Set potential regulation reveals additional oxidation peaks of Geobacter sulfurreducens anodic biofilms

KAUST Repository

Zhu, Xiuping; Yates, Matthew D.; Logan, Bruce E.

2012-01-01

larger range of set potentials was used to acclimate electroactive biofilms. The potentials of oxidation peaks obtained with G. sulfurreducens biofilms acclimated at 0.60 V (vs. Ag/AgCl) were different from those that developed at - 0.46 V, and both

Large short-baseline νμ disappearance

International Nuclear Information System (INIS)

Giunti, Carlo; Laveder, Marco

2011-01-01

We analyze the LSND, KARMEN, and MiniBooNE data on short-baseline ν μ →ν e oscillations and the data on short-baseline ν e disappearance obtained in the Bugey-3 and CHOOZ reactor experiments in the framework of 3+1 antineutrino mixing, taking into account the MINOS observation of long-baseline ν μ disappearance and the KamLAND observation of very-long-baseline ν e disappearance. We show that the fit of the data implies that the short-baseline disappearance of ν μ is relatively large. We obtain a prediction of an effective amplitude sin 2 2θ μμ > or approx. 0.1 for short-baseline ν μ disappearance generated by 0.2 2 2 , which could be measured in future experiments.

Set potential regulation reveals additional oxidation peaks of Geobacter sulfurreducens anodic biofilms

KAUST Repository

Zhu, Xiuping

2012-08-01

Higher current densities produced in microbial fuel cells and other bioelectrochemical systems are associated with the presence of various Geobacter species. A number of electron transfer components are involved in extracellular electron transfer by the model exoelectrogen, Geobacter sulfurreducens. It has previously been shown that 5 main oxidation peaks can be identified in cyclic voltammetry scans. It is shown here that 7 separate oxidation peaks emerged over relatively long periods of time when a larger range of set potentials was used to acclimate electroactive biofilms. The potentials of oxidation peaks obtained with G. sulfurreducens biofilms acclimated at 0.60 V (vs. Ag/AgCl) were different from those that developed at - 0.46 V, and both of their peaks were different from those obtained for biofilms incubated at - 0.30 V, 0 V, and 0.30 V. These results expand the known range of potentials for which G. sulfurreducens produces identifiable oxidation peaks that could be important for extracellular electron transfer. © 2012 Elsevier B.V.

Reducing strength prevailing at root surface of plants promotes reduction of Ag+ and generation of Ag(0/Ag2O nanoparticles exogenously in aqueous phase.

Directory of Open Access Journals (Sweden)

Peddisetty Pardha-Saradhi

Full Text Available Potential of root system of plants from wide range of families to effectively reduce membrane impermeable ferricyanide to ferrocyanide and blue coloured 2,6-dichlorophenol indophenol (DCPIP to colourless DCPIPH2 both under non-sterile and sterile conditions, revealed prevalence of immense reducing strength at root surface. As generation of silver nanoparticles (NPs from Ag+ involves reduction, present investigations were carried to evaluate if reducing strength prevailing at surface of root system can be exploited for reduction of Ag+ and exogenous generation of silver-NPs. Root system of intact plants of 16 species from 11 diverse families of angiosperms turned clear colorless AgNO3 solutions, turbid brown. Absorption spectra of these turbid brown solutions showed silver-NPs specific surface plasmon resonance peak. Transmission electron microscope coupled with energy dispersive X-ray confirmed the presence of distinct NPs in the range of 5-50 nm containing Ag. Selected area electron diffraction and powder X-ray diffraction patterns of the silver NPs showed Bragg reflections, characteristic of crystalline face-centered cubic structure of Ag(0 and cubic structure of Ag2O. Root system of intact plants raised under sterile conditions also generated Ag(0/Ag2O-NPs under strict sterile conditions in a manner similar to that recorded under non-sterile conditions. This revealed the inbuilt potential of root system to generate Ag(0/Ag2O-NPs independent of any microorganism. Roots of intact plants reduced triphenyltetrazolium to triphenylformazon and impermeable ferricyanide to ferrocyanide, suggesting involvement of plasma membrane bound dehydrogenases in reduction of Ag+ and formation of Ag(0/Ag2O-NPs. Root enzyme extract reduced triphenyltetrazolium to triphenylformazon and Ag+ to Ag(0 in presence of NADH, clearly establishing potential of dehydrogenases to reduce Ag+ to Ag(0, which generate Ag(0/Ag2O-NPs. Findings presented in this manuscript put

Huge residual resistivity in the quantum critical region of CeAgSb2

International Nuclear Information System (INIS)

Nakashima, Miho; Kirita, Shingo; Asai, Rihito; Kobayashi, Tatsuo C; Okubo, Tomoyuki; Yamada, Mineko; Thamizhavel, Arumugam; Inada, Yoshihiko; Settai, Rikio; Galatanu, Andre; Yamamoto, Etsuji; Ebihara, Takao; Onuki, Yoshichika

2003-01-01

We have studied the effect of pressure on the electrical resistivity of a high-quality single crystal CeAgSb 2 which has a small net ferromagnetic moment of 0.4μ B /Ce. The magnetic ordering temperature T ord = 9.7 K decreases with increasing pressure p and disappears at a critical pressure p c ≅ 3.3 GPa. The residual resistivity, which is close to zero up to 3 GPa, increases steeply above 3 GPa, reaching 55μΩ cm at p c . A huge residual resistivity is found to appear when the magnetic order disappears. (letter to the editor)

Positron annihilation studies of vacancies in Ag-Zn alloys

International Nuclear Information System (INIS)

Chabik, S.

1982-01-01

The temperature dependence of annihilation rate, F(T), at the peak of angular correlation curve has been measured for Ag-29.2%at Zn and Ag-50%at Zn alloys. By applying the trapping model the vacancy formation energy for Ag-29.2%at Zn alloy has been found to be equal to 0.94+-0.06 eV. It has been found that the course of the F(T) curve for Ag-50%at Zn depends on the phase composition and thermal history of the investigated sample. For alloys containing not more than 50%at Zn, the concentration dependence of the vacancy formation energy for Ag-Zn alloys is very similar to that for Cu-Zn alloys. (Auth.)

Antibacterial properties of Ag-exchanged Philippine natural zeolite-chitosan composites

Science.gov (United States)

Taaca, Kathrina Lois M.; Olegario, Eleanor M.; Vasquez, Magdaleno R.

2017-12-01

Zeolites are microporous minerals composed of silicon, aluminum and oxygen. These aluminosilicates consist of tetrahedral units which produce open framework structures to generate a system of pores and cavities of molecular dimensions. Zeolites are naturally abundant and can be mined in most parts of the world. In this study, natural zeolites (NaZ) which are locally-sourced here in the Philippines were investigated to determine its properties. An ion-exchange process was utilized, using the zeolite to silver (Ag) solution ratio of 1:20 (w/v), to incorporate Ag into the zeolite framework. Characterizations such as XRD, AAS, and Agar diffusion assay were used to evaluate the properties of the synthesized Ag-exchanged zeolites (AgZ). X-ray diffraction revealed that both NaZ and AgZ have peaks mostly corresponding to the clinoptilolite structure, with some trace peaks of the mordenite and quartz. Absorption spectroscopy revealed that the ion exchange process added about 0.61188g of silver into the zeolite structure. This Ag content was seen to be enough to make the AgZ sample exhibit an antibacterial effect where clearing zones against E. coli and S. aureus were observed in the agar diffusion assay, respectively. The AgZ sample was also tested as ceramic filler to a polymer matrix-chitosan. The diffusion assay revealed presence of antibacterial activity to the polymer composite with AgZ fillers. These results indicate that the Philippine natural zeolite, incorporated with metals such as Ag, can be used as an antibacterial agent and can be developed as a ceramic filler to improve the antibacterial property of composite materials for biomedical application.

MIS-11 duration key to disappearance of the Greenland ice sheet

Science.gov (United States)

Robinson, Alexander; Alvarez-Solas, Jorge; Calov, Reinhard; Ganopolski, Andrey; Montoya, Marisa

2017-07-01

Palaeo data suggest that Greenland must have been largely ice free during Marine Isotope Stage 11 (MIS-11). However, regional summer insolation anomalies were modest during this time compared to MIS-5e, when the Greenland ice sheet likely lost less volume. Thus it remains unclear how such conditions led to an almost complete disappearance of the ice sheet. Here we use transient climate-ice sheet simulations to simultaneously constrain estimates of regional temperature anomalies and Greenland's contribution to the MIS-11 sea-level highstand. We find that Greenland contributed 6.1 m (3.9-7.0 m, 95% credible interval) to sea level, ~7 kyr after the peak in regional summer temperature anomalies of 2.8 °C (2.1-3.4 °C). The moderate warming produced a mean rate of mass loss in sea-level equivalent of only around 0.4 m per kyr, which means the long duration of MIS-11 interglacial conditions around Greenland was a necessary condition for the ice sheet to disappear almost completely.

Preparation of AgBr Nanoparticles in Microemulsions Via Reaction of AgNO3 with CTAB Counterion

International Nuclear Information System (INIS)

Husein, Maen M.; Rodil, Eva; Vera, Juan H.

2007-01-01

Nanoparticles of AgBr were prepared by precipitating AgBr in the water pools of microemulsions consisting of CTAB, n-butanol, isooctane and water. An aqueous solution of AgNO 3 added to the microemulsion was the source of Ag + ions. The formation of AgBr nanoparticles in microemulsions through direct reaction with the surfactant counterion is a novel approach aimed at decreasing the role of intermicellar nucleation on nanoparticle formation for rapid reactions. The availability of the surfactant counterion in every reverse micelle and the rapidity of the reaction with the counterion trigger nucleation within individual reverse micelles. The effect of the following variables on the particle size and size distribution was investigated: the surfactant and cosurfactant concentrations, moles of AgNO 3 added, and water to surfactant mole ratio, R. High concentration of the surfactant or cosurfactant, or high water content of the microemulsion favored intermicellar nucleation and resulted in the formation of large particles with broad size distribution, while high amounts of AgNO 3 favored nucleation within individual micelles and resulted in small nanoparticles with narrow size distribution. A blue shift in the UV absorption threshold corresponding to a decrease in the particle size was generally observed. Notably, the variation of the absorption peak size with the nanoparticle size was opposite to those reported by us in previous studies using different surfactants

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

Synthesis and antimicrobial evaluation of nanostructures ZrO2:AG against staphylococcus aureus by hydrothermal method

Energy Technology Data Exchange (ETDEWEB)

Nova, C.V.; Reis, K.H.; Galico, D.A.; Venturini, J.; Pontes, F.M.L.; Pinheiro, A.L. [Universidade Estadual Paulista Julio de Mesquita Filho (UNESP), SP (Brazil); Longo, E. [Universidade Estadual de Campinas (UNICAMP), SP (Brazil)

2016-07-01

Nanostructures of zirconia (ZrO2) has shown great prominence in the area of advanced materials and shows excellent properties such as chemical stability, mechanical strength, electrical and optical properties. When certain metals are supported on the compound, such as Fe, Ag, Au and Al, a potentiation of some properties, such as bactericide and fungicide can occur. Thus, this work deals with the synthesis and characterization of ZrO2 and ZrO2:Ag (1% and 10 % of Ag) nanostructures and the study of the influence of the antimicrobial activity against Staphylococcus aureus. X-ray powder diffractograms of the zirconia and silver with zirconia shown the formation of well defined peaks of tetragonal zirconia in all the samples. Although the ZrO2:Ag (10 % of Ag) shown the characteristics peaks of cubic silver, these peaks do not appear in ZrO2:Ag (1 % of Ag) due to the small amount of silver in comparison with zirconium. The crystal size was estimated by the Scherrer equation and the calculated values for zirconia were 12.84, 12.27 and 12.61 nm for ZrO2, ZrO2 : Ag (1%) and ZrO2 : Ag (10%) respectively and the silver crystal size was 8,09 nm. Diffuse reflectance of the silver particles shown a broad plasmon band at 405 and 424 nm for the ZrO2 : Ag (1%) and ZrO2 : Ag (10%). Antimicrobial assay demonstrated that ZrO2 showed a bacteriostatic effect (61 %) and the inclusion of the silver in the ZrO2 matrix enhanced this effect to 65-72 %. Both particles with different silver content shown similar effect {[ZrO2:Ag 1%] = [ZrO2:Ag 10%]>[ZrO2]}.(author)

Disappearance and disintegration of comets

Science.gov (United States)

Sekanina, Z.

1984-01-01

The present investigation has the objective to provide a summary of the existing evidence on the disappearance of comets and to draw conclusions regarding the physical processes involved in the disappearance. Information concerning the classification of evidence and the causes of apparent disappearance of comets is presented in a table. Attention is given to the dissipating comets, the headless sungrazing comet 1887 I, and the physical behavior of the dissipating comets and the related phenomena. It is found that all comets confined to the planetary region of the solar system decay on astronomically short time scales. However, only some of them appear to perish catastrophically. Some of the observed phenomena could be successfully interpreted. But little insight has been obtained into the character of the processes which the dissipating comets experience.

Plasma disappearance, urine excretion, and tissue distribution of ribavirin in rats and rhesus monkeys

International Nuclear Information System (INIS)

Ferrara, E.A.; Oishi, J.S.; Wannemacher, R.W. Jr.; Stephen, E.L.

1981-01-01

Ribavirin has been shown to have broad-spectrum antiviral. To study its tissue distribution and disappearance rate, a single dose of 10 mg/kg which contained 10 microCi of [14C]ribavirin was injected intravenously into rhesus monkeys and intramuscularly into monkeys and rats. Except for peak plasma concentrations and the initial phases of the plasma disappearance and urine excretion curves, no significant difference was observed between plasma, tissue, or urine values for intramuscularly or intravenously injected monkeys. Plasma disappearance curves were triphasic; plasma concentrations of ribavirin were similar for both monkeys and rats. Rats excreted ribavirin in the urine more rapidly and to a greater extent (82% excreted in 24 h) than did monkeys (60% excreted in 72 h). In the rat, only 3% of the injected [14C]ribavirin was detected in expired CO2. Therefore, for both species, urine was the major route for the elimination of labeled ribavirin and its metabolites from the body. In monkeys, the amount of parent drug in blood cells increased through 48 h and remained stable for 72 h, whereas in rats, ribavirin decreased at a rate similar to the plasma disappearance curve. Concentrations of ribavirin at 8 h were consistently higher in monkeys than in rats for all tissues except the brain. Thus, these differences in blood cellular components and organ content and in urine excretion suggested that there was greater tissue retention of ribavirin in monkeys than in rats

Atom beam sputtered Ag-TiO{sub 2} plasmonic nanocomposite thin films for photocatalytic applications

Energy Technology Data Exchange (ETDEWEB)

Singh, Jaspal; Sahu, Kavita [School of Basic and Applied Sciences, Guru Gobind Singh Indraprastha University, Dwarka, NewDelhi 110078 (India); Pandey, A. [Solid State Physics Laboratory, Defence Research and Development Organization, Timarpur, Delhi 110054 (India); Kumar, Mohit [Institute of Physics, Sachivalaya Marg, Bhubaneswar, Odisha 751005 (India); Ghosh, Tapas; Satpati, B. [Saha Institute of Nuclear Physics, HBNI, 1/AF, Bidhannagar, Kolkata 700064 (India); Som, T.; Varma, S. [Institute of Physics, Sachivalaya Marg, Bhubaneswar, Odisha 751005 (India); Avasthi, D.K. [Amity Institute of Nanotechnology, Noida 201313, Uttar Pradesh (India); Mohapatra, Satyabrata, E-mail: smiuac@gmail.com [School of Basic and Applied Sciences, Guru Gobind Singh Indraprastha University, Dwarka, NewDelhi 110078 (India)

2017-07-31

The development of nanocomposite coatings with highly enhanced photocatalytic activity is important for photocatalytic purification of water and air. We report on the synthesis of Ag-TiO{sub 2} nanocomposite thin films with highly enhanced photocatalytic activity by atom beam co-sputtering technique. The effects of Ag concentration on the structural, morphological, optical, plasmonic and photocatalytic properties of the nanocomposite thin films were investigated. UV–visible DRS studies revealed the presence of surface plasmon resonance (SPR) peak characteristic of Ag nanoparticles together with the excitonic absorption peak originating from TiO{sub 2} nanoparticles in the nanocomposites. XRD studies showed that the nanocomposite thin films consist of Ag nanoparticles and rutile TiO{sub 2} nanoparticles. The synthesized Ag-TiO{sub 2} nanocomposite thin films with 5 at% Ag were found to exhibit highly enhanced photocatalytic activity for sun light driven photocatalytic degradation of methylene blue in water, indicating their potential application in water purification.

Optically stimulated luminescence (OSL) from Ag-doped Li2B4O7 crystals

International Nuclear Information System (INIS)

Kananen, B.E.; Maniego, E.S.; Golden, E.M.; Giles, N.C.; McClory, J.W.; Adamiv, V.T.; Burak, Ya.V.; Halliburton, L.E.

2016-01-01

Optically stimulated luminescence (CW-OSL) is observed from Ag-doped lithium tetraborate (Li 2 B 4 O 7 ) crystals. Photoluminescence, optical absorption, and electron paramagnetic resonance (EPR) are used to identify the defects participating in the OSL process. As-grown crystals have Ag + ions substituting for Li + ions. They also have Ag + ions occupying interstitial sites. During a room-temperature exposure to ionizing radiation, holes are trapped at the Ag + ions that replace Li + ions and electrons are trapped at the interstitial Ag + ions, i.e., the radiation forms Ag 2+ (4d 9 ) ions and Ag 0 (4d 10 5s 1 ) atoms. These Ag 2+ and Ag 0 centers have characteristic EPR spectra. The Ag 0 centers also have a broad optical absorption band peaking near 370 nm. An OSL response is observed when the stimulation wavelength overlaps this absorption band. Specifically, stimulation with 400 nm light produces an intense OSL response when emission is monitored near 270 nm. Electrons optically released from the Ag 0 centers recombine with holes trapped at Ag 2+ ions to produce the ultraviolet emission. The OSL response is progressively smaller as the stimulation light is moved to longer wavelengths (i.e., away from the 370 nm peak of the absorption band of the Ag 0 electron traps). Oxygen vacancies are also present in the Ag-doped Li 2 B 4 O 7 crystals, and their role in the OSL process as a secondary relatively short-lived electron trap is described.

The optical and mechanical properties of PVA-Ag nanocomposite films

Energy Technology Data Exchange (ETDEWEB)

El-Shamy, A.G.; Attia, W.; Abd El-Kader, K.M., E-mail: kamalmarei@yahoo.com

2014-03-25

Highlights: • We prepared PVA -Ag composite films which used in different filed of applications. • The XRD results showed Ag nanoparticles entering the polymer PVA matrix. • Optical band gap as a result of doping has been found to be reduced significantly. • Young's modulus increases while the strain decreases due to increasing Ag content. -- Abstract: Poly (vinyl alcohol) (PVA) loaded silver (Ag) nanoparticles were successfully prepared by chemical reduction methods. The synthesized nanoparticles are characterized using UV–visible spectrophotometer, X-ray diffractometer (XRD) and Transmission electron microscope (TEM). The contents of the inorganic phase in the nanocomposites were determined by using atomic absorption spectroscopy (AA) for silver, and were found to be 0.2, 0.4, 0.8 and 1.5 wt.%. Optical absorption studies in the wavelength range 190–900 nm showed additional peak at 420 nm for differently doped films, in addition to the peak at 200 nm for undoped PVA film. There is observable change in the absorbed intensity at 420 nm with filling levels. This is due to the link between the Ag metal ion and the polymer OH- groups. The indirect energy gaps were calculated. It was found that Young’s modulus and the strength at the break increase, while the energy gaps and the strain decrease as the concentration of Ag content is increased. The XRD results showed that the Ag nanoparticles entering the polymer PVA matrix and the crystallinity was strongly influenced by the amount of Ag nanoparticles. The electron diffraction image for the highest concentration sample shows the crystalline nature of the silver metal nanoparticles. TEM of the nanocomposite films revealed the presence of Ag particles with average diameter of 12 nm.

Structure and photoluminescence properties of Ag-coated ZnO nano-needles

Energy Technology Data Exchange (ETDEWEB)

Li Xiaozhu, E-mail: Lixiaozhu1019@21cn.com [Department of Physics, Shaoguan University, Shaoguan, Guangdong 512005 (China) and Department of Physics and Key Laboratory of Acoustic and Photonic Materials and Devices of Ministry of Education, Wuhan University, Wuhan, Hubei 430072 (China); Wang Yongqian [Engineering Research Center of Nano-Geomaterials of Ministry of Education (China University of Geosciences), Wuhan, Hubei 430074 (China)

2011-05-12

Highlights: > ZnO nano-needles were synthesized by thermal oxidation. > Their surfaces were coated with Ag by pulse electro-deposition technique. > The uncoated and coated ZnO nano-needles were characterized. > The results showed that the prepared ZnO nano-needles have been coated with Ag successfully. > The photoluminescence spectrums of ZnO nano-needles with Ag-coated and uncoated were analyzed, finding that the Ag-coated ZnO nano-needles can increase the absorption of UV light. - Abstract: A large number of zinc oxide (ZnO) nano-needles were synthesized by thermal oxidation of pure zinc. The surfaces of ZnO nano-needles were coated with a layer of Ag by pulse electro-deposition technique. The uncoated and coated ZnO nano-needles were characterized by using the X-ray diffraction and the scanning electron microscope (SEM). The results showed that the uncoated samples were close-packed hexagonal structure, which showed needle-like morphology. Their average diameter is about 40 nm, lengths up to 5 {mu}m. At the same time we observed that the prepared ZnO nano-needles have been coated with Ag successfully. The photoluminescence spectrums of ZnO nano-needles with Ag-coated and uncoated were analyzed, finding that the uncoated ZnO nano-needles have two fluorescence peaks at 388 nm and 470.8 nm, respectively, the relative intensity of 143.4 and 93.61; and the Ag-coated ZnO nano-needles showed a pair of strong peaks at 387.4 nm and 405.2 nm, the relative intensity of 1366 and 1305, respectively, indicating that the Ag-coated ZnO nano-needles can increase the absorption of UV light.

Extracellular electron transfer mechanism in Shewanella loihica PV-4 biofilms formed at indium tin oxide and graphite electrodes

Digital Repository Service at National Institute of Oceanography (India)

Jain, A.; Connolly, J.O.; Woolley, R.; Krishnamurthy, S.; Marsili, E.

/electrode interface [21]. After 24 h from inoculation, the sigmoidal wave disappeared and cyclic voltammetry detected reversible peaks with Em value -0.3 V, most likely due to the production of redox mediator(s) in the cell suspension under anaerobic conditions... reported earlier from the whole cell voltammetry of S. loihica PV- 4 (-0.054 V vs. Ag/AgCl) [18] as well as of S. oneidensis MR-1 (-0.07 V vs. Ag/AgCl) [29]. The Em value obtained for RC (I) was shifted to a more positive potential from those reported...

Recombination luminescence of Cu and/or Ag doped lithium tetraborate single crystals

Energy Technology Data Exchange (ETDEWEB)

Romet, I. [Institute of Physics, University of Tartu, W. Ostwaldi Str. 1, 50411 Tartu (Estonia); Aleksanyan, E. [Institute of Physics, University of Tartu, W. Ostwaldi Str. 1, 50411 Tartu (Estonia); A. Alikhanyan National Science Laboratory, 2 Br. Alikhanyan Str., 0036 Yerevan (Armenia); Brik, M.G. [Institute of Physics, University of Tartu, W. Ostwaldi Str. 1, 50411 Tartu (Estonia); College of Sciences, Chongqing University of Posts and Telecommunications, 400065 Chongqing (China); Institute of Physics, Jan Dlugosz University, Armii Krajowej 13/15, PL-42200 Czestochowa (Poland); Corradi, G. [Institute for Solid State Physics and Optics, Wigner Research Centre for Physics, Hungarian Academy of Sciences, Konkoly-Thege M. út 29-33, H-1121 Budapest (Hungary); Kotlov, A. [Photon Science at DESY, Notkestrasse 85, 22607 Hamburg (Germany); Nagirnyi, V., E-mail: vitali.nagirnoi@ut.ee [Institute of Physics, University of Tartu, W. Ostwaldi Str. 1, 50411 Tartu (Estonia); Polgár, K. [Institute for Solid State Physics and Optics, Wigner Research Centre for Physics, Hungarian Academy of Sciences, Konkoly-Thege M. út 29-33, H-1121 Budapest (Hungary)

2016-09-15

Complex investigations of thermostimulated luminescence (TSL) and radioluminescence properties of Li{sub 2}B{sub 4}O{sub 7} (LTB), LTB:Cu, LTB:Ag and LTB:Cu, Ag crystals suitable for tissue equivalent dosimeters were carried out in the temperature range 4.2–700 K. TSL, cathodoluminescence and X-ray excited luminescence spectra are compared to those measured under photoexcitation. The emission band at 4.6 eV in LTB:Ag is reliably related to Ag{sup +} ions based on the comparison of the results of optical spectroscopy studies and first principle calculations. Energy transfer from the relaxed exited state of the Ag{sup +} ion to the Cu{sup +} ion in double-doped LTB:Cu, Ag crystals is demonstrated. Thermostimulated recombination of charge carriers in irradiated crystals is seen to take place mainly at oxygen sites at low temperatures and at impurity sites at high temperatures. For the first time, the appearance of the low-temperature TSL peak at 90 K is assigned to ionic processes in LTB crystals. The appearance of pyroelectric flashes due to the lattice relaxation in the temperature region 90–240 K is demonstrated and their surface-related nature clarified. In accordance with EPR studies the dosimetric TSL peaks in copper and silver doped LTB crystals are attributed to thermally released electrons recombining with Cu{sup 2+} and Ag{sup 2+} centres.

[AgBr colloids prepared by electrolysis and their SERS activity research].

Science.gov (United States)

Si, Min-Zhen; Fang, Yan; Dong, Gang; Zhang, Peng-Xiang

2008-01-01

Ivory-white AgBr colloids were prepared by means of electrolysis. Two silver rods 1.0 cm in diameter and 10.0 cm long were respectively used as the negative and positive electrodes, the aqueous solution of hexadecyl trimethyl ammonium bromide was used as the electrolyte, and a 7 V direct current was applied on the silver rods for three hours. The obtained AgBr colloids were characterized by UV-Vis spectroscopy, transmission electron microscopy, and SERS using a 514. 5 nm laser line on Renishaw 2000 Raman spectrometer. These particles are about nanometer size and their shapes are as spherical or elliptic, with a slight degree of particle aggregation. The UV-Vis spectra exhibit a large plasmon resonance band at about 292.5 nm, similar to that reported in the literature. The AgBr colloids were very stable at room temperature for months. In order to test if these AgBr colloids can be used for SERS research, methyl orange, Sudan red and pyridine were used. It was found that AgBr colloids have SERS activity to these three molicules. For methyl orange, the intense Raman peaks are at 1 123, 1 146, 1 392, 1 448 and 1 594 cm(-1); for Sudan red, the intense Raman peaks are at 1 141, 1 179, 1 433 and 1 590 cm(-1); and for pyridine, the intense Raman peaks are at 1 003, 1 034 and 1 121 cm(-1). It is noticeable that SERS of methyl orange was observed on AgBr colloids, but not on the gray and yellow silver colloids prepared by traditional means. The possible reason was explained. One major advantage of this means is the absence of the spectral interference such as citrate, BH4- arising from reaction products of the colloids formation process. On AgBr colloids, one can get some molecular SERS impossible to get on the gray and yellow silver colloids.

UV-Vis spectroscopy and solvatochromism of the tyrosine kinase inhibitor AG-1478

Science.gov (United States)

Khattab, Muhammad; Wang, Feng; Clayton, Andrew H. A.

2016-07-01

The effect of twenty-one solvents on the UV-Vis spectrum of the tyrosine kinase inhibitor AG-1478 was investigated. The absorption spectrum in the range 300-360 nm consisted of two partially overlapping bands at approximately 340 nm and 330 nm. The higher energy absorption band was more sensitive to solvent and exhibited a peak position that varied from 327 nm to 336 nm, while the lower energy absorption band demonstrated a change in peak position from 340 nm to 346 nm in non-chlorinated solvents. The fluorescence spectrum of AG-1478 was particularly sensitive to solvent. The wavelength of peak intensity varied from 409 nm to 495 nm with the corresponding Stokes shift in the range of 64 nm to 155 nm (4536 cm- 1 to 9210 cm- 1). We used a number of methods to assess the relationship between spectroscopic properties and solvent properties. The detailed analysis revealed that for aprotic solvents, the peak position of the emission spectrum in wavenumber scale correlated with the polarity (dielectric constant or ET(30)) of the solvent. In protic solvents, a better correlation was observed between the hydrogen bonding power of the solvent and the position of the emission spectrum. Moreover, the fluorescence quantum yields were larger in aprotic solvents as compared to protic solvents. This analysis underscores the importance of polarity and hydrogen-bonding environment on the spectroscopic properties of AG-1478. These studies will assume relevance in understanding the interaction of AG-1478 in vitro and in vivo.

UV-Vis spectroscopy and solvatochromism of the tyrosine kinase inhibitor AG-1478.

Science.gov (United States)

Khattab, Muhammad; Wang, Feng; Clayton, Andrew H A

2016-07-05

The effect of twenty-one solvents on the UV-Vis spectrum of the tyrosine kinase inhibitor AG-1478 was investigated. The absorption spectrum in the range 300-360nm consisted of two partially overlapping bands at approximately 340nm and 330nm. The higher energy absorption band was more sensitive to solvent and exhibited a peak position that varied from 327nm to 336nm, while the lower energy absorption band demonstrated a change in peak position from 340nm to 346nm in non-chlorinated solvents. The fluorescence spectrum of AG-1478 was particularly sensitive to solvent. The wavelength of peak intensity varied from 409nm to 495nm with the corresponding Stokes shift in the range of 64nm to 155nm (4536cm(-1) to 9210cm(-1)). We used a number of methods to assess the relationship between spectroscopic properties and solvent properties. The detailed analysis revealed that for aprotic solvents, the peak position of the emission spectrum in wavenumber scale correlated with the polarity (dielectric constant or ET(30)) of the solvent. In protic solvents, a better correlation was observed between the hydrogen bonding power of the solvent and the position of the emission spectrum. Moreover, the fluorescence quantum yields were larger in aprotic solvents as compared to protic solvents. This analysis underscores the importance of polarity and hydrogen-bonding environment on the spectroscopic properties of AG-1478. These studies will assume relevance in understanding the interaction of AG-1478 in vitro and in vivo. Copyright © 2016 Elsevier B.V. All rights reserved.

Vibrational properties of epitaxial silicene layers on (1 1 1) Ag

International Nuclear Information System (INIS)

Scalise, E.; Cinquanta, E.; Houssa, M.; Broek, B. van den; Chiappe, D.; Grazianetti, C.; Pourtois, G.; Ealet, B.; Molle, A.; Fanciulli, M.; Afanas’ev, V.V.; Stesmans, A.

2014-01-01

The electronic and vibrational properties of three different reconstructions of silicene on Ag(1 1 1) are calculated and compared to experimental results. The 2D epitaxial silicon layers, namely the (4 × 4), (√13 × √13) and (2√3 × 2√3) phases, exhibit different electronic and vibrational properties. Few peaks in the experimental Raman spectrum are identified and attributed to the vibrational modes of the silicene layers. The position and behavior of the Raman peaks with respect to the excitation energy are shown to be a fundamental tool to investigate and discern different phases of silicene on Ag(1 1 1).

Vibrational properties of epitaxial silicene layers on (1 1 1) Ag

Energy Technology Data Exchange (ETDEWEB)

Scalise, E., E-mail: emilio.scalise@fys.kuleuven.be [Semiconductor Physics Laboratory, Department of Physics and Astronomy, University of Leuven, Celestijnenlaan 200 D, B-3001 Leuven (Belgium); Cinquanta, E. [Laboratorio MDM, IMM-CNR, via C. Olivetti 2, I-20864 Agrate Brianza (MB) (Italy); Houssa, M.; Broek, B. van den [Semiconductor Physics Laboratory, Department of Physics and Astronomy, University of Leuven, Celestijnenlaan 200 D, B-3001 Leuven (Belgium); Chiappe, D. [Laboratorio MDM, IMM-CNR, via C. Olivetti 2, I-20864 Agrate Brianza (MB) (Italy); Grazianetti, C. [Laboratorio MDM, IMM-CNR, via C. Olivetti 2, I-20864 Agrate Brianza (MB) (Italy); Aix-Marseille University, CNRS-CINaM, Campus de Luminy, Case 913, 13288 Marseille Cedex 09 (France); Pourtois, G. [IMEC, 75 Kapeldreef, B-3001 Leuven (Belgium); Department of Chemistry, Plasmant Research Group, University of Antwerp, B-2610 Wilrijk-Antwerp (Belgium); Ealet, B. [Aix-Marseille University, CNRS-CINaM, Campus de Luminy, Case 913, 13288 Marseille Cedex 09 (France); Molle, A. [Laboratorio MDM, IMM-CNR, via C. Olivetti 2, I-20864 Agrate Brianza (MB) (Italy); Fanciulli, M. [Laboratorio MDM, IMM-CNR, via C. Olivetti 2, I-20864 Agrate Brianza (MB) (Italy); Dipartimento di Scienza dei Materiali, Università degli Studi di Milano Bicocca, via R. Cozzi 53, I-20126 Milano (MI) (Italy); Afanas’ev, V.V.; Stesmans, A. [Semiconductor Physics Laboratory, Department of Physics and Astronomy, University of Leuven, Celestijnenlaan 200 D, B-3001 Leuven (Belgium)

2014-02-01

The electronic and vibrational properties of three different reconstructions of silicene on Ag(1 1 1) are calculated and compared to experimental results. The 2D epitaxial silicon layers, namely the (4 × 4), (√13 × √13) and (2√3 × 2√3) phases, exhibit different electronic and vibrational properties. Few peaks in the experimental Raman spectrum are identified and attributed to the vibrational modes of the silicene layers. The position and behavior of the Raman peaks with respect to the excitation energy are shown to be a fundamental tool to investigate and discern different phases of silicene on Ag(1 1 1).

Structure and photoluminescence properties of Ag-coated ZnO nano-needles

International Nuclear Information System (INIS)

Li Xiaozhu; Wang Yongqian

2011-01-01

Highlights: → ZnO nano-needles were synthesized by thermal oxidation. → Their surfaces were coated with Ag by pulse electro-deposition technique. → The uncoated and coated ZnO nano-needles were characterized. → The results showed that the prepared ZnO nano-needles have been coated with Ag successfully. → The photoluminescence spectrums of ZnO nano-needles with Ag-coated and uncoated were analyzed, finding that the Ag-coated ZnO nano-needles can increase the absorption of UV light. - Abstract: A large number of zinc oxide (ZnO) nano-needles were synthesized by thermal oxidation of pure zinc. The surfaces of ZnO nano-needles were coated with a layer of Ag by pulse electro-deposition technique. The uncoated and coated ZnO nano-needles were characterized by using the X-ray diffraction and the scanning electron microscope (SEM). The results showed that the uncoated samples were close-packed hexagonal structure, which showed needle-like morphology. Their average diameter is about 40 nm, lengths up to 5 μm. At the same time we observed that the prepared ZnO nano-needles have been coated with Ag successfully. The photoluminescence spectrums of ZnO nano-needles with Ag-coated and uncoated were analyzed, finding that the uncoated ZnO nano-needles have two fluorescence peaks at 388 nm and 470.8 nm, respectively, the relative intensity of 143.4 and 93.61; and the Ag-coated ZnO nano-needles showed a pair of strong peaks at 387.4 nm and 405.2 nm, the relative intensity of 1366 and 1305, respectively, indicating that the Ag-coated ZnO nano-needles can increase the absorption of UV light.

AG, TL, and IRSL dosimetric properties in X-ray irradiated HPHT diamond crystals

Energy Technology Data Exchange (ETDEWEB)

Gil-Tolano, M.I. [Programa de Posgrado, Departamento de Investigacion en Fisica, Universidad de Sonora, A. P. 5-088, Hermosillo, Sonora, 83190, Mexico (Mexico); Melendrez, R.; Lancheros-Olmos, J.C.; Soto-Puebla, D.; Chernov, V.; Pedroza-Montero, M.; Barboza-Flores, M. [Departamento de Investigacion en Fisica, Universidad de Sonora, A. P. 5-088, Hermosillo, Sonora, 83190, Mexico (Mexico); Castaneda, B. [Departamento de Fisica, Universidad de Sonora, Blvd. Luis Encinas y Rosales S/N, Hermosillo, Sonora, 83000, Mexico (Mexico)

2014-10-15

HPHT diamonds have been studied for several years for their potential in different applications. In previous studies it has been found that the thermoluminescence (TL) glow curves of ''as-grown'' HPHT diamonds are non-reproducible. In this work, we study the afterglow (AG), thermoluminescent (TL), and optically stimulated luminescence (OSL) response of commercial samples of synthetic HPHT type-Ib diamond crystals exposed to X-ray irradiation (0.75 mA, 35 kV) at a dose rate of 0.624 Gy/s, after a high gamma ({sup 60}Co) dose irradiation of 500 kGy followed by a thermal treatment at 1073 K for 1 h in nitrogen atmosphere. Deconvolution of the TL glow curves shows four peaks, located around 379, 509, 561, and 609 K. The crystals exhibit evident AG recorded for 300 s immediately after X-ray irradiation, due to the thermal emptying of the traps responsible for the low-temperature TL peaks (below 400 K). The stimulation of irradiated crystals with 870-nm light, creates pronounced OSL and destroys all TL peaks with the exception of the high-temperature peak at 609 K. The dose responses of the integrated AG, TL, and OSL are linear in the range of 0.6-5 Gy and saturated at higher doses. The reproducibility of AG, TL, and OSL measurements is about 5%. The fading in the first hour of storage in dark conditions at RT of TL signal of HPHT diamond is mainly associated to the emptying of the traps responsible for the 379-K TL peaks. (copyright 2014 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Optical nonlinearities in Ag/BaTiO{sub 3} multi-layer nanocomposite films

Energy Technology Data Exchange (ETDEWEB)

Yang Guang [Wuhan National Laboratory for Optoelectronics and School of Optoelectronics Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China)], E-mail: gyang@hust.edu.cn; Zhou Youhua [Wuhan National Laboratory for Optoelectronics and School of Optoelectronics Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China); School of Physics and Information Engineering, Jianghan University, Wuhan 430056 (China); Long Hua; Li Yuhua; Yang Yifa [Wuhan National Laboratory for Optoelectronics and School of Optoelectronics Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China)

2007-07-31

The multi-layer structure of barium titanate composite thin films containing Ag nanoparticles were grown on MgO (100) substrates using pulsed laser deposition technique under the nitrogen pressure of 7.4 Pa. The X-ray photoelectron spectroscopy analysis indicated that the samples were composed of metal Ag embedded in the BaTiO{sub 3} matrices. The optical absorption properties were measured from 300 nm to 800 nm, and the absorption peaks due to the surface plasmon resonance of Ag particles were observed. With the increasing of Ag concentration in composite films, the peak absorption increased and shifted to longer wavelength (red-shift). Furthermore, the third-order optical nonlinearities of the films were determined by z-scan method and the nonlinear refractive index, n{sub 2}, and nonlinear absorption coefficient, {beta}, were determined to be about - 1.91 x 10{sup -13} m{sup 2}/W and - 5.80 x 10{sup -7} m/W, respectively.

Dependence of the organic nonvolatile memory performance on the location of ultra-thin Ag film

International Nuclear Information System (INIS)

Jiao Bo; Wu Zhaoxin; He Qiang; Mao Guilin; Hou Xun; Tian Yuan

2010-01-01

We demonstrated organic nonvolatile memory devices based on 4,4',4''-tris[N-(3-methylphenyl)-N-phenylamino] triphenylamine (m-MTDATA) inserted by an ultra-thin Ag film. The memory devices with different locations of ultra-thin Ag film in m-MTDATA were investigated, and it was found that the location of the Ag film could affect the performance of the organic memory, such as ON/OFF ratio, retention time and cycling endurance. When the Ag film was located at the ITO/m-MTDATA interface, the largest ON/OFF ratio (about 10 5 ) could be achieved, but the cycling endurance was poor. When the Ag film was located in the middle region of the m-MTDATA layer, the ON/OFF ratios came down by about 10 3 , but better performance of cycling endurance was exhibited. When the Ag film was located close to the Al electrode, the ON/OFF ratios and the retention time of this device decreased sharply and the bistable phenomenon almost disappeared. Our works show a simple approach to improve the performance of organic memory by adjusting the location of the metal film.

Comparison of the two relaxation peaks in the Ti50Ni48Fe2 alloy

International Nuclear Information System (INIS)

Fan Genlian; Zhou Yumei; Otsuka, Kazuhiro; Ren Xiaobing; Suzuki, Tetsuro; Yin Fuxing

2009-01-01

The internal friction (tan δ) and storage modulus of Ti 50 Ni 48 Fe 2 alloy were studied by dynamic mechanical analysis (DMA). On cooling, a broad relaxation peak with tan δ value as high as 0.2 was detected in R-phase. On heating, another relaxation peak with tan δ value of 0.06 was found in B19' martensite. Both relaxation peaks disappeared when the alloy was dehydrogenated in a dynamic vacuum furnace. Thus, the origin of both relaxation peaks was attributed to the interaction between twin boundaries and hydrogen atoms, as recently proved in Ti-Ni-Cu alloy. The direct comparison of these two relaxation peaks in the same sample indicates that the height of relaxation peaks increases with the decreasing of twinning shear.

Mechanisms of TL for production of the 230 {sup o}C peak in natural sodalite

Energy Technology Data Exchange (ETDEWEB)

Cano, Nilo F., E-mail: nilocano@dfn.if.usp.b [Institute of Physics, University of Sao Paulo, Rua do Matao, Travessa R, 187, CEP 05508-090, Sao Paulo (Brazil); Professional School of Physics, University of San Agustin of Arequipa, Av. Independencia S/N, Arequipa (Peru); Blak, Ana R. [Institute of Physics, University of Sao Paulo, Rua do Matao, Travessa R, 187, CEP 05508-090, Sao Paulo (Brazil); Ayala-Arenas, Jorge S. [Professional School of Physics, University of San Agustin of Arequipa, Av. Independencia S/N, Arequipa (Peru); Watanabe, Shigueo [Institute of Physics, University of Sao Paulo, Rua do Matao, Travessa R, 187, CEP 05508-090, Sao Paulo (Brazil)

2011-02-15

The thermoluminescence (TL) peak in natural sodalite near 230 {sup o}C, which appears only after submitted to thermal treatments and to gamma irradiation, has been studied in parallel with electron paramagnetic resonance (EPR) spectrum appearing under the same procedure. This study revealed a full correlation between the 230 {sup o}C TL peak and the eleven hyperfine lines from EPR spectrum. In both case, the centers disappear at the same temperature and are restored after gamma irradiation. A complete model for the 230 {sup o}C TL peak is presented and discussed. In addition to the correlation and TL model, specific characteristics of the TL peaks are described.

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.

Understanding the growth mechanism of stabilizer-free Ag nanoparticles on reduced graphene oxide: the role of CO

International Nuclear Information System (INIS)

Gao Weiyin; Ran Chenxin; Wang Minqiang; Yao Xi; He Delong; Bai Jinbo

2013-01-01

In this study, one-step approach to prepare stabilizer-free Ag–graphene nanocomposites using DMAc-assisted thermal reduction method with uniform distribution of “near spherical” Ag nanoparticles (Ag NPs) in the range of 16–20 nm is reported. Interestingly, from the change of absorption spectrum as a function of reaction time, we observed that the characteristic absorption peak of Ag NPs shows no peak position shift in a quite long time without extra stabilizer while red-shift and broaden after continuous reaction. To explain this phenomenon, we further proposed a growth mechanism that CO, which is generated from reduction of functional groups on GO, adsorbed on the surface of Ag NPs and leaded to growth cease of Ag NPs into a narrow size distribution during the reduction of GO. Meanwhile, Ag NPs can catalyze the oxidation of adsorbed-CO to CO 2 in the presence of O 2 which can easily desorb from Ag surfaces. Hence, after fully removal of functional groups on GO, continuous supply of CO was cutoff while the desorption of adsorbed-CO was still happening continually, so Ag NPs start to gradually grow and resulting in aggregation. Moreover, the dosage of less DMAc or more AgNO 3 would cause the anisotropic growth and form multiply twinned structure of Ag NPs. Our study presents a useful understanding on the growth of Ag NPs on graphene.

Ag/Pd core-shell nanoparticles by a successive method: Pulsed laser ablation of Ag in water and reduction reaction of PdCl{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Mottaghi, N. [Department of Physics, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Ranjbar, M., E-mail: ranjbar@cc.iut.ac.ir [Department of Physics, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Farrokhpour, H. [Department of Chemistry, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Khoshouei, M. [Max Planck Institute of Biochemistry, Department of Molecular Structural Biology, Am Klopferspitz 18, Martinsried 82152 (Germany); Khoshouei, A.; Kameli, P.; Salamati, H. [Department of Physics, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Tabrizchi, M. [Department of Chemistry, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of); Jalilian-Nosrati, M. [Physics department, Central Azad University, Tehran 14676-86831 (Iran, Islamic Republic of)

2014-02-15

In this study Ag/Pd nanoparticles (NPs) have been fabricated by a successive method; first, colloids of Ag nanoparticles (NPs) have been prepared in water by pulsed laser ablation in liquid (PLAL) method. Then PdCl{sub 2} solution (up to 0.2 g/l) were added to the as-prepared or aged colloidal Ag NPs. Characterizations were done using UV–vis spectroscopy, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and transmissions electron microscopy (TEM) techniques. Spectroscopy data showed that surface plasmon resonance (SPR) peaks of as-prepared Ag NPs at about λ = 400 nm were completely extinguished after addition of PdCl{sub 2} solution while this effect was not observed when aged Ag NPs are used. XRD and XPS results revealed that by addition of the PdCl{sub 2} solution into the as-prepared Ag NPs, metallic palladium, and silver chloride composition products are generated. TEM images revealed that as a result of this reaction, single and core-shell nanoparticles are obtained and their average sizes are 2.4 nm (Ag) and 3.2 nm (Ag/Pd). The calculated d-spacing values form XRD data with observations on high magnification TEM images were able to explain the chemical nature of different parts of Ag/Pd NPs.

Synthesis and antibacterial evaluation of calcinated Ag-doped nano-hydroxyapatite with dispersibility.

Science.gov (United States)

Furuzono, Tsutomu; Motaharul, Mazumder; Kogai, Yasumichi; Azuma, Yoshinao; Sawa, Yoshiki

2015-05-01

Dispersible hydroxyapatite (HAp) nanoparticles are very useful for applying a monolayer to implantable medical devices using the nano-coating technique. To improve tolerance to infection on implanted medical devices, silver-doped HAp (Ag-HAp) nanoparticles with dispersiblity and crystallinity were synthesized, avoiding calcination-induced sintering, and evaluated for antibacterial activity. The Ca10-xAgx(PO4)6(OH)2 with x = 0 and 0.2 were prepared by wet chemical processing at 100°C. Before calcination at 700°C for 2 h, two kinds of anti-sintering agents, namely a Ca(NO3)2 (Ca salt) and a polyacrylic acid/Ca salt mixture (PAA-Ca), were used. Escherichia coli was used to evaluate the antibacterial activity of the nanopowder. When PAA-Ca was used as an anti-sintering agent in calcination to prepare the dispersible nanoparticles, strong metallic Ag peaks were observed at 38.1° and 44.3° (2θ) in the X-ray diffraction (XRD) profile. However, the Ag peak was barely observed when Ca salt was used alone as the anti-sintering agent. Thus, using Ca salt alone was more effective for preparation of dispersible Ag-HAp than PAA-Ca. The particle average size of Ag-HAp with 0.5 mol% of Ag content was found to be 325 ± 70 nm when the formation of large particleaggregations was prevented, as determined by dynamic light scattering instrument. The antibacterial activity of the Ag-HAp nanoparticles possessing 0.5 mol% against E. coli was greater than 90.0%. Dispersible and crystalline nano Ag-HAp can be obtained by using Ca salt alone as an anti-sintering agent. The nanoparticles showed antibacterial activity.

Ag-Coated Heterostructures of ZnO-TiO2/Delaminated Montmorillonite as Solar Photocatalysts

Directory of Open Access Journals (Sweden)

Carolina Belver

2017-08-01

Full Text Available Heterostructures based on ZnO-TiO2/delaminated montmorillonite coated with Ag have been prepared by sol–gel and photoreduction procedures, varying the Ag and ZnO contents. They have been thoroughly characterized by XRD, WDXRF, UV–Vis, and XPS spectroscopies, and N2 adsorption, SEM, and TEM. In all cases, the montmorillonite was effectively delaminated with the formation of TiO2 anatase particles anchored on the clay layer’s surface, yielding porous materials with high surface areas. The structural and textural properties of the heterostructures synthesized were unaffected by the ZnO incorporated. The photoreduction led to solids with Ag nanoparticles decorating the surface. These materials were tested as photocatalysts for the degradation of several emerging contaminants with different nitrogen-bearing chemical structures under solar light. The catalysts yielded high rates of disappearance of the starting pollutants and showed quite stable performance upon successive applications.

The Effect of Cu:Ag Atomic Ratio on the Properties of Sputtered Cu–Ag Alloy Thin Films

Directory of Open Access Journals (Sweden)

Janghsing Hsieh

2016-11-01

Full Text Available Cu–Ag thin films with various atomic ratios were prepared using a co-sputtering technique, followed by rapid thermal annealing at various temperatures. The films’ structural, mechanical, and electrical properties were then characterized using X-ray diffractometry (XRD, atomic force microscopy (AFM, FESEM, nano-indentation, and TEM as functions of compositions and annealing conditions. In the as-deposited condition, the structure of these films transformed from a one-phase to a dual-phase state, and the resistivity shows a twin-peak pattern, which can be explained in part by Nordheim’s Rule and the miscibility gap of Cu–Ag alloy. After being annealed, the films’ resistivity followed the mixture rule in general, mainly due to the formation of a dual-phase structure containing Ag-rich and Cu-rich phases. The surface morphology and structure also varied as compositions and annealing conditions changed. The recrystallization of these films varied depending on Ag–Cu compositions. The annealed films composed of 40 at % to 60 at % Cu had higher hardness and lower roughness than those with other compositions. Particularly, the Cu50Ag50 film had the highest hardness after being annealed. From the dissolution testing, it was found that the Cu-ion concentration was about 40 times higher than that of Ag. The galvanic effect and over-saturated state could be the cause of the accelerated Cu dissolution and the reduced dissolution of the Ag.

Translocation, accumulation and distribution of 110mAg in carp

International Nuclear Information System (INIS)

Li Chuanzhao; Zhao Wenhu; Xu Shiming

1995-01-01

The experimental carp were raised in the water with 110m Ag specific activity of 3.7 x 10 2 Bq/L, 3.7 x 10 3 Bq/L, 3.7 x 10 4 Bq/L respectively. The carp were sampled after raising 1,2,3,5,7,9,12,15,18,21 and 23 days, and separated into scale, bone, muscle, gill, alimentary canal, heart and heptapancreas for measuring the radioactivity. The results showed that 110m Ag was absorbed rapidly by carp via gill and alimentary canal from water, and distributed into all parts of the body, mainly in soft tissue with blood circulation. 110m Ag accumulation of the body increased with the 110m Ag specific activity in the water in the same raising time. The accumulation of 110m Ag in gill, alimentary canal, heart, muscle and bone appeared mono-peak curves with raising time. There was a linear relationship between the specific activity of 110m Ag in heptapancreas and the carp's raising time in 110m Ag water. The concentration abilities for 110m Ag in all organs were in the order of heptapancreas>gill>alimentary>canal>heart>muscle>bone

Sensors based on Ag-loaded hematite (α-Fe2O3 nanoparticles for methyl mercaptan detection at room temperature

Directory of Open Access Journals (Sweden)

Daniel Garcia

2017-06-01

Full Text Available Sensors based on Ag/α-Fe2O3 nanoparticles have been prepared by the coprecipitation method for sensing methyl mercaptan at room temperature. X-ray diffraction patterns of samples matched perfectly with characteristic peaks of hematite with no peaks assigned to Ag even at the highest concentration. STEM images and EDX analysis revealed the presence of Ag nanoparticles (from 2 to 5 nm which were highly dispersed onto α-Fe2O3 surface with an Ag/Fe ratio from 0.014 to 0.099. The Ag nanoparticles were deposited on the hematite surface. Sensing tests of Ag-loaded hematite nanoparticles showed much higher response signal than the unmodified sensor. Hematite loaded with 3%(Wt Ag showed the highest response with a linear dependence from 20 to 80 ppm. The sensor also depicted a good selectivity and stability during 4 days with short recovery time. The high dispersion of reduced Ag evaluated by XPS analysis played an important chemical role in the sensing mechanism that favored the contact of CH3SH with oxygen.

Disruption of crystalline structure of Sn3.5Ag induced by electric current

International Nuclear Information System (INIS)

Huang, Han-Chie; Lin, Kwang-Lung; Wu, Albert T.

2016-01-01

This study presented the disruption of the Sn and Ag_3Sn lattice structures of Sn3.5Ag solder induced by electric current at 5–7 × 10"3 A/cm"2 with a high resolution transmission electron microscope investigation and electron diffraction analysis. The electric current stressing induced a high degree of strain on the alloy, as estimated from the X-ray diffraction (XRD) peak shift of the current stressed specimen. The XRD peak intensity of the Sn matrix and the Ag_3Sn intermetallic compound diminished to nearly undetectable after 2 h of current stressing. The electric current stressing gave rise to a high dislocation density of up to 10"1"7/m"2. The grain morphology of the Sn matrix became invisible after prolonged current stressing as a result of the coalescence of dislocations.

The AGS Booster main ring power supply system

International Nuclear Information System (INIS)

Soukas, A.; Hughes, K.; Sandberg, J.; Toldo, F.; Zhang, S.Y.

1989-01-01

The AGS Booster is being designed as a very versatile particle accelerator. Its primary function is to be a high quality injector to the currently operating Alternating Gradient Synchrotron (AGS). The Booster/AGS combination will produce proton intensities greater than 5 x 10 13 protons per pulse (ppp), and accelerate heavy ions, with mass up to 200, to a maximum energy of 15 GeV per atomic mass unit (GeV/amu). The power supply for the Booster Main Ring (BMRPS) has to accommodate a wide range of cycles and a wide range of operating parameters. The cycles range from storage for several seconds to rapid cycling at 7.5 Hz. The peak output power is 18 MW. This paper will describe the AGS Booster machine powering requirements, the choice of power supply, the a.c. circuit tie-in and its associated problems and some of the details of the design of the BMRPS. 9 refs., 2 figs

[Effects of silver nitrate on the phase state of model multibilayer membranes].

Science.gov (United States)

Vashchenko, O V; Iermak, Yu L; Krasnikova, A O; Lisetski, L N

2015-01-01

In order to study the effects caused by silver nitrate (AgNO3) on model lipid membranes, we studied multibilayer membranes based on L-α-dipalmitoylphosphatidylcholine (DPPC) and AgNO3 aqueous soluitions in a wide concentration range (up to 30 wt%) by means of differential scanning calorimetry. It has been shown that the presence of AgNO3 leads both to an increase in the main phase transition temperature (T(m)) and appearance of an additional phase transition peak (T(m)), suggesting increasing of both density and heterogeneity of the lipid membrane. The effect of nitrate ions (NO ) was shown to be of the opposite nature (bilayer fluidizing), so the integral densifying effect of AgNO3 can be referred solely to the action of silver ions (Ag(+)). With increasing AgNO3 concentration, the tendency was observed to opposite changes in T(m) and T'(m) peaks intensity, thereby at about 26. wt% of AgNO3 the initial peak (T(m)) disappeared. In the range of Ag+ therapeutic concentrations (up to 2 wt%) no significant changes in the DPPC membrane were revealed. This can be one of the reasons of the absence of a damaging effect of silver drugs on a host organism with simultaneous pronounced bactericidal effect.

Sn-In-Ag phase equilibria and Sn-In-(Ag)/Ag interfacial reactions

International Nuclear Information System (INIS)

Chen Sinnwen; Lee Wanyu; Hsu Chiaming; Yang Chingfeng; Hsu Hsinyun; Wu Hsinjay

2011-01-01

Research highlights: → Thermodynamic models of Sn-In and Sn-In-Ag are developed using the CALPHAD approach. → Reaction layer in the Sn-In-(Ag)/Ag couples at 100 deg. C is thinner than those at 25 deg. C, 50 deg. C, and 75 deg. C. → Reactions in the Sn-20 wt%In-2.8 wt%Ag/Ag couples are faster than those in the Sn-20 wt%In/Ag couples. - Abstract: Experimental verifications of the Sn-In and Sn-In-Ag phase equilibria have been conducted. The experimental measurements of phase equilibria and thermodynamic properties are used for thermodynamic modeling by the CALPHAD approach. The calculated results are in good agreement with experimental results. Interfacial reactions in the Sn-In-(Ag)/Ag couples have been examined. Both Ag 2 In and AgIn 2 phases are formed in the Sn-51.0 wt%In/Ag couples reacted at 100 and 150 deg. C, and only the Ag 2 In phase is formed when reacted at 25, 50 and 75 deg. C. Due to the different growth rates of different reaction phases, the reaction layer at 100 deg. C is thinner than those at 25 deg. C, 50 deg. C, and 75 deg. C. In the Sn-20.0 wt%In/Ag couples, the ζ phase is formed at 250 deg. C and ζ/AgIn 2 phases are formed at 125 deg. C. Compared with the Sn-20 wt%In/Ag couples, faster interfacial reactions are observed in the Sn-20.0 wt%In-2.8 wt%Ag/Ag couples, and minor Ag addition to Sn-20 wt%In solder increases the growth rates of the reaction phases.

Gamma-irradiation assisted seeded growth of Ag nanoparticles within PVA matrix

International Nuclear Information System (INIS)

Eisa, Wael H.; Abdel-Moneam, Yasser K.; Shaaban, Yasser; Abdel-Fattah, Atef A.; Abou Zeid, Amira M.

2011-01-01

Highlights: → Nucleation and growth must be two completely separated steps. → The amount of zerovalent nuclei can be controlled by varying the irradiation dose. → PVA act as physical barrier to inhibit aggregation or the growth of Ag nanoparticles. - Abstract: Polyvinyl alcohol (PVA)/Ag hybrid nanocomposites have been prepared from polymeric film of PVA and silver nitrate (AgNO 3 ). The silver nanoparticles were generated in PVA matrix by the reduction of silver ions with gamma-irradiation. UV-visible spectra showed a single peak at 422 nm, arising from the surface plasmon absorption of silver nanoparticles. The shifting of surface plasmon resonance peak after irradiation reveals that the gamma irradiation can be used as a size controlling agent for the preparation of silver nanoparticles embedded in PVA film. This result was in good agreement with the result obtained from TEM images. The TEM images showed the narrow size distribution of the obtained Ag nanoparticles with average particle size of 30 nm, which decreased to 17 nm with increasing irradiation dose. The X-ray diffraction analysis revealed that silver metal was present in face centered cubic (fcc) crystal structure. These results clearly indicate that monodispersed silver nanoparticles are embedded homogenously in PVA matrix.

Dependence of nonlinear optical properties of Ag2S@ZnS core-shells on Zinc precursor and capping agent

Science.gov (United States)

Dehghanipour, M.; Khanzadeh, M.; Karimipour, M.; Molaei, M.

2018-03-01

In this research, four different types of Ag2S@ZnS core-shells were synthesized and their nonlinear optical (NLO) properties were investigated using a Z-scan technique by a 532 nm laser diode. Here, Ag2S and ZnS nanoparticles were also synthesized and their NLO properties were compared with Ag2S@ZnS core-shells. It was observed that the NLO properties of Ag2S@ZnS quantum dots significantly increased by increasing the values of Zn(NO3)2 and thioglycolic acid (TGA). It was also observed that the NLO properties of Ag2S@ZnS core-shells for 0.1 g of Zn(NO3)2 and 7000 μl TGA is higher than sole Ag2S and ZnS nanoparticles. In open aperture Z-scan curve of ZnS sample, a saturable absorption peak was observed and this peak was seen also in type of Ag2S@ZnS nanoparticles which the value of Zn(NO3)2 much more.

