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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. Silver iodide sodalite for 129I immobilisation

    NASA Astrophysics Data System (ADS)

    Vance, E. R.; Gregg, D. J.; Grant, C.; Stopic, A.; Maddrell, E. R.

    2016-11-01

    Silver iodide sodalite was initially synthesised as a fine-grained major phase in a nominally stoichiometric composition following hot isostatic pressing at 850 °C with 100 MPa and its composition, Ag4Al3Si3O12I, was approximately verified by scanning electron microscopy. An alternative preparative method yielded a more dense and stoichiometric AgI sodalite on sintering and HIPing. As found for AgI, the I is released from AgI sodalite much more readily in reducing water than in ordinary water. Thus in normal PCT-B tests, the I release was <0.3 g/L in water, but it was ∼70 g/L under highly reducing conditions. This is an important point with regard to can material if HIPing is used for consolidation.

  5. 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)

  6. 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.

  7. 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

  8. 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

  9. The photophysics of ionic semiconductors at low temperatures: Silver bromide, silver iodide, and cuprous oxide

    NASA Astrophysics Data System (ADS)

    Rodney, Paul James

    Three ionic semiconductors that differ in the character of their lowest energy transitions were examined. Silver bromide (AgBr) has an indirect gap, silver iodide (AgI) a direct gap, and cuprous oxide (Cu2O) a direct but parity forbidden lowest energy transition. Donor-acceptor (D-A) pair recombination was identified in the three materials using time-resolved spectroscopy and the decay dynamics were compared to a previously developed theoretical model. Nanocrystals of each material were synthesized and the effects of quantum confinement on the low temperature recombination dynamics were studied. The dynamics of the emission from aqueous prepared nanocrystals of AgBr was compared to that of larger crystals. The observed lifetime of the free exciton increased from ~20 μs to ~600 μs as the size of the crystallite decreased from 41 to 8 nm. The D- A pair recombination kinetics were bulk-like in 41 nm AgBr while in the 8 nm samples the decay lasted longer. Factorial experiments led to methods of synthesis of nanocrystals in aqueous solvents allowing the dying of the nanocrystals. Preliminary spectroscopic evidence indicated J-aggregates of pseudoisocyanine (PIC) dye were adsorbed to the nanocrystal surface. Tabular AgI nanocrystals exhibiting one dimensional confinement were synthesized. The D-A nature of the broad luminescence observed in emission from AgI has been confirmed. The D-A emission decay rates for 0.5 μm and 52 nm crystals were indistinguishable. Quantum confinement effects are manifest in a blue shift of the emission and a loss of the longer lived decay components in ~5 nm thick tabular AgI nanocrystals. Measurements of the rise time and decay time of exciton luminescence using photoluminescence upconversion were attempted. Microcrystals and nanocrystals of Cu2O were synthesized via aqueous methods with the intention of completing previous quantum confinement studies where severely heat treated purchased Cu2O was compared to aqueous prepared poly

  10. Dielectric relaxation in AgI doped silver selenomolybdate glasses

    NASA Astrophysics Data System (ADS)

    Palui, A.; Shaw, A.; Ghosh, A.

    2016-05-01

    We report the study of dielectric properties of some silver ion conducting silver selenomolybdate mixed network former glasses in a wide frequency and temperature range. The experimental data have been analyzed in the framework of complex dielectric permittivity. The dielectric permittivity data have been well interpreted using the Cole-Cole function. The temperature dependence of relaxation time obtained from real part of dielectric permittivity data shows an Arrhenius behavior. The activation energy shows a decreasing trend with the increase of doping content. Values of stretched exponential parameter are observed to be independent of temperature and composition.

  11. 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.

  12. 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.

  13. 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

  14. 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.

  15. Ultrafast electronic relaxation processes in semiconductor nanoparticles (silver iodide, silver iodide/silver sulfide, silver bromide/silver sulfide, silver sulfide, cupric sulfide, and copper sulfide) and carotenoids

    NASA Astrophysics Data System (ADS)

    Brelle, Michael Chris

    2000-11-01

    This dissertation examines primarily the ultrafast dynamics of excited state charge carriers in semiconductor nanoparticles. The dissertation also briefly examines the excited state lifetimes of a few carotenoids. Understanding the dynamic properties of charge carriers in semiconductor nanoparticles is crucial for the further development of applications utilizing these systems. The dynamic properties including shallow and deep trapping as well as recombination have been studied in a variety of semiconductor nanoparticle systems. Kinetic modeling was utilized to assist in the assignment of all observed signals and the nature of the decays. The first observation of ultrafast trapping in silver halides was observed in AgI nanoparticles including the identification that interstitial silver ions may act as deep traps. Several interesting phenomena were observed in Ag2S and CuxS nanoparticles including dark shallow trap states and shallow trap state saturation leading to increased transient absorption over transient bleach with increasing excitation intensity. These observations have provided further insight into the relaxation pathways for charge carriers in semiconductor nanoparticle systems. Lifetimes of the S2 excited states of four carotenoids have also been determined. The S2 lifetime for beta-carotene was confirmed from previous fluorescence up-conversion experiments whereas the S2 lifetimes that were previously unknown for three carotenoids, violaxanthin, neaxanthin, and lutein were discovered. These experiments together demonstrate the capabilities of femtosecond pump-probe spectroscopy to characterize and better understand the processes involved in the ultrafast relaxation events in both molecular and nanoparticle systems.

  16. Speciation of silver nanoparticles and Ag(I) species using cloud point extraction followed by electrothermal atomic absorption spectrometry

    NASA Astrophysics Data System (ADS)

    López-García, Ignacio; Vicente-Martínez, Yesica; Hernández-Córdoba, Manuel

    2014-11-01

    Silver nanoparticles in the presence of Triton-X114 were extracted into a micellar phase obtained after incubation at 40 °C for 10 min followed by centrifugation. After injection of an aliquot (30 μL) of the surfactant-rich phase into the electrothermal atomizer, the enrichment effect due to cloud point extraction allowed a detection limit of 2 ng L- 1 silver to be achieved. The preconcentration factor was 242, and the repeatability for ten measurements at a 50 ng L- 1 silver level was 4.6%. Ag(I) species were adsorbed onto the silver nanoparticles and were also extracted in the micellar phase. The incorporation of 0.01 mol L- 1 ammonium thiocyanate to the sample solution prevented the extraction of Ag(I) species. Speciation was carried out using two extractions, one in the absence and the other in the presence of thiocyanate, the concentration of Ag(I) species being obtained by difference. The procedure was applied to the determination of silver nanoparticles and Ag(I) species in waters and in lixiviates obtained from sticking plasters and cleaning cloths.

  17. The Persistence of Seeding Effects in a Winter Orographic Cloud Seeded with Silver Iodide Burned in Acetone.

    NASA Astrophysics Data System (ADS)

    Deshler, Terry; Reynolds, David W.

    1990-06-01

    A single case-study of a winter orographic cloud over the central Sierra Nevada is presented in which the effects of aerial seeding with silver iodide, an AgI NH4C1O4 mixture burned in acetone, were observed to persist for over 90 min after seeding and 100 km downwind of the seedline. A research aircraft was able to locate and track the line source of AgI using an ice nucleus counter. High ice crystal concentrations due to seeding were not apparent until more than one hour after seeding. This may have been partially due to the high natural concentrations of ice, but post-mission analysis revealed that most sampling passes during the first hour following seeding were made below the AgI seeded volume. Ice nucleus measurements confirmed sampling of the seedline from 1-1.5 h after seeding, with associated increases in ice crystal concentrations. The effectiveness of the seeding material in the field was higher than laboratory measurements would suggest.

  18. Laser-based synthesis of core Ag-shell AgI nanoparticles

    NASA Astrophysics Data System (ADS)

    Tan, Hua; Fan, Wai Yip

    2005-05-01

    A laser-controlled synthesis of silver iodide (AgI) nanoparticles with isolable AgI shell-Ag core stable intermediates is achieved via molecular iodine photodissociation in the presence of pure Ag nanoparticles dispersed in water. Ag nanoparticles were introduced into the solution containing sodium dodecylsulphate surfactants and iodine by ablating a piece of silver foil with a 532 nm pulsed Nd-YAG laser. Transmission electron microscopy images showed that different AgI shell-Ag core sizes could be achieved by controlling the photolysis of I 2 in solution. These nanoparticles were also found to catalyse an atom-economy Grignard-Barbier organic reaction.

  19. 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.

  20. Fluoride-induced reduction of Ag(I) cation leading to formation of silver mirrors and luminescent Ag-nanoparticles.

    PubMed

    Maity, Krishnendu; Panda, Dillip K; Lochner, Eric; Saha, Sourav

    2015-03-01

    In aprotic solvents, Lewis basic F(-) anion reduces Lewis acidic Ag(I) cation to Ag(0), forming metallic silver mirrors on the inner surfaces of reaction vessels and luminescent Ag-nanoparticles (AgNPs) in supernatant solutions, which emit blue light upon UV irradiation. The F(-)-induced formation of silver mirrors and AgNPs was confirmed through X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS), fluorescence spectroscopy, and mass spectrometry, whereas the Ag(I)-induced oxidation of F(-) to Ḟ radical, followed by its conversion to HF2(-) via H-abstraction and H-bonding, was evident from (19)F NMR spectroscopy. This redox reaction is deactivated in water, as the reducing power of hydrated F(-) diminishes drastically. Less Lewis basic Cl(-), Br(-), and I(-) ions do not reduce Ag(I) to Ag(0), instead they can only form Ag(I) halide precipitates irrespective of protic or aprotic solvents. The Ag-coated surfaces, luminescent AgNPs, and Ḟ radicals produced by this unprecedented redox reaction could be exploited as electrodes, light-emitting materials, and radical initiators, respectively.

  1. 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

  2. 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.

  3. 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.

  4. Photocharging of thin films of silver iodide and its relevance to the Daguerre photographic process

    NASA Astrophysics Data System (ADS)

    Brodie, I.; Thackray, M.

    1984-12-01

    In the Daguerre photographic process1-3, a polished silver-coated plate is exposed to iodine vapour, thereby forming a very thin film of silver iodide, usually about 30-nm thick4. After exposure, the image is developed by mercury vapour, which condenses preferentially where light has fallen, amalgamating with silver liberated from the silver iodide (and possibly with the substrate). The remaining silver iodide is dissolved with an aqueous photographic fixing solution (sodium thiosulphate). When viewed at most angles, a positive image of the scene is seen as areas of amalagam (diffusely reflecting), which appear white, on areas of polished silver (specularly reflecting), which appear black. The sharpness with which edges were reproduced in several old daguerreotypes led us to suspect that electrostatic processes might be involved, and we now report two experiments which confirm that.

  5. Microphysical Effects of Wintertime Cloud Seeding with Silver Iodide over the Rocky Mountains. Part III: Observations over the Grand Mesa, Colorado.

    NASA Astrophysics Data System (ADS)

    Super, Arlin B.; Boe, Bruce A.

    1988-10-01

    During March 1986, several airborne and ground-based silver iodide (AgI) seeding experiments were conducted over the Grand Mesa, Colorado, during a three-day period of northerly flow and shallow orographic cloud. While little natural snowfall was observed during these experiments, supercooled liquid water formed over the windward slopes and evaporated to the lee of the mesa of many hours. Seeding-induced microphysical changes coincident with the AgI plumes were found in all eight experiments, (including two that employed ground-based seeding) by aircraft sampling about 500 m above the mesa top. Precipitation rates estimated from ice particle images at light levels suggested increases within the seeded volumes in all but one experiment. Surface precipitation increases were observed in three aircraft seeding experiments and one ground-based seeding experiment that coincided with the passage of AgI plumes aloft. Surface observations were not possible during the other ground-based seeding experiment, but some increase in snowfall is thought probable. Three aircraft seeding experiments failed to show surface snowfall increases, and reasons for this are explored.

  6. 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.

  7. 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.

  8. Investigation of silver-impregnated alumina for removal of radioactive methyl iodide

    SciTech Connect

    Funabashi, Kiyomi; Fukasawa, Tetsuo; Kikuchi, Makoto

    1995-03-01

    The removal efficiency of methyl iodide for silver-impregnated alumina from gaseous waste has been experimentally evaluated as a function of atmospheric relative humidity. A new adsorbent has been developed for the iodine filter installed in the off-gas treatment system of a radioactive waste tank vent. To improve its removal efficiency under a highly humid atmosphere, the optimum average pore size of alumina was determined to be {approximately}60 nm, and the most effective chemical form of the impregnated silver was identified as silver nitrate. Holding capability of the impregnated silver was also improved by developing a double-pore-structure alumina.

  9. 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.

  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. 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

  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. 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.

  14. 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.

  15. 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

    2015-03-02

    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.

  16. 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

  17. Study of Relaxation Dynamics in Mixed Iodide Doped Silver-Vanado-Borate Superionic Glass System

    NASA Astrophysics Data System (ADS)

    Sharma, Poonam; Kanchan, D. K.; Pant, Meenakshi; Gondaliya, Nirali; Jayswal, Manish S.

    2011-07-01

    Electrical conductivity and impedance measurements were carried out for a new mixed metal iodide salt doped silver vanado-borate i.e., [(PbI2-CuI)-Ag2O-V2O5-B2O3] super-ionic glass system. The impedance plots (Z″ vs. Z') for all the prepared glass samples were recorded and found to exhibit depressed semi circles over the studied temperature range. Frequency dependence of the imaginary part of impedance Z″ and the imaginary part of modulus M″ at different temperatures were also investigated. Also, relaxation dynamics in framework of modulus formalism has been discussed.

  18. 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.

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

    PubMed

    Chapman, Karena W; Chupas, Peter J; Nenoff, Tina M

    2010-07-01

    The effective capture and storage of radiological iodine ((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. PMID:20550110

  20. 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

  1. 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

  2. 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.

  3. 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

  4. 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.

  5. 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.

  6. 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

  7. 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.

  8. Microphysical Effects of Wintertime Cloud Seeding with Silver Iodide over the Rocky Mountains. Part II: Observations over the Bridger Range, Montana.

    NASA Astrophysics Data System (ADS)

    Super, Arlin B.; Heimbach, James A., Jr.

    1988-10-01

    During January 1985 six aircraft sampling flights were made in cloud over the target area of an earlier randomized exploratory cloud seeding experiment in the Bridger Range, Montana. One of the two diver iodide (AgI) generator sites used in the earlier experiment was operated well up the wed (windward) slope of the north-south oriented Main Ridge, Crosswind aircraft sampling was done to within 300 m above the secondary ridge target about 17 km downwind of the AgI generator.The AgI plume was detected over the target area on each of the six missions and was generally 5-8 km wide. Three of the missions detected supercooled liquid water (SLW) in the region of the AgI plume. The ice particle concentration (IPC) averaged about an order of magnitude higher in the seeded zone in these cases, and the estimated precipitation rate was greater, as compared with crosswind control zones. Most seeded ice particles were small hexagonal plates, appropriate for the prevailing temperatures and moisture conditions. The AgI generator was deliberately turned off in one of the experiments. and the seeding effects decreased with time beginning about one hour later.The other three missions sampled negligible SLW in the seeded region over the target area. Observations did not indicate detectable changes in ice particle concentrations, sizes or habits.The results of this series of physical experiments are in agreement with statistical suggestions from the earlier randomized experiment. It appears that seeding the stable orographic clouds over the Bridger Range sometimes caused marked increases in IPC, presumably leading to more surface snowfall. The physical observations indicate that enhanced IPC was largely dependent upon the availability of SLW when temperatures were cold enough for AgI nucleation.

  9. Microphysical Effects of Wintertime Cloud Seeding with Silver Iodide over the Rocky Mountains. Part I: Experimental Design and Instrumentation.

    NASA Astrophysics Data System (ADS)

    Super, Arlin B.; Boe, Bruce A.; Holroyd, Edmond W., III; Heimbach, James A., Jr.

    1988-10-01

    A series of winter orographic cloud seeding experiments is described in which the seeding agent and associated changes in cloud microphysics are monitored to within 300 m of the target areas (Montana and Colorado), and at the surface (Colorado only). This, the first paper in a three-part series, discusses the underlying physical hypothesis and experimental approach, and describes in detail the instrumentation used. The results of the physical evaluations, presented in Parts II and III, show that marked microphysical changes were caused by both ground-based and aircraft seeding with silver iodide.

  10. Effect of Mixed Glass Former on Ionic Conductivity of Silver Boro Tungstate glass system x[0.75AgI:0.25AgCl]: (1-x) [Ag2O-{B2O3:WO3}

    NASA Astrophysics Data System (ADS)

    Dehariya, Harsha; Kumar, R.; Polu, A. R.

    2012-05-01

    The idea to explore new 'Superionic Electrolytes', "Fast ionic conductors" is due to their tremendous potential applications in solid state electrochemical devices viz. solid state batteries, fuel cells, sensors, super capacitors. Superionic glasses have attracted great deal of attention due to their several advantageous over their crystalline counterparts such as high ionic conductivity, easy preparation, wide selection of compositions, isotropic properties and high stability etc [4-7]. Large numbers of silver ion based glasses have been reported in the literature for the glassy system of AgI:Ag2O: MxOy (MxOy = B2O3, SiO2, P2O5, GeO2, V2O5, As2O5, CrO3, SeO2, MoO3 & TeO3 etc many of them shows high silver ion conductivity [8]. Ion transport behavior of Silver Boro Tungstate glass system x[0.75AgI:0.25AgCl]: (1-x) [Ag2O{B2O3:WO3}], where 0 <= x <= 1 in molar wt% prepared by melt quench technique were reported. The new host [0.75AgI:0.25AgCl] was used as a better alternate in place of conventional host salt AgI. Conductivity measurement were carried out on this glass system as a function of frequency from 50 Hz to 5 MHz, over a temperature range of 27°C to 200°C, for different compositions by Impedance spectroscopy. The composition 0.7[0.75AgI:0.25AgCl]: 0.3[Ag2O{B2O3:WO3}] shows the highest conductivity of the order of σrt ~ 2.76 × 10-2 S/cm, referred to as the Optimum Conducting Composition (OCC). The enhancement in the conductivity has been obtained by mixed former effect. XRD result shows that the system is completely amorphous. Temperature dependence of conductivity of all compositions were studied & reported. Activation energies (Ea) were also evaluated from the slope of .Log(σ) vs 1000/T, Arrhenius plots.

  11. 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.

  12. AgI plumes in WRF LES simulations versus airborne measurements

    NASA Astrophysics Data System (ADS)

    Xue, L.; Rasmussen, R.; Breed, D. W.

    2011-12-01

    Inadequate or uncertain targeting of seedable clouds from silver iodide (AgI) ground-based generators has been a complex and hence a long-standing problem in winter orographic cloud seeding programs. To address this issue within the Wyoming Weather Modification Pilot Program (WWMPP), a focused field experiment was conducted between 9 February and 1 March 2011. Airborne measurements of AgI-generated ice nuclei (IN) plumes from ground-based generators were carried out by Weather Modification Inc. using a Piper Cheyenne II research aircraft equipped with an updated NCAR acoustic IN counter. The airborne data were collected over the Wyoming Medicine Bow and Sierra Madre mountain ranges on nine different days within the experimental period. This study explores the ability of the Weather Research and Forecast (WRF) model to reproduce reasonable AgI plumes by comparing the model results with these airborne measurements. A suite of WRF simulations, including 2.5 km and 500 m runs along with two 100-m resolution Large Eddy Simulations (LES), have been conducted for the 16 February case over the Medicine Bow range. Two different sets of gridded data, the North America Regional Reanalysis data and the WWMPP Real-Time Four-Dimensional Data Assimilation WRF forecast data, were used to drive the model independently. An AgI point-source module was applied to represent the release of AgI from the ground generators. A detailed description of the WRF LES results and comparisons with the airborne measurements will be presented at the conference.

  13. 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

  14. 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.

  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. 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..

  17. Size-controlled stabilization of the superionic phase to room temperature in polymer-coated AgI nanoparticles.

    PubMed

    Makiura, Rie; Yonemura, Takayuki; Yamada, Teppei; Yamauchi, Miho; Ikeda, Ryuichi; Kitagawa, Hiroshi; Kato, Kenichi; Takata, Masaki

    2009-06-01

    Solid-state ionic conductors are actively studied for their large application potential in batteries and sensors. From the view of future nanodevices, nanoscaled ionic conductors are attracting much interest. Silver iodide (AgI) is a well-known ionic conductor for which the high-temperature alpha-phase shows a superionic conductivity greater than 1 Omega(-1) cm(-1). Below 147 degrees C, alpha-AgI undergoes a phase transition into the poorly conducting beta- and gamma-polymorphs, thereby limiting its applications. Here, we report the facile synthesis of variable-size AgI nanoparticles coated with poly-N-vinyl-2-pyrrolidone (PVP) and the controllable tuning of the alpha- to beta-/gamma-phase transition temperature (Tc). Tc shifts considerably to lower temperatures with decreasing nanoparticle size, leading to a progressively enlarged thermal hysteresis. Specifically, when the size approaches 10-11 nm, the alpha-phase survives down to 30 degrees C--the lowest temperature for any AgI family material. We attribute the suppression of the phase transition not only to the increase of the surface energy, but also to the presence of defects and the accompanying charge imbalance induced by PVP. Moreover, the conductivity of as-prepared 11 nm beta-/gamma-AgI nanoparticles at 24 degrees C is approximately 1.5 x 10(-2) Omega(-1) cm(-1)--the highest ionic conductivity for a binary solid at room temperature. The stabilized superionic phase and the remarkable transport properties at a practical temperature reported here suggest promising applications in silver-ion-based electrochemical devices.

  18. Size-controlled stabilization of the superionic phase to room temperature in polymer-coated AgI nanoparticles

    NASA Astrophysics Data System (ADS)

    Makiura, Rie; Yonemura, Takayuki; Yamada, Teppei; Yamauchi, Miho; Ikeda, Ryuichi; Kitagawa, Hiroshi; Kato, Kenichi; Takata, Masaki

    2009-06-01

    Solid-state ionic conductors are actively studied for their large application potential in batteries and sensors. From the view of future nanodevices, nanoscaled ionic conductors are attracting much interest. Silver iodide (AgI) is a well-known ionic conductor for which the high-temperature α-phase shows a superionic conductivity greater than 1Ω-1cm-1 (ref. 6). Below 147∘C, α-AgI undergoes a phase transition into the poorly conducting β- and γ-polymorphs, thereby limiting its applications. Here, we report the facile synthesis of variable-size AgI nanoparticles coated with poly-N-vinyl-2-pyrrolidone (PVP) and the controllable tuning of the α- to β-/γ-phase transition temperature (Tc↓). Tc↓ shifts considerably to lower temperatures with decreasing nanoparticle size, leading to a progressively enlarged thermal hysteresis. Specifically, when the size approaches 10-11nm, the α-phase survives down to 30∘C-the lowest temperature for any AgI family material. We attribute the suppression of the phase transition not only to the increase of the surface energy, but also to the presence of defects and the accompanying charge imbalance induced by PVP. Moreover, the conductivity of as-prepared 11nm β-/γ-AgI nanoparticles at 24∘C is ~1.5×10-2Ω-1cm-1-the highest ionic conductivity for a binary solid at room temperature. The stabilized superionic phase and the remarkable transport properties at a practical temperature reported here suggest promising applications in silver-ion-based electrochemical devices.

  19. Determination of iodide in urine by ion-pair chromatography with electrochemical detection.

    PubMed

    Below, H; Kahlert, H

    2001-10-01

    A variety of parameters affecting the determination of iodide in biological materials by ion-pair chromatography and electrochemical detection were examined in detail. It became apparent that the pH value, the ion-pair concentration, the proportion of organic solvent and of organic bases as a component of the buffer solution, as well as the salt concentration in the eluent system could effectively influence the retention characteristics of iodide in the chromatographic system, resulting in the separation of potential interfering substances. The presence of other anions in the sample matrix has to be taken into consideration, particularly thiocyanate because of its long retention time. Investigations of the electrochemical detection mechanism revealed that the reaction hitherto assumed to be responsible for detector signal generation (formation of AgI) is incorrect. In addition, a much more sensitive detection of iodide than that cited in the literature to date is possible if the detector potential is optimally selected and any anticipated interfering substances are removed by chromatography. Use of a gold electrode rather than a silver electrode also considerably enhances the reliability of the procedure.

  20. 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).

  1. Mid-IR and far-IR investigation of AgI-doped silver diborate glasses

    SciTech Connect

    Hudgens, J.J.; Martin, S.W.

    1996-03-01

    The structures of {ital x}AgI+(1{minus}{ital x})Ag{sub 2}O{center_dot}2B{sub 2}O{sub 3} glasses, where 0.2{le}{ital x}{le}0.6, have been investigated using mid- and far-infrared spectroscopy. The mid-IR spectra revealed that in those glasses prepared using AgNO{sub 3} as the starting material for Ag{sub 2}O, the BO{sub 4}{sup {minus}}/BO{sub 3} ratio is constant with increasing amounts of AgI as would be expected form the proposed behavior of AgI in these glasses. However, a survey of the literature revealed those glasses prepared from pure Ag{sub 2}O show a strong linear dependence of the BO{sub 4}{sup {minus}}/BO{sub 3} ratio on AgI content. Most probably, in those glasses prepared with Ag{sub 2}O the Ag{sub 2}O/B{sub 2}O{sub 3} ratio changes with AgI content due to the decomposition of Ag{sub 2}O during melting. This different behavior is associated with AgNO{sub 3} decomposing to Ag{sub 2}O with heating followed by incorporation into the glassy network. For Ag{sub 2}O used directly, it is proposed that it decomposes to Ag metal and O{sub 2}(gas) with heating before it can be incorporated into the borate network. This latter behavior decreases with increasing AgI in the batch composition because AgI lowers the liquidus temperature of the melt considerably. The far-IR analysis of the AgI-doped silver diborate glasses suggests that there are three coordination environments for the Ag{sup +} ions; one with iodide anions and the other two with oxygen ions. It is proposed that the separate oxygen coordination environments for the Ag{sup +} ions arise from one with bridging oxygens of BO{sub 4}{sup {minus}} units, and the other with nonbridging oxygens on BO{sub 3}{sup {minus}} units. Furthermore, it is proposed that the Ag{sup +} ions in the iodide-ion environments progressively agglomerate into disordered regions of AgI, but do not form structures similar to {alpha}-AgI. (Abstract Truncated)

  2. 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 should only ...

