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Sample records for cationic silver clusters

  1. Pulsed EPR for studying silver clusters

    Energy Technology Data Exchange (ETDEWEB)

    Michalik, J.; Wasowicz, T.; Sadlo, J. [Institute of Nuclear Chemistry and Technology, Warsaw (Poland); Reijerse, E.J. [Katholieke Univ., Nijmegen (Netherlands). Dept. of Molecular Spectroscopy; Kevan, L. [Texas Univ., Houston, TX (United States). Dept. of Chemistry

    1996-01-01

    The cationic silver clusters of different nuclearity have been produced by radiolysis of zeolite A and SAPO molecular sieves containing Ag{sup +} as exchangeable cations. The pulsed EPR spectroscopy has been applied for studying the local environment of silver cluster in order to understand the mechanism of cluster formation and stabilization. the electron spin echo modulation (ESEM) results on Ag{sub 6}{sup n+} cluster in dehydration zeolite A indicate that the hexameric silver is stabilized only in sodalite cages which are surrounded by {alpha}-cages containing no water molecules. Trimeric silver clusters formed in hydrated A zeolites strongly interact with water, thus the paramagnetic center can be considered as a cluster-water adduct. In SAPO-molecular sieves, silver clusters are formed only in the presence of adsorbed alcohol molecules. From ESEM it is determined that Ag{sub 4}{sup n+} in SAPO-42 is stabilized in {alpha} cages, where it is directly coordinated by two methanol molecules. Dimeric silver, Ag{sub 2}{sup +} in SAPO-5 and SAPO-11 is located in 6-ring channels and interacts with three CH{sub 3}OH molecules, each in different 10 ring or 12 ring channels. The differences of Ag{sub 2}{sup +} stability in SAPO-5 and SAPO-11 are also discussed. (Author).

  2. Pulsed EPR for studying silver clusters

    Science.gov (United States)

    Michalik, J.; Wasowicz, T.; Sadlo, J.; Reijerse, E. J.; Kevan, L.

    1996-01-01

    The cationic silver clusters of different nuclearity have been produced by radiolysis of zeolite A and SAPO molecular sieves containing Ag + as exchangeable cations. The pulsed EPR spectroscopy has been applied for studying the local environment of silver cluster in order to understand the mechanism of cluster formation and stabilization. The electron spin echo modulation (ESEM) results on Ag 6n+ cluster in dehydration zeolite A indicate that the hexameric silver is stabilized only in sodalite cages which are surrounded by α-cages containing no water molecules. Trimeric silver clusters formed in hydrated A zeolites strongly interact with water, thus the paramagnetic center can be considered as a cluster-water adduct. In SAPO-molecular sieves, silver clusters are formed only in the presence of adsorbed alcohol molecules. From ESEM it is determined that Ag 4n+ in SAPO-42 is stabilized in α-cages, where it is directly coordinated by two methanol molecules. Dimeric silver, Ag 2+ in SAPO-5 and SAPO-11 is located in 6-ring channels and interacts with three CH 3OH molecules, each in different 10-ring or 12-ring channels. The differences of Ag 2+ stability in SAPO-5 and SAPO-11 are also discussed.

  3. The interaction of gold and silver nanoparticles with a range of anionic and cationic dyes

    OpenAIRE

    Kitching, H; Kenyon, A. J.; Parkin, I. P.

    2014-01-01

    We describe the synthesis of charge-stabilised gold and silver nanoparticles by a modified Turkevich method and their interaction with a selection of cationic and anionic dyes. It was found that gold nanoparticles interact strongly with cationic dyes and in some cases enhanced absorption was observed by UV-visible spectroscopy. It is also shown that addition of cationic dyes to gold nanoparticles triggers aggregation of the nanoparticles into large, micrometre-scale clusters. Simultaneous fra...

  4. Tuning Properties in Silver Clusters

    KAUST Repository

    Joshi, Chakra P

    2015-07-09

    The properties of Ag nanoclusters are not as well understood as those of their more precious Au cousins. However, a recent surge in the exploration of strategies to tune the physicochemical characteristics of Ag clusters addresses this imbalance, leading to new insights into their optical, luminescence, crystal habit, metal-core, ligand-shell and environmental properties. In this Perspective, we provide an overview of the latest strategies along with a brief introduction of the theoretical framework necessary to understand the properties of silver nanoclusters and the basis for their tuning. The advances in cluster research and the future prospects presented in this Perspective will eventually guide the next large systematic study of nanoclusters, resulting in a single collection of data similar to the periodic table of elements.

  5. Anaerobic Toxicity of Cationic Silver Nanoparticles

    Science.gov (United States)

    The microbial toxicity of silver nanoparticles (AgNPs) stabilized with different capping agents was compared to that of Ag+ under anaerobic conditions. Three AgNPs were investigated: (1) negatively charged citrate-coated AgNPs (citrate-AgNPs), (2) minimally charged p...

  6. Water adsorption on free cobalt cluster cations

    NARCIS (Netherlands)

    D.M. Kiawi; J.M. Bakker; J. Oomens; W.J. Buma; Z. Jamshidi; L. Visscher; L.B.F.M. Waters

    2015-01-01

    Cationic cobalt clusters complexed with water Con+-​H2O (n = 6-​20) are produced through laser ablation and investigated via IR multiple photon dissocn. (IR-​MPD) spectroscopy in the 200-​1700 cm-​1 spectral range. All spectra exhibit a resonance close to the 1595 cm-​1 frequency of the free water b

  7. Plasmon enhanced silver quantum cluster fluorescence for biochemical applications

    DEFF Research Database (Denmark)

    Bernard, S.; Kutter, J.P.; Mogensen, Klaus Bo

    2014-01-01

    Fluorescence microscopy of individual silver quantum clusters on the surface of silver nanoparticles reveals strong photoactivated emission under blue light excitation [1-4]. In this work, silver nanoparticles are produced by annealing silver thin films deposited on a glass substrate and silver q...

  8. DNA-Protected Silver Clusters for Nanophotonics

    Directory of Open Access Journals (Sweden)

    Elisabeth Gwinn

    2015-02-01

    Full Text Available DNA-protected silver clusters (AgN-DNA possess unique fluorescence properties that depend on the specific DNA template that stabilizes the cluster. They exhibit peak emission wavelengths that range across the visible and near-IR spectrum. This wide color palette, combined with low toxicity, high fluorescence quantum yields of some clusters, low synthesis costs, small cluster sizes and compatibility with DNA are enabling many applications that employ AgN-DNA. Here we review what is known about the underlying composition and structure of AgN-DNA, and how these relate to the optical properties of these fascinating, hybrid biomolecule-metal cluster nanomaterials. We place AgN-DNA in the general context of ligand-stabilized metal clusters and compare their properties to those of other noble metal clusters stabilized by small molecule ligands. The methods used to isolate pure AgN-DNA for analysis of composition and for studies of solution and single-emitter optical properties are discussed. We give a brief overview of structurally sensitive chiroptical studies, both theoretical and experimental, and review experiments on bringing silver clusters of distinct size and color into nanoscale DNA assemblies. Progress towards using DNA scaffolds to assemble multi-cluster arrays is also reviewed.

  9. Magnetic Properties of Iron Clusters in Silver

    Energy Technology Data Exchange (ETDEWEB)

    Elzain, M., E-mail: elzain@squ.edu.om; Al Rawas, A.; Yousif, A.; Gismelseed, A.; Rais, A.; Al-Omari, I.; Bouziane, K. [College of Science, Department of Physics (Oman); Widatallah, H. [Khartoum University, Department of Physics, Faculty of Science (Sudan)

    2004-12-15

    The discrete variational method is used to study the effect of interactions of iron impurities on the magnetic moments, hyperfine fields and isomer shifts at iron sites in silver. We study small clusters of iron atoms as they grow to form FCC phase that is coherent with the silver lattice. The effects of the lattice relaxation and the ferromagnetic and antiferromagnetic couplings are also considered. When Fe atoms congregate around a central Fe atom in an FCC arrangement under ferromagnetic coupling, the local magnetic moment and the contact charge density at the central atom hardly change as the cluster builds up, whereas the hyperfine field increases asymptotically as the number of Fe nearest neighbors increases. Introduction of antiferromagnetic coupling has minor effect on the local magnetic moments and isomer shifts, however it produces large reduction in the hyperfine field. The lattice relaxation of the surrounding Fe atoms towards a BCC phase around a central Fe atom leads to reduction in the magnetic moment accompanied by increase in the magnetic hyperfine field.

  10. Supported silver and copper clusters for photocatalysis

    Energy Technology Data Exchange (ETDEWEB)

    Popok, Vladimir; Barke, Ingo; Neubauer, Antje; Lochbrunner, Stefan; Meiwes-Broer, Karl-Heinz [Institut fuer Physik, Universitaet Rostock, Universitaetsplatz 3, 18051 Rostock (Germany)

    2011-07-01

    Nanometer-sized metal particles deposited onto surfaces are of significant interest for applications in catalysis. In the current study, nanoparticles of silver and copper in the size range from ca. 5 to 18 nm were formed using arc-discharge and magnetron sputtering cluster ion sources and deposited on silica glass substrates. The prepared cluster-assembled samples have been studied in order to increase the efficiency of existing catalytic schemes for hydrogen production, which is of high practical importance. In particular, Ir photosensitizers (PS) in combination with palladium, platinum or iron catalysts are known to be promising systems for reduction of aqueous protons to hydrogen. We deposited the PS on cluster-covered samples and studied their optical properties. It is found that in presence of metal clusters the ligand-centered optical transitions of the PS are significantly increased accompanied by a change of the photoluminescence. These findings indicate considerable effect of the metal nanoparticles on the electronic structure of the PS, a fact that might be of relevance for the improvement of photo-catalytic reactions.

  11. Blackbody-induced radiative dissociation of cationic SF 6 clusters

    DEFF Research Database (Denmark)

    Toker, Jonathan; Rahinov, I.; Schwalm, D.;

    2012-01-01

    The stability of cationic SF5+(SF6)n−1 clusters was investigated by measuring their blackbody-induced radiative dissociation (BIRD) rates. The clusters were produced in a supersonic expansion ion source and stored in an electrostatic ion-beam trap at room temperature, where their abundances...... and lifetimes were measured. Using the “master equation” approach, relative binding energies of an SF6 unit in the clusters could be extracted from the storage-time dependence of the survival probabilities. The results allow for a deeper insight into the effect of a localized charge on the structure...... and stability of SF6-based clusters....

  12. Structure, spectra and dynamics of alkali cation microhydration clusters

    OpenAIRE

    Schulz, Franziska

    2005-01-01

    The main focus of this work was the theoretical investigation of alkali cation microhydration clusters with sodium, potassium, and caesium as central ion and up to 24 water molecules per cluster. Structures were obtained applying global geometry optimisation, using a specialised version of genetic algorithms and the common TIP4P/OPLS model potential. The global and most important local minimum energy structures have been investigated and the results obtained constitute a first complete and sy...

  13. THEORETICAL STUDY ON THE INTERACTION BETWEEN XENON AND POSITIVE SILVER CLUSTERS IN GAS PHASE AND ON THE (001) CHABAZITE SURFACE

    Energy Technology Data Exchange (ETDEWEB)

    Hunter, D.

    2009-03-16

    A systematic study on the adsorption of xenon on silver clusters in the gas phase and on the (001) surface of silver-exchanged chabazite is reported. Density functional theory at the B3LYP level with the cluster model was employed. The results indicate that the dominant part of the binding is the {sigma} donation, which is the charge transfer from the 5p orbital of Xe to the 5s orbital of Ag and is not the previously suggested d{sub {pi}}-d{sub {pi}} back-donation. A correlation between the binding energy and the degree of {sigma} donation is found. Xenon was found to bind strongly to silver cluster cations and not to neutral ones. The binding strength decreases as the cluster size increases for both cases, clusters in the gas-phase and on the chabazite surface. The Ag{sup +} cation is the strongest binding site for xenon both in gas phase and on the chabazite surface with the binding energies of 73.9 and 14.5 kJ/mol, respectively. The results also suggest that the smaller silver clusters contribute to the negative chemical shifts observed in the {sup 129}Xe NMR spectra in experiments.

  14. Reaction between sulfur dioxide and iron oxide cationic clusters

    Institute of Scientific and Technical Information of China (English)

    YIN Shi; HE ShengGui; HE ShengGui; GE MaoFa; GE MaoFa

    2009-01-01

    The reactivity of sulfur dioxide (SO_2) molecules toward iron oxide cationic clusters (Fe_mO_n~+) is studied by a homemade time-of-flight mass spectrometer coupled with a laser ablation/supersonic expansion cluster source and a fast flow reactor.The association products Fe_mO_nSO_2~+ can be observed for most of the clusters.The interesting result is that the cooperation effect of SO_2 and water is in favor of the adsorption of gas phase water on specific scale iron oxide clusters (Fe_2O_2~+ and Fe_3O_3~+).The reactivity information obtained may be useful to investigate atmospheric heterogeneous chemistry of related systems.

  15. Supported silver clusters as nanoplasmonic transducers for protein sensing

    DEFF Research Database (Denmark)

    Fojan, Peter; Hanif, Muhammad; Bartling, Stephen;

    2015-01-01

    to quartz and functionalization of cluster surfaces for antibody coupling are the key issues for cluster stability and protein detection. Focus was put on these tasks and the processes have been optimised. In particular, conditions for coupling of the antibodies to the clusters are developed providing...... an enhancement of the plasmon absorption band used for the detection. Atomic force microscopy study allows to suggest that immobilisation of antibodies on silver clusters has been achieved, thus giving a possibility to incubate and detect an antigen of interest. Hence, by applying the developed preparation...

  16. Formation and characterization of thioglycolic acid-silver cluster complexes.

    Science.gov (United States)

    Bellina, Bruno; Antoine, Rodolphe; Broyer, Michel; Gell, Lars; Sanader, Željka; Mitrić, Roland; Bonačić-Koutecký, Vlasta; Dugourd, Philippe

    2013-06-21

    Gas phase reactivity observed in an ion trap was used to produce silver clusters protected with thioglycolic acid. Fragmentation pathways as well as optical properties were explored experimentally and theoretically. Sequential losses of SCH2 and CO2 in the ion trap lead to redox reactions with charge transfers between the metal part and the carboxylate and thiolate groups. This allows us to control the number of electrons in the metallic subunit and thus optical properties of the complexes. The presented formation process can be used as a prototype for tuning optical and chemical properties of ligated metal clusters by varying the number of confined electrons within the metallic subunit.

  17. Coalescence of silver clusters by immersion in diluted HF solution

    Energy Technology Data Exchange (ETDEWEB)

    Milazzo, R. G.; Mio, A. M.; D’Arrigo, G.; Spinella, C. [CNR-IMM Institute for Microelectronics and Microsystems, I-95121 Catania (Italy); Grimaldi, M. G. [Department of Physics and Astronomy, Università di Catania, I-95123 Catania (Italy); MATIS IMM-CNR, I-95123 Catania (Italy); Rimini, E. [CNR-IMM Institute for Microelectronics and Microsystems, I-95121 Catania (Italy); Department of Physics and Astronomy, Università di Catania, I-95123 Catania (Italy)

    2015-07-14

    The galvanic displacement deposition of silver on H-terminated Si (100) in the time scale of seconds is instantaneous and characterized by a cluster density of 10{sup 11}-10{sup 12} cm{sup −2}. The amount of deposited Ag follows a t{sup 1/2} dependence in agreement with a Cottrell diffusion limited mechanism. At the same time, during the deposition, the cluster density reduces by a factor 5. This behavior is in contrast with the assumption of immobile clusters. We show in the present work that coalescence and aggregation occur also in the samples immersed in the diluted hydrofluoric acid (HF) solution without the presence of Ag{sup +}. Clusters agglomerate according to a process of dynamic coalescence, typical of colloids, followed by atomic redistribution at the contact regions with the generation of multiple internal twins and stacking-faults. The normalized size distributions in terms of r/r{sub mean} follow also the prediction of the Smoluchowski ripening mechanism. No variation of the cluster density occurs for samples immersed in pure H{sub 2}O solution. The different behavior might be associated to the strong attraction of clusters to oxide-terminated Si surface in presence of water. The silver clusters are instead weakly bound to hydrophobic H-terminated Si in presence of HF. HF causes then the detachment of clusters and a random movement on the silicon surface with mobility of about 10{sup −13} cm{sup 2}/s. Attractive interaction (probably van der Waals) among particles promotes coarsening.

  18. Cluster Plasmonics: Dielectric and Shape Effects on DNA-Stabilized Silver Clusters.

    Science.gov (United States)

    Copp, Stacy M; Schultz, Danielle; Swasey, Steven M; Faris, Alexis; Gwinn, Elisabeth G

    2016-06-01

    This work investigates the effects of dielectric environment and cluster shape on electronic excitations of fluorescent DNA-stabilized silver clusters, AgN-DNA. We first establish that the longitudinal plasmon wavelengths predicted by classical Mie-Gans (MG) theory agree with previous quantum calculations for excitation wavelengths of linear silver atom chains, even for clusters of just a few atoms. Application of MG theory to AgN-DNA with 400-850 nm cluster excitation wavelengths indicates that these clusters are characterized by a collective excitation process and suggests effective cluster thicknesses of ∼2 silver atoms and aspect ratios of 1.5 to 5. To investigate sensitivity to the surrounding medium, we measure the wavelength shifts produced by addition of glycerol. These are smaller than reported for much larger gold nanoparticles but easily detectable due to narrower line widths, suggesting that AgN-DNA may have potential for fluorescence-reported changes in dielectric environment at length scales of ∼1 nm.

  19. Structures of tin cluster cations Sn3+ to Sn15+

    Science.gov (United States)

    Drebov, Nedko; Oger, Esther; Rapps, Thomas; Kelting, Rebecca; Schooss, Detlef; Weis, Patrick; Kappes, Manfred M.; Ahlrichs, Reinhart

    2010-12-01

    We employ a combination of ion mobility measurements and an unbiased systematic structure search with density functional theory methods to study structure and energetics of gas phase tin cluster cations, {Snn}^+, in the range of n = 3-15. For {Sn_{13}}^+ we also carry out trapped ion electron diffraction measurements to ascertain the results obtained by the other procedures. The structures for the smaller systems are most easily described by idealized point group symmetries, although they are all Jahn-Teller distorted: D_{3h} (trigonal bipyramid), D_{4h} (octahedron), D_{5h} (pentagonal bipyramid) for n = 5, 6, and 7. For the larger systems we find capped D_{5h} for {Sn8}^+ and {Sn9}^+, D_{3h} (tricapped trigonal prism) and D_{4d} (bicapped squared antiprism) plus adatoms for n = 10, 11, 14, and 15. A centered icosahedron with a peripheral atom removed is the dominant motif in {Sn_{12}}^+. For {Sn_{13}}^+ the calculations predict a family of virtually isoenergetic isomers, an icosahedron and slightly distorted icosahedra, which are about 0.25 eV below two C_1 structures. The experiments indicate the presence of two structures, one from the I_h family and a prolate C_1 isomer based on fused deltahedral moieties.

  20. Supported quantum clusters of silver as enhanced catalysts for reduction

    Science.gov (United States)

    Leelavathi, Annamalai; Bhaskara Rao, Thumu Udaya; Pradeep, Thalappil

    2011-12-01

    Quantum clusters (QCs) of silver such as Ag7(H2MSA)7, Ag8(H2MSA)8 (H2MSA, mercaptosuccinic acid) were synthesized by the interfacial etching of Ag nanoparticle precursors and were loaded on metal oxide supports to prepare active catalysts. The supported clusters were characterized using high resolution transmission electron microscopy, scanning electron microscopy, X-ray photoelectron spectroscopy, and laser desorption ionization mass spectrometry. We used the conversion of nitro group to amino group as a model reaction to study the catalytic reduction activity of the QCs. Various aromatic nitro compounds, namely, 3-nitrophenol (3-np), 4-nitrophenol (4-np), 3-nitroaniline (3-na), and 4-nitroaniline (4-na) were used as substrates. Products were confirmed using UV-visible spectroscopy and electrospray ionization mass spectrometry. The supported QCs remained active and were reused several times after separation. The rate constant suggested that the reaction followed pseudo-first-order kinetics. The turn-over frequency was 1.87 s-1 per cluster for the reduction of 4-np at 35°C. Among the substrates investigated, the kinetics followed the order, SiO2 > TiO2 > Fe2O3 > Al2O3.

  1. Supported quantum clusters of silver as enhanced catalysts for reduction

    Directory of Open Access Journals (Sweden)

    Leelavathi Annamalai

    2011-01-01

    Full Text Available Abstract Quantum clusters (QCs of silver such as Ag7(H2MSA7, Ag8(H2MSA8 (H2MSA, mercaptosuccinic acid were synthesized by the interfacial etching of Ag nanoparticle precursors and were loaded on metal oxide supports to prepare active catalysts. The supported clusters were characterized using high resolution transmission electron microscopy, scanning electron microscopy, X-ray photoelectron spectroscopy, and laser desorption ionization mass spectrometry. We used the conversion of nitro group to amino group as a model reaction to study the catalytic reduction activity of the QCs. Various aromatic nitro compounds, namely, 3-nitrophenol (3-np, 4-nitrophenol (4-np, 3-nitroaniline (3-na, and 4-nitroaniline (4-na were used as substrates. Products were confirmed using UV-visible spectroscopy and electrospray ionization mass spectrometry. The supported QCs remained active and were reused several times after separation. The rate constant suggested that the reaction followed pseudo-first-order kinetics. The turn-over frequency was 1.87 s-1 per cluster for the reduction of 4-np at 35°C. Among the substrates investigated, the kinetics followed the order, SiO2 > TiO2 > Fe2O3 > Al2O3.

  2. Carbon monoxide adsorption on neutral and cationic vanadium doped gold clusters

    OpenAIRE

    Le, Hai Thuy; Lang, Sandra M; de Haeck, Jorg; Lievens, Peter; Janssens, Ewald

    2012-01-01

    The effect of a single vanadium dopant atom on the reactivity of small gold clusters is studied in the gas phase. In particular we investigated carbon monoxide adsorption on vanadium doped gold clusters using a low-pressure collision cell. Employing this technique the reactivity of both neutral and cationic clusters was studied under the same experimental conditions. Analysis of the kinetic data as a function of the pressure in the reaction cell shows that the reaction mechanism is composed o...

  3. Molecular adsorption of H2 on small cationic nickel clusters

    NARCIS (Netherlands)

    Swart, I.; Gruene, P.; Fielicke, A.; Meijer, G.; Weckhuysen, B.M.; de Groot, F.M.F.

    2008-01-01

    The adsorption of H2 on metal clusters is of interest in several fields, including metallurgy, catalysis and hydrogen storage. Hydrogen interacting with small Ni clusters is of special interest, as Ni is widely used as a hydrogenation catalyst. In general, reactions of H2 with extended Ni surfaces a

  4. Thermochromic luminescent nest-like silver thiolate cluster.

    Science.gov (United States)

    Li, Bo; Huang, Ren-Wu; Qin, Jian-Hua; Zang, Shuang-Quan; Gao, Guang-Gang; Hou, Hong-Wei; Mak, Thomas C W

    2014-09-22

    A novel discrete open high-nuclearity nest-like silver thiolate cluster complex, [Ag33 S3 (StBu)16 (CF3 COO)9 (NO3 )(CH3 CN)2 ](NO3 ) (1), has been isolated with nitrate and S(2-) anions acting as structure-directing templates. Its similar nest-like structure has been assembled into an extended layer [Ag31 S3 (StBu)16 (NO3 )9 ]n (2) by adjustment of auxiliary ligand. More interestingly, both complexes exhibit temperature-dependent luminescence of high sensitivity with a large fluorescence enhancement (12-fold for 1, 21-fold for 2), which can be easily recognized by the naked-eye (dramatic red-shift Δ=104 nm for 1, larger Δ=113 nm for 2 at 77 K compared to those at 298 K). The correlation between luminescent thermochromism and temperature-dependent variation of the coordination modes of template NO3 (-) anion, Ag⋅⋅⋅S and Ag⋅⋅⋅Ag distances are also elucidated through variable-temperature single-crystal X-ray crystal structure (VT-SCXRD) analyses. PMID:25124942

  5. Simulation of molecular dynamics of silver subcritical nuclei and crystal clusters during solidification

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Molecular dynamics simulation is carried out to investigate the effects of cooling rate on the final configurations of silver after rapid solidification. The cooling rate for the formation of a silver amorphous phase is determined by analyzing its pair distribution function, H-A bond index, and the largest crystal cluster. Further, the equilibrium structures of the subcritical nuclei and crystal clusters are studied. The results show that the solidified microstructure is composed of a mixture of crystal clusters and amorphous phases at a certain cooling rate range. The size of the largest crystal cluster decreases with the increasing cooling rate, and it completely disappears when the cooling rate exceeds a critical value. The structures of the subcritical nuclei and the largest crystal cluster are composed of lamellar structures of fcc and hcp atoms, indicating that the lamellar structure of fcc and hcp atoms in the silver crystal originates from nucleation, and not from the growth of crystals.

  6. Tuning the energetics and tailoring the optical properties of silver clusters confined in zeolites

    Science.gov (United States)

    Fenwick, Oliver; Coutiño-Gonzalez, Eduardo; Grandjean, Didier; Baekelant, Wouter; Richard, Fanny; Bonacchi, Sara; de Vos, Dirk; Lievens, Peter; Roeffaers, Maarten; Hofkens, Johan; Samorì, Paolo

    2016-09-01

    The integration of metal atoms and clusters in well-defined dielectric cavities is a powerful strategy to impart new properties to them that depend on the size and geometry of the confined space as well as on metal-host electrostatic interactions. Here, we unravel the dependence of the electronic properties of metal clusters on space confinement by studying the ionization potential of silver clusters embedded in four different zeolite environments over a range of silver concentrations. Extensive characterization reveals a strong influence of silver loading and host environment on the cluster ionization potential, which is also correlated to the cluster’s optical and structural properties. Through fine-tuning of the zeolite host environment, we demonstrate photoluminescence quantum yields approaching unity. This work extends our understanding of structure-property relationships of small metal clusters and applies this understanding to develop highly photoluminescent materials with potential applications in optoelectronics and bioimaging.

  7. Near-infrared silver cluster optically signaling oligonucleotide hybridization and assembling two DNA hosts.

    Science.gov (United States)

    Petty, Jeffrey T; Nicholson, David A; Sergev, Orlin O; Graham, Stuart K

    2014-09-16

    Silver clusters with ~10 atoms form within DNA strands, and the conjugates are chemical sensors. The DNA host hybridizes with short oligonucleotides, and the cluster moieties optically respond to these analytes. Our studies focus on how the cluster adducts perturb the structure of their DNA hosts. Our sensor is comprised of an oligonucleotide with two components: a 5'-cluster domain that complexes silver clusters and a 3'-recognition site that hybridizes with a target oligonucleotide. The single-stranded sensor encapsulates an ~11 silver atom cluster with violet absorption at 400 nm and with minimal emission. The recognition site hybridizes with complementary oligonucleotides, and the violet cluster converts to an emissive near-infrared cluster with absorption at 730 nm. Our key finding is that the near-infrared cluster coordinates two of its hybridized hosts. The resulting tertiary structure was investigated using intermolecular and intramolecular variants of the same dimer. The intermolecular dimer assembles in concentrated (~5 μM) DNA solutions. Strand stoichiometries and orientations were chromatographically determined using thymine-modified complements that increase the overall conjugate size. The intramolecular dimer develops within a DNA scaffold that is founded on three linked duplexes. The high local cluster concentrations and relative strand arrangements again favor the antiparallel dimer for the near-infrared cluster. When the two monomeric DNA/violet cluster conjugates transform to one dimeric DNA/near-infrared conjugate, the DNA strands accumulate silver. We propose that these correlated changes in DNA structure and silver stoichiometry underlie the violet to near-infrared cluster transformation.

  8. Atomically precise arrays of fluorescent silver clusters: a modular approach for metal cluster photonics on DNA nanostructures.

    Science.gov (United States)

    Copp, Stacy M; Schultz, Danielle E; Swasey, Steven; Gwinn, Elisabeth G

    2015-03-24

    The remarkable precision that DNA scaffolds provide for arraying nanoscale optical elements enables optical phenomena that arise from interactions of metal nanoparticles, dye molecules, and quantum dots placed at nanoscale separations. However, control of ensemble optical properties has been limited by the difficulty of achieving uniform particle sizes and shapes. Ligand-stabilized metal clusters offer a route to atomically precise arrays that combine desirable attributes of both metals and molecules. Exploiting the unique advantages of the cluster regime requires techniques to realize controlled nanoscale placement of select cluster structures. Here we show that atomically monodisperse arrays of fluorescent, DNA-stabilized silver clusters can be realized on a prototypical scaffold, a DNA nanotube, with attachment sites separated by <10 nm. Cluster attachment is mediated by designed DNA linkers that enable isolation of specific clusters prior to assembly on nanotubes and preserve cluster structure and spectral purity after assembly. The modularity of this approach generalizes to silver clusters of diverse sizes and DNA scaffolds of many types. Thus, these silver cluster nano-optical elements, which themselves have colors selected by their particular DNA templating oligomer, bring unique dimensions of control and flexibility to the rapidly expanding field of nano-optics.

  9. Geometry optimization and structural distribution of silver clusters from Ag 170 to Ag 310

    Science.gov (United States)

    Shao, Xueguang; Yang, Xiaoli; Cai, Wensheng

    2008-07-01

    Silver clusters in the size range of 170-310 were optimized with a modified dynamic lattice search (DLS) method. Considering the computational complexity, only 21 clusters of several tens and magic numbers of atoms were investigated. The interaction of silver atoms is modeled by the Gupta potential. Results show that, between the 21 clusters, nine fcc and twelve m-Dh structures are obtained. Compared with the structures adopted by Ag 13 to Ag 160, the main motif is still m-Dh in the range of Ag 170-Ag 310, but the ratio of fcc structures obviously increases. It can, therefore, be deduced that the fcc motif is more stable for larger size silver clusters.

  10. Thermal desorption of oxygen from near-stoichiometric cationic vanadium oxide clusters

    Science.gov (United States)

    Kurokawa, Hodaka; Mafuné, Fumitaka

    2016-05-01

    Oxygen desorption from cationic vanadium oxide clusters, VnOm+ (n = 2-10), composed of a near-stoichiometric (n:m = 2:5) frame with excess oxygen attached was investigated in a thermal energy region by time-of-flight mass spectrometry and thermal desorption spectrometry. Oxygen molecules were observed to desorb from the clusters during heating. The activation energy for desorption was estimated from the temperature dependence of different clusters and exhibited an even-odd alternation with respect to the cluster size, n. This alternation can be explained in terms of oxidation states of the vanadium atoms.

  11. Photodissociation studies of calcium-coronene and calcium-pyrene cation clusters

    Science.gov (United States)

    Scott, A. C.; Buchanan, J. W.; Flynn, N. D.; Duncan, M. A.

    2008-01-01

    Gas-phase cluster cations combining calcium atoms and the polycyclic aromatic hydrocarbons (PAHs) coronene (C24H12) and pyrene (C16H10) are produced in a molecular beam using laser vaporization in a pulsed nozzle cluster source. Time-of-flight mass spectrometry reveals the formation of clusters of the form Cax(coronene)y+ for up to x = 4 and y = 3 and Cax(pyrene)y+ for up to x = 2 and y = 3. Mass-selected photodissociation studies show that the calcium cation is the most prominent fragment for each system. Photoinduced calcium carbide formation is prominent when two or more calcium atoms are present. Additionally, there is evidence that these clusters can form sandwich structures.

  12. Divalent Cation-Dependent Formation of Electrostatic PIP2 Clusters in Lipid Monolayers

    OpenAIRE

    Ellenbroek, WG Wouter; Wang, Y-H; Christian, DA; Discher, DE; Janmey, PA; Liu, AJ

    2011-01-01

    Polyphosphoinositides are among the most highly charged molecules in the cell membrane, and the most common polyphosphoinositide, phosphatidylinositol-4,5-bisphosphate (PIP2), is involved in many mechanical and biochemical processes in the cell membrane. Divalent cations such as calcium can cause clustering of the polyanionic PIP2, but the origin and strength of the effective attractions leading to clustering has been unclear. In addition, the question of whether the ion-mediated attractions ...

  13. Microhydrated aromatic cluster cations: Binding motifs of 4-aminobenzonitrile-(H2O)n cluster cations with n ≤ 4

    Science.gov (United States)

    Schmies, Matthias; Miyazaki, Mitsuhiko; Fujii, Masaaki; Dopfer, Otto

    2014-12-01

    Infrared photodissociation (IRPD) spectra of mass-selected 4-aminobenzonitrile-(water)n cluster cations, ABN+-(H2O)n with n ≤ 4, recorded in the N-H and O-H stretch ranges are analyzed by quantum chemical calculations at the M06-2X/aug-cc-pVTZ level to determine the evolution of the initial microhydration process of this bifunctional aromatic cation in its ground electronic state. IRPD spectra of cold clusters tagged with Ar and N2 display higher resolution and allow for a clear-cut structural assignment. The clusters are generated in an electron impact source, which generates predominantly the most stable isomers. The IRPD spectra are assigned to single isomers for n = 1-3. The preferred cluster growth begins with sequential hydration of the two acidic NH protons of the amino group (n = 1-2), which is followed by attachment of secondary H2O ligands hydrogen-bonded to the first-shell ligands (n = 3-4). These symmetric and branched structures are more stable than those with a cyclic H-bonded solvent network. Moreover, in the size range n ≤ 4 the formation of a solvent network stabilized by strong cooperative effects is favored over interior ion hydration which is destabilized by noncooperative effects. The potential of the ABN+-H2O dimer is characterized in detail and supports the cluster growth derived from the IRPD spectra. Although the N-H bonds are destabilized by stepwise microhydration, which is accompanied by increasing charge transfer from ABN+ to the solvent cluster, no proton transfer to the solvent is observed for n ≤ 4.

  14. Microhydrated aromatic cluster cations: Binding motifs of 4-aminobenzonitrile-(H{sub 2}O){sub n} cluster cations with n ≤ 4

    Energy Technology Data Exchange (ETDEWEB)

    Schmies, Matthias; Dopfer, Otto, E-mail: dopfer@physik.tu-berlin.de [Institut für Optik und Atomare Physik, Technische Universität Berlin, Hardenbergstr. 36, 10623 Berlin (Germany); Miyazaki, Mitsuhiko; Fujii, Masaaki [Chemical Resources Laboratory, Tokyo Institute of Technology, Yokohama 226-8503 (Japan)

    2014-12-07

    Infrared photodissociation (IRPD) spectra of mass-selected 4-aminobenzonitrile-(water){sub n} cluster cations, ABN{sup +}-(H{sub 2}O){sub n} with n ≤ 4, recorded in the N–H and O–H stretch ranges are analyzed by quantum chemical calculations at the M06-2X/aug-cc-pVTZ level to determine the evolution of the initial microhydration process of this bifunctional aromatic cation in its ground electronic state. IRPD spectra of cold clusters tagged with Ar and N{sub 2} display higher resolution and allow for a clear-cut structural assignment. The clusters are generated in an electron impact source, which generates predominantly the most stable isomers. The IRPD spectra are assigned to single isomers for n = 1–3. The preferred cluster growth begins with sequential hydration of the two acidic NH protons of the amino group (n = 1–2), which is followed by attachment of secondary H{sub 2}O ligands hydrogen-bonded to the first-shell ligands (n = 3–4). These symmetric and branched structures are more stable than those with a cyclic H-bonded solvent network. Moreover, in the size range n ≤ 4 the formation of a solvent network stabilized by strong cooperative effects is favored over interior ion hydration which is destabilized by noncooperative effects. The potential of the ABN{sup +}-H{sub 2}O dimer is characterized in detail and supports the cluster growth derived from the IRPD spectra. Although the N–H bonds are destabilized by stepwise microhydration, which is accompanied by increasing charge transfer from ABN{sup +} to the solvent cluster, no proton transfer to the solvent is observed for n ≤ 4.

  15. High reactivity of nanosized niobium oxide cluster cations in methane activation: A comparison with vanadium oxides

    International Nuclear Information System (INIS)

    The reactions between methane and niobium oxide cluster cations were studied and compared to those employing vanadium oxides. Hydrogen atom abstraction (HAA) reactions were identified over stoichiometric (Nb2O5)N+ clusters for N as large as 14 with a time-of-flight mass spectrometer. The reactivity of (Nb2O5)N+ clusters decreases as the N increases, and it is higher than that of (V 2O5)N+ for N ≥ 4. Theoretical studies were conducted on (Nb2O5)N+ (N = 2–6) by density functional calculations. HAA reactions on these clusters are all favorable thermodynamically and kinetically. The difference of the reactivity with respect to the cluster size and metal type (Nb vs V) was attributed to thermodynamics, kinetics, the electron capture ability, and the distribution of the unpaired spin density. Nanosized Nb oxide clusters show higher HAA reactivity than V oxides, indicating that niobia may serve as promising catalysts for practical methane conversion

  16. Poly (methyl methacrylate) Composites with Size-Selected Silver Nanoparticles Fabricated using Cluster Beam Technique

    DEFF Research Database (Denmark)

    Hanif, Muhammad; Juluri, Raghavendra Rao; Chirumamilla, Manohar;

    2016-01-01

    An embedment of metal nanoparticles of well-defined sizes in thin polymer films is of significant interest for a number of practical applications, in particular, for preparing materials with tunable plasmonic properties. In this article, we present a fabrication route for metal–polymer composites...... based on cluster beam technique allowing the formation of monocrystalline size-selected silver nanoparticles with a ±5–7% precision of diameter and controllable embedment into poly (methyl methacrylate). It is shown that the soft-landed silver clusters preserve almost spherical shape with a slight...

  17. Reactions of silver atoms and clusters in Ag-NaA zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Wasowicz, T.; Michalik, J. (Institute of Nuclear Chemistry and Technology, Warsaw (Poland))

    1991-01-01

    The agglomeration of silver in hydrated and dehydrated Ag-NaA zeolites gamma irradiated at 77 K has been studied by ESR. The agglomeration process is radiation-induced in hydrated samples whereas in dehydrated ones is initiated by thermal autoreduction. In the result different silver clusters are stabilized at room temperature, Ag{sub 3}{sup 2+}center dotcenter dotcenter dotAg{sup +} becomes stabilized in hydrated zeolites and Ag{sub 6}{sup n+} in dehydrated ones. Silver hexamers have been reacted with various molecular adsorbates. The reaction rate depends on molecular size and nucleophilic character of adsorbate. In the presence of water and small alcohols silver hexamers are transformed to the elongated tetramers. (author).

  18. Catalytic Activity of Cationic and Neutral Silver(I)-XPhos Complexes with Nitrogen Ligands or Tolylsulfonate for Mannich and Aza-Diels-Alder Coupling Reactions.

    Science.gov (United States)

    Grirrane, Abdessamad; Álvarez, Eleuterio; García, Hermenegildo; Corma, Avelino

    2016-01-01

    Cationic and neutral silver(I)-L complexes (L=Buchwald-type biaryl phosphanes) with nitrogen co-ligands or organosulfonate counter ions have been synthesised and characterised through their structural and spectroscopic properties. At room temperature, both cationic and neutral silver(I)-L complexes are extremely active catalysts in the promotion of the single and double A(3) coupling of terminal (di)alkynes, pyrrolidine and formaldehyde. In addition, the aza-Diels-Alder two- and three-component coupling reactions of Danishefsky's diene with an imine or amine and aldehyde are efficiently catalysed by these cationic or neutral silver(I)-L complexes. The solvent influences the catalytic performance due to limited complex solubility or solvent decomposition and reactivity. The isolation of new silver(I)-L complexes with reagents as ligands lends support to mechanistic proposals for such catalytic processes. The activity, stability and metal-distal arene interaction of these silver(I)-L catalysts have been compared with those of analogous cationic gold(I) and copper(I) complexes. PMID:26598792

  19. Effect of particle clustering of silver nanoparticles on ultrathin silicon solar cell

    Science.gov (United States)

    Shokeen, Poonam; Jain, Amit; Kapoor, Avinashi; Gupta, Vinay

    2016-07-01

    Particle clustering is a major concern for uniform dispersal of nanoparticles in various deposition procedures. Well separated uniform distribution of metal nanoparticles is essential for effective coupling of surface plasmons. This work experimentally and theoretically, discusses the effect of nanoparticle clustering on the light trapping efficiency of silver nanoparticles. Pulsed laser deposition system has been used for deposition of silver nanoparticles, and substrate heating has been used to promote uniform distribution of nanoparticles. Pre-heated substrate depositions are compared with corresponding post-annealed samples. XRD, FESEM, Photoluminescence and UV-visible spectroscopy have been used to study the variations in their structural and optical properties. Mono-dispersal of silver nanoparticles for pre-heated substrates results in sharper surface plasmon resonance in comparison to post-annealed samples. Mie theory is used to estimate the particle size of the nanoparticles and findings are in accordance with quantitative analysis of FESEM images. Finite-difference time domain technique is used to discuss the effect of particle distribution on an ultrathin film silicon solar cell. Device degradation is observed as a result of clustering of silver nanoparticles. Hence, mono-dispersal of plasmonic nanostructures is important for required results and pre-heated deposition of metal nanoparticles by pulsed laser deposition can effectively solve the problem of particle clustering.

  20. Structural and electronic properties of small silver-sulfur clusters: A density functional study

    Science.gov (United States)

    Li, Yan-Fang; Li, Yang; Li, Ying; Tan, Jia-Jin; Li, Hui-Li

    2016-10-01

    Density functional theory calculations have been performed to systematically investigate the structural and electronic properties of neutral and anionic AgnSm (2≤n+m≤6) clusters. The results show that the ground-state structures of neutral clusters are different from those of anionic clusters. Theoretical electron detachment energies (both vertical and adiabatic) are compared with the experimental measurements to verify the ground states of silver-sulfur clusters obtained in the present study. For both neutral and anionic systems, the highest occupied-lowest unoccupied molecular orbital energy gaps exhibit an odd-even oscillation as a function of the cluster size. In addition, the natural population analysis reveals that the charges transfer from Ag atoms to S atoms in AgnSm clusters, and the extra electron of AgnSm- clusters is mainly localized on the 3p subshells of S atoms.

  1. Enantiopure Radical Cation Salt Based on Tetramethyl-Bis(ethylenedithio-Tetrathiafulvalene and Hexanuclear Rhenium Cluster

    Directory of Open Access Journals (Sweden)

    Flavia Pop

    2016-01-01

    Full Text Available Electrocrystallization of the (S,S,S,S enantiomer of tetramethyl-bis(ethylenedithio-tetrathiafulvalene donor 1 in the presence of the dianionic hexanuclear rhenium (III cluster [Re6S6Cl8]2− affords a crystalline radical cation salt formulated as [(S-1]2·Re6S6Cl8, in which the methyl substituents of the donors adopt an unprecedented all-axial conformation. A complex set of intermolecular TTF···TTF and cluster···TTF interactions sustain an original tridimensional architecture.

  2. Revisiting benzene cluster cations for the chemical ionization of dimethyl sulfide and select volatile organic compounds

    Science.gov (United States)

    Kim, Michelle J.; Zoerb, Matthew C.; Campbell, Nicole R.; Zimmermann, Kathryn J.; Blomquist, Byron W.; Huebert, Barry J.; Bertram, Timothy H.

    2016-04-01

    Benzene cluster cations were revisited as a sensitive and selective reagent ion for the chemical ionization of dimethyl sulfide (DMS) and a select group of volatile organic compounds (VOCs). Laboratory characterization was performed using both a new set of compounds (i.e., DMS, β-caryophyllene) as well as previously studied VOCs (i.e., isoprene, α-pinene). Using a field deployable chemical-ionization time-of-flight mass spectrometer (CI-ToFMS), benzene cluster cations demonstrated high sensitivity (> 1 ncps ppt-1) to DMS, isoprene, and α-pinene standards. Parallel measurements conducted using a chemical-ionization quadrupole mass spectrometer, with a much weaker electric field, demonstrated that ion-molecule reactions likely proceed through a combination of ligand-switching and direct charge transfer mechanisms. Laboratory tests suggest that benzene cluster cations may be suitable for the selective ionization of sesquiterpenes, where minimal fragmentation (validated against an atmospheric pressure ionization mass spectrometer, where measurements from the two instruments were highly correlated (R2 > 0.95, 10 s averages) over a wide range of sampling conditions.

  3. Acid decomposition and thiourea leaching of silver from hazardous jarosite residues: Effect of some cations on the stability of the thiourea system.

    Science.gov (United States)

    Calla-Choque, D; Nava-Alonso, F; Fuentes-Aceituno, J C

    2016-11-01

    The recovery of silver from hazardous jarosite residues was studied employing thiourea as leaching agent at acid pH and 90°C. The stability of the thiourea in synthetic solutions was evaluated in the presence of some cations that can be present in this leaching system: cupric and ferric ions as oxidant species, and zinc, lead and iron as divalent ions. Two silver leaching methods were studied: the simultaneous jarosite decomposition-silver leaching, and the jarosite decomposition followed by the silver leaching. The study with synthetic solutions demonstrated that cupric and ferric ions have a negative effect on thiourea stability due to their oxidant properties. The effect of cupric ions is more significant than the effect of ferric ions; other studied cations (Fe(2+), Zn(2+), Pb(2+)) had no effect on the stability of thiourea. When the decomposition of jarosite and the silver leaching are carried out simultaneously, 70% of the silver can be recovered. When the acid decomposition was performed at pH 0.5 followed by the leaching step at pH 1, total silver recovery increased up to 90%. The zinc is completely dissolved with any of these processes while the lead is practically insoluble with these systems producing a lead-rich residue. PMID:27322901

  4. Infrared Photodissociation Spectra of Mass-Selected Homoleptic Dinuclear Palladium Carbonyl Cluster Cations in the Gas Phase

    Institute of Scientific and Technical Information of China (English)

    崔洁铭; 邢小鹏; 池超贤; 王冠军; 刘智攀; 周鸣飞

    2012-01-01

    Infrared spectra of mass-selected homoleptic dinuclear palladium carbonyl cluster cations Pd2(CO)n (n=5 8) are measured via infrared photodissociation spectroscopy in the carbonyl stretching frequency region. The structures are established by comparison of the experimental spectra with simulated spectra derived from density functional calculations. The Pd2(CO)+ cation is characterized to have two weakly semibridging CO groups with C2 symmetry. The Pd2(CO)6+ and Pd2(CO)7+ cations are determined to involve one weakly semibridging CO group. The Pd2(CO)8+ cation is a CO coordination saturated cluster, which is determined to have a D2d structure with all of the carbonyl groups terminally bonded. Bonding analysis indicates that these cluster cations each has a Pd--Pd half bond. The Pd--Pd distance increases with the number of CO ligands.

  5. Formation of binary silver sulfide clusters and sulfur sensitization of photographic process

    Institute of Scientific and Technical Information of China (English)

    彭必先; 崔卫东; 于忠德; 高振; 朱起鹤; 孔繁敖

    1997-01-01

    Formation of silver sulfide binary cluster ions,as well as the effects of silver and sulfur content proportion,the cluster size range,the influence of laser fluence,the UV laser photolysis,etc.,was studied with the laser ablation method and a tandem time-of-flight mass spectrometer.The results show that there exist two different forms of positively charge-bearing cluster ions;[(Ag2S)n Ag] + and [ (Ag2S)n-1 Ag3]+.The most possible forms of the sulfur sensitization centers acting as traps of photoelectrons are [Ag2S] +,[ Ag2S Ag] +,[ Ag2S Ag3]+ and the analogs.

  6. Long-lived charge-separated states in ligand-stabilized silver clusters

    KAUST Repository

    Pelton, Matthew

    2012-07-25

    Recently developed synthesis methods allow for the production of atomically monodisperse clusters of silver atoms stabilized in solution by aromatic thiol ligands, which exhibit intense absorption peaks throughout the visible and near-IR spectral regions. Here we investigated the time-dependent optical properties of these clusters. We observed two kinetic processes following ultrafast laser excitation of any of the absorption peaks: a rapid decay, with a time constant of 1 ps or less, and a slow decay, with a time constant that can be longer than 300 ns. Both time constants decrease as the polarity of the solvent increases, indicating that the two processes correspond to the formation and recombination, respectively, of a charge-separated state. The long lifetime of this state and the broad optical absorption spectrum mean that the ligand-stabilized silver clusters are promising materials for solar energy harvesting. © 2012 American Chemical Society.

  7. Cluster-Continuum Calculations of Hydration Free Energies of Anions and Group 12 Divalent Cations

    Energy Technology Data Exchange (ETDEWEB)

    Guo, Hao-Bo [ORNL; Liang, Liyuan [ORNL; Parks, Jerry M [ORNL; Smith, Jeremy C [ORNL; Riccardi, Demian M [ORNL; Gu, Baohua [ORNL

    2013-01-01

    Understanding aqueous phase processes involving group 12 metal cations is relevant to both environmental and biological sciences. Here, quantum chemical methods and polarizable continuum models are used to compute the hydration free energies of a series of divalent group 12 metal cations (Zn2+, Cd2+, and Hg2+) together with Cu2+ and the anions OH , SH , Cl , and F . A cluster-continuum method is employed, in which gas-phase clusters of the ion and explicit solvent molecules are immersed in a dielectric continuum. Two approaches to define the size of the solute-water cluster are compared, in which the number of explicit waters used is either held constant or determined variationally as that of the most favorable hydration free energy. Results obtained with various polarizable continuum models are also presented. Each leg of the relevant thermodynamic cycle is analyzed in detail to determine how different contributions yield the observed mean signed error (MSE) and the standard deviation of the error (STDEV) between theory and experiment. The use of a constant number of water molecules for each set of ions is found to lead to predicted relative trends that benefit from error cancellation. Overall, the best results are obtained with MP2 and the Solvent Model D polarizable continuum model (SMD), with eight explicit water molecules for anions and ten for the metal cations, yielding a STDEV of 2.3 kcal/mol and MSE of 0.9 kcal/mol between theoretical to experimental hydration free energies, which range from -72.4 kcal/mol for SH to -505.9 kcal/mol for Cu2+. Using B3PW91 with DFT-D3 dispersion corrections (B3PW91-D) and SMD yields a STDEV of 3.3 kcal mol 1 and MSE of 1.6 kcal/mol, to which adding MP2 corrections from smaller divalent metal ion water molecule clusters yields very good agreement with the full MP2 results. Using B3PW91-D and SMD, with two explicit water molecules for anions and six for divalent metal cations also yields reasonable agreement with experiment

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

    Science.gov (United States)

    Ono, Yoshio; Baba, Toshihide

    2015-06-28

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

  9. High reactivity of nanosized niobium oxide cluster cations in methane activation: A comparison with vanadium oxides.

    Science.gov (United States)

    Ding, Xun-Lei; Wang, Dan; Wu, Xiao-Nan; Li, Zi-Yu; Zhao, Yan-Xia; He, Sheng-Gui

    2015-09-28

    The reactions between methane and niobium oxide cluster cations were studied and compared to those employing vanadium oxides. Hydrogen atom abstraction (HAA) reactions were identified over stoichiometric (Nb2O5)N(+) clusters for N as large as 14 with a time-of-flight mass spectrometer. The reactivity of (Nb2O5)N(+) clusters decreases as the N increases, and it is higher than that of (V 2O5)N(+) for N ≥ 4. Theoretical studies were conducted on (Nb2O5)N(+) (N = 2-6) by density functional calculations. HAA reactions on these clusters are all favorable thermodynamically and kinetically. The difference of the reactivity with respect to the cluster size and metal type (Nb vs V) was attributed to thermodynamics, kinetics, the electron capture ability, and the distribution of the unpaired spin density. Nanosized Nb oxide clusters show higher HAA reactivity than V oxides, indicating that niobia may serve as promising catalysts for practical methane conversion. PMID:26429016

  10. MODIFICATION OF TRANSITION METAL CATIONS TO POLYMER- STABILIZED PLATINUM COLLOIDAL CLUSTERS IN ENANTIOSELECTIVE HYDROGENATION OF METHYL PYRUVATE

    Institute of Scientific and Technical Information of China (English)

    Xiao-ping Yan; Bao-lin He; Jie Zhang; Han-fan Liu

    2005-01-01

    Modification of transition metal cations to polymer-stabilized Pt colloidal clusters modified with cinchonidine was studied in enantioselective hydrogenation of methyl pyruvate. Compared to the enantiomeric excess (e.e.) value (71.4%)obtained without the presence of metal cations, obvious e.e. enhancement (up to 82.5%) was resulted from the addition of Zn2+ but with a certain decrease in activity. The reaction parameters in the presence of Zn2+ were also studied. It was found that the Pt colloidal catalysts in the presence of metal cations performed very differently from that in the absence of metal cations.

  11. Charge-transfer interactions between TCNQ and silver clusters Ag20 and Ag13.

    Science.gov (United States)

    Chen, Jing; Zhang, Hanyu; Liu, Xianhu; Yuan, Chengqian; Jia, Meiye; Luo, Zhixun; Yao, Jiannian

    2016-03-14

    Interactions between tetracyanoquinodimethane (TCNQ) and two typical silver clusters Ag13 and Ag20 are studied by first-principles DFT calculations. Charge transfer (CT) from silver clusters to TCNQ molecules initiates the Ag-N bond formation at selective sites resulting in the formation of different isomers of Ag13-TCNQ and Ag20-TCNQ complexes. We show here a comprehensive spectroscopic analysis for the two CT complexes on the basis of Raman and infrared activities. Furthermore, frontier molecular orbital (FMO) and natural bond orbital (NBO) analysis of the complexes provides a vivid illustration of electron cloud overlap and interactions. The behavior of TCNQ adsorbed on the tetrahedral Ag20 cluster was even found in good agreement with the experimental measurement of TCNQ molecules on a single-crystal Ag(111) surface. This study not only endeavors to clarify the charge-transfer interactions of TCNQ with silver, but also presents a finding of enhanced charge transfer between Ag13 and TCNQ indicating potential for candidate building blocks of granular materials. PMID:26888771

  12. Synthesis, characterization and optical properties of low nuclearity liganded silver clusters: Ag31(SG)19 and Ag15(SG)11

    Science.gov (United States)

    Bertorelle, Franck; Hamouda, Ramzi; Rayane, Driss; Broyer, Michel; Antoine, Rodolphe; Dugourd, Philippe; Gell, Lars; Kulesza, Alexander; MitrićPresent Address: Institut Für Physikalische Und Theoretische Chemie, Julius-Maximilians Universität Würzburg, Emil-Fischer-Straße 42, 97074 Würzburg, Germany, Roland; Bonačić-Koutecký, Vlasta

    2013-05-01

    We report a simple synthesis of silver:glutathione (Ag:SG) clusters using a cyclic reduction under oxidative conditions. Two syntheses are described which lead to solutions containing well-defined Ag31(SG)19 and Ag15(SG)11 clusters that have been characterized by mass spectrometry. The optical properties of silver:glutathione (Ag:SG) cluster solutions have been investigated experimentally. In particular, the solution containing Ag15(SG)11 clusters shows a bright and photostable emission. For Ag31(SG)19 and Ag15(SG)11 clusters, the comparison of experimental findings with DFT and TDDFT calculations allowed us to reveal the structural and electronic properties of such low nuclearity liganded silver clusters.We report a simple synthesis of silver:glutathione (Ag:SG) clusters using a cyclic reduction under oxidative conditions. Two syntheses are described which lead to solutions containing well-defined Ag31(SG)19 and Ag15(SG)11 clusters that have been characterized by mass spectrometry. The optical properties of silver:glutathione (Ag:SG) cluster solutions have been investigated experimentally. In particular, the solution containing Ag15(SG)11 clusters shows a bright and photostable emission. For Ag31(SG)19 and Ag15(SG)11 clusters, the comparison of experimental findings with DFT and TDDFT calculations allowed us to reveal the structural and electronic properties of such low nuclearity liganded silver clusters. Electronic supplementary information (ESI) available: Optimal settings for the MS instrument; schematic diagrams for syntheses A and B; ESI mass spectra of silver clusters from ``synthesis A'' in different solvent mixtures, at different pH values and with different synthesis protocols; excitation and emission spectra of clusters from ``synthesis B'' in water and of the separated band after PAGE separation; lifetime measurements of silver clusters from a solution of ``synthesis B'' in water; the structure and absorption spectrum of the two lowest-energy isomers

  13. Experimental and theoretical study on interaction of the silver cation with nonactin

    Science.gov (United States)

    Makrlík, Emanuel; Vaňura, Petr

    2015-12-01

    From extraction experiments and γ-activity measurements, the extraction constant corresponding to the equilibrium ? occurring in the two-phase water-nitrobenzene system (1 = nonactin, aq = aqueous phase, nb = nitrobenzene phase) was evaluated as log Kex (Ag+, 1 ṡ Na+) = 0.6 ± 0.1. Furthermore, the stability constant of the 1 ṡ Ag+ complex in nitrobenzene saturated with water was calculated for a temperature of 25 °C: log βnb(1 ṡ Ag+) = 6.6 ± 0.2. Finally, employing quantum mechanical calculations, the most probable structure of the cationic complex species 1 ṡ Ag+ was derived. In the resulting complex, having a tennis-ball-seam conformation with the C2 symmetry, the 'central' cation Ag+ is bound by eight relatively strong bonding interactions to eight oxygen atoms of the parent nonactin ligand. The interaction energy of the considered 1 ṡ Ag+ complex was found to be -468.5 kJ/mol, confirming also the formation of this cationic species.

  14. Radiation-induced silver agglomeration in molecular sieves: a comparison between A and X zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Sadlo, J.; Wasowicz, T.; Michalik, J. [Institute of Nuclear Chemistry and Technology, Warsaw (Poland)

    1995-06-01

    The stabilization conditions of silver atoms and clusters in hydrated and dehydrated AgNa-A and AgNa-X zeolites {gamma}-irradiated at 77 K have been studied by ESR. It was found that silver agglomeration mechanisms in hydrated A and X zeolites are very similar and are controlled by the migration of silver atoms into the {alpha}-cages. In dehydrated zeolites agglomeration leads to completely different silver clusters in A and X zeolites. Small cationic clusters are stabilized in A zeolites and metallic clusters in X zeolites. Various factors affecting the agglomeration process in A and X zeolites are discussed. (author).

  15. Vibrational anharmonicity of small gold and silver clusters using the VSCF method.

    Science.gov (United States)

    Mancera, Luis A; Benoit, David M

    2016-01-01

    We study the vibrational spectra of small neutral gold (Au2-Au10) and silver (Ag2-Au5) clusters using the vibrational self-consistent field method (VSCF) in order to account for anharmonicity. We report harmonic, VSCF, and correlation-corrected VSCF calculations obtained using a vibrational configuration interaction approach (VSCF/VCI). Our implementation of the method is based on an efficient calculation of the potential energy surfaces (PES), using periodic density functional theory (DFT) with a plane-wave pseudopotential basis. In some cases, we use an efficient technique (fast-VSCF) assisted by the Voter-Chen potential in order to get an efficient reduction of the number of pair-couplings between modes. This allows us to efficiently reduce the computing time of 2D-PES without degrading the accuracy. We found that anharmonicity of the gold clusters is very small with maximum rms deviations of about 1 cm(-1), although for some particular modes anharmonicity reaches values slightly larger than 2 cm(-1). Silver clusters show slightly larger anharmonicity. In both cases, large differences between calculated and experimental vibrational frequencies (when available) stem more likely from the quality of the electronic structure method used than from vibrational anharmonicity. We show that noble gas embedding often affects the vibrational properties of these clusters more than anharmonicity, and discuss our results in the context of experimental studies. PMID:26619274

  16. Structure and annealing of cation Frenkel defects in silver halides after irradiation with thermal neutrons

    International Nuclear Information System (INIS)

    Polarised 110Ag(I=1,Tsub(1/2)=24.6s) nuclei were produced in the reaction 109Ag(nsub(pol),γ)110Ag in AgCl and AgBr single crystals. The hyperfine interaction of the 110Ag nuclei with radiation-induced point defects has been studied. Positions and shapes of nuclear magnetic resonance curves could be explained assuming a random distribution of positively and negatively charged point defects. From this analysis and from additionally measured migration enthalpies, derived from annealing stages, the defects could be identified as cation Frenkel pairs. The nuclear quadrupole moment of 110Ag was determined as Q=0.24x10-24cm2 by measuring the spin-lattice relaxation time of the 110Ag nuclei. (author)

  17. Experimental and theoretical studies of the reaction between cationic vanadium oxide clusters and acetylene

    Institute of Scientific and Technical Information of China (English)

    YIN Shi; MA YanPing; DU Lin; HE ShengGui; GE MaoFa

    2008-01-01

    The time of flight mass spectrometer coupled with a laser ablation/supersonic expansion cluster source and a fast flow reactor was adopted to study the reactivity of cationic vanadium oxide clusters (VmO+n) toward acetylene (C2H2) molecules under gas phase (P, ~ 1.14 kPa), under near room temperature (T, ~ 350 K) conditions. Association products, VmOnC2H+2 (m,n = 2,4; 2,6; 3,7-8; 4,9-11; 5,12-13;6,13-16, and 7,17), are observed. The oxidation of C2H2 by (V2O5)+n, (n = 1-3) is experimentally identified.The reactivity of (V2O5)+n decreases as n increases. Density functional theory (DFT) calculations were carried out to interpret the reaction mechanisms. The DFT results indicate that a terminal oxygen atom from V2O+5 can transfer overall barrierlessly to C2H2 at room temperature, which is in agreement with the experimental observation. Other experimental results such as the observation of V2O6C2H+2 and nonobservation of V2O7,8C2H+2 in the experiments are also well interpreted based on the DFT calculations.The reactivity of vanadium oxide clusters toward acetylene and other hydrocarbons may be considered in identifying molecular level mechanisms for related heterogeneous catalysis.

  18. Theoretical study of partial oxidation of ethylene by vanadium trioxide cluster cation

    Institute of Scientific and Technical Information of China (English)

    WANG ZheChen; DING XunLei; MA YanPing; CAO Hai; WU XiaoNan; ZHAO YanXia; HE ShengGui

    2009-01-01

    Density functional theory (DFT) study of reaction between vanadium trioxide cluster cation (VO+3) and ethylene (C2H4) to yield VO+2 + CH3CHO (acetaldehyde) and VO2CH+2 + HCHO (formaldehyde) is carried out.Structures of all reactants,products,intermediates,and transition state in the reaction have been optimized and characterized.The results show unexpected barriers in the reaction due to the existence of a η2-O2 moiety in the ground state structure of VO+3.The initial reaction steps combining ethylene adsorption,C=C activation and O-O cleavage are proposed as rate limiting processes.Comparison of reactions of VO+3 + C2H4 with VO3 + C2H4 and VO+2 + C2H4 in the previous studies is made in detail.The results of this work may shed light on the understanding of C=C bond cleavage in related heterogeneous catalysis.

  19. First principle study of the interaction of elemental Hg with small neutral, anionic and cationic Pd ( = 1-6) clusters

    Indian Academy of Sciences (India)

    Shamoon Ahmad Siddiqui; Nadir Bouarissa

    2013-11-01

    Density functional theory (DFT)-based calculations have been performed so as to study the interaction of elemental mercury (Hg) with small neutral, cationic and anionic palladium clusters (Pd, = 1-6). Results of these calculations clearly indicate that frontier molecular orbital (FMO) theory is a useful method to predict the selectivity of Hg adsorption. Binding energies of Hg on cationic Pd clusters are generally found to be greater than those on neutral and anionic clusters. Results of natural bond orbital (NBO) analysis show that the flow of electrons in the neutral and charged complexes is mainly due to s orbitals of Hg. NBO analysis also indicates that, in most of the cases, the binding energies of Hg with Pdn clusters are directly proportional to charge transfer, i.e., greater the charge transfer, higher is the binding energy.

  20. Dimensional scale effects on surface enhanced Raman scattering efficiency of self-assembled silver nanoparticle clusters

    International Nuclear Information System (INIS)

    A study of the Surface Enhanced Raman Scattering (SERS) from micrometric metallic nanoparticle aggregates is presented. The sample is obtained from the self-assembly on glass slides of micro-clusters of silver nanoparticles (60 and 100 nm diameter), functionalized with the organic molecule 4-aminothiophenol in water solution. For nanoparticle clusters at the micron scale, a maximum enhancement factor of 109 is estimated from the SERS over the Raman intensity ratio normalized to the single molecule contribution. Atomic force microscopy, correlated to spatially resolved Raman measurements, allows highlighting the connection between morphology and efficiency of the plasmonic system. The correlation between geometric features and SERS response of the metallic structures reveals a linear trend of the cluster maximum scattered intensity as a function of the surface area of the aggregate. On given clusters, the intensity turns out to be also influenced by the number of stacking planes of the aggregate, thus suggesting a plasmonic waveguide effect. The linear dependence results weakened for the largest area clusters, suggesting 30 μm2 as the upper limit for exploiting the coherence over large scale of the plasmonic response.