Disruption of crystalline structure of Sn3.5Ag induced by electric current

Energy Technology Data Exchange (ETDEWEB)

Huang, Han-Chie; Lin, Kwang-Lung, E-mail: matkllin@mail.ncku.edu.tw [Department of Material Science and Engineering, National Cheng Kung University, Tainan 70101, Taiwan (China); Wu, Albert T. [Department of Chemical and Material Engineering, National Central University, Jhongli 32001, Taiwan (China)

2016-03-21

This study presented the disruption of the Sn and Ag{sub 3}Sn lattice structures of Sn3.5Ag solder induced by electric current at 5–7 × 10{sup 3} A/cm{sup 2} with a high resolution transmission electron microscope investigation and electron diffraction analysis. The electric current stressing induced a high degree of strain on the alloy, as estimated from the X-ray diffraction (XRD) peak shift of the current stressed specimen. The XRD peak intensity of the Sn matrix and the Ag{sub 3}Sn intermetallic compound diminished to nearly undetectable after 2 h of current stressing. The electric current stressing gave rise to a high dislocation density of up to 10{sup 17}/m{sup 2}. The grain morphology of the Sn matrix became invisible after prolonged current stressing as a result of the coalescence of dislocations.

Optically stimulated luminescence (OSL) from Ag-doped Li{sub 2}B{sub 4}O{sub 7} crystals

Energy Technology Data Exchange (ETDEWEB)

Kananen, B.E.; Maniego, E.S.; Golden, E.M.; Giles, N.C.; McClory, J.W. [Department of Engineering Physics, Air Force Institute of Technology, Wright-Patterson Air Force Base, OH 45433 (United States); Adamiv, V.T.; Burak, Ya.V. [Vlokh Institute of Physical Optics, Dragomanov 23, L’viv 79005 (Ukraine); Halliburton, L.E., E-mail: Larry.Halliburton@mail.wvu.edu [Department of Physics and Astronomy, West Virginia University, Morgantown, WV 26506 (United States)

2016-09-15

Optically stimulated luminescence (CW-OSL) is observed from Ag-doped lithium tetraborate (Li{sub 2}B{sub 4}O{sub 7}) crystals. Photoluminescence, optical absorption, and electron paramagnetic resonance (EPR) are used to identify the defects participating in the OSL process. As-grown crystals have Ag{sup +} ions substituting for Li{sup +} ions. They also have Ag{sup +} ions occupying interstitial sites. During a room-temperature exposure to ionizing radiation, holes are trapped at the Ag{sup +} ions that replace Li{sup +} ions and electrons are trapped at the interstitial Ag{sup +} ions, i.e., the radiation forms Ag{sup 2+} (4d{sup 9}) ions and Ag{sup 0} (4d{sup 10}5s{sup 1}) atoms. These Ag{sup 2+} and Ag{sup 0} centers have characteristic EPR spectra. The Ag{sup 0} centers also have a broad optical absorption band peaking near 370 nm. An OSL response is observed when the stimulation wavelength overlaps this absorption band. Specifically, stimulation with 400 nm light produces an intense OSL response when emission is monitored near 270 nm. Electrons optically released from the Ag{sup 0} centers recombine with holes trapped at Ag{sup 2+} ions to produce the ultraviolet emission. The OSL response is progressively smaller as the stimulation light is moved to longer wavelengths (i.e., away from the 370 nm peak of the absorption band of the Ag{sup 0} electron traps). Oxygen vacancies are also present in the Ag-doped Li{sub 2}B{sub 4}O{sub 7} crystals, and their role in the OSL process as a secondary relatively short-lived electron trap is described.

High-temperature peaks of thermostimulated luminescence in the ammonium halogens

International Nuclear Information System (INIS)

Kim, L.M.; Musenova, Eh.K.; Mukhamedrakhimov, K.U.

2003-01-01

The ammonium halogen crystals (AHC) are the close analogs of the alkali halogen crystals by the type of chemical bonds and crystal lattice structure. The ammonium halogen after irradiation by X-rays within 80-300 K range have two peaks of thermo-stimulation luminescence. Its maximums in dependence of anions type are in the 110-120 K and 170-180 K ranges. The first range is related with activation of auto-localized holes migration, and the second one - with the NH 3 + defects decay. Experimentally is established, that the pure ammonium halogens have memory about the previous irradiation at heating up to 300 K. After repeat irradiation the recombination luminescence high-temperature peak's shoulder is appearing. The second luminescence peak's shoulder revealing does not depend on the impurity center nature. It is known, that in the AHC there is the next thermo-stimulation luminescence peak within 340-360 K. The thermal annealing of this peak leads to the memory effect disappearance. So, the observing phenomenon is related with own defect of the matrix in the cation sublattice. Experimentally is established, that at a room temperature the AHC memorizing about previous irradiation during 20 h

Nanoscale coupling of photons to vibrational excitation of Ag nanoparticle 2D array studied by scanning tunneling microscope light emission spectroscopy.

Science.gov (United States)

Katano, Satoshi; Toma, Koji; Toma, Mana; Tamada, Kaoru; Uehara, Yoichi

2010-11-28

Scanning tunneling microscope light emission (STM-LE) spectroscopy has been utilized to elucidate the luminescence phenomena of Ag nanoparticles capped with myristate (myristate-capped AgNP) and 2-methyl-1-propanethiolate (C(4)S-capped AgNP) on the dodecanethiol-precovered Au substrate. The STM imaging revealed that myristate-capped AgNPs form an ordered hexagonal array whereas C(4)S-capped AgNPs show imperfect ordering, indicating that a shorter alkyl chain of C(4)S-capped AgNP is not sufficient to form rigid interdigitation. It should be noted that such a nanoparticle ordering affects the luminescence properties of the Ag nanoparticle. We found that the STM-LE is only detected from the Ag nanoparticles forming the two-dimensional superlattice. This indicates that the STM-LE of the Ag nanoparticle is radiated via the collective excitation of the local surface plasmon resonance (LSPR) spread over the Ag nanoparticles. Note that the STM-LE spectra of the Ag nanoparticles exhibit spike-like peaks superimposed on the broad light emission peak. Using Raman spectroscopy, we concluded that the spike-like structure appearing in the STM-LE spectra is associated with the vibrational excitation of the molecule embedded between Ag nanoparticles.

Plants for H- acceleration in the AGS Linac

International Nuclear Information System (INIS)

Barton, D.S.; Witkover, R.L.

1979-01-01

Since its commissioning in 1970, the 200 MeV Linac at the Brookhaven AGS has been capable of producing peak proton beam current of greater than 100 mA with pulse lengths up to 300 μsec at a repetition rate of 10 pulses/second. The linac typically runs at 5 pulses per second, providing a 60 mA pulse of 120 μsec duration every 1.6 to 2.4 seconds for conventional multiturn injection into the AGS. The intervening pulses of length up to 300 μsec are used by the radio-isotope production, chemistry and medical facilities. Preparations are now being made to inject and accelerate H - ions in order to implement charge exchange injection into the AGS. This paper describes the aspects of this work leading to an H - beam at 200 MeV

Tunneling-recombination luminescence between Ag0 and Ag2+ in KCl:AgCl

International Nuclear Information System (INIS)

Delbecq, C.J.; Dexter, D.L.; Yuster, P.H.

1978-01-01

Appropriate treatment of a KCl:AgCl crystal results in the trapping of electrons as silver atoms, Ag 0 , and positive holes as AgCl 4 2- , Ag 2+ , centers. Optical excitation of Ag 0 in such a crystal at T 0 and Ag 2+ pairs, similar to the Ag 0 -Cl 2 - tunneling-recombination studies we previously reported. We have shown that Ag 2+ centers are involved in the emission process by preferentially orienting the anisotropic Ag 2+ at 6 K by excitation with polarized light and observing that the afterglow is polarized. Upon warming to 50 K, where the preferentially oriented Ag 2+ can change orientation, a strong reversal in the degree of polarization occurs which finally decays to zero. The characteristics of this luminescence can be understood if we assume: (i) a tunneling-recombination mechanism in which the orientation of the electric vector of the emitted radiation depends on the position of the Ag 0 relative to the Ag 2+ and (ii) the tunneling is anisotropic and depends on the location of the Ag 0 relative to the anisotropic Ag 2+ . The latter assumption is based on the tetragonal (d-like) symmetry of the Ag 2+ complex. Good quantitative agreement between theory and experiment has been obtained on the decay kinetics, the degree of polarization, and the polarization reversal

The preparation of Ag-BiVO4 metal composite oxides and its application in efficient photocatalytic oxidative thiophene

Science.gov (United States)

Gao, Xiao-Ming; Fu, Feng; Zhang, Li-Ping; Li, Wen-Hong

2013-06-01

A series of Ag-BiVO4 photocatalysts was synthesized by the hydrothemal synthesis method for different pH values. A strong correlation was found among the prepared processing, structure and property of the samples. With increasing pH value from 5 to 9, the crystallinity increases and the as-prepared Ag-BiVO4 sample gradually disappeared from the nanostructures. The light absorption became higher in the UV and visible range, accompanied by a bathochromic shift of the absorption edge. The competitive relations between crystallinity and surface area affecting photocatalytic activity were also discussed. Photocatalytic desulfurization on the as-prepared Ag-BiVO4 samples using thiophene dissolved in n-octane as a model organosulfur compound was performed. It showed that the photocatalytic desulfurization on the as-prepared Ag-BiVO4 sample at pH=7 can be up to 95%, which existed as various size particles and had significant high surface area of 13.768 m2 g-1.

Construction of Ag/AgCl nanostructures from Ag nanoparticles as high-performance visible-light photocatalysts

Energy Technology Data Exchange (ETDEWEB)

Yang, Fan; Liu, Dongzhi; Wang, Tianyang; Li, Wei [Tianjin University, School of Chemical Engineering and Technology (China); Hu, Wenping [Tianjin University, Collaborative Innovation Center of Chemical Science and Engineering (China); Zhou, Xueqin, E-mail: zhouxueqin@tju.edu.cn [Tianjin University, School of Chemical Engineering and Technology (China)

2016-11-15

A combined strategy of in situ oxidation and assembly is developed to prepare Ag/AgCl nanospheres and nanocubes from Ag nanoparticles under room temperature. It is a new facile way to fabricate Ag/AgCl with small sizes and defined morphologies. Ag/AgCl nanospheres with an average size of 80 nm were achieved without any surfactants, while Ag/AgCl nanocubes with a mean edge length of 150 nm were obtained by introduction of N-dodecyl-N,N-dimethyl-2-ammonio-acetate. The possible formation mechanism involves the self-assembly of AgCl nanoparticles, Ostwald ripening and photoreduction of Ag{sup +} into Ag{sup 0} by the room light. The as-prepared Ag/AgCl nanospheres and nanocubes exhibit excellent photocatalytic activity and stability toward degradation of organic pollutants under visible-light irradiation. It is demonstrated that Ag/AgCl nanocubes display enhanced photocatalytic activity in comparison with Ag/AgCl nanospheres due to the more efficient charge transfer. This work may pave an avenue to construct various functional materials via the assembly strategy using nanoparticles as versatile building blocks.

Effect of Ag Doping on the Electronic Structure and Optical Properties of ZnO(0001 Surface

Directory of Open Access Journals (Sweden)

Xiang Qian

2018-01-01

Full Text Available Using first-principle calculations, the geometrical structure, the electronic and optical properties of Ag-doped ZnO(0001 surface have been investigated. We found that Ag-doped ZnO(0001 surface is more easily formed on the first layer. On the other hand, the doped surface has gradually become an equipotential body, showing obvious metallic characteristics. We found that a new peak appeared in the low energy region after Ag doping, which was mainly due to the electron transition between the two orbital levels of Ag-4d and O-2p.

XPS and Ag L3-edge XANES characterization of silver and silver-gold sulfoselenides

Science.gov (United States)

Mikhlin, Yuri L.; Pal'yanova, Galina A.; Tomashevich, Yevgeny V.; Vishnyakova, Elena A.; Vorobyev, Sergey A.; Kokh, Konstantin A.

2018-05-01

Gold and silver sulfoselenides are of interest as materials with high ionic conductivity and promising magnetoresistive, thermoelectric, optical, and other physico-chemical properties, which are strongly dependent on composition and structure. Here, we applied X-ray photoelectron spectroscopy and Ag L3 X-ray absorption near-edge structure (XANES) to study the electronic structures of low-temperature compounds and solid solutions Ag2SxSe1-x (0 compounds; in particular, the Ag L3-edge peak is about 35% lower for AgAuS relative to Ag2S. At the same time, the Au 4f binding energy and, therefore, charge at Au(I) sites increase with increasing S content due to the transfer of electron density from Au to Ag atoms. It was concluded that the effects mainly originate from shortening of the metal-chalcogen and especially the Ausbnd Ag interatomic distances in substances having similar coordination geometry.

The formation and disappearance of filament barbs observed by SDO

Science.gov (United States)

Li, Leping; Zhang, Jun

2014-01-01

Employing six-day (August 16-21, 2010) SDO/AIA observations, we systematically investigate the formation and disappearance of 58 barbs of a northern (~N60) polar crown filament. Three different ways of barb formation are discovered, including (1) the convergence of surrounding moving materials (55.2%), (2) the flows of materials from the filament (37.9%), and (3) the material injections from neighboring brightening regions (6.9%). We also find three different types of barb disappearance, involving: (i) the bi-lateral movements (44.8%), and (ii) the outflowing (27.6%) of barb material resulting in the barb disappearance, as well as (iii) the barb disappearance associated with neighboring brightenings (27.6%). We propose that barbs exchange materials with the filament, surrounding atmosphere, and nearby brightening regions, causing the barb formation and disappearance.

Influence of Ag doping on structural, optical, and photoluminescence properties of nanostructured AZO films by sol–gel technique

International Nuclear Information System (INIS)

Khan, Firoz; Baek, Seong-Ho; Kim, Jae Hyun

2014-01-01

Graphical abstract: The optical band gap of the Ag–AZO film first decreased to a value of ∼3.31 eV for a 1% Ag/Zn atomic ratio from a value of ∼3.69 for undoped AZO film. For higher values (beyond a 1% Ag/Zn atomic ratio) of Ag doping, the values of Eg started to increase and finally attained a value of ∼3.66 eV for an Ag/Zn 3% atomic ratio. The photoluminescence (PL) studies showed that the relative PL intensity of the Ag–AZO films in blue (IB) and green (IG) regions increased with Ag doping. The PL positions of these peaks were blue shifted with increased Ag content up to an Ag/Zn atomic ratio of 3%. The increase in IB and IG is due to the charge difference between Ag + and Zn 2+ , whereas shifting of the PL positions is due to the size of Ag + and Zn 2+ ions. -- Highlights: • The optical band gap of the Ag–AZO film is tuned with Ag doping. • The PL intensity of the Ag–AZO film in visible region is increased with Ag doping. • The PL positions of these peaks were blue shifted with increased Ag content. • The increase in I B and I G is due to the charge difference between Ag + and Zn 2+ . • The shifting of the PL positions is due to the size of Ag + and Zn 2+ ions. -- Abstract: The effects of Ag doping on the structural, electrical, optical, and photoluminescence properties of sol-gel derived Al rich zinc oxide (Ag–AZO) films are studied. The Al/Zn atomic ratio was constant (∼20%) in all the films, whereas the Ag/Zn atomic ratio varied from 0% to 3%. All the films were highly transparent in the 400–1200 nm wavelength range. The XRD results and surface morphologies of the films confirmed that the grain size increased with Ag doping. The optical band gap (E g ) of the Ag–AZO film first decreased to a value of ∼3.31 eV for a 1% Ag/Zn atomic ratio from a value of ∼3.69 for undoped AZO film. For higher values (beyond a 1% Ag/Zn atomic ratio) of Ag doping, the values of E g started to increase and finally attained a value of ∼3.66 e

Work function tuning and fluorescence enhancement of hydrogen annealed Ag-doped Al-rich zinc oxide nanostructures using a sol–gel process

Energy Technology Data Exchange (ETDEWEB)

Khan, Firoz; Baek, Seong-Ho [Energy Research Division, Daegu Gyeongbuk Institute of Science & Technology (DGIST), 50-1 Sang-Ri, Hyeonpung-Myeon, Dalseong-Gun, Daegu 711-873 (Korea, Republic of); Lee, Jae Young [School of Mechanical and Control Engineering, Handong Global University, 558 Handong-Ro, Heunghae-Eub, Buk-Ku, Pohang, Gyung-Buk 791-708 (Korea, Republic of); Kim, Jae Hyun, E-mail: jaehyun@dgist.ac.kr [Energy Research Division, Daegu Gyeongbuk Institute of Science & Technology (DGIST), 50-1 Sang-Ri, Hyeonpung-Myeon, Dalseong-Gun, Daegu 711-873 (Korea, Republic of)

2015-10-25

Effect of incorporation of Ag on the structural, optical, electrical, and fluorescence properties of sol–gel derived Al-rich zinc oxide (ZnO:Al:Ag) nanostructured films was studied. The E{sub g} of the film slightly decreased to a minimal value with Ag doping, and was found to be about 3.65 eV for R{sub Ag/Zn} = 1% from its initial value of 3.72 eV (R{sub Ag/Zn} = 0%). The WF sudden increased to a maximal value of 5.12 eV with Ag doping (for R{sub Ag/Zn} = 1%) from its initial value of 4.73 eV for R{sub Ag/Zn} = 0% due to substitution of Ag into Zn sites until saturation was achieved (R{sub Ag/Zn} = 1%). After more Ag doping, WF started to decrease and finally, reached a value of 4.81 eV for R{sub Ag/Zn} = 3% because of the formation of an impurity-defect energy level below the intrinsic Fermi level of ZnO. With Ag-doping, the current increased up to R{sub Ag/Zn} = 1% due to the increase in carrier density. For R{sub Ag/Zn} = 3% doping, the current density started to increase due to the influence of metallic Ag. The defective peak position was blue shifted, with increased Ag-doping, from 536 nm (R{sub Ag/Zn} = 1%) to 527 nm for R{sub Ag/Zn} = 2% due to the sizes of the Ag{sup +} and Zn{sup 2+} ions. The FL defective peak intensity (I{sub D}) in the green region increased with the concentration of Ag used for doping, up to R{sub Ag/Zn} = 2%. The enhancement in the I{sub D} may be due to charge difference between the Zn{sup 2+} ions, caused by Ag{sup +} ions. - Graphical abstract: The effect of incorporation of Ag doping on the structural, optical, electrical, and fluorescence properties of sol–gel derived Al-rich zinc oxide (ZnO:Al:Ag) nanostructured films was studied. By Ag-doping, the lowest R{sub λ} is blue shifted to R{sub Ag/Zn} = 2% and finally red shifted for R{sub Ag/Zn} = 3% due to variation of optical thickness of the film. The E{sub g} of the film slightly decreased to a minimal value with Ag doping, and was found to be about 3.65 eV for R{sub Ag

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.

Effect of Ag additions on the lengthening rate of Ω plates and formation of σ phase in Al-Cu-Mg alloys during thermal exposure

Energy Technology Data Exchange (ETDEWEB)

Zhou, Yaru; Liu, Zhiyi, E-mail: liuzhiyi@csu.edu.cn; Bai, Song; Ying, Puyou; Lin, Lianghua

2017-01-15

Effect of Ag additions on the mechanical properties and microstructures of the peak-aged Al-Cu-Mg alloys during prolonged thermal exposure at 150 °C, was investigated by tensile testing, conventional transmission electron microscopy (TEM) and scanning transmission electron microscopy (STEM). The results showed that after exposure for 500 h, > 85% of the peak strength remained. Microstructure observations indicated that increasing the Ag content from 0.14 to 0.57% promoted the precipitation of a fine and uniform Ω phase and suppressed the formation of the θ′ phase, leading to a notable improvement of the strength properties and thermal stability of the studied alloys. Quantitative TEM analysis showed that the coarsening of Ω phase was predominated by plate lengthening rather than thickening, while its lengthening rate was independent of various Ag additions during exposure at 150 °C. In addition, an increase of Ag also facilitated the formation of a cubic σ phase, which was further supported by STEM results. - Highlights: •Increasing Ag improved strength properties and thermal stability of the alloys. •After exposure for 500 h, > 85% of the peak strength remained. •The lengthening rate of Ω plates remained constant as Ag increased at 150 °C. •Increasing Ag content facilitated the formation of σ phase.

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)

Near-surface and bulk behavior of Ag in SiC

International Nuclear Information System (INIS)

Xiao, H.Y.; Zhang, Y.; Snead, L.L.; Shutthanandan, V.; Xue, H.Z.; Weber, W.J.

2012-01-01

Highlights: ► Ag release from SiC poses problems in safe operation of nuclear reactors. ► Near-surface and bulk behavior of Ag are studied by ab initio and ion beam methods. ► Ag prefers to adsorb on the surface rather than in the bulk SiC. ► At high temperature Ag desorbs from the surface instead of diffusion into bulk SiC. ► Surface diffusion may be a dominating mechanism accounting for Ag release from SiC. - Abstract: The diffusive release of fission products, such as Ag, from TRISO particles at high temperatures has raised concerns regarding safe and economic operation of advanced nuclear reactors. Understanding the mechanisms of Ag diffusion is thus of crucial importance for effective retention of fission products. Two mechanisms, i.e., grain boundary diffusion and vapor or surface diffusion through macroscopic structures such as nano-pores or nano-cracks, remain in debate. In the present work, an integrated computational and experimental study of the near-surface and bulk behavior of Ag in silicon carbide (SiC) has been carried out. The ab initio calculations show that Ag prefers to adsorb on the SiC surface rather than in the bulk, and the mobility of Ag on the surface is high. The energy barrier for Ag desorption from the surface is calculated to be 0.85–1.68 eV, and Ag migration into bulk SiC through equilibrium diffusion process is not favorable. Experimentally, Ag ions are implanted into SiC to produce Ag profiles buried in the bulk and peaked at the surface. High-temperature annealing leads to Ag release from the surface region instead of diffusion into the interior of SiC. It is suggested that surface diffusion through mechanical structural imperfection, such as vapor transport through cracks in SiC coatings, may be a dominating mechanism accounting for Ag release from the SiC in the nuclear reactor.

Studies on highly luminescent AgInS{sub 2} and Ag–Zn–In–S quantum dots

Energy Technology Data Exchange (ETDEWEB)

Xiang, Weidong, E-mail: xiangweidong001@126.com [College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035 (China); College of Materials Science and Engineering, Tongji University, Shanghai 201804 (China); Xie, Cuiping; Wang, Jing; Zhong, Jiasong; Liang, Xiaojuan; Yang, Hailong; Luo, Le [College of Materials Science and Engineering, Tongji University, Shanghai 201804 (China); Chen, Zhaoping [College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035 (China)

2014-03-05

Highlights: • The quantum yield of the obtained ternary AgInS{sub 2} QDs was up to 62% with the emission peak of 642 nm under the excitation of 460 nm. • Colorful luminescent Ag–Zn–In–S QDs were obtained by adding Zn salts directly as well as Ag and In precursors. • The obtained highly luminescent quantum dots showed promising applications in the white light emitting diodes (W-LED). • The electroluminescence (EL) of AgInS{sub 2} QDs was observed in QD-LED device. -- Abstract: Silver indium sulfide (AIS) quantum dots (QDs) with different Ag/In molar ratios were synthesized via a hot-injection method. Intense photoluminescence (PL) originating from the donor–acceptor pair recombination were observed for all the samples and the emission peak blue-shifted from 739 to 632 nm, being similar to the behavior of the absorption onset as the Ag/In ratios decreased. The highest PL quantum yield (QY) of the obtained ternary AIS QDs was ca. 62% with an optimum ratio of Ag/In = 1/4. Compared with AIS QDs, when Zn ions were introduced, the absorption spectra of the obtained quaternary Ag–Zn–In–S QDs were blue-shifted, and their emission peaks moved to higher energies accordingly, showing a tunable emission from red to green by altering the band gap energy. In order to further study the electroluminescence (EL) as well as looking forward to the applications in the optoelectronic devices of the obtained highly luminescent nanoparticles, the colloidal AIS QDs were deposited as thin films to the sandwich-like structured QD-LED. The experimental results showed that the obtained EL device exhibited EL emission originated from QDs thin films by adjusting the turn on voltage, which is for the first time to realize EL of AIS QDs in such QD-LED.

The Disappearing Forests. UNEP Environment Brief No. 3.

Science.gov (United States)

United Nations Environment Programme, Nairobi (Kenya).

Tropical forests cover 20 percent of the Earth's land surface, but they are rapidly disappearing, with some estimating the loss of 7.5 million hectares a year. This bulletin provides a set of key facts relating to this problem. It details: (1) factors involving the rate at which the forests are disappearing; (2) some of the effects of these losses…

Synthesis and Property of Ag(NP)/catechin/Gelatin Nanofiber

Science.gov (United States)

Nasir, Muhamad; Apriani, Dita

2017-12-01

Nanomaterial play important role future industry such as for the medical, food, pharmaceutical and cosmetic industry. Ag (NP) and catechin exhibit antibacterial property. Ag(NP) with diameter around 15 nm was synthesis by microwaved method. We have successfully produce Ag(NP)/catechin/gelatin nanofiber composite by electrospinning process. Ag(NP)/catechin/gelatin nanofiber was synthesized by using gelatin from tuna fish, polyethylene oxide (PEO), acetic acid as solvent and silver nanoparticle(NP)/catechin as bioactive component, respectively. Morphology and structure of bioactive catechin-gelatin nanofiber were characterized by scanning electron microscopy (SEM) and fourier transform infrared spectroscopy (FTIR), respectively. SEM analysis showed that morphology of nanofiber composite was smooth and had average diameter 398.97 nm. FTIR analysis results were used to confirm structure of catechin-gelatin nanofiber. It was confirmed by FTIR that specific vibration band peak amide A (N-H) at 3286,209 cm-1, amide B (N-H) 3069,396 cm-1, amide I (C=O) at 1643,813 cm-1, amide II (N-H and CN) at 1538,949 cm-1, amide III (C-N) at 1276,789 cm-1, C-O-C from polyethylene oxide at 1146,418 cm-1, respectively. When examined to S. Aureus bacteria, Ag/catechin/gelatin nanofiber show inhabitation performance around 40.44%. Ag(NP)/catechin/gelatin nanofiber has potential application antibacterial medical application.

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).

Photocatalytic properties of nanocrystalline TiO2 thin film with Ag additions

International Nuclear Information System (INIS)

Chang, C.-C.; Lin, C.-K.; Chan, C.-C.; Hsu, C.-S.; Chen, C.-Y.

2006-01-01

In the present study, nanocrystalline TiO 2 /Ag composite thin films were prepared by a sol-gel spin coating technique. While, by introducing polystyrene (PS) microspheres, porous TiO 2 /Ag films were obtained after calcining at a temperature of 500 o C. The as-prepared TiO 2 and TiO 2 /Ag thin films were characterized by X-ray diffractometry, and scanning electron microscopy to reveal the structural and morphological differences. In addition, the photocatalytic properties of these films were investigated by degrading methylene blue under UV irradiation. After 500 o C calcination, the microstructure of PS-TiO 2 film without Ag addition exhibited a sponge-like microstructure while significant sintering effect was noticed with Ag additions and the films exhibited a porous microstructure. Meanwhile, coalescence of nanocrystalline anatase-phase TiO 2 can be observed with respect to the sharpening of XRD diffraction peaks. The photodegradation of porous TiO 2 doped with 1 mol% Ag exhibited the best photocatalytic efficiency where 72% methylene blue can be decomposed after UV exposure for 12 h

Anomalous growth of Ba on Ag(111)

International Nuclear Information System (INIS)

Teodoro, O.M.N.D.; Los, J.; Moutinho, A.M.C.

2002-01-01

Electropositive elements are often adsorbed on metals to produce a well-known decrease in the surface work function. During deposition, the work function drops steeply and reaches a minimum at coverage lower than one monolayer. Then, it increases slightly and the work function converges to the value of the deposited element. In this work, we report anomalous behavior found during the deposition of barium on a Ag(111) surface. After a minimum of about 2.4 eV the work function did not increase up to 2.7 eV, the bulk barium work function, no matter what amount of barium was deposited. Auger electron spectroscopy corroborated these results in which we measured a permanent and constant intensity of the Ag MNN peak for high barium coverage. To explain this anomalous growth of barium on Ag(111) we propose an explanation based on the diffusion of silver atoms into the barium film. Further experiments showed that coadsorption of oxygen before a second deposition of barium blocked the diffusion thus allowing the work function to reach 2.7 eV

Effect of annealing temperature and dopant concentration on the thermoluminescence sensitivity in LiF:Mg,Cu,Ag material.

Science.gov (United States)

Yahyaabadi, Akram; Torkzadeh, Falamarz; Rezaei Ochbelagh, Dariush; Hosseini Pooya, Seyed Mahdi

2018-04-24

LiF:Mg,Cu,Ag is a new dosimetry material that is similar to LiF:Mg,Cu,P in terms of dosimetric properties. The effect of the annealing temperature in the range of 200 to 350°C on the thermoluminescence (TL) sensitivity and the glow curve structure of this material at different concentrations of silver (Ag) was investigated. It has been demonstrated that the optimum values of the annealing temperature and the Ag concentration are 240°C and 0.1 mol% for better sensitivity, respectively. The TL intensity decreases at annealing temperatures lower than 240°C or higher than 240°C, reaching a minimum at 300°C and then again increases for various Ag concentrations. It was observed that the glow curve structure altered and the area under the low temperature peak as well as the area under the main dosimetric peak decreased with increasing annealing temperature. The position of the main dosimetric peak moved in the direction of higher temperatures, but at 320 and 350°C annealing temperatures, it shifted to lower temperatures. It was also observed that the TL sensitivity could partially be recovered by a combined annealing procedure. Copyright © 2018 John Wiley & Sons, Ltd.

Visible light driven photocatalysis and antibacterial activity of AgVO3 and Ag/AgVO3 nanowires

International Nuclear Information System (INIS)

Singh, Anamika; Dutta, Dimple P.; Ballal, A.; Tyagi, A.K.; Fulekar, M.H.

2014-01-01

Graphical abstract: - Highlights: • Ag/AgVO 3 and pure AgVO 3 nanowires synthesized by sonochemical process. • Characterization done using XRD, SEM, TEM, EDX and BET analysis. • Visible light degradation of RhB by Ag/AgVO 3 within 45 min. • Antibacterial activity of Ag/AgVO 3 demonstrated. - Abstract: Ag/AgVO 3 nanowires and AgVO 3 nanorods were synthesized in aqueous media via a facile sonochemical route. The as-synthesized products were characterized by X-ray diffraction, Brunauer–Emmett–Teller surface area analysis, scanning electron microscopy together with an energy dispersion X-ray spectrum analysis, transmission electron microscopy and UV–vis diffuse reflectance spectroscopy. The results revealed that inert atmosphere promotes the formation of Ag/AgVO 3 nanowires. The photocatalytic studies revealed that the Ag/AgVO 3 nanowires exhibited complete photocatalytic degradation of Rhodamine B within 45 min under visible light irradiation. The antibacterial activity of Ag/AgVO 3 nanowires was tested against Escherechia coli and Bacillus subtilis. The minimum growth inhibitory concentration value was found to be 50 and 10 folds lower than for the antibiotic ciprofloxacin for E. coli and B. subtilis, respectively. The antibacterial properties of the β-AgVO 3 nanorods prove that in case of the Ag dispersed Ag/AgVO 3 nanowires, the enhanced antibacterial action is also due to contribution from the AgVO 3 support

Optical properties tailoring by high fluence implantation of Ag ions on sapphire

International Nuclear Information System (INIS)

Marques, C.; Silva, R.C. da; Wemans, A.; Maneira, M.J.P.; Kozanecki, A.; Alves, E.

2006-01-01

Optical and structural properties of single crystalline α-Al 2 O 3 were changed by the implantation of high fluences of Ag ions. Colourless transparent (101-bar 0) sapphire samples were implanted at room temperature with 160keV silver ions and fluences up to 1x10 17 Agcm -2 . Surface amorphization is observed at the fluence of 6x10 16 Agcm -2 . Except for the lower fluences (below 6x10 16 Agcm -2 ) the optical absorption spectra reveal the presence of a band peaking in the region 450-500nm, depending on the retained fluence. This band has been attributed to the presence of silver colloids, being thus 1x10 16 Agcm -2 below the threshold for colloid formation during the implantation. Annealing in oxidizing atmosphere promotes the recrystallization along with segregation of Ag followed by loss through evaporation. Recrystallization is retarded for annealing in reducing atmosphere and the Ag profile displays now a double peak structure after evaporation. Playing with the implantation fluence, temperature and annealing atmosphere controllable shifts of the position and intensity of the optical bands in the visible were achieved

Effect of Ag doping on the properties of ZnO thin films for UV stimulated emission

Science.gov (United States)

Razeen, Ahmed S.; Gadallah, A.-S.; El-Nahass, M. M.

2018-06-01

Ag doped ZnO thin films have been prepared using sol-gel spin coating method, with different doping concentrations. Structural and morphological properties of the films have been investigated by X-ray diffraction (XRD) and scanning electron microscopy (SEM) techniques. Thin films have been optically pumped and stimulated emission has been observed with strong peaks in the UV region. The UV stimulated emission is found to be due to exciton-exciton scattering, and Ag doping promoted this process by increasing the excitons concentrations in the ZnO lattice. Output-input intensity relation and peak emission, FWHM, and quantum efficiency relations with pump intensity have been reported. The threshold for which stimulated emission started has been evaluated to be about 18 MW/cm2 with quantum efficiency of about 58.7%. Mechanisms explaining the role of Ag in enhancement of stimulated emission from ZnO thin films have been proposed.

Photocatalytic performance of graphene/TiO_2-Ag composites on amaranth dye degradation

International Nuclear Information System (INIS)

Roşu, Marcela-Corina; Socaci, Crina; Floare-Avram, Veronica; Borodi, Gheorghe; Pogăcean, Florina; Coroş, Maria; Măgeruşan, Lidia; Pruneanu, Stela

2016-01-01

Ternary nanocomposites containing TiO_2, silver and graphene with different reduction levels were prepared and used as photocatalysts for amaranth azo dye degradation, under UV and natural light exposure. The obtained materials were characterized by TEM, XRD, FTIR and UV-Vis spectroscopy, confirming the successful formation of the nanocomposites. HPLC analysis along with UV-Vis spectroscopy were employed to quantify the concentration of non-degraded dye in solution. The graphene/TiO_2-Ag nanocomposites proved to have remarkable photocatalytic activities for amaranth degradation under UV and solar irradiation (85.3–98% of dye has disappeared in the first 2 h). Also, significant removal efficiencies (between 40.5 and 71.8%) of photocatalysts, in day light conditions, were demonstrated. The best result for amaranth dye degradation was obtained with the reduced graphene/TiO_2-Ag catalyst (up to 99.9%). Based on the degradation products analysis, a photodegradation pathway of amaranth dye was also proposed. - Highlights: • Graphene/TiO_2-Ag composites were prepared by a combined chemical-thermal method. • The composites showed improved light-absorption characteristics. • A significant degradation performance of amaranth was obtained with these composites under UV and natural light exposure. • Graphene/TiO_2-Ag composites offer a high potential for various photocatalytic applications in pollutant removal processes.

Facile biosynthesis of Ag-NPs using Otostegia limbata plant extract: Physical characterization and auspicious biological activities

Directory of Open Access Journals (Sweden)

Rizwan Kausar

2016-09-01

Full Text Available Silver nanoparticles (Ag-NPs synthesized through reduction by Otostegia limbata green extract are, hereby, reported for the first time. It is very interesting to observe that in this case, O. limbata plant extract acts as a strong chelating agent in Ag-NPs formation through AgNO3. Scanning electron microscope (SEM studies expose that Ag-NPs formation is highly homogenous and spherical with mean particle size of 32±0.8 nm. A typical Ag absorption peak has been observed at 419 nm by ultra violet (UV-visible spectroscopy which have endorsed the successful formation of single phase Ag-NPs. X-ray diffraction (XRD and Fourier transform infrared spectroscopy (FTIR examination further validates the crystalline pure phase structure of Ag-NPs. Promising results have been recorded against protein kinase inhibition assay and antibacterial assay having prominent pathogenic strains. Our present study explores that biosynthesized eco-friendly Ag-NPs have great potential, in the future, for anticancer drug development with wide range pharmaceutical applications.

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)

Preparation and antibacterial activities of Ag/Ag+/Ag3+ nanoparticle composites made by pomegranate (Punica granatum rind extract

Directory of Open Access Journals (Sweden)

Hui Yang

Full Text Available Nano-silver and its composite materials are widely used in medicine, food and other industries due to their strong conductivity, size effect and other special performances. So far, more microbial researches have been applied, but a plant method is rarely reported. In order to open up a new way to prepare AgNP composites, pomegranate peel extract was used in this work to reduce Ag+ to prepare Ag/Ag+/Ag3+ nanoparticle composites. UV–Vis was employed to detect and track the reduction of Ag+ and the forming process of AgNPs. The composition, structure and size of the crystal were analyzed by XRD and TEM. Results showed that, under mild conditions, pomegranate peel extract reacted with dilute AgNO3 solution to produce Ag/Ag+/Ag3+ nanoparticle composites. At pH = 8 and 10 mmol/L of AgNO3 concentration, the size of the achieved composites ranged between 15 and 35 nm with spherical shapes and good crystallinity. The bactericidal experiment indicated that the prepared Ag/Ag+/Ag3+ nanoparticles had strong antibacterial activity against gram positive bacteria and gram negative bacteria. FTIR analysis revealed that biological macromolecules with groups of NH2, OH, and others were distributed on the surface of the newly synthesized Ag/Ag+/Ag3+ nanoparticles. This provided a useful clue to further study the AgNP biosynthesis mechanism. Keywords: Pomegranate rind, Biosynthesis, Ag/Ag+/Ag3+ nanoparticle composites, Antibacterial activity

On-the-fly green generation and dispersion of AgI nanoparticles for cloud seeding nuclei

Energy Technology Data Exchange (ETDEWEB)

Hu, Xiuli; Zhou, Wenbo; Wang, Xizheng; Wu, Tao; Delisio, Jeffery B.; Zachariah, Michael R., E-mail: mrz@umd.edu [University of Maryland, Department of Chemical and Biomolecular Engineering (United States)

2016-07-15

This study reports on an on-the-fly green synthesis/dispersion of silver iodide (AgI) nanoparticles from the combustion of AgIO{sub 3}/carbon black (CB)/nitrocellulose (NC) composites, which could be used as a candidate for a cloud-seeding pyrotechnic. Films were formed by direct electrospray deposition of a mixture of synthesized silver iodate with CB and NC. The decomposition pathways of AgIO{sub 3}/CB and AgIO{sub 3}/CB/NC were evaluated by temperature jump time of flight mass spectrometry (T-jump TOFMS) and XRD, showing that AgI particles and CO{sub 2} are released from the reaction between AgIO{sub 3} and CB without other toxic residuals. The flame propagation velocity of AgIO{sub 3}/CB/NC films increases with the increasing of particle mass loading of AgIO{sub 3} and CB and peaks at 40 wt%, which is much higher than that of an AgI/AP/NC film. The mean diameter of the resultant AgI nanoparticles is from 51 to 97 nm. The mass loading of AgIO{sub 3} and CB was found to play a major role in size control of the AgI nanoparticles.

The role of Ag precipitates in Cu-12 wt% Ag

Energy Technology Data Exchange (ETDEWEB)

Yao, D.W.; Song, L.N. [Department of Materials Science and Engineering, Zhejiang University, Zheda Road No.38, Hangzhou, Zhejiang 310027 (China); Dong, A.P.; Wang, L.T. [China Railway Construction Electrification Bureau Group Co.,Ltd., Beijing 100036 (China); Zhang, L. [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Meng, L., E-mail: mengliang@zju.edu.cn [Department of Materials Science and Engineering, Zhejiang University, Zheda Road No.38, Hangzhou, Zhejiang 310027 (China)

2012-12-15

The Cu-12 wt% Ag was prepared to investigate the role of Ag precipitates on the properties of the alloy. Two kinds of heat treatment procedures were adopted to produce different amount of Ag precipitates in the Cu-12 wt% Ag. The microstructure of Ag precipitates was systematically observed by optical microscopy and electron microscopy. The Cu-12 wt% Ag with more Ag precipitates exhibits higher strength and lower electrical conductivity. More Ag precipitates results in more phase interface and less Ag atoms dissolved in Cu matrix. By comparing the strengthening effect and electron scattering effect of phase interface and dissolved Ag atoms, it is conclude that the interface between Cu matrix and Ag precipitates could significantly block dislocation movement and enhance electron scattering in Cu-Ag alloys.

An overview of Booster and AGS Polarized Proton Operations during Run 17

Energy Technology Data Exchange (ETDEWEB)

Zeno, K. [Brookhaven National Lab. (BNL), Upton, NY (United States)

2017-10-11

There were only a few differences in the setup between this year’s Polarized Proton run and the previous one (Run 15). Consequently, this note will focus on these differences as well as a few more notable studies done during the course of the run. This year, the Booster input intensity was kept around 7e11 for the majority of the run whereas in Run 15 it was kept around 9e11. It was lowered because there was some indication that the source polarization was higher with this lower input. Some of the polarization measurements that motivated this change will be discussed. Both the emittance and polarization on the AGS flattop show intensity dependence, thought to be related to the peak current, especially early in the AGS acceleration ramp. In Run 15, the AGS Rf was configured for h=8, but in this run h=6 was used to reduce the peak current and also to allow for the possibility of using a dual harmonic to reduce it further. Eventually, a dual harmonic configuration was used for the first 100 ms or so of the AGS acceleration cycle. Two cavities were set to h=12 and phased differently than the other 8 to accomplish this. Quad pumping was also used at Booster extraction to make the bunch injected into the AGS wider in order to match the dual harmonic bucket right at injection. This configuration, which was used for the majority of the run, will be described. Measurements of the intensity dependence of the transverse emittance and polarization with and without it will be compared.

Synthesis and characterization of Ag nanowires: Improved performance in dye sensitized solar cells

Directory of Open Access Journals (Sweden)

Safia A. Kazmi

2016-09-01

Full Text Available Development of highly efficient dye-sensitized solar cells (DSSCs with good photovoltaic parameters is an active research area of current global interest. Recently, one dimensional nanomaterial, such as nanorods and nanotubes has replaced the nanoparticles used in DSSCs anode because of their ability to improve the electron transport leading to enhanced electron collection efficiency. In the present work, rapid synthesis of silver nanowires (AgNWs was done. The XRD characterization was performed to confirm the formation and size of synthesized AgNWs. It was observed that FWHM of the diffraction peaks was increased with AgNWs concentration in TiO2. The synthesized TiO2AgNWs nanocomposite was used as the photo anode of Dye sensitized solar cell. The I–V characteristics of the solar cell were drawn using standard conditions. It was observed that TiO2AgNWs based solar cells have significantly increased photocurrent density resulting in improved conversion efficiency as compared to pure TiO2 based DSSC.

Preparation and antibacterial activities of Ag/Ag+/Ag3+ nanoparticle composites made by pomegranate (Punica granatum) rind extract

Science.gov (United States)

Yang, Hui; Ren, Yan-yu; Wang, Tao; Wang, Chuang

Nano-silver and its composite materials are widely used in medicine, food and other industries due to their strong conductivity, size effect and other special performances. So far, more microbial researches have been applied, but a plant method is rarely reported. In order to open up a new way to prepare AgNP composites, pomegranate peel extract was used in this work to reduce Ag+ to prepare Ag/Ag+/Ag3+ nanoparticle composites. UV-Vis was employed to detect and track the reduction of Ag+ and the forming process of AgNPs. The composition, structure and size of the crystal were analyzed by XRD and TEM. Results showed that, under mild conditions, pomegranate peel extract reacted with dilute AgNO3 solution to produce Ag/Ag+/Ag3+ nanoparticle composites. At pH = 8 and 10 mmol/L of AgNO3 concentration, the size of the achieved composites ranged between 15 and 35 nm with spherical shapes and good crystallinity. The bactericidal experiment indicated that the prepared Ag/Ag+/Ag3+ nanoparticles had strong antibacterial activity against gram positive bacteria and gram negative bacteria. FTIR analysis revealed that biological macromolecules with groups of sbnd NH2, sbnd OH, and others were distributed on the surface of the newly synthesized Ag/Ag+/Ag3+ nanoparticles. This provided a useful clue to further study the AgNP biosynthesis mechanism.

Plasmonic Ag{sub 2}MoO{sub 4}/AgBr/Ag composite: Excellent photocatalytic performance and possible photocatalytic mechanism

Energy Technology Data Exchange (ETDEWEB)

Wang, Zhongliao [College of Physics and Electronic Information, Anhui Key Laboratory of Energetic Materials, Huaibei Normal University, Huaibei, 235000 (China); Zhang, Jinfeng, E-mail: zjf_y2004@126.com [College of Physics and Electronic Information, Anhui Key Laboratory of Energetic Materials, Huaibei Normal University, Huaibei, 235000 (China); Lv, Jiali [College of Physics and Electronic Information, Anhui Key Laboratory of Energetic Materials, Huaibei Normal University, Huaibei, 235000 (China); Dai, Kai, E-mail: daikai940@chnu.edu.cn [College of Physics and Electronic Information, Anhui Key Laboratory of Energetic Materials, Huaibei Normal University, Huaibei, 235000 (China); Liang, Changhao [College of Physics and Electronic Information, Anhui Key Laboratory of Energetic Materials, Huaibei Normal University, Huaibei, 235000 (China); Key Laboratory of Materials Physics and Anhui Key Laboratory of Nanomaterials and Nanotechnology, Institute of Solid State Physics, Chinese Academy of Sciences, Hefei, 230031 (China)

2017-02-28

Highlights: • Novel Ag{sub 2}MoO{sub 4}/AgBr/Ag photocatalyst was prepared. • Ag{sub 2}MoO{sub 4}/AgBr/Ag showed high photocatalytic activity. • Ag{sub 2}MoO{sub 4}/AgBr/Ag showed long reusable life. - Abstract: Plasmonic Ag{sub 2}MoO{sub 4}/AgBr/Ag composite is fabricated by in-situ ion exchange and reduction methods at room temperature. The samples are characterized by X-ray diffraction (XRD), UV–vis diffuse reflectance (DRS), energy-dispersive X-ray spectroscopy (EDS), scanning electron microscope (SEM) and photoluminescence (PL) measurements. The results show that butterfly-like Ag{sub 2}MoO{sub 4} nanosheets served as the precursor, and Ag{sub 2}MoO{sub 4}/AgBr/Ag is formed in phase transformation with MoO{sub 4}{sup 2−} displaced by Br{sup −}. The ternary Ag{sub 2}MoO{sub 4}/AgBr/Ag composite photocatalysts show greatly enhanced photocatalytic activity in photodegrading methylene blue (MB) under visible light irradiation compared with AgBr and Ag{sub 2}MoO{sub 4}. The pseudo-first-order rate constant k{sub app} of Ag{sub 2}MoO{sub 4}/AgBr/Ag is 0.602 min{sup −1}, which is 11.6 and 18.3 times as high as that of AgBr and Ag{sub 2}MoO{sub 4}, respectively. Meanwhile, the efficiency of degradation still kept 90% after ten times cyclic experiments. Eventually, possible photocatalytic mechanism was proposed.

Intermediate-range chemical ordering of cations in molten RbCl-AgCl

Energy Technology Data Exchange (ETDEWEB)

Tahara, S. [Department of Physics and Earth Sciences, Faculty of Science, University of the Ryukyus, Okinawa 903-0213 (Japan); Research and Utilization Division, Japan Synchrotron Radiation Research Institute (JASRI, SPring-8), Hyogo 679-5198 (Japan); Kawakita, Y. [J-PARC Center, Japan Atomic Energy Agency (JAEA), Ibaraki 319-1195 (Japan); Shimakura, H. [Faculty of Pharmacy, Niigata University of Pharmacy and Applied Life Sciences, Niigata 956-8603 (Japan); Ohara, K. [Research and Utilization Division, Japan Synchrotron Radiation Research Institute (JASRI, SPring-8), Hyogo 679-5198 (Japan); Fukami, T. [Department of Physics and Earth Sciences, Faculty of Science, University of the Ryukyus, Okinawa 903-0213 (Japan); Takeda, S. [Department of Physics, Faculty of Sciences, Kyushu University, Fukuoka 812-8581 (Japan)

2015-07-28

A first sharp diffraction peak (FSDP) is observed in the X-ray total structure factor of a molten mixture of RbCl-AgCl, while both pure melts of RbCl and AgCl do not exhibit FSDP individually. Molecular dynamics simulations were performed to investigate the origin of the FSDP with the polarizable ion model (PIM). Coexistence of covalent Ag–Cl and ionic Rb–Cl bonds leads the system to evolve intermediate range ordering, which is simulated by introducing the induced polarization in different ways between Ag–Cl with fully polarizable treatment based on Vashishta-Raman potential and Rb–Cl with suppression over-polarization in the nearest neighbor contribution based on Born-Meyer potential. The partial structure factors for both the Ag–Ag and Rb–Rb correlations, S{sub AgAg}(Q) and S{sub RbRb}(Q), show a positive contribution to the FSDP, while S{sub AgRb}(Q) for the Ag–Rb correlation exhibits a negative contribution, indicating that Ag and Rb ions are distributed in an alternating manner within the intermediate-range length scale. The origin of the intermediate-range chemical ordering of cations can be ascribed to the preferred direction of the dipole moments of anions in the PIM.

Intermediate-range chemical ordering of cations in molten RbCl-AgCl

International Nuclear Information System (INIS)

Tahara, S.; Kawakita, Y.; Shimakura, H.; Ohara, K.; Fukami, T.; Takeda, S.

2015-01-01

A first sharp diffraction peak (FSDP) is observed in the X-ray total structure factor of a molten mixture of RbCl-AgCl, while both pure melts of RbCl and AgCl do not exhibit FSDP individually. Molecular dynamics simulations were performed to investigate the origin of the FSDP with the polarizable ion model (PIM). Coexistence of covalent Ag–Cl and ionic Rb–Cl bonds leads the system to evolve intermediate range ordering, which is simulated by introducing the induced polarization in different ways between Ag–Cl with fully polarizable treatment based on Vashishta-Raman potential and Rb–Cl with suppression over-polarization in the nearest neighbor contribution based on Born-Meyer potential. The partial structure factors for both the Ag–Ag and Rb–Rb correlations, S AgAg (Q) and S RbRb (Q), show a positive contribution to the FSDP, while S AgRb (Q) for the Ag–Rb correlation exhibits a negative contribution, indicating that Ag and Rb ions are distributed in an alternating manner within the intermediate-range length scale. The origin of the intermediate-range chemical ordering of cations can be ascribed to the preferred direction of the dipole moments of anions in the PIM

Using 13X, LiX, and LiPdAgX zeolites for CO_2 capture from post-combustion flue gas

International Nuclear Information System (INIS)

Chen, S.J.; Zhu, M.; Fu, Y.; Huang, Y.X.; Tao, Z.C.; Li, W.L.

2017-01-01

Highlights: • We synthesized a novel adsorbent named LiPdAgX zeolite. • CCS was proposed from microstructure, selectivity and separation factor of zeolite. • The static and flowing adsorption using CO_2/N_2 mixture on X zeolites were studied. • LiPdAgX zeolite required less energy for regeneration compared to 13X and MEA. • LiPdAgX zeolite can effectively capture CO_2 from post-combustion flue gas. - Abstract: This work investigates the application of X zeolites for capturing CO_2 from post-combustion flue gas. LiX and LiPdAgX zeolites were prepared by an ion-exchange method using 13X zeolite. X-ray diffraction analysis showed that all samples exhibited characteristic peaks of X zeolites, where the peak intensities increased in the order: LiPdAgX > LiX > 13X. The enhanced intensity of the diffraction peaks can increase the activity of the X zeolites and improve their adsorption performance. Scanning electron microscopy imaging showed that the intergranular pore canals of LiPdAgX zeolite were more concentrated. Pore structure analysis indicated that addition of Li"+ to the 13X zeolite enhanced the specific surface areas and pore volumes of the zeolites. Among the 13X, LiX, and LiPdAgX zeolites, LiPdAgX showed the highest CO_2/N_2selectivity, where the difference in the CO_2 adsorption capacity was due to differences in the number of adsorption sites and thermal conductivities of the X zeolites. The CO_2 breakthrough time increased in succession for the 13X, LiX, and LiPdAgX zeolites. The CO_2/N_2 separation factor of the LiPdAgX zeolite was twice that of the 13X zeolite at a CO_2 concentration of 20 vol.%. The temperature variations during the adsorption process were used to determine the regeneration energy and adsorption capacity of the X zeolites. LiPdAgX zeolite required less energy for regeneration than 13X zeolite and MEA. After regeneration, the separation factor of LiPdAgX zeolite remained at 6.38 for 20 vol.% CO_2 in the flue gas. Therefore, LiPdAg

An approach for scalable production of silver (Ag) decorated WS2 nanosheets

Science.gov (United States)

Sumesh, C. K.; Kapatel, Sanni; Chaudhari, Arti

2018-05-01

In the Present study we report the synthesis of Ag nanoparticles (NPs) decorated WS2 nanosheets by sonochemical exfoliation followed by simple chemical reduction process at room temperature. The morphology and microstructure of the as-synthesized Ag-WS2 nanocomposite were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and optical absorption (UV-Vis.) spectroscopy. X-ray and TEM analysis shows the presence of Ag with significant peak over 38.08°, 44.22°, 64.37° and 77.33° at 2θ angle for (111), (200), (220) and (311) respectively. The Ag nanoparticles are randomly distributed throughout the surface of the WS2 nanosheets without undergoing further oxidation during the formation of composites. The formation of Ag-WS2 nanocomposites shows a clear blue shift in the absorption as we obtained the characteristics absorption valleys at 456, 536 and 631 nm from the UV Vis spectroscopy analysis compared to pure WS2 nanosheets. Henceforth a facile method for the Ag decoration on WS2 nanosheets was put forward and briefly discussed. The proposed synthesis method is very promising for the low cost and large-scale synthesis of other noble metal incorporation TMDC compounds.

Electronic structure of Co islands grown on the {radical}3 x {radical}3-Ag/Ge(111) surface

Energy Technology Data Exchange (ETDEWEB)

Huang, Xiao-Lan; Chou, Chi-Hao; Lin, Chun-Liang; Tomaszewska, Agnieszka; Fu, Tsu-Yi, E-mail: phtifu@phy.ntnu.edu.tw

2011-09-30

By means of room temperature scanning tunneling spectroscopy (RT STS), we have studied the electronic structure of two different Ag/Ge(111) phases as well as Co islands grown on the {radical}3 x {radical}3-Ag/Ge (111) forming either {radical}13 x {radical}13 or 2 x 2 patterns. The spectrum obtained from 4 x 4-Ag/Ge(111) structure shows the existence of a shoulder at 0.7 V which is also present in the electronic structure of the Ge(111)-c2 x 8 and indicates donation of Ge electrons to electronic states of the Ag-driven phase. However, this fact is not supported by the electronic spectrum taken from the {radical}3 x {radical}3-Ag/Ge (111). The complexity of the Co-{radical}13 x {radical}13 islands bonding with the substrate is mirrored by a large number of peaks in their electronic spectra. The spectra obtained from the Co-2 x 2 islands which had grown on the step differ from those taken from Co-2 x 2 islands located along the edge of the terrace by a number of peaks at negative sample bias. This discrepancy is elucidated in terms of dissimilarities of Co-substrate interaction accompanying Co islands growth on different areas of the stepped surface.

Controllable synthesis of dual emissive Ag:InP/ZnS quantum dots with high fluorescence quantum yield

Science.gov (United States)

Yang, Wu; He, Guoxing; Mei, Shiliang; Zhu, Jiatao; Zhang, Wanlu; Chen, Qiuhang; Zhang, Guilin; Guo, Ruiqian

2017-11-01

Dual emissive Cd-free quantum dots (QDs) are in great demand for various applications. However, their synthesis has been faced with challenges. Here, we demonstrate the dual emissive Ag:InP/ZnS core/shell QDs with the excellent photoluminescence quantum yield (PL QY) up to 75% and their PL dependence on the reaction temperature, reaction time, the different ZnX2 (X = I, Cl, and Br) precursors, the ratio of In/Zn and the Ag dopant concentration. The as-prepared Ag:InP/ZnS QDs exhibit dual emission with one peak position of about 492 nm owing to the intrinsic emission, and the other peak position of about 575 nm resulting from Ag-doped emission. These dual emissive QDs are integrated with the commercial GaN-based blue LEDs, and the simulation results show that the Ag:InP/ZnS QDs-based white LEDs could realize bright natural white-lights with the luminous efficacy (LE) of 94.2-98.4 lm/W, the color rendering index (CRI) of 82-83 and the color quality scale (CQS) of 82-83 at different correlated color temperatures (CCT). This unique combination of the above properties makes this new class of dual emissive QDs attractive for white LED applications.

Ag K- and L3-edge XAFS study on Ag species in Ag/Ga2O3 photocatalysts

International Nuclear Information System (INIS)

Yamamoto, M; Yamamoto, N; Yoshida, T; Nomoto, T; Yamamoto, A; Yoshida, H; Yagi, S

2016-01-01

Ag loaded Ga 2 O 3 (Ag/Ga 2 O 3 ) shows photocatalytic activity for reduction of CO 2 with water. Ag L 3 -edge XANES and K-edge EXAFS spectra were measured for various Ag/Ga 2 O 3 samples, which suggested that structural and chemical states of Ag species varied with the loading amount of Ag and the preparation method. The Ag species were metallic Ag particles with an AgGaO 2 -like interface structure in the sample with high loading amount of Ag while predominantly Ag metal clusters in the sample with low loading amount of Ag. The XANES feature just above the edge represented the interaction between the Ag species and the Ga 2 O 3 surface, showing that the Ag metal clusters had more electrons in the d -orbitals by interacting with the Ga 2 O 3 surface, which would contribute the high photocatalytic activity. (paper)

Disappearance of neutron magic numbers and deformation coexistence

International Nuclear Information System (INIS)

Kimura, Masaaki

2014-01-01

The disappearance of N=8, 20 and 28 magic numbers in the neutron excess nuclei is a representative example of the special features of the unstable nuclei. In this lecture of summer school, the problems of the magic number disappearance are presented. And the appearance of the deformation coexistence and the anomalous cluster structure come into the problem with them. At the begging the Antisymmetrized Molecular Dynamic (AMD) framework is explained with finite range two body central force and Gorgny DIS force composed of the zero range spin-orbit force and saturability. Island of inversion is explained in the nuclear chart shown in the figure and energy curves of the nuclei near 32 Mg and the excitation level schemes of 32 Mg are shown in the serial figures. As one of the extreme example of the nuclear structure the deformation of 19 F is picked up. The level schemes and structures of 21 F are shown as well. The molecule-like structure in the island of inversion is clear. The rotational band energy of fluorine isotopes are shown up to 29 F. As a new deformation area, disappearance of N=28 magic number is in the spotlight recently. In this case it is characteristic properties that the parities of the orbits to form the gap must be the same but the angular momenta should be different by 2. According to the AMD research, it is shown that deformations of prolate, three-axis asymmetric and oblate characters coexist in the very low excitation energy region accompanying the disappearance of N=28 gap. The concept of magic numbers has been very fundamental in nuclear physics since the success of shell model. At present its disappearance in the unstable nuclei is one of the most challenging problems in the understanding of the nuclear many body problems. (S. Funahashi)

Tunable fluorescence emission of ternary nonstoichiometric Ag-In-S alloyed nanocrystals

Energy Technology Data Exchange (ETDEWEB)

Feng Jian, E-mail: dhjfeng@ciac.jl.cn; Yang Xiurong, E-mail: xryang@ciac.jl.cn [Chinese Academy of Sciences, State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry (China)

2012-08-15

Low toxic, nonstoichiometric colloidal Ag-In-S ternary quantum dots with different Ag content were synthesized by a one-pot hot-injection method based on the reaction of metal acetylacetonates with sulfur dissolved in octadecene. X-ray diffraction (XRD), transmission electron microscopy, and high-resolution transmission electron microscopy (HRTEM) were used to characterize the size, structure, and morphology of these samples. ICP-MS was employed to analyze the compositions of Ag-In-S nanocrystals. The optical properties were characterized by UV-Vis absorption, photoluminescence (PL) spectroscopy, and time-resolved photoluminescence. Varying the fraction of cationic and capping agents, the compositions of Ag-In-S nanocrystals were precisely controlled. XRD and HRTEM results indicate the compositional homogeneity of Ag-In-S. The emission spectra across the different compositions exhibiting a single bandgap feature further confirm the formation of Ag-In-S alloy NCs, rather than phase separated Ag{sub 2}S and In{sub 2}S{sub 3}. Composition-dependent tunable PL emissions have been observed. The relative PL quantum yield is up to 16 %, which exhibited substantially enhanced comparing with the stoichiometric AgInS{sub 2} semiconductor core QDs reported in previous literature. The PL decay curve of Ag-In-S has a biexponential characteristic, which indicates that the recombination of an electron and a hole is dominated by the surface defect and the recombination process associated with internal traps is reduced significantly. The large Stokes shift between the absorption peaks and their emissions should inhibit the reabsorption and Foerster energy transfer between Ag-In-S nanocrystals, which provides the alternative in the further applications where high-concentrations of nanocrystals are needed.

