Geology of the epithermal Ag-Au Huevos Verdes vein system and San José district, Deseado massif, Patagonia, Argentina

Science.gov (United States)

Dietrich, Andreas; Gutierrez, Ronald; Nelson, Eric P.; Layer, Paul W.

2012-03-01

The San José district is located in the northwest part of the Deseado massif and hosts a number of epithermal Ag-Au quartz veins of intermediate sulfidation style, including the Huevos Verdes vein system. Veins are hosted by andesitic rocks of the Bajo Pobre Formation and locally by rhyodacitic pyroclastic rocks of the Chon Aike Formation. New 40Ar/39Ar constraints on the age of host rocks and mineralization define Late Jurassic ages of 151.3 ± 0.7 Ma to 144.7 ± 0.1 Ma for volcanic rocks of the Bajo Pobre Formation and of 147.6 ± 1.1 Ma for the Chon Aike Formation. Illite ages of the Huevos Verdes vein system of 140.8 ± 0.2 and 140.5 ± 0.3 Ma are 4 m.y. younger than the volcanic host rock unit. These age dates are among the youngest reported for Jurassic volcanism in the Deseado massif and correlate well with the regional context of magmatic and hydrothermal activity. The Huevos Verdes vein system has a strike length of 2,000 m, with several ore shoots along strike. The vein consists of a pre-ore stage and three main ore stages. Early barren quartz and chalcedony are followed by a mottled quartz stage of coarse saccharoidal quartz with irregular streaks and discontinuous bands of sulfide-rich material. The banded quartz-sulfide stage consists of sulfide-rich bands alternating with bands of quartz and bands of chlorite ± illite. Late-stage sulfide-rich veinlets are associated with kaolinite gangue. Ore minerals are argentite and electrum, together with pyrite, sphalerite, galena, chalcopyrite, minor bornite, covellite, and ruby silver. Wall rock alteration is characterized by narrow (propylitic alteration. Gangue minerals are dominantly massive quartz intergrown with minor to accessory adularia. Epidote, illite, illite/smectite, and, preferentially at deeper levels, Fe-chlorite gangue indicate near-neutral pH hydrothermal fluids at temperatures of >220°C. Kaolinite occurring with the late sulfide-rich veinlet stage indicates pH 315°, whereas strike

A mineral quantification method for wall rocks at open pit mines, and application to the Martha Au-Ag mine, Waihi, New Zealand

International Nuclear Information System (INIS)

Castendyk, Devin N.; Mauk, Jeffrey L.; Webster, Jenny G.

2005-01-01

Pit lakes that result from open pit mining are potential water resources or potential environmental problems, depending on lake water quality. Wall rock mineralogy can affect lake chemistry if surface water inputs and/or groundwater inputs and/or lake water in contact with submerged wall rocks react with the wall rock minerals. This study presents a mineral quantification method to measure the distribution and concentration of wall rock minerals in open pit mines, and applies the method to the Martha epithermal Au-Ag mine, Waihi, New Zealand. Heterogeneous ore deposits, like Martha, require a large number of wall rock samples to accurately define mineral distributions. X-ray diffraction analyses of 125 wall rock samples identified the most abundant minerals in the wall rocks as quartz, adularia, albite, illite, chlorite, kaolinite, pyrite and calcite. Distribution maps of these minerals defined 8 relatively homogenous areas of wall rock referred to as 'mineral associations': weakly-altered, propylitic, fresh-argillic, weathered-argillic, oxidized, potassic, quartz veins, and post-mineralization deposits. X-ray fluorescence, Leco furnace, and neutron activation analyses of 46 representative samples produced the geochemical dataset used to assign quantities of elements to observed minerals, and to calculate average mineral concentrations in each association. Thin-section petrography and calcite concentrations from Sobek acid-digestions confirm the calculated mineralogy, providing validation for the method. Calcite and pyrite concentrations allowed advanced acid-base accounting for each mineral association, identifying 3 potential acid-producing associations and one potential acid-neutralizing association. The results target areas, where detailed hydrologic and kinetic tests would be valuable in the next stage of pit lake evaluation. Detailed understanding of wall rock mineralogy will help strengthen predictions of pit lake water quality

A mineral quantification method for wall rocks at open pit mines, and application to the Martha Au-Ag mine, Waihi, New Zealand

Energy Technology Data Exchange (ETDEWEB)

Castendyk, Devin N. [Environmental Science, SGES, University of Auckland, Tamaki Campus, Private Bag 92019, Auckland (New Zealand)]. E-mail: d.castendyk@auckland.ac.nz; Mauk, Jeffrey L. [Geology Department, University of Auckland, Private Bag 92019, Auckland (New Zealand); Webster, Jenny G. [Environmental Science, SGES, University of Auckland, Tamaki Campus, Private Bag 92019, Auckland (New Zealand)

2005-01-01

Pit lakes that result from open pit mining are potential water resources or potential environmental problems, depending on lake water quality. Wall rock mineralogy can affect lake chemistry if surface water inputs and/or groundwater inputs and/or lake water in contact with submerged wall rocks react with the wall rock minerals. This study presents a mineral quantification method to measure the distribution and concentration of wall rock minerals in open pit mines, and applies the method to the Martha epithermal Au-Ag mine, Waihi, New Zealand. Heterogeneous ore deposits, like Martha, require a large number of wall rock samples to accurately define mineral distributions. X-ray diffraction analyses of 125 wall rock samples identified the most abundant minerals in the wall rocks as quartz, adularia, albite, illite, chlorite, kaolinite, pyrite and calcite. Distribution maps of these minerals defined 8 relatively homogenous areas of wall rock referred to as 'mineral associations': weakly-altered, propylitic, fresh-argillic, weathered-argillic, oxidized, potassic, quartz veins, and post-mineralization deposits. X-ray fluorescence, Leco furnace, and neutron activation analyses of 46 representative samples produced the geochemical dataset used to assign quantities of elements to observed minerals, and to calculate average mineral concentrations in each association. Thin-section petrography and calcite concentrations from Sobek acid-digestions confirm the calculated mineralogy, providing validation for the method. Calcite and pyrite concentrations allowed advanced acid-base accounting for each mineral association, identifying 3 potential acid-producing associations and one potential acid-neutralizing association. The results target areas, where detailed hydrologic and kinetic tests would be valuable in the next stage of pit lake evaluation. Detailed understanding of wall rock mineralogy will help strengthen predictions of pit lake water quality.

Evidence for de-sulfidation to form native electrum in the Fire Creek epithermal gold-silver deposit, north-central Nevada

Science.gov (United States)

Perez, J.; Day, J. M.; Cook, G. W.

2012-12-01

The Fire Creek property is a newly developed and previously unstudied epithermal Au-Ag deposit located in the Northern Shoshone range of north central Nevada. The mineralization occurs within and above en echelon N-NW trending basaltic dykes that are hosted within a co-genetic and bimodal suite of mid-Miocene basalts and andesites formed in association with the Yellowstone hotspot-track. Previous studies of Au-Ag mineralization in the Great Basin have focused primarily on extensively mined and/or low-grade deposits. Therefore, the ability for unrestricted sampling of a major Au-Ag deposit early in its exploration and development represents an opportunity for refined understanding of epithermal ore genesis processes. New petrology reveals at least two distinct pulses of mineralization that in relative order of timing are: 1) S-rich veins which are associated with initial host-rock alteration; 2) quartz- and/or calcite-rich veins which vary from fine-grained to lath-like quartz crystals with large calcite crystals in vein centers. Native electrum occurs only within the second phase of mineralization and typically occurs within quartz and adjacent to cross-cut first-phase S-rich veins. In places the electrum appears to replace or form overgrowths around existing sulfide phases. High levels of gold and silver are found in both the first (0.8 g Au/tonne) and second-phase pulses (37 g Au/tonne). Fire Creek shares many similarities with its northern neighbor, the Mule Canyon Au-Ag deposit, with high Fe sulfide contents for some of the ores, altered wall-rocks and the presence of narrow and discontinuous gold-bearing siliceous veins. Like Fire Creek, Mule Canyon possesses two distinct mineralizing phases, a sulfide rich and a late stage calcite/silica assemblage. The first pulse appears to be identical in both locations with a variation of disseminated to euhedral iron-sulfides and associated intense alteration of host rock. However, Fire Creek differs from Mule Canyon in

A case study for the integration of predictive mineral potential maps

Science.gov (United States)

Lee, Saro; Oh, Hyun-Joo; Heo, Chul-Ho; Park, Inhye

2014-09-01

This study aims to elaborate on the mineral potential maps using various models and verify the accuracy for the epithermal gold (Au) — silver (Ag) deposits in a Geographic Information System (GIS) environment assuming that all deposits shared a common genesis. The maps of potential Au and Ag deposits were produced by geological data in Taebaeksan mineralized area, Korea. The methodological framework consists of three main steps: 1) identification of spatial relationships 2) quantification of such relationships and 3) combination of multiple quantified relationships. A spatial database containing 46 Au-Ag deposits was constructed using GIS. The spatial association between training deposits and 26 related factors were identified and quantified by probabilistic and statistical modelling. The mineral potential maps were generated by integrating all factors using the overlay method and recombined afterwards using the likelihood ratio model. They were verified by comparison with test mineral deposit locations. The verification revealed that the combined mineral potential map had the greatest accuracy (83.97%), whereas it was 72.24%, 65.85%, 72.23% and 71.02% for the likelihood ratio, weight of evidence, logistic regression and artificial neural network models, respectively. The mineral potential map can provide useful information for the mineral resource development.

Geology and mineralogy of the Au-As (Ag-Pb-Zn-Cu-Sb polymetallic deposit of Valiña-Azúmara (Lugo, NW Spain

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Martínez-Abad, I.

2015-12-01

Full Text Available Valiña-Azúmara is a polymetallic Au-As (Ag-Pb-Zn-Cu-Sb deposit, located in the province of Lugo (NW Spain, that was mined for arsenic at the beginning of the 20th century. The mineralization is hosted in a Variscan thrust fault with a dip direction of N247-261ºE, and N-S and NE-SW Late-Variscan faults. These structures are hosted in black slates, Cambrian in age. To a lesser extent, the mineralization also occurs disseminated within narrow, weakly silicified and sericited selvages. Mineralization is divided into two hypogene stages. The first consists of quartz, calcite, rutile, sericite, arsenopyrite and pyrite. Two types of pyrite (Py-I and Py-II are defined according to their chemical and textural characteristics. Py-II occurs as overgrowth of previous Py-I crystals. Py-II is As-rich (≤1.7 wt.% and often contains traces of Te, Zn, Cu, Bi, Sb and Au. The mineralized drill core sections show a significant correlation between Au and As. This is due to Au occurring as invisible Au within the Py-II grains, with contents of up to 176 ppm. The Au/As ratios of Py-II indicate that Au was deposited as Au1+, as solid solution within the pyrite structure. The second stage of mineralization is enriched in Ag-Pb-Zn-Cu-Sb, replacing the first stage, and consists of quartz, calcite, chlorite, sphalerite, jamesonite, Ag-rich tetrahedrite, freibergite, chalcopyrite, pyrrhotite and galena. Although jamesonite shows traces of Ag, the Cu-Ag sulfosalts are the main carriers of the Ag mineralization in the deposit, with contents that vary from 13.7 to 23.9 wt.% of Ag. In the most superficial levels of the area, secondary Fe oxide and hydroxide, scorodite and anglesite developed due to the oxidation of the ore.Valiña-Azúmara es un yacimiento filoniano de Au-As (Ag-Pb-Zn-Cu-Sb situado en la provincia de Lugo (NO España, que fue explotado por arsénico a principios del siglo XX. La mineralización se encuentra encajada en un cabalgamiento Varisco de direcci

Geochemistry of the Patricia Zn-Pb-Ag Deposit (paguanta, NE Chile)

Science.gov (United States)

Chinchilla Benavides, D.; Merinero Palomares, R.; Piña García, R.; Ortega Menor, L.; Lunar Hernández, R.

2013-12-01

are consistent with bulk rock analyses of selected and mineralized samples were similar correlations have been obtained. Ag positive correlations indicate that the formation of Ag-bearing minerals is mainly associated with galena, arsenopyrite and sphalerite occurrence. Au positive correlations indicate that this element occurs in close relationship with Ag-bearing minerals, arsenopyrite and sphalerite. The weak correlation between Cu and Ag and Au indicate that the formation of chalcopyrite is not related with the main stages of Ag-Au mineralization. The main conclusion of this study is that geochemical analyses along drill cores that cut mineralization confirm that the occurrence of Ag and Au in the Paguanta deposit is associated with the formation of galena, arsenopyrite and sphalerite. This study also confirm previous conclusions suggesting that the Patricia Pb-Zn-Ag ore deposit probably represents an example of epithermal mineralization of intermediate sulfidation state, with periods of lower sulfidation state during sphalerite deposition.

Au, Ag and Au:Ag colloidal nanoparticles synthesized by pulsed laser ablation as SERS substrates

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M. Vinod

2014-12-01

Full Text Available Chemically pure colloidal suspensions of gold and silver nanoparticles were synthesized using pulsed laser ablation. The dependence of laser fluence on the surface plasmon characteristics of the nanoparticles was investigated. Au:Ag colloidal suspensions were prepared by mixing highly monodisperse Au and Ag nanocolloids. The plasmon band of these mixtures was found to be highly sensitive to Au:Ag concentration ratio and wavelength of the laser beam used in the ablation process. The Au:Ag mixture consists of almost spherical shaped nanostructures with a tendency to join with adjacent ones. The surface enhanced Raman scattering activity of the Au, Ag and Au:Ag colloidal suspensions was tested using crystal violet as probe molecules. Enhancement in Raman signal obtained with Au:Ag substrates was found to be promising and strongly depends on its plasmon characteristics.

Precipitation of Ag2Te in the thermoelectric material AgSbTe2

International Nuclear Information System (INIS)

Sugar, Joshua D.; Medlin, Douglas L.

2009-01-01

The microstructure of AgSbTe 2 , prepared by solidification, is investigated using electron microscopy. During solidification and thermal treatment, the material separates into a two-phase mixture of a rocksalt phase, which is Ag 22 Sb 28 Te 50 , and silver telluride, Ag 2 Te. Ag 2 Te formation results either from eutectic solidification (large lamellar structures), or by solid-state precipitation (fine-scale particles). The crystal structure of the AgSbTe 2 phase determined by electron diffraction is consistent with a rocksalt structure that has a disordered cation sublattice. A preferred crystallographic orientation relationship at the interface between the matrix and the low-temperature monoclinic Ag 2 Te phase is defined and discussed. This orientation relationship is observed for both second-phase morphologies. In both cases, the orientation relationship originates from a topotactic (cube-on-cube) alignment of the Te sublattices in the initially cubic Ag 2 Te and the matrix at elevated temperature. This Te sublattice alignment is retained as the Ag 2 Te undergoes a cubic-to-monoclinic transformation during cooling. This orientation relationship is observed for both second-phase morphologies.

The Shah-Ali-Beiglou Zn-Pb-Cu (-Ag Deposit, Iran: An Example of Intermediate Sulfidation Epithermal Type Mineralization

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Khadijeh Mikaeili

2018-04-01

Full Text Available The Shah-Ali-Beiglou epithermal base metal-silver deposit is located in the Tarom-Hashjin metallogenic province (THMP in northwestern Iran. This deposit is hosted by quartz monzonite dikes of Oligocene age and surrounded by andesite to trachyandesite volcanic and volcaniclastic rocks of Eocene age. The subvolcanic rocks in the study area vary in composition from quartz-monzonite to monzonite and have metaluminous, calc-alkaline to shoshonitic affinity. These rocks have I-type geochemical characteristic and are related to post-collisional tectonic setting. The mineralization occurs as NE-SW and E-W-trending brecciated veins controlled by strike-slip and normal faults, which are associated to the Late Oligocene compressional regime. The mineral paragenesis of the vein mineralization is subdivided into pre-ore stage, ore stage, post-ore stage, and supergene stage. Pre-ore stage is dominated by quartz, sericite, and subhedral to anhedral pyrite as disseminated form. Ore-stage is represented by quartz, sphalerite (from 0.1 mol % to 4 mol % FeS, galena, chalcopyrite, tetrahedrite-tennantite, minor seligmannite and enargite, as vein-veinlet, cement and clast breccias. Post-ore stage is defined by deposition of quartz and carbonate along with minor barite, and supergene stage is characterized by bornite, chalcocite, covellite, hematite, goethite, and jarosite. The ore mineralization is associated with the silicic alteration. The styles of alteration are silicic, carbonate, sericitic, chloritic, and propylitic. Fluid inclusions in sphalerite have a wide range of salinities between 0.35 wt % and 21.4 wt % NaCl equivalent and homogenization temperatures range from 123 to 320 °C. The isotopic values of sulfides vary from 2.8‰ to 6.7‰ suggesting a magmatic source for the sulfur. In the present study, based on geological setting, alteration style of the host and wall rocks, main textures, mineral assemblages, composition of ore minerals, and structural

Oxygen isotope zonation at the Golden Cross low-sulfidation epithermal gold deposit, New Zealand

International Nuclear Information System (INIS)

Mauk, J.L.; Simpson, M.P.

2001-01-01

Forty-one whole rock samples from the Gold Cross low-sulfidation epithermal Au-Ag deposit have δ 18 O values that range from 4.4 to 9.3 per mil, with an average value of 7.0 per mil. Unaltered and weakly altered rocks have δ 18 O values greater than 8 per mil, and the orebody is surrounded by samples that are depleted in 18 O. A strongly silicified sample adjacent to the Empire Vein System has a δ 18 O value of 9.0 per mil, similar to previously reported analyses of vein quartz (7.0 to 11.7 per mil, average 9.4 per mil). This suggests that, in detail, Golden Cross may have a zone of 18 O-enriched wall rocks in the core of the deposit, adjacent to the main underground veins. Although some workers have suggested that stable isotope geochemistry may provide useful information for epithermal mineral deposit exploration, at Golden Cross this is not the case. Alteration minerals, major elements and trace elements all define larger, less ambiguous halos than the zone of 18 O-depleted wall rocks. (author). 21 refs., 3 figs., 1 tab

Precipitation of Ag{sub 2}Te in the thermoelectric material AgSbTe{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Sugar, Joshua D. [Materials Physics Department, Sandia National Laboratories, Livermore, CA (United States)], E-mail: jdsugar@sandia.gov; Medlin, Douglas L. [Materials Physics Department, Sandia National Laboratories, Livermore, CA (United States)

2009-06-10

The microstructure of AgSbTe{sub 2}, prepared by solidification, is investigated using electron microscopy. During solidification and thermal treatment, the material separates into a two-phase mixture of a rocksalt phase, which is Ag{sub 22}Sb{sub 28}Te{sub 50}, and silver telluride, Ag{sub 2}Te. Ag{sub 2}Te formation results either from eutectic solidification (large lamellar structures), or by solid-state precipitation (fine-scale particles). The crystal structure of the AgSbTe{sub 2} phase determined by electron diffraction is consistent with a rocksalt structure that has a disordered cation sublattice. A preferred crystallographic orientation relationship at the interface between the matrix and the low-temperature monoclinic Ag{sub 2}Te phase is defined and discussed. This orientation relationship is observed for both second-phase morphologies. In both cases, the orientation relationship originates from a topotactic (cube-on-cube) alignment of the Te sublattices in the initially cubic Ag{sub 2}Te and the matrix at elevated temperature. This Te sublattice alignment is retained as the Ag{sub 2}Te undergoes a cubic-to-monoclinic transformation during cooling. This orientation relationship is observed for both second-phase morphologies.

Ore deposits and epithermal evidences associated with intra-magmatic faults at Aïn El Araâr-Oued Belif ring structure (NW of Tunisia)

Science.gov (United States)

Aissa, Wiem Ben; Aissa, Lassaâd Ben; Amara, Abdesslem Ben Haj; Tlig, Said; Alouani, Rabah

2017-03-01

Hydrothermal ore deposits at Aïn El Araâr-Oued Belif location are classified as epithermal deposits type. The ore bodies are hosted by upper Turonian (8-9 M.y) volcanic rhyodacitic complex. Polymetallic sulfide orebodies are mainly concentrated within intra-magmatic faults. Petrographic, XRD, and TEM-STEM investigations revealed that ore minerals are essentially, arsenopyrite, pyrite, chalcopyrite, pyrrhotite, hematite, goethite and magnetite with Au, Ag and Pt trace metals. Gangue minerals are mainly adularia, quartz, sericite, alunite, tridymite, chlorite, phlogopite and smectite. Epithermal alteration is well zoned with four successive characteristic zones: (1) zone of quartz-adularia-sericite and rare alunite; (2) zone of kaolinite and plagioclase albitization; (3) intermediate zone of illite-sericite; (4) sapropelic alteration type zone of chlorite-smectite and rare illite. This can be interpreted as a telescoping of two different acidity epithermal phases; low sulfidation (adularia-sericite) and high sulfidation (quartz-alunite), separated in time or due to a gradual increase of fluids acidity and oxicity within the same mineralization phase. Brecciated macroscopic facies with fragments hosting quartz-adularia-sericite minerals (low-sulfidation phase) without alunite, support the last hypothesis. Geodynamic context and mineral alteration patterns are closely similar to those of Maria Josefa gold mine at SE of Spain which exhibit a volcanic-hosted epithermal ore deposit in a similar vein system, within rhyolitic ignimbrites, altered to an argillic assemblage (illite-sericite abundant and subordinate kaolinite) that grades outwards into propylitic alteration (Sanger-von Oepen et al. (1990)). Mineralogical and lithologic study undertaken in the volcanic host rock at Aïn El Araâr-Oued Belif reveals a typical epithermal low-sulfidation and high-sulfidation ore deposits with dominance of low-sulfidation. Host rocks in these systems range from silicic to

Geochemical evaluation of mining wastes (tailings or tails) of epithermal ore mineralization, Hidalgo, Mexico

International Nuclear Information System (INIS)

Moreno, Raul; Monroy, Marcos G.; Castaneda, E. Pedro

2009-01-01

The mining district Pachuca-Real del Monte is located to the center-east of Mexico, between the geographical coordinates 20 degrees celsius 07 minutes 30 seconds north latitude and 98 degrees celsius 44 minutes 00 seconds of length west. The residues are derived from an epithermal mineralization. Concentrations of Pb and the Mn are significant. The mineralization is consisted of pyrite, limonite-goethite-hematite, sphalerite, galena, and chalcopyrite associated with quartz, calcite and silicates. X-rays diffraction patterns have determined quartz as the mayor mineral phase, with minor gypsum, calcite, alunite, and pyrite. The statistical analysis has presented the frequent association of Zn-Cd. The microanalysis with the scanning electronic microscope and electronic microprobe have showed the neoformation of the pyrite and the oxidation and precipitate of sulfides. The tests NOM-053 and EPA-1312 have showed that the Cd, Ni, Ag, Pb Mn, Zn, and As do not exceed the LMP. Only the Pb has been superior to the LMP in the first test. These residues might be classified as dangerous with regard to the Pb. (author) [es

Identification of Ag-acceptors in $^{111}Ag^{111}Cd$ doped ZnTe and CdTe

CERN Document Server

Hamann, J; Deicher, M; Filz, T; Lany, S; Ostheimer, V; Strasser, F; Wolf, H; Wichert, T

2000-01-01

Nominally undoped ZnTe and CdTe crystals were implanted with radioactive /sup 111/Ag, which decays to /sup 111/Cd, and investigated by photoluminescence spectroscopy (PL). In ZnTe, the PL lines caused by an acceptor level at 121 meV are observed: the principal bound exciton (PBE) line, the donor-acceptor pair (DAP) band, and the two-hole transition lines. In CdTe, the PBE line and the DAP band that correspond to an acceptor level at 108 meV appear. Since the intensities of all these PL lines decrease in good agreement with the half-life of /sup 111/Ag of 178.8 h, both acceptor levels are concluded to be associated with defects containing a single Ag atom. Therefore, the earlier assignments to substitutional Ag on Zn- and Cd-lattice sites in the respective II-VI semiconductors are confirmed. The assignments in the literature of the S/sub 1/, S /sub 2/, and S/sub 3/ lines in ZnTe and the X/sub 1//sup Ag/, X/sub 2 //sup Ag//C/sub 1//sup Ag/, and C/sub 2//sup Ag/ lines in CdTe to Ag- related defect complexes are ...

Mineralized breccia clasts: a window into hidden porphyry-type mineralization underlying the epithermal polymetallic deposit of Cerro de Pasco (Peru)

Science.gov (United States)

Rottier, Bertrand; Kouzmanov, Kalin; Casanova, Vincent; Bouvier, Anne-Sophie; Baumgartner, Lukas P.; Wälle, Markus; Fontboté, Lluís

2018-01-01

Cerro de Pasco (Peru) is known for its large epithermal polymetallic (Zn-Pb-Ag-Cu-Bi) mineralization emplaced at shallow level, a few hundred meters below the paleo-surface, at the border of a large diatreme-dome complex. Porphyry-style veins crosscutting hornfels and magmatic rock clasts are found in the diatreme breccia and in quartz-monzonite porphyry dikes. Such mineralized veins in clasts allow investigation of high-temperature porphyry-style mineralization developed in the deep portions of magmatic-hydrothermal systems. Quartz in porphyry-style veins contains silicate melt inclusions as well as fluid and solid mineral inclusions. Two types of high-temperature (> 600 °C) quartz-molybdenite-(chalcopyrite)-(pyrite) veins are found in the clasts. Early, thin (1-2 mm), and sinuous HT1 veins are crosscut by slightly thicker (up to 2 cm) and more regular HT2 veins. The HT1 vein quartz hosts CO2- and sulfur-rich high-density vapor inclusions. Two subtypes of the HT1 veins have been defined, based on the nature of mineral inclusions hosted in quartz: (i) HT1bt veins with inclusions of K-feldspar, biotite, rutile, and minor titanite and (ii) HT1px veins with inclusions of actinolite, augite, titanite, apatite, and minor rutile. Using an emplacement depth of the veins of between 2 and 3 km (500 to 800 bar), derived from the diatreme breccia architecture and the supposed erosion preceding the diatreme formation, multiple mineral thermobarometers are applied. The data indicate that HT1 veins were formed at temperatures > 700 °C. HT2 veins host assemblages of polyphase brine inclusions, generally coexisting with low-density vapor-rich inclusions, trapped at temperatures around 600 °C. Rhyolitic silicate melt inclusions found in both HT1 and HT2 veins represent melt droplets transported by the ascending hydrothermal fluids. LA-ICP-MS analyses reveal a chemical evolution coherent with the crystallization of an evolved rhyolitic melt. Quartz from both HT1 and HT2 veins

The magmatic model for the origin of Archean Au-quartz vein ore systems: an assessment of the evidence

International Nuclear Information System (INIS)

Spooner, E.T.C.

1991-01-01

The magmatic model for the origin of Archean Au-quartz vein ore systems suggests that Au was derived by partition between silicate (± sulphide) melts of certain compositions and H 2 O-CO 2 -NaCl magmatic fluids. Supporting evidence includes partial/structural geological relationships, timing relationships, H and C isotope geochemistry, probable primary Au enrichment in the Lamaque stocks, and fluid inclusion volatile geochemistry. Evidence is currently negative with respect to various within- and sub-greenstone belt metamorphic/deep crustal fluid models for primary Au mineralization; however a U-Pb age for vein stage 3 sphene from the Camflo deposit, Quebec which is ∼ 55-60 Ma younger than the host stock at 2685-2680 Ma indicates dissolution/reprecipitation of Au by late, (?) upper crustal saline fluids. Evidence is accumulating that epithermal-meso thermal Au-Ag mineralization in island arc and cordilleran settings may also have been magmatically derived ± high level fluid mixing from calc-alkaline, shoshonitic and other igneous compositions. (author)

Age and tectonomagmatic setting of the Eocene Çöpler-Kabataş magmatic complex and porphyry-epithermal Au deposit, East Central Anatolia, Turkey

Science.gov (United States)

İmer, Ali; Richards, Jeremy P.; Creaser, Robert A.

2013-06-01

The Çöpler epithermal Au deposit and related subeconomic porphyry Cu-Au deposit is hosted by the middle Eocene Çöpler-Kabataş magmatic complex in central eastern Anatolia. The intrusive rocks of the complex were emplaced into Late Paleozoic-Mesozoic metamorphosed sedimentary basement rocks near the northeastern margin of the Tauride-Anatolide Block. Igneous biotite from two samples of the magmatic complex yielded 40Ar/39Ar plateau ages of 43.75 ± 0.26 Ma and 44.19 ± 0.23, whereas igneous hornblende from a third sample yielded a plateau age of 44.13 ± 0.38. These ages closely overlap with 40Ar/39Ar ages of hydrothermal sericite (44.44 ± 0.28 Ma) and biotite (43.84 ± 0.26 Ma), and Re-Os ages from two molybdenite samples (44.6 ± 0.2 and 43.9 ± 0.2 Ma) suggesting a short-lived (history at Çöpler. No suitable minerals were found that could be used to date the epithermal system, but it is inferred to be close in age to the precursor porphyry system. The Çöpler-Kabataş intrusive rocks show I-type calc-alkaline affinities. Their normalized trace element patterns show enrichments in large ion lithophile and light rare earth elements and relative depletions in middle and heavy rare earth elements, resembling magmas generated in convergent margins. However, given its distance from the coeval Eocene Maden-Helete volcanic arc, the complex is interpreted to be formed in a back-arc setting, in response to Paleocene slab roll-back and upper-plate extension. The tectonomagmatic environment of porphyry-epithermal mineralization at Çöpler is comparable to some other isolated back-arc porphyry systems such as Bajo de la Alumbrera (Argentina) or Bingham Canyon (USA).

Diagnostic Genesis Features of Au-Ag Selenide-Telluride Mineralization of Western Java Deposits

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Euis Tintin Yuningsih

2016-01-01

Full Text Available DOI: 10.17014/ijog.3.1.67-76The ore mineralogy of the westernmost part of West Java such as Pongkor, Cibaliung, Cikidang, Cikotok, and Cirotan are characterized by the dominance of silver-arsenic-antimony sulfosalt with silver selenides and rarely tellurides over the argentite, whereas the eastern part of West Java including Arinem and Cineam deposits are dominated by silver-gold tellurides. Mineralogy of Se-type deposits at Pongkor, Cikidang, Cibaliung, Cisungsang, and Cirotan and Te-type deposits at Arinem and Cineam shows their different geochemical characteristics. Mineralogical and geochemical differences can be explained by variation of physico-chemical conditions that existed during gold-silver deposition by applying the phase relation among sulfide, telluride, and selenide mineral association in the deposits. The relative values of ƒSe2(g, ƒTe(g, and ƒS2(g control the actual presence of selenide or telluride minerals within the West Java deposits, which also depend on their concentrations in the hydrothermal fluid. Even though the concentration of selenium in the hydrothermal fluid of Te-type deposits might have been similar or even higher than that in the Se-type, early substitution of selenium in the sulfide minerals prevents its concentration in the hydrothermal fluid to the levels for precipitating selenide minerals. Therefore, early sulfide mineral deposition from reduction fluids will not increase the ƒSe2(g/ƒS2(g ratio to form selenide minerals in Te-type deposits of Arinem and Cineam, other than selenium-bearing sulfide mineral such as Se-bearing galena or Se-bearing pyrargyrite-proustite.

Application of enzyme leach soil analysis for epithermal gold exploration in the Andes of Ecuador

Energy Technology Data Exchange (ETDEWEB)

Williams, T.M.; Gunn, A.G. [British Geological Survey, Nottingham (United Kingdom)

2002-07-01

Enzyme Leach (EL) soil surveys were undertaken over known epithermal Au mineralisation at El Mozo and Llano Largo, Azuay, Ecuador to assess the utility of the technique for identifying such deposits in the Ecuadorian Andes. The results indicate the development of both apical- and oxidation-type EL anomalies over auriferous structures at the two sites, the former systematically incorporating Au, and the latter Cl and Br. The spectrum of elements responsive to mineralisation at El Mozo (Cl, Br, I, La, Ce, Nd, Cu, Pb, Au, As, Sb, Ag, Zr, Sr) was found to be considerably greater than at Llano Largo (Cl, Br, Au, As, Sb, Ag, Zn), probably reflecting the contrasting high- and low-sulphidation assemblages of the two prospects. Ratios of EL versus aqua-regia extractable trace element concentrations ranged from 1: < 100 for Mn to 1: >400 for chalcophile elements such as Pb, Sb, As, Bi and Ag. Strong correlations between the concentrations of several analytes (including Mn, Sr, Cu, Co, As) extracted by the two procedures indicate, however, that EL datasets are extensively influenced by bulk matrix composition. Spatial variations of EL extractable Mn were found to exert no major influence on apical or oxidation suite anomaly patterns at El Mozo. However, Mn-normalisation of halogen data for Llano Largo elucidated otherwise obscure oxidation features, potentially related to Au mineralisation. Ratios between elements subject to apical enrichment and those of the oxidation suite (e.g. Cl/Au and Bi/Br) were found to highlight known Au targets with improved clarity. The formation mechanism of the recorded Au anomalies is uncertain, but may involve physical enrichment of Au in the soil during pedogenesis with subsequent in-situ formation of (EL soluble) Au halide complexes. The strength of such apical features is, in part, probably a function of the minimal depths to mineralisation which characterise El Mozo and Llano Largo. Oxidation halos formed by volatile non-metallic elements

The extraction characteristic of Au-Ag from Au concentrate by thiourea solution

Science.gov (United States)

Kim, Bongju; Cho, Kanghee; On, Hyunsung; Choi, Nagchoul; Park, Cheonyoung

2013-04-01

The cyanidation process has been used commercially for the past 100 years, there are ores that are not amenable to treatment by cyanide. Interest in alternative lixiviants, such as thiourea, halogens, thiosulfate and malononitrile, has been revived as a result of a major increase in gold price, which has stimulated new developments in extraction technology, combined with environmental concern. The Au extraction process using the thiourea solvent has many advantages over the cyanidation process, including higher leaching rates, faster extraction time and less than toxicity. The purpose of this study was investigated to the extraction characteristic of Au-Ag from two different Au concentrate (sulfuric acid washing and roasting) under various experiment conditions (thiourea concentration, pH of solvent, temperature) by thiourea solvent. The result of extraction experiment showed that the Au-Ag extraction was a fast extraction process, reaching equilibrium (maximum extraction rate) within 30 min. The Au-Ag extraction rate was higher in the roasted concentrate than in the sulfuric acid washing. The higher the Au-Ag extraction rate (Au - 70.87%, Ag - 98.12%) from roasted concentrate was found when the more concentration of thiourea increased, pH decreased and extraction temperature increased. This study informs extraction method basic knowledge when thiourea was a possibility to eco-/economic resources of Au-Ag utilization studies including the hydrometallurgy.

Study on antibacterial activity of chemically synthesized PANI-Ag-Au nanocomposite

Energy Technology Data Exchange (ETDEWEB)

Boomi, Pandi [Department of Industrial Chemistry, School of Chemical Sciences, Alagappa University, Karaikudi 630 003, Tamil Nadu (India); Prabu, Halliah Gurumallesh, E-mail: hgprabu2010@gmail.com [Department of Industrial Chemistry, School of Chemical Sciences, Alagappa University, Karaikudi 630 003, Tamil Nadu (India); Manisankar, Paramasivam [Department of Industrial Chemistry, School of Chemical Sciences, Alagappa University, Karaikudi 630 003, Tamil Nadu (India); Ravikumar, Sundaram [Department of Oceanography and Coastal Area Studies, School of Marine Sciences, Alagappa University, Thondi Campus 623 409, Tamil Nadu (India)

2014-05-01

Graphical abstract: - Highlights: • New method of synthesizing PANI-Ag-Au nanocomposite. • Surface Plasmon resonance and formation of composite at nano level were analyzed. • HR-TEM study revealed uniform distribution of nanoparticles. • PANI-Ag-Au nanocomposite exhibited good antibacterial activity. - Abstract: Pristine polyaniline (PANI), PANI-Ag, PANI-Au and PANI-Ag-Au nanocomposites have been successfully synthesized by chemical oxidative polymerization method using aniline as monomer, ammonium persulphate as oxidant and metal (Ag, Au and Ag-Au) colloids. UV-Vis analysis exhibited surface Plasmon resonances of Ag, Au, Ag-Au nanoparticles. FT-IR spectra revealed the shift in peak position of N-H stretching. X-ray diffraction (XRD) results confirm the presence of Ag, Au and Au-Ag nanoparticles. HR-TEM images show nanosizes of Ag, Au, Ag-Au and the incorporation of such nanoparticles into the PANI matrix. Pristine PANI, PANI-Ag, PANI-Au and PANI-Ag-Au nanocomposites were tested for antibacterial activity by agar well diffusion method. PANI-Ag-Au nanocomposite exhibited higher antibacterial activity against both gram-positive [Streptococcus sp. (MTCC 890), Staphylococcus sp. (MTCC 96)] and gram-negative bacteria [Escherichia coli (MTCC 1671) and Klebsiella sp. (MTCC 7407)] when compared with PANI-Ag nanocomposite, PANI-Au nanocomposite and pristine PANI. The novelty of this study is the polymer-bimetal synthesis and its antibacterial potential.

Geology mineralogy, structure and texture of Agh-Otagh base- precious metal mineralization (North Takab

Directory of Open Access Journals (Sweden)

Nahid Rahmati

2017-07-01

Full Text Available The Agh-Otagh mineralization area in the north of Takab, was formed within the andesistic tuffaceous rocks of the Oligo- Miocene age. Mineralization include polymetallic (Cu-Pb-Zn-Au-Ag quartz veins and silicified zones, which occurred as breccia and vein- veinlets with comb, cockade and disseminated textures. Chalcopyrite, pyrite, galena and sphalerite are common ore minerals. Alteration zones consist of silicification, sericitization, argillitic, propelitic and carbonatization. Cu-Au mineralization is associated with silicification and sericitization. Analytical results of the samples from the ore- bearing quartz veins and the silicified zones indicate that the highest grade for Au is 664 ppb (ave.181 ppb. The highest and the average grades for Ag, Cu, Pb, and Zn are 120 ppm (300 ppm, 1.3 % (0.38 %, 5.5 % (0.06 % and 4.5 % (0.28 %, respectively. The investigations indicate that the Agh-Otagh mineralization was formed in four stages. In the first stage or the pre-mineralization stage, the host rock, as a result of hydrothermal process, underwent brecciation and some quartz veins and siliceous cap were formed. In the second stage or the mineralization stage the sulfide minerals formed within the quartz veins and silicification zones developed at the third stage, some unmineralized quartz, barite and carbonate vein- veinlets crosscut the previous stages. The last stage of mineralization related to supergene processes. Based on geological, mineralogical, alteration, structural and textural evidences, the Agh-Otagh base- precious metal mineralization is similar to the medium sulfidation epithermal deposits.

Controlled Synthesis of Au@AgAu Yolk-Shell Cuboctahedra with Well-Defined Facets.

Science.gov (United States)

Londono-Calderon, Alejandra; Bahena, Daniel; Yacaman, Miguel J

2016-08-02

The synthesis of Au@AgAu yolk-shell cuboctahedra nanoparticles formed by galvanic replacement in a seed-mediated method is described. Initially, single-crystal Au seeds are used for the formation of Au@Ag core-shell nanocubes, which serve as the template material for the deposition of an external Au layer. The well-controlled synthesis yields the formation of cuboctahedra nanoparticles with smooth inner and outer Au/Ag surfaces. The deposition/oxidation process is described to understand the formation of cuboctahedra and octahedra nanoparticles. The Au core maintains the initial morphology of the seed and remains static at the center of the yolk-shell because of residual Ag. Structural analysis of the shell indicates intrinsic stacking faults (SFs) near the surface. Energy dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS) compositional analysis show an Au-Ag nonordered alloy forming the shell. The three-dimensional structure of the nanoparticles presented open facets on the [111] as observed by electron tomography SIRT reconstruction over a stack of high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) images. The geometrical model was validated by analyzing the direction of streaks in coherent nanobeam diffraction (NBD). The catalytic activity was evaluated using a model reaction based on the reduction of 4-nitrophenol (4-NTP) by NaBH4 in the presence of Au@AgAu yolk-shell nanoparticles.

Geochemical and modal data for igneous rocks associated with epithermal mineral deposits

Science.gov (United States)

du Bray, Edward A.

2014-01-01

The purposes of this report are to (1) present available geochemical and modal data for igneous rocks associated with epithermal mineral deposits and (2) to make those data widely and readily available for subsequent, more in-depth consideration and interpretation. Epithermal precious and base-metal deposits are commonly associated with subduction-related calc-alkaline to alkaline arc magmatism as well as back-arc continental rift magmatism. These deposits form in association with compositionally diverse extrusive and intrusive igneous rocks. Temperature and depth regimes prevailing during deposit formation are highly variable. The deposits form from hydrothermal fluids that range from acidic to near-neutral pH, and they occur in a variety of structural settings. The disparate temperature, pressure, fluid chemistry, and structural controls have resulted in deposits with wide ranging characteristics. Economic geologists have employed these characteristics to develop classification schemes for epithermal deposits and to constrain the important genetic processes responsible for their formation.

Structural and electric properties of AgGaTe{sub 2} layers prepared using mixed source of Ag{sub 2}Te and Ga{sub 2}Te{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Uruno, Aya [Department of Electrical Engineering and Bioscience, Waseda University, Tokyo (Japan); Kobayashi, Masakazu [Department of Electrical Engineering and Bioscience, Waseda University, Tokyo (Japan); Kagami Memorial Research Institute for Materials Science and Technology, Waseda University, Tokyo (Japan)

2017-01-15

AgGaTe{sub 2} layers were prepared on Si substrates by a closed space sublimation method using a mixed powder source of Ag{sub 2}Te and Ga{sub 2}Te{sub 3}. Ag{sub 2}Te buffer layer deposition was introduced to eliminate melt-back etching. The effect of the molar ratio of Ag{sub 2}Te and Ga{sub 2}Te{sub 3} in the mixed source on the crystallinity of the AgGaTe{sub 2} layer was investigated. The composition and the phase of the layer was found to change depending on the molar ratio in the deposits, which could be controlled by the source molar ratio along with the Ag{sub 2}Te buffer layer thickness. It was confirmed that (112) oriented uniform AgGaTe{sub 2} layer with an abrupt interface between AgGaTe{sub 2} and Si was formed after those parameters were tuned. The obtained layer exhibited the acceptor concentration of around 2.5 x 10{sup 16} cm{sup -3}. A solar cell was fabricated using the p-AgGaTe{sub 2}/n-Si heterojunction, and exhibited a conversion efficiency of 1.15%. (copyright 2016 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Transformation of Ag nanocubes into Ag-Au hollow nanostructures with enriched Ag contents to improve SERS activity and chemical stability.

Science.gov (United States)

Yang, Yin; Zhang, Qiang; Fu, Zheng-Wen; Qin, Dong

2014-03-12

We report a strategy to complement the galvanic replacement reaction between Ag nanocubes and HAuCl4 with co-reduction by ascorbic acid (AA) for the formation of Ag-Au hollow nanostructures with greatly enhanced SERS activity. Specifically, in the early stage of synthesis, the Ag nanocubes are sharpened at corners and edges because of the selective deposition of Au and Ag atoms at these sites. In the following steps, the pure Ag in the nanocubes is constantly converted into Ag(+) ions to generate voids owing to the galvanic reaction with HAuCl4, but these released Ag(+) ions are immediately reduced back to Ag atoms and are co-deposited with Au atoms onto the nanocube templates. We observe distinctive SERS properties for the Ag-Au hollow nanostructures at visible and near-infrared excitation wavelengths. When plasmon damping is eliminated by using an excitation wavelength of 785 nm, the SERS activity of the Ag-Au hollow nanostructures is 15- and 33-fold stronger than those of the original Ag nanocubes and the Ag-Au nanocages prepared by galvanic replacement without co-reduction, respectively. Additionally, Ag-Au hollow nanostructures embrace considerably improved stability in an oxidizing environment such as aqueous H2O2 solution. Collectively, our work suggests that the Ag-Au hollow nanostructures will find applications in SERS detection and imaging.

Fabricating a Homogeneously Alloyed AuAg Shell on Au Nanorods to Achieve Strong, Stable, and Tunable Surface Plasmon Resonances

KAUST Repository

Huang, Jianfeng

2015-08-13

Colloidal metal nanocrystals with strong, stable, and tunable localized surface plasmon resonances (SPRs) can be useful in a corrosive environment for many applications including field-enhanced spectroscopies, plasmon-mediated catalysis, etc. Here, a new synthetic strategy is reported that enables the epitaxial growth of a homogeneously alloyed AuAg shell on Au nanorod seeds, circumventing the phase segregation of Au and Ag encountered in conventional synthesis. The resulting core–shell structured bimetallic nanorods (AuNR@AuAg) have well-mixed Au and Ag atoms in their shell without discernible domains. This degree of mixing allows AuNR@AuAg to combine the high stability of Au with the superior plasmonic activity of Ag, thus outperforming seemingly similar nanostructures with monometallic shells (e.g., Ag-coated Au NRs (AuNR@Ag) and Au-coated Au NRs (AuNR@Au)). AuNR@AuAg is comparable to AuNR@Ag in plasmonic activity, but that it is markedly more stable toward oxidative treatment. Specifically, AuNR@AuAg and AuNR@Ag exhibit similarly strong signals in surface-enhanced Raman spectroscopy that are some 30-fold higher than that of AuNR@Au. When incubated with a H2O2 solution (0.5 m), the plasmonic activity of AuNR@Ag immediately and severely decayed, whereas AuNR@AuAg retained its activity intact. Moreover, the longitudinal SPR frequency of AuNR@AuAg can be tuned throughout the red wavelengths (≈620–690 nm) by controlling the thickness of the AuAg alloy shell. The synthetic strategy is versatile to fabricate AuAg alloyed shells on different shaped Au, with prospects for new possibilities in the synthesis and application of plasmonic nanocrystals.

Syntheses and crystal structures of BaAgTbS{sub 3}, BaCuGdTe{sub 3}, BaCuTbTe{sub 3}, BaAgTbTe{sub 3}, and CsAgUTe{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Prakash, Jai; Beard, Jessica C.; Ibers, James A. [Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, IL 60208-3113 (United States); Mesbah, Adel [Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, IL 60208-3113 (United States); ICSM-UMR 5257 CNRS/CEA/UM2/ENSCM, Bat 426, BP 17171, 30207 Bagnols/Ceze (France)

2015-06-15

Five new quaternary chalcogenides of the 1113 family, namely BaAgTbS{sub 3}, BaCuGdTe{sub 3}, BaCuTbTe{sub 3}, BaAgTbTe{sub 3}, and CsAgUTe{sub 3}, were synthesized by the reactions of the elements at 1173-1273 K. For CsAgUTe{sub 3} CsCl flux was used. Their crystal structures were determined by single-crystal X-ray diffraction studies. The sulfide BaAgTbS{sub 3} crystallizes in the BaAgErS{sub 3} structure type in the monoclinic space group C{sup 3},{sub 2h}-C2/m, whereas the tellurides BaCuGdTe{sub 3}, BaCuTbTe{sub 3}, BaAgTbTe{sub 3}, and CsAgUTe{sub 3} crystallize in the KCuZrS{sub 3} structure type in the orthorhombic space group D{sup 1},{sub 2}{sup 7},{sub h}-Cmcm. The BaAgTbS{sub 3} structure consists of edge-sharing [TbS{sub 6}{sup 9-}] octahedra and [AgS{sub 5}{sup 9-}] trigonal pyramids. The connectivity of these polyhedra creates channels that are occupied by Ba atoms. The telluride structure features {sup 2}{sub ∞}[MLnTe{sub 3}{sup 2-}] layers for BaCuGdTe{sub 3}, BaCuTbTe{sub 3}, BaAgTbTe{sub 3}, and {sup 2}{sub ∞}[AgUTe{sub 3}{sup 1-}] layers for CsAgUTe{sub 3}. These layers comprise [MTe{sub 4}] tetrahedra and [LnTe{sub 6}] or [UTe{sub 6}] octahedra. Ba or Cs atoms separate these layers. As there are no short Q..Q (Q = S or Te) interactions these compounds achieve charge balance as Ba{sup 2+}M{sup +}Ln{sup 3+}(Q{sup 2-}){sub 3} (Q = S and Te) and Cs{sup +}Ag{sup +}U{sup 4+}(Te{sup 2-}){sub 3}. (Copyright copyright 2015 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Local structure of disordered Au-Cu and Au-Ag alloys

International Nuclear Information System (INIS)

Frenkel, A. I.; Machavariani, V. Sh.; Rubshtein, A.; Rosenberg, Yu.; Voronel, A.; Stern, E. A.

2000-01-01

X-ray-absorption fine structure (XAFS) and x-ray-diffraction (XRD) measurements of disordered alloys Au x Cu 1-x and Au 0.5 Ag 0.5 prepared by melt spinning were performed. In the Au 0.5 Ag 0.5 alloy, no significant local deviations of the atoms from the average fcc lattice were detected while in Au x Cu 1-x alloys, significant deviations of atoms from the average fcc lattice were found. Mean-square vibrations of the Cu-Cu distances revealed by the XAFS in Au x Cu 1-x alloys indicate the weakening of contact between Cu atoms in the dilute limit. Our computer simulation for Au x Cu 1-x clusters of 10 5 atoms reproduces the main features of both the XAFS and XRD data

Facile synthesis of Ag nanocubes and Au nanocages.

Science.gov (United States)

Skrabalak, Sara E; Au, Leslie; Li, Xingde; Xia, Younan

2007-01-01

This protocol describes a method for the synthesis of Ag nanocubes and their subsequent conversion into Au nanocages via the galvanic replacement reaction. The Ag nanocubes are prepared by a rapid (reaction time nanocubes. With this method, Ag nanocubes can be prepared and isolated for use within approximately 3 h. The Ag nanocubes can then serve as sacrificial templates for the preparation of Au nanocages, with a method for their preparation also described herein. The procedure for Au nanocage preparation and isolation requires approximately 5 h.

Multiple Mesozoic mineralization events in South China—an introduction to the thematic issue

Science.gov (United States)

Hu, Rui-Zhong; Zhou, Mei-Fu

2012-08-01

Mesozoic mineral deposits in South China include world-class deposits of W, Sn and Sb and those that provide the major sources of Ta, Cu, Hg, As, Tl, Pb, Zn, Au and Ag for the entire country. These deposits can be classified into polymetallic hydrothermal systems closely related to felsic intrusive rocks (Sn-W -Mo granites, Cu porphyries, polymetallic and Fe skarns, and polymetallic vein deposits) and low-temperature hydrothermal systems with no direct connection to igneous activities (MVT deposits, epithermal Au and Sb deposits). Recent studies have shown that they formed in the Triassic (Indosinian), Jurassic-Cretaceous (Early Yanshanian), and Cretaceous (Late Yanshanian) stages. Indosinian deposits include major MVT (Pb-Zn-Ag) deposits and granite-related W-Sn deposits. Early Yanshanian deposits are low-temperature Sb-Au and high-temperature W-Sn and Cu porphyry types. Many Late Yanshanian deposits are low-temperature Au-As-Sb-Hg and U deposits, and also include high-temperature W-Sn polymetallic deposits. The formation of these deposits is linked with a specific tectonothermal evolution and igneous activities. This special issue brings together some of the latest information in eight papers that deal with the origins and tectonic environments of mineral deposits formed in these stages. We anticipate that this issue will stimulate more interests in these ore deposits in South China.

A simple approach for facile synthesis of Ag, anisotropic Au and bimetallic (Ag/Au) nanoparticles using cruciferous vegetable extracts

Energy Technology Data Exchange (ETDEWEB)

Jacob, Jasmine; Mukherjee, Tulsi; Kapoor, Sudhir, E-mail: sudhirk@barc.gov.in

2012-10-01

We present a simple and straightforward approach for the synthesis and stabilization of relatively monodisperse Ag, Au and bimetallic (Ag/Au) nanoparticles by using cruciferous vegetable (green/red) extracts by simply adjusting the pH environment in the aqueous medium. The vegetable extracts act both as reducing and capping agents. The monometallic and bimetallic nanoparticles of Ag and Au so obtained were characterized by UV-visible spectroscopy, X-ray diffraction (XRD), dynamic light scattering (DLS) and transmission electron microscopy (TEM). It is shown that red cabbage extract can be used for the preparation of anisotropic Au nanoparticles. The formation of Au anisotropic nanoparticles was found to depend on a number of environmental factors, such as the pH of the reaction medium, reaction time, and initial reactant concentrations. Additionally, it is shown that these extract-stabilized Au and Ag nanoparticles can be used as a seed for preparation of bimetallic Au/Ag nanoparticles. For bimetallic alloy nanoparticles the absorption peak was observed between the two maxima of the corresponding metallic particles. The surface plasmon absorption maxima for bimetallic nanoparticles changed linearly with increasing Au mole ratio content in various alloy compositions. It has been shown that the formation of hollow Au spheres depends on the experimental conditions. - Graphical abstract: TEM image of gold nanoparticles at pH 3.27 formed by red cabbage extract. Highlights: Black-Right-Pointing-Pointer First report on the reactivity of the extracts toward metal ions using a spectrophotometric technique. Black-Right-Pointing-Pointer Red cabbage extract has better reducing properties than green cabbage extract. Black-Right-Pointing-Pointer Red cabbage extract can reduce metal ions at any pH. Black-Right-Pointing-Pointer Reduction of metal ions can have important consequences in the study of soil chemistry.

A simple approach for facile synthesis of Ag, anisotropic Au and bimetallic (Ag/Au) nanoparticles using cruciferous vegetable extracts

International Nuclear Information System (INIS)

Jacob, Jasmine; Mukherjee, Tulsi; Kapoor, Sudhir

2012-01-01

We present a simple and straightforward approach for the synthesis and stabilization of relatively monodisperse Ag, Au and bimetallic (Ag/Au) nanoparticles by using cruciferous vegetable (green/red) extracts by simply adjusting the pH environment in the aqueous medium. The vegetable extracts act both as reducing and capping agents. The monometallic and bimetallic nanoparticles of Ag and Au so obtained were characterized by UV–visible spectroscopy, X-ray diffraction (XRD), dynamic light scattering (DLS) and transmission electron microscopy (TEM). It is shown that red cabbage extract can be used for the preparation of anisotropic Au nanoparticles. The formation of Au anisotropic nanoparticles was found to depend on a number of environmental factors, such as the pH of the reaction medium, reaction time, and initial reactant concentrations. Additionally, it is shown that these extract-stabilized Au and Ag nanoparticles can be used as a seed for preparation of bimetallic Au/Ag nanoparticles. For bimetallic alloy nanoparticles the absorption peak was observed between the two maxima of the corresponding metallic particles. The surface plasmon absorption maxima for bimetallic nanoparticles changed linearly with increasing Au mole ratio content in various alloy compositions. It has been shown that the formation of hollow Au spheres depends on the experimental conditions. - Graphical abstract: TEM image of gold nanoparticles at pH 3.27 formed by red cabbage extract. Highlights: ► First report on the reactivity of the extracts toward metal ions using a spectrophotometric technique. ► Red cabbage extract has better reducing properties than green cabbage extract. ► Red cabbage extract can reduce metal ions at any pH. ► Reduction of metal ions can have important consequences in the study of soil chemistry.

Re-Os dating on pyrite and metal sources tracing in porphyry-type and neutral epithermal deposits: example of the Bolcana, Troita and Magura deposits, Apuseni Mountains, Romania

International Nuclear Information System (INIS)

Cardon, Olivier

2007-01-01

Many porphyry-type (Cu-Au) and neutral epithermal (Pb-Zn and Au ± Ag) ore deposits are encountered in the region of the Apuseni Mountains, located at the foot of the Carpathian chain in the Western Romania. These deposits are related to a Neogene andesitic volcanism. In order to demonstrate possible genetic relationships between the porphyry-type and neutral epithermal deposits, the Bolcana porphyry has been investigated since it is surrounded by a number of epithermal low-sulfidation veins with a Pb-Zn ± Au mineralisation. These veins are currently mined at the Troita and Magura sites. A structural analysis and a 3D modelling pf these deposits indicate that the geometry and orientation of fractures and mineralized vein are consistent both with direction of regional extension and with a NW-SE progression of the different andesitic intrusions. In order to establish precisely the temporal relationship between the different ore deposits, a Re-Os dating method has been developed and applied on pyrite which is ubiquitous in all of the deposits. This method enabled us to assign an age of 10.9 ± 1.9 Ma for the porphyry-hosted mineralization. The ages obtained for the epithermal systems are somewhat approximative as perturbations of the Re-Os system are observed for these environments. A fractionation of rhenium responsible for a significant enrichment in this element for the apical zone of the porphyry has been demonstrated. This enrichment is most probably related to a maximum boiling event, which may also explain a similar enrichment in arsenic for the pyrite in the same zone. The sources for the metals have been characterized at the district scale by combining two isotopic systems (Re-Os and Pb-Pb) on both pyrite and galena. The osmium data indicate that the Troita deposit has composition which is similar to that of the Bolcana porphyry. In contrast the results obtained for the Magura deposits indicate the Re-OS system has in this case been perturbed due to a

Microstructure evolution during 300 °C storage of sintered Ag nanoparticles on Ag and Au substrates

Energy Technology Data Exchange (ETDEWEB)

Paknejad, S.A. [King’s College London, Physics Department, Strand, London WC2R 2LS (United Kingdom); Dumas, G. [Eltek Semiconductors Ltd, Nelson Road Industrial Estate, Dartmouth, Devon TQ6 9LA (United Kingdom); West, G. [Loughborough University, Materials Department, Loughborough LE11 3TU (United Kingdom); Lewis, G. [Eltek Semiconductors Ltd, Nelson Road Industrial Estate, Dartmouth, Devon TQ6 9LA (United Kingdom); Mannan, S.H., E-mail: samjid.mannan@kcl.ac.uk [King’s College London, Physics Department, Strand, London WC2R 2LS (United Kingdom)

2014-12-25

Highlights: • Shear strength of pressure-free sintered Ag found to increase during ageing at 300 °C on Ag substrate. • Rapid collapse of void number density after 24 h ageing in the sintered Ag layer. • Higher porosity at edge of joint compared to the middle. • Shear strength of pressure-free sintered Ag decreases during ageing at 300 °C due to high porosity layer growth. • Void free layer and high porosity layer growth explained in terms of atomic diffusion and grain boundary migration. - Abstract: A silver nanoparticle based die attach material was used in a pressure free process to bond 2.5 mm square Ag plated Si die to Ag and Au plated substrates. The assemblies were stored at 300 °C for up to 500 h and the morphology of the sintered Ag and the shear strength were monitored as a function of time. On Ag substrate it was found that die shear strength increased and that the Ag grains grew in size and porosity decreased over time. There was also a clear difference in morphology between sintered Ag at the die edge and centre. On Au substrate, it was observed that the initially high die shear strength decreased with storage time and that voids migrated away from the Ag/Au interface and into the Ag joint. This has led to the formation of a void free layer at the interface followed by a high porosity region, which weakened the joint. The microstructure reveals a high density of grain and twin boundaries which facilitate the Ag and Au atomic diffusion responsible. The grain structure of the plated Au led to diffusion of Au into the Ag via high-angle tilt grain boundaries, and grain boundary migration further dispersed the Au into the Ag layer.

Site-Selective Carving and Co-Deposition: Transformation of Ag Nanocubes into Concave Nanocrystals Encased by Au-Ag Alloy Frames.

Science.gov (United States)

Ahn, Jaewan; Wang, Daniel; Ding, Yong; Zhang, Jiawei; Qin, Dong

2018-01-23

We report a facile synthesis of Ag nanocubes with concave side faces and Au-Ag alloy frames, namely Ag@Au-Ag concave nanocrystals, by titrating HAuCl 4 solution into an aqueous mixture of Ag nanocubes, ascorbic acid (H 2 Asc), NaOH, and cetyltrimethylammonium chloride (CTAC) at an initial pH of 11.6 under ambient conditions. Different from all previous studies involving poly(vinylpyrrolidine), the use of CTAC at a sufficiently high concentration plays an essential role in carving away Ag atoms from the side faces through galvanic replacement. Concurrent co-deposition of Au and Ag atoms via chemical reduction at orthogonal sites on the surface of Ag nanocubes leads to the generation of Ag@Au-Ag concave nanocrystals with well-defined and controllable structures. Specifically, in the presence of CTAC-derived Cl - ions, the titrated HAuCl 4 is maintained in the AuCl 4 - species, enabling its galvanic replacement with the Ag atoms located on the side faces of nanocubes. The released Ag + ions can be retained in the soluble form of AgCl 2 - by complexing with the Cl - ions. Both the AuCl 4 - and AgCl 2 - in the solution are then reduced by ascorbate monoanion, a product of the neutralization reaction between H 2 Asc and NaOH, to Au and Ag atoms for their preferential co-deposition onto the edges and corners of the Ag nanocubes. Compared with Ag nanocubes, the Ag@Au-Ag concave nanocrystals exhibit much stronger SERS activity at an excitation of 785 nm, making it feasible to monitor the Au-catalyzed reduction of 4-nitrothiophenol by NaBH 4 in situ. When the Ag cores are removed, the concave nanocrystals evolve into Au-Ag nanoframes with controllable ridge thicknesses.

Fabrication of Te and Te-Au Nanowires-Based Carbon Fiber Fabrics for Antibacterial Applications

Directory of Open Access Journals (Sweden)

Ting-Mao Chou

2016-02-01

Full Text Available Pathogenic bacteria that give rise to diseases every year remain a major health concern. In recent years, tellurium-based nanomaterials have been approved as new and efficient antibacterial agents. In this paper, we developed the approach to directly grow tellurium nanowires (Te NWs onto commercial carbon fiber fabrics and demonstrated their antibacterial activity. Those Te NWs can serve as templates and reducing agents for gold nanoparticles (Au NPs to deposit. Three different Te-Au NWs with varied concentration of Au NPs were synthesized and showed superior antibacterial activity and biocompability. These results indicate that the as-prepared carbon fiber fabrics with Te and Te-Au NWs can become antimicrobial clothing products in the near future.

Equilibrium phase diagram of the Ag-Au-Pb ternary system

International Nuclear Information System (INIS)

Hassam, S.; Bahari, Z.

2005-01-01

The phase diagram of the ternary system Ag-Au-Pb has been established using differential thermal analysis and X-ray powder diffraction analysis. Four vertical sections were studied: X Pb = 0.40, X Au /X Pb = 1/3, X Ag /X Au = 4/1 and X Ag /X Au = 1/1. Two ternary transitory peritectics and one ternary eutectic were characterized. A schematic representation of the ternary equilibria is given

Mineral types of hydrothermal alteration zones in the Dukat ore field and their relationships to leucogranite and epithermal gold-silver ore, northeastern Russia

Science.gov (United States)

Filimonova, L. G.; Trubkin, N. V.; Chugaev, A. V.

