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Sample records for light po isotopes

  1. Properties of Light Hg, Pb and Po Isotopes

    CERN Document Server

    Muntian, I

    2003-01-01

    Quality of mass description for three different theoretical mass models is studied. Masses and deformations for Po, Pb and Hg isotopes are compared with experimental data. Gap in the proton single particle energy spectrum is discussed.

  2. The influence of intruder states in even-even Po isotopes

    Energy Technology Data Exchange (ETDEWEB)

    García-Ramos, J. E., E-mail: enrique.ramos@dfaie.uhu.es [Departamento de Física Aplicada, Universidad de Huelva, 21071 Huelva (Spain); Heyde, K., E-mail: kris.heyde@ugent.be [Department of Physics and Astronomy, Ghent University, Proeftuinstraat 86, B-9000 Gent (Belgium)

    2015-10-15

    We study the role of intruder states and shape coexistence in the even-even {sup 190–206}Po isotopes, through an interacting boson model with configuration mixing calculation. We analyzed the results in the light of known systematics on various observable in the Pb region, paying special attention to the unperturbed energy systematics and quadrupole deformation. We find that shape coexistence in the Po isotopes behaves in very much the same way as in the Pt isotopes, i.e., it is somehow hidden, contrary to the situation in the Pb and the Hg isotopes.

  3. Graphs for Isotopes of 84-Po(Polonium)

    Science.gov (United States)

    Sukhoruchkin, S. I.; Soroko, Z. N.

    This document is part of the Supplement containing the complete sets of data of Subvolume B `Nuclei with Z = 55 - 100' of Volume 22 `Nuclear Binding Energies and Atomic Masses' of Landolt-Börnstein - Group I `Elementary Particles, Nuclei and Atoms', and additionally including data for nuclei with Z = 101 - 130. It provides a graphic representation of nucleon separation energies and residual interaction parameters for isotopes of the chemical element 84-Po (Polonium, atomic number Z = 84).

  4. Shell model description of low-lying states in Po and Rn isotopes

    Science.gov (United States)

    Higashiyama, Koji; Yoshinaga, Naotaka

    2014-03-01

    Nuclear structure of the Po and Rn isotopes is theoretically studied in terms of the spherical shell model with the monopole- and quadrupole-pairing plus quadrupole-quadrupole effective interaction. The experimental energy levels of low-lying states are well reproduced. The shell model results are examined in detail in a pair-truncated shell model. The analysis reveals the alignment of two protons in the 0h9/2 orbital at spin 8.

  5. Shell model description of low-lying states in Po and Rn isotopes

    Directory of Open Access Journals (Sweden)

    Higashiyama Koji

    2014-03-01

    Full Text Available Nuclear structure of the Po and Rn isotopes is theoretically studied in terms of the spherical shell model with the monopole- and quadrupole-pairing plus quadrupole-quadrupole effective interaction. The experimental energy levels of low-lying states are well reproduced. The shell model results are examined in detail in a pair-truncated shell model. The analysis reveals the alignment of two protons in the 0h9/2 orbital at spin 8.

  6. Study of quadrupole collectivity in odd mass Po and Bi isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Pai, H.; Reese, M.; Pietralla, N. [Institut fuer Kernphysik, Technische Universitaet Darmstadt, D-64289 Darmstadt (Germany); Cortes, M.L. [Institut fuer Kernphysik, Technische Universitaet Darmstadt, D-64289 Darmstadt (Germany); GSI Helmholtzzentrum fuer Schwerionenforschung GmbH, D-64291 Darmstadt (Germany); Gerl, J.; Gorska, M. [GSI Helmholtzzentrum fuer Schwerionenforschung GmbH, D-64291 Darmstadt (Germany); Podolyak, Zs. [Department of Physics, University of Surrey, Guildford, GU2 7XH (United Kingdom); Rudolph, D. [Department of Physics, Lund University, SE-22100 Lund (Sweden); Collaboration: S429 PreSPEC-AGATA-Collaboration

    2015-07-01

    Relativistic Coulomb excitations of odd-mass Po and Bi isotopes were performed during the PreSPEC-AGATA campaign at GSI to study the quadrupole collectivity in the direct vicinity of the heaviest stable doubly-magic nucleus {sup 208}Pb. The PreSPEC-AGATA campaign is the predecessor of the HISPEC (High-resolution In-flight Spectroscopy) experiment in the FAIR context. It was running 2012 and 2014 at GSI. Up to 23 AGATA crystals were used in this campaign, located behind the FRagment Separator. We present the status of the ongoing data analysis and discuss the challenges of data analysis for this type of experiments.

  7. Visible light assisted degradation of organic dye using Ag{sub 3}PO{sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Dhanabal, R.; Bose, A. Chandra, E-mail: acbose@nitt.edu [Nanomaterials Laboratory, Department of Physics, National Institute of Technology Tiruchirappalli – 620 015 India (India); Velmathi, S. [Organic and Polymer Synthesis Laboratory, Department of Chemistry, National Institute of Technology Tiruchirappalli – 620 015 India (India)

    2015-06-24

    The study of visible light photodegradation of organic dye Methylene Blue (MB) have been investigated using silver phosphate (Ag{sub 3}PO{sub 4}) as a photocatalyst which is good efficient material for photocatalytic reaction. The simple ion-exchange method is used to prepare Ag{sub 3}PO{sub 4}. The structure of the material have been confirmed using X-ray diffraction which shows cubic structure of Ag{sub 3}PO{sub 4}. The functional group of the Ag{sub 3}PO{sub 4} has been verified by Fourier transform infrared spectroscopy. The bandgap of Ag{sub 3}PO{sub 4} is calculated using kubelka-munk function from the ultra violet-visible diffuse reflectance spectroscopy, the absorption of Ag{sub 3}PO{sub 4} starts from 470 nm. Under simulated visible light irradiation, Ag{sub 3}PO{sub 4} catalyst exhibits good catalytic ability for degrading MB dye.

  8. Probing the metabolic water contribution to intracellular water using oxygen isotope ratios of PO4

    Science.gov (United States)

    Li, Hui; Yu, Chan; Wang, Fei; Chang, Sae Jung; Yao, Jun; Blake, Ruth E.

    2016-05-01

    Knowledge of the relative contributions of different water sources to intracellular fluids and body water is important for many fields of study, ranging from animal physiology to paleoclimate. The intracellular fluid environment of cells is challenging to study due to the difficulties of accessing and sampling the contents of intact cells. Previous studies of multicelled organisms, mostly mammals, have estimated body water composition—including metabolic water produced as a byproduct of metabolism—based on indirect measurements of fluids averaged over the whole organism (e.g., blood) combined with modeling calculations. In microbial cells and aquatic organisms, metabolic water is not generally considered to be a significant component of intracellular water, due to the assumed unimpeded diffusion of water across cell membranes. Here we show that the 18O/16O ratio of PO4 in intracellular biomolecules (e.g., DNA) directly reflects the O isotopic composition of intracellular water and thus may serve as a probe allowing direct sampling of the intracellular environment. We present two independent lines of evidence showing a significant contribution of metabolic water to the intracellular water of three environmentally diverse strains of bacteria. Our results indicate that ˜30-40% of O in PO4 comprising DNA/biomass in early stationary phase cells is derived from metabolic water, which bolsters previous results and also further suggests a constant metabolic water value for cells grown under similar conditions. These results suggest that previous studies assuming identical isotopic compositions for intracellular/extracellular water may need to be reconsidered.

  9. Radioactivity of cigarettes and the importance of (210)Po and thorium isotopes for radiation dose assessment due to smoking.

    Science.gov (United States)

    Kubalek, Davor; Serša, Gregor; Štrok, Marko; Benedik, Ljudmila; Jeran, Zvonka

    2016-05-01

    Tobacco and tobacco smoke are very complex mixtures. In addition to various chemical and organic compounds they also contain natural radioactive elements (radionuclides). In this work, the natural radionuclide activity concentrations ((234)U, (238)U, (228)Th, (230)Th, (232)Th, (226)Ra, (210)Pb and (210)Po) of nine different cigarette samples available on the Slovenian market are reported. In addition to (210)Po, the transfer of thorium isotopes from a cigarette to a smoker's body and lungs have been determined for the first time. Cigarette smoke and exhaled air from smokers' lungs were collected from volunteer smokers (C-4 brand) to determinate what quantity of (210)Po and thorium isotopes is transferred from the tobacco to the smoker's lungs. Cigarette ash and smoked filters were also collected and analysed. Among the determined isotopes, (210)Pb and (210)Po showed the highest activity concentrations. During the smoking of one cigarette approximately 22% of (210)Po (and presumably its predecessor (210)Pb), 0.6% of (228)Th, 24% of (230)Th, and 31% of (232)Th are transferred from the cigarette and retained in the smoker's body. The estimated annual effective dose for smokers is 61 μSv/year from (210)Po; 9 μSv/year from (210)Pb; 6 μSv/year from (228)Th; 47 μSv/year from (230)Th, and 37 μSv/year from (232)Th. These results show the importance of thorium isotopes in contributing to the annual effective dose for smoking. Copyright © 2016 Elsevier Ltd. All rights reserved.

  10. Hydroxyapatite supported Ag3PO4 nanoparticles with higher visible light photocatalytic activity

    Science.gov (United States)

    Hong, Xiaoting; Wu, Xiaohui; Zhang, Qiuyun; Xiao, Mingfeng; Yang, Gelin; Qiu, Meirong; Han, Guocheng

    2012-03-01

    Hydroxyapatite supported Ag3PO4 nanocomposites have been synthesized by a wet impregnation process. UV-vis absorption spectra show a red shift of the absorption edges for the composite systems compared to pure hydroxyapatite support. The surface structure and morphology of the nanocomposites were characterized by Brunauer-Emmett-Teller (BET) apparatus, X-ray diffraction (XRD), transmission electron microscopy (TEM). The results suggest that Ag3PO4 nanoparticles (6-17 nm in diameter) are well dispersed on the hydroxyapatite support and Ag3PO4 nanoparticles density is larger for the higher Ag+ loading sample. The as-prepared nanocomposite photocatalysts showed a pronounced photocatalytic activity upon decomposition of methylene blue dye in aqueous solution under both visible light (wavelength > 400 nm) and UV-vis light irradiation. A synergic mechanism of inherent photocatalytic capability of Ag3PO4 and the accelerated electron/hole separation resulting from the photoinduced electrons captured by the slow-released Ag+ at the interface of Ag3PO4 and hydroxyapatite is proposed for the nanocomposites on the enhancement of photocatalytic performance in comparison to that of pure Ag3PO4 nanoparticles. The support of hydroxyapatite may also act as an absorbent which favors the mass transfer in heterogeneous photocatalysis reaction.

  11. UV-light driven photocatalytic performance of hydrothermally-synthesized hexagonal CePO4 nanorods

    Science.gov (United States)

    Zhu, Zhongqi; Zhang, Ke; Zhao, Heyun; Zhu, Jing

    2017-10-01

    Hexagonal CePO4 nanorods were synthesized via a simple hydrothermal method without the presence of surfactants and then characterized by powder X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), ultraviolet-visible (UV-vis) absorption and photoluminescence (PL) spectroscopy. UV-light driven photocatalytic activities of hexagonal CePO4 nanorods were detailedly demonstrated via degrading different organic dyes such as congo red (CR), organic rhodamine B (RB), methyl orange (MO) and methylene blue (MB) since these nanorods exhibit strong UV absorption with the cutoff edge of about 420 nm.

  12. HELIX: The High Energy Light Isotope Experiment

    Science.gov (United States)

    Wakely, Scott

    This is the lead proposal for a new suborbital program, HELIX (High-Energy Light Isotope eXperiment), designed to make measurements of the isotopic composition of light cosmic-ray nuclei from ~200 MeV/nuc to ~10 GeV/nuc. Past measurements of this kind have provided profound insights into the nature and origin of cosmic rays, revealing, for instance, information on acceleration and confinement time scales, and exposing some conspicuous discrepancies between solar and cosmic-ray abundances. The most detailed information currently available comes from the ACE/CRIS mission, but is restricted to energies below a few 100 MeV/nuc. HELIX aims at extending this energy range by over an order of magnitude, where, in most cases, no measurements of any kind exist, and where relativistic time dilation affects the apparent lifetime of radioactive clock nuclei. The HELIX measurements will provide essential information for understanding the propagation history of cosmic rays in the galaxy. This is crucial for properly interpreting several intriguing anomalies reported in recent cosmic-ray measurements, pertaining to the energy spectra of protons, helium, and heavier nuclei, and to the anomalous rise in the positron fraction at higher energy. HELIX employs a high-precision magnet spectrometer to provide measurements which are not achievable by any current or planned instrument. The superconducting magnet originally used for the HEAT payload in five successful high-altitude flights will be combined with state-of-the-art detectors to measure the charge, time-of-flight, magnetic rigidity, and velocity of cosmic-ray particles with high precision. The instrumentation includes plastic scintillators, silicon-strip detectors repurposed from Fermilab's CDF detector, a high-performance gas drift chamber, and a ring-imaging Cherenkov counter employing aerogel radiators and silicon photomultipliers. To reduce cost and technical risk, the HELIX program will be structured in two stages. The first

  13. Heterostructured Ag3PO4/AgBr/Ag plasmonic photocatalyst with enhanced photocatalytic activity and stability under visible light

    Science.gov (United States)

    Wang, Wan-Sheng; Du, Hong; Wang, Rui-Xia; Wen, Tao; Xu, An-Wu

    2013-03-01

    A heterostructured Ag3PO4/AgBr/Ag plasmonic photocatalyst was prepared by a rational in situ ion exchange reaction between Ag3PO4 micro-cubes and Br- in aqueous solution followed by photoreduction. The photocatalytic activities of obtained photocatalysts were measured by the degradation of methyl orange (MO) and methylene blue (MB) under visible light irradiation (λ >= 400 nm). Compared to AgBr/Ag, Ag3PO4/AgBr heterocrystals and pure Ag3PO4 crystals, the heterostructured Ag3PO4/AgBr/Ag plasmonic photocatalysts exhibit much higher photocatalytic activity and stability. This enhanced photocatalytic activity suggests that the synergetic effects of the heterostructured Ag3PO4/AgBr/Ag and the strong SPR of Ag NPs on the surface result in the high efficiencies of the photocatalytic activity and the improved stability. With the assistance of Ag3PO4/AgBr/Ag heterostructures, only 8 min and 12 min are taken to completely decompose MO and MB molecules under visible-light irradiation, respectively. Furthermore, the photodegradation rate does not show an obvious decrease during ten successive cycles, indicating that our heterostructured Ag3PO4/AgBr/Ag plasmonic photocatalysts are extremely stable under visible-light irradiation.A heterostructured Ag3PO4/AgBr/Ag plasmonic photocatalyst was prepared by a rational in situ ion exchange reaction between Ag3PO4 micro-cubes and Br- in aqueous solution followed by photoreduction. The photocatalytic activities of obtained photocatalysts were measured by the degradation of methyl orange (MO) and methylene blue (MB) under visible light irradiation (λ >= 400 nm). Compared to AgBr/Ag, Ag3PO4/AgBr heterocrystals and pure Ag3PO4 crystals, the heterostructured Ag3PO4/AgBr/Ag plasmonic photocatalysts exhibit much higher photocatalytic activity and stability. This enhanced photocatalytic activity suggests that the synergetic effects of the heterostructured Ag3PO4/AgBr/Ag and the strong SPR of Ag NPs on the surface result in the high

  14. Application of Power over Ethernet (PoE) in Lighting%以太网供电(PoE)在照明中的应用

    Institute of Scientific and Technical Information of China (English)

    高逸峰; 侯奇锋

    2016-01-01

    After introducing PoE standards including IEEE 802. 3af and IEEE 802. 3at and development of LED lighting technology, this paper discusses an emerging unique technological advantage that PoE application in conventional network equipment shifts to its application in lighting system, and puts forward the problems in subsequent use.%介绍以太网供电标准 IEEE 802.3af、IEEE 802.3at,结合LED照明技术的发展,阐述PoE供电由常规的应用于网络设备过渡到照明系统这一新兴技术独特的技术优势,提出需要在后续使用中注意的相关问题。

  15. Coupled extremely light Ca and Fe isotopes in peridotites

    Science.gov (United States)

    Zhao, Xinmiao; Zhang, Zhaofeng; Huang, Shichun; Liu, Yufei; Li, Xin; Zhang, Hongfu

    2017-07-01

    Large metal stable isotopic variations have been observed in both extraterrestrial and terrestrial samples. For example, Ca exhibits large mass-dependent isotopic variation in terrestrial igneous rocks and mantle minerals (on the order of ∼2‰ variation in 44Ca/40Ca). A thorough assessment and understanding of such isotopic variations in peridotites provides important constraints on the evolution and compositon of the Earth's mantle. In order to better understand the Ca and Fe isotopic variations in terrestrial silicate rocks, we report Ca isotopic compositions in a set of peridotitic xenoliths from North China Craton (NCC), which have been studied for Fe isotopes. These NCC peridotites have large Ca and Fe isotopic variations, with δ44/40Ca ranging from -0.08 to 0.92 (delta value relative to SRM915a) and δ57/54Fe (delta value relative to IRMM-014) ranging from -0.61 to 0.16, and these isotopic variations are correlated with large Mg# (100 × Mg/(Mg + Fe) molar ratio) variation, ranging from 80 to 90. Importantly, NCC Fe-rich peridotites have the lowest 44Ca/40Ca and 57Fe/54Fe ratios in all terrestrial silicate rocks. In contrast, although ureilites, mantle rocks from a now broken differentiated asteroid(s), have large Mg# variation, from 70 to 92, they have very limited δ57Fe/54Fe variation (0.03-0.21, delta value relative to IRMM-014). Our model calculations show that the coupled extremely light Ca-Fe isotopic signatures in NCC Fe-rich peridotites most likely reflect kinetic isotopic fractionation during melt-peridotite reaction on a timescale of several to 104 years. In addition, our new data and compiled literature data show a possible compositional effect on the inter-mineral Ca isotopic fractionation between co-existing clinopyroxene and orthopyroxene pairs.

  16. Visible light induced H2PO(4)(-) removal over CuAlO2 catalyst.

    Science.gov (United States)

    Benreguia, N; Omeiri, S; Bellal, B; Trari, M

    2011-09-15

    The delafossite CuAlO(2) is successfully used for the visible light driven H(2)PO(4)(-) reduction. It is prepared from the nitrates decomposition in order to increase the ratio of reaction surface per given mass. CuAlO(2) is a narrow band gap semiconductor which exhibits a good chemical stability with a corrosion rate of 1.70 μmol year(-1) at neutral pH. The flat band potential (+0.25 V(SCE)) is determined from the Mott-Schottky characteristic. Hence, the conduction band, positioned at (-1.19 V(SCE)), lies below the H(2)PO(4)(-) level yielding a spontaneous reduction under visible illumination. The photocatalytic process is investigated under mild conditions and 30% conversion occurs in less than ~6h with a quantum efficiency of 0.04% under full light. The concentration decreases by a factor of 39% after a second cycle. The photoactivity follows a first order kinetic with a rate constant of 6.6 × 10(-2)h(-1). The possibility of identifying the reaction products via the intensity-potential characteristics is explored. The decrease of the conversion rate over illumination time is due to the competitive water reduction.

  17. Physico-chemical investigation of AlPO/sub 4/ used for production of antacids. Pt. 7. Studies on influence of thermic processing of AlPO/sub 4/ gels on their isotope exchange with /sup 32/PO/sub 4//sup 3 -/

    Energy Technology Data Exchange (ETDEWEB)

    Bem, H. (Politechnika Lodzka (Poland). Katedra Chemii Radiacyjnej); Umbreit, M.H. (Akademia Medyczna, Poznan (Poland))

    1980-01-01

    ''Dry'' AlPO/sub 4/ gels were obtained. After maturation for two weeks, the gels were desalted and dried at room temperature and then successively at 40/sup 0/C and 105/sup 0/C. In parallel, the gels dried only at room temperature were sealed in glass ampoules and heated for 48 hrs at 50/sup 0/C, 60/sup 0/C, 70/sup 0/C or 80/sup 0/C. Isotope exchange was studied. Radioactivity of the gel samples was measured. The specific surface area of AlPO/sub 4/ gels was determined. The gels dried at higher temperatures were found to have larger specific surface areas, but their isotope exchange ability was lower. The obtained results have demonstrated that the specific surface area is not a satisfactory criterion of the medicinal value of AlPO/sub 4/ gels. Structure of surface layers of the sediment must be also considered, which can be determined by isotope exchange in the heterogeneous system, according to the equation: NaH/sub 2//sup 32/PO/sub 4/+AlPO/sub 4/ reversible NaH/sub 2/PO/sub 4/+Al/sup 32/PO/sub 4/.

  18. Characteristics of carbon and hydrogen isotopic compositions of light hydrocarbons

    Institute of Scientific and Technical Information of China (English)

    沈平

    1995-01-01

    Light hydrocarbons named in the present paper refer to the natural gas-associated light oil and condensate 46 light oil and condensate samples from 11 oil-bearing basins of China were collected and their carbon and hydrogen isotopic compositions were analysed in terms of their total hydrocarbons, saturated hydrocarbons and a part of aromatic fractions, and gas-source materials and their sedimentary environments were discussed based on the above-mentioned data and the geological background of each area. From the view of carbon and hydrogen isotopic composition of total hydrocarbons and saturated hydrocarbons, it is revealed that the condensate related to coal-bearing strata is enriched in 13C and D while that related to the source material of type I-II is enriched in 12C. In general, the isotopic composition of carbon is mainly attributed to the inheriting effect of their source materials, whereas that of hydrogen principally reflects the correlationship between hydrogen isotopes and the sedimentary envi

  19. Hydroxyapatite supported Ag{sub 3}PO{sub 4} nanoparticles with higher visible light photocatalytic activity

    Energy Technology Data Exchange (ETDEWEB)

    Hong Xiaoting, E-mail: hanren.xiaoting@gmail.com [School of Chemistry and Environment, South China Normal University, Guangzhou 510006 (China); Wu Xiaohui; Zhang Qiuyun; Xiao Mingfeng; Yang Gelin; Qiu Meirong; Han Guocheng [School of Chemistry and Environment, South China Normal University, Guangzhou 510006 (China)

    2012-03-01

    Hydroxyapatite supported Ag{sub 3}PO{sub 4} nanocomposites have been synthesized by a wet impregnation process. UV-vis absorption spectra show a red shift of the absorption edges for the composite systems compared to pure hydroxyapatite support. The surface structure and morphology of the nanocomposites were characterized by Brunauer-Emmett-Teller (BET) apparatus, X-ray diffraction (XRD), transmission electron microscopy (TEM). The results suggest that Ag{sub 3}PO{sub 4} nanoparticles (6-17 nm in diameter) are well dispersed on the hydroxyapatite support and Ag{sub 3}PO{sub 4} nanoparticles density is larger for the higher Ag{sup +} loading sample. The as-prepared nanocomposite photocatalysts showed a pronounced photocatalytic activity upon decomposition of methylene blue dye in aqueous solution under both visible light (wavelength > 400 nm) and UV-vis light irradiation. A synergic mechanism of inherent photocatalytic capability of Ag{sub 3}PO{sub 4} and the accelerated electron/hole separation resulting from the photoinduced electrons captured by the slow-released Ag{sup +} at the interface of Ag{sub 3}PO{sub 4} and hydroxyapatite is proposed for the nanocomposites on the enhancement of photocatalytic performance in comparison to that of pure Ag{sub 3}PO{sub 4} nanoparticles. The support of hydroxyapatite may also act as an absorbent which favors the mass transfer in heterogeneous photocatalysis reaction.

  20. Synthesis and photoluminescence properties of LiSrPO4:Eu2+ phosphor for solid state lighting

    Science.gov (United States)

    Game, D. N.; Taide, S. T.; Khan, Z. S.; Ingale, N. B.; Omanwar, S. K.

    2016-05-01

    A novel method to prepare orthophosphate LiSrPO4: Eu2+ phosphor for white light-emitting diodes (w-LEDs) is given in this paper. Phosphor was successfully synthesized by Pechini (citrate gel) method which is efficient than conventional high temperature solid state reaction. X-ray powder diffraction (XRD) analysis confirmed the single phase formation of LiSrPO4:Eu2+ with monoclinic crystal structure. Luminescence results showed that the phosphor could be efficiently excited by near UV and exhibited bright blue emission at λem = 420 nm corresponding to 5d- 4f transition of Eu2+. The phosphor exhibits blue emission bands under 350 nm excitation. This mercury-free excitation is useful for solid state lighting and light-emitting diode (LED). Hence it could be useful for solid state lighting and light-emitting diode (LED) application.

  1. Preparation and Characterization of Highly Efficient and Stable Visible-Light-Responsive Photocatalyst AgBr/Ag3PO4

    Directory of Open Access Journals (Sweden)

    Zhang Jinfeng

    2013-01-01

    Full Text Available AgBr/Ag3PO4 photocatalyst was synthesized using a facile coprecipitation method. The photocatalyst was characterized by X-ray powder diffraction (XRD, UV-Vis diffuse reflectance spectroscopy (DRS, scanning electron microscopy (SEM, Brunauer-Emmett-Teller (BET surface areas, and photoluminescence (PL technique. The activity of the photocatalyst was evaluated by the degradation of methyl orange (MO and rhodamine B (RhB. The results showed that the prepared AgBr/Ag3PO4 exhibited excellent performance and much higher photocatalytic activity than the single one under visible-light irradiation. The optimum mole ratio of Br/P in AgBr/Ag3PO4 samples is 0.3. The prepared AgBr/Ag3PO4 photocatalyst was transformed to Ag/AgBr/Ag3PO4 system with excellent property and good stability in the photocatalytic process. The possible mechanisms of the enhanced photocatalytic activity for the AgBr/Ag3PO4 were also discussed in detail.

  2. Application of 210Po isotope dating for chronological assessment of organochlorine pesticides in estuarine sediment

    Directory of Open Access Journals (Sweden)

    G.G. Pandit

    2014-04-01

    The total HCH concentration in the surface sediment samples was in the range of 5.6–13.3 ng/g while total DDT concentration in the surface sediment samples was in the range of 3.2–5.5 ng/g. DDT and γ-HCH were the dominant OCPs in sediments from the creek. The sedimentation rate was determined using 210Po activity measurement in different cores of the sediment and was found to be 0.67 cm/y on average. It was observed that the sediments were highly contaminated during the period of 1970–80 just after the green revolution in India. Total DDT was highest in the 1974–1978 layers of the sediments. Total HCH was highest in the 1972–1976 layers at all the locations.

  3. Light element controlled iron isotope fractionation in planetary cores

    Science.gov (United States)

    Shahar, A.; Hillgren, V. J.; Horan, M. F.; Duke, L.; Mock, T. D.

    2013-12-01

    Using iron isotope fractionations measured in planetary and meteorite samples to trace planetary differentiation or formation has yielded contradictory results. Iron from high-Ti lunar basalts is more enriched in 57Fe/54Fe than mantle-derived terrestrial samples, in contrast to the isotopic similarity for almost every other element between the Earth and Moon. SNC (Shergottite, Nakhlite, Chassigny) and HED (Howardite, Eucrite, Diogenite) meteorites, which are thought to be derived from the mantles of Mars and Vesta, respectively, show no isotopic fractionation relative to chondrites. While the Bulk Silicate Earth (BSE) value is debated, recent work has shown effectively that basalts (mid-ocean ridge basalts, terrestrial basalts, and ocean island basalts) are enriched in 57Fe/54Fe relative to chondrites, but the causes of that fractionation are unclear (Craddock et al. 2013). Angrites, basaltic achondrite meteorites, also show enrichment in δ57Fe (Wang et al. 2012). Possible mechanisms include high-pressure core formation, oxidation during perovskite disproportionation, evaporation during the giant impact, and mantle melting. It is important to reconcile why the Earth's basalts are enriched in 57Fe/54Fe but the meteorites from Mars and Vesta are not. One possible explanation is that Mars and Vesta are smaller and the lower pressure attenuated the potential Fe fractionation during core formation. A second possibility is that the intrinsic oxidation states of the planets are causing the differences. However, another option is that the light elements (e.g. S, C, O, H, Si) in the cores of differentiated bodies control the iron isotope fractionation during differentiation. We have conducted experiments at 1 GPa and 1650-1800°C in a piston cylinder apparatus to address how sulfur, carbon and silicon alloyed with iron affect the iron isotopic fractionation between metallic alloy and silicate melt. We find that sulfur has the greatest effect on the iron isotopic

  4. Isotope effects in photo dissociation of ozone with visible light

    Science.gov (United States)

    Früchtl, Marion; Janssen, Christof; Röckmann, Thomas

    2014-05-01

    Ozone (O3) plays a key role for many chemical oxidation processes in the Earth's atmosphere. In these chemical reactions, ozone can transfer oxygen to other trace gases. This is particularly interesting, since O3 has a very peculiar isotope composition. Following the mass dependent fractionation equation δ17O = 0.52 * δ18O, most fractionation processes depend directly on mass. However, O3 shows an offset to the mass dependent fractionation line. Processes, which show such anomalies, are termed mass independent fractionations (MIF). A very well studied example for a chemical reaction that leads to mass independent fractionation is the O3 formation reaction. To what degree O3 destruction reactions need to be considered in order to understand the isotope composition of atmospheric O3 is still not fully understood and an open question within scientific community. We set up new experiments to investigate the isotope effect resulting from photo dissociation of O3 in the Chappuis band (R1). Initial O3 is produced by an electric discharge. After photolysis O3 is collected in a cold trap at the triple point temperature of nitrogen (63K). O3 is then converted to O2 in order to measure the oxygen isotopes of O3 using isotope ratio mass spectrometry. To isolate O3 photo dissociation (R1) from O3 decomposition (R2) and secondary O3 formation (R3), we use varying amounts of carbon monoxide (CO) as O atom quencher (R4). In this way we suppress the O + O3 reaction (R3) and determine the isotope fractionation in R1 and R2 separately. We present first results on the isotope effects in O3 photo dissociation with visible light in the presence of different bath gases. Results are interpreted based on chemical kinetics modeling. (R1) O3 + hυ → O (3P) + O2 (R2) O3 + O (3P) → 2 O2 (R3) O + O2 + M → O3 + M (R4) O (3P) + CO + M → CO2 + M

  5. Enhanced visible-light photocatalytic performances of Ag3PO4 surface-modified with small amounts of TiO2 and Ag

    Science.gov (United States)

    Wang, Desong; Li, Lei; Luo, Qingzhi; An, Jing; Li, Xueyan; Yin, Rong; Zhao, Mangmang

    2014-12-01

    A novel approach has been developed to prepare an efficient visible-light photocatalyst using Ag3PO4 and TiO2 sol as precursors. First, Ag3PO4 particles were dipped into TiO2 sol for 5 min and were filtered quickly. Second, Ag3PO4 particles adsorbing a small amount of TiO2 sol were aged for 24 h to form TiO2 gel on their surface. Finally, Ag3PO4 particles covered by TiO2 gel were calcined at 450 °C for 2 h to obtain the surface-modified Ag3PO4 sample. The surface-modified Ag3PO4 was characterized by X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, UV-vis diffuse reflection spectroscopy, X-ray photoelectron spectroscopy, and electrochemical impedance spectroscopy. The visible-light photocatalytic performances of the surface-modified Ag3PO4 were evaluated by the photodegradation of methyl orange or phenol solution. The results showed that the surface-modified Ag3PO4 exhibited much higher visible-light photocatalytic activity and stability than pure Ag3PO4. As the amount of TiO2 gel on the Ag3PO4 surface increased, the visible-light photocatalytic activity increased first and then decreased. The surface-modification of Ag3PO4 obviously decreased its solubility in water environment due to the protection of TiO2 and Ag nanocrystals on the surface. The visible-light photocatalytic mechanism of the surface-modified Ag3PO4 has been discussed.

  6. Effect of Phosphate Salts (Na3PO4, Na2HPO4, and NaH2PO4) on Ag3PO4 Morphology for Photocatalytic Dye Degradation under Visible Light and Toxicity of the Degraded Dye Products

    NARCIS (Netherlands)

    Amornpitoksuk, P; Intarasuwan, K; Suwanboon, S; Baltrusaitis, J.

    2013-01-01

    Ag3PO4 was synthesized by the precipitation method using three different types of phosphate salts (Na3PO4, Na2HPO4, and NaH2PO4) as a precipitating agent. Hydrolysis of each phosphate salt gave a specific pH that affected the purity and morphology of the prepared Ag3PO4. The Ag3PO4 prepared from Na2

  7. In-beam gamma-ray spectroscopy of sup 1 sup 9 sup 0 Po: First observation of a low-lying prolate band in Po isotopes

    CERN Document Server

    Van De Vel, K; Andreyev, A N; Page, R D; Kettunen, H; Greenlees, P T; Jones, P; Julin, R; Juutinen, S; Kankaanpaeae, H; Keenan, A; Kuusiniemi, P; Leino, M; Muikku, M; Nieminen, P; Rahkila, P; Uusitalo, J; Eskola, Kari J; Hürstel, A; Le Coz, Y L; Smith, M B; Van Duppen, P; Wyss, R

    2003-01-01

    Gamma rays from excited states of sup 1 sup 9 sup 0 Po have been observed using the Jurosphere Ge-detector array coupled to the RITU gas-filled separator. They were associated with a collective band which from spin 4 Planck constant onwards resembles the prolate rotational bands known in the isotones sup 1 sup 8 sup 8 Pb and sup 1 sup 8 sup 6 Hg. This indicates that in sup 1 sup 9 sup 0 Po the prolate configuration becomes yrast above I=2 Planck constant. The experimental results are interpreted in a two-band mixing calculation and are in agreement with alpha-decay data and potential energy surface calculations. (orig.)

  8. Tunable and white light emitting AlPO4 mesoporous glass by design of inorganic/organic luminescent species

    Directory of Open Access Journals (Sweden)

    Jin He

    2015-04-01

    Full Text Available The realization of tunable and white light emitting sources employed by UV-LED with single-host phosphors has been an exciting development in the search for high luminous efficiency and excellent color rendering index white-light source. A tunable and white light emitting mesoporous glass was prepared by utilizing both inorganic/organic (Europium/coumarin luminescent species in the meso-structure. The tunable and white light emission was deliberately designed by CIE calculation based on the individual emission spectra, which was realized by tailoring the emission of Eu2+/Eu3+ ions and coumarin 535 in sol-gel AlPO4 mesoporous glass. This simple and versatile procedure is not limited in the combination of rare earth and organic dye and is therefore extendable to other luminescent species in meso-structure for color-tunable efficient solid-state lighting sources.

  9. Tunable and white light emitting AlPO{sub 4} mesoporous glass by design of inorganic/organic luminescent species

    Energy Technology Data Exchange (ETDEWEB)

    He, Jin; Li, Rihong, E-mail: lirihong@siom.ac.cn; Yuan, Xinqiang; Zhang, Long, E-mail: lzhang@siom.ac.cn [Key Laboratory of Materials for High Power Lasers, Shanghai Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, Shanghai 201800 (China); Wang, Yan [Key Laboratory of Materials for High Power Lasers, Shanghai Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, Shanghai 201800 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Xu, Shiqing [College of Materials Science and Engineering, China Jiliang University, Hangzhou, Zhejiang 310018 (China)

    2015-04-01

    The realization of tunable and white light emitting sources employed by UV-LED with single-host phosphors has been an exciting development in the search for high luminous efficiency and excellent color rendering index white-light source. A tunable and white light emitting mesoporous glass was prepared by utilizing both inorganic/organic (Europium/coumarin) luminescent species in the meso-structure. The tunable and white light emission was deliberately designed by CIE calculation based on the individual emission spectra, which was realized by tailoring the emission of Eu{sup 2+}/Eu{sup 3+} ions and coumarin 535 in sol-gel AlPO{sub 4} mesoporous glass. This simple and versatile procedure is not limited in the combination of rare earth and organic dye and is therefore extendable to other luminescent species in meso-structure for color-tunable efficient solid-state lighting sources.

  10. Nuclear structure of light Ca and heavy Cr isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Buerger, A.

    2007-07-01

    In the present thesis, the shell structure in exotic nuclei has been investigated. The focus of the work was on finding new experimental data in neutron-rich Cr and proton-rich Ca isotopes. The investigation of light Ca isotopes concentrated on the nucleus {sup 36}Ca which was produced in a knockout reaction from a radioactive {sup 37}Ca beam. For {sup 36}Ca, the excitation energy of the first 2{sup +} state has been measured for the first time. Furthermore, momentum distributions were analyzed using a Monte-Carlo simulation of the knockout reaction. This analysis yielded the contributions of neutrons from individual orbitals to the total knockout cross section. In principle, these may be used to calculate spectroscopic factors, but such a calculation is hampered by difficulties of present knockout-reaction models in predicting precise single-particle cross sections. The measured branching ratio to the ground and excited states, on the other hand, is close to the predicted value. A remaining difference might be due to emission of protons which cannot be detected with the present experimental setup. Both the branching ratio and the large excitation energy are compatible with a large N=16 gap in {sup 36}Ca that leads to relatively pure configurations both in the ground state and the excited 2{sup +} state. As a by-product of the experiment, two excitation energies in the T=2 nuclei {sup 32}Ar and {sup 28}S have been confirmed, and two {gamma}-ray transitions have been observed for the first time in {sup 37}Ca. While the mirror energy differences in the T=2 pairs {sup 36}Ca-{sup 36}S, {sup 32}Ar-{sup 32}Si, and {sup 28}S-{sup 28}Mg can be reproduced in shell model calculations using a modified USD interaction, these modifications are not sufficient to explain the mirror energy differences for the pair {sup 37}Ca-{sup 37}Cl. In the heavy Cr isotopes, new experimental evidence for a sub-shell closure at N=32 was found in a measurement of B(E2) values using high

  11. Nanocomposite of exfoliated bentonite/g-C3N4/Ag3PO4 for enhanced visible-light photocatalytic decomposition of Rhodamine B.

    Science.gov (United States)

    Ma, Jianfeng; Huang, Daiqin; Zhang, Wenyi; Zou, Jing; Kong, Yong; Zhu, Jianxi; Komarneni, Sridhar

    2016-11-01

    Novel visible-light-driven heterojunction photocatalyst comprising exfoliated bentonite, g-C3N4 and Ag3PO4 (EB/g-C3N4/Ag3PO4) was synthesized by a facile and green method. The composites EB/g-C3N4/Ag3PO4 were characterized by X-ray diffraction, Transmission electron microscopy, Fourier transform infrared spectroscopy, UV-Vis diffuse reflectance spectroscopy and the Brunauer, Emmett, and Teller (BET) surface area method. Under visible light irradiation, EB/g-C3N4/Ag3PO4 composites displayed much higher photocatalytic activity than that of either pure g-C3N4 or pure Ag3PO4 in the degradation of Rhodamine B (RhB). Among the hybrid photocatalysts, EB/g-C3N4/Ag3PO4 composite containing 20 wt% Ag3PO4 exhibited the highest photocatalytic activity for the decolorization of RhB. Under the visible-light irradiation, the RhB dye was completely decolorized in less than 60 min. The enhanced photocatalytic performance is attributed to the stable structure, enlarged surface area, strong adsorbability, strong light absorption ability, and high-efficiency separation rate of photoinduced electron-hole pairs. Our finding paves a way to design highly efficient and stable visible-light-induced photocatalysts for practical applications in wastewater treatment.

  12. Probing new light force-mediators by isotope shift spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Berengut, Julian C. [New South Wales Univ., Sydney, NSW (Australia). School of Physics; Budker, Dmitry [Mainz Univ. (Germany). Helmholtz-Inst. Mainz; California Univ., Berkeley, CA (United States). Physics Dept.; Lawrence Berkeley National Laboratory, Berkeley, CA (United States). Nuclear Science Div.; Delaunay, Cedric [Savoie Mont Blanc Univ., Annecy-le-Vieux (France). Laboratoire d' Annecy-le-Vieux de Physique Theorique LAPTh; and others

    2017-04-15

    In this Letter we explore the potential of probing new light force-carriers, with spin-independent couplings to the electron and the neutron, using precision isotope shift spectroscopy. We develop a formalism to interpret linear King plots as bounds on new physics with minimal theory inputs. We focus only on bounding the new physics contributions that can be calculated independently of the Standard Model nuclear effects. We apply our method to existing Ca{sup +} data and project its sensitivity to possibly existing new bosons using narrow transitions in other atoms and ions (specifically, Sr and Yb). Future measurements are expected to improve the relative precision by five orders of magnitude, and can potentially lead to an unprecedented sensitivity for bosons within the 10 keV to 10 MeV mass range.

  13. Synthesis and luminescence properties of Ca5(PO43Cl:Eu2+ phosphor for solid state lighting

    Directory of Open Access Journals (Sweden)

    Deorao N. Game

    2016-03-01

    Full Text Available A novel method to prepare Eu2+ doped chlorapatite phosphor Ca5(PO43Cl useful for solid state lighting has been given in this paper. The phosphor was synthesized by the Pechini (citrate gel method which turned out to be more efficient than the conventional high temperature solid state reaction. The results of the photoluminescence (PL investigation revealed that it was possible to efficiently excite the phosphor by a UV–visible light from 220 to 430nm; the phosphor exhibited a bright blue emission at the wavelength λem=456nm for the excitation wavelength λex=350nm of near-ultraviolet light. The developed phosphor emits in blue and, hence, could provide one of the three (RGB primary color components in a phosphor-converted LED-producing white light.

  14. Rare-earth free yellow-green emitting NaZnPO4:Mn phosphor for lighting applications

    Science.gov (United States)

    Haranath, D.; Mishra, S.; Yadav, S.; Sharma, R. K.; Kandpal, L. M.; Vijayan, N.; Dalai, M. K.; Sehgal, G.; Shanker, V.

    2012-11-01

    Manganese-doped sodium zinc phosphate (NaZnPO4:Mn) phosphor with exceptional features having ultra-violet (UV) to visible absorption (300-470 nm), yellow-green (˜543 nm) broad-band photoluminescence (PL), and appreciable color co-ordinates (x = 0.39, y = 0.58) is reported. It has a crystal structure consisting of discrete PO4 tetrahedra linked by ZnO4 and NaO4 distorted tetrahedral such that three tetrahedra, one of each kind, share one corner. The presence of UV sensitive Zn-O-Zn bonds and their efficient energy transfer to Mn2+ ions resulted in brightest PL and external quantum yield of 63% at 418 nm. Our experiment demonstrated the possibility of producing inexpensive white-light emitting devices for future.

  15. Bioaccumulation of polonium (210Po, uranium (234U, 238U isotopes and trace metals in mosses from Sobieszewo Island, northern Poland

    Directory of Open Access Journals (Sweden)

    Boryło A.

    2013-04-01

    Full Text Available The objective of this study was determination of the polonium (210Po, uranium (234U and 238U radionuclides and trace metals (Pb, Fe, Zn, Cu, Ni, Cd, Hg concentrations in mosses samples from Sobieszewo Island near the phosphogypsum waste dump in Wiślinka (northern Poland. The obtained results revealed that the concentrations of 210Po, 234U, and 238U in the two analyzed kinds of mosses: Pleurozium schreberi and Dicranum scoparium were similar. Among the analyzed trace metals the highest concentration in mosses was recorded for iron, while the lowest for nickel, cadmium and mercury. The obtained studies showed that the sources of polonium and uranium isotopes, as well as trace metals in analyzed mosses are air city contaminations transported from Gdańsk and from existing in the vicinity the phosphogypsum waste heap in Wiślinka (near Gdańsk.

  16. Final Report on Isotope Ratio Techniques for Light Water Reactors

    Energy Technology Data Exchange (ETDEWEB)

    Gerlach, David C.; Gesh, Christopher J.; Hurley, David E.; Mitchell, Mark R.; Meriwether, George H.; Reid, Bruce D.

    2009-07-01

    The Isotope Ratio Method (IRM) is a technique for estimating the energy or plutonium production in a fission reactor by measuring isotope ratios in non-fuel reactor components. The isotope ratios in these components can then be directly related to the cumulative energy production with standard reactor modeling methods.

  17. Ag3PO4/graphene-oxide composite with remarkably enhanced visible-light-driven photocatalytic activity toward dyes in water.

    Science.gov (United States)

    Chen, Guodong; Sun, Meng; Wei, Qin; Zhang, Yongfang; Zhu, Baocun; Du, Bin

    2013-01-15

    Ag(3)PO(4)/graphene-oxide (Ag(3)PO(4)/GO) composite has been synthesized by a liquid phase deposition method, and used for the photodegradation of organic dyes in water under visible light. The as-synthesized samples were characterized by X-ray diffraction, scanning electron microscope, N(2) sorption-desorption, and UV-vis diffuse reflectance spectra. The SEM image indicated that Ag(3)PO(4) particles were mainly distributed on the surface of GO sheets uniformly. DRS analysis revealed that the samples had good visible light response. The photocatalytic activity of Ag(3)PO(4)/GO composite was evaluated by decomposing of dyes (such as methyl orange, rhodamine B) in water under visible or UV-vis light irradiation. The degradation results indicated that the photocatalytic performance of Ag(3)PO(4)/GO was greatly enhanced due to the improved adsorption performance and separation efficiency of photo-generated carriers. The Ag(3)PO(4)/GO composite with GO content of 15 wt.% exhibited superior activity under visible light irradiation. After 50 min of reaction, the degradation ratio of MO was about 86.7%, while RhB solution could be completely degraded within 30 min of reaction. Further study proved that the direct oxidation of pollutants by holes has played a major role in the degradation process. The results of this work would provide a new sight for the construction of visible light-responsive photocatalysts with high performance.

  18. 可见光驱动 Ag3PO4催化剂的可控制备及活性评价%Controlled synthesis and activity evaluation of visible-light-driven Ag3PO4 catalyst

    Institute of Scientific and Technical Information of China (English)

    葛明; 崔海涛; 刘美玲

    2014-01-01

    Three Ag3 PO4 photocatalysts were controlled synthesized via a facile precipitation method using AgNO3 and Na3 PO4 ,Na2 HPO4 ,NaH2 PO4 as raw materials. The samples were characterized by XRD,FE-SEM,UV-Vis,FTIR and BET. The photocatalytic activities of three Ag3 PO4 samples were evaluated for RhB degradation using visible light. Using Na3 PO4 ,Na2 HPO4 and NaH2 PO4 to prepared Ag3 PO4 ,the de-gree of crystallinity of sample was gradually increased,and the particle size was increased,the reaction rate constant for RhB degradation over the as-obtained Ag3 PO4 sample was 0. 03,0. 10,0. 15 min - 1 ,re-spectively. Na2 HPO4 As raw materials,the as-obtained Ag3 PO4 photocatalyst with higher yield exhibited the excellent photocatalytic activity. Under natural sunlight irradiation,the Ag3 PO4 photocatalyst could be reused. The photocatalytic activity of the photocatalyst decreased when Ag0 were produced during the pho-tocatalytic process.%以 AgNO3和 Na3 PO4、Na2 HPO4、NaH2 PO4为原料,采用简易液相沉淀法可控制备3种 Ag3 PO4光催化剂,采用 XRD、FE-SEM、UV-Vis、FTIR 及 BET 表征。以罗丹明 B 为目标污染物,评价样品的可见光催化活性。结果表明,采用 Na3 PO4、Na2 HPO4、NaH2 PO4制备 Ag3 PO4,样品的结晶度逐渐增加,粒径逐渐增大,3种样品均能吸收可见光,去除水体中罗丹明 B 的反应速率常数分别为0.03,0.10,0.15 min -1。以 Na2 HPO4为原料可获取高产率、高活性Ag3 PO4光催化剂。真实太阳光照射下,Ag3 PO4光催化剂可重复利用。单质银的产生降低了催化剂的光催化活性。

  19. Segregation of isotopes of heavy metals due to light-induced drift: results and problems

    CERN Document Server

    Sapar, A; Poolamäe, R; Sapar, L

    2007-01-01

    Atutov and Shalagin (1988) proposed light-induced drift (LID) as a physically well understandable mechanism to explain the formation of isotopic anomalies observed in CP stars. We generalized the theory of LID and applied it to diffusion of heavy elements and their isotopes in quiescent atmospheres of CP stars. Diffusional segregation of isotopes of chemical elements is described by the equations of continuity and diffusion velocity. Computations of the evolutionary sequences for abundances of mercury isotopes in several model atmospheres have been made using the Fortran 90 program SMART, composed by the authors. Results confirm predominant role of LID in separation of isotopes.

  20. Enhancing visible light photocatalytic activity of direct Z-scheme SnS{sub 2}/Ag{sub 3}PO{sub 4} heterojunction photocatalysts

    Energy Technology Data Exchange (ETDEWEB)

    Luo, Jin, E-mail: lj328520504@126.com; Zhou, Xiaosong; Ma, Lin; Xu, Limei; Xu, Xuyao; Du, Zhihua; Zhang, Jinquan

    2016-09-15

    Highlights: • Novel direct Z-scheme SnS{sub 2}/Ag{sub 3}PO{sub 4} heterojunction photocatalysts are synthesized. • SnS{sub 2}/Ag{sub 3}PO{sub 4} exhibits much higher photocatalytic activity than pure SnS{sub 2} and Ag{sub 3}PO{sub 4}. • A possible photocatalytic mechanism was discussed in detail. - Abstract: Novel direct Z-scheme SnS{sub 2}/Ag{sub 3}PO{sub 4} heterojunction photocatalysts were successfully fabricated with SnS{sub 2} nanoplates hybridized by Ag{sub 3}PO{sub 4} nanoparticals via a facile hydrothermal and precipitation method and applied for the photocatalytic degradation of methyl orange in aqueous solution under visible light irradiation (λ > 420 nm). It was found that the photocatalytic performance of the SnS{sub 2} (2.0 wt%)/Ag{sub 3}PO{sub 4} heterojunction photocatalyst with 2.0 wt% SnS{sub 2} content was much higher than that of individual SnS{sub 2} and Ag{sub 3}PO{sub 4}. The enhanced photocatalytic activity could be ascribed to the efficient separation of photogenerated electrons and holes through the formation of direct Z-scheme system composed of SnS{sub 2} and Ag{sub 3}PO{sub 4}. Furthermore, the recycling experiments revealed that the photocorrosion behavior of Ag{sub 3}PO{sub 4} was strongly inhibited by SnS{sub 2}, it may be due to the photogenerated electrons of Ag{sub 3}PO{sub 4} would be quickly combined with the photogenerated holes of SnS{sub 2}. This work will be useful for the design of other direct Z-scheme visible-light-driven photocatalytic systems for application in energy conversion and environmental remediation.

  1. A novel visible light-driven Ag3PO4/SBA-15 nanocomposite: Preparation and application in the photo-degradation of pollutants

    Science.gov (United States)

    Chai, Yuanyuan; Wang, Li; Ren, Jia; Dai, Wei-Lin

    2015-01-01

    A novel visible light-driven environmental-benign Ag3PO4/SBA-15 nanocomposite photo-catalyst was synthesized for the photo-degradation of pollutants. The exploration on adsorption and photo-catalysis of dye or organic pollution for the nanocomposite was carried out. The adsorption capability for Ag3PO4/SBA-15 nanocomposite increases by 3 times compared with that of the Ag3PO4 particles. The photo-catalytic activity of nanocomposite is higher than pristine Ag3PO4 nanoparticle for the degradation of RhB or MO under visible light irradiation (λ > 420 nm). The effect of Ag3PO4 loading on the catalytic performance was also studied. The results show that the optimum degradation is achieved over 20% Ag3PO4/SBA-15. Compared to pure Ag3PO4 nanoparticle, the most efficient catalyst showed 8 times higher photo-catalytic activity for the degradation of RhB. The Ag3PO4/SBA-15 catalysts were systematically characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), UV-Vis diffuse reflectance spectroscopy (DRS), and N2-adsorption-desorption isotherms (BET). A possible mechanism scheme regarding photo-degradation enhancement induced by dye enrichments has been proposed on the Ag3PO4/SBA-15 nanocomposite. Additionally, the SBA-15 support can enhance the efficiency of separation of catalyst from the reaction mixture, implying that the Ag3PO4 loading on the SBA-15 catalyst will not result in the extra environment and health problems and reduce the cost of wastewater treatment.

  2. A chemical bath deposition route to facet-controlled Ag{sub 3}PO{sub 4} thin films with improved visible light photocatalytic activity

    Energy Technology Data Exchange (ETDEWEB)

    Gunjakar, Jayavant L.; Jo, Yun Kyung; Kim, In Young; Lee, Jang Mee; Patil, Sharad B. [Department of Chemistry and Nanoscience, College of Natural Sciences, Ewha Womans University, Seoul 03760 (Korea, Republic of); Pyun, Jae-Chul [Department of Materials Science and Engineering, College of Engineering, Yonsei University, Seoul (Korea, Republic of); Hwang, Seong-Ju, E-mail: hwangsju@ewha.ac.kr [Department of Chemistry and Nanoscience, College of Natural Sciences, Ewha Womans University, Seoul 03760 (Korea, Republic of)

    2016-08-15

    A facile, economic, and reproducible chemical bath deposition (CBD) method is developed for the fabrication of facet-controlled Ag{sub 3}PO{sub 4} thin films with enhanced visible light photocatalytic activity. The fine-control of bath temperature, precursor, complexing agent, substrate, and solution pH is fairly crucial in preparing the facet-selective thin film of Ag{sub 3}PO{sub 4} nanocrystal. The change of precursor from silver nitrate to silver acetate makes possible the tailoring of the crystal shape of Ag{sub 3}PO{sub 4} from cube to rhombic dodecahedron and also the bandgap tuning of the deposited films. The control of [Ag{sup +}]/[phosphate] ratio enables to maximize the loading amount of Ag{sub 3}PO{sub 4} crystals per the unit area of the deposited film. All the fabricated Ag{sub 3}PO{sub 4} thin films show high photocatalytic activity for visible light-induced degradation of organic molecules, which can be optimized by tailoring the crystal shape of the deposited crystals. This CBD method is also useful in preparing the facet-controlled hybrid film of Ag{sub 3}PO{sub 4}–ZnO photocatalyst. The present study clearly demonstrates the usefulness of the present CBD method for fabricating facet-controlled thin films of metal oxosalt and its nanohybrid. - Highlights: • The crystal facet of Ag{sub 3}PO{sub 4} films can be tuned by chemical bath deposition. • The crystal shape of Ag{sub 3}PO{sub 4} is tailorable from cube to rhombic dodecahedron. • Facet-tuned Ag{sub 3}PO{sub 4} film shows enhanced visible light photocatalyst activity.

  3. Ag3PO4的可见光光催化性能及机理分析%Ag3PO4∶ Visible Light Photocatalytic Performance and Mechanism

    Institute of Scientific and Technical Information of China (English)

    王韵芳; 樊彩梅

    2012-01-01

    Visible light photocatalytic material Ag3PO4 was prepared by precipitation replacement method and characterized by using XRD, UV-Vis and XPS. The photocatalytic activity was evaluated by means of degradation of micro-organic pollutants in water. The photocatalytic mechanism was discussed based on the active species during photocatlytic process and band structure. The results showed that the band gap was about 1.9 eV, Ag+ on the catalyst surface might capture photoelectron e~ and the lower valence band potential of Ag3PO4 All of these would help for Ag3PO4 to separate e‐-h+ pairs generated under visible light irradiation and the formation of reactive species ·OH. After 60 min visible light irradiation, the degradation rate of methyl orange and humic acid with initial concentration of 15 mg·L-1 reached 97% and 82%, respectively, by using 0.6 g·L-1 Ag3PO4 This result is better than that of TiO2-P25 40% and 25% at the same experimental conditions.%采用沉淀置换法制备了可见光光催化剂Ag3PO4,利用XRD、UV-Vis及XPS等对其进行了结构特性分析,以水中微污染有机物的降解评价了Ag3PO4的光催化活性,并通过活性物种及能带结构的分析对催化剂的光催化机理进行了推测.结果表明,Ag3PO4的带隙能约为1.9 eV、催化剂表面存在的Ag+可捕获光生e-、催化剂的价带电位较低,这有利于Ag3PO4在可见光照射下产生的e--h+的分离及活性物种·OH的形成.经60 min可见光光催化反应,15 mg·L-1的甲基橙和腐殖酸的降解率分别达97%和82%,比同等条件下TiO2-P25的降解率还高40%和25%,光催化剂Ag3PO4的用量为0.6 g·L-1.

  4. Oxygen isotope ratios of PO4: an inorganic indicator of enzymatic activity and P metabolism and a new biomarker in the search for life.

    Science.gov (United States)

    Blake, R E; Alt, J C; Martini, A M

    2001-02-27

    The distinctive relations between biological activity and isotopic effect recorded in biomarkers (e.g., carbon and sulfur isotope ratios) have allowed scientists to suggest that life originated on this planet nearly 3.8 billion years ago. The existence of life on other planets may be similarly identified by geochemical biomarkers, including the oxygen isotope ratio of phosphate (delta(18)O(p)) presented here. At low near-surface temperatures, the exchange of oxygen isotopes between phosphate and water requires enzymatic catalysis. Because enzymes are indicative of cellular activity, the demonstration of enzyme-catalyzed PO(4)-H(2)O exchange is indicative of the presence of life. Results of laboratory experiments are presented that clearly show that delta(18)O(P) values of inorganic phosphate can be used to detect enzymatic activity and microbial metabolism of phosphate. Applications of delta(18)O(p) as a biomarker are presented for two Earth environments relevant to the search for extraterrestrial life: a shallow groundwater reservoir and a marine hydrothermal vent system. With the development of in situ analytical techniques and future planned sample return strategies, delta(18)O(p) may provide an important biosignature of the presence of life in extraterrestrial systems such as that on Mars.

  5. A novel visible light-driven Ag{sub 3}PO{sub 4}/SBA-15 nanocomposite: Preparation and application in the photo-degradation of pollutants

    Energy Technology Data Exchange (ETDEWEB)

    Chai, Yuanyuan; Wang, Li; Ren, Jia; Dai, Wei-Lin, E-mail: wldai@fudan.edu.cn

    2015-01-01

    Graphical abstract: - Highlights: • Highly efficient visible-light-driven Ag{sub 3}PO{sub 4}/SBA-15 nanocomposite. • Application in the photo-degradation of RhB. • Synthesis from a facile and simple colloidal method. • 20%-Ag{sub 3}PO{sub 4}/SBA-15 shows 8 times faster degradation rate than Ag{sub 3}PO{sub 4}. • Super stability and recycling ability. - Abstract: A novel visible light-driven environmental-benign Ag{sub 3}PO{sub 4}/SBA-15 nanocomposite photo-catalyst was synthesized for the photo-degradation of pollutants. The exploration on adsorption and photo-catalysis of dye or organic pollution for the nanocomposite was carried out. The adsorption capability for Ag{sub 3}PO{sub 4}/SBA-15 nanocomposite increases by 3 times compared with that of the Ag{sub 3}PO{sub 4} particles. The photo-catalytic activity of nanocomposite is higher than pristine Ag{sub 3}PO{sub 4} nanoparticle for the degradation of RhB or MO under visible light irradiation (λ > 420 nm). The effect of Ag{sub 3}PO{sub 4} loading on the catalytic performance was also studied. The results show that the optimum degradation is achieved over 20% Ag{sub 3}PO{sub 4}/SBA-15. Compared to pure Ag{sub 3}PO{sub 4} nanoparticle, the most efficient catalyst showed 8 times higher photo-catalytic activity for the degradation of RhB. The Ag{sub 3}PO{sub 4}/SBA-15 catalysts were systematically characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), UV–Vis diffuse reflectance spectroscopy (DRS), and N{sub 2}-adsorption–desorption isotherms (BET). A possible mechanism scheme regarding photo-degradation enhancement induced by dye enrichments has been proposed on the Ag{sub 3}PO{sub 4}/SBA-15 nanocomposite. Additionally, the SBA-15 support can enhance the efficiency of separation of catalyst from the reaction mixture, implying that the Ag{sub 3}PO{sub 4} loading on the SBA-15 catalyst will not result in the extra environment and health

  6. Ag{sub 3}PO{sub 4}/graphene-oxide composite with remarkably enhanced visible-light-driven photocatalytic activity toward dyes in water

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Guodong [Key Laboratory of Chemical Sensing and Analysis in Universities of Shandong, School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022 (China); Sun, Meng, E-mail: smlcu@163.com [School of Resources and Environment, University of Jinan, Jinan 250022 (China); Wei, Qin [Key Laboratory of Chemical Sensing and Analysis in Universities of Shandong, School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022 (China); Zhang, Yongfang; Zhu, Baocun [School of Resources and Environment, University of Jinan, Jinan 250022 (China); Du, Bin, E-mail: binduujn@163.com [School of Resources and Environment, University of Jinan, Jinan 250022 (China); Key Laboratory of Chemical Sensing and Analysis in Universities of Shandong, School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022 (China)

    2013-01-15

    Highlights: ► Ag{sub 3}PO{sub 4}/GO shows enhanced photocatalytic activity in degradation of dyes in water. ► The sample with GO content of 15% exhibits the best activity under visible light. ► The combination of GO enhances the separation efficiency of photo-induced carriers. -- Abstract: Ag{sub 3}PO{sub 4}/graphene-oxide (Ag{sub 3}PO{sub 4}/GO) composite has been synthesized by a liquid phase deposition method, and used for the photodegradation of organic dyes in water under visible light. The as-synthesized samples were characterized by X-ray diffraction, scanning electron microscope, N{sub 2} sorption–desorption, and UV–vis diffuse reflectance spectra. The SEM image indicated that Ag{sub 3}PO{sub 4} particles were mainly distributed on the surface of GO sheets uniformly. DRS analysis revealed that the samples had good visible light response. The photocatalytic activity of Ag{sub 3}PO{sub 4}/GO composite was evaluated by decomposing of dyes (such as methyl orange, rhodamine B) in water under visible or UV–vis light irradiation. The degradation results indicated that the photocatalytic performance of Ag{sub 3}PO{sub 4}/GO was greatly enhanced due to the improved adsorption performance and separation efficiency of photo-generated carriers. The Ag{sub 3}PO{sub 4}/GO composite with GO content of 15 wt.% exhibited superior activity under visible light irradiation. After 50 min of reaction, the degradation ratio of MO was about 86.7%, while RhB solution could be completely degraded within 30 min of reaction. Further study proved that the direct oxidation of pollutants by holes has played a major role in the degradation process. The results of this work would provide a new sight for the construction of visible light-responsive photocatalysts with high performance.

  7. Highly Efficient Quantum Sieving in Porous Graphene-like Carbon Nitride for Light Isotopes Separation

    Science.gov (United States)

    Qu, Yuanyuan; Li, Feng; Zhou, Hongcai; Zhao, Mingwen

    2016-01-01

    Light isotopes separation, such as 3He/4He, H2/D2, H2/T2, etc., is crucial for various advanced technologies including isotope labeling, nuclear weapons, cryogenics and power generation. However, their nearly identical chemical properties made the separation challenging. The low productivity of the present isotopes separation approaches hinders the relevant applications. An efficient membrane with high performance for isotopes separation is quite appealing. Based on first-principles calculations, we theoretically demonstrated that highly efficient light isotopes separation, such as 3He/4He, can be reached in a porous graphene-like carbon nitride material via quantum sieving effect. Under moderate tensile strain, the quantum sieving of the carbon nitride membrane can be effectively tuned in a continuous way, leading to a temperature window with high 3He/4He selectivity and permeance acceptable for efficient isotopes harvest in industrial application. This mechanism also holds for separation of other light isotopes, such as H2/D2, H2/T2. Such tunable quantum sieving opens a promising avenue for light isotopes separation for industrial application. PMID:26813491

  8. Thermally stable white-emitting single composition Na(Sr,Ba)PO4:Eu2+, Mn2+ phosphor for near-ultraviolet-pumped light-emitting diodes.

    Science.gov (United States)

    Choi, Sungho; Yun, Young Jun; Kim, Sue Jin; Jung, Ha-Kyun

    2013-04-15

    Eu(2+) and Mn(2+) codoped, white-emitting Na(Sr,Ba)PO(4) phosphors are prepared, and their emission properties, especially for thermal stability, are thoroughly investigated. The thermal quenching and Eu(2+)/Mn(2+) energy transfer efficiency are totally different in the ratio of alkaline earth metals in host composition, NaBaPO(4), Na(Sr(0.5)Ba(0.5))PO(4), and NaSrPO(4), respectively. Furthermore, by using near-ultraviolet light-emitting diodes (LEDs) and the corresponding Na(Sr(0.5)Ba(0.5))PO(4):Eu(2+), Mn(2+) phosphor as light converters, we demonstrate a bright and thermally stable white-emitting LED. The resultant LED exhibits a warm white light [~4900 K, CIE coordinates of (0.33, 0.31)] with excellent thermal and hydrolytic stabilities comparable to those of commercially available ones, Y(3)Al(5)O(12):Ce(3+) and BaMg(2)Al(16)O(27):Eu(2+). The proposed composition, with its efficient energy transfer, could enable Eu(2+) and Mn(2+) codoped Na(Sr,Ba)PO(4) to be a promising single component phosphor for cost-effective white-emitting LEDs.

  9. Fabrication of novel Ag{sub 3}PO{sub 4}/BiOBr heterojunction with high stability and enhanced visible-light-driven photocatalytic activity

    Energy Technology Data Exchange (ETDEWEB)

    Mehraj, Owais [Department of Chemistry, Aligarh Muslim University, Aligarh 202002 (India); Mir, Niyaz A. [Solid State and Structural Chemistry Unit, Indian Institute of Science, Bangalore 560012 (India); Pirzada, Bilal M. [Department of Chemistry, Aligarh Muslim University, Aligarh 202002 (India); Sabir, Suhail, E-mail: sabirsuhail09@gmail.com [Department of Chemistry, Aligarh Muslim University, Aligarh 202002 (India)

    2015-03-30

    Graphical abstract: - Highlights: • Ag{sub 3}PO{sub 4}/BiOBr hybrids with exceptionally high visible light photocatalytic activity were synthesized through simple co-precipitation method. • The enhanced activity of Ag{sub 3}PO{sub 4}/BiOBr hybrids was attributed to the efficient charge separation and increased surface area. • The as synthesized Ag{sub 3}PO{sub 4}/BiOBr hybrids displayed high stability. • The high stability of Ag{sub 3}PO{sub 4}/BiOBr hybrids was attributed to the fast transfer of electrons from conduction band of Ag{sub 3}PO{sub 4} to the conduction band of BiOBr. - Abstract: Herein, we report a facile and effective method to enhance the photocatalytic activity of bismuth oxybromide (BiOBr) semiconductor through the fabrication of heterojunction with Ag{sub 3}PO{sub 4}. The as synthesized Ag{sub 3}PO{sub 4}/BiOBr microspheres were characterized with transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS), X–ray diffraction (XRD) and UV–vis diffuse reflectance spectroscopy (DRS). The new Ag{sub 3}PO{sub 4}/BiOBr heterojunctions exhibited wide absorption in the visible-light region and compared to pure BiOBr and Ag{sub 3}PO{sub 4} samples displayed exceptionally high photocatalytic activity for the degradation of typical organic pollutants such as Rhodamine B (RhB) and phenol. The optimal Ag/Bi weight ratio in Ag{sub 3}PO{sub 4}/BiOBr microsphere (AB7) was found to be 0.7. The enhanced photocatalytic activity was related to the efficient separation of electron–hole pairs derived from matching band potentials between BiOBr and Ag{sub 3}PO{sub 4} which results into the generation of natural energy bias at heterojunction and subsequent transfer of photoinduced charge carriers. Moreover, the synthesized samples exhibited almost no loss of activity even after 6 recycling runs indicating their high photocatalytic stability. Considering the facile and environment friendly route for the

  10. BiPO{sub 4}/BiOBr p–n junction photocatalysts: One-pot synthesis and dramatic visible light photocatalytic activity

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Zhang Sheng, E-mail: lzsliu2008@hotmail.com [School of Material Science and Engineering, China University of Mining and Technology, Xuzhou 221116 (China); Wu, Bian Tao [School of Information and Electrical Engineering, China University of Mining and Technology, Xuzhou 221116 (China); Niu, Ji Nan; Feng, Pei Zhong; Zhu, Ya Bo [School of Material Science and Engineering, China University of Mining and Technology, Xuzhou 221116 (China)

    2015-03-15

    Highlights: • BiPO{sub 4}/BiOBr p–n junction photocatalysts were synthesized by a solvothermal method. • BiPO{sub 4}/BiOBr composites were constructed by inlaying BiPO{sub 4} particles into BiOBr microspheres. • BiPO{sub 4}/BiOBr photocatalysts exhibited the enhanced photocatalytic activity. • ·O{sub 2}{sup −} and h{sup +} were the main active species responsible for the degradation of RhB. - Abstract: BiPO{sub 4}/BiOBr p–n junction photocatalysts were successfully synthesized via a facile one-pot solvothermal method. The products were characterized by XRD, FE-SEM, HRTEM, XPS, DRS, PL and EIS. The obtained BiPO{sub 4}/BiOBr composites were constructed by inlaying BiPO{sub 4} nanoparticles into BiOBr hierarchical microspheres. Compared with BiPO{sub 4} and BiOBr, they exhibited significantly enhanced visible light photocatalytic activity towards the degradation of Rhodamine B (RhB). Among them, 10% BiPO{sub 4}/BiOBr showed the maximum value of the activity, whose degradation rate was about three times higher than that of pure BiOBr. The enhanced photocatalytic activity could be attributed to the formation of the BiPO{sub 4}/BiOBr p–n junction, which resulted in the effective separation and transfer of photogenerated electron–hole pairs. Moreover, the trapping experiments confirmed that ·O{sub 2}{sup −} and h{sup +} were the main active species responsible for the degradation of RhB.

  11. Preparation and characterization of Ag{sub 3}PO{sub 4}/BiOI heterostructure photocatalyst with highly visible-light-induced photocatalytic properties

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Yanqin [Institute of Environmental and Chemical Engineering, Jiangsu University of Science and Technology, Zhenjiang 212003, Jiangsu (China); Cheng, Xiaofang [Institute of Environmental and Chemical Engineering, Jiangsu University of Science and Technology, Zhenjiang 212003, Jiangsu (China); State Key Lab Pollutant Control & Resource Reuse, School of the Environmental, Nanjing University, Nanjing 210023, Jiangsu (China); Meng, Xiaoting; Feng, Hongwu [Institute of Environmental and Chemical Engineering, Jiangsu University of Science and Technology, Zhenjiang 212003, Jiangsu (China); Yang, Shaogui; Sun, Cheng [State Key Lab Pollutant Control & Resource Reuse, School of the Environmental, Nanjing University, Nanjing 210023, Jiangsu (China)

    2015-05-25

    Highlights: • Ag{sub 3}PO{sub 4}/BiOI heterostructure photocatalysts were synthesized by simple ion exchange deposition method. • Ag{sub 3}PO{sub 4}/BiOI displayed excellent photocatalytic activities for degradation of RhB and MB under visible light. • Ag{sub 3}PO{sub 4}/BiOI displayed higher photocatalytic activity under visible light than pure BiOI and Ag{sub 3}PO{sub 4}. - Abstract: In this study, novel Ag{sub 3}PO{sub 4}/BiOI heterostructure photocatalysts were synthesized by simple ion-exchange deposition method. The as-prepared products were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), energy disperse spectroscopy (EDS), Fourier transform infrared spectrometer (FT-IR) and UV–vis diffuse reflectance spectroscopy (DRS). In the composites, Ag{sub 3}PO{sub 4} particles are deposited on the surface of plates of BiOI. The photocatalytic tests display that the Ag{sub 3}PO{sub 4}/BiOI heterostructures possess a higher rate for degradation of rhodamine B(RhB), methtylene blue(MB) and methyl orange(MO) than the pure BiOI under visible light illumination. The catalytic activity of the composite is greatly influenced by the molar ratio of Ag{sub 3}PO{sub 4}/BiOI, the best visible-light photocatalytic performance was obtained for 2:1-Ag{sub 3}PO{sub 4}/BiOI for RhB and MB degradation and 1:2-Ag{sub 3}PO{sub 4}/BiOI for MO degradation. The results show that the heterostructure construction between Ag{sub 3}PO{sub 4} and BiOI semiconductors plays a very important role in their photocatalytic properties, which has the potential application in solving environmental pollution issues utilizing solar energy effectively.