Barrier bucket experiment at the AGS

Directory of Open Access Journals (Sweden)

M. Fujieda

1999-12-01

Full Text Available A barrier bucket experiment with two dedicated barrier cavities was performed at the Brookhaven AGS. One of the barrier cavities was a magnetic alloy (MA–loaded cavity and the other was a ferrite-loaded cavity. They generated a single sine wave with a peak voltage of 40 kV at a repetition rate of 351 kHz. A barrier rf system was established with these cavities and five bunches from the AGS booster were accumulated. A total of 3×10^{13} protons were stored without beam loss, and were successfully rebunched and accelerated. The longitudinal emittance growth was observed during accumulation by the barrier bucket, the blowup factor of which was about 3. The longitudinal mismatch between the rf bucket and the beam bunch was the main reason for the emittance growth. The potential distortions by beam loading of the ferrite cavity and the overshooting voltage of the MA cavity disturbed the smooth debunching.

Photocatalytic performance of graphene/TiO{sub 2}-Ag composites on amaranth dye degradation

Energy Technology Data Exchange (ETDEWEB)

Roşu, Marcela-Corina, E-mail: marcela.rosu@itim-cj.ro; Socaci, Crina; Floare-Avram, Veronica; Borodi, Gheorghe; Pogăcean, Florina; Coroş, Maria; Măgeruşan, Lidia; Pruneanu, Stela

2016-08-15

Ternary nanocomposites containing TiO{sub 2}, silver and graphene with different reduction levels were prepared and used as photocatalysts for amaranth azo dye degradation, under UV and natural light exposure. The obtained materials were characterized by TEM, XRD, FTIR and UV-Vis spectroscopy, confirming the successful formation of the nanocomposites. HPLC analysis along with UV-Vis spectroscopy were employed to quantify the concentration of non-degraded dye in solution. The graphene/TiO{sub 2}-Ag nanocomposites proved to have remarkable photocatalytic activities for amaranth degradation under UV and solar irradiation (85.3–98% of dye has disappeared in the first 2 h). Also, significant removal efficiencies (between 40.5 and 71.8%) of photocatalysts, in day light conditions, were demonstrated. The best result for amaranth dye degradation was obtained with the reduced graphene/TiO{sub 2}-Ag catalyst (up to 99.9%). Based on the degradation products analysis, a photodegradation pathway of amaranth dye was also proposed. - Highlights: • Graphene/TiO{sub 2}-Ag composites were prepared by a combined chemical-thermal method. • The composites showed improved light-absorption characteristics. • A significant degradation performance of amaranth was obtained with these composites under UV and natural light exposure. • Graphene/TiO{sub 2}-Ag composites offer a high potential for various photocatalytic applications in pollutant removal processes.

Visible light driven photocatalysis and antibacterial activity of AgVO{sub 3} and Ag/AgVO{sub 3} nanowires

Energy Technology Data Exchange (ETDEWEB)

Singh, Anamika [Department of Life Sciences, University of Mumbai, Santacruz (E), Mumbai 400 098 (India); Dutta, Dimple P., E-mail: dimpled@barc.gov.in [Chemistry Division, Bhabha Atomic Research Centre, Mumbai 400 085 (India); Ballal, A. [Molecular Biology Division, Bhabha Atomic Research Centre, Mumbai 400 085 (India); Tyagi, A.K. [Chemistry Division, Bhabha Atomic Research Centre, Mumbai 400 085 (India); Fulekar, M.H. [School of Environment and Sustainable Development, Central University of Gujarat, Gandhinagar 382 030, Gujarat (India)

2014-03-01

Graphical abstract: - Highlights: • Ag/AgVO{sub 3} and pure AgVO{sub 3} nanowires synthesized by sonochemical process. • Characterization done using XRD, SEM, TEM, EDX and BET analysis. • Visible light degradation of RhB by Ag/AgVO{sub 3} within 45 min. • Antibacterial activity of Ag/AgVO{sub 3} demonstrated. - Abstract: Ag/AgVO{sub 3} nanowires and AgVO{sub 3} nanorods were synthesized in aqueous media via a facile sonochemical route. The as-synthesized products were characterized by X-ray diffraction, Brunauer–Emmett–Teller surface area analysis, scanning electron microscopy together with an energy dispersion X-ray spectrum analysis, transmission electron microscopy and UV–vis diffuse reflectance spectroscopy. The results revealed that inert atmosphere promotes the formation of Ag/AgVO{sub 3} nanowires. The photocatalytic studies revealed that the Ag/AgVO{sub 3} nanowires exhibited complete photocatalytic degradation of Rhodamine B within 45 min under visible light irradiation. The antibacterial activity of Ag/AgVO{sub 3} nanowires was tested against Escherechia coli and Bacillus subtilis. The minimum growth inhibitory concentration value was found to be 50 and 10 folds lower than for the antibiotic ciprofloxacin for E. coli and B. subtilis, respectively. The antibacterial properties of the β-AgVO{sub 3} nanorods prove that in case of the Ag dispersed Ag/AgVO{sub 3} nanowires, the enhanced antibacterial action is also due to contribution from the AgVO{sub 3} support.

Experimental results on spin physics at the AGS

International Nuclear Information System (INIS)

Makdisi, Y.I.

1986-01-01

The AGS ran with polarized protons towards the end of 1985 and through the first two months of 1986. This comprised commissioning periods interleaved with two runs for physics at 13.5 GeV/c with beam polarization of 50 to 60%, and 18.5 GeV/c with an average beam polarization of 40%. Later, the AGS polarized beam reached peak energy of 22 GeV/c and polarization of 46%. This article describes the various spin related experimental efforts since the VI Symposium at Marseille. These will be grouped into those using unpolarized beams and the rest are the polarized proton beam users. Afterwards the future of the program is described as extensions of current experiments in addition to other measurements that are yet to be proposed

Thermochemical properties of silver tellurides including empressite (AgTe) and phase diagrams for Ag-Te and Ag-Te-O

Science.gov (United States)

Voronin, Mikhail V.; Osadchii, Evgeniy G.; Brichkina, Ekaterina A.

2017-10-01

This study compiles original experimental and literature data on the thermodynamic properties (ΔfG°, S°, ΔfH°) of silver tellurides (α-Ag2Te, β-Ag2Te, Ag1.9Te, Ag5Te3, AgTe) obtained by the method of solid-state galvanic cell with the RbAg4I5 and AgI solid electrolytes. The thermodynamic data for empressite (AgTe, pure fraction from Empress Josephine Mine, Colorado USA) have been obtained for the first time by the electrochemical experiment with the virtual reaction Ag + Te = AgTe. The Ag-Te phase diagrams in the T - x and log fTe2 (gas) - 1/ T coordinates have been refined, and the ternary Ag-Te-O diagrams with Ag-Te-TeO2 (paratellurite) composition range have been calculated.

One-pot synthesis of Ag-SiO2-Ag sandwich nanostructures

International Nuclear Information System (INIS)

Li Chaorong; Mei Jie; Li Shuwen; Lu Nianpeng; Wang Lina; Chen Benyong; Dong Wenjun

2010-01-01

Ag-SiO 2 -Ag sandwich nanostructures were prepared by a facile one-pot synthesis method. The Ag core, SiO 2 shell and Ag nanoparticle shell were all synthesized with polyvinylpyrrolidone, catalysed by ammonia, in the one-pot reaction. The polyvinylpyrrolidone, acting as a smart reducing agent, reduced the Ag + to Ag cores and Ag shells separately. Furthermore, the polyvinylpyrrolidone served as a protective agent to prevent the silver cores from aggregating. The SiO 2 shell and outer layer Ag nanoparticles were obtained when tetraethyl orthosilicate and ammonia were added to the silver core solution. Ammonia, acting as the catalyst, accelerated the hydrolysis of the tetraethyl orthosilicate to SiO 2 , which coated the silver cores. Furthermore, Ag(NH 3 ) 2 + ions were formed when aqueous ammonia was added to the solution, which increased the reduction capability. Then the polyvinylpyrrolidone reduced the Ag(NH 3 ) 2 + ions to small Ag nanoparticles on the surface of the Ag-SiO 2 and formed Ag-SiO 2 -Ag sandwich structures with a standard deviation of less than 4%. This structure effectively prevented the Ag nanoparticles on the silica surface from aggregating. Furthermore, the Ag-SiO 2 -Ag sandwich structures showed good catalysis properties due to the large surface area/volume value and activity of surface atoms of Ag particles.

Activated T lymphocytes disappear from circulation during endotoxemia in humans

DEFF Research Database (Denmark)

Suarez Krabbe, Karen; Kemp, Helle Bruunsgaard; Qvist, Jesper

2002-01-01

of disappearance were characterized by an activated phenotype (CD45RA(-) CD45RO(+)) as well as a phenotype linked to apoptosis (CD95(+) CD28(-)). In conclusion, endotoxin-induced lymphopenia reflects the disappearance from the circulation of activated lymphocytes prone to undergo apoptosis....

Fabrication of Ag/ZnO heterostructure and the role of surface coverage of ZnO microrods by Ag nanoparticles on the photophysical and photocatalytic properties of the metal-semiconductor system

Energy Technology Data Exchange (ETDEWEB)

Sarma, Bikash; Sarma, Bimal K., E-mail: sarmabimal@gmail.com

2017-07-15

Highlights: • Fabrication of Ag/ZnO heterostructure by facile chemical processes. • Decoration of plasmonic Ag nanoparticles on ZnO microrods through direct attachment. • Quenching of photoluminescence is observed in Ag/ZnO heterostructure. • Extent of surface coverage governs photophysical and photochemical properties. - Abstract: This report presents findings on microstructural, photophysical, and photocatalytic properties of Ag/ZnO heterostructure grown on flexible and silicon substrates. ZnO microrods are prepared by thermal decomposition method for different solute concentrations and Ag/ZnO heterostructure are fabricated by photo-deposition of Ag nanoparticles on ZnO microrods. X-ray diffraction and electron microscopy studies confirm that ZnO microrods belong to the hexagonal wurtzite structure and grown along [001] direction with random alignment showing that majority microrods are aligned with (100) face parallel to the sample surface. Plasmonic Ag nanoparticles are attached to different faces of ZnO. In the optical reflection spectra of Ag/ZnO heterostructure, the surface plasmon resonance peak due to Ag nanoparticles appears at 445 nm. Due to the oxygen vacancies the band gaps of ZnO microrods turn out to be narrower compared to that of bulk ZnO. The presence of Ag nanoparticles decreases the photoluminescence intensity which might be attributed to the non-radiative energy and direct electron transfer in the plasmon–exciton system. The quenching of photoluminescence in Ag/ZnO heterostructure at different growth conditions depend on the extent of surface coverage of ZnO by plasmonic Ag nanoparticles. Photocatalytic degradation efficiency of Ag/ZnO heterostructure is higher than that of ZnO microrods. The extent of surface coverage of ZnO microrods by Ag nanoparticles is crucial for the observed changes in photophysical and photochemical properties.

Flower-like Ag/AgCl microcrystals: Synthesis and photocatalytic activity

International Nuclear Information System (INIS)

Daupor, Hasan; Wongnawa, Sumpun

2015-01-01

Silver/silver chloride (Ag/AgCl) composites with a novel flower-like morphology were prepared via a hot precipitation assisted by the vinyl acetate monomer (VAM) route. An aqueous solution of AlCl 3 was mixed with the vinyl acetate monomer and acetic acid before adding a AgNO 3 solution at a temperature of 100 °C. The octapod shaped flower-like Ag/AgCl particles (or “flower-like Ag/AgCl” hereinafter) has eight petals each of which was about 7–11 μm in length. The flower-like octapods were formed by preferential overgrowth along the <111> directions of the cubic seeds. Detailed studies of the growth process at different AlCl 3 concentrations revealed that the concave cube developed into a Rubik's cube where eight corners grew further into the flower-like structures. The VAM and acetic acid concentration strongly affected the growth of the Ag/AgCl to the flower-like structure and their optimum concentrations were determined. The morphologies of these particles were carefully examined by scanning electron microscopy (SEM). The crystal structures and orientation relationship were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and UV–visible diffused reflectance spectroscopy (DRS). The flower-like Ag/AgCl microcrystals were tested for their photocatalytic degradation of orange G dye (OG) catalyzed by visible light. From comparative test runs, the flower-like Ag/AgCl exhibited better photocatalytic activity than simple and commercial Ag/AgCl particles. - Highlights: • Interesting transformation of microcrystals Ag/AgCl from concave cube via Rubik's cube to flower-like shape. • The first to use VAM as morphology control reagent. • High photocatalytic activity under visible light irradiation

VO(2peak), myocardial hypertrophy, and myocardial blood flow in endurance-trained men.

Science.gov (United States)

Laaksonen, Marko S; Heinonen, Ilkka; Luotolahti, Matti; Knuuti, Juhani; Kalliokoski, Kari K

2014-08-01

Endurance training induces cardiovascular and metabolic adaptations, leading to enhanced endurance capacity and exercise performance. Previous human studies have shown contradictory results in functional myocardial vascular adaptations to exercise training, and we hypothesized that this may be related to different degrees of hypertrophy in the trained heart. We studied the interrelationships between peak aerobic power (V˙O2peak), myocardial blood flow (MBF) at rest and during adenosine-induced vasodilation, and parameters of myocardial hypertrophy in endurance-trained (ET, n = 31) and untrained (n = 17) subjects. MBF and myocardial hypertrophy were studied using positron emission tomography and echocardiography, respectively. Both V˙O2peak (P negatively with adenosine-stimulated MBF, but when LV mass was taken into account as a partial correlate, this correlation disappeared. The present results show that increased LV mass in ET subjects explains the reduced hyperemic myocardial perfusion in this subject population and suggests that excessive LV hypertrophy has negative effect on cardiac blood flow capacity.

Ti-GO-Ag nanocomposite: the effect of content level on the antimicrobial activity and cytotoxicity.

Science.gov (United States)

Jin, Jianfeng; Zhang, Li; Shi, Mengqi; Zhang, Yumei; Wang, Qintao

2017-01-01

Surface modification of titanium (Ti) implants are extensively studied in order to obtain prominent biocompatibility and antimicrobial activity, especially preventing implant-associated infection. In this study, Ti substrates surface were modified by graphene oxide (GO) thin film and silver (Ag) nanoparticles via electroplating and ultraviolet reduction methods so as to achieve this purpose. Microstructures, distribution, quantities and spectral peaks of GO and Ag loading on the Ti sheets surface were characterized. GO-Ag-Ti multiphase nanocomposite exhibited excellent antimicrobial ability and anti-adherence performance. Subsequently, morphology, membrane integrity, apoptosis and relative genes expression of bacteria incubated on the Ti samples surface were monitored to reveal the bactericidal mechanism. Additionally, the cytotoxicity of Ti substrates incorporating GO thin film and Ag nanoparticles were investigated. GO-Ag-Ti composite configuration that have outstanding antibacterial properties will provide the foundation to study bone integration in vitro and in vivo in the future.

The effect of Ni pre-implantation on surface morphology and optical absorption properties of Ag nanoparticles embedded in SiO2

International Nuclear Information System (INIS)

Shen, Yanyan; Qi, Ting; Qiao, Yu; Yu, Shengwang; Hei, Hongjun; He, Zhiyong

2016-01-01

Graphical abstract: - Highlights: • Ag concentration increased significantly due to the Ni pre-implantation. • Deposition and accumulation process of Ag atoms depends on Ni fluences. • The incorporation of Ni elements in Ag NPs can damp SPR absorption intensity. • AgNi alloy NPs embedded in SiO 2 have been created by sequentially implantation. • Unique SPR absorption with dual peaks centered at 406 nm and 563 nm was observed. - Abstract: The effect of Ni ion fluence on Ag nucleation and particle growth was investigated by sequentially implantation of 60 keV Ni ions at fluences of 1 × 10 16 , 5 × 10 16 , 1 × 10 17 ions/cm 2 and 70 keV Ag ions at a fluence of 5 × 10 16 ions/cm 2 . Due to the modification of the deposition and accumulation process of Ag implants caused by Ni pre-implantation, the surface morphology, structures, and optical absorption properties of the Ag nanoparticles (NPs) depends strongly on the Ni fluences. UV–vis absorption spectroscopy study showed that the introducing of Ni atoms lead to intensity decrease in the Ag SPR band. Remarkable local concentration increase of Ag profiles appeared for the sample pre-implanted by Ni ions of 5.0 × 10 16 ions/cm 2 . In particular, the AgNi alloy NPs with dual absorption peaks centered at 406 nm and 563 nm have been formed after 600 °C annealing in Ar atmosphere. However, at a low fluence of 1.0 × 10 16 ions/cm 2 , only small increase of the local Ag concentration than the Ag ions singly implanted sample can be observed. At a high fluence of 1.0 × 10 17 ions/cm 2 , lots Ag atoms are trapped close to the surface, which result in heavy sputtering loss of Ag atoms and the sublimation of Ag atoms after 600 °C annealing.

Nano-Ag complexes prepared by γ-radiolysis and their structures and physical properties

International Nuclear Information System (INIS)

Kim, Hwa-Jung; Choi, Seong-Ho; Park, Hae-Jun

2012-01-01

In this study, nano-silver (nano-Ag) complexes showing different properties have been synthesized as follows. Polypyrrolidone (PVP)-stabilized silver colloids (NAg), nano-Ag bound to silica (SiO 2 ) (NSS), and nano-Ag bound to a complex of SiO 2 and polyaniline (PANI) (NSSPAI) were prepared via γ-irradiation at room temperature. NAg and NSS used PVP as a colloidal stabilizer, while NSSPAI did not use PVP as a colloidal stabilizer. Interesting bonding properties occurred in the nano-Ag complex and anticipated structural changes were clearly shown through a surface analysis of x-ray photoelectron spectroscopy (XPS). The morphologies by field emission-scanning electron microscopy (FE-SEM) analysis showed that nano-Ag complexes have various particle sizes ranging from 10 to 30 nm. NSS (average, 10 nm) and NSSPAI (average, 30 nm) showed a uniformly spherical shape and size, while NAg did not. From the reflection peaks in the x-ray diffraction (XRD) patterns, surface crystallinity of the nano-Ag complexes was indicated to be in the same degree as that of NSSPAI>NSS>NAg. Also, in the contact angle (CA) determination, surface hydrophobicity of NSSPAI was stronger than those of NSS and NAg, relatively. The different nano-Ag complexes prepared by γ-irradiation can be applicable in various industry fields due to the increase in specific property. - Highlights: ► Nano-Ag complexes showing different properties have been synthesized via γ-irradiation. ► Nano-Ag colloid (NAg), nano-Ag bound to SiO 2 (NSS), nano-Ag bound to SiO 2 and PANI complex (NSSPAI). ► Nano-Ag complexes were the same based on Ag metal. ► Results clearly showed fascinating/different physical properties. ► Different nano-Ag complexes can be applicable in various industry fields.

BROAD ABSORPTION LINE DISAPPEARANCE ON MULTI-YEAR TIMESCALES IN A LARGE QUASAR SAMPLE

Energy Technology Data Exchange (ETDEWEB)

Filiz Ak, N.; Brandt, W. N.; Schneider, D. P. [Department of Astronomy and Astrophysics, Pennsylvania State University, University Park, PA 16802 (United States); Hall, P. B. [Department of Physics and Astronomy, York University, 4700 Keele St., Toronto, Ontario M3J 1P3 (Canada); Anderson, S. F.; Gibson, R. R. [Astronomy Department, University of Washington, Seattle, WA 98195 (United States); Lundgren, B. F. [Department of Physics, Yale University, New Haven, CT 06511 (United States); Myers, A. D. [Department of Physics and Astronomy, University of Wyoming, Laramie, WY 82071 (United States); Petitjean, P. [Institut d' Astrophysique de Paris, Universite Paris 6, F-75014, Paris (France); Ross, Nicholas P. [Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, CA 92420 (United States); Shen Yue [Harvard-Smithsonian Center for Astrophysics, 60 Garden Street, MS-51, Cambridge, MA 02138 (United States); York, D. G. [Department of Astronomy and Astrophysics, and Enrico Fermi Institute, University of Chicago, 5640 S. Ellis Ave., Chicago, IL 60637 (United States); Bizyaev, D.; Brinkmann, J.; Malanushenko, E.; Oravetz, D. J.; Pan, K.; Simmons, A. E. [Apache Point Observatory, P.O. Box 59, Sunspot, NM 88349-0059 (United States); Weaver, B. A., E-mail: nfilizak@astro.psu.edu [Center for Cosmology and Particle Physics, New York University, New York, NY 10003 (United States)

2012-10-01

We present 21 examples of C IV broad absorption line (BAL) trough disappearance in 19 quasars selected from systematic multi-epoch observations of 582 bright BAL quasars (1.9 < z < 4.5) by the Sloan Digital Sky Survey-I/II (SDSS-I/II) and SDSS-III. The observations span 1.1-3.9 yr rest-frame timescales, longer than have been sampled in many previous BAL variability studies. On these timescales, Almost-Equal-To 2.3% of C IV BAL troughs disappear and Almost-Equal-To 3.3% of BAL quasars show a disappearing trough. These observed frequencies suggest that many C IV BAL absorbers spend on average at most a century along our line of sight to their quasar. Ten of the 19 BAL quasars showing C IV BAL disappearance have apparently transformed from BAL to non-BAL quasars; these are the first reported examples of such transformations. The BAL troughs that disappear tend to be those with small-to-moderate equivalent widths, relatively shallow depths, and high outflow velocities. Other non-disappearing C IV BALs in those nine objects having multiple troughs tend to weaken when one of them disappears, indicating a connection between the disappearing and non-disappearing troughs, even for velocity separations as large as 10,000-15,000 km s{sup -1}. We discuss possible origins of this connection including disk-wind rotation and changes in shielding gas.

Thermodynamic assessments of the Ag-Gd and Ag-Nd systems

International Nuclear Information System (INIS)

Wang, S.L.; Wang, C.P.; Liu, X.J.; Ishida, K.

2009-01-01

The phase diagrams and thermodynamic properties in the Ag-Re (Re: Gd, Nd) binary systems have been assessed by using the CALPHAD (Calculation of Phase Diagrams) method on the basis of the experimental data including the thermodynamic properties and phase equilibria. The Gibbs free energies of the liquid, bcc, fcc, dhcp and hcp phases were described by the subregular solution model with the Redlich-Kister equation, and those of the intermetallic compounds (Ag 51 Gd 14 , Ag 2 Gd, AgGd, Ag 51 Nd 14 , αAg 2 Nd, βAg 2 Nd and AgNd phases) in these two binary systems were described by the sublattice model. The thermodynamic parameters of each phase in the Ag-Re (Re: Gd, Nd) binary systems were obtained, and an agreement between the calculated results and experimental data was obtained in each binary system.

Curve thermoluminescent analysis of ZrO2 doped with nanoparticles and Ag nano fibers

International Nuclear Information System (INIS)

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

2008-01-01

This paper presents the results obtained from the analysis of the high temperature thermoluminescence response induced by UV radiation in pure zirconium (ZrO 2 ) and doped with Ag nanoparticles and Ag nano fibers. The zirconium samples were obtained by the sol-gel method and irradiated with a UV lamp for different times. The results showed that the presence of the dopants change the characteristics of the traps associated with the high temperature peak which is located at 230 C for pure zirconium, and that the greater influence is due the presence of Ag nano fibers, inducing a shift to lower temperatures. It also presents the thermoluminescence response as a function of irradiation time. (Author)

Stress disorders of families of the disappeared: a controlled study in Honduras.

Science.gov (United States)

Quirk, G J; Casco, L

1994-12-01

The effect of forced disappearance on the physical and psychological health of family members was assessed by interviews carried out in Honduras. Families of the disappeared were compared with two control groups: (1) families who lost a member due to accident or illness; and (2) families where no one had died within the past 10 years. Constellations of stress-related symptoms commonly seen in post-traumatic stress disorder and other anxiety disorders were approx. 2 times more prevalent in families of the disappeared as compared to the other two groups, indicating that families of the disappeared suffer over and above that due to normal grieving. It is suggested that the atmosphere of fear and isolation experienced by families of the disappeared is a causative factor in the prolongation of stress-related disorders years after the traumatic event.

Curve thermoluminescent analysis of ZrO{sub 2} doped with nanoparticles and Ag nano fibers; Analisis de la curva termoluminiscente de la ZrO{sub 2} dopada con nanoparticulas y nanofibras de Ag

Energy Technology Data Exchange (ETDEWEB)

Mendoza A, D.; Villa S, G.; Gutierrez W, C.; Perez H, R.; Gonzalez M, P. [ININ, Carretera Mexico-Toluca s/n, Ocoyoacac 52750, Estado de Mexico (Mexico)

2008-07-01

This paper presents the results obtained from the analysis of the high temperature thermoluminescence response induced by UV radiation in pure zirconium (ZrO{sub 2}) and doped with Ag nanoparticles and Ag nano fibers. The zirconium samples were obtained by the sol-gel method and irradiated with a UV lamp for different times. The results showed that the presence of the dopants change the characteristics of the traps associated with the high temperature peak which is located at 230 C for pure zirconium, and that the greater influence is due the presence of Ag nano fibers, inducing a shift to lower temperatures. It also presents the thermoluminescence response as a function of irradiation time. (Author)

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

Science.gov (United States)

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

2014-12-16

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

Optical properties of silver sulphide thin films formed on evaporated Ag by a simple sulphurization method

Energy Technology Data Exchange (ETDEWEB)

Barrera-Calva, E., E-mail: ebc@xanum.uam.m [Departamento de Ingenieria de Procesos e hidraulica, Universidad Autonoma Metropolitana - Iztapalapa, Av. Purisima Esq. Michoacan, Col. Vicentina, Mexico, D.F., 09340 (Mexico); Ortega-Lopez, M.; Avila-Garcia, A.; Matsumoto-Kwabara, Y. [Departamento de Ingenieria Electrica, Centro de Investigacion y de Estudios Avanzados del IPN, Mexico DF 07360 (Mexico)

2010-01-31

Silver sulphide (Ag{sub 2}S) thin films were grown on the surface of silver films (Ag) deposited on glass substrate by using a simple chemical sulphurization method. According to X-ray diffraction analysis, the Ag{sub 2}S thin films display low intensity peaks at 34.48{sup o}, 36.56{sup o}, and 44.28{sup o}, corresponding to diffraction from (100), (112) and (103) planes of the acanthite phase (monoclinic). A model of the type Ag{sub 2}S/Ag/glass was deduced from spectroscopic ellipsometric measurements. Also, the optical constants (n, k) of the system were determined. Furthermore, the optical properties as solar selective absorber for collector applications were assessed. The optical reflectance of the Ag{sub 2}S/Ag thin film systems exhibits the expected behavior for an ideal selective absorber, showing a low reflectance in the wavelength range below 2 {mu}m and a high reflectance for wavelengths higher than that value. An absorptance about 70% and an emittance about 3% or less were calculated for several samples.

The high-temperature modification of LuAgSn and high-pressure high-temperature experiments on DyAgSn, HoAgSn, and YbAgSn

Energy Technology Data Exchange (ETDEWEB)

Heying, B.; Rodewald, U.C.; Hermes, W.; Schappacher, F.M.; Riecken, J.F.; Poettgen, R. [Muenster Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie; Heymann, G.; Huppertz, H. [Muenchen Univ. (Germany). Dept. fuer Chemie und Biochemie; Sebastian, C.P. [Max-Planck-Institut fuer Chemische Physik Fester Stoffe, Dresden (Germany)

2008-02-15

The high-temperature modification of LuAgSn was obtained by arc-melting an equiatomic mixture of the elements followed by quenching the melt on a water-cooled copper crucible. HT-LuAgSn crystallizes with the NdPtSb-type structure, space group P6{sub 3}mc: a = 463.5(1), c = 723.2(1) pm, wR2 = 0.0270, 151 F{sup 2}, and 11 variables. The silver and tin atoms build up two-dimensional, puckered [Ag{sub 3}Sn{sub 3}] networks (276 pm Ag-Sn) that are charge-balanced and separated by the lutetium atoms. The Ag-Sn distances between the [Ag{sub 3}Sn{sub 3}] layers of 294 pm are much longer. Single crystals of isotypic DyAgSn (a = 468.3(1), c = 734.4(1) pm, wR2 = 0.0343, 411 F{sup 2}, and 11 variables) and HoAgSn (a = 467.2(1), c = 731.7(2) pm, wR2 = 0.0318, 330 F{sup 2}, and 11 variables) were obtained from arc-melted samples. Under high-pressure (up to 12.2 GPa) and high-temperature (up to 1470 K) conditions, no transitions to a ZrNiAl-related phase have been observed for DyAgSn, HoAgSn, and YbAgSn. HT-TmAgSn shows Curie-Weiss paramagnetism with {mu}{sub eff} = 7.53(1) {mu}{sub B}/Tm atom and {theta}P = -15.0(5) K. No magnetic ordering was evident down to 3 K. HT-LuAgSn is a Pauli paramagnet. Room-temperature {sup 119}Sn Moessbauer spectra of HT-TmAgSn and HT-LuAgSn show singlet resonances with isomer shifts of 1.78(1) and 1.72(1) mm/s, respectively. (orig.)

How do oocytes disappear?

Science.gov (United States)

Bonilla-Musoles, F; Renau, J; Hernandez-Yago, J; Torres, J

1975-07-29

It has been study using transmission and scanner electron microscopy the mean procedures of dessaparence of the oocytes. On described three methods: 1. The necrosis of the oocytes. 2. The autolysis and fagocitosis by granulosa cells. 3. The migration of those to the superphicie and fall into the peritoneal cavity. Using the scanner electron microscopy in ovaries of fetus and newborn it seems the latest method to bee the most important during the intrauterine life. After the birth, this last phenomenon seems to disappear.

In situ solid-state fabrication of hybrid AgCl/AgI/AgIO3 with improved UV-to-visible photocatalytic performance.

Science.gov (United States)

Xie, Jing; Cao, Yali; Jia, Dianzeng; Li, Yizhao; Wang, Kun; Xu, Hui

2017-09-28

The AgCl/AgI/AgIO 3 composites were synthesized through a one-pot room-temperature in situ solid-state approach with the feature of convenient and eco-friendly. The as-prepared composites exhibit superior photocatalytic performance than pure AgIO 3 for the degradation of methyl orange (MO) under both UV and visible light irradiation. The photodegradation rate toward MO of the AgCl/AgI/AgIO 3 photocatalyst can reach 100% after 12 min irradiation under UV light, or 85.4% after 50 min irradiation under visible light, being significantly higher than AgCl, AgI, AgIO 3 and AgI/AgIO 3 . In addition, the AgCl/AgI/AgIO 3 photocatalyst possesses strong photooxidation ability for the degradation of rhodamine B (RhB), methylene blue (MB), phenol, bisphenol A (BPA) and tetracycline hydrochloride under visible light irradiation. The reactive species capture experiments confirmed that the h + and •O 2- play an essential role during the photocatalytic process under UV light or visible light irradiation. The enhanced effect may be beneficial from the enhanced light adsorption in full spectrum and increased separation efficiency of photogenerated hole-electron pairs, which can be ascribed to the synergistic effect among AgCl, AgI and AgIO 3 nanoplates in AgCl/AgI/AgIO 3 composites.

PANI-Ag-Cu Nanocomposite Thin Films Based Impedimetric Microbial Sensor for Detection of E. coli Bacteria

Directory of Open Access Journals (Sweden)

Huda Abdullah

2014-01-01

Full Text Available PANI-Ag-Cu nanocomposite thin films were prepared by sol-gel method and deposited on the glass substrate using spin coating technique. Polyaniline was synthesized by chemical oxidative polymerization of aniline monomer in the presence of nitric acid. The films were characterized using XRD, FTIR, and UV-Visible spectroscopy. The performance of the sensor was conducted using electrochemical impedance spectroscopy to obtain the change in impedance of the sensor film before and after incubation with E. coli bacteria in water. The peaks in XRD pattern confirm the presence of Ag and Cu nanoparticles in face-centered cubic structure. FTIR analysis shows the stretching of N–H in the polyaniline structure. The absorption band from UV-Visible spectroscopy shows high peaks between 400 nm and 500 nm which indicate the presence of Ag and Cu nanoparticles, respectively. Impedance analysis indicates that the change in impedance of the films decreases with the presence of E. coli. The sensitivity on E. coli increases for the sample with high concentration of Cu.

Search for sterile neutrinos in muon neutrino disappearance mode at FNAL

International Nuclear Information System (INIS)

Anokhina, A.; Dzhatdoev, T.; Morgunova, O.; Roganova, T.; Bagulya, A.; Chernyavskiy, M.; Dalkarov, O.; Mingazheva, R.; Shchedrina, T.; Starkov, N.; Vladymyrov, M.; Benettoni, M.; Dal Corso, F.; Dusini, S.; Lippi, I.; Longhin, A.; Bernardini, P.; Mancarella, G.; Marsella, G.; Brugnera, R.; Garfagnini, A.; Medinaceli, E.; Roda, M.; Sirignano, C.; Calabrese, M.; Fiore, G.; Surdo, A.; Cecchetti, A.; Orecchini, D.; Paoloni, A.; Cecchini, S.; Di Ferdinando, D.; Guerzoni, M.; Laurenti, G.; Mandrioli, G.; Mauri, N.; Patrizii, L.; Pozzato, M.; Sahnoun, Z.; Sirri, G.; Togo, V.; Del Prete, A.; Papadia, G.; De Robertis, G.; Fini, R.A.; Loddo, F.; Pastore, A.; De Serio, M.; Paparella, L.; Simone, S.; Klicek, B.; Jakovcic, K.; Malenica, M.; Stipcevic, M.; Kose, U.; Nessi, M.; Margiotta, A.; Pasqualini, L.; Spurio, M.; Muciaccia, M.T.; Polukhina, N.; Rosa, G.; Stanco, L.; Tenti, M.

2017-01-01

The NESSiE Collaboration has been setup to undertake a conclusive experiment to clarify the muon-neutrino disappearance measurements at short baselines in order to put severe constraints to models with more than the three-standard neutrinos. To this aim the current FNAL-Booster neutrino beam for a Short-Baseline experiment was carefully evaluated by considering the use of magnetic spectrometers at two sites, near and far ones. The detector locations were studied, together with the achievable performances of two OPERA-like spectrometers. The study was constrained by the availability of existing hardware and a time-schedule compatible with the undergoing project of multi-site Liquid-Argon detectors at FNAL. The settled physics case and the kind of proposed experiment on the Booster neutrino beam would definitively clarify the existing tension between the ν μ disappearance and the ν e appearance/disappearance at the eV mass scale. In the context of neutrino oscillations the measurement of ν μ disappearance is a robust and fast approach to either reject or discover new neutrino states at the eV mass scale. We discuss an experimental program able to extend by more than one order of magnitude (for neutrino disappearance) and by almost one order of magnitude (for antineutrino disappearance) the present range of sensitivity for the mixing angle between standard and sterile neutrinos. These extensions are larger than those achieved in any other proposal presented so far. (orig.)

Search for sterile neutrinos in muon neutrino disappearance mode at FNAL

Science.gov (United States)

Anokhina, A.; Bagulya, A.; Benettoni, M.; Bernardini, P.; Brugnera, R.; Calabrese, M.; Cecchetti, A.; Cecchini, S.; Chernyavskiy, M.; Dal Corso, F.; Dalkarov, O.; Del Prete, A.; De Robertis, G.; De Serio, M.; Di Ferdinando, D.; Dusini, S.; Dzhatdoev, T.; Fini, R. A.; Fiore, G.; Garfagnini, A.; Guerzoni, M.; Klicek, B.; Kose, U.; Jakovcic, K.; Laurenti, G.; Lippi, I.; Loddo, F.; Longhin, A.; Malenica, M.; Mancarella, G.; Mandrioli, G.; Margiotta, A.; Marsella, G.; Mauri, N.; Medinaceli, E.; Mingazheva, R.; Morgunova, O.; Muciaccia, M. T.; Nessi, M.; Orecchini, D.; Paoloni, A.; Papadia, G.; Paparella, L.; Pasqualini, L.; Pastore, A.; Patrizii, L.; Polukhina, N.; Pozzato, M.; Roda, M.; Roganova, T.; Rosa, G.; Sahnoun, Z.; Shchedrina, T.; Simone, S.; Sirignano, C.; Sirri, G.; Spurio, M.; Stanco, L.; Starkov, N.; Stipcevic, M.; Surdo, A.; Tenti, M.; Togo, V.; Vladymyrov, M.

2017-01-01

The NESSiE Collaboration has been setup to undertake a conclusive experiment to clarify the muon-neutrino disappearance measurements at short baselines in order to put severe constraints to models with more than the three-standard neutrinos. To this aim the current FNAL-Booster neutrino beam for a Short-Baseline experiment was carefully evaluated by considering the use of magnetic spectrometers at two sites, near and far ones. The detector locations were studied, together with the achievable performances of two OPERA-like spectrometers. The study was constrained by the availability of existing hardware and a time-schedule compatible with the undergoing project of multi-site Liquid-Argon detectors at FNAL. The settled physics case and the kind of proposed experiment on the Booster neutrino beam would definitively clarify the existing tension between the ν _{μ } disappearance and the ν e appearance/disappearance at the eV mass scale. In the context of neutrino oscillations the measurement of ν _{μ } disappearance is a robust and fast approach to either reject or discover new neutrino states at the eV mass scale. We discuss an experimental program able to extend by more than one order of magnitude (for neutrino disappearance) and by almost one order of magnitude (for antineutrino disappearance) the present range of sensitivity for the mixing angle between standard and sterile neutrinos. These extensions are larger than those achieved in any other proposal presented so far.

Search for sterile neutrinos in muon neutrino disappearance mode at FNAL

Energy Technology Data Exchange (ETDEWEB)

Anokhina, A.; Dzhatdoev, T.; Morgunova, O.; Roganova, T. [Lomonosov Moscow State University (MSU SINP), Moscow (Russian Federation); Bagulya, A.; Chernyavskiy, M.; Dalkarov, O.; Mingazheva, R.; Shchedrina, T.; Starkov, N.; Vladymyrov, M. [Lebedev Physical Institute of Russian Academy of Sciences, Moscow (Russian Federation); Benettoni, M.; Dal Corso, F.; Dusini, S.; Lippi, I.; Longhin, A. [INFN, Sezione di Padova, Padua (Italy); Bernardini, P.; Mancarella, G.; Marsella, G. [Universita del Salento, Dipartimento di Matematica e Fisica, Lecce (Italy); INFN, Sezione di Lecce, Lecce (Italy); Brugnera, R.; Garfagnini, A.; Medinaceli, E.; Roda, M.; Sirignano, C. [INFN, Sezione di Padova, Padua (Italy); Universita di Padova, Dipartimento di Fisica e Astronomia, Padua (Italy); Calabrese, M.; Fiore, G.; Surdo, A. [INFN, Sezione di Lecce, Lecce (Italy); Cecchetti, A.; Orecchini, D.; Paoloni, A. [INFN, Laboratori Nazionali di Frascati, Frascati, RM (Italy); Cecchini, S.; Di Ferdinando, D.; Guerzoni, M.; Laurenti, G.; Mandrioli, G.; Mauri, N.; Patrizii, L.; Pozzato, M.; Sahnoun, Z.; Sirri, G.; Togo, V. [INFN, Sezione di Bologna, Bologna (Italy); Del Prete, A.; Papadia, G. [INFN, Sezione di Lecce, Lecce (Italy); Universita del Salento, Dipartimento di Ingegneria dell' Innovazione, Lecce (Italy); De Robertis, G.; Fini, R.A.; Loddo, F.; Pastore, A. [INFN, Sezione di Bari, Bari (Italy); De Serio, M.; Paparella, L.; Simone, S. [INFN, Sezione di Bari, Bari (Italy); Universita di Bari, Dipartimento di Fisica, Bari (Italy); Klicek, B.; Jakovcic, K.; Malenica, M.; Stipcevic, M. [Rudjer Boskovic Institute, Zagreb (Croatia); Kose, U.; Nessi, M. [European Organization for Nuclear Research (CERN), Geneva (Switzerland); Margiotta, A.; Pasqualini, L.; Spurio, M. [INFN, Sezione di Bologna, Bologna (Italy); Universita di Bologna, Dipartimento di Fisica e Astronomia, Bologna (Italy); Muciaccia, M.T. [Universita di Bari, Dipartimento di Fisica, Bari (Italy); Polukhina, N. [Lebedev Physical Institute of Russian Academy of Sciences, Moscow (Russian Federation); National Research Nuclear University MEPhI, Moscow (Russian Federation); Rosa, G. [INFN, Sezione di Roma, Rome (Italy); Stanco, L. [INFN, Sezione di Padova, Padua (Italy); Tenti, M. [Universita di Bologna, Dipartimento di Fisica e Astronomia, Bologna (Italy); NFN-CNAF, Bologna (Italy)

2017-01-15

The NESSiE Collaboration has been setup to undertake a conclusive experiment to clarify the muon-neutrino disappearance measurements at short baselines in order to put severe constraints to models with more than the three-standard neutrinos. To this aim the current FNAL-Booster neutrino beam for a Short-Baseline experiment was carefully evaluated by considering the use of magnetic spectrometers at two sites, near and far ones. The detector locations were studied, together with the achievable performances of two OPERA-like spectrometers. The study was constrained by the availability of existing hardware and a time-schedule compatible with the undergoing project of multi-site Liquid-Argon detectors at FNAL. The settled physics case and the kind of proposed experiment on the Booster neutrino beam would definitively clarify the existing tension between the ν{sub μ} disappearance and the ν{sub e} appearance/disappearance at the eV mass scale. In the context of neutrino oscillations the measurement of ν{sub μ} disappearance is a robust and fast approach to either reject or discover new neutrino states at the eV mass scale. We discuss an experimental program able to extend by more than one order of magnitude (for neutrino disappearance) and by almost one order of magnitude (for antineutrino disappearance) the present range of sensitivity for the mixing angle between standard and sterile neutrinos. These extensions are larger than those achieved in any other proposal presented so far. (orig.)

Development of a 3D muon disappearance algorithm for muon scattering tomography

Science.gov (United States)

Blackwell, T. B.; Kudryavtsev, V. A.

2015-05-01

Upon passing through a material, muons lose energy, scatter off nuclei and atomic electrons, and can stop in the material. Muons will more readily lose energy in higher density materials. Therefore multiple muon disappearances within a localized volume may signal the presence of high-density materials. We have developed a new technique that improves the sensitivity of standard muon scattering tomography. This technique exploits these muon disappearances to perform non-destructive assay of an inspected volume. Muons that disappear have their track evaluated using a 3D line extrapolation algorithm, which is in turn used to construct a 3D tomographic image of the inspected volume. Results of Monte Carlo simulations that measure muon disappearance in different types of target materials are presented. The ability to differentiate between different density materials using the 3D line extrapolation algorithm is established. Finally the capability of this new muon disappearance technique to enhance muon scattering tomography techniques in detecting shielded HEU in cargo containers has been demonstrated.

SIMULATIONS OF THE AGS MMPS STORING ENERGY IN CAPACITOR BANKS

International Nuclear Information System (INIS)

MARNERIS, I.; BADEA, V.S.; BONATI, R.; ROSER, T.; SANDBERG, J.

2007-01-01

The Brookhaven AGS Main Magnet Power Supply (MMPS) is a thyristor control supply rated at 5500 Amps, +/-9000 Volts. The peak magnet power is 50 MWatts. The power supply is fed from a motor/generator manufactured by Siemens. The generator is 3 phase 7500 Volts rated at 50 MVA. The peak power requirements come from the stored energy in the rotor of the motor/generator. The motor generator is about 45 years old, made by Siemens and it is not clear if companies will be manufacturing similar machines in the future. We are therefore investigating different ways of storing energy for future AGS MMPS operations. This paper will present simulations of a power supply where energy is stored in capacitor banks. Two dc to dc converters will be presented along with the control system of the power section. The switching elements will be IGCT's made by ABB. The simulation program used is called PSIM version 6.1. The average power from the local power authority into the power supply will be kept constant during the pulsing of the magnets at +/-50 MW. The reactive power will also be kept constant below 1.5 MVAR. Waveforms will be presented

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.

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.

Effect of different treatments on 110m Ag plant uptake in various soil types

International Nuclear Information System (INIS)

Szerbin, P.; Koblinger-Bokori, E.

1996-01-01

110m Ag contamination may occur as a result of atmospheric release either during normal operation of nuclear power plants or in accidental circumstances. The gamma peaks of 110m Ag and radiocaesium are very close, and not every laboratory could make distinction between them. Therefore very few references are available on 110m Ag environmental behaviour and plant uptake. In the present study plant uptake of 110m Ag from four different types of soil was investigated, and the results are presented in relation to major soil characteristics. In addition, effects of two different treatments (phosphate and organic matter fertilizations) are determined in each type of soil. Our study clearly demonstrates that a carefully selected post-accident treatment can significantly reduce the environmental consequences of radioactive releases. Methods to be developed on bases of such studies could be used for remedial actions of agricultural lands polluted with radioactive substances

Nonlinear-Optical and Fluorescent Properties of Ag Aqueous Colloid Prepared by Silver Nitrate Reduction

Directory of Open Access Journals (Sweden)

Xiaoqiang Zhang

2010-01-01

Full Text Available The nonlinear-optical properties of metal Ag colloidal solutions, which were prepared by the reduction of silver nitrate, were investigated using Z-scan method. Under picosecond 532 nm excitation, the Ag colloidal solution exhibited negative nonlinear refractive index (n2=−5.17×10−4 cm2/W and reverse saturable absorption coefficient (β=4.32 cm/GW. The data fitting result of optical limiting (OL response of metal Ag colloidal solution indicated that the nonlinear absorption was attributed to two-photon absorption effect at 532 nm. Moreover, the fluorescence emission spectra of Ag colloidal solution were recorded under excitations at both 280 nm and 350 nm. Two fluorescence peaks, 336 nm and 543 nm for 280 nm excitation, while 544 nm and 694 nm for 350 nm excitation, were observed.

Tem Observation Of Precipitate Structures In Al-Zn-Mg Alloys With Additions Of Cu/Ag

Directory of Open Access Journals (Sweden)

Watanabe K.

2015-06-01

Full Text Available Al-Zn-Mg alloy has been known as one of the aluminum alloys with the good age-hardening ability and the high strength among commercial aluminum alloys. The mechanical property of the limited ductility, however, is required to further improvement. In this work, three alloys, which were added Cu or Ag into the Al-Zn-Mg alloy, were prepared to compare the effect of the additional elements on the aging behavior. The content of Ag and Cu were 0.2at.% and the same as, respectively. Ag or Cu added alloy showed higher maximum hardness than base alloy. The particle shape and rod shape precipitates were observed in all alloys peak-aged at 423K. According to addition of Ag or Cu, the number density of the precipitates increased higher than that of base alloy.

Microstructure and mechanical properties of Al-Cu-Mg-Mn-Zr alloy with trace amounts of Ag

International Nuclear Information System (INIS)

Liu Xiaoyan; Pan Qinglin; Lu Congge; He Yunbin; Li Wenbin; Liang Wenjie

2009-01-01

The microstructure and mechanical properties of Al-Cu-Mg-(Ag)-Mn-Zr alloys were studied by means of tensile testing, optical microscopy (OM), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The results show that small additions of Ag to Al-Cu-Mg-Mn-Zr alloy can accelerate the hardening effect of the aged alloy and reduce the time to peak-aged. The mechanical properties can be improved both at room temperature and at elevated temperatures, which is attributed to the fine and uniform plate-like Ω precipitates. Meanwhile the ductility of the studied alloys remains at relatively high level. The major strengthening phases of the Ag-free alloy are θ' and less S', while that of Al-Cu-Mg-Mn-Zr alloy containing trace amounts of Ag are Ω and less θ'.

Occurrence, characterisation and fate of (nano)particulate Ti and Ag in two Norwegian wastewater treatment plant

DEFF Research Database (Denmark)

Polesel, Fabio; Farkas, Julia; Kjos, Marianne

2018-01-01

was conducted in two full-scale WWTPs in Trondheim (Norway) employing only primary treatment. We assessed the occurrence and elimination of Ti and Ag, and conducted size-based fractionation using sequential filtration of influent samples to separate particulate, colloidal and dissolved fractions. Eight......-hour composite influent samples were collected to assess diurnal variations in total Ti and Ag influx. Measured influent Ti concentrations (up to 290 μg L−1) were significantly higher than Ag (solids (>0.7 μm). Removal efficiencies ≥70% were observed....... Diurnal profiles of influent Ti were correlated to flow and pollutant concentration patterns (especially total suspended solids), with peaks during the morning and/or evening and minima at night, indicating household discharges as predominant source. Irregular profiles were exhibited by influent Ag...

Facile synthesis, structure, and properties of Ag{sub 2}S/Ag heteronanostructure

Energy Technology Data Exchange (ETDEWEB)

Sadovnikov, S. I., E-mail: sadovnikov@ihim.uran.ru; Gusev, A. I. [Ural Branch of the Russian Academy of Sciences, Institute of Solid State Chemistry (Russian Federation)

2016-09-15

Ag{sub 2}S/Ag heteronanostructure has been produced by a simple one-stage chemical deposition from aqueous solutions of silver nitrate, sodium sulfide, and sodium citrate with the use of monochromatic light irradiation. For simultaneous synthesis of Ag{sub 2}S and Ag nanoparticles, deposition has been performed from reaction mixtures with reduced sodium sulfide concentration. The size of Ag{sub 2}S and Ag nanoparticles is 45–50 and 15–20 nm, respectively. It is established that in the contact layer between silver sulfide and silver, nonconducting α-Ag{sub 2}S acanthite transforms into superionic β-Ag{sub 2}S argentite under the action of external electric field. The scheme of the operation of a resistive switch based on an Ag{sub 2}S/Ag heteronanostructure is proposed. The UV–Vis optical absorption spectra of colloidal solutions of Ag{sub 2}S/Ag heteronanostructures have been studied.Graphical Abstract.

Antibacterial Ag/a-C nanocomposite coatings: The influence of nano-galvanic a-C and Ag couples on Ag ionization rates

Energy Technology Data Exchange (ETDEWEB)

Manninen, N.K., E-mail: nora.sousa@dem.uc.pt [SEG-CEMUC, Mechanical Engineering Department, University of Coimbra, 3030-788 Coimbra (Portugal); GRF-CFUM, Physics Department, University of Minho, Campus of Azurém, 4800-058 Guimarães (Portugal); Calderon, S. [SEG-CEMUC, Mechanical Engineering Department, University of Coimbra, 3030-788 Coimbra (Portugal); GRF-CFUM, Physics Department, University of Minho, Campus of Azurém, 4800-058 Guimarães (Portugal); Carvalho, I. [GRF-CFUM, Physics Department, University of Minho, Campus of Azurém, 4800-058 Guimarães (Portugal); CEB—Centre of Biological Engineering, LIBRO-Laboratório de Investigação em Biofilmes Rosário Oliveira, University of Minho, 4710-057 Braga (Portugal); Henriques, M. [CEB—Centre of Biological Engineering, LIBRO-Laboratório de Investigação em Biofilmes Rosário Oliveira, University of Minho, 4710-057 Braga (Portugal); Cavaleiro, A. [SEG-CEMUC, Mechanical Engineering Department, University of Coimbra, 3030-788 Coimbra (Portugal); Carvalho, S. [SEG-CEMUC, Mechanical Engineering Department, University of Coimbra, 3030-788 Coimbra (Portugal); GRF-CFUM, Physics Department, University of Minho, Campus of Azurém, 4800-058 Guimarães (Portugal)

2016-07-30

Highlights: • Amorphous carbon (a-C), Ag/a-C and Ag coatings were deposited by magnetron sputtering. • a-C/Ag coating shows antibacterial activity against S. epidermidis. • The formation of nano-galvanic couples in a-C/Ag enhances the Ag{sup +} ionization rate. • The Ag{sup +} ionization occurs along with Ag nanoparticles agglomeration in 0.9% NaCl. - Abstract: Biofilm formation has been pointed as a major concern in different industrial applications, namely on biomedical implants and surgical instruments, which has prompted the development of new strategies for production of efficient antimicrobial surfaces. In this work, nano-galvanic couples were created to enhance the antibacterial properties of silver, by embedding it into amorphous carbon (a-C) matrix. The developed Ag/a-C nanocomposite coatings, deposited by magnetron sputtering, revealed an outstanding antibacterial activity against Staphylococcus epidermidis, promoting a total reduction in biofilm formation with no bacteria counts in all dilution. The open circuit potential (OCP) tests in 0.9% NaCl confirmed that a-C shows a positive OCP value, in contrast to Ag coating, thus enhancing the ionization of biocidal Ag{sup +} due to the nano-galvanic couple activation. This result was confirmed by the inductively coupled plasma-optical emission spectroscopy (ICP-OES), which revealed a higher Ag ionization rate in the nanocomposite coating in comparison with the Ag coating. The surface of Ag/a-C and Ag coatings immersed in 0.9% NaCl were monitored by scanning electron microscopy (SEM) over a period of 24 h, being found that the Ag ionization determined by ICP-OES was accompanied by an Ag nanoparticles coalescence and agglomeration in Ag/a-C coating.

The negative temperature coefficient resistivities of Ag2S-Ag core–shell structures

International Nuclear Information System (INIS)

Yu, Mingming; Liu, Dongzhi; Li, Wei; Zhou, Xueqin

2014-01-01

In this paper, the conductivity of silver nanoparticle films protected by 3-mercaptopropionic acid (Ag/MPA) has been investigated. When the nanoparticles were annealed in air at 200 °C, they converted to stable Ag 2 S-Ag core–shell structures. The mechanism for the formation of the Ag 2 S-Ag core–shell structures along with the compositional changes and the microstructural evolution of the Ag/MPA nanoparticles during the annealing process are discussed. It is proposed that the Ag 2 S-Ag core–shell structure was formed through a solid-state reduction reaction, in which the Ag + ions coming from Ag 2 S were reduced by sulfonate species and sulfur ions. The final Ag 2 S-Ag films display an exponentially decreased resistivity with increasing temperature from 25 to 170 °C. The negative temperature coefficient resistivity of Ag 2 S-Ag films can be adjusted by changing the S/Ag molar ratio used for the synthesis of the Ag/MPA nanoparticles, paving the way for the preparation of negative temperature-coefficient thermistors via printing technology for use in the electronics.

Disappearance of a detached vapor mass in subcooled water

International Nuclear Information System (INIS)

Inada, Shigeaki; Miyasaka, Yoshiki; Izumi, Ryotaro.

1986-01-01

Experiments on pool transition boiling of water under atmospheric pressure on a heated surface 10 mm in diameter were conducted for subcooling 15 - 50 K. The mass flux of condensation of a detached coalescent vapor bubble was experimentally estimated by a mathematical model based on the mass transfer mechanism of condensation. As a result, it is clarified that the mass flux of condensation of the detached bubble was influenced by the initial growing velocity of a vapor bubble immediately following the detached bubble. The disappearance velocity of the detached bubble defined as a ratio of the bubble diameter at the departure to the time required until the disappearance, is in the range 0.2 to 2.0 m/sec. The disappearance velocity is proportional to the initial growing velocity of the bubble, to the square of the heat flux of the heated surface and to the cube of the wall superheat, separately. (author)

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.

Chronic oral lactate supplementation does not affect lactate disappearance from blood after exercise

DEFF Research Database (Denmark)

Brouns, F; Fogelholm, M; Van Hall, Gerrit

1995-01-01

This study tested the hypothesis that a 3-week oral lactate supplementation affects postexercise blood lactate disappearance in untrained male subjects. Fifteen men were randomly assigned to either a lactate supplementation (n = 8) or a placebo (n = 7) treatment. During the treatment period...... they drank an oral lactate or a maltodextrin (placebo) supplement twice a day. The lactate drink contained 10 g of lactate as calcium, sodium, and potassium salts. Blood lactate concentrations were studied before, during, and immediately after three exercise tests, both pre- and posttreatment. Peak lactate...... values for placebo (PL) or lactate (L) treatment groups during different tests were as follows: Test 1 PL, 13.49 +/- 3.71; L, 13.70 +/- 1.90; Test 2 PL, 12.64 +/- 2.32; L, 12.00 +/- 2.23; Test 3 PL, 12.29 +/- 2.92; L, 11.35 +/- 1.38 and were reached 3 min postexercise. The decrease in blood lactate...

Analysis of the residual strain change of Bi2212, Ag alloy and Ag during the heating and cooling process in Bi2212/Ag/Ag alloy composite wire

International Nuclear Information System (INIS)

Shin, J K; Ochiai, S; Okuda, H; Mukai, Y; Sugano, M; Sato, M; Oh, S S; Ha, D W; Kim, S C

2008-01-01

The residual strain change of Bi2212 and Ag during the cooling and heating process in the Bi2212/Ag/Ag alloy composite superconductor was studied. First, the residual strain of Bi2212 filaments at room temperature was measured by the x-ray diffraction method. Then, the Young's moduli of the constituents (Bi2212 filaments, Ag and Ag alloy) and yield strains of Ag and Ag alloy were estimated from the analysis of the measured stress-strain curve, based on the rule of mixtures. Also, the coefficient of thermal expansion of the Bi2212 filaments was estimated from the analysis of the measured thermal expansion curve of the composite wire. From the modeling analysis using the estimated property values and the residual strain of Bi2212 filaments, the changes of residual strain of Bi2212, Ag alloy and Ag with temperature during the cooling and heating process were revealed

Forced disappearance in an era of globalization: biopolitics, shadow networks, and imagined worlds.

Science.gov (United States)

Rozema, Ralph

2011-01-01

In this article, I argue that the practice of forced disappearance of persons on the part of paramilitary groups has become linked to specific processes of globalization. Global flows related to biopolitics, global crime networks, and dehumanizing imaginations reproduced by mass media together constitute a driving force behind forced disappearances. Drawing on ethnographic fieldwork in the Colombian city of Medellín, I analyze how these global flows interact with local armed actors, helping create a climate conducive to forced disappearance. These mechanisms in Colombia show similarities to those in some African and Asian countries. Gaining insight into the mechanisms behind forced disappearance may help prevent it from occurring in the future. Enhancing social inclusion of residents, unraveling the transnational crime networks in which perpetrators are involved, and disseminating rehumanizing images of victims all contribute to curbing the practice of forced disappearance.

Structure analysis of complex metallic alloys in the Eu-Ag-In system by X-ray diffraction

International Nuclear Information System (INIS)

Gomez, Cesar Pay; Morita, Yoshiki; Tsai, An Pang; Yamamoto, Akiji

2009-01-01

In this work we investigate the complex atomic structures of two CMAs in the Eu-Ag-In system, these are quasicrystal approximants and their structures are similar to those of the 1/1 and 2/1 approximants found in the Yb-Cd system. The similarities between the Yb-Cd and Eu-Ag-In systems indicate that the RE-Ag-In systems in several ways can be treated as pseudo-binary. The investigated phases however also show some interesting differences; when Cd is replaced by the elements Ag and In partial chemical disorder is introduced into the system. As a response, the positional disorder which is usually observed in certain atomic positions for these types of approximants tends to disappear. The complete structures refined from single crystal data are described in detail and the differences with other related phases are highlighted. The 2/1 approximant in the Eu-Ag-In system is the first to exhibit such a degree of structural perfection in terms of positional order, a feature which makes this phase very suitable for further studies of chemical order and also can give insight into the local structures of related disordered phases. Electron diffraction studies on the 1/1 approximant phase have previously shown the presence of weak superlattice reflections, indicating a superstructure similar to that of the related phase Eu 4 Cd 25 . However, no superlattice reflections could be observed by single crystal diffraction and it is thus concluded that the phase has a disordered average structure with possible short to medium range superlattice ordering.