  1. Dimensional scale effects on surface enhanced Raman scattering efficiency of self-assembled silver nanoparticle clusters

    Energy Technology Data Exchange (ETDEWEB)

    Fasolato, C. [Dip. Fisica, Università Sapienza, P.le Aldo Moro, 5, 00185 Rome (Italy); Center for Life Nanoscience@Sapienza, Istituto Italiano di Tecnologia, V.le Regina Elena, 291, 00185 Rome (Italy); Domenici, F., E-mail: fabiodomenici@gmail.com, E-mail: paolo.postorino@roma1.infn.it; De Angelis, L.; Luongo, F.; Postorino, P., E-mail: fabiodomenici@gmail.com, E-mail: paolo.postorino@roma1.infn.it [Dip. Fisica, Università Sapienza, P.le Aldo Moro, 5, 00185 Rome (Italy); Sennato, S. [Dip. Fisica, Università Sapienza, P.le Aldo Moro, 5, 00185 Rome (Italy); CNR-IPCS UOS Roma, Dip. Fisica, Università Sapienza, P.le Aldo Moro, 5, 00185 Rome (Italy); Mura, F. [Dip. Scienze di Base Applicate all' Ingegneria, Università Sapienza, Via A. Scarpa, 16, 00185 Rome (Italy); Costantini, F. [Dip. Ingegneria Astronautica Elettrica ed Energetica, Università Sapienza, Via Eudossiana, 18, 00184 Rome (Italy); Bordi, F. [Dip. Fisica, Università Sapienza, P.le Aldo Moro, 5, 00185 Rome (Italy); Center for Life Nanoscience@Sapienza, Istituto Italiano di Tecnologia, V.le Regina Elena, 291, 00185 Rome (Italy); CNR-IPCS UOS Roma, Dip. Fisica, Università Sapienza, P.le Aldo Moro, 5, 00185 Rome (Italy)

    2014-08-18

    A study of the Surface Enhanced Raman Scattering (SERS) from micrometric metallic nanoparticle aggregates is presented. The sample is obtained from the self-assembly on glass slides of micro-clusters of silver nanoparticles (60 and 100 nm diameter), functionalized with the organic molecule 4-aminothiophenol in water solution. For nanoparticle clusters at the micron scale, a maximum enhancement factor of 10{sup 9} is estimated from the SERS over the Raman intensity ratio normalized to the single molecule contribution. Atomic force microscopy, correlated to spatially resolved Raman measurements, allows highlighting the connection between morphology and efficiency of the plasmonic system. The correlation between geometric features and SERS response of the metallic structures reveals a linear trend of the cluster maximum scattered intensity as a function of the surface area of the aggregate. On given clusters, the intensity turns out to be also influenced by the number of stacking planes of the aggregate, thus suggesting a plasmonic waveguide effect. The linear dependence results weakened for the largest area clusters, suggesting 30 μm{sup 2} as the upper limit for exploiting the coherence over large scale of the plasmonic response.

  2. Ag44(SeR)30: A Hollow Cage Silver Cluster with Selenolate Protection.

    Science.gov (United States)

    Chakraborty, Indranath; Kurashige, Wataru; Kanehira, Keita; Gell, Lars; Häkkinen, Hannu; Negishi, Yuichi; Pradeep, Thalappil

    2013-10-01

    Selenolate protected, stable and atomically precise, hollow silver cluster was synthesized using solid state as well as solution state routes. The optical absorption spectrum shows multiple and sharp features similar to the thiolated Ag44 cluster, Ag44(SR)30 whose experimental structure was reported recently. High-resolution electrospray ionization mass spectrometry (HRESI MS) shows well-defined molecular ion features with two, three, and four ions with isotopic resolution, due to Ag44(SePh)30. Additional characterization with diverse tools confirmed the composition. The closed-shell 18 electron superatom electronic structure, analogous to Ag44(SR)30 stabilizes the dodecahedral cage with a large HOMO-LUMO gap of 0.71 eV. The time-dependent density functional theory (TDDFT) prediction of the optical absorption spectrum, assuming the Ag44(SR)30 structure, matches the experimental data, confirming the structure.

  3. One-dimensional polymers based on silver(I) cations and organometallic cyclo-P3 ligand complexes.

    Science.gov (United States)

    Gregoriades, Laurence J; Wegley, Brian K; Sierka, Marek; Brunner, Eike; Gröger, Christian; Peresypkina, Eugenia V; Virovets, Alexander V; Zabel, Manfred; Scheer, Manfred

    2009-10-01

    The synthesis and characterization of the first supramolecular aggregates incorporating the organometallic cyclo-P3 ligand complexes [CpRMo(CO)2(eta3-P3)] (CpR=Cp (C5H5; 1a), Cp* (C5(CH3)5; 1b)) as linking units is described. The reaction of the Cp derivative 1a with AgX (X=CF3SO3, Al{OC(CF3)3}4) yields the one-dimensional (1D) coordination polymers [Ag{CpMo(CO)2(mu,eta3:eta1:eta1-P3)}2]n[Al{OC(CF3)3}4]n (2) and [Ag{CpMo(CO)2(mu,eta3:eta1:eta1-P3)}3]n[X]n (X=CF3SO3 (3a), Al{OC(CF3)3}4 (3b)). The solid-state structures of these polymers were revealed by X-ray crystallography and shown to comprise polycationic chains well-separated from the weakly coordinating anions. If AgCF3SO3 is used, polymer 3a is obtained regardless of reactant stoichiometry whereas in the case of Ag[Al{OC(CF3)3}4], reactant stoichiometry plays a decisive role in determining the structure and composition of the resulting product. Moreover, polymers 3a, b are the first examples of homoleptic silver complexes in which Ag(I) centers are found octahedrally coordinated to six phosphorus atoms. The Cp* derivative 1b reacts with Ag[Al{OC(CF3)3}4] to yield the 1D polymer [Ag{Cp*Mo(CO)2(mu,eta3:eta2:eta1-P3)}2]n[Al{OC(CF3)3}4]n (4), the crystal structure of which differs from that of polymer 2 in the coordination mode of the cyclo-P3 ligands: in 2, the Ag+ cations are bridged by the cyclo-P3 ligands in a eta1:eta1 (edge bridging) fashion whereas in 4, they are bridged exclusively in a eta2:eta1 mode (face bridging). Thus, one third of the phosphorus atoms in 2 are not coordinated to silver while in 4, all phosphorus atoms are engaged in coordination with silver. Comprehensive spectroscopic and analytical measurements revealed that the polymers 2, 3a, b, and 4 depolymerize extensively upon dissolution and display dynamic behavior in solution, as evidenced in particular by variable temperature 31P NMR spectroscopy. Solid-state 31P magic angle spinning (MAS) NMR measurements, performed on the polymers 2, 3

  4. Nitrogen Molecule Adsorption on Cationic Tantalum Clusters and Rhodium Clusters and Desorption from Their Nitride Clusters Studied by Thermal Desorption Spectrometry.

    Science.gov (United States)

    Mafuné, Fumitaka; Tawaraya, Yuki; Kudoh, Satoshi

    2016-06-23

    Adsorption and desorption of N2 molecules onto cationic Ta and Rh clusters in the gas phase were investigated in the temperature range of 300-1000 K by using thermal desorption spectrometry in combination with density functional theory (DFT) calculations. For Ta6(+), the first N2 molecule was found to adsorb dissociatively, and it remained adsorbed when Ta6(+)N2 was heated to 1000 K. In contrast, the second and the subsequent N2 molecules adsorbed weakly as a molecular form and were released into the gas phase when heated to 600 K. The difference can be explained in terms of the activation barrier between the molecular and dissociative forms. On the other hand, when Ta clusters were generated in the presence of N2 gas by the laser ablation of a Ta rod, isomeric clusters, TanNm(+), having heat resistivity were formed. For Rh6(+), N2 adsorbed molecularly at 300 K and desorbed totally at 450 K. These results were consistent with the DFT calculations, indicating that the dissociative adsorption of N2 is endothermic. PMID:27276438

  5. Cation-interlinking network cluster approach in application to extended defects in covalent-bonded glassy semiconductors

    Energy Technology Data Exchange (ETDEWEB)

    Shpotyuk, Oleh [Lviv Institute of Materials of SRC, Lviv (Ukraine); Institute of Physics, Jan Dlugosz University, Czestochowa (Poland); Boyko, Vitaliy [Lviv Institute of Materials of SRC, Lviv (Ukraine); Lviv Polytechnic National University (Ukraine); Hyla, Malgorzata [Institute of Physics, Jan Dlugosz University, Czestochowa (Poland)

    2009-08-15

    A principally new cation-interlinking network cluster approach (CINCA) was proposed to describe different types of glass-forming structural units in network covalent-bonded solids like to chalcogenide vitreous semiconductors. Within this approach, two (or three) interconnected cation-centered polyhedra form more stretched structural fragments conditionally named atomic clusters, reflecting in such a way whole backbone of covalent-bonded semiconductor multiply duplicated in a space. The probability of possible atomic clusters is estimated with numerical parameter giving average formation energy in respect to the number of atoms involved in the cluster and average coordination number. This approach was probed at the example of regular network clusters based on AsS{sub 3/2} pyramids mutually-interconnected through bridge -S- atom contrasted with irregular double-bond-based quasi-tetrahedral structural S=AsS{sub 3} defects within binary As-S system. The corresponding mathematical calculations confirming a preference of regularly-linked structural units over irregular ones was performed using HyperChem 7.5 program. (copyright 2009 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  6. Near infrared emission from molecule-like silver clusters confined in zeolite A assisted by thermal activation

    Energy Technology Data Exchange (ETDEWEB)

    Lin, Hui, E-mail: linh8112@163.com; Imakita, Kenji; Rong Gui, Sa Chu; Fujii, Minoru, E-mail: fujii@eedept.kobe-u.ac.jp [Department of Electrical and Electronic Engineering, Graduate School of Engineering, Kobe University, Rokkodai, Nada, Kobe 657-8501 (Japan)

    2014-07-07

    Strong and broad near infrared (NIR) emission peaked at ~855 nm upon optimal excitation at 342 nm has been observed from molecule-like silver clusters (MLSCs) confined in zeolite A assisted by thermal activation. To the best of our knowledge, this is the first observation of NIR emission peaked at longer than 800 nm from MLSCs confined in solid matrices. The decay time of the NIR emission is over 10 μs, which indicates that it is a spin-forbidden transition. The ~855 nm NIR emission shows strong dependence on the silver loading concentration and the thermal activation temperature.

  7. The effect of counteranions on the molecular structures of phosphanegold(i) cluster cations formed by polyoxometalate (POM)-mediated clusterization.

    Science.gov (United States)

    Nagashima, Eri; Yoshida, Takuya; Matsunaga, Satoshi; Nomiya, Kenji

    2016-09-14

    The effect of counteranions on the molecular structures of phosphanegold(i) cluster cations formed by polyoxometalate (POM)-mediated clusterization was investigated. A novel intercluster compound, [{(AuLCl)2(μ-OH)}2]3[α-PMo12O40]2·3EtOH (1-PMo12), was obtained as orange-yellow plate crystals in 12.0% yield from a 6 : 1 molar ratio reaction of the monomeric phosphanegold(i) carboxylato complex [Au(RS-pyrrld)(LCl)] (RS-Hpyrrld = RS-2-pyrrolidone-5-carboxylic acid; LCl = tris(4-chlorophenyl)phosphane) in CH2Cl2 with the free acid-form of Keggin polyoxometalate (POM), H3[α-PMo12O40]·14H2O. An EtOH/H2O (5 : 1, v/v) solvent mixture was used. The dimeric cation [{(AuLCl)2(μ-OH)}2](2+) in 1-PMo12 was in a parallel-edge arrangement that was formed by self-assembly through the inter-cationic aurophilic interactions of the μ-OH-bridged dinuclear phosphanegold(i) cation. The POM anion in 1-PMo12 was successfully exchanged with a smaller PF6(-) anion by the use of an anion-exchange resin. POM-free, colorless block crystals of [{(AuLCl)3(μ3-O)}2](PF6)2·4CH2Cl2 (2-PF6) were obtained by vapor diffusion in 14.1% yield. During the synthesis of 2-PF6, a compound with mixed counteranions (one POM and one PF6(-) anion), i.e. [{(AuLCl)4(μ4-O)}]2[α-PMo12O40]PF6 (3-PMo12PF6), was obtained in 66.4% yield. Both products were characterized by elemental analysis, TG/DTA, FT-IR, (31)P{(1)H} NMR, (1)H NMR, and X-ray crystallography. X-ray crystallography revealed that the countercation in 2-PF6 was the dimeric cation of the μ3-O-bridged tris{phosphanegold(i)} species, whereas that in 3-PMo12PF6 consisted of an unusual μ4-O-bridged tetragonal-pyramidal tetrakis{phosphanegold(i)} cation. Therefore, we concluded that the POM anion significantly contributed to the stabilization of these countercations (parallel-edged arrangement in 1-PMo12 and μ4-O-bridged tetragonal-pyramid in 3-PMo12PF6). Moreover, the previously reported yellow crystals of [{(AuLF)2(μ-OH)}2]3[PMo12O40]2·3

  8. Stable compositions and geometrical structures of titanium oxide cluster cations and anions studied by ion mobility mass spectrometry

    Science.gov (United States)

    Ohshimo, Keijiro; Norimasa, Naoya; Moriyama, Ryoichi; Misaizu, Fuminori

    2016-05-01

    Geometrical structures of titanium oxide cluster cations and anions have been investigated by ion mobility mass spectrometry and quantum chemical calculations based on density functional theory. Stable cluster compositions with respect to collision induced dissociation were also determined by changing ion injection energy to an ion drift cell for mobility measurements. The TinO2n-1+ cations and TinO2n- anions were predominantly observed at high injection energies, in addition to TinO2n+ for cations and TinO2n+1- for anions. Collision cross sections of TinO2n+ and TinO2n+1- for n = 1-7, determined by ion mobility mass spectrometry, were compared with those obtained theoretically as orientation-averaged cross sections for the optimized structures by quantum chemical calculations. All of the geometrical structures thus assigned have three-dimensional structures, which are in marked contrast with other oxides of late transition metals. One-oxygen atom dissociation processes from TinO2n+ and TinO2n+1- by collisions were also explained by analysis of spin density distributions.

  9. General Assembly of Twisted Trigonal-Prismatic Nonanuclear Silver(I) Clusters.

    Science.gov (United States)

    Li, Xiao-Yu; Su, Hai-Feng; Zhou, Rui-Qi; Feng, Sheng; Tan, Yuan-Zhi; Wang, Xing-Po; Jia, Jiong; Kurmoo, Mohamedally; Sun, Di; Zheng, Lan-Sun

    2016-02-24

    A general class of C3 -symmetric Ag9 clusters, [Ag9 S(tBuC6 H4 S)6 (dpph)3 (CF3 SO3 )] (1), [Ag9 (tBuC6 H4 S)6 (dpph)3 (CF3 SO3 )2 ]⋅CF3 SO3 (2), [Ag9 (tBuC6 H4 S)6 (dpph)3 (NO3 )2 ] ⋅NO3 (3), and [Ag9 (tBuC6 H4 S)7 (dpph)3 (Mo2 O7 )0.5 ]2 ⋅2 CF3 COO (4) (dpph=1,6-bis(diphenylphosphino)hexane), with a twisted trigonal-prism geometry was isolated by the reaction of polymeric {(HNEt3 )2 [Ag10 (tBuC6 H4 S)12 ]}n , 1,6-bis(diphenylphosphino)hexane, and various silver salts under solvothermal conditions. The structures consist of discrete clusters constructed from a girdling Ag9 twisted trigonal prism with the top and bottom trigonal faces capped by diverse anions (i.e., S(2-) and CF3 SO3 (-) for compound 1, 2×CF3 SO3 (-) for compound 2, 2×NO3 (-) for compound 3, and tBuC6 H4 S(-) and Mo2 O7 (2-) for compound 4). This trigonal prism is bisected by another shrunken Ag3 trigon at its waist position. Interestingly, two inversion-related Ag9 trigonal-prismatic clusters are dimerized by the Mo2 O7 (2-) ion in compound 4. The twist is amplified by the bulkier thiolate, which also introduces high steric-hindrance for the capping ligand, that is, the longer dpph ligand. Four more silver-sulfur clusters (namely, compounds 5-8) with their nuclearity ranging from 6-10 were solely characterized by single-crystal X-ray diffraction to verify the above-described synergetic effect of mixed ligands in the construction of Ag9 twisted trigonal prisms. Surprisingly, only cluster 1 emits yellow luminescence at λ=584 nm at room temperature, which may be attributed to a charge transfer from the S 3p orbital to the Ag 5s orbital, or mixed with metal-centered (MC) d(10) →d(9) s(1) transitions. Upon cooling from 300 to 80 K, the emission intensity was enhanced along with a hypsochromic shift. The good linear relationship between the maximum emission intensity and the temperature for compound 1 in the range of 180-300 K indicates that this is a promising molecular luminescent

  10. The effects of monovalent and divalent cations on the stability of silver nanoparticles formed from direct reduction of silver ions by Suwannee River humic acid/natural organic matter

    International Nuclear Information System (INIS)

    The formation and characterization of AgNPs (silver nanoparticles) formed from the reduction of Ag+ by SRNOM (Suwannee River natural organic matter) is reported. The images of SRNOM-formed AgNPs and the selected area electron diffraction (SAED) were captured by high resolution transmission electron microscopy (HRTEM). The colloidal and chemical stability of SRNOM- and SRHA (Suwannee River humic acid)-formed AgNPs in different ionic strength solutions of NaCl, KCl, CaCl2 and MgCl2 was investigated in an effort to evaluate the key fate and transport processes of these nanoparticles in natural aqueous environments. The aggregation state, stability and sedimentation rate of the AgNPs were monitored by Dynamic Light Scattering (DLS), zeta potential, and UV–vis measurements. The results indicate that both types of AgNPs are very unstable in high ionic strength solutions. Interestingly, the nanoparticles appeared more unstable in divalent cation solutions than in monovalent cation solutions at similar concentrations. Furthermore, the presence of SRNOM and SRHA contributed to the nanoparticle instability at high ionic strength in divalent metallic cation solutions, most likely due to intermolecular bridging with the organic matter. The results clearly suggest that changes in solution chemistry greatly affect nanoparticle long term stability and transport in natural aqueous environments. Highlights: ► Formation of SRNOM-AgNPs under environmentally relevant conditions ► Influence of monovalent versus divalent cations on SRHA- and SRNOM-AgNP stability ► Effect of AgNPs on organic matter removal from water columns

  11. Controlled Distribution and Clustering of Silver in Ag-DLC Nanocomposite Coatings Using a Hybrid Plasma Approach.

    Science.gov (United States)

    Cloutier, M; Turgeon, S; Busby, Y; Tatoulian, M; Pireaux, J-J; Mantovani, D

    2016-08-17

    Incorporation of selected metallic elements into diamond-like carbon (DLC) has emerged as an innovative approach to add unique functional properties to DLC coatings, thus opening up a range of new potential applications in fields as diverse as sensors, tribology, and biomaterials. However, deposition by plasma techniques of metal-containing DLC coatings with well-defined structural properties and metal distribution is currently hindered by the limited understanding of their growth mechanisms. We report here a silver-incorporated diamond-like carbon coating (Ag-DLC) prepared in a hybrid plasma reactor which allowed independent control of the metal content and the carbon film structure and morphology. Morphological and chemical analyses of Ag-DLC films were performed by atomic force microscopy, scanning electron microscopy, and X-ray photoelectron spectroscopy. The vertical distribution of silver from the surface toward the coating bulk was found to be highly inhomogeneous due to top surface segregation and clustering of silver nanoparticles. Two plasma parameters, the sputtered Ag flux and ion energy, were shown to influence the spatial distribution of silver particles. On the basis of these findings, a mechanism for Ag-DLC growth by plasma was proposed. PMID:27454833

  12. Optical response of silver clusters and their hollow shells from linear-response TDDFT

    Science.gov (United States)

    Koval, Peter; Marchesin, Federico; Foerster, Dietrich; Sánchez-Portal, Daniel

    2016-06-01

    We present a study of the optical response of compact and hollow icosahedral clusters containing up to 868 silver atoms by means of time-dependent density functional theory. We have studied the dependence on size and morphology of both the sharp plasmonic resonance at 3-4 eV (originated mainly from sp-electrons), and the less studied broader feature appearing in the 6-7 eV range (interband transitions). An analysis of the effect of structural relaxations, as well as the choice of exchange correlation functional (local density versus generalised gradient approximations) both in the ground state and optical response calculations is also presented. We have further analysed the role of the different atom layers (surface versus inner layers) and the different orbital symmetries on the absorption cross-section for energies up to 8 eV. We have also studied the dependence on the number of atom layers in hollow structures. Shells formed by a single layer of atoms show a pronounced red shift of the main plasmon resonances that, however, rapidly converge to those of the compact structures as the number of layers is increased. The methods used to obtain these results are also carefully discussed. Our methodology is based on the use of localised basis (atomic orbitals, and atom-centered and dominant-product functions), which bring several computational advantages related to their relatively small size and the sparsity of the resulting matrices. Furthermore, the use of basis sets of atomic orbitals also allows the possibility of extending some of the standard population analysis tools (e.g. Mulliken population analysis) to the realm of optical excitations. Some examples of these analyses are described in the present work.

  13. Thorium and uranium carbide cluster cations in the gas phase: similarities and differences between thorium and uranium.

    Science.gov (United States)

    Pereira, Cláudia C L; Maurice, Rémi; Lucena, Ana F; Hu, Shuxian; Gonçalves, António P; Marçalo, Joaquim; Gibson, John K; Andrews, Lester; Gagliardi, Laura

    2013-10-01

    Laser ionization of AnC4 alloys (An = Th, U) yielded gas-phase molecular thorium and uranium carbide cluster cations of composition An(m)C(n)(+), with m = 1, n = 2-14, and m = 2, n = 3-18, as detected by Fourier transform ion-cyclotron-resonance mass spectrometry. In the case of thorium, Th(m)C(n)(+) cluster ions with m = 3-13 and n = 5-30 were also produced, with an intriguing high intensity of Th13C(n)(+) cations. The AnC13(+) ions also exhibited an unexpectedly high abundance, in contrast to the gradual decrease in the intensity of other AnC(n)(+) ions with increasing values of n. High abundances of AnC2(+) and AnC4(+) ions are consistent with enhanced stability due to strong metal-C2 bonds. Among the most abundant bimetallic ions was Th2C3(+) for thorium; in contrast, U2C4(+) was the most intense bimetallic for uranium, with essentially no U2C3(+) appearing. Density functional theory computations were performed to illuminate this distinction between thorium and uranium. The computational results revealed structural and energetic disparities for the An2C3(+) and An2C4(+) cluster ions, which elucidate the observed differing abundances of the bimetallic carbide ions. Particularly noteworthy is that the Th atoms are essentially equivalent in Th2C3(+), whereas there is a large asymmetry between the U atoms in U2C3(+).

  14. Ion-molecule clustering in differential mobility spectrometry: lessons learned from tetraalkylammonium cations and their isomers.

    Science.gov (United States)

    Campbell, J Larry; Zhu, Mabel; Hopkins, W Scott

    2014-09-01

    Differential mobility spectrometry (DMS) can distinguish ions based upon the differences in their high- and low-field ion mobilities as they experience the asymmetric waveform applied to the DMS cell. These mobilities are known to be influenced by the ions' structure, m/z, and charge distribution (i.e., resonance structures) within the ions themselves, as well as by the gas-phase environment of the DMS cell. While these associations have been developed over time through empirical observations, the exact role of ion structures or their interactions with clustering molecules remains generally unknown. In this study, that relationship is explored by observing the DMS behaviors of a series of tetraalkylammonium ions as a function of their structures and the gas-phase environment of the DMS cell. To support the DMS experiments, the basin-hopping search strategy was employed to identify candidate cluster structures for density functional theory treatment. More than a million cluster structures distributed across 72 different ion-molecule cluster systems were sampled to determine global minimum structures and cluster binding energies. This joint computational and experimental approach suggests that cluster geometry, in particular ion-molecule intermolecular separation, plays a critical role in DMS.

  15. Ab initio study of the structural, magnetic, and electronic properties of copper and silver clusters and their alloys with one palladium atom

    Directory of Open Access Journals (Sweden)

    S. J Hashemifar

    2015-01-01

    Full Text Available In this paper, the structural, magnetic, and electronic properties of two- to nine-atom copper and silver clusters and their alloys with one palladium atom are investigated by using full-potential all-electron density functional computations. After calculating minimized energy of several structural isomers of every nanocluster, it is argued that the small size nanoclusters (up to size of 6, ‎ prefer planar structures, while by increasing size a 2D-3D structural transformation is observed. The structural transformation of pure and copper-palladium clusters occurs in the size of seven and that of silver-palladium cluster in happens at the size of six. The calculated second difference and dissociation energies confirm that the two- and eight- atom pure clusters and three- and seven- atom alloyed clusters are magic clusters. The electronic and magnetic properties of stable isomers are calculated and considered after applying many body based GW correction.

  16. A density functional study of silver clusters on a stepped graphite surface: formation of self-assembled nano-wires.

    Science.gov (United States)

    Singh, Akansha; Sen, Prasenjit

    2015-05-21

    Adsorption and diffusion of silver adatoms and clusters containing up to eight atoms on an HOPG substrate with an armchair step are studied using density functional methods. Step edges act as attractive sinks for adatoms and clusters. The diffusion barrier of an Ag adatom along the step edge is much larger than that on a clean terrace. At zero temperature, Ag clusters either distort or dissociate by forming covalent bonds with the edge C atoms. At 600 K, Ag5 and Ag8 clusters diffuse to the step edges, and then break up so as to maximize Ag-C bonds. The Ag atoms try to form a nanowire structure along the step edge. At such high temperatures, diffusion of clusters along the step edge involves diffusion of individual Ag atoms not bonded to the edge C atoms. Assumption of complete immobility of clusters trapped at step edges in the Gates-Robins model is not valid at high temperatures in this particular system. PMID:25903308

  17. A cationic copper(I) iodide cluster MOF exhibiting unusual ligand assisted thermochromism.

    Science.gov (United States)

    Yadav, Ashok; Srivastava, Anant Kumar; Balamurugan, Ayyakkalai; Boomishankar, Ramamoorthy

    2014-06-14

    By employing a tridentate thiophosphoramide ligand, [(NHAQ)3P[double bond, length as m-dash]S] (AQ = 3-quinolinyl), a cationic MOF, {[Cu6I5(L(1))2](OH)·3DMF·2.5MeOH}n, was synthesized. Photo-physical studies on the 2D-MOF showed an unusual thermochromic behaviour emitting a blue fluorescence at 298 K due to the AQ chromophore and an orange-yellow phosphorescence at 77 K due to the [Cu6I5](+) unit. PMID:24760039

  18. Ferromagnetic spin coupling in the chromium dimer cation: Measurements by photodissociation spectroscopy combined with coupled-cluster calculations

    Energy Technology Data Exchange (ETDEWEB)

    Egashira, Kazuhiro, E-mail: egashira@clusterlab.jp [East Tokyo Laboratory, Genesis Research Institute, Inc., 717-86 Futamata, Ichikawa, Chiba 272-0001 (Japan); Yamada, Yurika; Kita, Yukiumi; Tachikawa, Masanori [Quantum Chemistry Division, Yokohama City University, Seto 22-2, Kanazawa-ku, Yokohama 236-0027 (Japan)

    2015-02-07

    The magnetic coupling of the chromium dimer cation, Cr{sub 2}{sup +}, has been an outstanding problem for decades. An optical absorption spectrum of Cr{sub 2}{sup +} has been obtained by photodissociation spectroscopy in the photon-energy range from 2.0 to 5.0 eV. Besides, calculations have been performed by the equation-of-motion coupled-cluster singles and doubles method for vertical excitation of the species. Their coincidence supports our assignment that the ground electronic state exhibits a ferromagnetic spin coupling, which is contrary to those of neutral and negatively charged dimers, Cr{sub 2} and Cr{sub 2}{sup −}, in their lowest spin states.

  19. Structure and photoabsorption properties of cationic alkali dimers solvated in neon clusters.

    Science.gov (United States)

    Zanuttini, D; Douady, J; Jacquet, E; Giglio, E; Gervais, B

    2010-11-01

    We present a theoretical investigation of the structure and optical absorption of M(2)(+) alkali dimers (M=Li,Na,K) solvated in Ne(n) clusters for n=1 to a few tens Ne atoms. For all these alkali, the lowest-energy isomers are obtained by aggregation of the first Ne atoms at the extremity of the alkali molecule. This particular geometry, common to other M(2)(+)-rare gas clusters, is intimately related to the shape of the electronic density of the X  (2)Σ(g)(+) ground state of the bare M(2)(+) molecules. The structure of the first solvation shell presents equilateral Ne(3) and capped pentagonal Ne(6) motifs, which are characteristic of pure rare gas clusters. The size and geometry of the complete solvation shell depend on the alkali and were obtained at n=22 with a D(4h) symmetry for Li and at n=27 with a D(5h) symmetry for Na. For K, our study suggests that the closure of the first solvation shell occurs well beyond n=36. We show that the atomic arrangement of these clusters has a profound influence on their optical absorption spectrum. In particular, the XΣ transition from the X  (2)Σ(g)(+) ground state to the first excited (2)Σ(u)(+) state is strongly blueshifted in the Frank-Condon area.

  20. Heterogeneous Solvatochromism of Fluorescent DNA-Stabilized Silver Clusters Precludes Use of Simple Onsager-Based Stokes Shift Models.

    Science.gov (United States)

    Copp, Stacy M; Faris, Alexis; Swasey, Steven M; Gwinn, Elisabeth G

    2016-02-18

    The diverse optical and chemical properties of DNA-stabilized silver clusters (AgN-DNAs) have challenged the development of a common model for these sequence-tunable fluorophores. Although correlations between cluster geometry and fluorescence color have begun to shed light on how the optical properties of AgN-DNAs are selected, the exact mechanisms responsible for fluorescence remain unknown. To explore these mechanisms, we study four distinct purified AgN-DNAs in ethanol-water and methanol-water mixtures and find that the solvatochromic behavior of AgN-DNAs varies widely among different cluster species and differs markedly from prior results on impure material. Placing AgN-DNAs within the context of standard Lippert-Mataga solvatochromism models based on the Onsager reaction field, we show that such nonspecific solvent models are not universally applicable to AgN-DNAs. Instead, alcohol-induced solvatochromism of AgN-DNAs may be governed by changes in hydration of the DNA template, with spectral shifts resulting from cluster shape changes and/or dielectric changes in the local vicinity of the cluster.

  1. Validation of Methods for Computational Catalyst Design: Geometries, Structures, and Energies of Neutral and Charged Silver Clusters

    Energy Technology Data Exchange (ETDEWEB)

    Duanmu, Kaining; Truhlar, Donald G.

    2015-04-30

    We report a systematic study of small silver clusters, Agn, Agn+, and Agn–, n = 1–7. We studied all possible isomers of clusters with n = 5–7. We tested 42 exchange–correlation functionals, and we assess these functionals for their accuracy in three respects: geometries (quantitative prediction of internuclear distances), structures (the nature of the lowest-energy structure, for example, whether it is planar or nonplanar), and energies. We find that the ingredients of exchange–correlation functionals are indicators of their success in predicting geometries and structures: local exchange–correlation functionals are generally better than hybrid functionals for geometries; functionals depending on kinetic energy density are the best for predicting the lowest-energy isomer correctly, especially for predicting two-dimensional to three-dimenstional transitions correctly. The accuracy for energies is less sensitive to the ingredient list. Our findings could be useful for guiding the selection of methods for computational catalyst design.

  2. Crystal structure and solid-state properties of discrete hexa cationic trinuclear zinc triazole cluster

    Indian Academy of Sciences (India)

    Chatla Naga Babu; Paladugu Suresh; Arruri Sathyanarayana; Prasenjit Das; Ganesan Prabusankar

    2015-08-01

    A linear trinuclear cluster of the type [{Zn3 (HTrz)6 (H2O)6}6+ (NO$_{3}^{−}$)6 (H2O)] (ZnT) has been synthesized by one-pot reaction between 1,2,4-triazole and Zn(NO3).6H2O. Molecule consists of three Zn2+ ions linearly connected by 1,2,4-triazole with tri-fold symmetry. The coordination geometry around the zinc centre is octahedral with zinc-zinc separation of 3.810 Å. The coordination environment of central Zn2+ ion is satisfied by nitrogen atoms of six 1,2,4-triazoles, while the geometry of terminal Zn2+ ions is fulfilled by nitrogen atoms of three 1,2,4-triazoles and three water molecules. The thermal and absorption properties of ZnT have been reported for the first time.

  3. Synthesis and characterization of silver diethyldithiocarbamate cluster for the deposition of acanthite (Ag2S) thin films for photoelectrochemical applications

    International Nuclear Information System (INIS)

    Acanthite (Ag2S) thin films were fabricated on fluorine doped tin oxide coated conducting glass substrates by aerosol assisted chemical vapor deposition (AACVD) using silver cluster [Ag4{S2CN(C2H5)2}3(C5H5N)2]n·nNO3·2nH2O (1) [where (S2CN(C2H5)2) = diethyldithiocarbamate, C5H5N = pyridine] as a single source precursor. Cluster (1) was synthesized by the reaction of sodium diethyldithiocarbamate with silver nitrate in a mixture of acetone and pyridine. (1) was analyzed by melting point, elemental analysis, Fourier transform infrared spectroscopy, proton nuclear magnetic resonance spectroscopy, thermogravimetry and single crystal X-ray studies. Single crystal X-ray studies showed that (1) crystallizes in the triclinic crystal system with a = 11.4372(3), b = 11.6768(3), and c = 16.3672(4) Å and α = 105.817(3), β = 97.891(3), and γ = 93.274(3)° in the space group P-1. Thermogravimetric analysis revealed that (1) undergoes facile thermal decomposition at 400 °C to give a stable residual mass consistent with the formation of Ag2S. Thin films grown from a 0.02 M solution of (1) in pyridine at 350 and 400 °C using AACVD technique were characterized by powder X-ray diffraction, field emission scanning electron microscopy (FESEM), energy dispersive X-ray and ultraviolet-visible spectrophotometry. FESEM images of the films exhibited well-defined nanorods with length > 1000 nm and diameter 100–150 nm grown without any cracks, fractures or directional preference. A band gap of 1.05 eV was estimated by extrapolating the linear part of a Tauc plot recorded for the films. The photoelectrochemical (PEC) characteristics recorded under Air Mass 1.5 illumination indicated a photocurrent density of 220 μA cm−2 at 0.0 V vs Ag/AgCl/3 M KCl. The optical and PEC characteristics of the deposited thin films proved their suitability for PEC applications. - Highlights: • Synthesis and characterization of silver diethyl dithiocarbamate cluster • Fabrication of optically

  4. Clustered Conserved Cysteines in Hyaluronan Synthase Mediate Cooperative Activation by Mg(2+) Ions and Severe Inhibitory Effects of Divalent Cations.

    Science.gov (United States)

    Tlapak-Simmons, Valarie L; Medina, Andria P; Baggenstoss, Bruce A; Nguyen, Long; Baron, Christina A; Weigel, Paul H

    2011-11-15

    Hyaluronan synthase (HAS) uses UDP-GlcUA and UDP-GlcNAc to make hyaluronan (HA). Streptococcus equisimilis HAS (SeHAS) contains four conserved cysteines clustered near the membrane, and requires phospholipids and Mg(2+) for activity. Activity of membrane-bound or purified enzyme displayed a sigmoidal saturation profile for Mg(2+) with a Hill coefficient of 2. To assess if Cys residues are important for cooperativity we examined the Mg(2+) dependence of mutants with various combinations of Cys-to-Ala mutations. All Cys-mutants lost the cooperative response to Mg(2+). In the presence of Mg(2+), other divalent cations inhibited SeHAS with different potencies (Cu(2+)~Zn(2+) >Co(2+) >Ni(2+) >Mn(2+) >Ba(2+) Sr(2+) Ca(2+)). Some divalent metal ions likely inhibit by displacement of Mg(2+)-UDP-Sugar complexes (e.g. Ca(2+), Sr(2+) and Ba(2+) had apparent Ki values of 2-5 mM). In contrast, Zn(2+) and Cu(2+) inhibited more potently (apparent Ki ≤ 0.2 mM). Inhibition of Cys-null SeHAS by Cu(2+), but not Zn(2+), was greatly attenuated compared to wildtype. Double and triple Cys-mutants showed differing sensitivities to Zn(2+) or Cu(2+). Wildtype SeHAS allowed to make HA prior to exposure to Zn(2+) or Cu(2+) was protected from inhibition, indicating that access of metal ions to sensitive functional groups was hindered in processively acting HA•HAS complexes. We conclude that clustered Cys residues mediate cooperative interactions with Mg(2+) and that transition metal ions inhibit SeHAS very potently by interacting with one or more of these -SH groups.

  5. Adsorption of a single gold or silver atom on vanadium oxide clusters.

    Science.gov (United States)

    Ding, Xun-Lei; Wang, Dan; Li, Rui-Jie; Liao, Heng-Lu; Zhang, Yan; Zhang, Hua-Yong

    2016-04-14

    The bonding properties between a single atom and its support have a close relationship with the stability and reactivity of single-atom catalysts. As a model system, the structural and electronic properties of bimetallic oxide clusters MV3Oy(q) (M = Au or Ag, q = 0, ±1, and y = 6-8) are systematically studied using density functional theory. The single noble metal atom Au or Ag tends to be adsorbed on the periphery of the V oxide clusters. Au prefers V sites for oxygen-poor clusters and O sites for oxygen-rich clusters, while Ag prefers O sites for most cases. According to natural population analysis, Au may possess positive or negative charges in the bimetallic oxide clusters, while Ag usually possesses positive charges. The bonding between Au and V has relatively high covalent character according to the bond order analysis. This work may provide some clues for understanding the bonding properties of single noble metal atoms on the support in practical single-atom catalysts, and serve as a starting point for further theoretical studies on the reaction mechanisms of related catalytic systems.

  6. Silver clusters insert into polymer solar cell for enhancing light absorption

    Institute of Scientific and Technical Information of China (English)

    Guolong Li; Hongyu Zhen; Zhuoyin Huang; Kan Li; Weidong Shen; Xu Liu

    2012-01-01

    As an employment of surface plasmonic effect,the consequence of insertion of a layer of Ag clusters into polymer solar cell on the enhancement of light absorption and power conversion efficiency is investigated.Optical analysis based on the finite-difference time-domain (FDTD) is performed with experiments to evaluate the effect of the interaction between the Ag clusters and incident light on light absorption in polymer solar cell Ag clusters modify the light wave vector and the electromagnetic field inside the device is redistributed and enhanced.As a result,polymer solar cells achieve an overall increase in absorption,short-circuit current density,and power conversion efficiency.

  7. Media effects on the optical absorption spectra of silver clusters embedded in rara gas matrices

    International Nuclear Information System (INIS)

    The optical absorption of small mass selected Agn-clusters (n=7, 11, 15, 21) embedded in solid Ar, Kr and Xe has been measured. The absorption spectra show 1 to 3 major peaks between 3 and 4.5 eV, depending on the cluster size. Changing the matrix gas Ar→Kr→Xe induces a redshift which is comparable for all sizes studied and does not affect the main structure of the absorption spectra. We propose a scheme to estimate the gas phase value of the absorption energies which is in fair agreement with an estimation obtained by a simple model based on a Drude metal. (author). 10 refs, 2 figs

  8. Two reaction regimes in the oxidation of larger cationic tantalum clusters (Tan(+), n = 13-40) under multi-collision conditions.

    Science.gov (United States)

    Neuwirth, D; Eckhard, J F; Visser, B R; Tschurl, M; Heiz, U

    2016-03-21

    The reaction of cationic tantalum clusters (Tan(+), n = 13-40) with molecular oxygen is studied under multi-collision conditions and at different temperatures. Consecutive reaction proceeds in several steps upon subsequent attachment of O2. All cluster sizes exhibit fast reaction with oxygen and form a characteristic final reaction product. The time-dependent product analysis enables the fitting to a kinetic model with the extraction of all the rate constants. Determined rate constants reveal the existence of two different regimes, which are interpreted as a change in the reaction mechanism. Based on the temperature-dependent reaction behavior, it is proposed that the reaction changes from a dissociative to a molecular adsorption of oxygen on the clusters. It is found that both regimes appear for all cluster sizes, but the transition takes place at different intermediate oxides TanOx(+). In general it is observed that transition occurs later for larger clusters, which is attributed to an increased cluster surface. PMID:26924176

  9. Neutral and cationic free-space oxygen–silicon clusters SiO{sub n} (1

    Energy Technology Data Exchange (ETDEWEB)

    Forte, G. [Dipartimento di Scienze del Farmaco, Facoltà di Farmacia, Università di Catania, Viale A. Doria, 6, I-95126 Catania (Italy); Angilella, G.G.N., E-mail: giuseppe.angilella@ct.infn.it [Dipartimento di Fisica e Astronomia, Università di Catania, 64, Via S. Sofia, I-95123 Catania (Italy); Scuola Superiore di Catania, Università di Catania, Via S. Nullo, 5/i, I-95123 Catania (Italy); CNISM, UdR Catania, 64, Via S. Sofia, I-95123 Catania (Italy); INFN, Sezione di Catania, 64, Via S. Sofia, I-95123 Catania (Italy); Pittalà, V. [Dipartimento di Scienze del Farmaco, Facoltà di Farmacia, Università di Catania, Viale A. Doria, 6, I-95126 Catania (Italy); March, N.H. [Department of Physics, University of Antwerp, Groenenborgerlaan 171, B-2020 Antwerp (Belgium); Oxford University, Oxford (United Kingdom); Pucci, R. [Dipartimento di Fisica e Astronomia, Università di Catania, 64, Via S. Sofia, I-95123 Catania (Italy); CNISM, UdR Catania, 64, Via S. Sofia, I-95123 Catania (Italy)

    2012-01-09

    Motivated by the theoretical study of Saito and Ono (2011) on three crystalline forms of SiO{sub 2} under pressure, quantum-chemical calculations on various free-space clusters of SiO{sub n} and GeO{sub n} for 1cationic clusters have been examined, for both geometry and equilibrium bond lengths. Coupled clusters and correlation-corrected MP2 calculations are presented. For the cations, we emphasize especially the structural distortions occurring in removing degeneracies. -- Highlights: ► Geometry and structure of various SiO{sub n} and GeO{sub n} clusters. ► Both neutral and cationic clusters. ► Varying coordination numbers. ► Relevant for high pressure studies.

  10. Silver-cobalt mineralization in the Upper Seymchan ore cluster, Northeastern Russia

    Science.gov (United States)

    Goryachev, N. A.; Gamyanin, G. N.; Prokof'ev, V. Yu.; Savva, N. E.; Velivetskaya, T. A.; Ignat'ev, A. V.

    2014-09-01

    This paper is focused on the Early Cretaceous Ag-Bi-Co-sulfoarsenide mineralization atypical of northeastern Asia, which contains diverse Co-Ni sulfoarsenides, Se-bearing Bi sulfotellurites, and Ag-Bi-Pb sulfosalts. The Upper Seymchan ore cluster is located at the boundary between the Paleozoic Omulevka Terrane of carbonate platform and the In'yali-Debin Synclinorium of the Kular-Nera Terrane. These ore-bearing sequences are represented by the Middle Jurassic terrigenous rocks that rest upon the Upper Triassic sandshale rocks of the upper structural stage. The sedimentary rocks are cut through by high-Al granitic plutons and younger granite-porphyry dikes. The orebodies that are superposed on igneous rocks were formed during (1) the quartz-chlorite-tourmaline stage of metasomatic alteration, (2) the main economic tourmaline-chlorite-quartz-sulfoarsenide vein stage, (3) the polysulfide-quartz stage with Ag, Se, Bi minerals, and (4) the postore quartz-calcite stage with fluorite. The epithermal veins of festoon chalcedony-like quartz with Sb-bearing arsenopyrite occupy a special position. In particular orebodies, the chlorite-quartz ore veins dominate at the upper levels, whereas the quartz-tourmaline veins occur at the lower levels. Wall-rock alteration is represented by metasomatic chloritization and tourmalinization up to the formation of monomineralic metasomatic zones. Sulfides and sulfoarsenides are distinguished by anomalous enrichment of sulfur in the light isotope (δ34S = -12.8 to -16.7‰) in contrast to the sulfur isotopic composition of Sb-asenopyrite (-1.7‰) from the genetically different epithermal veins. The oxygen isotopic composition of calcite (the third stage) is uniform at all studied deposits and reveals a tendency to updip enrichment in δ18O within a vertical interval of 200 m. Quartz from ore-bearing and epithermal veins has an almost identical δ18O value (±2‰) but differs from quartz at the tin deposits related to granites of the

  11. Investigation of the NH-π hydrogen bond interaction in the aniline-alkene (C2H4,C3H6,C4H8) cluster cations by infrared depletion spectroscopy

    International Nuclear Information System (INIS)

    The vibrational spectra of the NH stretching vibrations of aniline-alkene cluster cations have been measured using infrared depletion method. Aniline-ethene cation showed three strong absorption bands at 3448, 3314 and 3220 cm-1. The comparison with MO calculation has shown that the main intermolecular interaction is the NH-π type hydrogen bond between one of the NH bonds of aniline cation and π-electron of ethene, which is different from that observed for the neutral aniline-ethene cluster. The bands at 3448 and 3220 cm-1 have been assigned to the stretching vibrations of free NH and bonded NH, respectively, and the band at 3314 cm-1 to the binary overtone of the NH2 deformation vibration. Similar results have been obtained for aniline-propene and aniline-butene cluster cations. The red shift of the stretching vibration of free NH bond of aniline cation agreed with that expected from the correlation with the proton affinity of the acceptor molecule obtained for the aniline-aromatic cluster cations (NH-π type)

  12. Design and synthesis of a cyclitol-derived scaffold with axial pyridyl appendages and its encapsulation of the silver(I) cation

    OpenAIRE

    Pierre-Marc Léo; Christophe Morin; Christian Philouze

    2010-01-01

    Conversion of a myo-inositol derivative into a scyllo-inositol-derived scaffold with C3v symmetry bearing three axial pyridyl appendages is presented. This pre-organized hexadentate ligand allows complexation of silver(I). The crystal structure of the complex was established.

  13. ToF-SIMS and laser-SNMS analysis of Madin-Darby canine kidney II cells with silver nanoparticles using an argon cluster ion beam.

    Science.gov (United States)

    Nees, Ricarda; Pelster, Andreas; Körsgen, Martin; Jungnickel, Harald; Luch, Andreas; Galla, Hans-Joachim; Arlinghaus, Heinrich F

    2016-06-01

    The use of nanoparticles is one of the fastest expanding fields in industrial as well as in medical applications, owing to their remarkable characteristics. Silver nanoparticles (AgNPs) are among the most-commercialized nanoparticles because of their antibacterial effects. Laser postionization secondary neutral mass spectrometry (laser-SNMS) and time-of-flight secondary ion mass spectrometry in combination with argon cluster ion sputtering was used for the first time to investigate the effects of AgNPs on Madin-Darby canine kidney (MDCK) II cells. Depth profiles and high-resolution three dimensional (3D) images of nanoparticles and organic compounds from cells were obtained using an Ar cluster ion beam for sputtering and Bi3 (+) primary ions for the analysis. The 3D distribution of AgNPs and other organic compounds in MDCK II cells could be readily detected with very high efficiency, sensitivity, and submicron lateral resolution. The argon cluster ion beam is well suited for the sputtering of biological samples. It enables a high sample removal rate along with low molecular degradation. The outer membrane, the cytoplasm, and the nuclei of the cells could be clearly visualized using the signals PO(+) and C3H8N(+) or CN(+) and C3H8N(+). The laser-SNMS images showed unambiguously that AgNPs are incorporated by MDCK II cells and often form silver aggregates with a diameter of a few micrometers, mainly close to the outside of the cell nuclei. PMID:26671480

  14. A comparative study on geometries, stabilities, and electronic properties between bimetallic AgnX (X=Au, Cu; n=1-8) and pure silver clusters

    Institute of Scientific and Technical Information of China (English)

    Ding Li-Ping; Kuang Xiao-Yu; Shao Peng; Zhao Ya-Ru; Li Yah-Fang

    2012-01-01

    Using the meta-generalized gradient approximation (meta-GGA) exchange correlation TPSS functional,the geometric structures,the relative stabilities,and the electronic properties of bimetallic AgnX (X=Au,Cu; n=l-8) clusters are systematically investigated and compared with those of pure silver clusters.The optimized structures show that the transition point from preferentially planar to three-dimensional structure occurs at n =6 for the AgnAu clusters,and at n =5 for AgnCu clusters.For different-sized AgnX clusters,one X (X=Au or Cu) atom substituted Agn+1 structure is a dominant growth pattern.The calculated fragmentation energies,second-order differences in energies,and the highest occupied molecular orbital-lowest unoccupied molecular orbital (HOMO-LUMO) energy gaps show interesting odd-even oscillation behaviours,indicating that Ag2,4,6,8 and Ag1,3,5,7X (X=Au,Cu) clusters keep high stabilities in comparison with their neighbouring clusters.The natural population analysis reveals that the charges transfer from the Agn host to the impurity atom except for the Ag2Cu cluster.Moreover,vertical ionization potential (VIP),vertical electronic affinity (VEA),and chemical hardness (η) are discussed and compared in depth.The same odd-even oscillations are found for the VIP and ηof the AgnX (X=Au,Cu; n=1-8) clusters.

  15. Structure, magnetism, and dissociation energy of small bimetallic cobalt-chromium oxide cluster cations: A density-functional-theory study

    Science.gov (United States)

    Pham, Hung Tan; Cuong, Ngo Tuan; Tam, Nguyen Minh; Lam, Vu Dinh; Tung, Nguyen Thanh

    2016-01-01

    We study CoxCryOm+ (x + y = 2, 3 and 1 ≤ m ≤ 4) clusters by means of density-functional-theory calculations. It is found that the clusters grow preferentially through maximizing the number of metal-oxygen bonds with a favor on Cr sites. The size- and composition-dependent magnetic behavior is discussed in relation with the local atomic magnetic moments. While doped species show an oscillatory magnetic behavior, the total magnetic moment of pure cobalt and chromium oxide clusters tends to enhance or reduce as increasing the oxygen content, respectively. The dissociation energies for different evaporation channels are also calculated to suggest the stable patterns, as fingerprints for future photofragmentation experiments.

  16. Photoionization of cold gas phase coronene and its clusters: Autoionization resonances in monomer, dimer, and trimer and electronic structure of monomer cation

    International Nuclear Information System (INIS)

    Polycyclic aromatic hydrocarbons (PAHs) are key species encountered in a large variety of environments such as the Interstellar Medium (ISM) and in combustion media. Their UV spectroscopy and photodynamics in neutral and cationic forms are important to investigate in order to learn about their structure, formation mechanisms, and reactivity. Here, we report an experimental photoelectron-photoion coincidence study of a prototypical PAH molecule, coronene, and its small clusters, in a molecular beam using the vacuum ultraviolet (VUV) photons provided by the SOLEIL synchrotron facility. Mass-selected high resolution threshold photoelectron (TPES) and total ion yield spectra were obtained and analyzed in detail. Intense series of autoionizing resonances have been characterized as originating from the monomer, dimer, and trimer neutral species, which may be used as spectral fingerprints for their detection in the ISM by VUV absorption spectroscopy. Finally, a full description of the electronic structure of the monomer cation was made and discussed in detail in relation to previous spectroscopic optical absorption data. Tentative vibrational assignments in the near-threshold TPES spectrum of the monomer have been made with the support of a theoretical approach based on density functional theory

  17. Photoionization of cold gas phase coronene and its clusters: autoionization resonances in monomer, dimer, and trimer and electronic structure of monomer cation.

    Science.gov (United States)

    Bréchignac, Philippe; Garcia, Gustavo A; Falvo, Cyril; Joblin, Christine; Kokkin, Damian; Bonnamy, Anthony; Parneix, Pascal; Pino, Thomas; Pirali, Olivier; Mulas, Giacomo; Nahon, Laurent

    2014-10-28

    Polycyclic aromatic hydrocarbons (PAHs) are key species encountered in a large variety of environments such as the Interstellar Medium (ISM) and in combustion media. Their UV spectroscopy and photodynamics in neutral and cationic forms are important to investigate in order to learn about their structure, formation mechanisms, and reactivity. Here, we report an experimental photoelectron-photoion coincidence study of a prototypical PAH molecule, coronene, and its small clusters, in a molecular beam using the vacuum ultraviolet (VUV) photons provided by the SOLEIL synchrotron facility. Mass-selected high resolution threshold photoelectron (TPES) and total ion yield spectra were obtained and analyzed in detail. Intense series of autoionizing resonances have been characterized as originating from the monomer, dimer, and trimer neutral species, which may be used as spectral fingerprints for their detection in the ISM by VUV absorption spectroscopy. Finally, a full description of the electronic structure of the monomer cation was made and discussed in detail in relation to previous spectroscopic optical absorption data. Tentative vibrational assignments in the near-threshold TPES spectrum of the monomer have been made with the support of a theoretical approach based on density functional theory. PMID:25362317

  18. Photoionization of cold gas phase coronene and its clusters: Autoionization resonances in monomer, dimer, and trimer and electronic structure of monomer cation

    Energy Technology Data Exchange (ETDEWEB)

    Bréchignac, Philippe, E-mail: philippe.brechignac@u-psud.fr; Falvo, Cyril; Parneix, Pascal; Pino, Thomas; Pirali, Olivier [Institut des Sciences Moléculaires d’Orsay, CNRS UMR8214, Univ Paris-Sud, F-91405 Orsay (France); Garcia, Gustavo A.; Nahon, Laurent [Synchrotron SOLEIL, L’Orme des Merisiers, Saint-Aubin, B.P. 48, F-91192 Gif-sur-Yvette (France); Joblin, Christine; Kokkin, Damian; Bonnamy, Anthony [IRAP, Université de Toulouse 3 - CNRS, 9 Av. Colonel Roche, B.P. 44346, F-31028 Toulouse Cedex 4 (France); Mulas, Giacomo [INAF - Osservatorio Astronomico di Cagliari, via della scienza 5, I-09047 Selargius (Italy)

    2014-10-28

    Polycyclic aromatic hydrocarbons (PAHs) are key species encountered in a large variety of environments such as the Interstellar Medium (ISM) and in combustion media. Their UV spectroscopy and photodynamics in neutral and cationic forms are important to investigate in order to learn about their structure, formation mechanisms, and reactivity. Here, we report an experimental photoelectron-photoion coincidence study of a prototypical PAH molecule, coronene, and its small clusters, in a molecular beam using the vacuum ultraviolet (VUV) photons provided by the SOLEIL synchrotron facility. Mass-selected high resolution threshold photoelectron (TPES) and total ion yield spectra were obtained and analyzed in detail. Intense series of autoionizing resonances have been characterized as originating from the monomer, dimer, and trimer neutral species, which may be used as spectral fingerprints for their detection in the ISM by VUV absorption spectroscopy. Finally, a full description of the electronic structure of the monomer cation was made and discussed in detail in relation to previous spectroscopic optical absorption data. Tentative vibrational assignments in the near-threshold TPES spectrum of the monomer have been made with the support of a theoretical approach based on density functional theory.

  19. The effects of cation-anion clustering on defect migration in MgAl2O4.

    Science.gov (United States)

    Zamora, Richard J; Voter, Arthur F; Perez, Danny; Perriot, Romain; Uberuaga, Blas P

    2016-07-20

    Magnesium aluminate spinel (MgAl2O4), like many other ceramic materials, offers a range of technological applications, from nuclear reactor materials to military body armor. For many of these applications, it is critical to understand both the formation and evolution of lattice defects throughout the lifetime of the material. We use the Speculatively Parallel Temperature Accelerated Dynamics (SpecTAD) method to investigate the effects of di-vacancy and di-interstitial formation on the mobility of the component defects. From long-time trajectories of the state-to-state dynamics, we characterize the migration pathways of defect clusters, and calculate their self-diffusion constants across a range of temperatures. We find that the clustering of Al and O vacancies drastically reduces the mobility of both defects, while the clustering of Mg and O vacancies completely immobilizes them. For interstitials, we find that the clustering of Mg and O defects greatly reduces O interstitial mobility, but has only a weak effect on Mg. These findings illuminate important new details regarding defect kinetics relevant to the application of MgAl2O4 in extreme environments.

  20. The structure of lithium garnets: cation disorder and clustering in a new family of fast Li+ conductors.

    Science.gov (United States)

    Cussen, Edmund J

    2006-01-28

    The structure of the fast lithium-ion conducting garnets Li5La3M2O12 (M = Ta, Nb) reveals Li+ on both tetrahedral and octahedral sites and suggests that the latter are responsible for the observed Li+ mobility via a clustering mechanism. PMID:16493817

  1. 2D-3D Transition for Cationic and Anionic Gold Clusters: A Kinetic Energy Density Functional Study

    DEFF Research Database (Denmark)

    Ferrighi, Lara; Hammer, Bjørk; Madsen, Georg

    2009-01-01

    We present a density functional theory study of the energetics of isolated Aun+ (n = 5-10) and Aun- (n = 8-13) gold clusters. We compare our results to both theoretical and experimental values from the literature and find the use of meta-generalized gradient approximation (MGGA) functionals...

  2. Heterolysis of Dihydrogen by Silver Alkoxides and Fluorides.

    Science.gov (United States)

    Tate, Brandon K; Nguyen, Jenna T; Bacsa, John; Sadighi, Joseph P

    2015-07-01

    Alkoxide-bridged disilver cations react with dihydrogen to form hydride-bridged cations, releasing free alcohol. Hydrogenolysis of neutral silver fluorides affords hydride-bridged disilver cations as their bifluoride salts. These reactions proceed most efficiently when the supporting ligands are expanded N-heterocyclic carbenes (NHCs) derived from 6- and 7-membered cyclic amidinium salts. Kinetics studies show that silver fluoride hydrogenolysis is first-order in both silver and dihydrogen.

  3. A cation exchange method for separation of 111In from inactive silver, copper, traces of iron and radioactive gallium and zinc isotopes

    International Nuclear Information System (INIS)

    111In was produced by the 109Ag(α, 2n)111In reaction. A simple radiochemical separation technique, using Dowex-50 cation exchange resin (with prior removal of copper bulk, if present), has been employed to separate radioindium from inactive contaminants like Ag, Cu, Fe and active contaminant like 67Ga and 65Zn. The radiochemical separation yield was 90-99%. The radionuclide purity of 111In was >99% at 60 h after EOB. The level of all the inactive contaminants was <5 μg/mL in the final product. (Author)

  4. DFT-D Investigation of the Interaction Between Ir(III) Based Photosensitizers and Small Silver Clusters Ag$_n$ ($n$=2-20, 92)

    CERN Document Server

    Bokareva, Olga S

    2013-01-01

    A dispersion-corrected density functional theory study of the photosensitizer [Ir(ppy)$_2$(bpy)]$^+$ and its derivatives bound to silver clusters Ag$_n$ ($n$=2-20, 92) is performed. The goal is to provide a new system-specific set of $C_{\\rm 6}^{}$ interaction parameters for Ag and Ir atoms. To this end a QM:QM scheme is employed using the PBE functional and RPA as well as MP2 calculation as a reference. The obtained $C_{\\rm 6}^{}$ coefficients were applied to calculate dissociation curves of selected IrPS-Ag$_n$ complexes and binding energies of derivatives containing oxygen and sulphur as heteroatoms in the ligands. Comparing different $C_{\\rm 6}^{}$ parameters it is concluded that RPA-based dispersion correction produces binding energies close to standard D2 and D3 models, whereas MP2-derived parameters overestimate these energies.

  5. Synthesis, structure and gas-phase reactivity of the mixed silver hydride borohydride nanocluster [Ag3(μ3-H)(μ3-BH4)L(Ph)3]BF4 (L(Ph) = bis(diphenylphosphino)methane).

    Science.gov (United States)

    Zavras, Athanasios; Ariafard, Alireza; Khairallah, George N; White, Jonathan M; Mulder, Roger J; Canty, Allan J; O'Hair, Richard A J

    2015-11-21

    Borohydrides react with silver salts to give products that span multiple scales ranging from discrete mononuclear compounds through to silver nanoparticles and colloids. The cluster cations [Ag3(H)(BH4)L3](+) are observed upon electrospray ionization mass spectrometry of solutions containing sodium borohydride, silver(I) tetrafluoroborate and bis(dimethylphosphino)methane (L(Me)) or bis(diphenylphosphino)methane (L(Ph)). By adding NaBH4 to an acetonitrile solution of AgBF4 and L(Ph), cooled to ca. -10 °C, we have been able to isolate the first mixed silver hydride borohydride nanocluster, [Ag3(μ3-H)(μ3-BH4)L(Ph)3]BF4, and structurally characterise it via X-ray crystallography. Combined gas-phase experiments (L(Me) and L(Ph)) and DFT calculations (L(Me)) reveal how loss of a ligand from the cationic complexes [Ag3(H)(BH4)L3](+) provides a change in geometry that facilitates subsequent loss of BH3 to produce the dihydride clusters, [Ag3(H)2Ln](+) (n = 1 and 2). Together with the results of previous studies (Girod et al., Chem. - Eur. J., 2014, 20, 16626), this provides a direct link between mixed silver hydride/borohydride nanoclusters, silver hydride nanoclusters, and silver nanoclusters.

  6. Spectroscopic Properties of Novel Aromatic Metal Clusters: NaM4 (M=Al, Ga, In) and their Cations and Anions

    Energy Technology Data Exchange (ETDEWEB)

    Balasubramanian, K; Zhao, C

    2004-03-17

    The ground and several excited states of metal aromatic clusters, namely NaM4 and NaM{sub 4}{sup {+-}} (M=Al, Ga, In) clusters have been investigated by employing complete activespace self-consistent-field (CASSCF) followed by Multi-reference singles and doubles configuration interaction (MRSDCI) computations that included up to 10 million configurations and other methods. The ground states NaM{sub 4}{sup -} of aromatic anions are found to be symmetric C{sub 4v} ({sup 1}A{sub 1}) electronic states with ideal square pyramid geometries. While the ground state of NaIn4 is also predicted to be a symmetric C{sub 4v} ({sup 2}A{sub 1}) square pyramid, the ground state of the NaAl4 cluster is found to have a C{sub 2v} ({sup 2}A{sub 1}) pyramid with a rhombus base and the ground state of NaGa{sub 4} possesses a C{sub 2v} ({sup 2}A{sub 1}) pyramid with a rectangle base. In general these structures exhibit 2 competing geometries, viz., an ideal C{sub 4v} structure and a distorted rhomboidal or rectangular pyramid structure (C{sub 2v}). All of the ground states of the NaM{sub 4}{sup +} (M= Al, Ga, In) cations are computed to be C{sub 2v} ({sup 3}A{sub 2}) pyramids with rhombus bases. The equilibrium geometries, vibrational frequencies, dissociation energies, adiabatic ionization potentials, adiabatic electron affinities for the electronic states of NaM{sub 4} (M=Al, Ga, In) and their ions are computed and compared with experimental results and other theoretical calculations. On the basis of our computed excited states energy separations, we have tentatively suggested assignments to the observed X and A states in the anion photoelectron spectra of Al{sub 4}Na{sup -} reported by Li et al. The X state can be assigned to a C{sub 2v} ({sup 2}A{sub 1}) rhomboidal pyramid. The A state observed in the anion spectrum is assigned to the first excited state ({sup 2}B{sub 1}) of the neutral NaAl{sub 4} with the C{sub 4v} symmetry. The assignments of the excited states are consistent with

  7. A phosphorescent silver(I)-gold (I) cluster complex that specifically lights up the nucleolus of living cells with FLIM imaging.

    Science.gov (United States)

    Chen, Min; Lei, Zhen; Feng, Wei; Li, Chunyan; Wang, Quan-Ming; Li, Fuyou

    2013-06-01

    The phosphorescent silver(I)-gold(I) cluster complex [CAu6Ag2(dppy)6](BF4)4 (N1) selectively stains the nucleolus, with a much lower uptake in the nucleus and cytoplasm, and exhibits excellent photostability. This Ag-Au cluster, which has a photoluminescent lifetime of microseconds, is particularly attractive as a probe in applications of time-gated microscopy. Investigation of the pathway of cellular entry indicated that N1 permeates the outer membrane and nuclear membrane of living cells through an energy-dependent and non-endocytic route within 10 min. High concentrations of N1 in the nucleolus have been quantified by inductively coupled plasma atomic emission spectroscopy (ICP-AES) and transmission electron microscopy coupled with an energy dispersive X-ray analysis (TEM-EDXA), which also helped to elucidate the mechanism of the specific staining. Intracellular selective staining may be correlated with the microenvironment of the nucleolus, which is consistent with experiments conducted at different phases of the cell cycle. These results prove that N1 is a very attractive phosphorescent staining reagent for visualizing the nucleolus of living cells.