  3. 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.

  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. 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

  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.

  7. 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

  8. 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...

  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. Liquid-phase microextraction-gas chromatography-mass spectrometry for the determination of bromate, iodate, bromide and iodide in high-chloride matrix.

    PubMed

    Reddy-Noone, Kishan; Jain, Archana; Verma, Krishna K

    2007-05-01

    In the determination of bromate and iodate, any free bromide and iodide present was quantitatively removed by anion exchange with silver chloride exploiting the differences in silver salts solubility product, being AgCl, 1.8 x 10(-10), AgBr, 5.0 x 10(-13), AgI, 8.3 x 10(-17), AgBrO(3), 5.5 x 10(-5) and AgIO(3), 3.1 x 10(-8). The oxyhalides were reduced with ascorbic acid to halides and converted to 4-bromo-2,6-dimethylaniline and 4-iodo-2,6-dimethylaniline by their reaction with 2-iodosobenzoate in the presence of 2,6-dimethylaniline at pH 6.4 and 2-3, respectively. Single drop microextraction (SDME) of the haloanilines in 2 microl of toluene and injection of the whole extract into GC-MS, or liquid-phase microextraction (LPME) into 50 microl of toluene and injection of 2 microl of extract, resulted in a sensitive method for bromate and iodate. The latter method of extraction has been found more robust, sensitive and to give better extraction in shorter period than SDME. Total bromine/iodine was determined without any treatment with silver chloride. High concentration of chloride in the matrix did not interfere. A rectilinear calibration graph was obtained for 0.05 microg-25 mg l(-1) of bromate/bromide and iodate/iodide, the limit of detection were 20 ng l(-1) of bromate, 15 ng l(-1) of iodate, 20 ng l(-1) of bromide and 10 ng l(-1) of iodide (by LPME in 50 microl of toluene). The method has been applied to seawater and table salt. From the pooled data, the average recovery of spiked oxyhalide/halide to real samples was in range 96.7-105.7% with RSD in range 1.6-6.5%. PMID:17391685

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

    DOE PAGES

    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

  13. 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.

  14. 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.

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

    DOE PAGES

    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

  16. 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

  17. 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.

  18. 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.

  19. Variable charge and electrical double layer of mineral-water interfaces: silver halides versus metal (hydr)oxides.

    PubMed

    Hiemstra, Tjisse

    2012-11-01

    Classically, silver (Ag) halides have been used to understand thermodynamic principles of the charging process and the corresponding development of the electrical double layer (EDL). A mechanistic approach to the processes on the molecular level has not yet been carried out using advanced surface complexation modeling (SCM) as applied to metal (hydr)oxide interfaces. Ag halides and metal (hydr)oxides behave quite differently in some respect. The location of charge in the interface of Ag halides is not a priori obvious. For AgI(s), SCM indicates the separation of interfacial charge in which the smaller silver ions are apparently farther away from the surface than iodide. This charge separation can be understood from the surface structure of the relevant crystal faces. Charge separation with positive charge above the surface is due to monodentate surface complex formation of Ag(+) ions binding to I sites located at the surface. Negative surface charge is due to the desorption of Ag(+) ions out of the lattice. These processes can be described with the charge distribution (CD) model. The MO/DFT optimized geometry of the complex is used to estimate the value of the CD. SCM reveals the EDL structure of AgI(s), having two Stern layers in series. The inner Stern layer has a very low capacitance (C(1) = 0.15 ± 0.01 F/m(2)) in comparison to that of metal (hydr)oxides, and this can be attributed to the strong orientation of the (primary) water molecules on the local electrostatic field of the Ag(+) and I(-) ions of the surface (relative dielectric constant ε(r) ≈ 6). Depending on the extent of water ordering, mineral surfaces may in principle develop a second Stern layer. The corresponding capacitance (C(2)) will depend on the degree of water ordering that may decrease in the series AgI (C(2) = 0.57 F/m(2)), goethite (C(2) = 0.74 F/m(2)), and rutile (C(2) = ∞), as discussed. The charging principles of AgI minerals iodargyrite and miersite may also be applied to minerals

  20. 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.

  1. 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.

  2. 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

  3. 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

  4. Silver nanoparticle-algae interactions: oxidative dissolution, reactive oxygen species generation and synergistic toxic effects.

    PubMed

    He, Di; Dorantes-Aranda, Juan José; Waite, T David

    2012-08-21

    The short-term toxicity of citrate-stabilized silver nanoparticles (AgNPs) and ionic silver Ag(I) to the ichthyotoxic marine raphidophyte Chattonella marina has been examined using the fluorometric indicator alamarBlue. Aggregation and dissolution of AgNPs occurred after addition to GSe medium while uptake of dissolved Ag(I) occurred in the presence of C. marina. Based on total silver mass, toxicity was much higher for Ag(I) than for AgNPs. Cysteine, a strong Ag(I) ligand, completely removed the inhibitory effects of Ag(I) and AgNPs on the metabolic activity of C. marina, suggesting that the toxicity of AgNPs was due to the release of Ag(I). Synergistic toxic effects of AgNPs/Ag(I) and C. marina to fish gill cells were observed with these effects possibly attributable to enhancement in the generation of reactive oxygen species by C. marina on exposure of the organism to silver.

  5. Investigation of electrode processes on th Pt/. cap alpha. -AgI boundary with the aid of estance measurements

    SciTech Connect

    Tarasov, A.Y.; Filyaev, A.T.; Karpachev, S.V.; Prusov, V.A.

    1985-10-01

    It was established that elemental silver is deposited on Pt after the latter is brought into contact with AgI and the temperature is held constant. The dependence of the estance on the electrode potential is shown; the potential was varied by causing anodic polarization relative to a silver reference electrode. The profile of the oscillogram presented is described. The decrease of estance may be explained on the basis of the theories on the influence of adsorption process on the estance, if it is assumed that the occurrence of the electrode reaction which results in the appearance of adsorbed iodine on the interface, becomes appreciable at potentials more positive than +130 mV.

  6. 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

  7. 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.

  8. 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

  9. 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

  10. Photodetectors for the Advanced Gamma-ray Imaging System (AGIS)

    NASA Astrophysics Data System (ADS)

    Wagner, Robert G.; Advanced Gamma-ray Imaging System AGIS Collaboration

    2010-03-01

    The Advanced Gamma-Ray Imaging System (AGIS) is a concept for the next generation very high energy gamma-ray observatory. Design goals include an order of magnitude better sensitivity, better angular resolution, and a lower energy threshold than existing Cherenkov telescopes. Each telescope is equipped with a camera that detects and records the Cherenkov-light flashes from air showers. The camera is comprised of a pixelated focal plane of blue sensitive and fast (nanosecond) photon detectors that detect the photon signal and convert it into an electrical one. Given the scale of AGIS, the camera must be reliable and cost effective. The Schwarzschild-Couder optical design yields a smaller plate scale than present-day Cherenkov telescopes, enabling the use of more compact, multi-pixel devices, including multianode photomultipliers or Geiger avalanche photodiodes. We present the conceptual design of the focal plane for the camera and results from testing candidate! focal plane sensors.

  11. Characterization, kinetics and thermodynamics of Ag(I) sorption using novel sorbent: Dry wheatgrass.

    PubMed

    Shah, Kruti R; Tipre, Devayani R; Dave, Shailesh R

    2016-12-01

    In the present study, dried wheatgrass (DWG), an available and renewable biomass, was investigated as a novel Ag(I) sorbent. Sorption data was modeled to 11 different kinetic and diffusion models at different DWG concentration. Pseudo-second-order model fits the data most appropriately among these. Diffusion was not the sole mechanism controlling Ag(I) sorption by DWG. The enthalpy and entropy for Ag(I) sorption by DWG are 10.511 kJ mol(-1) and 0.065 kJ mol(-1) K(-1), respectively. Gibbs free energy decreases with rise in temperature. Ag(I) sorption by DWG is spontaneous, endothermic with increased randomness at the interface. Characterization of DWG suggested the presence of diverse functional groups. Ag(I) sorption by DWG involved mechanisms such as physisorption and chemisorptions. DWG can be efficiently used to remediate and recover Ag(I) from solution in an eco-friendly manner. PMID:27260662

  12. A simple way to prepare Cupric oleate capped AgI nanoparticles

    SciTech Connect

    Song Meirong; Zhang Zhijun . E-mail: s234soow@henu.edu.cn

    2004-12-02

    Cupric oleate capped AgI (Cu(OA){sub 2}-AgI) nanoparticles were prepared by a simple method and they have good dispersibility in organic solvents. X-ray diffraction (XRD), transmission electron microscope (TEM), FTIR, X-ray photoelectron spectrometer (XPS) and ultraviolet-visible (UV-vis) spectrometer were used to characterize the Cu(OA){sub 2}-AgI nanoparticles. The results show that the mean size is about 80 nm; the modified reagent has been chemically bonded on the surface of AgI. In addition, new absorption peaks in the UV region appear.

  13. 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.

  14. Time-resolved optical study on the charge carrier dynamics in a TiO{sub 2}/AgI sandwich colloid

    SciTech Connect

    Fitzmaurice, D.; Frei, H.; Rabani, J. |

    1995-06-01

    Preparation of a sandwich colloid involving TiO{sub 2} and AgI (hexagonal) particles in alkaline aqueous solution is described. Time-resolved optical absorption experiments are reported that involve pulsed laser excitation at 355 nm (TiO{sub 2} bandgap) and at 410 nm (AgI bandgap). Charge carrier dynamics was probed directly by transient absorption measurements in the near-infrared and by reaction with methyl viologen (MV{sup 2+}). Reduction of MV{sup 2+} was observed to occur over a period of 100-200 {mu}s. MV{sup +} so produced reduced AgI to silver. By contrast, MV{sup 2+} reduction upon bandgap excitation of neat alkaline TiO{sub 2} colloid was complete within 1 {mu}s. These observations signal a prolonged electron-hole separation in the case of the AgI/TiO{sub 2} sol and indicate the formation of sandwich particles. 33 refs., 5 figs.

  15. Reduction of Ag(I), Au(III), Cu(II), and Hg(II) by Fe(II)/Fe(III) hydroxysulfate green rust.

    PubMed

    O'Loughlin, Edward J; Kelly, Shelly D; Kemner, Kenneth M; Csencsits, Roseann; Cook, Russell E

    2003-11-01

    Green rusts are mixed Fe(II)/Fe(III) hydroxides that are found in many suboxic environments where they are believed to play a central role in the biogeochemical cycling of iron. X-ray absorption fine structure analysis of hydroxysulfate green rust suspensions spiked with aqueous solutions of AgCH(3)COO, AuCl(n)(OH)(4-n), CuCl(2), or HgCl(2) showed that Ag(I), Au(III), Cu(II), and Hg(II) were readily reduced to Ag(0), Au(0), Cu(0), and Hg(0). Imaging of the resulting solids from the Ag(I)-, Au(III)-, and Cu(II)-amended green rust suspensions by transmission electron microscopy indicated the formation of submicron-sized particles of Ag(0), Au(0), and Cu(0). The facile reduction of Ag(I), Au(III), Cu(II), and Hg(II) to Ag(0), Au(0), Cu(0), and Hg(0), respectively, by green rust suggests that the presence of green rusts in suboxic soils and sediments can have a significant impact on the biogeochemistry of silver, gold, copper, and mercury, particularly with respect to their mobility.

  16. 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 ...

  17. 21 CFR 184.1265 - Cuprous iodide.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... Substances Affirmed as GRAS § 184.1265 Cuprous iodide. (a) Cuprous iodide (copper (I) iodide, CuI, CAS Reg. No. 7681-65-4) is a pure white crystalline powder. It is prepared by the reaction of copper...

  18. 21 CFR 184.1265 - Cuprous iodide.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... Substances Affirmed as GRAS § 184.1265 Cuprous iodide. (a) Cuprous iodide (copper (I) iodide, CuI, CAS Reg. No. 7681-65-4) is a pure white crystalline powder. It is prepared by the reaction of copper...

  19. 21 CFR 184.1265 - Cuprous iodide.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... Substances Affirmed as GRAS § 184.1265 Cuprous iodide. (a) Cuprous iodide (copper (I) iodide, CuI, CAS Reg. No. 7681-65-4) is a pure white crystalline powder. It is prepared by the reaction of copper...

  20. [Determination of trace metals in biological materials by iodides extraction and atomic absorption spectrometry].

    PubMed

    Sekiguchi, E; Yamamoto, K; Takano, K; Tutumi, M; Uehara, K; Ohno, T; Tasaka, S

    1983-09-01

    Extraction of arsenic, mercury, gold, silver, antimony, indium, bismuth, tellurium, cadmium, zinc and copper iodides with methylisobutylketone was examined in the sulfuric acid of concentrations from 0 to 15 normalities. Although, arsenic and zinc iodides were extracted from 6 to 12 normalities, extraction of other metal-iodides were carried out in more wide range of sulfuric acid concentrations almost from 2 to 12 normalities. Iron, sodium, potassium, magnesium and calcium iodides, these, being chief biological elements of inorganic substances, were not extracted in the least into methylisobutylketone layer from sulfuric acid solution. Copper and zinc were normal elements of biological materials and were extracted into methylisobutylketone layer by this procedures. The flame interferences of copper and zinc were not recognized in determinations of gold, silver, antimony, indium, bismuth, tellurium and cadmium. To investigate the influences of biological elements, mock solutions of human blood and urine were prepared. The addition of mock blood does not excessively interfere with determinations of arsenic, mercury, indium, bismuth, tellurium, cadmium, silver and antimony with the exception of gold. However, with addition of mock urine negative interferences were strongly seen in antimony determination, while in mercury, indium and silver determinations only slight interferences were observed. To examine the influences of sample preparation techniques, gold, silver, indium, cadmium and copper were treated both by wet ashing (nitric acid and sulfuric acid) and dry ashing.(ABSTRACT TRUNCATED AT 250 WORDS)

  1. Atomic Gravitational Wave Interferometric Sensors (AGIS) in Space

    NASA Astrophysics Data System (ADS)

    Sugarbaker, Alex; Hogan, Jason; Johnson, David; Dickerson, Susannah; Kovachy, Tim; Chiow, Sheng-Wey; Kasevich, Mark

    2012-06-01

    Atom interferometers have the potential to make sensitive gravitational wave detectors, which would reinforce our fundamental understanding of gravity and provide a new means of observing the universe. We focus here on the AGIS-LEO proposal [1]. Gravitational waves can be observed by comparing a pair of atom interferometers separated over an extended baseline. The mission would offer a strain sensitivity that would provide access to a rich scientific region with substantial discovery potential. This band is not currently addressed with the LIGO or LISA instruments. We analyze systematic backgrounds that are relevant to the mission and discuss how they can be mitigated at the required levels. Some of these effects do not appear to have been considered previously in the context of atom interferometry, and we therefore expect that our analysis will be broadly relevant to atom interferometric precision measurements. Many of the techniques relevant to an AGIS mission can be investigated in the Stanford 10-m drop tower.[4pt] [1] J.M. Hogan, et al., Gen. Rel. Grav. 43, 1953-2009 (2011).

  2. 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.

  3. Iodide transport and breast cancer.

    PubMed

    Poole, Vikki L; McCabe, Christopher J

    2015-10-01

    Breast cancer is the second most common cancer worldwide and the leading cause of cancer death in women, with incidence rates that continue to rise. The heterogeneity of the disease makes breast cancer exceptionally difficult to treat, particularly for those patients with triple-negative disease. To address the therapeutic complexity of these tumours, new strategies for diagnosis and treatment are urgently required. The ability of lactating and malignant breast cells to uptake and transport iodide has led to the hypothesis that radioiodide therapy could be a potentially viable treatment for many breast cancer patients. Understanding how iodide is transported, and the factors regulating the expression and function of the proteins responsible for iodide transport, is critical for translating this hypothesis into reality. This review covers the three known iodide transporters - the sodium iodide symporter, pendrin and the sodium-coupled monocarboxylate transporter - and their role in iodide transport in breast cells, along with efforts to manipulate them to increase the potential for radioiodide therapy as a treatment for breast cancer.

  4. An organic redox electrolyte to rival triiodide/iodide in dye-sensitized solar cells.

    PubMed

    Wang, Mingkui; Chamberland, Nathalie; Breau, Livain; Moser, Jacques-E; Humphry-Baker, Robin; Marsan, Benoît; Zakeeruddin, Shaik M; Grätzel, Michael

    2010-05-01

    Dye-sensitized solar cells (DSCs) have achieved impressive conversion efficiencies for solar energy of over 11% with an electrolyte that contains triiodide/iodide as a redox couple. Although triiodide/iodide redox couples work efficiently in DSCs, they suffer from two major disadvantages: electrolytes that contain triiodide/iodide corrode electrical contacts made of silver (which reduces the options for the scale up of DSCs to module size) and triiodide partially absorbs visible light. Here, we present a new disulfide/thiolate redox couple that has negligible absorption in the visible spectral range, a very attractive feature for flexible DSCs that use transparent conductors as current collectors. Using this novel, iodide-free redox electrolyte in conjunction with a sensitized heterojunction, we achieved an unprecedented efficiency of 6.4% under standard illumination test conditions. This novel redox couple offers a viable pathway to develop efficient DSCs with attractive properties for scale up and practical applications.

  5. Synthesis and structural characterization of mixed-metal complexes of Cu(I) with MOS3 cores (M = Mo, W) and of an unusual polymeric AgI/mercaptoimidazole complex with five different Ag(I) coordination environments.

    PubMed

    Beheshti, Azizollah; Clegg, William; Khorramdin, Rahman; Nobakht, Valiollah; Russo, Luca

    2011-03-28

    Reaction of (NH(4))(2)[MO(2)S(2)] (M = Mo or W) with KI, CuCl and 1,3-diazepane-2-thione (Diap) in acetone affords air- and moisture-stable mixed-metal cluster compounds [MOS(3)(CuDiap)(3)]I (1 and 2). Attempts to produce [WS(4)Ag(2)(Mim(Ph))(4)] (Mim(Ph) = 2-mercapto-1-phenylimidazole) led to the unexpected polymeric compound [Ag(5)I(5)(Mim(Ph))(4)](n) (4), subsequently obtained from a rational direct reaction between AgI and Mim(Ph) in chloroform. The complexes have been characterized by IR, (1)H and (13)C NMR spectroscopy, and single-crystal diffraction. 1 and 2 have crystallographic threefold rotation symmetry, with an incomplete distorted cube MS(3)Cu(3) core bearing terminal oxo and Diap ligands on M and Cu, respectively. The cube vertex opposite M is empty, giving an overall +1 cationic cluster and a separate I(-) anion too distant from the three Cu atoms to be considered as covalently bonded and resulting in discrete ion pairs in the crystal structures. This arrangement is different from previously reported related OMS(3)(CuL)(3)X complexes (L = monodentate ligand, X = halide), in which X, when present, is directly bonded to one, two or three Cu atoms. 4 has a one-dimensional polymeric chain structure in which silver displays five different approximately tetrahedral coordination environments, iodide ions serve as μ(2), μ(3) and μ(4) bridges, and the thione ligands are each either terminal or bridging. This unusually complex structure for a relatively simple chemical formula represents only the fifth example of a complex (AgI)(n)L(m) in which L is a neutral S-donor ligand, and the five structures display a wide range of individual features. In all three of the new structures, N-H···S and/or N-H···I hydrogen bonds are found.

  6. 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.

  7. 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.

  8. Photostimulated Luminescence and Dynamics of AgI and Ag Nanoclusters in Zeolites

    SciTech Connect

    Chen, Wei; Joly, Alan G.; Roark, Joel

    2002-06-15

    The photoluminescence and photostimulated luminescence of Ag and AgI nanoclusters formed in zeolite-Y are studied using fluorescence spectroscopy. The photoluminescence spectra of AgI nanoclusters show emission from both AgI and Ag nanoclusters, while the in the photostimulated luminescence, only the emission of Ag clusters is observed. While the photoluminescence from both Ag and AgI particles displays both sub-nanosecond and microsecond lifetimes, the emission from photostimulated luminescence shows very short, picosecond lifetimes. A model which ascribes the photostimulated luminescence to recombination of electrons trapped in the zeolite with Ag in close proximity to the trap site is proposed. The appearance of strong photostimulated luminescence with short decays in these systems demonstrates that nanoparticles have potential for digital storage and medical radiology applications.

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

    NASA Astrophysics Data System (ADS)

    Hanna, David S.; Buckley, J. H.; Falcone, A.; Fegan, S.; Finley, J.; Guarino, V.; Kaaret, P.; Krawczynski, H.; Krennrich, F.; Konopelko, A.; Romani, R.; Vassilliev, V.; Optical System Working Group; AGIS Collaboration

    2008-03-01

    The concept of a future ground-based gamma-ray observatory, AGIS, in the energy range 20 GeV-200 TeV is based on an array of 50-200 imaging atmospheric Cherenkov telescopes (IACTs). The anticipated improvement of AGIS sensitivity, angular resolution, and reliability of operation imposes demanding technological and cost requirements on the design of IACTs. In this submission we will focus on the optical system (OS) of AGIS telescopes and consider options which include traditional Davies-Cotton and the other prime-focus telescope designs, as well as the novel two-mirror aplanatic OS originally proposed by Schwarzschild. The emerging new mirror production technologies based on replication processes, such as cold and hot glass slumping, cured CFRP, and electroforming, provide new opportunities for cost effective solutions for the design of the OS. We initially evaluate capabilities of these mirror fabrication methods for the AGIS project.

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

    NASA Astrophysics Data System (ADS)

    Vassiliev, Vladimir; Buckley, Jim; Falcone, Abe; Fegan, Steven; Finley, John; Gaurino, Victor; Hanna, David; Kaaret, Philip; Konopelko, Alex; Krawczynski, Henric; Romani, Roger; Weekes, Trevor

    2008-04-01

    AGIS is a conceptual design for a future ground-based gamma-ray observatory based on an array of ˜100 imaging atmospheric Cherenkov telescopes (IACTs) with a sensitivity to gamma-rays in the energy range 40 GeV-100 TeV. The anticipated improvement of AGIS sensitivity, angular resolution, and reliability of operation imposes demanding technological and cost requirements on the design of the IACTs. In this submission we focus on the optical system (OS) of the AGIS telescopes and consider options which include traditional Davies-Cotton and the other prime- focus telescope designs, as well as a novel two-mirror aplanatic OS originally proposed by Schwarzschild. Emerging new mirror production technologies based on replication processes such as cold and hot glass slumping, cured CFRP, and electroforming provide new opportunities for cost effective solutions for the design of the OS. We evaluate the capabilities of these mirror fabrication methods for the AGIS project.

  11. 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

  12. 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.

  13. 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...

  14. 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 ...

  15. 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.

  16. 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.

  17. 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...

  18. 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...

  19. 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...

  20. 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....

  1. 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...

  2. 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....

  3. 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...

  4. 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....

  5. A convenient iodination method for alcohols using cesium iodide/methanesulfonic acid and its comparison using cesium iodide/p-toluenesulfonic acid or cesium iodide/aluminium chloride.

    PubMed

    Khan, Khalid Mohammed; Zia-Ullah; Perveen, Shahnaz; Hayat, Safdar; Ali, Muhammad; Voelter, Wolfgang

    2008-01-01

    In situ generation of hydrogen iodide from cesium iodide/methanesulfonic acid was found to be an attractive reagent combination for the conversion of alkyl, allyl, and benzyl alcohols to their corresponding iodides under mild conditions. The method is compared with that using cesium iodide/p-toluenesulfonic acid or cesium iodide/aluminium chloride.

  6. 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

  7. 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.

  8. 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.

  9. 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.

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

    NASA Astrophysics Data System (ADS)

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

    2008-12-01

    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 ~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.

  11. 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.

  12. The durability of iodide sodalite

    NASA Astrophysics Data System (ADS)

    Maddrell, Ewan; Gandy, Amy; Stennett, Martin

    2014-06-01

    An iodide sodalite wasteform has been prepared by Hot Isostatic Pressing of powder produced by hydrothermal synthesis. The wasteform was free of leachable secondary phases which can mask leaching mechanisms. Leaching is by congruent dissolution and leach rates decrease as Si and Al accumulate in the leachate. Differential normalised leach rates are 0.005-0.01 g m-2 d-1 during the 7-14 day period. This indicates that sodalite dissolution in natural groundwater, already saturated in these elements, will be very low.

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

    PubMed

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

    2013-08-01

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

  14. Green, microwave-assisted synthesis of silver nanoparticles using bamboo hemicelluloses and glucose in an aqueous medium.

    PubMed

    Peng, Hong; Yang, Anshu; Xiong, Jianghua

    2013-01-01

    A green, straightforward, microwave-assisted method of synthesizing silver nanoparticles in an aqueous medium was developed using bamboo hemicelluloses as stabilizer and glucose as reducer. The effects of irradiation time as well as initial concentrations of hemicelluloses, glucose, and AgNO(3) on the silver nanoparticle formation were studied. The silver nanoparticles were characterized by UV-vis spectroscopy, transmission electron microscopy (TEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). The results indicated the formation of spherical, nanometer-sized particles. The reaction parameters significantly affected the formation rate, size and distribution of the silver nanoparticles. The average particle size was 8.3-14.8 nm based on TEM analysis. XRD analysis revealed that the particles calcined at 300 °C were face-centered cubic. XPS characterization showed that silver Ag(0) coexisted with silver Ag(I). The synthesis process of silver nanoparticles was rapid and eco-friendly.