Comparative Study of Antimicrobial Activity of AgBr and Ag Nanoparticles (NPs)

Science.gov (United States)

Suchomel, Petr; Kvitek, Libor; Panacek, Ales; Prucek, Robert; Hrbac, Jan; Vecerova, Renata; Zboril, Radek

2015-01-01

The diverse mechanism of antimicrobial activity of Ag and AgBr nanoparticles against gram-positive and gram-negative bacteria and also against several strains of candida was explored in this study. The AgBr nanoparticles (NPs) were prepared by simple precipitation of silver nitrate by potassium bromide in the presence of stabilizing polymers. The used polymers (PEG, PVP, PVA, and HEC) influence significantly the size of the prepared AgBr NPs dependently on the mode of interaction of polymer with Ag+ ions. Small NPs (diameter of about 60–70 nm) were formed in the presence of the polymer with low interaction as are PEG and HEC, the polymers which interact with Ag+ strongly produce nearly two times bigger NPs (120–130 nm). The prepared AgBr NPs were transformed to Ag NPs by the reduction using NaBH4. The sizes of the produced Ag NPs followed the same trends – the smallest NPs were produced in the presence of PEG and HEC polymers. Prepared AgBr and Ag NPs dispersions were tested for their biological activity. The obtained results of antimicrobial activity of AgBr and Ag NPs are discussed in terms of possible mechanism of the action of these NPs against tested microbial strains. The AgBr NPs are more effective against gram-negative bacteria and tested yeast strains while Ag NPs show the best antibacterial action against gram-positive bacteria strains. PMID:25781988

In situ Raman scattering study on a controllable plasmon-driven surface catalysis reaction on Ag nanoparticle arrays

International Nuclear Information System (INIS)

Dai, Z G; Xiao, X H; Zhang, Y P; Ren, F; Wu, W; Zhang, S F; Zhou, J; Jiang, C Z; Mei, F

2012-01-01

Control of the plasmon-driven chemical reaction for the transformation of 4-nitrobenzenethiol to p,p′-dimercaptoazobenzene by Ag nanoparticle arrays was studied. The Ag nanoparticle arrays were fabricated by means of nanosphere lithography. By changing the PS particle size, the localized surface plasmon resonance (LSPR) peaks of the Ag nanoparticle arrays can be tailored from 460 to 560 nm. The controlled reaction process was monitored by in situ surface-enhanced Raman scattering. The reaction can be dramatically influenced by varying the duration of laser exposure, Ag nanoparticle size, laser power and laser excitation wavelength. The maximum reaction speed was achieved when the LSPR wavelength of the Ag nanoparticle arrays matched the laser excitation wavelength. The experimental results reveal that the strong LSPR can effectively drive the transfer of the ‘hot’ electrons that decay from the plasmon to the reactants. The experimental results were confirmed by theoretical calculations. (paper)

Sudden Disappearance of the First-Order Transition in β-Pyrochlore KOs2O6 under Low Pressure

Science.gov (United States)

Umeo, Kazunori; Kubo, Hirokazu; Yamaura, Jun-ichi; Hiroi, Zenji; Takabatake, Toshiro

2009-12-01

We report the first observation of the pressure effect on the first-order transition at Tp = 7.5 K in the β-pyrochlore oxide superconductor KOs2O6 by specific-heat measurement. The peak in the specific heat at Tp disappeared at a low pressure of 0.02 GPa. With increasing pressure up to 0.02 GPa, the coefficient of the T5 dependence of the specific heat increases by 30%. This finding implies that low-energy excitations of phonons are enhanced by the suppression of the first-order transition. However, the specific-heat jump at Tc is unchanged with pressure up to 1 GPa, indicating that the strong coupling superconductivity is rather robust under pressure.

Facile synthesis of Ag nanocubes of 30 to 70 nm in edge length with CF(3)COOAg as a precursor.

Science.gov (United States)

Zhang, Qiang; Li, Weiyang; Wen, Long-Ping; Chen, Jingyi; Xia, Younan

2010-09-03

This paper describes a new protocol to synthesize Ag nanocubes of 30 to 70 nm in edge length with the use of CF(3)COOAg as a precursor to elemental silver. By adding a trace amount of NaSH and HCl to the polyol synthesis, Ag nanocubes were obtained with good quality, high reproducibility, and on a scale up to 0.19 g per batch for the 70 nm Ag nanocubes. The Ag nanocubes were found to grow in size at a controllable pace over the course of synthesis. The linear relationship between the edge length of the Ag nanocubes and the position of localized surface plasmon resonance (LSPR) peak provides a simple method for finely tuning and controlling the size of the Ag nanocubes by monitoring the UV/Vis spectra of the reaction at different times.

Facile Synthesis of Ag Nanocubes of 30 to 70 nm in Edge Length with CF3COOAg as a Precursor

Science.gov (United States)

Zhang, Qiang; Li, Weiyang; Wen, Long-Ping; Chen, Jingyi; Xia, Younan

2010-01-01

This paper describes a new protocol for producing Ag nanocubes of 30 to 70 nm in edge length with the use of CF3COOAg as a precursor to elemental silver. By adding a trace amount of sodium hydrosulfide (NaHS) and hydrochloric acid (HCl) into the polyol synthesis, Ag nanocubes were obtained with good quality, high reproducibility, and on a scale up to 0.19 g per batch for the 70-nm Ag nanocubes. The Ag nanocubes were found to grow in size at a controllable pace over the course of synthesis. The linear relationship between the edge length of the Ag nanocubes and the position of localized surface plasmon resonance (LSPR) peak provides a simple method for finely tuning and controlling the size of the Ag nanocubes by monitoring the UV-vis spectra of the reaction at different times. PMID:20593441

Long-term spectroscopic monitoring of the Luminous Blue Variable AG Carinae

Science.gov (United States)

Stahl, O.; Jankovics, I.; Kovács, J.; Wolf, B.; Schmutz, W.; Kaufer, A.; Rivinius, Th.; Szeifert, Th.

2001-08-01

We have extensively monitored the Luminous Blue Variable AG Car (HD 94910) spectroscopically. Our data cover the years 1989 to 1999. In this period, the star underwent almost a full S Dor cycle from visual minimum to maximum and back. Over several seasons, up to four months of almost daily spectra are available. Our data cover most of the visual spectral range with a high spectral resolution (lambda /Delta lambda ~ 20 000). This allows us to investigate the variability in many lines on time scales from days to years. The strongest variability occurs on a time scale of years. Qualitatively, the variations can be understood as changes of the effective temperature and radius, which are in phase with the optical light curve. Quantitatively, there are several interesting deviations from this behaviour, however. The Balmer lines show P Cygni profiles and have their maximum strength (both in equivalent width and line flux) after the peak of the optical light curve, at the descending branch of the light curve. The line-width during maximum phase is smaller than during minimum, but it has a local maximum close to the peak of the visual light curve. We derive mass-loss rates over the cycle from the Hα line and find the highest mass loss rates (log dot {M}/({M}_sun yr-1) ~ -3.8, about a factor of five higher than in the minimum, where we find log dot {M}/({M}_sun yr-1) ~ -4.5) after the visual maximum. Line-splitting is very commonly observed, especially on the rise to maximum and on the descending branch from maximum. The components are very long-lived (years) and are probably unrelated to similar-looking line-splitting events in normal supergiants. Small apparent accelerations of the components are observed. The change in radial velocity could be due to successive narrowing of the components, with the absorption disappearing at small expansion velocities first. In general, the line-splitting is more likely the result of missing absorption at intermediate velocities than of

Influence of different preparation conditions on catalytic activity of ag /gama-al/sub 2/o/sub 3/ for hydrogenation of coal slime pyrolysis

International Nuclear Information System (INIS)

Lei, Z.; Rong, C.

2014-01-01

This paper, introducing variable conditional factors with Ag/AL/sub 2/O/sub 3/ as catalyst, selects five variables to investigate the influences of experimental conditions on Ag/Al2O/sub 3/ catalytic activity and define the optimal process conditions. These variables include Ag loading amount, calcinations temperature, calcinations time, reduction temperature, reduction time. X ray diffraction (XRD), hydrogen temperature-programmed reduction (TPR), X ray photoelectron spectrum (XPS) and scanning electron microscopy (SEM) were utilized to characterize the catalytic activity of Ag/-Al/sub 2/O/sub 3/, active center structure and state and those of carrier were emphatically studied, In the meantime the effects of active center and carrier on catalytic activity are studied. The results showed that: (1) In the range of 600 degree C-900 degree C, the catalytic activity of Ag/-Al/sub 2/O/sub 3/ with different loading showed little difference when changing loading amount, in the range of 900 degree C-1100 degree C, when the loading was 5%, the catalytic activity was very high; From the XRD and SEM characterizations, when the loading was 5%, it showed strong intensity diffraction peak of Ag crystal, crystal Ag is the most important activity center to promote hydrogen yield. (2) the catalytic activity of Ag/-Al/sub 2/O/sub 3/ at 450 degree C was considerably higher than that at 400 degree C and 500 degree C. By BET, XRD and SEM characterization, it can be seen, the diffraction peaks intensity of Ag crystal at 450 degree C is higher and sharper than that at 400 degree C and 500 degree C and with the increase of calcinations temperature, the specific surface area of catalysts also increased. (3) In the range of 600 degree C - 1000 degree C, the effects of calcinations time can be negligible, while, with temperature higher than 1000 degree C, 4-hour-calcinations-time catalyst exhibits a more noticeable catalytic activity than 3-hour and 5-hour catalyst do; From the XRD

AgI/Ag3PO4 hybrids with highly efficient visible-light driven photocatalytic activity

International Nuclear Information System (INIS)

Katsumata, Hideyuki; Hayashi, Takahiro; Taniguchi, Masanao; Suzuki, Tohru; Kaneco, Satoshi

2015-01-01

Highlights: • AgI/Ag 3 PO 4 hybrid was prepared via an in situ anion-exchange method. • AgI/Ag 3 PO 4 displays the excellent photocatalytic activity under visible light. • AgI/Ag 3 PO 4 readily transforms to be Ag@AgI/Ag 3 PO 4 system. • h + and O 2 ·− play the major role in the AO 7 decolorization over AgI/Ag 3 PO 4 . • The activity enhancement is ascribed to a Z-scheme system composed of Ag 3 PO 4 , Ag and AgI. - Abstract: Highly efficient visible-light-driven AgI/Ag 3 PO 4 hybrid photocatalysts with different mole ratios of AgI were prepared via an in situ anion-exchange method and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), UV–vis diffuse reflectance spectroscopy (DRS) and photoluminescence (PL) technique. Under visible light irradiation (>420 nm), the AgI/Ag 3 PO 4 photocatalysts displayed the higher photocatalytic activity than pure Ag 3 PO 4 and AgI for the decolorization of acid orange 7 (AO 7). Among the hybrid photocatalysts, AgI/Ag 3 PO 4 with 80% of AgI exhibited the highest photocatalytic activity for the decolorization of AO 7. X-ray photoelectron spectroscopy (XPS) results revealed that AgI/Ag 3 PO 4 readily transformed to be Ag@AgI/Ag 3 PO 4 system while the photocatalytic activity of AgI/Ag 3 PO 4 remained after 5 recycling runs. In addition, the quenching effects of different scavengers displayed that the reactive h + and O 2 ·− play the major role in the AO 7 decolorization. The photocatalytic activity enhancement of AgI/Ag 3 PO 4 hybrids can be ascribed to the efficient separation of electron–hole pairs through a Z-scheme system composed of Ag 3 PO 4 , Ag and AgI, in which Ag nanoparticles act as the charge separation center

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 ...

Homogeneous synthesis of Ag nanoparticles-doped water-soluble cellulose acetate for versatile applications.

Science.gov (United States)

Cao, Jie; Sun, Xunwen; Zhang, Xinxing; Lu, Canhui

2016-11-01

We report a facile and efficient approach for synthesis of well-dispersed and stable silver nanoparticles (Ag NPs) using water-soluble cellulose acetate (CA) as both reductant and stabilizer. Partially substituted CA with highly active hydroxyl groups and excellent water-solubility is able to reduce silver ions in homogeneous aqueous medium effectively. The synthesized Ag NPs were characterized by UV-vis spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy and energy dispersive X-ray spectroscope analysis. The as-prepared Ag NPs were well-dispersed, showing a surface plasmon resonance peak at 426nm. The resulted Ag NPs@CA nanohybrids exhibit high catalytic activity for the reduction of 4-nitrophenol to 4-aminophenol in the presence of NaBH 4 . Meanwhile, the nanohybrids are also effective in inhibiting the growth of bacterial. This environmentally friendly method promotes the use of renewable natural resources to prepare a variety of inorganic-organic materials for catalysis, antibacterial, sensors and other applications. Copyright © 2016 Elsevier B.V. All rights reserved.

Thermal design studies in superconducting rf cavities: Phonon peak and Kapitza conductance

Directory of Open Access Journals (Sweden)

A. Aizaz

2010-09-01

Full Text Available Thermal design studies of superconducting radio frequency (SRF cavities involve two thermal parameters, namely the temperature dependent thermal conductivity of Nb at low temperatures and the heat transfer coefficient at the Nb-He II interface, commonly known as the Kapitza conductance. During the fabrication process of the SRF cavities, Nb sheet is plastically deformed through a deep drawing process to obtain the desired shape. The effect of plastic deformation on low temperature thermal conductivity as well as Kapitza conductance has been studied experimentally. Strain induced during the plastic deformation process reduces the thermal conductivity in its phonon transmission regime (disappearance of phonon peak by 80%, which may explain the performance limitations of the defect-free SRF cavities during their high field operations. Low temperature annealing of the deformed Nb sample could not recover the phonon peak. However, moderate temperature annealing during the titanification process recovered the phonon peak in the thermal conductivity curve. Kapitza conductance measurements for the Nb-He II interface for various surface topologies have also been carried out before and after the annealing. These measurements reveal consistently increased Kapitza conductance after the annealing process was carried out in the two temperature regimes.

A Solid-State Thin-Film Ag/AgCl Reference Electrode Coated with Graphene Oxide and Its Use in a pH Sensor

Directory of Open Access Journals (Sweden)

Tae Yong Kim

2015-03-01

Full Text Available In this study, we describe a novel solid-state thin-film Ag/AgCl reference electrode (SSRE that was coated with a protective layer of graphene oxide (GO. This layer was prepared by drop casting a solution of GO on the Ag/AgCl thin film. The potential differences exhibited by the SSRE were less than 2 mV for 26 days. The cyclic voltammograms of the SSRE were almost similar to those of a commercial reference electrode, while the diffusion coefficient of Fe(CN63− as calculated from the cathodic peaks of the SSRE was 6.48 × 10−6 cm2/s. The SSRE was used in conjunction with a laboratory-made working electrode to determine its suitability for practical use. The average pH sensitivity of this combined sensor was 58.5 mV/pH in the acid-to-base direction; the correlation coefficient was greater than 0.99. In addition, an integrated pH sensor that included the SSRE was packaged in a secure digital (SD card and tested. The average sensitivity of the chip was 56.8 mV/pH, with the correlation coefficient being greater than 0.99. In addition, a pH sensing test was also performed by using a laboratory-made potentiometer, which showed a sensitivity of 55.4 mV/pH, with the correlation coefficient being greater than 0.99.

A solid-state thin-film Ag/AgCl reference electrode coated with graphene oxide and its use in a pH sensor.

Science.gov (United States)

Kim, Tae Yong; Hong, Sung A; Yang, Sung

2015-03-17

In this study, we describe a novel solid-state thin-film Ag/AgCl reference electrode (SSRE) that was coated with a protective layer of graphene oxide (GO). This layer was prepared by drop casting a solution of GO on the Ag/AgCl thin film. The potential differences exhibited by the SSRE were less than 2 mV for 26 days. The cyclic voltammograms of the SSRE were almost similar to those of a commercial reference electrode, while the diffusion coefficient of Fe(CN)63- as calculated from the cathodic peaks of the SSRE was 6.48 × 10-6 cm2/s. The SSRE was used in conjunction with a laboratory-made working electrode to determine its suitability for practical use. The average pH sensitivity of this combined sensor was 58.5 mV/pH in the acid-to-base direction; the correlation coefficient was greater than 0.99. In addition, an integrated pH sensor that included the SSRE was packaged in a secure digital (SD) card and tested. The average sensitivity of the chip was 56.8 mV/pH, with the correlation coefficient being greater than 0.99. In addition, a pH sensing test was also performed by using a laboratory-made potentiometer, which showed a sensitivity of 55.4 mV/pH, with the correlation coefficient being greater than 0.99.

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

Field determination of bacterial disappearance in seawater

DEFF Research Database (Denmark)

Harremoës, Poul

1970-01-01

The article presents two approaches to field determination of disappearance of viable, fecal bacteria after discharge with sewage into a marine environment. The first approach is based on simultaneous sampling for bacterial counting and monitoring of dilution using a conservative tracer, which is...

SIMULATIONS OF THE AGS MMPS STORING ENERGY IN CAPACITOR BANKS

Energy Technology Data Exchange (ETDEWEB)

MARNERIS,I.; BADEA, V.S.; BONATI, R.; ROSER, T.; SANDBERG, J.

2007-06-25

The Brookhaven AGS Main Magnet Power Supply (MMPS) is a thyristor control supply rated at 5500 Amps, +/-9000 Volts. The peak magnet power is 50 MWatts. The power supply is fed from a motor/generator manufactured by Siemens. The generator is 3 phase 7500 Volts rated at 50 MVA. The peak power requirements come from the stored energy in the rotor of the motor/generator. The motor generator is about 45 years old, made by Siemens and it is not clear if companies will be manufacturing similar machines in the future. We are therefore investigating different ways of storing energy for future AGS MMPS operations. This paper will present simulations of a power supply where energy is stored in capacitor banks. Two dc to dc converters will be presented along with the control system of the power section. The switching elements will be IGCT's made by ABB. The simulation program used is called PSIM version 6.1. The average power from the local power authority into the power supply will be kept constant during the pulsing of the magnets at +/-50 MW. The reactive power will also be kept constant below 1.5 MVAR. Waveforms will be presented.

Photocatalytic oxidation removal of Hg"0 using ternary Ag/AgI-Ag_2CO_3 hybrids in wet scrubbing process under fluorescent light

International Nuclear Information System (INIS)

Zhang, Anchao; Zhang, Lixiang; Chen, Xiaozhuan; Zhu, Qifeng; Liu, Zhichao; Xiang, Jun

2017-01-01

Highlights: • Ag/AgI-Ag_2CO_3 hybrids were employed for Hg"0 removal under fluorescent light. • Superoxide radical (·O_2"−) played a key role in Hg"0 removal. • NO exhibited a significant effect on Hg"0 removal in comparison to SO_2. • The mechanism for enhanced Hg"0 removal over Ag/AgI-Ag_2CO_3 was proposed. - Abstract: A series of ternary Ag/AgI-Ag_2CO_3 photocatalysts synthesized using a facile coprecipitation method were employed to investigate their performances of Hg"0 removal in a wet scrubbing reactor. The hybrids were characterized by N_2 adsorption-desorption, XRD, SEM-EDS, HRTEM, XPS, DRS and ESR. The photocatalytic activities of Hg"0 removal were evaluated under fluorescent light. The results showed that AgI content, fluorescent light irradiation, reaction temperature all showed significant influences on Hg"0 removal. NO exhibited significant effect on Hg"0 removal in comparison to SO_2. Among these ternary Ag/AgI-Ag_2CO_3 hybrids, Ag/AgI(0.1)-Ag_2CO_3 showed the highest Hg"0 removal efficiency, which could be ascribed to the effective separation of photogenerated electron-hole pairs between AgI and Ag_2CO_3 and the surface plasmon resonance (SPR) effect in the visible region by metallic silver nanoparticles (Ag"0 NPs). The trapping studies of reactive radicals showed that the superoxide radicals (·O_2"−) may play a key role in Hg"0 removal under fluorescent light. According to the experimental and characterization results, a possible photocatalytic oxidation mechanism for enhanced Hg"0 removal over Ag/AgI(0.1)-Ag_2CO_3 hybrid under fluorescent light was proposed.

Occurrence, characterisation and fate of (nano)particulate Ti and Ag in two Norwegian wastewater treatment plants

DEFF Research Database (Denmark)

Polesel, Fabio; Farkas, Julia; Kjos, Marianne

2018-01-01

was conducted in two full-scale WWTPs in Trondheim (Norway) employing only primary treatment. We assessed the occurrence and elimination of Ti and Ag, and conducted size-based fractionation using sequential filtration of influent samples to separate particulate, colloidal and dissolved fractions. Eight...... concentration patterns (especially total suspended solids), with peaks during the morning and/or evening and minima at night, indicating household discharges as predominant source. Irregular profiles were exhibited by influent Ag, with periodic concentration spikes suggesting short-term discharges from one...

Ag ion irradiated based sensor for the electrochemical determination of epinephrine and 5-hydroxytryptamine in human biological fluids

Energy Technology Data Exchange (ETDEWEB)

Goyal, Rajendra N., E-mail: rngcyfcy@iitr.ernet.in [Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee 247667 (India); Agrawal, Bharati [Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee 247667 (India)

2012-09-19

Highlights: Black-Right-Pointing-Pointer Ag ions irradiation enhances the electrocatalytic activity of carbon nano tubes. Black-Right-Pointing-Pointer The low fluence of irradiation caused the ordering of carbon nano tubes. Black-Right-Pointing-Pointer Simultaneous determination of epinephrine and 5-hydroxytryptamine has been carried out. Black-Right-Pointing-Pointer The determination of the neurotransmitters in human blood and urine is reported. - Abstract: A promising and highly sensitive voltammetric method has been developed for the first time for the determination of epinephrine (EP) and 5-hydroxytryptamine (5-HT) using 120 MeV Ag ion irradiated multi-walled carbon nano tube (MWCNT) based sensor. The MWCNT were irradiated at various fluences of 1e12, 3e12 and 1e13 ions cm{sup -2} using palletron accelerator. The simultaneous determination of EP and 5-HT has been carried out in phosphate buffer solution of pH 7.20 using square wave voltammetry and cyclic voltammetry. Experimental results suggested that irradiation of MWCNT by Ag ions enhanced the electrocatalytic activity due to increase in effective surface area and insertion of Ag ions, leading to a remarkable enhancement in peak currents and shift of peak potentials to less positive values as compared to the unirradiated MWCNT (pristine). The developed sensor exhibited a linear relationship between peak current and concentration of EP and 5-HT in the range 0.1-105 {mu}M with detection limit (3{sigma}/b) of 2 nM and 0.75 nM, respectively. The practical utility of irradiation based MWCNT sensor has been demonstrated for the determination of EP and 5-HT in human urine and blood samples.

RRR and thermal conductivity of Ag and Ag0.2wt%Mg alloy in Ag/Bi-2212 wires

Energy Technology Data Exchange (ETDEWEB)

Li, Pei [Fermilab; Ye, L. [North Carolina State U.; Jiang. J., Jiang. J. [Natl. High Mag. Field Lab.; Shen, T. [Fermilab

2015-08-19

The residual resistivity ratio (RRR) and thermal conductivity of metal matrix in metal/superconductor composite wires are important parameters for designing superconducting magnets. However, the resistivity of silver in reacted Ag/Bi-2212 wires has yet to be determined over temperature range from 4.2 K to 80 K because Bi-2212 filaments have a critical transition temperature Tc of ~ 80 K, and because it is unknown whether the RRR of Ag/Bi-2212 degrades with Cu diffusing from Bi-2212 filaments into silver sheathes at elevated temperatures and to what degree it varies with heat treatment. We measured the resistivity of stand-alone Ag and AgMg (Ag-0.2wt%Mg) wires as well as the resistivity of Ag and Ag- 0.2wt%Mg in the state-of-the-art Ag/Bi-2212 round wires reacted in 1 bar oxygen at 890 °C for 1, 8, 24 and 48 hours and quickly cooled to room temperature. The heat treatment was designed to reduce the critical current Ic of Bi-2212 wires to nearly zero while allowing Cu loss to fully manifest itself. We determined that pure silver exhibits a RRR of ~ 220 while the oxide-dispersion strengthened AgMg exhibits a RRR of ~ 5 in stand-alone samples. A surprising result is that the RRR of silver in the composite round wires doesn’t degrade with extended time at 890 °C for up to 48 hours. This surprising result may be explained by our observation that the Cu that diffuses into the silver tends to form Cu2O precipitates in oxidizing atmosphere, instead of forming Ag-Cu solution alloy. We also measured the thermal conductivity and the magneto-resistivity of pure Ag and Ag-0.2 wt%Mg from 4.2 K to 300 K in magnetic fields up to 14.8 T and summarized them using a Kohler plot.

Synthesis, morphological control, and antibacterial properties of hollow/solid Ag2S/Ag heterodimers

KAUST Repository

Pang, Maolin

2010-08-11

Ag2S and Ag are important functional materials that have received considerable research interest in recent years. In this work, we develop a solution-based synthetic method to combine these two materials into hollow/solid Ag2S/Ag heterodimers at room temperature. Starting from monodisperse Cu2O solid spheres, CuS hollow spheres can be converted from Cu2O through a modified Kirkendall process, and the obtained CuS can then be used as a solid precursor for preparation of the Ag2S/Ag heterodimers through ion exchange and photo-assisted reduction. We have found that formation of the Ag2S/Ag heterodimers is instantaneous, and the size of Ag nanocrystals on the hollow spheres of Ag2S can be controlled by changing the concentration and power of reducing agents in the synthesis. The growth of Ag nanoparticles on hollow spheres of Ag2S in the dimers is along the [111] direction of the silver crystal; the light absorption properties have also been investigated. Furthermore, coupling or tripling of Ag2S/Ag heterodimers into dumbbell-like trimers ((Ag 2S)2/Ag, linear) and triangular tetramers ((Ag 2S)3/Ag, coplanar) can also be attained at 60°C by adding the bidentate ligand ethylenediamine as a cross-linking agent. To test the applicability of this highly asymmetric dipolar composite, photocatalytic inactivation of Escherichia coli K-12 in the presence of the as-prepared Ag 2S/Ag heterodimers has been carried out under UV irradiation. The added Ag2S/Ag heterodimers show good chemical stability under prolonged UV irradiation, and no appreciable solid dissolution is found. Possible mechanisms regarding the enhanced antibacterial activity have also been addressed. © 2010 American Chemical Society.

Transformation from Ag@Ag{sub 3}PO{sub 4} to Ag@Ag{sub 2}SO{sub 4} hybrid at room temperature: preparation and its visible light photocatalytic activity

Energy Technology Data Exchange (ETDEWEB)

Wei, Ting; Gao, Shanmin, E-mail: gaosm@ustc.edu; Wang, Qingyao; Xu, Hui [Ludong University, College of Chemistry and Materials Science (China); Wang, Zeyan; Huang, Baibiao, E-mail: bbhuang@sdu.edu.cn; Dai, Ying [Shandong University, State Key Laboratory of Crystal Materials (China)

2017-02-15

In the present study, Ag/Ag{sub 2}SO{sub 4} hybrid photocatalysts were obtained via a facile redox–precipitation reaction approach by using Ag@Ag{sub 3}PO{sub 4} nanocomposite as the precursor and KMnO{sub 4} as the oxidant. Multiple techniques, such as X-ray diffraction pattern (XRD), transmission electron microscope (TEM), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), UV–vis diffuse reflectance spectroscopy (DRS) and Brunauer–Emmett–Teller (BET), photocurrent and electrochemical impedance spectroscopy (EIS), were applied to investigate the structures, morphologies, optical, and electronic properties of as-prepared samples. The photocatalytic activities were evaluated by photodegradation of organic rhodamine B (RhB) and methyl orange (MO) under visible light irradiation. It was found that pure Ag{sub 2}SO{sub 4} can partially transform into metallic Ag during the photocatalytic degradation of organic pollutants, but the Ag/Ag{sub 2}SO{sub 4} hybrids can maintain its structure stability and show enhanced visible light photocatalytic activity because of the surface plasma resonance effect of the metallic Ag.

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.

Nano-silver mediated polymerization of pyrrole: synthesis and gas sensing properties of polypyrrole (PPy)/Ag nano-composite.

Science.gov (United States)

Kate, Kunal H; Damkale, Shubhangi R; Khanna, P K; Jain, G H

2011-09-01

Thermal polymerization of pyrrole was performed using silver nitrate as source of silver ions followed by its conversion to Polypyrrole (PPy)/Ag nano-comoposites without using any external oxidizing agent or solvent. The formation of PPy was monitored by UV-Visible absorption spectroscopy showing a band at approximately 464 nm. XRD measurement confirmed characteristic peaks for face centered cubic (fcc) silver and presence of PPy at 2 theta of approximately 23 degrees suggesting the formation of PPy/Ag nanocomposite. Transmission electron microscopy (TEM) images showed non-aggregated spherical Ag nano-particles of about 5-10 nm. PPy/Ag thick film acts as a NH3 sensor at 100 degrees C, a H2S sensor at 250 degrees C and CO2 sensor at 350 degrees C. The thick films showed capability to recognize various gases at different operating temperature.

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.

Core/shell AgNi/PtAgNi nanoparticles as methanol-tolerant oxygen reduction electrocatalysts

International Nuclear Information System (INIS)

Wu, Dengfeng; Cheng, Daojian

2015-01-01

A core/shell AgNi/PtAgNi nanoparticle (NP) was synthesized via a new seed-mediated growth method in organic solvent medium. The as-synthesized AgNi/PtAgNiNP exhibits an AgNi core coated with PtAgNi shell, which was confirmed by transmission electron microscopy (TEM), ultraviolet–visible absorption spectroscopy and X-ray Photoelectron Spectroscopy (XPS). The AgNi/PtAgNiNPs/C catalyst possesses higher oxygen reduction reaction (ORR) activity and better durability compared with the commercial Pt/C catalyst. It is found that the ORR polarization curve of the AgNi/PtAgNiNPs/C catalyst shows an onset potential of 0.91 V vs. RHE, which is superior to the commercial Pt/C (0.88 V vs. RHE). In addition, the AgNi/PtAgNiNPs/C catalyst shows much better durability than the commercial Pt/C catalyst. More interestingly, the AgNi/PtAgNiNPs/C catalyst displays much higher methanol tolerance than the commercial Pt/C catalyst in 0.1 M KOH solution in the presence of 0.5 M methanol. Our results show that core/shell AgNi/PtAgNiNPs possess selective activity for ORR even in the presence of methanol, showing potential application as methanol-tolerant cathode catalysts in direct methanol fuel cells.

Development of a Rhizoctonia solani AG1-IB Specific Gene Model Enables Comparative Genome Analyses between Phytopathogenic R. solani AG1-IA, AG1-IB, AG3 and AG8 Isolates.

Directory of Open Access Journals (Sweden)

Daniel Wibberg

Full Text Available Rhizoctonia solani, a soil-born plant pathogenic basidiomycetous fungus, affects various economically important agricultural and horticultural crops. The draft genome sequence for the R. solani AG1-IB isolate 7/3/14 as well as a corresponding transcriptome dataset (Expressed Sequence Tags--ESTs were established previously. Development of a specific R. solani AG1-IB gene model based on GMAP transcript mapping within the eukaryotic gene prediction platform AUGUSTUS allowed detection of new genes and provided insights into the gene structure of this fungus. In total, 12,616 genes were recognized in the genome of the AG1-IB isolate. Analysis of predicted genes by means of different bioinformatics tools revealed new genes whose products potentially are involved in degradation of plant cell wall components, melanin formation and synthesis of secondary metabolites. Comparative genome analyses between members of different R. solani anastomosis groups, namely AG1-IA, AG3 and AG8 and the newly annotated R. solani AG1-IB genome were performed within the comparative genomics platform EDGAR. It appeared that only 21 to 28% of all genes encoded in the draft genomes of the different strains were identified as core genes. Based on Average Nucleotide Identity (ANI and Average Amino-acid Identity (AAI analyses, considerable sequence differences between isolates representing different anastomosis groups were identified. However, R. solani isolates form a distinct cluster in relation to other fungi of the phylum Basidiomycota. The isolate representing AG1-IB encodes significant more genes featuring predictable functions in secondary metabolite production compared to other completely sequenced R. solani strains. The newly established R. solani AG1-IB 7/3/14 gene layout now provides a reliable basis for post-genomics studies.

AGS experiments - 1994, 1995, 1996

Energy Technology Data Exchange (ETDEWEB)

Depken, J.C.

1997-01-01

This report contains the following information on the Brookhaven AGS Accelerator complex: FY 1996 AGS schedule as run; FY 1997 AGS schedule (working copy); AGS beams 1997; AGS experimental area FY 1994 physics program; AGS experimental area FY 1995 physics program; AGS experimental area FY 1996 physics program; AGS experimental area FY 1997 physics program (in progress); a listing of experiments by number; two-phage summaries of each experiment begin here, also ordered by number; listing of publications of AGS experiments begins here; and listing of AGS experimenters begins here.

AGS experiments - 1994, 1995, 1996

International Nuclear Information System (INIS)

Depken, J.C.

1997-01-01

This report contains the following information on the Brookhaven AGS Accelerator complex: FY 1996 AGS schedule as run; FY 1997 AGS schedule (working copy); AGS beams 1997; AGS experimental area FY 1994 physics program; AGS experimental area FY 1995 physics program; AGS experimental area FY 1996 physics program; AGS experimental area FY 1997 physics program (in progress); a listing of experiments by number; two-phage summaries of each experiment begin here, also ordered by number; listing of publications of AGS experiments begins here; and listing of AGS experimenters begins here

AGS experiments -- 1991, 1992, 1993

International Nuclear Information System (INIS)

Depken, J.C.

1994-04-01

This report contains: (1) FY 1993 AGS schedule as run; (2) FY 1994--95 AGS schedule; (3) AGS experiments ≥ FY 1993 (as of 30 March 1994); (4) AGS beams 1993; (5) AGS experimental area FY 1991 physics program; (6) AGS experimental area FY 1992 physics program; (7) AGS experimental area FY 1993 physics program; (8) AGS experimental area FY 1994 physics program (planned); (9) a listing of experiments by number; (10) two-page summaries of each experiment; (11) listing of publications of AGS experiments; and (12) listing of AGS experiments

3D Evolution of a Filament Disappearance Event Observed by STEREO

Science.gov (United States)

Gosain, S.; Schmieder, B.; Venkatakrishnan, P.; Chandra, R.; Artzner, G.

2009-10-01

A filament disappearance event was observed on 22 May 2008 during our recent campaign JOP 178. The filament, situated in the Southern Hemisphere, showed sinistral chirality consistent with the hemispheric rule. The event was well observed by several observatories, in particular by THEMIS. One day, before the disappearance, Hα observations showed up- and down-flows in adjacent locations along the filament, which suggest plasma motions along twisted flux rope. THEMIS and GONG observations show shearing photospheric motions leading to magnetic flux canceling around barbs. STEREO A, B spacecraft with separation angle 52.4°, showed quite different views of this untwisting flux rope in He ii 304 Å images. Here, we reconstruct the three-dimensional geometry of the filament during its eruption phase using STEREO EUV He ii 304 Å images and find that the filament was highly inclined to the solar normal. The He ii 304 Å movies show individual threads, which oscillate and rise to an altitude of about 120 Mm with apparent velocities of about 100 km s-1 during the rapid evolution phase. Finally, as the flux rope expands into the corona, the filament disappears by becoming optically thin to undetectable levels. No CME was detected by STEREO, only a faint CME was recorded by LASCO at the beginning of the disappearance phase at 02:00 UT, which could be due to partial filament eruption. Further, STEREO Fe xii 195 Å images showed bright loops beneath the filament prior to the disappearance phase, suggesting magnetic reconnection below the flux rope.

Investigation on the morphological and optical evolution of bimetallic Pd-Ag nanoparticles on sapphire (0001) by the systematic control of composition, annealing temperature and time.

Science.gov (United States)

Pandey, Puran; Kunwar, Sundar; Sui, Mao; Bastola, Sushil; Lee, Jihoon

2017-01-01

Multi-metallic alloy nanoparticles (NPs) can offer additional opportunities for modifying the electronic, optical and catalytic properties by the control of composition, configuration and size of individual nanostructures that are consisted of more than single element. In this paper, the fabrication of bimetallic Pd-Ag NPs is systematically demonstrated via the solid state dewetting of bilayer thin films on c-plane sapphire by governing the temperature, time as well as composition. The composition of Pd-Ag bilayer remarkably affects the morphology of alloy nanostructures, in which the higher Ag composition, i.e. Pd0.25Ag0.75, leads to the enhanced dewetting of bilayers whereas the higher Pd composition (Pd0.75Ag0.25) hinders the dewetting. Depending on the annealing temperature, Pd-Ag alloy nanostructures evolve with a series of configurations, i.e. nucleation of voids, porous network, elongated nanoclusters and round alloy NPs. In addition, with the annealing time set, the gradual configuration transformation from the elongated to round alloy NPs as well as size reduction is demonstrated due to the enhanced diffusion and sublimation of Ag atoms. The evolution of various morphology of Pd-Ag nanostructures is described based on the surface diffusion and inter-diffusion of Pd and Ag adatoms along with the Ag sublimation, Rayleigh instability and energy minimization mechanism. The reflectance spectra of bimetallic Pd-Ag nanostructures exhibit various quadrupolar and dipolar resonance peaks, peak shifts and absorption dips owing to the surface plasmon resonance of nanostructures depending on the surface morphology. The intensity of reflectance spectra is gradually decreased along with the surface coverage and NP size evolution. The absorption dips are red-shifted towards the longer wavelength for the larger alloy NPs and vice-versa.

Investigation on the morphological and optical evolution of bimetallic Pd-Ag nanoparticles on sapphire (0001 by the systematic control of composition, annealing temperature and time.

Directory of Open Access Journals (Sweden)

Puran Pandey

Full Text Available Multi-metallic alloy nanoparticles (NPs can offer additional opportunities for modifying the electronic, optical and catalytic properties by the control of composition, configuration and size of individual nanostructures that are consisted of more than single element. In this paper, the fabrication of bimetallic Pd-Ag NPs is systematically demonstrated via the solid state dewetting of bilayer thin films on c-plane sapphire by governing the temperature, time as well as composition. The composition of Pd-Ag bilayer remarkably affects the morphology of alloy nanostructures, in which the higher Ag composition, i.e. Pd0.25Ag0.75, leads to the enhanced dewetting of bilayers whereas the higher Pd composition (Pd0.75Ag0.25 hinders the dewetting. Depending on the annealing temperature, Pd-Ag alloy nanostructures evolve with a series of configurations, i.e. nucleation of voids, porous network, elongated nanoclusters and round alloy NPs. In addition, with the annealing time set, the gradual configuration transformation from the elongated to round alloy NPs as well as size reduction is demonstrated due to the enhanced diffusion and sublimation of Ag atoms. The evolution of various morphology of Pd-Ag nanostructures is described based on the surface diffusion and inter-diffusion of Pd and Ag adatoms along with the Ag sublimation, Rayleigh instability and energy minimization mechanism. The reflectance spectra of bimetallic Pd-Ag nanostructures exhibit various quadrupolar and dipolar resonance peaks, peak shifts and absorption dips owing to the surface plasmon resonance of nanostructures depending on the surface morphology. The intensity of reflectance spectra is gradually decreased along with the surface coverage and NP size evolution. The absorption dips are red-shifted towards the longer wavelength for the larger alloy NPs and vice-versa.

Ag nanoparticle effects on the thermoluminescent properties of monoclinic ZrO2 exposed to ultraviolet and gamma radiation

International Nuclear Information System (INIS)

Villa-Sanchez, G; Mendoza-Anaya, D; Gutierrez-Wing, C; Perez-Hernandez, R; Gonzalez-MartInez, P R; Angeles-Chavez, C

2007-01-01

The goal of this work was to analyse ZrO 2 in the pure state and when doped with Ag nanoparticles, by electron microscopy, x-ray diffraction and thermoluminescence methods. According to the results obtained, Ag nanoparticles did not modify the morphology or the crystalline structure of the ZrO 2 . The thermoluminescent (TL) response of pure ZrO 2 showed two peaks, one at 334 K and the other at 417 K, when it was exposed to ultraviolet (UV) radiation, and at 342 and 397 K when gamma radiation was used. For ZrO 2 impregnated with Ag nanoparticles a diminished TL intensity due to nanoparticle shielding was observed, but the glow curve shape was similar. However, when Ag nanoparticles were added during the ZrO 2 synthesis, a shift of the TL peaks towards higher temperature values with reference to pure ZrO 2 was observed. A linear dependence of the integrated TL signal as a function of the irradiation dose was observed in all analysed samples. It was possible to determine some kinetic parameters, such as activation energy, kinetic order and frequency factor, using the sequential quadratic programming glow curve deconvolution; it was found that these values are highly dependent on the type of radiation used. Ag nanoparticles present in ZrO 2 also modified the kinetic parameters, mainly when they were added during the synthesis of ZrO 2 . Our results reinforce the possibilities of using pure and doped ZrO 2 as an appropriate dosimetric material in radiation physics

Alloying of Yb-Cu and Yb-Ag utilizing liquid ammonia metal solutions of ytterbium

International Nuclear Information System (INIS)

Imamura, H.; Yoshimura, T.; Sakata, Y.

2003-01-01

In the course of the studies on preparation of novel compounds using the dissolution of Eu or Yb metals in liquid ammonia, the formation of Yb-Cu and Yb-Ag intermetallic films has been found. When Cu or Ag metal powders were placed in a reactor containing a solution of Yb metal in liquid ammonia, the dissolved Yb readily react with the Cu or Ag metal particles to form surface alloy compounds. X-ray diffraction of Yb-Cu showed that upon thermal treatment above 673 K, the Yb metal deposited on the Cu particles reacted together to be transformed into the YbCu 6.5 intermetallic compound. A characteristic endothermic peak at 749 K, due to alloying of Yb-Cu, was observed by the differential scanning calorimeter measurements. By use of the high reactivity of liquid ammonia metal solutions of ytterbium, it was found that the ytterbium intermetallic films were readily formed under mild conditions. Yb-Cu and Yb-Ag exhibited enhanced catalytic activity for the hydrogenation of ethene as a result of alloying

A search for muon neutrino and antineutrino disappearance in the Booster Neutrino Beam

Energy Technology Data Exchange (ETDEWEB)

Mahn, Kendall Brianna McConnel [Columbia Univ., New York, NY (United States)

2009-04-01

This dissertation presents a search for v_μ and $\\bar{v}$_μ disappearance with the MiniBooNE experiment in the Δm² region of a few eV². Disappearance measurements in this oscillation region constrain sterile neutrino models and CPT violation in the lepton sector. Fits to the shape of the v_μ and $\\bar{v}$_μ energy spectra reveal no evidence for disappearance in either mode. This is the first test of $\\bar{v}$_μ disappearance between Δm² = 0.1 - 10 eV². In addition, prospects for performing a joint analysis using the SciBooNE detector in conjunction with MiniBooNE are discussed.

Sensitive electrochemical sensor of tryptophan based on Ag-C core–shell nanocomposite modified glassy carbon electrode

International Nuclear Information System (INIS)

Mao Shuxian; Li Weifeng; Long Yumei; Tu Yifeng; Deng, Anping

2012-01-01

Graphical abstract: Ag-C and Colloidal carbon sphere modified glassy carbon electrodes were prepared. It was clear that the Ag-C/GCE exhibited enhanced electrocatalytic activity towards Trp, which could result from the synergistic effect between Ag core and carbon shell. The Ag-C/GCE showed excellent analytical properties in the determination of Trp. Highlights: ► The electrochemical behavior of Ag-C core–shell nanocomposite was firstly proposed. ► Ag-C/GC electrode exhibited favorable electrocatalytic properties towards Trp. ► The good electrocatalysis was due to the synergistic effect of Ag-core and C-shell. ► The Ag-C/GC electrode displayed excellent analytical properties in determining Trp. - Abstract: We here reported a simple electrochemical method for the detection of tryptophan (Trp) based on the Ag-C modified glassy carbon (Ag-C/GC) electrode. The Ag-C core–shell structured nanoparticles were synthesized using one-pot hydrothermal method and characterized by scanning electron microscope (SEM), transmission electron microscope (TEM), and Fourier transform-infrared spectroscopy (FTIR). The electrochemical behaviors of Trp on Ag-C/GC electrode were investigated and exhibited a direct electrochemical process. The favorable electrochemical properties of Ag-C/GC electrode were attributed to the synergistic effect of the Ag core and carbon shell. The carbon shell cannot only protect Ag core but also contribute to the enhanced substrate accessibility and Trp-substrate interactions, while nano-Ag core can display good electrocatalytic activity to Trp at the same time. Under the optimum experimental conditions the oxidation peak current was linearly dependent on the Trp concentration in the range of 1.0 × 10 −7 to 1.0 × 10 −4 M with a detection limit of 4.0 × 10 −8 M (S/N = 3). In addition, the proposed electrode was applied for the determination of Trp concentration in real samples and satisfactory results were obtained. The technique offers

The disappearance of flow

International Nuclear Information System (INIS)

Soff, S.; Hartnack, C.; Stoecker, H.; Greiner, W.

1995-01-01

We investigate the disappearance of collective flow in the reaction plane in heavy-ion collisions within a microscopic model (QMD). A systematic study of the impact parameter dependence is performed for the system Ca+Ca. The balance energy strongly increases with impact parameter. Momentum dependent interactions reduce the balance energies for intermediate impact parameters b∼4.5 fm. Dynamical negative flow is not visible in the laboratory frame but does exist in the contact frame for the heavy system Au+Au. For semi-peripheral collisions of Ca+Ca with b∼6.5 fm a new two-component flow is discussed. Azimuthal distributions exhibit strong collectiv flow signals, even at the balance energy. (orig.)

Thermodynamic properties of solid solutions in the system Ag2S–Ag2Se

International Nuclear Information System (INIS)

Pal’yanova, G.A.; Chudnenko, K.V.; Zhuravkova, T.V.

2014-01-01

We have summarized experimental data on the phase diagram of the system Ag 2 S–Ag 2 Se. Standard thermodynamic functions of four solid solutions in this system have been calculated using the model of regular and subregular solutions: a restricted fcc solid solution γ-Ag 2 S-Ag 2 S 1−x Se x (x 2 S–Ag 2 Se, monoclinic solid solution (α) from Ag 2 S to Ag 2 S 0.4 Se 0.6 , and orthorhombic solid solution (α) from Ag 2 S 0.3 Se 0.7 to the Ag 2 Se. G mix and S mix have been evaluated using the subregular model for asymmetric solution for the region Ag 2 S 0.4 Se 0.6 –Ag 2 S 0.3 Se 0.7 . The thermodynamic data can be used for modeling in complex natural systems and in matters of semiconductor materials

Tailoring the structural and optical properties of TiN thin films by Ag ion implantation

Energy Technology Data Exchange (ETDEWEB)

Popović, M., E-mail: majap@vinca.rs; Novaković, M.; Rakočević, Z.; Bibić, N.

2016-12-15

Highlights: • Changes in structural and optical properties of TiN films induced by Ag ions. • The formation of Ag metallic clusters inside of TiN layers was observed. • The SPR of Ag particles was confirmed by a broad band in the spectra. • As the Ag ions fluence increases the n also increase and k values decrease. • With increasing ion fluence the TiN film becomes more metallic. - Abstract: Titanium nitride (TiN) thin films thickness of ∼260 nm prepared by dc reactive sputtering were irradiated with 200 keV silver (Ag) ions to the fluences ranging from 5 × 10{sup 15} ions/cm{sup 2} to 20 × 10{sup 15} ions/cm{sup 2}. After implantation TiN layers were annealed 2 h at 700 °C in a vacuum. Ion irradiation-induced microstructural changes were examined by using Rutherford backscattering spectrometry, X-ray diffraction and transmission electron microscopy, while the surface topography was observed using atomic force microscopy. Spectroscopic ellipsometry was employed to get insights on the optical and electronic properties of TiN films with respect to their microstructure. The results showed that the irradiations lead to deformation of the lattice, increasing disorder and formation of new Ag phase. The optical results demonstrate the contribution of surface plasmon resonace (SPR) of Ag particles. SPR position shifted in the range of 354.3–476.9 nm when Ag ion fluence varied from 5 × 10{sup 15} ions/cm{sup 2} to 20 × 10{sup 15} ions/cm{sup 2}. Shift in peak wavelength shows dependence on Ag particles concentration, suggesting that interaction between Ag particles dominate the surface plasmon resonance effect. Presence of Ag as second metal in the layer leads to overall decrease of optical resistivity of TiN.

Evidence for a saturable mechanism of disappearance of standard heparin in rabbits

International Nuclear Information System (INIS)

Boneu, B.; Caranobe, C.; Gabaig, A.M.; Dupouy, D.; Sie, P.; Buchanan, M.R.; Hirsh, J.

1987-01-01

This work demonstrates that after bolus intravenous injection standard heparin (SH) disappearance results from the combination of a saturable and a non saturable mechanism. Pharmacokinetics and pharmacodynamics of SH were studied by measuring the disappearance of increasing doses (5 - 500 anti-factor Xa U/kg) of 125 I-heparin and of its biological effects. CPM curves allowed the determination of the half lives of heparin according to the dose injected. The half lives were clearly dose dependent and reached a plateau over 100 anti-factor Xa U/kg. The complex curve which describes the amount of heparin cleared per time unit after any given dose has been resolved into its two components reflecting a saturable and a non saturable mechanism of disappearance. For the doses less than 100 anti-factor Xa U/kg the saturable mechanism was preeminent and the anti-factor Xa activity disappearance followed an exponential pattern; for the doses less than 100 anti-factor Xa U/kg the contribution of the non saturable mechanism becomes more important and the anti-factor Xa activity disappearance followed a concave-convex pattern. Further experiments showed that the heparin half life shortened as the circulating anti-factor Xa activity decreased; this phenomenon may explain the concave-convex pattern of the curve of the anticoagulant effect observed after injection of large doses of SH

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

Ag/α-Fe2O3 hollow microspheres: Preparation and application for hydrogen peroxide detection

International Nuclear Information System (INIS)

Kang, Xinyuan; Wu, Zhiping; Liao, Fang; Zhang, Tingting; Guo, Tingting

2015-01-01

In this paper, we demonstrated a simple approach for preparing α-Fe 2 O 3 hollow spheres by mixing ferric nitrate aqueous and glucose in 180 °C. The glucose was found to act as a soft template in the process of α-Fe 2 O 3 hollow spheres formation. Ag/α-Fe 2 O 3 hollow nanocomposite was obtained under UV irradiation without additional reducing agents or initiators. Synthesized Ag/α-Fe 2 O 3 hollow composites exhibited remarkable catalytic performance toward H 2 O 2 reduction. The electrocatalytic activity mechanism of Ag/α-Fe 2 O 3 /GCE were discussed toward the reduction of H 2 O 2 in this paper. - Graphical abstract: Glucose is carbonized as carbon balls in the 180 °C hydrothermal carbonization process, which plays a role of a soft template. Carbon spherical shell is rich in many hydroxyls, which have good hydrophilicity and surface reactivity. When Fe(NO 3 ) 3 is added to the aqueous solution of Glucose, the hydrophilic -OH will adsorb Fe 3+ to form coordination compound by coordination bond. α-FeOOH is formed on the surface of carbon balls by hydrothermal reaction. After calcination at 500 °C, carbon spheres react with oxygen to form carbon dioxide, which disappears in the air. Meanwhile α-FeOOH is calcined to form α-Fe 2 O 3 hollow spheres.

Analysis and visualisation of lake disappearance process in Iława Lakeland Landscape Park

Directory of Open Access Journals (Sweden)

Marynowska Weronika Cecylia

2018-03-01

Full Text Available Lake disappearance as a natural stage of evolution of lakes is an extremely important issue in the landscape and ecosystem research context. Studies of the changes that occur in the lake landscape, characteristic in the northern part of Poland, are aimed at defining the cause and forecasting the results. The possibilities of the Geographic Information Systems (GIS were used in this paper to analyse and visualise the process of lake disappearance in the Iława Lakeland Landscape Park. GIS technologies which primarily are used for gathering, storing, processing and presenting spatial data have been used to interpret changes in lakes coverage over a period of 100 years. The analysis were based on data bases and cartographic former maps such as hydrographic maps, attribute data and bathymetric plans. The data was gathered by transfer from different geoportals, next vectorised, and then preprocessed. Former maps were rectified. The lake disappearance process was presented in several forms: lake cards, animations and interactive map. Basing on the GIS analysis about lake disappearance in Iława Lakeland Landscape Park it was possible to state that lakes are disappearing in rate of 3.99 ha a−1.

Synthesis of Silver nanoparticles (AgNPs) with Antibacterial Activity

Science.gov (United States)

Campillo Gloria, E.; Ederley, Vélez; Gladis, Morales; César, Hincapié; Jaime, Osorio; Oscar, Arnache; Uribe José, Ignacio; Franklin, Jaramillo

2017-06-01

The synthesis of nanomaterials is currently one of the most active in nanoscience branches; especially those help improve the human quality life. Silver nanoparticles (AgNPs) are an example of this as it is known to have inhibitory and bactericidal effects. In this work, we report the synthesis of silver nanoparticles by chemical reduction method of silver nitrate (AgNO3) from aqueous solution, using a mix of polivinyl pyrrolidone (PVP) - Aloe Vera as reducing agent and for stabilization and control of particle size. Silver nanoparticles obtained were characterized by Scanning Electron Microscopy (SEM), UV-visible spectroscopy and measurements using Zetasizer Nano ZS were applied to size estimation. The existence of surface plasmon resonance peak at λmax ~ 420 nm is evidence of silver nanoparticles formation. It was possible to standardize an appropriate protocol for the evaluation of bactericidal activity of the nanoparticles, for mesophilic microorganisms. Bactericidal activity above 90% against these kinds of bacteria was demonstrated.

Synthesis of Silver nanoparticles (AgNPs) with Antibacterial Activity

International Nuclear Information System (INIS)

Gloria, E. Campillo; Ederley, Vélez; César, Hincapié; Gladis, Morales; Jaime, Osorio; Oscar, Arnache; José, Ignacio Uribe; Franklin, Jaramillo

2017-01-01

The synthesis of nanomaterials is currently one of the most active in nanoscience branches; especially those help improve the human quality life. Silver nanoparticles (AgNPs) are an example of this as it is known to have inhibitory and bactericidal effects. In this work, we report the synthesis of silver nanoparticles by chemical reduction method of silver nitrate (AgNO 3 ) from aqueous solution, using a mix of polivinyl pyrrolidone (PVP) – Aloe Vera as reducing agent and for stabilization and control of particle size. Silver nanoparticles obtained were characterized by Scanning Electron Microscopy (SEM), UV–visible spectroscopy and measurements using Zetasizer Nano ZS were applied to size estimation. The existence of surface plasmon resonance peak at λ max ∼ 420 nm is evidence of silver nanoparticles formation. It was possible to standardize an appropriate protocol for the evaluation of bactericidal activity of the nanoparticles, for mesophilic microorganisms. Bactericidal activity above 90% against these kinds of bacteria was demonstrated. (paper)

Synthesis and visible-light photocatalytic property of Ag/GO/g-C{sub 3}N{sub 4} ternary composite

Energy Technology Data Exchange (ETDEWEB)

Zhang, Yanxiang [Rural Environmental Engineering Center of Qingdao, College of Resource and Environment, Qingdao Agricultural University, Qingdao 266109 (China); College of Environmental Science and Engineering, Shandong University, Jinan 250100 (China); State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150090 (China); Wu, Juan; Deng, Yangyang; Xin, Yanjun [Rural Environmental Engineering Center of Qingdao, College of Resource and Environment, Qingdao Agricultural University, Qingdao 266109 (China); Liu, Huiling [State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150090 (China); Ma, Dong, E-mail: madong8088@126.com [Rural Environmental Engineering Center of Qingdao, College of Resource and Environment, Qingdao Agricultural University, Qingdao 266109 (China); Bao, Nan [College of Environmental Science and Engineering, Shandong University, Jinan 250100 (China)

2017-07-15

Highlights: • The Ag/GO/g-C{sub 3}N{sub 4} composite photocatalyst was obtained. • The GO acts as the electron mediator in the composite photocatalyst. • The composite has much higher photocatalytic activity than that of pure one. • The matched Fermi level provides the favorable charge transfer in the composite. - Abstract: Ag/GO/g-C{sub 3}N{sub 4} composites were successfully synthesized by a sonochemical method. The structure and properties of the composites at various Ag loadings were characterized, and the Ag nanoparticles were confirmed by XRD, TEM and XPS measurements. UV–Vis diffuse reflectance spectra showed the presence of surface plasmon peak for Ag at 550 nm. The Ag/GO/g-C{sub 3}N{sub 4} composites demonstrated excellent activity in photocatalytic degradation of Rh B under visible light irradiation, and 5% of Ag nanoparticle was found to be the most suitable loading. The enhanced photocatalytic activity was ascribed to the role of GO nanosheets and Ag nanoparticles. The GO nanosheets acted as electrons transporter and acceptor in the composite and inhibited the charge recombination. The Ag nanoparticles acted as an electron traps to facilitate the separation of photogenerated electron-hole pairs and promoted interfacial electrons transfer. The {sup ·}OH{sub ads} and h{sup +} were the major radicals to be involved in the photocatalytic process.

Disappearance of some autonomously functioning thyroid nodules following TSH stimulation: Pathogenetic hypothesis

Energy Technology Data Exchange (ETDEWEB)

Vattimo, A.; Pisani, M.; Martini, G.

1983-04-01

The disappearance of a hot nodule following TSH stimulation has been observed in 6 subjects with autonomously functioning thyroid nodule, in the thyroid scan obtained using sup(99m)Tc-pertechnetate and /sup 131/I. These findings have been related by many workers to the hyperreactivity of the nodular tissue to TSH: the disappearance of the nodule is due to a more rapid turnover of the tracer. In this work a new pathogenetic hypothesis is proposed: the disappearance of hot thyroid nodules might be due to ischaemia induced by the reaction of the healthy tissue, which had previously been inhibited. This hypothesis is confirmed by the scans performed shortly after administration of the tracers.

Disappearance of some autonomously functioning thyroid nodules following TSH stimulation: Pathogenetic hypothesis

International Nuclear Information System (INIS)

Vattimo, A.; Pisani, M.; Martini, G.

1983-01-01

The disappearance of a hot nodule following TSH stimulation has been observed in 6 subjects with autonomously functioning thyroid nodule, in the thyroid scan obtained using sup(99m)Tc-pertechnetate and 131 I. These findings have been related by many workers to the hyperreactivity of the nodular tissue to TSH: the disappearance of the nodule is due to a more rapid turnover of the tracer. In this work a new pathogenetic hypothesis is proposed: the disappearance of hot thyroid nodules might be due to ischaemia induced by the reaction of the healthy tissue, which had previously been inhibited. This hypothesis is confirmed by the scans performed shortly after administration of the tracers. (orig.) [de

Precision Search for Muon Antineutrino Disappearance Oscillations Using a Dual Baseline Technique

Energy Technology Data Exchange (ETDEWEB)

Cheng, Gary Li [Columbia Univ., New York, NY (United States)

2013-01-01

A search for short baseline muon antineutrino disappearance with the SciBooNE and MiniBooNE experiments at Fermi National Accelerator Laboratory in Batavia, Illinois is presented. Short baseline muon antineutrino disappearance measurements help constrain sterile neutrino models. The two detectors observe muon antineutrinos from the same beam, therefore the combined analysis of their data sets serves to partially constrain some of the flux and cross section uncertainties. A likelihood ratio method was used to set a 90% confidence level upper limit on muon antineutrino disappearance that dramatically improves upon prior sterile neutrino oscillation limits in the Δm²=0.1-100 eV² region.

AGS experiments: 1993 - 1994 - 1995

Energy Technology Data Exchange (ETDEWEB)

Depken, J.C.

1996-04-01

This report contains: FY 1995 AGS Schedule as Run; FY 1996-97 AGE Schedule (working copy); AGS Beams 1995; AGS Experimental Area FY 1993 Physics Program; AGS Experimental Area FY 1994 Physics Program; AGS Experimental Area FY 1995 Physics Program; AGS Experimental Area FY 1996 Physics Program (In progress); A listing of experiments by number; Two-page summaries of each experiment begin here, also ordered by number; Listing of publications of AGS experiments begins here; and Listing of AGS experimenters begins here. This is the twelfth edition.

AGS experiments: 1993 - 1994 - 1995

International Nuclear Information System (INIS)

Depken, J.C.

1996-04-01

This report contains: FY 1995 AGS Schedule as Run; FY 1996-97 AGE Schedule (working copy); AGS Beams 1995; AGS Experimental Area FY 1993 Physics Program; AGS Experimental Area FY 1994 Physics Program; AGS Experimental Area FY 1995 Physics Program; AGS Experimental Area FY 1996 Physics Program (In progress); A listing of experiments by number; Two-page summaries of each experiment begin here, also ordered by number; Listing of publications of AGS experiments begins here; and Listing of AGS experimenters begins here. This is the twelfth edition

Frequency upconversion in Er3+ doped tungsten tellurite glass containing Ag nanoparticles

Science.gov (United States)

Mahajan, S. K.; Parashar, J.

2018-05-01

The frequency upconversion emission in Er3+ doped TeO2-WO3-Li2O containing Ag nanoparticle (TWLEOAG) glasses at 980nm excitation is reported. The absorption spectra reveal not only the peaks due to Er3+ ions, but also the surface plasmon resonance band of silver NPs located around 525nm and 650 nm. The spherical AgNPs with average size ˜38 nm in the glassy matrix is evidenced from the TEM measurement. Under 980nm laser excitation upconversion emission spectra show two major emission at 550nm and 638nm originating from 4S3/2 and 4F9/2 energy levels of the Er3+ ions, respectively was observed. Upconversion emission enhancement factor 7 fold has been measured for sample heat treated during 40h. However for 18h heat treated TWLEOAG sample under 980 nm flash lamp excitation produced Intense green compare to red emission. Since the 980nm frequency is far from the AgNPs surface plasmon resonance frequency, visible emission ehancement is attributed to local field increase in proximity of the Ag NPs and not energy tranfer from NPs to emitters. Possible energy transfer upconversion mechanism has been also discussed.