  8. Clustering

    Directory of Open Access Journals (Sweden)

    Jinfei Liu

    2013-04-01

    Full Text Available DBSCAN is a well-known density-based clustering algorithm which offers advantages for finding clusters of arbitrary shapes compared to partitioning and hierarchical clustering methods. However, there are few papers studying the DBSCAN algorithm under the privacy preserving distributed data mining model, in which the data is distributed between two or more parties, and the parties cooperate to obtain the clustering results without revealing the data at the individual parties. In this paper, we address the problem of two-party privacy preserving DBSCAN clustering. We first propose two protocols for privacy preserving DBSCAN clustering over horizontally and vertically partitioned data respectively and then extend them to arbitrarily partitioned data. We also provide performance analysis and privacy proof of our solution..

  9. Formation of small vacancy clusters in tungsten around silver and indium impurities studied by PAC and THDS

    Energy Technology Data Exchange (ETDEWEB)

    Post, K.; Pleiter, F.; Hosson, J.Th.M. de (Rijksuniversiteit Groningen (Netherlands)); Kolk, G.J. van der; Veen, A. van; Caspers, L.M. (Interuniversitair Reactor Inst., Delft (Netherlands))

    1983-12-01

    Vacancy clustering at Ag and In impurities in W was investigated combining Thermal Helium Desorption Spectrometry (THDS) and Perturbed Angular Correlation (PAC) measurements. The results of these experiments are compared with each other and with those obtained from Monte Carlo calculations.

  10. Dynamics and fragmentation of van der Waals and hydrogen bonded cluster cations: (NH3)n and (NH3BH3)n ionized at 10.51 eV.

    Science.gov (United States)

    Yuan, Bing; Shin, Joong-Won; Bernstein, Elliot R

    2016-04-14

    A 118 nm laser is employed as a high energy, single photon (10.51 eV/photon) source for study of the dynamics and fragmentation of the ammonia borane (NH3BH3) cation and its cluster ions through time of flight mass spectrometry. The behavior of ammonia ion and its cluster ions is also investigated under identical conditions in order to explicate the ammonia borane results. Charge distributions, molecular orbitals, and spin densities for (NH3BH3)n and its cations are explored at both the second-order perturbation theory (MP2) and complete active space self-consistent field (CASSCF) theory levels. Initial dissociation mechanisms and potential energy surfaces for ionized NH3BH3, NH3, and their clusters are calculated at the MP2/6-311++G(d,p) level. Protonated clusters (NH3)xH(+) dominate ammonia cluster mass spectra: our calculations show that formation of (NH3)n-1H(+) and NH2 from the nascent (NH3)n(+) has the lowest energy barrier for the system. The only common features for the (NH3)n(+) and (NH3BH3)n(+) mass spectra under these conditions are found to be NHy(+) (y = 0,…,4) at m/z = 14-18. Molecular ions with both (11)B and (10)B isotopes are observed, and therefore, product ions observed for the (NH3BH3)n cluster system derive from (NH3BH3)n clusters themselves, not from the NH3 moiety of NH3BH3 alone. NH3BH2(+) is the most abundant ionization product in the (NH3BH3)n(+) cluster spectra: calculations support that for NH3BH3(+), an H atom is lost from the BH3 moiety with an energy barrier of 0.67 eV. For (NH3BH3)2(+) and (NH3BH3)3(+) clusters, a B(δ+)⋯H(δ-)⋯(δ-)H⋯(δ+)B bond can form in the respective cluster ions, generating a lower energy, more stable ion structure. The first step in the (NH3BH3)n(+) (n = 2, 3) dissociation is the breaking of the B(δ+)⋯H(δ-)⋯(δ-)H⋯(δ+)B moiety, leading to the subsequent release of H2 from the latter cluster ion. The overall reaction mechanisms calculated are best represented and understood employing a CASSCF

  11. Pb isotope geochemistry of lead, zinc, gold and silver deposit clustered region, Liaodong rift zone,northeastern China

    Institute of Scientific and Technical Information of China (English)

    CHEN; Jiangfeng; YU; Gang; XUE; Chunji; QIAN; Hui; HE; Jian

    2005-01-01

    33 Pb isotopic analyses were reported for sulfide and hydrothermal carbonate minerals and marble of the Xiquegou lead-zinc, the Zhenzigou zinc-lead and the Gaojiapuzi silver deposits from the Qingchengzi ore field and the Beiwagou zinc-lead deposit in the west, Proterozoic Liaodong rift zone. Pb isotopic ratios of the marble from the Qingchengzi ore field range from 18.24 to 30.63 for 206Pb/204Pb, 15.59 to 17.05 for 207Pb/204Pb and 37.43 to 38.63 for 208Pb/204Pb. The marble gives a Pb-Pb isochron age of 1822±92 Ma, which is interpreted as the age of the metamorphism of the marble. Ore Pb, including Pb of sulfide and hydrothermal carbonate minerals, from the Qingchengzi ore field shows limited variation with 206Pb/204Pb=17.66-17.96, 207Pb/204Pb=15.60-15.74 and 208Pb/204Pb=37.94-38.60. In contrast, ore Pb from the Beiwagou deposit gives different Pb isotopic ratios with 206Pb/204Pb=15.68-15.81, 207Pb/204Pb= 15.34-15.45 and 208Pb/204Pb=35.30-35.68. Pb of all deposits from the Liaodong rift zone is derived from the upper crust. Ore Pb of the Qingchengzi deposits is derived from a young upper crust. The model Th/U ratios of 4.40 to 4.74 for ore Pb are significantly different from that of 1.7 to 4.4 given by the marble of the Qingchengzi ore field, suggesting that marble is not the source of the ore Pb. Ore Pb of the Beiwagou deposit is extracted from its source and the deposit is formed at the Paleoproterozoic era. Different Pb isotopic ratios of the Qingchengzi ore field and the Beiwagou deposit are due to different ages of the deposits and suggest that the two types of deposits are derived from different sources and are possibly formed by different ore-forming processes.

  12. Cationic ruthenium alkylidene catalysts bearing phosphine ligands

    OpenAIRE

    Endo, Koji; Grubbs, Robert H.

    2016-01-01

    The discovery of highly active catalysts and the success of ionic liquid immobilized systems have accelerated attention to a new class of cationic metathesis catalysts. We herein report the facile syntheses of cationic ruthenium catalysts bear-ing bulky phosphine ligands. Simple ligand exchange using silver(I) salts of non-coordinating or weakly coordinating anions pro-vided either PPh3 or chelating Ph2P(CH2)nPPh2 (n = 2 or 3) ligated cationic catalysts. The structures of these newly reported...

  13. New Word Vector Representation for Semantic Clustering Une nouvelle représentation vectorielle pour la classification sémantique

    Directory of Open Access Journals (Sweden)

    Salma Jamoussi

    2010-09-01

    Full Text Available The idea we defend in this paper is the possibility to obtain significant semantic concepts using clustering methods. We start by defining some semantic measures to quantify the semantic relations between words. Then, we use some clustering methods to build up concepts in an automatic way. We test two well known methods: the K-means algorithm and the Ko- honen maps. Then, we propose the use of a Bayesian network conceived for clustering and called AutoClass. To group the words of the vocabulary in various classes, we test three vector representations of words. The first is a simple contextual representation. The second associates to each word a vector which represents its similarity with each word of the vocabulary. The third representation is a combination of the first and the second one.

  14. Silver Nanoparticles and Graphitic Carbon Through Thermal Decomposition of a Silver/Acetylenedicarboxylic Salt

    Directory of Open Access Journals (Sweden)

    Komninou Philomela

    2009-01-01

    Full Text Available Abstract Spherically shaped silver nanoparticles embedded in a carbon matrix were synthesized by thermal decomposition of a Ag(I/acetylenedicarboxylic acid salt. The silver nanoparticles, which are formed either by pyrolysis at 300 °C in an autoclave or thermolysis in xylene suspension at reflux temperature, are acting catalytically for the formation of graphite layers. Both reactions proceed through in situ reduction of the silver cations and polymerization of the central acetylene triple bonds and the exact temperature of the reaction can be monitored through DTA analysis. Interestingly, the thermal decomposition of this silver salt in xylene partly leads to a minor fraction of quasicrystalline silver, as established by HR-TEM analysis. The graphitic layers covering the silver nanoparticles are clearly seen in HR-TEM images and, furthermore, established by the presence of sp2carbon at the Raman spectrum of both samples.

  15. Separation of silver ions and starch modified silver nanoparticles using high performance liquid chromatography with ultraviolet and inductively coupled mass spectrometric detection

    Energy Technology Data Exchange (ETDEWEB)

    Hanley, Traci A.; Saadawi, Ryan; Zhang, Peng; Caruso, Joseph A., E-mail: joseph.caruso@uc.edu; Landero-Figueroa, Julio

    2014-10-01

    The production of commercially available products marketed to contain silver nanoparticles is rapidly increasing. Species-specific toxicity is a phenomenon associated with many elements, including silver, making it imperative to develop a method to identify and quantify the various forms of silver (namely, silver ions vs. silver nanoparticles) possibly present in these products. In this study a method was developed using high performance liquid chromatography (HPLC) with ultraviolet (UV–VIS) and inductively coupled mass spectrometric (ICP-MS) detection to separate starch stabilized silver nanoparticles (AgNPs) and silver ions (Ag{sup +}) by cation exchange chromatography with 0.5 M nitric acid mobile phase. The silver nanoparticles and ions were baseline resolved with an ICP-MS response linear over four orders of magnitude, 0.04 mg kg{sup −1} detection limit, and 90% chromatographic recovery for silver solutions containing ions and starch stabilized silver nanoparticles smaller than 100 nm.

  16. Simultaneous Interaction of Hydrophilic and Hydrophobic Solvents with Ethylamino Neurotransmitter Radical Cations: Infrared Spectra of Tryptamine(+)-(H2O)m-(N2)n Clusters (m,n ≤ 3).

    Science.gov (United States)

    Schütz, Markus; Sakota, Kenji; Moritz, Raphael; Schmies, Matthias; Ikeda, Takamasa; Sekiya, Hiroshi; Dopfer, Otto

    2015-10-01

    Solvation of biomolecules by a hydrophilic and hydrophobic environment strongly affects their structure and function. Here, the structural, vibrational, and energetic properties of size-selected clusters of the microhydrated tryptamine cation with N2 ligands, TRA(+)-(H2O)m-(N2)n (m,n ≤ 3), are characterized by infrared photodissociation spectroscopy in the 2800-3800 cm(-1) range and dispersion-corrected density functional theory calculations at the ωB97X-D/cc-pVTZ level to investigate the simultaneous solvation of this prototypical neurotransmitter by dipolar water and quadrupolar N2 ligands. In the global minimum structure of TRA(+)-H2O generated by electron ionization, H2O is strongly hydrogen-bonded (H-bonded) as proton acceptor to the acidic indolic NH group. In the TRA(+)-H2O-(N2)n clusters, the weakly bonded N2 ligands do not affect the H-bonding motif of TRA(+)-H2O and are preferentially H-bonded to the OH groups of the H2O ligand, whereas stacking to the aromatic π electron system of the pyrrole ring of TRA(+) is less favorable. The natural bond orbital analysis reveals that the H-bond between the N2 ligand and the OH group of H2O cooperatively strengthens the adjacent H-bond between the indolic NH group of TRA(+) and H2O, while π stacking is slightly noncooperative. In the larger TRA(+)-(H2O)m clusters, the H2O ligands form a H-bonded solvent network attached to the indolic NH proton, again stabilized by strong cooperative effects arising from the nearby positive charge. Comparison with the corresponding neutral TRA-(H2O)m clusters illustrates the strong impact of the excess positive charge on the structure of the microhydration network.

  17. Silver Sulfadiazine

    Science.gov (United States)

    ... degree burns. It kills a wide variety of bacteria.This medication is sometimes prescribed for other uses; ... or burned skin. Always wear a sterile, disposable glove when you apply silver sulfadiazine. Cover the cleaned ...

  18. Linear, branched and network polysilanes with thienyl/furyl substituted sila-alkyl side chains and their applications for the synthesis of fluorescent silver nanoparticles/clusters

    Indian Academy of Sciences (India)

    Ravi Shankar; Usharani Sahoo; Vandana Shahi; Manchal Chaudhary

    2012-11-01

    The scope of Wurtz coupling and catalytic dehydrocoupling methods for the synthesis of functional polysilanes of compositions, [RR'Si] (linear), [(PhMeSi)-co-(RSi)1−] (branched) and [RSi] (network) [R = Et3SiCH2CH2, 2-Fu/2-ThMe2SiCH2CH2 (Fu = Furyl, Th = Thienyl), -Hex or Ph; R' = H or Me] is presented. By virtue of -delocalized silicon backbone and variable HOMO-LUMO band gap energies, these polymers are found to be promising candidates as reducing agents for Ag(I) ions in toluene/cyclo-hexane and provide a simple approach for ‘size-controlled’ synthesis of silver nanoparticles (AgNPs) as well as fluorescent polymer-silver nanocomposites.

  19. Carnosine induced formation of silver nanochains: A radiolytic study

    Science.gov (United States)

    Malkar, Vishwabharati V.; Mukherjee, Tulsi; Kapoor, Sudhir

    2015-02-01

    Interaction of carnosine with silver clusters and its nanoparticles is studied at pH 8.2 and 9.2. Using time resolved kinetic measurements we show that carnosine interacts with the charged silver clusters. Using ionizing radiation silver particles are also produced in aqueous solution. In the presence of carnosine distinct differences in the surface plasmon absorption band of Ag nanoparticles is observed with change in pH. The results suggest that silver nanochains get formed through dipole-dipole interaction due to weak interaction with carnosine. UV-Vis spectrophotometry and transmission electron microscopy are used to characterize the nanoparticles.

  20. Photodissociation of Cerium Oxide Nanocluster Cations.

    Science.gov (United States)

    Akin, S T; Ard, S G; Dye, B E; Schaefer, H F; Duncan, M A

    2016-04-21

    Cerium oxide cluster cations, CexOy(+), are produced via laser vaporization in a pulsed nozzle source and detected with time-of-flight mass spectrometry. The mass spectrum displays a strongly preferred oxide stoichiometry for each cluster with a specific number of metal atoms x, with x ≤ y. Specifically, the most prominent clusters correspond to the formula CeO(CeO2)n(+). The cluster cations are mass selected and photodissociated with a Nd:YAG laser at either 532 or 355 nm. The prominent clusters dissociate to produce smaller species also having a similar CeO(CeO2)n(+) formula, always with apparent leaving groups of (CeO2). The production of CeO(CeO2)n(+) from the dissociation of many cluster sizes establishes the relative stability of these clusters. Furthermore, the consistent loss of neutral CeO2 shows that the smallest neutral clusters adopt the same oxidation state (IV) as the most common form of bulk cerium oxide. Clusters with higher oxygen content than the CeO(CeO2)n(+) masses are present with much lower abundance. These species dissociate by the loss of O2, leaving surviving clusters with the CeO(CeO2)n(+) formula. Density functional theory calculations on these clusters suggest structures composed of stable CeO(CeO2)n(+) cores with excess oxygen bound to the surface as a superoxide unit (O2(-)). PMID:27035210

  1. INTERACTION OF SILVER MOLECULAR CLUSTERS, INTRODUCED BY LOW-TEMPERATURE ION EXCHANGE METHOD, WITH NANOPARTICLES OF CdS IN FLUORINE PHOSPHATE GLASSES

    Directory of Open Access Journals (Sweden)

    N. D. Grazhdanov

    2015-09-01

    Full Text Available Glasses with metallic and semi-conductive nano-particles appear to be perspective non-linear and luminescent materials of photonics. It was shown in theory that composite optical materials containing semi-conductive CdS-core with Ag shell (or vice versa are optimal for enhancement of non-linear Kerr effect. Interaction of such an ensemble of particles leads to the forming of Ag island structures on the CdS particle, and formation of acanthite Ag2S on the two phases border (CdS-Ag is minimal. In glasses synthesis of CdS quantum dots occurred due to thermal treatment close to glass transition temperature; introduction of silver was realized by low-temperature ion exchange (LIE. The main object of this work is investigation of Ag+ -LIE effect on the growth of CdS nano-particles. Two glasses were explored in this work: without CdS (glass 1 and with CdS (glass 2, processed by LIE at the temperature of 320°С for 10, 20 and 30 minutes and subsequent heat treatment at temperatures of 410°С and 420°С. In case of glass 1, intensive luminescence appears as a result of LIE, and subsequent heat treatment results in surface resonance at λ=410 nm. In case of glass 2, absorbance spectra change appears that is specific for formation of acanthite and weak luminescence shifting to long-wavelength region (from 550 to 700 nm as a result of applying LIE and heat treatment. It indicates the growth of CdS quantum dots. Experiment has shown that quantum efficiency increases to 70% for glass 2 containing CdS quantum dots without LIE, while glass that contains silver shows steep decrease of quantum efficiency to 0%. That decrease is caused by formation of acanthite Ag2S on the surface of CdS quantum dot.

  2. Thermally induced morphological transition of silver fractals

    DEFF Research Database (Denmark)

    Solov'yov, Ilia; Solov'yov, Andrey; Kébaili, Nouari;

    2014-01-01

    We present both experimental and theoretical study of thermally induced morphological transition of silver nanofractals. Experimentally, those nanofractals formed from deposition and diffusion of preformed silver clusters on cleaved graphite surfaces exhibit dendritic morphologies that are highly...... sensitive to any perturbation, particularly caused by temperature. We analyze and characterize the morphological transition both in time and temperature using the recently developed Monte Carlo simulation approach for the description of nanofractal dynamics and compare the obtained results...

  3. Synthesis of hollow silver spheres using poly-(styrene-methyl acrylic acid) as templates in the presence of sodium polyacrylate

    Science.gov (United States)

    Wang, Aili; Yin, Hengbo; Ge, Chen; Ren, Min; Liu, Yumin; Jiang, Tingshun

    2010-02-01

    Hollow silver spheres were successfully prepared by reducing AgNO 3 with ascorbic acid and using negatively charged poly-(styrene-methyl acrylic acid) (PSA) spheres as templates in the presence of sodium polyacrylate as a stabilizer. Firstly, silver cations adsorbed on the surface of PSA spheres via electrostatic attraction between the carboxyl groups and silver cations were reduced in situ by ascorbic acid. The silver nanoparticles deposited on the surface of PSA spheres served as seeds for the further growth of silver shells. After that, extra amount of AgNO 3 and ascorbic acid solutions were added to form PSA/Ag composites with thick silver shells. In order to obtain compact silver shells, the as-prepared PSA/Ag composites were heated at 150 °C for 3 h. Then hollow silver spheres were prepared by dissolving PSA templates with tetrahydrofuran.

  4. Superatomic S(2) silver clusters stabilized by a thiolate-phosphine monolayer: insight into electronic and optical properties of Ag14(SC6H3F2)12(PPh3)8 and Ag16(SC6H3F2)14(DPPE)4.

    Science.gov (United States)

    Gell, Lars; Lehtovaara, Lauri; Häkkinen, Hannu

    2014-09-18

    The electronic structure of two recently crystallographically solved, thiolate-phosphine protected silver clusters Ag14 and Ag16 are analyzed via density functional theory (DFT) and their optical excitations are analyzed from time-dependent DFT perturbation theory. Both clusters can be characterized as having the S(2) free-electron configuration in the metal core, which is the first time such a configuration is confirmed for structurally known ligand-protected noble metal clusters. However, their different core shapes and ligand layer induce significantly different optical spectra. Performance of gradient-corrected DFT functionals is discussed and it is shown that the asymptotically correct Leeuwen-Baerends LB94 functional reproduces the optical spectrum of Ag14 in a good agreement with experiment. Choice of the functional becomes important for clusters where the optical transitions are dominated by the electron-rich ligand layer.

  5. First principles molecular dynamics simulation of a task-specific ionic liquid based on silver-olefin complex: atomistic insight into separation process

    CERN Document Server

    Jiang, De-en

    2008-01-01

    First principles molecular dynamics based on density functional theory is applied to a hypothetical ionic liquid whose cations and anions are silver-ethylene complex [Ag(C2H4)2+] and tetrafluoroborate [BF4-], respectively. This ionic liquid represents a group of task-specific silver complex-based ionic liquids synthesized recently. Molecular dynamics simulations at two temperatures are performed for five picoseconds. Events of association, dissociation, exchange, and recombination of ethylene with silver cation are observed. A mechanism of ethylene transfer similar to the Grotthus type of proton transfer in water is identified, where a silver cation accepts one ethylene molecule and donates another to a neighboring silver cation. This mechanism may contribute to fast transport of olefins through ionic liquid membranes based on silver complexes for olefin/paraffin separation.

  6. First principles molecular dynamics simulation of a task-specific ionic liquid based on silver-olefin complex: atomistic insights into a separation process.

    Science.gov (United States)

    Jiang, De-en; Dai, Sheng

    2008-08-21

    First principles molecular dynamics based on density functional theory is applied to a hypothetical ionic liquid whose cations and anions are silver-ethylene complex [Ag(C2H4)2+] and tetrafluoroborate [BF4-], respectively. This ionic liquid represents a group of task-specific silver complex-based ionic liquids synthesized recently. Molecular dynamics simulations at two temperatures are performed for five picoseconds. Events of association, dissociation, exchange, and recombination of ethylene with silver cation are found. A mechanism of ethylene transfer similar to the Grotthus type of proton transfer in water is identified, where a silver cation accepts one ethylene molecule and donates another to a neighboring silver cation. This mechanism may contribute to fast transport of olefins through ionic liquid membranes based on silver complexes for olefin/paraffin separation.

  7. An environmentally benign antimicrobial nanoparticle based on a silver-infused lignin core

    Science.gov (United States)

    Silver nanoparticles have antibacterial properties but their use has been a cause for concern because they persist in the environment. Here we show that lignin nanoparticles infused with silver ions and coated with a cationic polyelectrolyte layer form a biodegradable and green a...

  8. An environmentally benign antimicrobial nanoparticle based on a silver-infused lignin core

    NARCIS (Netherlands)

    Richter, Andries; Brown, J.S.; Bharti, B.; Wang, A.; Gangwal, S.; Houck, K.; Cohen Hubal, E.A.; Paunov, V.N.; Stoyanov, S.D.; Velev, O.D.

    2015-01-01

    Silver nanoparticles have antibacterial properties, but their use has been a cause for concern because they persist in the environment. Here, we show that lignin nanoparticles infused with silver ions and coated with a cationic polyelectrolyte layer form a biodegradable and green alternative to silv

  9. Fluorescence Microscopy of Nanoscale Silver Oxide Thin Films

    Institute of Scientific and Technical Information of China (English)

    PAN Xin-Yu; JIANG Hong-Bing; LIU Chun-Ling; GONG Qi-Huang; ZHANG Xi-Yao; ZHANG Qi-Feng; XU Bei-Xue; WU Jin-Lei

    2003-01-01

    The experimental conditions for photoactivated intermittent fluorescence from nanoscale silver oxide were studied with fluorescence microscopy. Strong fluorescence was observed from the Ag?O particles with size of 10-20nm excited with both blue and green light. We observed the saturation of photoexcitation with blue light and explained the experimental results using the model of agglomeration of silver atoms to form small clusters and the fluorescence of Ag2 and Ags clusters.

  10. Novel types of tetra-, hexa-, octa-, and dodecanuclear silver clusters containing (2,7-Di-tert-butylfluoren-9-ylidene)methanedithiolate.

    Science.gov (United States)

    Vicente, José; González-Herrero, Pablo; García-Sánchez, Yolanda; Jones, Peter G

    2009-03-01

    The reaction of AgClO(4) with piperidinium 2,7-di-tert-butyl-9H-fluorene-9-carbodithioate (pipH)[S(2)C(t-Bu-Hfy)] (1) (t-Bu-Hfy = 2,7-di-tert-butylfluoren-9-yl) afforded [Ag(n){S(2)C(t-Bu-Hfy)}(n)] (2), which reacted with phosphines to give [Ag{S(2)C(t-Bu-Hfy)}L(2)] [L = PPh(3) (3a); L(2) = bis(diphenylphosphino)ethane (dppe, 3b), 1,1'-bis(diphenylphosphino)ferrocene (dppf, 3c). By reacting complex 2 with AgClO(4) and piperidine in a 1:1:1 molar ratio, the dodecanuclear cluster [Ag(12){S(2)C(t-Bu-fy)}(6)] (4) (t-Bu-fy = 2,7-di-tert-butylfluoren-9-ylidene) was obtained. Compound 4 can also be directly prepared from the reaction of 1 with AgClO(4) and piperidine in a 1:2:1 molar ratio. The reactions of 1 with AgClO(4), phosphines, and piperidine afforded the compounds [Ag(6){S(2)C(t-Bu-fy)}(3)L(5)] [1:2:2:1 molar ratio; L = PPh(3) (5a), P(p-To)(3) (5b)], [Ag(4){S(2)C(t-Bu-fy)}(2)(dppf)(2)] (6) (1:2:1:1 molar ratio), [Ag(n){S(2)C(t-Bu-fy)}(n/2){P(i-Pr)(3)}(n)] (7) (1:2:2:1 molar ratio), or [Ag(8){S(2)C(t-Bu-fy)}(4){P(i-Pr)(3)}(4)] (8) (1:2:1:1 molar ratio). Complexes 5a,b, 6, 7, and 8 can be also obtained by reacting 4 with the corresponding phosphine in the appropriate molar ratio. The crystal structures of 4, 5b, and 8 have been determined by X-ray diffraction studies. The nuclearity of complex 6 was established from its (31)P{(1)H} NMR data, which reveal a very fast dynamic process leading to an average coupling of each of the P atoms of the dppf ligands with four Ag atoms. PMID:19235967

  11. Host–guest properties of the trinuclear arene–ruthenium cluster cation [H3Ru3(C6H6)(C6Me6)2(O)]+

    OpenAIRE

    Therrien, Bruno; Vieille-Petit, Ludovic; Süss-Fink, Georg

    2009-01-01

    The trinuclear arene–ruthenium cluster cation [H3Ru3(C6H6)(C6Me6)2(O)]+, containing a μ3-oxo cap and three arene ligands that span a hydrophobic pocket above the metal skeleton, has been crystallised as tetrafluoroborate salt in the presence of various guest molecules. The host–guest complexes have been characterised by single-crystal X-ray structure analysis. With chloroform as the guest molecule, a CHCl3 molecule sits perfectly in the hydrophobic pocket, the hydrogen atom being encapsulated...

  12. The Silver Halides

    Science.gov (United States)

    Sahyun, M. R. V.

    1977-01-01

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

  13. Ground state of naphthyl cation: Singlet or triplet?

    Energy Technology Data Exchange (ETDEWEB)

    Dutta, Achintya Kumar; Vaval, Nayana, E-mail: np.vaval@ncl.res.in; Pal, Sourav, E-mail: s.pal@ncl.res.in [Physical Chemistry Division, CSIR-National Chemical Laboratory, Pune 411008 (India); Manohar, Prashant U. [Department of Chemistry, BITS Pilani, Pilani Campus (India)

    2014-03-21

    We present a benchmark theoretical investigation on the electronic structure and singlet-triplet(S-T) gap of 1- and 2-naphthyl cations using the CCSD(T) method. Our calculations reveal that the ground states of both the naphthyl cations are singlet, contrary to the results obtained by DFT/B3LYP calculations reported in previous theoretical studies. However, the triplet states obtained in the two structural isomers of naphthyl cation are completely different. The triplet state in 1-naphthyl cation is (π,σ) type, whereas in 2-naphthyl cation it is (σ,σ{sup ′}) type. The S-T gaps in naphthyl cations and the relative stability ordering of the singlet and the triplet states are highly sensitive to the basis-set quality as well as level of correlation, and demand for inclusion of perturbative triples in the coupled-cluster ansatz.

  14. Extraordinarily high conductivity of flexible adhesive films by hybrids of silver nanoparticle–nanowires

    Science.gov (United States)

    Muhammed Ajmal, C.; Mol Menamparambath, Mini; Ryeol Choi, Hyouk; Baik, Seunghyun

    2016-06-01

    Highly conductive flexible adhesive (CFA) film was developed using micro-sized silver flakes (primary fillers), hybrids of silver nanoparticle–nanowires (secondary fillers) and nitrile butadiene rubber. The hybrids of silver nanoparticle–nanowires were synthesized by decorating silver nanowires with silver nanoparticle clusters using bifunctional cysteamine as a linker. The dispersion in ethanol was excellent for several months. Silver nanowires constructed electrical networks between the micro-scale silver flakes. The low-temperature surface sintering of silver nanoparticles enabled effective joining of silver nanowires to silver flakes. The hybrids of silver nanoparticle–nanowires provided a greater maximum conductivity (54 390 S cm‑1) than pure silver nanowires, pure multiwalled carbon nanotubes, and multiwalled carbon nanotubes decorated with silver nanoparticles in nitrile butadiene rubber matrix. The resistance change was smallest upon bending when the hybrids of silver nanoparticle–nanowires were employed. The adhesion of the film on polyethylene terephthalate substrate was excellent. Light emitting diodes were successfully wired to the CFA circuit patterned by the screen printing method for application demonstration.

  15. A Blue Photoluminescent Coordination Polymer Based on In Situ Generated Silver(Ⅰ) Cubane-like Clusters%含类立方烷银(Ⅰ)簇的光致蓝光配位聚合物的原位溶剂热合成

    Institute of Scientific and Technical Information of China (English)

    严冰; 吴涛; 李贞; 李丹

    2006-01-01

    A blue photoluminescent coordination polymer [Ag4Cl4(dppe)2]n has been prepared solvothermally and characterized structurally. The crystal structure was determined by single-crystal X-ray diffraction. The crystal is of tetragonal,space group I41/a,a=b=1.936 03(6) nm,c=1.465 63(8) nm,V=5.493 5(4) nm3,Z=4,Dcalcd=1.657 Mg·m-3, μ=1.749 mm-1. Reflections collected: 17 147, independent reflections: 3 247, Rint=0.021 1. Final R indices [I > 2σ(I)]: R1=0.044 8, wR2=0.111 0. The structure of [Ag4Cl4(dppe)2]n is a 3D-diamond highly symmetrical polymeric network containing Ag4Cl4 cubane-like clusters connected by 1,2-bis(diphenylphosphino)ethane (dppe). Each Ag4C14 cluster is composed of four silver and four chlorine atoms situated at alternate vertexes of a highly distorted cube with each silver atom being further coordinated to one phosphorus atom from a dppe ligand. The stripping of chloride ions from CHCl3 provides the source for chlorine in the formation of Ag(Ⅰ) clusters. In addition,the emission spectrum of the complex 1 in solid state has been studied. CCDC: 288080.

  16. Activity of Antimicrobial Silver Polystyrene Nanocomposites

    Directory of Open Access Journals (Sweden)

    M. Palomba

    2012-01-01

    Full Text Available A simple technique based on doping polymers with in situ generated silver nanoparticles (Ag/PS films has been developed. In particular, an antiseptic material has been prepared by dissolving silver 1,5-cyclooctadiene-hexafluoroacetylacetonate in amorphous polystyrene, and the obtained solid solution has been heated for ca. 10 s at a convenient temperature (180°C. Under such conditions the metal precursor decomposes producing silver atoms that diffuse into the polymer and clusterize. The antimicrobial characteristics of the resulting polystyrene-based material have been accurately evaluated toward Escherichia coli (E. coli comparing the cytotoxicity effect of 10 wt.% and 30 wt.% (drastic and mild annealing silver-doped polystyrene to the corresponding pure micrometric silver powder. Two different bacterial viability assays were performed in order to demonstrate the cytotoxic effect of Ag/PS films on cultured E. coli: (1 turbidimetric determination of optical density; (2 BacLight fluorescence-based test. Both methods have shown that silver-doped polystyrene (30 wt.% provides higher antibacterial activity than pure Ag powder, under similar concentration and incubation conditions.

  17. The reduction process of phytic acid silver ion system: A pulse radiolysis study

    Science.gov (United States)

    Joshi, Ravi; Mukherjee, Tulsi

    2007-05-01

    Reduction of silver ion in a silver-phytic acid (1:1 ratio) system has been studied using pulse radiolysis technique. Time-resolved transformation of the intermediates, Ag +→Ag 0→Ag 2+→Ag 32+, has been clearly observed in the reduction of silver-phytic acid (1:1) system. The effect of phytic acid on the formation and decay of initial silver clusters has been also studied. The surface plasmon absorption band of stable silver nanoparticle (410 nm) and dynamic light scattering technique has been used to characterize the nanoparticles and measure the average size ( Rav=100 nm).

  18. The reduction process of phytic acid-silver ion system: A pulse radiolysis study

    International Nuclear Information System (INIS)

    Reduction of silver ion in a silver-phytic acid (1:1 ratio) system has been studied using pulse radiolysis technique. Time-resolved transformation of the intermediates, Ag+→Ag0→Ag2+→Ag32+, has been clearly observed in the reduction of silver-phytic acid (1:1) system. The effect of phytic acid on the formation and decay of initial silver clusters has been also studied. The surface plasmon absorption band of stable silver nanoparticle (410 nm) and dynamic light scattering technique has been used to characterize the nanoparticles and measure the average size (R av=100 nm)

  19. Polystyrene Based Silver Selective Electrodes

    Directory of Open Access Journals (Sweden)

    Shiva Agarwal

    2002-06-01

    Full Text Available Silver(I selective sensors have been fabricated from polystyrene matrix membranes containing macrocycle, Me6(14 diene.2HClO4 as ionophore. Best performance was exhibited by the membrane having a composition macrocycle : Polystyrene in the ratio 15:1. This membrane worked well over a wide concentration range 5.0×10-6–1.0×10-1M of Ag+ with a near-Nernstian slope of 53.0 ± 1.0 mV per decade of Ag+ activity. The response time of the sensor is <15 s and the membrane can be used over a period of four months with good reproducibility. The proposed electrode works well in a wide pH range 2.5-9.0 and demonstrates good discriminating power over a number of mono-, di-, and trivalent cations. The sensor has also been used as an indicator electrode in the potentiometric titration of silver(II ions against NaCl solution. The sensor can also be used in non-aqueous medium with no significant change in the value of slope or working concentration range for the estimation of Ag+ in solution having up to 25% (v/v nonaqueous fraction.

  20. Femtosecond laser structuring of silver-containing glass: Silver redistribution, selective etching, and surface topology engineering

    Energy Technology Data Exchange (ETDEWEB)

    Desmoulin, Jean-Charles; Petit, Yannick; Cardinal, Thierry, E-mail: thierry.cardinal@icmcb.cnrs.fr [CNRS, ICMCB, UPR 9048, F-33600 Pessac, France and Univ. Bordeaux, ICMCB, UPR 9048, F-33600 Pessac (France); Canioni, Lionel [Université Bordeaux, Centre Lasers Intenses et Applications–UMR 5107 CNRS, 351 cours de la Libération, 33405 Talence Cedex (France); Dussauze, Marc [Université de Bordeaux, Institut des Sciences Moléculaires, CNRS UMR 5255, 351 cours de la Libération, 33405 Talence Cedex (France); Lahaye, Michel [Université de Bordeaux, Placamat, avenue Docteur Albert Schweitzer, 33608 Pessac Cedex (France); Gonzalez, Hernando Magallanes; Brasselet, Etienne [Université Bordeaux, Laboratoire Ondes et Matière d' Aquitaine–UMR 5798, CNRS, 351 cours de la Libération, 33405 Talence Cedex (France)

    2015-12-07

    Femtosecond direct laser writing in silver-containing phosphate glasses allows for the three-dimensional (3D) implementation of complex photonic structures. Sample translation along or perpendicular to the direction of the beam propagation has been performed, which led to the permanent formation of fluorescent structures, either corresponding to a tubular shape or to two parallel planes at the vicinity of the interaction voxel, respectively. These optical features are related to significant modifications of the local material chemistry. Indeed, silver depletion areas with a diameter below 200 nm were evidenced at the center of the photo-produced structures while photo-produced luminescence properties are attributed to the formation of silver clusters around the multiphoton interaction voxel. The laser-triggered oxidation-reduction processes and the associated photo-induced silver redistribution are proposed to be at the origin of the observed original 3D luminescent structures. Thanks to such material structuring, surface engineering has been also demonstrated. Selective surface chemical etching of the glass has been obtained subsequently to laser writing at the location of the photo-produced structures, revealing features with nanometric depth profiles and radial dimensions strongly related to the spatial distributions of the silver clusters.

  1. Adsorption of silver dimer on graphene - A DFT study

    Energy Technology Data Exchange (ETDEWEB)

    Kaur, Gagandeep, E-mail: gaganj1981@yahoo.com [Department of Physics and Centre of Advanced Studies in Physics, Panjab University, Chandigarh-160014, India and Chandigarh Engineering College, Landran, Mohali-140307, Punjab (India); Gupta, Shuchi [Department of Physics and Centre of Advanced Studies in Physics, Panjab University, Chandigarh-160014, India and University Institute of Engineering and Technology, Panjab University, Chandigarh -160014 (India); Rani, Pooja; Dharamvir, Keya [Department of Physics and Centre of Advanced Studies in Physics, Panjab University, Chandigarh-160014 (India)

    2014-04-24

    We performed a systematic density functional theory (DFT) study of the adsorption of silver dimer (Ag{sub 2}) on graphene using SIESTA (Spanish Initiative for Electronic Simulations with Thousands of Atoms) package, in the generalized gradient approximation (GGA). The adsorption energy, geometry, and charge transfer of Ag2-graphene system are calculated. The minimum energy configuration for a silver dimer is parallel to the graphene sheet with its two atoms directly above the centre of carbon-carbon bond. The negligible charge transfer between the dimer and the surface is also indicative of a weak bond. The methodology demonstrated in this paper may be applied to larger silver clusters on graphene sheet.

  2. Unexpected Ultrafast Silver Ion Reduction: Dynamics Driven by the Solvent Structure.

    Science.gov (United States)

    Balcerzyk, Anna; Schmidhammer, Uli; Horne, Gregory; Wang, Furong; Ma, Jun; Pimblott, Simon M; de la Lande, Aurélien; Mostafavi, Mehran

    2015-08-01

    Picosecond pulse radiolysis measurements have been performed in neutral and highly acidic aqueous solutions containing silver ions at different concentrations. Silver ion reduction is used to understand the ultrafast chemistry of irradiated water and aqueous solutions. The absorption band measured at the end of the 7-ps electron pulses has an intense band with a maximum at 360 nm due to the formation of silver atoms. Kinetics shows that the amount of silver atom formed at the end of the electron pulse in phosphoric acid solutions is greater than that in neutral water. This unexpectedly high yield of silver atom formation cannot be explained solely by the reaction between silver ions and solvated electrons in neutral solutions nor by the reaction with hydrogen atoms in phosphoric acid solutions. To explain the observed ultrafast reduction of silver ions, the presolvated electron, be it free or paired to the hydronium cation, must react very quickly with a silver ion, potentially competing with geminate recombination of the electron and its sibling radical cation. PMID:26158320

  3. Electronic Origins of the Variable Efficiency of Room-Temperature Methane Activation by Homo- and Heteronuclear Cluster Oxide Cations [XYO2](+) (X, Y = Al, Si, Mg): Competition between Proton-Coupled Electron Transfer and Hydrogen-Atom Transfer.

    Science.gov (United States)

    Li, Jilai; Zhou, Shaodong; Zhang, Jun; Schlangen, Maria; Weiske, Thomas; Usharani, Dandamudi; Shaik, Sason; Schwarz, Helmut

    2016-06-29

    The reactivity of the homo- and heteronuclear oxide clusters [XYO2](+) (X, Y = Al, Si, Mg) toward methane was studied using Fourier transform ion cyclotron resonance mass spectrometry, in conjunction with high-level quantum mechanical calculations. The most reactive cluster by both experiment and theory is [Al2O2](•+). In its favorable pathway, this cluster abstracts a hydrogen atom by means of proton-coupled electron transfer (PCET) instead of following the conventional hydrogen-atom transfer (HAT) route. This mechanistic choice originates in the strong Lewis acidity of the aluminum site of [Al2O2](•+), which cleaves the C-H bond heterolytically to form an Al-CH3 entity, while the proton is transferred to the bridging oxygen atom of the cluster ion. In addition, a comparison of the reactivity of heteronuclear and homonuclear oxide clusters [XYO2](+) (X, Y = Al, Si, Mg) reveals a striking doping effect by aluminum. Thus, the vacant s-p hybrid orbital on Al acts as an acceptor of the electron pair from methyl anion (CH3(-)) and is therefore eminently important for bringing about thermal methane activation by PCET. For the Al-doped cluster ions, the spin density at an oxygen atom, which is crucial for the HAT mechanism, acts here as a spectator during the course of the PCET mediated C-H bond cleavage. A diagnostic plot of the deformation energy vis-à-vis the barrier shows the different HAT/PCET reactivity map for the entire series. This is a strong connection to the recently discussed mechanism of oxidative coupling of methane on magnesium oxide surfaces proceeding through Grignard-type intermediates.

  4. Copper and silver halates

    CERN Document Server

    Woolley, EM; Salomon, M

    2013-01-01

    Copper and Silver Halates is the third in a series of four volumes on inorganic metal halates. This volume presents critical evaluations and compilations for halate solubilities of the Group II metals. The solubility data included in this volume are those for the five compounds, copper chlorate and iodate, and silver chlorate, bromate and iodate.

  5. Adduct formation of ionic and nanoparticular silver with amino acids and glutathione

    Energy Technology Data Exchange (ETDEWEB)

    Blaske, Franziska; Stork, Lisa; Sperling, Michael; Karst, Uwe, E-mail: uk@uni-muenster.de [University of Muenster, Institute of Inorganic and Analytical Chemistry (Germany)

    2013-09-15

    To investigate the interaction of ionic and nanoparticular silver with amino acids and small peptides, an electrospray ionization time-of-flight mass spectrometry method was developed. Monomeric and oligomeric silver adducts were formed with amino acids including cysteine (Cys), methionine, histidine, lysine, or the tripeptide glutathione (GSH). The obtained spectra for ionic silver show clusters in different ratios between Ag{sup +} and the reaction partners (X) including [Ag{sub n}X{sub m} - (n + 1)H]{sup -} (n = 1-4, m = 1-3). Regarding Cys, adduct clusters up to n = 5 and m = 4 were observed as well. Considering silver-GSH interactions, even doubly charged oligomers occur generating [Ag{sub (a+1)}GSH{sub a} - (a + 3)H]{sup 2-} (a = 5-7) and [Ag{sub b}GSH{sub b} - (b + 2)H]{sup 2-} (b = 4-8) ions. {sup 1}H NMR data of free GSH compared to that after treatment with Ag{sup +} confirm sulfur-metal interactions due to changing chemical shifts for the protons located adjacent to the thiol group. Density functional theory calculations for silver-GSH clusters may explain the formation of experimentally recorded large clusters due to cooperative effects between silver and carboxylic acid side chains. Both sets of experiments indicate the presence of these adducts in the liquid phase. For silver nanoparticles, the respective data confirm the release of silver ions and the subsequent adduct formation.

  6. Evaluation of Silver Distribution within the Silver Doped Hydroxyapatite

    OpenAIRE

    Dubņika, A; Loča, D; Jakovļevs, D; Bērziņa-Cimdiņa, L.

    2013-01-01

    Various researches of silver doped hydroxyapatite (HAp/Ag) synthesis and evaluation can be found, but scarce information can be found on evaluation of silver distribution within powders and pallets depending on the material preparation method. Silver distribution is essential parameter responsible for silver release and material in vitro properties.

  7. Room-temperature silver-containing liquid metal salts with nitrate anions

    OpenAIRE

    Schaltin, Stijn; Brooks, Neil R.; Sniekers, Jeroen; Depuydt, Daphne; Van Meervelt, Luc; Binnemans, Koen; Fransaer, Jan

    2013-01-01

    The synthesis, structural, thermal and electrochemical properties of fluorine-free silver-containing ionic liquids are presented. The ionic liquid cations are formed by a silver(I) ion surrounded by two 1-alkylimidazole ligands, with the counter anions being nitrate ions. Depending on the alkyl chain length, the complexes were found to be liquids at room temperature or melting slightly above this. For the solid compounds it was possible to elucidate the structure by single crystal X-ray analy...

  8. Nanosecond (ns) laser transfer of silver nanoparticles from silver-exchanged soda-lime glass to transparent soda-lime glass and shock waves formation

    Science.gov (United States)

    Sow, Mohamed Chérif; Blondeau, Jean-Philippe; Sagot, Nadine; Ollier, Nadège; Tite, Teddy

    2015-05-01

    In this contribution, we showed for the first time in our knowledge a single-step process for silver clusters and nanoparticles growth and transfer from silver-exchanged soda-lime glass to un-exchanged soda-lime glass (transparent glass in visible and NIR domain) by nanosecond (ns) laser irradiation. The transferred silver nanoparticles in transparent glass are strongly linked to the glass surface. In addition, we point out the formation of shock waves, with selective silver clustering on the top wave. This technique provides an alternative and simple way to obtain metallic nanoparticles in different media which can be traversed by laser wavelength used. Moreover, this experiment is made at room temperature and air environment. It is worth noting that our technique requires a glass previously doped with the corresponding silver ions.

  9. Mineral commodity profiles: Silver

    Science.gov (United States)

    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. Selective Facet Reactivity During Cation Exchange in Cadmium Sulfide Nanorods

    Energy Technology Data Exchange (ETDEWEB)

    Sadtler, Bryce; Demchenko, Denis; Zheng, Haimei; Hughes, Steven; Merkle, Maxwell; Dahmen, Ulrich; Wang, Lin-Wang; Alivisatos, A. Paul

    2008-12-18

    The partial transformation of ionic nanocrystals through cation exchange has been used to synthesize nanocrystal heterostructures. We demonstrate that the selectivity for cation exchange to take place at different facets of the nanocrystal plays an important role in determining the resulting morphology of the binary heterostructure. In the case of copper I (Cu+) cation exchange in cadmium sulfide (CdS) nanorods, the reaction starts preferentially at the ends of the nanorods such that copper sulfide (Cu2S) grows inwards from either end. The resulting morphology is very different from the striped pattern obtained in our previous studies of silver I (Ag+) exchange in CdS nanorods where non-selective nucleation of silver sulfide (Ag2S) occurs. From interface formation energies calculated for several models of epitaxialconnections between CdS and Cu2S or Ag2S, we infer the relative stability of each interface during the nucleation and growth of Cu2S or Ag2S within the CdS nanorods. The epitaxial connections of Cu2S to the end facets of CdS nanorods minimize the formation energy, making these interfaces stable throughout the exchange reaction. However, as the two end facets of wurtzite CdS nanorods are crystallographically nonequivalent, asymmetric heterostructures can be produced.

  11. Synthesis and characterization of magnetite/silver/antibiotic nanocomposites for targeted antimicrobial therapy.

    Science.gov (United States)

    Ivashchenko, Olena; Lewandowski, Mikołaj; Peplińska, Barbara; Jarek, Marcin; Nowaczyk, Grzegorz; Wiesner, Maciej; Załęski, Karol; Babutina, Tetyana; Warowicka, Alicja; Jurga, Stefan

    2015-10-01

    The article is devoted to preparation and characterization of magnetite/silver/antibiotic nanocomposites for targeted antimicrobial therapy. Magnetite nanopowder was produced by thermochemical technique; silver was deposited on the magnetite nanoparticles in the form of silver clusters. Magnetite/silver nanocomposite was investigated by XRD, SEM, TEM, AFM, XPS, EDX techniques. Adsorptivity of magnetite/silver nanocomposite towards seven antibiotics from five different groups was investigated. It was shown that rifampicin, doxycycline, ceftriaxone, cefotaxime and doxycycline may be attached by physical adsorption to magnetite/silver nanocomposite. Electrostatic surfaces of antibiotics were modeled and possible mechanism of antibiotic attachment is considered in this article. Raman spectra of magnetite, magnetite/silver and magnetite/silver/antibiotic were collected. It was found that it is difficult to detect the bands related to antibiotics in the magnetite/silver/antibiotic nanocomposite spectra due to their overlap by the broad carbon bands of magnetite nanopowder. Magnetic measurements revealed that magnetic saturation of the magnetite/silver/antibiotic nanocomposites decreased on 6-19 % in comparison with initial magnetite nanopowder. Pilot study of antimicrobial properties of the magnetite/silver/antibiotic nanocomposites were performed towards Bacillus pumilus.

  12. Quasielastic neutron scattering study of silver selenium halides

    CERN Document Server

    Major, A G; Barnes, A C; Howells, W S

    2002-01-01

    Both silver chalcogenides (Ag sub 2 S, Ag sub 2 Se, and Ag sub 2 Te) and silver halides (AgCl, AgBr, and AgI) are known to be fast-ion solids in which the silver ions can diffuse quickly in a sublattice formed by the other ions. To clarify whether mixtures of these materials (such as Ag sub 3 SeI) possess comparable properties and whether a systematic dependence on the cation-to-anion ratio can be observed, some of these mixtures were studied by quasielastic neutron scattering both in the solid and the liquid phases. To identify the diffusion mechanisms and constants, a new data-analysis method based on a two-dimensional maximum-likelihood fit is proposed. This method has the potential to give more reliable information on the diffusion mechanism than the traditional Bayesian method. (orig.)

  13. High current density electrodeposition of silver from silver-containing liquid metal salts with pyridine-N-oxide ligands.

    Science.gov (United States)

    Sniekers, Jeroen; Brooks, Neil R; Schaltin, Stijn; Van Meervelt, Luc; Fransaer, Jan; Binnemans, Koen

    2014-01-28

    New cationic silver-containing ionic liquids were synthesized and used as non-aqueous electrolytes for the electrodeposition of silver layers. In the liquid state of these ionic liquids, a silver (i) cation is coordinated by pyridine-N-oxide (py-O) ligands in a 1 : 3 metal-to-ligand ratio, although in some cases a different stoichiometry of the silver center crystallized out. As anions, bis(trifluoromethanesulfonyl)imide (Tf2N), trifluoromethanesulfonate (OTf), methanesulfonate (OMs) and nitrate were used, yielding compounds with the formulae [Ag(py-O)3][Tf2N], [Ag(py-O)3][OTf], [Ag(py-O)3][OMs] and [Ag(py-O)3][NO3], respectively. The compounds were characterized by CHN analysis, FTIR, NMR, DSC, TGA and the electrodeposition of silver was investigated by cyclic voltammetry, linear potential scans, scanning electron microscopy (SEM) and energy-dispersive X-ray spectrometry (EDX). With the exception of [Ag(py-O)3][Tf2N], which melts at 108 °C, all the silver(i) compounds have a melting point below 80 °C and were tested as electrolytes for silver electrodeposition. Interestingly, very high current densities were observed at a potential of -0.5 V vs. Ag/Ag(+) for the compounds with fluorine-free anions, i.e. [Ag(py-O)3][NO3] (current density of -10 A dm(-2)) and [Ag(py-O)3][OMs] (-6.5 A dm(-2)). The maximum current density of the compound with the fluorinated anion trifluoromethanesulfonate, [Ag(py-O)3][OTf], was much lower: -2.5 A dm(-2) at -0.5 V vs. Ag/Ag(+). Addition of an excess of ligand to [Ag(py-O)3][OTf] resulted in the formation of the room-temperature ionic liquid [Ag(py-O)6][OTf]. A current density of -5 A dm(-2) was observed at -0.5 V vs. Ag/Ag(+) for this low viscous silver salt. The crystal structures of several silver complexes could be determined by X-ray diffraction, and it was found that several of them had a stoichiometry different from the 1 : 3 metal-to-ligand ratio used in their synthesis. This indicates that the compounds form crystals

  14. PIXE analysis of medieval silver coins

    International Nuclear Information System (INIS)

    We applied the proton-induced X-ray emission (PIXE) analytical technique to twenty-eight medieval silver coins, selected from the Tunisian treasury. The purpose is to study the fineness evolution from the beginning of the 7th to the 15th centuries AD. Each silver coin was cleaned with a diluted acid solution and then exposed to a 3 MeV proton beam from a 1.7 MV tandem accelerator. To allow the simultaneous detection of light and heavy elements, a funny aluminum filter was positioned in front of the Si(Li) detector entrance which is placed at 135o to the beam direction. The elements Cu, Pb, and Au were observed in the studied coins along with the major component silver. The concentration of Ag, presumably the main constituent of the coins, varies from 55% to 99%. This significant variation in the concentration of the major constituent reveals the economical difficulties encountered by each dynasty. It could be also attributed to differences in the composition of the silver mines used to strike the coins in different locations. That fineness evolution also reflects the poor quality of the control practices during this medieval period. In order to verify the ability of PIXE analytical method to distinguish between apparently similar coins, we applied hierarchical cluster analysis to our results to classify them into different subgroups of similar elemental composition.

  15. Study of chemical processes involved in silver staining of gold nanostructures by Raman scattering

    Science.gov (United States)

    Ji, Xiaohui; Yang, Wensheng

    2016-05-01

    Strong Raman enhancement contributed by ``hot spots'' in directly fused gold dimers offer a selective and sensitive tool for understanding the surface processes involved in the silver staining of gold nanostructures. These processes include the interactions of cations, effects of surface adsorbed Cl- ions, surface replacement of ligands, and reduction of silver ions on the surface of the gold nanocrystals. Results show that in the commonly applied silver staining scheme for gold nanostructures, i.e., the addition of the Raman probe after the deposition of the silver shell, the Raman signals of the probe (p-mercaptobenzoic acid) were weakened greatly, due to the pre-existence of the Cl--Ag+-citrate bridges on the surface of the gold. A new scheme was developed for silver deposition after pre-adsorption of the probe, which achieved a Raman enhancement factor as high as ~5 × 108.Strong Raman enhancement contributed by ``hot spots'' in directly fused gold dimers offer a selective and sensitive tool for understanding the surface processes involved in the silver staining of gold nanostructures. These processes include the interactions of cations, effects of surface adsorbed Cl- ions, surface replacement of ligands, and reduction of silver ions on the surface of the gold nanocrystals. Results show that in the commonly applied silver staining scheme for gold nanostructures, i.e., the addition of the Raman probe after the deposition of the silver shell, the Raman signals of the probe (p-mercaptobenzoic acid) were weakened greatly, due to the pre-existence of the Cl--Ag+-citrate bridges on the surface of the gold. A new scheme was developed for silver deposition after pre-adsorption of the probe, which achieved a Raman enhancement factor as high as ~5 × 108. Electronic supplementary information (ESI) available: Fig. S1-S3. See DOI: 10.1039/c6nr01208f

  16. Silver enhancement of nanogold and undecagold

    Energy Technology Data Exchange (ETDEWEB)

    Hainfield, J.F.; Furuya, F.R.

    1995-07-01

    A recent advance in immunogold technology has been the use of molecular gold instead of colloidal gold. A number of advantages are realized by this approach, such as stable covalent, site-specific attachment, small probe size and absence of aggregates for improved penetration. Silver enhancement has led to improved and unique results for electron and light microscopy, as well as their use with blots and gels. Most previous work with immunogold silver staining has been done with colloidal gold particles. More recently, large gold compounds (``clusters``) having a definite number of gold atoms and defined organic shell, have been used, frequently with improved results. These gold dusters, large compared to simple compounds, are, however, at the small end of the colloidal gold scale in size; undecagold is 0.8 nm and Nanogold is 1.4 nm. They may be used in practically all applications where colloidal gold is used (Light and electron microscopy, dot blots, etc.) and in some unique applications, where at least the larger colloidal golds don`t work, such as running gold labeled proteins on gels (which are later detected by silver enhancement). The main differences between gold clusters and colloidal golds are the small size of the dusters and their covalent attachment to antibodies or other molecules.

  17. Laser-Cluster-Interaction in a Nanoplasma-Model with Inclusion of Lowered Ionization Energies

    OpenAIRE

    Hilse, Paul; Moll, Max; Schlanges, Manfred; Bornath, Thomas

    2008-01-01

    The interaction of intense laser fields with silver and argon clusters is investigated theoretically using a modified nanoplasma model. Single pulse and double pulse excitations are considered. The influence of the dense cluster environment on the inner ionization processes is studied including the lowering of the ionization energies. There are considerable changes in the dynamics of the laser-cluster interaction. Especially, for silver clusters, the lowering of the ionization energies leads ...

  18. Probing the Intact Cluster Catalysis Concept by Tetrahedral Clusters With Framework Chirality

    Institute of Scientific and Technical Information of China (English)

    G. Süss-Fink; L. Vieille-Petit

    2005-01-01

    @@ 1Results and Discussion In order to bring evidence for or against the hypothesis of catalytic hydrogenation by intact trinuclear arene ruthenium clusters containing an oxo cap, the substrate being hydrogenated inside the hydrophobic pocket spanned by the three arene ligands ("supramolecular cluster catalysis")[1], we synthesized cationic Ru3O clusters (See Fig. 1) with three different arene ligands (intrinsically chiral tetrahedra).

  19. Nanosecond (ns) laser transfer of silver nanoparticles from silver-exchanged soda-lime glass to transparent soda-lime glass and shock waves formation

    International Nuclear Information System (INIS)

    Highlights: • Silver nanoparticles growth by nanosecond laser irradiation of silver exchanged soda-lime glasses. • Silver nanoparticles transfer. • Nanosecond laser induced shock waves formation on glass. - Abstract: In this contribution, we showed for the first time in our knowledge a single-step process for silver clusters and nanoparticles growth and transfer from silver-exchanged soda-lime glass to un-exchanged soda-lime glass (transparent glass in visible and NIR domain) by nanosecond (ns) laser irradiation. The transferred silver nanoparticles in transparent glass are strongly linked to the glass surface. In addition, we point out the formation of shock waves, with selective silver clustering on the top wave. This technique provides an alternative and simple way to obtain metallic nanoparticles in different media which can be traversed by laser wavelength used. Moreover, this experiment is made at room temperature and air environment. It is worth noting that our technique requires a glass previously doped with the corresponding silver ions

  20. Nanosecond (ns) laser transfer of silver nanoparticles from silver-exchanged soda-lime glass to transparent soda-lime glass and shock waves formation

    Energy Technology Data Exchange (ETDEWEB)

    Sow, Mohamed Chérif, E-mail: mohamed-cherif.sow@univ-orleans.fr [Laboratoire CEMTHI UPR CNRS 3079, Université d’Orléans, IUT de Chartres, 28000 Chartres (France); Blondeau, Jean-Philippe; Sagot, Nadine [Laboratoire CEMTHI UPR CNRS 3079, Université d’Orléans, IUT de Chartres, 28000 Chartres (France); Ollier, Nadège; Tite, Teddy [Laboratoire Hubert Curien UMR CNRS 5516, Université de Lyon, Université Jean Monnet, 42000 Saint-Etienne (France)

    2015-05-01

    Highlights: • Silver nanoparticles growth by nanosecond laser irradiation of silver exchanged soda-lime glasses. • Silver nanoparticles transfer. • Nanosecond laser induced shock waves formation on glass. - Abstract: In this contribution, we showed for the first time in our knowledge a single-step process for silver clusters and nanoparticles growth and transfer from silver-exchanged soda-lime glass to un-exchanged soda-lime glass (transparent glass in visible and NIR domain) by nanosecond (ns) laser irradiation. The transferred silver nanoparticles in transparent glass are strongly linked to the glass surface. In addition, we point out the formation of shock waves, with selective silver clustering on the top wave. This technique provides an alternative and simple way to obtain metallic nanoparticles in different media which can be traversed by laser wavelength used. Moreover, this experiment is made at room temperature and air environment. It is worth noting that our technique requires a glass previously doped with the corresponding silver ions.

  1. New Guar Biopolymer Silver Nanocomposites for Wound Healing Applications

    Directory of Open Access Journals (Sweden)

    Runa Ghosh Auddy

    2013-01-01

    Full Text Available Wound healing is an innate physiological response that helps restore cellular and anatomic continuity of a tissue. Selective biodegradable and biocompatible polymer materials have provided useful scaffolds for wound healing and assisted cellular messaging. In the present study, guar gum, a polymeric galactomannan, was intrinsically modified to a new cationic biopolymer guar gum alkylamine (GGAA for wound healing applications. Biologically synthesized silver nanoparticles (Agnp were further impregnated in GGAA for extended evaluations in punch wound models in rodents. SEM studies showed silver nanoparticles well dispersed in the new guar matrix with a particle size of ~18 nm. In wound healing experiments, faster healing and improved cosmetic appearance were observed in the new nanobiomaterial treated group compared to commercially available silver alginate cream. The total protein, DNA, and hydroxyproline contents of the wound tissues were also significantly higher in the treated group as compared with the silver alginate cream (P<0.05. Silver nanoparticles exerted positive effects because of their antimicrobial properties. The nanobiomaterial was observed to promote wound closure by inducing proliferation and migration of the keratinocytes at the wound site. The derivatized guar gum matrix additionally provided a hydrated surface necessary for cell proliferation.

  2. Silver ion release from antimicrobial polyamide/silver composites

    OpenAIRE

    Kumar, Radhesh; Münstedt, Helmut

    2005-01-01

    Silver ion (Ag+) the versatile antimicrobial species was released in a steady and prolonged manner from a silver-filled polyamide composite system. Metallic silver powder having varying specific surface area (SSA) has been used as a resource of biocide in polyamide. Strong evidences are found showing the release of the antimicrobial species from the resulting composite upon soaking it in water due to the interaction of the diffused water molecules with the dispersed silver powder wit...

  3. Small angle neutron scattering analysis of chitosan- silver nanocomposite films

    International Nuclear Information System (INIS)

    Recently biopolymers are extensively studied for the development of solid polymer electrolytes. Studies relating to interaction of nanoparticles with biopolymers are essential to furthering research in solid polymer electrolytes. In our research we have tried to understand the interaction between chitosan and silver nanoparticles during reduction process. Chitosan is linear polysaccharides obtained from the deacetylation of chitin. It is soluble in acidic medium and the D-glucosamine unit gets protonated leading to poly cationic polymer. It has wide potential applications in medical, water engineering, sensors, and in micro device fabrication due to its unique physiochemical properties including biocompatibility and non toxicity. It also acts as both reducing and stabilizing agent for the metal ions via ion pair interaction. Silver nanoparticles are used as filler due to its well-known effectiveness in biomedical, electronic, catalytic and optical applications. In this research we have synthesized chitosan - silver films. The films were synthesized by solution casting method and polymer films of thickness ~ 100 μm were obtained. The chitosan - silver films were also dipped in hydrazine hydrate for comparison. Various characterizations techniques such as XRD, FTIR, SEM, TEM and SANS were used. SEM and TEM showed structural modifications in the chitosan- silver film which is enhanced when dipped in hydrazine hydrate. Interestingly, Small angle neutron scattering (SANS) showed that fractals were formed in the chitosan- silver films both dipped and undipped in hydrazine hydrate. Electrical characterization studies showed that the conductivity was affected due to formation of silver nanoparticles. These films have potential application in solid batteries.

  4. Silver selective electrodes based on thioether functionalized calix[4]arenes as ionophores

    NARCIS (Netherlands)

    Malinowska, Elz˙bieta; Brzozka, Zbigniew; Kasiura, Krzysztof; Egberink, Richard J.M.; Reinhoudt, David N.

    1994-01-01

    Silver selective electrodes based on thioether functionalized calix[4]arenes 1 and 2 as ionophores were investigated. For both ionophores the selectivity coefficients (log kAg,M) were lower than −2.2 for Hg(II) and lower than −4.6 for other cations tested. The best results were obtained with membran

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

    Science.gov (United States)

    Hauri, James F.; Niece, Brian K.

    2011-01-01

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

  6. Lysozyme-coated silver nanoparticles for differentiating bacterial strains on the basis of antibacterial activity

    Science.gov (United States)

    Ashraf, Sumaira; Chatha, Mariyam Asghar; Ejaz, Wardah; Janjua, Hussnain Ahmed; Hussain, Irshad

    2014-10-01

    Lysozyme, an antibacterial enzyme, was used as a stabilizing ligand for the synthesis of fairly uniform silver nanoparticles adopting various strategies. The synthesized particles were characterized using UV-visible spectroscopy, FTIR, dynamic light scattering (DLS), and TEM to observe their morphology and surface chemistry. The silver nanoparticles were evaluated for their antimicrobial activity against several bacterial species and various bacterial strains within the same species. The cationic silver nanoparticles were found to be more effective against Pseudomonas aeruginosa 3 compared to other bacterial species/strains investigated. Some of the bacterial strains of the same species showed variable antibacterial activity. The difference in antimicrobial activity of these particles has led to the conclusion that antimicrobial products formed from silver nanoparticles may not be equally effective against all the bacteria. This difference in the antibacterial activity of silver nanoparticles for different bacterial strains from the same species may be due to the genome islands that are acquired through horizontal gene transfer (HGT). These genome islands are expected to possess some genes that may encode enzymes to resist the antimicrobial activity of silver nanoparticles. These silver nanoparticles may thus also be used to differentiate some bacterial strains within the same species due to variable silver resistance of these variants, which may not possible by simple biochemical tests.

  7. An environmentally benign antimicrobial nanoparticle based on a silver-infused lignin core

    Science.gov (United States)

    Richter, Alexander P.; Brown, Joseph S.; Bharti, Bhuvnesh; Wang, Amy; Gangwal, Sumit; Houck, Keith; Cohen Hubal, Elaine A.; Paunov, Vesselin N.; Stoyanov, Simeon D.; Velev, Orlin D.