  15. Safe disposal of radioactive iodide ions from solutions by Ag2O grafted sodium niobate nanofibers.

    PubMed

    Mu, Wanjun; Li, Xingliang; Liu, Guoping; Yu, Qianhong; Xie, Xiang; Wei, Hongyuan; Jian, Yuan

    2016-01-14

    Radioactive iodine isotopes are released into the environment by the nuclear industry and medical research institutions using radioactive materials, and have negative effects on organisms living within the ecosystem. Thus, safe disposal of radioactive iodine is necessary and crucial. For this reason, the uptake of iodide ions was investigated in Ag2O nanocrystal grafted sodium niobate nanofibers, which were prepared by forming a well-matched phase coherent interface between them. The resulting composite was applied as an efficient adsorbent for I(-) anions by forming an AgI precipitate, which also remained firmly attached to the substrates. Due to their one-dimensional morphology, the new adsorbents can be easily dispersed in liquids and readily separated after purification. This significantly enhances the adsorption efficiency and reduces the separation costs. The change in structure from the pristine sodium niobate to Ag2O anchored sodium niobate and to the used adsorbent was examined by using various characterization techniques. The effects of Ag(+) concentration, pH, equilibration time, ionic strength and competing ions on the iodide ion removal ability of the composite were studied. The Ag2O nanocrystal grafted sodium niobate adsorbent showed a high adsorption capacity and excellent selectivity for I(-) anions in basic solutions. Our results are useful for the further development of improved adsorbents for removing I(-) anions from basic wastewater.

  16. Refractive Index of Sodium Iodide

    SciTech Connect

    Jellison Jr, Gerald Earle; Boatner, Lynn A; Ramey, Joanne Oxendine; Kolopus, James A; Ramey, Lucas A; Singh, David J

    2012-01-01

    The refractive index of sodium iodide, an important scintillator material that is widely used for radiation detection, is based on a single measurement made by Spangenberg at one wavelength using the index-matching liquid immersion method (Z. Kristallogr., 57, 494-534 (1923)). In the present paper, we present new results for the refractive index of sodium iodide as measured by the minimum deviation technique at six wavelengths between 436 nm (n=1.839 0.002) and 633 nm (n=1.786 0.002). These 6 measurements can be fit to a Sellmeier model, resulting in a 2 of 1.02, indicating a good fit to the data. In addition, we report on ellipsometry measurements, which suggest that the near-surface region of the air sensitive NaI crystal seriously degrades, even in a moisture-free environment, resulting in a significantly lower value of the refractive index near the surface. First-principles theoretical calculations of the NaI refractive index that agree with the measured values within 0.025-0.045 are also presented and discussed.

  17. 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.

  18. Factors affecting the retention of methyl iodide by iodide-impregnated carbon

    SciTech Connect

    Hyder, M.L.; Malstrom, R.A.

    1990-12-31

    Iodide-impregnated activated carbon that had been in use for up to 30 months was studied to characterize those factors that affect its interaction with and retention of methyl iodide. Humidity and competing organic sorbents were observed to decrease the residence time of the methyl iodide on the carbon bed. Additionally, changes in the effective surface area and the loss of iodide from the surface are both important in determining the effectiveness of the carbon for retaining radioactive iodine from methyl iodide. A simple model incorporating both factors gave a fairly good fit to the experimental data.

  19. Factors affecting the retention of methyl iodide by iodide-impregnated carbon

    SciTech Connect

    Hyder, M.L.; Malstrom, R.A.

    1990-01-01

    Iodide-impregnated activated carbon that had been in use for up to 30 months was studied to characterize those factors that affect its interaction with and retention of methyl iodide. Humidity and competing organic sorbents were observed to decrease the residence time of the methyl iodide on the carbon bed. Additionally, changes in the effective surface area and the loss of iodide from the surface are both important in determining the effectiveness of the carbon for retaining radioactive iodine from methyl iodide. A simple model incorporating both factors gave a fairly good fit to the experimental data.

  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. 75 FR 65526 - AGY Holding Corporation, Huntingdon, PA; Notice of Revised Determination on Reconsideration

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-10-25

    ... certification, are eligible to apply for adjustment assistance under Chapter 2 of Title II of the Trade Act of... Determination on Reconsideration By application dated June 1, 2010 a union official requested administrative... of AGY Holding Corporation, Huntingdon, Pennsylvania, to apply for Trade Adjustment Assistance...

  2. 21 CFR 582.5634 - Potassium iodide.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... DRUGS, FEEDS, AND RELATED PRODUCTS SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients and/or Dietary Supplements 1 § 582.5634 Potassium iodide. (a) Product. Potassium iodide. (b) Tolerance. 0.01 percent. (c... salt as a source of dietary iodine in accordance with good manufacturing or feeding practice....

  3. 21 CFR 582.5634 - Potassium iodide.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... DRUGS, FEEDS, AND RELATED PRODUCTS SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients and/or Dietary Supplements 1 § 582.5634 Potassium iodide. (a) Product. Potassium iodide. (b) Tolerance. 0.01 percent. (c... salt as a source of dietary iodine in accordance with good manufacturing or feeding practice....

  4. 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.

  5. Development and validation of an assay for iodide in serum using ion chromatography with pulsed amperometric detection.

    PubMed

    Kaiser, Edward; Shaffer, Lydia; Flaherty, John M; Rohrer, Jeffrey S; Himmelstein, Matthew W

    2009-05-01

    We developed and validated an ion chromatography method to assay iodide in serum sampled from rats and rabbits that had been exposed to iodomethane. Iodomethane is of interest because it is a volatile liquid pre-plant soil crop protection fumigant that has been proposed as a non-ozone-depleting alternative to methyl bromide. Serum was prepared from whole blood collected on wet ice at the time of sacrifice and kept frozen at less than -65 degrees C. For analysis, serum samples were thawed unassisted at ambient temperature. Proteins were separated from the serum samples by ultrafiltration. A 100-microl filtered serum sample was then injected into the ion chromatograph without additional sample preparation. Iodide was separated in <20 min by anion-exchange chromatography using a 25-mM nitric acid eluent. The analyte of interest was detected by pulsed amperometry using a silver working electrode. The method showed linear response over the concentration range of 100 to 5000 ng/ml iodide (r2>.998) with a lower limit of quantitation of 100 ng/ml iodide. The accuracy of the procedure, determined by spiked recovery measurements at 100 ng/ml iodide, was between 90 and 110%. A method detection limit of 20 ng/ml for iodide in serum samples was demonstrated using the method of standard additions.

  6. 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

  7. 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

  8. 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.

  9. Two 2D silver(I) coordination polymers derived from mixed ligands: Syntheses, structures, photoluminescent and thermal properties

    NASA Astrophysics Data System (ADS)

    Liu, Fu-Jing; Sun, Di; Li, Yun-Hua; Hao, Hong-Jun; Huang, Rong-Bin; Zheng, Lan-Sun

    2011-07-01

    Two isomers of the aminobenzonitrile were reacted with Ag 2O and phthalic acid under ultrasonic condition, yielding two coordination polymers (CPs) of the formula [Ag 2( o-abn)(pa)] n ( 1) and [Ag 4( m-abn)(pa) 2] n ( 2). They have been characterized by elemental analysis, IR spectrum and single crystal X-ray diffraction. Both complexes 1 and 2 are 2D sheet structures which contain two different Ag(I) aggregates, 1D silver helical chain and 2D silver sheet for 1 and 2, respectively. The o-abn in 1 adopts a rare tridentate μ 3- N, N' N' mode to bridge the neighboring 1D silver chains to form a 2D coordination network, while the m-abn ligand just acts as a monodentate N-donor in 2 and does not contribute to the extension of the 2D silver sheet to the higher dimensionality. As the change of the relative position of amino and cyano groups of the aminobenzonitrile ligand, the dimensionality of the Ag(I) aggregates in 1 and 2 increases from 1D to 2D, which indicates that the relative positions of amino and cyano groups of aminobenzonitrile play an important role in the formation of the diverse Ag(I) aggregates, as a consequence, different 2D coordination networks are produced. Additionally, results about emissive behaviors and thermal stabilities of them are discussed.

  10. 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

  11. 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.

  12. Thermoelectric properties of molten Bi2Te3, CuI, and AgI

    NASA Astrophysics Data System (ADS)

    Nishikawa, Kazutaka; Takeda, Yasuhiko; Motohiro, Tomoyoshi

    2013-01-01

    To achieve large figure of merit (ZT) and superior thermal durability at high temperatures, we have investigated thermoelectric properties of molten Bi2Te3, CuI, and AgI up to 1173 K. Molten Bi2Te3 was found to have large electrical conductivity between 1800 and 2000 (Ω ṡ cm)-1. Molten CuI and AgI, however, exhibited small electrical conductivity less than 1 (Ω ṡ cm)-1, nevertheless they show very large Seebeck coefficients over 800 μV/K. We estimated thermal conductivity using Wiedemann Franz law and the model established by Regel et al. [Phys. Status Solidi A 5, 13 (1971)]. The evaluated ZT for CuI is over 0.1.

  13. Camera Concepts for the Advanced Gamma-Ray Imaging System (AGIS)

    NASA Astrophysics Data System (ADS)

    Nepomuk Otte, Adam

    2009-05-01

    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. Each telescope is equipped with a camera that detects and records the Cherenkov-light flashes from air showers. The camera is comprised of a pixelated focal plane of blue sensitive and fast (nanosecond) photon detectors that detect the photon signal and convert it into an electrical one. The incorporation of trigger electronics and signal digitization into the camera are under study. Given the size of AGIS, the camera must be reliable, robust, and cost effective. We are investigating several directions that include innovative technologies such as Geiger-mode avalanche-photodiodes as a possible detector and switched capacitor arrays for the digitization.

  14. 1-Alkenylcalcium iodide: synthesis and stability.

    PubMed

    Köhler, Mathias; Görls, Helmar; Langer, Jens; Westerhausen, Matthias

    2014-04-25

    To enhance the scope of heavy calcium-based Grignard reagents, 1,2-dihydro-4-iodonaphthalene (1) was reduced with calcium in THF giving tetrakis(thf) (1,2-dihydronaphth-4-yl)calcium iodide (2). This derivative represents a 1-alkenylcalcium complex based on X-ray structure determination and NMR data. The stability of this compound is significantly reduced compared with the aromatic naphthylcalcium iodide. PMID:24677436

  15. 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.

  16. 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.

  17. Absorption spectra of AgI at pressures to 136 kbar

    SciTech Connect

    Liebenberg, D.H.; Hudson, J.

    1981-01-01

    Spectral absorption measurements in AgI are reported at pressures up to 136 kbar using a diamond anvil cell. In the NaCl phase between 5 and 70 kbar the absorption edge shift is found to be nearly linear with pressure. No indication of a sudden jump into a CsCl phase is found near 100 kbar and the possible influence of larger pressure gradients in earlier measurements is discussed.

  18. Iodide transport: implications for health and disease

    PubMed Central

    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

  19. 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

  20. 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.

  1. Synthesis of novel chitosan resin possessing histidine moiety and its application to the determination of trace silver by ICP-AES coupled with triplet automated-pretreatment system.

    PubMed

    Hosoba, Minako; Oshita, Koji; Katarina, Rosi K; Takayanagi, Toshio; Oshima, Mitsuko; Motomizu, Shoji

    2009-04-20

    A novel chitosan resin, cross-linked chitosan functionalized with histidine moiety (histidine-type chitosan resin), was synthesized for the collection and concentration of trace silver in aquatic samples. A triplet automated-pretreatment system (Triplet Auto-Pret System) installed mini-columns packed with the synthesized histidine-type chitosan resin was coupled with an inductively coupled plasma-atomic emission spectrometry (ICP-AES) for a rapid and sensitive analysis. Adsorption behavior of 50 elements on the histidine-type chitosan resin was examined. A trace amount of Ag(I) was shown a good adsorption in wide pH regions (pH 5-9), and Ag(I) adsorbed was readily recovered with 1 M nitric acid solution. The limit of detection (3sigma) for silver was 0.03 microg L(-1). The system was successfully applied to river water and dipped water in silver coated container.

  2. 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.

  3. 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.

  4. 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

  5. Glass formation and high conductivity in the ternary system AgI + Ag/sub 3/AsO/sub 4/ + AgPO/sub 3/: host to glassy AgI

    SciTech Connect

    Martin, S.W.; Schiraldi, A.

    1985-05-09

    Wide regions of glass formation have been found in the ternary system xAgI + yAg/sub 3/AsO/sub 4/ + (1 - x - y)AgPO/sub 3/. Glasses containing up to 75 mol % AgI can be formed in sections greater than 2 cm thick without signs of devitrification. Glass transition temperatures as high as 175/sup 0/C for glasses containing approx. 10 mol% AgI fall to approx. 45/sup 0/C at the highest AgI content. An equivalent ratio of AgI:N is defined and it is found that, for all glass-forming compositions, the electrical data as expressed in the Arrhenius form, sigma = A exp(-E/sub act/RT), log (sigma/omega cm)/sup -1/), log (A/omega cm)/sup -1/), E/sub act//(kcal mol/sup -1/), and additionally T/sub g/K, can be described as linear functions of N. These data are used to give support to the view of these glasses as being hosts to a liquidlike AgI giving rise to the high conductivity they exhibit, as high as 0.0143 (omega cm)/sup -1/ at room temperature for glasses containing the maximum AgI. Finally, from these linear relationships, functions for the mobility ..mu.. and number of the mobile Ag/sup +/ cations n are developed. 29 references, 8 figures, 2 tables.

  6. Silver Hazards to Fish, Wildlife, and Invertebrates: A Synoptic Review

    USGS Publications Warehouse

    Eisler, R.

    1996-01-01

    Ecological and toxicological aspects of silver (Ag) in the environment are briefly summarized with an emphasis on natural resources. Elevated silver concentrations in biota occur in the vicinities of sewage outfalls, electroplating plants, mine waste sites, and silver-iodide seeded areas; in the United States, the photography industry is the major source of anthropogenic silver discharges into the biosphere. Silver and its compounds are not known to be mutagenic, teratogenic, or carcinogenic. Under normal routes of exposure, silver does not pose serious environmental health problems to humans at less than 50.0 ug total Ag/L drinking water or 10.0 ug per cubic meter air. Free silver ion, however, was lethal to representative species of sensitive aquatic plants, invertebrates, and teleosts at nominal water concentrations of 1.2 to 4.9 ug/L; sublethal effects were significant between 0.17 and 0.6 ug/L. Silver was harmful to poultry at concentrations as low as 1.8 mg total Ag/kg whole egg fresh weight by way of injection, 100.0 mg total Ag/L in drinking water, or 200.0 mg total Ag/kg in diets; sensitive mammals were adversely affected at total silver concentrations as low as 250.0 ug/L in drinking water, 6.0 mg/kg in diets, or 13.9 mg/kg whole body.

  7. Glycosyl iodides. History and recent advances.

    PubMed

    Meloncelli, Peter J; Martin, Alan D; Lowary, Todd L

    2009-06-12

    The use of glycosyl iodides as an effective method for the preparation of glycosides has had a recent resurgence in carbohydrate chemistry, despite its early roots in which these species were believed to be of limited use. Renewed interest in these species as glycosylating agents has been spurred by their demonstrated utility in the stereoselective preparation of O-glycosides, and other glycosylic compounds. This review provides a brief historical account followed by an examination of the use of glycosyl iodides in the synthesis of oligosaccharides and other glycomimetics, including C-glycosylic compounds, glycosyl azides and N-glycosides.

  8. Recovery of silver from CEPOD anolyte solutions

    SciTech Connect

    Blanchard, D.L.; Surma, J.E.; Alexander, D.L.; Shade, E.H.; Matheson, J.D.; Cochran, D.L.; Wheelwright, E.J.; Boyd, T.

    1994-09-01

    The process known as Catalyzed Electrochemical Plutonium Oxide Dissolution (CEPOD) has been shown effective for removing plutonium from a variety of residues and solids. This process involves the electrochemical oxidation of PuO{sub 2} (and other Pu species) to (PuO{sub 2}){sup 2+}, and dissolution of the latter species in the anode solution (anolyte). Silver is used to transfer charge from the electrodes to the solid Pu oxide. Ag (1) is oxidized at the anode to Ag(II) and carried by the solution to the plutonium oxide solids, where the silver and oxide undergo a redox reaction that converts Pu(IV) to Pu(VI), and Ag(II) to Ag(I). Other metal ions [such as Ce(IV) and Co(III)] may also be used for this charge transfer, but have been found to be less effective than silver. The same process may be used to destroy various organic materials (such as paper and wood, oil and fuels, and synthetic polymer materials) by complete oxidation to CO{sub 2} or H{sub 2}O, for example. Upon completion of a CEPOD dissolver run, the anolyte may be processed to remove solution species of interest (i.e., Pu), or the anolyte may be recycled, or disposed. Because silver is a Resource Conservation and Recovery Act (RCRA) land ban material, it must be removed from waste streams. Preliminary experiments, completed in FY 1991, demonstrated a simple, effective technique for silver removal from solutions. Ascorbic acid (C{sub 6}H{sub 8}O{sub 6}) Was Used to reduce silver ion to metallic silver, which precipitates from solution. The process was demonstrated effective on a bench scale using samples of actual CEPOD anolyte. Further experiments, in FY 1993, optimized these parameters and demonstrated the effectiveness of the technique on CEPOD anolyte on a larger, process scale (liters of solution). This report describes both the preliminary bench-scale experiments and the more recent process-scale experiments. The results are also compared to electro-deposition, another method of silver ion removal.

  9. 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

  10. 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.

  11. 21 CFR 184.1265 - Cuprous iodide.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... the following specific limitations: Category of food Maximum treatment level in food Functional use... 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...

  12. 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.

  13. 21 CFR 184.1265 - Cuprous iodide.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Cuprous iodide. 184.1265 Section 184.1265 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) DIRECT FOOD... accordance with § 184.1(b)(2), the ingredient is used in food only within the following specific...

  14. 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…

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

    SciTech Connect

    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.

  16. Pressure Dependence of Anharmonic Effective Pair Potentials in Rock Salt Type AgI

    SciTech Connect

    Yoshiasa, Akira; Sugahara, Masahiko; Fukui, Hiroshi; Arima, Hiroshi; Ohtaka, Osamu; Okube, Maki; Katayama, Yoshinori; Murai, Kei-ichiro

    2007-02-02

    Pressure dependence of anharmonic effective pair potentials V(u)=au2/2+bu3/3{exclamation_point} for the I-Ag bond in rock salt type AgI has been investigated by EXAFS Debye-Waller factors. EXAFS measurements near the I K-edge were performed under pressure up to 6.0 GPa using a multi-anvil high-pressure device and synchrotron radiation from SPring-8, Hyogo. The potential parameter a for rock-salt type is 1.66(5) eV/A2 at 1.0 GPa and increases to 1.88(6) eV/A2 at 6.0 GPa. The phonon energies in rock salt type AgI under pressure have been estimated using the potential parameter a by calculating the dynamical matrix. The anharmonic effective pair potential for each phase is influenced by pressure and becomes steeper with increasing pressure while the extent of anharmonicity decreases with pressure.

  17. 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

  18. 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.

  19. 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.

  20. 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

  1. Hexanuclear Platinum(II) Thiolate Macrocyclic Host: Charge-Transfer-Driven Inclusion of a Ag(I) Ion Guest.

    PubMed

    Shichibu, Yukatsu; Yoshida, Keisuke; Konishi, Katsuaki

    2016-09-19

    The inclusion of a Ag(I) ion by a hexanuclear platinum(II) thiolate macrocycle in solution was demonstrated, and the inclusion structure was determined by X-ray crystallography. Unique host-guest intermetallic interactions driven by charge transfer were elucidated by optical absorption spectroscopy and theoretical calculations. PMID:27608203

  2. 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.

  3. 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.

  4. 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

  5. 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

  6. 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.

  7. Methyl iodide production in the open ocean

    NASA Astrophysics Data System (ADS)

    Stemmler, I.; Hense, I.; Quack, B.; Maier-Reimer, E.

    2014-08-01

    Production pathways of the prominent volatile organic halogen compound methyl iodide (CH3I) are not fully understood. Based on observations, production of CH3I via photochemical degradation of organic material or via phytoplankton production has been proposed. Additional insights could not be gained from correlations between observed biological and environmental variables or from biogeochemical modeling to identify unambiguously the source of methyl iodide. In this study, we aim to address this question of source mechanisms with a three-dimensional global ocean general circulation model including biogeochemistry (MPIOM-HAMOCC (MPIOM - Max Planck Institute Ocean Model HAMOCC - HAMburg Ocean Carbon Cycle model)) by carrying out a series of sensitivity experiments. The simulated fields are compared with a newly available global data set. Simulated distribution patterns and emissions of CH3I differ largely for the two different production pathways. The evaluation of our model results with observations shows that, on the global scale, observed surface concentrations of CH3I can be best explained by the photochemical production pathway. Our results further emphasize that correlations between CH3I and abiotic or biotic factors do not necessarily provide meaningful insights concerning the source of origin. Overall, we find a net global annual CH3I air-sea flux that ranges between 70 and 260 Gg yr-1. On the global scale, the ocean acts as a net source of methyl iodide for the atmosphere, though in some regions in boreal winter, fluxes are of the opposite direction (from the atmosphere to the ocean).

  8. 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

  9. Antifungal Activity of Ag(I) and Zn(II) Complexes of Sulfacetamide Derivatives

    PubMed Central

    Supuran, Claudiu T.

    2000-01-01

    Reaction of sulfacetamide with arylsulfonyl isocyanates afforded a series of derivatives which were used as ligands (as conjugate bases) for the preparation of metal complexes containing Ag(I) and Zn(II). The newly synthesized complexes, unlike the free ligands, act as effective antifungal agents against Aspergillus and Candida spp., some of them showing activities comparable to ketoconazole, with minimum inhibitory concentrations in the range of 0.3 – 0.5 μg/mL. The mechanism of antifungal action of these complexes seems to be not connected with the inhibition of lanosterol-14-α-demethylase, since the levels of sterols assessed in the fungi cultures were equal in the absence or in the presence of the tested compounds. Probably the new complexes act as inhibitors of phosphomannose isomerase, a key enzyme in the biosynthesis of yeast cell walls. PMID:18475922

  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. 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

  12. 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.

  13. 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.

  14. 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

  15. 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.

  16. 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.

  17. 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.

  18. 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.

  19. 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

  20. 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.

  1. 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.

  2. 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

  3. 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

  4. Trigonal prismatic Cu(I) and Ag(I) pyrazolato nanocage hosts: encapsulation of S8 and hydrocarbon guests.

    PubMed

    Duan, Peng-Cheng; Wang, Zhao-Yang; Chen, Jing-Huo; Yang, Guang; Raptis, Raphael G

    2013-11-14

    Two neutral hexanuclear trigonal prismatic cage molecules have been synthesized by coupling two planar triangular M3pz3-panels, M = Cu(I) and Ag(I), in eclipsed geometry. The ~230 Å(3) cage volume can be either vacant or occupied by neutral guests. The crystal structures of the M6-cyclohexane and Ag6-S8 host-guest species have been determined.

  5. Phase stability and electronic properties of silver halides

    NASA Astrophysics Data System (ADS)

    Boukhtouta, M.; Lamraoui, S.; Touam, S.; Meradji, H.; Ghemid, S.; El Haj Hassan, F.

    2015-04-01

    In this work, we study the phase stability and electronic properties of silver halides ( AgBr, AgCl and AgI) using the full-potential linearized augmented plane wave method within the density functional theory. In this approach, the Wu-Cohen generalized gradient approximation was used for the exchange-correlation potential. Moreover, the modified Becke-Johnson approximation was also used for band-structure calculations. Various structural phase transitions were considered here in order to confirm the most stable structure and to predict the phase transition under hydrostatic pressure. In addition, we have studied the band structures of the stable phases of these compounds which reveal that the three compounds exhibit semiconducting behavior. The results obtained are compared with other calculations and experimental measurements.

  6. 21 CFR 520.763 - Dithiazanine iodide oral dosage forms.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Dithiazanine iodide oral dosage forms. 520.763... (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS ORAL DOSAGE FORM NEW ANIMAL DRUGS § 520.763 Dithiazanine iodide oral dosage forms....

  7. 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... (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS ORAL DOSAGE FORM NEW ANIMAL DRUGS § 520.763 Dithiazanine iodide oral dosage forms....

  8. 21 CFR 520.763 - Dithiazanine iodide oral dosage forms.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Dithiazanine iodide oral dosage forms. 520.763... (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS ORAL DOSAGE FORM NEW ANIMAL DRUGS § 520.763 Dithiazanine iodide oral dosage forms....

  9. 21 CFR 520.763 - Dithiazanine iodide oral dosage forms.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Dithiazanine iodide oral dosage forms. 520.763... (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS ORAL DOSAGE FORM NEW ANIMAL DRUGS § 520.763 Dithiazanine iodide oral dosage forms....

  10. 21 CFR 520.763 - Dithiazanine iodide oral dosage forms.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Dithiazanine iodide oral dosage forms. 520.763... (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS ORAL DOSAGE FORM NEW ANIMAL DRUGS § 520.763 Dithiazanine iodide oral dosage forms....

  11. Selective and sensitive optical chemosensor for detection of Ag(I) ions based on 2(4-hydroxy pent-3-en-2-ylideneamine) phenol in aqueous samples.

    PubMed

    Mirzaei, Mohammad; Saeed, Jaber

    2011-11-01

    A selective and sensitive chemosensor, based on the 2(4-hydroxy pent-3-en-2-ylideneamine) phenol (HPYAP) as chromophore, has been developed for colorimetric and visual detection of Ag(I) ions. HPYAP shows a considerable chromogenic behavior toward Ag(I) ions by changing the color of the solution from pale-yellow to very chromatic-yellow, which can be easily detected with the naked-eye. The chemosensor exhibited selective absorbance enhancement to Ag(I) ions in water samples over other metal ions at 438 nm, with a linear range of 0.4-500 μM (r(2)=0.999) and a limit of detection 0.07 μM of Ag(I) ions with UV-vis spectrophotometer detection. The relative standard deviation (RSD) for 100 μM Ag(I) ions was 2.05% (n=7). The proposed method was applied for the determination Ag(I) ions in water and waste water samples.

  12. Selective and sensitive optical chemosensor for detection of Ag(I) ions based on 2(4-hydroxy pent-3-en-2-ylideneamine) phenol in aqueous samples

    NASA Astrophysics Data System (ADS)

    Mirzaei, Mohammad; Saeed, Jaber

    2011-11-01

    A selective and sensitive chemosensor, based on the 2(4-hydroxy pent-3-en-2-ylideneamine) phenol (HPYAP) as chromophore, has been developed for colorimetric and visual detection of Ag(I) ions. HPYAP shows a considerable chromogenic behavior toward Ag(I) ions by changing the color of the solution from pale-yellow to very chromatic-yellow, which can be easily detected with the naked-eye. The chemosensor exhibited selective absorbance enhancement to Ag(I) ions in water samples over other metal ions at 438 nm, with a linear range of 0.4-500 μM ( r2 = 0.999) and a limit of detection 0.07 μM of Ag(I) ions with UV-vis spectrophotometer detection. The relative standard deviation (RSD) for 100 μM Ag(I) ions was 2.05% ( n = 7). The proposed method was applied for the determination Ag(I) ions in water and waste water samples.