Sonochemical synthesis of Ag/AgCl nanocubes and their efficient visible-light-driven photocatalytic performance.

Science.gov (United States)

Chen, Deliang; Yoo, Seung Hwa; Huang, Qingsong; Ali, Ghafar; Cho, Sung Oh

2012-04-23

A novel one-step sonochemical approach to synthesize a plasmonic photocatalyst of AgCl nanocubes (ca. 115 nm in edge length) with a small amount of Ag metal species is presented. The nanoscale Ag/AgCl hybrid photocatalysts with cubic morphology are readily formed under ambient ultrasonic conditions and neither external heat treatment nor reducing agents are required. The size of the Ag/AgCl photocatalysts could be controlled by changing the concentrations of Ag(+) ions and polyvinylpyrrolidone molecules in precursor solutions. The compositions, microstructures, influencing factors, and possible growth mechanism of the Ag/AgCl hybrid nanocubes were systematically investigated. The Ag/AgCl photocatalysts show excellent photocatalytic performance for degradation of various dye molecules under visible light. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Thin silica shell coated Ag assembled nanostructures for expanding generality of SERS analytes.

Directory of Open Access Journals (Sweden)

Myeong Geun Cha

Full Text Available Surface-enhanced Raman scattering (SERS provides a unique non-destructive spectroscopic fingerprint for chemical detection. However, intrinsic differences in affinity of analyte molecules to metal surface hinder SERS as a universal quantitative detection tool for various analyte molecules simultaneously. This must be overcome while keeping close proximity of analyte molecules to the metal surface. Moreover, assembled metal nanoparticles (NPs structures might be beneficial for sensitive and reliable detection of chemicals than single NP structures. For this purpose, here we introduce thin silica-coated and assembled Ag NPs (SiO2@Ag@SiO2 NPs for simultaneous and quantitative detection of chemicals that have different intrinsic affinities to silver metal. These SiO2@Ag@SiO2 NPs could detect each SERS peak of aniline or 4-aminothiophenol (4-ATP from the mixture with limits of detection (LOD of 93 ppm and 54 ppb, respectively. E-field distribution based on interparticle distance was simulated using discrete dipole approximation (DDA calculation to gain insight into enhanced scattering of these thin silica coated Ag NP assemblies. These NPs were successfully applied to detect aniline in river water and tap water. Results suggest that SiO2@Ag@SiO2 NP-based SERS detection systems can be used as a simple and universal detection tool for environment pollutants and food safety.

Long baseline neutrino oscillation experiment at the AGS. Physics design report

Energy Technology Data Exchange (ETDEWEB)

Beavis, D.; Carroll, A.; Chiang, I. [Brookhaven National Lab., Long Island, NY (United States); E889 Collaboration

1995-04-01

The authors present a design for a multi-detector long baseline neutrino oscillation experiment at the BNL AGS. It has been approved by the BNL-HENP-PAC as AGS Experiment 889. The experiment will search for oscillations in the {nu}{sub {mu}}, disappearance channel and the {nu}{sub {mu}} {leftrightarrow} {nu}{sub e} appearance channel by means of four identical neutrino detectors located 1, 3, 24, and 68km from the AGS neutrino source. Observed depletion of the {nu}{sub {mu}} flux (via quasi-elastic muon neutrino events, {nu}{sub {mu}}n {yields} {mu}{sup {minus}}p) in the far detectors not attended by an observed proportional increase of the {nu}{sub e} flux (via quasi-elastic electron neutrino events, {nu}{sub e}n {yields} e{sup {minus}}p) in those detectors will be prima facie evidence for the oscillation channel {nu}{sub {mu}} {leftrightarrow} {nu}{sub {tau}}. The experiment is directed toward exploration of the region of the neutrino oscillation parameters {Delta}m{sup 2} and sin{sup 2}2{theta}, suggested by the Kamiokande and IMB deep underground detectors but it will also explore a region more than two orders of magnitude larger than that of previous accelerator experiments. The experiment will run in a mode new to BNL. It will receive the fast extracted proton beam on the neutrino target approximately 20 hours per day when the AGS is not filling RHIC. A key aspect of the experimental design involves placing the detectors 1.5 degrees off the center line of the neutrino beam, which has the important advantage that the central value of the neutrino energy ({approx} 1 GeV) and the beam spectral shape are, to a good approximation, the same in all four detectors. The proposed detectors are massive, imaging, water Cherenkov detectors similar in large part to the Kamiokande and IMB detectors. The design has profited from their decade-long experience, and from the detector designs of the forthcoming SNO and SuperKamiokande detectors.

Long baseline neutrino oscillation experiment at the AGS. Physics design report

International Nuclear Information System (INIS)

Beavis, D.; Carroll, A.; Chiang, I.

1995-04-01

The authors present a design for a multi-detector long baseline neutrino oscillation experiment at the BNL AGS. It has been approved by the BNL-HENP-PAC as AGS Experiment 889. The experiment will search for oscillations in the ν μ , disappearance channel and the ν μ ↔ ν e appearance channel by means of four identical neutrino detectors located 1, 3, 24, and 68km from the AGS neutrino source. Observed depletion of the ν μ flux (via quasi-elastic muon neutrino events, ν μ n → μ - p) in the far detectors not attended by an observed proportional increase of the ν e flux (via quasi-elastic electron neutrino events, ν e n → e - p) in those detectors will be prima facie evidence for the oscillation channel ν μ ↔ ν τ . The experiment is directed toward exploration of the region of the neutrino oscillation parameters Δm 2 and sin 2 2θ, suggested by the Kamiokande and IMB deep underground detectors but it will also explore a region more than two orders of magnitude larger than that of previous accelerator experiments. The experiment will run in a mode new to BNL. It will receive the fast extracted proton beam on the neutrino target approximately 20 hours per day when the AGS is not filling RHIC. A key aspect of the experimental design involves placing the detectors 1.5 degrees off the center line of the neutrino beam, which has the important advantage that the central value of the neutrino energy (∼ 1 GeV) and the beam spectral shape are, to a good approximation, the same in all four detectors. The proposed detectors are massive, imaging, water Cherenkov detectors similar in large part to the Kamiokande and IMB detectors. The design has profited from their decade-long experience, and from the detector designs of the forthcoming SNO and SuperKamiokande detectors

Optical properties of silicene, Si/Ag(111), and Si/Ag(110)

Science.gov (United States)

Hogan, C.; Pulci, O.; Gori, P.; Bechstedt, F.; Martin, D. S.; Barritt, E. E.; Curcella, A.; Prevot, G.; Borensztein, Y.

2018-05-01

We present a state-of-the-art study of the optical properties of free-standing silicene and of single-layer Si one- and two-dimensional (1D and 2D) nanostructures supported on Ag(110) and Ag(111) substrates. Ab initio simulations of reflectance anisotropy spectroscopy (RAS) and surface differential reflectivity spectroscopy (SDRS) applied to the clean Ag surface and Si/Ag interfaces are compared with new measurements. For Si/Ag(110), we confirm a pentagonal nanoribbon geometry, strongly bonded to the substrate, and rule out competing zigzag chain and silicenelike models. For Si/Ag(111), we reproduce the main experimental features and isolate the optical signal of the epitaxial silicene overlayer. The absorption spectrum of a silicene sheet computed including excitonic and local field effects is found to be quite similar to that calculated within an independent particle approximation and shows strong modifications when adsorbed on a Ag substrate. Important details of the computational approach are examined and the origins of the RAS and SDRS signals are explained in terms of the interface and substrate response functions. Our study does not find any evidence for Si adlayers that retain the properties of freestanding silicene.

Synthesis and characterizations of AgSCN nanospheres using AgCl as the precursor

International Nuclear Information System (INIS)

Yang Ming; Ma Jing

2009-01-01

Nanospheres of AgSCN with an average radius of 30-80 nm have been prepared by a simple reaction between AgCl suspension and KSCN in the presence of gelatin. Gelatin played a decisive role as an inhibitor of the direct attack of SCN - ions to AgCl surfaces and coagulation of the growing AgSCN in producing the spherical AgSCN nanoparticles. The products were characterized by X-ray powder diffraction, transmission electron microscopy and X-ray photoelectron spectra techniques. The electrical conductivity of thin films of as-prepared AgSCN nanoparticles and polyethylene oxide (PEO) at room temperature was measured. The maximum value of electrical conductivity of as-prepared AgSCN-PEO was 1.53 x 10 -5 S cm -1 .

Sensitive and selective detection of Hg2+ and Cu2+ ions by fluorescent Ag nanoclusters synthesized via a hydrothermal method

Science.gov (United States)

Liu, Jing; Ren, Xiangling; Meng, Xianwei; Fang, Zheng; Tang, Fangqiong

2013-09-01

An easily prepared fluorescent Ag nanoclusters (Ag NCs) probe for the sensitive and selective detection of Hg2+ and Cu2+ ions was developed here. The Ag NCs were synthesized by using polymethacrylic acid sodium salt as a template via a convenient hydrothermal process. The as-prepared fluorescent Ag NCs were monodispersed, uniform and less than 2 nm in diameter, and can be quenched in the presence of mercury (Hg2+) or copper (Cu2+) ions. Excellent linear relationships existed between the quenching degree of the Ag NCs and the concentrations of Hg2+ or Cu2+ ions in the range of 10 nM to 20 μM or 10 nM to 30 μM, respectively. By using ethylenediaminetetraacetate (EDTA) as the masking agent of Cu2+, Hg2+ was exclusively detected in coexistence with Cu2+ with high sensitivity (LOD = 10 nM), which also provided a reusable detection method for Cu2+. Furthermore, the different quenching phenomena caused by the two metals ions such as changes in visible colour, shifts of UV absorbance peaks and changes in size of Ag NCs make it easy to distinguish between them. Therefore the easily synthesized fluorescent Ag NCs may have great potential as Hg2+ and Cu2+ ions sensors.An easily prepared fluorescent Ag nanoclusters (Ag NCs) probe for the sensitive and selective detection of Hg2+ and Cu2+ ions was developed here. The Ag NCs were synthesized by using polymethacrylic acid sodium salt as a template via a convenient hydrothermal process. The as-prepared fluorescent Ag NCs were monodispersed, uniform and less than 2 nm in diameter, and can be quenched in the presence of mercury (Hg2+) or copper (Cu2+) ions. Excellent linear relationships existed between the quenching degree of the Ag NCs and the concentrations of Hg2+ or Cu2+ ions in the range of 10 nM to 20 μM or 10 nM to 30 μM, respectively. By using ethylenediaminetetraacetate (EDTA) as the masking agent of Cu2+, Hg2+ was exclusively detected in coexistence with Cu2+ with high sensitivity (LOD = 10 nM), which also provided a

Thermal expansion properties of Bi-2212 in Ag or an Ag-alloy matrix

International Nuclear Information System (INIS)

Tenbrink, J.; Krauth, H.

1994-01-01

The thermal expansion properties of polycrystalline Bi 2 Sr 2 Ca 1 Cu 2 O 8+x melt-processed bulk specimens, and Bi 2 Sr 2 Ca 1 Cu 2 O 8+x monocore as well as multifilamentary round wires in Ag or Ag-alloy matrix have been investigated over the temperature range from -150 to 800 degrees C. Although the thermal expansion of Bi 2 Sr 2 Ca 1 Cu 2 O 8+x is distinctly lower compared with Ag, the thermal expansion properties of the Bi 2 Sr 2 Ca 1 Cu 2 O 8+x -Ag or AgNiMg-alloy composite conductors are essentially governed by the matrix material. The thermal expansion of the encountered oxide-dispersion-strengthened AgNiMg alloys is only slightly lower compared with that of pure Ag. Therefore the thermal expansion of all investigated Bi 2 Sr 2 Ca 1 Cu 2 O 8+x -Ag or Ag-alloy composite wires was found to be close to that of pure Ag. The reason for this striking behaviour is shown to be related to a surprisingly low elastic modulus of the polycrystalline Bi-2212 wire cores of the order of 10 to a maximum 40 GPa. (author)

Dosimetric characteristics of Li2B4O7:Cu,Ag,P solid TL detectors

International Nuclear Information System (INIS)

Proki, M.

2002-01-01

The main dosimetric characteristics are presented of newly prepared tissue-equivalent, highly sensitive thermoluminescent detector, Li 2 B 4 O 7 :Cu,Ag,P in the form of sintered pellets, developed at the Institute of Nuclear Sciences, Vin a . As a result of an advancement in the preparation procedure by the sensitising of basic copper activated lithium borate TL material, significant improvement in the TL sensitivity of Li 2 B 4 O 7 :Cu,Ag,P was gained. The glow curve of Li 2 B 4 O 7 :Cu,Ag,P consists of well defined main dosimetric peak situated at about 185-190 deg. C with the TL sensitivity which is about four to five times higher than that of LiF:Mg,Ti (TLD-100). From the experimental results a very wide linear dose response range, up to 10 3 Gy is evident. Dosimetric characteristics make sintered solid Li 2 B 4 O 7 :Cu,Ag,P TL detectors very promising for different dosimetry applications particularly in medical dosimetry and also for individual monitoring. (author)

Material for 258 atom bombs disappeared?

International Nuclear Information System (INIS)

Gruemm, H.

1988-01-01

In a report published in the news magazine, 'Der Spiegel', it was said that IAEA safeguards obviously had failed, for large amounts of fissile material had disappeared, which could be turned into 258 atomic bombs. The article in this issue of atw by the former Deputy Director General with the IAEA Safeguards Division sketches the background to the assertions made by 'Der Spiegel' and presents an overview of the inspection and verification methods employed by IAEA. (orig./HP) [de

Facile synthesis of silver/silver thiocyanate (Ag@AgSCN plasmonic nanostructures with enhanced photocatalytic performance

Directory of Open Access Journals (Sweden)

Xinfu Zhao

2017-12-01

Full Text Available A nanostructured plasmonic photocatalyst, silver/silver thiocyanate (Ag@AgSCN, has been prepared by a simple precipitation method followed by UV-light-induced reduction. The ratio of Ag to silver thiocyanate (AgSCN can be controlled by simply adjusting the photo-induced reduction time. The formation mechanism of the product was investigated based on the time-dependent experiments. Further experiments indicated that the prepared Ag@AgSCN nanostructures with an atomic ratio of Ag/AgSCN = 0.0463 exhibited high photocatalytic activity and long-term stability for the degradation of oxytetracycline (84% under visible-light irradiation. In addition to the microstructure and high specific surface area, the enhanced photocatalytic activity was mainly caused by the surface plasmon resonance of Ag nanoparticles, and the high stability of AgSCN resulted in the long-term stability of the photocatalyst product.

Sensitive electrochemical sensor of tryptophan based on Ag-C core-shell nanocomposite modified glassy carbon electrode

Energy Technology Data Exchange (ETDEWEB)

Mao Shuxian [College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123 (China); Li Weifeng, E-mail: liweifeng@suda.edu.cn [College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123 (China); Long Yumei, E-mail: yumeilong@suda.edu.cn [College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123 (China); Tu Yifeng; Deng, Anping [College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123 (China)

2012-08-13

Graphical abstract: Ag-C and Colloidal carbon sphere modified glassy carbon electrodes were prepared. It was clear that the Ag-C/GCE exhibited enhanced electrocatalytic activity towards Trp, which could result from the synergistic effect between Ag core and carbon shell. The Ag-C/GCE showed excellent analytical properties in the determination of Trp. Highlights: Black-Right-Pointing-Pointer The electrochemical behavior of Ag-C core-shell nanocomposite was firstly proposed. Black-Right-Pointing-Pointer Ag-C/GC electrode exhibited favorable electrocatalytic properties towards Trp. Black-Right-Pointing-Pointer The good electrocatalysis was due to the synergistic effect of Ag-core and C-shell. Black-Right-Pointing-Pointer The Ag-C/GC electrode displayed excellent analytical properties in determining Trp. - Abstract: We here reported a simple electrochemical method for the detection of tryptophan (Trp) based on the Ag-C modified glassy carbon (Ag-C/GC) electrode. The Ag-C core-shell structured nanoparticles were synthesized using one-pot hydrothermal method and characterized by scanning electron microscope (SEM), transmission electron microscope (TEM), and Fourier transform-infrared spectroscopy (FTIR). The electrochemical behaviors of Trp on Ag-C/GC electrode were investigated and exhibited a direct electrochemical process. The favorable electrochemical properties of Ag-C/GC electrode were attributed to the synergistic effect of the Ag core and carbon shell. The carbon shell cannot only protect Ag core but also contribute to the enhanced substrate accessibility and Trp-substrate interactions, while nano-Ag core can display good electrocatalytic activity to Trp at the same time. Under the optimum experimental conditions the oxidation peak current was linearly dependent on the Trp concentration in the range of 1.0 Multiplication-Sign 10{sup -7} to 1.0 Multiplication-Sign 10{sup -4} M with a detection limit of 4.0 Multiplication-Sign 10{sup -8} M (S/N = 3). In addition

On the association of magnetic clouds with disappearing filaments

International Nuclear Information System (INIS)

Wilson, R.M.; Hildner, E.

1986-01-01

We present evidence that an interplanetary magnetic cloud preceding an interaction region, observed at earth January 24, 1974, is associated with the eruptive filament or disparition brusque (DB) near central meridian on January 18. The DB also was associated with a long-decay soft X ray transient (LDE) and a long-duration gradual-rise-and-fall (GRF) radio burst. To assess whether magnetic clouds are generally associated with DBs, we present results from statistical testing of the relation of 33 magnetic clouds (and 33 control samples without magnetic clouds) to disappearing filaments near central meridian (approx. 99% confidence. There is a suggestion that clouds following shocks, probably launched at times of solar flares, are not as strongly associated with disappearing filaments as are clouds launched less violently

Photocatalytic oxidation removal of Hg{sup 0} using ternary Ag/AgI-Ag{sub 2}CO{sub 3} hybrids in wet scrubbing process under fluorescent light

Energy Technology Data Exchange (ETDEWEB)

Zhang, Anchao, E-mail: aczhang@qq.com [School of Mechanical and Power Engineering, Henan Polytechnic University, Jiaozuo, 454000 (China); Zhang, Lixiang; Chen, Xiaozhuan; Zhu, Qifeng; Liu, Zhichao [School of Mechanical and Power Engineering, Henan Polytechnic University, Jiaozuo, 454000 (China); Xiang, Jun, E-mail: xiangjun@mail.hust.edu.cn [State Key Laboratory of Coal Combustion, Huazhong University of Science and Technology, Wuhan, 430074 (China)

2017-01-15

Highlights: • Ag/AgI-Ag{sub 2}CO{sub 3} hybrids were employed for Hg{sup 0} removal under fluorescent light. • Superoxide radical (·O{sub 2}{sup −}) played a key role in Hg{sup 0} removal. • NO exhibited a significant effect on Hg{sup 0} removal in comparison to SO{sub 2}. • The mechanism for enhanced Hg{sup 0} removal over Ag/AgI-Ag{sub 2}CO{sub 3} was proposed. - Abstract: A series of ternary Ag/AgI-Ag{sub 2}CO{sub 3} photocatalysts synthesized using a facile coprecipitation method were employed to investigate their performances of Hg{sup 0} removal in a wet scrubbing reactor. The hybrids were characterized by N{sub 2} adsorption-desorption, XRD, SEM-EDS, HRTEM, XPS, DRS and ESR. The photocatalytic activities of Hg{sup 0} removal were evaluated under fluorescent light. The results showed that AgI content, fluorescent light irradiation, reaction temperature all showed significant influences on Hg{sup 0} removal. NO exhibited significant effect on Hg{sup 0} removal in comparison to SO{sub 2}. Among these ternary Ag/AgI-Ag{sub 2}CO{sub 3} hybrids, Ag/AgI(0.1)-Ag{sub 2}CO{sub 3} showed the highest Hg{sup 0} removal efficiency, which could be ascribed to the effective separation of photogenerated electron-hole pairs between AgI and Ag{sub 2}CO{sub 3} and the surface plasmon resonance (SPR) effect in the visible region by metallic silver nanoparticles (Ag{sup 0} NPs). The trapping studies of reactive radicals showed that the superoxide radicals (·O{sub 2}{sup −}) may play a key role in Hg{sup 0} removal under fluorescent light. According to the experimental and characterization results, a possible photocatalytic oxidation mechanism for enhanced Hg{sup 0} removal over Ag/AgI(0.1)-Ag{sub 2}CO{sub 3} hybrid under fluorescent light was proposed.

Medium-range correlation of Ag ions in superionic melts of Ag{sub 2}Se and AgI by reverse Monte Carlo structural modelling-connectivity and void distribution

Energy Technology Data Exchange (ETDEWEB)

Tahara, Shuta; Ohno, Satoru [Faculty of Pharmacy, Niigata University of Pharmacy and Applied Life Sciences, 265-1 Higashijima, Akiha-ku, Niigata 956-8603 (Japan); Ueno, Hiroki; Takeda, Shin' ichi [Department of Physics, Faculty of Sciences, Kyushu University 6-10-1 Hakozaki, Higashi-ku, Fukuoka 812-8581 (Japan); Ohara, Koji; Kohara, Shinji [Research and Utilization Division, Japan Synchrotron Radiation Research Institute (JASRI, SPring-8), 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5198 (Japan); Kawakita, Yukinobu [J-PARC Center, Japan Atomic Energy Agency, 2-4 Shirakata Shirane, Tokai-mura, Naka-gun, Ibaraki 319-1195 (Japan)

2011-06-15

High-energy x-ray diffraction measurements on molten Ag{sub 2}Se were performed. Partial structure factors and radial distribution functions were deduced by reverse Monte Carlo (RMC) structural modelling on the basis of our new x-ray and earlier published neutron diffraction data. These partial functions were compared with those of molten AgI. Both AgI and Ag{sub 2}Se have a superionic solid phase prior to melting. New RMC structural modelling for molten AgI was performed to revise our previous model with a bond-angle restriction to reduce the number of unphysical Ag triangles. The refined model of molten AgI revealed that isolated unbranched chains formed by Ag ions are the cause of the medium-range order of Ag. In contrast with molten AgI, molten Ag{sub 2}Se has 'cage-like' structures with approximately seven Ag ions surrounding a Se ion. Connectivity analysis revealed that most of the Ag ions in molten Ag{sub 2}Se are located within 2.9 A of each other and only small voids are found, which is in contrast to the wide distribution of Ag-void radii in molten AgI. It is conjectured that the collective motion of Ag ions through small voids is required to realize the well-known fast diffusion of Ag ions in molten Ag{sub 2}Se, which is comparable to that in molten AgI.

Experimental and theoretical investigation on photocatalytic activities of 1D Ag/Ag2WO4 nanostructures

Science.gov (United States)

Liu, Danqing; Huang, Weicheng; Li, Long; Liu, Lu; Sun, Xiaojun; Liu, Bo; Yang, Bin; Guo, Chongshen

2017-09-01

Ag2WO4 is a significant photocatalyst that responds to UV light irradiation only, which greatly hinders it for further practical application for solar light. To address this problem, herein, 1D plasmonic Ag/Ag2WO4 photocatalysts have been fabricated by a successive process including hydrothermal synthesis to obtain Ag2WO4 followed by an additional in situ chemical-reduction process for Ag decoration. Then, the structural features, optical properties, and electronic structures of Ag2WO4 and Ag/Ag2WO4 nanowires were systematically investigated via a combination of theoretical calculations and experimental evidence. The plasmon-enhanced Ag/Ag2WO4 nanowires exhibited higher visible-light-driven photocatalytic activity, which performed a desired photodestruction ratio of 91.2% on methylene blue within 60 min and good stability in five cycles. The Ag decoration greatly facilitates visible-light harvesting and thus promotes photogenerated radical oxidation to dye, which is evidenced by the higher hydroxyl radical level of Ag/Ag2WO4 detected in the ESR test during the photocatalytic process. The theoretical calculation based on density functional theory indicates that Ag nanoparticles formed on the surface of Ag2WO4 could narrow the band gap of Ag2WO4. In addition, the surface plasmon resonance absorption effect and fast charge transfer effect in the metal-semiconductor system contribute to the photocatalytic performance of Ag/Ag2WO4.

No association between gender inequality and peak HIV prevalence in developing countries - an ecological study.

Science.gov (United States)

Kenyon, Chris R; Buyze, Jozefien

2015-01-01

The prevalence of both gender inequality and HIV prevalence vary considerably both within all developing countries and within those in sub-Saharan Africa. We test the hypothesis that the extent of gender inequality is associated with national peak HIV prevalence. Linear regression was used to test the association between national peak HIV prevalence and three markers of gender equality - the gender-related development index (GDI), the gender empowerment measure (GEM), and the gender inequality index (GII). No evidence was found of a positive relationship between gender inequality and HIV prevalence, either in the analyses of all developing countries or those limited to Africa. In the bivariate analyses limited to Africa, there was a positive association between the two measures of gender "equality" and peak HIV prevalence (GDI: coefficient 28, 95% confidence interval (CI) 9.1-46.8; GEM: coefficient 54.8, 95% CI 20.5-89.1). There was also a negative association between the marker of gender "inequality" and peak HIV prevalence (GII: coefficient -66.9, 95% CI -112.8 to -21.0). These associations all disappeared on multivariate analyses. We could not find any evidence to support the hypothesis that variations in the extent of gender inequality explain variations in HIV prevalence in developing countries.

Photoinduced formation of Ag nanoparticles on the surface of As2S3/Ag thin bilayer

International Nuclear Information System (INIS)

Binu, S; Khan, Pritam; Barik, A R; Sharma, Rituraj; Adarsh, K V; Golovchak, R; Jain, H

2014-01-01

In this article, we demonstrate the combined effect of photodoping and photoinduced-surface deposition in a bilayer of chalcogenide glass (ChG) and Ag as an alternative method to optically synthesize Ag nanoparticles (AgNP) on the surface of ChG. In our experiment, AgNP formation occurs through two distinct stages: In the first stage, Ag is transported through the As 2 S 3 layer as Ag + ions, and in the second stage Ag + ions are photo-deposited as AgNP. The ex situ x-ray photoelectron spectroscopy measurements and AFM observations show photoinduced Ag mass transport and the formation of AgNP. (paper)

Glass formation in AgI:Ag2O:V2O5 and AgI:Ag2O:(V2O5+B2O3) systems

International Nuclear Information System (INIS)

Kaushik, R.; Hariharan, K.

1988-01-01

Transport properties of glasses in the system AgI:Ag 2 O: V 2 O 5 and AgI:Ag 2 O: (V 2 O 5 +B 2 O 3 ) have ben investigated. It was found that, at high AgI concentrations, the addition of another glass former (B 2 O 3 ) did not improve the conduction characteristics of the pure vanadate glasses, the best conducting composition of which had ambient temperature, ionic conductivity comparable to that of conventional liquid electrolytes. The highest conducting composition was used as an electrolyte in the study of silver solid state cells. The discharge characteristics of different cells fabricated with the glassy electrolyte, have been compared with those having the best conducting polycrystalline ompositions as electrolytes. 11 refs.; 4 figs.; 1 table

Ag supported on carbon fiber cloth as the catalyst for hydrazine oxidation in alkaline medium

International Nuclear Information System (INIS)

Liu, Ran; Ye, Ke; Gao, Yinyi; Zhang, Wenping; Wang, Guiling; Cao, Dianxue

2015-01-01

Highlights: • CFC supported microspherical Ag is obtained by square-wave potential method. • Ag/CFC electrode has high catalytic activity toward hydrazine oxidation. • Hydrazine oxidation on the electrode proceeds by a near 4-electron pathway. - Abstract: Silver particles with microspheric structure are directly electrodeposited on carbon fiber cloth (CFC) substrate by square-wave potential electrodeposition method. The electrocatalytic behaviors of the Ag/CFC electrode toward hydrazine oxidation in alkaline solution are examined by cyclic voltammetry and chronoamperometry. An onset oxidation potential of -0.5 V and a peak current density of 30 mA cm −2 are achieved in the solution containing 1.0 mol L −1 KOH and 20.0 mmol L −1 hydrazine. The microspheric structure of the Ag/CFC electrode provides large electroactive surface area, hence, abundant active sites are vacant for hydrazine oxidation. The calculated apparent activation energies at different potentials show that hydrazine electro-oxidation at higher potential has faster kinetics than that at lower potential. In addition, the transfer electron number of hydrazine oxidation reaction on the Ag/CFC electrode is close to four, suggesting hydrazine is almost completely electrooxidized on the electrode and the full use of hydrazine fuel is basically achieved.

Optical absorption properties of Ag/SiO sub 2 composite films induced by gamma irradiation

CERN Document Server

Pan, A L; Yang, Z P; Liu, F X; Ding, Z J; Qian, Y T

2003-01-01

Mesoporous SiO sub 2 composite films with small Ag particles or clusters dispersed in them were prepared by a new method: first the matrix SiO sub 2 films were prepared by the sol-gel process combined with the dip-coating technique; then they were soaked in AgNO sub 3 solutions; this was followed by irradiation with gamma-rays at room temperature and ambient pressure. The structure of these films was examined by high-resolution transmission electron microscopy, and their optical absorption spectra were examined. It has been shown that the Ag particles grown within the porous SiO sub 2 films are very small and are highly dispersed. On increasing the soaking concentration and subjecting the samples to an additional annealing, a different peak-shift effect for the surface plasmon resonance was observed in the optical absorption measurement. Possible mechanisms of this behaviour are discussed in this paper.

Synthesis and disappearance of cholesterol and bile acids in miniature swine

International Nuclear Information System (INIS)

Dupont, J.; Butterfield, A.B.; Clow, D.J.; Lumb, W.V.; McClellan, M.A.; O'Deen, L.; Oh, S-Y.

1986-01-01

Minerature swine were fitted with indwelling cannulae at two sites in the gut and catheters in the aorta, portal vein and posterior vena cava. Radioactive acetate, alanine and glucose were administered via the duodenal cannula or the portal vein catheter and synthesis of cholesterol by gut or liver monitored via the aortic serum cholesterol specific activity. Ring labeled cholesterol was administered via jejunum and portal vein and various parameters of disappearance measured during 17 to 66 days. Conversion of cholesterol to bile acids and their subsequent disappearance from gut lumen were measured. Differences were observed in substrate preference of gut and liver and in fate of newly synthesized cholesterol. Cholesterol disappearance was found to follow a two component exponential in serum and a three component exponential in gut. Serum curves were similar to those reported for humans. Two hepatic pools of cholesterol, one accessible to lipoprotein synthesis (anabolic) and another accessible to enterohepatic circulation and 7-α-hydroxylase, were inducated

AGS experiments -- 1995, 1996 and 1997

Energy Technology Data Exchange (ETDEWEB)

Depken, J.C.; Presti, P.L.

1997-12-01

This report contains (1) FY 1995 AGS schedule as run; (2) FY 1996 AGS schedule as run; (3) FY 1997 AGS schedule as run; (4) FY 1998--1999 AGS schedule (proposed); (5) AGS beams 1997; (6) AGS experimental area FY 1995 physics program; (7) AGS experimental area FY 1996 physics program; (8) AGS experimental area FY 1997 physics program; (9) AGS experimental area FY 1998--1999 physics program (proposed); (10) a listing of experiments by number; (11) two-page summaries of each experiment, in order by number; and (12) listing of publications of AGS experiments.

AGS experiments - 1995, 1996 and 1997

International Nuclear Information System (INIS)

Depken, J.C.; Presti, P.L.

1997-12-01

This report contains (1) FY 1995 AGS schedule as run; (2) FY 1996 AGS schedule as run; (3) FY 1997 AGS schedule as run; (4) FY 1998--1999 AGS schedule (proposed); (5) AGS beams 1997; (6) AGS experimental area FY 1995 physics program; (7) AGS experimental area FY 1996 physics program; (8) AGS experimental area FY 1997 physics program; (9) AGS experimental area FY 1998--1999 physics program (proposed); (10) a listing of experiments by number; (11) two-page summaries of each experiment, in order by number; and (12) listing of publications of AGS experiments

The relation between crossover of the intergrain loss-peak temperature-field characteristics of the Ag-Bi[sub 2]Sr[sub 2]CaCu[sub 2]O[sub x] screen-printed tapes and their J[sub C] values

Energy Technology Data Exchange (ETDEWEB)

Noji, H [IRC in Superconductivity, Univ. of Cambridge (United Kingdom); Glowacki, B A [IRC in Superconductivity, Univ. of Cambridge (United Kingdom) Dept. of Materials Science and Metallurgy, Univ. of Cambridge (United Kingdom); Oota, A [Dept. of Electric and Electronic Engineering, Toyohashi Univ. of Tech., (Japan)

1993-05-10

A study of the influence of the processing conditions of Ag-Bi[sub 2]Sr[sub 2]CaCu[sub 2]O[sub x] screen-printed tapes on the temperature, field and frequency dependence of their a.c. susceptibility has been conducted. Samples have been prepared by melt-solidification and subsequent sintering on silver substrates under the same conditions but with different cooling procedures and reannealing. These procedures lead to different Tc values and field dependency of the loss peak temperature T[sub M], which cause the crossover in the T[sub M] versus applied field characteristics. It was established that the above crossover phenomenon is correlated to the crossover in the J[sub C] versus temperature characteristics. (orig.)

Ag induced electromagnetic interference shielding of Ag-graphite/PVDF flexible nanocomposites thinfilms

Science.gov (United States)

Kumaran, R.; Alagar, M.; Dinesh Kumar, S.; Subramanian, V.; Dinakaran, K.

2015-09-01

We report Ag nanoparticle induced Electromagnetic Interference (EMI) shielding in a flexible composite films of Ag nanoparticles incorporated graphite/poly-vinylidene difluoride (PVDF). PVDF nanocomposite thin-films were synthesized by intercalating Ag in Graphite (GIC) followed by dispersing GIC in PVDF. The X-ray diffraction analysis and the high-resolution transmission electron microscope clearly dictate the microstructure of silver nanoparticles in graphite intercalated composite of PVDF matrix. The conductivity values of nanocomposites are increased upto 2.5 times when compared to neat PVDF having a value of 2.70 S/cm at 1 MHz. The presence of Ag broadly enhanced the dielectric constant and lowers the dielectric loss of PVDF matrix proportional to Ag content. The EMI shielding effectiveness of the composites is 29.1 dB at 12.4 GHz for the sample having 5 wt. % Ag and 10 wt. % graphite in PVDF.

Stability of nanosized alloy thin films: Faulting and phase separation in metastable Ni/Cu/Ag-W films

International Nuclear Information System (INIS)

Csiszár, G.; Kurz, S.J.B.; Mittemeijer, E.J.

2016-01-01

A comparative study of Me(=Ni/Cu/Ag)-based, W-alloyed, nanocrystalline, heavily faulted thin films was carried out to identify parameters stabilizing the nanocrystalline nature upon thermal treatment. The three systems, initially of comparably, heavily twinned (twin boundaries at spacings of 1–5 nm) microstructures showed similarities but also strikingly different behaviours upon annealing, as observed by application of in particular X-ray diffraction (line-broadening) analysis and (high resolution) transmission electron microscopy. During annealing in the range of 30–600 °C, (i) segregation at the planar faults (for Me = Ni) and at grain boundaries (for Me = Ni,Cu,Ag), as well as nanoscale phase separation (for Me = Cu,Ag) take place, (ii) distinct grain growth does not occur and (iii) the twin boundaries either are largely preserved ((Ni(W) and Ag(W)) or disappear totally (Cu(W))), which was ascribed to an altered faulting energy, due to change of the amount of W segregated at the twin boundaries, and to the evolution of nano-precipitates. The nanosized films exhibit very large internal (macro)stresses parallel to the surface, which change during annealing in the range of 1 GPa (tensile) to −3 GPa (compressive) and thus are sensitive to the microstructural changes in the films (decomposition and relaxation) that happen on a nanoscale. The results are discussed in terms of thermodynamic and/or kinetic constraints controlling these processes and thus the thermal stability of the systems concerned.

Electronic and optical properties of AgAlO_2: A first-principles study

International Nuclear Information System (INIS)

Bhamu, K.C.; Priolkar, K.R.

2017-01-01

In this paper, we present electronic and optical properties of silver-based delafossite compound AgAlO_2 (AAO). For the electronic properties, we have computed band structure and density of states. The origin of band structure is elucidated in terms of density of states. A significant contribution in band structure comes from Ag-4d and O-2p states around the Fermi level. The estimated band gap shows the indirect semiconducting nature of AAO having the band gap value of 2.34 eV. For the optical properties, we have calculated frequency dependent dielectric functions. The peaks in the imaginary component of dielectric function are explained by electronic transitions in the dispersion relation. Our computed results are in agreement with those available in the literature. The wide band gap and hence transparency for the UV and visible incident light photons makes AAO a precious material for transparent electronics. - Highlights: • Applied different-different types of exchange-correlations and potentials. • Becke–Johnson with Hubbard potential (BJ + U) is better for 2H-AgAlO_2. • Band gap is in reasonable agreement with experimentally reported. • Origin of energy bands is elucidated in terms of density of states. • 2H-AgAlO_2 is a promising candidate for transparent electronics.

Synthesis, characterization and optical properties of gelatin doped with silver nanoparticles

Science.gov (United States)

Mahmoud, K. H.; Abbo, M.

2013-12-01

In this study, silver nanoparticles were synthesized by chemical reduction of silver salt (AgNO3) solution. Formation of nanoparticles was confirmed by UV-visible spectrometry. The surface plasmon resonance peak is located at 430 nm. Doping of silver nanoparticles (Ag NPs) with gelatin biopolymer was studied. The silver content in the polymer matrix was in the range of 0.4-1 wt%. The formation of nanoparticles disappeared for silver content higher than 1 wt%. The morphology and interaction of gelatin doped with Ag NPs was examined by transmission electron microscopy and FTIR spectroscopy. The content of Ag NPs has a pronounced effect on optical and structural properties of gelatin. Optical parameters such as refractive index, complex dielectric constant were calculated. The dispersion of the refractive index was discussed in terms of the single - oscillator Wemple-DiDomenico model. Color properties of the prepared samples were discussed in the framework of CIE L*u*v* color space.

Synthesis, morphological control, and antibacterial properties of hollow/solid Ag2S/Ag heterodimers

KAUST Repository

Pang, Maolin; Hu, Jiangyong; Zeng, Huachun

2010-01-01

of this highly asymmetric dipolar composite, photocatalytic inactivation of Escherichia coli K-12 in the presence of the as-prepared Ag 2S/Ag heterodimers has been carried out under UV irradiation. The added Ag2S/Ag heterodimers show good chemical stability under

108mAg and 110mAg in crassostrea gigas

International Nuclear Information System (INIS)

Ishikawa, Y.; Sato, N.; Nakamura, E.; Sekine, T.; Yoshihara, K.

1992-01-01

Accumulation of radiosilver 108m Ag and 110m Ag in oysters (Crassostrea gigas) and their behavior in marine environments has been studied in the northeast Pacific coast in Japan. Enrichment of radiosilver in oysters depends on topographical conditions; significant bioaccumulation occurred in open bays, while it was hardly observed in bays with narrow shaped entrances. From these observations difference of the behavior of radiosilver between open and nearly closed bays is suggested. 110m Ag in oysters decayed with an effective half-life of about 150 days for both the Chinese nuclear weapon test and the Chernobyl accident. In contrast to radiosilver, the fission product nuclide 137 Cs was almost independent of topographical conditions, and its concentration was constant. 110m Ag bioaccumulation in oysters after the Chernobyl accident in 1986 was found in both open and nearly closed bays, the lattershowing much lower concentration of radiosilver than the former. Specific activity of 108m Ag in oysters was determined in bays open to the Pacific Oceans. (author) 13 refs.; 4 figs.; 3 tabs

Studies on certain physical properties of modified smectite nanocatalysts

International Nuclear Information System (INIS)

Wu, Ming Ching; Kuo, Shu Lung; Lin, Jao Chuan; Ma, Chih Ming; Hong, Gui Bing; Chang, Chang Tang

2011-01-01

Most volatile organic compounds (VOCs) are toxic to humans in some manner. Generally, transitional metal catalysts have better conversion rates for controlling VOCs. However, catalyst activity will decay at high temperature, though the oxidizing catalyst is cheap. This study used smectite as the carrier to exchange with Ag + , Zn 2+ and Ti 4+ to modify the surface and form smectite catalysts. In addition, the transmission electron microscopy (TEM), FT-IR spectrum, and DSC-TGA instrument were applied to characterize their physical properties. After the FT-IR analysis of the modified smectite catalyst (smectite-Ag, smectite-Zn and smectite-Ti), both smectite and smectite catalyst had significant and complicated wave crests between the fingerprint area with the wave numbers of 415-600 cm -1 and 750-1170 cm -1 , that indicated the existence of a strong bond between impure silicates (Si-O) and silicates (O-Si-O). TEM observation proved that sintering at 350 deg. C results in the distribution of catalyst ions on clay carrier with a nanoscale. As thermal analysis reveals, the smectite reached endothermic peaks at the temperatures of 920 deg. C and 1057 deg. C, respectively, and shows the decomposition in a non-crystal form. Besides, the disappearance of the endothermic peak of smectite-Ag occurs at 920.5 deg. C and the exothermic peak occurs at 950 deg. C. The results indicating crystals formed of smectite-Ag are more comprehensive and stable than the other smectite or modified smectite catalysts at high temperature.

Secular distribution of highly metalliferous black shales corresponds with peaks in past atmosphere oxygenation

Science.gov (United States)

Johnson, Sean C.; Large, Ross R.; Coveney, Raymond M.; Kelley, Karen D.; Slack, John F.; Steadman, Jeffrey A.; Gregory, Daniel D.; Sack, Patrick J.; Meffre, Sebastien

2017-08-01

Highly metalliferous black shales (HMBS) are enriched in organic carbon and a suite of metals, including Ni, Se, Mo, Ag, Au, Zn, Cu, Pb, V, As, Sb, Se, P, Cr, and U ± PGE, compared to common black shales, and are distributed at particular times through Earth history. They constitute an important future source of metals. HMBS are relatively thin units within thicker packages of regionally extensive, continental margin or intra-continental marine shales that are rich in organic matter and bio-essential trace elements. Accumulation and preservation of black shales, and the metals contained within them, usually require low-oxygen or euxinic bottom waters. However, whole-rock redox proxies, particularly Mo, suggest that HMBS may have formed during periods of elevated atmosphere pO2. This interpretation is supported by high levels of nutrient trace elements within these rocks and secular patterns of Se and Se/Co ratios in sedimentary pyrite through Earth history, with peaks occurring in the middle Paleoproterozoic, Early Cambrian to Early Ordovician, Middle Devonian, Middle to late Carboniferous, Middle Permian, and Middle to Late Cretaceous, all corresponding with time periods of HMBS deposition. This counter-intuitive relationship of strongly anoxic to euxinic, localized seafloor conditions forming under an atmosphere of peak oxygen concentrations is proposed as key to the genesis of HMBS. The secular peaks and shoulders of enriched Se in sedimentary pyrite through time correlate with periods of tectonic plate collision, which resulted in high nutrient supply to the oceans and consequently maximum productivity accompanying severe drawdown into seafloor muds of C, S, P, and nutrient trace metals. The focused burial of C and S over extensive areas of the seafloor, during these anoxic to euxinic periods, likely resulted in an O2 increase in the atmosphere, causing short-lived peaks in pO2 that coincide with the deposition of HMBS. As metals become scarce, particularly Mo

Facile synthesis of AgCl/polydopamine/Ag nanoparticles with in-situ laser improving Raman scattering effect

Energy Technology Data Exchange (ETDEWEB)

Zhang, Yan; Zhang, Wenqi; Wang, Lin; Wang, Feng, E-mail: wangfeng@shnu.edu.cn; Yang, Haifeng

2017-01-15

Highlights: • AgCl/PDA/AgNPs (polydopamine (PDA) adlayer covered cubic AgCl core inlaid with Ag nanoparticles (AgNPs)) was fabricated for in-situ SERS detection. • Such SERS substrate shows in-situ laser improving Raman scattering effect due to the generation of more AgNPs. • Enhancement factor could reach 10{sup 7}. • Such SERS substrate shows good reproducibility and long term stability. - Abstract: We reported a simple and fast method to prepare a composite material of polydopamine (PDA) adlayer covered cubic AgCl core, which was inlaid with Ag nanoparticles (NPs), shortly named as AgCl/PDA/AgNPs. The resultant AgCl/PDA/AgNPs could be employed as surface-enhanced Raman scattering (SERS) substrate for in-situ detection and the SERS activity could be further greatly improved due to the production of more AgNPs upon laser irradiation. With 4-mercaptopyridine (4-Mpy) as the probe molecule, the enhancement factor could reach 10{sup 7}. Additionally, such SERS substrate shows good reproducibility with relative standard deviation of 7.32% and long term stability (after storage for 100 days under ambient condition, SERS intensity decay is less than 25%). In-situ elevating SERS activity of AgCl/PDA/AgNPs induced by laser may be beneficial to sensitive analysis in practical fields.

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.

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.

Effect of pH on optic and structural characterization of chemical deposited AgI thin films

Energy Technology Data Exchange (ETDEWEB)

Tezel, Fatma Meydaneri [Department of Metallurgy and Materials Engineering, Karabük University (Turkey); Kariper, İshak Afşin [Department of Science Education, Faculty of Education, Erciyes University, Kayseri (Turkey)

2017-11-15

AgI thin films were grown on amorphous commercial glass substrates with chemical bath deposition (CBD) at different pH values (2, 3, 4, 5, 6), 6 hours deposition time and 60 °C. The structure of the nanocrystals was characterized by X-ray diffraction (XRD). The ratio of Ag{sup +} and I{sup -} ions changed the crystalline structures. The presence of the Ag{sup +} ions produces the γ-phase of AgI and excess of iodine concentration produces β-phase of AgI. The pH: 4 was like a transition pH for these phases. The number of crystallites per unit area has maximum value at pH: 5, as the structure is re-crystallization to hexagonal phase. Also, the thicknesses of produced thin films were decreased with increased pH values. Therefore, transmission, reflection, extinction coefficients and refractive index of the materials were affected by thicknesses, and calculated to be 32, 35, 3, 11, 9 (%) - 27, 25, 61, 45, 49 (%) - 0.036, 0.032, 0.067, 0.107, 0.075 and 3.21, 3.02, 5.16, 8.35, 5.70 in 550 nm at pH: 2-3-4-5-6 values, respectively. The exciton peaks of AgI were observed at between 320 and 420 nm. Surface properties were investigated by using scanning electron microscopy (SEM). (author)

Small angle, quasielastic and inelastic neutron scattering from 0.85AgPO3-0.15PbI2 glass

International Nuclear Information System (INIS)

Malugani, J.P.; Tachez, M.; Mercier, R.

1987-01-01

A small angle neutron scattering (SANS) experiment and a quasielastic neutron scattering (QENS) experiment were performed on the fast ionic conductor 0.85AgPO 3 -0.15PbI 2 , which is a vitreous electrolyte. The SANS data show that the scattering obeys Guinier's law for Q -2 A; dispersed heterogeneities are present in the glass with a mean radius of gyration of 20 A. The QENS spectra show a quasielastic broadening of the elastic peak and a long tail up to 40 meV which is due to an inelastic distribution. The results seem to confirm the hypothesis on the structure of this glass: small 'clusters' of AgI with tetrahedral coordination are dispersed in the AgPO 3 host glass. In order to build these clusters, an exchange between Ag + and Pb 2+ is proposed. 18 refs.; 6 figs.; 2 tabs

Rape embryogenesis. IV. Appearance and disappearance of starch during embryo development

Directory of Open Access Journals (Sweden)

Teresa Tykarska

2014-01-01

Full Text Available Starch appears first in the suspensor of the proembryo with two-cell apical part. It is observed in the embryo proper from the octant stage. At first it is visible in all the embryo cells in the form of minute transient grains which disappear during cell divisions. But the columella mother cells and their derivatives have persistent large grains. When the embryo turns green in the heart stage a gradual accumulation of storage starch begins and lasts to the end of embryogenesis. Storage starch grains appear first in the auter cortex layers of the hypocotyl where the largest grains are to be found later, and afterwards in all the other tissues. Starch is usually absent in the frequently dividing cells, but even there it appears in the form of minute grains after the end of cell divisions. Disappearance of starch starts when the intensive green colour of the seed coat begins to fade. The first to disappear are the smallest granules in the regions where they were noted latest. In the embryo axis the starch grains remain deposited longest in dermatogen and cortex cells in the lower hypocotyl part. They are visible there, still when the seed turns brown. In black seeds starch may be only found in the columella the cells of which throughout embryogenesis contain amyloplasts filled with starch. These grains disappear completely at the time when the seeds become dry.

Reversible conversion between AgCl and Ag in AgCl-doped RSiO{sub 3/2}-TiO{sub 2} films prepared by a sol-gel technique

Energy Technology Data Exchange (ETDEWEB)

Kawamura, Go, E-mail: gokawamura@ee.tut.ac.jp [Department of Electrical and Electronic Information Engineering, Toyohashi University of Technology, Toyohashi, Aichi 441-8580 (Japan); Tsurumi, Yuuki [Department of Environmental and Life Sciences, Toyohashi University of Technology, Toyohashi, Aichi 441-8580 (Japan); Muto, Hiroyuki [Department of Electrical and Electronic Information Engineering, Toyohashi University of Technology, Toyohashi, Aichi 441-8580 (Japan); Department of Environmental and Life Sciences, Toyohashi University of Technology, Toyohashi, Aichi 441-8580 (Japan); Sakai, Mototsugu; Inoue, Mitsuteru [Department of Electrical and Electronic Information Engineering, Toyohashi University of Technology, Toyohashi, Aichi 441-8580 (Japan); Matsuda, Atsunori [Department of Electrical and Electronic Information Engineering, Toyohashi University of Technology, Toyohashi, Aichi 441-8580 (Japan); Department of Environmental and Life Sciences, Toyohashi University of Technology, Toyohashi, Aichi 441-8580 (Japan)

2011-10-17

Highlights: {center_dot} The reversible redox behavior between AgCl and Ag in RSiO{sub 3/2}-TiO{sub 2} film is studied. {center_dot} TiO{sub 2} component induces Cl to remain in the film after conversion of AgCl to Ag. {center_dot} The survival of Cl is essential for reconversion of Ag to AgCl. {center_dot} The film shows potential to be applied as rewritable holographic material. - Abstract: The reversible redox behavior exhibited by AgCl-doped organosilsesquioxane-titania gel films is studied. Films prepared by the sol-gel method show reversible color changes with blue laser irradiation and subsequent heat treatment, which is based on the formation of Ag and AgCl nanoparticles, respectively. Two-beam interference exposure experiments reveal that the films have potential to be applied as rewritable holographic materials. A large titania content is essential for the conversion of Ag to AgCl because it induces the Cl to remain near the Ag nanoparticles during blue laser irradiation, allowing the Cl to react with neighboring Ag nanoparticles to reform AgCl upon subsequent heat treatment.

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

Disappearing dark matter in brane world cosmology: New limits on noncompact extra dimensions

International Nuclear Information System (INIS)

Ichiki, K.; Garnavich, P.M.; Mathews, G.J.; Kajino, T.; Yahiro, M.

2003-01-01

We explore cosmological implications of dark matter as massive particles trapped on a brane embedded in a Randall-Sundrum noncompact higher dimension AdS 5 space. It is an unavoidable consequence of this cosmology that massive particles are metastable and can disappear into the bulk dimension. Here, we show that a massive dark matter particle (e.g. the lightest supersymmetric particle) is likely to have the shortest lifetime for disappearing into the bulk. We examine cosmological constraints on this new paradigm and show that disappearing dark matter is consistent (at the 95% confidence level) with all cosmological constraints, i.e., present observations of type Ia supernovae at the highest redshift, trends in the mass-to-light ratios of galaxy clusters with redshift, the fraction of x-ray emitting gas in rich clusters, and the spectrum of power fluctuations in the cosmic microwave background. A best 2σ concordance region is identified corresponding to a mean lifetime for dark matter disappearance of 15≤Γ -1 ≤80 Gyr. The implication of these results for brane-world physics is discussed

[Ag(NH3)2]Ag(OsO3N)2: a new nitridoosmate(VIII)

International Nuclear Information System (INIS)

Wickleder, M.S.; Pley, Martin

2004-01-01

Dark brown single crystals of [Ag(NH 3 ) 2 ]Ag(OsO 3 N) 2 were obtained from the reaction of Ag 2 CO 3 , OsO 4 , and NH 3 in aqueous solution. The crystal structure was solved in the monoclinic space group C2/m, with the following unit-cell dimensions: a=1962.5(3), b=633.1(1), c=812.6(1) pm, β=96.71(1) deg. The final reliability factor was R=0.0256 for 1034 reflections with I>2σ(I). Linear [Ag(NH 3 ) 2 ] + ions are present oriented perpendicular to the [010] direction, leading to short Ag + -Ag + distances of 316 pm. A second type of Ag + ions in the crystal structure present coordination number '6+1' and are surrounded by oxygen and nitrogen atoms of the nitridoosmate groups. Within the first of the two crystallographically distinguishable anions one can clearly differentiate between oxygen and nitrogen atoms while the second one exhibits a N/O disorder over two positions. The infrared spectrum of [Ag(NH 3 ) 2 ]Ag(OsO 3 N) 2 shows the typical absorptions which can be attributed to the complex anions and the NH 3 ligands

Microwave assisted facile synthesis of reduced graphene oxide-silver (RGO-Ag) nanocomposite and their application as active SERS substrate

International Nuclear Information System (INIS)

Wadhwa, Heena; Kumar, Devender; Mahendia, Suman; Kumar, Shyam

2017-01-01

The present paper represents the facile and rapid synthesis of reduced graphene oxide-silver (RGO-Ag) nanocomposite with the help of microwave irradiation. The graphene oxide (GO) solution has been prepared in bulk using Hummer's method followed by microwave assisted in-situ reduction of GO and silver nitrate (AgNO_3) by hydrazine hydrate in a short spam of 5 min. The prepared nanocomposite has been characterized using Transmission Electron Microscopy (TEM), X-Ray Diffraction (XRD) Scanning Electron Microscopy (SEM) and UV–Visible spectroscopy. TEM analysis shows that Ag nanoparticles with average size 32 nm are uniformly entangled with in RGO layers. The UV–Visible absorption spectrum of nanocomposite depicts the reduction of GO to RGO along with the formation of Ag nanoparticles with the presence of characteristic surface Plasmon resonance (SPR) peak of Ag nanoparticles at 422 nm. The performance of prepared nanocomposite has been tested as the active Surface Enhanced Raman Scattering (SERS) substrate for Rhodamine 6G with detection limit 0.1 μM. - Highlights: • The RGO and RGO-Ag nanocomposite were synthesized with microwave irradiation. • Ag nanoparticles of average size 32 nm are uniformly entangled within RGO layers. • RGO itself is a florescence quencher with SERS detection limit 1 μM for R6G. • RGO-Ag nanocomposite show good SERS activity for R6G with detection limit 0.1 μM.

AGS intensity record

International Nuclear Information System (INIS)

Bleser, Ed

1994-01-01

As flashed in the September issue, this summer the Brookhaven Alternating Gradient Synchrotron (AGS) reached a proton beam intensity of 4.05 x 10 13 protons per puise, claimed as the highest intensity ever achieved in a proton synchrotron. It is, however, only two-thirds of the way to its final goal of 6 x 10 13 . The achievement is the resuit of many years of effort. The Report of the AGS II Task Force, issued in February 1984, laid out a comprehensive programme largely based on a careful analysis of the PS experience at CERN. The AGS plan had two essential components: the construction of a new booster, and major upgrades to the AGS itself.

Study of Ag+/PAA (polyacrylic acid) and Ag0/PAA aqueous system at equilibrium

International Nuclear Information System (INIS)

Keghouche, N.; Mostafavi, M.; Delcourt, M.O.

1991-01-01

When submitted to gamma radiation the system Ag + -PAA-water leads to clusters Ag 0 n /PAA (3 420 nm) interacting with the clusters. Potentiometric measurements carried out on Ag + solutions in the presence of PAA at various pH show that the deprotonated form (polyacrylate anion) is strongly bonded to Ag + , on the opposite of the protonated form of PAA. One of the oligomer clusters can be stabilized for more than one year. Studying it by infra-red spectrometry reveals important modifications in the vibration bands of the COO - group circa 1400 and 1600 cm -1 according to the bonding of PAA with Ag + or Ag 0 [fr

Cytotoxicity of serum protein-adsorbed visible-light photocatalytic Ag/AgBr/TiO2 nanoparticles

International Nuclear Information System (INIS)

Seo, Ji Hye; Jeon, Won Il; Dembereldorj, Uuriintuya; Lee, So Yeong; Joo, Sang-Woo

2011-01-01

Highlights: ► Photocytotoxicity of visible-light catalytic NPs was examined in vitro. ► Ag/AgBr/TiO 2 NPs were well internalized in cells after adsorption of serum proteins. ► Cell viability was decreased by 40–60% using ∼8 ppm NPs and 60 W/cm 2 visible light within 5 h. ► Mitochondria activity test indicated the reactive oxygen species for photo-destruction of cells. ► Ag/AgBr/TiO 2 NPs were found to eliminate xenograft tumors significantly in vivo. - Abstract: Photocytotoxicity of visible-light catalytic Ag/AgBr/TiO 2 nanoparticles (NPs) was examined both in vitro and in vivo. The Ag/AgBr/TiO 2 NPs were prepared by the deposition–precipitation method. Their crystalline structures, atomic compositions, and light absorption property were examined by X-ray diffraction (XRD) patterns, X-ray photoelectron (XPS) intensities, and ultraviolet-visible (UV–vis) diffuse reflectance spectroscopic tools. The Ag/AgBr/TiO 2 NPs appeared to be well internalized in human carcinoma cells as evidenced by transmission electron microscopy (TEM). The cytotoxicity of cetylmethylammonium bromide (CTAB) appeared to be significantly reduced by adsorption of serum proteins in the cellular medium on the NP surfaces. Two types of human cervical HeLa and skin A431 cancer cells were tested to check their viability after the cellular uptake of the Ag/AgBr/TiO 2 NPs and subsequent exposure to an illumination of visible light from a 60 W/cm 2 halogen lamp. Fluorescence images taken to label mitochondria activity suggest that the reactive oxygen species should trigger the photo-destruction of cancer cells. After applying the halogen light illumination for 50–250 min and ∼8 ppm (μg/mL) of photocatalytic Ag/AgBr/TiO 2 NPs, we observed a 40–60% selective decrease of cell viability. Ag/AgBr/TiO 2 NPs were found to eliminate xenograft tumors significantly by irradiating visible light in vivo for 10 min.

Seasonal ataxia: a case report of a disappearing disease

African Journals Online (AJOL)

Seasonal ataxia: a case report of a disappearing disease. Adebiyi Ayoade ... ological profiles of the disease. ... low serum albumin levels [8] act as a potentiating factor to trigger the ... 65% neutrophils, 25% lymphocytes,eosinophils 5% and.

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.

Synthesis of gold nanorods with a longitudinal surface plasmon resonance peak of around 1250 nm

Science.gov (United States)

Nguyen, Thi Nhat Hang; Le Trinh Nguyen, Thi; Thanh Tuyen Luong, Thi; Thang Nguyen, Canh Minh; Nguyen, Thi Phuong Phong

2016-03-01

We prepared gold nanorods and joined them to chemicals such as tetrachloauric (III) acid trihydrate, silver nitrate, hydroquinone, hexadecyltrimethylammonium bromide, sodium hydroxide and sodium borohydride using the seed-mediated method. The combination of hydroquinone, with or without salicylic acid, influences the size of the gold nanorods, and this is demonstrated by the results of TEM images, UV-vis spectra and the value of the longitudinal surface plasmon resonance peak with respect to the UV-vis spectra. By changing the Ag+ ion and hydroquinone concentration and the combination of hydroquinone and salicylic acid, the size of the gold nanorods can be controlled and this is manifested by longitudinal surface plasmon resonance peaks forming between 875 and 1278 nm. In particular, sample E2 achieved a longitudinal surface plasmon peak at 1273 nm and an aspect ratio of more than 10 by modifying the hydroquinone to 2.5 mM and salicylic acid to 0.5 mM concentration in the growth solution.

Replacement of Poly(vinyl pyrrolidone) by Thiols: A Systematic Study of Ag Nanocube Functionalization by Surface-Enhanced Raman Scattering.

Science.gov (United States)

Moran, Christine H; Rycenga, Matthew; Zhang, Qiang; Xia, Younan

2011-11-10

In this work, we used surface-enhanced Raman scattering (SERS) to monitor the replacement of poly(vinyl pyrrolidone) (PVP) on Ag nanocubes by cysteamine, thiol-terminated PEG, and benzenedithiol. PVP is widely used as a colloidal stabilizer and capping agent to control the shape of Ag (as well as many other noble metals) nanocrystals during synthesis, and to stabilize the final colloidal suspension. However, the surface chemistry of Ag nanocrystals often needs to be tailored for specific applications, so the PVP coating must be removed and/or replaced by other ligands. By monitoring the signature peak from the carbonyl groups of PVP, we show, for the first time, that the PVP adsorbed on the surface of Ag nanocubes was completely replaced by the thiol molecules at room temperature over the course of a few hours. We observed the same trend no matter if the Ag nanocubes were suspended in an aqueous solution of the thiol or supported on a silicon substrate and then immersed in the thiol solution.