    2015-09-01

    Silver nanoparticles have antibacterial properties, but their use has been a cause for concern because they persist in the environment. Here, we show that lignin nanoparticles infused with silver ions and coated with a cationic polyelectrolyte layer form a biodegradable and green alternative to silver nanoparticles. The polyelectrolyte layer promotes the adhesion of the particles to bacterial cell membranes and, together with silver ions, can kill a broad spectrum of bacteria, including Escherichia coli, Pseudomonas aeruginosa and quaternary-amine-resistant Ralstonia sp. Ion depletion studies have shown that the bioactivity of these nanoparticles is time-limited because of the desorption of silver ions. High-throughput bioactivity screening did not reveal increased toxicity of the particles when compared to an equivalent mass of metallic silver nanoparticles or silver nitrate solution. Our results demonstrate that the application of green chemistry principles may allow the synthesis of nanoparticles with biodegradable cores that have higher antimicrobial activity and smaller environmental impact than metallic silver nanoparticles.

  8. Spectroscopic, microscopic and catalytic properties of silver nanoparticles synthesized using Saraca indica flower

    Science.gov (United States)

    Vidhu, V. K.; Philip, Daizy

    2014-01-01

    The bioprospective field is dynamic area of research in the recent years. The present article reports a green synthetic route for the production of highly stable, bio-inspired silver nanoparticles using dried Saraca indica flower. The method is facile, cost effective, simple and reproducible. The reduction of silver ions and the formation of silver nanoparticles has been monitored using UV-visible spectroscopy. The TEM, SAED and XRD result reveal that the silver nanoparticles are crystalline in nature. FTIR spectra are used to identify the biomolecules that bind on the surface of silver nanoparticles, which increased the stability of the particles. S. indica flower extract plays its role as an excellent reducing agent of silver ions and the biosynthesized silver nanoparticles are safer to environment. Also the size dependent catalytic activity of silver nanoparticles in the reduction of cationic dye, Methylene blue by NaBH4 is studied by UV-visible spectroscopy. The efficiency of synthesized nanoparticles as an excellent catalyst is proved by the reduction of Methylene blue which is confirmed by the decrease in the absorbance with time and is attributed to electron relay effect.

  9. Theoretical Investigation on the Adsorption of Ag+ and Hydrated Ag+ Cations on Clean Si(111)Surface

    Institute of Scientific and Technical Information of China (English)

    SHENG Yong-Li; LI Meng-Hua; WANG Zhi-Guo; LIU Yong-Jun

    2008-01-01

    In this paper,the adsorption of Ag+ and hydrated Ag+ cations on clean Si(111)surface were investigated by using cluster(Gaussian 03)and periodic(DMol3)ab initio calculations.Si(111)surface was described with cluster models(Si14H17 and Si22H21)and a four-silicon layer slab with periodic boundary conditions.The effect of basis set superposition error(BSSE)was taken into account by applying the counterpoise correction.The calculated results indicated that the binding energies between hydrated Ag+ cations and clean Si(111)surface are large,suggesting a strong interaction between hydrated Ag+ cations and the semiconductor surface.With the increase of number,water molecules form hydrogen bond network with one another and only one water molecule binds directly to the Ag+ cation.The Ag+ cation in aqueous solution will safely attach to the clean Si(111)surface.

  10. Stability and structure of nanowires grown from silver, copper and their alloys by laser ablation into superfluid helium.

    Science.gov (United States)

    Gordon, Eugene; Karabulin, Alexander; Matyushenko, Vladimir; Sizov, Vyacheslav; Khodos, Igor

    2014-12-14

    Nanowires with 5 nm diameter made of silver, copper, and their alloys were grown in superfluid helium. The silver nanowires being heated to 300 K disintegrated into individual clusters. In contrast, copper nanowires were stable at room temperature, and nanowires made of alloys were also stable despite their low melting temperature.

  11. Ion exchange behaviour of polymeric zirconium cations

    International Nuclear Information System (INIS)

    Polymeric zirconium cations formed in weakly acid solutions (pH2) are taken up strongly into macroporous cation exchange resins, while uptake into normal cation exchange resins (pore diameter about 1 nm) is low. Macroporous cation exchange resins loaded with polymeric Zr cations are shown to function as ligand exchange sorbents. (Authors)

  12. Potted Silver Carp

    Institute of Scientific and Technical Information of China (English)

    1998-01-01

    Ingredients: 4 silver carp of about 200 grams each, mushrooms, winter bamboo shoots, minced ginger root and scallions, cooking wine, broth, salt and MSG (optional). Method: 1. After cleaning the carp place them in a pot; add in all other ingredients and some broth, Seal the opening of the pot with kraft paper

  13. Silver Bear for Screenplay

    Institute of Scientific and Technical Information of China (English)

    LIU YUNYUN

    2010-01-01

    @@ Chinese director Wang Quan'an won the Silver Bear Prize at the 60th Berlin International Film Festival that lasted during February 11 to 21 tor the best screenplay for his movie Apart Together.The film also opened the festival.

  14. Two new polyoxovanadate clusters templated through cysteamine

    Indian Academy of Sciences (India)

    K Pavani; S Upreti; A Ramanan

    2006-03-01

    Two new fully oxidized polyoxovanadate cluster-based solids (C4N2S2H14)2[H2V10O28]$\\cdot$4H2O, 1 and (C4N2S2H14)5[H4V15O42]2.10H2O, 2 are crystallized under self-assembly process in the presence of cysteamine. In both 1 and 2, cysteamines are oxidized forming disulphide linkages and occur as counter cations. The organic cations assemble around V10O28 cluster anions in 1 whereas they aggregate around V15O42 clusters in 2. pH appears to be the structure determinant in the occurrence of decavanadate cluster in 1 and pentadecavanadate in 2, with the same counter cation.

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

    Energy Technology Data Exchange (ETDEWEB)

    Kvitek, L; Panacek, A; Prucek, R; Soukupova, J; Vanickova, M; Zboril, R [Regional Centre of Advanced Technologies and Materials, Department of Physical Chemistry, Faculty of Science, Palacky University, 17. Listopadu 12, 77146 Olomouc (Czech Republic); Kolar, M, E-mail: ales.panacek@upol.cz [Department of Microbiology, Faculty of Medicine and Dentistry, Palacky University, Hnevotinska 3, 77520 Olomouc (Czech Republic)

    2011-07-06

    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. The reduction process of phytic acid-silver ion system: A pulse radiolysis study

    Energy Technology Data Exchange (ETDEWEB)

    Joshi, Ravi [Radiation and Photochemistry Division, Chemistry Group, Bhabha Atomic Research Center, Mumbai 400 085 (India)]. E-mail: rjudrin@yahoo.com; Mukherjee, Tulsi [Radiation and Photochemistry Division, Chemistry Group, Bhabha Atomic Research Center, Mumbai 400 085 (India)

    2007-05-15

    Reduction of silver ion in a silver-phytic acid (1:1 ratio) system has been studied using pulse radiolysis technique. Time-resolved transformation of the intermediates, Ag{sup +{yields}}Ag{sup 0{yields}}Ag{sub 2} {sup +{yields}}Ag{sub 3} {sup 2+}, has been clearly observed in the reduction of silver-phytic acid (1:1) system. The effect of phytic acid on the formation and decay of initial silver clusters has been also studied. The surface plasmon absorption band of stable silver nanoparticle (410 nm) and dynamic light scattering technique has been used to characterize the nanoparticles and measure the average size (R {sub av}=100 nm)

  17. Molecular modeling of organic corrosion inhibitors: why bare metal cations are not appropriate models of oxidized metal surfaces and solvated metal cations.

    Science.gov (United States)

    Kokalj, Anton

    2014-01-01

    The applicability of various models of oxidized metal surfaces - bare metal cations, clusters of various size, and extended (periodic) slabs - that are used in the field of quantum-chemical modeling of corrosion inhibitors is examined and discussed. As representative model systems imidazole inhibitor, MgO surface, and solvated Mg(2+) ion are considered by means of density-functional-theory calculations. Although the results of cluster models are prone to cluster size and shape effects, the clusters of moderate size seem useful at least for qualitative purposes. In contrast, the bare metal cations are useless not only as models of oxidized surfaces but also as models of solvated cations, because they bind molecules several times stronger than the more appropriate models. In particular, bare Mg(2+) binds imidazole by 5.9 eV, while the slab model of MgO(001) by only 0.35 eV. Such binding is even stronger for 3+ cations, e.g., bare Al(3+) binds imidazole by 17.9 eV. The reasons for these fantastically strong binding energies are discussed and it is shown that the strong bonding is predominantly due to electron charge transfer from molecule to metal cation, which stems from differences between molecular and metal ionization potentials.

  18. Assessment of Size-Dependent Antimicrobial and Cytotoxic Properties of Silver Nanoparticles

    Directory of Open Access Journals (Sweden)

    Yoon Jeong

    2014-01-01

    Full Text Available Nanoscale silver has been increasingly applied to commercial products for their antimicrobial function as antibiotics and disinfectants. In this work, the different sizes of silver nanoparticles (AgNPs were studied not only in Methylobacterium spp. for their antimicrobial potential but also in human peripheral blood mononuclear cells (PBMCs for their cytotoxicity in order to determine responses dependent on their particle size. Size controlled silver particles were prepared by chemical reduction of silver cations (Ag+ and then dispersed in water for their physicochemical characterization using transmission electron microscopy (TEM, dynamic light scattering (DLS, and zeta potential measurements. To ascertain antimicrobial response, water-soluble silver nanoparticles were mixed into Methylobacterium spp. cultured for two days and the sample from the broth was spread on the agar plate for colony counting. 10 nm nanoparticles showed more antimicrobial activity than 100 nm particles at which concentrations were equivalently controlled. Increased cytotoxic effect of smaller silver nanoparticles was also observed in PBMCs cocultured with particles. Silver ions released from 10 nm particles might be correlated with upregulated antimicrobial and cytotoxic properties of AgNPs.

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

    Energy Technology Data Exchange (ETDEWEB)

    Sathaiyan, N.; Nandakumar, V.; Ramachandran, P. [Central Electrochemical Research Institute, Karaikudi 630 006 (India)

    2006-10-27

    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{sup o}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 -0.600V (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. (author)

  20. Liquid-solid extraction of cationic metals by cationic amphiphiles

    International Nuclear Information System (INIS)

    In the field of selective separation for recycling of spent nuclear fuel, liquid-liquid extraction processes are widely used (PUREX, DIAMEX..) in industrial scale. In order to guarantee a sustainable nuclear energy for the forthcoming generations, alternative reprocessing techniques are under development. One of them bases on the studies from Heckmann et al in the 80's and consists in selectively precipitating actinides from aqueous waste solutions by cationic surfactants (liquid-solid extraction). This technique has some interesting advantages over liquid-liquid extraction techniques, because several steps are omitted like stripping or solvent washing. Moreover, the amount of waste is decreased considerably, since no contaminated organic solvent is produced. In this thesis, we have carried out a physico-chemical study to understand the specific interactions between the metallic cations with the cationic surfactant. First, we have analysed the specific effect of the different counter-ions (Cl-, NO3-, C2O42-) and then the effect of alkaline cations on the structural properties of the surfactant aggregation in varying thermodynamical conditions. Finally, different multivalent cations (Cu2+, Zn2+, UO22+, Fe3+, Nd3+, Eu3+, Th4+) were considered; we have concluded that depending on the anionic complex of these metals formed in acidic media, we can observe either an adsorption at the micellar interface or not. This adsorption has a large influence of the surfactant aggregation properties and determines the limits of the application in term of ionic strength, temperature and surfactant concentration. (author)

  1. Efficacy of silver coated surgical sutures on bacterial contamination, cellular response and wound healing.

    Science.gov (United States)

    Gallo, Anna Lucia; Paladini, Federica; Romano, Alessandro; Verri, Tiziano; Quattrini, Angelo; Sannino, Alessandro; Pollini, Mauro

    2016-12-01

    The resistance demonstrated by many microorganisms towards conventional antibiotics has stimulated the interest in alternative antimicrobial agents and in novel approaches for prevention of infections. Silver, a natural braod-spectrum antimicrobial agent known since antiquity, has been widely employed in biomedical field due to its recognized antibacterial, antifungal and antiviral properties. In this work, antibacterial silver coatings were deposited on absorbable surgical sutures through the in situ photo-chemical deposition of silver clusters. Scanning electron microscopy (SEM), Energy dispersive X-ray spectroscopy (EDX) and thermo-gravimetric analysis (TGA) were performed in order to investigate the presence and distribution of the silver clusters on the substrate. The amounts of silver deposited and released by the silver treated sutures were calculated through Inductively Coupled Plasma-Mass Spectroscopy (ICP-MS), and the results were related to the biodegradation of the material. The microbiological properties and the potential cytotoxicity of the silver-treated sutures were investigated in relation with hydrolysis experiments, in order to determine the effect of the degradation on antibacterial properties and biocompatibility. PMID:27612783

  2. Silver against Pseudomonas aeruginosa biofilms

    DEFF Research Database (Denmark)

    Bjarnsholt, Thomas; Kirketerp-Møller, K.; Kristiansen, S.;

    2007-01-01

    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 ig/mL silver sulfadiazine eradicated the biofilm whereas a lower concentration (1 ig/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...

  3. Surface characterization of silver and palladium modified glassy carbon

    Indian Academy of Sciences (India)

    Aleksandra A Perić-Grujić; Olivera M Nešković; Miomir V Veljković; Zoran V Laušević; Mila D Laušević

    2007-12-01

    In this work, the influence of silver and palladium on the surface of undoped, boron doped and phosphorus doped glassy carbon has been studied. The silver and palladium concentrations in solution, after metal deposition, were measured by atomic absorption spectrophotometer. The morphology of metal coatings was characterized by scanning electron microscopy. In order to investigate the nature and thermal stability of surface oxygen groups, temperature-programmed desorption method combined with mass spectrometric analyses, was performed. The results obtained have shown that silver and palladium spontaneously deposit from their salt solutions at the surface of glassy carbon samples. Silver deposits have dendrite structure, whilst palladium forms separate clusters. The highest amount of both silver and palladium deposits at the surface of sample containing the highest quantity of surface oxide complexes. It has been concluded that carboxyl groups and structure defects are responsible for metal reduction. Calculated desorption energies have shown that the surface modification by metal deposition leads to the formation of more stable surface of undoped and doped glassy carbon samples.

  4. Synthesis, characterization, and in vivo efficacy of shell cross-linked nanoparticle formulations carrying silver antimicrobials as aerosolized therapeutics.

    Science.gov (United States)

    Shah, Parth N; Lin, Lily Yun; Smolen, Justin A; Tagaev, Jasur A; Gunsten, Sean P; Han, Daniel S; Heo, Gyu Seong; Li, Yali; Zhang, Fuwu; Zhang, Shiyi; Wright, Brian D; Panzner, Matthew J; Youngs, Wiley J; Brody, Steven L; Wooley, Karen L; Cannon, Carolyn L

    2013-06-25

    The use of nebulizable, nanoparticle-based antimicrobial delivery systems can improve efficacy and reduce toxicity for treatment of multi-drug-resistant bacteria in the chronically infected lungs of cystic fibrosis patients. Nanoparticle vehicles are particularly useful for applying broad-spectrum silver-based antimicrobials, for instance, to improve the residence time of small-molecule silver carbene complexes (SCCs) within the lung. Therefore, we have synthesized multifunctional, shell cross-linked knedel-like polymeric nanoparticles (SCK NPs) and capitalized on the ability to independently load the shell and core with silver-based antimicrobial agents. We formulated three silver-loaded variants of SCK NPs: shell-loaded with silver cations, core-loaded with SCC10, and combined loading of shell silver cations and core SCC10. All three formulations provided a sustained delivery of silver over the course of at least 2-4 days. The two SCK NP formulations with SCC10 loaded in the core each exhibited excellent antimicrobial activity and efficacy in vivo in a mouse model of Pseudomonas aeruginosa pneumonia. SCK NPs with shell silver cation-load only, while efficacious in vitro, failed to demonstrate efficacy in vivo. However, a single dose of core SCC10-loaded SCK NPs (0.74 ± 0.16 mg Ag) provided a 28% survival advantage over sham treatment, and administration of two doses (0.88 mg Ag) improved survival to 60%. In contrast, a total of 14.5 mg of Ag(+) delivered over 5 doses at 12 h intervals was necessary to achieve a 60% survival advantage with a free-drug (SCC1) formulation. Thus, SCK NPs show promise for clinical impact by greatly reducing antimicrobial dosage and dosing frequency, which could minimize toxicity and improve patient adherence. PMID:23718195

  5. Investigation of Silver Doped Hydroxyapatite

    OpenAIRE

    Dubņika, A; Loča, D; Mālniece, L

    2012-01-01

    Biomaterials based on calcium phosphate ceramics are used as implants in human/animal body due to their excellent biocompatibility. Silver containing materials have a very broad spectrum of antibacterial activity; therefore silver doped hydroxyapatite can be used in medicine as antibacterial implant material. The aim of this work was to synthesize monophasic and biphasic silver doped hydroxyapatite and evaluate the differences in their physical and antibacterial properties.

  6. Star-like superalkali cations featuring planar pentacoordinate carbon.

    Science.gov (United States)

    Guo, Jin-Chang; Tian, Wen-Juan; Wang, Ying-Jin; Zhao, Xue-Feng; Wu, Yan-Bo; Zhai, Hua-Jin; Li, Si-Dian

    2016-06-28

    Superalkali cations, known to possess low vertical electron affinities (VEAs), high vertical detachment energies, and large highest occupied molecular orbital (HOMO)-lowest unoccupied molecular orbital (LUMO) energy gaps, are intriguing chemical species. Thermodynamically, such species need to be the global minima in order to serve as the promising targets for experimental realization. In this work, we propose the strategies of polyhalogenation and polyalkalination for designing the superalkali cations. By applying these strategies, the local-minimum planar pentacoordinate carbon (ppC) cluster CBe5 can be modified to form a series of star-like superalkali ppC or quasi-ppC CBe5X5 (+) (X = F, Cl, Br, Li, Na, K) cations containing a CBe5 moiety. Polyhalogenation and polyalkalination on the CBe5 unit may help eliminate the high reactivity of bare CBe5 molecule by covering the reactive Be atoms with noble halogen anions and alkali cations. Computational exploration of the potential energy surfaces reveals that the star-like ppC or quasi-ppC CBe5X5 (+) (X = F, Cl, Br, Li, Na, K) clusters are the true global minima of the systems. The predicted VEAs for CBe5X5 (+) range from 3.01 to 3.71 eV for X = F, Cl, Br and 2.12-2.51 eV for X = Li, Na, K, being below the lower bound of the atomic ionization potential of 3.89 eV in the periodic table. Large HOMO-LUMO energy gaps are also revealed for the species: 10.76-11.07 eV for X = F, Cl, Br and 4.99-6.91 eV for X = Li, Na, K. These designer clusters represent the first series of superalkali cations with a ppC center. Bonding analyses show five Be-X-Be three-center two-electron (3c-2e) σ bonds for the peripheral bonding, whereas the central C atom is associated with one 6c-2e π bond and three 6c-2e σ bonds, rendering (π and σ) double aromaticity. Born-Oppenheimer molecular dynamics simulations indicate that the CBe5 motif is robust in the clusters. As planar hypercoordination carbon species are often thermodynamically

  7. Star-like superalkali cations featuring planar pentacoordinate carbon

    Science.gov (United States)

    Guo, Jin-Chang; Tian, Wen-Juan; Wang, Ying-Jin; Zhao, Xue-Feng; Wu, Yan-Bo; Zhai, Hua-Jin; Li, Si-Dian

    2016-06-01

    Superalkali cations, known to possess low vertical electron affinities (VEAs), high vertical detachment energies, and large highest occupied molecular orbital (HOMO)-lowest unoccupied molecular orbital (LUMO) energy gaps, are intriguing chemical species. Thermodynamically, such species need to be the global minima in order to serve as the promising targets for experimental realization. In this work, we propose the strategies of polyhalogenation and polyalkalination for designing the superalkali cations. By applying these strategies, the local-minimum planar pentacoordinate carbon (ppC) cluster CBe5 can be modified to form a series of star-like superalkali ppC or quasi-ppC CBe5X5+ (X = F, Cl, Br, Li, Na, K) cations containing a CBe5 moiety. Polyhalogenation and polyalkalination on the CBe5 unit may help eliminate the high reactivity of bare CBe5 molecule by covering the reactive Be atoms with noble halogen anions and alkali cations. Computational exploration of the potential energy surfaces reveals that the star-like ppC or quasi-ppC CBe5X5+ (X = F, Cl, Br, Li, Na, K) clusters are the true global minima of the systems. The predicted VEAs for CBe5X5+ range from 3.01 to 3.71 eV for X = F, Cl, Br and 2.12-2.51 eV for X = Li, Na, K, being below the lower bound of the atomic ionization potential of 3.89 eV in the periodic table. Large HOMO-LUMO energy gaps are also revealed for the species: 10.76-11.07 eV for X = F, Cl, Br and 4.99-6.91 eV for X = Li, Na, K. These designer clusters represent the first series of superalkali cations with a ppC center. Bonding analyses show five Be-X-Be three-center two-electron (3c-2e) σ bonds for the peripheral bonding, whereas the central C atom is associated with one 6c-2e π bond and three 6c-2e σ bonds, rendering (π and σ) double aromaticity. Born-Oppenheimer molecular dynamics simulations indicate that the CBe5 motif is robust in the clusters. As planar hypercoordination carbon species are often thermodynamically unstable and

  8. Cationic speciation in nonaqueous media

    International Nuclear Information System (INIS)

    Electronic spectra of solutions of d transition elements in the superacids HF, H2SO4, HSO3F, and CF3SO3H and in chloroaluminate melts indicate that in acidic monaqueous media the elements are present as solvated cations, whereas in basic media the speciation is anionic, the same situation as in aqueous solutions. Further, in very highly acidic media, cations in very low oxidation states are stable (e.g., Ti2+), but these disproportionate on addition of base to the system. In this paper spectra, where available, of U, Np, and Pu in oxidation states III and IV in aqueous media, in protonic superacids, and in chloroaluminates are presented to postulate cationic speciation of these early actinides in highly acidic media

  9. Ionic liquids of bis(alkylethylenediamine)silver(I) salts and the formation of silver(0) nanoparticles from the ionic liquid system.

    Science.gov (United States)

    Iida, Masayasu; Baba, Chihiro; Inoue, Michiko; Yoshida, Hibiki; Taguchi, Eiji; Furusho, Hirotoshi

    2008-01-01

    We have prepared novel ionic liquids of bis(N-2-ethylhexylethylenediamine)silver(I) nitrate ([Ag(eth-hex-en)(2)]NO(3) and bis(N-hexylethylenediamine)silver(I) hexafluorophosphate ([Ag(hex-en)(2)]PF(6)), which have transition points at -54 and -6 degrees C, respectively. Below these transition temperatures, both the silver complexes assume amorphous states, in which the extent of the vitrification is larger for the eth-hex-en complex than for the hex-en complex. The diffusion coefficients of both the complex cations, measured between 30 (or 35) and 70 degrees C, are largely dependent on temperature; the dependence is particularly large in the case of the eth-hex-en complex cation below 40 degrees C. Small-angle X-ray scattering studies showed that the bilayer structure of the metal complex is formed in the liquid state for both the silver complexes. A direct observation of the yellowish [Ag(eth-hex-en)(2)]NO(3) liquid by transmission electron microscopy (TEM) indicates the presence of nanostructures, as a microemulsion, of less than 5 nm. Such structures were not clearly observed in the [Ag(hex-en)(2)]PF(6) liquid. Although the [Ag(eth-hex-en)(2)]NO(3) liquid is sparingly soluble in bulk water, it readily incorporates a small amount of water up to [water]/[metal complex] = 7:1. Homogeneous and uniformly sized silver(0) nanoparticles in water were created by the reduction of the [Ag(eth-hex-en)(2)]NO(3) liquid with aqueous NaBH(4), whereas silver(0) nanoparticles were not formed from the [Ag(hex-en)(2)]PF(6) liquid in the same way. PMID:18399524

  10. Electron attachment and electron ionization of acetic acid clusters embedded in helium nanodroplets

    NARCIS (Netherlands)

    da Silva, F. Ferreira; Jaksch, S.; Martins, G.; Dang, H. M.; Dampc, M.; Denifl, S.; Maerk, T. D.; Limao-Vieira, P.; Liu, J.; Yang, S.; Ellis, A. M.; Scheier, P.

    2009-01-01

    The effect of incident electrons on acetic acid clusters is explored for the first time. The acetic acid clusters are formed inside liquid helium nanodroplets and both cationic and anionic products ejected into the gas phase are detected by mass spectrometry. The cation chemistry (induced by electro

  11. Corrosion protection for silver reflectors

    Energy Technology Data Exchange (ETDEWEB)

    Arendt, Paul N. (Los Alamos, NM); Scott, Marion L. (Los Alamos, NM)

    1991-12-31

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

  12. Weighted Clustering

    DEFF Research Database (Denmark)

    Ackerman, Margareta; Ben-David, Shai; Branzei, Simina;

    2012-01-01

    We investigate a natural generalization of the classical clustering problem, considering clustering tasks in which different instances may have different weights.We conduct the first extensive theoretical analysis on the influence of weighted data on standard clustering algorithms in both the...... partitional and hierarchical settings, characterizing the conditions under which algorithms react to weights. Extending a recent framework for clustering algorithm selection, we propose intuitive properties that would allow users to choose between clustering algorithms in the weighted setting and classify...

  13. Vacancies in silver

    International Nuclear Information System (INIS)

    Resistivity and positron lifetime measurements were performed to follow the annealing of the vacancy defects in quenched or irradiated high purity silver. For quench temperatures in the range 4000C to 5000C, the quenched-in resistivity is restored in one single stage centered at 400C. An activation energy of 0.64 +- 0.06 eV is inferred for the migration of the single vacancies. This result together with the information derived from the evolution of positron lifetime spectra leads to the conclusion that stage III is to be assigned to monovacancy migration. Further results obtained in α-AgZn solid solutions support this view. (author)

  14. Laser desorption/ionization mass spectrometry of lipids using etched silver substrates.

    Science.gov (United States)

    Schnapp, Andreas; Niehoff, Ann-Christin; Koch, Annika; Dreisewerd, Klaus

    2016-07-15

    Silver-assisted laser desorption/ionization mass spectrometry can be used for the analysis of small molecules. For example, adduct formation with silver cations enables the molecular analysis of long-chain hydrocarbons, which are difficult to ionize via conventional matrix-assisted laser desorption ionization (MALDI). Here we used highly porous silver foils, produced by etching with nitric acid, as sample substrates for LDI mass spectrometry. As model system for the analysis of complex lipid mixtures, cuticular extracts of fruit flies (Drosophila melanogaster) and worker bees (Apis mellifera) were investigated. The mass spectra obtained by spotting extract onto the etched silver substrates demonstrate the sensitive detection of numerous lipid classes such as long-chain saturated and unsaturated hydrocarbons, fatty acyl alcohols, wax esters, and triacylglycerols. MS imaging of cuticular surfaces with a lateral resolution of a few tens of micrometers became possible after blotting, i.e., after transferring lipids by physical contact with the substrate. The examples of pheromone-producing male hindwings of the squinting bush brown butterfly (Bicyclus anynana) and a fingermark are shown. Because the substrates are also easy to produce, they provide a viable alternative to colloidal silver nanoparticles and other so far described silver substrates. PMID:26827933

  15. Research progress in cation-π interactions

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Cation-π interaction is a potent intermolecular interaction between a cation and an aromatic system,which has been viewed as a new kind of binding force,as being compared with the classical interactions(e.g. hydrogen bonding,electrostatic and hydrophobic interactions). Cation-π interactions have been observed in a wide range of biological contexts. In this paper,we present an overview of the typical cation-π interactions in biological systems,the experimental and theoretical investigations on cation-π interactions,as well as the research results on cation-π interactions in our group.

  16. Research progress in cation-π interactions

    Institute of Scientific and Technical Information of China (English)

    CHENG JiaGao; LUO XiaoMin; YAN XiuHua; LI Zhong; TANG Yun; JIANG HuaLiang; ZHU WeiLiang

    2008-01-01

    Cation-π interaction is a potent intermolecular interaction between a cation and an aromatic system, which has been viewed as a new kind of binding force, as being compared with the classical interac-tions (e.g. hydrogen bonding, electrostatic and hydrophobic interactions). Cation-π interactions have been observed in a wide range of biological contexts. In this paper, we present an overview of the typi-cal cation-π interactions in biological systems, the experimental and theoretical investigations on cation-π interactions, as well as the research results on cation-π interactions in our group.

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

    Directory of Open Access Journals (Sweden)

    Sirikamon Saengmee-anupharb

    2013-01-01

    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.

  18. Oral toxicity of silver ions, silver nanoparticles and colloidal silver – a review

    DEFF Research Database (Denmark)

    Hadrup, Niels; Lam, Henrik Rye

    2014-01-01

    Orally administered silver has been described to be absorbed in a range of 0.4-18% in mammals with a human value of 18%. Based on findings in animals, silver seems to be distributed to all of the organs investigated, with the highest levels being observed in the intestine and stomach. In the skin...

  19. Silver-Palladium Surfaces Inhibit Biofilm Formation

    DEFF Research Database (Denmark)

    Chiang, Wen-Chi; Schroll, Casper; Hilbert, Lisbeth Rischel;

    2009-01-01

    efficacy and study of the biofilm inhibition mechanism, the silver-sensitive Escherichia coli J53 and the silver-resistant E. coli J53[pMG101] strains were used as model organisms, and batch and flow chamber setups were used as model systems. In the case of the silver-sensitive strain, the silver...

  20. A Silver DNAzyme.

    Science.gov (United States)

    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. Optics of Nanostructured Fractal Silver Colloids

    CERN Document Server

    Karpov, S V; Popov, A K; Slabko, V V; George, T F; George, Thomas F.

    2003-01-01

    Based on the theory of the optical properties of fractal clusters, which is an operator-based modification of the coupled-dipole method, an alternate solution is proposed for the problem of adequately describing the evolution of optical spectra of any polydisperse silver colloid with particles falling within the range of most characteristic sizes (5 - 30 nm). This is the range over which the results of the application of the well-known methods of classical electrodynamics, including the Mie theory, disagree with experimental data. The effect of variation of the parameters of such media on optical spectra is studied by a numerical simulation, which accounts for particle electrodynamic dipole-dipole interactions. Indeed, such interactions are shown to be a key factor in determining the broadening of the sol absorption spectra during the course of fractal aggregation. A quantitative explanation is given for the reasons for the appearance of individual specific features in the contours of the spectral absorption ...

  2. Tripodal Receptors for Cation and Anion Sensors

    NARCIS (Netherlands)

    Kuswandi, Bambang; Nuriman,; Verboom, Willem; Reinhoudt, David N.

    2006-01-01

    This review discusses different types of artificial tripodal receptors for the selectiverecognition and sensing of cations and anions. Examples on the relationship between structure andselectivity towards cations and anions are described. Furthermore, their applications as potentiometricion sensing

  3. Features definition exchange cations in sedimentary rocks.

    OpenAIRE

    Bilec'ka V.A.

    2008-01-01

    The research method of determination of exchange cations in calcareous sedimentary rocks of different extractants, the influence of the ratio between the solid and liquid phases on extrusion exchange cations.

  4. Features definition exchange cations in sedimentary rocks.

    Directory of Open Access Journals (Sweden)

    Bilec'ka V.A.

    2008-05-01

    Full Text Available The research method of determination of exchange cations in calcareous sedimentary rocks of different extractants, the influence of the ratio between the solid and liquid phases on extrusion exchange cations.

  5. MOD silver metallization for photovoltaics

    Science.gov (United States)

    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.

  6. Antibacterial effect of silver modified TiO2/PECVD films

    Science.gov (United States)

    Hájková, P.; Patenka, P. Å.; Krumeich, J.; Exnar, P.; Kolouch, A.; Matoušek, J.; Kočí, P.

    2009-08-01

    This paper deals with photocatalytic activity of silver treated TiO2 films. The TiO2 films were deposited on glass substrates by plasma enhanced chemical vapor deposition (PECVD) in a vacuum reactor with radio frequency (RF) low temperature plasma discharge in the mixture of oxygen and titanium isopropoxide vapors (TTIP). The depositions were performed under different deposition conditions. Subsequently, the surface of TiO2 films was modified by deposition of silver nanoparticles. Photocatalytic activity of both silver modified and unmodified TiO2 films was determined by decomposition of the model organic matter (acid orange 7). Selected TiO2 samples were used for tests of antibacterial activity. These tests were performed on Gram-negative bacteria Escherichia coli. The results clearly proved that presence of silver clusters resulted in enhancement of the photocatalytic activity, which was up to four times higher than that for pure TiO2 films.

  7. Isotopic clusters

    International Nuclear Information System (INIS)

    Spectra of isotopically mixed clusters (dimers of SF6) are calculated as well as transition frequencies. The result leads to speculations about the suitability of the laser-cluster fragmentation process for isotope separation. (Auth.)

  8. Cationic electrodepositable coating composition comprising lignin

    Science.gov (United States)

    Fenn, David; Bowman, Mark P; Zawacky, Steven R; Van Buskirk, Ellor J; Kamarchik, Peter

    2013-07-30

    A cationic electrodepositable coating composition is disclosed. The present invention in directed to a cationic electrodepositable coating composition comprising a lignin-containing cationic salt resin, that comprises (A) the reaction product of: lignin, an amine, and a carbonyl compound; (B) the reaction product of lignin, epichlorohydrin, and an amine; or (C) combinations thereof.

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

    Science.gov (United States)

    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

  10. Organometallic cation-exchanged phyllosilicates

    OpenAIRE

    Fleming, Shay

    1991-01-01

    Organotin (IV) complexes formed between 0 01 M dimethyltin dichloride solutions prepared at pH 2 6 and 4 0, and trimethyltin chloride prepared at pH 3 4, with Na- 119 montmori 1lonite clay have been characterised using Sn Mflssbauer spectroscopy, X-ray diffraction, thermogravimetric analysis and water sorption isotherms Following cation exchange, Mttssbauer spectroscopy identified two tin species in the dimethyltin (IV)-exchanged clay prepared at pH 2 6 A cis specie...

  11. Structural evolution in the crystallization of rapid cooling silver melt

    Energy Technology Data Exchange (ETDEWEB)

    Tian, Z.A., E-mail: ze.tian@gmail.com [School of Physics and Electronics, Hunan University, Changsha 410082 (China); Laboratory for Simulation and Modelling of Particulate Systems School of Materials Science and Engineering, University of New South Wales, Sydney, NSW 2052 (Australia); Dong, K.J.; Yu, A.B. [Laboratory for Simulation and Modelling of Particulate Systems School of Materials Science and Engineering, University of New South Wales, Sydney, NSW 2052 (Australia)

    2015-03-15

    The structural evolution in a rapid cooling process of silver melt has been investigated at different scales by adopting several analysis methods. The results testify Ostwald’s rule of stages and Frank conjecture upon icosahedron with many specific details. In particular, the cluster-scale analysis by a recent developed method called LSCA (the Largest Standard Cluster Analysis) clarified the complex structural evolution occurred in crystallization: different kinds of local clusters (such as ico-like (ico is the abbreviation of icosahedron), ico-bcc like (bcc, body-centred cubic), bcc, bcc-like structures) in turn have their maximal numbers as temperature decreases. And in a rather wide temperature range the icosahedral short-range order (ISRO) demonstrates a saturated stage (where the amount of ico-like structures keeps stable) that breeds metastable bcc clusters. As the precursor of crystallization, after reaching the maximal number bcc clusters finally decrease, resulting in the final solid being a mixture mainly composed of fcc/hcp (face-centred cubic and hexagonal-closed packed) clusters and to a less degree, bcc clusters. This detailed geometric picture for crystallization of liquid metal is believed to be useful to improve the fundamental understanding of liquid–solid phase transition. - Highlights: • A comprehensive structural analysis is conducted focusing on crystallization. • The involved atoms in our analysis are more than 90% for all samples concerned. • A series of distinct intermediate states are found in crystallization of silver melt. • A novelty icosahedron-saturated state breeds the metastable bcc state.

  12. Meaningful Clusters

    Energy Technology Data Exchange (ETDEWEB)

    Sanfilippo, Antonio P.; Calapristi, Augustin J.; Crow, Vernon L.; Hetzler, Elizabeth G.; Turner, Alan E.

    2004-05-26

    We present an approach to the disambiguation of cluster labels that capitalizes on the notion of semantic similarity to assign WordNet senses to cluster labels. The approach provides interesting insights on how document clustering can provide the basis for developing a novel approach to word sense disambiguation.

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

    Institute of Scientific and Technical Information of China (English)

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

    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, Candidaalbicans 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.

  14. Electrodeposition of silver nanodendrites

    Energy Technology Data Exchange (ETDEWEB)

    Kaniyankandy, Sreejith [Chemistry Division, Bhabha Atomic Research Centre, Mumbai (India); Nuwad, J [Chemistry Division, Bhabha Atomic Research Centre, Mumbai (India); Thinaharan, C [Technical Physics and Prototype Engineering Division, Bhabha Atomic Research Centre, Mumbai (India); Dey, G K [Materials Science Division, Bhabha Atomic Research Centre, Mumbai (India); Pillai, C G S [Chemistry Division, Bhabha Atomic Research Centre, Mumbai (India)

    2007-03-28

    Nanodendrites of silver were synthesized by electrodeposition using AgNO{sub 3} as the source in ammoniacal solution. The method was remarkably fast, simple and scalable. X-ray diffraction (XRD) studies confirmed the formation of a cubic phase of silver. Scanning electron microscopy (SEM) revealed the formation of well-shaped dendrites. The nanodendrites were hyperbranched with lengths of the order of a few micrometres. The concentration of NH{sub 3} in the electrolyte solution was found to have remarkable influence on the morphology, crystallite size and formation of branched nanodendrites. The branchings were found to occur at regular intervals of {approx}50 nm along the main stem. Transmission electron microscopy (TEM) studies confirmed the SEM observation and revealed the 2D nature of the dendrites. Selected area electron diffraction (SAED) revealed that the dendrites were single crystalline in nature and the branching could have a crystalline origin. The direction of growth as inferred from SAED was <110>. UV-vis spectra showed a single broad band centred on {approx}380 nm indicating the spherical shape of the individual crystallites. The intrinsic size effect of the metal surface plasmon was used to explain the increase in the broadening on addition of NH{sub 3}. The asymmetry of the band was explained on the basis of agglomeration of crystallites. The nanodendrites prepared by this method showed extension of the plasmon band through the entire visible region, indicating potential use in detection of single molecules based on enhanced Raman scattering. The deposition mechanism is described using the diffusion-limited aggregation model.

  15. Discovery of the Silver Isotopes

    OpenAIRE

    Schuh, A.; A. Fritsch; Ginepro, J. Q.; Heim, M.; SHORE, A.; Thoennessen, M

    2009-01-01

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

  16. Silver Nafion for Thermogalvanic Applications

    Science.gov (United States)

    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. Silver metallization stability and reliability

    CERN Document Server

    Adams, Daniel; Mayer, James W

    2007-01-01

    Anyone involved in circuit technology will find this an absolute must-read. It's the first book to discuss the current understanding of silver metallization and its potential as a future interconnect material for integrated circuit technology.

  18. Redox potential tuning by redox-inactive cations in nature's water oxidizing catalyst and synthetic analogues.

    Science.gov (United States)

    Krewald, Vera; Neese, Frank; Pantazis, Dimitrios A

    2016-04-28

    The redox potential of synthetic oligonuclear transition metal complexes has been shown to correlate with the Lewis acidity of a redox-inactive cation connected to the redox-active transition metals of the cluster via oxo or hydroxo bridges. Such heterometallic clusters are important cofactors in many metalloenzymes, where it is speculated that the redox-inactive constituent ion of the cluster serves to optimize its redox potential for electron transfer or catalysis. A principal example is the oxygen-evolving complex in photosystem II of natural photosynthesis, a Mn4CaO5 cofactor that oxidizes water into dioxygen, protons and electrons. Calcium is critical for catalytic function, but its precise role is not yet established. In analogy to synthetic complexes it has been suggested that Ca(2+) fine-tunes the redox potential of the manganese cluster. Here we evaluate this hypothesis by computing the relative redox potentials of substituted derivatives of the oxygen-evolving complex with the cations Sr(2+), Gd(3+), Cd(2+), Zn(2+), Mg(2+), Sc(3+), Na(+) and Y(3+) for two sequential transitions of its catalytic cycle. The theoretical approach is validated with a series of experimentally well-characterized Mn3AO4 cubane complexes that are structural mimics of the enzymatic cluster. Our results reproduce perfectly the experimentally observed correlation between the redox potential and the Lewis acidities of redox-inactive cations for the synthetic complexes. However, it is conclusively demonstrated that this correlation does not hold for the oxygen evolving complex. In the enzyme the redox potential of the cluster only responds to the charge of the redox-inactive cations and remains otherwise insensitive to their precise identity, precluding redox-tuning of the metal cluster as a primary role for Ca(2+) in biological water oxidation.

  19. Data Clustering

    Science.gov (United States)

    Wagstaff, Kiri L.

    2012-03-01

    On obtaining a new data set, the researcher is immediately faced with the challenge of obtaining a high-level understanding from the observations. What does a typical item look like? What are the dominant trends? How many distinct groups are included in the data set, and how is each one characterized? Which observable values are common, and which rarely occur? Which items stand out as anomalies or outliers from the rest of the data? This challenge is exacerbated by the steady growth in data set size [11] as new instruments push into new frontiers of parameter space, via improvements in temporal, spatial, and spectral resolution, or by the desire to "fuse" observations from different modalities and instruments into a larger-picture understanding of the same underlying phenomenon. Data clustering algorithms provide a variety of solutions for this task. They can generate summaries, locate outliers, compress data, identify dense or sparse regions of feature space, and build data models. It is useful to note up front that "clusters" in this context refer to groups of items within some descriptive feature space, not (necessarily) to "galaxy clusters" which are dense regions in physical space. The goal of this chapter is to survey a variety of data clustering methods, with an eye toward their applicability to astronomical data analysis. In addition to improving the individual researcher’s understanding of a given data set, clustering has led directly to scientific advances, such as the discovery of new subclasses of stars [14] and gamma-ray bursts (GRBs) [38]. All clustering algorithms seek to identify groups within a data set that reflect some observed, quantifiable structure. Clustering is traditionally an unsupervised approach to data analysis, in the sense that it operates without any direct guidance about which items should be assigned to which clusters. There has been a recent trend in the clustering literature toward supporting semisupervised or constrained

  20. Use of laser induced photoacoustic spectroscopy (LIPAS) to determine equilibrium constants of cation-cation complexes

    International Nuclear Information System (INIS)

    Laser Induced PhotoAcoustic Spectroscopy (LIPAS) is a relatively new, photothermal technique to examine solutions. Studies in the past have shown it to be more sensitive than conventional absorption spectroscopy, while, yielding the same information thus allowing lower concentrations to be used. This study is using LIPAS to examine solutions to determine the equilibrium constants of cation-cation complexes. It has been found that actinyl(V) cations form cation-cation complexes with a variety of cations, including actinyl(VI) cations. The radioactive nature of the actinide elements requires special handling techniques and also require limits be placed on the amount of material that can be used. The sensitivity of some oxidation states of the actinides to oxygen also presents a problem. Preliminary results will be presented for actinyl(V)-actinyl(VI) cation-cation complexes that were studied using a remote LIPAS system incorporating fiber optics for transmission of laser signals

  1. Detection of target DNA using fluorescent cationic polymer and peptide nucleic acid probes on solid support

    Directory of Open Access Journals (Sweden)

    Leclerc Mario

    2005-04-01

    Full Text Available Abstract Background Nucleic acids detection using microarrays requires labelling of target nucleic acids with fluorophores or other reporter molecules prior to hybridization. Results Using surface-bound peptide nucleic acids (PNA probes and soluble fluorescent cationic polythiophenes, we show a simple and sensitive electrostatic approach to detect and identify unlabelled target nucleic acid on microarray. Conclusion This simple methodology opens exciting possibilities for applied genetic analysis for the diagnosis of infections, identification of genetic mutations, and forensic inquiries. This electrostatic strategy could also be used with other nucleic acid detection methods such as electrochemistry, silver staining, metallization, quantum dots, or electrochemical dyes.

  2. Investigation on silver complexes of novel 1,2,3-triazole linked crown ethers by NMR analysis

    Indian Academy of Sciences (India)

    Piotr Seliger; Natalia Gutowska; Monika Stefaniak; Jarosław Romański

    2015-10-01

    The novel derivatives of 1,2,3-triazole linked crown ethers were investigated towards silver(I) ion coordination. The NMR measurements in deuterated methanol in different ratios of ligand and silver cation were studied. The experiments were performed in order to examine the way of binding Ag(I) ion by the selected ligands. The results are presented for complexes with the Ag:L stoichiometry 0.5:1, 1:1 and 2:1, respectively. Depending on the type of crown ether moiety incorporated into the macrocyclic skeleton, interesting differences in the mode of stepwise coordination of the ion were noticed.

  3. The Free Tricoordinated Silyl Cation Problem

    Directory of Open Access Journals (Sweden)

    Čičak, H.

    2010-03-01

    Full Text Available As the importance and abundance of silicon in our environment is large, it has been thought that silicon might take the place of carbon in forming a host of similar compounds and silicon-based life. However, until today there is no experimental evidence for such a hypothesis and carbon is still unique among the elements in the vast number and variety of compounds it can form. Also, the corresponding derivatives of the two elements show considerable differences in their chemical properties.The essential debate concerning organosilicon chemistry relates to the existence of the free planar tricoordinated silyl cations in condensed phase (R3Si+, in analogy to carbocations (R3C+ which have been known and characterized as free species. Although silyl cations are thermodynamically more stable than their carbon analogs, they are very reactive due to their high inherent electrophilicity and the ability of hypervalent coordination. On the other hand, stabilization by inductive and hyperconjugative effects and larger steric effects of carbocations make them less sensitive to solvation or other environmental effects than silyl cations. Hence, observation of free silyl cations in the condensed phase proved extremely difficult and the actual problem is the question of the degree of the (remaining silyl cation character.The first free silyl cation, trimesitylsilyl cation, and in analogy with it tridurylsilyl cation, were synthesized by Lambert et al. Free silyl cations based on analogy to aromatic ions (homocyclopropenylium and tropylium have also been prepared. However, in these silyl cations the cationic character is reduced by internal π -conjugation. Čičak et al. prepared some silyl-cationic intermediates (Me3Si--CH≡CR+in solid state. With the help of quantum-mechanical calculations it was concluded that these adducts have much more silyl cation than carbocation character.

  4. Distribution of silver in rats following 28 days of repeated oral exposure to silver nanoparticles or silver acetate

    OpenAIRE

    Mortensen Alicja; Vogel Ulla; Gao Xueyun; Larsen Agnete; Qvortrup Klaus; Hadrup Niels; Loeschner Katrin; Lam Henrik; Larsen Erik H

    2011-01-01

    Abstract Background The study investigated the distribution of silver after 28 days repeated oral administration of silver nanoparticles (AgNPs) and silver acetate (AgAc) to rats. Oral administration is a relevant route of exposure because of the use of silver nanoparticles in products related to food and food contact materials. Results AgNPs were synthesized with a size distribution of 14 ± 4 nm in diameter (90% of the nanoparticle volume) and stabilized in aqueous suspension by the polymer ...

  5. A tetrakis(amido)phosphonium cation containing 2-pyridyl (2Py) substituents,[P(NH2Py)4]+ and its reactivity studies with Ag(I) salts

    Indian Academy of Sciences (India)

    Arvind K Gupta; Anant Kumar Srivastava; Ramamoorthy Boomishankar

    2015-04-01

    Poly-imido analogues of various phosphorus oxo anions have gained recent attention in inorganic chemistry. Current methods to obtain these anions require strong organometallic deprotonating agents in reaction with phosphonium salt like [(NHPh)4P]Cl or phosphoramides such as [(RNH)3P=E] (E = NSiMe3, O, S or Se) in non-polar solvents. Recently, employing salts of soft and reactive transition metal ions, we have developed methods to obtain these anions in polar and protic solvents. Herein, we have described a facile anion exchange route that stabilizes the highly labile tetrakis(2-pyridylamino)phosphonium cation as its nitrate salt, [P(NH2Py)4]NO3. This molecule exhibits a double chain structure mediated by H-bonding interactions of the pyridylamino segments (N-H...N). The phosphonium salt upon reaction with excess silver triflate results in a pentanuclear Ag(I) complex, {Ag5[P(N2Py)2(NH2Py)2]}·(F3CSO3)3, stabilized by two imido-phosphinate [P(N2Py)2(NH2Py)2]− ligands. Formation of a similar penta-nuclear cluster has been observed before when AgClO4 was used as a base. Our previous results with the related phosphate precursor, [PO(NH2Py)3], in reaction with various Ag(I) salts have shown to yield complexes of the corresponding neutral, mono- and dianionic ligands. However, the stability of the Ag5-cluster within the mono-anionic casing of the [P(N2Py)2(NH2Py)2]− ligand have seemingly overwhelmed the subtle reactivity changes offered by various Ag(I) salts.

  6. Cluster Chemistry

    Institute of Scientific and Technical Information of China (English)

    2011-01-01

    @@ Cansisting of eight scientists from the State Key Laboratory of Physical Chemistry of Solid Surfaces and Xiamen University, this creative research group is devoted to the research of cluster chemistry and creation of nanomaterials.After three-year hard work, the group scored a series of encouraging progresses in synthesis of clusters with special structures, including novel fullerenes, fullerene-like metal cluster compounds as well as other related nanomaterials, and their properties study.

  7. Structure Determination of Noble Metal Clusters by Trapped Ion Electron Diffraction

    Science.gov (United States)

    Schooss, Detlef

    2006-03-01

    The structures of noble metal cluster ions have been studied by the recently developed technique of trapped ion electron diffraction (TIED)^1. In brief, cluster ions are generated by a magnetron sputter source and injected into a cooled (95 K) quadrupole ion trap. After mass selection and thermalization, the trapped ions are irradiated with a 40 keV electron beam. The resulting diffraction pattern is integrated with a CCD detector. The assignment of the structural motif is done via a comparison of the experimental and simulated scattering function, calculated from density functional theory structure calculations. The structures of mass selected silver cluster cations Ag19^+, Ag38^+, Ag55^+, Ag59^+, Ag75^+ and Ag79^+ have been investigated^2. The resulting experimental data are best described by structures based on the icosahedral motif, while closed packed structures could be ruled out. Additionally, we present a comparison of the structures of Cu20^+/-, Ag20^+/- and Au20^+/-. Our findings show unambiguously that the structure of Au20^- is predominantly given by a tetrahedron in agreement with the results of L.S. Wang et al.^3 In contrast, structures of Ag20^- and Cu20^- based on the icosahedral motif agree best with the experimental data. Small structural differences between the charge states are observed. The possibilities and limitations of the TIED method are discussed. (1) M. Maier-Borst, D. B. Cameron, M. Rokni, and J. H. Parks, Physical Review A 59 (5), R3162 (1999); S. Krückeberg, D. Schooss, M. Maier-Borst, and J. H. Parks, Physical Review Letters 85 (21), 4494 (2000). (2) D. Schooss, M.N. Blom, B. v. Issendorff, J. H. Parks, and M.M. Kappes, Nano Letters 5 (10), 1972 (2005). (3) J. Li, X. Li, H. J. Zhai, and L. S. Wang, Science 299, 864 (2003)

  8. SERS Substrates by the Assembly of Silver Nano cubes: High-Throughput and Enhancement Reliability Considerations

    International Nuclear Information System (INIS)

    Small clusters of nanoparticles are ideal substrates for SERS measurements, but the SERS signal enhancement by a particular cluster is strongly dependent on its structural characteristics and the measurement conditions. Two methods for high-throughput assembly of silver nano cubes into small clusters at predetermined locations on a substrate are presented. These fabrication techniques make it possible to study both the structure and the plasmonic properties of hundreds of nanoparticle clusters. The variations in SERS enhancement factors from cluster to cluster were analyzed and correlated with cluster size and configuration, and laser frequency and polarization. Using Raman instruments with 633 nm and 785 nm lasers and linear clusters of nano cubes, an increase in the reproducibility of the enhancement and an increase in the average enhancement values were achieved by increasing the number of nano cubes in the cluster, up to 4 nano cubes per cluster. By examining the effect of cluster configuration, it is shown that linear clusters with nano cubes attached in a face-to-face configuration are not as effective SERS substrates as linear clusters in which nano cubes are attached along an edge

  9. The properties of small Ag clusters bound to DNA bases

    Science.gov (United States)

    Soto-Verdugo, Víctor; Metiu, Horia; Gwinn, Elisabeth

    2010-05-01

    We study the binding of neutral silver clusters, Agn (n=1-6), to the DNA bases adenine (A), cytosine (C), guanine (G), and thymine (T) and the absorption spectra of the silver cluster-base complexes. Using density functional theory (DFT), we find that the clusters prefer to bind to the doubly bonded ring nitrogens and that binding to T is generally much weaker than to C, G, and A. Ag3 and Ag4 make the stronger bonds. Bader charge analysis indicates a mild electron transfer from the base to the clusters for all bases, except T. The donor bases (C, G, and A) bind to the sites on the cluster where the lowest unoccupied molecular orbital has a pronounced protrusion. The site where cluster binds to the base is controlled by the shape of the higher occupied states of the base. Time-dependent DFT calculations show that different base-cluster isomers may have very different absorption spectra. In particular, we find new excitations in base-cluster molecules, at energies well below those of the isolated components, and with strengths that depend strongly on the orientations of planar clusters with respect to the base planes. Our results suggest that geometric constraints on binding, imposed by designed DNA structures, may be a feasible route to engineering the selection of specific cluster-base assemblies.

  10. Surface enhanced Raman scattering of melamine on silver substrate: An experimental and DFT study.

    Science.gov (United States)

    An, Nguyen Thi Thai; Dao, Duy Quang; Nam, Pham Cam; Huy, Bui The; Nhung Tran, Hong

    2016-12-01

    Surface enhanced Raman spectroscopy (SERS) is a powerful vibrational spectroscopy technique that allows amplifying weak Raman signals by the excitation of localized surface plasmons. In this paper, we used nanoscale roughened silver surface to enhance Raman signals of melamine analyte. Silver nanoparticles were synthesized by wet-chemical method and employed for SERS measurement. Theoretically, optimized geometries and vibrational frequencies of melamine and melamine absorbed on silver-cluster surface were calculated by using the B3LYP/6-31G(d) method. Then, the predicted spectrograms are compared with the experimental Raman spectra. As a result, Raman signals of melamine were dramatically enhanced by using obtained silver nanoparticles as the substrate. Typical peaks of melamine at 676 and 983cm(-1) were enhanced and could be obviously observed in experiments. The calculated vibrational frequencies seem to relatively coincide with the experimental values. SERS effect of melamine on nanoscale silver was also explained by analyzing molecular frontier orbitals (HOMO and LUMO) melamine-silver complexes.

  11. Silver Modified Degussa P25 for the Photocatalytic Removal of Nitric Oxide

    Directory of Open Access Journals (Sweden)

    Neil Bowering

    2007-01-01

    Full Text Available A study of the photocatalytic behaviour of silver modified titanium dioxide materials for the decomposition and reduction of nitric oxide (NO gas has been carried out. The effects of silver loading, calcination temperature, and reaction conditions have been investigated. Prepared photocatalysts were characterised using XRD, TEM, and XPS. A continuous flow reactor was used to determine the photocatalytic activity and selectivity of NO decomposition in the absence of oxygen as well as NO reduction using CO as the reducing agent, over the prepared photocatalysts. XRD and TEM analysis of the photocatalysts showed that crystalline silver nitrate particles were present on the titanium dioxide surface after calcination at temperatures of up to 200∘C. The silver nitrate particles are thermally decomposed to form metallic silver clusters at higher temperatures. XPS analysis of the photocatalysts showed that for each of the temperatures used, both Ag+ and Ag0 were present and that the Ag0/Ag+ ratio increased with increasing calcination temperature. The presence of metallic silver species on the TiO2 surface dramatically increased the selectivity for N2 formation of both decomposition and reduction reactions. When CO was present in the reaction gas, selectivities of over 90% were observed for all the Ag-TiO2 photocatalysts that had been calcined at temperatures above 200∘C. Unfortunately these high selectivities were at the expense of photocatalytic activity, with lower NO conversion rates than those achieved over unmodified TiO2 photocatalysts.

  12. Fuzzy Clustering

    DEFF Research Database (Denmark)

    Berks, G.; Keyserlingk, Diedrich Graf von; Jantzen, Jan;

    2000-01-01

    -mean clustering is an easy and well improved tool, which has been applied in many medical fields. We used c-mean fuzzy clustering after feature extraction from an aphasia database. Factor analysis was applied on a correlation matrix of 26 symptoms of language disorders and led to five factors. The factors...

  13. Single Molecule Raman Detection of Enkephalin on Silver Colloidal Particles

    DEFF Research Database (Denmark)

    Kneipp, Katrin; Kneipp, Holger; Abdali, Salim;

    2004-01-01

    Enkephalin, an endogeneous substance in the human brain showing morphine-like biological functions, has been detected at the single molecule level based on the surface-enhanced Raman signal of the ring breathing mode of phenylalanine, which is one building block of the molecule. For enhancing...... the Raman signal the enkephalin molecules have been attached to silver colloidal cluster structures. The experiments demonstrate that the SERS signal of the strongly enhanced ring breathing vibration of phenylalanine at 1000 cm-1 can be used as “intrinsic marker” for detecting a single enkephalin molecule...

  14. Afrikaans Syllabification Patterns

    Directory of Open Access Journals (Sweden)

    Tilla Fick

    2010-01-01

    Full Text Available In contrast to English, automatic hyphenation by computer of Afrikaans words is a problem that still needs to be addressed, since errors are still often encountered in printed text. An initial step in this task is the ability to automatically syllabify words. Since new words are created continuously by joining words, it is necessary to develop an “intelligent” technique for syllabification. As a first phase of the research, we consider only the orthographic information of words, and disregard both syntactic and morphological information. This approach allows us to use machine-learning techniques such as artificial neural networks and decision trees that are known for their pattern recognition abilities. Both these techniques are trained with isolated patterns consisting of input patterns and corresponding outputs (or targets that indicate whether the input pattern should be split at a certain position, or not. In the process of compiling a list of syllabified words from which to generate training data for the  syllabification problem, irregular patterns were identified. The same letter patterns are split differently in different words and complete words that are spelled identically are split differently due to meaning. We also identified irregularities in and between  the different dictionaries that we used. We examined the influence range of letters that are involved in irregularities. For example, for their in agter-ente and vaste-rente we have to consider three letters to the left of r to be certain where the hyphen should be inserted. The influence range of the k in verstek-waarde and kleinste-kwadrate is four to the left and three to the right. In an analysis of letter patterns in Afrikaans words we found that the letter e has the highest frequency overall (16,2% of all letters in the word list. The frequency of words starting with s is the highest, while the frequency of words ending with e is the highest. It is important to

  15. Antituberculous effect of silver nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Kreytsberg, G N; Gracheva, I E [Limited Liability Company ' Scientific and Production Association (NPO)' Likom' , 150049, Yaroslavl, Magistralnaya str., 32 (Russian Federation); Kibrik, B S [Yaroslavl State Medical Academy Russia, 150000, Yaroslavl, Revolutsionnaya str., 5 (Russian Federation); Golikov, I V, E-mail: likomm@yaroslavl.ru [Yaroslavl State Technical University Russia, 150023, Yaroslavl, Moskovskiy avenue, 88 (Russian Federation)

    2011-04-01

    The in vitro experiment, involving 1164 strains of the tuberculosis mycobacteria, exhibited a potentiating effect of silver nanoparticles on known antituberculous preparations in respect of overcoming drug-resistance of the causative agent. The in vitro experiment, based on the model of resistant tuberculosis, was performed on 65 white mice. An evident antituberculous effect of the nanocomposite on the basis of silver nanoparticles and isoniazid was proved. Toxicological assessment of the of nanopreparations was carried out. The performed research scientifically establishes efficacy and safety of the nanocomposite application in combination therapy of patients suffering from drug-resistant tuberculosis.

  16. Mineral resource of the month: silver

    Science.gov (United States)

    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.

  17. Chemistry of silver(II): a cornucopia of peculiarities†.

    Science.gov (United States)

    Grochala, Wojciech; Mazej, Zoran

    2015-03-13

    Silver is the heavier congener of copper in the Periodic Table, but the chemistry of these two elements is very different. While Cu(II) is the most common cationic form of copper, Ag(II) is rare and its compounds exhibit a broad range of peculiar physico-chemical properties. These include, but are not limited to: (i) uncommon oxidizing properties, (ii) unprecedented large mixing of metal and ligand valence orbitals, (iii) strong spin-polarization of neighbouring ligands, (iv) record large magnetic superexchange constants, (v) ease of thermal decomposition of its salts with O-, N- or C-ligands, as well as (vi) robust Jahn-Teller effect which is preserved even at high pressure. These intriguing features of the compounds of Ag(II) will be discussed here together with (vii) a possibility of electromerism (electronic tautomerism) for a certain class of Ag(II) salts. PMID:25666068

  18. Laser-induced reconstruction of Ag clusters in helium droplets

    Science.gov (United States)

    Gomez, Luis F.; O'Connell, Sean M. O.; Jones, Curtis F.; Kwok, Justin; Vilesov, Andrey F.

    2016-09-01

    Silver clusters were assembled in helium droplets of different sizes ranging from 105 to 1010 atoms. The absorption of the clusters was studied upon laser irradiation at 355 nm and 532 nm, which is close to the plasmon resonance maximum in spherical Ag clusters and in the range of the absorption of the complex, branched Ag clusters, respectively. The absorption of the pulsed (7 ns) radiation at 532 nm shows some pronounced saturation effects, absent upon the continuous irradiation. This phenomenon has been discussed in terms of the melting of the complex Ag clusters at high laser fluence, resulting in a loss of the 532 nm absorption. Estimates of the heat transfer also indicate that a bubble may be formed around the hot cluster at high fluences, which may result in ejection of the cluster from the droplet, or disintegration of the droplet entirely.

  19. Detection of silver(I) ion based on mixed surfactant-adsorbed CdS quantum dots

    International Nuclear Information System (INIS)

    Mixed cationic and anionic surfactants were adsorbed on cadmium sulfide quantum dots (CdS QDs) capped with mercaptoacetic acid. The CdS QDs can be extracted into acetonitrile with 98 % efficiency in a single step. Phase separation only occurs at a molar ratio of 1:1.5 between cationic and anionic surfactants. The surfactant-adsorbed QDs in acetonitrile solution display stronger and more stable photoluminescence than in water solution. The method was applied for determination of silver(I) ion based on its luminescence enhancement of the QDs. Under the optimum conditions, the relative fluorescence intensity is linearly proportional to the concentration of silver(I) ion in the range between 50 pmol L−1and 4 μmol L−1, with a 20 pmol L−1 detection limit. The relative standard deviation was 1.93 % for 9 replicate measurements of a 0.2 μmol L−1 solution of Ag(I). (author)

  20. Weighted Clustering

    CERN Document Server

    Ackerman, Margareta; Branzei, Simina; Loker, David

    2011-01-01

    In this paper we investigate clustering in the weighted setting, in which every data point is assigned a real valued weight. We conduct a theoretical analysis on the influence of weighted data on standard clustering algorithms in each of the partitional and hierarchical settings, characterising the precise conditions under which such algorithms react to weights, and classifying clustering methods into three broad categories: weight-responsive, weight-considering, and weight-robust. Our analysis raises several interesting questions and can be directly mapped to the classical unweighted setting.

  1. Cluster analysis

    CERN Document Server

    Everitt, Brian S; Leese, Morven; Stahl, Daniel

    2011-01-01

    Cluster analysis comprises a range of methods for classifying multivariate data into subgroups. By organizing multivariate data into such subgroups, clustering can help reveal the characteristics of any structure or patterns present. These techniques have proven useful in a wide range of areas such as medicine, psychology, market research and bioinformatics.This fifth edition of the highly successful Cluster Analysis includes coverage of the latest developments in the field and a new chapter dealing with finite mixture models for structured data.Real life examples are used throughout to demons

  2. Cluster editing

    DEFF Research Database (Denmark)

    Böcker, S.; Baumbach, Jan

    2013-01-01

    The Cluster Editing problem asks to transform a graph into a disjoint union of cliques using a minimum number of edge modifications. Although the problem has been proven NP-complete several times, it has nevertheless attracted much research both from the theoretical and the applied side. The...... algorithms for biological problems. © 2013 Springer-Verlag....... problem has been the inspiration for numerous algorithms in bioinformatics, aiming at clustering entities such as genes, proteins, phenotypes, or patients. In this paper, we review exact and heuristic methods that have been proposed for the Cluster Editing problem, and also applications of these...