  13. 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.

  14. The Advanced Gamma-ray Imaging System (AGIS): Schwarzschild-Couder (SC) Telescope Mechanical and Optical System Design

    NASA Astrophysics Data System (ADS)

    Guarino, V.; Vassiliev, V.; Buckley, J.; Byrum, K.; Falcone, A.; Fegan, S.; Finley, J.; Hanna, D.; Kaaret, P.; Konopelko, A.; Krawczynski, H.; Krennrich, F.; Romani, R.; Wagner, R.; Woods, M.

    2009-05-01

    The concept of a future ground-based gamma-ray observatory, AGIS, in the energy range 20 GeV to 200 TeV is based on an array of 50-100 imaging atmospheric Cherenkov telescopes (IACTs). The anticipated improvement of AGIS sensitivity, angular resolution, and reliability of operation imposes demanding technological and cost requirements on the design of IACTs. In this submission, we focus on the optical and mechanical systems for a novel Schwarzschild-Couder two-mirror aplanatic optical system originally proposed by Schwarzschild. Emerging new mirror production technologies based on replication processes, such as cold and hot glass slumping, cured CFRP, and electroforming, provide new opportunities for cost effective solutions for the design of the optical system. We explore capabilities of these mirror fabrication methods for the AGIS project and alignment methods for optical systems. We also study a mechanical structure which will provide support points for mirrors and camera design driven by the requirement of minimizing the deflections of the mirror support structures.

  15. Photoelectron spectroscopy of AgCl, AgBr, and AgI vapors

    SciTech Connect

    Berkowitz, J.; Batson, C.H.; Goodman, G.L.

    1980-06-01

    He I photoelectron spectra of AgCl, AgBr and AgI vapors have been obtained which differ significantly from earlier work. In each instance, the characteristic features of the diatomic molecule are prominent. The spectral features separate into a valence region, predominantly halogen p-like, and a deeper region, predominantly of Ag 4d character. The latter is split by spin--orbit and ligand field interactions, which are parametrized from the experimental data. Relativistic calculations of the X/sub ..cap alpha../--DVM--SCC type have been performed for these species. At the transition state level, they agree very well with the experimental peak positions. Nonrelativistic calculations of this type have been performed for CuCl and cyclic Cu/sub 3/Cl/sub 3/. Unlike the AgX species, the CuCl and Cu/sub 3/Cl/sub 3/ exhibit strong mixing of metal d and halogen p orbitals for the uppermost occupied orbital, and other Cu 3d-like orbitals above the Cl 3p-like orbitals. It is suggested that the occurrence of Cu 3d orbitals in the valence region may play a role in the anomalous diagmagnetic signal and large conductivity changes of CuCl condensed from the vapor.

  16. 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.

  17. The truth about silver.

    PubMed

    Ovington, Liza G

    2004-09-01

    Interest in silver as a topical agent in wound healing is undergoing a renaissance. Having basic information regarding silver's chemical properties and potential actions in the wound bed is important to its appropriate clinical use. Such information is also relevant to the interpretation of silver's in vitro antimicrobial (antiseptic) effects, which in turn relate to issues involved in the evaluation of the clinical effects of silver in vivo. Gaining an understanding of the basic science of silver products and the different challenges inherent to in vitro versus in vivo antimicrobial evaluations will allow clinicians to address several key questions inherent when considering the use of silver as a topical antimicrobial: 1) Are there different forms of silver? 2) How does the amount of silver released into the wound environment correlate with clinical benefit? 3) How does the rate of silver release correlate with clinical benefit?

  18. Kinetic-spectrophotometric determination of trace amounts of silver using the oxidation of thionine with peroxodisulfate.

    PubMed

    Tabatabaee, Masoumeh; Nateghi, Mohamad R; Mosavi, Seyed Jaml

    2006-12-01

    A simple, rapid and sensitive method has been developed for determination of traces of silver(I) (0.2 - 13 ng mL(-1)) based on its catalytic effect on the oxidation of thionine by peroxodisulfate in the presence of 1 - 10 phenanthroline as an activator. The reaction is monitored spectrophotometrically by measuring the decrease in absorbance of thionine at 600 nm by the fixed time method. The detection limit is 0.098 ng mL(-1) and the relative standard deviation for 0.5, 3.0, 5.0 and 10 ng ml(-1) Ag(I) are 4.1, 1.37, 1.06 and 0.64%, respectively. The method is free from most interferences and it was applied to determination of silver in photographic solutions and well-water samples.

  19. Synthesis of Peptides by Silver-Promoted Coupling of Carboxylates and Thioamides: Mechanistic Insight from Computational Studies.

    PubMed

    Hutton, Craig A; Shang, Jing; Wille, Uta

    2016-02-24

    The mechanism of the recently described N→C direction peptide synthesis through silver-promoted coupling of N-protected amino acids with thioacetylated amino esters was explored by using density functional theory. Calculation of the potential energy surfaces for various pathways revealed that the reaction proceeds through silver-assisted addition of the carboxylate to the thioamide, which is followed by deprotonation and silver-mediated extrusion of sulfur as Ag2 S. The resulting isoimide is the key intermediate, which subsequently rearranges to an imide through a concerted pericyclic [1,3]-acyl shift (O-sp(2) N 1,3-acyl migration). The proposed mechanism clearly emphasises the requirement of two equivalents of Ag(I) and basic reaction conditions, which is in full agreement with the experimental findings. Alternative rearrangement pathways involving only one equivalent of Ag(I) or through O-sp(3) N 1,3-acyl migration can be excluded. The computations further revealed that peptide couplings involving thioformamides require significant conformational changes in the intermediate isoformimide, which slow down the rearrangement process. PMID:26813415

  20. The distribution of iodide at the sea surface.

    PubMed

    Chance, Rosie; Baker, Alex R; Carpenter, Lucy; Jickells, Tim D

    2014-08-01

    Recent studies have highlighted the impact of sea surface iodide concentrations on the deposition of ozone to the sea surface and the sea to air flux of reactive iodine. The use of models to predict this flux demands accurate, spatially distributed sea surface iodide concentrations, but to date, the observational data required to support this is sparse and mostly arises from independent studies conducted on small geographical and temporal scales. We have compiled the available measurements of sea surface iodide to produce a data set spanning latitudes from 69°S to 66°N, which reveals a coherent, large scale distribution pattern, with highest concentrations observed in tropical waters. Relationships between iodide concentration and more readily available parameters (chlorophyll, nitrate, sea surface temperature, salinity, mixed layer depth) are evaluated as tools to predict iodide concentration. Of the variables tested, sea surface temperature is the strongest predictor of iodide concentration. Nitrate was also strongly inversely associated with iodide concentration, but chlorophyll-a was not.

  1. Metallophilicity-driven dynamic aggregation of a phosphorescent gold(I)-silver(I) cluster prepared by solution-based and mechanochemical approaches.

    PubMed

    Ni, Wen-Xiu; Qiu, Yu-Min; Li, Mian; Zheng, Ji; Sun, Raymond Wai-Yin; Zhan, Shun-Ze; Ng, Seik Weng; Li, Dan

    2014-07-01

    We observed an unusual reversible aggregation process showing stimuli-responsive structural dynamics and optical changes attributed to the formation of a sandwich-like Au3-Ag-Au3 cluster, which can be synthesized through both solution and mechanochemical methods. Unlike many other heteronuclear gold-silver clusters, the affinity of two cyclic Au3 complexes and a Ag(I) ion is solely bound by ligand unsupported Au-Ag bonding. The assembly/disassembly behavior, further forming nanoaggregates, is controllable by adjusting the concentration of the solution. In the solid state, the insertion of Ag(I) ion can be implemented through a mechanochemical approach, accompanied by visual color changes and reversible luminochromism. Furthermore, an uncommon solid-liquid extraction is demonstrated, showing the uniqueness of this labile Au-Ag metallophilicity and hinting at the possibility of manipulating a bonding process through a heterogeneous route.

  2. Iodide-mediated control of rhodium epitaxial growth on well-defined noble metal nanocrystals: synthesis, characterization, and structure-dependent catalytic properties.

    PubMed

    Sneed, Brian T; Kuo, Chun-Hong; Brodsky, Casey N; Tsung, Chia-Kuang

    2012-11-01

    Metal nanocrystals (NCs) comprising rhodium are heterogeneous catalysts for CO oxidation, NO reduction, hydrogenations, electro-oxidations, and hydroformylation reactions. It has been demonstrated that control of structure at the nanoscale can enhance the performance of a heterogeneous metal catalyst, such as Rh, but molecular-level control of NCs comprising this metal is less studied compared to gold, silver, platinum, and palladium. We report an iodide-mediated epitaxial overgrowth of Rh by using the surfaces of well-defined foreign metal crystals as substrates to direct the Rh surface structures. The epigrowth can be accomplished on different sizes, morphologies, and identities of metal substrates. The surface structures of the resulting bimetallic NCs were studied using electron microscopy, and their distinct catalytic behaviors were examined in CO stripping and the electro-oxidation of formic acid. Iodide was found to play a crucial role in the overgrowth mechanism. With the addition of iodide, the Rh epigrowth can even be achieved on gold substrates despite the rather large lattice mismatch of ~7%. Hollow Rh nanostructures have also been generated by selective etching of the core substrates. The new role of iodide in the overgrowth and the high level of control for Rh could hold the key to future nanoscale control of this important metal's architecture for use in heterogeneous catalysis.

  3. 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.

  4. Reaction of N-sulfonyltellurimides with methyl iodide

    SciTech Connect

    Naddaka, V.I.; Avanesyan, K.V.; Cherkinskaya, M.L.; Minkin, V.I.

    1987-09-20

    While developing researches into the reactivity of tellurimides, the authors studied the previously unknown reaction of N-sulonyltellurimides with methyl iodide. The authors established that bis(diphenyltellurium) oxide and N-methyl-p-toluenesulfonamide are formed when the tellurimide is boiled in methyl iodide. Such a direction is evidently due to the fact that the telluronium salt produced during the reaction is readily hydrolyzed at the Te-N bond on account of the presence of traces of moisture in the methyl iodide. However, the heating of the tellurimides with an excess of anhydrous methyl iodide in a sealed tube leads to diaryltellurium diiodides and N,N-dimethylsulfonamides. The PMR spectra of solutions of the substances in deuterochloroform were recorded on a Tesla-BS-487 spectrometer at 80 MHz with HMDS as internal standard. The IR spectra were obtained on a Specord 71-IR instrument in Vaseline oil.

  5. 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.

  6. First principle study of 0.75AgI:0.25AgCl: A density functional approach

    NASA Astrophysics Data System (ADS)

    Rao, B. Keshav; Verma, Mohan L.

    2016-09-01

    The first principles calculations based on norm-conserving pseudo potentials and density functional theory are performed for zincblende structured new host 0.75AgI:0.25AgCl. For comparison point of view zincblende structured β-AgI is considered. The structural analysis provides the higher cationic concentration in new host. Density of state analysis explains a weak p-d hybridization in β-AgI and strong in new host. There is decrease in forbidden energy band gap by 0.05 eV and hence large ionic concentration and conductivity is found in new host.

  7. Nanochemistry: Iron cluster reactions with methyl iodide

    SciTech Connect

    McCarter, B.E.; Bililign, S.; Feigerle, C.S.; Miller, J.C.

    1999-08-26

    Previous experiments have shown that the ionization/dissociation of iron pentacarbonyl clusters can lead to the formation of iron ions and iron cluster ions that that these species can further react with dopant molecules to yield chemically rearranged products. The present experiments characterize similar reactions with methyl iodide molecules and clusters. Heteroclusters of the form [Fe(CO){sub 5}]{sub m}(CH{sub 3}I){sub n}Ar{sub p} are created in an expanding supersonic jet of the component molecules. Following ionization by a 30 ps, 266 nm laser pulse, extensive dissociation, aggregation, and chemical rearrangement occur leading to ionic products, which are characterized by mass spectrometry. Cluster ions of the type Fe{sub m}I{sub n}{sup +}, Fe(CH{sub 3}I){sub n}{sup +} are observed as products. The stability of the binary parent ion Fe(CH{sub 3}I){sup +} is demonstrated for the first time.

  8. Chloride, bromide and iodide scintillators with europium

    DOEpatents

    Zhuravleva, Mariya; Yang, Kan

    2016-09-27

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

  9. 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

  10. 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 ...

  11. 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.

  12. 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.

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

    NASA Astrophysics Data System (ADS)

    Shirzaditabar, Farzad; Saliminasab, Maryam

    2013-08-01

    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.

  14. 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.

  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. 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

  17. 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.

  18. 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

  19. Determination of trace silver by solid substrate-room temperature phosphorescence quenching method based on double catalytic system of meta-nitrophenyfluorone-polyoxyethylene-chromium-potassium bromate-β-cyclodextrin

    NASA Astrophysics Data System (ADS)

    Jiaming, Liu; Xuan, Lin; Aihong, Wu; Li-Xiang, Hu; Hangxia, HE; Honghua, Huang; Longdi, Li; Shaoqin, Lin

    2006-09-01

    A new solid substrate-room temperature phosphorescence (SS-RTP) quenching method for the determination of trace silver has been established. It is based on the fact that when using Mg 2+ as ion perturber and β-CD as surfactant, the system of meta-nitrophenyfluorone (R)-polyoxyethylene-Cr(III) can emit strong and stable room temperature phosphorescence signal on filter paper whose surface is modified by polyvinyl alcohol (PVA)-H 3BO 3-NaOH. Ag(I) can catalyze KBrO 3 oxidizing R-PEO-Cr(III) system which causes the quenching of SS-RTP. The reducing value of phosphorescence intensity (Δ Ip) is directly proportional to the concentration of Ag(I) in the range of 3.2-160 ag spot -1 (corresponding concentration: 2.43 fg ml -1, the sample volume: 0.40 μl spot -1) with a detection limit (LD) of 0.97 ag spot -1. The regression equation of working curve can be expressed as Δ Ip = 13.92 + 0.3089 m (ag spot -1) ( r = 0.9983, n = 6). This method has many advantages, such as a wide linear dynamic range, high sensitivity, good repeatability and selectivity. It has been applied to the determination of trace silver in real samples with satisfactory results. What is more, the mechanism of SS-RTP quenching method based on Ag(I) catalyzing KBrO 3 oxidizing meta-nitrophenyfluorone has also been discussed.

  20. 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 ...

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

    NASA Astrophysics Data System (ADS)

    Sidawi, Ibrahim M. S.

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

  3. A Silver Opportunity.

    ERIC Educational Resources Information Center

    Desser, Debra M.

    1996-01-01

    Presents an assignment that involves forming student companies to determine and defend cost estimates for producing a silver Oscar statuette. Includes an assessment rubric for cooperative effort. (JRH)

  4. 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.

  5. The Advanced Glaucoma Intervention Study (AGIS): 10. Variability among academic glaucoma subspecialists in assessing optic disc notching.

    PubMed Central

    Gaasterland, D E; Blackwell, B; Dally, L G; Caprioli, J; Katz, L J; Ederer, F

    2001-01-01

    PURPOSE: An analysis of data from the Advanced Glaucoma Intervention Study (AGIS) has found eyes reported to have partial optic disc rim notching (not to the edge) at baseline to have less risk of subsequent visual field loss than eyes with no notching. Because this is counterintuitive and because classification of notching had not been defined in the AGIS protocol, we have assessed AGIS ophthalmologists interobserver and intraobserver agreement on notching. METHODS: Fourteen glaucoma subspecialists classified notching in 26 pairs of stereoscopic disc photographs of eyes with mild to severe glaucomatous optic neuropathy. They classified images as showing either no notching, notching not to the edge, or notching to the edge. Several hours later, 10 of them classified the same images a second time. RESULTS: In an analysis of interobserver agreement, of 26 stereoscopic images, a plurality of ophthalmologists classified notching as absent in 9 (35%), as present but not to the edge in 7 (27%), and as present and not to the edge in 10 (38%). All 14 ophthalmologists (100%) agreed on the classification of 7 (27%) of the images, and 13 of the 14 ophthalmologists (93%) agreed on the classification of 4 additional images (15%). Of these 11 images with at least 93% agreement, notching was reported as absent in 3 (27%) and to the edge in 8 (73%). In the remaining 15 images, there was substantial disagreement about whether notching was present and, if so, whether it was to the edge. In an analysis of intraobserver agreement, none of the 10 ophthalmologists who completed the viewing a second time classified all eyes exactly the same as the first time, though 5 ophthalmologists made 4 or fewer reclassifications. Overall, 80% of the original classifications were reproduced on second reading. Of the initial classifications that were not reproduced, slightly more than half were first classified as having notching not to the edge. CONCLUSION: Without definitions or examples of optic

  6. 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.

  7. 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

  8. Structure Determination of an Ag(I) -Mediated Cytosine-Cytosine Base Pair within DNA Duplex in Solution with (1) H/(15) N/(109) Ag NMR Spectroscopy.

    PubMed

    Dairaku, Takenori; Furuita, Kyoko; Sato, Hajime; Šebera, Jakub; Nakashima, Katsuyuki; Kondo, Jiro; Yamanaka, Daichi; Kondo, Yoshinori; Okamoto, Itaru; Ono, Akira; Sychrovský, Vladimír; Kojima, Chojiro; Tanaka, Yoshiyuki

    2016-09-01

    The structure of an Ag(I) -mediated cytosine-cytosine base pair, C-Ag(I) -C, was determined with NMR spectroscopy in solution. The observation of 1-bond (15) N-(109) Ag J-coupling ((1) J((15) N,(109) Ag): 83 and 84 Hz) recorded within the C-Ag(I) -C base pair evidenced the N3-Ag(I) -N3 linkage in C-Ag(I) -C. The triplet resonances of the N4 atoms in C-Ag(I) -C demonstrated that each exocyclic N4 atom exists as an amino group (-NH2 ), and any isomerization and/or N4-Ag(I) bonding can be excluded. The 3D structure of Ag(I) -DNA complex determined with NOEs was classified as a B-form conformation with a notable propeller twist of C-Ag(I) -C (-18.3±3.0°). The (109) Ag NMR chemical shift of C-Ag(I) -C was recorded for cytidine/Ag(I) complex (δ((109) Ag): 442 ppm) to completed full NMR characterization of the metal linkage. The structural interpretation of NMR data with quantum mechanical calculations corroborated the structure of the C-Ag(I) -C base pair. PMID:27505707

  9. Structure Determination of an Ag(I) -Mediated Cytosine-Cytosine Base Pair within DNA Duplex in Solution with (1) H/(15) N/(109) Ag NMR Spectroscopy.

    PubMed

    Dairaku, Takenori; Furuita, Kyoko; Sato, Hajime; Šebera, Jakub; Nakashima, Katsuyuki; Kondo, Jiro; Yamanaka, Daichi; Kondo, Yoshinori; Okamoto, Itaru; Ono, Akira; Sychrovský, Vladimír; Kojima, Chojiro; Tanaka, Yoshiyuki

    2016-09-01

    The structure of an Ag(I) -mediated cytosine-cytosine base pair, C-Ag(I) -C, was determined with NMR spectroscopy in solution. The observation of 1-bond (15) N-(109) Ag J-coupling ((1) J((15) N,(109) Ag): 83 and 84 Hz) recorded within the C-Ag(I) -C base pair evidenced the N3-Ag(I) -N3 linkage in C-Ag(I) -C. The triplet resonances of the N4 atoms in C-Ag(I) -C demonstrated that each exocyclic N4 atom exists as an amino group (-NH2 ), and any isomerization and/or N4-Ag(I) bonding can be excluded. The 3D structure of Ag(I) -DNA complex determined with NOEs was classified as a B-form conformation with a notable propeller twist of C-Ag(I) -C (-18.3±3.0°). The (109) Ag NMR chemical shift of C-Ag(I) -C was recorded for cytidine/Ag(I) complex (δ((109) Ag): 442 ppm) to completed full NMR characterization of the metal linkage. The structural interpretation of NMR data with quantum mechanical calculations corroborated the structure of the C-Ag(I) -C base pair.

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

    PubMed Central

    Voigtritter, Karl; Ghorai, Subir

    2011-01-01

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

  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. 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.

  13. A novel three-dimensional AgI coordination polymer based on mixed naphthalene-1,5-disulfonate and aminoacetate ligands.

    PubMed

    Wu, Hua; Lü, Xiao-Li; Lü, Bo; Dong, Chang-Xun; Wu, Mei-Sheng

    2013-08-01

    The three-dimensional coordination polymer poly[[bis(μ₃-2-aminoacetato)di-μ-aqua-μ₃-(naphthalene-1,5-disulfonato)-hexasilver(I)] dihydrate], {[Ag₆(C₁₀H₆O₆S₂)(C₂H₄NO₂)₄(H₂O)₂]·2H₂O}n, based on mixed naphthalene-1,5-disulfonate (L1) and 2-aminoacetate (L2) ligands, contains two Ag(I) centres (Ag1 and Ag4) in general positions, and another two (Ag2 and Ag3) on inversion centres. Ag1 is five-coordinated by three O atoms from one L1 anion, one L2 anion and one water molecule, one N atom from one L2 anion and one AgI cation in a distorted trigonal-bipyramidal coordination geometry. Ag2 is surrounded by four O atoms from two L2 anions and two water molecules, and two AgI cations in a slightly octahedral coordination geometry. Ag3 is four-coordinated by two O atoms from two L2 anions and two AgI cations in a slightly distorted square geometry, while Ag4 is also four-coordinated by two O atoms from one L1 and one L2 ligand, one N atom from another L2 anion, and one AgI cation, exhibiting a distorted tetrahedral coordination geometry. In the crystal structure, there are two one-dimensional chains nearly perpendicular to one another (interchain angle = 87.0°). The chains are connected by water molecules to give a two-dimensional layer, and the layers are further bridged by L1 anions to generate a novel three-dimensional framework. Moreover, hydrogen-bonding interactions consolidate the network.

  14. 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.

  15. 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…

  16. 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

  17. Method for the recovery of silver from silver zeolite

    DOEpatents

    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.

  18. 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.

  19. 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.

  20. 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...

  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; 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 ...

  2. 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...

  3. 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...

  4. 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...

  5. 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...

  6. Palladium-catalyzed direct C-H arylation of cyclic enaminones with aryl iodides.

    PubMed

    Yu, Yi-Yun; Bi, Lei; Georg, Gunda I

    2013-06-21

    A ligand-free method for the Pd-catalyzed direct arylation of cyclic enaminones using aryl iodides was developed. This method can be applied to a wide range of cyclic enaminones and aryl iodides with excellent C5-regioselectivity. Using widely available aryl iodides, the generality of this transformation provides easy access to a variety of 3-arylpiperidine structural motifs.

  7. 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...

  8. 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.…

  9. 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

  10. High Pressure Electrochemistry: Application to silver halides

    NASA Astrophysics Data System (ADS)

    Havens, K.; Kavner, A.

    2007-12-01

    Electron and ion charge transfer processes help govern electrical conductivity and diffusive mass and heat transport properties in deep Earth minerals. In an attempt to understand how pressure influences charge transfer behavior, the halide silver bromide (AgBr) was studied under the influence of an electric potential difference applied across two electrodes in a diamond anvil cell. This study follows our previous work on AgI, which was found to dissociate to molecular iodine and silver metal due to pressure and voltage influences. We performed two sets of experiments on AgBr at high pressure in a diamond anvil cell: electrochemical dissociation and electrical resistance measurements. In our study, we were able to electrochemically dissociate AgBr at pressures of 0.25-1.6 GPa by applying a voltage across the electrodes in the diamond cell sample chamber. Ag metal grew visibly on the negatively-charged electrode when voltages varying from 0.1 V to 5 V were applied. Additionally, a dark blue color appeared in low pressure areas of the diamond cell and grew darker from both voltage application and light exposure, indicating photochemical effects. We found that the reaction area and growth rate of both metal and dark blue color strongly increased as voltage increased, but tended to decrease with greater pressure. The resistance across the cell was observed to be influenced by both pressure and light exposure. As the AgBr sample was exposed to visible light, the resistance dropped instantaneously, and after the light was turned off, the resistance increased on a timescale of 10's of seconds to minutes. Notably, at higher pressures, the AgBr showed less photosensitivity. Exploration of these metal halide systems has many potential applications. First, these experiments explore the pressure-dependence of photochemical and photovoltaic processes, and may spur development of pressure-tuned microscale electronic devices. Second, these experimental results can be used to

  11. 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

  12. 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

  13. (Aminophosphane)gold(I) and silver(I) complexes as antibacterial agents.

    PubMed

    Ortego, Lourdes; Gonzalo-Asensio, Jesús; Laguna, Antonio; Villacampa, M Dolores; Gimeno, M Concepción

    2015-05-01

    This manuscript describes the synthesis of new Au(I) and Ag(I) complexes with aminophosphane ligands and a study of their antibacterial activity against Gram-negative Salmonella enterica serovar typhimurium and Escherichia coli and Gram-positive Listeria monocytogenes and Staphylococcus aureus. The bactericidal assays revealed the effectiveness of these compounds on paradigm Gram-negative and Gram-positive pathogens, showing a moderate antimicrobial activity, comparable with the antibiotics of reference, for all gold(I) complexes and the silver(I) complexes without coordinated PPh3 groups. For those complexes that were found to show inhibitory activity, serial dilutions in liquid broth method were performed for determination of MIC (minimum inhibitory concentration) and MBC (minimum bactericidal concentration).