Occurrence of two-photon absorption saturation in Ag nanocolloids, prepared by chemical reduction method

Energy Technology Data Exchange (ETDEWEB)

Rahulan, K. Mani, E-mail: krahul.au@gmail.com [Department of Physics, Anna University, Chennai (India); Ganesan, S. [Department of Physics, Anna University, Chennai (India); Aruna, P., E-mail: aruna@annauniv.edu [Department of Physics, Anna University, Chennai (India)

2012-09-01

Highlights: Black-Right-Pointing-Pointer Ag nanocolloids were synthesized via chemical reduction method. Black-Right-Pointing-Pointer The molecules of PVP play an important role in growth and agglomeration of silver nanocolloids. Black-Right-Pointing-Pointer Saturation behaviour followed by two photon absorption was responsible for good optical limiting characteristics in these nanocolloids. Black-Right-Pointing-Pointer The nonlinear optical parameters calculated from the data showed that these materials could be used as efficient optical limiters. - Abstract: Silver nanocolloids stabilized with polyvinyl pyrrolidone (PVP) have been prepared from (AgNO{sub 3}) by a chemical reduction method, involving the intermediate preparation of (Ag{sub 2}O) colloidal dispersions in the presence of sodium dodecycle sulfate as a surfactant and formaldehyde as reducing agent. The molecules of PVP play an important role in growth and agglomeration of silver nanocolloids. The formation of Ag nanocolloids was studied from the UV-vis absorption characteristics. An energy dispersive X-ray (EDX) spectrum and X-ray diffraction peak of the nanoparticles showed the highly crystalline nature of silver structure. The particle size was found to be 40 nm as analyzed from Field emission scanning electron microscopy (FESEM). The nonlinear optical and optical limiting properties of these nanoparticle dispersions were studied by using the Z-scan technique at 532 nm. Experimental results show that the Ag nanocolloids possess strong optical limiting effect, originated from absorption saturation followed by two-photon mechanism. The data show that Ag nanocolloids have great potential for nonlinear optical devices.

Direct inelastic scattering of oriented NO from Ag(111) and Pt(111)

International Nuclear Information System (INIS)

Tenner, M.G.; Kuipers, E.W.; Kleyn, A.W.; Stolte, S.

1991-01-01

A pulsed supersonic and cold oriented beam of NO molecules is incident upon the (111) face of clean Ag and Pt single crystal surfaces. The steric effect in the scattered density distributions is determined by a quadrupole mass spectrometer. It is found that the steric effect in the peak in the distribution of direct inelastically scattered molecules depends linearly on the reflection angle. In all circumstances O-end collisions lead to scattering angles more inclined towards the surface than N-end collisions. For the Pt(111) surface a much stronger steric effect is measured than for the Ag(111) surface. The steric effect seems to scale with the incident normal velocity. These strong steric effects can be explained by the larger trapping probability for the N-end orientation and a leverage effect due to the high trapping probability

Role of catalytic protein and stabilising agents in the transformation of Ag ions to nanoparticles by Pseudomonas aeruginosa.

Science.gov (United States)

Ali, Jafar; Hameed, Abdul; Ahmed, Safia; Ali, Muhammad Ishtiaq; Zainab, Shama; Ali, Naeem

2016-10-01

Biological routes of synthesising metal nanoparticles (NPs) using microbes have been gaining much attention due to their low toxicity and eco-friendly nature. Pseudomonas aeruginosa JP2 isolated from metal contaminated soil was evaluated towards extracellular synthesis of silver NPs (AgNPs). Cell-free extract (24 h) of the bacterial isolate was reacted with AgNO 3 for 24 h in order to fabricate AgNPs. Preliminary observations were recorded in terms of colour change of the reaction mixture from yellow to greyish black. UV-visible spectroscopy of the reaction mixture has shown a progressive increase in optical densities that correspond to peaks near 430 nm, depicting reduction of ionic silver (Ag + ) to atomic silver (Ag 0 ) thereby synthesising NPs. X-ray diffraction spectra exhibited the 2θ values to be 38.4577° confirming the crystalline and spherical nature of NPs [9.6 - 26.7 (Ave. = 17.2 nm)]. Transmission electron microscopy finally confirmed the size of the particles varying from 5 to 60 nm. Moreover, rhamnolipids and proteins were identified as stabilising molecules for the AgNPs through Fourier transform-infrared spectroscopy. Characterisation of bacterial crude and purified protein fractions confirmed the involvement of nitrate reductase (molecular weight 66 kDa and specific activity = 3.8 U/mg) in the Synthesis of AgNPs.

Nuclear relaxation phenomena, diffusion and orbiting in the reaction 107109Ag + 8486Kr at 7.2 MeV/nucleon

International Nuclear Information System (INIS)

Schmitt, R.P.; Russo, P.; Babinet, R.; Jared, R.; Moretto, L.G.

1977-01-01

Charged particles produced from the interaction of a 7.2 MeV/nucleon Kr beam and a natural Ag target have been studied. Fragments up to Z = 50 have been identified by means of a ΔE, E telescope. Kinetic energy distributions, charge distributions and angular distributions have been measured for the individual atomic numbers. The kinetic energy distributions show two components: a high energy 'quasi-elastic' component, and a low energy or 'relaxed' component close to the Coulomb energy for touching spheres. The charge distribution for this system is very broad and appears to peak at symmetry rather than at the Z of the projectile. The angular distributions for the relaxed component increase monotonically with decreasing angle and are all forward peaked in excess of 1/sintheta. These results are dramatically different from those obtained in Kr bombardments of heavier targets where rather narrow charge distributions and side peaked angular distributions have been observed. The behavior of the reaction Ag+Kr is strongly reminiscent of reactions induced by lighter projectiles. An interpretation of these data in terms of a diffusion process along the mass asymmetry coordinate is presented. (Auth.)

The effect of Ag and Ca additions on the age hardening response of Mg–Zn alloys

International Nuclear Information System (INIS)

Bhattacharjee, T.; Mendis, C.L.; Oh-ishi, K.; Ohkubo, T.; Hono, K.

2013-01-01

The effect of sole and combined additions of Ag and Ca in enhancing the age hardening response in a Mg–2.4Zn (at%) alloy have been studied by systematic microstructure investigations using transmission electron microscopy (TEM) and three dimensional atom probe (3DAP). In the early aging stage of a Mg–2.4Zn–0.1Ag–0.1Ca (at%) alloy at 160 °C, Zn-rich Guinier Preston (G.P.) zones form with Ag and Ca enrichment. Further aging lead to the formation of fine β′ 1 precipitates with Ag and Ca enrichment. We confirmed that the G.P. zones do not form in the Mg–2.4Zn (at%) binary alloy at 160 °C, but form after a prolonged aging at 70 °C. This suggests that the combined addition of Ag and Ca shifts the metastable solvus for the G.P. zones to a higher temperature, thereby making it possible to form G.P. zones even at the artificial aging temperature of 160 °C. Since G.P. zones act as nucleation sites for the β′ 1 precipitates, the peak-aged microstructure is refined substantially by the addition of Ag and Ca

Ag-rich precipitates formation in the Cu–11%Al–10%Mn–3%Ag alloy

Energy Technology Data Exchange (ETDEWEB)

Silva, R.A.G., E-mail: galdino.ricardo@gmail.com [Departamento de Ciências Exatas e da Terra, UNIFESP, 09972-270 Diadema, SP (Brazil); Paganotti, A.; Jabase, L. [Departamento de Ciências Exatas e da Terra, UNIFESP, 09972-270 Diadema, SP (Brazil); Adorno, A.T.; Carvalho, T.M.; Santos, C.M.A. [Departamento de Físico-Química, Instituto de Química, UNESP, 14801-970 Araraquara, SP (Brazil)

2014-12-05

Highlights: • Cu-rich nanoprecipitates are formed in the presence of Ag. • Bainite precipitation is shifted to higher temperatures in the Cu–11%Al–10%Mn–3%Ag alloy. • The eutectoid α phase and bainite α{sub 1} phase compete by the Cu atoms during precipitation process. - Abstract: The formation of Ag-rich precipitates in the Cu–11%Al–10%Mn–3%Ag alloy initially quenched from 1123 K was analyzed. The results showed that nanoprecipitates of a Cu-rich phase are produced at about 523 K. In higher temperatures these nanoparticles grow and the relative fraction of Ag dissolved in it is increased, thus forming the Ag-rich phase.

Morphological, Structural and Optical Evolution of Ag Nanostructures on c-Plane GaN Through the Variation of Deposition Amount and Temperature

Science.gov (United States)

Sui, Mao; Li, Ming-Yu; Pandey, Puran; Zhang, Quanzhen; Kunwar, Sundar; Lee, Jihoon

2018-03-01

Owing to their tunable properties, Ag nanostructures have been widely adapted in various applications and the morphological control can determine their performance and effectiveness. In this work, we demonstrate the morphological and optical evolution of Ag nanostructures on GaN (0001) by the systematic control of deposition amount at two distinctive annealing temperatures. Based on the Volmer-Weber and coalescence growth models, the nanostructure growth commenced by the thermal solid-state-dewetting evolve in terms of size, density and configuration. At 450 °C, the round-dome shaped Ag nanoparticles (regime I), irregular Ag nano-mounds (regime II) and void-layer structures (regime III) are observed along with the gradually increased deposition amount. As a sharp distinction, the solid state dewetting process occur more radically at 700 °C and also, the Ag sublimation and the effect on the nanostructure formation are observed in a clear regime shift scaled by the deposition amount. Meanwhile, a strong dependency of reflectance spectra evolution on the Ag nanostructure morphology is witnessed for both sets. In particular, Ag dipolar resonance peaks are significantly red-shifted from VIS to NIR regions along with the nanostructure evolution. The reflectance, PL and Raman intensity variation are also observed and discussed based on the evolution of Ag nanostructures.

Tollen’s reagent assisted synthesis of hollow polyaniline microsphere/Ag nanocomposite and its applications in sugar sensing and electromagnetic shielding

Energy Technology Data Exchange (ETDEWEB)

Panigrahi, R.; Srivastava, S.K., E-mail: sunit@chem.iitkgp.ernet.in

2015-04-15

Graphical abstract: Probable scheme to demonstrate the mechanism of PnHMAg showing enhanced EMI shielding compared to PnHM. - Highlights: • Hollow polyaniline microsphere (PnHM) exhibits superior properties due to its enhanced surface to volume ratio. • PnHMAg has been used in developing efficient sensor for the detection of sugar. • Presence of Ag nanoparticles enhances the electrical conductivity of PnHMAg resulting in the improvement of electromagnetic interference shielding in both X- and S-band regions. • Such properties could be harnessed effectively for development of devices for commercial as well as national purposes. - Abstract: The present study is focused on synthesis of polyaniline hollow microspheres (PnHM) nanocomposites of silver (Ag) i.e., PnHMAg by emulsion polymerization of aniline and Tollen’s reagent as a source for Ag nanoparticles. X-ray diffraction (XRD) and transmission electron microscopy (TEM) analysis of PnHMAg indicated presence of silver nanoparticles dispersed on polyaniline surface. The electrical conductivity of PnHMAg is increased by ∼6 times compared to PnHM. Cyclic voltammogram of PnHM in sugar sensing exhibits characteristics redox peaks at ∼0.09 (sugar) and ∼0.53 V (polyaniline). Interestingly, PnHMAg showed a single peak at ∼−0.18 V with increased intensity (∼5 times) indicating its high sugar sensing ability. PnHMAg also exhibits high shielding efficiency of 19.5 dB (11.2 GHz) due to the presence of highly conducting Ag nanoparticles. TEM studies confirmed that Ag nanoparticles are well distributed on PnHM. As a result, a continuous electronic path is developed due to enhanced interconnectivity of PnHM.

Nature of the precipitate in (AgI)0.7(AgPO3)0.3 glass

International Nuclear Information System (INIS)

Kartini, E.; Collins, M.F.

1999-01-01

Complete text of publication follows. Interest of this material arises from its superionic conducting properties, i.e. the conductivity at ambient temperature is a few order of magnitudes larger than in the pure AgI. On quenching the molten miacture from 600 deg C into liquid nitrogen, β-AgI crystal precipitates in the glassy matrix. Neutron powder diffraction studies on (AgI) 0.7 (AgPO 3 ) 0.3 are presented and the powder pattern from the crystalline precipitate is compared with that of pure AgI. The measurements show identical diffraction patterns from the precipitate and from β-AgI with the same lattice parameters. On heating, the precipitate shows a β→α phase transformation at 435 K while AgI shows this transformation at 438 K. At higher temperature in the α phase the powder pattern of the precipitate is again the same as that of pure α-AgI. On cooling the reverse transformation takes place at 415 K and 410 K, respectively. It is concluded that the precipitate is more-or-less pure AgI. (author)

Synthesis and characterization of Ag/AgBrO{sub 3} photocatalyst with high photocatalytic activity

Energy Technology Data Exchange (ETDEWEB)

Song, Limin, E-mail: songlmnk@sohu.com [College of Environment and Chemical Engineering & State Key Laboratory of Hollow-Fiber Membrane Materials and Membrane Processes, Tianjin Polytechnic University, Tianjin, 300387 (China); Li, Tongtong [College of Environment and Chemical Engineering & State Key Laboratory of Hollow-Fiber Membrane Materials and Membrane Processes, Tianjin Polytechnic University, Tianjin, 300387 (China); Zhang, Shujuan [College of Science, Tianjin University of Science & Technology, Tianjin, 300457 (China)

2016-10-01

A new Ag/AgBrO{sub 3} photocatalyst was prepared by mixing aqueous solutions of AgNO{sub 3} and NaBrO{sub 3}. The catalyst’s structure and performance were investigated with X-ray powder diffraction, transmission electron microscopy, and X-ray photoelectron spectroscopy. The UV–vis absorption spectrum of Ag/AgBrO{sub 3} exhibits a band gap of 3.97 eV. The results show that the Ag/AgBrO{sub 3} semiconductor can be excited by ultraviolet–visible light. The photodegradation of Rhodamine B displayed much higher photocatalytic activity than that of N-doped TiO{sub 2} under the same experimental conditions. Moreover, ·OH and ·O{sub 2}{sup −} generated in the photocatalysis played a key role of the photodegradation of Rhodamine B. - Highlights: • Ag/AgBrO{sub 3} with higher photodegradation ability was synthesized. • ·OH and ·O{sub 2}{sup −} radicals were the main active species in the oxidation of RhB. • The possible reaction mechanism was discussed in details.

Effect of cysteine and humic acids on bioavailability of Ag from Ag nanoparticles to a freshwater snail

Science.gov (United States)

Luoma, Samuel N.; Tasha Stoiber,; Croteau, Marie-Noele; Isabelle Romer,; Ruth Merrifeild,; Lead, Jamie

2016-01-01

Metal-based engineered nanoparticles (NPs) will undergo transformations that will affect their bioavailability, toxicity and ecological risk when released to the environment, including interactions with dissolved organic material. The purpose of this paper is to determine how interactions with two different types of organic material affect the bioavailability of silver nanoparticles (AgNPs). Silver uptake rates by the pond snail Lymnaea stagnalis were determined after exposure to 25 nmol l-1 of Ag as PVP AgNPs, PEG AgNPs or AgNO3, in the presence of either Suwannee River humic acid or cysteine, a high-affinity thiol-rich organic ligand. Total uptake rate of Ag from the two NPs was either increased or not strongly affected in the presence of 1 – 10 mg 1-1 humic acid. Humic substances contain relatively few strong ligands for Ag explaining their limited effects on Ag uptake rate. In contrast, Ag uptake rate was substantially reduced by cysteine. Three components of uptake from the AgNPs were quantified in the presence of cysteine using a biodynamic modeling approach: uptake of dissolved Ag released by the AgNPs, uptake of a polymer or large (>3kD) Ag-cysteine complex and uptake of the nanoparticle itself. Addition of 1:1 Ag:cysteine reduced concentrations of dissolved Ag, which contributed to, but did not fully explain the reductions in uptake. A bioavailable Ag-cysteine complex (> 3kD) appeared to be the dominant avenue of uptake from both PVP AgNPs and PEG AgNPs in the presence of cysteine. Quantifying the different avenues of uptake sets the stage for studies to assess toxicity unique to NPs.

Highly sensitive and stable Ag@SiO2 nanocubes for label-free SERS-photoluminescence detection of biomolecules

Science.gov (United States)

Nguyen, Minh-Kha; Su, Wei-Nien; Chen, Ching-Hsiang; Rick, John; Hwang, Bing-Joe

2017-03-01

Surface-enhanced Raman scattering (SERS) and fluorescence microscopy are a widely used biological and chemical characterization techniques. However, the peak overlapping in multiplexed experiments and rapid photobleaching of fluorescent organic dyes is still the limitations. When compared to Ag nanocubes (NCs), higher SERS sensitivities can be obtained with thin shelled silica Ag@SiO2 NCs, in contrast metal-enhanced photoluminescence (MEPL) is only found with NCs that have thicker silica shells. A 'dual functionality' represented by the simultaneous strengthening of SERS and MEPL signals can be achieved by mixing Ag@SiO2 NCs, with a silica shell thickness of 1.5 nm and 4.4 nm. This approach allows both the Ag@SiO2 NCs SERS and MEPL sensitivities to be maintained at 90% after 12 weeks of storage. Based on the distinguished detection of creatinine and flavin adenine dinucleotide in the mixture, the integration of SERS and MEPL together on a stable single plasmonic nanoparticle platform offers an opportunity to enhance both biomarker detection sensitivity and specificity.

The disappearance of Sphagnum imbricatum from Butterburn Flow, UK

NARCIS (Netherlands)

McClymont, E.L.; Mauquoy, D.; Yeloff, D.; Broekens, P.; van Geel, B.; Charman, D.J.; Pancost, R.D.; Chambers, F.M.; Evershed, R.P.

2008-01-01

The disappearance of the previously abundant moss species Sphagnum imbricatum has been investigated at Butterburn Flow, northern England, using organic geochemical, elemental, macrofossil, pollen and testate amoebae analyses. Variations in the assemblage of peat-forming plants were tracked using the

The timing and spatiotemporal patterning of Neanderthal disappearance.

Science.gov (United States)

Higham, Tom; Douka, Katerina; Wood, Rachel; Ramsey, Christopher Bronk; Brock, Fiona; Basell, Laura; Camps, Marta; Arrizabalaga, Alvaro; Baena, Javier; Barroso-Ruíz, Cecillio; Bergman, Christopher; Boitard, Coralie; Boscato, Paolo; Caparrós, Miguel; Conard, Nicholas J; Draily, Christelle; Froment, Alain; Galván, Bertila; Gambassini, Paolo; Garcia-Moreno, Alejandro; Grimaldi, Stefano; Haesaerts, Paul; Holt, Brigitte; Iriarte-Chiapusso, Maria-Jose; Jelinek, Arthur; Jordá Pardo, Jesús F; Maíllo-Fernández, José-Manuel; Marom, Anat; Maroto, Julià; Menéndez, Mario; Metz, Laure; Morin, Eugène; Moroni, Adriana; Negrino, Fabio; Panagopoulou, Eleni; Peresani, Marco; Pirson, Stéphane; de la Rasilla, Marco; Riel-Salvatore, Julien; Ronchitelli, Annamaria; Santamaria, David; Semal, Patrick; Slimak, Ludovic; Soler, Joaquim; Soler, Narcís; Villaluenga, Aritza; Pinhasi, Ron; Jacobi, Roger

2014-08-21

The timing of Neanderthal disappearance and the extent to which they overlapped with the earliest incoming anatomically modern humans (AMHs) in Eurasia are key questions in palaeoanthropology. Determining the spatiotemporal relationship between the two populations is crucial if we are to understand the processes, timing and reasons leading to the disappearance of Neanderthals and the likelihood of cultural and genetic exchange. Serious technical challenges, however, have hindered reliable dating of the period, as the radiocarbon method reaches its limit at ∼50,000 years ago. Here we apply improved accelerator mass spectrometry (14)C techniques to construct robust chronologies from 40 key Mousterian and Neanderthal archaeological sites, ranging from Russia to Spain. Bayesian age modelling was used to generate probability distribution functions to determine the latest appearance date. We show that the Mousterian ended by 41,030-39,260 calibrated years bp (at 95.4% probability) across Europe. We also demonstrate that succeeding 'transitional' archaeological industries, one of which has been linked with Neanderthals (Châtelperronian), end at a similar time. Our data indicate that the disappearance of Neanderthals occurred at different times in different regions. Comparing the data with results obtained from the earliest dated AMH sites in Europe, associated with the Uluzzian technocomplex, allows us to quantify the temporal overlap between the two human groups. The results reveal a significant overlap of 2,600-5,400 years (at 95.4% probability). This has important implications for models seeking to explain the cultural, technological and biological elements involved in the replacement of Neanderthals by AMHs. A mosaic of populations in Europe during the Middle to Upper Palaeolithic transition suggests that there was ample time for the transmission of cultural and symbolic behaviours, as well as possible genetic exchanges, between the two groups.

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.

Structural and optical properties of ZnO nanostructures electrochemically synthesized on AZO/Ag/AZO-multilayer-film-coated polyethersulfone substrates

International Nuclear Information System (INIS)

Oh, Dohyun; Yoo, Chanho; No, Youngsoo; Kim, Suyoun; Kim, Taewhan; Cho, Woonjo; Kim, Jinyoung

2012-01-01

ZnO nanostructures were formed on Al-doped ZnO (AZO)/Ag/AZO-multilayer-film-coated flexible polyethersulfone (PES) substrates at low temperature by using an electrochemical deposition method. The resistivity of the AZO/Ag/AZO multilayer films decreased with increasing thickness of the Ag film. X-ray diffraction patterns for the ZnO nanostructures showed that the crystal structure of the ZnO was hexagonal wurtzite and that the orientation was along the c-axis perpendicular to the substrate. Scanning electron microscopy images showed that the ZnO nanostructures grown at current densities of - 1.0 and - 1.5 mA/cm 2 were ZnO nanorods with diameters of 150 nm and ZnO nanoflowers with a planar dimension, respectively. Photoluminescence spectra showed that the band-edge emission peak of the ZnO nanostructures dominantly appeared in the ultraviolet region. These results showed that ZnO nanorods and nanoflowers with high quality were synthesized on AZO/Ag/AZO-multilayer-film-coated PES substrates.

Room temperature synthesis and photocatalytic property of AgO/Ag2Mo2O7 heterojunction nanowires

International Nuclear Information System (INIS)

Hashim, Muhammad; Hu, Chenguo; Wang, Xue; Wan, Buyong; Xu, Jing

2012-01-01

Graphical abstract: The AgO nanoparticles are attached on the surface of the Ag 2 Mo 2 O 7 nanowires to form a heterojunction structure. The AgO nanoparticles start embedding into the nanowires with increasing reaction temperature or time. Highlights: ► AgO/Ag 2 Mo 2 O 7 heterojunction NWs were synthesized at room temperature for the first time. ► AgO particles embed into the Ag 2 Mo 2 O 7 NWs with increase in reaction time and temperature. ► The heterojunction NWs display much better photocatalytic activity than the none-heterojunction NWs. ► The catalytic mechanism was proposed. -- Abstract: AgO/Ag 2 Mo 2 O 7 heterojunction nanowires were synthesized at temperatures of 25 °C, 50 °C, 80 °C, and 110 °C, under magnetic stirring in solution reaction. The catalytic activity of AgO/Ag 2 Mo 2 O 7 nanowires was evaluated by the degradation of Rhodmine B dye under the irradiation of the simulated sunlight. The synthesized samples were characterized by X-ray diffractometer, energy dispersive spectrometry, X-ray photoelectron spectrometer, scanning electron microscopy, and transmission electron microscopy. The results show that the AgO nanoparticles are attached on the surface of the Ag 2 Mo 2 O 7 nanowires to form a heterojunction structure. The length of the nanowires is up to 10 μm and the size of the AgO nanoparticles is 10–20 nm. The length of nanowires increases with increasing reaction time and temperature while the AgO particles are gradually embedded into the nanowires. The photocatalytic activity is greatly improved for the AgO/Ag 2 Mo 2 O 7 heterojunction nanowires compared with that of the pure Ag 2 Mo 2 O 7 nanowires, indicating a remarkable role of AgO particles on the Ag 2 Mo 2 O 7 nanowires in the photodegradation.

Ag@Ag_8W_4O_1_6 nanoroasted rice beads with photocatalytic, antibacterial and anticancer activity

International Nuclear Information System (INIS)

Selvamani, Muthamizh; Krishnamoorthy, Giribabu; Ramadoss, Manigandan; Sivakumar, Praveen Kumar; Settu, Munusamy; Ranganathan, Suresh; Vengidusamy, Narayanan

2016-01-01

Increasing resistance of pathogens and cancer cell line towards antibiotics and anticancer agents has caused serious health problems in the past decades. Due to these problems in recent years, researchers have tried to combine nanotechnology with material science to have intrinsic antimicrobial and anticancer activity. The metals and metal oxides were investigated with respect to their antimicrobial and anticancer effects towards bacteria and cancer cell line. In the present work metal@metal tungstate (Ag@Ag_8W_4O_1_6 nanoroasted rice beads) is investigated for antibacterial activity against Escherichia coli and Staphylococcus aureus using Mueller-Hinton broth and the anticancer activity against B16F10 cell line was studied. Silver decorated silver tungstate (Ag@Ag_8W_4O_1_6) was synthesized by the microwave irradiation method using Cetyl Trimethyl Ammonium Bromide (CTAB). Ag@Ag_8W_4O_1_6 was characterized by using various spectroscopic techniques. The phase and crystalline nature were analyzed by using XRD. The morphological analysis was carried out using Field Emission Scanning Electron Microscopy (FE-SEM), and High Resolution Transmission Electron Microscopy (HR-TEM). Further, Fourier Transform Infrared Spectroscopy (FT-IR) and Raman spectral analysis were carried out in order to ascertain the presence of functional groups in Ag@Ag_8W_4O_1_6. The optical property was investigated using Diffuse Reflectance Ultraviolet–Visible Spectroscopy (DRS-UV–Vis) and the band gap was found to be 3.08 eV. Surface area of the synthesized Ag@Ag_8W_4O_1_6 wasanalyzed by BET analysis and Ag@Ag_8W_4O_1_6 was utilized for the degradation of organic dyes methylene blue and rhodamine B. The morphology of the Ag@Ag_8W_4O_1_6 resembles roasted rice beads with breath and length in nm range. The oxidation state of tungsten (W) and silver (Ag) was investigated using X-ray photoelectron spectroscopy (XPS). - Highlights: • Synthesis of Ag@Ag_8W_4O_1_6 nanoroasted rice beads using

AGS intensity upgrades

International Nuclear Information System (INIS)

Roser, T.

1995-01-01

After the successful completion of the AGS Booster and several upgrades of the AGS, a new intensity record of 6.3 x 10 13 protons per pulse accelerated to 24 GeV was achieved. The high intensity slow-extracted beam program at the AGS typically serves about five production targets and about eight experiments including three rare Kaon decay experiments. Further intensity upgrades are being discussed that could increase the average delivered beam intensity by up to a factor of four

Bifunctional Ag@Pd-Ag Nanocubes for Highly Sensitive Monitoring of Catalytic Reactions by Surface-Enhanced Raman Spectroscopy.

Science.gov (United States)

Li, Jumei; Liu, Jingyue; Yang, Yin; Qin, Dong

2015-06-10

We report a route to the facile synthesis of Ag@Pd-Ag nanocubes by cotitrating Na2PdCl4 and AgNO3 into an aqueous suspension of Ag nanocubes at room temperature in the presence of ascorbic acid and poly(vinylpyrrolidone). With an increase in the total titration volume, we observed the codeposition of Pd and Ag atoms onto the edges, corners, and side faces of the Ag nanocubes in a site-by-site fashion. By maneuvering the Pd/Ag ratio, we could optimize the SERS and catalytic activities of the Ag@Pd-Ag nanocubes for in situ SERS monitoring of the Pd-catalyzed reduction of 4-nitrothiophenol by NaBH4.

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.

Influence of Doppler and 'Stark' effects on the shape of the autoionization peaks in electron energy spectra produced in ion-atom collisions

International Nuclear Information System (INIS)

Gleizes, A.; Benoit-Cattin, P.; Bordenave-Montesquieu, A.; Merchez, H.

1976-01-01

A detailed study is given of the influence of the Doppler shift and broadening on the spectra of electrons ejected by autoionization in collisions between heavy particles. General formulae have been obtained which permit the validity of results already published by other authors to be discussed. These results have been applied to the spectra of electrons ejected in He + -He collisions at 15 keV. The variation of the width of the autoionization peaks against ejection angle is well explained by Doppler broadening. On the contrary, the shape of these peaks cannot be due to the Doppler effect but rather to the Stark effect which is also studied in various experimental cases; it has been verified that the latter effect disappears in collisions between neutral particles for which symmetric peaks at 15 keV are obtained. (author)

Hierarchical Ag/AgCl-TiO{sub 2} hollow spheres with enhanced visible-light photocatalytic activity

Energy Technology Data Exchange (ETDEWEB)

Wang, Xu Long; Yin, Hao Yong [College of Materials Environment Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China); Nie, Qiu Lin, E-mail: nieqiulin@hdu.edu.cn [College of Materials Environment Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China); Wu, Wei Wei [College of Materials Environment Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China); Zhang, Yang; LiYuan, Qiu [College of Science, Hangzhou Dianzi University, Hangzhou 310018 (China)

2017-01-01

The hierarchical Ag/AgCl-TiO{sub 2} hollow spheres were synthesized by depositing Ag/AgCl nanoparticles on TiO{sub 2} hollow spheres via a precipitation photoreduction method, and they were further characterized using TGA, SEM, TEM, XRD, XPS, UV–vis DRS and photoelectric chemical analysis. The analysis showed that the hierarchical Ag/AgCl-TiO{sub 2} hollow spheres exhibited the highest photocatalytic activity, which was approximately 13 times higher than that of TiO{sub 2} hollow spheres. The high photocatalytic activity of the composites is due to efficient electron-hole pairs separation at the photocatalyst interfaces, and localized surface plasmon resonance of Ag nanoparticles formed on AgCl particles in the degradation reaction. - Highlights: • TiO{sub 2} hollow spheres were prepared by a sacrificial template method. • The hollow spheres were modified with Ag/AgCl to form the heterojunctions. • The modification may produce synergistic effect of LSPR and hollow structure. • Visible light photocatalytic activity was enhanced on this hollow catalyst. • The mechanism of the improved photocatalytic performance was discussed.

Removal of Ag+ from water environment using a novel magnetic thiourea-chitosan imprinted Ag+

International Nuclear Information System (INIS)

Fan, Lulu; Luo, Chuannan; Lv, Zhen; Lu, Fuguang; Qiu, Huamin

2011-01-01

Highlights: → Coating modified chitosan on magnetic fluids, which were using Ag(I) as imprinted ions, is a new method to expand function of the chitosan. → The method can improve the surface area for adsorption of Ag + and reduce the required dosage for the adsorption of Ag(I). → The imprinted magnetic chitosan can be used effectively and selectively to remove Ag(I) ions from aqueous solutions. → It shows the facile, fast separation process of magnetic chitosan during the experiments. The absorbent has a good application prospect. - Abstract: A novel, thiourea-chitosan coating on the surface of magnetite (Fe 3 O 4 ) (Ag-TCM) was successfully synthesized using Ag(I) as imprinted ions for adsorption and removal of Ag(I) ions from aqueous solutions. The thermal stability, chemical structure and magnetic property of the Ag-TCM were characterized by the scanning electron microscope (SEM), Fourier transform infrared spectrometer (FT-IR) and vibrating sample magnetometer (VSM), respectively. Batch adsorption experiments were performed to evaluate the adsorption conditions, selectivity and reusability. The results showed that the maximum adsorption capacity was 4.93 mmol/g, observed at pH 5 and temperature 30 o C. Equilibrium adsorption was achieved within 50 min. The kinetic data, obtained at the optimum pH 5, could be fitted with a pseudo-second order equation. Adsorption process could be well described by Langmuir adsorption isotherms and the maximum adsorption capacity calculated from Langmuir equation was 5.29 mmol/g. The selectivity coefficient of Ag(I) ions and other metal cations onto Ag-TCM indicated an overall preference for Ag(I) ions, which was much higher than non-imprinted thiourea-chitosan beads. Moreover, the sorbent was stable and easily recovered, the adsorption capacity was about 90% of the initial saturation adsorption capacity after being used five times.

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 ...

One-pot synthesis and transfer of PMMA/Ag photonic nanocomposites by pulsed laser deposition

Science.gov (United States)

Karoutsos, V.; Koutselas, I.; Orfanou, P.; Mpatzaka, Th.; Vasileiadis, M.; Vassilakopoulou, A.; Vainos, N. A.; Perrone, A.

2015-08-01

Nanocomposite films comprising metallic nanoparticles in polymer matrices find increasing use in emerging photonic, electronic and microsystem applications owing to their tailored advanced functionalities. The versatile development of such films based on poly-methyl-methacrylate (PMMA) matrix having embedded Ag nanoparticles is addressed here. Two low-cost one-pot chemical methods for the synthesis of bulk target nanocomposite materials are demonstrated. These nanocomposites are subsequently transferred via pulsed laser deposition using 193 nm ArF excimer laser radiation, producing films maintaining the structural and functional properties. Both target- and laser-deposited materials have been thoroughly characterized using microscopic, spectroscopic and thermal analysis methods. Infrared spectra demonstrated the close molecular PMMA chain similarity for both target and film materials, though structural alterations identified by thermal analysis proved the enhanced characteristics of films grown. High-resolution electron microscopy proved the transfer of Ag nanoparticles sized 10-50 nm. Visible absorption peaked in the spectral range of 430-440 nm and attributed to the Ag nanocomposite plasmonic response verifying the transfer of the functional performance from target to film.

Removal of I by adsorption with AgX (Ag-impregnated X Zeolite) from high-radioactive seawater waste

Energy Technology Data Exchange (ETDEWEB)

Lee, Eil Hee; Lee, Keun Young; Kim, Kwang Wook; Kim, Hyung Ju; Kim, Ik Soo; Chung, Dong Yong; Moon, Jei Kwon; Choi, Jong Won [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2016-09-15

This study aimed to the adsorption-removal of high- radioactive iodide (I) contained in the initially generated high-radioactive seawater waste (HSW), with the use of AgX (Ag-impregnated X zeolite). Adsorption of I by AgX (hereafter denoted as AgX-I adsorption) was increased by increasing the Ag-impregnated concentration in AgX, and its concentration was suitable at about 30 wt%. Because of AgCl precipitation by chloride ions contained in seawater waste, the leaching yields of Ag from AgX (Ag-impregnated concentration : about 30-35 wt%) was less than those in distilled water (< 1 mg/L). AgX-I adsorption was above 99% in the initial iodide concentration (Ci) of 0.01-10 mg/L at m/V (ratio of weight of adsorbent to solution volume)=2.5 g/L. This shows that efficient removal of I is possible. AgX-I adsorption was found to be more effective in distilled water than in seawater waste, and the influence of solution temperature was insignificant. Ag-I adsorption was better described by a Freundlich isotherm rather than a Langmuir isotherm. AgX-I adsorption kinetics can be expressed by a pseudo-second order rate equation. The adsorption rate constants (k2) decreased by increasing Ci, and conversely increased by increasing the ratio of m/V and the solution temperature. This time, the activation energy of AgX-I adsorption was about 6.3 kJ/mol. This suggests that AgX-I adsorption is dominated by physical adsorption with weaker bonds. The evaluation of thermodynamic parameters (a negative Gibbs free energy and a positive Enthalpy) indicates that AgX-I adsorption is a spontaneous reaction (forward reaction), and an endothermic reaction indicating that higher temperatures are favored.

Highly efficient degradation of thidiazuron with Ag/AgCl- activated carbon composites under LED light irradiation

Energy Technology Data Exchange (ETDEWEB)

Yang, Yisi [College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha 410128 (China); Hubei Key Laboratory for Processing and Application of Catalytic Materials, Huanggang Normal University, Huanggang 438000 (China); College of Chemical Engineering, Huanggang Normal University, Huanggang 438000 (China); Zhang, Yan [Hubei Key Laboratory for Processing and Application of Catalytic Materials, Huanggang Normal University, Huanggang 438000 (China); College of Chemical Engineering, Huanggang Normal University, Huanggang 438000 (China); Dong, Mingguang; Yan, Ting; Zhang, Maosheng [College of Chemical Engineering, Huanggang Normal University, Huanggang 438000 (China); Zeng, Qingru, E-mail: 40083763@qq.com [College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha 410128 (China)

2017-08-05

Highlights: • Photocatalytic degradation of thidiazuron was performed in a neutral water matrix. • This was carried out in the presence of Ag/AgCl-activated carbon composites and LED light. • The pH effect and the dominant active species were explored. • Degradation products and pathways in water were studied for the first time. - Abstract: Thidiazuron (TDZ; 1-phenyl-3-(1,2,3-thiadiazol-5-yl)urea) is one of the most widely used defoliant and easy to dissolve in surface water. Risk associated with the pesticide is not clearly defined, so it is important to remove/degrade TDZ with an efficient and environment friendly technology. Here, we investigated the use of Ag/AgCl-activated carbon (Ag/AgCl–AC) composites in photocatalytic degradation of TDZ under LED light. By the synergic effect of Ag/AgCl and AC, the optimum Ag/carbon weight ratio of 2:1 exhibited superior visible-light photocatalytic activity, the highest removal efficiency was close to 91% in pH 7 matrix. Different types of Ag/AgCl–AC composites were tested, all showed much faster photodegradation kinetics than bare Ag/AgCl in 210 min. The degradation products as identified by HPLC–MS revealed that the hydroxylation by hydroxyl radicals and that of oxidation by superoxide radicals as well as holes were the two main pathways for TDZ degradation. Results revealed that the adsorption concentrated TDZ molecules and the photocatalytically generated radicals rapidly degradated TDZ, the two contributions functioned together for removal of the pollutant from water.

Highly efficient degradation of thidiazuron with Ag/AgCl- activated carbon composites under LED light irradiation

International Nuclear Information System (INIS)

Yang, Yisi; Zhang, Yan; Dong, Mingguang; Yan, Ting; Zhang, Maosheng; Zeng, Qingru

2017-01-01

Highlights: • Photocatalytic degradation of thidiazuron was performed in a neutral water matrix. • This was carried out in the presence of Ag/AgCl-activated carbon composites and LED light. • The pH effect and the dominant active species were explored. • Degradation products and pathways in water were studied for the first time. - Abstract: Thidiazuron (TDZ; 1-phenyl-3-(1,2,3-thiadiazol-5-yl)urea) is one of the most widely used defoliant and easy to dissolve in surface water. Risk associated with the pesticide is not clearly defined, so it is important to remove/degrade TDZ with an efficient and environment friendly technology. Here, we investigated the use of Ag/AgCl-activated carbon (Ag/AgCl–AC) composites in photocatalytic degradation of TDZ under LED light. By the synergic effect of Ag/AgCl and AC, the optimum Ag/carbon weight ratio of 2:1 exhibited superior visible-light photocatalytic activity, the highest removal efficiency was close to 91% in pH 7 matrix. Different types of Ag/AgCl–AC composites were tested, all showed much faster photodegradation kinetics than bare Ag/AgCl in 210 min. The degradation products as identified by HPLC–MS revealed that the hydroxylation by hydroxyl radicals and that of oxidation by superoxide radicals as well as holes were the two main pathways for TDZ degradation. Results revealed that the adsorption concentrated TDZ molecules and the photocatalytically generated radicals rapidly degradated TDZ, the two contributions functioned together for removal of the pollutant from water.

Microwave assisted facile synthesis of reduced graphene oxide-silver (RGO-Ag) nanocomposite and their application as active SERS substrate

Energy Technology Data Exchange (ETDEWEB)

Wadhwa, Heena, E-mail: heenawadhwa1988@gmail.com; Kumar, Devender, E-mail: devkumsaroha@kuk.ac.in; Mahendia, Suman, E-mail: mahendia@gmail.com; Kumar, Shyam, E-mail: profshyam@gmail.com

2017-06-15

The present paper represents the facile and rapid synthesis of reduced graphene oxide-silver (RGO-Ag) nanocomposite with the help of microwave irradiation. The graphene oxide (GO) solution has been prepared in bulk using Hummer's method followed by microwave assisted in-situ reduction of GO and silver nitrate (AgNO{sub 3}) by hydrazine hydrate in a short spam of 5 min. The prepared nanocomposite has been characterized using Transmission Electron Microscopy (TEM), X-Ray Diffraction (XRD) Scanning Electron Microscopy (SEM) and UV–Visible spectroscopy. TEM analysis shows that Ag nanoparticles with average size 32 nm are uniformly entangled with in RGO layers. The UV–Visible absorption spectrum of nanocomposite depicts the reduction of GO to RGO along with the formation of Ag nanoparticles with the presence of characteristic surface Plasmon resonance (SPR) peak of Ag nanoparticles at 422 nm. The performance of prepared nanocomposite has been tested as the active Surface Enhanced Raman Scattering (SERS) substrate for Rhodamine 6G with detection limit 0.1 μM. - Highlights: • The RGO and RGO-Ag nanocomposite were synthesized with microwave irradiation. • Ag nanoparticles of average size 32 nm are uniformly entangled within RGO layers. • RGO itself is a florescence quencher with SERS detection limit 1 μM for R6G. • RGO-Ag nanocomposite show good SERS activity for R6G with detection limit 0.1 μM.

Generation of Localized Surface Plasmon Resonance Using Hybrid Au–Ag Nanoparticle Arrays as a Sensor of Polychlorinated Biphenyls Detection

Directory of Open Access Journals (Sweden)

Jing Liu

2016-08-01

Full Text Available In this study, the hybrid Au–Ag hexagonal lattice of triangular and square lattice of quadrate periodic nanoparticle arrays (PNAs were designed to investigate their extinction spectra of the localized surface plasmon resonances (LSPRs. First, their simulating extinction spectra were calculated by discrete dipole approximation (DDA numerical method by changing the media refractive index. Simulation results showed that as the media refractive index was changed from 1.0 to 1.2, the maximum peak intensity of LSPRs spectra had no apparent change and the wavelength to reveal the maximum peak intensity of LSPRs spectra was shifted lower value. Polystyrene (PS nanospheres with two differently arranged structures were used as the templates to deposit the hybrid Au–Ag hexagonal lattice of triangular and square lattice of quadrate periodic PNAs by evaporation method. The hybrid Au–Ag hexagonal lattice of triangular and square lattice of quadrate PNAs were grown on single crystal silicon (c-Si substrates, and their measured extinction spectra were compared with the calculated results. Finally, the fabricated hexagonal lattices of triangular PNAs were investigated as a sensor of polychlorinated biphenyl solution (PCB-77 by observing the wavelength to reveal the maximum extinction efficiency (λmax. We show that the adhesion of β-cyclodextrins (SH-β-CD on the hybrid Au–Ag hexagonal lattice of triangular PNAs could be used to increase the variation of λmax. We also demonstrate that the adhesion of SH-β-CD increases the sensitivity and detection effect of PCB-77 in hexagonal lattice of triangular PNAs.

Ag/AgCl Loaded Bi2WO6 Composite: A Plasmonic Z-Scheme Visible Light-Responsive Photocatalyst

Directory of Open Access Journals (Sweden)

Xiangchao Meng

2016-01-01

Full Text Available Hierarchical flower-like Bi2WO6 was successfully synthesized by facile hydrothermal method at low pH. And Ag/AgCl was loaded by photoreduction on its surface. As-prepared photocatalysts were characterized by various techniques. Bi2WO6 was successfully synthesized at a size of 2-3 μm. Depositing Ag/AgCl did not destroy the crystal structure, and both Ag+ and metallic Ag0 were found. The band gap of the composite was 2.57 eV, which indicates that visible light could be the activating irradiation. In the photocatalytic activity test, the composite with 10 wt% Ag/AgCl boasted the highest removal efficiency (almost 100% in 45 min. The significant enhancement can be attributed to the surface plasmon resonance (SPR effect and the establishment of heterostructures between Ag/AgCl and Bi2WO6. A possible mechanism of photocatalytic oxidation in the presence of Ag/AgCl-Bi2WO6 was proposed. This work sheds light on the potential applications of plasmonic metals in photocatalysis to enhance their activities.

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

Directory of Open Access Journals (Sweden)

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.

In situ thermal residual stress evolution in ultrathin ZnO and Ag films studied by synchrotron x-ray diffraction

Energy Technology Data Exchange (ETDEWEB)

Renault, P.O., E-mail: Pierre.olivier.renault@univ-poitiers.fr [Institut P' , CNRS, Universite de Poitiers, UPR 3346, 86962 Futuroscope (France); Krauss, C.; Le Bourhis, E.; Geandier, G. [Institut P' , CNRS, Universite de Poitiers, UPR 3346, 86962 Futuroscope (France); Benedetto, A. [Saint-Gobain Recherche (SGR), 93303 Aubervilliers (France); Grachev, S.Y.; Barthel, E. [Lab. Surface du Verre et Interfaces (SVI), UMR-CNRS 125, 93303 Aubervilliers (France)

2011-12-30

Residual-stress evolution in sputtered encapsulated ZnO/Ag/ZnO stack has been studied in-situ by synchrotron x-ray diffraction when heat treated. The ZnO/Ag/ZnO stack encapsulated into Si{sub 3}N{sub 4} layers and deposited on (001) Si substrates was thermally heated from 25 Degree-Sign C to 600 Degree-Sign C and cooled down to 25 Degree-Sign C. X-ray diffraction 2D patterns captured continuously during the heat treatment allowed monitoring the diffraction peak shifts of both Ag (15 nm thick) and ZnO (10 nm and 50 nm thick) sublayers. Due to the mismatch between the coefficients of thermal expansion, the silicon substrate induced compressive thermal stresses in the films during heating. We first observed a linear increase of the compressive stress state in both Ag and ZnO films and then a more complex elastic-stress evolution starts to operate from about 100 Degree-Sign C for Ag and about 250 Degree-Sign C for ZnO. Thermal contraction upon cooling seems to dominate so that the initial compressive film stresses relax by about 300 and 700 MPa after thermal treatment for ZnO and Ag, respectively. The overall behavior is discussed in terms of structural changes induced by the heat treatment.

A Study on the Significance of the Colloidal Radiogold Disappearance Rate as a Simple Clinical Liver Function Test

International Nuclear Information System (INIS)

Hong, Chang Gi

1969-01-01

Liver function in diffuse parenchymal liver such as cirrhosis of the liver depend largely on the effective hepatic blood flow rather than on the individual cell functions. Clinical methods of measuring the hepatic blood flow were developed recently by the application of colloidal disappearance rate. In order to correlate the radiogold disappearance rate to conventional biochemical liver function tests, 21 normal subjects and 80 cases of cirrhosis of the liver were studied with both methods. The results are summarized as following: 1) The validity of external counting method to measure the blood disappearance rate of colloidal radiogold was confirmed by in vitro counting of the serial blood samples. 2) The blood disappearance rate of colloidal radiogold was essentially the same as the liver uptake rate of colloidal radiogold in normal and cirrhotic subjects with various degrees of functional disturbance. And it seemed there was no serious extrahepatic removal of the colloidal radiogold. 3) The disappearance rate of colloidal radiogold was not significant changed by the posture change, but was enhanced by ingestion of 500 ml of water. 4) The disappearance rate of colloidal radiogold was not influenced y single dose of Telepaque, while BSP retention was increased after Telepaque. 5) The mean disappearance half time of colloidal radiogold in normal subjects was 2.49±0.391 (S.D.) minutes. The mean normal disappearance rate constant (K value) was 0.285±0.0428 (S.D.)/minute. 6) The colloidal radiogold disappearance half time was abnormally prolonged (over 3.2 mm) in 87.7±3.68 (S.D.) % of cirrhotic subjects. 7) In patients of liver cirrhosis the blood disappearance rate of colloidal radiogold correlated well to serum albumin and globulin levels and BSP retention which were considered to reflect functions of hepatic parenchymal cells. There was, however, no correlation between colloidal disappearance rate and thymol turbidity test, serum glutamic pyruvic transaminase

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

Effects of a Thin Ru-Doped PVP Interface Layer on Electrical Behavior of Ag/n-Si Structures

Science.gov (United States)

Badali, Yosef; Nikravan, Afsoun; Altındal, Şemsettin; Uslu, İbrahim

2018-03-01

The aim of this study is to improve the electrical property of Ag/n-Si metal-semiconductor (MS) structure by growing an Ru-doped PVP interlayer between Ag and n-Si using electrospinning technique. To illustrate the utility of the Ru-doped PVP interface layer, current-voltage (I-V) characteristics of Ag/n-Si (MS) and Ag/Ru-doped PVP/n-Si metal-polymer-semiconductor (MPS) structures was carried out. In addition, the main electrical parameters of the fabricated Ag/Ru-doped PVP/n-Si structures were investigated as a function of frequency and electric field using impedance spectroscopy method (ISM). The capacitance-voltage (C-V) plot showed an anomalous peak in the depletion region due to the special density distribution of interface traps/states (D it /N ss) and interlayer. Both the values of series resistance (R s) and N ss were drawn as a function of voltage and frequency between 0.5 kHz and 5 MHz at room temperature and they had a peak behavior in the depletion region. Some important parameters of the sample such as the donor concentration atoms (N D), Fermi energy (E F ), thickness of the depletion region (W D), barrier height (Φ B0 ) and R s were determined from the C -2 versus V plot for each frequency. The values of N D , W D , Φ B0 and R s were changed from 1 × 1015 cm-3, 9.61 × 10-5 cm, 0.94 eV and 19,055 Ω (at 0.5 kHz) to 0.13 × 1015 cm-3, 27.4 × 10-4 cm, 1.04 eV and 70 Ω (at 5 MHz), respectively. As a result of the experiments, it is observed that the change in electrical parameters becomes more effective at lower frequencies due to the N ss and their relaxation time (τ), dipole and surface polarizations.

Pulmonary deposition and disappearance of aerosolised secretory leucocyte protease inhibitor.

Science.gov (United States)

Stolk, J.; Camps, J.; Feitsma, H. I.; Hermans, J.; Dijkman, J. H.; Pauwels, E. K.

1995-01-01

BACKGROUND--The neutrophil elastase inhibitor, secretory leucocyte protease inhibitor (SLPI), is a potential therapeutic tool in inflammatory lung diseases such as cystic fibrosis and pulmonary emphysema. The distribution and disappearance in the lung of aerosolised recombinant SLPI (rSLPI) was investigated in healthy humans and in patients with cystic fibrosis or alpha 1-antitrypsin-associated emphysema. METHODS--To distinguish aerosolised rSLPI from endogenous SLPI the recombinant inhibitor was radiolabelled with 99m-technetium (99mTc) pertechnetate. Distribution and disappearance of aerosolised 99mTc-rSLPI in the lungs were studied by gamma radiation imaging. RESULTS--The deposition of 99mTc-rSLPI in normal volunteers was homogeneous in all lung lobes, while in patients with cystic fibrosis or emphysema only well ventilated areas showed deposition of the aerosol. The disappearance rate of 99mTc-rSLPI was biexponential. The half life of the rapid phase was 0.2-2.8 hours, while that of the slow phase was more than 24 hours. CONCLUSIONS--Future aerosol therapy with rSLPI will be most beneficial for well ventilated lung tissue that needs protection against neutrophil derived elastase. It may be more difficult to neutralise the burden of elastase in poorly ventilated, highly inflamed areas as are seen in cystic fibrosis. Images PMID:7638807

Rapid Biosynthesis of AgNPs Using Soil Bacterium Azotobacter vinelandii With Promising Antioxidant and Antibacterial Activities for Biomedical Applications

Science.gov (United States)

Karunakaran, Gopalu; Jagathambal, Matheswaran; Gusev, Alexander; Torres, Juan Antonio Lopez; Kolesnikov, Evgeny; Kuznetsov, Denis

2017-07-01

Silver nanoparticles (AgNPs) are applied in various fields from electronics to biomedical applications as a result of their high surface-to-volume ratio. Even though different approaches are available for synthesis of AgNPs, a nontoxic method for the synthesis has not yet been developed. Thus, this study focused on developing an easy and ecofriendly approach to synthesize AgNPs using Azotobacter vinelandii culture extracts. The biosynthesized nanoparticles were further characterized by ultraviolet-visible (UV-Vis) spectroscopy, x-ray diffraction (XRD), Fourier transform infrared (FTIR), energy-dispersive spectrum, particle size distribution (PSD), and transmission electron microscopy (TEM). UV absorption noticed at 435 nm showed formation of AgNPs. The XRD pattern showed a face-centered cubic structure with broad peaks of 28.2°, 32.6°, 46.6°, 55.2°, 57.9°, and 67.8°. The FTIR confirmed the involvement of various functional groups in the biosynthesis of AgNPs. The PSD and TEM analyses showed spherical, well-distributed nanoparticles with an average size of 20-70 nm. The elemental studies confirmed the existence of pure AgNPs. The bacterial extract containing extracellular enzyme nitrate reductase converted silver nitrate into AgNPs. AgNPs significantly inhibited the growth of pathogenic bacteria such as Streptomyces fradiae (National Collection of Industrial Microorganisms (NCIM) 2419), Staphylococcus aureus (NCIM 2127), Escherichia coli (NCIM 2065), and Serratia marcescens (NCIM 2919). In addition, biosynthesized AgNPs were found to possess strong antioxidant activity. Thus, the results of this study revealed that biosynthesized AgNPs could serve as a lead in the development of nanomedicine.

The Effect of Ag and Ag+N Ion Implantation on Cell Attachment Properties

International Nuclear Information System (INIS)

Urkac, Emel Sokullu; Oztarhan, Ahmet; Gurhan, Ismet Deliloglu; Iz, Sultan Gulce; Tihminlioglu, Funda; Oks, Efim; Nikolaev, Alexey; Ila, Daryush

2009-01-01

Implanted biomedical prosthetic devices are intended to perform safely, reliably and effectively in the human body thus the materials used for orthopedic devices should have good biocompatibility. Ultra High Molecular Weight Poly Ethylene (UHMWPE) has been commonly used for total hip joint replacement because of its very good properties. In this work, UHMWPE samples were Ag and Ag+N ion implanted by using the Metal-Vapor Vacuum Arc (MEVVA) ion implantation technique. Samples were implanted with a fluency of 1017 ion/cm2 and extraction voltage of 30 kV. Rutherford Backscattering Spectrometry (RBS) was used for surface studies. RBS showed the presence of Ag and N on the surface. Cell attachment properties investigated with model cell lines (L929 mouse fibroblasts) to demonstrate that the effect of Ag and Ag+N ion implantation can favorably influence the surface of UHMWPE for biomedical applications. Scanning electron microscopy (SEM) was used to demonstrate the cell attachment on the surface. Study has shown that Ag+N ion implantation represents more effective cell attachment properties on the UHMWPE surfaces.

Chromatographic analysis of phytochemicals components present in mangifera indica leaves for the synthesis of silver nanoparticles by AgNO3 reduction

Science.gov (United States)

Martínez-Bernett, D.; Silva-Granados, A.; Correa-Torres, S. N.; Herrera, A.

2016-02-01

It was studied the green synthesis of silver nanoparticles (AgNPs) from the reduction of a silver nitrate solution (1 and 10mM) in the presence of an extract of mangifera indica leaves. Phytochemicals components present in extracts of mango leaves were determined using a GC-MS chromatograph. The results showed the presence of the phenolic compound pyrogallol (26.9% wt/5mL of extract) and oleic acid (29.1% wt/5mL of extract), which are useful for the reduction of the metallic salt AgNO3 and the stabilization of silver nanoparticles. The synthesized nanoparticles were characterized by UV visible spectroscopy (UV-vis), evidencing absorbances at wavelengths of 417nm (AgNPs-1) and 414nm (AgNPs- 10), which are characteristic peaks of this metallic nanoparticles. Scanning Electron Microscopy (SEM) was used to determine the size of the synthesized nanoparticles. A particle size of about 28±7nm was observed for the AgNPs-1 sample and 26±5nm for the AgNPs-10. This suggests the advantages of green chemistry to obtain silver nanoparticles with a narrow size distribution.

Chromatographic analysis of phytochemicals components present in mangifera indica leaves for the synthesis of silver nanoparticles by AgNO3 reduction

International Nuclear Information System (INIS)

Martínez-Bernett, D; Silva-Granados, A; Herrera, A; Correa-Torres, S N

2016-01-01

It was studied the green synthesis of silver nanoparticles (AgNPs) from the reduction of a silver nitrate solution (1 and 10mM) in the presence of an extract of mangifera indica leaves. Phytochemicals components present in extracts of mango leaves were determined using a GC-MS chromatograph. The results showed the presence of the phenolic compound pyrogallol (26.9% wt/5mL of extract) and oleic acid (29.1% wt/5mL of extract), which are useful for the reduction of the metallic salt AgNO 3 and the stabilization of silver nanoparticles. The synthesized nanoparticles were characterized by UV visible spectroscopy (UV-vis), evidencing absorbances at wavelengths of 417nm (AgNPs-1) and 414nm (AgNPs- 10), which are characteristic peaks of this metallic nanoparticles. Scanning Electron Microscopy (SEM) was used to determine the size of the synthesized nanoparticles. A particle size of about 28±7nm was observed for the AgNPs-1 sample and 26±5nm for the AgNPs-10. This suggests the advantages of green chemistry to obtain silver nanoparticles with a narrow size distribution. (paper)

Improved Catalysis of Green-Synthesized Pd-Ag Alloy-Nanoparticles for Anodic Oxidation of Methanol in Alkali

International Nuclear Information System (INIS)

Roy Chowdhury, Sreya; Ghosh, Srabanti; Bhattachrya, Swapan Kumar

2017-01-01

Highlights: • Pd and Pd x Ag y nanoalloys are synthesised by simple green synthetic method without using any capping agent. • Increased electrochemical surface area and roughness factor in case of Pd x Ag y alloy generates enhanced catalytically active sites which help methanol oxidation reaction. • By analysing the products of MOR reaction by CV, FTIR and HPLC plausible mechanism of the reaction is proposed. • Among different compositions Pd 4 Ag and Pd are the best electrodes for oxidation of methanol and formate respectively in alkali. - Abstract: Monometallic Pd, Ag and bimetallic Pd x Ag y alloy nanoparticles were synthesized in a single pot using a green synthetic protocol in absence of any capping agent. X-ray, electron diffraction, microscopic and spectroscopic studies of synthesized material demonstrate the formation of nanoballs with radius of 10–20 nm of face centred cubic metals and alloys. The electrochemical studies of as-synthesized materials loaded on carbon support reveal that the Pd 4 Ag nanoparticles exhibit the best and synergistic electro-catalytic activity in reference to oxidation of methanol in alkali. The most active Pd 4 Ag nanoparticles show higher peak current (201 mA mg −1 ) in comparison to that (133 mA mg −1 ) of Pd in cyclic voltammetric study. The electrode shows the highest exchange current density (1.95 × 10 −2 mA mg −1 of Pd) for methanol oxidation reaction (MOR) and higher catalytic activity for oxidation of possible intermediates like formaldehyde and sodium formate of MOR. Ex-situ infrared spectrometry and chromatographic studies of reaction products reveal that Ag accelerates the formation of formate rather than carbonate elucidating the plausible mechanism of the reaction. These findings have important implications for further fine-tuning of the Pd nano alloys toward highly active and selective catalysts for alcohol fuel cells.

Green synthesis of graphene/Ag nanocomposites

International Nuclear Information System (INIS)

Yuan Wenhui; Gu Yejian; Li Li

2012-01-01

Graphical abstract: A facile and green approach to synthesis of GNS/AgNPs is reported by employing sodium citrate as reductant, and this study represents the use of biocompounds for nontoxic and scalable production of GNS/AgNPs under a suitable concentration of silver ions and the prepared GNS/AgNPs can be used in the field of disinfection. Highlights: ► Graphene/Ag nanocomposites were prepared by a green and facile strategy based on sodium citrate. ► The influence of AgNO 3 amount on particle size and size range of AgNPs was studied. ► The surface plasmon resonance properties of AgNPs on graphene was investigated. ► The antibacterial activity of silver nanoparticles was retained in the nanocomposites. - Abstract: Graphene/Ag nanocomposites (GNS/AgNPs) were fabricated via a green and facile method, employing graphite oxide (GO) as a precursor of graphene, AgNO 3 as a precursor of Ag nanoparticles, and sodium citrate as an environmentally friendly reducing and stabilizing agent. The synthesized GNS/AgNPs were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS) and Raman spectra (RS), respectively. The results indicated that graphite oxide was completely reduced to graphene, and the silver ion was reduced by sodium citrate simultaneously. Under a suitable dosage of silver ions, well-dispersed AgNPs on the graphene sheets mostly centralized at 20–25 nm. The surface plasmon resonance property of AgNPs on graphene showed that there was a interaction between AgNPs and graphene supports. In addition, antibacterial activity of silver nanoparticles was retained in the nanocomposites, suggesting that they can be potentially used as a graphene-based biomaterial.

