70:30 (slightly less in (AgI)0.8- (NaPO3)0.2). At 453, 523 and 623 deg. K the crystalline material is mainly {alpha}AgI. Crystalline 16-silver dodecaiodide diphosphate (Ag16I12P2O7) is also present between 373 and 523 deg. K at a 5-10% level. It disappears at 623-bar K because the crystal melts.

  7. Conceptual Commitments of AGI Systems: Editorial, Commentaries, and Response

    NASA Astrophysics Data System (ADS)

    2013-06-01

    Editorial: Conceptual Commitments of AGI Systems Haris Dindo / James Marshall / Giovanni Pezzulo 23 General Problems of Unified Theories of Cognition, and Another Conceptual Commitment of LIDA Benjamin Angerer / Stefan Schneider 26 LIDA, Committed to Consciousness Antonio Chella 28 The Radical Interactionism Conceptual Commitment Olivier L. Georgeon / David W. Aha 31 Commitments of the Soar Cognitive Architecture John E. Laird 36 Conceptual Commitments of AGI Projects Pei Wang 39 Will (dis)Embodied LIDA Agents be Socially Interactive? Travis J. Wiltshire / Emilio J. C. Lobato / Florian G. Jentsch / Stephen M. Fiore 42 Author's Response to Commentaries Steve Strain / Stan Franklin 48

  8. Application of Gaia Analysis Software AGIS to Nano-JASMINE

    NASA Astrophysics Data System (ADS)

    Yamada, Y.; Lammers, U.; Gouda, N.

    2011-07-01

    The core data reduction for the Nano-JASMINE mission is planned to be done with Gaia's Astrometric Global Iterative Solution (AGIS). Nano-JASMINE is an ultra small (35 kg) satellite for astrometry observations in Japan and Gaia is ESA's large (over 1000 kg) next-generation astrometry mission. The accuracy of Nano-JASMINE is about 3 mas, comparable to the Hipparcos mission, Gaia's predecessor some 20 years ago. It is challenging that such a small satellite can perform real scientific observations. The collaboration for sharing software started in 2007. In addition to similar design and operating principles of the two missions, this is possible thanks to the encapsulation of all Gaia-specific aspects of AGIS in a Parameter Database. Nano-JASMINE will be the test bench for the Gaia AGIS software. We present this idea in detail and the necessary practical steps to make AGIS work with Nano-JASMINE data. We also show the key mission parameters, goals, and status of the data reduction for the Nano-JASMINE.

  9. Electrochemical reclamation of silver from silver-plating wastewater using static cylinder electrodes and a pulsed electric field.

    PubMed

    Su, Yuan-Bo; Li, Qing-Biao; Wang, Yuan-Peng; Wang, Hai-Tao; Huang, Jia-le; Yang, Xin

    2009-10-30

    Silver was reclaimed from silver-plating wastewater by using a pulsed electric field (PEF) combined with static cylinder electrodes (SCE). The conditions that produced the maximal silver recovery rate (RR(Ag)) (99%) were as follows: average retention time of 10 min, interelectrode gap of 50mm, solution pH of 9.0, temperature of 45 degrees C, initial Ag(I) concentration of 1000 mg L(-1), PEF pulse frequency of 1200 Hz, current density of 5.0 A m(-2) and a pulse duty cycle of 60%. Compared with the conventional direct current (DC) technology, the PEF process exhibited improvements in the silver recovery rate (RR(Ag)), total energy consumption (TEC) and physical properties of the silver deposits, especially for low Ag(I) concentrations, for example, from 500 to 1000 mg L(-1). For an initial Ag(I) concentration of 500 mg L(-1), the PEF process produced an RR(Ag) of up to 99%, and the TEC was 4.56 kWh (kg Ag)(-1). In comparison, the RR(Ag) and TEC were 90% and 5.66 kWh (kg Ag)(-1), respectively, in the DC process. The results of SEM observation and XRD analysis indicated that the silver deposits formed by the PEF process were smaller, denser, and of a higher purity than those produced by the DC process. Therefore, the presented method was effective for reclaiming silver from silver-plating wastewater. PMID:19545945

  10. Formation of Nanoscale Elemental Silver Particles via Enzymatic Reduction by Geobacter sulfurreducens▿

    PubMed Central

    Law, Nicholas; Ansari, Saadia; Livens, Francis R.; Renshaw, Joanna C.; Lloyd, Jonathan R.

    2008-01-01

    Geobacter sulfurreducens reduced Ag(I) (as insoluble AgCl or Ag+ ions), via a mechanism involving c-type cytochromes, precipitating extracellular nanoscale Ag(0). These results extend the range of metals known to be reduced by Geobacter species and offer a method for recovering silver from contaminated water as potentially useful silver nanoparticles. PMID:18723646

  11. Toward full spectrum speciation of silver nanoparticles and ionic silver by on-line coupling of hollow fiber flow field-flow fractionation and minicolumn concentration with multiple detectors.

    PubMed

    Tan, Zhi-Qiang; Liu, Jing-Fu; Guo, Xiao-Ru; Yin, Yong-Guang; Byeon, Seul Kee; Moon, Myeong Hee; Jiang, Gui-Bin

    2015-08-18

    The intertransformation of silver nanoparticles (AgNPs) and ionic silver (Ag(I)) in the environment determines their transport, uptake, and toxicity, demanding methods to simultaneously separate and quantify AgNPs and Ag(I). For the first time, hollow fiber flow field-flow fractionation (HF5) and minicolumn concentration were on-line coupled together with multiple detectors (including UV-vis spectrometry, dynamic light scattering, and inductively coupled plasma mass spectrometry) for full spectrum separation, characterization, and quantification of various Ag(I) species (i.e., free Ag(I), weak and strong Ag(I) complexes) and differently sized AgNPs. While HF5 was employed for filtration and fractionation of AgNPs (>2 nm), the minicolumn packed with Amberlite IR120 resin functioned to trap free Ag(I) or weak Ag(I) complexes coming from the radial flow of HF5 together with the strong Ag(I) complexes and tiny AgNPs (<2 nm), which were further discriminated in a second run of focusing by oxidizing >90% of tiny AgNPs to free Ag(I) and trapped in the minicolumn. The excellent performance was verified by the good agreement of the characterization results of AgNPs determined by this method with that by transmission electron microscopy, and the satisfactory recoveries (70.7-108%) for seven Ag species, including Ag(I), the adduct of Ag(I) and cysteine, and five AgNPs with nominal diameters of 1.4 nm, 10 nm, 20 nm, 40 nm, and 60 nm in surface water samples. PMID:26222150

  12. Silver-Mordenite for Radiologic Gas Capture from Complex Streams: Dual Catalytic CH3I Decomposition and I Confinement

    SciTech Connect

    Tina M. Nenoff; Mark Rodriguez; Nick Soelberg; Karena W. Chapman

    2014-12-01

    The effective capture and storage of radiological iodine (129I) remains a strong concern for safe nuclear waste storage and safe nuclear energy. Silver-containing mordenite (MOR) is a longstanding benchmark for iodine capture. In nuclear fuel reprocessing scenarios, complex gas streams will be present and the need for high selectivity of all iodine containing compounds is of the utmost importance for safety and the environment. In particular, a molecular level understanding of the sorption of organic iodine compounds is not well understood. Here we probe the structure and distribution of methyl iodide sorbed by silver-containing MOR using a combination of crystallographic and materials characterization techniques including: infrared spectroscopy, thermogravimetric analysis with mass spectrometry, Micro-X-ray Fluorescence, powder X-ray diffraction analysis, and pair distribution function analysis. The iodine is captured inside the MOR pore in the form of AgI nanoparticles, that is consistent with the pores sizes of the MOR, indicating that the molecule is both physically and chemically captured in the Ag-MOR. The organic component is surface catalyzed by the zeolite via the formation of Surface Methoxy Species (SMS) that result in downstream organics of dimethyl ether and methanol formation.

  13. Taming the Reactivity of Glycosyl Iodides To Achieve Stereoselective Glycosidation.

    PubMed

    Gervay-Hague, Jacquelyn

    2016-01-19

    that even highly functionalized aglycon acceptors add. Following the coupling event, the TMS ethers are readily removed by methanolysis, and since all of the byproducts are volatile, multiple reactions can be performed in a single reaction vessel without isolation of intermediates. In this fashion, per-O-TMS monosaccharides can be converted to biologically relevant α-linked glycolipids in one pot. The stereochemical outcome of these reactions can also be switched to β-glycoside formation by addition of silver to chelate the iodide, thus favoring SN2 displacement of the α-iodide. While iodides derived from benzyl and silyl ether-protected oligosaccharides are susceptible to interglycosidic bond cleavage when treated with TMSI, the introduction of a single acetate protecting group prevents this unwanted side reaction. Partial acetylation of armed glycosyl iodides also attenuates HI elimination side reactions. Conversely, fully acetylated glycosyl iodides are deactivated and require metal catalysis in order for glycosidation to occur. Recent findings indicate that I2 activation of per-O-acetylated mono-, di-, and trisaccharides promotes glycosidation of cyclic ethers to give β-linked iodoalkyl glycoconjugates in one step. Products of these reactions have been converted into multivalent carbohydrate displays. With these synthetic pathways elucidated, chemical reactivity can be exquisitely controlled by the judicious selection of protecting groups to achieve high stereocontrol in step-economical processes. PMID:26524481

  14. Mercury iodide crystal growth

    NASA Technical Reports Server (NTRS)

    Cadoret, R.

    1982-01-01

    The purpose of the Mercury Iodide Crystal Growth (MICG) experiment is the growth of near-perfect single crystals of mercury Iodide (HgI2) in a microgravity environment which will decrease the convection effects on crystal growth. Evaporation and condensation are the only transformations involved in this experiment. To accomplish these objectives, a two-zone furnace will be used in which two sensors collect the temperature data (one in each zone).

  15. Chemoselective allene aziridination via Ag(I) catalysis.

    PubMed

    Rigoli, Jared W; Weatherly, Cale D; Vo, Brian T; Neale, Samuel; Meis, Alan R; Schomaker, Jennifer M

    2013-01-18

    Allene aziridination generates useful bicyclic methylene aziridine scaffolds that can be flexibly transformed into a range of stereochemically complex and densely functionalized amine-containing stereotriads. The scope of this chemistry has been limited by the poor chemoselectivity that often results when typical dinuclear Rh(II) catalysts are employed with homoallenic carbamates. Herein, Ag(I) catalysts that significantly improve the scope and yield of bicyclic methylene aziridines that can be prepared via allene aziridination are described. PMID:23265391

  16. Chemoselective Allene Aziridination via Ag(I) Catalysis

    PubMed Central

    Rigoli, Jared W.; Weatherly, Cale D.; Vo, Brian T.; Neale, Samuel; Meis, Alan R.

    2015-01-01

    Allene aziridination generates useful bicyclic methylene aziridine scaffolds that can be flexibly transformed into a range of stereochemically complex and densely functionalized amine-containing stereotriads. The scope of this chemistry has been limited by the poor chemoselectivity that often results when typical dinuclear Rh(II) catalysts are employed with homoallenic carbamates. Herein, Ag(I) catalysts that significantly improve the scope and yield of bicyclic methylene aziridines that can be prepared via allene aziridination are described. PMID:23265391

  17. Silver(I) Antimicrobial Cotton Nonwovens and Printcloth

    Technology Transfer Automated Retrieval System (TEKTRAN)

    In this paper we discuss the preparation and comparative evaluation of silver (I) [Ag(I)] nonwoven and woven antimicrobial barrier fabrics generated from commercial calcium-sodium alginates and laboratory prepared sodium carboxymethyl (CM) cotton nonwovens and CM-cotton printcloth for potential use ...

  18. Silver-catalysed protodecarboxylation of ortho-substituted benzoic acids.

    PubMed

    Cornella, Josep; Sanchez, Carolina; Banawa, David; Larrosa, Igor

    2009-12-14

    Catalytic amounts of Ag(I) salts in DMSO have been found to promote the protodecarboxylation of a wide variety of ortho-substituted benzoic acids under mild conditions and in excellent yields, highlighting a possible role for silver in decarboxylative cross-couplings. PMID:19921021

  19. Introduction of extrinsic defects into mercuric iodide during processing

    NASA Astrophysics Data System (ADS)

    Hung, C.-Y.; Bao, X. J.; Schlesinger, T. E.; James, R. B.; Cheng, A. Y.; Ortale, C.; van den Berg, L.

    1993-05-01

    Low-temperature photoluminescence spectroscopy (PL) measurements were performed on mercuric iodide (HgI2) crystals which were intentionally doped with copper or silver during KI etching. PL spectra obtained after these doping experiments show specific Cu and Ag features similar to those previously observed after deposition of Cu or Ag contacts on mercuric iodide crystals. The in-diffusion of Cu or Ag into bulk HgI2 has also been confirmed a few days after doping. This diffusion introduces new recombination centers in the material. This work suggests that the processing steps used to fabricate mercuric iodide nuclear detectors can lead to the introduction of new defects which are detrimental to detector performance.

  20. AGIS: Evolution of Distributed Computing information system for ATLAS

    NASA Astrophysics Data System (ADS)

    Anisenkov, A.; Di Girolamo, A.; Alandes, M.; Karavakis, E.

    2015-12-01

    ATLAS, a particle physics experiment at the Large Hadron Collider at CERN, produces petabytes of data annually through simulation production and tens of petabytes of data per year from the detector itself. The ATLAS computing model embraces the Grid paradigm and a high degree of decentralization of computing resources in order to meet the ATLAS requirements of petabytes scale data operations. It has been evolved after the first period of LHC data taking (Run-1) in order to cope with new challenges of the upcoming Run- 2. In this paper we describe the evolution and recent developments of the ATLAS Grid Information System (AGIS), developed in order to integrate configuration and status information about resources, services and topology of the computing infrastructure used by the ATLAS Distributed Computing applications and services.

  1. Speciation Analysis of Labile and Total Silver(I) in Nanosilver Dispersions and Environmental Waters by Hollow Fiber Supported Liquid Membrane Extraction.

    PubMed

    Chao, Jing-Bo; Zhou, Xiao-Xia; Shen, Mo-Hai; Tan, Zhi-Qiang; Liu, Rui; Yu, Su-Juan; Wang, Xiao-Wei; Liu, Jing-Fu

    2015-12-15

    Hollow fiber supported liquid membrane (HFSLM) extraction was coupled with ICP-MS for speciation analysis of labile Ag(I) and total Ag(I) in dispersions of silver nanoparticles (AgNPs) and environmental waters. Ag(I) in aqueous samples was extracted into the HFSLM of 5%(m/v) tri-n-octylphosphine oxide in n-undecane, and stripped in the acceptor of 10 mM Na2S2O3 and 1 mM Cu(NO3)2 prepared in 5 mM NaH2PO4-Na2HPO4 buffer (pH 7.5). Negligible depletion and exhaustive extraction were conducted under static and 250 rpm shaking to extract the labile Ag(I) and total Ag(I), respectively. The extraction equilibration was reached in 8 h for both extraction modes. The extraction efficiency and detection limit were (2.97 ± 0.25)% and 0.1 μg/L for labile Ag(I), and (82.3 ± 2.0)% and 0.5 μg/L for total Ag(I) detection, respectively. The proposed method was applied to determine labile Ag(I) and total Ag(I) in different sized AgNP dispersions and real environmental waters, with spiked recoveries of total Ag(I) in the range of 74.0-98.1%. With the capability of distinguishing labile and total Ag(I), our method offers a new approach for evaluating the bioavailability and understanding the fate and toxicity of AgNPs in aquatic systems. PMID:26580982

  2. Frequently Asked Questions on Potassium Iodide (KI)

    MedlinePlus

    ... needs to take potassium iodide (KI) after a nuclear radiation release? What potassium iodide (KI) products are currently ... needs to take potassium iodide (KI) after a nuclear radiation release? The FDA guidance prioritizes groups based on ...

  3. Detection of Radiation Tracks Recorded on Silver-Salt Photographic Materials by Fluorescence-Labeling Method

    NASA Astrophysics Data System (ADS)

    Kuge, Ken'ichi; Inoue, Ryouhei; Oishi, Yasushi; Yasuda, Nakahiro; Kodaira, Satoshi; Sato, Osamu

    2013-10-01

    We have proposed a new fluorescence-labeling method to detect radiation tracks recorded on silver-salt photographic materials. Fluorescence images of tracks were obtained by converting the developed silver to silver iodide as a mordant by bleaching and selectively adsorbing a fluorescent dye, namely, 3,3'-diethyl-2,2'-oxacyanine iodide, on it. The dye emitted blue and green fluorescent lights in the adsorbed state to silver iodide. Even tracks masked with fake particles could be recognized clearly in the fluorescence images, because the dye was adsorbed only on silver iodide. This new fluorescence-labeling method will facilitate the development of new technologies for the analysis of radiation tracks on the basis of the color information obtained from the tracks.

  4. Hydrogen iodide decomposition

    DOEpatents

    O'Keefe, Dennis R.; Norman, John H.

    1983-01-01

    Liquid hydrogen iodide is decomposed to form hydrogen and iodine in the presence of water using a soluble catalyst. Decomposition is carried out at a temperature between about 350.degree. K. and about 525.degree. K. and at a corresponding pressure between about 25 and about 300 atmospheres in the presence of an aqueous solution which acts as a carrier for the homogeneous catalyst. Various halides of the platinum group metals, particularly Pd, Rh and Pt, are used, particularly the chlorides and iodides which exhibit good solubility. After separation of the H.sub.2, the stream from the decomposer is countercurrently extracted with nearly dry HI to remove I.sub.2. The wet phase contains most of the catalyst and is recycled directly to the decomposition step. The catalyst in the remaining almost dry HI-I.sub.2 phase is then extracted into a wet phase which is also recycled. The catalyst-free HI-I.sub.2 phase is finally distilled to separate the HI and I.sub.2. The HI is recycled to the reactor; the I.sub.2 is returned to a reactor operating in accordance with the Bunsen equation to create more HI.

  5. The Advanced Gamma-Ray Imaging System (AGIS): Science Highlights

    SciTech Connect

    Buckley, J.; Coppi, P.; Digel, S.; Funk, S.; Krawczynski, H.; Krennrich, F.; Pohl, M.; Romani, R.; Vassiliev, V.; /UCLA

    2011-11-21

    The Advanced Gamma-ray Imaging System (AGIS), a future gamma-ray telescope consisting of an array of {approx}50 atmospheric Cherenkov telescopes distributed over an area of {approx}1 km{sup 2}, will provide a powerful new tool for exploring the high-energy universe. The order-of-magnitude increase in sensitivity and improved angular resolution could provide the first detailed images of {gamma}-ray emission from other nearby galaxies or galaxy clusters. The large effective area will provide unprecedented sensitivity to short transients (such as flares from AGNs and GRBs) probing both intrinsic spectral variability (revealing the details of the acceleration mechanism and geometry) as well as constraining the high-energy dispersion in the velocity of light (probing the structure of spacetime and Lorentz invariance). A wide field of view ({approx}4 times that of current instruments) and excellent angular resolution (several times better than current instruments) will allow for an unprecedented survey of the Galactic plane, providing a deep unobscured survey of SNRs, X-ray binaries, pulsar-wind nebulae, molecular cloud complexes and other sources. The differential flux sensitivity of {approx}10{sup -13} erg cm{sup -2} sec{sup -1} will rival the most sensitive X-ray instruments for these extended Galactic sources. The excellent capabilities of AGIS at energies below 100 GeV will provide sensitivity to AGN and GRBs out to cosmological redshifts, increasing the number of AGNs detected at high energies from about 20 to more than 100, permitting population studies that will provide valuable insights into both a unified model for AGN and a detailed measurement of the effects of intergalactic absorption from the diffuse extragalactic background light. A new instrument with fast-slewing wide-field telescopes could provide detections of a number of long-duration GRBs providing important physical constraints from this new spectral component. The new array will also have excellent

  6. Nano-JASMINE: use of AGIS for the next astrometric satellite

    NASA Astrophysics Data System (ADS)

    Yamada, Y.; Gouda, N.; Lammers, U.

    2011-02-01

    The core data reduction for the Nano-JASMINE mission is planned to be done with Gaia's Astrometric Global Iterative Solution (AGIS). The collaboration started at 2007 prompted by Uwe Lammers' proposal. In addition to similar design and operating principles of the two missions, this is possible thanks to the encapsulation of all Gaia-specific aspects of AGIS in a Parameter Database. Nano-JASMINE will be the test bench for Gaia AGIS software. We present this idea in detail and the necessary practical steps to make AGIS work with Nano-JASMINE data. We also show the key mission parameters, goals, and status of the data reduction for the Nano-JASMINE.

  7. Civil aircraft vortex wake. TsAGI's research activities

    NASA Astrophysics Data System (ADS)

    Chernyshev, S. L.; Gaifullin, A. M.; Sviridenko, Yu. N.

    2014-11-01

    This paper provides a review of research conducted in TsAGI (Central AeroHydrodynamic Institute) concerning a vortex wake behind an airliner. The research into this area of theoretical and practical importance have been done both in Russia and in other countries, for which these studies became a vital necessity at the end of the 20th century. The paper describes the main methods and ratios on which software systems used to calculate the evolution of a vortex wake in a turbulent atmosphere are based. Verification of calculation results proved their acceptable consistency with the known experimental data. The mechanism of circulation loss in a vortex wake which is based on the analytical solution for the problem of two vortices diffusing in a viscous fluid is also described. The paper also describes the model of behavior of an aircraft which has deliberately or unintentionally entered a vortex wake behind another aircraft. Approximated results of calculations performed according to this model by means of artificial neural networks enabled the researchers to model the dynamics of an aircraft in a vortex wake on flight simulators on-line.

  8. Antibacterial, antifungal, phytotoxic, and genotoxic properties of two complexes of Ag(I) with sulfachloropyridazine (SCP): X-ray diffraction of [Ag(SCP)]n.

    PubMed

    Mosconi, Natalia; Giulidori, Cecilia; Velluti, Francesca; Hure, Estela; Postigo, Agustina; Borthagaray, Graciela; Back, Davi Fernando; Torre, María H; Rizzotto, Marcela

    2014-06-01

    We report the synthesis, characterization, antibacterial and antifungal activities, phytotoxicity, and genotoxicity of two new complexes of silver(I) with sulfachloropyridazine (SCP), one of which is heteroleptic with SCP and SCN(-) ligands (Ag-SCP-SCN), the other of which is homoleptic (Ag-SCP); furthermore, the crystal structure of the homoleptic complex is disclosed. The heterocyclic N atom nearest to the Cl atom and the N(sulfonamide) atom could be coordination sites for the silver ion in the Ag-SCP-SCN complex. The Ag-SCP complex is a polymeric compound with metal-metal bonds, and the heterocyclic and sulfonamide N atoms are points of coordination for Ag(I) . Both complexes showed activity against all the tested bacteria, and in the cases of Escherichia coli and Pseudomonas aeruginosa, the action was better than that of SCP. In all cases, both silver-SCP complexes showed better antifungal activity than SCP, which was inactive against the tested fungi. Notably, the activity against P. aeruginosa, a nosocomial multidrug-resistant pathogen, was better than that of the reference antibiotic cefotaxim. Both silver-sulfa complexes displayed moderate activity against the tested yeast, especially for C. neoformans, which is an important fact considering the incidence of cryptococcosis, mainly in immune-deficient patients. No chromosomal aberrations were observed with the Allium cepa test, which is auspicious for further study of these complexes as potential drugs. PMID:24806993

  9. Etching of mercuric iodide in cation iodide solutions

    NASA Astrophysics Data System (ADS)

    Ponpon, J. P.; Amann, M.

    2006-07-01

    The surface properties of mercuric iodide after etching in various cation iodide solutions have been investigated in terms of dissolution rate, morphology, electrical properties and reaction with water vapour. No significant differences have been observed in the etching rates. However, dissolution of HgI 2 in NH 4I, NaI, KI or RbI leaves the surface more or less covered with a residual iodo mercurate compound whose electrical properties and stability with regard to humidity may noticeably influence the behaviour of mercuric iodide devices. The smallest effect has been observed for etching in NaI.

  10. Dielectric and conductivity relaxation in AgI doped silver selenite superionic glasses

    SciTech Connect

    Deb, B.; Ghosh, A.

    2010-10-15

    Non-Debye relaxation in superionic AgI-Ag{sub 2}O-SeO{sub 2} glasses has been investigated as a function of frequency and temperature. The experimental data have been analyzed in the framework of complex dielectric permittivity and complex electric modulus formalisms. The dielectric permittivity data have been well interpreted using the Havriliak-Negami function. The electric modulus data have been analyzed by invoking Kohlrausch-Williams-Watts function and various parameters describing the relaxation mechanism have been obtained. The temperature and compositional variation in relaxation times and the activation energy, obtained from dielectric permittivity as well as from electric modulus data, have been compared. The low value of stretched exponential parameter implies a highly nonexponential nature of relaxation and is attributed to the correlated ionic motion. The values of the stretched exponential parameter are observed to be independent of temperature as well as composition. Different scaling formalisms have been applied to understand the temperature and compositional dependence of the relaxation mechanism. The scaling of dielectric loss spectra and electric modulus spectra results in master curves, which signifies that the relaxation mechanism is independent of temperature as well as composition.

  11. Photoinduced silver nanoparticles/nanorings on plasmid DNA scaffolds.

    PubMed

    Liu, Jianhua; Zhang, Xiaoliang; Yu, Mei; Li, Songmei; Zhang, Jindan

    2012-01-23

    Biological scaffolds are being actively explored for the synthesis of nanomaterials with novel structures and unexpected properties. Toroidal plasmid DNA separated from the Bacillus host is applied as a sacrificial mold for the synthesis of silver nanoparticles and nanorings. The photoirradiation method is applied to reduce Ag(I) on the plasmid. The nanoparticles are obtained by varying the concentration of the Ag(I) ion solution and the exposure time of the plasmid-Ag(I) complex under UV light at 254 nm and room temperature. It is found that the plasmid serves not only as a template but also as a reductant to drive the silver nucleation and deposition. The resulting nanoparticles have a face-centered cubic (fcc) crystal structure and 20-30 nm average diameter. The detailed mechanism is discussed, and other metals or alloys could also be synthesized with this method. PMID:22102552

  12. 21 CFR 172.375 - Potassium iodide.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false 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...

  13. 21 CFR 172.375 - Potassium iodide.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false 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...

  14. 21 CFR 172.375 - Potassium iodide.

    Code of Federal Regulations, 2010 CFR

    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...

  15. 21 CFR 172.375 - Potassium iodide.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Potassium iodide. 172.375 Section 172.375 Food and....375 Potassium iodide. The food additive potassium iodide may be safely used in accordance with the following prescribed conditions: (a) Potassium iodide may be safely added to a food as a source of...

  16. 21 CFR 172.375 - Potassium iodide.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false 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...

  17. Excited State Electronic Properties of Sodium Iodide and Cesium Iodide

    SciTech Connect

    Campbell, Luke W.; Gao, Fei

    2013-05-01

    We compute from first principles the dielectric function, loss function, lifetime and scattering rate of quasiparticles due to electronic losses, and secondary particle spectrum due to plasmon decay in two scintillating alkali halides, sodium iodide and cesium iodide. Particular emphasis is placed on quasiparticles within several multiples of the band gap from the band edges. A theory for the decay spectra of plasmons and other electronic excitations in crystals is presented. Applications to Monte Carlo radiation transport codes are discussed.

  18. Silver-109 NMR spectroscopy of inorganic solids.

    PubMed

    Penner, Glenn H; Li, Wenli

    2004-09-01

    In this study the (109)Ag NMR spectra of the following solid inorganic silver-containing compounds were investigated: AgNO(3), AgNO(2), Ag(2)SO(4), Ag(2)SO(3), AgCO(3), Ag(3)PO(4), AgCl, AgBr, AgI, AgSO(3)CH(3), silver p-toluenesulfonate, NaAg(CN)(2), KAg(CN)(2), K(3)Ag(CN)(4), Me(4)NAgCl(2), silver diethylthiocarbamate, silver lactate, silver acetate, silver citrate, and bis[(N,N(1)-di-tert-butylformamidinato)silver(I)]. The magic angle spinning (MAS) spectra of all compounds were obtained. In some cases, when protons were available, the (1)H to (109)Ag cross-polarization (CP) technique was used to enhance the signal and shorten the experimental relaxation delay. It was possible to obtain slow MAS (or CP/MAS) or nonspinning spectra for 10 samples, allowing the determination of the principal components of the (109)Ag chemical shift (CS) tensors. The isotropic chemical shifts and the CS tensors are discussed in light of the available crystal structures. The need for an accepted standard for referencing (109)Ag chemical shifts and the use of AgSO(3)CH(3) as a CP setup sample are also discussed. PMID:15332810

  19. Silver Sulfadiazine

    MedlinePlus

    Silver sulfadiazine, a sulfa drug, is used to prevent and treat infections of second- and third-degree ... Silver sulfadiazine comes in a cream. Silver sulfadiazine usually is applied once or twice a day. Follow ...

  20. The AGI-ASU-NASA Triad Program for K-12 Earth and Space Science Education

    NASA Astrophysics Data System (ADS)

    Pacheco, H. A.; Semken, S. C.; Taylor, W.; Benbow, A. E.

    2011-12-01

    The NASA Triad program of the American Geological Institute (AGI) and Arizona State University School of Earth and Space Exploration (ASU SESE) is a three-part effort to promote Earth and space science literacy and STEM education at the national level, funded by NASA through a cooperative agreement starting in 2010. NASA Triad comprises (1) infusion of NASA STEM content into AGI's secondary Earth science curricula; (2) national lead teacher professional development workshops; and (3) an online professional development guide for teachers running NASA STEM workshops. The Triad collaboration draws on AGI's inquiry-based curriculum and teacher professional-development resources and workforce-building programs; ASU SESE's spectrum of research in Mars and Moon exploration, astrobiology, meteoritics, Earth systems, and cyberlearning; and direct access to NASA facilities and dynamic education resources. Triad milestones to date include integration of NASA resources into AGI's print and online curricula and two week-long, national-scale, teacher-leader professional development academies in Earth and space sciences presented at ASU Dietz Museum in Tempe and NASA Johnson Space Flight Center in Houston. Robust front-end and formative assessments of these program components, including content gains, teacher-perceived classroom relevance, teacher-cohort lesson development, and teacher workshop design, have been conducted. Quantitative and qualitative findings from these assessment activities have been applied to identify best and most effective practices, which will be disseminated nationally and globally through AGI and NASA channels.

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

    SciTech Connect

    Soelberg, Nicholas Ray; Watson, Tony Leroy

    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.

  2. The Advanced Gamma-ray Imaging System (AGIS) Telescope Optical System Designs

    SciTech Connect

    Bugaev, V.; Buckley, J.; Krawczynski, H.; Diegel, S.; Romani, R.; Falcone, A.; Fegan, S.; Vassiliev, V.; Finley, J.; Guarino, V.; Hanna, D.; Kaaret, P.; Konopelko, A.; Ramsey, B.; Weekes, T.

    2008-12-24

    AGIS is a conceptual design for a future ground-based gamma-ray observatory operating in the energy range 25 GeV-100 TeV, which is based on an array of {approx}20-100 imaging atmospheric Cherenkov telescopes (IACTs). The desired improvement in sensitivity, angular resolution, and reliability of operation of AGIS imposes demanding technological and cost requirements on the design of the IACTs. We are considering several options for the optical system (OS) of the AGIS telescopes, which include the traditional Davies-Cotton design as well as novel two-mirror design. Emerging mirror production technologies based on replication processes such as cold and hot glass slumping, cured carbon fiber reinforced plastic (CFRP), and electroforming provide new opportunities for cost-effective solutions for the design of the OS.

  3. Immobilization of radioactive iodine in silver aluminophosphate glasses.

    PubMed

    Lemesle, Thomas; Méar, François O; Campayo, Lionel; Pinet, Olivier; Revel, Bertrand; Montagne, Lionel

    2014-01-15

    Silver aluminophosphate glasses have been investigated as matrices for the immobilization of radioactive iodine. In this study, up to 28mol% AgI have been incorporated without volatilization thanks to a low temperature synthesis protocol. Alumina was added in the composition in order to increase the glass transition temperature for a better thermal stability in a repository conditions. Two series of glasses have been investigated, based on AgPO3 and Ag5P3O10 compositions, and with 0-5mol% Al2O3. We report (31)P, (27)Al and (109)Ag NMR study of these glasses, including advanced measurement of the connectivities through {(27)Al}-(31)P cross-polarization and (31)P-(31)P double-quantum correlation. We confirm that AgI is inserted in the aluminophosphate glasses and does not form clusters. AgI does not induce any modification of the glass polymerization but only an expansion of the network. Despite no evidence for crystallization could be obtained from XRD, NMR revealed that the introduction of AgI induces an exclusion of alumina from the network, leading to the crystallization of aluminophosphate phases such as Al(PO3)3 or AlPO4. As a consequence, despite NMR gives evidence for the presence of aluminophosphate bonds, only a limited effect of alumina addition on thermal properties is observed. PMID:24295764

  4. Developing an Ethical Framework for All Geoscientists: AGI Guidelines for Ethical Professional Conduct

    NASA Astrophysics Data System (ADS)

    Boland, Maeve A.; Leahy, P. Patrick; Keane, Christopher M.

    2016-04-01

    In 1997, a group of geoscientists and others recognized the need for a broad-based set of ethical standards for the geosciences that would be an expression of the highest common denominator of values for the profession. The American Geosciences Institute (AGI) coordinated the development of the 1999 AGI Guidelines for Ethical Professional Conduct and their subsequent revision in 2015. AGI is a nonprofit federation of 51 geoscientific and professional organizations that span the geosciences and have approximately 250,000 members. AGI serves as a voice for shared interests in the geoscience community and one of its roles is to facilitate collaboration and discussion among its member societies on matters of common or overarching concern. In this capacity, AGI convened a working group to create the 1999 Guidelines for Ethical Professional Conduct and a further working group to revise the Guidelines in 2015 through a consensus process involving all member societies. The Guidelines are an aspirational document, setting out ideals and high levels of achievement for the profession. They have no provision for disciplinary of enforcement action and they do not supersede the ethics statements or codes of any member society. The 1999 Guidelines pay considerable attention to the professional behavior of geoscientists. The 2015 Guidelines place greater emphasis on the societal context of the geosciences and the responsibilities of geoscientists in areas such as communication, education, and the challenges of understanding complex natural systems. The 2015 Guidelines have been endorsed by 29 member societies to date. To translate the aspirations in the Guidelines into specific actions, AGI has facilitated discussions on the practical implications of aspects of the Guidelines. One outcome of these discussions has been a Consensus Statement Regarding Access and Inclusion of Individuals Living with Disabilities in the Geosciences.

  5. Digermylene Oxide Stabilized Group 11 Metal Iodide Complexes.

    PubMed

    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

  6. A metal-organic framework with immobilized Ag(i) for highly efficient desulfurization of liquid fuels.

    PubMed

    Huang, Minhui; Chang, Ganggang; Su, Ye; Xing, Huabin; Zhang, Zhiguo; Yang, Yiwen; Ren, Qilong; Bao, Zongbi; Chen, Banglin

    2015-08-01

    A metal-organic framework immobilized with Ag(i) sites, namely, (Cr)-MIL-101-SO3Ag, was successfully developed as a highly efficient desulfurization adsorbent because of the strong binding of these Ag(i) sites for thiophene derivatives. PMID:26136210

  7. IODIDE DEFICIENCY, THYROID HORMONES, AND NEURODEVELOPMENT

    EPA Science Inventory

    ABSTRACT BODY: Iodide is an essential nutrient for thyroid hormone synthesis. Severe iodide insufficiency during early development is associated with cognitive deficits. Environmental contaminants can perturb the thyroid axis and this perturbation may be more acute under conditio...

  8. 21 CFR 582.5634 - Potassium iodide.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 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....

  9. 21 CFR 582.5634 - Potassium iodide.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 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....

  10. 21 CFR 184.1634 - Potassium iodide.

    Code of Federal Regulations, 2010 CFR

    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...

  11. 21 CFR 184.1634 - Potassium iodide.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Potassium iodide. 184.1634 Section 184.1634 Food... GRAS § 184.1634 Potassium iodide. (a) Potassium iodide (KI, CAS Reg. No. 7681-11-0) is the potassium... reacting hydriodic acid (HI) with potassium bicarbonate (KHCO3). (b) The ingredient meets...

  12. 21 CFR 582.5634 - Potassium iodide.

    Code of Federal Regulations, 2010 CFR

    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....

  13. 21 CFR 582.5634 - Potassium iodide.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 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....

  14. 21 CFR 184.1634 - Potassium iodide.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false 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...

  15. 21 CFR 582.5634 - Potassium iodide.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 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....

  16. 21 CFR 184.1634 - Potassium iodide.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false 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...

  17. 21 CFR 184.1634 - Potassium iodide.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false 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...

  18. Catalytic oxidation of butyl acetate over silver-loaded zeolites.

    PubMed

    Wong, Cheng Teng; Abdullah, Ahmad Zuhairi; Bhatia, Subhash

    2008-09-15

    The performance of silver-loaded zeolite (HY and HZSM-5) catalysts in the oxidation of butyl acetate as a model volatile organic compound (VOC) was studied. The objective was to find a catalyst with superior activity, selectivity towards deep oxidation product and stability. The catalyst activity was measured under excess oxygen condition in a packed bed reactor operated at gas hourly space velocity (GHSV)=15,000-32,000 h(-1), reaction temperature between 150 and 500 degrees C and butyl acetate inlet concentration of 1000-4000 ppm. Both AgY and AgZSM-5 catalysts exhibited high activity in the oxidation of butyl acetate. Despite lower silver content, AgY showed better activity, attributed to better metal dispersion, surface characteristics and acidity, and its pore system. Total conversion of butyl acetate was achieved at above 400 degrees C. The oxidation of butyl acetate followed a simple power law model. The reaction orders, n and m were evaluated under differential mode by varying the VOC partial pressure between 0.004 and 0.018 atm and partial pressure of oxygen between 0.05 and 0.20 atm. The reaction rate was independent of oxygen concentration and single order with respect to VOC concentration. The activation energies were 19.78 kJ/mol for AgY and 32.26 kJ/mol for AgZSM-5, respectively. PMID:18294771

  19. Faster, Better, Cheaper: News on Seeking Gaia's Astrometric Solution with AGIS

    NASA Astrophysics Data System (ADS)

    Lammers, U.; Lindegren, L.; Bombrun, A.; O'Mullane, W.; Hobbs, D.

    2010-12-01

    Gaia is ESA’s ambitious space astrometry mission with a foreseen launch date in early 2012. Its main objective is to perform a stellar census of the 1000 Million brightest objects in our galaxy (completeness to V=20 mag) from which an astrometric catalog of micro-arcsec level accuracy will be constructed. A key element in this endeavor is the Astrometric Global Iterative Solution (AGIS) - the mathematical and numerical framework for combining the ≍80 available observations per star obtained during Gaia’s 5yr lifetime into a single global astrometric solution. At last year’s ADASS XVIII we presented (O4.1) in detail the fundamental working principles of AGIS, its development status, and selected results obtained by running the system on processing hardware at ESAC, Madrid with large-scale simulated data sets. We present here the latest developments around AGIS highlighting in particular a much improved algebraic solving method that has recently been implemented. This Conjugate Gradient scheme improves the convergence behavior in significant ways and leads to a solution of much higher scientific quality. We also report on a new collaboration aiming at processing the data from the future small Japanese astrometry mission Nano-Jasmine with AGIS.

  20. A Comparison of AgI and CO2 Seeding Effects in Alberta Cumulus Clouds.

    NASA Astrophysics Data System (ADS)

    English, Marianne; Marwitz, John D.

    1981-05-01

    Three convective clouds extending above a stratocumulus layer were identified as being seedable on one day and were then seeded in a random sequence with CO2 pellets, a placebo and droppable AgI flares. The radar and microphysical seeding effects were observed with the Alberta Hail Project S-band radar and with the University of Wyoming Queen Air aircraft. Distinct seeding effects were observed in both seeded clouds by both data systems. The CO2 seeded cloud developed a single curtain of precipitation particles 18 min after seeding which reached the ground 20 min after seeding and ceased precipitating 10 min later. The placebo cloud failed to develop any precipitation-sized particles or radar echo and dissipated after 30 min. The AgI seeded cloud developed its first echo 8 min after seeding near the threshold temperature for AgI (7°C), produced precipitation at the ground 20 min after seeding, and continued to develop a new echo near the 7°C level and precipitate for 1 h. A natural echoing storm which occurred nearby was examined by radar and found to develop and evolve in a manner quite unlike the seeded clouds. It is plausible that the AgI continued to generate ice crystals in such a manner as to first initiate and then prolong the lifetime of precipitation while the curtain of CO2 pellets failed to initiate more than a single precipitation curtain.

  1. Distinctive green recovery of silver species from modified cellulose: mechanism and spectroscopic studies.

    PubMed

    Dwivedi, Amarendra Dhar; Dubey, Shashi Prabha; Sillanpää, Mika; Liimatainen, Henrikki; Suopajärvi, Terhi; Niinimäki, Jouko; Kwon, Young-Nam; Lee, Changha

    2015-05-01

    The present study aimed to recover precious silver in order to identify the adsorption coupled reduction pathways that determine this process. A combination technique of adsorption and nanocrystallization was used to investigate the recovery of silver species from taurine-cellulose (T-DAC) samples. The non-synthetic route of nanocrystallization yielded spherical zero-valent silver sized ∼ 18 nm. Rate-controlling steps were modeled by adsorption parameters by the best fit of Langmuir capacity (55 mg/g), pseudo-second order curves, and exothermic chemical reactions. The T-DAC was an excellent sorbing phase for the treatment of silver-polluted waters over a broad range of pH (2.1-10.1) and varying ionic strengths (8.5-850 mM, as NaCl), which are the conditions often encountered in industrial and mining effluents. A good recovery of silver (40-65%) was also obtained in the presence of Cd(II), Co(II), Cr(VI), Ni(II), and As(V) at lower or equivalent concentrations with Ag(I), either from individually added metals or from all metal ions mixed together. Desorption was compared with a series of five eluents including complexing agents. In these experiments acidified thiourea yielded 86% desorption of Ag(I). Aqueous silver reduced to metallic silver on the surface of the T-DAC samples, which was confirmed by X-ray photo electron spectroscopy. PMID:25732618

  2. Effects of silver nanoparticles on human dermal fibroblasts and epidermal keratinocytes.

    PubMed

    Galandáková, A; Franková, J; Ambrožová, N; Habartová, K; Pivodová, V; Zálešák, B; Šafářová, K; Smékalová, M; Ulrichová, J

    2016-09-01

    Biomedical application of silver nanoparticles (AgNPs) has been rapidly increasing. Owing to their strong antimicrobial activity, AgNPs are used in dermatology in the treatment of wounds and burns. However, recent evidence for their cytotoxicity gives rise to safety concerns. This study was undertaken as a part of an ongoing programme in our laboratory to develop a topical agent for wound healing. Here, we investigated the potential toxicity of AgNPs using normal human dermal fibroblasts (NHDF) and normal human epidermal keratinocytes (NHEK) with the aim of comparing the effects of AgNPs and ionic silver (Ag-I). Besides the effect of AgNPs and Ag-I on cell viability, the inflammatory response and DNA damage in AgNPs and Ag-I-treated cells were examined. The results showed that Ag-I were significantly more toxic than AgNPs both on NHDF and NHEK. Non-cytotoxic concentrations of AgNPs and Ag-I did not induce DNA strand breaks and did not affect inflammatory markers, except for a transient increase in interleukin 6 levels in Ag-I-treated NHDF. The results showed that AgNPs are more suitable for the intended application as a topical agent for wound healing up to the concentration 25 µg/mL. PMID:26500221

  3. Electrodeposition of Epitaxial Lead Iodide and Conversion to Textured Methylammonium Lead Iodide Perovskite.

    PubMed

    Hill, James C; Koza, Jakub A; Switzer, Jay A

    2015-12-01

    Applications for lead iodide, such as lasing, luminescence, radiation detection, and as a precursor for methylammonium lead iodide perovskite photovoltaic cells, require highly ordered crystalline thin films. Here, an electrochemical synthesis route is introduced that yields textured and epitaxial films of lead iodide at room temperature by reducing molecular iodine to iodide ions in the presence of lead ions. Lead iodide grows with a [0001] fiber texture on polycrystalline substrates such as fluorine-doped tin oxide. On single-crystal Au(100), Au(111), and Au(110) the out-of-plane orientation of lead iodide is also [0001], but the in-plane orientation is controlled by the single-crystal substrate. The epitaxial lead iodide on single-crystal gold is converted to textured methylammonium lead iodide perovskite with a preferred [110] orientation via methylammonium iodide vapor-assisted chemical transformation of the solid. PMID:26565593

  4. Iodide uptake by negatively charged clay interlayers?

    PubMed

    Miller, Andrew; Kruichak, Jessica; Mills, Melissa; Wang, Yifeng

    2015-09-01

    Understanding iodide interactions with clay minerals is critical to quantifying risk associated with nuclear waste disposal. Current thought assumes that iodide does not interact directly with clay minerals due to electrical repulsion between the iodide and the negatively charged clay layers. However, a growing body of work indicates a weak interaction between iodide and clays. The goal of this contribution is to report a conceptual model for iodide interaction with clays by considering clay mineral structures and emergent behaviors of chemical species in confined spaces. To approach the problem, a suite of clay minerals was used with varying degrees of isomorphic substitution, chemical composition, and mineral structure. Iodide uptake experiments were completed with each of these minerals in a range of swamping electrolyte identities (NaCl, NaBr, KCl) and concentrations. Iodide uptake behaviors form distinct trends with cation exchange capacity and mineral structure. These trends change substantially with electrolyte composition and concentration, but do not appear to be affected by solution pH. The experimental results suggest that iodide may directly interact with clays by forming ion-pairs (e.g., NaI(aq)) which may concentrate within the interlayer space as well as the thin areas surrounding the clay particle where water behavior is more structured relative to bulk water. Ion pairing and iodide concentration in these zones is probably driven by the reduced dielectric constant of water in confined space and by the relatively high polarizability of the iodide species. PMID:26057987

  5. Ionic conductivity and thermoelectric power of pure and Al2O3-dispersed AgI

    NASA Technical Reports Server (NTRS)

    Shahi, K.; Wagner, J. B., Jr.

    1981-01-01

    Ionic and electronic conductivities, and thermoelectric power have been measured for AgI and AgI containing a dispersion of submicron size Al2O3 particles. While the dispersion of Al2O3 enhances the ionic conductivity significantly, it does not affect the electronic properties of the matrix. The enhancement is a strong function of the size and concentration of the dispersoid. Various models have been tested to account for the enhanced conduction. However, the complex behavior of the present results points out the need for more sophisticated theoretical models. Ionic conduction and thermoelectric power data suggest that the dispersed Al2O3 generates an excess of cation vacancies and thereby enhances the conductivity and suppresses the thermoelectric power of the matrix. The individual heats of transport of cation interstitials and vacancies have been estimated and compared to their respective migration energies.

  6. Focal Plane Detectors for the Advanced Gamma-Ray Imaging System (AGIS)

    SciTech Connect

    Otte, A. N.; Williams, D. A.; Byrum, K.; Drake, G.; Horan, D.; Smith, A.; Wagner, R. G.; Falcone, A.; Funk, S.; Tajima, H.; Mukherjee, R.

    2008-12-24

    The Advanced Gamma-Ray Imaging System (AGIS) is a concept for the next generation observatory in ground-based very high energy gamma-ray astronomy. Design goals are ten times better sensitivity, higher angular resolution, and a lower energy threshold than existing Cherenkov telescopes. Simulations show that a substantial improvement in angular resolution may be achieved if the pixel diameter is reduced to the order of 0.05 deg, i.e. two to three times smaller than the pixel diameter of current Cherenkov telescope cameras. At these dimensions, photon detectors with smaller physical dimensions can be attractive alternatives to the classical photomultiplier tube (PMT). Furthermore, the operation of an experiment with the size of AGIS requires photon detectors that are among other things more reliable, more durable, and possibly higher efficiency photon detectors. Alternative photon detectors we are considering for AGIS include both silicon photomultipliers (SiPMs) and multi-anode photomultipliers (MAPMTs). Here we present results from laboratory testing of MAPMTs and SiPMs along with results from the first incorporation of these devices into cameras on test bed Cherenkov telescopes.