  14. 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

  15. Crystal structure of catena-poly[silver(I)-μ-l-tyrosinato-κ2 O:N

    PubMed Central

    Yousaf, Aqsa; Tahir, Muhammad Nawaz; Rauf, Abdul; Awan, Shafique Ahmad; Ahmad, Saeed

    2015-01-01

    The title compound, [Ag(C9H10NO3)]n, is a polymeric silver(I) complex of l-tyrosine. The AgI atom is connected to N and O atoms of two different l-tyrosine ligands in an almost linear arrangement, with an Ni—Ag—O1 bond angle of 173.4 (2)° [symmetry code: (i) x + 1, y, z]. The Ag—Ni and Ag—O bond lengths are 2.156 (5) and 2.162 (4) Å, respectively. The polymeric chains extend along the crystallographic a axis. Strong hydrogen bonds of the N—H⋯O and O—H⋯O types and additional C—H⋯O inter­actions connect these chains into a double-layer polymeric network in the ab plane. PMID:25844203

  16. Crystal structure of catena-poly[silver(I)-μ-l-tyrosinato-κ(2) O:N].

    PubMed

    Yousaf, Aqsa; Tahir, Muhammad Nawaz; Rauf, Abdul; Awan, Shafique Ahmad; Ahmad, Saeed

    2015-03-01

    The title compound, [Ag(C9H10NO3)] n , is a polymeric silver(I) complex of l-tyrosine. The Ag(I) atom is connected to N and O atoms of two different l-tyrosine ligands in an almost linear arrangement, with an N(i)-Ag-O1 bond angle of 173.4 (2)° [symmetry code: (i) x + 1, y, z]. The Ag-N(i) and Ag-O bond lengths are 2.156 (5) and 2.162 (4) Å, respectively. The polymeric chains extend along the crystallographic a axis. Strong hydrogen bonds of the N-H⋯O and O-H⋯O types and additional C-H⋯O inter-actions connect these chains into a double-layer polymeric network in the ab plane.

  17. Crystal structure of catena-poly[silver(I)-μ-l-tyrosinato-κ(2) O:N].

    PubMed

    Yousaf, Aqsa; Tahir, Muhammad Nawaz; Rauf, Abdul; Awan, Shafique Ahmad; Ahmad, Saeed

    2015-03-01

    The title compound, [Ag(C9H10NO3)] n , is a polymeric silver(I) complex of l-tyrosine. The Ag(I) atom is connected to N and O atoms of two different l-tyrosine ligands in an almost linear arrangement, with an N(i)-Ag-O1 bond angle of 173.4 (2)° [symmetry code: (i) x + 1, y, z]. The Ag-N(i) and Ag-O bond lengths are 2.156 (5) and 2.162 (4) Å, respectively. The polymeric chains extend along the crystallographic a axis. Strong hydrogen bonds of the N-H⋯O and O-H⋯O types and additional C-H⋯O inter-actions connect these chains into a double-layer polymeric network in the ab plane. PMID:25844203

  18. 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.

  19. Characterization of crystal defects in mixed tabular silver halide grains by conventional transmission electron microscopy and X-ray diffractometry

    NASA Astrophysics Data System (ADS)

    Goessens, C.; Schryvers, D.; Van Landuyt, J.; Amelinckx, S.; Verbeeck, A.; De Keyzer, R.

    1991-04-01

    Tabular silver bromide grains with iodide uniformly mixed in the shell were investigated with conventional transmission electron microscopy. The shell region was found to contain a large number of stacking faults parallel with the {111¯} edges and in some cases edge dislocations with a Burgers vector of 1/2 >[11¯0] type. An atomic model for the formation of the stacking faults during the growth is presented.

  20. 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.

  1. 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.

  2. Synthesis of silver nanoparticles by electron irradiation of silver acetate

    NASA Astrophysics Data System (ADS)

    Li, Yue; Kim, Yong Nam; Lee, Eun Je; Cai, Wei Ping; Cho, Sung Oh

    2006-10-01

    A novel and facile route to synthesize crystalline silver nanoparticles is presented, which is based on electron irradiation technique. Only by irradiating an electron beam onto silver acetate precursor material, silver nanocrystals with the sizes of 15-40 nm were synthesized. The morphology and chemical composition of the irradiated samples were characterized by SEM, TEM, XRD and EELS. The precursor material was decomposed by the energetic electrons and consequently the chemical composition of the material was changed. As the electron fluence was gradually increased, the precursor was converted to silver (I) oxide and finally into silver nanocrystals. Thus, besides silver nanoparticles, silver oxide film can also be synthesized using the electron irradiation technique by controlling the electron fluence. The technique can be useful for mass production of silver nanoparticles and for patterned silver nanoparticle film.

  3. Defective organification of iodide causing congenital goitrous hypothyroidism.

    PubMed

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

    1996-01-01

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

  4. 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.

  5. Give silver a shine.

    PubMed

    Fromm, Katharina M

    2011-02-01

    Katharina M. Fromm explains how, as well as catalysis and jewellery, silver serves a myriad of medicinal applications--some of which are even behind poetic traditions such as throwing coins in wishing wells. PMID:21258393

  6. 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.

  7. Electrochemical behavior of silver sulfide

    SciTech Connect

    Drouven, B.U.E.

    1982-01-01

    The electrochemical behavior of silver sulfide in sulfuric acid as well as in nitric acid was studied using electrodes made from synthetic silver sulfide. The primary techniques used were potentiostatic, potentiodynamic, galvanostatic and corrosion cell experiments. The cathodic reaction of silver sulfide produces silver and hydrogen sulfide. This reaction mechanism is a sequential two step charge transfer involving a single electron in each step. Silver ions are produced from silver sulfide upon applying an anodic potential. The dissolution rate of silver sulfide can be so high that the formation of silver sulfate occurs which partially covers the silver sulfide surface and inhibits a further rate increase. The sulfur from the silver sulfide will be oxidized at low overpotentials to elemental sulfur; at high overpotentials, the oxidation to sulfate or bisulfate is observed. The results suggest that the catalysis of chalcopyrite by the addition of silver ions is caused by the formation and subsequent dissolution of silver sulfide leaving a porous layer behind. The understanding of the reaction mechanism of silver sulfide dissolution and its optimization will significantly improve the economic evaluation of industrial processes using the catalyzed leaching of chalcopyrite. The present knowledge of the catalysis indicates that other ions may be substituted for silver ions which would increase the feasibility of hydrometallurgical processes.

  8. 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.

  9. Effects of Ag(I), Au(III), and Cu(II) on the reductive dechlorination of carbon tetrachloride by green rust.

    PubMed

    O'Loughlin, Edward J; Kemner, Kenneth M; Burris, David R

    2003-07-01

    Green rusts (GRs), mixed iron(II)/iron(III) hydroxide minerals found in many suboxic environments, have been shown to reduce a range of organic and inorganic contaminants, including several chlorinated hydrocarbons. Many studies have demonstrated the catalytic activity of transition metal species in the reduction of chlorinated hydrocarbons, suggesting the potential for enhanced reduction by GR in the presence of an appropriate transition metal catalyst. Reductive dechlorination of carbon tetrachloride (CT) was examined in aqueous suspensions of GR amended with Ag(I), Au(III), or Cu(II). The CT reduction rates were greatly increased for systems amended with Cu(II), Au(III), and Ag(I) (listed in order of increasing rates) relative to GR alone. Observed intermediates and products included chloroform, dichloromethane, chloromethane, methane, acetylene, ethene, ethane, carbon monoxide, tetrachloroethene, and various nonchlorinated C3 and C4 compounds. Product distributions for the reductive dechlorination of CT were highly dependent on the transition metal used. A reaction pathway scheme is proposed in which CT is reduced primarily to methane and other nonchlorinated end products, largely through a series of one-electron reductions forming radicals and carbenes/carbenoids. Recently, X-ray absorption fine structure analysis of aqueous GR suspensions amended with Ag(I), Au(III), or Cu(II) showed that the metals were reduced to their zerovalent forms. A possible mechanism for CT reduction is the formation of a galvanic couple involving the zerovalent metal and GR, with reduction of CT occurring on the surface of the metal and GR serving as the bulk electron source. The enhanced reduction of CT by GR suspensions amended with Ag(I), Au(III), or Cu(II) may prove useful in the development of improved materials for remediation of chlorinated organic contaminants.

  10. Immobilization of Ag(i) into a metal-organic framework with -SO3H sites for highly selective olefin-paraffin separation at room temperature.

    PubMed

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

    2015-02-18

    Introduction of Ag(i) ions into a sulfonic acid functionalized MOF ((Cr)-MIL-101-SO3H) significantly enhances its interactions with olefin double bonds, leading to its much higher selectivities for the separation of C2H4-C2H6 and C3H6-C3H8 at room temperature over the original (Cr)-MIL-101-SO3H and other adsorbents at room temperature.

  11. 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

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

    NASA Astrophysics Data System (ADS)

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

    2006-09-01

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

  13. A Halogen-Bond-Induced Triple Helicate Encapsulates Iodide.

    PubMed

    Massena, Casey J; Wageling, Nicholas B; Decato, Daniel A; Martin Rodriguez, Enrique; Rose, Ariana M; Berryman, Orion B

    2016-09-26

    The self-assembly of higher-order anion helicates in solution remains an elusive goal. Herein, we present the first triple helicate to encapsulate iodide in organic and aqueous media as well as the solid state. The triple helicate self-assembles from three tricationic arylethynyl strands and resembles a tubular anion channel lined with nine halogen bond donors. Eight strong iodine⋅⋅⋅iodide halogen bonds and numerous buried π-surfaces endow the triplex with remarkable stability, even at elevated temperatures. We suggest that the natural rise of a single-strand helix renders its linear halogen-bond donors non-convergent. Thus, the stringent linearity of halogen bonding is a powerful tool for the synthesis of multi-strand anion helicates. PMID:27411932

  14. 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.

  15. 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.

  16. 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.

  17. Structural insight into iodide uptake by AFm phases.

    PubMed

    Aimoz, Laure; Wieland, Erich; Taviot-Guého, Christine; Dähn, Rainer; Vespa, Marika; Churakov, Sergey V

    2012-04-01

    The ability of cement phases carrying positively charged surfaces to retard the mobility of (129)I, present as iodide (I(-)) in groundwater, was investigated in the context of safe disposal of radioactive waste. (125)I sorption experiments on ettringite, hydrotalcite, chloride-, carbonate- and sulfate-containing AFm phases indicated that calcium-monosulfate (AFm-SO(4)) is the only phase that takes up trace levels of iodide. The structures of AFm phases prepared by coprecipitating iodide with other anions were investigated in order to understand this preferential uptake mechanism. X-ray diffraction (XRD) investigations showed a segregation of monoiodide (AFm-I(2)) and Friedel's salt (AFm-Cl(2)) for I-Cl mixtures, whereas interstratifications of AFm-I(2) and hemicarboaluminate (AFm-OH-(CO(3))(0.5)) were observed for the I-CO(3) systems. In contrast, XRD measurements indicated the formation of a solid solution between AFm-I(2) and AFm-SO(4) for the I-SO(4) mixtures. Extended X-ray absorption fine structure spectroscopy showed a modification of the coordination environment of iodine in I-CO(3) and in I-SO(4) samples compared to pure AFm-I(2). This is assumed to be due to the introduction of stacking faults in I-CO(3) samples on one hand and due to the presence of sulfate and associated space-filling water molecules as close neighbors in I-SO(4) samples on the other hand. The formation of a solid solution between AFm-I(2) and AFm-SO(4), with a short-range mixing of iodide and sulfate, implies that AFm-SO(4) bears the potential to retard (129)I. PMID:22376086

  18. 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.

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

    SciTech Connect

    Cross, E.S. . Santa Barbara Operations); Mroz, E.; Olivares, J.A. )

    1993-01-01

    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 will discuss 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.

  20. Photochemical versus biological production of methyl iodide during Meteor 55

    NASA Astrophysics Data System (ADS)

    Richter, U.; Wallace, D.

    2003-04-01

    The flux of methyl iodide from sea to air represents the largest flux of iodine from the ocean to the atmosphere. Surface water concentrations and hence fluxes are particularly high in tropical regions. This flux may be responsible for the enrichment of iodine in the marine aerosol and may contribute to important processes in the marine boundary layer, including particle formation. Methyl iodide is commonly referred to as a biogenic gas, with both macroalgae and phytoplankton identified as important sources. On the other hand experimental and field data have shown the importance of photochemical production that is not necessarily associated directly with biological activity. During the Meteor cruise 55 along 11°N in the tropical Atlantic Ocean, a series of experiments were conducted to examine the biological vs. photochemical production of methyl iodide. A total of eight separate experiments were conducted. Production of CH3I in quartz glass flasks during 24 hour incubations (dark and natural sunlight) was measured under three experimental treatments: untreated seawater, filtered seawater (0.1 um pore size filter to exclude most phytoplankton and bacteria), and seawater that was poisoned with mercuric chloride. There were two clear findings from these experiments: (1) methyl iodide production was significantly higher in all the incubations that were exposed to the light than in the dark incubations; (2) there was no significant difference between CH3I production under the three experimental treatments. These results argue very strongly for the primary importance of photochemical production of CH3I as opposed to biogenic production at least for the tropical open ocean surface waters. Further experiments are required to investigate the reactants involved, their sources, the wavelength and depth dependence of production, etc. as well as (possibly related) sink processes.

  1. 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.

  2. 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.

  3. 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

  4. Corrosion mechanism of cuprous oxide/iodide solar electrochemical cell

    NASA Astrophysics Data System (ADS)

    Tennakone, K.; Gurunnanselage, W.; Dharmaratne, D.; Jayewardena, S. C.

    1982-01-01

    Mechanisms for cuprous oxide corrosion in an iodide solution are investigated in light of the importance of instability effects arising from semiconductor electrode corrosion in solar electrochemical cells. Experiments involved the use of a potassium iodide solution containing a trace of iodine as the redox electrolyte, with a cuprous oxide-coated copper plate as the photocathode and a copper window coated with cupric sulphide as the counterelectrode. Measurement of the time dependence of the short circuit current at constant illumination intensity reveals it to undergo a rapid decay accompanied by the formation of a cuprous iodide-cupric oxide deposit on the photocathode surface. The region surrounding a circular patch of light focussed on the photocathode is found to exhibit CuO and CuI deposits signalling corrosion in the anodic region surrounding the cathodic spot. Measurements of the time dependence of the open circuit voltage furthermore indicate that the saturation voltage decays with time, due to short circuiting in the photocathode between anodic and cathodic regions.

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

    PubMed

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

    2006-08-01

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

  6. 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.

  7. Development of the strontium iodide coded aperture (SICA) instrument

    NASA Astrophysics Data System (ADS)

    Mitchell, Lee J.; Phlips, Bernard F.; Grove, J. Eric; Cordes, Ryan

    2015-08-01

    The work reports on the development of a Strontium Iodide Coded Aperture (SICA) instrument for use in space-based astrophysics, solar physics, and high-energy atmospheric physics. The Naval Research Laboratory is developing a prototype coded aperture imager that will consist of an 8 x 8 array of SrI2:Eu detectors, each read out by a silicon photomultiplier. The array would be used to demonstrate SrI2:Eu detector performance for space-based missions. Europium-doped strontium iodide (SrI2:Eu) detectors have recently become available, and the material is a strong candidate to replace existing detector technology currently used for space-based gamma-ray astrophysics research. The detectors have a typical energy resolution of 3.2% at 662 keV, a significant improvement over the 6.5% energy resolution of thallium-doped sodium iodide. With a density of 4.59 g/cm and a Zeff of 49, SrI2:Eu has a high efficiency for MeV gamma-ray detection. Coupling this with recent improvements in silicon photomultiplier technology (i.e., no bulky photomultiplier tubes) creates high-density, large-area, low-power detector arrays with good energy resolution. Also, the energy resolution of SrI2:Eu makes it ideal for use as the back plane of a Compton telescope.

  8. Iodide mumps following fistulogram in a haemodialysis patient.

    PubMed

    Ghosh, Raktim K; Somasundaram, Mey; Ravakhah, Keyvan

    2016-01-01

    Iodide mumps, or contrast-induced acute sialadenitis, is characterised by rapid, painless enlargement of the salivary glands, following the use of iodinated contrast dye. The underlying mechanism of this adverse reaction is not completely understood. It could be due to an idiosyncratic reaction or related to deposition of iodide in the ductal systems of the salivary glands causing blockage and inflammation. With increasing renal dysfunction, the elimination half-life of the iodine-containing contrast dye gets prolonged. The course of iodine-induced sialadenitis is usually benign, and rapid resolution of symptoms is expected without definite treatment. The symptomatic management includes treatment with a parenteral non-steroidal anti-inflammatory drug (NSAID), steroids and dialysis. However, the role of steroids has been found to be controversial in previously published case reports. Pancreatic mumps and transient thyroid dysfunction were also reported in patients following iodinated contrast administration; the aetiology of this is thought to be similar to iodide-induced sialadenitis. PMID:26838304

  9. [Structure-functional organization of eukaryotic high-affinity copper importer CTR1 determines its ability to transport copper, silver and cisplatin].

    PubMed

    Skvortsov, A N; Zatulovskiĭ, E A; Puchkova, L V

    2012-01-01

    It was shown recently, that high affinity Cu(I) importer eukaryotic protein CTR1 can also transport in vitro abiogenic Ag(I) ions and anticancer drug cisplatin. At present there is no rational explanation how CTR1 can transfer platinum group, which is different by coordination properties from highly similar Cu(I) and Ag(I). To understand this phenomenon we analyzed 25 sequences of chordate CTR1 proteins, and found out conserved patterns of organization of N-terminal extracellular part of CTR1 which correspond to initial metal binding. Extracellular copper-binding motifs were qualified by their coordination properties. It was shown that relative position of Met- and His-rich copper-binding motifs in CTR1 predisposes the extracellular CTR1 part to binding of copper, silver and cisplatin. Relation between tissue-specific expression of CTR1 gene, steady-state copper concentration, and silver and platinum accumulation in organs of mice in vivo was analyzed. Significant positive but incomplete correlation exists between these variables. Basing on structural and functional peculiarities of N-terminal part of CTR1 a hypothesis of coupled transport of copper and cisplatin has been suggested, which avoids the disagreement between CTR1-mediated cisplatin transport in vitro, and irreversible binding of platinum to Met-rich peptides.

  10. Laccase-catalyzed oxidation of iodide and formation of organically bound iodine in soils.

    PubMed

    Seki, Miharu; Oikawa, Jun-ichi; Taguchi, Taro; Ohnuki, Toshihiko; Muramatsu, Yasuyuki; Sakamoto, Kazunori; Amachi, Seigo

    2013-01-01

    Laccase oxidizes iodide to molecular iodine or hypoiodous acid, both of which are easily incorporated into natural soil organic matter. In this study, iodide sorption and laccase activity in 2 types of Japanese soil were determined under various experimental conditions to evaluate possible involvement of this enzyme in the sorption of iodide. Batch sorption experiment using radioactive iodide tracer ((125)I(-)) revealed that the sorption was significantly inhibited by autoclaving (121 °C, 40 min), heat treatment (80 and 100 °C, 10 min), γ-irradiation (30 kGy), N(2) gas flushing, and addition of reducing agents and general laccase inhibitors (KCN and NaN(3)). Interestingly, very similar tendency of inhibition was observed in soil laccase activity, which was determined using 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonate) (ABTS) as a substrate. The partition coefficient (K(d): mL g(-1)) for iodide and specific activity of laccase in soils (Unit g(-1)) showed significant positive correlation in both soil samples. Addition of a bacterial laccase with an iodide-oxidizing activity to the soils strongly enhanced the sorption of iodide. Furthermore, the enzyme addition partially restored iodide sorption capacity of the autoclaved soil samples. These results suggest that microbial laccase is involved in iodide sorption on soils through the oxidation of iodide.

  11. 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…

  12. Silver(i) complexes with 1'-(diphenylphosphino)-1-cyanoferrocene: the art of improvisation in coordination.

    PubMed

    Škoch, Karel; Uhlík, Filip; Císařová, Ivana; Štěpnička, Petr

    2016-06-28

    1'-(Diphenylphosphino)-1-cyanoferrocene () reacts with silver(i) halides at a 1 : 1 metal-to-ligand ratio to afford the heterocubane complexes [Ag(μ3-X)(-κP)]4, where X = Cl (), Br (), and I (). In addition, the reaction with AgCl with 2 equiv. of leads to chloride-bridged dimer [(μ-Cl)2{Ag(-κP)2}2] () and, presumably, also to [(μ(P,N)-){AgCl(-κP)}]2 (). While similar reactions with AgCN furnished only the insoluble coordination polymer [(-κP)2Ag(NC)Ag(CN)]n (), those with AgSCN afforded the heterocubane [Ag(-κP)(μ-SCN-S,S,N)]4 () and the thiocyanato-bridged disilver(i) complex [Ag(-κP)2(μ-SCN-S,N)]2 (), thereby resembling reactions in the AgCl- system. Attempted reactions with AgF led to ill-defined products, among which [Ag(-κP)2(μ-HF2)]2 () and [(μ-SiF6){Ag(-κP)2}2] () could be identified. The latter compound was prepared also from Ag2[SiF6] and . Reactions between and AgClO4 or Ag[BF4] afforded disilver complexes [(μ(P,N)-)Ag(ClO4-κO)]2 () and [(μ(P,N)-)Ag(BF4-κF)]2 () featuring pseudolinear Ag(i) centers that are weakly coordinated by the counter anions. A similar reaction with Ag[SbF6] followed by crystallization from ethyl acetate produced an analogous complex, albeit with coordinated solvent, [(μ(P,N)-)Ag(AcOEt-κO)]2[SbF6]2 (). Ultimately, a compound devoid of any additional ligands at the Ag(i) centers, [(μ(P,N)-)Ag]2[B(C6H3(CF3)2-3,5)4]2 (), was obtained from the reaction of with silver(i) tetrakis[3,5-bis(trifluoromethyl)phenyl]borate. The reaction of Ag[BF4] with two equivalents of produced unique coordination polymer [Ag(-κP)(μ(P,N)-)]n[BF4]n (), the structure of which contained one of the phosphinoferrocene ligands coordinated as a P,N-chelate and the other forming a bridge to an adjacent Ag(i) center. All of these compounds were structurally characterized by single-crystal X-ray crystallography, revealing that the lengths of the bonds between silver and its anionic ligand(s) typically exceed the sum of the respective

  13. 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

  14. Palladium-catalyzed Heck-type cross-couplings of unactivated alkyl iodides.

    PubMed

    McMahon, Caitlin M; Alexanian, Erik J

    2014-06-01

    A palladium-catalyzed, intermolecular Heck-type coupling of alkyl iodides and alkenes is described. This process is successful with a variety of primary and secondary unactivated alkyl iodides as reaction partners, including those with hydrogen atoms in the β position. The mild catalytic conditions enable intermolecular C-C bond formations with a diverse set of alkyl iodides and alkenes, including substrates containing base- or nucleophile-sensitive functionality.

  15. Iron-catalyzed 1,2-addition of perfluoroalkyl iodides to alkynes and alkenes.

    PubMed

    Xu, Tao; Cheung, Chi Wai; Hu, Xile

    2014-05-01

    Iron catalysis has been developed for the intermolecular 1,2-addition of perfluoroalkyl iodides to alkynes and alkenes. The catalysis has a wide substrate scope and high functional-group tolerance. A variety of perfluoroalkyl iodides including CF3 I can be employed. The resulting perfluoroalkylated alkyl and alkenyl iodides can be further functionalized by cross-coupling reactions. This methodology provides a straightforward and streamlined access to perfluoroalkylated organic molecules.

  16. Excess iodide decreases transcription of NIS and VEGF genes in rat FRTL-5 thyroid cells

    PubMed Central

    Suzuki, Koichi; Kimura, Hiroaki; Wu, Huhehasi; Kudo, Naoko; Kim, Won Bae; Suzuki, Sayuri; Yoshida, Akio; Caturegli, Patrizio; Kohn, Leonard D.

    2010-01-01

    Although it is well known that an excess of iodide suppresses thyroid function and blood flow in vivo, the underlying molecular mechanisms are not fully known. The functional effect of iodide occurs at multiple steps, which include inhibition of sodium/iodide symporter (NIS) expression, transient block of organification, and inhibition of hormonal release. The vascular effect likely involves suppression of the vascular endothelial growth factor (VEGF) gene. In this report, we show that excess iodide coordinately suppresses the expression of the NIS and VEGF genes in FRTL-5 thyroid cells. We also demonstrate that the mechanism of iodide suppression of NIS gene expression is transcriptional, which is synergized by the addition of thyroglobulin. Based on the findings of reporter gene assays and electrophoretic gel mobility shift analysis, we also report two novel DNA binding proteins that responded specifically to iodide and modulated NIS promoter activity. The results suggest that excess iodide affects thyroid vascular function in addition to iodide uptake. This study provides additional insights into the mechanism of action of excess iodide on thyroid function. PMID:20132794

  17. 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.

  18. Antibacterial Activity and Cytotoxicity of Silver(I) Complexes of Pyridine and (Benz)Imidazole Derivatives. X-ray Crystal Structure of [Ag(2,6-di(CH2OH)py)2]NO3.

    PubMed

    Kalinowska-Lis, Urszula; Felczak, Aleksandra; Chęcińska, Lilianna; Szabłowska-Gadomska, Ilona; Patyna, Emila; Małecki, Maciej; Lisowska, Katarzyna; Ochocki, Justyn

    2016-01-28

    Selected aspects of the biological activity of a series of six nitrate silver(I) complexes with pyridine and (benz)imidazole derivatives were investigated. The present study evaluated the antibacterial activities of the complexes against three Gram-negative strains: Pseudomonas aeruginosa ATCC 15442, Escherichia coli ATCC 25922 and Proteus hauseri ATCC 13315. The results were compared with those of silver nitrate, a silver sulfadiazine drug and appropriate ligands. The most significant antibacterial properties were exerted by silver(I) complexes containing benzimidazole derivatives. The cytotoxic activity of the complexes was examined against B16 (murine melanoma) and 10T1/2 (murine fibroblasts) cells. All of the tested silver(I) compounds were not toxic to fibroblast cells in concentration inhibited cancer cell (B16) viability by 50%, which ranged between 2.44-28.65 µM. The molecular and crystal structure of silver(I) complex of 2,6-di(hydroxymethyl)pyridine was determined by single-crystal X-ray diffraction analysis. The most important features of the crystal packing and intermolecular non-covalent interactions in the Ag(I) complex were quantified via Hirshfeld surface analysis.