Preparation of ultra-thin polypyrrole nanosheets decorated with Ag nanoparticles and their application in hydrogen peroxide detection

International Nuclear Information System (INIS)

Mahmoudian, M.R.; Alias, Y.; Basirun, W.J.; Ebadi, M.

2012-01-01

Highlights: ► Ag nanoparticles-decorated ultra thin polypyrrole nanosheets were prepared. ► Higher surface area of the polymer increased interaction between the polymer and Ag + . ► The sensitivity was estimated to be 4.477 μA mM −1 for linear segment. ► The LOD and LOQ (S/N = 3) were estimated to be 0.57 μM and 1.93 μM, respectively. - Abstract: This study examines the preparation of ultra-thin polypyrrole nanosheets decorated with Ag nanoparticles (Ag-UTPNSs) and their application in the enzyme-less detection of hydrogen peroxide (H 2 O 2 ) detection. The X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM) results confirmed that Ag nanoparticles (NPs) were deposited onto the surface of the UTPNSs. The increase of the H 2 O 2 reduction current peak to 120 μA in the presence of the Ag-UTPNS/glassy carbon electrode (GCE) as compared to the UTPNS/GCE indicates that the sensitivity of the electrode to H 2 O 2 is significant. This observation can be explained by the larger surface area of the UTPNSs, which can increase the interactions between the polymer and the AgNO 3 solution during the deposition of the Ag NPs, and by the small size of the deposited Ag NPs, which can produce a surface area of Ag that is suitable for the reaction with H 2 O 2 . The amperometric responses show that the limit of detection, the limit of quantification (S/N = 3) and the sensitivity are estimated to be 0.57 μM, 1.93 μM and 4.477 μA mM −1 , respectively, for the linear segment. The results of the reproducibility experiments show that the use of Ag-UTPNS/GCE is feasible for the quantitative detection of certain concentration ranges of H 2 O 2 .

CO oxidation catalyzed by ag nanoparticles supported on SnO/CeO2

KAUST Repository

Khan, Inayatali

2015-01-01

Ag-Sn/CeO2 catalysts were synthesized by the co-precipitation method with different Ag-Sn wt.% loadings and were tested for the oxidation of CO. The catalysts were characterized by powder X-ray diffractometry (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), energy dispersive X-ray spectroscopy (EDS), and selected area electron diffraction (SAED) techniques. UV-Vis measurements were carried out to elucidate the ionic states of the silver particles, and the temperature-programmed reduction (TPR) technique was employed to check the reduction temperature of the catalyst supported on CeO2. There are peaks for silver crystallites in the X-ray diffraction patterns and the presence of SnO was not well evidenced by the XRD technique due to sintering inside the 3D array channels of CeO2 during the calcination process. The Ag-Sn/CeO2 (4%) catalyst was the most efficient and exhibited 100% CO oxidation at 100 °C due to small particle size and strong electronic interaction with the SnO/CeO2 support. © 2015 Sociedade Brasileira de Química.

Improvement of photocatalytic activities of Ag/P25 hybrid systems by controlled morphology of Ag nanoprisms

Energy Technology Data Exchange (ETDEWEB)

Lee, Ti, E-mail: r01527017@ntu.edu.tw [Department of Materials Science and Engineering, National Taiwan University, Taipei 10617, Taiwan (China); Chao, Bo-Kai, E-mail: d98527007@ntu.edu.tw [Department of Materials Science and Engineering, National Taiwan University, Taipei 10617, Taiwan (China); Kuo, Yu-Lin, E-mail: ylkuo@mail.ntust.edu.tw [Department of Mechanical Engineering, National Taiwan University of Science and Technology, Taipei 10607, Taiwan (China); Hsueh, Chun-Hway, E-mail: hsuehc@ntu.edu.tw [Department of Materials Science and Engineering, National Taiwan University, Taipei 10617, Taiwan (China)

2017-05-01

Constructing hybrid systems with noble metal nanostructures is one known way to improve the poor photocatalysis efficiency of TiO{sub 2} under visible light. In our study, two different Ag nanostructures were prepared: (1) Ag nanospheres synthesized by chemical reduction method, and (2) Ag nanoprisms transformed from nanospheres with an additional photo-conversion process. Both Ag-TiO{sub 2} hybrid systems were prepared by mixing various concentrations of Ag solutions with commercial TiO{sub 2} powder (P25), and they were then utilized as photocatalysts for the photodecolorization test of methyl blue under various light sources (fluorescent, UV light and red LED lamps) irradiations. Results of the photodecolorization tests showed that Ag nanostructures could evidently enhance the photocatalytic activity of TiO{sub 2} under different light sources, while an optimal composition of 0.432 wt% Ag nanoprisms/TiO{sub 2} displayed superior photocatalytic properties under visible light irradiations (fluorescent and red LED lamps). The enhanced photocatalytic activities could be mainly attributed to the mechanisms of hot electrons injection and resonant energy transfer by the localized surface plasmon resonance of Ag nanostructures and the electronic states favorable of charge separation at the interface between metals and semiconductors. - Highlights: • We used Ag nanostructures to improve photocatalysis efficiency of TiO{sub 2}. • Ag nanoprisms were more efficient than Ag nanospheres under visible light. • Ag nanoprisms/P25 is about 7 times more efficient than P25 under fluorescent lamp. • Mechanisms rely on hot electrons injection and resonant energy transfer by LSPR.

Improvement of photocatalytic activities of Ag/P25 hybrid systems by controlled morphology of Ag nanoprisms

International Nuclear Information System (INIS)

Lee, Ti; Chao, Bo-Kai; Kuo, Yu-Lin; Hsueh, Chun-Hway

2017-01-01

Constructing hybrid systems with noble metal nanostructures is one known way to improve the poor photocatalysis efficiency of TiO_2 under visible light. In our study, two different Ag nanostructures were prepared: (1) Ag nanospheres synthesized by chemical reduction method, and (2) Ag nanoprisms transformed from nanospheres with an additional photo-conversion process. Both Ag-TiO_2 hybrid systems were prepared by mixing various concentrations of Ag solutions with commercial TiO_2 powder (P25), and they were then utilized as photocatalysts for the photodecolorization test of methyl blue under various light sources (fluorescent, UV light and red LED lamps) irradiations. Results of the photodecolorization tests showed that Ag nanostructures could evidently enhance the photocatalytic activity of TiO_2 under different light sources, while an optimal composition of 0.432 wt% Ag nanoprisms/TiO_2 displayed superior photocatalytic properties under visible light irradiations (fluorescent and red LED lamps). The enhanced photocatalytic activities could be mainly attributed to the mechanisms of hot electrons injection and resonant energy transfer by the localized surface plasmon resonance of Ag nanostructures and the electronic states favorable of charge separation at the interface between metals and semiconductors. - Highlights: • We used Ag nanostructures to improve photocatalysis efficiency of TiO_2. • Ag nanoprisms were more efficient than Ag nanospheres under visible light. • Ag nanoprisms/P25 is about 7 times more efficient than P25 under fluorescent lamp. • Mechanisms rely on hot electrons injection and resonant energy transfer by LSPR.

Ozone decomposition on Ag/SiO2 and Ag/clinoptilolite catalysts at ambient temperature

International Nuclear Information System (INIS)

Nikolov, Penko; Genov, Krassimir; Konova, Petya; Milenova, Katya; Batakliev, Todor; Georgiev, Vladimir; Kumar, Narendra; Sarker, Dipak K.; Pishev, Dimitar; Rakovsky, Slavcho

2010-01-01

Silver modified zeolite (Bulgarian natural clinoptilolite) and Ag/silica catalysts were synthesized by ion exchange and incipient wet impregnation method respectively and characterized by different techniques. DC arc-AES was used for Ag detection. XRD spectra show that Ag is loaded over the surface of the SiO 2 sample and that after the ion-exchange process the HEU type structure of clinoptilolite is retained. UV-VIS (specific reflection at 310 nm) and IR (band at 695 cm -1 ) spectroscopy analysis proved that silver is loaded as a T-atom into zeolite channels as Ag + , instead of Na + , Ca 2+ , or K + ions, existing in the natural clinoptilolite form. The samples Ag/SiO 2 and Ag-clinoptilolite were tested as catalysts for decomposition of gas phase ozone. Very high catalytic activity (up to 99%) was observed and at the same time the catalysts remained active over time at room temperature.

Using Ag/Ag2O/SnO2 Nanocomposites to Remove Malachite Green by a Photocatalytic Process

Science.gov (United States)

Taufik, A.; Paramarta, V.; Prakoso, S. P.; Saleh, R.

2017-03-01

Silver/silver oxide/tin oxide nanocomposites of various weight ratios were synthesized using a microwave-assisted method. The Ag/Ag2O:SnO2 nanoparticle weight ratios used were 25:75, 50:50, and 75:25. All samples were characterized using X-ray diffraction, UV-Vis spectroscopy, Differential Scanning Calorimetry and Thermogravimetric Analysis (TGA). The Ag/Ag2O/SnO2 nanocomposites contained cubic structures provided by the Ag and Ag2O and tetragonal structures provided by the SnO2. The silver resulted in surface plasmon resonance (SPR) at a wavelength of about 435 nm. The silver oxide material was transformed into pure Ag at a temperature of about 370 °C The photocatalytic activity was tested on the degradation of malachite green (MG) from an aqueous solution. The results showed that Ag/Ag2O/SnO2 at a ratio of 50:50 exhibited the best photocatalytic performance for degrading MG under visible-light irradiation. The degradation of MG using Ag/Ag2O/SnO2 nanocomposites followed pseudo first-order kinetic reactions, and electron holes were found to be the main species acting on the degradation process.

Ag/α-Fe{sub 2}O{sub 3} hollow microspheres: Preparation and application for hydrogen peroxide detection

Energy Technology Data Exchange (ETDEWEB)

Kang, Xinyuan; Wu, Zhiping; Liao, Fang, E-mail: liaozhang2003@163.com; Zhang, Tingting; Guo, Tingting

2015-09-15

In this paper, we demonstrated a simple approach for preparing α-Fe{sub 2}O{sub 3} hollow spheres by mixing ferric nitrate aqueous and glucose in 180 °C. The glucose was found to act as a soft template in the process of α-Fe{sub 2}O{sub 3} hollow spheres formation. Ag/α-Fe{sub 2}O{sub 3} hollow nanocomposite was obtained under UV irradiation without additional reducing agents or initiators. Synthesized Ag/α-Fe{sub 2}O{sub 3} hollow composites exhibited remarkable catalytic performance toward H{sub 2}O{sub 2} reduction. The electrocatalytic activity mechanism of Ag/α-Fe{sub 2}O{sub 3}/GCE were discussed toward the reduction of H{sub 2}O{sub 2} in this paper. - Graphical abstract: Glucose is carbonized as carbon balls in the 180 °C hydrothermal carbonization process, which plays a role of a soft template. Carbon spherical shell is rich in many hydroxyls, which have good hydrophilicity and surface reactivity. When Fe(NO{sub 3}){sub 3} is added to the aqueous solution of Glucose, the hydrophilic -OH will adsorb Fe{sup 3+} to form coordination compound by coordination bond. α-FeOOH is formed on the surface of carbon balls by hydrothermal reaction. After calcination at 500 °C, carbon spheres react with oxygen to form carbon dioxide, which disappears in the air. Meanwhile α-FeOOH is calcined to form α-Fe{sub 2}O{sub 3} hollow spheres.

Studies on electronic structure of interfaces between Ag and gelatin for stabilization of Ag nanoparticles

International Nuclear Information System (INIS)

Tani, Tadaaki; Uchida, Takayuki

2015-01-01

Extremely high stability of Ag nanoparticles in photographic materials has forced us to study the electronic structures of the interfaces between thin layers of Ag, Au, and Pt and their surface membranes in ambient atmosphere by photoelectron yield spectroscopy in air and Kelvin probe method. Owing to the Fermi level equalization between a metal layer and a membrane coming from air, the electron transfer took place from the membrane to Pt and Au layers and from an Ag layer to the membrane, giving the reason for poor stability of Ag nanoparticles in air. The control of the Fermi level of an Ag layer with respect to that of a gelatin membrane in air could be widely made according to Nernst's equation by changing the pH and pAg values of an aqueous gelatin solution used to form the membrane, and thus available to stabilize Ag nanoparticles in a gelatin matrix. (author)

Bioethics against disappearance of a man a prism of general and criminal-law theory

Directory of Open Access Journals (Sweden)

Trajković Marko

2015-01-01

Full Text Available Bioethics, as a meeting point, engrossed with its fight against the disappearance of the man, both general and criminal-law theory. Actually, its 'care' for the man is an issue that comes before general and criminal-law theory. While the forms of disappearance of the man are very diverse and very often so refined that they cannon sometimes be recognized, the fight against the disappearance of the man must be open, clear and uncompromising. What is the role of law in this fight? The role imposed itself. Even if the law did not want to take part in the fight, it found itself in the middle of the battlefield because human life is protected from beginning to the end by legal norms that should emerge from the best writings of general and criminal-law theory. However, self-sufficiency of law and mere legal positivism are a true obstacle in this battle. This pressure and the lack of questionings are the first step on the road to disappearance of the man, because a man that asks questions is the man that exists. He and his boldness are a barrier to voluntarism. The lack of boldness of the man opens the gates to his disappearance. This boldness has not been taken away from him in the field of bioethics, which is neither secular nor religious, but rather unique as the man is unique.

Structural, optical and electrical characterization of ITO, ITO/Ag and ITO/Ni transparent conductive electrodes

International Nuclear Information System (INIS)

Ali, Ahmad Hadi; Shuhaimi, Ahmad; Hassan, Zainuriah

2014-01-01

We report on the transparent conductive oxides (TCO) characteristics based on the indium tin oxides (ITO) and ITO/metal thin layer as an electrode for optoelectronics device applications. ITO, ITO/Ag and ITO/Ni were deposited on Si and glass substrate by thermal evaporator and radio frequency (RF) magnetron sputtering at room temperature. Post deposition annealing was performed on the samples in air at moderate temperature of 500 °C and 600 °C. The structural, optical and electrical properties of the ITO and ITO/metal were characterized using X-ray diffraction (XRD), UV–Vis spectrophotometer, Hall effect measurement system and atomic force microscope (AFM). The XRD spectrum reveals significant polycrystalline peaks of ITO (2 2 2) and Ag (1 1 1) after post annealing process. The post annealing also improves the visible light transmittance and electrical resistivity of the samples. Figure of merit (FOM) of the ITO, ITO/Ag and ITO/Ni were determined as 5.5 × 10 −3 Ω −1 , 8.4 × 10 −3 Ω −1 and 3.0 × 10 −5 Ω −1 , respectively. The results show that the post annealed ITO with Ag intermediate layer improved the efficiency of the transparent conductive electrodes (TCE) as compared to the ITO and ITO/Ni.

Ruhrgas AG. Business report 2000; Ruhrgas AG. Geschaeftsbericht 2000

Energy Technology Data Exchange (ETDEWEB)

NONE

2001-07-01

A detailed account of the situation of the international gas market provides the basis of the status report of Ruhrgas AG and the group of affiliated companies. Emphasis is placed on gas procurement aspects, sales volumes, the construction and operation of natural gas distribution systems, and on development, utilization and application aspects. The activities and situation of major Ruhrgas AG holding companies are described, and the annual financial statements are documented. (orig.) [German] Ausgehend von einer eingehenden Beschreibung des internationalen Gasmarktes wird ein Lagebericht des Konzerns sowie der Ruhrgas AG gegeben. Dabei wird insbesondere auf Fragen der Gasbeschaffung, des Gasabsatzes, des Baus und Betriebs von Erdgasverteilungsnetzen, sowie der Entwicklung und der Anwendungstechnik eingegangen. Ferner wird ueber den Geschaeftsverlauf wesentlicher Ruhrgas-Beteiligungsgesellschaften berichtet. Abschliessend wird der Jahresabschluss dokumentiert. (orig.)

Multiple testing issues in discriminating compound-related peaks and chromatograms from high frequency noise, spikes and solvent-based nois in LC-MS data sets

NARCIS (Netherlands)

Nyangoma, S.O.; Van Kampen, A.A.; Reijmers, T.H.; Govorukhina, N.I; van der Zee, A.G.; Billingham, I.J; Bischoff, Rainer; Jansen, R.C.

2007-01-01

Multiple testing issues in discriminating compound-related peaks and chromatograms from high frequency noise, spikes and solvent-based noise in LC-MS data sets.Nyangoma SO, van Kampen AA, Reijmers TH, Govorukhina NI, van der Zee AG, Billingham LJ, Bischoff R, Jansen RC. University of Birmingham.

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.

Mg-controlled formation of Mg–Ag co-clusters in initial aged Al–Cu–Mg–Ag alloys

International Nuclear Information System (INIS)

Bai, Song; Liu, Zhiyi; Zhou, Xuanwei; Xia, Peng; Zeng, Sumin

2014-01-01

Highlights: • The strongest age-hardening response was found in 0.81Mg alloy. • Quantitative APT study showed strong dependence of Mg–Ag co-clustering on Mg content. • A critical Mg content related to the greatest Mg–Ag co-clustering was revealed. • The evolution from Mg–Ag co-clusters to Ω phase was accelerated in 1.18Mg alloy. - Abstract: The effect of Mg variations on the number density, solute concentrations and sizes of Mg–Ag co-clusters at the early aging stage, as well as the age-hardening response of different Al–Cu–Mg–Ag alloys, was well investigated by a combination of Vickers hardness measurement, transmission electron microscopy (TEM) and atom probe tomography (APT). The strongest age-hardening response at 165 °C was found in 0.81Mg alloy, accompanied by the highest nucleation rate of Mg–Ag co-clusters after aging for 0.5 h. However, the least response was revealed in 0.39Mg alloy. By quantitative APT analysis, the observed trend in the total number density of Mg–Ag co-clusters suggested the following order: 0.81Mg alloy > 0.39Mg alloy > 1.18Mg alloy. This parabolic change in the total number density of Mg–Ag co-clusters with increasing Mg highlighted the existence of a critical Mg content, which contributed to the greatest nucleation kinetics of Mg–Ag co-clusters. As Mg increased from 0.39 to 0.81, the formation of small Mg–Ag co-clusters was significantly promoted, whereas the number density of large Mg–Ag co-clusters almost remained constant. Moreover, the remarkable enrichment of Cu within Mg–Ag co-clusters indicated that the accelerated evolution from Mg–Ag co-clusters to Ω phase was responsible for the lowest number density of Mg–Ag co-clusters in 1.18Mg alloy after aging at 165 °C for 0.5 h

[A peak recognition algorithm designed for chromatographic peaks of transformer oil].

Science.gov (United States)

Ou, Linjun; Cao, Jian

2014-09-01

In the field of the chromatographic peak identification of the transformer oil, the traditional first-order derivative requires slope threshold to achieve peak identification. In terms of its shortcomings of low automation and easy distortion, the first-order derivative method was improved by applying the moving average iterative method and the normalized analysis techniques to identify the peaks. Accurate identification of the chromatographic peaks was realized through using multiple iterations of the moving average of signal curves and square wave curves to determine the optimal value of the normalized peak identification parameters, combined with the absolute peak retention times and peak window. The experimental results show that this algorithm can accurately identify the peaks and is not sensitive to the noise, the chromatographic peak width or the peak shape changes. It has strong adaptability to meet the on-site requirements of online monitoring devices of dissolved gases in transformer oil.

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.

AgSbSe2 and AgSb(S,Se)2 thin films for photovoltaic applications

International Nuclear Information System (INIS)

Garza, J.G.; Shaji, S.; Rodriguez, A.C.; Das Roy, T.K.; Krishnan, B.

2011-01-01

Silver antimony selenide (AgSbSe 2 ) thin films were prepared by heating sequentially deposited multilayers of antimony sulphide (Sb 2 S 3 ), silver selenide (Ag 2 Se), selenium (Se) and silver (Ag). Sb 2 S 3 thin film was prepared from a chemical bath containing SbCl 3 and Na 2 S 2 O 3 , Ag 2 Se from a solution containing AgNO 3 and Na 2 SeSO 3 and Se thin films from an acidified solution of Na 2 SeSO 3 , at room temperature on glass substrates. Ag thin film was deposited by thermal evaporation. The annealing temperature was 350 deg. C in vacuum (10 -3 Torr) for 1 h. X-ray diffraction analysis showed that the thin films formed were polycrystalline AgSbSe 2 or AgSb(S,Se) 2 depending on selenium content in the precursor films. Morphology and elemental analysis of these films were done using scanning electron microscopy and energy dispersive X-ray spectroscopy. Optical band gap was evaluated from the UV-visible absorption spectra of these films. Electrical characterizations were done using Hall effect and photocurrent measurements. A photovoltaic structure: glass/ITO/CdS/AgSbSe 2 /Al was formed, in which CdS was deposited by chemical bath deposition. J-V characteristics of this structure showed V oc = 435 mV and J sc = 0.08 mA/cm 2 under illumination using a tungsten halogen lamp. Preparation of a photovoltaic structure using AgSbSe 2 as an absorber material by a non-toxic selenization process is achieved.

Rapid Formation and Disappearance of a Filament Barb

Science.gov (United States)

Joshi, Anand D.; Srivastava, Nandita; Mathew, Shibu K.; Martin, Sara F.

2013-11-01

We present observations of an activated quiescent filament obtained in Hα from the high-resolution Dutch Open Telescope (DOT) on 20 August 2010. The filament developed a barb in 10 min, which disappeared within the next 35 min. A data set from the DOT spanning 2 h was used to analyse this event. Line-of-sight velocity maps were constructed from the Doppler images, which reveal flows in filament spine during this period. Photospheric magnetograms were used from the Helioseismic and Magnetic Imager (HMI) on board the Solar Dynamics Observatory (SDO) to determine the changes in magnetic flux in the region surrounding the barb location. The analysis shows flows in the filament spine towards the barb location preceding its formation, and flows in the barb towards the spine during its disappearance. Magnetograms reveal patches of minority polarity flux close to the end of the barb at its greatest elongation. The flows in the spine and barbs are along numerous threads that compose these typical filament structures. The flows are consistent with field-aligned threads and demonstrate that the replacement time of the mass in barbs, and by inference, in the spine is very rapid.

A research on shape-controllable synthesis of Ag3PO4/AgBr and its degradation of ciprofloxacin.

Science.gov (United States)

Chen, Jingran; Yang, Xingyu; Zhu, Chenyu; Xie, Xin; Lin, Cuiping; Zhao, Yalei; Yan, Qishe

2018-03-01

Antibiotic ciprofloxacin is one of the commonly used broad spectrum fluoroquinolone human and veterinary drugs. Because of the overuse of human beings, the presence of ciprofloxacin has been detected in a variety of environmental matrices. To solve this problem, a facile, environmentally-friendly Ag 3 PO 4 /AgBr composite photocatalyst was synthesized by a simple precipitation method at room temperature in the presence of cetyltrimethyl ammonium bromide (CTAB). CTAB was served as surfactant and the source of bromide ions. The as-prepared Ag 3 PO 4 /AgBr microspheres were characterized by means of powder X-ray diffraction (XRD), scanning electron microscope (SEM) and UV-visible diffuse reflectance spectroscopy (UV-vis DRS). The results revealed that the Ag 3 PO 4 /AgBr sample (synthesized with CTAB, 0.8 g) exhibited the highest photocatalytic activity to the photodegradation rate of 96.36%. Moreover, mechanism detection experiment indicated that h + was the major active species in the degradation process. So the enhanced photocatalytic activity of Ag 3 PO 4 /AgBr composites is attributed to its excellent separation of photogenerated electron-hole pairs through Ag 3 PO 4 /AgBr heterojunction. Also, Ag 3 PO 4 /AgBr heterojunction has a lower band gap compared to pure Ag 3 PO 4 and pure AgBr, so higher efficiency of light harvesting is equipped.

Processes of adsorption/desorption of iodides and cadmium cations onto/from Ag(111

Directory of Open Access Journals (Sweden)

VLADIMIR D. JOVIĆ

2011-02-01

Full Text Available In this work, the adsorption/desorption processes of iodides and cadmium cations in the presence of iodides onto/from Ag(111 were investigated. It was shown that both processes were complex, characterized by several peaks on the cyclic voltammograms (CVs. By PeakFit analysis of the recorded CVs and subsequent fitting of the obtained peaks by the Frumkin adsorption isotherm, the interaction parameter (f and the Gibbs energy of adsorption (DGads for each adsorbed phase were determined. In the case of iodide adsorption, four peaks were characterized by negative values of f, indicating attractive lateral interaction between the adsorbed anions, while two of them possessed value of f < –4, indicating phase transition processes. The adsorption/desorption processes of cadmium cations (underpotential deposition – UPD of cadmium in the presence of iodide anions was characterized by two main peaks, each of them being composed of two or three peaks with negative values of f. By the analysis of charge vs. potential dependences obtained either from the CVs or current transients on potentiostatic pulses, it was concluded that adsorbed iodides did not undergo desorption during the process of Cd UPD, but became replaced by Cd ad-atoms and remained adsorbed on top of a Cd layer and/or in between Cd the ad-atoms.

Surface characterization of Ag/Titania adsorbents

International Nuclear Information System (INIS)

Samokhvalov, Alexander; Nair, Sachin; Duin, Evert C.; Tatarchuk, Bruce J.

2010-01-01

The Ag/Titania adsorbent for selective removal of the desulfurization-refractive polycyclic aromatic sulfur heterocycles (PASHs) from liquid hydrocarbon fuels was prepared, its total and the Ag specific surface area were determined and the surface reaction sites in the sorbent that may be active in the adsorptive selective desulfurization were characterized by several spectroscopic and surface science techniques. The sorbent contains Ag, Ti, O and spurious C on its surface, as by the XPS measurements. Silver is present as an oxide, as judged by the XPS Auger parameter (AP). The complementary electron spin resonance (ESR) spectroscopy confirms that the majority of Ag is present in the diamagnetic Ag 1+ form, with the minor concentration (∼0.1% of total Ag) present as Ag 2+ . The findings by XPS and ESR are confirmed by the XRD, UV-vis spectroscopy and thermodynamic considerations. The supported Ag is highly dispersed on the surface of the titania support, with the particle size of ∼30-60 A depending on Ag content, with an Ag specific surface area of ∼7-14 m 2 /g, vs. the total surface area of ∼114-58 m 2 /g.

Plasmid DNA linearization in the antibacterial action of a new fluorescent Ag nanoparticle-paracetamol dimer composite

Science.gov (United States)

Sahoo, Amaresh Kumar; Sk, Md Palashuddin; Ghosh, Siddhartha Sankar; Chattopadhyay, Arun

2011-10-01

Herein, we report the generation of a composite comprised of p-hydroxyacetanilide dimer and Ag nanoparticles (NPs) by reaction of AgNO3 and p-hydroxyacetanilide. The formation of the composite was established by UV-vis, FTIR and NMR spectroscopy, transmission electron microscopy and X-ray diffraction along with substantiation by mass spectrometry. Interestingly, the composite exhibited an emission spectrum with a peak at 435 nm when excited by light of wavelength 320 nm. The composite showed superior antimicrobial activity with respect to its individual components against a wide range of Gram positive and Gram negative bacteria at relatively low concentrations of Ag NPs and at which there was no apparent cytotoxicity against mammalian cells. Our results suggest that the composite strongly interacted with the bacterial cell walls leading to cell bursting. Interestingly, enhancement in the reactive oxygen species (ROS) generation in bacteria was observed in the presence of the composite. It is proposed that the ROS generation led to oxidation of the dimer to N-acetyl-p-benzoquinone imine (NAPQI). The generated NAPQI acted as a DNA gyrase inhibitor causing cell death following linearization of DNA.Herein, we report the generation of a composite comprised of p-hydroxyacetanilide dimer and Ag nanoparticles (NPs) by reaction of AgNO3 and p-hydroxyacetanilide. The formation of the composite was established by UV-vis, FTIR and NMR spectroscopy, transmission electron microscopy and X-ray diffraction along with substantiation by mass spectrometry. Interestingly, the composite exhibited an emission spectrum with a peak at 435 nm when excited by light of wavelength 320 nm. The composite showed superior antimicrobial activity with respect to its individual components against a wide range of Gram positive and Gram negative bacteria at relatively low concentrations of Ag NPs and at which there was no apparent cytotoxicity against mammalian cells. Our results suggest that the

A biodynamic understanding of dietborne and waterborne Ag uptake from Ag NPs in the sediment-dwelling oligochaete, Tubifex tubifex

Science.gov (United States)

Tangaa, Stine Rosendal; Winther-Nielsen, Margrethe; Selck, Henriette; Croteau, Marie-Noele

2018-01-01

Metal nanoparticles (Me-NPs) are increasingly used in various products, such as inks and cosmetics, enhancing the likelihood of their release into aquatic environments. An understanding of the mechanisms controlling their bioaccumulation and ecotoxicity in aquatic biota will help support environmental risk assessment. Here we characterized unidirectional parameters for uptake and elimination of silver (Ag) in the sediment-dwelling oligochaete Tubifex tubifex after waterborne (0.01–47 nmol Ag/L) and dietborne (0.4–482 nmol Ag/g dw sed.) exposures to Ag NPs and AgNO3, respectively. Worms accumulated Ag from AgNO3more efficiently than from Ag NPs during waterborne exposure. The Ag uptake rate constants from water were 8.2 L/g/d for AgNO3 and 0.34 L/g/d for Ag NPs. Silver accumulated from both forms was efficiently retained in tissues, as no significant loss of Ag was detected after up to 20 days of depuration in clean media. High mortality (~50%) during depuration (i.e. after 17 days) was only observed for worms exposed to waterborne AgNO3 (3 nmol/L). Sediment exposures to both Ag forms resulted in low accumulation, i.e., the uptake rate constants were 0.002 and 0.005 g/g/d for AgNO3 and Ag NPs, respectively. Avoidance was only observed for worms exposed to sediment amended with AgNO3. Incorporation of the estimated rate constants into a biodynamic model predicted that sediment is likely the most important route of uptake for Ag in both forms in ecologically relevant aquatic environments. However, inference of bioavailability from our estimations of Ag assimilation efficiencies (AE) suggests that Ag (AE: 3–12% for AgNO3 and 0.1–0.8% for Ag NPs) is weakly bioavailable from sediment for this species. Thus, Ag amended to sediment as NPs might not pose greater problems than 'conventional' Ag for benthic organisms such as T. tubifex.

Effect of nano/micro-Ag compound particles on the bio-corrosion, antibacterial properties and cell biocompatibility of Ti-Ag alloys.

Science.gov (United States)

Chen, Mian; Yang, Lei; Zhang, Lan; Han, Yong; Lu, Zheng; Qin, Gaowu; Zhang, Erlin

2017-06-01

In this research, Ti-Ag alloys were prepared by powder metallurgy, casting and heat treatment method in order to investigate the effect of Ag compound particles on the bio-corrosion, the antibacterial property and the cell biocompatibility. Ti-Ag alloys with different sizes of Ag or Ag-compounds particles were successfully prepared: small amount of submicro-scale (100nm) Ti 2 Ag precipitates with solid solution state of Ag, large amount of nano-scale (20-30nm) Ti 2 Ag precipitates with small amount of solid solution state of Ag and micro-scale lamellar Ti 2 Ag phases, and complete solid solution state of Ag. The mechanical tests indicated that both nano/micro-scale Ti 2 Ag phases had a strong dispersion strengthening ability and Ag had a high solid solution strengthening ability. Electrochemical results shown the Ag content and the size of Ag particles had a limited influence on the bio-corrosion resistance although nano-scale Ti 2 Ag precipitates slightly improved corrosion resistance. It was demonstrated that the nano Ag compounds precipitates have a significant influence on the antibacterial properties of Ti-Ag alloys but no effect on the cell biocompatibility. It was thought that both Ag ions release and Ti 2 Ag precipitates contributed to the antibacterial ability, in which nano-scale and homogeneously distributed Ti 2 Ag phases would play a key role in antibacterial process. Copyright © 2017 Elsevier B.V. All rights reserved.

Differential Phytotoxic Impact of Plant Mediated Silver Nanoparticles (AgNPs) and Silver Nitrate (AgNO3) on Brassica sp.

Science.gov (United States)

Vishwakarma, Kanchan; Shweta; Upadhyay, Neha; Singh, Jaspreet; Liu, Shiliang; Singh, Vijay P; Prasad, Sheo M; Chauhan, Devendra K; Tripathi, Durgesh K; Sharma, Shivesh

2017-01-01

Continuous formation and utilization of nanoparticles (NPs) have resulted into significant discharge of nanosized particles into the environment. NPs find applications in numerous products and agriculture sector, and gaining importance in recent years. In the present study, silver nanoparticles (AgNPs) were biosynthesized from silver nitrate (AgNO 3 ) by green synthesis approach using Aloe vera extract. Mustard ( Brassica sp.) seedlings were grown hydroponically and toxicity of both AgNP and AgNO 3 (as ionic Ag + ) was assessed at various concentrations (1 and 3 mM) by analyzing shoot and root length, fresh mass, protein content, photosynthetic pigments and performance, cell viability, oxidative damage, DNA degradation and enzyme activities. The results revealed that both AgNPs and AgNO 3 declined growth of Brassica seedlings due to enhanced accumulation of AgNPs and AgNO 3 that subsequently caused severe inhibition in photosynthesis. Further, the results showed that both AgNPs and AgNO 3 induced oxidative stress as indicated by histochemical staining of superoxide radical and hydrogen peroxide that was manifested in terms of DNA degradation and cell death. Activities of antioxidants, i.e., ascorbate peroxidase (APX) and catalase (CAT) were inhibited by AgNPs and AgNO 3. Interestingly, damaging impact of AgNPs was lesser than AgNO 3 on Brassica seedlings which was due to lesser accumulation of AgNPs and better activities of APX and CAT, which resulted in lesser oxidative stress, DNA degradation and cell death. The results of the present study showed differential impact of AgNPs and AgNO 3 on Brassica seedlings, their mode of action, and reasons for their differential impact. The results of the present study could be implied in toxicological research for designing strategies to reduce adverse impact of AgNPs and AgNO 3 on crop plants.

Differential Phytotoxic Impact of Plant Mediated Silver Nanoparticles (AgNPs and Silver Nitrate (AgNO3 on Brassica sp.

Directory of Open Access Journals (Sweden)

Kanchan Vishwakarma

2017-10-01

Full Text Available Continuous formation and utilization of nanoparticles (NPs have resulted into significant discharge of nanosized particles into the environment. NPs find applications in numerous products and agriculture sector, and gaining importance in recent years. In the present study, silver nanoparticles (AgNPs were biosynthesized from silver nitrate (AgNO3 by green synthesis approach using Aloe vera extract. Mustard (Brassica sp. seedlings were grown hydroponically and toxicity of both AgNP and AgNO3 (as ionic Ag+ was assessed at various concentrations (1 and 3 mM by analyzing shoot and root length, fresh mass, protein content, photosynthetic pigments and performance, cell viability, oxidative damage, DNA degradation and enzyme activities. The results revealed that both AgNPs and AgNO3 declined growth of Brassica seedlings due to enhanced accumulation of AgNPs and AgNO3 that subsequently caused severe inhibition in photosynthesis. Further, the results showed that both AgNPs and AgNO3 induced oxidative stress as indicated by histochemical staining of superoxide radical and hydrogen peroxide that was manifested in terms of DNA degradation and cell death. Activities of antioxidants, i.e., ascorbate peroxidase (APX and catalase (CAT were inhibited by AgNPs and AgNO3. Interestingly, damaging impact of AgNPs was lesser than AgNO3 on Brassica seedlings which was due to lesser accumulation of AgNPs and better activities of APX and CAT, which resulted in lesser oxidative stress, DNA degradation and cell death. The results of the present study showed differential impact of AgNPs and AgNO3 on Brassica seedlings, their mode of action, and reasons for their differential impact. The results of the present study could be implied in toxicological research for designing strategies to reduce adverse impact of AgNPs and AgNO3 on crop plants.

The production of 103Pd and 109Cd from a proton irradiated tandem natAg/natAg targets

International Nuclear Information System (INIS)

Ineza, C.; Mphahlele, J.

2014-01-01

This paper describes a new method for the production of 103 Pd and 109 Cd using the 66 MeV proton beam of iThemba LABS on a tandem natural silver target (Ag/Ag). The radiochemical separation of the Pd radionuclides ( 103 Pd, 100 Pd) from the bulk nat Ag was done using a Chelex-100 chelating resin column. The recovery of 103 Pd from the irradiated nat Ag target was found to be >98 % without any Ag or Rh impurities detected. The radiochemical separation of 109 Cd from the bulk nat Ag target was done by the precipitation of Ag ions by Cu followed by the separation of 109 Cd, traces of Ag, Cu 2+ and Rh using a AG1-X10 anion exchange resin column. The recovery yield of 109 Cd was >99 % without any Ag or Rh impurities detected. (author)

Inbuilt potential of YEM medium and its constituents to generate Ag/Ag₂O nanoparticles.

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G Yamal

Full Text Available We discovered that Yeast Extract Mannitol (YEM medium possessed immense potential to generate silver nanoparticles from AgNO3 upon autoclaving, which was evident from (i alteration in color of the medium; (ii peak at ∼410 nm in UV-Vis spectrum due to surface plasmon resonance specific to silver nanoparticles; and (iii TEM investigations. TEM coupled with EDX confirmed that distinct nanoparticles were composed of silver. Yeast extract and mannitol were key components of YEM medium responsible for the formation of nanoparticles. PXRD analysis indicated crystalline geometry and Ag/Ag2O phases in nanoparticles generated with YEM medium, yeast extract and mannitol. Our investigations also revealed that both mannitol and yeast extract possessed potential to convert ∼80% of silver ions in 0.5 mM AgNO3 to nanoparticles, on autoclaving for 30 min at 121°C under a pressure of 1.06 kg/cm(2. Addition of filter sterilized AgNO3 under ambient conditions to pre-autoclaved YEM medium and yeast extract brought about color change due to the formation of silver nanoparticles, but required prolonged duration. In general, even after 72 h intensity of color was significantly less than that recorded following autoclaving. Silver nanoparticles formed at room temperature were more heterogeneous compared to that obtained upon autoclaving. In summary, our findings demonstrated that (i YEM medium and its constituents promote synthesis of silver nanoparticles; and (ii autoclaving enhances rapid synthesis of silver nanoparticles by YEM medium, yeast extract and mannitol.

Electronic and optical properties of AgAlO{sub 2}: A first-principles study

Energy Technology Data Exchange (ETDEWEB)

Bhamu, K.C., E-mail: kcbhamu85@gmail.com; Priolkar, K.R.

2017-04-01

In this paper, we present electronic and optical properties of silver-based delafossite compound AgAlO{sub 2} (AAO). For the electronic properties, we have computed band structure and density of states. The origin of band structure is elucidated in terms of density of states. A significant contribution in band structure comes from Ag-4d and O-2p states around the Fermi level. The estimated band gap shows the indirect semiconducting nature of AAO having the band gap value of 2.34 eV. For the optical properties, we have calculated frequency dependent dielectric functions. The peaks in the imaginary component of dielectric function are explained by electronic transitions in the dispersion relation. Our computed results are in agreement with those available in the literature. The wide band gap and hence transparency for the UV and visible incident light photons makes AAO a precious material for transparent electronics. - Highlights: • Applied different-different types of exchange-correlations and potentials. • Becke–Johnson with Hubbard potential (BJ + U) is better for 2H-AgAlO{sub 2}. • Band gap is in reasonable agreement with experimentally reported. • Origin of energy bands is elucidated in terms of density of states. • 2H-AgAlO{sub 2} is a promising candidate for transparent electronics.

The influence of post-annealing treatment on the wettability of Ag+/Na+ ion-exchanged soda-lime glasses

International Nuclear Information System (INIS)

Razzaghi, Ahmad; Maleki, Maniya; Azizian-Kalandaragh, Yashar

2013-01-01

In this paper, the effect of thermal annealing and the duration of ion-exchange on the wetting parameters of the Ag + /Na + ion-exchanged glasses have been reported. The analysis of wetting angle in different post-annealing temperatures shows that the wetting angle is increased by increasing the annealing temperature. The wetting parameters of Ag + /Na + ion-exchanged glasses at different ion-exchanged periods of time have been also investigated. Scanning electron microscopy (SEM), UV–Visible spectroscopy and Fourier transform infrared (FTIR) spectroscopy have been used for determination of surface morphology and composition analysis of the prepared samples. The results of SEM show changes in the surface of the samples for different post-annealing temperatures. The optical characterization using UV–Vis spectroscopy shows an increase in the intensity of the absorption peak with increasing the ion-exchange duration. The FTIR spectroscopy confirms the formation of silver oxide material on the surface of Ag + /Na + ion-exchanged glasses.

Defining the Crime of Enforced Disappearance in Conformity with International Criminal Law: a New Frontier for Bangladesh

OpenAIRE

Md. Raisul Islam Sourav

2015-01-01

Enforced disappearance is regarded as a state-sponsored heinous international crime and has recently emerged as a wide-spread issue in Bangladesh. The political opposition is currently the main target of forced disappearances, though apolitical citizens have also been targeted. Most of the incidents are unsolved and law enforcement agencies have repeatedly denied their involvement. Internationally, the UN Convention for the Protection of All Persons from Enforced Disappearance was opened for ...

HBcrAg Identifies Patients Failing to Achieve HBeAg Seroconversion Treated with Pegylated Interferon Alfa-2b

Directory of Open Access Journals (Sweden)

Hui Ma

2016-01-01

Conclusions: Effective antiviral treatment can decrease HBcrAg levels in the serum. The NPVs of HBcrAg for predicting HBeAg seroconversion at 24-week follow-up was 100%, but the PPVs were not satisfactory (all <31%. The serum HBcrAg levels of the patients with HBeAg seroconversion at the end of the 24-week follow-up steadily declined or even became undetectable during the LTFU.

Ti-GO-Ag nanocomposite: the effect of content level on the antimicrobial activity and cytotoxicity

Directory of Open Access Journals (Sweden)

Jin J

2017-06-01

Full Text Available Jianfeng Jin,1,2 Li Zhang,3 Mengqi Shi,3 Yumei Zhang,3 Qintao Wang11State Key Laboratory of Military Stomatology and National Clinical Research Center for Oral Diseases and Shaanxi Engineering Research Center for Dental Materials and Advanced Manufacture, Department of Periodontology, School of Stomatology, The Fourth Military Medical University, Xi’an, 2Department of General Dentistry, Kunming Municipal Stomatology Hospital, Kunming, 3State Key Laboratory of Military Stomatology and National Clinical Research Center for Oral Diseases and Shaanxi Key Laboratory of Stomatology, Department of Prosthodontics, School of Stomatology, The Fourth Military Medical University, Xi’an, People’s Republic of China Abstract: Surface modification of titanium (Ti implants are extensively studied in order to obtain prominent biocompatibility and antimicrobial activity, especially preventing implant-associated infection. In this study, Ti substrates surface were modified by graphene oxide (GO thin film and silver (Ag nanoparticles via electroplating and ultraviolet reduction methods so as to achieve this purpose. Microstructures, distribution, quantities and spectral peaks of GO and Ag loading on the Ti sheets surface were characterized. GO-Ag-Ti multiphase nanocomposite exhibited excellent antimicrobial ability and anti-adherence performance. Subsequently, morphology, membrane integrity, apoptosis and relative genes expression of bacteria incubated on the Ti samples surface were monitored to reveal the bactericidal mechanism. Additionally, the cytotoxicity of Ti substrates incorporating GO thin film and Ag nanoparticles were investigated. GO-Ag-Ti composite configuration that have outstanding antibacterial properties will provide the foundation to study bone integration in vitro and in vivo in the future.Keywords: GO-Ag-Ti multiphase nanocomposite, microstructure and quantities, antibacterial activity, bactericidal mechanism, cytotoxicity

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.

Antibacterial biodegradable Mg-Ag alloys

Directory of Open Access Journals (Sweden)

D Tie

2013-06-01

Full Text Available The use of magnesium alloys as degradable metals for biomedical applications is a topic of ongoing research and the demand for multifunctional materials is increasing. Hence, binary Mg-Ag alloys were designed as implant materials to combine the favourable properties of magnesium with the well-known antibacterial property of silver. In this study, three Mg-Ag alloys, Mg2Ag, Mg4Ag and Mg6Ag that contain 1.87 %, 3.82 % and 6.00 % silver by weight, respectively, were cast and processed with solution (T4 and aging (T6 heat treatment.The metallurgical analysis and phase identification showed that all alloys contained Mg4Ag as the dominant β phase. After heat treatment, the mechanical properties of all Mg-Ag alloys were significantly improved and the corrosion rate was also significantly reduced, due to presence of silver. Mg(OH2 and MgO present the main magnesium corrosion products, while AgCl was found as the corresponding primary silver corrosion product. Immersion tests, under cell culture conditions, demonstrated that the silver content did not significantly shift the pH and magnesium ion release. In vitro tests, with both primary osteoblasts and cell lines (MG63, RAW 264.7, revealed that Mg-Ag alloys show negligible cytotoxicity and sound cytocompatibility. Antibacterial assays, performed in a dynamic bioreactor system, proved that the alloys reduce the viability of two common pathogenic bacteria, Staphylococcus aureus (DSMZ 20231 and Staphylococcus epidermidis (DSMZ 3269, and the results showed that the killing rate of the alloys against tested bacteria exceeded 90%. In summary, biodegradable Mg-Ag alloys are cytocompatible materials with adjustable mechanical and corrosion properties and show promising antibacterial activity, which indicates their potential as antibacterial biodegradable implant materials.

Ag diffusion in cubic silicon carbide

International Nuclear Information System (INIS)

Shrader, David; Khalil, Sarah M.; Gerczak, Tyler; Allen, Todd R.; Heim, Andrew J.; Szlufarska, Izabela; Morgan, Dane

2011-01-01

The diffusion of Ag impurities in bulk 3C-SiC is studied using ab initio methods based on density functional theory. This work is motivated by the desire to reduce transport of radioactive Ag isotopes through the SiC boundary layer in the Tristructural-Isotropic (TRISO) fuel pellet, which is a significant concern for the Very High Temperature Reactor (VHTR) nuclear reactor concept. The structure and stability of charged Ag and Ag-vacancy clusters in SiC are calculated. Relevant intrinsic SiC defect energies are also determined. The most stable state for the Ag impurity in SiC is found to be a Ag atom substituting on the Si sub-lattice and bound to a C vacancy. Bulk diffusion coefficients are estimated for different impurity states and values are all found to have very high activation energy. The impurity state with the lowest activation energy for diffusion is found to be the Ag interstitial, with an activation energy of approximately 7.9 eV. The high activation energies for Ag diffusion in bulk 3C-SiC cause Ag transport to be very slow in the bulk and suggests that observed Ag transport in this material is due to an alternative mechanism (e.g., grain boundary diffusion).

Effect of Heat Treatments on Microstructures and Tensile Properties of Cu-3 wt%Ag-0.5 wt%Zr Alloy

Science.gov (United States)

Chen, Gang; Wang, ChuanJie; Zhang, Ying; Yi, Cen; Zhang, Peng

2018-03-01

The microstructures and tensile properties of Cu-3 wt%Ag-0.5 wt%Zr alloy sheets under different aging treatments are investigated in this research. As one kind of precipitate, Ag nanoparticles with coherent orientation relationship with matrix precipitate. However, after the peak-age point, most of Ag nanoparticles grow into short rod shape with the interface translating to semi-coherent, which leads to the lower strength of over-aging sample. The yield strength is estimated by considering solid solute, grain boundary and precipitation strengthening mechanisms. The result shows that the Ag precipitates provide the main strengthening role. Then a constitutive equation representing the evolution of dislocation density with plastic strain is built by considering work-hardening behavior coming from shearable and non-shearable precipitates which is mainly the particles containing Zr. The flow stress contributed by shearable particle hardening is higher than that of non-shearable one. Due to the coarsening of grain boundary precipitates and low rate of damage accumulation of these non-shearable particles, the micro-cracks nucleate easily at grain boundary which leads to intergranular fracture.

Defining the Crime of Enforced Disappearance in Conformity with International Criminal Law: a New Frontier for Bangladesh

Directory of Open Access Journals (Sweden)

Md. Raisul Islam Sourav

2015-12-01

Full Text Available Enforced disappearance is regarded as a state-sponsored heinous international crime and has recently emerged as a wide-spread issue in Bangladesh. The political opposition is currently the main target of forced disappearances, though apolitical citizens have also been targeted. Most of the incidents are unsolved and law enforcement agencies have repeatedly denied their involvement. Internationally, the UN Convention for the Protection of All Persons from Enforced Disappearance was opened for signature in 2007 and entered into force in 2010. The convention’s purpose is to criminalise enforced disappearances across the world and state parties are under an obligation to take necessary actions to stop their occurrence. Despite the cruel reality of forced disappearances in Bangladesh, no law has of yet been adopted to bring national criminal law in line with the convention. The right to life is nevertheless one of the key fundamental rights guaranteed under the Bangladeshi constitution which may be relevant in this context.  Forced disappearances have a disastrous impact on victim’s family as well as important societal implications. Bangladesh should, in this author’s opinion, ratify the convention and must reform national legislation to bring to an end state-sponsored crime. The scope of the issue may otherwise have tremendous consequences for the whole nation.

Comparison of partial structures of melts of superionic AgI and CuI and non-superionic AgCl

Energy Technology Data Exchange (ETDEWEB)

Kawakita, Yukinobu [Department of Physics, Faculty of Sciences, Kyushu University, 4-2-1 Ropponmatsu, Fukuoka 810-8560 (Japan); Tahara, Shuta [Department of Condensed Matter Chemistry and Physics, Graduate School of Sciences, Kyushu University, 4-2-1 Ropponmatsu, Chuo-ku, Fukuoka 810-8560 (Japan); Fujii, Hiroyuki [Department of Condensed Matter Chemistry and Physics, Graduate School of Sciences, Kyushu University, 4-2-1 Ropponmatsu, Chuo-ku, Fukuoka 810-8560 (Japan); Kohara, Shinji [Research and Utilization Division, Japan Synchrotron Radiation Research Institute (JASRI, SPring-8), 1-1-1 Koto, Sayo-cho, Sayo-gun, Hyogo 679-5198 (Japan); Takeda, Shin' ichi [Department of Physics, Faculty of Sciences, Kyushu University, 4-2-1 Ropponmatsu, Fukuoka 810-8560 (Japan)

2007-08-22

Neutron and high-energy x-ray diffraction analyses of molten AgI have been performed and the partial structures are discussed in detail with the aid of the structural modelling procedure of the reverse Monte Carlo (RMC) technique by comparison with those of molten CuI and AgCl. It is well known that AgI and CuI have a superionic solid phase below the melting point, in which the cations favour a tetrahedral configuration, while solid AgCl has a rock-salt structure with an octahedral environment around both Ag and Cl atoms. Even in the molten states, there is a significant difference between superionic and non-superionic melts. The cation is located on the triangular plain formed by three iodine ions in molten AgCl and CuI, while molten AgCl favours a 90 deg. Cl-Ag-Cl bond angle, which is understood to maintain a similar local environment to that in the solid state. The atomic configurations of the RMC model suggest that the cation distributions in superionic melts of CuI and AgI exhibit large fluctuations, while Ag ions in the non-superionic melts of AgCl are distributed much more uniformly.

Antigens of hepatitis B virus: failure to detect HBeAg on the surfaces of HBsAg forms

Energy Technology Data Exchange (ETDEWEB)

Gerin, J L [Oak Ridge National Lab., Rockville, MD; Shih, J W.K.; McAuliffee, V J; Purcell, R H

1978-01-01

The particulate forms of HBsAg were analysed for the presence of HBeAG on their surfaces. By immunodiffusion analysis, anti-HBe did not form precipitin bands with the purified forms of HBsAg and hyperimmune guinea pig antisera to these forms did not react with HBeAg. Lines of non-identity were observed between the HBeAg determinants (e/sub 1/ and e/sub 2/) and the Dane particles and filaments isolated from an HBeAg-positive serum. Finally, anti-HBe failed to precipitate the polymerase-positive subpopulation of Dane particles, indicating that anti-HBe has no direct role in virus neutralization.

The effect of soil properties on the toxicity and bioaccumulation of Ag nanoparticles and Ag ions in Enchytraeus crypticus.

Science.gov (United States)

Topuz, Emel; van Gestel, Cornelis A M

2017-10-01

Standard natural Lufa soils (2.2, 2.3 and 5M) with different organic carbon contents (0.67-1.61%) and pH CaCl2 (5.5-7.3) were spiked with ionic Ag (AgNO 3 ) and polyvinyl pyrrolidone (AgNP-PVP) and citrate (AgNP-Cit) coated Ag nanoparticles (NPs). Enchytraeus crypticus were exposed for 21 days to assess effects on survival and reproduction. Soil, pore water and animals were analyzed for Ag. AgNP-Cit had a strong increasing effect on soil pH, leading to high enchytraeid mortality at concentrations higher than 60-100mg Ag/kg dry soil which made it impossible to determine the influence of soil properties on its toxicity. LC50s were lower for AgNO 3 than for AgNP-PVP (92-112 and 335-425mg Ag/kg dry soil, respectively) and were not affected by soil properties. AgNO 3 and AgNP-PVP had comparable reproductive toxicity with EC50s of 26.9-75.2 and 28.2-92.3mg Ag/kg dry soil, respectively; toxicity linearly increased with decreasing organic carbon content of the soils but did not show a clear effect of soil pH. Ag uptake in the enchytraeids was higher at higher organic carbon content, but could not explain differences in toxicity between soils. This study indicates that the bioavailability of both ionic and nanoparticulate Ag is mainly affected by soil organic carbon, with little effect of soil pH. Copyright © 2017. Published by Elsevier Inc.

Control of texture in Ag and Ag-alloy substrates for superconducting tapes

International Nuclear Information System (INIS)

Gladstone, T.A.

2000-01-01

The use of a biaxially textured silver tape as a substrate for high temperature superconductor (HTS) phases is one possible route towards the fabrication of high-J c superconducting tape. Using a cold-rolling and annealing process we have reproducibly fabricated {110} textured silver which is stable up to 900 deg. C. We have found that there are two critical process requirements for the formation of this texture; a low oxygen content in the material prior to deformation, and a cold-rolling thickness reduction of less than 97%. To overcome the problems associated with the poor mechanical strength of pure silver, texture development in Ag-Mg and Ag-Hf alloys with improved mechanical properties has been studied. Heat treatments in a reducing atmosphere allow the {110} annealing texture to be obtained in Ag-0.1 wt%Mg. The recrystallization behaviour of a Ag-Pd alloy with an increased stacking fault energy was also investigated and a partial cube texture was obtained in this material. Using orientation distribution function (ODF) analysis we have shown that minor variations in the deformation texture of both pure silver and Ag-based alloys can lead to significant differences in the recrystallization textures obtained. (author)

Identification of Ag and Cd photoluminescence in $^{111}$Ag-doped GaN

CERN Document Server

Stötzler, A; Deicher, M

1999-01-01

In order to unambiguously identify the chemical nature of Cd and Ag related optical transitions in GaN, epitaxial GaN layers were implanted with the radioactive isotope $^{111}$Ag which decays into stable $^{111}$Cd. This chemical transmutation was monitored by photoluminescence (PL) spectroscopy. Being an element specific property, the half-life of this decay was used to establish the chemical assignment of the optical transitions to a specific defect. We found that the Ag related transitions consist of a series of four single lines (1.610, 1.600, 1.594, and 1.573 eV), each accompanied by two phonon replicas separated by 63 meV. Cd produces two PL bands centered at 2.7 and 3.2 eV. Additional Cd-related single transitions at 3.341, 3.328, and 3.249 eV have been observed. Exponential fits to the PL intensities yield half-lives of $t_{1/2}^{Ag}$= (7.61$\\pm$0.27) d and $t_{1/2}^{Cd}$=(7.60$\\pm$0.27) d, respectively, in good agreement with the half-life of $^{111}$Ag of 7.45 d. (13 refs).

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

Ferromagnetic resonance study of Fe{sub 50}Ag{sub 50} granular film

Energy Technology Data Exchange (ETDEWEB)

Sarmiento, G. [Dpto. Electricicidad y Electronica, Universidad del Pais Vasco (UPV/EHU), Apdo. 644, 48080 Bilbao (Spain)]. E-mail: websamug@lg.ehu.es; Fdez-Gubieda, M.L. [Dpto. Electricicidad y Electronica, Universidad del Pais Vasco (UPV/EHU), Apdo. 644, 48080 Bilbao (Spain); Siruguri, V. [Dpto. Electricicidad y Electronica, Universidad del Pais Vasco (UPV/EHU), Apdo. 644, 48080 Bilbao (Spain); UGC-DAE Consortium for Scientific Research, R-5 Shed, BARC Campus, Mumbai 400085 (India); Lezama, L. [Dpto. Quimica Inorganica (UPV/EHU), Apdo. 644, 48080, Bilbao (Spain); Orue, I. [Servicios Generales de Investigacion (SGIKER), Vicerrectorado de Investigacion (UPV/EHU) (Spain)

2007-09-15

Fe{sub 50}Ag{sub 50} granular film, produced by the pulsed laser deposition technique, has been studied using ferromagnetic resonance (FMR) at temperatures ranging from 4 to 300K. Three different resonance modes are well observed in the whole temperature range. We have also studied the angular evolution of the resonance peaks at three different temperatures T=150, 250, 300K. The thermal and the angular evolution of the three resonance fields has been interpreted on the basis of the existence of different magnetic coupling between the Fe nanoparticles and a weakly magnetized interface.

Photoluminescence of additively iodine colored superionic conductor RbAg4I5

International Nuclear Information System (INIS)

Afanas'ev, M.M.; Goffman, V.G.; Kompan, M.E.

1987-01-01

Luminescence of additivily colored monocrystals of RbAg 4 I 5 ionic conductor has been investigated. Luminescence excitation was exercises by light of a 3.68 eV photon. The luminescence spectrum is show to undergo changes after additive coloring, namely, abrupt increase of intensity in the 423-435 nm range with appearance of a narrow maximum in the 425 nm range, relative increase of intensity of a short-wave peak at 377 nm. A collection of data obtained by luminescent methods permits to consider formation of the surface layer of silver iodide approved

Facile fabrication of Ag dendrite-integrated anodic aluminum oxide membrane as effective three-dimensional SERS substrate

Science.gov (United States)

Zhang, Cong-yun; Lu, Ya; Zhao, Bin; Hao, Yao-wu; Liu, Ya-qing

2016-07-01

A novel surface enhanced Raman scattering (SERS)-active substrate has been successfully developed, where Ag-dendrites are assembled on the surface and embedded in the channels of anodic aluminum oxide (AAO) membrane, via electrodeposition in AgNO3/PVP aqueous system. Reaction conditions were systematically investigated to attain the best Raman enhancement. The growth mechanism of Ag dendritic nanostructures has been proposed. The Ag dendrite-integrated AAO membrane with unique hierarchical structures exhibits high SERS activity for detecting rhodamine 6G with a detection limit as low as 1 × 10-11 M. Furthermore, the three-dimensional (3D) substrates display a good reproducibility with the average intensity variations at the major Raman peak less than 12%. Most importantly, the 3D SERS substrates without any surface modification show an outstanding SERS response for the molecules with weak affinity for noble metal surfaces. The potential application for the detection of polycyclic aromatic hydrocarbons (PAHs) was evaluated with fluoranthene as Raman target molecule and a sensitive SERS detection with a limit down to 10-8 M was reached. The 3D SERS-active substrate shows promising potential for rapid detection of trace organic pollutants even weak affinity molecules in the environment.