  7. Influence of chloride and metals on silver bioavailability to Atlantic salmon (Salmo salar) and Rainbow trout (Oncorhynchus mykiss) yolk-sac fry.

    PubMed

    Bury, Nicolas R; Hogstrand, Christer

    2002-07-01

    The effects of differing water chloride concentrations (0-10 mM) or competing metals [Cu(II), Cd(II), Zn(II), Pb(II), Co(II) (1-10,000 nM)] on Ag(I) uptake in yolk-sac fry of two salmonid species, the Atlantic salmon (Salmo salar) and rainbow trout (Oncorhynchus mykiss), were studied. None of the metals tested were strong competitors of Atlantic salmon yolk-sac fry whole body Ag(I) influx. Inhibition of Ag(I) influx was only seen with a 100-fold excess of Cu(II) or Cd(II) or a 1000-fold excess of Pb(II) or Co(II). At these concentrations, the degree of competition appears to be directly proportional to the conditional stability constant of the competing metal to the gill (metal-gill log K). The range of [Cl-] allowed an assessment of Ag+, AgCl(aq), and AgCl2- bioavailability. The pattern of Ag(I) uptake was similar for each fish species. At <1 mM Cl-, where the [Ag+] dominates, the Ag(I) accumulation rate was constant. Above 1 mM Cl-, where the [AgCl(aq)] is dominant and the [AgCl2-] increases, there was a decline in Ag(I) uptake rate. However, even when very little Ag+ was present (i.e., at 10 mM Cl-) Ag(I) accumulated, albeit at a lower rate. This was suggestive of passive influx by AgCl(aq) and indicated little or no entry of negatively charged silver chloride complexes. The decline in Ag(I) uptake above 1 mM Cl- demonstrated that, if Ag(I) was present as both Ag+ and AgCl(aq), salmonid Ag(I) accumulation was dominated by Ag+ uptake. Therefore, the order of bioavailability of the Ag(I) species was determined as Ag+ > AgCl(aq) > AgCl2-. PMID:12144263

  8. Characterization and antibacterial activity of silver exchanged regenerated NaY zeolite from surfactant-modified NaY zeolite.

    PubMed

    Salim, Mashitah Mad; Malek, Nik Ahmad Nizam Nik

    2016-02-01

    The antibacterial activity of regenerated NaY zeolite (thermal treatment from cetyltrimethyl ammonium bromide (CTAB)-modified NaY zeolite and pretreatment with Na ions) loaded with silver ions were examined using the broth dilution minimum inhibitory concentration (MIC) method against Escherichia coli (E. coli ATCC 11229) and Staphylococcus aureus (S. aureus ATCC 6538). X-ray diffraction (XRD), attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy, field emission scanning electron microscopy (FESEM), energy dispersive X-ray (EDX) and chemical elemental analyses were used to characterize the regenerated NaY and AgY zeolites. The XRD patterns indicated that the calcination and addition of silver ions on regenerated NaY zeolite did not affect the structure of the regenerated NaY zeolite as the characteristic peaks of the NaY zeolite were retained, and no new peaks were observed. The regenerated AgY zeolite showed good antibacterial activity against both bacteria strains in distilled water, and the antibacterial activity of the samples increased with increasing Ag loaded on the regenerated AgY zeolite; the regenerated AgY zeolite was more effective against E. coli than S. aureus. However, the antibacterial activity of the regenerated AgY was not effective in saline solution for both bacteria. The study showed that CTAB-modified NaY zeolite materials could be regenerated to NaY zeolite using thermal treatment (550°C, 5h) and this material has excellent performance as an antibacterial agent after silver ions loading. PMID:26652350

  9. Neutron Detection with Mercuric Iodide

    SciTech Connect

    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.

  10. Reclaiming silver from silver zeolite

    SciTech Connect

    Reimann, G.A.

    1991-10-01

    Silver zeolite is used to capture radioiodines from air cleaning systems in some nuclear facilities at the Idaho National Engineering Laboratory. It may become radioactively contaminated and/or poisoned by hydrocarbon vapors, which diminishes its capacity for iodine. Silver zeolite contains up to 38 wt% silver. A pyrometallurgical process was developed to reclaim the silver before disposing of the unserviceable zeolite as a radioactive waste. A flux was formulated to convert the refractory aluminosilicate zeolite structure into a low-melting fluid slag, with Na[sub 2]O added as NAOH instead of Na[sub 2]CO[sub 3] to avoid severe foaming due to CO[sub 2] evolution. A propane-fired furnace was built to smelt 45 kg charges at 1300C in a carbon-bonded silicon carbide crucible. A total of 218 kg (7000 tr oz) of silver was reclaimed from 1050 kg of unserviceable zeolite. Silver recoveries of 97% were achieved, and the radioisotopes were fixed as stable silicates in a vitreous slag that was disposed of as a low level waste. Recovered silver was refined using oxygen and cast into 100 tr oz bars assaying 99.8+% silver and showing no radioactive contamination.

  11. Reclaiming silver from silver zeolite

    SciTech Connect

    Reimann, G.A.

    1991-10-01

    Silver zeolite is used to capture radioiodines from air cleaning systems in some nuclear facilities at the Idaho National Engineering Laboratory. It may become radioactively contaminated and/or poisoned by hydrocarbon vapors, which diminishes its capacity for iodine. Silver zeolite contains up to 38 wt% silver. A pyrometallurgical process was developed to reclaim the silver before disposing of the unserviceable zeolite as a radioactive waste. A flux was formulated to convert the refractory aluminosilicate zeolite structure into a low-melting fluid slag, with Na{sub 2}O added as NAOH instead of Na{sub 2}CO{sub 3} to avoid severe foaming due to CO{sub 2} evolution. A propane-fired furnace was built to smelt 45 kg charges at 1300C in a carbon-bonded silicon carbide crucible. A total of 218 kg (7000 tr oz) of silver was reclaimed from 1050 kg of unserviceable zeolite. Silver recoveries of 97% were achieved, and the radioisotopes were fixed as stable silicates in a vitreous slag that was disposed of as a low level waste. Recovered silver was refined using oxygen and cast into 100 tr oz bars assaying 99.8+% silver and showing no radioactive contamination.

  12. Predissociation dynamics of lithium iodide

    SciTech Connect

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

    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.

  13. Expanded Analysis of Hot Isostatic Pressed Iodine-Loaded Silver-Exchanged Mordenite

    SciTech Connect

    Jubin, R. T.; Bruffey, S. H.; Patton, K. K.

    2014-09-30

    Reduced silver-exchanged mordenite (Ag0Z) is being evaluated as a potential material to control the release of radioactive iodine that is released during the reprocessing of used nuclear fuel into the plant off-gas streams. The purpose of this study was to determine if hot pressing could directly convert this iodine loaded sorbent into a waste form suitable for long-term disposition. The minimal pretreatment required for production of pressed pellets makes hot pressing a technically and economically desirable process. Initial scoping studies utilized hot uniaxial pressing (HUPing) to prepare samples of non-iodine-loaded reduced silver exchanged mordenite (Ag0Z). The resulting samples were very fragile due to the low pressure (~ 28 MPa) used. It was recommended that hot isostatic pressing (HIPing), performed at higher temperatures and pressures, be investigated. HIPing was carried out in two phases, with a third and final phase currently underway. Phase I evaluated the effects of pressure and temperature conditions on the manufacture of a pressed sample. The base material was an engineered form of silver zeolite. Six samples of Ag0Z and two samples of I-Ag0Z were pressed. It was found that HIPing produced a pressed pellet of high density. Analysis of each pressed pellet by scanning electron microscopy-energy dispersive spectrophotometry (SEM-EDS) and X-ray diffraction (XRD) demonstrated that under the conditions used for pressing, the majority of the material transforms into an amorphous structure. The only crystalline phase observed in the pressed Ag0Z material was SiO2. For the samples loaded with iodine (I-Ag0Z) iodine was present as AgI clusters at low temperatures, and transformed into AgIO4 at high temperatures. Surface mapping and EDS demonstrate segregation between silver iodide phases and silicon dioxide phases. Based on the results of the Phase I study, an expanded test matrix was developed to examine the effects of multiple source materials, compositional

  14. Colorimetric Solid Phase Extraction for the Measurement of Total I (Iodine, Iodide, and Triiodide) in Spacecraft Drinking Water

    NASA Technical Reports Server (NTRS)

    Lipert, Robert J.; Porter, Marc D.; Siperko, Lorraine M.; Gazda, Daniel B.; Rutz, Jeff A.; Schultz, John R.; Carrizales, Stephanie M.; McCoy, J. Torin

    2009-01-01

    An experimental drinking water monitoring kit for the measurement of iodine and silver(I) was recently delivered to the International Space Station (ISS). The kit is based on Colorimetric Solid Phase Extraction (CSPE) technology, which measures the change in diffuse reflectance of indicator disks following exposure to a water sample. To satisfy additional spacecraft water monitoring requirements, CSPE has now been extended to encompass the measurement of total I (iodine, iodide, and triiodide) through the introduction of an oxidizing agent, which converts iodide and triiodide to iodine, for measurement using the same indicator disks currently being tested on ISS. These disks detect iodine, but are insensitive to iodide and triiodide. We report here the operational considerations, design, and ground-based performance of the CSPE method for total I. The results demonstrate that CSPE technology is poised to meet NASA's total I monitoring requirements.

  15. Mercuric iodide light detector and related method

    DOEpatents

    Iwanczyk, Jan S.; Barton, Jeff B.; Dabrowski, Andrzej J.; Schnepple, Wayne F.

    1986-01-01

    Apparatus and method for detecting light involve applying a substantially uniform electrical potential difference between first and second spaced surfaces of a body of mercuric iodide, exposing the first surface to light and measuring an electrical current passed through the body in response to the light. The mercuric iodide may be substantially monocrystalline and the potential may be applied between a substantially transparent conductive layer at the first surface and a second conductive layer at the second surface. In a preferred embodiment, the detector is coupled to a scintillator for passage of light to the mercuric iodide in response to ionizing radiation incident on the scintillator.

  16. Mercuric iodide light detector and related method

    DOEpatents

    Iwanczyk, J.S.; Barton, J.B.; Dabrowski, A.J.; Schnepple, W.F.

    1986-09-23

    Apparatus and method for detecting light involve applying a substantially uniform electrical potential difference between first and second spaced surfaces of a body of mercuric iodide, exposing the first surface to light and measuring an electrical current passed through the body in response to the light. The mercuric iodide may be substantially monocrystalline and the potential may be applied between a substantially transparent conductive layer at the first surface and a second conductive layer at the second surface. In a preferred embodiment, the detector is coupled to a scintillator for passage of light to the mercuric iodide in response to ionizing radiation incident on the scintillator. 7 figs.

  17. Lithium iodide cardiac pacemakers: initial clinical experience.

    PubMed Central

    Burr, L. H.

    1976-01-01

    A new long-life cardiac pacemaker pulse generator powered by a lithium iodide fuel cell was introduced in Canada in 1973. The compact, hermetically sealed unit is easily implanted and reliable, has excellent patient acceptance and has an anticipated battery life of almost 14 years. Among 105 patients who received a lithium iodide pacemaker, complications occurred in 18. The lithium iodide pacemaker represents a significant advance in pacemaker generator technology and is recommended for long-term cardiac pacing; the manufacturer guarantees the pulse generator for 6 years. Images FIG. 1 PMID:974965

  18. Iodide Protects Heart Tissue from Reperfusion Injury

    PubMed Central

    Iwata, Akiko; Morrison, Michael L.; Roth, Mark B.

    2014-01-01

    Iodine is an elemental nutrient that is essential for mammals. Here we provide evidence for an acute therapeutic role for iodine in ischemia reperfusion injury. Infusion of the reduced form, iodide, but not the oxidized form iodate, reduces heart damage by as much as 75% when delivered intravenously following temporary loss of blood flow but prior to reperfusion of the heart in a mouse model of acute myocardial infarction. Normal thyroid function may be required because loss of thyroid activity abrogates the iodide benefit. Given the high degree of protection and the high degree of safety, iodide should be explored further as a therapy for reperfusion injury. PMID:25379708

  19. 21 CFR 520.763b - Dithiazanine iodide powder.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Dithiazanine iodide powder. 520.763b Section 520... iodide powder. (a) Chemical name. 3-Ethyl-2- -benzothiazoliumiodide. (b) Specifications. Dithiazanine iodide powder contains 200 milligrams of dithiazanine iodide per level standard tablespoon. (c)...

  20. 21 CFR 520.763b - Dithiazanine iodide powder.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Dithiazanine iodide powder. 520.763b Section 520... iodide powder. (a) Chemical name. 3-Ethyl-2- -benzothiazoliumiodide. (b) Specifications. Dithiazanine iodide powder contains 200 milligrams of dithiazanine iodide per level standard tablespoon. (c)...

  1. AgI microplate monocrystals with polar {0001} facets: spontaneous photocarrier separation and enhanced photocatalytic activity.

    PubMed

    Kuang, Qin; Zheng, Xiaoli; Yang, Shihe

    2014-02-24

    Elucidating the facet-dependent photocatalytic activity of semiconductor photocatalysts is important in improving the overall efficiency of photocatalysis. Furthermore, combining facet control with selective deposition of oxidation and/or reduction cocatalysts on specific faces of semiconductor photocatalysts is potentially an effective strategy to synergistically optimize the functionality of photocatalysts. In the present study, high-purity wurtzite-type β-AgI platelet microcrystals with polar {0001} facets were prepared by a facile polyvinylpyrrolidone-assisted precipitation reaction. The polar-faceted AgI microplates were used as archetypes to demonstrate preferential diametric migration (i.e., effective separation) of photogenerated electrons and holes along the c axis. Such vectorial electron-hole separation stems from the asymmetric surface structures, which give rise to distinct photoexcited reaction behaviors on the ±(0001) polar facets of wurtzite-type semiconductors. Furthermore, on selective deposition of Ag and MnOx (1.5AgI microplates in degrading organic pollutants was dramatically enhanced thanks to the broad light-absorption range, strong dye-adsorption ability, and effective spatial separation of photocarriers. PMID:24449437

  2. Estimating the number of cases of acute gastrointestinal illness (AGI) associated with Canadian municipal drinking water systems.

    PubMed

    Murphy, H M; Thomas, M K; Medeiros, D T; McFADYEN, S; Pintar, K D M

    2016-05-01

    The estimated burden of endemic acute gastrointestinal illness (AGI) annually in Canada is 20·5 million cases. Approximately 4 million of these cases are domestically acquired and foodborne, yet the proportion of waterborne cases is unknown. A number of randomized controlled trials have been completed to estimate the influence of tap water from municipal drinking water plants on the burden of AGI. In Canada, 83% of the population (28 521 761 people) consumes tap water from municipal drinking water plants serving >1000 people. The drinking water-related AGI burden associated with the consumption of water from these systems in Canada is unknown. The objective of this research was to estimate the number of AGI cases attributable to consumption of drinking water from large municipal water supplies in Canada, using data from four household drinking water intervention trials. Canadian municipal water treatment systems were ranked into four categories based on source water type and quality, population size served, and treatment capability and barriers. The water treatment plants studied in the four household drinking water intervention trials were also ranked according to the aforementioned criteria, and the Canadian treatment plants were then scored against these criteria to develop four AGI risk groups. The proportion of illnesses attributed to distribution system events vs. source water quality/treatment failures was also estimated, to inform the focus of future intervention efforts. It is estimated that 334 966 cases (90% probability interval 183 006-501 026) of AGI per year are associated with the consumption of tap water from municipal systems that serve >1000 people in Canada. This study provides a framework for estimating the burden of waterborne illness at a national level and identifying existing knowledge gaps for future research and surveillance efforts, in Canada and abroad. PMID:26564554

  3. Unusual N-H activation of 2-aminopyrimidine: supramolecular assembly into an Ag(I) metal-organic framework.

    PubMed

    Liu, Fu-Ling; Xu, Zheng-Hu; Zhang, Xi-Ying; Wang, Xing-Po; Sun, Di

    2014-02-01

    A rare example of coordination at the amino group of NH2 pym (2-aminopyrimidine) relevant to N-H activation is described that leads to a novel Ag(I) -imide 3D metal-organic framework (MOF). The coordination of Ag(I) to NH2 pym produced an electron-withdrawing effect and thus increased its acidity, which facilitated the N-H activation and the subsequent formation of the Ag-imide bond. A cooperative metalation/deprotonation process for the N-H activation of NH2 pym is suggested. Interestingly, photoluminescence of 1 is switched on at the low temperature of 77 K. PMID:24227790

  4. Reversible photoswitching behavior in bulk resistance and in color of polycrystalline AgI at room temperature

    SciTech Connect

    Khaton, Rahima; Kashiwagi, Shin-ichiro; Iimori, Toshifumi; Ohta, Nobuhiro

    2008-12-08

    A photoinduced reversible change in bulk resistance of polycrystalline AgI is observed at room temperature. The original yellow color of the sample changes to dark brown with UV (308 nm) photoirradiation, associated with the small decrease in the bulk resistance. A reversible switching of color between dark brown and yellow is observed by alternative UV-visible photoirradiation, associated with a switching between high and low resistance states. The observed reversible photoswitching is interpreted in terms of the photoinduced reversible change in the {beta}-{gamma}-polytype stacking structure of the polycrystalline AgI.

  5. Iodide transport: implications for health and disease.

    PubMed

    Pesce, Liuska; Kopp, Peter

    2014-01-01

    Disorders of the thyroid gland are among the most common conditions diagnosed and managed by pediatric endocrinologists. Thyroid hormone synthesis depends on normal iodide transport and knowledge of its regulation is fundamental to understand the etiology and management of congenital and acquired thyroid conditions such as hypothyroidism and hyperthyroidism. The ability of the thyroid to concentrate iodine is also widely used as a tool for the diagnosis of thyroid diseases and in the management and follow up of the most common type of endocrine cancers: papillary and follicular thyroid cancer. More recently, the regulation of iodide transport has also been the center of attention to improve the management of poorly differentiated thyroid cancer. Iodine deficiency disorders (goiter, impaired mental development) due to insufficient nutritional intake remain a universal public health problem. Thyroid function can also be influenced by medications that contain iodide or interfere with iodide metabolism such as iodinated contrast agents, povidone, lithium and amiodarone. In addition, some environmental pollutants such as perchlorate, thiocyanate and nitrates may affect iodide transport. Furthermore, nuclear accidents increase the risk of developing thyroid cancer and the therapy used to prevent exposure to these isotopes relies on the ability of the thyroid to concentrate iodine. The array of disorders involving iodide transport affect individuals during the whole life span and, if undiagnosed or improperly managed, they can have a profound impact on growth, metabolism, cognitive development and quality of life. PMID:25009573

  6. A perchlorate sensitive iodide transporter in frogs

    PubMed Central

    Carr, Deborah L.; Carr, James A.; Willis, Ray E.; Pressley, Thomas A.

    2008-01-01

    Nucleotide sequence comparisons have identified a gene product in the genome database of African clawed frogs (Xenopus laevis) as a probable member of the solute carrier family of membrane transporters. To confirm its identity as a putative iodide transporter, we examined the function of this sequence after heterologous expression in mammalian cells. A green monkey kidney cell line transfected with the Xenopus nucleotide sequence had significantly greater 125I uptake than sham-transfected control cells. The uptake in carrier-transfected cells was significantly inhibited in the presence of perchlorate, a competitive inhibitor of mammalian Na+/iodide symporter. Tissue distributions of the sequence were also consistent with a role in iodide uptake. The mRNA encoding the carrier was found to be expressed in the thyroid gland, stomach, and kidney of tadpoles from X. laevis, as well as the bullfrog Rana catesbeiana. The ovaries of adult X. laevis also were found to express the carrier. Phylogenetic analysis suggested that the putative X. laevis iodide transporter is orthologous to vertebrate Na+-dependent iodide symporters. We conclude that the amphibian sequence encodes a protein that is indeed a functional Na+/iodide symporter in Xenopus laevis, as well as Rana catesbeiana. PMID:18275962

  7. Recovery of anhydrous hydrogen iodide

    DOEpatents

    O'Keefe, Dennis R.; McCorkle, Jr., Kenneth H.; de Graaf, Johannes D.

    1982-01-01

    Relatively dry hydrogen iodide can be recovered from a mixture of HI, I.sub.2 and H.sub.2 O. After the composition of the mixture is adjusted so that the amounts of H.sub.2 O and I.sub.2 do not exceed certain maximum limits, subjection of the mixture to superatmospheric pressure in an amount equal to about the vapor pressure of HI at the temperature in question causes distinct liquid phases to appear. One of the liquid phases contains HI and not more than about 1 weight percent water. Often the adjustment in the composition will include the step of vaporization, and the distinct layers appear following the increase in pressure of the vapor mixture. Adjustment in the composition may also include the addition of an extraction agent, such as H.sub.3 PO.sub.4, and even though the adjusted composition mixture contains a significant amount of such an agent, the creation of the distinct liquid phases is not adversely affected.

  8. Formation of methyl iodide on a natural manganese oxide.

    PubMed

    Allard, Sébastien; Gallard, Hervé; Fontaine, Claude; Croué, Jean-Philippe

    2010-08-01

    This paper demonstrates that manganese oxides can initiate the formation of methyl iodide, a volatile compound that participates to the input of iodine into the atmosphere. The formation of methyl iodide was investigated using a natural manganese oxide in batch experiments for different conditions and concentrations of iodide, natural organic matter (NOM) and manganese oxide. Methyl iodide was formed at concentrations iodide concentrations ranging from 0.8 to 38.0 mg L(-1). The production of methyl iodide increased with increasing initial concentrations of iodide ion and Mn sand and when pH decreased from 7 to 5. The hydrophilic NOM isolate exhibited the lowest yield of methyl iodide whereas hydrophobic NOM isolates such as Suwannee River HPOA fraction produced the highest concentration of methyl iodide. The formation of methyl iodide could take place through the oxidation of NOM on manganese dioxide in the presence of iodide. However, the implication of elemental iodine cannot be excluded at acidic pH. Manganese oxides can then participate with ferric oxides to the formation of methyl iodide in soils and sediments. The formation of methyl iodide is unlikely in technical systems such as drinking water treatment i.e. for ppt levels of iodide and low contact times with manganese oxides. PMID:20580399

  9. A Porphyrin Coordination Cage Assembled from Four Silver(I) Triazolyl-Pyridine Complexes.

    PubMed

    Ballester, Pablo; Claudel, Mickaël; Durot, Stéphanie; Kocher, Lucas; Schoepff, Laetitia; Heitz, Valérie

    2015-10-19

    The synthesis of a zinc(II) porphyrin 1 with four appended triazolyl-pyridine chelates is reported. Complexation of the porphyrin peripheral ligands with Ag(I) ions in a 1:2 binding stoichiometry afforded quantitatively the coordination cage [Ag4 (1)2 ](4+) . The assembly and disassembly processes of the cage were investigated in solution using UV/Vis spectroscopy. The mathematical analysis of the data obtained in the UV/Vis titration of 1 with Ag(I) confirmed the assembly in CH2 Cl2 /MeOH (90:10) solution of a species having a 1:2 porphyrin/silver stoichiometry and assigned to it an overall stability constant of 5.0×10(26)  M(-5) . The use of a model system allowed an independent assessment of a microscopic binding constant value (Km ) for the interaction between the triazolyl-pyridine ligand and Ag(I) . The coincidence that existed between the Km values extracted from the model system and the titration of 1 provided an indication of the quality and fit of the data analysis. It also allowed the calculation of the average effective molarity (EM) value for the three intramolecular processes that led to the cage assembly as 2.6 mM. Simulated speciation profiles supported the conclusion that at millimolar concentration and working under strict stoichiometric control of the silver/porphyrin ratio, the cage [Ag4 (1)2 ](4+) was the species exclusively assembled in solution. On the other hand, when the concentration of added Ag(I) was approximately 2.6 mM, 50 % of the coordination cage disassembled into open aggregates. PMID:26338089

  10. A Topological Array Trigger for AGIS, the Advanced Gamma ray Imaging System

    SciTech Connect

    Krennrich, F.; Anderson, J.; Byrum, K.; Dawson, J.; Drake, G.; Haberichter, W.; Kreps, A.; Smith, A.; Buckley, J.; Krawczynski, H.; Imran, A.; Schroedter, M.

    2008-12-24

    Next generation ground based {gamma}-ray observatories such as AGIS{sup 1} and CTA{sup 2} are expected to cover a 1 km{sup 2} area with 50-100 imaging atmospheric Cherenkov telescopes. The stereoscopic view ol air showers using multiple view points raises the possibility to use a topological array trigger that adds substantial flexibility, new background suppression capabilities and a reduced energy threshold. In this paper we report on the concept and technical implementation of a fast topological trigger system, that makes use of real time image processing of individual camera patterns and their combination in a stereoscopic array analysis. A prototype system is currently under construction and we discuss the design and hardware of this topological array trigger system.

  11. Iodide sorption to subsurface sediments and illitic minerals

    SciTech Connect

    Kaplan, Daniel I.; Serne, R. Jeffrey; Parker, Kent E.; Kutnyakov, Igor V.

    2000-02-01

    Laboratory studies were conducted to quantify and understand the processes by which iodide (I-) adsorbs to subsurface arid sediments. A surprisingly large amount of I- sorbed (distribution coefficients [Kd?s] ranged from 1 to 10 mL/g and averaged 3.3 mL/g) to three alkaline subsurface sediments that were low in organic matter content. Experiments with pure mineral isolates, similar to the minerals identified in the clay fraction of the sediments, showed that there was little or no I- sorption. The pure minerals that had low iodide sorption include montmorillonite (Kd = -0.42 +/- 0.08 mL/g), quartz (Kd = 0.04 +/- 0.02 mL/g), vermiculite (Kd = 0.56 +/- 0.21 mL/g), calcite (Kd = 0.04 +/- 0.01 mL/g), goethite (Kd = 0.10 +/- 0.03 mL/g), or chlorite (Kd = -0.22 +/- 0.06 mL/g). Conversely, a significant amount of I- sorbed to illite (Kd = 15.14 +/- 2.84 mL/g). Upon treating the iodide-laden illite with dissolved F-, Cl-, Br-, or I-127, desorption (or isotopic exchange in the case of I-127) removed, respectively, 57 +/- 3%, 55 +/- 0%, 48 +/- 3, and 17 +/- 1% of the I- originally adsorbed to the illite. The fact that such large amounts of I- could be desorbed suggests that the I- was weakly adsorbed, and not chemically bonded to a soft metal, such as mercury or silver, that may have existed in the illite structure as trace impurities. Finally, I- sorption to illite was strongly pH-dependent; the Kd values decreased from 46 to 22 mL/g as the pH increased from 3.6 to 9.4. Importantly, I- sorbed to illite even under alkaline conditions. Together, these experiments suggest that illite removed I- from the aqueous phase predominantly by reversible physical adsorption to the pH-dependent edge sites. Illites may constitute a substantial proportion of the clay-size fraction of many arid sediments and therefore may play an important role in retarding I- movement in these sediments.

  12. Simplifying the growth of hybrid single-crystals by using nanoparticle precursors: the case of AgI

    NASA Astrophysics Data System (ADS)

    Xu, Biao; Wang, Ruji; Wang, Xun

    2012-03-01

    We report the synthesis of a series of AAgmIn single-crystals within 24 h, at room temperature, utilizing AgI nanoparticles (NPs) as the precursor. The AgI NPs impart high reactivity under mild conditions and favor the growth kinetics. 0D, 1D and 2D iodoargentate crystals can be obtained. This work represents the first application of NPs in the field of organo-metal-halide crystals and will inspire the design of other AMmXn crystals.We report the synthesis of a series of AAgmIn single-crystals within 24 h, at room temperature, utilizing AgI nanoparticles (NPs) as the precursor. The AgI NPs impart high reactivity under mild conditions and favor the growth kinetics. 0D, 1D and 2D iodoargentate crystals can be obtained. This work represents the first application of NPs in the field of organo-metal-halide crystals and will inspire the design of other AMmXn crystals. Electronic supplementary information (ESI) available: XPS spectra of AgI NPs, schematic representation of the formation process of [Ag4I8]4- in 2, UV-Vis spectra of the DTMA-Ag-I clusters, analysis of force balance of a crystal at the interface between H2O and CH2Cl2 and crystal structure depiction of 1-4. CIF files of 1-4 are also provided. CCDC reference numbers 863848, 863849, 863850 and 863851. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c2nr30139c

  13. Silver cyanide

    Integrated Risk Information System (IRIS)

    Silver cyanide ; CASRN 506 - 64 - 9 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic Ef

  14. Energy resolution enhancement of mercuric iodide detectors

    NASA Technical Reports Server (NTRS)

    Finger, M.; Prince, T. A.; Padgett, L.; Prickett, B.; Schnepple, W.

    1984-01-01

    A pulse processing technique has been developed which improves the gamma-ray energy resolution of mercuric iodide detectors. The technique employs a fast (100 ns) and a slow (6.4 microsec) pulse height analysis to correct for signal variations due to variations in charge trapping. The capabilities of the technique for energy resolution enhancement are discussed as well as the utility of the technique for examining the trapping characteristics of individual detectors. An energy resolution of 2.6 percent FWHM at 662 keV was achieved with an acceptance efficiency of 100 percent from a mercuric iodide detector which gives 8.3 percent FWHM using standard techniques.

  15. Simplest Formula of Copper Iodide: A Stoichiometry Experiment.

    ERIC Educational Resources Information Center

    MacDonald, D. J.

    1983-01-01

    Describes an experiment presented to students as a problem in determining the stoichiometry of "copper iodide" to decide whether it is cuprous iodide or cupric iodide. The experiment illustrates stoichiometry principles, providing experiences with laboratory techniques and numerical computation. Detailed outline (written for student use) is…

  16. Barium iodide and strontium iodide crystals andd scintillators implementing the same

    DOEpatents

    Payne, Stephen A; Cherepy, Nerine J; Hull, Giulia E; Drobshoff, Alexander D; Burger, Arnold

    2013-11-12

    In one embodiment, a material comprises a crystal comprising strontium iodide providing at least 50,000 photons per MeV. A scintillator radiation detector according to another embodiment includes a scintillator optic comprising europium-doped strontium iodide providing at least 50,000 photons per MeV. A scintillator radiation detector in yet another embodiment includes a scintillator optic comprising SrI.sub.2 and BaI.sub.2, wherein a ratio of SrI.sub.2 to BaI.sub.2 is in a range of between 0:1 A method for manufacturing a crystal suitable for use in a scintillator includes mixing strontium iodide-containing crystals with a source of Eu.sup.2+, heating the mixture above a melting point of the strontium iodide-containing crystals, and cooling the heated mixture near the seed crystal for growing a crystal. Additional materials, systems, and methods are presented.

  17. Determine Minimum Silver Flake Addition to GCM for Iodine Loaded AgZ

    SciTech Connect

    Garino, Terry J.; Nenoff, Tina M.; Rodriguez, Mark A.

    2014-04-01

    The minimum amount of silver flake required to prevent loss of I{sub 2} during sintering in air for a SNL Glass Composite Material (GCM) Waste Form containing AgI-MOR (ORNL, 8.7 wt%) was determined to be 1.1 wt% Ag. The final GCM composition prior to sintering was 20 wt% AgI-MOR, 1.1 wt% Ag, and 80 wt% Bi-Si oxide glass. The amount of silver flake needed to suppress iodine loss was determined using thermo gravimetric analysis with mass spectroscopic off-gas analysis. These studies found that the ratio of silver to AgI-MOR required is lower in the presence of the glass than without it. Therefore an additional benefit of the GCM is that it serves to inhibit some iodine loss during processing. Alternatively, heating the AgI-MOR in inert atmosphere instead of air allowed for densified GCM formation without I{sub 2} loss, and no necessity for the addition of Ag. The cause of this behavior is found to be related to the oxidation of the metallic Ag to Ag{sup +} when heated to above ~300{degrees}C in air. Heating rate, iodine loading levels and atmosphere are the important variables that determine AgI migration and results suggest that AgI may be completely incorporated into the mordenite structure by the 550{degrees}C sintering temperature.

  18. The Advanced Gamma-ray Imaging System (AGIS)--Science Highlights

    SciTech Connect

    Buckley, J.; Krawczynski, H.; Coppi, P.; Digel, S.; Funk, S.; Krennrich, F.; Pohl, M.; Romani, R.; Vassiliev, V.

    2008-12-24

    The Advanced Gamma-ray Imaging System (AGIS), a future gamma-ray telescope consisting of an array of {approx}50 atmospheric Cherenkov telescopes distributed over an area of {approx}1 km{sup 2}, will provide a powerful new tool for exploring the high-energy universe. The order-of-magnitude increase in sensitivity and improved angular resolution could provide the first detailed images of {gamma}-ray emission from other nearby galaxies or galaxy clusters. The large effective area will provide unprecedented sensitivity to short transients (such as flares from AGNs and GRBs) probing both intrinsic spectral variability (revealing the details of the acceleration mechanism and geometry) as well as constraining the high-energy dispersion in the velocity of light (probing the structure of spacetime and Lorentz invariance). A wide field of view ({approx}4 times that of current instruments) and excellent angular resolution (several times better than current instruments) will allow for an unprecedented survey of the Galactic plane, providing a deep unobscured survey of SNRs, X-ray binaries, pulsar-wind nebulae, molecular cloud complexes and other sources. The differential flux sensitivity of {approx}10{sup -13} erg cm{sup -2} sec{sup -1} will rival the most sensitive X-ray instruments for these extended Galactic sources. The excellent capabilities of AGIS at energies below 100 GeV will provide sensitivity to AGN and GRBs out to cosmological redshifts, increasing the number of AGNs detected at high energies from about 20 to more than 100, permitting population studies that will provide valuable insights into both a unified model for AGN and a detailed measurement of the effects of intergalactic absorption from the diffuse extragalactic background light. A new instrument with fast-slewing wide-field telescopes could provide detections of a number of long-duration GRBs providing important physical constraints from this new spectral component. The new array will also have excellent

  19. 21 CFR 184.1265 - Cuprous iodide.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Cuprous iodide. 184.1265 Section 184.1265 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) DIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE Listing of Specific Substances Affirmed as GRAS §...

  20. 21 CFR 184.1265 - Cuprous iodide.

    Code of Federal Regulations, 2010 CFR

    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...

  1. Developments in mercuric iodide gamma ray imaging

    NASA Astrophysics Data System (ADS)

    Patt, B. E.; Beyerle, A. G.; Dolin, R. C.; Ortale, C.

    A mercuric iodide gamma-ray imaging array and camera system previously described has been characterized for spatial and energy resolution. Based on this data a new camera is being developed to more fully exploit the potential of the array. Characterization results and design criterion for the new camera will be presented.

  2. Developments in mercuric iodide gamma ray imaging

    NASA Astrophysics Data System (ADS)

    Patt, B. E.; Beyerle, A. G.; Dolin, R. C.; Ortale, C.

    1989-11-01

    A mercuric iodide (HgI2) gamma ray imaging array and camera system previously described have been characterized for spatial and energy resolution. Based on these data a new camera is being developed to more fully exploit the potential of the array. Characterization results and design criteria for the new camera will be presented.

  3. Methyl Iodide Fumigation of Bacillus anthracis Spores.

    PubMed

    Sutton, Mark; Kane, Staci R; Wollard, Jessica R

    2015-09-01

    Fumigation techniques such as chlorine dioxide, vaporous hydrogen peroxide, and paraformaldehyde previously used to decontaminate items, rooms, and buildings following contamination with Bacillus anthracis spores are often incompatible with materials (e.g., porous surfaces, organics, and metals), causing damage or residue. Alternative fumigation with methyl bromide is subject to U.S. and international restrictions due to its ozone-depleting properties. Methyl iodide, however, does not pose a risk to the ozone layer and has previously been demonstrated as a fumigant for fungi, insects, and nematodes. Until now, methyl iodide has not been evaluated against Bacillus anthracis. Sterne strain Bacillus anthracis spores were subjected to methyl iodide fumigation at room temperature and at 550C. Efficacy was measured on a log-scale with a 6-log reduction in CFUs being considered successful compared to the U.S. Environmental Protection Agency biocide standard. Such efficacies were obtained after just one hour at 55 °C and after 12 hours at room temperature. No detrimental effects were observed on glassware, PTFE O-rings, or stainless steel. This is the first reported efficacy of methyl iodide in the reduction of Bacillus anthracis spore contamination at ambient and elevated temperatures. PMID:26502561

  4. Scintillator handbook with emphasis on cesium iodide

    NASA Technical Reports Server (NTRS)

    Tidd, J. L.; Dabbs, J. R.; Levine, N.

    1973-01-01

    This report provides a background of reasonable depth and reference material on scintillators in general. Particular attention is paid to the cesium iodide scintillators as used in the High Energy Astronomy Observatory (HEAO) experiments. It is intended especially for use by persons such as laboratory test personnel who need to obtain a working knowledge of these materials and their characteristics in a short time.

  5. Iodide effects in transition metal catalyzed reactions.

    PubMed

    Maitlis, Peter M; Haynes, Anthony; James, Brian R; Catellani, Marta; Chiusoli, Gian Paolo

    2004-11-01

    The unique properties of I(-) allow it to be involved in several different ways in reactions catalyzed by the late transition metals: in the oxidative addition, the migration, and the coupling/reductive elimination steps, as well as in substrate activation. Most steps are accelerated by I(-)(for example through an increased nucleophilicity of the metal center), but some are retarded, because a coordination site is blocked. The "soft" iodide ligand binds more strongly to soft metals (low oxidation state, electron rich, and polarizable) such as the later and heavier transition metals, than do the other halides, or N- and O-centered ligands. Hence in a catalytic cycle that includes the metal in a formally low oxidation state there will be less tendency for the metal to precipitate (and be removed from the cycle) in the presence of I(-) than most other ligands. Iodide is a good nucleophile and is also easily and reversibly oxidized to I(2). In addition, I(-) can play key roles in purely organic reactions that occur as part of a catalytic cycle. Thus to understand the function of iodide requires careful analysis, since two or sometimes more effects occur in different steps of one single cycle. Each of these topics is illustrated with examples of the influence of iodide from homogeneous catalytic reactions in the literature: methanol carbonylation to acetic acid and related reactions; CO hydrogenation; imine hydrogenation; and C-C and C-N coupling reactions. General features are summarised in the Conclusions. PMID:15510253

  6. Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene.

    PubMed

    Cardaioli, Elena; Malfatti, Edoardo; Da Pozzo, Paola; Gallus, Gian Nicola; Carluccio, Maria Alessandra; Rufa, Alessandra; Volpi, Nila; Dotti, Maria Teresa; Federico, Antonio

    2011-04-15

    We sequenced the mitochondrial genome from a patient with progressive mitochondrial myopathy associated with deafness, sporadic seizures, and histological and biochemical features of mitochondrial respiratory chain dysfunction. Direct sequencing showed a heteroplasmic mutation at nucleotide 12262 in the tRNASer(AGY) gene. RFLP analysis confirmed that 63% of muscle mtDNA harboured the mutation, while it was absent in all the other tissues. The mutation is predicted to influence the functional behaviour of the aminoacyl acceptor stem of the tRNA. Several point mutations on mitochondrial tRNA genes have been reported in patients affected by encephalomyopathies, but between them only four were reported for tRNASer(AGY). PMID:21257182

  7. Novel magnetite nanoparticle based on BODIPY as fluorescent hybrid material for Ag(I) detection in aqueous medium.

    PubMed

    Kursunlu, Ahmed Nuri; Ozmen, Mustafa; Guler, Ersin

    2016-06-01

    This manuscript describes a highly selective and ultra-sensitive detection of Ag(I) in aqueous solution using amine coated magnetite nanoparticles modified boron-dipyrromethene by spectrofluorometer. Fe3O4 nanoparticles were synthesized by co-precipitation of Fe(2+)and Fe(3+)in an ammonia solution. Amine modified Fe3O4 was prepared by using (3-aminopropyl)triethoxysilane as silanization agent. The covalent binding of boron-dipyrromethene to amine modified Fe3O4 was confirmed by means of Fourier Transform infrared spectroscopy, transmission electron microscopy, dynamic light scattering, UV-vis and fluorimeter measurements and obtained nanoparticle-boron dipyrromethene structure. The binding abilities of nanoparticle-boron dipyrromethene towards different metal ions have been investigated by some spectroscopic methods as UV-vis, fluorescence spectroscopy, Job plot, etc. and the novel surface displayed high selectivity and sensitivity for Ag(I) among all tested metals. PMID:27130108

  8. catena-Poly[[[(iminodiacetato-kappaO)silver(I)]-mu3-2-aminopyrimidine-kappa3N1:N2:N3] monohydrate]: a one-dimensional silver(I) coordination polymer with mixed ligands.

    PubMed

    Sun, Di; Luo, Geng-Geng; Huang, Rong-Bin; Zhang, Na; Zheng, Lan-Sun

    2009-08-01

    The title compound, {[Ag(C4H6NO4)(C4H5N3)].H2O}n, was synthesized by the reaction of silver(I) nitrate with 2-aminopyrimidine and iminodiacetic acid. X-ray analysis reveals that the crystal structure contains a one-dimensional ladder-like Ag(I) coordination polymer and that N-H...O and O-H...O hydrogen bonding results in a three-dimensional network. The Ag(I) centre is four-coordinated by three N atoms from three different 2-aminopyrimidine ligands and one O atom from one iminodiacetate ligand. Comparison of the structural features with previous findings suggests that the existence of a second ligand plays an important role in the construction of such polymer frameworks. PMID:19652307

  9. Ag(I) Ion Functionalized Porous Organic Polymers As a New Platform for Highly Selective Adsorption of Ethylene over Ethane

    SciTech Connect

    LI, Baiyan; Zhang, Yiming; Ma, Dingxuan; Wu, Zili; Ma, Shengqian

    2014-01-01

    We report herein a strategy of incorporating air stable Ag(I) ions into water stable, high surface area porous organic polymer (POP) affording significant increase in ethylene uptake capacity and extremely high Qst for ethylene (over 100 kJ/mol at low ethylene load-ing) as illustrated in the context of Ag(I) ion functionalized PAF-1, PAF-1-SO3Ag. IAST calculations using single-component-isotherm data and equimolar ethylene/ethane ratio at 296 K reveal PAF-1-SO3Ag shows exceptionally high ethylene/ethane adsorption selectivi-ty (Sads: 27 to 125), far surpassing benchmark zeolite and any other MOF reported in literature. This alongside excellent water/air stability, high ethylene uptake capacity, and mild regeneration requirements make PAF-1-SO3Ag hold promise for adsorption-based eth-ylene/ethane separations, paving a way to develop Ag(I) ion function-alized POPs as a new platform for highly selective adsorption of eth-ylene over ethane.

  10. Selective fluorogenic and chromogenic probe for detection of silver ions and silver nanoparticles in aqueous media.

    PubMed

    Chatterjee, Amrita; Santra, Mithun; Won, Nayoun; Kim, Sungjee; Kim, Jae Kyung; Kim, Seung Bin; Ahn, Kyo Han

    2009-02-18

    A novel rhodamine-based fluorogenic and chromogenic probe for Ag(+) ions in aqueous media is developed, which can be also used for the detection of AgNPs. The sensing mechanism is based on irreversible tandem ring-opening and -forming processes promoted by Ag(+)-coordination to the iodide of the probe, which is accompanied by both color and turn-on type fluorescence changes. The probe shows remarkably high selectivity over other metal ions and detects silver ions up to 14 ppb. PMID:19159289

  11. Detection and characterization of silver nanoparticles and dissolved species of silver in culture medium and cells by AsFlFFF-UV-Vis-ICPMS: application to nanotoxicity tests.

    PubMed

    Bolea, E; Jiménez-Lamana, J; Laborda, F; Abad-Álvaro, I; Bladé, C; Arola, L; Castillo, J R

    2014-03-01

    A methodology based on Asymmetric Flow Field-Flow Fractionation (AsFlFFF) coupled with UV-Vis absorption spectrometry and ICP mass spectrometry (ICPMS) has been developed and applied to the study of silver nanoparticles (AgNPs) and dissolved species of silver in culture media and cells used in cytotoxicity tests. The effect of a nano-silver based product (protein stabilized silver nanoparticles ca. 15 nm average diameter) on human hepatoma (HepG2) cell viability has been studied. UV-Vis absorption spectrometry provided information about the nature (organic vs. nanoparticle) of the eluted species, whereas the silver was monitored by ICPMS. A shift towards larger hydrodynamic diameters was observed in the AgNPs after a 24 hour incubation period in the culture medium, which suggests a "protein corona" effect. Silver(I) associated with proteins present in the culture medium has also been detected, as a consequence of the oxidation process experimented by the AgNPs. However, the Ag(I) released into the culture medium did not justify the toxicity levels observed. AgNPs associated with the cultured HepG2 cells were also identified by AsFlFFF, after applying a solubilisation process based on the use of tetramethylammonium hydroxide (TMAH) and Triton X-100. These results have been confirmed by transmission electronic microscopy (TEM) analysis of the fractions collected from the AsFlFFF. The effect of AgNPs on HepG2 cells has been compared to that caused by silver(I) as AgNO3 under the same conditions. The determination of the total content of silver in the cells confirms that a much larger mass of silver as AgNPs with respect to AgNO3 (16 to 1) is needed to observe a similar toxicity. PMID:24162133

  12. Influences of impurities on iodine removal efficiency of silver alumina adsorbent

    SciTech Connect

    Fukasawa, Tetsuo; Funabashi, Kiyomi; Kondo, Yoshikazu

    1997-08-01

    Silver impregnated alumina adsorbent (AgA), which was developed for iodine removal from off-gas of nuclear power and reprocessing plants has been tested laying emphasis on investigation of the influences gaseous impurities have on adsorbent chemical stability and iodine removal efficiency. The influences of the major impurities such as nitrogen oxides and water vapor were checked on the chemical state of impregnated silver compound (AgNO{sub 3}) and decontamination factor (DF) value. At 150{degrees}C, a forced air flow with 1.5% nitrogen oxide (NO/NO{sub 2}=1/1) reduced silver nitrate to metallic silver, whereas pure air and air with 1.5% NO{sub 2} had no effect on the chemical state of silver. Metallic silver showed a lower DF value for methyl iodide in pure air (without impurities) than silver nitrate and the lower DF of metallic silver was improved when impurities were added. At 40{degrees}C, a forced air flow with 1.5% nitrogen dioxide (NO{sub 2}) increased the AgA weight by about 20%, which was caused by the adsorption of nitric acid solution on the AgA surface. AgA with l0wt% silver showed higher weight increase than that with 24wt% silver which had lower porosity. Adsorption of acid solution lowered the DF value, which would be due to the hindrance of contact between methyl iodide and silver. The influences of other gaseous impurities were also investigated and AgA showed superior characteristics at high temperatures. 14 refs., 11 figs.

  13. Unique properties of silver cations in solid-acid catalysis by zeolites and heteropolyacids.

    PubMed

    Ono, Yoshio; Baba, Toshihide

    2015-06-28

    Ag(+)-exchanged zeolites exhibit unique catalytic properties caused by the combination of their redox and acidic properties. Partial reduction of Ag(+) ions in zeolites with hydrogen leads to the formation of acidic protons and silver metal particles, which can be observed using X-ray powder diffraction patterns (XRD). By simply evacuating hydrogen from the system, the silver metal particles are returned back to Ag(+) ions and at the same time, acidic protons are eliminated. This interconversion of Ag(+) ions and silver metal or gaseous hydrogen and surface protons is reflexed in the catalytic activities of Ag(+)-exchanged zeolites for acid-catalyzed reactions: the activity of Ag(+)-exchanged Y zeolite (Ag-Y) reversibly changes with the partial pressure of hydrogen. Furthermore, the activity of Ag-Y in the presence of hydrogen is higher than that of H(+)-exchanged Y zeolite (H-Y). Similar phenomena are also observed for the silver salt of dodecatungstophosphoric acid (Ag3PW12O40). Ag(+)-exchanged ZSM-5 zeolite (Ag-ZSM-5) is a very selective catalyst for aromatization of alkanes, alkenes and methanol. Examination of the activation step of lower alkanes revealed that Ag(+) ions dramatically enhance the dehydrogenation of the alkanes via heterolytic dissociation of the alkanes into carbenium ions and hydride species. Ag(+)-exchanged zeolites can also activate methane. The reaction of methane with ethene and benzene gives propene and toluene, respectively. Ag-ZSM-5 is a very stable catalyst under hydrothermal conditions because of the interconversion properties of Ag(+) ions and silver metal in the zeolite. PMID:26018842

  14. A silver-alkynyl cluster encapsulating a fluorescent polyoxometalate core: enhanced emission and fluorescence modulation.