  3. Silver metal colloidal film on a flexible polymer substrate

    Science.gov (United States)

    del Rocío Balaguera Gelves, Marcia; El Burai-Félix, Alia; De La Cruz-Montoya, Edwin; Jeréz Rozo, Jaqueline I.; Hernández-Rivera, Samuel P.

    2006-05-01

    A method to prepare metallic nanoparticles films in the presence of a hydrophilic copolymer with the aim of inhibiting the formation of clusters in the nanoparticles has been developed. Thin films prepared could be used in applications such as sensors development and substrates for surface-enhanced Raman spectroscopy. The synthesis of colloidal solutions of silver nanoparticles was achieved by the reduction AgNO 3 using sodium citrate with thermal treatment which results in a robust fabrication of gold and silver films. The polymeric films were prepared by polymerization 2-hydroxyethyl methacrylate with methacrylic acid (method 1). The other procedure employed (method 2) incorporated the use of polyvinyl pyrrolidone and polyethylene glycol as copolymers. A scanning electron microscope was used to provide microstructural information of coverage achieved. The ability to tune the nanocoating structure and spectral and electronic properties can be used for applications such as sensors used in the detection of explosives. Silver nanoparticles were also characterized by surface-enhanced Raman scattering (SERS), which integrates high chemical sensitivity with spectroscopic identification and has enormous potential for applications involving ultra-sensitive chemical detection. Spectra were obtained using a Renishaw RM2000 Raman Microspectrometer system operating in the visible region excitation (532 nm).

  4. SILVER NANOPARTICLES SYNTHESIZED BY THE AZERBAIJANIAN ENVIRONMENTAL ISOLATES ASPERGILLUS NIGER

    Directory of Open Access Journals (Sweden)

    Kh. G. Ganbarov

    2014-10-01

    Full Text Available The synthesis of nanoparticles by microorganisms is environmentally safe method. The silver nanoparticles produced by fungi is complex material having different size, shape and other properties depending on the producer. İt is necessary to study new microbial strains to synthesize silver nanoparticles with important properties. The synthesis of different stable silver nanoparticles by the mold fungi was investigated in this work. To achieve this goal different strains (isolates of Aspergillus niger were used. The most intensive formation of nanoparticles was observed in strains Aspergillus niger BDU-A4, BDU-K8, BDU-UB1 and BDU-UB5.While examining nanoparticles the following analysis methods were used: UV-Visible Spectroscopy, Scanning Electron Microscopy (SEM and Energy Dispersive Spectroscopy. Electron microscopic examination showed that the shape, size and nature of nanoparticles’ clusters were dependent on fungal strains. The shape of nanoparticles is usually circular but it may be oval like in case of nanoclusters consisting of a few spherical nanoparticles. Their size varies from 20 to 100 nm.The formation of free ellipsoidal shape nanoparticles was observed at strain of Aspergillus niger BDU-K8, that varies in the range 62,9 - 68,4 nm.

  5. Draft genome sequence of the silver pomfret fish, Pampus argenteus.

    Science.gov (United States)

    AlMomin, Sabah; Kumar, Vinod; Al-Amad, Sami; Al-Hussaini, Mohsen; Dashti, Talal; Al-Enezi, Khaznah; Akbar, Abrar

    2016-01-01

    Silver pomfret, Pampus argenteus, is a fish species from coastal waters. Despite its high commercial value, this edible fish has not been sequenced. Hence, its genetic and genomic studies have been limited. We report the first draft genome sequence of the silver pomfret obtained using a Next Generation Sequencing (NGS) technology. We assembled 38.7 Gb of nucleotides into scaffolds of 350 Mb with N50 of about 1.5 kb, using high quality paired end reads. These scaffolds represent 63.7% of the estimated silver pomfret genome length. The newly sequenced and assembled genome has 11.06% repetitive DNA regions, and this percentage is comparable to that of the tilapia genome. The genome analysis predicted 16 322 genes. About 91% of these genes showed homology with known proteins. Many gene clusters were annotated to protein and fatty-acid metabolism pathways that may be important in the context of the meat texture and immune system developmental processes. The reference genome can pave the way for the identification of many other genomic features that could improve breeding and population-management strategies, and it can also help characterize the genetic diversity of P. argenteus.

  6. Gravimetric and volumetric determination of the purity of electrolytically refined silver and the produced silver nitrate

    Directory of Open Access Journals (Sweden)

    Ačanski Marijana M.

    2007-01-01

    Full Text Available Silver is, along with gold and the platinum-group metals, one of the so called precious metals. Because of its comparative scarcity, brilliant white color, malleability and resistance to atmospheric oxidation, silver has been used in the manufacture of coins and jewelry for a long time. Silver has the highest known electrical and thermal conductivity of all metals and is used in fabricating printed electrical circuits, and also as a coating for electronic conductors. It is also alloyed with other elements such as nickel or palladium for use in electrical contacts. The most useful silver salt is silver nitrate, a caustic chemical reagent, significant as an antiseptic and as a reagent in analytical chemistry. Pure silver nitrate is an intermediate in the industrial preparation of other silver salts, including the colloidal silver compounds used in medicine and the silver halides incorporated into photographic emulsions. Silver halides become increasingly insoluble in the series: AgCl, AgBr, AgI. All silver salts are sensitive to light and are used in photographic coatings on film and paper. The ZORKA-PHARMA company (Sabac, Serbia specializes in the production of pharmaceutical remedies and lab chemicals. One of its products is chemical silver nitrate (argentum-nitricum (l. Silver nitrate is generally produced by dissolving pure electrolytically refined silver in hot 48% nitric acid. Since the purity of silver nitrate, produced in 2002, was not in compliance with the p.a. level of purity, there was doubt that the electrolytically refined silver was pure. The aim of this research was the gravimetric and volumetric determination of the purity of electrolytically refined silver and silver nitrate, produced industrially and in a laboratory. The purity determination was carried out gravimetrically, by the sedimentation of silver(I ions in the form of insoluble silver salts: AgCl, AgBr and Agi, and volumetrically, according to Mohr and Volhardt. The

  7. Localization versus delocalization in diamine radical cations

    DEFF Research Database (Denmark)

    Brouwer, A.M.; Wiering, P.G.; Zwier, J.M.;

    1997-01-01

    The optical absorption spectrum of the radical cation of 1,4-diphenylpiperazine 2a shows a strong transition in the near-IR, and only a weak band at 445 nm, in the region where aniline radical cations normally absorb strongly. This indicates that the charge and spin are delocalized over the two...

  8. Tripodal Receptors for Cation and Anion Sensors

    Directory of Open Access Journals (Sweden)

    David N. Reinhoudt

    2006-08-01

    Full Text Available This review discusses different types of artificial tripodal receptors for the selectiverecognition and sensing of cations and anions. Examples on the relationship between structure andselectivity towards cations and anions are described. Furthermore, their applications as potentiometricion sensing are emphasised, along with their potential applications in optical sensors or optodes.

  9. Influence of injected silver content on synthesis of silver coated nickel particles by DC thermal plasma

    Science.gov (United States)

    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.

  10. Evaluation of the influence of sulfur-based functional groups on the embedding of silver nanoparticles into the pores of MCM-41

    Science.gov (United States)

    Oliveira, Roselaine da S.; Camilo, Fernanda F.; Bizeto, Marcos A.

    2016-03-01

    The incorporation of noble metals in the pores of mesoporous silicas might produce materials with interesting catalytic and sensing capabilities, but the proper control of pore filling and the avoidance of nanoparticles migration to outside the pores are processes not yet completely understood. In this work, we evaluated the role of -SH and -SO3H groups post-grafted into MCM-41 on the production of silver nanoparticles by using 1-butanol as reducing agent. Thiol groups were the most efficient on promoting the formation of nanoparticles within the pores. Conversely, sulfonic groups establish electrostatic interactions with silver cations that preclude the formation of nanoparticle in yields comparable to thiol groups. MCM-41 without functional groups did not have good affinity to silver and the nanoparticles are produced outside the pores. This study showed the importance on selecting an adequate surface functional group in order to obtain silver nanoparticles filling the pores of MCM-41.

  11. A new alternative for the decontamination of PWR primary circuits for radioactive cesium and silver by insoluble ferrocyanides

    International Nuclear Information System (INIS)

    The optimal recovery conditions of radioactive cesium and silver from PWR primary circuits were determined on two types of nickel and zinc ferrocyanides. The studied products have been prepared by a slow growth on solid alkaline ferrocyanide particles placed in a concentrated nickel or zinc salt solution. Columns of these products do not react with water or lithium borate solutions as well as with organic solvents. The decontamination factor for cesium or silver is over 1000 for synthetic solutions. The presence of other alkaline ions does not modify these results. In the case of nuclear liquid wastes, the decontamination remains high for cesium. Silver is retained with a good efficiency if it is not under a complex form. This complex is destroyed by acidification. The setting of concrete is not significantly modified by the presence of ferrocyanides. The drawback of this method is a slight elution of some cations composing the ferrocyanides

  12. Solid phase extraction of ultra traces silver(I) using octadecyl silica membrane disks modified by 1,3-bis(2-cyanobenzene) triazene (CBT) ligand prior to determination by flame atomic absorption

    Energy Technology Data Exchange (ETDEWEB)

    Rofouei, Mohammad Kazem, E-mail: rofouei@tmu.ac.ir [Faculty of Chemistry, Tarbiat Moalem University, Tehran (Iran, Islamic Republic of); Payehghadr, Mahmood [Department of Chemistry, Payame Noor University (PNU) (Iran, Islamic Republic of); Shamsipur, Mojtaba [Department of Chemistry, Razi University, Kermanshah (Iran, Islamic Republic of); Ahmadalinezhad, Asieh [Department of Chemistry, Lakehead University, Thunder Bay, Ontario P7B 5E1 (Canada)

    2009-09-15

    A simple, reliable and rapid method for preconcentration and determination of the ultra trace amount of silver using octadecyl silica membrane disk modified by a recently synthesized triazene ligand, 1,3-bis(2-cyanobenzene)triazene (CBT), and flame atomic absorption spectrometry is presented. Various parameters including pH of aqueous solution, flow rates, the amount of ligand and the type of stripping solvents were optimized. The breakthrough volume was greater than 1800 ml with an enrichment factor of more than 360 and 6.0 ng l{sup -1} detection limit. The capacity of the membrane disks modified by 5 mg of the ligand was found to be 1070 {mu}g of silver. The effects of various cationic interferences on the percent recovery of silver ion were studied. The method was successfully applied to the determination of silver ion in different samples, especially determination of ultra trace amount of silver in the presence of large amount of lead.

  13. Plasmonic characterization of photo-induced silver nanoparticles extracted from silver halide based TEM film

    Science.gov (United States)

    Sudheer, Tiwari, P.; Varshney, G. K.; Rai, V. N.; Srivastava, A. K.

    2016-05-01

    The plasmonic responses of silver nanoparticles extracted from silver halide based electron microscope film are investigated. Photo-reduction process is carried out to convert the silver halide grains into the metallic silver. The centrifuge technique is used for separating the silver nanoparticles from the residual solution. Morphological study performed by field emission scanning electron microscope (FESEM) shows that all the nanoparticles have an average diameter of ~120 nm with a high degree of mono dispersion in size. The localized surface plasmon resonance (LSPR) absorption peak at ~537 nm confirms the presence of large size silver nanoparticles.

  14. PVDF membranes containing hybrid nanoparticles for adsorbing cationic dyes: physical insights and mechanism

    Science.gov (United States)

    Sharma, Maya; Madras, Giridhar; Bose, Suryasarathi

    2016-07-01

    In this study, Fe (iron) and Ag (silver) based adsorbents were synthesized using solution combustion and in situ reduction techniques. The synthesized adsorbents were comprehensively characterized by different techniques including electron microscopy, BET, XRD, Zeta potential etc. Three chlorinated cationic dyes used were malachite green, methyl violet and pyronin Y. These dyes were adsorbed on various synthesized adsorbents [iron III oxide (Fe2O3)], iron III oxide decorated silver nanoparticles by combustion synthesis technique [Fe2O3–Ag(C)] and iron III oxide decorated silver nanoparticles using in situ reduction, [Fe2O3–Ag (S)]. The isotherm and the adsorption kinetics have been studied systematically. The kinetic data can be explained by the pseudo second order model and the adsorption equilibrium followed Langmuir isotherm. The equilibrium and kinetics results suggest that Fe2O3–Ag(S) nanoparticles showed the maximum adsorption among all the adsorbents. Hence, Polyvinylidene fluoride based membranes containing Fe2O3–Ag(S) nanoparticles were prepared via phase inversion (precipitation immersion using DMF/water) technique. The adsorption kinetics were studied in detail and it was observed that the composite membrane showed synergistic improvement in dye adsorption. Such membranes can be used for water purification.

  15. Cationic Bolaamphiphiles for Gene Delivery

    Science.gov (United States)

    Tan, Amelia Li Min; Lim, Alisa Xue Ling; Zhu, Yiting; Yang, Yi Yan; Khan, Majad

    2014-05-01

    Advances in medical research have shed light on the genetic cause of many human diseases. Gene therapy is a promising approach which can be used to deliver therapeutic genes to treat genetic diseases at its most fundamental level. In general, nonviral vectors are preferred due to reduced risk of immune response, but they are also commonly associated with low transfection efficiency and high cytotoxicity. In contrast to viral vectors, nonviral vectors do not have a natural mechanism to overcome extra- and intracellular barriers when delivering the therapeutic gene into cell. Hence, its design has been increasingly complex to meet challenges faced in targeting of, penetration of and expression in a specific host cell in achieving more satisfactory transfection efficiency. Flexibility in design of the vector is desirable, to enable a careful and controlled manipulation of its properties and functions. This can be met by the use of bolaamphiphile, a special class of lipid. Unlike conventional lipids, bolaamphiphiles can form asymmetric complexes with the therapeutic gene. The advantage of having an asymmetric complex lies in the different purposes served by the interior and exterior of the complex. More effective gene encapsulation within the interior of the complex can be achieved without triggering greater aggregation of serum proteins with the exterior, potentially overcoming one of the great hurdles faced by conventional single-head cationic lipids. In this review, we will look into the physiochemical considerations as well as the biological aspects of a bolaamphiphile-based gene delivery system.

  16. Growth process of nanostructured silver films pulsed laser ablated in high-pressure inert gas

    International Nuclear Information System (INIS)

    The growth process of silver thin films deposited by pulsed laser ablation in a controlled inert gas atmosphere was investigated. A pure silver target was ablated in Ar atmosphere, at pressures ranging between 10 and 100 Pa, higher than usually adopted for thin film deposition, at different numbers of laser shots. All of the other experimental conditions such as the laser (KrF, wavelength 248 nm), the fluence of 2.0 J cm-2, the target to substrate distance of 35 mm, and the temperature (295 K) of the substrates were kept fixed. The morphological properties of the films were investigated by transmission and scanning electron microscopies (TEM, SEM). Film formation results from coalescence on the substrate of near-spherical silver clusters landing as isolated particles with size in the few nanometers range. From a visual inspection of TEM pictures of the films deposited under different conditions, well-separated stages of film growth are identified.

  17. Facile Preparation of Silver Nanoparticles and Application to Silver Coating Using Latent Reductant from a Silver Carbamate Complex

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Kyunga; Cha, Jaeryung; Gong, Myoungseon [Dankook Univ. Graduate School, Chungnam (Korea, Republic of)

    2013-02-15

    A low temperature (65 .deg. C) thermal deposition process was developed for depositing a silver coating on thermally sensitive polymeric substrates. This low temperature deposition was achieved by chemical reduction of a silver alkylcarbamate complex with latent reducing agent. The effects of acetol as a latent reducing agent for the silver 2-ethylhexylcarbamate (Ag-EHCB) complex and their blend solutions were investigated in terms of reducing mechanism, and the size and shape of silver nanoparticles (Ag-NPs) as a function of reduced temperature and time, and PVP stabilizer concentration were determined. Low temperature deposition was achieved by combining chemical reduction with thermal heating at 65 .deg. C. A range of polymer film, sheet and molding product was coated with silver at thicknesses of 100 nm. The effect of process parameters and heat treatment on the properties of silver coatings was investigated.

  18. Distribution of silver in rats following 28 days of repeated oral exposure to silver nanoparticles or silver acetate

    DEFF Research Database (Denmark)

    Löschner, Katrin; Hadrup, Niels; Qvortrup, Klaus;

    2011-01-01

    in rats. The organ distribution pattern of silver following administration of AgNPs and AgAc was similar. However the absolute silver concentrations in tissues were lower following oral exposure to AgNPs. This was in agreement with an indication of a higher fecal excretion following administration of Ag......Background: The study investigated the distribution of silver after 28 days repeated oral administration of silver nanoparticles (AgNPs) and silver acetate (AgAc) to rats. Oral administration is a relevant route of exposure because of the use of silver nanoparticles in products related to food...... and food contact materials. Results: AgNPs were synthesized with a size distribution of 14 ± 4 nm in diameter (90% of the nanoparticle volume) and stabilized in aqueous suspension by the polymer polyvinylpyrrolidone (PVP). The AgNPs remained stable throughout the duration of the 28-day oral toxicity study...

  19. Mechanistic study of silver-mediated furan formation by oxidative coupling.

    Science.gov (United States)

    Daru, János; Benda, Zsuzsanna; Póti, Ádám; Novák, Zoltán; Stirling, András

    2014-11-17

    Density functional calculations and experiments have been carried out to unravel the mechanism of a silver-mediated furan formation by oxidative coupling. Various possible reaction paths were considered and the most favorable channel has been identified on the basis of the calculated solvent-corrected Gibbs free-energy profiles. The mechanism represented by this route consists of a radical and a subsequent ionic route. The silver cation has a double role in the mechanism: it is the oxidant in the radical steps and the catalyst for the ionic steps, which is in accordance with the experimental observations. The two most important aspects of the optimal route are the formation of a silver-acetylide, reacting subsequently with the enolate radical, and the aromatic furan-ring formation in a single step at the latter, ionic segment of the reaction path. Our findings could explain several experimental observations, including the "key-promoter role" of silver, the preference for ionic cyclization, and the reduced reactivity of internal acetylides. PMID:25284602

  20. Environmentally Friendly Preparation of Gold and Silver Nanoparticles for Sers Applications Using Biopolymer Pectin

    Science.gov (United States)

    Balachandran, Y. L.; Panarin, A. Y.; Khodasevich, I. A.; Terekhov, S. N.; Gutleb, A. C.; Girijaa, S.

    2015-01-01

    A facile, one-step, and environmentally friendly fabrication of anisotropic gold nanostructures and size-controlled spherical silver nanoparticles (NP) using biopolymer pectin is reported. The reduction of Au and Ag ions was carried out at room temperature using an increasing concentration of pectin, which acts as the single source of reducing and stabilizing agent. The as-formed NPs were studied by UV-vis, infrared Fourier transform and surface-enhanced Raman spectroscopies, as well as transmission electron microscopy and energy dispersive X-ray spectroscopy. A high yield of anisotropic gold nanostructures was observed at low concentrations of pectin, while its increase results in the formation of smaller sharp edged perfect triangles with a considerable number of quasi-spherically shaped gold NP. On the other hand, the size of spherical silver NP decreased as the biopolymer concentration in the solution increased. The surface-enhanced Raman scattering enhancement of different NPs was evaluated using a Cu-complex of cationic tetrakis(4-N-methylpyridyl)porphyrin as a probe molecule at 441.6 and 532 nm excitation. Great enhancement of Raman signal was obtained with a pectin-silver NP and for most of them their levels were higher than that for the routinely synthesized citrate silver NP.

  1. Morphological dependence of silver electrodeposits investigated by changing the ionic liquid solvent and the deposition parameters.

    Science.gov (United States)

    Figueredo-Sobrinho, Francisco A A; Santos, Luis P M; Leite, Davi S; Craveiro, Diego C; Santos, Samir H; Eguiluz, Katlin I B; Salazar-Banda, Giancarlo R; Maciel, Cleiton D; Coutinho-Neto, Maurício D; Homem-de-Mello, Paula; de Lima-Neto, Pedro; Correia, Adriana N

    2016-03-14

    The low toxicity and environmentally compatible ionic liquids (ILs) are alternatives to the toxic and harmful cyanide-based baths used in industrial silver electrodeposition. Here, we report the successful galvanostatic electrodeposition of silver films using the air and water stable ILs 1-ethyl-3-methylimidazolium trifluoromethylsulfonate ([EMIM]TfO) and 1-H-3-methylimidazolium hydrogen sulphate ([HMIM(+)][HSO4(-)]) as solvents and AgTfO as the source of silver. The electrochemical deposition parameters were thoughtfully studied by cyclic voltammetry before deposition. The electrodeposits were characterized by scanning electron microscopy coupled with X-ray energy dispersive spectroscopy and X-ray diffraction. Molecular dynamics (MD) simulations were used to investigate the structural dynamic and energetic properties of AgTfO in both ILs. Cyclic voltammetry experiments revealed that the reduction of silver is a diffusion-controlled process. The morphology of the silver coatings obtained in [EMIM]TfO is independent of the applied current density, resulting in nodular electrodeposits grouped as crystalline clusters. However, the current density significantly influences the morphology of silver electrodeposits obtained in [HMIM(+)][HSO4(-)], thus evolving from dendrites at 15 mA cm(-2) to the coexistence of dendrites and columnar shapes at 30 mA cm(-2). These differences are probably due to the greater interaction of Ag(+) with [HSO4(-)] than with TfO(-), as indicated by the MD simulations. The morphology of Ag deposits is independent of the electrodeposition temperature for both ILs, but higher values of temperature promoted increased cluster sizes. Pure face-centred cubic polycrystalline Ag was deposited on the films with crystallite sizes on the nanometre scale. The morphological dependence of Ag electrodeposits obtained in the [HMIM(+)][HSO4(-)] IL on the current density applied opens up the opportunity to produce different and predetermined Ag deposits. PMID

  2. Nano-volcanic Eruption of Silver

    Science.gov (United States)

    Lin, Shih-kang; Nagao, Shijo; Yokoi, Emi; Oh, Chulmin; Zhang, Hao; Liu, Yu-chen; Lin, Shih-guei; Suganuma, Katsuaki

    2016-01-01

    Silver (Ag) is one of the seven metals of antiquity and an important engineering material in the electronic, medical, and chemical industries because of its unique noble and catalytic properties. Ag thin films are extensively used in modern electronics primarily because of their oxidation-resistance. Here we report a novel phenomenon of Ag nano-volcanic eruption that is caused by interactions between Ag and oxygen (O). It involves grain boundary liquation, the ejection of transient Ag-O fluids through grain boundaries, and the decomposition of Ag-O fluids into O2 gas and suspended Ag and Ag2O clusters. Subsequent coating with re-deposited Ag-O and the de-alloying of O yield a conformal amorphous Ag coating. Patterned Ag hillock arrays and direct Ag-to-Ag bonding can be formed by the homogenous crystallization of amorphous coatings. The Ag “nano-volcanic eruption” mechanism is elaborated, shedding light on a new mechanism of hillock formation and new applications of amorphous Ag coatings. PMID:27703220

  3. Nano-volcanic Eruption of Silver

    Science.gov (United States)

    Lin, Shih-Kang; Nagao, Shijo; Yokoi, Emi; Oh, Chulmin; Zhang, Hao; Liu, Yu-Chen; Lin, Shih-Guei; Suganuma, Katsuaki

    2016-10-01

    Silver (Ag) is one of the seven metals of antiquity and an important engineering material in the electronic, medical, and chemical industries because of its unique noble and catalytic properties. Ag thin films are extensively used in modern electronics primarily because of their oxidation-resistance. Here we report a novel phenomenon of Ag nano-volcanic eruption that is caused by interactions between Ag and oxygen (O). It involves grain boundary liquation, the ejection of transient Ag-O fluids through grain boundaries, and the decomposition of Ag-O fluids into O2 gas and suspended Ag and Ag2O clusters. Subsequent coating with re-deposited Ag-O and the de-alloying of O yield a conformal amorphous Ag coating. Patterned Ag hillock arrays and direct Ag-to-Ag bonding can be formed by the homogenous crystallization of amorphous coatings. The Ag “nano-volcanic eruption” mechanism is elaborated, shedding light on a new mechanism of hillock formation and new applications of amorphous Ag coatings.

  4. FY 1997 research and development of fusion domains. Part 1. Studies on cluster science; 1997 nendo seika hokokusho (yugo ryoiki kenkyu kaihatsu). 1. Cluster Science no kenkyu

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1998-03-01

    Studies were made on clusters which are thought to play important roles in status changes in substances (coagulation, crystallization and phase segregation) and chemical reactions (combustion, aqueous solution reaction and catalytic reaction). In the study of clusters by using infrared spectra, a method was developed to detect by using mass analyzer the cluster ion amount produced by dual resonance between resonantly enhanced multiphoton ionization (REMPI) and infrared lights. Fabrication of a Terahertz spectrometer was planned to enable high-resolution and high-accuracy observation on molecular clusters. Clusters consisting of silver atoms and ammonia molecules were successfully observed. A method was developed to investigate size dependence of cluster reactivity by using a Fourier converted ion cyclotron resonant mass analyzer. In addition, studies were conducted on clusters in liquids and aqueous solutions, clusters frozen in surface and matrix, and clusters stabilized in micro-space. 96 refs., 34 figs., 2 tabs.

  5. Single-source precursors for alloyed gold-silver nanocrystals - a molecular metallurgy approach.

    Science.gov (United States)

    Zopes, David; Hegemann, Corinna; Schläfer, Johannes; Tyrra, Wieland; Mathur, Sanjay

    2015-04-20

    Multiple silver(I)-aurates(I) have been prepared by salt metathesis reactions that act as efficient single-source precursors to colloidal gold silver alloys with the highest possible atom economy in the chemical synthesis of nanostructures. The CF3 group present on the Au cation acts as an in situ reducing agent and can be converted into CO ligands by simple hydrolysis. This ligand-mediated activation and subsequent decomposition of metal-organic precursors impose a molecular control over the nucleation process, producing homogeneously alloyed (Ag-Au) nanoparticles with an atomic Au:Ag ratio of 1:1. The concept also works for the Au-Cu system and acts as a pointer to replace Au (Ag) with less expensive (Cu) metals.

  6. Agar hydrogel with silver nanoparticles to prolong the shelf life of Fior di Latte cheese.

    Science.gov (United States)

    Incoronato, A L; Conte, A; Buonocore, G G; Del Nobile, M A

    2011-04-01

    The objective of this work was to evaluate the effectiveness of an antimicrobial packaging system containing active nanoparticles on the quality deterioration of Fior di Latte cheese. To this aim, 3 concentrations of silver montmorillonite embedded in agar were used. The cell loads of spoilage and useful microorganisms were monitored during a refrigerated storage period. Moreover, cheese sensory quality (i.e., odor, color, consistency, and overall quality) was evaluated by means of a panel test. Results showed that the active packaging system markedly increased the shelf life of Fior di Latte cheese, due to the ability of silver cations to control microbial proliferation, without affecting the functional dairy microbiota and the sensory characteristics of the product. The active packaging system developed in this work could be used to prolong the shelf life of Fior di Latte and boost its distribution beyond local market borders.

  7. Aquatic Toxicity Comparison of Silver Nanoparticles and Silver Nanowires.

    Science.gov (United States)

    Sohn, Eun Kyung; Johari, Seyed Ali; Kim, Tae Gyu; Kim, Jin Kwon; Kim, Ellen; Lee, Ji Hyun; Chung, Young Shin; Yu, Il Je

    2015-01-01

    To better understand the potential ecotoxicological impact of silver nanoparticles (AgNPs) and silver nanowires (AgNWs) released into freshwater environments, the toxicities of these nanomaterials were assessed and compared using Organization for Economic Cooperation and Development (OECD) test guidelines, including a "Daphnia sp., acute immobilization test," "Fish, acute toxicity test," and "freshwater alga and cyanobacteria, growth inhibition test." Based on the estimated median lethal/effective concentrations of AgNPs and AgNWs, the susceptibility to the nanomaterials was different among test organisms (daphnia > algae > fish), suggesting that the AgNPs are classified as "category acute 1" for Daphnia magna, "category acute 2" for Oryzias latipes, and "category acute 1" for Raphidocelis subcapitata, while the AgNWs are classified as "category acute 1" for Daphnia magna, "category acute 2" for Oryzias latipes, and "category acute 2" for Raphidocelis subcapitata, according to the GHS (Globally Harmonized System of Classification and Labelling of Chemicals). In conclusion, the present results suggest that more attention should be paid to prevent the accidental or intentional release of silver nanomaterials into freshwater aquatic environments. PMID:26125025

  8. Application of Silver and Silver Oxide Nanoparticles Impregnated on Activated Carbon to the Degradation of Bromate.

    Science.gov (United States)

    Choi, J S; Lee, H; Park, Y K; Kim, S J; Kim, B J; An, K H; Kim, B H; Jung, S C

    2016-05-01

    Silver and silver oxide nanoparticles were impregnated on the surface of powdered activated carbon (PAC) using a single-step liquid phase plasma (LPP) method. Spherical silver and silver oxide nanoparticles of 20 to 100 nm size were dipersed evenly on the surface of PAC. The impregnated PAC exhibited a higher activity for the decomposition of bromate than bare PAC. The XPS, Raman and EDX analyses showed that the Ag/PAC composites synthesized by the LPP process. PMID:27483780

  9. Polyamide/silver antimicrobials: Effect of filler types on the silver ion release

    OpenAIRE

    Kumar, Radhesh; Howdle, Steve; Münstedt, Helmut

    2005-01-01

    Abstract: The efficiency of various silver-based antimicrobial fillers (elementary silver and silver substituted materials) in polyamide (PA) toward their silver ion (Ag�) release characteristics in an aqueous medium was investigated and discussed. Anode stripping voltammetry (ASV) was used for the quantitative estimation of Ag� release from these composites. The biocidal (Ag�) release from the composites was found to be dependent on the time of soaking in water and the nature ...

  10. Silver nanocluster catalytic microreactors for water purification

    Science.gov (United States)

    Da Silva, B.; Habibi, M.; Ognier, S.; Schelcher, G.; Mostafavi-Amjad, J.; Khalesifard, H. R. M.; Tatoulian, M.; Bonn, D.

    2016-07-01

    A new method for the elaboration of a novel type of catalytic microsystem with a high specific area catalyst is developed. A silver nanocluster catalytic microreactor was elaborated by doping a soda-lime glass with a silver salt. By applying a high power laser beam to the glass, silver nanoclusters are obtained at one of the surfaces which were characterized by BET measurements and AFM. A microfluidic chip was obtained by sealing the silver coated glass with a NOA 81 microchannel. The catalytic activity of the silver nanoclusters was then tested for the efficiency of water purification by using catalytic ozonation to oxidize an organic pollutant. The silver nanoclusters were found to be very stable in the microreactor and efficiently oxidized the pollutant, in spite of the very short residence times in the microchannel. This opens the way to study catalytic reactions in microchannels without the need of introducing the catalyst as a powder or manufacturing complex packed bed microreactors.

  11. Preparation of silver nanoparticles at low temperature

    Science.gov (United States)

    Mishra, Mini; Chauhan, Pratima

    2016-04-01

    Silver from ancient time is used as antimicrobial agent in the bulk form but now with the advancement in nanotechnology silver in the form of nanoparticles shown potential effect against microbes which make us easy to fight with many diseases plants and animals. In this work silver nanoparticles were synthesized by chemical routes using sodium borohydride as reducing agent at low temperature. The particles were characterized through UV-Visible spectroscopy as well as X-Ray Diffraction. The UV-visible spectra of silver nanoparticles exhibited absorption at 425 cm; the crystallite size of the particles is between 19nm to 39nm. EDAX graph shows two peaks of silver and oxygen. Water absorbed by silver nanoparticles was removed by the calcinations.

  12. Risk assessment of silver nanoparticles

    Science.gov (United States)

    Shipelin, V. A.; Gmoshinski, I. V.; Khotimchenko, S. A.

    2015-11-01

    Nanoparticles of metallic silver (Ag) are among the most widely used products of nanotechnology. Nanosized colloidal silver (NCS) is presented in many kinds of production as solutions of particles with diameter less than 100 nm. NCS is used in a variety of fields, including food supplements, medicines, cosmetics, packaging materials, disinfectants, water filters, and many others. Problems of toxicity and related safety of NCS for humans and environmental systems are recently overestimated basing on data of numerous toxicological studies in vitro and in vivo. The article discusses the results of current studies in recent years and the data of author's own experiments on studying the safety of NCS, that allows to move on to risk assessment of this nanomaterial presented in consumer products and environmental samples.

  13. Fluorescent Thiol-Derivatized Gold Clusters Embedded in Polymers

    Directory of Open Access Journals (Sweden)

    G. Carotenuto

    2013-01-01

    Full Text Available Owing to aurophilic interactions, linear and/or planar Au(I-thiolate molecules spontaneously aggregate, leading to molecular gold clusters passivated by a thiolate monolayer coating. Differently from the thiolate precursors, such cluster compounds show very intensive visible fluorescence characteristics that can be tuned by alloying the gold clusters with silver atoms or by conjugating the electronic structure of the metallic core with unsaturated electronic structures in the organic ligand through the sulphur atom. Here, the photoluminescence features of some examples of these systems are shortly described.

  14. Atomistic Potentials for Palladium-Silver Hydrides

    OpenAIRE

    Hale, L. M.; Wong, B. M.; Zimmerman, J. A.; Zhou, X.

    2013-01-01

    New EAM potentials for the ternary palladium-silver-hydrogen system are developed by extending a previously developed palladium-hydrogen potential. The ternary potentials accurately capture the heat of mixing and structural properties associated with solid solution alloys of palladium-silver. Stable hydrides are produced with properties that smoothly transition across the compositions. Additions of silver to palladium are predicted to alter the properties of the hydrides by decreasing the mis...

  15. Silver staining of proteins in polyacrylamide gels

    OpenAIRE

    Chevallet, Mireille; Luche, Sylvie; Rabilloud, Thierry

    2006-01-01

    International audience Silver staining is used to detect proteins after electrophoretic separation on polyacrylamide gels. It combines excellent sensitivity (in the low nanogram range) with the use of very simple and cheap equipment and chemicals. It is compatible with downstream processing, such as mass spectrometry analysis after protein digestion. The sequential phases of silver staining are protein fixation, then sensitization, then silver impregnation and finally image development. Se...

  16. Synthesis and optical properties of silver nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Singh, Jaiveer [Department of Physics, ISLE, IPS Academy, Rajendra Nagar, Indore 452012, MP (India); Kaurav, Netram, E-mail: netramkaurav@yahoo.co.uk [Department of Physics, Holkar Science College, A-B Road, Indore 452001 (India); Choudhary, K. K. [Department of Physics, National Defence Academy, Khadakwasala, Pune -411023 (India); Okram, Gunadhor S. [Electrical Transport Laboratory, UGC-DAR Consortium for Scientific Research, University Campus, Khandwa Road, Indore-452001 (India)

    2015-07-31

    The preparation of stable, uniform silver nanoparticles by reduction of silver acetate by ethylene glycol (EG) is reported in the present paper. It is a simple process of recent interest for obtaining silver nanoparticles. The samples were characterized by X-Ray diffraction (XRD), which reveals an average particle size (D) of 38 nm. The UV/Vis spectra show that an absorption peak, occurring due to surface plasmon resonance (SPR), exists at 319 nm.

  17. Cation locations and dislocations in zeolites

    Science.gov (United States)

    Smith, Luis James

    The focus of this dissertation is the extra-framework cation sites in a particular structural family of zeolites, chabazite. Cation sites play a particularly important role in the application of these sieves for ion exchange, gas separation, catalysis, and, when the cation is a proton, acid catalysis. Structural characterization is commonly performed through the use of powder diffraction and Rietveld analysis of powder diffraction data. Use of high-resolution nuclear magnetic resonance, in the study of the local order of the various constituent nuclei of zeolites, complements well the long-range order information produced by diffraction. Recent developments in solid state NMR techniques allow for increased study of disorder in zeolites particularly when such phenomena test the detection limits of diffraction. These two powerful characterization techniques, powder diffraction and NMR, offer many insights into the complex interaction of cations with the zeolite framework. The acids site locations in SSZ-13, a high silica chabazite, and SAPO-34, a silicoaluminophosphate with the chabazite structure, were determined. The structure of SAPO-34 upon selective hydration was also determined. The insensitivity of X-rays to hydrogen was avoided through deuteration of the acid zeolites and neutron powder diffraction methods. Protons at inequivalent positions were found to have different acid strengths in both SSZ-13 and SAPO-34. Other light elements are incorporated into zeolites in the form of extra-framework cations, among these are lithium, sodium, and calcium. Not amenable by X-ray powder diffraction methods, the positions of such light cations in fully ion-exchanged versions of synthetic chabazite were determined through neutron powder diffraction methods. The study of more complex binary cation systems were conducted. Powder diffraction and solid state NMR methods (MAS, MQMAS) were used to examine cation site preferences and dislocations in these mixed-akali chabazites

  18. Organic non-aqueous cation-based redox flow batteries

    Energy Technology Data Exchange (ETDEWEB)

    Jansen, Andrew N.; Vaughey, John T.; Chen, Zonghai; Zhang, Lu; Brushett, Fikile R.

    2016-03-29

    The present invention provides a non-aqueous redox flow battery comprising a negative electrode immersed in a non-aqueous liquid negative electrolyte, a positive electrode immersed in a non-aqueous liquid positive electrolyte, and a cation-permeable separator (e.g., a porous membrane, film, sheet, or panel) between the negative electrolyte from the positive electrolyte. During charging and discharging, the electrolytes are circulated over their respective electrodes. The electrolytes each comprise an electrolyte salt (e.g., a lithium or sodium salt), a transition-metal free redox reactant, and optionally an electrochemically stable organic solvent. Each redox reactant is selected from an organic compound comprising a conjugated unsaturated moiety, a boron cluster compound, and a combination thereof. The organic redox reactant of the positive electrolyte is selected to have a higher redox potential than the redox reactant of the negative electrolyte.

  19. Cycloaliphatic epoxide resins for cationic UV - cure

    International Nuclear Information System (INIS)

    This paper introduces the cyclo - aliphatic epoxide resins used for the various applications of radiation curing and their comparison with acrylate chemistry. Radiation curable coatings and inks are pre - dominantly based on acrylate chemistry but over the last few years, cationic chemistry has emerged successfully with the unique properties inherent with cyclo - aliphatic epoxide ring structures. Wide variety of cationic resins and diluents, the formulation techniques to achieve the desired properties greatly contributes to the advancement of UV - curing technology

  20. Cations and activated sludge floc structure

    OpenAIRE

    Park, Chul

    2002-01-01

    This research was designed to investigate the effect of cations on activated sludge characteristics and also to determine their influence on digestion performance. For this purpose, cations in solution and in floc were evaluated along with various activated sludge characteristics and the collected waste activated sludge underwent both anaerobic and aerobic digestion. It was found that large amounts of biopolymer (protein + polysaccharide) remained in the effluent of WWTP that received high in...

  1. Test procedure for cation exchange chromatography

    International Nuclear Information System (INIS)

    The purpose of this test plan is to demonstrate the synthesis of inorganic antimonate ion exchangers and compare their performance against the standard organic cation exchangers. Of particular interest is the degradation rate of both inorganic and organic cation exchangers. This degradation rate will be tracked by determining the ion exchange capacity and thermal stability as a function of time, radiation dose, and chemical reaction

  2. Silica-based cationic bilayers as immunoadjuvants

    OpenAIRE

    Carmona-Ribeiro Ana M; da Costa Maria; Faquim-Mauro Eliana; Santana Mariana RA; Lincopan Nilton

    2009-01-01

    Abstract Background Silica particles cationized by dioctadecyldimethylammonium bromide (DODAB) bilayer were previously described. This work shows the efficiency of these particulates for antigen adsorption and presentation to the immune system and proves the concept that silica-based cationic bilayers exhibit better performance than alum regarding colloid stability and cellular immune responses for vaccine design. Results Firstly, the silica/DODAB assembly was characterized at 1 mM NaCl, pH 6...

  3. Structural Insights into Mitochondrial Calcium Uniporter Regulation by Divalent Cations.

    Science.gov (United States)

    Lee, Samuel K; Shanmughapriya, Santhanam; Mok, Mac C Y; Dong, Zhiwei; Tomar, Dhanendra; Carvalho, Edmund; Rajan, Sudarsan; Junop, Murray S; Madesh, Muniswamy; Stathopulos, Peter B

    2016-09-22

    Calcium (Ca(2+)) flux into the matrix is tightly controlled by the mitochondrial Ca(2+) uniporter (MCU) due to vital roles in cell death and bioenergetics. However, the precise atomic mechanisms of MCU regulation remain unclear. Here, we solved the crystal structure of the N-terminal matrix domain of human MCU, revealing a β-grasp-like fold with a cluster of negatively charged residues that interacts with divalent cations. Binding of Ca(2+) or Mg(2+) destabilizes and shifts the self-association equilibrium of the domain toward monomer. Mutational disruption of the acidic face weakens oligomerization of the isolated matrix domain and full-length human protein similar to cation binding and markedly decreases MCU activity. Moreover, mitochondrial Mg(2+) loading or blockade of mitochondrial Ca(2+) extrusion suppresses MCU Ca(2+)-uptake rates. Collectively, our data reveal that the β-grasp-like matrix region harbors an MCU-regulating acidic patch that inhibits human MCU activity in response to Mg(2+) and Ca(2+) binding.

  4. Microwave assisted template synthesis of silver nanoparticles

    Indian Academy of Sciences (India)

    K J Sreeram; M Nidhin; B U Nair

    2008-12-01

    Easier, less time consuming, green processes, which yield silver nanoparticles of uniform size, shape and morphology are of interest. Various methods for synthesis, such as conventional temperature assisted process, controlled reaction at elevated temperatures, and microwave assisted process have been evaluated for the kind of silver nanoparticles synthesized. Starch has been employed as a template and reducing agent. Electron microscopy, photon correlation spectroscopy and surface plasmon resonance have been employed to characterize the silver nanoparticles synthesized. Compared to conventional methods, microwave assisted synthesis was faster and provided particles with an average particle size of 12 nm. Further, the starch functions as template, preventing the aggregation of silver nanoparticles.

  5. Morphology of a silver/polyacrylonitrile nanocomposite

    Science.gov (United States)

    Kudryashov, M. A.; Mashin, A. I.; Tyurin, A. S.; Fedosov, A. E.; Chidichimo, G.; De Filpo, G.

    2011-01-01

    Silver/polyacrylonitrile (Ag/PAN) nanocomposites are synthesized at the stage of simultaneous acrylonitrile polymerization and the reduction of silver ions from a mixture of silver nitrate AgNO3, acrylonitrile, and a photoinitiator. The synthesized films are transparent in the visible region and are characterized by a uniform dispersion of silver nanoparticles in a PAN matrix without any macroscopic agglomeration. The effects of the metal salt and photoinitiator concentrations on the size and density of metal nanoparticles in a composite are revealed.

  6. Cluster headache

    Science.gov (United States)

    Doctors do not know exactly what causes cluster headaches. They seem to be related to the body's sudden release of histamine (chemical in the body released during an allergic response) or serotonin (chemical made by nerve cells). A problem in a small area at ...

  7. Photoelectron velocity-map imaging signature of structural evolution of silver-doped lead Zintl anions.

    Science.gov (United States)

    Xie, Hua; Qin, Zhengbo; Wu, Xia; Tang, Zichao; Jiang, Ling

    2012-08-14

    A set of silver-doped lead Zintl anions, Ag@Pb(n)(-) (n = 5-12), have been studied using photoelectron velocity-map imaging spectroscopy and quantum chemical calculation. The structures of Ag@Pb(n)(-) (n = 7-9, 11) built upon a square pyramid base, hitherto not considered, were assigned. Overall agreement between the experimental and calculated photoelectron spectra as well as vertical detachment energies allows for structural evolution to be established. The silver atom prefers to stay outside in the n ≤ 6 clusters and intends to be encapsulated by the lead atoms in n > 6. A stable endohedral cage with bicapped square antiprism structure is formed at n = 10, the endohedral structure of which persists for the larger clusters. Especially, these Ag@Pb(n)(-) anions have been found to undergo a transition between square pyramid and pentagonal pyramid molecular structures at n = 11. PMID:22897284

  8. Synthesis and Characterization of Optically Active Fractal Seed Mediated Silver Nickel Bimetallic Nanoparticles

    Directory of Open Access Journals (Sweden)

    Joseph Adeyemi Adekoya

    2014-01-01

    Full Text Available The synthesis of new seed mediated AgNi allied bimetallic nanocomposites was successfully carried out by the successive reduction of the metal ions in diethylene glycol, ethylene glycol, glycerol, and pentaerythritol solutions, with concomitant precipitation of Ag/Ni bimetal sols. The optical measurement revealed the existence of distinct band edge with surface plasmon resonance (SPR in the region of 400–425 nm and excitonic emission with maximum peak at 382 nm which were reminiscent of cluster-in-cluster surface enriched bimetallic silver-nickel sols. The morphological characterization by transmission electron microscopy, high resolution transmission electron microscopy, and X-ray diffraction analyses complimented by surface scan using X-ray photoelectron spectroscopy strongly supported the formation of intimately alloyed face-centered silver/nickel nanoclusters.

  9. Dilution thermodynamics of the biologically relevant cation mixtures

    Energy Technology Data Exchange (ETDEWEB)

    Kaczyński, Marek, E-mail: marek.kaczynski@pwr.wroc.pl; Borowik, Tomasz, E-mail: office@novel-id.pl; Przybyło, Magda, E-mail: magdalena.przybylo@pwr.wroc.pl; Langner, Marek, E-mail: marek.langner@pwr.wroc.pl

    2014-01-10

    Graphical abstract: - Highlights: • Dilution energetics of Ca{sup 2+} can be altered by the aqueous phase ionic composition. • Dissipated heat upon Ca{sup 2+} dilution is drastically reduced in the K{sup +} presence. • Reduction of the enthalpy change upon Ca{sup 2+} dilution is K{sup +} concentration dependent. • The cooperativity of Ca{sup 2+} hydration might be of great biological relevance providing a thermodynamic argument for the specific ionic composition of the intracellular environment. - Abstract: The ionic composition of intracellular space is rigorously controlled by a variety of processes consuming large quantities of energy. Since the energetic efficiency is an important evolutional criterion, therefore the ion fluxes within the cell should be optimized with respect to the accompanying energy consumption. In the paper we present the experimental evidence that the dilution enthalpies of the biologically relevant ions; i.e. calcium and magnesium depend on the presence of monovalent cations; i.e. sodium and potassium. The heat flow generated during the dilution of ionic mixtures was measured with the isothermal titration calorimetry. When calcium was diluted together with potassium the dilution enthalpy was drastically reduced as the function of the potassium concentration present in the solution. No such effect was observed when the potassium ions were substituted with sodium ones. When the dilution of magnesium was investigated the dependence of the dilution enthalpy on the accompanying monovalent cation was much weaker. In order to interpret experimental evidences the ionic cluster formation is postulated. The specific organization of such cluster should depend on ions charges, sizes and organization of the hydration layers.

  10. Selective extraction of copper, mercury, silver and palladium ionsfrom water using hydrophobic ionic liquids.

    Energy Technology Data Exchange (ETDEWEB)

    Papaiconomou, Nicolas; Lee, Jong-Min; Salminen, Justin; VonStosch, Moritz; Prausnitz, John M.

    2007-06-25

    Extraction of dilute metal ions from water was performed near room temperature with a variety of ionic liquids. Distribution coefficients are reported for fourteen metal ions extracted with ionic liquids containing cations 1-octyl-4-methylpyridinium [4MOPYR]{sup +}, 1-methyl-1-octylpyrrolidinium [MOPYRRO]{sup +} or 1-methyl-1-octylpiperidinium [MOPIP]{sup +}, and anions tetrafluoroborate [BF{sub 4}]{sup +}, trifluoromethyl sulfonate [TfO]{sup +} or nonafluorobutyl sulfonate [NfO]{sup +}. Ionic liquids containing octylpyridinium cations are very good for extracting mercury ions. However, other metal ions were not significantly extracted by any of these ionic liquids. Extractions were also performed with four new task-specific ionic liquids. Such liquids containing a disulfide functional group are efficient and selective for mercury and copper, whereas those containing a nitrile functional group are efficient and selective for silver and palladium.

  11. Selective extraction of copper, mercury, silver and palladium ions from water using hydrophobic ionic liquids

    International Nuclear Information System (INIS)

    Extraction of dilute metal ions from water was performed near room temperature with a variety of ionic liquids. Distribution coefficients are reported for fourteen metal ions extracted with ionic liquids containing cations 1-octyl-4-methylpyridinium [4MOPYR]+, 1-methyl-1-octylpyrrolidinium [MOPYRRO]+ or 1-methyl-1-octylpiperidinium [MOPIP]+, and anions tetrafluoroborate [BF4]+, trifluoromethyl sulfonate [TfO]+ or nonafluorobutyl sulfonate [NfO]+. Ionic liquids containing octylpyridinium cations are very good for extracting mercury ions. However, other metal ions were not significantly extracted by any of these ionic liquids. Extractions were also performed with four new task-specific ionic liquids. Such liquids containing a disulfide functional group are efficient and selective for mercury and copper, whereas those containing a nitrile functional group are efficient and selective for silver and palladium

  12. Synthesis and antimicrobial effects of silver nanoparticles

    Directory of Open Access Journals (Sweden)

    S kheybari

    2010-09-01

    Full Text Available "n  "n "nBackground and the purpose of the study:The most prominent nanoparticles for medical uses are nanosilver particles which are famous for their high anti-microbial activity. Silver ion has been known as a metal ion that exhibit anti-mold, anti-microbial and anti-algal properties for a long time. In particular, it is widely used as silver nitrate aqueous solution which has disinfecting and sterilizing actions. The purpose of this study was to evaluate the antimicrobial activity as well as physical properties of the silver nanoparticles prepared by chemical reduction method. "nMethods:Silver nanoparticles (NPs were prepared by reduction of silver nitrate in the presence of a reducing agent and also poly [N-vinylpyrolidone] (PVP as a stabilizer. Two kinds of NPs were synthesized by ethylene glycol (EG and glucose as reducing agent. The nanostructure and particle size of silver NPs were confirmed by scanning electron microscopy (SEM and laser particle analyzer (LPA. The formations of the silver NPs were monitored using ultraviolet-visible spectroscopy. The anti-bacterial activity of silver NPs were assessed by determination of their minimum inhibitory concentrations (MIC against the Gram positive (Staphylococcus aureus and Staphylococcus epidermidis as well as Gram-negative (Escherichia coli and Pseudomonas aeruginosa bacteria. "nResults and Conclusion:The silver nanoparticles were spherical with particle size between 10 to 250 nm. Analysis of the theoretical (Mie light scattering theory and experimental results showed that the silver NPs in colloidal solution had a diameter of approximately 50 nm. "nBoth colloidal silver NPs showed high anti-bacterial activity against Gram positive and Gram negative bacteria. Glucose nanosilver colloids showed a shorter killing time against most of the tested bacteria which could be due to their nanostructures and uniform size distribution patterns.

  13. Regional Innovation Clusters

    Data.gov (United States)

    Small Business Administration — The Regional Innovation Clusters serve a diverse group of sectors and geographies. Three of the initial pilot clusters, termed Advanced Defense Technology clusters,...

  14. Distribution of silver in rats following 28 days of repeated oral exposure to silver nanoparticles or silver acetate

    Directory of Open Access Journals (Sweden)

    Mortensen Alicja

    2011-06-01

    Full Text Available Abstract Background The study investigated the distribution of silver after 28 days repeated oral administration of silver nanoparticles (AgNPs and silver acetate (AgAc to rats. Oral administration is a relevant route of exposure because of the use of silver nanoparticles in products related to food and food contact materials. Results AgNPs were synthesized with a size distribution of 14 ± 4 nm in diameter (90% of the nanoparticle volume and stabilized in aqueous suspension by the polymer polyvinylpyrrolidone (PVP. The AgNPs remained stable throughout the duration of the 28-day oral toxicity study in rats. The organ distribution pattern of silver following administration of AgNPs and AgAc was similar. However the absolute silver concentrations in tissues were lower following oral exposure to AgNPs. This was in agreement with an indication of a higher fecal excretion following administration of AgNPs. Besides the intestinal system, the largest silver concentrations were detected in the liver and kidneys. Silver was also found in the lungs and brain. Autometallographic (AMG staining revealed a similar cellular localization of silver in ileum, liver, and kidney tissue in rats exposed to AgNPs or AgAc. Using transmission electron microscopy (TEM, nanosized granules were detected in the ileum of animals exposed to AgNPs or AgAc and were mainly located in the basal lamina of the ileal epithelium and in lysosomes of macrophages within the lamina propria. Using energy dispersive x-ray spectroscopy it was shown that the granules in lysosomes consisted of silver, selenium, and sulfur for both AgNP and AgAc exposed rats. The diameter of the deposited granules was in the same size range as that of the administered AgNPs. No silver granules were detected by TEM in the liver. Conclusions The results of the present study demonstrate that the organ distribution of silver was similar when AgNPs or AgAc were administered orally to rats. The presence of silver

  15. Antibacterial activities of silver nanoparticles and antibiotic-adsorbed silver nanoparticles against biorecycling microbes.

    Science.gov (United States)

    Khurana, Chandni; Vala, Anjana K; Andhariya, Nidhi; Pandey, O P; Chudasama, Bhupendra

    2014-09-20

    Silver nanoparticles have a huge share in nanotechnology based products used in clinical and hygiene products. Silver nanoparticles leaching from these medical and domestic products will eventually enter terrestrial ecosystems and will interact with the microbes present in the land and water. These interactions could be a threat to biorecycling microbes present in the Earth's crust. The antimicrobial action towards biorecycling microbes by leached silver nanoparticles from medical waste could be many times greater compared to that of silver nanoparticles leached from other domestic products, since medical products may contain traditional antibiotics along with silver nanoparticles. In the present article, we have evaluated the antimicrobial activities of as-synthesized silver nanoparticles, antibiotics - tetracycline and kanamycin, and antibiotic-adsorbed silver nanoparticles. The antimicrobial action of silver nanoparticles with adsorbed antibiotics is 33-100% more profound against the biorecycling microbes B. subtilis and Pseudomonas compared to the antibacterial action of silver nanoparticles of the same concentration. This study indicates that there is an immediate and urgent need for well-defined protocols for environmental exposure to silver nanoparticles, as the use of silver nanoparticles in nanotechnology based products is poorly restricted.

  16. Toxicity of various silver nanoparticles compared to silver ions in Daphnia magna

    Directory of Open Access Journals (Sweden)

    Asghari Saba

    2012-04-01

    Full Text Available Abstract Background To better understand the potential ecotoxicological impacts of silver nanoparticles released into freshwater environments, the Daphnia magna 48-hour immobilization test was used. Methods The toxicities of silver nitrate, two types of colloidal silver nanoparticles, and a suspension of silver nanoparticles were assessed and compared using standard OECD guidelines. Also, the swimming behavior and visible uptake of the nanoparticles by Daphnia were investigated and compared. The particle suspension and colloids used in the toxicity tests were well-characterized. Results The results obtained from the exposure studies showed that the toxicity of all the silver species tested was dose and composition dependent. Plus, the silver nanoparticle powders subsequently suspended in the exposure water were much less toxic than the previously prepared silver nanoparticle colloids, whereas the colloidal silver nanoparticles and AgNO3 were almost similar in terms of mortality. The silver nanoparticles were ingested by the Daphnia and accumulated under the carapace, on the external body surface, and connected to the appendages. All the silver species in this study caused abnormal swimming by the D. magna. Conclusion According to the present results, silver nanoparticles should be classified according to GHS (Globally Harmonized System of classification and labeling of chemicals as "category acute 1" to Daphnia neonates, suggesting that the release of nanosilver into the environment should be carefully considered.

  17. Glass frits coated with silver nanoparticles for silicon solar cells

    Science.gov (United States)

    Li, Yingfen; Gan, Weiping; Zhou, Jian; Li, Biyuan

    2015-06-01

    Glass frits coated with silver nanoparticles were prepared by electroless plating. Gum Arabic (GA) was used as the activating agent of glass frits without the assistance of stannous chloride or palladium chloride. The silver-coated glass frits prepared with different GA dosages were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), and thermogravimetric analysis (TGA). The characterization results indicated that silver-coated glass frits had the structures of both glass and silver. Spherical silver nanoparticles were distributed on the glass frits evenly. The density and particle size of silver nanoparticles on the glass frits can be controlled by adjusting the GA dosage. The silver-coated glass frits were applied to silver pastes to act as both the densification promoter and silver crystallite formation aid in the silver electrodes. The prepared silver-coated glass frits can improve the photovoltaic performances of solar cells.

  18. Development of nanostructured silver vanadates decorated with silver nanoparticles as a novel antibacterial agent

    Science.gov (United States)

    Holtz, R. D.; Souza Filho, A. G.; Brocchi, M.; Martins, D.; Durán, N.; Alves, O. L.

    2010-05-01

    In this work we report the synthesis, characterization and application of silver vanadate nanowires decorated with silver nanoparticles as a novel antibacterial agent. These hybrid materials were synthesized by a precipitation reaction of ammonium vanadate and silver nitrate followed by hydrothermal treatment. The silver vanadate nanowires have lengths of the order of microns and diameters around 60 nm. The silver nanoparticles decorating the nanowires present a diameter distribution varying from 1 to 20 nm. The influence of the pH of the reaction medium on the chemical structure and morphology of silver vanadates was studied and we found that synthesis performed at pH 5.5-6.0 led to silver vanadate nanowires with a higher morphological yield. The antimicrobial activity of these materials was evaluated against three strains of Staphylococcus aureus and very promising results were found. The minimum growth inhibiting concentration value against a MRSA strain was found to be ten folds lower than for the antibiotic oxacillin.

  19. Development of nanostructured silver vanadates decorated with silver nanoparticles as a novel antibacterial agent

    Energy Technology Data Exchange (ETDEWEB)

    Holtz, R D; Souza Filho, A G; Alves, O L [Laboratorio de Quimica do Estado Solido (LQES), Instituto de Quimica, Universidade Estadual de Campinas, CP 6154, 13081-970, Campinas-SP (Brazil); Brocchi, M; Martins, D [Departamento de Genetica, Evolucao and Bioagentes, Instituto de Biologia, Universidade Estadual de Campinas, Campinas-SP (Brazil); Duran, N, E-mail: rholtz@iqm.unicamp.br, E-mail: agsf@fisica.ufc.br, E-mail: oalves@iqm.unicamp.br [Laboratorio de Quimica Biologica, Instituto de Quimica, Universidade Estadual de Campinas, Campinas-SP (Brazil)

    2010-05-07

    In this work we report the synthesis, characterization and application of silver vanadate nanowires decorated with silver nanoparticles as a novel antibacterial agent. These hybrid materials were synthesized by a precipitation reaction of ammonium vanadate and silver nitrate followed by hydrothermal treatment. The silver vanadate nanowires have lengths of the order of microns and diameters around 60 nm. The silver nanoparticles decorating the nanowires present a diameter distribution varying from 1 to 20 nm. The influence of the pH of the reaction medium on the chemical structure and morphology of silver vanadates was studied and we found that synthesis performed at pH 5.5-6.0 led to silver vanadate nanowires with a higher morphological yield. The antimicrobial activity of these materials was evaluated against three strains of Staphylococcus aureus and very promising results were found. The minimum growth inhibiting concentration value against a MRSA strain was found to be ten folds lower than for the antibiotic oxacillin.

  20. Development of nanostructured silver vanadates decorated with silver nanoparticles as a novel antibacterial agent

    International Nuclear Information System (INIS)

    In this work we report the synthesis, characterization and application of silver vanadate nanowires decorated with silver nanoparticles as a novel antibacterial agent. These hybrid materials were synthesized by a precipitation reaction of ammonium vanadate and silver nitrate followed by hydrothermal treatment. The silver vanadate nanowires have lengths of the order of microns and diameters around 60 nm. The silver nanoparticles decorating the nanowires present a diameter distribution varying from 1 to 20 nm. The influence of the pH of the reaction medium on the chemical structure and morphology of silver vanadates was studied and we found that synthesis performed at pH 5.5-6.0 led to silver vanadate nanowires with a higher morphological yield. The antimicrobial activity of these materials was evaluated against three strains of Staphylococcus aureus and very promising results were found. The minimum growth inhibiting concentration value against a MRSA strain was found to be ten folds lower than for the antibiotic oxacillin.

  1. Cluster forcing

    DEFF Research Database (Denmark)

    Christensen, Thomas Budde

    The cluster theory attributed to Michael Porter has significantly influenced industrial policies in countries across Europe and North America since the beginning of the 1990s. Institutions such as the EU, OECD and the World Bank and governments in countries such as the UK, France, The Netherlands......, Portugal and New Zealand have adopted the concept. Public sector interventions that aim to support cluster development in industries most often focus upon economic policy goals such as enhanced employment and improved productivity, but rarely emphasise broader societal policy goals relating to e...... a difference in terms of enhancing regional development but the paper also concludes that the interventions tend to follow the development path of the established industry and thus tend to neglect long term sustainable development issues while failing to escape the traditional confines of regional industrial...

  2. Silver ion recognition using potentiometric sensor based on recently synthesized isoquinoline-1,3-dione derivatives

    Directory of Open Access Journals (Sweden)

    AJAR KAMAL

    2012-08-01

    Full Text Available The four derivatives of isoquinoline-1,3-dione based on β-lactum (I-IV, have been explored as neutral ionophores for preparing poly(vinylchloride based polymeric membrane electrodes (PME selective to silver(I ions. The addition of sodium tetraphenylborate (NaTPB and dioctylsebacate (DOS as a plasticizer was found to improve the performance of ion selective electrodes. The best performance was obtained with PME-1 based on ionophore I having composition: ionophore (9.2 mg, PVC (100.1 mg, DOS (201.1 mg and NaTPB (1.5 mg in 5 mL tetrahydrofuran. The electrode response was linear with Nernstian slope of 58.44 mV/decade in the concentration range of 1.0 x 10-1 M to 5.0 x 10-6 M and detection limit of 5.83 x 10-6 M. It performs satisfactorily over wide pH range of 1.0-5.5. The proposed sensor can be used over a period of more than three months without any significant drift in potential and shows good selectivity to silver(I ion over a number of cations especially with no interference of mercury(II ions. Sharp end point was obtained when the sensor was used as an indicator electrode for the potentiometric titration of silver(I ions with chloride ions and therefore this electrode (PME-1 could be used for quantitative determination of silver(I ion in synthetic water, silver foil and dental amalgam samples.

  3. Sensor for Silver(I Ion Based on Schiff-base-p-tertbutylcalix[4]arene

    Directory of Open Access Journals (Sweden)

    M. Kumar

    2002-10-01

    Full Text Available The preparation of polymer membrane selective to silver ion and its application to ion-selective electrode is reported here. PVC membrane contain silver-selective calix[4]arene derivative as ionophore. The membrane electrode is highly selective to silver ion and exhibit good linear response over a wide concentration range of 1.0×10-1 to 1.0×10-5M AgNO3 with Nernstian slope of 58.9 mV per decade. The detection limit of electrode is 6.31×10-6 M .The calix[4]arene based membrane electrode exhibit enhanced selectivities for silver ion over other cations; log KPotAg,Na = -2.35, log KPotAg,K= -2.65, log KPotAg,Mg = -4.57, log KPotAg,Ba = -4.10, log KPotAg,Cd = -3.42, log KPotAg,Pb = -3.45.Even the strongest interferent Hg2+ do not interfere to great extent, log KPotAg,Hg = -2.0.The electrode response is stable over wide pH range of 1.0-6.0. The response time of the sensor is 30 seconds and the membrane can be used for more than 6 months without observing any divergence. The sensor can also be applied as an indicator electrode for potentiometric titration of Ag+ ions with Cl-. It is possible to determine Ag(I in the natural water spiked with silver with this electrode assembly.

  4. Clustering experiments

    CERN Document Server

    Wang, Zhengwei; Tan, Ken; Di, Zengru; Roehner, Bertrand M

    2011-01-01

    It is well known that bees cluster together in cold weather, in the process of swarming (when the ``old'' queen leaves with part of the colony) or absconding (when the queen leaves with all the colony) and in defense against intruders such as wasps or hornets. In this paper we describe a fairly different clustering process which occurs at any temperature and independently of any special stimulus or circumstance. As a matter of fact, this process is about four times faster at 28 degree Celsius than at 15 degrees. Because of its simplicity and low level of ``noise'' we think that this phenomenon can provide a means for exploring the strength of inter-individual attraction between bees or other living organisms. For instance, and at first sight fairly surprisingly, our observations showed that this attraction does also exist between bees belonging to different colonies. As this study is aimed at providing a comparative perspective, we also describe a similar clustering experiment for red fire ants.

