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Sample records for metals silver mercury

  1. Xenobiotic metal-induced autoimmunity: mercury and silver differentially induce antinucleolar autoantibody production in susceptible H-2s, H-2q and H-2f mice

    PubMed Central

    Hansson, M; Abedi-Valugerdi, M

    2003-01-01

    Xenobiotic-metals such as mercury (Hg) and silver (Ag) induce an H-2 linked antinucleolar autoantibody (ANolA) production in susceptible mice. The mechanism for induction of ANolA synthesis is not well understood. However, it has been suggested that both metals interact with nucleolar proteins and reveal cryptic self-peptides to nontolerant autoreactive T cells, which in turn stimulate specific autoreactive B cells. In this study, we considered this suggestion and asked if mercury and silver display, if not identical, similar cryptic self-peptides, they would induce comparable ANolA responses in H-2 susceptible mice. We analysed the development of ANolA production in mercury- and/or silver-treated mice of H-2s, H-2q and H-2f genotypes. We found that while mercury stimulated ANolA synthesis in all strains tested, silver induced ANolA responses of lower magnitudes in only H-2s and H-2q mice, but not in H-2f mice. Resistance to silver in H-2f mice was independent of the dosage/time-period of silver-treatment and non-H-2 genes. Further studies showed that F1 hybrid crosses between silver-susceptible A.SW (H-2s) and -resistant A.CA (H-2f) mice were resistant to silver, but not mercury with regard to ANolA production. Additionally, the magnitudes of mercury-induced ANolA responses in the F1 hybrids were lower than those of their parental strains. The above differential ANolA responses to mercury and silver can be explained by various factors, including the different display of nucleolar cryptic peptides by these xenobiotics, determinant capture and coexistence of different MHC molecules. Our findings also suggest that the ability of a xenobiotic metal merely to create cryptic self-peptides may not be sufficient for the induction of an ANolA response. PMID:12605692

  2. Mercury

    MedlinePlus

    Mercury is an element that is found in air, water and soil. It has several forms. Metallic mercury is a shiny, silver-white, ... colorless, odorless gas. It also combines with other elements to form powders or crystals. Mercury is in ...

  3. Mercury Quick Facts: Health Effects of Mercury Exposure

    MedlinePlus

    Mercury Quick Facts Health Effects of Mercury Exposure What is Elemental Mercury? Elemental (metallic) mercury is the shiny, silver-gray metal found in thermometers, barometers, and thermostats and other ...

  4. Gastrointestinal absorption of metallic mercury.

    PubMed

    Sandborgh-Englund, Gunilla; Einarsson, Curt; Sandström, Magnus; Ekstrand, Jan

    2004-09-01

    The absorption of mercury from the gastrointestinal systems of 7 subjects, of whom none had any amalgam fillings, was examined in this study. The authors obtained quantitative information about mercury concentration in plasma and duodenal fluid after the gastrointestinal systems of the subjects were exposed to liquid elemental mercury enclosed in rubber balloons (i.e., approximately 20 g of mercury), using a standard procedure followed for the sampling of bile. Plasma samples were collected prior to exposure, as well as up to 10 d following exposure, and duodenal fluid was collected 1 h, 2 h, 4 h, and 6 h during the intubation process. The authors studied the kinetics of dissolution in vitro by leaching elemental liquid mercury and mercuric chloride. The results of this study supported the hypothesis that metallic mercury is oxidized in the gastrointestinal tract. In addition, the authors determined that duodenal intubation, while using liquid metallic mercury in rubber bags, resulted in the diffusion of minor amounts of atomic elemental mercury through the rubber walls. The absorbed amount of mercury that reached the central circulation was comparable to a daily dose of mercury from dental amalgam in the amalgam-bearing population. PMID:16381485

  5. MOD silver metallization for photovoltaics

    NASA Technical Reports Server (NTRS)

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

    1984-01-01

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

  6. Copper, silver, gold and zinc, cadmium, mercury oxides and hydroxides

    SciTech Connect

    Dirkse, T.P.

    1986-01-01

    This book provides a compilation of solubility data published up to 1984, including evaluations of the data. Data are presented on the following: copper (I) oxide; copper (II) oxide and hydroxide; silver (I) oxide; silver (II) oxide; gold (III) hydroxide; zinc oxide and hydroxide; cadmium oxide and hydroxide; and mercury (II) oxide.

  7. MOD silver metallization for photovoltaics

    NASA Technical Reports Server (NTRS)

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

    1985-01-01

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

  8. Process for making silver metal filaments

    DOEpatents

    Bamberger, Carlos E.

    1997-01-01

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

  9. Process for making silver metal filaments

    SciTech Connect

    Bamberger, C.E.

    1997-05-06

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

  10. The Hydrothermal Chemistry of Gold, Arsenic, Antimony, Mercury and Silver

    SciTech Connect

    Bessinger, Brad; Apps, John A.

    2003-03-23

    A comprehensive thermodynamic database based on the Helgeson-Kirkham-Flowers (HKF) equation of state was developed for metal complexes in hydrothermal systems. Because this equation of state has been shown to accurately predict standard partial molal thermodynamic properties of aqueous species at elevated temperatures and pressures, this study provides the necessary foundation for future exploration into transport and depositional processes in polymetallic ore deposits. The HKF equation of state parameters for gold, arsenic, antimony, mercury, and silver sulfide and hydroxide complexes were derived from experimental equilibrium constants using nonlinear regression calculations. In order to ensure that the resulting parameters were internally consistent, those experiments utilizing incompatible thermodynamic data were re-speciated prior to regression. Because new experimental studies were used to revise the HKF parameters for H2S0 and HS-1, those metal complexes for which HKF parameters had been previously derived were also updated. It was found that predicted thermodynamic properties of metal complexes are consistent with linear correlations between standard partial molal thermodynamic properties. This result allowed assessment of several complexes for which experimental data necessary to perform regression calculations was limited. Oxygen fugacity-temperature diagrams were calculated to illustrate how thermodynamic data improves our understanding of depositional processes. Predicted thermodynamic properties were used to investigate metal transport in Carlin-type gold deposits. Assuming a linear relationship between temperature and pressure, metals are predicted to predominantly be transported as sulfide complexes at a total aqueous sulfur concentration of 0.05 m. Also, the presence of arsenic and antimony mineral phases in the deposits are shown to restrict mineralization within a limited range of chemical conditions. Finally, at a lesser aqueous sulfur

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

    SciTech Connect

    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.

  12. Exploiting the higher specificity of silver amalgamation: selective detection of mercury(II) by forming Ag/Hg amalgam.

    PubMed

    Deng, Li; Ouyang, Xiangyuan; Jin, Jianyu; Ma, Cheng; Jiang, Ying; Zheng, Jing; Li, Jishan; Li, Yinhui; Tan, Weihong; Yang, Ronghua

    2013-09-17

    Heavy metal ion pollution poses severe risks in human health and the environment. Driven by the need to detect trace amounts of mercury, this article demonstrates, for the first time, that silver/mercury amalgamation, combining with DNA-protected silver nanoparticles (AgNPs), can be used for rapid, easy and reliable screening of Hg(2+) ions with high sensitivity and selectivity over competing analytes. In our proposed approach, Hg(2+) detection is achieved by reducing the mercury species to elemental mercury, silver atoms were chosen as the mercury atoms' acceptors by forming Ag/Hg amalgam. To signal fluorescently this silver amalgamation event, a FAM-labeled ssDNA was employed as the signal reporter. AgNPs were grown on the DNA strand that resulted in greatly quenching the FAM fluorescence. Formation of Ag/Hg amalgam suppresses AgNPs growth on the DNA, leading to fluorescence signal increase relative to the fluorescence without Hg(2+) ions, as well as marked by fluorescence quenching. This FAM fluorescence enhancement can be used for detection of Hg(2+) at the a few nanomolar level. Moreover, due to excellent specificity of silver amalgamation with mercury, the sensing system is highly selective for Hg(2+) and does not respond to other metal ions with up to millimolar concentration levels. This sensor is successfully applied to determination of Hg(2+) in tap water, spring water and river water samples. The results shown herein have important implications in the development of new fluorescent sensors for the fast, easy, and selective detection and quantification of Hg(2+) in environmental and biological samples. PMID:23937672

  13. Reaction of mercury with silver-tin dental amalgam alloy.

    PubMed

    Abbott, J R; Miller, D R; Netherway, D J

    1982-09-01

    Electron diffraction evidence confirming the ordered orthorhombic crystal structure of the gamma phase of the silver-tin system has been obtained, and it has been established by optical metallography that an alloy with a composition corresponding to the dental amalgam alloy formula Ag3Sn (i.e., 26.85 wt % Sn) lies outside the single gamma phase field and in the duplex (gamma + Sn) phase field adjacent to it. Studies of the mechanism of the hardening reaction of single crystals of homogeneous gamma phase alloys with mercury were carried out using both scanning and transmission electron microscopy. Mercury attack occurred preferentially along well-defined planes in the single crystals. Using electron channeling and trace analysis techniques these planes of preferential attack were found to be [010] and [011], and from transmission electron microscopy of thin foils these were shown to be slip bands and deformation twins, respectively. In bicrystals of gamma phase material, preferential attack also occurred along grain boundaries. Similar preferential mercury attack, leading to the development of deep planar intrusions into the gamma phase material, was observed in an experimental dental amalgam prepared from a lathe-cut homogeneous gamma phase amalgam alloy. It is believed that the presence of such features would have important implications for the clinical performance of dental amalgam. PMID:7130210

  14. ELEMENTAL MERCURY IN COPPER, SILVER, AND GOLD ORES: AN UNEXPECTED CONTRIBUTION TO LAKE SUPERIOR SEDIMENTS WITH GLOBAL IMPLICATIONS

    EPA Science Inventory

    Mercury and copper inventories are low in central Lake Superior and increase markedly towards the Keweenaw Peninsula...where copper, mercury, and silver inventories are elevated and highly correlated. High copper, silver, and mercury inventories can be traced back to shoreline st...

  15. Process for making silver metal filaments

    SciTech Connect

    Bamberger, C.E.

    1998-04-01

    This invention relates to a process for making filaments of metal compounds and more particularly to a process for making silver metal filaments. The United States Government has rights to this invention pursuant to Contract No. DE-AC05-8421400 with Lockheed Martin Energy Systems, Inc. awarded by the US Department of Energy.

  16. Irradiation of silver and agar/silver nanoparticles with argon, oxygen glow discharge plasma, and mercury lamp.

    PubMed

    Ahmad, Mahmoud M; Abdel-Wahab, Essam A; El-Maaref, A A; Rawway, Mohammed; Shaaban, Essam R

    2014-01-01

    The irradiation effect of argon, oxygen glow discharge plasma, and mercury lamp on silver and agar/silver nanoparticle samples is studied. The irradiation time dependence of the synthesized silver and agar/silver nanoparticle absorption spectra and their antibacterial effect are studied and compared. In the agar/silver nanoparticle sample, as the irradiation time of argon glow discharge plasma or mercury lamp increases, the peak intensity and the full width at half maximum, FWHM, of the surface plasmon resonance absorption band is increased, however a decrease of the peak intensity with oxygen glow plasma has been observed. In the silver nanoparticle sample, as the irradiation time of argon, oxygen glow discharge plasma or mercury lamp increases, the peak intensity of the surface plasmon resonance absorption band is increased, however, there is no significant change in the FWHM of the surface plasmon resonance absorption band. The SEM results for both samples showed nanoparticle formation with mean size about 50 nm and 40 nm respectively. Throughout the irradiation time with the argon, oxygen glow discharge plasma or mercury lamp, the antibacterial activity of several kinds of Gram-positive and Gram-negative bacteria has been examined. PMID:25184109

  17. Transmission electron microscopy of mercury metal.

    PubMed

    Anjum, Dalaver H; Sougrat, Rachid

    2016-09-01

    Transmission electron microcopy (TEM) analysis of liquid metals, especially mercury (Hg), is difficult to carry out because their specimen preparation poses a daunting task due to the unique surface properties of these metals. This paper reports a cryoTEM study on Hg using a novel specimen preparation technique. Hg metal is mixed with water using sonication and quenched in liquid ethane cryogen. This technique permits research into the morphological, phase and structural properties of Hg at nanoscale dimensions. PMID:27018645

  18. Mercury release of amalgams with various silver contents after exposure to bleaching agent

    PubMed Central

    Bahari, Mahmoud; Alizadeh Oskoee, Parnian; Savadi Oskoee, Siavash; Pouralibaba, Firoz; Morsali Ahari, Ali

    2016-01-01

    Background. Since it is possible for carbamide peroxide (CP) bleaching agent to contact old amalgam restorations, the present in vitro study evaluated the amount of dissolved mercury released from amalgam restorations with various percent-ages of silver content subsequent to the use of 15% CP. Methods. Thirty ANA 2000 amalgam disks with 43.1% silver content and thirty ANA 70 amalgam disks with 69.3% silver content were prepared. In each group, 15 samples were randomly placed in glass tubes containing 15% CP (as experimental groups) and the remaining 15 samples were placed in buffered phosphate solution (as control groups) with the same 3-mL volume for 48 hours. Subsequently, the amount of mercury dissolved in each test tube was measured using Mercury Analyzing System (Cold Vapor Atomic Absorption, MASLO, Shimadzu, Japan). Data was analyzed with two-way ANOVA and a post hoc Tukey test. (α = 0.05). Results. The amount of mercury released after exposure to CP was significantly higher than that released after exposure to buffered phosphate (P < 0.001). In addition, the amount of mercury released from dental amalgam with a silver content of 43% was significantly higher than that released from dental amalgam with a silver content of 69% (P < 0.001). Conclusion. The amount of mercury release is inversely proportional to the silver content of dental amalgam. PMID:27429729

  19. Mercury release of amalgams with various silver contents after exposure to bleaching agent.

    PubMed

    Bahari, Mahmoud; Alizadeh Oskoee, Parnian; Savadi Oskoee, Siavash; Pouralibaba, Firoz; Morsali Ahari, Ali

    2016-01-01

    Background. Since it is possible for carbamide peroxide (CP) bleaching agent to contact old amalgam restorations, the present in vitro study evaluated the amount of dissolved mercury released from amalgam restorations with various percent-ages of silver content subsequent to the use of 15% CP. Methods. Thirty ANA 2000 amalgam disks with 43.1% silver content and thirty ANA 70 amalgam disks with 69.3% silver content were prepared. In each group, 15 samples were randomly placed in glass tubes containing 15% CP (as experimental groups) and the remaining 15 samples were placed in buffered phosphate solution (as control groups) with the same 3-mL volume for 48 hours. Subsequently, the amount of mercury dissolved in each test tube was measured using Mercury Analyzing System (Cold Vapor Atomic Absorption, MASLO, Shimadzu, Japan). Data was analyzed with two-way ANOVA and a post hoc Tukey test. (α = 0.05). Results. The amount of mercury released after exposure to CP was significantly higher than that released after exposure to buffered phosphate (P < 0.001). In addition, the amount of mercury released from dental amalgam with a silver content of 43% was significantly higher than that released from dental amalgam with a silver content of 69% (P < 0.001). Conclusion. The amount of mercury release is inversely proportional to the silver content of dental amalgam. PMID:27429729

  20. Metal-metal bonding using silver/copper nanoparticles

    NASA Astrophysics Data System (ADS)

    Kobayashi, Y.; Maeda, T.; Yasuda, Y.; Morita, T.

    2015-08-01

    A method for producing nanoparticles composed of silver and copper and a metal-metal bonding technique using the silver/copper nanoparticles are proposed. The method consists of three steps. First, copper oxide nanoparticles are produced by mixing Cu(NO3)2 aqueous solution and NaOH aqueous solution. Second, copper metal nanoparticles are fabricated by reducing the copper oxide nanoparticles with hydrazine in the presence of poly(vinylpyrrolidone) (PVP). Third, silver/copper nanoparticles are synthesized by reducing Ag+ ions with hydrazine in the presence of the copper metal nanoparticles. Initial concentrations in the final silver/copper particle colloid, composed of 0.0075 M Cu2+, 0.0025 M Ag+, 1.0 g/L PVP, and 0.6 M hydrazine, produced silver/copper nanoparticles with an average size of 49 nm and a crystal size of 16.8 nm. Discs of copper metal were successfully bonded by the silver/copper nanoparticles under annealing at 400 °C and pressurizing at 1.2 MPa for 5 min in not only hydrogen gas but also nitrogen gas. The shear force required to separate the bonded discs was 22.3 MPa for the hydrogen gas annealing and 14.9 MPa for the nitrogen gas annealing (namely, 66.8 % of that for hydrogen gas annealing).

  1. Metal-metal bonding using silver/copper nanoparticles

    NASA Astrophysics Data System (ADS)

    Kobayashi, Y.; Maeda, T.; Yasuda, Y.; Morita, T.

    2016-08-01

    A method for producing nanoparticles composed of silver and copper and a metal-metal bonding technique using the silver/copper nanoparticles are proposed. The method consists of three steps. First, copper oxide nanoparticles are produced by mixing Cu(NO3)2 aqueous solution and NaOH aqueous solution. Second, copper metal nanoparticles are fabricated by reducing the copper oxide nanoparticles with hydrazine in the presence of poly(vinylpyrrolidone) (PVP). Third, silver/copper nanoparticles are synthesized by reducing Ag+ ions with hydrazine in the presence of the copper metal nanoparticles. Initial concentrations in the final silver/copper particle colloid, composed of 0.0075 M Cu2+, 0.0025 M Ag+, 1.0 g/L PVP, and 0.6 M hydrazine, produced silver/copper nanoparticles with an average size of 49 nm and a crystal size of 16.8 nm. Discs of copper metal were successfully bonded by the silver/copper nanoparticles under annealing at 400 °C and pressurizing at 1.2 MPa for 5 min in not only hydrogen gas but also nitrogen gas. The shear force required to separate the bonded discs was 22.3 MPa for the hydrogen gas annealing and 14.9 MPa for the nitrogen gas annealing (namely, 66.8 % of that for hydrogen gas annealing).

  2. Mercury Production and Use in Colonial Andean Silver Production: Emissions and Health Implications

    PubMed Central

    Hagan, Nicole A.

    2012-01-01

    Background: Colonial cinnabar mining and refining began in Huancavelica, Peru, in 1564. With a local source of mercury, the amalgamation process was adopted to refine silver in Potosí, Bolivia, in the early 1570s. As a result, large quantities of mercury were released into the environment. Objectives: We used archival, primary, and secondary sources to develop the first estimate of mercury emissions from cinnabar refining in Huancavelica and to revise previous estimates of emissions from silver refining in Potosí during the colonial period (1564–1810). Discussion: Although other estimates of historical mercury emissions have recognized Potosí as a significant source, Huancavelica has been overlooked. In addition, previous estimates of mercury emissions from silver refining under-estimated emissions because of unrecorded (contra-band) production and volatilization of mercury during processing and recovery. Archival descriptions document behavioral and health issues during the colonial period that are consistent with known effects of mercury intoxication. Conclusions: According to our calculations, between 1564 and 1810, an estimated 17,000 metric tons of mercury vapor were emitted from cinnabar smelting in Huancavelica, and an estimated 39,000 metric tons were released as vapor during silver refining operations in Potosí. Huancavelica and Potosí combined contributed > 25% of the 196,000 metric tons of mercury vapor emissions in all of Latin America between 1500 and 1800. The historical record is laden with evidence of mercury intoxication consistent with effects recognized today. Our estimates serve as the foundation of investigations of present-day contamination in Huancavelica and Potosí resulting from historical emissions of mercury. PMID:22334094

  3. MOD silver metallization for photovoltaics

    NASA Technical Reports Server (NTRS)

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

    1984-01-01

    Photovoltaic cells require back side metallization and a collector grid system on the front surface. Both front and back surface metallizations should have good adhesion, low contact resistance, low sheet resistance, long term stability, and their deposition methods should not degrade the n-p junction. Advantages and disadvantages of different deposition methods are discussed.

  4. Mercury dispersion in soils of an abandoned lead-zinc-silver mine, San Quintín (Spain)

    NASA Astrophysics Data System (ADS)

    Esbrí, José Maria; Martín-Crespo, T.; Gómez-Ortiz, D.; Monescillo, C. I.; Lorenzo, S.; Higueras, P.

    2010-05-01

    The mine considered on this work, namely San Quintín, is a filonian field with hydrothermal ores exploited during almost fifty years (1887-1934), producing 550.000Tm of galena, 550Tm of silver and 5.000 of sphalerite. Some rewashing works of tailings muds was achieved in recent times (1973-1985), including flotation tests of cinnabar ore from Almadén mines. The main problems remaining on the site are an active acid mine drainage (with pH ~ 2) and heavy metal dispersion on soils including gaseous mercury emissions. We present here results of a survey including soils sampling with mercury analysis and other pedological parameters, as well as determinations of mercury inmission in the atmosphere, using a common sampling grid. Analysis of soils samples has been carried out using an atomic absorption spectrometer AMA254, while air determinations were made by the same technique, using a Lumex RA-915+. The maps have been obtained by means of SURFER 8 software, as well as by ArcGIS software, and puts forward dispersion of mercury from cinnabar ore dump (108 ?g×g-1) to nearby soils (0.3 ?g×g-1 at 700 m of distance). The dispersion of mercury vapor exceed WHO level for chronic exposure (200 ng×m-3) in a small area (250 meters from cinnabar dump).

  5. Smoothing of ultrathin silver films by transition metal seeding

    NASA Astrophysics Data System (ADS)

    Anders, André; Byon, Eungsun; Kim, Dong-Ho; Fukuda, Kentaro; Lim, Sunnie H. N.

    2006-11-01

    The nucleation and coalescence of silver islands on coated glass was investigated by in situ measurements of the sheet resistance. Sub-monolayer amounts of niobium and other transition metals were deposited prior to the deposition of silver. It was found that in some cases, the transition metals lead to coalescence of silver at nominally thinner films with smoother topology. The smoothing or roughening effects by the presence of the transition metal can be explained by kinetically limited transition metal islands growth and oxidation, followed by defect-dominated nucleation of silver.

  6. 49 CFR 173.164 - Mercury (metallic and articles containing mercury).

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... metallic mercury is a component part, such as manometers, pumps, thermometers, switches, etc. (for electron..., leakproof and in sealed metal or plastic units. (2) Thermometers, switches and relays, each containing...

  7. 49 CFR 173.164 - Mercury (metallic and articles containing mercury).

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... metallic mercury is a component part, such as manometers, pumps, thermometers, switches, etc. (for electron..., leakproof and in sealed metal or plastic units. (2) Thermometers, switches and relays, each containing...

  8. Observations of Metallic Species in Mercury's Exosphere

    NASA Technical Reports Server (NTRS)

    Killen, Rosemary M.; Potter, Andrew E.; Vervack, Ronald J., Jr.; Bradley, E. Todd; McClintock, William E.; Anderson, Carrie M.; Burger, Matthew H.

    2010-01-01

    From observations of the metallic species sodium (Na), potassium (K), and magnesium (Mg) in Mercury's exosphere, we derive implications for source and loss processes. All metallic species observed exhibit a distribution and/or line width characteristic of high to extreme temperature - tens of thousands of degrees K. The temperatures of refractory species, including magnesium and calcium, indicate that the source process for the atoms observed in the tail and near-planet exosphere are consistent with ion sputtering and/or impact vaporization of a molecule with subsequent dissociation into the atomic form. The extended Mg tail is consistent with a surface abundance of 5-8% Mg by number, if 30% of impact-vaporized Mg remains as MgO and half of the impact vapor condenses. Globally, ion sputtering is not a major source of Mg, but locally the sputtered source can be larger than the impact vapor source. We conclude that the Na and K in Mercury's exosphere can be derived from a regolith composition similar to that of Luna 16 soil (or Apollo 17 orange glass), in which the abundance by number is 0.0027 (0.0028) for Na and 0.0006 (0.0045) for K.

  9. Mercury sensing and toxicity studies of novel latex fabricated silver nanoparticles.

    PubMed

    Borase, Hemant P; Patil, Chandrashekhar D; Salunkhe, Rahul B; Suryawanshi, Rahul K; Salunke, Bipinchandra K; Patil, Satish V

    2014-11-01

    Safe and eco-friendly alternatives to currently used hazardous chemico-physical methods of silver nanoparticles (AgNPs) synthesis are need of time. Rapid, low cost, selective detection of toxic metals in environmental sample is important to take safety action. Toxicity assessment of engineered AgNPs is essential to avoid its side effects on human and non-target organisms. In the present study, biologically active latex from Euphorbia heterophylla (Poinsettia) was utilized for synthesis of AgNPs. AgNPs was of spherical shape and narrow size range (20-50 nm). Occurrence of elemental silver and crystalline nature of AgNPs was analyzed. Role of latex metabolites in reduction and stabilization of AgNPs was analyzed by FT-IR, protein coagulation test and phytochemical analysis. Latex-synthesized AgNPs showed potential in selective and sensitive detection of toxic mercury ions (Hg(2+)) with limit of detection around 100 ppb. Addition of Hg(2+) showed marked deviation in color and surface plasmon resonance spectra of AgNPs. Toxicity studies on aquatic non-target species Daphnia magna showed that latex-synthesized AgNPs (20.66 ± 1.52% immobilization) were comparatively very less toxic than chemically synthesized AgNPs (51.66 ± 1.52% immobilization). Similarly, comparative toxicity study on human red blood cells showed lower hemolysis (4.46 ± 0.01%) by latex-synthesized AgNPs as compared to chemically synthesized AgNPs causing 6.14 ± 0.01% hemolysis. PMID:24803140

  10. Mercury-impacted scrap metal: Source and nature of the mercury.

    PubMed

    Finster, Molly E; Raymond, Michelle R; Scofield, Marcienne A; Smith, Karen P

    2015-09-15

    The reuse and recycling of industrial solid wastes such as scrap metal is supported and encouraged both internationally and domestically, especially when such wastes can be used as substitutes for raw material. However, scrap metal processing facilities, such as mini-mills, have been identified as a source of mercury (Hg) emissions in the United States. This research aims to better define some of the key issues related to the source and nature of mercury in the scrap metal waste stream. Overall, it is difficult to pinpoint the key mercury sources feeding into scrap metal recycling facilities, quantify their associated mercury concentrations, or determine which chemical forms are most significant. Potential sources of mercury in scrap metal include mercury switches from discarded vehicles, electronic-based scrap from household appliances and related industrial systems, and Hg-impacted scrap metal from the oil and gas industry. The form of mercury associated with scrap metal varies and depends on the source type. The specific amount of mercury that can be adsorbed and retained by steel appears to be a function of both metallurgical and environmental factors. In general, the longer the steel is in contact with a fluid or condensate that contains measurable concentrations of elemental mercury, the greater the potential for mercury accumulation in that steel. Most mercury compounds are thermally unstable at elevated temperatures (i.e., above 350 °C). As such, the mercury associated with impacted scrap is expected to be volatilized out of the metal when it is heated during processing (e.g., shredding or torch cutting) or melted in a furnace. This release of fugitive gas (Hg vapor) and particulates, as well as Hg-impacted bag-house dust and control filters, could potentially pose an occupational exposure risk to workers at a scrap metal processing facility. Thus, identifying and characterizing the key sources of Hg-impacted scrap, and understanding the nature and extent

  11. Practical limitations of ITS-90 from the mercury triple point to the silver freeze point

    SciTech Connect

    Tavener, J. P.; Tavener, S. J.; Tavener, I. F.; Davies, N.

    2013-09-11

    The NPL published a forward to the ITS-90 text as follows:- 'The purpose of the ITS is to define procedures by which certain specified practical thermometers of the required quality can be calibrated in such a way that the values of temperature obtained from them can be precise and reproducible, while at the same time closely approximating the corresponding thermodynamic values.' [1]. The paper investigates the properties of thirty four lots of 6N pure metal used to make cells conforming to ITS-90 from mercury through silver over a period of twenty years. Three hundred individual cells are analysed by the impurities listed and supplied with each lot, melt and freeze curve slopes are also summarised for each lot and depressions calculated. These are then compared to the slopes and depressions suggested in the Supplementary Information for the ITS-90 and in CCT/2000-13 'Optimal Realizations'. Results are summarised, tabulated and discussed. Three lots of the thirty four were found to produce cells outside 6N expectations; however the remaining thirty one lots no matter how well or badly the accompanying certification was presented produced cells that conformed to 6N expectations as suggested in Supplementary Information to ITS-90 and CCT/2000-13.

  12. Mercury emission and behavior in primary ferrous metal production

    NASA Astrophysics Data System (ADS)

    Fukuda, Naomichi; Takaoka, Masaki; Doumoto, Shingo; Oshita, Kazuyuki; Morisawa, Shinsuke; Mizuno, Tadao

    2011-07-01

    Ferrous metal production is thought to be a major mercury emission source because it uses large amounts of coal and iron ore, which contain trace amounts of mercury impurities. However, there is limited information about mercury emissions during the production process. In this study, we focused on the coke-oven process, sintering furnace process, and blast furnace process. We measured the mercury concentration in the raw materials, products, and byproducts to estimate the amount of mercury emitted and to investigate the behavior of mercury during the processes. Average mercury concentrations were 30.8 μg kg -1 in 54 samples of iron ore and 59.9 μg kg -1 in 33 samples of coal. The total mercury used for ferrous metal production in Japan was estimated to be 8.45 tons in 2005, with 4.07 tons from iron ore, 3.76 tons from coal, and 0.478 tons from limestone. Emissions from the sintering process accounted for more than 90% of the total emissions, and mercury in the exhaust gas was reduced using an activated coke tower and desulfurization equipment installed downstream of an electrostatic precipitator. When byproduct gas generated from coke-oven and blast furnace processes were included, mercury emissions estimates based on actual measurements were 4.08 tons y -1 (in 2005). Thus, about 50% of the mercury input in ferrous metal production was emitted to the atmosphere. The emission factor was calculated as 0.0488 g Hg ton -1 for crude steel production. The introduction of activated coke tower or desulfurization equipment in sintering furnace facilities would reduce mercury emissions.

  13. 49 CFR 173.164 - Mercury (metallic and articles containing mercury).

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... mercury is a component part, such as manometers, pumps, thermometers, switches, etc. (for electron tubes..., leakproof and in sealed metal or plastic units. (2) When transported as cargo, thermometers, switches...

  14. 49 CFR 173.164 - Mercury (metallic and articles containing mercury).

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... mercury is a component part, such as manometers, pumps, thermometers, switches, etc. (for electron tubes..., leakproof and in sealed metal or plastic units. (2) When transported as cargo, thermometers, switches...

  15. Environmental impact of mercury and other heavy metals

    NASA Astrophysics Data System (ADS)

    Lindqvist, Oliver

    The environmental impact of heavy metals is reviewed. One significant source of emissions of heavy metals to air is waste incineration. Consumer batteries contributes significantly to this problem, as well as to heavy metal leakage to groundwater from landfill deposits. The situation in Sweden is used as an example to describe how the deposition from the atmosphere still is increasing the load of heavy metals, like mercury, cadmium and lead, in top soils and aquatic sediments. Critical factors and effect levels for Hg, Cd, Pb, Cu, Zn and As are discussed. Specific questions like mercury contents in present battery waste and heavy metal contents in new and future secondary batteries are addressed.

  16. Method for Reduction of Silver Biocide Plating on Metal Surfaces

    NASA Technical Reports Server (NTRS)

    Steele, John; Nalette, Timothy; Beringer, Durwood

    2013-01-01

    Silver ions in aqueous solutions (0.05 to 1 ppm) are used for microbial control in water systems. The silver ions remain in solution when stored in plastic containers, but the concentration rapidly decreases to non-biocidal levels when stored in metal containers. The silver deposits onto the surface and is reduced to non-biocidal silver metal when it contacts less noble metal surfaces, including stainless steel, titanium, and nickel-based alloys. Five methods of treatment of contact metal surfaces to deter silver deposition and reduction are proposed: (1) High-temperature oxidation of the metal surface; (2) High-concentration silver solution pre-treatment; (3) Silver plating; (4) Teflon coat by vapor deposition (titanium only); and (5) A combination of methods (1) and (2), which proved to be the best method for the nickel-based alloy application. The mechanism associated with surface treatments (1), (2), and (5) is thought to be the development of a less active oxide layer that deters ionic silver deposition. Mechanism (3) is an attempt to develop an equilibrium ionic silver concentration via dissolution of metallic silver. Mechanism (4) provides a non-reactive barrier to deter ionic silver plating. Development testing has shown that ionic silver in aqueous solution was maintained at essentially the same level of addition (0.4 ppm) for up to 15 months with method (5) (a combination of methods (1) and (2)), before the test was discontinued for nickel-based alloys. Method (1) resulted in the maintenance of a biocidal level (approximately 0.05 ppm) for up to 10 months before that test was discontinued for nickel-based alloys. Methods (1) and (2) used separately were able to maintain ionic silver in aqueous solution at essentially the same level of addition (0.4 ppm) for up to 10 months before the test was discontinued for stainless steel alloys. Method (3) was only utilized for titanium alloys, and was successful at maintaining ionic silver in aqueous solution at

  17. Special Issue: Coinage Metal (Copper, Silver, and Gold) Catalysis.

    PubMed

    Carabineiro, Sónia Alexandra Correia

    2016-01-01

    The subject of catalysis by coinage metals (copper, silver, and gold) comes up increasingly day-by-day. This Special Issue aims to cover the numerous aspects of the use of these metals as catalysts for several reactions. It deals with synthesis and characterization of copper, silver and gold based catalysis, their characterization and use, both for heterogeneous and homogeneous catalysis, and some of their potential applications. PMID:27338316

  18. Advanced mercury removal from gold leachate solutions prior to gold and silver extraction: a field study from an active gold mine in Peru.