  19. Stochastic dynamics of the chlorite-iodide reaction

    NASA Astrophysics Data System (ADS)

    Sagués, F.; Ramírez-Piscina, L.; Sancho, J. M.

    1990-04-01

    A recently proposed theoretical framework appropriate to the study of the stochastic behavior of several chemical systems is used to analyze the irreproducibility of the observed reaction times in the chlorite-iodide clock reaction. Noise terms are incorporated through the kinetic constants and their intensity is further correlated with the inverse of the stirring rate. Analytical and simulation results are obtained for the first moments of the reaction time distribution. These results are compared with recent experimental data obtained by Nagypál and Epstein.

  20. 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.

  1. 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

  2. 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.

  3. 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.

  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. Copper-catalyzed selective arylations of benzoxazoles with aryl iodides.

    PubMed

    Kim, Donghae; Yoo, Kwangho; Kim, Se Eun; Cho, Hee Jin; Lee, Junseong; Kim, Youngjo; Kim, Min

    2015-04-01

    A copper-catalyzed direct ring-opening double N-arylation of benzoxazoles with aryl iodides has been developed. The present system exhibits high selectivity despite competition from C-arylation. The selectivity between ring-opening N-arylation and C-arylation was controlled by the choice of reaction vessel. The nitrile bound bis(triphenylphosphine)copper cyanide was identified as the active catalytic species for both reactions, and when combined with a nitrile-containing solvent, enhanced the reaction efficiency.

  6. 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.

  7. 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.

  8. 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.

  9. 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.

  10. 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

  11. 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…

  12. 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

  13. 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.

  14. Tube-type coordination polymers: two- and four-silver(I)-mediated linear networking of calix[4]arene tetracarboxylates.

    PubMed

    Park, Ki-Min; Lee, Eunji; Park, Chul Soon; Lee, Shim Sung

    2011-12-01

    Two calix[4]arene tetracarboxylates, [calix[4]arene tetraacetate (K(4)CTA) and calix[4]arene tetrabenzoate (K(4)CTB)] as their potassium salts, have been prepared. Employing these as precursors, two Ag(I) coordination polymers incorporating calix[4]arene units have been successfully prepared and their X-ray crystal structures have been determined. In these, the CTA and CTB derivatives are linearly bound to two and four silver atoms, respectively, to generate unusual tubular nanostructures. A comparative NMR study was undertaken to investigate the nature of the metal ion blocking of the tube as observed in the CTA-derived structure. The thermal properties for both coordination polymers were also examined.

  15. 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.

  16. 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.

  17. Synthesis, characterization of Ag(I), Pd(II) and Pt(II) complexes of a triazine-3-thione and their interactions with bovine serum albumin.

    PubMed

    Zhang, Xiuying; Li, Shuyan; Yang, Lin; Fan, Changqing

    2007-11-01

    Ag(I), Pd(II) and Pt(II) complexes of 5-methoxy-5,6-diphenyl-4,5-dihydro-2H-[1,2,4]triazine-3-thione (LH(2)OCH(3)) have been synthesized and characterized by elemental analysis, molar conductance, (1)H NMR, IR spectra, UV spectra and thermal analysis (TG-DTA). The components of the three complexes are [Ag(C(15)H(10)N(3)S)](6), Pd(C(15)H(10)N(3)S)(2) and Pt(C(15)H(10)N(3)S)(2).C(3)H(6)O.2H(2)O, respectively. All the complexes are nonelectrolyte and have high thermodynamic stability. The ligand may act as bidentate NS donor for Pd(II) and Pt(II) complexes, while it seems to be bidentate NS bridging via sulphur atom for Ag(I) complex. A planar quadrangular structure is proposed for Pd(II) and Pt(II) complexes and Ag(I) complex may be a hexanuclear cluster. Their interactions with bovine serum albumin (BSA) are investigated using steady state fluorescence technology. It is observed that all of them can quench the intrinsic fluorescence of BSA through static quenching procedure. The binding constants (K(A)) at different temperatures, thermodynamic parameters enthalpy changes (DeltaH) and entropy changes (DeltaS) between BSA and the compounds are calculated. Based on the values of DeltaH and DeltaS, it is judged that the main acting force of PtL(2).C(3)H(6)O.2H(2)O with BSA may be electrostatic interaction, and for the LH(2)OCH(3), Ag(6)L(6) and PdL(2), hydrophobic and electrostatic interactions may be involved in their binding processes.

  18. Ionic transport in hybrid lead iodide perovskite solar cells

    NASA Astrophysics Data System (ADS)

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

    2015-06-01

    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.

  19. 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

  20. 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.

  1. 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

  2. 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.

  3. Peptide quantitation with methyl iodide isotopic tags and mass spectrometry.

    PubMed

    Blagojevic, Voislav; Zhidkov, Nickholas; Tharmaratnam, Samuel; Pham, Van Thong; Kaplan, Harvey; Bohme, Diethard K

    2010-06-01

    A novel method is presented for the quantitation of peptides based on their methylation by in vacuo chemical reaction with methyl iodide. Samples of two small peptides, hexaglycine and pentaalanine, were labeled with CH(3)I and CD(3)I, representing the "unknown" and "standard" respectively, and then subjected to a series of tests using mass spectrometry to ascertain the suitability of the isotopic labels for peptide quantitation. The experiments show methyl iodide to be a very quantitative label, exhibiting a linear relationship in concentration over the dynamic range of the mass spectrometer used in the analysis (up to 4 orders of magnitude) both as pure samples and in a complex mixture of peptides. The tendency of trimethylated peptides to preferentially form a(2) fragment ions in MS(2) produces a significant increase in sensitivity, especially when the mass spectrometer is used in the MRM mode. Tests were also performed to verify the stability of the label against H/D exchange and its suitability for long-term storage, showing little degradation while in solution and during subsequent chemical processing.

  4. 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).

  5. 21 CFR 73.2500 - Silver.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 1 2014-04-01 2014-04-01 false Silver. 73.2500 Section 73.2500 Food and Drugs... ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2500 Silver. (a) Identity. (1) The color additive, silver, is a crystalline powder of high purity silver prepared by the reaction of silver nitrate with...

  6. 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... ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2500 Silver. (a) Identity. (1) The color additive, silver, is a crystalline powder of high purity silver prepared by the reaction of silver nitrate with...

  7. 21 CFR 73.2500 - Silver.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 1 2012-04-01 2012-04-01 false Silver. 73.2500 Section 73.2500 Food and Drugs... ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2500 Silver. (a) Identity. (1) The color additive, silver, is a crystalline powder of high purity silver prepared by the reaction of silver nitrate with...

  8. 21 CFR 73.2500 - Silver.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 1 2010-04-01 2010-04-01 false Silver. 73.2500 Section 73.2500 Food and Drugs... ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2500 Silver. (a) Identity. (1) The color additive, silver, is a crystalline powder of high purity silver prepared by the reaction of silver nitrate with...

  9. 21 CFR 73.2500 - Silver.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 1 2013-04-01 2013-04-01 false Silver. 73.2500 Section 73.2500 Food and Drugs... ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2500 Silver. (a) Identity. (1) The color additive, silver, is a crystalline powder of high purity silver prepared by the reaction of silver nitrate with...

  10. Structure and spectral properties of the silver-containing high-silica glasses

    NASA Astrophysics Data System (ADS)

    Girsova, M. A.; Golovina, G. F.; Anfimova, I. N.; Arsent'ev, M. Yu; Antropova, T. V.

    2016-08-01

    Silver-containing high-silica glasses were synthesized by an impregnation of the silica porous glasses (PGs) first with AgNO3 aqueous solution (with or without the presence of the sensitizers, such as Cu(NO3)2 or Ce(NO3)3), next in the mixed halide salt (NH4Cl, KBr, KI) solution. Then some part of the samples was sintered at the temperatures from 850 to 900°C up to closing of the pores. The structure of glasses was studied by UV-VIS-NIR and IR spectroscopy and X-ray diffraction (XRD) techniques. According to XRD data the silver-containing high-silica glasses contain the AgBr, AgI, Ag3PO4, (CuBr)0.75(CuI)0.25 phases. IR spectra confirmed B-O-B, Si- O-Si, P-O-P, O-P-O, O-B-O bonds, (PO4)3- and P-O- groups in glasses.

  11. Electrical conductivity of a system of Ag2SO4:AgI eutectic added to 30Li2SO4:70Ag2SO4

    NASA Astrophysics Data System (ADS)

    Chandrayan, V. R.; Tejpal, A.; Singh, K.

    1989-10-01

    The electrical conductivity of rapidly quenched specimens of 48Ag2SO4:52AgI eutectic added to 30Li2SO4:70Ag2SO4 has been measured as a function of frequency and temperature. The results show a significant enhancement in the conductivity of the 30Li2SO4:70Ag2SO4 system with a maximum value at 12.5 mol. pct eutectic. This phenomenon is explained in terms of the dispersive nature of the fine eutectic crystallites in the crystalline matrix of the Li2SO4:Ag2SO4 system.

  12. 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.

  13. 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.

  14. Effects of radiation and temperature on iodide sorption by surfactant-modified bentonite.

    PubMed

    Choung, Sungwook; Kim, Minkyung; Yang, Jung-Seok; Kim, Min-Gyu; Um, Wooyong

    2014-08-19

    Bentonite, which is used as an engineered barrier in geological repositories, is ineffective for sorbing anionic radionuclides because of its negatively charged surface. This study modified raw bentonite using a cationic surfactant (i.e., hexadecyltrimethylammonium [HDTMA]-Br) to improve its sorption capability for radioactive iodide. The effects of temperature and radiation on the iodide sorption of surfactant-modified bentonite (SMB) were also evaluated under alkaline pH condition similar to that found in repository environments. Different amounts of surfactant, equivalent to the 50, 100, and 200% cation-exchange capacity of the bentonite, were used to produce the HDTMA-SMB for iodide sorption. The sorption reaction of the SMB with iodide reached equilibrium rapidly within 10 min regardless of temperature and radiation conditions. The rate of iodide sorption increased as the amount of the added surfactant was increased and nonlinear sorption behavior was exhibited. However, high temperature and γ-irradiation ((60)Co) resulted in significantly (∼2-10 times) lower iodide Kd values for the SMB. The results of FTIR, NMR, and XANES spectroscopy analysis suggested that the decrease in iodide sorption may be caused by weakened physical electrostatic force between the HDTMA and iodide, and by the surfactant becoming detached from the SMB during the heating and irradiation processes.

  15. Effects of Radiation and Temperature on Iodide Sorption by Surfactant-Modified Bentonite

    SciTech Connect

    Choung, Sungwook; Kim, Min Kyung; Yang, Jungseok; Kim, Min-Gyu; Um, Wooyong

    2014-08-04

    Bentonite, which is used as an engineered barrier in geological repositories, is ineffective for sorbing anionic radionuclides because of its negatively charged surface. This study modified raw bentonite using a cationic surfactant (i.e., hexadecyltrimethylammonium [HDTMA]-Br) to improve its sorption capability for radioactive iodide. The effects of temperature and radiation on the iodide sorption of surfactant-modified bentonite (SMB) were evaluated under alkaline pH condition similar to that found in repository environments. Different amounts of surfactant, equivalent to the 50, 100, and 200% cation-exchange capacity of the bentonite, were used to produce the HDTMA-SMB for iodide sorption. The sorption reaction of the SMB with iodide reached equilibrium rapidly within 10 min regardless of temperature and radiation conditions. The rate of iodide sorption increased as the amount of the added surfactant was increased and nonlinear sorption behavior was exhibited. However, high temperature and γ-irradiation (60Co) resulted in significantly (~2–10 times) lower iodide Kd values for the SMB. The results of Fourier transform infrared spectroscopy analysis suggested that the decrease in iodide sorption may be caused by weakened physical electrostatic force between the HDTMA and iodide, and by the surfactant becoming detached from the SMB during the heating and irradiation processes.

  16. 21 CFR 520.763c - Dithiazanine iodide and piperazine citrate suspension.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Dithiazanine iodide and piperazine citrate... § 520.763c Dithiazanine iodide and piperazine citrate suspension. (a) Specifications. Each milliliter of... piperazine citrate). (b) Sponsor. See 000010 in § 510.600(c) of this chapter. (c) NAS/NRC status....

  17. 21 CFR 520.763c - Dithiazanine iodide and piperazine citrate suspension.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Dithiazanine iodide and piperazine citrate... § 520.763c Dithiazanine iodide and piperazine citrate suspension. (a) Specifications. Each milliliter of... piperazine citrate). (b) Sponsor. See 000010 in § 510.600(c) of this chapter. (c) NAS/NRC status....

  18. Efficient copper-catalyzed trifluoromethylation of aromatic and heteroaromatic iodides: the beneficial anchoring effect of borates.

    PubMed

    Gonda, Zsombor; Kovács, Szabolcs; Wéber, Csaba; Gáti, Tamás; Mészáros, Attila; Kotschy, András; Novák, Zoltán

    2014-08-15

    Efficient copper-catalyzed trifluoromethylation of aromatic iodides was achieved with TMSCF3 in the presence of trimethylborate. The Lewis acid was used to anchor the in situ generated trifluoromethyl anion and suppress its rapid decomposition. Broad applicability of the new trifluoromethylating reaction was demonstrated in the functionalization of different aromatic and heteroaromatic iodides. PMID:25068681

  19. Abiotic formation of methyl iodide on synthetic birnessite: a mechanistic study.

    PubMed

    Allard, Sébastien; Gallard, Hervé

    2013-10-01

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

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

    PubMed

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

    2016-09-28

    Mixed tin (Sn)-lead (Pb) perovskites with high Sn content exhibit low bandgaps suitable for fabricating the bottom cell of perovskite-based tandem solar cells. In this work, we report on the fabrication of efficient mixed Sn-Pb perovskite solar cells using precursors combining formamidinium tin iodide (FASnI3) and methylammonium lead iodide (MAPbI3). The best-performing cell fabricated using a (FASnI3)0.6(MAPbI3)0.4 absorber with an absorption edge of ∼1.2 eV achieved a power conversion efficiency (PCE) of 15.08 (15.00)% with an open-circuit voltage of 0.795 (0.799) V, a short-circuit current density of 26.86(26.82) mA/cm(2), and a fill factor of 70.6(70.0)% when measured under forward (reverse) voltage scan. The average PCE of 50 cells we have fabricated is 14.39 ± 0.33%, indicating good reproducibility. PMID:27622903

  1. 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.

  2. 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...

  3. 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

  4. 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)

  5. 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.

  6. 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

  7. Transport of Iodide Ion in Compacted Bentonite Containing Ag{sub 2}O - 12111

    SciTech Connect

    Yim, Sung Paal; Lee, Ji-Hyun; Choi, Heui-Joo; Choi, Jong-Won; Lee, Cheo Kyung

    2012-07-01

    Observations of the transport of iodide through compacted bentonite containing Ag{sub 2}O as additive and that without additive were made. Compacted bentonite samples with densities of 1.41 g/cm{sup 3} and 1.60 g/cm{sup 3} were used in the experiment. The amount of Ag{sub 2}O added to the compacted bentonite was in the range of 0.0064 ∼ 0.0468 wt/wt%. Two diffusion solutions were used: one in which iodide ion was dissolved in demineralized water (pure iodide solution), and one in which iodide ion was dissolved in 0.1 M NaCl solution (0.1 M NaCl-iodide solution). Experimental results confirmed that iodide ion was transported by the diffusion process in the compacted bentonite containing Ag{sub 2}O as well as in the compacted bentonite without Ag{sub 2}O. The time-lag of diffusion of iodide ion in the compacted bentonite containing Ag{sub 2}O is larger than that in the compacted bentonite without Ag{sub 2}O. The increase of the time-lag of diffusion was observed in pure iodide ion solution as well as in 0.1 M NaCl-iodide solution. The apparent diffusion coefficient of iodide ion in the compacted bentonite containing Ag{sub 2}O was smaller than in the compacted bentonite without Ag{sub 2}O. The effective diffusion coefficient decreased as the amount of Ag{sub 2}O in the compacted bentonite increased. (authors)

  8. 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 ...

  9. Synthesis and crystal structure of bis(1-{[(quinolin-8-yl)imino]methyl}pyrene-κ2 N,N′)silver(I) tri­fluoro­methane­sulfonate

    PubMed Central

    Pinto, Miguel; Chakraborty, Indranil; Mascharak, Pradip

    2016-01-01

    The title compound, [Ag(qPyr)2]CF3SO3 where qPyr = 1-(quinoline-2-yl­methyl­ene)amino­pyrene, C26H16N2, was synthesized from a reaction of silver tri­fluoro­methane­sulfonate and qPyr in di­chloro­methane–methanol mixed media. In this design, the qPyr ligand was chosen for its characteristic excitation and emission profiles, which could enable the tracking of the silver complex within biological targets. The AgI atom resides in a distorted tetra­hedral N4 coordination sphere. Analysis of the packing pattern revealed significant intra- and inter­molecular π–π stacking inter­actions between the [Ag(qPyr)2]+ cations. In addition, a weak C—H⋯O hydrogen bond consolidates the packing between cations and anions. PMID:27746949

  10. 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.

  11. 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...

  12. 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.

  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. 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

  15. VLSI readout for imaging with polycrystalline mercuric iodide detectors

    NASA Astrophysics Data System (ADS)

    Turchetta, Renato; Dulinski, Wojtek; Husson, D.; Klein, N.; Riester, J. L.; Schieber, Michael M.; Zuck, A.; Braiman, M.; Melekhov, L.; Nissenbaum, J.; Sanguinetti, S.

    1998-11-01

    Recently polycrystalline mercuric iodide have become available, for room temperature radiation detectors over large areas at low cost. Though the quality of this material is still under improvement, ceramic detectors have been already been successfully tested with dedicated low-noise, low-power mixed signal VLSI electronics which can be used for compact, imaging solutions. The detectors used are of different kinds: microstrips and pixels; of different sizes, up to about 1 square inch; and of different thickness, up to 600 microns. The properties of this first-generation detectors are quite uniform from one detector to another. Also for each single detector the response is quite uniform and no charge loss in the inter-electrode space have been detected. Because of the low cost and of the polycrystallinity, detectors can be potentially fabricated in any size and shape, using standard ceramic technology equipment, which is an attractive feature where low cost and large area applications are needed.

  16. 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.

  17. 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.

  18. Ultrafast Extreme Ultraviolet Absorption Spectroscopy of Methylammonium Lead Iodide Perovskite

    NASA Astrophysics Data System (ADS)

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

    2016-06-01

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

  19. 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.

  20. 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.

  1. Photodissociation of alkyl iodides in helium nanodroplets. III. Recombination

    SciTech Connect

    Braun, Andreas; Drabbels, Marcel

    2007-09-21

    The recombination of fragments resulting from the photodissociation of (fluorinated) alkyl iodides in helium nanodroplets at a wavelength of 266 nm has been investigated by means of ion imaging techniques. It is found that in the case of CH{sub 3}I an appreciable fraction of the fragments recombine in the aftermath of the photolysis. The proposed mechanism involves a complete translational relaxation of both photofragments inside the nanodroplets followed by geminate recombination of the fragments. In contrast with CH{sub 3}I, no recombination is observed for CF{sub 3}I. This is attributed to the larger masses and the different initial kinetic energies of the fragments produced by the photolysis of CF{sub 3}I, which strongly diminishes the fragment thermalization efficiency.

  2. 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

  3. 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.

  4. 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.

  5. 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.

  6. 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

  7. A passive ozone sampler based on a reaction with iodide.

    PubMed

    Yanagisawa, Y

    1994-02-01

    A new passive sampler for ozone and its simple analytical system have been developed. Because it is small and sensitive, the sampler can be used for determining personal exposures to ozone and oxidants and for multilocation measurements. The sampler consists of an electrode, a spacer, and several layers of membrane filters and Teflon meshes. The electrode is a carbon paper disk coated with nylon-6 polymer and potassium iodide. The membrane filters are used to remove interferences. A sampling rate of ozone is controlled by the spacer and Teflon meshes. Iodine is liberated by an oxidation reaction of potassium iodide with ozone. The iodine is stabilized by forming a charge transfer complex with nylon-6 and is accumulated in the nylon-6 layer. The amount of iodine, which is proportional to the level of ozone exposure, is quantified by constant current coulometry. The discharge time of a galvanic battery is measured using the electrode as a positive electrode and a zinc plate as a counter electrode. A time-weighted average concentration of ozone is derived from the discharge time after exposing the electrode to ozone. The effects of various environmental conditions on the sampler's performance were investigated. The results indicated that the sampler showed a linear response to ozone exposure up to 1,450 parts per billion for every hour of use (ppb.hour). The minimum detectable exposure was about 400 ppb.hour. The effects of surface wind velocity, temperature, and humidity were small. However, a relative humidity below 20% resulted in an underestimation of the ozone concentration. Because the electrode requires no pretreatment and the analytical method is very simple, this method is suitable for large-scale studies of personal exposures to ozone and oxidants using multilocation measurements.

  8. Electronic properties of the silver-silver chloride cluster interface.

    PubMed

    Glaus, Stephan; Calzaferri, Gion; Hoffmann, Roald

    2002-04-15

    The objective of this study was to gain insight into the electronic structure of silver-silver chloride cluster composites and especially into the metal-semiconductor interface. For this purpose a theoretical study of (AgCl)(n) (n=4, 32, 108, 192, and 256), of Ag(m) (m=1-9, 30, 115, 276, and 409), and of the cluster composites Ag(115)-(AgCl)(192) and Ag(409)-(AgCl)(192) has been carried out. Density of levels (DOL), local density of levels (l-DOL), and projection of surface states, as well as projection of properties of individual atoms or groups of atoms obtained in molecular orbital calculations, are shown to be powerful tools for gaining deep insight into the properties of these large systems. The Ag(115)-(AgCl)(192) aggregate, consisting of a cubic Ag(115) cluster without corner atoms on top of a cubic (AgCl)(192) cluster, was found to be remarkably stable with a cluster-to-cluster distance of about 280 pm, and a geometry in which the number of bonding interactions between the silver atoms of Ag(115) and the chloride ions of (AgCl)(192) is at its maximum. A sharp jump in charge distribution occurs at the Ag(115)-(AgCl)(192) composite interface. The first AgCl slab picks up negative charge from the two adjacent silver slabs, so that in total the silver cluster is positively charged. In addition, the core of the silver cluster is positively charged with respect to its outermost layer. The main reason for the charge transfer from the silver cluster to the silver chloride is the newly formed MIGS (metal induced gap states) in the energy-gap range of the silver chloride and the MIdS (metal induced d states) in the d-orbital region. Their wave functions mix with orbitals of the silver cluster and with both the orbitals of the silver and the chloride ions of the silver chloride. The MIGS and the MIdS are of a quite localized nature. In them, nearest neighbor interactions dominate, with the exception of close-lying silver chloride surface states-which mix in to a large

  9. Testing iodized activated carbon filters with non-radioactive methyl iodide. Final report

    SciTech Connect

    Deitz, V.R.; Romans, J.B.

    1980-05-30

    Iodized carbons, impregnated with KIx(KI + xI2), were evaluated for trapping methyl iodide-127. In this method the complete effluent of the carbon is sampled and analyzed continuously. In contrast, the RDT-M16 test procedure counts the carbon and the back-up beds for the accumulated 131 species and no information is obtained for the interaction of the large amount of carrier methyl iodide-127 with the iodized charcoal. The test apparatus to measure the penetration of methyl iodide-127 is described and the calibration procedures are detailed. Results are given for the penetration of methyl iodide-127 through new activated carbons, carbons in service, and exhausted carbons withdrawn from service. The reduction in trapping efficiency with service is accompanied by the development of a maximum in the concentration of methyl iodide-127 during the air purge after the dose period. This behavior has escaped notice with methyl iodide-131 due to the way that test is made. The chromatographic holdup of methyl iodide-127 by carbons in service, together with the subsequent slow desorption step, could result in a dilution of the penetration iodine to acceptable levels under some conditions encountered in plant filter operations.

  10. 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.

  11. Synthesis, characterization and antimicrobial activity of water-soluble silver(i) complexes of metronidazole drug and selected counter-ions.

    PubMed

    Kalinowska-Lis, Urszula; Felczak, Aleksandra; Chęcińska, Lilianna; Zawadzka, Katarzyna; Patyna, Emilia; Lisowska, Katarzyna; Ochocki, Justyn

    2015-05-01

    A series of water-soluble silver(i) complexes of the type [Ag(MTZ)2X] [MTZ = 1-(2-hydroxyethyl)-2-methyl-5-nitro-1H-imidazole (metronidazole drug); X = NO3(-), ClO4(-), CF3COO(-), BF4(-) and CH3SO3(-)] was synthesised by the reactions of various Ag(i) salts with metronidazole (MTZ). All the complexes were characterized by ESI-MS spectrometry, solution NMR ((1)H and (13)C) and IR spectroscopy, and elemental analysis. Further evidence for the formation and molecular structure of all the complexes was provided by X-ray single-crystal crystallography. The different counter ions affect the crystal packing of the complexes and thus have an impact on the final geometries. The antimicrobial activities of the complexes against two Gram-positive strains: Staphylococcus aureus ATCC 6538, Staphylococcus epidermidis ATCC 12228, three Gram-negative strains: Pseudomonas aeruginosa ATCC 15442, Escherichia coli ATCC 25922, Proteus hauseri ATCC 13315 and yeast Candida albicans ATCC 10231 were evaluated and compared with antibacterial and antifungal properties of appropriate silver salts, metronidazole and silver sulfadiazine drugs. The newly synthesized compounds exhibited significant antibacterial activity against Gram-positive bacteria, better than the referenced silver sulfadiazine. The best active silver(i)-metronidazole complex contains a methanesulphonate counter-ion. Moreover, the complex inhibited the growth of yeast Candida albicans at a concentration 3-fold lower than that required for silver sulfadiazine. In addition, the complexes containing a tetrafluoroborate and a perchlorate as counter-ions were characterized as effective antibacterial agents against the tested Gram-negative bacteria.

  12. Silver stain for electron microscopy

    NASA Technical Reports Server (NTRS)

    Corbett, R. L.