  5. The Silver Export Quota for 2005

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    <正>China’s Ministry of Commerce recently announced the first lot of silver export quota for 2005. According to report, the first lot of silver export quota amounts to 2,443 tons which is 252 tons more on 2004 basis. There are 37 en-

  6. Intravesical silver nitrate for refractory hemorrhagic cystitis

    Science.gov (United States)

    Montgomery, Brian D.; Boorjian, Stephen A.; Ziegelmann, Matthew J.; Joyce, Daniel D.; Linder, Brian J.

    2016-01-01

    Objective Hemorrhagic cystitis is a challenging clinical entity with limited evidence available to guide treatment. The use of intravesical silver nitrate has been reported, though supporting literature is sparse. Here, we sought to assess outcomes of patients treated with intravesical silver nitrate for refractory hemorrhagic cystitis. Material and methods We identified nine patients with refractory hemorrhagic cystitis treated at our institution with intravesical silver nitrate between 2000–2015. All patients had failed previous continuous bladder irrigation with normal saline and clot evacuation. Treatment success was defined as requiring no additional therapy beyond normal saline irrigation after silver nitrate instillation prior to hospital discharge. Results Median patient age was 80 years (IQR 73, 82). Radiation was the most common etiology for hemorrhagic cystitis 89% (8/9). Two patients underwent high dose (0.1%–0.4%) silver nitrate under anesthesia, while the remaining seven were treated with doses from 0.01% to 0.1% via continuous bladder irrigation for a median of 3 days (range 2–4). All nine patients (100%) had persistent hematuria despite intravesical silver nitrate therapy, requiring additional interventions and red blood cell transfusion during the hospitalization. There were no identified complications related to intravesical silver nitrate instillation. Conclusion Although well tolerated, we found that intravesical silver nitrate was ineffective for bleeding control, suggesting a limited role for this agent in the management of patients with hemorrhagic cystitis. PMID:27635296

  7. Movie Director Bags a Silver Bear

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Chinese director and film writer Wang Xiaoshuai has walked away with the Silver Bear award at the 58th Berlin International Film Festival for best script of Zuo You, or In Love We Trust. Back in 2001, Wang won his first Silver Bear award for directing Beijing

  8. Topical silver for preventing wound infection

    NARCIS (Netherlands)

    M.N. Storm-Versloot; C.G. Vos; D.T. Ubbink; H. Vermeulen

    2010-01-01

    BACKGROUND: Silver-containing treatments are popular and used in wound treatments to combat a broad spectrum of pathogens, but evidence of their effectiveness in preventing wound infection or promoting healing is lacking. OBJECTIVES: To establish the effects of silver-containing wound dressings and

  9. Innate cation sensitivity in a semiconducting polymer.

    Science.gov (United States)

    Althagafi, Talal M; Algarni, Saud A; Grell, Martin

    2016-09-01

    Water-gated organic thin film transistors (OTFTs) using the hole transporting semiconducting polymer, poly(2,5-bis(3-hexadecylthiophen-2-yl)thieno[3,2-b]thiophene) (PBTTT), show an innate response of their threshold voltage to the addition of divalent metal cations to the gating water, without deliberately introducing an ion-sensitive component. A similar threshold response is shown for several divalent cations, but is absent for monovalent cations. Response is absent for transistors using the inorganic semiconductor ZnO, or the similar organic semiconductor poly(3-hexylthiophene) (rrP3HT), instead of PBTTT. We assign innate cation sensitivity to residues of the organometallic Pd(0) complex used as catalyst in PBTTT synthesis which bears strong resemblance to typical metal chelating agents. Organometallic Pd(0) residues are absent from ZnO, and also from rrP3HT which is polymerised with a different type of catalyst. However, when Pd(0) complex is deliberately added to rrP3HT casting solutions, resulting OTFTs also display threshold response to a divalent cation. PMID:27343580

  10. Single pass kernel -means clustering method

    Indian Academy of Sciences (India)

    T Hitendra Sarma; P Viswanath; B Eswara Reddy

    2013-06-01

    In unsupervised classification, kernel -means clustering method has been shown to perform better than conventional -means clustering method in identifying non-isotropic clusters in a data set. The space and time requirements of this method are $O(n^2)$, where is the data set size. Because of this quadratic time complexity, the kernel -means method is not applicable to work with large data sets. The paper proposes a simple and faster version of the kernel -means clustering method, called single pass kernel k-means clustering method. The proposed method works as follows. First, a random sample $\\mathcal{S}$ is selected from the data set $\\mathcal{D}$. A partition $\\Pi_{\\mathcal{S}}$ is obtained by applying the conventional kernel -means method on the random sample $\\mathcal{S}$. The novelty of the paper is, for each cluster in $\\Pi_{\\mathcal{S}}$, the exact cluster center in the input space is obtained using the gradient descent approach. Finally, each unsampled pattern is assigned to its closest exact cluster center to get a partition of the entire data set. The proposed method needs to scan the data set only once and it is much faster than the conventional kernel -means method. The time complexity of this method is $O(s^2+t+nk)$ where is the size of the random sample $\\mathcal{S}$, is the number of clusters required, and is the time taken by the gradient descent method (to find exact cluster centers). The space complexity of the method is $O(s^2)$. The proposed method can be easily implemented and is suitable for large data sets, like those in data mining applications. Experimental results show that, with a small loss of quality, the proposed method can significantly reduce the time taken than the conventional kernel -means clustering method. The proposed method is also compared with other recent similar methods.

  11. One-Pot Silver Nanoring Synthesis

    Directory of Open Access Journals (Sweden)

    Drogat Nicolas

    2009-01-01

    Full Text Available Abstract Silver colloidal nanorings have been synthesized by reducing silver ions with NaBH4 in trisodium citrate buffers. pH increase, by addition of NaOH, was used to speed up reduction reaction. The UV–vis absorption spectra of resulting silver nanorings showed two peaks accounting for transverse and longitudinal surface plasmon resonance, at ≈400 nm, and between 600 and 700 nm, respectively. The shapes of these silver nanoparticles (nanorings depended on AgNO3/NaBH4 ratio, pH and reaction temperature. Particles were analysed by transmission electron microscopy, scanning electron microscopy and X-ray diffraction. A reaction pathway is proposed to explain silver nanoring formation.

  12. Fluorescent silver nanoparticles via exploding wire technique

    Indian Academy of Sciences (India)

    Alqudami Abdullah; S Annapoorni

    2005-11-01

    Aqueous solution containing spherical silver nanoparticles of 20–80 nm size have been generated using a newly developed novel electro-exploding wire (EEW) technique where thin silver wires have been exploded in double distilled water. Structural properties of the resulted nanoparticles have been studied by means of X-ray diffractometer (XRD) and transmission electron microscopy (TEM). The absorption spectrum of the aqueous solution of silver nanoparticles showed the appearance of a broad surface plasmon resonance (SPR) peak centered at a wavelength of 390 nm. The theoretically generated SPR peak seems to be in good agreement with the experimental one. Strong green fluorescence emission was observed from the water-suspended silver nanoparticles excited with light of wavelengths 340, 360 and 390 nm. The fluorescence of silver nanoparticles could be due to the excitation of the surface plasmon coherent electronic motion with the small size effect and the surface effect considerations.

  13. Effect of silver nitrate concentration of silver nanowires synthesized using a polyol method and their application as transparent conductive films

    Energy Technology Data Exchange (ETDEWEB)

    Lin, Jian-Yang [Department of Electronic Engineering, National Yunlin University of Science and Technology, Yunlin 640, Taiwan (China); Hsueh, Yu-Lee [Graduate School of Engineering Science and Technology, National Yunlin University of Science and Technology, Yunlin 640, Taiwan (China); Huang, Jung-Jie, E-mail: jjhuang@mail.dyu.edu.tw [Department of Industrial Engineering and Management, DaYeh University, Changhua 51591, Taiwan (China); Wu, Jia-Rung [Department of Computer Science and Information Engineering, Asia University, Taichung 413, Taiwan (China)

    2015-06-01

    Silver nanowires were synthesized using a polyol process by employing ethylene glycol, poly(N-vinylpyrrolidone), and silver nitrate as precursors. The concentration of silver nitrate was varied to study the resulting changes in aspect ratios of silver nanowires. The experimental results indicated that the growth characteristics of silver nanowires were affected by the synthesis temperature, the concentration of silver nitrate, and the rate at which silver nitrate was added. Field-emission scanning electron microscopy, UV–visible spectrophotometry, and X-ray diffractometry were employed to characterize the silver nanowires. As the concentration of silver nitrate was reduced, the diameters of the silver nanowires decreased, increasing the aspect ratio. The optimal diameter and length of the silver nanowires were 100 nm and 20 μm, respectively. A thin film composed of silver nanowires exhibited average transmittance of 92.15% at visible wavelengths and a sheet resistance of 20 Ω/sq; such a film could be used as a transparent conductive film in commercial applications. - Highlights: • Using a polyol method to synthesize of silver nanowire • Concentration effect of silver nitrate on the synthesis was discussed. • Seed precursors are not used during the silver nanowire synthesizing. • The silver nanowire diameter and length were 100 nm and 20 μm, respectively. • High transmittance and low sheet resistance of silver nanowire film can be obtained.

  14. Effect of silver nitrate concentration of silver nanowires synthesized using a polyol method and their application as transparent conductive films

    International Nuclear Information System (INIS)

    Silver nanowires were synthesized using a polyol process by employing ethylene glycol, poly(N-vinylpyrrolidone), and silver nitrate as precursors. The concentration of silver nitrate was varied to study the resulting changes in aspect ratios of silver nanowires. The experimental results indicated that the growth characteristics of silver nanowires were affected by the synthesis temperature, the concentration of silver nitrate, and the rate at which silver nitrate was added. Field-emission scanning electron microscopy, UV–visible spectrophotometry, and X-ray diffractometry were employed to characterize the silver nanowires. As the concentration of silver nitrate was reduced, the diameters of the silver nanowires decreased, increasing the aspect ratio. The optimal diameter and length of the silver nanowires were 100 nm and 20 μm, respectively. A thin film composed of silver nanowires exhibited average transmittance of 92.15% at visible wavelengths and a sheet resistance of 20 Ω/sq; such a film could be used as a transparent conductive film in commercial applications. - Highlights: • Using a polyol method to synthesize of silver nanowire • Concentration effect of silver nitrate on the synthesis was discussed. • Seed precursors are not used during the silver nanowire synthesizing. • The silver nanowire diameter and length were 100 nm and 20 μm, respectively. • High transmittance and low sheet resistance of silver nanowire film can be obtained

  15. Corrosion processes of triangular silver nanoparticles compared to bulk silver

    Energy Technology Data Exchange (ETDEWEB)

    Keast, V. J., E-mail: vicki.keast@newcastle.edu.au; Myles, T. A. [University of Newcastle, School of Mathematical and Physical Sciences (Australia); Shahcheraghi, N.; Cortie, M. B. [University of Technology Sydney, Institute for Nanoscale Technology (Australia)

    2016-02-15

    Excessive corrosion of silver nanoparticles is a significant impediment to their use in a variety of potential applications in the biosensing, plasmonic and antimicrobial fields. Here we examine the environmental degradation of triangular silver nanoparticles (AgNP) in laboratory air. In the early stages of corrosion, transmission electron microscopy shows that dissolution of the single-crystal, triangular, AgNP (side lengths 50–120 nm) is observed with the accompanying formation of smaller, polycrystalline Ag particles nearby. The new particles are then observed to corrode to Ag{sub 2}S and after 21 days nearly full corrosion has occurred, but some with minor Ag inclusions remaining. In contrast, a bulk Ag sheet, studied in cross section, showed an adherent corrosion layer of only around 20–50 nm in thickness after over a decade of being exposed to ambient air. The results have implications for antibacterial properties and ecotoxicology of AgNP during corrosion as the dissolution and reformation of Ag particles during corrosion will likely be accompanied by the release of Ag{sup +} ions.

  16. Plasma Catalytic Synthesis of Silver Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    ZHANG Yu-Tao; GUO Ying; MA Teng-Cai

    2011-01-01

    We present the experimental results of plasma catalytic synthesis of colloidal silver nanoparticles, using AgNO3 as the precursor, ethanol as the solvent and reducing agent, and poly vinyl pyrrolidone (PVP) as the macromolecular surfactant. The plasma is generated by an atmospheric argon dielectric barrier discharge jet. Silver nanoparticles are produced instantly once the plasma is ignited. The system is not heated so it is necessary to use traditional chemical methods. The samples are characterized by UV-visible absorbance and transmission electron microscopy. For glow discharge mode no obvious silver nanoparticles are observed. For low voltage filamentary streamer discharge mode a lot of silver nanoparticles with the mean diameter of ~3.5nm are generated and a further increase of the voltage causes the occurrence of agglomeration.%We present the experimental results of plasma catalytic synthesis of colloidal silver nanoparticles,using AgNO3 as the precursor,ethanol as the solvent and reducing agent,and poly vinyl pyrrolidone (PVP) as the macromolecular surfactant.The plasma is generated by an atmospheric argon dielectric barrier discharge jet.Silver nanoparticles are produced instantly once the plasma is ignited.The system is not heated so it is necessary to use traditional chemical methods.The samples are characterized by UV-visible absorbance and transmission electron microscopy.For glow discharge mode no obvious silver nanoparticles are observed.For low voltage filamentary streamer discharge mode a lot of silver nanoparticles with the mean diameter of ~3.5nm are generated and a further increase of the voltage causes the occurrence of agglomeration.The study of silver nanoparticles has been an extremely active area in recent years because of their important physical and chemical properties as a catalyst and antimicrobial reagent,for example.A number of methods for silver nanoparticle preparation have been developed,[1-3] among them chemical reduction is

  17. Forging Colloidal Nanostructures via Cation Exchange Reactions

    Science.gov (United States)

    2016-01-01

    Among the various postsynthesis treatments of colloidal nanocrystals that have been developed to date, transformations by cation exchange have recently emerged as an extremely versatile tool that has given access to a wide variety of materials and nanostructures. One notable example in this direction is represented by partial cation exchange, by which preformed nanocrystals can be either transformed to alloy nanocrystals or to various types of nanoheterostructures possessing core/shell, segmented, or striped architectures. In this review, we provide an up to date overview of the complex colloidal nanostructures that could be prepared so far by cation exchange. At the same time, the review gives an account of the fundamental thermodynamic and kinetic parameters governing these types of reactions, as they are currently understood, and outlines the main open issues and possible future developments in the field. PMID:26891471

  18. Synthesis and Characterization of Sol-Gel Prepared Silver Nanoparticles

    Science.gov (United States)

    Ahlawat, Dharamvir Singh; Kumari, Rekha; Rachna; Yadav, Indu

    2014-03-01

    Silver nanoparticles (SNPs) have been successfully prepared using sol-gel method by annealing the sample at 550°C for 30 min. The SNPs were not confirmed by X-ray diffraction (XRD) analysis when the annealing temperature was considered at 450°C. They were also not confirmed without calcination of the sample. The physical mechanism of silver clusters formation in the densified silica matrix with respect to thermal treatment has been understood. The presence of silver metal in the silica matrix was confirmed by XRD analysis and TEM image of the samples. The average size of nanoparticles dispersed in silica matrix was determined as 10.2 nm by the XRD technique. The synthesized nanocomposites were also characterized by UV-Visible spectroscopy with a peak in the absorption spectra at around 375 nm. The distribution of particle size has been reported here in the range from 8 nm to 25 nm by TEM observations of the sample prepared at 550°C. The spherically smaller size (≈10 nm) SNPs have reported the surface plasmons resonance (SPR) peak less than or near to 400 nm due to blue-shifting and effect of local refractive index. Without annealing the silica samples the absorption spectra does not show any peak around 375 nm. The FTIR spectroscopy of the three types of samples prepared at different temperatures (room temperature, 450°C and 550°C) has also been reported. This spectra have provided the identification of different chemical groups in the prepared samples. It has been predicted that the size of SNPs by XRD, UV-Visible and TEM results have agreed well with each other. It may be concluded that formation of SNPs is a function of annealing temperature.

  19. Suitsetamisega võitlemisel ei aita inimeste kiusamine / Silver Meikar

    Index Scriptorium Estoniae

    Meikar, Silver, 1978-

    2004-01-01

    Suitsetamise vastu võitlemisel ei tohiks kasutada rangelt seadusi vaid võimaldada soodsalt osta suitsetamisvastaseid vahendeid, leiab autor. Vt. ka: Silver Meikar: Olen valmis hoidma Eesti edu; Silver Meikar saatis lugejakirja Saksamaa päevalehtedele; Arvamusi Silver Meikarist; Silver Meikar loobus paberkandjale trükitud seaduseelnõudest

  20. Timescale of silver nanoparticle transformation in neural cell cultures impacts measured cell response

    Energy Technology Data Exchange (ETDEWEB)

    Hume, Stephanie L.; Chiaramonti, Ann N.; Rice, Katherine P.; Schwindt, Rani K. [National Institute of Standards and Technology (NIST), Applied Chemicals and Materials Division (United States); MacCuspie, Robert I. [National Institute of Standards and Technology (NIST), Materials Measurement Science Division (United States); Jeerage, Kavita M., E-mail: jeerage@boulder.nist.gov [National Institute of Standards and Technology (NIST), Applied Chemicals and Materials Division (United States)

    2015-07-15

    Both serum protein concentration and ionic strength are important factors in nanoparticle transformation within cell culture environments. However, silver nanoparticles are not routinely tracked at their working concentration in the specific medium used for in vitro toxicology studies. Here we evaluated the transformation of electrostatically stabilized citrate nanoparticles (C-AgNPs) and sterically stabilized polyvinylpyrrolidone nanoparticles (PVP-AgNPs) in a low-serum (∼ 0.2 mg/mL bovine serum albumin) culture medium, while measuring the response of rat cortex neural progenitor cells, which differentiate in this culture environment. After 24 h, silver nanoparticles at concentrations up to 10 µg/mL did not affect adenosine triphosphate levels, whereas silver ions decreased adenosine triphosphate levels at concentrations of 1.1 µg/mL or higher. After 240 h, both silver nanoparticles, as well as silver ion, unambiguously decreased adenosine triphosphate levels at concentrations of 1 and 1.1 µg/mL, respectively, suggesting particle dissolution. Particle transformation was investigated in 1:10 diluted, 1:2 diluted, or undiluted differentiation medium, all having an identical protein concentration, to separate the effect of serum protein stabilization from ionic strength destabilization. Transmission electron microscopy images indicated that particles in 1:10 medium were not surrounded by proteins, whereas particles became clustered within a non-crystalline protein matrix after 24 h in 1:2 medium and at 0 h in undiluted medium. Despite evidence for a protein corona, particles were rapidly destabilized by high ionic strength media. Polyvinylpyrrolidone increased the stability of singly dispersed particles compared to citrate ligands; however, differences were negligible after 4 h in 1:2 medium or after 1 h in undiluted medium. Thus low-serum culture environments do not provide sufficient colloidal stability for long-term toxicology studies with citrate

  1. Antimicrobial and cytotoxicity effect of silver nanoparticle synthesized by Croton bonplandianum Baill. leaves

    Directory of Open Access Journals (Sweden)

    K. Khanra

    2016-01-01

    Full Text Available Objective(s: For the development of reliable, ecofriendly, less expensive process for the synthesis of silver nanoparticles and to evaluate the bactericidal, and cytotoxicity properties of silver nanoparticles synthesized from root extract of Croton bonplandianum, Baill. Materials and Methods: The synthesis of silver nanoparticles by plant part of Croton bonplandianum was carried out.  The formation of nanoparticles was confirmed by Transmission Electron Microscopy (TEM, Scanning Electron Microscopy (SEM, XRD and UV-Vis spectrophotometric analysis.  The biochemical properties were assayed by antibacterial study, cytotoxicity assay using cancer cell line.  Results: The formation of silver nanoparticles was confirmed by UV-VIS spectroscopic analysis which showed absorbance peak at 425 nm.  X-ray diffraction photograph indicated the face centered cubic structure of the synthesized AgNPs.  TEM has displayed the different dimensional images of biogenic silver nanoparticles with particle size distribution ranging from 15-40 nm with an average size of 32 nm. Silver particles are spherical in shape, clustered.  The EDX analysis was used to identify the elemental composition of synthesized AgNPs. Antibacterial activity of the synthesized AgNPs against three Gram positive and Gram negative bacteria strains like Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa carried out showed significant zones of inhibition. The cytotoxicity study by AgNPS also showed cytotoxicity on ovarian cancer cell line PA-1 and lung epithelial cancer cell line A549.  Conclusion: The present study confirms that the AgNPs have great promise as antibacterial, and anticancer agent.

  2. Timescale of silver nanoparticle transformation in neural cell cultures impacts measured cell response

    International Nuclear Information System (INIS)

    Both serum protein concentration and ionic strength are important factors in nanoparticle transformation within cell culture environments. However, silver nanoparticles are not routinely tracked at their working concentration in the specific medium used for in vitro toxicology studies. Here we evaluated the transformation of electrostatically stabilized citrate nanoparticles (C-AgNPs) and sterically stabilized polyvinylpyrrolidone nanoparticles (PVP-AgNPs) in a low-serum (∼ 0.2 mg/mL bovine serum albumin) culture medium, while measuring the response of rat cortex neural progenitor cells, which differentiate in this culture environment. After 24 h, silver nanoparticles at concentrations up to 10 µg/mL did not affect adenosine triphosphate levels, whereas silver ions decreased adenosine triphosphate levels at concentrations of 1.1 µg/mL or higher. After 240 h, both silver nanoparticles, as well as silver ion, unambiguously decreased adenosine triphosphate levels at concentrations of 1 and 1.1 µg/mL, respectively, suggesting particle dissolution. Particle transformation was investigated in 1:10 diluted, 1:2 diluted, or undiluted differentiation medium, all having an identical protein concentration, to separate the effect of serum protein stabilization from ionic strength destabilization. Transmission electron microscopy images indicated that particles in 1:10 medium were not surrounded by proteins, whereas particles became clustered within a non-crystalline protein matrix after 24 h in 1:2 medium and at 0 h in undiluted medium. Despite evidence for a protein corona, particles were rapidly destabilized by high ionic strength media. Polyvinylpyrrolidone increased the stability of singly dispersed particles compared to citrate ligands; however, differences were negligible after 4 h in 1:2 medium or after 1 h in undiluted medium. Thus low-serum culture environments do not provide sufficient colloidal stability for long-term toxicology studies with citrate

  3. Electrospun polyacrylonitrile nanofibers loaded with silver nanoparticles by silver mirror reaction

    Energy Technology Data Exchange (ETDEWEB)

    Shi, Yongzheng; Li, Yajing; Zhang, Jianfeng; Yu, Zhongzhen; Yang, Dongzhi, E-mail: yangdz@mail.buct.edu.cn

    2015-06-01

    The silver mirror reaction (SMR) method was selected in this paper to modify electrospun polyacrylonitrile (PAN) nanofibers, and these nanofibers loaded with silver nanoparticles showed excellent antibacterial properties. PAN nanofibers were first pretreated in AgNO{sub 3} aqueous solution before the SMR process so that the silver nanoparticles were distributed evenly on the outer surface of the nanofibers. The final PAN nanofibers were characterized by scanning electron microscopy (SEM), energy dispersive spectrometer (EDS), transmission electron microscopy (TEM), TEM-selected area electron diffraction (SAED), X-ray diffraction (XRD) and thermogravimetric analysis (TGA). SEM, TEM micrographs and SAED patterns confirmed homogeneous dispersion of the silver nanoparticles which were composed of monocrystals with diameters 20–30 nm. EDS and XRD results showed that these monocrystals tended to form face-centered cubic single silver. TGA test indicated that the nanoparticles loaded on the nanofibers reached above 50 wt.%. This material was also evaluated by the viable cell-counting method. The results indicated that PAN nanofibers loaded with silver nanoparticles exhibited excellent antimicrobial activities against gram-negative Escherichia coli (E. coli), gram-positive Staphylococcus aureus (S. aureus) and the fungus Monilia albicans. Thus, this material had many potential applications in biomedical fields. - Highlights: • Silver mirror reaction was used to prepare nanofibers loaded with silver nanoparticles. • The SAED patterns demonstrated the monocrystallinity of silver nanocrystals. • The XRD results showed nanoparticles tended to be face-centered cubic single silver. • The material showed excellent antimicrobial activities against bacteria and fungi.

  4. Cationically polymerizable monomers derived from renewable sources

    Energy Technology Data Exchange (ETDEWEB)

    Crivello, J.V.

    1992-10-01

    The objectives of this project are to design and synthesize novel monomers which orginate from renewable biological sources and to carry out their rapid, efficient, pollution-free and energy efficient cationic polymerization to useful products under the influence of ultraviolet light or heat. A summary of the results of the past year's research on cationically polymerizable monomers derived from renewable sources is presented. Three major areas of investigation corresponding to the different classes of naturally occurring starting materials were investigated; epoxidized terpenes and natural rubber and vinyl ethers from alcohols and carbohydrates.

  5. Mixed cation effect in sodium aluminosilicate glasses

    DEFF Research Database (Denmark)

    Kjeldsen, Jonas; Smedskjær, Morten Mattrup; Mauro, John C.;

    , network structure, and the resistances associated with the deformation processes in mixed cation glasses by partially substituting magnesium for calcium and calcium for lithium in sodium aluminosilicate glasses. We use Raman and 27Al NMR spectroscopies to obtain insights into the structural...... and topological features of these glasses and we use AFM to quantify the resistances associated with each deformation process under Vickers indentation. We demonstrate that the mixed cation effect manifests itself as a maximum in the amount of bonded tetrahedral units and as a minimum in liquid fragility index...

  6. Cation Effect on Copper Chemical Mechanical Polishing

    Institute of Scientific and Technical Information of China (English)

    WANG Liang-Yong; LIU Bo; SONG Zhi-Tang; FENG Song-Lin

    2009-01-01

    We examine the effect of cations in solutions containing benzotriazole (BTA) and H2O2 on copper chemical mechanical polishing (CMP). On the base of atomic force microscopy (AFM) and material removal rate (MRR) results, it is found that ammonia shows the highest MRR as well as good surface after CMP, while KOH demon-strates the worst performance. These results reveal a mechanism that sma//molecules with lone-pairs rather than molecules with steric effect and common inorganic cations are better for copper CMP process, which is indirectly confirmed by open circuit potential (OCP).

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

    Institute of Scientific and Technical Information of China (English)

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

    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(1.5-3.0μm)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.

  8. Comparative Assessment of Antimicrobial Efficiency of Ionic Silver, Silver Monoxide, and Metallic Silver Incorporated onto an Aluminum Oxide Nanopowder Carrier

    OpenAIRE

    Agnieszka Maria Jastrzębska; Ewa Karwowska; Andrzej R. Olszyna; Antoni R. Kunicki

    2013-01-01

    The present paper provides comparative assessment of antimicrobial efficiency of ionic silver (Ag+), silver monoxide (Ag2O), and metallic silver (Ag) incorporated onto an aluminum oxide nanopowder carrier (Al2O3). The deposition of Ag+ ions, Ag2O nanoparticles, and Ag nanoparticles on an different phases of aluminum oxide nanopowder carrier was realized using consecutive stages of dry sol-gel method. The Al2O3-Ag+, Al2O3-Ag2O, and Al2O3-Ag nanopowders were widely characterized qualitatively a...

  9. Globular Cluster Formation in the Virgo Cluster

    CERN Document Server

    Moran, C Corbett; Lake, G

    2014-01-01

    Metal poor globular clusters (MPGCs) are a unique probe of the early universe, in particular the reionization era. Systems of globular clusters in galaxy clusters are particularly interesting as it is in the progenitors of galaxy clusters that the earliest reionizing sources first formed. Although the exact physical origin of globular clusters is still debated, it is generally admitted that globular clusters form in early, rare dark matter peaks (Moore et al. 2006; Boley et al. 2009). We provide a fully numerical analysis of the Virgo cluster globular cluster system by identifying the present day globular cluster system with exactly such early, rare dark matter peaks. A popular hypothesis is that that the observed truncation of blue metal poor globular cluster formation is due to reionization (Spitler et al. 2012; Boley et al. 2009; Brodie & Strader 2006); adopting this view, constraining the formation epoch of MPGCs provides a complementary constraint on the epoch of reionization. By analyzing both the l...

  10. Cation Selectivity in Biological Cation Channels Using Experimental Structural Information and Statistical Mechanical Simulation.

    Directory of Open Access Journals (Sweden)

    Justin John Finnerty

    Full Text Available Cation selective channels constitute the gate for ion currents through the cell membrane. Here we present an improved statistical mechanical model based on atomistic structural information, cation hydration state and without tuned parameters that reproduces the selectivity of biological Na+ and Ca2+ ion channels. The importance of the inclusion of step-wise cation hydration in these results confirms the essential role partial dehydration plays in the bacterial Na+ channels. The model, proven reliable against experimental data, could be straightforwardly used for designing Na+ and Ca2+ selective nanopores.

  11. Simultaneous anion and cation mobility in polypyrrole

    DEFF Research Database (Denmark)

    Skaarup, Steen; Bay, Lasse; Vidanapathirana, K.;

    2003-01-01

    Polypyrrole (PPy) polymer films permanently doped with large, immobile anion dodecyl benzene sulfonate (DBS) have been characterized by cyclic voltammetry in order to clarify the roles of cations and anions in the aqueous electrolyte as mobile ions in the film. Aqueous solutions of 0.05-0.1 M alk...

  12. Resonance raman studies of phenylcyclopropane radical cations

    NARCIS (Netherlands)

    Godbout, J.T.; Zuilhof, H.; Heim, G.; Gould, I.R.; Goodman, J.L.; Dinnocenzo, J.P.; Myers Kelley, A.

    2000-01-01

    Resonance Raman spectra of the radical cations of phenylcyclopropane and trans-1-phenyl-2-methylcyclopropane are reported. A near-UV pump pulse excites a photosensitizer which oxidizes the species of interest, and a visible probe pulse delayed by 35 ns obtains the spectrum of the radical ion. The tr

  13. Anionic/cationic complexes in hair care.

    Science.gov (United States)

    O'Lenick, Tony

    2011-01-01

    The formulation of cosmetic products is always more complicated than studying the individual components in aqueous solution. This is because there are numerous interactions between the components, which make the formulation truly more than the sum of the parts. This article will look at interactions between anionic and cationic surfactants and offer insights into how to use these interactions advantageously in making formulations.

  14. Room-temperature silver-containing liquid metal salts with nitrate anions.

    Science.gov (United States)

    Schaltin, Stijn; Brooks, Neil R; Sniekers, Jeroen; Depuydt, Daphne; Van Meervelt, Luc; Binnemans, Koen; Fransaer, Jan

    2013-11-21

    The synthesis, structural, thermal and electrochemical properties of fluorine-free silver-containing ionic liquids are presented. The ionic liquid cations are formed by a silver(i) ion surrounded by two 1-alkylimidazole ligands, with the counter anions being nitrate ions. Depending on the alkyl chain length, the complexes were found to be liquids at room temperature or melting slightly above this. For the solid compounds it was possible to elucidate the structure by single crystal X-ray analysis. The ionic liquids are electroactive, have good mass transport properties and can be used for the electrodeposition of silver at high current densities. The thermal properties and stability of these compounds were tested by differential scanning calorimetry and thermogravimetric analysis. The viscosity of the ionic liquids follows a Vogel-Tamman-Fulcher relationship as a function of temperature. The electrochemical properties of the complexes were tested by cyclic voltammetry and the resulting electrodeposits were examined using scanning electron microscopy and atomic force microscopy. PMID:24097139

  15. Laser Treatment of Cotton Fabric for Durable Antibacterial Properties of Silver Nanoparticles

    Directory of Open Access Journals (Sweden)

    Shirin Nourbakhsh

    2012-07-01

    Full Text Available In the present study, cotton fabric was exposed to laser exposure at different energy levels and then the silver nanoparticles were coated on untreated and laser treated cotton fabrics. Methylene blue dye was used to detect the presence of carboxylic acid groups (-COO on laser treated cotton and the dye absorption results were determined spectrophotometrically. ICP-OES (Inductively Coupled Plasma Optical Emission Spectroscopy analysis and antibacterial tests were carried out to investigate the silver ion content and bactericidal properties of silver nanoparticles on cotton fabrics. Infrared spectroscopy (FTIR/ATR analysis and scanning electron microscopy (SEM were used to identify chemical changes and to study the morphology of the surface of the fibers. EDAX (Energy Dispersive X-ray Spectroscopy analysis was calculated for SEM micrographs. The results showed according to the higher uptake of methylene blue dye that the negative charge of the carboxylic acid groups had been created by laser treatment. Although the FTIR spectroscopy results did not show an increase in carboxylic acid groups, the cationic dye absorption increased. The durability of the Ag+ ion particles on repeated laundered laser treated cotton was proven by antibacterial and ICP tests, particularly when the laser energy was increased.

  16. Interaction of (-)-epigallocatechin gallate with silver nanoparticles

    CERN Document Server

    Chandra, Goutam Kumar; Dasgupta, Swagata; Roy, Anushree

    2010-01-01

    Interactions between silver nanoparticles and (-)-epigallocatechin gallate (EGCG) have been investigated. Prior to the addition of EGCG molecules the silver particles are stabilized by borate ions. Studies on the surface plasmon resonance band of silver particles suggest that the EGCG molecules remove the borate ions from the surface of the metal particles due to the chelating property of the ions. The complex formation by EGCG and borate ions has been confirmed by NMR studies and pH titration. A possible scheme of interaction between the two has been proposed.

  17. Anti-bacterial Studies of Silver Nanoparticles

    CERN Document Server

    Theivasanthi, T

    2011-01-01

    We discuss about the antibacterial activities of Silver nanoparticles and compare them on both Gram negative and Gram positive bacteria in this investigation. The activities of Silver nanoparticles synthesized by electrolysis method are more in Gram (-) than Gram (+) bacteria. First time, we increase its antibacterial activities by using electrical power while on electrolysis synthesis and it is confirmed from its more antibacterial activities (For Escherichia coli bacteria). We investigate the changes of inner unit cell Lattice constant of Silver nanoparticles prepared in two different methods and its effects on antibacterial activities. We note that slight change of the lattice constant results in the enhancement of its antibacterial activities.

  18. Preparation of silver powder through glycerol process

    Indian Academy of Sciences (India)

    Amit Sinha; B P Sharma

    2005-06-01

    High purity fine silver powder with uniform particle morphology was prepared through glycerol process. The process involves reduction of silver nitrate by glycerol under atmospheric conditions at a temperature below 175°C. Glycerol, in this process, acts as a solvent as well as a reducing agent. The powders prepared through this process were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and chemical analysis. The powders were well crystalline and contained oxygen, carbon and hydrogen as impurities. Overall purity was better than 99.9%. The yield of silver powder was better than 99%.

  19. Synthesis and characterization of nanophased silver tungstate

    Indian Academy of Sciences (India)

    Thresiamma George; Sunny Joseph; Suresh Mathew

    2005-11-01

    Silver tungstate (Ag2WO4) nanoparticles in two different morphologies are prepared by controlling the reaction kinetics of aqueous precipitation. X-ray diffraction studies reveal that the silver tungstate nanoparticles are in the -phase. SEM images show the rod-like and fiber-like morphologies of the nanoparticles with high aspect ratios. The TGA and DTA studies show the high thermal stability of the nanorods. The average crystallite sizes (20–30 nm) of the rod-like silver tungstate estimated from TEM is consistent with the XRD results.

  20. Preparation of Silver Nanostructures from Bicontinuous Microemulsions

    OpenAIRE

    Pedroza-Toscano, M. A.; Rabelero-Velasco, M.; Díaz de León, R.; H. Saade; R. G. López; E. Mendizábal; Puig, J. E.

    2012-01-01

    Precipitation of silver nanoparticles at 70°C was carried out by dosing a 1.3 M sodium borohydride aqueous solution over bicontinuous microemulsions formed with a mixture of sodium bis(2-ethylhexyl) sulfosuccinate (AOT) and sodium dodecylsulfate (SDS) as surfactants, a 0.5 M silver nitrate aqueous solution, and toluene. Weight ratios of 2.5/1 and 3/1 AOT/SDS were used in the precipitation reactions. Silver nanoparticles were characterized by transmission electronic microscopy, X-ray diffracti...

  1. Synthesis of silver nanoparticles and antibacterial property of silk fabrics treated by silver nanoparticles

    OpenAIRE

    ZHANG, GUANGYU; Liu, Yan; Gao, Xiaoliang; Chen, Yuyue

    2014-01-01

    A silver nanoparticle solution was prepared in one step by mixing AgNO3 and a multi-amino compound (RSD-NH2) solution under ambient condition. RSD-NH2 was in-house synthesized by methacrylate and polyethylene polyamine in methanol, which has abundant amino and imino groups. However, the characterization of silver nanoparticles indicated that these nanoparticles are easy to agglomerate in solution. Therefore, an in situ synthesis method of silver nanoparticles on the silk fabrics was developed...

  2. Cationic lipids and cationic ligands induce DNA helix denaturation: detection of single stranded regions by KMnO4 probing.

    Science.gov (United States)

    Prasad, T K; Gopal, Vijaya; Rao, N Madhusudhana

    2003-09-25

    Cationic lipids and cationic polymers are widely used in gene delivery. Using 1,2-dioleoyl-3-trimethylammonium-propane (DOTAP) as a cationic lipid, we have investigated the stability of the DNA in DOTAP:DNA complexes by probing with potassium permanganate (KMnO4). Interestingly, thymidines followed by a purine showed higher susceptibility to cationic ligand-mediated melting. Similar studies performed with other water-soluble cationic ligands such as polylysine, protamine sulfate and polyethyleneimine also demonstrated melting of the DNA but with variations. Small cations such as spermine and spermidine and a cationic detergent, cetyl trimethylammonium bromide, also rendered the DNA susceptible to modification by KMnO4. The data presented here provide direct proof for melting of DNA upon interaction with cationic lipids. Structural changes subsequent to binding of cationic lipids/ligands to DNA may lead to instability and formation of DNA bubbles in double-stranded DNA.

  3. Formation of silver nanoparticles inside a soda-lime glass matrix in the presence of a high intensity Ar+ laser beam

    International Nuclear Information System (INIS)

    Formation and motion of the silver nanoparticles inside an ion-exchanged soda-lime glass in the presence of a focused high intensity continuous wave Ar+ laser beam (intensity: 9.2 x 104 W/cm2) have been studied in here. One-dimensional diffusion equation has been used to model the diffusion of the silver ions into the glass matrix, and a two-dimensional reverse diffusion model has been introduced to explain the motion of the silver clusters and their migration toward the glass surface in the presence of the laser beam. The results of the mentioned models were in agreement with our measurements on thickness of the ion-exchange layer by means of optical microscopy and recorded morphology of the glass surface around the laser beam axis by using a Mirau interferometer. SEM micrographs were used to extract the size distribution of the migrated silver particles over the glass surface.

  4. Solid state and aqueous behavior of uranyl peroxide cage clusters

    Science.gov (United States)

    Pellegrini, Kristi Lynn

    Uranyl peroxide cage clusters include a large family of more than 50 published clusters of a variety of sizes, which can incorporate various ligands including pyrophosphate and oxalate. Previous studies have reported that uranyl clusters can be used as a method to separate uranium from a solid matrix, with potential applications in reprocessing of irradiated nuclear fuel. Because of the potential applications of these novel structures in an advanced nuclear fuel cycle and their likely presence in areas of contamination, it is important to understand their behavior in both solid state and aqueous systems, including complex environments where other ions are present. In this thesis, I examine the aqueous behavior of U24Pp 12, as well as aqueous cluster systems with added mono-, di-, and trivalent cations. The resulting solutions were analyzed using dynamic light scattering and ultra-small angle X-ray scattering to evaluate the species in solution. Precipitates of these systems were analyzed using powder X-ray diffraction, X-ray fluorescence spectrometry, and Raman spectroscopy. The results of these analyses demonstrate the importance of cation size, charge, and concentration of added cations on the aqueous behavior of uranium macroions. Specifically, aggregates of various sizes and shapes form rapidly upon addition of cations, and in some cases these aggregates appear to precipitate into an X-ray amorphous material that still contains U24Pp12 clusters. In addition, I probe aggregation of U24Pp12 and U60, another uranyl peroxide cage cluster, in mixed solvent water-alcohol systems. The aggregation of uranyl clusters in water-alcohol systems is a result of hydrogen bonding with polar organic molecules and the reduction of the dielectric constant of the system. Studies of aggregation of uranyl clusters also allow for comparison between the newer uranyl polyoxometalate family and century-old transition metal polyoxometalates. To complement the solution studies of uranyl

  5. Ultrastructural localization of silver in rat testis and organ distribution of radioactive silver in the rat

    DEFF Research Database (Denmark)

    Ernst, E; Rungby, J; Baatrup, E

    1992-01-01

    , concentrations in organs remained almost stable throughout the experimental period. Silver was especially abundant in interstitial macrophages and in the basement membrane. Deposits of silver were found in all cell types of spermatogenesis and in the lysosomes of the Sertoli cells. Udgivelsesdato: 1991-Oct......The deposition of silver after a single intravenous injection (2 micrograms Ag g-1 body weight) was studied in the testes of Wistar rats 24 h and 1 and 2 weeks after dosing with radiolabelled 110AgNo3 (2 micrograms Ag and 1.2 kBq g-1 body weight). Also, the temporal accumulation of silver during...

  6. Preparations and characterization of alginate/silver composite films: Effect of types of silver particles.

    Science.gov (United States)

    Shankar, Shiv; Wang, Long-Feng; Rhim, Jong-Whan

    2016-08-01

    Alginate-based films reinforced with different types of silver particles such as metallic silver (AgM), silver zeolite (AgZ), citrate reduced silver nanoparticles (AgNP(C)), laser ablated silver nanoparticles (AgNP(LA)), and silver nitrate (AgNO3) were prepared using a solvent casting method and the effect of silver particles on the optical, mechanical, water vapor barrier, and antimicrobial properties the composite films was evaluated. Size and shape of the silver particles were varied depending on the types of silver source and the preparation method. The alginate films incorporated with AgNP(C), AgNP(LA), and AgNO3 showed a characteristic surface plasmon resonance absorption peaks of AgNPs around 420nm. Film properties such as mechanical, optical, and water vapor barrier properties were greatly influenced by the types of AgNPs used. Alginate/AgNPs composite films except AgM and AgNP(LA) incorporated ones exhibited strong antimicrobial activity against two food-borne pathogenic bacteria, Escherichia coli and Listeria monocytogenes. The developed films have a high potential for the application as antimicrobial food packaging films. PMID:27112867

  7. Two Possible Configurations for Silver-C60-Silver Molecular Devices and Their Conductance Characteristics

    Institute of Scientific and Technical Information of China (English)

    TIAN Guang-Jun; SU Wen-Yong

    2009-01-01

    Coherent electronic transport properties of silver-C60-silver molecular junctions in different configurations are studied using hybrid density function theory.The experimentally measured current flows of C60 molecules adsorbed on the diver surface are well reproduced by theoretical calculations.It is found that the current-voltage characteristics of the molecular junctions depend strongly on the configurations of the junctions.Transmission spectra combined with density of states can help us to understand in depth the transport properties.Different kinds of electrode construction are also discussed.With the help of the calculation,two possible configurations of silver-C60-silver molecular junctions are suggested.

  8. Preparation of glasses and glass ceramics of heavy metal oxides containing silver: optical, structural and electrochemical properties

    Directory of Open Access Journals (Sweden)

    Bruna A. Bregadiolli

    2012-01-01

    Full Text Available Silver containing heavy metal oxide glasses and glass ceramics of the system WO3-SbPO4-PbO-AgCl with different AgCl contents have been prepared and their thermal, structural and optical properties characterized. Glass ceramics containing metallic silver nanoparticles have been prepared by annealing glass samples at temperatures above the glass transition and analyzed by transmission electron microscopy and energy dispersive X-ray microanalysis. The presence of the metallic clusters has been also confirmed by the observation of a surface plasmon resonance band in the visible range. Cyclic voltammetric measurements indicated the presence of metallic silver into the glasses, even before to perform the thermal treatment.

  9. Preparation and characterization of nanosized silver phosphate loaded hydroxyapatite by single step co-conversion process

    International Nuclear Information System (INIS)

    The preparation and characterization of silver phosphate nanoparticles loaded hydroxyapatite aiming to enhance the bactericidal performance by a single step co-conversion technique using low temperature phosphorization in the presence of various silver nitrate concentration (AgNO3, ranging 0.001–0.1 M) was performed. Characterization by using X-ray diffraction, infrared spectroscopy and transmission electron microscopy showed that hydroxyapatite and silver phosphate were the main phases in all converted samples and the microstructure comprised the distribution of spherical-shaped silver phosphate nanoparticles within the cluster of hydroxyapatite nanocrystals. Total silver content (ranging 0.09–5.6%) in the converted samples was found to increase with increasing silver nitrate content. Flexural modulus and strength of converted samples remained unchanged for samples using silver nitrate between 0.001 and 0.01 M, but decreased at greater silver nitrate concentration. Antibacterial activity of two selected samples (0.001 and 0.005 M AgNO3) against two bacterial strains (Pseudomonas aeruginosa and Staphylococcus aureus) was observed since 100% reduction of viable cells after 24 h contact was detected. Cytotoxic potential by MTT assay of sample using 0.001 M AgNO3 was only observed at 24 h extraction, but was seen at all extraction periods (24–72 h) for sample using 0.005 M AgNO3. Highlights: ► Low temperature and single step process for producing nanosized Ag3PO4/HA. ► Ag3PO4 content (0.09–5.6%) increased with increasing AgNO3 (0.001–0.1 M). ► Mean particle size of formed Ag3PO4 was less than 5 nm. ► Flexural properties of Ag3PO4/HA was comparable to HA when using AgNO3 3PO4/HA showed antibacterial activity against gram positive and negative strains.

  10. Mechanisms of Silver Nanoparticle Toxicity

    DEFF Research Database (Denmark)

    Foldbjerg, Rasmus

    The rapidly growing field of nanotechnology holds great promise for scientific advancement in many sectors such as medicine, consumer products, energy, and materials. In general terms, nanotechnology covers engineered structures, devices, and systems that have a length scale between 1 and 100...... nanometers. At this size, materials begin to exhibit unique properties that affect physical, chemical, and biological behavior. However, the same characteristics which make nanomaterials attractive for exploitation in new products have led to concerns that nanomaterials may pose a risk for humans...... related to the response caused by Ag NPs, our findings suggested that Ag NPs, due to their particulate form, affect exposed cells in a more complex way than silver ions....

  11. Shaped gold and silver nanoparticles

    Science.gov (United States)

    Sun, Yugang; An, Changhua

    2011-03-01

    Advance in the synthesis of shaped nanoparticles made of gold and silver is reviewed in this article. This review starts with a new angle by analyzing the relationship between the geometrical symmetry of a nanoparticle shape and its internal crystalline structures. According to the relationship, the nanoparticles with well-defined shapes are classified into three categories: nanoparticles with single crystallinity, nanoparticles with angular twins, and nanoparticles with parallel twins. Discussion and analysis on the classical methods for the synthesis of shaped nanoparticles in each category are also included and personal perspectives on the future research directions in the synthesis of shaped metal nanoparticles are briefly summarized. This review is expected to provide a guideline in designing the strategy for the synthesis of shaped nanoparticles and analyzing the corresponding growth mechanism.

  12. Cation-cation interactions, magnetic communication and reactivity of the pentavalent uraniumion [U(NR)2]+

    Energy Technology Data Exchange (ETDEWEB)

    Spencer, Liam P [Los Alamos National Laboratory; Schelter, Eric J [Los Alamos National Laboratory; Boncella, James M [Los Alamos National Laboratory; Yang, Ping [Los Alamos National Laboratory; Gsula, Robyn L [NON LANL; Scott, Brian L [Los Alamos National Laboratory; Thompson, Joe D [Los Alamos National Laboratory; Kiplinger, Jacqueline L [Los Alamos National Laboratory; Batista, Enrique R [Los Alamos National Laboratory

    2009-01-01

    The dimeric bis(imido) uranium complex [{l_brace}U(NtBu)2(I)(tBu2bpy){r_brace}2] (see picture; U green, N blue, I red) has cation-cation interactions between [U(NR)2]+ ions. This f1-f1 system also displays f orbital communication between uranium(V) centers at low temperatures, and can be oxidized to generate uranium(VI) bis(imido) complexes.

  13. Land cover classification using reformed fuzzy C-means

    Indian Academy of Sciences (India)

    B Sowmya; B Sheelarani

    2011-04-01

    This paper explains the task of land cover classification using reformed fuzzy C means. Clustering is the assignment of objects into groups called clusters so that objects from the same cluster are more similar to each other than objects from different clusters. The most basic attribute for clustering of an image is its luminance amplitude for a monochrome image and colour components for a colour image. Since there are more than 16 million colours available in any given image and it is difficult to analyse the image on all of its colours, the likely colours are grouped together by clustering techniques. For that purpose reformed fuzzy C means algorithm has been used. The segmented images are compared using image quality metrics. The image quality metrics used are peak signal to noise ratio (PSNR), error image and compression ratio. The time taken for image segmentation is also used as a comparison parameter. The techniques have been applied to classify the land cover.

  14. Ellipsometric Studies on Silver Telluride Thin Films

    Directory of Open Access Journals (Sweden)

    M. Pandiaraman

    2011-01-01

    Full Text Available Silver telluride thin films of thickness between 45 nm and 145 nm were thermally evaporated on well cleaned glass substrates at high vacuum better than 10 – 5 mbar. Silver telluride thin films are polycrystalline with monoclinic structure was confirmed by X-ray diffractogram studies. AFM and SEM images of these films are also recorded. The phase ratio and amplitude ratio of these films were recorded in the wavelength range between 300 nm and 700 nm using spectroscopic ellipsometry and analysed to determine its optical band gap, refractive index, extinction coefficient, and dielectric functions. High absorption coefficient determined from the analysis of recorded spectra indicates the presence of direct band transition. The optical band gap of silver telluride thin films is thickness dependent and proportional to square of reciprocal of thickness. The dependence of optical band gap of silver telluride thin films on film thickness has been explained through quantum size effect.

  15. Sealed Cylindrical Silver/Zinc Batteries Project

    Data.gov (United States)

    National Aeronautics and Space Administration — RBC Technologies has significanly improved the cycle life and wet life of silver/zinc battery technology through novel separator and anode formulations. This...

  16. Tartu on Eesti Boston / Silver Meikar

    Index Scriptorium Estoniae

    Meikar, Silver, 1978-

    2007-01-01

    Tartu eeldustest kujuneda hariduse, innovaatilise tootmise, pärimuskultuuri ja linnaruumi tasakaalustatud kasutamise südameks. Ettevõtluse, transpordi ja turismi arengust. Lisa: Silver Meikari Lõuna-Eesti edu top 10

  17. Green synthesis of silver nanoparticles using tannins

    Science.gov (United States)

    Raja, Pandian Bothi; Rahim, Afidah Abdul; Qureshi, Ahmad Kaleem; Awang, Khalijah

    2014-09-01

    Colloidal silver nanoparticles were prepared by rapid green synthesis using different tannin sources as reducing agent viz. chestnut (CN), mangrove (MG) and quebracho (QB). The aqueous silver ions when exposed to CN, MG and QB tannins were reduced which resulted in formation of silver nanoparticles. The resultant silver nanoparticles were characterized using UV-Visible, X-ray diffraction (XRD), scanning electron microscopy (SEM/EDX), and transmission electron microscopy (TEM) techniques. Furthermore, the possible mechanism of nanoparticles synthesis was also derived using FT-IR analysis. Spectroscopy analysis revealed that the synthesized nanoparticles were within 30 to 75 nm in size, while XRD results showed that nanoparticles formed were crystalline with face centered cubic geometry.

  18. In situ SU-8 silver nanocomposites

    DEFF Research Database (Denmark)

    Fischer, Søren Vang; Uthuppu, Basil; Jakobsen, Mogens Havsteen

    2015-01-01

    Nanocomposite materials containing metal nanoparticles are of considerable interest in photonics and optoelectronics applications. However, device fabrication of such materials always encounters the challenge of incorporation of preformed nanoparticles into photoresist materials. As a solution...... to this problem, an easy new method of fabricating silver nanocomposites by an in situ reduction of precursors within the epoxy-based photoresist SU-8 has been developed. AgNO3 dissolved in acetonitrile and mixed with the epoxy-based photoresist SU-8 forms silver nanoparticles primarily during the pre- and post...... silver nanocomposite materials can be spin coated as homogeneous thin films and structured by using UV lithography. A resolution of 5 mu m is achieved in the lithographic process. The UV exposure time is found to be independent of the nanoparticle concentration. The fabricated silver nanocomposites...

  19. Realistic Silver Optical Constants for Plasmonics.

    Science.gov (United States)

    Jiang, Yajie; Pillai, Supriya; Green, Martin A

    2016-01-01

    Silver remains the preferred conductor for optical and near-infrared plasmonics. Many high-profile studies focus exclusively on performance simulation in such applications. Almost invariably, these use silver optical data either from Palik's 1985 handbook or, more frequently, an earlier Johnson and Christy (J&C) tabulation. These data are inconsistent, making it difficult to ascertain the reliability of the simulations. The inconsistency stems from challenges in measuring representative properties of pristine silver, due to tarnishing on air exposure. We demonstrate techniques, including use of silicon-nitride membranes, to access the full capabilities of multiple-angle, spectrometric-ellipsometry to generate an improved data set, representative of overlayer-protected, freshly-deposited silver films on silicon-nitride and glass. PMID:27470307

  20. Electrolytic silver ion cell sterilizes water supply

    Science.gov (United States)

    Albright, C. F.; Gillerman, J. B.

    1968-01-01

    Electrolytic water sterilizer controls microbial contamination in manned spacecraft. Individual sterilizer cells are self-contained and require no external power or control. The sterilizer generates silver ions which do not impart an unpleasant taste to water.

  1. Cluster Decline and Resilience

    DEFF Research Database (Denmark)

    Østergaard, Christian Richter; Park, Eun Kyung

    Most studies on regional clusters focus on identifying factors and processes that make clusters grow. However, sometimes technologies and market conditions suddenly shift, and clusters decline. This paper analyses the process of decline of the wireless communication cluster in Denmark, 1963...... in new resources to the cluster but being quick to withdraw in times of crisis....

  2. Electrocatalytic activity of bismuth doped silver electrodes

    CERN Document Server

    Amjad, M

    2002-01-01

    Investigation of redox reactions on silver, and bismuth doped silver electrodes in aqueous KOH solutions, by using potentiostatic steady-state polarization technique, has been carried out. The redox wave potential and current displacements along with multiplicity of the latter have been examined. These electrodes were employed for the oxidation of organic molecules such as ethylamine in alkaline media. Subsequently, these electrodes were ranked with respect to their activity for the redox reactions. (author)

  3. Gold and Silver as Monetary Metals

    OpenAIRE

    John Cooper

    2006-01-01

    Commodity money systems, based upon gold or silver, provided relative economic stability for centuries. On the other hand, our modern paper money system, based upon unbacked government liabilities, is particularly vulnerable to abuse. The various financial crises during the twentieth century bear witness to that. This paper seeks to explain the mechanics of the former Gold and Silver Standards and provides an overview of America’s experience with its bimetallic system.

  4. Gold and Silver Extraction from Leach Solutions

    Directory of Open Access Journals (Sweden)

    Bagdaulet K. Kenzhaliyev

    2014-03-01

    Full Text Available There has been carried out an investigation on the extraction of gold and silver from thiosulfate solutions: standard test and technological solutions of chemical and electrochemical leaching. The influence of related metals on the process of extracting gold from solution was studied. There has been conducted a comparative study of the IR spectra of solutions after the sorption of gold, silver and related metals.

  5. Characterisations of collagen-silver-hydroxyapatite nanocomposites

    Science.gov (United States)

    Ciobanu, C. S.; Popa, C. L.; Petre, C. C.; Jiga, G.; Trusca, R.; Predoi, D.

    2016-05-01

    The XRD analysis were performed to confirm the formation of hydroxyapatite structure in collagen-silver-hydroxyapatite nanocomposites. The molecular interaction in collagen-hydroxyapatite nanocomposites was highlighted by Fourier transform infrared spectroscopy (FTIR) analysis. The SEM showed a nanostructure of collagen-silverhydroxyapatite nanocomposites composed of nano needle-like particles in a veil with collagen texture. The presence of vibrational groups characteristics to the hydroxyapatite structure in collagen-silver-hydroxyapatite (AgHApColl) nanocomposites was investigated by FTIR.

  6. 'Chrysanthemum petal' arrangements of silver nano wires.

    Science.gov (United States)

    Cui, Hui-Wang; Jiu, Jin-Ting; Sugahara, Tohru; Nagao, Shijo; Suganuma, Katsuaki; Uchida, Hiroshi

    2014-12-01

    Highly ordered 'Chrysanthemum petal' arrangements of silver nano wires were fabricated in a biodegradable polymer of polyvinyl alcohol using a simple one-step blending method without any template. The degree of the arrangement increased with the decreasing content of polyvinyl alcohol. The mechanism for the formation of these 'Chrysanthemum petal' arrangements was discussed specifically. These 'Chrysanthemum petal' arrangements will be helpful to increase the electrical conductivity of silver nano wires films. PMID:25397618

  7. Silver nanoparticles - Wolves in sheep's clothing?

    DEFF Research Database (Denmark)

    Foldbjerg, Rasmus Bruno; Jiang, Xiumei; Micləuş, Teodora;

    2015-01-01

    Silver nanoparticles (Ag NPs) are one of the most widely utilized engineered nanomaterials (ENMs) in commercial products due to their effective antibacterial activity, high electrical conductivity, and optical properties. Therefore, they have been one of the most intensively investigated nanomate......Silver nanoparticles (Ag NPs) are one of the most widely utilized engineered nanomaterials (ENMs) in commercial products due to their effective antibacterial activity, high electrical conductivity, and optical properties. Therefore, they have been one of the most intensively investigated...

  8. Selective Electroless Silver Deposition on Graphene Edges

    DEFF Research Database (Denmark)

    Durhuus, D.; Larsen, M. V.; Andryieuski, Andrei;

    2015-01-01

    We demonstrate a method of electroless selective silver deposition on graphene edges or between graphene islands without covering the surface of graphene. Modifications of the deposition recipe allow for decoration of graphene edges with silver nanoparticles or filling holes in damaged graphene...... on silica substrate and thus potentially restoring electric connectivity with minimal influence on the overall graphene electrical and optical properties. The presented technique could find applications in graphene based transparent conductors as well as selective edge functionalization and can be extended...

  9. In vitro percutaneous penetration and characterization of silver from silver-containing textiles.

    Science.gov (United States)

    Bianco, Carlotta; Kezic, Sanja; Crosera, Matteo; Svetličić, Vesna; Šegota, Suzana; Maina, Giovanni; Romano, Canzio; Larese, Francesca; Adami, Gianpiero

    2015-01-01

    The objective of this study was to determine the in vitro percutaneous penetration of silver and characterize the silver species released from textiles in different layers of full thickness human skin. For this purpose, two different wound dressings and a garment soaked in artificial sweat were placed in the donor compartments of Franz cells for 24 hours. The concentration of silver in the donor phase and in the skin was determined by an electrothermal atomic absorption spectrometer (ET-AAS) and by inductively coupled plasma mass spectrometer (ICP-MS). The characterization of silver species in the textiles and in the skin layers was made by scanning electron microscopy with integrated energy dispersive X-ray spectroscopy (SEM-EDX). Additionally, the size distribution of silver nanoparticles in the textiles was performed by atomic force microscopy (AFM). On the surface of all investigated materials, silver nanoparticles of different size and morphology were found. Released silver concentrations in the soaking solutions (ie, exposure concentration) ranged from 0.7 to 4.7 μg/mL (0.6-4.0 μg/cm(2)), fitting the bactericidal range. Silver and silver chloride aggregates at sizes of up to 1 μm were identified both in the epidermis and dermis. The large size of these particles suggests that the aggregation occurred in the skin. The formation of these aggregates likely slowed down the systemic absorption of silver. Conversely, these aggregates may form a reservoir enabling prolonged release of silver ions, which might lead to local effects.

  10. Transition metal cations extraction by ester and ketone derivatives of chromogenic azocalix[4]arenes.

    Science.gov (United States)

    Ak, Metin; Taban, Deniz; Deligöz, Hasalettin

    2008-06-15

    The molecule of azocalix[n]arene is a macrocyclic used effectively in the complexation of the heavy metal pollutants (like silver and mercury). In this work, our main aim is to prepare new chromogenic azocalix[n]arene molecules to elaborate an extractant with high extractant selectivity for metal ions able to detect this type of pollutant. The solvent extraction properties of four acetyls, four methyl ketones and four benzoyls derivatives from azocalix[4]arenes which were prepared by linking 4-ethyl, 4-n-butyl, 4-acetamid anilin and 2-aminothiazol to calix[4]arene through a diazo-coupling reaction, the alkaline earth (Sr2+) and the transition (Ag+, Hg2+, Co2+, Ni2+, Cu2+, Zn2+, Cd2+, Cr3+) metal cations have been determined by extraction studies with metal picrates. Both ketones are better extractants than esters, and show a strong preference for Ag+, while Cu2+ and Cr3+ are the most extracted cation with the esters. Both acetyl and benzoyl esters are good carriers for Ag+ and Hg2+.

  11. Adsorption of iodine on silver wire

    International Nuclear Information System (INIS)

    It is an important process in which iodine is adsorbed on silver wire during the preparation of 125I seed sources. In this paper, a technique of adsorption of iodine on silver wire was studied. The influence of several factors, such as the type of reagent for halogenation, the time for halogenation, the time for adsorption, pH value, ion concentration, carrier iodine and so on, on the utilization rate of 131I was investigated, and the effectiveness of our proposed technique for adsorption of iodine on silver wire was confirmed. The procedure is summarized as follows: silver wire acidification: using 4 mol/L HNO3 as halogenation agent, stirring acidified for 20 min; silver wire halogenation: used 2 mol/L NaClO3 as halogenated agent, halogenation for 3 h; adsorption of iodine on silver wire: room temperature, pH value for the reaction is about 3, the time for adsorption is 30 min, carrier iodine is 27.5 μg. Original radioactivity of reaction solution was determined based on radioactivity of source-core that user required. (authors)

  12. [In vitro percutaneous absorption of silver nanoparticles].

    Science.gov (United States)

    Filon, F Larese; D'Agostin, F; Crosera, M; Adami, G; Rosani, R; Romano, C; Bovenzi, M; Maina, G

    2007-01-01

    There is a growing interest in the debate on nanoparticle safety for topical use. The benefits of nanoparticles have been shown in several scientific fields, but little is known about their potential to penetrate the skin lies. This study aims at evaluating in vitro silver nanoparticles skin penetration. Experiments were performed using the Franz diffusion cell method with intact and damaged human skin. Physiological solution was used as receiving phase and 70 microg/cm2 of silver nanoparticles dispersed in synthetic sweat were applied as donor phase to the outer surface of the skin for 24h. The receptor fluid measurements were performed by Electro Thermal Atomic Absorption Spectroscopy (ETAAS). Silver concentration of 0.2 microg/L was found in the receiving solutions of two cells, in which damaged skin membranes were set up. In the other tests, we obtained a silver concentration below the limit of detection in the receiving cells. Our experimental data show that silver nanoparticles permeation through intact and damaged skin is negligible. These findings are consistent with previously published results. Further researches are necessary to explore skin absorption of silver nanoparticles.