2014-05-01

The paper considers the localization of potassic and propylitic hydrothermal alteration zones in the domal volcanic-plutonic structure controlling the position of the Dukat ore field with the eponymous unique epithermal Au-Ag deposit. Comprehensive mineralogical and geochemical data on rocks and minerals in hydrothermal alteration zones and associated intrusions have shown that quartz-jarosite-sericite, quartz-pyrite-sericite, and quartz-adularia-chlorite alterations were formed with the participation of fluid flows related to a fingerlike projection of a high-K leucogranite porphyry intrusion with large phenocrysts. These hydrothermal alterations developed in the rifted graben under conditions of divergent plate boundaries, whereas quartz-clinozoisite-calcite, epidote-chlorite, and garnet-calcite-chlorite alterations were linked to K-Na leucogranite intrusive bodies and developed under conditions of convergent plate boundaries reactivated as a result of formation of the marginal Okhotsk-Chukotka volcanic belt. Phase separation and coagulation of specific portions of ascending fluids resulted in the formation and stabilization of small-sized particles of native silver and other ore components, which enabled involvement in flows of secondary geothermal solutions and ore-forming fluids. The Sr, Nd, and Pb isotopic compositions of rocks and minerals from the hydrothermal alteration zones, associated intrusions, and economic orebodies at the Dukat deposit indicate that their components have been derived from the juvenile continental crust, which was altered in pre-Cretaceous periods of endogenic activity. The components of gangue minerals of potassic and propylitic hydrothertmal alterations and associated intrusions have been taken from deep sources differing in 87Sr/86Sr and 143Nd/144Nd at similar U/Pb and Th/Pb ratios. Chalcophile lead in products of hydrothermal activity and melanocratic inclusions in leucogranite has been taken from regions with elevated U/Pb and

Comparison of Au and Ag nanoshells' metal-enhanced fluorescence

International Nuclear Information System (INIS)

Liaw, Jiunn-Woei; Chen, Huang-Chih; Kuo, Mao-Kuen

2014-01-01

The average enhancement factors of Au and Ag nanoshells (NSs) were analyzed theoretically to compare their overall performances on metal-enhanced fluorescence. We used the Mie theory and dyadic Green's functions to calculate the excitation rate and apparent quantum yield of NS interacting with a plane wave and a dipole, respectively, and then to obtain the enhancement factor. Moreover, the average enhancement factor (AEF) of NS on the fluorescence of a nearby molecule was obtained by averaging all possible orientations and locations of the molecule with a constant distance from NS. Our results show that the maximum AEF of Au NS occurs at the wavelength of the dipole mode, which is broadband. In contrast, the maximum AEF of Ag NS is at the narrowband quadrupole mode. In addition, the Stokes shift effect on AEF was studied for Au and Ag NSs. - Highlights: • The average enhancement factors of Au and Ag nanoshells were analyzed theoretically. • The maximum AEF of Au NS occurs at the wavelength of the dipole mode. • The maximum AEF of Ag NS is at the narrowband quadrupole mode. • The Stokes shift effect on AEF is discussed for Au and Ag NSs

Synthesis of biocompatible AuAgS/Ag2S nanoclusters and their applications in photocatalysis and mercury detection

International Nuclear Information System (INIS)

Zhao, Qian; Chen, Shenna; Zhang, Lingyang; Huang, Haowen; Liu, Fengping; Liu, Xuanyong

2014-01-01

In this paper, a facile approach for preparation of AuAgS/Ag 2 S nanoclusters was developed. The unique AuAgS/Ag 2 S nanoclusters capped with biomolecules exhibit interesting excellent optical and catalytic properties. The fluorescent AuAgS/Ag 2 S nanoclusters show tunable luminescence depending on the nanocluster size. The apoptosis assay demonstrated that the AuAgS/Ag 2 S nanoclusters showed low cytotoxicity and good biocompatibility. Therefore, the nanoclusters can be used not only as a probe for labeling cells but also for their photocatalytic activity for photodegradation of organic dye. Moreover, a highly selective and sensitive assay for detection of mercury including Hg 2+ and undissociated mercury complexes was developed based on the quenching fluorescent AuAgS/Ag 2 S nanoclusters, which provides a promising approach for determining various forms of Hg in the mercury-based compounds in environment. These unique nanoclusters may have potential applications in biological labeling, sensing mercury, and photodegradation of various organic pollutants in waste water.Graphical Abstract

Photoreduction of Ag{sup +} in Ag/Ag{sub 2}S/Au memristor

Energy Technology Data Exchange (ETDEWEB)

Mou, N.I.; Tabib-Azar, M., E-mail: azar.m@utah.edu

2015-06-15

Highlights: • The effect of illumination on the operating voltages and switching speed of Ag/Ag{sub 2}S/Au memristors is studied • Illumination decreased the average switching time from high to low resistance states by ∼19% and decreased the turn-off voltages dramatically from −0.8 V to −0.25 V. • Photo-induced reduction of silver in Ag{sub 2}S may be used in three dimensional optical memories that can be electronically read and reset. • Illumination changed sulfur's valency and modified its oxidation/reduction potential. - Abstract: Silver halides and chalcogenides are excellent memristor materials that have been extensively used in the past as photosensitive layers in photography. Here we examine the effect of illumination on the operating voltages and switching speed of Ag/Ag{sub 2}S/Au memristors using a green laser (473–523 nm). Our results indicate that illumination decreases the average switching time from high to low resistance states by ∼19% and decreases the turn-off voltages dramatically from −0.8 V to −0.25 V that we attribute to the change in sulfur valency and a photo-induced change in its oxidation/reduction potential. Photo-induced reduction of silver in Ag{sub 2}S may be used in three dimensional optical memories that can be electronically read and reset.

Thermodynamic assessment of the Ag-Te binary system

Energy Technology Data Exchange (ETDEWEB)

Gierlotka, Wojciech, E-mail: gilu@uci.agh.edu.p [Laboratory of Physical Chemistry and Electrochemistry, Faculty of Non-Ferrous Metals, AGH University of Science and Technology, 30 Mickiewicza Av., 30-059 Krakow (Poland)

2009-10-19

Pure silver and its alloys are very important materials for various technological applications. Tellurium is one of the unwanted admixture in silver and is removed during metallurgical processes; however Ag-Te alloy is necessary for production of rewritable digital versatile discs. The knowledge of phase diagram of Ag-Te is essential for applications and refining process. The critical assessment of binary system Ag-Te has been done using literature information. Good agreement between experimental data reported in literature and calculated values has been found.

Crystal and electronic structure study of AgAu and AgCu bimetallic alloy thin films by X-ray techniques

Energy Technology Data Exchange (ETDEWEB)

Ozkendir, O. Murat, E-mail: ozkendir@gmail.com [Mersin University, Faculty of Technology, Energy Systems Engineering, Tarsus (Turkey); Mersin University, Institute of Natural Science, Department of Nanotechnology and Advanced Materials, Mersin (Turkey); Cengiz, E. [Karadeniz Technical University, Faculty of Science, Department of Physics, Trabzon (Turkey); Yalaz, E. [Mersin University, Institute of Natural Science, Department of Nanotechnology and Advanced Materials, Mersin (Turkey); Söğüt, Ö.; Ayas, D.H. [Kahramanmaraş Sütçü İmam Üniversitesi, Faculty of Science and Letters, Department of Physics, Kahramanmaraş (Turkey); Thammajak, B. Nirawat [Synchrotron Light Research Institute (Public Organisation), 111 University Avenue, T. Suranaree, A. Muang, Nakhon Ratchasima 30000 (Thailand)

2016-05-15

Highlights: • Crystal and electronic properties of bimetallic AgCu and AgAu alloy thin films were studied. • Both AgCu and AgAu bimetallic samples were determined to have cubic crystal geometry. • Strong influence of Cu and Au atoms on the electronic structure of the Ag atoms were determined. - Abstract: Crystal and electronic structure properties of bimetallic AgAu and AgCu alloy thin films were investigated by X-ray spectroscopic techniques. The aim of this study is to probe the influence of Au or Cu atoms on the electronic behaviors of Ag ions in bimetallic alloy materials that yields different crystal properties. To identify the mechanisms causing crystal phase transitions, study were supported by the collected EXAFS (Extended X-ray Absorption Fine Structure) data. Crystal structures of both Cu and Au doped bimetallic Ag samples were determined mainly in cubic geometry with “Fm3m” space group. Through the Ag–Au and Ag–Cu molecular interactions during bimetallic alloy formations, highly overlapped electronic levels that supports large molecular band formations were observed with different ionization states. Besides, traces of the d–d interactions in Au rich samples were determined as the main interplay in the broad molecular bond formations. The exact atomic locations and types in the samples were determined by EXAFS studies and supported by the performed calculations with FEFF scientific code.

Hydrothermal Synthesis and Mechanism of Unusual Zigzag Ag2Te and Ag2Te/C Core-Shell Nanostructures

Directory of Open Access Journals (Sweden)

Saima Manzoor

2014-01-01

Full Text Available A single step surfactant-assisted hydrothermal route has been developed for the synthesis of zigzag silver telluride nanowires with diameter of 50–60 nm and length of several tens of micrometers. Silver nitrate (AgNO3 and sodium tellurite (Na2TeO3, are the precursors and polyvinylpyrrolidone (PVP is used as surfactant in the presence of the reducing agent, that is, hydrazine hydrate (N2H4·H2O. In addition to the zigzag nanowires a facile hydrothermal reduction-carbonization route is proposed for the preparation of uniform core-shell Ag2Te/C nanowires. In case of Ag2Te/C synthesis process the same precursors are employed for Ag and Te along with the ethylene glycol used as reducing agent and glucose as the carbonizing agent. Morphological and compositional properties of the prepared products are analyzed with the help of scanning electron microscopy, transmission electron microscopy, and energy dispersive X-ray spectroscopy, respectively. The detailed formation mechanism of the zigzag morphology and reduction-carbonization growth mechanism for core-shell nanowires are illustrated on the bases of experimental results.

Enhanced catalyst activity by decorating of Au on Ag@Cu2O nanoshell

Science.gov (United States)

Chen, Lei; Liu, Maomao; Zhao, Yue; Kou, Qiangwei; Wang, Yaxin; Liu, Yang; Zhang, Yongjun; Yang, Jinghai; Jung, Young Mee

2018-03-01

We successfully synthesized Au-decorated Ag@Cu2O heterostructures via a simple galvanic replacement method. As the Au precursor concentration increased, the density of the Au nanoparticles (NPs) on the Ag@Cu2O surface increased, which changed the catalytic activity of the Ag@Cu2O-Au structure. The combination of Au, Ag, and Cu2O exhibited excellent catalytic properties, which can further effect on the catalyst activity of the Ag@Cu2O-Au structure. In addition, the proposed Ag@Cu2O-Au nanocomposite was used to transform the organic, toxic pollutant, 4-nitrophenol (4-NP), into its nontoxic and medicinally important amino derivative via a catalytic reduction to optimize the material performance. The proposed Au-decorated Ag@Cu2O exhibited excellent catalytic activity, and the catalytic reduction time greatly decreased (5 min). Thus, three novel properties of Ag@Cu2O-Au, i.e., charge redistribution and transfer, adsorption, and catalytic reduction of organic pollutants, were ascertained for water remediation. The proposed catalytic properties have potential applications for photocatalysis and localized surface plasmon resonance (LSPR)- and peroxidase-like catalysis.

New chalcogenide glasses in the CdTe-AgI-As{sub 2}Te{sub 3} system

Energy Technology Data Exchange (ETDEWEB)

Kassem, M. [Univ. Picardie Jules Verne, F-80000 Amiens (France); Le Coq, D., E-mail: david.lecoq@univ-littoral.fr [Univ. Lille Nord de France, F-59000 Lille (France); ULCO, LPCA, EA 4493, F-59140 Dunkerque (France); Boidin, R.; Bychkov, E. [Univ. Lille Nord de France, F-59000 Lille (France); ULCO, LPCA, EA 4493, F-59140 Dunkerque (France)

2012-02-15

Highlights: Black-Right-Pointing-Pointer Determination of the glass-forming region in the pseudo-ternary CdTe-AgI-As{sub 2}Te{sub 3} system. Black-Right-Pointing-Pointer Characterization of macroscopic properties of the new CdTe-AgI-As{sub 2}Te{sub 3} glasses. Black-Right-Pointing-Pointer Characterization of the total conductivity of CdTe-AgI-As{sub 2}Te{sub 3} glasses. Black-Right-Pointing-Pointer Comparison between the selenide and telluride equivalent systems. -- Abstract: Chalcogenide glasses in the pseudo-ternary CdTe-AgI-As{sub 2}Te{sub 3} system were synthesized and the glass-forming range was determined. The maximum content of CdTe in this glass system was found to be equal to 15 mol.%. The macroscopic characterizations of samples have consisted in Differential Scanning Calorimetry, density, and X-ray diffraction measurements. The cadmium telluride addition does not generate any significant change in the glass transition temperature but the resistance of binary AgI-As{sub 2}Te{sub 3} glasses towards crystallisation is estimated to be decreasing on the base of {Delta}T = T{sub x} - T{sub g} parameter. The total electrical conductivity {sigma} was measured by complex impedance spectroscopy. First, the CdTe additions in the (AgI){sub 0.5}(As{sub 2}Te{sub 3}){sub 0.5} host glass, (CdTe){sub x}(AgI){sub 0.5-x/2}(As{sub 2}Te{sub 3}){sub 0.5-x/2} lead to a conductivity decrease at x {<=} 0.05. Then, the behaviour is reversed at 0.05 {<=} x {<=} 0.15. The obtained results are discussed by comparison with the equivalent selenide system.

Formation of Ag2, Au2 and AgAu particles on MgO(1 0 0): DFT study on the role of support-induced charge transfer in metal-metal interactions

International Nuclear Information System (INIS)

Fuente, Silvia A.; Belelli, Patricia G.; Branda, Maria M.; Ferullo, Ricardo M.; Castellani, Norberto J.

2009-01-01

The formation of Ag 2 , Au 2 and AgAu particles oriented perpendicularly to the MgO(1 0 0) surface was studied using the density functional theory. While the support induces a slight enhancement of the Ag-Ag bond (by 0.3-0.4 eV), the Au-Au bond is strongly enhanced (by 0.8-1.1 eV). Concerning the bimetallic particle, the Ag-Au bond stabilization depends on the relative position of each atom. Thus, in general terms, the strength of the metal-metal bond is determined by the nature of the terminal atom; the bond is stronger in Au-terminal particles. The partial electronic charge transfer to the terminal Au atom and its ability to polarize this charge are responsible for this energetic stabilization.

Toward hybrid Au nanorods @ M (Au, Ag, Pd and Pt) core-shell heterostructures for ultrasensitive SERS probes

Science.gov (United States)

Xie, Xiaobin; Gao, Guanhui; Kang, Shendong; Lei, Yanhua; Pan, Zhengyin; Shibayama, Tamaki; Cai, Lintao

2017-06-01

Being able to precisely control the morphologies of noble metallic nanostructures is of essential significance for promoting the surface-enhanced Raman scattering (SERS) effect. Herein, we demonstrate an overgrowth strategy for synthesizing Au @ M (M = Au, Ag, Pd, Pt) core-shell heterogeneous nanocrystals with an orientated structural evolution and highly improved properties by using Au nanorods as seeds. With the same reaction condition system applied, we obtain four well-designed heterostructures with diverse shapes, including Au concave nanocuboids (Au CNs), Au @ Ag crystalizing face central cube nanopeanuts, Au @ Pd porous nanocuboids and Au @ Pt nanotrepangs. Subsequently, the exact overgrowth mechanism of the above heterostructural building blocks is further analysed via the systematic optimiziation of a series of fabrications. Remarkably, the well-defined Au CNs and Au @ Ag nanopeanuts both exhibit highly promoted SERS activity. We expect to be able to supply a facile strategy for the fabrication of multimetallic heterogeneous nanostructures, exploring the high SERS effect and catalytic activities.

Preparation of Ag{sub core}/Au{sub shell} bimetallic nanoparticles from physical mixtures of Au clusters and Ag ions under dark conditions and their catalytic activity for aerobic glucose oxidation

Energy Technology Data Exchange (ETDEWEB)

Zhang, Haijun, E-mail: zhanghaijun@wust.edu.cn [College of Materials and Metallurgy, Wuhan University of Science and Technology, Wuhan, Hubei Province 430081 (China); Toshima, Naoki; Takasaki, Kanako [Department of Applied Chemistry, Tokyo University of Science Yamaguchi, SanyoOnoda-shi, Yamaguchi 756-0884 (Japan); Okumura, Mitsutaka [Department of Chemistry, Graduate School of Science, Osaka University, Machikaneyama, Toyonaka, Osaka 560-0043 (Japan)

2014-02-15

Graphical abstract: The synthesis, characterization and catalytic activities for glucose oxidation of AgAu bimetallic nanoparticles (BNPs) with size of less than 2 nm are reported. The catalytic activity of Ag{sub 10}Au{sub 90} BNPs was about two times higher than that of Au NPs, even the BNPs have a larger particle size than that of Au NPs. -- Highlights: • Ag{sub core}/Au{sub shell} BNPs with size of less than 2.0 nm were prepared. • No any reducing reagents and lights were used for the preparation of the BNPs. • The catalytic activity of the BNPs is about two times higher than that of Au NPs. -- Abstract: AgAu bimetallic nanoparticles (BNPs), one of the most extensively studied bimetallic systems in the literatures, could have various structures and compositions depending on their preparation conditions. In the present work, catalytically highly active PVP-protected Ag{sub core}/Au{sub shell} BNPs of about 2.5 nm in diameter were fabricated from physical mixtures of aqueous dispersions of Au nanoparticles and Ag{sup +} ions under dark conditions without using any reducing agents. The prepared Ag{sub core}/Au{sub shell} BNP colloidal catalysts, which possessed a high activity for aerobic glucose oxidation, were characterized by Ultraviolet–visible spectrophotometry (UV–Vis), Inductive coupled plasma emission spectrometer (ICP), Transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and Energy disperse spectroscopy (EDS) in High-resolution scanning transmission electron microscopy (HR-STEM). The highest activity (11,360 mol-glucose h{sup −1} mol-metal{sup −1}) was observed for the BNPs with the Ag/Au atomic ratio of 1/9, the TOF value of which is about two times higher than that of Au nanoparticles with the particle size of 1.3 nm. The enhanced catalytic activity of the prepared Ag{sub core}/Au{sub shell} BNPs compared to Au NPs can be ascribed to the presence of negatively charged Au atoms resulted from electron donations

Plasmon enhanced water splitting mediated by hybrid bimetallic Au-Ag core-shell nanostructures.

Science.gov (United States)

Erwin, William R; Coppola, Andrew; Zarick, Holly F; Arora, Poorva; Miller, Kevin J; Bardhan, Rizia

2014-11-07

In this work, we employed wet chemically synthesized bimetallic Au-Ag core-shell nanostructures (Au-AgNSs) to enhance the photocurrent density of mesoporous TiO2 for water splitting and we compared the results with monometallic Au nanoparticles (AuNPs). While Au-AgNSs incorporated photoanodes give rise to 14× enhancement in incident photon to charge carrier efficiency, AuNPs embedded photoanodes result in 6× enhancement. By varying nanoparticle concentration in the photoanodes, we observed ∼245× less Au-AgNSs are required relative to AuNPs to generate similar photocurrent enhancement for solar fuel conversion. Power-dependent measurements of Au-AgNSs and AuNPs showed a first order dependence to incident light intensity, relative to half-order dependence for TiO2 only photoanodes. This indicated that plasmonic nanostructures enhance charge carriers formed on the surface of the TiO2 which effectively participate in photochemical reactions. Our experiments and simulations suggest the enhanced near-field, far-field, and multipolar resonances of Au-AgNSs facilitating broadband absorption of solar radiation collectively gives rise to their superior performance in water splitting.

Picosecond laser fabricated Ag, Au and Ag-Au nanoparticles for detecting ammonium perchlorate using a portable Raman spectrometer

Science.gov (United States)

Byram, Chandu; Moram, Sree Sathya Bharathi; Soma, Venugopal Rao

2018-04-01

In this paper, we present the results from fabrication studies of Ag, Au, and Ag-Au alloy nanoparticles (NPs) using picosecond laser ablation technique in the presence of liquid media. The alloy formation in the NPs was confirmed from UV-Visible measurements. The shape and crystallinity of NPs were investigated by using high resolution transmission electron microscopy (HRTEM), selected area diffraction pattern (SAED) and energy dispersive spectroscopy (EDS). The SERS effect of fabricated NPs was tested with methylene blue and an explosive molecule (ammonium perchlorate) using a portable Raman spectrometer and achieved EFs of ˜106.

Computational investigation of CO adsorbed on Aux, Agx and (AuAg)x nanoclusters (x = 1 - 5, 147) and monometallic Au and Ag low-energy surfaces*

Science.gov (United States)

Gould, Anna L.; Catlow, C. Richard A.; Logsdail, Andrew J.

2018-02-01

Density functional theory calculations have been performed to investigate the use of CO as a probe molecule for the determination of the structure and composition of Au, Ag and AuAg nanoparticles. For very small nanoclusters (x = 1 - 5), the CO vibrational frequencies can be directly correlated to CO adsorption strength, whereas larger 147-atom nanoparticles show a strong energetic preference for CO adsorption at a vertex position but the highest wavenumbers are for the bridge positions. We also studied CO adsorption on Au and Ag (100) and (111) surfaces, for a 1 monolayer coverage, which proves to be energetically favourable on atop only and bridge positions for Au (100) and atop for Ag (100); vibrational frequencies of the CO molecules red-shift to lower wavenumbers as a result of increased metal coordination. We conclude that CO vibrational frequencies cannot be solely relied upon in order to obtain accurate compositional analysis, but we do propose that elemental rearrangement in the core@shell nanoclusters, from Ag@Au (or Au@Ag) to an alloy, would result in a shift in the CO vibrational frequencies that indicate changes in the surface composition. Contribution to the Topical Issue "Shaping Nanocatalysts", edited by Francesca Baletto, Roy L. Johnston, Jochen Blumberger and Alex Shluger.Supplementary material in the form of one pdf file available from the Journal web page at http://https://doi.org/10.1140/epjb/e2017-80280-7

Geologic setting and genesis of the Mule Canyon low-sulfidation epithermal gold-silver deposit, north-central Nevada

Science.gov (United States)

John, D.A.; Hofstra, A.H.; Fleck, R.J.; Brummer, J.E.; Saderholm, E.C.

2003-01-01

The Mule Canyon mine exploited shallow, low-sulfidation, epithermal Au-Ag deposits that lie near the west side of the Northern Nevada rift in northern Lander County, Nevada. Mule Canyon consists of six small deposits that contained premining reserves of about 8.2 Mt at an average grade of 3.81 g Au/tonne. It is an uncommon mafic end member of low-sulfidation Au-Ag deposits associated with tholeiitic bimodal basalt-rhyolite magmatism. The ore is hosted by a basalt-andesite eruptive center that formed between about 16.4 to 15.8 Ma during early mafic eruptions related to regionally extensive bimodal magmatism. Hydrothermal alteration and Au-Ag ores formed at about 15.6 Ma and were tightly controlled by north-northwest- to north-striking high-angle fault and breccia zones developed during rifting, emplacement of mafic dikes, and eruption of mafic lava flows. Hydrothermal alteration assemblages are zoned outward from fluid conduits in the sequence silica-adularia, adularia-smectite, smectite (intermediate argillic), and smectite-carbonate (propylitic). All alteration types contain abundant pyrite and/or marcasite ?? arsenopyrite. Field relations indicate that silica-adularia alteration is superimposed on argillic and propylitic alteration. Little or no steam-heated acid-sulfate alteration is present, probably the result of a near-surface water table during hydrothermal alteration and ore deposition. Two distinct ore types are present at Mule Canyon: early replacement and later open-space filling. Replacement ores consist of disseminated and vesicle-filling pyrite, marcasite, and arsenopyrite in argillically altered or weakly silicified rocks. Ore minerals consist of Au-bearing arsenopyrite and arsenian pyrite overgrowths on earlier-formed pyrite and marcasite. Open-space filling ores include narrow stockwork quartz-adularia veins, banded and crustiform opaline and chalcedonic silica-adularia veins, silica-adularia cemented breccias, and sparse carbonate-pyrite and

Evolution of the Bucium Rodu and Frasin magmatic-hydrothermal system, Metaliferi Mountains, Romania

Science.gov (United States)

Iatan, Elena Luisa; Berbeleac, Ion; Visan, Madalina; Minut, Adrian; Nadasan, Laurentiu

2013-04-01

The Miocene Bucium Rodu and Frasin maar-diatreme structures and related Au-Ag epithermal low sulfidation with passing to mesothermal mineralizations are located in the Bucium-Rosia Montana-Baia de Aries metallogenetic district, within so called the "Golden Quatrilaterum", in the northeastern part of the Metaliferi Mountains. These structures are situated at about 5 km southeast from Rosia Montana, the largest European Au-Ag deposit. The total reserves for Bucium Rodu-Frasin are estimated at 43.3 Mt with average contents of 1.3 g/t Au and 3 g/t Ag. The Miocene geological evolution of Bucium Rodu and Frasin magmatic-hydrothermal system took place in closely relationships with tectonic, magmatic and metallogenetic activity from Bucium-Rosia Montana-Baia de Aries district in general, and adjacent areas, in special. The hydrothermal alteration is pervasive; adularia followed by phyllic, carbonatization and silicification alterations, usually show a close relationship with the mineralizations. Propylitic alteration occurs dominantly towards the depth; argillic alteration shows a local character. The mineralization occurs in veins, breccias, stockworks and disseminations and is hosted within two volcanic structures emplaced into a sequence of Cretaceous sediments in closely genetically relations with the Miocene phreatomagmatic fracturing and brecciation events. Within Rodu maar-diatreme structure the mineralizations follow especially the contact between the diatreme and Cretaceous flysch. The vein sets with low, moderately and near vertical dippings, cover 400x400m with N-S trend. The most important mineralization style is represented by veins, accompanied by hydrothermal breccias and disseminations. The veins spatial distribution relives as "en echelon" tension veins. They carry gold, minor base metal sulphides (pyrite, chalcopyrite, sphalerite, galena, tetrahedrite, arsenopyrite). Gangue is represented by carbonates (calcite, dolomite, ankerite, siderite, rhodochrosite

Measurement of epithermal neutrons by a coherent demodulation technique

CERN Document Server

Horiuchi, N; Takahashi, H; Kobayashi, H; Harasawa, S

2000-01-01

Epithermal neutrons have been measured using a neutron dosimeter via a coherent demodulation technique. This dosimeter consists of CsI(Tl)-photodiode scintillation detectors, four of which are coupled to neutron-gamma converting foils of various sizes. Neutron-gamma converting foils of In, Au and Co materials were used, each of which has a large capture cross section which peaks in the epithermal neutron energy region. The type of foil was selected according to the material properties that best correspond to the energy of the epithermal neutrons to be measured. In addition, the proposed technique was applied using Au-foils in order to measure the Cd ratio. The validity of the proposed technique was examined using an sup 2 sup 4 sup 1 Am-Be source placed in a testing stack of polyethylene blocks, and the results were compared with the theoretical values calculated by the Monte Carlo calculation. Finally, the dosimeter was applied for measuring epithermal neutrons and the Cd ratio in an experimental beam-tube o...

The genesis of the slab window-related Arzular low-sulfidation epithermal gold mineralization (eastern Pontides, NE Turkey

Directory of Open Access Journals (Sweden)

Enver Akaryalı

2013-07-01

Full Text Available The Arzular mineralization is one of the best examples of epithermal gold deposits in the eastern Pontides orogenic belt. The mineralization is hosted by the subduction-related basaltic andesites and is mainly controlled by E–W and NE–SW trending fracture zones. The main ore minerals are galena, sphalerite, pyrite, chalcopyrite, tetrahedrite and gold. Homogenization temperatures of fluid inclusions are between 130 and 295 °C for quartz and between 90 and 133 °C for sphalerite. Sulphur isotope values obtained from pyrite, galena and sphalerite vary between −1.2‰ and 3‰, indicating that sulphur belongs to magmatic origin and was derived from the Lutetian non-adakitic granitic intrusions in the region. Oxygen isotope values are between 15.0‰ and 16.7‰, and hydrogen isotope values are between −87‰ and −91‰. The sulphur isotope thermometer yielded temperatures in the range of 244–291 °C for the ore formation. Our results support the hypothesis that the Arzular mineralization is a low-sulfidation epithermal gold deposit associated with non-adakitic subduction-related granitic magmas that were generated by slab window-related processes in a south-dipping subduction zone during the Lutetian.

Novel condensation of Au-centered trigonal prisms in rare-earth-metal-rich tellurides: Er7Au2Te2 and Lu7Au2Te2.

Science.gov (United States)

Gupta, Shalabh; Corbett, John D

2010-07-14

A new monoclinic structure occurs for Er(7)Au(2)Te(2) according to X-ray diffraction analysis of single crystals grown at 1200 degrees C: C2/m, Z = 4, a = 17.8310(9) A, b = 3.9819(5) A, c = 16.9089(9) A, beta = 104.361(4) degrees. The isostructural Lu(7)Au(2)Te(2) also exists according to X-ray powder pattern means, a = 17.536(4) A, b = 3.9719(4) A, c = 16.695(2) A, beta = 104.33(1) degrees. The structure contains zigzag chains of condensed, Au-centered tricapped trigonal prisms (TCTP) of Er along c that also share basal faces along b to generate puckered sheets. Further bi-face-capping Er atoms between these generate the three dimensional network along a, with tellurium in cavities outlined by augmented trigonal prismatic Er polyhedra. Bonding analysis via LMTO-DFT methods reveal very significant Er-Au bonding interactions, as quantified by their energy-weighted Hamilton overlap populations (-ICOHP), approximately 49% of the total for all interactions. These and similar Er-Te contributions sharply contrast with the small Er-Er population, only approximately 14% of the total in spite of the high proportion of Er-Er contacts. The strong polar bonding of Er to the electronegative Au and Te leaves Er relatively oxidized, with many of its 5d states falling above the Fermi level and empty. The contradiction with customary representations of structures that highlight rare-earth metal clusters is manifest. The large Er-Au Hamilton overlap population is in accord with the strong bonding between early and late transition metals first noted by Brewer in 1973. The relationship of this structure to the more distorted orthorhombic (Imm2) structure type of neighboring Dy(7)Ir(2)Te(2) is considered.

Mineralogy, structural control and age of the Incachule Sb epithermal veins, the Cerro Aguas Calientes collapse caldera, Central Puna

Science.gov (United States)

Salado Paz, Natalia; Petrinovic, Iván; Do Campo, Margarita; Brod, José Affonso; Nieto, Fernando; da Silva Souza, Valmir; Wemmer, Klauss; Payrola, Patricio; Ventura, Roberto

2018-03-01

The Incachule Sb epithermal veins is located near to the N-E rim of the Cerro Aguas Calientes collapse caldera (17.5-10.8 Ma), in the geologic province of Puna, Salta- Argentina. It is hosted in Miocene felsic volcanic rocks with continental arc signature. The district includes twelve vein systems with mineralization of Sb occurring in hydrothermal breccias and stockwork. The veins are composed of quartz-sulfide with pyrite, stibnite and arsenopyrite. All around the veins, wall rocks are variably altered to clay minerals and sulfates in an area of around 2.5 km wide by more than 7 km long. The hydrothermal alterations recognized are: silicic, phyllic and argillic. The veins are characterized by high contents of Sb, As, and Tl and intermediate contents of Pb-Zn-Cu, and traces of Ag and Au. Homogenization and ice-melting temperatures of fluid inclusions vary from 125 °C to 189 °C and -2.4 °C to -0.8 °C. The isotopic data indicated a range of δ34S -3.04‰ to +0.72‰ consistent with a magmatic source for sulfur. We present the firsts K-Ar ages for hydrothermal illite/smectite mixed layers (I/SR1, 60% illite layers) and illite that constrain the age of the ore deposit (8.5-6.7 ± 0.2 Ma). The data shown here, let characterized the Incachule district as a shallow low sulfidation epithermal system hosted in a collapse caldera. Our data also indicate that mineralization is structurally controlled by a fault system related to the 10.3 Ma collapse of Aguas Calientes caldera. The interpreted local stress field is consistent with the regional one.

Fabrication of fine spongy nanoporous Ag-Au alloys with improved catalysis properties

Directory of Open Access Journals (Sweden)

Cuiting Li

2017-12-01

Full Text Available Fine NP-AgAu (nanoporous AgAu alloys with spongy structure was fabricated by chemical dealloying from rapidly solidified amorphous precursors Ag38.75−xCu38.75Si22.5Aux (x=0, 0.5, 1 and 5. The results indicate that the addition of small content Au in precursor can refine both the ligaments and pores obviously. Among the present components of the precursors, NP-AgAu alloys dealloying from Ag37.75Cu38.75Si22.5Au1 had the finest spongy structure. The size of pores was 5–10 nm and the grain size of ligaments was 10–20 nm. It also had the highest surface area of 106.83 m2g−1 and the best catalytic activity towards electro-oxidation of formaldehyde with the peak current of 665 mA mg−1.

Comparative efficiencies of photothermal destruction of malignant cells using antibody-coated silica-Au nanoshells, hollow Au/Ag nanospheres and Au nanorods

Energy Technology Data Exchange (ETDEWEB)

Cheng, Fong-Yu; Chen, Chen-Tai; Yeh, Chen-Sheng, E-mail: csyeh@mail.ncku.edu.t [Department of Chemistry, National Cheng Kung University, Tainan 701, Taiwan (China)

2009-10-21

Three Au-based nanomaterials (silica-Au nanoshells, hollow Au/Ag nanospheres and Au nanorods) were evaluated for their comparative photothermal efficiencies at killing three types of malignant cells (A549 lung cancer cells, HeLa cervix cancer cells and TCC bladder cancer cells) using a CW NIR laser. Photodestructive efficiency was evaluated as a function of the number of nanoparticles required to destroy the cancer cells under 808 nm laser wavelength at fixed laser power. Of the three nanomaterials, silica/Au nanoshells needed the minimum number of particles to produce effective photodestruction, whereas Au nanorods needed the largest number of particles. Together with the calculated photothermal conversion efficiency, the photothermal efficiency rankings are silica-Au nanoshells > hollow Au/Ag nanospheres > Au nanorods. Additionally, we found that HeLa cells seem to present better heat tolerance than the other two cancer cell lines.

Studies on L-histidine capped Ag and Au nanoparticles for dopamine detection

Energy Technology Data Exchange (ETDEWEB)

Nivedhini Iswarya, Chandrasekaran; Kiruba Daniel, S.C.G. [Division of Nanoscience and Technology, Anna University-BIT Campus, Tiruchirappalli 620024 (India); Sivakumar, Muthusamy, E-mail: muthusiva@gmail.com [Division of Nanoscience and Technology, Anna University-BIT Campus, Tiruchirappalli 620024 (India); Department of Chemistry, Anna University-BIT Campus, Tiruchirappalli 620024 (India)

2017-06-01

This work demonstrates the effective surface functionalization of Ag, Au and bimetallic Ag-Au nanoparticles using L-histidine for colorimetric detection of dopamine (DA) which plays majorly in recognizing the neurological disorder. L-Histidine (L-His) capped Ag, Au, and bimetallic Ag-Au nanoparticles are characterized using physico-chemical techniques. The optical behaviour of nanoparticles has been analysed at various time intervals using UV–Vis absorption spectroscopy. FT-IR results provide the evidence of chemical bonding between L-histidine and metal nanoparticles. Its structure with the capping of L-His was clearly shown in HR-TEM images. The average size of nanoparticles has calculated from TEM image fringes are 11 nm, 5 nm and 6.5 nm respectively, matches with crystals size calculated from X-ray diffraction pattern. Enhanced optical nature of nanoparticles provides the best platform to develop a colorimetric-based biosensor for DA detection. After addition of DA, a rapid colour change has been noted in colloids of nanoparticles. The substantial changes in absorbance and λ{sub max} in metal nanoparticles respect to DA concentration have been observed and formulated. This is one of the successive methods for trace level determination of DA and will be going to a significant material for designing biosensor to determine DA in real extracellular body fluids. - Highlights: • L-His functionalized Ag, Au and bimetallic Ag-Au nanoparticles were prepared and its properties were studied. • L-His based Ag, Au, Ag-Au nanoparticles have characterized by spectroscopy, XRD and microscopic studies. • Enhanced optical nature of nanoparticles delivers the best platform to develop a biosensor for DA detection. • For qualitative determination of dopamine, SPR of metal nanoparticles plays a major role in dopamine determination. • This basic finding can be utilized for further identification of imbalanced DA concentration in body fluids.

Ionic-to-Electronic Conductivity Crossover in CdTe-AgI-As2Te3 Glasses: An 110mAg Tracer Diffusion Study.

Science.gov (United States)

Kassem, M; Alekseev, I; Bokova, M; Le Coq, D; Bychkov, E

2018-04-12

Conductivity isotherms of (CdTe) x (AgI) 0.5- x/2 (As 2 Te 3 ) 0.5- x/2 glasses (0.0 ≤ x ≤ 0.15) reveal a nonmonotonic behavior with increasing CdTe content reminiscent of mixed cation effect in oxide and chalcogenide glasses. Nevertheless, the apparent similarity appears to be partly incorrect. Using 110m Ag tracer diffusion measurements, we show that semiconducting CdTe additions produce a dual effect: (i) decreasing the Ag + ion transport by a factor of ≈200 with a simultaneous increase of the diffusion activation energy and (ii) increasing the electronic conductivity by 1.5 orders of magnitude. Consequently, the conductivity minimum at x = 0.05 reflects an ionic-to-electronic transport crossover; the silver-ion transport number decreases by 3 orders of magnitude with increasing x.

Direct measurement of time dependent diffusion for Ag and Au under ambient conditions

Energy Technology Data Exchange (ETDEWEB)

Yoo, Pil Sun; Jo, Han Yeol; Kim, Tae Kyeong [Hankuk University of Foreign Studies, Yongin (Korea, Republic of)

2014-12-15

Time-dependent diffusion for Ag and Au metal atoms was measured using the scanning tunneling microscope break-junction technique in ambient conditions. We observed that Ag contacts do not form long single-atomic chains compared to Au contacts during the elongation of each metal electrode, and Ag atoms diffuse more quickly than Au atoms after metal contact rupture. This is consistent with previous results of molecular dynamic simulations. Further, we found a correlation between diffusion length and the evolution time on an atomic scale to reveal the time-dependent diffusion for Ag and Au metal atoms.

The crystal structure of TeCl3+AuCl4-

International Nuclear Information System (INIS)

Jones, P.G.; Jentsch, D.; Schwarzmann, E.

1986-01-01

TeCl 3 + AuCl 4 - crystallizes in the triclinic space group Panti 1 with a=7.564(2), b=7.720(3), c=8.964(3) A, α=78.26(3), β=88.84(3), γ=89.35(3) 0 , Z=2. The structure was refined to R 0.041 for 1380 reflections. The cation polyhedron, including secondary Te...Cl interactions, is a square pyramid with mean Te-Cl 2.294, Te...Cl 3.028 A. The secondary interactions link the ions to form centrosymmetric (TeCl 3 .AuCl 4 ) 2 dimers. (orig.)

First evidence of epithermal gold occurrences in the SE Afar Rift, Republic of Djibouti

Science.gov (United States)

Moussa, N.; Fouquet, Y.; Le Gall, B.; Caminiti, A. M.; Rolet, J.; Bohn, M.; Etoubleau, J.; Delacourt, C.; Jalludin, M.

2012-06-01

The geology of the Republic of Djibouti, in the SE Afar Triangle, is characterized by intense tectonic and bimodal volcanic activity that began as early as 25-30 Ma. Each magmatic event was accompanied by hydrothermal activity. Mineralization generally occurs as gold-silver bearing chalcedony veins and is associated with felsic volcanism. Eighty samples from mineralized hydrothermal chalcedony, quartz ± carbonate veins and breccias were studied from ten sites representing four major volcanic events that range in age from early Miocene to the present. The most recent veins are controlled by fractures at the edges of grabens established during the last 4 Myr. Gold in excess of 200 ppb is present in 30% of the samples, with values up to 16 ppm. Mineralogical compositions allowed us to identify different types of mineralization corresponding to different depths in the hydrothermal system: (1) surface and subsurface mineralization characterized by carbonate chimneys, gypsum, silica cap and quartz ± carbonate veins that are depleted in metals and Au; (2) shallow banded chalcedony ± adularia veins related to boiling that contain up to 16 ppm Au, occurring as native gold and electrum with pyrite, and tetradymite; (3) quartz veins with sulfides, and (4) epidote alteration in the deepest hydrothermal zones. Samples in which pyrite is enriched in As tend to have a high Au content. The association with bimodal volcanism, the occurrence of adularia and the native Au and electrum in banded chalcedony veins are typical of epithermal systems and confirm that this type of mineralization can occur in a young intracontinental rift system.

TEM and TED investigation of Ag/PbTe thin film bilayers.

Science.gov (United States)

Mandrino, Đorđe; Marinković, V.

Morphology and phase structure of Ag/PbTe thin film bilayers were investigated. This system was of particular interest because of interfacial reaction observed previously in an analogous Ag/SnTe system. Reaction products due to the interdiffusion of Ag with the substrate were determined as well as their orientations. They were discussed in view of the reaction products' structural relations to the PbTe.

Thermal stability of substitutional ag in CdTe

NARCIS (Netherlands)

Jahn, SG; Hofsass, H; Restle, M; Ronning, C; Quintel, H; BharuthRam, K; Wahl, U

The thermal stability of substitutional Ag in CdTe was deduced from lattice location measurements at different temperatures. Substitutional Ag probe atoms were generated via transmutation doping from radioactive Cd isotopes. The lattice sites of Ag isotopes were determined by measuring the

Strain Distribution of Au and Ag Nanoparticles Embedded in Al2O3 Thin Film

Directory of Open Access Journals (Sweden)

Honghua Huang

2014-01-01

Full Text Available Au and Ag nanoparticles embedded in amorphous Al2O3 matrix are fabricated by the pulsed laser deposition (PLD method and rapid thermal annealing (RTA technique, which are confirmed by the experimental high-resolution transmission electron microscope (HRTEM results, respectively. The strain distribution of Au and Ag nanoparticles embedded in the Al2O3 matrix is investigated by the finite-element (FE calculations. The simulation results clearly indicate that both the Au and Ag nanoparticles incur compressive strain by the Al2O3 matrix. However, the compressive strain existing on the Au nanoparticle is much weaker than that on the Ag nanoparticle. This phenomenon can be attributed to the reason that Young’s modulus of Au is larger than that of Ag. This different strain distribution of Au and Ag nanoparticles in the same host matrix may have a significant influence on the technological potential applications of the Au-Ag alloy nanoparticles.

A novel intermediate layer for Au/CdZnTe/FTO photoconductive structure

Energy Technology Data Exchange (ETDEWEB)

Zhang, Yuelu; Wang, Linjun, E-mail: ljwang@shu.edu.cn; Xu, Run; Huang, Jian; Tao, Jun; Meng, Hua; Zhang, Jijun; Min, Jiahua

2016-12-01

Highlights: • Graphene layer was spin-coated on CdZnTe to form Au/graphene/CdZnTe/FTO structure. • Graphene layer can significantly improve the contact property of Au/CdZnTe. • Graphene layer can obviously enhance UV photo-response of CdZnTe. • Graphene is a potential buffer material for CdZnTe based high-energy detectors. - Abstract: In this work, graphene is tried to use to improve the performance of polycrystalline CdZnTe high-energy radiation and photon detectors. A graphene intermediate layer is prepared by spin-coating process on the surface of polycrystalline CdZnTe film, which forms a photoconductive Au/graphene/CdZnTe/FTO structure. XRD, Raman, photoelectric response and other characterisation methods are adopted to investigate the effect of graphene layer on the electrical characteristics and UV photo-response performance of CdZnTe photoconductive structure. It is demonstrated that graphene layer can significantly improve the contact property of Au/CdZnTe structure, and obviously enhance its UV photo-response and the UV sensitivity increased with one order of magnitude.

Precious metal-bearing epithermal deposits in western Patagonia (NE Lago Fontana region), Argentina

Science.gov (United States)

Lanfranchini, Mabel Elena; Etcheverry, Ricardo Oscar; de Barrio, Raúl Ernesto; Recio Hernández, Clemente

2013-04-01

Precious metal-bearing quartz veins occur at the northeastern sector of the Lago Fontana region in southwestern Argentina, within the context of the Andean continental magmatic arc environment. The deposits and their associated alteration zones are spatially related to a Cretaceous calc-alkaline magmatism represented by silicic dikes and hypabyssal intrusions, and hosted by a Late Jurassic to Cretaceous volcano-sedimentary sequence. The veins and related veinlets crop out discontinuously, in general terms in a NW-SE belt. The primary vein mineral assemblage is composed mostly of pyrite ± galena ± chalcopyrite > hematite ± arsenopyrite in silica gangue minerals. Chemical analyses of grab samples from selected quartz veins show as much as 5.7 ppm Au and 224 ppm Ag, as well as elevated Pb, Cu, and Zn. Hydrothermal fluids caused an innermost silicification and adularia-sericite alteration assemblage, and an external propylitic halo. Sulfur isotope values measured for sulfides (δSS from -1.90 to +1.56‰), and oxygen and hydrogen isotopes measured on quartz crystals and extracted primary fluid inclusion waters (δOO = -2.85 to +5.40‰; δDO = -106.0 to -103.4‰) indicate that mineralization probably formed from magmatic fluids, which were mixed with meteoric waters. Also, fluid inclusion data from quartz veins point out that these fluids had low salinity (1.7-4.2 wt% NaCl equiv.), and temperatures of homogenization between 180 and 325 °C. Mineralogical, petrographic and geochemical features for mineralized surface exposures indicate a typical adularia-sericite, low sulfidation epithermal system in the Lago Fontana area that represents a promising target for further exploration programs.

Diffusion and aggrigation of implanted Ag and Au in a lithia-alumina-silica glass

International Nuclear Information System (INIS)

Arnold, G.W.; Borders, J.A.

1976-01-01

Optical extinction and Rutherford backscattering (RBS) techniques have been employed to obtain information on the size and spatial distribution of Au and Ag colloids in implanted (Au + ,Ag + )lithia-alumina-silica glass. The formation of metallic aggregates (colloids), necessary for preparation of a glass-ceramic surface layer, proceeds readily with annealing temperature for Au-implanted samples but not for Ag-implanted material. The optical and RBS spectra show that the particle size and spatial distribution in Ag-implanted samples are sensitive to sample temperature and ion-beam heating effects, while these parameters for Au-implanted samples are relatively insensitive to temperature and beam current. It is suggested that this behaviour is related to differences in the dissolution energies of Ag and Au aggregates. A two-peaked spatial distribution for Ag implanted at room temperature at a dose rate of approximately 1 μA cm -2 is observed which may result from the trappings of Ag in the ion displacement damage region of the glass during implantation. (author)

Surface tension estimation of high temperature melts of the binary alloys Ag-Au

Science.gov (United States)

Dogan, Ali; Arslan, Hüseyin

2017-11-01

Surface tension calculation of the binary alloys Ag-Au at the temperature of 1381 K, where Ag and Au have similar electronic structures and their atomic radii are comparable, are carried out in this study using several equations over entire composition range of Au. Apparently, the deviations from ideality of the bulk solutions, such as activities of Ag and Au are small and the maximum excess Gibbs free energy of mixing of the liquid phase is for instance -4500 J/mol at XAu = 0.5. Besides, the results obtained in Ag-Au alloys that at a constant temperature the surface tension increases with increasing composition while the surface tension decreases as the temperature increases for entire composition range of Au. Although data about surface tension of the Ag-Au alloy are limited, it was possible to make a comparison for the calculated results for the surface tension in this study with the available experimental data. Taken together, the average standard error analysis that especially the improved Guggenheim model in the other models gives the best agreement along with the experimental results at temperature 1383 K although almost all models are mutually in agreement with the other one.

The Role of Work Function and Band Gap in Resistive Switching Behaviour of ZnTe Thin Films

Science.gov (United States)

Rowtu, Srinu; Sangani, L. D. Varma; Krishna, M. Ghanashyam

2018-02-01

Resistive switching behavior by engineering the electrode work function and band gap of ZnTe thin films is demonstrated. The device structures Au/ZnTe/Au, Au/ZnTe/Ag, Al/ZnTe/Ag and Pt/ZnTe/Ag were fabricated. ZnTe was deposited by thermal evaporation and the stoichiometry and band gap were controlled by varying the source-substrate distance. Band gap could be varied between 1.0 eV to approximately 4.0 eV with the larger band gap being attributed to the partial oxidation of ZnTe. The transport characteristics reveal that the low-resistance state is ohmic in nature which makes a transition to Poole-Frenkel defect-mediated conductivity in the high-resistance states. The highest R off-to- R on ratio achieved is 109. Interestingly, depending on stoichiometry, both unipolar and bipolar switching can be realized.

Facile synthesis of PdAgTe nanowires with superior electrocatalytic activity

Science.gov (United States)

Hong, Wei; Wang, Jin; Wang, Erkang

2014-12-01

In this work, ultrathin Te nanowires (NWs) with high-aspect-ratio are prepared by a simple hydrothermal method. By using Te NWs as the sacrificial template, we demonstrate a facile and efficient method for the synthesis of PdAgTe NWs with high-quality through the partly galvanic replacement between Te NWs and the corresponding noble metal salts precursors in an aqueous solution. The compositions of PdAgTe NWs can be tuned by simply altering the concentration of the precursors. After cyclic voltammetry treatment, multi-component PdAgTe NW with a highly active and stable surface can be obtained. The structure and composition of the as-prepared nanomaterials are analyzed by transmission electron microscope, X-ray diffraction, energy dispersive X-ray spectroscopy, inductively coupled plasma-mass spectroscopy and X-ray photoelectron spectroscopy. Electrochemical catalytic measurement results prove that the as synthesized PdAgTe NWs present superior catalytic activity toward ethanol electrooxidation in alkaline solution than the commercial Pd/C catalyst, which making them can be used as effective catalysts for the direct ethanol fuel cells.

SERS-active Ag, Au and Ag–Au alloy nanoparticles obtained by laser ablation in liquids for sensing methylene blue

Energy Technology Data Exchange (ETDEWEB)

Olea-Mejía, Oscar, E-mail: oleaoscar@yahoo.com.mx [Centro Conjunto de Investigación en Química Sustentable UAEM-UNAM, Universidad Autónoma del Estado de México, km 14.5 Carretera Toluca-Atlacomulco, San Cayetano 50200, México (Mexico); Fernández-Mondragón, Mariana; Rodríguez-de la Concha, Gabriela [Centro Conjunto de Investigación en Química Sustentable UAEM-UNAM, Universidad Autónoma del Estado de México, km 14.5 Carretera Toluca-Atlacomulco, San Cayetano 50200, México (Mexico); Camacho-López, Marco [Laboratorio de Investigación y Desarrollo de Materiales Avanzados, Universidad Autónoma del Estado de México, Km 14.5 Carretera Toluca-Atlacomulco, San Cayetano 50925, México (Mexico)

2015-09-01

Highlights: • We synthesized Ag/Au nanoparticles by laser ablation in liquids. • We characterized such particles by UV–vis, TEM and EDS/STEM. • The SERS effect was studied for the obtained nanoparticles. • Pure silver nanoparticles showed the highest SERS signals. • We can sense methylene blue at a concentration of 10{sup −10} mole/L. - Abstract: We have synthesized Ag–Au nanoparticles by laser ablation in liquids using five different targets: 100% Ag, 80%Ag/20%Au, 50%Ag/50%Au, 20%Ag/80%Au and 100% Au (weight percentages). We used ethanol and methylene blue solutions in ethanol as the liquid media. The nanoparticles were mostly spherical with diameters 15, 19, 18, 23 and 11 nm, respectively. When alloyed targets were used, the resulting nanoparticles were completely alloyed forming solid solutions as evidenced by UV–vis Spectroscopy and Scanning Transmission Electron Microscopy. The obtained nanoparticles were employed to study the SERS effect of the methylene blue molecule. All the samples showed good SERS activity, however the ones composed of pure silver showed the greatest Raman signal enhancement. Finally, pure Ag nanoparticles were used for sensing methylene blue at different concentrations. While almost no signal can be discerned from the Raman spectrum when no particles are used at a concentration of methylene blue of 1 × 10{sup −2} M (∼3000 ppm), when Ag nanoparticles are used one can observe the characteristic peak of the molecule at concentrations as low as 1 × 10{sup −10} M (∼3 × 10{sup −5} ppm)

Study of Ag and Au Nanoparticles Synthesized by Arc Discharge in Deionized Water

Directory of Open Access Journals (Sweden)

Der-Chi Tien

2010-01-01

Full Text Available The paper presents a study of Ag and Au nanofluids synthesized by the arc discharge method (ADM in deionized water. The metallic Ag nanoparticle (Ag0 and ionic Ag (Ag+ have played an important role in the battle against germs which are becoming more drug-resistant every year. Our study indicates that Ag nanoparticle suspension (SNPS fabricated by using ADM without added surfactants exclusively contains the metallic Ag nanoparticle and ionic Ag. Besides that, the ADM in deionized water has also been employed for the fabrication process of Au nanoparticles. The experimental results indicate that the prepared Ag nanoparticles can react with the dissolved H2CO3 in deionized water, leading to the formation of Ag2CO3. Significantly different to Ag, the prepared Au nanoparticles with their surfaces bonded by oxygen are suspended in deionized water by the formation of hydrogen bonded with the neighboring water molecules.

Templated Atom-Precise Galvanic Synthesis and Structure Elucidation of a [Ag 24 Au(SR) 18 ] − Nanocluster

KAUST Repository

Bootharaju, Megalamane Siddaramappa

2015-11-27

Synthesis of atom-precise alloy nanoclusters with uniform composition is challenging when the alloying atoms are similar in size (for example, Ag and Au). A galvanic exchange strategy has been devised to produce a compositionally uniform [Ag24Au(SR)18]- cluster (SR: thiolate) using a pure [Ag25(SR)18]- cluster as a template. Conversely, the direct synthesis of Ag24Au cluster leads to a mixture of [Ag25-xAux(SR)18]-, x=1-8. Mass spectrometry and crystallography of [Ag24Au(SR)18]- reveal the presence of the Au heteroatom at the Ag25 center, forming Ag24Au. The successful exchange of the central Ag of Ag25 with Au causes perturbations in the Ag25 crystal structure, which are reflected in the absorption, luminescence, and ambient stability of the particle. These properties are compared with those of Ag25 and Ag24Pd clusters with same ligand and structural framework, providing new insights into the modulation of cluster properties with dopants at the single-atom level.

Precipitation hardening of a Cu-free Au-Ag-Pd-In dental alloy

Energy Technology Data Exchange (ETDEWEB)

Seol, Hyo-Joung [Department of Dental Materials, College of Dentistry and Research Institute for Oral Biotechnology, Pusan National University, 1-10 Ami-dong, Seo-gu, Pusan 602-739 (Korea, Republic of); Son, Kuk-Hyeon [Department of Dental Materials, College of Dentistry and Research Institute for Oral Biotechnology, Pusan National University, 1-10 Ami-dong, Seo-gu, Pusan 602-739 (Korea, Republic of); Yu, Chin-Ho [Department of Dental Materials, College of Dentistry and Research Institute for Oral Biotechnology, Pusan National University, 1-10 Ami-dong, Seo-gu, Pusan 602-739 (Korea, Republic of); Kwon, Yong Hoon [Department of Dental Materials, College of Dentistry and Research Institute for Oral Biotechnology, Pusan National University, 1-10 Ami-dong, Seo-gu, Pusan 602-739 (Korea, Republic of); Kim, Hyung-Il [Department of Dental Materials, College of Dentistry and Research Institute for Oral Biotechnology, Pusan National University, 1-10 Ami-dong, Seo-gu, Pusan 602-739 (Korea, Republic of)]. E-mail: hilkim@pusan.ac.kr

2005-10-27

The hardening mechanism and related microstructural changes of the Cu-free dental casting alloy composed of Au-Ag-Pd-In was examined by means of hardness test, X-ray diffraction (XRD), scanning electron microscopic (SEM) observations and electron probe microanalysis (EPMA). The Au-Ag-Pd-In alloy showed apparent age-hardenability. In the SEM photograph, three phases were observed in the solution-treated specimen, that is, the Au-Ag based phase with small amounts of In and Pd as matrix, the InPd phase as particle-like structures, and the Pd-rich phase as lamellar precipitates. By aging the specimen, the very fine Pd-rich inter-granular precipitates grew toward the grain interior as lamellar structure, and finally the coarsened Pd-rich precipitates covered a large part of the Au-Ag based matrix. The hardness increase in the early stage of the age-hardening process was assumed to be caused by the diffusion and aggregation of Pd atoms from the Au-Ag based matrix. The hardness decrease in the later stage of age-hardening process was caused by coarsening of the lamellar precipitates composed of the Pd-rich phase.

Precipitation hardening of a Cu-free Au-Ag-Pd-In dental alloy

International Nuclear Information System (INIS)

Seol, Hyo-Joung; Son, Kuk-Hyeon; Yu, Chin-Ho; Kwon, Yong Hoon; Kim, Hyung-Il

2005-01-01

The hardening mechanism and related microstructural changes of the Cu-free dental casting alloy composed of Au-Ag-Pd-In was examined by means of hardness test, X-ray diffraction (XRD), scanning electron microscopic (SEM) observations and electron probe microanalysis (EPMA). The Au-Ag-Pd-In alloy showed apparent age-hardenability. In the SEM photograph, three phases were observed in the solution-treated specimen, that is, the Au-Ag based phase with small amounts of In and Pd as matrix, the InPd phase as particle-like structures, and the Pd-rich phase as lamellar precipitates. By aging the specimen, the very fine Pd-rich inter-granular precipitates grew toward the grain interior as lamellar structure, and finally the coarsened Pd-rich precipitates covered a large part of the Au-Ag based matrix. The hardness increase in the early stage of the age-hardening process was assumed to be caused by the diffusion and aggregation of Pd atoms from the Au-Ag based matrix. The hardness decrease in the later stage of age-hardening process was caused by coarsening of the lamellar precipitates composed of the Pd-rich phase

Diffusion and aggregation of implanted Ag and Au in a lithia--alumina--silica glass

International Nuclear Information System (INIS)

Arnold, G.W.; Borders, J.A.

1975-01-01

Optical extinction and Rutherford backscattering (RBS) techniques were employed to obtain information on the size and spatial distribution of Au- and Ag-colloids in implanted (Au + , Ag + ) lithia-alumina-silica glass. The formation of metallic aggregates (colloids), necessary for preparation of a glass-ceramic surface layer, proceeds readily with annealing temperature for Au-implanted samples but not for Ag-implanted material. The optical and RBS spectra show that the particle size and spatial distribution in as-implanted samples are sensitive to sample temperature and ion-beam heating effects, while these parameters for Au-implanted samples are relatively insensitive to temperature and beam current. It is suggested that this behavior is related to differences in the dissolution energies of Ag and Au aggregates. A two-peaked spatial distribution for Ag implanted at room temperature at a dose rate of approximately 1 μA/cm 2 is observed which may result from the trapping of Ag in the compacted damage region of the glass during implantation. (auth)

Defect complexes formed with Ag atoms in CDTE, ZnTe, and ZnSe

CERN Document Server

Wolf, H; Ostheimer, V; Hamann, J; Lany, S; Wichert, T

2000-01-01

Using the radioactive acceptor $^{111}\\!$Ag for perturbed $\\gamma$-$\\gamma$-angular correlation (PAC) spectroscopy for the first time, defect complexes formed with Ag are investigated in the II-VI semiconductors CdTe, ZnTe and ZnSe. The donors In, Br and the Te-vacancy were found to passivate Ag acceptors in CdTe via pair formation, which was also observed in In-doped ZnTe. In undoped or Sb-doped CdTe and in undoped ZnSe, the PAC experiments indicate the compensation of Ag acceptors by the formation of double broken bond centres, which are characterised by an electric field gradient with an asymmetry parameter close to h = 1. Additionally, a very large electric field gradient was observed in CdTe, which is possibly connected with residual impurities.

Self-standing corrugated Ag and Au-nanorods for plasmonic applications

DEFF Research Database (Denmark)

Habouti, S.; Mátéfi-Tempfli, M.; Solterbeck, C.-H.

2011-01-01

We use home-made Si-supported anodized alumina thin film templates for the electrodeposition of large area self-standing Ag- and Au-nanorod (Au-NR) arrays. The deposition conditions chosen, i.e. electrolyte composition and deposition voltage, lead to a corrugated rod morphology, particularly for Au...

Physical Properties Of Some Pd-Au-Ag Ternary Alloys: A Md Study

International Nuclear Information System (INIS)

Aydin, G.

2010-01-01

Mechanical properties of palladium (Pd), gold (Au) and silver (Ag) and their ternary alloys in the following concentrations (Au 5 0Ag 2 5Pd 2 5, Au 4 0Ag 2 0Pd 4 0) are studied by using by using molecular dynamics with Quantum Sutton-Chen (Q-SC) potential. Cell constants, densities, enthalpies, elastic constants and heat capacities are investigated. Calculations are performed in the solid phase. Rafii-Tabar combination rules are used and it is showed that these combination rules are valid for ternary alloys also. Additionally, temperature dependence of mechanical properties of alloys are investigated.

Production of φ mesons in Au-Au collisions at the AGS

International Nuclear Information System (INIS)

Back, B. B.; Betts, R. R.; Chang, J.; Gillitzer, A.; Henning, W. F.; Hofman, D. J.; Nanal, V.; Seto, R.; Wuosmaa, A. H.; Xiang, H.