    PubMed

    Song, Chao-Yu; Chai, Dong-Feng; Zhang, Rui-Ren; Liu, Hong; Qiu, Yun-Feng; Guo, Hua-Dong; Gao, Guang-Gang

    2015-03-01

    A new silver(I)-alkynyl cluster with a [Eu(W5O18)2](9-) polyoxoanionic core of [Ag42{Eu(W5O18)2}((t)BuC≡C)28Cl4] [OH]·H2O (1) has been designed and synthesized. The [Eu(W5O18)2](9-) polyoxoanion acts as a template to induce the formation of the surrounding 42-core Ag(I) cage. Due to the hydrophobic silver(I)-alkynyl shell, 1 features an unusual fluorescence enhancement as compared to the precursor of the [Eu(W5O18)2](9-) polyoxoanionic core. Interestingly, the silver ions in the shell silver(I)-alkynyl cage can only be reduced to silver atoms by irradiation with high energy UV light (2 kW). Upon high UV irradiation, fluorescence quenching of 1 has been observed. Moreover, the solution fluorescence of 1 can be modulated by addition of S(2-) ions into the system, which also leads to the fluorescence quenching phenomenon. The successful synthesis of 1 demonstrates a new route to the detection of high energy UV irradiation or S(2-) ions by elaborate design of fluorescence quenching of silver(I)-alkynyl clusters. PMID:25612008

  15. Mechanism of silver(I)-assisted growth of gold nanorods and bipyramids.

    PubMed

    Liu, Mingzhao; Guyot-Sionnest, Philippe

    2005-12-01

    The seed-mediated growth of gold nanostructures is shown to be strongly dependent on the gold seed nanocrystal structure. The gold seed solutions can be prepared such that the seeds are either single crystalline or multiply twinned. With added silver(I) in the cetyltrimethylammonium bromide (CTAB) aqueous growth solutions, the two types of seeds yield either nanorods or elongated bipyramidal nanoparticles, in good yields. The gold nanorods are single crystalline, with a structure similar to those synthesized electrochemically (Yu, Y. Y. et al. J. Phys. Chem. B 1997, 101, 6661). In contrast, the gold bipyramids are pentatwinned. These bipyramids are strikingly monodisperse in shape. This leads to the sharpest ensemble longitudinal plasmon resonance reported so far for metal colloid solutions, with an inhomogeneous width as narrow as 0.13 eV for a resonance at approximately 1.5 eV. Ag(I) plays an essential role in the growth mechanism. Ag(I) slows down the growth of the gold nanostructures. Ag(I) also leads to high-energy side facets that are {110} for the single crystalline gold nanorods and unusually highly stepped {11n} (n approximately 7) for the bipyramid. To rationalize these observations, it is proposed that it is the underpotential deposition of Ag(I) that leads to the dominance of the facets with the more open surface structures. This forms the basis for the one-dimensional growth mechanism of single crystal nanorods, while it affects the shape of the nanostructures growing along a single twinning axis. PMID:16853888

  16. Mercuric iodide X-ray camera

    NASA Astrophysics Data System (ADS)

    Patt, B. E.; Delduca, A.; Dolin, R.; Ortale, C.

    A prototype X-ray camera utilizing a 1.5- by 1.5-in., 1024-element, thin mercuric iodide detector array has been tested and evaluated. The microprocessor-based camera is portable and operates at room temperature. Events can be localized within 1 to 2 mm at energies below 60 keV and within 5 to 6 mm at energies on the order of 600 keV.

  17. Mechanical Properties Of Large Sodium Iodide Crystals

    NASA Technical Reports Server (NTRS)

    Lee, Henry M.

    1988-01-01

    Report presents data on mechanical properties of large crystals of thallium-doped sodium iodide. Five specimens in shape of circular flat plates subjected to mechanical tests. Presents test results for each specimen as plots of differential pressure versus center displacement and differential pressure versus stress at center. Also tabulates raw data. Test program also developed procedure for screening candidate crystals for gamma-ray sensor. Procedure eliminates potentially weak crystals before installed and ensures material yielding kept to minimum.

  18. Mercuric iodide X-ray camera

    NASA Astrophysics Data System (ADS)

    Patt, B. E.; del Duca, A.; Dolin, R.; Ortale, C.

    1986-02-01

    A prototype X-ray camera utilizing a 1.5- by 1.5-in., 1024-element, thin mercuric iodide detector array has been tested and evaluated. The microprocessor-based camera is portable and operates at room temperature. Events can be localized within 1-2 mm at energies below 60 keV and within 5-6 mm at energies on the order of 600 keV.

  19. Formation of cyanogen iodide by lactoperoxidase.

    PubMed

    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. PMID:26580225

  20. Composition and properties of thallium mercury iodide

    NASA Astrophysics Data System (ADS)

    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.

  1. Formulation and optimization of potassium iodide tablets

    PubMed Central

    Al-Achi, Antoine; Patel, Binit

    2014-01-01

    The use of potassium iodide (KI) as a protective agent against accidental radioactive exposure is well established. In this study, we aimed to prepare a KI tablet formulation using a direct compression method. We utilized Design of Experiment (DoE)/mixture design to define the best formulation with predetermined physical qualities as to its dissolution, hardness, assay, disintegration, and angle of repose. Based on the results from the DoE, the formulation had the following components (%w/w): Avicel 48.70%, silicon dioxide 0.27%, stearic acid (1.00%), magnesium stearate 2.45%, and dicalcium phosphate 18.69%, in addition to potassium iodide 28.89% (130 mg/tablet). This formulation was scaled-up using two tablet presses, a single-punch press and a rotary mini tablet press. The final scaled-up formulation was subjected to a variety of quality control tests, including photo-stability testing. The results indicate that potassium iodide tablets prepared by a rotary mini tablet press had good pharmaceutical characteristics and a shelf-life of 25 days when stored at room temperature protected from light. PMID:25685048

  2. Formulation and optimization of potassium iodide tablets.

    PubMed

    Al-Achi, Antoine; Patel, Binit

    2015-01-01

    The use of potassium iodide (KI) as a protective agent against accidental radioactive exposure is well established. In this study, we aimed to prepare a KI tablet formulation using a direct compression method. We utilized Design of Experiment (DoE)/mixture design to define the best formulation with predetermined physical qualities as to its dissolution, hardness, assay, disintegration, and angle of repose. Based on the results from the DoE, the formulation had the following components (%w/w): Avicel 48.70%, silicon dioxide 0.27%, stearic acid (1.00%), magnesium stearate 2.45%, and dicalcium phosphate 18.69%, in addition to potassium iodide 28.89% (130 mg/tablet). This formulation was scaled-up using two tablet presses, a single-punch press and a rotary mini tablet press. The final scaled-up formulation was subjected to a variety of quality control tests, including photo-stability testing. The results indicate that potassium iodide tablets prepared by a rotary mini tablet press had good pharmaceutical characteristics and a shelf-life of 25 days when stored at room temperature protected from light. PMID:25685048

  3. Ultrafast Extreme Ultraviolet Spectroscopy of Lead Iodide and Methylammonium Lead Iodide

    NASA Astrophysics Data System (ADS)

    Verkamp, Max; Lin, Ming-Fu; Ryland, Elizabeth; Vura-Weis, Josh

    Methylammonium lead iodide (perovskite) is a leading candidate for use in next-generation solar cell devices. However, the photophysics of perovskite responsible for its strong photovoltaic qualities are not fully understood. Ultrafast extreme ultraviolet (XUV) spectroscopy was used to investigate relaxation dynamics in perovskite and its precursor, lead iodide, with carrier-specific signals arising from transitions from a common inner-shell level (I 4d) to the valence and conduction bands. Ultrashort (30 fs) pulses of XUV radiation in a broad spectrum (40-70 eV) were obtained using high-harmonic generation in a tabletop instrument. Transient absorption measurements with visible pump (3.1 eV) and XUV probe directly observed the relaxation of charge carriers after above band excitation for both perovskite and lead iodide in the femtosecond and picosecond time ranges.

  4. The first trialkylphosphane telluride complexes of Ag(I): molecular, ionic and supramolecular structural alternatives.

    PubMed

    Daniliuc, Constantin; Druckenbrodt, Christian; Hrib, Cristian G; Ruthe, Frank; Blaschette, Armand; Jones, Peter G; du Mont, Wolf-W

    2007-05-28

    The structures of the first phosphane telluride complexes of silver(I), obtained from i-Pr3PTe (1) with AgNMs2 [Ms = SO2CH3] and with AgSbF6, reveal the superior coordinating ability of 1, particularly as a bridging ligand, compared with related i-Pr3PS and i-Pr3PSe ligands. PMID:17713078

  5. Copper-Catalyzed Carboxylation of Aryl Iodides with Carbon Dioxide.

    PubMed

    Tran-Vu, Hung; Daugulis, Olafs

    2013-10-01

    A method for carboxylation of aryl iodides with carbon dioxide has been developed. The reaction employs low loadings of copper iodide/TMEDA or DMEDA catalyst, 1 atm of CO2, DMSO or DMA solvent, and proceeds at 25-70 °C. Good functional group tolerance is observed, with ester, bromide, chloride, fluoride, ether, hydroxy, amino, and ketone functionalities tolerated. Additionally, hindered aryl iodides such as iodomesitylene can also be carboxylated. PMID:24288654

  6. Iodide transport and its regulation in the thyroid gland

    SciTech Connect

    Price, D.J.

    1987-01-01

    This study was undertaken to examine the autoregulatory mechanism of iodide induced suppression of subsequently determined iodide transport activity in the thyroid gland. Two model systems were developed to identify the putative, transport-related, iodine-containing, inhibitory factor responsible for autoregulation. The first system was a maternal and fetal rabbit thyroid tissue slice preparation in which iodide pretreatment inhibited the maternal /sup 125/I-T/M ratio by 30% and had no significant effect on fetal iodide transport. In the second system, the role of protein synthesis in the autoregulatory phenomenon was studied. Cat thyroid slices pretreated with0.1 mM cycloheximide for 60 min prior to preexposure to excess iodide demonstrated a significant reduction in the degree of iodide included autoregulation. In both of these systems iodide induced suppression of cAMP accumulation remained intact. These findings suggest (1) fetal rabbit thyroid lacks the autoregulatory mechanism of iodide transport and (2) protein synthesis is involved in the mechanism of thyroid autoregulation of iodide transport.

  7. EPR and NMR spectroscopies provide input on the coordination of Cu(I) and Ag(I) to a disordered methionine segment.

    PubMed

    Shenberger, Yulia; Gottlieb, Hugo E; Ruthstein, Sharon

    2015-06-01

    Methionine motifs are methionine-rich metal-binding segments found in many human, yeast, and bacterial proteins involved in the transportation of copper ion to other cellular pathways, and in protecting copper from oxidation. Methionine motifs are found to bind Ag(I) and Cu(I) ions. Proteins or peptides that can bind different metal ions should have the ability to differentiate between them, to be able to shuttle them to various pathways in the cell. This study utilizes electron paramagnetic resonance spectroscopy together with circular dichroism and nuclear magnetic resonance to probe structural changes in the methionine segment upon coordinating Cu(I) and Ag(I) metal ions. The data collected here indicate that methionine segments experience structural changes while coordinating Cu(I) and Ag(I), however, the differences between the coordination of Cu(I) vs. Ag(I) to the methionine segment are mild. Since Cu(I) and Ag(I) metal ions are pretty similar in their nature and charge, the minor structural changes reported here are significant towards the understanding of the differences in the transport mechanism of these two metal ions in prokaryotic and eukaryotic cells. PMID:25822808

  8. Antimicrobial characteristic of insoluble alkylpyridinium iodide.

    PubMed Central

    Nakagawa, Y; Yamano, Y; Tawaratani, T; Kourai, H; Horie, T; Shibasaki, I

    1982-01-01

    Insoluble and soluble alkylpyridinium iodides (C8 to C18) were synthesized. The insoluble agents were quaternized 4-vinylpyridine-divinylbenzene copolymers. The insoluble agent [C12(50)] that contained 50% divinylbenzene and had a C12 alkyl chain was selected as the most suitable insoluble agent. C12(50) showed poor durability of the antibacterial activity, but C12(50), which had lost the activity, was refreshed by washing with ethanol. This washing became ineffective after a few cycles of antibacterial treatment and refreshment. Such C12(50) recovered the activity upon 1.0 N NaOH treatment. The antibacterial activity of C12(50) depended on its surface area. It showed high antimicrobial activity against gram-positive bacteria and also showed activity against gram-negative bacteria and yeasts. But the activities of C12(50) and laurylpyridinium iodide solution were different against some microbes. The antibacterial activities of the agents were investigated against Escherichia coli and Micrococcus luteus under various conditions. The activity of C12(50) was higher at a higher temperature or at a lower cell concentration. The activity of C12(50) decreased on addition of NaCl, glucose, or bovine albumin to the cell suspension or in 0.01 M sodium-potassium phosphate buffer. C12(50) showed less activity when cells were mixed with dead cells or the supernatant of dead cells killed in an autoclave. The mode of action of the laurylpyridinium iodide solution against E. coli and M. luteus was similar to that of C12(50) except for the influence of E. coli cell concentration. PMID:6808918

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

    PubMed

    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. PMID:26745029

  10. Large-area mercuric iodide photodectors

    NASA Astrophysics Data System (ADS)

    Markakis, J.; Ortale, C.; Schnepple, W.; Iwanczyk, J.; Dabrowski, A.

    1983-07-01

    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 are discussed. 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.

  11. Recent developments in thick mercuric iodide spectrometers

    NASA Astrophysics Data System (ADS)

    Hull, K.; Beyerle, A.; Lopez, B.; Markakis, J.; Ortale, C.; Schnepple, W.; Vandenberg, L.

    Thick (approx. 1 cm) mercuric iodide gamma-ray detectors have been produced which show spectroscopic qualities at moderate detector biases (approx. 5 kV) comparable to those of thin spectrometers. Efficiency measurements indicate that the entire volume of the detectors is active. Spectra resolutions of less than 10% have been obtained for gamma-ray energies above 1 MeV. Short charge collection times have produced the best results. Measurement of crystal charge transport properties is discussed. A small amount of bias conditioning is necessary for best performance. Operating parameters of the detectors have been investigated.

  12. Mechanochromic luminescence of copper iodide clusters.

    PubMed

    Benito, Quentin; Maurin, Isabelle; Cheisson, Thibaut; Nocton, Gregory; Fargues, Alexandre; Garcia, Alain; Martineau, Charlotte; Gacoin, Thierry; Boilot, Jean-Pierre; Perruchas, Sandrine

    2015-04-01

    Luminescent mechanochromic materials are particularly appealing for the development of stimuli-responsive materials. Establishing the mechanism responsible for the mechanochromism is always an issue owing to the difficulty in characterizing the ground phase. Herein, the study of real crystalline polymorphs of a mechanochromic and thermochromic luminescent copper iodide cluster permits us to clearly establish the mechanism involved. The local disruption of the crystal packing induces changes in the cluster geometry and in particular the modification of the cuprophilic interactions, which consequently modify the emissive states. This study constitutes a step further toward the understanding of the mechanism involved in the mechanochromic luminescent properties of multimetallic coordination complexes. PMID:25755012

  13. The addition of iodine to tetramethylammonium iodide

    USGS Publications Warehouse

    Foote, H.W.; Fleischer, M.

    1953-01-01

    The system tetramethylammonium iodide-iodine-toluene has been studied by the solubility method at 6 and at 25??. The compounds (CH3)4NI3, (CH3)4NI5 and (CH3)4NI11 were found to be stable phases at both temperatures. In addition, the compound (CH3)4NI10 was found at 6?? and the compound (CH3)4NI9 at 25??. The dissociation pressures of the compounds at these temperatures were calculated from the solubility data.

  14. Europium-doped barium bromide iodide

    SciTech Connect

    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.

  15. Three new Ag(I) coordination architectures based on mixed ligands: Syntheses, structures and photoluminescent properties

    SciTech Connect

    Li, Yamin; Xiao, Changyu; Li, Shu; Chen, Qi; Li, Beibei; Liao, Qian; Niu, Jingyang

    2013-04-15

    Three new silver (I) coordination complexes, [Ag{sub 2}(1,2-bdc)(phdat)]{sub n} (1), [Ag{sub 2}(NO{sub 2}-bdc)(phdat)]{sub n} (2), [Ag{sub 4}(nta){sub 3}(phdat)NO{sub 3}]{sub n} (3) (1,2-bdc=phthalic acid dianion, NO{sub 2}-bdc=5-nitro-1,3-benzenedicarboxylic acid dianion, nta=nicotinic acid anion, phdat=2,4-diamine-6-phenyl-1,3,5-triazine) have been hydrothermally synthesized by the reactions of silver nitrate and phdat with the homologous ligands 1,2-H{sub 2}bdc, NO{sub 2}-H{sub 2}bdc, and Hnta, respectively, and characterized by single-crystal X-ray diffractions, IR spectra, elemental analyses thermogravimetric analyses (TGA). The compound 1 exhibits a chiral 3D network with cbs/CrB self-dual topological net, which contains two kinds of single helical chains. For compound 2, the 3D network is comprised of two kinds of similar 2D sheets with the topological symbol of sql-type packed in AABBAA mode by Ag–N/O weakly contacts. And compound 3 has 2D double layer architecture, consisting of the 2D plane with hcb-type topological symbol connected by Ag–O weakly coordinations. The photoluminescent properties associated with the crystal structures of three compounds have also been measured. - Graphical abstract: Three new silver(I) coordination complexes 1–3 have been synthesized and characterized by single-crystal X-ray diffractions, IR spectra, elemental analyses, thermogravimetric analyses (TGA) and photoluminescent spectra. Highlights: ► The compound 1 exhibits a novel chiral 3D network with two kinds of single helical chains. ► 3D or 2D new Ag coordination complexes. ► The photoluminescent properties have been measured.

  16. Phase 2 Methyl Iodide Deep-Bed Adsorption Tests

    SciTech Connect

    Soelberg, Nick; Watson, Tony

    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.

  17. catena-Poly[[(benzoato-kappaO)silver(I)]-mu-2-aminopyrimidine-kappa2N1:N3].

    PubMed

    You, Zhong Lu; Zhu, Hai Liang

    2004-12-01

    The title complex, [Ag(C(7)H(5)O(2))(C(4)H(5)N(3))](n), is a polymer based on a mononuclear silver(I)-centered fragment. The Ag(I) atom is trigonally coordinated by two N atoms from two 2-aminopyrimidine ligands and one O atom from one benzoate anion, giving zigzag polymeric chains with an [-Ag-N-C-N-](n) backbone running along the a axis. It is proposed that intermolecular hydrogen bonding drives the formation of the chain polymer. PMID:15579946

  18. A Raman spectroscopic and electrochemical study of the photoinduced crystallization of triethylenediamine triiodide upon a silver electrode

    NASA Astrophysics Data System (ADS)

    Ozek, Toru; Irish, Donald E.

    1991-02-01

    When a silver electrode, electrochemically coated with AgI, is immersed in an electrolyte containing NaI and the diprotonated form of 1,4-diazabicyclo 2.2.2 octane (abbreviated DABCO-H22+), and is bathed in 514.5 nm radiation from an argon ion laser through the objective of the microscope attachment of the DILOR Omars-89 Raman spectrophotometer, crystals form from the focal point. These are attributed to DABCO-h22+ 213-. Both spectroscopic and electrochemical experiments are described and interrelated. A mechanism for this photoinduced electrochemical crystal growth is presented.

  19. Silver nanowires

    NASA Astrophysics Data System (ADS)

    Graff, A.; Wagner, D.; Ditlbacher, H.; Kreibig, U.

    2005-07-01

    Free silver nanowires were produced in aqueous electrolyte by a novel chemical reaction. Their diameters are about 27 nm, the lengths range up to more than 70 μm, yielding extreme length to thickness-ratios up to 2500. Their structure was identified by TEM analysis (SAED) and HRTEM to consist of a lattice aligned bundle of five monocrystalline rods of triangular cross-section forming an almost regular pentagonal cross-section. It is demonstrated that, for application purposes, single free nanowires can be mounted between contact areas. This manipulation is enabled by observing the nanowires in real time at atmosphere by Zsigmondy-Siedentopf farfield darkfield microscopy. Experimental results are presented concerning electrical dc conductivity and optical plasmon polariton excitation, the latter obtained from a single free wire without substrate and a single wire deposited on quartz glass. We also report about a present research cooperation with the Graz group of Aussenegg and Krenn which is devoted to investigate plasmon propagation in our Ag nanowires and to prove application possibilities as information guide fibers in analogy to optical fibers which may be integrated into micro- and nanoelectronic circuits.

  20. The Silver Halides

    ERIC Educational Resources Information Center

    Sahyun, M. R. V.

    1977-01-01

    Illustrates the type of fractional bonding for solid silver halides. Treats the silver halides as electron excess compounds, and develops a model of a localized bonding unit that may be iterated in three dimensions to describe the bulk phase. (MLH)

  1. Colloidal Silver Products

    MedlinePlus

    ... can be dangerous to your health. What the Science Says About the Safety and Side Effects of ... homemade and commercial colloidal silver products. What the Science Says About the Effectiveness of Colloidal Silver Scientific ...

  2. 21 CFR 520.763 - Dithiazanine iodide oral dosage forms.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Dithiazanine iodide oral dosage forms. 520.763 Section 520.763 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES... Dithiazanine iodide oral dosage forms....

  3. Iodide sensing via electrochemical etching of ultrathin gold films

    NASA Astrophysics Data System (ADS)

    Dielacher, Bernd; Tiefenauer, Raphael F.; Junesch, Juliane; Vörös, János

    2015-01-01

    Iodide is an essential element for humans and animals and insufficient intake is still a major problem. Affordable and accurate methods are required to quantify iodide concentrations in biological and environmental fluids. A simple and low cost sensing device is presented which is based on iodide induced electrochemical etching of ultrathin gold films. The sensitivity of resistance measurements to film thickness changes is increased by using films with a thickness smaller than the electron mean free path. The underlying mechanism is demonstrated by simultaneous cyclic voltammetry experiments and resistance change measurements in a buffer solution. Iodide sensing is conducted in buffer solutions as well as in lake water with limits of detection in the range of 1 μM (127 μg L-1) and 2 μM (254 μg L-1), respectively. In addition, nanoholes embedded in the thin films are tested for suitability of optical iodide sensing based on localized surface plasmon resonance.

  4. Optimization of silver-dielectric-silver nanoshell for sensing applications

    SciTech Connect

    Shirzaditabar, Farzad; Saliminasab, Maryam

    2013-08-15

    In this paper, resonance light scattering (RLS) properties of a silver-dielectric-silver nanoshell, based on quasi-static approach and plasmon hybridization theory, are investigated. Scattering spectrum of silver-dielectric-silver nanoshell has two intense and clearly separated RLS peaks and provides a potential for biosensing based on surface plasmon resonance and surface-enhanced Raman scattering. The two RLS peaks in silver-dielectric-silver nanoshell are optimized by tuning the geometrical dimensions. In addition, the optimal geometry is discussed to obtain the high sensitivity of silver-dielectric-silver nanoshell. As the silver core radius increases, the sensitivity of silver-dielectric-silver nanoshell decreases whereas increasing the middle dielectric thickness increases the sensitivity of silver-dielectric-silver nanoshell.

  5. Dry method for recycling iodine-loaded silver zeolite

    DOEpatents

    Thomas, Thomas R.; Staples, Bruce A.; Murphy, Llewellyn P.

    1978-05-09

    Fission product iodine is removed from a waste gas stream and stored by passing the gas stream through a bed of silver-exchanged zeolite until the zeolite is loaded with iodine, passing dry hydrogen gas through the bed to remove the iodine and regenerate the bed, and passing the hydrogen stream containing the hydrogen iodide thus formed through a lead-exchanged zeolite which adsorbs the radioactive iodine from the gas stream and permanently storing the lead-exchanged zeolite loaded with radioactive iodine.

  6. Carrier traps and transport in mercuric iodide

    NASA Astrophysics Data System (ADS)

    Schlesinger, T. E.; Bao, X. J.; James, R. B.; Cheng, A. Y.; Ortale, C.; van den Berg, L.

    1992-11-01

    Thermally stimulated current spectroscopy (TSC) was performed on a variety of mercuric iodide samples and detectors to determine the nature and origin of deep traps in this material. It is shown that the trap type and concentration is a function of the metal overlayer employed as a contact material. The energy barrier height as well as the type (electron or hole) of barrier at the metal/semiconductor interface has also been determined by internal photoemission measurements. When polarization effects are not present, as is the case in most Pd contacted samples, the barrier height can be accurately determined by this technique. A value of 1.05 eV was measured for a hole barrier at the Pd/Hgl 2 interface.

  7. Silver(I) Ions Ultrasensitive Detection at Carbon Electrodes—Analysis of Waters, Tobacco Cells and Fish Tissues

    PubMed Central

    Krizkova, Sona; Krystofova, Olga; Trnkova, Libuse; Hubalek, Jaromir; Adam, Vojtech; Beklova, Miroslava; Horna, Ales; Havel, Ladislav; Kizek, Rene

    2009-01-01

    We used carbon paste electrodes and a standard potentiostat to detect silver ions. The detection limit (3 Signal/Noise ratio) was estimated as 0.5 μM. A standard electrochemical instrument microanalysis of silver(I) ions was suggested. As a working electrode a carbon tip (1 mL) or carbon pencil was used. Limits of detection estimated by dilution of a standard were 1 (carbon tip) or 10 nM (carbon pencil). Further we employed flow injection analysis coupled with carbon tip to detect silver(I) ions released in various beverages and mineral waters. During first, second and third week the amount of silver(I) ions releasing into water samples was under the detection limit of the technique used for their quantification. At the end of a thirteen weeks long experiment the content of silver(I) ions was several times higher compared to the beginning of release detected in the third week and was on the order of tens of nanomoles. In subsequent experiments the influence of silver(I) ions (0, 5 and 10 μM) on a plant model system (tobacco BY-2 cells) during a four-day exposition was investigated. Silver(I) ions were highly toxic to the cells, which was revealed by a double staining viability assay. Moreover we investigated the effect of silver(I) ions (0, 0.3, 0.6, 1.2 and 2.5 μM) on guppies (Poecilia reticulata). Content of Ag(I) increased with increasing time of the treatment and applied concentrations in fish tissues. It can be concluded that a carbon tip or carbon pencil coupled with a miniaturized potentiostat can be used for detection of silver(I) ions in environmental samples and thus represents a small, portable, low cost and easy-to-use instrument for such purposes. PMID:22399980

  8. Stacks and clips: Uncanny similarities in the modes of self-assembly in tenary Ag(I) complexes with 1,2-diazines and chelating heteroarenes

    PubMed Central

    Türkmen, Yunus E.; Sen, Saikat

    2014-01-01

    The first synthesis and structural elucidation of Ag(I) ternary complexes with 1,2-diazines and chelating heteroarenes have been described. Conserved modes of inter-cation Ag+⋯π and π⋯π stacking interactions result in near identical patterns of cation self-assembly in these ternary complexes. PMID:24701132

  9. Meeting the 2020 American Graduation Initiative (AGI) Goal of Increasing Postsecondary Graduation Rates and Completions: A Macro Perspective of Community College Student Educational Attainment

    ERIC Educational Resources Information Center

    Kotamraju, Pradeep; Blackman, Orville

    2011-01-01

    The paper uses the Integrated Postsecondary Education Data system (IPEDS) data to simulate the 2020 American Graduation Initiative (AGI) goal introduced by President Obama in the summer of 2009. We estimate community college graduation rates and completion numbers under different scenarios that include the following sets of variables: (a) internal…

  10. Flavonoid Rutin Increases Thyroid Iodide Uptake in Rats

    PubMed Central

    Lima Gonçalves, Carlos Frederico; de Souza dos Santos, Maria Carolina; Ginabreda, Maria Gloria; Soares Fortunato, Rodrigo; Pires de Carvalho, Denise; Freitas Ferreira, Andrea Claudia

    2013-01-01

    Thyroid iodide uptake through the sodium-iodide symporter (NIS) is not only an essential step for thyroid hormones biosynthesis, but also fundamental for the diagnosis and treatment of different thyroid diseases. However, part of patients with thyroid cancer is refractory to radioiodine therapy, due to reduced ability to uptake iodide, which greatly reduces the chances of survival. Therefore, compounds able to increase thyroid iodide uptake are of great interest. It has been shown that some flavonoids are able to increase iodide uptake and NIS expression in vitro, however, data in vivo are lacking. Flavonoids are polyhydroxyphenolic compounds, found in vegetables present in human diet, and have been shown not only to modulate NIS, but also thyroperoxidase (TPO), the key enzyme in thyroid hormones biosynthesis, besides having antiproliferative effect in thyroid cancer cell lines. Therefore, we aimed to evaluate the effect of some flavonoids on thyroid iodide uptake in Wistar rats in vivo. Among the flavonoids tested, rutin was the only one able to increase thyroid iodide uptake, so we decided to evaluate the effect of this flavonoid on some aspects of thyroid hormones synthesis and metabolism. Rutin led to a slight reduction of serum T4 and T3 without changes in serum thyrotropin (TSH), and significantly increased hypothalamic, pituitary and brown adipose tissue type 2 deiodinase and decreased liver type 1 deiodinase activities. Moreover, rutin treatment increased thyroid iodide uptake probably due to the increment of NIS expression, which might be secondary to increased response to TSH, since TSH receptor expression was increased. Thus, rutin might be useful as an adjuvant in radioiodine therapy, since this flavonoid increased thyroid iodide uptake without greatly affecting thyroid function. PMID:24023911

  11. Imaging the heterogeneity of mineral surface reactivity using Ag(I) and synchrotron X-ray microscopy

    SciTech Connect

    Amonette, James E.; Heald, Steve M.; Russell, Colleen K.

    2003-10-01

    Microscopic-scale imaging of reduced zones on the surfaces of minerals can be achieved by reaction with dilute Ag(I) solutions and subsequent analysis using synchrotron X-ray microscopy (XRM) above the Ag K-edge (25.5 keV). The principal reductant is Fe(II), but other reductants such as sulfide may contribute. Reduced zones may exist instrinsically, as in the structure of biotite and augite, or may be generated by reaction with chemical agents such as dithionite or treatment with sulfate-reducing bacteria (SRB). We demonstrate the method on flakes of specular hematite and biotite, as well as on thin sections of different rocks (arfvedsonitic granite, oolitic hematite, diabase, and quartz conglomerate) treated with SRB, and discuss possible artifacts that can occur. To our knowledge, this is the only microscopic technique that can image Fe(II) zones on the surface of an Fe-bearing mineral with monolayer sensitivity.

  12. Syntheses and characterization of AgI nano-structures by ultrasonic method: Different morphologies under different conditions.

    PubMed

    Abbasi, Amir Reza; Morsali, Ali

    2010-03-01

    Nano-structures of AgI have been prepared by reaction between AgNO(3) and KI under ultrasound irradiation. Some of parameters such as effect of stirring, temperature, sonicating time in growth and morphology of the nano-structures have been studied. The sizes distributions depend slighter on reaction conditions. But, morphology of nano-structure depends strongly on reaction parameters. With change of solvent concentration and sonicating time, nanoparticles structures changed to nanowires. An increasing of temperature results in an increasing of solubility. As a result, nuclei with small sizes become unstable and dissolve back into the solution. Attendance or non-attendance of stirring is another parameter that effects on morphology of nano-structures. In some conditions, non-attendance of stirring led to nanowires structure and in the other conditions, nanoparticles structures were prepared. The samples were characterized with powder X-ray diffraction (XRD), scanning electron microscopy (SEM). PMID:19959390

  13. Silver Accumulation in the Green Microalga Coccomyxa actinabiotis: Toxicity, in Situ Speciation, and Localization Investigated Using Synchrotron XAS, XRD, and TEM.

    PubMed

    Leonardo, Thomas; Farhi, Emmanuel; Pouget, Stéphanie; Motellier, Sylvie; Boisson, Anne-Marie; Banerjee, Dipanjan; Rébeillé, Fabrice; den Auwer, Christophe; Rivasseau, Corinne

    2016-01-01

    Microalgae are good candidates for toxic metal remediation biotechnologies. This study explores the cellular processes implemented by the green microalga Coccomyxa actinabiotis to take up and cope with silver over the concentration range of 10(-7) to 10(-2) M Ag(+). Understanding these processes enables us to assess the potential of this microalga for applications for bioremediation. Silver in situ speciation and localization were investigated using X-ray absorption spectroscopy, X-ray diffraction, and transmission electron microscopy. Silver toxicity was evaluated by monitoring microalgal growth and photochemical parameters. Different accumulation mechanisms were brought out depending on silver concentration. At low micromolar concentration, microalgae fixed all silver initially present in solution, trapping it inside the cells into the cytosol, mainly as unreduced Ag(I) bound with molecules containing sulfur. Silver was efficiently detoxified. When concentration increased, silver spread throughout the cell and particularly entered the chloroplast, where it damaged the photosystem. Most silver was reduced to Ag(0) and aggregated to form crystalline silver nanoparticles of face-centered cubic structure with a mean size of 10 nm. An additional minor interaction of silver with molecules containing sulfur indicated the concomitant existence of the mechanism observed at low concentration or nanoparticle capping. Nanoparticles were observed in chloroplasts, in mitochondria, on the plasma membrane, on cytosolic membrane structures, and in vacuoles. Above 10(-4) M Ag(+), damages were irreversible, and photosynthesis and growth were definitely inhibited. However, high silver amounts remained confined inside microalgae, showing their potential for the bioremediation of contaminated water. PMID:26606242

  14. Tolerance to silver of an Aspergillus fumigatus strain able to grow on cyanide containing wastes.

    PubMed

    Sabatini, L; Battistelli, M; Giorgi, L; Iacobucci, M; Gobbi, L; Andreozzi, E; Pianetti, A; Franchi, R; Bruscolini, F

    2016-04-01

    We studied the strategy of an Aspergillus fumigatus strain able to grow on metal cyanide wastes to cope with silver. The tolerance test revealed that the Minimum Inhibitory Concentration of Ag(I) was 6mM. In 1mM AgNO3 aqueous solution the fungus was able to reduce and sequestrate silver into the cell in the form of nanoparticles as evidenced by the change in color of the biomass and Electron Microscopy observations. Extracellular silver nanoparticle production also occurred in the filtrate solution after previous incubation of the fungus in sterile, double-distilled water for 72h, therefore evidencing that culture conditions may influence nanoparticle formation. The nanoparticles were characterized by UV-vis spectrometry, X-ray diffraction and Energy Dispersion X-ray analysis. Atomic absorption spectrometry revealed that the optimum culture conditions for silver absorption were at pH 8.5.The research is part of a polyphasic study concerning the behavior of the fungal strain in presence of metal cyanides; the results provide better understanding for further research targeted at a rationale use of the microorganism in bioremediation plans, also in view of possible metal recovery. Studies will be performed to verify if the fungus maintains its ability to produce nanoparticles using KAg(CN)2. PMID:26705888

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

    PubMed

    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 < 0.05 vs. 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

  16. Silver and Gold NMR

    PubMed Central

    Zangger, Klaus

    1999-01-01

    Silver and gold, together with copper, form the transition metal group IB elements in the periodic table and possess very different nuclear magnetic resonance (NMR) spectroscopic properties. While there is only one gold isotope (197Au), which has a spin of 3/2 and therefore a quadrupole moment, silver occurs in two isotopic forms (109Ag and 109Au), both of which have a spin 1/2 and similar NMR spectroscopic properties. The unfavorable properties of gold have prevented its NMR spectroscopic investigation thus far. On the other hand, there are several reports of silver NMR. However, the low sensitivity of silver, combined with its long relaxation times have rendered the direct detection of silver possible only with concentrations greater than a few tenth molar. Reviewed here are the general limitations of silver NMR and some techniques to partially overcome these limitations, as well as a summary of currently available chemical shift and scalar coupling data on 109Ag. PMID:18475898

  17. Genetics Home Reference: Silver syndrome

    MedlinePlus

    ... Me Understand Genetics Home Health Conditions Silver syndrome Silver syndrome Enable Javascript to view the expand/collapse boxes. Download PDF Open All Close All Description Silver syndrome belongs to a group of genetic disorders ...

  18. Synthesis and Anticancer Properties of Silver(I) Complexes Containing 2,6-Bis(substituted)pyridine Derivatives

    PubMed Central

    Ali, Korany A.; Abd-Elzaher, Mokhles M.; Mahmoud, Khaled

    2013-01-01

    Several new 2,6-bis(substituted)pyridine ligands and 2,6-bis(substituted)pyridine Ag(I) nitrate complexes were synthesized and characterized spectroscopically. The newly synthesized ligands include pyridine-2,6-bis(3-oxopropanenitrile) (1), pyridine-2,6-bis(2-cyano-N-phenyl-3-oxopropanethioamide) (2), and pyridine-2,6-bis((E)-2-(2-phenylhydrazono)-3-oxopropanenitrile) (3). The newly synthesized ligands and silver(I) complexes were evaluated for their in vitro anticancer activity against four human cancer cell lines including hepatocellular carcinoma (HePG2), lung adenocarcinoma (A549), colon carcinoma (HT29), and breast adenocarcinoma (MCF7). Most of the newly synthesized silver(I) complexes exhibited better activity than the ligands, and the results have been compared with doxorubicin as a reference drug. PMID:25386361

  19. Preparation and evaluation of mercuric iodide for crystal growth

    NASA Astrophysics Data System (ADS)

    Skinner, N. L.; Ortale, C.; Schieber, M. M.; Vandenberg, L.

    Large quantities, on the order of several hundred, of consistent, high quality mercuric iodide for crystal growth have not been commercially available. The hydrocarbon, anion, and cation impurity levels varied considerably, occasionally preventing crystal growth. This occurred even though the starting materials was from the same vendor and was subjected to the same purification treatment. This paper will describe an aqueous precipitation process of mercuric iodide preparation in batches of 3 kg using Hg(NO sub 3) sub 2, or HgCl and KI. Since these salts are produced in much larger quantities than mercuric iodide, more consistent quality is available. The impurity content of these batched and single crystals are compared. Some of the single crystals grown using the in-house prepared mercuric iodide have yielded a large number of spectroscopy grade nuclear radiation detectors. The influence of the major impurities are discussed.

  20. Laboratory measurements of parameters affecting wet deposition of methyl iodide

    SciTech Connect

    Maeck, W.J.; Honkus, R.J.; Keller, J.H.; Voilleque, P.G.

    1984-09-01

    The transfer of gaseous methyl iodide (CH/sub 3/I) to raindrops and the initial retention by vegetation of CH/sub 3/I in raindrops have been studied in a laboratory experimental program. The measured air-to-drop transfer parameters and initial retention factors both affect the wet deposition of methyl iodide onto vegetation. No large effects on the air-to-drop transfer due to methyl iodide concentration, temperature, acidity, or rain type were observed. Differences between laboratory measurements and theoretical values of the mass transfer coefficient were found. Pasture grass, lettuce, and alfalfa were used to study the initial retention of methyl iodide by vegetation. Only a small fraction of the incident CH/sub 3/I in raindrops was held by any of the three vegetation types.

  1. Dosimetry using silver salts

    DOEpatents

    Warner, Benjamin P.

    2003-06-24

    The present invention provides a method for detecting ionizing radiation. Exposure of silver salt AgX to ionizing radiation results in the partial reduction of the salt to a mixture of silver salt and silver metal. The mixture is further reduced by a reducing agent, which causes the production of acid (HX) and the oxidized form of the reducing agent (R). Detection of HX indicates that the silver salt has been exposed to ionizing radiation. The oxidized form of the reducing agent (R) may also be detected. The invention also includes dosimeters employing the above method for detecting ionizing radiation.

  2. Structural diversity in hybrid organic-inorganic lead iodide materials.

    PubMed

    Weber, Oliver J; Marshall, Kayleigh L; Dyson, Lewis M; Weller, Mark T

    2015-12-01

    The structural chemistry of hybrid organic-inorganic lead iodide materials has become of increasing significance for energy applications since the discovery and development of perovskite solar cells based on methylammonium lead iodide. Seven new hybrid lead iodide compounds have been synthesized and structurally characterized using single-crystal X-ray diffraction. The lead iodide units in materials templated with bipyridyl, 1,2-bis(4-pyridyl)ethane, 1,2-di(4-pyridyl)ethylene and imidazole adopt one-dimensional chain structures, while crystallization from solutions containing piperazinium cations generates a salt containing isolated [PbI6](4-) octahedral anions. Templating with 4-chlorobenzylammonium lead iodide adopts the well known two-dimensional layered perovskite structure with vertex shared sheets of composition [PbI4](2-) separated by double layers of organic cations. The relationships between the various structures determined, their compositions, stability and hydrogen bonding between the protonated amine and the iodide ions of the PbI6 octahedra are described. PMID:26634723

  3. Potassium Iodide ("KI"): Instructions to Make Potassium Iodide Solution for Use During a Nuclear Emergency (Liquid Form)

    MedlinePlus

    ... make Potassium Iodide Solution for Use During a Nuclear Emergency (Liquid Form) Share Tweet Linkedin Pin it ... Preparation and Dosing Instructions for Use During a Nuclear Emergency To Make KI Solution (Liquid Form), using ...

  4. The silver ions contribution into the cytotoxic activity of silver and silver halides nanoparticles

    NASA Astrophysics Data System (ADS)

    Klimov, A. I.; Zherebin, P. M.; Gusev, A. A.; Kudrinskiy, A. A.; Krutyakov, Y. A.

    2015-11-01

    The biocidal action of silver nanoparticles capped with sodium citrate and silver halides nanoparticles capped with non-ionic surfactant polyoxyethylene(20)sorbitan monooleate (Tween 80®) against yeast cells Saccharomyces cerevisiae was compared to the effect produced by silver nitrate and studied through the measurement of cell loss and kinetics of K+ efflux from the cells. The cytotoxicity of the obtained colloids was strongly correlated with silver ion content in the dispersions. The results clearly indicated that silver and silver halides nanoparticles destroyed yeast cells through the intermediate producing of silver ions either by dissolving of salts or by oxidation of silver.

  5. Posttranscriptional regulation of sodium-iodide symporter mRNA expression in the rat thyroid gland by acute iodide administration.

    PubMed

    Serrano-Nascimento, Caroline; Calil-Silveira, Jamile; Nunes, Maria Tereza

    2010-04-01

    Iodide is an important regulator of thyroid activity. Its excess elicits the Wolff-Chaikoff effect, characterized by an acute suppression of thyroid hormone synthesis, which has been ascribed to serum TSH reduction or TGF-beta increase and production of iodolipids in the thyroid. These alterations take hours/days to occur, contrasting with the promptness of Wolff-Chaikoff effect. We investigated whether acute iodide administration could trigger events that precede those changes, such as reduction of sodium-iodide symporter (NIS) mRNA abundance and adenylation, and if perchlorate treatment could counteract them. Rats subjected or not to methylmercaptoimidazole treatment (0.03%) received NaI (2,000 microg/0.5 ml saline) or saline intraperitoneally and were killed 30 min up to 24 h later. Another set of animals was treated with iodide and perchlorate, in equimolar doses. NIS mRNA content was evaluated by Northern blotting and real-time PCR, and NIS mRNA poly(A) tail length by rapid amplification of cDNA ends-poly(A) test (RACE-PAT). We observed that NIS mRNA abundance and poly(A) tail length were significantly reduced in all periods of iodide treatment. Perchlorate reversed these effects, indicating that iodide was the agent that triggered the modifications observed. Since the poly(A) tail length of mRNAs is directly associated with their stability and translation efficiency, we can assume that the rapid decay of NIS mRNA abundance observed was due to a reduction of its stability, a condition in which its translation could be impaired. Our data show for the first time that iodide regulates NIS mRNA expression at posttranscriptional level, providing a new mechanism by which iodide exerts its autoregulatory effect on thyroid. PMID:20107044

  6. Engineering and design properties of thallium-doped sodium iodide and selected properties of sodium-doped cesium iodide

    NASA Technical Reports Server (NTRS)

    Forrest, K.; Haehner, C.; Heslin, T.; Magida, M.; Uber, J.; Freiman, S.; Hicho, G.; Polvani, R.

    1984-01-01

    Mechanical and thermal properties, not available in the literature but necessary to structural design, using thallium doped sodium iodide and sodium doped cesium iodide were determined to be coefficient of linear thermal expansion, thermal conductivity, thermal shock resistance, heat capacity, elastic constants, ultimate strengths, creep, hardness, susceptibility to subcritical crack growth, and ingot variation of strength. These properties were measured for single and polycrystalline materials at room temperature.

  7. Modulation of the Structure and Properties of Uranyl Ion Coordination Polymers Derived from 1,3,5-Benzenetriacetate by Incorporation of Ag(I) or Pb(II).

    PubMed

    Thuéry, Pierre; Harrowfield, Jack

    2016-07-01

    Reaction of uranyl nitrate with 1,3,5-benzenetriacetic acid (H3BTA) in the presence of additional species, either organic bases or their conjugate acids or metal cations, has provided 12 new crystalline complexes, all but one obtained under solvo-hydrothermal conditions. The complexes [C(NH2)3][UO2(BTA)]·H2O (1) and [H2NMe2][UO2(BTA)] (2) crystallize as one- or two-dimensional (1D or 2D) assemblies, respectively, both with uranyl tris-chelation by carboxylate groups and hydrogen-bonded counterions but different ligand conformations. One of the bound carboxylate units is replaced by chelating 1,10-phenanthroline (phen) or 3,4,7,8-tetramethyl-1,10-phenanthroline (Me4phen) in the complexes [(UO2)3(BTA)2(phen)3]·4H2O (3) and [(UO2)3(BTA)2(Me4phen)3]·NMP·3H2O (4) (NMP = N-methyl-2-pyrrolidone), which are a 2D network with honeycomb topology and a 1D polymer, respectively. With silver(I) cations, [UO2Ag(BTA)] (5), a three-dimensional (3D) framework in which the ligand assumes various chelating/bridging coordination modes, and the aromatic ring is involved in Ag(I) bonding, is obtained. A series of seven heterometallic complexes results when lead(II) cations and N-chelating molecules are both present. The complexes [UO2Pb(BTA)(NO3)(bipy)] (6) and [UO2Pb2(BTA)2(bipy)2]·3H2O (7), where bipy is 2,2'-bipyridine, crystallize from the one solution, as 1D and 2D assemblies, respectively. The two 1D coordination polymers [UO2Pb(BTA)(HCOO)(phen)] (8 and 9), again obtained from the one synthesis, provide an example of coordination isomerism, with the formate anion bound either to lead(II) or to uranyl cations. Another 2D architecture is found in [(UO2)2Pb2(BTA)2(HBTA)(H2O)2(phen)2]·2H2O (10), which provides a possible example of a Pb-oxo(uranyl) "cation-cation" interaction. While [UO2Pb(BTA)(HCOO)0.5(NO3)0.5(Me2phen)] (11), where Me2phen is 5,6-dimethyl-1,10-phenanthroline, is a 1D assembly close to those in 6 and 8, [UO2Pb2(BTA)2(Me4phen)2] (12), obtained together with

  8. The Silver Bullet Syndrome.

    ERIC Educational Resources Information Center

    Dehne, George C.

    1995-01-01

    Many colleges address complex problems with a single "silver bullet" strategy. Because value shifts according to the consumer's situation or goal, private colleges should become more aware of their "situational value" and exploit it. This requires an understanding of how students choose colleges. In contrast, popular silver bullets target…

  9. Method for the recovery of silver from silver zeolite

    DOEpatents

    Reimann, G.A.

    1985-03-05

    High purity silver is recovered from silver exchanged zeolite used to capture radioactive iodine from nuclear reactor and nuclear fuel reprocessing environments. The silver exchanged zeolite is heated with slag formers to melt and fluidize the zeolite and release the silver, the radioactivity removing with the slag. The silver containing metallic impurities is remelted and treated with oxygen and a flux to remove the metal impurities. About 98% of the silver in the silver exchanged zeolite having a purity of 99% or better is recoverable by the method.