    PubMed

    Matlock, Matthew M; Howerton, Brock S; Van Aelstyn, Mike A; Nordstrom, Fredrik L; Atwood, David A

    2002-04-01

    Mercury contamination in the Gold-Cyanide Process (GCP) is a serious health and environmental problem. Following the heap leaching of gold and silver ores with NaCN solutions, portions of the mercury-cyano complexes often adhere to the activated carbon (AC) used to extract the gold. During the electrowinning and retorting steps, mercury can be (and often is) emitted to the air as a vapor. This poses a severe health hazard to plant workers and the local environment. Additional concerns relate to the safety of workers when handling the mercury-laden AC. Currently, mercury treatment from the heap leach solution is nonexistent. This is due to the fact that chelating ligands which can effectively work under the adverse pH conditions (as present in the heap leachate solutions) do not exist. In an effort to economically and effectively treat the leachate solution prior to passing over the AC, a dipotassium salt of 1,3-benzenediamidoethanethiol (BDET2-) has been developed to irreversibly bind and precipitate the mercury. The ligand has proven to be highly effective by selectively reducing mercury levels from average initial concentrations of 34.5 ppm (parts per million) to 0.014 ppm within 10 min and to 0.008 ppm within 15 min. X-ray powder diffraction (XRD), proton nuclear magnetic resonance (1H NMR), Raman, and infrared (IR) spectroscopy demonstrate the formation of a mercury-ligand compound, which remains insoluble over pH ranges of 0.0-14.0. Leachate samples from an active gold mine in Peru have been analyzed using cold vapor atomic fluorescence (CVAF) and inductively coupled plasma optical emission spectroscopy (ICP-OES) for metal concentrations before and after treatment with the BDET2- ligand. PMID:11999077

  19. Method for extracting copper, silver and related metals

    DOEpatents

    Moyer, Bruce A.; McDowell, W. J.

    1990-01-01

    A process for selectively extracting precious metals such as silver and gold concurrent with copper extraction from aqueous solutions containing the same. The process utilizes tetrathiamacrocycles and high molecular weight organic acids that exhibit a synergistic relationship when complexing with certain metal ions thereby removing them from ore leach solutions.

  20. Method for extracting copper, silver and related metals

    DOEpatents

    Moyer, B.A.; McDowell, W.J.

    1987-10-23

    A process for selectively extracting precious metals such as silver and gold concurrent with copper extraction from aqueous solutions containing the same. The process utilizes tetrathiamacrocycles and high molecular weight organic acids that exhibit a synergistic relationship when complexing with certain metal ions thereby removing them from ore leach solutions.

  1. Method for extracting copper, silver and related metals

    SciTech Connect

    Moyer, B.A.; McDowell, W.J.

    1990-05-22

    This patent describes a process for selectively extracting precious metal such as silver and gold concurrent with copper extraction from aqueous solutions containing the same. The process utilizes tetrathiamacrocycles and high molecular weight organic acids that exhibit a synergistic relationship when complexing with certain metal ions thereby removing them from ore leach solutions.

  2. Mercury localization in mouse kidney over time: autoradiography versus silver staining

    SciTech Connect

    Rodier, P.M.; Kates, B.; Simons, R.

    1988-02-01

    Several methods of silver staining have been employed to localize mercury in tissue, under the assumption that the techniques represent total Hg, but recent reports have suggested that these stains are specific for a limited fraction of the Hg present in some samples. Magos et al. hypothesized that the stains actually vary with inorganic mercury content. The purpose of the present study was to compare localization by radiolabeling to localization by one silver stain, the photoemulsion histochemical technique, in tissues prepared to contain a range of levels of total Hg and a range of levels of inorganic Hg. Mice dosed with 8 mg Hg/kg as MeHg were killed 24 hr, 1 week, or 2 weeks after exposure, to allow a decrease in total Hg and an increase in the proportion of demethylated Hg over time. Mice dosed with 4 mg Hg/kg as HgCl/sub 2/ provided samples in which all the Hg present was in the inorganic form. Atomic absorption of kidneys of mice dosed with MeHg showed that total Hg fell from 55 micrograms/g to 39 to 25 over 2 weeks, while the inorganic fraction climbed from about 2 to 27 to 35%. Grain counts from autoradiographs of /sup 203/Hg-labeled sections correlated with total Hg content at +0.88, but silver staining was correlated with inorganic Hg content, appearing only at late termination times in MeHg-exposed animals, but soon after dosing in mice exposed to inorganic Hg. The photoemulsion histochemical technique revealed a substance strictly localized in the proximal tubules, while autoradiographs and grain counts showed total Hg to be present throughout the kidney tissue. These results support the contention that silver stains are selective for inorganic Hg.

  3. Synthetic silver oxide and mercury-free zinc electrodes for silver-zinc reserve batteries

    NASA Astrophysics Data System (ADS)

    Smith, David F.; Gucinski, James A.

    Reserve activated silver oxide-zinc cells were constructed with synthetic silver oxide (Ag 2O) electrodes with Pb-treated zinc electrodes produced by a non-electrolytic process. The cells were tested before and after thermally accelerated aging. At discharge rates up to 80 mA cm -2, the discharge was limited by the Ag 2O electrode, with a coulombic efficiency between 89-99%. At higher rates, the cells are apparently zinc-limited. Test cells were artificially aged at 90°C for 19 h and discharged at 21°C at 80 mA cm -2. No capacity loss was measured, but a delayed activation rise time was noted (192 ms fresh vs. 567 ms aged). The delay is thought to be caused by zinc passivation due to the outgassing of cell materials.

  4. 40 CFR 421.250 - Applicability: Description of the primary precious metals and mercury subcategory.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... primary precious metals and mercury subcategory. 421.250 Section 421.250 Protection of Environment... POINT SOURCE CATEGORY Primary Precious Metals and Mercury Subcategory § 421.250 Applicability: Description of the primary precious metals and mercury subcategory. The provisions of this subpart...

  5. 40 CFR 421.250 - Applicability: Description of the primary precious metals and mercury subcategory.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... primary precious metals and mercury subcategory. 421.250 Section 421.250 Protection of Environment... POINT SOURCE CATEGORY Primary Precious Metals and Mercury Subcategory § 421.250 Applicability: Description of the primary precious metals and mercury subcategory. The provisions of this subpart...

  6. 40 CFR 421.250 - Applicability: Description of the primary precious metals and mercury subcategory.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... primary precious metals and mercury subcategory. 421.250 Section 421.250 Protection of Environment... POINT SOURCE CATEGORY Primary Precious Metals and Mercury Subcategory § 421.250 Applicability: Description of the primary precious metals and mercury subcategory. The provisions of this subpart...

  7. 40 CFR 421.250 - Applicability: Description of the primary precious metals and mercury subcategory.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... POINT SOURCE CATEGORY Primary Precious Metals and Mercury Subcategory § 421.250 Applicability: Description of the primary precious metals and mercury subcategory. The provisions of this subpart are... primary precious metals and mercury subcategory. 421.250 Section 421.250 Protection of...

  8. 40 CFR 421.250 - Applicability: Description of the primary precious metals and mercury subcategory.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... POINT SOURCE CATEGORY Primary Precious Metals and Mercury Subcategory § 421.250 Applicability: Description of the primary precious metals and mercury subcategory. The provisions of this subpart are... primary precious metals and mercury subcategory. 421.250 Section 421.250 Protection of...

  9. Determination of copper, nickel, cobalt, silver, lead, cadmium, and mercury ions in water by solid-phase extraction and the RP-HPLC with UV-Vis detection.

    PubMed

    Hu, Qiufen; Yang, Guangyu; Zhao, Yiyun; Yin, Jiayuan

    2003-03-01

    A new method for the simultaneous determination of seven heavy metal ions in water by solid-phase extraction and reversed-phase high-performance liquid chromatography (RP-HPLC) was developed. The copper, nickel, cobalt, silver, lead, cadmium, and mercury ions were pre-column derivatized with tetra( m-aminophenyl)porphyrin (T m-APP) to form colored chelates. The metal-T m-APP chelates in 100 mL of sample were preconcentrated to 1 mL by solid-phase extraction with a C(18 )cartridge; an enrichment factor of 100 was achieved. The chelates were separated on a Waters Xterra()RP(18) column by gradient elution with methanol (containing 0.05 mol L(-1) pyrrolidine-acetic acid buffer salt, pH 10.0) and acetone (containing 0.05 mol L(-1) pyrrolidine-acetic acid buffer salt, pH 10.0) as mobile phase at a flow rate of 1.0 mL min(-1) and detected with a photodiode array detector. The detection limits of copper, cobalt, nickel, silver, lead, cadmium, and mercury are 2, 2, 3, 4, 3, 3, and 3 ng L(-1), respectively, in the original sample. The method was also applied to the determination of these metals in water with good results. PMID:12664186

  10. Mercury

    NASA Astrophysics Data System (ADS)

    Taylor, G. J.; Scott, E. R. D.

    2003-12-01

    Mercury is an important part of the solar system puzzle, yet we know less about it than any other planet, except Pluto. Mercury is the smallest of the terrestrial planets (0.05 Earth masses) and the closest to the Sun. Its relatively high density (5.4 g cm -3) indicates that it has a large metallic core (˜3/4 of the planet's radius) compared to its silicate mantle and crust. The existence of a magnetic field implies that the metallic core is still partly molten. The surface is heavily cratered like the highlands of the Moon, but some areas are smooth and less cratered, possibly like the lunar maria (but not as dark). Its surface composition, as explained in the next section, appears to be low in FeO (only ˜3 wt.%), which implies that either its crust is anorthositic (Jeanloz et al., 1995) or its mantle is similarly low in FeO ( Robinson and Taylor, 2001).The proximity of Mercury to the Sun is particularly important. In one somewhat outmoded view of how the solar system formed, Mercury was assembled in the hottest region close to the Sun so that virtually all of the iron was in the metallic state, rather than oxidized to FeO (e.g., Lewis, 1972, 1974). If correct, Mercury ought to have relatively a low content of FeO. This hypothesis also predicts that Mercury should have high concentrations of refractory elements, such as calcium, aluminum, and thorium, and low concentrations of volatile elements, such as sodium and potassium, compared to the other terrestrial planets.Alternative hypotheses tell a much more nomadic and dramatic story of Mercury's birth. In one alternative view, wandering planetesimals that might have come from as far away as Mars or the inner asteroid belt accreted to form Mercury (Wetherill, 1994). This model predicts higher FeO and volatile elements than does the high-temperature model, and similar compositions among the terrestrial planets. The accretion process might have been accompanied by a monumental impact that stripped away much of the

  11. Quantification of metal loading to Silver Creek through the Silver Maple Claims area, Park City, Utah, May 2002

    USGS Publications Warehouse

    Kimball, Briant A.; Johnson, Kevin K.; Runkel, Robert L.; Steiger, Judy I.

    2004-01-01

    The Silver Maple Claims area along Silver Creek, near Park City, Utah, is administered by the Bureau of Land Management. To quantify possible sources of elevated zinc concentrations in Silver Creek that exceed water-quality standards, the U.S. Geological Survey conducted a mass-loading study in May 2002 along a 1,400-meter reach of Silver Creek that included the Silver Maple Claims area. Additional samples were collected upstream and downstream from the injection reach to investigate other possible sources of zinc and other metals to the stream. Many metals were investigated in the study, but zinc is of particular concern for water-quality standards. The total loading of zinc along the study reach from Park City to Wanship, Utah, was about 49 kilograms per day. The Silver Maple Claims area contributed about 38 percent of this load. The Silver Creek tailings discharge pipe, which empties just inside the Silver Maple Claims area, contributed more than half the load of the Silver Maple Claims area. Substantial zinc loads also were added to Silver Creek downstream from the Silver Maple Claims area. Ground-water discharge upstream from the waste-water treatment plant contributed 20 percent of the total zinc load, and another 17 percent was contributed near the waste-water treatment plant. By identifying the specific areas where zinc and other metal loads are contributed to Silver Creek, it is possible to assess the needs of a remediation plan. For example, removing the tailings from the Silver Maple Claims area could contribute to lowering the zinc concentration in Silver Creek, but without also addressing the loading from the Silver Creek tailings discharge pipe and the ground-water discharge farther downstream, the zinc concentration could not be lowered enough to meet water-quality standards. Additional existing sources of zinc loading downstream from the Silver Maple Claims area could complicate the process of lowering zinc concentration to meet water

  12. Public health response to metallic mercury spills in Kansas.

    PubMed

    Monroe, C T; Pezzino, G; Knoche, L L; Henning, L; Belt, P

    1999-11-01

    Local and state public health officials are called on to respond to environmental public health hazards just as they historically have been called on to respond to communicable disease outbreaks. Recent experience with metallic mercury spills in Kansas suggests that neither the legal authority nor the scientific knowledgebase is as well developed for response to environmental hazards as for communicable disease threats. PMID:10662059

  13. Estimating historical atmospheric mercury concentrations from silver mining and their legacies in present-day surface soil in Potosí, Bolivia

    NASA Astrophysics Data System (ADS)

    Hagan, Nicole; Robins, Nicholas; Hsu-Kim, Heileen; Halabi, Susan; Morris, Mark; Woodall, George; Zhang, Tong; Bacon, Allan; Richter, Daniel De B.; Vandenberg, John

    2011-12-01

    Detailed Spanish records of mercury use and silver production during the colonial period in Potosí, Bolivia were evaluated to estimate atmospheric emissions of mercury from silver smelting. Mercury was used in the silver production process in Potosí and nearly 32,000 metric tons of mercury were released to the environment. AERMOD was used in combination with the estimated emissions to approximate historical air concentrations of mercury from colonial mining operations during 1715, a year of relatively low silver production. Source characteristics were selected from archival documents, colonial maps and images of silver smelters in Potosí and a base case of input parameters was selected. Input parameters were varied to understand the sensitivity of the model to each parameter. Modeled maximum 1-h concentrations were most sensitive to stack height and diameter, whereas an index of community exposure was relatively insensitive to uncertainty in input parameters. Modeled 1-h and long-term concentrations were compared to inhalation reference values for elemental mercury vapor. Estimated 1-h maximum concentrations within 500 m of the silver smelters consistently exceeded present-day occupational inhalation reference values. Additionally, the entire community was estimated to have been exposed to levels of mercury vapor that exceed present-day acute inhalation reference values for the general public. Estimated long-term maximum concentrations of mercury were predicted to substantially exceed the EPA Reference Concentration for areas within 600 m of the silver smelters. A concentration gradient predicted by AERMOD was used to select soil sampling locations along transects in Potosí. Total mercury in soils ranged from 0.105 to 155 mg kg-1, among the highest levels reported for surface soils in the scientific literature. The correlation between estimated air concentrations and measured soil concentrations will guide future research to determine the extent to which the

  14. Advanced Gasification Mercury/Trace Metal Control with Monolith Traps

    SciTech Connect

    Musich, Mark; Swanson, Michael; Dunham, Grant; Stanislowski, Joshua

    2010-10-05

    Two Corning monoliths and a non-carbon-based material have been identified as potential additives for mercury capture in syngas at temperatures above 400°F and pressure of 600 psig. A new Corning monolith formulation, GR-F1-2189, described as an active sample appeared to be the best monolith tested to date. The Corning SR Liquid monolith concept continues to be a strong candidate for mercury capture. Both monolith types allowed mercury reduction to below 5-μg/m{sup 3} (~5 ppb), a current U.S. Department of Energy (DOE) goal for trace metal control. Preparation methods for formulating the SR Liquid monolith impacted the ability of the monolith to capture mercury. The Energy & Environmental Research Center (EERC)-prepared Noncarbon Sorbents 1 and 2 appeared to offer potential for sustained and significant reduction of mercury concentration in the simulated fuel gas. The Noncarbon Sorbent 1 allowed sustained mercury reduction to below 5-μg/m{sup 3} (~5 ppb). The non-carbon-based sorbent appeared to offer the potential for regeneration, that is, desorption of mercury by temperature swing (using nitrogen and steam at temperatures above where adsorption takes place). A Corning cordierite monolith treated with a Group IB metal offered limited potential as a mercury sorbent. However, a Corning carbon-based monolith containing prereduced metallic species similar to those found on the noncarbon sorbents did not exhibit significant or sustained mercury reduction. EERC sorbents prepared with Group IB and IIB selenide appeared to have some promise for mercury capture. Unfortunately, these sorbents also released Se, as was evidenced by the measurement of H2Se in the effluent gas. All sorbents tested with arsine or hydrogen selenide, including Corning monoliths and the Group IB and IIB metal-based materials, showed an ability to capture arsine or hydrogen selenide at 400°F and 600 psig. Based on current testing, the noncarbon metal-based sorbents appear to be the most

  15. ADVANCED GASIFICATION MERCURY/TRACE METAL CONTROL WITH MONOLITH TRAPS

    SciTech Connect

    Mark A. Musich; Michael L. Swanson; Grant E. Dunham; Joshua J. Stanislowski

    2010-07-31

    Two Corning monoliths and a non-carbon-based material have been identified as potential additives for mercury capture in syngas at temperatures above 400°F and pressure of 600 psig. A new Corning monolith formulation, GR-F1-2189, described as an active sample appeared to be the best monolith tested to date. The Corning SR Liquid monolith concept continues to be a strong candidate for mercury capture. Both monolith types allowed mercury reduction to below 5-μg/m3 (~5 ppb), a current U.S. Department of Energy (DOE) goal for trace metal control. Preparation methods for formulating the SR Liquid monolith impacted the ability of the monolith to capture mercury. The Energy & Environmental Research Center (EERC)-prepared Noncarbon Sorbents 1 and 2 appeared to offer potential for sustained and significant reduction of mercury concentration in the simulated fuel gas. The Noncarbon Sorbent 1 allowed sustained mercury reduction to below 5-μg/m3 (~5 ppb). The non-carbon-based sorbent appeared to offer the potential for regeneration, that is, desorption of mercury by temperature swing (using nitrogen and steam at temperatures above where adsorption takes place). A Corning cordierite monolith treated with a Group IB metal offered limited potential as a mercury sorbent. However, a Corning carbon-based monolith containing prereduced metallic species similar to those found on the noncarbon sorbents did not exhibit significant or sustained mercury reduction. EERC sorbents prepared with Group IB and IIB selenide appeared to have some promise for mercury capture. Unfortunately, these sorbents also released Se, as was evidenced by the measurement of H2Se in the effluent gas. All sorbents tested with arsine or hydrogen selenide, including Corning monoliths and the Group IB and IIB metal-based materials, showed an ability to capture arsine or hydrogen selenide at 400°F and 600 psig. Based on current testing, the noncarbon metal-based sorbents appear to be the most effective arsine

  16. 41 CFR 109-45.1003 - Recovery of silver from precious metals bearing materials.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 41 Public Contracts and Property Management 3 2013-07-01 2013-07-01 false Recovery of silver from... of Precious Metals § 109-45.1003 Recovery of silver from precious metals bearing materials. The... establishment and maintenance of a program for silver recovery from used hypo solution and scrap film....

  17. 41 CFR 109-45.1003 - Recovery of silver from precious metals bearing materials.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 41 Public Contracts and Property Management 3 2012-01-01 2012-01-01 false Recovery of silver from... of Precious Metals § 109-45.1003 Recovery of silver from precious metals bearing materials. The... establishment and maintenance of a program for silver recovery from used hypo solution and scrap film....

  18. 41 CFR 109-45.1003 - Recovery of silver from precious metals bearing materials.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 41 Public Contracts and Property Management 3 2010-07-01 2010-07-01 false Recovery of silver from... of Precious Metals § 109-45.1003 Recovery of silver from precious metals bearing materials. The... establishment and maintenance of a program for silver recovery from used hypo solution and scrap film....

  19. 41 CFR 109-45.1003 - Recovery of silver from precious metals bearing materials.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 41 Public Contracts and Property Management 3 2011-01-01 2011-01-01 false Recovery of silver from... of Precious Metals § 109-45.1003 Recovery of silver from precious metals bearing materials. The... establishment and maintenance of a program for silver recovery from used hypo solution and scrap film....

  20. 41 CFR 109-45.1003 - Recovery of silver from precious metals bearing materials.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 41 Public Contracts and Property Management 3 2014-01-01 2014-01-01 false Recovery of silver from... of Precious Metals § 109-45.1003 Recovery of silver from precious metals bearing materials. The... establishment and maintenance of a program for silver recovery from used hypo solution and scrap film....

  1. Fabrication of carbon, gold, platinum, silver, and mercury ultramicroelectrodes with controlled geometry.

    PubMed

    Danis, Laurence; Polcari, David; Kwan, Annie; Gateman, Samantha Michelle; Mauzeroll, Janine

    2015-03-01

    A simple, fast, and reproducible method for the fabrication of disk ultramicroelectrodes (UMEs) with controlled geometry is reported. The use of prepulled soda-lime glass capillaries allows one to bypass the irreproducible torch-sealing and experimentally challenging tip-sharpening steps used in conventional fabrication protocols. A micron-sized electroactive wire is sealed inside this capillary producing UMEs with a highly reproducible geometry. Total fabrication time (1 h) and experimental difficulty are significantly reduced. Disk UMEs with various diameters and cores were fabricated, including carbon fiber (7 and 11 μm), gold (10 and 25 μm), platinum (10 and 25 μm), silver (25 μm), and mercury (25 μm). The ratio of the insulating sheath to the electroactive core of the UMEs was 2.5-3.6. Silver UMEs were also used to produce a Ag/AgCl microreference electrode. This general fabrication method can readily be applied to other electroactive cores and could allow any research group to produce high quality disk UMEs, which are a prerequisite for quantitative scanning electrochemical microscopy. PMID:25629426

  2. Sunlight mediated synthesis of silver nanoparticles using redox phytoprotein and their application in catalysis and colorimetric mercury sensing.

    PubMed

    Ahmed, Khan Behlol Ayaz; Senthilnathan, Rajendran; Megarajan, Sengan; Anbazhagan, Veerappan

    2015-10-01

    Owing to the benign nature, plant extracts mediated green synthesis of metal nanoparticles (NPs) is rapidly expanding. In this study, we demonstrated the successful green synthesis of silver nanoparticles (AgNPs) by utilizing natural sunlight and redox protein complex composed of ferredoxin-NADP(+) reductase (FNR) and ferredoxin (FD). The capping and stabilization of the AgNPs by the redox protein was confirmed by Fourier transform infrared spectroscopy. Light and redox protein is the prerequisite factor for the formation of AgNPs. The obtained result shows that the photo generated free radicals by the redox protein is responsible for the reduction of Ag(+) to Ag(0). Transmission electron microscopy revealed the formation of spherical AgNPs with size ranging from 10 to 15 nm. As-prepared AgNPs exhibit excellent catalytic activity toward the degradation of hazardous organic dyes, such as methylene blue, methyl orange and methyl red. These bio-inspired AgNPs is highly sensitive and selective in sensing hazardous mercury ions in the water at micromolar concentration. In addition, FNR/FD extract stabilized AgNPs showed good antimicrobial activity against gram positive and gram negative bacteria. PMID:26163946

  3. High-throughput colorimetric assays for mercury(II) in blood and wastewater based on the mercury-stimulated catalytic activity of small silver nanoparticles in a temperature-switchable gelatin matrix.

    PubMed

    Sun, Zongzhao; Zhang, Ning; Si, Yanmei; Li, Shuai; Wen, Jiangwei; Zhu, Xiangbing; Wang, Hua

    2014-08-21

    A catalysis-based, label-free, and high-throughput colorimetric protocol has been initially proposed for detecting mercury(II) in blood and wastewater with 96-cell plates, based on the mercury-enhanced catalytic activity of small silver nanoparticles synthesized in a gelatin matrix with unique temperature switchable sol-gel transition. PMID:24995435

  4. Mercury and Your Health

    MedlinePlus

    ... the Risk of Exposure to Mercury Learn About Mercury What is Mercury What is Metallic mercury? Toxicological Profile ToxFAQs Mercury Resources CDC’s National Biomonitoring Program Factsheet on Mercury ...

  5. Effect of mercury-silver alloy composition on the open-circuit voltage of cadmium/mercuric oxide cells

    SciTech Connect

    Kronenberg, M.L.; Stein, B.J.; Codd, B.P. )

    1994-10-01

    To minimize the migration of mercury droplets when discharging cadmium/mercuric oxide (Cd/HgO) cells, silver powder is often blended with HgO powder in the cathode to promote formation of a solid Hg-Ag alloy. Even though only high purity materials are used, open-circuit cell voltages are much higher than what is normally observed when Ag powder is not present. There is also a significant variation in the open-circuit voltage (OCV) of a given lot of Cd/HgO cells. The authors hypothesized that this high OCV and cell voltage variation is at least partially attributed to uncontrolled very small quantities of mercury present in the HgO. The potential variations arise from the reduced activity of mercury in the Hg-Ag alloy. The experiments that were carried out and reported here support this hypothesis.

  6. Metal-induced fluorescence properties of three-dimensionally ordered macroporous silver inverse opal platforms

    NASA Astrophysics Data System (ADS)

    Chae, Weon-Sik; Lee, Myung-Jin; Kim, Kisun; Hyun, Jerome K.; Jeon, Seokwoo

    2016-02-01

    This study examined the metal-induced fluorescence properties of three-dimensionally ordered macroporous silver inverse opal (IO) films. Electrochemically synthesized silver IO films with a micrometer cavity exhibited notable fluorescence enhancement at the silver frame, and a decrease in fluorescence lifetime. Numerical calculations supported the observations of a higher fluorescence efficiency at the frame than in the cavity.

  7. Solid phase extraction of trace amounts of silver, cadmium, copper, mercury, and lead in various food samples based on ethylene glycol bis-mercaptoacetate modified 3-(trimethoxysilyl)-1-propanethiol coated Fe3O4 nanoparticles.

    PubMed

    Mashhadizadeh, Mohammad Hossein; Amoli-Diva, Mitra; Shapouri, Mahmoud Reza; Afruzi, Hossein

    2014-05-15

    Extraction, pre-concentration, and determination of trace amounts of silver, cadmium, copper, mercury, and lead from some food samples were investigated by magnetic solid phase extraction using Fe3O4 nanoparticles coated with 3-(trimethoxysilyl)-1-propanethiol and modified with ethylene glycol bis-mercaptoacetate as a new adsorbent. SEM, X-ray diffraction, and FT-IR were used to characterise the adsorbent. Metal ions were measured using ICP-OES, except for mercury, which was determined by CV-AAS method. Various factors affecting the extraction and desorption of target metal ions were investigated. 1 mL of 1 mol/L HCl and 5% thiourea was used as eluent. The detection limits of 0.07, 0.06, 0.09, 0.01, and 0.08 ng/mL were obtained for silver, cadmium, copper, mercury, and lead with enrichment factors of 240, 294, 297, 291, and 236, respectively. The method was used for determination of target metal ions in rice, canned tuna fish, and tea leaves. PMID:24423536

  8. Silver metal colloidal film on a flexible polymer substrate

    NASA Astrophysics Data System (ADS)

    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).

  9. Oil-Soluble Silver-Organic Molecule for in Situ Deposition of Lubricious Metallic Silver at High Temperatures.

    PubMed

    Desanker, Michael; Johnson, Blake; Seyam, Afif M; Chung, Yip-Wah; Bazzi, Hassan S; Delferro, Massimiliano; Marks, Tobin J; Wang, Q Jane

    2016-06-01

    A major challenge in lubrication technology is to enhance lubricant performance at extreme temperatures that exceed conventional engine oil thermal degradation limits. Soft noble metals such as silver have low reactivity and shear strength, which make them ideal solid lubricants for wear protection and friction reduction between contacting surfaces at high temperatures. However, achieving adequate dispersion in engine lubricants and metallic silver deposition over predetermined temperatures ranges presents a significant chemical challenge. Here we report the synthesis, characterization, and tribological implementation of the trimeric silver pyrazolate complex, [Ag(3,5-dimethyl-4-n-hexyl-pyrazolate)]3 (1). This complex is oil-soluble and undergoes clean thermolysis at ∼310 °C to deposit lubricious, protective metallic silver particles on metal/metal oxide surfaces. Temperature-controlled tribometer tests show that greater than 1 wt % loading of 1 reduces wear by 60% in PAO4, a poly-α-olefin lubricant base fluid, and by 70% in a commercial fully formulated 15W40 motor oil (FF oil). This silver-organic complex also imparts sufficient friction reduction so that the tribological transition from oil as the primary lubricant through its thermal degradation, to 1 as the primary lubricant, is experimentally undetectable. PMID:27163783

  10. Packaging a liquid metal ESD with micro-scale Mercury droplet.

    SciTech Connect

    Barnard, Casey Anderson

    2011-08-01

    A liquid metal ESD is being developed to provide electrical switching at different acceleration levels. The metal will act as both proof mass and electric contact. Mercury is chosen to comply with operation parameters. There are many challenges surrounding the deposition and containment of micro scale mercury droplets. Novel methods of micro liquid transfer are developed to deliver controllable amounts of mercury to the appropriate channels in volumes under 1 uL. Issues of hermetic sealing and avoidance of mercury contamination are also addressed.

  11. Mercury

    MedlinePlus

    ... button batteries. Mercury salts may be used in skin creams and ointments. It's also used in many industries. Mercury in the air settles into water. It can pass through the food chain and build up in ...

  12. Metal-Enhanced Fluorescence of Silver Island Associated with Silver Nanoparticle.

    PubMed

    Liaw, Jiunn-Woei; Wu, Hsin-Yu; Huang, Chu-Chuan; Kuo, Mao-Kuen

    2016-12-01

    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 higher than that of a SNP or a SI alone due to the coupled gap mode. This finding is in agreement with the previous experimental results. In addition, the plasmon band of the structure is broadband and tunable, which can be red-shifted and broadened by flattening or enlarging SI. Based on this property, the hybrid nanostructure can be tailored to obtain the optimal enhancement factor on a specific molecule according to its excitation spectrum. Moreover, we found that there is an induced optical force allowing SNP be attracted by SI. Consequently, the gap is reduced gradually to perform a stronger MEF effect. PMID:26779917

  13. Metal-Enhanced Fluorescence of Silver Island Associated with Silver Nanoparticle

    NASA Astrophysics Data System (ADS)

    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 higher than that of a SNP or a SI alone due to the coupled gap mode. This finding is in agreement with the previous experimental results. In addition, the plasmon band of the structure is broadband and tunable, which can be red-shifted and broadened by flattening or enlarging SI. Based on this property, the hybrid nanostructure can be tailored to obtain the optimal enhancement factor on a specific molecule according to its excitation spectrum. Moreover, we found that there is an induced optical force allowing SNP be attracted by SI. Consequently, the gap is reduced gradually to perform a stronger MEF effect.

  14. Mercury heavy-metal-induced physiochemical changes and genotoxic alterations in water hyacinths [Eichhornia crassipes (Mart.)].

    PubMed

    Malar, Srinivasan; Sahi, Shivendra Vikram; Favas, Paulo J C; Venkatachalam, Perumal

    2015-03-01

    Mercury heavy metal pollution has become an important environmental problem worldwide. Accumulation of mercury ions by plants may disrupt many cellular functions and block normal growth and development. To assess mercury heavy metal toxicity, we performed an experiment focusing on the responses of Eichhornia crassipes to mercury-induced oxidative stress. E. crassipes seedlings were exposed to varying concentrations of mercury to investigate the level of mercury ions accumulation, changes in growth patterns, antioxidant defense mechanisms, and DNA damage under hydroponics system. Results showed that plant growth rate was significantly inhibited (52 %) at 50 mg/L treatment. Accumulation of mercury ion level were 1.99 mg/g dry weight, 1.74 mg/g dry weight, and 1.39 mg/g dry weight in root, leaf, and petiole tissues, respectively. There was a decreasing trend for chlorophyll a, b, and carotenoids with increasing the concentration of mercury ions. Both the ascorbate peroxidase and malondialdehyde contents showed increased trend in leaves and roots up to 30 mg/L mercury treatment and slightly decreased at the higher concentrations. There was a positive correlation between heavy metal dose and superoxide dismutase, catalase, and peroxidase antioxidative enzyme activities which could be used as biomarkers to monitor pollution in E. crassipes. Due to heavy metal stress, some of the normal DNA bands were disappeared and additional bands were amplified compared to the control in the random amplified polymorphic DNA (RAPD) profile. Random amplified polymorphic DNA results indicated that genomic template stability was significantly affected by mercury heavy metal treatment. We concluded that DNA changes determined by random amplified polymorphic DNA assay evolved a useful molecular marker for detection of genotoxic effects of mercury heavy metal contamination in plant species. PMID:25323404

  15. Reversible transformations of silver oxide and metallic silver nanoparticles inside SiO{sub 2} films

    SciTech Connect

    Pal, Sudipto; De, Goutam

    2009-02-04

    Reversible transformation of silver oxide and metallic nanoparticles inside a relatively porous silica film has been established. Annealing of Ag-doped films in oxidizing (air) atmosphere at 450 deg. C yielded colorless films containing AgO{sub x}. These films were turned yellow when heated in H{sub 2}-N{sub 2} (reducing atmosphere) due to the formation of Ag nanoparticles. This yellow coloration (due to nano Ag{sup 0}) and bleaching (conversion of Ag{sup 0} {yields} Ag{sup +}) are reversible. Optical and photoluminescence spectra are well consistent with this coloration and bleaching. The soaking test of the air-annealed film in Na{sub 2}S{sub 2}O{sub 3} solution supports the presence of Ag{sup +}. Grazing incidence X-ray diffraction and transmission electron microscopy studies reveal the formation of Ag-oxides and Ag nanoparticles in the oxidized and reduced films, respectively.

  16. Advanced Gasification Mercury/Trace Metal Control with Monolith Traps

    SciTech Connect

    Michael L. Swanson; Grant E. Dunham; Mark A. Musich

    2007-02-01

    Three potential additives for controlling mercury emissions from syngas at temperatures ranging from 350 to 500 F (177 to 260 C) were developed. Current efforts are being directed at increasing the effective working temperature for these sorbents and also being able to either eliminate any potential mercury desorption or trying to engineer a trace metal removal system that can utilize the observed desorption process to repeatedly regenerate the same sorbent monolith for extended use. Project results also indicate that one of these same sorbents can also successfully be utilized for arsenic removal. Capture of the hydrogen selenide in the passivated tubing at elevated temperatures has resulted in limited results on the effective control of hydrogen selenide with these current sorbents, although lower-temperature results are promising. Preliminary economic analysis suggests that these Corning monoliths potentially could be more cost-effective than the conventional cold-gas (presulfided activated carbon beds) technology currently being utilized. Recent Hg-loading results might suggest that the annualized costs might be as high as 2.5 times the cost of the conventional technology. However, this annualized cost does not take into account the significantly improved thermal efficiency of any plant utilizing the warm-gas monolith technology currently being developed.