1999-01-01

The first measurements of φ meson production in Au-Au collisions at AGS energies are presented via the decay to K + K - . A measurement of the centrality dependence of the yield shows an increase similar to that seen for the K - with a spectral shape consistent with a relativistic Breit-Wigner distribution within the statistical errors of the present data set. Future analysis using the full data set with 4 times the statistics will allow a more accurate determination of the yields, slopes and spectral shapes

An SFG and DFG investigation of polycrystalline Au, Au-Cu and Au-Ag-Cu electrodes in contact with aqueous solutions containing KCN

International Nuclear Information System (INIS)

Bozzini, Benedetto; Busson, Bertrand; De Gaudenzi, Gian Pietro; Mele, Claudio; Tadjeddine, Abderrahmane

2007-01-01

In this paper, the behaviour of polycrystalline Au, Au-Cu (Cu 25%) and Au-Ag-Cu (Ag 10%, Cu 15%) electrodes in contact with neutral aqueous solutions of KCN has been studied as a function of potential by means of in situ sum frequency generation (SFG) and difference frequency generation (DFG) spectroscopies. The potential-dependent spectra have been analysed quantitatively with a model for the second-order non-linear susceptibility accounting for vibrational and electronic effects. The potential-dependence of the CN - stretching band position and of the free-electron contribution to the real part of the non-resonant component of the second-order susceptibility have been accounted for. Spectroelectrochemical results were complemented by cyclic voltammetric measurements. The chief stress in this work has been placed on systematising and quantifying the interaction between the vibrational and electronic structures of the electrodic interfaces studied. The effects of adsorbates on the electronic structure of the adsorbing electrode, as a function of electrode alloy composition and applied potential are particularly critical for the understanding of Au-alloy electrochemistry in the presence of cyanide and cyanocomplexes. The systematic comparison of SFG and DFG spectra measured under the same electrochemical conditions for Au, Au-Cu and Au-Ag-Cu electrodes discloses a rich phenomenology related to the electronic structure of the interface

An SFG and DFG investigation of polycrystalline Au, Au-Cu and Au-Ag-Cu electrodes in contact with aqueous solutions containing KCN

Energy Technology Data Exchange (ETDEWEB)

Bozzini, Benedetto [Dipartimento di Ingegneria dell' Innovazione, Universita di Lecce, v. Monteroni, I-73100 Lecce (Italy)]. E-mail: benedetto.bozzini@unile.it; Busson, Bertrand [CLIO-LCP, Universite Paris-Sud, 91405 Orsay Cedex (France); De Gaudenzi, Gian Pietro [Dipartimento di Ingegneria dell' Innovazione, Universita di Lecce, v. Monteroni, I-73100 Lecce (Italy); Mele, Claudio [Dipartimento di Ingegneria dell' Innovazione, Universita di Lecce, v. Monteroni, I-73100 Lecce (Italy); Tadjeddine, Abderrahmane [UDIL-CNRS, Bat. 201, Centre Universitaire Paris-Sud, BP 34, 91898 Orsay Cedex (France)

2007-01-16

In this paper, the behaviour of polycrystalline Au, Au-Cu (Cu 25%) and Au-Ag-Cu (Ag 10%, Cu 15%) electrodes in contact with neutral aqueous solutions of KCN has been studied as a function of potential by means of in situ sum frequency generation (SFG) and difference frequency generation (DFG) spectroscopies. The potential-dependent spectra have been analysed quantitatively with a model for the second-order non-linear susceptibility accounting for vibrational and electronic effects. The potential-dependence of the CN{sup -} stretching band position and of the free-electron contribution to the real part of the non-resonant component of the second-order susceptibility have been accounted for. Spectroelectrochemical results were complemented by cyclic voltammetric measurements. The chief stress in this work has been placed on systematising and quantifying the interaction between the vibrational and electronic structures of the electrodic interfaces studied. The effects of adsorbates on the electronic structure of the adsorbing electrode, as a function of electrode alloy composition and applied potential are particularly critical for the understanding of Au-alloy electrochemistry in the presence of cyanide and cyanocomplexes. The systematic comparison of SFG and DFG spectra measured under the same electrochemical conditions for Au, Au-Cu and Au-Ag-Cu electrodes discloses a rich phenomenology related to the electronic structure of the interface.

Deformation of Ag clusters deposited on Au(111) - Experiment and molecular dynamics

Energy Technology Data Exchange (ETDEWEB)

Miroslawski, Natalie; Groenhagen, Niklas; Hoevel, Heinz [TU Dortmund, Experimentelle Physik I (Germany); Issendorff, Bernd von [Universitaet Freiburg, Fakultaet Physik (Germany); Jaervi, Tommi [Fraunhofer Institut fuer Werkstoffmechanik, Freiburg (Germany); Moseler, Michael [Universitaet Freiburg, Fakultaet Physik (Germany); Fraunhofer Institut fuer Werkstoffmechanik, Freiburg (Germany); Freiburger Materialforschungszentrum (Germany)

2011-07-01

Mass selected clusters from Ag{sup +}{sub 55} to Ag{sup +}{sub 147{+-}}{sub 2} were deposited with different deposition energies at 77 K on Au(111) and imaged with STM at 77 K. We observed a deformation of the cluster shape due to the strong metallic interaction between the cluster and the substrate. The clusters became epitaxial and developed a structure composed of several Ag monolayers. The number of these monolayers depends on the number of atoms in the cluster and the deposition energy. The larger the cluster mass the more monolayers the cluster develops on Au(111) and the larger the deposition energy the fewer monolayers occur. These results were verified by molecular dynamic simulations. Additionally the behaviour of Ag{sub N} clusters on Au(111) after different annealing steps was investigated.

Anchoring of Ag-Au alloy nanoparticles on reduced graphene oxide sheets for the reduction of 4-nitrophenol

Energy Technology Data Exchange (ETDEWEB)

Hareesh, K., E-mail: appi.2907@gmail.com [Department of Physics, Savitribai Phule Pune University, Pune 411007 (India); Joshi, R.P. [Department of Physics, Savitribai Phule Pune University, Pune 411007 (India); Sunitha, D.V. [School of Physics, Reva University, Bangalore 560064 (India); Bhoraskar, V.N. [Department of Physics, Savitribai Phule Pune University, Pune 411007 (India); Dhole, S.D., E-mail: sanjay@physics.unipune.ac.in [Department of Physics, Savitribai Phule Pune University, Pune 411007 (India)

2016-12-15

Highlights: • Ag-Au-rGO nanocomposite was synthesized by gamma radiation assisted method. • Ag-Au nanoparticles of size (5–19) nm were decorated on rGO. • Ag-Au-rGO showed enhanced catalytic activity for reduction of 4-Nitrophenol. - Abstract: One-step gamma radiation assisted method has been used for the synthesis of Silver-Gold (Ag-Au) alloy nanoparticles with simultaneous reduction of graphene oxide (GO). UV–vis spectroscopic results along with X-ray diffraction analysis, X-ray Photoelectron spectroscopy and Transmission electron microscopy confirmed the decoration face centered cubic structured Ag-Au nanoparticles of size (5–19) nm on reduced graphene oxide (rGO) sheets. The increase in disorder parameter in Raman spectroscopy indicates the formation of more number of small sp{sup 2} domains. The synthesized Ag-Au-rGO nanocomposite showed enhanced catalytic activity towards the reduction of 4-Nitrophenol compared to individual Ag-Au and rGO components.

Effect of laser irradiation on Ag4In12Sb56Te28

Science.gov (United States)

Chinnusamy, Rangasami

2018-04-01

Ag4In12Sb56Te28 has been synthesized by melt-quench method. Phase homogeneity, crystal structure and effect of laser irradiation have been investigated using X-ray diffraction (XRD) and Raman spectroscopy. Rietveld refinement of crystal structure revealed that Ag4In12Sb56Te28 is a multiphase system with AgIn3Te5, Sb8Te3 and Sb phases. Combined optical microscopy and Raman spectroscopy have been used to understand the distribution of different phases on the surface of the samples, which substantiated the results of Rietveld analysis. Interaction of 20 mW laser beam with samples has been investigated using Raman measurements. The results have shown that regions with large phase fraction of AgIn3Te5 become amorphous during laser-sample interaction, but the starting phase remains nearly same after the interaction. Regions with AgIn3Te5 and nearly equal or larger amount of Sb8Te3 have shown significant growth of α-Sb2O3 during and after laser-sample interaction. Regions rich in Sb have shown formation of AgIn3Te5 and growth of α-Sb2O3 during and after interaction. These observations have been explained based on the maximum temperature rise at different regions during laser-sample interaction.

Development of Au-Ag nanowire mesh fabrication by UV-induced approach

Energy Technology Data Exchange (ETDEWEB)

Saggar, Siddhartha [Laboratory for Molecular Photonics and Electronics, Department of Physics, National Institute of Technology, Calicut, Kerala, India and School of Nanoscience and Technology, National Institute of Technology, Calicut, Kerala (India); Predeep, Padmanabhan, E-mail: predeep@nitc.ac.in

2014-10-15

In an attempt to overcome the limitations of the presently prevailing transparent conducting electrode (TCE) - indium tin oxide (ITO) - many materials have been considered for replacing ITO. Recently, a novel method has been reported for the synthesis of Au-Ag nanowire (NW) mesh, and tested successfully for organic-light-emitting-diodes (OLEDs). It employs UV-induced reduction of gold- and silver- precursors to form Au-Ag NW mesh. In this report, Au-Ag NW mesh thin films are synthesized on glass substrates with an objective for use as facing-electrode for Organic Photovoltaics. Various issues and factors affecting the fabrication-process have been improved, and are also discussed here. The electrode showed good transmitivity, of around 95% (excluding that of glass substrate). The advantage of the technique is its simple processing method and cost-effectiveness.

Alloy formation during the electrochemical growth of a Ag-Cd ultrathin film on Au(1 1 1)

International Nuclear Information System (INIS)

Barrio, M.C. del; Garcia, S.G.; Salinas, D.R.

2009-01-01

The electrodeposition of a Ag/Cd ultrathin film on a Au(1 1 1) surface and the formation of a surface alloy during this process have been studied using classical electrochemical techniques and in situ Scanning Tunneling Microscopy (STM). The films were obtained from separate electrolytes containing Ag + or Cd 2+ ions and from a multicomponent solution containing both ions. First, the polarization conditions were adjusted in order to form a Ag film by overpotential deposition. Afterwards, a Cd monolayer was formed onto this Au(1 1 1)/Ag modified surface by underpotential deposition. The voltammetric behavior of the Cd UPD and the in situ STM images indicated that the ultrathin Ag films were uniformly deposited and epitaxially oriented with respect to the Au(1 1 1) surface. Long time polarization experiments showed that a significant Ag-Cd surface alloying accompanied the formation of the Cd monolayer on the Au(1 1 1)/Ag modified surface, independent of the Ag film thickness. In the case of an extremely thin Ag layer (1 Ag ML) the STM images and long time polarization experiments revealed a solid state diffusion process of Cd, Ag, and Au atoms which can be responsible for the formation of different Ag-Cd or Au-Ag-Cd alloy phases.

Au@Ag core-shell nanocubes with finely tuned and well-controlled sizes, shell thicknesses, and optical properties.

Science.gov (United States)

Ma, Yanyun; Li, Weiyang; Cho, Eun Chul; Li, Zhiyuan; Yu, Taekyung; Zeng, Jie; Xie, Zhaoxiong; Xia, Younan

2010-11-23

This paper describes a facile method for generating Au@Ag core-shell nanocubes with edge lengths controllable in the range of 13.4-50 nm. The synthesis involved the use of single-crystal, spherical Au nanocrystals of 11 nm in size as the seeds in an aqueous system, with ascorbic acid serving as the reductant and cetyltrimethylammonium chloride (CTAC) as the capping agent. The thickness of the Ag shells could be finely tuned from 1.2 to 20 nm by varying the ratio of AgNO(3) precursor to Au seeds. We also investigated the growth mechanism by examining the effects of seeds (capped by CTAC or cetyltrimethylammonium bromide(CTAB)) and capping agent (CTAC vs CTAB) on both size and shape of the resultant core-shell nanocrystals. Our results clearly indicate that CTAC worked much better than CTAB as a capping agent in both the syntheses of Au seeds and Au@Ag core-shell nanocubes. We further studied the localized surface plasmon resonance properties of the Au@Ag nanocubes as a function of the Ag shell thickness. By comparing with the extinction spectra obtained from theoretical calculations, we derived a critical value of ca. 3 nm for the shell thickness at which the plasmon excitation of the Au cores would be completely screened by the Ag shells. Moreover, these Au@Ag core-shell nanocubes could be converted into Au-based hollow nanostructures containing the original Au seeds in the interiors through a galvanic replacement reaction.

Synthesis and characterization of the ternary telluroargentate K4[Ag18Te11

KAUST Repository

Davaasuren, Bambar

2014-10-19

The ternary potassium telluroargentate(I), K4[Ag18Te11], was prepared by solvothermal synthesis in ethylenediamine at 160 °C. It crystallizes in the cubic space group Fm3¯ m (no. 225) with the cell parameter a = 18.6589(6) Å. The crystal structure can be described as a [Ag18Te11]4- three-dimensional anionic framework with the voids accommodating potassium cations. Chemical bonding analysis reveals polar covalent Ag-Te bonds and considerable Ag-Ag interactions, which support the complex anionic character of the structure. The compound is thermally stable up to 450 °C in an inert atmosphere.

Geochemical Peculiarities of Galena and Sphalerite from Polymetallic Deposits of the Dal'negorskii Ore Region (Primorsky Krai, Russia)

Science.gov (United States)

Rogulina, L. I.; Moiseenko, V. G.; Ponomarchuk, V. A.

2018-04-01

New data on the composition of the major minerals from the skarn and vein polymetallic deposits of the Dal'negorskii ore region are reported. Analysis of galena and sphalerite was carried out by the X-ray fluorescent energy-dispersive method of synchrotron radiation for the first time. It is shown that the minor elements in major minerals of different deposits are typomorphic. Among these elements are Fe, Cu, Ni, Cd, Ag, Sn, and Sb, as well as In in sphalerite and Te in galena. The high concentrations of Ag, Cu, Te, Cd, and In in the extracted minerals indicate the complex character of mineralization. The compositional patterns of ore minerals characterize the sequence of mineral formation from the skarn to vein ores, and the sequence of deposits from the mesothermal to epithermal conditions. This provides geochemical evidence for the stage model of the formation of mineralization in the Dal'negorskii ore region.

An Atomically Precise Au10 Ag2 Nanocluster with Red-Near-IR Dual Emission.

Science.gov (United States)

Lei, Zhen; Guan, Zong-Jie; Pei, Xiao-Li; Yuan, Shang-Fu; Wan, Xian-Kai; Zhang, Jin-Yuan; Wang, Quan-Ming

2016-08-01

A red-near-IR dual-emissive nanocluster with the composition [Au10 Ag2 (2-py-C≡C)3 (dppy)6 ](BF4 )5 (1; 2-py-C≡C is 2-pyridylethynyl, dppy=2-pyridyldiphenylphosphine) has been synthesized. Single-crystal X-ray structural analysis reveals that 1 has a trigonal bipyramidal Au10 Ag2 core that contains a planar Au4 (2-py-C≡C)3 unit sandwiched by two Au3 Ag(dppy)3 motifs. Cluster 1 shows intense red-NIR dual emission in solution. The visible emission originates from metal-to-ligand charge transfer (MLCT) from silver atoms to phosphine ligands in the Au3 Ag(dppy)3 motifs, and the intense NIR emission is associated with the participation of 2-pyridylethynyl in the frontier orbitals of the cluster, which is confirmed by a time-dependent density functional theory (TD-DFT) calculation. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Measurement of thermal, epithermal and fast neutrons fluxes by the activation foil method at IEA-R1 reactor

International Nuclear Information System (INIS)

Dias, M.S.; Koskinas, M.F.; Berretta, J.R.; Fratin, L.; Botelho, S.

1990-01-01

The thermal, epithermal and fast neutron fluxes have been determined experimentally by the activation foil method at position GI, located near the IEA-R1 reactor core. The reactions used were 197 Au (n,gamma) 198 Au, for thermal and epithermal neutrons and 27 Na (n,alpha) 24 Na, for fast neutrons. The activities were measured by the 4π(PC)β-γ coincidence method. (author)

Fabrication of Te@Au core-shell hybrids for efficient ethanol oxidation

Science.gov (United States)

Jin, Huile; Wang, Demeng; Zhao, Yuewu; Zhou, Huan; Wang, Shun; Wang, Jichang

2012-10-01

Using Au nanoparticles to catalyze the oxidation of alcohols has garnered increasing attention due to its potential application in direct alcohol fuel cells. In this research Te@Au core-shell hybrids were fabricated for the catalytic oxidation of ethanol, where the preparation procedure involved the initial production of Te crystals with different microstructures and the subsequent utilization of the Te crystal as a template and reducing agent for the production of Te@Au hybrids. The as-prepared core-shell hybrids were characterized by scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy, and X-ray diffraction techniques. Electrochemical measurements illustrate that the hybrids have great electrocatalytic activity and stability toward ethanol oxidation in alkaline media. The enhanced electrocatalytic property may be attributed to the cooperative effects between the metal and semiconductor and the presence of a large number of active sites on the hybrids surface.

Typomorphic Characteristics of Molybdenite from the Bystrinsky Cu-Au Porphyry-Skarn Deposit, Eastern Transbaikal Region, Russia

Science.gov (United States)

Kovalenker, V. A.; Trubkin, N. V.; Abramova, V. D.; Plotinskaya, O. Yu.; Kiseleva, G. D.; Borisovskii, S. E.; Yazykova, Yu. I.

2018-01-01

The paper presents pioneering data on the composition, texture, and crystal structure of molybdenite from various types of molybdenum mineralization at the Bystrinsky Cu-Au-Fe porphyry-skarn deposit in the eastern Transbaikal region, Russia. The data were obtained using electron microprobe analysis (EMPA), laser ablation-inductively coupled plasma mass spectrometry (LA-ICP-MS), and high-resolution transmission electron microscopy (HRTEM). Molybdenite found at the deposit in skarn, sulfide-poor quartz veins, and quartz-feldspar alteration markedly differs in the concentrations of trace elements determined by their species in the mineral, as well as in its structural features. Molybdenite-2H from skarn associated with phyllosilicates occurs as ultrafine crystals with uniform shape and texture; no dislocations or inclusions were found but amorphous silica was. The molybdenite composition is highly contrasting in the content and distribution of both structure-related (Re, W, and Se) and other (Mn, Co, Ni, Cu, Zn, As, Ag, Cd, Sb, Te, Ag, Pd, Au, Hg, Pb, and Bi) metals. In the sulfide-poor quartz veins, highly structurally heterogeneous (2H + 3R) molybdenite microcrystals with abundant defects (dislocations and volumetrically distributed inclusions) are associated with illite, goethite, and barite. Some single crystals are unique three-phase (2H + 3R polytypes + amorphous MoS2). The mineral has a low concentration of all trace elements, which are uniformly distributed. However, individual domains with uniquely high Pd, Te, Ni, Hg, and W concentrations caused by mineral inclusions are found in some grains. Molybdenite from quartz-feldspar alteration is characterized by low concentrations of all trace elements except for Re and Se, which enrich some domains of the grains. Our data indicate that the compositional and structural heterogeneity of molybdenite from the Bystrinsky deposit are its crucial features, which obviously correlate with the types of Mo mineralization.

Enzyme-free hydrogen peroxide sensor based on Au@Ag@C core-double shell nanocomposites

Energy Technology Data Exchange (ETDEWEB)

Li, Yancai, E-mail: liyancai@mnnu.edu.cn [College of Chemistry & Environment, Minnan Normal University, Zhangzhou 363000 (China); Fujian Province Key Laboratory of Modern Analytical Science and Separation Technology, Minnan Normal University, Zhangzhou 363000 (China); Zhang, Yayun; Zhong, Yanmei [College of Chemistry & Environment, Minnan Normal University, Zhangzhou 363000 (China); Li, Shunxing [College of Chemistry & Environment, Minnan Normal University, Zhangzhou 363000 (China); Fujian Province Key Laboratory of Modern Analytical Science and Separation Technology, Minnan Normal University, Zhangzhou 363000 (China)

2015-08-30

Graphical abstract: - Highlights: • A facile method was designed to synthesize Au@Ag@C core-double shell nanocomposites. • Carbon nanomaterials at the outermost layer could protect Au and Ag nanoparticles from oxidation and aggregation. • The Au@Ag@C core-double shell nanocomposites showed high sensitivity and selectivity to electrocatalytic reduction of hydrogen peroxide. • The hydrogen peroxide sensor has a wide linear range of 5.0 μM to 4.75 mM and a limit of detection as low as 0.14 μM. - Abstract: The well-designed Au@Ag@C core-double shell nanocomposites were synthesized via a facile method, and were used to fabricate an enzyme-free amperometric hydrogen peroxide (H{sub 2}O{sub 2}) sensor. The size, shape, elementary composition and structure of the nanocomposites were characterized by transmission electron microscope (TEM), energy-dispersed spectrum (EDS) and X-ray diffraction (XRD). The outermost layer of the nanocomposites was amorphous carbon, the second layer was Ag and the core was Au. The Au@Ag@C core-double shell nanocomposites exhibit attractive activity for electrocatalytic reduction of H{sub 2}O{sub 2} according to the electrochemical experiments. It also demonstrates the H{sub 2}O{sub 2} sensor possess well performance with a wide linear range of 5.0 μM to 4.75 mM and a limit of detection (LOD) as low as 0.14 μM (S/N = 3). Furthermore, the interference from the common interfering species, such as glucose, ascorbic acid, dopamine and uric acid can be effectively avoided. In a word, the Au@Ag@C nanocomposites are promising candidates for enzyme-free H{sub 2}O{sub 2} sensor.

Studying the Range of Incident Alpha Particles on Cu , Ge , Ag , Cd , Te and Au, With Energy (4-15 MeV)

International Nuclear Information System (INIS)

Kadhim, R.O.; Jasim, W.N.

2015-01-01

In this paper theoretical calculation of the range for alpha particles with the energy range (4 – 15)MeV when passing in some metallic media (Cu , Ge , Ag , Cd , Te and Au).Semi empirical formula was used in addition to (SRIM-2012) program. The Semi empirical equation was programmed to calculate the range using Matlab Language.The results of the range in these media were compared with the results obtained from SRIM-2012 and )(2011)Andnet) results.There was good agreement among the semi empirical equation result , SRIM- 2012 results and with )(2011)Andnet) results in the low energy.The results showed exponential relation between the range of alpha particles in these media and the velocity of the particles.By recourse with SRIM- 2012 results and application them in Matlab program and by using Curve Fitting Tool we extraction equation with its constants to calculate the range of alpha particles in any element of these six elements with the energy range (4 – 15)MeV.The maximum deviation between the results from the semi empirical calculation and SRIM-2012 results was calculated the statistical test ( kstest2) in Matlab program

Collagen-chitosan scaffold modified with Au and Ag nanoparticles: Synthesis and structure

International Nuclear Information System (INIS)

Rubina, M.S.; Kamitov, E.E.; Zubavichus, Ya. V.; Peters, G.S.; Naumkin, A.V.; Suzer, S.; Vasil’kov, A.Yu.

2016-01-01

Graphical abstract: - Highlights: • Biocompatible collagen-chitosan scaffolds were modified by Au and Ag nanoparticles via the metal-vapor synthesis. • Structural and morphological parameters of the nanocomposites were assessed using a set of modern instrumental techniques, including electron microscopy, X-ray diffraction, small-angle X-ray scattering, EXAFS, XPS. • Potential application of the nanocomposites are envisaged. - Abstract: Nowadays, the dermal biomimetic scaffolds are widely used in regenerative medicine. Collagen-chitosan scaffold one of these materials possesses antibacterial activity, good compatibility with living tissues and has been already used as a wound-healing material. In this article, collagen-chitosan scaffolds modified with Ag and Au nanoparticles have been synthesized using novel method - the metal-vapor synthesis. The nanocomposite materials are characterized by XPS, TEM, SEM and synchrotron radiation-based X-ray techniques. According to XRD data, the mean size of the nanoparticles (NPs) is 10.5 nm and 20.2 nm in Au-Collagen-Chitosan (Au-CollCh) and Ag-Collagen-Chitosan (Ag-CollCh) scaffolds, respectively in fair agreement with the TEM data. SAXS analysis of the composites reveals an asymmetric size distribution peaked at 10 nm for Au-CollCh and 25 nm for Ag-CollCh indicative of particle's aggregation. According to SEM data, the metal-carrying scaffolds have layered structure and the nanoparticles are rather uniformly distributed on the surface material. XPS data indicate that the metallic nanoparticles are in their unoxidized/neutral states and dominantly stabilized within the chitosan-rich domains.

Collagen-chitosan scaffold modified with Au and Ag nanoparticles: Synthesis and structure

Energy Technology Data Exchange (ETDEWEB)

Rubina, M.S.; Kamitov, E.E. [A.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Moscow, 119991 Russian Federation (Russian Federation); Zubavichus, Ya. V.; Peters, G.S. [National Research center «Kurchatov Institute», Moscow, 123182 Russian Federation (Russian Federation); Naumkin, A.V. [A.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Moscow, 119991 Russian Federation (Russian Federation); Suzer, S. [Department of Chemistry, Bilkent University, Ankara, 06800 Turkey (Turkey); Vasil’kov, A.Yu., E-mail: alexandervasilkov@yandex.ru [A.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Moscow, 119991 Russian Federation (Russian Federation)

2016-03-15

Graphical abstract: - Highlights: • Biocompatible collagen-chitosan scaffolds were modified by Au and Ag nanoparticles via the metal-vapor synthesis. • Structural and morphological parameters of the nanocomposites were assessed using a set of modern instrumental techniques, including electron microscopy, X-ray diffraction, small-angle X-ray scattering, EXAFS, XPS. • Potential application of the nanocomposites are envisaged. - Abstract: Nowadays, the dermal biomimetic scaffolds are widely used in regenerative medicine. Collagen-chitosan scaffold one of these materials possesses antibacterial activity, good compatibility with living tissues and has been already used as a wound-healing material. In this article, collagen-chitosan scaffolds modified with Ag and Au nanoparticles have been synthesized using novel method - the metal-vapor synthesis. The nanocomposite materials are characterized by XPS, TEM, SEM and synchrotron radiation-based X-ray techniques. According to XRD data, the mean size of the nanoparticles (NPs) is 10.5 nm and 20.2 nm in Au-Collagen-Chitosan (Au-CollCh) and Ag-Collagen-Chitosan (Ag-CollCh) scaffolds, respectively in fair agreement with the TEM data. SAXS analysis of the composites reveals an asymmetric size distribution peaked at 10 nm for Au-CollCh and 25 nm for Ag-CollCh indicative of particle's aggregation. According to SEM data, the metal-carrying scaffolds have layered structure and the nanoparticles are rather uniformly distributed on the surface material. XPS data indicate that the metallic nanoparticles are in their unoxidized/neutral states and dominantly stabilized within the chitosan-rich domains.

Synthesis, characterization of Ag-Au core-shell bimetal nanoparticles and its application for electrocatalytic oxidation/sensing of L-methionine

Energy Technology Data Exchange (ETDEWEB)

Murugavelu, M.; Karthikeyan, B., E-mail: bkarthi_au@yahoo.com

2017-01-01

The Ag-Au core-shell bimetal nanoparticles (BNPs) was prepared using chemical reduction method. The prepared Ag-Au core-shell BNPs were characterized by UV–Visible (UV–Vis) spectroscopy, field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), high resolution transmission electron microscopy (HR-TEM), X-ray diffraction (XRD), atomic force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS) pattern. These results showed the Ag-Au BNPs exhibited core-shell shape. The Ag-Au core-shell BNPs was examined towards electrocatalytic oxidation of L-methionine (L-Met) by cyclic voltammetry (CV), linear sweep voltammetry (LSV) and chronoamperometry. According to the results, L-Met is determined with detection limit of 30 μM. Interference studies in biological buffer was also studied. - Highlights: • The Ag-Au core-shell BNPs are synthesized and characterized • Ag-Au core-shell BNPs modified (Ag-Au/GCE) has been examined for L-methionine oxidation/sensing by using electrochemical method. • The Ag-Au/GCE exhibited good performance for the detection of L-methionine.

Synthesis of triangular Au core-Ag shell nanoparticles

International Nuclear Information System (INIS)

Rai, Akhilesh; Chaudhary, Minakshi; Ahmad, Absar; Bhargava, Suresh; Sastry, Murali

2007-01-01

In this paper, we demonstrate a simple and reproducible method for the synthesis of triangular Au core-Ag shell nanoparticles. The triangular gold core is obtained by the reduction of gold ions by lemongrass extract. Utilizing the negative charge on the gold nanotriangles, silver ions are bound to their surface and thereafter reduced by ascorbic acid under alkaline conditions. The thickness of the silver shell may be modulated by varying the pH of the reaction medium. The formation of the Au core-Ag shell triangular nanostructures has been followed by UV-vis-NIR Spectroscopy, X-ray photoelectron spectroscopy, transmission electron microscopy (TEM) and atomic force microscopy (AFM) measurements. The sharp vertices of the triangles coupled with the core-shell structure is expected to have potential for application in surface enhanced Raman spectroscopy and in the sensitive detection of biomolecules

Au@Ag core/shell cuboids and dumbbells: Optical properties and SERS response

Science.gov (United States)

Khlebtsov, Boris N.; Liu, Zhonghui; Ye, Jian; Khlebtsov, Nikolai G.

2015-12-01

Recent studies have conclusively shown that the plasmonic properties of Au nanorods can be finely controlled by Ag coating. Here, we investigate the effect of asymmetric silver overgrowth of Au nanorods on their extinction and surface-enhanced Raman scattering (SERS) properties for colloids and self-assembled monolayers. Au@Ag core/shell cuboids and dumbbells were fabricated through a seed-mediated anisotropic growth process, in which AgCl was reduced by use of Au nanorods with narrow size and shape distribution as seeds. Upon tailoring the reaction rate, monodisperse cuboids and dumbbells were synthesized and further transformed into water-soluble powders of PEGylated nanoparticles. The extinction spectra of AuNRs were in excellent agreement with T-matrix simulations based on size and shape distributions of randomly oriented particles. The multimodal plasmonic properties of the Au@Ag cuboids and dumbbells were investigated by comparing the experimental extinction spectra with finite-difference time-domain (FDTD) simulations. The SERS efficiencies of the Au@Ag cuboids and dumbbells were compared in two options: (1) individual SERS enhancers in colloids and (2) self-assembled monolayers formed on a silicon wafer by drop casting of nanopowder solutions mixed with a drop of Raman reporters. By using 1,4-aminothiophenol Raman reporter molecules, the analytical SERS enhancement factor (AEF) of the colloidal dumbbells was determined to be 5.1×106, which is an order of magnitude higher than the AEF=4.0×105 for the cuboids. This difference can be explained by better fitting of the dumbbell plasmon resonance to the excitation laser wavelength. In contrast to the colloidal measurements, the AEF=5×107 of self-assembled cuboid monolayers was almost twofold higher than that for dumbbell monolayers, as determined with rhodamine 6G Raman reporters. According to TEM data and electromagnetic simulations, the better SERS response of the self-assembled cuboids is due to uniform

Radiation annealing in Ag and Au due to energetic displacement cascades

International Nuclear Information System (INIS)

Averback, R.S.; Merkle, K.L.

1975-01-01

Radiation annealing due to energetic displacement cascades has been studied in Ag and Au. Thin film specimens, 2500 A, were doped to various concentrations of Frenkel pair defects by irradiating with 150 keV protons at temperatures below 10 K. Subsequently, the specimens were irradiated below 10 K with energetic, approximately 540 keV, self-ions. Electrical resistivity measurements were used to monitor the concentration of defects as a function of dose. In Au, approximately 5 percent of the doped-in Frenkel pairs, annealed during the 540 keV Au irradiation. The annealing volume associated with individual cascades was found to be 2.1 x 10 -16 cm 3 . In Ag approximately 5 percent of the doped-in defects annealed during a 500 keV Ag irradiation and the annealing volume of the cascade was found to be 5 x 10 -16 cm 3 . In addition, the effects of doping concentration and specimen temperature during doping were investigated

Preparation of dendritic Ag/Au bimetallic nanostructures and their application in surface-enhanced Raman scattering

International Nuclear Information System (INIS)

Yi Zao; Chen Shanjun; Chen Yan; Luo Jiangshan; Wu Weidong; Yi Yougen; Tang Yongjian

2012-01-01

Dendritic Ag/Au bimetallic nanostructures have been synthesized via a multi-stage galvanic replacement reaction of Ag dendrites in a chlorauric acid (HAuCl 4 ) solution at room temperature. After five stages of replacement reaction, one obtains structures with protruding nanocubes; these will mature into many porous structures with a few Ag atoms that are left over dendrites. The morphological and compositional changes which evolved with reaction stages were analyzed by using scanning electron microscopy, transmission electron microscopy, UV–visible spectroscopy, selected area electron diffraction and energy-dispersive X-ray spectrometry. The replacement of Ag with Au was confirmed. A formation mechanism involving the original development of Ag dendrites into porous structures with the growth of Au nanocubes on this underlying structure as the number of reaction stages is proposed. This was confirmed by surface-enhanced Raman scattering (SERS). The dendritic Ag/Au bimetallic nanostructures could be used as efficient SERS active substrates. It was found that the SERS enhancement ability was dependent on the stage of galvanic replacement reaction. - Highlights: ► Dendritic Ag/Au bimetallic nanostructures have been synthesized. ► Protruding cubic nanostructures obtained after 5 stages mature into porous structures. ► SERS results allow confirm the proposed formation mechanism. ► The nanostructures could be used as efficient SERS active substrates.

A first principles study on the electronic origins of silver segregation at the Ag-Au (111) surface

Science.gov (United States)

Hoppe, Sandra; Müller, Stefan

2017-12-01

The special electronic structure of gold gives rise to many interesting phenomena, such as its color. The surface segregation of the silver-gold system has been the subject of numerous experimental and theoretical studies, yielding conflicting results ranging from strong Ag surface enrichment to Au surface segregation. Via a combined approach of density functional theory (DFT) and statistical physics, we have analyzed the segregation at the Ag-Au (111) surface with different Ag bulk concentrations. Interestingly, we observe a moderate Au surface segregation, which is due to a charge transfer from the less electronegative Ag to Au. Canonical Monte Carlo simulations suggest that the calculated concentration profile with a Au-enriched surface layer remains stable up to higher temperatures. However, the presence of adsorbed oxygen reverses the segregation behavior and leads to strong Ag enrichment of the surface layer.

On one possibility for application of new thermoelectric materials based on Ag2Te

International Nuclear Information System (INIS)

Vassilev, Venceslav; Parvanov, Svetlin; Vachkov, Valeri

2011-01-01

The thermoelectric characteristics of Ag 2 Te and Ag 1,84 Cd 0,08 Te (solid solution based on Ag 2 Te) are investigated and analyzed. The main thermoelectric characteristics of the solid solution: α=118 μV/K; σ = 2230 S/cm and = 2,45.10 -2 W/(cm.K) ensure coefficient of thermoelectric efficiency z = 1,27. 10-3 K -1 (at 300 ), which increases this of the Ag 2 Te. A composition for commutation material is developed, which connects the N- and the P-branches of a single thermo element (52 wt. % In + 48 wt. % Sn) with melting temperature of 390 K. The possibility for application of the Ag 1,84 Cd 0,08 Te solid solution as N-branch of a thermo element in combination with the solid solution Bi 0,5 Sb 1,5 Te 3 (P-branch) is investigated. The thermo element guarantees values of z from 0,71.10 -3 to 1,27.10 -3 K -1 in the temperature interval 250 - 350 . The maximum z value is registered at 300 K (z = 1,27.10 -3 K -1 ). Keywords: Silver telluride, Solid solutions, Thermoelectric properties, Thermo element

Research Progress on AgSbTe2-based Thermoelectric Materials

Institute of Scientific and Technical Information of China (English)

CAO Qigao; MA Guang; JIA Zhihua; ZHENG Jing; LI Jin

2012-01-01

Thermoelectric power generation represents a class of energy conversion technology,which has been used in power supply of aeronautic and astronautic exploring missions,now showing notable advantages to harvest the widely distributed waste heat and convert the abundant solar energy into electricity at lower cost than Si-based photovoltaic technology.Thermoelectric dimensionless figure of merit ZT plays a key role in the conversion efficiency from thermal to electrical energy.Low thermal conductivity and large Seebeck coefficient make the AgSbTe2 compound a very promising candidate for high efficiency p-type thermoelectric applications.The AgSbTe2-based thermoelectric system has been repeatedly studied as prospective thermoelectric materials.In this review,we firstly clarify some fundamental tradeoffs dictating the ZT value through the relationship ZT =S2σT/κ.We also pay special attentions to the recent advances in AgSbTe2-based thermoelectric materials.Finally,we provide an outlook of new directions in this filed.

Electrical resistivity of liquid Ag-Au alloy

International Nuclear Information System (INIS)

Anis Alam, M.; Tomak, M.

1983-01-01

Calculations of the dependence of the electrical resistivity in liquid Ag-Au binary alloy on composition are reported. The structure of the binary alloy is described as a hard-sphere system. A one-parameter local pseudopotential, which incorporates s-d hybridization effects phenomenologically, is employed in the resistivity calculation. A reasonable agreement with experimental trend is observed. (author)

Some Applications of X-Ray Based Elemental Analysis Methods for Romanian Gold Minerals Studies

International Nuclear Information System (INIS)

Stan, D.; Constantinescu, B.; Pauna, C.; Neacsu, A.; Popescu, G.

2009-01-01

spectrometers were used for a preliminary investigation, providing only a first sample characterization due to the measurement spot size (6 mm x 5 mm). For Rosia Montana, the Au/Ag/Cu ratio is strongly variable from 14.2/4/2.9 to 1.7/2.1/0.8 and as associated minerals we found sphalerite, pyrite, chalcopyrite, galena and alabandine. For Musariu the Au/Ag/Cu ratio is strongly variable from 57.8/16.7/nd to 33.00/23.00/2.40. As associated minerals we found sphalerite, for pyrite and chalcopyrite. Using micro-PIXE at LNL Legnaro, for Rosia Montana sample the Au/Ag ratio is very different from a point to another: 53.58/16.30, 34.60/10.78, 13.83/3.75, 34.60/10.53. On the maps a weak presence of copper in the gold region in comparison with silver may be observed. Gold and silver are strongly mixed. On the outlying gold grains there are Sb, Te, Zn and also Ag-rich areas. For Musariu sample the Au/Ag/Cu ratio is strongly variable from 3.24/0.42/0.0027, 6.05/1.32/0.0217 to 19.13/4.19/0.0078. In the case of the Musariu ore deposit gold, silver and copper are evidently mixed; a strong presence of copper is observed. A significant amount of Si (quartz) was observed surrounding the gold grains. On the distribution map, Zn-rich areas are observed, beside Au, Sb, and less Ag. There are some metallic Cu-points, Fe-points (pyrite), Pb-points (galena), Mn-points (alabandine) and native As-rich points. As characteristic trace elements, we found from BESSY micro-SR-XRF point spectra measurements local relatively large (up to 1500 ppm) amounts of Te and moderate (100-150 ppm) of Sb in Rosia Montana and also local relatively important (350-500 ppm) quantities of Sb in Musariu.

Characteristics of hydrothermal alteration mineralogy and geochemistry of igneous rocks from the epithermal Co-O mine and district, Eastern Mindanao (Philippines)

Science.gov (United States)

Sonntag, Iris; Hagemann, Steffen

2010-05-01

Detailed petrographic as well as hyperspectral analyses using PIMA (Portable Infrared Mineral Analyser) and geochemical (major, trace and rare earth elements) studies were conducted on samples of the epithermal, low sulfidation Co-O mine (47,869 ounces gold produced in 2009 with an average grade of 13.3 g/t gold) and district in Eastern Mindanao (Philippines). The aims of the study were to unravel the petrogenetic origin of the various volcanic (host rocks) and intrusive rocks (potential fluid driver) as well as their relationship and influence on the hydrothermal alteration zoning and fluid chemistry. The auriferous veins at the Co-O mine were formed during two hydrothermal stages associated with the district wide D1 and D2 deformation events. Gold in stage 1 quartz veins is in equilibrium with galena and sphalerite, whereas in stage 2 it is associated with pyrite. Auriferous quartz veins of stage 1 reflect temperatures below 250° C or strong variations in pH and fO2 at higher temperatures, due to potential involvement of acidic gas or meteoric water. Cathodoluminescense studies revealed strong zonation of quartz associated with Au, presumably related to changes in the Al content, which is influenced by the pH. Plumose textures indicate times of rapid deposition, whereas saccharoidal quartz grains are related to potential calcite replacement. The geology of the Co-O mine and district is dominated by Miocene volcanic rocks (basic to intermediate flows and pyroclastics units), which are partly covered by Pliocene volcanic rocks and late Oligocene to Miocene limestones. The Miocene units are intruded by diorite (presumably Miocene in age). The epithermal mineralization event may be related to diorite intrusions. The geochemistry of all igneous rocks in the district is defined by a sub-alkaline affinity and is low to medium K in composition. Most units are related to a Miocene subduction zone with westward subduction, whereas the younger Pliocene rocks are related to

1-Hexadecylamine as both reducing agent and stabilizer to synthesize Au and Ag nanoparticles and their SERS application

International Nuclear Information System (INIS)

Hou Xiaomiao; Zhan, Xiaoling; Fang Yan; Chen Shutang; Li Na; Zhou Qi

2011-01-01

1-Hexadecylamine (HDA)-capped Au and Ag nanoparticles (NPs) have been successfully prepared by a one-pot solution growth method. The HDA is used as both reducing agent and stabilizer in the synthetic process is favorable for investigating the capping mechanism of Au and Ag NPs’ surface. The growth process and characterization of Au and Ag NPs are determined by Ultraviolet–visible (UV–vis) spectroscopy, transmission electron microscopy (TEM), and X-ray diffraction (XRD). Experimental results demonstrate that the HDA-capped Au and Ag NPs are highly crystalline and have good optical properties. Furthermore, surface-enhanced Raman scattering (SERS) spectra of 2-thionaphthol are obtained on the Au and Ag NPs modified glass surface, respectively, indicating that the as-synthesized noble metal NPs have potentially high sensitive optical detection application.

1-Hexadecylamine as both reducing agent and stabilizer to synthesize Au and Ag nanoparticles and their SERS application

Energy Technology Data Exchange (ETDEWEB)

Hou Xiaomiao; Zhan, Xiaoling, E-mail: zhangxl@bit.edu.cn [Beijing Institute of Technology, Department of Chemistry, School of Science (China); Fang Yan, E-mail: fangyan@mail.cnu.edu.cn [Capital Normal University, Beijing Key Lab for Nano-Photonics and Nano-Structure (NPNS), Department of Physics (China); Chen Shutang; Li Na; Zhou Qi [Beijing Institute of Technology, Department of Chemistry, School of Science (China)

2011-05-15

1-Hexadecylamine (HDA)-capped Au and Ag nanoparticles (NPs) have been successfully prepared by a one-pot solution growth method. The HDA is used as both reducing agent and stabilizer in the synthetic process is favorable for investigating the capping mechanism of Au and Ag NPs' surface. The growth process and characterization of Au and Ag NPs are determined by Ultraviolet-visible (UV-vis) spectroscopy, transmission electron microscopy (TEM), and X-ray diffraction (XRD). Experimental results demonstrate that the HDA-capped Au and Ag NPs are highly crystalline and have good optical properties. Furthermore, surface-enhanced Raman scattering (SERS) spectra of 2-thionaphthol are obtained on the Au and Ag NPs modified glass surface, respectively, indicating that the as-synthesized noble metal NPs have potentially high sensitive optical detection application.

Measurement of the neutron flux distributions, epithermal index, Westcott thermal neutron flux in the irradiation capsules of hydraulic conveyer (Hyd) and pneumatic tubes (Pn) facilities of the KUR

International Nuclear Information System (INIS)

Chatani, Hiroshi

2001-05-01

The reactions of Au(n, γ) 198 Au and Ti(n, p) 47 or 48 Sc were used for the measurements of the thermal and epithermal (thermal + epithermal) and the fast neutron flux distributions, respectively. In the case of Hyd (Hydraulic conveyer), the thermal + epithermal and fast neutron flux distributions in the horizontal direction in the capsule are especially flat; the distortion of the fluxes are 0.6% and 5.4%, respectively. However, these neutron fluxes in the vertical direction are low at the top and high at the bottom of the capsule. These differences between the top and bottom are 14% for both distributions. On the other hand, in polyethylene capsules of Pn-1, 2, 3 (Pneumatic tubes Nos. 1, 2, 3), in contrast with Hyd, these neutron flux distributions in the horizontal direction have gradients of 8 - 18% per 2.5 cm diameter, and those on the vertical axis have a distortion of approximately 5%. The strength of the epithermal dE/E component relative to the neutron density including both thermal and epithermal neutrons, i.e., the epithermal index, for the hydraulic conveyer (Hyd) and pneumatic tube No.2 (Pn-2), in which the irradiation experiments can be achieved, are determined by the multiple foil activation method using the reactions of Au(n, γ) 198 Au and Co(n, γ) 60(m+g) Co. The epithermal index observed in an aluminum capsule of Hyd is 0.034-0.04, and the Westcott thermal neutron flux is 1.2x10 14 cm -2 sec -1 at approximately 1 cm above the bottom. The epithermal index in a Pn-2 polyethylene capsule was measured by not only the multiple foil activation method but also the Cd-ratio method in which the Au(n, γ) 198 Au reaction in a cadmium cover is also used. The epithermal index is 0.045 - 0.055, and the thermal neutron flux is 1.8x10 13 cm -2 sec -1 . (J.P.N.)

Microstructure analyses and thermoelectric properties of Ag1−xPb18Sb1+yTe20

International Nuclear Information System (INIS)

Perlt, S.; Höche, Th.; Dadda, J.; Müller, E.; Bauer Pereira, P.; Hermann, R.; Sarahan, M.; Pippel, E.; Brydson, R.

2012-01-01

This study reports microstructural investigations of long-term annealed Ag 1−x Pb m Sb 1+y Te 2+m (m=18, x=y=0, hereinafter referred to as AgPb 18 SbTe 20 ) (Lead–Antimony–Silver–Tellurium, LAST-18) as well as of Ag 1−x Pb 18 Sb 1+y Te 20 , i.e. Ag-deficient and Sb-excess LAST-18 (x≠0,y≠0), respectively. Two different length scales are explored. The micrometer scale was evaluated by SEM to analyze the volume fraction and the number of secondary phases as well as the impact of processing parameters on the homogeneity of bulk samples. For AgPb 18 SbTe 20 , site-specific FIB liftout of TEM lamellae from thermoelectrically characterized samples was accomplished to investigate the structure on the nanometer scale. High-resolution TEM and energy-filtered TEM were performed to reveal shape and size distribution of nanoprecipitates, respectively. A hypothesis concerning the structure–property relationship is set out within the frame of a gradient annealing experiment. This study is completed by results dealing with inhomogeneities on the micrometer scale of Ag 1−x Pb 18 Sb 1+y Te 20 and its electronic properties. Highlights: ► SEM and TEM microstructure investigation of long-term annealed AgPb 18 SbTe 20 . ► SEM and thermoelectric studies on Ag 1−x Pb 18 Sb 1+y Te 20 . ► Discussion concerning structure–property relationship in long-term annealed AgPb 18 SbTe 20 . ► Correlation between Ag 1−x Pb 18 Sb 1+y Te 20 microscale structure and electronic properties.

Highly open bowl-like PtAuAg nanocages as robust electrocatalysts towards ethylene glycol oxidation

Science.gov (United States)

Xu, Hui; Yan, Bo; Li, Shumin; Wang, Jin; Song, Pingping; Wang, Caiqin; Guo, Jun; Du, Yukou

2018-04-01

A novel combined seed mediated and galvanic replacement method has been demonstrated to synthesize a new class of trimetallic PtAuAg nanocatalysts with highly open bowl-like nanocage structure. The newly-generated PtAuAg nanocages catalysts exhibit superior electrocatalytic performances towards ethylene glycol oxidation with the mass activity of 6357.1 mA mg-1, 5.5 times higher than that of commercial Pt/C (1151.1 mA mg-1). This work demonstrates the first example of designing shape-controlled architectures of trimetallic bowl-like PtAuAg nanocages for liquid fuel electrooxidation.

Size and composition tunable Ag-Au alloy nanoparticles by replacement reactions

International Nuclear Information System (INIS)

Zhang Qingbo; Lee, J Y; Yang Jun; Boothroyd, Chris; Zhang Jixuan

2007-01-01

Ag-Au alloy nanoparticles with tunable size and composition were prepared by a replacement reaction between Ag nanoparticles and HAuCl 4 at elevated temperatures. The formation of homogeneous alloy nanoparticles was confirmed by selected-area energy-dispersive x-ray spectroscopy (SAEDX), UV-visible absorption spectroscopy, high resolution transmission electron microscopy (HRTEM) and electron diffraction. This method leverages upon the rapid interdiffusion of Ag and Au atoms in the reduced dimension of a nanoparticle, elevated temperatures and the large number of vacancy defects created in the replacement reaction. This method of preparation has several notable advantages: (1) independent tuning of the size and composition of alloy nanoparticles; (2) production of alloy nanoparticles in high concentrations; (3) general utility in the synthesis of alloy nanoparticles that cannot be obtained by the co-reduction method

Some recent results in Au+Au collisions at AGS

International Nuclear Information System (INIS)

Chen, Z.

1996-01-01

Many interesting results have been obtained for Au + Au reactions at AGS. The basic information about the reaction dynamics comes from the hadronic distribution. and this article reviews the recent progress of these distributions in details. The proton rapidity distribution shows significantly increased stopping compared to lighter systems, implying the formation of a state of high baryon density. Unlike reactions at this energy induced by lighter heavy ions, at low m t - m 0 the proton invariant spectra deviate from a single exponential shape and become fear,. while pion spectra are found to rise in this region, with the π - spectra rising faster than the π + spectra. The inverse slope parameter increases faster for particles of larger mass as the number of participants in the reaction increases, an indication of increased effect of radial expansion in central collision. Anti-proton Needs have been measured recently, and unfortunately a comparison among current results from different experiments indicates discrepancy

Covellite CuS as a matrix for "invisible" gold: X-ray spectroscopic study of the chemical state of Cu and Au in synthetic minerals

Science.gov (United States)

Tagirov, Boris R.; Trigub, Alexander L.; Kvashnina, Kristina O.; Shiryaev, Andrey A.; Chareev, Dmitriy A.; Nickolsky, Maximilian S.; Abramova, Vera D.; Kovalchuk, Elena V.

2016-10-01

Geological processes leading to formation of sulfide ores often result in precipitation of gold-bearing sulfides which can contain high concentrations of this metal in ;invisible; (or ;refractory;) state. Covellite (CuS) is ubiquitous mineral in many types of the ore deposits, and numerous studies of the natural ores show that covellite can contain high concentrations of Au. At the same time, Au-bearing covellite withstands cooling in contrast to other minerals of the Cu-Fe-S system (chalcocite, bornite, chalcopyrite), where Au exsolves at low temperatures. This makes covellite a convenient model system for investigation of the chemical state (local environment and valence) of the ;invisible; Au in copper-sulfide ores (copper-porphyry, epithermal, volcanogenic massive sulfide, SEDEX deposits). Therefore, it is necessary to determine the location of Au in the covellite matrix as it will have important implications for the methods employed by mineral processing industry to extract Au from sulfide ores. Here we investigate the chemical state of Cu and Au in synthetic covellite containing up to 0.3 wt.% of Au in the ;invisible; state. The covellite crystals were synthesized by hydrothermal and salt flux methods. Formation of the chemically bound Au is indicated by strong dependence of the concentration of Au in covellite on the sulfur fugacity in the experimental system (d(log C(Au))/d(log f(S2)) ∼ 0.65). The Au concentration of covellite grows with increasing temperature from 400 to 450 °C, whereas further temperature increase to 500 °C has only minor effect. The synthesized minerals were studied using X-ray absorption fine structure spectroscopy (XAFS) in high energy resolution fluorescence detection (HERFD) mode. Ab initio simulations of Cu K edge XANES spectra show that the Cu oxidation state in two structural positions in covellite (tetrahedral and triangular coordination with S atoms) is identical: the total loss of electronic charge for the 3d shell is ∼0

The crystal structure of sopcheite, Ag.sub.4./sub.Pd.sub.3./sub.Te.sub.4./sub., from the Lukkulaisvaara intrusion, Karelia, Russia

Czech Academy of Sciences Publication Activity Database

Laufek, F.; Vymazalová, A.; Grokhovskaya, T.L.; Plášil, Jakub; Dušek, Michal; Orsoev, D.A.; Kozlov, V.V.

2017-01-01

Roč. 29, Jun (2017), s. 603-612 ISSN 0935-1221 Institutional support: RVO:68378271 Keywords : sopcheite * crystal structure * Ag4Pd3Te4 * platinum-group mineral * silver palladium telluride * X-ray diffraction data * Lukkulaisvaara intrusion Subject RIV: DB - Geology ; Mineralogy OBOR OECD: Geology Impact factor: 1.362, year: 2016

TEM investigation of the topotactic reaction of (001) and (111) Ag films and Te

International Nuclear Information System (INIS)

Safran, G.; Geszti, O.; Radnoczi, G.

2002-01-01

The formation, structure and morphology of Ag 2 Te phase developed by the reaction of single crystalline Ag films with subsequently vacuum deposited Te vapour was investigated. Silver films 30-40 nm in thickness were deposited at 85-120 grad C by thermal evaporation in vacuum at a base pressure of 4x10 -5 mbar. The NaCl substrates were cleaved and saw-cut in order to achieve (001) and (111) surfaces, respectively. The surfaces were treated with water and chlorine prior to Ag deposition. This preparation resulted in single crystalline Ag films of (001) and (111) orientation. Tellurium was deposited onto the silver at a rate about 0.1 nm/s at 200 grad C i.e. above the temperature of the polymorphic phase transformation from monoclinic to fcc (T c =150 grad C). The Ag-Te reaction occurred during the Te deposition. The samples were investigated by TEM and SAED in a 200 kV Philips CM 20 electron microscope equipped with a Ge detector Noran EDS system. In the fully tellurized layers, however, the monoclinic (low temperature) Ag 2 Te phase was found. It exhibited large single crystals consisting of strictly oriented mosaic grains of 1-2 mm size. Surprisingly, the orientation of the telluride was identical (010) on both the (001) and (111) Ag parent films. It is suggested that the final orientation appears during the polymorphic phase transition while cooling to room temperature, regardless to Ag orientation, due to the lower surface energy of the (010) orientation of monoclinic phase nuclei. (Authors)

Determination of silver using cyclic epithermal neutron activation analysis

International Nuclear Information System (INIS)

Pun, T.H.; Landsberger, S.

2012-01-01

A fast pneumatic transfer facility was installed in Nuclear Engineering Teaching Laboratory (NETL) of the University of Texas at Austin for the purpose of cyclic thermal and epithermal neutron activation analysis. In this study efforts were focused on the evaluation of cyclic epithermal neutron activation analysis (CENAA). Various NIST and CANMET certified materials were analyzed by the system. Experiment results showed 110 Ag with its 25 s half-life as one of the isotopes favored by the system. Thus, the system was put into practical application in identifying silver in metallic ores. Comparison of sliver concentrations as determined by CENAA in CANMET certified reference materials gave very good results. (author)

First-principles theory of short-range order in size-mismatched metal alloys: Cu-Au, Cu-Ag, and Ni-Au

International Nuclear Information System (INIS)

Wolverton, C.; Ozolins, V.; Zunger, A.

1998-01-01

We describe a first-principles technique for calculating the short-range order (SRO) in disordered alloys, even in the presence of large anharmonic atomic relaxations. The technique is applied to several alloys possessing large size mismatch: Cu-Au, Cu-Ag, Ni-Au, and Cu-Pd. We find the following: (i) The calculated SRO in Cu-Au alloys peaks at (or near) the left-angle 100 right-angle point for all compositions studied, in agreement with diffuse scattering measurements. (ii) A fourfold splitting of the X-point SRO exists in both Cu 0.75 Au 0.25 and Cu 0.70 Pd 0.30 , although qualitative differences in the calculated energetics for these two alloys demonstrate that the splitting in Cu 0.70 Pd 0.30 may be accounted for by T=0 K energetics while T≠0 K configurational entropy is necessary to account for the splitting in Cu 0.75 Au 0.25 . Cu 0.75 Au 0.25 shows a significant temperature dependence of the splitting, in agreement with recent in situ measurements, while the splitting in Cu 0.70 Pd 0.30 is predicted to have a much smaller temperature dependence. (iii) Although no measurements exist, the SRO of Cu-Ag alloys is predicted to be of clustering type with peaks at the left-angle 000 right-angle point. Streaking of the SRO peaks in the left-angle 100 right-angle and left-angle 1 (1) /(2) 0 right-angle directions for Ag- and Cu-rich compositions, respectively, is correlated with the elastically soft directions for these compositions. (iv) Even though Ni-Au phase separates at low temperatures, the calculated SRO pattern in Ni 0.4 Au 0.6 , like the measured data, shows a peak along the left-angle ζ00 right-angle direction, away from the typical clustering-type left-angle 000 right-angle point. (v) The explicit effect of atomic relaxation on SRO is investigated and it is found that atomic relaxation can produce significant qualitative changes in the SRO pattern, changing the pattern from ordering to clustering type, as in the case of Cu-Ag. copyright 1998 The American

On interface dipole layers between C60 and Ag or Au

NARCIS (Netherlands)

Veenstra, Sjoerd; Heeres, A.; Hadziioannou, G.; Sawatzky, G.A.; Jonkman, H.T.

2002-01-01

C60 layers on polycrystalline Ag and Au are studied by photoelectron spectroscopy. At these metal/C60 interfaces an electron transfer occurs from the metal to the lowest unoccupied orbital of C60. We found in the case of the polycrystalline Ag/C60 interface a dipolar layer with its associated

Nanoscale clusters in the high performance thermoelectric AgPb{sub m}SbTe{sub m+2}

Energy Technology Data Exchange (ETDEWEB)

Lin, H; Bozin, E S; Billinge, S J.L.; Quarez, Eric; Kanatzidis, M G [Department of Physics and Astronomy, Michigan State University, East Lansing, Michigan 48824 (United States); Department of Chemistry, Michigan State University, East Lansing, Michigan 48824 (United States)

2005-11-01

The local structure of the AgPb{sub m}SbTe{sub m+2} series of thermoelectric materials has been studied using the atomic pair distribution function (PDF) method. Three candidate-models were attempted for the structure of this class of materials using either a one- or a two-phase modeling procedure. Combining modeling the PDF with HRTEM data we show that AgPb{sub m}SbTe{sub m+2} contains nanoscale inclusions with composition close to AgPb{sub 3}SbTe{sub 5} randomly embedded in a PbTe matrix.

Stepwise synthesis of cubic Au-AgCdS core-shell nanostructures with tunable plasmon resonances and fluorescence.

Science.gov (United States)

Liu, Xiao-Li; Liang, Shan; Nan, Fan; Pan, Yue-Yue; Shi, Jun-Jun; Zhou, Li; Jia, Shuang-Feng; Wang, Jian-Bo; Yu, Xue-Feng; Wang, Qu-Quan

2013-10-21

Cubic Au-AgCdS core-shell nanostructures were synthesized through cation exchange method assisted by tributylphosphine (TBP) as a phase-transfer agent. Among intermediate products, Au-Ag core-shell nanocubes exhibited many high-order plasmon resonance modes related to the special cubic shape, and these plasmon bands red-shifted along with the increasing of particle size. The plasmon band of Au core first red-shifted and broadened at the step of Au-Ag₂S and then blue-shifted and narrowed at the step of Au-AgCdS. Since TBP was very crucial for the efficient conversion from Ag₂S to CdS, we found that both absorption and fluorescence of the final products could be controlled by TBP.

Particle growth mechanisms in Ag-ZrO2 and Au-ZrO2 granular films obtained by pulsed laser deposition

International Nuclear Information System (INIS)

Konstantinovic, Zorica; Muro, Montserrat Garcia del; Varela, Manuel; Batlle, Xavier; Labarta, AmIlcar

2006-01-01

Thin films consisting of Ag and Au nanoparticles embedded in amorphous ZrO 2 matrix were grown by pulsed laser deposition in a wide range of metal volume concentrations in the dielectric regime (0.08 Ag Au c (Ag)∼0.28 and x c (Au)∼0.52)

Formation of nanodots and enhancement of thermoelectric power induced by ion irradiation in PbTe:Ag composite thin films

Energy Technology Data Exchange (ETDEWEB)

Bala, Manju, E-mail: manjubala474@gmail.com [Inter-University Accelerator Centre, Aruna Asaf Ali Marg, New Delhi 110067 (India); Meena, Ramcharan; Gupta, Srashti; Pannu, Compesh [Inter-University Accelerator Centre, Aruna Asaf Ali Marg, New Delhi 110067 (India); Tripathi, Tripurari S. [Aalto University, Värmemansgränden 2, 02150 Espoo (Finland); Varma, Shikha [Institute of Physics, Bhubaneshwar, Odisha 751005 (India); Tripathi, Surya K. [Department of Physics, Panjab University, Chandigarh 160 014 (India); Asokan, K., E-mail: asokaniuac@gmail.com [Inter-University Accelerator Centre, Aruna Asaf Ali Marg, New Delhi 110067 (India); Avasthi, Devesh K. [Amity University, Noida 201313, Uttar Pradesh (India)

2016-07-15

Present study demonstrates an enhancement in thermoelectric power of 10% Ag doped PbTe (PbTe:Ag) thin films when irradiated with 200 keV Ar ion. X-ray diffraction showed an increase in crystallinity for both PbTe and PbTe:10Ag nano-composite films after Ar ion irradiation due to annealing of defects in the grain boundaries. The preferential sputtering of Pb and Te ions in comparison to Ag ions resulted in the formation of nano-dots. This was further confirmed by X-ray photoelectron spectroscopy (XPS). Such an enhancement in thermoelectric power of irradiated PbTe:10Ag films in comparison to pristine PbTe:10Ag film is attributed to the decrease in charge carrier concentration that takes part in the transport process via restricting the tunneling of carriers through the wider potential barrier formed at the interface of nano-dots.

Tuning the shell thickness-dependent plasmonic absorption of Ag coated Au nanocubes: The effect of synthesis temperature

Energy Technology Data Exchange (ETDEWEB)

Zhu, Jian, E-mail: jianzhusummer@163.com; Zhang, Fan; Chen, Bei-Bei; Li, Jian-Jun; Zhao, Jun-Wu, E-mail: nanoptzhao@163.com

2015-09-15

Graphical abstract: Ag coating leads to great enhancement of SPR absorbance of Au nanocubes, and the Ag coating-dependent non-monotonous SPR shift is greater at lower temperature. - Highlights: • Au nanocubes with more uniform shape can be obtained at lower growth temperature. • Ag coating leads to great enhancement of SPR absorption intensity. • The Ag coating dependent non-monotonous SPR shift is greater at lower temperature. - Abstract: The temperature dependent synthesis and plasmonic optical properties of Ag coated Au nanocubes have been investigated experimentally. It has been found that the Au nanocubes with more uniform morphology and higher yield could be obtained by decreasing the growth temperature. Because of the non-spherical symmetry of the particles shape and the plasmon coupling between Au–Ag interface and outer Ag surface, four absorption peaks at most have been observed. As the Ag coating thickness is increased, the absorbance intensity of these plasmon peaks gets intense greatly, and the absorption peak at longest wavelength blue shifts firstly and then red shifts. The non-monotonous plasmonic shift has been attributed to the competition between the increase of Ag composition and the enlargement of the particle size. What's more, the wavelength region of both blue shift and red shift could also be enhanced by decreasing the temperature.

Tuning the shell thickness-dependent plasmonic absorption of Ag coated Au nanocubes: The effect of synthesis temperature

International Nuclear Information System (INIS)

Zhu, Jian; Zhang, Fan; Chen, Bei-Bei; Li, Jian-Jun; Zhao, Jun-Wu

2015-01-01

Graphical abstract: Ag coating leads to great enhancement of SPR absorbance of Au nanocubes, and the Ag coating-dependent non-monotonous SPR shift is greater at lower temperature. - Highlights: • Au nanocubes with more uniform shape can be obtained at lower growth temperature. • Ag coating leads to great enhancement of SPR absorption intensity. • The Ag coating dependent non-monotonous SPR shift is greater at lower temperature. - Abstract: The temperature dependent synthesis and plasmonic optical properties of Ag coated Au nanocubes have been investigated experimentally. It has been found that the Au nanocubes with more uniform morphology and higher yield could be obtained by decreasing the growth temperature. Because of the non-spherical symmetry of the particles shape and the plasmon coupling between Au–Ag interface and outer Ag surface, four absorption peaks at most have been observed. As the Ag coating thickness is increased, the absorbance intensity of these plasmon peaks gets intense greatly, and the absorption peak at longest wavelength blue shifts firstly and then red shifts. The non-monotonous plasmonic shift has been attributed to the competition between the increase of Ag composition and the enlargement of the particle size. What's more, the wavelength region of both blue shift and red shift could also be enhanced by decreasing the temperature

Au@Ag Core-Shell Nanocubes with Finely Tuned and Well-Controlled Sizes, Shell Thicknesses, and Optical Properties

OpenAIRE

Ma, Yanyun; Li, Weiyang; Cho, Eun Chul; Li, Zhiyuan; Yu, Taekyung; Zeng, Jie; Xie, Zhaoxiong; Xia, Younan

2010-01-01

This paper describes a facile method for generating Au@Ag core-shell nanocubes with edge lengths controllable in the range of 13.4 to 50 nm. The synthesis involved the use of single-crystal, spherical Au nanocrystals of 11 nm in size as the seeds in an aqueous system, with ascorbic acid serving as the reductant and cetyltrimethylammonium chloride (CTAC) as the capping agent. The thickness of the Ag shells could be finely tuned from 1.2 to 20 nm by varying the ratio of AgNO3 precursor to Au se...