  10. Method for the recovery of silver from silver zeolite

    SciTech Connect

    Reimann, George A.

    1986-01-01

    High purity silver is recovered from silver exchanged zeolite used to capture radioactive iodine from nuclear reactor and nuclear fuel reprocessing environments. The silver exchanged zeolite is heated with slag formers to melt and fluidize the zeolite and release the silver, the radioactivity removing with the slag. The silver containing metallic impurities is remelted and treated with oxygen and a flux to remove the metal impurities. About 98% of the silver in the silver exchanged zeolite having a purity of 99% or better is recoverable by the method.

  11. Intercalation of Layered Silicates, Layered Double Hydroxides, and Lead Iodide: Synthesis, Characterization and Properties.

    NASA Astrophysics Data System (ADS)

    Mehrotra, Vivek

    Layered silicates, layered double hydroxides, and lead iodide are lamellar solids that can incorporate guest species into the galleries between their layers. Various intercalated forms of these layered materials have been synthesized and their properties studied. The dielectric behavior of pristine fluorohectorite, a typical layered silicate, and Zn-Al layered double hydroxide is explained by considering the structural ordering and mobility of the intercalated water molecules, as well as models invoking fractal time processes and fractal structure. Intercalative polymerization of aniline and pyrrole into fluorohectorite leads to a multilayered structure consisting of single polymer chains alternately stacked with the 9.6 A thick silicate layers. The polymer chains are confined to the quasi two-dimensional interlayer space between the rigid host layers. The hybrid films exhibit highly anisotropic properties. The optical, electrical and mechanical behavior is discussed in terms of the molecular confinement of the polymer chains. Ethylenediamine functionalized C _{60} clusters have also been intercalated into fluorohectorite via an ion-exchange procedure. Intercalation results in an improved thermal stability of the functionalized C_{60} clusters. Rutherford backscattering spectrometry has been used to elucidate the mechanism of intercalative ion exchange of silver in muscovite mica, a layered silicate with a layer charge density of 2e per unit cell. It is proposed that ion-exchange progresses by intercalating successive galleries through the edges of the mica layers. Guest-host interactions have been studied in the system aniline-PbI_2. The optical and structural effects of aniline intercalation in lead iodide thin films is discussed. Intercalation leads to a large shift in the optical band gap of PbI_2. The observed change in band gap is not only due to the increased separation between the PbI_2 layers but also because of an electrostatic interaction between the

  12. Iodide iontophoresis as a treatment for dry eye syndrome

    PubMed Central

    Horwath-Winter, J; Schmut, O; Haller-Schober, E-M; Gruber, A; Rieger, G

    2005-01-01

    Background/aims: Among the causes related to the development or perpetuation and aggravation of dry eye disease, oxidative reactions may have a role in the pathogenesis of this disorder. Antioxidants, such as iodide, have shown a strong effect in preventing the oxidative damage to constituents of the anterior part of the eye. In this clinical trial the effectiveness of iodide iontophoresis and iodide application without current in moderate to severe dry eye patients was compared. Methods: 16 patients were treated with iodide iontophoresis and 12 patients with iodide application without current for 10 days. Subjective improvement, frequency of artificial tear application, tear function parameters (break up time, Schirmer test without local anaesthesia), vital staining (fluorescein and rose bengal staining) as well as impression cytology of the bulbar conjunctiva were evaluated before treatment, 1 week, 1 month, and 3 months after treatment. Results: A reduction in subjective symptoms, frequency of artificial tear substitute application, and an improvement in certain tear film and ocular surface factors could be observed in both groups. A stronger positive influence was seen after application of iodide with current (iontophoresis), as observed in a distinct improvement in break up time, fluorescein and rose bengal staining, and in a longer duration of this effect compared with the non-current group. No significant change in Schirmer test results and impression cytology were observed in both groups. Conclusions: Iodide iontophoresis has been demonstrated to be a safe and well tolerated method of improving subjective and objective dry eye factors in patients with ocular surface disease. PMID:15615744

  13. Silver(II) Oxide or Silver(I,III) Oxide?

    ERIC Educational Resources Information Center

    Tudela, David

    2008-01-01

    The often called silver peroxide and silver(II) oxide, AgO or Ag[subscript 2]O[subscript 2], is actually a mixed oxidation state silver(I,III) oxide. A thermochemical cycle, with lattice energies calculated within the "volume-based" thermodynamic approach, explain why the silver(I,III) oxide is more stable than the hypothetical silver(II) oxide.…

  14. Mineral commodity profiles: Silver

    USGS Publications Warehouse

    Butterman, W.C.; Hilliard, Henry E.

    2005-01-01

    Overview -- Silver is one of the eight precious, or noble, metals; the others are gold and the six platinum-group metals (PGM). World mine production in 2001 was 18,700 metric tons (t) and came from mines in 60 countries; the 10 leading producing countries accounted for 86 percent of the total. The largest producer was Mexico, followed by Peru, Australia, and the United States. About 25 percent of the silver mined in the world in 2001 came from silver ores; 15 percent, from gold ores and the remaining 60 percent, from copper, lead, and zinc ores. In the United States, 14 percent of the silver mined in 2001 came from silver ores; 39 percent, from gold ores; 10 percent, from copper and copper-molybdenum ores; and 37 percent, from lead, zinc, and lead-zinc ores. The precious metal ores (gold and silver) came from 30 lode mines and 10 placer mines; the base-metal ores (copper, lead, molybdenum, and zinc) came from 24 lode mines. Placer mines yielded less than 1 percent of the national silver production. Silver was mined in 12 States, of which Nevada was by far the largest producer; it accounted for nearly one-third of the national total. The production of silver at domestic mines generated employment for about 1,100 mine and mill workers. The value of mined domestic silver was estimated to be $290 million. Of the nearly 27,000 t of world silver that was fabricated in 2001, about one-third went into jewelry and silverware, one-fourth into the light-sensitive compounds used in photography, and nearly all the remainder went for industrial uses, of which there were 7 substantial uses and many other small-volume uses. By comparison, 85 percent of the silver used in the United States went to photography and industrial uses, 8 percent to jewelry and silverware, and 7 percent to coins and medals. The United States was the largest consumer of silver followed by India, Japan, and Italy; the 13 largest consuming countries accounted for nearly 90 percent of the world total. In the

  15. Synthesis, structural characterization and microbial activity of 2D Ag(I)-5-aminoisophthalate coordination polymer with a new coordination mode

    NASA Astrophysics Data System (ADS)

    Günay, Handan; Çolak, Alper Tolga; Yeşilel, Okan Zafer; Tunç, Tuncay; Çolak, Ferdağ

    2015-11-01

    In this study, a novel polynuclear Ag(I)-5-aminoisophthalate complex [Ag(μ4-Haip)]n (1) (H2aip = 5-aminoisophthalic acid) has been synthesized. The molecular structure of this complex has been determined by the single crystal X-ray diffraction. The two-dimensional polynuclear complex is crystallized in the triclinic crystal system with space group P-1. The Ag(I) ion is four-coordinated by three carboxylate oxygen atoms of three different Haip ligands and one nitrogen atom in a distorted tetrahedral geometry. Furthermore, a novel coordination mode has shown by H2aip. This complex exhibits photoluminescence in the solid state at room temperature. Antimicrobial activity of complex was evaluated by the agar diffusion method. The complex showed antimicrobial activity against tested microorganism strains (Gram positive, gram negative bacteria, clinic isolate yeast and mold). Moreover this complex showed particularly high antifungal activity against yeast and mold.

  16. Selective recovery of Ag(I) coordination anion from simulate nickel electrolyte using corn stalk based adsorbent modified by ammonia-thiosemicarbazide.

    PubMed

    Xiong, Ying; Wan, Li; Xuan, Jing; Wang, Yongwei; Xing, Zhiqing; Shan, Weijun; Lou, Zhenning

    2016-01-15

    In nickel electrolyte, Ag(I) was present at trace level concentration (10-20 mg L(-1)) and existed in the form of AgCli(1-i) coordination anion, instead of Ag(+) positive ion usually in several sources. In the present study, TSC-NH3-OCS adsorbent based on natural corn stalk modified by ammonia (NH3)-thiosemicarbazide (TSC) was synthesized and characterized using some instrumental techniques. The TSC-NH3-OCS adsorbent could selectively adsorb Ag(I) as AgCl(i)(1-i) coordination anion from the Ag(I)-Cu(II)-Ni(II) simulate nickel electrolyte, especially in the case of the very high levels of Cu(II) and Ni(II), which significantly outperforms the commercial available resins. The adsorption mechanism was believed to be electrostatic interaction of the protonated bands of AgCl4(3-) with protonated thiol form of the thioamide units by FTIR and XPS analysis. The maximum adsorption capacity in the Ag(I) single and Ag(I)-Cu(II)-Ni(II) ternary system were obtained and calculated as 153.54 and 46.69 mg g(-1), respectively. The reasons that the maximum adsorption capacity of AgCl(i)(1-i) from the single and ternary system varied widely could be explained by adsorption kinetic and thermodynamic results. In addition, three successive sorption/desorption cycle runs from ternary system were performed which indicated that the TSC-NH3-OCS adsorbent has a good performance for recovery Ag(I) from simulate nickel electrolyte. PMID:26368801

  17. Silver(I)-Catalyzed Addition of Phenols to Alkyne Cobalt Cluster Stabilized Carbocations.

    PubMed

    Valderas, Carolina; Casarrubios, Luis; Lledos, Agusti; Ortuño, Manuel A; de la Torre, María C; Sierra, Miguel A

    2016-06-20

    A smooth catalytic method to use phenols as the nucleophilic partner in the Nicholas reaction has been developed. The method uses either Ag(I) or Au(I) catalysts with AgClO4 or AgBF4 as the most efficient catalysts tested. Neither additional additives nor cocatalysts were required and the formation of the corresponding phenol adducts occurred in excellent yields. The process has the single limitation of the inability of less nucleophilic phenols (4-nitrophenol) to generate the corresponding adducts. Additionally, the reaction is highly diastereoselective. DFT calculations allow a catalytic cycle to be proposed that involves trimetallic intermediates; the rate-determining step of the reaction is hydroxy-group elimination in a cobalt-silver trimetallic intermediate. PMID:27187529

  18. NMR and specific heat study of atomic dynamics and spin-orbit behavior in Cu2-xAgyTe

    NASA Astrophysics Data System (ADS)

    Sirusi, Ali A.; Ballikaya, Sedat; Chen, Jing-Han; Uher, Ctirad; Ross, Joseph H., Jr.

    We report studies of Cu2Te and Cu2-xAgyTe, promising candidates for thermoelectric and photovoltaic applications. Cu and Te NMR show that above a well-defined 200 K onset, Cu2Te exhibits Cu-ion hopping, leading to the higher-temperature superionic motion. In Cu1.98Ag0.2Te the onset increases to 250 K. In the low-temperature static phase the properties are nearly identical. Aside from Korringa terms there are large diamagnetic contributions for all nuclei, comparable to those for other systems with very large spin-orbit and/or inverted band configurations. Thus the system may be a topologically interesting system like the similar phase Ag2Te. Results will be compared to DFT calculations of NMR shifts. The low-temperature spectra also indicate two distinct local environments for Cu sites, one corresponding to high symmetry such as characterizes the high-temperature cubic phase, and one with much more asymmetry. In addition, specific heat results are consistent with about 50% of the Cu ions being weakly bound on Einstein-oscillator sites. We tentatively connect these results to reported local inhomogeneity due to vacancy condensation in similar systems.

  19. Redox-Robust Pentamethylferrocene Polymers and Supramolecular Polymers, and Controlled Self-Assembly of Pentamethylferricenium Polymer-Embedded Ag, AgI, and Au Nanoparticles.

    PubMed

    Gu, Haibin; Ciganda, Roberto; Castel, Patricia; Vax, Amélie; Gregurec, Danijela; Irigoyen, Joseba; Moya, Sergio; Salmon, Lionel; Zhao, Pengxiang; Ruiz, Jaime; Hernández, Ricardo; Astruc, Didier

    2015-12-01

    We report the first pentamethylferrocene (PMF) polymers and the redox chemistry of their robust polycationic pentamethylferricenium (PMFium) analogues. The PMF polymers were synthesized by ring-opening metathesis polymerization (ROMP) of a PMF-containing norbornene derivative by using the third-generation Grubbs ruthenium metathesis catalyst. Cyclic voltammetry studies allowed us to determine confidently the number of monomer units in the polymers through the Bard-Anson method. Stoichiometric oxidation by using ferricenium hexafluorophosphate quantitatively and instantaneously provided fully stable (even in aerobic solutions) blue d(5) Fe(III) metallopolymers. Alternatively, oxidation of the PMF-containing polymers was conducted by reactions with Ag(I) or Au(III) , to give PMFium polymer-embedded Ag and Au nanoparticles (NPs). In the presence of I2 , oxidation by using Ag(I) gave polymer-embedded Ag/AgI NPs and AgNPs at the surface of AgI NPs. Oxidation by using Au(III) also produced an Au(I) intermediate that was trapped and characterized. Engineered single-electron transfer reactions of these redox-robust nanomaterial precursors appear to be a new way to control their formation, size, and environment in a supramolecular way. PMID:26494439

  20. Efficient removal of radioactive iodide ions from water by three-dimensional Ag2O-Ag/TiO2 composites under visible light irradiation.

    PubMed

    Liu, Shuaishuai; Wang, Na; Zhang, Yuchang; Li, Yaru; Han, Zhuo; Na, Ping

    2015-03-01

    Three-dimensional Ag2O and Ag co-loaded TiO2 (3D Ag2O-Ag/TiO2) composites have been synthesized through a facile method, characterized using SEM, EDX, TEM, XRD, XPS, UV-vis DRS, BET techniques, and applied to remove radioactive iodide ions (I(-)). The photocatalytic adsorption capacity (207.6 mg/g) of the 3D Ag2O-Ag/TiO2 spheres under visible light is four times higher than that in the dark, which is barely affected by other ions, even in simulated salt lake water where the concentration of Cl(-) is up to 590 times that of I(-). The capability of the composites to remove even trace amounts of I(-) from different types of water, e.g., deionized or salt lake water, is demonstrated. The composites also feature good reusability, as they were separated after photocatalytic adsorption and still performed well after a simple regeneration. Furthermore, a mechanism explaining the highly efficient removal of radioactive I(-) has been proposed according to characterization analyses of the composites after adsorption and subsequently been verified by adsorption and desorption experiments. The proposed cooperative effects mechanism considers the interplay of three different phenomena, namely, the adsorption performance of Ag2O for I(-), the photocatalytic ability of Ag/TiO2 for oxidation of I(-), and the readsorption performance of AgI for I2. PMID:25463231

  1. Bismuth tri-iodide radiation detector development

    NASA Astrophysics Data System (ADS)

    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

  2. Modified purification of mercuric iodide for crystal growth

    NASA Astrophysics Data System (ADS)

    Skinner, N. L.; Ortale, C.; Schieber, M. M.; Vandenberg, L.

    The standard procedure used in our laboratory to purify commercially available mercuric iodide consists of a sequence of steps: (1) repeated sublimation under continous evacuation, followed by (2) melting and recrystallization, and (3) a sublimation process in a closed tube. This paper describes a modification of the standard purification sequence by adding recrystallization of the mercuric iodide in hydrochloric acid. Leaching cation impurities out of mercuric iodide powder with hydrochloric acid has been practiced before by Zaletin, (V.M. Zaletin, I.H. Nozhiua, I.N. Fomin, V.T. Shystov, and N.V. Protasov, Atomic Energy 48, 169 (1980)). Our objective for the hydrochloric acid treatment was to remove nitrates and hydrocarbons which were interfering with the vapor transport during crystal growth. Results of the procedure are presented in terms of total carbon and selected ion content of the treated and untreated material.

  3. The BaBar cesium iodide electromagnetic calorimeter

    SciTech Connect

    Wuest, C.R.

    1994-12-01

    The BABAR Cesium Iodide Electromagnetic Calorimeter is currently in the technical design stage. The calorimeter consists of approximately 10,000 individual thallium-doped cesium iodide crystals arranged in a near-hermetic barrel and endcap structure. Taking previous cesium iodide calorimeters as a benchmark, we hope to build a system with roughly two times better energy resolution. This will be achieved by a combination of high quality crystal growing, precision mechanical processing of crystals and support structure, highly efficient light collection and low noise readout electronics. The calorimeter described here represents the current state of the design and we are undertaking an active period of optimization before this design is finalized. We discuss here the physics motivation, the current design and options for optimization.

  4. Thyroid effects of iodine and iodide in potable water

    NASA Technical Reports Server (NTRS)

    Bull, Richard J.; Thrall, Karla D.; Sherer, Todd T.

    1991-01-01

    Experiments are reviewed which examine the comparative toxicological effects of iodide (I) and iodine (I2) when used to disinfect drinking water. References are made to a subchronic study in rats, a comparison of the distribution of radiolabeled I and I2, and a demonstration of thyroxine formation in the gastrointestinal tract. The results of the study of the rats are examined in detail; the findings show that I and I2 have opposite effects on the concentrations of thyroid hormones in blood. Iodide slightly decreases circulating thyroxine, while I2 significantly increases the thyroxine concentrations, decreases triiodothyronine levels, and does not change the weight of the thyroid gland. The related effects of I2 ingestion are set forth in detail and are shown to be unique to I2 contamination. Iodine can counteract the effects of iodide and should therefore be used as a disinfectant in drinking water.

  5. Phase 1 Methyl Iodide Deep-Bed Adsorption Tests

    SciTech Connect

    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

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

    PubMed

    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

  7. Label-free detection of native proteins by surface-enhanced Raman spectroscopy using iodide-modified nanoparticles.

    PubMed

    Xu, Li-Jia; Zong, Cheng; Zheng, Xiao-Shan; Hu, Pei; Feng, Jia-Min; Ren, Bin

    2014-02-18

    Proteins perform vital functional and structural duties in living systems, and the in-depth investigation of protein in its native state is one of the most important challenges in the postgenomic era. Surface-enhanced Raman spectroscopy (SERS) can provide the intrinsic fingerprint information of samples with ultrahigh sensitivity but suffers from the reproducibility and reliability issues. In this paper, we proposed an iodide-modified Ag nanoparticles method (Ag IMNPs) for label-free detection of proteins. The silver nanoparticles provide the huge enhancement to boost the Raman signal of proteins, and the coated iodide layer offers a barrier to prevent the direct interaction between the proteins and the metal surface, helping to keep the native structures of proteins. With this method, highly reproducible and high-quality SERS signals of five typical proteins (lysozyme, avidin, bovine serum albumin, cytochrome c, and hemoglobin) have been obtained, and the SERS features of the proteins without chromophore were almost identical to the respective normal Raman spectra. This unique feature allows the qualitative identification of them by simply taking the intensity ratio of the Raman peaks of tryptophan to phenylalanine residues. We further demonstrated that the method can also be used for label-free multiplex analysis of protein mixture as well as to study the dynamic process of protein damage stimulated by hydrogen peroxide. This method proves to be very promising for further applications in proteomics and biomedical research. PMID:24460183

  8. Silver recovery system data

    SciTech Connect

    Boulineau, B.

    1991-08-26

    In August of 1990 the Savannah River Site Photography Group began testing on a different type of silver recovery system. This paper describes the baseline study and the different phases of installation and testing of the system.

  9. Mercuric Iodide Anticoincidence Shield for Gamma-Ray Spectrometer

    NASA Technical Reports Server (NTRS)

    Hartsough, Neal; Iwanczyk, Jan

    2009-01-01

    A film-growth process was developed for polycrystalline mercuric iodide that creates cost-effective, large-area detectors for high-energy charged-particle detection. A material, called a barrier film, is introduced onto the substrate before the normal mercuric iodide film growth process. The barrier film improves the quality of the normal film grown and enhances the adhesion between the film and the substrate. The films grown using this improved technique were found to have adequate signal-to-noise properties so that individual high-energy charged -particle interactions could be distinguished from noise, and thus, could be used to provide an anticoincidence veto function as desired.

  10. Chiral one- and two-dimensional silver(I)-biotin coordination polymers.

    PubMed

    Altaf, Muhammad; Stoeckli-Evans, Helen

    2013-02-01

    Reaction of biotin {C(10)H(16)N(2)O(3)S, HL; systematic name: 5-[(3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanoic acid} with silver acetate and a few drops of aqueous ammonia leads to the deprotonation of the carboxylic acid group and the formation of a neutral chiral two-dimensional polymer network, poly[[{μ(3)-5-[(3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanoato}silver(I)] trihydrate], {[Ag(C(10)H(15)N(2)O(3)S)]·3H(2)O}(n) or {[Ag(L)]·3H(2)O}(n), (I). Here, the Ag(I) cations are pentacoordinate, coordinated by four biotin anions via two S atoms and a ureido O atom, and by two carboxylate O atoms of the same molecule. The reaction of biotin with silver salts of potentially coordinating anions, viz. nitrate and perchlorate, leads to the formation of the chiral one-dimensional coordination polymers catena-poly[[bis[nitratosilver(I)]-bis{μ(3)-5-[(3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanoato}] monohydrate], {[Ag(2)(NO(3))(2)(C(10)H(16)N(2)O(3)S)(2)]·H(2)O}(n) or {[Ag(2)(NO(3))(2)(HL)(2)]·H(2)O}(n), (II), and catena-poly[bis[perchloratosilver(I)]-bis{μ(3)-5-[(3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanoato}], [Ag(2)(ClO(4))(2)(C(10)H(16)N(2)O(3)S)(2)](n) or [Ag(2)(ClO(4))(2)(HL)(2)](n), (III), respectively. In (II), the Ag(I) cations are again pentacoordinated by three biotin molecules via two S atoms and a ureido O atom, and by two O atoms of a nitrate anion. In (I), (II) and (III), the Ag(I) cations are bridged by an S atom and are coordinated by the ureido O atom and the O atoms of the anions. The reaction of biotin with silver salts of noncoordinating anions, viz. hexafluoridophosphate (PF(6)(-)) and hexafluoridoantimonate (SbF(6)(-)), gave the chiral double-stranded helical structures catena-poly[[silver(I)-bis{μ(2)-5-[(3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanoato}] hexafluoridophosphate], {[Ag(C(10)H(16)N(2)O(3)S)(2)](PF(6))}(n) or {[Ag(HL)(2)](PF(6

  11. Electrical studies on silver based fast ion conducting glassy materials

    NASA Astrophysics Data System (ADS)

    Rao, B. Appa; Kumar, E. Ramesh; Kumari, K. Rajani; Bhikshamaiah, G.

    2014-04-01

    Among all the available fast ion conductors, silver based glasses exhibit high conductivity. Further, glasses containing silver iodide enhances fast ion conducting behavior at room temperature. Glasses of various compositions of silver based fast ion conductors in the AgI-Ag2O-[(1-x)B2O3-xTeO2] (x=0 to1 mol% in steps of 0.2) glassy system have been prepared by melt quenching method. The glassy nature of the compounds has been confirmed by X-ray diffraction. The electrical conductivity (AC) measurements have been carried out in the frequency range of 1 KHz-3MHz by Impedance Analyzer in the temperature range 303-423K. The DC conductivity measurements were also carried out in the temperature range 300-523K. From both AC and DC conductivity studies, it is found that the conductivity increases and activation energy decreases with increasing the concentration of TeO2 as well as with temperature. The conductivity of the present glass system is found to be of the order of 10-2 S/cm at room temperature. The ionic transport number of these glasses is found to be 0.999 indicating that these glasses can be used as electrolyte in batteries.

  12. Electrical studies on silver based fast ion conducting glassy materials

    SciTech Connect

    Rao, B. Appa Kumar, E. Ramesh Kumari, K. Rajani Bhikshamaiah, G.

    2014-04-24

    Among all the available fast ion conductors, silver based glasses exhibit high conductivity. Further, glasses containing silver iodide enhances fast ion conducting behavior at room temperature. Glasses of various compositions of silver based fast ion conductors in the AgI−Ag{sub 2}O−[(1−x)B{sub 2}O{sub 3}−xTeO{sub 2}] (x=0 to1 mol% in steps of 0.2) glassy system have been prepared by melt quenching method. The glassy nature of the compounds has been confirmed by X-ray diffraction. The electrical conductivity (AC) measurements have been carried out in the frequency range of 1 KHz–3MHz by Impedance Analyzer in the temperature range 303–423K. The DC conductivity measurements were also carried out in the temperature range 300–523K. From both AC and DC conductivity studies, it is found that the conductivity increases and activation energy decreases with increasing the concentration of TeO{sub 2} as well as with temperature. The conductivity of the present glass system is found to be of the order of 10{sup −2} S/cm at room temperature. The ionic transport number of these glasses is found to be 0.999 indicating that these glasses can be used as electrolyte in batteries.

  13. γ-Selective Allylation of (E)-Alkenylzinc Iodides Prepared by Reductive Coupling of Arylacetylenes with Alkyl Iodides.

    PubMed

    Zhurkin, Fedor E; Hu, Xile

    2016-07-01

    The first examples of Cu-catalyzed γ-selective allylic alkenylation using organozinc reagents are reported. (E)-Alkenylzinc iodides were prepared by Fe-catalyzed reductive coupling of terminal arylalkynes with alkyl iodides. In the presence of a copper catalyst, these reagents reacted with allylic bromides derived from Morita-Baylis-Hillman alcohols to give 1,4-dienes in high yields. The reactions are highly γ-selective (generally γ/α > 49:1) and tolerate a wide range of functional groups such as ester, cyano, keto, and nitro. PMID:27285459

  14. PolyA-tailed and fluorophore-labeled aptamer-gold nanoparticle conjugate for fluorescence turn-on bioassay using iodide-induced ligand displacement.

    PubMed

    Li, Wei; Dong, Yifan; Wang, Xi; Li, Hui; Xu, Danke

    2015-04-15

    Depending on the strong affinity of polyA sequence to gold (or silver) surface, applicability of polyA-tailed DNA-gold (or silver) nanoparticle conjugates in homogeneous and heterogeneous protein assays was first demonstrated. Interestingly, when using polyA-tailed, fluophore-labeled DNA-AuNP conjugate, it was found that iodide and thiosulfate anions could act as the ligand displacing reagent to detach polyA-tailed DNA strands from AuNP surface and simultaneously activate the AuNP-quenched fluorophores by destroying the polyA-AuNP interaction via a divide-and-conquer strategy. Based on this new discovery, we have developed a novel, cost-effective and sandwich-type fluorescence turn-on aptasensor for highly sensitive and specific thrombin detection, what took advantage of aptamer-conjugated magnetic beads (apt-MBs) for protein capture and separation, and iodide-induced fluorescence recovery of activatable polyA-based AuNP probes through ligand displacement for fluorescence turn-on detection. This proposed aptasensor could detect thrombin specifically with a detection limit as low as 89pM, which was better than or comparable to many existing fluorescent thrombin assays. Importantly, employment of such polyA-based AuNP conjugate not only avoids the use of thiolated oligonucleotides and thiol-containing displacing reagents, but also offers new possibilities for fabricating convenient and cost-effective bioanalytical applications. PMID:25460880

  15. 40 CFR 415.510 - Applicability; description of the potassium iodide production subcategory.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... potassium iodide production subcategory. 415.510 Section 415.510 Protection of Environment ENVIRONMENTAL... SOURCE CATEGORY Potassium Iodide Production Subcategory § 415.510 Applicability; description of the potassium iodide production subcategory. The provisions of this subpart are applicable to...

  16. 40 CFR 415.510 - Applicability; description of the potassium iodide production subcategory.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... potassium iodide production subcategory. 415.510 Section 415.510 Protection of Environment ENVIRONMENTAL... SOURCE CATEGORY Potassium Iodide Production Subcategory § 415.510 Applicability; description of the potassium iodide production subcategory. The provisions of this subpart are applicable to...

  17. 40 CFR 415.510 - Applicability; description of the potassium iodide production subcategory.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... potassium iodide production subcategory. 415.510 Section 415.510 Protection of Environment ENVIRONMENTAL... SOURCE CATEGORY Potassium Iodide Production Subcategory § 415.510 Applicability; description of the potassium iodide production subcategory. The provisions of this subpart are applicable to...

  18. 40 CFR 415.510 - Applicability; description of the potassium iodide production subcategory.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... potassium iodide production subcategory. 415.510 Section 415.510 Protection of Environment ENVIRONMENTAL... SOURCE CATEGORY Potassium Iodide Production Subcategory § 415.510 Applicability; description of the potassium iodide production subcategory. The provisions of this subpart are applicable to...

  19. 40 CFR 415.510 - Applicability; description of the potassium iodide production subcategory.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... potassium iodide production subcategory. 415.510 Section 415.510 Protection of Environment ENVIRONMENTAL... SOURCE CATEGORY Potassium Iodide Production Subcategory § 415.510 Applicability; description of the potassium iodide production subcategory. The provisions of this subpart are applicable to...

  20. Development of a mercuric iodide solid state spectrometer for X-ray astronomy

    NASA Technical Reports Server (NTRS)

    Vallerga, J.

    1983-01-01

    Mercuric iodide detectors, experimental development for astronomical use, X ray observations of the 1980 Cygnus X-1 High State, astronomical had X ray detectors in current use, detector development, balloon flight of large area (1500 sq cm) Phoswich detectors, had X ray telescope design, shielded mercuric iodide background measurement, Monte Carlo analysis, measurements with a shielded mercuric iodide detector are discussed.

  1. Degradation of Methyl Iodide in Soil: Effects of Environmental Factors

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Methyl iodide (MeI) is a promising alternative to the phased-out fumigant methyl bromide, and its environmental fate following soil fumigation is of great concern. Experiments were conducted to investigate the effect of various environmental factors on the degradation rate of MeI in soil. The chem...

  2. Physical property measurements of doped cesium iodide crystals

    NASA Technical Reports Server (NTRS)

    Synder, R. S.; Clotfelter, W. N.

    1974-01-01

    Mechanical and thermal property values are reported for crystalline cesium iodide doped with sodium and thallium. Young's modulus, bulk modulus, shear modulus, and Poisson's ratio were obtained from ultrasonic measurements. Young's modulus and the samples' elastic and plastic behavior were also measured under tension and compression. Thermal expansion and thermal conductivity were the temperature dependent measurements that were made.

  3. DEGRADATION OF METHYL IODIDE IN SOIL: EFFECTS OF ENVIRONMENTAL FACTORS

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Methyl iodide (MeI) is a promising alternative to the phased-out fumigant methyl bromide; however, there are concerns about its environmental fate following soil fumigation. Laboratory experiments were conducted to investigate the effect of various environmental factors on the degradation rate of ...

  4. Coordination polymers of Ag(I) based on iminocarbene ligands involving metal-carbon and metal-heteroatom interactions

    NASA Astrophysics Data System (ADS)

    Netalkar, Sandeep P.; Netalkar, Priya P.; Revankar, Vidyanand K.

    2016-03-01

    The reaction of Ag2O with three novel imino-NHC ligands derived from 2-chloroacetophenone with pendant N-donor functional group incorporated by reaction with methoxyamine and 1-methyl/ethyl/n-butyl-substituted imidazoles afforded one-dimensional coordination polymers with [(-NHCarbene)Ag(NHCarbene-)PF6]n formulation involving both carbon-metal and heteroatom-metal interactions, the carbon and heteroatom involved in coordination to silver being from different molecule of the ligand. The complexes as well as the ligands were characterized by spectroscopic methods as well as the solid state structures determined in case of 2a, 3a and complex 5. The iminocarbene ligands serve as non-chelating building block for supramolecular silver assemblies.

  5. Leaching of Silver from Silver-Impregnated Food Storage Containers

    ERIC Educational Resources Information Center

    Hauri, James F.; Niece, Brian K.

    2011-01-01

    The use of silver in commercial products has proliferated in recent years owing to its antibacterial properties. Food containers impregnated with micro-sized silver promise long food life, but there is some concern because silver can leach out of the plastic and into the stored food. This laboratory experiment gives students the opportunity to…

  6. The effect of 1:2 Ag(I) thiocyanate complexes in MCF-7 breast cancer cells.

    PubMed

    Ferreira, Eloise; Munyaneza, Appollinaire; Omondi, Bernard; Meijboom, Reinout; Cronjé, Marianne J

    2015-08-01

    There is much interest currently in the design of metal compounds as drugs and various metal compounds are already in clinical use. These include gold(I) compounds such as auranofin and the anti-cancer platinum(II) complex, cisplatin. Bis-chelated gold(I) phosphine complexes have also shown great potential as anticancer agents, however, their efficacy has been limited by their high toxicity. In this study, silver(I) thiocyanate compounds linked to four specific ligands, were synthesized and characterized. These silver-phosphine adducts included [AgSCN{P(4-MeC6H4)3}2]2 (1); [AgSCN{P(4-ClC6H4)3}2]2 (2); [AgSCN{P(4-MeOC6H4)3}2]2 (3); [AgSCN(PPh3)2]2 (4). The compounds were found to be toxic to MCF-7 breast cancer cells while the ligands on their own were not toxic. Our findings further indicate that the silver(I) phosphine compounds induce apoptotic cell death in these breast cancer cells. In addition, the compounds were not toxic to nonmalignant fibroblast cells at the IC50 concentrations. This is an indication that the compounds show selectivity towards the cancer cells. PMID:26049979

  7. Direct vapor/solid synthesis of mercuric iodide using compounds of mercury and iodine

    DOEpatents

    Skinner, Nathan L.

    1990-01-01

    A process is disclosed for producing high purity mercuric iodide by passing a gaseous source of a mercuric compound through a particulate bed of a low vapor pressure iodide compound which is maintained at an elevated temperature which is the lower of either: (a) just below the melting or volatilization temperature of the iodide compound (which ever is lower); or (b) just below the volatilization point of the other reaction product formed during the reaction; to cause the mercuric compound to react with the iodide compound to form mercuric iodide which then passes as a vapor out of the bed into a cooler condensation region.

  8. Synthesis of (/sup 75/Se)trimethylselenonium iodide from (/sup 75/Se)selenocystine

    SciTech Connect

    Foster, S.J.; Ganther, H.E.

    1984-02-15

    The synthesis of (/sup 75/Se)trimethylselenonium iodide from (/sup 75/)selenocystine is described. The starting compound is reduced to (/sup 75/Se)selenocysteine with borohydride and reacted with methyl iodide to form (/sup 75/Se)Se-methyl-selenocysteine, then treated with methyl iodide in formic acid solution to form Se-dimethyl-selenocysteine selenonium iodide. Over a period of days, the selenonium intermediate undergoes spontaneous elimination to form alanine and dimethyl selenide, which reacts with methyl iodide to give the trimethylselenonium product in over 90% yield. 15 references.

  9. Determination of ultra-trace amounts of silver in water by differential pulse anodic stripping voltammetry using a new modified carbon paste electrode.

    PubMed

    El-Mai, Hafida; Espada-Bellido, Estrella; Stitou, Mostafa; García-Vargas, Manuel; Galindo-Riaño, Maria Dolores

    2016-05-01

    A highly sensitive and selective new procedure for the determination of silver in aqueous media was developed using a modified carbon paste electrode (MCPE) by differential pulse anodic stripping voltammetry (DPASV). The modified electrode was based on the incorporation of 2-hydroxybenzaldehyde benzoylhydrazone (2-HBBH) in the carbon paste electrode. Silver ions were preconcentrated on the modified electrode at open-circuit by complexation with the ligand and reduced to zero valent at a potential of 0V, and followed by the reoxidation of adsorbed ions onto the electrode by scanning the potential in a positive direction. The oxidation peak of Ag(I) was observed at 0.2V (versus Ag/AgCl). The analysis of Ag(I) was carried out in a cell containing the sample solution (20mL) buffered by 0.1molL(-1) K2HPO4/NaOH at pH 5.5 in aqueous solution and nitric acid (pH 1) in real water samples. The optimum conditions for the analysis of silver include a reduction potential of 0V and a pulse amplitude of 100mV, among others. The optimum carbon paste composition was found to be 14.1% (w/w) 2-HBBH, 56.2% (w/w) graphite powder and 29.7% (w/w) paraffin oil. Differential pulse anodic stripping voltammetric response was used as the analytical signal. Under the selected conditions, the voltammetric signal was proportional to the Ag(I) concentration in the range of 0.001-100μgL(-1) with favorable limits of detection and quantification of 1.1ngL(-1) and 3.7ngL(-1) after 3min of accumulation time, respectively. By increasing the accumulation time to 10min, detection and quantification limits can be further improved up to 0.1ngL(-1) and 0.34ngL(-1), respectively. In addition, the results showed a highly reproducible procedure showing a relative standard deviation of 1.5% for 12 replicate measurements. Many coexisting metal ions were investigated and very few interferences were found on the determination of Ag(I). The proposed method was validated using certified reference estuarine waters

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

    PubMed

    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

  11. Silver-iron batteries

    NASA Astrophysics Data System (ADS)

    Lindstroem, O.

    1980-04-01

    Production methods for iron electrodes were studied. It was found that a sintering temperature of 700 C gave the best strength and capacity. Production methods and additions for silver electrodes were also studied. The capacity of the produced iron and silver electrodes were 1100 mAh/cu cm. Different separators were investigated. Cellophane I and II from Du Pont was found to be the best. In tests open cells achieved 60 percent of the calculated capacity. In order to minimize the increase of the pressure in closed cells different additions to the electrodes were studied.

  12. Mercuric iodide (HgI2) growth for nuclear detectors

    NASA Technical Reports Server (NTRS)

    Schnepple, W.

    1982-01-01

    The purpose of this investigation is to grow more-perfect mercuric iodide crystals in a low-gravity environment by taking advantage of diffusion-controlled growth conditions and by avoiding the problem of strain dislocations produced by the crystal's weight. This crystal has considerable practical importance as a sensitive gamma-ray detector and energy spectrometer that can operate at ambient temperature, as compared to presently available detectors that must be cooled to near liquid nitrogen temperatures. However, the performance of mercuric iodide crystals only rarely approaches the expected performance, presumably because some of the free electrical charges produced within the crystal are not collected at the electrodes, but instead remain trapped or immobilized at crystal defects. An efficient high atomic number semiconductor detector capable of operating at room temperature utilizing single HgI2 crystals offers a greater potential than existing detector technology.

  13. Purification and deposition of silicon by an iodide disproportionation reaction

    DOEpatents

    Wang, Tihu; Ciszek, Theodore F.

    2002-01-01

    Method and apparatus for producing purified bulk silicon from highly impure metallurgical-grade silicon source material at atmospheric pressure. Method involves: (1) initially reacting iodine and metallurgical-grade silicon to create silicon tetraiodide and impurity iodide byproducts in a cold-wall reactor chamber; (2) isolating silicon tetraiodide from the impurity iodide byproducts and purifying it by distillation in a distillation chamber; and (3) transferring the purified silicon tetraiodide back to the cold-wall reactor chamber, reacting it with additional iodine and metallurgical-grade silicon to produce silicon diiodide and depositing the silicon diiodide onto a substrate within the cold-wall reactor chamber. The two chambers are at atmospheric pressure and the system is open to allow the introduction of additional source material and to remove and replace finished substrates.

  14. Iodide and albumin kinetics in normal canine wrists and knees

    SciTech Connect

    Simkin, P.A.; Benedict, R.S. )

    1990-01-01

    The clearance rates of free iodide and of radioiodinated serum albumin were measured in the knee and wrist joints of 9 normal adult dogs. Iodide clearance from the knee was 3 times greater than that from the wrist. In contrast, radioiodinated serum albumin clearance from the knee was only slightly greater than that from the wrist. Interpreted as respective indices of effective synovial plasma flow and lymphatic drainage, these values indicate that the filtration fraction is normally greater in microvessels of the wrist than in those of the knee. These findings complement the results of companion studies of Starling forces that indicate a higher pressure microvascular bed in the wrist than in the knee.

  15. A silver complex with tryptophan: Synthesis, structural characterization, DFT studies and antibacterial and antitumor assays in vitro

    NASA Astrophysics Data System (ADS)

    Carvalho, Marcos A.; de Paiva, Raphael E. F.; Bergamini, Fernando R. G.; Gomes, Alexandre F.; Gozzo, Fábio C.; Lustri, Wilton R.; Formiga, André L. B.; Shishido, Silvia M.; Ferreira, Carmen V.; Corbi, Pedro P.

    2013-01-01

    The synthesis, spectroscopic characterization and biological assays of a new silver(I) complex with L-tryptophan (TRP) are presented. Elemental and thermal analyses and ESI-QTOF mass spectrometric measurements of the solid compound suggest the composition AgC11H11N2O2. Infrared and solid-state NMR analyses indicate coordination of TRP to Ag(I) ion through the nitrogen of the NH2 group and also through the oxygen of carboxylate group. Theoretical (DFT) calculations permit proposing an optimized geometry for the complex. Antibacterial assays indicated that the Ag-TRP complex is effective against Staphylococcus aureus and Enterococcus faecalis (Gram-positive), and Pseudomonas aeruginosa and Escherichia coli (Gram-negative) bacterial strains. The complex was also cytotoxic against Panc-1 (human pancreatic carcinoma) and SK-Mel 103 (human melanoma) cells.

  16. Tales From Silver Lands.

    ERIC Educational Resources Information Center

    Finger, Charles J.

    In 1925, "Tales From Silver Lands" was awarded the Newbery medal as the most distinguished contribution to American children's literature for the year. The book contains a collection of 19 short stories learned from the Indians of South America as the author traveled to different lands. As described on the dust jacket, the tales are about "strange…

  17. Potassium silver cyanide

    Integrated Risk Information System (IRIS)

    Jump to main content . Integrated Risk Information System Recent Additions | Contact Us Search : All EPA IRIS • You are here : EPA Home • Research • Environmental Assessment • IRIS • IRIS Summaries Redirect Page As of September 28 , 2010 , the assessment summary for potassium silver cyanide is inclu

  18. Antibacterial activity and toxicity of silver - nanosilver versus ionic silver

    NASA Astrophysics Data System (ADS)

    Kvitek, L.; Panacek, A.; Prucek, R.; Soukupova, J.; Vanickova, M.; Kolar, M.; Zboril, R.

    2011-07-01

    The in vitro study of antibacterial activity of silver nanoparticles (NPs), prepared via modified Tollens process, revealed high antibacterial activity even at very low concentrations around several units of mg/L. These concentrations are comparable with concentrations of ionic silver revealing same antibacterial effect. However, such low concentrations of silver NPs did not show acute cytotoxicity to mammalian cells - this occurs at concentrations higher than 60 mg/L of silver, while the cytotoxic level of ionic silver is much more lower (approx. 1 mg/L). Moreover, the silver NPs exhibit lower acute ecotoxicity against the eukaryotic organisms such as Paramecium caudatum, Monoraphidium sp. and D. melanogaster. The silver NPs are toxic to these organisms at the concentrations higher than 30 mg/L of silver. On contrary, ionic silver retains its cytoxicity and ecotoxicity even at the concentration equal to 1 mg/L. The performed experiments demonstrate significantly lower toxicity of silver NPs against the eukaryotic organisms than against the prokaryotic organisms.

  19. Infrared attenuation of thallium bromo-iodide fibers

    NASA Technical Reports Server (NTRS)

    Magilavy, B.; Goebel, J.

    1986-01-01

    Analysis of attenuation measurements in the near infrared of an unclad fiber of Thallium Bromo-Iodide (Th(Br,I)), a polycrystalline thallium halide, is presented. A general overview is given of the properties of fiber optics. Two groups of attenuation measurements, for the region 1.2 to 3.4 and for 3 to 11 microns, respectively, are presented, analyzed, and compared with those of two other groups of researchers.

  20. Growth of mercuric iodide single crystals from dimethylsulfoxide

    DOEpatents

    Carlston, Richard C.

    1976-07-13

    Dimethylsulfoxide is used as a solvent for the growth of red mercuric iodide (HgI.sub.2) crystals for use in radiation detectors. The hygroscopic property of the solvent allows controlled amounts of water to enter into the solvent phase and diminish the large solubility of HgI.sub.2 so that the precipitating solid collects as well-defined euhedral crystals which grow into a volume of several cc.

  1. Self-pairing of 1-methylthymine mediated by two and three Ag(i) ions: a gas phase study using infrared dissociation spectroscopy and density functional theory.

    PubMed

    Nosenko, Yevgeniy; Riehn, Christoph; Niedner-Schatteburg, Gereon

    2016-03-16

    Metal base pairs of Ag(I) cations and 1-methylthymine (1MT) or deprotonated 1-methylthymine (1MT-H) are produced and analyzed by electrospray ionization mass spectrometry (ESI-MS). Mass-selected ions of type [Ag2(1MT)(1MT-H)](+) and [Ag3(1MT-H)2](+) are interrogated by infrared multiple-photon dissociation (IRMPD) in an ion trap in the range of 1200-3700 cm(-1). Supporting spectroscopic data were obtained from the investigation of the analogous 2'-deoxy-thymidine complexes which exhibit advantageously high fragment yields. By comparison with calculated linear IR spectra (obtained by density functional theory, DFT) we assign the structures and the possible isomeric forms of these metal base pairs and their dependence on the number of mediating Ag(I) ions. Based on the observed Ag(+)/1MT complexes and related polarizable continuum model DFT calculations we describe the probable formation pathways in aqueous solution. The present findings pave the way for subsequent UV investigations of the multi-metal mediated base pairs. PMID:26940234

  2. Mitigating iodomethane emissions and iodide residues in fumigated soils.

    PubMed

    Xuan, Richeng; Ashworth, Daniel J; Wu, Laosheng; Yates, Scott R

    2013-11-19

    Although long-regarded as an excellent soil fumigant for killing plant pests, methyl bromide (MeBr) was phased out in 2005 in the USA, because it can deplete the stratospheric ozone layer. Iodomethane (MeI) has been identified as an effective alternative to MeBr and is used in a number of countries for preplant pest control. However, MeI is highly volatile and potentially carcinogenic to humans if inhaled. In addition, iodide anions, a breakdown product of MeI, can build up in fumigated soils and potentially cause plant toxicity and contaminate groundwater via leaching. In order to overcome the above two obstacles in MeI application, a method is proposed to place reactive bags containing ammonium hydroxide solution (NH4OH) on the soil surface underneath an impermeable plastic film covering the fumigated area. Our research showed that using this approach, over 99% of the applied MeI was quantitatively transferred to iodide. Of all the resulting iodide, only 2.7% remained in the fumigated soil, and 97.3% was contained in the reactive bag that can be easily removed after fumigation. PMID:24151978

  3. Characterization of Electrochemically Generated Silver

    NASA Technical Reports Server (NTRS)

    Adam, Niklas; Martinez, James; Carrier, Chris

    2014-01-01

    Silver biocide offers a potential advantage over iodine, the current state of the art in US spacecraft disinfection technology, in that silver can be safely consumed by the crew. Low concentrations of silver (<500 ppb) have been shown to kill bacteria in water systems and keep it safe for potability. Silver does not require hardware to remove it from a water system, and therefore can provide a simpler means for disinfecting water. The Russian segment of the International Space Station has utilized an electrochemically generated silver solution, which is colloidal in nature. To be able to reliably provide a silver biocide to drinking water by electrochemical means would reduce mass required for removing another biocide such as iodine from the water. This would also aid in crew time required to replace iodine removal cartridges. Future long term missions would benefit from electrochemically produced silver as the biocide could be produced on demand and requires only a small concentration to be effective. Since it can also be consumed safely, there is less mass in removal hardware and little consumables required for production. The goal of this project initially is to understand the nature of the electrochemically produced silver, the particle sizes produced by the electrochemical cell and the effect that voltage adjustment has on the particle size. In literature, it has been documented that dissolved oxygen and pH have an effect on the ionization of the electrochemical silver so those parameters would be measured and possibly adjusted to understand their effect on the silver.

  4. Iodide interactions with clay minerals: Batch and diffusion studies

    NASA Astrophysics Data System (ADS)

    Miller, A. W.; Kruichak, J.; Mills, M.; Wang, Y.