  17. MERCURY CONTRIBUTIONS TO THE ENVIRONMENT FROM HISTORIC MINING PRACTICES

    EPA Science Inventory

    Significant quantities of mercury have been released to the environment as a result of historic precious metal mining. Many gold and silver deposits are enriched in mercury, which is released during mining and processing activities. Historically in the U.S., although a modern ...

  18. INKJET PRINTING OF NICKEL AND SILVER METAL SOLAR CELL CONTACTS

    SciTech Connect

    Pasquarelli, R.; Curtis, C.; Van Hest, M.

    2008-01-01

    With about 125,000 terawatts of solar power striking the earth at any given moment, solar energy may be the only renewable energy resource with enough capacity to meet a major portion of our future energy needs. Thin-fi lm technologies and solution deposition processes seek to reduce manufacturing costs in order to compete with conventional coal-based electricity. Inkjet printing, as a derivative of the direct-write process, offers the potential for low-cost, material-effi cient deposition of the metals for photovoltaic contacts. Advances in contact metallizations are important because they can be employed on existing silicon technology and in future-generation devices. We report on the atmospheric, non-contact deposition of nickel (Ni) and silver (Ag) metal patterns on glass, Si, and ZnO substrates at 180–220°C from metal-organic precursor inks using a Dimatix inkjet printer. Near-bulk conductivity Ag contacts were successfully printed up to 4.5 μm thick and 130 μm wide on the silicon nitride antirefl ective coating of silicon solar cells. Thin, high-resolution Ni adhesion-layer lines were printed on glass and zinc oxide at 80 μm wide and 55 nm thick with a conductivity two orders of magnitude less than the bulk metal. Additionally, the ability to print multi-layered metallizations (Ag on Ni) on transparent conducting oxides was demonstrated and is promising for contacts in copper-indium-diselenide (CIS) solar cells. Future work will focus on further improving resolution, printing full contact devices, and investigating copper inks as a low-cost replacement for Ag contacts.

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

    PubMed

    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

  20. Ionic polymer metal composites with polypyrrole-silver electrodes

    NASA Astrophysics Data System (ADS)

    Cellini, F.; Grillo, A.; Porfiri, M.

    2015-03-01

    Ionic polymer metal composites (IPMCs) are a class of soft active materials that are finding increasing application in robotics, environmental sensing, and energy harvesting. In this letter, we demonstrate the fabrication of IPMCs via in-situ photoinduced polymerization of polypyrrole-silver electrodes on an ionomeric membrane. The composition, morphology, and sheet resistance of the electrodes are extensively characterized through a range of experimental techniques. We experimentally investigate IPMC electrochemistry through electrochemical impedance spectroscopy, and we propose a modified Randle's model to interpret the impedance spectrum. Finally, we demonstrate in-air dynamic actuation and sensing and assess IPMC performance against more established fabrication methods. Given the simplicity of the process and the short time required for the formation of the electrodes, we envision the application of our technique in the development of a rapid prototyping technology for IPMCs.

  1. 40 CFR 266.106 - Standards to control metals emissions.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... height (Ha) may not exceed good engineering practice as specified in 40 CFR 51.100(ii). (iii) If the TESH...) Noncarcinogenic metals. The feed rates of antimony, barium, lead, mercury, thallium, and silver in all feed..., barium, mercury, thallium, and silver are based on either: (A) An hourly rolling average as defined...

  2. 40 CFR 266.106 - Standards to control metals emissions.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... height (Ha) may not exceed good engineering practice as specified in 40 CFR 51.100(ii). (iii) If the TESH...) Noncarcinogenic metals. The feed rates of antimony, barium, lead, mercury, thallium, and silver in all feed..., barium, mercury, thallium, and silver are based on either: (A) An hourly rolling average as defined...

  3. 40 CFR 266.106 - Standards to control metals emissions.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... height (Ha) may not exceed good engineering practice as specified in 40 CFR 51.100(ii). (iii) If the TESH...) Noncarcinogenic metals. The feed rates of antimony, barium, lead, mercury, thallium, and silver in all feed..., barium, mercury, thallium, and silver are based on either: (A) An hourly rolling average as defined...

  4. 40 CFR 266.106 - Standards to control metals emissions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... height (Ha) may not exceed good engineering practice as specified in 40 CFR 51.100(ii). (iii) If the TESH...) Noncarcinogenic metals. The feed rates of antimony, barium, lead, mercury, thallium, and silver in all feed..., barium, mercury, thallium, and silver are based on either: (A) An hourly rolling average as defined...

  5. 40 CFR 266.106 - Standards to control metals emissions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... height (Ha) may not exceed good engineering practice as specified in 40 CFR 51.100(ii). (iii) If the TESH...) Noncarcinogenic metals. The feed rates of antimony, barium, lead, mercury, thallium, and silver in all feed..., barium, mercury, thallium, and silver are based on either: (A) An hourly rolling average as defined...

  6. Environment-dependent photochromism of silver nanoparticles interfaced with metal-oxide films

    NASA Astrophysics Data System (ADS)

    Fu, Shencheng; Sun, Shiyu; Zhang, Xintong; Zhang, Cen; Zhao, Xiaoning; Liu, Yichun

    2015-12-01

    Different metal-oxide films were fabricated by radio frequency magnetron sputtering. Further, a layer of silver nanoparticles (NPs) was deposited on the surface of the substrate by physical sputtering. Photochromism of the silver/metal-oxide nanocomposite films were investigated in situ under the irradiation of a linearly-polarized green laser beam (532 nm). Silver NPs were found to be easily photo-dissolved on the n-type metal-oxide films. By changing experimental conditions, it was also verified that both oxygen and humidity accelerate the photochromism of silver NPs. The corresponding micro-mechanism on charge separation and Ag+-ions mobility was also discussed. These results provided theoretical basis for the application of silver NPs in biological, chemical and medical areas.

  7. Stabilizing conditions of metal mercury in mercury sulfurization using a planetary ball mill.

    PubMed

    Fukuda, Naomichi; Takaoka, Masaki; Oshita, Kazuyuki; Mizuno, Tadao

    2014-07-15

    This study used a non-heating process to stabilize mercury by mercury sulfurization. Elemental mercury and sulfur were mixed using planetary ball milling under various experimental conditions and the optimal conditions were determined. The labile intermediate, mercury sulfide, was observed in the early stages of milling, and the intermediates were then pulverized into mercury sulfide powder. These phenomena were significantly influenced by the diameter of the planetary ball. A larger diameter enhanced mercury stabilization. For a ball with a 19.04-mm diameter, the toxicity characteristic leaching procedure (TCLP) and the Japanese leaching test (JLT) values were 0.263μg/L and 0.0586μg/L, respectively, suggesting that mercury leachability was strictly controlled. When the molar ratio of sulfur to mercury was 1.05, the mercury concentration in the headspace was <1μg/Nm(3) at 20°C, which was equivalent to the level in pure reagent. The stability of the planetary ball milling product at optimum conditions was either comparable or superior to that in other stabilization techniques. The running cost of this technology was estimated to be 15,360Yen (154USD)/ton-Hg. This stabilization technology is cost-effective and environmentally sound for the long-term and safe management of mercury. PMID:24929784

  8. Sulfidation kinetics of silver nanoparticles reacted with metal sulfides.

    PubMed

    Thalmann, Basilius; Voegelin, Andreas; Sinnet, Brian; Morgenroth, Eberhard; Kaegi, Ralf

    2014-05-01

    Recent studies have documented that the sulfidation of silver nanoparticles (Ag-NP), possibly released to the environment from consumer products, occurs in anoxic zones of urban wastewater systems and that sulfidized Ag-NP exhibit dramatically reduced toxic effects. However, whether Ag-NP sulfidation also occurs under oxic conditions in the absence of bisulfide has not been addressed, yet. In this study we, therefore, investigated whether metal sulfides that are more resistant toward oxidation than free sulfide, could enable the sulfidation of Ag-NP under oxic conditions. We reacted citrate-stabilized Ag-NP of different sizes (10-100 nm) with freshly precipitated and crystalline CuS and ZnS in oxygenated aqueous suspensions at pH 7.5. The extent of Ag-NP sulfidation was derived from the increase in dissolved Cu(2+) or Zn(2+) over time and linked with results from X-ray absorption spectroscopy (XAS) analysis of selected samples. The sulfidation of Ag-NP followed pseudo first-order kinetics, with rate coefficients increasing with decreasing Ag-NP diameter and increasing metal sulfide concentration and depending on the type (CuS and ZnS) and crystallinity of the reacting metal sulfide. Results from analytical electron microscopy revealed the formation of complex sulfidation patterns that seemed to follow preexisting subgrain boundaries in the pristine Ag-NP. The kinetics of Ag-NP sulfidation observed in this study in combination with reported ZnS and CuS concentrations and predicted Ag-NP concentrations in wastewater and urban surface waters indicate that even under oxic conditions and in the absence of free sulfide, Ag-NP can be transformed into Ag2S within a few hours to days by reaction with metal sulfides. PMID:24678586

  9. Brazing of copper to stainless steel with a low-silver-content brazing filler metal

    NASA Astrophysics Data System (ADS)

    Fukikoshi, Tatsuya; Watanabe, Yūki; Miyazawa, Yasuyuki; Kanasaki, Fumio

    2014-08-01

    The brazing of copper to stainless steel (SUS304 JIS) was performed using a low- silver-content brazing filler metal, Ag-50Cu, under an Ar gas atmosphere with a conventional furnace, owing to the potential economic benefits of using low-silver-content filler metals. The brazeability of the low-silver-content brazing filler metal to copper and SUS304 was investigated. A good joint was obtained, and a drastic dissolution reaction occurred at the copper side. Molten BAg8 penetrated along the crystal grain boundary of the copper base metal when BAg8 was used as the filler metal. This was caused by the dissolution of Ni from the stainless steel into the molten filler metal. Ag-50Cu, which was investigated in this work, can be used instead of BAg8 filler metal.

  10. Silver nanowires-templated metal oxide for broadband Schottky photodetector

    NASA Astrophysics Data System (ADS)

    Patel, Malkeshkumar; Kim, Hong-Sik; Park, Hyeong-Ho; Kim, Joondong

    2016-04-01

    Silver nanowires (AgNWs)-templated transparent metal oxide layer was applied for Si Schottky junction device, which remarked the record fastest photoresponse of 3.4 μs. Self-operating AgNWs-templated Schottky photodetector showed broad wavelength photodetection with high responsivity (42.4 A W-1) and detectivity (2.75 × 1015 Jones). AgNWs-templated indium-tin-oxide (ITO) showed band-to-band excitation due to the internal photoemission, resulting in significant carrier collection performances. Functional metal oxide layer was formed by AgNWs-templated from ITO structure. The grown ITO above AgNWs has a cylindrical shape and acts as a thermal protector of AgNWs for high temperature environment without any deformation. We developed thermal stable AgNWs-templated transparent oxide devices and demonstrated the working mechanism of AgNWs-templated Schottky devices. We may propose the high potential of hybrid transparent layer design for various photoelectric applications, including solar cells.

  11. Understanding Interactions between Cellular Matrices and Metal Complexes: Methods To Improve Silver Nanodot-Specific Staining.

    PubMed

    Choi, Sungmoon; Yu, Junhua

    2016-08-26

    Metal complexes are frequently used for biological applications due to their special photophysical and chemical characteristics. Due to strong interactions between metals and biomacromolecules, a random staining of cytoplasm or nucleoplasm by the complexes results in a low signal-to-background ratio. In this study, we used luminescent silver nanodots as a model to investigate the major driving force for non-specific staining in cellular matrices. Even though some silver nanodot emitters exhibited excellent specific staining of nucleoli, labeling with nanodots was problematic owing to severe non-specific staining. Binding between silver and sulfhydryl group of proteins appeared to be the major factor that enforced the silver staining. The oxidation of thiol groups in cells with hexacyanoferrate(III) dramatically weakened the silver-cell interaction and consequently significantly improved the efficiency of targeted staining. PMID:27380586

  12. Auto-aggressive metallic mercury injection around the knee joint: a case report

    PubMed Central

    2011-01-01

    Background Accidental or intentional subcutaneous and/or intramuscular injection of metallic mercury is an uncommon form of poisoning. Although it does not carry the same risk as mercury vapour inhalation, it may cause destructive early and late reactions. Case Presentation Herein we present the case of a 29-year-old male patient who developed an obsessive-compulsive disorder causing auto-aggressive behaviour with injection of elemental mercury and several other foreign bodies into the soft tissues around the left knee about 15 years before initial presentation. For clinical examination X-rays and a CT-scan of the affected area were performed. Furthermore, blood was taken to determine the mercury concentration in the blood, which showed a concentration 17-fold higher than recommended. As a consequence, the mercury depots and several foreign bodies were resected marginally. Conclusion Blood levels of mercury will decrease rapidly following surgery, especially in combination with chelating therapy. In case of subcutaneous and intramuscular injection of metallic mercury we recommend marginal or wide excision of all contaminated tissue to prevent migration of mercury and chronic inflammation. Nevertheless, prolonged clinical and biochemical monitoring should be performed for several years to screen for chronic intoxication. PMID:22093686

  13. Use of Mercury in Dental Silver Amalgam: An Occupational and Environmental Assessment

    PubMed Central

    Jamil, Nadia; Ilyas, Samar; Qadir, Abdul; Arslan, Muhammad; Salman, Muhammad; Ahsan, Naveed; Zahid, Hina

    2016-01-01

    The objective of this study was to assess the occupational exposure to mercury in dentistry and associated environmental emission in wastewater of Lahore, Pakistan. A total of ninety-eight blood samples were collected comprising 37 dentists, 31 dental assistants, and 30 controls. Results demonstrate that the dentistry personnel contained significantly higher mean concentration of mercury in their blood samples (dentists: 29.835 µg/L and dental assistants: 22.798 µg/L) compared to that of the controls (3.2769 µg/L). The mean concentration of mercury was found maximum in the blood samples of older age group (62.8 µg/L) in dentists and (44.3 µg/L) in dental assistants. The comparison of mercury concentration among dentists, dental assistants, and controls (pairing based on their ages) revealed that the concentration increased with the age and experience among the dentists and dental assistants. Moreover, the mercury concentration in all the studied dental wastewater samples, collected from twenty-two dental clinics, was found to be exceeding the recommended discharge limit of 0.01 mg/L. Therefore, we recommend that immediate steps must be taken to ensure appropriate preventive measures to avoid mercury vapors in order to prevent potential health hazards to dentistry personnel. Strong regulatory and administrative measures are needed to deal with mercury pollution on emergency basis. PMID:27446955

  14. Use of Mercury in Dental Silver Amalgam: An Occupational and Environmental Assessment.

    PubMed

    Jamil, Nadia; Baqar, Mujtaba; Ilyas, Samar; Qadir, Abdul; Arslan, Muhammad; Salman, Muhammad; Ahsan, Naveed; Zahid, Hina

    2016-01-01

    The objective of this study was to assess the occupational exposure to mercury in dentistry and associated environmental emission in wastewater of Lahore, Pakistan. A total of ninety-eight blood samples were collected comprising 37 dentists, 31 dental assistants, and 30 controls. Results demonstrate that the dentistry personnel contained significantly higher mean concentration of mercury in their blood samples (dentists: 29.835 µg/L and dental assistants: 22.798 µg/L) compared to that of the controls (3.2769 µg/L). The mean concentration of mercury was found maximum in the blood samples of older age group (62.8 µg/L) in dentists and (44.3 µg/L) in dental assistants. The comparison of mercury concentration among dentists, dental assistants, and controls (pairing based on their ages) revealed that the concentration increased with the age and experience among the dentists and dental assistants. Moreover, the mercury concentration in all the studied dental wastewater samples, collected from twenty-two dental clinics, was found to be exceeding the recommended discharge limit of 0.01 mg/L. Therefore, we recommend that immediate steps must be taken to ensure appropriate preventive measures to avoid mercury vapors in order to prevent potential health hazards to dentistry personnel. Strong regulatory and administrative measures are needed to deal with mercury pollution on emergency basis. PMID:27446955

  15. [Mercury (and...) through the centuries].

    PubMed

    Kłys, Małgorzata

    2010-01-01

    Mercury has a long history, fascinating in its many aspects. Through the centuries--from ancient times to the present day--the metal in its various forms, also known under the name "quicksilver", accompanied the man and was used for diversified purposes. Today, mercury is employed in manufacturing thermometers, barometers, vacuum pumps and explosives. It is also used in silver and gold mining processes. Mercury compounds play a significant role in dentistry, pharmaceutical industry and crop protection. The contemporary use of mercury markedly decreases, but historically speaking, the archives abound in materials that document facts and events occurring over generations and the immense intellectual effort aiming at discovering the true properties and mechanisms of mercury activity. Mercury toxicity, manifested in destruction of biological membranes and binding of the element with proteins, what disturbs biochemical processes occurring in the body, was discovered only after many centuries of the metal exerting its effect on the lives of individuals and communities. For centuries, mercury was present in the work of alchemists, who searched for the universal essence or quintessence and the so-called philosopher's stone. In the early modern era, between the 16th and 19th centuries, mercury was used to manufacture mirrors. Mercury compounds were employed as a medication against syphilis, which plagued mankind for more than four hundred years--from the Middle Ages till mid 20th century, when the discovery of penicillin became the turning point. This extremely toxic therapy resulted in much suffering, individual tragedies, chronic poisonings leading to fatalities and dramatic sudden deaths. In the last fifty years, there even occurred attempts of mentally imbalanced individuals at injecting themselves with metallic mercury, also as a performance-enhancing drug. Instances of mass mercury poisoning occurred many times in the past in consequence of eating food products

  16. Mercury

    MedlinePlus

    ... be found in: Batteries Chemistry labs Some disinfectants Folk remedies Red cinnabar mineral Organic mercury can be ... heart tracing Fluids through a vein (by IV) Medicine to treat symptoms The type of exposure will ...

  17. Development of silver/gold nanocages onto indium tin oxide glass as a reagentless plasmonic mercury sensor.

    PubMed

    Huang, Daodan; Hu, Tingting; Chen, Na; Zhang, Wei; Di, Junwei

    2014-05-12

    We demonstrate the utilization of silver/gold nanocages (Ag/Au NCs) deposited onto transparent indium tin oxide (ITO) film glass as the basis of a reagentless, simple and inexpensive mercury probe. The localized surface plasmon resonance (LSPR) peak wavelength was located at ∼800 nm. By utilizing the redox reaction between Hg(2+) ions and Ag atoms that existed in Ag/Au NCs, the LSPR peak of Ag/Au NCs was blue-shifted. Thus, we develop an optical sensing probe for the detection of Hg(2+) ions. The LSPR peak changes were lineally proportional to the concentration of Hg(2+) ions over the range from 10 ppb to 0.5 ppm. The detection limit was ∼5 ppb. This plasmonic probe shows good selectivity and high sensitivity. The proposed optical probe is successfully applied to the sensing of Hg(2+) in real samples. PMID:24767150

  18. Cases of mercury exposure, bioavailability, and absorption.

    PubMed

    Gochfeld, Michael

    2003-09-01

    Mercury is a unique element that, unlike many metals, has no essential biological function. It is liquid at room temperature and is 13.6 times heavier than water. Its unique physical properties have been exploited for a variety of uses such as in mercury switches, thermostats, thermometers, and other instruments. Its ability to amalgamate with gold and silver are used in mining these precious metals and as a dental restorative. Its toxic properties have been exploited for medications, preservatives, antiseptics, and pesticides. For these reasons there have been many industrial uses of mercury, and occupational exposures of workers and industrial emissions and effluents contaminating air, water, soil, and ultimately food chains have long been a matter of great public health concern. This paper examines briefly six cases representing various forms of exposure to different species of mercury, and indicates the methodological issues in estimating exposure, bioavailability and absorption; these cases include Minamata disease in Japan, organic mercury poisoning in Iraq, methylmercury (MeHg) exposure in the Amazon, dimethylmercury (PMM) in the laboratory, an elemental mercury spill in Cajamarca, Peru, and a mercury-contaminated building in Hoboken, NJ, USA. Other scenarios that are not described include occupational exposure to mercury salts, mercurial preservatives in vaccines, cultural and ritualistic uses of mercury, and mercury in dental amalgams. PMID:12915150

  19. Optimization of method for zinc analysis in several bee products on renewable mercury film silver based electrode.

    PubMed

    Opoka, Włodzimierz; Szlósarczyk, Marek; Maślanka, Anna; Piech, Robert; Baś, Bogusław; Włodarczyk, Edyta; Krzek, Jan

    2013-01-01

    Zinc is an interesting target for detection as it is one of the elements necessary for the proper functioning of the human body, its excess and deficiency can cause several symptoms. Several techniques including electrochemistry have been developed but require laboratory equipment, preparative steps and mercury or complex working electrodes. We here described the development of a robust, simple and commercially available electrochemical system. Differential pulse (DP) voltammetry was used for this purpose with the cyclic renewable mercury film silver based electrode (Hg(Ag)FE) and 0.05 M KNO3 solution as a supporting electrolyte. The effect of various factors such as: preconcentration potential and time, pulse amplitude and width, step potential and supporting electrolyte composition are optimized. The limits of detection (LOD) and quantification (LOQ) were 1.62 ng/mL and 4.85 ng/mL, respectively. The repeatability of the method at a concentration level of the analyte as low as 3 ng/mL, expressed as RSD is 3.5% (n = 6). Recovery was determined using certified reference material: Virginia Tobacco Leaves (CTA-VTL-2). The recovery of zinc ranged from 96.6 to 106.5%. The proposed method was successfully applied for determination of zinc in bee products (honey, propolis and diet supplements) after digestion procedure. PMID:24383319

  20. Noble Metal Catalysts for Mercury Oxidation in Utility Flue Gas: Gold, Palladium and Platinum Formulations

    SciTech Connect

    Presto, A.A.; Granite, E.J

    2008-07-01

    The use of noble metals as catalysts for mercury oxidation in flue gas remains an area of active study. To date, field studies have focused on gold and palladium catalysts installed at pilot scale. In this article, we introduce bench-scale experimental results for gold, palladium and platinum catalysts tested in realistic simulated flue gas. Our initial results reveal some intriguing characteristics of catalytic mercury oxidation and provide insight for future research into this potentially important process.

  1. IMPACT OF NOBLE METALS AND MERCURY ON HYDROGEN GENERATION DURING HIGH LEVEL WASTE PRETREATMENT AT THE SAVANNAH RIVER SITE

    SciTech Connect

    Stone, M; Tommy Edwards, T; David Koopman, D

    2009-03-03

    The Defense Waste Processing Facility (DWPF) at the Savannah River Site vitrifies radioactive High Level Waste (HLW) for repository internment. The process consists of three major steps: waste pretreatment, vitrification, and canister decontamination/sealing. HLW consists of insoluble metal hydroxides (primarily iron, aluminum, calcium, magnesium, manganese, and uranium) and soluble sodium salts (carbonate, hydroxide, nitrite, nitrate, and sulfate). The pretreatment process in the Chemical Processing Cell (CPC) consists of two process tanks, the Sludge Receipt and Adjustment Tank (SRAT) and the Slurry Mix Evaporator (SME) as well as a melter feed tank. During SRAT processing, nitric and formic acids are added to the sludge to lower pH, destroy nitrite and carbonate ions, and reduce mercury and manganese. During the SME cycle, glass formers are added, and the batch is concentrated to the final solids target prior to vitrification. During these processes, hydrogen can be produced by catalytic decomposition of excess formic acid. The waste contains silver, palladium, rhodium, ruthenium, and mercury, but silver and palladium have been shown to be insignificant factors in catalytic hydrogen generation during the DWPF process. A full factorial experimental design was developed to ensure that the existence of statistically significant two-way interactions could be determined without confounding of the main effects with the two-way interaction effects. Rh ranged from 0.0026-0.013% and Ru ranged from 0.010-0.050% in the dried sludge solids, while initial Hg ranged from 0.5-2.5 wt%, as shown in Table 1. The nominal matrix design consisted of twelve SRAT cycles. Testing included: a three factor (Rh, Ru, and Hg) study at two levels per factor (eight runs), three duplicate midpoint runs, and one additional replicate run to assess reproducibility away from the midpoint. Midpoint testing was used to identify potential quadratic effects from the three factors. A single sludge

  2. Principal Locations of Metal Loading from Flood-Plain Tailings, Lower Silver Creek, Utah, April 2004

    USGS Publications Warehouse

    Kimball, Briant A.; Runkel, Robert L.; Walton-Day, Katherine

    2007-01-01

    Because of the historical deposition of mill tailings in flood plains, the process of determining total maximum daily loads for streams in an area like the Park City mining district of Utah is complicated. Understanding the locations of metal loading to Silver Creek and the relative importance of these locations is necessary to make science-based decisions. Application of tracer-injection and synoptic-sampling techniques provided a means to quantify and rank the many possible source areas. A mass-loading study was conducted along a 10,000-meter reach of Silver Creek, Utah, in April 2004. Mass-loading profiles based on spatially detailed discharge and chemical data indicated five principal locations of metal loading. These five locations contributed more than 60 percent of the cadmium and zinc loads to Silver Creek along the study reach and can be considered locations where remediation efforts could have the greatest effect upon improvement of water quality in Silver Creek.

  3. Copper-silver-titanium filler metal for direct brazing of structural ceramics

    DOEpatents

    Moorhead, Arthur J.

    1987-01-01

    A method of joining ceramics and metals to themselves and to one another is described using a brazing filler metal consisting essentially of 35 to 50 atomic percent copper, 15 to 50 atomic percent silver and 10 to 45 atomic percent titanium. This method produces strong joints that can withstand high service temperatures and oxidizing environments.

  4. Copper-silver-titanium-tin filler metal for direct brazing of structural ceramics

    DOEpatents

    Moorhead, Arthur J.

    1988-04-05

    A method of joining ceramics and metals to themselves and to one another at about 800.degree. C. is described using a brazing filler metal consisting essentially of 35 to 50 at. % copper, 40 to 50 at. % silver, 1 to 15 at. % titanium, and 2 to 8 at. % tin. This method produces strong joints that can withstand high service temperatures and oxidizing environments.

  5. Electroless silver plating for metallization of near-field optical fiber probes

    NASA Astrophysics Data System (ADS)

    Li, Chang'an; Xu, Lina; Gu, Ning

    2007-10-01

    By using mercaptopropyltrimethoxysilane (MPTS) self-assembled monolayers (SAMs), electroless silver plating is developed for the metallization of near-field optical fiber probes. This method has the advantages of controllability, no pinholes, convenience, low cost, and smooth tip surface. The metallized probes are characterized by optical microscopy, scanning electron microscopy (SEM), and energy dispersive X-ray spectroscopy (EDXS).

  6. Electrospun metal oxide-TiO2 nanofibers for elemental mercury removal from flue gas.

    PubMed

    Yuan, Yuan; Zhao, Yongchun; Li, Hailong; Li, Yang; Gao, Xiang; Zheng, Chuguang; Zhang, Junying

    2012-08-15

    Nanofibers prepared by an electrospinning method were used to remove elemental mercury (Hg(0)) from simulated coal combustion flue gas. The nanofibers composed of different metal oxides (MO(x)) including CuO, In(2)O(3), V(2)O(5), WO(3) and Ag(2)O supported on TiO(2) have been characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), energy dispersing X-ray (EDX) and UV-vis spectra. The average diameters of these nanofibers were about 200nm. Compared to pure TiO(2), the UV-vis absorption intensity for MO(x)-TiO(2) increased significantly and the absorption bandwidth also expanded, especially for Ag(2)O-TiO(2) and V(2)O(5)-TiO(2). Hg(0) oxidation efficiencies over the MO(x)-TiO(2) nanofibers were tested under dark, visible light (vis) irradiation and UV irradiation, respectively. The results showed that WO(3) doped TiO(2) exhibited the highest Hg(0) removal efficiency of 100% under UV irradiation. Doping V(2)O(5) into TiO(2) enhanced Hg(0) removal efficiency greatly from 6% to 63% under visible light irradiation. Ag(2)O doped TiO(2) showed a steady Hg(0) removal efficiency of around 95% without any light due to the formation of silver amalgam. An extended experiment with 8 Hg(0) removal cycles showed that the MO(x)-TiO(2) nanofibers were stable for removing Hg(0) from flue gas. Factors responsible for the enhanced photocatalytic activities of the MO(x)-TiO(2) nanofibers were also discussed. PMID:22703732

  7. Electrical and materials characterization of tungsten-titanium diffusion barrier layers and alloyed silver metallization

    NASA Astrophysics Data System (ADS)

    Bhagat, Shekhar Kumar

    With the constant miniaturization of semiconductor devices, research is always ongoing to obtain the best materials and/or materials systems which fulfill all the requirements of an ideal interconnect. Silver (Ag) and silver based alloys are front runners among other metals and alloys being investigated. Ag has a low electrical resistivity (1.59 micro-ohm-centimeters for bulk), very high thermal conductivity (4.25 Watt per centimeters per Kelvin), and has better electromigration resistance than aluminum (Al). In the pure form, however, it has several drawbacks (e.g., a tendency to diffuse in silicon substrate at higher temperatures, inadequate adhesion to silicon dioxide, poor corrosion resistance, and agglomeration at higher temperatures). These drawbacks can be circumvented by the addition of diffusion barrier layers and/or alloying in silver. The present study investigates both routes to make silver a legitimate interconnect material. Initially this study focuses on thermal stability and behavior of tungsten-titanium (W-Ti) barrier layers for Ag metallization. It is shown that Ag thin films are thermally stable up to 650 degrees centigrade with the presence of W-Ti under layers. The effect of a W-Ti layer on the {111} texture formation in Ag thin film is also evaluated in detail. Insertion of a thin W-Ti over layer on Ag thin films is investigated with respect to their thermal stability. This research also evaluates the diffusion of Ag into silicon dioxide and W-Ti barriers. This project shows that W-Ti is an effective barrier layer for silver metallization. Later, the study investigates the effect of Cu addition in silver metallization and its impact on electromigration resistance. It is shown that Cu addition enhances the electromigration lifetime for silver metallization.

  8. Alginate stabilized silver nanocube-Rh6G composite as a highly selective mercury sensor in aqueous solution

    NASA Astrophysics Data System (ADS)

    Tharmaraj, Vairaperumal; Pitchumani, Kasi

    2011-03-01

    Alginate-stabilized silver nanocubes are synthesized via a reduction method and are characterized by UV-Vis and fluorescence spectroscopies, SEM, AFM and HRTEM analyses. A silver nanocubes (Ag NCbs) based sensor for detecting Hg2+ ions in aqueous solution has been developed using Rh6G as an external spectroscopic probe. Using this system, Hg2+ ions (as low as 1 × 10-10 mol L-1) are recognized in aqueous media via a colorimetric method with very high selectivity and sensitivity over other metal ions namely Fe2+, Zn2+, Pb2+, Cu2+, Sn2+, Cd2+, Ni2+, and Co2+.Alginate-stabilized silver nanocubes are synthesized via a reduction method and are characterized by UV-Vis and fluorescence spectroscopies, SEM, AFM and HRTEM analyses. A silver nanocubes (Ag NCbs) based sensor for detecting Hg2+ ions in aqueous solution has been developed using Rh6G as an external spectroscopic probe. Using this system, Hg2+ ions (as low as 1 × 10-10 mol L-1) are recognized in aqueous media via a colorimetric method with very high selectivity and sensitivity over other metal ions namely Fe2+, Zn2+, Pb2+, Cu2+, Sn2+, Cd2+, Ni2+, and Co2+. Electronic supplementary information (ESI) available: Additional information concerning UV-Vis and emission spectra of alginate-Ag NCbs, 2D and 3D AFM images of alginate-Ag NCbs, 3D AFM image of alginate-Ag NCbs-Rh6G with the absence and presence of Hg2+. See DOI: 10.1039/c0nr00749h

  9. Silver-modified clinoptilolite for the removal of Escherichia coli and heavy metals from aqueous solutions.

    PubMed

    Akhigbe, Lulu; Ouki, Sabeha; Saroj, Devendra; Lim, Xiang Min

    2014-09-01

    This paper investigates the potential of using the silver antibacterial properties combined with the metal ion exchange characteristics of silver-modified clinoptilolite to produce a treatment system capable of removing both contaminants from aqueous streams. The results have shown that silver-modified clinoptilolite is capable of completely eliminating Escherichia coli after 30-min contact time demonstrating its effectiveness as a disinfectant. Systems containing both E. coli and metals exhibited 100 % E. coli reduction after 15-min contact time and maximum metal adsorption removal efficiencies of 97, 98, and 99 % for Pb(2+), Cd(2+), and Zn(2+) respectively after 60 min; 0.182-0.266 mg/g of metal ions were adsorbed by the zeolites in the single- and mixed-metal-containing solutions. Nonmodified clinoptilolite showed no antibacterial properties. This study demonstrated that silver-modified clinoptilolite exhibited high disinfection and heavy metal removal efficiencies and consequently could provide an effective combined treatment system for the removal of E. coli and metals from contaminated water streams. PMID:24756684

  10. Silver

    Integrated Risk Information System (IRIS)

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

  11. Reflective and Electrically Conductive Surface Silvered Polyimide Films and Coatings Prepared via Unusual Single-Stage Self-Metallization Techniques

    NASA Technical Reports Server (NTRS)

    Southward, Robin E.; Stoakley, Diane M.

    2001-01-01

    Highly reflective and/or surface conductive flexible polyimide films can be prepared by the incorporation of positive valent silver compounds into solutions of poly(amic acid)s formed from a variety of dianhydrides and diamines. Thermal curing of selected silver(I)-containing poly(amic acid)s leads to cycloimidization of the polyimide precursor with concomitant silver(I) reduction and surface aggregation of the metal yielding a reflective and/or conductive silver surface similar to that of the native metal. However, not all silver(I) precursors are effective surface metallization agents and not all poly(amic acid)s metallize with equal facility. Ligand/anion and polyimide structural effects on film metallization efficacy and on physical properties on metallized films are reviewed.