Quantitative optical extinction-based parametric method for sizing a single core-shell Ag-Ag2O nanoparticle

International Nuclear Information System (INIS)

Santillan, J M J; Scaffardi, L B; Schinca, D C

2011-01-01

This paper develops a parametric method for determining the core radius and shell thickness in small silver-silver-oxide core-shell nanoparticles (Nps) based on single particle optical extinction spectroscopy. The method is based on the study of the relationship between plasmon peak wavelength, full width at half maximum (FWHM) and contrast of the extinction spectra as a function of core radius and shell thickness. This study reveals that plasmon peak wavelength is strongly dependent on shell thickness, whereas FWHM and contrast depend on both variables. These characteristics may be used for establishing an easy and fast stepwise procedure to size core-shell NPs from single particle absorption spectrum. The importance of the method lies in the possibility of monitoring the growth of the silver-oxide layer around small spherical silver Nps in real time. Using the electrostatic approximation of Mie theory, core-shell single particle extinction spectra were calculated for a silver particle's core size smaller than about 20 nm and different thicknesses of silver oxide around it. Analysis of the obtained curves shows a very particular characteristic of the plasmon peak of small silver-silver-oxide Nps, expressed in the fact that its position is strongly dependent on oxide thickness and weakly dependent on the core radius. Even a very thin oxide layer shifts the plasmon peak noticeably, enabling plasmon tuning with appropriate shell thickness. This characteristic, together with the behaviour of FWHM and contrast of the extinction spectra can be combined into a parametric method for sizing both core and shell of single silver Nps in a medium using only optical information. In turn, shell thickness can be related to oxygen content in the Np's surrounding media. The method proposed is applied to size silver Nps from single particle extinction spectrum. The results are compared with full optical spectrum fitting using the electrostatic approximation in Mie theory. The method

Ag@Ag{sub 8}W{sub 4}O{sub 16} nanoroasted rice beads with photocatalytic, antibacterial and anticancer activity

Energy Technology Data Exchange (ETDEWEB)

Selvamani, Muthamizh; Krishnamoorthy, Giribabu; Ramadoss, Manigandan; Sivakumar, Praveen Kumar; Settu, Munusamy [Department of Inorganic Chemistry, University of Madras, Guindy Campus, Chennai, 600 025 (India); Ranganathan, Suresh [Department of Chemistry, SRM University, Ramapuram Campus, Chennai, 600 089 (India); Vengidusamy, Narayanan, E-mail: vnnara@yahoo.co.in [Department of Inorganic Chemistry, University of Madras, Guindy Campus, Chennai, 600 025 (India)

2016-03-01

Increasing resistance of pathogens and cancer cell line towards antibiotics and anticancer agents has caused serious health problems in the past decades. Due to these problems in recent years, researchers have tried to combine nanotechnology with material science to have intrinsic antimicrobial and anticancer activity. The metals and metal oxides were investigated with respect to their antimicrobial and anticancer effects towards bacteria and cancer cell line. In the present work metal@metal tungstate (Ag@Ag{sub 8}W{sub 4}O{sub 16} nanoroasted rice beads) is investigated for antibacterial activity against Escherichia coli and Staphylococcus aureus using Mueller-Hinton broth and the anticancer activity against B16F10 cell line was studied. Silver decorated silver tungstate (Ag@Ag{sub 8}W{sub 4}O{sub 16}) was synthesized by the microwave irradiation method using Cetyl Trimethyl Ammonium Bromide (CTAB). Ag@Ag{sub 8}W{sub 4}O{sub 16} was characterized by using various spectroscopic techniques. The phase and crystalline nature were analyzed by using XRD. The morphological analysis was carried out using Field Emission Scanning Electron Microscopy (FE-SEM), and High Resolution Transmission Electron Microscopy (HR-TEM). Further, Fourier Transform Infrared Spectroscopy (FT-IR) and Raman spectral analysis were carried out in order to ascertain the presence of functional groups in Ag@Ag{sub 8}W{sub 4}O{sub 16}. The optical property was investigated using Diffuse Reflectance Ultraviolet–Visible Spectroscopy (DRS-UV–Vis) and the band gap was found to be 3.08 eV. Surface area of the synthesized Ag@Ag{sub 8}W{sub 4}O{sub 16} wasanalyzed by BET analysis and Ag@Ag{sub 8}W{sub 4}O{sub 16} was utilized for the degradation of organic dyes methylene blue and rhodamine B. The morphology of the Ag@Ag{sub 8}W{sub 4}O{sub 16} resembles roasted rice beads with breath and length in nm range. The oxidation state of tungsten (W) and silver (Ag) was investigated using X-ray photoelectron

Analysis of hepatitis B surface antigen (HBsAg) using high-sensitivity HBsAg assays in hepatitis B virus carriers in whom HBsAg seroclearance was confirmed by conventional assays.

Science.gov (United States)

Ozeki, Itaru; Nakajima, Tomoaki; Suii, Hirokazu; Tatsumi, Ryoji; Yamaguchi, Masakatsu; Kimura, Mutsuumi; Arakawa, Tomohiro; Kuwata, Yasuaki; Ohmura, Takumi; Hige, Shuhei; Karino, Yoshiyasu; Toyota, Joji

2018-02-01

We investigated the utility of high-sensitivity hepatitis B surface antigen (HBsAg) assays compared with conventional HBsAg assays. Using serum samples from 114 hepatitis B virus (HBV) carriers in whom HBsAg seroclearance was confirmed by conventional HBsAg assays (cut-off value, 0.05 IU/mL), the amount of HBsAg was re-examined by high-sensitivity HBsAg assays (cut-off value, 0.005 IU/mL). Cases negative for HBsAg in both assays were defined as consistent cases, and cases positive for HBsAg in the high-sensitivity HBsAg assay only were defined as discrepant cases. There were 55 (48.2%) discrepant cases, and the range of HBsAg titers determined by high-sensitivity HBsAg assays was 0.005-0.056 IU/mL. Multivariate analysis showed that the presence of nucleos(t)ide analog therapy, liver cirrhosis, and negative anti-HBs contributed to the discrepancies between the two assays. Cumulative anti-HBs positivity rates among discrepant cases were 12.7%, 17.2%, 38.8%, and 43.9% at baseline, 1 year, 3 years, and 5 years, respectively, whereas the corresponding rates among consistent cases were 50.8%, 56.0%, 61.7%, and 68.0%, respectively. Hepatitis B virus DNA negativity rates were 56.4% and 81.4% at baseline, 51.3% and 83.3% at 1 year, and 36.8% and 95.7% at 3 years, among discrepant and consistent cases, respectively. Hepatitis B surface antigen reversion was observed only in discrepant cases. Re-examination by high-sensitivity HBsAg assays revealed that HBsAg was positive in approximately 50% of cases. Cumulative anti-HBs seroconversion rates and HBV-DNA seroclearance rates were lower in these cases, suggesting a population at risk for HBsAg reversion. © 2017 The Japan Society of Hepatology.

Ozone decomposition on Ag/SiO{sub 2} and Ag/clinoptilolite catalysts at ambient temperature

Energy Technology Data Exchange (ETDEWEB)

Nikolov, Penko, E-mail: penmail@mail.bg [Institute of Catalysis, Bulgarian Academy of Sciences, 1113 Sofia (Bulgaria); Genov, Krassimir; Konova, Petya [Institute of General and Inorganic Chemistry, Bulgarian Academy of Sciences, 1113 Sofia (Bulgaria); Milenova, Katya; Batakliev, Todor; Georgiev, Vladimir [Institute of Catalysis, Bulgarian Academy of Sciences, 1113 Sofia (Bulgaria); Kumar, Narendra [Laboratory of Industrial Chemistry, Process Chemistry Centre, Abo Akademi University, Biskopsgatan 8, 20500 Abo/Turku (Finland); Sarker, Dipak K. [School of Pharmacy and Biomolecular Sciences, University of Brighton, Lewes Road, Brighton BN2 4GJ (United Kingdom); Pishev, Dimitar [University of Chemical Technology and Metallurgy, 1756 Sofia (Bulgaria); Rakovsky, Slavcho [Institute of Catalysis, Bulgarian Academy of Sciences, 1113 Sofia (Bulgaria)

2010-12-15

Silver modified zeolite (Bulgarian natural clinoptilolite) and Ag/silica catalysts were synthesized by ion exchange and incipient wet impregnation method respectively and characterized by different techniques. DC arc-AES was used for Ag detection. XRD spectra show that Ag is loaded over the surface of the SiO{sub 2} sample and that after the ion-exchange process the HEU type structure of clinoptilolite is retained. UV-VIS (specific reflection at 310 nm) and IR (band at 695 cm{sup -1}) spectroscopy analysis proved that silver is loaded as a T-atom into zeolite channels as Ag{sup +}, instead of Na{sup +}, Ca{sup 2+}, or K{sup +} ions, existing in the natural clinoptilolite form. The samples Ag/SiO{sub 2} and Ag-clinoptilolite were tested as catalysts for decomposition of gas phase ozone. Very high catalytic activity (up to 99%) was observed and at the same time the catalysts remained active over time at room temperature.

Synthesis and characterizations of spherical hollow composed of AgI nanoparticle using AgBr as the precursor

International Nuclear Information System (INIS)

Yang Ming; Zhou Kui

2011-01-01

Hollow spheres of AgI with an average radius of 100-200 nm have been prepared by a simple reaction between AgBr suspension and KI in the presence of gelatin. Gelatin played a decisive role as an inhibitor of the direct attack of I - ions to AgBr surfaces and coagulation of the growing AgI in producing the spherical AgI particles. The products were characterized by X-ray powder diffraction, transmission electron microscopy, UV-vis absorption spectroscopy and X-ray photoelectron spectra techniques. The band gaps are estimated to be 2.95 eV according to the results of optical measurements of the hollow spheres of AgI.

Fabrication of Z-scheme plasmonic photocatalyst Ag@AgBr/g-C3N4 with enhanced visible-light photocatalytic activity

International Nuclear Information System (INIS)

Yang, Yuxin; Guo, Wan; Guo, Yingna; Zhao, Yahui; Yuan, Xing; Guo, Yihang

2014-01-01

Graphical abstract: - Highlights: • Z-scheme plasmonic photocatalyst of Ag@AgBr/g-C 3 N 4 is prepared for the first time. • Ag@AgBr/g-C 3 N 4 shows enhanced visible-light photocatalytic activity. • Photocatalytic mechanism based on the experimental results is revealed. • Photocatalytic degradation pathway of MO is put forward. - Abstract: A series of Ag@AgBr grafted graphitic carbon nitride (Ag@AgBr/g-C 3 N 4 ) plasmonic photocatalysts are fabricated through photoreducing AgBr/g-C 3 N 4 hybrids prepared by deposition–precipitation method. The phase and chemical structures, electronic and optical properties as well as morphologies of Ag@AgBr/g-C 3 N 4 heterostructures are well-characterized. Subsequently, the photocatalytic activity of Ag@AgBr/g-C 3 N 4 is evaluated by the degradation of methyl orange (MO) and rhodamin B (RB) under visible-light irradiation. The enhanced photocatalytic activity of Ag@AgBr/g-C 3 N 4 compared with g-C 3 N 4 and Ag@AgBr is obtained and explained in terms of the efficient visible-light utilization efficiency as well as the construction of Z-scheme, which keeps photogenerated electrons and holes with high reduction and oxidation capability, evidenced by photoelectrochemical tests and free radical and hole scavenging experiments. Based on the intermediates identified in the reaction system, the photocatalytic degradation pathway of MO is put forward

Nano Ag@AgBr surface-sensitized Bi{sub 2}WO{sub 6} photocatalyst: oil-in-water synthesis and enhanced photocatalytic degradation

Energy Technology Data Exchange (ETDEWEB)

Lin, Shuanglong; Liu, Li; Hu, Jinshan; Liang, Yinghua, E-mail: liangyh@heuu.edu.cn; Cui, Wenquan, E-mail: wkcui@163.com

2015-01-01

Graphical abstract: - Highlights: • The plasmatic Ag@AgBr surface-sensitized Bi{sub 2}WO{sub 6} composite photocatalysts. • Ag@AgBr greatly increased visible-light absorption for Bi{sub 2}WO{sub 6}. • The plasmonic photocatalysts exhibited enhanced activity for the degradation of MB, phenol and salicylic acid. - Abstract: Nano Ag@AgBr decorated on the surface of flower-like Bi{sub 2}WO{sub 6} (hereafter designated Ag@AgBr/Bi{sub 2}WO{sub 6}) were prepared via a facile oil-in-water self-assembly method. The photocatalysts were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV–vis diffuse reflectance spectroscopy (DRS), etc. The characterization results indicated that nano Ag@AgBr was observed to be evenly dispersed on the surface of Bi{sub 2}WO{sub 6}, and was approximately 20 nm in size. Ag@AgBr/Bi{sub 2}WO{sub 6} composites exhibited excellent UV–vis absorption, due to quantum dimension effect of Ag@AgBr, the surface plasmonic resonance (SPR) of Ag nanoparticles and the special flower-like structure of Bi{sub 2}WO{sub 6}. The photoelectrochemical measurement verified that the suitable band potential of Ag@AgBr and Bi{sub 2}WO{sub 6} and the existence of metal Ag resulted in the high efficiency in charge separation of the composite. The photocatalytic activities of the Ag@AgBr/Bi{sub 2}WO{sub 6} samples were examined under visible-light irradiation for the degradation of methylene blue (MB). The composite presented excellent photocatalytic activity due to the synergetic effect of Bi{sub 2}WO{sub 6}, AgBr, and Ag nanoparticles. The Ag@AgBr(20 wt.%)/Bi{sub 2}WO{sub 6} sample exhibited the best photocatalytic activity, degrading 95.03% MB after irradiation for 2 h, which was respectively 1.29 times and 1.28 times higher than that of Ag@AgBr and Bi{sub 2}WO{sub 6} photocatalyst. Meanwhile, phenol and salicylic acid were degraded to further prove the degradation ability of Ag@AgBr/Bi{sub 2

Posintro™-HBsAg, a modified ISCOM including HBsAg, induces strong cellular and humoral responses

DEFF Research Database (Denmark)

Schiött, Asa; Larsson, Kristina; Manniche, Søren

2011-01-01

HBsAg vaccine formulation, Posintro™-HBsAg, was compared to two commercial hepatitis B vaccines including aluminium or monophosphoryl lipid A (MPL) and the two adjuvant systems MF59 and QS21 in their efficiency to prime both cellular and humoral immune responses. The Posintro™-HBsAg induced...

Fabrication of AgX-loaded Ag2CO3 (X = Cl, I) composites and their efficient visible-light-driven photocatalytic activity

International Nuclear Information System (INIS)

Xu, Hui; Zhu, Jiaxiang; Song, Yongxiu; Zhu, Tingting; Zhao, Wenkai; Song, Yanhua; Da, Zulin; Liu, Chengbao; Li, Huaming

2015-01-01

Highlights: • The novel AgX/Ag 2 CO 3 composites have been synthesized by ion exchange reaction. • AgX/Ag 2 CO 3 exhibit higher photoactivity and stability than that of Ag 2 CO 3 . • The band structure of AgX/Ag 2 CO 3 is beneficial to improve the photoactivity. - Abstract: The novel visible-light-driven AgX/Ag 2 CO 3 (X = Cl, I) hybrid materials were synthesized by ion exchange reaction. The physical and chemical properties of the catalysts were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), energy dispersive spectrometer (EDS), transmission electron microscopy (TEM), diffuse-reflection spectra (DRS) and photocurrent techniques. The as-prepared AgX/Ag 2 CO 3 (X = Cl, I) composites showed higher photocatalytic activity than that of the pure Ag 2 CO 3 photocatalyst under visible light irradiation (λ ⩾ 400 nm) in the process of methylene blue (MB) degradation. The optimal mass percentage of AgCl and AgI in the AgX/Ag 2 CO 3 (X = Cl, I) composite was 20.54 wt% and 40 wt%, respectively. The enhancement of photocatalytic activity was attributed to the suitable band potential between AgX and Ag 2 CO 3 , which was beneficial to increase the separation efficiency of electrons and holes. Besides, the photocatalytic mechanism of AgX/Ag 2 CO 3 (X = Cl, I) composites was also proposed

Application of a newly developed high-sensitivity HBsAg chemiluminescent enzyme immunoassay for hepatitis B patients with HBsAg seroclearance.

Science.gov (United States)

Shinkai, Noboru; Matsuura, Kentaro; Sugauchi, Fuminaka; Watanabe, Tsunamasa; Murakami, Shuko; Iio, Etsuko; Ogawa, Shintaro; Nojiri, Shunsuke; Joh, Takashi; Tanaka, Yasuhito

2013-11-01

We modified and automated a highly sensitive chemiluminescent enzyme immunoassay (CLEIA) for surface antigen (HBsAg) detection using a combination of monoclonal antibodies, each for a specific epitope of HBsAg, and by improving an earlier conjugation technique. Of 471 hepatitis B virus (HBV) carriers seen in our hospital between 2009 and 2012, 26 were HBsAg seronegative as determined by the Abbott Architect assay. The Lumipulse HBsAg-HQ assay was used to recheck those 26 patients who demonstrated seroclearance by the Abbott Architect assay. The performance of the Lumipulse HBsAg-HQ assay was compared with that of a quantitative HBsAg detection system (Abbott Architect) and the Roche Cobas TaqMan HBV DNA assay (CTM) (lower limit of detection, 2.1 log copies/ml) using blood serum samples from patients who were determined to be HBsAg seronegative by the Abbott Architect assay. Ten patients had spontaneous HBsAg loss. Of 8 patients treated with nucleotide analogues (NAs), two were HBsAg seronegative after stopping lamivudine therapy and 6 were HBsAg seronegative during entecavir therapy. Eight acute hepatitis B (AH) patients became HBsAg seronegative. Of the 26 patients, 16 were HBsAg positive by the Lumipulse HBsAg-HQ assay but negative by the Abbott Architect assay. The differences between the two assays in terms of detectable HBsAg persisted over the long term in the spontaneous loss group (median, 10 months), the NA-treated group (2.5 months), and the AH group (0.5 months). In 9 patients, the Lumipulse HBsAg-HQ assay detected HBsAg when HBV DNA was negative by the CTM assay. HBsAg was also detected by the Lumipulse HBsAg-HQ assay in 4 patients with an anti-HBs concentration of >10 mIU/ml, 3 of whom had no HBsAg escape mutations. The automatic, highly sensitive HBsAg CLEIA Lumipulse HBsAg-HQ is a convenient and precise assay for HBV monitoring.

Disappearing neutrinos at KamLAND suport the case for neutrino mass

CERN Multimedia

Johnson, G

2002-01-01

Measurements from KamLAND, show that anti-neutrinos emanating from nearby nuclear reactors are "disappearing," which indicates they have mass and can oscillate or change from one type to another (2 pages)

Ag/ZnO hybrid systems studied with scanning tunnelling microscopy-based luminescence spectroscopy

International Nuclear Information System (INIS)

Pascua, Leandro; Freund, Hans-Joachim; Stavale, Fernando; Nilius, Niklas

2016-01-01

Coupled metal/oxide systems are prepared by depositing and embedding Ag nanoparticles into crystalline ZnO films grown on Au(111) supports. The morphology and optical properties of the compounds are investigated by topographic imaging and luminescence spectroscopy performed in a scanning tunnelling microscope (STM). The luminescence of bare ZnO is governed by the band-recombination and a Zn-vacancy related peak. After Ag deposition, two additional maxima are detected that are assigned to the in-plane and out-of-plane plasmon in Ag nanoparticles and have energies below and slightly above the oxide band-gap, respectively. Upon coating the particles with additional ZnO, the out-of-plane plasmon redshifts and loses intensity, indicating strong coupling to the oxide electronic system, while the in-plane mode broadens but remains detectable. The original situation can be restored by gently heating the sample, which drives the silver back to the surface. However, the optical response of pristine ZnO is not recovered even after silver evaporation at high temperature. Small discrepancies are explained with changes in the ZnO defect landscape, e.g., due to silver incorporation. Our experiments demonstrate how energy-transfer processes can be investigated in well-defined metal/oxide systems by means of STM-based spectroscopic techniques.

Ag/ZnO hybrid systems studied with scanning tunnelling microscopy-based luminescence spectroscopy

Energy Technology Data Exchange (ETDEWEB)

Pascua, Leandro; Freund, Hans-Joachim [Fritz-Haber-Institut der Max-Planck-Gesellschaft, Faradayweg 4-6, D-14195 Berlin (Germany); Stavale, Fernando [Fritz-Haber-Institut der Max-Planck-Gesellschaft, Faradayweg 4-6, D-14195 Berlin (Germany); Centro Brasileiro de Pesquisas Físicas - CBPF/MCTI, Rua Xavier Sigaud 150, 22290-180 Rio de Janeiro (Brazil); Nilius, Niklas, E-mail: niklas.nilius@uni-oldenburg.de [Fritz-Haber-Institut der Max-Planck-Gesellschaft, Faradayweg 4-6, D-14195 Berlin (Germany); Institut für Physik, Carl von Ossietzky Universität Oldenburg, D-26111 Oldenburg (Germany)

2016-03-07

Coupled metal/oxide systems are prepared by depositing and embedding Ag nanoparticles into crystalline ZnO films grown on Au(111) supports. The morphology and optical properties of the compounds are investigated by topographic imaging and luminescence spectroscopy performed in a scanning tunnelling microscope (STM). The luminescence of bare ZnO is governed by the band-recombination and a Zn-vacancy related peak. After Ag deposition, two additional maxima are detected that are assigned to the in-plane and out-of-plane plasmon in Ag nanoparticles and have energies below and slightly above the oxide band-gap, respectively. Upon coating the particles with additional ZnO, the out-of-plane plasmon redshifts and loses intensity, indicating strong coupling to the oxide electronic system, while the in-plane mode broadens but remains detectable. The original situation can be restored by gently heating the sample, which drives the silver back to the surface. However, the optical response of pristine ZnO is not recovered even after silver evaporation at high temperature. Small discrepancies are explained with changes in the ZnO defect landscape, e.g., due to silver incorporation. Our experiments demonstrate how energy-transfer processes can be investigated in well-defined metal/oxide systems by means of STM-based spectroscopic techniques.

Interplay between Appearance and Disappearance Channels for Precision Measurements of θ₂₃ and δ

Energy Technology Data Exchange (ETDEWEB)

Coloma, Pilar; Minakata, Hisakazu; Parke, Stephen J.

2014-11-01

We discuss how the CP violating phase δ and the mixing angle θ₂₃ can be measured precisely in an environment where there are strong correlations between them. This is achieved by paying special attention to the mutual roles and the interplay between the appearance and the disappearance channels in long-baseline neutrino oscillation experiments. We analyze and clarify the general structure of the θ₂₃ - θ₁₃ - δ degeneracy for both the appearance and disappearance channels in a more complete fashion than what has previously been discussed in the literature. A full understanding of this degeneracy is of vital importance if θ₂₃ is close to maximal mixing. The relative importance between the appearance and disappearance channels depends upon the particular setup and how close to maximal mixing Nature has chosen the value for θ₂₃. For facilities that operate with a narrow band beam or a wide band beam centered on the first oscillation extremum, the contribution of the disappearance channel depends critically on the systematic uncertainties assumed for this channel. Whereas for facilities that operate at energies above the first oscillation extremum or at the second oscillation extremum the appearance channels dominate. On the other hand, for δ we find that the disappearance channel usually improves the sensitivity, modestly for facilities around the first oscillation extremum and more significantly for facilities operating at an energy above the first oscillation extremum, especially near δ ~ ± π/2.

A comparative study about electronic structures at rubrene/Ag and Ag/rubrene interfaces

Directory of Open Access Journals (Sweden)

Sumona Sinha

2015-10-01

Full Text Available The contact between the electrode and the organic semiconductor is one of the most crucial factors in determining the organic device performance. The development and production technology of different organic devices require the understanding of different types of metal/organic semiconducting thin film interfaces. Comparisons about the electronic structures at Rubrene/Ag and Ag/Rubrene interfaces have been studied using photoemission spectroscopy. The Ag on rubrene interfaces is found to show more interesting and complex natures than its counterpart. The vacuum level (VL was shifted about 0.51 eV from push back effect for deposition of 5 Å rubrene onto Ag film whereas the electronic features of silver was only suppressed and no energy shift was resulted. While the deposition of 5 Å Ag onto rubrene film leads to the diffusion of the Ag atoms, as a cluster with quantum size effect, inside the film. Angle dependent XPS measurement indicates that diffused metal clusters were present at entire probed depth of the film. Moreover these clusters dope the uppermost surface of the rubrene film which consequences a shift of the electronic states of thick organic film towards higher binding energy. The VL was found to shift about 0.31 eV toward higher binding energy whereas the shift was around 0.21 eV for the electronic states of rubrene layer.

A comparative study about electronic structures at rubrene/Ag and Ag/rubrene interfaces

Energy Technology Data Exchange (ETDEWEB)

Sinha, Sumona, E-mail: sumona.net.09@gmail.com; Mukherjee, M. [Saha Institute of Nuclear Physics, 1/AF, Bidhan Nagar, Kolkata 700064 (India)

2015-10-15

The contact between the electrode and the organic semiconductor is one of the most crucial factors in determining the organic device performance. The development and production technology of different organic devices require the understanding of different types of metal/organic semiconducting thin film interfaces. Comparisons about the electronic structures at Rubrene/Ag and Ag/Rubrene interfaces have been studied using photoemission spectroscopy. The Ag on rubrene interfaces is found to show more interesting and complex natures than its counterpart. The vacuum level (VL) was shifted about 0.51 eV from push back effect for deposition of 5 Å rubrene onto Ag film whereas the electronic features of silver was only suppressed and no energy shift was resulted. While the deposition of 5 Å Ag onto rubrene film leads to the diffusion of the Ag atoms, as a cluster with quantum size effect, inside the film. Angle dependent XPS measurement indicates that diffused metal clusters were present at entire probed depth of the film. Moreover these clusters dope the uppermost surface of the rubrene film which consequences a shift of the electronic states of thick organic film towards higher binding energy. The VL was found to shift about 0.31 eV toward higher binding energy whereas the shift was around 0.21 eV for the electronic states of rubrene layer.

Structural, optical and electrical characterization of ITO, ITO/Ag and ITO/Ni transparent conductive electrodes

Energy Technology Data Exchange (ETDEWEB)

Ali, Ahmad Hadi, E-mail: ahadi@uthm.edu.my [Nano-Optoelectronics Research and Technology Laboratory, School of Physics, Universiti Sains Malaysia, Penang (Malaysia); Science Department, Faculty of Science, Technology and Human Development, Universiti Tun Hussein Onn Malaysia, Johor (Malaysia); Shuhaimi, Ahmad [Low Dimensional Materials Research Centre, Department of Physics, Faculty of Science, Universiti Malaya, Kuala Lumpur (Malaysia); Hassan, Zainuriah [Nano-Optoelectronics Research and Technology Laboratory, School of Physics, Universiti Sains Malaysia, Penang (Malaysia)

2014-01-01

We report on the transparent conductive oxides (TCO) characteristics based on the indium tin oxides (ITO) and ITO/metal thin layer as an electrode for optoelectronics device applications. ITO, ITO/Ag and ITO/Ni were deposited on Si and glass substrate by thermal evaporator and radio frequency (RF) magnetron sputtering at room temperature. Post deposition annealing was performed on the samples in air at moderate temperature of 500 °C and 600 °C. The structural, optical and electrical properties of the ITO and ITO/metal were characterized using X-ray diffraction (XRD), UV–Vis spectrophotometer, Hall effect measurement system and atomic force microscope (AFM). The XRD spectrum reveals significant polycrystalline peaks of ITO (2 2 2) and Ag (1 1 1) after post annealing process. The post annealing also improves the visible light transmittance and electrical resistivity of the samples. Figure of merit (FOM) of the ITO, ITO/Ag and ITO/Ni were determined as 5.5 × 10{sup −3} Ω{sup −1}, 8.4 × 10{sup −3} Ω{sup −1} and 3.0 × 10{sup −5} Ω{sup −1}, respectively. The results show that the post annealed ITO with Ag intermediate layer improved the efficiency of the transparent conductive electrodes (TCE) as compared to the ITO and ITO/Ni.

Ag Isotopic Evolution of the Mantle During Accretion: New Constraints from Pd and Ag Metal-Silicate Partitioning

Science.gov (United States)

Righter, K.; Schonbachler, M.

2018-01-01

Decay of (sup 107) Pd to (sup 107) Ag has a half-life of 6.5 times 10 (sup 6) mega-annums. Because these elements are siderophile but also volatile, they offer potential constraints on the timing of core formation as well as volatile addition. Initial modelling has shown that the Ag isotopic composition of the bulk silicate Earth (BSE) can be explained if accretion occurs with late volatile addition. These arguments were tested for sensitivity for pre-cursor Pd/Ag contents, and for a fixed Pd/Ag ratio of the BSE of 0.1. New Ag and Pd partitioning data has allowed a better understanding of the partitioning behavior of Pd and Ag during core formation. The effects of S, C and Si, and the effect of high temperature and pressure has been evaluated. We can now calculate D(Ag) and D(Pd) over the wide range of PT conditions and variable metallic liquid compositions that are known during accretion. We then use this new partitioning information to revisit the Ag isotopic composition of the BSE during accretion.

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.

Preparation, characterization and photocatalytic activity of visible-light-driven plasmonic Ag/AgBr/ZnFe2O4 nanocomposites

International Nuclear Information System (INIS)

Li, Xiaojuan; Tang, Duanlian; Tang, Fan; Zhu, Yunyan; He, Changfa; Liu, Minghua; Lin, Chunxiang; Liu, Yifan

2014-01-01

Highlights: • A plasmonic Ag/AgBr/ZnFe 2 O 4 photocatalyst has been successfully synthesized. • Ag/AgBr/ZnFe 2 O 4 nanocomposites exhibit high visible light photocatalytic activity. • Ag/AgBr/ZnFe 2 O 4 photocatalyst is stable and magnetically separable. - Abstract: A visible-light-driven plasmonic Ag/AgBr/ZnFe 2 O 4 nanocomposite has been successfully synthesized via a deposition–precipitation and photoreduction through a novel one-pot process. X-ray diffraction spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscopy and UV–vis diffuse reflectance spectroscopy were employed to investigate the crystal structure, chemical composition, morphology, and optical properties of the as-prepared nanocomposites. The photocatalytic activities of the nanocomposites were evaluated by photodegradation of Rhodamine B (RhB) and phenol under visible light. The results demonstrated that the obtained Ag/AgBr/ZnFe 2 O 4 nanocomposites exhibited higher photocatalytic activity as compared to pure ZnFe 2 O 4 . In addition, the sample photoreduced for 20 min and calcined at 500 °C achieved the highest photocatalytic activity. Furthermore, the Ag/AgBr/ZnFe 2 O 4 nanocomposite has high stability under visible light irradiation and could be conveniently separated by using an external magnetic field

Ag nanoprisms with Ag₂S attachment.

KAUST Repository

Xiong, Shenglin; Xi, Baojuan; Zhang, Kang; Chen, Yifei; Jiang, Jianwen; Hu, Jiangyong; Zeng, Hua Chun

2013-01-01

Triangular Ag nanoprisms are a type of most-studied noble-metal nanostructures over the past decade owing to their special structural architecture and outstanding optical and catalytic properties for a wide range of applications. Nevertheless, in contrast to active research for the synthesis of phase-pure Ag nanoprisms, no asymmetric heterodimers containing Ag prisms have been developed so far, probably due to lack of suitable synthetic methods. Herein, we devise a simple ion-exchange method to synthesize Ag2S/Ag heterodimers at room temperature, through which Ag nanoprisms with controllable size and thickness can be fabricated. Formation chemistry and optical properties of the heterodimers have been investigated. These semiconductor/metal heterodimers have exhibited remarkable bactericidal activity to E. coli cells under visible light illumination.

Structural and optical characterization and efficacy of hydrothermal synthesized Cu and Ag doped zinc oxide nanoplate bactericides

Energy Technology Data Exchange (ETDEWEB)

Abinaya, C.; Marikkannan, M.; Manikandan, M. [Department of Materials Science, School of Chemistry, Madurai Kamaraj University, Madurai, 625 021, Tamil Nadu (India); Mayandi, J., E-mail: jeyanthinath@yahoo.co.in [Department of Materials Science, School of Chemistry, Madurai Kamaraj University, Madurai, 625 021, Tamil Nadu (India); Department of Materials Science and Engineering, Michigan Technological University, Houghton, 49931 1295, MI (United States); Suresh, P.; Shanmugaiah, V. [Department of Microbial Technology, School of Biological Sciences, Madurai Kamaraj University, Madurai, 625 021, Tamil Nadu (India); Ekstrum, C. [Department of Materials Science and Engineering, Michigan Technological University, Houghton, 49931 1295, MI (United States); Pearce, J.M. [Department of Materials Science and Engineering, Michigan Technological University, Houghton, 49931 1295, MI (United States); Department of Electrical & Computer Engineering, Michigan Technological University, Houghton, 49931 1295, MI (United States)

2016-12-01

This study reports on a novel synthesis of pure zinc oxide and both Cu and Ag doped ZnO nanoplates using a simple and low-cost hydrothermal method. The structural and optical properties of the nanoplates were quantified and the materials were tested for antibacterial activity. X-ray diffraction revealed the formation of the wurtzite phase of ZnO and scanning and transmission electron microscopy showed the formation of randomly oriented ZnO nanoplates, having a thickness less than 80 nm and diameter less than 350 nm. The elemental analyses of both the pure and doped samples were evaluated by energy dispersive X-ray spectrometry. The FTIR spectra of ZnO nanomaterials showed the predictable bands at 3385 cm{sup −1} (O−H stretching), 1637 cm{sup −1} (stretching vibration of H{sub 2}O), 400 cm{sup −1}–570 cm{sup −1} (M−O stretching). The as synthesized samples showed a strong absorption peak in the UV region (∼376 nm) and a near band edge emission at 392 nm with some defect peaks in the visible region. From the XPS spectra the oxidation states of Zn, Cu and Ag were found to be +2, +2 and 0 respectively. Escherichia coli, Staphylococcus aureus and Salmonella typhi bacteria were used to evaluate the antibacterial activity of undoped and doped ZnO. Ag doped ZnO exhibited low minimum inhibitory concentration (MIC) values as 40 μg/ml for E. coli and S. aureus and 20 μg/ml for S. typhi, which are comparable to commercial antibiotics without optimization. Further, these chemically modified nanoparticles will be applicable in the development of medicine to control the spread and infection of a variety of bacterial strains. - Highlights: • Distinct ZnO nanoplates were successfully synthesized by facile hydrothermal method. • Cu and Ag doped ZnO exhibits significant destruction of bacteria with low MIC value. • Ag:ZnO has a noteworthy bactericidal effect against E. coli, S. aureus &S. typhi. • It projects that, a feasible low cost industrial process can

Ultra-fine structures of Pd-Ag-HAp nanoparticle deposition on protruded TiO2 barrier layer for dental implant

Science.gov (United States)

Jang, Jae-Myung; Kim, Seung-Dai; Park, Tae-Eon; Choe, Han-Cheol

2018-02-01

The biocompatibility structure of an implant surface is of great importance to the formation of new bone tissue around the dental implant and also has a significant chemical reaction in the osseointegration process. Thus, ultra-fine Pd-Ag-HAp nanoparticles have been electrodeposited on protruded TiO2 barrier layer in mixed electrolyte solutions. Unusual protrusions patterns, which are assigned to Pd-Ag-HAp nanoparticles, can be clearly differentiated from a TiO2 nanotube oxide layer formed by an anodizing process. In the chemical bonding state, the surface characteristics of Pd/Ag/HAp compounds have been investigated by FE-SEM, EDS mapping analysis, and XPS analysis. The mapping dots of the elements including Ti, Ca, Pd, Ag, and P showed a homogeneous distribution throughout the entire surface when deposited onto the protruded TiO2 barrier layer. The XPS spectra of Ti-2p, O-1S, Pd-3d, and Ag-3d have been investigated, with the major XPS peak indicating Pd-3d. The Ag-3d level was clearly observed with further scanning of the Ca-2p region. Based on the results of the chemical states, the structural properties of the protrusion patterns were also examined after being deposited onto the barrier oxide film, resulting in the representative protrusion patterns being mainly composed of Pd-Ag-HAp compounds. The results of the soaking evaluation showed that the protrusion patterns and the protruded TiO2 barrier layer were all effective in regards to biocompatibility.

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)

Effects of annealing on the microstructure and magnetic property of the mechanically alloyed FeSiBAlNiM (M=Co, Cu, Ag) amorphous high entropy alloys

Energy Technology Data Exchange (ETDEWEB)

Zhu, Xiaoxia; Zhou, Xuan; Yu, Shuaishuai; Wei, Congcong; Xu, Jing; Wang, Yan, E-mail: mse_wangy@ujn.edu.cn

2017-05-15

The effects of annealing treatment on the microstructure, thermal stability, and magnetic properties of the mechanical alloyed FeSiBAlNiM (M=Co, Cu, Ag) amorphous high entropy alloys (HEAs) have been investigated in this project. The simple crystallization products in FeSiBAlNi amorphous HEAs with Co and Ag addition reveal the high phase stability during heating process. At high annealing treatment, the crystallized HEAs possess the good semi-hard magnetic property. It can conclude that crystallization products containing proper FeSi-rich and FeB-rich phases are beneficial to improve the magnetic property. Annealing near the exothermic peak temperature presents the best enhancing effect on the semi-hard magnetic property of FeSiBAlNiCo. It performs both large saturated magnetization and remanence ratio of 13.0 emu/g and near 45%, which exhibit 465% and 105% enhancement compared with as-milled state, respectively. - Highlights: • Co, Cu, Ag additions affect crystallization behavior of FeSiBAlNi amorphous HEAs. • Crystallization products in FeSiBAlNi Co/Ag reveal high phase stability. • Proper FeSi-rich and FeB-rich phases are beneficial to improve magnetic property. • Annealing treatment improves semi-hard magnetic property compared to as-milled state. • Annealing near exothermic peak temperature shows best enhancing effect on magnetism.

Comparative study of transparent ceramic and single crystal Ce doped LuAG scintillators

International Nuclear Information System (INIS)

Yanagida, Takayuki; Fujimoto, Yutaka; Yokota, Yuui; Kamada, Kei; Yanagida, Satoko; Yoshikawa, Akira; Yagi, Hideki; Yanagitani, Takagimi

2011-01-01

Transparent ceramic Ce 0.5% doped Lu 3 Al 5 O 12 (LuAG) scintillator grown by the sintering method and single crystalline Ce doped LuAG grown by the Czochralski method are prepared. They are cut to the physical dimensions 4 × 4 × 2 mm 3 . Their transmittance and radio luminescence spectra are evaluated. They are both transmissive in wavelength longer than 500 nm and intense Ce 3+ 5d–4f emission appears around 520 nm. When 137 Cs γ-ray is irradiated, 662 keV photo-absorption peaks are clearly observed in each sample. The transparent ceramic one shows higher light yield than that of the single crystalline one. The absolute light yield of the ceramic sample is turned out to be 14800 ± 1500 ph/MeV. The decay time constants are evaluated under pulse X-ray excitation. The main component of the decay time of ceramic and single crystalline one are determined as 37 and 46 ns, respectively.

Studies on the effect of AgNP binding on α-amylase structure of porcine pancreas and Bacillus subtilis by multi-spectroscopic methods

International Nuclear Information System (INIS)

Ernest, Vinita; Sekar, Gajalakshmi; Mukherjee, Amitava; Chandrasekaran, N.

2014-01-01

Functionalizing silver nanoparticles (AgNPs) with biomolecules have a number of applications in catalysis, sensing, pharmaceutics and therapy. For the first time, herein we report the interaction of amylase-AgNPs through various spectroscopic techniques. AgNPs are synthesized and characterized by UV–vis spectroscopy, transmission electron microscopy (TEM) and Dynamic Light Scattering (DLS). The binding of AgNPs to α-amylase are investigated by UV–vis, fluorescence, circular dichroism and FTIR spectroscopic techniques. Absorption intensity and Stern–Volmer plots confirmed the formation of the ground state complex with AgNPs. The quenching of the intrinsic protein fluorescence in the presence of different concentrations of AgNP was observed. The apparent binding constant (K) and number of binding sites (n) was calculated from the Stern–Volmer plot was found to be 4.92×10 3 , 3.8×10 3 and 1.57, 1.3 for porcine pancreas and Bacillus subtilis α-amylase, respectively. Far-UV CD studies revealed the characteristic dichoric band at 222 nm for α-helical structure was shifted to 215 nm in porcine pancreatic α-amylase upon AgNP binding. Further, structural conformation change with peak shifts and the possible binding residues was confirmed through FTIR spectroscopy. -- Highlights: • AgNPs were synthesized using modified Creighton's method and characterized. • Structural changes analyzed by UV–vis, fluorescence spectroscopy. • CD and FTIR spectra reveal the secondary structure conformation change. • Potential application in food industry

Studies on the effect of AgNP binding on α-amylase structure of porcine pancreas and Bacillus subtilis by multi-spectroscopic methods

Energy Technology Data Exchange (ETDEWEB)

Ernest, Vinita; Sekar, Gajalakshmi; Mukherjee, Amitava; Chandrasekaran, N., E-mail: nchandrasekaran@vit.ac.in

2014-02-15

Functionalizing silver nanoparticles (AgNPs) with biomolecules have a number of applications in catalysis, sensing, pharmaceutics and therapy. For the first time, herein we report the interaction of amylase-AgNPs through various spectroscopic techniques. AgNPs are synthesized and characterized by UV–vis spectroscopy, transmission electron microscopy (TEM) and Dynamic Light Scattering (DLS). The binding of AgNPs to α-amylase are investigated by UV–vis, fluorescence, circular dichroism and FTIR spectroscopic techniques. Absorption intensity and Stern–Volmer plots confirmed the formation of the ground state complex with AgNPs. The quenching of the intrinsic protein fluorescence in the presence of different concentrations of AgNP was observed. The apparent binding constant (K) and number of binding sites (n) was calculated from the Stern–Volmer plot was found to be 4.92×10{sup 3}, 3.8×10{sup 3} and 1.57, 1.3 for porcine pancreas and Bacillus subtilis α-amylase, respectively. Far-UV CD studies revealed the characteristic dichoric band at 222 nm for α-helical structure was shifted to 215 nm in porcine pancreatic α-amylase upon AgNP binding. Further, structural conformation change with peak shifts and the possible binding residues was confirmed through FTIR spectroscopy. -- Highlights: • AgNPs were synthesized using modified Creighton's method and characterized. • Structural changes analyzed by UV–vis, fluorescence spectroscopy. • CD and FTIR spectra reveal the secondary structure conformation change. • Potential application in food industry.

Both released silver ions and particulate Ag contribute to the toxicity of AgNPs to earthworm Eisenia fetida

NARCIS (Netherlands)

Li, L.; , van, Gestel C.A.M.

2015-01-01

To disentangle the contribution of ionic and nanoparticulate Ag to the overall toxicity to the earthworm Eisenia fetida, a semi-permeable membrane strategy was used to separate Ag+ released from silver nanoparticles (AgNPs) in an aqueous exposure. Internal Ag fractionation, activities of antioxidant

[Ag67(SPhMe2)32(PPh3)8]3+: Synthesis, Total Structure, and Optical Properties of a Large Box-Shaped Silver Nanocluster

KAUST Repository

Alhilaly, Mohammad J.; Bootharaju, Megalamane Siddaramappa; Joshi, Chakra Prasad; Besong, Tabot M.D.; Emwas, Abdul-Hamid M.; Juarez-Mosqueda, Rosalba; Kaappa, Sami; Malola, Sami; Adil, Karim; Shkurenko, Aleksander; Hakkinen, Hannu; Eddaoudi, Mohamed; Bakr, Osman

2016-01-01

Engineering the surface ligands of metal nanoparticles is critical in designing unique arrangements of metal atoms. Here, we report the synthesis and total structure determination of a large box-shaped Ag-67 nanocluster (NC) protected by a mixed shell of thiolate (2,4-dimethylbenzenethiolate, SPhMe2) and phosphine (triphenylphosphine, PPh3) ligands. Single crystal X-ray diffraction (SCXRD) and electrospray ionization mass spectrometry (ESI-MS) revealed the cluster formula to be [Ag-67(SPhMe2)(32)(PPh3)(8)](3+). The crystal structure shows an Ag-23 metal core covered by a layer of Ag44S32P8 arranged in the shape of a box. The Ag-13, core was formed through an unprecedented centered cuboctahedron, i.e., Ag-13, unlike the common centered Ag-13 icosahedron geometry. Two types of ligand motifs, eight AgS3P and eight bridging thiols, were found to stabilize the whole cluster. The optical spectrum of this NC displayed highly structured multiple absorption peaks. The electronic structure and optical spectrum of Ag-67 were computed using time-dependent density functional theory (TDDFT) for both the full cluster [Ag-67(SPhMe2)(32)(PPh3)(8)](3+) and a reduced model [Ag-67(SH)(32)(PH3)(8)](3+). The lowest metal-to-metal transitions in the range 500-800 nm could be explained by considering the reduced model that shows almost identical electronic states to 32 free electrons in a jellium box. The successful synthesis of the large box-shaped Ag-67 NC facilitated by the combined use of phosphine and thiol paves the way for synthesizing other metal clusters with unprecedented shapes by judicious choice of thiols and phosphines.

[Ag67(SPhMe2)32(PPh3)8]3+: Synthesis, Total Structure, and Optical Properties of a Large Box-Shaped Silver Nanocluster

KAUST Repository

Alhilaly, Mohammad J.

2016-10-13

Engineering the surface ligands of metal nanoparticles is critical in designing unique arrangements of metal atoms. Here, we report the synthesis and total structure determination of a large box-shaped Ag-67 nanocluster (NC) protected by a mixed shell of thiolate (2,4-dimethylbenzenethiolate, SPhMe2) and phosphine (triphenylphosphine, PPh3) ligands. Single crystal X-ray diffraction (SCXRD) and electrospray ionization mass spectrometry (ESI-MS) revealed the cluster formula to be [Ag-67(SPhMe2)(32)(PPh3)(8)](3+). The crystal structure shows an Ag-23 metal core covered by a layer of Ag44S32P8 arranged in the shape of a box. The Ag-13, core was formed through an unprecedented centered cuboctahedron, i.e., Ag-13, unlike the common centered Ag-13 icosahedron geometry. Two types of ligand motifs, eight AgS3P and eight bridging thiols, were found to stabilize the whole cluster. The optical spectrum of this NC displayed highly structured multiple absorption peaks. The electronic structure and optical spectrum of Ag-67 were computed using time-dependent density functional theory (TDDFT) for both the full cluster [Ag-67(SPhMe2)(32)(PPh3)(8)](3+) and a reduced model [Ag-67(SH)(32)(PH3)(8)](3+). The lowest metal-to-metal transitions in the range 500-800 nm could be explained by considering the reduced model that shows almost identical electronic states to 32 free electrons in a jellium box. The successful synthesis of the large box-shaped Ag-67 NC facilitated by the combined use of phosphine and thiol paves the way for synthesizing other metal clusters with unprecedented shapes by judicious choice of thiols and phosphines.

Quantitative HBsAg and HBeAg predict hepatitis B seroconversion after initiation of HAART in HIV-HBV coinfected individuals.

Directory of Open Access Journals (Sweden)

Gail V Matthews

Full Text Available OBJECTIVE: Anti-HBe seroconversion and HBsAg loss are important therapeutic endpoints in patients with hepatitis B virus (HBV infection. Quantitative measures of hepatitis B surface antigen (qHBsAg and e antigen (qHBeAg have been identified as potentially useful indicators of therapeutic response in HBV monoinfection. The aim of this study was to examine serological change including quantitative biomarkers in HIV-HBV coinfected patients initiating HBV active antiretroviral therapy (ART. METHODS: HIV-HBV coinfected individuals from Thailand were followed for up to 168 weeks post ART. Rates and associations of qualitative serological change were determined. Longitudinal changes in qHBsAg and qHBeAg were measured and their utility as predictors of response examined. RESULTS: Forty seven patients were included of whom 27 (57% were HBeAg positive at baseline. Median CD4 count was 48 cells/mm(3. Over a median follow-up of 108 weeks 48% (13/27 lost HBeAg, 12/27 (44% achieved anti-HBe seroconversion and 13% (6/47 HBsAg loss. Anti-HBe seroconversion was associated with higher baseline ALT (p = 0.034, lower qHBsAg (p = 0.015, lower qHBeAg (p = 0.031 and greater HBV DNA decline to week 24 (p = 0.045. Sensitivity and specificity for qHBsAg and qHBeAg decline of >0.5 log at week 12 and >1.0 log at week 24 were high for both anti-HBe seroconversion and HBsAg loss. CONCLUSIONS: Rates of serological change in these HIV-HBV coinfected individuals with advanced immunodeficiency initiating HBV-active ART were high. Baseline and on treatment factors were identified that were associated with a greater likelihood of subsequent anti-HBe seroconversion, including both quantitative HBsAg and HBeAg, suggesting these biomarkers may have utility in this clinical setting.

One-pot solvothermal synthesis of highly efficient, daylight active and recyclable Ag/AgBr coupled photocatalysts with synergistic dual photoexcitation

International Nuclear Information System (INIS)

Zhang, Caihong; Ai, Lunhong; Li, Lili; Jiang, Jing

2014-01-01

Highlights: • Ag/AgBr photocatalysts were controllably synthesized by solvothermal process. • Ag/AgBr composites showed excellent daylight driven photocatalytic activity. • The remarkable activity is attributed to the synergistic dual photoexcitation. -- Abstract: Efficient light harvesting has been considered to be critical for manipulating the photocatalytic behavior of photocatalysts, because it directly determines the generation of reactive redox charge carriers involved in photoreaction process. In this study, we present a successful example on efficient conversion of solar energy by Ag/AgBr coupled photocatalysts that hold unique synergistic dual photoexcitation. A series of Ag/AgBr coupled photocatalysts were controllably synthesized by an easily manipulated mild solvothermal process. The physicochemical properties of the as-prepared Ag/AgBr coupled photocatalysts were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray energy dispersive spectroscopy (EDS) and UV–vis diffuse reflectance spectroscopy (DRS). The results showed the solvothermal reaction time played key role for control of crystalline structure, morphology, composition, and visible light absorption ability of the resulting photocatalysts. The as-prepared Ag/AgBr coupled photocatalysts exhibited remarkable photocatalytic performance and good reusability for decomposing organic dyes in aqueous solution under the irradiation of commercial 20 W cool daylight fluorescent lamp, owing to the synergistic dual photoexcitation cooperating between plasmonic Ag nanoparticles and narrow-band-gap AgBr

Preparation and thermomechanical properties of Ag-PVA nanocomposite films

International Nuclear Information System (INIS)

Gautam, Anurag; Ram, S.

2010-01-01

Metal-polymer hybrid nanocomposites have been prepared from an aqueous solution of polyvinyl alcohol (PVA) and silver nitrate (AgNO 3 ). The silver nanoparticles were generated in PVA matrix by the reduction of silver ions with PVA molecule at 60-70 deg. C over magnetic stirrer. UV-vis analysis, X-ray diffraction studies, transmission electron microscopy, scanning electron microscopy and current-voltage analysis were used to characterize the nanocomposite films prepared. The X-ray diffraction analysis reveals that silver metal is present in face centered cubic (fcc) crystal structure. Average crystallite size of silver nanocrystal is 19 nm, which increases to 22 nm on annealing the film at 150 deg. C in air. This result is in good agreement with the result obtained from TEM. The UV-vis spectrum shows a single peak at 433 nm, arising from the surface plasmon absorption of silver nanocolloids. This result clearly indicates that silver nanoparticles are embedded in PVA. An improvement of mechanical properties (storage modulus) was also noticed due to a modification of PVA up to 0.5 wt% of silver content. The current-voltage (I-V) characteristic of nanocomposite films shows increase in current drawn with increasing Ag-content in the films.

AGS experiments: 1990, 1991, 1992

International Nuclear Information System (INIS)

Depken, J.C.

1993-04-01

This report contains a description of the following: AGS Experimental Area - High Energy Physics FY 1993 and Heavy Ion Physics FY 1993; Table of Beam Parameters and Fluxes; Experiment Schedule ''as run''; Proposed 1993 Schedule; A listing of experiments by number; Two-page summaries of each experiment begin here, also ordered by number; Publications of AGS Experiments; and List of AGS Experimenters

Short-Term Biliary Stent Placement Contributing Common Bile Duct Stone Disappearance with Preservation of Duodenal Papilla Function

Directory of Open Access Journals (Sweden)

Tatsuki Ueda

2016-01-01

Full Text Available Aims. To investigate the effect of biliary stent placement without endoscopic sphincterotomy (EST on common bile duct stones (CBDS disappearance and the contribution of preserving the duodenal papilla function to reduce recurrence of CBDS. Methods. Sixty-six patients admitted for acute obstructive cholangitis due to CBDS who underwent biliary stent placement without EST for 2 years from March 2011 were evaluated retrospectively. The second endoscopic retrograde cholangiopancreatography (ERCP was performed for treatment of CBDS 3 to 4 months after the first ERCP. We estimated the rate of stone disappearance at the time of second ERCP. Results. CBDS disappearance was observed in 32 (48.5% of 66 patients. The diameter of the bile ducts and the diameter of CBDS in patients with CBDS disappearance were significantly smaller than in those with CBDS requiring extraction (p=0.007 and p<0.001, resp.. Stone disappearance was evident when the diameter of bile ducts and that of CBDS were <10 and 7 mm, respectively (p=0.002. Conclusions. Short-term stent placement without EST eliminates CBDS while preserving duodenal papilla function and may be suitable for treating CBDS in patients with nondilated bile ducts and small CBDS.

Influence of the surface properties on bactericidal and fungicidal activity of magnetron sputtered Ti–Ag and Nb–Ag thin films

Energy Technology Data Exchange (ETDEWEB)

Wojcieszak, D., E-mail: damian.wojcieszak@pwr.edu.pl [Faculty of Microsystem Electronics and Photonics, Wroclaw University of Technology, Janiszewskiego 11/17, 50-372 Wrocław (Poland); Mazur, M.; Kaczmarek, D. [Faculty of Microsystem Electronics and Photonics, Wroclaw University of Technology, Janiszewskiego 11/17, 50-372 Wrocław (Poland); Mazur, P. [Institute of Experimental Physics, University of Wrocław, Max Born 9, 50-204 Wrocław (Poland); Szponar, B. [Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Rudolfa Weigla 12, 53–114 Wrocław (Poland); Domaradzki, J. [Faculty of Microsystem Electronics and Photonics, Wroclaw University of Technology, Janiszewskiego 11/17, 50-372 Wrocław (Poland); Kepinski, L. [Institute of Low Temperature and Structure Research, Polish Academy of Sciences, Okólna 2, 50-422 Wrocław (Poland)

2016-05-01

In this study the comparative investigations of structural, surface and bactericidal properties of Ti–Ag and Nb–Ag thin films have been carried out. Ti–Ag and Nb–Ag coatings were deposited on silicon and fused silica substrates by magnetron co-sputtering method using innovative multi-target apparatus. The physicochemical properties of prepared thin films were examined with the aid of X-ray diffraction, grazing incidence X-ray diffraction, scanning electron microscopy, atomic force microscopy and X-ray photoelectron spectroscopy methods. Moreover, the wettability of the surface was determined. It was found that both, Ti–Ag and Nb–Ag thin films were nanocrystalline. In the case of Ag–Ti film presence of AgTi{sub 3} and Ag phases was identified, while in the structure of Nb–Ag only silver occurred in a crystal form. In both cases the average size of crystallites was ca. 11 nm. Moreover, according to scanning electron microscopy and atomic force microscopy investigations the surface of Nb–Ag thin films was covered with Ag-agglomerates, while Ti–Ag surface was smooth and devoid of silver particles. Studies of biological activity of deposited coatings in contact with Bacillus subtilis, Pseudomonas aeruginosa, Enterococcus hirae, Klebisiella pneumoniae, Escherichia coli, Staphylococcus aureus and Candida albicans were performed. It was found that prepared coatings were bactericidal and fungicidal even in a short term-contact, i.e. after 2 h. - Highlights: • Surface and biological properties of Ti–Ag and Nb–Ag thin films were examined. • Ag content was related to sputtering yields and nucleation of Ti and Nb. • For Nb–Ag film the agglomeration of silver at the surface was observed. • Composition and surface topography had an impact on antimicrobial properties. • Fine-grained surface was important in Ag ions release process.

Influence of the surface properties on bactericidal and fungicidal activity of magnetron sputtered Ti–Ag and Nb–Ag thin films

International Nuclear Information System (INIS)

Wojcieszak, D.; Mazur, M.; Kaczmarek, D.; Mazur, P.; Szponar, B.; Domaradzki, J.; Kepinski, L.

2016-01-01

In this study the comparative investigations of structural, surface and bactericidal properties of Ti–Ag and Nb–Ag thin films have been carried out. Ti–Ag and Nb–Ag coatings were deposited on silicon and fused silica substrates by magnetron co-sputtering method using innovative multi-target apparatus. The physicochemical properties of prepared thin films were examined with the aid of X-ray diffraction, grazing incidence X-ray diffraction, scanning electron microscopy, atomic force microscopy and X-ray photoelectron spectroscopy methods. Moreover, the wettability of the surface was determined. It was found that both, Ti–Ag and Nb–Ag thin films were nanocrystalline. In the case of Ag–Ti film presence of AgTi_3 and Ag phases was identified, while in the structure of Nb–Ag only silver occurred in a crystal form. In both cases the average size of crystallites was ca. 11 nm. Moreover, according to scanning electron microscopy and atomic force microscopy investigations the surface of Nb–Ag thin films was covered with Ag-agglomerates, while Ti–Ag surface was smooth and devoid of silver particles. Studies of biological activity of deposited coatings in contact with Bacillus subtilis, Pseudomonas aeruginosa, Enterococcus hirae, Klebisiella pneumoniae, Escherichia coli, Staphylococcus aureus and Candida albicans were performed. It was found that prepared coatings were bactericidal and fungicidal even in a short term-contact, i.e. after 2 h. - Highlights: • Surface and biological properties of Ti–Ag and Nb–Ag thin films were examined. • Ag content was related to sputtering yields and nucleation of Ti and Nb. • For Nb–Ag film the agglomeration of silver at the surface was observed. • Composition and surface topography had an impact on antimicrobial properties. • Fine-grained surface was important in Ag ions release process.

Quantitative optical extinction-based parametric method for sizing a single core-shell Ag-Ag{sub 2}O nanoparticle

Energy Technology Data Exchange (ETDEWEB)

Santillan, J M J; Scaffardi, L B; Schinca, D C, E-mail: lucias@ciop.unlp.edu.ar [Centro de Investigaciones Opticas (CIOp), (CONICET La Plata-CIC) (Argentina)

2011-03-16

This paper develops a parametric method for determining the core radius and shell thickness in small silver-silver-oxide core-shell nanoparticles (Nps) based on single particle optical extinction spectroscopy. The method is based on the study of the relationship between plasmon peak wavelength, full width at half maximum (FWHM) and contrast of the extinction spectra as a function of core radius and shell thickness. This study reveals that plasmon peak wavelength is strongly dependent on shell thickness, whereas FWHM and contrast depend on both variables. These characteristics may be used for establishing an easy and fast stepwise procedure to size core-shell NPs from single particle absorption spectrum. The importance of the method lies in the possibility of monitoring the growth of the silver-oxide layer around small spherical silver Nps in real time. Using the electrostatic approximation of Mie theory, core-shell single particle extinction spectra were calculated for a silver particle's core size smaller than about 20 nm and different thicknesses of silver oxide around it. Analysis of the obtained curves shows a very particular characteristic of the plasmon peak of small silver-silver-oxide Nps, expressed in the fact that its position is strongly dependent on oxide thickness and weakly dependent on the core radius. Even a very thin oxide layer shifts the plasmon peak noticeably, enabling plasmon tuning with appropriate shell thickness. This characteristic, together with the behaviour of FWHM and contrast of the extinction spectra can be combined into a parametric method for sizing both core and shell of single silver Nps in a medium using only optical information. In turn, shell thickness can be related to oxygen content in the Np's surrounding media. The method proposed is applied to size silver Nps from single particle extinction spectrum. The results are compared with full optical spectrum fitting using the electrostatic approximation in Mie theory

Synthesis of β-AgVO3 nanowires decorated with Ag2CrO4, with improved visible light photocatalytic performance

Science.gov (United States)

Ouyang, Qi; Li, Zhonghua; Liu, Jiawen

2018-05-01

Silver chromate‑silver vanadate (Ag2CrO4/β-AgVO3) heterojunction composites are synthesized through a facile precipitation process. The Ag2CrO4/β-AgVO3 hybrids obtained exhibit better photocatalytic activity in degradation of RhB than both pure Ag2CrO4 and β-AgVO3 under visible light irradiation. The 20 wt% Ag2CrO4/β-AgVO3 heterojunction possesses the best photocatalytic ability for degrading RhB: 24.4 times that of pristine β-AgVO3 nanowires and 3.2 times that of individual Ag2CrO4 particles. The phase of the nanocomposites was analyzed using x-ray diffraction as well as x-ray photoelectron spectroscopy. Their morphology was observed via scanning electron microscopy and transmission electron microscopy. The improvement in photocatalytic performance is chiefly ascribed to the synergies between Ag2CrO4/β-AgVO3 heterostructure, which can enhance the light absorbance ability and also accelerate the separation and transfer of photoinduced electrons and holes under visible light irradiation; this is also confirmed by UV–vis diffuse reflection spectrometry and fluorescence emission spectra.