Electronic structures of PtCu, PtAg, and PtAu molecules: a Dirac four-component relativistic study

International Nuclear Information System (INIS)

Abe, Minori; Mori, Sayaka; Nakajima, Takahito; Hirao, Kimihiko

2005-01-01

Relativistic four-component calculations at several correlated levels have been performed for diatomic PtCu, PtAg, and PtAu molecules. The ground state spectroscopic constants of PtCu were calculated using the four-component MP2 method, and show good agreement with experiment. We also performed calculations on the experimentally unknown species, PtAg and PtAu, and the mono-cationic systems, PtCu + , PtAg + , and PtAu + . The low-lying excited states of these diatomic molecules were also investigated using the four-component multi-reference CI method

Onset of Intense Surface Enhanced Raman Scattering and Aggregation in the Au@Ag System

Directory of Open Access Journals (Sweden)

Priya Bhatia

2015-01-01

Full Text Available Gold core/silver shell (Au@Ag nanoparticles of ~37 ± 5 nm diameter generate intense SERS (λEX=785 nm responses in solution when they interact with the SERS labels rhodamine 6G (R6G, 4-mercaptopyridine (MPY, and 4-mercaptobenzoic acid (MBA. Herein the relationship between SERS intensity, aggregation, and adsorption phenomenon isobserved by titrating Au@Ag with the above labels. As the labels adsorb to the Au@Ag, they drive aggregation as evidenced by the creation of NIR extinction peaks, and the magnitude of this NIR extinction (measured at 830 nm correlates very closely to magnitude of the intense SERS signals. The label MBA is an exception since it does not trigger aggregation nor does it result in intense SERS; rather intense SERS is recovered only after MBA coated Au@Ag is aggregated with KCl. An “inner filter” model is introduced and applied to compensate for solution extinction when the exciting laser radiation is significantly attenuated. This model permits a summary of the SERS responses in the form of plots of SERS intensity versus the aggregate absorption at 830 nm, which shows the excellent correlation between intense SERS and LSPR bands extinction.

Synthesis of Au@Ag core-shell nanocubes containing varying shaped cores and their localized surface plasmon resonances.

Science.gov (United States)

Gong, Jianxiao; Zhou, Fei; Li, Zhiyuan; Tang, Zhiyong

2012-06-19

We have synthesized Au@Ag core-shell nanocubes containing Au cores with varying shapes and sizes through modified seed-mediated methods. Bromide ions are found to be crucial in the epitaxial growth of Ag atoms onto Au cores and in the formation of the shell's cubic shape. The Au@Ag core-shell nanocubes exhibit very abundant and distinct localized surface plasmon resonance (LSPR) properties, which are core-shape and size-dependent. With the help of theoretical calculation, the physical origin and the resonance mode profile of each LSPR peak are identified and studied. The core-shell nanocrystals with varying shaped cores offer a new rich category for LSPR control through the plasmonic coupling effect between core and shell materials.

Application of Direct Current Atmospheric Pressure Glow Microdischarge Generated in Contact with a Flowing Liquid Solution for Synthesis of Au-Ag Core-Shell Nanoparticles.

Science.gov (United States)

Dzimitrowicz, Anna; Jamroz, Piotr; Nyk, Marcin; Pohl, Pawel

2016-04-06

A direct current atmospheric pressure glow microdischarge (dc-μAPGD) generated between an Ar nozzle microjet and a flowing liquid was applied to produce Au-Ag core-shell nanoparticles (Au@AgCSNPs) in a continuous flow system. Firstly, operating dc-μAPGD with the flowing solution of the Au(III) ions as the cathode, the Au nanoparticles (AuNPs) core was produced. Next, to produce the core-shell nanostructures, the collected AuNPs solution was immediately mixed with an AgNO₃ solution and passed through the system with the reversed polarity to fabricate the Ag nanoshell on the AuNPs core. The formation of Au@AgCSNPs was confirmed using ultraviolet-visible (UV-Vis) absorbance spectrophotometry, transmission electron microscopy (TEM), and energy-dispersive X-ray spectroscopy (EDS). Three localized surface plasmon resonance absorption bands with wavelengths centered at 372, 546, and 675 nm were observed in the UV-Vis spectrum of Au@AgCSNPs, confirming the reduction of both the Au(III) and Ag(I) ions. The right configuration of metals in Au@AgCSNPs was evidenced by TEM. The Au core diameter was 10.2 ± 2.0 nm, while the thickness of the Ag nanoshell was 5.8 ± 1.8 nm. The elemental composition of the bimetallic nanoparticles was also confirmed by EDS. It is possible to obtain 90 mL of a solution containing Au@AgCSNPs per hour using the applied microdischarge system.

Bottom-up processing of thermoelectric nanocomposites from colloidal nanocrystal building blocks: the case of Ag{sub 2}Te-PbTe

Energy Technology Data Exchange (ETDEWEB)

Cadavid, Doris [Catalonia Institute for Energy Research, IREC (Spain); Ibanez, Maria [Universitat de Barcelona, Departament d' Electronica (Spain); Gorsse, Stephane [Universite de Bordeaux, ICMCB, CNRS (France); Lopez, Antonio M. [Universitat Politecnica de Catalunya, Departament d' Enginyeria Electronica (Spain); Cirera, Albert [Universitat de Barcelona, Departament d' Electronica (Spain); Morante, Joan Ramon; Cabot, Andreu, E-mail: acabot@irec.cat [Catalonia Institute for Energy Research, IREC (Spain)

2012-12-15

Nanocomposites are highly promising materials to enhance the efficiency of current thermoelectric devices. A straightforward and at the same time highly versatile and controllable approach to produce nanocomposites is the assembly of solution-processed nanocrystal building blocks. The convenience of this bottom-up approach to produce nanocomposites with homogeneous phase distributions and adjustable composition is demonstrated here by blending Ag{sub 2}Te and PbTe colloidal nanocrystals to form Ag{sub 2}Te-PbTe bulk nanocomposites. The thermoelectric properties of these nanocomposites are analyzed in the temperature range from 300 to 700 K. The evolution of their electrical conductivity and Seebeck coefficient is discussed in terms of the blend composition and the characteristics of the constituent materials.

Leaching of Au, Ag, and Pd from waste printed circuit boards of mobile phone by iodide lixiviant after supercritical water pre-treatment

International Nuclear Information System (INIS)

Xiu, Fu-Rong; Qi, Yingying; Zhang, Fu-Shen

2015-01-01

Highlights: • We report a novel process for recovering Au, Ag, and Pd from waste PCBs. • The effect of SCWO on the leaching of Au, Ag, and Pd in waste PCBs was studied. • SCWO was highly efficient for enhancing the leaching of Au, Ag, and Pd. • The optimum leaching parameters for Au, Ag, and Pd in iodine–iodide were studied. - Abstract: Precious metals are the most attractive resources in waste printed circuit boards (PCBs) of mobile phones. In this work, an alternative process for recovering Au, Ag, and Pd from waste PCBs of mobile phones by supercritical water oxidation (SCWO) pre-treatment combined with iodine–iodide leaching process was developed. In the process, the waste PCBs of mobile phones were pre-treated in supercritical water, then a diluted hydrochloric acid leaching (HL) process was used to recovery the Cu, whose leaching efficiency was approximately 100%, finally the resulting residue was subjected to the iodine–iodide leaching process for recovering the Au, Ag, and Pd. Experimental results indicated that SCWO pre-treatment temperature, time, and pressure had significant influence on the Au, Ag, and Pd leaching from (SCWO + HL)-treated waste PCBs. The optimal SCWO pre-treatment conditions were 420 °C and 60 min for Au and Pd, and 410 °C and 30 min for Ag. The optimum dissolution parameters for Au, Pd, and Ag in (SCWO + HL)-treated PCBs with iodine–iodide system were leaching time of 120 min (90 min for Ag), iodine/iodide mole ratio of 1:5 (1:6 for Ag), solid-to-liquid ratio (S/L) of 1:10 g/mL (1:8 g/mL for Ag), and pH of 9, respectively. It is believed that the process developed in this study is environment friendly for the recovery of Au, Ag, and Pd from waste PCBs of mobile phones by SCWO pre-treatment combined with iodine–iodide leaching process

Leaching of Au, Ag, and Pd from waste printed circuit boards of mobile phone by iodide lixiviant after supercritical water pre-treatment

Energy Technology Data Exchange (ETDEWEB)

Xiu, Fu-Rong, E-mail: xiu_chem@hotmail.com [College of Ecological Environment and Urban Construction, Fujian University of Technology, Fuzhou 350108 (China); Qi, Yingying [College of Ecological Environment and Urban Construction, Fujian University of Technology, Fuzhou 350108 (China); Zhang, Fu-Shen [Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China)

2015-07-15

Highlights: • We report a novel process for recovering Au, Ag, and Pd from waste PCBs. • The effect of SCWO on the leaching of Au, Ag, and Pd in waste PCBs was studied. • SCWO was highly efficient for enhancing the leaching of Au, Ag, and Pd. • The optimum leaching parameters for Au, Ag, and Pd in iodine–iodide were studied. - Abstract: Precious metals are the most attractive resources in waste printed circuit boards (PCBs) of mobile phones. In this work, an alternative process for recovering Au, Ag, and Pd from waste PCBs of mobile phones by supercritical water oxidation (SCWO) pre-treatment combined with iodine–iodide leaching process was developed. In the process, the waste PCBs of mobile phones were pre-treated in supercritical water, then a diluted hydrochloric acid leaching (HL) process was used to recovery the Cu, whose leaching efficiency was approximately 100%, finally the resulting residue was subjected to the iodine–iodide leaching process for recovering the Au, Ag, and Pd. Experimental results indicated that SCWO pre-treatment temperature, time, and pressure had significant influence on the Au, Ag, and Pd leaching from (SCWO + HL)-treated waste PCBs. The optimal SCWO pre-treatment conditions were 420 °C and 60 min for Au and Pd, and 410 °C and 30 min for Ag. The optimum dissolution parameters for Au, Pd, and Ag in (SCWO + HL)-treated PCBs with iodine–iodide system were leaching time of 120 min (90 min for Ag), iodine/iodide mole ratio of 1:5 (1:6 for Ag), solid-to-liquid ratio (S/L) of 1:10 g/mL (1:8 g/mL for Ag), and pH of 9, respectively. It is believed that the process developed in this study is environment friendly for the recovery of Au, Ag, and Pd from waste PCBs of mobile phones by SCWO pre-treatment combined with iodine–iodide leaching process.

A review of Pb-Sb(As-S, Cu(Ag-Fe(Zn-Sb(As-S, Ag(Pb-Bi(Sb-S and Pb-Bi-S(Te sulfosalt systems from the Boranja orefield, West Serbia

Directory of Open Access Journals (Sweden)

Radosavljević Slobodan A.

2016-01-01

Full Text Available Recent mineralogical, chemical, physical, and crystallographic investigations of the Boranja orefield showed very complex mineral associations and assemblages where sulfosalts have significant role. The sulfosalts of the Boranja orefield can be divided in four main groups: (i Pb-Sb(As-S system with ±Fe and ±Cu; (ii Cu(Ag-Fe(Zn-Sb(As-S system; (iii Ag(Pb-Bi(Sb-S; (iv and Pb-Bi-S(Te system. Spatially, these sulfosalts are widely spread, however, they are the most abundant in the following polymetallic deposits and ore zones: Cu(Bi-FeS Kram-Mlakva; Pb(Ag-Zn-FeS2 Veliki Majdan (Kolarica-Centralni revir-Kojići; Sb-Zn-Pb-As Rujevac; and Pb-Zn-FeS2-BaSO4 Bobija. The multi stage formation of minerals, from skarnhydrothermal to complex hydrothermal with various stages and sub-stages has been determined. All hydrothermal stages and sub-stages of various polymetallic deposits and ore zones within the Boranja orefield are followed by a variety of sulfosalts. [Projekat Ministarstva nauke Republike Srbije, br. OI-176016: Magmatism and geodynamics of the Balkan Peninsula from Mesozoic to present day: Significance for the formation of metallic and non-metallic mineral deposits

A review of silver-rich mineral deposits and their metallogeny

Science.gov (United States)

Graybeal, Frederick T.; Vikre, Peter

2010-01-01

Mineral deposits with large inventories or high grades of silver are found in four genetic groups: (1) volcanogenic massive sulfide (VMS), (2) sedimentary exhalative (SEDEX), (3) lithogene, and, (4) magmatichydrothermal. Principal differences between the four groups relate to source rocks and regions, metal associations, process and timing of mineralization, and tectonic setting. These four groups may be subdivided into specific metal associations on ternary diagrams based on relative metal contents. The VMS deposits rarely contain more than 15,600 t Ag (500 Moz). Grades average 33 g/t Ag. Variable Ag- Pb-Zn-Cu-Au ± Sn concentrations are interpreted as having been derived both from shallow plutons and by leaching of the volcanic rock pile in regions of thin or no continental crust and the mineralization is syngenetic. Higher silver grades are associated with areas of abundant felsic volcanic rocks. The SEDEX deposits rarely contain more than 15,600 t Ag (500 Moz). Grades average 46 g/t Ag. Silver, lead, and zinc in relatively consistent proportions are leached from sedimentary rocks filling rift-related basins, where the continental crust is thin, and deposited as syngenetic to diagenetic massive sulfides. Pre-mineral volcanic rocks and their detritus may occur deep within the basin and gold is typically absent. Lithogene silver-rich deposits are epigenetic products of varying combinations of compaction, dewatering, meteoric water recharge, and metamorphism of rift basin-related clastic sedimentary and interbedded volcanic rocks. Individual deposits may contain more than 15,600 t Ag (500 Moz) at high grades. Ores are characterized by four well-defined metal associations, including Ag, Ag-Pb-Zn, Ag-Cu, and Ag-Co-Ni-U. Leaching, transport, and deposition of metals may occur both in specific sedimentary strata and other rock types adjacent to the rift. Multiple mineralizing events lasting 10 to 15 m.y., separated by as much as 1 b.y., may occur in a single basin

Focused-ion-beam-fabricated Au nanorods coupled with Ag nanoparticles used as surface-enhanced Raman scattering-active substrate for analyzing trace melamine constituents in solution

International Nuclear Information System (INIS)

Sivashanmugan, Kundan; Liao, Jiunn-Der; Liu, Bernard Haochih; Yao, Chih-Kai

2013-01-01

Graphical abstract: -- Highlights: •Well-ordered Au-nanorod array with a controlled tip ring diameter (Au N Rs d ) is made by focused ion beam. •Au N Rs d coupled with Ag nanoparticles (Ag NPs/Au N Rs d ) is competent to sense target molecules in a solution. •Ag NPs/Au N Rs d SERS active substrate can detect a single molecule of crystal violet. •Ag NPs/Au N Rs d as a SERS-active substrate can distinguish melamine contaminants at low concentrations (e.g., 10 −12 M). -- Abstract: A well-ordered Au-nanorod array with a controlled tip ring diameter (Au N Rs d ) was fabricated using the focused ion beam method. Au N Rs d was then coupled with Ag nanoparticles (Ag NPs) to bridge the gaps among Au nanorods. The effect of surface-enhanced Raman scattering (SERS) on Au N Rs d and Ag NPs/Au N Rs d was particularly verified using crystal violet (CV) as the molecular probe. Raman intensity obtained from a characteristic peak of CV on Au N Rs d was estimated by an enhancement factor of ≈10 7 in magnitude, which increased ≈10 12 in magnitude for that on Ag NPs/Au N Rs d . A highly SERS-active Ag NPs/Au N Rs d was furthermore applied for the detection of melamine (MEL) at very low concentrations. Raman-active peaks of MEL (10 −3 to 10 −12 M) in water or milk solution upon Au N Rs d or Ag NPs/Au N Rs d were well distinguished. The peaks at 680 and 702 cm −1 for MEL molecules were found suitable to be used as the index for sensing low-concentration MEL in a varied solution, while that at 1051 cm −1 was practical to interpret MEL molecules in water or milk solution bonded with Au (i.e., Au N Rs d ) or Ag (i.e., Ag NPs/Au N Rs d ) surface. At the interface of Ag NPs/Au N Rs d and MEL molecules in milk solution, a laser-induced electromagnetic field or hotspot effect was produced and competent to sense low-concentration MEL molecules interacting with Ag and Au surfaces. Accordingly, Ag NPs/Au N Rs d is very promising to be used as a fast and sensitive tool for

Flexible nonvolatile memory devices based on Au/PMMA nanocomposites deposited on PEDOT:PSS/Ag nanowire hybrid electrodes

International Nuclear Information System (INIS)

Sung, Sihyun; Kim, Tae Whan

2017-01-01

Highlights: • Flexible nonvolatile memory (NVM) devices fabricated utilizing Au nanoparticles (AuNPs) embedded in a PMMA layer were fabricated. • The insertion of the PEDOT:PSS layer enhanced the surface uniformity of the AgNW bottom electrode, resulting in improved device performances. • Current-voltage curves for the Al/PMMA:AuNP/PEDOT:PSS/AgNW/PET devices showed clockwise current hysteresis behaviors. • ON/OFF ratio of 1 × 10 3 was maintained for retention times longer than 1 × 10 4 s. • Memory characteristics of the NVM devices before and after bending were similar. - Abstract: Flexible nonvolatile memory (NVM) devices fabricated utilizing Au nanoparticles (AuNPs) embedded in a poly(methylmethacrylate) (PMMA) layer were fabricated on a silver nanowire (AgNW) or a poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS)/AgNW coated on poly(ethylene terephthalate) (PET) substrates. The transmittance and the sheet resistance of the PEDOT:PSS/AgNW hybrid layer were approximately 89% and 50 Ω/sq, respectively, which were comparable to the values for commercial indium-tin-oxide (ITO) electrodes. Current-voltage curves for the Al/PMMA:AuNP/PEDOT:PSS/AgNW/PET devices at 300 K showed clockwise current hysteresis behaviors due to the existence of the AuNPs. The endurance number of ON/OFF switching for the NVM devices was above 30 cycles. An ON/OFF ratio of 1 × 10 3 was maintained for retention times longer than 1 × 10 4 s. The maximum memory margins of the NVM devices before and after bending were approximately 3.4 × 10 3 and 1.4 × 10 3 , respectively. The retention times of the devices before and after bending remained same 1 × 10 4 s. The memory margin and the stability of flexible NVMs fabricated on AgNW electrodes were enhanced due to the embedded PEDOT:PSS buffer layer.

Flexible nonvolatile memory devices based on Au/PMMA nanocomposites deposited on PEDOT:PSS/Ag nanowire hybrid electrodes

Energy Technology Data Exchange (ETDEWEB)

Sung, Sihyun; Kim, Tae Whan, E-mail: twk@hanyang.ac.kr

2017-07-31

Highlights: • Flexible nonvolatile memory (NVM) devices fabricated utilizing Au nanoparticles (AuNPs) embedded in a PMMA layer were fabricated. • The insertion of the PEDOT:PSS layer enhanced the surface uniformity of the AgNW bottom electrode, resulting in improved device performances. • Current-voltage curves for the Al/PMMA:AuNP/PEDOT:PSS/AgNW/PET devices showed clockwise current hysteresis behaviors. • ON/OFF ratio of 1 × 10{sup 3} was maintained for retention times longer than 1 × 10{sup 4} s. • Memory characteristics of the NVM devices before and after bending were similar. - Abstract: Flexible nonvolatile memory (NVM) devices fabricated utilizing Au nanoparticles (AuNPs) embedded in a poly(methylmethacrylate) (PMMA) layer were fabricated on a silver nanowire (AgNW) or a poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS)/AgNW coated on poly(ethylene terephthalate) (PET) substrates. The transmittance and the sheet resistance of the PEDOT:PSS/AgNW hybrid layer were approximately 89% and 50 Ω/sq, respectively, which were comparable to the values for commercial indium-tin-oxide (ITO) electrodes. Current-voltage curves for the Al/PMMA:AuNP/PEDOT:PSS/AgNW/PET devices at 300 K showed clockwise current hysteresis behaviors due to the existence of the AuNPs. The endurance number of ON/OFF switching for the NVM devices was above 30 cycles. An ON/OFF ratio of 1 × 10{sup 3} was maintained for retention times longer than 1 × 10{sup 4} s. The maximum memory margins of the NVM devices before and after bending were approximately 3.4 × 10{sup 3} and 1.4 × 10{sup 3}, respectively. The retention times of the devices before and after bending remained same 1 × 10{sup 4} s. The memory margin and the stability of flexible NVMs fabricated on AgNW electrodes were enhanced due to the embedded PEDOT:PSS buffer layer.

Pressure induced Ag{sub 2}Te polymorphs in conjunction with topological non trivial to metal transition

Energy Technology Data Exchange (ETDEWEB)

Zhu, J.; Zhang, S. J., E-mail: sjzhang@iphy.ac.cn, E-mail: jin@iphy.ac.cn; Yu, X. H.; Yu, R. C.; Jin, C. Q., E-mail: sjzhang@iphy.ac.cn, E-mail: jin@iphy.ac.cn; Dai, X.; Fang, Z. [Institute of Physics, Chinese Academy of Sciences, Beijing 100190 (China); Oganov, A. R. [Department of Geosciences, University of New York at Stony Brook (United States); Feng, W. X.; Yao, Y. G. [Department of Physics, Beijing Institute of Technology, Beijing (China); Zhu, J. L. [High Pressure Science and Engineering Center, University of Nevada, Las Vegas, Nevada 89154 (United States); Zhao, Y. S. [Institute of Physics, Chinese Academy of Sciences, Beijing 100190 (China); South University of Science and Technology of China, Shenzhen, Guangdong (China)

2016-08-15

Silver telluride (Ag{sub 2}Te) is well known as superionic conductor and topological insulator with polymorphs. Pressure induced three phase transitions in Ag{sub 2}Te have been reported in previous. Here, we experimentally identified high pressure phase above 13 GPa of Ag{sub 2}Te by using high pressure synchrotron x ray diffraction method in combination with evolutionary crystal structure prediction, showing it crystallizes into a monoclinic structure of space group C2/m with lattice parameters a = 6.081Å, b = 5.744Å, c = 6.797 Å, β = 105.53°. The electronic properties measurements of Ag{sub 2}Te reveal that the topologically non-trivial semiconducting phase I and semimetallic phase II previously predicated by theory transformed into bulk metals for high pressure phases in consistent with the first principles calculations.

AuScope research infrastructure - supporting Australian mineral discovery

Science.gov (United States)

McInnes, B.; Rawling, T.

2016-12-01

Earth and geospatial scientists are heavy users of data products. When industry geologists access spatial data from the field and the exploration office they require data products that are discoverable, searchable, interoperable and attributed with robust metadata. Over the last decade AuScope has utilised NCRIS funding to provide a variety of data products including geophysical data (reflection and passive seismic, magnetotellurics and gravity), GIS layers from state and national geological survey organisations, hyperspectral core logging (National Virtual Core Library) and time-series geospatial data from GNSS and VLBI instruments - all delivered using AuScope GRID technologies based on the Spatial Information Services Stack (SiSS). Perhaps one of the best examples of collaboration to deliver data products to industry users is the National Mineral Library. Working with researchers at Curtin Universities John de Laeter Centre and ANDS, AuScope has also supported the development of a Laboratory Information Management System (LIMS). The project has produced an entirely new workflow, based around a TESCAN TIMA field emission scanning electron microscope, that allows metadata to be collected and recorded from the sample collection and preparation right through to data delivery and publication. This process has facilitated the scanning of a large stockpile of mineral samples from across Western Australia that will produce a state-wide Mineral Library, allowing mineral explorers to better understand the composition of critical rock outcrop samples from all over the state. This new NCRIS supported initiative provides a dataset that underpins both academic and applied research programs and is important for the economic future of Australia. Mining companies do a lot of heavy mineral analysis in research and development but, because there isn't a baseline for mineralogy across each state, it is difficult to have full confidence in the heavy mineral data. This creates an

Molecular oxygen adsorption and dissociation on Au12M clusters with M = Cu, Ag or Ir

Science.gov (United States)

Jiménez-Díaz, Laura M.; Pérez, Luis A.

2018-03-01

In this work, we present a density functional theory study of the structural and electronic properties of isolated neutral clusters of the type Au12M, with M = Cu, Ag, or Ir. On the other hand, there is experimental evidence that gold-silver, gold-copper and gold-iridium nanoparticles have an enhanced catalytic activity for the CO oxidation reaction. In order to address these phenomena, we also performed density functional calculations of the adsorption and dissociation of O2 on these nanoparticles. Moreover, to understand the effects of Cu, Ag, and Ir impurity atoms on the dissociation of O2, we also analyze this reaction in the corresponding pure gold cluster. The results indicate that the substitution of one gold atom in a Au13 cluster by Ag, Cu or Ir diminishes the activation energy barrier for the O2 dissociation by nearly 1 eV. This energy barrier is similar for Au12Ag and Au12Cu, whereas for Au12Ir is even lower. These results suggest that the addition of other transition metal atoms to gold nanoclusters can enhance their catalytic activity towards the CO oxidation reaction, independently of the effect that the substrate could have on supported nanoclusters.

Mineral Deposit Data for Epigenetic Base- and Precious-metal and Uranium-thorium Deposits in South-central and Southwestern Montana and Southern and Central Idaho

Science.gov (United States)

Klein, T.L.

2004-01-01

Metal deposits spatially associated with the Cretaceous Boulder and Idaho batholiths of southwestern Montana and southern and central Idaho have been exploited since the early 1860s. Au was first discovered in placer deposits; exploitation of vein deposits in bedrock soon followed. In 1865, high-grade Ag vein deposits were discovered and remained economically important until the 1890s. Early high-grade deposits of Au, Ag and Pb were found in the weathered portions of the veins systems. As mining progressed to deeper levels, Ag and Pb grades diminished. Exploration for and development of these vein deposits in this area have continued until the present. A majority of these base- and precious-metal vein deposits are classified as polymetallic veins (PMV) and polymetallic carbonate-replacement (PMR) deposits in this compilation. Porphyry Cu and Mo, epithermal (Au, Ag, Hg and Sb), base- and precious-metal and W skarn, W vein, and U and Th vein deposits are also common in this area. The world-class Butte Cu porphyry and the Butte high-sulfidation Cu vein deposits are in this study area. PMV and PMR deposits are the most numerous in the region and constitute about 85% of the deposit records compiled. Several types of syngenetic/diagenetic sulfide mineral deposits in rocks of the Belt Supergroup or their equivalents are common in the region and they have been the source of a substantial metal production over the last century. These syngenetic deposits and their metamorphosed/structurally remobilized equivalents were not included in this database; therefore, deposits in the Idaho portion of the Coeur d'Alene district and the Idaho Cobalt belt, for example, have not been included because many of them are believed to be of this type.

c-T phase diagram and Landau free energies of (AgAu)55 nanoalloy via neural-network molecular dynamic simulations.

Science.gov (United States)

Chiriki, Siva; Jindal, Shweta; Bulusu, Satya S

2017-10-21

For understanding the structure, dynamics, and thermal stability of (AgAu) 55 nanoalloys, knowledge of the composition-temperature (c-T) phase diagram is essential due to the explicit dependence of properties on composition and temperature. Experimentally, generating the phase diagrams is very challenging, and therefore theoretical insight is necessary. We use an artificial neural network potential for (AgAu) 55 nanoalloys. Predicted global minimum structures for pure gold and gold rich compositions are lower in energy compared to previous reports by density functional theory. The present work based on c-T phase diagram, surface area, surface charge, probability of isomers, and Landau free energies supports the enhancement of catalytic property of Ag-Au nanoalloys by incorporation of Ag up to 24% by composition in Au nanoparticles as found experimentally. The phase diagram shows that there is a coexistence temperature range of 70 K for Ag 28 Au 27 compared to all other compositions. We propose the power spectrum coefficients derived from spherical harmonics as an order parameter to calculate Landau free energies.

Self-assembled monolayers of bimetallic Au/Ag nanospheres with superior surface-enhanced Raman scattering activity for ultra-sensitive triphenylmethane dyes detection.

Science.gov (United States)

Tian, Yue; Zhang, Hua; Xu, Linlin; Chen, Ming; Chen, Feng

2018-02-15

The bimetallic Au/Ag self-assembled monolayers (SAMs) were constructed by using mono-dispersed Au/Ag nanospheres (Ag: 4.07%-34.53%) via evaporation-based assembly strategy. The composition-dependent surface-enhanced Raman scattering (SERS) spectroscopy revealed that the Au/Ag (Ag: 16.83%) SAMs provide maximized activity for triphenylmethane dyes detection. With the inter-metallic synergy, the optimized SAMs enable the Raman intensity of crystal violet molecules to be about 223 times higher than that of monometallic Au SAMs. Moreover, the SERS signals with excellent uniformity (<5% variation) are sensitive down to 10 -13   M concentrations because of the optimal matching between bimetallic plasmon resonance and the incident laser wavelength.

Preparation of Au and Ag nanoparticles using Artemisia annua and their in vitro antibacterial and tyrosinase inhibitory activities

Energy Technology Data Exchange (ETDEWEB)

Basavegowda, Nagaraj; Idhayadhulla, Akber; Lee, Yong Rok, E-mail: yrlee@yu.ac.kr

2014-10-01

This work describes a plant-mediated approach to the preparation of metal nanoparticles using leaf extract of Artemisia annua (A. annua), an ethno-medicinal plant widely found in Asia, which was used as reducing and stabilizing agent. A. annua is used in traditional Chinese medicine to alleviate fever. Au and Ag nanoparticles were prepared using a one-step aqueous method at room temperature without any toxic chemicals. The formation of Au and Ag nanoparticles was monitored by UV–vis spectroscopy. Synthesized nanoparticles were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive X-ray analysis (EDX), Fourier transform infrared (FT-IR) spectroscopy, and thermogravimetric analysis (TGA). TEM analysis of Au nanoparticles showed that they had triangular and spherical shapes with sizes ranging from 15 to 40 nm. The silver nanoparticles were predominantly spherical and uniformly sized (30–50 nm). The Au and Ag nanoparticles produced showed significant tyrosinase inhibitory and antibacterial effects. These results suggest that the synthesized nanoparticles provide good alternatives in varied medical and industrial applications. - Highlights: • Au and Ag nanoparticles were synthesized using Artemisia annua leaf aqueous extract. • Nanoparticles were characterized by UV–vis spectroscopy, FT-IR, TEM, EDX, XRD, and TGA. • Au and Ag nanoparticles were of size 25 and 30 nm respectively, in spherical forms. • Nanoparticles showed significant tyrosinase inhibitory and antibacterial activities.

Preparation of Au and Ag nanoparticles using Artemisia annua and their in vitro antibacterial and tyrosinase inhibitory activities

International Nuclear Information System (INIS)

Basavegowda, Nagaraj; Idhayadhulla, Akber; Lee, Yong Rok

2014-01-01

This work describes a plant-mediated approach to the preparation of metal nanoparticles using leaf extract of Artemisia annua (A. annua), an ethno-medicinal plant widely found in Asia, which was used as reducing and stabilizing agent. A. annua is used in traditional Chinese medicine to alleviate fever. Au and Ag nanoparticles were prepared using a one-step aqueous method at room temperature without any toxic chemicals. The formation of Au and Ag nanoparticles was monitored by UV–vis spectroscopy. Synthesized nanoparticles were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive X-ray analysis (EDX), Fourier transform infrared (FT-IR) spectroscopy, and thermogravimetric analysis (TGA). TEM analysis of Au nanoparticles showed that they had triangular and spherical shapes with sizes ranging from 15 to 40 nm. The silver nanoparticles were predominantly spherical and uniformly sized (30–50 nm). The Au and Ag nanoparticles produced showed significant tyrosinase inhibitory and antibacterial effects. These results suggest that the synthesized nanoparticles provide good alternatives in varied medical and industrial applications. - Highlights: • Au and Ag nanoparticles were synthesized using Artemisia annua leaf aqueous extract. • Nanoparticles were characterized by UV–vis spectroscopy, FT-IR, TEM, EDX, XRD, and TGA. • Au and Ag nanoparticles were of size 25 and 30 nm respectively, in spherical forms. • Nanoparticles showed significant tyrosinase inhibitory and antibacterial activities

Focused-ion-beam-fabricated Au nanorods coupled with Ag nanoparticles used as surface-enhanced Raman scattering-active substrate for analyzing trace melamine constituents in solution

Energy Technology Data Exchange (ETDEWEB)

Sivashanmugan, Kundan [Department of Materials Science and Engineering, National Cheng Kung University, 1 University Road, Tainan 70101, Taiwan (China); Liao, Jiunn-Der, E-mail: jdliao@mail.ncku.edu.tw [Department of Materials Science and Engineering, National Cheng Kung University, 1 University Road, Tainan 70101, Taiwan (China); Center for Micro/Nano Science and Technology, National Cheng Kung University, 1 University Road, Tainan 70101, Taiwan (China); Liu, Bernard Haochih; Yao, Chih-Kai [Department of Materials Science and Engineering, National Cheng Kung University, 1 University Road, Tainan 70101, Taiwan (China)

2013-10-24

Graphical abstract: -- Highlights: •Well-ordered Au-nanorod array with a controlled tip ring diameter (Au{sub N}Rs{sub d}) is made by focused ion beam. •Au{sub N}Rs{sub d} coupled with Ag nanoparticles (Ag NPs/Au{sub N}Rs{sub d}) is competent to sense target molecules in a solution. •Ag NPs/Au{sub N}Rs{sub d} SERS active substrate can detect a single molecule of crystal violet. •Ag NPs/Au{sub N}Rs{sub d} as a SERS-active substrate can distinguish melamine contaminants at low concentrations (e.g., 10{sup −12} M). -- Abstract: A well-ordered Au-nanorod array with a controlled tip ring diameter (Au{sub N}Rs{sub d}) was fabricated using the focused ion beam method. Au{sub N}Rs{sub d} was then coupled with Ag nanoparticles (Ag NPs) to bridge the gaps among Au nanorods. The effect of surface-enhanced Raman scattering (SERS) on Au{sub N}Rs{sub d} and Ag NPs/Au{sub N}Rs{sub d} was particularly verified using crystal violet (CV) as the molecular probe. Raman intensity obtained from a characteristic peak of CV on Au{sub N}Rs{sub d} was estimated by an enhancement factor of ≈10{sup 7} in magnitude, which increased ≈10{sup 12} in magnitude for that on Ag NPs/Au{sub N}Rs{sub d}. A highly SERS-active Ag NPs/Au{sub N}Rs{sub d} was furthermore applied for the detection of melamine (MEL) at very low concentrations. Raman-active peaks of MEL (10{sup −3} to 10{sup −12} M) in water or milk solution upon Au{sub N}Rs{sub d} or Ag NPs/Au{sub N}Rs{sub d} were well distinguished. The peaks at 680 and 702 cm{sup −1} for MEL molecules were found suitable to be used as the index for sensing low-concentration MEL in a varied solution, while that at 1051 cm{sup −1} was practical to interpret MEL molecules in water or milk solution bonded with Au (i.e., Au{sub N}Rs{sub d}) or Ag (i.e., Ag NPs/Au{sub N}Rs{sub d}) surface. At the interface of Ag NPs/Au{sub N}Rs{sub d} and MEL molecules in milk solution, a laser-induced electromagnetic field or hotspot effect was produced and

Synthesis of unidirectional structures of SiO2-Ag using Au nanoparticles as nucleation centers

International Nuclear Information System (INIS)

Villa S, G.; Mendoza A, D.; Gutierrez W, C.; Perez H, R.

2008-01-01

This paper reports a method to synthesize Ag unidirectional structures covered with SiO 2 by sol-gel technique using Au nanoparticles as nucleation centers of the unidirectional structures. In the first phase unidirectional structures of SiO 2 -Ag CI are obtained by sol-gel, using TEOS as a precursor of metallic structures (Ag) and the incorporation of Au nanoparticles as nucleation centers for growth of unidirectional structures. In the second stage, one-way systems are subjected to thermal treatment in H 2 atmosphere for obtain AG 0 particles through mechanisms that diffusion and coalescence of silver to form structures that have a thin cover of SiO 2 . Analysis by scanning electron microscopy, transmission and atomic force microscopy allowed to determine the chemical composition and microstructural properties of unidirectional systems SiO 2 -Ag. (Author)

Controlled preparation of M(Ag, Au)/TiO2 through sulfydryl-assisted method for enhanced photocatalysis

Science.gov (United States)

Xia, Hongbo; Wu, Suli; Bi, Jiajie; Zhang, Shufen

2017-11-01

Here a simple and effective method was explored to fabricate M/TiO2 (M = Ag, Au) composites, which required neither pre-treatment of TiO2 nor any additives as reducing agent. Using amorphous TiO2 spheres functionalized with SH groups as starting materials, the noble metallic ions (Ag, Au) can be adsorbed by TiO2 due to their special affinity with SH groups, which is beneficial to the uniform dispersion of metallic ions on the surface of TiO2. Then the adsorbed ions were reduced to form noble metal nanoparticles by heating process (95 °C) directly without additive as reduction agent. Meanwhile, the amorphous TiO2 was transformed into anatase phase during the heating process. Thus, the transformation of TiO2 along with the reduction of noble metallic ions (Ag, Au) was simultaneously carried out by heating. The XRD patterns proved the formation of anatase TiO2 after heating. The characterizations of XPS and TEM proved the formation of Ag and Au nanoparticles on the surface of TiO2. The element mapping indicated that Ag nanoparticles are dispersed uniformly on the surface of TiO2. The photocatalytic activity of the composites has been investigated by the degradation of methyl orange under visible light irradiation. The results showed that when Ag/TiO2 (2.8 wt%) was used as photocatalyst, about 98% of the MO molecules were degraded in 70 min.

Bismuth-silver mineralization in the Sergozerskoe gold occurrence

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Kalinin A. A.

2017-03-01

Full Text Available Bismuth-silver mineralization attendant to gold mineralization in the Sergozerskoe gold occurrence has been studied in detail. Bi-Ag mineralization is connected with diorite porphyry dykes, which cut volcanic-sedimentary Lopian complexes of the Strel'ninsky greenstone belt – hornblendite and actinolite-chlorite amphibolites, biotite and bi-micaceous gneisses. Distribution of Bi-Ag mineralization similar to gold mineralization is controlled by 80 m thick zone of silicification. Bi minerals are found in brecciated diorite porphyry. Bismuth-silver mineralization includes native metals (bismuth, electrum, silver, tellurides (hedleyite, hessite, selenides (ikunolite, sulfides and sulfosalts of Bi and Ag (matildite, lillianite, eckerite, jalpaite, prustite, acanthite, a few undiagnosed minerals. All Bi and Ag minerals associate with galena. Composition of mineralization evolved from early to late stages of development, depending on intensity of rock alteration. The earliest Bi-Ag minerals were native bismuth and hedleyite formed dissemination in galena, and electrum with 30-45 mass.% Au. Later native bismuth was partly substituted by silver and bismuth sulfosalts and bismuth sulfides. The latest minerals were low-temperature silver sulfides eckerite, jalpaite, and acanthite, which were noted only in the most intensively altered rocks. As soon as the process of formation of Bi-Ag mineralization is the same as formation of gold, findings of bismuth-silver mineralization can serve as a positive exploration sign for gold in the region.

Biogenic synthesis of Ag-Au-In decorated on rGO nanosheet and its antioxidant and biological activities

Science.gov (United States)

Hazarika, Moushumi; Sonowal, Shashanka; Saikia, Indranirekha; Boruah, Purna K.; Das, Manash R.; Tamuly, Chandan

2017-09-01

Au-Ag-In-rGO nanocomposite was synthesized using fruit extract of Zanthoxylum rhetsa which is an eco-friendly, simple and green method. It was characterized by UV-visible, FT-IR, XRD, XPS, EDX, TEM technique. The antioxidant capacity of the nanocomposite was evaluated in presence of AgNO3, HAuCl4 and InCl3 solution respectively at 25 °C. The results showed significant antioxidant activity in presence of 1  ×  10-5 mM AgNO3 solution. The antibacterial activity of Au-Ag-In-rGO nanoparticles was carried out against the gram  -ve bacteria Pseudomonas aeruginosa, Escherichia coli and gram  +ve bacteria Staphylococcus aureus and Bacillus cereus. The bacterial growth kinetics was studied. The bacterial strain E. coli and S. aureus showed complete inhibition at concentration 100 µg ml-1. The activity is more effective in case of Au-Ag-In-rGO compared to GO.

Galvanic replacement-free deposition of Au on Ag for core-shell nanocubes with enhanced chemical stability and SERS activity.

Science.gov (United States)

Yang, Yin; Liu, Jingyue; Fu, Zheng-Wen; Qin, Dong

2014-06-11

We report a robust synthesis of Ag@Au core-shell nanocubes by directly depositing Au atoms on the surfaces of Ag nanocubes as conformal, ultrathin shells. Our success relies on the introduction of a strong reducing agent to compete with and thereby block the galvanic replacement between Ag and HAuCl4. An ultrathin Au shell of 0.6 nm thick was able to protect the Ag in the core in an oxidative environment. Significantly, the core-shell nanocubes exhibited surface plasmonic properties essentially identical to those of the original Ag nanocubes, while the SERS activity showed a 5.4-fold further enhancement owing to an improvement in chemical enhancement. The combination of excellent SERS activity and chemical stability may enable a variety of new applications.

Centrality and collision system dependence of antiproton production from p+A to Au+Au collisions at AGS energies

International Nuclear Information System (INIS)

Sako, H.; Ahle, L.; Akiba, Y.

1997-12-01

Antiproton production in heavy ion collisions reflects subtle interplay between initial production and absorption by nucleons. Because the AGS energies (10--20 A·GeV/c) are close to the antiproton production threshold, antiproton may be sensitive to cooperative processes such as QGP and hadronic multi-step processes. On the other hand, antiproton has been proposed as a probe of baryon density due to large N anti N annihilation cross sections. Cascade models predict the maximum baryon density reaches about 10 times the normal nucleus density in central Au+Au collisions, where the strong antiproton absorption is expected. In this paper, the authors show systematic studies of antiproton production from p+A to Au+Au collisions

Synthesis of Ag and Au nanoparticles embedded in carbon film: Optical, crystalline and topography analysis

Science.gov (United States)

Gholamali, Hediyeh; Shafiekhani, Azizollah; Darabi, Elham; Elahi, Seyed Mohammad

2018-03-01

Atomic force microscopy (AFM) images give valuable information about surface roughness of thin films based on the results of power spectral density (PSD) through the fast Fourier transform (FFT) algorithms. In the present work, AFM data are studied for silver and gold nanoparticles (Ag NPs a-C: H and Au NPs a-C: H) embedded in amorphous hydrogenated carbon films and co-deposited on glass substrate via of RF-Sputtering and RF-Plasma Enhanced Chemical Vapor Deposition methods. Here, the working gas is acetylene and the targets are Ag and Au. While time and power are constant, the only variable parameter in this study is initial pressure. In addition, the crystalline structure of Ag NPs a-C: H and Au NPs a-C: H are studied using X-ray diffraction (XRD). UV-visible spectrophotometry will also investigate optical properties and localized surface plasmon resonance (LSPR) of samples.

Influence of the additive Ag for crystallization of amorphous Ge-Sb-Te thin films

Energy Technology Data Exchange (ETDEWEB)

Song, Ki-Ho; Kim, Sung-Won; Seo, Jae-Hee [Faculty of Applied Chemical Engineering, Chonnam National University, 300 Yongbong-dong, Kwangju 500-757 (Korea, Republic of); Lee, Hyun-Yong, E-mail: hyleee@chonnam.ac.k [Faculty of Applied Chemical Engineering, Chonnam National University, 300 Yongbong-dong, Kwangju 500-757 (Korea, Republic of)

2009-05-29

We have investigated the optical and amorphous-to-crystalline transition properties in four-types of chalcogenide thin films; Ge{sub 2}Sb{sub 2}Te{sub 5}, Ge{sub 8}Sb{sub 2}Te{sub 11}, Ag-Ge{sub 2}Sb{sub 2}Te{sub 5} and Ag-Ge{sub 8}Sb{sub 2}Te{sub 11}. Crystallization was caused by nano-pulse illumination ({lambda} = 658 nm) with power (P) of 1-17 mW and pulse duration (t) of 10-460 ns, and the morphologies of crystallized spots were observed by SEM and microscope. It was found that the crystallized spot nearby linearly increases in size with increasing the illuminating energy (E = P {center_dot} t) and eventually ablated out by over illumination. Changes in the optical transmittance of as-deposited and annealed films were measured using a UV-vis-IR spectrophotometer. In addition, a speed of amorphous-to-crystalline transition was evaluated by detecting the reflection response signals for the nano-pulse scanning. Conclusively, the Ge{sub 8}Sb{sub 2}Te{sub 11} film has a faster crystallization speed than the Ge{sub 2}Sb{sub 2}Te{sub 5} film despite its higher crystallization temperature. The crystallization speed was largely improved by adding Ag in Ge{sub 2}Sb{sub 2}Te{sub 5} film but not in Ge{sub 8}Sb{sub 2}Te{sub 11} film. To explain these results, we considered a heat confinement by electron hopping.

Core–shell Au/Ag nanoparticles embedded in silicate sol–gel ...

Indian Academy of Sciences (India)

Administrator

Dedicated to the memory of the late Professor S K Rangarajan. *For correspondence. Core–shell Au/Ag nanoparticles embedded in silicate sol–gel network for sensor .... An immediate colour change was observed for the mixed solution, indicating the dis- persion of metal nanoparticles in the MTMOS sol– gel matrix.

Trace Elements and Minerals in Fumarolic Sulfur: The Case of Ebeko Volcano, Kuriles

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E. P. Shevko

2018-01-01

Full Text Available Native sulfur deposits on fumarolic fields at Ebeko volcano (Northern Kuriles, Russia are enriched in chalcophile elements (As-Sb-Se-Te-Hg-Cu and contain rare heavy metal sulfides (Ag2S, HgS, and CuS, native metal alloys (Au2Pd, and some other low-solubility minerals (CaWO4, BaSO4. Sulfur incrustations are impregnated with numerous particles of fresh and altered andesite groundmass and phenocrysts (pyroxene, magnetite as well as secondary minerals, such as opal, alunite, and abundant octahedral pyrite crystals. The comparison of elemental abundances in sulfur and unaltered rocks (andesite demonstrated that rock-forming elements (Ca, K, Fe, Mn, and Ti and other lithophile and chalcophile elements are mainly transported by fumarolic gas as aerosol particles, whereas semimetals (As, Sb, Se, and Te, halogens (Br and I, and Hg are likely transported as volatile species, even at temperatures slightly above 100°C. The presence of rare sulfides (Ag2S, CuS, and HgS together with abundant FeS2 in low-temperature fumarolic environments can be explained by the hydrochloric leaching of rock particles followed by the precipitation of low-solubility sulfides induced by the reaction of acid solutions with H2S at ambient temperatures. The elemental composition of native sulfur can be used to qualitatively estimate elemental abundances in low-temperature fumarolic gases.

Local order origin of thermal stability enhancement in amorphous Ag doping GeTe

Energy Technology Data Exchange (ETDEWEB)

Xu, L.; Li, Y.; Yu, N. N.; Zhong, Y. P.; Miao, X. S., E-mail: miaoxs@mail.hust.edu.cn [Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology (HUST), Wuhan 430074 (China); School of Optical and Electronic Information, Huazhong University of Science and Technology, Wuhan 430074 (China)

2015-01-19

We demonstrate the impacts of Ag doping on the local atomic structure of amorphous GeTe phase-change material. The variations of phonon vibrational modes, boding nature, and atomic structure are shown by Raman, X-ray photoelectron spectroscopy, and ab initio calculation. Combining the experiments and simulations, we observe that the number of Ge atoms in octahedral site decreases and that in tetrahedral site increases. This modification in local order of GeTe originating from the low valence element will affect the crystallization behavior of amorphous GeTe, which is verified by differential scanning calorimetry and transmission electron microscope results. This work not only gives the analysis on the structural change of GeTe with Ag dopants but also provides a method to enhance the thermal stability of amorphous phase-change materials for memory and brain-inspired computing applications.

Geology of epithermal silver-gold bulk-mining targets, bodie district, Mono County, California

Science.gov (United States)

Hollister, V.F.; Silberman, M.L.

1995-01-01

The Bodie mining district in Mono County, California, is zoned with a core polymetallic-quartz vein system and silver- and gold-bearing quartz-adularia veins north and south of the core. The veins formed as a result of repeated normal faulting during doming shortly after extrusion of felsic flows and tuffs, and the magmatic-hydrothermal event seems to span at least 2 Ma. Epithermal mineralization accompanied repeated movement of the normal faults, resulting in vein development in the planes of the faults. The veins occur in a very large area of argillic alteration. Individual mineralized structures commonly formed new fracture planes during separate fault movements, with resulting broad zones of veinlets growing in the walls of the major vein-faults. The veinlet swarms have been found to constitute a target estimated at 75,000,000 tons, averaging 0.037 ounce gold per ton. The target is amenable to bulkmining exploitation. The epithermal mineralogy is simple, with electrum being the most important precious metal mineral. The host veins are typical low-sulfide banded epithermal quartz and adularia structures that filled voids created by the faulting. Historical data show that beneficiation of the simple vein mineralogy is very efficient. ?? 1995 Oxford University Press.

Fabrication of Au/graphene oxide/Ag sandwich structure thin film and its tunable energetics and tailorable optical properties

Directory of Open Access Journals (Sweden)

Ruijin Hong

2017-01-01

Full Text Available Au/graphene oxide/Ag sandwich structure thin film was fabricated. The effects of graphene oxide (GO and bimetal on the structure and optical properties of metal silver films were investigated by X-ray diffraction (XRD, optical absorption, and Raman intensity measurements, respectively. Compared to silver thin film, Au/graphene oxide/Ag sandwich structure composite thin films were observed with wider optical absorption peak and enhanced absorption intensity. The Raman signal for Rhodamine B molecules based on the Au/graphene oxide/Ag sandwich nanostructure substrate were obviously enhanced due to the bimetal layer and GO layer with tunable absorption intensity and fluorescence quenching effects.

Characteristics of Al/p-AgGaTe2 polycrystalline thin film Schottky barrier diode

International Nuclear Information System (INIS)

Patel, S.S.; Patel, B.H.; Patel, T.S.

2008-01-01

An Al/p-AgGaTe 2 polycrystalline thin film schottky barrier diode have been prepared by flash-evaporation of p-AgGaTe 2 onto a pre-deposited film of aluminium. The current-voltage, capacitance-voltage and photoresponse of the diode have been investigated. The important physical parameter such as barrier height of the fabricated diode was derived from these measurements. (copyright 2008 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

Evolution of local structure in Ag2O-TeO2 glasses with addition of Ag2O analyzed by pulsed neutron diffraction and Raman spectroscopy

International Nuclear Information System (INIS)

Iwadate, Yasuhiko; Suzuki, Mineta; Hattori, Takeo; Fukushima, Kazuko; Nishiyama, Shin; Misawa, Masakatsu; Fukunaga, Toshiharu; Itoh, Keiji

2005-01-01

The local structure of Ag 2 O-TeO 2 glasses was studied by time-of-flight pulsed neutron diffraction (TOF-PND) and Raman spectroscopy. The results of Raman spectroscopy indicated that TeO 4 trigonal bipyramidal units (tbp) were converted to TeO 3 trigonal pyramidal units (tp) by addition of Ag 2 O to TeO 2 . Furthermore in PND, the structural parameters for each atomic pair were optimized in the Q-space, and the distances of the near neighbor Te-O correlations forming tbp units and tp units in the network were estimated with some accuracy

Fabrication and characterization of Au/n-CdTe Schottky barrier under illumination and dark

Science.gov (United States)

Bera, Swades Ranjan; Saha, Satyajit

2018-04-01

CdTe nanoparticles have been grown by chemical reduction method using EDA as capping agent. These are used to fabricate Schottky barrier in a simple cost-effective way at room temperature. The grown nanoparticles are structurally characterized by X-ray diffraction (XRD), Transmission electron microscopy (TEM). The optical properties of nano CdTe is characterized by UV-Vis absorption spectra, PL spectra. The band gap of the CdTe nanoparticles is increased as compared to CdTe bulk form indicating there is blue shift. The increase of band gap is due to quantum confinement. Photoluminescence spectra shows peak which corresponds to emission from surface state. CdTe nanofilm is grown on ITO coated glass substrate by dipping it on toluene containing dispersed CdTe nanoparticles. Schottky barrier of Au/n-CdTe is fabricated on ITO coated glass by vacuum deposition of gold. I- V and C- V characteristics of Au/n-CdTe Schottky barrier junction have been studied under dark and light condition. It is found that these characteristics are influenced by surface or interface traps. The values of barrier height, ideality factor, donor concentration and series resistance are obtained from the reverse bias capacitance-voltage measurements.

Structural characterization of AgGaTe{sub 2} layers grown on a- and c-sapphire substrates by a closed space sublimation method

Energy Technology Data Exchange (ETDEWEB)

Uruno, Aya; Usui, Ayaka [Department of Electrical Engineering and Bioscience, Waseda University, 3-4-1 Okubo, Shinjuku, Tokyo 169-8555 (Japan); Kobayashi, Masakazu [Department of Electrical Engineering and Bioscience, Waseda University, 3-4-1 Okubo, Shinjuku, Tokyo 169-8555 (Japan); Kagami Memorial Research Institute for Materials Science and Technology, Waseda University, 2-8-26 Nishiwaseda, Shinjuku, Tokyo 169-0051 (Japan)

2014-07-15

AgGaTe{sub 2} layers were grown on a- and c-plane sapphire substrates by a closed space sublimation method with varying the source temperature. Grown films were evaluated by θ -2θ and pole figure measurements of X-ray diffraction. AgGaTe{sub 2} layers were grown to have strong preference for the (103) orientation. However, it was cleared the Ag{sub 5}Te{sub 3} was formed along with the AgGaTe{sub 2} when the layer was grown on c-plane sapphire. The orientation of the film was analyzed by using the pole figure, and resulted in AgGaTe{sub 2} without Ag{sub 5}Te{sub 3} layers could be grown on a-plane sapphire. (copyright 2014 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

Topological description of mechanical behavior of Cu, Ag and Au: A first-principle study

Directory of Open Access Journals (Sweden)

M Saghayezhian

2011-12-01

Full Text Available  Mechanical properties and stress-strain curves of Cu, Ag and Au single crystals are calculated using ab initio methods. Elastic and Plastic regions are scrutinized. Yield stress and slope of these curves can shed light on brittlenesss and ductility of these metals that prove Cu, despite its high ultimate tensile strength, is less ductile than Au and Ag. Analysis of topology of charge density along with stress-strain curves shows that the elastic-plastic transition accompanies topological transition and for these metals, both transitions occur in the same strain. Some charactristics of critical point, especially bond points, are inspected.

Age-hardening and related phase transformation in an experimental Ag-Cu-Pd-Au alloy

International Nuclear Information System (INIS)

Seol, Hyo-Joung; Lee, Doung-Hun; Lee, Hee-Kyung; Takada, Yukyo; Okuno, Osamu; Kwon, Yong Hoon; Kim, Hyung-Il

2006-01-01

The age-hardening behaviour, phase transformation and related microstructural changes of an experimental Ag-Cu-Pd-Au alloy were examined by means of hardness test, X-ray diffraction (XRD), scanning electron microscopic (SEM) observations and electron probe microanalysis (EPMA). The specimen alloy showed apparent age-hardenability at the aging temperatures of 350 deg. C and 400 deg. C. By aging the solution-treated specimen at 400 deg. C, two phases of the Ag-rich α 1 phase and the Pd-containing Cu-rich α 2 phase were transformed into four phases of the Ag-rich α 1 ' phase, the Cu-rich α 2 ' phase, the CsCl-type CuPd phase and the AuCu(I) ordered phase. Microstructure of the solution-treated specimen consisted of the Ag-rich α 1 matrix, Cu-rich α 2 particle-like structures of various sizes and the lamellar structure of the α 1 and α 2 phases. When the peak hardness was obtained, the very fine lamellar structure consisting of the Ag-rich α 1 ' and Cu-rich α 2 ' phases was newly formed in the matrix. By further aging, the very fine lamellar structure grew and coarsened apparently, and the matrix was covered with the coarsened lamellar structure. The hardness increase was considered to be caused mainly by the diffusion and precipitation of Cu from the Ag-rich α 1 matrix, and the hardness decrease in the latter stage of age-hardening process was caused by the coarsening of the very fine lamellar structure. The CsCl-type CuPd phase and the AuCu(I) ordered phase did not contribute to the hardness increase

Geology, alteration, mineralization, petrogenesis, geochronology, geochemistry and airborne geophysics of Kuh Shah prospecting area, SW Birjand

Directory of Open Access Journals (Sweden)

Maryam Abdi

2012-04-01

Full Text Available The Kuh Shah prospecting area is located in Tertiary volcano-plutonic belt of the Lut Block. More than seventeen subvolcanic intermediate to acidic intrusive rocks, diorite to syenite in composition, were identified in the study area. The intrusions are related to hydrothermal alteration zones and contain argillic, propylitic, advanced argillic, silicified, quartz-sericite-pyrite, gossan and hydrothermal breccia which overprinted to each other and are accompanied by weathering which made it complicated to distinguish zoning. Mineralization is observed as sulfide (pyrite and rare chalcopyrite, disseminated Fe-oxides and quartz-Fe-oxide stockwork veinlets. Intrusive rocks are metaluminous, calc-alkaline with shoshonitic affinity with high values of magnetic susceptibility. The Kuh Shah intrusive rocks are classified as magnetite-series of oxidant I-type granitoids. Based on zircon U–Pb age dating, the age of these granitoid rocks is 39.7± 0.7 Ma (Middle Eocene. The radioisotope data (initial 87Sr/86Sr and 143Nd/144Nd ratios as well as εNd and geochemical data suggest that the Kuh Shah granitoid rocks formed from depleted mantle in a subduction-related magmatic arc setting. Geochemical anomalies of elements such as Cu, Au, Fe, Pb, Zn, As, Sb, Mo, Bi, Hg and also Mn, Ba, Te and Se, correlated with quartz-sericite-pyrite, gossan-stockwork-hydrothermal breccias, irregular silicified bodies and advanced argillic hydrothermal alteration zones. Geophysical anomalies correlated with hydrothermal alteration and mineralization zones. The interpretation of the results represents complex patterns of sub-circular to ellipsoid shape with north-east to south-west direction. These evidences are similar to the other for known Cu-Au porphyry and Au-epithermal systems in Iran and worldwide.

Charge-state distribution in close collisions of 3 MeV C2+ ions with Ag and Au atoms

NARCIS (Netherlands)

Boerma, D.O; Arnoldbik, W.M.; Kabachnik, N.M.; Khodyrev, V.A.

The charge-state distributions of 3 MeV carbon ions scattered over angles of 40 degrees and 60 degrees from sub-monolayers of Ag and Au atoms evaporated on a substrate and from thick layers of Ag and Au have been measured. A close similarity of the charge distributions in all cases is interpreted as

Wavelength feature mapping as a proxy to mineral chemistry for investigating geologic systems: An example from the Rodalquilar epithermal system

Science.gov (United States)

van der Meer, Freek; Kopačková, Veronika; Koucká, Lucie; van der Werff, Harald M. A.; van Ruitenbeek, Frank J. A.; Bakker, Wim H.

2018-02-01

The final product of a geologic remote sensing data analysis using multi spectral and hyperspectral images is a mineral (abundance) map. Multispectral data, such as ASTER, Landsat, SPOT, Sentinel-2, typically allow to determine qualitative estimates of what minerals are in a pixel, while hyperspectral data allow to quantify this. As input to most image classification or spectral processing approach, endmembers are required. An alternative approach to classification is to derive absorption feature characteristics such as the wavelength position of the deepest absorption, depth of the absorption and symmetry of the absorption feature from hyperspectral data. Two approaches are presented, tested and compared in this paper: the 'Wavelength Mapper' and the 'QuanTools'. Although these algorithms use a different mathematical solution to derive absorption feature wavelength and depth, and use different image post-processing, the results are consistent, comparable and reproducible. The wavelength images can be directly linked to mineral type and abundance, but more importantly also to mineral chemical composition and subtle changes thereof. This in turn allows to interpret hyperspectral data in terms of mineral chemistry changes which is a proxy to pressure-temperature of formation of minerals. We show the case of the Rodalquilar epithermal system of the southern Spanish Gabo de Gata volcanic area using HyMAP airborne hyperspectral images.

Localized surface plasmon resonance properties of symmetry-broken Au-ITO-Ag multilayered nanoshells

Science.gov (United States)

Lv, Jingwei; Mu, Haiwei; Lu, Xili; Liu, Qiang; Liu, Chao; Sun, Tao; Chu, Paul K.

2018-06-01

The plasmonic properties of symmetry-broken Au-ITO-Ag multilayered nanoshells by shell cutting are studied by the finite element method. The influence of the polarization of incident light and geometrical parameters on the plasmon resonances of the multilayered nanoshells are investigated. The polarization-dependent multiple plasmon resonances appear from the multilayered nanoshells due to symmetry breaking. In nanostructures with a broken symmetry, the localized surface plasmon resonance modes are enhanced resulting in higher order resonances. According to the plasmon hybridization theory, these resonance modes and greater spectral tunability derive from the interactions of an admixture of both primitive and multipolar modes between the inner Au core and outer Ag shell. By changing the radius of the Au core, the extinction resonance modes of the multilayered nanoshells can be easily tuned to the near-infrared region. To elucidate the symmetry-broken effects of multilayered nanoshells, we link the geometrical asymmetry to the asymmetrical distributions of surface charges and demonstrate dipolar and higher order plasmon modes with large associated field enhancements at the edge of the Ag rim. The spectral tunability of the multiple resonance modes from visible to near-infrared is investigated and the unique properties are attractive to applications including angularly selective filtering to biosensing.

The Chahnaly low sulfidation epithermal gold deposit, western Makran volcanic arc, southeastern Iran

Science.gov (United States)

Sholeh, Ali; Rastad, Ebrahim; Huston, David L.; Gemmell, J. Bruce; Taylor, Ryan D.