  13. Micro-CT imaging of denatured chitin by silver to explore honey bee and insect pathologies.

    Directory of Open Access Journals (Sweden)

    Peter R Butzloff

    Full Text Available BACKGROUND: Chitin and cuticle coatings are important to the environmental and immune defense of honey bees and insect pollinators. Pesticides or environmental effects may target the biochemistry of insect chitin and cuticle coating. Denaturing of chitin involves a combination of deacetylation, intercalation, oxidation, Schweiger-peeling, and the formation of amine hydrochloride salt. The term "denatured chitin" calls attention to structural and property changes to the internal membranes and external carapace of organisms so that some properties affecting biological activities are diminished. METHODOLOGY/PRINCIPAL FINDINGS: A case study was performed on honey bees using silver staining and microscopic computer-tomographic x-ray radiography (micro-CT. Silver nitrate formed counter-ion complexes with labile ammonium cations and reacted with amine hydrochloride. Silver was concentrated in the peritrophic membrane, on the abdomen, in the glossa, at intersegmental joints (tarsi, at wing attachments, and in tracheal air sacs. Imaged mono-esters and fatty acids from cuticle coating on external surfaces were apparently reduced by an alcohol pretreatment. CONCLUSIONS/SIGNIFICANCE: The technique provides 3-dimensional and sectional images of individual honey bees consistent with the chemistries of silver reaction and complex formation with denatured chitin. Environmental exposures and influences such as gaseous nitric oxide intercalant, trace oxidants such as ozone gas, oligosachharide salt conversion, exposure to acid rain, and chemical or biochemical denaturing by pesticides may be studied using this technique. Peritrophic membranes, which protect against food abrasion, microorganisms, and permit efficient digestion, were imaged. Apparent surface damage to the corneal lenses of compound eyes by dilute acid exposure consistent with chitin amine hydrochloride formation was imaged. The technique can contribute to existing insect pathology research, and may

  14. Structurally Distinct Cation Channelrhodopsins from Cryptophyte Algae.

    Science.gov (United States)

    Govorunova, Elena G; Sineshchekov, Oleg A; Spudich, John L

    2016-06-01

    Microbial rhodopsins are remarkable for the diversity of their functional mechanisms based on the same protein scaffold. A class of rhodopsins from cryptophyte algae show close sequence homology with haloarchaeal rhodopsin proton pumps rather than with previously known channelrhodopsins from chlorophyte (green) algae. In particular, both aspartate residues that occupy the positions of the chromophore Schiff base proton acceptor and donor, a hallmark of rhodopsin proton pumps, are conserved in these cryptophyte proteins. We expressed the corresponding polynucleotides in human embryonic kidney (HEK293) cells and studied electrogenic properties of the encoded proteins with whole-cell patch-clamp recording. Despite their lack of residues characteristic of the chlorophyte cation channels, these proteins are cation-conducting channelrhodopsins that carry out light-gated passive transport of Na(+) and H(+). These findings show that channel function in rhodopsins has evolved via multiple routes. PMID:27233115

  15. Radiation chemistry of aromatic dimer radical cations

    International Nuclear Information System (INIS)

    π-π Interactions of aromatic molecules are paid attention much in many fields, especially biology, chemistry, and applied physics, represented as protein, DNA, electron donor-accepter complexes, charge transfers, and self assembly molecules. Aromatic molecules including benzene rings are the simplest case to study the π-π interactions. To interpret the charge resonance (CR) structure in the dimer radical cations, spectroscopic and ESR methods have been carried out. The spectroscopic study on the dimer radical ion of molecules with two chromophores would be profitable to identify the electronic and configurational properties. In this article, dynamics of the dimer radical cation of benzenes, polystyrenes, and resist polymers is described on the basis of direct observation of CR band by the nanosecond pulse radiolysis and low temperature γ-radiolysis methods. (author)

  16. In situ Investigation of the Silver-CTAB system

    Energy Technology Data Exchange (ETDEWEB)

    Gray, J J; Orme, C A; Du, D; Srolovitz, D

    2007-04-16

    Recent research has shown that biologically inspired approaches to materials synthesis and self-assembly, hold promise of unprecedented atomic level control of structure and interfaces. In particular, the use of organic molecules to control the production of inorganic technological materials has the potential for controlling grain structure to enhance material strength; controlling facet expression for enhanced catalytic activity; and controlling the shape of nanostructured materials to optimize optical, electrical and magnetic properties. In this work, we use organic molecules to modify silver crystal shapes towards understanding the metal-organic interactions that lead to nanoparticle shape control. Using in situ electrochemical AFM (EC-AFM) as an in situ probe, we study the influence of a cationic surfactant cetyltrimethylamminobromide (CTAB) on Ag growth during electrochemical deposition on Ag(100). The results show that the organic surfactant promotes the growth of steps on the (100) surface and changes the surface evolution from island nucleation to step flow growth. Overall, this leads to a smoother, faster growing (100) surface, which may promote plate-formation.

  17. Alkaline earth cation extraction from acid solution

    Science.gov (United States)

    Dietz, Mark; Horwitz, E. Philip

    2003-01-01

    An extractant medium for extracting alkaline earth cations from an aqueous acidic sample solution is described as are a method and apparatus for using the same. The separation medium is free of diluent, free-flowing and particulate, and comprises a Crown ether that is a 4,4'(5')[C.sub.4 -C.sub.8 -alkylcyclohexano]18-Crown-6 dispersed on an inert substrate material.

  18. Cation Permeability in Soybean Aleurone Layer

    OpenAIRE

    Noda, Hiroko; Fukuda, Mitsuru

    1998-01-01

    The permeation of water and ions into bean seeds is essential for processing and cooking of beans. The permeability of cations, K, Na, Ca, and Mg ions, into soybean seed tissue, especially aleurone layer, during water uptake was investigated to characterize the ion permeation into soybeans. Aleurone layers and seed coats contained relatively high concentration of endogenous K and Ca ions, and endogenous Ca ion, respectively. The amounts of Ca ion entered seed coats and aleurone layers were gr...

  19. Controlled growth of large-scale silver nanowires

    Institute of Scientific and Technical Information of China (English)

    Xiao Cong-Wen; Yang Hai-Tao; Shen Cheng-Min; Li Zi-An; Zhang Huai-Ruo; Liu Fei; Yang Tian-Zhong; Chen Shu-Tang; Gao Hong-Jun

    2005-01-01

    Large-scale silver nanowires with controlled aspect ratio were synthesized via reducing silver nitrate with 1, 2-propanediol in the presence of poly (vinyl pyrrolidone) (PVP). Scanning electron microscopy, transmission electron microscopy and x-ray powder diffraction were employed to characterize these silver nanowires. The diameter of the silver nanowires can be readily controlled in the range of 100 to 400 nm by varying the experimental conditions. X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy results show that there exists no chemical bond between the silver and the nitrogen atoms. The interaction between PVP and silver nanowires is mainly through the oxygen atom in the carbonyl group.

  20. Partitional clustering algorithms

    CERN Document Server

    2015-01-01

    This book summarizes the state-of-the-art in partitional clustering. Clustering, the unsupervised classification of patterns into groups, is one of the most important tasks in exploratory data analysis. Primary goals of clustering include gaining insight into, classifying, and compressing data. Clustering has a long and rich history that spans a variety of scientific disciplines including anthropology, biology, medicine, psychology, statistics, mathematics, engineering, and computer science. As a result, numerous clustering algorithms have been proposed since the early 1950s. Among these algorithms, partitional (nonhierarchical) ones have found many applications, especially in engineering and computer science. This book provides coverage of consensus clustering, constrained clustering, large scale and/or high dimensional clustering, cluster validity, cluster visualization, and applications of clustering. Examines clustering as it applies to large and/or high-dimensional data sets commonly encountered in reali...

  1. Modernization typologies industrial clusters

    Directory of Open Access Journals (Sweden)

    Karapetian, Eduard

    2011-11-01

    Full Text Available Generalized theoretical approach to the criteria of industrial clusters. On this basis, a detailed typology of industrial cluster structures, which takes into account the peculiarities of the functioning of clusters in the domestic economy.

  2. UV Treatment of the Stabilizing Shell for Improving the Photostability of Silver Nanoparticles

    Directory of Open Access Journals (Sweden)

    Silvia Rinaldi

    2016-01-01

    Full Text Available Silver nanoparticles or nanoclusters are quite sensitive to light exposure. In particular, irradiation in the localized surface plasmon resonance (LSPR region brings about a drastic modification of their optical properties due to growth and reshaping of the nanoparticles. In order to obtain luminescent colloids, small silver colloidal nanoparticles were prepared in chloroform using vinylpyrrolidone oligomers as capping agent and their luminescence properties were used to control their stability upon prolonged exposure to visible light. The polymeric shell around the metal clusters was hardened through photo-cross-linking by UV light. This process did not alter the morphology and the optical properties of the nanoparticles but greatly improved the particle photostability as confirmed also by confocal laser scanning microscopy measurements. The data clearly show that UV curing of the stabilizing layer could be a simple postsynthetic procedure to obtain materials with stable properties.

  3. Gold Doping of Silver Nanoclusters: A 26-Fold Enhancement in the Luminescence Quantum Yield.

    Science.gov (United States)

    Soldan, Giada; Aljuhani, Maha A; Bootharaju, Megalamane S; AbdulHalim, Lina G; Parida, Manas R; Emwas, Abdul-Hamid; Mohammed, Omar F; Bakr, Osman M

    2016-05-01

    A high quantum yield (QY) of photoluminescence (PL) in nanomaterials is necessary for a wide range of applications. Unfortunately, the weak PL and moderate stability of atomically precise silver nanoclusters (NCs) suppress their utility. Herein, we accomplished a ≥26-fold PL QY enhancement of the Ag29 (BDT)12 (TPP)4 cluster (BDT: 1,3-benzenedithiol; TPP: triphenylphosphine) by doping with a discrete number of Au atoms, producing Ag29-x Aux (BDT)12 (TPP)4 , x=1-5. The Au-doped clusters exhibit an enhanced stability and an intense red emission around 660 nm. Single-crystal XRD, mass spectrometry, optical, and NMR spectroscopy shed light on the PL enhancement mechanism and the probable locations of the Au dopants within the cluster. PMID:27060602

  4. Antibacterial Properties and Mechanism of Activity of a Novel Silver-Stabilized Hydrogen Peroxide.

    Directory of Open Access Journals (Sweden)

    Nancy L Martin

    Full Text Available Huwa-San peroxide (hydrogen peroxide; HSP is a NSF Standard 60 (maximum 8 mg/L(-1 new generation peroxide stabilized with ionic silver suitable for continuous disinfection of potable water. Experiments were undertaken to examine the mechanism of HSP against planktonic and biofilm cultures of indicator bacterial strains. Contact/kill time (CT relationships that achieve effective control were explored to determine the potential utility in primary disinfection. Inhibitory assays were conducted using both nutrient rich media and a medium based on synthetic wastewater. Assays were compared for exposures to three disinfectants (HSP, laboratory grade hydrogen peroxide (HP and sodium hypochlorite at concentrations of 20 ppm (therefore at 2.5 and 5 times the NSF limit for HP and sodium hypochlorite, respectively and at pH 7.0 and 8.5 in dechlorinated tap water. HSP was found to be more or equally effective as hypochlorite or HP. Results from CT assays comparing HSP and HP at different bacterial concentrations with neutralization of residual peroxide with catalase suggested that at a high bacterial concentration HSP, but not HP, was protected from catalase degradation possibly through sequestration by bacterial cells. Consistent with this hypothesis, at a low bacterial cell density residual HSP was more effectively neutralized as less HSP was associated with bacteria and therefore accessible to catalase. Silver in HSP may facilitate this association through electrostatic interactions at the cell surface. This was supported by experiments where the addition of mono (K(+ and divalent (Ca(+2 cations (0.005-0.05M reduced the killing efficacy of HSP but not HP. Experiments designed to distinguish any inhibitory effect of silver from that of peroxide in HSP were carried out by monitoring the metabolic activity of established P. aeruginosa PAO1 biofilms. Concentrations of 70-500 ppm HSP had a pronounced effect on metabolic activity while the equivalent

  5. Preparation of sintered silver nanosheets by coating technique using silver carbamate complex

    Energy Technology Data Exchange (ETDEWEB)

    Ahn, Hee-Yong; Cha, Jae-Ryung; Gong, Myoung-Seon, E-mail: msgong@dankook.ac.kr

    2015-03-01

    This study describes a coating technique approach for large-scale preparation of sintered silver nanosheets whose lateral dimensions were controlled in the thickness range of 50–65 nm. These procedures involved coating water-soluble poly (vinyl alcohol) (PVA) and silver 2-ethylhexylcarbamate (Ag-EHC), as well as thermal reduction of a silver precursor by heating at 150 °C, followed by dissolving away the PVA layer with alcoholic water. When the silver carbamate layer on the PVA layer was heated to 150 °C, the silver carbamate layer was thermally reduced and directed to grow into uniform sintered nanosheets with aspect ratios as high as 1000. The multi-stacked PVA/Ag structures and sintered silver nanosheets were confirmed by scanning electron microscopy, energy dispersive spectroscopy, and X-ray diffraction. Measurements of the conductive property at room temperature indicated that these nanosheets were electrically continuous with a resistivity of approximately 7.3 × 10{sup −6} Ω cm. - Highlights: • A coating technique is used to make sintered Ag nanosheets. • PVA and silver carbamate act as a separation layer and a silver precursor. • The Ag nanosheets have thickness width 50–60 nm and width up to hundred μm. • The Ag nanosheets showed a resistivity of ca. 7.3 × 10{sup −6} Ω cm.

  6. Relaxation of the Silver/Silver Iodide Electrode in Aqueous Solution

    NARCIS (Netherlands)

    Peverelli, K.J.

    1979-01-01

    The aim of this study is to detect and characterize relaxation processes on silver/silver iodide electrodes in aqueous electrolyte solution. The information obtained is to be used for an estimation of the consequences of similar processes on colloidal AgI particles during encounter.In chapter 1 a ge

  7. Low cation coordination in oxide melts

    Energy Technology Data Exchange (ETDEWEB)

    Skinner, Lawrie [State University of New York, Stony Brook; Benmore, Chris J [Argonne National Laboratory (ANL); Du, Jincheng [University of North Texas; Weber, Richard [Argonne National Laboratory (ANL); Neuefeind, Joerg C [ORNL; Tumber, Sonia [Materials Development, Inc., Evanston, IL; Parise, John B [Stony Brook University (SUNY)

    2014-01-01

    The complete set of Faber-Ziman partial pair distribution functions for a rare earth oxide liquid were measured for the first time by combining aerodynamic levitation, neutron diffraction, high energy x-ray diffraction and isomorphic substitution using Y2 O3 and Ho2 O3 melts. The average Y- O coordination is measured to be 5.5(2), which is significantly less than the octahedral coordination of crystalline Y2 O3 (or Ho2 O3 ). Investigation of high temperature La2 O3 , ZrO2 , SiO2 , and Al2 O3 melts by x-ray diffraction and molecular dynamics simulations also show lower-than-crystal cation- oxygen coordination. These measurements suggest a general trend towards lower M-O coordination compared to their crystalline counterparts. It is found that this coordination number drop is larger for lower field strength, larger radius cations and is negligible for high field strength (network forming) cations. These findings have broad implications for predicting the local structure and related physical properties of metal-oxide melts and oxide glasses.

  8. Low Cation Coordination in Oxide Melts

    Science.gov (United States)

    Skinner, L. B.; Benmore, C. J.; Weber, J. K. R.; Du, J.; Neuefeind, J.; Tumber, S. K.; Parise, J. B.

    2014-04-01

    The complete set of partial pair distribution functions for a rare earth oxide liquid are measured by combining aerodynamic levitation, neutron and x-ray diffraction on Y2O3, and Ho2O3 melts at 2870 K. The average Y-O (or Ho-O) coordination of these isomorphic melts is measured to be 5.5(2), which is significantly less than the octahedral coordination of crystalline Y2O3 (or Ho2O3). Investigation of La2O3, ZrO2, and Al2O3 melts by x-ray diffraction and molecular dynamics simulations also show lower-than-crystal cation-oxygen coordination. These measurements suggest a general trend towards lower coordination compared to their crystalline counterparts. It is found that the coordination drop is larger for lower field strength, larger radius cations and is negligible for high field strength (network forming) cations, such as SiO2. These findings have broad implications for predicting the local structure and related physical properties of metal-oxide melts and oxide glasses.

  9. Limited data speaker identification

    Indian Academy of Sciences (India)

    H S Jayanna; S R Mahadeva Prasanna

    2010-10-01

    In this paper, the task of identifying the speaker using limited training and testing data is addressed. Speaker identification system is viewed as four stages namely, analysis, feature extraction, modelling and testing. The speaker identification performance depends on the techniques employed in these stages. As demonstrated by different experiments, in case of limited training and testing data condition, owing to less data, existing techniques in each stage will not provide good performance. This work demonstrates the following: multiple frame size and rate (MFSR) analysis provides improvement in the analysis stage, combination of mel frequency cepstral coefficients (MFCC), its temporal derivatives $(\\Delta,\\Delta \\Delta)$, linear prediction residual (LPR) and linear prediction residual phase (LPRP) features provides improvement in the feature extraction stage and combination of learning vector quantization (LVQ) and gaussian mixture model – universal background model (GMM–UBM) provides improvement in the modelling stage. The performance is further improved by integrating the proposed techniques at the respective stages and combining the evidences from them at the testing stage. To achieve this, we propose strength voting (SV), weighted borda count (WBC) and supporting systems (SS) as combining methods at the abstract, rank and measurement levels, respectively. Finally, the proposed hierarchical combination (HC) method integrating these three methods provides significant improvement in the performance. Based on these explorations, this work proposes a scheme for speaker identification under limited training and testing data.

  10. Entropy-Driven Clustering in Tetrahedrally Bonded Multinary Materials

    Science.gov (United States)

    Zawadzki, Paweł; Zakutayev, Andriy; Lany, Stephan

    2015-03-01

    Compositional inhomogeneities in multielemental materials typically form due to lowering of the energy relative to the homogeneous phase. Here, we demonstrate an entropy-driven mechanism in the zinc-blende derived cation-substituted multinary compounds Cu2SnS3 (CTS) and Cu2ZnSnS4 (CZTS). Using a motif-based model Hamiltonian and Monte Carlo simulations, we find that disorder leads to a redistribution of the structural motifs in such a way to create cation clustering. The associated formation of (sub-) nanometer-scale compositional inhomogeneities can cause potential fluctuations with detrimental consequences for photovoltaic applications.

  11. Orbital symmetry as a tool for understanding the bonding in Krossing's cation.

    Science.gov (United States)

    Deubel, Dirk V

    2002-10-16

    The geometric and electronic structure of Krossing's cation, Ag(eta(2)-P(4))(2)(+), which shows an unexpected planar coordination environment at the metal center and D(2)(h) symmetry both in solution and in the solid state, have been investigated using density functional theory and orbital-symmetry-based energy decomposition. The analysis reveals that the contribution from electrostatic interactions to the bond energy is greater than that of orbital interactions. Partitioning of the latter term into the irreducible representations shows that, in addition to the 5s orbital, 5p orbitals of silver act as acceptor orbitals for electron donation from sigma(P-P) orbitals (a(1)(g), b(1)(u)) and n(P) orbitals (b(3)(u)). Back-donation from the 4d(10) closed shell of Ag into sigma orbitals of the pnictogen cages (b(2)(g)) is also important. However, this contribution is shown not to determine the D(2)(h) structure, contradicting conclusions from the pioneering study of the title cation (J. Am. Chem.Soc. 2001, 123, 4603). The contributions from the irreducible representations to the stabilizing orbital interactions in the D(2)(h) structure and in its D(2)(d)-symmetric conformer are analogous, indicating that the planar coordination environment at the metal center in Ag(eta(2)-P(4))(2)(+) is induced by intermolecular rather than by intramolecular interactions. Because ethylene coordination to a metal ion is an elementary reaction step in industrial processes, the bonding in Ag(C(2)H(4))(2)(+) has been analyzed as well and compared to that in Krossing's cation. Surprisingly, similar contributions to the bond energies and an involvement of metal 4d and 5p orbitals have been found, whereas a recent atoms in molecules analysis suggested that the metal-ligand interactions in silver(I) olefin complexes fundamentally differ from those in tetrahedro P(4) complexes. The only qualitative difference between the bonding patterns in Ag(eta(2)-P(4))(2)(+) and Ag(C(2)H(4))(2)(+) is the

  12. A Mesoionic Carbene as Neutral Ligand for Phosphorescent Cationic Ir(III) Complexes.

    Science.gov (United States)

    Baschieri, Andrea; Monti, Filippo; Matteucci, Elia; Mazzanti, Andrea; Barbieri, Andrea; Armaroli, Nicola; Sambri, Letizia

    2016-08-15

    Two phosphorescent Ir(III) complexes bearing a mesoionic carbene ligand based on 1,2,3-triazolylidene are obtained for the first time. A silver-iridium transmetalation of the in situ-generated mesoionic carbene affords the cationic dichloro complex [Ir(trizpy)2Cl2](+) (3, trizpy = 1-benzyl-3-methyl-4-(pyridin-2-yl)-1H-1,2,3-triazolylidene) that reacts with a bis-tetrazolate (b-trz) dianionic ligand to give [Ir(trizpy)2(b-trz)](+) (5). The new compounds are fully characterized by NMR spectroscopy and mass spectrometry, and the X-ray structure of 3 is determined. The electrochemical behavior is somewhat different compared to most standard cationic iridium complexes. The first oxidation process is shifted to substantially higher potential in both 3 and 5, due to peculiar and different ligand-induced effects in the two cases, which stabilize the highest occupied molecular orbital; reduction processes are centered on the mesoionic carbene ligands. Both compounds exhibit a mostly ligand-centered luminescence band in the blue-green spectral region, substantially stronger in the case of 5 versus 3, both in CH3CN solution and in poly(methyl methacrylate) matrix at room temperature. Optimized geometries, orbital energies, spin densities, and electronic transitions are determined via density functional theory calculations, which support a full rationalization of the electrochemical and photophysical behavior. This work paves the way for the development of Ir-based emitters with neutral mesoionic carbene ligands and anionic ancillary ligands, a new concept in the area of cationic Ir(III) complexes. PMID:27483041

  13. Silver nanoparticles from silver halide photography to plasmonics

    CERN Document Server

    Tani, Tadaaki

    2015-01-01

    This book provides systematic knowledge and ideas on nanoparticles of Ag and related materials. While Ag and metal nanoparticles are essential for plasmonics, silver halide (AgX) photography relies to a great extent on nanoparticles of Ag and AgX which have the same crystal structure and have been studied extensively for many years. This book has been written to combine the knowledge of nanoparticles of Ag and related materials in plasmonics and AgX photography in order to provide new ideas for metal nanoparticles in plasmonics. Chapters 1–3 of this book describe the structure and formation of nanoparticles of Ag and related materials. Systematic descriptions of the structure and preparation of Ag, Au, and noble-metal nanoparticles for plasmonics are followed by and related to those of nanoparticles of Ag and AgX in AgX photography. Knowledge of the structure and preparation of Ag and AgX nanoparticles in photography covers nanoparticles with widely varying sizes, shapes, and structures, and formation proce...

  14. Separation of silver from silver-manganese ore with cellulose as reductant

    Institute of Scientific and Technical Information of China (English)

    ZHANG Xiao-yun; TIAN Xue-da; ZHANG Dong-fang

    2006-01-01

    The silver in some silver-manganese ore with a grade of 3.15 × 10-4 was concentrated by a combined beneficiation technique including magnetic separation, flotation, reducing leaching and gravity desliming. The major silver contained in manganese ore as isomorphism was concentrated by magnetic separation, while around 8.50% of the silver individual minerals were separated by flotation. The manganese in the mixed concentrate of both magnetic separation and flotation was dissolved in a reducing leaching, in which some cellulose reductant named CMK was used. Part of the slime contained in leach residue was removed by a laboratory desliming equipment. A silver concentrate with a grade of 4.96 × 10-3 Ag and a recovery of 84.25% were obtained.

  15. Application of Extended Smoluchowski Equations to Formation of Silver Nanoclusters Generated by Direct Current Magnetron Sputtering Source

    Science.gov (United States)

    Zhang, Chuhang; Feng, Yuanxin

    2016-09-01

    We apply the extended Smoluchowski rate equations with neutralization process between nanocluster (NC) anion and cation to study the formation of silver NCs generated by direct current magnetron sputtering (DC-MSP). By comparing the experimental and simulation results, it was found that the origin of size tuning by the cell length was prolonged aggregation time. Size tuning by DC power (P) was attributed to the enhanced initial number density and ionization fraction of the sputtered materials. It was revealed that parts of NC ions were "lost" after aggregation and the amount of lost ions increased with power (20 W gas phase.

  16. 生物法制备纳米银溶胶的稳定性%Stability of Colloidal Silver Nanoparticles Prepared by Bioreduction

    Institute of Scientific and Technical Information of China (English)

    孙道华; 李清彪; 何宁; 黄加乐; 王惠璇

    2011-01-01

    利用生物还原法制备纳米银溶胶,借助于UV-Vis表征技术对其热稳定性和化学稳定性进行考察.结果表明:生物法制备的纳米银溶胶在100℃下加热6 h,UV-Vis谱图未发生明显变化;H+和具有高价阳离子的电解质对其稳定性的影响明显;OH-对银溶胶的稳定性影响相对较弱.生物法制备的纳米银溶胶在热稳定性、化学稳定性方面均略优于柠檬酸三钠法制得的银溶胶.%The thermal and chemical statoilities of the colloid silver nanoparticles prepared by bioreduction were investigated in virtue of UV-Vis spectrometer.The results indicate that UV-Vis spectra of silver colloid prepared by bioreduction have not significant change after heat treatment at 100 ℃ for 6 h.Hydrogen ion and the electrolyte with multivalent cation markedly influence stabilities of the silver colloid, while hydroxide anion has a weak influence on its stability.Thermal and chemical stabilities of the silver colloid prepared by bioreduction are superior to that of the silver colloid prepared by the sodium citrate reduction method.

  17. Silver nanoparticles incorporated onto ordered mesoporous silica from Tollen's reagent

    Science.gov (United States)

    Zienkiewicz-Strzałka, M.; Pasieczna-Patkowska, S.; Kozak, M.; Pikus, S.

    2013-02-01

    Noble metal nanostructures supported on mesoporous silica are bridge between traditional silica adsorbents and modern catalysts. In this work the Ag/SBA-15 mesoporous materials were synthesized and characterized. Various forms of nanosilver supported on ordered mesoporous template have been successfully obtained via proposed procedures. In all synthesized materials, Tollen's reagent (diammine silver complex [Ag(NH3)2]+) was used as a silver source. Silver nanoparticles were prepared by reduction of ammoniacal silver complex by formaldehyde in the solution of stabilizer. After reduction, Ag nanoparticles could be deposited on SBA-15, or added during traditional synthesis of SBA-15 giving silver or silver chloride nanoparticles in the combination with porous silica. Silver nanostructures as nanoparticles or nanowires were also embedded onto the SBA-15 by incipient wetness impregnation of silver ions. Absorbed silver ions were next reduced under hydrogen at high temperature. There are many advantages of utilized ammoniacal silver complex as a silver source. Proposed method is capable to synthesis of various metal nanostructures with controlled composition and morphology. The silver ammonia complex is composed of two ions surrounding and protecting the central silver ion, so it is possible to obtain very small nanoparticles using simple approach without any functionalization of external and internal surface of SBA-15. This approach allows obtaining greatly small silver nanoparticles on SBA-15 (4 nm) or nanowires depending on the metal loading amount. Moreover, the colloidal silver solution prepared from Tollen's reagent, in the presence of triblock copolymer, remains stable for a long time. Reduction of Tollen's reagent to silver colloidal solution seems to be efficient, fast and interesting approach for the preparation of supported silver nanostructures Obtained samples were characterized by powder X-ray diffraction, small angle X-ray scattering (SAXS), UV

  18. Glass frits coated with silver nanoparticles for silicon solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Li, Yingfen, E-mail: lyf350857423@163.com; Gan, Weiping; Zhou, Jian; Li, Biyuan

    2015-06-30

    Graphical abstract: - Highlights: • Silver-coated glass frits for solar cells were prepared by electroless plating. • Gum Arabic was used as the activating agent of glass frits. • Silver-coated glass frits can improve the photovoltaic performances of solar cells. - Abstract: Glass frits coated with silver nanoparticles were prepared by electroless plating. Gum Arabic (GA) was used as the activating agent of glass frits without the assistance of stannous chloride or palladium chloride. The silver-coated glass frits prepared with different GA dosages were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), and thermogravimetric analysis (TGA). The characterization results indicated that silver-coated glass frits had the structures of both glass and silver. Spherical silver nanoparticles were distributed on the glass frits evenly. The density and particle size of silver nanoparticles on the glass frits can be controlled by adjusting the GA dosage. The silver-coated glass frits were applied to silver pastes to act as both the densification promoter and silver crystallite formation aid in the silver electrodes. The prepared silver-coated glass frits can improve the photovoltaic performances of solar cells.

  19. Silver, gold, and alloyed silver-gold nanoparticles: characterization and comparative cell-biologic action

    Energy Technology Data Exchange (ETDEWEB)

    Mahl, Dirk; Diendorf, Joerg; Ristig, Simon [University of Duisburg-Essen, Department of Inorganic Chemistry, Center for Nanointegration Duisburg-Essen (CeNIDE) (Germany); Greulich, Christina [Ruhr-University of Bochum, Bergmannsheil University Hospital/Surgical Research (Germany); Li Zian; Farle, Michael [University of Duisburg-Essen, Faculty of Physics, Center for Nanointegration Duisburg-Essen (CeNIDE) (Germany); Koeller, Manfred [Ruhr-University of Bochum, Bergmannsheil University Hospital/Surgical Research (Germany); Epple, Matthias, E-mail: matthias.epple@uni-due.de [University of Duisburg-Essen, Department of Inorganic Chemistry, Center for Nanointegration Duisburg-Essen (CeNIDE) (Germany)

    2012-10-15

    Silver, gold, and silver-gold-alloy nanoparticles were prepared by citrate reduction modified by the addition of tannin during the synthesis, leading to a reduction in particle size by a factor of three. Nanoparticles can be prepared by this easy water-based synthesis and subsequently functionalized by the addition of either tris(3-sulfonatophenyl)phosphine or poly(N-vinylpyrrolidone). The resulting nanoparticles of silver (diameter 15-25 nm), gold (5-6 nm), and silver-gold (50:50; 10-12 nm) were easily dispersable in water and also in cell culture media (RPMI + 10 % fetal calf serum), as shown by nanoparticle tracking analysis and differential centrifugal sedimentation. High-resolution transmission electron microscopy showed a polycrystalline nature of all nanoparticles. EDX on single silver-gold nanoparticles indicated that the concentration of gold is higher inside a nanoparticle. The biologic action of the nanoparticles toward human mesenchymal stem cells (hMSC) was different: Silver nanoparticles showed a significant concentration-dependent influence on the viability of hMSC. Gold nanoparticles showed only a small effect on the viability of hMSC after 7 days. Surprisingly, silver-gold nanoparticles had no significant influence on the viability of hMSC despite the silver content. Silver nanoparticles and silver-gold nanoparticles in the concentration range of 5-20 {mu}g mL{sup -1} induced the activation of hMSC as indicated by the release of IL-8. In contrast, gold nanoparticles led to a reduction of the release of IL-6 and IL-8.

  20. Alkali cation specific adsorption onto fcc(111) transition metal electrodes.

    Science.gov (United States)

    Mills, J N; McCrum, I T; Janik, M J

    2014-07-21

    The presence of alkali cations in electrolyte solutions is known to impact the rate of electrocatalytic reactions, though the mechanism of such impact is not conclusively determined. We use density functional theory (DFT) to examine the specific adsorption of alkali cations to fcc(111) electrode surfaces, as specific adsorption may block catalyst sites or otherwise impact surface catalytic chemistry. Solvation of the cation-metal surface structure was investigated using explicit water models. Computed equilibrium potentials for alkali cation adsorption suggest that alkali and alkaline earth cations will specifically adsorb onto Pt(111) and Pd(111) surfaces in the potential range of hydrogen oxidation and hydrogen evolution catalysis in alkaline solutions.

  1. Cation distribution and mixing thermodynamics in Fe/Ni thiospinels

    Science.gov (United States)

    Haider, Saima; Grau-Crespo, Ricardo; Devey, Antony J.; de Leeuw, Nora H.

    2012-07-01

    The structural analogy between Ni-doped greigite minerals (Fe3S4) and the (Fe, Ni)S clusters present in biological enzymes has led to suggestions that these minerals could have acted as catalysts for the origin of life. However, little is known about the distribution and stability of Ni dopants in the greigite structure. We present here a theoretical investigation of mixed thiospinels (Fe1-xNix)3S4, using a combination of density functional theory (DFT) calculations and Monte Carlo simulations. We find that the equilibrium distribution of the cations deviates significantly from a random distribution: at low Ni concentrations, Ni dopants are preferably located in octahedral sites, while at higher Ni concentrations the tetrahedral sites become much more favourable. The thermodynamic mixing behaviour between greigite and polydymite (Ni3S4) is dominated by the stability field of violarite (FeNi2S4), for which the mixing enthalpy exhibits a deep negative minimum. The analysis of the free energy of mixing shows that Ni doping of greigite is very unstable with respect to the formation of a separate violarite phase. The calculated variation of the cubic cell parameter with composition is found to be non-linear, exhibiting significant deviation from Vegard’s law, but in agreement with experiment.

  2. Factorial PD-Clustering

    CERN Document Server

    Tortora, Cristina; Summa, Mireille Gettler

    2011-01-01

    Factorial clustering methods have been developed in recent years thanks to the improving of computational power. These methods perform a linear transformation of data and a clustering on transformed data optimizing a common criterion. Factorial PD-clustering is based on Probabilistic Distance clustering (PD-clustering). PD-clustering is an iterative, distribution free, probabilistic, clustering method. Factorial PD-clustering make a linear transformation of original variables into a reduced number of orthogonal ones using a common criterion with PD-Clustering. It is demonstrated that Tucker 3 decomposition allows to obtain this transformation. Factorial PD-clustering makes alternatively a Tucker 3 decomposition and a PD-clustering on transformed data until convergence. This method could significantly improve the algorithm performance and allows to work with large dataset, to improve the stability and the robustness of the method.

  3. Small angle neutron scattering studies on the interaction of cationic surfactants with bovine serum albumin

    Indian Academy of Sciences (India)

    Nuzhat Gull; S Chodankar; V K Aswal; Kabir-Ud-Din

    2008-11-01

    The structure of the protein–surfactant complex of bovine serum albumin (BSA) and cationic surfactants has been studied by small angle neutron scattering. At low concentrations, the CTAB monomers are observed to bind to the protein leading to an increase in its size. On the other hand at high concentrations, surfactant molecules aggregate along the unfolded polypeptide chain of the protein resulting in the formation of a fractal structure representing a necklace model of micelle-like clusters randomly distributed along the polypeptide chain. The fractal dimension as well as the size and number of micelles attached to the complex have been determined.

  4. Nanostructured silver and platinum modified carbon fiber microelectrodes coated with nafion for H2O2 determination

    OpenAIRE

    Vladimir Halouzka; Petr Jakubec; Cenek Gregor; Dalibor Jancik; Gabriela Valaskova; Kyriakos Papadopoulos; Theodor Triantis; Jan Hrbac

    2010-01-01

    Carbon fiber microelectrodes equipped with nanostructured metals(platinum and silver) and covered with a Nafion layer constitutesensitive H2O2 sensors. Metallic layers on carbon fibers wereprepared by surfactant assisted electrodeposition. In the case ofsilver, the procedure leads to coating which is composed of porous,partially aggregated and crystalline deposits containing silvernanoparticles. The electrodeposition of platinum leads to carbonfiber decorated with clusters of platinum nanopar...

  5. Silver and Co-Ni sulphoarsenides from the Kongsberg silver deposit, Norway

    Science.gov (United States)

    Kullerud, Kåre; Kotková, Jana; Škoda, Radek

    2015-04-01

    The historical silver mines at Kongsberg, Norway, are world-famous for spectacular samples of thread silver exhibited at numerous mineralogical museums. More than 100 minerals have been reported from the deposit, including native elements (Ag, Au, As, Cu, S, C), sulphides, sulphosalts, selenides, arsenides, carbonates, sulphates, arsenates and halides, in addition to a range of silicate minerals (Neumann, 1944; Johnsen, 1986, 1987; Bancroft et al., 2001). However, documentation of the minerals using state-of-the-art methods such as electron microprobe, with implications for the genesis of the deposit, is largely missing. In our contribution, we present new data on the compositional variations of silver and sulphoarsenides from the silver deposit. Most of the ore minerals studied here occur in calcite veins in the hosting gneiss. For some samples, however, fluorite is the dominating vein mineral associated with the ore minerals. Mineral textures show that native silver formed during at least two separate stages. The earliest generation of native silver is typically represented by euhedral to subhedral crystals, up to 1 mm long. These crystals frequently contain rounded inclusions of acanthite, chalcopyrite and polybasite, and they are commonly rimmed by a zone consisting of Co-Ni-Fe bearing sulphoarsenides. The later generation of native silver occurs as fracture fillings, often enclosing the earlier Ag generation with its rim of sulphoarsenides. Native silver shows significant variations in Hg, Au and Sb contents. Concentrations of up to 20 wt% Hg and up to 2.7 wt% Sb in silver have been measured during the present study. Dyscrasite and allargentum have also been observed in association with native silver. Neumann (1944) reported auriferous silver with up to 50 % Au. The sulphoarsenides rimming the crystals of the first silver generation vary in composition along the cobaltite-gersdorffite series with approximate limiting compositions Ni0.8Fe0.2AsS and Co0.51Ni0

  6. Possibilistic Exponential Fuzzy Clustering

    Institute of Scientific and Technical Information of China (English)

    Kiatichai Treerattanapitak; Chuleerat Jaruskulchai

    2013-01-01

    Generally,abnormal points (noise and outliers) cause cluster analysis to produce low accuracy especially in fuzzy clustering.These data not only stay in clusters but also deviate the centroids from their true positions.Traditional fuzzy clustering like Fuzzy C-Means (FCM) always assigns data to all clusters which is not reasonable in some circumstances.By reformulating objective function in exponential equation,the algorithm aggressively selects data into the clusters.However noisy data and outliers cannot be properly handled by clustering process therefore they are forced to be included in a cluster because of a general probabilistic constraint that the sum of the membership degrees across all clusters is one.In order to improve this weakness,possibilistic approach relaxes this condition to improve membership assignment.Nevertheless,possibilistic clustering algorithms generally suffer from coincident clusters because their membership equations ignore the distance to other clusters.Although there are some possibilistic clustering approaches that do not generate coincident clusters,most of them require the right combination of multiple parameters for the algorithms to work.In this paper,we theoretically study Possibilistic Exponential Fuzzy Clustering (PXFCM) that integrates possibilistic approach with exponential fuzzy clustering.PXFCM has only one parameter and not only partitions the data but also filters noisy data or detects them as outliers.The comprehensive experiments show that PXFCM produces high accuracy in both clustering results and outlier detection without generating coincident problems.

  7. Silver nanowire decorated heatable textiles.

    Science.gov (United States)

    Doganay, Doga; Coskun, Sahin; Genlik, Sevim Polat; Unalan, Husnu Emrah

    2016-10-28

    The modification of insulating fabrics with electrically conductive nanomaterials has opened up a novel application field. With the help of Joule heating mechanism, conductive fabrics can be used as mobile heaters. In this work, heatable textiles are fabricated using silver nanowires (Ag NWs). Cotton fabrics are decorated with polyol synthesized Ag NWs via a simple dip-and-dry method. The time-dependent thermal response of the fabrics under different applied voltages is investigated. It is found that the fabrics can be heated to 50 °C under an applied power density of as low as 0.05 W cm(-2). Uniform deposition of Ag NWs resulted in the homogeneous generation of heat. In addition, the stability of the fabrics with time and under different bending and washing conditions is examined. Moreover, a simple control circuit is fabricated and integrated in order to demonstrate the high potential of the fabrics for mobile applications. This work provides a roadmap for researchers who would like to work on heatable textiles with metallic NWs. PMID:27651222

  8. Silver Nanoparticles and Mitochondrial Interaction

    Directory of Open Access Journals (Sweden)

    Eriberto Bressan

    2013-01-01

    Full Text Available Nanotechnology has gone through a period of rapid growth, thus leading to the constant increase in the application of engineered nanomaterials in daily life. Several different types of nanoparticles have been engineered to be employed in a wide array of applications due to their high surface to volume ratio that leads to unique physical and chemical properties. So far, silver nanoparticles (AgNps have been used in many more different medical devices than any other nanomaterial, mainly due to their antimicrobial properties. Despite the promising advantages posed by using AgNps in medical applications, the possible health effects associated with the inevitable human exposure to AgNps have raised concerns as to their use since a clear understanding of their specific interaction with biological systems has not been attained yet. In light of such consideration, aim of the present work is the morphological analysis of the intracellular behavior of AgNps with a diameter of 10 nm, with a special attention to their interaction with mitochondria.

  9. Transparent conducting silver nanowire networks

    CERN Document Server

    van de Groep, Jorik; Polman, Albert; 10.1021/nl301045a

    2013-01-01

    We present a transparent conducting electrode composed of a periodic two-dimensional network of silver nanowires. Networks of Ag nanowires are made with wire diameters of 45-110 nm and pitch of 500, 700 and 1000 nm. Anomalous optical transmission is observed, with an averaged transmission up to 91% for the best transmitting network and sheet resistances as low as 6.5 {\\Omega}/sq for the best conducting network. Our most dilute networks show lower sheet resistance and higher optical transmittance than an 80 nm thick layer of ITO sputtered on glass. By comparing measurements and simulations we identify four distinct physical phenomena that govern the transmission of light through the networks: all related to the excitation of localized surface plasmons and surface plasmon polaritons on the wires. The insights given in this paper provide the key guidelines for designing high-transmittance and low-resistance nanowire electrodes for optoelectronic devices, including thin-film solar cells. For these latter, we disc...

  10. In vitro percutaneous penetration and characterization of silver from silver-containing textiles

    Directory of Open Access Journals (Sweden)

    Bianco C

    2015-03-01

    Full Text Available Carlotta Bianco,1 Sanja Kezic,2 Matteo Crosera,1 Vesna Svetličić,3 Suzana Šegota,3 Giovanni Maina,4 Canzio Romano,5 Francesca Larese,6,7 Gianpiero Adami11Department of Chemical and Pharmaceutical Sciences, University of Trieste, Trieste, Italy; 2Academic Medical Center, Coronel Institute, University of Amsterdam, Amsterdam, the Netherlands; 3Laboratory for Bioelectrochemistry and Surface Imaging, Division for Marine and Environmental Research, Ruder Boškovic Institute, Zagreb, Croatia; 4Department of Clinical and Biological Sciences, University of Turin, Turin, Italy; 5Department of Public and Pediatric Health Sciences, University of Turin, Turin, Italy; 6Unit of Occupational Medicine, University of Trieste, Trieste, Italy; 7Department of Medical Sciences, University of Trieste, Trieste, ItalyAbstract: The objective of this study was to determine the in vitro percutaneous penetration of silver and characterize the silver species released from textiles in different layers of full thickness human skin. For this purpose, two different wound dressings and a garment soaked in artificial sweat were placed in the donor compartments of Franz cells for 24 hours. The concentration of silver in the donor phase and in the skin was determined by an electrothermal atomic absorption spectrometer (ET-AAS and by inductively coupled plasma mass spectrometer (ICP-MS. The characterization of silver species in the textiles and in the skin layers was made by scanning electron microscopy with integrated energy dispersive X-ray spectroscopy (SEM-EDX. Additionally, the size distribution of silver nanoparticles in the textiles was performed by atomic force microscopy (AFM. On the surface of all investigated materials, silver nanoparticles of different size and morphology were found. Released silver concentrations in the soaking solutions (ie, exposure concentration ranged from 0.7 to 4.7 µg/mL (0.6–4.0 µg/cm2, fitting the bactericidal range. Silver and silver

  11. Use of ferricyanide for gold and silver cyanidation

    Institute of Scientific and Technical Information of China (English)

    F. XIE; D. B. DREISINGER

    2009-01-01

    Low gold and silver leaching kinetics has been commonly observed in traditional gold-silver cyanidation process, especially in heap leaching and in situ leaching operations. The different mineralogy of gold and silver in the ores is suspected to be the main reason, e.g., the occurrence of low solubility acanthite (Ag2S) typically results in low overall silver extraction. Due to the low solubility of oxygen in cyanide solution, the reactivity and availability of oxidant is believed to be the critical limitation for gold and silver dissolution. The use of ferricyanide as the auxiliary oxidant for gold and silver cyanidation has been examined. The rotating disc test results prove the assistant effect of ferricyanide on increasing the dissolution rate of gold and silver. The potential use of ferricyanide in gold/silver cyanidation process is proposed based on the leaching results of actual ores.

  12. Sintered silver joints via controlled topography of electronic packaging subcomponents

    Science.gov (United States)

    Wereszczak, Andrew A.

    2014-09-02

    Disclosed are sintered silver bonded electronic package subcomponents and methods for making the same. Embodiments of the sintered silver bonded EPSs include topography modification of one or more metal surfaces of semiconductor devices bonded together by the sintered silver joint. The sintered silver bonded EPSs include a first semiconductor device having a first metal surface, the first metal surface having a modified topography that has been chemically etched, grit blasted, uniaxial ground and/or grid sliced connected to a second semiconductor device which may also include a first metal surface with a modified topography, a silver plating layer on the first metal surface of the first semiconductor device and a silver plating layer on the first metal surface of the second semiconductor device and a sintered silver joint between the silver plating layers of the first and second semiconductor devices which bonds the first semiconductor device to the second semiconductor device.

  13. Ink composition for making a conductive silver structure

    Energy Technology Data Exchange (ETDEWEB)

    Walker, Steven B.; Lewis, Jennifer A.

    2016-10-18

    An ink composition for making a conductive silver structure comprises a silver salt and a complex of (a) a complexing agent and a short chain carboxylic acid or (b) a complexing agent and a salt of a short chain carboxylic acid, according to one embodiment. A method for making a silver structure entails combining a silver salt and a complexing agent, and then adding a short chain carboxylic acid or a salt of the short chain carboxylic acid to the combined silver salt and a complexing agent to form an ink composition. A concentration of the complexing agent in the ink composition is reduced to form a concentrated formulation, and the silver salt is reduced to form a conductive silver structure, where the concentrated formulation and the conductive silver structure are formed at a temperature of about 120.degree. C. or less.

  14. Cytotoxicity and genotoxicity of biogenic silver nanoparticles

    Science.gov (United States)

    Lima, R.; Feitosa, L. O.; Ballottin, D.; Marcato, P. D.; Tasic, L.; Durán, N.

    2013-04-01

    Biogenic silver nanoparticles with 40.3 ± 3.5 nm size and negative surface charge (- 40 mV) were prepared with Fusarium oxysporum. The cytotoxicity of 3T3 cell and human lymphocyte were studied by a TaliTM image-based cytometer and the genotoxicity through Allium cepa and comet assay. The results of BioAg-w (washed) and BioAg-nw (unwashed) biogenic silver nanoparticles showed cytotoxicity exceeding 50 μg/mL with no significant differences of response in 5 and 10 μg/mL regarding viability. Results of genotoxicity at concentrations 5.0 and 10.0 ug/mL show some response, but at concentrations 0.5 and 1.0 μg/mL the washed and unwashed silver nanoparticles did not present any effect. This in an important result since in tests with different bacteria species and strains, including resistant, MIC (minimal inhibitory concentration) had good answers at concentrations less than 1.9 μg/mL. This work concludes that biogenic silver nanoparticles may be a promising option for antimicrobial use in the range where no cyto or genotoxic effect were observed. Furthermore, human cells were found to have a greater resistance to the toxic effects of silver nanoparticles in comparison with other cells.

  15. Characterization of antibacterial silver coated yarns.

    Science.gov (United States)

    Pollini, M; Russo, M; Licciulli, A; Sannino, A; Maffezzoli, A

    2009-11-01

    Surface treatments of textile fibers and fabrics significantly increase their performances for specific biomedical applications. Nowadays, silver is the most used antibacterial agent with a number of advantages. Among them, it is worth to note the high degree of biocompatibility, an excellent resistance to sterilization conditions, antibacterial properties with respect to different bacteria associated with a long-term of antibacterial efficiency. However, there are only a few antibacterial fibres available, mainly synthetic with high production cost and limited effectiveness. Cotton yarns with antimicrobial properties are most suitable for wound healing applications and other medical treatments thanks to their excellent moisture absorbance while synthetic based fibres are most suitable for industrial applications such as automotive tapestry and air filters. The silver-coated fibers were developed applying an innovative and low cost silver deposition technique for natural and synthetic fibers or yarns. The structure and morphology of the silver nanoclusters on the fibers was observed by scanning electron microscopy (SEM), atomic force microscopy analysis (AFM) and XRD analysis, and quantitatively confirmed by thermogravimetric analysis (TGA) measurements. Good silver coating stability has been confirmed performing several industrial washing. Antimicrobial tests with Escherichia coli were performed. PMID:19526328

  16. In situ SU-8 silver nanocomposites

    Directory of Open Access Journals (Sweden)

    Søren V. Fischer

    2015-07-01

    Full Text Available Nanocomposite materials containing metal nanoparticles are of considerable interest in photonics and optoelectronics applications. However, device fabrication of such materials always encounters the challenge of incorporation of preformed nanoparticles into photoresist materials. As a solution to this problem, an easy new method of fabricating silver nanocomposites by an in situ reduction of precursors within the epoxy-based photoresist SU-8 has been developed. AgNO3 dissolved in acetonitrile and mixed with the epoxy-based photoresist SU-8 forms silver nanoparticles primarily during the pre- and post-exposure soft bake steps at 95 °C. A further high-temperature treatment at 300 °C resulted in the formation of densely homogeneously distributed silver nanoparticles in the photoresist matrix. No particle growth or agglomeration of nanoparticles is observed at this point. The reported new in situ silver nanocomposite materials can be spin coated as homogeneous thin films and structured by using UV lithography. A resolution of 5 µm is achieved in the lithographic process. The UV exposure time is found to be independent of the nanoparticle concentration. The fabricated silver nanocomposites exhibit high plasmonic responses suitable for the development of new optoelectronic and optical sensing devices.

  17. The Antimicrobial Action of Silver Halides in Calcium Phosphate

    OpenAIRE

    Kalniņa, D; Gross, K; Onufrijevs, P.; Daukšta, E; Nikolajeva, V; Stankeviciute, Z; Kareiva, A.

    2015-01-01

    Silver halides represent a yet unexplored avenue for imparting antimicrobial activity to calcium phosphates. Negtively charged silver halide colloids (AgI, AgBr and AgCl) were added to synthesized amorphous calcium phosphate. Concurrent melting of silver halides and crystallization to carbonated apatite at 700 oC increased the silver halide surface area available to bacteria and formed a lower solubility apatite. The effect of the matrix solubility on antimicrobial response could ...

  18. SURFACE ENHANCED RAMAN SPECTRA FROM OXYGEN ON SILVER

    OpenAIRE

    Pettenkofer, C.; Pockrand, I.; Otto, A.

    1983-01-01

    Silver is an important catalyst for the epoxidation of ethylene and the production of formaldehyd from methanol. It is not yet known with certainty which form of adsorbed oxygen on silver is the catalytically active one. Therefore we have started to study the adsorption of oxygen on silver films by Raman spectroscopy. From previous investigations, especially from UPS work /1/, we know that at low exposures of ground state molecular oxygen, oxygen sticks on evaporated silver films only at defe...

  19. Nanoscale characterization of thin immersion silver coatings on copper substrates

    OpenAIRE

    Török, T. I.; Csik, A.; Hakl, J.; Vad, K.; KÖvÉr, L.; Tóth, J.; Mészáros, S.; Kun, É.; Sós, D.

    2015-01-01

    Microelectronic-grade copper foils were immersion silver plated in a home-made non-cyanide alkaline silver nitrate - thiosulfate solution and in two commercially available industrial baths via contact reductive precipitation. The concentration depth profiles of the freshly deposited silver layers were afterwards analyzed at nanoscale resolution by means of Secondary Neutral Mass Spectrometry (SNMS) and Glow Discharge Optical Emission Spectroscopy (GDOES). The thickness of deposited silver lay...

  20. Morphology and mechanical properties of antimicrobial polyamide/silver composites

    OpenAIRE

    Radheshkumar, C.; Münstedt, Helmut

    2005-01-01

    Silver filled antimicrobial polymers were produced from composites comprising polyamide and elementary silver powder possessing various specific surface area (SSA) by melt compounding. Different concentrations (2%, 4% and 8%) of the silver powder were incorporated in the polyamide to investigate the effect of silver loading on the mechanical properties. As the water uptake imparts antimicrobial properties, the influence of the diffused water on the mechanical properties of the compos...

  1. Management of cluster headache

    DEFF Research Database (Denmark)

    Tfelt-Hansen, Peer C; Jensen, Rigmor H

    2012-01-01

    and agitation. Patients may have up to eight attacks per day. Episodic cluster headache (ECH) occurs in clusters of weeks to months duration, whereas chronic cluster headache (CCH) attacks occur for more than 1 year without remissions. Management of cluster headache is divided into acute attack treatment...

  2. Structures of Mn clusters

    Indian Academy of Sciences (India)

    Tina M Briere; Marcel H F Sluiter; Vijay Kumar; Yoshiyuki Kawazoe

    2003-01-01

    The geometries of several Mn clusters in the size range Mn13–Mn23 are studied via the generalized gradient approximation to density functional theory. For the 13- and 19-atom clusters, the icosahedral structures are found to be most stable, while for the 15-atom cluster, the bcc structure is more favoured. The clusters show ferrimagnetic spin configurations.

  3. Ground-based Investigations of Atomic Oxygen Erosion Behaviors of Silver and Ion-implanted Silver

    Institute of Scientific and Technical Information of China (English)

    DUO Shu-wang; LI Mei-shuan; YIN Xiao-hui; LI Wen-kui; LI Ming-sheng

    2006-01-01

    Silver foils and ion-implanted silver foils exposed to atomic oxygen (AO) generated in a ground simulation facility were investigated by the quartz crystal microbalance (QCM), the scanning electron microscopy (SEM) and the X-ray photoelectron spectroscopy (XPS). The experimental results show the presence of Ag2O and AgO in an oxidation process of the silver foil having exposure to AO. As soon as silver comes under the bombardment of atomic oxygen, the oxidation process starts with a thick film forming on the silver surface. Because of the development of stresses, the oxide layer gets cracked and spalled, which leads to appearance of a new silver surface intensifying further oxidation. At last, AgO begins to form on the outer surface of the oxide film. The analytical results of the XPS and the AES attest to formation of a continuous high-quality protective oxide-based layer on the surface of ion-implanted silver films after exposure to AO. This layer can well protect materials in question from erosion.

  4. Templated green synthesis of plasmonic silver nanoparticles in onion epidermal cells suitable for surface-enhanced Raman and hyper-Raman scattering.

    Science.gov (United States)

    Espina Palanco, Marta; Bo Mogensen, Klaus; Gühlke, Marina; Heiner, Zsuzsanna; Kneipp, Janina; Kneipp, Katrin

    2016-01-01

    We report fast and simple green synthesis of plasmonic silver nanoparticles in the epidermal cells of onions after incubation with AgNO3 solution. The biological environment supports the generation of silver nanostructures in two ways. The plant tissue delivers reducing chemicals for the initial formation of small silver clusters and their following conversion to plasmonic particles. Additionally, the natural morphological structures of the onion layers, in particular the extracellular matrix provides a biological template for the growth of plasmonic nanostructures. This is indicated by red glowing images of extracellular spaces in dark field microscopy of onion layers a few hours after AgNO3 exposure due to the formation of silver nanoparticles. Silver nanostructures generated in the extracellular space of onion layers and within the epidermal cell walls can serve as enhancing plasmonic structures for one- and two-photon-excited spectroscopy such as surface enhanced Raman scattering (SERS) and surface enhanced hyper-Raman scattering (SEHRS). Our studies demonstrate a templated green preparation of enhancing plasmonic nanoparticles and suggest a new route to deliver silver nanoparticles as basic building blocks of plasmonic nanosensors to plants by the uptake of solutions of metal salts. PMID:27547600

  5. Propagation of plasmons in designed single crystalline silver nanostructures

    DEFF Research Database (Denmark)

    Kumar, Shailesh; Lu, Ying-Wei; Huck, Alexander;

    2012-01-01

    We demonstrate propagation of plasmons in single crystalline silver nanostructures fabricated using a combination of a bottom-up and a top-down approach. Silver nanoplates of thickness around 65 nm and a surface area of about 100 μm2 are made using a wet chemical method. Silver nanotips and nanow...

  6. A New Silver Complex with Ofloxacin – Preliminary Study

    Directory of Open Access Journals (Sweden)

    Rusu Aura

    2016-06-01

    Full Text Available Objective: Silver complexes of antibacterial quinolones have the potential advantage of combining the antibacterial activity of silver and fluoroquinolones. The objective of our study was the preparation and the preliminary physico-chemical characterization of a silver complex with ofloxacin.

  7. Autocatalytic Patterning with Silver Using Tin(II) Chloride Sensitizer

    Science.gov (United States)

    Mbindyo, Jeremiah K. N.; Anna, Laura J.; Fell, B. Andrew; Patton, David A.

    2011-01-01

    A silver mirror can be deposited on many types of surfaces from the reduction of the silver-diammine complex by a reducing sugar as proposed by Kemp in this "Journal". Three extensions of Kemp's demonstration that highlight the role of SnCl[subscript 2] sensitizer in the deposition of a silver mirror on surfaces are presented. The demonstration…

  8. Silver-functionalized carbon nanofiber composite electrodes for ibuprofen detection

    NARCIS (Netherlands)

    Manea, F.; Motoc, S.; Pop, A.; Remes, A.; Schoonman, J.

    2012-01-01

    The aim of this study is to prepare and characterize two types of silver-functionalized carbon nanofiber (CNF) composite electrodes, i.e., silver-decorated CNF-epoxy and silver-modified natural zeolite-CNF-epoxy composite electrodes suitable for ibuprofen detection in aqueous solution. Ag carbon nan

  9. Fabrication, characterization, and thermal property evaluation of silver nanofluids

    OpenAIRE

    Noroozi, Monir; Radiman, Shahidan; Zakaria, Azmi; Soltaninejad, Sepideh

    2014-01-01

    Silver nanoparticles were successfully prepared in two different solvents using a microwave heating technique, with various irradiation times. The silver nanoparticles were dispersed in polar liquids (distilled water and ethylene glycol) without any other reducing agent, in the presence of the stabilizer polyvinylpyrrolidone (PVP). The optical properties, thermal properties, and morphology of the synthesized silver particles were characterized using ultraviolet-visible spectroscopy, photopyro...

  10. Complex Macromolecular Architectures by Living Cationic Polymerization

    KAUST Repository

    Alghamdi, Reem D.

    2015-05-01

    Poly (vinyl ether)-based graft polymers have been synthesized by the combination of living cationic polymerization of vinyl ethers with other living or controlled/ living polymerization techniques (anionic and ATRP). The process involves the synthesis of well-defined homopolymers (PnBVE) and co/terpolymers [PnBVE-b-PCEVE-b-PSiDEGVE (ABC type) and PSiDEGVE-b-PnBVE-b-PSiDEGVE (CAC type)] by sequential living cationic polymerization of n-butyl vinyl ether (nBVE), 2-chloroethyl vinyl ether (CEVE) and tert-butyldimethylsilyl ethylene glycol vinyl ether (SiDEGVE), using mono-functional {[n-butoxyethyl acetate (nBEA)], [1-(2-chloroethoxy) ethyl acetate (CEEA)], [1-(2-(2-(t-butyldimethylsilyloxy)ethoxy) ethoxy) ethyl acetate (SiDEGEA)]} or di-functional [1,4-cyclohexanedimethanol di(1-ethyl acetate) (cHMDEA), (VEMOA)] initiators. The living cationic polymerizations of those monomers were conducted in hexane at -20 0C using Et3Al2Cl3 (catalyst) in the presence of 1 M AcOEt base.[1] The PCEVE segments of the synthesized block terpolymers were then used to react with living macroanions (PS-DPE-Li; poly styrene diphenyl ethylene lithium) to afford graft polymers. The quantitative desilylation of PSiDEGVE segments by n-Bu4N+F- in THF at 0 °C led to graft co- and terpolymers in which the polyalcohol is the outer block. These co-/terpolymers were subsequently subjected to “grafting-from” reactions by atom transfer radical polymerization (ATRP) of styrene to afford more complex macromolecular architectures. The base assisted living cationic polymerization of vinyl ethers were also used to synthesize well-defined α-hydroxyl polyvinylether (PnBVE-OH). The resulting polymers were then modified into an ATRP macro-initiator for the synthesis of well-defined block copolymers (PnBVE-b-PS). Bifunctional PnBVE with terminal malonate groups was also synthesized and used as a precursor for more complex architectures such as H-shaped block copolymer by “grafting-from” or

  11. Aggregate Formed by a Cationic Fluorescence Probe

    Institute of Scientific and Technical Information of China (English)

    TIAN, Juan; SANG, Da-Yong; JI, Guo-Zhen

    2007-01-01

    The aggregation behavior of a cationic fluorescence probe 10-(4,7,10,13,16-pentaoxa-1-azacyclooctadecyl-methyl)anthracen-9-ylmethyl dodecanoate (1) was observed and studied by a fluorescence methodology in acidic and neutral conditions. By using the Py scale, differences between simple aggregates and micelles have been discussed. The stability of simple aggregates was discussed in terms of hydrophobic interaction and electrostatic repulsion. The absence of excimer emission of the anthrancene moiety of probe 1 in neutral condition was attributed to the photoinduced electron transfer mechanism instead of photodimerization.

  12. Nanosecond laser ablation of silver nanoparticle film

    Science.gov (United States)

    Chung, Jaewon; Han, Sewoon; Lee, Daeho; Ahn, Sanghoon; Grigoropoulos, Costas P.; Moon, Jooho; Ko, Seung H.

    2013-02-01

    Nanosecond laser ablation of polyvinylpyrrolidone (PVP) protected silver nanoparticle (20 nm diameter) film is studied using a frequency doubled Nd:YAG nanosecond laser (532 nm wavelength, 6 ns full width half maximum pulse width). In the sintered silver nanoparticle film, absorbed light energy conducts well through the sintered porous structure, resulting in ablation craters of a porous dome shape or crown shape depending on the irradiation fluence due to the sudden vaporization of the PVP. In the unsintered silver nanoparticle film, the ablation crater with a clean edge profile is formed and many coalesced nanoparticles of 50 to 100 nm in size are observed inside the ablation crater. These results and an order of magnitude analysis indicate that the absorbed thermal energy is confined within the nanoparticles, causing melting of nanoparticles and their coalescence to larger agglomerates, which are removed following melting and subsequent partial vaporization.

  13. Roasting of refractory gold and silver concentrate

    International Nuclear Information System (INIS)

    In processing of precious metal ores with high pyrite content, refractory concentrates are obtained, which are difficult to process. A refractory gold and silver concentrate was leached with sodium cyanide. Results show low extraction percentages, being 34 % of gold and 40 % of silver. A roasting method to oxidize the concentrate was used, making it more susceptible to cyanidation, hence a more efficient way to extract precious metals. The variables include roasting temperature and roasting and cyanidation time. In addition, the hot calcine was added to the leaching solution at room temperature to analyze the effect on particle size and recovery. The best results, although not entirely satisfactory (50 % of gold and 61 % of silver) were obtained by roasting the concentrate for 4 h at 600 degree centigrade, followed by cyanidation for 20 h. The lime consumption to raise the pH to about 11.3 was increased markedly to 25 kg/m3. (Author) 11 refs.

  14. Silver nanoparticle containing silk fibroin bionanotextiles

    Energy Technology Data Exchange (ETDEWEB)

    Calamak, Semih; Aksoy, Eda Ayse [Hacettepe University, Department of Basic Pharmaceutical Sciences, Faculty of Pharmacy (Turkey); Erdogdu, Ceren; Sagıroglu, Meral [Hacettepe University, Department of Pharmaceutical Microbiology, Faculty of Pharmacy (Turkey); Ulubayram, Kezban, E-mail: ukezban@hacettepe.edu.tr [Hacettepe University, Department of Basic Pharmaceutical Sciences, Faculty of Pharmacy (Turkey)

    2015-02-15

    Development of new generation bionanotextiles is an important growing field, and they have found applications as wound dressings, bandages, tissue scaffolds, etc. In this study, silver nanoparticle (AgNP) containing silk-based bionanotextiles were fabricated by electrospinning, and processing parameters were optimized and discussed in detail. AgNPs were in situ synthesized within fibroin nanofibers by UV reduction of silver ions to metallic silver. The influence of post-treatments via methanol treatment and glutaraldehyde (GA) vapor exhibited changes in the secondary structure of silk. Methanol treatment increased the tensile properties of fibers due to supported crystalline silk structure, while GA vapor promoted amorphous secondary structure. AgNP containing silk fibroin bionanotextiles had strong antibacterial activity against gram-positive Staphylococcus aureus and gram-negative Pseudomonas aeruginosa.

  15. Silver nanoparticle containing silk fibroin bionanotextiles

    International Nuclear Information System (INIS)

    Development of new generation bionanotextiles is an important growing field, and they have found applications as wound dressings, bandages, tissue scaffolds, etc. In this study, silver nanoparticle (AgNP) containing silk-based bionanotextiles were fabricated by electrospinning, and processing parameters were optimized and discussed in detail. AgNPs were in situ synthesized within fibroin nanofibers by UV reduction of silver ions to metallic silver. The influence of post-treatments via methanol treatment and glutaraldehyde (GA) vapor exhibited changes in the secondary structure of silk. Methanol treatment increased the tensile properties of fibers due to supported crystalline silk structure, while GA vapor promoted amorphous secondary structure. AgNP containing silk fibroin bionanotextiles had strong antibacterial activity against gram-positive Staphylococcus aureus and gram-negative Pseudomonas aeruginosa

  16. Graded cluster algebras

    OpenAIRE

    Grabowski, Jan

    2015-01-01

    In the cluster algebra literature, the notion of a graded cluster algebra has been implicit since the origin of the subject. In this work, we wish to bring this aspect of cluster algebra theory to the foreground and promote its study. We transfer a definition of Gekhtman, Shapiro and Vainshtein to the algebraic setting, yielding the notion of a multi-graded cluster algebra. We then study gradings for finite type cluster algebras without coefficients, giving a full classification. Translating ...