    2012-12-01

    Clay minerals are likely candidates to aid in nuclear waste isolation due to their low permeability, favorable swelling properties, and high cation sorption capacities. Iodine-129 is often the major driver of exposure risk from nuclear waste repositories at timescales >10,000 years. Therefore, understanding the geochemical cycling of iodine in clays is critical in developing defensible quantitative descriptions of nuclear waste disposal. Anions are not typically considered to interact with most clays as it is assumed that the fixed negative charge of clays actively repels the dissoloved anion. This is corroborated by many batch studies, but diffusion experiments in compacted clays have shown iodide retardation relative to chloride. The reasons for this are unknown; however, several possible hypotheses include: redox transformation controls on sorption behavior, complex surface charge environments due to overlapping charge domains, and sorption to ancillary minerals or weathering products. Seven different clay minerals have been examined using several techniques to chracterize the surface charge environment and iodide uptake. The use of a series of clays shifts the independent variable away from water chemistry characteristics (pH, contaminant concentration), and toward structural characterisitics of clay minerals including isomorphous substitution and clay texture. Iodide uptake batch experiments were completed with the clay minerals in a range of swamping electrolytes. The results give evidence for a novel uptake mechanism involving ion pair formation and iodide concentration within nano-confined environments. These results were further tested using diffusional columns where nano-confined regimes make up a larger proportion of the total porosity. These columns were compacted to different hydrostatic pressures and saturated with different ionic compositions. Porosity distributions were characterized with a fluoride tracer. Iodide diffusion characteristics were

  5. Templated Synthesis of Silver(I) and Copper(II) Nanostructures: Solid State Reactions and Applications

    NASA Astrophysics Data System (ADS)

    Bourret, Gilles R.

    2011-12-01

    This Thesis presents the synthesis of novel 1D, 2D, and 3D Ag(I) and Cu(II) nanostructures and their use as sacrificial templates to make functional nanomaterials. New soft template methods were developed for the synthesis of AgCN and Cu(OH)2 nanostructures. Polymeric organic nanotubes were successfully used to synthesize AgCN nanowires, while the precipitation of Cu(OH)2 nanofibers was templated in water microdroplets. Both methods benefit from the versatility of soft templates and allows for a control of both the size and the morphology of the nanostructures produced. The conversion of these precursors into metallic and semi-conductive nanomaterials was achieved via chemical and electrochemical reduction, and thermolysis. Chemical reduction of the AgCN nanowires leads to the fabrication of conductive arrays on nylon filter substrates, while the thermolysis of the Cu(OH)2 spherical assemblies yields photoresponsive semi-conductive porous CuO spheres. The electrochemical reduction of the native Ag(I) and Cu(II) one-dimensional nanostructures was investigated in aqueous solution at gold/glass/gold junctions. The solid-solid conversion involved in the electrochemical reduction process was studied via cyclic voltammetry, chronoamperometry, and electronic microscopy. The strong influence of the reduction potential on the nanomaterials produced allowed for the fabrication of a range of Ag(0) nanostructures, including nanoparticles, nanoprisms, nanofibers and porous networks. Electrochemical reduction of Au/M2+/Au junctions leads to the formation of an excellent electrical contact between the two gold electrodes. This technique was expanded to include ionically-conductive Ag2S nanowires which form metallic/ionic-conductor heterojunctions. Keywords: nanostructure, nanowire, template, emulsion, electrochemistry, silver, cyanide, copper, oxide, heterojunction, sacrificial template.

  6. Silver oxide nanocrystals anchored on titanate nanotubes and nanofibers: promising candidates for entrapment of radioactive iodine anions

    NASA Astrophysics Data System (ADS)

    Yang, Dongjiang; Liu, Hongwei; Liu, Long; Sarina, Sarina; Zheng, Zhanfeng; Zhu, Huaiyong

    2013-10-01

    Iodine radioisotopes are released into the environment by the nuclear industry and medical research institutions using radioactive materials. The 129I- anion is one of the more mobile radioactive species due to a long half-life, and it is a great challenge to design long-term management solutions for such radioactive waste. In this study, a new adsorbent structure with the potential to efficiently remove radioactive iodine anions (I-) from water is devised: silver oxide (Ag2O) nanocrystals firmly anchored on the surface of titanate nanotubes and nanofibers via coherent interfaces between Ag2O and titanate phases. I- anions in fluids can easily access the Ag2O nanocrystals and be efficiently trapped by forming AgI precipitate that firmly attaches to the adsorbent. Due to their one-dimensional morphology, the new adsorbents can be readily dispersed in liquids and easily separated after purification; and the adsorption beds loaded with the adsorbents can permit high flux. This significantly enhances the adsorption efficiency and reduces the separation costs. The proposed structure reveals a new direction in developing efficient adsorbents for the removal of radioactive anions from wastewater.Iodine radioisotopes are released into the environment by the nuclear industry and medical research institutions using radioactive materials. The 129I- anion is one of the more mobile radioactive species due to a long half-life, and it is a great challenge to design long-term management solutions for such radioactive waste. In this study, a new adsorbent structure with the potential to efficiently remove radioactive iodine anions (I-) from water is devised: silver oxide (Ag2O) nanocrystals firmly anchored on the surface of titanate nanotubes and nanofibers via coherent interfaces between Ag2O and titanate phases. I- anions in fluids can easily access the Ag2O nanocrystals and be efficiently trapped by forming AgI precipitate that firmly attaches to the adsorbent. Due to their one

  7. Hydrometallurgical recovery of silver from waste silver oxide button cells

    NASA Astrophysics Data System (ADS)

    Sathaiyan, N.; Nandakumar, V.; Ramachandran, P.

    In recent years, recycling of household batteries has attracted much attention mainly with respect to environmental aspects in addition to the savings. Small silver oxide primary cells used in electric watches become a waste after their life is over. Recycling procedures are needed to prevent any environmental impact from these wastes and to recover the value inherent in the scrap. Smelting and electrolytic methods are discussed for silver recovery from this battery waste. Acid leaching of waste batteries and precipitation of silver as silver chloride followed by smelting at 1000 °C yields a silver recovery of about 83%. An electrolytic route is studied as an alternative to the smelting operation and involves the electrodeposition of silver with higher purity from a silver thiosulfate complex prepared from silver chloride. The electrolysis is potentiostatically controlled at a potential of -0.400 to -0.600 V (SCE) for avoiding side-reactions such as the sulfiding of silver. Although recovery methods have been identified in principle, their suitability for mixed small battery waste and economic factors have yet to be demonstrated.

  8. Extraction of Silver by Glucose.

    PubMed

    Baksi, Ananya; Gandi, Mounika; Chaudhari, Swathi; Bag, Soumabha; Gupta, Soujit Sen; Pradeep, Thalappil

    2016-06-27

    Unprecedented silver ion leaching, in the range of 0.7 ppm was seen when metallic silver was heated in water at 70 °C in presence of simple carbohydrates, such as glucose, making it a green method of silver extraction. Extraction was facilitated by the presence of anions, such as carbonate and phosphate. Studies confirm a two-step mechanism of silver release, first forming silver ions at the metal surface and later complexation of ionic silver with glucose; such complexes have been detected by mass spectrometry. Extraction leads to microscopic roughening of the surface making it Raman active with an enhancement factor of 5×10(8) . PMID:27119514

  9. Genetics Home Reference: Russell-Silver syndrome

    MedlinePlus

    ... Genetics Home Health Conditions Russell-Silver syndrome Russell-Silver syndrome Enable Javascript to view the expand/collapse ... Download PDF Open All Close All Description Russell-Silver syndrome is a growth disorder characterized by slow ...

  10. New simultaneous catalytic determination of thiocyanate and iodide by flow injection analysis

    SciTech Connect

    Tanaka, A.; Miyazaki, M.; Deguchi, T.

    1985-01-01

    Flow injection analysis (FIA) with a double injection technique was applied to catalytic determination of thiocyanate and iodide in the redox reaction between cerium(IV) and arsenic(III). Selective inactivation of the catalytic activity of thiocyanate was investigated. Amounts of only iodide and amounts of both thiocyanate and iodide were simultaneously determined by the FIA. Detection limits of the method were 0.2 ppM SCN/sup -/ and 0.1 ppM I/sup -/.

  11. Silver Ink For Jet Printing

    NASA Technical Reports Server (NTRS)

    Vest, R. W.; Singaram, Saraswathi

    1989-01-01

    Metallo-organic ink containing silver (with some bismuth as adhesion agent) applied to printed-circuit boards and pyrolized in air to form electrically conductive patterns. Ink contains no particles of silver, does not have to be mixed during use to maintain homogeneity, and applied to boards by ink-jet printing heads. Consists of silver neodecanoate and bismuth 2-ethylhexanoate dissolved in xylene and/or toluene.

  12. Silver Nanoparticles in Dental Biomaterials

    PubMed Central

    Corrêa, Juliana Mattos; Mori, Matsuyoshi; Sanches, Heloísa Lajas; da Cruz, Adriana Dibo; Poiate, Isis Andréa Venturini Pola

    2015-01-01

    Silver has been used in medicine for centuries because of its antimicrobial properties. More recently, silver nanoparticles have been synthesized and incorporated into several biomaterials, since their small size provides great antimicrobial effect, at low filler level. Hence, these nanoparticles have been applied in dentistry, in order to prevent or reduce biofilm formation over dental materials surfaces. This review aims to discuss the current progress in this field, highlighting aspects regarding silver nanoparticles incorporation, such as antimicrobial potential, mechanical properties, cytotoxicity, and long-term effectiveness. We also emphasize the need for more studies to determine the optimal concentration of silver nanoparticle and its release over time. PMID:25667594

  13. MOD silver metallization for photovoltaics

    NASA Technical Reports Server (NTRS)

    Vest, G. M.; Vest, R. W.

    1984-01-01

    The development of flat plate solar arrays is reported. Photovoltaic cells require back side metallization and a collector grid system on the front surface. Metallo-organic decomposition (MOD) silver films can eliminate most of the present problems with silver conductors. The objectives are to: (1) identify and characterize suitable MO compounds; (2) develop generic synthesis procedures for the MO compounds; (3) develop generic fabrication procedures to screen printable MOD silver inks; (4) optimize processing conditions to produce grid patterns and photovoltaic cells; and (5) develop a model which describes the adhesion between the fired silver film and the silicon surface.

  14. IUPAC-NIST Solubility Data Series. 94. Rare Earth Metal Iodides and Bromides in Water and Aqueous Systems. Part 1. Iodides

    NASA Astrophysics Data System (ADS)

    Mioduski, Tomasz; Gumiński, Cezary; Zeng, Dewen

    2012-03-01

    This work presents solubility data for rare earth metal iodides in water and in aqueous ternary systems. Compilations of all available experimental data are introduced for each rare earth metal iodide with a corresponding critical evaluation. Every such evaluation contains a tabulated collection of all solubility results in water, a selection of suggested solubility data and a brief discussion of the multicomponent systems. Because the ternary systems were almost never studied more than once, no critical evaluations of such data were possible. Only simple iodides (no complexes) are treated as the input substances in this work. The literature has been covered through the middle of 2011.

  15. Specific adsorption of halide and pseudohalide ions at electrochemically roughened versus smooth silver-aqueous interfaces

    NASA Astrophysics Data System (ADS)

    Hupp, Joseph T.; Larkin, D.; Weaver, Michael J.

    1983-02-01

    The differential capacitance of electrochemically roughened silver surfaces in mixed perchlorate electrolytes containing chloride, bromide, iodide, thiocyanate, or azide anions has been measured as a function of electrode potential and anion concentration. These results are compared with corresponding data for electropolished silver in order to ascertain the influence of surface roughening on the double-layer structure and composition of polycrystalline silver-aqueous interfaces. The surface concentrations of specifically adsorbed anions were obtained from these capacitance-potential data using a "Hurwitz-Parsons" type of analysis. Although electrochemical roughening by means of a conventional oxidation-reduction cycle in chloride media is a prerequisite to the appearance of Surface-Enhanced Raman Scattering (SERS) for these adsorbates, it yields only moderate (ca. 1.5- to 2-fold) increases in the actual surface area and has a relatively minor effect on their average surface concentration. However, roughening does induce noticeable changes in the morphology of the capacitance-potential curves which are traced to alterations in the surface-crystallite structure. Comparisons between the potential dependence of SERS with corresponding capacitance-potential data indicate that anion coverages close to a monolayer are necessary for stable SERS. This is attributed to the stabilization of Raman-active silver clusters by surrounding adsorbed anions.

  16. Carbon aging mechanisms and effects on retention of organic iodides

    SciTech Connect

    Hyder, M.L.

    1985-01-01

    The activated carbon used to treat the off-gas from the Savannah River Plant prodution reactor building was studied to determine the chemical changes occurring in this carbon during its service life. The carbon is a coconut-shell charcoal impregnated with 1% triethylenediamine (TEDA) and 2% KI. It was known that during its 30-month service life the carbon becomes more acidic and less effective for retaining iodine in organic form. The study showed that the most important change occurring in the carbon is the reaction of KI to give other chemical forms of iodine. The reacted iodine is unavailable for exchange with alkyl iodides. The results suggest that the carbon reacts with KI to form organic compounds, but small amounts of oxidized iodine may also be presnt. There is also evidence that some iodide is lost from the carbon altogether. The TEDA impregnant is lost from the carbon very quickly, and has no importance after a few months. The specific reactions by which the impregnant is lost have not been identified. However, mathematical analysis shows that the carbon performance data are consistent with the reaction of iodide impregnant with impurities in the air flowing through the carbon bed. Additional mathematical analysis, based on electron microscopic observation of the carbon particles, indicates that the external surfaces of the carbon are mainly responsible for their effectiveness in retaining iodine. Consequently, the condition of the impregnants on a relatively small fraction of the carbon surface can have a large effect on its performance. 4 refs., 14 figs., 2 tabs.

  17. Mechanical testing of large thallium doped sodium iodide single crystals

    NASA Technical Reports Server (NTRS)

    Lee, H. M.

    1985-01-01

    The findings of mechanical tests performed on five thallium-doped sodium iodide NaI(Tl) crystals are presented. These crystals are all in the shape of circular flat plates, 20.0 in. in diameter an d0.5 in. thick. The test setup, testing procedure, and the test data are presented. Large crystals exhibit a high degree of material plasticity, as well as a much higher strength than previously anticipated, on the order of 500 psi. Also revealed from the testing is the fact that crystal with a large number of grain boundaries developed less plasticity, and therefore less permanent deformation, than those with fewer grain boundaries.

  18. Copper Mediated Difluoromethylation of Aryl and Vinyl Iodides

    PubMed Central

    Fier, Patrick S.

    2012-01-01

    Selectively fluorinated molecules are important as materials, pharmaceuticals, and agrochemicals, but their synthesis by simple, mild, laboratory methods is challenging. We report a straightforward method for the cross-coupling of a difluoromethyl group with readily available reagents to form difluoromethylarenes. The reaction of electron-neutral, electron-rich, and sterically hindered aryl and vinyl iodides with the combination of CuI, CsF and TMSCF2H leads to the formation of difluoromethylarenes in high yield with good functional group compatibility. This transformation is surprising, in part, because of the prior observation of the instability of CuCF2H. PMID:22397683

  19. Au25(SG)18 as a fluorescent iodide sensor

    NASA Astrophysics Data System (ADS)

    Wang, Man; Wu, Zhikun; Yang, Jiao; Wang, Guozhong; Wang, Hongzhi; Cai, Weiping

    2012-06-01

    The recently emerging gold nanoclusters (GNC) are of major importance for both basic science studies and practical applications. Based on its surface-induced fluorescence properties, we investigated the potential use of Au25(SG)18 (GSH: glutathione) as a fluorescent iodide sensor. The current detection limit of 400 nM, which can possibly be further enhanced by optimizing the conditions, and excellent selectivity among 12 types of anion (F-, Cl-, Br-, I-, NO3-, ClO4-, HCO3-, IO3-, SO42-, SO32-, CH3COO- and C6H5O73-) make Au25(SG)18 a good candidate for iodide sensing. Furthermore, our work has revealed the particular sensing mechanism, which was found to be affinity-induced ratiometric and enhanced fluorescence (abbreviated to AIREF), which has rarely been reported previously and may provide an alternative strategy for devising nanoparticle-based sensors.The recently emerging gold nanoclusters (GNC) are of major importance for both basic science studies and practical applications. Based on its surface-induced fluorescence properties, we investigated the potential use of Au25(SG)18 (GSH: glutathione) as a fluorescent iodide sensor. The current detection limit of 400 nM, which can possibly be further enhanced by optimizing the conditions, and excellent selectivity among 12 types of anion (F-, Cl-, Br-, I-, NO3-, ClO4-, HCO3-, IO3-, SO42-, SO32-, CH3COO- and C6H5O73-) make Au25(SG)18 a good candidate for iodide sensing. Furthermore, our work has revealed the particular sensing mechanism, which was found to be affinity-induced ratiometric and enhanced fluorescence (abbreviated to AIREF), which has rarely been reported previously and may provide an alternative strategy for devising nanoparticle-based sensors. Electronic supplementary information (ESI) available: fluorescence spectra of Au25(SG)18 (1.6 μM in H2O) with successive titration of I- and the time-dependent fluorescence of Au25(SG)18. See DOI: 10.1039/c2nr30169e.

  20. Rutherford backscattering and Auger spectroscopy of mercuric iodide detectors

    NASA Astrophysics Data System (ADS)

    Felter, T. E.; Stulen, R. H.; Schnepple, W. F.; Ortale, C.; van den Berg, L.

    1989-11-01

    Palladium contacts on mercuric iodide have been studied using Rutherford backscattering spectroscopy and Auger electron spectroscopy. Results on actual detector contacts show some intermixing of both mercury and iodine with the palladium. To investigate the role of processing variables as a possible cause of this effect we have fabricated model contacts at low temperatures (T ≈ 100 K) and analyzed in situ. The results demonstrated that significant interdiffusion occurs at temperatures as low as 225 K. We conclude that excessive heating during contact deposition could prove to be detrimental to device performance and that the use of cooled substrates during processing should be explored.

  1. Low-temperature photoluminescence studies of mercuric-iodide photodetectors

    NASA Astrophysics Data System (ADS)

    James, R. B.; Bao, X. J.; Schlesinger, T. E.; Markakis, J. M.; Cheng, A. Y.; Ortale, C.

    1989-09-01

    Mercuric-iodide (HgI2 ) photodetectors with sputtered indium-tin-oxide (ITO) entrance electrodes were studied using low-temperature photoluminescence spectroscopy. The photoluminescence spectrum obtained on each photodetector was found to differ for points beneath the ITO contact and points adjacent to it, indicating that the contact fabrication process introduces new carrier traps and radiative recombination centers within the ITO-HgI2 interfacial region. In particular, a new broad band was observed in the spectra taken from points beneath the ITO electrode. Photocurrent-versus-position measurements showed that the intensity of this broad band was enhanced in regions having relatively poor photoresponse.

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

    PubMed

    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

  3. Development of mercuric iodide uncooled x ray detectors and spectrometers

    NASA Technical Reports Server (NTRS)

    Iwanczyk, Jan S.

    1990-01-01

    The results obtained in the development of miniature, lowpower, light weight mercuric iodide, HgI2, x ray spectrometers for future space missions are summarized. It was demonstrated that HgI2 detectors can be employed in a high resolution x ray spectrometer, operating in a scanning electron microscope. Also, the development of HgI2 x ray detectors to augment alpha backscattering spectrometers is discussed. These combination instruments allow for the identification of all chemical elements, with the possible exception of hydrogen, and their respective concentrations. Additionally, further investigations of questions regarding radiation damage effects in the HgI2 x ray detectors are reported.

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

    NASA Astrophysics Data System (ADS)

    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.

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

    PubMed

    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

  6. Optical transmission measurements on monocrystalline and polycrystalline cesium iodide

    NASA Technical Reports Server (NTRS)

    Viehmann, W.; Arens, J. F.; Simon, M.

    1973-01-01

    A summary is presented of optical measurements performed on a variety of cesium iodide samples to characterize quantitatively the optical quality of the materials, and to define and measure parameters which determine its suitability as a detector material for high energy cosmic ray experiments on HEAO-A. The general case of light transmission through a long rectangular slab under multiple internal reflections is discussed along with transmission and scattering as a function of wavelength at normal incidence. Scattering parameters are tabulated for encapsulated single crystal CsI and polyscin.

  7. Temperature dependent energy levels of methylammonium lead iodide perovskite

    SciTech Connect

    Foley, Benjamin J.; Marlowe, Daniel L.; Choi, Joshua J. E-mail: mgupta@virginia.edu; Sun, Keye; Gupta, Mool C. E-mail: mgupta@virginia.edu; Saidi, Wissam A.; Scudiero, Louis E-mail: mgupta@virginia.edu

    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.

  8. Highly sensitive and selective colorimetric sensing of Hg2+ based on the morphology transition of silver nanoprisms.

    PubMed

    Chen, Ling; Fu, Xiuli; Lu, Wenhui; Chen, Lingxin

    2013-01-23

    A simple colorimetric approach for mercury ion (Hg(2+)) sensing was developed that was based on the Hg(2+)-induced deprotection and morphology transition of 1-dodecanethiol (C(12)H(25)SH)-capped silver nanoprisms (Ag NPRs) upon the presence of iodides at room temperature. The abstraction of C(12)H(25)SH from the surface of Ag NPRs by Hg(2+) led to their deprotection of Ag NPRs and the formation of complexation between silver ions and excess iodide ions. Also, the silver atoms were consumed and moved from the surface of Ag NPRs, accompanying the changes in the particle morphology that resulted in a change of color and UV-vis absorption spectra of the colloidal solution. With increasing concentrations of Hg(2+) from 10 to 500 nM, the surface plasma resonance spectral band of Ag NPRs emerged as a blue shift and exhibited a good linear relationship, and the limit of detection was 3.3 nM. Furthermore, the developed method was applied for detecting Hg(2+) in different real water samples with satisfying recoveries over 92%. PMID:23237272

  9. An Ag(I) energetic metal-organic framework assembled with the energetic combination of furazan and tetrazole: synthesis, structure and energetic performance.

    PubMed

    Qu, Xiao-Ni; Zhang, Sheng; Wang, Bo-Zhou; Yang, Qi; Han, Jing; Wei, Qing; Xie, Gang; Chen, San-Ping

    2016-04-28

    A novel Ag(I) energetic MOF [Ag16(BTFOF)9]n·[2(NH4)]n () assembled with Ag(iI ions and a furazan derivative, 4,4'-oxybis[3,3'-(1H-5-tetrazol)]furazan (H2BTFOF) was successfully synthesized and structurally characterized, featuring a three-dimensional porous structure incorporating ammonium cations. The thermal stability and energetic properties were determined, revealing that the 3D energetic MOF had an outstanding insensitivity (IS > 40 J), an ultrahigh detonation pressure (P) of 65.29 GPa and a detonation velocity (D) of 11.81 km cm(-3). In addition, the self-accelerating decomposition temperature (TSADT) and the critical temperature of thermal explosion (Tb) are also discussed in detail. The finding exemplifies that the assembly strategy plays a decisive role in the density and energetic properties of MOF-based energetic materials. PMID:26987079

  10. Relationship of dietary iodide and drinking water disinfectants to thyroid function in experimental animals

    SciTech Connect

    Revis, N.W.; McCauley, P.; Holdsworth, G.

    1986-11-01

    The importance of dietary iodide on the reported hypothyroid effect of drinking water disinfectants on thyroid function was investigated. Previous studies have also showed differences in the relative sensitivity of pigeons and rabbits to chlorinated water. Pigeons and rabbits were exposed for 3 months to diets containing high (950 ppb) or low (300 ppb) levels of iodide and to drinking water containing two levels of chlorine. Results showed that the high-iodide diet prevented the hypothyroid effect observed in pigeons given the low-iodide diet and chlorinated drinking water. Similar trends were observed in rabbits exposed to the same treatment; however, significant hypothyroid effects were not observed in this animal model. The factor associated with the observed effect of dietary iodide on the chlorine-induced change in thyroid function is unknown, as is the relative sensitivity of rabbits and pigeons to the effect of chlorine. Several factors may explain the importance of dietary iodide and the relative sensitivity of these species. For example, the iodine formed by the known reaction of chlorine with iodide could result in a decrease in the plasma level of iodide because of the relative absorption rates of iodide and iodine in the intestinal tract, and the various types and concentrations of chloroorganics (metabolites) formed in the diet following the exposure of various dietary constituents to chlorine could affect the thyroid function. The former factor was investigated in the present studies. Results do not confirm a consistent, significant reduction in the plasma level of iodide in rabbits and pigeons exposed to chlorinated water and the low-iodide diet. The latter factor is being investigated.

  11. Corrosion protection for silver reflectors

    DOEpatents

    Arendt, Paul N.; Scott, Marion L.

    1991-12-31

    A method of protecting silver reflectors from damage caused by contact with gaseous substances which are often present in the atmosphere and a silver reflector which is so protected. The inventive method comprises at least partially coating a reflector with a metal oxide such as aluminum oxide to a thickness of 15 .ANG. or less.

  12. Nanoindentation studies on silver nanoparticles

    NASA Astrophysics Data System (ADS)

    Saha, Dhriti Ranjan; Mandal, Amrita; Mitra, Sreemanta; Mada, Mykanth Reddy; Boughton, Philip; Bandyopadhyay, Sri; Chakravorty, Dipankar

    2013-06-01

    Nanodimensional metallic silver was grown by electrodeposion technique in a semi solid polymer matrix of polyacrylamide. The whole structure looks like dendronic. The average particle diameter of the as grown metallic silver is 13 nm. Nanoindentation study of these nanoparticles shows modulus and hardness value as 103.93 GPa and 3.12 GPa respectively.

  13. Preparation and ion conductivity of composite films AgI-ZnO

    NASA Astrophysics Data System (ADS)

    Fateev, Sergey S.; Tveryanovich, Yu S.; Tomaev, V. V.; Fokina, Svetlana V.

    2015-05-01

    It has been proven that with laser deposition silver iodide retains its chemical composition and structure. A film has been produced with the help of laser deposition, consisting of finely divided crystals of ZnO and AgI. Its structure has been reviewed using X-Ray phase analysis, and its electric conductivity has been reviewed using impedance measurement. Special attention has been given to the effect of phase interaction on ion transport.

  14. Assembly of three new POM-based Ag(I) coordination polymers with antibacterial and photocatalytic properties

    NASA Astrophysics Data System (ADS)

    Lu, Xin-Xin; Luo, Yu-Hui; Lu, Chen; Chen, Xin; Zhang, Hong

    2015-12-01

    Three new silver coordination polymers, namely, {Ag3(bpy)6[PW12O40]} (1), {Ag5(H2biim)2(Hbiim-NO2)2[PW12O40]} (2), {Ag7(pytz)4[PW12O40]} (3) (bpy=2,2‧-bipyridine, H2biim=2,2‧-biimidazole, pytz=4-(1H-tetrazol-5-yl)pyridine), have been synthesized under hydrothermal condition. Compound 1 shows a 3D supramolecular framework based on 0D moieties. Compound 2 exhibits an attractive 2D biologic screw axis. Compound 3 displays a 3D structure, which consists of Ag(I)···π interactions, π···π stacking and weak Ag···Ag interactions. It is noteworthy that nitration happens to compound 2 during the hydrothermal condition, which is quite rare. Through contrasting the antibacterial activities of gram negative and gram positive bacteria, we find compounds 1-3 have better antibacterial property in gram negative bacteria than gram positive bacteria. In addition, compounds 1-3 also exhibit efficiency of photocatalytic decomposition of organic dyes. Those compounds may be used as potential multifunctional materials in wastewater treatment, because they not only can kill bacteria but also degrade organic pollutants.

  15. Iodide-catalyzed ozonation of terpenes on aqueous surfaces

    NASA Astrophysics Data System (ADS)

    Enami, S.; Hayase, S.; Kawasaki, M.; Hoffmann, M. R.; Colussi, A. J.

    2011-12-01

    Biogenic terpenes are the dominant global source of volatile organic compounds (VOC) and secondary organic aerosols (SOA). Their atmospheric chemistry has therefore major direct and indirect impacts on global climate change. At the same time, it has become apparent that organic and inorganic iodine species of marine origin are ubiquitous in the troposphere. They are found over the open ocean (even in the absence of biogenic sources), the Antarctic coast, in rain, aerosols, ice, and snow, and participate in HOx/NOx cycles in the troposphere. Here we report that iodide catalyzes the ozonation of alpha-pinene on aqueous surfaces. Nebulizer-assisted online electrospray mass spectrometry of alpha-pinene solutions briefly exposed to gaseous ozone reveals that alpha-pinene, which is unreactive during 10 microsecond contact times, is converted into acids (e.g., pinonic acid) and previously unreported iodine-containing species in the presence of millimolar iodide. These newly found products were characterized by MS/MS in conjunction with isotope and kinetic studies, and may account for unidentified organoiodine species observed in recent field measurements.

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

    PubMed

    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

  17. A Facile Method for the Synthesis of Binary Tungsten Iodides.

    PubMed

    Ströbele, Markus; Castro, Cristina; Fink, Reinhold F; Meyer, H-Jürgen

    2016-04-01

    The preparation of tungsten iodides in large quantities is a challenge because these compounds are not accessible using an easy synthesis method. A new, remarkably efficient route is based on a halide exchange reaction between WCl6 and SiI4 . The reaction proceeds at moderate temperatures in a closed glass vessel. The new compounds W3 I12 (W3 I8 ⋅2 I2 ) and W3 I9 (W3 I8 ⋅1/2  I2 ) containing the novel [W3 I8 ] cluster are formed at 120 and 150 °C, and remain stable in air. W3 I12 is an excellent starting material for the synthesis of other metal-rich tungsten iodides. At increasing temperature these trinuclear clusters undergo self-reduction until an octahedral tungsten cluster is formed in W6 I12 . The synthesis, structure, and an analysis of the bonding of compounds containing this new trinuclear tungsten cluster are presented. PMID:26947934

  18. Strontium Iodide Instrument Development for Gamma Spectroscopy and Radioisotope Identification

    SciTech Connect

    Beck, P; Cherepy, Nerine; Payne, Stephen A.; Swanberg, E.; Nelson, K.; Thelin, P; Fisher, S E; Hunter, Steve; Wihl, B; Shah, Kanai; Hawrami, Rastgo; Burger, Arnold; Boatner, Lynn A; Momayezi, M; Stevens, K; Randles, M H; Solodovnikov, D

    2014-01-01

    Development of the Europium-doped Strontium Iodide scintillator, SrI2(Eu), has progressed significantly in recent years. SrI2(Eu) has excellent material properties for gamma ray spectroscopy: high light yield (>80,000 ph/MeV), excellent light yield proportionality, and high effective atomic number (Z=49) for high photoelectric cross-section. High quality 1.5 and 2 diameter boules are now available due to rapid advances in SrI2(Eu) crystal growth. In these large SrI2(Eu) crystals, optical self-absorption by Eu2+ degrades the energy resolution as measured by analog electronics, but we mitigate this effect through on-the-fly correction of the scintillation pulses by digital readout electronics. Using this digital correction technique we have demonstrated energy resolution of 2.9% FWHM at 662 keV for a 4 in3 SrI2(Eu) crystal, over 2.6 inches long. Based on this digital readout technology, we have developed a detector prototype with greatly improved radioisotope identification capability compared to Sodium Iodide, NaI(Tl). The higher resolution of SrI2(Eu) yields a factor of 2 to 5 improvement in radioisotope identification (RIID) error rate compared to NaI(Tl).

  19. Efficient Use and Recycling of the Micronutrient Iodide in Mammals

    PubMed Central

    Rokita, Steven E.; Adler, Jennifer M.; McTamney, Patrick M.; Watson, James A.

    2010-01-01

    Daily ingestion of iodide alone is not adequate to sustain production of the thyroid hormones, tri- and tetraiodothyronine. Proper maintenance of iodide in vivo also requires its active transport into the thyroid and its salvage from mono- and diiodotyrosine that are formed in excess during hormone biosynthesis. The enzyme iodotyrosine deiodinase responsible for this salvage is unusual in its ability to catalyze a reductive dehalogenation reaction dependent on a flavin cofactor, FMN. Initial characterization of this enzyme was limited by its membrane association, difficult purification and poor stability. The deiodinase became amenable to detailed analysis only after identification and heterologous expression of its gene. Site-directed mutagenesis recently demonstrated that cysteine residues are not necessary for enzymatic activity in contrast to precedence set by other reductive dehalogenases. Truncation of the N-terminal membrane anchor of the deiodinase has provided a soluble and stable source of enzyme sufficient for crystallographic studies. The structure of an enzyme•substrate co-crystal has become invaluable for understanding the origins of substrate selectivity and the mutations causing thyroid disease in humans. PMID:20167242

  20. Ionic transport in hybrid lead iodide perovskite solar cells

    PubMed Central

    Eames, Christopher; Frost, Jarvist M.; Barnes, Piers R. F.; 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 (CH3NH3PbI3) are derived from first principles, and are compared with kinetic data extracted from the current–voltage response of a perovskite-based solar cell. We identify the microscopic transport mechanisms, and find facile vacancy-assisted migration of iodide ions with an activation energy of 0.6 eV, in good agreement with the kinetic measurements. The results of this combined computational and experimental study suggest that hybrid halide perovskites are mixed ionic–electronic conductors, a finding that has major implications for solar cell device architectures. PMID:26105623

  1. Crystal growth and scintillation properties of strontium iodide scintillators

    SciTech Connect

    van Loef, Edgar; Wilson, Cody; Cherepy, Nerine; Payne, Steven; Choong, Woon-Seng; Moses, William W.; Shah, Kanai

    2009-06-01

    Single crystals of SrI{sub 2}:Eu and SrI{sub 2}:Ce/Na were grown from anhydrous iodides by the vertical Bridgman technique in evacuated silica ampoules. Growth rates were of the order of 5-30 mm/day. Radioluminescence spectra of SrI{sub 2}:Eu and SrI{sub 2}:Ce/Na exhibit a broad band due to Eu{sup 2+} and Ce{sup 3+} emission, respectively. The maximum in the luminescence spectrum of SrI{sub 2}:Eu is found at 435 nm. The spectrum of SrI{sub 2}:Ce/Na exhibits a doublet peaking at 404 and 435 nm attributed to Ce{sup 3+} emission, while additional impurity - or defected - related emission is present at approximately 525 nm. The strontium iodide scintillators show very high light yields of up to 120,000 photons/MeV, have energy resolutions down to 3% at 662 keV (Full Width Half Maximum) and exhibit excellent light yield proportionality with a standard deviation of less than 5% between 6 and 460 keV.

  2. Strontium iodide instrument development for gamma spectroscopy and radioisotope identification

    NASA Astrophysics Data System (ADS)

    Beck, P. R.; Cherepy, N. J.; Payne, S. A.; Swanberg, E. L.; Nelson, K. E.; Thelin, P. A.; Fisher, S. E.; Hunter, S.; Wihl, B. M.; Shah, K. S.; Hawrami, R.; Burger, A.; Boatner, L. A.; Momayezi, M.; Stevens, K. T.; Randles, M. H.; Solodovnikov, D.

    2014-09-01

    Development of the Europium-doped Strontium Iodide scintillator, SrI2(Eu2+), has progressed significantly in recent years. SrI2(Eu2+) has excellent material properties for gamma ray spectroscopy: high light yield (<80,000 ph/MeV), excellent light yield proportionality, and high effective atomic number (Z = 49) for high photoelectric cross-section. High quality 1.5" and 2" diameter boules are now available due to rapid advances in SrI2(Eu) crystal growth. In these large SrI2(Eu) crystals, optical self-absorption by Eu2+ degrades the energy resolution as measured by analog electronics, but we mitigate this effect through on-the-fly correction of the scintillation pulses by digital readout electronics. Using this digital correction technique we have demonstrated energy resolution of 2.9% FWHM at 662 keV for a 4 in3 SrI2(Eu) crystal, over 2.6 inches long. Based on this digital readout technology, we have developed a detector prototype with greatly improved radioisotope identification capability compared to Sodium Iodide, NaI(Tl). The higher resolution of SrI2(Eu) yields a factor of 2 to 5 improvement in radioisotope identification (RIID) error rate compared to NaI(Tl).

  3. 9-O-Ethyl­berberrubinium iodide monohydrate

    PubMed Central

    Grundt, Peter; Pernat, Jennifer; Krivogorsky, Bogdana; Halverson, Melanie A.; Berry, Steven M.

    2010-01-01

    In the title compound (systematic name: 9-eth­oxy-10-meth­oxy-5,6-dihydro-1,3-dioxolo[4,5-g]isoquinolino­[3,2-a]isoquin­olin-7-ium iodide monohydrate), 2C21H20NO4 +·2I−·H2O, two independent mol­ecules pack in the unit cell, where interactions between the molecules are stabilized by weak inter­molecular π–π stacking inter­actions [centroid–centroid distances in the range 3.571 (4) to 3.815 (4)Å]. Inter­molecular C—H⋯O inter­actions are also observed. The iodide anions are disordered with occupancy ratios of 0.94 (1):0.06 (1) and 0.91 (1):0.09 (1). The cationic molecule is planar in structure with a small torsion resulting from the dihydropyridine ring. PMID:21587567

  4. Oxygen-hydrogen fuel cell with an iodine-iodide cathode - A concept

    NASA Technical Reports Server (NTRS)

    Javet, P.

    1970-01-01

    Fuel cell uses a porous cathode through which is fed a solution of iodine in aqueous iodide solution, the anode is a hydrogen electrode. No activation polarization appears on the cathode because of the high exchange-current density of the iodine-iodide electrode.

  5. Dose-Response Analysis of Developmental Iodide Deficiency: Reductions in Thyroid Hormones and Impaired Hippocampal Synaptic Transmission

    EPA Science Inventory

    Iodide is an essential nutrient for thyroid hormone synthesis and severe iodide deficiency (ID) during early development is associated with neurological impairments. Several environmental contaminants can perturb the thyroid axis and this perturbation may be more acute under cond...

  6. Copper iodide staining and determination of proteins adsorbed to microtiter plates.

    PubMed

    Root, D D; Reisler, E

    1990-04-01

    Copper iodide staining and determination of proteins adsorbed to polystyrene microtiter plates are described. The minimum amount of copper iodide-stained protein detected in densitometric measurements is approximately 20 pg/mm2. Enzyme immunoassay readers may also be used for the determination of copper iodide-stained proteins, but are less sensitive than densitometers. The densitometric readings of copper iodide-stained proteins vary linearly with the amount of protein present as verified by enzymatic and radioactive probes. Staining is complete in 2-3 min and may be removed by a 30-min treatment with EDTA without loss of adsorbed protein or immunoreactivity. The exact amount of protein adsorbed to microtiter plate wells can be measured by using protein bound and stained on nitrocellulose as a calibration curve. Copper iodide staining is a rapid, convenient, and inexpensive alternative to radioactive measurements of similar parameters. PMID:1694063

  7. A comparison between the gastric and salivary concentration of iodide, pertechnetate, and bromide in man

    PubMed Central

    Harden, R. McG.; Alexander, W. D.; Shimmins, J.; Chisholm, D.

    1969-01-01

    The concentration of iodide (I−) and pertechnetate (TcO4−) and bromide (Br−) has been measured simultaneously in gastric juice and parotid saliva. The combined gastric and salivary clearance for iodide and pertechnetate is more than twice the clearance of these ions by the thyroid gland. The concentration of the ions was in the order I−>TcO4−>Br− in both gastric juice and saliva. Differences exist between the secretion of iodide, pertechnetate, and bromide. Bromide, in contrast to iodide and pertechnetate, was found to be more concentrated in gastric juice than in saliva. The ratio of the iodide to pertechnetate clearance was greater in gastric juice than in saliva. PMID:5358585

  8. Solvent-free synthesis of alkylbenzimidazolium iodides and their applications in dye-sensitized solar cells

    SciTech Connect

    Xia, Mei; Shi, Chengwu; Sun, Renjie; Liu, Zhaokun; Cai, Molang

    2010-10-15

    In this paper, the synthesis of 1-hexyl-3-methylbenzimidazolium iodide (HMBI) and 1-hexyl-3-propylbenzimidazolium iodide (HPBI) was developed by quaternization reaction of 1-hexylbenzimidazole and alkyl iodide under solvent-free condition using Teflon-lined, stainless autoclaves. Their thermal properties were measured on the thermo gravimetric analysis and differential scanning calorimeter. The influence of HMBI, HPBI and 1-methyl-3-propylimidazolium iodide (MPII) on redox behavior of I{sub 3}{sup -} and I{sup -} was investigated by cyclic voltammetry and electrochemical impedance spectroscopy. It was found that the resulting HMBI and HPBI had high purity and the reaction time was shortened to 3 h. The thermal stability of HMBI and HPBI was better than that of alkylimidazolium iodides, and HMBI and HPBI were prone to exhibit the supercooling phenomena. The DSCs with HMBI, HPBI and MPII gave photoelectric conversion efficiency of 5.49%, 5.34% and 5.54%, respectively. (author)

  9. Silver clusters and chemistry in zeolites

    SciTech Connect

    Sun, T.; Seff, K. . Dept. of Chemistry)

    1994-06-01

    The spectroscopic work done on silver clusters trapped in solid noble gas matrices at low temperature has been extensively reviewed by Ozin, and Henglein has done the same for photochemical studies of colloidal silver particles in solution. This article will review the chemistry of silver in zeolite hosts, including the synthesis and structures of silver clusters. 127 refs.

  10. Rethinking Schools and the Power of Silver

    ERIC Educational Resources Information Center

    Sleeter, Christine

    2011-01-01

    This 25th anniversary of "Rethinking Schools" can be thought of as its silver anniversary. Silver itself must be considered through contrasting lenses. On the one hand, as lessons in "Rethinking Globalization" teach, silver and gold were the basis of Europe's horrendous exploitation of Latin America. On the other hand, silver is often associated…

  11. Aging of Iodine-Loaded Silver Mordenite in NO2

    SciTech Connect

    Bruffey, Stephanie H.; Jubin, Robert Thomas; Patton, Kaara K.; Walker Jr, Joseph Franklin

    2014-04-01

    Used nuclear fuel facilities need to control and minimize radioactive emissions. Off-gas systems are designed to remove radioactive contaminants, such as 85Kr, 14C, 3H, and 129I. In an off-gas system, any capture material will be exposed to a gas stream for months at a time. This gas stream may be at elevated temperature and could contain water, NOx gas, or a variety of other constituents comprising the dissolver off-gas stream in a nuclear fuel reprocessing plant. For this reason, it is important to evaluate the effects of long-term exposure, or aging, on proposed capture materials. One material under consideration is reduced silver mordenite (Ag0Z), which is recognized for its efficient iodine capture properties. Iodine is immobilized on Ag0Z as AgI, a solid with low volatility (m.p. ≥ 500°C). The aim of this study was to determine whether extended aging at elevated temperature in a nominally 2% NO2 environment would result in a loss of immobilized iodine from this material due to either physical or chemical changes that might occur during aging. Charges of iodine-loaded reduced silver mordenite (I2-Ag0Z) were exposed to a 2% NO2 environment for 1, 2, 3, and 4 months at 150°C, then analyzed for iodine losses The aging study was completed successfully. The material did not visibly change color or form. The results demonstrate that no significant iodine loss was observed over the course of 4 months of 2% NO2 aging of I2-Ag0Z at elevated temperature within the margin of error and the variability (~10%) in the loading along the beds. This provides assurance that iodine will remain immobilized on Ag0Z during extended online use in an off-gas capture treatment system. Future tests should expose I2-Ag0Z to progressively more complex feed gases in an effort to accurately replicate the conditions expected in a reprocessing facility.

  12. Thermal stability of PLD grown silver nanoparticles

    NASA Astrophysics Data System (ADS)

    Shokeen, Poonam; Jain, Amit; Kapoor, Avinashi

    2016-05-01

    Present work discusses the stability of silver nanoparticles at different annealing temperatures. Air muffle furnace annealing is performed to study the thermal stability of pulsed laser deposited silver nanoparticles. Silver reacts with atmospheric oxygen to form silver oxide at annealing temperatures below 473K and thermal decomposition of silver oxide takes place at temperatures above 473K. Oxide formation results in core shrinkage of silver, which in turn affects the surface plasmon resonance of silver nanoparticles. With increase in annealing temperature, the surface plasmon effect of nanoparticles starts to fade. SEM, XRD and UV-vis spectroscopy have been performed to analysis various structural and optical properties.

  13. Superoxide Production by a Manganese-Oxidizing Bacterium Facilitates Iodide Oxidation

    PubMed Central

    Li, Hsiu-Ping; Daniel, Benjamin; Creeley, Danielle; Grandbois, Russell; Zhang, Saijin; Xu, Chen; Ho, Yi-Fang; Schwehr, Kathy A.; Kaplan, Daniel I.; Santschi, Peter H.; Hansel, Colleen M.

    2014-01-01

    The release of radioactive iodine (i.e., iodine-129 and iodine-131) from nuclear reprocessing facilities is a potential threat to human health. The fate and transport of iodine are determined primarily by its redox status, but processes that affect iodine oxidation states in the environment are poorly characterized. Given the difficulty in removing electrons from iodide (I−), naturally occurring iodide oxidation processes require strong oxidants, such as Mn oxides or microbial enzymes. In this study, we examine iodide oxidation by a marine bacterium, Roseobacter sp. AzwK-3b, which promotes Mn(II) oxidation by catalyzing the production of extracellular superoxide (O2−). In the absence of Mn2+, Roseobacter sp. AzwK-3b cultures oxidized ∼90% of the provided iodide (10 μM) within 6 days, whereas in the presence of Mn(II), iodide oxidation occurred only after Mn(IV) formation ceased. Iodide oxidation was not observed during incubations in spent medium or with whole cells under anaerobic conditions or following heat treatment (boiling). Furthermore, iodide oxidation was significantly inhibited in the presence of superoxide dismutase and diphenylene iodonium (a general inhibitor of NADH oxidoreductases). In contrast, the addition of exogenous NADH enhanced iodide oxidation. Taken together, the results indicate that iodide oxidation was mediated primarily by extracellular superoxide generated by Roseobacter sp. AzwK-3b and not by the Mn oxides formed by this organism. Considering that extracellular superoxide formation is a widespread phenomenon among marine and terrestrial bacteria, this could represent an important pathway for iodide oxidation in some environments. PMID:24561582

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

    NASA Astrophysics Data System (ADS)

    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).

  15. Retiring the Silver Bullet

    SciTech Connect

    Lasure, Linda L.

    2006-01-01

    Over the past few decades, advances in biology and electronics have resulted in an enormous increase in the screening rate of new compounds and in the capacity to synthesize vast numbers of new compounds. The understanding of disease has greatly improved. At the same time, the number of targets (or diseases) for the silver bullets has also increased. Yet, the belief that we have to screen enormous numbers of compounds to find the next new drug continues. Today, disease is understood to be a complex interaction of many systems. This ought to cause us to change our paradigm, but it has not. The fundamental reason for the apparent failure of our drug discovery and development research is that we are operating under the constraints of an out-of-date paradigm. The silver-bullet paradigm has always been a myth. Now is the time to debunk the myth and change the paradigm. Our other option is to continue on as we are and accept that the United States will become obsolete on the playing field of drug discovery.

  16. A Silver DNAzyme.

    PubMed

    Saran, Runjhun; Liu, Juewen

    2016-04-01

    Silver is a very common heavy metal, and its detection is of significant analytical importance. DNAzymes are DNA-based catalysts; they typically recruit divalent and trivalent metal ions for catalysis. Herein, we report a silver-specific RNA-cleaving DNAzyme named Ag10c obtained after six rounds of in vitro selection. Ag10c displays a catalytic rate of 0.41 min(-1) with 10 μM Ag(+) at pH 7.5 with 200 mM NaNO3, while its activity is completely inhibited with the same concentration of NaCl. Ag10c is highly specific for Ag(+) among all the tested metals. A catalytic beacon biosensor is designed by labeling a fluorophore and a quencher on the DNAzyme. Fluorescence enhancement is observed in the presence of Ag(+) with a detection limit of 24.9 nM Ag(+). The sensor shows a similar analytical performance in Lake Huron water. This is the first monovalent transition metal dependent RNA-cleaving DNAzyme. Apart from its biosensor application, this study strengthens the idea of exploring beyond the traditional understanding of multivalent ion dependent DNAzyme catalysis. PMID:26977895

  17. Process for making silver metal filaments

    DOEpatents

    Bamberger, Carlos E.