  12. Graphene oxide wrapped Ag{sub 3}PO{sub 4} sub-microparticles with highly enhanced photocatalytic activity and stability under visible light irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Xiu, Zhiliang [State Key Laboratory of Crystal Materials, Shandong University, Jinan 250100 (China); Shandong Provincial Key Laboratory of Processing and Testing Technology of Glass and Functional Ceramics, Key Laboratory of Amorphous and Polycrystalline Materials, Qilu University of Technology, Jinan 250353 (China); Wu, Yongzhong, E-mail: wuyz@sdu.edu.cn [State Key Laboratory of Crystal Materials, Shandong University, Jinan 250100 (China); Hao, Xiaopeng, E-mail: xphao@sdu.edu.cn [State Key Laboratory of Crystal Materials, Shandong University, Jinan 250100 (China); Lu, Qifang; Liu, Suwen [Shandong Provincial Key Laboratory of Processing and Testing Technology of Glass and Functional Ceramics, Key Laboratory of Amorphous and Polycrystalline Materials, Qilu University of Technology, Jinan 250353 (China)

    2014-11-15

    Highlights: • Graphene oxide wrapped Ag{sub 3}PO{sub 4} sub-microparticles were prepared. • The photocatalytic activity of Ag{sub 3}PO{sub 4} is increased by 6 times by GO wrapping. • The hybrid photocatalysts exhibited excellent stability. - Abstract: Graphene oxide (GO) wrapped Ag{sub 3}PO{sub 4} sub-microparticles were prepared by in situ deposition–precipitation method. By hybridization of Ag{sub 3}PO{sub 4} with GO nanosheets, a 6-fold enhancement in the photodegradation rate toward orange methyl (MO) under visible light irradiation (λ ≥ 420 nm) was observed compared with the pure Ag{sub 3}PO{sub 4} sub-microsparticles. The hybrid photocatalysts also exhibited excellent stability in the successive MO degradation experiments. The highly enhanced photocatalytic activity and stability were mainly attributed to the quick transfer of the photogenerated electrons from Ag{sub 3}PO{sub 4} to GO nanosheets, which could effectively suppress the electron–hole pairs recombination and thus inhibit the photocorrosion of Ag{sub 3}PO{sub 4}. These high-efficient and stable hybrid photocatalysts were expected to show considerable potential applications in wastewater treatment and water splitting.

  13. Degradation of microcystin-LR by highly efficient AgBr/Ag3PO4/TiO2 heterojunction photocatalyst under simulated solar light irradiation

    Science.gov (United States)

    Wang, Xin; Utsumi, Motoo; Yang, Yingnan; Li, Dawei; Zhao, Yingxin; Zhang, Zhenya; Feng, Chuanping; Sugiura, Norio; Cheng, Jay Jiayang

    2015-01-01

    A novel photocatalyst AgBr/Ag3PO4/TiO2 was developed by a simple facile in situ deposition method and used for degradation of mirocystin-LR. TiO2 (P25) as a cost effective chemical was used to improve the stability of AgBr/Ag3PO4 under simulated solar light irradiation. The photocatalytic activity tests for this heterojunction were conducted under simulated solar light irradiation using methyl orange as targeted pollutant. The results indicated that the optimal Ag to Ti molar ratio for the photocatalytic activity of the resulting heterojunction AgBr/Ag3PO4/TiO2 was 1.5 (named as 1.5 BrPTi), which possessed higher photocatalytic capacity than AgBr/Ag3PO4. The 1.5 BrPTi heterojunction was also more stable than AgBr/Ag3PO4 in photocatalysis. This highly efficient and relatively stable photocatalyst was further tested for degradation of the hepatotoxin microcystin-LR (MC-LR). The results suggested that MC-LR was much more easily degraded by 1.5 BrPTi than by AgBr/Ag3PO4. The quenching effects of different scavengers proved that reactive h+ and •OH played important roles for MC-LR degradation.

  14. Tunable color emission in K3Gd(PO4)2:Tb3+,Sm3+ phosphor for n-UV white light emitting diodes

    Institute of Scientific and Technical Information of China (English)

    王婷; 徐旭辉; 周大成; 邱建备; 余雪

    2015-01-01

    A series of K3Gd(PO4)2:Tb3+,Sm3+ phosphors were synthesized through solid state reaction. By co-doping Tb3+ and Sm3+ into K3Gd(PO4)2 host and singly varying the doping concentration of Sm3+, tunable colors from green to yellow and then to orange were obtained in K3Gd(PO4)2:Tb3+,Sm3+ phosphors under the excitation at 373 nm. The energy transfer process fromTb3+ to Sm3+was verified through luminescence spectra and fluorescence decay curves. Moreover, the energy transfer mechanism was demon-strated to be the quadrupole-quadrupole interaction. The results indicated that K3Gd(PO4)2:Tb3+,Sm3+phosphors could be a potential application for n-UV white light emitting diodes.

  15. Ag(I)-bovine serum albumin hydrosol-mediated formation of Ag3PO4/reduced graphene oxide composites for visible-light degradation of Rhodamine B solution.

    Science.gov (United States)

    Ma, Peiyan; Chen, Anliang; Wu, Yan; Fu, Zhengyi; Kong, Wei; Che, Liyuan; Ma, Ruifang

    2014-03-01

    A cost-effective Ag(I)-bovine serum albumin (BSA) supramolecular hydrosol strategy was utilized to assemble Ag3PO4 nanospheres onto reduced graphene oxide (rGO) sheets. The obtained composites were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, atomic force microscopy, X-ray photoelectron spectroscopy, UV-vis absorption spectroscopy and Fourier transform infrared spectroscopy. Compared with the pure Ag3PO4 crystals and Ag3PO4 particles prepared with Ag(I)-BSA hydrosol as precursor, the Ag3PO4/rGO composites obtained with different content of graphene oxide indicated improved visible-light-driven photocatalysis activity for the decomposition of Rhodamine B aqueous solution. The results pointed to the possibility of synthesizing graphene-based photocatalysts by metal ion-BSA hydrosol.

  16. Forest Fires as a Possible Source of Isotopically Light Marine Fe Aerosols

    Science.gov (United States)

    Tegler, L. A.; Sherry, A. M.; Romaniello, S. J.; Anbar, A. D.

    2016-12-01

    Iron (Fe) is an important limiting micronutrient for primary productivity in many high-nutrient, low-chlorophyll (HNLC) regions of the ocean. These marine systems receive a significant fraction of their Fe from atmospheric deposition, which is thought to be dominated by mineral dust with an Fe isotopic composition at or above 0‰. However, Mead et al. (2013) observed isotopically light Fe in marine aerosols smaller than 2.5 μm, which is difficult to reconcile with known sources of marine aerosols. Based on previous experimental work, we hypothesize that biomass burning is the source of isotopically light Fe in atmospheric particles and suggest that biomass burning might represent an underappreciated source of Fe to marine ecosystems. While Guelke et al (2007) demonstrated that Fe in agricultural plants is isotopically light, few studies have examined the Fe isotope composition of naturally occurring forests likely to be a significant source of Fe during forest fires. To address this question, we measured the isotopic composition of Ponderosa pine growing in northern Arizona. Ponderosa pine is one the most common forest types in the western US and thus representative of an important North American fire region. Pine needles were chosen because they are susceptible to complete combustion during biomass burning events. To determine the Fe isotopic composition of pine trees, pine needles were sampled at various tree heights. We found that these samples had δ56Fe values between -1.5 and 0‰, indicating that pine needles can be isotopically light compared to local grasses and soil. These results support the hypothesis that biomass burning may contribute isotopically light Fe to marine aerosols.

  17. Synthesis and Characterization of High Efficiency and Stable Spherical Ag3PO4 Visible Light Photocatalyst for the Degradation of Methylene Blue Solutions

    Directory of Open Access Journals (Sweden)

    Liqin Qin

    2015-01-01

    Full Text Available A facile method for the synthesis of Ag3PO4 visible light photocatalyst has been developed to improve the photocatalytic activity and stability. The as-prepared samples are investigated by X-ray powder diffraction, scanning electron microscopy, infrared spectroscopy, photoluminescence (PL spectroscopy, and UV-Vis diffuse reflectance spectroscopy techniques. The results reveal that the prepared Ag3PO4 has cube structure with a band gap of 2.26 eV. The as-prepared samples show higher photocatalytic activity for methylene blue (MB degradation than that of N-TiO2 under visible light irradiation.

  18. Fabrication of novel g-C3N4 nanocrystals decorated Ag3PO4 hybrids: Enhanced charge separation and excellent visible-light driven photocatalytic activity.

    Science.gov (United States)

    Sun, Meng; Zeng, Qi; Zhao, Xia; Shao, Yu; Ji, Pengge; Wang, Changqian; Yan, Tao; Du, Bin

    2017-10-05

    Graphitic carbon nitride (g-C3N4) nanocrystals (NCs) decorated Ag3PO4 hybrids were synthesized by a facile method. The obtained samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), transmission electron microscope (TEM), and UV-vis diffuse reflectance spectra (DRS). The SEM and TEM images showed that the as-prepared Ag3PO4 were composed of particles with diameters of 200-500nm, while the obtained nanocrystalline g-C3N4 were composed of smaller particles with average diameter of 10nm. For nanocrystalline g-C3N4/Ag3PO4 hybrids, the particle surfaces of Ag3PO4 were decorated with numerous g-C3N4 NCs, result in a larger contact area between g-C3N4 and Ag3PO4. The photocatalytic performances were evaluated by decomposing MO, phenol, bisphenol A, and RhB under visible light. Compared with Ag3PO4 and g-C3N4, the g-C3N4/Ag3PO4 hybrid (mass ratio=1:4) exhibited the best activity, which was much higher than that of bulk-g-C3N4/Ag3PO4 composite under the same conditions. The enhanced activities should be mainly ascribed to the enhanced separation efficiency of photo-generated carriers, which was proved by the photoluminescence (PL) spectra measurement. Controlled experiments proved that O2(-) and h(+) played the chief role in the degradation process. A possible Z-scheme degradation mechanism of organic contaminant over g-C3N4/Ag3PO4 hybrid was proposed. Copyright © 2017. Published by Elsevier B.V.

  19. Assessment of trace elements, POPs, (210)Po and stable isotopes ((15)N and (13)C) in a rare filter-feeding shark: The megamouth.

    Science.gov (United States)

    Moura, Jailson Fulgencio de; Merico, Agostino; Montone, Rosalinda Carmela; Silva, Josilene; Seixas, Tércia Guedes; Godoy, José Marcus de Oliveira; Saint'Pierre, Tatiana Dillenburg; Hauser-Davis, Rachel Ann; Di Beneditto, Ana Paula Madeira; Reis, Estéfane Cardinot; Tavares, Davi Castro; Lemos, Leila Soledade; Siciliano, Salvatore

    2015-06-15

    With less than 60 records being reported worldwide, the megamouth (Megachasma pelagios) is today one of the least known shark species inhabiting our oceans. Therefore, information concerning the biology and ecology of this enigmatic organism is very scarce and limited to feeding behaviour and preferred habitat. The present work reports new data on the concentrations of trace elements, organic mercury, POPs and (210)Po in hepatic and muscular tissues of a specimen found stranded in the southeastern coast of Brazil. Additionally, we provide new evidence based on stable isotope analysis (δ(15)N and δ(13)C) confirming the preference for the pelagic habitat and the zooplanktivorous feeding behaviour of the megamouth. These results are consistent with the low concentrations of organic pollutant compounds and other elements measured in our samples.

  20. Polonium (²¹⁰Po), uranium (²³⁴U, ²³⁸U) isotopes and trace metals in mosses from Sobieszewo Island, northern Poland.

    Science.gov (United States)

    Boryło, Alicja; Nowicki, Waldemar; Olszewski, Grzegorz; Skwarzec, Bogdan

    2012-01-01

    The activity of polonium (210)Po and uranium (234)U, (238)U radionuclides, as well as trace metals in mosses, collected from Sobieszewo Island area (northern Poland), were determined using the alpha spectrometry, AAS (atomic absorption spectrometry) and OES-ICP (atomic emission spectrometry with inductively coupled plasma). The concentrations of mercury (directly from the solid sample) were determined by the cold vapor technique of CV AAS. The obtained results revealed that the concentrations of (210)Po, (234)U, and (238)U in the two analyzed kinds of mosses: schrebers big red stem moss (Pleurozium schreberi) and broom moss (Dicranum scoparium) were similar. The higher polonium concentrations were found in broom moss (Dicranum scoparium), but uranium concentrations were relatively low for both species of analyzed mosses. Among the analyzed trace metals the highest concentration in mosses was recorded for iron, while the lowest for nickel, cadmium and mercury. The obtained studies showed that the sources of polonium and uranium isotopes, as well as trace metals in analyzed mosses are air city contaminations transported from Gdańsk and from existing in the vicinity the phosphogypsum waste heap in Wiślinka (near Gdańsk).

  1. Developing Potential New Reference Materials for Light Isotopes in Foodstuffs

    Science.gov (United States)

    Frew, Russell; Van Hale, Robert; Clarke, Dianne; Abrahim, Aiman; Resch, Christian; Mayr, Leopold; Cannavan, Andrew; Gröning, Manfred

    2013-04-01

    Measurements of subtle variations in stable isotope ratios provide the means for verifying food integrity in numerous ways. Adulterants usually have different isotopic composition so their presence in a food is readily detectable. Stable isotope measurements can also be used to determine the region of production of the food. In most cases the ability of stable isotope measurements to verify, or otherwise reject, the authenticity of the food is greatly enhanced by comparison of a result to a reference database. The more high-quality data in the database, the more statistical power is afforded by the comparison. A serious weakness at present is the lack of reference materials in food matrices available to the community. Thus researchers have to rely on in-house standards for calibration and quality assurance. The result is that there are numerous datasets published that may be internally consistent but it is exceedingly difficult to combine these datasets into a cohesive database. This is particularly important for measurements of the hydrogen isotopes. Here we present a survey of the stable isotope (^2H, ^13C and ^15N) composition of 12 Reference Materials from the International Atomic Energy Agency catalogue. All but one of these materials are plant matter and have been developed as reference materials for other applications such as radionuclide or trace element measurements. Thus they have been verified as suitable materials in terms of stability and homogeneity for those tests. The purpose of this work is to ascertain if they are similarly suitable as stable isotope reference materials. The results from our survey show that there is a wide range in elemental and isotopic composition among these materials. For example, the ^15N values range from-13.5‰ to +18.6‰ and the nitrogen elemental composition range is from 0.7% to 9.7%. The ^13C values range from -20‰ to -40‰ and the carbon elemental composition ranges from 15% to 47%. We are now in the process of

  2. Chlorine isotope and Cl-Br fractionation in fluids of Poás volcano (Costa Rica): Insight into an active volcanic-hydrothermal system

    Science.gov (United States)

    Rodríguez, Alejandro; Eggenkamp, H. G. M.; Martínez-Cruz, María; van Bergen, Manfred J.

    2016-10-01

    Halogen-rich volcanic fluids issued at the surface carry information on properties and processes operating in shallow hydrothermal systems. This paper reports a long-term record of Cl-Br concentrations and δ37Cl signatures of lake water and fumaroles from the active crater of Poás volcano (Costa Rica), where surface expressions of magmatic-hydrothermal activity have shown substantial periodic changes over the last decades. Both the hyperacid water of its crater lake (Laguna Caliente) and subaerial fumaroles show significant temporal variability in Cl-Br concentrations, Br/Cl ratios and δ37Cl, reflecting variations in the mode and magnitude of volatile transfer. The δ37Cl signatures of the lake, covering the period 1985-2012, show fluctuations between + 0.02 ± 0.06‰ and + 1.15 ± 0.09‰. Condensate samples from adjacent fumaroles on the southern shore, collected during the interval (2010-2012) with strong changes in gas temperature (107-763°C), display a much larger range from - 0.43 ± 0.09‰ to + 14.09 ± 0.08‰. Most of the variations in Cl isotope, Br/Cl and concentration signals can be attributed to interaction between magma-derived gas and liquid water in the volcanic-hydrothermal system below the crater. The δ37Cl were lowest and closest to magmatic values in (1) fumarolic gas that experienced little or no interaction with subsurface water and followed a relatively dry pathway, and (2) water that captured the bulk of magmatic halogen output so that no phase separation could induce fractionation. In contrast, elevated δ37Cl can be explained by partial scavenging and fractionation during subsurface gas-liquid interaction. Hence, strong Cl isotope fractionation leading to very high δ37Cl in Poás' fumaroles indicates that they followed a wet pathway. Highest δ37Cl values in the lake water were found mostly in periods when it received a significant input from subaqueous fumaroles or when high temperatures and low pH caused HCl evaporation. It is

  3. The CeO{sub 2}/Ag{sub 3}PO{sub 4} photocatalyst with stability and high photocatalytic activity under visible light irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Song, Yanhua [School of Environmental and Chemical Engineering, Jiangsu University of Science and Technology, Zhenjiang, 212003 (China); Zhao, Haozhu; Chen, Zhigang; Huang, Liying; Xu, Hui; Li, Huaming [School of the Environment, Institute for Energy Research, Jiangsu University, Zhenjiang, 212013 (China); Wang, Weiren [Department of Chemistry, Rice University, Houston, Texas, 77005 (United States)

    2016-09-15

    The CeO{sub 2}/Ag{sub 3}PO{sub 4} composite photocatalysts are synthesized by an in situ precipitation method. The XRD, FT-IR, XPS, TEM, EDS, and DRS are used to characterize the structure of the samples. The photocatalytic performance of the prepared samples is evaluated by the photocatalytic degradation of methylene blue (MB), rhodamine B (RhB), and ciprofloxacin (CIP). The results show that CeO{sub 2}/Ag{sub 3}PO{sub 4} hybrid materials exhibit much higher photocatalytic activity than the Ag{sub 3}PO{sub 4} alone. The optimal CeO{sub 2} content in CeO{sub 2}/Ag{sub 3}PO{sub 4} composites is found to be molar ratio 1 wt%. Photocurrent response of CeO{sub 2}/Ag{sub 3}PO{sub 4} (1 wt%) is about 1.5 times as high as that of the pure Ag{sub 3}PO{sub 4}. The increase of photocatalytic activity of CeO{sub 2}/Ag{sub 3}PO{sub 4} composites could be mainly attributed to the heterojunction between CeO{sub 2} and Ag{sub 3}PO{sub 4}. The trapping experiment has demonstrated that holes serve as the main active species for the degradation of MB under visible light irradiation. A photocatalytic mechanism is also proposed. (copyright 2016 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  4. Enhancement of the luminescence properties of Sr3 (PO4 )2 :Dy(3+) ,Li(+) white-light-emitting phosphors by charge compensator Li(+) co-doping.

    Science.gov (United States)

    Li, Yuhang; Dai, Siyi; Zhang, Wentao; Zhang, Peicong; Qiu, Kehui

    2017-09-08

    Sr3 (PO4 )2 :Dy(3+) ,Li(+) phosphors were prepared using a simple high temperature solid method for luminescence enhancement. The structures of the as-prepared samples agreed well with the standard phase of Sr3 (PO4 )2 , even when Dy(3+) and Li(+) were introduced. Under ultraviolet excitation at 350 nm, the Sr3 (PO4 )2 :Dy(3+) sample exhibited two emission peaks at 483 nm and 580 nm, which were due to the (4) F9/2  → (6) H15/2 and (4) F9/2  → (6) H13/2 transitions of Dy(3+) ions, respectively. A white light was fabricated using these two emissions from the Sr3 (PO4 )2 :Dy(3+) phosphors. The luminescence properties of Sr3 (PO4 )2 :Dy(3+) ,Li(+) phosphors, including emission intensity and decay time, were improved remarkably with the addition of Li(+) as the charge compensator, which would promote their application in near-ultraviolet excited white-light-emitting diodes. Copyright © 2017 John Wiley & Sons, Ltd.

  5. Visible light driven Ag/Ag{sub 3}PO{sub 4}/AC photocatalyst with highly enhanced photodegradation of tetracycline antibiotics

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Huiqin [School of Materials Science & Engineering, Jiangsu University, Zhenjiang 212013 (China); Ye, Zhefei [School of Chemistry & Chemical Engineering, Jiangsu University, Zhenjiang 212013 (China); Liu, Chun [Jingjiang College of Jiangsu University, Zhenjiang 212013 (China); Li, Jinze; Zhou, Mingjun [School of Chemistry & Chemical Engineering, Jiangsu University, Zhenjiang 212013 (China); Guan, Qingfeng, E-mail: guanqf@mail.ujs.edu.cn [School of Materials Science & Engineering, Jiangsu University, Zhenjiang 212013 (China); Lv, Peng [School of Materials Science & Engineering, Jiangsu University, Zhenjiang 212013 (China); Huo, Pengwei, E-mail: huopw1@163.com [School of Chemistry & Chemical Engineering, Jiangsu University, Zhenjiang 212013 (China); Yan, Yongsheng [School of Chemistry & Chemical Engineering, Jiangsu University, Zhenjiang 212013 (China)

    2015-10-30

    Graphical abstract: - Highlights: • Ag/Ag{sub 3}PO{sub 4}/AC composite photocatalysts were successfully synthesized using the simple deposition and photoinduced methods. • The composite photocatalysts exhibited strong absorption ability in the visible light range. • The photocatalytic mechanism of degradation TC revealed that there were multiple active species in the photocatalytic reactions. - Abstract: Ag/Ag{sub 3}PO{sub 4}/active carbon (AC) composite photocatalysts were successfully synthesized using the simple deposition and photoinduced methods. The structures, morphology and photocatalytic properties of as-prepared photocatalysts were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), diffuse reflectance spectroscopy (DRS), photoluminescence (PL) spectroscopy, X-ray photoelectron spectroscopy (XPS). The Ag/Ag{sub 3}PO{sub 4}/AC composite photocatalysts exhibited a conspicuously improved photocatalytic performance for tetracycline (TC) degradation. The optimal conditions of loaded dosage and photoinduced time were investigated, and the results showed that the photoinduced time played an important role in prepared processes, and also that for the loaded dosage of Ag{sub 3}PO{sub 4}. The DRS analysis showed that the composite photocatalysts exhibited strong absorption ability in the visible light range. The radicals trap experiments demonstrated that there were multiple active species during the degrading process of TC. The possible mechanism of improved photocatalytic activity of Ag–Ag{sub 3}PO{sub 4}/AC composite was also proposed.

  6. Synthesis of magnetically separable Ag3PO4/TiO2/Fe3O4 heterostructure with enhanced photocatalytic performance under visible light for photoinactivation of bacteria.

    Science.gov (United States)

    Xu, Jing-Wen; Gao, Zhi-Da; Han, Kun; Liu, Yongmin; Song, Yan-Yan

    2014-09-10

    Silver orthophosphate (Ag3PO4) is a low-band-gap photocatalyst that has received considerable research interest in recent years. In this work, the magnetic Ag3PO4/TiO2/Fe3O4 heterostructured nanocomposite was synthesized. The nanocomposite was found to exhibit markedly enhanced photocatalytic activity, cycling stability, and long-term durability in the photodegradation of acid orange 7 (AO7) under visible light. Moreover, the antibacterial film prepared from Ag3PO4/TiO2/Fe3O4 nanocomposite presented excellent bactericidal activity and recyclability toward Escherichia coli (E. coli) cells under visible-light irradiation. In addition to the intrinsic cytotoxicity of silver ions, the elevated bactericidal efficiency of Ag3PO4/TiO2/Fe3O4 can be largely attributed to its highly enhanced photocatalytic activity. The photogenerated hydroxyl radicals and superoxide ions on the formed Ag/Ag3PO4/TiO2 interfaces cause considerable morphological changes in the microorganism's cells and lead to the death of the bacteria.

  7. One-pot synthesis of visible-light-driven Ag/Ag3PO4 photocatalyst immobilized on exfoliated montmorillonite by clay-mediated in situ reduction

    Science.gov (United States)

    Liu, Chang; Zhang, Xiaoyuan; Wu, Jianning; Meng, Guihua; Guo, Xuhong; Liu, Zhiyong

    2016-11-01

    In order to find efficient photocatalytic materials and convenient preparation method, a well-designed Ag/Ag3PO4-OMMT (organically modified montmorillonite) plasmonic photocatalyst was synthesized via the "one-pot" process without any reducing species. Ag+ could be reduced by Si-OH moiety on the surface of OMMT. The resulting samples were thoroughly studied by using X-ray diffraction, X-ray photoelectron spectra, transmission electron microscopy, scanning electron microscope, energy-dispersive X-ray spectroscopy, UV-Vis diffuse reflectance spectra, and so on. The as-prepared Ag/Ag3PO4-OMMT photocatalyst exhibited efficient, stable photocatalytic activity and recyclability for the degradation of Rhodamine B (RhB) under visible light radiation ( λ > 420 nm). The optimum synergetic effect of Ag3PO4/OMMT was found at a weight ratio of 50 %. The degradation efficiency of RhB over Ag/Ag3PO4-OMMT (1:1) was about 92.9 %, and photocatalytic activity remained stable after three cycles. The results show that the designed photocatalyst is feasible and effective. The proposed photocatalysis mechanism is probably attributed to surface plasmon resonance of metallic Ag nanoparticles (NPs) and also attributed to negatively charged exfoliated montmorillonite. The Ag/Ag3PO4-OMMT composites showed highly visible light photocatalytic activity, which makes them promising nanomaterials for further applications in water treatment.

  8. Inner Radiation Belt Generation of Light Nuclei Isotope

    Science.gov (United States)

    Galper, A. M.; Koldashov, S. V.; Leonv, A. A.; Mikhailov, V. V.

    2003-07-01

    Nuclear interactions between inner zone protons and atoms in the upper atmosphere provide the essential source of H and He isotop es nuclei in radiation belt. This paper reports the calculations of these isotop es intensities from the inner zone proton intensity model AP-8, the atmosphere drift-averaged composition and densities model MSIS-90, and cross sections for the various interaction processes. To calculate drift-averaged densities and energy losses of secondaries the particles are traced in geomagnetic field according IGRF-95 model by numerical solution of motion equation. The calculations account for nuclear interactions kinematic along the whole trapped protons trajectories. The results of calculations are compared with experimental data from SAMPEX, CRRES, RESURS-04 and MITA satellites taken during different solar activity phases. The comparison with observational data shows that the atmosphere is sufficient source for inner zone 4 He, 3 He,2 H and 3 H for L-shell less than 1.3.

  9. Visible light responsive porous Lanthanum-doped Ag3PO4 photocatalyst with high photocatalytic water oxidation activity.

    Science.gov (United States)

    Xie, Ying Peng; Wang, Guo Sheng

    2014-09-15

    This paper report a facile route of synthesizing Ag3PO4 crystal with smooth surface, and La-doped Ag3PO4 crystal with porous surface by accurately controlling the kinetic parameters during chemical precipitation process. As a result of surface modification induced by La doping, the La-doped Ag3PO4 crystal shows a higher photocatalytic activity than Ag3PO4 crystal in O2 evolution from water splitting. The improved photocatalytic activity of La-doped Ag3PO4 is attributed to the synergistic effects of porous surface structure, abundant surface defects and increased surface area. The result also shows that La doping concentration has a remarkable effect on the photocatalytic activity of Ag3PO4.

  10. Facile synthesis of MWCNTs/Ag{sub 3}PO{sub 4}: novel photocatalysts with enhanced photocatalytic activity under visible light

    Energy Technology Data Exchange (ETDEWEB)

    Tian Jingqi; Li Haiyan; Xing Zhicai; Wang Lei [Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, State Key Lab of Electroanalytical Chemistry (China); Asiri, Abdullah M.; Al-Youbi, Abdulrahman O. [Faculty of Science, King Abdulaziz University, Chemistry Department (Saudi Arabia); Sun, Xuping, E-mail: sunxp@ciac.jl.cn [Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, State Key Lab of Electroanalytical Chemistry (China)

    2013-03-15

    The present communication demonstrates a facile strategy toward rapid in situ synthesis of Ag{sub 3}PO{sub 4} nanoparticles onto the surface of multi-walled carbon nanotubes (MWCNTs/Ag{sub 3}PO{sub 4}) by adding Na{sub 2}HPO{sub 4} into the mixture of MWCNTs and AgNO{sub 3} ethylene glycol solution under stirring. We further demonstrate the use of such composites as novel photocatalysts toward photodecomposition of rhodamine B under visible light. It suggests that varied loading of MWCNTs in the composites has significant influence on the photocatalytic activity and the MWCNTs{sub 2.5%}/Ag{sub 3}PO{sub 4} exhibits the highest photocatalytic performance.Graphical abstract.

  11. Muon capture on light isotopes in Double Chooz

    CERN Document Server

    Abe, Y; Almazan, H; Alt, C; Appel, S; Barriere, J C; Baussan, E; Bekman, I; Bergevin, M; Bezerra, T J C; Bezrukov, L; Blucher, E; Brugière, T; Buck, C; Busenitz, J; Cabrera, A; Camilleri, L; Carr, R; Cerrada, M; Chauveau, E; Chimenti, P; Collin, A P; Conover, E; Conrad, J M; Crespo-Anadón, J I; Crum, K; Cucoanes, A S; Damon, E; Dawson, J V; de Kerret, H; Dhooghe, J; Dietrich, D; Djurcic, Z; Anjos, J C dos; Dracos, M; Etenko, A; Fallot, M; Felde, J; Fernandes, S M; Fischer, V; Franco, D; Franke, M; Furuta, H; Gil-Botella, I; Giot, L; Göger-Neff, M; Gomez, H; Gonzalez, L F G; Goodenough, L; Goodman, M C; Haag, N; Hara, T; Haser, J; Hellwig, D; Hofmann, M; Horton-Smith, G A; Hourlier, A; Ishitsuka, M; Jochum, J; Jollet, C; Kaether, F; Kalousis, L N; Kamyshkov, Y; Kaneda, M; Kaplan, D M; Kawasaki, T; Kemp, E; Kryn, D; Kuze, M; Lachenmaier, T; Lane, C E; Lasserre, T; Letourneau, A; Lhuillier, D; Lima, H P; Lindner, M; López-Castaño, J M; LoSecco, J M; Lubsandorzhiev, B; Lucht, S; Maeda, J; Mariani, C; Maricic, J; Martino, J; Matsubara, T; Mention, G; Meregaglia, A; Miletic, T; Milincic, R; Minotti, A; Nagasaka, Y; Navas-Nicolás, D; Novella, P; Oberauer, L; Obolensky, M; Onillon, A; Osborn, A; Palomares, C; Pepe, I M; Perasso, S; Porta, A; Pronost, G; Reichenbacher, J; Reinhold, B; Röhling, M; Roncin, R; Rybolt, B; Sakamoto, Y; Santorelli, R; Schilithz, A C; Schönert, S; Schoppmann, S; Shaevitz, M H; Sharankova, R; Shrestha, D; Sibille, V; Sinev, V; Skorokhvatov, M; Smith, E; Soiron, M; Spitz, J; Stahl, A; Stancu, I; Stokes, L F F; Strait, M; Suekane, F; Sukhotin, S; Sumiyoshi, T; Sun, Y; Svoboda, R; Terao, K; Tonazzo, A; Thi, H H Trinh; Valdiviesso, G; Vassilopoulos, N; Veyssiere, C; Vivier, M; von Feilitzsch, F; Wagner, S; Walsh, N; Watanabe, H; Wiebusch, C; Wurm, M; Yang, G; Yermia, F; Zimmer, V

    2015-01-01

    Using the Double Chooz detector, designed to measure the neutrino mixing angle $\\theta_{13}$, the products of $\\mu^-$ capture on $^{12}$C, $^{13}$C, $^{14}$N and $^{16}$O have been measured. Over a period of 489.5 days, $2.3\\times10^6$ stopping cosmic $\\mu^-$ have been collected, of which $1.8\\times10^5$ captured on carbon, nitrogen, or oxygen nuclei in the inner detector scintillator or acrylic vessels. The resulting isotopes were tagged using prompt neutron emission (when applicable), the subsequent beta decays, and, in some cases, $\\beta$-delayed neutrons. The most precise measurement of the rate of $^{12}\\mathrm C(\\mu^-,\

  12. Eu(2+)-activated Sr8ZnSc(PO4)7: a novel near-ultraviolet converting yellow-emitting phosphor for white light-emitting diodes.

    Science.gov (United States)

    Huang, Chien-Hao; Chiu, Yi-Chen; Yeh, Yao-Tsung; Chan, Ting-Shan; Chen, Teng-Ming

    2012-12-01

    The crystal structure of Eu(2+)-activated Sr(8)ZnSc(PO(4))(7):Eu(2+) phosphor was refined and determined from XRD profiles by the Rietveld refinement method using a synchrotron light source. This phosphor crystallizes in the monoclinic structure with the I2/a space group. The SZSP:xEu(2+) phosphors showed a broad yellow emission band centered at 511 and 571 nm depending on the concentration of Eu(2+), and the composition-optimized concentration of Eu(2+) in the Sr(8)ZnSc(PO(4))(7):Eu(2+) phosphor was determined to be 2 mol %. The estimated crystal-field splitting and CIE chromaticity coordinates of Sr(8)ZnSc(PO(4))(7):xEu(2+) (x = 0.001-0.05 mol) were 20181-20983 cm(-1) and (0.3835, 0.5074) to (0.4221, 0.5012), respectively, and the emission band showed a redshift from 547 to 571 nm with increasing Eu(2+) concentration. The nonradiative transitions between the Eu(2+) ions in the Sr(8)ZnSc(PO(4))(7) host were attributable to dipole-dipole interactions, and the critical distance was approximately 19.8 Å. The combination of a 400 nm NUV chip with a blend of Sr(8)ZnSc(PO(4))(7):0.02Eu(2+) and BAM:Eu(2+) phosphors (light converters) gave high color rendering indices between 79.38 and 92.88, correlated color temperatures between 4325 and 7937 K, and tuned CIE chromaticity coordinates in the range (0.381, 0.435) to (0.294, 0.310), respectively, depending on the SZSP:0.02Eu(2+)/BAM:Eu(2+) weight ratio. These results suggest that the Sr(8)ZnSc(PO(4))(7):0.02Eu(2+)/BAM:Eu(2+) phosphor blend has potential applications in white NUV LEDs.

  13. Hierarchical Fe3O4@MoS2/Ag3PO4 magnetic nanocomposites: Enhanced and stable photocatalytic performance for water purification under visible light irradiation

    Science.gov (United States)

    Guo, Na; Li, Haiyan; Xu, Xingjian; Yu, Hongwen

    2016-12-01

    Novel hierarchical Fe3O4@MoS2/Ag3PO4 magnetic nanophotocatalyst with remarkable photocatalytic capability were prepared by simply depositing the Ag3PO4 onto the surface of crumpled Fe3O4@MoS2 nanosphere. The nanocomposites were characterized by XRD, TEM, HRTEM, XPS, BET, and UV-vis DRS. The outcome of the photocatalytic experiments demonstrated that Fe3O4@MoS2/Ag3PO4 with 6 wt% content of Ag3PO4 (FM/A-6%) showed the highest photocatalytic activity upon the degradation Congo red (CR) and Rhodamine B (RhB) under both visible light and simulated sunlight irradiation. In addition, FM/A-6% possessed larger specific surface area (76.56 m2/g) and excellent optical property. The possible Z-scheme charge carriers transfer mechanism for the enhanced photocatalytic properties of the FM/A-6% was also discussed. The Z-scheme charge carriers transfer mechanism established between MoS2 and Ag3PO4 facilitate the charge separation efficiency. Moreover, FM/A-6% can be separated and collected easily by external magnetic field and maintain high activity after five times photoreaction cycles. Given the remarkable photocatalytic performance and high stability of FM/A-6% nanocomposite, it is looking forward to exhibit great potential for applications in water purification.

  14. Degradation of Levofloxacin Lactate Using Ag/Ag3PO4 Under Visible Light%Ag/Ag3PO4光催化降解乳酸左氧氟沙星

    Institute of Scientific and Technical Information of China (English)

    徐秀泉; 于小凤; 唐燕; 吴春笃

    2012-01-01

    以AgNO3和Na2HPO4为原料,采用离子交换和超声辅助光致还原法制备具有可见光响应的高活性光催化剂Ag/Ag3PO4。采用X射线衍射、扫描电子显微镜、紫外—可见漫反射光谱等手段对其进行表征。以乳酸左氧氟沙星为模拟自然水体中残留的抗菌药物对光催化剂的性能进行了测定,考查了溶液初始pH值、乳酸左氧氟沙星初始浓度、催化剂用量、自由基清除剂对光催化效果的影响。结果表明:Ag/Ag3PO4光催化剂对乳酸左氧氟沙星表现出较强的光降解能力,当溶液pH=7、Ag/Ag3PO4用量为75mg、500W的可见光照射15min时,对初始浓度为30μmol/L乳酸左氧氟沙星降解率达到93.5%;循环使用4次后,光催化能力没有显著降低。电子空穴(h+)和超氧阴离子自由基(O2)在光催化降解乳酸左氧氟沙星过程中起主要作用。%A visible-light response photocatalyst Ag/Ag3PO4 was prepared by an ion-exchange process between AgNO3 and Na2HPOa and subsequently by ultrasonic-assisted light-induced reduction method and characterized via the X-ray diffraction, scanning electron microscopy and ultraviolet-visible diffuse reflectance spectroscopy. The degradation rate of levofloxacin lactate by photocatalyst Ag/Ag3PO4 was determined using levofloxacin lactate antimicrobial drug residues in waste water as simulation object. The effect of initial of pH value of the solution, concentration of levofloxacin lactate, catalyst dosage on the degradation of levofloxacin lactate was investigated. The photocatalytic results showed that the Ag/Ag3PO4 could degrade levofloxacin lactate efficiently and remained good photocatalytic activity after four times of cycle experiments. The Ag/Ag3PO4 photocatalyst could degrade levofloxacin lactate up to 93.5% under illumination with 500 W visible lights for 15 min when the contents of photocatalyst and levofloxacin lactate were 75 mg, 30 μmol/L respectively and p

  15. Sr9Mg(1.5)(PO4)7:Eu(2+): A Novel Broadband Orange-Yellow-Emitting Phosphor for Blue Light-Excited Warm White LEDs.

    Science.gov (United States)

    Sun, Wenzhi; Jia, Yonglei; Pang, Ran; Li, Haifeng; Ma, Tengfei; Li, Da; Fu, Jipeng; Zhang, Su; Jiang, Lihong; Li, Chengyu

    2015-11-18

    A new orange-yellow-emitting Sr9Mg(1.5)(PO4)7:Eu(2+) phosphor was prepared via high-temperature solid-state reaction. The structure and optical properties of it were studied systematically. Sr9Mg(1.5)(PO4)7:Eu(2+) can be well-excited by 460 nm blue InGaN chips and exhibit a wide emission band covering from 470 to 850 nm with two main peaks centered at 523 and 620 nm, respectively, which originate from 5d-4f dipole-allowed transitions of Eu(2+) in different crystallographic sites. The sites attribution, concentration quenching, fluorescence decay analysis, and temperature-dependent luminescence properties were investigated in detail. Furthermore, a warm white LED device was fabricated by combining a 460 nm blue InGaN chip with the optimized orange-yellow-emitting Sr9Mg(1.5)(PO4)7:Eu(2+). The color coordinate, correlated color temperature and color rendering index of the fabricated LED device were (0.393, 0.352), 3437 K, and 86.07, respectively. Sr9Mg(1.5)(PO4)7:Eu(2+) has great potential to serve as an attractive candidate in the application of blue light-excited warm white LEDs.

  16. Spectroscopy of $^{194}$Po

    CERN Document Server

    Younes, W; Jin, H Q; Bernstein, L A; McNabb, D P; Davids, C N; Janssens, R V F; Khoo, T L; Lister, C J; Blumenthal, D J; Carpenter, M P; Henderson, D; Henry, R G; Lauritsen, T; Nisius, D T; Pentillä, H; Drigert, M W; Jin, H Q

    1995-01-01

    Prompt, in-beam \\gamma rays following the reaction ^{170}Yb + 142 MeV ^{28}Si were measured at the ATLAS facility using 10 Compton-suppressed Ge detectors and the Fragment Mass Analyzer. Transitions in ^{194}Po were identified and placed using \\gamma-ray singles and coincidence data gated on the mass of the evaporation residues. A level spectrum up to J\\approx10\\hbar was established. The structure of ^{194}Po is more collective than that observed in the heavier polonium isotopes and indicates that the structure has started to evolve towards the more collective nature expected for deformed nuclei.

  17. Evolution of nuclear shape in the light radon isotopes

    CERN Multimedia

    Reiter, P; Blazhev, A A; Kruecken, R; Rahkila, P J; Grahn, T; Wadsworth, R; Gernhaeuser, R A; Bree, N C F; Habs, D; Jenkins, D G; Huyse, M L

    2008-01-01

    We propose to carry out Coulomb excitation of post-accelerated beams of $^{202,204}$ Rn from the REX-ISOLDE facility. The aim of this study is to expand our understanding of nuclear shape coexistence, which has been increasingly well-established in the light mercury and lead nuclei to these very heavy nuclei. Such an extension will provide stringent tests of nuclear models of collectivity and shape coexistence in a previously-inaccessible heavy mass region. REX- ISOLDE is the only facility worldwide at the present time which can provide accelerated beams of such heavy radioactive nuclei.

  18. Visible-light-driven TiO{sub 2}/Ag{sub 3}PO{sub 4}/GO heterostructure photocatalyst with dual-channel for photo-generated charges separation

    Energy Technology Data Exchange (ETDEWEB)

    Lu, Bingqing; Ma, Ni; Wang, Yaping; Qiu, Yiwei [Center for Optoelectronics Materials and Devices, Department of Physics, Zhejiang Sci-Tech University, Hangzhou 310018 (China); Hu, Haihua [Zhejiang University City College, Hangzhou 310015 (China); Zhao, Jiahuan; Liang, Dayu; Xu, Sheng; Li, Xiaoyun; Zhu, Zhiyan [Center for Optoelectronics Materials and Devices, Department of Physics, Zhejiang Sci-Tech University, Hangzhou 310018 (China); Cui, Can, E-mail: cancui@zstu.edu.cn [Center for Optoelectronics Materials and Devices, Department of Physics, Zhejiang Sci-Tech University, Hangzhou 310018 (China)

    2015-05-05

    Highlights: • TiO{sub 2}/Ag{sub 3}PO{sub 4}/GO was synthesized with a facile two-step method. • TiO{sub 2}/Ag{sub 3}PO{sub 4}/GO exhibit superior photocatalytic activity and stability. • TiO{sub 2}/Ag{sub 3}PO{sub 4}/GO has dual-channel for photo-generated charges separation. • TiO{sub 2}/Ag{sub 3}PO{sub 4}/GO composite reduces the consumption of Ag. - Abstract: A novel triple-component TiO{sub 2}/Ag{sub 3}PO{sub 4}/graphene oxide (TiO{sub 2}/Ag{sub 3}PO{sub 4}/GO) photocatalyst with dual channels for photo-generated charges separation has been synthesized to improve the photocatalytic activity and stability of Ag{sub 3}PO{sub 4} under visible light. The synthesis involved in-situ growth of Ag{sub 3}PO{sub 4} nanoparticles on GO sheets to form Ag{sub 3}PO{sub 4}/GO, and then deposited TiO{sub 2} nanocrystals on the surface of Ag{sub 3}PO{sub 4} by hydrolysis of Ti(SO{sub 4}){sub 2} at low-temperature hydrothermal condition. The TiO{sub 2}/Ag{sub 3}PO{sub 4}/GO exhibited superior photocatalytic activity and stability to bare Ag{sub 3}PO{sub 4}, TiO{sub 2}/Ag{sub 3}PO{sub 4} and Ag{sub 3}PO{sub 4}/GO in degradation of Rhodamine B and phenol solutions under visible light. It is suggested that the photo-generated electrons in the conduction band of Ag{sub 3}PO{sub 4} can be quickly transferred to GO, while the holes in the valence band of Ag{sub 3}PO{sub 4} can be transferred to the valence band of TiO{sub 2}. The dual transfer channels at the interfaces of TiO{sub 2}/Ag{sub 3}PO{sub 4}/GO result in effective charges separation, leading to enhanced photocatalytic activity and stability. Furthermore, the content of noble metal Ag significantly reduces from 77 wt% in bare Ag{sub 3}PO{sub 4} to 55 wt% in the nanocomposite. The concept of establishing dual channels for charges separation in a triple-component heterostructure provides a promising way to develop photocatalysts with high efficiency.

  19. Strictly finite range potential for light PET isotopes

    CERN Document Server

    Salamon, P; Balkay, L

    2012-01-01

    By adjusting the parameters of the new phenomenological nuclear potential introduced recently by P. Salamon and T. Vertse (2008) (SV) to the global potential sets of Perey and of Becchetti and Greenlees, it is shown that the SV potential well approximates the cut-off Woods--Saxon (CWS) form even if its second term is set to zero. The important difference between the CWS and SV potentials is that CWS jumps to zero at the cut-off radius, while the SV potential goes to zero smoothly. We fitted the single-term SV potential to the global potentials, and compared the spectra and the pole trajectories of neutron single-particle states generated by some light neutron-deficient nuclei that are most often used in positron emission tomography (PET): $^{13}$N, $^{15}$O and $^{18}$F. The CWS and the SV energies agree reasonably well, and only the pole trajectories, which span extremities, are substantially different.

  20. Fabrication of a direct Z-scheme type WO3/Ag3PO4 composite photocatalyst with enhanced visible-light photocatalytic performances

    Science.gov (United States)

    Lu, Jinsuo; Wang, Yujing; Liu, Fei; Zhang, Liang; Chai, Shouning

    2017-01-01

    A direct Z-scheme type photocatalyst WO3/Ag3PO4 composite (molar ration 1:1, 1W/1Ag) was prepared by hydrothermal method. The 1W/1Ag was characterized by scanning electron microscopy (SEM), X-ray powder diffraction (XRD), UV-vis diffuse reflection spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), and photoluminescence emission spectroscopy (PL) etc. technologies. The photocatalytic performances were evaluated by degradation of methylene blue (MB) and methyl orange (MO), and their removal rates were up to 95% after 60 min and 90% after 180 min, respectively. The prepared 1W/1Ag exhibits a much higher photocatalytic activity than pure Ag3PO4 and pure WO3 under visible light irradiation. The apparent rate constants of MB and MO degradation on 1W/1Ag are about 2.4 and 2.5 times that of pure Ag3PO4, respectively. The enhanced performance of the 1W/1Ag is attributed to a synergistic effect including relatively high surface area, strong light absorption, matched energy band structure, and the improved separation of photogenerated charge carriers between the two components. A reasonable Z-scheme mechanism referring to directed migration of photoinduced carriers was proposed. Thus, it can be suggested that the 1W/1Ag can serve as a promising photocatalyst for environmental purification and clean energy utilization.

  1. Controlled synthesis of Ag{sub 3}PO{sub 4}/BiVO{sub 4} composites with enhanced visible-light photocatalytic performance for the degradation of RhB and 2, 4-DCP

    Energy Technology Data Exchange (ETDEWEB)

    Qi, Xuemei [School of Chemistry and Chemical Engineering, Shanghai Key Lab of Electrical Insulation and Thermal Aging, Shanghai Jiao Tong University, Shanghai 200240 (China); School of Environmental and Chemical Engineering, Shanghai University of Electric Power, Shanghai 200090 (China); Gu, Miaoli [School of Environmental and Chemical Engineering, Shanghai University of Electric Power, Shanghai 200090 (China); Zhu, Xinyuan [School of Chemistry and Chemical Engineering, Shanghai Key Lab of Electrical Insulation and Thermal Aging, Shanghai Jiao Tong University, Shanghai 200240 (China); Wu, Jiang, E-mail: qixuemei@shiep.edu.cn [School of Energy and Mechanical Engineering, Shanghai University of Electric Power, Shanghai 200090 (China); Wu, Qiang; Long, Huimin; He, Kai [School of Environmental and Chemical Engineering, Shanghai University of Electric Power, Shanghai 200090 (China)

    2016-08-15

    Highlights: • Ag{sub 3}PO{sub 4}/BiVO{sub 4} composites were synthesized by in-situ precipitation method. • Ag{sub 3}PO{sub 4}/BiVO{sub 4} is more efficient than pure Ag{sub 3}PO{sub 4} and BiVO{sub 4} for RhB and 2, 4-DCP degradation. • Ag{sub 3}PO{sub 4}/BiVO{sub 4} can act as a high performance and low cost photocatalyst. - Abstract: Ag{sub 3}PO{sub 4}/BiVO{sub 4} composites were fabricated by in-situ precipitation method. Results showed that Ag{sub 3}PO{sub 4}/BiVO{sub 4} composites exhibited higher photocatalytic activity than that of pure BiVO{sub 4} and Ag{sub 3}PO{sub 4} sample under visible light irradiation. The effect of Ag{sub 3}PO{sub 4}:BiVO{sub 4} ratio on the photocatalytic activity was systemically studied and the optimum molar ratio of Ag{sub 3}PO{sub 4}:BiVO{sub 4} was 1:5. The Ag{sub 3}PO{sub 4}/BiVO{sub 4}-5 exhibited excellent photocatalytic activity for the degradation of Rhodamine B (ca. 92% in 30 min) and 2, 4-dichlorophenol (ca. 84% in 180 min) under visible light irradiation. The enhanced photocatalytic activity could be mainly ascribed to the suitable Ag{sub 3}PO{sub 4}/BiVO{sub 4} heterojunction interface and the smaller particles of Ag{sub 3}PO{sub 4} compared to pure Ag{sub 3}PO{sub 4} particles which could promote the separation of photoinduced electron-hole pairs. The Ag{sub 3}PO{sub 4}/BiVO{sub 4} composite can significantly reduce the silver consumption compared to the pure Ag{sub 3}PO{sub 4}. It is worth noting that Ag{sub 3}PO{sub 4}/BiVO{sub 4} composite can act as a high performance and low cost visible-light-driven photocatalyst for environmental remediation.

  2. Reduced graphene oxide enwrapped pinecone-liked Ag{sub 3}PO{sub 4}/TiO{sub 2} composites with enhanced photocatalytic activity and stability under visible light

    Energy Technology Data Exchange (ETDEWEB)

    Ma, Ni; Qiu, Yiwei; Zhang, Yichao; Liu, Hanyang; Yang, Yana; Wang, Jingwei; Li, Xiaoyun; Cui, Can, E-mail: cancui@zstu.edu.cn

    2015-11-05

    Ag{sub 3}PO{sub 4} possesses high photocatalytic activity under visible light, but its application is limited by photogenerated charges recombination, photocorrosion as well as consumption of noble Ag. It is of great interesting to develop new Ag{sub 3}PO{sub 4}-based photocatalysts with high charges separation efficiency, good stability and low content of Ag. In this paper, we report a novel Ag{sub 3}PO{sub 4}/TiO{sub 2}/reduced graphene oxide (Ag{sub 3}PO{sub 4}/TiO{sub 2}/rGO) photocatalyst. It exhibits advantages on both the microstructure and the charges separation. The microstructure shows that TiO{sub 2} spheres of hundreds of nanometers in size are decorated with dense nano-sized Ag{sub 3}PO{sub 4} to form pinecone-liked particles, which are enwrapped by rGO sheets. This novel structure effectively prevents aggregation of nano-sized Ag{sub 3}PO{sub 4}, which not only suppresses the charges recombination in Ag{sub 3}PO{sub 4} but also significantly reduces the content of Ag. Ag{sub 3}PO{sub 4}/TiO{sub 2}/rGO also favors separation of photogenerated charges owing to its two pathways for charges transportation, i.e., the electrons in Ag{sub 3}PO{sub 4} can be transferred to rGO, while the holes in Ag{sub 3}PO{sub 4} can be transferred to TiO{sub 2}. The dual-pathway for charges separation as well as the pinecone-liked Ag{sub 3}PO{sub 4}/TiO{sub 2} microstructure ultimately leads to enhanced photocatalytic activity and stability of Ag{sub 3}PO{sub 4}/TiO{sub 2}/rGO. The photocatalytic performance varies with different contents of Ag{sub 3}PO{sub 4} in the composites, because low content of Ag{sub 3}PO{sub 4} induces weak light absorption while excess Ag{sub 3}PO{sub 4} results in serious charges recombination due to the aggregation of Ag{sub 3}PO{sub 4} nanoparticles. In this work, Ag{sub 3}PO{sub 4}/TiO{sub 2}/rGO with weight ratio of Ag{sub 3}PO{sub 4} against TiO{sub 2}/rGO equals to 0.6 exhibits the highest photocatalytic activity. The percentage of Ag in

  3. Methane Production Pathways in a California Rice Paddy: Isotopic Evidence for Substantial CO2 Reduction as Cause for Isotopically Light Emitted CH4 Carbon

    Science.gov (United States)

    Tyler, S. C.; McMillan, A. M.; Bearden, K.; Chidthaisong, A.; Macalady, J.

    2003-12-01

    We report measurements of δ 13C of emitted CH4 and sediment CH4 and CO2 during the 1999 rice-growing season near Maxwell, CA. Two treatments, one with rice straw incorporated from the previous season and one without rice straw were studied. The δ 13C value of emitted CH4 was consistently lighter isotopically (-67‰ to -83‰ throughout the season) in both straw incorporated and straw removed (burned) plots than in fields we have studied in Texas, Kenya, and Japan. Measured isotopic values of the production zone CH4 were compared to a two-point mixing curve representative of isotopic CH4 produced from either pure methyl-group fermentation or CO2 reduction pathways to partition the production pathways and to track seasonal changes in the production processes. Our sediment CH4 and CO2 isotope data indicate that fermentation was rarely the dominant methanogenic pathway - on the contrary CO2 reduction with H2 was more prevalent than fermentation methanogenesis throughout most of the season. The relatively isotopically light CH4 emitted by the paddy fields is also a product of oxidation and stem-transport processes which have isotopic effects of their own. These effects are discussed in context with the methanogenic isotope effects to provide a complete picture of the paddy field CH4 carbon isotope system.

  4. ZIRCONIUM—HAFNIUM ISOTOPE EVIDENCE FROM METEORITES FOR THE DECOUPLED SYNTHESIS OF LIGHT AND HEAVY NEUTRON-RICH NUCLEI

    Energy Technology Data Exchange (ETDEWEB)

    Akram, W.; Schönbächler, M. [School of Earth, Atmospheric and Environmental Sciences, The University of Manchester, Oxford Road, Manchester, M13 9PL (United Kingdom); Sprung, P. [Institut für Planetologie, Universität Münster, Wilhelm-Klemm-Strasse 10, D-48149 Münster (Germany); Vogel, N. [Institute for Geochemistry and Petrology, ETH, Clausiusstrasse 25, 8092 Zürich (Switzerland)

    2013-11-10

    Recent work based on analyses of meteorite and terrestrial whole-rock samples showed that the r- and s- process isotopes of Hf were homogeneously distributed throughout the inner solar system. We report new Hf isotope data for Calcium-Aluminum-rich inclusions (CAIs) of the CV3 carbonaceous chondrite Allende, and novel high-precision Zr isotope data for these CAIs and three carbonaceous chondrites (CM, CO, CK). Our Zr data reveal enrichments in the neutron-rich isotope {sup 96}Zr (≤1ε in {sup 96}Zr/{sup 90}Zr) for bulk chondrites and CAIs (∼2ε). Potential isotope effects due to incomplete sample dissolution, galactic and cosmic ray spallation, and the nuclear field shift are assessed and excluded, leading to the conclusion that the {sup 96}Zr isotope variations are of nucleosynthetic origin. The {sup 96}Zr enrichments are coupled with {sup 50}Ti excesses suggesting that both nuclides were produced in the same astrophysical environment. The same CAIs also exhibit deficits in r-process Hf isotopes, which provides strong evidence for a decoupling between the nucleosynthetic processes that produce the light (A ≤ 130) and heavy (A > 130) neutron-rich isotopes. We propose that the light neutron-capture isotopes largely formed in Type II supernovae (SNeII) with higher mass progenitors than the supernovae that produced the heavy r-process isotopes. In the context of our model, the light isotopes (e.g. {sup 96}Zr) are predominantly synthesized via charged-particle reactions in a high entropy wind environment, in which Hf isotopes are not produced. Collectively, our data indicates that CAIs sampled an excess of materials produced in a normal mass (12-25 M{sub ☉}) SNII.

  5. Tuning near-gap electronic structure, interface charge transfer and visible light response of hybrid doped graphene and Ag3PO4 composite: Dopant effects

    CERN Document Server

    He, Chao-Ni; Xu, Liang; Yang, Yin-Cai; Zhou, Bing-Xin; Huang, Gui-Fang; Peng, P; Liu, Wu-Ming

    2015-01-01

    The enhanced photocatalytic performance of doped graphene(GR)/semiconductor nanocomposites have recently been widely observed, but an understanding of the underlying mechanisms behind it is still out of reach. As a model system to study the effect of dopants, we investigate the electronic structures and optical properites of doped GR/Ag3PO4 nanocomposites using the first-principles calculations, demonstrating that the band gap, near-gap electronic structure and interface charge transfer of the doped GR/Ag3PO4(100) composite can be tuned by the dopants. Interestingly, the doping atom and C atoms bonded to dopant become active sites for photocatalysis because they are positively or negatively charged due to the charge redistribution caused by interaction. The dopants can enhance the visible light absorption and photoinduced electrons transfer. We propose that the N atom may be most appropriate doping for the GR/Ag3PO4 photocatalyst. This work can rationalize the available experimental results about N-doped GR-s...

  6. Nuclear charge radii of light isotopes based on frequency comb measurements

    Energy Technology Data Exchange (ETDEWEB)

    Zakova, Monika

    2010-02-11

    Optical frequency comb technology has been used in this work for the first time to investigate the nuclear structure of light radioactive isotopes. Therefore, three laser systems were stabilized with different techniques to accurately known optical frequencies and used in two specialized experiments. Absolute transition frequency measurements of lithium and beryllium isotopes were performed with accuracy on the order of 10{sup -10}. Such a high accuracy is required for the light elements since the nuclear volume effect has only a 10{sup -9} contribution to the total transition frequency. For beryllium, the isotope shift was determined with an accuracy that is sufficient to extract information about the proton distribution inside the nucleus. A Doppler-free two-photon spectroscopy on the stable lithium isotopes {sup 6,7}Li was performed in order to determine the absolute frequency of the 2S {yields} 3S transition. The achieved relative accuracy of 2 x 10{sup -10} is improved by one order of magnitude compared to previous measurements. The results provide an opportunity to determine the nuclear charge radius of the stable and short-lived isotopes in a pure optical way but this requires an improvement of the theoretical calculations by two orders of magnitude. The second experiment presented here was performed at ISOLDE/CERN, where the absolute transition frequencies of the D{sub 1} and D{sub 2} lines in beryllium ions for the isotopes {sup 7,9,10,11}Be were measured with an accuracy of about 1 MHz. Therefore, an advanced collinear laser spectroscopy technique involving two counter-propagating frequency-stabilized laser beams with a known absolute frequency was developed. The extracted isotope shifts were combined with recent accurate mass shift calculations and the root-mean square nuclear charge radii of {sup 7,10}Be and the one-neutron halo nucleus {sup 11}Be were determined. Obtained charge radii are decreasing from {sup 7}Be to {sup 10}Be and increasing again for

  7. Synthesis and luminescence properties of KCaPO4:Eu2+,Tb3+,Mn2+ for white-light-emitting diodes (WLED)

    Institute of Scientific and Technical Information of China (English)

    方宏威; 黄山; 韦先涛; 段昌奎; 尹民; 陈永虎

    2015-01-01

    In order to obtain a single-host white-light phosphor, a series of KCaPO4 powder samples tri-doped with Eu2+, Tb3+ and Mn2+ were synthesized via high-temperature solid-state reaction method. Their structural and luminescence properties were investi-gated. Under proper ultraviolet excitation (255–405 nm), white light was obtained, consisting of blue, green and red emissions stem-ming from Eu2+, Tb3+, Mn2+ ions respectively. The temperature stability of our sample was analyzed by studying the variation ten-dency of CIE chromaticity coordinates at different temperatures. The results indicated that this phosphor could yield good color sta-bility when utilized in WLED.

  8. Ag3PO4/BiVO4复合光催化剂的制备及可见光催化降解染料%Synthesis of Ag3PO4/BiVO4 Composite Photocatalyst and Its Photocatalytic Degradation of Dyes under Visible Light Irradiation

    Institute of Scientific and Technical Information of China (English)

    葛明; 谭勉勉; 崔广华

    2014-01-01

    Silver phosphate/bismuth vanadate (Ag3PO4/BiVO4) composite photocatalysts were successful y synthesized by coupling a reflux method with an in situ precipitation route. X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), energy dispersive X-ray spectroscopy (EDS), UV-Vis diffuse reflectance spectroscopy (DRS), and photoluminescence (PL) spectroscopy were used to characterize the as-prepared products. The XRD and FESEM results showed that Ag3PO4/BiVO4 composite photocatalysts were successful y obtained. An energy-efficient light emitting diode lamp was used as the visible light source, and the photocatalytic performances of the as-synthesized products were evaluated for dye degradation in a low-cost photocatalytic system. The Ag3PO4/BiVO4 composite with a Ag3PO4:BiVO4 molar ratio of 1:3 exhibited much higher photocatalytic activity than pure Ag3PO4 catalyst, resulting in decreased use of Ag3PO4. The Ag3PO4/BiVO4 composite photocatalyst showed the best photoactivity in neutral solution and had a higher photodegradation rate for cationic dyes than anionic dyes. The superoxide radicals (O−2•) and holes (h+) were considered to be the main active species in the Ag3PO4/BiVO4 system. The photocatalytic activity of the Ag3PO4/BiVO4 composite photocatalyst decreased to different degrees after three cycles because of the production of metal ic silver.%结合回流法和原位沉淀法成功制备磷酸银/矾酸铋(Ag3PO4/BiVO4)复合光催化剂。通过X射线衍射(XRD)、场发射扫描电子显微镜(FESEM)、能量色散X射线光谱(EDS)、紫外-可见漫反射光谱(UV-Vis DRS)及光致发光(PL)光谱对制备样品进行表征。 XRD和FESEM结果表明成功制备Ag3PO4/BiVO4复合光催化剂。采用节能发光二极管灯(LED)作为可见光光源,在低消耗光催化系统中评价制备样品可见光催化降解染料的活性。当Ag3PO4和BiVO4的组成摩尔比为1:3时,复合Ag3PO4/BiVO4光催

  9. Production of medical isotopes from a thorium target irradiated by light charged particles up to 70 MeV

    Science.gov (United States)

    Duchemin, C.; Guertin, A.; Haddad, F.; Michel, N.; Métivier, V.

    2015-02-01

    The irradiation of a thorium target by light charged particles (protons and deuterons) leads to the production of several isotopes of medical interest. Direct nuclear reaction allows the production of Protactinium-230 which decays to Uranium-230 the mother nucleus of Thorium-226, a promising isotope for alpha radionuclide therapy. The fission of Thorium-232 produces fragments of interest like Molybdenum-99, Iodine-131 and Cadmium-115g. We focus our study on the production of these isotopes, performing new cross section measurements and calculating production yields. Our new sets of data are compared with the literature and the last version of the TALYS code.

  10. Production of medical isotopes from a thorium target irradiated by light charged particles up to 70 MeV.

    Science.gov (United States)

    Duchemin, C; Guertin, A; Haddad, F; Michel, N; Métivier, V

    2015-02-07

    The irradiation of a thorium target by light charged particles (protons and deuterons) leads to the production of several isotopes of medical interest. Direct nuclear reaction allows the production of Protactinium-230 which decays to Uranium-230 the mother nucleus of Thorium-226, a promising isotope for alpha radionuclide therapy. The fission of Thorium-232 produces fragments of interest like Molybdenum-99, Iodine-131 and Cadmium-115g. We focus our study on the production of these isotopes, performing new cross section measurements and calculating production yields. Our new sets of data are compared with the literature and the last version of the TALYS code.

  11. Degradation of microcystin-LR by highly efficient AgBr/Ag{sub 3}PO{sub 4}/TiO{sub 2} heterojunction photocatalyst under simulated solar light irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Xin [School of Environment and Energy, Shenzhen Graduate School of Peking University, Shenzhen, 518055 (China); Utsumi, Motoo, E-mail: utsumi.motoo.ge@u.tsukuba.ac.jp [Graduate School of Life and Environmental Science, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8572 (Japan); Yang, Yingnan; Li, Dawei [Graduate School of Life and Environmental Science, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8572 (Japan); Zhao, Yingxin [School of Environmental Science and Engineering, Tianjin University, Tianjin, 300072 (China); Zhang, Zhenya [Graduate School of Life and Environmental Science, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8572 (Japan); Feng, Chuanping [School of Water Resource and Environment, China University of Geosciences (Beijing), Beijing, 10083, P.R. China (China); Sugiura, Norio [Graduate School of Life and Environmental Science, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8572 (Japan); Cheng, Jay Jiayang [School of Environment and Energy, Shenzhen Graduate School of Peking University, Shenzhen, 518055 (China)

    2015-01-15

    Highlights: • AgBr/Ag{sub 3}PO{sub 4}/TiO{sub 2} consisting of less silver content possessed much higher photocatalytic activity than AgBr/Ag{sub 3}PO{sub 4}. • Reactive h{sup +} and • OH played the major roles for MC-LR degradation by AgBr/Ag{sub 3}PO{sub 4}/TiO{sub 2}. • AgBr/Ag{sub 3}PO{sub 4}/TiO{sub 2} photocatalyst was more stable than AgBr/Ag{sub 3}PO{sub 4} in successive runs. • MC-LR was degraded into intermediates of smaller molecule weight (m/z < 770) by AgBr/Ag{sub 3}PO{sub 4}/TiO{sub 2.} - Abstract: A novel photocatalyst AgBr/Ag{sub 3}PO{sub 4}/TiO{sub 2} was developed by a simple facile in situ deposition method and used for degradation of mirocystin-LR. TiO{sub 2} (P25) as a cost effective chemical was used to improve the stability of AgBr/Ag{sub 3}PO{sub 4} under simulated solar light irradiation. The photocatalytic activity tests for this heterojunction were conducted under simulated solar light irradiation using methyl orange as targeted pollutant. The results indicated that the optimal Ag to Ti molar ratio for the photocatalytic activity of the resulting heterojunction AgBr/Ag{sub 3}PO{sub 4}/TiO{sub 2} was 1.5 (named as 1.5 BrPTi), which possessed higher photocatalytic capacity than AgBr/Ag{sub 3}PO{sub 4}. The 1.5 BrPTi heterojunction was also more stable than AgBr/Ag{sub 3}PO{sub 4} in photocatalysis. This highly efficient and relatively stable photocatalyst was further tested for degradation of the hepatotoxin microcystin-LR (MC-LR). The results suggested that MC-LR was much more easily degraded by 1.5 BrPTi than by AgBr/Ag{sub 3}PO{sub 4}. The quenching effects of different scavengers proved that reactive h{sup +} and • OH played important roles for MC-LR degradation.

  12. Visible light induced H{sub 2}PO{sub 4}{sup -} removal over CuAlO{sub 2} catalyst

    Energy Technology Data Exchange (ETDEWEB)

    Benreguia, N. [Laboratory of Storage and Valorization of Renewable Energies, Faculty of Chemistry, (U.S.T.H.B), BP 32, 16111 Algiers (Algeria); Omeiri, S. [Laboratory of Storage and Valorization of Renewable Energies, Faculty of Chemistry, (U.S.T.H.B), BP 32, 16111 Algiers (Algeria); Centre of Research in Physical and Chemical analysis (CRAPC), BP 248 Algiers RP 16004, Algiers (Algeria); Bellal, B. [Laboratory of Storage and Valorization of Renewable Energies, Faculty of Chemistry, (U.S.T.H.B), BP 32, 16111 Algiers (Algeria); Trari, M., E-mail: solarchemistry@gmail.com [Laboratory of Storage and Valorization of Renewable Energies, Faculty of Chemistry, (U.S.T.H.B), BP 32, 16111 Algiers (Algeria)

    2011-09-15

    Highlights: {yields} The photoactivity of the delafossite CuAlO{sub 2} is enhanced under mild conditions. {yields} The conduction band of CuAlO{sub 2} is of cationic type, providing a high reducing power. {yields} The photo reduction of phosphate is well described by a first order kinetic. - Abstract: The delafossite CuAlO{sub 2} is successfully used for the visible light driven H{sub 2}PO{sub 4}{sup -} reduction. It is prepared from the nitrates decomposition in order to increase the ratio of reaction surface per given mass. CuAlO{sub 2} is a narrow band gap semiconductor which exhibits a good chemical stability with a corrosion rate of 1.70 {mu}mol year{sup -1} at neutral pH. The flat band potential (+0.25 V{sub SCE}) is determined from the Mott-Schottky characteristic. Hence, the conduction band, positioned at (-1.19 V{sub SCE}), lies below the H{sub 2}PO{sub 4}{sup -} level yielding a spontaneous reduction under visible illumination. The photocatalytic process is investigated under mild conditions and 30% conversion occurs in less than {approx}6 h with a quantum efficiency of {approx}0.04% under full light. The concentration decreases by a factor of 39% after a second cycle. The photoactivity follows a first order kinetic with a rate constant of 6.6 x 10{sup -2} h{sup -1}. The possibility of identifying the reaction products via the intensity-potential characteristics is explored. The decrease of the conversion rate over illumination time is due to the competitive water reduction.

  13. Pressure dependence of the deuterium isotope effect in the photolysis of formaldehyde by ultraviolet light

    Directory of Open Access Journals (Sweden)

    E. J. K. Nilsson

    2010-04-01

    Full Text Available The pressure dependence of the relative photolysis rate of HCHO vs. HCDO has been investigated for the first time, using a photochemical reactor at the University of Copenhagen. The dissociation of HCHO vs. HCDO using a UVA lamp was measured at total bath gas pressures of 50, 200, 400, 600 and 1030 mbar. The products of formaldehyde photodissociation are either H2 + CO (molecular channel or HCO + H (radical channel, and a photolysis lamp was chosen to emit light at wavelengths that greatly favor the molecular channel. The isotope effect in the dissociation, kHCHO/kHCDO, was found to depend strongly on pressure, varying from 1.1 + 0.15/−0.1 at 50 mbar to 1.75±0.10 at 1030 mbar. The results can be corrected for radical channel contribution to yield the kinetic isotope effect for the molecular channel; i.e. the KIE in the production of molecular hydrogen. This is done and the results at 1030 mbar are discussed in relation to previous studies at ambient pressure. In the atmosphere the relative importance of the two product channels changes with altitude as a result of changes in pressure and actinic flux. The study demonstrates that the δD of photochemical hydrogen produced from formaldehyde will increase substantially as pressure decreases.

  14. Vibrational spectra of chemical and isotopic variants of oxyluciferin, the light emitter of firefly bioluminescence.

    Science.gov (United States)

    Maltsev, Oleg V; Yue, Ling; Rebarz, Mateusz; Hintermann, Lukas; Sliwa, Michel; Ruckebusch, Cyril; Pejov, Ljupčo; Liu, Ya-Jun; Naumov, Panče

    2014-08-18

    The chemical complexity of oxyluciferin (OxyLH2), the light-emitting molecule in the bioluminescence of fireflies, originates from the possibility of keto/enol tautomerism and single or double deprotonation. Herein, we present detailed infrared spectroscopic analysis of OxyLH2 and several of its chemical isomers and isotopomers. To facilitate the future characterization of its biogenic forms, we provide accurate assignments of the solid-state and solution FTIR spectra of OxyLH2 based on comparison to six isotopically labeled variants ([2-(13)C]-OxyLH2, [3-(15)N]-OxyLH2, [4-(13)C]-OxyLH2, [5-(13)C]-OxyLH2, [2'-(13)C]-OxyLH2, [3'-(15)N]-OxyLH2), five closely related structural analogues, and theoretically computed spectra. The computed DFT harmonic vibrational force fields (B3LYP and M06 functionals with basis sets of varying flexibility up to 6-311++G**) reproduce well the observed shifts in the IR spectra of both isotopically labeled and structurally related analogues.

  15. Large odd-even staggering in the very light platinum isotopes from laser spectroscopy

    CERN Document Server

    Le Blanc, F; Cabaret, L A; Crawford, J E; Duong, H T; Genevey, J; Girod, M; Huber, G; Krieg, M; Lee, J K P; Lettry, Jacques; Lunney, M D; Obert, J; Oms, J; Peru, S; Putaux, J C; Roussière, B; Sauvage, J; Sebastian, V; Zemlyanoi, S G

    1998-01-01

    Laser spectroscopy measurements have been carried out on very neutron-deficient platinum isotopes with the COMPLIS experimental set-up on line with the ISOLDE-Booster facility. For the first time, Hg alpha -decay was exploited to extend the very light platinum chain. Using the 5d/sup 9/6s /sup 3/D/sub 3/ to 5d/sup 9/6p /sup 3/P /sub 2/ optical transition, hyperfine spectra of /sup 182,181,180,179,178/Pt and /sup 183/Pt/sup m/ were recorded for the first time. The variation of the mean square charge radius between these nuclei, the magnetic moments of the odd isotopes and the quadrupole moment of /sup 183/Pt/sup m/ were thus measured. A large deformation change between /sup 183/Pt/sup 9/ and /sup 183/Pt/sup m/, an odd-even staggering of the charge radius and a deformation drop from A=179 are clearly observed. All these results are discussed and compared with microscopic theoretical predictions using Hartree-Fock- Bogolyubov calculations using the Gogny force. (20 refs).