2016-01-01

The Chahnaly low-sulfidation epithermal Au deposit and nearby Au prospects are located northwest of the intermittently active Bazman stratovolcano on the western end of the Makran volcanic arc, which formed as the result of subduction of the remnant Neo-Tethyan oceanic crust beneath the Lut block. The arc hosts the Siah Jangal epithermal and Kharestan porphyry prospects, near Taftan volcano, as well as the Saindak Cu-Au porphyry deposit and world-class Reko Diq Cu-Au porphyry deposit, near Koh-i-Sultan volcano to the east-northeast in Pakistan. The host rocks for the Chahnaly deposit include early Miocene andesite and andesitic volcaniclastic rocks that are intruded by younger dacitic domes. Unaltered late Miocene dacitic ignimbrites overlie these rocks. Laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) U-Pb zircon geochronology data yield ages between 21.8 and 9.9 Ma for the acidic-intermediate regional volcanism. The most recent volcanic activity of the Bazman stratovolcano involved extrusion of an olivine basalt during Pliocene to Quaternary times. Interpretation of geochemical data indicate that the volcanic rocks are synsubduction and calc-alkaline to subalkaline. The lack of a significant negative Eu anomaly, a listric-shaped rare earth element pattern, and moderate La/Yb ratios of host suites indicate a high water content of the source magma.

Planar potentiometric sensors based on Au and Ag microelectrodes and conducting polymers for flow-cell analysis

International Nuclear Information System (INIS)

ToczyIowska, Renata; Pokrop, RafaI; Dybko, Artur; Wroblewski, Wojciech

2005-01-01

Back-side contact Au and Ag microelectrodes were used as transducers to construct planar all-solid-state electrodes suitable for flow-through analysis. The microsensors were based on plasticized PVC potassium-selective membranes containing ion-electron conducting polymer-polypyrrole doped with di(2-ethylhexyl) sulfosuccinate. The proposed technique allowed simple construction of microsensors in one step, by membrane solution casting directly on the surface of the planar metallic transducers. The performance of the microsensors based on Au and Ag transducers were determined and compared with planar sensors based on internal electrolyte immobilized in polyHEMA. The addition of the polypyrrole to the membrane composition did not influence on the selectivity, reproducibility and long-term stability of the microsensors but improved their standard potential stability in time in comparison with coated-wire type sensors. Moreover, all-solid-state microsensors based on Au transducers exhibited better signal stability than Ag based sensors

Epithermal beam development at the BMRR [Brookhaven Medical Research Reactor]: Dosimetric evaluation

International Nuclear Information System (INIS)

Saraf, S.K.; Fairchild, R.G.; Kalef-Ezra, J.; Laster, B.H.; Fiarman, S.; Ramsey, E.; Ioannina Univ.; Brookhaven National Lab., Upton, NY; State Univ. of New York, Stony Brook, NY

1989-01-01

The utilization of an epithermal neutron beam for neutron capture therapy (NCT) is desirable because of the increased tissue penetration relative to a thermal neutron beam. Over the past few years, modifications have been and continue to be made at the Brookhaven Medical Research Reactor (BMRR) by changing its filter components to produce an optimal epithermal beam. An optimal epithermal beam should contain a low fast neutron contamination and no thermal neutrons in the incident beam. Recently a new moderator for the epithermal beam has been installed at the epithermal port of the BMRR and has accomplished this task. This new moderator is a combination of alumina (Al 2 O 3 ) bricks and aluminum (Al) plates. A 0.51 mm thick cadmium (Cd) sheet has reduced the thermal neutron intensity drastically. Furthermore, an 11.5 cm thick bismuth (Bi) plate installed at the port surface has reduced the gamma dose component to negligible levels. Foil activation techniques have been employed by using bare gold and cadmium-covered gold foil to determine thermal as well as epithermal neutron fluence. Fast neutron fluence has been determined by indium foil counting. Fast neutron and gamma dose in soft tissue, free in air, is being determined by the paired ionization chamber technique, using tissue equivalent (TE) and graphite chambers. Thermoluminescent dosimeters (TLD-700) have also been used to determine the gamma dose independently. This paper describes the methods involved in the measurements of the above mentioned parameters. Formulations have been developed and the various corrections involved have been detailed. 12 refs

Fe-U-PGE-Au-Ag-Cu Deposits of the Udokan-Chiney Region (East Siberia, Russia)

Science.gov (United States)

Gongalskiy, B.; Krivolutskaya, N.; Murashov, K.; Nistratov, S.; Gryazev, S.

2012-04-01

Introduction. Cupriferous sandstones-shales and magmatic copper-nickel deposits mark out the western and southern boundaries of the Siberian Craton accordingly. Of special interest are the Paleoproterozoic deposits of the Udokan-Chiney mining district (Gongalskiy, Krivolutskaya, 2008). Copper reserves and resources of this region are estimated at more than 50 Mt. Half of them is concentrated at the unique Udokan Deposit and the second half is distributed among sedimentary (Unkur, Pravoingamakitskoye, Sakinskoye, Krasnoye, Burpala) and magmatic deposits of the Chiney (Rudnoye, Verkhnechineyskoye, Kontaktovoye), Luktur and Maylav massifs. Results. It was established that the ores are characterized by similarity in chemical composition (main, major and rare elements that are Ag, Au, PGE) and mineral assemblages with varying proportions. It is important to emphasize that Fe role in mineralization was previously ignored. Meanwhile the Udokan deposit contains 10 Mt of magnetite metacrystals so as chalcocite ores may contain up to 50% magnetite too. It has been recently found that the Chiney titanomagnetite ores comprise commercially significant uranium and rare-earth metal concentrations (Makaryev et al., 2011). Thus the Udokan-Chiney region comprises Cu, Fe, Ti, V, U, REE, Ag, Au, PGE. These deposits differ from similar objects, the Olympic Dam in particular, by a much smaller content of fluid-bearing minerals. Copper mineralization at the Udokan is represented by chalcocite-bornite ores. They occur as ore beds conformable with sedimentary structures or as cross-cutting veins. The central zones of the former are often brecciated. They are rimmed by fine magnetite, bornite, and chalcocite dissemination. Bornite-chalcopyrite and chalcopyrite-pyrite veins are known at the lower levels of the Udokan ore bed. Such ore compositions are predominant in other ore deposits in sedimentary rocks (Pravoingamakitskoye, Unkur) and have a hydrothermal origin. Silver grades are up to

130 MeV Au ion irradiation induced dewetting on In2Te3 thin film

International Nuclear Information System (INIS)

Matheswaran, P.; Abhirami, K.M.; Gokul, B.; Sathyamoorthy, R.; Prakash, Jai; Asokan, K.; Kanjilal, D.

2012-01-01

Highlights: ► In 2 Te 3 phase formed from In/Te bilayer by 130 MeV Au ion irradiation. ► Lower fluence results mixed phases with initial state of dewetting. ► At higher fluence, In 2 Te 3 phase with complete dewetting pattern is formed. ► Thermal spike model is used to explain the inter face mixing phenomena. ► SHI irradiation may be used to functionalize the structural and surface properties of thin films. - Abstract: In/Te bilayer thin films were prepared by sequential thermal evaporation and subsequently irradiated by 130 MeV Au ions. The pristine and irradiated samples were characterized by X-ray diffraction (XRD), Rutherford backscattering spectrometry (RBS), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX) techniques. RBS spectra reveal the sputtering of Te film and interface mixing, with increasing fluence. The surface morphology showed the beginning of dewetting of Te thin film and formation of the partially connected with the mixed zones at the fluence of 1 × 10 13 ions/cm 2 . At the higher fluence of 3 × 10 13 ions/cm 2 , dewetted structures were isolated at the surface. Above results are explained based on the formation of craters, sputtering and dewetting followed by inter-diffusion at the interface of molten zones due to thermal spike induced by Au ions.

Diffusion of Ag, Au and Cs implants in MAX phase Ti3SiC2

Energy Technology Data Exchange (ETDEWEB)

Jiang, Weilin; Henager, Charles H.; Varga, Tamas; Jung, Hee Joon; Overman, Nicole R.; Zhang, Chonghong; Gou, Jie

2015-05-16

MAX phases (M: early transition metal; A: elements in group 13 or 14; X: C or N), such as titanium silicon carbide (Ti3SiC2), have a unique combination of both metallic and ceramic properties, which make them attractive for potential nuclear applications. Ti3SiC2 has been considered as a possible fuel cladding material. This study reports on the diffusivities of fission product surrogates (Ag and Cs) and a noble metal Au (with diffusion behavior similar to Ag) in this ternary compound at elevated temperatures, as well as in dual-phase nanocomposite of Ti3SiC2/3C-SiC and polycrystalline CVD 3C-SiC for behavior comparisons. Samples were implanted with Ag, Au or Cs ions and characterized with various methods, including x-ray diffraction, electron backscatter diffraction, energy dispersive x-ray spectroscopy, Rutherford backscattering spectrometry, helium ion microscopy, and transmission electron microscopy. The results show that in contrast to immobile Ag in 3C-SiC, there is a significant outward diffusion of Ag in Ti3SiC2 within the dual-phase nanocomposite during Ag ion implantation at 873 K. Similar behavior of Au in polycrystalline Ti3SiC2 was also observed. Cs out-diffusion and release from Ti3SiC2 occurred during post-implantation thermal annealing at 973 K. This study suggests caution and further studies in consideration of Ti3SiC2 as a fuel cladding material for advanced nuclear reactors operating at very high temperatures.

Diffusion of single Au, Ag and Cu atoms inside Si(111)-(7 × 7) half unit cells: A comparative study

Energy Technology Data Exchange (ETDEWEB)

Liu, Qin [Department of Physics, Southern University of Science and Technology, Shenzhen, Guangdong 518055 (China); Department of Physics, The Chinese University of Hong Kong, Shatin, New Territory, Hong Kong (China); Science and Technology on Surface Physics and Chemistry Laboratory, Mianyang, Sichuan 621908 (China); Fu, Qiang [Institut für Physik and IRIS Adlershof, Humboldt-Universität zu Berlin, Zum Großen Windkanal 6, 12489 Berlin (Germany); Shao, Xiji; Ma, Xuhang; Wu, Xuefeng [Department of Physics, Southern University of Science and Technology, Shenzhen, Guangdong 518055 (China); Wang, Kedong, E-mail: wangkd@sustc.edu.cn [Department of Physics, Southern University of Science and Technology, Shenzhen, Guangdong 518055 (China); Xiao, Xudong, E-mail: xdxiao@phy.cuhk.edu.hk [Department of Physics, The Chinese University of Hong Kong, Shatin, New Territory, Hong Kong (China)

2017-04-15

Highlights: • Diffusions of Au, Ag and Cu atoms in the half unit cells of Si(111)-(7×7) have been studied by using a STM-based I-t method. • Despite their similar absorption sites, the diffusion dynamics show obvious differences between Ag and the other two. • Theoretical calculations suggest that different potential energy profiles are responsible for the observed differences. - Abstract: The diffusion behaviors of single Au, Ag and Cu atoms on Si(111)-(7 × 7) half unit cells have been investigated via combining scanning tunneling microscopy and first-principles calculations. Despite the similar adsorption sites between both half unit cells among these elements, the diffusion dynamics show obvious differences between Ag and the other two. Although obvious asymmetry has been found in the diffusion behaviors of Au and Cu atoms in two half unit cells of Si(111)-(7 × 7), the asymmetry behaves in a way different from that of Ag atoms and no dual-time character has been observed for the diffusions of Au and Cu in both half unit cells. Theoretical calculations suggest a different potential energy profile caused by the stronger hybridization between d states of Au (Cu) and Si states make the concept of basin useless for the diffusion of Au and Cu atoms inside the half unit cells of Si(111)-(7 × 7).

Intervention intégrée quant au risque de diabète après le diabète ...

International Development Research Centre (IDRC) Digital Library (Canada)

Les femmes ayant souffert de diabète sucré de la grossesse, un diabète temporaire qui apparaît pendant la grossesse, présentent un risque élevé de développer le diabète de type 2 après leur grossesse. Cette étude de recherche abordera le problème en Afrique du Sud par l'intermédiaire d'une intervention novatrice au ...

Direct flow in 10.8 GeV/nucleon Au+Au collisions measured in experiment E917 at the AGS

International Nuclear Information System (INIS)

Back, B. B.; Betts, R. R.; Britt, H. C.; Chang, J.; Chang, W. C.; Gillitzer, A.; Henning, W. F.; Hofman, D. J.; Nanal, V.; Wuosmaa, A. H.

1999-01-01

Analysis of directed flow observable for protons and pions from Au+Au collisions at 10.8 GeV/nucleon from experiment E917 at the AGS is presented. Using a Fourier series expansion, the first Fourier component, ν 1 ,was extracted as a function of rapidity for mid-central collisions (17-24%). Clear evidence for positive directed flow is found in the proton data, and a weak, possibly negative directed flow signal is observed for π + and π -

Hardening mechanism of an Ag-Pd-Cu-Au dental casting alloy

International Nuclear Information System (INIS)

Seol, Hyo-Joung; Kim, Gi-Chul; Son, Kuk-Hyeon; Kwon, Yong Hoon; Kim, Hyung-Il

2005-01-01

Age-hardening behaviour and the related microstructural changes were studied to elucidate the hardening mechanism of an Ag-Pd-Cu-Au dental casting alloy by means of hardness test, X-ray diffraction (XRD), scanning electron microscopic (SEM) observations and electron probe microanalysis (EPMA). By considering hardness test and XRD results together, it was revealed that the hardness increased during the early stage of phase transformation of α into α 1 . In the SEM photographs, two phases of matrix and particle-like structures were observed, and the precipitation of element from the matrix progressed during isothermal aging. By SEM observations and EPMA analysis, it could be supposed that the increase in hardness was caused by the diffusion and aggregation of Cu atoms from the Ag-rich α matrix containing Au and Cu in the early stage of age-hardening process, and that the decrease in hardness was caused by the progress of coarsening of Cu-rich lamellar precipitates in the later stage of the age-hardening process. The changes in the Ag-rich matrix caused both the increase and decrease in hardness, and the CuPd phase containing small amounts of Zn and Sn did not contribute to the hardness changes

Age-hardening and related phase transformation in an experimental Ag-Cu-Pd-Au alloy

Energy Technology Data Exchange (ETDEWEB)

Seol, Hyo-Joung [Department of Dental Materials, College of Dentistry, Pusan National University, 1-10 Ami-dong, Seo-gu, Pusan 602-739 (Korea, Republic of); Lee, Doung-Hun [Department of Dental Materials, College of Dentistry, Pusan National University, 1-10 Ami-dong, Seo-gu, Pusan 602-739 (Korea, Republic of); Lee, Hee-Kyung [Department of Dental Technology, Daegu Health College, San 7 Taejeon-dong, Buk-gu, Daegu 702-722 (Korea, Republic of); Takada, Yukyo [Division of Dental Biomaterials, Graduate School of Dentistry, Tohoku University, 4-1 Seiryo-machi, Aoba-ku, Sendai 980-8575 (Japan); Okuno, Osamu [Division of Dental Biomaterials, Graduate School of Dentistry, Tohoku University, 4-1 Seiryo-machi, Aoba-ku, Sendai 980-8575 (Japan); Kwon, Yong Hoon [Department of Dental Materials, College of Dentistry, Pusan National University, 1-10 Ami-dong, Seo-gu, Pusan 602-739 (Korea, Republic of); Kim, Hyung-Il [Department of Dental Materials, College of Dentistry, Pusan National University, 1-10 Ami-dong, Seo-gu, Pusan 602-739 (Korea, Republic of)]. E-mail: hilkim@pusan.ac.kr

2006-01-05

The age-hardening behaviour, phase transformation and related microstructural changes of an experimental Ag-Cu-Pd-Au alloy were examined by means of hardness test, X-ray diffraction (XRD), scanning electron microscopic (SEM) observations and electron probe microanalysis (EPMA). The specimen alloy showed apparent age-hardenability at the aging temperatures of 350 deg. C and 400 deg. C. By aging the solution-treated specimen at 400 deg. C, two phases of the Ag-rich {alpha}{sub 1} phase and the Pd-containing Cu-rich {alpha}{sub 2} phase were transformed into four phases of the Ag-rich {alpha}{sub 1}{sup '} phase, the Cu-rich {alpha}{sub 2}{sup '} phase, the CsCl-type CuPd phase and the AuCu(I) ordered phase. Microstructure of the solution-treated specimen consisted of the Ag-rich {alpha}{sub 1} matrix, Cu-rich {alpha}{sub 2} particle-like structures of various sizes and the lamellar structure of the {alpha}{sub 1} and {alpha}{sub 2} phases. When the peak hardness was obtained, the very fine lamellar structure consisting of the Ag-rich {alpha}{sub 1}{sup '} and Cu-rich {alpha}{sub 2}{sup '} phases was newly formed in the matrix. By further aging, the very fine lamellar structure grew and coarsened apparently, and the matrix was covered with the coarsened lamellar structure. The hardness increase was considered to be caused mainly by the diffusion and precipitation of Cu from the Ag-rich {alpha}{sub 1} matrix, and the hardness decrease in the latter stage of age-hardening process was caused by the coarsening of the very fine lamellar structure. The CsCl-type CuPd phase and the AuCu(I) ordered phase did not contribute to the hardness increase.

Novel multifunctional graphene sheets with encased Au/Ag nanoparticles for advanced electrochemical analysis of organic compounds.

Science.gov (United States)

Pruneanu, Stela; Biris, Alexandru R; Pogacean, Florina; Lazar, Diana Mihaela; Ardelean, Stefania; Watanabe, Fumyia; Dervishi, Enkeleda; Biris, Alexandru S

2012-11-12

This work is the first presentation of the synthesis of few-layer graphene decorated with gold and silver nanoparticles (Gr-Au-Ag) by chemical vapor deposition over a catalytic system formed of bimetallic Au-Ag nanoclusters supported on MgO and with methane used as the source of carbon. The sheetlike morphology of the graphene nanostructures, with mean sizes in the range of hundreds of nanometers, was observed by high-resolution electron microscopy. The distinctive feature found in all the samples was the regular rectangular or square shapes. This multi-component organic-inorganic nanomaterial was used to modify a platinum substrate and subsequently employed for the detection of carbamazepine, an anti-convulsion drug. UV/Vis spectroscopy revealed that a strong hypochromism occurred over time, after mixing solutions of graphene-Au-Ag with carbamazepine. This can be attributed to π-π stacking between the aromatic groups of the two compounds. Linear sweep voltammetry (LCV) provided evidence that the modified platinum substrate presented a significant electrocatalytic reaction toward the oxidation of carbamazepine. The intensity of the current was found to increase by up to 2.5 times, and the oxidation potential shifted from +1.5 to +1.35 V(Ag/AgCl) in comparison with the unmodified electrode. Electrochemical impedance spectroscopy (EIS) was further used to thoroughly assess the activity of the platinum electrode that was modified by the deposition of the Gr-Au-Ag composites in the presence of various concentrations of carbamazepine. The experimental EIS records were used for the generation of an equivalent electrical circuit, based on the charge-transfer resistance (R(ct)), Warburg impedance (Z(D)), solution resistance (R(s)), and a constant phase element (CPE) that characterizes the non-ideal interface capacitive responses. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Preparation of Agcore/Aushell bimetallic nanoparticles from physical mixtures of Au clusters and Ag ions under dark conditions and their catalytic activity for aerobic glucose oxidation

International Nuclear Information System (INIS)

Zhang, Haijun; Toshima, Naoki; Takasaki, Kanako; Okumura, Mitsutaka

2014-01-01

Graphical abstract: The synthesis, characterization and catalytic activities for glucose oxidation of AgAu bimetallic nanoparticles (BNPs) with size of less than 2 nm are reported. The catalytic activity of Ag 10 Au 90 BNPs was about two times higher than that of Au NPs, even the BNPs have a larger particle size than that of Au NPs. -- Highlights: • Ag core /Au shell BNPs with size of less than 2.0 nm were prepared. • No any reducing reagents and lights were used for the preparation of the BNPs. • The catalytic activity of the BNPs is about two times higher than that of Au NPs. -- Abstract: AgAu bimetallic nanoparticles (BNPs), one of the most extensively studied bimetallic systems in the literatures, could have various structures and compositions depending on their preparation conditions. In the present work, catalytically highly active PVP-protected Ag core /Au shell BNPs of about 2.5 nm in diameter were fabricated from physical mixtures of aqueous dispersions of Au nanoparticles and Ag + ions under dark conditions without using any reducing agents. The prepared Ag core /Au shell BNP colloidal catalysts, which possessed a high activity for aerobic glucose oxidation, were characterized by Ultraviolet–visible spectrophotometry (UV–Vis), Inductive coupled plasma emission spectrometer (ICP), Transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and Energy disperse spectroscopy (EDS) in High-resolution scanning transmission electron microscopy (HR-STEM). The highest activity (11,360 mol-glucose h −1 mol-metal −1 ) was observed for the BNPs with the Ag/Au atomic ratio of 1/9, the TOF value of which is about two times higher than that of Au nanoparticles with the particle size of 1.3 nm. The enhanced catalytic activity of the prepared Ag core /Au shell BNPs compared to Au NPs can be ascribed to the presence of negatively charged Au atoms resulted from electron donations from neighboring Ag atoms and PVP due to electronic charge

Epithermal neutron activation analysis of blue-green algae Spirulina Platensis as a matrix for selenium-containing pharmaceuticals

International Nuclear Information System (INIS)

Mosulishvili, L.M.; Kirkesali, E.I.; Belokobyl'skij, A.I.; Khizanishvili, A.I.; Frontas'eva, M.V.; Gundorina, S.F.; Oprea, C.D.

2000-01-01

To evaluate the potentiality of the blue-green algae Spirulina Platensis as a matrix for the production of Se-containing pharmaceuticals, the background levels of 31 major, minor and trace elements (Na, Mg, Al, Cl, K, Ca, Sc, V, Cr, Mn, Fe, Co, Ni (using (n,p)-reaction), As, Br, Zn, Rb, Mo, Ag, Sb, I, Ba, Sm, Tb, Tm, Hf, Ta, W, Au, Hg, Th) in Spirulina Platensis biomass were determined by means of epithermal neutron activation analysis. The possibility of the purpose-oriented incorporation of Se into Spirulina Platensis biomass was demonstrated. The polynomial dependence of the Se accumulation on nutritional medium loading was revealed. The employed analytical technique allows one to reliably control the amount of toxic elements in algae Spirulina Platensis. Based on this study, a conclusion of the possibility to use Spirulina Platensis as a matrix for the production of Se-containing pharmaceuticals was drawn

Carbon dot-Au(i)Ag(0) assembly for the construction of an artificial light harvesting system.

Science.gov (United States)

Jana, Jayasmita; Aditya, Teresa; Pal, Tarasankar

2018-03-06

Artificial light harvesting systems (LHS) with inorganic counterparts are considered to be robust as well as mechanistically simple, where the system follows the donor-acceptor principle with an unchanged structural pattern. Plasmonic gold or silver nanoparticles are mostly chosen as inorganic counterparts to design artificial LHS. To capitalize on its electron accepting capability, Au(i) has been considered in this work for the synergistic stabilization of a system with intriguingly fluorescing silver(0) clusters produced in situ. Thus a stable fluorescent Au(i)Ag(0) assembly is generated with electron accepting capabilities. On the other hand, carbon dots have evolved as new fluorescent probes due to their unique physicochemical properties. Utilizing the simple electronic behavior of carbon dots, an electronic interaction between the fluorescent Au(i)Ag(0) and a carbon dot has been investigated for the construction of a new artificial light harvesting system. This coinage metal assembly allows surface energy transfer where it acts as an acceptor, while the carbon dot behaves as a good donor. The energy transfer efficiency has been calculated experimentally to be significant (81.3%) and the Au(i)Ag(0)-carbon dot assembly paves the way for efficient artificial LHS.

A novel surface plasmon resonance biosensor based on the PDA-AgNPs-PDA-Au film sensing platform for horse IgG detection

Science.gov (United States)

Wang, Ning; Zhang, Di; Deng, Xinyu; Sun, Ying; Wang, Xinghua; Ma, Pinyi; Song, Daqian

2018-02-01

Herein we report a novel polydopamine-silver nanoparticle-polydopamine-gold (PDA-AgNPs-PDA-Au) film based surface plasmon resonance (SPR) biosensor for horse IgG detection. The PDA-AgNPs-PDA-Au film sensing platform was built on Au-film via layer-by-layer self-assembly. Ag ion was reduced in situ to AgNPs in presence of PDA. The top PDA layer can prevent AgNPs from being oxidized and connect with antibody via Schiff alkali reaction directly. The morphology and thickness of the modified gold film were characterized using scanning electron microscope and Talystep. Experimental results show that the PDA-AgNPs-PDA-Au film sensing platform is stable, regenerative and sensitive for horse IgG detection. The detection limit of horse IgG obtained with the present biosensor is 0.625 μg mL- 1, which is 2-fold and 4-fold lower than that obtained with biosensor based on PDA modified Au film and conventional biosensor based on MPA, respectively. Furthermore, when challenged to real serum samples, our sensor exhibited excellent specificity to horse IgG, suggesting its potential for industrial application.

Strong enhancement of the electrochemiluminescence of luminol by AuAg and PtAg alloy nanoclusters, and its sensitization by phenolic artificial oestrogens

International Nuclear Information System (INIS)

Wang, Ke; Tu, Yifeng; Wei, Xiuhua

2014-01-01

This paper reports on the synthesis of AuAg and PtAg alloy nanoclusters (NCs) and their enhancement effect on the electrochemiluminescence (ECL) of luminol. The conditions of synthesis were optimized, and the structure and properties of the NCs were characterized by X-ray diffraction, transmission electron microscopy, electrochemistry, and optical spectroscopy. The NCs are found to intensify (by up to 20 times) the ECL of luminol in solution of pH 8.5. This finding can largely extend the useful pH range of the ECL of luminol. The enhanced ECL is strongly affected by oxygen and hydrogen peroxide, and the mechanism of enhancement is attributed to the accelerated production of reactive oxygen species. The enhanced ECL is also affected by phenolic artificial estrogens, and this was used for their determination with detection limits as low as 700 pg L −1 (with AuAg) and 1.6 ng L −1 (with PtAg). The method was applied to the determination of such estrogens in egg samples using diethylstilbestrol as a reference substance. (author)

Leaching of Au, Ag, and Pd from waste printed circuit boards of mobile phone by iodide lixiviant after supercritical water pre-treatment.

Science.gov (United States)

Xiu, Fu-Rong; Qi, Yingying; Zhang, Fu-Shen

2015-07-01

Precious metals are the most attractive resources in waste printed circuit boards (PCBs) of mobile phones. In this work, an alternative process for recovering Au, Ag, and Pd from waste PCBs of mobile phones by supercritical water oxidation (SCWO) pre-treatment combined with iodine-iodide leaching process was developed. In the process, the waste PCBs of mobile phones were pre-treated in supercritical water, then a diluted hydrochloric acid leaching (HL) process was used to recovery the Cu, whose leaching efficiency was approximately 100%, finally the resulting residue was subjected to the iodine-iodide leaching process for recovering the Au, Ag, and Pd. Experimental results indicated that SCWO pre-treatment temperature, time, and pressure had significant influence on the Au, Ag, and Pd leaching from (SCWO+HL)-treated waste PCBs. The optimal SCWO pre-treatment conditions were 420°C and 60min for Au and Pd, and 410°C and 30min for Ag. The optimum dissolution parameters for Au, Pd, and Ag in (SCWO+HL)-treated PCBs with iodine-iodide system were leaching time of 120min (90min for Ag), iodine/iodide mole ratio of 1:5 (1:6 for Ag), solid-to-liquid ratio (S/L) of 1:10g/mL (1:8g/mL for Ag), and pH of 9, respectively. It is believed that the process developed in this study is environment friendly for the recovery of Au, Ag, and Pd from waste PCBs of mobile phones by SCWO pre-treatment combined with iodine-iodide leaching process. Copyright © 2015 Elsevier Ltd. All rights reserved.

Probing Interactions between AuNPs/AgNPs and Giant Unilamellar Vesicles (GUVs Using Hyperspectral Dark-field Microscopy

Directory of Open Access Journals (Sweden)

Anupama Bhat

2018-03-01

Full Text Available Noble metallic nanoparticles (NPs such as gold and silver nanoparticles (AuNPs and AgNPs have been shown to exhibit anti-tumor effect in anti-angiogenesis, photothermal and radio therapeutics. On the other hand, cell membranes are critical locales for specific targeting of cancerous cells. Therefore, NP-membrane interactions need be studied at molecular level to help better understand the underlying physicochemical mechanisms for future applications in cancer nanotechnology. Herein, we report our study on the interactions between citrate stabilized colloidal AuNPs/AgNPs (10 nm in size and giant unilamellar vesicles (GUVs using hyperspectral dark-field microscopy. GUVs are large model vesicle systems well established for the study of membrane dynamics. GUVs used in this study were prepared with dimyristoyl phosphatidylcholine (DMPC and doped with cholesterol at various molar concentrations. Both imaging and spectral results support that AuNPs and AgNPs interact very differently with GUVs, i.e., AuNPs tend to integrate in between the lipid bilayer and form a uniform golden-brown crust on vesicles, whereas AgNPs are bejeweled on the vesicle surface as isolated particles or clusters with much varied configurations. The more disruptive capability of AuNPs is hypothesized to be responsible for the formation of golden brown crusts in AuNP-GUV interaction. GUVs of 20 mol% CHOL:DMPC were found to be a most economical concentration for GUVs to achieve the best integrity and the least permeability, consistent with the finding from other phase studies of lipid mixture that the liquid-ordered domains have the largest area fraction of the entire membrane at around 20 mol% of cholesterol.

Conduction and reversible memory phenomena in Au-nanoparticles-incorporated TeO{sub 2}–ZnO films

Energy Technology Data Exchange (ETDEWEB)

Bontempo, L., E-mail: bontempo@usp.br [Laboratório de Sistemas Integráveis, Escola Politécnica da Universidade de São Paulo, Av. Prof. Luciano Gualberto, 158, Travessa 3, 05508-900 São Paulo, SP (Brazil); Laboratório de Materiais Fotônicos e Optoeletrônicos, Faculdade de Tecnologia de São Paulo, Praça Cel. Fernando Prestes, 30, 01124-060 São Paulo, SP (Brazil); Santos Filho, S.G. dos, E-mail: sgsantos@usp.br [Laboratório de Sistemas Integráveis, Escola Politécnica da Universidade de São Paulo, Av. Prof. Luciano Gualberto, 158, Travessa 3, 05508-900 São Paulo, SP (Brazil); Kassab, L.R.P., E-mail: kassablm@osite.com.br [Laboratório de Materiais Fotônicos e Optoeletrônicos, Faculdade de Tecnologia de São Paulo, Praça Cel. Fernando Prestes, 30, 01124-060 São Paulo, SP (Brazil)

2016-07-29

A reversible memory behavior in TeO{sub 2}–ZnO thin films containing Au nanoparticles prepared using the sputtering technique has been observed. The current–voltage characteristics of the films, having Al and Si as electrodes, showed a switching behavior starting from an initial state of low conductivity to a high conductivity one. As a result, an abrupt increase of current (10{sup −7} to 10{sup −3} A) was observed for 6.5 V (100 nm thickness). Au nanoparticles provide a larger electron storage capability, and do not favor the transport through the insulator; they present a higher trapped charge concentration, which reduces the leakage current to lower levels. The influence of the Au nanoparticle diameter and volumetric concentration to reach the abrupt current transition and the value of the transition voltage was studied. These parameters were found to play an important role on reversible memory phenomena as they determine the facility/difficulty to fill and saturate the traps (Au nanoparticles) with electrons. - Highlights: • TeO{sub 2}–ZnO thin films with Au nanoparticles grown by magnetron co-sputtering for memory devices • Nucleation of gold nanoparticles by annealing process • Electrical properties of TeO{sub 2}–ZnO thin films with and without gold nanoparticles • Reversible memory phenomenum in Au-nanoparticles-incorporated TeO{sub 2}–ZnO thin films.

Highly sensitive colorimetric detection of glucose in a serum based on DNA-embeded Au@Ag core–shell nanoparticles

International Nuclear Information System (INIS)

Kang, Fei; Xu, Kun; Hou, Xiangshu

2015-01-01

Glucose is a key energy substance in diverse biology and closely related to the life activities of the organism. To develop a simple and sensitive method for glucose detection is extremely urgent but still remains a key challenge. Herein, we report a colorimetric glucose sensor in a homogeneous system based on DNA-embedded core–shell Au@Ag nanoparticles. In this assay, a glucose substrate was first catalytically oxidized by glucose oxidase to produce H 2 O 2 which would further oxidize and gradually etch the outer silver shell of Au@Ag nanoparticles. Afterwards, the solution color changed from yellow to red and the surface plasmon resonance (SPR) band of Au@Ag nanoparticles declined and red-shifted from 430 to 516 nm. Compared with previous silver-based glucose colorimetric detection strategies, the distinctive SPR band change is superior to the color variation, which is critical to the high sensitivity of this assay. Benefiting from the outstanding optical property, robust stability and well-dispersion of the core–shell Au@AgNPs hybrid, this colorimetric assay obtained a detection limit of glucose as low as 10 nM, which is at least a 10-fold improvement over other AgNPs-based procedures. Moreover, this optical biosensor was successfully employed to the determination of glucose in fetal bovine serum. (paper)

Synthesis of Small Au-Ag Core-Shell Cubes, Cuboctahedra, and Octahedra with Size Tunability and Their Optical and Photothermal Properties.

Science.gov (United States)

Chiang, Chieh; Huang, Michael H

2015-12-02

Aqueous phase synthesis of small Au-Ag core-shell nanocubes, cuboctahedra, and octahedra is achieved through the deposition of Ag shells on small octahedral Au cores. These nanocrystals show efficient photothermal activity and can assemble into supercrystals. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

The Genesis of Precious and Base Metal Mineralization at the Miguel Auza Deposit, Zacatecas, Mexico

Science.gov (United States)

Findley, A. A.; Olivo, G. R.; Godin, L.

2009-05-01

The Miguel Auza mine located in Zacatecas State, Mexico, is a vein-type polymetallic epithermal deposit hosted in deformed argillite, siltstone and, greywacke of the Cretaceous Caracol Formation. Silver-rich base metal veins (0.2 m to >1.5 m wide) are spatially associated with the NE-striking, steeply SE- dipping (70-80°) Miguel Auza fault over a strike length of 1.6 km and a depth of 460 m. A 2 km2 monzonitic stock located in the proximity of the mineralized zones, has previously been interpreted as the source of the mineralizing fluids. Four distinct structural stages are correlated with hydrothermal mineral deposition: (I) The Pre-ore stage is characterized by normal faulting, fracturing of host rock, and rotation of bedding planes. This stage consists of quartz, illite, chlorite, +/- pyrite alteration of sedimentary wall rocks. (II) The Pyrite-vein stage is associated with reverse-sense reactivation of early normal faults, dilation of bedding planes/fractures, and deposition of generally barren calcite + pyrite veinlets. (III) The Main-ore stage is related to the development of reverse-fault- hosted massive sulphide veins. During this stage three phases of mineral deposition are recorded: early pyrite and arsenopyrite, intermediate chalcopyrite, pyrite, arsenopyrite, and base metals, and late base metals and Ag-bearing minerals. Associated gangue minerals during the main ore stage are quartz, muscovite, calcite and chlorite. (IV) The Post-ore stage involves late NW-SE striking block faulting, brecciation and calcite veining. Later supergene oxidation of veins led to deposition of Fe-oxides and hydroxides, commonly filling fractures or replacing early-formed sulphide assemblages. The various vein types display classic epithermal textures including open space filling, banding, comb quartz and brecciation. The Ag-bearing minerals comprise pyrargyrite [Ag3(Sb,As)S3], argentotennantite [(Cu,Ag)10(Zn,Fe)2(Sn,As)4S13], polybasite-pearceite [(Ag,Cu)16(Sb,As)2S11], and

Evaluation of the photophysicochemical properties and photodynamic therapy activity of nanoconjugates of zinc phthalocyanine linked to glutathione capped Au and Au3Ag1 nanoparticles

CSIR Research Space (South Africa)

Oluwole, DA

2018-03-01

Full Text Available , Charles Maphanga, Saturnin Ombinda-Lemboumba, Patience Mthunzi-Kufa, Tebello Nyokong ABSTRACT: We report on the synthesis of glutathione capped gold (AuNPs–GSH) and gold– silver (Au3Ag1NPs–GSH) nanoparticles and their covalent attachment to Zn...

Determination of the compositions of the DIGM zone in nanocrystalline Ag/Au and Ag/Pd thin films by secondary neutral mass spectrometry

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Gábor Y. Molnár

2016-03-01

Full Text Available Alloying by grain boundary diffusion-induced grain boundary migration is investigated by secondary neutral mass spectrometry depth profiling in Ag/Au and Ag/Pd nanocrystalline thin film systems. It is shown that the compositions in zones left behind the moving boundaries can be determined by this technique if the process takes place at low temperatures where solely the grain boundary transport is the contributing mechanism and the gain size is less than the half of the grain boundary migration distance. The results in Ag/Au system are in good accordance with the predictions given by the step mechanism of grain boundary migration, i.e., the saturation compositions are higher in the slower component (i.e., in Au or Pd. It is shown that the homogenization process stops after reaching the saturation values and further intermixing can take place only if fresh samples with initial compositions, according to the saturation values, are produced and heat treated at the same temperature. The reversal of the film sequence resulted in the reversal of the inequality of the compositions in the alloyed zones, which is in contrast to the above theoretical model, and explained by possible effects of the stress gradients developed by the diffusion processes itself.

Fast and facile preparation of CTAB based gels and their applications in Au and Ag nanoparticles synthesis

Energy Technology Data Exchange (ETDEWEB)

Upadhyay, Ravi Kant, E-mail: rkupadhyay85@gmail.com [Department of Chemistry, School of Natural Sciences, Shiv Nadar University, Gautam Budh Nagar, 201314 Uttar Pradesh (India); Soin, Navneet, E-mail: n.soin@bolton.ac.uk [Knowledge Centre for Materials Chemistry (KCMC), Institute for Materials Research and Innovation (IMRI), University of Bolton, Deane Road, Bolton BL3 5AB (United Kingdom); Saha, Susmita, E-mail: ssaha@bose.res.in [Department of Condensed Matter Physics and Material Sciences, S. N. Bose National Centre for Basic Sciences, Block JD, Sector III, Salt Lake, Kolkata 700 098 (India); Barman, Anjan, E-mail: abarman@bose.res.in [Department of Condensed Matter Physics and Material Sciences, S. N. Bose National Centre for Basic Sciences, Block JD, Sector III, Salt Lake, Kolkata 700 098 (India); Sinha Roy, Susanta, E-mail: susanta.roy@snu.edu.in [Department of Physics, School of Natural Sciences, Shiv Nadar University, Gautam Budh Nagar, 201314 Uttar Pradesh (India)

2015-04-15

We have demonstrated that the gel-like mesophase of Cetyltrimethylammonium bromide (CTAB) can be synthesized by judicial adjustment of water to surfactant molar ratio (W{sub 0}), without using any additional salts, gelating agents or co-surfactants. Gel formation was found to be highly dependent on the water to surfactant molar ratio (W{sub 0}), with the lowest value of W{sub 0} (41.5) resulting in rapid gel formation. Environmental scanning electron microscope (ESEM) analysis revealed that the gel was comprised of interconnected cylindrical structures. The presence of hydrogen bonding in the gel-like mesophase was confirmed by Fourier Transform Infrared spectroscopy (FTIR) analysis. Rheology measurements revealed that all the gel samples were highly viscoelastic in nature. Furthermore, Au and Ag containing CTAB gels were explored as precursors for the preparation of spherical Gold (Au) and Silver (Ag) nanoparticles using Sodium borohydride (NaBH{sub 4}) as reducing agent. The effects of NaBH{sub 4} concentration on the particle size and morphology of the Au and Ag nanoparticles have also been studied. - Highlights: • A facile synthesis of CTAB based gel-like mesophase is reported. • CTAB gels were obtained by adjusting water to surfactant molar ratio (W{sub 0}). • FTIR analysis revealed that hydrogen bonding plays a key role in gel formation. • Au, Ag nanoparticles were synthesized by using CTAB gel and NaBH{sub 4}.

CsAg{sub 5}Te{sub 3}: a new metal-rich telluride with a unique tunnel structure

Energy Technology Data Exchange (ETDEWEB)

Jing, Li [Rutgers Univ., Camden, NJ (United States). Dept. of Chem.; Hongyou, Guo [Rutgers Univ., Camden, NJ (United States). Dept. of Chem.; Xiang, Zhang [Michigan State Univ., East Lansing, MI (United States). Dept. of Chemistry; Kanatzidis, M G [Michigan State Univ., East Lansing, MI (United States). Dept. of Chemistry

1995-02-15

The synthesis and structure of a new ternary silver telluride, CsAg{sub 5}Te{sub 3}, is described. The compound was prepared from a Cs{sub 2}Te-CaTe-Te flux but it can also be prepared from a direct combination of Cs{sub 2}Te and Ag{sub 2}Te under vacuum at 600 C. The crystal data for CsAg{sub 5}Te{sub 3} at 20 C (Mo K{alpha} radiation) are as follows: a=14.672(2) A and c=4.601(3) A; V=990.5(8) A{sup 3}; Z=4; D{sub calc}=7.075 g cm{sup -3}; space group, P4{sub 2} /mnm (No. 136); 2{theta}{sub max}=50 ; number of independent data collected, 572; number of data observed with I>3{sigma}(I), 267; number of variables, 32; {mu}=218.51 cm{sup -1}; extinction coefficient, 0.585x10{sup -7}; final R=0.040; R{sub w}=0.046; goodness of fit, 1.42. The compound features a new structure type with Cs{sup +}-filled, relatively large tunnels running through the lattice. The material is a semiconductor with a band gap of about 0.65 eV. ((orig.))

Thermoelectric properties of p-type pseudo-binary (Ag0.365Sb0.558Te) x -(Bi0.5Sb1.5Te3)1-x (x=0-1.0) alloys prepared by spark plasma sintering

International Nuclear Information System (INIS)

Cui, J.L.; Xue, H.F.; Xiu, W.J.; Jiang, L.; Ying, P.Z.

2006-01-01

In this paper, pseudo-binary (Ag 0.365 Sb 0.558 Te) x -(Bi 0.5 Sb 1.5 Te 3 ) 1- x (x=0-1.0) alloys were prepared using spark plasma sintering technique, and the composition-dependent thermoelectric properties were evaluated. Electrical conductivities range from 7.9x10 4 to 15.6x10 4 Ω -1 m -1 at temperatures of 507 and 318 K, respectively, being about 3.0 and 8.5 times those of Bi 0.5 Sb 1.5 Te 3 alloy at the corresponding temperatures. The optimal dimensionless figure of merit (ZT) of the sample with molar fraction x=0.025 reaches 1.1 at 478 K, whereas that of the ternary Bi 0.5 Sb 1.5 Te 3 alloy is 0.58 near room temperature. The results also reveal that a direct introduction of Ag 0.365 Sb 0.558 Te in the Bi-Sb-Te system is much more effective to the property improvement than naturally precipitated Ag 0.365 Sb 0.558 Te in the Ag-doped Ag-Bi-Sb-Te system. - Graphical abstract: The temperature dependence of the dimensionless thermoelectric figure of merit ZT for different (Ag 0.365 Sb 0.558 Te) x -(Bi 0.5 Sb 1.5 Te 3 ) 1- x (x=0-1.0) alloys prepared by spark plasma sintering

Comment on ``(Au-Ag)144(SR)60 alloy nanomolecules'' by C. Kumara and A. Dass, Nanoscale, 2011, 3, 3064

Science.gov (United States)

Barcaro, Giovanni; Sementa, Luca; Fortunelli, Alessandro; Stener, Mauro

2015-04-01

A recent paper in this journal reported the synthesis and characterization via electrospray ionization mass spectroscopy and UV-vis spectroscopy of (Au-Ag)144(SR)60 alloy nanomolecules with different compositions, ranging from 1 : 0 to 1 : 0.75 Au : Ag ratios. The UV-vis spectra of such systems were found to exhibit absorption peaks at 310 nm, 425 nm and 560 nm, interpreted as reminiscent of the silver surface plasmon resonance band due to simple atomic replacement of Au by Ag atoms in a fixed structural framework. On the basis of a comparison of experimentally observed and theoretically simulated optical absorption spectra, we conclude that the experimental situation must be more complicated, and that further work is needed to achieve atomistic insight into these fascinating systems.

Nanoscale nuclei in phase change materials: Origin of different crystallization mechanisms of Ge2Sb2Te5 and AgInSbTe

International Nuclear Information System (INIS)

Lee, Bong-Sub; Bogle, Stephanie N.; Darmawikarta, Kristof; Abelson, John R.; Shelby, Robert M.; Retter, Charles T.; Burr, Geoffrey W.; Raoux, Simone; Bishop, Stephen G.

2014-01-01

Phase change memory devices are based on the rapid and reversible amorphous-to-crystalline transformations of phase change materials, such as Ge 2 Sb 2 Te 5 and AgInSbTe. Since the maximum switching speed of these devices is typically limited by crystallization speed, understanding the crystallization process is of crucial importance. While Ge 2 Sb 2 Te 5 and AgInSbTe show very different crystallization mechanisms from their melt-quenched states, the nanostructural origin of this difference has not been clearly demonstrated. Here, we show that an amorphous state includes different sizes and number of nanoscale nuclei, after thermal treatment such as melt-quenching or furnace annealing is performed. We employ fluctuation transmission electron microscopy to detect nanoscale nuclei embedded in amorphous materials, and use a pump-probe laser technique and atomic force microscopy to study the kinetics of nucleation and growth. We confirm that melt-quenched amorphous Ge 2 Sb 2 Te 5 includes considerably larger and more quenched-in nuclei than its as-deposited state, while melt-quenched AgInSbTe does not, and explain this contrast by the different ratio between quenching time and nucleation time in these materials. In addition to providing insights to the crystallization process in these technologically important devices, this study presents experimental illustrations of temperature-dependence of nucleation rate and growth speed, which was predicted by theory of phase transformation but rarely demonstrated

The photovoltaic performance of Ag2S quantum dots-sensitized solar cells using plasmonic Au nanoparticles/TiO2 working electrodes

Science.gov (United States)

Badawi, Ali; Mostafa, Nasser Y.; Al-Hosiny, Najm M.; Merazga, Amar; Albaradi, Ateyyah M.; Abdel-Wahab, F.; Atta, A. A.

2018-06-01

The photovoltaic performance of silver sulfide (Ag2S) quantum dots-sensitized solar cells (QDSSCs) using different concentrations (0, 0.05, 0.1, 0.3 and 0.5 wt.%) of plasmonic Au nanoparticles (NPs)/titania (TiO2) electrodes has been investigated. Ag2S quantum dots (QDs) were adsorbed onto the Au NPs/titania electrodes using the successive ionic layer adsorption and reaction (SILAR) deposition technique. The morphological properties of the Au NPs and the prepared titania electrodes were characterized using transmission electron microscope (TEM) and scanning electron microscope (SEM), respectively. The energy-dispersive X-ray (EDX) spectra of the bare titania and Ag2S QDs-sensitized titania electrodes were recorded. The optical properties of the prepared Ag2S QDs-sensitized titania electrodes were measured using a UV-visible spectrophotometer. The estimated energy band gap of Ag2S QDs-sensitized titania electrodes is 1.96 eV. The photovoltaic performance of the assembled Ag2S QDSSCs was measured under 100 mW/cm2 solar illumination. The optimal photovoltaic parameters were obtained as follows: open circuit voltage Voc = 0.50 V, current density Jsc = 3.18 mA/cm2, fill factor (FF) = 0.35 and energy conversion efficiency η = 0.55% for 0.3 wt.% of Au NPs/titania electrode. These results are attributed to the enhancement in the absorption and decrease in the electron-hole pairs recombination rate. The open circuit voltage decay (OCVD) measurements of the assembled Ag2S QDSSCs were measured. The calculated electron lifetime (τ) in Ag2S QDSSCs with Au NPs/titania electrodes is at least one order of magnitude more than that with bare titania electrode. The cut-on-cut-off cycles of the solar illumination measurements show the rapid sensitivity and good reproducibility of the assembled Ag2S QDSSCs.

Label-free sensitive luminescence biosensor for immunoglobulin G based on Ag6Au6 ethisterone cluster-estrogen receptor α aggregation and graphene.

Science.gov (United States)

Chen, Nannan; Guo, Wenjing; Lin, Zhixiang; Wei, Qiaohua; Chen, Guonan

2018-08-01

A specific and label-free "on-off-on" luminescence biosensor based on a novel heterometallic cluster [Ag 6 Au 6 (ethisterone) 12 ]-estrogen receptor α (Ag 6 Au 6 Eth-ERα) aggregation utilizing graphene oxide (GO) as a quencher to lead a small background signal was firstly constructed to detect immunoglobulin G (IgG) with a simple process and high selectivity. The efficient photoluminescent (PL) Ag 6 Au 6 Eth-ERα aggregation is strongly quenched by GO. In the presence of IgG, the PL of this system will be restored, and perceivable by human eyes under UV lamp excitation (365 nm). The quenching mechanism of GO on Ag 6 Au 6 Eth-ERα and enhancement mechanism of IgG on Ag 6 Au 6 Eth-ERα-GO were investigated in detail. Under the optimum conditions, the biosensor for high sensitive IgG detection expressed a wider linear range of 0.0078-10 ng/mL and a lower detection limit of 0.65 pg/mL with good stability and repeatability, which provided a new approach for label-free IgG detection. Copyright © 2018 Elsevier B.V. All rights reserved.

Highly efficient and porous TiO{sub 2}-coated Ag@Fe{sub 3}O{sub 4}@C-Au microspheres for degradation of organic pollutants

Energy Technology Data Exchange (ETDEWEB)

Shen, Mao, E-mail: shenmao19820808@163.com; Chen, Suqing, E-mail: 465060605@qq.com; Jia, Wenping, E-mail: tzcjwp@tzc.edu.cn [Taizhou University, College of Pharmaceutical and Chemical Engineering (China); Fan, Guodong, E-mail: fangd@sust.edu.cn [Shan xi University of Science and Technology, Key Laboratory of Auxiliary Chemistry and Technology for Chemical Industry, Ministry of Education (China); Jin, Yanxian, E-mail: shirleyj@tzc.edu.cn; Liang, Huading, E-mail: shanjian8208@163.com [Taizhou University, College of Pharmaceutical and Chemical Engineering (China)

2016-12-15

In this paper, we reported a novel hierarchical porous Ag@Fe{sub 3}O{sub 4}@C-Au@TiO{sub 2} core@shell microspheres with a highly photocatalytic activity and magnetically separable properties. The synthesis method is included of a Fe{sub 3}O{sub 4} magnetic embedded Ag core (Ag@Fe{sub 3}O{sub 4}), an interlayer of carbon modified by PEI to form sufficient amounts of amine functional groups (Ag@Fe{sub 3}O{sub 4}@C-PEI), the grafting of Au nanoparticles on the surface of Ag@Fe{sub 3}O{sub 4}@C-PEI (Ag@Fe{sub 3}O{sub 4}@C-Au), and an ordered porous TiO{sub 2} structured shell. As an example of the applications, the photocatalytic activities of the samples were investigated by the reduction of Rhodamine B (RhB) under visible-light irradiation. The results show that the porous Ag@Fe{sub 3}O{sub 4}@C-Au@TiO{sub 2} core@shell microspheres display higher adsorption and photocatalytic activities compared to the pure porous TiO{sub 2} and Ag@Fe{sub 3}O{sub 4}@C@TiO{sub 2} microspheres, which are attributed to the local surface plasmon resonance (LSPR) by the Ag and Au nanoparticles and the high specific surface area.

Molecular dynamics simulation of joining process of Ag-Au nanowires and mechanical properties of the hybrid nanojoint

Directory of Open Access Journals (Sweden)

Su Ding

2015-05-01

Full Text Available The nanojoining process of Ag-Au hybrid nanowires at 800K was comprehensively studied by virtue of molecular dynamics (MD simulation. Three kinds of configurations including end-to-end, T-like and X-like were built in the simulation aiming to understand the nanojoining mechanism. The detailed dynamic evolution of atoms, crystal structure transformation and defects development during the nanojoining processes were performed. The results indicate that there are two stages in the nanojoining process of Ag-Au nanowires which are atom diffusion and new bonds formation. Temperature is a key parameter affecting both stages ascribed to the energy supply and the optimum temperature for Ag-Au nanojoint with diameter of 4.08 nm has been discussed. The mechanical properties of the nanojoint were examined with simulation of tensile test on the end-to-end joint. It was revealed that the nanojoint was strong enough to resist fracture at the joining area.

Growth and morphological analysis of segmented AuAg alloy nanowires created by pulsed electrodeposition in ion-track etched membranes

Directory of Open Access Journals (Sweden)

Ina Schubert

2015-06-01

Full Text Available Background: Multicomponent heterostructure nanowires and nanogaps are of great interest for applications in sensorics. Pulsed electrodeposition in ion-track etched polymer templates is a suitable method to synthesise segmented nanowires with segments consisting of two different types of materials. For a well-controlled synthesis process, detailed analysis of the deposition parameters and the size-distribution of the segmented wires is crucial.Results: The fabrication of electrodeposited AuAg alloy nanowires and segmented Au-rich/Ag-rich/Au-rich nanowires with controlled composition and segment length in ion-track etched polymer templates was developed. Detailed analysis by cyclic voltammetry in ion-track membranes, energy-dispersive X-ray spectroscopy and scanning electron microscopy was performed to determine the dependency between the chosen potential and the segment composition. Additionally, we have dissolved the middle Ag-rich segments in order to create small nanogaps with controlled gap sizes. Annealing of the created structures allows us to influence their morphology.Conclusion: AuAg alloy nanowires, segmented wires and nanogaps with controlled composition and size can be synthesised by electrodeposition in membranes, and are ideal model systems for investigation of surface plasmons.

Fabrication of Au/graphene oxide/Ag sandwich structure thin film and its tunable energetics and tailorable optical properties

OpenAIRE

Ruijin Hong; Jialin Ji; Chunxian Tao; Daohua Zhang; Dawei Zhang

2017-01-01

Au/graphene oxide/Ag sandwich structure thin film was fabricated. The effects of graphene oxide (GO) and bimetal on the structure and optical properties of metal silver films were investigated by X-ray diffraction (XRD), optical absorption, and Raman intensity measurements, respectively. Compared to silver thin film, Au/graphene oxide/Ag sandwich structure composite thin films were observed with wider optical absorption peak and enhanced absorption intensity. The Raman signal for Rhodamine B ...

Fluid Inclusion Study of The Tumpangpitu High Sulfidation Epithermal Gold Deposit in Banyuwangi District, East Java, Indonesia

Directory of Open Access Journals (Sweden)

Yu Yu Myaing

2018-03-01

Full Text Available The Tumpangpitu high sulfidation (HS epithermal gold deposit is located in the south coast of East Java, Banyuwangi District, East Java Province, Indonesia. This area lies within the central portion of the Cenozoic Sunda‐Banda magmatic arc which trends southeast from northern Sumatra to west Java then eastward through east Java, Bali, Lombok, Sumbawa and terminating at Banda sea. The geology of the Tumpangpitu is predominantly occupied by Late Oligocene to Middle Miocene low-K calc-alkaline to alkaline andesitic volcanic rocks and interbedded with volcaniclastic rock sequences, which are associated with low-K intermediate intrusions. The mineralization style at the Tumpangpitu area is composed of a high‐sulfidation (HS epithermal gold-copper system which is typically associated with concealed gold-rich porphyry copper system. The HS epithermal mineralization is hosted by volcanic and volcaniclastic rocks in this research area. The mineralization domains are divided into Zone A, Zone B and Zone C which are situated along NW-SE-trending silica ledges zones. The HS epithermal mineralization is texturally occurs as vuggy replacements mineralization as well as stockworks, disseminated forms, fractures and veins. Fluid inclusion study was conducted for 6 quartz vein samples which petrographically entrapped fluid inclusions. Homogenization temperature (Th and melting temperature (Tm can microthermometrically be determined by fluid inclusion analysis. The average homogenization temperature (Th of the fluid inclusions gives 180˚C to 342˚C and melting temperature are from -0.1 ˚C to -1.4˚C. Tm corresponds to the salinities ranging from 0.1 to 4.5 wt% NaCl equivalent. The paleodepth of ore formation can be estimated from the salinity of fluid. Since the deposit was not formed at boiling condition, the minimum paleodepth of ore (quartz samples taken from both shallow level (53.35 m and deep level (135.15 m is determined at 650m and 1,220 m

Electrodeposition of Au/Ag bimetallic dendrites assisted by Faradaic AC-electroosmosis flow

Energy Technology Data Exchange (ETDEWEB)

Ji, Jianlong; Li, Pengwei; Sang, Shengbo, E-mail: sbsang@tyut.edu.cn; Zhang, Wendong, E-mail: wdzhang@tyut.edu.cn; Li, Gang; Hu, Jie [Micro and Nano-system Research Centre, College of Information Engineering, Taiyuan University of Technology, 030024, Taiyuan (China); Zhou, Zhaoying, E-mail: zhouzy@mail.tsinghua.edu.cn; Yang, Xing; Dong, Hualai [MEMS Laboratory, Department of Precision Instruments, Tsinghua University, 100084, Beijing (China)

2014-03-15

Au/Ag bimetallic dendrites were synthesized successfully from the corresponding aqueous solution via the AC electrodeposition method. Both of the morphologies and compositions could be tuned by the electrolyte concentration and AC frequency. The prepared bimetallic dendrites were characterized by scanning electron microscopy (SEM), energy dispersive X-ray spectrometer (EDS), transmission electron microscopy (TEM) and UV–vis spectroscopy. The underlying dendrite growth mechanism was then proposed in the context of the Directed Electrochemical Nanowires Assembly (DENA) models. Owing to the unscreened voltage dropping in the electrolyte bulk, electromigration dominates the species flux process, and cations tend to accumulate in areas with strong electric field intensity, such as electrode edges. Moreover, Faradaic AC-electro-osmosis (ACEO) flow could increase the effective diffusion layer thickness in these areas during the electrochemical reaction, and leads to dendrite growth. Further Micro-Raman observations illustrated that the Au/Ag bimetallic dendrites exhibited pronounced surface-enhanced Raman scattering (SERS) activity, using 4-mercaptopyridine (4-MP) as model molecules.

Electrodeposition of Au/Ag bimetallic dendrites assisted by Faradaic AC-electroosmosis flow

Directory of Open Access Journals (Sweden)

Jianlong Ji

2014-03-01

Full Text Available Au/Ag bimetallic dendrites were synthesized successfully from the corresponding aqueous solution via the AC electrodeposition method. Both of the morphologies and compositions could be tuned by the electrolyte concentration and AC frequency. The prepared bimetallic dendrites were characterized by scanning electron microscopy (SEM, energy dispersive X-ray spectrometer (EDS, transmission electron microscopy (TEM and UV–vis spectroscopy. The underlying dendrite growth mechanism was then proposed in the context of the Directed Electrochemical Nanowires Assembly (DENA models. Owing to the unscreened voltage dropping in the electrolyte bulk, electromigration dominates the species flux process, and cations tend to accumulate in areas with strong electric field intensity, such as electrode edges. Moreover, Faradaic AC-electro-osmosis (ACEO flow could increase the effective diffusion layer thickness in these areas during the electrochemical reaction, and leads to dendrite growth. Further Micro-Raman observations illustrated that the Au/Ag bimetallic dendrites exhibited pronounced surface-enhanced Raman scattering (SERS activity, using 4-mercaptopyridine (4-MP as model molecules.

Utilization of epithermal neutrons for the determination of molybdenum in the presence of uranium

International Nuclear Information System (INIS)

Oliveira Melo, M.A.M. de.

1984-05-01

Activation analysis by means of selective activation with epithermal neutrons is proposed for the determination of molybdenum in samples when uranium is present. Instrumental activation analysis with epithermal neutrons is advantageous for the determination of elements with large resonance integral, as compared to its thermal neutron activation cross section. The main reason for using this method is the serious interference caused by 99 Mo produced by fission of 235 U. This effect is strongly reduced by using the epicadmium irradiation technique. The filter efficiency has been investigated by irradiation experiments with bare and cadmium-covered samples. A solvent extraction process for uranium, before irradiation, is proposed to reduce sample background. The determination of Mo in leach samples is proposed in order to support the analytical needs of Figueira and Pocos de Caldas Mineral Prospection Programme of Departamento de Tecnologia Mineral from CDTN/NUCLEBRAS (MG,Brazil). The introduction of activation analysis with epithermal neutrons as a routine analytical tool in CDTN is our main goal. This method represents one more opportunity for exploring the analytical facilities available at TRIGA MARK I IPR-R1 nuclear reactor. (Author) [pt

LA-ICP-MS U-Th-Pb Dating and Trace Element Geochemistry of Allanite: Implications on the Different Skarn Metallogenesis between the Giant Beiya Au and Machangqing Cu-Mo-(Au Deposits in Yunnan, SW China

Directory of Open Access Journals (Sweden)

Yu Fu

2017-12-01

Full Text Available The giant Beiya Au skarn deposit and Machangqing porphyry Cu-Mo-(Au deposit are located in the middle part of the Jinshajiang–Ailaoshan alkaline porphyry metallogenic belt. The Beiya deposit is the largest Au skarn deposit in China, whilst the Machangqing deposit comprises a well-developed porphyry-skarn-epithermal Cu-Mo-(Au mineral system. In this paper, we present new allanite U-Th-Pb ages and trace element geochemical data from the two deposits and discuss their respective skarn metallogenesis. Based on the mineral assemblage, texture and Th/U ratio, the allanite from the Beiya and Machangqing deposits are likely hydrothermal rather than magmatic. Laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS allanite U-Th-Pb dating has yielded Th-Pb isochron ages of 33.4 ± 4.6 Ma (MSWD = 0.22 (Beiya and 35.4 ± 9.8 Ma (MSWD = 0.26 (Machangqing, representing the retrograde alteration and magnetite skarn mineralization age of the two deposits. The Beiya and Machangqing alkali porphyry-related mineralization are synchronous and genetically linked to the magmatic hydrothermal activities of the Himalayan orogenic event. Major and trace element compositions reveal that the Beiya allanite has higher Fe3+/(Fe3+ + Fe2+ ratios, U content and Th content than the Machangqing allanite, which indicate a higher oxygen fugacity and F content for the ore-forming fluids at Beiya. Such differences in the ore-forming fluids may have contributed to the different metallogenic scales and metal types in the Beiya and Machangqing deposit.

gold mineralization in Masjeddaghi area, east of Jolfa, NW Iran

OpenAIRE

Ali Imamalipour; Hossein Abdoli; Behzad Hajalilo

2010-01-01

Two types of mineralization including porphyry copper and epithermal gold mineralization have occurred in relation with an intermediate volcano-plutonic complex in Masjeddaghi area. Different alterations including silica, advanced argillic, intermediate argillic and propylitic have been distinguished in relation with epithermal mineralization, which have a zonal pattern. Elemental mass gains and losses during alterations were calculated using Zr as an immobile monitor. Silica zone has enriche...