    1997-01-01

    A process for making silver metal particles from silver salt particles having the same morphology. Precursor silver salt particles selected from the group consisting of silver acetate and silver sulfide having a selected morphology are contained in a reactor vessel having means for supporting the particles in an air suspension to prevent the agglomeration of the particles. Air is flowed through the reactor vessel at a flow rate sufficient to suspend the particles in the reactor vessel. The suspended precursor silver salt particles are heated to a processing temperature and at a heating rate below which the physical deterioration of the suspended precursor silver salt particles takes place. The suspended precursor silver salt particles are maintained at the processing temperature for a period of time sufficient to convert the particles into silver metal particles having the same morphology as the precursor silver salt particles.

  18. Process for making silver metal filaments

    SciTech Connect

    Bamberger, C.E.

    1997-05-06

    A process is disclosed for making silver metal particles from silver salt particles having the same morphology. Precursor silver salt particles selected from the group consisting of silver acetate and silver sulfide having a selected morphology are contained in a reactor vessel having means for supporting the particles in an air suspension to prevent the agglomeration of the particles. Air is flowed through the reactor vessel at a flow rate sufficient to suspend the particles in the reactor vessel. The suspended precursor silver salt particles are heated to a processing temperature and at a heating rate below which the physical deterioration of the suspended precursor silver salt particles takes place. The suspended precursor silver salt particles are maintained at the processing temperature for a period of time sufficient to convert the particles into silver metal particles having the same morphology as the precursor silver salt particles. 1 fig.

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

    SciTech Connect

    McGregor, Douglas S.; Ariesanti, Elsa; Corcoran, Bridget

    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.

  20. Project Overview: Inhibition of the Sodium-Iodide Symporter by Perchlorate: Evaluation of Lifestage Sensitivity Using PBPK Modeling

    EPA Science Inventory

    Perchlorate (ClO4-) competitively inhibits uptake of iodide by the sodium-iodide symporter (NIS) in laboratory animals and humans. NIS is found in many tissues, but is primarily responsible for sequestering iodide into the thyroid, enabling biosynthesis of thyroid hormones. The N...

  1. Polymer glazing for silver mirrors

    SciTech Connect

    Neidlinger, H H; Schissel, P

    1985-07-01

    This paper reports on an evaluation and modification of polymeric glazings to protect silver mirrors. The mirrors were made using Corning 7809 glass as a substrate onto which a thin silver film is deposited. The modified polymeric films are then cast from solution onto the silver. The mirrors were characterized by measuring the hemispherical reflectance and the specular reflectance at 660 nm and selected acceptance angles (7.5 mrad or 3.5 mrad). The mirrors were exposed to environmental degradation using accelerated weathering devices and outdoor exposure. Empirical evidence has demonstrated that polymethylmethacrylate is a stable polymer in a terrestrial environment, but the polymer does not provide adequate protection for the silver reflector. The crucial role in degradation played by ultraviolet (uv) light is shown by several experimental results. It has been demonstrated that uv stabilizers added to the polymer improve the weatherability of mirrors. The relative effectiveness of different stabilizers will be discussed in terms of the weathering modes, retention of optical properties, and effectiveness of the additives. The process for silver deposition influences the reflectance of silver mirrors, and the optical properties depend on subtle relationships between the metallization and the dielectric (polymeric) films that are in contact with the silver.

  2. MOD silver metallization for photovoltaics

    NASA Technical Reports Server (NTRS)

    Vest, G. M.; Vest, R. W.

    1985-01-01

    The feasibility of utilizing metallo-organic decomposition (MOD) silver inks were investigated for front contact metallization of solar cells. Generic synthesis procedures were developed for all metallo-organic compounds investigated. Silver neodecanoate was found to be the most suitable silver metallo-organic compound for use in thick film inks, but the quality of the inks was found to be highly dependent on its purity. Although neither the process nor inks were completely optimized for solar cell front contact metallization, they show great promise for this application.

  3. Coincidence Efficiency of Sodium Iodide Detectors for Positron Annihilation

    NASA Astrophysics Data System (ADS)

    Eckert, Thomas; Vincett, Laurel; Yuly, Mark; Padalino, Stephen; Russ, Megan; Bienstock, Mollie; Simone, Angela; Ellison, Drew; Desmitt, Holly; Sangster, Craig; Regan, Sean

    2014-10-01

    One possible diagnostic technique for characterizing inertial confinement fusion reactions uses tertiary neutron activation of 12C via the 12C(n, 2n)11C reaction. A recent experiment to measure this cross section involved counting the positron annihilation gamma rays from the 11C decay by using sodium iodide detectors in coincidence. To determine the number of 11C decays requires an accurate value for the full-peak coincidence efficiency for the detector system. A new technique has been developed to measure this coincidence efficiency by detecting the positron prior to its annihilation, and vetoing events in which decay gamma rays other than the 511 keV annihilation gamma rays could enter the detectors. Measurements and simulation results for the absolute coincidence total and full-peak efficiencies are presented. Funded in part by a grant from the DOE through the Laboratory for Laser Energetics.

  4. Photon recycling in lead iodide perovskite solar cells.

    PubMed

    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

    2016-03-25

    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. PMID:27013728

  5. Photon recycling in lead iodide perovskite solar cells

    NASA Astrophysics Data System (ADS)

    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.

  6. Modified purification of mercuric iodide for crystal growth

    NASA Astrophysics Data System (ADS)

    Skinner, N. L.; Ortale, C.; Schieber, M. M.; Van Den Berg, L.

    1988-06-01

    The standard procedure used in our laboratory to purify commercially available mercuric iodide (HgI 2) consists of a sequence of steps: (1) repeated sublimation under continuous evacuation, followed by (2) melting and recrystallization, and (3) a sublimation process in a closed tube. This paper describes a modification of the standard purification sequence by adding recrystallization of the HgI 2 in hydrochloric acid. Leaching cation impurities out of HgI 2 powder with hydrochloric acid has been practised before by Zaletin et al. Our objective for the hydrochloric acid treatment was to remove nitrates and hydrocarbons which were interfering with the vapor transport during crystal growth. Results of the procedure are presented in terms of total carbon and selected ion content of the treated and untreated material.

  7. Investigation of copper electrodes for mercuric iodide detector applications

    NASA Astrophysics Data System (ADS)

    Bao, X. J.; Schlesinger, T. E.; James, R. B.; Stulen, R. H.; Ortale, C.; van den Berg, L.

    1990-06-01

    Copper diffusion in mercuric iodide was studied by low-temperature photoluminescence (PL) spectroscopy and Auger electron spectroscopy. A broad radiative emission band at a wavelength of about 6720 Å in the PL spectra was found to be related to Cu incorporation in the crystal. PL spectra obtained from surface doping experiments indicate that Cu is a rapid diffuser in HgI2 bulk material. Auger electron spectroscopy performed as a function of depth from the crystal surface confirms the rapid bulk diffusion process of Cu in HgI2. Fabrication of HgI2 nuclear detectors with Cu electrodes indicates that Cu is not acceptable as an electrode material, which is consistent with the fact that it diffuses easily into the bulk crystal and introduces new radiative recombination centers.

  8. Incorporation of defects during processing of mercuric iodide detectors

    NASA Astrophysics Data System (ADS)

    Bao, X. J.; Schlesinger, T. E.; James, R. B.; Stulen, R. H.; Ortale, C.; Cheng, A. Y.

    1990-07-01

    The effects of chemical etching in KI solution, heating, and vacuum exposures of HgI2 were individually studied by low-temperature photoluminescence (PL) spectroscopy. Each of these processing steps is important in the manufacturing of mercuric iodide detectors and may be responsible for the incorporation of carrier traps both in the near-surface region and in the bulk. The results of etching experiments showed that the near-surface region has a different defect structure than the bulk, which appears to result from iodine deficiency. Bulk heating at 100 °C also modifies the defect structure of the crystal. Vacuum exposure has an effect similar to chemical etching, but it does not cause significant degradation of the stoichiometry for recently KI-etched specimens. These studies suggest that some features in the PL spectra of HgI2 are associated with stoichiometry of the specimens.

  9. Elemental impurity analysis of mercuric iodide by ICP/MS

    SciTech Connect

    Cross, E.S.; Mroz, E.; Olivares, J.A.

    1994-06-01

    A method has been developed to analyze mercuric iodide (HgI{sub 2}) for elemental contamination using Inductively Coupled Plasma/Mass Spectroscopy (ICP/MS). This paper discusses the ICP/MS method, the effectiveness of purification schemes for removing impurities from HgI{sub 2}, as well as preliminary correlations between HgI{sub 2} detector performance and elemental contamination levels. The purified HgI{sub 2} is grown into a single crystal by physical vapor transport. The crystal are cut into slices and they are fabricated into room temperature radiation detectors and photocells. Crystals that produce good resolution gamma detector do not necessarily make good resolution photocells or x-ray detectors. Many factors other than elemental impurities may contribute to these differences in performance.

  10. Hybrid Perovskite Solar Cells with Copper Iodide as Hole Transportlayer

    NASA Astrophysics Data System (ADS)

    Haroldson, Ross; Olds, Zane; Cook, Alexander B.; Zakhidov, Anvar

    2015-03-01

    Hybrid organo-metallic solar cells based on perovskite-structured nanocrystals have had steadily improving power conversion efficiencies over the past several years, and within this short period of time are capable of achieving efficiencies over 19%. In our work we show that dopantsa thin layer of Copper Iodide (CuI) on top of a hole transport layer such as PEDOT:PSS increases the open circuit voltage, of the devices. CuI is a p-type hole conducting material with a large band gap that has been used before for hole transport layers by itself. We demonstrate that CuI as the working hole transport layer increases the Voc about 10% increase.

  11. Instrument Development and Gamma Spectroscopy with Strontium Iodide

    SciTech Connect

    Cherepy, Nerine; Payne, Stephen A.; Sturm, Benjamin; Drury, Owen; O’Neal, S P; Thelin, P; Shah, Kanai; Hawrami, Rastgo; Momayezi, M; Hurst, B.; Wiggen, B.; Bhattacharya, P.; Burger, Arnold; Boatner, Lynn A; Ramey, Joanne Oxendine

    2012-01-01

    Development of the Europium-doped Strontium Iodide scintillator, SrI2(Eu), involves advances in crystal growth, optics and readout methodology for prototype detectors. We have demonstrated energy resolution of 3% at 662 keV for a 26 cm3 SrI2(Eu) crystal, which is comparable to the performance obtained with Cerium-doped Lanthanum Bromide of equivalent size. Compared to standard analog readout, use of a digital readout method allows improved energy resolution to be obtained with large-volume SrI2(Eu) crystals. Comparative gamma spectra acquired with LaBr3(Ce) and NaI(Tl) quantitatively depict the value of the high resolution and low intrinsic radioactivity of SrI2(Eu) in discriminating closely spaced gamma lines for radioisotope identification applications.

  12. Cost-benefit analysis of potassium iodide distribution programs

    SciTech Connect

    Aldrich, D.C.

    1982-01-01

    An analysis has been performed to provide guidance to policymakers concerning the effectiveness of potassium iodide (KI) as a thyroid blocking agent in potential reactor accident situations, the distance to which (or area within which) it should be distributed and its relative effectiveness compared to other available protective measures. The analysis was performed using the Reactor Safety Study (WASH-1400) consequence model. Four categories of accidents were addressed: gap activity release accident (GAP), GAP without containment isolation, core melt with a melt-through release, and core melt with an atmospheric release. Cost-benefit ratios (US $/thyroid nodule prevented) are given assuming that no other protective measures are taken. Uncertainties due to health effects parameters, accident source terms, accident probabilities and costs are assessed. The effects of other potential protective measures, such as evacuation and sheltering, and the impact on children (critical population) are evaluated.

  13. High temperature infrared spectrum of sodium iodide (NaI)

    NASA Astrophysics Data System (ADS)

    Maki, Arthur G.

    2014-09-01

    The absorption spectrum of sodium iodide vapor between 200 and 275 cm-1 has been measured with a resolution of 0.006 cm-1 at a temperature of 1096 K. The Δv = 1 transitions from v = 1 ← 0 to v = 13 ← 12 have been measured. Dunham constants are given from an least-squares analysis of 1285 fairly well resolved transitions. The band center for the fundamental band is ν0 = 257.2837 ± 0.0002 cm-1. The relative intensities of the Δv = 1 transitions from different vibrational states are studied and it is shown that the intensity is roughly proportional to v″ + 1 as expected from the harmonic oscillator approximation. From measurements of the Herman-Wallis constant, α1,0 = -0.0054 ± 0.0008, it is estimated that the transition moment must be μ1,0 ≈ 0.135 ± 0.020 debye.

  14. Mercuric Iodide Photocell Technology for Room Temperature Readout of Scintillators

    SciTech Connect

    Warnick Kernan et al.

    2007-08-31

    Mercuric iodide (HgI2) is a well known material for the direct detection of gamma rays; however, the largest volume achievable is limited by thickness of the detector, which needs to be a small fraction of the average trapping length for electrons. We are reporting here preliminary results in using HgI2 crystals to fabricate photocells used in the readout of various scintillators. The optical spectral response and efficiency of these photocells were measured and will be reported. Preliminary nuclear response from a HgI2 photocell that was optically matched to a Ce3+ :LaBr3 scintillator will also be presented and discussed. Further improvements will be sought by optimizing the transparent contact technology.

  15. Coulomb Screening and Coherent Phonon in Methylammonium Lead Iodide Perovskites.

    PubMed

    Wang, He; Valkunas, Leonas; Cao, Thu; Whittaker-Brooks, Luisa; Fleming, Graham R

    2016-08-18

    Methylammonium lead iodide (CH3NH3PbI3) hybrid perovskite in the tetragonal and orthorhombic phases have different exciton binding energies and demonstrate different excitation kinetics. Here, we explore the role that crystal structure plays in the kinetics via fluence dependent transient absorption spectroscopy. We observe stronger saturation of the free carrier concentration under high pump energy density in the orthorhombic phase relative to the tetragonal phase. We attribute this phenomenon to small dielectric constant, large exciton binding energy, and weak Coulomb screening, which results in difficult exciton dissociation under high light intensity in the orthorhombic phase. At higher excitation intensities, we observe a coherent phonon with an oscillation frequency of 23.4 cm(-1) at 77 K, whose amplitude tracks the increase of the first-order lifetime. PMID:27485190

  16. Improvement in thallium hydride generation using iodide and Rhodamine B.

    PubMed

    Picón, David; Carrero, Pablo; Valero, Maribel; de Peña, Yaneira Petit; Gutiérrez, Luís

    2015-05-01

    A continuous flow hydride generation atomic absorption spectrometry (CF-HG-AAS) system was used to study the enhancement effect of different substances for conventional chemical HG of thallium. At room temperature, the acidified sample solution containing the respective enhancement reagent merged with the aqueous NaBH4 solution. The generated thallium hydride was stripped from the eluent solution by the addition of a nitrogen flow and thereafter the bulk phases were separated in a gas-liquid separator. The main factors under study were concentration and type of enhancement reagent (Te, iodide added as KI, Rhodamine B, malachite green and crystal violet) and acid (HCl, H2SO4 or HNO3). Other parameters affecting the thallium hydride generation, such as: NaBH4 concentration, carrier gas flow rate, length of reaction-mixing coil and reagents flow rates, were studied and optimized. Among the enhancement reagents tested, the combination of Rhodamine B and iodide produced the best results. A linear response was obtained between the detection limit (LOD (3σ)) of 1.5μg L(-1) and 1000μg L(-1). The RSD% (n=10) for a solution containing 15μg L(-1) of Tl was 2.9%. The recoveries of thallium in environmental water samples by spiking the samples with 10 and 20µg L(-1) of Tl were in the 97.0-102.5% range. The accuracy for Tl determination was further confirmed by the analysis of a water standard reference material (1643e form NIST, USA). Finally, it was demonstrated that malachite green and crystal violet showed similar enhancement effect like Rhodamine B for thallium HG. PMID:25702995

  17. Rapid sonochemical preparation of shape-selective lead iodide

    SciTech Connect

    Huang, Baojun; He, Qin; Fa, Wenjun; Li, Pinjiang; Zhang, Yange; Zheng, Zhi

    2012-09-15

    Graphical abstract: SEM morphologies of various PbI2 products obtained with the iodine concentration of 6.7 g/L and irradiation time of 1 minute at the reaction temperatures of 35 °C (a), 25 °C (b), and 15 °C (c). Highlights: ► PbI{sub 2} with various morphologies were rapidly formed at room temperature. ► We could well control the morphologies of PbI{sub 2} by changing reaction conditions. ► The PbI{sub 2} films could better resist rolling in a liquid media. -- Abstract: Lead iodide (PbI{sub 2}) films/crystals with various nano/micro morphologies (e.g., Nanoflake, block and microrod) were rapidly synthesized by taking advantage of a simple sonochemical method. The PbI{sub 2} crystals with uniform nanoflake structures could be fabricated directly on lead foils with the irradiation time as short as 36 s via interfacial reaction between lead foils and elemental iodine in ethanol at ambient temperature. It was found experimentally that the morphologies of the resulting thin films/crystals could be well controlled by the adjustment of several parameters including irradiation time, reaction solvents, iodine concentration, ultrasonic power, and reaction temperature. Most importantly, the resultant PbI{sub 2} films are stable enough to resist rolling under the drastic ultrasound irradiation in a liquid media. This method is believed to be the fastest way for in situ fabrication of morphology-controlled semiconductor films on various metal substrates for subsequent applications related to the other metal iodide or metal sulfide semiconductor films.

  18. In Vivo Evaluation of Transdermal Iodide Microemulsion for Treating Iodine Deficiency Using Sprague Dawley Rats.

    PubMed

    Alayoubi, Alaadin; Sullivan, Ryan D; Lou, Hao; Patel, Hemlata; Mandrell, Timothy; Helms, Richard; Almoazen, Hassan

    2016-06-01

    The objective of this study was to evaluate the transdermal efficiency of iodide microemulsion in treating iodine deficiency using rats as an animal model. Animals were fed either iodine-deficient diet (20 μg/kg iodide) or control diet (200 μg/kg iodide) over a 17-month period. At month 14, iodide microemulsion was applied topically in iodine-deficient group and physiological evaluations of thyroid gland functions were characterized by monitoring the thyroid hormones (T3, T4), thyroid-stimulating hormone (TSH), iodide ion excretion in urine, and the overall rat body weights in both groups. Moreover, morphological evaluations of thyroid gland before and after treatment were performed by ultrasound imaging and through histological assessment. Prior to microemulsion treatment, the levels of T3, T4, and TSH in iodine-deficient group were statistically significant as compared to that in the control group. The levels of T3 and T4 increased while TSH level decreased significantly in iodine-deficient group within the first 4 weeks of treatment. After treatment, iodide concentration in urine increased significantly. There was no statistical difference in weight between the two groups. Ultrasound imaging and histological evaluations showed evidence of hyperplasia in iodine-deficient group. Topical iodide microemulsion has shown a promising potential as a novel delivery system to treat iodine deficiency. PMID:26288943

  19. Determination of silver, bismuth, cadmium, copper, lead, and zinc in geologic materials by atomic absorption spectrometry with tricaprylylmethylammonium chloride

    USGS Publications Warehouse

    Viets, J.G.

    1978-01-01

    Interferences commonly encountered in the determination of silver, bismuth, cadmium, copper, lead, and zinc at crustal abundance levels are effectively eliminated using a rapid, sensitive, organic extraction technique. A potassium chlorate-hydrochloric acid digestion solubilizes the metals not tightly bound in the silicate lattice of rocks, soils, and stream sediments. The six metals are selectively extracted into a 10% Aliquat 336-MIBK organic phase in the presence of ascorbic acid and potassium iodide. Metals in the organic extract are determined by flame atomic absorption spectrometry to the 0.02-ppm level for silver, cadmium, copper, and zinc and to the 0.2-ppm level for bismuth and lead with a maximum relative standard deviation of 18.8% for known reference samples. An additional hydrofluoric acid digestion may be used to determine metals substituted in the silicate lattice.

  20. Modeling the effect of iodide distribution on ozone deposition to seawater surface

    NASA Astrophysics Data System (ADS)

    Oh, In-Bo; Byun, Daewon W.; Kim, Hyun-Cheol; Kim, Soontae; Cameron, Bob

    Spatial changes in the dry deposition of ozone to the sea surface associated with ozone uptake by the dissolved iodide ions were analyzed in the northwestern Gulf of Mexico using the Community Multiscale Air Quality Model (CMAQ). The dry deposition module in CMAQ was modified using a formula developed by Chang et al. [2004. Ozone deposition to the sea surface: chemical enhancement and wind speed dependence. Atmospheric Environment 38, 1053-1059], which accounts for chemical enhancement by iodide reacting with ozone in seawater. In addition, an attempt was made to incorporate iodide concentrations from the satellite-derived estimates of near-surface chlorophyll a concentrations into the CMAQ gridded fields. One-month CMAQ simulations conducted with the modified module including iodide reaction showed a significant increase in the dry deposition velocity of ozone onto the sea surface, especially Texas and Louisiana Coast corresponding to the area with high iodide concentrations. On average, about 70% enhancement of ozone dry deposition velocity over the seawater was attributed to the iodide effect alone and the rest is mostly due to the effects of wind. The enhanced deposition velocity by iodide effect led to the marked increase in dry deposition amounts mostly near the coast, resulting in some changes in ambient ozone concentration. Interestingly, a small decrease in deposition amounts was found just inland from the shoreline, indicating that the iodide interaction can also affect ozone concentration in the inland coastal area. An in-depth analysis of a 2-day simulation showed the iodide effects on changes in the spatiotemporal distributions of the ozone deposition and concentration, which are highly dependent on coastal winds.

  1. Thyroid iodide compartments and their implication in the rat thyroid iodine organification

    SciTech Connect

    Bastiani, P.; Simon, C.

    1982-05-01

    To estimate the relative participation of transported and intrathyroidally generated iodide (internal iodide) in the iodination of newly synthesized and preexisting thyroglobulin (Tg) in the rat thyroid, the specific radioactivities (SRAs) of thyroid iodide, Tg, lysosomal iodine, and plasma hormones were followed for 92 h after radioactive iodide injection in intact or hypophysectomized rats. In control rats, the SRA of Tg and lysosomal iodine reached a maximum at 12 h. However, the SRA of lysosomal iodide was always smaller than that of Tg. In contrast, the SRA of hormonal iodide attained a maximum at 48 h. Thus, newly labeled iodine is endocytosed and mixed inside the lysosomes with older previously iodinated molecules; hormone secretion is mainly due to old labeled iodine (i.e. iodine with a high SRA from 48-96 h). These results are consistent with the presence of least two Tg compartments, with different turnover rates and hormone contents. On the other hand, in hypophysectomized rats, the SRA of Tg, lysosomes, and hormones showed only one maximum, at 24 h. Furthermore, the SRAs of Tg and lysosomes were similar at each time interval. It is inferred that in such rats, the old labeled iodine compartment is strongly reduced, and that inside the lysosomes, newly labeled iodine is predominant. Since in hypophysectomized rats, the recycling of iodide is abolished, it is concluded that in normal rats: 1) transported iodide is organified mainly by direct iodination of newly synthesized Tg, independently of TSH, and 2) internal iodide is organified mainly by delayed iodination of preexisting Tg, this process being TSH dependent.

  2. Silver Nafion for Thermogalvanic Applications

    NASA Astrophysics Data System (ADS)

    Chang, William; Popere, Bhooshan; Evans, Chris; Russ, Boris; Segalman, Rachel

    2015-03-01

    Thermogalvanics convert a temperature gradient, typically from waste heat, into electrical power using a reversible electrochemical reaction. The conversion efficiency in thermogalvanics, like with thermoelectrics, are governed by the Seebeck coefficient, the carrier conductivity and the thermal conductivity of the material. We demonstrate that the material systems silver Nafion and silver poly-styrenesulfonate are air-stable, water processable materials that demonstrate extremely high Seebeck coefficients and moderate carrier conductivities. These power factors, when coupled with the low thermal conductivities inherent in polymers, results in materials with excellent thermogalvanic figure of merits. We show the dependence of these three material properties to material composition and processing. In this talk, we show how the Seebeck coefficient in silver Nafion and silver polystyrene-sulfonate are opposite in sign, allowing construction of a thermogalvanic device. With these ion conductors, we hope to open up a flexible pathway to waste heat recovery using materials typically studied for electrochemical applications.

  3. TADF for singlet harvesting: next generation OLED materials based on brightly green and blue emitting Cu(I) and Ag(I) compounds

    NASA Astrophysics Data System (ADS)

    Yersin, Hartmut; Leitl, Markus J.; Czerwieniec, Rafal

    2014-10-01

    Detailed photophysical studies are presented for Cu2Cl2(dppb)2 and Ag2Cl2(dppb)2. Both compounds show very effective thermally activated delayed fluorescence (TADF) at ambient temperature with an emission quantum yield of the Ag(I) complex of ΦPL(300 K) = 93 %. This emission is blue shifted by 65 nm (2500 cm-1) with respect to the emission of the Cu(I) complex, demonstrating a valuable strategy for engineering blue light emitters. Potentially, these materials are well suited for taking advantage of the singlet harvesting effect in an OLED device. Moreover, both compounds do not show effects of concentration quenching at high emitter concentration, a property which might be attractive for reducing the efficiency roll-off at higher current densities. Investigations down to T = 1.6 K show that spin-orbit coupling (SOC) is particularly weak. This is displayed in the very long emission decay times of the triplet states (T1 states) of metal-toligand charge transfer (3MLCT) character, amounting to τ(Ag2Cl2(dppb)2) = 1.1 ms and τ(Cu2Cl2(dppb)2) = 2.2 ms. According to the TADF mechanism, which leads to the additional decay channel at ambient temperature via the S1 state (of 1MLCT character), an increase of the radiative rate by a factor of 70 and almost 500 for Ag2Cl2(dppb)2 and Cu2Cl2(dppb)2, respectively, is induced. This results in radiative rates at ambient temperature of kr = 6.2 • 104 s-1 (τr = 16 μs, Ag(I) complex) and 11.7 • 104 s-1 (τr = 8.5 μs, Cu(I) complex). Simple approaches are presented that allow us to understand the weakness of SOC on the basis of results from DFT and TD-DFT calculations. Investigations of the emission decay properties down to T = 1.6 K further support the conclusions with respect to the SOC strength.

  4. Methyl iodide as a promoter of the SCC of zirconium alloys in iodine vapour

    NASA Astrophysics Data System (ADS)

    Cox, B.; Haddad, R.

    1986-01-01

    The presence of organic-iodine contaminants, or specifically methyl iodide, in the iodine environment during stress corrosion tests leads to an increased frequency of crack nucleation, and possibly a more rapid crack propagation process. The unusual fractographic features associated with these impurities suggest that they enhance the reduction in the surface energy of zirconium, cause an instability in the propagating crack front, and possibly enhance the rate of reaction to form zirconium iodides. These impurities are the most potent catalysts of iodine-induced cracking so far identified, although methyl iodide alone cannot initiate cracking.

  5. Selective recognition iodide in aqueous solution based on fluorescence enhancement chemosensor

    NASA Astrophysics Data System (ADS)

    Lin, Li-Rong; Fang, Wei; Yu, Yun; Huang, Rong-Bin; Zheng, Lan-Sun

    2007-08-01

    A novel and simple fluorescence enhancement method for selectively sensing iodide was proposed based on metal complex formation between mercuric(II) ion with fluorophore ( p-((dimethylamino)benzylidene)thiosemicarbazide, 1) and with anion in aqueous solution. The 1-Hg complex was found to show selectively and sensitively fluorescence enhancement response toward iodide over than S 2-, EDTA, SCN -, CH 3CO 2-, Br -, Cl -, F -, H 2PO 4- and SO 42-, which was attributed to the higher stability of inorganic complex between iodide and mercuric(II).

  6. Permeability of iodide in multilamellar liposomes modeled by two compartments and a reservoir.

    PubMed

    Schullery, S E

    1977-07-14

    A previously published rate law for the diffusion of iodide from multilamellar egg phosphatidylcholine liposomes (Schullery, S.E. (1975) Chem. Phys. Lipids 14, 49-58) is fitted to the relatively simple mathematical model of two compartments in series with a reservoir. All of the inner liposome compartments are assumed to behave as effectively one compartment in series with the liposome's outermost compartment. Based on this model, reasonable values are calculated for the fraction of the total solution trapped by liposomes which is in the outermost liposome compartment, 17%, and the permeability coefficient of iodide against isotonic, mixed iodide-chloride solution, 2-10(-9) cm/s. PMID:884087

  7. Investigations on electrical and electrochemical properties of Ag+ ion conducting quaternary solid electrolyte systems: x[0.75 AgI : 0.25 AgCl] : (1-x)RbI

    NASA Astrophysics Data System (ADS)

    Agrawal, R. C.; Chandra, Angesh; Bhatt, Alok; Mahipal, Y. K.

    2007-08-01

    Investigations on ion transport behaviour of new Ag+ ion conducting quaternary solid electrolyte systems: x[0.75AgI : 0.25AgCl] : (1 - x)RbI, where 0.1 <= x <= 1 mol.wt fractions, are reported. The solid electrolyte systems were synthesized adopting different routes of solid solution reactions. An alternative host salt, 'a quenched [0.75AgI : 0.25AgCl] mixed system solid solution', discovered at the present laboratory, has been used in place of AgI. The compositional dependent conductivity studies at room temperature revealed the quaternary systems 0.7[0.75AgI : 0.25AgCl] : 0.3RbI as the optimum conducting composition (OCC). AgI has been traditionally and most widely used as host salt in the past to prepare the majority of well-known fast Ag+ ion conductors including the ternary superionic solids MAg4I5 (M = Rb, K, NH4). Also, RbAg4I5 has been recognized as one of the highest conducting superionic solids with conductivity σrt ~ 10-1 S cm-1 at room temperature. However, it has been observed that RbAg4I5 is thermodynamically unstable, particularly in the open ambient conditions, while the newly synthesized quaternary solid electrolyte, having OCC 0.7[0.75AgI : 0.25AgCl] : 0.3RbI, has been observed to be much more stable than RbAg4I5. For direct comparison of the ion conduction behaviour of the newly synthesized OCC, the ternary superionic solid RbAg4I5 (0.8AgI : 0.2RbI) has also been synthesized in an identical manner. The room temperature conductivity (σrt) of the newly synthesized quaternary OCC was slightly lower than that of RbAg4I5. However, σrt remained practically stable for a fairly long time in the open ambient conditions as compared with that of RbAg4I5. The mechanism of ion transport in OCC has been characterized on the basis of experimental studies on various ionic parameters namely conductivity (σ), ionic mobility (μ), mobile ion concentration (n), ionic drift velocity (vd), ionic transference number (tion) etc. The temperature dependent studies on

  8. Cu(I) and Ag(I) complexes of 7,10-bis-N-heterocycle-diazafluoranthenes: programmed molecular grids?

    PubMed

    Rahanyan, Nelli; Duttwyler, Simon; Linden, Anthony; Baldridge, Kim K; Siegel, Jay S

    2014-07-28

    Reactions of 7,10-disubstituted diazafluoranthene derivatives with three different silver(I) salts AgX (X = [PF6](-), [SbF6](-), [CB11HCl11](-)) and [Cu(CH3CN)4]PF6 afforded complexes exhibiting five different motifs. The crystal structures of the free ligands and nine new complexes from this series of reactions are reported. The use of 2,5-di-tert-butyl-7,10-di(pyridin-2-yl)-8,9-diazafluoranthene as a ligand leads to the formation of the tetranuclear compounds [Ag4(C32H30N4)4][PF6]4·3C6H6·4MeCN, [Ag4(C32H30N4)4][SbF6]4·4C5H12 and [Cu4(C32H30N4)4][PF6]4·8C3H6O, which exhibit "propeller" and saddle-type geometry, respectively, as well as a dinuclear complex [Ag2(C32H30N4)2][CHB11Cl11]2·4C6H4Cl2·CH2Cl2. The reactions involving the less sterically hindered 2,5-di-tert-butyl-7,10-di-(pyrimidin-2-yl)-8,9-diazafluoranthene and 2,5-di-tert-butyl-7,10-di(thiazol-2-yl)-8,9-diazafluoranthene afforded crystals of the dinuclear complexes [Ag2(C30H28N6)2][PF6]2·0.5CH2Cl2·0.5C6H5Cl·0.5C6H12, [Ag2(C30H28N6)2][SbF6]2·C3H6O·0.5C6H14·0.5C6H6, the polymeric species [Ag2(C28H26N4S2)2]n·2n[PF6]n·nC3H6O and the tetranuclear compounds [Cu4(C26H25N4S2)4][PF6]4·2CHCl3·2C3H6O and [Cu4(C30H28N6)4][PF6]4·2.17H2O, which possess saddle and grid-like architectures, respectively. Conformational analysis of the free ligands showed that they exhibit N-C-C-N torsion angles ranging from syn clinal (58°) to fully anti-periplanar conformations; the syn clinal conformation dominates in the complexes. The relative energies of the possible structural conformations of the synthesized ligands, as well as of oxazole disubstituted diazafluoranthenes, were calculated using density functional theory at the B97D/Def2-TZVPP level of theory. PMID:24915516

  9. Preliminary flight prototype silver ion monitoring system

    NASA Technical Reports Server (NTRS)

    Brady, J.

    1974-01-01

    The design, fabrication, and testing of a preliminary flight prototype silver ion monitoring system based on potentiometric principles and utilizing a solid-state silver sulfide electrode paired with a pressurized double-junction reference electrode housing a replaceable electrolyte reservoir is described. The design provides automatic electronic calibration utilizing saturated silver bromide solution as a silver ion standard. The problem of loss of silver ion from recirculating fluid, its cause, and corrective procedures are reported. The instability of the silver sulfide electrode is discussed as well as difficulties met in implementing the autocalibration procedure.

  10. Anion-directed assembly and crystal transformation of Ag(I) coordination polymers with a versatile tripyridyltriazole ligand 3,4-bis(2-pyridyl)-5-(4-pyridyl)-1,2,4-triazole

    NASA Astrophysics Data System (ADS)

    Li, Cheng-Peng; Chen, Jing; Guo, Wei; Du, Miao

    2015-03-01

    A series of distinct Ag(I) coordination polymers, namely {[Ag2(L224)(H2O)3](SiF6)(H2O)4}n (1), {[Ag2(L224)2(NO3)](NO3)(H2O)}n (3), {[Ag2(L224)(OOCC6H5)(H2O)](NO3)(H2O)2}n (4), and {[Ag(L224)2](CF3SO3)(H2O)0.25}n (5) have been synthesized by assembling a versatile ligand 3,4-bis(2-pyridyl)-5-(4-pyridyl)-1,2,4-triazole (L224) with different Ag(I) salts. Their diverse 1D and 2D coordination arrays indicate the critical role of counterions in structural assemblies. Interestingly, single-crystal-to-single-crystal (SC-SC) transformation from 1 to {[Ag2(L224)(CF3COO)2(H2O)](H2O)}n (2) will occur in the water solution of Ag(CF3COO). Structural comparison and mechanism of SC-SC transformation are discussed. These Ag(I) coordination polymers show enhanced ligand-based solid-state fluorescent emissions.

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

    NASA Astrophysics Data System (ADS)

    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.

  12. Suppression of thyroid radioiodine uptake by various doses of stable iodide

    SciTech Connect

    Sternthal, E.; Lipworth, L.; Stanley, B.; Abreau, C.; Fang, S.L.; Braverman, L.E.

    1980-11-06

    We studied the effect of various doses of sodium iodide on thyroid radioiodine uptake in euthyroid volunteers by giving single doses of 10, 30, 50, and 100 mg and then daily doses of 10, 15, 30, 50, or 100 mg for 12 days thereafter. All single doses above 10 mg suppressed 24h thyroid uptake of /sup 123/I to 0.7 to 1.5 per cent. Continued daily administration of 15 mg of iodide or more resulted in values consistently below 2 per cent. A small but statistically significant fall in serum thyroxine (T/sub 4/) and triiodothyronine (T/sub 3/) and a rise in serum thyrotropin (TSH) concentrations were observed after eight and 12 days of iodide treatment. This study provides guidelines for stable iodide prophylaxis in the event of exposure to radioactive iodine.

  13. Theoretical investigations of silver clusters and silver-ligand systems.

    SciTech Connect

    Jellinek, J.; Salian, U.; Srinivas, S.

    1999-05-19

    Studies directed at understanding structural and electronic properties of silver clusters have been and remain the subject of an active theoretical [1-22] and experimental [23- 38] effort. One of the reasons is the (still) important role these systems play in the photographic process. Investigations of interactions of silver clusters with different atoms and molecules are motivated primarily by a possible utility of these clusters in catalytic processes. The important role of silver in the selective oxidation of ethylene into ethylene oxide, the feedstock for polyester production, is well-known [39]. Possible variations in chemical reactivity with the cluster size and understanding of the mechanisms of interactions with different ligands may lead to new and more efficient applications. Investigations of cluster-ligand systems also contribute a great deal to a better understanding of gas-surface interactions. Accordingly, theoretical studies of silver clusters and cluster-ligand systems [40-44] fall into two categories--those that use clusters as models for silver surfaces [40], and those that target clusters and cluster-ligand interactions as subjects in their own right [41-44]. The common goal of all these studies is to elucidate the nature of the interatomic interactions and bonding at the microscopic level and thereby arrive at a fundamental understanding and description of the various structural and electronic properties.

  14. Different Coordination Modes of a Tripod Phosphine in Gold(I) and Silver(I) Complexes

    PubMed Central

    Sevillano, P.; Habtemariam, A.; Parsons, S.; Sadler, P. J.

    1999-01-01

    The following gold(I) and silver(I) complexes of the tritertiary phosphine 1,1,1- tris(diphenylphosphinomethyl)ethane, tripod , have been synthesised: Au3(tripod)X3 [X = Cl(1), Br(2), I(3)]; [Au3(tripod)2Cl2]Cl (4); Au(tripod)X [X = Br(5), I(6)]; Ag3(tripod) (NO3)4 (7), Ag(tripod)NO3 (8). They were characterized by X-ray diffraction (complexes 2, 3 and 4), 31P NMR spectroscopy, electrospray and FAB mass spectrometry and infrared spectroscopy. Complexes 2 and 3 show a linear coordination geometry for Au(I), with relatively short Au-P bond distances. Complex 3 has a Au•••Au intramolecular distance of 3.326 A ° , while complex 2 had a short Au•••Au intermolecular interaction of 3.048 A ° . Complexes 4-6 were found by 31P NMR spectroscopy studies to contain a mixture of species in solution, one of which crystallised as [Au3(tripod|)2Cl2]Cl which was shown by X-ray diffraction to contain both tetrahedral and linear Au(I), the first example of a Au(I) complex containing such a mixture of geometries. The reaction of [Au3 (tripod)Cl3] (1) with tripod led successfully to the formation of [Au3(tripod|)2Cl2]+ and [Au3(tripod)2Cl3]+ and [Au3(tripod|)3Cl]2+. The silver(I) complexes, 7 and 8 appear to contain linear and tetrahedral Ag(I), respectively. PMID:18475895

  15. Silver sulfadoxinate: Synthesis, structural and spectroscopic characterizations, and preliminary antibacterial assays in vitro

    NASA Astrophysics Data System (ADS)

    Zanvettor, Nina T.; Abbehausen, Camilla; Lustri, Wilton R.; Cuin, Alexandre; Masciocchi, Norberto; Corbi, Pedro P.

    2015-02-01

    The sulfa drug sulfadoxine (SFX) reacted with Ag+ ions in aqueous solution, affording a new silver(I) complex (AgSFX), which was fully characterized by chemical, spectroscopic and structural methods. Elemental, ESI-TOF mass spectrometric and thermal analyses of AgSFX suggested a [Ag(C12H13N4O2S)] empirical formula. Infrared spectroscopic measurements indicated ligand coordination to Ag(I) through the nitrogen atoms of the (deprotonated) sulfonamide group and by the pyrimidine ring, as well as through oxygen atom(s) of the sulfonamide group. These hypotheses were corroborated by 13C and 15N SS-NMR spectroscopy and by an unconventional structural characterization based on X-ray powder diffraction data. The latter showed that AgSFX crystallizes as centrosymmetric dimers with a strong Ag⋯Ag interaction of 2.7435(6) Å, induced by the presence of exo-bidentate N,N‧ bridging ligands and the formation of an eight-membered ring of [AgNCN]2 sequence, nearly planar. Participation of oxygen atoms of the sulfonamide residues generates in the crystal a 1D coordination polymer, likely responsible for its very limited solubility in all common solvents. Besides the analytical, spectroscopic and structural description, the antibacterial properties of AgSFX were assayed using disc diffusion methods against Escherichia coli and Pseudomonas aeruginosa (Gram-negative), and Staphylococcus aureus (Gram-positive) bacterial strains. The AgSFX complex showed to be active against Gram-positive and Gram-negative bacterial strains, being comparable to the activities of silver sulfadiazine.

  16. A theobromine derived silver N-heterocyclic carbene: synthesis, characterization, and antimicrobial efficacy studies on cystic fibrosis relevant pathogens†

    PubMed Central

    Panzner, Matthew J.; Hindi, Khadijah M.; Wright, Brian D.; Taylor, Jane B.; Han, Daniel S.

    2009-01-01

    The increasing incidence of multidrug-resistant (MDR) pulmonary infections in the cystic fibrosis (CF) population has prompted the investigation of innovative silver based therapeutics. The functionalization of the naturally occurring xanthine theobromine at the N1 nitrogen atom with an ethanol substituent followed by the methylation of the N9 nitrogen atom gives the N-heterocyclic carbene precursor 1-(2-hydroxyethyl)-3,7,9-trimethylxanthinium iodide. The reaction of this xanthinium salt with silver acetate produces the highly hydrophilic silver carbene complex SCC8. The in vitro antimicrobial efficacy of this newly synthesized complex was evaluated with excellent results on a variety of virulent and MDR pathogens isolated from CF patients. A comparative in vivo study between the known caffeine derived silver carbene SCC1 and SCC8 demonstrated the ability of both complexes to improve the survival rates of mice in a pneumonia model utilizing the clinically isolated infectious strain of Pseudomonas aeruginosa PA M57-15. PMID:20449175

  17. Characterization of silver-kaolinite (AgK): an adsorbent for long-lived (129)I species.

    PubMed

    Sadasivam, Sivachidambaram; Rao, Sudhakar M

    2016-01-01

    Bentonite is a preferred buffer and backfill material for deep geological disposal of high-level nuclear waste (HLW). Bentonite does not retain anions by virtue of its negatively charged basal surface. Imparting anion retention ability to bentonite is important to enable the expansive clay to retain long-lived (129)I (iodine-129; half-life = 16 million years) species that may escape from the HLW geological repository. Silver-kaolinite (AgK) material is prepared as an additive to improve the iodide retention capacity of bentonite. The AgK is prepared by heating kaolinite-silver nitrate mix at 400 °C to study the kaolinite influence on the transition metal ion when reacting at its dehydroxylation temperature. Thermo gravimetric-Evolved Gas Detection analysis, X-ray diffraction analysis, X-ray photo electron spectroscopy and electron probe micro analysis indicated that silver occurs as AgO/Ag2O surface coating on thermally reacting kaolinite with silver nitrate at 400 °C. PMID:27026839

  18. Chlorine-free pyrotechnics: copper(I) iodide as a "green" blue-light emitter.

    PubMed

    Klapötke, Thomas M; Rusan, Magdalena; Sabatini, Jesse J

    2014-09-01

    The generation of blue-light-emitting pyrotechnic formulations without the use of chlorine-containing compounds is reported. Suitable blue-light emission has been achieved through the generation of molecular emitting copper(I) iodide. The most optimal copper(I) iodide based blue-light-emitting formulation was found to have performances exceeding those of chlorine-containing compositions, and was found to be insensitive to various ignition stimuli. PMID:25044436

  19. 21 CFR 73.2500 - Silver.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ..., is a crystalline powder of high purity silver prepared by the reaction of silver nitrate with ferrous... certification. Certification of this color additive is not necessary for the protection of the public health...

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

    SciTech Connect

    Hermon, H.; James, R.B.; Cross, E.

    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.

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

    SciTech Connect

    Hermon, H.; James, R.B.; Lund, J.

    1998-12-31

    In this study the authors report on the results of the investigation of lead iodide material properties. The effectiveness of a zone refining purification method on the material purity is determined by ICP-MS and ICP-OES and correlated to the electrical and physical material properties. They show that this zone refining method is very efficient in removing impurities from lead iodide, and they 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 much 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.

  2. Mechanistic aspects of ingested chlorine dioxide on thyroid function: impact of oxidants on iodide metabolism

    SciTech Connect

    Bercz, J.P.; Jones, L.L.; Harrington, R.M.; Bawa, R.; Condie, L.

    1986-11-01

    Toxicological studies dealing with recent findings of health effects of drinking water disinfectants are reviewed. Experiments with monkeys and rodents indicate that the biological activity of ingested disinfectants is expressed via their chemical interaction with the mucosal epithelia, secretory products, and nutritional contents of the alimentary tract. Evidence exists that a principal partner of this redox interaction is the iodide of nutritional origin that is ubiquitous in the gastrointestinal tract. Thus the observation that subchronic exposure to chlorine dioxide (ClO/sub 2/) in drinking water decreases serum thyroxine levels in mammalian species can be best explained with changes produced in the chemical form of the bioavailable iodide. Ongoing and previously reported mechanistic studies indicate that oxidizing agents such as chlorine-based disinfectants oxidize the basal iodide content of the gastrointestinal tract. The resulting reactive iodine species readily attaches to organic matter by covalent bonding. Evidence suggests that the extent to which such iodinated organics are formed is proportional to the magnitude of the electromotive force and stoichiometry of the redox couple between iodide and the disinfectant. Because the extent of thyroid uptake of the bioavailable iodide does not decrease during ClO/sub 2/ ingestion, it seems that ClO/sub 2/ does not cause iodide deficiency of sufficient magnitude to account for the decease in hormonogenesis. Absorption of one or more of iodinated molecules, e.g., nutrient, hormones, or cellular constituents of the alimentary tract having thyromimetic or thyroid inhibitory properties, is a better hypothesis for the effects seen.

  3. The effects and underlying mechanism of excessive iodide on excessive fluoride-induced thyroid cytotoxicity.

    PubMed

    Liu, Hongliang; Zeng, Qiang; Cui, Yushan; Yu, Linyu; Zhao, Liang; Hou, Changchun; Zhang, Shun; Zhang, Lei; Fu, Gang; Liu, Yeming; Jiang, Chunyang; Chen, Xuemin; Wang, Aiguo

    2014-07-01

    In many regions, excessive fluoride and excessive iodide coexist in groundwater, which may lead to biphasic hazards to human thyroid. To explore fluoride-induced thyroid cytotoxicity and the mechanism underlying the effects of excessive iodide on fluoride-induced cytotoxicity, a thyroid cell line (Nthy-ori 3-1) was exposed to excessive fluoride and/or excessive iodide. Cell viability, lactate dehydrogenase (LDH) leakage, reactive oxygen species (ROS) formation, apoptosis, and the expression levels of inositol-requiring enzyme 1 (IRE1) pathway-related molecules were detected. Fluoride and/or iodide decreased cell viability and increased LDH leakage and apoptosis. ROS, the expression levels of glucose-regulated protein 78 (GRP78), IRE1, C/EBP homologous protein (CHOP), and spliced X-box-binding protein-1 (sXBP-1) were enhanced by fluoride or the combination of the two elements. Collectively, excessive fluoride and excessive iodide have detrimental influences on human thyroid cells. Furthermore, an antagonistic interaction between fluoride and excessive iodide exists, and cytotoxicity may be related to IRE1 pathway-induced apoptosis. PMID:25104093

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

    NASA Astrophysics Data System (ADS)

    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.