  16. Light Isotope Abundances in Solar Energetic Particles Measured by the NINA-2 Instrument

    Science.gov (United States)

    Mikhailov, V. V.; Bakaldin, A.; Galper, A.; Koldashov, S.; Korotkov, M.; Leonov, A.; Mikhaylova, J.; Voronov, S.; Bidoli, V.; Casolino, M.; De Pascale, M.; Furano, G.; Iannucci, A.; Morselli, A.; Picozza, P.; Sparvoli, R.; Boezio, M.; Bonvicini, V.; Vacchi, A.; Zampa, N.; Ambriola, M.; Bellotti, R.; Cafagna, F.; Circella, M.; De Marzo, C.; Adriani, O.; Papini, P.; Spillantini, P.; Straulino, S.; Vannuccini, E.; Ricci, M.; Castellini, G.

    2003-07-01

    The instrument NINA-2 flew on board the satellite MITA between July 2000 and August 2001, in circular polar orbit. This paper reports about a set of Solar Energetic Particle events measured by the NINA-2 instrument. The detector has mass resolution of about 0.15 amu for light nuclei and gives the possibility to observe hydrogen and helium isotop es in the energy range 10-50 MeV/n. Data of 3 He and 4 He were used to determine the 3 He/4 He ratio. For each event the deuterium-to-proton ratio was also estimated. This ratio, averaged over all events, is less than 3×10-5 .

  17. Transformation from Ag@Ag3PO4 to Ag@Ag2SO4 hybrid at room temperature: preparation and its visible light photocatalytic activity

    Science.gov (United States)

    Wei, Ting; Gao, Shanmin; Wang, Qingyao; Xu, Hui; Wang, Zeyan; Huang, Baibiao; Dai, Ying

    2017-02-01

    In the present study, Ag/Ag2SO4 hybrid photocatalysts were obtained via a facile redox-precipitation reaction approach by using Ag@Ag3PO4 nanocomposite as the precursor and KMnO4 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 Ag2SO4 can partially transform into metallic Ag during the photocatalytic degradation of organic pollutants, but the Ag/Ag2SO4 hybrids can maintain its structure stability and show enhanced visible light photocatalytic activity because of the surface plasma resonance effect of the metallic Ag.

  18. TiO2分级结构/Ag3 PO4复合材料的可见光催化性能%Photocatalytic Performance of Hierarchical TiO2/Ag3 PO4 Composite Under Visible-light Illumination

    Institute of Scientific and Technical Information of China (English)

    李卫兵; 冯昌; 岳继光; 华方霞; 补钰煜

    2015-01-01

    Urchin-like TiO2 nanomaterial with hierarchical structure(PTHSs) was prepared, then Ag3PO4 nanomaterial with visible-light response was deposited on the hierarchical TiO2 by simple deposition precipitation method, thus a series of PTHSs/Ag3 PO4 composites with efficient visible-light photocatalytic per-formance and stability was synthesized. The photocatalytic performance of the PTHSs/Ag3 PO4 composites for degrading Rhodamine B( RhB) was analyzed. The results show that the photocatalytic performance of PTHSs/Ag3PO4 composite is significantly superior to that of pure Ag3PO4 and that of TiO2(P25)/Ag3PO4 composite. The composite with a PTHSs/Ag3 PO4 molar ratio of 1∶1 showed the best photocatalytic performance and it could decolorize the RhB completely in 6 min under visible light illumination. This is because that the urchin-like TiO2 nanomaterial can provide more load sites than TiO2 nanoparticle for loading Ag3 PO4 . And the hierarchical TiO2 can also improve the contact between the surfaces of TiO2 and Ag3 PO4 so that the separated efficiency of photo-generated electrons-holes by Ag3 PO4 is improved. Meanwhile during the photodegradation process, a little Ag+ on the surface of Ag3 PO4 are gradually reduced to Ag0 , by the plasma resonace effect of which, the absorption and conversion capability of the composite for photon are enhanced and the photocataly-tic performance of the composite material for degrading dyes is further enhanced.%制备了具有分级结构的海胆状TiO2纳米材料,并通过原位沉积法将可见光响应的Ag3 PO4纳米颗粒沉积到TiO2的纳米分级结构上,合成了具有高效稳定可见光催化性能的系列TiO2分级结构/Ag3 PO4复合材料,对比测试了系列材料对罗丹明B( RhB)的光催化降解性能。结果表明, TiO2分级结构/Ag3 PO4复合材料光催化性能明显高于纯相的Ag3 PO4光催化剂,同时也明显优于TiO2( P25)/Ag3 PO4复合光催化剂,其中分级结构TiO2与Ag3 PO4摩尔比为1

  19. Forensic applications of light-element stable isotope ratios of Ricinus communis seeds and ricin preparations.

    Science.gov (United States)

    Kreuzer, Helen W; West, Jason B; Ehleringer, James R

    2013-01-01

    Seeds of the castor plant Ricinus communis are of forensic interest because they are the source of the poison ricin. We tested whether stable isotope ratios of castor seeds and ricin preparations can be used as a forensic signature. We collected over 300 castor seed samples worldwide and measured the C, N, O, and H isotope ratios of the whole seeds and oil. We prepared ricin by three different procedures, acetone extraction, salt precipitation, and affinity chromatography, and compared their isotope ratios to those of the source seeds. The N isotope ratios of the ricin samples and source seeds were virtually identical. Therefore, N isotope ratios can be used to correlate ricin prepared by any of these methods to source seeds. Further, stable isotope ratios distinguished >99% of crude and purified ricin protein samples in pairwise comparison tests. Stable isotope ratios therefore constitute a valuable forensic signature for ricin preparations. © 2012 American Academy of Forensic Sciences.

  20. Light and heavy element isotopic compositions of mainstream SiC grains.

    Energy Technology Data Exchange (ETDEWEB)

    Amari, S.; Clayton, R. N.; Davis, A. M.; Lewis, R. S.; Pellin, M. J.

    1999-02-03

    Although a variety of types of pre-solar SiC grains have been classified by their C, N, and Si isotopic composition, the majority of such grains are so-called mainstream grains and are believed to have come from asymptotic giant branch stars [1]. We have previously reported the Mo isotopic compositions of presolar SiC grains whose C, N, and Si isotopic compositions were not known [2]. Since most presolar SiC grains fall in the mainstream group, we assumed that these grains were mainstream. The excellent match of the Mo isotopic data with expectations for nucleosynthesis in AGB stars was consistent with this identification. In order to better understand the distribution of isotopic compositions in presolar grains, we have begun to measure heavy element isotopic compositions of presolar SiC grains of known C, N and Si isotopic composition.

  1. New yellow-emitting Whitlockite-type structure Sr(1.75)Ca(1.25)(PO4)2:Eu(2+) phosphor for near-UV pumped white light-emitting devices.

    Science.gov (United States)

    Ji, Haipeng; Huang, Zhaohui; Xia, Zhiguo; Molokeev, Maxim S; Atuchin, Victor V; Fang, Minghao; Huang, Saifang

    2014-05-19

    New compound discovery is of interest in the field of inorganic solid-state chemistry. In this work, a whitlockite-type structure Sr1.75Ca1.25(PO4)2 newly found by composition design in the Sr3(PO4)2-Ca3(PO4)2 join was reported. Crystal structure and luminescence properties of Sr1.75Ca1.25(PO4)2:Eu(2+) were investigated, and the yellow-emitting phosphor was further employed in fabricating near-ultraviolet-pumped white light-emitting diodes (w-LEDs). The structure and crystallographic site occupancy of Eu(2+) in the host were identified via X-ray powder diffraction refinement using Rietveld method. The Sr1.75Ca1.25(PO4)2:Eu(2+) phosphors absorb in the UV-vis spectral region of 250-430 nm and exhibit an intense asymmetric broadband emission peaking at 518 nm under λex = 365 nm which is ascribed to the 5d-4f allowed transition of Eu(2+). The luminescence properties and mechanism are also investigated as a function of Eu(2+) concentration. A white LED device which is obtained by combining a 370 nm UV chip with commercial blue phosphor and the present yellow phosphor has been fabricated and exhibit good application properties.

  2. Light-noble-gas isotopic ratios in gases from Mt. Etna (Southern Italy). Implications for mantle contamination and volcanic activity

    Energy Technology Data Exchange (ETDEWEB)

    Italiano, F. [Consiglio Nazionale delle Ricerche, Palermo (Italy). Ist. di Geochimica dei Fluidi; Nuccio, P.M. [Palermo Univ., Palermo (Italy). Ist. di Mineralogia, Petrografia e Geochimica; Nakai, S. [Tokyo Univ., Tokyo (Japan). Lab. for Earthquake Chemistry; Wakita, H. [Tokyo Univ., Tokyo (Japan). Earthquake Research Inst.

    1999-08-01

    Taking into account the light-noble-isotopic ratios signature of gas samples coming from the Etnean area (Southern Italy), it seems that in this area the crustal contamination played a minor role. Instead, processes that enriched the original MORB-type mantle in incompatible elements, have to be considered. The {sup 3}He/{sup 4}He ratios are, thus, lowered because of {sup 1}He produced by radioactive decay of U and Th. On the other hand, helium isotopic ratios have shown wide temporal variations sometimes reaching values as high as 7.6 Ra, out pf typical Etnean range. As these unusually high ratios have been measured during phases of unrest of the volcanic activity at Mt. Etna, this apparent discrepancy in the helium isotopic ratios is considered, as the effect of fractionation processes occurred during the magma uprising.

  3. Electronic isotope shift factors for the Cu $4s \\; ^2S_{1/2} - 4p \\; ^2P^o_{3/2}$ line

    CERN Document Server

    Carette, Thomas

    2016-01-01

    State-of-the-art relativistic multiconfiguration Dirac-Hartree-Fock calculations have been performed to evaluate the electronic field and mass isotope shift factors of the Cu~I resonance line at $\\lambda = 324.8$~nm. A linear correlation between the mass factors and the transition energy is found for elaborate correlation models, allowing extrapolation to the observed frequency limit. The relativistic corrections to the recoil operator reduces the transition mass factor by 5~\\%.

  4. The highly enhanced visible light photocatalytic degradation of gaseous o-dichlorobenzene through fabricating like-flowers BiPO4/BiOBr p-n heterojunction composites

    Science.gov (United States)

    Zou, Xuejun; Dong, Yuying; Zhang, Xiaodong; Cui, Yubo; Ou, Xiaoxia; Qi, Xiaohui

    2017-01-01

    In this paper, in order to enhance photo-induced electron-hole pairs separation of BiOBr, flowers-like BiPO4/BiOBr p-n heterojunction composites was fabricated by a mixing in solvent method. The as-prepared samples were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), high resolution transmission electron microscopy (HRTEM), UV-vis absorption spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), and N2 adsorption-desorption. Meanwhile, their photocatalytic properties were investigated by the degradation of gaseous o-dichlorobenzene under visible light irradiation. Due to its strong adsorption capacity and the formation of p-n heterojunction, compared with BiPO4 and BiOBr, the BiPO4/BiOBr composites showed higher photocatalytic activity in the degradation of gaseous o-DCB under visible light. Among them, 2% BiPO4/BiOBr showed the maximum value of the activity, whose degradation rate was about 2.6 times as great as the pure BiOBr. Furthermore, the OHrad was confirmed the main active species during the photocatalytic process by the trapping experiments. The outstanding performance indicated that the photocatalysts could be applied to air purification for chlorinated volatile organic compound.

  5. Evidence of a circularly polarized light mode along the optic axis in c-cut NH{sub 4}H{sub 2}PO{sub 4}, induced by circular differential reflection and anomalous birefringence

    Energy Technology Data Exchange (ETDEWEB)

    Kaminsky, Werner; Steininger, Steven [Department of Chemistry, University of Washington, Seattle, WA 98195 (United States); Herreros-Cedres, Javier [Departmento de Fisica Basica, Facultad de Fisica, University De La Laguna, La Laguna, Tenerife (Spain); Glazer, Anthony Michael, E-mail: kaminsky@chem.washington.ed [Clarendon Laboratory, University of Oxford, Oxford (United Kingdom)

    2010-03-10

    The anomalous birefringence and circular differential reflection of NH{sub 4}H{sub 2}PO{sub 4} (4-bar2m), cut on the optic axis, have been found to cause an additional signal in measurements of the optical rotation employing polarized light technology, with the sample between crossed and slightly modulated linear polarizers (tilting high accuracy universal polarimetry). The azimuthal rotation of the linearly polarized light, up to 100 times larger than expected, is described in terms of a circularly polarized light mode along the optic axis of varying amplitude. Experimental evidence leading to our conclusion is given and a qualitative model for the effect is presented.

  6. The Preparation of a Highly Efficient Ag3PO4/Ag/Bi2O2CO3 Photo-Catalyst and the Study of Its Photo-Catalytic Organic Synthesis Reaction Driven by Visible Light

    Directory of Open Access Journals (Sweden)

    Zhi Guo

    2017-09-01

    Full Text Available Ag3PO4/Ag/Bi2O2CO3 composites were prepared by a hydrothermal and precipitation method. The morphology, structure, and valence state of the photo-catalysts were characterized by X-ray diffraction (XRD, X-ray photoelectron spectroscopy (XPS, transmission electron microscopy (TEM, Scanning electron microscopy (SEM, Brunauer-Emmett-Teller (BET specific surface areas, and UV-vis diffuse reflectance spectra (UV-vis DRS. They were applied as heterogeneous catalysts in the synthesis of esters from aldehydes (or alcohols and alcohols and the synthesis of imines from alcohols and amines under visible light irradiation. The photo-catalytic activities of the esterification reactions of aldehydes and alcohols were heavily dependent on the loading of Ag3PO4/Ag/Bi2O2CO3 as well as the intensity and wavelength of the visible light. Furthermore, their conversion under visible light irradiation was superior to that in the dark. Herein a reaction mechanism from aldehydes and alcohols to esters was proposed, and the Ag3PO4/Ag/Bi2O2CO3 catalysts could be used six times without a significant decrease in activity. Using these catalysts under visible light could motivate future studies to develop efficient recyclable photo-catalysts and facilitate many synthetic organic reactions.

  7. Light element isotopic compositions of cometary matter returned by the STARDUST mission

    Energy Technology Data Exchange (ETDEWEB)

    McKeegan, K D; Aleon, J; Bradley, J; Brownlee, D; Busemann, H; Butterworth, A; Chaussidon, M; Fallon, S; Floss, C; Gilmour, J; Gounelle, M; Graham, G; Guan, Y; Heck, P R; Hoppe, P; Hutcheon, I D; Huth, J; Ishii, H; Ito, M; Jacobsen, S B; Kearsley, A; Leshin, L A; Liu, M; Lyon, I; Marhas, K; Marty, B; Matrajt, G; Meibom, A; Messenger, S; Mostefaoui, S; Nakamura-Messenger, K; Nittler, L; Palma, R; Pepin, R O; Papanastassiou, D A; Robert, F; Schlutter, D; Snead, C J; Stadermann, F J; Stroud, R; Tsou, P; Westphal, A; Young, E D; Ziegler, K; Zimmermann, L; Zinner, E

    2006-10-10

    Hydrogen, carbon, nitrogen, and oxygen isotopic compositions are heterogeneous among comet 81P/Wild2 particle fragments, however extreme isotopic anomalies are rare, indicating that the comet is not a pristine aggregate of presolar materials. Non-terrestrial nitrogen and neon isotope ratios suggest that indigenous organic matter and highly volatile materials were successfully collected. Except for a single circumstellar stardust grain, silicate and oxide minerals have oxygen isotopic compositions consistent with solar system origin. One refractory grain is {sup 16}O-enriched like refractory inclusions in meteorites, suggesting formation in the hot inner solar nebula and large-scale radial transport prior to comet accretion in the outer solar system.

  8. 水滑石与磷酸银可见光催化剂的活性对比研究%Comparative study of visible-light properties of layered double hydroxides and Ag3PO4 semiconductor photocatalysts

    Institute of Scientific and Technical Information of China (English)

    姜平; 周集体; 张爱丽

    2012-01-01

    本文合成了具备水滑石结构(LDH)的Zn-Cr LDH、Zn-Ti LDH以及Ag3PO43种半导体光催化剂,并对它们的催化性能进行对比研究。XRD和SEM分析表明,Zn-Cr LDH、Zn-Ti LDH具有层状结构而Ag3PO4呈纳米球状结构。UV-Vis分析表明,Ag3PO4和Zn-Cr LDH能够吸收可见光(〉420 nm)。在可见光照射与添加AgNO3作为电子受体的条件下,Zn-TiLDH几乎没有光催化活性,而Ag3PO4的光催化活性高于Zn-Cr LDH。Ag3PO4在光解水实验中180 min内氧气产量约1.2mL,而Zn-Cr LDH约为0.65 mL。光催化降解有机污染物实验中,在Ag3PO4催化作用下,120 min内亚甲基蓝(MB)被完全降解,在240 min内46%的对硝基酚(PNP)被降解,而Zn-Cr LDH相应的去除率分别为61%和27%。%In this study,three semiconductor photocatalysts Ag3PO4,Zn-Cr and Zn-Ti were fabricated and the catalytical performances were investigated.It was showed that Zn-Cr and Zn-Ti possessed the structure of layered double hydroxide(LDH),while Ag3PO4 exhibited nanosphere structure by XRD and SEM analysis.And by UV-vis analysis,Ag3PO4 and Zn-Cr was able to absorb visible light(〉420 nm).However,there is no photocatalytic activity for Zn-Ti when AgNO3 acted as photoelectron acceptor with visible light.Also,it was suggested that Ag3PO4 was more efficient than Zn-Cr.In water splitting experiments,it was produced 1.2 mL and 0.65 mL O2 for Ag3PO4 and Zn-Cr within 180 min,respectively.For organic pollutants degradation,removal rates of methyl blue(MB) by Ag3PO4 and Zn-Cr were nearly 100% and 61%,respectively,within 120 min.Meanwhile,46% and 27% of p-nitrophenol(PNP) could be removed by Ag3PO4 and Zn-Cr,respectively,within 240 min.

  9. Forensic Applications of Light-Element Stable Isotope Ratios of Ricinus communis Seeds and Ricin Preparations

    Energy Technology Data Exchange (ETDEWEB)

    Kreuzer, Helen W.; West, Jason B.; Ehleringer, James

    2013-01-01

    Seeds of the castor plant Ricinus communis, also known as castor beans, are of forensic interest because they are the source of the poison ricin. We have tested whether stable isotope ratios of castor seeds and ricin prepared by various methods can be used as a forensic signature. We collected over 300 castor seed samples from locations around the world and measured the C, N, O, and H stable isotope ratios of the whole seeds, oil, and three types of ricin preparations. Our results demonstrate that N isotope ratios can be used to correlate ricin prepared by any of these methods to source seeds. Further, stable isotope ratios distinguished >99% of crude and purified ricin protein samples in pair-wise comparison tests. Stable isotope ratios therefore constitute a valuable forensic signature for ricin preparations.

  10. Impact of mineral fertility and bedrock erosion on single-mineral detrital studies: insights from trace-element and Nd-isotope systematics of detrital apatite from the Po River catchment

    Science.gov (United States)

    Malusa', Marco Giovanni; Wang, Jiangang; Garzanti, Eduardo; Villa, Igor M.; Wittman, Hella

    2017-04-01

    The detrital record provides an archive of mountain erosion that preserves key information for paleotectonic and paleoclimatic reconstructions. Detrital studies are often based on single-mineral analyses (e.g., geo/thermochronologic analyses on apatite and zircon). Their geologic interpretation can be challenging, because the impact of each eroding source on the detrital record is controlled by a range of factors including the rate of erosion and the fertility of chosen minerals in eroded bedrock. Here, we combine (i) a state-of-the art dataset of trace element and Nd isotope fingerprints of detrital apatite, (ii) a comprehensive dataset of apatite-fertility measurements (Malusà et al. 2016), (iii) fission-track data, and (iv) cosmogenic-derived erosion rates from the Po River catchment (Wittmann et al. 2016), to test the impact of mineral fertility and bedrock erosion on the single-mineral detrital signal preserved in the final sediment sink. Our results show that the information provided by accessory minerals, when complemented with accurate mineral fertility measurements, are fully consistent with information provided by the analysis of more abundant framework minerals. We found that trace element and Nd isotope analyses provide a reliable tool to disentangle the complex single-mineral record of orogenic erosion, and demonstrate that such a record is largely determined by high-fertility source rocks exposed within the drainage. Detrital thermochronology studies based on the lag-time approach should thus preferably include independent provenance discriminations and a full mineral fertility characterization of the potential source areas, in order to ensure a correct identification of the sediment sources and of the exogenic and endogenic processes monitored in the stratigraphic archive. Malusà M.G., Resentini A., Garzanti E., 2016. Hydraulic sorting and mineral fertility bias in detrital geochronology. Gondwana Res., 31, 1-19 Wittmann H., Malusà M.G., Resentini

  11. A novel P/Ag/Ag2O/Ag3PO4/TiO2 composite film for water purification and antibacterial application under solar light irradiation.

    Science.gov (United States)

    Zhu, Qi; Hu, Xiaohong; Stanislaus, Mishma S; Zhang, Nan; Xiao, Ruida; Liu, Na; Yang, Yingnan

    2017-01-15

    TiO2-based thin films have been intensively studied in recent years to develop efficient photocatalyst films to degrade refractory organics and inactivate bacteria for wastewater treatment. In the present work, P/Ag/Ag2O/Ag3PO4/TiO2 composite films on the inner-surface of glass tube were successfully prepared via sol-gel approach. P/Ag/Ag2O/Ag3PO4/TiO2 composite films with 3 coating layers, synthesized at 400°C for 2h, showed the optimal photocatalytic performance for rhodamine B (Rh B) degradation. The results indicated that degradation ratio of Rh B by P/Ag/Ag2O/Ag3PO4/TiO2 composite film reached 99.9% after 60min under simulated solar light, while just 67.9% of Rh B was degraded by pure TiO2 film. Moreover, repeatability experiments indicated that even after five recycling runs, the photodegradation ratio of Rh B over composite film maintained at 99.9%, demonstrating its high stability. Photocatalytic inactivation of E. coli with initial concentration of 10(7)CFU/mL also showed around 100% of sterilization ratio under simulated solar light irradiation in 5min by the composite film. The radical trapping experiments implied that the major active species of P/Ag/Ag2O/Ag3PO4/TiO2 composite films were photo-generated holes and O2(-) radicals. The proposed photocatalytic mechanism shows that the transfer of photo-induced electrons and holes may reduce the recombination efficiency of electron-hole pairs and potential photodecomposition of composite film, resulting in enhanced photocatalytic ability of P/Ag/Ag2O/Ag3PO4/TiO2 composite films.

  12. NMR investigation on isotope effect of glycinium phosphite H sub 3 NCH sub 2 COOH centre dot H sub 2 PO sub 3

    CERN Document Server

    Ishibashi, T

    2003-01-01

    The motions of the phosphite anions and glycinium cations in H sub 3 NCH sub 2 COOH centre dot H sub 2 PO sub 3 (GPI) and its deuterated analogue (DGPI) were investigated by sup 1 H, sup 1 sup 3 C and sup 3 sup 1 P spin-lattice relaxation times T sub 1. For both GPI and DGPI, T sub 1 's of the sup 1 H, sup 1 sup 3 C and sup 3 sup 1 P nuclei reflect the amino rotation, methylene libration and motion of the phosphite anions, respectively. Activation energies obtained from T sub 1 's of sup 1 H, sup 1 sup 3 C and sup 3 sup 1 P nuclei are 28.6(2), 26.0(4) and 26.2(4) kJ/mol for GPI and are 34.9(6), 27(1), 47(2) kJ/mol for DGPI, respectively. The deuterium substitution increases E sub a for the motion influenced by the hydrogen bonding. In all the observed motions, correlation times of DGPI are larger than those of GPI. (author)

  13. Determination of carbon isotopic composition of individual light hydrocarbons evolved from pyrolysis of source rocks by using GC-IRMS

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    The carbon isotopic composition of individual light hydrocarbons generated from source rocks that had been pyrolysed in vacuum glass tube were determined by using the GC-IRMS techniques. The results indicate that abundant CO2 in the pyrolysates has a remarkable effect on the determination of CH4δ13C. Running cryogenically with an initial temperature of -40℃can effectively eliminate the effect. In addition, it conduces to measuring the δ13C of C2+ hydrocarbons by increasing the injection volume and/or absorbing CO2 with the solution of sodium hydroxide.The above measures will help to get the carbon isotopic composition of C1-C7 components, which is of great significance for gas/source rock correlation and for study on the genesis of natural gas.

  14. Distribution of light element isotopes in Bencubbin and Weatherford meteorites: An indicator of heterogeneity in the primitive solar nebula

    Energy Technology Data Exchange (ETDEWEB)

    Blacic, J.; Maggiore, C.; Taylor, J.; Newsom, H.; Marti, K.

    1994-09-01

    The objective is to study light element isotopes, particularly {sup 15}N, in meteorites to elucidate early solar nebula processes. The approach is to use microion beams to induce characteristic nuclear reactions in specific minerals in the meteorites, and to develop isotope imaging techniques by beam rastering. Early results demonstrate the feasibility of the beam rastering technique and we have successfully measured a {delta}{sup 15}N ratio of about -50 {per_thousand} in sinoite (Si{sub 2}N{sub 2}O) in an enstatite chondrite. No conclusions can be drawn at this stage of the investigation. Ultimately, the results are important to understanding conditions during planetary formation, and in developing new analytic techniques applicable to a wide range of geophysical problems.

  15. Cold and warm white light generation using Zn(PO{sub 3}){sub 2} glasses activated by Ce{sup 3+}, Dy{sup 3+} and Mn{sup 2+}

    Energy Technology Data Exchange (ETDEWEB)

    Caldino, U., E-mail: cald@xanum.uam.mx [Departamento de Fisica, Universidad Autonoma Metropolitana-Iztapalapa, P.O. Box 55-534, 09340 Mexico, D.F. (Mexico); Alvarez, E. [Departamento de Fisica, Universidad de Sonora (UNISON), Boulevard Luis Encinas y Rosales s/n, Hermosillo, Sonora 83000 (Mexico); Speghini, A.; Bettinelli, M. [Dipartimento di Biotecnologie, Universita di Verona, and INSTM, UdR Verona, Strada Le Grazie 15, I-37314 Verona (Italy)

    2012-08-15

    The photoluminescence of zinc metaphosphate glasses activated by Dy{sup 3+}, Ce{sup 3+}/Dy{sup 3+} and Ce{sup 3+}/Dy{sup 3+}/Mn{sup 2+} ions was investigated. Non-radiative energy transfers from Ce{sup 3+} to Dy{sup 3+} and Ce{sup 3+} to Mn{sup 2+} are observed upon 280 nm excitation. The non-radiative nature of these transfers is inferred from the increase in the decay rate of the Ce{sup 3+} emission when the glass is co-doped with Dy{sup 3+} or Dy{sup 3+}/Mn{sup 2+}. It is demonstrated that zinc metaphosphate glasses can generate cold or warm white light emission when they are doped with Ce{sup 3+}/Dy{sup 3+} or Ce{sup 3+}/Dy{sup 3+}/Mn{sup 2+} and pumped at 280 nm (peak emission wavelength of AlGaN-based LEDs). The CIE1931 chromaticity coordinates and color temperature were (0.34, 0.35) and 5250 K for the cold light, and (0.47, 0.43) and 2700 K for the warm light. - Highlights: Black-Right-Pointing-Pointer Non-radiative energy transfer from Ce{sup 3+} to Dy{sup 3+} and Mn{sup 2+} takes place in Zn(PO{sub 3}){sub 2} glasses doped with Ce{sup 3+}/Dy{sup 3+}/Mn{sup 2+}. Black-Right-Pointing-Pointer Zn(PO{sub 3}){sub 2} glasses doped with Ce{sup 3+}/Dy{sup 3+} can generate 5250 K cold white light emission. Black-Right-Pointing-Pointer Zn(PO{sub 3}){sub 2} glasses doped with Ce{sup 3+}/Dy{sup 3+}/Mn{sup 2+} can generate 2700 K warm yellowish orange light emission.

  16. Synthesis and characterization of Ag{sub 3}PO{sub 4} immobilized with graphene oxide (GO) for enhanced photocatalytic activity and stability over 2,4-dichlorophenol under visible light irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Xiao-juan [Department of Environmental Science and Engineering, Xiangtan University, Xiangtan 411105 (China); Dai, You-zhi, E-mail: daiyzh@xtu.edu.cn [Department of Environmental Science and Engineering, Xiangtan University, Xiangtan 411105 (China); Wang, Xing-yan; Guo, Jing; Liu, Tan-hua [Department of Environmental Science and Engineering, Xiangtan University, Xiangtan 411105 (China); Li, Fen-fang [Department of Environmental Science and Engineering, Xiangtan University, Xiangtan 411105 (China); Department of Environmental Science, Changsha Environmental Protection Vocational College, Changsha410004 (China)

    2015-07-15

    Highlights: • A series of Ag{sub 3}PO{sub 4}–GO photocatalysts with different GO content were prepared. • Photocatalytic activity of Ag{sub 3}PO{sub 4}–GO to 2,4-DCP increased with GO content increasing. • GO played significant role in the enhanced photocatalytic activity and stability. • Degradation pathway of 2,4-DCP and photocatalytic mechanism of Ag{sub 3}PO{sub 4}–GO were proposed. - Abstract: A series of visible-light responsive photocatalysts prepared using Ag{sub 3}PO{sub 4} immobilized with graphene oxide (GO) with varying GO content were obtained by an electrostatically driven method, and 2,4-dichlorophenol (2,4-DCP) was used to evaluate the performance of the photocatalysts. The composites exhibited superior photocatalytic activity and stability compared with pure Ag{sub 3}PO{sub 4}. When the content of GO was 5%, the degradation efficiency of 2,4-DCP could reach 98.95%, and 55.91% of the total organic (TOC) content was removed within 60 min irradiation. Meanwhile, the efficiency of 91.77% was achieved for 2,4-DCP degradation even after four times of recycling in the photocatalysis/Ag{sub 3}PO{sub 4}–GO (5%) system. Reactive species of O{sub 2}{sup ·−}, OH· and h{sup +} were considered as the main participants for oxidizing 2,4-DCP, as confirmed by the free radical capture experiments. And some organic intermediates including 4-chlorophenol (4-CP), hydroquinone (HQ), benzoquinone (BZQ), 2-chlorohydroquinone and hydroxyhydroquinone (HHQ) were detected by comparison with the standard retention times from the high performance liquid chromatography (HPLC). In short, the enhanced photocatalytic property of Ag{sub 3}PO{sub 4}–GO was closely related to the strong absorption ability of GO relative to 2,4-DCP, the effective separation of photogenerated electron–hole pairs, and the excellent electron capture capability of GO.

  17. The isotopic composition of valves and organic tissue of diatoms grown in steady state cultures under varying conditions of temperature, light and nutrients. Implications for the interpretation of oxygen isotopes from sedimentary biogenic opal as proxies of environmental variations

    Energy Technology Data Exchange (ETDEWEB)

    Kowalczyk, K.

    2006-05-15

    The oxygen isotopes of diatomaceous silica from marine and freshwater sediments are frequently used as indicators of the palaeotemperature development, particularly in cases where calcareous microfossils are rare or absent. With regard to terrestrial waters it is unknown whether or not palaeotemperature scale can be used in a limnic ecosystem. Due to the fact that the seasonal variations in lakes are larger than in oceans, specific problems arise when working with freshwater sediments. Thus, an understanding of the contribution of the various factors (e.g. temperature, light nutrients, competition) influencing the formation of isotope signals in biogenic opal is a prerequisite for the accurate interpretation of environmental processes. Since it is impossible to examine the influence of a single parameter under natural ecosystem conditions due to permanent changes of the environment, laboratory experiments with single diatom species are needed. Therefore, the aim of this study was to investigate the correlation between the oxygen isotope variations in biogenic opal and different environmental parameters using steady state cultures with diatoms. It should be examined whether or not the different diatom species grown under identical conditions show equal oxygen isotope ratios (species relationship), if variations of the water temperature induce variations of the oxygen isotope ratio (relationship with temperature), variable parameters such as light intensity and nitrate concentration influence the isotope ratio, and if vital effects (e.g. growth rate) lead to variations of the oxygen isotope ratio. (orig.)

  18. Improvement of water and light availability after thinning at a xeric site: which matters more? A dual isotope approach.

    Science.gov (United States)

    Giuggiola, Arnaud; Ogée, Jérôme; Rigling, Andreas; Gessler, Arthur; Bugmann, Harald; Treydte, Kerstin

    2016-04-01

    Thinning fosters individual tree growth by increasing the availability of water, light and nutrients. At sites where water rather than light is limiting, thinning also enhances soil evaporation and might not be beneficial. Detailed knowledge of the short- to long-term physiological response underlying the growth responses to thinning is crucial for the management of forests already suffering from recurrent drought-induced dieback. We applied a dual isotope approach together with mechanistic isotope models to study the physiological processes underlying long-term growth enhancement of heavily thinned Pinus sylvestris in a xeric forest in Switzerland. This approach allowed us to identify and disentangle thinning-induced changes in stomatal conductance and assimilation rate. At our xeric study site, the increase in stomatal conductance far outweighed the increase in assimilation, implying that growth release in heavily thinned trees is primarily driven by enhanced water availability rather than increased light availability. We conclude that in forests with relatively isohydric species (drought avoiders) that are growing close to their physiological limits, thinning is recommended to maintain a less negative water balance and thus foster tree growth, and ultimately the survival of forest trees under drought. © 2015 The Authors. New Phytologist © 2015 New Phytologist Trust.

  19. Light stable isotope study of the Roosevelt Hot Springs thermal area, Southwestern Utah

    Energy Technology Data Exchange (ETDEWEB)

    Rohrs D.T.; Bowman, J.R.

    1980-05-01

    The isotopic composition of hydrogen, oxygen, and carbon has been determined for regional cold springs, thermal fluids, and rocks and minerals from the Roosevelt Hot Springs thermal area. The geothermal system has developed within plutonic granitic rocks and amphibolite facies gneiss, relying upon fracture-controlled permeability for the migration of the thermal fluids. Probably originating as meteoric waters in the upper elevations of the Mineral Mountains, the thermal waters sampled in the production wells display an oxygen isotopic shift of at least +1.2. Depletions of delta /sup 18/O in wole rock, K-feldspar, and biotite have a positive correlation with alteration intensity. W/R mass ratios, calculated from the isotopic shifts of rock and water, range up to 3.0 in a producing horizon of one well, although the K-feldspar has experienced only 30% exchange with the thermal waters. While veinlet quartz has equilibrated with the thermal waters, the /sup 18/O values of K-mica clay, an alteration product of plagioclase, mimic the isotopic composition of K-feldspar and whole rock. This suggests that locally small W/R ratios enable plagioclase to influence its alteration products by isotopic exchange.

  20. Isotopic Composition of Light Nuclei in Cosmic Rays: Results from AMS-01

    Science.gov (United States)

    Aguilar, M.; Alcaraz, J.; Allaby, J.; Alpat, B.; Ambrosi, G.; Anderhub, H.; Ao, L.; Arefiev, A.; Arruda, L.; Azzarello, P.; Basile, M.; Barao, F.; Barreira, G.; Bartoloni, A.; Battiston, R.; Becker, R.; Becker, U.; Bellagamba, L.; Berdugo, J.; Berges, P.; Bertucci, B.; Biland, A.; Bindi, V.; Boella, G.; Boschini, M.; Bourquin, M.; Bruni, G.; Buénerd, M.; Burger, J. D.; Burger, W. J.; Cai, X. D.; Cannarsa, P.; Capell, M.; Casadei, D.; Casaus, J.; Castellini, G.; Cernuda, I.; Chang, Y. H.; Chen, H. F.; Chen, H. S.; Chen, Z. G.; Chernoplekov, N. A.; Chiueh, T. H.; Choi, Y. Y.; Cindolo, F.; Commichau, V.; Contin, A.; Cortina-Gil, E.; Crespo, D.; Cristinziani, M.; Dai, T. S.; dela Guia, C.; Delgado, C.; Di Falco, S.; Djambazov, L.; D'Antone, I.; Dong, Z. R.; Duranti, M.; Engelberg, J.; Eppling, F. J.; Eronen, T.; Extermann, P.; Favier, J.; Fiandrini, E.; Fisher, P. H.; Flügge, G.; Fouque, N.; Galaktionov, Y.; Gervasi, M.; Giovacchini, F.; Giusti, P.; Grandi, D.; Grimm, O.; Gu, W. Q.; Haino, S.; Hangarter, K.; Hasan, A.; Hermel, V.; Hofer, H.; Hungerford, W.; Ionica, M.; Jongmanns, M.; Karlamaa, K.; Karpinski, W.; Kenney, G.; Kim, D. H.; Kim, G. N.; Kim, K. S.; Kirn, T.; Klimentov, A.; Kossakowski, R.; Kounine, A.; Koutsenko, V.; Kraeber, M.; Laborie, G.; Laitinen, T.; Lamanna, G.; Laurenti, G.; Lebedev, A.; Lechanoine-Leluc, C.; Lee, M. W.; Lee, S. C.; Levi, G.; Lin, C. H.; Liu, H. T.; Lu, G.; Lu, Y. S.; Lübelsmeyer, K.; Luckey, D.; Lustermann, W.; Maña, C.; Margotti, A.; Mayet, F.; McNeil, R. R.; Menichelli, M.; Mihul, A.; Mujunen, A.; Natale, S.; Oliva, A.; Palmonari, F.; Paniccia, M.; Park, H. B.; Park, W. H.; Pauluzzi, M.; Pauss, F.; Pereira, R.; Perrin, E.; Pevsner, A.; Pilo, F.; Pimenta, M.; Plyaskin, V.; Pojidaev, V.; Pohl, M.; Produit, N.; Quadrani, L.; Rancoita, P. G.; Rapin, D.; Ren, D.; Ren, Z.; Ribordy, M.; Riihonen, E.; Ritakari, J.; Ro, S.; Roeser, U.; Sagdeev, R.; Santos, D.; Sartorelli, G.; Saouter, P.; Sbarra, C.; Schael, S.; Schultz von Dratzig, A.; Schwering, G.; Seo, E. S.; Shin, J. W.; Shoumilov, E.; Shoutko, V.; Siedenburg, T.; Siedling, R.; Son, D.; Song, T.; Spada, F. R.; Spinella, F.; Steuer, M.; Sun, G. S.; Suter, H.; Tang, X. W.; Ting, Samuel C. C.; Ting, S. M.; Tomassetti, N.; Tornikoski, M.; Torsti, J.; Trümper, J.; Ulbricht, J.; Urpo, S.; Valtonen, E.; Vandenhirtz, J.; Velikhov, E.; Verlaat, B.; Vetlitsky, I.; Vezzu, F.; Vialle, J. P.; Viertel, G.; Vité, D.; Von Gunten, H.; Waldmeier Wicki, S.; Wallraff, W.; Wang, J. Z.; Wiik, K.; Williams, C.; Wu, S. X.; Xia, P. C.; Xu, S.; Xu, Z. Z.; Yan, J. L.; Yan, L. G.; Yang, C. G.; Yang, J.; Yang, M.; Ye, S. W.; Zhang, H. Y.; Zhang, Z. P.; Zhao, D. X.; Zhou, F.; Zhou, Y.; Zhu, G. Y.; Zhu, W. Z.; Zhuang, H. L.; Zichichi, A.; Zimmermann, B.; Zuccon, P.

    2011-08-01

    The variety of isotopes in cosmic rays allows us to study different aspects of the processes that cosmic rays undergo between the time they are produced and the time of their arrival in the heliosphere. In this paper, we present measurements of the isotopic ratios 2H/4He, 3He/4He, 6Li/7Li, 7Be/(9Be+10Be), and 10B/11B in the range 0.2-1.4 GeV of kinetic energy per nucleon. The measurements are based on the data collected by the Alpha Magnetic Spectrometer, AMS-01, during the STS-91 flight in 1998 June.

  1. Isotopic Composition of Light Nuclei in Cosmic Rays: Results from AMS-01

    CERN Document Server

    Aguilar, M; Wiik, K; Grimm, O; Sartorelli, G; Zhou, Y; Pauss, F; Alpat, B; Capell, M; Djambazov, L; Yang, M; Yang, J; Extermann, P; Arefiev, A; Zhuang, H L; Hermel, V; Mihul, A; Galaktionov, Y; Park, H B; Von Gunten, H; Vetlitsky, I; Zhou, F; Vandenhirtz, J; Ambrosi, G; Suter, H; Becker, U; Zhang, H Y; Alcaraz, J; Casaus, J; Ren, Z; Fiandrini, E; Hungerford, W; Ren, D; Wicki, S W; Eppling, F J; Flugge, G; Karlamaa, K; Boella, G; Levi, G; Choi, Y Y; Laborie, G; Lubelsmeyer, K; Gervasi, M; Kirn, T; Azzarello, P; Kounine, A; Barreira, G; Yan, L G; Burger, W J; Koutsenko, V; Grandi, D; Ribordy, M; Gu, W Q; Bindi, V; Favier, J; Haino, S; Shin, J W; Mana, C; Seo, E S; Plyaskin, V; Shoumilov, E; Cannarsa, P; Xia, P C; Ionica, M; Jongmanns, M; Shoutko, V; Wallraff, W; Margotti, A; Lee, S C; Giovacchini, F; Schael, S; Bourquin, M; Roeser, U; Lu, Y S; Torsti, J; Kossakowski, R; Chang, Y H; Menichelli, M; Verlaat, B; Paniccia, M; Steuer, M; Fouque, N; Boschini, M; Zimmermann, B; Song, T; Zuccon, P; Contin, A; Produit, N; Laitinen, T; Kim, K S; Viertel, G; Lin, C H; Lechanoine-Leluc, C; Delgado, C; Lu, G; Pohl, M; Yang, C G; Tornikoski, M; Duranti, M; Cindolo, F; Xu, S; Lebedev, A; Xu, Z Z; Crespo, D; Cristinziani, M; Tomassetti, N; Kim, D H; Biland, A; Bertucci, B; Trumper, J; Buenerd, M; Hangarter, K; Kenney, G; Quadrani, L; Hofer, H; Berdugo, J; Siedenburg, T; Chen, Z G; Ting, S M; Vezzu, F; Cortina-Gil, E; Dai, T S; Barao, F; Commichau, V; Zhang, Z P; Sun, G S; Zhu, W Z; Laurenti, G; Chen, H S; Kim, G N; Sagdeev, R; Wu, S X; Urpo, S; Lee, M W; Rapin, D; Kraeber, M; Chen, H F; Engelberg, J; Ritakari, J; Di Falco, S; Zhu, G Y; Vite, D; Ulbricht, J; Bruni, G; Bellagamba, L; Williams, C; Fisher, P H; D'Antone, I; Pevsner, A; Castellini, G; Chernoplekov, N A; Ao, L; Giusti, P; McNeil, R R; Allaby, J; Yan, J L; Son, D; Santos, D; Cai, X D; Rancoita, P G; Becker, R; Wang, J Z; Oliva, A; Karpinski, W; Cernuda, I; Saouter, P; Ro, S; Anderhub, H; Dela Guia, C; Schwering, G; Ting, S C C; Lamanna, G; Pauluzzi, M; Berges, P; Riihonen, E; Pojidaev, V; Chiueh, T H; Valtonen, E; Pereira, R; Spinella, F; Perrin, E; Park, W H; Dong, Z R; Zichichi, A; Battiston, R; von Dratzig, A S; Vialle, J P; Klimentov, A; Liu, H T; Bartoloni, A; Arruda, L; Tang, X W; Mujunen, A; Pimenta, M; Casadei, D; Spada, F R; Eronen, T; Mayet, F; Palmonari, F; Lustermann, W; Velikhov, E; Pilo, F; Zhao, D X; Luckey, D; Basile, M; Sbarra, C; Natale, S; Siedling, R; Ye, S W; Burger, J D

    2011-01-01

    The variety of isotopes in cosmic rays allows us to study different aspects of the processes that cosmic rays undergo between the time they are produced and the time of their arrival in the heliosphere. In this paper, we present measurements of the isotopic ratios (2)H/(4)He, (3)He/(4)He, (6)Li/(7)Li, (7)Be/((9)Be+(10)Be), and (10)B/(11)B in the range 0.2-1.4 GeV of kinetic energy per nucleon. The measurements are based on the data collected by the Alpha Magnetic Spectrometer, AMS-01, during the STS-91 flight in 1998 June.

  2. Isotopic Composition of Light Nuclei in Cosmic Rays: Results from AMS-01

    OpenAIRE

    Aguilar, M.; Alcaraz, J.; Allaby, J.; Alpat, B.; Ambrosi, G.; Anderhub, H.; Ao, L.; Arefiev, A.; Arruda, L.; P. Azzarello(c); Basile, M.; Barao, F.; G. Barreira(LIP Lisboa); Bartoloni, A; Battiston, R.

    2011-01-01

    The variety of isotopes in cosmic rays allows us to study different aspects of the processes that cosmic rays undergo between the time they are produced and the time of their arrival in the heliosphere. In this paper, we present measurements of the isotopic ratios 2H/4He, 3He/4He, 6Li/7Li, 7Be/(9Be+10Be), and 10B/11B in the range 0.2–1.4 GeV of kinetic energy per nucleon. The measurements are based on the data collected by the Alpha Magnetic Spectrometer, AMS-01, during the STS-91...

  3. Variation in oxygen isotope ratio of dissolved orthophosphate induced by uptake process in natural coral holobionts

    Science.gov (United States)

    Ferrera, Charissa M.; Miyajima, Toshihiro; Watanabe, Atsushi; Umezawa, Yu; Morimoto, Naoko; San Diego-McGlone, Maria Lourdes; Nadaoka, Kazuo

    2016-06-01

    A model incubation experiment using natural zooxanthellate corals was conducted to evaluate the influence of phosphate uptake by coral holobionts on oxygen isotope ratio of dissolved PO4 3- (δ18Op). Live coral samples of Acropora digitifera, Porites cylindrica, and Heliopora coerulea were collected from coral reefs around Ishigaki Island (Okinawa, Japan) and Bolinao (northern Luzon, Philippines) and incubated for 3-5 d after acclimatization under natural light conditions with elevated concentrations of PO4 3-. Phosphate uptake by corals behaved linearly with incubation time, with uptake rate depending on temperature. δ18Op usually increased with time toward the equilibrium value with respect to oxygen isotope exchange with ambient seawater, but sometimes became higher than equilibrium value at the end of incubation. The magnitude of the isotope effect associated with uptake depended on coral species; the greatest effect was in A. digitifera and the smallest in H. coerulea. However, it varied even within samples of a single coral species, which suggests multiple uptake processes with different isotope effects operating simultaneously with varying relative contributions in the coral holobionts used. In natural environments where concentrations of PO4 3- are much lower than those used during incubation, PO4 3- is presumably turned over much faster and the δ18Op easily altered by corals and other major primary producers. This should be taken into consideration when using δ18Op as an indicator of external PO4 3- sources in coastal ecosystems.

  4. Synthesis, luminescent properties and white light emitting diode application of Ba7Zr(PO4)6:Eu2+ yellow-emitting phosphor

    Science.gov (United States)

    Li, Chenxia; Dai, Jian; Deng, Degang; Shen, Changyu; Xu, Shiqing

    2015-10-01

    A yellow-emitting phosphor, Eu2+-activated Ba7Zr(PO4)6 phosphor was synthesized by solid-state reaction method and the luminescence properties were investigated. The phosphor exhibited strong absorption in near ultraviolet (n-UV) region, which matched well with the n-UV chip. Upon excitation at 370 nm, the Ba7Zr(PO4)6:Eu2+ phosphor has a broad yellow emission band with a peak at 585 nm and a full width at half maximum of 178 nm wider than that of the commercial yellow-emitting YAG:Ce3+ phosphor. The mechanism of concentration quenching of Eu2+ ions in Ba7Zr(PO4)6 phosphor is verified to be energy transfer among the nearest neighbor Eu2+ ions. The CIE value and temperature dependence of photoluminescence were also discussed. Furthermore, a white-LED was fabricated using a 370 nm UV chip pumped with a blend of phosphors consisting of yellow-emitting Ba6.97Zr(PO4)6:0.03Eu2+ and blue-emitting BaMgAl10O17:Eu2+ phosphors, which achieved a CIE of (0.3329, 0.3562) with a color-rendering index of 86.4 around the CCT of 5487 K.

  5. BiPO4 photocatalyst employing synergistic action of Ag/Ag3PO4 nanostructure and graphene nanosheets

    Science.gov (United States)

    Mohaghegh, N.; Rahimi, E.

    2016-06-01

    Graphene-supported BiPO4/Ag/Ag3PO4 photocatalyst has been fabricated by simple hydrothermal and impregnation reaction. In BiPO4/Ag/Ag3PO4 based on Reduced Graphene Oxide (RGO), this network renders numerous pathways for rapid mass transport, strong adsorption and multireflection of incident light; meanwhile, the interface between BiPO4/Ag/Ag3PO4 and RGO increases the active sites and electron transfer rate. BiPO4/Ag/Ag3PO4 based on RGO noticeably exhibited high photocatalytic activity than that of BiPO4/Ag/Ag3PO4 and P25 under visible light irradiation for cationic dye (Rhodamine B), anionic dye (methyl orange) and 4-chlorophenol (4-CP) as a neutral pollutant, which are usually difficult to be degraded over the other catalysts. This enhanced photocatalytic activity of Graphene-supported BiPO4/Ag/Ag3PO4 for all pollutants could be mainly ascribed to the reinforced charge transfer from BiPO4/Ag/Ag3PO4 to RGO, which suppresses the recombination of electron/hole pairs. Besides that, this photocatalyst can be used repetitively with a high photocatalytic activity and no apparent loss of activity occurs. The results reveal that the RGO nanosheets work as a photocatalyst promoter during the photocatalytic reaction, leading to an improved photocatalytic activity.

  6. Water and light improvement after thinning at a xeric site: Which weights the most? A dual isotope approach

    Science.gov (United States)

    Giuggiola, Arnaud; Ogée, Jérôme; Gessler, Arthur; Rigling, Andreas; Bugmann, Harald; Treydte, Kerstin

    2015-04-01

    Reductions in stand density foster individual tree growth due to increases of resources such as water, light and nutrients. Detailed knowledge of the short- to long-term physiological response underlying the growth response to thinning is crucial for the management of forests already suffering from recurrent drought-induced dieback. We applied a dual isotope approach together with mechanistic isotope models such as MuSICA to study the physiological processes underlying growth enhancement in a long-term thinning experiment in a xeric Pinus sylvestris forest in Switzerland. This approach allowed for identifying and disentangling changes in stomatal conductance and assimilation rate. Our results indicate that an increase in stomatal conductance outweighs an increase in assimilation, meaning that the observed growth releases in heavy thinned trees at our xeric site are primarily driven by enhanced water availability rather than by the increase in light availability. We conclude that in areas with isohydric species (drought avoiders) that tend to grow close to their physiological limits, thinning is highly recommended to maintain a less negative water balance and thus foster tree growth, and ultimately the survival rate of individual trees and forests.

  7. Sonophotocatalytic degradation of trypan blue and vesuvine dyes in the presence of blue light active photocatalyst of Ag3PO4/Bi2S3-HKUST-1-MOF: Central composite optimization and synergistic effect study.

    Science.gov (United States)

    Mosleh, S; Rahimi, M R; Ghaedi, M; Dashtian, K

    2016-09-01

    An efficient simultaneous sonophotocatalytic degradation of trypan blue (TB) and vesuvine (VS) using Ag3PO4/Bi2S3-HKUST-1-MOF as a novel visible light active photocatalyst was carried out successfully in a continuous flow-loop reactor equipped to blue LED light. Ag3PO4/Bi2S3-HKUST-1-MOF with activation ability under blue light illumination was synthesized and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray (EDX), photoluminescence (PL) and diffuse reflectance spectra (DRS). The effect of operational parameters such as the initial TB and VS concentration (5-45mg/L), flow rate (30-110mL/min), irradiation and sonication time (10-30min), pH (3-11) and photocatalyst dosage (0.15-0.35g/L) has been investigated and optimized using central composite design (CCD) combined with desirability function (DF). Maximum sonophotodegradation percentage (98.44% and 99.36% for TB and VS, respectively) was found at optimum condition set as: 25mg/L of each dye, 70mL/min of solution flow rate, 25min of irradiation and sonication time, pH 6 and 0.25g/L of photocatalyst dosage. At optimum conditions, synergistic index value was obtained 2.53 that indicated the hybrid systems including ultrasound irradiation and photocatalysis have higher efficiency compared with sum of the individual processes.

  8. Comparison of Self-Consistent Skyrme and Gogny Calculations for Light Hg Isotopes

    CERN Document Server

    Warda, M; Próchniak, L

    2009-01-01

    The ground-state properties of neutron-deficient Hg isotopes have been investigated by the constrained self-consistent Hartree-Fock-Bogoliubov approach with the Skyrme and Gogny effective forces. In the case of the Skyrme interaction we h ave also applied the Hartree-Fock+BCS model with the state-dependent $\\delta$-pairing interaction. Potential energy surfaces and pairing properties have been compared for the both types of forces.

  9. Discrimination between ginseng from Korea and China by light stable isotope analysis

    Energy Technology Data Exchange (ETDEWEB)

    Horacek, Micha, E-mail: micha.horacek@ait.ac.at [Department of Environmental Resources and Technology, Austrian Institute of Technology, 2444 Seibersdorf (Austria); Min, Ji-Sook; Heo, Sang-Cheol [National Institute of Scientific Investigation, 331-1 Shinwol-7dong, Yangcheon-ku, Seoul 158-707 (Korea, Republic of); Soja, Gerhard [Department of Environmental Resources and Technology, Austrian Institute of Technology, 2444 Seibersdorf (Austria)

    2010-12-03

    Ginseng is a health food and traditional medicine highly valued in Asia. Ginseng from certain origins is higher valued than from other origins, so that a reliable method for differentiation of geographical origin is important for the economics of ginseng production. To discriminate between ginseng samples from South Korea and PR China, 29 samples have been analyzed for the isotopic composition of the elements H, C and N. The results showed {delta}{sup 2}H values between -94 and -79 per mille , for {delta}{sup 13}C -27.9 to -23.7 per mille and for {delta}{sup 15}N 1.3-5.4 per mille for Chinese ginseng. Korean ginseng gave {delta}{sup 2}H ratios between -91 and -69 per mille , {delta}{sup 13}C ratios between -31.2 and -22.4 per mille and {delta}{sup 15}N ratios between -2.4 and +7 per mille . Despite the overlap between the values for individual isotopes, a combination of the isotope systems gave a reasonable differentiation between the two geographic origins. Especially the statistically significant difference in {delta}{sup 2}H ratios facilitated the differentiation between Korean and Chinese ginseng samples.

  10. Synthesis of TiO2@Ag3 PO4 photocatalyst and its performance for degradation of Safranine T under ultraviolet-light irridiation%TiO2@Ag3 PO4光催化剂的制备及其紫外光催化降解番红花红T反应性能

    Institute of Scientific and Technical Information of China (English)

    李大军; 贺惠

    2015-01-01

    采用化学沉淀法(两步法)制备了TiO2@Ag3 PO4复合光催化剂,考察了该光催化剂在紫外光(λ=254 nm)下对阳离子染料废水中番红花红T降解的催化性能,探讨了催化剂的投加量、番红花红T废水初始浓度、反应温度、避光吸附催化反应以及循环使用对TiO2@Ag3 PO4催化性能的影响。结果表明,当TiO2@Ag3 PO4催化剂投加量为0.7 g/L,番红花红T染料废水的初始浓度为70 mg/L,紫外光照35 min,反应温度为20℃(室温)时,达到最佳降解条件,其催化降解率高达97.9%,并且催化剂循环使用5次后,催化活性无明显下降。在避光黑暗条件下,催化剂对番红花红T 40 min最大吸附量仅为2.3 mg/g;反应体系温度与催化剂的催化性能呈明显负相关,高温催化会降低其催化性能,说明该催化剂的高温稳定性还有待于进一步提高。%The chemical precipitation method ( two-step method) were applied to make TiO2@Ag3 PO4 ,a composite photocatalyst. The degradation catalytic effects of TiO2@Ag3 PO4 under UV light (λ=254 nm) on Safranine T in cationic dye wastewater was explored and the input amount of the catalyst,Safranine T wastewater’ s initial concentration,reaction temperature,photophobic adsorption catalytic reaction and the effect of circular use on the catalytic performance of TiO2@Ag3 PO4 are further discussed. The results show that when the TiO2@Ag3 PO4 catalyst input amount is 0. 7 g/L,the Safranine dye wastewater’ s initial concentration was 70 mg/L,UV irradiation time was 35 min,the reaction temperature was 20 ℃,its cata-lytic degradation rate was up to 97. 9% and even after the catalyst was repeatedly used 5 times on end,its catalytic effect almost remained the same. Under the photophobic condition,catalyst of Safranine T 40 min maximum adsorption capacity is only 2. 3 mg/g. The reaction temperature is negatively related to the cata-lyst catalytic performance and high temperature catalytic will reduce its

  11. Energy Spectra of Geomagnetically Trapped Light Isotopes Measured by NINA-2 Instrument

    Science.gov (United States)

    Mikhailov, V. V.; Bakaldin, A.; Galper, A.; Koldashov, S.; Korotkov, M.; Leonov, A.; Voronov, S.; Bidoli, V.; Caoslino, M.; De Pascale, M.; Furano, G.; Iannucci, A.; Morselli, A.; Picozza, P.; Sparvoli, R.; Boezio, M.; Bonvincini, V.; Vacchi, A.; Zampa, N.; Ambriola, M.; Bellotti, R.; Cafagna, F.; Circella, M.; De Marzo, C.; Adriani, O.; Papini, P.; Spillantini, P.; Straulino, S.; Vannuccini, E.; Ricci, M.; Castellini, G.

    2003-07-01

    This paper reports about the energy spectrum of geomagnetically trapped protons, deuterons, tritons and He isotop es measured by the instrument NINA2 at the low boundary of the South Atlantic Anomaly. NINA-2 on board the satellite MITA has been in orbit from 15 July 2000 to 10 August 2001, flying with circular polar orbit (87° inclination), at an altitude between 300-440 km. Differential energy spectra were measured at L-shell ˜ 1.2 and local magnetic field b< 0.22 G. Data from NINA-2 are compared with measurements made onboard Resurs-01 N4 satellite with NINA instrument. Possible solar modulation effects are discussed.

  12. Observation of Trapped Light Isotopes By The Detectors Nina and Nina-2

    Science.gov (United States)

    Sparvoli, R.; Wizard/NINA Collaboration

    The detector NINA aboard the satellite Resurs-01-N4, and the following experiment NINA-2 aboard the spacecraft MITA, detected hydrogen and helium isotopes geomag- netically trapped, while crossing the South Atlantic Anomaly. Deuterium and tritium at L-shellMITA altitudes (respectively 800 km and 400 km), and for energy greater than 10 MeV/n, is the interaction of trapped protons with residual atmospheric helium. In addition, the comparison between NINA and NINA-2 data shows how the flux of trapped particles decreases with the increase of the solar activity.

  13. Light exotic isotopes: recent beam developments and physics applications at ISOLDE

    Energy Technology Data Exchange (ETDEWEB)

    Bergmann, U.C. E-mail: ucb@ifa.au.dk; Axelsson, L.; Bennett, J.R.J.; Borge, M.J.G.; Catherall, R.; Drumm, P.V.; Fedoseyev, V.N.; Forssen, C.; Fraile, L.M.; Fynbo, H.O.U.; Georg, U.; Giles, T.; Grevy, S.; Hornshoej, P.; Jonson, B.; Jonsson, O.C.; Koester, U.; Lettry, J.; Markenroth, K.; Marques, F.M.; Mishin, V.I.; Mukha, I.; Nilsson, T.; Nyman, G.; Oberstedt, A.; Ravn, H.L.; Riisager, K.; Schrieder, G.; Sebastian, V.; Simon, H.; Tengblad, O.; Wenander, F.; Wilhelmsen Rolander, K

    2002-04-22

    This paper is divided in three parts: (i) the measurement of yields and decay losses of Li and Be isotopes released from a thin foil tantalum target at the CERN/ISOLDE PS-Booster; (ii) results from {beta}-decay experiments on {sup 12}Be and {sup 14}Be, an improved half-life of 21.49(3) ms has been obtained for {sup 12}Be; (iii) the {beta}-decay of {sup 9}C. An outline of the analysis procedure to determine the branching at high excitation energies is given. The ground-state branch has been determined to 54.1(15)%.

  14. Preparation and Luminescence of Single-Host White-Light-Emitting BaSrMg(PO4)2 ∶ Eu2+ Phosphor for Ultraviolet LEDs%白光LED用单基质荧光粉BaSrMg( PO4)2∶Eu2+的制备及发光性能研究

    Institute of Scientific and Technical Information of China (English)

    潘再法; 刘爽; 朱澄静; 徐娟; 刘文涵; 王丽丽

    2011-01-01

    A single-host white-light-emitting phosphor BaSrMg(PO4)2:Eu2+ was prepared by high temperature solid-state reaction method, and the luminescence characteristics and XRD pattern were investigated. The results show that BaSrMg(PO1)2 phase was obtained by sintering at 1 200℃ for 3 hours. BaSrMg(PO4 )2: Eu2+ phosphor exhibits two main emission bands peaking at 424 and 585 nm, respectively. The emission band peaking at 424 nm is attributed to the 4f6 5d1→4f7 transition of Eu2+ substituting Sr2+ , while the emission band peaking at 585 nm originates from the 4f6 5d1→4f7 transition of Eu2+ replacing Ba2+ in host lattice. The excitation spectra of the two emission peaks are range from 250 to 400 nm and both peaking at 360 nm. The effect of the proportion of Ba and Sr, and the Eu2+ doping concentration on the emission intensity were discussed in detail. Different chromaticity coordinates were obtained for each phosphor, that is, the chromaticity coordinates of the designed phosphor is tunable for the white-emitting LED or for special purpose. Quantum efficiency was also examined for the phosphors with different Eu2+ doping concentration, and concentration quenching took place obviously when Eu2+ doping concentration was lager than 6% in mole ratio. The obtained phosphor BaSrMg(PO4)2 : Eu2+ can be excited by near ultraviolet radiation effectively and emit full color lighting, which is a promising single-host white-light-emitting phosphor for white LED.%采用高温固相反应法在1 200℃下制备了 Eu2+激活的BaSrMg( PO4)2高亮度白光荧光粉,并对其晶体结构和发光性能进行了研究.荧光光谱研究表明该荧光粉的发射光谱由两个谱带组成,其中心分别位于424和585 nm处,归结为Eu2+分别占据了基质中Sr2+,Ba2+格位而导致的4f 65d1→4f7电子跃迁.两个发射峰的激发光谱均分布在250~400nm的波长范围内,峰值位于360nm左右.表明该荧光粉可被INGaN管芯产生的近紫外辐射有效激发,是

  15. Insights from stable light isotopes on enamel defects and weaning in Pliocene herbivores

    Indian Academy of Sciences (India)

    Tamara A Franz-Odendaal; Julia A Lee-Thorp; Anusuya Chinsamy

    2003-12-01

    A high prevalence of enamel hypoplasia in several herbivores from the early Pliocene Langebaanweg locality, South Africa, indicates general systemic stress during the growing years of life. The presence of several linear enamel hypoplasias per tooth crown in many teeth further suggest that these stress events may be episodic. The 18O values along tooth crowns of mandibular second molars of Sivatherium hendeyi (Artiodactyla, Giraffidae) were used to investigate the cause of the stress events in this tooth type. Results show that weaning in this fossil giraffid occurred at a similar ontogenetic age to that in extant giraffes, and that the observed enamel hypoplasia towards the base of this tooth type manifested post-weaning. Further, high-resolution oxygen isotope analyses across S. hendeyi third molars suggest that the entire development of defective tooth crowns occurred under conditions of increased aridity in which the cool, rainy part of the seasonal cycle was missing. The high prevalence of this defect in many herbivores suggests that climatic conditions were not favourable. This study reiterates the value of stable isotope analyses in determining both the behaviour of fossil animals and the environmental conditions that prevailed during tooth development.

  16. The synthesis of the light Mo and Ru isotopes how now, no need for an exotic solution?

    CERN Document Server

    Costa, V; Zappalà, R A; Arnould, M

    2000-01-01

    The most detailed calculations of the p-process call for its development in the O/Ne layers of Type II supernovae. In spite of their overall success in reproducing the solar system content of p-nuclides, they suggest a significant underproduction of the light Mo and Ru isotopes. On grounds of a model for the explosion of a 25 solar mass star with solar metallicity, we demonstrate that this failure might just be related to the uncertainties left in the rate of the 22Ne(alpha,n)25Mg neutron producing reaction. The latter indeed have a direct impact on the distribution of the s-process seeds for the p-process.

  17. The synthesis of the light Mo and Ru isotopes: how now, no need for an exotic solution?

    Science.gov (United States)

    Costa, V.; Rayet, M.; Zappalà, R. A.; Arnould, M.

    2000-06-01

    The most detailed calculations of the p-process call for its development in the O/Ne layers of Type II supernovae. In spite of their overall success in reproducing the solar system content of p-nuclides, they suggest a significant underproduction of the light Mo and Ru isotopes. On grounds of a model for the explosion of a 25 Msun star with solar metallicity, we demonstrate that this failure might just be related to the uncertainties left in the rate of the \\reac{22}{Ne}{\\alpha}{n}{25}{Mg} neutron producing reaction. The latter indeed have a direct impact on the distribution of the s-process seeds for the p-process.

  18. Effects of Low-Molecular-Weight Organic Acids on the Dissolution of Hydroxyapatite Nanoparticles in Batch and Column Experiments: A Perspective from Phosphate Oxygen Isotope Fractionation

    Science.gov (United States)

    Wang, D.; Jaisi, D. P.; Jin, Y.

    2015-12-01

    Hydroxyapatite nanoparticles (HANPs) are increasingly being advocated as an efficient and environment-friendly "green" phosphorus nanofertilizer attributed to their nanoscale dimension, large reactive surface area, and low leaching potential. However, knowledge of how naturally occurring low-molecular-weight organic acids (LMWOAs) that are secreted by plant roots mediate the dissolution of HANPs (releasing PO43- ion for plant growth) is nonexistent. Here three most commonly encountered LMWOAs (acetic acid, oxalic acid, and citric acid) at environmentally relevant concentration (1 mM) were evaluated for their effects on HANPs' dissolution in static batch and dynamic column systems. Particularly, phosphate oxygen isotope fractionation of HANPs during dissolution was examined to disentangle mechanisms controlling the evolution of O-isotopic composition of dissolved PO43- ion. Our results reveal that in batch experiments the dissolution of HANPs was fast but the overall dissolution efficiency of HANPs was limited (≤30%). In contrast, ~100% HANPs were dissolved in columns where LMWOAs were continuously injected. The limited dissolution of HANPs in static batch systems was due primarily to pH buffer effect (pH increased sharply when LMWOA was added in HANPs suspension), whereas in dynamic column systems the HANPs were continuously dissolved by low pH LMWOAs and leached away. Regardless of LMWOA type and experimental system, the isotopically light phosphate (P16O4) was preferentially released during dissolution and the O-isotopic composition of dissolved PO43- ion increased gradually with increasing dissolution due to equilibrium isotope effect between dissolved PO43- ion and HANPs. However, the overall magnitude of O-isotopic fractionation of dissolved PO43- ion was less in batch than in column systems, due to less mass transfer between dissolved PO43- ions and HANPs in batch relative to column experiments. Our findings provide new insights into bioavailability

  19. Light Stable Isotopes in Aquifers Affected by Mining Activities in a Brazilian Mining Province

    Science.gov (United States)

    Moreira, R. M.; de Carvalho, J. B.

    2013-05-01

    Iron ore is presently a main item in the Brazilian commercial agenda. Large reserves have converted this utility into an important source of export earnings and, secondarily, of raw materials for the domestic industry. Parallel to a boom in mining activities in the last years environmental impacts and a stress on natural resources have soared. A region exhibiting pronouncedly intensive mining activities lies in the central part of the State of Minas Gerais, the third economy of the federation. Mines are sited right beside the capital and neighbor towns amounting to nearly five million inhabitants and a pronounced dependence on groundwater resources. Besides, this region is a water divide enclosing the sources of main contributors to the most strategic fluvial basins in the country. Iron ore is by large the main mineral but other metals (including gold and uranium), as well as non-metals such as limestone, quartz and granite, also occur. Given the significance of this commodity in the country's trade balance and the demand of water resources with acceptable quality for human consumption, the scale of ensuing water use conflicts caused by its exploration is wide ranging and has to be coped with well grounded environmental assessment approaches. Tracer hydrology techniques might be a valuable tool in this context. The characteristics of the area being impacted have been surveyed, including climate and pluviometry, stratigraphic litology, geological structure, use of soil, mineral resources and their exploration, surface and ground water hydrology and their sundry uses. Data to be processed have been procured at local public agencies but as regard local hydrological features, particularly isotopic compositions, ad hoc surveys and methodologies were required. One instance concerns pluviometric isotopy due to the alpine character of the surveyed region altitude and temperature effects might take place. Hence different sites were monitored; cumulative pluviometer samples

  20. [Preparation and luminescence characteristics of white-light emitting Ca9.95-xNa0.75K0.25(PO4)7: Eu0.05(2+), Mn(x)2+ phosphors].

    Science.gov (United States)

    Zhou, Guo-Xiong; Zhao, Wei-Ren; Song, En-Hai; Dou, Xi-Hua; Yi, Chun-Yu; Zhou, Min-Kang

    2011-08-01

    The Ca9.95-x Na0.75 K0.25 (PO4)7: Eu.0.05(2+), Mn(x)2+ (x = 0, 0.1, 0.2, 0.3, 0.4, 0.5, 0.6 and 0.7) phosphors were synthesized by high temperature solid-state reaction, and their phase composition and fluorescence emission properties were studied. Due to the existence of double phases with similar crystal structure, the 5d-4f transition of Eu2+ ions in the phosphors emits a fluorescence of wide wavelength with peaks located at 491 nm and 540 nm respectively. The energy transfer between Eu2+ and Mn2+, together with the occupation of Mn2+ ions at the eight coordination sites in the phosphors, makes the 4T1 (4G)-6A1 (6S) transition of Mn2+ ions eimit red emission peaked at 635 nm. The combination of fluorescence emtted by Mn2+ and Eu2+ ions results in the emission of white light with color coordinates (0.3335, 0.2924), (0.3999, 0.3179) and (0.3307, 0.2564). The nearly pure white light emitting makes the phosphors show great application potential in the white light-emitting LEDs.

  1. Production and decay spectroscopy of {sup 192}Po and {sup 194}Po

    Energy Technology Data Exchange (ETDEWEB)

    Andel, B., E-mail: boris.andel@fmph.uniba.sk [Department of Nuclear Physics and Biophysics, Comenius University in Bratislava, 842 48 Bratislava (Slovakia)

    2015-10-15

    A γ-ray spectroscopy study of the (11{sup −}) isomers in {sup 194}Po and {sup 192}Po was performed at the velocity filter SHIP at GSI (Germany). Nuclei were produced in fusion-evaporation reactions and investigated in the detection set-up at the focal plane after the separator. Several new γ transitions were attributed to the isomers and detailed analysis of the first γ-γ coincidences for both isomers is being prepared. For the reaction {sup 56}Fe + {sup 141}Pr → {sup 197}At*, excitation functions for astatine and polonium isotopes were measured and compared with HIVAP calculations.

  2. Light effects on the isotopic fractionation of skeletal oxygen and carbon in the cultured zooxanthellate coral, Acropora: implications for coral-growth rates

    Directory of Open Access Journals (Sweden)

    S. Reynaud

    2009-11-01

    Full Text Available Skeletal isotopic and metabolic measurements of the branching coral Acropora cultured in constant conditions and subjected to two light intensities were revisited. We individually compared the data recorded at low light (LL and high light (HL for 24 colonies, all derived from the same parent colony. Metabolic and isotopic responses to the different light levels were highly variable. High light led to productivity enhancement, reduction of surface extension, doubling of aragonite deposited weight and increased δ18O levels in all nubbins; responses in respiration and δ13C were not clear. The partitioning of the colonies into two groups, one showing a δ13C increase and the other a δ13C decrease with increased light, revealed common behaviors. Samples showing an increase in δ13C were associated with the co-variation of low surface extension and high productivity while samples showing a decrease in δ13C were associated with the co-variation of higher surface extension and limited productivity. This experiment, which allowed for the separation of temperature and light effects on the coral, highlighted the significant light influences on both skeletal δ18O and δ13C. The high scattering of inter-colony δ18O observed at one site could be due to the differing photosynthetic responses of symbiotic algal assemblages. The δ13C responses could also be related to differing algal distributions in different skeletal portions. Our results were compared to observations by Gladfelter on Acropora cervicornis (1982. Both set of results highlight the relationships between coral-growth rates, micro-structures and photosynthetic activity. It appears that extension growth and accretion are two separate growth modes, and accretion is light-enhanced while extension is light-repressed. There are multiple consequences of these findings for paleoclimatic reconstructions involving corals.