    1972-01-01

    Ammoniacal silver stain used for light microscopy was adapted advantageously for use with very thin biological sections required for electron microscopy. Silver stain can be performed in short time, has more contrast, and is especially useful for low power electron microscopy.

  13. 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.

  14. Silver against Pseudomonas aeruginosa biofilms.

    PubMed

    Bjarnsholt, Thomas; Kirketerp-Møller, Klaus; Kristiansen, Søren; Phipps, Richard; Nielsen, Anne Kirstine; Jensen, Peter Østrup; Høiby, Niels; Givskov, Michael

    2007-08-01

    Silver has been recognized for its antimicrobial properties for centuries. Most studies on the antibacterial efficacy of silver, with particular emphasis on wound healing, have been performed on planktonic bacteria. Our recent studies, however, strongly suggest that colonization of wounds involves bacteria in both the planktonic and biofilm modes of growth. The action of silver on mature in vitro biofilms of Pseudomonas aeruginosa, a primary pathogen of chronic infected wounds, was investigated. The results show that silver is very effective against mature biofilms of P. aeruginosa, but that the silver concentration is important. A concentration of 5-10 mug/mL silver sulfadiazine eradicated the biofilm whereas a lower concentration (1 mug/mL) had no effect. The bactericidal concentration of silver required to eradicate the bacterial biofilm was 10-100 times higher than that used to eradicate planktonic bacteria. These observations strongly indicate that the concentration of silver in currently available wound dressings is much too low for treatment of chronic biofilm wounds. It is suggested that clinicians and manufacturers of the said wound dressings consider whether they are treating wounds primarily colonized either by biofilm-forming or planktonic bacteria.

  15. Problem of the sorption trapping of radioactive iodine in the form of methyl iodide

    SciTech Connect

    Nakhutin, I.E.; Smirnova, N.M.; Poluektov, P.P.; Tret'yak, S.A.

    1987-12-01

    The purpose of this work is to study possibilities for raising the efficiency of the removal of methyl iodide from gases. The authors investigated the sorption trapping of methyl iodide in a chromatographic column with activated carbon of the SKT type with different bulk density without impregnants and after impregnation, and in addition the moisture content of the air was varied in different experiments. We studied the effect of the gas velocity in the column on the purification process. A scheme is proposed for processing the experimental data, and recommendations are given for selecting the carbon for removing methyl iodide from gases.

  16. Multiple-overtone resonance Raman scattering and fluorescence from I{sub 2} species adsorbed on silver surfaces

    SciTech Connect

    Sibbald, M.S.; Chumanov, G.; Small, G.; Cotton, T.M.

    1998-07-01

    A detailed excitation profile of a Raman progression consisting of up to six overtones and a fundamental band at 123 cm{sup {minus}1} observed from iodide adsorbed on an electrochemically roughened silver surface at 20 K is analyzed. The excitation profile was constructed from 77 spectra obtained by tuning the laser wavelength in {approximately}0.25 nm steps through the spectral range 409 nm{endash}433 nm. The shift between resonances in the excitation profile, corresponding to the spacing between vibronic levels in the excited state, is also equal to 123 cm{sup {minus}1} indicating that the ground state and excited state potential energy surfaces have the same shape. Only two distinct resonances spaced three vibrational quanta apart were evident in the profile for each band in the progression. Curve fitting of the Raman band shapes indicates that each overtone is composed of one sharp and one broad band, whereas the fundamental contains only one sharp component. The measured width of the fundamental was less than 2.5 cm{sup {minus}1} FWHM, limited by the instrument function. It is proposed that the sharp Raman bands represent a normal vibrational mode of a surface-adsorbed I{sub 2}-like species with the width determined by the intrinsic vibrational dephasing in the ground state. On the other hand, the broad Raman bands reflect vibronic coupling between different I{sub 2}-like species adsorbed on the same Ag cluster. The broad bandwidths result from both dephasing associated with the vibronic coupling and the intrinsic vibrational dephasing. Other weak emission bands are attributed to resonance fluorescence corresponding to direct transitions from higher vibronic levels of the excited state to the ground state. An emission at 429.9 nm is assigned to exciton recombination in small silver iodide clusters which are formed after spontaneous oxidation of the iodide-modified silver surface. {copyright} {ital 1998 American Institute of Physics.}

  17. 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…

  18. 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.

  19. 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.

  20. 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

  1. 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.

  2. 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.

  3. Moisture proof columnar Cesium Iodide (CsI) layers for gas avalanche microdetectors

    SciTech Connect

    Park, I.J.; Cho, H.S.; Hong, W.S.; Perez-Mendez, V.; Kadyk, J.

    1999-05-05

    Cesium iodide columnar layers having a diameter of 3 {micro}m, and wall spacing of {approx} 1 {micro}m act as secondary electron emitters and can be used for detection of radiation: charged particles, X-rays and gamma rays. With a large enough electric field across the columnar layers, {approx} 400 {micro}m in thickness, gas avalanche gain is evident when placed in a suitable gas, such as P10 or argon-ethane mixtures. The cesium iodide columns are damaged by ambient moisture. This damage can be prevented by evaporating protective layers of insoluble, low boiling point inorganic materials, such as mercuric iodide. Columnar layers with 20 nm coatings of mercuric iodide yield more than 30,000 electrons on average when traversed by electrons from a {sup 90}Sr beta source.

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

    PubMed

    Celo, Valbona; Scott, Susannah L

    2005-04-01

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

  5. 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.

  6. 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.

  7. 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.

  8. 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

  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.

  10. Syntheses, structures and properties of Mn(II), Zn(II) and Ag(I) coordination polymers with 2-(1,2,4-triazol-1-yl)acetate

    NASA Astrophysics Data System (ADS)

    Qian, Xin; Sun, Peng-Peng; Ding, Jian-Gang; Li, Bao-Long; Li, Han-Yan

    2013-01-01

    The self-assembly reaction of 2-(1,2,4-triazol-1-yl)acetic acid (Htza) with Mn(II), Zn(II) and Ag(I) salts gave three coordination polymers [Mn(tza)2]n (1), [Zn(tza)2]n (2) and [Ag3(tza)2(ClO4)]n (3). 1 has a (3,6)-connected CdCl2-type two-dimensional network. 2 is a neutral two-dimensional (4,4) network. However 3 shows the complicated two-dimensional undulated network. 2 and 3 exhibit blue luminescent emissions maxima at 420 and 437 nm, respectively in the solid state at room temperature. The thermal stability of 1, 2 and 3 were observed. The diffuse reflectance UV-vis spectroscopy of 1, 2 and 3 were measured.

  11. Rainfall Enhancement by Dynamic Cloud Modification: Massive silver iodide seeding causes rainfall increases from single clouds over southern Florida.

    PubMed

    Woodley, W L

    1970-10-01

    In summary, the following points are made: 1) There are essentially two approaches to seeding for rain inducement, static and dynamic. 2) The dynamic approach is effective in inducing growth and increasing precipitation from individually seeded convective clouds under specifiable conditions. 3) The static approach to seeding for precipitation increases is apparently not relevant to the summer cumuli of Florida and Missouri. 4) Regional seeding climatologies, including studies of natural freezing processes in convective clouds, should be completed before commencement of a seeding operation. 5) The results of a seeding operation are frequently better understood by stratification of the data, especially with respect to weather conditions. Precipitation increases from seeding are usually found under fair weather regimes with isolated showers, whereas decreases are often noted under naturally rainy conditions.

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

    PubMed

    Xianyu, Yunlei; Chen, Yiping; Jiang, Xingyu

    2015-11-01

    This report outlines an enzymatic cascade reaction for signal transduction and amplification for plasmonic immunoassays by using horseradish peroxidase (HRP)-mediated aggregation of gold nanoparticles (AuNPs). HRP-catalyzed oxidation of iodide and iodide-catalyzed oxidation of cysteine is employed to modulate the plasmonic signals of AuNPs. It agrees well with the current immunoassay platforms and allows naked-eye readout with enhanced sensitivity, which holds great promise for applications in resource-constrained settings. PMID:26460152

  13. Permeation of iodide from iodine-enriched yeast through porcine intestine.

    PubMed

    Ryszka, Florian; Dolińska, Barbara; Zieliński, Michał; Chyra, Dagmara; Dobrzański, Zbigniew

    2013-01-01

    Iodine deficiency is a common phenomenon, threatening the whole global human population. Recommended daily intake of iodine is 150 μg for adults and 250 μg for pregnant and breastfeeding women. About 50% of human population can be at risk of moderate iodine deficiency. Due to this fact, increased iodine supplementation is recommended, through intake of iodized mineral water and salt iodization. The aim of this study was to investigate permeation and absorption of iodide from iodine bioplex (experimental group) in comparison with potassium iodide (controls). Permeation and absorption processes were investigated in vitro using a porcine intestine. The experimental model was based on a standard Franz diffusion cell (FD-Cell). The iodine bioplex was produced using Saccharomyces cerevisiae yeast and whey powder: iodine content - 388 μg/g, total protein - 28.5%, total fat - 0.9%., glutamic acid - 41.2%, asparaginic acid - 29.4%, lysine - 24.8%; purchased from: F.Z.N.P. Biochefa, Sosnowiec, Poland. Potassium iodide was used as controls, at 388 μg iodine concentration, which was the same as in iodine-enriched yeast bioplex. A statistically significant increase in iodide permeation was observed for iodine-enriched yeast bioplex in comparison with controls - potassium iodide. After 5h the total amount of permeated iodide from iodine-enriched yeast bioplex was 85%, which is ~ 2-fold higher than controls - 37%. Iodide absorption was by contrast statistically significantly higher in controls - 7.3%, in comparison with 4.5% in experimental group with iodine-enriched yeast bioplex. Presented results show that iodide permeation process dominates over absorption in case of iodine-enriched yeast bioplex.

  14. Determination of iodide in ground water and soil by ion chromatography.

    PubMed

    Tucker, H L; Flack, R W

    1998-04-24

    Comprehensive elemental analysis of samples from the Bear Creek Valley near the Oak Ridge Y-12 Plant, and its floodplain have been performed in order to allow an unclassified assessment of possible elemental contamination within this area. A rapid ion Chromatographic method, with isocratic separation and micromembrane suppression is discussed within this paper for the analysis of iodide in soils, and floodplain ground waters. This developmental method will be used for future routine iodide analysis.

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

    PubMed

    Xianyu, Yunlei; Chen, Yiping; Jiang, Xingyu

    2015-11-01

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

  16. 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.

  17. 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

  18. Physical mechanisms for anisotropic plasma etching of cesium iodide

    SciTech Connect

    Yang Xiaoji; Hopwood, Jeffrey A.

    2004-11-01

    The physical mechanisms for the interaction between a reactive plasma and a cesium iodide surface are investigated. Under conditions of ion bombardment and elevated substrate temperature, CsI is found to sputter etch slowly (15 nm/min). If atomic fluorine, fluorocarbon radicals, of SF{sub x} radicals are present in the discharge, however, CsI is reactively etched at substantially higher rates (up to 200 nm/min). The roles of plasma radicals and energetic ion bombardment are investigated by first exposing the surface to plasma radicals and then bombarding the surface with argon ions. The optical emission from Cs and I atoms is found to correlate with the etch rate of CsI and is used as an in situ monitor of radical-enhanced etching. Small surface exposures to CF{sub x}, SF{sub x}, and F radicals are shown to enhance the etch rate of CsI. If the exposure of the CsI surface is increased, however, these same radical species act as etch inhibitors. A simple model for reactive etching of CsI is proposed, and this model is shown to compare reasonably well with experimental etch rates.

  19. 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

  20. 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.

  1. 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.

  2. 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.

  3. Interfacial Charge Transfer Anisotropy in Polycrystalline Lead Iodide Perovskite Films.

    PubMed

    Yin, Jun; Cortecchia, Daniele; Krishna, Anurag; Chen, Shi; Mathews, Nripan; Grimsdale, Andrew C; Soci, Cesare

    2015-04-16

    Solar cells based on organic-inorganic lead iodide perovskite (CH3NH3PbI3) exhibit remarkably high power conversion efficiency (PCE). One of the key issues in solution-processed films is that often the polycrystalline domain orientation is not well-defined, which makes it difficult to predict energy alignment and charge transfer efficiency. Here we combine ab initio calculations and photoelectron spectroscopy to unravel the electronic structure and charge redistribution at the interface between different surfaces of CH3NH3PbI3 and typical organic hole acceptor Spiro-OMeTAD and electron acceptor PCBM. We find that both hole and electron interfacial transfer depend strongly on the CH3NH3PbI3 surface orientation: while the (001) and (110) surfaces tend to favor hole injection to Spiro-OMeTAD, the (100) surface facilitates electron transfer to PCBM due to surface delocalized charges and hole/electron accumulation at the CH3NH3PbI3/organic interfaces. Molecular dynamic simulations indicate that this is due to strong orbital interactions under thermal fluctuations at room temperature, suggesting the possibility to further improve charge separation and extraction in perovskite-based solar cells by controlling perovskite film crystallization and surface orientation.

  4. 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.

  5. A simple sperm nuclear vacuole assay with propidium iodide.

    PubMed

    Zhu, W-J; Li, J

    2015-09-01

    Our aim was to develop a new simple sperm nuclear vacuole assay (SNVA) with propidium iodide (PI) to determine the status of nuclear vacuole (NV) of individual spermatozoa. After PI staining, sperm nuclei were classified into the 14 categories according to both nuclear morphology and the status of NV. The incidence was 57.8% (range 28-84%) in fertile controls (n = 40), and 85.1% (range 67-99%) in men with varicocele (n = 40). In the fertile group, normal nuclear-shaped spermatozoa without NV or with one small NV located in the ante-nuclear region were significantly more in comparison with the varicocele group. In the varicocele group, abnormal nuclear-shaped spermatozoa with one large NV and with multiple NVs located in the ante-nuclear region were most frequent findings. Besides, spermatozoa with NVs in both ante- and post-nuclear regions in the varicocele group were significantly more than those in the fertile group. In both fertile and varicocele groups, normal or abnormal nuclear-shaped spermatozoa with one or more vacuoles only located in the post-nuclear region occurred sparingly. The SNVA provides a useful additional approach to identify the status of NV in human spermatozoa for diagnostic purposes. A good sperm sample would have more spermatozoa without NV or with one small NV located in the ante-nuclear region.

  6. 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.

  7. The effect of hydrogen coadsorption on the thermal chemistry of methyl iodide on Ni(100) surfaces

    SciTech Connect

    Tjandra, S.; Zaera, F. )

    1993-12-01

    A detailed investigation of the surface chemistry of methyl iodide with preadsorbed hydrogen on Ni(100) is reported here. TPD data indicate that, in general, the presence of hydrogen on the surface induces a yield increase in methane formation and a reduction of the extent of which methyl species decompose as compared with the case where the methyl iodide is adsorbed by itself on a clean surface. Furthermore, two very different methane desorption regimes are observed at 150 and 220 K. By using both isotopically labelled methyl iodide and deuterium (D[sub 2] + CH[sub 3]I and H[sub 2] + CD[sub 3]I) it was determined that while the high-temperature methane is formed via the reductive elimination of surface methyl species produced by decomposition of methyl iodide with coadsorbed hydrogen atoms, the lower temperature methane TPD peak may be the result of a direct attack of the surface hydrogen on adsorbed methyl iodide molecules in a concerted fashion instead. The TPD data also indicate that neither methylene nor methylidyne intermediates form during the decomposition of methyl iodide on nickel below 200 K, and experiments with CH[sub 2]I[sub 2] clearly show that methylene species can be easily hydrogenated to methane in the presence of D[sub 2] coadsorption at quite low temperatures. Finally, no H-D exchange between methyl species and coadsorbed hydrogen (H[sub 2]) was observed. 44 refs., 20 figs.

  8. 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.

  9. 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.

  10. 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.

  11. Metallogels derived from silver coordination polymers of C3-symmetric tris(pyridylamide) tripodal ligands: synthesis of Ag nanoparticles and catalysis.

    PubMed

    Paul, Mithun; Sarkar, Koushik; Dastidar, Parthasarathi

    2015-01-01

    By applying a recently developed crystal engineering rationale, four C3 symmetric tris(pyridylamide) ligands namely 1,3,5-tris(nicotinamidomethyl)-2,4,6-triethylbenzene, 1,3,5-tris(isonicotinamidomethyl)-2,4,6-triethylbenzene, 1,3,5-tris(nicotinamidomethyl)-2,4,6-trimethylbenzene, and 1,3,5-tris(isonicotinamidomethyl)-2,4,6-trimethylbenzene, which contain potential hydrogen-bonding sites, were designed and synthesized for generating Ag(I) coordination polymers and coordination-polymer-based gels. The coordination polymers thus obtained were characterized by single-crystal X-ray diffraction. The silver metallogels were characterized by transmission electron microscopy (TEM) and dynamic rheology. Upon exposure to visible light, these silver metallogels produced silver nanoparticles (AgNPs), which were characterized by TEM, powder X-ray diffraction, energy dispersive X-ray and X-ray photoelectron spectroscopy. These NPs were found to be effectively catalyzed the reduction of 4-nitrophenolate to 4-aminophenolate without the use of any exogenous reducing agent.

  12. 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.

  13. 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.

  14. 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

  15. Antimicrobial effects of silver zeolite, silver zirconium phosphate silicate and silver zirconium phosphate against oral microorganisms

    PubMed Central

    Saengmee-anupharb, Sirikamon; Srikhirin, Toemsak; Thaweboon, Boonyanit; Thaweboon, Sroisiri; Amornsakchai, Taweechai; Dechkunakorn, Surachai; Suddhasthira, Theeralaksna; Kamaguchi, Arihide

    2013-01-01

    Objective To evaluate the antimicrobial activities of silver inorganic materials, including silver zeolite (AgZ), silver zirconium phosphate silicate (AgZrPSi) and silver zirconium phosphate (AgZrP), against oral microorganisms. In line with this objective, the morphology and structure of each type of silver based powders were also investigated. Methods The antimicrobial activities of AgZ, AgZrPSi and AgZrP were tested against Streptococcus mutans, Lactobacillus casei, Candida albicans and Staphylococcus aureus using disk diffusion assay as a screening test. The minimum inhibitory concentration (MIC) and minimum lethal concentration (MLC) were determined using the modified membrane method. Scanning electron microscope and X-ray diffraction were used to investigate the morphology and structure of these silver materials. Results All forms of silver inorganic materials could inhibit the growth of all test microorganisms. The MIC of AgZ, AgZrPSi and AgZrP was 10.0 g/L whereas MLC ranged between 10.0–60.0 g/L. In terms of morphology and structure, AgZrPSi and AgZrP had smaller sized particles (1.5–3.0 µm) and more uniformly shaped than AgZ. Conclusions Silver inorganic materials in the form of AgZ, AgZrPSi and AgZrP had antimicrobial effects against all test oral microorganisms and those activities may be influenced by the crystal structure of carriers. These results suggest that these silver materials may be useful metals applied to oral hygiene products to provide antimicrobial activity against oral infection. PMID:23570016

  16. 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.

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

    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.

  18. 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.

  19. Vapor growth of mercuric iodide tetragonal prismatic crystals

    NASA Astrophysics Data System (ADS)

    Ariesanti, Elsa

    The effect of polyethylene addition on the growth of mercuric iodide (HgI2) tetragonal prismatic crystals is examined. Three types of polyethylene powder are utilized: low molecular weight (Mw ˜ 4 x 103), ultra high molecular weight (Mw ˜ 3-6 x 1066), and spectrophotometric grade polyethylenes. Among these types of polyethylene, the low molecular weight polyethylene produces the most significant change in HgI2 morphology, with {110} being the most prominent crystal faces. Thermal desorption - gas chromatography/ mass spectroscopy (TD-GC/MS) studies show that thermal desorption of the low molecular weight polyethylene at 100°C and 150°C produce isomers of alkynes, odd nalkanes, and methyl (even-n) alkyl ketones. HgI2 growth runs with n-alkanes, with either neicosane, n-tetracosane, or n-hexatriacontane, cannot replicate the crystal shapes produced during growth with the low molecular weight polyethylene, whereas HgI2 growth runs with ketones, with either 3-hexadecanone or 14-heptacosanone, produce HgI2 tetragonal prismatic crystals, similar to the crystals grown with the low molecular weight polyethylene. C-O double bond contained in any ketone is a polar bond and this polar bond may be attracted to the mercury atoms on the top-most layer of the {110} faces through dipoledipole interaction. As a result, the growth of the {110} faces is impeded, with the crystals elongated in the [001] direction and bounded by the {001} faces along with large, prismatic {110} faces.

  20. 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.

  1. Specific binding modes of Cu(I) and Ag(I) with neurotoxic domain of the human prion protein.

    PubMed

    Valensin, Daniela; Padula, Emilia Maria; Hecel, Aleksandra; Luczkowski, Marek; Kozlowski, Henryk

    2016-02-01

    Prion diseases are neurodegenerative disorders associated with a conformational change of the normal cellular isoform of the prion protein (PrP(C)) to an abnormal scrapie isoform (PrP(Sc)). human prion protein (hPrP(C)) is able to bind up to six Cu(II) ions. Four of them are distributed in the octarepeat domain, containing four tandem-repetitions of the sequence PHGGGWGQ. Immediately outside the octarepeat domain, in so called PrP amyloidogenic region, two additional and independent Cu(II) binding sites, encompassing His96 and His111 residues, respectively, are present. Considering the potential involvement of PrP in cellular redox homeostasis, investigations on Cu(I)-PrP interaction might be also biologically relevant. Interestingly, the amyloidogenic fragment of PrP contains a -M(X)nM- motif, known to act as Cu(I) binding site in different proteins. In order to shed more light on this issue, copper(I) and silver(I) interactions with model peptides derived from that region were analyzed. The results of our studies reveal that both metal ions are anchored to two thioether sulfurs of Met109 and Met112, respectively. Subsequent metal interaction and coordination to His96 and His111 imidazoles are primarily found for Cu(I) at physiological pH. Metal binding was also investigated in the presence of negatively charged micelles formed by the anionic surfactant, sodium dodecyl sulfate (SDS). Our results strongly support that metal binding mode strongly depends on the protein backbone structure. In particular we show that α-helix structuring of the amyloid PrP domain influences both the metal coordination sphere and the binding affinity. PMID:26606290

  2. 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

  3. 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.

  4. Silver composite cathodes for alkaline secondary batteries

    NASA Astrophysics Data System (ADS)

    Ferrando, William A.

    1989-08-01

    This invention relates to electrochemical cells and more particularly to silver electrodes for electrochemical cells. Accordingly, an object of this invention is to provide a new, lighter weight silver electrode for secondary cells. Another object of this invention is to provide an electrode which requires less silver to operate. A further object of this invention is to provide a silver electrode which uses the silver more efficiently. Yet another object of the invention is to provide an easier, less expensive method of manufacturing silver electrodes for secondary cells.

  5. 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.

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

    PubMed

    Lin, Li; Wang, Haibo; Shi, Yali

    2013-03-01

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

  7. The sodium iodide symporter (NIS): regulation and approaches to targeting for cancer therapeutics.

    PubMed

    Kogai, Takahiko; Brent, Gregory A

    2012-09-01

    Expression of the sodium iodide symporter (NIS) is required for efficient iodide uptake in thyroid and lactating breast. Since most differentiated thyroid cancer expresses NIS, β-emitting radioactive iodide is routinely utilized to target remnant thyroid cancer and metastasis after total thyroidectomy. Stimulation of NIS expression by high levels of thyroid-stimulating hormone is necessary to achieve radioiodide uptake into thyroid cancer that is sufficient for therapy. The majority of breast cancer also expresses NIS, but at a low level insufficient for radioiodine therapy. Retinoic acid is a potent NIS inducer in some breast cancer cells. NIS is also modestly expressed in some non-thyroidal tissues, including salivary glands, lacrimal glands and stomach. Selective induction of iodide uptake is required to target tumors with radioiodide. Iodide uptake in mammalian cells is dependent on the level of NIS gene expression, but also successful translocation of NIS to the cell membrane and correct insertion. The regulatory mechanisms of NIS expression and membrane insertion are regulated by signal transduction pathways that differ by tissue. Differential regulation of NIS confers selective induction of functional NIS in thyroid cancer cells, as well as some breast cancer cells, leading to more efficient radioiodide therapy for thyroid cancer and a new strategy for breast cancer therapy. The potential for systemic radioiodide treatment of a range of other cancers, that do not express endogenous NIS, has been demonstrated in models with tumor-selective introduction of exogenous NIS.

  8. One-Step Deposition of Photovoltaic Layers Using Iodide Terminated PbS Quantum Dots.

    PubMed

    Kim, Sungwoo; Noh, Jaehong; Choi, Hyekyoung; Ha, Heonseok; Song, Jung Hoon; Shim, Hyung Cheoul; Jang, Jihoon; Beard, Matthew C; Jeong, Sohee

    2014-11-20

    We present a one-step layer deposition procedure employing ammonium iodide (NH4I) to achieve photovoltaic quality PbS quantum dot (QD) layers. Ammonium iodide is used to replace the long alkyl organic native ligands binding to the QD surface resulting in iodide terminated QDs that are stabilized in polar solvents such as N,N-dimethylformamide without particle aggregation. We extensively characterized the iodide terminated PbS QD via UV-vis absorption, transmission electron microscopy (TEM), thermogravimetric analysis (TGA), FT-IR transmission spectroscopy, and X-ray photoelectron spectroscopy (XPS). Finally, we fabricated PbS QD photovoltaic cells that employ the iodide terminated PbS QDs. The resulting QD-PV devices achieved a best power conversion efficiency of 2.36% under ambient conditions that is limited by the layer thickness. The PV characteristics compare favorably to similar devices that were prepared using the standard layer-by-layer ethandithiol (EDT) treatment that had a similar layer thickness.