  12. Method for fixating sludges and soils contaminated with mercury and other heavy metals

    DOEpatents

    Broderick, Thomas E.; Roth, Rachel L.; Carlson, Allan L.

    2005-06-28

    The invention relates to a method, composition and apparatus for stabilizing mercury and other heavy metals present in a particulate material such that the metals will not leach from the particulate material. The method generally involves the application of a metal reagent, a sulfur-containing compound, and the addition of oxygen to the particulate material, either through agitation, sparging or the addition of an oxygen-containing compound.

  13. Bacterial Killing by Light-Triggered Release of Silver from Biomimetic Metal Nanorods

    PubMed Central

    Yi, Ji; Zhang, Ran; Rivera, José G.; Messersmith, Phillip B.

    2014-01-01

    Illumination of noble metal nanoparticles at the plasmon resonance causes substantial heat generation, and the transient and highly localized temperature increases that result from this energy conversion can be exploited for photothermal therapy by plasmonically heating gold nanorods (NRs) bound to cell surfaces. Here, we report the first use of plasmonic heating to locally release silver from gold core/silver shell (Au@Ag) NRs targeted to bacterial cell walls. A novel biomimetic method of preparing Au@Ag core-shell NRs was employed, involving deposition of a thin organic polydopamine (PD) primer onto Au NR surfaces, followed by spontaneous electroless silver metallization, and conjugation of antibacterial antibodies and passivating polymers for targeting to gram-negative and gram-positive bacteria. Dramatic cytotoxicity of S. epidermidis and E. coli cells targeted with Au@Ag NRs was observed upon exposure to light as a result of the combined antibacterial effects of plasmonic heating and silver release. The antibacterial effect was much greater than with either plasmonic heating or silver alone, implying a strong therapeutic synergy between cell-targeted plasmonic heating and the associated silver release upon irradiation. Our findings suggest a potential antibacterial use of Au@Ag NRs when coupled with light irradiation, which was not previously described. PMID:23847147

  14. Analysis of metals with luster: Roman brass and silver

    NASA Astrophysics Data System (ADS)

    Fajfar, H.; Rupnik, Z.; Šmit, Ž.

    2015-11-01

    Non-destructive PIXE analysis using in-air proton beam was used for the studies of earliest brass coins issued during the 1st century BC by Greek cities in Asia Minor, Romans and Celts, and for the studies of plated low grade silver coins of the 3rd century AD. The analysis determined the levels of zinc and important trace elements, notably selenium, which confirms spread of selenium-marked copper from the east. For plating, combined tinning and silvering was identified by the mapping technique for the mid 3rd century AD, which evolved into mere plating by 270 AD.

  15. Mercury

    NASA Technical Reports Server (NTRS)

    Gault, D. E.; Burns, J. A.; Cassen, P.; Strom, R. G.

    1977-01-01

    Prior to the flight of the Mariner 10 spacecraft, Mercury was the least investigated and most poorly known terrestrial planet (Kuiper 1970, Devine 1972). Observational difficulties caused by its proximity to the Sun as viewed from Earth caused the planet to remain a small, vague disk exhibiting little surface contrast or details, an object for which only three major facts were known: 1. its bulk density is similar to that of Venus and Earth, much greater than that of Mars and the Moon; 2. its surface reflects electromagnetic radiation at all wavelengths in the same manner as the Moon (taking into account differences in their solar distances); and 3. its rotation period is in 2/3 resonance with its orbital period. Images obtained during the flyby by Mariner 10 on 29 March 1974 (and the two subsequent flybys on 21 September 1974 and 16 March 1975) revealed Mercury's surface in detail equivalent to that available for the Moon during the early 1960's from Earth-based telescopic views. Additionally, however, information was obtained on the planet's mass and size, atmospheric composition and density, charged-particle environment, and infrared thermal radiation from the surface, and most significantly of all, the existence of a planetary magnetic field that is probably intrinsic to Mercury was established. In the following, this new information is summarized together with results from theoretical studies and ground-based observations. In the quantum jumps of knowledge that have been characteristic of "space-age" exploration, the previously obscure body of Mercury has suddenly come into sharp focus. It is very likely a differentiated body, probably contains a large Earth-like iron-rich core, and displays a surface remarkably similar to that of the Moon, which suggests a similar evolutionary history.

  16. Label free and high specific detection of mercury ions based on silver nano-liposome

    NASA Astrophysics Data System (ADS)

    Priyadarshini, Eepsita; Pradhan, Nilotpala; Pradhan, Arun K.; Pradhan, Pallavi

    2016-06-01

    Herein, we report an eco-friendly, mild and one-pot approach for synthesis of silver nanoparticles via a lipopeptide biosurfactant - CHBS. The biosurfactant forms liposome vesicles when dispersed in an aqueous medium. The amino acid groups of the biosurfactant assists in the reduction of Ag+ ions leading to the production of homogeneous silver nanoparticles, encapsulated within the liposome vesicle, as confirmed from TEM analysis. Rate of synthesis and size of particle were greatly dependent on pH and reaction temperature. Kinetic analysis suggests the involvement of an autocatalytic reaction and the observed rate constant (kobs) was found to decrease with temperature, suggesting faster reaction with increasing temperature. Furthermore, the silver nanoparticles served as excellent probes for highly selective and sensitive recognition of Hg2 + ions. Interaction with Hg2 + ions results in an immediate change in colour of nanoparticle solution form brownish red to milky white. With increasing Hg2 + ions concentration, a gradual disappearance of SPR peak was observed. A linear relationship (A420/660) with an R2 value of 0.97 was observed in the range of 20 to 100 ppm Hg2 + concentration. Hg2 + ions are reduced to their elemental forms which thereby interact with the vesicles, leading to aggregation and precipitation of particles. The detection method avoids the need of functionalizing ligands and favours Hg2 + detection in aqueous samples by visible range spectrophotometry and hence can be used for simple and rapid analysis.

  17. Label free and high specific detection of mercury ions based on silver nano-liposome.

    PubMed

    Priyadarshini, Eepsita; Pradhan, Nilotpala; Pradhan, Arun K; Pradhan, Pallavi

    2016-06-15

    Herein, we report an eco-friendly, mild and one-pot approach for synthesis of silver nanoparticles via a lipopeptide biosurfactant - CHBS. The biosurfactant forms liposome vesicles when dispersed in an aqueous medium. The amino acid groups of the biosurfactant assists in the reduction of Ag(+) ions leading to the production of homogeneous silver nanoparticles, encapsulated within the liposome vesicle, as confirmed from TEM analysis. Rate of synthesis and size of particle were greatly dependent on pH and reaction temperature. Kinetic analysis suggests the involvement of an autocatalytic reaction and the observed rate constant (kobs) was found to decrease with temperature, suggesting faster reaction with increasing temperature. Furthermore, the silver nanoparticles served as excellent probes for highly selective and sensitive recognition of Hg(2+) ions. Interaction with Hg(2+) ions results in an immediate change in colour of nanoparticle solution form brownish red to milky white. With increasing Hg(2+) ions concentration, a gradual disappearance of SPR peak was observed. A linear relationship (A420/660) with an R(2) value of 0.97 was observed in the range of 20 to 100ppm Hg(2+) concentration. Hg(2+) ions are reduced to their elemental forms which thereby interact with the vesicles, leading to aggregation and precipitation of particles. The detection method avoids the need of functionalizing ligands and favours Hg(2+) detection in aqueous samples by visible range spectrophotometry and hence can be used for simple and rapid analysis. PMID:27045785

  18. Preparation of Highly Dispersed Conductive Metals for Electronic Applications: Silver and Copper

    NASA Astrophysics Data System (ADS)

    LaPlante, Sylas C.

    This study focuses on the development of different methods to prepare conductive particles for electronic applications. Although it has been shown that metallic particles can be prepared by physical and thermal processes, the most versatile approach remains the chemical precipitation in homogeneous solutions. This preparation route provides an excellent control over key experimental parameters such as type of solvent, reducing species, complexing species and dispersing agents and allows unparalleled ability for tailoring the final particle properties. The metals chosen for this study are silver and copper, as they are the most widely used materials to 'construct' conductive structures in the electronics industry. This dissertation introduces three environmentally friendly methods to prepare conductive particles which are industrially scalable and most notably used in electronic applications. In the first part, we describe a novel method to prepare dispersed crystalline copper particles by reacting aqueous dispersions of CuCl with ferrous citrate. We report that the Fe (II) citrate complex can reduce rapidly and completely cuprous chloride to metallic copper and propose a mechanism for the reaction observed. By changing the precipitation conditions, copper particles with sizes varying from 250 nm to 2.0 microns were obtained. The method described represents a simple and versatile approach for preparing copper powders for electronic applications. In the second part, a novel environmentally friendly solution-based method for preparing dispersed silver particles is described. The simple and convenient approach consists in heating silver oxide particles dispersed in a highly alkaline water/acetone mixture. The data presented clearly show that acetone reduces completely and rapidly Ag2O particles to metallic silver at 60 °C. A mechanism explaining the provenance of the electrons responsible for the reduction of silver is proposed. Finally, in the third part, a strategy

  19. 40 CFR 63.10885 - What are my management practices for metallic scrap and mercury switches?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... implementing subtitle C of the Resource Conservation and Recovery Act (RCRA) (40 CFR parts 261 through 265 and... rules implementing subtitle C of RCRA (40 CFR parts 261 through 265 and 268). The progress reports must... metallic scrap and mercury switches? 63.10885 Section 63.10885 Protection of Environment...

  20. 40 CFR 63.10885 - What are my management practices for metallic scrap and mercury switches?

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... implementing subtitle C of the Resource Conservation and Recovery Act (RCRA) (40 CFR parts 261 through 265 and... rules implementing subtitle C of RCRA (40 CFR parts 261 through 265 and 268). The progress reports must... metallic scrap and mercury switches? 63.10885 Section 63.10885 Protection of Environment...

  1. 40 CFR 63.10885 - What are my management practices for metallic scrap and mercury switches?

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... implementing subtitle C of the Resource Conservation and Recovery Act (RCRA) (40 CFR parts 261 through 265 and... rules implementing subtitle C of RCRA (40 CFR parts 261 through 265 and 268). The progress reports must... metallic scrap and mercury switches? 63.10885 Section 63.10885 Protection of Environment...

  2. 40 CFR 63.10885 - What are my management practices for metallic scrap and mercury switches?

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... implementing subtitle C of the Resource Conservation and Recovery Act (RCRA) (40 CFR parts 261 through 265 and... rules implementing subtitle C of RCRA (40 CFR parts 261 through 265 and 268). The progress reports must... metallic scrap and mercury switches? 63.10885 Section 63.10885 Protection of Environment...

  3. 40 CFR 63.10885 - What are my management practices for metallic scrap and mercury switches?

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... implementing subtitle C of the Resource Conservation and Recovery Act (RCRA) (40 CFR parts 261 through 265 and... rules implementing subtitle C of RCRA (40 CFR parts 261 through 265 and 268). The progress reports must... metallic scrap and mercury switches? 63.10885 Section 63.10885 Protection of Environment...

  4. Preparation of novel mercury-doped silver nanoparticles film glassy carbon electrode and its application for electrochemical biosensor.

    PubMed

    Li, Mao-Guo; Shang, Yong-Jia; Gao, Ying-Chun; Wang, Guang-Feng; Fang, Bin

    2005-06-01

    A novel mercury-doped silver nanoparticles film glassy carbon (Ag/MFGC) electrode was prepared in this study. Electrochemical behaviors of cysteine on the Ag/MFGC electrode were investigated by electrochemical impedance spectroscopy and cyclic voltammetry (CV). The results indicated that cysteine could be strongly adsorbed on the surface of the Ag/MFGC electrode to form a thin layer. The doped electrode could catalyze the electrode reaction process of cysteine, and the cysteine displayed a pair of well-defined and nearly reversible CV peaks at the electrode in an acetate buffer solution (pH 5.0). The Ag/MFGC electrode was used for determination of cysteine by differential pulse voltammetry. The linear range was between 4.0x10(-7) and 1.3x10(-5) mol/L, with a detection limit of 1.0x10(-7) mol/L and a signal-to-noise ratio of 3. The relative standard deviation was 2.4% for seven successive determinations of 1.0x10(-5) mol/L cysteine. The determinations of cysteine in synthetic samples and urinal samples were carried out and satisfactory results were obtained. Amperometric application of the Ag/MFGC electrode as biosensors is proposed. PMID:15866527

  5. Notes from the Field: Acute Mercury Poisoning After Home Gold and Silver Smelting--Iowa, 2014.

    PubMed

    Koirala, Samir; Leinenkugel, Kathy

    2015-12-18

    In March 2014, a man, aged 59 years, who lived alone and had been using different smelting techniques viewed on the Internet to recover gold and silver from computer components, was evaluated at a local emergency department for shortness of breath, tremors, anorexia, and generalized weakness. During the smelting processes, he had used hydrogen peroxide, nitric acid, muriatic acid, and sulfuric acid purchased from local stores or Internet retailers. For protection, he wore a military gas mask of unknown type. The mask was used with filter cartridges, but their effectiveness against chemical fumes was not known. PMID:26678598

  6. Carbon Solubility in Silicon-Iron-Bearing Metals during Core Formation on Mercury

    NASA Technical Reports Server (NTRS)

    Vander Kaaden, Kathleen E.; McCubbin, Francis M.; Ross, D. Kent; Rapp, Jennifer F.; Danielson, Lisa R.; Keller, Lindsay P.; Righter, Kevin

    2016-01-01

    Recent results obtained from the MErcury Surface, Space ENvironment, GEochemistry, and Ranging (MESSENGER) spacecraft showed the surface of Mercury has high S abundances (approximately 4 wt%) and low Iron(II) Oxide abundances (less than 2 wt%). Based on these extreme values, the oxygen fugacity of Mercury's surface materials was estimated to be approximately 3 to 7 log(sub 10) units below the IW buffer (Delta IW-3 to Delta IW-7). This highly reducing nature of the planet has resulted in a large core and relatively thin mantle, extending to only approximately 420 km depth (corresponding to a core-mantle boundary pressure of approximately 4-7 GPa) within the planet. Furthermore, MESSENGER results have suggested the presence of carbon on the surface of the planet. Previous experimental results from have also suggested the possibility of a primary floatation crust on Mercury composed of graphite, produced after a global magma ocean event. With these exotic conditions of this compositional end-member planet, it begs the question, what is the core composition of Mercury? Although no definitive conclusion has been reached, previous studies have made advances towards answering this question. Riner et al. and Chen et al. looked at iron sulfide systems and implemented various crystallization and layered core scenarios to try and determine the composition and structure of Mercury's core. Malavergne et al. examined core crystallization scenarios in the presence of sulfur and silicon. Hauck et al. used the most recent geophysical constraints from the MESSENGER spacecraft to model the internal structure of Mercury, including the core, in a iron-sulfur-silicon system. More recently, Chabot et al. conducted a series of metal-silicate partitioning experiments in a iron-sulfur-silicon system. These results showed the core of Mercury has the potential to contain more than 15 wt% silicon. However, with the newest results from MESSENGER's low altitude campaign, carbon is another

  7. ARSENIC DETERMINATION BY THE SILVER DIETHYLDITHIOCARBAMATE METHOD AND THE ELIMINATION OF METAL ION INTERFERENCE

    EPA Science Inventory

    The interference of metals with the determination of arsenic by the silver diethyldithiocarbamate (SDDC) Method was investigated. Low recoveries of arsenic are obtained when cobalt, chromium, molybdenum, nitrate, nickel or phosphate are at concentrations of 7 mg/l or above (indiv...

  8. Mod silver metallization: Screen printing and ink-jet printing

    NASA Technical Reports Server (NTRS)

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

    1985-01-01

    Basic material efforts have proven to be very successful. Adherent and conductive films were achieved. A silver neodecanoate/bismuth 2-ethylhexanoate mixture has given the best results in both single and double layer applications. Another effort is continuing to examine the feasibility of applying metallo-organic deposition films by use of an ink jet printer. Direct line writing would result in a saving of process time and materials. So far, some well defined lines have been printed.

  9. Mod silver metallization: Screen printing and ink-jet printing

    NASA Astrophysics Data System (ADS)

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

    1985-06-01

    Basic material efforts have proven to be very successful. Adherent and conductive films were achieved. A silver neodecanoate/bismuth 2-ethylhexanoate mixture has given the best results in both single and double layer applications. Another effort is continuing to examine the feasibility of applying metallo-organic deposition films by use of an ink jet printer. Direct line writing would result in a saving of process time and materials. So far, some well defined lines have been printed.

  10. Time-dependent dielectric breakdown measurements of porous organosilicate glass using mercury and solid metal probes

    SciTech Connect

    Pei, Dongfei; Nichols, Michael T.; Shohet, J. Leon; King, Sean W.; Clarke, James S.; Nishi, Yoshio

    2014-09-01

    Time-dependent dielectric breakdown (TDDB) is one of the major concerns for low-k dielectric materials. During plasma processing, low-k dielectrics are subjected to vacuum ultraviolet photon radiation and charged-particle bombardment. To examine the change of TDDB properties, time-to-breakdown measurements are made to porous SiCOH before and after plasma exposure. Significant discrepancies between mercury and solid-metal probes are observed and have been shown to be attributed to mercury diffusion into the dielectric porosities.

  11. Membranous glomerulonephropathy and nephrotic syndrome associated with iatrogenic metallic mercury poisoning in a cat.

    PubMed

    Shull, R M; Stowe, C M; Osborne, C A; O'Leary, T P; Vernier, R L; Hammer, R F

    1981-02-01

    The nephrotic syndrome, characterized by nonselective proteinuria, hypoproteinemia, hypoalbuminemia, and ascites, was observed in a 10-month-old male cat. Profound glomerular changes and renal tubular changes appear to have been induced by iatrogenic chronic exposure to metallic mercury originally contained in a rectal thermometer. Large concentrations of mercury were present in the kidneys, liver, spleen, and urine. Evaluation of glomeruli by immunofluorescent microscopy revealed interrupted granular deposition of immuno-globulin G and the third component of complement in glomerular capillary walls and the mesangium. Electron microscopic evaluation of glomeruli revealed diffuse alterations in glomerular basement membranes and visceral epithelial cells. Small electron dense deposits were observed in capillary walls, but they were not characteristic of immune complexes. The mechanism(s) responsible for the mercury induced glomerulonephropathy in this patient could not be determined on the basis of available data. PMID:7257162

  12. Cavitation-erosion resistance of 316LN stainless steel in mercury containing metallic solutes

    SciTech Connect

    Pawel, Steven J; Mansur, Louis K

    2003-01-01

    Room temperature cavitation tests of vacuum annealed type 316LN stainless steel were performed in pure mercury and in mercury with various amounts of metallic solute to evaluate potential mitigation of erosion/wastage. Tests were performed using an ultrasonic vibratory horn with specimens attached at the tip. All of the solutes examined, which included 5 wt% In, 10 wt% In, 4.4 wt% Cd, 2 wt% Ga, and a mixture that included 1 wt% each of Pb, Sn, and Zn, were found to increase cavitation-erosion as measured by increased weight loss and/or surface profile development compared to exposures for the same conditions in pure mercury. Qualitatively, each solute appeared to increase the tenacity of the post-test wetting of the Hg solutions and render the Hg mixture susceptible to manipulation of droplet shape. Published by Elsevier B.V.

  13. The influence of some relevant metallic impurities in the triple point of mercury temperature

    NASA Astrophysics Data System (ADS)

    Tabacaru, C.; del Campo, D.; Gómez, E.; García Izquiedo, C.; Welna, A.; Kalemci, M.; Pehlivan, Ö.

    2016-02-01

    The influence of impurities on the defined fixed points of the International Temperature Scale of 1990 is one of the most relevant sources of uncertainty in their use. Namely, the triple point of mercury is one of the fixed points most used because its assigned triple point temperature (-39,8344 °C) is within a temperature range of high interest for science and industry. Mercury can be obtained with high purity, usually better that 8N and it is realized with a high accuracy, what makes impurities a significant contributor on the final uncertainty. The best procedure to quantify this influence is by means of doping experiments which consist of the addition of a controlled amount of an impurity, determined gravimetrically, in a fixed point cell. This paper presents a summary of the results obtained from a series of doping experiments performed with some relevant metallic impurities on the triple point of mercury temperature.

  14. Occupational and Community Exposures to Toxic Metals: Lead, Cadmium, Mercury and Arsenic

    PubMed Central

    Landrigan, Philip J.

    1982-01-01

    Lead, cadmium, mercury and arsenic are widely dispersed in the environment. Adults are primarily exposed to these contaminants in the workplace. Children may be exposed to toxic metals from numerous sources, including contaminated air, water, soil and food. The chronic toxic effects of lead include anemia, neuropathy, chronic renal disease and reproductive impairment. Lead is a carcinogen in three animal species. Cadmium causes emphysema, chronic renal disease, cancer of the prostate and possibly of the lung. Inorganic mercury causes gingivitis, stomatitis, neurologic impairment and nephrosis, while organic mercurials cause sensory neuropathy, ataxia, dysarthria and blindness. Arsenic causes dermatitis, skin cancer, sensory neuropathy, cirrhosis, angiosarcoma of the liver, lung cancer and possibly lymphatic cancer. PMID:7164433

  15. Ink-jet printing of silver metallization for photovoltaics

    NASA Technical Reports Server (NTRS)

    Vest, R. W.

    1986-01-01

    The status of the ink-jet printing program at Purdue University is described. The drop-on-demand printing system was modified to use metallo-organic decomposition (MOD) inks. Also, an IBM AT computer was integrated into the ink-jet printer system to provide operational functions and contact pattern configuration. The integration of the ink-jet printing system, problems encountered, and solutions derived were described in detail. The status of ink-jet printing using a MOD ink was discussed. The ink contained silver neodecanate and bismuth 2-ethylhexanoate dissolved in toluene; the MOD ink decomposition products being 99 wt% AG, and 1 wt% Bi.

  16. Emergence of metallicity in silver clusters in the 150 atom regime: a study of differently sized silver clusters

    NASA Astrophysics Data System (ADS)

    Chakraborty, Indranath; Erusappan, Jayanthi; Govindarajan, Anuradha; Sugi, K. S.; Udayabhaskararao, Thumu; Ghosh, Atanu; Pradeep, Thalappil

    2014-06-01

    We report the systematic appearance of a plasmon-like optical absorption feature in silver clusters protected with 2-phenylethanethiol (PET), 4-flurothiophenol (4-FTP) and (4-(t-butyl)benzenethiol (BBS) as a function of cluster size. A wide range of clusters, namely, Ag44(4-FTP)30, Ag55(PET)31, ~Ag75(PET)40, ~Ag114(PET)46, Ag152(PET)60, ~Ag202(BBS)70, ~Ag423(PET)105, and ~Ag530(PET)100 were prepared. The UV/Vis spectra show multiple features up to ~Ag114 and thereafter, from Ag152 onwards, the plasmonic feature corresponding to a single peak at ~460 nm evolves, which points to the emergence of metallicity in clusters composed of ~150 metal atoms. A minor blue shift in the plasmonic peak was observed as cluster sizes increased and merged with the spectrum of plasmonic nanoparticles of 4.8 nm diameter protected with PET. Clusters with different ligands, such as 4-FTP and BBS, also show this behavior, which suggests that the `emergence of metallicity' is independent of the functionality of the thiol ligand.We report the systematic appearance of a plasmon-like optical absorption feature in silver clusters protected with 2-phenylethanethiol (PET), 4-flurothiophenol (4-FTP) and (4-(t-butyl)benzenethiol (BBS) as a function of cluster size. A wide range of clusters, namely, Ag44(4-FTP)30, Ag55(PET)31, ~Ag75(PET)40, ~Ag114(PET)46, Ag152(PET)60, ~Ag202(BBS)70, ~Ag423(PET)105, and ~Ag530(PET)100 were prepared. The UV/Vis spectra show multiple features up to ~Ag114 and thereafter, from Ag152 onwards, the plasmonic feature corresponding to a single peak at ~460 nm evolves, which points to the emergence of metallicity in clusters composed of ~150 metal atoms. A minor blue shift in the plasmonic peak was observed as cluster sizes increased and merged with the spectrum of plasmonic nanoparticles of 4.8 nm diameter protected with PET. Clusters with different ligands, such as 4-FTP and BBS, also show this behavior, which suggests that the `emergence of metallicity' is independent of

  17. 49 CFR 173.164 - Mercury (metallic and articles containing mercury).

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ...-specification reusable metal packagings. (e) Except for a hazardous substance or a hazardous waste or for... package does not exceed 1 g (0.035 ounce) are not subject to the requirements of this subchapter. (c..., leakproof and in sealed metal or plastic units. (2) Thermometers, switches and relays, each containing...

  18. Chromatic analysis by monitoring unmodified silver nanoparticles reduction on double layer microfluidic paper-based analytical devices for selective and sensitive determination of mercury(II).

    PubMed

    Meelapsom, Rattapol; Jarujamrus, Purim; Amatatongchai, Maliwan; Chairam, Sanoe; Kulsing, Chadin; Shen, Wei

    2016-08-01

    This study demonstrates chromatic analysis based on a simple red green blue (RGB) color model for sensitive and selective determination of mercury(II). The analysis was performed by monitoring the color change of a microfluidic Paper-based Analytical Device (µPAD). The device was fabricated by using alkyl ketene dimer (AKD)-inkjet printing and doped with unmodified silver nanoparticles (AgNPs) which were disintegrated when being exposed to mercury(II). The color intensity was detected by using an apparatus consisting of a digital camera and a homemade light box generating constant light intensity. A progressive increase in color intensity of the tested area on the µPAD (3.0mm) was observed with increasing mercury(II) concentration. The developed system enabled quantification of mercury(II) at low concentration with the detection limit of 0.001mgL(-1) (3 SD blank/slope of the calibration curve) and small sample volume uptake (2µL). The linearity range of the calibration curve in this technique was demonstrated from 0.05 to 7mgL(-1) (r(2)=0.998) with good precision (RSD less than 4.1%). Greater selectivity towards mercury(II) compared with potential interference ions was also observed. Furthermore, the percentage recoveries of spiked water samples were in an acceptable range which was in agreement with the values obtained from the conventional method utilizing cold vapor atomic absorption spectrometer (CVAAS). The proposed technique allows a rapid, simple, sensitive and selective analysis of trace mercury(II) in water samples. PMID:27216673

  19. The fate and transport of mercury, methylmercury, and other trace metals in Chesapeake Bay tributaries.

    PubMed

    Lawson, N M; Mason, R P; Laporte, J M

    2001-02-01

    Six tributaries to the Chesapeake Bay were analyzed for suspended particulate matter, dissolved organic carbon, particulate organic carbon, mercury, methylmercury, lead, nickel, zinc, cadmium, chromium, and copper. This study examined the importance of flow regime, suspended particulate concentration, and watershed characteristics on the transport of mercury, methylmercury, and other trace metals. Total mercury concentrations were higher under high flow conditions which is consistent with the tendency of this metal to bind strongly to particulate matter. Methylmercury showed less flow rate dependence. Nickel, lead, and zinc concentrations responded strongly to flow rate on the Potomac River, while weaker correlations were found on the other rivers sampled. Cadmium, copper, and chromium concentrations were the least influenced by flow. Partition coefficients calculated in this study were similar to those of other estuaries and overall decreased in the order of Hg > Ni-MMHg > Cr-Pb-Zn > Cd > Cu. Watershed yield estimates and associated retention factors were calculated for the various rivers. These calculations showed that for most of the rivers, mercury was the most strongly retained within the watershed. PMID:11229005

  20. Atomic-absorption determination of mercury in geological materials by flame and carbon-rod atomisation after solvent extraction and using co-extracted silver as a matrix modifier

    USGS Publications Warehouse

    Sanzolone, R.F.; Chao, T.T.

    1983-01-01

    Based on modifications and expansion of the original Tindall's solvent extraction flame atomic-absorption procedure, an atomic-absorption spectrophotometric method has been developed for the determination of mercury in geological materials. The sample is digested with nitric and hydrochloric acids in a boiling water-bath. The solution is made ammoniacal and potassium iodide and silver nitrate are added. The mercury is extracted into isobutyl methyl ketone as the tetraiodomercurate(ll). Added silver is co-extracted with mercury and serves as a matrix modifier in the carbon-rod atomiser. The mercury in the isobutyl methyl ketone extract may be determined by either the flame- or the carbon-rod atomisation method, depending on the concentration level. The limits of determination are 0.05-10 p.p.m. of mercury for the carbon-rod atomisation and 1 -200 p.p.m. of mercury for the flame atomisation. Mercury values for reference samples obtained by replicate analyses are in good agreement with those reported by other workers, with relative standard deviations ranging from 2.3 to 0.9%. Recoveries of mercury spiked at two levels were 93-106%. Major and trace elements commonly found in geological materials do not interfere.

  1. Anomalous concentrations of gold, silver, and other metals in the Mill Canyon area, Cortez quadrangle, Eureka and Lander Counties, Nevada

    USGS Publications Warehouse

    Elliott, James E.; Wells, John David

    1968-01-01

    The Mill Canyon area is in the eastern part of the Cortez window of the Roberts Mountains thrust belt in the Cortez quadrangle, north-central Nevada. Gold and silver ores have been mined from fissure veins in Jurassic quartz monzonite and in the bordering Wenban Limestone of Devonian age. Geochemical data show anomalies of gold, silver, lead, zinc, copper, arsenic, antimony, mercury, and tellurium. Geologic and geochemical studies indicate that a formation favorable for gold deposition, the Roberts Mountains Limestone of Silurian age, may be found at depth near the mouth of Mill Canyon.

  2. Self-encapsulated silver metallization and low-k polyimide for ultra-large-scale integration

    NASA Astrophysics Data System (ADS)

    Zou, Yuelin Lee

    An integrated approach has been taken to study the interconnect materials system and develop processes related to silver encapsulation, the metal dry etch, diffusion barrier and adhesion promoter, and low-dielectric-constant (low-k) polyimide materials. The objective is to develop a processing scheme for the low resistance metal and the low-k dielectrics, and to use fabricated test structures to demonstrate better performance especially in electromigration and dielectric insulation than the current industry standard for ultra-large-scale integration (ULSI) applications. Silver is an attractive choice of the low resistivity metal to replace aluminum alloy interconnect. A thin diffusion barrier for Ag metallization can be formed by nitridation of Ti using Ag/Ti bilayers in an ammonia ambient. A linear-parabolic model was proposed to describe the kinetics of the nitridation reaction. The Ti-nitride grows fast initially and a linear kinetics is presumed in a reaction-limiting step. After 15 min annealing, the nitride growth slows down and follows a parabolic growth kinetics. Silver films in Ag/Ti bilayer structures exhibited a strong < 111> texture component and a near-bamboo grain structures. In contrast, Ag films with randomly oriented grains were observed on Cr underlayers. The encapsulated silver layers had minimal residual Ti accumulations. X-ray analysis confirmed the absence of intermetallic phase transformation. Therefore, resistivity values of about 2 muOmega-cm were obtained for the encapsulated Ag bilayer films, which are comparable to that of the bulk values. A process was first reported to dry etch Ag metallization for microelectronic applications. Silver films oxidize readily in the oxygen plasma to form silver oxides, which subsequently crack and spall away due to incorporation of Ag to the oxide lattice. As a result, the oxide formed can be etched away in the reactive ion etch (RIE) chamber. The silver pattern prepared by the dry etching technique

  3. Mercury Induced by Pressure to act as a Transition Metal in Mercury Fluorides

    NASA Astrophysics Data System (ADS)

    Botana, Jorge; Wang, Xiaoli; Hou, Chunju; Yan, Dadong; Lin, Haiqing; Ma, Yanming; Miao, Mao-Sheng

    The question of whether Hg is a transition metal remains open for stable solids. In our work we propose that high-pressure techniques will help prepare unusual oxidation states of Hg in Hg-F compounds. By means of ab initio calculations and an advanced structure-search algorithm we find that under high pressure charge is transferred from the Hg d orbitals to the F, and becomes a transition metal. HgF3 and HgF4 have been found to be stable compounds at high pressure. HgF4 consists of planar molecules, a typical geometry for d8 metallic centers. HgF3 is an example of metallic and ferromagnetic compound, with an electronic structure analogous to transparent conductors due to the Hg d9 configuration.

  4. Strategies for specifically directing metal functionalization of protein nanotubes: constructing protein coated silver nanowires

    NASA Astrophysics Data System (ADS)

    Carreño-Fuentes, Liliana; Ascencio, Jorge A.; Medina, Ariosto; Aguila, Sergio; Palomares, Laura A.; Ramírez, Octavio T.

    2013-06-01

    Biological molecules that self-assemble in the nanoscale range are useful multifunctional materials. Rotavirus VP6 protein self-assembles into tubular structures in the absence of other rotavirus proteins. Here, we present strategies for selectively directing metal functionalization to the lumen of VP6 nanotubes. The specific in situ metal reduction in the inner surface of nanotube walls was achieved by the simple modification of a method previously reported to functionalize the nanotube outer surface. Silver nanorods and nanowires as long as 1.5 μm were formed inside the nanotubes by coalescence of nanoparticles. Such one-dimensional structures were longer than others previously obtained using bioscaffolds. The interactions between silver ions and the nanotube were simulated to understand the conditions that allowed nanowire formation. Molecular docking showed that a naturally occurring arrangement of aspartate residues enabled the stabilization of silver ions on the internal surface of the VP6 nanotubes. This is the first time that such a spatial arrangement has been proposed for the nucleation of silver nanoparticles, opening the possibility of using such an array to direct functionalization of other biomolecules. These results demonstrate the natural capabilities of VP6 nanotubes to function as a versatile biotemplate for nanomaterials.

  5. The formation of silver metal nanoparticles by ion implantation in silicate glasses

    NASA Astrophysics Data System (ADS)

    Vytykacova, S.; Svecova, B.; Nekvindova, P.; Spirkova, J.; Mackova, A.; Miksova, R.; Böttger, R.