  17. Nanostructural Features of Silver Nanoparticles Powder Synthesized through Concurrent Formation of the Nanosized Particles of Both Starch and Silver

    OpenAIRE

    A. Hebeish; El-Rafie, M. H.; El-Sheikh, M. A.; Mehrez E. El-Naggar

    2013-01-01

    Green innovative strategy was developed to accomplish silver nanoparticles formation of starch-silver nanoparticles (St-AgNPs) in the powder form. Thus, St-AgNPs were synthesized through concurrent formation of the nanosized particles of both starch and silver. The alkali dissolved starch acts as reducing agent for silver ions and as stabilizing agent for the formed AgNPs. The chemical reduction process occurred in water bath under high-speed homogenizer. After completion of the reaction, the...

  18. In-Situ Silver Acetylide Silver Nitrate Explosive Deposition Measurements Using X-Ray Fluorescence.

    Energy Technology Data Exchange (ETDEWEB)

    Covert, Timothy T.

    2014-09-01

    The Light Initiated High Explosive facility utilized a spray deposited coating of silver acetylide - silver nitrate explosive to impart a mechanical shock into targets of interest. A diagnostic was required to measure the explosive deposition in - situ. An X - ray fluorescence spectrometer was deployed at the facility. A measurement methodology was developed to measure the explosive quantity with sufficient accuracy. Through the use of a tin reference material under the silver based explosive, a field calibration relationship has been developed with a standard deviation of 3.2 % . The effect of the inserted tin material into the experiment configuration has been explored.

  19. Toward site-specific, homogeneous and highly stable fluorescent silver nanoclusters fabrication on triplex DNA scaffolds

    OpenAIRE

    Feng, Lingyan; Huang, Zhenzhen; Ren, Jinsong; Qu, Xiaogang

    2012-01-01

    A new strategy to create site-specific, homogeneous, and bright silver nanoclusters (AgNCs) with high-stability was demonstrated by triplex DNA as template. By reasonable design of DNA sequence, homogeneous Ag2 cluster was obtained in the predefined position of CG.C+ site of triplex DNA. This strategy was also explored for controlled alignment of AgNCs on the DNA nanoscaffold. To the best of our knowledge, this was the first example to simultaneously answer the challenges of excellent site-sp...

  20. catena-Poly[[tetra­kis­(hexa­methyl­phospho­ramide-κO)bis­(nitrato-κ2 O,O′)lutetium(III)] [silver(I)-di-μ-sulfido-tungstate(VI)-di-μ-sulfido

    OpenAIRE

    Jinfang Zhang

    2012-01-01

    In the title compound, {[Lu(NO3)2(C6H18N3OP)4][AgWS4]}n, hexamethylphosphoramide (hmp), tetrathiotungstate, silver iodide and lutetium nitrate were self-assembled, forming an anionic {[AgWS4]−}n chain extending parallel to [001]. The LuIII atom in the cation is coordinated by eight O atoms from two nitrate groups and four hmp ligands in a distorted square-antiprismatic geometry. Together with the two nitrate groups, the cation is monovalent, which leads to the anionic chain having a...

  1. Electronic spectra of oxygen containing polycyclic hydrocarbon cations and the protonated analogues

    Science.gov (United States)

    Chakraborty, Arghya; Fulara, Jan; Maier, John P.

    2015-08-01

    The electronic transitions of 9-fluorenone FL+ and 2,3,6,7-dibenzotropone DBT+ cations were detected in 6 K neon matrices following a mass-selective deposition. The absorptions at 649.2 and 472.2 nm are assigned to the 2 2 B 1 ← X ˜ 2 A 2 FL + and 2 2 A ' ← X ˜ 2 A ' DBT + transitions. Absorption spectra of protonated 9-fluorenone H+-FL and 2,3,6,7-dibenzotropone H+-DBT have also been measured. Protonation of the oxygenated polycyclic aromatic hydrocarbons is carried out in a hot cathode source via in situ produced protonated ethanol. Vibrationally resolved absorptions commencing at 423.3 nm of H-FL+ and two band systems of H-DBT+ with origins at 502.4 and 371.5 nm are assigned to the 2 1 A ' ← X ˜ 1 A ' electronic transition of 9-hydroxy-fluorenyl cation and 1 1 A ← X ˜ 1 A , 2 1 A ← X ˜ 1 A of 2,3,6,7-dibenzocycloheptenol cation. The assignments are based on vertical excitation energy calculations with time dependent density functional theory, symmetry adapted cluster configuration interaction, and MS-CASPT2 methods.

  2. Manufacturing of superconductive silver/ceramic composites

    DEFF Research Database (Denmark)

    Seifi, Behrouz; Bech, Jakob Ilsted; Eriksen, Morten;

    2000-01-01

    Manufacturing of superconducting metal/ceramic composites is a rather new discipline within materials forming processes. High Temperature SuperConductors, HTSC, are manufactured applying the Oxide-Powder-In-Tube process, OPIT. A ceramic powder containing lead, calcium, bismuth, strontium......, and copper oxides is inserted into a silver tube and reduced by multi-step drawing. These single-filaments are packed in a new silver tube thus forming a multi-filament containing e.g. 37 single-filaments, which is subsequently reduced by drawing and rolling to tapes approximately 0.2 mm thick by 3 mm wide...

  3. Fluorescent DNA Stabilized Silver Nanoclusters as Biosensors

    Directory of Open Access Journals (Sweden)

    Alfonso Latorre

    2013-01-01

    Full Text Available DNA stabilized fluorescent silver nanoclusters are promising materials, of which fluorescent properties can be exploited to develop sensors. Particularly, the presence of a DNA strand in the structure has promoted the development of gene sensors where one part of the sensor is able to recognize the target gene sequence. Moreover, since oligonucleotides can be designed to have binding properties (aptamers a variety of sensors for proteins and cells have been developed using silver nanoclusters. In this review the applications of this material as sensors of different biomolecules are summarized.

  4. Recovery of silver from CEPOD anolyte solutions

    International Nuclear Information System (INIS)

    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 PuO2 (and other Pu species) to (PuO2)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 CO2 or H2O, 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 (C6H8O6) 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

  5. Gold and Silver Inlaid Bronze Sheep

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Gold and silver inlaying is a metal processing technique popular during the Spring and Autumn Period (770-476 B. C.) and the Warring States Period (475-221 B. C.). Patterns on the surface of the bronze figure are chiselled out and gold and silver threads (which can be as thin as hair) are inlaid. Finally the whole figure is filed and polished resulting in a splendid artistic work highlighting the different colours of the three different kinds of metal. The artifact shown here was unearthed from Ningxia'...

  6. Mineral resource of the month: silver

    Science.gov (United States)

    Katrivanos, Florence C.

    2015-01-01

    Silver, one of the eight precious or noble metals, has been used extensively throughout recorded history for various medical purposes, ornaments and utensils, and for its intrinsic value as the basis for trade and monetary systems. Silver has played a significant role in world history, financing a Greek victory over the Persians in 480 B.C., helping Spain become a world power in the 16th and 17th centuries, and helping fund the Union forces during the U.S. Civil War, to give a few examples.

  7. Cationic Antimicrobial Polymers and Their Assemblies

    Directory of Open Access Journals (Sweden)

    Ana Maria Carmona-Ribeiro

    2013-05-01

    Full Text Available Cationic compounds are promising candidates for development of antimicrobial agents. Positive charges attached to surfaces, particles, polymers, peptides or bilayers have been used as antimicrobial agents by themselves or in sophisticated formulations. The main positively charged moieties in these natural or synthetic structures are quaternary ammonium groups, resulting in quaternary ammonium compounds (QACs. The advantage of amphiphilic cationic polymers when compared to small amphiphilic molecules is their enhanced microbicidal activity. Besides, many of these polymeric structures also show low toxicity to human cells; a major requirement for biomedical applications. Determination of the specific elements in polymers, which affect their antimicrobial activity, has been previously difficult due to broad molecular weight distributions and random sequences characteristic of radical polymerization. With the advances in polymerization control, selection of well defined polymers and structures are allowing greater insight into their structure-antimicrobial activity relationship. On the other hand, antimicrobial polymers grafted or self-assembled to inert or non inert vehicles can yield hybrid antimicrobial nanostructures or films, which can act as antimicrobials by themselves or deliver bioactive molecules for a variety of applications, such as wound dressing, photodynamic antimicrobial therapy, food packing and preservation and antifouling applications.

  8. Cobalt 60 cation exchange with mexican clays

    International Nuclear Information System (INIS)

    Mexican clays can be used to remove radioactive elements from contaminated aqueous solutions. Cation exchange experiments were performed with 60 Co radioactive solution. In the present work the effect of contact time on the sorption of Co 2+ was studied. The contact time in hydrated montmorillonite was from 5 to 120 minutes and in dehydrated montmorillonite 5 to 1400 minutes. The Co 2+ uptake value was, in hydrated montmorillonite, between 0.3 to 0.85 m eq/g and in dehydrated montmorillonite, between 0.6 to 1.40 m eq/g. The experiments were done in a pH 5.1 to 5.7 and normal conditions. XRD patterns were used to characterize the samples. The crystallinity was determined by X-ray Diffraction and it was maintained before and after the cation exchange. DTA thermo grams showed the temperatures of the lost humidity and crystallization water. Finally, was observed that dehydrated montmorillonite adsorb more cobalt than hydrated montmorillonite. (Author)

  9. Cluster size matters: Size-driven performance of subnanometer clusters in catalysis, electrocatalysis and Li-air batteries

    Science.gov (United States)

    Vajda, Stefan

    2015-03-01

    This paper discusses the strongly size-dependent performance of subnanometer cluster based catalysts in 1) heterogeneous catalysis, 2) electrocatalysis and 3) Li-air batteries. The experimental studies are based on I. fabrication of ultrasmall clusters with atomic precision control of particle size and their deposition on oxide and carbon based supports; II. test of performance, III. in situand ex situ X-ray characterization of cluster size, shape and oxidation state; and IV.electron microscopies. Heterogeneous catalysis. The pronounced effect of cluster size and support on the performance of the catalyst (catalyst activity and the yield of Cn products) will be illustrated on the example of nickel and cobalt clusters in Fischer-Tropsch reaction. Electrocatalysis. The study of the oxygen evolution reaction (OER) on size-selected palladium clusters supported on ultrananocrystalline diamond show pronounced size effects. While Pd4 clusters show no reaction, Pd6 and Pd17 clusters are among the most active catalysts known (in in terms of turnover rate per Pd atom). The system (soft-landed Pd4, Pd6, or Pd17 clusters on an UNCD Si coated electrode) shows stable electrochemical potentials over several cycles, and the characterization of the electrodes show no evidence for evolution or dissolution of either the support Theoretical calculations suggest that this striking difference may be a demonstration that bridging Pd-Pd sites, which are only present in three-dimensional clusters, are active for the oxygen evolution reaction in Pd6O6. Li-air batteries. The studies show that sub-nm silver clusters have dramatic size-dependent effect on the lowering of the overpotential, charge capacity, morphology of the discharge products, as well as on the morphology of the nm size building blocks of the discharge products. The results suggest that by precise control of the active surface sites on the cathode, the performance of Li-air cells can be significantly improved

  10. Influence of interlayer cations on organic intercalation of montmorillonite.

    Science.gov (United States)

    Wu, Limei; Liao, Libing; Lv, Guocheng

    2015-09-15

    The influence of the types of interlayer cations on organic intercalation of montmorillonite (Mt) was studied in this paper. The distribution of Na(+), K(+), Mg(2+), Ca(2+) and Fe(3+) in montmorillonite interlayer, their interaction with structure layers and the effect of interlayer cations on the basal spacing of Mt, the amount of binding water for different interlayer cations and the binding force between them were investigated systematically. 1-Hexadecy1-3-methylimidazolium chloride monohydrate (C16mimCl) was intercalated into montmorillonites with different interlayer cations. The influence of interlayer cations on organic intercalation was investigated. Molecular dynamics (MD) modeling was used to speculate the interlayer microstructures of the organically intercalated Mt with different interlayer cations. These simulations help to predict the microstructure of organo-Mt and guide their relevant engineering applications. PMID:26001131

  11. Monodisperse Silver Nanoparticles Synthesized by a Microwave-Assisted Method

    Institute of Scientific and Technical Information of China (English)

    ZHU Shao-Peng; TANG Shao-Chun; MENG Xiang-Kang

    2009-01-01

    Silver nanoparticles with an average size of about 2Onto are synthesized in a colloidal solution with the aid of microwave irradiation. Neither additional reductant nor stabilizer is required in this microwave-assisted method.The color of the colloidal solution is found to be dark green, different from the characteristic yellow of silver colloidal solutions. The silver nanoparticles in the colloidal solution have a narrow size distribution and large yield quantity. UV-visible absorption spectroscopy analysis reveals that the as-synthesized monodisperse silver nanoparticles have exceptional optical properties. Raman spectroscopy measurements demonstrate that these silver nanoparticles exhibit a notable surface-enhanced Raman scattering ability.

  12. Interdisciplinary Research to Elucidate Mechanisms Governing Silver Nanoparticle Fate and Transport in Porous Media

    Science.gov (United States)

    Pennell, K. D.; Mittleman, A.; Taghavy, A.; Fortner, J.; Lantagne, D.; Abriola, L. M.

    2015-12-01

    Interdisciplinary Research to Elucidate Mechanisms Governing Silver Nanoparticle Fate and Transport in Porous Media Anjuliee M. Mittelman, Amir Taghavy, Yonggang Wang, John D. Fortner, Daniele S. Lantagne, Linda M. Abriola and Kurt D. Pennell* Detailed knowledge of the processes governing nanoparticle transport and reactivity in porous media is essential for accurate predictions of environmental fate, water and wastewater treatment system performance, and assessment of potential risks to ecosystems and water supplies. To address these issues, an interdisciplinary research team combined experimental and mathematical modeling studies to investigate the mobility, dissolution, and aging of silver nanoparticles (nAg) in representative aquifer materials and ceramic filters. Results of one-dimensional column studies, conducted with water-saturated sands maintained at pH 4 or 7 and three levels of dissolved oxygen (DO), revealed that fraction of silver mass eluted as Ag+ increased with increasing DO level, and that the dissolution of attached nAg decreased over time as a result of surface oxidation. A hybrid Eulerain-Lagragian nanoparticle transport model, which incorporates DO-dependent dissolution kinetics and particle aging, was able to accurately simulate nAg mobility and Ag+ release measured in the column experiments. Model sensitivity analysis indicated that as the flow velocity and particle size decrease, nAg dissolution and Ag+ transport processes increasingly govern silver mobility. Consistent results were obtained in studies of ceramic water filters treated with nAg, where silver elution was shown to be governed by nAg dissolution to form Ag+ and subsequent cation exchange reactions. Recent studies explored the effects of surface coating aging on nAg aggregation, mobility and dissolution. Following ultraviolet light, nAg retention in water saturated sand increased by 25-50%, while up to 50% of the applied mass eluted as Ag+ compared to less than 1% for un-aged n

  13. Interdisciplinary Research to Elucidate Mechanisms Governing Silver Nanoparticle Fate and Transport in Porous Media

    Science.gov (United States)

    Pennell, K. D.; Mittleman, A.; Taghavy, A.; Fortner, J.; Lantagne, D.; Abriola, L. M.

    2014-12-01

    Interdisciplinary Research to Elucidate Mechanisms Governing Silver Nanoparticle Fate and Transport in Porous Media Anjuliee M. Mittelman, Amir Taghavy, Yonggang Wang, John D. Fortner, Daniele S. Lantagne, Linda M. Abriola and Kurt D. Pennell* Detailed knowledge of the processes governing nanoparticle transport and reactivity in porous media is essential for accurate predictions of environmental fate, water and wastewater treatment system performance, and assessment of potential risks to ecosystems and water supplies. To address these issues, an interdisciplinary research team combined experimental and mathematical modeling studies to investigate the mobility, dissolution, and aging of silver nanoparticles (nAg) in representative aquifer materials and ceramic filters. Results of one-dimensional column studies, conducted with water-saturated sands maintained at pH 4 or 7 and three levels of dissolved oxygen (DO), revealed that fraction of silver mass eluted as Ag+ increased with increasing DO level, and that the dissolution of attached nAg decreased over time as a result of surface oxidation. A hybrid Eulerain-Lagragian nanoparticle transport model, which incorporates DO-dependent dissolution kinetics and particle aging, was able to accurately simulate nAg mobility and Ag+ release measured in the column experiments. Model sensitivity analysis indicated that as the flow velocity and particle size decrease, nAg dissolution and Ag+ transport processes increasingly govern silver mobility. Consistent results were obtained in studies of ceramic water filters treated with nAg, where silver elution was shown to be governed by nAg dissolution to form Ag+ and subsequent cation exchange reactions. Recent studies explored the effects of surface coating aging on nAg aggregation, mobility and dissolution. Following ultraviolet light, nAg retention in water saturated sand increased by 25-50%, while up to 50% of the applied mass eluted as Ag+ compared to less than 1% for un-aged n

  14. The application of Guided Ion Beam Tandem Mass Spectrometer; Bond dissociation energies of bare and ligated copper group cluster anions

    International Nuclear Information System (INIS)

    Threshold energies, fragmentation patterns, and integral cross sections for the reactions of collision induced dissociations of bare and ligated copper group cluster anions are determined using a Guided Ion Beam Tandem Mass Spectrometer (GIB-MS). The bond breaking patterns for the copper cluster anions show dramatic even/odd tendencies, e.g., all copper group anions generate as the predominant reaction product, Carbon monoxide is weakly bound to copper group cluster anions. Cohesive energies of the bare copper and silver cluster anions are determined and exhibit a good correspondence with estimate cohesive energies by the model of Miedema.

  15. PVDF nanofibers with silver nanoparticles and silver/titanium dioxide for antimicrobial applications

    International Nuclear Information System (INIS)

    PVDF nanofibers with and without nanoparticles were produced by the method of electro spinning using dimethylformamide (DMF). Silver nitrate nanoparticles (0,5 and 2 wt %) and silver/titanium dioxide nanoparticles obtained by the reduction method (2 wt %) were synthesized and added to the PVDF solution to prepared nanofibers. The processes of electrospinning and film preparation using PVDF with the nanoparticles were compared. Silver/titanium dioxide nanoparticles were characterized with X-ray diffraction (XRD), Scanning electron microscopy (SEM) with EDX and x-ray photoelectron spectroscopy (XPS) to show silver/titanium dioxide nanoparticles. Nanofibers mats were characterized with SEM to study the effects of the addition of the nanoparticles on the morphology behavior and spectroscopy by Fourier transform infrared (FTIR) to analyze the crystalline phase of PVDF films. (author)

  16. Determination of the silver content of ancient silver coins by neutron activation analysis

    International Nuclear Information System (INIS)

    A reactor neutron activation analysis procedure for the determination of the silver content of silver coins is described. The samples are irradiated for 1 s, cooled for 85 s and measured for 60 s with a Ge-detector. The analysis is based on the measurement of sup(110)Ag and sup(108)Ag. Aluminium is used for flux monitoring and pulse pile-up correction. A calibration curve is prepared by irradiating and measuring a series of discs with known silver contents. An average precision of +-2.1% is obtained. The analysis of coins with known silver contents shows good agreement with the given values. The analysis time is 2.5 minutes per sample. (author)

  17. Photosensitized synthesis of silver nanoparticles using Withania somnifera leaf powder and silver nitrate.

    Science.gov (United States)

    Raut, Rajesh Warluji; Mendhulkar, Vijay Damodhar; Kashid, Sahebrao Balaso

    2014-03-01

    The metal nanoparticle synthesis is highly explored field of nanotechnology. The biological methods seem to be more effective; however, due to slow reduction rate and polydispersity of the resulting products, they are less preferred. In the present study, we report rapid and facile synthesis of silver nanoparticles at room temperature. The exposure of reaction mixtures containing silver nitrate and dried leaf powder of Withania somnifera Linn to direct sunlight resulted in reduction of metal ions within five minutes whereas, the dark exposure took almost 12h. Further studies using different light filters reveal the role of blue light in reduction of silver ions. The synthesized silver nanoparticles were characterized by UV-Vis, Infrared spectroscopy (IR), Transmission Electron Microscopy (TEM), X-ray Diffraction studies (XRD), Nanoparticle Tracking Analysis (NTA), Energy Dispersive Spectroscopy (EDS), and Cyclic Voltammetry (CV). The Antibacterial and antifungal studies showed significant activity as compared to their respective standards.

  18. Bespoke cationic nano-objects via RAFT aqueous dispersion polymerisation

    OpenAIRE

    Williams, M.; Penfold, NJW; Lovett, JR; Warren, NJ; Douglas, CWI; Doroshenko, N; Verstraete, P; Smets, J; Armes, SP

    2016-01-01

    A range of cationic diblock copolymer nanoparticles are synthesised via polymerisation-induced self-assembly (PISA) using a RAFT aqueous dispersion polymerisation formulation. The cationic character of these nanoparticles can be systematically varied by utilising a binary mixture of two macro-CTAs, namely non-ionic poly(glycerol monomethacrylate) (PGMA) and cationic poly[2-(methacryloyloxy)ethyl]trimethylammonium chloride (PQDMA), with poly(2-hydroxypropyl methacrylate) (PHPMA) being selected...

  19. Development of Recombinant Cationic Polymers for Gene Therapy Research

    OpenAIRE

    Canine, Brenda F.; Hatefi, Arash

    2010-01-01

    Cationic polymers created through recombinant DNA technology have the potential to fill a void in the area of gene delivery. The recombinant cationic polymers to be discussed here are amino acid based polymers synthesized in E.coli with the purpose to not only address the major barriers to efficient gene delivery but offer safety, biodegradability, targetability and cost-effectiveness. This review helps the readers to get a better understanding about the evolution of recombinant cationic poly...

  20. Development of Antibiotics Impregnated Nanosized Silver Phosphate-Doped Hydroxyapatite Bone Graft

    Directory of Open Access Journals (Sweden)

    Waraporn Suvannapruk

    2013-01-01

    Full Text Available Nanosized Ag3PO4 loaded hydroxyapatite which was prepared by a novel low temperature phosphorization of 3D printed calcium sulfate dihydrate at the nominal silver concentration of 0.001 M and 0.005 M was impregnated by two antibiotics including gentamicin and vancomycin. Phase composition, microstructure, antibiotics loading, silver content, antimicrobial performance, and cytotoxic potential of the prepared samples were characterized. It was found that the fabricated sample consisted of hydroxyapatite as a main phase and spherical-shaped silver phosphate nanoparticles distributing within the cluster of hydroxyapatite crystals. Antibacterial activity of the samples against two bacterial strains (gram negative P. aeruginosa and gram positive S. aureus was carried out. It was found that the combination of antibiotics and nanosized Ag3PO4 in hydroxyapatite could enhance the antibacterial performance of the samples by increasing the duration in which the materials exhibited antibacterial property and the size of the inhibition zone depending on the type of antibiotics and bacterial strains compared to those contained antibiotics or nanosilver phosphate alone. Cytotoxic potential against osteoblasts of antibiotics impregnated nanosilver phosphate hydroxyapatite was found to depend on the combination of antibiotics content, type of antibiotics, and nanosilver phosphate content.

  1. Process variables in biomimetic synthesis of silver nanoparticles by aqueous extract of Azadirachta indica (Neem) leaves

    Energy Technology Data Exchange (ETDEWEB)

    Tripathy, A. [VIT University, School of Biotechnology, Chemical and Biomedical Engineering (India); Raichur, Ashok M. [Indian Institute of Science, Department of Materials Engineering (India); Chandrasekaran, N.; Prathna, T. C.; Mukherjee, Amitava, E-mail: amit.mookerjea@gmail.co [VIT University, School of Biotechnology, Chemical and Biomedical Engineering (India)

    2010-01-15

    Owing to widespread applications, synthesis and characterization of silver nanoparticles is recently attracting considerable attention. Increasing environmental concerns over chemical synthesis routes have resulted in attempts to develop biomimetic approaches. One of them is synthesis using plant parts, which eliminates the elaborate process of maintaining the microbial culture and often found to be kinetically favourable than other bioprocesses. The present study deals with investigating the effect of process variables like reductant concentrations, reaction pH, mixing ratio of the reactants and interaction time on the morphology and size of silver nanoparticles synthesized using aqueous extract of Azadirachta indica (Neem) leaves. The formation of crystalline silver nanoparticles was confirmed using X-ray diffraction analysis. By means of UV spectroscopy, Scanning and Transmission Electron Microscopy techniques, it was observed that the morphology and size of the nanoparticles were strongly dependent on the process parameters. Within 4 h interaction period, nanoparticles below 20-nm-size with nearly spherical shape were produced. On increasing interaction time (ageing) to 66 days, both aggregation and shape anisotropy (ellipsoidal, polyhedral and capsular) of the particles increased. In alkaline pH range, the stability of cluster distribution increased with a declined tendency for aggregation of the particles. It can be inferred from the study that fine tuning the bioprocess parameters will enhance possibilities of desired nano-product tailor made for particular applications.

  2. Interaction between silver and Zircaloy-4 at high temperatures

    International Nuclear Information System (INIS)

    Interaction between silver-indium-cadmium control rod alloy and Zircaloy-4 is an important reaction in the analysis of a severe accident of a PWR, since it has a great influence on the fuel bundle degradation. The authors have reported the results of the experiments on the interaction between silver-indium-cadmium alloy and Zircaloy-4. To examine the mechanism of this complex reaction system, reaction couples of silver, the main component of silver-indium-cadmium alloy, and Zircaloy-4 were isothermally heated in argon at the temperatures ranging from 1273 to 1473 K. The dissolution behavior of Zircaloy-4 in silver/Zircaloy-4 reaction was compared with that in silver-indium-cadmium alloy/Zircaloy-4 reaction and the role of indium was discussed. The reaction rate of silver/Zircaloy-4 reaction increased with the temperature increase and was low compared to that of silver-indium-cadmium alloy/Zircaloy-4 reaction. This difference is larger at lower test temperatures and is believed to be caused by the difference of melting points between silver-indium-cadmium alloy and silver. Two reactions show comparable reaction rate at 1473K. Silver/Zircaloy-4 reaction approximately obeyed the parabolic rate law, thereby reaction rate constants and an apparent activation energy, 580.8kJ/mol, were determined. (author)

  3. CdS clusters in pores of zeolite X

    International Nuclear Information System (INIS)

    The crystal structures of the hydrated and dehydrated forms of zeolites involving CdS clusters are determined by X-ray diffraction. Crystals with the CdS clusters obtained by repeated exchanges in a Na2S solution or treatment with H2S vapor are investigated. It is found that only the CdS molecules are located in the large cavities of the CdX(Na2S) crystals. The CdX(H2S) crystals contain the [Cd20S13]14+ clusters in the large cavities. It is shown that these clusters are built up around the S atoms, which are situated at the centers of the large cavities of zeolite and coordinated tetrahedrally by Cd atoms. These atoms are bound through sulfur atoms with Cd cations situated near the walls of the cavity in the environment of the aluminosilicate framework oxygens

  4. Metal-Enhanced Fluorescence of Silver Island Associated with Silver Nanoparticle

    OpenAIRE

    Liaw, Jiunn-Woei; Wu, Hsin-Yu; Huang, Chu-Chuan; Kuo, Mao-Kuen

    2016-01-01

    The coupling plasmon of a hybrid nanostructure, silver island (SI) associated with silver nanoparticle (SNP), on metal-enhanced fluorescence (MEF) was studied theoretically. We used the multiple multipole method to analyze the plasmon-mediated enhancement factor on the fluorescence of a molecule immobilized on SNP and located in the gap zone between SI and SNP; herein, the SI was modeled as an oblate spheroid. Numerical results show that the enhancement factor of the hybrid nanostructure is h...

  5. Structural and optical properties of Si-doped Ag clusters

    KAUST Repository

    Mokkath, Junais Habeeb

    2014-03-06

    The structural and optical properties of AgN and Ag N-1Si1 (neutral, cationic, and anionic) clusters (N = 5 to 12) are systematically investigated using the density functional based tight binding method and time-dependent density functional theory, providing insight into recent experiments. The gap between the highest occupied and lowest unoccupied molecular orbitals and therefore the optical spectrum vary significantly under Si doping, which enables flexible tuning of the chemical and optical properties of Ag clusters. © 2014 American Chemical Society.

  6. Study of the Electroless Silver Seed Formation on Silicon Surface

    Institute of Scientific and Technical Information of China (English)

    TONG Hao; WANG Chun-Ming; YE Wei-Chun; CHANG Yan-Long; LI Hu-Lin

    2007-01-01

    The silver seed on silicon was prepared through aqueous HF and AgNO3 solution at room temperature. In order to explore the formation process of silver seed on silicon, the methods of open circuit potential with time (OCP-t),anodic stripping sweep voltammetry (ASV) and scanning tunneling microscope (STM) were used in this work. The procedure of silver nucleus growing into large particles was explained by electro-negativity. The growth mechanism of silver seed on silicon has been presented: at first, the silver monolayer and multilayer firstly grows onto silicon without fully covering the surface at the expense of silicon etching due to the silver seed attracting the electron from silicon, after that, the monolayer coalesces together, forming continuous grain film with some silver atoms diffusing into the silicon and the multilayer still grows thick simultaneously.

  7. Evaluation of the antimicrobial efficacy of phytogenic silver nanoparticles

    Institute of Scientific and Technical Information of China (English)

    Prasad TNVKV; Elumalai EK; Khateeja S

    2011-01-01

    Objective: To evaluate the antimicrobial activity of silver nanoparticles synthesized fromPsidium guajava (P. guajava) against human pathogens. Methods: Ultraviolet-visible (UV-Vis) spectrophotometry and transmission electron microscopy (TEM) were performed to confirm the formation and stability of silver nanparticles. Antimicrobial activities of the synthesized Ag nanoparticles were determined using the agar well diffusion assay method. Results: UV-Vis spectrum of the aqueous medium containing silver nanoparticles showed absorption peak at around 410 nm. TEM showed the formation of silver nanoparticles with an average size of 59 nm. The formed silver nanoparticles showed good antimicrobial activity against Escherichia coli,Bacillus cereus and Candida tropicalis. Conclusions: P. guajava demonstrated strong potential for synthesis of silver nanoparticles by rapid reduction of silver ions (Ag+ to Ag0). Biological methods are a good competent for the chemical procedures, which are environment friendly and convenient.

  8. Synthesis and characterization of silver nanoparticles by sonoelectrodeposition

    Institute of Scientific and Technical Information of China (English)

    CHENG Jingquan; YAO Suwei

    2005-01-01

    Shaped silver nanoparticles with sphere, wire and dendrite were prepared by sonoelectrochemical deposition from an aqueous solution of AgNO3 in the presence of ethylenediaminetetraacetic acid disodium salt (EDTA) and polyvinylpyrrolidone (PVP). The diameter of spherical silver particles was about 30 nm. The diameter of the silver nanowires was also about 30 nm and the length was 200-900 nm. The dendrites were synthesized with the concentration of silver solution increasing. Silver nanoparticles were characterized by transmission electron microscope (TEM), X-ray powder diffraction (XRD), scanning probe microscope (SPM) and UV-vis absorption spectrum. XRD patterns revealed that silver particles were of face-centered cubic structure. UV-vis absorption spectra indicated that different morphology and size of silver particles could influence the optical properties.

  9. The molecular orientation of PNBA on silver nanoparticles

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    The molecular orientations of p-nitrobenzoic acid (PNBA) on the surface of silver nanoparticles and silver mirror have been investigated by using surface enhanced Raman scattering (SERS) and UV-visible absorption spectroscopy. In the mixed system of silver colloid/PNBA/ethanol, the orientation of PNBA on silver nanoparticles remarkably different from that on silver mirror was observed, and it mainly resulted from the cooperation effect of the adsorption to surface active sites on silver under the pressure of aqueous molecules. This result is of some significance for further studying surface-interfacial structures and properties of silver nanoparticles, and the technique used in this note is feasible to get the SERS spectra of some molecules insoluble in aqueous solution.

  10. Role of Silver-Nano Particles in Drug Discovery Research

    Directory of Open Access Journals (Sweden)

    Richa Khare

    2016-03-01

    Full Text Available is the only precious metal has been used to fight infection for thousands of years. Hippocrates first described its antimicrobial properties in 400 BC but how it works has been a mystery. It has a long history as an antibiotic in human health care and also used for many purposes. Silver compounds are very effective antibacterial agents against both aerobic and anaerobic bacteria. It has been developed for use in water purification, wound care, bone prostheses, reconstructive orthopaedic surgery, cardiac devices, catheters and surgical appliances. Advancing biotechnology has enabled incorporation of ionizable silver into fabrics for clinical use to reduce the risk of infections and for personal hygiene. The antimicrobial action of silver or silver compounds is proportional to the bioactive silver ion (Ag (+ released and its availability to interact with bacterial or fungal cell membranes. Silver metal and inorganic silver compounds ionize in the presence of water, body fluids or tissue exudates

  11. Synthesis of silver nanoparticles in melts of amphiphilic polyesters

    International Nuclear Information System (INIS)

    The current work presents a one-step procedure for the synthesis of amphiphilic silver nanoparticles suitable for production of silver-filled polymeric materials. This solvent free synthesis via reduction of Tollens’ reagent as silver precursor in melts of amphiphilic polyesters consisting of hydrophilic poly(ethylene glycol) blocks and hydrophobic alkyl chains allows the production of silver nanoparticles without any by-product formation. This makes them especially interesting for the production of medical devices with antimicrobial properties. In this article the influences of the chain length of the hydrophobic block in the amphiphilic polyesters and the process temperature on the particle size distribution (PSD) and the stability of the particles against agglomeration are discussed. According to the results of spectroscopic and viscosimetric investigations the silver precursor is reduced to elemental silver nanoparticles by a single electron transfer process from the poly(ethylene glycol) chain to the silver ion. (paper)

  12. Extracellular biosynthesis of silver nanoparticles using the fungus Fusarium semitectum

    International Nuclear Information System (INIS)

    Development of environmental friendly procedures for the synthesis of metal nanoparticles through biological processes is evolving into an important branch of nanobiotechnology. In this paper, we report on the use of fungus 'Fusarium semitectum' for the extracellular synthesis of silver nanoparticles from silver nitrate solution (i.e. through the reduction of Ag+ to Ag0). Highly stable and crystalline silver nanoparticles are produced in solution by treating the filtrate of the fungus F. semitectum with the aqueous silver nitrate solution. The formations of nanoparticles are understood from the UV-vis and X-ray diffraction studies. Transmission electron microscopy of the silver particles indicated that they ranged in size from 10 to 60 nm and are mostly spherical in shape. Interestingly the colloidal suspensions of silver nanoparticles are stable for many weeks. Possible medicinal applications of these silver nanoparticles are envisaged

  13. What Makes Clusters Decline?

    DEFF Research Database (Denmark)

    Østergaard, Christian Richter; Park, Eun Kyung

    2015-01-01

    Most studies on regional clusters focus on identifying factors and processes that make clusters grow. However, sometimes technologies and market conditions suddenly shift, and clusters decline. This paper analyses the process of decline of the wireless communication cluster in Denmark....... The longitudinal study on the high-tech cluster reveals that technological lock-in and exit of key firms have contributed to decline. Entrepreneurship has a positive effect on the cluster’s adaptive capabilities, while multinational companies have contradicting effects by bringing in new resources to the cluster...

  14. Textural characterization of foxtail millet gels: effect of cations and hydrocolloids.

    Science.gov (United States)

    Nagaprabha, P; Bhattacharya, Sila

    2016-01-01

    Foxtail millet (Setaria italica) is traditionally cultivated in mainly dry land areas and has nutritional importance. The textural characteristics of gels, formed with foxtail millet flour at different concentrations (9-13 %, dry solid basis) along with selected cations and hydrocolloids, were determined. Different concentrations of monovalent (NaCl) and divalent (CaCl2 and FeSO4) cations, and hydrocolloids such as gelatin, gellan, starch, xanthan and agar were incorporated in gels. The gel forming ability markedly improved with an increase in the concentrations of CaCl2 and FeSO4, while NaCl had a marginal effect. Gels prepared with 11 % of foxtail millet alone were found to sensorially acceptable while addition of 0.5 % CaCl2 or 0.2 % FeSO4 respective with 10 % foxtail millet also resulted in acceptable gels. Among the hydrocolloids, starch and gellan had marked effects on gel formation, and textural and sensory attributes. The principal component analysis (PCA) plot showed that concentration of foxtail millet formed a cluster with sensory hardness, springiness, cohesiveness, and instrumental peak stress, fracture strain and compression energy indicating that these attributes were interrelated to each other. Stickiness and gelling time formed a cluster on the other side of the axis indicating inversely related. Foxtail millet has a good potential for development of new ranges of gelled health benefiting convenience products with nutraceutical property, and the addition of cations helps to achieve acceptable structural integrity. PMID:26787947

  15. Multiple surface plasmon polaritons modes on thin silver film controlled by a two-dimensional lattice of silver nanodimers

    Energy Technology Data Exchange (ETDEWEB)

    Chang, Ying; Jiang, Yongyuan, E-mail: jiangyy@hit.edu.cn [Harbin Institute of Technology, Department of Physics (China)

    2015-01-15

    We study the optical resonant spectrum of a two-dimensional periodic array of silver nanodimers on a thin silver film using multiple scattering formalism. The excited multiple plasmonic modes on two interfaces of the silver film reveal that the dispersion relationships of surface plasmon polaritons on metallic film are modified by doubly periodic lattice due to the fact that wave vectors matching conditions are satisfied. Moreover, we demonstrate that the plasmonic modes are directly controlled by the thickness of silver film, as well as the gap between nanodimer array and silver film. These effects provide novel high-efficient and steady way for excitation in future plasmonic nanodevices.

  16. Electrospun polyacrylonitrile nanofibers loaded with silver nanoparticles by silver mirror reaction.

    Science.gov (United States)

    Shi, Yongzheng; Li, Yajing; Zhang, Jianfeng; Yu, Zhongzhen; Yang, Dongzhi

    2015-06-01

    The silver mirror reaction (SMR) method was selected in this paper to modify electrospun polyacrylonitrile (PAN) nanofibers, and these nanofibers loaded with silver nanoparticles showed excellent antibacterial properties. PAN nanofibers were first pretreated in AgNO3 aqueous solution before the SMR process so that the silver nanoparticles were distributed evenly on the outer surface of the nanofibers. The final PAN nanofibers were characterized by scanning electron microscopy (SEM), energy dispersive spectrometer (EDS), transmission electron microscopy (TEM), TEM-selected area electron diffraction (SAED), X-ray diffraction (XRD) and thermogravimetric analysis (TGA). SEM, TEM micrographs and SAED patterns confirmed homogeneous dispersion of the silver nanoparticles which were composed of monocrystals with diameters 20-30nm. EDS and XRD results showed that these monocrystals tended to form face-centered cubic single silver. TGA test indicated that the nanoparticles loaded on the nanofibers reached above 50wt.%. This material was also evaluated by the viable cell-counting method. The results indicated that PAN nanofibers loaded with silver nanoparticles exhibited excellent antimicrobial activities against gram-negative Escherichia coli (E. coli), gram-positive Staphylococcus aureus (S. aureus) and the fungus Monilia albicans. Thus, this material had many potential applications in biomedical fields. PMID:25842144

  17. Reinforcement of Conducting Silver-based Materials

    Directory of Open Access Journals (Sweden)

    Heike JUNG

    2014-09-01

    Full Text Available Silver is a well-known material in the field of contact materials because of its high electrical and thermal conductivity. However, due to its bad mechanical and switching properties, silver alloys or reinforcements of the ductile silver matrix are required. Different reinforcements, e. g. tungsten, tungsten carbide, nickel, cadmium oxide or tin oxide, are used in different sectors of switches. To reach an optimal distribution of these reinforcements, various manufacturing techniques (e. g. powder blending, preform infiltration, wet-chemical methods, internal oxidation are being used for the production of these contact materials. Each of these manufacturing routes offers different advantages and disadvantages. The mechanical alloying process displays a successful and efficient method to produce particle-reinforced metal-matrix composite powders. This contribution presents the obtained fine disperse microstructure of tungsten-particle-reinforced silver composite powders produced by the mechanical alloying process and displays this technique as possible route to provide feedstock powders for subsequent consolidation processes. DOI: http://dx.doi.org/10.5755/j01.ms.20.3.4889

  18. Silver oxide sorbent for carbon dioxide

    Science.gov (United States)

    Colombo, G. V.

    1974-01-01

    Material can be regenerated at least 20 times by heating at 250 C. Sorbent is compatible with environment of high humidity; up to 20% by weight of carbon dioxide can be absorbed. Material is prepared from silver carbonate, potassium hydroxide or carbonate, and sodium silicate.

  19. Biosynthesis of Silver Nanoparticles Using Chenopodium ambrosioides

    Directory of Open Access Journals (Sweden)

    Luis M. Carrillo-López

    2014-01-01

    Full Text Available Biosynthesis of silver nanoparticles (AgNPs was achieved using extract of Chenopodium ambrosioides as a reducer and coating agent at room temperature (25°C. Two molar solutions of AgNO3 (1 mM and 10 mM and five extract volumes (0.5, 1, 2, 3, and 5 mL were used to assess quantity, shape, and size of the particles. The UV-Vis spectra gave surface plasmon resonance at 434–436 nm of the NPs synthesized with AgNO3 10 mM and all extract volumes tested, showing a direct relationship between extract volumes and quantity of particles formed. In contrast, the concentration of silver ions was related negatively to particle size. The smallest (4.9 ± 3.4 nm particles were obtained with 1 mL of extract in AgNO3 10 mM and the larger amount of particles were obtained with 2 mL and 5 mL of extract. TEM study indicated that the particles were polycrystalline and randomly oriented with a silver structure face centered cubic (fcc and fourier transform infrared spectroscopy (FTIR indicated that disappearance of the –OH group band after bioreduction evidences its role in reducing silver ions.

  20. Synthesis and Study of Silver Nanoparticles

    Science.gov (United States)

    Soloman, Sally D.; Bahadory, Mozghan; Jeyarajasingam, Aravindan V.; Rutkowsky, Susan A.; Boritz, Charles; Mulfinger, Lorraine

    2007-01-01

    A laboratory experiment was conducted in which the students synthesized yellow colloidal silver, estimate particle size using visible spectroscopy and studied aggregation effects. The students were thus introduced to nanotechnology along with other topics such as redox chemistry, limiting and excess reactants, spectroscopy and atomic size.

  1. Microscopical Examination of Ancient Silver Coins

    International Nuclear Information System (INIS)

    The microstructure of three silver coins of the IIId century B.C. from the Illyrian king Monounios, the ancient Greek city of Dyrrachion and of Korkyra was studied with XRF and microscopy. From this investigation it turned out that these coins have different chemical composition and microstructure that imply different minting method

  2. Silver doped catalysts for treatment of exhaust

    Energy Technology Data Exchange (ETDEWEB)

    Park, Paul Worn (Peoria, IL); Hester, Virgil Raymond (Edelstein, IL); Ragle, Christie Susan (Havana, IL); Boyer, Carrie L. (Shiloh, IL)

    2009-06-02

    A method of making an exhaust treatment element includes washcoating a substrate with a slurry that includes a catalyst support material. At least some of the catalyst support material from the slurry may be transferred to the substrate, and silver metal (Ag) is dispersed within the catalyst support material.

  3. Silver nanoparticle toxicity in Drosophila: size does matter

    Directory of Open Access Journals (Sweden)

    Deborah J Gorth

    2011-02-01

    Full Text Available Deborah J Gorth1, David M Rand2, Thomas J Webster11School of Engineering, 2Department of Ecology and Evolutionary Biology, Brown University, Providence, RI, USABackground: Consumer nanotechnology is a growing industry. Silver nanoparticles are the most common nanomaterial added to commercially available products, so understanding the influence that size has on toxicity is integral to the safe use of these new products. This study examined the influence of silver particle size on Drosophila egg development by comparing the toxicity of both nanoscale and conventional-sized silver particles.Methods: The toxicity assays were conducted by exposing Drosophila eggs to particle concentrations ranging from 10 ppm to 100 ppm of silver. Size, chemistry, and agglomeration of the silver particles were evaluated using transmission electron microscopy, X-ray photoelectron spectroscopy, and dynamic light scattering.Results: This analysis confirmed individual silver particle sizes in the ranges of 20–30 nm, 100 nm, and 500–1200 nm, with similar chemistry. Dynamic light scattering and transmission electron microscope data also indicated agglomeration in water, with the transmission electron microscopic images showing individual particles in the correct size range, but the dynamic light scattering z-average sizes of the silver nanoparticles were 782 ± 379 nm for the 20–30 nm silver nanoparticles, 693 ± 114 nm for the 100 nm silver nanoparticles, and 508 ± 32 nm for the 500–1200 nm silver particles. Most importantly, here we show significantly more Drosophila egg toxicity when exposed to larger, nonnanometer silver particles. Upon exposure to silver nanoparticles sized 20–30 nm, Drosophila eggs did not exhibit a statistically significant (P < 0.05 decrease in their likelihood to pupate, but eggs exposed to larger silver particles (500–1200 nm were 91% ± 18% less likely to pupate. Exposure to silver nanoparticles reduced the percentage of pupae able

  4. μ3-Oxido-tris{dichlorido[1,3-bis(1,3,5-trimethylphenylimidazol-2-ylidene]gold(III} bis(trifluoromethanesulfonylimide–[bis(trifluoromethanesulfonylimide]silver(I (1/2

    Directory of Open Access Journals (Sweden)

    Marek Pažický

    2010-07-01

    Full Text Available The unusual trinuclear AuIII oxide title complex, [Au3Cl6O(C21H24N23](C2F6NO4S2·2[Ag(C2F6NO4S2], is the side product of the reaction of [1,3-bis(1,3,5-trimethylphenylimidazol-2-ylidene]dichloridophenylgold(III with silver bis(trifluoromethanesulfonylimide in the presence of traces of water. In contrast to corresponding AuI complexes, the core structure of the title compound is planar. Two silver(I bis(trifluoromethanesulfonylimide units are loosely bound to the complex cation. Here the silver atoms, disordered over two positions in a 0.870 (2:0.130 (2 ratio, interact either with the lone pairs of three chlorine ligands or two chlorine ligands and one edge of the mesityl π-system. The crystal under investigation was a partial racemic twin.

  5. Hydration Structure of the Quaternary Ammonium Cations

    KAUST Repository

    Babiaczyk, Wojtek Iwo

    2010-11-25

    Two indicators of the hydropathicity of small solutes are introduced and tested by molecular dynamics simulations. These indicators are defined as probabilities of the orientation of water molecules\\' dipoles and hydrogen bond vectors, conditional on a generalized distance from the solute suitable for arbitrarily shaped molecules. Using conditional probabilities, it is possible to distinguish features of the distributions in close proximity of the solute. These regions contain the most significant information on the hydration structure but cannot be adequately represented by using, as is usually done, joint distance-angle probability densities. Our calculations show that using our indicators a relative hydropathicity scale for the interesting test set of the quaternary ammonium cations can be roughly determined. © 2010 American Chemical Society.

  6. Univalent-cation-elicited acidification by yeasts.

    Science.gov (United States)

    Kotyk, A; Georghiou, G

    1994-08-01

    Addition of univalent cations to sugar-metabolizing Saccharomyces cerevisiae, Schizosaccharomyces pombe and Lodderomyces elongisporus brought about a powerful acidification of the external medium with rates up to nearly 20 nmol H+ per min per mg dry wt. in S. cerevisiae, over 15 nmol in S. pombe, and 4.7 nmol in L. elongisporus. These rates were as much as 20 times, 5.5 times and 10.3 times, respectively. higher than in the absence of K+. Use of galactose-induced cells, of H(+)-ATPase-deficient mutants and observations over the entire growth curve indicated that the K+ effect on H+ extrusion is not connected with the H(+)-ATPase function as such but rather depends on metabolic reactions producing ATP. The effect has apparently nothing to do with the electrical potential across the plasma membrane. PMID:7804140

  7. Retention of Cationic Starch onto Cellulose Fibres

    Science.gov (United States)

    Missaoui, Mohamed; Mauret, Evelyne; Belgacem, Mohamed Naceur

    2008-08-01

    Three methods of cationic starch titration were used to quantify its retention on cellulose fibres, namely: (i) the complexation of CS with iodine and measurement of the absorbency of the ensuing blue solution by UV-vis spectroscopy; (ii) hydrolysis of the starch macromolecules followed by the conversion of the resulting sugars to furan-based molecules and quantifying the ensuing mixture by measuring their absorbance at a Ι of 490 nm, using the same technique as previous one and; finally (iii) hydrolysis of starch macromolecules by trifluoro-acetic acid and quantification of the sugars in the resulting hydrolysates by high performance liquid chromatography. The three methods were found to give similar results within the range of CS addition from 0 to 50 mg per g of cellulose fibres.

  8. Capturing dynamic cation hopping in cubic pyrochlores

    Science.gov (United States)

    Brooks Hinojosa, Beverly; Asthagiri, Aravind; Nino, Juan C.

    2011-08-01

    In direct contrast to recent reports, density functional theory predicts that the most stable structure of Bi2Ti2O7 pyrochlore is a cubic Fd3¯m space group by accounting for atomic displacements. The displaced Bi occupies the 96g(x,x,z) Wyckoff position with six equivalent sites, which create multiple local minima. Using nudged elastic band method, the transition states of Bi cation hopping between equivalent minima were investigated and an energy barrier between 0.11 and 0.21 eV was determined. Energy barriers associated with the motion of Bi between equivalent sites within the 96g Wyckoff position suggest the presence of dielectric relaxation in Bi2Ti2O7.

  9. Interaction of actinide cations with synthetic polyelectrolytes

    International Nuclear Information System (INIS)

    The binding of Am+3, Th+4 and UO2+2 to polymaleic acid, polyethylenemaleic acid and polymethylvinylethermaleic acid has been measured by a solvent extraction technique at 250C and either 0.02 or 0.10 M ionic strength. The solutions were buffered over a pH range such that the percent of carboxylate groups ionized ranged from 25 to 74%. The binding was described by two constants, β1 and β2, which were evaluated after correction for complexation of the actinide cations by acetate and hydrolysis. For comparable degrees of ionization, all three polyelectrolytes showed similar binding strengths. In general, these results indicated that the binding of actinides to these synthetic polyelectrolytes is basically similar to that of natural polyelectrolytes such as humic and fulvic acids. (orig.)

  10. Substitution Pattern Reverses the Fluorescence Response of Coumarin Glycoligands upon Coordination with Silver (I)

    Science.gov (United States)

    Shi, De-Tai; Wei, Xiao-Li; Sheng, Yayun; Zang, Yi; He, Xiao-Peng; Xie, Juan; Liu, Guixia; Tang, Yun; Li, Jia; Chen, Guo-Rong

    2014-03-01

    Development of sugar-based fluorescence (FL) chemo-probes is of much interest since sugars are biocompatible, water-soluble and structurally rigid natural starting materials. We report here that fluorescent glycoligands with two triazolyl coumarin moieties installed onto the different positions of an identical glucosyl nucleus exert completely reversed optical response to a metal ion. C3,4-, C2,3- and C4,6-di-substituted coumarin glucosides synthesized by a click reaction similarly showed a selective FL variation in the presence of silver (I) among a range of metal cations in an aqueous solution. However, the variation was determined to be converse: the FL of the C3,4-ligand was quenched whereas that of the C2,3/C4,6-ligand tangibly enhanced. FL and NMR titrations suggested that this divergence was due to the distinct complexation modes of the conformationally constrained ligands with the ion. The optimal motifs of the ligand-ion complexation were predicted by a computational simulation. Finally, the C2,3-ligand was determined to be of low cytotoxicity and applicable in the FL imaging of silver ions internalized by live cells.

  11. Facile one-pot synthesis of gold and silver nanocatalysts using edible coconut oil.

    Science.gov (United States)

    Meena Kumari, M; Philip, Daizy

    2013-07-01

    The use of edible oil for the synthesis of metal nanoparticles by wet chemical method is reported for the first time. The paper presents an environmentally benign bottom up approach for the synthesis of gold and silver nanoparticles using edible coconut oil at 373 K. The formation of silver nanoparticles is signaled by the brownish yellow color and that of gold nanoparticles by the purple color. Fine control over the nanoparticle size and shape from triangular to nearly spherical is achieved by varying the quantity of coconut oil. The nanoparticles have been characterized by UV-Visible, Transmission Electron Microscopy and X-ray Diffraction. The chemical interaction of capping agents with metal nanoparticles is manifested using Fourier Transform Infrared Spectroscopy. The stable and crystalline nanoparticles obtained using this simple method show remarkable size-dependent catalytic activity in the reduction of the cationic dye methylene blue (MB) to leuco methylene blue (LMB). The first order rate constants calculated uphold the size dependent catalytic activity of the synthesized nanoparticles.

  12. Biocidal Activity of Plasma Modified Electrospun Polysulfone Mats Functionalized with Polyethyleneimine-Capped Silver Nanoparticles

    KAUST Repository

    Schiffman, Jessica D.

    2011-11-01

    The incorporation of silver nanoparticles (AgNPs) into polymeric nanofibers has attracted a great deal of attention due to the strong antimicrobial activity that the resulting fibers exhibit. However, bactericidal efficacy of AgNP-coated electrospun fibrous mats has not yet been demonstrated. In this study, polysulfone (PSf) fibers were electrospun and surface-modified using an oxygen plasma treatment, which allowed for facile irreversible deposition of cationically charged polyethyleneimine (PEI)-AgNPs via electrostatic interactions. The PSf-AgNP mats were characterized for relative silver concentration as a function of plasma treatment time using ICP-MS and changes in contact angle. Plasma treatment of 60 s was the shortest time required for maximum loss of bacteria (Escherichia coli) viability. Time-dependent bacterial cytotoxicity studies indicate that the optimized PSf-AgNP mats exhibit a high level of inactivation against both Gram negative bacteria, Escherichia coli, and Gram positive bacteria, Bacillus anthracis and Staphylococcus aureus. © 2011 American Chemical Society.

  13. Facile one-pot synthesis of gold and silver nanocatalysts using edible coconut oil

    Science.gov (United States)

    Meena Kumari, M.; Philip, Daizy

    2013-07-01

    The use of edible oil for the synthesis of metal nanoparticles by wet chemical method is reported for the first time. The paper presents an environmentally benign bottom up approach for the synthesis of gold and silver nanoparticles using edible coconut oil at 373 K. The formation of silver nanoparticles is signaled by the brownish yellow color and that of gold nanoparticles by the purple color. Fine control over the nanoparticle size and shape from triangular to nearly spherical is achieved by varying the quantity of coconut oil. The nanoparticles have been characterized by UV-Visible, Transmission Electron Microscopy and X-ray Diffraction. The chemical interaction of capping agents with metal nanoparticles is manifested using Fourier Transform Infrared Spectroscopy. The stable and crystalline nanoparticles obtained using this simple method show remarkable size-dependent catalytic activity in the reduction of the cationic dye methylene blue (MB) to leuco methylene blue (LMB). The first order rate constants calculated uphold the size dependent catalytic activity of the synthesized nanoparticles.

  14. Silver-mediated base pairings: towards dynamic DNA nanostructures with enhanced chemical and thermal stability

    Science.gov (United States)

    Swasey, Steven M.; Gwinn, Elisabeth G.

    2016-04-01

    The thermal and chemical fragility of DNA nanomaterials assembled by Watson–Crick (WC) pairing constrain the settings in which these materials can be used and how they can be functionalized. Here we investigate use of the silver cation, Ag+, as an agent for more robust, metal-mediated self-assembly, focusing on the simplest duplex building blocks that would be required for more elaborate Ag+–DNA nanostructures. Our studies of Ag+-induced assembly of non-complementary DNA oligomers employ strands of 2–24 bases, with varied base compositions, and use electrospray ionization mass spectrometry to determine product compositions. High yields of duplex products containing narrowly distributed numbers of Ag+ can be achieved by optimizing solution conditions. These Ag+-mediated duplexes are stable to at least 60 mM Mg2+, higher than is necessary for WC nanotechnology schemes such as tile assemblies and DNA origami, indicating that sequential stages of Ag+-mediated and WC-mediated assembly may be feasible. Circular dichroism spectroscopy suggests simple helical structures for Ag+-mediated duplexes with lengths to at least 20 base pairs, and further indicates that the structure of cytosine-rich duplexes is preserved at high urea concentrations. We therefore propose an approach towards dynamic DNA nanomaterials with enhanced thermal and chemical stability through designs that combine sturdy silver-mediated ‘frames’ with WC paired ‘pictures’.

  15. Symmetry breaking in ligand-protected gold clusters probed by nonlinear optics

    Science.gov (United States)

    van Steerteghem, Nick; van Cleuvenbergen, Stijn; Deckers, Steven; Kumara, Chanaka; Dass, Amala; Häkkinen, Hannu; Clays, Koen; Verbiest, Thierry; Knoppe, Stefan

    2016-06-01

    The first hyperpolarizabilities of [Au25(SR)18]-1/0 and Au38(SR)24 clusters were determined by Hyper-Rayleigh Scattering. A strong dependence on the molecular symmetry was observed, and we explore two strategies to destroy the center of inversion in [Au25(SR)18]-1/0, protection by chiral ligands and alloying of the cluster with silver. This may open new avenues to applications of Au : SR clusters in second-order nonlinear optics.The first hyperpolarizabilities of [Au25(SR)18]-1/0 and Au38(SR)24 clusters were determined by Hyper-Rayleigh Scattering. A strong dependence on the molecular symmetry was observed, and we explore two strategies to destroy the center of inversion in [Au25(SR)18]-1/0, protection by chiral ligands and alloying of the cluster with silver. This may open new avenues to applications of Au : SR clusters in second-order nonlinear optics. Electronic supplementary information (ESI) available: Synthesis and characterization of the clusters, details on HRS measurements and DFT calculations. See DOI: 10.1039/c6nr02251k

  16. Antiviral effect of cationic compounds on bacteriophages

    Directory of Open Access Journals (Sweden)

    Mai Huong eChatain-Ly

    2013-03-01

    Full Text Available The antiviral activity of several cationic compounds - cetytrimethylammonium (CTAB, chitosan, nisin and lysozyme - was investigated on the bacteriophage c2 (DNA head and non-contractile tail infecting Lactococcus strains and the bacteriophage MS2 (F-specific RNA infecting E.coli. Firstly, these activities were evaluated in a phosphate buffer pH 7- 10 mM. The CTAB had a virucidal effect on the Lactococcus bacteriophages, but not on the MS2. After 1 min of contact with 0.125 mM CTAB, the c2 population was reduced from 6 log(pfu/mL to 1,5 log(pfu/mL and completely deactivated at 1 mM. On the contrary, chitosan inhibited the MS2 more than it did the bacteriophages c2. No antiviral effect was observed for the nisin or the lysozyme on bacteriophages after 1 min of treatment. A 1 and 2.5 log reduction was respectively observed for nisin and lysozyme when the treatment time increased (5 or 10 min. These results showed that the antiviral effect depended both on the virus and structure of the antimicrobial compounds. The antiviral activity of these compounds was also evaluated in different physico-chemical conditions and in complex matrices. The antiviral activity of CTAB was impaired in acid pH and with an increase of the ionic strength. These results might be explained by the electrostatic interactions between cationic compounds and negatively charged particles such as bacteriophages or other compounds in a matrix. Milk proved to be protective suggesting the components of food could interfere with antimicrobial compounds.

  17. Versatile synthesis of PHMB-stabilized silver nanoparticles and their significant stimulating effect on fodder beet (Beta vulgaris L.).

    Science.gov (United States)

    Gusev, Alexander А; Kudrinsky, Alexey A; Zakharova, Olga V; Klimov, Alexey I; Zherebin, Pavel M; Lisichkin, George V; Vasyukova, Inna A; Denisov, Albert N; Krutyakov, Yurii A

    2016-05-01

    Silver nanoparticles (AgNPs) are well-known bactericidal agents. However, information about the influence of AgNPs on the morphometric parameters and biochemical status of most important agricultural crops is limited. The present study reports the influence of AgNPs stabilized with cationic polymer polyhexamethylene biguanide hydrochloride (PHMB) on growth, development, and biochemical status of fodder beet Beta vulgaris L. under laboratory and greenhouse conditions. PHMB-stabilized AgNPs were obtained via sodium borohydride reduction of silver nitrate in an aqueous solution. The average diameter of thus prepared AgNPs was 10 nm. It appears that the results of experiments with laboratory-grown beets in the nanosilver-containing medium, where germination of seeds and growth of roots were suppressed, do not correlate with the results of greenhouse experiments. The observed growth-stimulating action of PHMB-stabilized AgNPs can be explained by the change of activity of oxidases and, consequently, by the change of auxins amount in plant tissues. In beets grown in the presence of PHMB-stabilized AgNPs no negative deviations of biological parameters from normal values were registered. Furthermore, the SEM/EDS examination revealed no presence of silver in the tissues of the studied plants. PMID:26952409

  18. Effects of electrolytes and surfactants on the morphology and stability of advanced silver nano-materials

    Energy Technology Data Exchange (ETDEWEB)

    Obaid, Abdullah Yousif; AL-Thabaiti, Shaeel Ahmed; El-Mossalamy, E.H. [Department of Chemistry, Faculty of Science, King Abdulaziz University, P.O. Box 80203, Jeddah 21413 (Saudi Arabia); Hussain, Javed Ijaz [Nano-science Research Lab, Department of Chemistry, Jamia Millia Islamia (Central University), New Delhi 110 025 (India); Khan, Zaheer, E-mail: drkhanchem@yahoo.co.in [Nano-science Research Lab, Department of Chemistry, Jamia Millia Islamia (Central University), New Delhi 110 025 (India)

    2013-03-15

    Highlights: ► Stoichiometric ratio of S{sub 2}O{sub 3}{sup 2−} and Ag{sup +} ions are responsible to the formation of prefect transparent yellow colored silver sol. ► Higher S{sub 2}O{sub 3}{sup 2−} concentrations has damping effect. ► Head group of the surfactants and nature of the electrolytes have significant effect on the stability of silver nanoparticles. - Abstract: The impact of electrolytes, stabilizing and/or capping agents on morphology of colloidal silver nano-materials (AgNPs) has been studied spectroscopically. Sodium thiosulfate acts as reducing-, stabilizing- and damping-agents. Stoichiometric ratios of S{sub 2}O{sub 3}{sup 2−} and Ag{sup +} ions were responsible to the formation stable and prefect transparent dark yellow colored AgNPs. The S{sub 2}O{sub 3}{sup 2−}-stabilized AgNPs were significantly more stable in inorganic electrolytes (NaNO{sub 3}, Na{sub 2}SO{sub 4}, Na{sub 2}CO{sub 3} and KBr). S{sub 2}O{sub 3}{sup 2−} is adsorbed more strongly than the used other anions. The addition of cetyltrimethylammonium bromide (CTAB) and sodium dodecylsulfate (SDS) has significant effects on the absorbance of S{sub 2}O{sub 3}{sup 2−}-stabilized AgNPs which can be rationalized in terms of electrostatic attraction and repulsion between the adsorbed S{sub 2}O{sub 3}{sup 2−} ions on to the surface of AgNPs and cationic and/or anionic head groups of used surfactants, respectively. Transmission electron microscopy images suggest that AgNPs are polydispersed, spherical and exhibiting an interesting irregular morphology.

  19. Star clusters and associations

    International Nuclear Information System (INIS)

    All 33 papers presented at the symposium were inputted to INIS. They dealt with open clusters, globular clusters, stellar associations and moving groups, and local kinematics and galactic structures. (E.S.)

  20. Highly fluorescent silver nanoclusters in alumina-silica composite optical fiber

    Energy Technology Data Exchange (ETDEWEB)

    Halder, A.; Chattopadhyay, R.; Majumder, S.; Paul, M. C.; Das, S.; Bhadra, S. K., E-mail: skbhadra@cgcri.res.in [Fiber Optics and Photonics Division, CSIR-Central Glass and Ceramic Research Institute, 196, Raja S. C. Mullick Road, Kolkata 700032 (India); Bysakh, S.; Unnikrishnan, M. [Material Characterization Division, CSIR-Central Glass and Ceramic Research Institute, 196, Raja S. C. Mullick Road, Kolkata 700032 (India)

    2015-01-05

    An efficient visible fluorescent optical fiber embedded with silver nanoclusters (Ag-NCs) having size ∼1 nm, uniformly distributed in alumina-silica composite core glass, is reported. Fibers are fabricated in a repetitive controlled way through modified chemical vapour deposition process associated with solution doping technique. Fibers are drawn from the transparent preforms by conventional fiber drawing process. Structural characteristics of the doped fibers are studied using transmission electron microscopy and electron probe micro analysis. The oxidation state of Ag within Ag-NCs is investigated by X-ray photo electron spectroscopy. The observed significant fluorescence of the metal clusters in fabricated fibers is correlated with electronic model. The experimentally observed size dependent absorption of the metal clusters in fabricated fibers is explained with the help of reported results calculated by ab-initio density functional theory. These optical fibers may open up an opportunity of realizing tunable wavelength fiber laser without the help of rare earth elements.