  9. Catalytic spectrophotometric determination of iodide in pharmaceutical preparations and edible salt.

    PubMed

    El-Ries, M A; Khaled, Elmorsy; Zidane, F I; Ibrahim, S A; Abd-Elmonem, M S

    2012-02-01

    The catalytic effect of iodide on the oxidation of four dyes: viz. variamine blue (VB), methylene blue (MB), rhodamine B (RB), and malachite green (MG) with different oxidizing agents was investigated for the kinetic spectrophotometric determination of iodide. The above catalyzed reactions were monitored spectrophotometrically by following the change in dye absorbances at 544, 558, 660, or 617 nm for the VB, RB, MB, or MG catalyzed reactions, respectively. Under optimum conditions, iodide can be determined within the concentration levels 0.064-1.27 µg mL(-1) for VB method, 3.20-9.54 µg mL(-1) for RB method, 5.00-19.00 µg mL(-1) for the MB method, and 6.4-19.0 µg mL(-1) for the MG one, with detection limit reaching 0.004 µg mL(-1) iodide. The reported methods were highly sensitive, selective, and free from most interference. Applying the proposed procedures, trace amounts of iodide in pharmaceutical and edible salt samples were successfully determined without separation or pretreatment steps.

  10. 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.

  11. Energy Loss and Stopping Cross Section Factors for Alphas in Lead Iodide

    NASA Astrophysics Data System (ADS)

    Magness, B.

    2005-03-01

    Lead Iodide is a candidate for use as a room temperature gamma ray sensitive semiconductor similar to mercuric iodide. We report here on values for the energy loss factor and the stopping cross section factor in lead iodide thin films. Vapor diffused purified lead iodide was used to make thick film and thin film samples evaporated on amorphic glass substrates. Thin films were used to take advantage of the surface energy approximation. In addition, separate lead and iodide backscattering peaks from the films are well resolved. Film thickness ranged from 50nm to 1000nm as determined by optical interference methods. The high energy singly ionized helium beam was provided by the CSULA 4 MeV Van de Graff accelerator. Rutherford backscattering was detected at 170^o. Both the input and output energy losses were calculated from the FWHM of the corresponding peaks. The typical energy loss factor was found to be 20.2 eV/angstrom with a 3% uncertainty for a 2.4 MeV input beam. As expected, this value is about one third that of the pure elements.

  12. 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

  13. 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.

  14. 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

  15. 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

  16. 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.

  17. 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.

  18. 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

  19. Simultaneous detection of iodine and iodide on boron doped diamond electrodes.

    PubMed

    Fierro, Stéphane; Comninellis, Christos; Einaga, Yasuaki

    2013-01-15

    Individual and simultaneous electrochemical detection of iodide and iodine has been performed via cyclic voltammetry on boron doped diamond (BDD) electrodes in a 1M NaClO(4) (pH 8) solution, representative of typical environmental water conditions. It is feasible to compute accurate calibration curve for both compounds using cyclic voltammetry measurements by determining the peak current intensities as a function of the concentration. A lower detection limit of about 20 μM was obtained for iodide and 10 μM for iodine. Based on the comparison between the peak current intensities reported during the oxidation of KI, it is probable that iodide (I(-)) is first oxidized in a single step to yield iodine (I(2)). The latter is further oxidized to obtain IO(3)(-). This technique, however, did not allow for a reasonably accurate detection of iodate (IO(3)(-)) on a BDD electrode.

  20. 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

  1. A new route towards the synthesis of multi-tritiomethyl iodide

    SciTech Connect

    Saljoughian, M.; Morimoto, H.; Rapoport, H.

    1988-06-01

    A new procedure for the synthesis of multi-tritiated methyl iodide is reported. In this procedure trichloromethylphenyl sulfide was prepared and the trichloromethyl group was hydrogenolysed in the presence of 10% Pd/C and an organic base with deuterium gas to give the corresponding deuterated sulfide as the precursor. Upon heating a mixture of the latter with excess of benzyl iodide in a special apparatus benzylphenyl sulfide remained as a solid by-product and liberated deuteriated methyl iodide was directly reacted with several simple amines to be N-deuteriomethylated. This new synthetic method can be extended to the tritiomethyl labeling of a variety of organic compounds having a methyl group attached to a heteroatom such as N, O and S. 12 refs.

  2. 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

  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. 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…

  6. Synthesis, optical properties and ultrafast electronic relaxation of layered semiconductor nanoparticles: Lead iodide, bismuth iodide, bismuth sulfide

    NASA Astrophysics Data System (ADS)

    Sengupta, Archita

    The first direct observation of the electronic relaxation dynamics in PbI2, BiI3 and Bi2S3 nanoparticles using femtosecond transient spectroscopy has been reported. The nanoparticles were synthesized in polar and nonpolar solvents, polymer matrices and inverse micelles using colloidal chemistry methods and in thin films. The particle sizes were determined using TEM which provided direct evidence of photodegradation of nanoparticles. The ground state electronic absorption spectra of PbI 2 and BiI3 colloidal nanoparticles show well-resolved peaks in the near UV and visible region. Using a particle in an anisotropic box model the blue shift and increase in absorption of these peaks with simultaneous decrease in particle size have been explained. The UV-visible absorption spectra of Bi2S3 colloidal nanoparticles have very different features compared to those of PbI2 and BiI3 nanoparticles. Similarities and differences found among these nanoparticle systems, PbI 2, BiI3 and Bi2S3, in terms of optical properties and femtosecond electronic relaxation dynamics have been discussed. For PbI2, BiI3 and Bi2S3 with excitation at 390 nm and probing in the near infrared, the electronic relaxation dynamics were directly monitored and found to be sensitive to solvent and insensitive to particle size. For both PbI2 and BiI3 there appeared to be an oscillatory feature at early times with a period changing with solvent but not with particle size. However, for BiI3, the oscillation periods were slightly shorter and overall relaxation was somewhat faster than that in PbI2. The possibilities of the origin of this feature have been addressed. For Bi2S3 system, the early time dynamics did not show any resolvable oscillation. It could be due to the fact that the origin of oscillations in PbI2 and BiI3 nanoparticle system is connected to layered iodide structure and thus is not found in layered sulfide structure or the feature was not observed due to overall fast relaxation in Bi2S3

  7. Exploring the interaction between the human copper transporter, CTR1, c-terminal domain and a methionine motif in the presence of Cu(I) and Ag(I) ions, using EPR spectroscopy

    NASA Astrophysics Data System (ADS)

    Shenberger, Yulia; Yarmiayev, Valeria; Ruthstein, Sharon

    2013-10-01

    The essentiality and toxicity of copper in human, yeast, and bacteria cells requires precise mechanisms for acquisition, intimately linked to controlled distribution, which have yet to be fully understood. Herein, we utilise continuous wave and pulsed electron paramagnetic resonance (EPR) spectroscopy to explore one aspect in the controlled copper transportation mechanism. This was achieved by probing structural changes that occur in the c-terminal domain of the human copper transporter, CTR1, upon interacting with a methionine segment. The copper transporter CTR1 transports Cu(I) and Ag(I) ions to various intracellular pathways. Methionine motifs are methionine-rich metal binding segments found in many proteins involved in the transportation of copper ions to other cellular pathways. They are also found to bind Ag(I) with an affinity comparable to Cu(I). This study indicates that the methionine motif experiences conformational changes in the presence of the CTR1 c-terminal domain. These structural changes are dependent on the nature of the metal ion, Cu(I) vs. Ag(I). In addition, the data collected in this study emphasise how important the cysteine residue of the CTR1 c-terminal domain is to a correct conformational state of the target metal binding site.

  8. 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.

  9. 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.

  10. 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.

  11. Modeling of Turing Structures in the Chlorite-Iodide-Malonic Acid-Starch Reaction System

    NASA Astrophysics Data System (ADS)

    Lengyel, Istivan; Epstein, Irving R.

    1991-02-01

    Recent experiments on the chlorite-iodide-malonic acid-starch reaction in a gel reactor give the first evidence of the existence of the symmetry breaking, reaction-diffusion structures predicted by Turing in 1952. A five-variable model that describes the temporal behavior of the system is reduced to a two-variable model, and its spatial behavior is analyzed. Structures have been found with wavelengths that are in good agreement with those observed experimentally. The gel plays a key role by binding key iodine species, thereby creating the necessary difference in the effective diffusion coefficients of the activator and inhibitor species, iodide and chlorite ions, respectively.

  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. 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.

  14. Photoemission and optical constant measurements of a Cesium Iodide thin film photocathode

    NASA Astrophysics Data System (ADS)

    Triloki; Rai, R.; Gupta, Nikita; Jammal, Nabeel F. A.; Singh, B. K.

    2015-07-01

    The performance of cesium iodide as a reflective photocathode is presented. The absolute quantum efficiency of a 500 nm thick film of cesium iodide has been measured in the wavelength range 150 nm-200 nm. The optical absorbance has been analyzed in the wavelength range 190 nm-900 nm and the optical band gap energy has been calculated. The dispersion properties were determined from the refractive index using an envelope plot of the transmittance data. The morphological and elemental film composition have been investigated by atomic force microscopy and X-ray photo-electron spectroscopy techniques.

  15. 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

  16. AgI alloying in SnTe boosts the thermoelectric performance via simultaneous valence band convergence and carrier concentration optimization

    NASA Astrophysics Data System (ADS)

    Banik, Ananya; Biswas, Kanishka

    2016-10-01

    SnTe, a Pb-free analogue of PbTe, was earlier assumed to be a poor thermoelectric material due to excess p-type carrier concentration and large energy separation between light and heavy hole valence bands. Here, we report the enhancement of the thermoelectric performance of p-type SnTe by Ag and I co-doping. AgI (1-6 mol%) alloying in SnTe modulates its electronic structure by increasing the band gap of SnTe, which results in decrease in the energy separation between its light and heavy hole valence bands, thereby giving rise to valence band convergence. Additionally, iodine doping in the Te sublattice of SnTe decreases the excess p-type carrier concentration. Due to significant decrease in hole concentration and reduction of the energy separation between light and heavy hole valence bands, significant enhancement in Seebeck coefficient was achieved at the temperature range of 600-900 K for Sn1-xAgxTe1-xIx samples. A maximum thermoelectric figure of merit, zT, of ~1.05 was achieved at 860 K in high quality crystalline ingot of p-type Sn0.95Ag0.05Te0.95I0.05.

  17. 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.

  18. 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…

  19. 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

  20. Mineral resource of the month: silver

    USGS Publications Warehouse

    Brooks, William E.

    2007-01-01

    Silver has been used for thousands of years as ornaments and utensils, for trade and as the basis of many monetary systems. The metal has played an important part in world history. Silver from the mines at Laurion, Greece, for example, financed the Greek victory over the Persians in 480 B.C. Silver from Potosi, Bolivia, helped Spain become a world power in the 16th and 17th centuries. And silver from the gold-silver ores at the Comstock Lode in Virginia City, Nev., helped keep the Union solvent during the Civil War.

  1. Self-assembly of 1D mixed-metal tubular network with coordination bonds through the interconnection of organometallic metallamacrocycles by Ag(I) centers.

    PubMed

    Wang, Guo-Liang; Lin, Yue-Jian; Jin, Guo-Xin

    2011-05-21

    The combination of a ditopic ligand containing a functional "third site" as a bridge and organometallic half-sandwich iridium unit Cp*Ir as the corner leads to the formation of the tetranuclear metallamacrocycle 1, which is reacted with silver compound, resulting in the formation of mixed-metal infinitely tubular coordination network 2.

  2. 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.

  3. 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

  4. 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.

  5. Silver based batteries for high power applications

    NASA Astrophysics Data System (ADS)

    Karpinski, A. P.; Russell, S. J.; Serenyi, J. R.; Murphy, J. P.

    The present status of silver oxide-zinc technology and applications has been described by Karpinski et al. [A.P. Karpinski, B. Makovetski, S.J. Russell, J.R. Serenyi, D.C. Williams, Silver-Zinc: status of technology and applications, Journal of Power Sources, 80 (1999) 53-60], where the silver-zinc couple is still the preferred choice where high specific energy/energy density, coupled with high specific power/power density are important for high-rate, weight or size/configuration sensitive applications. Perhaps the silver oxide cathode can be considered one of the most versatile electrode materials. When coupled with other anodes and corresponding electrolyte management system, the silver electrode provides for a wide array of electrochemical systems that can be tailored to meet the most demanding, high power requirements. Besides zinc, the most notable include cadmium, iron, metal hydride, and hydrogen electrode for secondary systems, while primary systems include lithium and aluminum. Alloys including silver are also available, such as silver chloride, which when coupled with magnesium or aluminum are primarily used in many seawater applications. The selection and use of these couples is normally the result of a trade-off of many factors. These include performance, safety, risk, reliability, and cost. When high power is required, silver oxide-zinc, silver oxide-aluminum, and silver oxide-lithium are the most energetic. For moderate performance (i.e., lower power), silver oxide-zinc or silver-cadmium would be the system of choice. This paper summarizes the suitability of the silver-based couples, with an emphasis on the silver-zinc system, as primary or rechargeable power sources for high energy/power applications.

  6. Encapsulation of sodium radio-iodide in fullerene C₆₀.

    PubMed

    Valderrama, Alejandro; Guzman, José

    2014-03-01

    In this work we have studied the well-known "Buckminsterfullerene" C₆₀ containing different amounts, from one to four molecules, of sodium radio-iodide (Na(131)I), with density functional theory geometrical optimizations and molecular dynamics at 310 K and atmospheric pressure. We found that nanocapsules with the radioactive content Na¹³¹I@C₆₀, 2Na¹³¹I@C₆₀ and 3Na¹³¹I@C₆₀ are stable. Furthermore, the C₆₀ fullerene undergoes expansion when the number of sodium radio-iodide molecules inside increases. Utilizing the Mulliken charge distribution analysis it was shown that a small charge transfer occurs from iodine to fullerene's carbon atoms. This produces repulsion which increases bond lengths thus the structure is weakened while the binding energy per atom decreases. For the case in which the fullerene initially contains four sodium radio-iodide molecules the expansion is greater than that which the structure can withstand. So the fullerene breaks and releases its contents. This result leads us to conclude that the fullerene can encapsulate up to three molecules of sodium radio-iodide.

  7. Kinetics and Mechanism of Iodide Oxidation by Iron(III): A Clock Reaction Approach

    ERIC Educational Resources Information Center

    Bauer, Jurica; Tomisic, Vladislav; Vrkljan, Petar B. A.

    2008-01-01

    A simple method for studying the kinetics of a chemical reaction is described and the significance of reaction orders in deducing reaction mechanisms is demonstrated. In this student laboratory experiment, oxidation of iodide by iron(III) ions in an acidic medium is transformed into a clock reaction. By means of the initial rates method, it is…

  8. Determination of iodine in bread and fish using the iodide ion-selective electrode

    SciTech Connect

    Steiner, J.B.

    1985-01-01

    The purpose of this study was to assess the potential for use of the ion-selective electrode (ISE) as a method for measuring the iodine content in bread and fish. Ashing methods, sample preparation and electrode responses were evaluated. The iodine values obtained using the iodide electrode were compared to iodine values obtained by the arsenic-cerium method (As-Ce). Ashing methods were used in preparing bread and haddock for iodine analysis by the ISE. The values were compared to unashed samples measured by the ISE. Electrode response to iodide was examined by varying the sample pH, measuring electrode equilibrium times, and comparing direct measurement in ppm to iodide values obtained by the method of known addition. Oyster reference tissue with a known iodine concentration was used to determine rates of recovery. For the As-Ce procedure, an alkaline dry ash for two hour followed by colorimetric analysis at 320 nm was recommended. The study showed that the pre-treatment of bread and fish was necessary for ISE measurement. The iodine values obtained by the ISE in the analysis of oyster reference tissue, haddock and bread were not in agreement with their corresponding As-Ce values. Further work needs to be done to determine an ashing procedure that has minimal iodide loss an/or develop sample treatments that will improve the reliability and precision of iodine values obtained using the ion-selective electrode.

  9. Preparation and Luminescence Thermochromism of Tetranuclear Copper(I)-Pyridine-Iodide Clusters

    ERIC Educational Resources Information Center

    Parmeggiani, Fabio; Sacchetti, Alessandro

    2012-01-01

    A simple and straightforward synthesis of a tetranuclear copper(I)-pyridine-iodide cluster is described as a laboratory experiment for advanced inorganic chemistry undergraduate students. The product is used to demonstrate the fascinating and visually impressive phenomenon of luminescence thermochromism: exposed to long-wave UV light, the…

  10. Leaching of iodide (I(-)) and iodate (IO3(-)) anions from synthetic layered double hydroxide materials.

    PubMed

    Theiss, Frederick L; Ayoko, Godwin A; Frost, Ray L

    2016-09-15

    Several studies have previously demonstrated that layered double hydroxides (LDHs) show considerable potential for the adsorption of radioiodine from aqueous solution; however, few studies have demonstrated that these materials are able to store radioactive (131)I for an acceptable period. The leaching of iodide (I(-)) and iodate (IO3(-)) form Mg/Al LDHs has been carried out. Contact time appeared to be a more significant variable for the leaching of iodate (IO3(-)) compared to that of iodide (I(-)). Experimental results are fitted to the pseudo second order model, suggesting that diffusion is likely to be the rate-limiting step. The presence of carbonate in the leaching solution appeared to significantly increase the leaching of iodide (I(-)) as did the presence of chloride to a lesser extent. The maximum amount of iodate (IO3(-)) leached using ultrapure water as the leaching solution was 21% of the iodate (IO3(-)) originally present. The corresponding result for iodide (I(-)) was even lower at 3%.

  11. A portable multi-syringe flow system for spectrofluorimetric determination of iodide in seawater.

    PubMed

    Frizzarin, Rejane M; Aguado, Enrique; Portugal, Lindomar A; Moreno, Daniel; Estela, José M; Rocha, Fábio R P; Cerdà, Victor

    2015-11-01

    A miniaturized analyzer encompassing a poly(methyl methacrylate) chip with integrated spectrofluorimetric detection and solutions propelling by a multi-syringe module is proposed. Iodide was determined through its catalytic effect on the reaction between Ce(IV) and As(III). Matrix isopotential synchronous fluorescence was explored to set the excitation and emission wavelengths. A two-level full factorial design allowed to evaluate the significance of variables (Ce(IV), As(III) and H2SO4 concentrations) and their interaction effects in the experimental domain. A Doehlert Matrix was applied to identify the critical values. The optimized procedure showed a linear response from 1 to 100 μg L(-1) (S=53.7+2.61C, in which S is the net fluorescence and C is iodide concentration in μg L(-1)). Detection limit, coefficient of variation (n=6) and sampling rate were estimated at 0.3 μg L(-1), 0.8% and 20 h(-1), respectively. Recoveries within 90-117% were estimated for iodide spiked to seawater samples. The proposed procedure stands out because of the portability, robustness, and simplicity for in-field analysis of iodide in seawater. PMID:26452941

  12. The Reaction between Iron(II) Iodide and Potassium Dichromate(VI) in Acidified Aqueous Solution

    ERIC Educational Resources Information Center

    Talbot, Christopher

    2013-01-01

    This "Science note" teaching lesson explores the possible reaction between the ions in a reaction mixture consisting of iron(II) iodide and potassium dichromate(VI) in acidified aqueous solution. The electrode potentials will be used to deduce any spontaneous reactions under standard thermodynamic conditions (298 K, 1 bar (approximately…

  13. Ortho C-H Acylation of Aryl Iodides by Palladium/Norbornene Catalysis.

    PubMed

    Dong, Zhe; Wang, Jianchun; Ren, Zhi; Dong, Guangbin

    2015-10-19

    Reported herein is a palladium/norbornene-catalyzed ortho-arene acylation of aryl iodides by a Catellani-type C-H functionalization. This transformation is enabled by isopropyl carbonate anhydrides, which serve as both an acyl cation equivalent and a hydride source.

  14. Transport properties of iodide in a sandy aquifer: Hydrogeological modelling and field tracer tests

    NASA Astrophysics Data System (ADS)

    Razafindratsima, Stephen; Péron, Olivier; Piscitelli, Anne; Gégout, Claire; Schneider, Vincent; Barbecot, Florent; Giffaut, Eric; Robinet, Jean-Charles; Le Cointe, Pierre; Montavon, Gilles

    2015-01-01

    The release of radioactive iodine into geological media from nuclear waste disposal is an issue that has to be considered since iodine is a biophilic element. 129I is, with 99Tc, one of the two long-lived radionuclides that have the highest mobility in radioactive waste disposal. Within this context, iodide retardation is still a matter of debate. A low value of the retardation factor is generally accepted in soils without organic matter, but the possibility for sorption cannot be completely ruled out. Since isotopic exchange with naturally occurring iodine is one of the main potential sorption mechanisms, site-specific retention parameters are needed. In the present paper, we study iodide transport in a sandy aquifer. A hydrogeological model was built to fit deuterium, bromide and iodide breakthrough data from in situ tracer test experiments. Within the precision range of the fitting, iodide is excluded from 2.5% of the effective porosity by anionic exclusion and presents a field retention factor (Kd) lower than 0.025 L/kg.

  15. Activation of lactoperoxidase by heme-linked protonation and heme-independent iodide binding.

    PubMed

    Toyama, Akira; Tominaga, Aya; Inoue, Tatsuo; Takeuchi, Hideo

    2010-01-01

    Lactoperoxidase (LPO), a mammalian secretory heme peroxidase, catalyzes the oxidation of thiocyanate by hydrogen peroxide to produce hypothiocyanate, an antibacterial agent. Although LPO is known to be activated at acidic pH and in the presence of iodide, the structural basis of the activation is not well understood. We have examined the effects of pH and iodide concentration on the catalytic activity and the structure of LPO. Electrochemical and colorimetric assays have shown that the catalytic activity is maximized at pH 4.5. The heme Soret absorption band exhibits a small red-shift at pH 5.0 upon acidification, which is ascribable to a structural transition from a neutral to an acidic form. Resonance Raman spectra suggest that the heme porphyrin core is slightly contracted and the Fe-His bond is strengthened in the acidic form compared to the neutral form. The structural change of LPO upon activation at acidic pH is similar to that observed for myeloperoxidase, another mammalian heme peroxidase, upon activation at neutral pH. Binding of iodide enhances the catalytic activity of LPO without affecting either the optimum pH of activity or the heme structure, implying that the iodide binding occurs at a protein site away from the heme-linked protonation site.

  16. Mitigating 1,3-dichloropropene, chloropicrin, and methyl iodide emissions from fumigated soil with reactive film

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Implicated as a stratospheric ozone-depleting compound, methyl bromide (MeBr) is being phased out despite being considered to be the most effective soil fumigant. Its alternatives, i.e., 1,3-dichloropropene (1,3-D, which includes cis- and trans- isomers), chloropicrin (CP) and methyl iodide (MeI), h...

  17. Phase partitioning, retention kinetics, and leaching of fumigant methyl iodide in agricultural soils

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Although it is not currently being sold in the USA, the recent US registration of the fumigant methyl iodide has led to an increased interest in its environmental fate and transport. Although some work has now considered its volatile emissions from soil, there remains a lack of experimental data reg...

  18. Electron stimulated reactions of methyl iodide coadsorbed with amorphous solid water

    SciTech Connect

    Perry, C. C.; Faradzhev, N. S.; Madey, T. E.; Fairbrother, D. H.

    2007-05-28

    The electron stimulated reactions of methyl iodide (MeI) adsorbed on and suspended within amorphous solid water (ice) were studied using a combination of postirradiation temperature programmed desorption and reflection absorption infrared spectroscopy. For MeI adsorbed on top of amorphous solid water (ice), electron beam irradiation is responsible for both structural and chemical transformations within the overlayer. Electron stimulated reactions of MeI result principally in the formation of methyl radicals and solvated iodide anions. The cross section for electron stimulated decomposition of MeI is comparable to the gas phase value and is only weakly dependent upon the local environment. For both adsorbed MeI and suspended MeI, reactions of methyl radicals within MeI clusters lead to the formation of ethane, ethyl iodide, and diiodomethane. In contrast, reactions between the products of methyl iodide and water dissociation are responsible for the formation of methanol and carbon dioxide. Methane, formed as a result of reactions between methyl radicals and either parent MeI molecules or hydrogen atoms, is also observed. The product distribution is found to depend on the film's initial chemical composition as well as the electron fluence. Results from this study highlight the similarities in the carbon-containing products formed when monohalomethanes coadsorbed with amorphous solid water are irradiated by either electrons or photons.

  19. Corrosion of iron by iodide-oxidizing bacteria isolated from brine in an iodine production facility.

    PubMed

    Wakai, Satoshi; Ito, Kimio; Iino, Takao; Tomoe, Yasuyoshi; Mori, Koji; Harayama, Shigeaki

    2014-10-01

    Elemental iodine is produced in Japan from underground brine (fossil salt water). Carbon steel pipes in an iodine production facility at Chiba, Japan, for brine conveyance were found to corrode more rapidly than those in other facilities. The corroding activity of iodide-containing brine from the facility was examined by immersing carbon steel coupons in "native" and "filter-sterilized" brine samples. The dissolution of iron from the coupons immersed in native brine was threefold to fourfold higher than that in the filter-sterilized brine. Denaturing gradient gel electrophoresis analyses revealed that iodide-oxidizing bacteria (IOBs) were predominant in the coupon-containing native brine samples. IOBs were also detected in a corrosion deposit on the inner surface of a corroded pipe. These results strongly suggested the involvement of IOBs in the corrosion of the carbon steel pipes. Of the six bacterial strains isolated from a brine sample, four were capable of oxidizing iodide ion (I(-)) into molecular iodine (I(2)), and these strains were further phylogenetically classified into two groups. The iron-corroding activity of each of the isolates from the two groups was examined. Both strains corroded iron in the presence of potassium iodide in a concentration-dependent manner. This is the first report providing direct evidence that IOBs are involved in iron corrosion. Further, possible mechanisms by which IOBs corrode iron are discussed.

  20. The In-Gap Electronic State Spectrum of Methylammonium Lead Iodide Single-Crystal Perovskites.

    PubMed

    Adinolfi, Valerio; Yuan, Mingjian; Comin, Riccardo; Thibau, Emmanuel S; Shi, Dong; Saidaminov, Makhsud I; Kanjanaboos, Pongsakorn; Kopilovic, Damir; Hoogland, Sjoerd; Lu, Zheng-Hong; Bakr, Osman M; Sargent, Edward H

    2016-05-01

    The density of trap states within the bandgap of methylammonium lead iodide single crystals is investigated. Defect states close to both the conduction and valence bands are probed. Additionally, a comprehensive electronic characterization of crystals is carried out, including measurements of the electron and hole mobility, and the energy landscape (band diagram) at the surface.