  3. Isotopic yield in the cold ternary fission of even-even ^sup 250-260^Cf isotopes with ^sup 14^C as light charged particle

    National Research Council Canada - National Science Library

    KP Santhosh; Sreejith Krishnan

    2017-01-01

    Within the unified ternary fission model (UTFM), the 14C accompanied cold ternary fission of even-even 250-260Cf isotopes has been studied, in which the interacting potential barrier is taken as the sum of Coulomb and proximity potential...

  4. Shape coexistence measurements in even-even neutron-deficient polonium isotopes by Coulomb excitation, using REX-ISOLDE and the Ge MINIBALL array

    CERN Multimedia

    Butler, P; Bastin, B; Kruecken, R; Voulot, D; Rahkila, P J; Orr, N A; Srebrny, J; Grahn, T; Clement, E; Paul, E S; Gernhaeuser, R A; Dorsival, A; Diriken, J V J; Huyse, M L; Iwanicki, J S

    The neutron-deficient polonium isotopes with two protons outside the closed Z=82 shell represent a set of nuclei with a rich spectrum of nucleus structure phenomena. While the onset of the deformation in the light Po isotopes is well established experimentally, questions remain concerning the sign of deformation and the magnitude of the mixing between different configurations. Furthermore, controversy is present with respect to the transition from the vibrational-like character of the heavier Po isotopes to the shape coexistence mode observed in the lighter Po isotopes. We propose to study this transition in the even-mass neutron-deficient $^{198,200,202}$Po isotopes by using post-accelerated beams from REX-ISOLDE and "safe"-energy Coulomb excitation. $\\gamma$- rays will be detected by the MINIBALL array. The measurements of the Coulomb excitation differential cross section will allow us to deduce both the transition and diagonal matrix elements for these nuclei and, combined with lifetime measurements, the s...

  5. Quality assurance and quality control in light stable isotope laboratories: A case study of Rio Grande, Texas, water samples

    Science.gov (United States)

    Coplen, T.B.; Qi, H.

    2009-01-01

    New isotope laboratories can achieve the goal of reporting the same isotopic composition within analytical uncertainty for the same material analysed decades apart by (1) writing their own acceptance testing procedures and putting them into their mass spectrometric or laser-based isotope-ratio equipment procurement contract, (2) requiring a manufacturer to demonstrate acceptable performance using all sample ports provided with the instrumentation, (3) for each medium to be analysed, prepare two local reference materials substantially different in isotopic composition to encompass the range in isotopic composition expected in the laboratory and calibrated them with isotopic reference materials available from the International Atomic Energy Agency (IAEA) or the US National Institute of Standards and Technology (NIST), (4) using the optimum storage containers (for water samples, sealing in glass ampoules that are sterilised after sealing is satisfactory), (5) interspersing among sample unknowns local laboratory isotopic reference materials daily (internationally distributed isotopic reference materials can be ordered at three-year intervals, and can be used for elemental analyser analyses and other analyses that consume less than 1 mg of material) - this process applies to H, C, N, O, and S isotope ratios, (6) calculating isotopic compositions of unknowns by normalising isotopic data to that of local reference materials, which have been calibrated to internationally distributed isotopic reference materials, (7) reporting results on scales normalised to internationally distributed isotopic reference materials (where they are available) and providing to sample submitters the isotopic compositions of internationally distributed isotopic reference materials of the same substance had they been analysed with unknowns, (8) providing an audit trail in the laboratory for analytical results - this trail commonly will be in electronic format and might include a laboratory

  6. Light effects on the isotopic fractionation of skeletal oxygen and carbon in the cultured zooxanthellate coral, Acropora: implications for coral-growth rates

    Directory of Open Access Journals (Sweden)

    S. Reynaud

    2010-03-01

    Full Text Available Skeletal isotopic and metabolic measurements of the branching coral Acropora cultured in constant conditions and subjected to two light intensities were revisited. We individually compared the data recorded at low light (LL and high light (HL for 24 colonies, all derived from the same parent colony. Metabolic and isotopic responses to the different light levels were highly variable. High light led to productivity enhancement, reduction of surface extension, doubling of aragonite deposited weight and increased δ18O levels in all nubbins; responses in respiration and δ13C were not clear. The partitioning of the colonies cultured at HL into two groups, one showing a δ13C enrichment and the other a δ13C decrease revealed common behaviors. Samples showing an increase in δ13C were associated with the co-variation of low surface extension and high productivity while samples showing a decrease in δ13C were associated with the co-variation of higher surface extension and limited productivity. This experiment, which allowed for the separation of temperature and light effects on the coral, highlighted the significant light influences on both skeletal δ18O and δ13C. The high scattering of inter-colony δ18O observed at one site could be due to the differing photosynthetic responses of symbiotic algal assemblages. We compared our results with observations by Gladfelter on Acropora cervicornis (1982. Both set of results highlight the relationships between coral-growth rates, micro-structures and photosynthetic activity. It appears that extension growth and skeleton thickening are two separate growth modes, and thickening is light-enhanced while extension is light-suppressed. There are multiple consequences of these findings for paleoclimatic reconstructions involving corals.

  7. Light effects on the isotopic fractionation of skeletal oxygen and carbon in the cultured zooxanthellate coral, Acropora: implications for coral-growth rates

    Science.gov (United States)

    Juillet-Leclerc, A.; Reynaud, S.

    2010-03-01

    Skeletal isotopic and metabolic measurements of the branching coral Acropora cultured in constant conditions and subjected to two light intensities were revisited. We individually compared the data recorded at low light (LL) and high light (HL) for 24 colonies, all derived from the same parent colony. Metabolic and isotopic responses to the different light levels were highly variable. High light led to productivity enhancement, reduction of surface extension, doubling of aragonite deposited weight and increased δ18O levels in all nubbins; responses in respiration and δ13C were not clear. The partitioning of the colonies cultured at HL into two groups, one showing a δ13C enrichment and the other a δ13C decrease revealed common behaviors. Samples showing an increase in δ13C were associated with the co-variation of low surface extension and high productivity while samples showing a decrease in δ13C were associated with the co-variation of higher surface extension and limited productivity. This experiment, which allowed for the separation of temperature and light effects on the coral, highlighted the significant light influences on both skeletal δ18O and δ13C. The high scattering of inter-colony δ18O observed at one site could be due to the differing photosynthetic responses of symbiotic algal assemblages. We compared our results with observations by Gladfelter on Acropora cervicornis (1982). Both set of results highlight the relationships between coral-growth rates, micro-structures and photosynthetic activity. It appears that extension growth and skeleton thickening are two separate growth modes, and thickening is light-enhanced while extension is light-suppressed. There are multiple consequences of these findings for paleoclimatic reconstructions involving corals.

  8. Optical and spectral studies on pure and europium doped olgite type Na(Sr,Ba)PO4 ceramics.

    Science.gov (United States)

    Jawaher, K Rackesh; Jagannathan, R; Das, S Jerome; Krishnan, S

    2015-04-05

    Europium ion doped olgite type Na(Sr,Ba)PO4 ceramics, a new generation of light emitting bulb, was prepared by a high temperature solid-state reaction method. The synthesized materials were subjected to various characterizations such as X-ray powder diffraction, Scanning electron microscopy and FT-IR spectra measurements. The EPR spectrum of the sample exhibits a well-resolved hyperfine structure of 151Eu2+ and 153Eu2+ isotopes and the g value has been calculated. Fluorescence spectra revealed that europium ions were present in divalent as well as in the trivalent oxidation states. The critical distance for energy transfer between Eu2+ and Eu2+ ion is calculated as 20Å, which is in good agreement with that of experimental data. The FTIR analysis reveals all the vibrations of PO4(3-) ions.

  9. Studies of {sup 194,195,197}Po

    Energy Technology Data Exchange (ETDEWEB)

    Carpenter, M.P.; Ahmad, I.; Crowell, B. [and others

    1995-08-01

    The energy systematics of low-lying polonium states show sudden changes near N = 114. The observed drops in the low-lying levels of {sup 196,198}Po relative to the heavier isotopes indicate significant changes in the underlying structure of these nuclei. It is thought that this change is due to the onset of vibrational collectivity brought about by the quadrupole interaction between neutron and proton-pairs. In order to extend the Po systematics even further, we measured, for the first time, states in {sup 194,195,197}Po using the {sup 28}Si + {sup 170}Yb reaction at a beam energy of 142 MeV. The beam was supplied by ATLAS, and the data were taken with 10 Compton-suppressed Ge detectors placed at the target position of the Fragment Mass Analyzer. Preliminary level schemes were constructed for {sup 194,195,197}Po based on {gamma}-{gamma} and {gamma}-FMA coincidences. The results for {sup 194}Po show that the 2{sup +} - 0{sup +} transition energy decreased in energy by 140 keV relative to {sup 196}Po suggesting that this nucleus moved beyond the vibrational limit to more collective motion. An extrapolation of the systematics predicts that the 2{sup +} energy could drop another 140 keV between {sup 194}Po and {sup 192}Po which would indicate the onset of rotational motion. Currently, we have an approved experiment to investigate the decay of yrast isomers in {sup 194}Po which will allow us to (1) confirm our earlier level scheme of {sup 194}Po, and (2) assess the experimental conditions needed for a future study of {sup 192}Po.

  10. Provenancing Archaeological Wool Textiles from Medieval Northern Europe by Light Stable Isotope Analysis (δ13C, δ15N, δ2H)

    Science.gov (United States)

    von Holstein, Isabella C. C.; Walton Rogers, Penelope; Craig, Oliver E.; Penkman, Kirsty E. H.; Newton, Jason; Collins, Matthew J.

    2016-01-01

    We investigate the origin of archaeological wool textiles preserved by anoxic waterlogging from seven medieval archaeological deposits in north-western Europe (c. 700–1600 AD), using geospatial patterning in carbon (δ13C), nitrogen (δ15N) and non-exchangeable hydrogen (δ2H) composition of modern and ancient sheep proteins. δ13C, δ15N and δ2H values from archaeological wool keratin (n = 83) and bone collagen (n = 59) from four sites were interpreted with reference to the composition of modern sheep wool from the same regions. The isotopic composition of wool and bone collagen samples clustered strongly by settlement; inter-regional relationships were largely parallel in modern and ancient samples, though landscape change was also significant. Degradation in archaeological wool samples, examined by elemental and amino acid composition, was greater in samples from Iceland (Reykholt) than in samples from north-east England (York, Newcastle) or northern Germany (Hessens). A nominal assignment approach was used to classify textiles into local/non-local at each site, based on maximal estimates of isotopic variability in modern sheep wool. Light element stable isotope analysis provided new insights into the origins of wool textiles, and demonstrates that isotopic provenancing of keratin preserved in anoxic waterlogged contexts is feasible. We also demonstrate the utility of δ2H analysis to understand the location of origin of archaeological protein samples. PMID:27764106

  11. Isotopically light carbon dioxide in nitrogen rich gases: the gas distribution pattern in the French Massif Central, the Eifel and the western Eger Rift

    Directory of Open Access Journals (Sweden)

    F. H. Weinlich

    2005-06-01

    Full Text Available Based on characteristics of the distribution pattern of the western Eger Rift spring gases, a distribution pattern is presented for the gases of the French Massif Central. The central parts of these areas with ascending magmatic CO2 are characterised by high gas fluxes, high CO2 contents of up to 99.99 vol% and isotopially heavy CO2. In the peripheries, the decrease of d13C values of CO2 and CO2 contents in the gas phase is compensated by a rise in N2 contents. It can be demonstrated that gas fractionation in contrary to mixtures with isotopically light biogenic or crustal CO2 controls the distribution pattern of gas composition and isotopic composition of CO2 in these spring gases. Dissolution of CO2 results in formation of HCO3 ? causing isotope fractionation of CO2 and an enrichment of N2 in the gas phase. With multiple equilibrations, values of about ?17 ? or lower are obtained. The scale of gas alteration depends on the gas flux and the gas-water ratios respectively and can result in N2-rich gases. Essential for the interpretation are gas flux measurements with mass balances derived for most of the springs. Without such mass balances it is not possible to discriminate between mixture and fractionation. The processes of isotopic and chemical solubility fractionations evidently control the gas distribution pattern in other regions as well.

  12. Variation of the light stable isotopes in the superior and inferior grains of rice (Oryza sativa L.) with different geographical origins.

    Science.gov (United States)

    Chen, Tianjin; Zhao, Yan; Zhang, Weixing; Yang, Shuming; Ye, Zhihua; Zhang, Guoyou

    2016-10-15

    Trying to explore a new research angle to increase the resolution and accessibility of isotopic based traceability technique, light stable isotopes (δ(13)C, δ(15)N, δD and δ(18)O) in the superior (SS) and inferior (IS) grains of a rice cultivar Daohuaxiang were analyzed with relatively limited sample numbers and adjacent sites in Fujin and Wuchang, Heilongjiang Province, PR China. Distribution of δ(13)C, δ(15)N and δ(18)O in the SS and IS grains were found to be different. δ(18)O and δD can discriminate rice cultivation areas. However, δ(13)C and δ(15)N values in Fujin and Wuchang overlapped when the differences between SS and IS were considered, thus δ(13)C and δ(15)N cannot be used to discriminate cultivation areas. This exploratory study indicate the variation of the light stable isotopes in the grains located on different panicle positions could be used to discriminate the geographical origin but still need further systematic consideration and verification.

  13. po_stack_movie

    DEFF Research Database (Denmark)

    2009-01-01

    po_stack® er et reolsystem, hvis enkle elementer giver stor flexibilitet, variation og skulpturel virkning. Elementerne stables og forskydes frit, så reolens rum kan vendes til begge sider, være åbne eller lukkede og farvekombineres ubegrænset. Reolen kan let ombygges, udvides eller opdeles, når ...

  14. Determination of 210Pb, 210Po, 226Ra, 228Ra and uranium isotopes in drinking water in order to comply with the requirements of the EU ‘Drinking Water Directive.

    Science.gov (United States)

    Vasile, M; Loots, H; Jacobs, K; Verheyen, L; Sneyers, L; Verrezen, F; Bruggeman, M

    2016-03-01

    The European Union published in 2013 a new Drinking Water Directive with stricter requirements for measuring natural radioactivity. In order to adhere to this, a method for sequential separation of 210Pb, 210Po, 238U and 234U in drinking water was applied using UTEVA® and Sr resins. Polonium-210, 238U and 234U were quantified using alpha-particle spectrometry and 210Pb using liquid scintillation counting. Radium-226 and 228Ra were determined using 3M Empore Radium RAD Disks, and their quantification was done using a Quantulus™ 1220 liquid scintillation counter.

  15. Lighting

    Data.gov (United States)

    Federal Laboratory Consortium — Lighting Systems Test Facilities aid research that improves the energy efficiency of lighting systems. • Gonio-Photometer: Measures illuminance from each portion of...

  16. Light

    DEFF Research Database (Denmark)

    Prescott, N.B.; Kristensen, Helle Halkjær; Wathes, C.M.

    2004-01-01

    This chapter presents the effect of artificial light environments (light levels, colour, photoperiod and flicker) on the welfare of broilers in terms of vision, behaviour, lameness and mortality......This chapter presents the effect of artificial light environments (light levels, colour, photoperiod and flicker) on the welfare of broilers in terms of vision, behaviour, lameness and mortality...

  17. Momentum transport cross-section measurements for potassium and rubidium in rare gases and white light-induced separation of rubidium isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Mugglin, D.T.

    1993-12-31

    This dissertation is concerned with two light-induced kinetic effects, light-induced diffusive pulling and light-induced drift. We use a light-induced diffusive pulling experiment to measure the ground state velocity-changing collision cross section (related to the momentum transport cross section and the diffusion coefficient) and the relative difference ({Delta}{sigma}/{sigma}) of the excited and ground state cross sections with respect to that of the ground state for potassium mixed with inert buffer gases. The measured excited state cross section is a weighted average of the potassium 4{sup 2}P{sub 1/2} and 4{sup 2}P{sub 3/2} fine structure levels, which are mixed by collisions with inert gas atoms. For the ground state cross sections, we obtain the following experimental results for potassium mixed with He, Ne, Ar, Kr, and Xe, respectively: 52 {+-} 4, 57 {+-} 8, 61 {+-} 5, 43 {+-} 5, and 60 {+-}5 {angstrom}{sup 2}. For {Delta}{sigma}/{sigma}, we obtain the following (in the same order): 0.085 {+-} 0.010, 0.058 {+-} 0.006, 0.41 {+-} 0.03, 0.43 {+-} 0.03, and 0.61 {+-} 0.05. For potassium-Ne and potassium-Ar, we combine these measurements with light-induced drift measurements of the ratio {Delta}{sigma}(J = 3/2) : {Delta}{sigma}(J = 1/2) to obtain absolute transport cross sections for the individual 4{sup 2}S{sub 1/2}, 4{sup 2}P{sub 1/2}, and 4{sup 2}P{sub 3/2} levels. We also use the light-induced diffusive pulling experimental method to measure {Delta}{sigma}/{sigma} for Rb-inert gas mixtures. We obtain values for the ground state diffusion cross section for Rb in several of the inert gases as well. We report the first experimental observation of the separation of two isotopes using broadband light by the process of white light-induced drift. For a light source, we use a broadband laser with an acousto-optic modulator as an output coupler. We verify the separation of the {sup 85}Rb and {sup 87}Rb isotopes.

  18. KPr(PO34

    Directory of Open Access Journals (Sweden)

    Abdelghani Oudahmane

    2010-08-01

    Full Text Available Single crystals of the title compound, potassium praseodymium(III polyphosphate, were obtained by solid-state reaction. The monoclinic non-centrosymmetric structure is isotypic with all other KLn(PO34 analogues from Ln = La to Er, inclusive. The crystal structure of these long-chain polyphosphates is built up from infinite crenelated polyphosphate chains of corner-sharing PO4 tetrahedra with a repeating unit of four tetrahedra. These chains, running along [100], are arranged in a pseudo-tetragonal rod packing and are further linked by isolated PrO8 square antiprisms [Pr—O = 2.3787 (9–2.5091 (8 Å], forming a three-dimensional framework. The K+ ions reside in channels parallel to [010] and exhibit a highly distorted coordination sphere by eight O atoms at distances ranging from 2.7908 (9 to 3.1924 (11 Å.

  19. Luminescence properties of Ce{sup 3+} co-activated LaPO{sub 4}:Dy{sup 3+} nanorods prepared in different solvents and tunable blue to white light emission from Eu{sup 3+} co-activated LaPO{sub 4}:Dy{sup 3+}, Ce{sup 3+}

    Energy Technology Data Exchange (ETDEWEB)

    Phaomei, Ganngam [Department of Chemistry, Manipur University, Manipur 795003 (India); Rameshwor Singh, W., E-mail: dr.rmsingh@yahoo.co.in [Department of Chemistry, Manipur University, Manipur 795003 (India); Shanta Singh, N. [Department of Physics, Manipur University, Manipur 795003 (India); Ningthoujam, R.S., E-mail: nraghu_mani@yahoo.co.in [Chemistry Division, Bhabha Atomic Research Center, Mumbai 400085 (India)

    2013-02-15

    The nanorods of Ce{sup 3+} sensitized LaPO{sub 4}:Dy{sup 3+} with and without co-activation of Eu{sup 3+} have been synthesized by simple chemical route at relatively low temperature (150 Degree-Sign C). Effect of solvents on photoluminescence properties of Ce{sup 3+} sensitized LaPO{sub 4}:Dy{sup 3+} is studied by taking different solvents such as water, ethylene glycol (EG), dimethyl sulfoxide (DMSO) and their mixture. The samples prepared in EG and DMSO show monoclinic phase, whereas the samples prepared in water and mixed solvents show hexagonal phase. This hexagonal phase is transformed to monoclinic phase when the sample is heated at or above 600 Degree-Sign C and exhibits less luminescence intensity than that in monoclinic phase. The luminescence intensity of Dy{sup 3+} is enhanced when co-doped with Ce{sup 3+} because of energy transfer process. The luminescence color can be tuned from blue to white when Eu{sup 3+} is co-doped into LaPO{sub 4}:Dy{sup 3+}, Ce{sup 3+}. The prepared nanoparticles are dispersible and their polymer films are prepared after incorporation in to the polymer matrix. - Graphical Abstract: White emission production from Ce{sup 3+} sensitized LaPO{sub 4}:Dy{sup 3+}, Eu{sup 3+} nanorods. Highlights: Black-Right-Pointing-Pointer Synthesis of Ce{sup 3+} sensitized LaPO{sub 4}:Dy{sup 3+} nanorods. Black-Right-Pointing-Pointer Photoluminescence properties of samples prepared in different solvents. Black-Right-Pointing-Pointer Tuning of color from blue to white on co-doping of Eu{sup 3+} in LaPO{sub 4}:Dy{sup 3+}, Ce{sup 3+}. Black-Right-Pointing-Pointer Dispersion of particles in polar medium. Black-Right-Pointing-Pointer Polymer based film formation.

  20. Shape coexistence in krypton and selenium light isotopes studied through Coulomb excitation of radioactive ions beams; Etude de la coexistence de formes dans les isotopes legers du krypton et du selenium par excitation Coulombienne de faisceaux radioactifs

    Energy Technology Data Exchange (ETDEWEB)

    Clement, E

    2006-06-15

    The light krypton isotopes show two minima in their potential energy corresponding to elongated (prolate) and compressed (oblate) quadrupole deformation. Both configuration are almost equally bound and occur within an energy range of less than 1 MeV. Such phenomenon is called shape coexistence. An inversion of the ground state deformation from prolate in Kr{sup 78} to oblate in Kr{sup 72} with strong mixing of the configurations in Kr{sup 74} and Kr{sup 76} was proposed based on the systematic of isotopic chain. Coulomb excitation experiments are sensitive to the quadrupole moment. Coulomb excitation experiments of radioactive Kr{sup 74} and Kr{sup 76} beam were performed at GANIL using the SPIRAL facility and the EXOGAM spectrometer. The analysis of these experiments resulted in a complete description of the transition strength and quadrupole moments of the low-lying states. They establish the prolate character of the ground state and an oblate excited state. A complementary lifetime measurement using a 'plunger' device was also performed. Transition strength in neighboring nuclei were measured using the technique of intermediate energy Coulomb excitation at GANIL. The results on the Se{sup 68} nucleus show a sharp change in structure with respects to heavier neighboring nuclei. (author)

  1. Isotopic microanalysis sheds light on the magmatic endmembers feeding volcanic eruptions: The Astroni 6 case study (Campi Flegrei, Italy)

    Science.gov (United States)

    Arienzo, I.; D'Antonio, M.; Di Renzo, V.; Tonarini, S.; Minolfi, G.; Orsi, G.; Carandente, A.; Belviso, P.; Civetta, L.

    2015-10-01

    Sr-isotopic microanalysis has been performed on selected minerals from the Campi Flegrei caldera, together with Sr and Nd isotopic ratio determinations on bulk mineral and glass fractions. The aim was a better characterization of the chemically homogeneous, but isotopically distinct magmatic components which fed volcanic eruptions of the caldera over the past 5 ka, in order to enhance our knowledge about one of the most dangerous volcanoes on Earth. Information on the involved magmatic endmembers, unobtainable by analyzing the isotopic composition of whole rock samples and bulk mineral fractions, has been acquired through high-precision determination of 87Sr/86Sr on single crystals and microdrilled mineral powders. We focused our investigations on the products emplaced during the Astroni 6 eruption (4.23 cal ka BP), assumed representative of the expected event in case of renewed volcanic activity in the Campi Flegrei caldera. Data on single crystals and microdrilled mineral powders have been compared with Sr and Nd isotopic compositions of bulk mineral fractions from products emplaced during the whole Astroni activity, which included seven distinct eruptions. The 87Sr/86Sr ratios of single crystals and microdrilled mineral powders are in the 0.7060 to 0.7076 range, much wider than that of bulk mineral fractions, which range from 0.7066 to 0.7076. Moreover, the Sr isotopic ratios are inversely correlated to 143Nd/144Nd. The new data allow us to better define the magmatic endmembers involved in mingling/mixing processes that occurred prior to/during the Astroni activity. One magmatic endmember, characterized by average 87Sr/86Sr ratio of ~ 0.70750, was quite common in the past 15 ka activity of the Campi Flegrei caldera; the other, as evidenced by the isotopic composition of single feldspar and clinopyroxene crystals, is less enriched in radiogenic Sr (87Sr/86Sr ~ 0.70724). The latter is interpreted to represent a new magmatic component that entered the Campi Flegrei

  2. Electronic structure and photoluminescence properties of yellow-emitting Ca{sub 10}Na(PO{sub 4}){sub 7}: Eu{sup 2+} phosphor for white light-emitting diodes

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Hua [College of Materials and Environmental Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China); Deng, Degang; Li, Yinqun [College of Materials Science and Engineering, China Jiliang University, Hangzhou 310018 (China); Xu, Shiqing, E-mail: sxucjlu@hotmail.com [College of Materials Science and Engineering, China Jiliang University, Hangzhou 310018 (China); Li, Yinyan [College of Materials Science and Engineering, China Jiliang University, Hangzhou 310018 (China); Key Laboratory of Rare Earth Chemistry and Physics, State Key Laboratory of Polymer Physics and Chemistry, and State Key Laboratory of Electro analytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Yu, Cuiping; Ding, Yanyan; Lu, Hongwei; Yin, Haoyong; Nie, Qiulin [College of Materials and Environmental Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China)

    2013-11-15

    The yellow-emitting Ca{sub 10}Na(PO{sub 4}){sub 7}:Eu{sup 2+} phosphors were synthesized by conventional high-temperature solid-state reaction method. The phosphors were well characterized by powder X-ray diffraction, FT-IR spectra and diffuse reflectance spectra. DFT calculation results showed that Ca{sub 10}Na(PO{sub 4}){sub 7} had an indirect bandgap with a bandgap energy of about 3.82 eV. Ca{sub 10}Na(PO{sub 4}){sub 7}:Eu{sup 2+} showed a yellow emission band peaking at 550 nm under 350 nm excitation. The broad emission bandwidth (about 138 nm) of Ca{sub 10}Na(PO{sub 4}){sub 7}:Eu{sup 2+} is favorable for white LEDs conversion phosphors. The optimal doping concentration of Eu{sup 2+} ions in Ca{sub 10}Na(PO{sub 4}){sub 7}:Eu{sup 2+} phosphor was about 8 mol%. This study demonstrated that the energy transfer among the nearest-neighbor ions was the main mechanism of concentration quenching of Ca{sub 10}Na(PO{sub 4}){sub 7}:Eu{sup 2+} phosphor. These results indicate that Ca{sub 10}Na(PO{sub 4}){sub 7}:Eu{sup 2+} may be potentially useful as a UV radiation-converting phosphor for white LEDs. -- Highlights: • A yellow-emitting phosphor Ca{sub 10}Na(PO{sub 4}){sub 7}:Eu{sup 2+} was synthesized by solid-state reaction. • Ca{sub 10}Na(PO{sub 4}){sub 7}, with a large bandgap of about 3.82 eV, was a good host for luminescent ions. • The excitation band from 280 nm to 475 nm matched well with the emission of UV-LEDs. • The wide emission bandwidth (FWHM≈138 nm) of the phosphor was favorable for white LEDs.

  3. Biogeochemical factors affecting the presence of 210Po in groundwater

    Science.gov (United States)

    Seiler, R.L.; Stillings, L.L.; Cutler, N.; Salonen, L.; Outola, I.

    2011-01-01

    The discovery of natural 210Po enrichment at levels exceeding 500 mBq/L in numerous domestic wells in northern Nevada, USA, led to a geochemical investigation of the processes responsible for its mobilization. 210Po activities in 63 domestic and public-supply wells ranged from below 1 mBq/L to 6590 ± 590 mBq/L, among the highest reported levels in the USA. There is little spatial or depth variability in 210Pb activity in study-area sediments and mobilization of a few percent of the 210Po in the sediments would account for all of the 210Po in water. Stable-isotope measurements indicate SO4 reduction has occurred in all 210Po contaminated wells. Sulfide species are not accumulating in the groundwater in much of Lahontan Valley, probably because of S cycling involving microbial SO4 reduction, abiotic oxidation of H2S to S0 by Mn(IV), followed by microbial disproportionation of S0 to H2S and SO4. The high pH, Ca depletion, MnCO3 saturation, and presence of S0 in Lahontan Valley groundwater may be consequences of the anaerobic S cycling. Consistent with data from naturally-enriched wells in Florida, 210Po activities begin to decrease when aqueous sulfide species begin to accumulate. This may be due to formation and precipitation of PoS, however, Eh–pH diagrams suggest PoS would not be stable in study-area groundwater. An alternative explanation for the study area is that H2S accumulation begins when anaerobic S cycling stops because Mn oxides are depleted and their reduction is no longer releasing 210Po. Common features of 210Po-enriched groundwater were identified by comparing the radiological and geochemical data from Nevada with data from naturally-enriched wells in Finland, and Florida and Maryland in the USA. Values of pH ranged from 9 in Nevada wells, indicating that pH is not critical in determining whether 210Po is present. Where U is present in the sediments, the data suggest 210Po levels may be elevated in aquifers with (1) SO4-reducing waters with low H2S

  4. Enhanced photo-stability and photocatalytic activity of Ag3PO4 via modification with BiPO4 and polypyrrole

    Science.gov (United States)

    Cai, Li; Jiang, Hui; Wang, Luxi

    2017-10-01

    Ag3PO4 photocatalysts modified with BiPO4 and polypyrrole (PPy) were successfully synthesized via a combination of co-precipitation hydrothermal technique and oxidative polymerization method. Their morphologies, structures and optical and electronic properties were characterized by means of scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), transmission electron microscope (TEM), Brunauer-Emmett-Teller (BET) surface areas, X-ray diffraction (XRD), fourier transform infrared spectra (FT-IR), X-ray photo-electron spectroscopy (XPS), UV-vis diffuse reflection spectra (UV-vis DRS), photocurrent technique and electrochemical impedance spectra (EIS). The typical triphenylmethane dye (malachite green) was chosen as a target organic contaminants to estimate the photocatalytic activities and photo-stabilities of Ag3PO4-BiPO4-PPy heterostructures under visible light irradiation. The results indicated that the existence of BiPO4 and PPy not only showed great influences on the photocatalytic activity, but also significantly enhanced photo-stability of Ag3PO4 in repeated and long-term applications. The degradation conversion of Ag3PO4-BiPO4-PPy heterostructures (ABP-3) was 1.58 times of that of pure Ag3PO4. The photo-corrosion phenomenon of Ag3PO4 was effectively avoided. The photocatalytic activity of up to 87% in the Ag3PO4-BiPO4-PPy heterostructures (ABP-3) can be remained after five repeated cycles, while only about 33% of the degradation efficiency can be reserved in pure Ag3PO4. The possible mechanism of enhanced photo-stability and photocatalytic activity of Ag3PO4-BiPO4-PPy heterostructures was also discussed in this work.

  5. An episode of widespread ocean anoxia during the latest Ediacaran Period revealed by light U isotope compositions in carbonates

    Science.gov (United States)

    Zhang, F.

    2015-12-01

    Reconstruction of ocean redox chemistry during the Ediacaran Period is important for understanding the causal relationship between environmental oxygen levels and early metazoan evolution. Geochemical data (e.g., high Mo and U concentrations and/or heavy Mo and U isotope compositions from sedimentary rocks) provide evidence of extensive ocean oxygenation shortly after the Marinoan glaciation at ca. 632 Ma [1], during the late Ediacaran Period at ca. 560-551 Ma [2], and multiple times during the early Cambrian Period [3, 4]. These episodes of oxygenation may have been separated by intervals of less oxygenated conditions [1, 2]. However, the global redox state of the ocean during the terminal Ediacaran period (ca. 551-541 Ma) is poorly constrained. We address this knowledge gap by measuring carbonate U isotope compositions (δ238U) - a novel global ocean redox proxy - of the Gaojiashan Member of the late Ediacaran Dengying Formation (ca. 551-541 Ma) in South China. An abrupt negative shift in δ238U from values scattering around -0.45‰ to values averaging -0.95‰ (±0.20‰, 2sd) was observed in the middle Gaojiashan Member, suggesting a globally widespread expansion of ocean anoxia during the terminal Ediacaran Period. The negative δ238U shift coincides with the onset of a pronounced positive carbon isotope excursion (from 0‰ to +6‰), suggesting that ocean anoxia is the major driving force behind enhanced organic carbon burial that led to the carbon isotope excursion. The widespread anoxia recorded by the Gaojiashan Member is bracketed by known intervals of extensive ocean oxygenation, thus indicating that the Precambrian-Phanerozoic transition was characterized by oscillating ocean redox conditions. The Ediacara biota (ca. 541 Ma) [5] disappeared shortly after the widespread ocean anoxia, suggesting that an expansion of ocean anoxia may have triggerred the onset of a mass extinction in the latest Ediacaran time. References: [1] Sahoo, et al. (2012), Nature

  6. Silicon isotope separation utilizing infrared multiphoton dissociation of Si{sub 2}F{sub 6} irradiated with two-color CO{sub 2} laser light

    Energy Technology Data Exchange (ETDEWEB)

    Yokoyama, Atsushi; Ohba, Hironori; Hashimoto, Masashi [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment; Ishii, Takeshi; Ohya, Akio [Nuclear Development Corp., Tokai, Ibaraki (Japan); Arai, Shigeyoshi [Hill Research Co. Ltd., Tokyo (Japan)

    2002-08-01

    Silicon isotope separation has been done by utilizing the Infrared Multiphoton Dissociation (IRMPD) of Si{sub 2}F{sub 6} irradiated with two-color CO{sub 2} laser lights. The two-color excitation method improved the separation efficiency keeping the high enrichment factors. For example, 99.74% of {sup 28}Si was obtained at 49.63% dissociation of Si{sub 2}F{sub 6} after the simultaneous irradiation of 200 pulses with 966.23 cm{sup -1} photons (0.084 J/cm{sup 2}) and 954.55 cm{sup -1} photons (0.658 J/cm{sup 2}), while 2000 pulses were needed to obtain 99.35% of {sup 28}Si at 35.6% dissociation in the case of only one-color irradiation at 954.55 cm{sup -1} (0.97 J/cm{sup 2}). (author)

  7. Light

    CERN Document Server

    Robertson, William C

    2003-01-01

    Why is left right and right left in the mirror? Baffled by the basics of reflection and refraction? Wondering just how the eye works? If you have trouble teaching concepts about light that you don t fully grasp yourself, get help from a book that s both scientifically accurate and entertaining with Light. By combining clear explanations, clever drawings, and activities that use easy-to-find materials, this book covers what science teachers and parents need to know to teach about light with confidence. It uses ray, wave, and particle models of light to explain the basics of reflection and refraction, optical instruments, polarization of light, and interference and diffraction. There s also an entire chapter on how the eye works. Each chapter ends with a Summary and Applications section that reinforces concepts with everyday examples. Whether you need a deeper understanding of how light bends or a good explanation of why the sky is blue, you ll find Light more illuminating and accessible than a college textbook...

  8. Synthesis, luminescent properties and white light emitting diode application of Ba{sub 7}Zr(PO{sub 4}){sub 6}:Eu{sup 2+} yellow-emitting phosphor

    Energy Technology Data Exchange (ETDEWEB)

    Li, Chenxia; Dai, Jian [College of Optical and Electronic Technology, China Jiliang University, Hangzhou 310018 (China); Deng, Degang, E-mail: dengdegang@cjlu.edu.cn [College of Materials Science and Engineering, China Jiliang University, Hangzhou 310018 (China); Shen, Changyu [College of Optical and Electronic Technology, China Jiliang University, Hangzhou 310018 (China); Xu, Shiqing, E-mail: sxucjlu@163.com [College of Materials Science and Engineering, China Jiliang University, Hangzhou 310018 (China)

    2015-10-15

    A yellow-emitting phosphor, Eu{sup 2+}-activated Ba{sub 7}Zr(PO{sub 4}){sub 6} phosphor was synthesized by solid-state reaction method and the luminescence properties were investigated. The phosphor exhibited strong absorption in near ultraviolet (n-UV) region, which matched well with the n-UV chip. Upon excitation at 370 nm, the Ba{sub 7}Zr(PO{sub 4}){sub 6}:Eu{sup 2+} phosphor has a broad yellow emission band with a peak at 585 nm and a full width at half maximum of 178 nm wider than that of the commercial yellow-emitting YAG:Ce{sup 3+} phosphor. The mechanism of concentration quenching of Eu{sup 2+} ions in Ba{sub 7}Zr(PO{sub 4}){sub 6} phosphor is verified to be energy transfer among the nearest neighbor Eu{sup 2+} ions. The CIE value and temperature dependence of photoluminescence were also discussed. Furthermore, a white-LED was fabricated using a 370 nm UV chip pumped with a blend of phosphors consisting of yellow-emitting Ba{sub 6.97}Zr(PO{sub 4}){sub 6}:0.03Eu{sup 2+} and blue-emitting BaMgAl{sub 10}O{sub 17}:Eu{sup 2+} phosphors, which achieved a CIE of (0.3329, 0.3562) with a color-rendering index of 86.4 around the CCT of 5487 K.

  9. A novel white emitting phosphor of Dy{sup 3+} doped Ca{sub 19}Mg{sub 2}(PO{sub 4}){sub 14} for light-emitting diodes

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Ge; Wang, Yuhua, E-mail: wyh@lzu.edu.cn; Wang, Qian; Ding, Xin; Geng, Wanying; Shi, Yurong

    2014-10-15

    A series of Dy{sup 3+} doped Ca{sub 19}Mg{sub 2}(PO{sub 4}){sub 14} phosphors were firstly synthesized by the solid-state reaction method. The phase purity and characteristic luminescent properties are investigated in detail by X-ray diffraction refinement, photoluminescence spectra and decay times measurement. Under 365 nm excitation, Ca{sub 19}Mg{sub 2}(PO{sub 4}){sub 14}:Dy{sup 3+} phosphor can exhibit intense warm white emission with CIE chromaticity coordinates (0.400, 0.452) and low correlated color temperature (3994 K). The optimal doping contents of Dy{sup 3+} in Ca{sub 19}Mg{sub 2}(PO{sub 4}){sub 14} is determined to be 2%. The thermal quenching property of Ca{sub 19}Mg{sub 2}(PO{sub 4}){sub 14}:Dy{sup 3+} is also investigated and it remains 60% of the initial emission intensity even when the temperature increases to 230 °C. The results show that Ca{sub 19}Mg{sub 2}(PO{sub 4}){sub 14}:Dy{sup 3+} can be a promising single phased white emitting phosphor for UV white LEDs. - Highlights: • A series of Dy{sup 3+} doped CMP phosphors were successfully synthesized. • The phase purity and characteristic photoluminescence properties were investigated. • CMP:Dy{sup 3+} phosphor exhibits warm white emission with CIE (0.400, 0.452) and low CCT (3994 K). • CMP:Dy{sup 3+} phosphor has good thermal stability.

  10. Study on preparation and performances of CDPVC/Ag3PO4 composite photocatalyst

    Directory of Open Access Journals (Sweden)

    Peng WANG

    2016-04-01

    Full Text Available PVC/Ag3PO4 composites are prepared by solution-dipping method, and the as-prepared composites are heat-treated to release HCl from PVC molecules to obtain conjugated derivative of PVC/Ag3PO4(CDPVC/Ag3PO4 composites. The CDPVC/Ag3PO4 composites are characterized by XRD, SEM, UV-vis DRS, PL and XPS. The effects of preparation conditions on the visible-light photocatalytic performances of CDPVC/Ag3PO4 composites are investigated by evaluating the decomposition of methyl orange under visible light irradiation. The results reveal that the modification of CDPVC is beneficial to the dispersion of Ag3PO4 particles, and it can obviously improve the absorbance of the CDPVC/Ag3PO4 composites in the range of visible light and the charge separation efficiency. The CDPVC/Ag3PO4 composites exhibit excellent visible-light photocatalytic acitivity and stability when the mass percentage of PVC to Ag3PO4, heat-treatment temperature and time are 0.03%, 130 ℃, and 2 h, respectively.

  11. RAPID DETERMINATION OF {sup 210} PO IN WATER SAMPLES

    Energy Technology Data Exchange (ETDEWEB)

    Maxwell, S.

    2013-05-22

    A new rapid method for the determination of {sup 210}Po in water samples has been developed at the Savannah River National Laboratory (SRNL) that can be used for emergency response or routine water analyses. If a radiological dispersive device (RDD) event or a radiological attack associated with drinking water supplies occurs, there will be an urgent need for rapid analyses of water samples, including drinking water, ground water and other water effluents. Current analytical methods for the assay of {sup 210}Po in water samples have typically involved spontaneous auto-deposition of {sup 210}Po onto silver or other metal disks followed by counting by alpha spectrometry. The auto-deposition times range from 90 minutes to 24 hours or more, at times with yields that may be less than desirable. If sample interferences are present, decreased yields and degraded alpha spectrums can occur due to unpredictable thickening in the deposited layer. Separation methods have focused on the use of Sr Resin, often in combination with 210Pb analysis. A new rapid method for {sup 210}Po in water samples has been developed at the Savannah River National Laboratory (SRNL) that utilizes a rapid calcium phosphate co-precipitation method, separation using DGA Resin (N,N,N,N-tetraoctyldiglycolamide extractant-coated resin, Eichrom Technologies or Triskem-International), followed by rapid microprecipitation of {sup 210}Po using bismuth phosphate for counting by alpha spectrometry. This new method can be performed quickly with excellent removal of interferences, high chemical yields and very good alpha peak resolution, eliminating any potential problems with the alpha source preparation for emergency or routine samples. A rapid sequential separation method to separate {sup 210} Po and actinide isotopes was also developed. This new approach, rapid separation with DGA Resin plus microprecipitation for alpha source preparation, is a significant advance in radiochemistry for the rapid

  12. Light

    CERN Document Server

    Ditchburn, R W

    2011-01-01

    This classic study, available for the first time in paperback, clearly demonstrates how quantum theory is a natural development of wave theory, and how these two theories, once thought to be irreconcilable, together comprise a single valid theory of light. Aimed at students with an intermediate-level knowledge of physics, the book first offers a historical introduction to the subject, then covers topics such as wave theory, interference, diffraction, Huygens' Principle, Fermat's Principle, and the accuracy of optical measurements. Additional topics include the velocity of light, relativistic o

  13. $^{206}$ Po sources for production and release studies relevant for high power spallation targets

    CERN Multimedia

    The knowledge of the evaporation behaviour of Po is of essential importance for several scientific and technological applications, like accelerator driven systems (ADS) or the LIEBE project at CERN-ISOLDE. Fundamental investigations on the experimental conditions for the formation of volatile Po species as well as on the chemical composition of the volatile compounds are necessary for a safe operation of such facilities. $^{206}$Po, a mainly $\\gamma$- ray-emitting Po isotope with a half-life of 8.8 d, is best suited for model studies, due to the lower radiation hazard compared to the longer-lived $\\alpha$-emitting isotopes $^{208-210}$Po as well as the easy-to-measure $\\gamma$-ray emission. We propose the production of $^{206}$Po samples in several matrices via the implantation of its precursor $^{210}$Fr into selected metal foils at CERN-ISOLDE. Using these samples, experiments will be carried out at PSI studying the volatilization of Po from different matrices under varying chemical conditions.

  14. Coulomb excitation of neutron-deficient polonium isotopes studied at ISOLDE

    CERN Document Server

    Neven, Michiel

    The polonium isotopes represent an interesting region of the nuclear chart having only two protons outside the Z = 82 closed shell. These isotopes have already been extensively studied theoretically and experimentally. The heavier isotopes (A > 200) seem to follow a "regular seniority-type regime" while for the lighter isotopes (A < 200) a more collective behavior is observed. Many questions remain regarding the transition between these two regimes and the configuration mixing between quantum states. Experiments in the lighter polonium isotopes point to the presence of shape coexistence, however the phenomenon is not fully understood. A Coulomb excitation study of the polonium isotopes whereby the dynamic properties are investigated can provide helpful insights in understanding the shape coexistence phenomena. In this thesis $^{202}$Po was studied via Coulomb excitation. The $^{202}$Po isotope was part of an experimental campaign in which the $^{196,198,200,206}$Po isotopes were studied as well via Coulomb...

  15. BiPO4@Ag3 PO4核/壳异质结的制备及光催化性能%Fabrication and Photocatalytic Activity of BiPO4@Ag3 PO4 Core/Shell Heterojunction

    Institute of Scientific and Technical Information of China (English)

    任延琳; 李新勇; 肇启东

    2014-01-01

    采用简单的水热法结合离子交换法制备了BiPO4@Ag3 PO4核/壳异质结光催化剂,采用场发射扫描电子显微镜(FE-SEM)、透射电子显微镜(TEM)、紫外-可见漫反射光谱仪(DRS)和 X 射线光电子能谱仪(XPS)等对催化剂的形貌、组成、晶型和光物理性质等进行了研究,用罗丹明B(RhB)为模拟水体中有机污染物分别在可见光和模拟太阳光照条件下对催化剂的催化活性进行了测试。结果表明,负载 Ag3 PO4的BiPO4微米棒具有较高的可见光响应,其核/壳异质结结构有利于光生电子-空穴对的有效分离和提高对RhB的光催化降解效率,在可见光和模拟太阳光照射条件下分别在60和40 min可使RhB完全脱色降解。活性物种检测实验结果证明,该催化剂在污染物降解过程中主要的机理是光生空穴的直接氧化。%BiPO4@Ag3 PO4 core/shell heterojuction photocatalyst was synthesized through a facile hydrother-mal process followed by the ion-exchange method. The morphology, crystallinity, composition, and photophy-sical properties of the catalyst were systematically investigated by scanning electron microscope( SEM) , X-ray diffraction(XRD), energy dispersive X-ray analysis, UV-Vis diffuse reflectance spectrophotometer(DRS) and X-ray photoelectron spectroscopy( XPS) . Meanwhile, Rhodamine B( RhB) was chosen as the target pollutant to evaluate the photocatalytic activity of BiPO4@Ag3 PO4 photocatalyst under the visible light and simulated sunlight irradiation, respectively. The results show that RhB was almost totally degraded in 60 min under visi-ble-light irradiation and in 40 min under sunlight irradiation, respectively. The BiPO4@Ag3 PO4 core/shell heterojunction photocatalyst displayed enhanced photocatalytic activity against RhB, which is attributed to the effective charge separation by the core/shell heterojuction between the Ag3 PO4 and BiPO4 . Active species de-tection experiments proved that during

  16. Automatic procedure for mass and charge identification of light isotopes detected in CsI(Tl) of the GARFIELD apparatus

    Energy Technology Data Exchange (ETDEWEB)

    Morelli, L.; Bruno, M.; Baiocco, G. [Dipartimento di Fisica dell' Universita and INFN, Bologna (Italy); Bardelli, L.; Barlini, S.; Bini, M.; Casini, G. [Dipartimento di Fisica dell' Universita and INFN, Firenze (Italy); D' Agostino, M., E-mail: dagostino@bo.infn.i [Dipartimento di Fisica dell' Universita and INFN, Bologna (Italy); Degerlier, M.; Gramegna, F. [INFN, Laboratori Nazionali di Legnaro (Italy); Kravchuk, V.L. [Dipartimento di Fisica dell' Universita and INFN, Bologna (Italy); INFN, Laboratori Nazionali di Legnaro (Italy); Marchi, T. [Dipartimento di Fisica dell' Universita, Padova, ItalyNUCL-EX Collaboration (Italy); INFN, Laboratori Nazionali di Legnaro (Italy); Pasquali, G.; Poggi, G. [Dipartimento di Fisica dell' Universita and INFN, Firenze (Italy)

    2010-08-21

    Mass and charge identification of light charged particles detected with the 180 CsI(Tl) detectors of the GARFIELD apparatus is presented. A 'tracking' method to automatically sample the Z and A ridges of 'Fast-Slow' histograms is developed. An empirical analytic identification function is used to fit correlations between Fast and Slow, in order to determine, event by event, the atomic and mass numbers of the detected charged reaction products. A summary of the advantages of the proposed method with respect to 'hand-based' procedures is reported.

  17. Automatic procedure for mass and charge identification of light isotopes detected in CsI(Tl) of the GARFIELD apparatus

    Science.gov (United States)

    Morelli, L.; Bruno, M.; Baiocco, G.; Bardelli, L.; Barlini, S.; Bini, M.; Casini, G.; D'Agostino, M.; Degerlier, M.; Gramegna, F.; Kravchuk, V. L.; Marchi, T.; Pasquali, G.; Poggi, G.

    2010-08-01

    Mass and charge identification of light charged particles detected with the 180 CsI(Tl) detectors of the GARFIELD apparatus is presented. A "tracking" method to automatically sample the Z and A ridges of "Fast-Slow" histograms is developed. An empirical analytic identification function is used to fit correlations between Fast and Slow, in order to determine, event by event, the atomic and mass numbers of the detected charged reaction products. A summary of the advantages of the proposed method with respect to "hand-based" procedures is reported.

  18. Role of PO4 tetrahedron in LiFePO4 and FePO4 system.

    Science.gov (United States)

    Zeng, Yuewu

    2015-06-01

    Using high resolution transmission electron microscopy with image simulation and Fourier analysis, the Li1- x FePO4 (x LiFePO4 and FePO4 resulting from spinodal decomposition which promote Li ion easily getting into the particle due to uphill diffusion, (3) the particles of FePO4 formed in charging have heavily distorted lattice and contain some isolated LiFePO4 , (4) interface between LiFePO4 and FePO4 and between amorphous and crystal region provides the lattice distortion of small polarons.

  19. Oxygen isotope fractionation in phosphates: the role of dissolved complex anions in isotope exchange.

    Science.gov (United States)

    Zheng, Yong-Fei

    2016-01-01

    Oxygen isotope fractionation factors for phosphates were calculated by means of the increment method. The results suggest that Ag3PO4 and BiPO4 are enriched in (18)O relative to AgPO4, and the three phosphates are consistently depleted in (18)O relative to Ba3[PO4]2; fluorapatite and chlorapatite exhibit a similar behaviour of oxygen isotope fractionation with consistent enrichment of (18)O relative to hydroxyapatite. The valence, radii and coordination of metal cations play a quantitative role in dictating the (18)O/(16)O partitioning in these phosphates of different compositions. The calculated fractionation factors for the Ag3PO4-H2O system are in agreement with experimental determinations derived from enzyme-catalysed isotope exchange between dissolved inorganic phosphate and water at the longest reaction durations at low temperatures. This demonstrates that the precipitated Ag3PO4 has completely captured the oxygen isotope fractionation in the dissolved inorganic phosphate. The calculated fractionation factors for the F/Cl-apatite-water systems are in agreement with the enzyme-catalysed experimental fractionations for the dissolved phosphate-water system at the longest reaction durations but larger than fractionations derived from bacteria-facilitated exchange and inorganic precipitation experiments as well as natural observations. For the experimental calibrations of oxygen isotope fractionation involving the precipitation of dissolved phosphate species from aqueous solutions, the fractionation between precipitate and water is primarily dictated by the isotope equilibration between the dissolved complex anions and water prior to the precipitation. Therefore, the present results provide a quantitative means to interpret the temperature dependence of oxygen isotope fractionation in inorganic and biogenic phosphates.

  20. Inelastic scattering of polarized protons and a possible hexadecapole-shape transition between the light /sup 74,76,78/Se and the heavy /sup 80,82/Se isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Matsuki, S.; Higo, T.; Ohsawa, T.; Shiba, T.; Yanabu, Y.; Ogino, K.; Kadota, Y.; Haga, K.; Sakamoto, N.; Kume, K.; Matoba, M.

    1983-11-07

    The ground-state band up to the 4/sup +/ state in the even /sup 74approximately82/Se isotopes was studied by inelastic scattering of polarized protons at 65 MeV. Both the cross-section sigma(theta) and the analyzing-power A(theta) measurements leading to the 4/sup +/ state in the light /sup 74,76,78/Se isotopes show quite different shapes from those in the heavy /sup 80,82/Se isotopes. Coupled-channels analyses show that both the sigma(theta) and A(theta) distributions are well reproduced with a positive deformation parameter ..beta../sub 4/ in /sup 74,76,78/Se, but with a negative ..beta../sub 4/ in /sup 80,82/Se, indicating a hexadecapole-shape transition between /sup 78/Se and /sup 80/Se.

  1. BiPO{sub 4}/reduced graphene oxide composites photocatalyst with high photocatalytic activity

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Yihe, E-mail: zyh@cugb.edu.cn [National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences, Beijing 10083 (China); Shen, Bo [National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences, Beijing 10083 (China); Huang, Hongwei, E-mail: hhw@cugb.edu.cn [National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences, Beijing 10083 (China); He, Ying [National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences, Beijing 10083 (China); Fei, Bin [Institute of Textile and Clothing, The Hong Kong Polytechnic University, Kowloon, Hong Kong (China); Lv, Fengzhu [National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences, Beijing 10083 (China)

    2014-11-15

    Graphical abstract: The composite photocatalysts composed of BiPO{sub 4} and reduced graphene oxide (rGO) were synthesized by a facile hydrothermal method. The BiPO{sub 4}/rGO composites exhibit much better photocatalytic performance than pure BiPO{sub 4}. - Highlights: • BiPO{sub 4} nanoparticles are immobilized on reduced graphene oxide (rGO) as photocatalysts. • The BiPO{sub 4}/rGO composites show enhanced photocatalytic activity than the pure BiPO{sub 4} nanoparticles. • The crystallization phases of BiPO{sub 4} can be determined by the amount of graphene. - Abstract: The composite photocatalysts composed of BiPO{sub 4} and reduced graphene oxide (rGO) were synthesized by a facile hydrothermal method. Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), transmission electron spectroscopy (TEM), photoluminescence emission spectra (PL) and UV–vis diffuse reflection spectroscopy (DRS) were used to characterize the titled composites. The results showed that the BiPO{sub 4} particles can be immobilized on the surface of rGO sheets, and the crystallization phases of BiPO{sub 4} were significantly influenced by the amount of graphene. The phase transformation of BiPO{sub 4} crystal from hexagonal to monoclinic phase was observed. The introduction of rGO improved the optical properties of BiPO{sub 4} and thereby enhancing the utilization of light. Compared with pure BiPO{sub 4} under similar synthesis condition, the BiPO{sub 4}/rGO composites exhibit a much higher photodegradation activity, which was confirmed by photoluminescence (PL) spectra and photocurrent (PC) generation.

  2. Natural levels of {sup 210}Po in human urine

    Energy Technology Data Exchange (ETDEWEB)

    Diaz-Frances, I.; Manjon, G.; Mantero, J.; Diaz, J. [Departament of Applied Phisic II, University of Seville, P.O. Box 41012 Seville (Spain); Garcia-Tenorio, R. [Departament of Applied Phisic II, University of Seville, P.O. Box 41012 Seville (Spain); National Accelerator Centre, P.O. Box 41092 Seville (Spain)

    2014-07-01

    Since the secret agent Alexander Litvinenko was murdered in 2006 by a {sup 210}Po lethal dose, presumably ingested, there is renovated interest on the toxicity of this radionuclide in humans. {sup 210}Po is a radioactive isotope naturally found in nature, mainly incorporated by humans via food and water ingestion, as well as inhaled through its progenitor, the {sup 222}Rn. The total amount of natural {sup 210}Po in the human body can vary from person to person depending on their lifestyle: dietary habits, drinking water source, place of residence (associated with exposure to {sup 222}Rn), etc- and therefore in the concentrations of this element to be found in urine. To analyze the influence of dietary habits on the amount of {sup 210}Po excreted in urine, two volunteers in Seville had a well-defined and time-varying diet for a month, following a daily collection of their urine and determination of the concentrations therein of this radionuclide. The results obtained and the conclusions derived from them form the core of this communication. {sup 210}Po determinations were performed daily in 200 ml aliquots of urine using the technique of high resolution alpha spectrometry. This has involved the application of a single radiochemical method for the concentration and isolation {sup 210}Po, followed by its auto-deposition on copper planchets for proper measure. Daily {sup 210}Po activity concentrations in voluntary urine analyzed during the month of study show high variability with a difference of up to an order of magnitude between maximum and minimum values obtained, and a clear dependence on the diet type followed in the various stages of the experiment. The lowest concentrations obtained are associated with a diet rich in carbohydrates and proteins 'terrestrial' (pork, beef,...), while the highest concentrations were obtained in the final phase of the experiment when the diet was enriched with presence of marine products in fair correspondence with the

  3. RbYb(PO34

    Directory of Open Access Journals (Sweden)

    Hui Chen

    2013-01-01

    Full Text Available Rubidium ytterbium(III tetrakis(polyphosphate, RbYb(PO34, was synthesized by solid-state reaction. It adopts structure type IV of the MRE(PO34 (M = alkali metal and RE = rare earth metal family of compounds. The structure is composed of a three-dimensional framework made up from double spiral polyphosphate chains parallel to [10-1] and irregular [YbO8] polyhedra. There are eight PO4 tetrahedra in the repeat unit of the polyphosphate chains. The Rb+ cation is located in channels extending along [100] that are delimited by the three-dimensional framework. It is surrounded by 11 O atoms, defining an irregular polyhedron.

  4. LiDy(PO34

    Directory of Open Access Journals (Sweden)

    Fathia Chehimi-Moumen

    2008-07-01

    Full Text Available Single crystals of lithium dysprosium polyphosphate, LiDy(PO34, were prepared by the flux method. The atomic arrangement is built up by infinite (PO3n chains extending along the b axis. Dy3+ and Li+ cations alternate in the middle of four such chains, with Dy...Li distances of 3.54 (1 and 3.48 (1 Å. The DyO8 dodecahedra and LiO4 tetrahedra deviate significantly from the ideal geometry. Both Dy and Li occupy special positions (Wyckoff position 4e, site symmetry 2.

  5. Alpha-Decay of $^{211}Po$ on the 1633 keV $^{207}Pb$ level

    CERN Document Server

    Chumin, V G; Malikov, Sh R; Norseev, Yu V; Samatov, Z K; Fominykh, V I; Cherevatenko, A P; Yurkova, L V

    2000-01-01

    In investigations of gamma-spectrum of ^{211}At and daughter ^{211}Po and ^{207}Bi isotopes a new branch of the alpha-decay on the ^{207}Pb 1633 keV level is discovered. Its intensity is 8.1 cdot 10^{-4} %.

  6. Oxygen isotope studies of phosphite oxidation: purification and analysis of reactants and products by high-temperature conversion elemental analyzer/isotope ratio mass spectrometry.

    Science.gov (United States)

    Chang, Sae Jung; Blake, Ruth E

    2015-11-15

    Increased attention has been recently focused on the origin and reactions of reduced-P oxyanions such as phosphite [PO3 (III)] in terrestrial and biological systems. We present new methods for studying O-isotopic reactions between PO3 (III) and other oxygen sources during oxidation of PO3 (III) to PO4 (V). Na2 (HPO3 )·5H2 O, used as a PO3 (III) source, contains structural water due to its hygroscopic nature; thus, we developed a method for determining the δ(18) O value of PO3 (III) after the removal of structural water. Next, we tested two techniques for purifying PO4 (V) from aqueous PO3 (III)/PO4 (V) mixtures: (1) precipitation of PO4 (V) as ammonium phosphomolybdate (APM); and (2) precipitation of PO4 (V) as magnesium ammonium phosphate (MAP). The O-isotope compositions, (18) O:(16) O (δ(18) O values), of Na2 (HPO3 ) and Ag3 PO4 were analyzed by TC/EA/IRMS. Structural water was removed from Na2 (HPO3 )·5H2 O after drying at 100 °C under vacuum and the δ(18) O value of PO3 (III) was obtained. The δ(18) O values of PO4 (V), which was extracted from (18) O-labeled PO3 (III)/PO4 (V) mixtures by APM and MAP precipitations, were not altered by the precipitation process. This result confirms that PO3 (III) is not converted into PO4 (V) by oxidation or hydrolysis under either strong acidic/oxidizing (APM) or alkaline (MAP) conditions for up to a 24-h period. We conclude that both APM and MAP precipitation are reliable and effective methods for the separation and purification of PO4 (V) from aqueous PO3 (III)/PO4 (V) mixtures. The methods described here will permit the study of the isotopic evolution of various pathways of geochemical as well as biological PO3 (III) oxidation. Copyright © 2015 John Wiley & Sons, Ltd.

  7. CsMgPO4

    Directory of Open Access Journals (Sweden)

    Nikolay S. Slobodyanik

    2009-08-01

    Full Text Available Caesium magnesium orthophosphate is built up from MgO4 and PO4 tetrahedra (both with . m. symmetry linked together by corners, forming a three-dimensional framework. The Cs atoms have .m. site symmetry and are located in hexagonal channels running along the a- and b-axis directions.

  8. Atomic Mass and Nuclear Binding Energy for Po-269 (Polonium)

    Science.gov (United States)

    Sukhoruchkin, S. I.; Soroko, Z. N.

    This document is part of the Supplement containing the complete sets of data of Subvolume B `Nuclei with Z = 55 - 100' of Volume 22 `Nuclear Binding Energies and Atomic Masses' of Landolt-Börnstein - Group I `Elementary Particles, Nuclei and Atoms', and additionally including data for nuclei with Z = 101 - 130. It provides atomic mass, mass excess, nuclear binding energy, nucleon separation energies, Q-values, and nucleon residual interaction parameters for atomic nuclei of the isotope Po-269 (Polonium, atomic number Z = 84, mass number A = 269).

  9. Atomic Mass and Nuclear Binding Energy for Po-278 (Polonium)

    Science.gov (United States)

    Sukhoruchkin, S. I.; Soroko, Z. N.

    This document is part of the Supplement containing the complete sets of data of Subvolume B `Nuclei with Z = 55 - 100' of Volume 22 `Nuclear Binding Energies and Atomic Masses' of Landolt-Börnstein - Group I `Elementary Particles, Nuclei and Atoms', and additionally including data for nuclei with Z = 101 - 130. It provides atomic mass, mass excess, nuclear binding energy, nucleon separation energies, Q-values, and nucleon residual interaction parameters for atomic nuclei of the isotope Po-278 (Polonium, atomic number Z = 84, mass number A = 278).

  10. Atomic Mass and Nuclear Binding Energy for Po-282 (Polonium)

    Science.gov (United States)

    Sukhoruchkin, S. I.; Soroko, Z. N.

    This document is part of the Supplement containing the complete sets of data of Subvolume B `Nuclei with Z = 55 - 100' of Volume 22 `Nuclear Binding Energies and Atomic Masses' of Landolt-Börnstein - Group I `Elementary Particles, Nuclei and Atoms', and additionally including data for nuclei with Z = 101 - 130. It provides atomic mass, mass excess, nuclear binding energy, nucleon separation energies, Q-values, and nucleon residual interaction parameters for atomic nuclei of the isotope Po-282 (Polonium, atomic number Z = 84, mass number A = 282).

  11. Atomic Mass and Nuclear Binding Energy for Po-271 (Polonium)

    Science.gov (United States)

    Sukhoruchkin, S. I.; Soroko, Z. N.

    This document is part of the Supplement containing the complete sets of data of Subvolume B `Nuclei with Z = 55 - 100' of Volume 22 `Nuclear Binding Energies and Atomic Masses' of Landolt-Börnstein - Group I `Elementary Particles, Nuclei and Atoms', and additionally including data for nuclei with Z = 101 - 130. It provides atomic mass, mass excess, nuclear binding energy, nucleon separation energies, Q-values, and nucleon residual interaction parameters for atomic nuclei of the isotope Po-271 (Polonium, atomic number Z = 84, mass number A = 271).

  12. Atomic Mass and Nuclear Binding Energy for Po-283 (Polonium)

    Science.gov (United States)

    Sukhoruchkin, S. I.; Soroko, Z. N.

    This document is part of the Supplement containing the complete sets of data of Subvolume B `Nuclei with Z = 55 - 100' of Volume 22 `Nuclear Binding Energies and Atomic Masses' of Landolt-Börnstein - Group I `Elementary Particles, Nuclei and Atoms', and additionally including data for nuclei with Z = 101 - 130. It provides atomic mass, mass excess, nuclear binding energy, nucleon separation energies, Q-values, and nucleon residual interaction parameters for atomic nuclei of the isotope Po-283 (Polonium, atomic number Z = 84, mass number A = 283).

  13. Atomic Mass and Nuclear Binding Energy for Po-281 (Polonium)

    Science.gov (United States)

    Sukhoruchkin, S. I.; Soroko, Z. N.

    This document is part of the Supplement containing the complete sets of data of Subvolume B `Nuclei with Z = 55 - 100' of Volume 22 `Nuclear Binding Energies and Atomic Masses' of Landolt-Börnstein - Group I `Elementary Particles, Nuclei and Atoms', and additionally including data for nuclei with Z = 101 - 130. It provides atomic mass, mass excess, nuclear binding energy, nucleon separation energies, Q-values, and nucleon residual interaction parameters for atomic nuclei of the isotope Po-281 (Polonium, atomic number Z = 84, mass number A = 281).

  14. Atomic Mass and Nuclear Binding Energy for Po-284 (Polonium)

    Science.gov (United States)

    Sukhoruchkin, S. I.; Soroko, Z. N.

    This document is part of the Supplement containing the complete sets of data of Subvolume B `Nuclei with Z = 55 - 100' of Volume 22 `Nuclear Binding Energies and Atomic Masses' of Landolt-Börnstein - Group I `Elementary Particles, Nuclei and Atoms', and additionally including data for nuclei with Z = 101 - 130. It provides atomic mass, mass excess, nuclear binding energy, nucleon separation energies, Q-values, and nucleon residual interaction parameters for atomic nuclei of the isotope Po-284 (Polonium, atomic number Z = 84, mass number A = 284).

  15. Atomic Mass and Nuclear Binding Energy for Po-280 (Polonium)

    Science.gov (United States)

    Sukhoruchkin, S. I.; Soroko, Z. N.

    This document is part of the Supplement containing the complete sets of data of Subvolume B `Nuclei with Z = 55 - 100' of Volume 22 `Nuclear Binding Energies and Atomic Masses' of Landolt-Börnstein - Group I `Elementary Particles, Nuclei and Atoms', and additionally including data for nuclei with Z = 101 - 130. It provides atomic mass, mass excess, nuclear binding energy, nucleon separation energies, Q-values, and nucleon residual interaction parameters for atomic nuclei of the isotope Po-280 (Polonium, atomic number Z = 84, mass number A = 280).

  16. Atomic Mass and Nuclear Binding Energy for Po-272 (Polonium)

    Science.gov (United States)

    Sukhoruchkin, S. I.; Soroko, Z. N.

    This document is part of the Supplement containing the complete sets of data of Subvolume B `Nuclei with Z = 55 - 100' of Volume 22 `Nuclear Binding Energies and Atomic Masses' of Landolt-Börnstein - Group I `Elementary Particles, Nuclei and Atoms', and additionally including data for nuclei with Z = 101 - 130. It provides atomic mass, mass excess, nuclear binding energy, nucleon separation energies, Q-values, and nucleon residual interaction parameters for atomic nuclei of the isotope Po-272 (Polonium, atomic number Z = 84, mass number A = 272).

  17. Atomic Mass and Nuclear Binding Energy for Po-276 (Polonium)

    Science.gov (United States)

    Sukhoruchkin, S. I.; Soroko, Z. N.

    This document is part of the Supplement containing the complete sets of data of Subvolume B `Nuclei with Z = 55 - 100' of Volume 22 `Nuclear Binding Energies and Atomic Masses' of Landolt-Börnstein - Group I `Elementary Particles, Nuclei and Atoms', and additionally including data for nuclei with Z = 101 - 130. It provides atomic mass, mass excess, nuclear binding energy, nucleon separation energies, Q-values, and nucleon residual interaction parameters for atomic nuclei of the isotope Po-276 (Polonium, atomic number Z = 84, mass number A = 276).

  18. Atomic Mass and Nuclear Binding Energy for Po-277 (Polonium)

    Science.gov (United States)

    Sukhoruchkin, S. I.; Soroko, Z. N.

    This document is part of the Supplement containing the complete sets of data of Subvolume B `Nuclei with Z = 55 - 100' of Volume 22 `Nuclear Binding Energies and Atomic Masses' of Landolt-Börnstein - Group I `Elementary Particles, Nuclei and Atoms', and additionally including data for nuclei with Z = 101 - 130. It provides atomic mass, mass excess, nuclear binding energy, nucleon separation energies, Q-values, and nucleon residual interaction parameters for atomic nuclei of the isotope Po-277 (Polonium, atomic number Z = 84, mass number A = 277).

  19. Atomic Mass and Nuclear Binding Energy for Po-275 (Polonium)

    Science.gov (United States)

    Sukhoruchkin, S. I.; Soroko, Z. N.

    This document is part of the Supplement containing the complete sets of data of Subvolume B `Nuclei with Z = 55 - 100' of Volume 22 `Nuclear Binding Energies and Atomic Masses' of Landolt-Börnstein - Group I `Elementary Particles, Nuclei and Atoms', and additionally including data for nuclei with Z = 101 - 130. It provides atomic mass, mass excess, nuclear binding energy, nucleon separation energies, Q-values, and nucleon residual interaction parameters for atomic nuclei of the isotope Po-275 (Polonium, atomic number Z = 84, mass number A = 275).

  20. Atomic Mass and Nuclear Binding Energy for Po-273 (Polonium)

    Science.gov (United States)

    Sukhoruchkin, S. I.; Soroko, Z. N.

    This document is part of the Supplement containing the complete sets of data of Subvolume B `Nuclei with Z = 55 - 100' of Volume 22 `Nuclear Binding Energies and Atomic Masses' of Landolt-Börnstein - Group I `Elementary Particles, Nuclei and Atoms', and additionally including data for nuclei with Z = 101 - 130. It provides atomic mass, mass excess, nuclear binding energy, nucleon separation energies, Q-values, and nucleon residual interaction parameters for atomic nuclei of the isotope Po-273 (Polonium, atomic number Z = 84, mass number A = 273).

  1. Atomic Mass and Nuclear Binding Energy for Po-274 (Polonium)

    Science.gov (United States)

    Sukhoruchkin, S. I.; Soroko, Z. N.

    This document is part of the Supplement containing the complete sets of data of Subvolume B `Nuclei with Z = 55 - 100' of Volume 22 `Nuclear Binding Energies and Atomic Masses' of Landolt-Börnstein - Group I `Elementary Particles, Nuclei and Atoms', and additionally including data for nuclei with Z = 101 - 130. It provides atomic mass, mass excess, nuclear binding energy, nucleon separation energies, Q-values, and nucleon residual interaction parameters for atomic nuclei of the isotope Po-274 (Polonium, atomic number Z = 84, mass number A = 274).

  2. Atomic Mass and Nuclear Binding Energy for Po-270 (Polonium)

    Science.gov (United States)

    Sukhoruchkin, S. I.; Soroko, Z. N.

    This document is part of the Supplement containing the complete sets of data of Subvolume B `Nuclei with Z = 55 - 100' of Volume 22 `Nuclear Binding Energies and Atomic Masses' of Landolt-Börnstein - Group I `Elementary Particles, Nuclei and Atoms', and additionally including data for nuclei with Z = 101 - 130. It provides atomic mass, mass excess, nuclear binding energy, nucleon separation energies, Q-values, and nucleon residual interaction parameters for atomic nuclei of the isotope Po-270 (Polonium, atomic number Z = 84, mass number A = 270).

  3. Atomic Mass and Nuclear Binding Energy for Po-279 (Polonium)

    Science.gov (United States)

    Sukhoruchkin, S. I.; Soroko, Z. N.

    This document is part of the Supplement containing the complete sets of data of Subvolume B `Nuclei with Z = 55 - 100' of Volume 22 `Nuclear Binding Energies and Atomic Masses' of Landolt-Börnstein - Group I `Elementary Particles, Nuclei and Atoms', and additionally including data for nuclei with Z = 101 - 130. It provides atomic mass, mass excess, nuclear binding energy, nucleon separation energies, Q-values, and nucleon residual interaction parameters for atomic nuclei of the isotope Po-279 (Polonium, atomic number Z = 84, mass number A = 279).