Sulfonated poly(ether ether ketone)/poly(vinyl alcohol) sensitizing system for solution photogeneration of small Ag, Au, and Cu crystallites.

Science.gov (United States)

Korchev, A S; Shulyak, T S; Slaten, B L; Gale, W F; Mills, G

2005-04-28

Illumination of air-free aqueous solutions containing sulfonated poly(ether ether ketone) and poly(vinyl alcohol) with 350 nm light results in benzophenone ketyl radicals of the polyketone. The polymer radicals form with a quantum yield 0.02 and decay with a second-order rate constant 6 orders of magnitude lower than that of typical alpha-hydroxy radicals. Evidence is presented that the polymeric benzophenone ketyl radicals reduce Ag+, Cu2+, and AuCl4- to metal particles of nanometer dimensions. Decreases in the reduction rates with increasing Ag(I), Cu(II), and Au(III) concentrations are explained using a kinetic model in which the metal ions quench the excited state of the polymeric benzophenone groups, which forms the macromolecular radicals. Quenching is fastest for Ag+, whereas Cu2+ and AuCl4- exhibit similar rate constants. Particle formation becomes more complex as the number of equivalents needed to reduce the metal ions increases; the Au(III) system is an extreme case where the radical reactions operate in parallel with secondary light-initiated and thermal reduction channels. For each metal ion, the polymer-initiated photoreactions produce crystallites possessing distinct properties, such as a very strong plasmon in the Ag case or the narrow size distribution exhibited by Au particles.

Binding Affinity of a Highly Sensitive Au/Ag/Au/Chitosan-Graphene Oxide Sensor Based on Direct Detection of Pb2+ and Hg2+ Ions

Directory of Open Access Journals (Sweden)

Nur Hasiba Kamaruddin

2017-10-01

Full Text Available The study of binding affinity is essential in surface plasmon resonance (SPR sensing because it allows researchers to quantify the affinity between the analyte and immobilised ligands of an SPR sensor. In this study, we demonstrate the derivation of the binding affinity constant, K, for Pb2+ and Hg2+ ions according to their SPR response using a gold/silver/gold/chitosan–graphene oxide (Au/Ag/Au/CS–GO sensor for the concentration range of 0.1–5 ppm. The higher affinity of Pb2+ to binding with the CS–GO sensor explains the outstanding sensitivity of 2.05 °ppm−1 against 1.66 °ppm−1 of Hg2+. The maximum signal-to-noise ratio (SNR upon detection of Pb2+ is 1.53, and exceeds the suggested logical criterion of an SNR. The Au/Ag/Au/CS–GO SPR sensor also exhibits excellent repeatability in Pb2+ due to the strong bond between its functional groups and this cation. The adsorption data of Pb2+ and Hg2+ on the CS–GO sensor fits well with the Langmuir isotherm model where the affinity constant, K, of Pb2+ and Hg2+ ions is computed. The affinity of Pb2+ ions to the Au/Ag/Au/CS–GO sensor is significantly higher than that of Hg2+ based on the value of K, 7 × 105 M−1 and 4 × 105 M−1, respectively. The higher shift in SPR angles due to Pb2+ and Hg2+ compared to Cr3+, Cu2+ and Zn2+ ions also reveals the greater affinity of the CS–GO SPR sensor to them, thus supporting the rationale for obtaining K for these two heavy metals. This study provides a better understanding on the sensing performance of such sensors in detecting heavy metal ions.

Rapidity densities and their fluctuations in central 200 A GeV 32S interactions with Au and Ag, Br nuclei

International Nuclear Information System (INIS)

Adamovich, M.I.; Alexandrov, Y.A.; Chernyavsky, M.M.; Gerassimov, S.G.; Kharlamov, S.P.; Larionova, V.G.; Orlova, G.I.; Peresadko, N.G.; Salmanova, N.A.; Tretyakova, M.I.; Andreeva, N.P.; Anson, Z.V.; Ameeva, Z.V.; Bubnov, V.I.; Chasnicov, I.Y.; Eremenko, L.E.; Eligbaeva, G.Z.; Gaitinov, A.S.; Kalyachkina, G.S.; Kanygina, E.K.; Shakhova, T.I.; Azimov, S.A.; Chernova, L.P.; Gadzhieva, S.I.; Gulamov, K.G.; Kadyrov, F.G.; Lukicheva, N.S.; Navotny, V.S.; Svechnikova, L.N.; Bhasin, A.; Kachroo, S.; Kaul, G.L.; Mangotra, L.K.; Rao, N.K.; Burnett, T.H.; Grote, J.; Koss, T.; Lord, J.; Skelding, D.; Strausz, S.; Wilkes, R.J.; Cai, X.; Liu, L.S.; Maslennikova, N.V.; Qian, W.Y.; Wang, H.Q.; Zhou, D.C.; Zhou, J.C.; Dressel, B.; Ganssauge, E.R.; Hackel, S.; Kallies, H.; Mueller, C.; Rhee, J.T.; Schultz, W.; Garpman, S.; Otterlund, I.; Persson, S.; Soderstrom, K.; Stenlund, E.; Judek, B.; Storey, R.S.; Xu, G.F.; Zheng, P.Y.; Zhang, D.H.

1989-01-01

The pseudo-rapidity density distributions of shower particles (n s ) are measured in central inelastic S+Au and S+Ag, Br interactions. The extracted maximum energy densities, while being higher for Au than for Ag,Br interactions, were found to be similar to those obtained for oxygen emulsion interactions. The correlation between rapidity density and shower particle multiplicity shows a small deviation from the Lund Model Fritiof for the highest energy densities in S+Au interactions, whereas the bulk of the data yields satisfactory agreement. (orig.)

The Kongsberg silver deposits, Norway: Ag-Hg-Sb mineralization and constraints for the formation of the deposits

Science.gov (United States)

Kotková, Jana; Kullerud, Kåre; Šrein, Vladimír; Drábek, Milan; Škoda, Radek

2018-04-01

The Kongsberg silver district has been investigated by microscopy and electron microprobe analysis, focusing primarily on the Ag-Hg-Sb mineralization within the context of the updated mineral paragenesis. The earliest mineralization stage is represented by sulfides, including acanthite, and sulfosalts. Native silver formed initially through breakdown of early Ag-bearing phases and later through influx of additional Ag-bearing fluids and silver remobilization. The first two generations of native silver were separated in time by the formation of Ni-Co-Fe sulfarsenides and the monoarsenide niccolite along rims of silver crystals. The presence of As-free sulfosalts and the absence of di- and tri-arsenides suggest a lower arsenic/sulfur activity ratio for the Kongsberg deposits compared to other five-element deposits. Native silver shows binary Ag-Hg and Ag-Sb solid solutions, in contrast to the ternary Ag-Hg-Sb compositions typical for other deposits of similar type. Antimonial silver together with allargentum, dyscrasite, and pyrargyrite was documented exclusively from the northern area of the district. Elsewhere, the only Sb-bearing minerals are polybasite and tetrahedrite/freibergite. Hg-rich silver (up to 21 wt% Hg) has been documented only in the central-western area. Myrmekite of freibergite and chalcopyrite reflects exsolution from an original Ag-poor tetrahedrite upon cooling, while myrmekite of pyrite and silver, forming through breakdown of low-temperature phases (argentopyrite or lenaite) upon heating, characterizes the Kongsberg silver district. Based on the stabilities of minerals and mineral assemblages, the formation of the silver mineralization can be constrained to temperatures between 180 and 250 °C.

Selective etching characteristics of the AgInSbTe phase-change film in laser thermal lithography

International Nuclear Information System (INIS)

Li, Hao; Geng, Yongyou; Wu, Yiqun

2012-01-01

In the current work, the etching selectivity of the AgInSbTe phase-change film in laser thermal lithography is reported for the first time. Film phase change induced by laser irradiation and etching selectivity to crystalline and amorphous states in different etchants, including hydrochloric acid, sulfuric acid, phosphoric acid, nitric acid, sodium hydroxide, sodium sulfide, ammonium sulfide and ammonium hydroxide, are investigated. The results indicated that ammonium sulfide solvent (2.5 mol/L) had excellent etching selectivity to crystalline and amorphous states of the AgInSbTe film, and the etching characteristics were strongly influenced by the laser power density and laser irradiation time. The etching rate of the crystalline state of the AgInSbTe film was 40.4 nm/min, 20 times higher than that of the amorphous state under optimized irradiation conditions (power density: 6.63 mW/μm 2 and irradiation time: 330 ns), with ammonium sulfide solvent (2.5 mol/L) as etchant. The step profile produced in the selective etching was clear, and smooth surfaces remained both on the step-up and step-down with a roughness of less than 4 nm (10 x 10 μm). The excellent performance of the AgInSbTe phase-change film in selective etching is significant for fabrication of nanostructures with super-resolution in laser thermal lithography. (orig.)

Silica-covered star-shaped Au-Ag nanoparticles as new electromagnetic nanoresonators for Raman characterisation of surfaces

Science.gov (United States)

Krajczewski, Jan; Kołątaj, Karol; Pietrasik, Sylwia; Kudelski, Andrzej

2018-03-01

One of the tools used for determining the composition of surfaces of various materials is shell-isolated nanoparticle-enhanced Raman spectroscopy (SHINERS). SHINERS is a modification of "standard" surface-enhanced Raman spectroscopy (SERS), in which, before Raman spectra are recorded, the surfaces analysed are covered with a layer of plasmonic nanoparticles protected by a very thin layer of a transparent dielectric. The plasmonic cores of the core-shell nanoparticles used in SHINERS measurements generate a local enhancement of the electric field of the incident electromagnetic radiation, whereas the transparent coatings prevent the metal cores from coming into direct contact with the material being analysed. In this contribution, we propose a new type of SHINERS nanoresonators that contain spiky, star-shaped metal cores (produced from a gold/silver alloy). These spiky, star-shaped Au-Ag nanoparticles have been covered by a layer of silica. The small radii of the ends of the tips of the spikes of these plasmonic nanostructures make it possible to generate a very large enhancement of the electromagnetic field there, with the result that such SHINERS nanoresonators are significantly more efficient than the standard semi-spherical nanostructures. The Au-Ag alloy nanoparticles were synthesised by the reduction of a solution containing silver nitrate and chloroauric acid by ascorbic acid. The final geometry of the nanostructures thus formed was controlled by changing the ratio between the concentrations of AuCl4- and Ag+ ions. The shape of the synthesised star-shaped Au-Ag nanoparticles does not change significantly during the two standard procedures for depositing a layer of silica (by the decomposition of sodium silicate or the decomposition of tetraethyl orthosilicate).

Ag/Au/Polypyrrole Core-shell Nanowire Network for Transparent, Stretchable and Flexible Supercapacitor in Wearable Energy Devices

Science.gov (United States)

Moon, Hyunjin; Lee, Habeom; Kwon, Jinhyeong; Suh, Young Duk; Kim, Dong Kwan; Ha, Inho; Yeo, Junyeob; Hong, Sukjoon; Ko, Seung Hwan

2017-02-01

Transparent and stretchable energy storage devices have attracted significant interest due to their potential to be applied to biocompatible and wearable electronics. Supercapacitors that use the reversible faradaic redox reaction of conducting polymer have a higher specific capacitance as compared with electrical double-layer capacitors. Typically, the conducting polymer electrode is fabricated through direct electropolymerization on the current collector. However, no research have been conducted on metal nanowires as current collectors for the direct electropolymerization, even though the metal nanowire network structure has proven to be superior as a transparent, flexible, and stretchable electrode platform because the conducting polymer’s redox potential for polymerization is higher than that of widely studied metal nanowires such as silver and copper. In this study, we demonstrated a highly transparent and stretchable supercapacitor by developing Ag/Au/Polypyrrole core-shell nanowire networks as electrode by coating the surface of Ag NWs with a thin layer of gold, which provide higher redox potential than the electropolymerizable monomer. The Ag/Au/Polypyrrole core-shell nanowire networks demonstrated superior mechanical stability under various mechanical bending and stretching. In addition, proposed supercapacitors showed fine optical transmittance together with fivefold improved areal capacitance compared to pristine Ag/Au core-shell nanowire mesh-based supercapacitors.

Autoclave mediated one-pot-one-minute synthesis of AgNPs and Au-Ag nanocomposite from Melia azedarach bark extract with antimicrobial activity against food pathogens.

Science.gov (United States)

Pani, Alok; Lee, Joong Hee; Yun, Soon-Ii

2016-01-01

The increasing use of nanoparticles and nanocomposite in pharmaceutical and processed food industry have increased the demand for nontoxic and inert metallic nanostructures. Chemical and physical method of synthesis of nanostructures is most popular in industrial production, despite the fact that these methods are labor intensive and/or generate toxic effluents. There has been an increasing demand for rapid, ecofriendly and relatively cheaper synthesis of nanostructures. Here, we propose a strategy, for one-minute green synthesis of AgNPs and a one-pot one-minute green synthesis of Au-Ag nanocomposite, using Melia azedarach bark aqueous extract as reducing agent. The hydrothermal mechanism of the autoclave technology has been successfully used in this study to accelerate the nucleation and growth of nano-crystals. The study also presents high antimicrobial potential of the synthesized nano solutions against common food and water born pathogens. The multistep characterization and analysis of the synthesized nanomaterial samples, using UV-visible spectroscopy, ICP-MS, FT-IR, EDX, XRD, HR-TEM and FE-SEM, also reveal the reaction dynamics of AgNO3, AuCl3 and plant extract in synthesis of the nanoparticles and nanocomposite. The antimicrobial effectiveness of the synthesized Au-Ag nanocomposite, with high gold to silver ratio, reduces the dependency on the AgNPs, which is considered to be environmentally more toxic than the gold counterpart. We hope that this new strategy will change the present course of green synthesis. The rapidity of synthesis will also help in industrial scale green production of nanostructures using Melia azedarach.

Photoemission studies of zinc-noble metal alloys: Zn--Cu, Zn--Ag, and Zn--Au films on Ru(001)

International Nuclear Information System (INIS)

Rodriguez, J.A.; Hrbek, J.

1993-01-01

Zn and the noble metals alloy when coadsorbed on Ru(001). The properties of Zn--Cu, Zn--Ag, and Zn--Au alloys have been studied using core- and valence-level photoemission and temperature programmed desorption. Alloy formation induces only small shifts (-0.2 to -0.3 eV) in the position of the Zn 2p, 3s, and 3d levels. In contrast, the core and valence levels of the noble metals show large shifts toward higher binding energy. For small amounts of Cu, Ag, and Au dissolved in Zn multilayers, the shifts in the core levels of the nobel metals follow the sequence: Cu(2p 3/2 ), 0.8 eV∼Ag(3d 5/2 ), 0.8 eV 7/2 ), 1.4 eV. The magnitude of the shift increases as the Pauling electronegativity of the noble metal increases. However, the sign of the shifts for the Cu(2p 3/2 ), Ag(3d 5/2 ), or Au(4f 7/2 ) levels is not directly determined by the direction of charge transfer within the corresponding Zn-noble metal bond

Characterization of electroless Au, Pt and Pd contacts on CdTe and ZnTe by RBS and SIMS techniques

Energy Technology Data Exchange (ETDEWEB)

Roumie, M. E-mail: mroumie@cnrs.edu.lb; Hageali, M.; Zahraman, K.; Nsouli, B.; Younes, G

2004-06-01

Rutherford backscattering spectrometry (RBS) was applied to characterize Au, Pt and Pd contacts on II-VI semiconductor materials, CdTe and ZnTe, used as nuclear detectors. Electroless thin film depositions were prepared by changing the concentration of the reaction solution. Contrary to the deposition reaction time, it was observed that the amount of solution dilution degree had a considerable effect on increasing the thickness of the metal layer. Furthermore, PICTS electrical measurements confirmed the depth profile analysis performed by RBS and SIMS.

Hubungan Kondisi Geologi terhadap Alterasi dan Mineralisasi Endapan Epithermal Daerah Sualan, Kecamatan Talegong, Kabupaten Garut, Provinsi Jawa Barat

OpenAIRE

Kumala Sari, Paramitha Eka

2013-01-01

In exploration process of epithermal deposit, it is important to understand alteration and mineralization. The presence of alteration and mineralization zones help development of ore mineral exploration. Hydrothermal alteration is change of the chemistry, physics, mineralogy and origin textures of rocks as it interacts with the hydrothermal fluid. Alteration and mineralization zones has characteristics and certain minerals in each area.The research purposes are to determine the geological ...

Physicochemical properties of new As2Se3–Ag4SSe–CdTe glasses

International Nuclear Information System (INIS)

Aljihmani, Lilia; Vassilev, Venceslav; Hristova-Vasileva, Temenuga; Fidancevska, Emilija

2009-01-01

Chalcogenide glasses from the As 2 Se 3 –Ag 4 SSe–CdTe system were synthesized. The basic physicochemical parameters such as density (d), microhardness (HV) and the temperatures glass transition Tg were measured. Compactness (C) and some thermomechanical characteristics such as volume (Vh) and formation energy (Eh) of micro-voids in the glassy network, as well as the module of elasticity (E) were calculated. A correlation between the composition and properties of the As 2 Se 3 –Ag 4 SSe–CdTe glasses was established and comprehensively discussed. Keywords: chalcogenide glasses, density, microhardness, compactness, elasticity modulus, thermomechanical characteristics

Martensitic transformation behavior in Ti–Ni–X (Ag, In, Sn, Sb, Te, Tl, Pb, Bi) ternary alloys

Energy Technology Data Exchange (ETDEWEB)

Jang, Jai-young; Chun, Su-jin; Kim, Nam-suk; Cho, Jeung-won; Kim, Jae-hyun [School of Materials Science and Engineering, Gyeongsang National University, 900 Gazwadong, Jinju, Gyeongnam 660-701 (Korea, Republic of); Yeom, Jong-taek [Light Metal Division, Korea Institute of Materials Science (KIMS), Changwon 642-831 (Korea, Republic of); Kim, Jae-il [Materials Science and Engineering, University of Dong-A, Hadan-dong, Saha-gu, Busan 604-714 (Korea, Republic of); Nam, Tae-hyun, E-mail: tahynam@gnu.ac.kr [School of Materials Science and Engineering, Gyeongsang National University, 900 Gazwadong, Jinju, Gyeongnam 660-701 (Korea, Republic of)

2013-12-15

Graphical abstract: - Highlights: • Ag, In and Sn were soluble in TiNi matrix, while Sb, Te, Tl, Pb and Bi were not. • The B2-R-B19′transformation occurred in Ti-Ni-(Ag, In, Sn) alloys. • Solid solution hardening was essential for inducing the B2-R transformation. - Abstract: The microstructures and transformation behaviors of Ti–Ni–X (Ag, In, Sn, Sb, Te, Tl, Pb, Bi) ternary alloys were investigated using electron probe micro-analysis (EPMA), X-ray diffraction (XRD), differential scanning calorimetry (DSC) and Micro Vickers hardness tests. All specimens consisted of Ti–Ni matrices and second phase particles. Ag, In and Sn were soluble in Ti–Ni matrices with a limited solubility (≤1.0 at%), while Sb, Te, Tl, Pb and Bi were not soluble. Two-stage B2-R-B19′ transformation occurred in Ti–48.8Ni–1.2Ag, Ti–49.0Ni–1.0In and Ti–49.0Ni–1.0Sn alloys, while one-stage B2-B19′ transformation occurred in Ti–49.0Ni–1.0Ag, Ti–49.0Ni–1.0Sb, Ti–49.0Ni–1.0Te, Ti–49.0Ni–1.0Pb and Ti–49.0Ni–1.0Bi alloys. Micro Vickers hardness of the alloys displaying the B2-R-B19′ transformation (Hv 250–368) was much larger than that (

Martensitic transformation behavior in Ti–Ni–X (Ag, In, Sn, Sb, Te, Tl, Pb, Bi) ternary alloys

International Nuclear Information System (INIS)

Jang, Jai-young; Chun, Su-jin; Kim, Nam-suk; Cho, Jeung-won; Kim, Jae-hyun; Yeom, Jong-taek; Kim, Jae-il; Nam, Tae-hyun

2013-01-01

Graphical abstract: - Highlights: • Ag, In and Sn were soluble in TiNi matrix, while Sb, Te, Tl, Pb and Bi were not. • The B2-R-B19′transformation occurred in Ti-Ni-(Ag, In, Sn) alloys. • Solid solution hardening was essential for inducing the B2-R transformation. - Abstract: The microstructures and transformation behaviors of Ti–Ni–X (Ag, In, Sn, Sb, Te, Tl, Pb, Bi) ternary alloys were investigated using electron probe micro-analysis (EPMA), X-ray diffraction (XRD), differential scanning calorimetry (DSC) and Micro Vickers hardness tests. All specimens consisted of Ti–Ni matrices and second phase particles. Ag, In and Sn were soluble in Ti–Ni matrices with a limited solubility (≤1.0 at%), while Sb, Te, Tl, Pb and Bi were not soluble. Two-stage B2-R-B19′ transformation occurred in Ti–48.8Ni–1.2Ag, Ti–49.0Ni–1.0In and Ti–49.0Ni–1.0Sn alloys, while one-stage B2-B19′ transformation occurred in Ti–49.0Ni–1.0Ag, Ti–49.0Ni–1.0Sb, Ti–49.0Ni–1.0Te, Ti–49.0Ni–1.0Pb and Ti–49.0Ni–1.0Bi alloys. Micro Vickers hardness of the alloys displaying the B2-R-B19′ transformation (Hv 250–368) was much larger than that (< Hv 200) of the alloys displaying the B2-B19′ transformation. Solid solution hardening was an important factor for inducing the B2-R transformation in Ti–Ni–X (X = non-transition elements) alloys

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

Science.gov (United States)

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.

Suivie de diabète gestationnel au service de la maternité Tlemcen

OpenAIRE

Djadoudi, Ahlam

2015-01-01

Les grossesses compliquées d‟un diabète soit préexistant, soit apparu au Cours de la grossesse « diabète gestationnel », restent des grossesses à risque de complications materno-foetales. La présence d‟un diabète préexistant confère un risque surajouté de malformations foetales. La pathogénie de ces complications fait largement intervenir l‟hyperglycémie, d‟autres facteurs encore mal connus pourraient aussi être impliqués. De part sa fréquence et ses risques encourus par la mère et l‟en...

Electrochemical Glucose Oxidation Using Glassy Carbon Electrodes Modified with Au-Ag Nanoparticles: Influence of Ag Content

Directory of Open Access Journals (Sweden)

Nancy Gabriela García-Morales

2015-01-01

Full Text Available This paper describes the application of glassy carbon modified electrodes bearing Aux-Agy nanoparticles to catalyze the electrochemical oxidation of glucose. In particular, the paper shows the influence of the Ag content on this oxidation process. A simple method was applied to prepare the nanoparticles, which were characterized by transmission electron microscopy, Ultraviolet-Visible spectroscopy, X-ray diffraction spectroscopy, and cyclic voltammetry. These nanoparticles were used to modify glassy carbon electrodes. The effectiveness of these electrodes for electrochemical glucose oxidation was evaluated. The modified glassy carbon electrodes are highly sensitive to glucose oxidation in alkaline media, which could be attributed to the presence of Aux-Agy nanoparticles on the electrode surface. The voltammetric results suggest that the glucose oxidation speed is controlled by the glucose diffusion to the electrode surface. These results also show that the catalytic activity of the electrodes depends on the Ag content of the nanoparticles. Best results were obtained for the Au80-Ag20 nanoparticles modified electrode. This electrode could be used for Gluconic acid (GA production.

130 MeV Au ion irradiation induced dewetting on In{sub 2}Te{sub 3} thin film

Energy Technology Data Exchange (ETDEWEB)

Matheswaran, P.; Abhirami, K.M.; Gokul, B. [Department of Physics, Kongunadu Arts and Science College, Coimbatore 641029 (India); Sathyamoorthy, R., E-mail: rsathya1959@gmail.com [Department of Physics, Kongunadu Arts and Science College, Coimbatore 641029 (India); Prakash, Jai [Department of Chemistry, M.M.H. College, Ghaziabad 201001 (India); Asokan, K.; Kanjilal, D. [Materials Science Division, Inter University Accelerator Centre, New Delhi 110067 (India)

2012-09-01

Highlights: Black-Right-Pointing-Pointer In{sub 2}Te{sub 3} phase formed from In/Te bilayer by 130 MeV Au ion irradiation. Black-Right-Pointing-Pointer Lower fluence results mixed phases with initial state of dewetting. Black-Right-Pointing-Pointer At higher fluence, In{sub 2}Te{sub 3} phase with complete dewetting pattern is formed. Black-Right-Pointing-Pointer Thermal spike model is used to explain the inter face mixing phenomena. Black-Right-Pointing-Pointer SHI irradiation may be used to functionalize the structural and surface properties of thin films. - Abstract: In/Te bilayer thin films were prepared by sequential thermal evaporation and subsequently irradiated by 130 MeV Au ions. The pristine and irradiated samples were characterized by X-ray diffraction (XRD), Rutherford backscattering spectrometry (RBS), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX) techniques. RBS spectra reveal the sputtering of Te film and interface mixing, with increasing fluence. The surface morphology showed the beginning of dewetting of Te thin film and formation of the partially connected with the mixed zones at the fluence of 1 Multiplication-Sign 10{sup 13} ions/cm{sup 2}. At the higher fluence of 3 Multiplication-Sign 10{sup 13} ions/cm{sup 2}, dewetted structures were isolated at the surface. Above results are explained based on the formation of craters, sputtering and dewetting followed by inter-diffusion at the interface of molten zones due to thermal spike induced by Au ions.

Diffusion of Ag, Au and Cs implants in MAX phase Ti{sub 3}SiC{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Jiang, Weilin, E-mail: weilin.jiang@pnnl.gov [Pacific Northwest National Laboratory, Richland, WA (United States); Henager, Charles H.; Varga, Tamas; Jung, Hee Joon; Overman, Nicole R. [Pacific Northwest National Laboratory, Richland, WA (United States); Zhang, Chonghong; Gou, Jie [Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou (China)

2015-07-15

MAX phases (M: early transition metal; A: elements in group 13 or 14; X: C or N), such as titanium silicon carbide (Ti{sub 3}SiC{sub 2}), have a unique combination of both metallic and ceramic properties, which make them attractive for potential nuclear applications. Ti{sub 3}SiC{sub 2} has been considered as a possible fuel cladding material. This study reports on the diffusivities of fission product surrogates (Ag and Cs) and a noble metal Au (with diffusion behavior similar to Ag) in this ternary compound at elevated temperatures, as well as in dual-phase nanocomposite of Ti{sub 3}SiC{sub 2}/3C-SiC and polycrystalline CVD 3C-SiC for behavior comparisons. Samples were implanted with Ag, Au or Cs ions and characterized with various methods, including X-ray diffraction, electron backscatter diffraction, energy dispersive X-ray spectroscopy, Rutherford backscattering spectrometry, helium ion microscopy, and transmission electron microscopy. The results show that in contrast to immobile Ag in 3C-SiC, there is a significant outward diffusion of Ag in Ti{sub 3}SiC{sub 2} within the dual-phase nanocomposite during Ag ion implantation at 873 K. Similar behavior of Au in polycrystalline Ti{sub 3}SiC{sub 2} was also observed. Cs out-diffusion and release from Ti{sub 3}SiC{sub 2} occurred during post-implantation thermal annealing at 973 K. This study suggests caution and further studies in consideration of Ti{sub 3}SiC{sub 2} as a fuel cladding material for advanced nuclear reactors operating at very high temperatures.

Silica-covered star-shaped Au-Ag nanoparticles as new electromagnetic nanoresonators for Raman characterisation of surfaces.

Science.gov (United States)

Krajczewski, Jan; Kołątaj, Karol; Pietrasik, Sylwia; Kudelski, Andrzej

2018-03-15

One of the tools used for determining the composition of surfaces of various materials is shell-isolated nanoparticle-enhanced Raman spectroscopy (SHINERS). SHINERS is a modification of "standard" surface-enhanced Raman spectroscopy (SERS), in which, before Raman spectra are recorded, the surfaces analysed are covered with a layer of plasmonic nanoparticles protected by a very thin layer of a transparent dielectric. The plasmonic cores of the core-shell nanoparticles used in SHINERS measurements generate a local enhancement of the electric field of the incident electromagnetic radiation, whereas the transparent coatings prevent the metal cores from coming into direct contact with the material being analysed. In this contribution, we propose a new type of SHINERS nanoresonators that contain spiky, star-shaped metal cores (produced from a gold/silver alloy). These spiky, star-shaped Au-Ag nanoparticles have been covered by a layer of silica. The small radii of the ends of the tips of the spikes of these plasmonic nanostructures make it possible to generate a very large enhancement of the electromagnetic field there, with the result that such SHINERS nanoresonators are significantly more efficient than the standard semi-spherical nanostructures. The Au-Ag alloy nanoparticles were synthesised by the reduction of a solution containing silver nitrate and chloroauric acid by ascorbic acid. The final geometry of the nanostructures thus formed was controlled by changing the ratio between the concentrations of AuCl 4 - and Ag + ions. The shape of the synthesised star-shaped Au-Ag nanoparticles does not change significantly during the two standard procedures for depositing a layer of silica (by the decomposition of sodium silicate or the decomposition of tetraethyl orthosilicate). Copyright © 2017 Elsevier B.V. All rights reserved.

Insight into the electronic structure of the supramolecular “rods-in-belt” Au{sup I}-Cu{sup I} and Au{sup I}-Ag{sup I} self-assembled complexes from X-ray photoelectron and absorption spectroscopy

Energy Technology Data Exchange (ETDEWEB)

Makarova, Anna A. [Department of Physics, St. Petersburg State University, St. Petersburg 198504 (Russian Federation); Institut für Festkörperphysik, Technische Universität Dresden, D-01062 Dresden (Germany); Grachova, Elena V.; Krupenya, Dmitry V. [Department of Chemistry, St. Petersburg State University, St. Petersburg 198504 (Russian Federation); Vilkov, Oleg [Department of Physics, St. Petersburg State University, St. Petersburg 198504 (Russian Federation); Institut für Festkörperphysik, Technische Universität Dresden, D-01062 Dresden (Germany); Fedorov, Alexander [Department of Physics, St. Petersburg State University, St. Petersburg 198504 (Russian Federation); Leibniz-Institut für Festkörper- und Werkstoffforschung Dresden, Dresden (Germany); Usachov, Dmitry [Department of Physics, St. Petersburg State University, St. Petersburg 198504 (Russian Federation); Generalov, Alexander [Department of Physics, St. Petersburg State University, St. Petersburg 198504 (Russian Federation); Institut für Festkörperphysik, Technische Universität Dresden, D-01062 Dresden (Germany); Koshevoy, Igor O. [Department of Chemistry, St. Petersburg State University, St. Petersburg 198504 (Russian Federation); Department of Chemistry, University of Eastern Finland, Joensuu 80101 (Finland); Tunik, Sergey P. [Department of Chemistry, St. Petersburg State University, St. Petersburg 198504 (Russian Federation); Rühl, Eckart [Physikalische Chemie, Institut für Chemie und Biochemie Freie Universität Berlin (Germany); and others

2014-01-01

Highlights: • Electronic structure of rods-in-belt complexes was described via PES and NEXAFS. • With increasing size the molecule becomes more sensitive to X-ray damage effects. • The HOMO consists of a combination of the d-Cu/Ag and π-C≡C states. • HOMOs are positioned at about 2.2 eV for Au-Cu and 2.5 eV BE for Au-Ag complexes. • LUMOs are located on the C-skeleton including π*-C≡C and π*-C=C{sub aromatic} orbitals. - Abstract: The recently discovered “rods-in-belt” supramolecular complexes with Au-Cu or Au-Ag cluster cores exhibit self-assembly behavior, have a very unusual structural motif, and what is most important, show remarkable light emitting properties. The electronic and photophysical characteristics of these unique objects can be relatively easy tuned by modifying the ligand (alkynyl and phosphine) environment. Because of these properties the “rods-in-belt” supramolecules could serve as building blocks for next generation electronics, and in particular, for light-emitting devices and in bioimaging applications. Herein, we report a comprehensive characterization of the electronic structure of two families of alkynyl-diphosphine supramolecular complexes with the heterometallic Au-Cu and Au-Ag cores. Using X-ray photoemission and absorption spectroscopy we disentangled the structure of their occupied and unoccupied electronic states close to the Fermi level. The results obtained suggest that the major contribution to the highest occupied molecular orbitals is made by the triple bonded carbons hosted in the dialkynyl-gold “rods” and the copper (silver) atoms from the central cluster core of the heterometallic Au-Cu (Au-Ag) molecules. The lowest unoccupied molecular orbitals are located on the carbon skeleton of the complexes and include π*-C≡C and π*-C=C{sub aromatic} orbitals. The onset of the valence band in the Au-Ag systems starts at about 0.3 eV lower than that in the Au-Cu complexes, implying a slightly larger energy

Results of LA-ICP-MS sulfide mapping from Algoma-type BIF gold systems with implications for the nature of mineralizing fluids, metal sources, and deposit models

Science.gov (United States)

Gourcerol, B.; Kontak, D. J.; Thurston, P. C.; Petrus, J. A.

2018-01-01

Quantitative laser ablation inductively coupled plasma-mass spectrometry (LA-ICP-MS) element distribution maps combined with traverse mode analyses have been acquired on various sulfides (pyrite, pyrrhotite, arsenopyrite) from three Canadian Algoma-type BIF-hosted gold deposits ( 4 Moz Au Meadowbank, ≥ 2.8 Moz Au Meliadine district, 6 Moz Au Musselwhite). These data, in conjunction with detailed petrographic and SEM-EDS observations, provide insight into the nature and relative timing of gold events, the presence and implication of trace element zoning regarding crystallization processes, and elemental associations that fingerprint gold events. Furthermore, the use of an innovative method of processing the LA-ICP-MS data in map and traverse modes, whereby the results are fragmented into time-slice data, to generate various binary plots (Ag versus Ni) provides a means to identify elemental associations (Te, Bi) not otherwise apparent. This integrated means of treating geochemical data, along with petrography, allows multiple gold events and remobilization processes to be recognized and their elemental associations determined. The main gold event in each of these deposits is characterized by the coupling of an As-Se-Te-Ag element association coincident with intense stratabound sulfide-replacement of the Fe-rich host rock. Additionally, the data indicate presence of a later remobilization event, which upgraded the Au tenor, as either non-refractory or refractory type, along fracture networks due to the ingress of subsequent base metal-bearing metamorphic fluids (mainly a Pb-Bi association). Furthermore, the data reveal a stratigraphic influence, as reflected in the elemental associations and the elemental enrichments observed and the nature of the sulfide phase hosting the gold mineralization (arsenopyrite versus pyrite).

Improvement in grade of minerals using simultaneous Bio-oxidation of invisible gold concentrate and deep-sea manganese crust

Science.gov (United States)

Myung, EunJi; Cho, Kang Hee; Kim, Hyun Soo; Park, Cheon Young

2016-04-01

Many sulfides of metal such as galena, sphalerite, chalcopyrite, and pyrite, are semiconductors. When two kinds of such minerals contact each other in an electrolyte, a galvanic couple, where the mineral of lower rest potential as anode, and that of higher rest potential as cathode forms. Manganese dioxide is also a semiconductor with much higher rest potential than all sulfides mentioned above, so that a galvanic couple in which both the minerals would dissolve simultaneously can form, when it contacts with any of the sulfides. The aim of this study was to investigate the improvement in grade of minerals using the simultaneous bio-oxidation of deep-sea manganese crust and invisible gold concentrate. The samples(deep-sea manganese crust and invisible gold concentrate) were characterized by chemical and XRD analysis. The primary components of the invisible gold concentrate was pyrite and quartz and the deep-sea manganese crust was amorphous material, as detected using XRD. The result of chemical analysis showed that Au, Ag, Te contents in the invisible gold concentrate 130.2, 954.1 and 1,043.6 mg/kg, respectively. and that Mn, Ni, Co contents in the deep-sea manganese crust 19,501.5, 151.9, 400.4 mg/kg, respectively. In order to increase the bacteria's tolerance of heavy metals, the bacteria using bio-oxidation experiments were repeatedly subcultured in an Cu adaptation-medium containing of 382.98 mg/l for 20 periods of 21 days. The improvement in grade of samples of in present adapted bacteria condition was greater than another conditions(control and in present non-adapted bacteria). The Au-Ag-Te contents in the invisible gold concentrate was enhanced in the order of physical oxidation, simultaneous/non-adaptive bio-oxidation, adaptive/bio-oxidation, simultaneous/adaptive bio-oxidation. If the bacteria is adapted to heavy metal ions and an optimization of conditions is found in future bio-oxidation-leaching processes. Acknowledgment : "This research was supported

Changes in the microbiological and chemical characteristics of white bread during storage in paper packages modified with Ag/TiO2-SiO2, Ag/N-TiO2 or Au/TiO2.

Science.gov (United States)

Peter, Anca; Mihaly-Cozmuta, Leonard; Mihaly-Cozmuta, Anca; Nicula, Camelia; Ziemkowska, Wanda; Basiak, Dariusz; Danciu, Virginia; Vulpoi, Adriana; Baia, Lucian; Falup, Anca; Craciun, Grigore; Ciric, Alexandru; Begea, Mihaela; Kiss, Claudia; Vatuiu, Daniela

2016-04-15

Microbiological and chemical characteristics of white bread during storage in paper-packages modified with Ag/TiO2-SiO2, Ag/N-TiO2 or Au/TiO2 were investigated. The whiteness and the water retention of the modified packages were slightly superior to those exhibited by the reference sample, as the color of the composite was lighter. The water retention was very good especially for the Ag/TiO2-SiO2-paper. These improvements can be associated with the high specific surface area and with the low agglomeration tendency of Ag nanoparticles in comparison with the Au ones. The preservation activity of the composites for the bread storage is positively influenced by photoactivity and presence of nano-Ag. Packages Ag/TiO2-SiO2-paper and Ag/N-TiO2-paper can find their applicability for extending the shelf life of bread by 2 days as compared with the unmodified paper-package. No influence of the Au/TiO2 on the extending the shelf life of bread was observed. Copyright © 2015 Elsevier Ltd. All rights reserved.

Geology, geochemistry and fluid inclusion of Qarachilar Cu-Mo-Au quartz veins, northeast of Kharvana, East Azerbaijan

Directory of Open Access Journals (Sweden)

Fariba Asiay Soufiani

2018-04-01

Full Text Available Introduction The Qarachilar Cu-Mo-Au occurrence is located in the Arasbaran ore zone (AZ, NW Iran, some 70 km north of Tabriz. The AZ is characterized by occurrence of different types of mineralization and hosts many Cu-Mo porphyry (PCD, Cu skarn, and epithermal Au deposits (Jamali et al., 2010; Jamali and Mehrabi, 2015. The main rock unit exposed in the area is Qaradagh batholith (QDB. A variety of porphyry and vein-type Cu–Mo–Au mineralization are associated with QDB. The most pronounced occurrences are in Qarachilar, Qara-Dareh, Zarli-Dareh, Aniq and Pirbolagh. This type of mineralization can be followed in other parts of northwest Iran, such as Masjed-Daghi porphyry Cu–Au deposit and Mivehrood vein-type Au mineralization in the southwest of the QDB, the Sungun PCD and the related skarn in its southeast, and Astamal Fe skarn deposit in the south of the QDB. To date, no detailed study has been undertaken to understand the characteristics of the Qarachilar occurrence and its mineralization type is controversial. The recent work by Simmonds and Moazzen (2015 also did not present relevant information for an understanding of the Qarachilar occurrence. The Re–Os age data obtained in their work were compared with similar events along the Urumieh-Dokhtar magmatic arc (UDMA and southern Lesser Caucasus in order to elucidate the temporal pattern of mineralization across the whole QDB and the UDMA. The present paper provides an overview of the geological framework, the mineralization characteristics, and the results of geochemistry and fluid inclusion studies of the Qarachilar Cu-Mo-Au occurrence with an application to the ore genesis. Materials and methods More than 37 polished thin sections from Qarachilar host rocks and mineralized and altered zones were studied by conventional petrographic and mineralogic methods at the University of Zanjan. In addition, 9 samples from non-altered and altered host rocks and mineralized veins were analyzed by

A preliminary inter-centre comparison study for photon, thermal neutron and epithermal neutron responses of two pairs of ionisation chambers used for BNCT

International Nuclear Information System (INIS)

Roca, Antoaneta; Liu, Yuan-Hao; Wojnecki, Cecile; Green, Stuart; Nievaart, Sander; Ghani, Zamir; Moss, Ray

2009-01-01

The dual ionisation chamber technique is the recommended method for mixed field dosimetry of epithermal neutron beams. This paper presents initial data from an ongoing inter-comparison study involving two identical pairs of ionisation chambers used at the BNCT facilities of Petten, NL and of University of Birmingham, UK. The goal of this study is to evaluate the photon, thermal neutron and epithermal neutron responses of both pairs of TE(TE) (Exradin T2 type) and Mg(Ar) (Exradin M2 type) ionisation chambers in similar experimental conditions. At this stage, the work has been completed for the M2 type chambers and is intended to be completed for the T2 type chambers in the near future.

Soft phonon modes leading to ultralow thermal conductivity and high thermoelectric performance in AgCuTe

Energy Technology Data Exchange (ETDEWEB)

Roychowdhury, Subhajit; Jana, Manoj K.; Pan, Jaysree; Guin, Satya N.; Waghmare, Umesh V.; Biswas, Kanishka [New Chemistry Unit and Theoretical Science Unit, Jawaharlal Nehru Centre for Advanced Scientific Research (JNCASR), Bangalore (India); Sanyal, Dirtha [Variable Energy Cyclotron Centre, 1/AF Bidhannagar, Kolkata (India)

2018-04-03

Crystalline solids with intrinsically low lattice thermal conductivity (κ{sub L}) are crucial to realizing high-performance thermoelectric (TE) materials. Herein, we show an ultralow κ{sub L} of 0.35 Wm{sup -1} K{sup -1} in AgCuTe, which has a remarkable TE figure-of-merit, zT of 1.6 at 670 K when alloyed with 10 mol % Se. First-principles DFT calculation reveals several soft phonon modes in its room-temperature hexagonal phase, which are also evident from low-temperature heat-capacity measurement. These phonon modes, dominated by Ag vibrations, soften further with temperature giving a dynamic cation disorder and driving the superionic transition. Intrinsic factors cause an ultralow κ{sub L} in the room-temperature hexagonal phase, while the dynamic disorder of Ag/Cu cations leads to reduced phonon frequencies and mean free paths in the high-temperature rocksalt phase. Despite the cation disorder at elevated temperatures, the crystalline conduits of the rigid anion sublattice give a high power factor. (copyright 2018 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

Phenomenological approach to the spin glass state of (Cu-Mn, Ag-Mn, Au-Mn and Au-Fe) alloys at low temperatures

International Nuclear Information System (INIS)

Al-Jalali, Muhammad A.; Kayali, Fawaz A.

2000-01-01

Full text.The spin glass of: (Cu-Mn, Ag-Mn, Au-Mn, Au-Fe) alloys has been extensively studied. The availability of published and assured experimental data on the susceptibility x(T) of this alloys has enabled the design and application of phenomenological approach to the spin glass state of these interesting alloys. The use of and advanced (S.P.S.S) computer software has resulted revealing some important features of the spin glass in these alloys, the most important of which is that the spin glass state do not represent as phase change

Electronic energy loss of low velocity H+ beams in Al, Ag, Sb, Au and Bi

International Nuclear Information System (INIS)

Valdes, J.E.; Martinez Tamayo, G.; Lantschner, G.H.; Eckardt, J.C.; Arista, N.R.

1993-01-01

The energy loss of H + ions in thin polycrystalline Al, Sb, Ag, Au and Bi films has been determined in the energy range below 10 keV. This low-energy range is of special interest to fill a lack of low-energy experimental data and test various theoretical predictions and semiempirical formulas. We find that the general theoretical prediction of a velocity-proportional dependence of energy loss does not hold for all targets studied in this work. The velocity-proportionality is better satisfied for Al, Sb and Bi, whereas a departure from such dependence is observed at lower energies for Ag and Au targets. The results obtained here are in good general agreement with nonlinear stopping power calculations based on density functional theory. Comparison with semiempirical predictions, and other experimental results are also done. (orig.)

Directed flow and particle production in Au+Au collisions from experiment E877 at the AGS

International Nuclear Information System (INIS)

Barrette, J.

1996-01-01

In this article we summarize recent results on the study of Au+Au collisions at 10.8A GeV/c obtained at the AGS by the E877 Collaboration. New results on the directed sideward flow are presented. In particular, the dependence of proton and pion production on the direction of the reaction plane will be discussed. It is shown that the sideward flow is mainly due to nucleons and that pions show little flow effects. Two-pion correlation functions are studied to derive the density at freeze-out. Further, we inspect the correlations as a function of the pion direction relative to the reaction plane. A dependence of the deduced source sizes on the pair direction and momentum is observed. The measured source sizes are compared to results obtained in lighter systems. Measured m t spectra of pions and kaons are also presented. The pion spectra show an enhancement at low m t similar to that observed in Si+Pb and which was attributed to triangle resonance excitation. However, in contrast to Si+Pb now a clear difference between the π + and π - spectra is seen. The K + spectra, which showed a very steep component over a small p t range in the previously studied Si+Pb reaction exhibit for Au+Au an unexpected structure at very low p t

OPTIMIZATION IN THE RECOVERY OF Au AND Ag VIA CYANIDATION OF FOUNDRY IN SLAG

Directory of Open Access Journals (Sweden)

Natalia Hidalgo

2014-03-01

Full Text Available This work aim was to recover and improvethe extraction of gold and silvercontained in the slag smelting, using the same metallurgical processes as in gold ores.The slag was concentrated in a centrifuge type Knelson, obtaining a(C1 concentrate and a (T1 tail. In order to optimize the recovery, an intensive T1 leaching was conducted. The variables used were: particle size, NaCN concentration (2000 to 4000 g/cm3 and aeration, with the residence time of 120 minutes. It is concluded that the recovery of Au, using gravity concentration (Knelson centrifuge is 83.6%, with Ag recovery of 52.5%. Au recovery is optimized to 90.4% by means of leaching tail centrifugal separation and 45.6% of Ag. The optimal conditions are: 4000 g/cm3of NaCN and artificial aeration, size [-14 # - # +35], in a lapse of 98 hours.

Equilibrium, kinetics and mechanism of Au3+, Pd2+ and Ag+ ions adsorption from aqueous solutions by graphene oxide functionalized persimmon tannin.

Science.gov (United States)

Wang, Zhongmin; Li, Xiaojuan; Liang, Haijun; Ning, Jingliang; Zhou, Zhide; Li, Guiyin

2017-10-01

In this study, a novel bio-adsorbent (PT-GO) was prepared by functionalization persimmon tannin (PT) with graphene oxide (GO) and the effective adsorption behaviors of Au 3+ , Pd 2+ and Ag + ions from aqueous solution was investigated. The PT-GO was characterized by Fourier transform infrared spectrometer (FTIR), scanning electronic microscope (SEM), thermogravimetric analysis (TGA) and Zeta potential. Many influence factors such as pH value, bio-adsorbent dosage, initial concentration of metal ions and contact time were optimized. The maximum adsorption capacity for Au 3+ , Pd 2+ and Ag + was 1325.09mg/g, 797.66mg/g and 421.01mg/g, respectively. The equilibrium isotherm for the adsorption of Au 3+ and Ag + on PT-GO were found to obey the Langmuir model, while the Freundlich model fitted better for Pd 2+ . The adsorption process of Au 3+ , Pd 2+ presented relatively fast adsorption kinetics with pseudo-second-order equation as the best fitting model, while the pseudo-first-order kinetic model was suitable for describing the adsorption of Ag + . Combination of ion exchange, electrostatic interaction and physical adsorption was the mechanism for adsorption of Au 3+ , Pd 2+ and Ag + onto PT-GO bio-adsorbent. Therefore, the PT-GO bio-adsorbent would be an ideal adsorbent for removal of precious metal ions and broaden the potential applications of persimmon tannin in environmental research. Copyright © 2017 Elsevier B.V. All rights reserved.

Directional epithermal neutron detector

International Nuclear Information System (INIS)

Givens, W.W.; Mills, W.R. Jr.

1986-01-01

A borehole tool for epithermal neutron die-away logging of subterranean formations surrounding a borehole is described which consists of: (a) a pulsed source of fast neutrons for irradiating the formations surrounding a borehole, (b) at least one neutron counter for counting epithermal neutrons returning to the borehole from the irradiated formations, (c) a neutron moderating material, (d) an outer thermal neutron shield providing a housing for the counter and the moderating material, (e) an inner thermal neutron shield dividing the housing so as to provide a first compartment bounded by the inner thermal neutron shield and a first portion of the outer thermal neutron shield and a second compartment bounded by the inner thermal neutron shield and a second portion of the outer thermal neutron shield, the counter being positioned within the first compartment and the moderating material being positioned within the second compartment, and (f) means for positioning the borehole tool against one side of the borehole wall and azimuthally orienting the borehole tool such that the first chamber is in juxtaposition with the borehole wall, the formation epithermal neutrons penetrating into the first chamber through the first portion of the outer thermal neutron shield are detected by the neutron counter for die-away measurement, thereby maximizing the directional sensitivty of the neutron counter to formation epithermal neutrons, the borehole fluid epithermal neutrons penetrating into the second chamber through the second chamber through the second portion of the outer thermal neutron shield are largely slowed down and lowered in energy by the moderating material and absorbed by the inner thermal neutron shield before penetrating into the first chamber, thereby minimizing the directional sensitivity of the neutron counter to borehole fluid epithermal neutrons

Installation and testing of an optimized epithermal neutron beam at the Brookhaven Medical Research Reactor (BMRR)

Energy Technology Data Exchange (ETDEWEB)

Fairchild, R.G.; Kalef-Ezra, J.; Saraf, S.K.; Fiarman, S.; Ramsey, E.; Wielopolski, L.; Laster, B.; Wheeler, F. (Brookhaven National Lab., Upton, NY (USA); Ioannina Univ. (Greece); Brookhaven National Lab., Upton, NY (USA); State Univ. of New York, Stony Brook, NY (USA). Health Science Center; Brookhaven National Lab., Upton, NY (USA); EG and G Idaho, Inc., Idaho Falls, ID (USA))

1989-01-01

Various calculations indicate that an optimized epithermal neutron beam can be produced by moderating fission neutrons either with a combination of Al and D{sub 2}O, or with Al{sub 2}O{sub 3}. We have designed, installed and tested an Al{sub 2}O{sub 3} moderated epithermal neutron beam at the Brookhaven Medical Research Reactor (BMRR). The epithermal neutron fluence rate of 1.8 {times} 10{sup 9} n/cm{sup 2}-sec produces a peak thermal neutron fluence rate of 1.9 to 2.8 {times} 10{sup 9} n/cm{sup 2}-sec in a tissue equivalent (TE) phantom head, depending on the configuration. Thus a single therapy treatment of 5 {times} 10{sup 12} n/cm{sup 2} can be delivered in 30--45 minutes. All irradiation times are given for a BMRR power of 3 MW, which is the highest power which can be delivered continuously. 18 refs., 8 figs., 4 tabs.

Durch intrinsische defekte induzierte uphill-diffusion von Ag und Cu in CdTe

CERN Document Server

Wagner, Frank

In the framework of the present thesis, the diffusion of Ag in CdTe was investigated by the radiotracer $^{111}$Ag. Thereby the focus was on the possibility to create a Ag flux from regions of low Ag concentration to regions of high Ag concentration (uphill diffusion). The experimentally observed diffusion profiles are explained in the framework of a thermodynamic diffusion model, taking into account the defect charge state and the defect interaction. The distribution of the charged defects produces a electric field, which leads to a drift of the charged defects. The experimental data are well explained assuming that Ag is incorporated interstitially and ionized (Agi$^{+}$). The Agi$^{+}$ concentration then reflects the profile of the Fermi level, which again is determined by the intrinsic defect distribution or, more precisely, the deviation from stoichiometry. On the basis of the experimental data it is possible to gather information on the thermodynamic properties of extrinsic as well as intrinsic defects....

Rapid Synthesis of Highly Monodisperse Au x Ag 1− x Alloy Nanoparticles via a Half-Seeding Approach

KAUST Repository

Chng, Ting Ting

2011-05-03

Gold-silver alloy AuxAg1-x is an important class of functional materials promising new applications across a wide array of technological fields. In this paper, we report a fast and facile synthetic protocol for preparation of highly monodisperse AuxAg1-x alloy nanoparticles in the size range of 3-6 nm. The precursors employed in this work are M(I)-alkanethiolates (M = Au and Ag), which can be easily prepared by mixing common chemicals such as HAuCl4 or AgNO3 with alkanethiols at room temperature. In this half-seeding approach, one of the M(I)-alkanethiolates is first heated and reduced in oleylamine solvent, and freshly formed metal clusters will then act as premature seeds on which both the first and second metals (from M(I)-alkanethiolates, M = Au and Ag) can grow accordingly without additional nucleation and thus achieve high monodispersity for product alloy nanoparticles. Unlike in other prevailing methods, both Au and Ag elements present in these solid precursors are in the same monovalent state and have identical supramolecular structures, which may lead to a more homogeneous reduction and complete interdiffusion at elevated reaction temperatures. When the M(I)-alkanethiolates are reduced to metallic forms, the detached alkanethiolate ligands will serve as capping agent to control the growth. More importantly, composition, particle size, and optical properties of AuxAg1-x alloy nanoparticles can be conveniently tuned with this approach. The optical limiting properties of the prepared particles have also been investigated at 532 and 1064 nm using 7 ns laser pulses, which reveals that the as-prepared alloy nanoparticles exhibit outstanding broadband optical limiting properties with low thresholds. © 2011 American Chemical Society.

Evolution of Ternary AuAgPd Nanoparticles by the Control of Temperature, Thickness, and Tri-Layer

Directory of Open Access Journals (Sweden)

Sundar Kunwar

2017-11-01

Full Text Available Metallic alloy nanoparticles (NPs possess great potential to enhance the optical, electronic, chemical, and magnetic properties for various applications by the control of morphology and elemental composition. This work presents the fabrication of ternary AuAgPd alloy nanostructures on sapphire (0001 via the solid-state dewetting of sputter-deposited tri-metallic layers. Based on the systematic control of temperature, thickness, and deposition order of tri-layers, the composite AuAgPd alloy nanoparticles (NPs with various shape, size, and density are demonstrated. The metallic tri-layers exhibit various stages of dewetting based on the increasing growth temperatures between 400 and 900 °C at 15 nm tri-layer film thickness. Specifically, the nucleation of tiny voids and hillocks, void coalescence, the growth and isolated nanoparticle formation, and the shape transformation with Ag sublimation are observed. With the reduced film thickness (6 nm, tiny alloy NPs with improved structural uniformity and spatial arrangement are obtained due to enhanced dewetting. The growth trend of alloy NPs is drastically altered by changing the deposition order of metallic tri-layers. The overall evolution is governed by the surface diffusion and inter-mixing of metallic atoms, Rayleigh-like instability, surface and interface energy minimization, and equilibrium state of the system. The UV-VIS-NIR reflectance spectra reveal the formation of an absorption band and reflectance maxima at specific wavelengths based on the morphology and composition of AuAgPd alloy NPs. In addition, Raman spectra analysis shows the modulation of intensity and peak position of natural vibration modes of sapphire (0001.

Effect of fluctuations on electron and phonon processes and thermodynamic parameters of Ag2Te and Ag2Se in the region of phase transition

International Nuclear Information System (INIS)

Aliev, S. A.; Aliev, F. F.

2008-01-01

Temperature dependences of electrical conductivity σ, thermoelectric power α, results of differential thermal analysis ΔT y , thermal conductivity χ, temperature conductivity κ, and heat capacity C p were studied in Ag 2 Te and Ag 2 Se semiconductors in the region of the phase transition. Two extrema are observed in the temperature dependence χ(T): a maximum in the region of the α' → β' transition and a minimum in the region of the β' → β transition; these extrema are caused by the similar dependence C p (T). It is shown that the α → α' and β' → β transitions are displacement transitions, while the α' → β' transition is of reconstruction type. It is established that the disorder parameter η in silver chalcogenides is highly smeared in the region of the phase transition; therefore, disordering of phases at the point of the phase transition is incomplete: 73, 62, and 48% in Ag 2 Te, Ag 2 Se, and Ag 2 S, respectively. The minimum volumes V ph for new phases are calculated; it is shown that the value of V ph in displacement transitions is larger than in the reconstruction-type transitions

Study of helium diffusion, implanted at a cyclotron, in face-centered cubic metals: Au, Ag and Al

International Nuclear Information System (INIS)

Sciani, V.

1985-01-01

Helium in metals is produced by nuclear reactions of energetic particles. In nuclear technology the interest on helium in metals is import, due to its production by (n, α) reaction. Because helium has extremely low solubility in metals, the precipitation in the form of filled bubbles at elevated temperatures occurs, which have detrimental effects on mechanical properties and may limit the lifetime of structural components. One typical example is the high temperature embrittlement. The nucleation and growth of the bubbles strongly depends on the mobility of the helium. This work presents the study of helium diffusion in Au, Ag and Al at temperatures above room temperature. The helium created by (n, α) reactions has been simulated by homogeneous alpha particles implantation in cyclotron, at room temperature, in specimens of thicknesses between 5 and 50 μm and helium concentration between 10 -3 to 10 ppm. After implantation, the specimens were dropped in a furnace in a UHV-chamber and the diffusion was measured by observing the He-release during linear and isothermal annealings. The occurence of free diffusion was comparing the dependence of release kinetics on helium concentration, sample thickness, time and heating rate to diffusion theory and is clearly separeted from agglomeration process. The diffusion constants of helium in Au, Ag and Al follow an Arrhenius behavior, with: Au:D o =10 -1.0 cm 2 /s ΔH=1.70eV Ag:D 0 =10 -1.2 cm 2 /s ΔH=1.51eV Al:D o =10 +0.5 cm 2 /s ΔH=1.40eV. The results are compared to self-diffusion and to the diffusion of other gases in these metals. Comparison with theoretical estimates favours the vacancy mechanism for helium diffusion in Au, Ag and Al. (author) [pt

Géochimie et métallogénie des veines à Ag-Pb-Zn du bassin de Purcell, Colombie-Britannique

OpenAIRE

Paiement, Jean-Philippe

2010-01-01

Le bassin du Belt-Purcell est connu pour le gîte de type SEDEX de Sullivan et ses veines à Ag-Pb-Zn. Les veines du bassin de Purcell sont classées en trois types : 1) riches en Pb-Zn composées de sphalérite, galène, pyrrhotite, freibergite et pyrite; 2) riches en Pb-Ag-Cu-Au et composées de galène, pyrite, freibergite et d’or et; 3) veines et remplacements riches en Ag-Pb-Zn et composées de sphalérite, galène, pyrite et freibergite. La datation Ar/Ar de séricite hydrothermale du gîte de Type ...

Atom distribution and interactions in Ag{sub x}Pt{sub 1-x} and Au{sub x}Pt{sub 1-x} surface alloys on Pt(111)

Energy Technology Data Exchange (ETDEWEB)

Roetter, Ralf T.; Bergbreiter, Andreas; Hoster, Harry E.; Behm, R. Juergen [Institute of Surface Chemistry and Catalysis, Ulm University, D-89069 Ulm (Germany)

2009-07-01

The atom distributions in Ag{sub x}Pt{sub 1-x}/Pt(111) and Au{sub x}Pt{sub 1-x}/Pt(111) surface alloys were studied by high resolution UHV-STM. These surfaces were prepared by submonolayer Ag (Au) metal deposition on Pt(111), followed by annealing at 900 K or 1000 K, respectively, which in both cases results in surface confined 2D alloys, with equilibrated distribution of the components. Both systems show a tendency towards two-dimensional clustering, which fits well to their known bulk immiscibility. Effective cluster interactions (ECIs) will be derived by a quantitative evaluation of the 2D atom distributions in the surface alloys. By comparing the ECIs for PtAg and PtAu on Pt(111), and considering that Ag and Au have almost similar lattice constants, the results allow conclusion on the physical origin of the tendency for clustering.

Neyshabour turquoise mine: the first Iron Oxide Cu-Au-U-LREE (IOCG mineralized system in Iran

Directory of Open Access Journals (Sweden)

Mohammad Hasan Karimpour

2011-11-01

Full Text Available Neyshabour turquoise mine is located in northwest of Neyshabour, southern Quchan volcanic belt. Eocene andesite and dacite forming as lava and pyroclastic rocks cover most of the area. Subvolcanic diorite to syenite porphyry (granitoids of magnetite series intruded the volcanic rocks. Both volcanic and subvolcanic rocks are highly altered. Four types of alteration are recognized including: silicification, argillic, calcification and propylitic. Silicification is dominant followed by argillic alteration. Mineralization is present as stockwork, disseminated and hydrothermal breccia. Hypogene minerals are pyrite, magnetite, specularite, chalcopyrite, and bornite. Secondary minerals are turquoise, chalcocite, covellite, and iron oxides. A broad zone of gossan has developed in the area. Oxidized zone has a thickness of about 80 m. Mineralized samples show high anomalies of Cu, Au, Zn, As, Mo, Co, U, LREE, Nb, and Th. Both aeromagnetic and radiometric (U and Th maps show very strong anomalies (10 × 5km within the mineralized area. Based on geology, alteration, mineralization, geochemistry, and geophysics, Neyshabour turquoise mine is a large Iron oxide Cu-Au-U-LREE (IOCG mineralized system. In comparison with other IOCG deposits, it has some similarities with Olympic Dam (Australia and Candelaria (Chile. In comparison with Qaleh Zari and Kuh Zar mines, Neyshabour turquoise mine is the first Iron oxide Cu-Au-U-LREE (IOCG mineralized system discovered in Iran.

Synthesis and crystal structure of the quaternary compound AgFe{sub 2}GaTe{sub 4}

Energy Technology Data Exchange (ETDEWEB)

Delgado, Gerzon E., E-mail: gerzon@ula.ve [Laboratorio de Cristalografía, Departamento de Química, Facultad de Ciencias, Universidad de Los Andes, Mérida 5101 (Venezuela, Bolivarian Republic of); Quintero, Eugenio; Tovar, Rafael; Grima-Gallardo, Pedro; Quintero, Miguel [Centro de Estudio de Semiconductores, Departamento de Física, Facultad de Ciencias, Universidad de Los Andes, Mérida 5101 (Venezuela, Bolivarian Republic of)

2014-11-15

Highlights: • New quaternary compound. • Synthesis from solid state reaction. • Crystal structure. • Rietveld refinement. - Abstract: The crystal structure of the quaternary compound AgFe{sub 2}GaTe{sub 4}, belonging to the system I–II{sub 2}–III–VI{sub 4}, was characterized by Rietveld refinement using X-ray powder diffraction data. The powder pattern was composed by 84.5% of the principal phase AgFe{sub 2}GaTe{sub 4} and 15.5% of the secondary phase FeTe. This material crystallizes with stannite structure in the tetragonal space group I-42m (N° 121), Z = 2, unit cell parameters a = 6.3409(2) Å, c = 12.0233(4) Å, V = 483.42(3) Å{sup 3}, and is isostructural with CuFe{sub 2}InSe{sub 4}.

Glass-like phonon scattering from a spontaneous nanostructure in AgSbTe2.