    2016-03-01

    It has been shown that glasses containing silver metal nanoparticles are promising photonics materials for the fabrication of all-optical components. The resulting optical properties of the nanocomposite glasses depend on the composition and structure of the glass, as well as on the type of metal ion implanted and the experimental procedures involved. The main aim of this article was to study the influence of the conditions of the ion implantation and the composition of the glass on the formation of metal nanoparticles in such glasses. Four various types of silicate glasses were implanted with Ag+ ions with different energy (330 keV, 1.2 MeV and 1.7 MeV), with the fluence being kept constant (1 × 1016 ions cm-2). The as-implanted samples were annealed at 600 °C for 1 h. The samples were characterised in terms of: the nucleation of metal nanoparticles (linear optical absorption), the migration of silver through the glass matrix during the implantation and post-implantation annealing (Rutherford backscattering spectroscopy), and the oxidation state of silver (photoluminescence in the visible region).

  6. PHOTOPHORETIC SEPARATION OF METALS AND SILICATES: THE FORMATION OF MERCURY-LIKE PLANETS AND METAL DEPLETION IN CHONDRITES

    SciTech Connect

    Wurm, Gerhard; Trieloff, Mario; Rauer, Heike

    2013-05-20

    Mercury's high uncompressed mass density suggests that the planet is largely composed of iron, either bound within metal (mainly Fe-Ni) or iron sulfide. Recent results from the MESSENGER mission to Mercury imply a low temperature history of the planet which questions the standard formation models of impact mantle stripping or evaporation to explain the high metal content. Like Mercury, the two smallest extrasolar rocky planets with mass and size determination, CoRoT-7b and Kepler-10b, were found to be of high density. As they orbit close to their host stars, this indicates that iron-rich inner planets might not be a nuisance of the solar system but be part of a general scheme of planet formation. From undifferentiated chondrites, it is also known that the metal to silicate ratio is highly variable, which must be ascribed to preplanetary fractionation processes. Due to this fractionation, most chondritic parent bodies-most of them originated in the asteroid belt-are depleted in iron relative to average solar system abundances. The astrophysical processes leading to metal silicate fractionation in the solar nebula are essentially unknown. Here, we consider photophoretic forces. As these forces particularly act on irradiated solids, they might play a significant role in the composition of planetesimals forming at the inner edge of protoplanetary disks. Photophoresis can separate high thermal conductivity materials (iron) from lower thermal conductivity solids (silicate). We suggest that the silicates are preferentially pushed into the optically thick disk. Subsequent planetesimal formation at the edge moving outward leads to metal-rich planetesimals close to the star and metal depleted planetesimals farther out in the nebula.

  7. Interaction of gold, mercury, silver, and other ligands with selenium during oxidation of cysteine: relation to arthritis therapy

    SciTech Connect

    Dillard, C.J.; Tappel, A.; Tappel, A.L.

    1986-03-01

    Au, Ag, and Hg are soft-acid metal ligands for Se that inhibit Se-GSH peroxidase. A model system consisting of 100 ..mu..M cysteine, 10..mu..M selenocystine ((SeCys)/sub 2/), 100 ..mu..M acetate-1 mM EDTA buffer, pH 5.8, and various concentrations of metals was used to investigate Se-ligand interactions during 2 h incubations at 37/sup 0/C in an oxygen atmosphere. Cysteine was measured with 5,5'-dithiobis-(2-nitrobenzoic acid). Se-ligand interaction inhibits the catalytic effect of Se on cysteine oxidation. The k/sub i/ for inhibition of Se-catalyzed oxidation of cysteine was 0.13, 0.46, 1.6, and 1.3 ..mu..M HgCl/sub 3/, silver acetate, aurothioglucose, and aurothiomalate, respectively. Cadmium acetate, CdCl/sub 2/, and cis-platinum were weak inhibitors; zinc acetate and CuCl/sub 2/ were ineffective. Seleno-methionine did not catalyze cysteine oxidation, and Na/sub 2/SeO/sub 3/ was twice as effective as (SeCys)/sub 2/. Au inhibited the oxidation of CysSe/sup -/, produced by NaBH/sub 4/ reduction of (CysSe)/sub 2/, and its oxidation in oxygen was first-order. Au-compound inhibition of Se-catalyzed functions may have important implications in human rheumatoid patients during chrysotherapy.

  8. Heavy metal chelator TPEN attenuates fura-2 fluorescence changes induced by cadmium, mercury and methylmercury

    PubMed Central

    OHKUBO, Masato; MIYAMOTO, Atsushi; SHIRAISHI, Mitsuya

    2016-01-01

    Stimulation with heavy metals is known to induce calcium (Ca2+) mobilization in many cell types. Interference with the measurement of intracellular Ca2+ concentration by the heavy metals in cells loaded with Ca2+ indicator fura-2 is an ongoing problem. In this study, we analyzed the effect of heavy metals on the fura-2 fluorescence ratio in human SH-SY5Y neuroblastoma cells by using TPEN, a specific cell-permeable heavy metal chelator. Manganese chloride (30–300 µM) did not cause significant changes in the fura-2 fluorescence ratio. A high concentration (300 µM) of lead acetate induced a slight elevation in the fura-2 fluorescence ratio. In contrast, stimulation with cadmium chloride, mercury chloride or MeHg (3–30 µM) elicited an apparent elevation of the fura-2 fluorescence ratio in a dose-dependent manner. In cells stimulated with 10 or 30 µM cadmium chloride, the addition of TPEN decreased the elevated fura-2 fluorescence ratio to basal levels. In cells stimulated with mercury or MeHg, the addition of TPEN significantly decreased the elevation of the fura-2 fluorescence ratio induced by lower concentrations (10 µM) of mercury or MeHg, but not by higher concentrations (30 µM). Pretreatment with Ca2+ channel blockers, such as verapamil, 2-APB or lanthanum chloride, resulted in different effects on the fura-2 fluorescence ratio. Our study provides a characterization of the effects of several heavy metals on the mobilization of divalent cations and the toxicity of heavy metals to neuronal cells. PMID:26781706

  9. Heavy metal chelator TPEN attenuates fura-2 fluorescence changes induced by cadmium, mercury and methylmercury.

    PubMed

    Ohkubo, Masato; Miyamoto, Atsushi; Shiraishi, Mitsuya

    2016-06-01

    Stimulation with heavy metals is known to induce calcium (Ca(2+)) mobilization in many cell types. Interference with the measurement of intracellular Ca(2+) concentration by the heavy metals in cells loaded with Ca(2+) indicator fura-2 is an ongoing problem. In this study, we analyzed the effect of heavy metals on the fura-2 fluorescence ratio in human SH-SY5Y neuroblastoma cells by using TPEN, a specific cell-permeable heavy metal chelator. Manganese chloride (30-300 µM) did not cause significant changes in the fura-2 fluorescence ratio. A high concentration (300 µM) of lead acetate induced a slight elevation in the fura-2 fluorescence ratio. In contrast, stimulation with cadmium chloride, mercury chloride or MeHg (3-30 µM) elicited an apparent elevation of the fura-2 fluorescence ratio in a dose-dependent manner. In cells stimulated with 10 or 30 µM cadmium chloride, the addition of TPEN decreased the elevated fura-2 fluorescence ratio to basal levels. In cells stimulated with mercury or MeHg, the addition of TPEN significantly decreased the elevation of the fura-2 fluorescence ratio induced by lower concentrations (10 µM) of mercury or MeHg, but not by higher concentrations (30 µM). Pretreatment with Ca(2+) channel blockers, such as verapamil, 2-APB or lanthanum chloride, resulted in different effects on the fura-2 fluorescence ratio. Our study provides a characterization of the effects of several heavy metals on the mobilization of divalent cations and the toxicity of heavy metals to neuronal cells. PMID:26781706

  10. Thermal conductivity studies of novel nanofluids based on metallic silver decorated mesoporous silica nanoparticles

    SciTech Connect

    Tadjarodi, Azadeh; Zabihi, Fatemeh

    2013-10-15

    Graphical abstract: - Highlights: • Metallic silver was decorated in mSiO{sub 2} with grafted hemiaminal functional groups. • Synthesized nanoparticles were used for preparation of glycerol based nanofluids. • The effect of temperature, weight fraction of mSiO{sub 2} and concentration of silver nanoparticles on thermal conductivity of nanofluids was investigated. - Abstract: In the present study, the mesoporous structure of silica (mSiO{sub 2}) nanoparticles as well as hemiaminal grafted mSiO{sub 2} decorated by metallic silver (Ag/mSiO{sub 2}) has been used for the preparation of glycerol based nanofluids. Structural and morphological characterization of the synthesized products have been carried out using Fourier transform infrared spectroscopy (FTIR), scanning electron microscope (SEM), X-ray diffraction (XRD), UV–vis spectroscopy, inductively coupled plasma (ICP) and N{sub 2} adsorption–desorption isotherms. The thermal conductivity and viscosity of the nanofluids have been measured as a function of temperature for various weight fractions and silver concentrations of mSiO{sub 2} and Ag/mSiO{sub 2} nanoparticles, respectively. The results show that the thermal conductivity of the nanofluids increase up to 9.24% as the weight fraction of mSiO{sub 2} increases up to 4 wt%. Also, increasing the percent of the silver decorated mSiO{sub 2} (Ag/mSiO{sub 2}) up to 2.98% caused an enhancement in the thermal conductivity of the base fluid up to 10.95%. Furthermore, the results show that the nanofluids have Newtonian behavior in the tested temperature range for various concentrations of nanoparticles.

  11. Effects of Silver and Other Metals on the Cytoskeleton

    NASA Technical Reports Server (NTRS)

    Conrad, Gary W.

    1997-01-01

    Directly or indirectly, trace concentrations of silver ion (Ag(+)) stabilize microtubules (Conrad, A.H., et al. Cell Motil. & Cytoskel. 27:117-132), as does taxol (Conrad, A.H., et al. J. Exp. Zool. 262:154-165), an effect with major consequences for cellular shape changes and development. Polymerization of microtubules is gravity-sensitive (Tabony and Job, Proc. Natl. Acad. Sci. USA 89:6948-6952), so trace amounts of Ag(+) may alter cellular ability to respond to gravity. If Ag electrolysis is used to purify water on NASA space vehicles, plants and animals/astronauts will be exposed continuously to Ag(+), a regimen with unknown cellular and developmental consequences. Fertilized eggs of the marine mudsnail, Ilyanassa obsoleta, are the cells in which the effects of A(+) on microtubules were discovered. They distribute visible cytoplasmic contents according to gravity and contain cytoplasmic morphogenetic determinants for heart development. The objectives are to determine if the effects of Ag(+), AU(3+), (of biosensor relevance), or Gd(3+) (inhibitor of some stretch-activated ion channels) on the cytoskeleton (in the presence and absence of mechanical loading) will affect cellular responses to gravity.

  12. The effect and safety of dressing composed by nylon threads covered with metallic silver in wound treatment.

    PubMed

    Brogliato, Ariane R; Borges, Paula A; Barros, Janaina F; Lanzetti, Manuela; Valença, Samuel; Oliveira, Nesser C; Izário-Filho, Hélcio J; Benjamim, Claudia F

    2014-04-01

    Silver is used worldwide in dressings for wound management. Silver has demonstrated great efficacy against a broad range of microorganisms, but there is very little data about the systemic absorption and toxicity of silver in vivo. In this study, the antimicrobial effect of the silver-coated dressing (SilverCoat(®)) was evaluated in vitro against the most common microorganisms found in wounds, including Pseudomonas aeruginosa, Candida albicans, Staphylococcus aureus, Methicillin-resistant Staphylococcus aureus and Klebsiella pneumoniae. We also performed an excisional skin lesion assay in mice to evaluate wound healing after 14 days of treatment with a silver-coated dressing, and we measured the amount of silver in the blood, the kidneys and the liver after treatment. Our data demonstrated that the nylon threads coated with metallic silver have a satisfactory antimicrobial effect in vitro, and the prolonged use of these threads did not lead to systemic silver absorption, did not induce toxicity in the kidneys and the liver and were not detrimental to the normal wound-healing process. PMID:22905783

  13. Compatibility Study of Silver Biocide in Drinking Water with Candidate Metals for Crew Exploration Vehicle Potable Water System

    NASA Technical Reports Server (NTRS)

    Adam, Niklas M.

    2009-01-01

    The stability of silver biocide, used to keep drinking water on the CEV potable water sterile, is unknown as the system design is still in progress. Silver biocide in water can deplete rapidly when exposed to various metal surfaces. Additionally, silver depletion rates may be affected by the surface-area-to-volume (SA/V) ratios in the water system. Therefore, to facilitate the CEV water system design, it would be advantageous to know the biocide depletion rates in water exposed to the surfaces of these candidate metals at various SA/V ratios. Certain surface treatments can be employed to reduce the depletion rates of silver compared to the base metal. The purpose of this work is to determine the compatibility of specific spaceflight-certified metals that could used in the design of the CEV potable water system with silver biocide as well as understand the effect of surface are to volume ratios of metals used in the construction of the potable water system on the silver concentration.

  14. Pollution by Arsenic, Mercury and other Heavy Metals in Sunchulli mining district of Apolobamba (Bolivia)

    NASA Astrophysics Data System (ADS)

    Terán Mita, Tania; Faz Cano, Angel; Muñoz, Maria Angeles; Millán Gómez, Rocio; Chincheros Paniagua, Jaime

    2010-05-01

    In Bolivia, metal mining activities since historical times have been one of the most important sources of environmental pollution. This is the case of the National Area of Apolobamba Integrated Management (ANMIN of Apolobamba) in La Paz, Bolivia, where intense gold mining activities have been carried out from former times to the present, with very little gold extraction and very primitive mineral processing technology; in fact, mercury is still being used in the amalgam processes of the gold concentration, which is burned outdoors to recover the gold. Sunchullí is a representative mining district in ANMIN of Apolobamba where mining activity is mainly gold extraction and its water effluents go to the Amazonian basin; in this mining district the productivity of extracted mineral is very low but the processes can result in heavy-metal contamination of the air, water, soils and plants. Due to its high toxicity, the contamination by arsenic and mercury create the most critical environmental problems. In addition, some other heavy metals may also be present such as lead, copper, zinc and cadmium. These heavy metals could be incorporated in the trophic chain, through the flora and the fauna, in their bio-available and soluble forms. Inhabitants of this area consume foodcrops, fish from lakes and rivers and use the waters for the livestock, domestic use, and irrigation. The aim of this work was to evaluate the heavy metals pollution by gold mining activities in Sunchullí area. In Sunchullí two representative zones were distinguished and sampled. Zone near the mining operation site was considered as affected by mineral extraction processes, while far away zones represented the non affected ones by the mining operation. In each zone, 3 plots were established; in each plot, 3 soil sampling points were selected in a random manner and analysed separately. In each sampling point, two samples were taken, one at the surface, from 0-5 cm depth (topsoil), and the other between 5

  15. The role of mercury and cadmium heavy metals in vascular disease, hypertension, coronary heart disease, and myocardial infarction.

    PubMed

    Houston, Mark C

    2007-01-01

    Mercury, cadmium, and other heavy metals have a high affinity for sulfhydryl (-SH) groups, inactivating numerous enzymatic reactions, amino acids, and sulfur-containing antioxidants (NAC, ALA, GSH), with subsequent decreased oxidant defense and increased oxidative stress. Both bind to metallothionein and substitute for zinc, copper, and other trace metals reducing the effectiveness of metalloenzymes. Mercury induces mitochondrial dysfunction with reduction in ATP, depletion of glutathione, and increased lipid peroxidation; increased oxidative stress is common. Selenium antagonizes mercury toxicity. The overall vascular effects of mercury include oxidative stress, inflammation, thrombosis, vascular smooth muscle dysfunction, endothelial dysfunction, dyslipidemia, immune dysfunction, and mitochondrial dysfunction. The clinical consequences of mercury toxicity include hypertension, CHD, MI, increased carotid IMT and obstruction, CVA, generalized atherosclerosis, and renal dysfunction with proteinuria. Pathological, biochemical, and functional medicine correlations are significant and logical. Mercury diminishes the protective effect of fish and omega-3 fatty acids. Mercury, cadmium, and other heavy metals inactivate COMT, which increases serum and urinary epinephrine, norepinephrine, and dopamine. This effect will increase blood pressure and may be a clinical clue to heavy metal toxicity. Cadmium concentrates in the kidney, particularly inducing proteinuria and renal dysfunction; it is associated with hypertension, but less so with CHD. Renal cadmium reduces CYP4A11 and PPARs, which may be related to hypertension, sodium retention, glucose intolerance, dyslipidemia, and zinc deficiency. Dietary calcium may mitigate some of the toxicity of cadmium. Heavy metal toxicity, especially mercury and cadmium, should be evaluated in any patient with hypertension, CHD, or other vascular disease. Specific testing for acute and chronic toxicity and total body burden using hair

  16. Selective colorimetric sensors based on the monitoring of an unmodified silver nanoparticles (AgNPs) reduction for a simple and rapid determination of mercury

    NASA Astrophysics Data System (ADS)

    Jarujamrus, Purim; Amatatongchai, Maliwan; Thima, Araya; Khongrangdee, Thatsanee; Mongkontong, Chakrit

    2015-05-01

    In this work, selective colorimetric sensors for simple and rapid detection of Hg(II) ions based on the monitoring of an unmodified silver nanoparticles (AgNPs) reduction were developed. The average diameter of synthesized AgNPs was 8.3 ± 1.4 nm which was characterized by transmission electron microscopy (TEM). The abrupt change in absorbance of the unmodified AgNPs was observed which progressively decreased and slightly shifted to the blue wavelength as the concentration of Hg(II) increased, indicating the oxidation of Ag(0) to Ag(I) occurred. It appears that the AgNPs were oxidized by Hg(II), resulting in disintegration of the AgNPs into smaller particles as well as mediating the reduction of Hg(II) to Hg(0) adsorbed onto the surface of AgNPs. The adsorption of Hg(0) resulted in the lack of sufficient charges on AgNPs surfaces due to the decrease in the surface coverage of negatively charged citrate molecules, which then leaded to enlargement of AgNPs. The calibration curve of this technique was demonstrated from 0.5 to 7 ppm (r2 = 0.995), the limit of detection (LOD) was 0.06 ppm (SDblank/slope of calibration curve) with the precision (RSD, n = 4) of 3.24-4.53. Interestingly, the results show a significant enhance in the Hg(II) analytical sensitivity when Cu(II) is doped onto the unmodified AgNPs, which improves the quantitative detection limit to 0.008 ppm. In addition, greater selectivity toward Hg(II) compared with the other metal ions tested was observed. Furthermore, the percentage recoveries of spiked drinking water, tap water and SRM1641d (mercury in water) were in acceptable range with a good precision (RSD) which were in agreement with the values obtained from graphite furnace atomic absorption spectrometer (GFAAS). The technique proposed in this study provides a rapid, simple, sensitive and selective detection method for Hg(II) in water samples.

  17. Atmospheric mercury emissions from China's primary nonferrous metal (Zn, Pb and Cu) smelting during 1949-2010

    NASA Astrophysics Data System (ADS)

    Ye, Xuejie; Hu, Dan; Wang, Huanhuan; Chen, Long; Xie, Han; Zhang, Wei; Deng, Chunyan; Wang, Xuejun

    2015-02-01

    Primary nonferrous metal smelting is one of the most significant anthropogenic mercury emission sources. A spatially resolved mercury emission inventory over a long time span is essential for assessment of mercury source attribution and mercury transport modeling. In this study, based on updated technology-based emission factors, the atmospheric mercury emissions originating from primary zinc, lead and copper smelting in China were calculated. The inventory indicated that the total mercury emission from nonferrous metal smelting in China was 14.65 Mg in 2010, lower than the estimations in previous studies. The contributions of point and non-point sources were 23.3% and 76.7%, respectively. In 2010, the mercury emission from primary zinc, lead and copper smelting was 7.49, 6.05 and 1.10 Mg, respectively, and the Hg2+, Hg0 and HgP emissions were 8.10, 6.16 and 0.75 Mg, respectively. Spatially, the province with the largest emission was Sichuan, followed by Henan, Gansu, Shaanxi, Hunan and Yunnan provinces. The historical emissions were estimated based on dynamic emission factors that take the temporal technology changes into consideration. During 1949-2010, the cumulative mercury emission from China's nonferrous metal smelting was 323.0 Mg, of which the emission from lead smelting accounted for 44.6%, followed by zinc smelting (32.8%) and copper smelting (22.6%). From 1949 to 2010, the contribution of mercury emission from zinc smelting increased from 1.4% to 53.7%, while that from lead smelting showed a decreasing trend. For copper smelting, its contribution reached the maximum (40.1%) in 1987.

  18. Silver nanoparticles enhanced multichannel transition luminescence of Pr3+ in heavy metal germanium tellurite glasses

    NASA Astrophysics Data System (ADS)

    Du, Y. Y.; Chen, B. J.; Pun, E. Y. B.; Wang, Z. Q.; Zhao, X.; Lin, H.

    2015-01-01

    Enhanced luminescence of Pr3+ was observed in heavy metal germanium tellurite (NZPGT) glasses containing silver nanoparticles. Long-time annealing at 300 °C yield spherical and well-dispersed Ag nanoparticles with ~4 nm diameter as evidenced by transmission electron microscope (TEM). Multichannel transition luminescence intensity of Pr3+ in Ag nanoparticles embedded glasses grows by ~36% in comparison with the glasses without silver doping, which provides a new approach to improve energy conversion efficiency of GaAsAl solar cells. Hypersensitive probe Eu3+ reveals that electric field around rare-earth ions is remarkably enhanced due to the presence of Ag nanoparticles in the glass matrix, resulting in the luminescence intensification of Pr3+ in NZPGT glasses embedded with Ag nanoparticles.

  19. Mercury toxicity and neurodegenerative effects.

    PubMed

    Carocci, Alessia; Rovito, Nicola; Sinicropi, Maria Stefania; Genchi, Giuseppe

    2014-01-01

    Mercury is among the most toxic heavy metals and has no known physiological role in humans. Three forms of mercury exist: elemental, inorganic and organic. Mercury has been used by man since ancient times. Among the earliest were the Chinese and Romans, who employed cinnabar (mercury sulfide) as a red dye in ink (Clarkson et al. 2007). Mercury has also been used to purify gold and silver minerals by forming amalgams. This is a hazardous practice, but is still widespread in Brazil's Amazon basin, in Laos and in Venezuela, where tens of thousands of miners are engaged in local mining activities to find and purify gold or silver. Mercury compounds were long used to treat syphilis and the element is still used as an antiseptic,as a medicinal preservative and as a fungicide. Dental amalgams, which contain about 50% mercury, have been used to repair dental caries in the U.S. since 1856.Mercury still exists in many common household products around the world.Examples are: thermometers, barometers, batteries, and light bulbs (Swain et al.2007). In small amounts, some organo mercury-compounds (e.g., ethylmercury tiosalicylate(thimerosal) and phenylmercury nitrate) are used as preservatives in some medicines and vaccines (Ballet al. 2001).Each mercury form has its own toxicity profile. Exposure to Hg0 vapor and MeHg produce symptoms in CNS, whereas, the kidney is the target organ when exposures to the mono- and di-valent salts of mercury (Hg+ and Hg++, respectively)occur. Chronic exposure to inorganic mercury produces stomatitis, erethism and tremors. Chronic MeHg exposure induced symptoms similar to those observed in ALS, such as the early onset of hind limb weakness (Johnson and Atchison 2009).Among the organic mercury compounds, MeHg is the most biologically available and toxic (Scheuhammer et a!. 2007). MeHg is neurotoxic, reaching high levels of accumulation in the CNS; it can impair physiological function by disrupting endocrine glands (Tan et a!. 2009).The most

  20. Mercury contamination in agricultural soils from abandoned metal mines classified by geology and mineralization.

    PubMed

    Kim, Han Sik; Jung, Myung Chae

    2012-01-01

    This survey aimed to compare mercury concentrations in soils related to geology and mineralization types of mines. A total of 16,386 surface soils (0~15 cm in depth) were taken from agricultural lands near 343 abandoned mines (within 2 km from each mine) and analyzed for Hg by AAS with a hydride-generation device. To meaningfully compare mercury levels in soils with geology and mineralization types, three subclassification criteria were adapted: (1) five mineralization types, (2) four valuable ore mineral types, and (3) four parent rock types. The average concentration of Hg in all soils was 0.204 mg kg(-1) with a range of 0.002-24.07 mg kg(-1). Based on the mineralization types, average Hg concentrations (mg kg(-1)) in the soils decreased in the order of pegmatite (0.250) > hydrothermal vein (0.208) > hydrothermal replacement (0.166) > skarn (0.121) > sedimentary deposits (0.045). In terms of the valuable ore mineral types, the concentrations decreased in the order of Au-Ag-base metal mines ≈ base metal mines > Au-Ag mines > Sn-W-Mo-Fe-Mn mines. For parent rock types, similar concentrations were found in the soils derived from sedimentary rocks and metamorphic rocks followed by heterogeneous rocks with igneous and metamorphic processes. Furthermore, farmland soils contained relatively higher Hg levels than paddy soils. Therefore, it can be concluded that soils in Au, Ag, and base metal mines derived from a hydrothermal vein type of metamorphic rocks and pegmatite deposits contained relatively higher concentrations of mercury in the surface environment. PMID:21814815

  1. Bio-functionalized silver nanoparticles for selective colorimetric sensing of toxic metal ions and antimicrobial studies.

    PubMed

    Vinod Kumar, V; Anbarasan, S; Christena, Lawrence Rene; SaiSubramanian, Nagarajan; Philip Anthony, Savarimuthu

    2014-08-14

    Hibiscus Sabdariffa (Gongura) plant extracts (leaves (HL) and stem (HS)) were used for the first time in the green synthesis of bio-functionalized silver nanoparticles (AgNPs). The bio-functionality of AgNPs has been successfully utilized for selective colorimetric sensing of potentially health and environmentally hazardous Hg(2+), Cd(2+) and Pb(2+) metal ions at ppm level in aqueous solution. Importantly, clearly distinguishable colour for all three metal ions was observed. The influence of extract preparation condition and pH were also explored on the formation of AgNPs. Both selectivity and sensitivity differed for AgNPs synthesized from different parts of the plant. Direct correlation between the stability of green synthesized AgNPs at different pH and its antibacterial effects has been established. The selective colorimetric sensing of toxic metal ions and antimicrobial effect of green synthesized AgNPs demonstrated the multifunctional applications of green nanotechnology. PMID:24717716

  2. Bio-functionalized silver nanoparticles for selective colorimetric sensing of toxic metal ions and antimicrobial studies

    NASA Astrophysics Data System (ADS)

    Vinod Kumar, V.; Anbarasan, S.; Christena, Lawrence Rene; SaiSubramanian, Nagarajan; Philip Anthony, Savarimuthu

    2014-08-01

    Hibiscus Sabdariffa (Gongura) plant extracts (leaves (HL) and stem (HS) were used for the first time in the green synthesis of bio-functionalized silver nanoparticles (AgNPs). The bio-functionality of AgNPs has been successfully utilized for selective colorimetric sensing of potentially health and environmentally hazardous Hg2+, Cd2+ and Pb2+ metal ions at ppm level in aqueous solution. Importantly, clearly distinguishable colour for all three metal ions was observed. The influence of extract preparation condition and pH were also explored on the formation of AgNPs. Both selectivity and sensitivity differed for AgNPs synthesized from different parts of the plant. Direct correlation between the stability of green synthesized AgNPs at different pH and its antibacterial effects has been established. The selective colorimetric sensing of toxic metal ions and antimicrobial effect of green synthesized AgNPs demonstrated the multifunctional applications of green nanotechnology.

  3. Recovery of mercury from acid waste residues

    DOEpatents

    Greenhalgh, W.O.

    1987-02-27

    Mercury can be recovered from nitric acid-containing fluids by reacting the fluid with aluminum metal to produce mercury metal, and thence quenching the reactivity of the nitric acid prior to nitration of the mercury metal. 1 fig.

  4. Recovery of mercury from acid waste residues

    DOEpatents

    Greenhalgh, Wilbur O.

    1989-01-01

    Mercury can be recovered from nitric acid-containing fluids by reacting the fluid with aluminum metal to produce mercury metal, and then quenching the reactivity of the nitric acid prior to nitration of the mercury metal.

  5. Recovery of mercury from acid waste residues

    DOEpatents

    Greenhalgh, Wilbur O.

    1989-12-05

    Mercury can be recovered from nitric acid-containing fluids by reacting the fluid with aluminum metal to produce mercury metal, and then quenching the reactivity of the nitric acid prior to nitration of the mercury metal.

  6. Contact resistivity decrease at a metal/semiconductor interface by a solid-to-liquid phase transitional metallo-organic silver.

    PubMed

    Shin, Dong-Youn; Seo, Jun-Young; Kang, Min Gu; Song, Hee-eun

    2014-09-24

    We present a new approach to ensure the low contact resistivity of a silver paste at a metal/semiconductor interface over a broad range of peak firing temperatures by using a solid-to-liquid phase transitional metallo-organic silver, that is, silver neodecanoate. Silver nanoclusters, thermally derived from silver neodecanoate, are readily dissolved into the melt of metal oxide glass frit even at low temperatures, at which point the molten metal oxide glass frit lacks the dissociation capability of bulk silver into Ag(+) ions. In the presence of O(2-) ions in the melt of metal oxide glass frit, the redox reaction from Ag(+) to Ag(0) augments the noble-metal-assisted etching capability to remove the passivation layer of silicon nitride. Moreover, during the cooling stage, the nucleated silver atoms enrich the content of silver nanocolloids in the solidified metal oxide glass layer. The resulting contact resistivity of silver paste with silver neodecanoate at the metal/semiconductor interface thus remains low-between 4.12 and 16.08 mΩ cm(2)-whereas without silver neodecanoate, the paste exhibits a contact resistivity between 2.61 and 72.38 mΩ cm(2) in the range of peak firing temperatures from 750 to 810 °C. The advantage of using silver neodecanoate in silver paste becomes evident in that contact resistivity remains low over the broad range of peak firing temperatures, thus providing greater flexibility with respect to the firing temperature required in silicon solar cell applications. PMID:25182502

  7. Effect of chlorine in clay-mineral specimens prepared on silver metal-membrane mounts for X-ray powder diffraction analysis

    USGS Publications Warehouse

    Poppe, L.J.; Commeau, J.A.; Pense, G.M.

    1989-01-01

    Silver metal-membrane filters are commonly used as substrates in the preparation of oriented clay-mineral specimens for X-ray powder diffraction (XRD). The silver metal-membrane filters, however, present some problems after heat treatment if either the filters or the samples contain significant amounts of chlorine. At elevated temperature, the chloride ions react with the silver substrate to form crystalline compounds. These compounds change the mass-absorption coefficient of the sample, reducing peak intensities and areas and, therefore, complicating the semiquantitative estimation of clay minerals. A simple procedure that eliminates most of the chloride from a sample and the silver metal-membrane substrate is presented here.

  8. Got Mercury?

    NASA Technical Reports Server (NTRS)

    Meyers, Valerie E.; McCoy, J. Torin; Garcia, Hector D.; James, John T.

    2009-01-01

    Many of the operational and payload lighting units used in various spacecraft contain elemental mercury. If these devices were damaged on-orbit, elemental mercury could be released into the cabin. Although there are plans to replace operational units with alternate light sources, such as LEDs, that do not contain mercury, mercury-containing lamps efficiently produce high quality illumination and may never be completely replaced on orbit. Therefore, exposure to elemental mercury during spaceflight will remain possible and represents a toxicological hazard. Elemental mercury is a liquid metal that vaporizes slowly at room temperature. However, it may be completely vaporized at the elevated operating temperatures of lamps. Although liquid mercury is not readily absorbed through the skin or digestive tract, mercury vapors are efficiently absorbed through the respiratory tract. Therefore, the amount of mercury in the vapor form must be estimated. For mercury releases from lamps that are not being operated, we utilized a study conducted by the New Jersey Department of Environmental Quality to calculate the amount of mercury vapor expected to form over a 2-week period. For longer missions and for mercury releases occurring when lamps are operating, we conservatively assumed complete volatilization of the available mercury. Because current spacecraft environmental control systems are unable to remove mercury vapors, both short-term and long-term exposures to mercury vapors are possible. Acute exposure to high concentrations of mercury vapors can cause irritation of the respiratory tract and behavioral symptoms, such as irritability and hyperactivity. Chronic exposure can result in damage to the nervous system (tremors, memory loss, insomnia, etc.) and kidneys (proteinurea). Therefore, the JSC Toxicology Group recommends that stringent safety controls and verifications (vibrational testing, etc.) be applied to any hardware that contains elemental mercury that could yield

  9. Structure, dynamic and energetic of mixed transition metal clusters. A computational study of mixed clusters of silver and nickel

    NASA Astrophysics Data System (ADS)

    Hewage, J. W.; Rupika, W. L.; Amar, F. G.

    2012-11-01

    Classical molecular dynamics simulation (MD) with Sutton-Chen potential has been used to generate the minimum energy and to study the thermodynamic and dynamic properties of mixed transition metal cluster motifs of Ag n Ni(13- n) for n ≤ 13. Literature results of thirteen particle clusters of neat silver and nickel atoms were first reproduced before the successive replacement of the silver atom by nickel. Calculation was repeated for both silver-centred and nickel-centred clusters. It was found that the nickel-centred clusters were more stable than the silver-centred clusters. Heat capacities and hence the melting points of silver and nickel-centred clusters were determined by using the Histogram method. Species-centric order parameters developed by Hewage and Amar were used to understand the dynamic behaviour in the transition of silver-centred clusters to more stable nickel-centred clusters. This species-centric order parameter calculation further confirmed the stability of nickel-centred clusters over those of silver-centred species.

  10. Predicted energy densitites for nickel-hydrogen and silver-hydrogen cells embodying metallic hydrides for hydrogen storage

    NASA Technical Reports Server (NTRS)

    Easter, R. W.

    1974-01-01

    Simplified design concepts were used to estimate gravimetric and volumetric energy densities for metal hydrogen battery cells for assessing the characteristics of cells containing metal hydrides as compared to gaseous storage cells, and for comparing nickel cathode and silver cathode systems. The silver cathode was found to yield superior energy densities in all cases considered. The inclusion of hydride forming materials yields cells with very high volumetric energy densities that also retain gravimetric energy densities nearly as high as those of gaseous storage cells.