  4. Origin of Activity and Stability Enhancement for Ag3PO4 Photocatalyst after Calcination

    Directory of Open Access Journals (Sweden)

    Pengyu Dong

    2016-11-01

    Full Text Available Pristine Ag3PO4 microspheres were synthesized by a co-precipitation method, followed by being calcined at different temperatures to obtain a series of calcined Ag3PO4 photocatalysts. This work aims to investigate the origin of activity and stability enhancement for Ag3PO4 photocatalyst after calcination based on the systematical analyses of the structures, morphologies, chemical states of elements, oxygen defects, optical absorption properties, separation and transfer of photogenerated electron-hole pairs, and active species. The results indicate that oxygen vacancies (VO˙˙ are created and metallic silver nanoparticles (Ag NPs are formed by the reaction of partial Ag+ in Ag3PO4 semiconductor with the thermally excited electrons from Ag3PO4 and then deposited on the surface of Ag3PO4 microspheres during the calcination process. Among the calcined Ag3PO4 samples, the Ag3PO4-200 sample exhibits the best photocatalytic activity and greatly enhanced photocatalytic stability for photodegradation of methylene blue (MB solution under visible light irradiation. Oxygen vacancies play a significantly positive role in the enhancement of photocatalytic activity, while metallic Ag has a very important effect on improving the photocatalytic stability. Overall, the present work provides some powerful evidences and a deep understanding on the origin of activity and stability enhancement for the Ag3PO4 photocatalyst after calcination.

  5. Tooth enamel maturation reequilibrates oxygen isotope compositions and supports simple sampling methods

    Science.gov (United States)

    Trayler, Robin B.; Kohn, Matthew J.

    2017-02-01

    Oxygen isotope and major element zoning patterns of several disparate ungulate teeth were collected to evaluate the timing and geometry of enamel formation, records of isotope zoning, and tooth enamel sampling strategies. Isotopic zoning in mammalian tooth enamel encodes a sub-annual time series of isotopic variation of an animal's body water composition, with a damping factor that depends on the specifics of how enamel mineralizes. Enamel formation comprises two stages: precipitation of appositional enamel with a high CO3:PO4 ratio, followed by precipitation of maturational enamel with a lower CO3:PO4. If appositional and maturational enamel both contribute to isotope compositions (but with different CO3:PO4), and if isotope compositions vary seasonally, paired δ18O values from CO3 and PO4 profiles should show a spatial separation. CO3 isotope patterns should be shifted earlier seasonally than PO4 isotope patterns. Such paired profiles for new and published data show no resolvable shifts, i.e. CO3 and PO4 δ18O profiles show coincident maxima and minima. This coincidence suggests that enamel maturation reequilibrates appositional isotope compositions. If enamel maturation establishes enamel isotope compositions, the geometry of maturation, not apposition, should be considered when devising sampling protocols. X-ray maps of Ca zoning show that the majority of enamel (inner and middle layers) mineralizes heavily at a high angle to the external tooth surface and the enamel-dentine junction over length scales of 2-4 mm, while the outer enamel surface mineralizes more slowly. These data suggest that isotopic sampling strategies should parallel maturational geometry and focus on interior enamel to improve data fidelity. The magnitude of isotopic damping is also smaller than implied in previous studies, so tooth enamel zoning more closely reflects original body water isotopic variations than previously assumed.

  6. Development of a simplified methodology for the isotopic determination of fuel spent in Light Water Reactors; Desarrollo de una metodologia simplificada para la determinacion isotopica del combustible gastado en reactores de agua ligera

    Energy Technology Data Exchange (ETDEWEB)

    Hernandez N, H.; Francois L, J.L. [FI-UNAM, 04510 Mexico D.F. (Mexico)]. e-mail: hermilo@lairn.fi-b.unam.mx

    2005-07-01

    The present work presents a simplified methodology to quantify the isotopic content of the spent fuel of light water reactors; their application is it specific to the Laguna Verde Nucleo electric Central by means of a balance cycle of 18 months. The methodology is divided in two parts: the first one consists on the development of a model of a simplified cell, for the isotopic quantification of the irradiated fuel. With this model the burnt one is simulated 48,000 MWD/TU of the fuel in the core of the reactor, taking like base one fuel assemble type 10x10 and using a two-dimensional simulator for a fuel cell of a light water reactor (CPM-3). The second part of the methodology is based on the creation from an isotopic decay model through an algorithm in C++ (decay) to evaluate the amount, by decay of the radionuclides, after having been irradiated the fuel until the time in which the reprocessing is made. Finally the method used for the quantification of the kilograms of uranium and obtained plutonium of a normalized quantity (1000 kg) of fuel irradiated in a reactor is presented. These results will allow later on to make analysis of the final disposition of the irradiated fuel. (Author)

  7. Poésie et politique

    OpenAIRE

    Artières,Philippe; Avanza, Martina; Baranova, Tatiana Debbagi; Belalimat, Nadia; Bourdin, Alain; Callac, Emmanuelle; Clément, Fabrice; Čolović, Ivan; Dragomir, Lucia; Huhn, Rosemarie; Martel, Philippe; Morel, Alain

    2005-01-01

    Qu'il s'agisse de poésie officielle, révolutionnaire, protestataire ou partisane ou encore du rôle des poètes dans la vie quotidienne de la cité, ce sont les usages sociaux et politiques de la poésie aujourd'hui sont au centre de ce dossier.

  8. Tunable-color luminescence via energy transfer in NaCa13/18Mg5/18PO4:A (A = Eu2+/Tb3+/Mn2+, Dy3+) phosphors for solid state lighting.

    Science.gov (United States)

    Li, Kai; Fan, Jian; Mi, Xiaoyun; Zhang, Yang; Lian, Hongzhou; Shang, Mengmeng; Lin, Jun

    2014-11-17

    A series of NaCa13/18Mg5/18PO4(NCMPO):A (A = Eu(2+)/Tb(3+)/Mn(2+), Dy(3+)) phosphors have been prepared by the high-temperature solid-state reaction method. The X-ray diffraction (XRD) and Rietveld refinement, X-ray photoelectron spectroscopy (XPS), photoluminescence (PL), cathodoluminescence (CL), decay lifetimes, and PL quantum yields (QYs) were utilized to characterize the phosphors. The pure crystalline phase of as-prepared samples has been demonstrated via XRD measurement and Rietveld refinements. XPS reveals that the Eu(2+)/Tb(3+)/Mn(2+) can be efficiently doped into the crystal lattice. NCMPO:Eu(2+)/Tb(3+)/Mn(2+) phosphors can be effectively excited under UV radiation, which show tunable color from purple-blue to red including white emission based on energy transfer from Eu(2+) to Tb(3+)/Mn(2+) ions. Under low-voltage electron beam bombardment, the NCMPO:A (A = Eu(2+)/Tb(3+)/Mn(2+), Dy(3+)) display their, respectively, characteristic emissions with different colors, and the CL spectrum of NCMPO:0.04Tb(3+) has the comparable intensity to the ZnO:Zn commercial product. In addition, the calculated CIE coordinate of NCMPO:0.04Tb(3+) (0.252, 0.432) is more saturated than it (0.195, 0.417). These results reveal that NCMPO:A (A = Eu(2+)/Tb(3+)/Mn(2+), Dy(3+)) may be potential candidate phosphors for WLEDs and FEDs.

  9. Synthesis and Photocatalytic Activity of Ag3PO4 Triangular Prism

    Directory of Open Access Journals (Sweden)

    Pengyu Dong

    2015-01-01

    Full Text Available Ag3PO4 triangular prism was synthesized by a facile chemical precipitation approach by simply adjusting external ultrasonic condition. The as-synthesized Ag3PO4 triangular prism was characterized by X-ray diffraction pattern (XRD, field emission scanning electron microscopy (SEM, fourier transform infrared (FTIR spectra, and ultraviolet-visible diffuse reflectance (UV-vis DRS absorption spectra. The photocatalytic activity of Ag3PO4 triangular prism was evaluated by photodegradation of organic methylene blue (MB, rhodamine B (RhB, and phenol under visible light irradiation. Results showed that Ag3PO4 triangular prism exhibited higher photocatalytic activity than N-doped TiO2 and commercial TiO2 (P25 under visible light irradiation.

  10. Stable carbon isotopes of C3 plant resins and ambers record changes in atmospheric oxygen since the Triassic

    Science.gov (United States)

    Tappert, Ralf; McKellar, Ryan C.; Wolfe, Alexander P.; Tappert, Michelle C.; Ortega-Blanco, Jaime; Muehlenbachs, Karlis

    2013-11-01

    Estimating the partial pressure of atmospheric oxygen (pO2) in the geological past has been challenging because of the lack of reliable proxies. Here we develop a technique to estimate paleo-pO2 using the stable carbon isotope composition (δ13C) of plant resins-including amber, copal, and resinite-from a wide range of localities and ages (Triassic to modern). Plant resins are particularly suitable as proxies because their highly cross-linked terpenoid structures allow the preservation of pristine δ13C signatures over geological timescales. The distribution of δ13C values of modern resins (n = 126) indicates that (a) resin-producing plant families generally have a similar fractionation behavior during resin biosynthesis, and (b) the fractionation observed in resins is similar to that of bulk plant matter. Resins exhibit a natural variability in δ13C of around 8‰ (δ13C range: -31‰ to -23‰, mean: -27‰), which is caused by local environmental and ecological factors (e.g., water availability, water composition, light exposure, temperature, nutrient availability). To minimize the effects of local conditions and to determine long-term changes in the δ13C of resins, we used mean δ13C values (δ13Cmeanresin) for each geological resin deposit. Fossil resins (n = 412) are generally enriched in 13C compared to their modern counterparts, with shifts in δ13Cmeanresin of up to 6‰. These isotopic shifts follow distinctive trends through time, which are unrelated to post-depositional processes including polymerization and diagenesis. The most enriched fossil resin samples, with a δ13Cmeanresin between -22‰ and -21‰, formed during the Triassic, the mid-Cretaceous, and the early Eocene. Experimental evidence and theoretical considerations suggest that neither change in pCO2 nor in the δ13C of atmospheric CO2 can account for the observed shifts in δ13Cmeanresin. The fractionation of 13C in resin-producing plants (Δ13C), instead, is primarily influenced by

  11. Požarna varnost lesenih konstrukcij

    OpenAIRE

    Štupnik, Igor

    2016-01-01

    Namen diplomske naloge je prikaz postopkov izračuna požarne varnosti lesenih konstrukcij. Predstavljeni so predlogi izboljšave izračunov po standardu SIST EN 1995-1-2, ki temeljijo na požarnih testih in so opisani v Evropskih tehničnih smernicah. Praktični izračuni so prikazani na primerih lesenih elementov Vrtca Preddvor.

  12. Solvothermal synthesis of Ag hybrid BiPO4 heterostructures with enhanced photodegradation activity and stability.

    Science.gov (United States)

    Huang, Chang-Wei; Wu, Mei-Yao; Lin, Yang-Wei

    2017-03-15

    In this study, Ag hybrid BiPO4 (Ag/BiPO4) heterostructures were synthesized using a solvothermal method. The morphologies and optical properties of the Ag/BiPO4 heterostructures were drastically different from those of BiPO4 and were highly dependent on the AgNO3:BiPO4 weight percent during the synthesis. The three formulated heterostructures were evaluated for their photocatalytic degradation of methylene blue (MB) under UV light illumination; the 0.5%Ag/BiPO4 heterostructure was observed to result in 99% degradation of MB within 60min, a remarkably higher level of photodegradation activity than the levels caused by TiO2 and BiPO4. Furthermore, even after use for five cycles of MB degradation, the 0.5%Ag/BiPO4 heterostructure showed no observable loss in photodegradation activity and no change in XRD patterns, demonstrating its chemical and structural stability. According to the results of a systematic experimental investigation, the enhanced photodegradation activity of this Ag/BiPO4 heterostructure could be ascribed to the high position of its valence band and the highly efficient separation of photogenerated electrons and holes. Moreover, hydroxyl radicals and holes were found to be the major reactive species. Successful photodegradation of standard dye solutions, including acid blue 1, methyl orange, fast green, rhodamine B, rhodamine 6G, and MB, in real water samples was demonstrated with the 0.5%Ag/BiPO4 heterostructure, providing clear evidence of its utility for treating waste water containing organic dyes.

  13. Stability of luminescence in LaPO4, LaPO4 :RE(3+) (RE = Dy, Eu) nanophosphors.

    Science.gov (United States)

    Pimpalshende, D M; Dhoble, S J

    2015-03-01

    The property of high refractive index, low solubility in water as well as stability to high temperature variation of lanthanum phosphate (LaPO4 ) proved it was the most effective candidate for the production of display lamps, and plasma display panel devices and sensors. The morphological and nanostructural characteristics play a key role in the working efficiency of the luminescent material. These properties can be controlled by the synthesis method, which we have adopted in this paper. We have prepared LaPO4 nanoparticles at a relatively low temperature (110 ºC) in polyethylene glycol medium by using a wet chemical one-step synthesis. The phase composition and structural properties of the sample have been characterized by X-ray diffraction, Fourier transform infrared, transmission electron microscopy and the luminescent property by photoluminescence and thermoluminescence. The samples were well crystallized and the average crystallite size of 15 nm has been calculated for pure LaPO4 using the Debye-Scherrer equation. The result from heat-treated samples shows the phase combination and morphological structure of the powder depend on the annealing temperature. The heat treatment changes the structure of LaPO4 from cuboid rods to fine grains at about 600 °C. The emission spectrum of LaPO4 shows the broad emission band at 368 nm and shoulder at 465 nm with emission of blue color when monitored at an excitation wavelength at 256 nm. The stability of phosphor has been studied with respect to humidity, temperature, doping, doping concentration, γ-ray exposures, etc. The prepared nanosized phosphors were thermally stable and may be a promising blue phosphor for lighting technology as well as radiation dosimetry.

  14. The spectroscopic studies of glasses in the BPO 4(GaPO 4)-SiO 2 system

    Science.gov (United States)

    Adamczyk, A.

    2002-09-01

    FTIR spectroscopic structural studies of gel-derived glasses in BPO 4-SiO 2 and BPO 4(GaPO 4)-SiO 2 systems are presented. 10B isotope substitution, spectra subtraction procedure and B 3+→Ga 3+ substitution were applied to distinguish the bands, originating from B-O, P-O and Si-O bond vibrations. The spectra of borophosphosilicate glasses containing 10B isotope have also been presented. Changes in the band positions helped to assign bands due to the different B-O bonds vibrations. The spectra subtraction procedure, due to the lowering of intensity of bands assigned to Si-O bonds vibrations, enabled to observe bands at 966 and 1225 cm -1, due to broken Si-O - bridges and (PO 2) - terminal groups, respectively.

  15. Copper isotope signatures in modern marine sediments

    Science.gov (United States)

    Little, Susan H.; Vance, Derek; McManus, James; Severmann, Silke; Lyons, Timothy W.

    2017-09-01

    The development of metal stable isotopes as tools in paleoceanography requires a thorough understanding of their modern marine cycling. To date, no Cu isotope data has been published for modern sediments deposited under low oxygen conditions. We present data encompassing a broad spectrum of hydrographic and redox regimes, including continental margin and euxinic (sulphide-containing) settings. Taken together with previously published data from oxic settings, these data indicate that the modern oceanic sink for Cu has a surprisingly homogeneous isotopic composition of about +0.3‰ (δ65Cu, relative to NIST SRM976). We suggest that this signature reflects one of two specific water-column processes: (1) an equilibrium isotope fractionation between soluble, isotopically heavy, Cu complexed to strong organic ligands and an isotopically light pool sorbed to particles that deliver Cu to the sediment, or (2) an equilibrium isotope fractionation between the same isotopically heavy ligand-bound pool and the particle reactive free Cu2+ species, with the latter being scavenged by particulates and thereby delivered to the sediment. An output flux of about +0.3‰ into sediments is isotopically light relative to the known inputs to the ocean (at around +0.6‰) and the seawater value of +0.6 to +0.9‰, suggesting the presence of an as yet unidentified isotopically light source of Cu to the oceans. We hypothesize that this source may be hydrothermal, or may result from the partial dissolution of continentally derived particles.

  16. Biogeochemical factors affecting the presence of {sup 210}Po in groundwater

    Energy Technology Data Exchange (ETDEWEB)

    Seiler, Ralph L., E-mail: rseiler@usgs.gov [US Geological Survey, Nevada Water Science Center, 2730 N. Deer Run Road, Carson City, NV 89701 (United States); Stillings, Lisa L. [US Geological Survey, MacKay School of Mines, MS-176, University of Nevada Reno, Reno, NV 89557 (United States); Cutler, Nichole [Hydrologic Sciences Graduate Program, MS-176, University of Nevada Reno, Reno, NV 89557 (United States); Salonen, Laina; Outola, Iisa [STUK, Radiation and Nuclear Safety Authority, P.O. Box 14, FIN-00881 Helsinki (Finland)

    2011-04-15

    Research highlights: {yields} {sup 210}Po activities in numerous domestic wells in Fallon NV exceed 500 mBq/L. {yields} {sup 210}Po levels in sediment are not the primary determinant on levels in groundwater. {yields} {delta}{sup 34}S measurements indicate SO{sub 4} reduction occurred in all {sup 210}Po contaminated wells. {yields} {sup 210}Po contaminated wells are anoxic, have high pH and low Ca. {yields} Po mobilization probably involves an anaerobic S cycle in which H{sub 2}S dissolves MnO{sub 2}. - Abstract: The discovery of natural {sup 210}Po enrichment at levels exceeding 500 mBq/L in numerous domestic wells in northern Nevada, USA, led to a geochemical investigation of the processes responsible for its mobilization. {sup 210}Po activities in 63 domestic and public-supply wells ranged from below 1 mBq/L to 6590 {+-} 590 mBq/L, among the highest reported levels in the USA. There is little spatial or depth variability in {sup 210}Pb activity in study-area sediments and mobilization of a few percent of the {sup 210}Po in the sediments would account for all of the {sup 210}Po in water. Stable-isotope measurements indicate SO{sub 4} reduction has occurred in all {sup 210}Po contaminated wells. Sulfide species are not accumulating in the groundwater in much of Lahontan Valley, probably because of S cycling involving microbial SO{sub 4} reduction, abiotic oxidation of H{sub 2}S to S{sup 0} by Mn(IV), followed by microbial disproportionation of S{sup 0} to H{sub 2}S and SO{sub 4}. The high pH, Ca depletion, MnCO{sub 3} saturation, and presence of S{sup 0} in Lahontan Valley groundwater may be consequences of the anaerobic S cycling. Consistent with data from naturally-enriched wells in Florida, {sup 210}Po activities begin to decrease when aqueous sulfide species begin to accumulate. This may be due to formation and precipitation of PoS, however, Eh-pH diagrams suggest PoS would not be stable in study-area groundwater. An alternative explanation for the study area

  17. Controlled synthesis and photocatalytic properties of rhombic dodecahedral Ag3PO4 with high surface energy

    Science.gov (United States)

    Xie, Yao; Huang, Zhaohui; Zhang, Zhijie; Zhang, Xiaoguang; Wen, Ruilong; Liu, Yangai; Fang, Minghao; Wu, Xiaowen

    2016-12-01

    In this study, a series of Ag3PO4 photocatalysts with different contents of rhombic dodecahedral particles were prepared in one pot by a facile, novel hydrothermal method using ethylene glycol (EG), which served as both a morphology modifier and reducing agent. The effects of EG content on the morphologies of Ag3PO4 photocatalysts were discussed. The photocatalytic activity of the Ag3PO4 photocatalysts was evaluated by the degradation of methylene blue trihydrate under visible-light irradiation. With the use of 0.8% EG in the reaction solvent, the sample exhibited excellent photocatalytic activity, attributed to the high amount of rhombic dodecahedral Ag3PO4 particles with a high exposure of the {110} facets and high surface energy. The surface energy of the {110} facets was 1.31 J/m2, greater than that of the {100} facet (1.12 J/m2). However, with 1% EG in the reaction solvent, although the Ag3PO4 photocatalysts were composed of a majority of rhombic dodecahedral Ag3PO4 particles, tiny Ag particles formed from Ag+ under the action of EG attached on the surface of the sample decreased the absorption of visible light, resulting in low photocatalytic activity.

  18. Trois poètes corses

    Directory of Open Access Journals (Sweden)

    2012-06-01

    Full Text Available On doit les traductions de ces poèmes (y compris des siens au poète Francescu-Micheli Durazzo qui œuvre avec obstination pour la poésie corse (A filetta, onze poètes corses contemporains, aux éditions Phi ; et le numéro spécial « Poètes corses » de la revue basque Zurgai, Bilbao, avec une très éclairante préface du même. Je me suis permis une ou deux très minimes interventions dues à ma sensibilité personnelle ; elles traduisent, sous une forme moins parfaite que la sienne, mon souci de col...

  19. Redetermination of AgPO(3).

    Science.gov (United States)

    Terebilenko, Katherina V; Zatovsky, Igor V; Ogorodnyk, Ivan V; Baumer, Vyacheslav N; Slobodyanik, Nikolay S

    2011-02-09

    Single crystals of silver(I) polyphosphate(V), AgPO(3), were prepared via a phospho-ric acid melt method using a solution of Ag(3)PO(4) in H(3)PO(4). In comparison with the previous study based on single-crystal Weissenberg photographs [Jost (1961 ▶). Acta Cryst. 14, 779-784], the results were mainly confirmed, but with much higher precision and with all displacement parameters refined anisotropically. The structure is built up from two types of distorted edge- and corner-sharing [AgO(5)] polyhedra, giving rise to multidirectional ribbons, and from two types of PO(4) tetra-hedra linked into meandering chains (PO(3))(n) spreading parallel to the b axis with a repeat unit of four tetra-hedra. The calculated bond-valence sum value of one of the two Ag(I) ions indicates a significant strain of the structure.

  20. Redetermination of AgPO3

    Science.gov (United States)

    Terebilenko, Katherina V.; Zatovsky, Igor V.; Ogorodnyk, Ivan V.; Baumer, Vyacheslav N.; Slobodyanik, Nikolay S.

    2011-01-01

    Single crystals of silver(I) polyphosphate(V), AgPO3, were prepared via a phospho­ric acid melt method using a solution of Ag3PO4 in H3PO4. In comparison with the previous study based on single-crystal Weissenberg photographs [Jost (1961 ▶). Acta Cryst. 14, 779–784], the results were mainly confirmed, but with much higher precision and with all displacement parameters refined anisotropically. The structure is built up from two types of distorted edge- and corner-sharing [AgO5] polyhedra, giving rise to multidirectional ribbons, and from two types of PO4 tetra­hedra linked into meandering chains (PO3)n spreading parallel to the b axis with a repeat unit of four tetra­hedra. The calculated bond-valence sum value of one of the two AgI ions indicates a significant strain of the structure. PMID:21522230

  1. Leatherback Isotopes

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — SWFSC is currently working on a project identifying global marine isotopes using leatherback turtles (Dermochelys coriacea) as the indicator species. We currently...

  2. Isotopic chirality

    Energy Technology Data Exchange (ETDEWEB)

    Floss, H.G. [Univ. of Washington, Seattle, WA (United States)

    1994-12-01

    This paper deals with compounds that are chiral-at least in part, due to isotope substitution-and their use in tracing the steric course of enzyme reaction in vitro and in vivo. There are other applications of isotopically chiral compounds (for example, in analyzing the steric course of nonenzymatic reactions and in probing the conformation of biomolecules) that are important but they will not be discussed in this context.

  3. Isotopic Paleoclimatology

    Science.gov (United States)

    Bowen, R.

    Paleotemperature scales were calculated by H. C. Urey and others in the 1950s to assess past temperatures, and later work using the stable isotopes of oxygen, hydrogen, and carbon employed standards such as Peedee belemnite (PDB) and Standard Mean Ocean Water (SMOW). Subsequently, subjects as diverse as ice volume and paleotemperatures, oceanic ice and sediment cores, Pleistocene/Holocene climatic changes, and isotope chronostratigraphy extending back to the Precambrian were investigated.

  4. Behavior of 210Po and 210Pb in Shallow Water Region of Mersing Estuary, Johor, Malaysia

    Directory of Open Access Journals (Sweden)

    Noor Affizah Bujang Saili

    2014-06-01

    Full Text Available 210Po and 210Pb activities were determined in dissolved and particulate phases in order to understand the behavior of both natural radionuclides in shallow water regions such as Mersing Estuary. Strong statistical correlations between the distribution coefficient values of polonium and lead in dissolved phases with SPM proved that the natural nuclides of polonium and lead have a high affinity to suspended particle materials in the water column, where the SPM acts as a carrier to transport and remove natural isotopes of polonium and lead from their geochemical behavior. However a low statistical correlation (r=0.414 found between chlorophyll-a with an activity ratio of 210Po/210Pb and SPM implies that the enrichment of 210Po was not associated with the abundance of chlorophyll-a. But a strong correlation between soluble reactive phosphorus (SRP and 210Po in the dissolved phase proved that the contribution of phosphate element as catalysis increasing the activity levels of 210Po at coastal waters.

  5. Ultraviolet luminescence of ScPO4, AlPO4 and GaPO4 crystals.

    Science.gov (United States)

    Trukhin, Anatoly N; Shmits, Krishjanis; Jansons, Janis L; Boatner, Lynn A

    2013-09-25

    The luminescence of self-trapped excitons (STEs) was previously observed and described for the case of tetragonal-symmetry ScPO4 single crystals. The subject band in this material is situated in the UV spectral range of ∼210 nm or ∼5.8 eV. In the present work, we are both expanding this earlier luminescence study and seeking to identify similar luminescence phenomena in other orthophosphate crystals, i.e., AlPO4 and GaPO4. These efforts have proven to be successful--in spite of the structural differences between these materials and ScPO4. Specifically we have found that for AlPO4 and GaPO4, in addition to an α-quartz-like STE, there is a UV luminescence band that is similar in position and decay properties to that of ScPO4 crystals. Potentially this represents an STE in AlPO4 and GaPO4 crystals that is analogous to the STE of ScPO4 and other orthophosphates. The decay kinetics of the UV luminescence of ScPO4 was studied over a wide temperature range from 8 to 300 K, and they exhibited some unusual decay characteristics when subjected to pulses from an F2 excimer laser (157 nm). These features could be ascribed to a triplet state of the STE that is split in a zero magnetic field. A fast decay of the STE was detected as well, and therefore, we conclude that, in addition to the slow luminescence corresponding to a transition from the triplet state, there are singlet-singlet transitions of the STE. Time-resolved spectra of the slow and fast decay exhibit a small shift (∼0.15 eV) indicating that the singlet-triplet splitting is small and the corresponding wavefunction of the STE is widely distributed over the atoms of the ScPO4 crystal where the STE is created.

  6. Stages of weathering mantle formation from carbonate rocks in the light of rare earth elements (REE) and Sr-Nd-Pb isotopes

    Science.gov (United States)

    Hissler, Christophe; Stille, Peter

    2015-04-01

    Weathering mantles are widespread and include lateritic, sandy and kaolinite-rich saprolites and residuals of partially dissolved rocks. These old regolith systems have a complex history of formation and may present a polycyclic evolution due to successive geological and pedogenetic processes that affected the profile. Until now, only few studies highlighted the unusual high content of associated trace elements in weathering mantles originating from carbonate rocks, which have been poorly studied, compared to those developing on magmatic bedrocks. For instance, these enrichments can be up to five times the content of the underlying carbonate rocks. However, these studies also showed that the carbonate bedrock content only partially explains the soil enrichment for all the considered major and trace elements. Up to now, neither soil, nor saprolite formation has to our knowledge been geochemically elucidated. Therefore, the aim of this study was to examine more closely the soil forming dynamics and the relationship of the chemical soil composition to potential sources. REE distribution patterns and Sr-Nd-Pb isotope ratios have been used because they are particularly well suited to identify trace element migration, to recognize origin and mixing processes and, in addition, to decipher possible anthropogenic and/or "natural" atmosphere-derived contributions to the soil. Moreover, leaching experiments have been applied to identify mobile phases in the soil system and to yield information on the stability of trace elements and especially on their behaviour in these Fe-enriched carbonate systems. All these geochemical informations indicate that the cambisol developing on such a typical weathering mantle ("terra fusca") has been formed through weathering of a condensed Bajocian limestone-marl facies. This facies shows compared to average world carbonates important trace element enrichments. Their trace element distribution patterns are similar to those of the soil

  7. Zinc isotopic compositions of breast cancer tissue.

    Science.gov (United States)

    Larner, Fiona; Woodley, Laura N; Shousha, Sami; Moyes, Ashley; Humphreys-Williams, Emma; Strekopytov, Stanislav; Halliday, Alex N; Rehkämper, Mark; Coombes, R Charles

    2015-01-01

    An early diagnostic biomarker for breast cancer is essential to improve outcome. High precision isotopic analysis, originating in Earth sciences, can detect very small shifts in metal pathways. For the first time, the natural intrinsic Zn isotopic compositions of various tissues in breast cancer patients and controls were determined. Breast cancer tumours were found to have a significantly lighter Zn isotopic composition than the blood, serum and healthy breast tissue in both groups. The Zn isotopic lightness in tumours suggests that sulphur rich metallothionein dominates the isotopic selectivity of a breast tissue cell, rather than Zn-specific proteins. This reveals a possible mechanism of Zn delivery to Zn-sequestering vesicles by metallothionein, and is supported by a similar signature observed in the copper isotopic compositions of one breast cancer patient. This change in intrinsic isotopic compositions due to cancer has the potential to provide a novel early biomarker for breast cancer.

  8. Superconducting Coil of Po Dipole

    CERN Multimedia

    1983-01-01

    The Po superconducting dipole was built as a prototype beam transport magnet for the SPS extracted proton beam P0. Its main features were: coil aperture 72 mm, length 5 m, room-temperature yoke, NbTi cable conductor impregnated with solder, nominal field 4.2 T at 4.7 K (87% of critical field). It reached its nominal field without any quench.After this successful test up to its nominal field of 4.2 T, the power was not raised to reach a quench. The magnet was not installed in a beam and had no other further use. Nevertheless its construction provided knowledges and experience which became useful in the design and construction of the LHC magnets. The photo shows a detail of the inner layer winding before superposing the outer layer to form the complete coil of a pole. Worth noticing is the interleaved glass-epoxy sheet (white) with grooved channels for the flow of cooling helium. See also 8211532X.

  9. Deuterium isotope effects on acid ionization and transition metal hydrolysis at reactor conditions by Raman spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Yacyshyn, M.; Madekufamba, M.; Tremaine, P. [Univ. of Guelph, Dept. of Chemistry, Guelph, Ontario (Canada)

    2011-07-01

    This paper reports the preliminary measurements from an experimental study to measure the small differences between light (H{sub 2}O) and heavy (D{sub 2}O) water under reactor operating conditions (250-300 {sup o}C, 10 MPa), using Raman spectroscopy. The deuterium isotope effect δpK = pK{sub D2O} - pK{sub H2O}, for sodium bisulphate NaDSO{sub 4} and phosphoric acid D{sub 3}PO{sub 4}, has now been determined at temperatures of 25 {sup o}C and 80 {sup o}C by measuring the isotropic Raman spectra at different concentrations. The results for the pK and ΔpK at 25 {sup o}C agree with the literature, confirming the reliability of the method. High temperature cells have been constructed. (author)

  10. Isotopic variants of light and heavy L-pyroglutamic acid succinimidyl esters as the derivatization reagents for DL-amino acid chiral metabolomics identification by liquid chromatography and electrospray ionization mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Mochizuki, Toshiki; Todoroki, Kenichiro; Inoue, Koichi; Min, Jun Zhe; Toyo’oka, Toshimasa, E-mail: toyooka@u-shizuoka-ken.ac.jp

    2014-02-06

    Graphical abstract: -- Highlights: •Isotopic variants of chiral labeling reagents were newly synthesized. •Analysis of DL-amino acids was performed by UPLC–ESI–MS/MS. •Highly efficient enantioseparation and detection of DL-amino acids were performed. •Differential analysis of DL-amino acid was successfully performed in real samples. -- Abstract: L-Pyroglutamic acid succinimidyl ester (L-PGA-OSu) and its isotopic variant (L-PGA[d{sub 5}]-OSu) were newly synthesized and evaluated as the chiral labeling reagents for the enantioseparation of amino acids, in terms of separation efficiency by reversed-phase chromatography and detection sensitivity by ESI-MS/MS. The enantiomers of amino acids were easily labeled with the reagents at 60 °C within 10 min in an alkaline medium containing triethylamine. Although all the diastereomers derived from 18 proteolytic amino acids could not be satisfactorily separated, the pairs of 9 amino acids were completely separated by reversed-phase chromatography using the small particle (1.7 μm) ODS column (Rs = 1.95–8.05). The characteristic daughter ions, i.e., m/z 84.04 and m/z 89.04, were detected from all the derivatives by the collision induced dissociation of the protonated molecular ions. A highly sensitive detection at a low-fmol level (0.5–3.2 fmol) was also obtained from the selected reaction monitoring (SRM) chromatograms. An isotope labeling strategy using light and heavy L-PGA-OSu for the differential analysis of the DL-amino acids in different sample groups is also presented in this paper. The differential analysis of biological sample (i.e., human serum) and food product (i.e., yogurt) were tried to demonstrate the efficiency of the proposed method. The ratios of the DL-amino acids in human serum samples, spiked with the different concentrations of D-amino acids, were determined by the procedures using L-PGA-OSu and L-PGA[d{sub 5}]-OSu. The D/L ratios in the two sample groups at different concentrations of

  11. Production of very neutron-deficient isotopes near sup 1 sup 0 sup 0 Sn via reactions involving light-particle and cluster emission

    CERN Document Server

    La Commara, M; D'Onofrio, A; Gadea, A; Glogowski, M; Jarillo-Herrero, P; Belcari, N; Borcea, R; De Angelis, G; Fahlander, C; aGórska, M; Grawe, H; Hellström, M; Kirchner, R; Rejmund, M; Roca, V; Roeckl, E; Romano, M; Rykaczewski, K; Schmidt, K; Terrasi, F

    2000-01-01

    The production of very neutron-deficient isotopes near sup 1 sup 0 sup 0 Sn has been investigated by using on-line mass separation of evaporation residues produced by heavy-ion induced complete-fusion reactions. We measured the cross sections for sup 9 sup 9 Cd, sup 1 sup 0 sup 0 In, sup 1 sup 0 sup 1 Sn and sup 1 sup 0 sup 2 In via sup 5 sup 8 Ni+ sup 5 sup 8 Ni fusion reactions followed by cluster emission, and via sup 5 sup 8 Ni+ sup 5 sup 0 Cr fusion reactions accompanied by evaporation of protons, neutrons or alpha particles. Both types of reactions yield similar cross sections for the production of exotic nuclei near sup 1 sup 0 sup 0 Sn. The data are discussed in comparison with results obtained from statistical-model calculations.

  12. Perfect softening of the ferroelectric mode in the isotope-exchanged strontium titanate of SrTi18O3 studied by light scattering.

    Science.gov (United States)

    Takesada, M; Itoh, M; Yagi, T

    2006-06-09

    The mode of the isotope-induced ferroelectric strontium titanate shows a perfect softening at the ferroelectric phase transition temperature , where the frequency of the underdamped mode approaches completely to zero within the instrumental resolution. The spectra of the Raman inactive soft mode have been successfully observed owing to local symmetry breaking and by long-term accumulation of the spectral intensity with a high resolution technique. The mechanism of the phase transition is concluded to be an ideal displacive-type accompanied with perfect softening of the Slater-type polar mode. The difference between the soft mode behavior of and indicates that the origin of the quantum paraelectric state of lies in the quantum fluctuation of the oxide octahedron in the perovskite structure.

  13. El lenguaje poético

    Directory of Open Access Journals (Sweden)

    Alfonso Hanssen

    1966-03-01

    Full Text Available Me parece absurdo pretender hallar la intención poética en cualesquiera rastros de la historia, por el solo hecho de que en ellos se afirma cierta reconditez que los hace misteriosos.

  14. Lifetime measurement in {sup 195}Po

    Energy Technology Data Exchange (ETDEWEB)

    Grahn, T.; Page, R.D. [University of Liverpool, Department of Physics, Oliver Lodge Laboratory, Liverpool (United Kingdom); Dewald, A.; Jolie, J.; Melon, B.; Pissulla, T. [Universitaet zu Koeln, Institut fuer Kernphysik, Koeln (Germany); Greenlees, P.T.; Jakobsson, U.; Jones, P.; Julin, R.; Juutinen, S.; Ketelhut, S.; Leino, M.; Nyman, M.; Peura, P.; Rahkila, P.; Saren, J.; Scholey, C.; Sorri, J.; Uusitalo, J. [University of Jyvaeskylae, Department of Physics, P.O. Box 35, Jyvaeskylae (Finland); Kroell, T.; Kruecken, R.; Maierbeck, P. [TU Muenchen, Physik-Department E12, Garching (Germany)

    2009-03-15

    The lifetime of the 17/2{sup +} yrast state in {sup 195}Po has been measured using the recoil distance Doppler-shift technique to be {tau}=43(11) ps. The lifetime was extracted from the singles {gamma}-ray spectra obtained by using the recoil-decay tagging method. The present work provides more information of the coupling schemes, shapes and configuration mixing in neutron-deficient odd-mass Po nuclei. (orig.)

  15. A cell wall-bound anionic peroxidase, PtrPO21, is involved in lignin polymerization in Populus trichocarpa

    Energy Technology Data Exchange (ETDEWEB)

    Lin, Chien-Yuan; Li, Quanzi; Tunlaya-Anukit, Sermsawat; Shi, Rui; Sun, Ying-Hsuan; Wang, Jack P.; Liu, Jie; Loziuk, Philip; Edmunds, Charles W.; Miller, Zachary D.; Peszlen, Ilona; Muddiman, David C.; Sederoff, Ronald R.; Chiang, Vincent L.

    2016-03-11

    Class III peroxidases are members of a large plant-specific sequence-heterogeneous protein family. Several sequence-conserved homologs have been associated with lignin polymerization in Arabidopsis thaliana, Oryza sativa, Nicotiana tabacum, Zinnia elegans, Picea abies, and Pinus sylvestris. In Populus trichocarpa, a model species for studies of wood formation, the peroxidases involved in lignin biosynthesis have not yet been identified. To do this, we retrieved sequences of all PtrPOs from Peroxibase and conducted RNA-seq to identify candidates. Transcripts from 42 PtrPOs were detected in stem differentiating xylem (SDX) and four of them are the most xylem-abundant (PtrPO12, PtrPO21, PtrPO42, and PtrPO64). PtrPO21 shows xylem-specific expression similar to that of genes encoding the monolignol biosynthetic enzymes. Using protein cleavage-isotope dilution mass spectrometry, PtrPO21 is detected only in the cell wall fraction and not in the soluble fraction. Downregulated transgenics of PtrPO21 have a lignin reduction of ~20% with subunit composition (S/G ratio) similar to wild type. The transgenics show a growth reduction and reddish color of stem wood. The modulus of elasticity (MOE) of the stems of the downregulated PtrPO21-line 8 can be reduced to ~60% of wild type. Differentially expressed gene (DEG) analysis of PtrPO21 downregulated transgenics identified a significant overexpression of PtPrx35, suggesting a compensatory effect within the peroxidase family. No significant changes in the expression of the 49 P. trichocarpa laccases (PtrLACs) were observed.

  16. A novel molecular sieve supporting material for enhancing activity and stability of Ag3PO4 photocatalyst

    Science.gov (United States)

    Wu, Qiang; Wang, Peifu; Niu, Futao; Huang, Cunping; Li, Yang; Yao, Weifeng

    2016-08-01

    A small-pore silicon-substituted silicon aluminum phosphate (SAPO-34) molecular sieve, for the first time, is reported to significantly increase both the activity and life span of Ag3PO4 photocatalyst for visible-light degradation of methylene blue (MB) and rhodamine B (RhB). Results show that 60 wt.% Ag3PO4/SAPO-34 exhibits the highest photocatalytic degradation efficiencies for both MB (91.0% degradation within 2.0 min) and RhB (91.0% degradation within 7.0 min). In comparison, pure Ag3PO4 powder photocatalyst requires 8.0 min and 12.0 min for decomposing 91.0% of MB and RhB, respectively. During MB degradation the rate constant for 60 wt.% Ag3PO4/SAPO-34 increases 317.2% in comparison with the rate constant of pure Ag3PO4. This activity is also much higher than literature reported composite or supported Ag3PO4 photocatalysts. In three photocatalytic runs for the degradation of RhB, the rate constant for 60 wt.% Ag3PO4/SAPO-34 reduces from 0.33 to 0.18 min-1 (45.5% efficiency loss). In contrast, the rate constant of pure Ag3PO4 catalyst decreases from 0.2 to 0.07 min-1 (80.0% efficiency loss). All experimental results have shown that small pores and zero light absorption loss of SAPO-34 molecular sieves minimize Ag3PO4 loading, enhance photocatalytic activity and prolong the lifespan of Ag3PO4 photocatalyst.

  17. Hydrothermal synthesis and luminescence properties of Eu3+and Sm3+codoped BiPO4

    Institute of Scientific and Technical Information of China (English)

    钟剑明; 赵韦人; 蓝立财; 王建青

    2014-01-01

    Eu3+/Sm3+codoped BiPO4 phosphors were synthesized via a facile hydrothermal method with surfactant-free environment. The X-ray diffraction analysis demonstrated that the samples possessed the standard BiPO4 monoclinic structure. Scanning electron microscopy images showed that all samples composed of well-dispersed, micrometer-sized crystals with shuttle-like shape. Energy transfer from Sm3+to Eu3+was confirmed by the luminescence spectra and the decay processes of Sm3+ 4G5/2→6H5/2 emission. Or-ange-red luminescence could be obtained in Eu3+/Sm3+codoped BiPO4 phosphors. The average lifetime of Sm3+ 4G5/2→6H5/2 emis-sion decreased from 2.70 ms in BiPO4:0.03Sm3+ to 2.37 ms in BiPO4:0.03Sm3+,0.05Eu3+. The strong and wide absorption band around 395 nm, originating from both 7F0→5L6 transition of Eu3+and 6H5/2→4K11/2 transition of Sm3+, endowed BiPO4:Eu3+,Sm3+phosphors with the potential application in the fields of near UV-excited white-light-emitting diodes.

  18. Angular Accelerating White Light

    CSIR Research Space (South Africa)

    Dudley, Angela L

    2015-08-01

    Full Text Available Shaping XVI, 958104, San Diego, California, United States, 09 August 2015 Angular Accelerating White Light Angela Dudley*a,b, Christian Vetterc , Alexander Szameitc , and Andrew Forbesa,b a CSIR National Laser Centre, PO Box 395, Pretoria 0001...

  19. Investigation Of Water Assisted Phase Transformation Process From AlPO4-5 to AlPO4-tridymite

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Suochang; Zhao, Zhenchao; Hu, Mary Y.; Han, Xiuwen; Hu, Jian Z.; Bao, Xinhe

    2016-03-15

    Water assisted phase transformation process from crystalized AlPO4-5 to AlPO4-tridymite was studied by the combination of X-ray diffraction (XRD), Scanning Electron Microscopy (SEM) and in situ multinuclear MAS NMR. It is found that water first activates the residue amorphous aluminophosphate in crystalized AlPO4-5 sample through hydrolysis and condensation reactions. Then the activated aluminophosphate species reassemble into AlPO4-tridymite crystalline. Meanwhile, AlPO4-5 transforms into orthorhombic phase during heating process. With further crystallization of AlPO4-tridymite, the amorphous phase is gradually consumed, and mass transportation between AlPO4-5 and AlPO4-tridymite is established through gradually amorphization of AlPO4-5. Finally, most of the AlPO4-5 transforms into the thermodynamically stable dense phase AlPO4-tridymite.

  20. The Twinflower (Linnaea borealis L. in the northern part of the Południowopodlaska Lowland

    Directory of Open Access Journals (Sweden)

    Ciosek Marek Tadeusz

    2015-06-01

    Full Text Available Linnaea borealis, the twinflower, is considered a critically endangered species in the Południowopodlaska Lowland. The disappearance of the twinflower is mainly caused by habitat changes resulting from forest management, but also light deficiency due to the increase in canopy cover and growth of the shrub layer (processes of succession.

  1. Linking the Fe-, Mo-, and Cr isotope records with the multiple S isotope record of Archean sedimentary rocks

    Science.gov (United States)

    Ohmoto, H.; Watanabe, Y.

    2011-12-01

    Researchers have interpreted the isotopic data of redox sensitive elements (e.g., Fe, Mo and Cr) in Archean- and Proterozoic-aged sedimentary rocks within a framework of an atmospheric O2 evolution model that relied on an interpretation of the multiple sulfur isotopic record of sedimentary rocks. The current paradigm is that the anomalous isotopic fractionations of sulfur (AIF-S, or MIF-S) in sedimentary rocks were created by the UV photolysis of volcanic SO2 in an O2-poor (i.e., pO2 atmosphere, and that the rise of atmospheric pO2 to > 1 ppm occurred at ~2.45 Ga. However, this paradigm has recently encountered the following serious problems: (1) UV photolysis of SO2 by a broad-band UV lamp, which simulates the UV spectra of the sun light, produced the δ34S-Δ33S values for the S0 and SO4 that are significantly different from >90% of data on natural samples. (2) Many Archean-age sedimentary rocks do not exhibit AIF-S signatures. (3) Strong AIF-S signatures are typically found in organic C- and pyrite rich Archean-age black shales that were altered by submarine hydrothermal fluids during the early diagenetic stage of the rocks. (4) H2S, rather than SO2, was probably the dominant S-bearing volcanic gas on an anoxic Earth. Yet, UV photolysis of H2S does not generate AIF-S. (5) Some post-2.0 Ga natural samples were found to possess strong AIF-S signatures, such as sulfates in air pollutants that were produced by coal burning in an oxygen-rich atmosphere. Lasaga et al. (2008) demonstrated theoretically that chemisorption reactions between some solid surfaces and S-bearing aqueous (or gaseous) species, such as between organic matter and aqueous sulfate, may generate AIF-S. Watanabe et al. (2009; in prep.) demonstrated experimentally that reactions between simple amino acid crystals and sulfate under hydrothermal conditions produced AIF-S signatures that matched with more than 90% of data on natural samples. These studies, as well as the observed correlations between the

  2. Synthesis of few-layer MoS2 nanosheet-loaded Ag3PO4 for enhanced photocatalytic activity.

    Science.gov (United States)

    Song, Yanhua; Lei, Yucheng; Xu, Hui; Wang, Cheng; Yan, Jia; Zhao, Haozhu; Xu, Yuanguo; Xia, Jiexiang; Yin, Sheng; Li, Huaming

    2015-02-21

    Novel few-layer MoS2/Ag3PO4 composites were fabricated. The results indicated that Ag3PO4 nanoparticles were directly formed on the surface of few-layer MoS2. The physical and chemical properties of the few-layer MoS2/Ag3PO4 composite photocatalysts were tested in order to investigate the effects of few-layer MoS2 on the photocatalytic activity of Ag3PO4. The photocatalytic activity of the few-layer MoS2/Ag3PO4 composites was evaluated by the photocatalytic degradation of Rhodamine B (RhB) and bisphenol A (BPA) under visible light irradiation. The photocatalytic activity of the few-layer MoS2/Ag3PO4 composites was higher than that of pure Ag3PO4. The optimal few-layer MoS2 content for the organic pollutant degradation of the heterojunction structures was determined. The synergic effect between few-layer MoS2 and Ag3PO4 was found to lead to an improved photogenerated carrier separation. The stability and the possible photocatalytic mechanism of the composites were also discussed.

  3. De-excitation of the strongly coupled band in 177Au and implications for core intruder configurations in the light Hg isotopes

    Science.gov (United States)

    Venhart, M.; Ali, F. A.; Ryssens, W.; Wood, J. L.; Joss, D. T.; Andreyev, A. N.; Auranen, K.; Bally, B.; Balogh, M.; Bender, M.; Carroll, R. J.; Easton, J. L.; Greenlees, P. T.; Grahn, T.; Heenen, P.-H.; HerzáÅ, A.; Jakobsson, U.; Julin, R.; Juutinen, S.; Kĺč, D.; Konki, J.; Lawrie, E.; Leino, M.; Matoušek, V.; McPeake, C. G.; O'Donnell, D.; Page, R. D.; Pakarinen, J.; Partanen, J.; Peura, P.; Rahkila, P.; Ruotsalainen, P.; Sandzelius, M.; Sarén, J.; Sayǧi, B.; Sedlák, M.; Scholey, C.; Sorri, J.; Stolze, S.; Thornthwaite, A.; Uusitalo, J.; Veselský, M.

    2017-06-01

    Excited states in the proton-unbound nuclide 177Au were populated in the 92Mo(88Sr, p 2 n ) reaction and identified using the Jurogam-II and GREAT spectrometers in conjunction with the RITU gas-filled separator at the University of Jyväskylä Accelerator Laboratory. A strongly coupled band and its decay path to the 11 /2-α -decaying isomer have been identified using recoil-decay tagging. Comparisons with cranked Hartree-Fock-Bogoliubov (HFB) calculations based on Skyrme energy functionals suggest that the band has a prolate deformation and is based upon coupling the odd 1 h11 /2 proton hole to the excited 02+ configuration in the 178Hg core. Although these configurations might be expected to follow the parabolic trend of core Hg(02+) states as a function of neutron number, the electromagnetic decay paths from the strongly coupled band in 177Au are markedly different from those observed in the heavier isotopes above the midshell. This indicates that a significant change in the structure of the underlying A +1Hg core occurs below the neutron midshell.

  4. Measurement of the He 1s2s (1)S(0) isotopic shift using a tunable VUV anti-Stokes light source.

    Science.gov (United States)

    Falcone, R W; Willison, J R; Young, J F; Harris, S E

    1978-11-01

    We describe a high-resolution, vacuum-ultraviolet spectroscopic technique based on a tunable, narrow-band, VUV, spontaneous anti-Stokes light source. The technique was used to measure the absolute energies of the 1s2s (1)S(0) states of (3)He and (4)He; the 1s2s (1)S(0) level of (3)He is 7.8 +/- 0.5 cm(-1) below that of (4)He.

  5. Radioactive {sup 210}Po in magnesium supplements

    Energy Technology Data Exchange (ETDEWEB)

    Struminska-Parulska, Dagmara Ida [Gdansk Univ. (Poland). Environmental Chemistry and Radiochemistry Chair

    2016-08-01

    The aim of this pioneer study was to determine polonium {sup 210}Po in the most popular magnesium supplements in Poland and estimate the possible related dose assessment to the consumers. The analyzed magnesium pharmaceutics contained organic or inorganic magnesium compounds; some from natural sources. The objectives of this research were to investigate the naturally occurring {sup 210}Po activity concentrations in magnesium supplements, find the correlations between {sup 210}Po concentration in medicament and magnesium chemical form, and calculate the effective radiation dose connected to analyzed magnesium supplement consumption. The highest {sup 210}Po activity concentrations were determined in mineral tablets made from sedimentary rocks, namely dolomite - 3.84 ± 0.15 mBq g{sup -1} (sample Mg17). The highest annual radiation dose from {sup 210}Po taken with 1 tablet of magnesium supplement per day or with 400 mg of pure Mg daily would come from sample Mg17 (dolomite) - 1.35 ± 0.5 and 8.44 ± 0.33 μSv year{sup -1} respectively.

  6. Una poética del pliegue

    Directory of Open Access Journals (Sweden)

    Ana Porrúa

    2000-11-01

    Full Text Available La producción de Juan Gelman-de Violín y otras cuestiones a Relaciones- puede inscribirse dentro de la poética sesentista caracterizada por la hegemonía de la narración y la apertura del discurso poético al resto de los discursos sociales, pero también establece una compleja relación con las vanguardias históricas. La noción de pliegue permite revisar las articulaciones de este conflicto; como espacio el pliegue separa ambas poéticas, la "coloquialista" y vanguardista, que pueden leerse en el interior del corpus propuesto en estado puro, yuxtapuestas, o bajo la forma del cruce que instala la polémica entre libros o textos de un mismo libro. La idea depliegue como rasgo operatorio permite, por su parte, revisar la relación entre ambas poéticas en el interior de un poema, focalizando la materia, el lenguaje. En este caso la poética vanguardista funciona como cuestionamiento de la linealidad del texto sesentista.

  7. Una poética del pliegue

    Directory of Open Access Journals (Sweden)

    Ana Porrúa

    2001-11-01

    Full Text Available La producción de Juan Gelman-de Violín y otras cuestiones a Relaciones- puede inscribirse dentro de la poética sesentista caracterizada por la hegemonía de la narración y la apertura del discurso poético al resto de los discursos sociales, pero también establece una compleja relación con las vanguardias históricas. La noción de pliegue permite revisar las articulaciones de este conflicto; como espacio el pliegue separa ambas poéticas, la "coloquialista" y vanguardista, que pueden leerse en el interior del corpus propuesto en estado puro, yuxtapuestas, o bajo la forma del cruce que instala la polémica entre libros o textos de un mismo libro. La idea depliegue como rasgo operatorio permite, por su parte, revisar la relación entre ambas poéticas en el interior de un poema, focalizando la materia, el lenguaje. En este caso la poética vanguardista funciona como cuestionamiento de la linealidad del texto sesentista.

  8. Fabrication and Photocatalytic Activity of Ag3PO4-TiO2 Heterostructural Nanotube Arrays

    Institute of Scientific and Technical Information of China (English)

    MO Yanping; CHEN Feng; YANG Yunyun; SONG Jia; XU Qiong; XU Ying

    2016-01-01

    To extend the absorption capability of TiO2 into visible light region and inhibit the recombination of photogenerated electrons and holes, we put forward an effective strategy of the coupling of TiO2 with a suitable semiconductor that possesses a narrow band gap. Meanwhile, Ag3PO4-TiO2 heterostructural nanotube arrays were prepared by the two-step anodic oxidation to obtain the TiO2 nanotube arrays and then by a deposition-precipitation method to load Ag3PO4. The samples were characterized by ifeld emission scanning electron microscopy (FESEM), energy dispersive spectrometry (EDS), X-ray diffraction (XRD), and UV-vis diffuse relfectance spectroscopy (UV-vis DRS). The experimental results showed that Ag3PO4nanoparticles were uniformly dispersed on the highly ordered TiO2 nanotube arrays, which increased the visible-light absorption of TiO2 photocatalyst. The photocurrent density and photocatalytic degradation of methyl orange indicated that the performance of Ag3PO4-TiO2 heterostructural nanotube arrays was better than that of the TiO2 nanotube arrays, which could be attributed to the effective electron-hole separation and the improved utilization of visible light.

  9. (Gd,Yb,Tb)PO4 up-conversion nanocrystals for bimodal luminescence-MR imaging

    Science.gov (United States)

    Debasu, Mengistie L.; Ananias, Duarte; Pinho, Sonia L. C.; Geraldes, Carlos F. G. C.; Carlos, Luís D.; Rocha, João

    2012-07-01

    Up-conversion (Gd,Yb,Tb)PO4 materials and their potential for bimodal imaging have received little attention in the literature. Herein, we report the first study on the up-conversion emission of (Gd,Yb,Tb)PO4 nanocrystals synthesized via a hydrothermal method at 150 °C. These materials exhibit ultraviolet, blue and green up-conversion emissions upon excitation with a 980 nm continuous wave laser diode. The intensity of the blue-emission band at 479 nm, ascribed to the cooperative up-conversion emission of a pair of excited Yb3+ ions, depends on the Yb3+/Tb3+ concentration ratio, calcination temperature and particle size. Strong green up-conversion emission of Tb3+ is observed at 543 nm for the 5D4 --> 7F5 transition. Relaxometry measurements reveal that the nanocrystals are efficient T2-weighted (negative) contrast agents which, combined with visible-light emission generated by infrared excitation, affords them considerable potential for being used in bimodal, photoluminescence-magnetic resonance, imaging.Up-conversion (Gd,Yb,Tb)PO4 materials and their potential for bimodal imaging have received little attention in the literature. Herein, we report the first study on the up-conversion emission of (Gd,Yb,Tb)PO4 nanocrystals synthesized via a hydrothermal method at 150 °C. These materials exhibit ultraviolet, blue and green up-conversion emissions upon excitation with a 980 nm continuous wave laser diode. The intensity of the blue-emission band at 479 nm, ascribed to the cooperative up-conversion emission of a pair of excited Yb3+ ions, depends on the Yb3+/Tb3+ concentration ratio, calcination temperature and particle size. Strong green up-conversion emission of Tb3+ is observed at 543 nm for the 5D4 --> 7F5 transition. Relaxometry measurements reveal that the nanocrystals are efficient T2-weighted (negative) contrast agents which, combined with visible-light emission generated by infrared excitation, affords them considerable potential for being used in bimodal

  10. Forenzika elektronske pošte

    OpenAIRE

    Milorad S. Markagić

    2013-01-01

    U najopštijem smislu digitalna forenzika može se definisati kao skup metoda za prikupljanje, analizu i prezentaciju digitalnih dokaza koji se mogu pronaći na računarima, serverima, u računarskim mrežama, bazama podataka, mobilnim uređajima i svim drugim elektronskim uređajima na kojima se čuvaju podaci. U ovom radu su opisane metode prikupljanja digitalnih dokaza u elektronskoj pošti i njihova analiza. Uvod Elektronska pošta se kao dokazni materijal pojavljuje u velikom broju kako građanskih ...

  11. PoPSat: The Polar Precipitation Satellite Mission

    Science.gov (United States)

    Binder, Matthias J.; Agten, Dries; Arago-Higueras, Nadia; Borderies, Mary; Diaz-Schümmer, Carlos; Jamali, Maryam; Jimenez-Lluva, David; Kiefer, Joshua; Larsson, Anna; Lopez-Gilabert, Lola; Mione, Michele; Mould, Toby JD; Pavesi, Sara; Roth, Georg; Tomicic, Maja

    2017-04-01

    The terrestrial water cycle is one of many unique regulatory systems on planet Earth. It is directly responsible for sustaining biological life on land and human populations by ensuring sustained crop yields. However, this delicate balanced system continues to be influenced significantly by a changing climate, which has had drastic impacts particularly on the polar regions. Precipitation is a key process in the weather and climate system, due to its storage, transport and release of latent heat in the atmosphere. It has been extensively investigated in low latitudes, in which detailed models have been established for weather prediction. However, a gap has been left in higher latitudes above 65°, which show the strongest response to climate changes and where increasing precipitations have been foreseen in the future. In order to establish a global perspective of atmospheric processes, space observation of high-latitude areas is crucial to produce globally consistent data. The increasing demand for those data has driven a critical need to devise a mission which fills the gaps in current climate models. The authors propose the Polar Precipitation Satellite (PoPSat), an innovative satellite mission to provide enhanced observation of light and medium precipitation, focusing on snowfall and light rain in high latitudes. PoPSat is the first mission aimed to provide high resolution 3D structural information about snow and light precipitation systems and cloud structure in the covered areas. The satellite is equipped with a dual band (Ka and W band) phased-array radar. These antennas provide a horizontal resolution of 2 km and 4 km respectively which will exceed all other observations made to date at high-latitudes, while providing the additional capability to monitor snowfall. The data gathered will be compatible and complementary with measurements made during previous missions. PoPSat has been designed to fly on a sun-synchronous, dawn-dusk orbit at 460 km. This orbit

  12. Determination of 210 Po in Water%水中210Po 的分析

    Institute of Scientific and Technical Information of China (English)

    王莉莉; 张晔; 陆月萍; 周彦; 曹钟港

    2013-01-01

      水中痕量210 Po 分析采用的是示踪剂的α能谱分析法。在待分析水样中加入208 Po 示踪剂,以氢氧化铁共沉淀的形式载带钋,在0.5 mol/L 盐酸体系中利用钋对银的高度选择性实现自沉积。利用α谱仪探测系统对样品源测量48 h ,根据钋同位素的对应谱分析210 Po 活度。本文讨论该法与我国现行国标、EML 及 IAEA 分析技术的差异性。%  The determination of 210 Po in water samples was carried out by using of 208 Po tracer with the aid of alpha spectrometry .Adding 208 Po tracer to water samples before preliminary preparation ,the 210 Po and were co-precipitated with iron hydroxide .The polonium were auto-deposited on silver disc by advantage of its high selectiveness in 0 .5 mol/L hydrochloric acid solution .The sample source was counted for 60 hours in al-pha spectrometry system .The determination of 210 Po activity was performed according to different spectra .In addition ,the article discusses the differences of the present analytical method and the national standards ,EML and IAEA methods . 208 Po

  13. Scavenging and fractionation of particle-reactive radioisotopes 7Be, 210Pb and 210Po in the atmosphere

    Science.gov (United States)

    Chen, Jinfang; Luo, Shangde; Huang, Yipu

    2016-09-01

    The scavenging and fractionation of 7Be, 210Pb, and 210Po in the atmosphere are investigated by measuring their activities in rainwater collected from 68 rain events during March 2004 to April 2006 at a coastal station of Xiamen, southeastern China. In addition to documenting the large temporal variations in activities, fluxes, and isotope ratios of 7Be, 210Pb and 210Po in rainwater and the role of rainfall intensity in radionuclide scavenging, our results show that an enhanced deposition of 7Be and 210Pb occurs in the spring than in other seasons and is attributed to the "funnel effect" due to the increased atmospheric vertical convective mixing in the spring. This latter hypothesis is further supported by the observed seasonal and inter-annual variations in 7Be/210Pb and 210Po/210Pb ratios showing that the weakening of vertical convective mixing or stratosphere-troposphere exchange (STE) at the study site is linked with the enhancement of summer monsoons. It appears that the rainfall intensity, in connection with the vertical (e.g., STE) and horizontal (summer monsoons) air transport, exerts an important control on the activities, fluxes, and isotope ratios of 7Be, 210Pb, and 210Po in the atmosphere. Application of the observational data to a theoretical model shows that there are significant fractionations among 7Be, 210Pb, and 210Po in the atmosphere, with the scavenging rate constant or reciprocal of the residence time of radionuclide in the atmosphere being 210Pb > 7Be > 210Po. A revised Poet et al. (1972)'s method is proposed for quantitative constraint on the scavenging behavior of radionuclide, aerosols, and aerosol-associated trace pollutants in the atmosphere.

  14. New NaSrPO$_4$:Sm$^{3+}$ phosphor as orange-red emitting material

    Indian Academy of Sciences (India)

    KUN-HSIEN CHEN; MIN-HANG WENG; RU-YUAN YANG; CHENG-TANG PAN

    2016-09-01

    Sm$^{3+}$-activated NaSrPO4 phosphors could be efficiently excited at 403 nm, and exhibited a bright red emission mainly including four wavelength peaks of 565, 600, 646 and 710 nm. The highest emission intensity was foundfor NaSr$_{1−x}$PO$_{4}$:$x$Sm$^{3+}$ with a composition of $x = 0.007$. Concentration quenching was observed as the composition of $x$ exceeds 0.007. The decay time values of NaSr1−xPO4:xSm3+ phosphors range from around 2.55 to 3.49 ms. NaSr$_{1−x}$PO$_{4}$:$x$Sm$^{3+}$ phosphor shows a higher thermally stable luminescence and its thermal quenching temperature$T_{50}$ was found to be 350$^{\\circ}$C, which is higher than that of commercial YAG:Ce$^{3+}$ phosphor and ZnS:(Al, Ag) phosphor. Because NaSr$_{1−x}$PO$_{4}$:$x$Sm$^{3+}$ phosphor features a high colour-rendering index and chemical stability, it is potentially useful as a new scintillation material for white light-emitting diodes.

  15. Controlled synthesis, characterization and photocatalytic activity of BiPO4 nanostructures with different morphologies

    Science.gov (United States)

    Cheng, Lang-Wei; Tsai, Jui-Chien; Huang, Tzu-Yun; Huang, Chang-Wei; Unnikrishnan, Binesh; Lin, Yang-Wei

    2014-04-01

    The synthesis of bismuth phosphate (BiPO4) nanostructures with various morphologies and phases was explored under ultrasound irradiation and hydrothermal process. Powder x-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and UV-Vis diffuse reflectance spectroscopy (DRS) were used to characterize the BiPO4 samples. The effects of ultrasound irradiation and hydrothermal conditions on the phases and morphologies of the BiPO4 samples were studied, and the growth mechanisms of the 1D structure were investigated. The different BiPO4 samples exhibited different optical properties and photocatalytic activities for the degradation of methyl blue (MB) under UV light irradiation. The experimental results suggest that the high photocatalytic activity of the sample prepared under hydrothermal conditions is due to a low electron and hole recombination rate and the high potential of the photogenerated holes in the valence band. The practicality of this BiPO4 photocatalyst was validated for the degradation of MB in environmental and industrial wastewater samples, which demonstrated the advantages of its high photocatalytic activity.

  16. Laser isotope separation by multiple photon absorption

    Science.gov (United States)

    Robinson, C.P.; Rockwood, S.D.; Jensen, R.J.; Lyman, J.L.; Aldridge, J.P. III.

    1987-04-07

    Multiple photon absorption from an intense beam of infrared laser light may be used to induce selective chemical reactions in molecular species which result in isotope separation or enrichment. The molecular species must have a sufficient density of vibrational states in its vibrational manifold that, is the presence of sufficiently intense infrared laser light tuned to selectively excite only those molecules containing a particular isotope, multiple photon absorption can occur. By this technique, for example, intense CO[sub 2] laser light may be used to highly enrich [sup 34]S in natural SF[sub 6] and [sup 11]B in natural BCl[sub 3]. 8 figs.

  17. High efficient multifunctional Ag{sub 3}PO{sub 4} loaded hydroxyapatite nanowires for water treatment

    Energy Technology Data Exchange (ETDEWEB)

    Li, Yaling; Zhou, Hangyu; Zhu, Genxing [Center for Biomaterials and Biopathways, Department of Chemistry, Zhejiang University, Hangzhou (China); Shao, Changyu; Pan, Haihua; Xu, Xurong [Center for Biomaterials and Biopathways, Department of Chemistry, Zhejiang University, Hangzhou (China); Qiushi Academy for Advanced Studies, Zhejiang University (China); Tang, Ruikang, E-mail: rtang@zju.edu.cn [Center for Biomaterials and Biopathways, Department of Chemistry, Zhejiang University, Hangzhou (China); Qiushi Academy for Advanced Studies, Zhejiang University (China)

    2015-12-15

    Highlights: • The multifunctional Ag{sub 3}PO{sub 4} loaded hydroxyapatite (HAP) nanowires were synthesized via a facile in-situ precipitation method. • By optimizing the initial concentration of AgNO{sub 3}, the well-distributed Ag{sub 3}PO{sub 4}/HAP composites could be achieved. • The Ag{sub 3}PO{sub 4}/HAP composites showed excellent photocatalytic performance for the decomposition of dyes under visible light irradiation. • The maximum absorption capacity of the Ag{sub 3}PO{sub 4}/HAP composites for Pb(II) was 250 mg/g, approximately three times as that of pure HAP. • The Ag{sub 3}PO{sub 4}/HAP composites also exhibited excellent antibacterial activities even at relative low concentrations. - Abstract: Organic, inorganic, and biological pollutants are typical water contaminants and they seriously affect water quality. In this study, we suggested that a novel multifunctional Ag{sub 3}PO{sub 4} loaded hydroxyapatite (HAP) material can remove the typical pollutants from water. The Ag{sub 3}PO{sub 4}/HAP composites were synthesized facilely via in-situ precipitation of Ag{sub 3}PO{sub 4} on the pre-existing HAP nanowires. By optimizing the composition of Ag{sub 3}PO{sub 4} and HAP, the material could achieve an optimal photocatalytic activity to decompose rhodamine B (RhB), methyl orange (MO) and methylene blue (MB) under visible light irradiations with enhanced pH stability. Besides, the adsorption of Pb(II) on the Ag{sub 3}PO{sub 4}/HAP reached a maximum capacity of 250 mg/g and this value was approximately three times as that of pure HAP. Furthermore, the composite material exhibited excellent antibacterial activities towards gram-negative bacterium (Escherichia coli) and gram-positive bacterium (Stphylococcus aureus). The results highlighted the cooperative effect between Ag{sub 3}PO{sub 4} and hydroxyapatite (HAP). The simultaneous removals of dyes, toxic metal ions, and bacteria with a high efficiency followed an easy approach for the purification

  18. An improved stable isotope N-terminal labeling approach with light/heavy TMPP to automate proteogenomics data validation: dN-TOP.

    Science.gov (United States)

    Bertaccini, Diego; Vaca, Sebastian; Carapito, Christine; Arsène-Ploetze, Florence; Van Dorsselaer, Alain; Schaeffer-Reiss, Christine

    2013-06-07

    In silico gene prediction has proven to be prone to errors, especially regarding precise localization of start codons that spread in subsequent biological studies. Therefore, the high throughput characterization of protein N-termini is becoming an emerging challenge in the proteomics and especially proteogenomics fields. The trimethoxyphenyl phosphonium (TMPP) labeling approach (N-TOP) is an efficient N-terminomic approach that allows the characterization of both N-terminal and internal peptides in a single experiment. Due to its permanent positive charge, TMPP labeling strongly affects MS/MS fragmentation resulting in unadapted scoring of TMPP-derivatized peptide spectra by classical search engines. This behavior has led to difficulties in validating TMPP-derivatized peptide identifications with usual score filtering and thus to low/underestimated numbers of identified N-termini. We present herein a new strategy (dN-TOP) that overwhelmed the previous limitation allowing a confident and automated N-terminal peptide validation thanks to a combined labeling with light and heavy TMPP reagents. We show how this double labeling allows increasing the number of validated N-terminal peptides. This strategy represents a considerable improvement to the well-established N-TOP method with an enhanced and accelerated data processing making it now fully compatible with high-throughput proteogenomics studies.

  19. 新的大功率PoE标准——PoE+

    Institute of Scientific and Technical Information of China (English)

    Clay Stanford

    2009-01-01

    @@ 以太网供电(PoE)标准由IEEE 802.3af任务组于2003年制定,并已被业界所广泛接受.目前,各家主要的制造商均可提供具PoE端口的网络交换机.IP电话一直是PoE普及的推动力,不过PoE也广泛应用于其他多种应用,如无线接入点(WAP)、保安摄像机、RFID标签阅读器等,以及用来为出口标志,甚至电吉他等不那么主流的应用供电.

  20. A novel methodology to investigate isotopic biosignatures

    Science.gov (United States)

    Horner, T. J.; Lee, R. B. Y.; Henderson, G. M.; Rickaby, R. E. M.

    2012-04-01

    An enduring goal of trace metal isotopic studies of Earth History is to find isotopic 'fingerprints' of life or of life's individual physiochemical processes. Generally, such signatures are sought by relating an isotopic effect observed in controlled laboratory conditions or a well-characterized environment to a more complex system or the geological record. However, such an approach is ultimately limited because life exerts numerous isotopic fractionations on any one element so it is hard to dissect the resultant net fractionation into its individual components. Further, different organisms, often with the same apparent cellular function, can express different isotopic fractionation factors. We have used a novel method to investigate the isotopic fractionation associated with a single physiological process-enzyme specific isotopic fractionation. We selected Cd isotopes since only one biological use of Cd is known, CdCA (a Cd/Zn carbonic anhydrase from the coastal diatom T. Weissflogii). Thus, our investigation can also inform the long standing mystery as to why this generally toxic element appears to have a nutrient-like dissolved isotopic and concentration profile in the oceans. We used the pET-15b plasmid to insert the CdCA gene into the E. coli genome. There is no known biochemical function for Cd in E. coli, making it an ideal vector for studying distinct physiological processes within a single organism. The uptake of Cd and associated isotopic fractionation was determined for both normal cells and those expressing CdCA. It was found that whole cells always exhibited a preference for the light isotopes of Cd, regardless of the expression of CdCA; adsorption of Cd to cell surfaces was not seen to cause isotopic fractionation. However, the cleaning procedure employed exerted a strong control on the observed isotopic composition of cells. Using existing protein purification techniques, we measured the Cd isotopic composition of different subcellular fractions of E

  1. Electronic Properties of LiFePO4 and Li doped LiFePO4

    Energy Technology Data Exchange (ETDEWEB)

    Allen, J.L.; Zhuang, G.V.; Ross, P.N.; Guo, J.-H.; Jow, T.R.