  5. A novel mechanism of sodium iodide symporter repression in differentiated thyroid cancer.

    PubMed

    Smith, Vicki E; Read, Martin L; Turnell, Andrew S; Watkins, Rachel J; Watkinson, John C; Lewy, Greg D; Fong, Jim C W; James, Sally R; Eggo, Margaret C; Boelaert, Kristien; Franklyn, Jayne A; McCabe, Christopher J

    2009-09-15

    Differentiated thyroid cancers and their metastases frequently exhibit reduced iodide uptake, impacting on the efficacy of radioiodine ablation therapy. PTTG binding factor (PBF) is a proto-oncogene implicated in the pathogenesis of thyroid cancer. We recently reported that PBF inhibits iodide uptake, and have now elucidated a mechanism by which PBF directly modulates sodium iodide symporter (NIS) activity in vitro. In subcellular localisation studies, PBF overexpression resulted in the redistribution of NIS from the plasma membrane into intracellular vesicles, where it colocalised with the tetraspanin CD63. Cell-surface biotinylation assays confirmed a reduction in plasma membrane NIS expression following PBF transfection compared with vector-only treatment. Coimmunoprecipitation and GST-pull-down experiments demonstrated a direct interaction between NIS and PBF, the functional consequence of which was assessed using iodide-uptake studies in rat thyroid FRTL-5 cells. PBF repressed iodide uptake, whereas three deletion mutants, which did not localise within intracellular vesicles, lost the ability to inhibit NIS activity. In summary, we present an entirely novel mechanism by which the proto-oncogene PBF binds NIS and alters its subcellular localisation, thereby regulating its ability to uptake iodide. Given that PBF is overexpressed in thyroid cancer, these findings have profound implications for thyroid cancer ablation using radioiodine. PMID:19706688

  6. New silver(I) coordination polymers constructed from pyrazine derivatives and aromatic carboxylic acids: Syntheses, structures and photoluminescence

    NASA Astrophysics Data System (ADS)

    Zhang, Ting; Huang, Hua-Qi; Mei, Hong-Xin; Wang, Dan-Feng; Wang, Xiao-Xiang; Huang, Rong-Bin; Zheng, Lan-Sun

    2015-11-01

    Five one-dimensional to three-dimensional coordination polymers have been synthesized by 2-chlorobenzoic acid (HL1), 2-nitrobenzoic acid (HL2), o-toluic acid (HL3), 2,3,5-trimethylpyrazine (tpyz) and 2,3,5,6-tetramethylpyrazine (mpyz) in the presence of NH3·H2O in mixed solvents systems, namely, {Ag4(tpyz)2(L1)4}n (1), {Ag2(tpyz) (L2)2}n (2), {Ag2(tpyz) (L3)2}n (3), {Ag2(mpyz) (L1)2}n (4), {Ag(mpyz) (L2) (H2O)}n (5). All the complexes have been characterized by elemental analyses, IR spectra and X-ray diffraction. Compound 1 shows a 3D framework. The tpyz ligand links 1D chain which was connected by silver atom and L1 anion into 3D framework. Compounds 2 and 4 possess a similar 2D network with (4, 4) topology. Complex 3 also exhibits a two-dimensional structure. There is a 1D silver chain in 3, which is the main difference from 2 and 4. So, 3 shows three-connected (4 8, 3) topology. For 5, only one oxygen of L2 coordinated to Ag(I) ions. The L2 anions were arranged in both sides of the chain, which was connected by silver atoms and mpyz ligands. Then, the uncoordinated carboxylate oxygen with coordinated water 1molecule oxygen through the hydrogen bond made the resultant structure to a 3D framework. Complexes 1-5 spanning from one-dimensional chains to three-dimensional framework suggest that carboxylates and the kinds of pyrazine derivatives play significant roles in the formation of such coordination architectures. The photoluminescence and thermogravimetric analysis (TGA) of the complexes were also investigated.

  7. The surface chemistry of vinyl iodide on Pt(111)

    SciTech Connect

    Liu, Z.M.; Zhou, X.L.; Buchanan, D.A.

    1992-03-11

    Regardless of exposure, only submonolayer amounts of vinyl iodide (CH{sub 2}CHI) decompose, either during adsorption on Pt(111) at 100 K or during subsequent heating to 165 K. The remainder desorbs molecularly. The dissociation products are vinyl (CH{sub 2}CH) fragments, an important C{sub 2} intermediate in hydrocarbon catalysis, and atomic iodine. Using the tools of surface science the authors have explored the formation and subsequent reactions of vinyl species in the presence of unavoidable coadsorbed atomic iodine. While some vinyl exists up to 450 K, there are two important and competitive lower temperature reaction channels which lead to ethylidyne (CCH{sub 3}) and ethylene (CH{sub 2}CH{sub 2}). From these results, the authors conclude that the rate of ethylidyne formation from adsorbed ethylene is controlled by the rate at which the first C-H bond in ethylene breaks, and in agreement with Zaera, the authors find that vinyl is a facile intermediate in the process. 28 refs., 12 figs., 3 tabs.

  8. Preparation and evaluation of mercuric iodide for crystal growth

    NASA Astrophysics Data System (ADS)

    Skinner, N. L.; Ortale, C.; Schieber, M. M.; van den Berg, L.

    1989-11-01

    Large quantities (on the order of several hundred kilograms) of consistent, high-quality mercuric iodide (HgI2) for crystal growth have not been commercially available. The hydrocarbon, anion and cation impurity levels varied considerably, occasionally preventing crystal growth. This occurred even though the starting material was from the same vendor and was subjected to the same purification treatment. This paper will describe an aqueous precipitation process of HgI2 preparation in batches of 3 kg using Hg(NO3)2, or HgCl2 and KI. Since these salts are produced in much larger quantities than HgI2, more consistent quality is available. The impurity content of these batches and single crystals grown from them have been evaluated. These results and those from several commercially available starting materials and their grown single crystals are compared. Some of the single crystals grown using the in-house prepared HgI2 have yielded a large number of spectroscopy-grade nuclear detectors. The influence of the major impurities will be discussed.

  9. Correlation between mercuric iodide detector performance and crystalline perfection

    NASA Astrophysics Data System (ADS)

    Schieber, M.; Ortale, C.; van den Berg, L.; Schnepple, W.; Keller, L.; Wagner, C. N. J.; Yelon, W.; Ross, F.; Georgeson, G.; Milstein, F.

    1989-11-01

    X-ray, neutron and gamma ray diffraction rocking curves; X-ray topography; microhardness; and optical microscopic measurements have been performed directly on several mercuric iodide (Hgl2) nuclear radiation detectors fabricated from single crystals grown from the vapor phase. Two types of detectors were measured: spectrometer types (grades A and B), which had resolutions of 5-10% for the 662 keV photopeak of 137Cs, or radiation counters (grades C and D), where the spectral resolution ranged from 11% to no resolution. A good correlation has been found between the detector grade and the full width at half maximum (FWHM) of both the X- and gamma ray rocking curves (i.e., the higher the detector grade (A or B), the narrower the FWHM of the diffraction peak). X-ray topography also correlated with well both the FWHM of the diffraction X-ray rocking curve and the detector grade. The uniformity of the microhardness of the HgI2 detectors was found to be proportional to the nuclear performance of the detector. The better spectrometer-grade detectors were softer and much more uniform in microhardness than the most inferior detectors. The better detectors were also found to have much smoother surfaces than the poorer detectors, as observed by optical microscopy studies.

  10. Polarization Effects in Methylammonium Lead Iodide Electronic Devices

    NASA Astrophysics Data System (ADS)

    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.

  11. Polycrystalline Mercuric Iodide Films on CMOS Readout Arrays

    PubMed Central

    Hartsough, Neal E.; Iwanczyk, Jan S.; Nygard, Einar; Malakhov, Nail; Barber, William C.; Gandhi, Thulasidharan

    2009-01-01

    We have created high-resolution x-ray imaging devices using polycrystalline mercuric iodide (HgI2) films grown directly onto CMOS readout chips using a thermal vapor transport process. Images from prototype 400×400 pixel HgI2-coated CMOS readout chips are presented, where the pixel grid is 30 μm × 30 μm. The devices exhibited sensitivity of 6.2 μC/Rcm2 with corresponding dark current of ∼2.7 nA/cm2, and a 80 μm FWHM planar image response to a 50 μm slit aperture. X-ray CT images demonstrate a point spread function sufficient to obtain a 50 μm spatial resolution in reconstructed CT images at a substantially reduced dose compared to phosphor-coated readouts. The use of CMOS technology allows for small pixels (30 μm), fast readout speeds (8 fps for a 3200×3200 pixel array), and future design flexibility due to the use of well-developed fabrication processes. PMID:20161098

  12. Structural Effects on the Bandstructure of Methylammonium Lead Iodide

    NASA Astrophysics Data System (ADS)

    Bernardi, Marco; Barker, Bradford A.; Vigil-Fowler, Derek; Neaton, Jeffrey B.; Louie, Steven G.; Louie Team

    Metal-organic halide perovskites possess peculiar physical properties. The carrier diffusion length in methylammonium lead iodide (MAPbI) exceeds 1 μm, but this unusually high value for a solution-processed material is poorly understood. We developed first-principles calculations of carrier lifetimes and diffusion lengths in semiconductors, which require accurate knowledge of the bandstructure. In this talk, we show that in MAPbI the structure strongly affects the bandstructure and band edges, and that density functional theory (DFT) is unable to predict the room temperature tetragonal structure due to the polymorphism of MAPbI. The Rashba splitting induced by the spin-orbit interaction, and the DFT band gap and effective masses, all depend strongly on the chosen structure, a point that previous work failed to address. Working with multiple stochastic realizations of large unit cells with random methylammonium orientations, we compute average effective masses and show that the effective mass depends linearly on the band gap. The average Rashba coefficient we find is an order of magnitude smaller than previously reported, and the band edges are almost parabolic. Our structures possess the correct symmetry and are free of the spurious Pb off-centering assumed in previous work. We identify the correct starting point for GW bandstructure calculations and to compute the carrier lifetime and diffusion length.

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

    PubMed Central

    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-effect transistors. Field-effect carrier mobility is found to increase by almost two orders of magnitude below 200 K, consistent with phonon scattering-limited transport. Under balanced ambipolar carrier injection, gate-dependent electroluminescence is also observed from the transistor channel, with spectra revealing the tetragonal to orthorhombic phase transition. This demonstration of CH3NH3PbI3 light-emitting field-effect transistors provides intrinsic transport parameters to guide materials and solar cell optimization, and will drive the development of new electro-optic device concepts, such as gated light-emitting diodes and lasers operating at room temperature. PMID:26108967

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

    PubMed

    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-effect transistors. Field-effect carrier mobility is found to increase by almost two orders of magnitude below 200 K, consistent with phonon scattering-limited transport. Under balanced ambipolar carrier injection, gate-dependent electroluminescence is also observed from the transistor channel, with spectra revealing the tetragonal to orthorhombic phase transition. This demonstration of CH3NH3PbI3 light-emitting field-effect transistors provides intrinsic transport parameters to guide materials and solar cell optimization, and will drive the development of new electro-optic device concepts, such as gated light-emitting diodes and lasers operating at room temperature. PMID:26108967

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

    NASA Astrophysics Data System (ADS)

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

    2015-06-01

    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-effect transistors. Field-effect carrier mobility is found to increase by almost two orders of magnitude below 200 K, consistent with phonon scattering-limited transport. Under balanced ambipolar carrier injection, gate-dependent electroluminescence is also observed from the transistor channel, with spectra revealing the tetragonal to orthorhombic phase transition. This demonstration of CH3NH3PbI3 light-emitting field-effect transistors provides intrinsic transport parameters to guide materials and solar cell optimization, and will drive the development of new electro-optic device concepts, such as gated light-emitting diodes and lasers operating at room temperature.

  16. Chloride, bromide and iodide scintillators with europium doping

    DOEpatents

    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.

  17. Dissociative photodetachment dynamics of the iodide-aniline cluster

    NASA Astrophysics Data System (ADS)

    Bowen, M. Shane; Becucci, Maurizio; Continetti, Robert E.

    2006-10-01

    The photodetachment dynamics of the iodide-aniline cluster, I-(C6H5NH2), were investigated using photoelectron-photofragment coincidence spectroscopy at several photon energies between 3.60 and 4.82eV in concert with density functional theory calculations. Direct photodetachment from the solvated I- chromophore and a wavelength-independent autodetachment process were observed. Autodetachment is attributed to a charge-transfer-to-solvent reaction in which incipient continuum electrons photodetached from I- are temporarily captured by the nascent neutral iodine-aniline cluster configured in the anion geometry. Subsequent dissociation of the neutral cluster removes the stabilization, leading to autodetachment of the excess electron. The dependence of the dissociative photodetachment (DPD) and autodetachment dynamics on the final spin-orbit electronic state of the iodine fragment is characterized. The dissociation dynamics of the neutral fragments correlated with autodetached electrons were found to be identical to the DPD dynamics of the I atom product spin-orbit state closest to threshold at a given photon energy, lending support to the proposed sequential mechanism.

  18. Detection of the oxygen consumption rate of migrating zebrafish by electrochemical equalization systems.

    PubMed

    Yasukawa, Tomoyuki; Koide, Masahiro; Tatarazako, Norihisa; Abe, Ryoko; Shiku, Hitoshi; Mizutani, Fumio; Matsue, Tomokazu

    2014-01-01

    A novel measurement system to determine oxygen consumption rates via respiration in migrating Zebrafish (Danio rerio) has been developed. A signal equalization system was adapted to detect oxygen in a chamber with one fish, because typical electrochemical techniques cannot measure respiration activities for migrating organisms. A closed chamber was fabricated using a pipet tip attached to a Pt electrode, and a columnar Vycor glass tip was used as the salt bridge. Pt electrode, which was attached to the chamber with one zebrafish, and Ag electrode were immersed in 10 mM potassium iodide (KI), and both the electrodes were connected externally to form a galvanic cell. Pt and Ag electrodes act as the cathode and anode to reduce oxygen and oxidize silver, respectively, allowing the deposition of insoluble silver iodide (AgI). The AgI acts as the signal source accumulated on the Ag electrode by conversion of oxygen. The amount of AgI deposited on the Ag electrode was determined by cathodic stripping voltammetry. The presence of zebrafish or its embryo led to a decrease in the stripping currents generated by a 10 min conversion of oxygen to AgI. The conversion of oxygen to AgI is disturbed by the migration of the zebrafish and allows the detection of different equalized signals corresponding to respiration activity. The oxygen consumption rates of the zebrafish and its embryo were estimated and determined to be ∼4.1 and 2.4 pmol·s(-1), respectively. The deposited AgI almost completely disappeared with a single stripping process. The signal equalization system provides a method to determine the respiration activities for migrating zebrafish and could be used to estimate environmental risk and for effective drug screening. PMID:24328209

  19. 21 CFR 73.2500 - Silver.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 1 2011-04-01 2011-04-01 false Silver. 73.2500 Section 73.2500 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES GENERAL LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2500 Silver. (a) Identity. (1) The color additive, silver, is a crystalline powder of high purity...

  20. Fluorescent silver nanoclusters stabilized by DNA scaffolds.

    PubMed

    Yuan, Zhiqin; Chen, Ying-Chieh; Li, Hung-Wen; Chang, Huan-Tsung

    2014-09-01

    Fluorescent silver nanoclusters, in particular DNA stabilized (templated) silver nanoclusters, have attracted much attention because of their molecule-like optical properties, strong fluorescence and good biocompatibility. In this feature article, we summarize the DNA stabilized silver nanoclusters from the viewpoints of synthesis, optical properties, as well as recent applications in biological detection and imaging. PMID:24901353

  1. The Myth of the Silver Surfer

    ERIC Educational Resources Information Center

    Gorard, Stephen; Selwyn, Neil

    2008-01-01

    In this article, the authors write about the myth of the "silver surfers"--those third-age learners adept at using the internet and other technologies for a mixture of formal and informal learning episodes. The notion of the silver surfer has endured since the latter half of the 1990s. It is sustained by the annual Silver Surfer week, media…

  2. Geometrical parameters effects on local electric field enhancement of silver-dielectric-silver multilayer nanoshell

    SciTech Connect

    Shirzaditabar, Farzad; Saliminasab, Maryam

    2013-05-15

    The local electric field enhancement at different points of silver-dielectric-silver nanoshell is investigated using quasi-static theory. Because of the symmetric and anti-symmetric coupling between surface plasmon of inner silver core and outer silver shell, the local electric field spectrum of silver-dielectric-silver has two distinct peaks at resonance wavelengths. The silver core size and middle dielectric thickness affect the local electric field enhancement at different points of silver-dielectric-silver nanoshell. Increasing the silver core radius always leads to blue shift of shorter resonance wavelength and red shift of longer resonance wavelength. We observed two distinct local electric field peaks, which are corresponded to the symmetric and anti-symmetric coupling between inner and outer surface plasmons. In a system with thick silver shell, local electric field enhancement is greater than a system with thin silver shell. However, the local electric field variations as a function of silver core radius in both systems are different at different points of nanoshell. The effects of the dielectric thickness variations on local electric field are different from those from silver core size variations. As the dielectric thickness is about 3 nm, the highest local electric field enhancement occurs at the surface of the inner silver core, where the symmetric and anti-symmetric modes are mixed together.

  3. Geometrical parameters effects on local electric field enhancement of silver-dielectric-silver multilayer nanoshell

    NASA Astrophysics Data System (ADS)

    Shirzaditabar, Farzad; Saliminasab, Maryam

    2013-05-01

    The local electric field enhancement at different points of silver-dielectric-silver nanoshell is investigated using quasi-static theory. Because of the symmetric and anti-symmetric coupling between surface plasmon of inner silver core and outer silver shell, the local electric field spectrum of silver-dielectric-silver has two distinct peaks at resonance wavelengths. The silver core size and middle dielectric thickness affect the local electric field enhancement at different points of silver-dielectric-silver nanoshell. Increasing the silver core radius always leads to blue shift of shorter resonance wavelength and red shift of longer resonance wavelength. We observed two distinct local electric field peaks, which are corresponded to the symmetric and anti-symmetric coupling between inner and outer surface plasmons. In a system with thick silver shell, local electric field enhancement is greater than a system with thin silver shell. However, the local electric field variations as a function of silver core radius in both systems are different at different points of nanoshell. The effects of the dielectric thickness variations on local electric field are different from those from silver core size variations. As the dielectric thickness is about 3 nm, the highest local electric field enhancement occurs at the surface of the inner silver core, where the symmetric and anti-symmetric modes are mixed together.

  4. Durable silver coating for mirrors

    DOEpatents

    Wolfe, Jesse D.; Thomas, Norman L.

    2000-01-01

    A durable multilayer mirror includes reflective layers of aluminum and silver and has high reflectance over a broad spectral range from ultraviolet to visible to infrared. An adhesion layer of a nickel and/or chromium alloy or nitride is deposited on an aluminum surface, and a thin layer of silver is then deposited on the adhesion layer. The silver layer is protected by a passivation layer of a nickel and/or chromium alloy or nitride and by one or more durability layers made of metal oxides and typically a first layer of metal nitride. The durability layers may include a composite silicon aluminum nitride and an oxinitride transition layer to improve bonding between nitride and oxide layers.

  5. Sulfidation of silver nanoparticles

    NASA Astrophysics Data System (ADS)

    Levard, C.; Michel, F. M.; Brown, G. E.

    2010-12-01

    Rapid development of nanotechnologies that exploit the properties of silver nanoparticles (Ag-NPs) raises questions concerning the impact of Ag on the environment. Ag-NPs are currently among the most widely used in the nanotechnology industry and the amount released into the environment is expected to increase along with production (1). When present in geochemical systems, Ag-NPs may undergo a variety of changes due to varying redox, pH, and chemical conditions. Expected changes range from surface modification (e.g., oxidation, sulfidation, chloridation etc.) to complete dissolution and re-precipitation. In this context, the focus of our work is on understanding the behavior of synthetic Ag-NPs with different particle sizes under varying conditions relevant to the environment. Sulfidation of Ag-NPs is of particular interest since it among the processes most likely to occur in aqueous systems, in particular under reducing conditions. Three sizes of Ag-NPs coated with polyvinyl pyrrolidone were produced using the polyol process (2) (7 ±1; 20 ±4, and 40 ±9 nm). Batch solutions containing the different Ag-NPs were subsequently reacted with Na2S solutions of different concentrations. The sulfidation process was followed step-wise for 24 hours and the corrosion products formed were characterized by electron microscopy (TEM/SEM), diffraction (XRD), and photo-electron spectroscopy (XPS). Surface charge (pHPZC) of the products formed during this process was also measured, as were changes in solubility and reactivity. Based on experimental observations we infer that the sulfidation process is the result of dissolution-precipitation and find that: (i) acanthite (Ag2S) is formed as a corrosion product; (ii) Ag-NPs aggregation increased with sulfidation rate; (iii) pHPZC increases with the rate of sulfidation; and (iv) the solubility of the corrosion products formed from sulfidation appears lower than that of non-sulfidated Ag-NPs. We observe size-dependent differences in

  6. Auto-ionization in lutetium iodide complexes: effect of the Iioic radius on lanthanide-iodide binding.

    PubMed

    Giesbrecht, Garth R; Gordon, John C; Clark, David L; Scott, Brian L

    2004-02-01

    Reaction of lutetium metal with 1.5 equiv of elemental iodine in 2-propanol leads to the isolation of LuI(3)(HO(i)Pr)(4) (1). An X-ray crystal structure reveals an ionic structure with well-separated [LuI(2)(HO(i)Pr)(4)] cations and [I] anions. Dissolution of 1 in pyridine generates the unusual alkoxide species [LuI(O(i)Pr)(py)(5)][I] (2) with the elimination of HI. An X-ray crystal structure of 2 confirmed the ionic nature of the compound, with the cationic portion of the complex exhibiting a seven-coordinated lutetium center with trans-disposed iodo and alkoxide ligands and five pyridine molecules equally displaced within the equatorial plane. Exposure of 2 to iodotrimethylsilane yields the expected triiodide species [LuI(2)(py)(5)][I] (3), which may also be prepared by refluxing commercially available LuI(3) in THF, followed by crystallization from a THF/pyridine mixture. The solid-state structure of 3 is similar to that of 2, with the alkoxide ligand having been replaced by an iodide. The formation of ionic structures 1-3 as opposed to the higher-coordinated neutral species may be traced to the small lutetium center and the presence of relatively strong Lewis bases within the coordination sphere of the metal. PMID:14753829

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

    PubMed

    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

  8. Amination of aryl halides with aqueous ammonia catalyzed by green recyclable poly(4-vinylpyridine)-supported copper iodide nanoparticles catalyst.

    PubMed

    Albadi, Jalal; Shiran, Jafar Abbasi; Mansournezhad, Azam

    2014-01-01

    In this research efficient procedure for the amination of aryl halides with aqueous ammonia in the presence of poly(4-vinylpyridine)-supported copper iodide nanoparticles catalyst is reported. A wide range of aryl halides including aryl iodides and aryl bromides are converted into the corresponding aniline derivatives. The experimental procedure with poly(4-vinylpyridine)-supported copper iodide nanoparticles catalyst is quite straightforward and it is recycled up to 3 consecutive runs by simple filtration. PMID:25551733

  9. Iodide Residues in Milk Vary between Iodine-Based Teat Disinfectants.

    PubMed

    French, Elizabeth A; Mukai, Motoko; Zurakowski, Michael; Rauch, Bradley; Gioia, Gloria; Hillebrandt, Joseph R; Henderson, Mark; Schukken, Ynte H; Hemling, Thomas C

    2016-07-01

    Majority of iodine found in dairy milk comes from the diet and teat disinfection products used during milking process. The objective of this study was to evaluate the effects of 4 iodine-based teat dips on milk iodide concentrations varying in iodine level (0.25% vs. 0.5%, w/w), normal low viscosity dip versus barrier dip, and application method (dip vs. spray) to ensure safe iodine levels in dairy milk when these products are used. The iodine exposure study was performed during a 2-wk period. The trial farm was purged of all iodine-based disinfection products for 21 d during a prestudy "washout period," which resulted in baseline milk iodide range of 145 to 182 ppb. During the experiment, iodine-based teat dips were used as post-milking teat disinfectants and compared to a non-iodine control disinfectant. Milk iodide residue levels for each treatment was evaluated from composited group samples. Introduction of different iodine-based teat disinfectants increased iodide residue content in milk relative to the control by between 8 and 29 μg/L when averaged across the full trial period. However, residues levels for any treatment remained well below the consumable limit of 500 μg/L. The 0.5% iodine disinfectant increased milk iodide levels by 20 μg/L more compared to the 0.25% iodine. Compared to dip-cup application, spray application significantly increased milk iodide residue by 21 μg/L and utilized approximately 23% more teat dip. This carefully controlled study demonstrated an increase in milk iodide concentrations from iodine disinfectants, but increases were small and within acceptable limits. PMID:27259164

  10. In vitro study of acute toxic effects of high iodide doses in human thyroid follicles.

    PubMed

    Many, M C; Mestdagh, C; van den Hove, M F; Denef, J F

    1992-08-01

    The acute effects of increasing doses of sodium iodide were studied on human thyroid follicles isolated from normal paranodular tissue. After 24 h incubation in culture medium, follicles isolated from most thyroids maintained their capacity for 125I accumulation and organification and a normal cellular ultrastructure. 125I accumulation was significantly increased after addition of TSH, whereas 125I organification was not affected. In presence of TSH, numerous follicles had large empty-looking follicular lumina unlabeled on autoradiographies. Follicles incubated for 24 h in the presence of a low concentration (10(-7) M) of iodide retained their function and morphology. However, incubation with a high dose of iodide (10(-3) M) caused marked inhibition of 125I accumulation and organification reaching values similar to those obtained in presence of inhibitors of iodide trapping and organification. At high doses, iodide induced necrosis of thyroid epithelial cells: the percentage of necrotic cells was significantly increased with 10(-5) M and doubled with 10(-3) M as compared to values measured at 10(-7) M. Ultrastructural lesions such as apical blebbing, cytoplasmic fragments desquamation, endoplasmic reticulum vesiculation, and accumulation of lipofuscin in secondary lysosomes were also present. The necrotic effect and the ultrastructural alterations also occurred in the presence of TSH but were prevented by the addition of inhibitors of iodide trapping or organification. These results demonstrate a direct acute toxic effect of iodide in human thyroid cells. The nature of the ultrastructural alterations is in agreement with a mechanism of toxicity involving a free radical attack and lipid peroxidation as observed in other tissues. PMID:1639011

  11. Ozonation of iodide-containing waters: selective oxidation of iodide to iodate with simultaneous minimization of bromate and I-THMs.

    PubMed

    Allard, S; Nottle, C E; Chan, A; Joll, C; von Gunten, U

    2013-04-15

    The presence of iodinated disinfection by-products (I-DBPs) in drinking water poses a potential health concern since it has been shown that I-DBPs are generally more genotoxic and cytotoxic than their chlorinated and brominated analogs. I-DBPs are formed during oxidation/disinfection of iodide-containing waters by reaction of the transient hypoiodous acid (HOI) with natural organic matter (NOM). In this study, we demonstrate that ozone pre-treatment selectively oxidizes iodide to iodate and avoids the formation of I-DBPs. Iodate is non-toxic and is therefore a desired sink of iodine in drinking water. Complete conversion of iodide to iodate while minimizing the bromate formation to below the guideline value of 10 μg L⁻¹ was achieved for a wide range of ozone doses in five raw waters with DOC and bromide concentrations of 1.1-20 mg L⁻¹ and 170-940 μg L⁻¹, respectively. Lowering the pH effectively further reduced bromate formation but had no impact on the extent of iodate and bromoform formation (the main trihalomethane (THM) formed during ozonation). Experiments carried out with pre-chlorinated/post-clarified samples already containing I-DBPs, showed that ozonation effectively oxidized I-THMs. Therefore, in iodide-containing waters, in which I-DBPs can be produced upon chlorination or especially chloramination, a pre-ozonation step to oxidize iodide to iodate is an efficient process to mitigate I-DBP formation. PMID:23351431

  12. Effect of Excessive Potassium Iodide on Rat Aorta Endothelial Cells.

    PubMed

    Zhang, Man; Zou, Xiaoyan; Lin, Xinying; Bian, Jianchao; Meng, Huicui; Liu, Dan

    2015-08-01

    The aim of the current study was to investigate the effect of excess iodine on rat aorta endothelial cells and the potential underlying mechanisms. Rat aorta endothelial cells were cultured with iodide ion (3506, 4076, 4647, 5218, 5789, 6360, 6931, and 7512 mg/L) for 48 h. Morphological changes of cells were observed with microscope after Wright-Giemsa staining and acridine orange staining. Cell proliferation was determined with 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay, and cell apoptosis was assessed with flow cytometry. The activity of superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), endothelial nitric oxide synthase (eNOS), induced nitric oxide synthase (iNOS), and concentrations of malondialdehyde (MDA), glutathione (GSH), and protein carbonyl in culture medium were determined with colorimetric method. The expression of intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) was detected by enzyme linked immunosorbent assay. The results showed that excess iodine induced abnormal morphologic changes of cells, inhibited cell proliferation, and increased apoptosis rate. Iodine also reduced the activity of SOD, GSH-Px, and concentrations of GSH and increased the concentrations of MDA and protein carbonyl in a dose-dependent manner. Moreover, excess iodine decreased the activity of eNOS and increased the activity of iNOS and the expression of ICAM-1 and VCAM-1 in culture medium. Our results suggested that excess iodine exposure increased oxidative stress, caused damage of vascular endothelial cells, and altered the expression of adhesion factors and the activity of NOS. These changes may explain the mechanisms underlying excess iodine-induced vascular injury. PMID:25690517

  13. Characterization of strontium iodide scintillators with silicon photomultipliers

    NASA Astrophysics Data System (ADS)

    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.

  14. Degradation of methyl iodide in soil: effects of environmental factors.

    PubMed

    Guo, Mingxin; Gao, Suduan

    2009-01-01

    Methyl iodide (MeI) is a promising alternative to the phased-out fumigant methyl bromide (MeBr); however, there are concerns about its environmental fate following soil fumigation. Laboratory experiments were conducted to investigate the effect of various environmental factors on the rate of MeI degradation in soil. The chemical was added to soil at 48.6 mg kg(-1) and incubated under different conditions. The MeI degradation rate in soil was determined by extracting and measuring residual concentrations over a 15 d incubation period. In soil, MeI degradation followed availability-adjusted first-order kinetics. At 20 degrees C MeI had a calculated half-life of 32 d in a sandy loam containing 4.3 g kg(-1) of organic carbon. It degraded more rapidly as temperature increased, exhibiting a half-life of 23 d at 30 degrees C. Amendment with 10% cattle manure shortened the half-life to 4 d at 20 degrees C. In both unamended and manure-amended soils, the half-life of MeI greatly increased as the organic matter (OM) was removed and it only slightly increased in soils that were sterilized, indicating predominance of chemical reactions in MeI degradation. Soil texture, mineralogy, and moderate moisture content had little influence on MeI degradation. The degradation slowed as the chemical application rate increased. The results suggest that environmental factors, especially soil temperature and organic amendments, should be considered in combination with the minimum effective MeI application rate for achieving satisfactory pest-control efficacy, reducing atmospheric volatilization, and minimizing groundwater contamination. PMID:19202021

  15. Cytotoxicity of silver dressings on diabetic fibroblasts.

    PubMed

    Zou, Shi-Bo; Yoon, Won-Young; Han, Seung-Kyu; Jeong, Seong-Ho; Cui, Zheng-Jun; Kim, Woo-Kyung

    2013-06-01

    A large number of silver-based dressings are commonly used in the management of chronic wounds that are at risk of infection, including diabetic foot ulcers. However, there are still controversies regarding the toxicity of silver dressings on wound healing. The purpose of this study was to objectively test the cytotoxicity of silver dressings on human diabetic fibroblasts. Human diabetic fibroblasts were obtained from the foot skin of four diabetic foot ulcer patients and cultured. The effect of five silver-containing dressing products (Aquacel Ag, Acticoat*Absorbent, Medifoam Ag, Biatain Ag and PolyMem Ag) and their comparable silver-free dressing products on morphology, proliferation and collagen synthesis of the cultured human diabetic fibroblasts were compared in vitro. In addition, extracts of each dressing were tested in order to examine the effect of other chemical components found in the dressings on cytotoxicity. The diabetic fibroblasts cultured with each silver-free dressing adopted the typical dendritic and fusiform shape. On the other hand, the diabetic fibroblasts did not adopt this typical morphology when treated with the different silver dressings. All silver dressings tested in the study reduced the viability of the diabetic fibroblasts and collagen synthesis by 54-70 and 48-68%, respectively, when compared to silver-free dressings. Silver dressings significantly changed the cell morphology and decreased cell proliferation and collagen synthesis of diabetic fibroblasts. Therefore, silver dressings should be used with caution when treating diabetic wounds. PMID:22533495

  16. Influence of injected silver content on synthesis of silver coated nickel particles by DC thermal plasma

    NASA Astrophysics Data System (ADS)

    Park, Si Taek; Kim, Tae-Hee; Park, Dong-Wha

    2016-06-01

    Silver nanoparticle-coated spherical nickel particles were prepared from a mixture of micro-sized silver and nickel as raw materials by DC thermal plasma treatment. The mixture of micro-sized silver and nickel powders was injected into the high-temperature region of an argon thermal plasma jet. Although the silver, with its very high thermal conductivity and relatively low boiling point, was thoroughly evaporated by this process, nickel was not evaporated perfectly because of its comparatively low thermal conductivity and high boiling point. The rough nickel powder was spheroidized as it melted. Finally, silver evaporated by the thermal plasma quickly condensed into nanoparticles on the surfaces of the micro-sized spherical nickel particles, aided by the sharp temperature gradient of the thermal plasma jet. With varying the ratios of silver to nickel feedstock from 1:10 to 5:1, the products synthesized in each condition were examined by XRD, XPS, FE-SEM, and FE-TEM. More silver nanoparticles were attached on the nickel by increasing the injected feedstock to 9.8 at% silver. Meanwhile, a decrease of silver in the products was observed when larger amounts of silver were introduced to the thermal plasma jet. The exposed silver components decreased with greater proportions of silver feedstock because of the metal's dendritic structure and the formation of silver-coated silver particles.

  17. Conditional pharmacology/toxicology V: ambivalent effects of thiocyanate upon the development and the inhibition of experimental arthritis in rats by aurothiomalate (Myocrysin®) and metallic silver.

    PubMed

    Whitehouse, Michael; Butters, Desley; Vernon-Roberts, Barrie

    2013-08-01

    This article discusses the bizarre and contrary effects of thiocyanate, the major detoxication product of hydrogen cyanide inhaled from tobacco smoke or liberated from cyanogenic foods, e.g. cassava. Thiocyanate both (1) promotes inflammatory disease in rats and (2) facilitates the anti-inflammatory action of historic metal therapies based on gold (Au) or silver (Ag) in three models of chronic polyarthritis in rats. Low doses of nanoparticulate metallic silver (NMS) preparations, i.e. zerovalent silver (Ag°) administered orally, suppressed the mycobacterial ('adjuvant')-induced arthritis (MIA) in rats. Similar doses of cationic silver, Ag(I), administered orally as silver oxide or soluble silver salts were inactive. By contrast, NMS only inhibited the development of the collagen-induced arthritis (CIA) and pristane-induced arthritis (PIA) in rats when thiocyanate was also co-administered in drinking water. These (a) arthritis-selective and (b) thiocyanate-inducible effects of Ag° were also observed in some previous, and now extended, studies with the classic anti-arthritic drug, sodium aurothiomalate (ATM, Myocrisin(®)) and its silver analogue (STM), administered subcutaneously to rats developing the same three forms of polyarthritis. In the absence of either Ag° or ATM, thiocyanate considerably increased the severity of the MIA, CIA and PIA, i.e. acting as a pro-pathogen. Hitherto, thiocyanate was considered relatively harmless. This may not be true in rats/people with immuno-inflammatory stress and concomitant leukocyte activation. Collectively, these findings show how the drug action of a xenobiotic might be determined by the nature (and severity) of the experimental inflammation, as an example of conditional pharmacology. They also suggest that an incipient toxicity, even of normobiotics such as thiocyanate, might likewise be modulated beneficially by well-chosen xenobiotics (drugs, nutritional supplements, etc.), i.e. conditional toxicology (Powanda 1995

  18. Spectroscopic studies, DFT calculations, and cytotoxic activity of novel silver(I) complexes of hydroxy ortho-substituted-nitro-2H-chromen-2-one ligands and a phenanthroline adduct.

    PubMed

    Mujahid, Muhammad; Kia, Agnieszka Foltyn-Arfa; Duff, Brian; Egan, Denise A; Devereux, Michael; McClean, Siobhán; Walsh, Maureen; Trendafilova, Natasha; Georgieva, Ivelina; Creaven, Bernadette S

    2015-12-01

    Silver(I) complexes of coumarin-based ligands and one of their phenanthroline (phen) adducts have been prepared and characterized using microanalytical data, molar conductivity, IR, (1)H and (13)C NMR, UV-Vis, and atomic absorption (AAS) spectroscopies. The binding modes of the coumarin-based ligands and the most probable structure of their Ag(I) complexes were predicted by means of molecular modeling and calculations of their IR, NMR, and absorption spectra using density functional theory (DFT). The cytotoxicity of the compounds studied against human-derived hepatic carcinoma cells (Hep-G2) and a renal cancer cell line (A498) showed that the complexes were more cytotoxic than the clinically used chemotherapeutic, mitoxantrone. The compounds showed little interaction with DNA and also did not show nuclease activity but manifested excellent superoxide dismutase activity which may indicate that their mechanism of action is quite different to many metal-based therapeutics. PMID:26492162

  19. Gold, Silver and Bronze Citations.

    ERIC Educational Resources Information Center

    American School & University, 2003

    2003-01-01

    Presents the gold, silver, and bronze winners of a competition, which judged the most outstanding learning environments at educational institutions nationwide. Jurors spent two days reviewing projects, focusing on concepts and ideas that made them exceptional. For each citation, the article offers information on the firm, client, total area, total…

  20. The green synthesis, characterization, and evaluation of the biological activities of silver nanoparticles synthesized from Leptadenia reticulata leaf extract

    NASA Astrophysics Data System (ADS)

    Kumara Swamy, M.; Sudipta, K. M.; Jayanta, K.; Balasubramanya, S.

    2015-01-01

    Biosynthesis of silver nanoparticles (Ag Nps) was carried out using methanol leaves extract of L. reticulata. Ag Nps were characterized based on the observations of UV-visible spectroscopy, transmission electron microscopy, and X-ray diffraction (XRD) analysis. These Ag Nps were tested for antimicrobial activity by agar well diffusion method against different pathogenic microorganisms and antioxidant activity was performed using DPPH assay. Further, the in vitro cytotoxic effects of Ag Nps were screened against HCT15 cancer cell line and viability of tumor cells was confirmed using MTT ((3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide, a yellow tetrazole)) assay. The nuclear condensation was studied using the propidium iodide-staining method. The color change from green to dark brown and the absorbance peak at about 420 nm indicated the formation of nanoparticles. XRD pattern showed characteristic peaks indexed to the crystalline planes (111), (200) and (220) of face-centered cubic silver. The nanoparticles were of spherical shape with varying sizes ranging from 50 to 70 nm. Biosynthesized Ag Nps showed potent antibacterial activity and effective radical scavenging activity. MTT assay revealed a dose-dependent decrease in cell viability. Microscopic observations showed distinct cellular morphological changes indicating unhealthy cells, whereas the control appeared normal. Increase in the number of propidium iodide positive cells were observed in maximum concentration. Methanolic leaf extract of L. reticulata acts as an excellent capping agent for the formation of silver nanoparticles and demonstrates immense biological activities. Hence, these Ag NPs can be used as antibacterial, antioxidant as well as cytotoxic agent in treating many medical complications.

  1. Plasmonic characterization of photo-induced silver nanoparticles extracted from silver halide based TEM film

    NASA Astrophysics Data System (ADS)

    Sudheer, Tiwari, P.; Varshney, G. K.; Rai, V. N.; Srivastava, A. K.

    2016-05-01

    The plasmonic responses of silver nanoparticles extracted from silver halide based electron microscope film are investigated. Photo-reduction process is carried out to convert the silver halide grains into the metallic silver. The centrifuge technique is used for separating the silver nanoparticles from the residual solution. Morphological study performed by field emission scanning electron microscope (FESEM) shows that all the nanoparticles have an average diameter of ~120 nm with a high degree of mono dispersion in size. The localized surface plasmon resonance (LSPR) absorption peak at ~537 nm confirms the presence of large size silver nanoparticles.

  2. Formation of iodinated organic compounds by oxidation of iodide-containing waters with manganese dioxide.

    PubMed

    Gallard, Hervé; Allard, Sébastien; Nicolau, Rudy; von Gunten, Urs; Croué, Jean Philippe

    2009-09-15

    This study shows that iodinated organic compounds can be produced when iodide-containing waters are in contact with manganese oxide birnessite (delta-MnO2) in the pH range of 5-7. In the absence of natural organic matter (NOM), iodide is oxidized to iodate that is also adsorbed onto delta-MnO2. In the presence of iodide and NOM, adsordable organic iodine compounds (AOI) are formed at pH < 7 because of the oxidation of iodide to iodine by delta-MnO2 and the reactions of iodine with NOM. In addition, iodoacetic acid and iodoform have been identified as specific iodinated byproducts. Formation of iodoform is not observed for high NOM/delta-MnO2 ratios due to inhibition of the catalytic effect of delta-MnO2 by NOM poisoning. Experiments with model compounds such as resorcinol and 3,5-heptanedione confirmed that the delta-MnO2/l(-) system is very effective for the formation of iodinated organic compounds. These results suggest that birnessite acts as a catalyst through the oxidation of iodide to iodine and the polarization of the iodine molecule, which then reacts with NOM moieties. Furthermore, our results indicate that during water treatment in the presence of manganese oxide, iodinated organic compounds may be formed, which may lead to taste and odor or toxicological problems. PMID:19806734

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

    SciTech Connect

    Nacapricha, D.; Taylor, C.

    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.

  4. A Combined Experimental and Molecular Dynamics Study of Iodide-Based Ionic Liquid and Water Mixtures.

    PubMed

    Nickerson, Stella D; Nofen, Elizabeth M; Chen, Haobo; Ngan, Miranda; Shindel, Benjamin; Yu, Hongyu; Dai, Lenore L

    2015-07-16

    Iodide-based ionic liquids have been widely employed as iodide sources in electrolytes for applications utilizing the triiodide/iodide redox couple. While adding a low-viscosity solvent such as water to ionic liquids can greatly enhance their usefulness, mixtures of highly viscous iodide-containing ILs with water have never been studied. This paper investigates, for the first time, mixtures of water and the ionic liquid 1-butyl-3-methylimidazolium iodide ([BMIM][I]) through a combined experimental and molecular dynamics study. The density, melting point, viscosity, and conductivity of these mixtures were measured by experiment. The composition region below 50% water by mole was found to differ dramatically from the region above 50% water, with trends in density and melting point differing before and after that point. Water was found to have a profound effect on viscosity and conductivity of the IL, and the effect of hydrogen bonding was discussed. Molecular dynamics simulations representing the same mixture compositions were performed. Molecular ordering was observed, as were changes in this ordering corresponding to water content. Molecular ordering was related to the experimentally measured mixture properties, providing a possible explanation for the two distinct composition regions identified by experiment. PMID:26090562

  5. Evaluation of Glaciogenic Cloud Seeding using Trace Chemistry

    NASA Astrophysics Data System (ADS)

    Fisher, J.; Benner, S. G.; Kunkel, M. L.; Blestrud, D.; Holbrook, V. P.; Parkinson, S.

    2015-12-01

    Glaciogenic cloud seeding is an important scientific technology for enhancing water resources across in the Western United States. Cloud seeding enriches orographic super cooled liquid water layers with plumes of ice nuclei, increasing the water yield of a storm event. Weather model assessments of cloud seeding estimate controlled releases of the ice nucleating agent, silver iodide (AgI), increases snow precipitation between 3-15% annually. However, efficacy of cloud seeding programs are difficult to assess using Weather Research and Forecasting (WRF) models alone. Therefore, this study validated the spatial and temporal distribution of AgI predicted by WRF models using ultra-trace snow chemistry data collected in the target area. Field methods utilized in this study are unique to previous trace chemical assessments of cloud seeding in two ways. First, nearly all snow samples were collected within 24 hours of deposition. Focusing on freshly deposited snow was more effective at constraining AgI plume timing and spatial extent with greater precision (via WRF, SNOTEL, and chemistry data). Second, this study employed geostatistics to describe AgI variability on the pit scale, site scale, and regional scale to optimize on the amount of samples to collect. The analysis revealed 4 columns of vials per snow pit and 1 snow pit per sampling site are optimal. Identifying the seeding signature at the regional scale was also successfully accomplished over a 40 mile sampling transect. All 6 sites had an identical AgI seeding signature despite drastic differences in of canopy cover, aspect, and distance from AgI source. The furthest sites from the AgI source were difficult to identify with Ag concentrations alone. Therefore, enrichment factors were essential to locating AgI influence at the most distal sites.

  6. Antimicrobial Properties of a Novel Silver-Silica Nanocomposite Material▿

    PubMed Central

    Egger, Salome; Lehmann, Rainer P.; Height, Murray J.; Loessner, Martin J.; Schuppler, Markus

    2009-01-01

    Nanotechnology enables development and production of novel silver-based composite materials. We used in vitro tests to demonstrate the antimicrobial activity of a silver-silica nanocomposite compared to the activities of conventional materials, such as silver nitrate and silver zeolite. A silver-silica-containing polystyrene material was manufactured and shown to possess strong antimicrobial properties. PMID:19270121

  7. Isomeric differentiation of polycyclic aromatic hydrocarbons using silver nitrate reactive desorption electrospray ionization mass spectrometry

    PubMed Central

    Eftekhari, Mohammad; Ismail, Ali I.; Zare, Richard N.