  11. Determination of mercurous chloride and total mercury in mercury ores

    USGS Publications Warehouse

    Fahey, J.J.

    1937-01-01

    A method for the determination of mercurous chloride and total mercury on the same sample is described. The mercury minerals are volatilized in a glass tube and brought into intimate contact with granulated sodium carbonate. The chlorine is fixed as sodium chloride, determined with silver nitrate, and computed to mercurous chloride. The mercury is collected on a previously weighed gold coil and weighed.

  12. Morphological evolution of silver nanoparticles and its effect on metal-induced chemical etching of silicon.

    PubMed

    Baek, Seong-Ho; Kong, Bo Hyun; Cho, Hyung Koun; Kim, Jae Hyun

    2013-05-01

    In this report, we have demonstrated the morphological evolution of the silver nanoparticles (AgNPs) by controlling the growth conditions and its effect on morphology of silicon (Si) during metal-induced electroless etching (MICE). Self-organized AgNPs with peculiarly shape were synthesized by an electroless plating method in a conventional aqueous hydrofluoric acid (HF) and silver nitrate (AgNO3) solution. AgNP nuclei were densely created on Si wafer surface, and they had a strong tendency to merge and form continuous metal films with increasing AgNO3 concentrations. Also, we have demonstrated that the fabrication of aligned Si nanowire (SiNW) arrays in large area of p-Si (111) substrates by MICE in a mixture of HF and hydrogen peroxide (H2O2) solution. We have found that the morphology of the initial AgNPs and oxidant concentration (H2O2) greatly influence on the shape of the SiNW etching profile. The morphological results showed that AgNP shapes were closely related to the etching direction of SiNWs, that is, the spherical AgNPs preferred to move vertical to the Si substrate, whereas non-spherical AgNPs changed their movement to the [100] directions. In addition, as the etching activity was increased at higher H2O2 concentrations, AgNPs had a tendency to move from the original [111] direction to the energetically preferred [100] direction. PMID:23858934

  13. Release of the self-quenching of fluorescence near silver metallic surfaces.

    PubMed

    Lakowicz, Joseph R; Malicka, Joanna; D'Auria, Sabato; Gryczynski, Ignacy

    2003-09-01

    Fluorescein is one of the most widely used fluorescent probes in microscopy, biotechnology, and clinical assays. One difficulty with fluorescein is its self-quenching, which results in decreased intensities with increasing labeling density. In this study we examined human serum albumin (HSA), which contained one to nine covalently linked fluorescein molecules per molecule of HSA. The occurrence of homo resonance energy transfer for labeling ratios greater than 1 were confirmed by decreases in the relative quantum yields, anisotropies, and lifetimes. We found that most of the self-quenching can be partially eliminated by proximity of the labeled protein to metallic silver particles. These results suggest the use of heavily labeled proteins and metallic colloids to obtain ultrabright reagents for use in immunoassays, imaging, and other applications. PMID:12895465

  14. Metals, Oxidative Stress and Neurodegeneration: A focus on Iron, Manganese and Mercury

    PubMed Central

    Farina, Marcelo; Avila, Daiana Silva; da Rocha, João Batista Teixeira

    2013-01-01

    Essential metals are crucial for the maintenance of cell homeostasis. Among the 23 elements that have known physiological functions in humans, 12 are metals, including iron (Fe) and manganese (Mn). Nevertheless, excessive exposure to these metals may lead to pathological conditions, including neurodegeneration. Similarly, exposure to metals that do not have known biological functions, such as mercury (Hg), also present great health concerns. This reviews focuses on the neurodegenerative mechanisms and effects of Fe, Mn and Hg. Oxidative stress (OS), particularly in mitochondria, is a common feature of Fe, Mn and Hg toxicity. However, the primary molecular targets triggering OS are distinct. Free cationic iron is a potent pro-oxidant and can initiate a set of reactions that form extremely reactive products, such as OH•. Mn can oxidize dopamine (DA), generating reactive species and also affect mitochondrial function, leading to accumulation of metabolites and culminating with OS. Cationic Hg forms have strong affinity for nucleophiles, such as –SH and –SeH. Therefore, they target critical thiol- and selenol-molecules with antioxidant properties. Finally, we address the main sources of exposure to these metals, their transport mechanisms into the brain, and therapeutic modalities to mitigate their neurotoxic effects. PMID:23266600

  15. Effect of heavy metals on the stabilization of mercury(II) by DTCR in desulfurization solutions.

    PubMed

    Hou, Jiaai; Lu, Rongjie; Sun, Mingyang; Baig, Shams Ali; Tang, Tingmei; Cheng, Lihua; Xu, Xinhua

    2012-05-30

    Several heavy metals, including Cu(2+), Ni(2+), Pb(2+), and Zn(2+), were investigated in simulated desulfurization solutions to evaluate their interferences with Hg(2+) during the reaction with dithiocarbamate type chelating resin (DTCR). Appropriate DTCR dosage and the effect of pH were also explored with respect to restoration of high Hg(2+) precipitation efficiency and reduction of mercury concentrations. The experimental results suggested that increasing heavy metal concentration inhibited Hg(2+) precipitation efficiency to a considerable extent and the inhibition order of the four heavy metals was Cu(2+)>Ni(2+)>Pb(2+)>Zn(2+). However, the coordination ability was closely related to the configuration and the orbital hybridization of each metal. In the cases of Cu(2+) and Pb(2+), increased DTCR dosage was beneficial to Hg(2+) precipitation, which could lay the foundation of practical applications of DTCR dosage for industrial wastewater treatment. The enhanced Hg(2+) precipitation performance seen for increasing pH might have come from the deprotonation of sulfur atoms on the DTCR functional groups and the formation of metal hydroxides (M(OH)(2), M=Cu, Pb, Hg). PMID:22469431

  16. Mercury and trace metal partitioning and fluxes in suburban Southwest Ohio watersheds.

    PubMed

    Naik, Avani P; Hammerschmidt, Chad R

    2011-10-15

    Many natural watersheds are increasingly affected by changes in land use associated with suburban sprawl and such alterations may influence concentrations, partitioning, and fluxes of toxic trace metals in fluvial ecosystems. We investigated the cycling of mercury (Hg), monomethylmercury, cadmium, copper, lead, nickel, and zinc in three watersheds at the urban fringe of Dayton, Ohio, over a 13-month period. Metal concentrations were related positively to discharge in each stream, with each metal having a high affinity for suspended particles and Hg also having a noticeable association with dissolved organic carbon. Although not observed for the other metals, levels of Hg in river water varied seasonally and among streams. Yields of Hg from two of the catchments were comparable to that predicted for runoff of atmospherically deposited Hg (∼25% of wet atmospheric flux), whereas the third watershed had a significantly greater annual flux associated with greater particle-specific and filtered water Hg concentrations, presumably from a point source. Fluxes of metals other than Hg were similar among each watershed and suggestive of a ubiquitous source, which could be either atmospheric deposition or weathering. Results of this study indicate that, with the exception of Hg being increased in one watershed, processes affecting metal partitioning and loadings are similar among southwest Ohio streams and comparable to other North American rivers that are equally or less impacted by urban development. Relative differences in land use, catchment area, and presence or absence of waste water treatment facilities had little or no detectable effect on most trace metal concentrations and fluxes. This suggests that suburban encroachment on agricultural and undeveloped lands has either similarly or not substantially impacted trace metal cycling in streams at the urban fringe of Dayton and, by extension, other comparable metropolitan areas. PMID:21827962

  17. Geochemistry, geochronology, mineralogy, and geology suggest sources of and controls on mineral systems in the southern Toquima Range, Nye County, Nevada; with geochemistry maps of gold, silver, mercury, arsenic, antimony, zinc, copper, lead, molybdenum, bismuth, iron, titanium, vanadium, cobalt, beryllium, boron, fluorine, and sulfur; and with a section on lead associations, mineralogy and paragenesis, and isotopes

    USGS Publications Warehouse

    Shawe, Daniel R.; Hoffman, James D.; Doe, Bruce R.; Foord, Eugene E.; Stein, Holly J.; Ayuso, Robert A.

    2003-01-01

    distribution patterns that suggest specific sources and lithologic influences on deposition, as well as multiple episodes of mineralization. Principal episodes of mineralization are Late Cretaceous (molybdenum and tungsten in and near granite; silver at Belmont and Silver Point mines), early Oligocene [tourmaline and base- and precious-metals around the granodiorite of Dry Canyon stock as well as at Manhattan(?)], late Oligocene (gold at Round Mountain and Jefferson), and Miocene (gold at Manhattan). Most likely principal sources of molybdenum, tungsten, silver, and bismuth are Cretaceous granites; of antimony, arsenic, and mercury are intermediate-composition early Oligocene intrusives; and of gold are early and late Oligocene and early Miocene magmas of the volcanic cycle. Lead may have been derived principally from Cretaceous granitic magma and Paleozoic sedimentary rocks. Several areas prospective for undiscovered mineral deposits are suggested by spatial patterns of element distributions related to geologic features. The Manhattan district in the vicinity of the White Caps mine may be underlain by a copper-molybdenum porphyry system related to a buried stock; peripheral high-grade gold veins and skarn deposits may be present below deposits previously mined. The Jefferson district also may be underlain by a copper-molybdenum porphyry system related to a buried stock, it too with peripheral high-grade gold deposits. The Bald Mountain Canyon belt of small gold veins has potential for deeper deposits in buried porous ash-flow tuff similar to the huge Round Mountain low-grade gold-silver deposit. Several other areas have potential for a variety of mineral deposits. Altogether the geochemical, geochronologic, mineralogic, and geologic evidence suggests recurring mineralizing episodes of varied character, from Late Cretaceous to late Tertiary time, related to a long-lived hot spot deep in the crust or in the upper mantle. Granite plutons of Late Cretaceous age were minerali

  18. Changes in physical and chemical properties of a dental palladium-silver alloy during metal-porcelain bonding.

    PubMed

    Payan, J; Moya, G E; Meyer, J M; Moya, F

    1986-07-01

    The hardening ability of a dental palladium-silver (Pd-Ag-Sn-In) bonding alloy has been investigated, and the distribution of the elements along the metal-ceramic interface have been studied by microprobe analysis. The alloy was found to be highly heterogeneous in its 'as-cast' condition, but homogenized alloy was obtained after heating the alloy at 1000 degrees C for 2 h. Hardening occurred after annealing at 650 degrees C for 1 h. A longer thermal treatment caused the hardness to decrease (over-ageing). The change in hardness could be attributed to an internal oxidation phenomenon. The additional elements tin and indium segregated towards the ceramic-metal interface, with a diffusion of indium only into the porcelain. Diffusion of silver in the ceramics, supposed to be the cause of the 'greening' of dental porcelains baked on silver-rich alloys, has not been detected by the microprobe across the interface. PMID:3531444

  19. Concentrations of mercury and other metals in black bass (Micropterus spp.) from Whiskeytown Lake, Shasta County, California, 2005

    USGS Publications Warehouse

    May, Jason T.; Hothem, Roger L.; Bauer, Marissa L.; Brown, Larry R.

    2012-01-01

    This report presents the results of a reconnaissance study conducted by the U.S. Geological Survey (USGS) to determine mercury (Hg) and other selected metal concentrations in Black bass (Micropterus spp.) from Whiskeytown Lake, Shasta County, California. Total mercury concentrations were determined by cold-vapor atomic absorption spectroscopy (CVAAS) in fillets and whole bodies of each sampled fish. Selected metals scans were performed on whole bodies (less the fillets) by inductively coupled plasma–mass spectroscopy (ICP-MS) and inductively coupled plasma–optical emission spectroscopy (ICP-OES). Mercury concentrations in fillet samples ranged from 0.06 to 0.52 micrograms per gram (μg/g) wet weight (ww). Total mercury (HgT) in the same fish whole-body samples ranged from 0.04 to 0.37 (μg/g, ww). Mercury concentrations in 17 percent of "legal catch size" (≥305 millimeters in length) were above the U.S. Environmental Protection Agency water-quality criterion for the protection of human health of 0.30 μg/g (ww). These data will serve as a baseline for future monitoring efforts within Whiskeytown Lake.

  20. Ink jet printable silver metallization with zinc oxide for front side metallization for micro crystalline silicon solar cells

    NASA Astrophysics Data System (ADS)

    Jurk, Robert; Fritsch, Marco; Eberstein, Markus; Schilm, Jochen; Uhlig, Florian; Waltinger, Andreas; Michaelis, Alexander

    2015-12-01

    Ink jet printable water based inks are prepared by a new silver nanoparticle synthesis and the addition of nanoscaled ZnO particles. For the formation of front side contacts the inks are ink jet printed on the front side of micro crystalline silicon solar cells, and contact the cell directly during the firing step by etching through the wafers’ anti-reflection coating (ARC). In terms of Ag dissolution and precipitation the mechanism of contact formation can be compared to commercial glass containing thick film pastes. This avoids additional processing steps, like laser ablation, which are usually necessary to open the ARC prior to ink jet printing. As a consequence process costs can be reduced. In order to optimize the ARC etching and contact formation during firing, zinc oxide nanoparticles are investigated as an ink additive. By utilization of in situ contact resistivity measurements the mechanism of contacting was explored. Our results show that silver inks containing ZnO particles realize a specific contact resistance below 10 mΩṡcm2. By using a multi-pass ink jet printing and plating process a front side metallization of commercial 6  ×  6 inch2 standard micro crystalline silicone solar cells with emitter resistance of 60 Ω/◽ was achieved and showed an efficiency of 15.7%.

  1. Detection of micronuclei in peripheral erythrocytes of Cyprinus carpio exposed to metallic mercury.

    PubMed

    Nepomuceno, J C; Ferrari, I; Spanó, M A; Centeno, A J

    1997-01-01

    Cyprinus carpio fish (carp), exposed to elemental or metallic mercury (Hg0) at concentrations of 2.0, 20.0, and 200.0 mg per liter of water, were kept in concrete tanks for 159 days. Ten fish were used for each concentration level. Thirteen samples of peripheral blood were collected from each animal through gill puncture, 12 during the first 90 days of the experiment, and the last one at the end of the experiment. The micronucleus test (MNT) was designed to study dose and time yield effects of mercury after indirect exposure in vivo. The results indicated that for a concentration of 2.0 mg Hg0/l, there was no significant increase in frequency of micronuclei (MN), but at higher concentrations (20.0 and 200.0 mg Hg0/l) there was a significant increase in MN frequencies. This effect was higher after 31 days of exposure, followed by slight stabilization and gradual decrease. PMID:9366907

  2. Influence of silver nanoparticles on heavy metals of pore water in contaminated river sediments.

    PubMed

    Tao, Wei; Chen, Guiqiu; Zeng, Guangming; Yan, Ming; Chen, Anwei; Guo, Zhi; Huang, Zhenzhen; He, Kai; Hu, Liang; Wang, Lichao

    2016-11-01

    Despite the increasing knowledge on the discharge of silver nanoparticles (AgNPs) into the environment and their potential toxicity to microorganisms, the interaction of AgNPs with heavy metals remains poorly understood. This study focused on the effect of AgNPs on heavy metal concentration and form in sediment contaminated with heavy metals from the Xiangjiang River. The results showed that the concentration of Cu, Zn, Pb and Cd decreased and then increased with a change in form. The changes in form and concentrations of heavy metals in pore water suggested that Cu and Zn were more likely to be affected compared to Pb and Cd. The concentrations of Hg in sediment pore water in three AgNPs-dosed containers, increased greatly until they reached their peaks at 4.468 ± 0.133, 4.589 ± 0.235, and 5.083 ± 0.084 μg L(-1) in Bare AgNPs, Citrate AgNPs and Tween 80 AgNPs, respectively. The measurements of Hg concentrations in the sediment pore water, combined with SEM and EDX analysis, demonstrated that added AgNPs stabilized in pore water and formed an amalgam with Hg(0), which can affect Hg transportation over long distance. PMID:27494311

  3. In vitro cardiotoxicity screening of silver and metal oxide nanoparticles using human induced pluripotent stem cell-derived cardiomyocytes

    EPA Science Inventory

    Exposure risk to silver and metal oxide nanoparticles (NPs) continues to increase due to their widespread use in products and applications. In vivo studies have shown Ag, TiO2 and CeO2 NPs translocate to the heart following various routes of exposure. Thus, it is critical to asse...

  4. Polydopamine as an intermediate layer for silver and hydroxyapatite immobilisation on metallic biomaterials surface.

    PubMed

    Saidin, Syafiqah; Chevallier, Pascale; Abdul Kadir, Mohammed Rafiq; Hermawan, Hendra; Mantovani, Diego

    2013-12-01

    Hydroxyapatite (HA) coated implant is more susceptible to bacterial infection as the micro-structure surface which is beneficial for osseointegration, could also become a reservoir for bacterial colonisation. The aim of this study was to introduce the antibacterial effect of silver (Ag) to the biomineralised HA by utilising a polydopamine film as an intermediate layer for Ag and HA immobilisation. Sufficient catechol groups in polydopamine were required to bind chemically stainless steel 316 L, Ag and HA elements. Different amounts of Ag nanoparticles were metallised on the polydopamine grafted stainless steel by varying the immersion time in silver nitrate solution from 12 to 24 h. Another polydopamine layer was then formed on the metallised film, followed by surface biomineralisation in 1.5 Simulated Body Fluid (SBF) solution for 3 days. Several characterisation techniques including X-Ray Photoelectron Spectroscopy, Atomic Force Microscopy, Scanning Electron Microscopy and Contact Angle showed that Ag nanoparticles and HA agglomerations were successfully immobilised on the polydopamine film through an element reduction process. The Ag metallisation at 24 h has killed the viable bacteria with 97.88% of bactericidal ratio. The Ag was ionised up to 7 days which is crucial to prevent bacterial infection during the first stage of implant restoration. The aged functionalised films were considered stable due to less alteration of its chemical composition, surface roughness and wettability properties. The ability of the functionalised film to coat complex and micro scale metal make it suitable for dental and orthopaedic implants application. PMID:24094179

  5. DNA-Metalization: Synthesis and Properties of Novel Silver-Containing DNA Molecules (Adv. Mater. 24/2016).

    PubMed

    Eidelshtein, Gennady; Fardian-Melamed, Natalie; Gutkin, Vitaly; Basmanov, Dmitry; Klinov, Dmitry; Rotem, Dvir; Levi-Kalisman, Yael; Porath, Danny; Kotlyar, Alexander

    2016-06-01

    D. Porath, A. Kotlyar, and co-workers transform DNA to a conducting material by metalization through coating or chemical modifications, as described on page 4839. Specific and reversible metalization of poly(dG)-poly(dC) DNA by migration of atoms from silver nanoparticles to the DNA is demonstrated. As the transformation occurs gradually, novel, truly hybrid molecular structures are obtained, paving the way to their usage as nanowires in programmable molecular electronic devices and circuits. PMID:27311096

  6. Rapid, selective, and ultrasensitive fluorimetric analysis of mercury and copper levels in blood using bimetallic gold-silver nanoclusters with "silver effect"-enhanced red fluorescence.

    PubMed

    Zhang, Ning; Si, Yanmei; Sun, Zongzhao; Chen, Lijun; Li, Rui; Qiao, Yuchun; Wang, Hua

    2014-12-01

    Bimetallic alloying gold-silver nanoclusters (Au-AgNCs) have been synthesized by a one-pot biomineralization synthesis route at a vital molar ratio of Au/Ag precursors in the protein matrix. Unexpectedly, the prepared Au-AgNCs could exhibit dramatically enhanced red fluorescence, which is about 6.5-fold and 4.7-fold higher than that of common AuNCs and core-shell Au@AgNCs, respectively. A rapid, selective, and ultrasensitive fluorimetric method has thereby been developed using Au-AgNCs as fluorescent probes toward the separate detections of Hg(2+) and Cu(2+) ions in blood. The interactions of Au-AgNCs with Hg(2+) and Cu(2+) ions were systematically characterized by microscopy imaging, UV-vis, and fluorescence measurements. It is demonstrated that the "silver effect" gives the Au-AgNCs probes not only greatly enhanced red fluorescence but also the strong capacity to specifically sense Cu(2+) ions in addition to improved response to Hg(2+) ions. Moreover, aided by a Cu(2+) chelating agent, exclusive detection of Hg(2+) ions could also be expected with the coexistence of a high level of Cu(2+) ions, as well as reversible Cu(2+) analysis by restoring the fluorescence of Au-AgNCs. Additionally, Au-AgNCs with strong red fluorescence could facilitate fluorimetric analysis with minimal interference from blood backgrounds. Such an Au-AgNCs-based fluorimetric method can allow for the selective analysis of Hg(2+) and Cu(2+) ions down to 0.30 nM and 0.60 nM in blood, respectively, promising a novel detection method to be applied in the clinical laboratory. PMID:25350497

  7. Adsorption of silver nanoparticles from aqueous solution on copper-based metal organic frameworks (HKUST-1).

    PubMed

    Conde-González, J E; Peña-Méndez, E M; Rybáková, S; Pasán, J; Ruiz-Pérez, C; Havel, J

    2016-05-01

    Silver nanoparticles (AgNP) are emerging pollutants. The use of novel materials such as Cu-(benzene 1,3,5-tricarboxylate, BTC) Metal-Organic Framework (MOFs), for AgNP adsorption and their removal from aqueous solutions has been studied. The effect of different parameters was followed and isotherm model was suggested. MOFs adsorbed fast and efficiently AgNP in the range C0 < 10 mg L(-1), being Freundlich isotherm (R = 0.993) these data fitted to. Among studied parameters a remarkable effect of chloride on sorption was found, thus their possible interactions were considered. The high adsorption efficiency of AgNP was achieved and it was found to be very fast. The feasibility of adsorption on Cu-(BTC) was proved in spiked waters. The results showed the potential interest of new material as adsorbent for removing AgNP from environment. PMID:26879292

  8. Silver Nanowire Top Electrodes in Flexible Perovskite Solar Cells using Titanium Metal as Substrate.

    PubMed

    Lee, Minoh; Ko, Yohan; Min, Byoung Koun; Jun, Yongseok

    2016-01-01

    Flexible perovskite solar cells (FPSCs) have various applications such as wearable electronic textiles and portable devices. In this work, we demonstrate FPSCs on a titanium metal substrate employing solution-processed silver nanowires (Ag NWs) as the top electrode. The Ag NW electrodes were deposited on top of the spiro-MeOTAD hole transport layer by a carefully controlled spray-coating method at moderate temperatures. The power conversion efficiency (PCE) reached 7.45 % under AM 1.5 100 mW cm(-2) illumination. Moreover, the efficiency for titanium-based FPSCs decreased only slightly (by 2.6 % of the initial value) after the devices were bent 100 times. With this and other advances, fully solution-based indium-free flexible photovoltaics, advantageous in terms of price and processing, have the potential to be scaled into commercial production. PMID:26612081

  9. THE DETERMINATION OF MERCURY AND MULTIPLE METALS IN DIETARY MATRICES USING DIRECT INJECTION NEBULIZATION INDUCTIVELY COUPLED PLASMA MASS SPECTROMETRY (DIN-ICP/MS)

    EPA Science Inventory

    Mercury (Hg) is a Persistent Bioaccumulative Toxin. Currently, low-level mercury (Hg) and low-level multiple-metals analyses require separate methods. Due to the high costs of performing both types of analyses, research planners often have to choose one or the other. For examp...

  10. Mercury and mercury compounds toxicology. (Latest citations from the Life Sciences Collection data base). Published Search

    SciTech Connect

    Not Available

    1992-10-01

    The bibliography contains citations concerning the toxic effects of mercury and mercury compounds on biological systems. Mercury metal, mercury vapors, organic mercury compounds, mercury halides, and other inorganic mercury compounds are discussed. Citations include acute, chronic, environmental, metabolic, and pathological effects; and clinical biochemistry of mercury exposure. Heavy metal pollution and bioaccumulation are referenced in related bibliographies. (Contains 250 citations and includes a subject term index and title list.)

  11. Mercury and mercury compounds toxicology. (Latest citations from the Life Sciences Collection database). Published Search

    SciTech Connect

    Not Available

    1994-04-01

    The bibliography contains citations concerning the toxic effects of mercury and mercury compounds on biological systems. Mercury metal, mercury vapors, organic mercury compounds, mercury halides, and other inorganic mercury compounds are discussed. Citations include acute, chronic, environmental, metabolic, and pathological effects; and clinical biochemistry of mercury exposure. Heavy metal pollution and bioaccumulation are referenced in related bibliographies. (Contains 250 citations and includes a subject term index and title list.)

  12. Organic and inorganic mercurials have distinct effects on cellular thiols, metal homeostasis, and Fe-binding proteins in Escherichia coli.

    PubMed

    LaVoie, Stephen P; Mapolelo, Daphne T; Cowart, Darin M; Polacco, Benjamin J; Johnson, Michael K; Scott, Robert A; Miller, Susan M; Summers, Anne O

    2015-12-01

    The protean chemical properties of the toxic metal mercury (Hg) have made it attractive in diverse applications since antiquity. However, growing public concern has led to an international agreement to decrease its impact on health and the environment. During a recent proteomics study of acute Hg exposure in E. coli, we also examined the effects of inorganic and organic Hg compounds on thiol and metal homeostases. On brief exposure, lower concentrations of divalent inorganic mercury Hg(II) blocked bulk cellular thiols and protein-associated thiols more completely than higher concentrations of monovalent organomercurials, phenylmercuric acetate (PMA) and merthiolate (MT). Cells bound Hg(II) and PMA in excess of their available thiol ligands; X-ray absorption spectroscopy indicated nitrogens as likely additional ligands. The mercurials released protein-bound iron (Fe) more effectively than common organic oxidants and all disturbed the Na(+)/K(+) electrolyte balance, but none provoked efflux of six essential transition metals including Fe. PMA and MT made stable cysteine monothiol adducts in many Fe-binding proteins, but stable Hg(II) adducts were only seen in CysXxx(n)Cys peptides. We conclude that on acute exposure: (a) the distinct effects of mercurials on thiol and Fe homeostases reflected their different uptake and valences; (b) their similar effects on essential metal and electrolyte homeostases reflected the energy dependence of these processes; and (c) peptide phenylmercury-adducts were more stable or detectable in mass spectrometry than Hg(II)-adducts. These first in vivo observations in a well-defined model organism reveal differences upon acute exposure to inorganic and organic mercurials that may underlie their distinct toxicology. PMID:26498643

  13. In vitro studies on silver implanted pure iron by metal vapor vacuum arc technique.

    PubMed

    Huang, Tao; Cheng, Yan; Zheng, Yufeng

    2016-06-01

    Pure iron has been verified as a promising biodegradable metal for absorbable cardiovascular stent usage. However, the degradation rate of pure iron is too slow. To accelerate the degradation of the surface of pure iron, silver ions were implanted into pure iron by metal vapor vacuum arc (MEVVA) source at an extracted voltage of 40keV. The implanted influence was up to 2×10(17)ions/cm(2). The composition and depth profiles, corrosion behavior and biocompatibility of Ag ion implanted pure iron were investigated. The implantation depths of Ag was around 60nm. The element Ag existed as Ag2O in the outermost layer, then gradually transited to metal atoms in zero valent state with depth increase. The implantation of Ag ions accelerated the corrosion rate of pure iron matrix, and exhibited much more uniform corrosion behavior. For cytotoxicity assessment, the implantation of Ag ions slightly decreased the viability of all kinds of cell lines used in these tests. The hemolysis rate of Ag ion implanted pure iron was lower than 2%, which was acceptable, whereas the platelet adhesion tests indicated the implantation of Ag ions might increase the risk of thrombosis. PMID:26925722

  14. Mercury in various tissues of three mustelid species and other trace metals in liver of European otter from Eastern Finland.

    PubMed

    Lodenius, M; Skarén, U; Hellstedt, P; Tulisalo, E

    2014-01-01

    Mercury concentrations were monitored in European otter (Lutra lutra), European polecat (Mustela putorius) and European pine marten (Martes martes) collected in Eastern Finland during the period 1972-2008. Otters mainly eat fish, which is an important reason to monitor the bioaccumulation of mercury in this predator. In this species, the highest concentrations were found in fur followed by liver and kidney, and the mercury concentrations increased with increasing age and body weight. Males showed in general higher concentrations than females of otters. The food of European polecat consists of small mammals, frogs, birds and insects from both aquatic and terrestrial food chains. The mercury concentrations were lower than in otters without significant differences related to body weight or sex. In European pine martens, the concentrations were rather evenly distributed except for two specimens with high concentrations. Also, concentrations of some other metals (Al, Cd, Cu, Fe, Mn, Ni, Pb and Zn) were analysed from liver samples of otter. Possible adverse effects of mercury on the Finnish populations of these mustelids are discussed. PMID:23974535

  15. High temperature silver-palladium-copper oxide air braze filler metal

    NASA Astrophysics Data System (ADS)

    Darsell, Jens Tommy

    The Ag-CuO system is currently being investigated as the basis for an air braze filler metal alloy to be used in SOFC components. The system is of interest because unlike most braze alloys, it is capable of wetting a variety of ceramic materials while being applied in an air. This thesis work examined modification of Ag-CuO filler metal system by alloying with palladium to increase the use temperature of the resulting air braze alloy. Thermal analysis was performed to track changes in the solidus and liquidus temperatures for these alloys and determine equilibrium phase present as a function of temperature and composition. Sessile drop experiments were performed to investigate the effect of palladium addition on braze wetability. The influence of copper-oxide and palladium contents on brazed joint strength was characterized by a combination of four-point bend testing and fractography. From combined thermal analysis and quenched data it was found that both the liquidus and solidus increase with increasing palladium content, and the silver-rich miscibility gap boundary could be shifted by the addition of palladium. This was employed as a tool to study the effects of two-liquid phase formation on wetting behavior. In addition, a mass loss likely attributable to silver volatilization is observed in the Pd-modified filler metals when heated over ˜1100°C. As volatilization should be avoided, the ternary alloys should be limited to 15mol% Pd. It was found by sessile drop wetting experiments that there is a definitive change in wetting behavior that corresponds directly to the miscibility gap boundary for the Pd-Ag-CuO system. The first order transition tracks with changes in the miscibility gap boundary that can be induced by increasing palladium content. This is the first experimental evidence of critical point wetting behavior reported for a metal-oxide system and further confirms that critical point wetting theory is universal. Four-point bend testing and

  16. Plasmonic enhancement in upconversion emission of La2O3:Er3+/Yb3+ phosphor via introducing silver metal nanoparticles

    NASA Astrophysics Data System (ADS)

    Tiwari, S. P.; Kumar, K.; Rai, V. K.

    2015-11-01

    In the present work, authors have synthesized silver (Ag) nanoparticle (NP) embedded La2O3:Er3+/Yb3+ powder phosphor. The synthesis method has resulted in silver oxide-lanthanum oxide composite material. Through subsequent heat treatment of sample in pellet form, the silver metal nanoparticles were formed. The presence of plasmonic Ag NPs in the matrix is confirmed by various techniques. Large enhancement in downconversion as well as upconversion emission intensity of Er3+ ions at various concentrations of Ag NPs is obtained. Large enhancement in the upconversion emission intensity is correlated to the reduction in decay time of 4S3/2 level in the presence of Ag NPs, and possible reasons for intensity enhancement are discussed. The application of phosphor in fingermark detection is demonstrated.

  17. The direct determination of trace metals in gold and silver materials by laser ablation inductively coupled plasma mass spectrometry without matrix matched standards

    NASA Astrophysics Data System (ADS)

    Kogan, Valentina V.; Hinds, Michael W.; Ramendik, Gregory I.

    1994-04-01

    Typically, accurate trace element determination in solid samples by laser ablation ICP-MS requires calibration with matrix matched standards. Trace metal analysis was performed in high purity gold, high purity silver and 14 karat gold-silver alloys. A Nd : YAG laser was used to evaporate solid samples of precious metals into an inductively coupled plasma mass spectrometer. Analytical data and a study of the crater sizes indicated that approximately the same amount of material for both gold and silver samples was vaporized by a Nd : YAG laser operated in a Q-switched mode with the following parameters: 210 mJ laser energy; 8 Hz repetition rate; and focused 7 mm below the sample surface. High purity gold and silver, and a 14 karat gold-silver alloy were analyzed for trace metals common to gold and silver reference materials. In general, the determination of Fe, Ni, Cu, Zn, Pd, Pt, Pb, and Bi did not strongly depend on whether gold or silver reference materials were used for calibration. This permits these trace metals to be determined directly with only one set of reference materials, by laser ablation ICP-MS, in a wide variety of gold-silver alloys.

  18. WATER QUALITY, MERCURY, AND HEAVY METAL DEPOSITION STUDIES IN BIOLOGICAL SPECIMENS AND SEDIMENTS FOR ECOLOGICAL BASELINE DATA IN THE ISLAND PARK WATERWAYS SYSTEM, 1973

    EPA Science Inventory

    The water quality, mercury, and heavy metal deposition in biological specimens from the Island Park waterways (17040202) were measured to establish ecological baseline data. Neutron activation analysis was used to identify quantitatively and qualitatively approximately 20 differ...

  19. Effect of Mercury-Noble Metal Interactions on SRAT Processing of SB3 Simulants (U)

    SciTech Connect

    Koopman, D. C.; Baich, M. A.