Science.gov (United States)

Ma, J; Delaire, O; May, A F; Carlton, C E; McGuire, M A; VanBebber, L H; Abernathy, D L; Ehlers, G; Hong, Tao; Huq, A; Tian, Wei; Keppens, V M; Shao-Horn, Y; Sales, B C

2013-06-01

Materials with very low thermal conductivity are of great interest for both thermoelectric and optical phase-change applications. Synthetic nanostructuring is most promising for suppressing thermal conductivity through phonon scattering, but challenges remain in producing bulk samples. In crystalline AgSbTe2 we show that a spontaneously forming nanostructure leads to a suppression of thermal conductivity to a glass-like level. Our mapping of the phonon mean free paths provides a novel bottom-up microscopic account of thermal conductivity and also reveals intrinsic anisotropies associated with the nanostructure. Ground-state degeneracy in AgSbTe2 leads to the natural formation of nanoscale domains with different orderings on the cation sublattice, and correlated atomic displacements, which efficiently scatter phonons. This mechanism is general and suggests a new avenue for the nanoscale engineering of materials to achieve low thermal conductivities for efficient thermoelectric converters and phase-change memory devices.

Heavy metals contamination and their risk assessment around the abandoned base metals and Au-Ag mines in Korea

Science.gov (United States)

Chon, Hyo-Taek

2017-04-01

Heavy metals contamination in the areas of abandoned Au-Ag and base metal mines in Korea was investigated in order to assess the level of metal pollution, and to draw general summaries about the fate of toxic heavy metals in different environments. Efforts have been made to compare the level of heavy metals, chemical forms, and plant uptake of heavy metals in each mine site. In the base-metals mine areas, significant levels of Cd, Cu, Pb and Zn were found in mine dump soils developed over mine waste materials and tailings. Leafy vegetables tend to accumulate heavy metals(in particular, Cd and Zn) higher than other crop plants, and high metal concentrations in rice crops may affect the local residents' health. In the Au-Ag mining areas, arsenic would be the most characteristic contaminant in the nearby environment. Arsenic and heavy metals were found to be mainly associated with sulfide gangue minerals, and the mobility of these metals would be enhanced by the effect of continuing weathering and oxidation. According to the sequential extraction of metals in soils, most heavy metals were identified as non-residual chemical forms, and those are very susceptible to the change of ambient conditions of a nearby environment. The concept of pollution index(PI) of soils gives important information on the extent and degree of multi-element contamination, and can be applied to the evaluation of mine soils before their agricultural use and remediation. The risk assessment process comprising exposure assessment, dose-response assessment, and risk characterization was discussed, and the results of non-cancer risk of As, Cd, and Zn, and those of cancer risk of As were suggested.

120 MeV Ag ion induced effects in Au/HfO2/Si MOSCAPs

Science.gov (United States)

Manikanthababu, N.; Prajna, K.; Pathak, A. P.; Rao, S. V. S. Nageswara

2018-05-01

HfO2/Si thinfilms were deposited by RF sputtering technique. 120 MeV Ag ion irradiation has been used to study the electrical properties of Au/HfO2/Si MOSCAPs. SHI (120 MeV Ag) induced annealing, defects creation and intermixing effects on the electrical properties of these systems have been studied. Here, we have observed that the high electronic excitation can cause a significant reduction of leakage currents in these MOSCAP devices. Various quantum mechanical tunneling phenomenon has been observed from the I-V characteristics.

Elastic, vibration and thermodynamic properties of Cu1‑x Ag x InTe2 (x = 0, 0.25, 0.5, 0.75 and 1) chalcopyrite compounds via first principles

Science.gov (United States)

Zhong, Yuhan; Wang, Peida; Mei, Huayue; Jia, Zhenyuan; Cheng, Nanpu

2018-06-01

CuInTe2 chalcopyrite compound is widely used in the fields of optoelectronics and pyroelectricity, and doping atoms can further improve the physical properties of the CuInTe2 compound. For all we know, this is the first time that the elastic behaviors and lattice dynamical properties of Ag-doped CuInTe2 compounds with the tetragonal system are determined theoretically. The elastic, lattice dynamical and thermal properties of Cu1‑x Ag x InTe2 (x = 0, 0.25, 0.5, 0.75 and 1) compounds have been investigated by using density functional theory. The obtained elastic constants of Cu1‑x Ag x InTe2 compounds indicate that these compounds are mechanically stable and elastic anisotropic. The anisotropy of the {001} plane is more obvious than those of the {100} and {010} planes. Additionally, with increasing Ag doping concentrations, the bulk and shear moduli of Cu1‑x Ag x InTe2 compounds decrease and their toughness improves. The phonon spectra and density of states reveal that Cu (or Ag) atoms in Cu1‑x Ag x InTe2 compounds form chemical bonds with Te atoms, and Cu-Te bonds are gradually replaced by Ag-Te bonds with increasing Ag doping concentration. Vibration modes of Cu1‑x Ag x InTe2 compounds at the {{Γ }} point in the Brillouin zone show that each Cu1‑x Ag x InTe2 (x = 0 and 1) crystal includes five irreducible representations (A1, A2, B1, B2 and E). As for Cu1‑x Ag x InTe2 (x = 0.25, 0.5 and 0.75) compounds, each crystal has three irreducible representations (A, B and E). The atomic displacements of several typical phonon modes in CuInTe2 crystals have been analyzed to deepen the understanding of lattice vibrations in Cu1‑x AgxInTe2 compounds. With increasing Ag doping concentration, the Debye temperatures of Cu1‑x Ag x InTe2 compounds decrease, while their heat capacities increase.

Study on the effect of nanoparticle bimetallic coreshell Au-Ag for sensitivity enhancement of biosensor based on surface plasmon resonance

International Nuclear Information System (INIS)

Widayanti; Abraha, K

2016-01-01

Bimetallic Au-Ag core-shell, a type of composite spherical nanoparticle consisting of a spherical Au core covered by Ag shell, have been used as active material for biomolecular analyte detection based on surface plasmon resonance (SPR) spectroscopy. SPR technology evolved into a key technology for characterization of biomolecular interaction. In this paper, we want to show the influence of nanoparticle bimettalic Au-Ag coreshell for optic respon of LSPR biosensor through attenuated total reflection (ATR) spectrum. The method consist of several steps begin from make a model LSPR system with Kretschmann configuration, dielectric function determination of composite bimetallic coreshell nanoparticle using effective medium theory approximation and the last is reflectivity calculation for size variation of core and shell bimetallic nanoparticle. Our result show that, by varying the radius of core and shell thickness, the peak of the reflectivity (ATR spectrum) shifted to the different angle of incident light and the addition of coreshell in SPR biosensor leads to enhancement the sensitivity. (paper)

Enzyme leaching of surficial geochemical samples for detecting hydromorphic trace-element anomalies associated with precious-metal mineralized bedrock buried beneath glacial overburden in northern Minnesota

Science.gov (United States)

Clark, Robert J.; Meier, A.L.; Riddle, G.; ,

1990-01-01

One objective of the International Falls and Roseau, Minnesota, CUSMAP projects was to develop a means of conducting regional-scale geochemical surveys in areas where bedrock is buried beneath complex glacially derived overburden. Partial analysis of B-horizon soils offered hope for detecting subtle hydromorphic trace-element dispersion patterns. An enzyme-based partial leach selectively removes metals from oxide coatings on the surfaces of soil materials without attacking their matrix. Most trace-element concentrations in the resulting solutions are in the part-per-trillion to low part-per-billion range, necessitating determinations by inductively coupled plasma/mass spectrometry. The resulting data show greater contrasts for many trace elements than with other techniques tested. Spatially, many trace metal anomalies are locally discontinuous, but anomalous trends within larger areas are apparent. In many instances, the source for an anomaly seems to be either basal till or bedrock. Ground water flow is probably the most important mechanism for transporting metals toward the surface, although ionic diffusion, electrochemical gradients, and capillary action may play a role in anomaly dispersal. Sample sites near the Rainy Lake-Seine River fault zone, a regional shear zone, often have anomalous concentrations of a variety of metals, commonly including Zn and/or one or more metals which substitute for Zn in sphalerite (Cd, Ge, Ga, and Sn). Shifts in background concentrations of Bi, Sb, and As show a trend across the area indicating a possible regional zoning of lode-Au mineralization. Soil anomalies of Ag, Co, and Tl parallel basement structures, suggesting areas that may have potential for Cobalt/Thunder Baytype silver viens. An area around Baudette, Minnesota, which is underlain by quartz-chlorite-carbonate-altered shear zones, is anomalous in Ag, As, Bi, Co, Mo, Te, Tl, and W. Anomalies of Ag, As, Bi, Te, and W tend to follow the fault zones, suggesting potential

Geology, mineralization, geochemistry and petrology of intrusions in the Kuh Zar Au-Cu deposit, Damghan

Directory of Open Access Journals (Sweden)

Payam Roohbakhsh

2018-04-01

secondary iron oxides such as goethite, hematite and limonite. Lithogeochemical exploration revealed Au (up to 598 ppb, Ag (up to 3747 ppb, Cu (up to 679 ppm, Pb (up to 1427 ppm and Zn (up to 1013 ppm anomalies. Based on geochemical studies, intrusive rocks have characteristics of high-K Calc-alkaline to slightly shoshonitic and they are within metaluminous to the slightly peraluminous range. Enrichment of LREE versus HREE, enrichment of LILE and depletion in HFSE indicate that the magma was formed in the subduction zones. The negative Eu anomaly is due to the presence of plagioclase as a residual mineral in the magma source. The parent magma is probably formed by the partial melting of amphibolites. The presence of monzonite porphyry source rock, QSP and propylitic alterations, pyrite disseminated mineralization and geochemical anomalies of Au and Cu in the Kuh Zar deposit represents Au-Cu porphyry mineralization in the area. Discussion Tectonic setting discrimination diagrams (Pearce et al., 1984 show that subvolcanic rocks plot almost on the fields of the volcanic arc granites (VAG. In the Rb/Zr vs. Nb diagram from (Brown et al., 1984, the samples are plotted in the field of primitive island arc/continental margin arc. The Torud-Chah Shirin Belt is a part of the Alborz magmatic assemblage (AMA. The AMA has been interpreted to represent the subduction of the Neo Tethyan oceanic lithosphere beneath the Central Iranian continental microplate and the subsequent continental collision of the Arabian and Iranian microplates in the late Cretaceous-early Cenozoic (Berberian and Berberian, 1981; Berberian et al., 1982; Alavi, 1994; Golonka, 2004. Acknowledgement This study has been supported by the Research Foundation of the Ferdowsi University of Mashhad, Iran (Project No. 27126.3. The authors would like to acknowledge the East Amethyst Laboratory for XRF analysis. We also thank the Gold Company of Iran for providing conditions for camping and accommodation. References Alavi, M

Magnetic, radiometric and gravity signatures of localities of epithermal gold deposits in Fiji

International Nuclear Information System (INIS)

Gunn, Peter J.; Mackey, Tim; Meixner, Tony J.

1998-01-01

Fiji contains several epithermal gold deposits and by studying the geophysical responses in the vicinity of these deposits it is possible to identify a set of geophysical characteristics which indicate localities where such deposits may be located. Epithermal gold deposits are formed above intrusive stocks resulting from subduction processes. The source intrusions for the deposits are normally covered by lavas and pyroclastic rocks and the irregular magnetic effects of these units obscure the magnetic effects of the intrusions. In Fiji however the source intrusions can be recognized as causing gravity highs and magnetic highs in upward continued magnetic data in which the magnetic effects of volcanic rocks are suppressed. Vents associated with the intrusions can be recognized as magnetic lows which sometimes contain a central high. Some vents and calderas can be recognized in digital elevation data. Increased potassium concentrations ca be interpreted to indicate potassium alteration associated with mineralizing processes. Fractures that may localize epithermal deposits can be recognized in the magnetic data and enhancements of the data such as produced by derivative operations. (author)

Les coûts du diabète sur 10 ans au Canada : intégration des coûts en soins de santé imputables au diabète à un modèle de prédiction de son incidence

Directory of Open Access Journals (Sweden)

Anja Bilandzic

2017-01-01

Full Text Available Introduction : Notre objectif était d’estimer les coûts de santé directs liés au traitement du diabète au Canada sur 10 ans, à l’aide de données de sondages nationaux et d’un outil de prévision du risque de diabète, ainsi que les coûts par personne. Méthodologie : Nous avons utilisé le Diabetes Population Risk Tool pour estimer le nombre de nouveaux cas de diabète chez les personnes âgées de 20 ans et plus sur 10 ans (jusqu'en 2022 à l’aide des données de 2011 et de 2012 de l’Enquête sur la santé dans les collectivités canadiennes. Nous avons évalué les coûts liés au diabète à partir d’une étude de cohorte faisant appel à l’appariement par score de propension, en utilisant la base de données sur le diabète de l’Ontario ainsi que d’autres données administratives. Nous avons calculé les coûts totaux en utilisant les coûts associés aux nouveaux cas, en tenant compte du sexe, de l’année du diagnostic et des taux de mortalité annuels dus à la maladie. Résultats : D'après nos calculs, le risque de développer le diabète sur 10 ans s’élevait pour la population canadienne en 2011-2012 à 9,98 %, soit 2,16 millions de nouveaux cas. Les coûts totaux en soins de santé imputables au diabète pendant cette période sont de 15,36 milliards (7,55 milliards pour les femmes et 7,81 milliards pour les hommes. Ce sont les hospitalisations de courte durée qui constituent la majeure partie de ces coûts (43,2 %. Des interventions menées au sein de la population entraînant une perte de poids de 5 % au sein de la population permettraient de réduire les coûts des soins de santé de 2,03 milliards de dollars. Une réduction du risque de 30 % obtenue grâce à des interventions auprès des personnes à plus haut risque de développer le diabète (c.-à-d. les 10 % au sommet du groupe à risque le plus élevé entraînerait des économies de l’ordrede 1,48 million de dollars. Conclusion : D'ici 2022

High-performance Ag0.8Pb18+xSbTe20 thermoelectric bulk materials fabricated by mechanical alloying and spark plasma sintering

International Nuclear Information System (INIS)

Wang Heng; Li Jingfeng; Nan Cewen; Zhou Min; Liu Weishu; Zhang Boping; Kita, Takuji

2006-01-01

Polycrystalline Ag n Pb m SbTe m+2n thermoelectric materials, whose compositions can be described as Ag 0.8 Pb 18+x SbTe 20 were prepared using a combined process of mechanical alloying and spark plasma sintering. Electric properties of the sintered samples with different Pb contents were measured from room temperature to 700 K. The maximum power factor of 1.766 mW/mK 2 was obtained at 673 K for the Ag 0.8 Pb 22 SbTe 20 sample, which corresponds to a high dimensionless figure of merit, ZT=1.37. This best composition is different from that reported before

Elemental Mass Balance of the Hydrothermal Alteration Associated with the Baturappe Epithermal Silver-Base Metal Prospect, South Sulawesi, Indonesia

OpenAIRE

Nur, Irzal; Idrus, Arifudin; Pramumijoyo, Subagyo; Harijoko, Agung; Watanabe, Koichiro; Imai, Akira; Jaya, Asri; Irfan, Ulva Ria; Sufriadin

2012-01-01

Abstract The Baturappe prospect situated in southernmost part of Sulawesi island, Indonesia, is a hydrothermal mineralization district which is characterized by occurrences of epithermal silver-base metal mineralizations. The mineralizations hosted in basaltic-andesitic volcanic rocks of the late Middle-Miocene Baturappe Volcanics. This paper discusses a recent study of relationships between alteration mineralogy and whole-rock geochemistry, which focused on elemental mass balance calculat...

Critical elements in Carlin, epithermal, and orogenic gold deposits

Science.gov (United States)

Goldfarb, Richard J.; Hofstra, Albert H.; Simmons, Stuart F.

2016-01-01

Carlin, epithermal, and orogenic gold deposits, today mined almost exclusively for their gold content, have similar suites of anomalous trace elements that reflect similar low-salinity ore fluids and thermal conditions of metal transport and deposition. Many of these trace elements are commonly referred to as critical or near-critical elements or metals and have been locally recovered, although typically in small amounts, by historic mining activities. These elements include As, Bi, Hg, In, Sb, Se, Te, Tl, and W. Most of these elements are now solely recovered as by-products from the milling of large-tonnage, base metal-rich ore deposits, such as porphyry and volcanogenic massive sulfide deposits.A combination of dominance of the world market by a single country for a single commodity and a growing demand for many of the critical to near-critical elements could lead to future recovery of such elements from select epithermal, orogenic, or Carlin-type gold deposits. Antimony continues to be recovered from some orogenic gold deposits and tellurium could potentially be a primary commodity from some such deposits. Tellurium and indium in sphalerite-rich ores have been recovered in the past and could be future commodities recovered from epithermal ores. Carlin-type gold deposits in Nevada are enriched in and may be a future source for As, Hg, Sb, and/or Tl. Some of the Devonian carbonaceous host rocks in the Carlin districts are sufficiently enriched in many trace elements, including Hg, Se, and V, such that they also could become resources. Thallium may be locally enriched to economic levels in Carlin-type deposits and it has been produced from Carlin-like deposits elsewhere in the world (e.g., Alsar, southern Macedonia; Lanmuchang, Guizhou province, China). Mercury continues to be recovered from shallow-level epithermal deposits, as well as a by-product of many Carlin-type deposits where refractory ore is roasted to oxidize carbon and pyrite, and mercury is then

Synthesis and characterization of the ternary telluroargentate K4[Ag18Te11

KAUST Repository

Davaasuren, Bambar; Dashjav, Enkhtsetseg; Rothenberger, Alexander

2014-01-01

The ternary potassium telluroargentate(I), K4[Ag18Te11], was prepared by solvothermal synthesis in ethylenediamine at 160 °C. It crystallizes in the cubic space group Fm3¯ m (no. 225) with the cell parameter a = 18.6589(6) Å. The crystal structure

Native gold from the Inagli Pt-Au placer deposit (the Aldan Shield, Russia): geochemical characteristics and implications for possible bedrock sources

Science.gov (United States)

Svetlitskaya, Tatyana V.; Nevolko, Peter A.; Kolpakov, Vladislav V.; Tolstykh, Nadezhda D.

2018-03-01

The Inagli alluvial Pt-Au placer deposit in the Republic of Sakha (Yakutia), Russia, is linked to the Inagli massif, one of the several Uralian-Alaskan-type alkaline-ultrabasic complexes in the Aldan Shield. Gold from the placer is heterogeneous in composition and is represented by three types. Type 1 gold is the most abundant and is characterized by simple Au-Ag alloys with 4-34 wt% Ag, low Cu (up to 0.08 wt%) and negligible Hg, Pt, and Pd contents, and silver-tellurium sulfosalts (Ag-Cu-Te-S-As compounds) in the inclusion suite. Silicate inclusions are biotite, K-feldspar, Fe-Mg amphibole, chlorite, plagioclase, Fe-Mg pyroxene, zircon, and titanite. Distinctive features of this gold type are most similar to those derived from low-sulfidation systems linked to iron oxide copper-gold or iron skarn types of mineralization. The bedrock source of type 1 gold could be related with monzonite to syenite intrusions surrounding the Inagli massif. Distinctive features of type 2 gold include a wide discontinuous range of Ag content (1-18 wt%), elevated Cu (up to 0.5 wt%), and occasional Pd (up to 0.3 wt%) levels, non-detectable Pt and Hg contents, and rare inclusions of simple sulfides (digenite, pyrrhotite) and Na amphibole. Type 3 gold is distinguished by a narrow range in Ag content (5-8 wt%), elevated Hg (0.5-1 wt%) contents, negligible Cu, Pt and Pd levels, and Au-Pb compounds + K-feldspar inclusions. Microchemical characteristics of type 2 and type 3 gold are interpreted as suggestive of an alkaline-magmatic-related fluid. Based on the grain morphology and microchemical signatures, potential bedrock sources for both gold types could be related to the numerous alkaline veins and potassic alteration zones within the dunite core. A comparison of the Inagli and the Kondyor placer gold allows to generate distinctive generic signatures for gold from Uralian-Alaskan-type alkaline-ultrabasic complexes in the Aldan Shield.

Infrared Spectroscopy and Raman Scattering Studies on the Structure of Ag2O. B2O3. TeO2 Glass

International Nuclear Information System (INIS)

Thazin Myint; Soe Soe Thin; Pho Kaung; Sein Htoon

2006-06-01

Infrared spectroscopy investigation of silver - borate - tellurite glasses in the system 0.4 Ag2 O. 0.6 (x B2 O2. (1-x) TeO2) for various of x (0 < x < 1) has been performed in order to understand the glass modifying properties of the TeO2. In pure crystalline TeO2 spectra observed absorption bands at 780 cm-1 and 660 cm-1 have been ascribed to the stretching vibration of TeO bonds in the TeO4 units. In the glass 0.4 Ag2 O. 0.6 (x B2 O3. (1-x) TeO2) the bands at 700 cm-1 and 694 cm-1 are assigned to the symmetric breathing vibration of the boroxol group and the pentaborate one. The glasses show bands at 630 cm-1 which corresponds to the vibrations due to TeO4 units

Electrical mobility of silver ion in Ag2O-B2O3-P2O5-TeO2 glasses.

Science.gov (United States)

Sklepić, Kristina; Vorokhta, Maryna; Mošner, Petr; Koudelka, Ladislav; Moguš-Milanković, Andrea

2014-10-16

The effect of adding TeO(2) into (100 - x)[0.5Ag(2)O - 0.1B(2)O(3) - 0.4P(2)O(5)] - xTeO(2), with 0-80 mol % TeO(2) glass, on the structural changes and electrical properties has been investigated. DSC and thermodilatomery were used to study their thermal behavior, structure was studied by Raman spectroscopy, and electrical properties have been studied by impedance spectroscopy over a wide temperature and frequency range. The introduction of TeO(2) as a third glass former to the glass network causes the structural transformation from TeO(3) (tp) to TeO(4) (tbp) which contributes to the changes in conductivity. The glasses with low TeO(2) content show only a slow decrease in dc conductivity with addition of TeO(2) due to the increase of the number of nonbridging oxygens, which increases the mobility of Ag(+) ions. The steep decrease in conductivity for glasses containing more than 40 mol % TeO(2) is a result of decrease of the Ag(2)O content and stronger cross-linkage in glass network through the formation of more Te-(eq)O(ax)-Te bonds in TeO(4) tbp units. The glasses obey ac conductivity scaling with respect to temperature, implying that the dynamic process is not temperature dependent. On the other hand, the scaling of the spectra for different glass compositions showed the deviations from the Summerfield scaling because of the local structural disorder which occurs as a result of the structural modifications in the tellurite glass network.

A colorimetric nitrite detection system with excellent selectivity and high sensitivity based on Ag@Au nanoparticles.

Science.gov (United States)

Li, Tianhua; Li, Yonglong; Zhang, Yujie; Dong, Chen; Shen, Zheyu; Wu, Aiguo

2015-02-21

Excessive uptake of NO2(-) is detrimental to human health, but the currently available methods used to sensitively detect this ion in the environment are cumbersome and expensive. In this study, we developed an improved NO2(-) detection system based on a redox etching strategy of CTAB-stabilized Ag-Au core-shell nanoparticles (Ag@AuNPs). The detection mechanism was verified by UV-Vis spectroscopy, TEM and XPS. The detection system produces a color change from purple to colorless in response to an increase of NO2(-) concentration. The selectivity of detection of NO2(-), both with the unaided eye and by measurement of UV-Vis spectra, is excellent in relation to other ions, including Cu(2+), Co(2+), Ni(2+), Cr(3+), Al(3+), Pb(2+), Cd(2+), Ca(2+), Ba(2+), Zn(2+), Mn(2+), Mg(2+), Fe(3+), Hg(2+), Ag(+), K(+), F(-), PO4(3-), C2O4(2-), SO3(2-), CO3(2-), SO4(2-), NO3(-) and CH3-COO(-) (Ac(-)). The limit of detection (LOD) for NO2(-) is 1.0 μM by eye and 0.1 μM by UV-Vis spectroscopy. The LOD by eye is lower than the lowest previously reported value (4.0 μM). There is a good linear relationship between A/A0 and the concentration of NO2(-) from 1.0 to 20.0 μM NO2(-), which permits a quantitative assay. The applicability of our detection system was also verified by analysis of NO2(-) in tap water and lake water. The results demonstrate that our Ag@AuNP-based detection system can be used for the rapid colorimetric detection of NO2(-) in complex environmental samples, with excellent selectivity and high sensitivity.

Bottom-up processing of thermoelectric nanocomposites from colloidal nanocrystal building blocks: the case of Ag2Te–PbTe

International Nuclear Information System (INIS)

Cadavid, Doris; Ibáñez, Maria; Gorsse, Stéphane; López, Antonio M.; Cirera, Albert; Morante, Joan Ramon; Cabot, Andreu

2012-01-01

Nanocomposites are highly promising materials to enhance the efficiency of current thermoelectric devices. A straightforward and at the same time highly versatile and controllable approach to produce nanocomposites is the assembly of solution-processed nanocrystal building blocks. The convenience of this bottom-up approach to produce nanocomposites with homogeneous phase distributions and adjustable composition is demonstrated here by blending Ag 2 Te and PbTe colloidal nanocrystals to form Ag 2 Te–PbTe bulk nanocomposites. The thermoelectric properties of these nanocomposites are analyzed in the temperature range from 300 to 700 K. The evolution of their electrical conductivity and Seebeck coefficient is discussed in terms of the blend composition and the characteristics of the constituent materials.

Determination of silver, gold, zinc and copper in mineral samples by various techniques of instrumental neutron activation analysis

International Nuclear Information System (INIS)

Rodriguez R, N. I.; Rios M, C.; Pinedo V, J. L.; Yoho, M.; Landsberger, S.

2015-09-01

Using the method of instrumental neutron activation analysis, mineral exploration samples were analyzed in order to determine the concentrations of silver, gold, zinc and copper; these minerals being the main products of benefit of Tizapa and Cozamin mines. Samples were subjected to various techniques, where the type of radiation and counting methods were chosen based on the specific isotopic characteristics of each element. For calibration and determination of concentrations the comparator method was used, certified standards were subjected to the same conditions of irradiation and measurement that the prospecting samples. The irradiations were performed at the research reactor TRIGA Mark II of the University of Texas at Austin. The silver concentrations were determined by Cyclical Epithermal Neutron Activation Analysis. This method in combination with the transfer pneumatic system allowed a good analytical precision and accuracy in prospecting for silver, from photo peak measurement 657.7 keV of short half-life radionuclide 110 Ag. For the determination of gold and zinc, Epithermal Neutron Activation Analysis was used, the photo peaks analyzed corresponded to the energies 411.8 keV of radionuclide 199 Au and 438.6 keV of metastable radionuclide 69m Zn. On the other hand, copper quantification was based on the photo peak analysis of 1039.2 keV produced by the short half-life radionuclide 66 Cu, by Thermal Neutron Activation Analysis. The photo peaks measurement corresponding to gold, zinc and copper was performed using a Compton suppression system, which allowed an improvement in the signal to noise relationship, so that better detection limits and low uncertainties associated with the results were obtained. Comparing elemental concentrations the highest values in silver, zinc and copper was for samples of mine Tizapa. Regarding gold values were found in the same range for both mines. To evaluate the precision and accuracy of the methods used, various geological

Effect of Refractive Index of Substrate on Fabrication and Optical Properties of Hybrid Au-Ag Triangular Nanoparticle Arrays

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Jing Liu

2015-05-01

Full Text Available In this study, the nanosphere lithography (NSL method was used to fabricate hybrid Au-Ag triangular periodic nanoparticle arrays. The Au-Ag triangular periodic arrays were grown on different substrates, and the effect of the refractive index of substrates on fabrication and optical properties was systematically investigated. At first, the optical spectrum was simulated by the discrete dipole approximation (DDA numerical method as a function of refractive indexes of substrates and mediums. Simulation results showed that as the substrates had the refractive indexes of 1.43 (quartz and 1.68 (SF5 glass, the nanoparticle arrays would have better refractive index sensitivity (RIS and figure of merit (FOM. Simulation results also showed that the peak wavelength of the extinction spectra had a red shift when the medium’s refractive index n increased. The experimental results also demonstrated that when refractive indexes of substrates were 1.43 and 1.68, the nanoparticle arrays and substrate had better adhesive ability. Meanwhile, we found the nanoparticles formed a large-scale monolayer array with the hexagonally close-packed structure. Finally, the hybrid Au-Ag triangular nanoparticle arrays were fabricated on quartz and SF5 glass substrates and their experiment extinction spectra were compared with the simulated results.

Nanostructured KTaTeO6 and Ag-doped KTaTeO6 Defect Pyrochlores: Promising Photocatalysts for Dye Degradation and Water Splitting

Science.gov (United States)

Venkataswamy, Perala; Sudhakar Reddy, CH.; Gundeboina, Ravi; Sadanandam, Gullapelli; Veldurthi, Naveen Kumar; Vithal, M.

2018-03-01

In this study, the nanostructured parent KTaTeO6 (KTTO) and Ag-doped KTaTeO6 (ATTO) catalysts with defect pyrochlore structure were prepared by solid-state and ion-exchange methods, respectively. The synthesized materials were characterized by various techniques to determine their chemical composition, morphology and microstructural features. The XRD studies show that both KTTO and ATTO have cubic structure (space group Fd3m) with high crystallinity. The doping of Ag altered the BET surface area of parent KTTO. The nano nature of the samples was studied by TEM images. A considerable red-shift in the absorption edge is observed for ATTO compared to KTTO. Incorporation of Ag+ in the KTTO lattice is clearly identified from EDX, elemental mapping and XPS results. Degradation of methyl violet and solar water splitting reactions were used to access the photocatalytic activity of KTTO and ATTO. The results obtained suggest that compared to KTTO, the ATTO showed higher photocatalytic activity in both cases. The favourable properties such as high surface area, more surface hydroxyl groups, stronger light absorption in visible region and narrower band gap energy were supposed to be the reasons for the high activity observed in ATTO.

Temperature dependence of thermal properties of Ag8In14Sb55Te23 phase-change memory materials

International Nuclear Information System (INIS)

Jiao, Xinbing; Gan, Fuxi; Wei, Jingsong; Xiao, Mufei

2009-01-01

The dependence of thermal properties of Ag 8 In 14 Sb 55 Te 23 phase-change memory materials in crystalline and amorphous states on temperature was measured and analyzed. The results show that in the crystalline state, the thermal properties monotonically decrease with the temperature and present obvious crystalline semiconductor characteristics. The heat capacity, thermal diffusivity, and thermal conductivity decrease from 0.35 J/gK, 1.85 mm 2 /s, and 4.0 W/mK at 300 K to 0.025 J/gK, 1.475 mm 2 /s, and 0.25 W/mK at 600 K, respectively. In the amorphous state, while the dependence of thermal properties on temperature does not present significant changes, the materials retain the glass-like thermal characteristics. Within the temperature range from 320 K to 440 K, the heat capacity fluctuates between 0.27 J/gK and 0.075 J/gK, the thermal diffusivity basically maintains at 0.525 mm 2 /s, and the thermal conductivity decreases from 1.02 W/mK at 320 K to 0.2 W/mK at 440 K. Whether in the crystalline or amorphous state, Ag 8 In 14 Sb 55 Te 23 are more thermally active than Ge 2 Sb 2 Te 5 , that is, the Ag 8 In 14 Sb 55 Te 23 composites bear stronger thermal conduction and diffusion than the Ge 2 Sb 2 Te 5 phase-change memory materials. (orig.)

Remote Sensing for Mineral Exploration in Central Portugal

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Ricardo Manuel

2017-09-01

Full Text Available Central Portugal is well known for the existence of Sn-W and Au-Ag mineral occurrences primarily associated with hydrothermal processes. Despite the economic and strategic importance of such occurrences, the detailed geology of this particular region is poorly known and there is an obvious absence of geological mapping at an adequate scale. Remote sensing techniques were used in order to increase current geological knowledge of the Góis–Castanheira de Pêra area (600 km2 and to guide future exploration stages by targeting and prioritising potential locations. Digital image processing algorithms, such as Red, Green, Blue (RGB colour composites, digital spatial filters, band ratios and Principal Components Analysis, were applied to Landsat 8 imagery and elevation data. Lineaments were extracted relying on geological photointerpretation criteria, allowing the identification of new geological–structural elements. Fieldwork was carried out in order to validate the remote sensing interpretations. Integration of remote sensing data with other information sources led to the definition of locations possibly suitable for hosting Sn-W and Au-Ag mineral occurrences. These areas were ranked according to their mineral potential. Targeting the most promising locations resulted in a reduction to less than 10% of the original study area (50.5 km2.

N-Heterocyclic carbenes on close-packed coinage metal surfaces: bis-carbene metal adatom bonding scheme of monolayer films on Au, Ag and Cu.

Science.gov (United States)

Jiang, Li; Zhang, Bodong; Médard, Guillaume; Seitsonen, Ari Paavo; Haag, Felix; Allegretti, Francesco; Reichert, Joachim; Kuster, Bernhard; Barth, Johannes V; Papageorgiou, Anthoula C

2017-12-01

By means of scanning tunnelling microscopy (STM), complementary density functional theory (DFT) and X-ray photoelectron spectroscopy (XPS) we investigate the binding and self-assembly of a saturated molecular layer of model N -heterocyclic carbene (NHC) on Cu(111), Ag(111) and Au(111) surfaces under ultra-high vacuum (UHV) conditions. XPS reveals that at room temperature, coverages up to a monolayer exist, with the molecules engaged in metal carbene bonds. On all three surfaces, we resolve similar arrangements, which can be interpreted only in terms of mononuclear M(NHC) 2 (M = Cu, Ag, Au) complexes, reminiscent of the paired bonding of thiols to surface gold adatoms. Theoretical investigations for the case of Au unravel the charge distribution of a Au(111) surface covered by Au(NHC) 2 and reveal that this is the energetically preferential adsorption configuration.

Interdiffusion in epitaxial, single-crystalline Au/Ag thin films studied by Auger electron spectroscopy sputter-depth profiling and positron annihilation

International Nuclear Information System (INIS)

Noah, Martin A.; Flötotto, David; Wang, Zumin; Reiner, Markus; Hugenschmidt, Christoph; Mittemeijer, Eric J.

2016-01-01

Interdiffusion in epitaxial, single-crystalline Au/Ag bilayered thin films on Si (001) substrates was investigated by Auger electron spectroscopy (AES) sputter-depth profiling and by in-situ positron annihilation Doppler broadening spectroscopy (DBS). By the combination of these techniques identification of the role of vacancy sources and sinks on interdiffusion in the Au/Ag films was possible. It was found that with precise knowledge of the concentration-dependent self-diffusion and impurity diffusion coefficients a distinction between the Darken-Manning treatment and Nernst-Planck treatment can be made, which is not possible on the basis of the determined concentration-depth profiles alone.

anti p and anti Λ production in Si+Au collisions at the AGS

International Nuclear Information System (INIS)

Wu, Yuedong

1996-01-01

Anti p and anti Λ production in central Si + Au collisions has been measured by E589 at the BNL-AGS. Preliminary m perpendicular spectra are presented for anti p's and anti Λ's. The dn/dy distribution for anti p's is also presented. Based on the anti p and anti Λ measurements, anti Λ/anti p ratios are calculated in the rapidity range of 1.1-1.5

Femtosecond Laser Fabricated Ag@Au and Cu@Au Alloy Nanoparticles for Surface Enhanced Raman Spectroscopy Based Trace Explosives Detection

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Moram Sree Satya Bharati

2018-03-01

Full Text Available Herein we present results from our detailed studies on the fabrication of Ag@Au and Cu@Au alloy nanoparticles (NPs using the femtosecond laser ablation in liquid technique. The NPs were obtained by ablating the pure Ag, Cu targets (bulk in HAuCl4 (5 mM solution. The absorption properties of the obtained NPs colloids were characterized using UV-Visible absorption spectrometer and their size, shape, and crystallinity were investigated using the XRD, FESEM and TEM techniques. The fabricated NPs were utilized for sensing of explosive molecules such as 2,4,6-trinitrophenol (PA, 2,4-dinitrotoluene (DNT and a common dye methylene blue (MB using the surface enhanced Raman spectroscopy (SERS technique. The detection limit in terms of weight was as low as few nano-grams in the case of nitroaromatic explosive compounds (PA, DNT and few picograms in the case of a common dye molecule (MB. Typical enhancement factors achieved were estimated to be ~104, ~105, and ~107, respectively, for PA, DNT, and MB. The significance of the present work lies in exploring the performance of the prepared NPs being used as SERS substrates for explosives detection using a portable Raman instrument. Such capability enables one to carry the spectrometer to the point of interest in the field and evaluate any hazardous samples within a short period of time.

Bimetallic Ag-Pt and Au-Pt aggregates synthesized by radiolysis

International Nuclear Information System (INIS)

Remita, S.; Mostafavi, M.; Delcourt, M.O.

1996-01-01

Irradiating aqueous solutions containing both Ag 2 So 4 and K 2 PtCl 4 leads to intermetallic aggregates of various sizes according to the stabilizing agent: polyvinylalcohol, polyacrylic acid or polyacrylate. In the last case, the particle diameter is 1.5 nm. The bimetallic character is evidenced in all cases by the spectral changes of such sols compared to pure silver sols which display a characteristic surface plasmon absorption band. This plasmon band disappears when 10 to 20 at.% or more Pr is present. Observation by TEM gives an estimation of the particle sizes. Comparable results have been obtained for Au-Pt particles. (author)

Bimetallic Ag-Pt and Au-Pt aggregates synthesized by radiolysis

Energy Technology Data Exchange (ETDEWEB)

Remita, S; Mostafavi, M; Delcourt, M O [Paris-11 Univ., 91 - Orsay (France)

1996-02-01

Irradiating aqueous solutions containing both Ag{sub 2}So{sub 4} and K{sub 2}PtCl{sub 4} leads to intermetallic aggregates of various sizes according to the stabilizing agent: polyvinylalcohol, polyacrylic acid or polyacrylate. In the last case, the particle diameter is 1.5 nm. The bimetallic character is evidenced in all cases by the spectral changes of such sols compared to pure silver sols which display a characteristic surface plasmon absorption band. This plasmon band disappears when 10 to 20 at.% or more Pr is present. Observation by TEM gives an estimation of the particle sizes. Comparable results have been obtained for Au-Pt particles. (author).

Natural nanostructure and superlattice nanodomains in AgSbTe{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Carlton, Christopher E.; De Armas, Ricardo; Shao-Horn, Yang, E-mail: delaireoa@ornl.gov, E-mail: shaohorn@mit.edu [Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139 (United States); Ma, Jie [Quantum Condensed Matter Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831 (United States); May, Andrew F.; Delaire, Olivier, E-mail: delaireoa@ornl.gov, E-mail: shaohorn@mit.edu [Materials Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831 (United States)

2014-04-14

AgSbTe{sub 2} has long been of interest for thermoelectric applications because of its favorable electronic properties and its low lattice thermal conductivity of ∼0.7 W/mK. In this work, we report new findings from a high-resolution transmission electron microscopy study revealing two nanostructures in single crystal Ag{sub 1−x}Sb{sub 1+x}Sb{sub 2+x} (with x = 0, 0.1, 0.2); (i) a rippled natural nanostructure with a period of ∼2.5–5 nm and (ii) superlattice ordered nanodomains consistent with cation ordering predicted in previous density functional theory studies. These nanostructures, combined with point-defects, probably serve as sources of scattering for phonons, thereby yielding a low lattice thermal conductivity over a wide temperature range.

Nanocrystals of the quaternary thermoelectric materials: AgPb{sub m}SbTe{sub m+2}(m=1-18): Phase-segregated or solid solutions?

Energy Technology Data Exchange (ETDEWEB)

Arachchige, Indika U [Department of Chemistry, Northwestern University Evanston, IL (United States); Wu, Jinsong; Dravid, Vinayak P [Department of Materials Science and Engineering, Northwestern University Evanston, IL (United States); Kanatzidis, Mercouri G [Department of Chemistry, Northwestern University Evanston, IL (United States); Material Science Division, Argonne National Laboratory Argonne, IL (United States)

2008-10-02

Facile synthesis of a series of thermoelectrically relevant AgPb{sub m}SbTe{sub m+2}(m=1-18) nanoparticles is carried out by using a colloidal synthetic route. As-synthesized nanocrystals are spherical in geometry and adopt a cubic NaCl-type structure. These quaternary nanocrystals behave as solid solutions at room temperature and tend to phase separate into AgSbTe{sub 2} and PbTe upon annealing at moderately high temperature. (Abstract Copyright [2008], Wiley Periodicals, Inc.)

Digestive ripening facilitated atomic diffusion at nanosize regime: Case of AuIn{sub 2} and Ag{sub 3}In intermetallic nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Arora, Neha [Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bangalore 560 012 (India); Jagirdar, Balaji R., E-mail: jagirdar@ipc.iisc.ernet.in [Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bangalore 560 012 (India); Klabunde, Kenneth J. [Department of Chemistry, Kansas State University, Manhattan, KS 66506 (United States)

2014-10-15

Highlights: • A digestive ripening facilitated interatomic diffusion process is presented. • Nearly monodisperse AuIn{sub 2} and Ag{sub 3}In intermetallic nanoparticles were synthesized. • Optimization of reaction temperature facilitates interatomic transfer. • Presence of excess ligand plays a crucial role in the digestive ripening process. - Abstract: Monodisperse colloidal gold–indium (AuIn{sub 2}) intermetallic nanoparticles have been synthesized from Au and In colloids using the digestive ripening process. Formation of the intermetallic proceeds via digestive ripening facilitated atomic diffusion of Au and In atoms from the Au and In nanoparticles followed simultaneously by their growth in the solution. Optimization of the reaction temperature was found to be crucial for the formation of AuIn{sub 2} intermetallic from gold and indium nanoparticles. Transmission electron microscopy revealed the presence of nearly monodisperse nanoparticles of Au and AuIn{sub 2} with particle size distribution of 3.7 ± 1.0 nm and 5.0 ± 1.6 nm, respectively. UV–visible spectral studies brought out the absence of SPR band in pure AuIn{sub 2} intermetallic nanoparticles. Optical study and electron microscopy, in combination with powder X-ray diffraction established phase pure AuIn{sub 2} intermetallic nanoparticles unambiguously. The potential of such an unprecedented approach has been further exploited in the synthesis of Ag{sub 3}In intermetallic nanoparticles with the dimension of less than 10 nm.

Simple synthesis of ultra-long Ag2Te nanowires through solvothermal co-reduction method

International Nuclear Information System (INIS)

Xiao Feng; Chen Gang; Wang Qun; Wang Lin; Pei Jian; Zhou Nan

2010-01-01

Ultra-long single crystal β-Ag 2 Te nanowires with the diameter of about 300 nm were fabricated through a solvothermal route in ethylene glycol (EG) system without any template. The long single crystal wires were curves, with high purity, well-crystallized, and dislocation-free and characterized by using X-ray powder diffraction (XRD), Differential scanning calorimetry (DSC) analysis, X-ray photoelectron spectroscope (XPS), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM) and high-resolution transmission microscopy (HRTEM). The detailed topotactic transformation process from particles into single crystal wires was studied. Furthermore, the electrical conductivity and Seebeck coefficient have been systematically studied between 300 and 600 K. - Graphical abstract: Ultra-long single crystal β-Ag 2 Te nanowires with the diameter of about 300 nm were fabricated by the solvothermal route in ethylene glycol (EG) system without any template. The diagram displays the variation of the phases and morphologies of products with different reaction time.

Intriguing centrality dependence of the Au-Au source size at the AGS

International Nuclear Information System (INIS)

Baker, M.D.

1996-01-01

One of the main goals of high energy heavy ion physics is to establish the existence of a deconfined phase of nuclear matter--the quark-gluon plasma--at high temperatures or densities. One possible signature of such a phase transition, especially if it were first order, would be a larger source size or lifetime than a similar hadronic system. At current AGS energies, we attempt to form a quark- gluon plasma by achieving a high baryon density for a period of time in the center of the collision region. For a given density threshold, the size of this high density region should be a strong function of the impact parameter: the more central the event, the larger the high density region. Therefore, one possible signature of a quark-gluon plasma would be a sudden change in system lifetime or size as a function of the centrality of the collision. In this talk we present an intriguing effect which was not predicted for simple hadronic systems: a rapid increase of the HBT-measured source radius parameter for pion pairs with increasing centrality for Au-Au collisions at a beam momentum of 11.45 A GeV/c on a fixed target. Experience has shown, however, that we must be cautious in our interpretation. A complete understanding of the collision dynamics at a given energy must be built up from several measurements and new, but conventional, hadronic explanations must be considered for such unexpected effects. More study is needed, therefore, before any strong conclusions can be reached

Evaluation of colloidal Ag and Ag-alloys as anode electrocatalysts for direct borohydride fuel cells

Energy Technology Data Exchange (ETDEWEB)

Atwan, Mohammed H.; Northwood, Derek O. [Mechanical, Auto, and Materials Engineering, University of Windsor, Windsor, N9B 3P4 (Canada); Gyenge, Elod L. [Chemical and Biological Engineering, The University of British Colombia, Vancouver, BC, V6T 1Z4 (Canada)

2007-10-15

In this study, colloidal silver and silver-alloys (Ag-Pt, Ag-Au, Ag-Ir, and Ag-Pd) prepared by the Boenneman technique were evaluated as anode catalysts for sodium borohydride oxidation using cyclic voltammetry (CV), chronoamperometry (CA), chronopotentiometry (CP) and rotating disk electrode (RDE) voltammetry. The CV results show that the colloidal Ag-alloys were electrochemically active towards borohydride oxidation with oxidation potentials ranging between -0.7 and 0.4 V vs. Hg/HgO (MOE). The most negative oxidation potential was recorded on Ag-Pt. CA results show that the steady state current density was highest on Ag-Pt, followed by Ag-Ir, Ag-Au, and Ag-Pd. The lowest overpotential was recorded on Ag-Ir for a current step change of 10mAcm{sup -2}. A significant temperature effect and a small rotation speed effect were found in the rotating disc voltammetry for all the investigated colloids. The highest peak current was recorded on Ag-Au, while the most negative peak potential was recorded on Ag-Ir. (author)

High stability of the goldalloy fullerenes: A density functional theory investigation of M12@Au20 (M = Na, Al, Ag, Sc, Y, La, Lu, and Au) clusters

International Nuclear Information System (INIS)

Zhang Meng; Feng Xiao-Juan; Zhao Li-Xia; Zhang Hong-Yu; Luo You-Hua

2012-01-01

Discovering highly stable metal fullerenes such as the celebrated C 60 is interesting in cluster science as they have potential applications as building blocks in new nanostructures. We here investigated the structural and electronic properties of the fullerenes M 12 @Au 20 (M = Na, Al, Ag, Sc, Y, La, Lu, and Au), using a first-principles investigation with the density functional theory. It is found that these compound clusters possess a similar cage structure to the icosahedral Au 32 fullerene. La 12 @Au 20 is found to be particularly stable among these clusters. The binding energy of La 12 @Au 20 is 3.43 eV per atom, 1.05 eV larger than that in Au 32 . The highest occupied molecular orbital-lowest unoccupied molecular orbital (HOMO-LUMO) gap of La 12 @Au 20 is only 0.31 eV, suggesting that it should be relatively chemically reactive. (condensed matter: structural, mechanical, and thermal properties)

Some Key Features and Possible Origin of the Metamorphic Rock-Hosted Gold Mineralization in Buru Island, Indonesia

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Arifudin Idrus

2014-07-01

Full Text Available DOI: 10.17014/ijog.v1i1.172This paper discusses characteristics of some key features of the primary Buru gold deposit as a tool for a better understanding of the deposit genesis. Currently, about 105,000 artisanal and small-scale gold miners (ASGM are operating in two main localities, i.e. Gogorea and Gunung Botak by digging pits/shafts following gold-bearing quartz vein orientation. The gold extraction uses mercury (amalgamation and cyanide processing. The field study identifies two types/generations of quartz veins namely (1 Early quartz veins which are segmented, sigmoidal, dis­continous, and parallel to the foliation of host rock. The quartz vein is lack of sulfides, weak mineralized, crystalline, relatively clear, and maybe poor in gold, and (2 Quartz veins occurred within a ‘mineralized zone’ of about 100 m in width and ~1,000 m in length. The gold mineralization is strongly overprinted by an argillic alteration zone. The mineralization-alteration zone is probably parallel to the mica schist foliation and strongly controlled by N-S or NE-SW-trending structures. The gold-bearing quartz veins are characterized by banded texture particularly colloform following host rock foliation and sulphide banding, brecciated, and rare bladed-like texture. The alteration types consist of propylitic (chlorite, calcite, sericite, argillic, and carbonation represented by graphite banding and carbon flakes. The ore mineralization is characterized by pyrite, native gold, pyrrhotite, and arsenopyrite. Cinnabar, stibnite, chalcopyrite, galena, and sphalerite are rare or maybe absent. In general, sulphide minerals are rare (<3%. Fifteen rock samples were collected in Wamsaid area for geochemical assaying for Au, Ag, As, Sb, Hg, Cu, Pb, and Zn. Eleven of fifteen samples yielded more than 1.00 g/t Au, in which six of them are in excess of 3.00 g/t Au. It can be noted that all high-grade samples are originally or containing limonitic materials, that suggest

Hydrothermal Evolution of the Giant Cenozoic Kadjaran porphyry Cu-Mo deposit, Tethyan metallogenic belt, Armenia, Lesser Caucasus: mineral paragenetic, cathodoluminescence and fluid inclusion constraints

Science.gov (United States)

Hovakimyan, Samvel; Moritz, Robert; Tayan, Rodrik; Rezeau, Hervé

2016-04-01

The Lesser Caucasus belongs to the Central segment of the Tethyan metallogenic belt and it is a key area to understand the metallogenic evolution between the Western & Central parts of the Tethyan belt and its extension into Iran. Zangezur is the most important mineral district in the southernmost Lesser Caucasus. It is a component of the South Armenian block, and it was generated during the convergence and collision of the southern margin of the Eurasian plate and the northern margin of the Arabian plate, and terranes of Gondwana origin (Moritz et al., in press). The Zangezur ore district consists of the Tertiary Meghri-Ordubad composite pluton, which is characterized by a long-lasting Eocene to Pliocene magmatic, tectonic and metallogenic evolution. It hosts major porphyries Cu-Mo and epithermal Au - polymetallic deposits and occurrences, including the giant world class Kadjaran porphyry Cu-Mo deposit (2244 Mt reserves, 0.3% Cu, 0.05% Mo and 0.02 g/t Au). The Kadjaran deposit is hosted by a monzonite intrusion (31.83±0.02Ma; Moritz et al., in press). Detailed field studies of the porphyry stockwork and veins of the different mineralization stages, their crosscutting and displacement relationships and the age relationship between different paragenetic mineral associations were the criteria for distinction of the main stages of porphyry mineralization at the Kadjaran deposit. The economic stages being: quartz- molybdenite, quartz-molybdenite-chalcopyrite, and quartz-chalcopyrite. The main paragenetic association of the Kadjaran porphyry deposit includes pyrite, molybdenite, chalcopyrite, bornite, chalcocite, pyrrhotite, covellite, sphalerite, and galena. Recent field observations in the Kadjaran open pit revealed the presence of epithermal veins with late vuggy silica and advanced argillic alteration in the north-eastern and eastern parts of the deposit. They are distributed as separate veins and have also been recognized in re-opened porphyry veins and in

Granite-related hypothermal uranium mineralization in South China

International Nuclear Information System (INIS)

Liu, X.; Wu, J.; Pan, J.; Zhu, M.

2014-01-01

As one of the important geological types, granite-related uranium deposits account for about 29% of the total discovered natural uranium resources in China. Most of the granite-related uranium deposits located in Taoshan - Zhuguang uranium metallogenic belt, South China. In addition to the typical pitchblende vein-type uranium mineralization of epithermal metallogenic system, a new type of granite-related uranium mineralization with characteristics of hypothermal matallogenic system was discovered in South China by current studies. However, hypothermal is contact thermal to epithermal mineralization, and not the conventional intrusive high temperature mineralization. Hypothermal uranium mineralization is presented by disseminated uraninite or pitchblende stockwork in fissures in granites normally with extensive alkaline alteration. The high temperature mineral assemblage of uraninite associate with scheelite and tourmaline was identified in hypothermal uranium mineralization. Fluid inclusion studies on this type mineralization indicated the middle to high temperature (>250℃) mineralization with the mixing evidence of ore forming solution derived from deep level, and the boiling and mixing of ore forming solution are regarded as the dominant mineralization mechanism for the precipitating of uranium. In contrast to the mineralization ages of 67 Ma to 87 Ma for typical pitchblende vein mineralization of epithermal metallogenic system, the mineralization age is older than 100 Ma for hypothermal uranium mineralization in granite. In the Shituling deposit, Xiazhuang uranium ore field, uraninite and pitchblende micro veins with extensive potassic alteration, chloritization and sericitization are hosted in fissures of Indo-Chinese epoch granites with the uranium mineralization age of 130 Ma to 138 Ma with a mineralization temperature of 290℃ to 330℃ indicated. Other examples sharing the similar characters of hypothermal uranium mineralization have been recognized in

Critical Factors Controlling Pd and Pt Potential in Porphyry Cu–Au Deposits: Evidence from the Balkan Peninsula

Directory of Open Access Journals (Sweden)

Demetrios G. Eliopoulos

2014-03-01

Full Text Available Porphyry Cu–Au–Pd±Pt deposits are significant Au resources, but their Pd and Pt potential is still unknown. Elevated Pd, Pt (hundreds of ppb and Au contents are associated with typical stockwork magnetite-bornite-chalcopyrite assemblages, at the central parts of certain porphyry deposits. Unexpected high grade Cu–(Pd+Pt (up to 6 ppm mineralization with high Pd/Pt ratios at the Elatsite porphyry deposit, which is found in a spatial association with the Chelopech epithermal deposit (Bulgaria and the Skouries porphyry deposit, may have formed during late stages of an evolved hydrothermal system. Estimated Pd, Pt and Au potential for porphyry deposits is consistent with literature model calculations demonstrating the capacity of aqueous vapor and brine to scavenge sufficient quantities of Pt and Pd, and could contribute to the global platinum-group element (PGE production. Critical requirements controlling potential of porphyry deposits may be from the metals contained in magma (metasomatized asthenospheric mantle wedge as indicated by significant Cr, Co, Ni and Re contents. The Cr content may be an indicator for the mantle input.

Geology, alteration, mineralization and geochemical study in Kalateh Taimour area, NE Iran

Directory of Open Access Journals (Sweden)

Zahra Alaminia

2010-11-01

Full Text Available The area is located 20 km northwest of Kashmar and about 4 km of Kalateh Taimour in Khorasan Razavi province. The study area is part of Tertiary volcanic-plutonic belt north of Daruneh fault and its situation in tectonic inliers between two important active faults, Doruneh and Taknar. Volcanic rocks are mainly intermediate to acid pyroclastic type. They formed during early Tertiary. The volcanic rocks of the Kalateh Taimour area are predominantly andesitic basalt, andesite, latite, trachyte, dacite and rhyodacite and are observed as lava, tuff, lapilli tuff and agglomerate. Field evidences and study show several subvolcanic bodies including quartz hornblende biotite monzodiorite porphyry, quartz biotite monzodiorite porphyry, quartz diorite porphyry and microdiorite which are intruded sometime in mid-Tertiary. In this belt, new methods of image processing were used for enhancing the alteration zones to help near infra red and short wavelength infrared and bands example band ratios and principle component method. Propylitic, sericitic and argillic are the main alteration types. Minor silicification is found in some areas. Alteration is extent but mineralization is limited. Mineralization is mainly controlled by fault system. Several mineralized faults are being discovered. Open space filling features are abundant. In the study area, disseminate and stock work mineralization are abundant. The amount of sulfide minerals is very small. Ancient mining is present in the area. Stream sediment geochemical study shows a very broad and high level of gold anomaly. Rock geochemical study show very high levels of Au, Ag, Cu, Pb, Zn and Au value is correlative to Cu, Pb, Zn and Ag values. Due to alteration modeling, non uniformity in mineralization and low abundance of sulfide mineralization suggest study in low sulphidation Au-Cu deposit.

Epithermal neutron instrumentation at ISIS

International Nuclear Information System (INIS)

Gorini, G; Festa, G; Andreani, C

2014-01-01

The advent of pulsed neutron sources makes available high epithermal neutron fluxes (in the energy range between 500 meV and 100 eV). New dedicated instrumentation, such as Resonance Detectors, was developed at ISIS spallation neutron source in the last years to apply the specific properties of this kind of neutron beam to the study of condensed matter. New detection strategies like Filter Difference method and Foil Cycling Technique were also developed in parallel to the detector improvement at the VESUVIO beamline. Recently, epithermal neutron beams were also used at the INES beamline to study elemental and isotopic composition of materials, with special application to cultural heritage studies. In this paper we review a series of epithermal neutron instrumentation developed at ISIS, their evolution over time and main results obtained

Composite particle production in relativistic Au+Au collisions at AGS: First results from the E866 forward spectrometer at sign 2, 4, and 10.8 A·GeV

International Nuclear Information System (INIS)

Ashktorab, K.

1996-01-01

Particle spectra were measured for Au + Au collisions at 2, 4, and 10. 8 A·GeV using the E866 spectrometers. Recent results on proton emission and composite particle production form the E866 forward spectrometer data taken in 1994 together with the first results from the 1995/6 AGS running period are presented. Preliminary results indicate a decrease in the coalescence scaling coefficient with increasing projectile energy and centrality

Compatibility between Co-Metallized PbTe Thermoelectric Legs and an Ag-Cu-In Brazing Alloy.

Science.gov (United States)

Ben-Ayoun, Dana; Sadia, Yatir; Gelbstein, Yaniv

2018-01-10

In thermoelectric (TE) generators, maximizing the efficiency of conversion of direct heat to electricity requires the reduction of any thermal and electrical contact resistances between the TE legs and the metallic contacts. This requirement is especially challenging in the development of intermediate to high-temperature TE generators. PbTe-based TE materials are known to be highly efficient up to temperatures of around 500 °C; however, only a few practical TE generators based on these materials are currently commercially available. One reason for that is the insufficient bonding techniques between the TE legs and the hot-side metallic contacts. The current research is focused on the interaction between cobalt-metallized n -type 9.104 × 10 -3 mol % PbI₂-doped PbTe TE legs and the Ag 0.32 Cu 0.43 In 0.25 brazing alloy, which is free of volatile species. Clear and fine interfaces without any noticeable formation of adverse brittle intermetallic compounds were observed following prolonged thermal treatment testing. Moreover, a reasonable electrical contact resistance of ~2.25 mΩmm² was observed upon brazing at 600 °C, highlighting the potential of such contacts while developing practical PbTe-based TE generators.

Comparison of optical transients during the picosecond laser pulse-induced crystallization of GeSbTe and AgInSbTe phase-change thin films: Nucleation-driven versus growth-driven processes

Energy Technology Data Exchange (ETDEWEB)

Liang, Guangfei [Key Laboratory of High Power Laser Materials, Shanghai Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, Shanghai 201800 (China); Li, Simian [State Key Laboratory of Optoelectronic Materials and Technology, Department of Physics, Sun Yat-Sen University, Guangzhou 510275 (China); Huang, Huan [Key Laboratory of High Power Laser Materials, Shanghai Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, Shanghai 201800 (China); Wang, Yang, E-mail: ywang@siom.ac.cn [Key Laboratory of High Power Laser Materials, Shanghai Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, Shanghai 201800 (China); Lai, Tianshu, E-mail: stslts@mail.sysu.edu.cn [State Key Laboratory of Optoelectronic Materials and Technology, Department of Physics, Sun Yat-Sen University, Guangzhou 510275 (China); Wu, Yiqun [Key Laboratory of High Power Laser Materials, Shanghai Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, Shanghai 201800 (China)

2013-09-01

Direct comparison of the real-time in-situ crystallization behavior of as-deposited amorphous Ge{sub 2}Sb{sub 2}Te{sub 5} (GeSbTe) and Ag{sub 8}In{sub 14}Sb{sub 55}Te{sub 23} (AgInSbTe) phase-change thin films driven by picosecond laser pulses was performed by a time-resolved optical pump-probe technique with nanosecond resolution. Different optical transients showed various crystallization processes because of the dissimilar nucleation- and growth-dominated mechanisms of the two materials. The effects of laser pulse fluence, thermal conductive structure, and successive pulse irradiation on their crystallization dynamics were also discussed. A schematic was then established to describe the different crystallization processes beginning from the as-deposited amorphous state. The results may provide further insight into the phase-change mechanism under extra-non-equilibrium conditions and aid the development of ultrafast phase-change memory materials.

Development of microstructured large area magnetic calorimeters with Au:Er- and Ag:Er-sensors for the detection of x-ray quanta and high energetic particles; Entwicklung grossflaechiger mikrostrukturierter magnetischer Kalorimeter mit Au:Er- und Ag:Er-Sensoren fuer den energieaufgeloesten Nachweis von Roentgenquanten und hochenergetischen Teilchen

Energy Technology Data Exchange (ETDEWEB)

Burck, Andreas

2008-11-04

This thesis describes the development of large-area magnetic calorimeters which could for example be used for the investigation of the dissociative recombination or the measurement of the Lamb-shift for hydrogenlike heavy ions. The detectors consist of two meandershaped niobium thin film pickup coils and a paramagnetic sensor. The deposition of energy in the sensor results in a temperature change and therefore in a change of magnetisation of the sensor, which can be measured by a SQUID-magnetometer with high precision. As sensormaterials a dilute alloy of gold-erbium (Au:Er) as well as silver-erbium (Ag:Er) were used. Whereas the Ag:Er-sensor was glued on the pickup coil the Au:Er-sensor was for the first time microstructured by a novel microstructuring process established in this thesis. For the characterisation of the detectors and the sensormaterials a fluorescence source and a {sup 55}Fe source were used. The thermodynamic properties of the Au:Er-sensors thereby show promising results, as the magnetisation shows bulk properties down to 20 mK. The measurements of the signalize and the magnetisation with the detector which was equipped with a Ag:Er-sensor showed that the thermodynamic properties of the Ag:Eralloy could be fully described. Furthermore the shape of the pulses, the noise and the energy resolution of both detectors will be discussed. (orig.)

The Shear Strength and Fracture Behavior of Sn-Ag- xSb Solder Joints with Au/Ni-P/Cu UBM

Science.gov (United States)

Lee, Hwa-Teng; Hu, Shuen-Yuan; Hong, Ting-Fu; Chen, Yin-Fa

2008-06-01

This study investigates the effects of Sb addition on the shear strength and fracture behavior of Sn-Ag-based solders with Au/Ni-P/Cu underbump metallization (UBM) substrates. Sn-3Ag- xSb ternary alloy solder joints were prepared by adding 0 wt.% to 10 wt.% Sb to a Sn-3.5Ag alloy and joining them with Au/Ni-P/Cu UBM substrates. The solder joints were isothermally stored at 150°C for up to 625 h to study their microstructure and interfacial reaction with the UBM. Single-lap shear tests were conducted to evaluate the mechanical properties, thermal resistance, and failure behavior. The results show that UBM effectively suppressed intermetallic compound (IMC) formation and growth during isothermal storage. The Sb addition helped to refine the Ag3Sn compounds, further improving the shear strength and thermal resistance of the solders. The fracture behavior evolved from solder mode toward the mixed mode and finally to the IMC mode with increasing added Sb and isothermal storage time. However, SnSb compounds were found in the solder with 10 wt.% Sb; they may cause mechanical degradation of the solder after long-term isothermal storage.