    2014-01-01

    RATIONALE Polycyclic aromatic hydrocarbons (PAHs) are nonpolar and difficult to detect by desorption electrospray ionization. We present a new detection method based on cationization with silver ions, which has the added advantage of being able to differentiate PAHs with the same mass but different structure. METHODS 9,10-Diphenylanthracene and triptycene, in addition to four different groups of PAH isomers: (1) anthracene and phenanthrene, (2) pyrene and fluoranthene, (3) benz[a]anthracene, benz[b]anthracene (tetracene), and chrysene (4) benzo[a]pyrene and benzo[k]fluoranthene, were deposited on a paper surface and bombarded with methanol droplets containing silver nitrate. The resulting microdroplets entered a quadruple mass spectrometer for mass analysis. RESULTS The mass spectrum shows [PAH]+, [Ag + OH + PAH]+, and [Ag(PAH)n]+ n (n = 1, 2) (and [PAH + O2]+ in the case of benz[b]anthracene) ions. PAHs having a bay structure, such as phenanthrene, showed a different tendency to interact with silver ions from those PAHs having a linear arrangement of the fused benzene rings, such as anthracene. The ratios of the [PAH]+ peak intensity to that of [Ag–PAH]+, [Ag + OH + PAH]+, [Ag(PAH)2]+, and [PAH + O2]+ were used to differentiate the PAH isomers sharing the same molecular formula with different structures. For isomeric mixtures the [PAH]+ to [Ag + OH + PAH]+ ratio was found to be the most useful parameter. The uncertainty in the mole fraction of an isomeric mixture was ±0.09, 0.13, ±0.25, and ±0.1 for phenanthrene-anthracene, fl benz[a] anthracene-chrysene, and benzo[a]pyrene-benzo[k]fluoranthene, respectively. CONCLUSIONS A simple method has been developed for the detection of PAHs in desorption electrospray ionization mass spectrometry based on Ag(I) cationization. The method showed a capability to differentiate PAHs isomers (having the same molecular mass) in isomeric mixture with an uncertainty in the mole fraction of about 0.1. At high inlet temperature

  8. Effect of nano silver and silver nitrate on seed yield of (Ocimum basilicum L.)

    PubMed Central

    2014-01-01

    Background The aim of this study was to evaluate the effect of nano silver and silver nitrate on yield of seed in basil plant. The study was carried out in a randomized block design with three replications. Results Four levels of either silver nitrate (0, 100, 200 and 300 ppm) or nano silver (0, 20, 40, and 60 ppm) were sprayed on basil plant at seed growth stage. The results showed that there was no significant difference between 100 ppm of silver nitrate and 60 ppm concentration of nano silver on the shoot silver concentration. However, increasing the concentration of silver nitrate from 100 to 300 ppm caused a decrease in seed yield. In contrast, a raise in the concentration of nano silver from 20 to 60 ppm has led to an improvement in the seed yield. Additionally, the lowest amount of seed yield was found with control plants. Conclusions Finally, with increasing level of silver nitrate, the polyphenol compound content was raised but the enhancing level of nano silver resulting in the reduction of these components. In conclusion, nano silver can be used instead of other compounds of silver. PMID:25383311

  9. Immunogold silver staining for light microscopy.

    PubMed

    Lackie, P M

    1996-07-01

    The immunogold silver staining method (IGSS) is widely used as a sensitive and specific immunohistochemical visualisation technique. IGSS involves the specific deposition of metallic silver at the site of immunogold labelling and provides a means of visualisation at low magnification by light or electron microscopy. Silver developers for IGSS rapidly deposit metallic silver only at the site of heavy metals, including gold and silver, because of their catalytic activity. The developing solution contains the silver ions and reducing agent necessary for this reaction. Using different silver salts as ion donors and by selecting an appropriate temperature and pH, visible amounts of silver can be deposited in a few minutes at the site of colloidal gold labelling while little non-specific background deposition occurs. Inclusion of protective colloids in the solution can also be used to control the reaction. Although studies of the chemical basis of silver deposition around unlabelled colloidal gold date back to 1939, immunogold enhancement by silver was established in 1983. The IGSS method evolved from the combination of disparate photographic, histochemical and immunogold techniques which have been effectively combined and optimised over the last 10 years to provide a visualisation system which is well suited to many immunohistochemical studies. PMID:8858363

  10. Contemporary anthropogenic silver cycle: a multilevel analysis.

    PubMed

    Johnson, Jeremiah; Jirikowic, Julie; Bertram, Marlen; van Beers, D; Gordon, R B; Henderson, Kathryn; Klee, R J; Lanzano, Ted; Lifset, R; Oetjen, Lucia; Graedel, T E

    2005-06-15

    Anthropogenic cycling of silver in 1997 is presented using three discrete governmental units: 64 countries encompassing what we believe to be over 90% of global silver flows, 9 world regions, and the entire planet. Using material flow analysis (MFA) techniques, the country level cycles are aggregated to produce the regional cycles, which are used to form a "best estimate" global cycle. Interesting findings include the following: (1) several silver-mining countries export ore and concentrate but also import silver-containing semiproducts and products; (2) the level of development for a country, as indicated by the gross domestic product, is a fair indicator of silver use, but several significant outliers exist; (3) the countries with the greatest mine production include Mexico, the United States, Peru, and China, whereas the United States, Japan, India, Germany, and Italy lead in the fabrication and manufacture of products; (4) North America and Europe's use of silver products exceed that of other regions on a per capita basis; (5) global silver discards, including tailings and separation waste, totaled approximately 57% of the silver mined; (6) approximately 57% of the silver entering waste management globally is recycled; and (7) the amount of silver entering landfills globally is comparable to the amount found in tailings. The results of this MFA lay the basis for further analysis, which in turn can offer insight into natural resource policy, the characterization of environmental impact, and better resource management. PMID:16047806

  11. A 2-pyridyl (py) attached phosphine imine [P(Npy)(NHpy)3] and an imido phosphinate ion [P(Npy)2)(NHpy)2]- in its Ag(I) complex.

    PubMed

    Gupta, Arvind K; Chipem, Francis A S; Boomishankar, Ramamoorthy

    2012-02-14

    A new phosphine imine 3, [P(Npy)(NHpy)(3)] (py = 2-pyridyl), was synthesized from the phosphonium salt 1, [P(NHpy)(4)]Cl. Subsequent reaction of 1 or 3 with AgClO(4) lead to an unprecedented penta-nuclear Ag(I) complex 4 stabilized by two [P(Npy)(2)(NHpy)(2)](-) anions [L](-). The packing diagram of 4 shows an interesting channel structure which contains solvated molecules of methanol and toluene. The diimine ligand [L](-), which represents the N-analogue of a phosphinate ion (H(2)PO(4)(-)), was obtained in situ under the mild reaction conditions in the absence of a base. PMID:22167162

  12. The contribution of oceanic methyl iodide to stratospheric iodine

    NASA Astrophysics Data System (ADS)

    Tegtmeier, S.; Krüger, K.; Quack, B.; Atlas, E.; Blake, D. R.; Boenisch, H.; Engel, A.; Hepach, H.; Hossaini, R.; Navarro, M. A.; Raimund, S.; Sala, S.; Shi, Q.; Ziska, F.

    2013-12-01

    We investigate the contribution of oceanic methyl iodide (CH3I) to the stratospheric iodine budget. Based on CH3I measurements from three tropical ship campaigns and the Lagrangian transport model FLEXPART, we provide a detailed analysis of CH3I transport from the ocean surface to the cold point in the upper tropical tropopause layer (TTL). While average oceanic emissions differ by less than 50% from campaign to campaign, the measurements show much stronger variations within each campaign. A positive correlation between the oceanic CH3I emissions and the efficiency of CH3I troposphere-stratosphere transport has been identified for some cruise sections. The mechanism of strong horizontal surface winds triggering large emissions on the one hand and being associated with tropical convective systems, such as developing typhoons, on the other hand, could explain the identified correlations. As a result of the simultaneous occurrence of large CH3I emissions and strong vertical uplift, localized maximum mixing ratios of 0.6 ppt CH3I at the cold point have been determined for observed peak emissions during the SHIVA (Stratospheric Ozone: Halogen Impacts in a Varying Atmosphere)-Sonne research vessel campaign in the coastal western Pacific. The other two campaigns give considerably smaller maxima of 0.1 ppt CH3I in the open western Pacific and 0.03 ppt in the coastal eastern Atlantic. In order to assess the representativeness of the large local mixing ratios, we use climatological emission scenarios to derive global upper air estimates of CH3I abundances. The model results are compared with available upper air measurements, including data from the recent ATTREX and HIPPO2 aircraft campaigns. In the eastern Pacific region, the location of the available measurement campaigns in the upper TTL, the comparisons give a good agreement, indicating that around 0.01 to 0.02 ppt of CH3I enter the stratosphere. However, other tropical regions that are subject to stronger convective

  13. The contribution of oceanic methyl iodide to stratospheric iodine

    NASA Astrophysics Data System (ADS)

    Tegtmeier, S.; Krüger, K.; Quack, B.; Atlas, E.; Blake, D. R.; Boenisch, H.; Engel, A.; Hepach, H.; Hossaini, R.; Navarro, M. A.; Raimund, S.; Sala, S.; Shi, Q.; Ziska, F.

    2013-04-01

    We investigate the contribution of oceanic methyl iodide (CH3I) to the stratospheric iodine budget. Based on CH3I measurements during three tropical ship campaigns and the Lagrangian transport model FLEXPART we provide a detailed analysis of CH3I transport from the ocean surface to the cold point in the upper tropical tropopause layer (TTL). While average oceanic emissions differ by less than 50% from campaign to campaign, the measurements show much stronger variations within each campaign. A positive correlation between the oceanic CH3I emissions and the efficiency of CH3I troposphere-stratosphere transport has been identified for some cruise sections. The mechanism of strong horizontal surface winds triggering large emissions on the one hand and being associated with tropical convective systems, such as developing typhoons, on the other hand, could explain the identified correlations. As a result of the simultaneous occurrence of large CH3I emissions and strong vertical uplift, localized maximum mixing ratios of 0.6 ppt CH3I at the cold point have been determined for observed peak emissions during the SHIVA-Sonne campaign in the coastal West Pacific. The other two campaigns give considerable smaller maxima of 0.1 ppt CH3I for the TransBrom campaign in the open West Pacific and 0.03 ppt for emissions from the coastal East Atlantic during the DRIVE campaign. In order to assess the representativeness of the large local mixing ratios we use climatological emission scenarios to derive global upper air estimates of CH3I abundances. The model results are compared to available upper air measurements including data from the recent ATTREX and HIPPO2 aircraft campaigns. In the East Pacific region, the location of the available measurement campaigns in the upper TTL, the comparisons give a good agreement indicating that around 0.01 to 0.02 ppt of CH3I enter the stratosphere. However, other tropical regions, which are subject to stronger convective activity show larger CH3I

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

    PubMed

    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

  15. Iodide Sorption to Subsurface Sediments and Illitic Minerals

    SciTech Connect

    Kaplan, D.I.; Serne, R.J.; Parker, K.E.; Kutnyakov, I.V.

    2000-01-01

    Laboratory studies were conducted to quantify and identify the key processes by which iodide (I{sup {minus}}) sorbs to subsurface arid sediments. A surprisingly large amount of I{sup {minus}} sorbed to three alkaline subsurface sediments that were low in organic matter content; distribution coefficients (K{sub d}'s) ranged from 1 to 10 mL/g and averaged 3.3 mL/g. Experiments with pure mineral isolates, similar to the minerals identified in the clay fraction of the sediments, showed that there was little or no I{sup {minus}} sorption to calcite (K{sub d} = 0.04 {+-} 0.01 mL/g), chlorite (K{sub d} = {minus}0.22 {+-} 0.06 mL/g), goethite (K{sub d} = 0.10 {+-} 0.03 mL/g), montmorillonite (K{sub d} = {minus}0.42 {+-} 0.08 mL/g), quartz (K{sub d} = 0.04 {+-} 0.02 mL/g), or vermiculite (K{sub d} = 0.56 {+-} 0.21 mL/g). Conversely, a significant amount of I{sup {minus}} sorbed to illite (K{sub d} = 15.14 {+-} 2.84 mL/g). Treating the {sup 125}I{sup {minus}}-laden illite mixtures with dissolved F{sup {minus}}, Cl{sup {minus}}, Br{sup {minus}}, or {sup 127}I{sup {minus}}, caused 43 {+-} 3%, 45 {+-} 0%, 52 {+-} 3%, and 83 {+-} 1%, respectively, of the adsorbed I{sup {minus}} to desorb. Finally, I{sup {minus}} sorption to illite was strongly pH-dependent; the K{sub d} values decreased from 46 to 22 mL/g as the pH values increased from 3.6 to 9.4. An appreciable amount of I{sup {minus}} sorbed to illite even under alkaline conditions. These experiments suggest that illite removed I{sup {minus}} from the aqueous phase predominantly by reversible physical adsorption to the pH-dependent edge sites. Illites may constitute a substantial proportion of the clay-size fraction of many arid sediments and therefore may play an important role in retarding I{sup {minus}} movement in these sediments.

  16. Iodide sorption to subsurface sediments and illitic minerals

    SciTech Connect

    Kaplan, D.I.; Serne, R.J.; Parker, K.E.; Kutnyakov, I.V.

    2000-02-01

    Laboratory studies were conducted to quantify and identify the key processes by which iodide (I{sup {minus}}) sorbs to subsurface arid sediments. A surprisingly large amount of I{sup {minus}} sorbed to three alkaline subsurface sediments that were low in organic matter content; distribution coefficients (K{sub d}'s) ranged from 1 to 10 mL/g and averaged 3.3 mL/g. Experiments with pure mineral isolates, similar to the minerals identified in the clay fraction of the sediments, showed that there was little or no I{sup {minus}} sorption to calcite (K{sub d} = 0.04 {+-} 0.01 mL/g), chlorite (K{sub d} = {minus}0.22 {+-} 0.06 mL/g), goethite (K{sub d} = 0.10 {+-} 0.03 mL/g), montmorillonite (K{sub d} = {minus}0.42 {+-} 0.08 mL/g), quartz (K{sub d} = 0.04 {+-} 0.02 mL/g), or vermiculite (K{sub d} = 0.56 {+-} 0.21 mL/g). Conversely, a significant amount of I{sup {minus}} sorbed to illite (K{sub d} = 15.14 {+-} 2.84 mL/g). Treating the {sup 125}I{sup {minus}}-laden illite mixtures with dissolved F{sup {minus}}, Cl{sup {minus}}, Br{sup {minus}}, or {sup 127}I{sup {minus}}, caused 43 {+-} 3%, 45 {+-} 0%, 52 {+-} 3%, and 83 {+-} 1%, respectively, of the adsorbed I{sup {minus}} to desorb. Finally, I{sup {minus}} sorption to illite was strongly pH-dependent; the K{sub d} values decreased from 46 to 22 mL/g as the pH values increased from 3.6 to 9.4. An appreciable amount of I{sup {minus}} sorbed to illite even under alkaline conditions. These experiments suggest that illite removed I{sup {minus}} from the aqueous phase predominantly by reversible physical adsorption to the pH-dependent edge sites. Illites may constitute a substantial proportion of the clay-size fraction of many arid sediments and therefore may play an important role in retarding I{sup {minus}} movement in these sediments.

  17. Salty glycerol versus salty water surface organization: bromide and iodide surface propensities.

    PubMed

    Huang, Zishuai; Hua, Wei; Verreault, Dominique; Allen, Heather C

    2013-07-25

    Salty NaBr and NaI glycerol solution interfaces are examined in the OH stretching region using broadband vibrational sum frequency generation (VSFG) spectroscopy. Raman and infrared (IR) spectroscopy are used to further understand the VSFG spectroscopic signature. The VSFG spectra of salty glycerol solutions reveal that bromide and iodide anions perturb the interfacial glycerol organization in a manner similar as that found in aqueous halide salt solutions, thus confirming the presence of bromide and iodide anions at the glycerol surface. Surface tension measurements are consistent with the surface propensity suggested by the VSFG data and also show that the surface excess increases with increasing salt concentration, similar to that of water. In addition, iodide is shown to have more surface prevalence than bromide, as has also been determined from aqueous solutions. These results suggest that glycerol behaves similarly to water with respect to surface activity and solvation of halide anions at its air/liquid interface. PMID:23663033

  18. Effects of synthetic retinoid Am80 on iodide-induced autoimmune thyroiditis in nonobese diabetic mice.

    PubMed

    Morohoshi, Kazuki; Yoshida, Katsumi; Nakagawa, Yoshinori; Hoshikawa, Saeko; Ozaki, Hiroshi; Takahashi, Yurie; Ito, Sadayoshi; Mori, Kouki

    2011-01-01

    We examined whether a synthetic retinoid Am80 prevented the development of autoimmune thyroiditis in iodide-treated nonobese diabetic mice, an animal model of Hashimoto's thyroiditis (HT). Am80 (0, 0.1 or 1 mg/kg/day) was orally administered in feed during the 8-week iodide treatment. While iodide ingestion effectively induced thyroiditis, Am80 administration failed to interfere with thyroiditis development and serum anti-thyroglobulin antibody levels regardless of the dose of the retinoid. Splenic T cell numbers, splenocyte proliferation and interferon-γ production were decreased in the Am80-treated mice. Our data suggest that Am80 is not a candidate for use in the prevention of HT. PMID:21601836

  19. Bromide and iodide removal from waters under dynamic conditions by Ag-doped aerogels.

    PubMed

    Sánchez-Polo, M; Rivera-Utrilla, J; von Gunten, U

    2007-02-01

    The objective of this study was to analyze the efficiency of Ag-doped aerogels in the removal of bromide and iodide from water. To test the applicability of these aerogels in water treatment, adsorption of bromide and iodide was studied under dynamic conditions using waters from Lake Zurich and a mineral water. The results obtained by using these waters showed a high breakthrough volume (V(0.02)=0.4 L) of the columns, while the height of the mass transfer zone (H(MTZ)=6.8 cm) was low, regardless of the anion under study. Bromide- and iodide-saturated columns were regenerated with NH4OH. No change in the column characteristics was observed after two regeneration treatments, regardless of the type of water considered. PMID:17109877

  20. Fundamental studies of methyl iodide adsorption in DABCO impregnated activated carbons.

    PubMed

    Herdes, Carmelo; Prosenjak, Claudia; Román, Silvia; Müller, Erich A

    2013-06-11

    Methyl iodide capture from a water vapor stream using 1,4-diazabicyclo[2.2.2]octane (DABCO)-impregnated activated carbons is, for the first time, fundamentally described here on the atomic level by means of both molecular dynamics and grand canonical Monte Carlo simulations. A molecular dynamics annealing strategy was adopted to mimic the DABCO experimental impregnation procedure in a selected slitlike carbon pore. Predictions, restricted to the micropore region, are made about the adsorption isotherms of methyl iodide, water, and nitrogen on both impregnated and bare activated carbon models. Experimental and simulated nitrogen adsorption isotherms are compared for the validation of the impregnation strategy. Selectivity analyses of the preferential adsorption toward methyl iodide over water are also reported. These simulated adsorption isotherms sum up to previous experimental studies to provide an enhanced picture for this adsorption system of widespread use at nuclear plant HVAC facilities for the capture of radioactive iodine compounds. PMID:23679202

  1. Differential potentiometric determination of perchlorate and iodide ions in industrial wastes

    SciTech Connect

    Kolbyagin, N.P.; Vlasova, E.G.; Zhilina, O.D.; Renkova, Z.S.

    1986-12-01

    The determination of perchlorates and iodides present together in industrial wastes is hampered by the fact that these anions either are precipitated by the same organic reagents or form colored complexes with similar absorption maxima. Determining them by separation or by deducting one from their sum is a multi-step analysis which takes more time and decreases accuracy. In this paper, the authors report a rapid, single-step determination of co-present perchlorate and iodide by precipitative titration with nitron solution and potentiometric indication of the equivalence point by a perchlorate-selective membrane electrode. The perchlorate and iodide determinations were unaffected by surfactant, suspensions, and ions not precipitated with nitron. A single analysis takes 15-20 minutes. This method may also be used for analyzing single salts.

  2. A theoretical study on the reaction of ozone with aqueous iodide.

    PubMed

    Gálvez, Óscar; Baeza-Romero, M Teresa; Sanz, Mikel; Pacios, Luis F

    2016-03-21

    Atmospheric iodine chemistry plays a key role in tropospheric ozone catalytic destruction, new particle formation, and as one of the possible sinks of gaseous polar elemental mercury. Moreover, it has been recently proposed that reaction of ozone with iodide on the sea surface could be the major contributor to the chemical loss of atmospheric ozone. However, the mechanism of the reaction between aqueous iodide and ozone is not well known. The aim of this paper is to improve the understanding of such a mechanism. In this paper, an ab initio study of the reaction of aqueous iodide and ozone is presented, evaluating thermodynamic data of the different reactions proposed in previous experimental studies. In addition, the structures, energetics and possible evolution of the key IOOO(-) intermediate are discussed for the first time. PMID:26906609

  3. Synthesis and Decomposition of Zinc Iodide: Model Reactions for Investigating Chemical Change in the Introductory Laboratory

    NASA Astrophysics Data System (ADS)

    Demeo, Stephen

    1995-09-01

    The purpose of this article is to discuss two colorful reactions not widely used by chemical educators in high schools or college chemistry laboratories: The synthesis of zinc iodide from its elements, zinc and iodine, and the subsequent decomposition of zinc iodide back into its elements. These reactions are important for chemistry teachers to know about because they can be performed by introductory students to understand different aspects of chemical change such as the concepts of reaction, compound, bonding, excess and limiting reactants, an empirical formula, balanced chemical equation, the conservation of matter and energy, the Law of the Conservation of Mass, and the Law of Constant Composition. These concepts, in turn, are important because they are fundamental to chemistry, are widely taught by chemistry teachers, and are deceptively difficult for introductory chemistry students to understand. The synthesis of zinc iodide has many scientific advantages over current syntheses of binary compounds from elements such as the syntheses of copper sulfide and magnesium oxide. For example, zinc iodide can be synthesized to 1% of theoretical mass in less than a half an hour and can be readily analyzed qualitatively as well as quantitatively by two different titrations. As a set of reactions, the synthesis and decomposition of zinc iodide is safe to perform, reliable, inexpensive, and does not pose a threat to the environment. The author has developed a small collection of teacher activities describing the synthesis and decomposition of zinc iodide. The activities are innovative because they contain improvements not found in the existing literature. Appropriate for high school and first year college chemistry teachers, all of the activities contain detailed procedures and discussions as well as safety and disposal requirements.

  4. Multicompartmental model for iodide, thyroxine, and triiodothyronine metabolism in normal and spontaneously hyperthyroid cats

    SciTech Connect

    Hays, M.T.; Broome, M.R.; Turrel, J.M.

    1988-06-01

    A comprehensive multicompartmental kinetic model was developed to account for the distribution and metabolism of simultaneously injected radioactive iodide (iodide*), T3 (T3*), and T4 (T4*) in six normal and seven spontaneously hyperthyroid cats. Data from plasma samples (analyzed by HPLC), urine, feces, and thyroid accumulation were incorporated into the model. The submodels for iodide*, T3*, and T4* all included both a fast and a slow exchange compartment connecting with the plasma compartment. The best-fit iodide* model also included a delay compartment, presumed to be pooling of gastrosalivary secretions. This delay was 62% longer in the hyperthyroid cats than in the euthyroid cats. Unexpectedly, all of the exchange parameters for both T4 and T3 were significantly slowed in hyperthyroidism, possibly because the hyperthyroid cats were older. None of the plasma equivalent volumes of the exchange compartments of iodide*, T3*, or T4* was significantly different in the hyperthyroid cats, although the plasma equivalent volume of the fast T4 exchange compartments were reduced. Secretion of recycled T4* from the thyroid into the plasma T4* compartment was essential to model fit, but its quantity could not be uniquely identified in the absence of multiple thyroid data points. Thyroid secretion of T3* was not detectable. Comparing the fast and slow compartments, there was a shift of T4* deiodination into the fast exchange compartment in hyperthyroidism. Total body mean residence times (MRTs) of iodide* and T3* were not affected by hyperthyroidism, but mean T4* MRT was decreased 23%. Total fractional T4 to T3 conversion was unchanged in hyperthyroidism, although the amount of T3 produced by this route was increased nearly 5-fold because of higher concentrations of donor stable T4.

  5. Crystal Structures of Multicopper Oxidase CueO Bound to Copper(I) and Silver(I): Functional Role of a Methonine-Rich Sequence

    SciTech Connect

    Singh, Satish K.; Roberts, Sue A.; McDevitt, Sylvia F.; Weichsel, Andrzej; Wildner, Guenter F.; Grass, Gregor B.; Rensing, Christopher; Montfort, William R.

    2011-10-24

    The multicopper oxidase CueO oxidizes toxic Cu(I) and is required for copper homeostasis in Escherichia coli. Like many proteins involved in copper homeostasis, CueO has a methionine-rich segment that is thought to be critical for copper handling. How such segments function is poorly understood. Here, we report the crystal structure of CueO at 1.1 {angstrom} with the 45-residue methionine-rich segment fully resolved, revealing an N-terminal helical segment with methionine residues juxtaposed for Cu(I) ligation and a C-terminal highly mobile segment rich in methionine and histidine residues. We also report structures of CueO with a C500S mutation, which leads to loss of the T1 copper, and CueO with six methionines changed to serine. Soaking C500S CueO crystals with Cu(I), or wild-type CueO crystals with Ag(I), leads to occupancy of three sites, the previously identified substrate-binding site and two new sites along the methionine-rich helix, involving methionines 358, 362, 368, and 376. Mutation of these residues leads to a {approx}4-fold reduction in kcat for Cu(I) oxidation. Ag(I), which often appears with copper in nature, strongly inhibits CueO oxidase activities in vitro and compromises copper tolerance in vivo, particularly in the absence of the complementary copper efflux cus system. Together, these studies demonstrate a role for the methionine-rich insert of CueO in the binding and oxidation of Cu(I) and highlight the interplay among cue and cus systems in copper and silver homeostasis.

  6. Toxicogenomic responses of nanotoxicity in Daphnia magna exposed to silver nitrate and coated silver nanoparticles

    EPA Science Inventory

    Applications for silver nanomaterials in consumer products are rapidly expanding, creating an urgent need for toxicological examination of the exposure potential and ecological effects of silver nanoparticles (AgNPs). The integration of genomic techniques into environmental toxic...

  7. Silver ions eluted from partially protected silver nanoparticles.

    PubMed

    Heidari Zare, Hamideh; Düttmann, Oliver; Vass, Attila; Franz, Gerhard; Jocham, Dieter

    2016-01-01

    The most prominent character of a new type of antibacterial urological catheters is the zebra-stripe pattern of a silver film, which is plated electroless on their interior wall and capped by a very thin semipermeable layer of parylene. This design effectively controls the release rate of Ag(+) ions in artificial urine, which has been measured as function of time with optical emission spectroscopy. By evaluating the minimum inhibitory concentration against certain strains of bacteria with solutions of AgNO3 of known concentration with the method of optical density and applying this analysis to the silver-eluting catheters, it was shown that this moderation prolongs the period of their application significantly. But to act as antibacterial agent in chlorine-containing solutions, as in urine, the presence of urea is required to avoid precipitation of AgCl and to meet or even exceed the minimum inhibitory concentration of Ag(+). The quality of the silver depot layer was further determined by the deposition rate and its morphology, which revealed that the film consisted of grains with a mean size of 150 nm. PMID:27400747

  8. Aquatic Toxicity Comparison of Silver Nanoparticles and Silver Nanowires

    PubMed Central

    Kim, Tae Gyu; Kim, Jin Kwon; Kim, Ellen; Lee, Ji Hyun; Chung, Young Shin

    2015-01-01

    To better understand the potential ecotoxicological impact of silver nanoparticles (AgNPs) and silver nanowires (AgNWs) released into freshwater environments, the toxicities of these nanomaterials were assessed and compared using Organization for Economic Cooperation and Development (OECD) test guidelines, including a “Daphnia sp., acute immobilization test,” “Fish, acute toxicity test,” and “freshwater alga and cyanobacteria, growth inhibition test.” Based on the estimated median lethal/effective concentrations of AgNPs and AgNWs, the susceptibility to the nanomaterials was different among test organisms (daphnia > algae > fish), suggesting that the AgNPs are classified as “category acute 1” for Daphnia magna, “category acute 2” for Oryzias latipes, and “category acute 1” for Raphidocelis subcapitata, while the AgNWs are classified as “category acute 1” for Daphnia magna, “category acute 2” for Oryzias latipes, and “category acute 2” for Raphidocelis subcapitata, according to the GHS (Globally Harmonized System of Classification and Labelling of Chemicals). In conclusion, the present results suggest that more attention should be paid to prevent the accidental or intentional release of silver nanomaterials into freshwater aquatic environments. PMID:26125025

  9. Study of semitransparent palladium contacts on mercuric iodide by photoluminescence spectroscopy and thermally stimulated current measurements

    NASA Astrophysics Data System (ADS)

    Bao, X. J.; Schlesinger, T. E.; James, R. B.; Gentry, G. L.; Cheng, A. Y.; Ortale, C.

    1991-04-01

    Semitransparent palladium contacts on mercuric iodide were studied by low temperature photoluminescence spectroscopy and thermally stimulated conductivity. These contacts were deposited either by thermal evaporation or by plasma sputtering. Changes due to palladium deposition were found in the photoluminescence spectra and were attributed to modifications in the stoichiometry within the palladium/mercuric iodide interfacial region. Thermally stimulated conductivity measurements revealed two dominant traps with activation energies of 0.010 and 0.54 eV. The importance of these traps in the application of nuclear detection is discussed.

  10. Cascade Photoredox/Iodide Catalysis: Access to Difluoro-γ-lactams via Aminodifluoroalkylation of Alkenes.

    PubMed

    Zhang, Muliang; Li, Weipeng; Duan, Yingqian; Xu, Pan; Zhang, Songlin; Zhu, Chengjian

    2016-07-01

    The novel cascade photoredox/iodide catalytic system enables the alkene to serve as a radical acceptor capable of achieving aminodifluoroalkylation of alkenes. Cheap iodide salts play a vital role in this reaction, which could tune carbocation reactivity through reversible C-I bond formation for controlling reaction selectivity, and a series of competitive reactions are completely eliminated in the presence of multiple reactivity pathways. The present dual catalytic protocol affords a very convenient method for direct synthesis of various difluoro-γ-lactams from simple and readily available starting materials under mild reaction conditions. PMID:27337532

  11. Nitrosyl iodide, INO: A combined ab initio and high-resolution spectroscopic study

    NASA Astrophysics Data System (ADS)

    Bailleux, S.; Duflot, D.; Aiba, S.; Nakahama, S.; Ozeki, H.

    2016-04-01

    In the nitrosyl halides series (XNO, where X = F, Cl, Br, I), INO is the only chemical species whose rotational spectrum has not been reported. Nitrosyl iodide, together with the nitryl (INO2), nitrite (IONO) and nitrate (IONO2) iodides, is believed to impact tropospheric ozone levels. Guided by our quantum chemical calculations, we report the detection of INO in the gas phase by high-resolution spectroscopy for the first time. INO was generated by mixing continuously I2 and NO. The measurement and least-squares analysis of 173 a-type rotational transitions resulted in the accurate determination of molecular parameters.

  12. Air-Driven Potassium Iodide-Mediated Oxidative Photocyclization of Stilbene Derivatives.

    PubMed

    Matsushima, Tomoya; Kobayashi, Sayaka; Watanabe, Soichiro

    2016-09-01

    A new method has been developed for the potassium iodide-mediated oxidative photocyclization of stilbene derivatives. Compared with conventional iodine-mediated oxidative photocyclization reactions, this new method requires shorter reaction times and affords cyclized products in yields of 45-97%. This reaction proceeds with a catalytic amount of potassium iodide and works in an air-driven manner without the addition of an external scavenger. The radical-mediated oxidative photocyclization of stilbene derivatives using TEMPO was also investigated. PMID:27508401

  13. The BLI-3/TSP-15/DOXA-1 dual oxidase complex is required for iodide toxicity in Caenorhabditis elegans.

    PubMed

    Xu, Zhaofa; Luo, Jintao; Li, Yu; Ma, Long

    2015-02-01

    Iodine is an essential trace element for life. Iodide deficiency can lead to defective biosynthesis of thyroid hormones and is a major cause of hypothyroidism and mental retardation. Excess iodide intake, however, has been linked to different thyroidal diseases. How excess iodide causes harmful effects is not well understood. Here, we found that the nematode Caenorhabditis elegans exhibits developmental arrest and other pleiotropic defects when exposed to excess iodide. To identify the responsible genes, we performed a forward genetic screen and isolated 12 mutants that can survive in excess iodide. These mutants define at least four genes, two of which we identified as bli-3 and tsp-15. bli-3 encodes the C. elegans ortholog of the mammalian dual oxidase DUOX1 and tsp-15 encodes the tetraspanin protein TSP-15, which was previously shown to interact with BLI-3. The C. elegans dual oxidase maturation factor DOXA-1 is also required for the arresting effect of excess iodide. Finally, we detected a dramatically increased biogenesis of reactive oxygen species in animals treated with excess iodide, and this effect can be partially suppressed by bli-3 and tsp-15 mutations. We propose that the BLI-3/TSP-15/DOXA-1 dual oxidase complex is required for the toxic pleiotropic effects of excess iodide. PMID:25480962

  14. Studying Equilibrium in the Chemical Reaction between Ferric and Iodide Ions in Solution Using a Simple and Inexpensive Approach

    ERIC Educational Resources Information Center

    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…

  15. Observation of nuclear quadrupole hyperfine structure in the infrared spectrum of hydrogen iodide using a tunable-diode laser

    NASA Technical Reports Server (NTRS)

    Strow, L. L.

    1980-01-01

    Nuclear quadrupole hyperfine structure has been observed in the 1-0 vibration-rotation band of hydrogen iodide with a tunable-diode laser. The measured splittings agree well with microwave measurements of the HI molecule. Evidence for a slight change in the iodine nuclear quadrupole coupling constant from the ground to first excited vibrational state in hydrogen iodide was found.

  16. AGI doubles minority geoscience scholarships

    NASA Astrophysics Data System (ADS)

    The American Geological Institute, Alexandria, Va., has had a significant increase in funds available for minority geoscience scholarships for the 1990-1991 academic year. The number of scholarships awarded this year has more than doubled from a total of 36 in 1989-90 to 80 available for 1990-1991.The increase is due largely to a grant from the National Science Foundation. Total value of the awards, which will be given to undergraduate and graduate geoscience students, will be $221,000. For 1989--990 the total value was $36,750.

  17. Application of Silver and Silver Oxide Nanoparticles Impregnated on Activated Carbon to the Degradation of Bromate.

    PubMed

    Choi, J S; Lee, H; Park, Y K; Kim, S J; Kim, B J; An, K H; Kim, B H; Jung, S C

    2016-05-01

    Silver and silver oxide nanoparticles were impregnated on the surface of powdered activated carbon (PAC) using a single-step liquid phase plasma (LPP) method. Spherical silver and silver oxide nanoparticles of 20 to 100 nm size were dipersed evenly on the surface of PAC. The impregnated PAC exhibited a higher activity for the decomposition of bromate than bare PAC. The XPS, Raman and EDX analyses showed that the Ag/PAC composites synthesized by the LPP process. PMID:27483780

  18. Electrodeposited Silver Nanoparticles Patterned Hexagonally for SERS

    SciTech Connect

    Gu, Geun Hoi; Lee, Sue Yeone; Suh, Jung Sang

    2010-08-06

    We have fabricated hexagonally patterned silver nanoparticles for surface-enhanced Raman scattering (SERS) by electrodepositing silver on the surface of an aluminum plate prepared by completely removing the oxide from anodic aluminum oxide (AAO) templates. Even after completely removing the oxide, well-ordered hexagonal patterns, similar to the shape of graphene, remained on the surface of the aluminum plate. The borders of the hexagonal pattern protruded up to form sorts of nano-mountains at both the sides and apexes of the hexagon, with the apexes protruding even more significantly than the sides. The aluminum plate prepared by completely removing the oxide has been used in the preparation of SERS substrates by sputter-coating of gold or silver on it. Instead of sputter-coating, here we have electro-deposited silver on the aluminum plate. When silver was electro-deposited on the plate, silver nanoparticles were made along the hexagonal margins.

  19. Passive particle dosimetry. [silver halide crystal growth

    NASA Technical Reports Server (NTRS)

    Childs, C. B.

    1977-01-01

    Present methods of dosimetry are reviewed with emphasis on the processes using silver chloride crystals for ionizing particle dosimetry. Differences between the ability of various crystals to record ionizing particle paths are directly related to impurities in the range of a few ppm (parts per million). To understand the roles of these impurities in the process, a method for consistent production of high purity silver chloride, and silver bromide was developed which yields silver halides with detectable impurity content less than 1 ppm. This high purity silver chloride was used in growing crystals with controlled doping. Crystals were grown by both the Czochalski method and the Bridgman method, and the Bridgman grown crystals were used for the experiments discussed. The distribution coefficients of ten divalent cations were determined for the Bridgman crystals. The best dosimeters were made with silver chloride crystals containing 5 to 10 ppm of lead; other impurities tested did not produce proper dosimeters.

  20. Preparation of silver nanoparticles at low temperature

    NASA Astrophysics Data System (ADS)

    Mishra, Mini; Chauhan, Pratima

    2016-04-01

    Silver from ancient time is used as antimicrobial agent in the bulk form but now with the advancement in nanotechnology silver in the form of nanoparticles shown potential effect against microbes which make us easy to fight with many diseases plants and animals. In this work silver nanoparticles were synthesized by chemical routes using sodium borohydride as reducing agent at low temperature. The particles were characterized through UV-Visible spectroscopy as well as X-Ray Diffraction. The UV-visible spectra of silver nanoparticles exhibited absorption at 425 cm; the crystallite size of the particles is between 19nm to 39nm. EDAX graph shows two peaks of silver and oxygen. Water absorbed by silver nanoparticles was removed by the calcinations.

  1. Silver nanocluster catalytic microreactors for water purification

    NASA Astrophysics Data System (ADS)

    Da Silva, B.; Habibi, M.; Ognier, S.; Schelcher, G.; Mostafavi-Amjad, J.; Khalesifard, H. R. M.; Tatoulian, M.; Bonn, D.

    2016-07-01

    A new method for the elaboration of a novel type of catalytic microsystem with a high specific area catalyst is developed. A silver nanocluster catalytic microreactor was elaborated by doping a soda-lime glass with a silver salt. By applying a high power laser beam to the glass, silver nanoclusters are obtained at one of the surfaces which were characterized by BET measurements and AFM. A microfluidic chip was obtained by sealing the silver coated glass with a NOA 81 microchannel. The catalytic activity of the silver nanoclusters was then tested for the efficiency of water purification by using catalytic ozonation to oxidize an organic pollutant. The silver nanoclusters were found to be very stable in the microreactor and efficiently oxidized the pollutant, in spite of the very short residence times in the microchannel. This opens the way to study catalytic reactions in microchannels without the need of introducing the catalyst as a powder or manufacturing complex packed bed microreactors.

  2. Production of Recovery of Silver for Laboratory Use.

    ERIC Educational Resources Information Center

    Hill, James W.; Bellows, Lena

    1986-01-01

    Describes a method by which teachers can either produce their own silver of "technical" quality or recycle silver chloride residues to recover the silver for similar reuse. Procedures used are outlined and economics of the method are discussed. (JN)

  3. Preparation of silver-activated zinc sulfide thin films

    NASA Technical Reports Server (NTRS)

    Feldman, C.; Swindells, F. E.

    1968-01-01

    Silver improves luminescence and reduces contamination of zinc sulfide phosphors. The silver is added after the zinc sulfide phosphors are deposited in thin films by vapor evaporation, but before calcining, by immersion in a solution of silver salt.

  4. 40 CFR 421.120 - Applicability: Description of the secondary silver subcategory.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... secondary silver subcategory. 421.120 Section 421.120 Protection of Environment ENVIRONMENTAL PROTECTION... CATEGORY Secondary Silver Subcategory § 421.120 Applicability: Description of the secondary silver... silver from secondary silver facilities processing photographic and nonphotographic raw materials....

  5. 40 CFR 421.120 - Applicability: Description of the secondary silver subcategory.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... secondary silver subcategory. 421.120 Section 421.120 Protection of Environment ENVIRONMENTAL PROTECTION... CATEGORY Secondary Silver Subcategory § 421.120 Applicability: Description of the secondary silver... silver from secondary silver facilities processing photographic and nonphotographic raw materials....

  6. 40 CFR 421.120 - Applicability: Description of the secondary silver subcategory.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... secondary silver subcategory. 421.120 Section 421.120 Protection of Environment ENVIRONMENTAL PROTECTION... CATEGORY Secondary Silver Subcategory § 421.120 Applicability: Description of the secondary silver... silver from secondary silver facilities processing photographic and nonphotographic raw materials....

  7. 40 CFR 421.120 - Applicability: Description of the secondary silver subcategory.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... secondary silver subcategory. 421.120 Section 421.120 Protection of Environment ENVIRONMENTAL PROTECTION... CATEGORY Secondary Silver Subcategory § 421.120 Applicability: Description of the secondary silver... silver from secondary silver facilities processing photographic and nonphotographic raw materials....

  8. 40 CFR 421.120 - Applicability: Description of the secondary silver subcategory.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... secondary silver subcategory. 421.120 Section 421.120 Protection of Environment ENVIRONMENTAL PROTECTION... CATEGORY Secondary Silver Subcategory § 421.120 Applicability: Description of the secondary silver... silver from secondary silver facilities processing photographic and nonphotographic raw materials....

  9. Efficiency enhancement in dye sensitized solar cells using gel polymer electrolytes based on a tetrahexylammonium iodide and MgI2 binary iodide system.

    PubMed

    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. PMID:22618351

  10. Risk assessment of silver nanoparticles

    NASA Astrophysics Data System (ADS)

    Shipelin, V. A.; Gmoshinski, I. V.; Khotimchenko, S. A.

    2015-11-01

    Nanoparticles of metallic silver (Ag) are among the most widely used products of nanotechnology. Nanosized colloidal silver (NCS) is presented in many kinds of production as solutions of particles with diameter less than 100 nm. NCS is used in a variety of fields, including food supplements, medicines, cosmetics, packaging materials, disinfectants, water filters, and many others. Problems of toxicity and related safety of NCS for humans and environmental systems are recently overestimated basing on data of numerous toxicological studies in vitro and in vivo. The article discusses the results of current studies in recent years and the data of author's own experiments on studying the safety of NCS, that allows to move on to risk assessment of this nanomaterial presented in consumer products and environmental samples.

  11. Synthesis and optical properties of silver nanoparticles

    SciTech Connect

    Singh, Jaiveer; Kaurav, Netram; Choudhary, K. K.; Okram, Gunadhor S.

    2015-07-31

    The preparation of stable, uniform silver nanoparticles by reduction of silver acetate by ethylene glycol (EG) is reported in the present paper. It is a simple process of recent interest for obtaining silver nanoparticles. The samples were characterized by X-Ray diffraction (XRD), which reveals an average particle size (D) of 38 nm. The UV/Vis spectra show that an absorption peak, occurring due to surface plasmon resonance (SPR), exists at 319 nm.

  12. Fluorescent silver nanoclusters as DNA probes

    NASA Astrophysics Data System (ADS)

    Obliosca, Judy M.; Liu, Cong; Yeh, Hsin-Chih

    2013-08-01

    Fluorescent silver nanoclusters (few atoms, quantum sized) have attracted much attention as promising substitutes for conventional fluorophores. Due to their unique environmental sensitivities, new fluorescent probes have been developed based on silver nanoclusters for the sensitive and specific detection of DNA. In this review we present the recent discoveries of activatable and color-switchable properties of DNA-templated silver nanoclusters and discuss the strategies to use these new properties in DNA sensing.

  13. Analysis of iodide and iodate in Lake Mead, Nevada using a headspace derivatization gas chromatography-mass spectrometry.

    PubMed

    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

  14. Synthesis of a Stable Primary-Alkyl-Substituted Selenenyl Iodide and Its Hydrolytic Conversion to the Corresponding Selenenic Acid.

    PubMed

    Sase, Shohei; Kakimoto, Ryo; Kimura, Ryutaro; Goto, Kei

    2015-01-01

    A primary-alkyl-substituted selenenyl iodide was successfully synthesized through oxidative iodination of a selenol with N-iodosuccinimide by taking advantage of a cavity-shaped steric protection group. The selenenyl iodide exhibited high thermal stability and remained unchanged upon heating at 100 °C for 3 h in [D₈]toluene. The selenenyl iodide was reduced to the corresponding selenol by treatment with dithiothreitol. Hydrolysis of the selenenyl iodide under alkaline conditions afforded the corresponding selenenic acid almost quantitatively, corroborating the chemical validity of the recent proposal that hydrolysis of a selenenyl iodide to a selenenic acid is potentially involved in the catalytic mechanism of an iodothyronine deiodinase. PMID:26633336

  15. Silver europium(III) polyphosphate

    PubMed Central

    Ayadi, Mounir; Férid, Mokhtar; Moine, Bernard

    2009-01-01

    Europium(III) silver polyphosphate, AgEu(PO3)4, was prepared by the flux method. The atomic arrangement is built up by infinite (PO3)n chains (periodicity of 4) extending along the c axis. These chains are joined to each other by EuO8 dodeca­hedra. The Ag+ cations are located in the voids of this arrangement and are surrounded by five oxygen atoms in a distorted [4+1] coordination. PMID:21582031

  16. Fabrication of Silver Nano-Noodles

    NASA Astrophysics Data System (ADS)

    Iwanabe, Yasuhiko; Horiuchi, Toshiyuki; Tominaga, Junji; Büchel, Dorothea; Mihalcea, Christophe

    2003-10-01

    We report that silver nanowires can easily be fabricated from organic solution including silver ions by focusing a laser beam on a light absorbing material surface. Focusing a laser beam on a Si film (100-nm thickness on a glass substrate) in silver oxide (AgOx) saturated benzoic acid (BA) (10-3 M)-2-propanol (IPA) solution produced noodle-like silver nanowires with diameters of less than 50 nm. It was suggested that the Ag nanowires were formed by super-cooling effect at local heating and solubility around the laser spot region, and transported to the laser spot area by thermal convection.

  17. Silver staining of proteins in polyacrylamide gels

    PubMed Central

    Chevallet, Mireille; Luche, Sylvie; Rabilloud, Thierry

    2006-01-01

    Silver staining is used to detect proteins after electrophoretic separation on polyacrylamide gels. It combines excellent sensitivity (in the low nanogram range) whilst using very simple and cheap equipment and chemicals. It is compatible with downstream processing such as mass spectrometry analysis after protein digestion. The sequential phases of silver staining are protein fixation, then sensitization, then silver impregnation and finally image development. Several variants of silver staining are described here, which can be completed in a time range from 2 hours to one day after the end of the electrophoretic separation. Once completed, the stain is stable for several weeks PMID:17487168

  18. Morphology of a silver/polyacrylonitrile nanocomposite

    NASA Astrophysics Data System (ADS)

    Kudryashov, M. A.; Mashin, A. I.; Tyurin, A. S.; Fedosov, A. E.; Chidichimo, G.; De Filpo, G.

    2011-01-01

    Silver/polyacrylonitrile (Ag/PAN) nanocomposites are synthesized at the stage of simultaneous acrylonitrile polymerization and the reduction of silver ions from a mixture of silver nitrate AgNO3, acrylonitrile, and a photoinitiator. The synthesized films are transparent in the visible region and are characterized by a uniform dispersion of silver nanoparticles in a PAN matrix without any macroscopic agglomeration. The effects of the metal salt and photoinitiator concentrations on the size and density of metal nanoparticles in a composite are revealed.

  19. Synthesis/characterization of a new chelating resin and on-line solid phase extraction for the determination of Ag(I) and Pd(II) from water, cream, anode slime and converter samples by flow injection flame atomic absorption spectrometry.

    PubMed

    Çetin, Tülin; Tokalioğlu, Serife; Ülgen, Ahmet; Sahan, Serkan; Özentürk, Ismail; Soykan, Cengiz

    2013-02-15

    On-line preconcentration procedures for the determination of Ag(I) and Pd(II) by flame atomic absorption spectrometry have been described. A new chelating resin, poly (N,N'-dipropionitrilemethacrylamide-co-divinylbenzene-co-2-acrylamido-2-methyl-1-propane sulfonic acid) was synthesized and used as a new adsorbent material. The resin was characterized by Fourier transform infrared spectroscopy and elemental analysis. Ag(I) was adsorbed on the chelating resin at pH 5.0 and eluted with 1.0 mol L(-1) HNO3. Pd(II) was retained at pH 9.5 and eluted with 1.5 mol L(-1) HCl. The experimental parameters (pH, type and concentration of eluent, flow rates of sample and eluent solutions, elution time and the effect of interfering ions) for both Ag(I) and Pd(II) were investigated in detail. The detection limit for Ag(I) was 2.4 μg L(-1) and the relative standard deviation was 2.9% for 0.2 μg mL(-1) Ag(I). The detection limit for Pd(II) was 1.7 μg L(-1) and the relative standard deviation was 2.8% for 0.3 μg mL(-1) Pd(II). Accuracy was confirmed by analyzing a certified reference material (TMDA-70), recovery studies on real samples and comparison with electrothermal atomic absorption analysis. The proposed methods were successfully applied to the on-line determination of Ag(I) in bottled water, pharmaceutical cream and anode slime samples and Pd(II) in bottled water and catalytic converter samples. PMID:23598028

  20. [Simultaneous determination of iodide and thiocyanate powdered milk using ion chromatography with mixed-mode column].

    PubMed

    Li, Jing; Wang, Yu; Liang, Lina

    2010-04-01

    The contents of iodide and thiocyanate are important detection items in powdered milk quality testing. Due to the complexity of the powdered milk matrix, chromatographic analysis is easily subjected to interference. Acclaim Mixed-Mode WAX-1 column incorporated both hydrophobic and weak anion-exchange properties was used to separate iodide and thiocyanate from interfering substances in powdered milk matrix, and detected by Ultraviolet (UV) detection. After powdered milk was dissolved in water, the protein was precipitated by acetonitrile. Then OnGuard RP pre-treatment column was used to remove the organic matters which might pollute the column. The eluent was acetonitrile-100 mmol/L phosphate buffer (pH 6)-water (45:5:50,v/v/v). The UV detection wavelength was 226 nm. The limits of detection of iodide and thiocyanate were 4.6 microg/L and 13.8 microg/L respectively, and the relative standard deviations of peak areas were 1.2% (n = 6) and 1.7% (n = 6) for 0.2 mg/L iodide and thiocyanate standard solutions. The method is accurate and reliable, and has wide linear range, low limit of detection. This method provides a viable approach for powdered milk quality dairy products. PMID:20712128