    2004-12-31

    Controlling hydrogen generation below the Defense Waste Processing Facility (DWPF) safety basis constrains the range of allowable acid additions in the DWPF Chemical Processing Cell. This range is evaluated in simulant tests at the Savannah River National Laboratory (SRNL). A minimum range of allowable acid additions is needed to provide operational flexibility and to handle typical uncertainties in process and analytical measurements used to set acid additions during processing. The range of allowable acid additions is a function of the composition of the feed to DWPF. Feed changes that lead to a smaller range of allowable acid additions have the potential to impact decisions related to wash endpoint control of DWPF feed composition and to the introduction of secondary waste streams into DWPF. A limited program was initiated in SRNL in 2001 to study the issue of hydrogen generation. The program was reinitiated at the end of fiscal year 2004. The primary motivation for the study is that a real potential exists to reduce the conservatism in the range of allowable acid additions in DWPF. Increasing the allowable range of acid additions can allow decisions on the sludge wash endpoint or the introduction of secondary waste streams to DWPF to be based on other constraints such as glass properties, organic carbon in the melter off-gas, etc. The initial phase of the study consisted of a review of site reports and off-site literature related to catalytic hydrogen generation from formic acid and/or formate salts by noble metals. Many things are already known about hydrogen generation during waste processing. This phase also included the development of an experimental program to improve the understanding of hydrogen generation. This phase is being documented in WSRC-TR-2002-00034. A number of areas were identified where an improved understanding would be beneficial. A phased approach was developed for new experimental studies related to hydrogen generation. The first phase

  20. Acute toxicity modeling of rainbow trout and silver sea bream exposed to waterborne metals.

    PubMed

    Liao, C M; Lin, M C

    2001-01-01

    Of three proposed acute toxicity models, the uptake-depuration (UD) model, the time-integrated concentration (TIC) model, and the concentration-time (CT) model are derived and verified with acute toxicity data to estimate the internal residues of waterborne metals in fish as a function of a few constants and variables. The main factors are the exposure time, the external exposure concentration, the bioconcentration factor (BCF), and the depuration rate constant (k2). The UD model is based on the concept of residue levels at the cell membrane well correlating with the whole-body concentrations, whereas the TIC and the CT models are based on the idea of irreversible inhibition of the enzyme acetylcholinesterase (AChE) governing the metal acute toxicity in that metals in the entire fish or in the aqueous phase can be described by the critical area under the time-concentration curve that is associated with a critical TIC of toxicant in the target tissue. A highly significant correlation (r2 > 0.9) was found between predictions and LC50(t) data for both the TIC and the CT models, indicating successfully describe 4- to 18-d LC50(t) data of arsenic (As), cobalt (Co), copper (Cu), and Co/Cu mixture in rainbow trout (Oncorhyuchus mykiss) and of Cu in fingerlings and subadults of silver sea bream (Sparus sarba). The time-dependent lethal internal concentration at the site of action that causes 50% mortality is also predicted for a given compound and species. It concludes that the TIC and the CT models can be applied to regulate the acute toxicity and to estimate incipient LC50 values and internal residues of waterborne metals in fish. PMID:11501285

  1. Metal mercury poisoning in two boys initially treated for brucellosis in Mashhad, Iran.

    PubMed

    Sasan, M S; Hadavi, N; Afshari, R; Mousavi, S R; Alizadeh, A; Balali-Mood, Mahdi

    2012-02-01

    Elemental mercury (Hg) is the only metal which evaporates in room temperature and its inhalation may cause toxicity. Hg poisoning may occur by mishandling the metal, particularly in children who play with it. Wide-spectrum of the clinical presentations of chronic Hg poisoning may cause misdiagnosis, particularly when history of exposure is unknown. We report two cases of accidental Hg poisoning, which initially had been diagnosed and treated for brucellosis. The patients were two brothers (7 and 14 years old) who presented with pain in their lower extremities, sweating, salivation, weight loss, anorexia and mood changes on admission. Meticulous history taking revealed that they had played with a ball of Hg since 3 months before admission. The level of urinary Hg was 125.9 and 54.2 9 g/L in the younger and older brother, respectively (normal ≤25 g/L). The patients were successfully treated by dimercaprol and discharged in good condition 24 days after admission. These cases are being reported to emphasize the importance of acrodynia as a differential diagnosis for brucellosis in endemic areas. PMID:21803782

  2. Label-free SERS study of galvanic replacement reaction on silver nanorod surface and its application to detect trace mercury ion

    PubMed Central

    Wang, Yaohui; Wen, Guiqing; Ye, Lingling; Liang, Aihui; Jiang, Zhiliang

    2016-01-01

    It is significant to explore a rapid and highly sensitive galvanic replacement reaction (GRR) surface enhanced Raman scattering (SERS) method for detection of trace mercury ions. This article was reported a new GRR SERS analytical platform for detecting Hg(II) with label-free molecular probe Victoria blue B (VBB). In HAc-NaCl-silver nanorod (AgNR) substrate, the molecular probe VBB exhibited a strong SERS peak at 1609 cm−1. Upon addition of Hg(II), the GRR occurred between the AgNR and Hg(II), and formed a weak SERS activity of Hg2Cl2 that deposited on the AgNR surfaces to decrease the SERS intensity at 1609 cm−1. The decreased SERS intensity was linear to Hg(II) concentration in the range of 1.25–125 nmol/L, with a detection limit of 0.2 nmol/L. The GRR was studied by SERS, transmission electron microscopy and other techniques, and the GRR mechanism was discussed. PMID:26792071

  3. Investigation of protein FTT1103 electroactivity using carbon and mercury electrodes. Surface-inhibition approach for disulfide oxidoreductases using silver amalgam powder.

    PubMed

    Večerková, Renata; Hernychová, Lenka; Dobeš, Petr; Vrba, Jiří; Josypčuk, Bohdan; Bartošík, Martin; Vacek, Jan

    2014-06-01

    Recently, it was shown that electrochemical methods can be used for analysis of poorly water-soluble proteins and for study of their structural changes and intermolecular (protein-ligand) interactions. In this study, we focused on complex electrochemical investigation of recombinant protein FTT1103, a disulfide oxidoreductase with structural similarity to well described DsbA proteins. This thioredoxin-like periplasmic lipoprotein plays an important role in virulence of bacteria Francisella tularensis. For electrochemical analyses, adsorptive transfer (ex situ) square-wave voltammetry with pyrolytic graphite electrode, and alternating-current voltammetry and constant-current chronopotentiometric stripping analysis with mercury electrodes, including silver solid amalgam electrode (AgSAE) were used. AgSAE was used in poorly water-soluble protein analysis for the first time. In addition to basic redox, electrocatalytic and adsorption/desorption characterization of FTT1103, electrochemical methods were also used for sensitive determination of the protein at nanomolar level and study of its interaction with surface of AgSA microparticles. Proposed electrochemical protocol and AgSA surface-inhibition approach presented here could be used in future for biochemical studies focused on proteins associated with membranes as well as on those with disulfide oxidoreductase activity. PMID:24856508

  4. Mercury and other metals in eggs and feathers of glaucous-winged gulls (Larus glaucescens) in the Aleutians

    PubMed Central

    Gochfeld, Michael; Jeitner, Christian; Burke, Sean; Volz, Conrad D.; Snigaroff, Ronald; Snigaroff, Daniel; Shukla, Tara; Shukla, Sheila

    2014-01-01

    Levels of mercury and other contaminants should be lower in birds nesting on isolated oceanic islands and at high latitudes without any local or regional sources of contamination, compared to more urban and industrialized temperate regions. We examined concentrations of arsenic, cadmium, chromium, lead, manganese, mercury and selenium in the eggs, and the feathers of fledgling and adult glaucous-winged gulls (Larus glaucescens) nesting in breeding colonies on Adak, Amchitka, and Kiska Islands in the Aleutian Chain of Alaska in the Bering Sea/North Pacific. We tested the following null hypotheses: 1) There were no differences in metal levels among eggs and feathers of adult and fledgling glaucous-winged gulls, 2) There were no differences in metal levels among gulls nesting near the three underground nuclear test sites (Long Shot 1965, Milrow 1969, Cannikin 1971) on Amchitka, 3) There were no differences in metal levels among the three islands, and 4) There were no gender-related differences in metal levels. All four null hypotheses were rejected at the 0.05 level, although there were few differences among the three test sites on Amchitka. Eggs had the lowest levels of cadmium, lead, and mercury, and the feathers of adults had the lowest levels of selenium. Comparing only adults and fledglings, adults had higher levels of cadmium, chromium, lead and mercury, and fledglings had higher levels of arsenic, manganese and selenium. There were few consistent interisland differences, although levels were generally lower for eggs and feathers from gulls on Amchitka compared to the other islands. Arsenic was higher in both adult feathers and eggs from Amchitka compared to Adak, and chromium and lead were higher in adult feathers and eggs from Adak compared to Amchitka. Mercury and arsenic, and chromium and manganese levels were significantly correlated in the feathers of both adult and fledgling gulls. The feathers of males had significantly higher levels of chromium and

  5. Heavy metal and radionuclide concentrations in fly ash material

    SciTech Connect

    Booker, J.D.; Phagan, C.J.; Gray, R.H.

    1995-12-31

    A study was completed to characterize the concentrations of heavy metals and radionuclides and their mobility in two fly ash covered parking lots at the US Department of Energy`s Pantex Plant. Six composite samples collected from the parking areas were analyzed by an offsite contract laboratory for arsenic, barium, cadmium, chromium, lead, mercury, selenium, silver, uranium 234, and uranium 238. All metal and radionuclide concentrations except mercury and silver exceeded the applicable comparison standards for typical Pantex Plant soil; however, concentrations of mercury and silver were significantly below the Texas Risk Reduction Standards. In view of these results, it was strongly recommended that fly ash not be used for future projects at the Pantex Plant unless specialized engineering controls are used.

  6. One-pot green synthesis of high quantum yield oxygen-doped, nitrogen-rich, photoluminescent polymer carbon nanoribbons as an effective fluorescent sensing platform for sensitive and selective detection of silver(I) and mercury(II) ions.

    PubMed

    Wang, Zhong-Xia; Ding, Shou-Nian

    2014-08-01

    This work reports on a facile, economical, and green preparative strategy toward water-soluble, fluorescent oxygen-doped, nitrogen-rich, photoluminescent polymer carbon nanoribbons (ONPCRs) with a quantum yield of approximately 25.61% by the hydrothermal process using uric acid as a carbon-nitrogen source for the first time. The as-prepared fluorescent ONPCRs showed paddy leaf-like structure with 80-160 nm length and highly efficient fluorescent quenching ability in the presence of mercury(II) (Hg(2+)) or silver (Ag(+)) ions due to the formed nonfluorescent metal complexes via robust Hg(2+)-O or Ag(+)-N interaction with the O and N of fluorescent ONPCRs, which allowed the analysis of Hg(2+) and Ag(+) ions in a very simple method. By employing this sensor, excellent linear relationships existed between the quenching degree of the ONPCRs and the concentrations of Hg(2+) and Ag(+) ions in the range of 2.0 nM to 60 μM and 5.0 nM to 80 μM, respectively. By using ethylenediaminetetraacetate and ammonia as the masking agent of Hg(2+) and Ag(+) ions, respectively, Hg(2+) or Ag(+) ions were exclusively detected in coexistence with Ag(+) or Hg(2+) ions with high sensitivity, and the detection limits as low as 0.68 and 1.73 nM (3σ) were achieved, respectively, which also provided a reusable detection method for Hg(2+) and Ag(+) ions. Therefore, the easily synthesized fluorescent ONPCRs may have great potential applications in the detection of Hg(2+) and Ag(+) ions for biological assay and environmental protection. PMID:24979236

  7. Correlation of photobleaching, oxidation and metal induced fluorescence quenching of DNA-templated silver nanoclusters

    NASA Astrophysics Data System (ADS)

    Morishita, Kiyoshi; Maclean, James L.; Liu, Biwu; Jiang, Hui; Liu, Juewen

    2013-03-01

    Few-atom noble metal nanoclusters have attracted a lot of interest due to their potential applications in biosensor development, imaging and catalysis. DNA-templated silver nanoclusters (AgNCs) are of particular interest as different emission colors can be obtained by changing the DNA sequence. A popular analytical application is fluorescence quenching by Hg2+, where d10-d10 metallophilic interaction has often been proposed for associating Hg2+ with nanoclusters. However, it cannot explain the lack of response to other d10 ions such as Zn2+ and Cd2+. In our effort to elucidate the quenching mechanism, we studied a total of eight AgNCs prepared by different hairpin DNA sequences; they showed different sensitivity to Hg2+, and DNA with a larger cytosine loop size produced more sensitive AgNCs. In all the cases, samples strongly quenched by Hg2+ were also more easily photobleached. Light of shorter wavelengths bleached AgNCs more potently, and photobleached samples can be recovered by NaBH4. Strong fluorescence quenching was also observed with high redox potential metal ions such as Ag+, Au3+, Cu2+ and Hg2+, but not with low redox potential ions. Such metal induced quenching cannot be recovered by NaBH4. Electronic absorption and mass spectrometry studies offered further insights into the oxidation reaction. Our results correlate many important experimental observations and will fuel the further growth of this field.Few-atom noble metal nanoclusters have attracted a lot of interest due to their potential applications in biosensor development, imaging and catalysis. DNA-templated silver nanoclusters (AgNCs) are of particular interest as different emission colors can be obtained by changing the DNA sequence. A popular analytical application is fluorescence quenching by Hg2+, where d10-d10 metallophilic interaction has often been proposed for associating Hg2+ with nanoclusters. However, it cannot explain the lack of response to other d10 ions such as Zn2+ and Cd2+. In

  8. Method for the removal and recovery of mercury

    DOEpatents

    Easterly, C.E.; Vass, A.A.; Tyndall, R.L.

    1997-01-28

    The present invention is an enhanced method for the removal and recovery of mercury from mercury-contaminated matrices. The method involves contacting a mercury-contaminated matrix with an aqueous dispersant solution derived from specific intra-amoebic isolates to release the mercury from the mercury-contaminated matrix and emulsify the mercury; then, contacting the matrix with an amalgamating metal from a metal source to amalgamate the mercury to the amalgamating metal; removing the metallic source from the mercury-contaminated matrix; and heating the metallic source to vaporize the mercury in a closed system to capture the mercury vapors.

  9. Method for the removal and recovery of mercury

    DOEpatents

    Easterly, Clay E.; Vass, Arpad A.; Tyndall, Richard L.

    1997-01-01

    The present invention is an enhanced method for the removal and recovery of mercury from mercury-contaminated matrices. The method involves contacting a mercury-contaminated matrix with an aqueous dispersant solution derived from specific intra-amoebic isolates to release the mercury from the mercury-contaminated matrix and emulsify the mercury; then, contacting the matrix with an amalgamating metal from a metal source to amalgamate the mercury to the amalgamating metal; removing the metallic source from the mercury-contaminated matrix; and heating the metallic source to vaporize the mercury in a closed system to capture the mercury vapors.

  10. [Evaluation of cervical gaps in complete metal crowns cast in alternative silver-tin alloys. Relationship to investing techniques].

    PubMed

    Vecchio, G M; Pretti, E; Vaz, R R; Zaniquelli, O

    1990-01-01

    The purpose of this study was to evaluate cervical mistifing of casting full metal crowns according to investment techniques using commercial available alloys made from silver stannum. Fifteen metal full crowns were obtained through stainless steel die with full crowns preparation, included into three groups as follows: conventional technique, vacuum technique and pressure technique. Readings of cervical disagreement were made through a comparing microscope increased 45 x and each crown was measured in 4 different regions (vestibular, lingual mesial and distal). This way it was verified which of the techniques proposed would balance the casting shrinkage for the silver-stannum alloy used. From the results obtained we conclude that the best cercical adaptation was the one got through pressure technique. PMID:2135769

  11. Distribution of Mercury and Other Trace Metals in the Wabash River, Indiana

    NASA Astrophysics Data System (ADS)

    Neumann, K.; Bonzongo, J.

    2005-12-01

    There is very little information on mercury (Hg) and other trace metals (e.g., Co, Ni, Cu) in streams of central Indiana. Published research has focused mainly on the industrialized northern part of the State, close to Chicago, and on the Ohio River valley at the southern end of the State. For rivers draining the central part of Indiana, including the Wabash River, numerous Hg-based fish advisories are posted; yet, very little to no data on Hg and trace metals in water or sediments exists. We present some of the first Hg and trace metal data for the Wabash River in central Indiana. Water and surface sediment samples were collected in the summers of 2004 and 2005 from the river section that extends from upstream of Lafayette to Terre Haute. In contrast to the Wabash River upstream reaches, this section of the river has no water inputs from tributaries that drain reservoirs, and the above two cities as well as a power plant located upstream of Terre Haute are potential sources for Hg and trace metals to the river. Total-Hg concentrations determined on filtered samples ranged from 0.57 to 1.7ng/L in samples collected in August 2004, with very little change in concentrations a year after (range: 0.61 to 0.83ng/L). Total Hg levels in non-filtered samples ranged from ~1.6 to 5.0ng/L and from 3.31 to 4.17ng/L in August 2004 and 2005, respectively. These values compare to those reported for rivers and streams in neighboring states. Dissolved trace metal concentrations are generally low (e.g., Co, Ni, Cu less than 2μg/L) and show only small increases as the Wabash River passes through Lafayette. We will examine the relationships between aqueous Hg, sedimentary Hg (0.93-16.8μg/g) and Hg in biological tissues in comparison with trends/levels reported for other US rivers with similar land use types within watersheds.

  12. Synthesis of a nano-silver metal ink for use in thick conductive film fabrication applied on a semiconductor package.

    PubMed

    Yung, Lai Chin; Fei, Cheong Choke; Mandeep, Js; Binti Abdullah, Huda; Wee, Lai Khin

    2014-01-01

    The success of printing technology in the electronics industry primarily depends on the availability of metal printing ink. Various types of commercially available metal ink are widely used in different industries such as the solar cell, radio frequency identification (RFID) and light emitting diode (LED) industries, with limited usage in semiconductor packaging. The use of printed ink in semiconductor IC packaging is limited by several factors such as poor electrical performance and mechanical strength. Poor adhesion of the printed metal track to the epoxy molding compound is another critical factor that has caused a decline in interest in the application of printing technology to the semiconductor industry. In this study, two different groups of adhesion promoters, based on metal and polymer groups, were used to promote adhesion between the printed ink and the epoxy molding substrate. The experimental data show that silver ink with a metal oxide adhesion promoter adheres better than silver ink with a polymer adhesion promoter. This result can be explained by the hydroxyl bonding between the metal oxide promoter and the silane grouping agent on the epoxy substrate, which contributes a greater adhesion strength compared to the polymer adhesion promoter. Hypotheses of the physical and chemical functions of both adhesion promoters are described in detail. PMID:24830317

  13. Synthesis of a Nano-Silver Metal Ink for Use in Thick Conductive Film Fabrication Applied on a Semiconductor Package

    PubMed Central

    Yung, Lai Chin; Fei, Cheong Choke; Mandeep, JS; Binti Abdullah, Huda; Wee, Lai Khin

    2014-01-01

    The success of printing technology in the electronics industry primarily depends on the availability of metal printing ink. Various types of commercially available metal ink are widely used in different industries such as the solar cell, radio frequency identification (RFID) and light emitting diode (LED) industries, with limited usage in semiconductor packaging. The use of printed ink in semiconductor IC packaging is limited by several factors such as poor electrical performance and mechanical strength. Poor adhesion of the printed metal track to the epoxy molding compound is another critical factor that has caused a decline in interest in the application of printing technology to the semiconductor industry. In this study, two different groups of adhesion promoters, based on metal and polymer groups, were used to promote adhesion between the printed ink and the epoxy molding substrate. The experimental data show that silver ink with a metal oxide adhesion promoter adheres better than silver ink with a polymer adhesion promoter. This result can be explained by the hydroxyl bonding between the metal oxide promoter and the silane grouping agent on the epoxy substrate, which contributes a greater adhesion strength compared to the polymer adhesion promoter. Hypotheses of the physical and chemical functions of both adhesion promoters are described in detail. PMID:24830317

  14. One-step synthesis of uniform silver nanoparticles capped by saturated decanoate: direct spray printing ink to form metallic silver films.

    PubMed

    Dong, Teng-Yuan; Chen, Wei-Ting; Wang, Ching-Wen; Chen, Chiao-Pei; Chen, Chen-Ni; Lin, Ming-Cheng; Song, Jenn-Ming; Chen, In-Gann; Kao, Tzu-Hsuan

    2009-08-01

    The one-step synthesis and spectroscopic characterizations of size-controlled silver nanoparticles are described. The transmission electron microscopy (TEM), nuclear magnetic resonance (NMR), Fourier transform infrared spectroscopy (FT-IR), thermal gravimetric-mass analysis (TGA-MS) and X-ray photoelectron spectroscopy (XPS) techniques were used to characterize the decanoate-protected silver nanoparticles. TEM analysis showed that spherical nanoclusters of 7.52 +/- 0.57 nm were produced. Furthermore, the particle sizes are uniform with a narrow size distribution. For all samples, Ag 3d(5/2) and 3d(3/2) components appeared at 368.5 and 374.5 eV, respectively, in the XPS spectrum; these values compare very well with the typical values of carboxylate-protected Ag nanoparticles. A thermal analysis mass spectrometer was used to analyze the desorption behavior of decanoate-protected nanoparticles. From the desorption maximum temperatures of 181 and 263 degrees C, activation energies of 27.2 and 32.2 kcal mol(-1) for the desorption processes in the Ag MPCs were obtained, assuming a first-order reaction and using a pre-exponential factor of 1 x 10(13) s(-1). A specific resistivity of 6.097 microOmega cm for the silver metal film (0.7 microm) on a Si wafer can be produced simply by thermal annealing of an Ag monolayer-protected clusters film under an atmosphere of 90% N(2)-10% H(2) at 300 degrees C for 1 h. PMID:19606339

  15. Toxicity of mercury and mercury compounds. (Latest citations from Pollution Abstracts). Published Search

    SciTech Connect

    Not Available

    1993-02-01

    The bibliography contains citations concerning the toxic effects of mercury and mercury compounds on biological systems. The citations examine mercury halides, organic mercury compounds, mercury metal, and mercury vapor. Metabolism, toxicology, occupational exposure, symptoms of exposure, mechanisms of interaction with biological systems, demographics of mercury accumulation and poisoning, and case reports are considered. Heavy metal pollution and bioaccumulation are referenced in related bibliographies. (Contains 250 citations and includes a subject term index and title list.)

  16. Effects of metal-soil contact time on the extraction of mercury from soils.

    PubMed

    Ma, Lan; Zhong, Huan; Wu, Yong-Gui

    2015-03-01

    To investigate the mercury aging process in soils, soil samples were spiked with inorganic mercury (Hg(II)) or methylated mercury (MeHg) and incubated for 2, 7, 14 or 28 days in the laboratory. Potential availability of mercury, assessed by bovine serum albumin (BSA) or calcium chloride (CaCl2) extraction, decreased by 2-19 times for Hg(II) or 2-6 times for MeHg, when the contact time increased from 2 to 28 days. Decreased Hg(II) extraction could be explained by Hg(II) geochemical fractionation, i.e., Hg(II) migrated from more mobile fractions (water soluble and stomach acid soluble fractions) to refractory ones (organo-complexed, strongly complexed and residual fractions) over time, resulting in more stable association of Hg(II) with soils. In addition, decrease of mercury extraction was more evident in soils with lower organic content in most treatments, suggesting that organic matter may potentially play an important role in mercury aging process. In view of the significant decreased Hg(II) or MeHg extraction with prolonged contact time, mercury aging process should be taken into account when assessing risk of mercury in contaminated soils. PMID:25613855

  17. Mercury in a spanish peat bog: archive of climate change and atmospheric metal deposition

    PubMed

    Martinez-Cortizas; Pontevedra-Pombal; Garcia-Rodeja; Novoa-Munoz; Shotyk

    1999-05-01

    A peat core from a bog in northwest Spain provides a record of the net accumulation of atmospheric mercury since 4000 radiocarbon years before the present. It was found that cold climates promoted an enhanced accumulation and the preservation of mercury with low thermal stability, and warm climates were characterized by a lower accumulation and the predominance of mercury with moderate to high thermal stability. This record can be separated into natural and anthropogenic components. The substantial anthropogenic mercury component began approximately 2500 radiocarbon years before the present, which is near the time of the onset of mercury mining in Spain. Anthropogenic mercury has dominated the deposition record since the Islamic period (8th to 11th centuries A.D.). The results shown here have implications for the global mercury cycle and also imply that the thermal lability of the accumulated mercury can be used not only to quantify the effects of human activity, but also as a new tool for quantitative paleotemperature reconstruction. PMID:10320369

  18. Behavior of metallic silver nanoparticles in a pilot wastewater treatment plant.

    PubMed

    Kaegi, Ralf; Voegelin, Andreas; Sinnet, Brian; Zuleeg, Steffen; Hagendorfer, Harald; Burkhardt, Michael; Siegrist, Hansruedi

    2011-05-01

    We investigated the behavior of metallic silver nanoparticles (Ag-NP) in a pilot wastewater treatment plant (WWTP) fed with municipal wastewater. The treatment plant consisted of a nonaerated and an aerated tank and a secondary clarifier. The average hydraulic retention time including the secondary clarifier was 1 day and the sludge age was 14 days. Ag-NP were spiked into the nonaerated tank and samples were collected from the aerated tank and from the effluent. Ag concentrations determined by inductively coupled plasma-mass spectrometry (ICP-MS) were in good agreement with predictions based on mass balance considerations. Transmission electron microscopy (TEM) analyses confirmed that nanoscale Ag particles were sorbed to wastewater biosolids, both in the sludge and in the effluent. Freely dispersed nanoscale Ag particles were only observed in the effluent during the initial pulse spike. X-ray absorption spectroscopy (XAS) measurements indicated that most Ag in the sludge and in the effluent was present as Ag(2)S. Results from batch experiments suggested that Ag-NP transformation to Ag(2)S occured in the nonaerated tank within less than 2 h. Physical and chemical transformations of Ag-NP in WWTPs control the fate, the transport and also the toxicity and the bioavailability of Ag-NP and therefore must be considered in future risk assessments. PMID:21466186

  19. Thermally Stable Silver Nanowires-Embedding Metal Oxide for Schottky Junction Solar Cells.

    PubMed

    Kim, Hong-Sik; Patel, Malkeshkumar; Park, Hyeong-Ho; Ray, Abhijit; Jeong, Chaehwan; Kim, Joondong

    2016-04-01

    Thermally stable silver nanowires (AgNWs)-embedding metal oxide was applied for Schottky junction solar cells without an intentional doping process in Si. A large scale (100 mm(2)) Schottky solar cell showed a power conversion efficiency of 6.1% under standard illumination, and 8.3% under diffused illumination conditions which is the highest efficiency for AgNWs-involved Schottky junction Si solar cells. Indium-tin-oxide (ITO)-capped AgNWs showed excellent thermal stability with no deformation at 500 °C. The top ITO layer grew in a cylindrical shape along the AgNWs, forming a teardrop shape. The design of ITO/AgNWs/ITO layers is optically beneficial because the AgNWs generate plasmonic photons, due to the AgNWs. Electrical investigations were performed by Mott-Schottky and impedance spectroscopy to reveal the formation of a single space charge region at the interface between Si and AgNWs-embedding ITO layer. We propose a route to design the thermally stable AgNWs for photoelectric device applications with investigation of the optical and electrical aspects. PMID:26971560

  20. Tunable white light emission in Parallel Tandem OLEDs made with silver metal as interlayer

    NASA Astrophysics Data System (ADS)

    Oliva, Jorge; Papadimitratos, Alexios; Zakhidov, Anvar; UT Dallas Team

    Parallel tandem organic light emitting diodes (OLEDs) which consisted in a top and bottom subunits, and joined with a thin layer of silver (interlayer) were fabricated. In this parallel tandem architecture the Ag metal is an active common anode, which permitted to inject holes into top and bottom subunits. Both subunits of the tandem can thus be connected functionally in a new geometry and addressed separately. Those Tandems had a yellow emitter (a mixture of MEH-PPV and TFB polymers) in the bottom subunit and a blue emitting molecule in the top subunit. The simultaneous combination of the emitted yellow and blue light when both subunits are operating produced white light. We could tune the white light from cool (CIE: 0.33, 0.25) to warm (CIE: 0.38, 0.39) by changing the intensity of the yellow light, that in turn depends on the ratio of MEH-PPV/TFB mixture used to make the emitting layer in the bottom subunit. We also compared the performance of the parallel tandem with these in series and we found additional advantages of the parallel architecture over the configuration for the series tandems such as: tunable chromaticity, lower turn on voltage (4V compared to 7V in the in-series tandem) and higher brightness. The best CIE coordinate we obtained for white light was (0.35, 0.35) which is near the ideal coordinate of (0.33,0.33).

  1. Quantitation of metal content in the silver-assisted growth of gold nanorods.

    PubMed

    Orendorff, Christopher J; Murphy, Catherine J

    2006-03-01

    The seed-mediated approach to making gold nanorods in aqueous surfactant solutions has become tremendously popular in recent years. Unlike the use of strong chemical reductants to make spherical gold nanoparticles, the growth of gold nanorods requires weak reducing conditions, leading to an unknown degree of gold reduction. The metal content of gold nanorods, made in high yield in the presence of silver ion, is determined by inductively coupled plasma atomic emission spectroscopy. Through the use of the known gold concentration in nanorods, molar extinction coefficients are calculated for nanorods of varying aspect ratios from 2.0 to 4.5. The extinction coefficients at the longitudinal plasmon band peak maxima for these nanorods vary from 2.5x10(9) to 5.5x10(9) M-1 cm-1, respectively, on a per-particle basis. Many of the gold ions present in the growth solution remain unreacted; insights into the growth mechanism of gold nanorods are discussed. PMID:16509687

  2. Electrochemiluminescent immunosensing of prostate-specific antigen based on silver nanoparticles-doped Pb (II) metal-organic framework.

    PubMed

    Ma, Hongmin; Li, Xiaojian; Yan, Tao; Li, Yan; Zhang, Yong; Wu, Dan; Wei, Qin; Du, Bin

    2016-05-15

    In this work, silver nanoparticles-doped Pb (II) metal-organic framework (Ag-MOF) was prepared and exploited as a luminescence probe for the development of label-free electrochemiluminescence (ECL) immunosensing scheme for prostate-specific antigen (PSA). The β-cyclodextrin based MOF, Pb-β-cyclodextrin (Pb(II)-β-CD) shows excellent ECL behavior and unexpected reducing capacity towards silver ions. Silver nanoparticles could massively form on the surface of Pb(II)-β-CD (Ag@Pb(II)-β-CD) without use any additional reducing agent, while the ECL behavior of Pb(II)-β-CD still was well retained. The Ag@Pb(II)-β-CD was used as a substrate material to modify glass carbon electrodes and formed a sensing platform for the fabricating ECL immunosensor. The presence of silver nanoparticles enables the facile immobilization of capturing antibody of PSA. The specific binding of PSA onto the electrode surface induces the decrease of ECL signals. A linear range of 0.001-50 ng mL(-1) with a detection limit of 0.34 pg mL(-1) (S/N=3) was obtained after the optimization of experimental conditions. This simply fabricated immunosensor exhibits good stability, accuracy and acceptable reproducibility, which suggesting its potential applications in clinical diagnostics. PMID:26735872

  3. What Do We Know of Childhood Exposures to Metals (Arsenic, Cadmium, Lead, and Mercury) in Emerging Market Countries?

    PubMed Central

    Horton, Lindsey M.; Mortensen, Mary E.; Iossifova, Yulia; Wald, Marlena M.; Burgess, Paula

    2013-01-01

    Arsenic, cadmium, lead, and mercury present potential health risks to children who are exposed through inhalation or ingestion. Emerging Market countries experience rapid industrial development that may coincide with the increased release of these metals into the environment. A literature review was conducted for English language articles from the 21st century on pediatric exposures to arsenic, cadmium, lead, and mercury in the International Monetary Fund's (IMF) top 10 Emerging Market countries: Brazil, China, India, Indonesia, Mexico, Poland, Russia, South Korea, Taiwan, and Turkey. Seventy-six peer-reviewed, published studies on pediatric exposure to metals met the inclusion criteria. The reported concentrations of metals in blood and urine from these studies were generally higher than US reference values, and many studies identified adverse health effects associated with metals exposure. Evidence of exposure to metals in the pediatric population of these Emerging Market countries demonstrates a need for interventions to reduce exposure and efforts to establish country-specific reference values through surveillance or biomonitoring. The findings from review of these 10 countries also suggest the need for country-specific public health policies and clinician education in Emerging Markets. PMID:23365584

  4. What do we know of childhood exposures to metals (arsenic, cadmium, lead, and mercury) in emerging market countries?

    PubMed

    Horton, Lindsey M; Mortensen, Mary E; Iossifova, Yulia; Wald, Marlena M; Burgess, Paula

    2013-01-01

    Arsenic, cadmium, lead, and mercury present potential health risks to children who are exposed through inhalation or ingestion. Emerging Market countries experience rapid industrial development that may coincide with the increased release of these metals into the environment. A literature review was conducted for English language articles from the 21st century on pediatric exposures to arsenic, cadmium, lead, and mercury in the International Monetary Fund's (IMF) top 10 Emerging Market countries: Brazil, China, India, Indonesia, Mexico, Poland, Russia, South Korea, Taiwan, and Turkey. Seventy-six peer-reviewed, published studies on pediatric exposure to metals met the inclusion criteria. The reported concentrations of metals in blood and urine from these studies were generally higher than US reference values, and many studies identified adverse health effects associated with metals exposure. Evidence of exposure to metals in the pediatric population of these Emerging Market countries demonstrates a need for interventions to reduce exposure and efforts to establish country-specific reference values through surveillance or biomonitoring. The findings from review of these 10 countries also suggest the need for country-specific public health policies and clinician education in Emerging Markets. PMID:23365584

  5. Electrochemical Reduction of Silver Vanadium Phosphorous Oxide, Ag2VO2PO4: Silver Metal Deposition and Associated Increase in Electrical Conductivity

    PubMed Central

    Marschilok, Amy C.; Kozarsky, Eric S.; Tanzil, Kevin; Zhu, Shali; Takeuchi, Kenneth J.; Takeuchi, Esther S.

    2010-01-01

    This report details the chemical and associated electrical resistance changes of silver vanadium phosphorous oxide (Ag2VO2PO4, SVPO) incurred during electrochemical reduction in a lithium based electrochemical cell over the range of 0 to 4 electrons per formula unit. Specifically the cathode electrical conductivities and associated cell DC resistance and cell AC impedance values vary with the level of reduction, due the changes of the SVPO cathode. Initially, Ag+ is reduced to Ag0 (2 electrons per formula unit, or 50% of the calculated theoretical value of 4 electrons per formula unit), accompanied by significant decreases in the cathode electrical resistance, consistent with the formation of an electrically conductive silver metal matrix within the SVPO cathode. As Ag+ reduction progresses, V5+ reduction initiates; once the SVPO reduction process progresses to where the reduction of V5+ to V4+ is the dominant process, both the cell and cathode electrical resistances then begin to increase. If the discharge then continues to where the dominant cathode reduction process is the reduction of V4+ to V3+, the cathode and cell electrical resistances then begin to decrease. The complex cathode electrical resistance pattern exhibited during full cell discharge is an important subject of this study. PMID:20657813

  6. Characteristics of some silver-, and base metal-bearing, epithermal deposits of Mexico and Peru

    USGS Publications Warehouse

    Foley, Nora K.