    2006-05-31

    LiFePO{sub 4} has several potential advantages in comparison to the transition metal oxide cathode materials used in commercial lithium-ion batteries. However, its low intrinsic electronic conductivity ({approx} 10{sup -9} S/cm) is problematic. We report here a study by soft x-ray absorption/emission spectroscopy of the electronic properties of undoped LiFePO{sub 4} and Li-doped LiFePO{sub 4} in which Li{sup +} ions are substituted for Fe{sup 2+} ions in an attempt to increase the intrinsic electronic conductivity. The conductivities of the Li{sub 1+x}Fe{sub 1-x}PO{sub 4} samples were, however, essentially unchanged from that of the undoped LiFePO{sub 4}. Nonetheless, evidence for changing the electronic properties of LiFePO{sub 4} by doping with excess Li+ was observed by the XAS/XES spectroscopy. New pre-edge features the O-1s XAS spectrum of Li{sub 1.05}Fe{sub 0.95}PO4 is a direct indication that the charge compensation for substitution of Fe{sup 2+} by Li{sup +} resides in the unoccupied O-2p orbitals. A charge transfer (CT) excitation was also observed in the doped material implying that the unoccupied O-2p orbitals created by doping are strongly hybridized with unoccupied Fe-3d orbitals of neighboring sites. However, the strong covalent bonding within the (PO{sub 4}){sup 3-} anions and the large separation of the Fe cations means that the charge created by doping is not delocalized in the manner of electrons or holes in a semiconductor.

  2. A PoE (Power over Ethernet) Switching Power%PoE开关电源

    Institute of Scientific and Technical Information of China (English)

    王智剑; 杨宇航

    2005-01-01

    文中对IEEE802.3af标准做介绍,阐述符合该标准的PoE开关电源的设计方案及其实现.尽管该电源专门设计用于VoIP电话,但其本质上具有一般性,只需简单的调整即可用于其它的PoE应用.

  3. Early onset of deformation in the neutron-deficient polonium isotopes

    Science.gov (United States)

    Cocolios, T. E.; Andreyev, A. N.; Antalic, S.; Barzakh, A. E.; Bastin, B.; Büscher, J.; Darby, I. G.; Dexters, W.; Fedorov, D. V.; Fedosseev, V. N.; Flanagan, K. T.; Franchoo, S.; Fritzsche, S.; Huber, G.; Huyse, M.; Keupers, M.; Köster, U.; Kudryavtsev, Yu; Mané, E.; Marsh, B. A.; Molkanov, P. L.; Page, R. D.; Seliverstov, M. D.; Sjödin, A. M.; Stefan, I.; Van de Walle, J.; Van Duppen, P.; Venhart, M.; Zemlyanoy, S. G.

    2012-09-01

    In-source laser spectroscopy has been performed at CERN-ISOLDE with the RILIS laser ion source on 191-204,206,208-211,216,218Po. New information on the β decay of 199Po were extracted in the process, challenging previous results. Large-scale atomic calculations were performed to extract the changes in the mean-square charge radius δlangler2rangle from the isotope shifts. The δlangler2rangle for the even-A isotopes reveal a large deviation from the spherical droplet model for N < 116.

  4. Physical Oceanography Distributed Active Archive Center (PO.DAAC)

    Data.gov (United States)

    National Aeronautics and Space Administration — PO.DAAC is an element of the Earth Observing System Data Information System (EOSDIS). PO.DAAC's primary responsibility is to provide distribution and archive support...

  5. Fabrication of Z-scheme Ag3PO4/MoS2 composites with enhanced photocatalytic activity and stability for organic pollutant degradation

    Science.gov (United States)

    Zhu, Chaosheng; Zhang, Lu; Jiang, Bo; Zheng, Jingtang; Hu, Ping; Li, Sujuan; Wu, Mingbo; Wu, Wenting

    2016-07-01

    In this study, highly efficient visible-light-driven Ag3PO4/MoS2 composite photocatalysts with different weight ratios of MoS2 were prepared via the ethanol-water mixed solvents precipitation method and characterized by ICP, XRD, HRTEM, FE-SEM, BET, XPS, UV-vis DRS and PL analysis. Under visible-light irradiation, Ag3PO4/MoS2 composites exhibit excellent photocatalytic activity towards the degradation of organic pollutants in aqueous solution. The optimal composite with 0.648 wt% MoS2 content exhibits the highest photocatalytic activity, which can degrade almost all MB under visible-light irradiation within 60 min. Recycling experiments confirmed that the Ag3PO4/MoS2 catalysts had superior cycle performance and stability. The photocatalytic activity enhancement of Ag3PO4/MoS2 photocatalysts can be mainly ascribed to the efficient separation of photogenerated charge carriers and the stronger oxidation and reduction ability through a Z-scheme system composed of Ag3PO4, Ag and MoS2, in which Ag particles act as the charge separation center. The high photocatalytic stability is due to the successful inhibition of the photocorrosion of Ag3PO4 by transferring the photogenerated electrons of Ag3PO4 to MoS2. The evidence of the Z-scheme photocatalytic mechanism of the composite photocatalysts could be obtained from the active species trapping experiments and the photoluminescence technique.

  6. Stable isotope studies

    Energy Technology Data Exchange (ETDEWEB)

    Ishida, T.

    1992-01-01

    The research has been in four general areas: (1) correlation of isotope effects with molecular forces and molecular structures, (2) correlation of zero-point energy and its isotope effects with molecular structure and molecular forces, (3) vapor pressure isotope effects, and (4) fractionation of stable isotopes. 73 refs, 38 figs, 29 tabs.

  7. Informatique et poésie

    OpenAIRE

    Vuillemin, Alain

    1995-01-01

    Sommaire du numéro :http://archive-edutice.ccsd.cnrs.fr/edutice-00000865; Un écran s'allume, des caractères jaillissent, des lettres surgissent, des mots scintillent, des phrases s'animent, des vers s'assemblent, des formes s'élaborent, des symboles prennent vie, un sens naît. Une sorte de miracle paraît s'être produit : un texte s'est construit, un souffle a passé, un poème s'est « généré ». Un acte de création poétique a eu lieu grâce à l'aide d'un ordinateur. Deux revues, Alire depuis 1989...

  8. Aspects on the analysis of 210Po

    DEFF Research Database (Denmark)

    Henricsson, F.; Ranebo, Y.; Holm, E.

    2011-01-01

    will be too low. Both these systematic errors give rise to a too high 210Po/210Pb ratio. The fraction of 210Pb which is plating out has been assessed in this study for different matrices and is about 50–90%. During the measurement by solid state Si-detectors, some Po is evaporated in the vacuum conditions......-ashing by the use of a double-tracer technique. We have found that the losses were about 30% when open glass beakers were used and about 17% when the samples were digested in microwave oven. When long-necked bottles (Kjeldahl flasks) were used, a loss of about 20% was registered. It has also been observed that 210...

  9. The BiPo-3 detector.

    Science.gov (United States)

    Loaiza, P; Barabash, A S; Basharina-Freshville, A; Birdsall, E; Blondel, S; Blot, S; Bongrand, M; Boursette, D; Brudanin, V; Busto, J; Caffrey, A J; Calvez, S; Cascella, M; Cerna, C; Chauveau, E; Chopra, A; Capua, S De; Duchesneau, D; Durand, D; Egorov, V; Eurin, G; Evans, J J; Fajt, L; Filosofov, D; Flack, R; Garrido, X; Gómez, H; Guillon, B; Guzowski, P; Holý, K; Hodák, R; Huber, A; Hugon, C; Jeremie, A; Jullian, S; Kauer, M; Klimenko, A; Kochetov, O; Konovalov, S I; Kovalenko, V; Lang, K; Lemière, Y; Noblet, T Le; Liptak, Z; Liu, X R; Lutter, G; Macko, M; Mamedov, F; Marquet, C; Mauger, F; Morgan, B; Mott, J; Nemchenok, I; Nomachi, M; Nova, F; Ohsumi, H; Oliviéro, G; Pahlka, R B; Pater, J; Perrot, F; Piquemal, F; Povinec, P; Přidal, P; Ramachers, Y A; Remoto, A; Richards, B; Riddle, C L; Rukhadze, E; Saakyan, R; Sarazin, X; Shitov, Yu; Simard, L; Šimkovic, F; Smetana, A; Smolek, K; Smolnikov, A; Söldner-Rembold, S; Soulé, B; Štekl, I; Thomas, J; Timkin, V; Torre, S; Tretyak, Vl I; Tretyak, V I; Umatov, V I; Vilela, C; Vorobel, V; Waters, D; Žukauskas, A

    2017-05-01

    The BiPo-3 detector is a low radioactive detector dedicated to measuring ultra-low natural contaminations of (208)Tl and (214)Bi in thin materials, initially developed to measure the radiopurity of the double β decay source foils of the SuperNEMO experiment at the μBq/kg level. The BiPo-3 technique consists in installing the foil of interest between two thin ultra-radiopure scintillators coupled to low radioactive photomultipliers. The design and performances of the detector are presented. In this paper, the final results of the (208)Tl and (214)Bi activity measurements of the first enriched (82)Se foils are reported for the first time, showing the capability of the detector to reach sensitivities in the range of some μBq/kg. Copyright © 2017 Elsevier Ltd. All rights reserved.

  10. Research on high rate capabilities B-substituted LiFePO4.

    Science.gov (United States)

    Wang, Fu; Zhang, Yun; Chen, Chao

    2013-02-01

    LiFePO4 is currently recognized as one of the most promising electrode materials for large-scale application of lithium ion batteries. However, the limitation of rate capability is believed to be intrinsic to this family of compounds due to the existence of larger tetrahedral (PO4)3- unit and quasi-hexagonal close-packed oxygen array. This paper report here a systematic investigation of the enhancement of rate performance by partly substitution of light small triangle oxyanion, (BO3)3-, for the larger tetrahedral (PO4)3- units in LiFePO4. Cathode electrode materials LiFeB(x)P(1_x)O(4-delta), in which X = 0, 3, 6 and 9, mol%, were synthesized by solid-state method. The as-synthesized products were characterized by X-Ray Diffraction (XRD), Scanning Electron Microscope (SEM) and Electrochemical Measurements. The results showed that 6 mol% of boron substitution had no effect on the structure of LiFePO4 material, but significantly improved its rate performance. The initial discharge capacity of the LiFeB0.06P0.94O(4-delta) sample was 145.62 mAh/g at 0.1 C, and the capacity retention ratios of 81% at 2 C and 76% at 5 C were obtained, demonstrating that a proper amount of boron substitution (lower than 6 mol%) could significantly improve the rate performance of LiFePO4 cathode material.

  11. Silicon isotope fractionation during magmatic differentiation

    Science.gov (United States)

    Savage, Paul S.; Georg, R. Bastian; Williams, Helen M.; Burton, Kevin W.; Halliday, Alex N.

    2011-10-01

    The Si isotopic composition of Earth's mantle is thought to be homogeneous (δ 30Si = -0.29 ± 0.08‰, 2 s.d.) and not greatly affected by partial melting and recycling. Previous analyses of evolved igneous material indicate that such rocks are isotopically heavy relative to the mantle. To understand this variation, it is necessary to investigate the degree of Si isotopic fractionation that takes place during magmatic differentiation. Here we report Si isotopic compositions of lavas from Hekla volcano, Iceland, which has formed in a region devoid of old, geochemically diverse crust. We show that Si isotopic composition varies linearly as a function of silica content, with more differentiated rocks possessing heavier isotopic compositions. Data for samples from the Afar Rift Zone, as well as various igneous USGS standards are collinear with the Hekla trend, providing evidence of a fundamental relationship between magmatic differentiation and Si isotopes. The effect of fractionation has been tested by studying cumulates from the Skaergaard Complex, which show that olivine and pyroxene are isotopically light, and plagioclase heavy, relative to the Si isotopic composition of the Earth's mantle. Therefore, Si isotopes can be utilised to model the competing effects of mafic and felsic mineral fractionation in evolving silicate liquids and cumulates. At an average SiO 2 content of ˜60 wt.%, the predicted δ 30Si value of the continental crust that should result from magmatic fractionation alone is -0.23 ± 0.05‰ (2 s.e.), barely heavier than the mantle. This is, at most, a maximum estimate, as this does not take into account weathered material whose formation drives the products toward lighter δ 30Si values. Mass balance calculations suggest that removal of continental crust of this composition from the upper mantle will not affect the Si isotopic composition of the mantle.

  12. Determination of (210)Po and uranium in high salinity water samples.

    Science.gov (United States)

    Grabowski, Paweł; Bem, Henryk

    A method for the determination of uranium and (210)Po in high salinity water samples has been elaborated. Both radionuclides are preconcentrated from 0.5 dm(3) saline media by co-precipitation with hydrated manganese dioxide, followed by dissolution of the precipitate in 200 mL of 1 M HCl. Uranium isotopes (235)U and (238)U can be directly determined by ICP MS method with a detection limit of 0.01 ppb for (238)U. Prior to a selective determination of (210)Po, the majority of other naturally occurring α-emitting radionuclides (uranium, thorium and protactinium) can be stripped from this solution by their extraction with a 50% solution of HDEHP in toluene. Finally, (210)Po is simply separated by direct transfer to an extractive scintillator containing 5% of trioctylphosphine oxide in Ultima Gold F cocktail and determined by an α/β separation liquid scintillation technique with detection limit below 0.1 mBq/dm(3).

  13. Razmjena poštanskih pošiljaka Jugoslavije sa svijetom u 1979-1988.

    Directory of Open Access Journals (Sweden)

    Slavko Jaram

    2012-10-01

    Full Text Available U ovom radu je analizirana i ocijenjena međunarodna razmjena poštanskih pošiljaka Jugoslavijesa svijetom u razdoblju 1979-1988.Zaključuje se o snazi, smjeru i značajkama nastalih promjena u dinamici i strukturi, posebnoza svaku skupinu usluga (pismovne i paketske. Pismovne i paketske usluge pokazuju stalno smanjenje u oba smjera (izvoz i uvoz začitavo razdoblje. Analitičke slike geografskedistribucije usluga pokazuju dominantnu uloguzemalja Evrope, posebno SR Njemačke.Zaključuje se da je ovakav pad međunarodnoga poštanskog prometa, uzrokovan izrazitom razvojnom tendencijom supstitucija među pojedinim vrstama usluga u uvjetima širenja. suvremene telekomunikacijske mr:eže, iako se ne bi smjeli zanemariti ni drugi uzroci, posebno u paketskih pošiljaka, koji su proizlazili iz opće ekonomske situacije zemlje u osamdesetim godinama ovog stoljeća.U budućnosti valja očekivati dugoročniju stagnaciju međunarodne razmjene poštanskih usluga, a u nekih usluga i nastavak opadanja.

  14. Forenzika elektronske pošte

    Directory of Open Access Journals (Sweden)

    Milorad S. Markagić

    2013-10-01

    Full Text Available U najopštijem smislu digitalna forenzika može se definisati kao skup metoda za prikupljanje, analizu i prezentaciju digitalnih dokaza koji se mogu pronaći na računarima, serverima, u računarskim mrežama, bazama podataka, mobilnim uređajima i svim drugim elektronskim uređajima na kojima se čuvaju podaci. U ovom radu su opisane metode prikupljanja digitalnih dokaza u elektronskoj pošti i njihova analiza. Uvod Elektronska pošta se kao dokazni materijal pojavljuje u velikom broju kako građanskih tako i kriminalnih forenzičkih istraga. Elektronska pošta i elektronska pošta zasnovana na internet serverima  širi se veoma brzo, pa lako i brzo završi i na računaru korisnika kome nije namenjena. Prvu elektronsku poruku poslao je Ray Tomilson 1971. godine, a deset godina kasnije u kombinaciji sa personalnim računarima i internetom prerasta u globalni način komuniciranja i personalnog i poslovnog. Takođe se koristi i u svrhu zabave, načina razmene podataka, ali predstavlja i nezamenjiv izvor digitalnih dokaza, kada dodje do računarskog incidenta. Analiza elektronske pošte Svaka elektronska poruka sastoji se od dva dela: zaglavlja i teksta poruke. Iz zaglavlja je moguće saznati izvorišnu i odredišnu adresu, pošiljaoca i namenjenog primaoca, a telo poruke sadrži tekst poruke. Ekstenzije dokumenata elektronske pošte U slučajevima kada je potrebno otkriti samo dokumente potrebne za pregled elektronskih poruka, ili kopirati pojedinačni dokument sačuvan unutar elektronske pošte, moguće je koristiti sistem na istraživanom računaru ili specijalizovani softver kao što je Outlook Extract Pro ili Outlook Export. Mnogo ispravniji, sigurniji i jednostavniji način je korišćenje forenzičkih alata kao što su EnCase ili FTK, sa ugrađenim pregledačima koji omogućavaju pregled i snimanje sadržaja baze podataka kao i njihovo kopiranje na druge medije za dalju analizu. Forenzički alati automatizuju proces skidanja i kopiranja

  15. Eu3+-doped LaPO4 and LaAlO3 nanosystems and their luminescence properties

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    Eu3+ ion-doped LaPO4 nanowires or nanorods have been successfully synthesized by a simple hydrothermal method.The influence of varying the hydrothermal and subsequent sintering conditions on the morphology and structure of the LaPO4 host has been investigated by scanning electron microscopy(SEM) and X-ray diffraction(XRD).For comparison,the Eu3+ ions were also doped into monoclinic monazite LaPO4 nanoparticles and perovskite LaAlO3 nanoparticles.The relative intensities of the emission lines of the LaPO4:Eu3+ nanosystems were essentially independent of their shape.The optimal doping concentrations in the monoclinic LaPO4 and perovskite LaAlO3 nanosystems were determined to be about 5.0 and 3.5 mol%,respectively.Under appropriate UV-radiation,the red light emitted from LaAlO3:Eu3+(3.5 mol%) was brighter than that from LaPO4:Eu3+(5.0 mol%) nanomaterial,resulting from differences in their spin-orbit couplings and covalence,which indicates that the nanoscale LaAlO3 is a promising host material for rare earth ions.

  16. Eu3+-doped LaPO4 and LaAlO3 nanosystems and their luminescence properties

    Institute of Scientific and Technical Information of China (English)

    WAN Qiang; HE YuPing; DAI Ning; ZOU BingSuo

    2009-01-01

    Eu3+ Ion-dolpod LaPO4 nanowires or nanorods have been successfully synthesized by a simple hydrothermal method.The influence of varying the hydrothermal and subsequent sintering conditions on the morphology and structure of the LaPO4 host has been investigated by scanning electron microscopy(SEM)and X-ray diffraction(XRD).For comparison,the Eu3+ ions were also doped into monoclinic monazite LaPO4 nanoparticles and perovskite LaAlO3 nanoparticles.The relative intensities of the emission lines of the LaPO4:Eu3+ nanosystems were essentially independent of their shape.The optimal doping concentrations in the monoclinic LaPO4 and perovskite LaAlO3 nanosystems were determined to be about 5.0 and 3.5 mol%,respectively.Under appropriate UV-radiation,the red light emitted from LaAlO3:Eu3+(3.5 mol%)was brighter than that from LaPO4:Eu3+(5.0 mol%)nanomaterial,resulting from differences in their spin-orbit couplings and covalence,which indicates that the nanoscale LaAlO3 is a promising host material for rare earth ions.

  17. Chromium Isotopes in Carbonate Rocks: New Insights into Proterozoic Atmospheric Oxygenation

    Science.gov (United States)

    Kah, L. C.; Gilleaudeau, G. J.; Frei, R.; Kaufman, A. J.; Azmy, K.; Bartley, J. K.; Chernyavskiy, P.; Knoll, A. H.

    2015-12-01

    There has been a long-standing debate in geobiology about the role that Earth's oxygenation played in the evolution of complex life. Temporal linkages exist between the Great Oxidation Event (GOE) and the evolution of eukaryotes, as well as Neoproterozoic rise in oxygen and the diversification of metazoans. Further advances have been hampered, however, by the lack of direct proxies that mark specific levels of atmospheric pO2 in the geologic past. Chromium (Cr) isotopes show promise in this regard because the oxidation of Cr during terrestrial weathering—which results in isotopic fractionation—is dependent on a specific threshold of atmospheric pO2 (0.1-1% of the present atmospheric level [PAL]). This threshold value broadly coincides with recent estimates of the oxygen requirements of early animals. Here we report new Cr-isotope data from four late Mesoproterozoic carbonate-dominated successions. Samples were collected from the Turukhansk Uplift (Siberia), the El Mreiti Group (Mauritania), the Vazante Group (Brazil), and the Angmaat Formation (Canada). We emphasize the application of Cr-isotopes to carbonate rocks because the broad temporal range of this lithology in the geologic record provides an opportunity to significantly expand our understanding of Proterozoic oxygenation on shorter time scales. Our data indicate that pO2 levels required to support early animals were attained long before Neoproterozoic metazoan diversification, although the large degree of isotopic heterogeneity in our dataset may indicate that pO2 > 0.1-1% PAL was only a transient phenomenon in the Mesoproterozoic. This study demonstrates the utility of Cr-isotopes as an atmospheric redox proxy in carbonate rocks and helps inform future avenues of research on Proterozoic pO2 thresholds.

  18. Calcium isotopes in wine

    Science.gov (United States)

    Holmden, C. E.

    2011-12-01

    Merlot grapes was -1.94%, which is lower than any of the bottled wines measured, thus far, whether white or red. The wine made from this juice yielded -1.16%, which points to fermentation being the principal source of isotopic variability found in bottled wine. The working hypothesis is that light isotopes of Ca are preferentially stripped from the juice during maceration, fermentation, and lees contact, by ion exchange sites on solid organic-matter comprising the skins and yeast and/or by Ca-tartrate precipitation. High quality wines (especially reds) tend to involve longer contact times between juice and skins in order to increase the extraction of color and phenolic compounds (tannins) from the grape skins, a practice that might also result in greater losses of light isotopes of Ca from the juice, thus explaining the isotopic pattern in bottled wine.

  19. Isotopically Modified Molybdenum: Production for Application in Nuclear Energy

    Science.gov (United States)

    Smirnov, A. Yu.; Bonarev, A. K.; Sulaberidze, G. A.; Borisevich, V. D.; Kulikov, G. G.; Shmelev, A. N.

    The possibility to use the isotopically modified molybdenum as a constructive material for the fuel rods of light water and fast reactors is discussed. The calculations demonstrate that the isotopically modified molybdenum with an average neutron absorption cross-section comparable to that of zirconium can be obtained with the reasonable for practice cost by a cascade of gas centrifuges, specially designed for separation of non-uranium isotopes.

  20. Pristine extraterrestrial material with unprecedented nitrogen isotopic variation.

    Science.gov (United States)

    Briani, Giacomo; Gounelle, Matthieu; Marrocchi, Yves; Mostefaoui, Smail; Leroux, Hugues; Quirico, Eric; Meibom, Anders

    2009-06-30

    Pristine meteoritic materials carry light element isotopic fractionations that constrain physiochemical conditions during solar system formation. Here we report the discovery of a unique xenolith in the metal-rich chondrite Isheyevo. Its fine-grained, highly pristine mineralogy has similarity with interplanetary dust particles (IDPs), but the volume of the xenolith is more than 30,000 times that of a typical IDP. Furthermore, an extreme continuum of N isotopic variation is present in this xenolith: from very light N isotopic composition (delta(15)N(AIR) = -310 +/- 20 per thousand), similar to that inferred for the solar nebula, to the heaviest ratios measured in any solar system material (delta(15)N(AIR) = 4,900 +/- 300 per thousand). At the same time, its hydrogen and carbon isotopic compositions exhibit very little variation. This object poses serious challenges for existing models for the origin of light element isotopic anomalies.

  1. Improved photoelectrochemical performance of Z-scheme g-C3N4/Bi2O3/BiPO4 heterostructure and degradation property

    Science.gov (United States)

    Li, Junqi; Yuan, Huan; Zhu, Zhenfeng

    2016-11-01

    In g-C3N4/Bi2O3/BiPO4, the p-n junction between p-type Bi2O3 and n-type BiPO4 was encapsulated by g-C3N4 and a direct Z-scheme was built between g-C3N4 and Bi2O3. The optical, morphological and photoelectrochemical (PEC) properties of BiPO4, g-C3N4/BiPO4, Bi2O3/BiPO4 and g-C3N4/Bi2O3/BiPO4 hierarchical Z-scheme system were studied. More than 90% photodegradation of methyl orange (MO) with the exposure of simulated solar light was achieved within 160 min with the g-C3N4/Bi2O3/BiPO4, which displayed remarkably promoted photocatalytic activities than other samples. The electrochemical impedance spectra and photocurrent results also proved that efficient charge separation and better electron transport properties were achieved by g-C3N4/Bi2O3/BiPO4. In general, the addition of g-C3N4 can guide the residual electrons on p-type Bi2O3 to recombine with photoholes of g-C3N4 and make sure the left carries exhibit stronger oxidation and reduction ability to boost the production of active groups.

  2. Oxygen Isotope Signatures of UV Oxidation of Phosphite: Implications for a Biomarker in the Search for Life

    Science.gov (United States)

    Chang, S.; Blake, R.

    2013-12-01

    On the present Earth, phosphorus (P) occurs primarily in fully-oxidized form (P5+) as orthophosphate (PO4), and PO4 derived from igneous apatite minerals is considered as the primary source of P for prebiotic reactions and evolution of first life. Recent discoveries have shown, however, that abundant P compounds with valence aqueous weathering of phosphides in meteorites(1) and of fulgurites formed by lightning strikes or high-energy impacts(2). These studies concluded that PO3 was likely abundant on the oxygen-free early Earth and extraterrestrial environments, and was possibly the first form of biologically-available P, due to its greater solubility and reactivity relative to PO4 and apatite(1). These findings suggest alternative prebiotic P reservoirs to igneous apatite that would also likely have very different prebiotic/baseline PO4 δ18O values. Here we report results of experimental studies to determine the O-isotope signature of PO4 derived from PO3 oxidation catalyzed by ultraviolet (UV) radiation, which was not blocked on early Earth due to lack of an ozone layer(3). These studies are critical for interpretation of PO4 δ18O biosignatures preserved in ancient terrestrial and extraterrestrial samples. Experiments on UV-catalyzed oxidation of aqueous PO3 to PO4 were conducted using δ18O-labled PO3 and different δ18O-labled waters to gain information on (i) the source(s) of O involved and mechanism of oxidation of PO3 to PO4, and (ii) fractionations accompanying O incorporation into product PO4. Our preliminary results under modern atmospheric conditions indicate incorporation of ca. 15 % O from ambient water and ca. 10 % atmospheric O (δ18O: ~23.5 ‰) into product PO4 with a fractionation between incorporated water O and ambient water O of -20 × 4 ‰ (1 SD), assuming 75 % inheritance of O from PO3 and direct incorporation of atmospheric O into product PO4 without fractionation. If initial δ18O values of PO3 sources were the same as igneous apatite (6

  3. Online stable carbon isotope ratio measurement in formic acid, acetic acid, methanol and ethanol in water by high performance liquid chromatography-isotope ratio mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Tagami, Keiko [National Institute of Radiological Sciences, 4-9-1, Anagawa, Inage-ku, Chiba 263-8555 (Japan)], E-mail: k_tagami@nirs.go.jp; Uchida, Shigeo [National Institute of Radiological Sciences, 4-9-1, Anagawa, Inage-ku, Chiba 263-8555 (Japan)

    2008-05-05

    A suitable analysis condition was determined for high performance liquid chromatography-isotope ratio mass spectrometry (HPLC-IRMS) while making sequential measurements of stable carbon isotope ratios of {delta}{sup 13}C in formic acid, acetic acid, methanol and ethanol dissolved in water. For this online column separation method, organic reagents are not applicable due to carbon contamination; thus, water and KH{sub 2}PO{sub 4} at low concentrations were tested as mobile phase in combination with a HyPURITY AQUASTAR{sup TM} column. Formic acid, acetic acid, methanol and ethanol were separated when 2 mM KH{sub 2}PO{sub 4} aqueous solution was used. Under the determined analysis condition for HPLC-IRMS, carbon concentrations could be measured quantitatively as well as carbon isotope ratio when carbon concentration was higher than 0.4 mM L for each chemical.

  4. Uranium isotopes distinguish two geochemically distinct stages during the later Cambrian SPICE event

    DEFF Research Database (Denmark)

    Dahl, Tais Wittchen; Boyle, Richard A.; Canfield, Donald E.

    2014-01-01

    Anoxic marine zones were common in early Paleozoic oceans (542-400 Ma), and present a potential link to atmospheric pO2 via feedbacks linking global marine phosphorous recycling, primary production and organic carbon burial. Uranium (U) isotopes in carbonate rocks track the extent of ocean anoxia...

  5. Deformation and mixing of coexisting shapes in neutron-deficient polonium isotopes

    Science.gov (United States)

    Kesteloot, N.; Bastin, B.; Gaffney, L. P.; Wrzosek-Lipska, K.; Auranen, K.; Bauer, C.; Bender, M.; Bildstein, V.; Blazhev, A.; Bönig, S.; Bree, N.; Clément, E.; Cocolios, T. E.; Damyanova, A.; Darby, I.; De Witte, H.; Di Julio, D.; Diriken, J.; Fransen, C.; García-Ramos, J. E.; Gernhäuser, R.; Grahn, T.; Heenen, P.-H.; Hess, H.; Heyde, K.; Huyse, M.; Iwanicki, J.; Jakobsson, U.; Konki, J.; Kröll, T.; Laurent, B.; Lecesne, N.; Lutter, R.; Pakarinen, J.; Peura, P.; Piselli, E.; Próchniak, L.; Rahkila, P.; Rapisarda, E.; Reiter, P.; Scheck, M.; Seidlitz, M.; Sferrazza, M.; Siebeck, B.; Sjodin, M.; Tornqvist, H.; Traykov, E.; Van De Walle, J.; Van Duppen, P.; Vermeulen, M.; Voulot, D.; Warr, N.; Wenander, F.; Wimmer, K.; Zielińska, M.

    2015-11-01

    Coulomb-excitation experiments are performed with postaccelerated beams of neutron-deficient Po 196 ,198 ,200 ,202 isotopes at the REX-ISOLDE facility. A set of matrix elements, coupling the low-lying states in these isotopes, is extracted. In the two heaviest isotopes, Po,202200, the transitional and diagonal matrix elements of the 21+ state are determined. In Po,198196 multistep Coulomb excitation is observed, populating the 41+,02+ , and 22+ states. The experimental results are compared to the results from the measurement of mean-square charge radii in polonium isotopes, confirming the onset of deformation from 196Po onwards. Three model descriptions are used to compare to the data. Calculations with the beyond-mean-field model, the interacting boson model, and the general Bohr Hamiltonian model show partial agreement with the experimental data. Finally, calculations with a phenomenological two-level mixing model hint at the mixing of a spherical structure with a weakly deformed rotational structure.

  6. Phosphate stable oxygen isotope variability within a temperate agricultural soil.

    Science.gov (United States)

    Granger, Steven J; Harris, Paul; Peukert, Sabine; Guo, Rongrong; Tamburini, Federica; Blackwell, Martin S A; Howden, Nicholas J K; McGrath, Steve

    2017-01-01

    In this study, we conduct a spatial analysis of soil total phosphorus (TP), acid extractable phosphate (PO4) and the stable oxygen (O) isotope ratio within the PO4 molecule (δ(18)OPO4 ) from an intensively managed agricultural grassland site. Total P in the soil was found to range from 736 to 1952 mg P kg(- 1), of which between 12 and 48% was extractable using a 1 M HCl (HClPO4 ) solution with the two variables exhibiting a strong positive correlation. The δ(18)OPO4 of the extracted PO4 ranged from 17.0 to 21.6‰ with a mean of 18.8‰ (± 0.8). While the spatial variability of Total P has been researched at various scales, this is the first study to assess the variability of soil δ(18)OPO4 at a field-scale resolution. We investigate whether or not δ(18)OPO4 variability has any significant relationship with: (i) itself with respect to spatial autocorrelation effects; and (ii) HClPO4 , elevation and slope - both globally and locally. Results indicate that δ(18)OPO4 was not spatially autocorrelated; and that δ(18)OPO4 was only weakly related to HClPO4 , elevation and slope, when considering the study field as a whole. Interestingly, the latter relationships appear to vary in strength locally. In particular, the δ(18)OPO4 to HClPO4 relationship may depend on the underlying soil class and/or on different field managements that had operated across an historical north-south field division of the study field, a division that had been removed four years prior to this study.

  7. Early onset of ground state deformation in neutron-deficient polonium isotopes

    CERN Document Server

    Cocolios, T E; Andreyev, A N; Antalic, S; Barzakh, A E; Bastin, B; Buscher, J; Darby, I G; Fedorov, D V; Fedosseyev, V N; Flanagan, K T; Franchoo, S; Fritzsche, S; Huber, G; Huyse, M; Keupers, M; Koster, U; Kudryavtsev, Yu; Mane, E; Marsh, B A; Molkanov, P L; Page, R D; Sjoedin, A M; Stefan, I; Van de Walle, J; Van Duppen, P; Venhart, M; Zemlyanoy, S G; Bender, M; Heenen, P-H

    2011-01-01

    In-source resonant ionization laser spectroscopy of the even-A polonium isotopes $^{192-210,216,218}$Po has been performed using the $6p^{3} 7s^{5} S_{2}$ to $6p^{3} 7p^{5} P_{2} (\\lambda$ = 843.38 nm) transition in the polonium atom (Po-I) at the CERN ISOLDE facility. The comparison of the measured isotope shifts in $^{200-210}$Po with a previous data set allows us to test for the first time recent large-scale atomic calculations that are essential to extract the changes in the mean-square charge radius of the atomic nucleus. When going to lighter masses, a surprisingly large and early departure from sphericity is observed, which is only partly reproduced by beyond mean field calculations.

  8. Early onset of ground-state deformation in the neutron-deficient polonium isotopes

    CERN Document Server

    Cocolios, T E; Seliverstov, M D; Andreyev, A N; Antalic, S; Barzakh, A E; Bastin, B; Buscher, J; Darby, I G; Fedorov, D V; Fedosseyev, V N; Flanagan, K T; Franchoo, S; Fritzsche, S; Huber, G; Huyse, M; Keupers, M; Koster, U; Kudryavtsev, Yu; Mane, E; Marsh, B A; Molkanov, P L; Page, R D; Sjoedin, A M; Stefan, I; Van de Walle, J; Van Duppen, P; Venhart, M; Zemlyanoy, S G; Bender, M; Heenen, P H

    2011-01-01

    In-source resonant ionization laser spectroscopy of the even-$A$ polonium isotopes $^{192-210,216,218}$Po has been performed using the $6p^37s$ $^5S_2$ to $6p^37p$ $^5P_2$ ($\\lambda=843.38$ nm) transition in the polonium atom (Po-I) at the CERN ISOLDE facility. The comparison of the measured isotope shifts in $^{200-210}$Po with a previous data set allows to test for the first time recent large-scale atomic calculations that are essential to extract the changes in the mean-square charge radius of the atomic nucleus. When going to lighter masses, a surprisingly large and early departure from sphericity is observed, which is only partly reproduced by Beyond Mean Field calculations.

  9. Early Onset of Ground State Deformation in Neutron Deficient Polonium Isotopes

    Science.gov (United States)

    Cocolios, T. E.; Dexters, W.; Seliverstov, M. D.; Andreyev, A. N.; Antalic, S.; Barzakh, A. E.; Bastin, B.; Büscher, J.; Darby, I. G.; Fedorov, D. V.; Fedosseyev, V. N.; Flanagan, K. T.; Franchoo, S.; Fritzsche, S.; Huber, G.; Huyse, M.; Keupers, M.; Köster, U.; Kudryavtsev, Yu.; Mané, E.; Marsh, B. A.; Molkanov, P. L.; Page, R. D.; Sjoedin, A. M.; Stefan, I.; van de Walle, J.; van Duppen, P.; Venhart, M.; Zemlyanoy, S. G.; Bender, M.; Heenen, P.-H.

    2011-02-01

    In-source resonant ionization laser spectroscopy of the even-A polonium isotopes Po192-210,216,218 has been performed using the 6p37s S25 to 6p37p P25 (λ=843.38nm) transition in the polonium atom (Po-I) at the CERN ISOLDE facility. The comparison of the measured isotope shifts in Po200-210 with a previous data set allows us to test for the first time recent large-scale atomic calculations that are essential to extract the changes in the mean-square charge radius of the atomic nucleus. When going to lighter masses, a surprisingly large and early departure from sphericity is observed, which is only partly reproduced by beyond mean field calculations.

  10. Fine-scale spatial and interannual cadmium isotope variability in the subarctic northeast Pacific

    Science.gov (United States)

    Janssen, D. J.; Abouchami, W.; Galer, S. J. G.; Cullen, J. T.

    2017-08-01

    We present dissolved cadmium (Cd) concentrations, [Cd], and stable isotope compositions, ɛ112/110Cd, in high-resolution depth profiles from five stations along the Line P transect in the subarctic northeast Pacific Ocean. In addition to profiles collected in 2012, subsurface isopycnal samples and surface samples were collected in 2013 and 2014 respectively, providing both temporal and spatial coverage. Surface waters are characterized by Cd depletion relative to phosphate (4 3 -PO) compared to deepwater 4 3 -Cd:PO, and high inferred remineralization ratios in the nutricline (0.45nmolμmol-1) are observed, consistent with Cd enrichment relative to phosphorus (P) in surface-derived biogenic particles. The correlation between Cd and 4 3 -PO weakens at depths where oxygen is highly depleted as shown by local minima in dissolved [Cd] and the tracer Cd*. The decoupling, which is driven by a deficit of Cd relative to 4 3 -PO, appears consistent with the recent hypothesis of dissolved Cd removal in oxygen-depleted regions by insoluble metal sulfide formation. Dissolved ɛ 112 / 110Cd indicates a biologically driven fractionation in surface waters with more positive (heavy) values in the upper water column and lower (light) values in deeper waters. The highest ɛ 112 / 110Cd observed in our sample set (5.19 ± 0.23) is comparable to observations from the Southern Ocean but is significantly lighter than maximum reported surface values from the subtropical North Pacific of ɛ 112 / 110Cd ≥ 15. A global compilation of low [Cd] surface water shows similar differences in maximum ɛ 112 / 110Cd. A surface water intercalibration should be prioritized to help determine if these differences at low [Cd] reflect true physical or biological variability or are due to analytical artefacts. Surface samples from the 2012 sampling campaign fit a closed-system Rayleigh fractionation model; however, surface waters sampled in 2014 had much lower [Cd] with relatively constant ɛ 112 / 110Cd

  11. The anomalous quadrupole collectivity in Te isotopes

    CERN Document Server

    Qi, Chong

    2016-01-01

    We present systematic calculations on the spectroscopy and transition properties of even-even Te isotopes by using the large-scale configuration interaction shell model approach with a realistic interaction. These nuclei are of particular interest since their yrast spectra show a vibrational-like equally-spaced pattern but the few known E2 transitions show anomalous rotational-like behavior, which cannot be reproduced by collective models. Our calculations reproduce well the equally-spaced spectra of those isotopes as well as the constant behavior of the $B(E2)$ values in $^{114}$Te. The calculated $B(E2)$ values for neutron-deficient and heavier Te isotopes show contrasting different behaviors along the yrast line. The $B(E2)$ of light isotopes can exhibit a nearly constant bevavior upto high spins. We show that this is related to the enhanced neutron-proton correlation when approaching $N=50$.

  12. L’Art du Poète

    OpenAIRE

    Durand, Frédéric

    2013-01-01

    La poésie, c’est l’épanchement du songe dans la vie réelle. Gérard de Nerval Car Jacobsen fut un poète. Un poète dont les vers restent inégaux, laborieux et courts de souffle, mais dont bien des pages en prose méritent et appellent le culte de la prospérité. Un authentique poète, au sens où l’entendait l’auteur de Aurélia ou le Rêve de la vie, comme plus tard celui des Poèmes en prose. Toute son œuvre peut légitimement revendiquer le prestigieux bénéfice de la poésie, perpétuellement tendue q...

  13. Iron isotope composition of some Archean and Proterozoic iron formations

    Science.gov (United States)

    Planavsky, Noah; Rouxel, Olivier J.; Bekker, Andrey; Hofmann, Axel; Little, Crispin T. S.; Lyons, Timothy W.

    2012-03-01

    Fe isotopes can provide new insight into redox-dependent biogeochemical processes. Precambrian iron formations (IF) are deserving targets for Fe isotope studies because they are composed predominantly of authigenic Fe phases and record a period of unprecedented iron deposition in Earth's history. We present Fe isotope data for bulk samples from 24 Archean and Proterozoic IF and eight Phanerozoic Fe oxide-rich deposits. These data reveal that many Archean and early Paleoproterozoic iron formations were a sink for isotopically heavy Fe, in contrast to later Proterozoic and Phanerozoic Fe oxide-rich rocks. The positive δ56Fe values in IF are best explained by delivery of particulate ferric oxides formed in the water column to the sediment-water interface. Because IF are a net sink for isotopically heavy Fe, there must be a corresponding pool of isotopically light Fe in the sedimentary record. Earlier work suggested that Archean pyritic black shales were an important part of this light sink before 2.35 billion years ago (Ga). It is therefore likely that the persistently and anomalously low δ56Fe values in shales are linked with the deposition of isotopically heavy Fe in IF in the deeper parts of basins. IF deposition produced a residual isotopically light dissolved Fe pool that was captured by pyritic Fe in shales. Local dissimilatory Fe reduction in porewater and associated diagenetic reactions resulting in pyrite and carbonate precipitation may have further enhanced Fe isotope heterogeneity in marine sediments, and an 'iron shuttle' may have transported isotopically light Fe from shelf sediments to the basin. Nevertheless, water-column processing of hydrothermally delivered Fe likely had the strongest influence on the bulk iron isotope composition of Archean and Paleoproterozoic iron formations and other marine sediments.

  14. METHOD OF ISOTOPE CONCENTRATION

    Science.gov (United States)

    Spevack, J.S.

    1957-04-01

    An isotope concentration process is described which consists of exchanging, at two or more different temperature stages, two isotopes of an element between substances that are physically separate from each other and each of which is capable of containing either of the isotopes, and withdrawing from a point between at least two of the temperatare stages one of the substances containing an increased concentration of the desired isotope.

  15. Isotope products manufacture in Russia and its prospects

    Energy Technology Data Exchange (ETDEWEB)

    Malyshev, S.V.; Okhotina, I.A.; Kalelin, E.A.; Krasnov, N.N.; Kuzin, V.V.; Malykh, J.A.; Makarovsky, S.B. [Tenex, Techsnabexport Co Ltd, Moscow (Russian Federation)

    1997-10-01

    At the present stage of the world economy development, stable and radioactive isotopes,preparations and products on their base are widely used in many fields of the national economy, medicine and scientific researches. The Russian Federation is one of the largest worldwide producers of a variety of nuclide products on the base of more than 350 isotopes, as follows: stable isotopes reactor, cyclotron, fission product radioactive isotopes, ion-radiation sources compounds, labelled with stable and radioactive isotopes, radionuclide short-lived isotope generators, radiopharmaceuticals, radionuclide light and heat sources; luminous paints on base of isotopes. The Russian Ministry for Atomic Energy coordinates activity for development and organization of manufacture and isotope products supply in Russia as well as for export. Within many years of isotope industry development, there have appeared some manufacturing centres in Russia, dealing with a variety of isotope products. The report presents the production potentialities of these centres and also an outlook on isotope production development in Russia in the next years

  16. Nickel isotopic composition of the mantle

    Science.gov (United States)

    Gall, Louise; Williams, Helen M.; Halliday, Alex N.; Kerr, Andrew C.

    2017-02-01

    This paper presents a detailed high-precision study of Ni isotope variations in mantle peridotites and their minerals, komatiites as well as chondritic and iron meteorites. Ultramafic rocks display a relatively large range in δ60 Ni (permil deviation in 60 Ni /58 Ni relative to the NIST SRM 986 Ni isotope standard) for this environment, from 0.15 ± 0.07‰ to 0.36 ± 0.08‰, with olivine-rich rocks such as dunite and olivine cumulates showing lighter isotope compositions than komatiite, lherzolite and pyroxenite samples. The data for the mineral separates shed light on the origin of these variations. Olivine and orthopyroxene display light δ60 Ni whereas clinopyroxene and garnet are isotopically heavy. This indicates that peridotite whole-rock δ60 Ni may be controlled by variations in modal mineralogy, with the prediction that mantle melts will display variable δ60 Ni values due to variations in residual mantle and cumulate mineralogy. Based on fertile peridotite xenoliths and Phanerozoic komatiite samples it is concluded that the upper mantle has a relatively homogeneous Ni isotope composition, with the best estimate of δ60Nimantle being 0.23 ± 0.06‰ (2 s.d.). Given that >99% of the Ni in the silicate Earth is located in the mantle, this also defines the Ni isotope composition of the Bulk Silicate Earth (BSE). This value is nearly identical to the results obtained for a suite of chondrites and iron meteorites (mean δ60 Ni 0.26 ± 0.12‰ and 0.29 ± 0.10‰, respectively) showing that the BSE is chondritic with respect to its Ni isotope composition, with little to no Ni mass-dependent isotope fractionation resulting from core formation.

  17. PoP的发展与技术探讨

    Institute of Scientific and Technical Information of China (English)

    陆祥华

    2012-01-01

    叠层封装即PoP,主要用在信号处理和系统存储器系列中,特别在智能手机及多媒体平板电脑中的应用较广。从2005年第一代PoP产品到现在,PoP的应用呈逐年增长的势头。

  18. A new polymorph of Lu(PO33

    Directory of Open Access Journals (Sweden)

    Anis Bejaoui

    2008-08-01

    Full Text Available A new polymorph of lutetium polyphosphate, Lu(PO33, was found to be isotypic with the trigonal form of Yb(PO33. Two of the three Lu atoms occupy special positions (Wyckoff positions 3a and 3b, site symmetry overline{3}. The atomic arrangement consists of infinite helical polyphosphate chains running along the c axis, with a repeat period of 12 PO4 tetrahedra, joined with LuO6 octahedra.

  19. A global Ge isotope budget

    Science.gov (United States)

    Baronas, J. Jotautas; Hammond, Douglas E.; McManus, James; Wheat, C. Geoffrey; Siebert, Christopher

    2017-04-01

    We present measurements of Ge isotope composition and ancillary data for samples of river water, low- and high-temperature hydrothermal fluids, and seawater. The dissolved δ74Ge composition of analyzed rivers ranges from 2.0 to 5.6‰, which is significantly heavier than previously determined values for silicate rocks (δ74Ge = 0.4-0.7‰, Escoube et al., Geostand. Geoanal. Res., 36(2), 2012) from which dissolved Ge is primarily derived. An observed negative correlation between riverine Ge/Si and δ74Ge signatures suggests that the primary δ74Ge fractionation mechanism during rock weathering is the preferential incorporation of light isotopes into secondary weathering products. High temperature (>150 °C) hydrothermal fluids analyzed in this study have δ74Ge of 0.7-1.6‰, most likely fractionated during fluid equilibration with quartz in the reaction zone. Low temperature (25-63 °C) hydrothermal fluids are heavier (δ74Ge between 2.9‰ and 4.1‰) and most likely fractionated during Ge precipitation with hydrothermal clays. Seawater from the open ocean has a δ74Gesw value of 3.2 ± 0.4‰, and is indistinguishable among the different ocean basins at the current level of precision. This value should be regulated over time by the isotopic balance of Ge sources and sinks, and a new compilation of these fluxes is presented, along with their estimated isotopic compositions. Assuming steady-state, non-opal Ge sequestration during sediment authigenesis likely involves isotopic fractionation Δ74Gesolid-solution that is -0.6 ± 1.8‰.

  20. Statistical clumped isotope signatures

    NARCIS (Netherlands)

    Röckmann, T.; Popa, M. E.; Krol, M. C.; Hofmann, M. E. G.

    2016-01-01

    High precision measurements of molecules containing more than one heavy isotope may provide novel constraints on element cycles in nature. These so-called clumped isotope signatures are reported relative to the random (stochastic) distribution of heavy isotopes over all available isotopocules of a m

  1. Optimization of partially shaded PV array using a modified P&O MPPT algorithm

    Directory of Open Access Journals (Sweden)

    Abdelaziz YOUCEF

    2016-07-01

    Full Text Available A photovoltaic (PV array generated power is directly affected by temperature, solar irradiation, shading, and array configuration. In practice, PV arrays could be partially shaded by could, buildings, trees and other utilities. In this case, multiple maximums appear in the P-V curve, a global maximum and one or several local maximums. The “perturb and observe“ (P&O maximum power point tracking (MPPT algorithm cannot differentiate between a global and a local maximum and it is therefore ineffective when partial shading occurs. First, this paper presents an original mathematical model of the P-V curve of a partially shaded PV array, that was used to perform a simulation study in order to show the P&O algorithm inability to track the global MPP of a PV array solar system under partial shading for low shading irradiation levels, then an adaptation sub algorithm is proposed to be added to the P&O algorithm in order to give it the ability to track the global MPP. This sub algorithm moves the operating point imposed by the partial shading configuration to a point in the vicinity of the global MPP in order to be easily tracked by the P&O algorithm. In the simulation, a PV array with a hundred modules has been considered by using a light, a medium then a severe shading configuration. The results obtained indicate that the proposed modified P&O algorithm is able to track the global MPP for the considered shading configurations and for any shading irradiation level.

  2. Degradation Studies on LiFePO4 cathode

    DEFF Research Database (Denmark)

    Scipioni, Roberto; Jørgensen, Peter Stanley; Hjelm, Johan

    2015-01-01

    In this paper we examine a laboratory LiFePO4 (LFP) cathode and propose a simple model that predicts the electrode capacity as function of C-rate, number of cycles and calendar time. Microcracks were found in Li1-xFePO4 particles in a degraded LFP electrode and low-acceleration voltage (1 kV) FIB....../SEM analysis allowed us to obtain phase contrast between FePO4 and LiFePO4. The evolution of micro-cracks is expected to increase the concentration of LFP particles which are not electronically accessible and thus cause a loss in capacity....

  3. Sodium samarium tetrakis(polyphosphate, NaSm(PO34

    Directory of Open Access Journals (Sweden)

    Dan Zhao

    2010-07-01

    Full Text Available NaSm(PO34 has been prepared by solid state reactions. It belongs to type II of the structural family of MILnIII(PO34 compounds (MI = alkali metal and LnIII = rare earth metal and is composed of ∞(PO3n]n− polyphosphate chains with a repeating unit of four PO4 tetrahedra. The chains extend parallel to [100] and share O atoms with irregular SmO8 polyhedra, forming a three-dimensional framework which delimits tunnels occupied by Na+ cations in a distorted octahedral environment.

  4. Ce and Eu activated Na2Zn5(PO4)4, a new promising novel phosphor

    Indian Academy of Sciences (India)

    K N Shinde; S J Dhoble; Animesh Kumar

    2011-07-01

    A new efficient phosphor, Eu2+/Eu3+ and Ce3+ activated Na2Zn5(PO4)4 has been synthesized by solid-state reaction technique at high temperature. X-ray powder diffraction analysis confirmed the formation of Na2Zn5(PO4)4 host lattice. Scanning electron microscopy indicated that the microstructure of the phosphor consisted of irregular fine grains with a size of about 0.5–2 m. Photoluminescence excitation spectrum measurements of Ce3+ activated Na2Zn5(PO4)4 show that the phosphor can be efficiently excited by UV-Vis light from 280 to 310 nm to realize emission in the visible (blue) range due to the 5–4 transition of Ce3+ ions which is applicable for scintillation purpose, whereas Eu2+/Eu3+ activated Na2Zn5(PO4)4 phosphor emits blue, green and red emission spectrum shows at 487 nm, 546 nm with a dominant peak at 611 nm respectively, due to Eu2+/Eu3+ ions which is promising candidate for solid state lighting. Therefore, newly synthesised, by low cost and easy technique prepared, novel phosphors may be useful as RGB phosphor for solid state lighting application.

  5. Comparative studies on Ag{sub 3}PO{sub 4}/BiPO{sub 4}–metal-organic framework–graphene-based nanocomposites for photocatalysis application

    Energy Technology Data Exchange (ETDEWEB)

    Mohaghegh, N. [Department of Chemistry, Sharif University of Technology, Azadi Avenue, Tehran (Iran, Islamic Republic of); Tasviri, M., E-mail: m_tasviri@sbu.ac.ir [Department of Chemistry, Shahid Beheshti University, Evin, P.O. Box 19839-63113, Tehran (Iran, Islamic Republic of); Rahimi, E. [Department of Mining Engineering, Islamic Azad University, South Tehran Branch, Tehran (Iran, Islamic Republic of); Gholami, M.R., E-mail: gholami@sharif.edu [Department of Chemistry, Sharif University of Technology, Azadi Avenue, Tehran (Iran, Islamic Republic of)

    2015-10-01

    Graphical abstract: - Highlights: • Novel Ag{sub 3}PO{sub 4}/BiPO{sub 4} (AB)–graphene-based photocatalysts were reported. • Photocatalytic degradation mechanism of Atrazine herbicide was investigated. • It was divulged that the photodegradation is increased by AB supporting. • Enhanced photodegradation has been obtained by the AB/Cu(tpa).GR nanocomposite. • The unique heterojunction formed by coupling Cu(tpa) with GR caused high activity. - Abstract: For the first time, we report novel Ag{sub 3}PO{sub 4}/BiPO{sub 4} (AB)–graphene-based photocatalysts. The fabricated nanocomposites were characterized by various techniques. The photocatalytic properties of the prepared catalysts were evaluated by the photodegradation of Atrazine herbicide under both visible and UV light irradiation. Atrazine concentration was determined using the spectrophotometric method according to the Konig's reaction by monitoring the absorbance at 470 nm wavelength during the photodegradation process. Both degradation rate and efficiency using graphene (GR)-based nanocomposites are found to be much better than using pure AB. Atrazine photodegradation displayed that the AB supporting is an important point to become a great photocatalyst for this reaction. Enhanced photodegradation has been obtained by the AB/Cu(tpa).GR nanocomposite. The results showed that the novel synthesized AB/Cu(tpa).GR nanocomposite exhibits a dramatic separation of photogenerated electron/hole pairs. This was accounted for by the improved efficiency of an interfacial charge separation, thanks to the unique heterojunction formed by coupling Cu(tpa) with GR. Chemical oxygen demand of herbicide solution was measured and it posed a good idea about Atrazine herbicide degradation.

  6. Facile deposition of Ag{sub 3}PO{sub 4} on graphene-like MoS{sub 2} nanosheets for highly efficient photocatalysis

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Peifu [College of Environmental and Chemical Engineering, Shanghai University of Electric Power, Shanghai 200090 (China); Shi, Penghui, E-mail: shipenghui@shiep.edu.cn [College of Environmental and Chemical Engineering, Shanghai University of Electric Power, Shanghai 200090 (China); Hong, Yuanchen; Zhou, Xuejun [College of Environmental and Chemical Engineering, Shanghai University of Electric Power, Shanghai 200090 (China); Yao, Weifeng, E-mail: yaoweifeng@shiep.edu.cn [College of Environmental and Chemical Engineering, Shanghai University of Electric Power, Shanghai 200090 (China); Shanghai Key Laboratory of Materials Protection and Advanced Materials in Electric Power, Shanghai University of Electric Power, Shanghai 200090 (China)

    2015-02-15

    Graphical abstract: The photocatalytic performance of Ag{sub 3}PO{sub 4} was highly improved by the in situ deposition of Ag{sub 3}PO{sub 4} particles on graphene-like MoS{sub 2} nanosheets. - Highlights: • A novel composite photocatalyst was synthesized by depositing Ag{sub 3}PO{sub 4} on the graphene-like MoS{sub 2} nanosheets. • Ag{sub 3}PO{sub 4}/MoS{sub 2} photocatalyst exhibited a high photocatalytic activity for RhB degradation. • Graphene-like MoS{sub 2} nanosheets. • MoS{sub 2} nanosheets play an important role in photocatalytic activity by serving as an effective acceptor of the photogenerated carriers. - Abstract: A facile method for the in situ deposition of Ag{sub 3}PO{sub 4} on graphene-like MoS{sub 2} nanosheets was developed to improve the photocatalytic performance of Ag{sub 3}PO{sub 4} catalysts. The heterostructure of Ag{sub 3}PO{sub 4}/MoS{sub 2} composites was characterized by using X-ray diffraction spectra (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). The prepared Ag{sub 3}PO{sub 4}/MoS{sub 2} photocatalyst exhibited a much higher photocatalytic activity than that of Ag{sub 3}PO{sub 4} for the degradation of Rhodamine B (RhB) under visible light irradiation (>400 nm). The improved photocatalytic activity of Ag{sub 3}PO{sub 4}/MoS{sub 2} is attributed to the efficient separation of photogenerated electron–hole pairs in the composite. This result provides a new perspective on the design of high-performance photocatalysts which is promising for energy applications.

  7. Effect of Ag+ and PO43- ratios on the microstructure and photocatalytic activity of Ag3PO4

    Science.gov (United States)

    Qin, Jiaqian; Zhang, Xinyu; Yang, Chengwu; Song, Aijun; Zhang, Bing; Rajendran, Saravanan; Ma, Mingzhen; Liu, Riping

    2016-09-01

    In this work, the catalyst silver phosphate (Ag3PO4) with different initial ratios of Ag+ and PO43- in aqueous solution was synthesized by a simple precipitation method from AgNO3 and NH4H2PO4 which were used as the precursor. After that, the prepared samples were characterized by different techniques such as field emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD), UV-visible diffuse reflectance spectroscopy (UV-DRS) and decomposition evolution of rhodamine B (RhB) solution. The results indicate that the initial ratios of Ag+/PO43- in aqueous solution can modify the morphology and also it can significantly affect the photocatalytic performance. During photocatalytic process, the rich Ag+ ion Ag3PO4 can form the surface plasmon resonance (SPR) of Ag nanoparticles, which inhibit the reduction of Ag3PO4 resulting in higher photocatalytic activity and stability.

  8. Luminescence properties of red phosphors Ca10Li (PO4)7:Eu3+

    Institute of Scientific and Technical Information of China (English)

    SONG Enhai; ZHAO Weiren; ZHOU Guoxiong; DOU Xihua; YI Chunyu; ZHOU Minkang

    2011-01-01

    A series of red phosphors Ca10Li (PO4)7:Eu3+ were synthesized by high temperature solid-state reaction method. Their luminescence properties were characterized by means of photoluminescence excitation and emission spectra, CIE chromaticity and quantum efficiency. Results indicated that the phosphors could be effectively excited by the near ultraviolet (NUV) light (393 nm). The main emission peaks of the phosphor were ascribed to the transition 5D0-7F2 (613 and 617 nm) of Eu3+ ion when samples were excited by 393 nm. The CIE chromaticity (x,y) of Ca9.9Li (PO4)7:0.10Eu3+ was x=0.638, y=0.361 and the quantum efficiency of this phosphor was 75% excited by 393 nm.Therefore, this phosphor could be a promising red component for the applications in white LEDs.

  9. Neutron-rich polonium isotopes studied with in-source laser spectroscopy

    CERN Document Server

    Dexters, Wim; Cocolios, T E

    This work studies the unknown region of neutron rich polonium isotopes. The polonium isotopes, with Z=84, lie above the magic lead nuclei (Z=82). The motivation for this research can mainly be found in these lead nuclei. When looking at the changes in the mean square charge radii beyond the N=126 shell gap, a kink is observed. This kink is also found in the radon (Z=86) and radium (Z=88) isotopes. The observed effect cannot be reproduced with our current models. The polonium isotopes yield more information on the kink and they are also able to link the known charge radii in lead isotopes to those in radon and radium. Additionally, the nuclear moments of the odd-neutron isotope $^{211}$Po are investigated. This nucleus has two protons and one neutron more than the doubly magic nucleus $^{208}$Pb. Nuclear moments of isotopes close to this doubly magic nucleus are good tests for the theoretic models. Besides pushing the models to their limits, the nuclear moments of $^{211}$Po also yield new information on the f...

  10. Generation of Radixenon Isotopes

    Energy Technology Data Exchange (ETDEWEB)

    McIntyre, Justin I.; Bowyer, Ted W.; Hayes, James C.; Heimbigner, Tom R.; Morris, Scott J.; Panisko, Mark E.; Pitts, W. K.; Pratt, Sharon L.; Reeder, Paul L.; Thomas, Charles W.

    2003-06-30

    Pacific Northwest National Laboratory has developed an automated system for separating Xe from air and can detect the following radioxenon isotopes, 131mXe, 133mXe, 133Xe, and 135Xe. This report details the techniques used to generate the various radioxenon isotopes that are used for the calibration of the detector as well as other isotopes that have the potential to interfere with the fission produced radioxenon isotopes. Fission production is covered first using highly enriched uranium followed by a description and results from an experiment to produce radioxenon isotopes from neutron activation of ambient xenon.

  11. Isotopes in heterogeneous catalysis

    CERN Document Server

    Hargreaves, Justin SJ

    2006-01-01

    The purpose of this book is to review the current, state-of-the-art application of isotopic methods to the field of heterogeneous catalysis. Isotopic studies are arguably the ultimate technique in in situ methods for heterogeneous catalysis. In this review volume, chapters have been contributed by experts in the field and the coverage includes both the application of specific isotopes - Deuterium, Tritium, Carbon-14, Sulfur-35 and Oxygen-18 - as well as isotopic techniques - determination of surface mobility, steady state transient isotope kinetic analysis, and positron emission profiling.

  12. On Left π-regular po-semigroups%关于左π-正则po-半群

    Institute of Scientific and Technical Information of China (English)

    许新斋

    2001-01-01

    本文在po-半群和半群中引进了一致π-半素族的概念,并给出了左π-正则po-半群的若干刻划.这些刻划推广了N.Kehayopulu在文[1]中给出的一些结果.%In this paper, the concept of uniform π-semiprime family in po-semigroups and semigroups is introduced. We give characterizations of left π-regular po-semigroups which generalize the results given by N. Kehayopulu in [1].

  13. PoE交换机设计与配置管理%Design and Configuration of PoE Switch

    Institute of Scientific and Technical Information of China (English)

    刘嘉滨

    2012-01-01

    在WLAN业务和安防网络视频监控业务中需部署大量无线AP和IP Camera设备,为解决部署在特殊位置上设备取电问题,可通过PoE技术进行远程供电.结合成熟的网络交换机技术,PoE交换机随之出现.通过介绍PoE交换机设计与配置,进一步加深对PoE技术的认识.这种设计和配置的PoE交换机已在市场上成功应用.%Lots of wireless AP and IP camera devices have to be deployed in WLAN and monitors. In order to provide power supply for devices in special positions, the Power over Ethernet technology can be utilized. In combination with the ripe switch technology, PoE switches appear. By introducing the design and configuration of the PoE switch, the PoE technology can be further understood. And this type of PoE switch has appeared in the market.

  14. Ergonomia nos dispositivos poéticos

    OpenAIRE

    Vasconcelos, Edmilson

    2004-01-01

    Dissertação (mestrado) - Universidade Federal de Santa Catarina, Centro Tecnológico. Programa de Pós-Graduação em Engenharia de Produção. O presente estudo busca na Ergonomia a solução para uma problemática constatada na relação entre o espectador e as obras de arte participo-interativas da arte contemporânea - os dispositivos poéticos. Esta problemática vai, desde a destruição das obras através de participações conflituosas, até a inadequações institucionais de agentes oficiais do Sistema...

  15. Stable Chlorine Isotope Study: Application to Early Solar System Materials

    Science.gov (United States)

    Mala,ira. M/; Nyquist, L. E.; Reese, Y.; Shih, C-Y; Fujitani, T.; Okano, O.

    2010-01-01

    A significantly large mass fractionation between two stable chlorine isotopes is expected during planetary processes In addition, in view of the isotopic heterogeneity of other light elements, the chlorine isotopes can potentially be used as a tracer for the origins and evolutionary processes of early solar system materials. Due to analytical difficulties, however, current chlorine isotope studies on planetary materials are quite controversial among IRMS (gas source mass spectrometry) and/or TIMS (Thermal Ionization Mass Spectrometry) groups [i.e. 1-3]. Although a cross-calibration of IRMS and TIMS indicates that both techniques are sufficiently consistent with each other [4], some authors have claimed that the Cl-37/Cl-35 ratio of geological samples obtained by TIMS technique are, in general, misleadingly too high and variable compared to those of IRMS [3]. For example, almost no differences of Cl isotope composition were observed among mantle materials and carbonaceous meteorites by [3]. On the other hand, according to more recent IRMS work [2], significant Cl isotope variations are confirmed for mantle materials. Therefore, additional careful investigation of Cl isotope analyses are now required to confirm real chlorine isotope variations for planetary materials including carbonaceous chondrites [5]. A significantly large mass fractionation between two stable chlorine isotopes is expected during planetary processes In addition, in view of the isotopic heterogeneity of other light elements, the chlorine isotopes can potentially be used as a tracer for the origins and evolutionary processes of early solar system materials. Due to analytical difficulties, however, current chlorine isotope studies on planetary materials are quite controversial among IRMS (gas source mass spectrometry) and/or TIMS (Thermal Ionization Mass Spectrometry) groups [i.e. 1-3]. Although a cross-calibration of IRMS and TIMS indicates that both techniques are sufficiently consistent with each

  16. REVIEW: TALES OF KHA BA DKAR PO

    Directory of Open Access Journals (Sweden)

    Jundan (Jasmine Zhang

    2015-03-01

    Full Text Available Review of: Jing Guo . 2012. Xue shan zhi shu [Tales of Kha ba dkar po] [ཁ་བ་དཀར་པོ]. Kunming: Yunnan People's Press. My favorite color is to add a little white on the whiteness, as if there was a snow-white eagle landing on a snow-covered mountain rock. My favorite color is to add a bit green on the greenness, as if there was an emerald parrot flying in the wild walnut woods. Deqin xianzi lyrics. These lyrics evoke a space beyond a sense of realism. In his book, Tales of Kha ba dkar po (ToK, Guo mentions these lines three times, suggesting a transcendental experience one may encounter in Tibetan areas while, at the same time, humbled by the mindset of human nature relations enacted by Tibetan people. ToK is, in many ways, a valuable academic work. Guo's favorite lines of xianzi allude to a 'space-in-between' the secular and sacred, which provides a unique experience for a broad readership, and induces the readers to deeper reflections on topics such as 'nature/ culture', 'belief', 'rite', and 'life/ death'. ToK is one of nineteen contemporary anthropological and ethnological works conducted in Yunnan Province, Southwest China and published in the 'Anthropology and Ethnology series in Contemporary China'. In the preface for the series, Yin (2012 suggests that there are two primary reasons for the somewhat slow development of Chinese scholarship in the field of anthropology and ethnology. One is the historically Han-centered intellectual atmosphere, and the other is the ideological ambivalence that ethnic culture has faced since the establishment of the People's Republic of China. In this context, Guo's longitudinal academic and intellectual engagement with the Tibetan communities in northwest Yunnan is included in this series as part of the increasing recognition of the significance of understanding southwest China's complex ethnic and cultural diversity.

  17. Isotope determination of sulfur by mass spectrometry in soil samples

    Directory of Open Access Journals (Sweden)

    Alexssandra Luiza Rodrigues Molina Rossete

    2012-12-01

    Full Text Available Sulphur plays an essential role in plants and is one of the main nutrients in several metabolic processes. It has four stable isotopes (32S, 33S, 34S, and 36S with a natural abundance of 95.00, 0.76, 4.22, and 0.014 in atom %, respectively. A method for isotopic determination of S by isotope-ratio mass spectrometry (IRMS in soil samples is proposed. The procedure involves the oxidation of organic S to sulphate (S-SO4(2-, which was determined by dry combustion with alkaline oxidizing agents. The total S-SO4(2- concentration was determined by turbidimetry and the results showed that the conversion process was adequate. To produce gaseous SO2 gas, BaSO4 was thermally decomposed in a vacuum system at 900 ºC in the presence of NaPO3. The isotope determination of S (atom % 34S atoms was carried out by isotope ratio mass spectrometry (IRMS. In this work, the labeled material (K2(34SO4 was used to validate the method of isotopic determination of S; the results were precise and accurate, showing the viability of the proposed method.

  18. Co(II)–grafted Ag{sub 3}PO{sub 4} photocatalysts with unexpected photocatalytic ability: Enhanced photogenerated charge separation efficiency, photocatalytic mechanism and activity

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Shuna [College of Textile Engineering, Zhejiang Industry Polytechnic College, Shaoxing 312000 (China); Zhang, Shujuan, E-mail: zhangshujuan@tust.edu.cn [College of Science, Tianjin University of Science & Technology, Tianjin 300457 (China); 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)

    2015-08-15

    Highlights: • Co–Ag{sub 3}PO{sub 4} with higher photodegradation ability was synthesized. • ·OH was the main active species in the oxidation of MO. • The synergy of Co(II) and Ag{sub 3}PO{sub 4} greatly enhanced the separation efficiency. - Abstract: Since the photocatalytic capability is determined by the separation and transmission efficiency of photoinduced charges, its improvement remains a challenge for development of efficient photocatalysts. Here, we made large improvement on the surface of Ag{sub 3}PO{sub 4} using Co(II)–grafted Ag{sub 3}PO{sub 4} by a hydrothermal method. During the photocatalytic process, Co(II) was oxidized to Co(III) by the photogenerated holes under visible light radiation, which enhanced the separation efficiency of photogenerated charges. Meanwhile, the Co(III) as-formed could oxidize dye molecules, which recovered the Co(II). The synergy of Co(II) and Ag{sub 3}PO{sub 4} greatly promoted the separation and transmission efficiency of the photogenerated charges, and severely improved the photocatalytic activity of Ag{sub 3}PO{sub 4}. The surface grafted Co(II) on Ag{sub 3}PO{sub 4} is responsible for the enhancement of photocatalytic activity.

  19. Separation and electrodeposited of {sup 210} Po; Separacion y electrodeposito de {sup 210} Po

    Energy Technology Data Exchange (ETDEWEB)

    Ordonez R, E.; Iturbe G, J.L

    1991-12-15

    Presently work it was determined the selective separation of the {sup 210} Po that is in an uraniferous mineral, by means of acid leaching of the mineral and the purification was carried out by means of partition chromatography whose stationary phase is 2-ethylhexyl phosphoric acid (D{sub 2}EHPA), it has been possible to isolate the {sup 210} Po of the rest of the radioactive elements that conform the family 4 N{sup +2}, the optimal elutriation conditions of this element were settled down of manner of not dragging other radioelements. Another of the achievements presented in this communication has been the electrodeposition of this element has more than enough stainless steel discs with a superior yield to 95%. (Author)

  20. Isotopic Fractionation of Selenium Oxyanions in Wetlands

    Science.gov (United States)

    Clark, S. K.; Johnson, T. M.

    2004-05-01

    species-specific information than those from previous studies, but they similarly suggest that Se(VI) uptake is dominated by plant or algae assimilation: a process that involves little or no isotopic fractionation. On the other hand, Se(IV) is likely reduced by microbes or abiotic reductants in the sediments. The slight shift toward isotopically lighter Se(VI) is enigmatic, but could be due to oxidation of isotopically light dimethylselenide to Se(VI) in the water column.

  1. Isotopic Evidence of Unaccounted for Fe and Cu Erythropoietic Pathways

    Science.gov (United States)

    Albarede, F.; Telouk, P.; Lamboux, A.; Jaouen, K.; Balter, V.

    2011-12-01

    Despite its potential importance for understanding perturbations in the Fe-Cu homeostatic pathways, the natural isotopic variability of these metals in the human body remains unexplored. We measured the Fe, Cu, and Zn isotope compositions of total blood, serum, and red blood cells of ~50 young blood donors by multiple-collector ICP-MS after separation and purification by anion exchange chromatography. Zn is on average 0.2 permil heavier in erythrocytes (δ 66Zn=0.44±0.33 permil) with respect to serum but shows much less overall isotopic variability than Fe and Cu, which indicates that isotope fractionation depends more on redox conditions than on ligand coordination. On average, Fe in erythrocytes (δ 56Fe=-2.59±0.47 permil) is isotopically light by 1-2 permil with respect to serum, whereas Cu in erythrocytes (δ 65Cu=0.56±0.50 permil) is 0.8 percent heavier. Fe and Cu isotope compositions clearly separate erythrocytes of men and women. Fe and Cu from B-type men erythrocytes are visibly more fractionated than all the other blood types. Isotope compositions provide an original method for evaluating metal mass balance and homeostasis. Natural isotope variability shows that the current models of Fe and Cu erythropoiesis, which assume that erythropoiesis is restricted to bone marrow, violate mass balance requirements. It unveils unsuspected major pathways for Fe, with erythropoietic production of isotopically heavy ferritin and hemosiderin, and for Cu, with isotopically light Cu being largely channeled into blood and lymphatic circulation rather than into superoxide dismutase-laden erythrocytes. Iron isotopes provide an intrinsic measuring rod of the erythropoietic yield, while Cu isotopes seem to gauge the relative activity of erythropoiesis and lymphatics.