Polarized epithermal neutron spectrometer at KENS

International Nuclear Information System (INIS)

Kohgi, M.

1983-01-01

A spectrometer employing a white, epithermal, polarized neutron beam is under construction at KENS. The neutron polarization is achieved by passage through a dynamically polarized proton filter (DPPF). The results of the test experiments show that the DPPF method is promising in obtaining polarized epithermal neutron beam. The basic design of the spectrometer is described

Cube-like Fe3O4@SiO2@Au@Ag magnetic nanoparticles: a highly efficient SERS substrate for pesticide detection

Science.gov (United States)

Sun, Mei; Zhao, Aiwu; Wang, Dapeng; Wang, Jin; Chen, Ping; Sun, Henghui

2018-04-01

As a novel surface-enhanced Raman spectroscopic (SERS) nanocomposite, cube-like Fe3O4@SiO2@Au@Ag magnetic nanoparticles (NPs) were synthesized for the first time. Cube-like α-Fe2O3 NPs with uniform size were achieved by optimizing reaction temperature and time. Firstly, the cube-like Fe3O4@SiO2 with good dispersity was achieved by calcining α-Fe2O3@SiO2 NPs in hydrogen atmosphere at 360 °C for 2.5 h, followed by self-assembling a PEI shell via sonication. Furthermore, the Au@Ag particles were densely assembled on the Fe3O4@SiO2 NPs to form the Fe3O4@SiO2@Au@Ag composite structure via strong Ag-N interaction. The obtained nanocomposites exhibited an excellent SERS behavior, reflected by the low detection of limit (p-ATP) at the 5 × 10-14 M level. Moreover, these nanocubes were used for the detection of thiram, and the detection limit can reach 5 × 10-11 M. Meanwhile, the U.S. Environmental Protection Agency specifies that the residue in fruit must be lower than 7 ppm. Hence, the resulting substrate with high SERS activity has great practical potential applications in the rapid detection of chemical, biological, and environment pollutants with a simple portable Raman instrument at trace level.

Arrays of Ag and Au nanoparticles with terpyridine- and thiophene-based ligands: morphology and optical responses

Czech Academy of Sciences Publication Activity Database

Prusková, M.; Sutrová, V.; Šlouf, Miroslav; Vlčková, B.; Vohlídal, J.; Šloufová, I.

2017-01-01

Roč. 33, č. 17 (2017), s. 4146-4156 ISSN 0743-7463 R&D Projects: GA ČR(CZ) GAP108/12/1143 Institutional support: RVO:61389013 Keywords : nanocomposite monolayers * self-assembly * Ag and Au arrays Subject RIV: CD - Macromolecular Chemistry OBOR OECD: Polymer science Impact factor: 3.833, year: 2016

Neutron activation analysis of gold and prospectiveness of its application

International Nuclear Information System (INIS)

Tong Chunhan.

1988-01-01

NAA of gold is a method of high sensitivity and high percision, especially when epithermal neutron activation is applied. NAA is particularly emphasized in the process of gold reference standards preparation. In addition to the pure instrumental NAA, the NAA with pre-enrichment before sctivation is developed. This technque has been successfully used in assessment of micro and fine grained Au-Ag-phlymetal ores in Guixian, Guangxi. Through this example, prospectiveness of NAA application in Au-Ag-prospecting, fast assessment and trace element geochemistry investigation is seen

Electrical properties of Au/CdZnTe/Au detectors grown by the boron oxide encapsulated Vertical Bridgman technique

Energy Technology Data Exchange (ETDEWEB)

Turturici, A.A. [Dipartimento di Fisica e Chimica, Università di Palermo, Viale delle Scienze, Edificio 18, Palermo 90128 (Italy); Abbene, L., E-mail: leonardo.abbene@unipa.it [Dipartimento di Fisica e Chimica, Università di Palermo, Viale delle Scienze, Edificio 18, Palermo 90128 (Italy); Gerardi, G. [Dipartimento di Fisica e Chimica, Università di Palermo, Viale delle Scienze, Edificio 18, Palermo 90128 (Italy); Benassi, G. [due2lab s.r.l., Via Paolo Borsellino 2, Scandiano, 42019 Reggio Emilia (Italy); Bettelli, M.; Calestani, D. [IMEM/CNR, Parco Area delle Scienze 37/A, Parma 43100 (Italy); Zambelli, N. [due2lab s.r.l., Via Paolo Borsellino 2, Scandiano, 42019 Reggio Emilia (Italy); Raso, G. [Dipartimento di Fisica e Chimica, Università di Palermo, Viale delle Scienze, Edificio 18, Palermo 90128 (Italy); Zappettini, A. [IMEM/CNR, Parco Area delle Scienze 37/A, Parma 43100 (Italy); Principato, F. [Dipartimento di Fisica e Chimica, Università di Palermo, Viale delle Scienze, Edificio 18, Palermo 90128 (Italy)

2016-09-11

In this work we report on the results of electrical characterization of new CdZnTe detectors grown by the Boron oxide encapsulated Vertical Bridgman technique (B-VB), currently produced at IMEM-CNR (Parma, Italy). The detectors, with gold electroless contacts, have different thicknesses (1 and 2.5 mm) and the same electrode layout, characterized by a central anode surrounded by a guard-ring electrode. Investigations on the charge transport mechanisms and the electrical contact properties, through the modeling of the measured current–voltage (I–V) curves, were performed. Generally, the detectors are characterized by low leakage currents at high bias voltages even at room temperature: 34 nA/cm{sup 2} (T=25 °C) at 10,000 V/cm, making them very attractive for high flux X-ray measurements, where high bias voltage operation is required. The Au/CdZnTe barrier heights of the devices were estimated by using the interfacial layer-thermionic-diffusion (ITD) model in the reverse bias voltage range. Comparisons with CdZnTe detectors, grown by Traveling Heater Method (THM) and characterized by the same electrode layout, deposition technique and resistivity, were also performed.

Super-resolution by elliptical bubble formation with PtOx and AgInSbTe layers

International Nuclear Information System (INIS)

Kim, Jooho; Hwang, Inoh; Yoon, Duseop; Park, Insik; Shin, Dongho; Kikukawa, Takashi; Shima, Takayuki; Tominaga, Junji

2003-01-01

The recording and retrieval of signals below 100 nm mark length were attempted with elliptical bubble-type super-resolution technology with platinum oxide (PtO x ) and ductile AgInSbTe layers, using the same optical system as that of a digital versatile disk (a 635 nm wavelength red laser system). The carrier-to-noise ratio (CNR) of over 47 dB for 100 nm mark length signals (over 43 dB for 80 nm mark length signals) was obtained, which can be considered as a commercially acceptable level of CNR. The recording mechanism of the sample disk was shown through the transmission electron microscopy cross-section image observation to be by rigid elliptical bubble formation at the PtO x layer located between the AgInSbTe layers. The results of this report represent the potential for a much higher-density storage using the red laser system and a subterabyte optical storage using the blue laser system

A ternary functional Ag@GO@Au sandwiched hybrid as an ultrasensitive and stable surface enhanced Raman scattering platform

Science.gov (United States)

Zhang, Cong-yun; Hao, Rui; Zhao, Bin; Hao, Yao-wu; Liu, Ya-qing

2017-07-01

The graphene-mediated surface enhanced Raman scattering (SERS) substrates by virtues of plasmonic metal nanostructures and graphene or its derivatives have attracted tremendous interests which are expected to make up the deficiency of traditional plasmonic metal substrates. Herein, we designed and fabricated a novel ternary Ag@GO@Au sandwich hybrid wherein the ultrathin graphene oxide (GO) films were seamlessly wrapped around the hierarchical flower-like Ag particle core and meanwhile provided two-dimensional anchoring scaffold for the coating of Au nanoparticles (NPs). The surface coverage density of loading Au NPs could be readily controlled by tuning the dosage amount of Au particle solutions. These features endowed the sandwiched structures high enrichment capability for analytes such as aromatic molecules and astonishing SERS performance. The Raman signals were enormously enhanced with an ultrasensitive detection limit of rhodamine-6G (R6G) as low as 10-13 M based on the chemical enhancement from GO and multi-dimensional plasmonic coupling between the metal nanoparticles. In addition, the GO interlayer as an isolating shell could effectively prevent the metal-molecule direct interaction and suppress the oxidation of Ag after exposure at ambient condition which enabled the substrates excellent reproducibility with less than 6% signal variations and prolonged life-time. To evaluate the feasibility and the practical application for SERS detection in real-world samples based on GO sandwiched hybrid as SERS-active substrate, three different prohibited colorants with a series of concentrations were measured with a minimum detected concentration down to 10-9 M. Furthermore, the prepared GO sandwiched nanostructures can be used to identify different types of colorants existing in red wine, implying the great potential applications for single-particle SERS sensing of biotechnology and on-site monitoring in food security.

Effect of the Fabrication Parameters of the Nanosphere Lithography Method on the Properties of the Deposited Au-Ag Nanoparticle Arrays.

Science.gov (United States)

Liu, Jing; Chen, Chaoyang; Yang, Guangsong; Chen, Yushan; Yang, Cheng-Fu

2017-04-03

The nanosphere lithography (NSL) method can be developed to deposit the Au-Ag triangle hexagonal nanoparticle arrays for the generation of localized surface plasmon resonance. Previously, we have found that the parameters used to form the NSL masks and the physical methods required to deposit the Au-Ag thin films had large effects on the geometry properties of the nanoparticle arrays. Considering this, the different parameters used to grow the Au-Ag triangle hexagonal nanoparticle arrays were investigated. A single-layer NSL mask was formed by using self-assembly nano-scale polystyrene (PS) nanospheres with an average radius of 265 nm. At first, the concentration of the nano-scale PS nanospheres in the solution was set at 6 wt %. Two coating methods, drop-coating and spin-coating, were used to coat the nano-scale PS nanospheres as a single-layer NSL mask. From the observations of scanning electronic microscopy (SEM), we found that the matrixes of the PS nanosphere masks fabricated by using the drop-coating method were more uniform and exhibited a smaller gap than those fabricated by the spin-coating method. Next, the drop-coating method was used to form the single-layer NSL mask and the concentration of nano-scale PS nanospheres in a solution that was changed from 4 to 10 wt %, for further study. The SEM images showed that when the concentrations of PS nanospheres in the solution were 6 and 8 wt %, the matrixes of the PS nanosphere masks were more uniform than those of 4 and 10 wt %. The effects of the one-side lifting angle of substrates and the vaporization temperature for the solvent of one-layer self-assembly PS nanosphere thin films, were also investigated. Finally, the concentration of the nano-scale PS nanospheres in the solution was set at 8 wt % to form the PS nanosphere masks by the drop-coating method. Three different physical deposition methods, including thermal evaporation, radio-frequency magnetron sputtering, and e-gun deposition, were used to

Effect of the Fabrication Parameters of the Nanosphere Lithography Method on the Properties of the Deposited Au-Ag Nanoparticle Arrays

Directory of Open Access Journals (Sweden)

Jing Liu

2017-04-01

Full Text Available The nanosphere lithography (NSL method can be developed to deposit the Au-Ag triangle hexagonal nanoparticle arrays for the generation of localized surface plasmon resonance. Previously, we have found that the parameters used to form the NSL masks and the physical methods required to deposit the Au-Ag thin films had large effects on the geometry properties of the nanoparticle arrays. Considering this, the different parameters used to grow the Au-Ag triangle hexagonal nanoparticle arrays were investigated. A single‐layer NSL mask was formed by using self‐assembly nano-scale polystyrene (PS nanospheres with an average radius of 265 nm. At first, the concentration of the nano-scale PS nanospheres in the solution was set at 6 wt %. Two coating methods, drop-coating and spin-coating, were used to coat the nano-scale PS nanospheres as a single‐layer NSL mask. From the observations of scanning electronic microscopy (SEM, we found that the matrixes of the PS nanosphere masks fabricated by using the drop-coating method were more uniform and exhibited a smaller gap than those fabricated by the spin-coating method. Next, the drop-coating method was used to form the single‐layer NSL mask and the concentration of nano-scale PS nanospheres in a solution that was changed from 4 to 10 wt %, for further study. The SEM images showed that when the concentrations of PS nanospheres in the solution were 6 and 8 wt %, the matrixes of the PS nanosphere masks were more uniform than those of 4 and 10 wt %. The effects of the one-side lifting angle of substrates and the vaporization temperature for the solvent of one-layer self-assembly PS nanosphere thin films, were also investigated. Finally, the concentration of the nano-scale PS nanospheres in the solution was set at 8 wt % to form the PS nanosphere masks by the drop-coating method. Three different physical deposition methods, including thermal evaporation, radio-frequency magnetron sputtering, and e

Chiral recognition of phenylglycinol enantiomers based on N-acetyl-L-cysteine capped CdTe quantum dots in the presence of Ag+

Science.gov (United States)

Guo, Yuan; Zeng, Xiaoqing; Yuan, Haiyan; Huang, Yunmei; Zhao, Yanmei; Wu, Huan; Yang, Jidong

2017-08-01

In this study, a novel method for chiral recognition of phenylglycinol (PG) enantiomers was proposed. Firstly, water-soluble N-acetyl-L-cysteine (NALC)-capped CdTe quantum dots (QDs) were synthesized and experiment showed that the fluorescence intensity of the reaction system slightly enhancement when added PG enantiomers to NALC-capped CdTe quantum dots (QDs), but the R-PG and S-PG could not be distinguished. Secondly, when there was Ag+ presence in the reaction system, the experiment result was extremely interesting, the PG enantiomers cloud make NALC-capped CdTe QDs produce different fluorescence signal, in which the fluorescence of S-PG + Ag+ + NALC-CdTe system was significantly enhanced, and the fluorescence of R-PG + Ag+ + NALC-CdTe system was markedly decreased. Thirdly, all the enhanced and decreased of the fluorescence intensity were directly proportional to the concentration of R-PG and S-PG in the linearly range 10- 5-10- 7 mol·L- 1, respectively. So, the new method for simultaneous determination of the PG enantiomers was built too. The experiment result of the method was satisfactory with the detection limit of PG can reached 10- 7 mol·L- 1 and the related coefficient of S-PG and R-PG are 0.995 and 0.980, respectively. The method was highly sensitive, selective and had wider detection range compared with other methods.

40Ar-39Ar dating of Archean iron oxide Cu-Au and Paleoproterozoic granite-related Cu-Au deposits in the Carajás Mineral Province, Brazil: implications for genetic models

Science.gov (United States)

Pollard, Peter J.; Taylor, Roger G.; Peters, Lisa; Matos, Fernando; Freitas, Cantidiano; Saboia, Lineu; Huhn, Sergio

2018-05-01

40Ar-39Ar dating of biotite from IOCG and granite-related Cu-Au deposits in the Carajás Mineral Province provides evidence for the timing of mineralization and constraints on genetic models of ore formation. Ages of biotite from greisen and quartz-rich vein and breccia deposits, Alvo 118—1885 ± 4 Ma, Breves—1886 ± 5 Ma, Estrela—1896 ± 7 Ma, and Gameleira—1908 ± 7 Ma, demonstrate the close temporal relationship between Cu-Au mineralization and subjacent A-type granites. Mineralization is hosted within granite cupolas (Breves) or in vein/breccia systems emanating from the cupolas (Estrela and Gameleira), consistent with a genetic relationship of mineralization to the B-Li-F-rich granites. Plateau and minimum ages of biotite from IOCG deposits, including Igarapé Bahia, Cristalino, Corta Goela, and GT34, range from 2537 ± 6 Ma to 2193 ± 4 Ma. The 40Ar-39Ar age of biotite from Igarapé Bahia (2537 ± 6 Ma) is similar to a previous SHRIMP 207Pb-206Pb age for monazite of 2575 ± 12 Ma when the uncertainties in the respective analyses and standards are taken into account. The age spectrum for biotite from Cristalino shows increasing ages for successive steps, consistent with post-crystallization Ar loss, and the age of 2388 ± 5 Ma for the last three steps is considered a minimum age for Cu-Au mineralization. The age of biotite from the GT34 prospect (2512 ± 7 Ma) coincides with a previously identified period of basement reactivation and may indicate the formation of Cu-Au mineralization at this time or resetting of biotite from an older mineralization event at this time. At Corta Goela, within the Canaã Shear Zone, the biotite age of 2193 ± 4 Ma lies between the ages of IOCG (2.57-2.76 Ga) and granite-related Cu-Au ( 1.88 Ga) deposits elsewhere in the Carajás district but is similar to previously reported 40Ar-39Ar ages for amphibole from Sossego, possibly indicating that mineralization at both Sossego and Corta Goela was affected by a thermal event at

Energy-resolved attosecond interferometric photoemission from Ag(111) and Au(111) surfaces

Science.gov (United States)

Ambrosio, M. J.; Thumm, U.

2018-04-01

Photoelectron emission from solid surfaces induced by attosecond pulse trains into the electric field of delayed phase-coherent infrared (IR) pulses allows the surface-specific observation of energy-resolved electronic phase accumulations and photoemission delays. We quantum-mechanically modeled interferometric photoemission spectra from the (111) surfaces of Au and Ag, including background contributions from secondary electrons and direct emission by the IR pulse, and adjusted parameters of our model to energy-resolved photoelectron spectra recently measured at a synchrotron light source by Roth et al. [J. Electron Spectrosc. 224, 84 (2018), 10.1016/j.elspec.2017.05.008]. Our calculated spectra and photoelectron phase shifts are in fair agreement with the experimental data of Locher et al. [Optica 2, 405 (2015), 10.1364/OPTICA.2.000405]. Our model's not reproducing the measured energy-dependent oscillations of the Ag(111) photoemission phases may be interpreted as evidence for subtle band-structure effects on the final-state photoelectron-surface interaction not accounted for in our simulation.

Synthesis and Optical Properties of Au-Ag Alloy Nanoclusters with Controlled Composition

Directory of Open Access Journals (Sweden)

J. F. Sánchez-Ramírez

2008-01-01

Full Text Available Colloidal solid-solution-like Au-Ag alloy nanoclusters of different compositions were synthesized through citrate reduction of mixed metal ions of low concentrations, without using any other protective or capping agents. Optical absorption of the alloy nanoclusters was studied both theoretically and experimentally. The position of the surface plasmon resonance (SPR absorption band of the nanoclusters could be tuned from 419 nm to 521 nm through the variation of their composition. Considering effective dielectric constant of the alloy, optical absorption spectra for the nanoclusters were calculated using Mie theory, and compared with the experimentally obtained spectra. Theoretically obtained optical spectra well resembled the experimental spectra when the true size distribution of the nanoparticles was considered. High-resolution transmission electron microscopy (HREM, high-angle annular dark field (HAADF imaging, and energy dispersive spectroscopy (EDS revealed the true alloy nature of the nanoparticles with nominal composition being preserved. The synthesis technique can be extended to other bimetallic alloy nanoclusters containing Ag.

Contrasting fluids and reservoirs in the contiguous Marcona and Mina Justa iron oxide-Cu (-Ag-Au) deposits, south-central Perú

Science.gov (United States)

Chen, Huayong; Kyser, T. Kurtis; Clark, Alan H.

2011-10-01

The Marcona-Mina Justa deposit cluster, hosted by Lower Paleozoic metaclastic rocks and Middle Jurassic shallow marine andesites, incorporates the most important known magnetite mineralization in the Andes at Marcona (1.9 Gt at 55.4% Fe and 0.12% Cu) and one of the few major iron oxide-copper-gold (IOCG) deposits with economic Cu grades (346.6 Mt at 0.71% Cu, 3.8 g/t Ag and 0.03 g/t Au) at Mina Justa. The Middle Jurassic Marcona deposit is centred in Ica Department, Perú, and the Lower Cretaceous Mina Justa Cu (Ag, Au) prospect is located 3-4 km to the northeast. New fluid inclusion studies, including laser ablation time-of-flight inductively coupled plasma mass spectrometry (LA-TOF-ICPMS) analysis, integrated with sulphur, oxygen, hydrogen and carbon isotope analyses of minerals with well-defined paragenetic relationships, clarify the nature and origin of the hydrothermal fluid responsible for these contiguous but genetically contrasted deposits. At Marcona, early, sulphide-free stage M-III magnetite-biotite-calcic amphibole assemblages are inferred to have crystallized from a 700-800°C Fe oxide melt with a δ18O value from +5.2‰ to +7.7‰. Stage M-IV magnetite-phlogopite-calcic amphibole-sulphide assemblages were subsequently precipitated from 430-600°C aqueous fluids with dominantly magmatic isotopic compositions (δ34S = +0.8‰ to +5.9‰; δ18O = +9.6‰ to +12.2‰; δD = -73‰ to -43‰; and δ13C = -3.3‰). Stages M-III and M-IV account for over 95% of the magnetite mineralization at Marcona. Subsequent non-economic, lower temperature sulphide-calcite-amphibole assemblages (stage M-V) were deposited from fluids with similar δ34S (+1.8‰ to +5.0‰), δ18O (+10.1‰ to +12.5‰) and δ13C (-3.4‰), but higher δD values (average -8‰). Several groups of lower (200°C) fluids can be recognized in the main polymetallic (Cu, Zn, Pb) sulphide stage M-V and may record the involvement of modified seawater. At Mina Justa, early magnetite

Theoretical study of PTCDA adsorbed on the coinage metal surfaces, Ag(111), Au(111) and Cu(111)

International Nuclear Information System (INIS)

Romaner, L; Nabok, D; Puschnig, P; Ambrosch-Draxl, C; Zojer, E

2009-01-01

A thorough understanding of the adsorption of molecules on metallic surfaces is a crucial prerequisite for the development and improvement of functionalized materials. A prominent representative within the class of π-conjugated molecules is 3,4,9,10-perylene-tetracarboxylic acid dianhydride (PTCDA) which, adsorbed on the Ag(111), Au(111) or Cu(111) surfaces, shows characteristic trends for work-function modification, alignment of molecular levels with the substrate Fermi energy and binding distances. We carried out density functional theory (DFT) calculations to investigate to what extent these trends can be rationalized on a theoretical basis. We used different density functionals (DF) including a fully non-local van der Waals (vdW) DF capable of describing dispersion interactions. We show that, rather independent of the DF, the calculations yield level alignments and work-function modifications consistent with ultra-violet photoelectron spectroscopy when the monolayer is placed onto the surfaces at the experimental distances (as determined from x-ray standing wave experiments). The lowest unoccupied molecular orbital is occupied on the Ag and Cu surfaces, whereas it remains unoccupied on the Au surface. Simultaneously, the work function increases for Ag but decreases for Cu and Au. Adsorption distances and energies, on the other hand, depend very sensitively on the choice of the DF. While calculations in the local density approximation bind the monolayer consistently with the experimental trends, the generalized gradient approximation in several flavors fails to reproduce realistic distances and energies. Calculations employing the vdW-DF reveal that substantial bonding contributions arise from dispersive interactions. They yield reasonable binding energies but larger binding distances than the experiments.

Neutron Capture Gamma Ray Cross Sections for Ta, Ag, In and Au between 30 and 175 keV

Energy Technology Data Exchange (ETDEWEB)

Hellstroem, J; Beshai, S

1971-11-15

A new detector has been used to determine neutron capture gamma ray cross sections for Ta, Ag, In and Au. The results are listed and discussed together with associated problems. The energy range from 30 keV to 175 keV is considered

Neutron Capture Gamma Ray Cross Sections for Ta, Ag, In and Au between 30 and 175 keV

International Nuclear Information System (INIS)

Hellstroem, J.; Beshai, S.

1971-11-01

A new detector has been used to determine neutron capture gamma ray cross sections for Ta, Ag, In and Au. The results are listed and discussed together with associated problems. The energy range from 30 keV to 175 keV is considered

The occurrence of ferropyrosmalite in the mineralized breccias from Igarape Bahia (North region, Brazil) Au-Cu (± ETR-U) deposit, Carajas mineral Province

International Nuclear Information System (INIS)

Tazava, Edison; Gomes, Newton Souza; Oliveira, Claudinei Gouveia de

1999-01-01

In the last years, several works report the presence of pyrosmalite mineral series [(Fe, Mn) 8 Si 6 O 15 (OH, Cl) 10 ] commonly associated with volcanic exhalative massive sulphide or Fe-Mn metamorphosed deposits. In this paper, we present the inedit occurrence of ferropyrosmalite in the Au-Cu (± REE-U) of Igarape Bahia deposit, located in the Au-Cu district of the Carajas Mineral Province. We consider the Igarape Bahia mineralization as being related to the genesis of iron-oxide class deposit, like the Olympic Dam type. Ferropyrosmalite occurs in two different contexts: associated with carbonate veins; associated with heterolithic breccias, composed by BIF and mafic metavolcanic fragments immersed in a magnetic, chalcopyrite, bornite, pyrite, carbonates (calcite to siderite), uranium and REE minerals, and gold, - rich matrix. The growth of ferropyrosmalite is probably due to the substitution of iron rich minerals (chloride, magnetite and siderite), controlled by magmatic fluid influx rich in chlorine. The permeability of breccias and the discontinuity of veins favour fluid percolation. The mode of occurrence of ferropyrosmalite and its relation with amphibole (ferro-hornblende-actinolite) indicate metasomatic growth of the former under temperatures in the transition of greenschist/amphibolite facies. The ferropyrosmalite of the Igarape Bahia deposit represents an uncommon type of occurrence linked to hydrothermal/magmatic conditions. (author)

Effects of plasmon excitation on photocatalytic activity of Ag/TiO 2 and Au/TiO2 nanocomposites

DEFF Research Database (Denmark)

Sellappan, Raja; González-Posada, Fernando; Chakarov, Dinko

2013-01-01

Model nanocomposite photocatalysts consisting of undoped TiO2 films with optically active Ag or Au nanoparticles (NPs) were designed, fabricated, and examined to address the role of plasmon excitations in their performance. Different composition configurations were tested in which the NPs were ei...

Gold and palladium minerals (including empirical PdCuBiSe3) from the former Roter Bär mine, St. Andreasberg, Harz Mountains, Germany: a result of low-temperature, oxidising fluid overprint

Science.gov (United States)

Cabral, Alexandre Raphael; Ließmann, Wilfried; Lehmann, Bernd

2015-10-01

At Roter Bär, a former underground mine in the polymetallic deposits of St. Andreasberg in the middle-Harz vein district, Germany, native gold and palladium minerals occur very locally in clausthalite-hematite pockets of few millimetres across in carbonate veinlets. The native gold is a Au-Ag intermetallic compound and the palladium minerals are characterised as mertieite-II [Pd8(Sb,As)3] and empirical PdCuBiSe3 with some S. The latter coexists with bohdanowiczite (AgBiSe2), a mineral that is stable below 120 °C. The geological setting of Roter Bär, underneath a post-Variscan unconformity, and its hematite-selenide-gold association suggest that oxidising hydrothermal brines of low temperature were instrumental to the Au-Pd mineralisation. The Roter Bär Au-Pd mineralisation can be explained by Permo-Triassic, red-bed-derived brines in the context of post-Variscan, unconformity-related fluid overprint.

Mineralogical, textural, sulfur and lead isotope constraints on the origin of Ag-Pb-Zn mineralization at Bianjiadayuan, Inner Mongolia, NE China

Science.gov (United States)

Zhai, Degao; Liu, Jiajun; Cook, Nigel J.; Wang, Xilong; Yang, Yongqiang; Zhang, Anli; Jiao, Yingchun

2018-04-01

The Bianjiadayuan Ag-Pb-Zn deposit (4.81 Mt. @157.4 g/t Ag and 3.94% Pb + Zn) is located in the Great Hinggan Range Pb-Zn-Ag-Cu-Mo-Sn-Fe polymetallic metallogenic belt, NE China. Vein type Pb-Zn-Ag ore bodies are primarily hosted by slate, adjacent to a Sn ± Cu ± Mo mineralized porphyry intrusion. The deposit is characterized by silver-rich ores with Ag grades up to 3000 g/t. Four primary paragenetic sequences are recognized: (I) arsenopyrite + pyrite + quartz, (II) main sulfide + quartz, (III) silver-bearing sulfosalt + quartz, and (IV) boulangerite + calcite. A subsequent supergene oxidation stage has also been identified. Hydrothermal alteration consists of an early episode of silicification, two intermediate episodes (propylitic and phyllic), and a late argillic episode. Silver mineralization primarily belongs to the late paragenetic sequence III. Freibergite is the dominant and most important Ag-mineral in the deposit. Detailed ore mineralogy of Bianjiadayuan freibergite reveals evidence of chemical heterogeneity down to the microscale. Silver-rich sulfosalts in the late paragenetic sequence III are largely derived from a series of retrograde and solid-state reactions that redistribute Ag via decomposition and exsolution during cooling, illustrating that documentation of post-mineralization processes is essential for understanding silver ore formation. Sulfur and lead isotope compositions of sulfides, and comparison with those of local various geological units, indicate that the ore-forming fluids, lead, and other metals have a magmatic origin, suggesting a close genetic association between the studied Ag-Pb-Zn veins and the local granitic intrusion. Fluid cooling coupled with decreases in fO2 and fS2 are the factors inferred to have led to a decrease of silver solubility in the hydrothermal fluid, and successively promoted extensive Ag deposition.

Correlation between magnetoresistance and magnetization in Ag Mn and Au Mn spin glasses

International Nuclear Information System (INIS)

Majumdar, A.K.

1982-08-01

Magnetization has been measured between 2 and 77 K and mostly up to fields of 20 K Oe in Ag Mn (1.1 and 5.4 at %) and Au Mn (1.8 and 4.6 at %) spin glass samples where the transverse magnetoresistance was measured earlier. It is found for the first time over a wide range of temperature and magnetic field that the negative magnetoresistance varies as the square of the bulk magnetization resulting in an universal curve in the spin glass regime. A theoretical justification is provided in terms of exciting theories. (author)

Size-controlled sensitivity and selectivity for the fluorometric detection of Ag+ by homocysteine capped CdTe quantum dots

International Nuclear Information System (INIS)

Jiao, Hangzhou; Liang, Zhenhua; Peng, Guihua; Zhang, Ling; Lin, Hengwei

2014-01-01

We have synthesized water dispersible CdTe quantum dots (QDs) in different sizes and with various capping reagents, and have studied the effects of their size on the sensitivity and selectivity in the fluorometric determination of metal ions, particularly of silver(I). It is found that an increase in the particle size of homocysteine-capped CdTe QDs from 1.7 nm to 3.3 nm and to 3.7 nm enhances both the sensitivity and selectivity of the determination of Ag(I) to give an ultimate limit of detection as low as 8.3 nM. This effect can partially be explained by the better passivation of surface traps on smaller sized QDs via adsorption of Ag(I), thereby decreasing the apparent detection efficiency. In addition, the presence of CdS in the CdTe QDs is likely to play a role. The study demonstrates that an improvement in sensing performance is accomplished by using QDs of fine-tuned particle sizes. Such effects are likely also to occur with other QD-based optical probes. (author)

Silver- and Zirconium-added ternary and quaternary TiAu based high temperature shape memory alloys

Energy Technology Data Exchange (ETDEWEB)

Wadood, A., E-mail: abdul.wadood@ist.edu.pk [High Temperature Materials Unit, National Institute for Materials Science, 1-2-1 Sengen, Tsukuba, Ibaraki 305-0047 (Japan); Department of Materials Science and Engineering, Institute of Space Technology (IST), Near Rawat Toll Plaza, Islamabad (Pakistan); Yamabe-Mitarai, Y. [High Temperature Materials Unit, National Institute for Materials Science, 1-2-1 Sengen, Tsukuba, Ibaraki 305-0047 (Japan)

2015-10-15

Low strength in B2 phase, incomplete shape memory effect and high cost of Au are obstacles for the use of Ti–50Au as a high temperature shape memory alloy. We investigated the effects of partial substitution of Ti with Zr and Au with Ag in Ti–Au on phase constitution, phase transformation, and high temperature thermo-mechanical and shape memory properties. Partial substitution of Ti with Zr in Ti–50Au and Ti–40Au–10Ag was found to improve the thermo-mechanical and shape memory effect. However, partial substitution of Au with Ag in Ti–50Au and Ti–50Au–10Zr was found to have negligible effects. Reasons for such different behavior of Zr- and Ag-added Ti–Au alloys are considered. - Highlights: • Au, Ag and Ti, Zr belong to same group. Effects of partial substitution of Au with Ag and Ti with Zr in Ti–Au are investigated. • Zr was found more effective than Ag in improving shape memory and mechanical properties. • Same atomic size of Au and Ag and large size misfit b/w Ti and Zr atoms. • Ag resulted large amount of precipitation in Ti–Au.

First principles-based adsorption comparison of group IV elements (C, Si, Ge, and Sn) on Au(111)/Ag(111) surface

International Nuclear Information System (INIS)

Chakraborty, Sudip; Rajesh, Ch.

2012-01-01

We have reported a first-principle investigation of the structural properties of monomer and dimer for group IV elements (C, Si, Ge, and Sn) adsorbed on the Au(111) and Ag(111) surfaces. The calculations were performed by means of a plane wave based pseudopotential method under the framework of density functional theory. The results reveal the preference of adatom to be adsorbed on the hexagonal closed packed site of the metal (111) surfaces with strong binding energy. The structures introduce interlayer forces in the adsorbate. The strong bonding with the surface atoms is a result of p–d hybridization. The adsorption energy follows a sequence as one goes down in the group IV elements which imply that the interaction of the group IV elements with Au/Ag is decreasing as the atomic number increases.

Photoproduced fluorescent Au(I)@(Ag2/Ag3)-thiolate giant cluster: an intriguing sensing platform for DMSO and Pb(II).

Science.gov (United States)

Ganguly, Mainak; Mondal, Chanchal; Jana, Jayasmita; Pal, Anjali; Pal, Tarasankar

2014-01-14

Synergistic evolution of fluorescent Au(I)@(Ag2/Ag3)-thiolate core-shell particles has been made possible under the Sun in presence of the respective precursor coinage metal compounds and glutathione (GSH). The green chemically synthesized fluorescent clusters are giant (∼600 nm) in size and robust. Among all the common water miscible solvents, exclusively DMSO exhibits selective fluorescence quenching (Turn Off) because of the removal of GSH from the giant cluster. Again, only Pb(II) ion brings back the lost fluorescence (Turn On) leaving aside all other metal ions. This happens owing to the strong affinity of the sulfur donor of DMSO for Pb(II). Thus, employing the aqueous solution containing the giant cluster, we can detect DMSO contamination in water bodies at trace level. Besides, a selective sensing platform has emerged out for Pb(II) ion with a detection limit of 14 × 10(-8) M. Pb(II) induced fluorescence recovery is again vanished by I(-) implying a promising route to sense I(-) ion.

Optical Property Characterization of Novel Graphene-X (X=Ag, Au and Cu Nanoparticle Hybrids

Directory of Open Access Journals (Sweden)

Sumit Ranjan Sahu

2013-01-01

Full Text Available The present investigation reports new results on optical properties of graphene-metal nanocomposites. These composites were prepared by a solution-based chemical approach. Graphene has been prepared by thermal reduction of graphene oxide (GO at 90°C by hydrazine hydrate in an ammoniacal medium. This ammoniacal solution acts as a solvent as well as a basic medium where agglomeration of graphene can be prevented. This graphene solution has further been used for functionalization with Ag, Au, and Cu nanoparticles (NPs. The samples were characterized by X-ray diffraction (XRD, Raman spectroscopy, UV-Vis spectroscopy, scanning electron microscopy (SEM, and transmission electron microscopy (TEM to reveal the nature and type of interaction of metal nanoparticles with graphene. The results indicate distinct shift of graphene bands both in Raman and UV-Vis spectroscopies due to the presence of the metal nanoparticles. Raman spectroscopic analysis indicates blue shift of D and G bands in Raman spectra of graphene due to the presence of metal nanoparticles except for the G band of Cu-G, which undergoes red shift, reflecting the charge transfer interaction between graphene sheets and metal nanoparticles. UV-Vis spectroscopic analysis also indicates blue shift of graphene absorption peak in the hybrids. The plasmon peak position undergoes blue shift in Ag-G, whereas red shift is observed in Au-G and Cu-G.

Elimination of eight interfering radioisotopes in the determination of uranium by activation analysis with epithermic neutrons

International Nuclear Information System (INIS)

Requejo, C.S.

1977-01-01

The total or parcial elimination interfering radioisotopes in activation analysis of uranium by epithermic neutrons, has been made. It was possible to determine uranium, after chemical separation, from samples of organic and mineral matrixes, which had mercury, selenium, bromine, antimony, gold, barium, molybden and tungsten. Mineral samples were analysed giving results between 0.2 to 5.0 ppm of uranium. The same mineral were ground in agate mortar and in tungsten carbide mill. In the first sample is has been found 0.2277 +- -+ 0.0474 ppm U. The second which had tungsten, at level of 150 ppm, after radiochemical separation, it has been found 0.2465+- -+0.0326 ppm U. These results are considered statistically the same [pt

Analysis of nanostructuring in high figure-of-merit Ag{sub 1-x}Pb{sub m}SbTe{sub 2+m} thermoelectric materials

Energy Technology Data Exchange (ETDEWEB)

Cook, Bruce A; Harringa, Joel L [Materials and Engineering Physics Program, Ames Laboratory, Iowa State University Ames, IA (United States); Kramer, Matthew J [Materials Science and Engineering, Iowa State University Ames, IA (United States); Han, Mi-Kyung [Department of Chemistry, Northwestern University Evanston, IL (United States); Chung, Duck-Young [Material Science Division, Argonne National Laboratory, IL (United States); Kanatzidis, Mercouri G [Department of Chemistry, Northwestern University Evanston, IL (United States); Material Science Division, Argonne National Laboratory, IL (United States)

2009-04-23

Thermoelectric materials based on quaternary compounds Ag{sub 1-x}Pb{sub m}SbTe{sub 2+m} exhibit high dimensionless figure-of-merit values, ranging from 1.5 to 1.7 at 700 K. The primary factor contributing to the high figure of merit is a low lattice thermal conductivity, achieved through nanostructuring during melt solidification. As a consequence of nucleation and growth of a second phase, coherent nanoscale inclusions form throughout the material, which are believed to result in scattering of acoustic phonons while causing only minimal scattering of charge carriers. Here, characterization of the nanosized inclusions in Ag{sub 0.53}Pb{sub 18}Sb{sub 1.2}Te{sub 20} that shows a strong tendency for crystallographic orientation along the {l_brace}001{r_brace} planes, with a high degree of lattice strain at the interface, consistent with a coherent interfacial boundary is reported. The inclusions are enriched in Ag relative to the matrix, and seem to adopt a cubic, 96 atom per unit cell Ag{sub 2}Te phase based on the Ti{sub 2}Ni type structure. In-situ high-temperature synchrotron radiation diffraction studies indicated that the inclusions remain thermally stable to at least 800 K. (Abstract Copyright [2009], Wiley Periodicals, Inc.)

Nicolas Lyon-Caen , La boîte à Perrette, le jansénisme parisien au xviiie siècle

OpenAIRE

Vermander, Benoît

2012-01-01

Nicolas Lyon-­­­Caen publie ici sa thèse sou­­te­­nue en 2008 à l’uni­­ver­­sité Paris I (dir. Cl. Mi­­­chaud) sous le titre Mar­­chands de miracles. La bour­­geoi­­sie jan­­sé­­niste pari­­sienne au xviiie siècle, elle-­­­même pro­­lon­­ge­­ment d’une thèse de l’École des Chartes consa­­crée au finan­­ce­­ment du « parti » jan­­sé­­niste au xviiie siècle (La boîte à Perrette, 2002). Ce n’est donc pas une his­­toire de l’ensemble des jan­­sé­­nistes pari­­siens que l’on trou­­vera dans cet ou...

Geochronological framework of the early Paleozoic Bainaimiao Cu-Mo-Au deposit, NE China, and its tectonic implications

Science.gov (United States)

Zhou, Zhen-Hua; Mao, Jing-Wen; Ma, Xing-Hua; Che, He-Wei; Ou'yang, He-Gen; Gao, Xu

2017-08-01

-Mo or Cu-Au mineralization and associated epithermal Au deposits.

The La Unión Au ± Cu prospect, Camagüey District, Cuba: fluid inclusion and stable isotope evidence for ore-forming processes

Science.gov (United States)

Santana, Miriela María Ulloa; Moura, Márcia Abrahão; Olivo, Gema R.; Botelho, Nilson Francisquini; Kyser, T. Kurtis; Bühn, Bernhard

2011-01-01

The Camagüey district, Cuba, is known for its epithermal precious metal deposits in a Cretaceous volcanic arc setting. Recently, the La Unión prospect was discovered in the southern part of the district, containing gold and minor copper mineralization interpreted as porphyry type. Mineralization is hosted in a 73.0 ± 1.5 Ma calc-alkaline I-type oxidized porphyry quartz diorite intrusive within volcanic and volcaniclastic rocks of the early Cretaceous Guáimaro Formation. The porphyry is affected by propylitic alteration and crosscut by a network of quartz and carbonate veinlets and veins. Chlorite, epidote, sericite, quartz, and pyrite are the main minerals in the early veins which are cut by late carbonate and zeolite veins. Late barite pseudomorphously replaces pyrite. Gold is associated with pyrite as disseminations in the altered quartz diorite and in the veins, occurring as inclusions or filling fractures in pyrite with 4 g/t Au in bulk samples, and up to 900 ppm Au in in pyrite. Fluid inclusion and oxygen isotope data are consistent with a H2O-NaCl-(KCl) mineralizing fluid, derived from the quartz diorite magma, and trapped at least at 425°C and 1.2 kbar. This primary fluid unmixed into two fluid phases, a hypersaline aqueous fluid and a low-salinity vapor-rich fluid. Boiling during cooling may have played an important role in metal precipitation. Pyrite δ34S values for the La Unión prospect range between 0.71‰ and 1.31‰, consistent with a homogeneous magmatic sulfur source. The fluids in equilibrium with the mineralized rocks have estimated δ18O values from 8‰ to 11.8‰, calculated for a temperature range of 480-505°C. The tectonic environment of the La Unión prospect, its high gold and low copper contents, the physical-chemical characteristics of the mineralizing fluids and the isotopic signature of the alteration minerals and fluids indicate that the La Unión gold mineralization is similar to the porphyry gold type, even though the ore

Hollow Au@Pd and Au@Pt core-shell nanoparticles as electrocatalysts for ethanol oxidation reactions

KAUST Repository

Song, Hyon Min

2012-09-27

Hybrid alloys among gold, palladium and platinum become a new category of catalysts primarily due to their enhanced catalytic effects. Enhancement means not only their effectiveness, but also their uniqueness as catalysts for the reactions that individual metals may not catalyze. Here, preparation of hollow Au@Pd and Au@Pt core-shell nanoparticles (NPs) and their use as electrocatalysts are reported. Galvanic displacement with Ag NPs is used to obtain hollow NPs, and higher reduction potential of Au compared to Ag, Pd, and Pt helps to produce hollow Au cores first, followed by Pd or Pt shell growth. Continuous and highly crystalline shell growth was observed in Au@Pd core-shell NPs, but the sporadic and porous-like structure was observed in Au@Pt core-shell NPs. Along with hollow core-shell NPs, hollow porous Pt and hollow Au NPs are also prepared from Ag seed NPs. Twin boundaries which are typically observed in large size (>20 nm) Au NPs were not observed in hollow Au NPs. This absence is believed to be due to the role of the hollows, which significantly reduce the strain energy of edges where the two lattice planes meet. In ethanol oxidation reactions in alkaline medium, hollow Au@Pd core-shell NPs show highest current density in forward scan. Hollow Au@Pt core-shell NPs maintain better catalytic activities than metallic Pt, which is thought to be due to the better crystallinity of Pt shells as well as the alloy effect of Au cores. © 2012 The Royal Society of Chemistry.

Comparison between the fragmentation processes in central Pb + Ag and Pb + Au collisions

International Nuclear Information System (INIS)

Jouault, B.; Royer, G.; Sebille, F.; Haddad, F.; Lecolley, J.F.

1996-01-01

The fragmentation processes of a medium mass system and of a very massive one formed in central collisions are compared within the Landau-Vlasov model taking into account both the isospin dependence and the two-body residual interactions. The simulations predict the formation of a roughly ellipsoidal source in the central Pb + Ag reactions while, for the Pb + Au system, the fragmentation occurs from an hollow source, the configuration of which being intermediate between bubble-like and toroidal shapes. This difference shapes explain and allow to reproduce semi-quantitatively the two different profiles of the experimental kinetic energy spectra. (authors)

Ag on Si(111) from basic science to application

Energy Technology Data Exchange (ETDEWEB)

Belianinov, Aleksey [Iowa State Univ., Ames, IA (United States)

2012-01-01

In our work we revisit Ag and Au adsorbates on Si(111)-7x7, as well as experiment with a ternary system of Pentacene, Ag and Si(111). Of particular interest to us is the Si(111)-(√3x√3)R30°}–Ag (Ag-Si-√3 hereafter). In this thesis I systematically explore effects of Ag deposition on the Ag-Si-√3 at different temperatures, film thicknesses and deposition fluxes. The generated insight of the Ag system on the Si(111) is then applied to generate novel methods of nanostructuring and nanowire growth. I then extend our expertise to the Au system on the Ag-Si(111) to gain insight into Au-Si eutectic silicide formation. Finally we explore behavior and growth modes of an organic molecule on the Ag-Si interface.

Mass and velocity of fragments from the reaction 17-115 MeV/u 40Ar + Cu, Ag and Au

International Nuclear Information System (INIS)

Colin, E.; Guinet, D.; Stern, M.

1998-01-01

Measurements are reported for fragment masses and velocities from the reactions 17-115 MeV/u 40 Ar + Cu, Ag and Au. High momentum and energy deposition are reported for selected events, even for higher incident energy. Further study is needed to understand their origin. (authors)

Quantum tunneling in real space: Tautomerization of single porphycene molecules on the (111) surface of Cu, Ag, and Au

Science.gov (United States)

Kumagai, Takashi; Ladenthin, Janina N.; Litman, Yair; Rossi, Mariana; Grill, Leonhard; Gawinkowski, Sylwester; Waluk, Jacek; Persson, Mats

2018-03-01

Tautomerization in single porphycene molecules is investigated on Cu(111), Ag(111), and Au(111) surfaces by a combination of low-temperature scanning tunneling microscopy (STM) experiments and density functional theory (DFT) calculations. It is revealed that the trans configuration is the thermodynamically stable form of porphycene on Cu(111) and Ag(111), whereas the cis configuration occurs as a meta-stable form. The trans → cis or cis → trans conversion on Cu(111) can be induced in an unidirectional fashion by injecting tunneling electrons from the STM tip or heating the surface, respectively. We find that the cis ↔ cis tautomerization on Cu(111) occurs spontaneously via tunneling, verified by the negligible temperature dependence of the tautomerization rate below ˜23 K. Van der Waals corrected DFT calculations are used to characterize the adsorption structures of porphycene and to map the potential energy surface of the tautomerization on Cu(111). The calculated barriers are too high to be thermally overcome at cryogenic temperatures used in the experiment and zero-point energy corrections do not change this picture, leaving tunneling as the most likely mechanism. On Ag(111), the reversible trans ↔ cis conversion occurs spontaneously at 5 K and the cis ↔ cis tautomerization rate is much higher than on Cu(111), indicating a significantly smaller tautomerization barrier on Ag(111) due to the weaker interaction between porphycene and the surface compared to Cu(111). Additionally, the STM experiments and DFT calculations reveal that tautomerization on Cu(111) and Ag(111) occurs with migration of porphycene along the surface; thus, the translational motion couples with the tautomerization coordinate. On the other hand, the trans and cis configurations are not discernible in the STM image and no tautomerization is observed for porphycene on Au(111). The weak interaction of porphycene with Au(111) is closest to the gas-phase limit and therefore the absence

Structure reactivity relationships during N2O hydrogenation over Au-Ag alloys: A study by field emission techniques

Science.gov (United States)

Jacobs, Luc; Barroo, Cédric; Gilis, Natalia; Lambeets, Sten V.; Genty, Eric; Visart de Bocarmé, Thierry

2018-03-01

To make available atomic oxygen at the surface of a catalyst is the key step for oxidation reactions on Au-based catalysts. In this context, Au-Ag alloys catalysts exhibit promising properties for selective oxidation reactions of alcohols: low temperature activity and high selectivity. The presence of O(ads) and its effects on the catalytic reactivity is studied via the N2O dissociative adsorption and subsequent hydrogenation. Field emission techniques are particularly suited to study this reaction: Field Ion Microscopy (FIM) and Field Emission Microscopy (FEM) enable to image the extremity of sharp metallic tips, the size and morphology of which are close to those of one single catalytic particle. The reaction dynamics is studied in the 300-320 K temperature range and at a pressure of 3.5 × 10-3 Pa. The main results are a strong structure/reactivity relationship during N2O + H2 reaction over Au-8.8 at.%Ag model catalysts. Comparison of high-resolution FIM images of the clean sample and FEM images during reaction shows a sensitivity of the reaction to the local structure of the facets, independently of the used partial pressures of both N2O and H2. This suggests a localised dissociative adsorption step for N2O and H2 with the formation of a reactive interface around the {210} facets.

Origin and evolution of mineralizing fluids and exploration of the Cerro Quema Au-Cu deposit (Azuero Peninsula, Panama) from a fluid inclusion and stable isotope perspective

Science.gov (United States)

Corral, Isaac; Cardellach, Esteve; Corbella, Merce; Canals, Angels; Griera, Albert; Gomez-Gras, David; Johnson, Craig A.

2017-01-01

Cerro Quema is a high sulfidation epithermal Au-Cu deposit with a measured, indicated and inferred resource of 35.98 Mt. @ 0.77 g/t Au containing 893,600 oz. Au (including 183,930 oz. Au equiv. of Cu ore). It is characterized by a large hydrothermal alteration zone which is interpreted to represent the lithocap of a porphyry system. The innermost zone of the lithocap is constituted by vuggy quartz with advanced argillic alteration locally developed on its margin, enclosed by a well-developed zone of argillic alteration, grading to an external halo of propylitic alteration. The mineralization occurs in the form of disseminations and microveinlets of pyrite, chalcopyrite, enargite, tennantite, and trace sphalerite, crosscut by quartz, barite, pyrite, chalcopyrite, sphalerite and galena veins.Microthermometric analyses of two phase (L + V) secondary fluid inclusions in igneous quartz phenocrysts in vuggy quartz and advanced argillically altered samples indicate low temperature (140–216 °C) and low salinity (0.5–4.8 wt% NaCl eq.) fluids, with hotter and more saline fluids identified in the east half of the deposit (Cerro Quema area).Stable isotope analyses (S, O, H) were performed on mineralization and alteration minerals, including pyrite, chalcopyrite, enargite, alunite, barite, kaolinite, dickite and vuggy quartz. The range of δ34S of sulfides is from − 4.8 to − 12.7‰, whereas δ34S of sulfates range from 14.1 to 17.4‰. The estimated δ34SΣS of the hydrothermal fluid is − 0.5‰. Within the advanced argillic altered zone the δ34S values of sulfides and sulfates are interpreted to reflect isotopic equilibrium at temperatures of ~ 240 °C. The δ18O values of vuggy quartz range from 9.0 to 17.5‰, and the δ18O values estimated for the vuggy quartz-forming fluid range from − 2.3 to 3.0‰, indicating that it precipitated from mixing of magmatic fluids with surficial fluids. The δ18O of kaolinite ranges from 12.7 to 18.1‰ and �

Method and apparatus for epithermal neutron porosity well logging

International Nuclear Information System (INIS)

Hertzog, R.C.; Loomis, W.A.; Wraight, P.

1991-01-01

This patent describes a method for investigating the porosity of a subsurface earth formation surrounding a borehole. It comprises repetitively irradiating the borehole and earth formation with discrete bursts of high energy neutrons from a neutron source, which neutrons interact with nuclei of the materials in the borehole and the formation to produce therein populations of epithermal neutrons; detecting the populations of epithermal neutrons at near and far locations in the borehole spaced apart longitudinally by different distances from the neutron source; generating count signals indicative of the magnitudes of the detected epithermal neutron populations at the respective near and far locations; detecting the decay of the epithermal neutron populations following the neutron bursts at least at one location in the borehole and generating signals representative thereof; deriving from the decay signals a signal indicative of the slowing down time of epithermal neutrons in the formation of the at least one location; and deriving from the near and far count signals and the slowing down time signal a measurement signal representative of the porosity of the formation surrounding the borehole inherently compensated for the effects of tool standoff on the responses of the logging tool

Temporal and spatial distribution of alteration, mineralization and fluid inclusions in the transitional high-sulfidation epithermal-porphyry copper system at Red Mountain, Arizona

Science.gov (United States)

Lecumberri-Sanchez, Pilar; Newton, M. Claiborne; Westman, Erik C.; Kamilli, Robert J.; Canby, Vertrees M.; Bodnar, Robert J.

2013-01-01

Red Mountain, Arizona, is a Laramide porphyry Cu system (PCD) that has experienced only a modest level of erosion compared to most other similar deposits in the southwestern United States. As a result, the upper portion of the magmatic–hydrothermal system, which represents the transition from shallower high-sulfidation epithermal mineralization to deeper porphyry Cu mineralization, is well preserved. Within the Red Mountain system, alteration, mineralization and fluid inclusion assemblages show a systematic distribution in both time and space. Early-potassic alteration (characterized by the minerals biotite and magnetite) is paragenetically earlier than late-potassic alteration (K-feldspar–anhydrite) and both are followed by later phyllic (sericite–pyrite) alteration. Advanced argillic alteration (pyrophyllite–alunite–other clay minerals) is thought to be coeval with or postdate phyllic alteration. Minerals characteristic of advanced argillic alteration are present in the near surface. Phyllic alteration extends to greater depths compared to advanced argillic alteration. Early-potassic and late-potassic alteration are only observed in the deepest part of the system. Considerable overlap of phyllic alteration with both early-potassic and late-potassic alteration zones is observed. The hypogene mineralization contains 0.4–1.2% Cu and is spatially and temporally related to the late-potassic alteration event. Molybdenum concentration is typically In the deepest part of the system, an early generation of low-to-moderate density and salinity liquid + vapor inclusions with opaque daughter minerals is followed in time by halite-bearing inclusions that also contain opaque daughter minerals indicating that an early intermediate-density magmatic fluid evolved to a high-density, high-salinity mineralizing fluid. The increase in density and salinity of fluids with time observed in the deeper parts of the system may be the result of immiscibility (“boiling”) of

Design of filtered epithermal neutron beams for BNC

International Nuclear Information System (INIS)

Greenwood, R.C.

1986-01-01

The design principles of filters (installed in nuclear reactors) to provide epithermal neutron beams suitable for use in 10 B Neutron Capture Therapy (BNCT) are reviewed. The goal of such filters is to provide epithermal neutron beams within an energy range of 1 keV to 30 keV with fluxes in excess of 5 x 10 8 neutrons/cm 2 .s, and having acceptably low contaminant fast neutron (> 30 keV) and gamma components. Filters considered for this application include 238 U, Sc, Fe/Al and Al/S. It is shown that in order to achieve a goal epithermal neutron flux of > 5 x 10 8 neutrons/cm 2 .s, such filters must be located in radial beam channels which view essentially the complete reactor core. Based on considerations of estimated epithermal fluxes, cost and availability of materials, and transmitted neutron energy spectrum, it is suggested that a filter consisting of elements of Al, S, Ti and V might prove to be an optimum design for BNCT applications. 13 references, 3 figures, 8 tables

Anomolous, intensity dependent losses in Au(32+) beams

International Nuclear Information System (INIS)

Blaskiewicz, M.; Ahrens, L.; Calvani, H.

1997-01-01

The AGS Booster is a rapid cycling proton and heavy ion synchrotron. Anomolous, intensity dependent losses in Au(32+) beams have been observed in the AGS Booster. No collective signal is expected, or observed, but increasing the number of injected ions decreases the beam lifetime. The loss rates for Au(32+) are compared with those for Au(15+)

Hyperspectral remote sensing applied to mineral exploration in southern Peru: A multiple data integration approach in the Chapi Chiara gold prospect

Science.gov (United States)

Carrino, Thais Andressa; Crósta, Alvaro Penteado; Toledo, Catarina Labouré Bemfica; Silva, Adalene Moreira

2018-02-01

Remote sensing is a strategic key tool for mineral exploration, due to its capacity of detecting hydrothermal alteration minerals or alteration mineral zones associated with different types of mineralization systems. A case study of an epithermal system located in southern Peru is presented, aimed at the characterization of mineral assemblies for discriminating potential high sulfidation epithermal targets, using hyperspectral imagery integrated with petrography, XRD and magnetic data. HyMap images were processed using the Mixture Tuned Matched Filtering (MTMF) technique for producing alteration map in the Chapi Chiara epithermal gold prospect. Extensive areas marked by advanced argillic alteration (alunite-kaolinite-dickite ± topaz) were mapped in detail, as well as limited argillic (illite-smectite) and propylitic (chlorite spectral domain) alteration. The magmatic-hydrothermal processes responsible for the formation of hypogene minerals were also related to the destruction of ferrimagnetic minerals (e.g., magnetite) of host rocks such as andesite, and the remobilization/formation of paramagnetic Fe-Ti oxides (e.g., rutile, anatase). The large alteration zones of advanced argillic alteration are controlled by structures related to a regional NW-SE trend, and also by local NE-SW and ENE-WSW ones.

A comparative study of Cu, Ag and Au doped CeO_2 in the total oxidation of volatile organic compounds (VOCs)

International Nuclear Information System (INIS)

Aboukaïs, Antoine; Skaf, Mira; Hany, Sara; Cousin, Renaud; Aouad, Samer; Labaki, Madona; Abi-Aad, Edmond

2016-01-01

Total oxidation of two Volatile Organic Compounds (VOCs), propylene and toluene, was investigated over M/CeO_2 catalysts, where M is a metal from IB group (i.e. Au, Ag, Cu), prepared by two different methods: the conventional wet impregnation and the deposition-precipitation. The catalysts have been characterized by means of total surface area (BET), X-ray diffraction (XRD), electron paramagnetic resonance (EPR), X-ray photoelectron spectroscopy (XPS), diffuse reflectance ultra-violet-visible spectroscopy (DR-UV/Vis), and temperature-programmed reduction (TPR), in order to explain the differences observed in their catalytic activity towards the studied reactions. By comparing the two different preparation methods, the presence of metal in high oxidation state for gold and silver, and the presence of clusters for copper were the main factors responsible for the high catalytic activity. This latter was also found to be related, when comparing the different IB metals, to the values of the oxidation/reduction potential of the redox couples of the different metals. - Highlights: • IB metals (Au, Ag and Cu) were supported on ceria (CeO_2) by two different methods. • The solids were tested as catalysts for total oxidation of propylene and toluene. • The deposition-precipitation is better for Au whereas for Ag and Cu it is the impregnation. • High oxidation states of gold and silver and clusters of copper enhanced catalytic behavior. • Catalytic activity is linked to the oxidation/reduction potential of the redox IB couples.

Design and Investigation of SST/nc-Si:H/M (M = Ag, Au, Ni and M/nc-Si:H/M Multifunctional Devices

Directory of Open Access Journals (Sweden)

A. F. Qasrawi

2013-01-01

Full Text Available Hydrogenated nanocrystalline Silicon thin films prepared by the very high frequency chemical vapor deposition technique (VHF-CVD on stainless steel (SST substrates are used to design Schottky point contact barriers for the purpose of solar energy conversion and passive electronic component applications. In this process, the contact performance between SST and M (M = Ag, Au, and Ni and between Ag, Au, and Ni electrodes was characterized by means of current-voltage, capacitance-voltage, and light intensity dependence of short circuit ( current and open circuit voltage ( of the contacts. Particularly, the devices ideality factors, barrier heights were evaluated by the Schottky method and compared to the Cheung's. Best Schottky device performance with lowest ideality factor suitable for electronic applications was observed in the SST/nc-Si:H/Ag structure. This device reflects a of 229 mV with an of 1.6 mA/cm2 under an illumination intensity of ~40 klux. On the other hand, the highest being 9.0 mA/cm2 and the of 53.1 mV were observed for Ni/nc-Si:H/Au structure. As these voltages represent the maximum biasing voltage for some of the designed devices, the SST/nc-Si:H/M and M/nc-Si:H/M can be regarded as multifunctional self-energy that provided electronic devices suitable for active or passive applications.

Temperature imaging using epithermal neutrons

International Nuclear Information System (INIS)

Fowler, P.H.; Taylor, A.D.

1987-08-01

The paper concerns the temperature measurement of suitable targets, both remotely and non-invasively, using epithermal neutrons. The text was presented at the Neutron Resonance Radiography Workshop, Los Alamos, U.S.A., 1987. The technique is demonstrated for tantalum foils at different temperatures, using a pulsed beam of epithermal neutrons, at both Los Alamos and ISIS (United Kingdom). Results on the measured time-of-flight spectra and the tantalum resonances are presented. Beam properties and fluxes at ISIS are discussed. Features of the proposed detectors suitable for the temperature technique are outlined, along with the data analysis, the moving targets, the cyclic temperature variations and transients, and the usefulness of the technique. (U.K.)

A wide range optical pH sensor for living cells using Au@Ag nanoparticles functionalized carbon nanotubes based on SERS signals.

Science.gov (United States)

Chen, Peng; Wang, Zhuyuan; Zong, Shenfei; Chen, Hui; Zhu, Dan; Zhong, Yuan; Cui, Yiping

2014-10-01

p-Aminothiophenol (pATP) functionalized multi-walled carbon nanotubes (MWCNTs) have been demonstrated as an efficient pH sensor for living cells. The proposed sensor employs gold/silver core-shell nanoparticles (Au@Ag NPs) functionalized MWCNTs hybrid structure as the surface-enhanced Raman scattering (SERS) substrate and pATP molecules as the SERS reporters, which possess a pH-dependent SERS performance. By using MWCNTs as the substrate to be in a state of aggregation, the pH sensing range could be extended to pH 3.0∼14.0, which is much wider than that using unaggregated Au@Ag NPs without MWCNTs. Furthermore, the pH-sensitive performance was well retained in living cells with a low cytotoxicity. The developed SERS-active MWCNTs-based nanocomposite is expected to be an efficient intracellular pH sensor for bio-applications.

3He induced reactions on natAg and 197Au at 1.8, 3.6 and 4.8 GeV

International Nuclear Information System (INIS)

Brzychczyk, J.; Jagiellonian Univ., Krakow; Pollacco, E.C.; Volant, C.; Legrain, R.; Kwiatkowski, K.; Morley, K.B.; Renshaw-Foxford, E.; Bracken, D.S.; Viola, V.E.; Yoder, N.R.

1995-03-01

The 3 He induced reactions on Ag and Au are studied using a large solid angle and low energy threshold detector array. The data show consistency with intranuclear cascade and expanding emitting source description. Charge moment analysis is presented. (author). 18 refs., 8 figs