    1984-01-01

    Although many characteristics of the geology and geochemistry of this type of deposit were considered, the most important criterion for choosing these deposits was that they have substantial quantities of precious- and base-metal mineralization. Additional criteria for selecting the deposits were that they be hosted primarily by calc-alkaline volcanic rocks of intermediate to silicic composition and that they be younger than Tertiary in age. Many deposits in Mexico and Peru and other parts of Central and South America were excluded because the literature describing the districts is not readily available. Furthermore, many districts have not been examined in detail or the information available is of limited geological scope. The four districts that are compiled in this report were chosen because they are described in abundant literature dating from early mining reports on the general geology and mineralogy to very recent data on detailed geochemical and mineralogical studies. They were chosen as being fairly typical, classic examples of near-surface, low-temperature vein deposits as described by Lindgren (1928) in his treatise on ore deposits (Mineral deposits, McGraw-Hill, 1049 p.). These deposits are similar in aspects of their geology and geochemistry to many of the famous, epithermal silver mining districts in Colorado and Nevada including Creede, Colorado, Tonapah, Nevada, and the Sunnyside Mine of the Eureka district, Colorado, and, in the special case of Julcani, to Summitville, Colorado, and Goldfield, Nevada. The characteristics that distinguish them include overall size, production and alteration assemblage. The information documented in each summary will be used in a forthcoming series of papers on the comparative anatomy of precious and base metal deposits in North and South America.

  7. Detection of heavy metals (Cu+2, Hg+2) by biosynthesized silver nanoparticles

    NASA Astrophysics Data System (ADS)

    Maiti, Swarnali; Barman, Gadadhar; Konar Laha, Jayasree

    2016-04-01

    Here, we are reporting two methods for detection of Cu+2 ion and Hg+2 ions using biosynthesized silver nanoparticles. The detection of Cu+2 ion was based on changes in absorbance resulting from complex formation of the metal ion. Various concentrations of Cu+2 ion were used to test the linearity and sensitivity of the method. A new peak at around 770 nm, in addition to the peak of the AgNP at 406 nm, was observed in each case (above 20 µM). With the increase of concentration of Cu+2 ion solution, the absorbance at 406 nm peak decreased and that of 770 nm increased gradually. The calibration curve obtained from the ratio of the absorption coefficients of these two peaks (Ex770/406) versus concentration of Cu+2 ions enables one to estimate quantitatively the amount of Cu+2 ions present in water in µM levels. This AgNP was further functionalized with 3-mercapto-1, 2-propanediol (MPD) for detection of Hg+2 present in water by colorimetric method. As soon as Hg+2 solution was added in MPD-functionalized AgNP (MPD-AgNP), a new peak at around 606 nm appeared along with the peak at 404 nm. The new peak might be due to the aggregations occurred by the recognition of heavy metal ion Hg+2 by MPD-AgNP through dipropionate ion. A calibration curve between the ratios of the absorption coefficients of these two peaks (Ex404/606) and concentration of Hg+2 was drawn for quantitative estimation of Hg+2 present in water at µM level.

  8. Metallogenesis of Gold and Silver in Northeast Russia

    NASA Astrophysics Data System (ADS)

    Gamyanin, G. N.; Goryachev, N. A.

    2004-12-01

    Three genetic series of ore lode deposit types in Notheast Russia are distinguished: hydrothermal-metamorphogenic (early collision stage), hydrothermal plutonogenic granitoid (late collisional stage), and volcanogenic (post-collisional stage). Metallogenesis in the hydrothermal-metamorphogenic series is more or less exclusively gold mineralization (gold-quartz veins, and disseminated gold-sulfide mineralization). In the Yana-Kolyma metallogenic belt, gold mineralization of this genetic type occurs as lenticular quartz bodies. In the Allakh-Yun and West Verkhoyansk belts it is present as zones of stratified quartz veins. The hydrothermal-plutonogenic lode deposits related to granitoid suites were produced by ore-magmatic systems (OMS) with similar geochemical specialization for gold that most probably had a palingenetic crustal origin (Rb-Sr and Pb isotopic data). As the collision proceeded, large granitoid plutons were emplaced to form extensive belts (150-140 and 130-120 Ma), within which local ore-magmatic fields were formed. The intermediate-depth magmatic chambers (15-18 km depth) of the OMSs generated the low-sulfide gold-quartz lode deposits, while in hypabyssal magmatic chambers (1-2 km depth) granitoid-related gold lode deposits are produced. The volcanogenic series of shallow-depth ore lode types are silver-base metal, gold-silver-antimony, and silver-mercury. Subduction processes occurring along the Okhotsk active continental margin could have reactivated the earlier strike-slip fault zones, which served as the ore-controlling structures for the development of Late Cretaceous (95-70 Ma) subvolcanic magmatism and the formation of diversified mineralization (silver-base metal, gold-silver-antimony, and silver-mercury). The earliest is silver-base metal mineralization associated with subvolcanic granite porphyries and located in tin ore fields, thus confirming our supposition about the activation of deep horizons of staniferous OMSs. Gold-silver-antimony and

  9. Ecological and water quality impairment resulting from the New Idria Mercury Mine and natural sources in the San Carlos and Silver Creek watersheds, central California

    NASA Astrophysics Data System (ADS)

    Rytuba, J. J.; Hothem, R.; Goldstein, D.; Brussee, B.

    2011-12-01

    The New Idria Mercury Mine in central California is the second largest mercury (Hg) deposit in North America and has been proposed as a US EPA Superfund Site based on ecological impairment to the San Carlos and Silver Creek watersheds. Water, sediment, and biota were sampled in San Carlos Creek in the mine area and downstream for 25 km into the watershed termed Silver Creek. Release of acid rock drainage (ARD) and erosion of mine tailings have impacted the watershed during 120 years of mining and since the mine was closed in 1972. The watershed can be divided into three segments based on water and sediment composition, Hg sources and concentrations, and biodiversity of aquatic invertebrates. Creek waters in segment no. 1 above the mine area consist of Mg-Ca-CO3 meteoric water with pH 8.73. Hg concentrations are elevated in both sediment (100μg/g), and in waters (60 ng/L) because of erosion of Hg mine tailings in the upper part of the watershed. Invertebrate biodiversity is the highest of the sites sampled in the watershed, with seven families (six orders) of aquatic invertebrates collected and six other families observed. In the mine area isotopically heavy ARD (pH 2.7) with high levels of Fe(II), SO4, and total Hg (HgT: 76.7 ng/L) enters and mixes with meteoric creek water, constituting from 10-15% of the water in the 10-km long second creek segment downstream from the mine. Oxidation of Fe(II) from ARD results in precipitation of FeOOH which is transported and deposited as an Fe precipitate that has high Hg and MMeHg concentration (Hg: 15.7-79 μg/g, MMeHg: 0.31 - 1.06 ng/g). Concentrations of HgT are uniformly high (1530-2890 ng/L) with particulate Hg predominant. MMeHg ranges from 0.21-0.99 ng/L. In the area just downstream from the ARD source, biodiversity of invertebrates was low, with only one taxa (water striders) available in sufficient numbers and mass (> 1 g)_to be sampled. Biodiversity further downstream was also low, with only up to 2 families present

  10. Partitioning of U, Th and K Between Metal, Sulfide and Silicate, Insights into the Volatile-Content of Mercury

    NASA Technical Reports Server (NTRS)

    Habermann, M.; Boujibar, A.; Righter, K.; Danielson, L.; Rapp, J.; Righter, M.; Pando, K.; Ross, D. K.; Andreasen, R.; Chidester, B.

    2016-01-01

    During the early stages of the Solar System formation, especially during the T-Tauri phase, the Sun emitted strong solar winds, which are thought to have expelled a portion of the volatile elements from the inner solar system. It is therefore usually believed that the volatile depletion of a planet is correlated with its proximity to the Sun. This trend was supported by the K/Th and K/U ratios of Venus, the Earth, and Mars. Prior to the MESSENGER mission, it was expected that Mercury is the most volatile-depleted planet. However, the Gamma Ray Spectrometer of MESSENGER spacecraft revealed elevated K/U and K/Th ratios for the surface of Mercury, much higher than previous expectations. It is possible that the K/Th and K/U ratios on the surface are not a reliable gauge of the bulk volatile content of Mercury. Mercury is enriched in sulfur and is the most reduced of the terrestrial planets, with oxygen fugacity (fO2) between IW-6.3 and IW-2.6 log units. At these particular compositions, U, Th and K behave differently and can become more siderophile or chalcophile. If significant amounts of U and Th are sequestered in the core, the apparent K/U and K/Th ratios measured on the surface may not represent the volatile budget of the whole planet. An accurate determination of the partitioning of these elements between silicate, metal, and sulfide phases under Mercurian conditions is therefore essential to better constrain Mercury's volatile content and assess planetary formation models.

  11. Method for the recovery of silver from silver zeolite

    SciTech Connect

    Reimann, George A.

    1986-01-01

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

  12. Method for the recovery of silver from silver zeolite

    DOEpatents

    Reimann, G.A.

    1985-03-05

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

  13. Method and apparatus for sampling atmospheric mercury

    DOEpatents

    Trujillo, Patricio E.; Campbell, Evan E.; Eutsler, Bernard C.

    1976-01-20

    A method of simultaneously sampling particulate mercury, organic mercurial vapors, and metallic mercury vapor in the working and occupational environment and determining the amount of mercury derived from each such source in the sampled air. A known volume of air is passed through a sampling tube containing a filter for particulate mercury collection, a first adsorber for the selective adsorption of organic mercurial vapors, and a second adsorber for the adsorption of metallic mercury vapor. Carbon black molecular sieves are particularly useful as the selective adsorber for organic mercurial vapors. The amount of mercury adsorbed or collected in each section of the sampling tube is readily quantitatively determined by flameless atomic absorption spectrophotometry.

  14. UV fragmentation and ultrafast dynamics of trinuclear silver/1-methylthymine and silver/1-methyluracil metal-base pairs in an ion trap

    NASA Astrophysics Data System (ADS)

    Nosenko, Yevgeniy; Riehn, Christoph; Klopper, Wim

    2016-08-01

    We report on gas phase UV action spectroscopy and photodynamics of [Ag3(1MT-H/1MU-H)2]+ comprised of a linear silver string and two deprotonated 1-methyl-thymine/uracil (1MT/1MU) ligands. We applied pump-probe femtosecond laser photofragmentation in an electrospray ion trap mass spectrometer and high-level ab initio calculations at the level of approximate coupled-cluster singles-doubles theory. The experimental UV band at 283/275 nm is assigned to a red shifted 1ππ∗ nucleobase located transition. Relaxation of the 1ππ∗ state occurs with time constants of 0.2/1.1 ps and 0.2/4.2 ps for the 1MT and 1MU complexes, respectively, on a similar ultrafast time scale as non-metalated uracil derivatives.

  15. Detection of mercury ions using silver telluride nanoparticles as a substrate and recognition element through surface-enhanced Raman scattering

    PubMed Central

    Wang, Chia-Wei; Lin, Zong-Hong; Roy, Prathik; Chang, Huan-Tsung

    2013-01-01

    In this paper we unveil a new sensing strategy for sensitive and selective detection of Hg2+ through surface-enhanced Raman scattering (SERS) using Ag2Te nanoparticles (NPs) as a substrate and recognition element and rhodamine 6G (R6G) as a reporter. Ag2Te NPs prepared from tellurium dioxide and silver nitrate and hydrazine in aqueous solution containing sodium dodecyl sulfate at 90°C with an average size of 26.8 ± 4.1 nm (100 counts) have strong SERS activity. The Ag2Te substrate provides strong SERS signals of R6G with an enhancement factor of 3.6 × 105 at 1360 cm−1, which is comparable to Ag NPs. After interaction of Ag2Te NPs with Hg2+, some HgTe NPs are formed, leading to decreases in the SERS signal of R6G, mainly because HgTe NPs relative to Ag2Te NPs have weaker SERS activity. Under optimum conditions, this SERS approach using Ag2Te as substrates is selective for the detection of Hg2+, with a limit of detection of 3 nM and linearity over 10–150 nM. The practicality of this approach has been validated for the determination of the concentrations of spiked Hg2+ in a pond water sample. PMID:24790948

  16. Metal-Silicate-Sulfide Partitioning of U, Th, and K: Implications for the Budget of Volatile Elements in Mercury

    NASA Technical Reports Server (NTRS)

    Habermann, M.; Boujibar, A.; Righter, K.; Danielson, L.; Rapp, J.; Righter, M.; Pando, K.; Ross, D. K.; Andreasen, R.

    2016-01-01

    During formation of the solar system, the Sun produced strong solar winds, which stripped away a portion of the volatile elements from the forming planets. Hence, it was expected that planets closest to the sun, such as Mercury, are more depleted in volatile elements in comparison to other terrestrial planets. However, the MESSENGER mission detected higher than expected K/U and K/Th ratios on Mercury's surface, indicating a volatile content between that of Mars and Earth. Our experiments aim to resolve this discrepancy by experimentally determining the partition coefficients (D(sup met/sil)) of K, U, and Th between metal and silicate at varying pressure (1 to 5 GPa), temperature (1500 to 1900 C), oxygen fugacity (IW-2.5 to IW-6.5) and sulfur-content in the metal (0 to 33 wt%). Our data show that U, Th, and K become more siderophile with decreasing fO2 and increasing sulfur-content, with a stronger effect for U and Th in comparison to K. Using these results, the concentrations of U, Th, and K in the bulk planet were calculated for different scenarios, where the planet equilibrated at a fO2 between IW-4 and IW-7, assuming the existence of a FeS layer, between the core and mantle, with variable thickness. These models show that significant amounts of U and Th are partitioned into Mercury's core. The elevated superficial K/U and K/Th values are therefore only a consequence of the sequestration of U and Th into the core, not evidence of the overall volatile content of Mercury.

  17. Fundamental mechanisms of oxidation of alkaline earth-bearing metal precursors: yttrium-barium-copper-silver-palladium and silver bariate

    NASA Astrophysics Data System (ADS)

    Sitaraman, Vilayannur R.

    Noble-metal-bearing metallic precursors can be selectively oxidized to yield oxide/noble metal composites. This processing method is investigated for producing 123/Ag-Pd laminates from a solid metallic Y-Ba-Cu-Ag-Pd precursor. A unique feature heretofore unnoticed is the external oxidation mechanism of Ba. The extent of external oxidation at 840C in a 3%H2-Ar atmosphere (PO2 ˜ 10-19 atm.) as measured by a segregation factor, is higher for Ba than for Y. Combined with the fact that Ba does not have significant solid solubility in Ag, Cu or Pd, this means that a short circuit transport path is possible for transport of Ba through such metals as described in chapter 1. Since diffusion through grain boundaries, is fast, the effective permeability of Ba can be relatively high even though its solubility is low. This proposed mechanism is proven using a model system, the Ag5Ba intermetallic compound. Both internal and external oxidation has been demonstrated in this material. Grain boundary diffusion is demonstrated using Ag clad Ag 5Ba. Due to a change in the mechanism from external to internal oxidation of Y in Y-Ba-Cu-Ag-Pd alloys, the imbalance in the surface stoichiometry caused by Ba segregation is not easily removed. A mechanism proposed by Meijering for copper oxide dissolution, Cu migration and Cu reoxidation at the outer surface is also consistent with the microstructural observations in oxidized Y-Ba-Cu-Ag-Pd specimens.

  18. [Spatial distribution and ecological significance of heavy metals in soils from Chatian mercury mining deposit, western Hunan province].

    PubMed

    Sun, Hong-Fei; Li, Yong-Hu; Ji, Yan-Fang; Yang, Lin-Sheng; Wang, Wu-Yi

    2009-04-15

    Ores, waste tailings and slag, together with three typical soil profiles (natural soil profiles far from mine entrance and near mine entrance, soil profile under slag) in Chatian mercury mining deposit (CMD), western Hunan province were sampled and their concentrations of mercury (Hg), arsenic (As), lead (Pb), cadmium (Cd), zinc (Zn) were determined by HG-ICP-AES and ICP-MS. Enrichment factor and correlation analysis were taken to investigate the origins, distribution and migration of Hg, as well as other heavy metals in the CMD. The results show that Hg is enriched in the bottom of the soil profile far from mine entrance but accumulated in the surface of soil profiles near mine entrance and under slag. The soil profiles near mine entrance and under slag are both contaminated by Hg, while the latter is contaminated more heavily. In the soil profile under slag, Hg concentration in the surface soil, Hg average concentration in the total profile, and the leaching depth of soil Hg are 640 microg x g(-1), (76.74 +/- 171.71) microg x g(-1), and more than 100 cm, respectively; while 6.5 microg x g(-1), (2.74 +/- 1.90) microg x g(-1), and 40 cm, respectively, are found in the soil profile near mine entrance. Soil in the mercury mine area is also polluted by Cd, As, Pb, Zn besides metallogenic element Hg, among which Cd pollution is relatively heavier than others. The mobility of the studied heavy metals in soil follows the order as Hg > Cd > As > Zn approximately equal to Pb. The leaching depth of the heavy metals is influenced by total concentration in the surface soil and soil physico-chemical parameters. The origins, distribution and migration of heavy metals in soil profile in the mining area are related to primary geological environment, and strongly influenced by human mining activities. PMID:19545023

  19. Got Mercury?

    NASA Technical Reports Server (NTRS)

    Meyers, Valerie; James, John T.; McCoy, Torin; Garcia, Hector

    2010-01-01

    Many lamps used in various spacecraft contain elemental mercury, which is efficiently absorbed through the lungs as a vapor. The liquid metal vaporizes slowly at room temperature, but may be completely vaporized when lamps are operating. Because current spacecraft environmental control systems are unable to remove mercury vapors, we considered short-term and long-term exposures. Using an existing study, we estimated mercury vapor releases from lamps that are not in operation during missions lasting less than or equal to 30 days; whereas we conservatively assumed complete vaporization from lamps that are operating or being used during missions lasing more than 30 days. Based on mercury toxicity, the Johnson Space Center's Toxicology Group recommends stringent safety controls and verifications for any hardware containing elemental mercury that could yield airborne mercury vapor concentrations greater than 0.1 mg/m3 in the total spacecraft atmosphere for exposures lasting less than or equal to 30 days, or concentrations greater than 0.01 mg/m3 for exposures lasting more than 30 days.

  20. 1. View looking south on Montana Street. The Silver Bow ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    1. View looking south on Montana Street. The Silver Bow County Courthouse (1910-1912) is on the left. - Butte Historic District, Bounded by Copper, Arizona, Mercury & Continental Streets, Butte, Silver Bow County, MT

  1. Mercury, monomethyl mercury, and dissolved organic carbon concentrations in surface water entering and exiting constructed wetlands treated with metal-based coagulants, Twitchell Island, California

    USGS Publications Warehouse

    Stumpner, Elizabeth B.; Kraus, Tamara E.C.; Fleck, Jacob A.; Hansen, Angela M.; Bachand, Sandra M.; Horwath, William R.; DeWild, John F.; Krabbenhoft, David P.; Bachand, Philip A.M.

    2015-01-01

    Following coagulation, but prior to passage through the wetland cells, coagulation treatments transferred dissolved mercury and carbon to the particulate fraction relative to untreated source water: at the wetland cell inlets, the coagulation treatments decreased concentrations of filtered total mercury by 59–76 percent, filtered monomethyl mercury by 40–70 percent, and dissolved organic carbon by 65–86 percent. Passage through the wetland cells decreased the particulate fraction of mercury in wetland cells that received coagulant-treated water. Changes in total mercury, monomethyl mercury, and dissolved organic carbon concentrations resulting from wetland passage varied both by treatment and season. Despite increased monomethyl mercury in the filtered fraction during wetland passage between March and August, the coagulation-wetland systems generally decreased total mercury (filtered plus particulate) and monomethyl mercury (filtered plus particulate) concentrations relative to source water. Coagulation—either alone or in association with constructed wetlands—could be an effective way to decrease concentrations of mercury and dissolved organic carbon in surface water as well as the bioavailability of mercury in the Sacramento–San Joaquin Delta.

  2. Impact of effective volume ratio of a dispersant to silver nano-particles on silicon solar cell efficiency in direct ink-jet metallization

    NASA Astrophysics Data System (ADS)

    Shin, Dong-Youn; Cha, Yong-Kee; Ryu, Han-Hee; Kim, Sang-Ho

    2012-11-01

    In this study, the direct ink-jet metallization of finger electrodes on a multi-crystalline silicon solar cell is attempted and the impact of the silver particle size on solar cell efficiency is investigated using silver nano-inks with two different silver particle sizes. When the silver particle size approaches the nano-metric regime of around 18.1 nm, the solar cell efficiency is as low as 8.6%. On the other hand, the solar cell efficiency increases up to a maximum of 12.1% using silver particles that are around 180 nm in size. It is found that the dependence of the solar cell efficiency on the silver particle size is related to the effective volume ratio of a dispersant to silver. As the effective volume ratio increases, detrimental effects, such as an explosive decomposition of the dispersant and high residual stress due to the high volumetric shrinkage of a direct ink-jet printed finger electrode, result in poor contact formation which eventually leads to poor solar cell efficiency. With these experimental results, potential development directions for an ink-jet printer for the direct metallization of a silicon solar cell are comprehensively discussed.

  3. DNA derived fluorescent bio-dots for sensitive detection of mercury and silver ions in aqueous solution

    NASA Astrophysics Data System (ADS)

    Song, Ting; Zhu, Xuefeng; Zhou, Shenghai; Yang, Guang; Gan, Wei; Yuan, Qunhui

    2015-08-01

    Inspired by the high affinity between heavy metal ions and bio-molecules as well as the low toxicity of carbon-based quantum dots, we demonstrated the first application of a DNA derived carbonaceous quantum dots, namely bio-dots, in metal ion sensing. The present DNA-derived bio-dots contain graphitic carbon layers with 0.242 nm lattice fringes, exhibit excellent fluorescence property and can be obtained via a facile hydrothermal preparation procedure. Hg(II) and Ag(I) are prone to be captured by the bio-dots due to the existence of residual thymine (T) and cytosine (C) groups, resulting in a quenched fluorescence while other heavy metal ions would cause negligible changes on the fluorescent signals of the bio-dots. The bio-dots could be used as highly selective toxic-free biosensors, with two detecting linear ranges of 0-0.5 μM and 0.5-6 μM for Hg(II) and one linear range of 0-10 μM for Ag(I). The detection limits (at a signal-to-noise ratio of 3) were estimated to be 48 nM for Hg(II) and 0.31 μM for Ag(I), respectively. The detection of Hg(II) and Ag(I) could also be realized in the real water sample analyses, with satisfying recoveries ranging from 87% to 100%.

  4. Effect of cropping systems on heavy metal distribution and mercury fractionation in the Wanshan mining district, China: implications for environmental management.

    PubMed

    Wang, Jianxu; Feng, Xinbin; Anderson, Christopher W N; Qiu, Guangle; Bao, Zhengduo; Shang, Lihai

    2014-09-01

    The authors studied the concentration of heavy metals and mercury fractionation in contaminated soil in 2 agricultural land use systems (paddy rice and dry land) at the Wanshan mercury mine in China. The average concentrations of chromium, lead, copper, nickel, and zinc were generally lower in paddy rice soil relative to corn field soil. Soil under corn field production was slightly contaminated with lead (22-100 mg/kg), copper (31-64 mg/kg), and nickel (22-76 mg/kg) and moderately contaminated with zinc (112-635 mg/kg). In both soils, correlation of these metals with the titanium concentration in the soil indicates a geogenic origin for each metal (lead, r = 0.48; copper, r = 0.63; nickel, r = 0.47; zinc, r = 0.48). The mercury and antimony concentration in soil was high under both cropping systems, and future remediation efforts should consider the potential environmental risk presented by these metals. The concentration of bioavailable mercury in soil ranged from 0.3 ng/g to 11 ng/g across the 2 cropping systems. The majority of mercury (>80%) was associated with organic matter and the residual fraction. However, soil under paddy rice production exhibited a significantly lower concentration of Fe/Mn oxide-bound mercury than that under corn field production. This may be a function of the reduction of Fe/Mn oxides in the paddy rice soil, with the subsequent release of adsorbed metals to the soil solution. Sequential change from corn field to paddy rice production, as practiced in Wanshan, should therefore be avoided. Mercury adsorbed to Fe/Mn oxides in corn field soil potentially could be released into the soil solution and be made available for biomethylation under the flooded water management conditions of a rice paddy. PMID:24924832

  5. Distribution of dissolved silver in marine waters

    NASA Astrophysics Data System (ADS)

    Barriada, J. L.; Achterberg, E. P.; Tappin, A.; Truscott, J.

    2003-04-01

    Silver is one of the most toxic heavy metals, surpassed only by mercury [1-3]. Monitoring of dissolved silver concentrations in natural waters is therefore of great importance. The determination of dissolved silver in waters is not without challenges, because of its low (picomolar) concentrations. Consequently, there are only a few reported studies in marine waters, which have been performed in USA [4-6] and Japan [7]. The analytical techniques used in the reported studies for the determination of silver in seawater were Graphite Furnace Atomic Absorption Spectroscopy (GFAAS) after solvent extraction [2,4,5], and Inductively Coupled Plasma Mass Spectrometry (ICP-MS) after solvent extraction or solid phase extraction [7,8]. In this contribution, we will present an optimised Magnetic Sector (MS) ICP-MS technique for the determination of dissolved silver in marine waters. The MS-ICP-MS method used anion exchange column to preconcentrate silver from saline waters, and to remove the saline matrix. The ICP-MS method has been used successfully to determine total dissolved silver in estuarine and oceanic samples. Bibliography 1. H. T. Ratte, Environ. Toxicol. Chem. 1999, 18: p. 89-108. 2. R. T. Herrin, A. W. Andren and D. E. Armstrong, Environ. Sci. Technol. 2001, 35: 1953-1958. 3. D. E. Schildkraut, P. T. Dao, J. P. Twist, A. T. Davis and K. A. Robillard, Environ. Toxicol. Chem. 1998, 17: 642-649. 4. E. Breuer, S. A. Sanudo-Wilhelmy and R. C. Aller, Estuaries. 1999, 22:603-615. 5. A. R. Flegal, S. A. Sanudowilhelmy and G. M. Scelfo, Mar. Chem. 1995, 49: 315-320. 6. S. N. Luoma, Y. B. Ho and G. W. Bryan, Mar. Pollut. Bull. 1995, 31: 44-54. 7. Y. Zhang, H. Amakawa and Y. Nozaki, Mar. Chem. 2001, 75: 151-163. 8. L. Yang and R. E. Sturgeon, J. Anal. At. Spectrom. 2002, 17: 88-93.

  6. A sensitive and selective sensing platform based on CdTe QDs in the presence of l-cysteine for detection of silver, mercury and copper ions in water and various drinks.

    PubMed

    Gong, Tingting; Liu, Junfeng; Liu, Xinxin; Liu, Jie; Xiang, Jinkun; Wu, Yiwei

    2016-12-15

    Water soluble CdTe quantum dots (QDs) have been prepared simply by one-pot method using potassium tellurite as stable tellurium source and thioglycolic acid (TGA) as stabilizer. The fluorescence of CdTe QDs can be improved 1.3-fold in the presence of l-cysteine (Cys), however, highly efficiently quenched in the presence of silver or mercury or copper ions. A sensitive and selective sensing platform for analysis of silver, mercury and copper ions has been simply established based on CdTe QDs in the presence of l-cysteine. Under the optimum conditions, excellent linear relationships exist between the quenching degree of the sensing platform and the concentrations of Ag(+), Hg(2+) and Cu(2+) ranging from 0.5 to 40ngmL(-1). By using masking agents of sodium diethyldithiocarbamate (DDTC) for Ag(+) and Cu(2+), NH4OH for Ag(+) and Hg(2+) and 1-(2-Pyridylazo)-2-naphthol (PAN) for Hg(2+) and Cu(2+), Hg(2+), Cu(2+) and Ag(+) can be exclusively detected in coexistence with other two ions, and the detection limits (3σ) were 0.65, 0.063 and 0.088ngmL(-1) for Ag(+), Hg(2+) and Cu(2+), respectively. This effective sensing platform has been used to detection of Ag(+), Hg(2+) and Cu(2+) in water and various drinks with satisfactory results. PMID:27451185

  7. In situ fabrication of silver nanoparticle-filled hydrogen titanate nanotube layer on metallic titanium surface for bacteriostatic and biocompatible implantation

    PubMed Central

    Wang, Zheng; Sun, Yan; Wang, Dongzhou; Liu, Hong; Boughton, Robert I

    2013-01-01

    A silver nanoparticle (AgNP)-filled hydrogen titanate nanotube layer was synthesized in situ on a metallic titanium substrate. In the synthesis approach, a layer of sodium titanate nanotubes is first prepared on the titanium surface by using a hydrothermal method. Silver nitrate solution is absorbed into the nanotube channels by immersing a dried nanotube layer in silver nitrate solution. Finally, silver ions are reduced by glucose, leading to the in situ growth of AgNPs in the hydrogen titanate nanotube channels. Long-term silver release and bactericidal experiments demonstrated that the effective silver release and effective antibacterial period of the titanium foil with a AgNP-filled hydrogen titanate nanotube layer on the surface can extend to more than 15 days. This steady and prolonged release characteristic is helpful to promote a long-lasting antibacterial capability for the prevention of severe infection after surgery. A series of antimicrobial and biocompatible tests have shown that the sandwich nanostructure with a low level of silver loading exhibits a bacteriostatic rate as high as 99.99%, while retaining low toxicity for cells and possessing high osteogenic potential. Titanium foil with a AgNP-filled hydrogen titanate nanotube layer on the surface that is fabricated with low-cost surface modification methods is a promising implantable material that will find applications in artificial bones, joints, and dental implants. PMID:23966780

  8. Silver Ions in Non-canonical DNA Base Pairs: Metal-Mediated Mismatch Stabilization of 2'-Deoxyadenosine and 7-Deazapurine Derivatives with 2'-Deoxycytidine and 2'-Deoxyguanosine.

    PubMed

    Yang, Haozhe; Seela, Frank

    2016-09-01

    Novel silver-mediated dA-dC, dA*-dC, and dA*-dG base pairs were formed in a natural DNA double helix environment (dA* denotes 7-deaza-dA, 7-deaza-7-iodo-dA, and 7-cyclopropyl-7-deaza-dA). 7-Deazapurine nucleosides enforce silver ion binding and direct metal-mediated base pair formation to their Watson-Crick face. New phosphoramidites were prepared from 7-deaza-dA, 7-deaza-7-iodo-dA, and 7-cyclopropyl-7-deaza-dA, which contain labile isobutyryl protecting groups. Solid-phase synthesis furnished oligonucleotides that contain mismatches in near central positions. Increased thermal stabilities (higher Tm values) were observed for oligonucleotide duplexes with non-canonical dA*-dC and dA-dC pairs in the presence of silver ions. The stability of the silver-mediated base pairs was pH dependent. Silver ion binding was not observed for the dA-dG mismatch but took place when mismatches were formed between 7-deazaadenine and guanine. The specific binding of silver ions was confirmed by stoichiometric UV titration experiments, which proved that one silver ion is captured by one mismatch. The stability increase of canonical DNA mismatches might have an impact on cellular DNA repair. PMID:27492501

  9. Treatment of Mercury Contaminated Oil from Sandia National Laboratory

    SciTech Connect

    Klasson, KT

    2002-05-28

    First Article Tests of a stabilization method for greater than 260 mg mercury/kg oil were performed under a treatability study. This alternative treatment technology will address treatment of U.S. Department of Energy (DOE) organics (mainly used pump oil) contaminated with mercury and other heavy metals. Some of the oil is also co-contaminated with tritium, other radionuclides, and hazardous materials. The technology is based on contacting the oil with a sorbent powder (Self-Assembled Mercaptan on Mesoporous Support, SAMMS), proven to adsorb heavy metals, followed by stabilization of the oil/powder mixture using a stabilization agent (Nochar N990). Two variations of the treatment technology were included in the treatability study. The SAMMS (Self-Assembled Mercaptan on Mesoporous Silica) technology was developed by the Pacific Northwest National Laboratory for removal and stabilization of RCRA metals (i.e., lead, mercury, cadmium, silver, etc.) and for removal of mercury from organic solvents [1]. The SAMMS material is based on self-assembly of functionalized monolayers on mesoporous oxide surfaces. The unique mesoporous oxide supports provide a high surface area, thereby enhancing the metal-loading capacity. SAMMS material has high flexibility in that it binds with different forms of mercury, including metallic, inorganic, organic, charged, and neutral compounds [1] The material removes mercury from both organic wastes, such as pump oils, and from aqueous wastes. Mercury-loaded SAMMS not only passes TCLP tests, but also has good long-term durability as a waste form because: (1) the covalent binding between mercury and SAMMS has good resistance in ion-exchange, oxidation, and hydrolysis over a wide pH range and (2) the uniform and small pore size of the mesoporous silica prevents bacteria from solubilizing the bound mercury. Nochar's N990 Petrobond (Nochar, Inc., Indianapolis, IN) is an oil stabilization agent, specifically formulated for stabilizing vacuum pump

  10. Historical reconstruction of major pollutant levels in the Hudson-Raritan Basin: 1880-1980. Volume 2. Heavy metals and fossil fuels. Technical memo

    SciTech Connect

    Ayers, R.U.; Ayers, L.W.

    1988-10-01

    Volume 2: Metals covers the sources, production processes, consumptive uses of and environmental emissions of eight heavy metals (silver, arsenic, cadmium, chromium, copper, mercury, lead, zinc). Included are sections that discuss the part fossil fuel combustion plays in the overall pollution loading of Hudson-Raritan Basin.