  2. Isotopic discrimination of zinc in higher plants.

    Science.gov (United States)

    Weiss, D J; Mason, T F D; Zhao, F J; Kirk, G J D; Coles, B J; Horstwood, M S A

    2005-03-01

    * The extent of isotopic discrimination of transition metals in biological processes is poorly understood but potentially has important applications in plant and biogeochemical studies. * Using multicollector inductively coupled plasma (ICP) mass spectrometry, we measured isotopic fractionation of zinc (Zn) during uptake from nutrient solutions by rice (Oryza sativa), lettuce (Lactuca sativa) and tomato (Lycopersicon esculentum) plants. * For all three species, the roots showed a similar extent of heavy Zn enrichment relative to the nutrient solution, probably reflecting preferential adsorption on external root surfaces. By contrast, a plant-species specific enrichment of the light Zn isotope occurred in the shoots, indicative of a biological, membrane-transport controlled uptake into plant cells. The extent of the fractionation in the shoots further depended on the Zn speciation in the nutrient solution. * The observed isotopic depletion in heavy Zn from root to shoot (-0.13 to -0.26 per atomic mass unit) is equivalent to roughly a quarter of the total reported terrestrial variability of Zn isotopic compositions (c. 0.84 per atomic mass unit). Plant uptake therefore represents an important source of isotopic variation in biogeochemical cycling of Zn.

  3. Iron isotopic fractionation during continental weathering

    Energy Technology Data Exchange (ETDEWEB)

    Fantle, Matthew S.; DePaolo, Donald J.

    2003-10-01

    The biological activity on continents and the oxygen content of the atmosphere determine the chemical pathways through which Fe is processed at the Earth's surface. Experiments have shown that the relevant chemical pathways fractionate Fe isotopes. Measurements of soils, streams, and deep-sea clay indicate that the {sup 56}Fe/{sup 54}Fe ratio ({delta}{sup 56}Fe relative to igneous rocks) varies from +1{per_thousand} for weathering residues like soils and clays, to -3{per_thousand} for dissolved Fe in streams. These measurements confirm that weathering processes produce substantial fractionation of Fe isotopes in the modern oxidizing Earth surface environment. The results imply that biologically-mediated processes, which preferentially mobilize light Fe isotopes, are critical to Fe chemistry in weathering environments, and that the {delta}{sup 56}Fe of marine dissolved Fe should be variable and negative. Diagenetic reduction of Fe in marine sediments may also be a significant component of the global Fe isotope cycle. Iron isotopes provide a tracer for the influence of biological activity and oxygen in weathering processes through Earth history. Iron isotopic fractionation during weathering may have been smaller or absent in an oxygen-poor environment such as that of the early Precambrian Earth.

  4. Preparation of Partial Spherical LiFePO4 Using Spherical Li3PO4 as Aprecursor%以球形Li3PO4制备球形LiFePO4

    Institute of Scientific and Technical Information of China (English)

    于春洋; 潘志红

    2007-01-01

    以曲拉通100作表面活性剂,用超声波法制备了球形度较好、平均粒径为10μm的球形Li3PO4.以球形Li3PO4为前驱体制备了部分球形的LiFePO4,并对其电化学性能进行了研究.由该法制备的LiFePO4振实密度为1.20 g/cm3,较其他方法制备的LiFePO4密度有所提高.

  5. Anisotropic lithium ion migration in LiFePO4

    Science.gov (United States)

    Park, S. B.; Park, C. K.; Hwang, J. T.; Cho, W. I.; Jang, H.

    2011-12-01

    An anisotropic behavior of lithium ion migration in LiFePO4 is investigated using the cathode particles after chemical delithiation. A phase contrast of a LiFePO4 particle validating the directional property is also found. It suggests that the lithium ion migration path is limited to the [010] direction and the phase boundary between LiFePO4 and FePO4 is perpendicular [010]. The symmetric phase boundary inside the LiFePO4 particle is contrary to the non-directional core-shell model reported by others. The molecular dynamics simulation confirms the crystallographic direction with the lowest energy for lithium ion migration.

  6. The behaviour of copper isotopes during igneous processes

    Science.gov (United States)

    Savage, P. S.; Moynier, F.; Harvey, J.; Burton, K. W.

    2015-12-01

    Application of Cu isotopes to high temperature systems has recently gained momentum and has the potential for probing sulphide fractionation during planetary differentiation [1]. This requires robust estimates for planetary reservoirs, and a fundamental understanding of how igneous processes affect Cu isotopes; this study aims to tackle the latter. Cogenetic suites affected by both fractionation crystallisation and cumulate formation were analysed to study such effects on Cu isotopes. In S-undersatured systems, Cu behaves incompatibly during melt evolution and the Cu isotope composition of such melt is invariant over the differentiation sequence. In contrast, S-saturated systems show resolvable Cu isotope variations relative to primitive melt. Such variations are minor but imply a slightly heavy Cu isotope composition for continental crust compared to BSE, consistent with granite data [2]. Although olivine accumulation does not affect Cu isotopes, spinel-hosted Cu is isotopically light relative to the bulk. Analysis of variably melt-depleted cratonic peridotites shows that partial melting can affect Cu isotope composition in restite, with the depleted samples isotopically light compared to BSE. This could be due to residual spinel and/or incongruent melting of sulphides - individual sulphides picked from a single xenolith reveal a range of Cu isotope compositions, dependent on composition. Although partial melting may fractionate Cu isotopes, models suggest most mantle-derived melt will have δ65Cu ≈ BSE, as most source Cu will be transferred to the melt. Small degree melts such as ocean island basalts are predicted to be isotopically heavier than MORB, if derived from a primitive mantle source. OIBs have a range of Cu isotope compositions: some are heavier than MORB as predicted; however, some have much lighter compositions. Since Cu isotopes can be significantly fractionated in the surface environment [e.g. 3] OIB Cu isotopic variations may be linked to

  7. Synthesis and luminescence properties of Eu2+-activated Ca4Mg5(PO4)6 for blue-emitting phosphor

    Indian Academy of Sciences (India)

    Liu Min; Tang Wanjun; Deng Kejian

    2012-02-01

    Ca4Mg5(PO4)6:Eu2+ blue-emitting phosphor was synthesized by the combustion-assisted synthesis method under reductive atmosphere. The products were characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM) and photoluminescence (PL) spectrum. XRD analysis confirmed the formation of Ca4Mg5(PO4)6 pure phase. Photoluminescence results showed that the phosphor can be excited efficiently by UV light range from 230–400 nm, and then exhibited bright blue light with peak wavelength at 431 nm. It is a very promising candidate as a blue-emitting phosphor for potential applications in display devices.

  8. Mechanical and thermal-expansion characteristics of Ca10(PO46(OH2-Ca3(PO42 composites

    Directory of Open Access Journals (Sweden)

    Ruseska G.

    2006-01-01

    Full Text Available Three types of composites consisting of Ca10(PO46(OH2 and Ca3(PO42 with composition: 75% (wt Ca10(PO46(OH2: 25%(wt Ca3(PO42; 50%(wt Ca10(PO46(OH2: 50%(wtCa3(PO42 and 25 %(wt Ca10(PO46(OH2: 75%(wt Ca3(PO42 were the subject of our investigation. Sintered compacts were in thermal equilibrium, which was proved by the absence of hysteresis effect of the dependence ΔL/L=f(T during heating /cooling in the temperature interval 20-1000-200C. Sintered compacts with the previously mentioned composition possess 26-50% higher values of the E-modulus, G-modulus and K-modulus indicating the presence of a synergism effect. Several proposed model equations for predicting the thermal expansion coefficient in dependence of the thermal and elastic properties of the constitutive phases and their volume fractions, given by: Turner, Kerner, Tummala and Friedberg, Thomas and Taya, were used for making correlations between mechanical and thermal-expansion characteristics of the Ca10(PO46(OH2 - Ca3(PO42 composites. Application of the previously mentioned model equations to all kinds of composites leads to the conclusion that the experimentally obtained results for the thermal expansion coefficient are in an excellent agreement with the theoretical calculated values on account of the volume fraction of each constitutive phase and with all applied model equations, with a coefficient of correlation from 98.16-99.86 %.

  9. Combustion synthesis and luminescence properties of blue NaBaPO4:Eu2+ phosphor

    Institute of Scientific and Technical Information of China (English)

    SUN Jiayue; ZHANG Xiangyan; DU Haiyan

    2012-01-01

    The blue-emitting phosphor NaBaPO4:Eu2+ was prepared by the combustion method.The phase structure and microstructure of the as-prepared samples were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM),respectively.Under the excitation wavelength of 360 nm,the emission spectrum exhibited only one blue band centering at 435 nm,which was ascribed to the 4f65d1→4f7transition on Eu2+ ions.Compared with the phosphor obtained by solid-state reaction method,the relative emission intensity of sample obtained by combustion method increased slightly.The decay times and the temperature dependence luminescence intensities (25-300 ℃) were discussed in order to further investigate the potential applications.Furthermore,Eu2+-doped NaBaPO4 phosphor showed higher thermally stable luminescence comparable to commercially available Y3Al5O12:Ce3+ (Y AG:Ce3+) phosphor.All the investigated suggestions that Na-BaPO4:Eu2+ is a good phosphor candidate applied in white light emitting diode.

  10. Synthesis and characterization of Mn2+ doped CdOZn3(PO4)2 nanocomposites

    Science.gov (United States)

    Naga Bhaskararao, Y.; Satyavathi, K.; Subba Rao, M.; Cole, Sandhya

    2017-02-01

    Undoped and Mn2+ doped CdOZn3(PO4)2 nanocomposites are fruitfully synthesized by chemical precipitation process at room temperature. The morphology, structure and spectroscopic properties of the prepared samples are characterized by X-ray diffraction (XRD), optical absorption, Scanning electron microscope (SEM) with EDS, Fourier transform infrared (FT-IR) spectroscopy, Photolumiscence (PL) and Electron Paramagnetic Resonance (EPR). XRD data confirms the cubic phase of CdO and monoclinic phase of Zn3(PO4)2. Strain and dislocation density are also calculated from XRD studies. Optical absorption spectrum of Mn2+ doped CdOZn3(PO4)2 nanocomposite shows different spin-forbidden DMSO-d6 bands which are the characteristics of octahedral site symmetry related to Mn2+. The crystal field parameter Dq and inter electronic repulsion parameters (B and C) are deliberate using optical absorption data. Surface morphology of sample is firm by Using Scanning electron microscopy (SEM) and the distribution of Zn, Cd, phosphate and oxygen species in the prepared sample is identified by EDS. PL studies recognize the white light emission. The 'g' value of the nanocomposite material synthesized is lesser than (negative shift) the free electron value (2.0023), which gives ionic nature to the bonding and confirms the presence of Mn2+ in distorted octahedral site symmetry.

  11. Redetermination of β-Ba(PO32

    Directory of Open Access Journals (Sweden)

    Matthias Weil

    2014-02-01

    Full Text Available In comparison with the previous structure determination of the β-modification of barium catena-polyphosphate that was based on Weissenberg film data [Grenier et al. (1967. Bull. Soc. Fr. Minéral. Cristallogr. 90, 24–31], the current CCD-data-based redetermination reveals all atoms with anisotropic displacement parameters, standard uncertainties for the atomic coordinates, and the determination of the absolute structure. Moreover, a much higher accuracy in terms of the bond-length distribution for the polyphosphate chain, with two shorter and two longer P—O distances, was achieved. The structure consists of polyphosphate chains extending parallel to [100] with a periodicity of two PO4 tetrahedra. The Ba2+ cations are located between the chains and are surrounded by ten O atoms in the form of a distorted coordination polyhedron, with Ba—O distances ranging from 2.765 (3 to 3.143 (3 Å, also reflecting the higher precision of the current redetermination.

  12. Luminescence properties of long-lasting phosphor SrMg2(PO4)2:Eu2+, Ho3+, Zr4+

    Science.gov (United States)

    Tang, Wei; Wang, Mingwen; Lin, Wei; Ye, Yaping; Wu, Xue

    2016-12-01

    Novel long lasting phosphors SrMg2(PO4)2:Eu2+, SrMg2(PO4)2:Eu2+, Zr4+, SrMg2(PO4)2:Eu2+, Ho3+ and SrMg2(PO4)2:Eu2+, Ho3+, Zr4+ were synthesized by conventional solid-state reaction method. The luminescent properties were systematically characterized by X-ray diffraction, photoluminescent excitation and emission spectra, as well as thermoluminescence spectrum and decay curves. The XRD patterns indicated that the samples belonged to monoclinic phase and co-doping Eu2+, Ho3+ and Zr4+ ions had no effect on the basic crystal structure. These phosphors emitting purplish blue light is related to the characteristic emission of Eu2+. The afterglow time of Eu2+ activated SrMg2(PO4)2 can be greatly enhanced by the co-doping of Ho3+, Zr4+. After the 365 nm UV light excitation source switching off, the Sr0.92Mg1.95(PO4)2:Eu2+0.01, Zr4+0.05, Ho3+0.07 phosphorescence can be observed for more than 1013 s in the limit of light perception of dark-adapted human eyes (0.32 mcd/m2). Different kinds of TL peaks at 423, 448 and 473 K have appeared, and traps densities have increased compared with the Eu2+ single doped SrMg2(PO4)2 phosphor. By analyzing the TL curve the depths of traps were calculated to be 0.846, 0.896 and 0.946 eV, respectively, which suggested that the co-doping of Ho3+, Zr4+ improved the electron storage ability of material. Besides, the mechanism was discussed in this report.

  13. LiFePO_4/C via fluoride doping

    Institute of Scientific and Technical Information of China (English)

    2012-01-01

    Non-stoichiometric compound fluoride-doped LiFePO4/C cathode materials were synthesized via solid-state reaction using MgF2 and AlF3 as dopant. The fluoride-doped LiFePO4/C samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and electrochemical testing. The results show that the materials are well crystallized and fluoride doping cannot change the space structure of LiFePO4. Slight amounts of Fe2O3 with no fluoride impurity were ...

  14. Discovery of the Cobalt Isotopes

    OpenAIRE

    Szymanski, T.; Thoennessen, M.

    2009-01-01

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

  15. Discovery of the Arsenic Isotopes

    CERN Document Server

    Shore, A; Heim, M; Schuh, A; Thoennessen, M

    2009-01-01

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

  16. poCAMon personal online continuous airmonitor; poCAMon online Personen Aerosolmonitor

    Energy Technology Data Exchange (ETDEWEB)

    Streil, T.; Oeser, V. [SARAD GmbH, Dresden (Germany)

    2015-07-01

    The poCAMon combines a very compact design with a high flow rate and long battery life. Its size and weight are still acceptable for carrying by one person. The unit measures long-lived aerosols as well as short-lived Radon/Thoron daughters by alpha spectroscopy and beta counting. The radioactive aerosols and particles are collected on the surface of a high resolution membrane filter. The alpha and beta decays on the filter are measured by a high-end semiconductor radiation detector (400 mm@). This allows a perfect separation of the different decay products. The increased pump rate (more than 3 l/ min) is suitable for lower detection limits. A sensor measures permanently the pressure drop on the filter in order to recognize an exhausted or perforated filter instantly. With the 3.8 Ah NiMH battery pack the poCAMon achieves an operation time of more than 30 hours. The quality control is a main issue of any radiation measurement. Therefore the poCAMon records a complete alpha spectrum for each measured value. This allows the monitoring of the device's perfect operation in each moment of the measurement. There are options for additional sensors for carbon monoxide and combustible gases as needed in underground mines. All measured data are stored in a 2GB memory card and can be accessed with a PC or laptop via a USB interface. Data transmission and device control can also be done via wireless ZigBee network or via a server for stationary operation with network access. A barometric pressure sensor and a GPS receiver are optional features of the device.

  17. Intracellular Cadmium Isotope Fractionation

    Science.gov (United States)

    Horner, T. J.; Lee, R. B.; Henderson, G. M.; Rickaby, R. E.

    2011-12-01

    Recent stable isotope studies into the biological utilization of transition metals (e.g. Cu, Fe, Zn, Cd) suggest several stepwise cellular processes can fractionate isotopes in both culture and nature. However, the determination of fractionation factors is often unsatisfactory, as significant variability can exist - even between different organisms with the same cellular functions. Thus, it has not been possible to adequately understand the source and mechanisms of metal isotopic fractionation. In order to address this problem, we investigated the biological fractionation of Cd isotopes within genetically-modified bacteria (E. coli). There is currently only one known biological use or requirement of Cd, a Cd/Zn carbonic anhydrase (CdCA, from the marine diatom T. weissfloggii), which we introduce into the E. coli genome. We have also developed a cleaning procedure that allows for the treating of bacteria so as to study the isotopic composition of different cellular components. We find that whole cells always exhibit a preference for uptake of the lighter isotopes of Cd. Notably, whole cells appear to have a similar Cd isotopic composition regardless of the expression of CdCA within the E. coli. However, isotopic fractionation can occur within the genetically modified E. coli during Cd use, such that Cd bound in CdCA can display a distinct isotopic composition compared to the cell as a whole. Thus, the externally observed fractionation is independent of the internal uses of Cd, with the largest Cd isotope fractionation occurring during cross-membrane transport. A general implication of these experiments is that trace metal isotopic fractionation most likely reflects metal transport into biological cells (either actively or passively), rather than relating to expression of specific physiological function and genetic expression of different metalloenzymes.

  18. In-Source Laser Spectroscopy with the Laser Ion Source and Trap: First Direct Study of the Ground-State Properties of ^{217,219}Po

    Directory of Open Access Journals (Sweden)

    D. A. Fink

    2015-02-01

    Full Text Available A Laser Ion Source and Trap (LIST for a thick-target, isotope-separation on-line facility has been implemented at CERN ISOLDE for the production of pure, laser-ionized, radioactive ion beams. It offers two modes of operation, either as an ion guide, which performs similarly to the standard ISOLDE resonance ionization laser ion source (RILIS, or as a more selective ion source, where surface-ionized ions from the hot ion-source cavity are repelled by an electrode, while laser ionization is done within a radio-frequency quadrupole ion guide. The first physics application of the LIST enables the suppression of francium contamination in ion beams of neutron-rich polonium isotopes at ISOLDE by more than 1000 with a reduction in laser-ionization efficiency of only 20. Resonance ionization spectroscopy is performed directly inside the LIST device, allowing the study of the hyperfine structure and isotope shift of ^{217}Po for the first time. Nuclear decay spectroscopy of ^{219}Po is performed for the first time, revealing its half-life, α-to-β-decay branching ratio, and α-particle energy. This experiment demonstrates the applicability of the LIST at radioactive ion-beam facilities for the production and study of pure beams of exotic isotopes.

  19. PHYSICOCHEMICAL PROPERTIES OF THE WATER DEPLETED OF HEAVY ISOTOPES

    Directory of Open Access Journals (Sweden)

    Vladislav V. Goncharuk

    2012-06-01

    Full Text Available Data on physicochemical properties of the light water (deuterium concentration is reduced to the ratio D/H = 4 ppm and that of the isotope of oxygen 18 – to the ratio 18O/16O = 750 ppm have been obtained. They include the melting and boiling points, kinematic viscosity, density, the spin-spin proton relaxation time, self-diffusion coefficients, and the small-angle laser light scattering. An explanation was proposed for the detected significant changes of the light water as compared with the high-resistivity water having geochemically ordinary isotope composition.

  20. Methodology for {sup 210}Po extraction from underground waters; Metodologia para a extracao de Po-210 em aguas subterraneas

    Energy Technology Data Exchange (ETDEWEB)

    Conceicao, Fabiano Tomazini da; Bonotto, Daniel Marcos [UNESP, Rio Claro, SP (Brazil). Inst. de Geociencias e Ciencias Exatas. Dept. de Petrologia e Metalogenia

    1998-07-01

    This work describes the first results obtained by the implementation of the methodology of {sup 210}Po extraction from underground waters. This methodology was first tested in the analysis of uranite sample from the Pocos de Caldas plateau (MG-Brazil) which constitutes a important natural source of {sup 210}Po. For the uranine sample a counting rate of 1.67 cpm for {sup 210}Po was obtained and for underground water 0.3 cpm was obtained which demonstrates that the used methodology is efficient for water analysis.

  1. Chromium isotope variations

    DEFF Research Database (Denmark)

    D'Arcy, Joan Mary

    is incorporated into carbonates. Hence, ancient carbonates can potentially record the Cr isotopic composition (δ53Cr ‰) of seawater in the geological past. Reliable application and interpretation of this proxy requires a detailed knowledge about processes that fractionate Cr on the Earth’s surface...... deposited during the Early Ordovician — a time of known redox instability in ancient oceans – exhibit a significant positive Cr isotope excursion of +0.5‰. This excursion is interpreted as the reductive drawn down of dissolved Cr in seawater in response to the development of a proximal anoxic sink......, and the quantification the Cr isotope composition of major Cr fluxes into and out of ocean. This thesis adds to the current knowledge of the Cr isotope system and is divided into two studies. The focus of the first study was to determine what processes control the Cr isotopic compositionof river water and to quantify...

  2. Isotopes in Greenland Precipitation

    DEFF Research Database (Denmark)

    Faber, Anne-Katrine

    Greenland ice cores offer a unique opportunity to investigate the climate system behaviour. The objective of this PhD project is to investigate isotope modelling of present- day conditions and conduct model-data comparison using Greenland ice cores. Thus this thesis investigates how the integration...... of model and data can be used to improve the understanding of climate changes. This is done through analysis of isotope modelling, observations and ice core measurements. This dissertation comprises three projects: (1) Modelling the isotopic response to changes in Arctic sea surface conditions, (2......) Constructing a new Greenland database of observations and present-day ice core measurements, and (3) Performance test of isotope-enabled CAM5 for Greenland. The recent decades of rapid Arctic sea ice decline are used as a basis for an observational-based model experiment using the isotope-enabled CAM model 3...

  3. Magnesium isotope fractionation during carbonatite magmatism at Oldoinyo Lengai, Tanzania

    Science.gov (United States)

    Li, Wang-Ye; Teng, Fang-Zhen; Halama, Ralf; Keller, Jörg; Klaudius, Jurgis

    2016-06-01

    To investigate the behaviour of Mg isotopes during carbonatite magmatism, we analyzed Mg isotopic compositions of natrocarbonatites and peralkaline silicate rocks from Oldoinyo Lengai, Tanzania. The olivine melilitites from the vicinity of Oldoinyo Lengai have homogeneous and mantle-like Mg isotopic compositions (δ26Mg of -0.30 to -0.26‰), indicating limited Mg isotope fractionation during mantle melting. The highly evolved peralkaline silicate rocks not related to silicate-carbonatite liquid immiscibility, including phonolites from the unit Lengai I, combeite-wollastonite nephelinites (CWNs) from the unit Lengai II A and carbonated combeite-wollastonite-melilite nephelinites (carbCWMNs), have δ26Mg values (from -0.25 to -0.10‰) clustered around the mantle value. By contrast, the CWNs from the unit Lengai II B, which evolved from the silicate melts that were presumably generated by silicate-carbonatite liquid immiscibility, have heavier Mg isotopes (δ26Mg of -0.06 to +0.09‰). Such a difference suggests Mg isotope fractionation during liquid immiscibility and implies, based on mass-balance calculations, that the original carbonatite melts at Lengai were isotopically light. The variable and positive δ26Mg values of natrocarbonatites (from +0.13 to +0.37‰) hence require a change of their Mg isotopic compositions subsequent to liquid immiscibility. The negative correlations between δ26Mg values and contents of alkali and alkaline earth metals of natrocarbonatites suggest Mg isotope fractionation during fractional crystallization of carbonatite melts, with heavy Mg isotopes enriched in the residual melts relative to fractionated carbonate minerals. Collectively, significant Mg isotope fractionation may occur during both silicate-carbonatite liquid immiscibility and fractional crystallization of carbonatite melts, making Mg isotopes a potentially useful tracer of these processes relevant to carbonatite petrogenesis.

  4. Microstructure and Properties of CePO4 Ceramic

    Institute of Scientific and Technical Information of China (English)

    WANG Lijuan; DU Haiyan; OU Xiujuan

    2006-01-01

    Cerium phosphate powders were synthesized by direct solid liquid reaction of cerium dioxide and phosphate acid at the Ce∶P ratio of 1∶1. Phase-pure and fine grain size CePO4 powers could be obtained by calcining the as received powders at the temperature higher than 600 ℃. It is demonstrated that the grain size and morphology of the CePO4 powders were calcined at various temperatures. An interesting layered crystal structure and a series of microcracks that cross and occur along the extrusion stress direction on the extruded surface inside CePO4 were observed. The ductility and machinabililty of CePO4 ceramic are attributed to the layered structure. Continuous machining debris was observed on the turned surface.

  5. Polonium 210Po in the phytobenthos from Puck Bay.

    Science.gov (United States)

    Skwarzec, B; Ulatowski, J; Strumińska, D I; Falandysz, J

    2003-04-01

    The aim of the work was to determine the 210Po content in phytobenthos species (seaweeds and angiosperms) from Puck Bay (southern Baltic). Alpha spectrometry was used to measure and calculate the activities and concentrations of polonium 210Po in the phytobenthos. The activity of 210Po in Puck Bay waters was determined to estimate the bioconcentration factors (BCF) of these plants. The 210Po concentration in water was estimated at 0.25 mBq dm(-3). The lowest polonium concentration in the phytobenthos was found in Cladophora rupestris (0.12 Bq kg(-1) wet wt.), the highest in Chara crinita (1.12 Bq kg(-1) wet wt.). Polonium is accumulated in these phytobenthos species; the bioconcentration factors (BCF) ranged from 450 to 4400.

  6. Chromium isotope fractionation during oxidative weathering of the Antrim Basalts: An insight into the global Cr geochemical cycle

    DEFF Research Database (Denmark)

    D'Arcy, Joan Mary; Døssing, Lasse Nørbye; Frei, Robert

    Cr isotopes fractionate during oxidative weathering of the continents; the oxidation of Cr (III) bearing minerals produces soluble Cr (VI) which is enriched in the heavy isotope, Cr (VI) is lost to local rivers resulting in a Cr depleted, isotopically light residual soil [1] [2]. To date, researc...

  7. Long-term sedimentary recycling of rare sulphur isotope anomalies.

    Science.gov (United States)

    Reinhard, Christopher T; Planavsky, Noah J; Lyons, Timothy W

    2013-05-01

    The accumulation of substantial quantities of O2 in the atmosphere has come to control the chemistry and ecological structure of Earth's surface. Non-mass-dependent (NMD) sulphur isotope anomalies in the rock record are the central tool used to reconstruct the redox history of the early atmosphere. The generation and initial delivery of these anomalies to marine sediments requires low partial pressures of atmospheric O2 (p(O2); refs 2, 3), and the disappearance of NMD anomalies from the rock record 2.32 billion years ago is thought to have signalled a departure from persistently low atmospheric oxygen levels (less than about 10(-5) times the present atmospheric level) during approximately the first two billion years of Earth's history. Here we present a model study designed to describe the long-term surface recycling of crustal NMD anomalies, and show that the record of this geochemical signal is likely to display a 'crustal memory effect' following increases in atmospheric p(O2) above this threshold. Once NMD anomalies have been buried in the upper crust they are extremely resistant to removal, and can be erased only through successive cycles of weathering, dilution and burial on an oxygenated Earth surface. This recycling results in the residual incorporation of NMD anomalies into the sedimentary record long after synchronous atmospheric generation of the isotopic signal has ceased, with dynamic and measurable signals probably surviving for as long as 10-100 million years subsequent to an increase in atmospheric p(O2) to more than 10(-5) times the present atmospheric level. Our results can reconcile geochemical evidence for oxygen production and transient accumulation with the maintenance of NMD anomalies on the early Earth, and suggest that future work should investigate the notion that temporally continuous generation of new NMD sulphur isotope anomalies in the atmosphere was likely to have ceased long before their ultimate disappearance from the rock record.

  8. Characteristics of brown carbon in the urban Po Valley atmosphere

    Science.gov (United States)

    Costabile, Francesca; Gilardoni, Stefania; Barnaba, Francesca; Di Ianni, Antonio; Di Liberto, Luca; Dionisi, Davide; Manigrasso, Maurizio; Paglione, Marco; Poluzzi, Vanes; Rinaldi, Matteo; Facchini, Maria Cristina; Gobbi, Gian Paolo

    2017-01-01

    We investigate optical-microphysical-chemical properties of brown carbon (BrC) in the urban ambient atmosphere of the Po Valley. In situ ground measurements of aerosol spectral optical properties, PM1 chemical composition (HR-ToF-AMS), and particle size distributions were carried out in Bologna. BrC was identified through its wavelength dependence of light absorption at visible wavelengths, as indicated by the absorption Ångström exponent (AAE). We found that BrC occurs in particles with a narrow monomodal size distribution peaking in the droplet mode, enriched in ammonium nitrate and poor in black carbon (BC), with a strong dependance on OA-to-BC ratios, and SSA530 of 0.98 ± 0.01. We demonstrate that specific complex refractive index values (k530 = 0.017 ± 0.001) are necessary in addition to a proper particle size range to match the large AAEs measured for this BrC (AAE467 - 660 = 3.2 ± 0.9 with values up to 5.3). In terms of consistency of these findings with literature, this study i. provides experimental evidence of the size distribution of BrC associated with the formation of secondary aerosol;ii. shows that in the lower troposphere AAE increases with increasing OA-to-BC ratios rather than with increasing OA - contributing to sky radiometer retrieval techniques (e.g., AERONET);iii. extends the dependence of AAE on BC-to-OA ratios previously observed in chamber experiments to ambient aerosol dominated by wood-burning emissions. These findings are expected to bear important implications for atmospheric modeling studies and remote sensing observations as regards the parametrization and identification of BrC in the atmosphere.

  9. Eudragit RS PO nanoparticles for sustained release of pyridostigmine bromide

    Energy Technology Data Exchange (ETDEWEB)

    Hoobakht, Fatemeh; Ganji, Fariba, E-mail: fganji@modares.ac.ir; Vasheghani-Farahani, Ebrahim [Tarbiat Modares University, Biomedical Engineering Group, Chemical Engineering Department (Iran, Islamic Republic of); Mousavi, Seyyed Mohammad [Tarbiat Modares University, Biotechnology Group, Chemical Engineering Department (Iran, Islamic Republic of)

    2013-09-15

    Pyridostigmine bromide (PB) is an inhibitor of cholinesterase, which is used in the treatment of myasthenia gravis and administered for protection against exposure to toxic nerve agents. Tests were done to investigate prolonging the half-life of PB and improving its release behavior. PB was loaded in nanoparticles (NPs) of Eudragit RS PO (Eu-RS) prepared using the technique of quasi emulsion solvent diffusion. Variables of output power of the sonicator, bath temperature and mixing time, were chosen as the optimization factors to obtain the minimum sized NPs. In addition, emulsions were tested at different ratios of drug-to-polymer by dynamic light scattering to determine size and zeta potential of NPs. UV-spectroscopy was used to determine PB content of the NPs. Drug-loaded NPs were characterized by scanning electron microscopy, X-ray diffraction, and Fourier transform infrared spectra. Results determined that mixing time had a significant impact on the size of Eu-RS NPs, but power output of sonicator and bath temperature had no significant effect. The particle size obtained at the optimum condition (power output of 70 W, bath temperature of 33 Degree-Sign C, and mixing time of 7 min) was less than 200 nm (optimum sizes were 138.9 and 179.5 nm for Eu-RS and PB-loaded Eu-RS NPs, respectively). The optimum PB-loaded Eu-RS NPs at the PB to Eu-RS weight ratio of 1-4 and 20 % of loaded PB released from the nanocarriers within 100 h.

  10. P.O. Box 196, Jimma, Ethiopia

    African Journals Online (AJOL)

    2003-11-11

    Nov 11, 2003 ... conditions that may produce such pictures are many. It is of great ... The variables incorporated in the structured report forms were ... of epithelial cells were visualized in lymph nodes (12). Suspicious ... diagnosed under light microscopy. Data analysis: ..... Torren, J.К. Human immunodeficiency virus and.

  11. Magnetic-luminescent YbPO4:Er,Dy microspheres designed for tumor theranostics with synergistic effect of photodynamic therapy and chemotherapy.

    Science.gov (United States)

    Wang, Wei; Xu, Dong; Wei, Xiaojun; Chen, Kezheng

    2014-01-01

    In this paper, magnetic and fluorescent bifunctional YbPO4:Er,Dy microspheres were synthesized via a simple solvothermal method. The prepared microspheres exposed to 980 nm near-infrared (NIR) laser light emitted bright upconversion fluorescence (450-570 nm) after calcination at high temperatures (>800°C). Results of magnetic resonance studies demonstrated that the YbPO4:Er,Dy microspheres are more suitable to be used as a transverse relaxation time (negative) contrast magnetic resonance imaging agent. The microspheres successfully entered the human hepatocellular carcinoma cells and presented low toxicity. A well-selected photodynamic therapy (PDT) drug, merocyanine 540 (MC540) with an ultraviolet-visible spectroscopy absorption maximum of 540 nm, was loaded onto the microspheres to obtain YbPO4:Er,Dy-MC540. Since the upconversion fluorescence emitting from the microspheres could be absorbed by MC540 with a small absorption/emission disparity, YbPO4:Er,Dy-MC540 could kill the hepatocellular carcinoma cells via PDT mechanism effectively. In other words, being upconverting particles, the prepared microspheres acted as light transducers in the NIR light-triggered PDT process. A chemotherapy drug, doxorubicin, was further loaded onto YbPO4:Er,Dy-MC540 to achieve enhanced antitumor effect based on synergistic therapeutic efficacy of PDT and chemotherapy. It is expected that the prepared YbPO4:Er,Dy microspheres have applications in tumor theranostics including magnetic-fluorescent bimodal imaging and NIR light-triggered PDT.

  12. The PoGOLite control system and software

    CERN Document Server

    Jackson, M S

    2013-01-01

    The autonomous control system of PoGOLite is presented. PoGOLite is a balloon borne X-ray polarimeter designed to observe point sources. To obtain scientific data with optimal efficiency, independent of the ground connection, the payload control system has been made autonomous in most functions. The overall system architecture and the interconnections between components, as well as the automation philosophy and software, are described. Results of performance tests are given.

  13. Stable isotope enrichment using a plasma centrifuge

    Science.gov (United States)

    Krishnan, Mahadevan; Bures, Brian; Madden, Robert

    2012-10-01

    A primary goal of the Department of Energy's Isotope Development and Production for Research and Applications Program (Isotope Program) within the Office of Nuclear Physics (NP) is to produce isotopes that are in short supply in the U.S. and of which there exists no or insufficient domestic commercial production capability. A vacuum arc plasma centrifuge is a rigid rotor column of metal plasma in which centrifugal forces re-distribute ions radially according to their mass/charge ratio. Early work demonstrated rotation at 2 million rpm and separation of various stable isotopes. The spinning plasma column had a Gaussian flux profile, peaked on the rigid rotor axis. This work adopts a more efficient approach, with the plasma created as a hollow column, wherein the flux is concentrated at larger radii where the centrifugal action is highest. By tailoring the vacuum arc discharge geometry, the rotation rate can also be increased to ˜10 million rpm. Data from Cu, Al and other metal plasmas will be presented and discussed in light of enriched stable isotopes needed for research and medicine.

  14. CERN to start producing medical isotopes

    CERN Multimedia

    Anaïs Schaeffer

    2012-01-01

    A promising project that was hailed at the ICTR-PHE 2012 medical conference (see Bulletin issues 10-11/2012 and 12-13/2012) has seen the light of day at CERN. The project, known by the name of MEDICIS, will make it possible to produce a large variety of radioactive isotopes for medical research.   This image of a brain, superimposed on a drawing by Leonardo da Vinci, was taken by a PET scanner after injecting a molecule containing a positron-emitting isotope. CERN-MEDICIS will produce new isotopes for imaging which will be able to show up cancerous tissues and destroy them by emitting local radiation as the isotopes decay. In the United States, a new radium-based drug which targets bone metastases is about to go on the market. Radium, which can be brought to bear at the cell level, is a potent weapon in the fight against certain types of cancer, and is opening the way to a new form of medicine. This is the direction that CERN has decided to follow through the CERN-MEDICIS* (Medical Isotopes...

  15. Improving rate performance of LiFePO{sub 4} cathode materials by hybrid coating of nano-Li{sub 3}PO{sub 4} and carbon

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Shi-Xi, E-mail: zhaosx@sz.tsinghua.edu.cn [Graduate School at Shenzhen, Tsinghua University, Shenzhen 518055 (China); Ding, Hao; Wang, Yan-Chao [Graduate School at Shenzhen, Tsinghua University, Shenzhen 518055 (China); School of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China); Li, Bao-Hua [Graduate School at Shenzhen, Tsinghua University, Shenzhen 518055 (China); Nan, Ce-Wen [School of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China)

    2013-07-25

    Highlights: •This paper reports an improved solid-state method which leads to a uniform coating. The influence of Li{sub 3}PO{sub 4} and carbon coating on the electrochemical performance of LiFePO{sub 4} was studied. •LiFePO{sub 4} coating with Li{sub 3}PO{sub 4} and carbon shows a higher capacity than pure carbon coating sample. •Results indicate that the surface structure has an important influence on the electrochemical performance of LiFePO{sub 4}. The addition of Li{sub 3}PO{sub 4} can decrease the interfacial resistance of Li FePO{sub 4}. -- Abstract: Li{sub 3}PO{sub 4} coating on the surface of LiFePO{sub 4} particles was prepared by direct dispersing LiFePO{sub 4} precursor in starch slurry with nano-Li{sub 3}PO{sub 4}. The existence of nano-Li{sub 3}PO{sub 4} was confirmed with X-ray powder diffraction (XRD). And the particle size and morphology were observed by scanning electron microscope (SEM) and transmission electron microscope analysis (TEM). The effects of the mixture coating on rate performance of LiFePO{sub 4} cathode vs Li anode at 25 °C was investigated. Li{sub 3}PO{sub 4} and carbon mixing coated LiFePO{sub 4} cathode materials exhibited markedly improved rate capability relative to bare carbon-coated LiFePO{sub 4}. Analyses on cell impedance showed that the Li{sub 3}PO{sub 4} coating decreased the interfacial impedance. Transmission electron microscope analysis, electrochemical impedance spectroscopy (EIS) and cyclic voltammograms (CV) were carried out to explain the reason of better rate performance by Li{sub 3}PO{sub 4} coating.

  16. Principles of failure probability assessment (PoF)

    Energy Technology Data Exchange (ETDEWEB)

    Giribone, R. [Bureau Veritas, Energy and Process Business Line, 17 bis Place des Reflets, Courbevoie 92400 (France); Valette, B. [Bureau Veritas, Energy and Process Business Line, 17 bis Place des Reflets, Courbevoie 92400 (France)]. E-mail: bernard.valette@bureauveritas.com

    2004-11-01

    This abstract presents a method for computing Probability of Failure (PoF) namely the method integrating the so-called 'Bayesian approach'. PoF along with the assessment of the consequences of failure are required when it comes to assessing 'risks'. More and more frequently, in modern industries, the trend is to rely on the use of risk-based approaches for the scheduling of the inspection of static pressure vessels. Equipment PoF is the main driver for scheduling periodical inspections. Within the Bayesian approach, it is expected that the performance of inspection, provided effective techniques are used, increases the knowledge we have on the equipment condition and help us gain confidence in the planning of future inspections. The paper thus describes the theoretical principles yielding to the calculation of the PoF prior to conduct an inspection and after its performance. PoF calculation within a Risk-Based Inspection (RBI) planning is one of the aspects covered by the EU project called 'RIMAP' (Risk-Based Inspection and Maintenance Procedure). PoF calculation using Bayes theorem is the cornerstone of the RBI methodology described in American Petroleum Institute reference 'API 581'.

  17. Investigation on Ductile Property of CePO4 Ceramic

    Institute of Scientific and Technical Information of China (English)

    王丽娟; 刘家臣; 王凯利; 霍伟荣; 高海

    2003-01-01

    Average grain size of chemicalty synthesized CePO4 powder increases with incre asing calcining temperature. The strength 184 Mpa and toughness 4.8 Mpa*m1/ 2 were achieved when the green compacts were sintered at 1500 ℃ for 2 h in air . They show that stepped or multilayered fracture occurs within CePO4 granules. CePO4 ceramic could be cut, drilled or turned easily using conventional metal-machining tools. Continuous machining debris was observed on turned surface. Indentation pressure stress-strain curve showes extensive nonlinear behavior, and a series of microcracks which crack cross and occur along the extrusion stre ss direction were observed on extruded surface, indicating single-phase CePO4 ceramic is "ductile". Based on the fracture analyses in cross-section surface, the ductility of CePO4 ceramic is considered to be associated with the cleavage of multilayered CePO4 grains and the fragment resetting to adapt to stress.

  18. Assessment of ²¹⁰Po in Italian diet.

    Science.gov (United States)

    Meli, Maria Assunta; Desideri, Donatella; Roselli, Carla; Feduzi, Laura

    2014-07-15

    This research was dedicated to the study, in the Italian daily diet, of the background activity concentration of (210)Po, a radionuclide with a high radiotoxicity. (210)Po was determined by alpha spectrometry. For food products of vegetable origin, the (210)Po activity concentration follows the trend: leafy vegetable>flour>rice>fruits>pasta>other vegetables>fruit vegetable; for those of animal origin: eggs>cheese>milk. The (210)Po activity concentration was also compared with that found by the same authors in meat, sea food, water and beverages in a previous study. The committed effective doses to individuals of three population groups (infants, children and adults) were 379, 222 and 151 μSv y(-1), respectively. The intake of foods of marine origin contributed about 67% of the total dose due to (210)Po ingestion. The effective dose, from (210)Po ingested by total diet, accounts for only 5-12% of the natural radiation exposure in Italy. Copyright © 2014 Elsevier Ltd. All rights reserved.

  19. Relational Aggression in Children with Preschool Onset (PO) Psychiatric Disorders

    Science.gov (United States)

    Belden, Andy C.; Gaffrey, Michael S.; Luby, Joan L.

    2012-01-01

    Objective The role of preschool onset (PO) psychiatric disorders as correlates and/or risk factors for relational aggression during kindergarten or 1st grade was tested in a sample of N = 146 preschool-age children (3 to 5.11). Method Axis-I diagnoses and symptom scores were derived using the Preschool Age Psychiatric Assessment. Children’s roles in relational aggression as aggressor, victim, aggressive-victim, or non-aggressor/non-victim were determined at preschool and again 24 months later at elementary school entry. Results Preschoolers diagnosed with PO-psychiatric disorders were 3 times as likely as the healthy preschoolers to be classified aggressors, victims, or aggressive-victims. Children diagnosed with PO-disruptive, depressive, and/or anxiety disorders were at least 6 times as likely as children without PO-psychiatric disorders to become aggressive-victims during elementary school after covarying for other key risk factors. Conclusions Findings suggested that PO-psychiatric disorders differentiated preschool and school-age children’s roles in relational aggression based on teacher-report. Recommendations for future research and preventative intervention aimed at minimizing the development of relational aggression in early childhood by identifying and targeting PO-psychiatric disorders are made. PMID:22917202

  20. Light Propagation Volumes

    OpenAIRE

    Mikulica, Tomáš

    2016-01-01

    Cílem diplomové práce je popsat různé metody výpočtu globálního osvětlení scény včetně techniky Light Propagation Volumes. Pro tuto metodu jsou podrobně popsány všechny tři kroky výpočtu: injekce, propagace a vykreslení. Dále je navrženo několik vlastních rozšíření zlepšující grafickou kvalitu metody. Části návrhu a implementace jsou zaměřeny na popis scény, zobrazovacího systému, tvorby stínů, implementace metody Light Propagation Volumes a navržených rozšíření. Práci uzavírá měření, porovná...

  1. Origin of magnetite in oxidized CV chondrites: in situ measurement of oxygen isotope compositions of Allende magnetite and olivine.

    Science.gov (United States)

    Choi, B G; McKeegan, K D; Leshin, L A; Wasson, J T

    1997-01-01

    Magnetite in the oxidized CV chondrite Allende mainly occurs as spherical nodules in porphyritic-olivine (PO) chondrules, where it is associated with Ni-rich metal and/or sulfides. To help constrain the origin of the magnetite, we measured oxygen isotopic compositions of magnetite and coexisting olivine grains in PO chondrules of Allende by an in situ ion microprobe technique. Five magnetite nodules form a relatively tight cluster in oxygen isotopic composition with delta 18O values from -4.8 to -7.1% and delta 17O values from -2.9 to -6.3%. Seven coexisting olivine grains have oxygen isotopic compositions from -0.9 to -6.3% in delta 18O and from -4.6 to -7.9% in delta 17O. The delta 17O values of the magnetite and coexisting olivine do not overlap; they range from -0.4 to -2.6%, and from -4.0 to -5.7%, respectively. Thus, the magnetite is not in isotopic equilibrium with the olivine in PO chondrules, implying that it formed after the chondrule formation. The delta 17O of the magnetite is somewhat more negative than estimates for the ambient solar nebula gas. We infer that the magnetite formed on the parent asteroid by oxidation of metal by H2O which had previously experienced minor O isotope exchange with fine-grained silicates.

  2. Matching isotopic distributions from metabolically labeled samples.

    Science.gov (United States)

    McIlwain, Sean; Page, David; Huttlin, Edward L; Sussman, Michael R

    2008-07-01

    In recent years stable isotopic labeling has become a standard approach for quantitative proteomic analyses. Among the many available isotopic labeling strategies, metabolic labeling is attractive for the excellent internal control it provides. However, analysis of data from metabolic labeling experiments can be complicated because the spacing between labeled and unlabeled forms of each peptide depends on its sequence, and is thus variable from analyte to analyte. As a result, one generally needs to know the sequence of a peptide to identify its matching isotopic distributions in an automated fashion. In some experimental situations it would be necessary or desirable to match pairs of labeled and unlabeled peaks from peptides of unknown sequence. This article addresses this largely overlooked problem in the analysis of quantitative mass spectrometry data by presenting an algorithm that not only identifies isotopic distributions within a mass spectrum, but also annotates matches between natural abundance light isotopic distributions and their metabolically labeled counterparts. This algorithm is designed in two stages: first we annotate the isotopic peaks using a modified version of the IDM algorithm described last year; then we use a probabilistic classifier that is supplemented by dynamic programming to find the metabolically labeled matched isotopic pairs. Such a method is needed for high-throughput quantitative proteomic metabolomic experiments measured via mass spectrometry. The primary result of this article is that the dynamic programming approach performs well given perfect isotopic distribution annotations. Our algorithm achieves a true positive rate of 99% and a false positive rate of 1% using perfect isotopic distribution annotations. When the isotopic distributions are annotated given 'expert' selected peaks, the same algorithm gets a true positive rate of 77% and a false positive rate of 1%. Finally, when annotating using machine selected peaks, which

  3. Study of polonium isotopes ground state properties by simultaneous atomic- and nuclear-spectroscopy

    CERN Multimedia

    Koester, U H; Kalaninova, Z; Imai, N

    2007-01-01

    We propose to systematically study the ground state properties of neutron deficient $^{192-200}$Po isotopes by means of in-source laser spectroscopy using the ISOLDE laser ion source coupled with nuclear spectroscopy at the detection setup as successfully done before by this collaboration with neutron deficient lead isotopes. The study of the change in mean square charge radii along the polonium isotope chain will give an insight into shape coexistence above the mid-shell N = 104 and above the closed shell Z = 82. The hyperfine structure of the odd isotopes will also allow determination of the nuclear spin and the magnetic moment of the ground state and of any identifiable isomer state. For this study, a standard UC$_{x}$ target with the ISOLDE RILIS is required for 38 shifts.

  4. DNA@Mn3(PO4)2 Nanoparticles Supported with Graphene Oxide as Photoelectrodes for Photoeletrocatalysis

    Science.gov (United States)

    Gao, Lixia; Xie, Jiale; Ma, Xiaoqing; Li, Man; Yu, Ling

    2017-01-01

    A novel deoxyribose nucleic acid (DNA)-based photoelectrode consisting of DNA@Mn3(PO4)2 nanoparticles on graphene oxide (GO) sheets was successfully fabricated for photoelectrocatalysis. DNA served as a soft template to guide the nucleation and growth of Mn3(PO4)2 nanoparticles in the synthesis of Mn3(PO4)2 nanoparticles. More importantly, the DNA also serves as semiconductor materials to adjust charge transport. Under UV light irradiation (180-420 nm, 15 mW/cm2), the photocurrent density of DNA@ Mn3(PO4)2/GO electrodes reached 9 μA/cm2 at 0.7 V bias (vs. SCE). An applied bias photon-to-current efficiency (ABPE) of 0.18% can be achieved, which was much higher than that of other control electrodes (DNA-based photoelectrode, well-matched energy levels can efficiently improve charge transfer and reduce the recombination of photogenerated electron-hole pairs.

  5. Strain-Induced Enhancement of Eu3+ Emission in Red Phosphor NaMgPO4:Eu3+, Al3+

    Science.gov (United States)

    Gao, Yong; Long, Qiwei; Nong, Rong; Wang, Tianman; Huang, Yingheng; Liao, Sen; Zhang, Huaxin

    2017-02-01

    A series of (NaMgPO4)0.98- x : {Eu}_{0.02}^{3 + }, {Al}x^{3 + } phosphors were prepared by the solid-state method. X-ray powder diffraction results confirm that the samples contain mixture phases of crystals. The doped effect of Al3+ on the photoluminescence properties of (NaMgPO4)0.98- x : {Eu}_{0.02}^{3 + }, {Al}x^{3 + } phosphors is discussed. The results indicate that two dependent curves of emission relative intensity and strain on Al3+ doping concentration are all Gaussian curves, and a high correlation is observed between emission relative intensity of Eu3+ and strain caused by Al3+. In other words, emission relative intensity of Eu3+ is enhanced with the increase of the strain. The enhanced mechanism of the strain is discussed. In addition, (NaMgPO4)0.98- x : {Eu}_{0.02}^{3 + }, {Al}x^{3 + } phosphors are electric dipole-dominated transition red phosphors. The optimal molar concentration of Al3+ for the samples is 9%, which (NaMgPO4)0.89: {Eu}_{0.02}^{3 + }, {Al}_{0.09}^{3 + } is a potential candidate as the red-emitting phosphor for ultraviolet-based white light-emitting diodes.

  6. Synthesis and luminescence of Eu(3+)-doped in triple phosphate Ca8MgBi(PO4)7 with whitlockite structure.

    Science.gov (United States)

    Zhang, Zhi-Wei; Ren, Yan-Jun; Liu, Lu; Zhang, Jian-Ping; Peng, You-Shun

    2015-12-01

    Triple whitlockite-type structure-based red phosphors Ca8 MgBi1-x(PO4)7:xEu(3+) (x = 0.10, 0.20, 0.30, 0.40, 0.50, 0.60, 0.70, 0.80 and 1.00) were synthesized by a conventional solid-state reaction route and characterized by their X-ray crystal structures. The X-ray diffraction (XRD) patterns, Fourier transform infrared spectra, morphologies, photoluminescence spectra, UV/Vis reflectance spectra, decay times and the International Commission on Illumination (CIE) chromaticity coordinates of Ca8MgBi1-x(PO4)7:xEu(3+) were analyzed. Eu-doped Ca8MgBi(PO4)7 phosphors exhibited strong red luminescence with peaks at 616 nm due to the (5)D0 → (7)F2 electric dipole transition of Eu(3+) ions after excitation at 396 nm. The UV/Vis spectra indicated that the band gap of Ca8MgBi0.30(PO4)7:0.70Eu(3+) is larger than that of Ca8MgBi(PO4)7. The phosphor developed in this study has great potential as a red-light-emitting phosphor for UV light-emitting diodes.

  7. Volatile and Isotopic Imprints of Ancient Mars

    Science.gov (United States)

    Mahaffy, Paul R.; Conrad, Pamela G.

    2015-01-01

    The science investigations enabled by Curiosity rover's instruments focus on identifying and exploring the habitability of the Martian environment. Measurements of noble gases, organic and inorganic compounds, and the isotopes of light elements permit the study of the physical and chemical processes that have transformed Mars throughout its history. Samples of the atmosphere, volatiles released from soils, and rocks from the floor of Gale Crater have provided a wealth of new data and a window into conditions on ancient Mars.

  8. Lighting: Green Light.

    Science.gov (United States)

    Maniccia, Dorine

    2003-01-01

    Explains that by using sustainable (green) building practices, schools and universities can make their lighting systems more efficient, noting that embracing green design principles can help schools attract students. Discusses lighting-control technologies (occupancy sensing technology, daylighting technology, and scheduling based technologies),…

  9. Preparation of TiO2-Ag3PO4 photocatalyst and its photocatalytic activity under UV irradiation%TiO2-Ag3PO4光催化剂的制备及其紫外光催化性能

    Institute of Scientific and Technical Information of China (English)

    李大军; 贺惠; 杨丽

    2016-01-01

    采用化学沉淀法(两步法)制备了TiO2-Ag3PO4复合光催化剂,考察了该光催化剂紫外光催化降解阳离子染料番红花红T(简称ST)的性能。实验结果表明:在TiO2-Ag3PO4投加量0.7 g/L、初始ST质量浓度70 mg/L、不调节溶液pH的条件下,紫外光照射35 min时的ST降解率高达97.9%;TiO2-Ag3PO4复合光催化剂的光催化性能明显优于单一光催化剂Ag3PO4和TiO2,同时也明显优于Ag-AgCl/Ag3PO4复合光催化剂;避光条件下反应40 min, TiO2-Ag3PO4对ST的吸附量仅为2.3 mg/g;TiO2-Ag3PO4在室内自然光下也具有一定的光催化活性;TiO2-Ag3PO4的光催化活性在酸性条件下要优于碱性条件;TiO2-Ag3PO4重复使用5次后,其光催化活性无明显下降,稳定性较好。%The TiO2-Ag3PO4 composite photocatalyst was prepared by chemical precipitation method(two-step method), and its photocatalytic activity under UV light to degradation of safranine T(ST)cationic dye was explored. The experimental results show that:Under the conditions of TiO2-Ag3PO4 dosage 0.7 g/L,initial ST mass concentration 70 mg/L,without pH adjustment and UV irradiation time 35 min,the degradation rate of ST is up to 97.9%;The photocatalytic activity of TiO2-Ag3PO4 is obviously higher than that of single photocatalyst Ag3PO4 and TiO2,and also Ag-AgCl/Ag3PO4 composite photocatalyst;The adsorption capacity of ST is only 2.3 mg/g after dark reaction for 40 min;TiO2-Ag3PO4 also has photocatalytic activity under indoor natural light;The photocatalytic activity of TiO2-Ag3PO4 in acidic condition is better than that in alkaline condition;TiO2-Ag3PO4 is stable with same photocatalytic activity after 5 times of reuse.

  10. PoV-GAME: PUNTOS DE VISTA MEDIANTE JUEGOS PoV-GAME: VIEWPOINTS THROUGH GAMES

    Directory of Open Access Journals (Sweden)

    Carlos Zapata-Jaramillo

    2012-06-01

    Full Text Available El desarrollo de proyectos de software considera importante la consistencia entre la información entregada por todos los interesados de una aplicación. En otras palabras, se procura llegar a acuerdos entre los diferentes puntos de vista de cada actor y llevarlos a cabo durante todo el proyecto. Con los métodos de enseñanza tradicionales se procura formar habilidades en este campo, pero no se afianzan mediante la práctica que, generalmente, se emplea para el aprendizaje en este campo. Por ello, en este artículo se propone ''PoV-GAME'', una nueva forma de ''jugar aprendiendo'', la cual busca fortalecer algunos conceptos básicos en la ingeniería de software como la consistencia en la información que se maneja a lo largo de un proyecto y afianzar la importancia de los puntos de vista en el desarrollo de un producto de software. Posteriormente, se analizan los resultados obtenidos luego de realizar el juego en diferentes grupos de estudiantes.Information for software applications is delivered by the stakeholders. Software development projects need consistency as an important aspect of such information. In other words, agreement among the different viewpoints must be reached in order to be implemented in the project. Well-known teaching methods try to create capabilities in this field, but they fail in reinforcing them in practice, which is commonly used for teaching in this field. Therefore, in this paper we propose ''PoV GAME'' a new way of ''play-to-learn''. We aim the reinforcement of some basic concepts about software engineering such as consistency in the information handled throughout the project, and the importance of viewpoints in the software product development. Subsequently, we analyze the results obtained after holding the game in several groups of students.

  11. Scatterometry Products Distributed by JPL PO.DAAC

    Science.gov (United States)

    Chen, R. L.; Lungu, T.; Benada, J. R.

    2001-12-01

    The Physical Oceanography Distributed Active Archive Center (PO.DAAC) at the Jet Propulsion Laboratory (JPL) archives and distributes physical oceanography data, including data from spacebased scatterometers. PO.DAAC's current archive contains more than six terabytes of scatterometry data, and PO.DAAC has distributed over 40 terabytes of that data to users worldwide. Those numbers increase steadily with the continuation of the QuikSCAT satellite, and that increase should effectively double with the pending launch of SeaWinds on ADEOS-II. The SeaWinds on QuikSCAT instrument provides the largest component of PO.DAAC's scatterometry data. Every day, the instrument makes 400,000 measurements and covers 90% of the ice-free oceans for wind data, with additional useful information over land and ice. PO.DAAC publicly distributes two QuikSCAT products: - Level 3 Daily, Gridded Ocean Wind Vectors (JPL SeaWinds Project) - Level 2B Ocean Wind Vectors in 25 Km Swath Grid (JPL SeaWinds Project) Scheduled to launch in February 2002, the SeaWinds on ADEOS-II instrument will provide a similar amount of data as QuikSCAT. PO.DAAC will again publicly distribute the level 2B and the level 3 products. Other scatterometry data currently available from PO.DAAC include: - BYU Daily Browse Images of QuikSCAT Sigma-0 Measurements (D. Long) - NSCAT Scatterometer ocean wind products - NSCAT Scatterometer Science Product, Levels 1.7, 2, 3 - NSCAT scatterometer global 25km sigma-0 and ocean winds (Dunbar) Samples of some of these datasets are presented.

  12. Comparison of electrochemical performances of olivine NaFePO4 in sodium-ion batteries and olivine LiFePO4 in lithium-ion batteries

    Science.gov (United States)

    Zhu, Yujie; Xu, Yunhua; Liu, Yihang; Luo, Chao; Wang, Chunsheng

    2012-12-01

    Carbon-coated olivine NaFePO4 (C-NaFePO4) spherical particles with a uniform diameter of ~80 nm are obtained by chemical delithiation and subsequent electrochemical sodiation of carbon-coated olivine LiFePO4 (C-LiFePO4), which is synthesized by a solvothermal method. The C-NaFePO4 electrodes are identical (particle size, particle size distribution, surface coating, and active material loading, etc.) to C-LiFePO4 except that Li ions in C-LiFePO4 are replaced by Na ions, making them ideal for comparison of thermodynamics and kinetics between C-NaFePO4 cathode in sodium-ion (Na-ion) batteries and C-LiFePO4 in lithium-ion (Li-ion) batteries. In this paper, the equilibrium potentials, reaction resistances, and diffusion coefficient of Na in C-NaFePO4 are systematically investigated by using the galvanostatic intermittent titration technique (GITT), electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV), and compared to those of the well-known LiFePO4 cathodes in Li-ion batteries. Due to the lower diffusion coefficient of Na-ion and higher contact and charge transfer resistances in NaFePO4 cathodes, the rate performance of C-NaFePO4 in Na-ion batteries is much worse than that of C-LiFePO4 in Li-ion batteries. However, the cycling stability of C-NaFePO4 is almost comparable to C-LiFePO4 by retaining 90% of its capacity even after 100 charge-discharge cycles at a charge-discharge rate of 0.1 C.Carbon-coated olivine NaFePO4 (C-NaFePO4) spherical particles with a uniform diameter of ~80 nm are obtained by chemical delithiation and subsequent electrochemical sodiation of carbon-coated olivine LiFePO4 (C-LiFePO4), which is synthesized by a solvothermal method. The C-NaFePO4 electrodes are identical (particle size, particle size distribution, surface coating, and active material loading, etc.) to C-LiFePO4 except that Li ions in C-LiFePO4 are replaced by Na ions, making them ideal for comparison of thermodynamics and kinetics between C-NaFePO4 cathode in

  13. Isotopes in Greenland Precipitation

    DEFF Research Database (Denmark)

    Faber, Anne-Katrine

    the Arctic Ocean. A comprehensive database is created based on ice core and weather station data from Greenland within the period 1890-2014. Present day annual and seasonal mean values are computed for 326 locations in Greenland. Parameterization of the spatial distribution of temperature and δ18O are used...... of model and data can be used to improve the understanding of climate changes. This is done through analysis of isotope modelling, observations and ice core measurements. This dissertation comprises three projects: (1) Modelling the isotopic response to changes in Arctic sea surface conditions, (2......) Constructing a new Greenland database of observations and present-day ice core measurements, and (3) Performance test of isotope-enabled CAM5 for Greenland. The recent decades of rapid Arctic sea ice decline are used as a basis for an observational-based model experiment using the isotope-enabled CAM model 3...

  14. Perchlorate isotope forensics

    Science.gov (United States)

    Böhlke, J.K.; Sturchio, N.C.; Gu, B.; Horita, J.; Brown, G.M.; Jackson, W.A.; Batista, J.; Hatzinger, P.B.

    2005-01-01

    Perchlorate has been detected recently in a variety of soils, waters, plants, and food products at levels that may be detrimental to human health. These discoveries have generated considerable interest in perchlorate source identification. In this study, comprehensive stable isotope analyses ( 37Cl/35Cl and 18O/17O/ 16O) of perchlorate from known synthetic and natural sources reveal systematic differences in isotopic characteristics that are related to the formation mechanisms. In addition, isotopic analyses of perchlorate extracted from groundwater and surface water demonstrate the feasibility of identifying perchlorate sources in contaminated environments on the basis of this technique. Both natural and synthetic sources of perchlorate have been identified in water samples from some perchlorate occurrences in the United States by the isotopic method. ?? 2005 American Chemical Society.

  15. Isotope Production Facility (IPF)

    Data.gov (United States)

    Federal Laboratory Consortium — The Los Alamos National Laboratory has produced radioactive isotopes for medicine and research since the mid 1970s, when targets were first irradiated using the 800...

  16. Calcium stable isotope geochemistry

    Energy Technology Data Exchange (ETDEWEB)

    Gausonne, Nikolaus [Muenster Univ. (Germany). Inst. fuer Mineralogie; Schmitt, Anne-Desiree [Strasbourg Univ. (France). LHyGeS/EOST; Heuser, Alexander [Bonn Univ. (Germany). Steinmann-Inst. fuer Geologie, Mineralogie und Palaeontologie; Wombacher, Frank [Koeln Univ. (Germany). Inst. fuer Geologie und Mineralogie; Dietzel, Martin [Technische Univ. Graz (Austria). Inst. fuer Angewandte Geowissenschaften; Tipper, Edward [Cambridge Univ. (United Kingdom). Dept. of Earth Sciences; Schiller, Martin [Copenhagen Univ. (Denmark). Natural History Museum of Denmark

    2016-08-01

    This book provides an overview of the fundamentals and reference values for Ca stable isotope research, as well as current analytical methodologies including detailed instructions for sample preparation and isotope analysis. As such, it introduces readers to the different fields of application, including low-temperature mineral precipitation and biomineralisation, Earth surface processes and global cycling, high-temperature processes and cosmochemistry, and lastly human studies and biomedical applications. The current state of the art in these major areas is discussed, and open questions and possible future directions are identified. In terms of its depth and coverage, the current work extends and complements the previous reviews of Ca stable isotope geochemistry, addressing the needs of graduate students and advanced researchers who want to familiarize themselves with Ca stable isotope research.

  17. Isotopically controlled semiconductors

    Energy Technology Data Exchange (ETDEWEB)

    Haller, E.E.

    2004-11-15

    A review of recent research involving isotopically controlled semiconductors is presented. Studies with isotopically enriched semiconductor structures experienced a dramatic expansion at the end of the Cold War when significant quantities of enriched isotopes of elements forming semiconductors became available for worldwide collaborations. Isotopes of an element differ in nuclear mass, may have different nuclear spins and undergo different nuclear reactions. Among the latter, the capture of thermal neutrons which can lead to neutron transmutation doping, can be considered the most important one for semiconductors. Experimental and theoretical research exploiting the differences in all the properties has been conducted and will be illustrated with selected examples. Manuel Cardona, the longtime editor-in-chief of Solid State Communications has been and continues to be one of the major contributors to this field of solid state physics and it is a great pleasure to dedicate this review to him.

  18. Isotopes through the looking glass

    Science.gov (United States)

    Mårtensson Pendrill, Ann Marie

    2000-08-01

    Nuclear distributions affect many aspects of atomic spectra. As an example, recent experimental results for the hyperfine anomaly in Fr isotopes are considered. These depend on nuclear charge and magnetization distributions. The variations in charge radii for these isotopes were studied earlier by measuring optical isotope shifts. The hyperfine anomalies for the odd-odd isotopes involve the neutron distributions, of interest for studies of parity nonconserving effects along a chain of isotopes.

  19. Methods of isotopic geochronology

    Science.gov (United States)

    Gorokhov, I. M.; Levchenkov, O. A.

    Papers are presented on such topics as the age of the chemical elements; the age of meteorites, the moon, and the earth; isotopic ages of the most ancient terrestrial formations; and the Archean evolution of Enderby Land in the Antarctic as evidenced by isotopic dating. Consideration is also given to a uranium-lead geochronology technique for investigating Precambrian ore deposits, a Pb-Pb technique of zircon dating, and the potentials and limitations of Sm-Nd geochronology.

  20. Comparison of electrochemical performances of olivine NaFePO4 in sodium-ion batteries and olivine LiFePO4 in lithium-ion batteries.

    Science.gov (United States)

    Zhu, Yujie; Xu, Yunhua; Liu, Yihang; Luo, Chao; Wang, Chunsheng

    2013-01-21

    Carbon-coated olivine NaFePO(4) (C-NaFePO(4)) spherical particles with a uniform diameter of ∼80 nm are obtained by chemical delithiation and subsequent electrochemical sodiation of carbon-coated olivine LiFePO(4) (C-LiFePO(4)), which is synthesized by a solvothermal method. The C-NaFePO(4) electrodes are identical (particle size, particle size distribution, surface coating, and active material loading, etc.) to C-LiFePO(4) except that Li ions in C-LiFePO(4) are replaced by Na ions, making them ideal for comparison of thermodynamics and kinetics between C-NaFePO(4) cathode in sodium-ion (Na-ion) batteries and C-LiFePO(4) in lithium-ion (Li-ion) batteries. In this paper, the equilibrium potentials, reaction resistances, and diffusion coefficient of Na in C-NaFePO(4) are systematically investigated by using the galvanostatic intermittent titration technique (GITT), electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV), and compared to those of the well-known LiFePO(4) cathodes in Li-ion batteries. Due to the lower diffusion coefficient of Na-ion and higher contact and charge transfer resistances in NaFePO(4) cathodes, the rate performance of C-NaFePO(4) in Na-ion batteries is much worse than that of C-LiFePO(4) in Li-ion batteries. However, the cycling stability of C-NaFePO(4) is almost comparable to C-LiFePO(4) by retaining 90% of its capacity even after 100 charge-discharge cycles at a charge-discharge rate of 0.1 C.

  1. Oxygen Isotopes in Meteorites

    Science.gov (United States)

    Clayton, R. N.

    2003-12-01

    Oxygen isotope abundance variations in meteorites are very useful in elucidating chemical and physical processes that occurred during the formation of the solar system (Clayton, 1993). On Earth, the mean abundances of the three stable isotopes are 16O: 99.76%, 17O: 0.039%, and 18O: 0.202%. It is conventional to express variations in abundances of the isotopes in terms of isotopic ratios, relative to an arbitrary standard, called SMOW (for standard mean ocean water), as follows:The isotopic composition of any sample can then be represented by one point on a "three-isotope plot," a graph of δ17O versus δ18O. It will be seen that such plots are invaluable in interpreting meteoritic data. Figure 1 shows schematically the effect of various processes on an initial composition at the center of the diagram. Almost all terrestrial materials lie along a "fractionation" trend; most meteoritic materials lie near a line of "16O addition" (or subtraction). (4K)Figure 1. Schematic representation of various isotopic processes shown on an oxygen three-isotope plot. Almost all terrestrial materials plot along a line of "fractionation"; most primitive meteoritic materials plot near a line of "16O addition." The three isotopes of oxygen are produced by nucleosynthesis in stars, but by different nuclear processes in different stellar environments. The principal isotope, 16O, is a primary isotope (capable of being produced from hydrogen and helium alone), formed in massive stars (>10 solar masses), and ejected by supernova explosions. The two rare isotopes are secondary nuclei (produced in stars from nuclei formed in an earlier generation of stars), with 17O coming primarily from low- and intermediate-mass stars (shielding in the UV photodissociation of CO (van Dishoeck and Black, 1988). This process results from the large differences in abundance between C16O, on the one hand, and C17O and C18O on the other. Photolysis of CO occurs by absorption of stellar UV radiation in the

  2. Jean Aicard et les Poèmes de Provence. Lecture rhétorique du poème liminaire

    Directory of Open Access Journals (Sweden)

    Michèle Gorenc

    2003-09-01

    Full Text Available Insistant sur l’influence de l’art oratoire sur l’œuvre poétique de Jean Aicard, l’article propose une lecture rhétorique du poème liminaire de son recueil Poèmes de Provence.

  3. Nickel and zinc isotope fractionation in hyperaccumulating and nonaccumulating plants.

    Science.gov (United States)

    Deng, Teng-Hao-Bo; Cloquet, Christophe; Tang, Ye-Tao; Sterckeman, Thibault; Echevarria, Guillaume; Estrade, Nicolas; Morel, Jean-Louis; Qiu, Rong-Liang

    2014-10-21

    Until now, there has been little data on the isotope fractionation of nickel (Ni) in higher plants and how this can be affected by plant Ni and zinc (Zn) homeostasis. A hydroponic cultivation was conducted to investigate the isotope fractionation of Ni and Zn during plant uptake and translocation processes. The nonaccumulator Thlaspi arvense, the Ni hyperaccumulator Alyssum murale and the Ni and Zn hyperaccumulator Noccaea caerulescens were grown in low (2 μM) and high (50 μM) Ni and Zn solutions. Results showed that plants were inclined to absorb light Ni isotopes, presumably due to the functioning of low-affinity transport systems across root cell membrane. The Ni isotope fractionation between plant and solution was greater in the hyperaccumulators grown in low Zn treatments (Δ(60)Ni(plant-solution) = -0.90 to -0.63‰) than that in the nonaccumulator T. arvense (Δ(60)Ni(plant-solution) = -0.21‰), thus indicating a greater permeability of the low-affinity transport system in hyperaccumulators. Light isotope enrichment of Zn was observed in most of the plants (Δ(66)Zn(plant-solution) = -0.23 to -0.10‰), but to a lesser extent than for Ni. The rapid uptake of Zn on the root surfaces caused concentration gradients, which induced ion diffusion in the rhizosphere and could result in light Zn isotope enrichment in the hyperaccumulator N. caerulescens. In high Zn treatment, Zn could compete with Ni during the uptake process, which reduced Ni concentration in plants and decreased the extent of Ni isotope fractionation (Δ(60)Ni(plant-solution) = -0.11 to -0.07‰), indicating that plants might take up Ni through a low-affinity transport system of Zn. We propose that isotope composition analysis for transition elements could become an empirical tool to study plant physiological processes.

  4. High-pressure optical floating-zone growth of Li(Mn,Fe)PO4 single crystals

    Science.gov (United States)

    Neef, Christoph; Wadepohl, Hubert; Meyer, Hans-Peter; Klingeler, Rüdiger

    2017-03-01

    Mm-sized LiMn1-xFexPO4 single crystals with 0 ⩽ x ⩽ 1 were grown by means of the traveling floating-zone technique at elevated Argon pressure of 30 bar. For the various doping levels, the growth process was optimized with respect to the composition-dependant effective light absorption and transparency of the materials. A convex crystal/melt interface, determined by the angle of incident light, was identified to be particularly crucial for a successful growth. The resulting large single crystalline grains are stoichiometric. Structure refinement shows that lattice parameters as well as the atomic positions and bond lengths linearly depend on the Mn:Fe-ratio. Oriented cuboidal samples with several mm3 of volume were used for magnetic studies which imply an antiferromagnetic ground state for all compositions. The Néel-temperature changes from TN = 32.5(5) K in LiMnPO4 to 49.5(5) K in LiFePO4 while the easy magnetic axis in the ordered phase flips from the crystallographic a- to the b-axis upon Fe-doping of x < 0.2 .

  5. Synthesis and Characterization of EO/PO Random Copolyethers

    Institute of Scientific and Technical Information of China (English)

    GUO Jian-guo; YUAN Ren-xu; HE Su-qin; ZHU Cheng-shen; JIAO Yu; JIANG Jian-ming

    2004-01-01

    Ethylene oxide(EO) and propylene oxide(PO) random copolyethers were synthesized by the sequential addition of the mixture of ethylene oxide and propylene oxide to propylene glycol (initiator) in the presence of potassium hydroxide(KOH), and characterized with infrared spectrum(FTIR) and nuclear magnetism resonance(NMR). The effects of catalyst concentration, reaction temperature, charging rate and EO/PO mixture ratio on the polymerization reaction were investigated. It was revealed that the optimal reaction condition is the ratio of 2.5:1000(KOH mass vs. product mass), at 114.6℃ and pressure below 0.4MPa. The residual KOH was neutralized by phosphoric acid(H3PO4). Then the crude copolyether was refined with adsorbents, and the refined copolyether, which contains less than 0.7μg/ml K+, was obtained as colorless, viscous liquid.

  6. Po-210 and other radionuclides in terrestrial and freshwater environments

    Energy Technology Data Exchange (ETDEWEB)

    Gjelsvik, Runhild; Brown, Justin (eds.) (Norwegian Radiation Protection Authority (Norway)); Holm, Elis (Univ. of Lund (Sweden)); Roos, Per (Risoe DTU (Denmark)); Saxen, Ritva; Outola, Iisa (STUK - Radiation and Nuclear Safety Authority (Finland))

    2009-01-15

    This report provides new information on Po-210 (and where appropriate its grandparent Pb-210) behaviour in environmental systems including humans. This has primarily been achieved through measurements of Po-210 in aquatic and terrestrial environments that has led to the derivation of information on the levels of this radioisotope in plants, animals and the biotic components of their habitat (i.e. water, soil) providing basic information on transfer where practicable. For freshwater environments, Po-210 concentration ratios derived for freshwater benthic fish and bivalve mollusc were substantially different to values collated from earlier review work. For terrestrial environments, activity concentrations of Po-210 in small mammals (although of a preliminary nature because no correction was made for ingrowth from Pb-210) were considerably higher than values derived from earlier data compilations. It was envisaged that data on levels of naturally occurring radionuclides would render underpinning data sets more comprehensive and would thus allow more robust background dose calculations to be performed subsequently. By way of example, unweighted background dose-rates arising from internal distributions of Po-210 were calculated for small mammals in the terrestrial study. The biokinetics of polonium in humans has been studied following chronic and acute oral intakes of selected Po radioisotopes. This work has provided information on gastrointestinal absorption factors and biological retention times thus improving the database upon which committed effective doses to humans are derived. The information generated in the report, in its entirety, should be of direct relevance for both human and non-human impact assessments. (au)

  7. Equilibrium and kinetic Si isotope fractionation factors and their implications on Si isotope distributions in the Earth's surface environments

    Science.gov (United States)

    Tang, M.; Zhang, S.; Liu, Y.

    2015-12-01

    Several important equilibrium Si isotope fractionation factors among minerals, organic molecules and the H4SiO4 solution are complemented to facilitate explanation of distributions of Si isotope in the Earth's surface environments. The results reveal that heavy Si isotopes will be significantly enriched in the secondary silicate minerals in comparison to aqueous H4SiO4. On the contrary, quadra-coordinated organosilicon complexes are enriched in light silicon isotope relative to the solution. The extent of 28Si-enrichment in hyper-coordinated organosilicon complexes is found the largest. In addition, the large kinetic isotope effect associated with the polymerization of monosilicic acid and dimer is calculated and the result supports previous statement that highly 28Si-enrichment in the formation of amorphous quartz precursor contributes to the discrepancy between theoretical calculations and field observations. With equilibrium Si isotope fractionation factors provided here, Si isotope distributions in many surface systems of the Earth can be explained. For example, the change of bulk soil δ30Si can be predicted as a concave pattern with respect to weathering degree, with the minimum value where allophane completely dissolves and the total amount of sesqui-oxides and poorly crystalline minerals reaches its maximum. When well-crystallized clays start to precipitate from pore solutions under equilibrium conditions, the bulk soil δ30Si will increase again and reach a constant value. Similarly, the precipitation of crystalline smectite and the dissolution of poorly crystalline kaolinite may explain δ30Si variations in the ground water profile. Equilibrium Si isotope fractionations among quadra-coordinated organosilicon complexes and the H4SiO4 solution may also shed the light on the Si isotope distributions in Si-accumulating plants.

  8. Facts and perceptions on the flood-risk evolution along the Po River

    Science.gov (United States)

    Domeneghetti, Alessio; Carisi, Francesca; Castellarin, Attilio

    2014-05-01

    Has the flood risk increased in the Po river basin during the last half century? The increasing frequency with which floods damages are recorded, or reported by media, strengthen the common perception that the flood risk is dramatically increasing in Europe and other areas of the world, due to a combination of different causes, among which climate change is often described as the major factor. However, there is a growing awareness of how anthropogenic pressures, such as uncontrolled urban and industrial expansion on flood-prone areas, may strongly impact the evolution of flood-risk in a given area, increasing potential flood damages and losses. Starting from these considerations, our study aims at shedding some light on the impact and relative importance of different factors controlling the flood risk. Focusing in particular on the middle-lower portion of the River Po, we analyse the evolution of flood hazard in the last half century referring to long streamflow series for different gauging stations located along the study reach (~450 km), while the modification of anthropogenic pressure is evaluated by referring to land-use and demographic dynamics observed from 1950s. Our study proposes simplified flood-vulnerability indices to be used for large scale flood-risk assessments and, on the basis of these indices, (1) we assess the importance of the different elements contributing to the definition of flood risk and (2) represent the evolution of flood risk in time along the middle and lower portion of the River Po. The results of the study represent an important piece of information that can be particularly useful to decision-makers in the definition of large scale flood-risk mitigation strategies and development plans for the study area.

  9. La solitude du poète touareg

    OpenAIRE

    Casajus, Dominique

    2004-01-01

    International audience; L'article traite de la poésie touarègue contemporaine, des sentiments qu'elle exprime ou qu'elle suscite, des voies par lesquelles elle se transmet. Il a paru dans les Actes d'un colloque tenu à l'Université libre de Bruxelles en 2001, et dédié aux variations du sentiment triste dans les musiques du monde et les poésies ou chansons populaires. Les styles de musique abordés étaient, entre autres, le blues, le fado, le flamenco, le tango, etc. Le trouble provoqué par cet...

  10. Po Superconducting Magnet:detail of the windings

    CERN Multimedia

    1982-01-01

    The Po superconducting dipole was built as a prototype beam transport magnet for the SPS extracted proton beam Po. Its main features were: coil aperture 72 mm, length 5 m, room-temperature yoke, NbTi cable conductor impregnated with solder, nominal field 4.2 T at 4.7 K (87% of critical field). It reached its nominal field without any quench. The photo shows a detail of the inner layer winding before superposing the outer layer to form the complete coil of a pole. Worth noticing is the interleaved glass-epoxy sheet (white) with grooved channels for the flow of cooling helium. See also 8307552X.

  11. Estrutura e discursividade do texto poético

    OpenAIRE

    Francisco de Assis Moura Sobreira

    2007-01-01

    Esta dissertação constitui uma investigação da estrutura e da discursividade do texto poético em suas virtualidades e está dividida em duas partes, distintas, mas não estanques. Na primeira parte, estudamos o texto poético considerando seus aspectos estruturais; na segunda, tratamos dos fatores que envolvem seus aspectos discursivos. Em relação aos os aspectos estruturais, consideramos o que formalmente torna o texto um objeto de arte literária. Aqui, em primeira mão, atentamos para os estudo...

  12. Structural and Electrochemical Characterization of Pure LiFePO4 and Nanocomposite C-LiFePO4 Cathodes for Lithium Ion Rechargeable Batteries

    OpenAIRE

    Arun Kumar(University of Delhi, Delhi, India); Thomas, R.; N. K. Karan; Saavedra-Arias, J. J.; M K Singh; Majumder, S. B.; Tomar, M. S.; Katiyar, R. S.

    2009-01-01

    Pure lithium iron phosphate (LiFePO4) and carbon-coated LiFePO4 (C-LiFePO4) cathode materials were synthesized for Li-ion batteries. Structural and electrochemical properties of these materials were compared. X-ray diffraction revealed orthorhombic olivine structure. Micro-Raman scattering analysis indicates amorphous carbon, and TEM micrographs show carbon coating on LiFePO4 particles. Ex situ Raman spectrum of C-LiFePO4 at various stages of charging and discharging showed reversibility upon...

  13. A novel route for FePO4 olivine synthesis from sarcopside oxidation

    Science.gov (United States)

    Crouzet, Camille; Recham, Nadir; Brunet, Fabrice; Findling, Nathaniel; David, Rénald; Sougrati, Moulay-Tahar

    2016-12-01

    Heterosite FePO4 is synthesized for the first time by direct thermal oxidation of sarcopside Fe3(PO4)2. Both FePO4 and Fe3(PO4)2 have a pseudo olivine structure. Complete isostructural conversion of sarcopside into FePO4 is achieved at a temperature of 450 °C within 3 days according to the reaction Fe3(PO4)2 + ¾ O2 → 2 FePO4 + ½ Fe2O3 which leads to the extraction of iron from the sarcopside structure. Appropriate heating ramp must be applied in order to avoid the crystallization of Fe7(PO4)6. Electrochemical performances of the oxidation product are consistent with those of olivine FePO4.

  14. Iron isotopes in an Archean ocean analogue

    Science.gov (United States)

    Busigny, Vincent; Planavsky, Noah J.; Jézéquel, Didier; Crowe, Sean; Louvat, Pascale; Moureau, Julien; Viollier, Eric; Lyons, Timothy W.

    2014-05-01

    Iron isotopes have been extensively used to trace the history of microbial metabolisms and the redox evolution of the oceans. Archean sedimentary rocks display greater variability in iron isotope ratios and more markedly negative values than those deposited in the Proterozoic and Phanerozoic. This increased variability has been linked to changes in either water column iron cycling or the extent of benthic microbial iron reduction through time. We tested these contrasting scenarios through a detailed study of anoxic and ferruginous Lac Pavin (France), which can serve as a modern analogue of the Archean ocean. A depth-profile in the water column of Lac Pavin shows a remarkable increase in dissolved Fe concentration (0.1-1200 μM) and δ56Fe values (-2.14‰ to +0.31‰) across the oxic-anoxic boundary to the lake bottom. The largest Fe isotope variability is found at the redox boundary and is related to partial oxidation of dissolved ferrous iron, leaving the residual Fe enriched in light isotopes. The analysis of four sediment cores collected along a lateral profile (one in the oxic layer, one at the redox boundary, one in the anoxic zone, and one at the bottom of the lake) indicates that bulk sediments, porewaters, and reactive Fe mostly have δ56Fe values near 0.0 ± 0.2‰, similar to detrital iron. In contrast, pyrite δ56Fe values in sub-chemocline cores (60, 65, and 92 m) are highly variable and show significant deviations from the detrital iron isotope composition (δ56Fepyrite between -1.51‰ and +0.09‰; average -0.93‰). Importantly, the pyrite δ56Fe values mirror the δ56Fe of dissolved iron at the redox boundary—where near quantitative sulfate and sulfide drawdown occurs—suggesting limited iron isotope fractionation during iron sulfide formation. This finding has important implications for the Archean environment. Specifically, this work suggests that in a ferruginous system, most of the Fe isotope variability observed in sedimentary pyrites can

  15. Frédéric Sylvanise. Langston Hughes, poète jazz, poète blues

    Directory of Open Access Journals (Sweden)

    Hélène CHRISTOL

    2011-03-01

    Full Text Available La Renaissance de Harlem a été redécouverte en France au début du XXIe siècle, grâce à l’organisation de manifestations publiques et universitaires ainsi que la publication de nombreuses études qui « revisitent » la période et les œuvres de ses écrivains et de ses artistes.  L’ouvrage de Frédéric Sylvanise, Langston Hughes, poète jazz, poète blues, publié par les éditions de l’ENS en 2009, apporte sa pierre à cet édifice critique puisqu’il se penche sur certains recueils de poésie de cet écri...

  16. Poétique de l’invective dans les Poèmes aristophanesques de Laurent Tailhade

    Directory of Open Access Journals (Sweden)

    Laurent Robert

    2012-04-01

    Full Text Available Parmi l’abondant corpus traité par Marc Angenot dans La Parole pamphlétaire, les ouvrages de Laurent Tailhade Au Pays du mufle et À travers les Grouins [sic] constituent les seuls recueils poétiques. L’essayiste y voit une illustration du genre de la satire poétique, revivifié dès la fin du xviiie siècle avec les Iambes d’André Chénier, puis au xixe notamment par Auguste Barbier et Victor Hugo. Tailhade pourrait ainsi, superficiellement, être considéré comme le poète satiriste de la Troisième...

  17. Structural and Electrochemical Characterization of Pure LiFePO4 and Nanocomposite C-LiFePO4 Cathodes for Lithium Ion Rechargeable Batteries

    Directory of Open Access Journals (Sweden)

    Arun Kumar

    2009-01-01

    Full Text Available Pure lithium iron phosphate (LiFePO4 and carbon-coated LiFePO4 (C-LiFePO4 cathode materials were synthesized for Li-ion batteries. Structural and electrochemical properties of these materials were compared. X-ray diffraction revealed orthorhombic olivine structure. Micro-Raman scattering analysis indicates amorphous carbon, and TEM micrographs show carbon coating on LiFePO4 particles. Ex situ Raman spectrum of C-LiFePO4 at various stages of charging and discharging showed reversibility upon electrochemical cycling. The cyclic voltammograms of LiFePO4 and C-LiFePO4 showed only a pair of peaks corresponding to the anodic and cathodic reactions. The first discharge capacities were 63, 43, and 13 mAh/g for C/5, C/3, and C/2, respectively for LiFePO4 where as in case of C-LiFePO4 that were 163, 144, 118, and 70 mAh/g for C/5, C/3, C/2, and 1C, respectively. The capacity retention of pure LiFePO4 was 69% after 25 cycles where as that of C-LiFePO4 was around 97% after 50 cycles. These results indicate that the capacity and the rate capability improved significantly upon carbon coating.

  18. Isotope geochemistry. Biological signatures in clumped isotopes of O₂.

    Science.gov (United States)

    Yeung, Laurence Y; Ash, Jeanine L; Young, Edward D

    2015-04-24

    The abundances of molecules containing more than one rare isotope have been applied broadly to determine formation temperatures of natural materials. These applications of "clumped" isotopes rely on the assumption that isotope-exchange equilibrium is reached, or at least approached, during the formation of those materials. In a closed-system terrarium experiment, we demonstrate that biological oxygen (O2) cycling drives the clumped-isotope composition of O2 away from isotopic equilibrium. Our model of the system suggests that unique biological signatures are present in clumped isotopes of O2—and not formation temperatures. Photosynthetic O2 is depleted in (18)O(18)O and (17)O(18)O relative to a stochastic distribution of isotopes, unlike at equilibrium, where heavy-isotope pairs are enriched. Similar signatures may be widespread in nature, offering new tracers of biological and geochemical cycling.

  19. Integrated Stable Isotope - Reactive Transport Model Approach for Assessment of Chlorinated Solvent Degradation

    Science.gov (United States)

    2016-05-01

    in the Deep Plume. .................................................... 25 Figure 6.4. C Isotope Ratios for TCE (red circles ), cDCE (light blue...Order Integral Degradation Rate Constants for TCE ( circles ), DCE (grey bars), and CEs Mineralization (black bars...for various CEs under different biogeochemical conditions • Isotope enrichment factors (ε) Contaminant Data • Decay chain for the contaminants of

  20. Research Update: Retardation and acceleration of phase separation evaluated from observation of imbalance between structure and valence in LiFePO4/FePO4 electrode

    Directory of Open Access Journals (Sweden)

    Kazuya Tokuda

    2014-07-01

    Full Text Available LiFePO4 is a potential positive electrode material for lithium ion batteries. We have experimentally observed an imbalance between the valence change of Fe ions and the structure change from the LiFePO4 phase to the FePO4 phase during delithiation by simultaneous in situ XRD and XANES measurements in an LiFePO4/FePO4 electrode. The ratio of structure change to valence change clearly indicates that the phase separation from LiFePO4 to FePO4 is suppressed at the beginning of delithiation, while it is accelerated at the latter stage, which is due to the coherent strain caused by the lattice misfit between the two phases.

  1. Magnetic relaxation in Zn(PO{sub 3}){sub 2}·Er(PO{sub 3}){sub 3} glass

    Energy Technology Data Exchange (ETDEWEB)

    Orendáč, M. [Institute of Physics, P.J. Šafárik University, Park Angelinum 9, 041 54 Košice (Slovakia); Tibenská, K. [Faculty of Aeronautics, Technical University, Rampová 7, 041 21 Košice (Slovakia); Čižmár, E.; Tkáč, V.; Orendáčová, A. [Institute of Physics, P.J. Šafárik University, Park Angelinum 9, 041 54 Košice (Slovakia); Holubová, J. [University of Pardubice, Faculty of Chemical Technology, Department of General and Inorganic Chemistry, Studentská 573, Pardubice 53210 (Czech Republic); Černošek, Z. [Institute of Physics, P.J. Šafárik University, Park Angelinum 9, 041 54 Košice (Slovakia); Faculty of Aeronautics, Technical University, Rampová 7, 041 21 Košice (Slovakia); University of Pardubice, Faculty of Chemical Technology, Department of General and Inorganic Chemistry, Studentská 573, Pardubice 53210 (Czech Republic); and others

    2016-08-15

    The results of experimental studies of alternating (ac) magnetic susceptibility and specific heat of Zn(PO{sub 3}){sub 2}·Er(PO{sub 3}){sub 3} glass are reported. Despite a high concentration of magnetic Er(III) ions the analysis of ac susceptibility ruled out the formation of a spin glass state in the used range of temperatures. Two relaxation processes were identified. The first one is thermally activated with a crossover in its temperature dependence observed at nominally 7 K. The relaxation at lower temperatures seems to be governed by a direct process with pronounced effect of phonon bottleneck. Striking deceleration of spin dynamics with increasing temperature found above 7 K is tentatively attributed to overcoming Ioffe – Regel crossover and strong scattering of acoustic phonons on local modes. Simplified prediction derived from a soft-mode-dynamics model confirms the presence of the boson peak observed in specific heat data and reasonably predicts the temperature of the crossover. The second process is consistent with a cross – tunneling relaxation. The obtained results suggest that magnetic doping of glasses and studying magnetic relaxation may represent an alternative tool for the investigation of lattice modes in glasses. - Highlights: • The boson peak in Zn(PO{sub 3}){sub 2}·Er(PO{sub 3}){sub 3} glass appears at temperatures, at which localized modes are thermally excited. • The formation of the boson peak is accompanied by anomalous slowing of the magnetic relaxation in Zn(PO{sub 3}){sub 2}·Er(PO{sub 3}){sub 3}.

  2. Online spectroscopy of trapped radium isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Versolato, Oscar O.; Giri, Gouri S.; Berg, Joost van den; Hoek, Duurt Johan van der; Kruithof, Wilbert; Santra, Bodhaditya; Shidling, Praveen; Willmann, Lorenz; Wilschut, Hans W.; Jungmann, Klaus [Kernfysisch Versneller Instituut, University of Groningen (Netherlands)

    2010-07-01

    Radium ions are of particular interest for a most precise measurement of Atomic Parity Violation. From a single cold and trapped ion one expects a significantly improved measurement of the weak mixing (Weinberg) angle through a determination of the light shift in the forbidden 7{sup 2}S{sub 1/2}-6{sup 2}D{sub 3/2} transition. In preparation of such precision measurements the transitions relevant for this (7S-7P, 6D-7P) were observed and measured in the isotopes {sup 212}Ra, {sup 213}Ra and {sup 214}Ra. The isotopes were produced at the TRI{mu}P facility of KVI, when a {sup 208}Pb beam hit a solid {sup 12}C target. The Ra isotopes were stopped and re-ionized to Ra{sup +} in a Thermal Ionizer, mass separated in a Wien Filter and cooled in a gas filled Radio Frequency Quadrupole. The ions were stored as a cloud in a Paul trap, where they also interacted with laser light. All necessary wavelengths were obtained by semiconductor lasers. The setup and the measurements will be discussed.

  3. Medical applications of Cu, Zn, and S isotope effects.

    Science.gov (United States)

    Albarede, Francis; Télouk, Philippe; Balter, Vincent; Bondanese, Victor P; Albalat, Emmanuelle; Oger, Philippe; Bonaventura, Paola; Miossec, Pierre; Fujii, Toshiyuki

    2016-10-01

    This review examines recent applications of stable copper, zinc and sulfur isotopes to medical cases and notably cancer. The distribution of the natural stable isotopes of a particular element among coexisting molecular species varies as a function of the bond strength, the ionic charge, and the coordination, and it also changes with kinetics. Ab initio calculations show that compounds in which a metal binds to oxygen- (sulfate, phosphate, lactate) and nitrogen-bearing moieties (histidine) favor heavy isotopes, whereas bonds with sulfur (cysteine, methionine) favor light isotopes. Oxidized cations (e.g., Cu(ii)) and low coordination numbers are expected to favor heavy isotopes relative to their reduced counterparts (Cu(i)) and high coordination numbers. Here we discuss the first observations of Cu, Zn, and S isotopic variations, three elements closely related along multiple biological pathways, with emphasis on serum samples of healthy volunteers and of cancer patients. It was found that heavy isotopes of Zn and to an even greater extent Cu are enriched in erythrocytes relative to serum, while the difference is small for sulfur. Isotopic variations related to age and sex are relatively small. The (65)Cu/(63)Cu ratio in the serum of patients with colon, breast, and liver cancer is conspicuously low relative to healthy subjects. The characteristic time over which Cu isotopes may change with disease progression (a few weeks) is consistent with both the turnover time of the element and albumin half-life. A parallel effect on sulfur isotopes is detected in a few un-medicated patients. Copper in liver tumor tissue is isotopically heavy. In contrast, Zn in breast cancer tumors is isotopically lighter than in healthy breast tissue. (66)Zn/(64)Zn is very similar in the serum of cancer patients and in controls. Possible reasons for Cu isotope variations may be related to the cytosolic storage of Cu lactate (Warburg effect), release of intracellular copper from cysteine

  4. Neutron diffraction studies of the Na-ion battery electrode materials NaCoCr2(PO4)3, NaNiCr2(PO4)3, and Na2Ni2Cr(PO4)3

    Science.gov (United States)

    Yahia, H. Ben; Essehli, R.; Avdeev, M.; Park, J.-B.; Sun, Y.-K.; Al-Maadeed, M. A.; Belharouak, I.

    2016-06-01

    The new compounds NaCoCr2(PO4)3, NaNiCr2(PO4)3, and Na2Ni2Cr(PO4)3 were synthesized by sol-gel method and their crystal structures were determined by using neutron powder diffraction data. These compounds were characterized by galvanometric cycling and cyclic voltammetry. NaCoCr2(PO4)3, NaNiCr2(PO4)3, and Na2Ni2Cr(PO4)3 crystallize with a stuffed α-CrPO4-type structure. The structure consists of a 3D-framework made of octahedra and tetrahedra that are sharing corners and/or edges generating channels along [100] and [010], in which the sodium atoms are located. Of significance, in the structures of NaNiCr2(PO4)3, and Na2Ni2Cr(PO4)3 a statistical disorder Ni2+/Cr3+ was observed on both the 8g and 4a atomic positions, whereas in NaCoCr2(PO4)3 the statistical disorder Co2+/Cr3+ was only observed on the 8g atomic position. When tested as negative electrode materials, NaCoCr2(PO4)3, NaNiCr2(PO4)3, and Na2Ni2Cr(PO4)3 delivered specific capacities of 352, 385, and 368 mA h g-1, respectively, which attests to the electrochemical activity of sodium in these compounds.

  5. Tunable multicolor and white luminescence in Tb{sup 3+}/Dy{sup 3+}/Mn{sup 2+} doped CePO{sub 4} via energy transfer

    Energy Technology Data Exchange (ETDEWEB)

    Yi, Zhigao [School of Materials Science and Engineering, Key Laboratory of Low-dimensional Materials and Application Technology (Ministry of Education), Xiangtan University, Xiangtan 411105 (China); Lu, Wei [University Research Facility in Materials Characterization and Device Fabrication, The Hong Kong Polytechnic University (Hong Kong); Zeng, Songjun, E-mail: songjunz@hunnu.edu.cn [College of Physics and Information Science and Key Laboratory of Low-dimensional Quantum Structures and Quantum Control of the Ministry of Education, Hunan Normal University, Changsha 410081, Hunan (China); Wang, Haibo; Rao, Ling [School of Materials Science and Engineering, Key Laboratory of Low-dimensional Materials and Application Technology (Ministry of Education), Xiangtan University, Xiangtan 411105 (China); Li, Zheng, E-mail: lizheng@xtu.edu.cn [School of Materials Science and Engineering, Key Laboratory of Low-dimensional Materials and Application Technology (Ministry of Education), Xiangtan University, Xiangtan 411105 (China)

    2015-07-15

    Highlights: • Tb{sup 3+}/Dy{sup 3+}/Mn{sup 2+} doped CePO{sub 4} DCNPs were prepared by a one-pot hydrothermal process. • The PL properties and the ET mechanism of these DCNPs were investigated in detail. • These DCNPs exhibit tunable multi-color output under UV excitation. • Intense white emissions can be realized by singly doping Dy{sup 3+} and Mn{sup 2+} in CePO{sub 4} host. - Abstract: In this paper, a series of Tb{sup 3+}/Dy{sup 3+}/Mn{sup 2+} doped CePO{sub 4} downconversion nanophosphors (DCNPs) were prepared by a one-pot hydrothermal process. The obtained DCNPs presented monoclinic and hexagonal phase structure with wire-like shape. The photoluminescence (PL) properties and the energy transfer (ET) mechanism of these DCNPs were investigated in detail. The ET mechanism of Ce{sup 3+}/Tb{sup 3+} in CePO{sub 4} host was calculated by means of concentration quenching and spectral overlapping, and calculation results revealed that dipole–dipole interactions should be more responsible. The maximum value of ET efficiency was measured to 87.4% for Tb{sup 3+} doped CePO{sub 4} system. In addition, owing to the efficient ET between Ce{sup 3+} and Tb{sup 3+}/Dy{sup 3+}/Mn{sup 2+}, these as-prepared DCNPs exhibit tunable multi-color output under ultra-violet (UV) light excitation. More importantly, the intense cold and warm white emissions can be realized by singly doping 2%Dy{sup 3+} and 20%Mn{sup 2+} in CePO{sub 4} host under UV irradiation, respectively. The corresponding CIE 1931 coordinates were calculated to be (0.30, 0.30) and (0.30, 0.32), respectively, which are closed to the standard white emission (0.33, 0.33). These findings demonstrate the efficient white light emission by singly doped Dy{sup 3+} or Mn{sup 2+} in CePO{sub 4} system for the first time, which is different from commonly used co-doped or tri-doped system. The multicolor tuning and white emission make these Tb{sup 3+}/Dy{sup 3+}/Mn{sup 2+} doped CePO{sub 4} DCNPs potential phosphors in

  6. Tuning photocatalytic performance of the near-infrared-driven photocatalyst Cu2(OH)PO4 based on effective mass and dipole moment.

    Science.gov (United States)

    Li, Zhujie; Dai, Ying; Ma, Xiangchao; Zhu, Yingtao; Huang, Baibiao

    2014-02-21

    Recently, Cu2(OH)PO4 was found as the first photocatalyst active in the near-infrared(NIR) region of the solar spectrum (Angew. Chem., Int. Ed., 2013, 52, 4810; Chem. Eng. News, 2013, 91, 36), motivating us to explore systemically its photocatalytic mechanism under near-infrared light and how to improve and tune its photocatalytic performance. Herein, electronic structures, and effective masses of electron and hole at energy band edges are theoretically investigated by employing spin-polarized density functional theory calculations. The calculated energy band structure supports the absorption spectra of Cu2(OH)PO4 in the NIR region corresponding to the electron excitation from the valence band to the unoccupied bands in the gap. Our charge density analysis indicates that the O atoms in the hydroxyl serves as the effective bridge for the favoring separation of the photogenerated electron-hole pairs. Furthermore, the effective masses of electron and hole analysis demonstrate that the separation and transfer of photogenerated carriers along the [011] direction may be more effective than other possible directions. A qualitative comparison of carrier transfer ability along all the directions in the specific planes is displayed by the three-dimensional band structure. Interestingly, the calculated net dipole moment for the two basic units of Cu2(OH)PO4, octahedron and trigonal bipyramid, indicate that the macroscopic dipole moment for Cu2(OH)PO4 is zero, however, the distorted octahedron unit has a net dipole moment, which enables us to tune the macroscopic dipole moment by doping. The present work provides theoretical insight leading to a better understanding of the photocatalytic performance of Cu2(OH)PO4 and it may be beneficial to prepare more efficient Cu2(OH)PO4 for NIR light photocatalysis, which will also be helpful to design and prepare novel photocatalysts.

  7. Stable isotopes. Applications and production; Les isotopes stables. Applications - production

    Energy Technology Data Exchange (ETDEWEB)

    Goldstein, S.; Louvet, P.; Soulie, E. [eds.

    1994-12-31

    This conference presents 46 communications concerning stable isotope production, utilization and application, grouped in 6 sessions and posters. The various themes are: biological applications (pharmacology, medical diagnosis, metabolism and protein studies, toxicity and response studies, labelled compounds), analysis procedures (NMR analysis for macromolecules, tracer studies), nuclear applications (utilization of stable isotopes in nuclear reactors), biological, physical and chemical applications (mass transfer, mobility, crystallography, isotopic exchange), stable isotope production (ion chromatography, ion cyclotron resonance, cryogenic distillation).

  8. Hydrothermal fabrication of multi-functional Eu3+ and Tb3+ co-doped BiPO4: Photocatalytic activity and tunable luminescence properties

    Science.gov (United States)

    Wang, Yao; Huang, Hongwei; Quan, Chaoming; Tian, Na; Zhang, Yihe

    2016-01-01

    We demonstrated for first time the tunable photoluminescence (PL) properties and photocatalytic activity of the Tb3+ and Eu3+ co-doped BiPO4 assemblies. They are fabricated via a facile hydrothermal approach. Through co-doping of Eu3+ and Tb3+ ions and changing the doping ratio, the emission color of the co-doped BiPO4 phosphors can be tuned precisely from green to yellow and red. Meanwhile, a very efficient energy transfer from Tb3+ to Eu3+ can be observed. Fascinatingly, a warmwhite color has been realized in the co-doped sample by tuning the ratio of Tb3+/Eu3+ to a certain value as displayed in the CIE chromaticity diagram. The doped BiPO4 samples also exhibit significantly enhanced photocatalytic activity compared to the pristine BiPO4 pertaining to Rhodamine (RhB) degradation under UV light. This enhancement should be attributed to the trapping electron effect induced by ion doping that endows BiPO4 with high separation of photoinduced electron-hole pairs, thereby greatly promoting the photocatalytic reactivity. It was corroborated by the electrochemical impedance spectra (EIS). Moreover, the crystal structure, microstructure and optical properties of as-prepared samples were investigated in details.

  9. The C3PO project: a laser communication system concept for small satellites

    Science.gov (United States)

    d'Humières, Benoît; Esmiller, Bruno; Gouy, Yann; Steck, Emilie; Quintana, Crisanto; Faulkner, Graham; O'Brien, Dominic; Sproll, Fabian; Wagner, Paul; Hampf, Daniel; Riede, Wolfgang; Salter, Michael; Wang, Qin; Platt, Duncan; Jakonis, Darius; Piao, Xiaoyu; Karlsson, Mikael; Oberg, Olof; Petermann, Ingemar; Michalkiewicz, Aneta; Krezel, Jerzy; Debowska, Anna; Thueux, Yoann

    2017-02-01

    The satellite market is shifting towards smaller (micro and nanosatellites), lowered mass and increased performance platforms. Nanosatellites and picosatellites have been used for a number of new, innovative and unique payloads and missions. This trend requires new concepts for a reduced size, a better performance/weight ratio and a reduction of onboard power consumption. In this context, disruptive technologies, such as laser-optical communication systems, are opening new possibilities. This paper presents the C3PO1 system, "advanced Concept for laser uplink/ downlink CommuniCation with sPace Objects", and the first results of the development of its key technologies. This project targets the design of a communications system that uses a ground-based laser to illuminate a satellite, and a Modulating Retro-Reflector (MRR) to return a beam of light modulated by data to the ground. This enables a downlink, without a laser source on the satellite. This architecture suits well to small satellite applications so as high data rates are potentially provided with very low board mass. C3PO project aims to achieve data rates of 1Gbit/s between LEO satellites and Earth with a communication payload mass of less than 1kilogram. In this paper, results of the initial experiments and demonstration of the key technologies will be shown.

  10. Superoutburst of WZ Sge-type dwarf nova below the period minimum: ASASSN-15po

    Science.gov (United States)

    Namekata, Kosuke; Isogai, Keisuke; Kato, Taichi; Littlefield, Colin; Matsumoto, Katsura; Kojiguchi, Naoto; Sugiura, Yuki; Uto, Yusuke; Fukushima, Daiki; Tatsumi, Taiki; Yamada, Eiji; Kamibetsunawa, Taku; de Miguel, Enrique; Stein, William L.; Sabo, Richard; Andreev, Maksim V.; Morelle, Etienne; Pavlenko, E. P.; Babina, Julia V.; Baklanov, Alex V.; Antonyuk, Kirill A.; Antonyuk, Okasana I.; Sosnovskij, Aleksei A.; Shugarov, Sergey Yu.; Golysheva, Polina Yu.; Gladilina, Natalia G.; Miller, Ian; Neustroev, Vitaly V.; Chavushyan, Vahram; Valdés, José R.; Sjoberg, George; Maeda, Yutaka; Itoh, Hiroshi; Masi, Gianluca; Michel, Raúl; Dubovsky, Pavol A.; Kiyota, Seiichiro; Tordai, Tamás; Oksanen, Arto; Ruiz, Javier; Nogami, Daisaku

    2017-02-01

    We report on a superoutburst of a WZ Sge-type dwarf nova (DN), ASASSN-15po. The light curve showed the main superoutburst and multiple rebrightenings. In this outburst, we observed early superhumps and growing (stage A) superhumps with periods of 0.050454(2) and 0.051809(13) d, respectively. We estimated that the mass ratio of secondary to primary (q) is 0.0699(8) by using Porb and a superhump period PSH of stage A. ASASSN-15po [Porb ˜ 72.6 min] is the first DN with an orbital period between 67-76 min. Although the theoretical predicted period minimum Pmin of hydrogen-rich cataclysmic variables (CVs) is about 65-70 min, the observational cut-off of the orbital period distribution at 80 min implies that the period minimum is about 82 min, and the value is widely accepted. We suggest the following four possibilities: the object is (1) a theoretical period minimum object, (2) a binary with a evolved secondary, (3) a binary with a metal-poor (Popullation II) seconday, or (4) a binary which was born with a brown-dwarf donor below the period minimum.

  11. Superoutburst of WZ Sge-type Dwarf Nova Below the Period Minimum: ASASSN-15po

    CERN Document Server

    Namekata, Kosuke; Kato, Taichi; Littlefield, Colin; Matsumoto, Katsura; Kojiguchi, Naoto; Sugiura, Yuki; Uto, Yusuke; Fukushima, Daiki; Tatsumi, Taiki; Yamada, Eiji; Kamibetsunawa, Taku; de Miguel, Enrique; Stein, William L; Sabo, Richard; Andreev, Maksim V; Morelle, Etienne; Pavlenko, E P; Babina, Julia V; Baklanov, Alex V; Antonyuk, Kirill A; Antonyuk, Okasana I; Sosnovskij, Aleksei A; Shugarov, Sergey Yu; Golysheva, Polina Yu; Gladilina, Natalia G; Miller, Ian; Neustroev, Vitaly V; Chavushyan, Vahram; Valdes, Jose R; Sjoberg, George; Maeda, Yutaka; Itoh, Hiroshi; Masi, Gianluca; Michel, Raul; Dubovsky, Pavol A; Kiyota, Seiichiro; Tordai, Tamas; Oksanen, Arto; Ruiz, Javier; Nogami, Daisaku

    2016-01-01

    We report on a superoutburst of a WZ Sge-type dwarf nova (DN), ASASSN-15po. The light curve showed the main superoutburst and multiple rebrightenings. In this outburst, we observed early superhumps and growing (stage A) superhumps with periods of 0.050454(2) and 0.051809(13) d, respectively. We estimated that the mass ratio of secondary to primary ($q$) is 0.0699(8) by using $P_{\\rm orb}$ and a superhump period $P_{\\rm SH}$ of stage A. ASASSN-15po [$P_{\\rm orb} \\sim$ 72.6 min] is the first DN with the orbital period between 67--76 min. Although the theoretical predicted period minimum $P_{\\rm min}$ of hydrogen-rich cataclysmic variables (CVs) is about 65--70 min, the observational cut-off of the orbital period distribution at 80 min implies that the period minimum is about 82 min, and the value is widely accepted. We suggest the following four possibilities: the object is (1) a theoretical period minimum object (2) a binary with a evolved secondary (3) a binary with a metal-poor (Popullation II) seconday (4) ...

  12. Deformation of C isotopes

    CERN Document Server

    Kanada-Enyo, Y

    2004-01-01

    Systematic analysis of the deformations of proton and neutron densities in even-even C isotopes was done based on the method of antisymmetrized molecular dynamics. The $E2$ transition strength was discussed in relation to the deformation. We analyze the $B(E2;2^+_1\\to 0^+_1)$ in $^{16}$C, which has been recently measured to be abnormally small. The results suggest the difference of the deformations between proton and neutron densities in the neutron-rich C isotopes. It was found that stable proton structure in C isotopes plays an important role in the enhancement the neutron skin structure as well as in the systematics of $B(E2)$ in the neutron-rich C.

  13. Isotopic characteristics of canopies in simulated leaf assemblages

    Science.gov (United States)

    Graham, Heather V.; Patzkowsky, Mark E.; Wing, Scott L.; Parker, Geoffrey G.; Fogel, Marilyn L.; Freeman, Katherine H.

    2014-11-01

    The geologic history of closed-canopy forests is of great interest to paleoecologists and paleoclimatologists alike. Closed canopies have pronounced effects on local, continental and global rainfall and temperature patterns. Although evidence for canopy closure is difficult to reconstruct from the fossil record, the characteristic isotope gradients of the "canopy effect" could be preserved in leaves and proxy biomarkers. To assess this, we employed new carbon isotopic data for leaves collected in diverse light environments within a deciduous, temperate forest (Maryland, USA) and for leaves from a perennially closed canopy, moist tropical forest (Bosque Protector San Lorenzo, Panamá). In the tropical forest, leaf carbon isotope values range 10‰, with higher δ13Cleaf values occurring both in upper reaches of the canopy, and with higher light exposure and lower humidity. Leaf fractionation (Δleaf) varied negatively with height and light and positively with humidity. Vertical 13C enrichment in leaves largely reflects changes in Δleaf, and does not trend with δ13C of CO2 within the canopy. At the site in Maryland, leaves express a more modest δ13C range (∼6‰), with a clear trend that follows both light and leaf height. Using a model we simulate leaf assemblage isotope patterns from canopy data binned by elevation. The re-sampling (bootstrap) model determined both the mean and range of carbon isotope values for simulated leaf assemblages ranging in size from 10 to over 1000 leaves. For the tropical forest data, the canopy's isotope range is captured with 50 or more randomly sampled leaves. Thus, with a sufficient number of fossil leaves it is possible to distinguish isotopic gradients in an ancient closed canopy forest from those in an open forest. For very large leaf assemblages, mean isotopic values approximate the δ13C of carbon contributed by leaves to soil and are similar to observed δ13Clitter values at forested sites within Panamá, including the

  14. Po kanalu TBTs pokazhut film o "Vaffen-SS"

    Index Scriptorium Estoniae

    2006-01-01

    Vene filmistuudio Treti Rim on tootnud lätivastase ajaloolise dokumentaali-propagandafilmi Teisest Maailmasõjast "Natslus Balti moodi" ("Natsizm po pribaltiski"). Filmi näitab täna Vene telekanal TVT, andes siiski võimaluse eetris esineda Läti Venemaa suursaadikule Andris Teikmanisele

  15. SrMnII2MnIII(PO43

    Directory of Open Access Journals (Sweden)

    Ghaleb Alhakmi

    2013-09-01

    Full Text Available The title compound, strontium trimanganese tris(orthophosphate, was synthesized under hydrothermal conditions. Its structure is isotypic to that of the lead analogue PbMnII2MnIII(PO43. Two O atoms are in general positions, whereas all others atoms are in special positions. The Sr and one P atom exhibit mm2 symmetry, the MnII atom 2/m symmetry, the MnIII atom and the other P atom .2. symmetry and two O atoms are located on mirror planes. The three-dimensional network of the crystal structure is made up of two types of chains running parallel to [010]. One chain is linear and is composed of alternating MnIIIO6 octahedra and PO4 tetrahedra sharing vertices; the other chain has a zigzag arrangement and is built up from two edge-sharing MnIIO6 octahedra connected to PO4 tetrahedra by edges and vertices. The two types of chains are linked through PO4 tetrahedra, leading to the formation of channels parallel to [100] and [010] in which the SrII ions are located. They are surrounded by eight O atoms in the form of a slightly distorted bicapped trigonal prism.

  16. PO.EX: Arquivo, Subarquivo, Meta-arquivo

    Directory of Open Access Journals (Sweden)

    Marques, Diogo

    2015-10-01

    Full Text Available Review of Rui TORRES & Sandy BALDWIN, PO.EX: Essays from Portugal on Cyberliterature and Intermedia (By Pedro Barbosa, Ana Hatherly and E. M. de Melo e Castro. Morgantown, WV: Center for Literary Computing, 2014, 282 pp. ISBN 978-1-938228-74-2

  17. Magnetic structure and magnetocalorics of GdPO4

    NARCIS (Netherlands)

    Palacios, E.; Rodriguez-Velamazan, J.A.; Evangelisti, M.; McIntyre, G.J.; Lorusso, G.; Visser, D.; De Jongh, L.J.; Boatner, L.A.

    2014-01-01

    The magnetic ordering structure of GdPO4 is determined at T=60 mK by the diffraction of hot neutrons with wavelength λ=0.4696 Å. It corresponds to a noncollinear antiferromagnetic arrangement of the Gd moments with propagation vector k=(1/2,0,1/2). This arrangement is found to minimize the dipole-di

  18. PoGOLite measurement of Crab polarisation and future plans

    Science.gov (United States)

    Pearce, Mark

    2016-07-01

    (For the PoGOLite Collaboration) The PoGOLite Pathfinder is a balloon-borne hard X-ray polarimeter designed for the observation of bright, ~1 Crab, sources. Polarisation is determined by measuring the azimuthal Compton scattering angle of incident X-rays in an array of plastic scintillators housed in an BGO anticoincidence well. The PoGOLite Pathfinder was launched from the SSC Esrange Space Centre in July 2013 resulting in a near-circumpolar flight of two weeks duration. The linear polarisation of hard X-ray emissions from the Crab was measured in a previously unexplored energy interval, 20-120 keV. The polarimetric response was characterised prior to flight using both polarised and unpolarised calibration sources. Systematic effects were addressed through observations of a background field. An upgraded polarimeter, PoGO+, is scheduled to fly in summer 2016 from Esrange. Results from the 2013 Pathfinder flight and prospects for the 2016 flight will be discussed.

  19. Recoil-deposited Po-210 in radon dwellings

    Energy Technology Data Exchange (ETDEWEB)

    Samuelsson, C.

    1990-12-31

    Short-lived decay products of Rn-222 plate out on all surfaces in a house containing radon gas. Following the subsequent alpha decays of the mother nuclei, the daughter products Pb-214 and Pb-210 are superficially and permanently absorbed. Due to its long half-life (22 y) the activity of absorbed Pb-210 accumulates in the surface. The activity of Pb-210, or its decay products, can thus reflect the past randon daughter and plate-out history of a house over several decades. Our results and experience from measurements of Po-210 and Rn-222 in 22 dwellings will be presented. In these studies the Po-210 surface activity of one plane glass sheet per dwelling (window panes were not used) has been determined and compared with the period of exposure times the mean radon concentration measured over a two-month period. Considering the large uncertainty in the integrated radon exposure estimate the surface {sup 210}Po correlates well (r=0.73) with the accumulated radon exposure. The {sup 210}Po activity of the glass samples has been measured non-destructively using an open-flow pulse ionization chamber and this detector has also been successfully applied in field exercises.

  20. Recoil-deposited Po-210 in radon dwellings

    Energy Technology Data Exchange (ETDEWEB)

    Samuelsson, C.

    1990-01-01

    Short-lived decay products of Rn-222 plate out on all surfaces in a house containing radon gas. Following the subsequent alpha decays of the mother nuclei, the daughter products Pb-214 and Pb-210 are superficially and permanently absorbed. Due to its long half-life (22 y) the activity of absorbed Pb-210 accumulates in the surface. The activity of Pb-210, or its decay products, can thus reflect the past randon daughter and plate-out history of a house over several decades. Our results and experience from measurements of Po-210 and Rn-222 in 22 dwellings will be presented. In these studies the Po-210 surface activity of one plane glass sheet per dwelling (window panes were not used) has been determined and compared with the period of exposure times the mean radon concentration measured over a two-month period. Considering the large uncertainty in the integrated radon exposure estimate the surface {sup 210}Po correlates well (r=0.73) with the accumulated radon exposure. The {sup 210}Po activity of the glass samples has been measured non-destructively using an open-flow pulse ionization chamber and this detector has also been successfully applied in field exercises.

  1. Bioaccumulation of polonium 210Po in marine birds.

    Science.gov (United States)

    Skwarzec, B; Fabisiak, J

    2007-01-01

    The aim of this work was to determine the 210Po content in marine birds which permanently or temporally live in the Polish part of the Baltic Sea. We chose 11 species of sea birds: three species permanently residing at southern Baltic Sea, four species of wintering birds and three species of migrating birds. The results show that the polonium is non-uniformly distributed in the marine birds. The highest activities of 210Po were observed in feathers, muscles and liver and the lowest in skin and skeleton. Species of birds that eat crustaceans, molluscs, fish and plants (long-tailed duck Clangula hyemalis, white-winged scoter Melanitta fusca) accumulated more polonium than species that eat mainly fish (great cormorant Phalacrocorax carbo, common guillemot Uria aalge) or plants (tufted duck Aythya fuligula). Moreover, about 63% of the 210Po that was located in feathers of razorbil (Alca torda) and long-tailed duck (C. hyemalis) was apparently adsorbed, suggesting an external source such as the air. It means that the adsorption of 210Po on the feather surface may be an important transfer from air to water.

  2. Polonium 210Po in cigarettes produced in Poland.

    Science.gov (United States)

    Skwarzec, B; Strumińska, D I; Borylo, A; Ulatowski, J

    2001-01-01

    This paper discusses the results of 210Po determinations in the fourteen most frequently smoked brands of cigarettes, which constitute over 80% of total cigarette consumption in Poland. The 210Po activity in the cigarette samples analysed (tobacco, ash, filter before and after smoking) were measured using alpha spectrometry (Canberra-Packard). The data indicates that there is considerable variation in the polonium content of these brands. The highest 210Po content per sample was found in the cheap "Popularne" brand (24.12 mBq), the lowest in "Caro" (4.23 mBq). There was also a large difference between the polonium remaining in the ash in comparison with its total content in the tobacco in all the brands (from 4.3% for "Golden American" to 71.0% for "Sobieski King-Size"). The analysis has demonstrated that filters absorbed only a small amount of the polonium contained in the tobacco. "Caro" cigarettes have the most efficient filter, retaining 25.1% of the polonium contained in the tobacco, but most filters absorbed only 0.1-7.2% of polonium. The daily inhalation of 210Po by Polish smokers who get through one pack per day ranges from 20 to 215 mBq, but people smoking two or more packs of "Popularne" brand will inhale over 430 mBq of polonium per day.

  3. Nuno Júdice: arte poética com melancolia

    Directory of Open Access Journals (Sweden)

    Ida Maria Santos Ferreira Alves

    2006-06-01

    Full Text Available Nuno Júdice é uma das mais representativas vozes no panorama poético de Portugal a partir da década de setenta, com uma escrita que tensiona os limites (limites? entre modernismo e pós-modernismo, configurando o que poderíamos nomear de uma poética da melancolia. O tom dessa poesia é freqüentemente pessimista; no entanto, essa afirmação deve ser relativizada porque, de fato, não é seu tom único, e sim expressão variável de diferentes sujeitos poéticos que vão aparecendo na cena do poema, representando um “drama em gente” a falar da condição humana no mundo contemporâneo, em meio a ruínas, fragmentos e vestígios da memória. Escrita perpassada de ironia, criticamente relendo a tradição poética ocidental, muitas vezes enfrenta a melancolia com um breve sorriso de quem sabe que o canto se faz de ficções e que é, apesar de sua desilusão, uma janela aberta, mirando o horizonte para além das ruínas deste mundo.

  4. 49 CFR 604.36 - Powers of a PO.

    Science.gov (United States)

    2010-10-01

    ... 49 Transportation 7 2010-10-01 2010-10-01 false Powers of a PO. 604.36 Section 604.36 Transportation Other Regulations Relating to Transportation (Continued) FEDERAL TRANSIT ADMINISTRATION... witnesses; and (k) Make findings of fact and conclusions of law and issue a recommended decision....

  5. Bioaccumulation of polonium {sup 210}Po in marine birds

    Energy Technology Data Exchange (ETDEWEB)

    Skwarzec, B. [University of Gdansk, Faculty of Chemistry, Chair of Analytical Chemistry, ul. Sobieskiego 18/19, 80-952 Gdansk (Poland)]. E-mail: bosk@chemik.chem.univ.gda.pl; Fabisiak, J. [Naval Academy, Smidowicza 61, 81-103 Gdynia (Poland)

    2007-07-01

    The aim of this work was to determine the {sup 210}Po content in marine birds which permanently or temporally live in the Polish part of the Baltic Sea. We chose 11 species of sea birds: three species permanently residing at southern Baltic Sea, four species of wintering birds and three species of migrating birds. The results show that the polonium is non-uniformly distributed in the marine birds. The highest activities of {sup 210}Po were observed in feathers, muscles and liver and the lowest in skin and skeleton. Species of birds that eat crustaceans, molluscs, fish and plants (long-tailed duck Clangula hyemalis, white-winged scoter Melanitta fusca) accumulated more polonium than species that eat mainly fish (great cormorant Phalacrocorax carbo, common guillemot Uria aalge) or plants (tufted duck Aythya fuligula). Moreover, about 63% of the {sup 210}Po that was located in feathers of razorbil (Alca torda) and long-tailed duck (C. hyemalis) was apparently adsorbed, suggesting an external source such as the air. It means that the adsorption of {sup 210}Po on the feather surface may be an important transfer from air to water.

  6. Isotopes in Condensed Matter

    CERN Document Server

    G Plekhanov, Vladimir

    2013-01-01

    This book provides a concise introduction to the newly created sub-discipline of solid state physics isotopetronics. The role of isotopes in materials and their properties are describe  in this book. The problem of the enigma of the atomic mass in microphysics is briefly discussed.  The range of the applications of isotopes is wide: from biochemical process in living organisms to modern technical applications in quantum information. Isotopetronics promises to improve nanoelectronic and optoelectronic devices. With numerous illustrations this book is useful to researchers, engineers and graduate students.

  7. Atomic Weights and Isotopic Compositions

    Science.gov (United States)

    SRD 144 Atomic Weights and Isotopic Compositions (Web, free access)   The atomic weights are available for elements 1 through 111, and isotopic compositions or abundances are given when appropriate.

  8. Development of a Portable Motor Learning Laboratory (PoMLab.

    Directory of Open Access Journals (Sweden)

    Ken Takiyama

    Full Text Available Most motor learning experiments have been conducted in a laboratory setting. In this type of setting, a huge and expensive manipulandum is frequently used, requiring a large budget and wide open space. Subjects also need to travel to the laboratory, which is a burden for them. This burden is particularly severe for patients with neurological disorders. Here, we describe the development of a novel application based on Unity3D and smart devices, e.g., smartphones or tablet devices, that can be used to conduct motor learning experiments at any time and in any place, without requiring a large budget and wide open space and without the burden of travel on subjects. We refer to our application as POrtable Motor learning LABoratory, or PoMLab. PoMLab is a multiplatform application that is available and sharable for free. We investigated whether PoMLab could be an alternative to the laboratory setting using a visuomotor rotation paradigm that causes sensory prediction error, enabling the investigation of how subjects minimize the error. In the first experiment, subjects could adapt to a constant visuomotor rotation that was abruptly applied at a specific trial. The learning curve for the first experiment could be modeled well using a state space model, a mathematical model that describes the motor leaning process. In the second experiment, subjects could adapt to a visuomotor rotation that gradually increased each trial. The subjects adapted to the gradually increasing visuomotor rotation without being aware of the visuomotor rotation. These experimental results have been reported for conventional experiments conducted in a laboratory setting, and our PoMLab application could reproduce these results. PoMLab can thus be considered an alternative to the laboratory setting. We also conducted follow-up experiments in university physical education classes. A state space model that was fit to the data obtained in the laboratory experiments could predict the

  9. Development of a Portable Motor Learning Laboratory (PoMLab).

    Science.gov (United States)

    Takiyama, Ken; Shinya, Masahiro

    2016-01-01

    Most motor learning experiments have been conducted in a laboratory setting. In this type of setting, a huge and expensive manipulandum is frequently used, requiring a large budget and wide open space. Subjects also need to travel to the laboratory, which is a burden for them. This burden is particularly severe for patients with neurological disorders. Here, we describe the development of a novel application based on Unity3D and smart devices, e.g., smartphones or tablet devices, that can be used to conduct motor learning experiments at any time and in any place, without requiring a large budget and wide open space and without the burden of travel on subjects. We refer to our application as POrtable Motor learning LABoratory, or PoMLab. PoMLab is a multiplatform application that is available and sharable for free. We investigated whether PoMLab could be an alternative to the laboratory setting using a visuomotor rotation paradigm that causes sensory prediction error, enabling the investigation of how subjects minimize the error. In the first experiment, subjects could adapt to a constant visuomotor rotation that was abruptly applied at a specific trial. The learning curve for the first experiment could be modeled well using a state space model, a mathematical model that describes the motor leaning process. In the second experiment, subjects could adapt to a visuomotor rotation that gradually increased each trial. The subjects adapted to the gradually increasing visuomotor rotation without being aware of the visuomotor rotation. These experimental results have been reported for conventional experiments conducted in a laboratory setting, and our PoMLab application could reproduce these results. PoMLab can thus be considered an alternative to the laboratory setting. We also conducted follow-up experiments in university physical education classes. A state space model that was fit to the data obtained in the laboratory experiments could predict the learning curves

  10. Reusable sunlight activated photocatalyst Ag{sub 3}PO{sub 4} and its significant antibacterial activity

    Energy Technology Data Exchange (ETDEWEB)

    Thiyagarajan, Shankar; Singh, Sarika; Bahadur, D., E-mail: dhirenb@iitb.ac.in

    2016-04-15

    A simple and surfactant free soft chemical approach is adopted for the successful synthesis of Ag{sub 3}PO{sub 4} nanoparticles (NPs) at room temperature. The obtained Ag{sub 3}PO{sub 4} NPs are nearly spherical in shape with a size of 250 ± 50 nm. These NPs are highly efficient for the degradation of three organic dyes (methylene blue, rhodamine B and methyl orange) under four different types of light sources. In this case, the superior photocatalytic activity is mainly driven by singlet oxygen radicals and it is confirmed through the electron spin resonance (ESR) spin trapping technique, using several quenchers/sources. Notably, these NPs have the ability to absorb large portion of solar spectrum and therefore it displays higher efficiency under sunlight as compared to UV-C light and a 60 W household compact fluorescence lamp (CFL). Furthermore, these NPs exhibit excellent colloidal stability and recycling capability for the degradation of dyes. In addition, it possesses significant antibacterial activity with complete inhibition of bacterial pathogen, Escherichia coli at a very low concentration (0.01 mg/mL) after a mere 15 min of incubation time. The inhibition of bacterial growth is also suggested from the generation of intracellular reactive oxygen species (ROS) in E. coli by fluorescence microscopy. Thus, these NPs may provide a potential outcome for the environmental remediation. - Graphical abstract: Schematic representation of the mechanism involved in photodegradation of organic dyes and inhibition of bacterial growth using Ag{sub 3}PO{sub 4} nanoparticles. - Highlights: • Excellent catalytic activity for dyes degradation under different light sources. • Mechanism involving catalyst mediated ROS generation in photocatalysis suggested. • Good recycling capability of Ag{sub 3}PO{sub 4} even after the fifth cycles. • Extraordinary antibacterial activity of Ag{sub 3}PO{sub 4} after a very short incubation time. • Detection of intracellular

  11. Crystal structure and luminescence property of a novel blue-emitting Cs2xCa2xGd2(1-x)(PO4)2:Eu(2+) (x = 0.36) phosphor.

    Science.gov (United States)

    Geng, Kang; Xia, Zhiguo; Molokeev, Maxim S

    2014-10-07

    A novel blue-emitting double-phosphate phosphor Cs0.72Ca0.72Gd1.28(PO4)2:Eu(2+) was synthesized by the sol-gel method, and the structure and luminescence properties were investigated in detail. The crystal structure and chemical composition of Cs0.72Ca0.72Gd1.28(PO4)2 matrix was analyzed and determined based on Rietveld refinements and phase and chemical composition analysis. The composition-optimized Cs0.72Ca0.72Gd1.28(PO4)2:Eu(2+) exhibited strong blue light, peaking at 462 nm upon excitation at 365 nm with the CIE coordinates of (0.139, 0.091). The quenching concentration of Eu(2+) in the Cs0.72Ca0.72Gd1.28(PO4)2 phase was about 0.01 and attributed to the dipole-quadrupole interaction. The thermally stable luminescence properties, fluorescence decay curves and diffuse reflectance spectra of Cs0.72Ca0.72Gd1.28(PO4)2:Eu(2+) phosphors are also discussed, all of which indicate that the Cs0.72Ca0.72Gd1.28(PO4)2:Eu(2+) phosphor is a promising phosphor for application in white-light UV LEDs.

  12. Deformation and mixing of co-existing shapes in the neutron-deficient polonium isotopes

    CERN Document Server

    AUTHOR|(CDS)2078559; Huyse, Mark

    The neutron-deficient polonium isotopes, with only 2 protons outside the Z = 82 shell closure, are situated in an interesting region of the nuclear chart. In the neighboring lead (Z = 82) and mercury (Z = 80) isotopes, experimental and theoretical efforts identified evidence of shape coexistence. Shape coexistence is the remarkable phenomenon in which two or more distinct types of deformation occur in states of the same angular momentum and similar excitation energy in a nucleus. The neutron-deficient polonium isotopes have also been studied intensively, experimentally as well as theoretically. The closed neutron-shell nucleus 210Po (N = 126) manifests itself as a two-particle nucleus where most of the excited states can be explained by considering the degrees of freedom of the two valence protons outside of 208Pb. The near-constant behavior of the yrast 2+1 and 4+1 states in the isotopes with mass 200 ≤ A ≤ 208 can be explained by coupling the two valence protons to a vibrating lead core. 200Po seems to ...

  13. Discoveries of isotopes by fission

    Indian Academy of Sciences (India)

    M Thoennessen

    2015-09-01

    Of the about 3000 isotopes presently known, about 20% have been discovered in fission. The history of fission as it relates to the discovery of isotopes as well as the various reaction mechanisms leading to isotope discoveries involving fission are presented.

  14. NASA's Planetary Science E/PO Forum: Reflections on Five Years of Effort to Support an E/PO Community

    Science.gov (United States)

    Shipp, S. S.; Shebby, S.; Buxner, S.; Boonstra, D.; Cobabe-Ammann, E. A.; Cobb, W. H.; Dalton, H.; Grier, J.; Klug Boonstra, S. L.; LaConte, K.; Ristvey, J.; Shupla, C. B.; Weeks, S.; Wessen, A. S.; Zimmerman-Brachman, R.

    2014-12-01

    Over the past decade, NASA's Science Mission Directorate (SMD) has funded four education and public outreach (E/PO) forums, aligned with each of its science divisions, including Astrophysics, Earth Science, Heliophysics, and Planetary Science. Together, these forums help organize individual division E/PO programs into a coordinated, effective, efficient, nationwide effort that shares the scientific discoveries of NASA across a broad array of audiences. In the past four-and-a-half years, the Planetary Science Division's Forum - in collaboration with the other three Forums - has worked to support its community of education professionals and scientists involved in E/PO to communicate, collaborate, and strengthen their efforts. The Forum's work encompasses identification of best practices based on educational research, increasing understanding of needs through audience-based working groups, the development of strategic collaborations and partnerships to increase programmatic reach, and the creation of strategic resources to support community members in their E/PO work (e.g., an online workspace for the community to communicate, collaborate, and share practices; recommendations to scientists for increasing impact in educational settings; a one-stop shop for NASA SMD classroom and informal education products, http://nasawavelength.org). Drawing on evaluation data, the presentation will explore what resources and support mechanisms are valued by the community, ways the community uses the available resources, and the outcomes of the effort to date.

  15. A synthesis of LiFePO{sub 4} starting from FePO{sub 4} under reducing atmosphere

    Energy Technology Data Exchange (ETDEWEB)

    Prosini, Pier Paolo [ENEA, Italian National Agency for New Technologies, Energy and Sustainable Economic Development, Casaccia Research Centre, Via Anguillarese 301, 00123 Santa Maria di Galeria, Rome, Italy and DInESto, Drive the Innovation in Energy Storage, Via Provin (Italy); Cento, Cinzia; Masci, Amedeo; Carewska, Maria; Gislon, Paola [ENEA, Italian National Agency for New Technologies, Energy and Sustainable Economic Development, Casaccia Research Centre, Via Anguillarese 301, 00123 Santa Maria di Galeria, Rome (Italy)

    2014-06-19

    A fast and easy way to produce LiFePO{sub 4} starting from FePO{sub 4}, used as iron and phosphorus source, is proposed. 5% hydrogen is employed as a reducing agent and various compounds containing lithium as lithiation agents. The selected lithiation agents included: LiCl, CH{sub 3}COOLi, LiOH, Li{sub 2}S, LiH, and Li{sub 2}CO{sub 3}. Solid state synthesis is used for the LiFePO{sub 4} preparation and the so obtained materials are structurally characterized by XRD. The materials are used to fabricate composite electrode and their specific capacity is evaluated by low rate galvanostatic charge/discharge cycles (C/10 rate). Among the various lithium salts, the acetate give rise to the LiFePO{sub 4} with the best electrochemical performance. The morphology of this material is further investigated by SEM microscopy and the specific capacity is evaluated as a function of the discharge rate and the cycle number.

  16. Combustion synthesis and luminescence properties of LaPO4: Eu (5%)

    Institute of Scientific and Technical Information of China (English)

    Mounir Ferhi; Karima Horchani-Naifer; Mokhtar Férid

    2009-01-01

    Rare earth doped materials are an important type of phosphors due to their excellent performance such as stability at high tem-perature and light emission covering the entire visible domain. The combustion synthesis at acid pH of the monoclinic LaPO4: Eu(5%) pow-sis was followed by structure, morphology characterisation and luminescent properties of the obtained compound. The room temperature emission measurements under ultraviolet excitation at 254 nm were made for the emission transition 5D0→7FJ of this phosphor. The CIE (Commission Internationale de L'Eclairage) chromatic coordinates, dominant wavelength and colour purity were determined and compared to other luminescent materials obtained by other methods.

  17. ComPoScan: Adaptive Scanning for Efficient Concurrent Communications and Positioning with 802.11

    DEFF Research Database (Denmark)

    King, Thomas; Kjærgaard, Mikkel Baun

    2008-01-01

    active scanning to allow positioning and to minimize the impact on the data flow. The system is configurable to realize different trade-offs between position accuracy and the level of communication interruption. We provide extensive experimental results by emulation on data collected at several sites......Using 802.11 concurrently for communications and positioning is problematic, especially if location-based services (e.g., indoor navigation) are concurrently executed with real-time applications (e.g., VoIP, video conferencing). Periodical scanning for measuring the signal strength interrupts...... the data flow. Reducing the scan frequency is no option because it hurts the position accuracy. For this reason, we need an adaptive technique to mitigate this problem. This work proposes ComPoScan which, based on movement detection, adaptively switches between light-weight monitor sniffing and invasive...

  18. Organic carbon isotopes of the Sinian and Early Cambrian black shales on Yangtze Platform, China

    Institute of Scientific and Technical Information of China (English)

    李任伟; 卢家烂; 张淑坤; 雷加锦

    1999-01-01

    Organic matter of the Sinian and early Cambrian black shales on the Yangtze Platform belongs to the light carbon group of isotopes with the δ13C values from - 27 % to -35 % , which are lower than those of the contemporaneously deposited carbonates and phosphorites. A carbon isotope-stratified paleooceanographic model caused by upwelling is proposed, which can be used not only to interpret the characteristics of organic carbon isotopic compositions of the black shales, but also to interpret the paleogeographic difference in the organic carbon isotope compositions of various types of sedimentary rocks.

  19. The synthesis and luminescence properties of a novel red-emitting phosphor: Eu3+-doped Ca9La(PO4)7

    Science.gov (United States)

    Liang, Zehui; Mu, Zhongfei; Wang, Qiang; Zhu, Daoyun; Wu, Fugen

    2017-10-01

    A series of novel red-emitting phosphors Ca9La1- x (PO4)7: xEu3+ were synthesized by high-temperature solid state reactions. The photoluminescence excitation and photoluminescence spectra of these phosphors were investigated in detail. O2--Eu3+ charge transfer band peaking at about 261 nm is dominant in the PLE spectra of Eu3+-doped Ca9La(PO4)7, indicating that the phosphors are suitable for tricolor fluorescent lamps. The phosphors also show a good absorption in near ultraviolet (around 395 nm) and blue (around 465 nm) spectral region, which indicates that it can be pumped with NUV and blue chips for white light-emitting diodes. The transition of 5D0 → 7F2 of Eu3+ in this lattice can emit bright red light. Ca9La(PO4)7 could accommodate a large amount of Eu3+ with an optimal concentration of 60 mol%. The dipole-dipole interaction between Eu3+ is the dominant mechanism for concentration quenching of Eu3+. The calculated color coordinates lie in red region ( x = 0.64, y = 0.36), which is close to Y2O3: 0.05Eu3+ ( x = 0.65, y = 0.34). The integral emission intensity of Ca9La0.4(PO4)7: 0.6Eu3+ is 1.9 times stronger than that of widely used commercial red phosphor Y2O3: 0.05Eu3+. All these results indicate that Eu3+-doped Ca9La(PO4)7 is a promising red-emitting phosphor which can be used in tricolor fluorescent lamps and white light-emitting diodes.

  20. GEOCHRONOMETRY ISOTOPE GEOLOGY

    Institute of Scientific and Technical Information of China (English)

    2004-01-01

    <正>20040631 Chen Jiangfeng (School of Earth and Space Sciences, University of Science and Technology of China, Hefei, Anhui) ; Xie Zhi Relationships Between Rb-Sr, Ar - Ar Geochronometers and Oxygen Isotopic Equilibrium of Intrusions from Eastern Anhui Province, China (Geological Journal of China Universities, ISSN 1006 - 7493, CN 32 -

  1. GEOCHRONOMETRY & ISOTOPE GEOLOGY

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    <正>20090432 Zhou Shuqing (School of Energy Resources, China University of Geosciences Beijing 100083, China); Huang Haiping Stable Isotopic Records vs. Important Events in Life Evolution and the Concurrent Environment (Geological Review, ISSN0371-5736, CN11-1952, 54(2), 2008, p.225-231, 3 illus., 1 table, 77 refs.)

  2. GEOCHRONOMETRY & ISOTOPE GEOLOGY

    Institute of Scientific and Technical Information of China (English)

    2014-01-01

    <正>20141014Wang Hairan(State Key Laboratory of Continental Dynamics,Department of Geology,Northwest University,Xi’an710069,China);Zhao Hongge Theory and Application of Zircon U-Pb Isotope Dating Technique(Geology and Resources,ISSN1671-1947,CN21-1458/P,22(3),2013,p.229

  3. GEOCHRONOMETRY & ISOTOPE GEOLOGY

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    <正>20072750 Huang Sijing(State Key Laboratory of Oil/Gas Reservoir Geology and Exploitation,Chengdu University of Technology,Chengdu 610059,China);Pei Changrong Age Calibration for the Boundary between Lower and Middle Triassic by Strontium Isotope Stratigraphy in Eastern Sichuan Province

  4. GEOCHRONOMETRY & ISOTOPE GEOLOGY

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    <正>20070454 Bao Zengkuan (Institute of High Energy Physics, CAS, Beijing 100049, China); Yuan Wanming Apatite (U-Th)/He Dating and Its Application (Acta Petrologica et Mineralogica, ISSN1000-6524, CN11-1966/P, 24(2), 2005, p.126-132, 2 illus., 25 refs.) Key words: isotopic geochronology

  5. Isotopic Implicit Surface Meshing

    NARCIS (Netherlands)

    Boissonnat, Jean-Daniel; Cohen-Steiner, David; Vegter, Gert

    2004-01-01

    This paper addresses the problem of piecewise linear approximation of implicit surfaces. We first give a criterion ensuring that the zero-set of a smooth function and the one of a piecewise linear approximation of it are isotopic. Then, we deduce from this criterion an implicit surface meshing algor

  6. Isotope hydrograph separation

    Energy Technology Data Exchange (ETDEWEB)

    Fritz, P. [UFZ-Umweltforschungszentrum, Centre of Environmental Research Leipzig-Halle, Leipzig (Germany)

    2000-07-01

    Storm-runoff thus reflects the complex hydraulic behaviour of drainage basins and water-links of such systems. Water of different origin may participate in the events and in this lecture, the application of isotope techniques to separate storm hydrographs into different components will be presented.

  7. Forensic Stable Isotope Biogeochemistry

    Science.gov (United States)

    Cerling, Thure E.; Barnette, Janet E.; Bowen, Gabriel J.; Chesson, Lesley A.; Ehleringer, James R.; Remien, Christopher H.; Shea, Patrick; Tipple, Brett J.; West, Jason B.

    2016-06-01

    Stable isotopes are being used for forensic science studies, with applications to both natural and manufactured products. In this review we discuss how scientific evidence can be used in the legal context and where the scientific progress of hypothesis revisions can be in tension with the legal expectations of widely used methods for measurements. Although this review is written in the context of US law, many of the considerations of scientific reproducibility and acceptance of relevant scientific data span other legal systems that might apply different legal principles and therefore reach different conclusions. Stable isotopes are used in legal situations for comparing samples for authenticity or evidentiary considerations, in understanding trade patterns of illegal materials, and in understanding the origins of unknown decedents. Isotope evidence is particularly useful when considered in the broad framework of physiochemical processes and in recognizing regional to global patterns found in many materials, including foods and food products, drugs, and humans. Stable isotopes considered in the larger spatial context add an important dimension to forensic science.

  8. Reactivity of NH{sub 4}H{sub 2}PO{sub 4} toward LaCl{sub 3} in LiCl-KCl Melt Flux. Step by Step Formation of Monazite-Like LaPO{sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Hudry, D.; Jobic, St.; Deniard, Ph. [Univ Nantes, CNRS, Inst Mat Jean Rouxel, F-44322 Nantes 3 (France); Hudry, D.; Bardez, I.; Bart, F. [CEA Marcoule, DTCD SECM LDMC, 30 (France); Rakhmatullin, A.; Bessada, C. [CNRS, CEM HTI, F-45071 Orleans 2 (France); Rakhmatullin, A.; Bessada, C. [Univ Orleans, Fac Sci, F-45067 Orleans 2 (France)

    2009-08-15

    The synthesis of lanthanum phosphates in molten LiCl-KCl eutectic was chosen to address the preliminary treatment of chlorinated wastes containing fission products that are already present in a Li/Cl eutectic. The obtained monazite compound shows interesting properties to be considered as a good candidate to trap lanthanum for a long-time. The synthesis route based on LaCl{sub 3} reaction with NH{sub 4}H{sub 2}PO{sub 4} in a stoichiometric amount is a key point to obtain monazite as a pure phase. Hence, the salt composition is not modified during the synthesis reaction. The chemical reactivity of ammonium dihydrogenphosphate (NH{sub 4}H{sub 2}PO{sub 4}, hereafter abbreviated ADP) toward lanthanum chloride (LaCl{sub 3}) in molten LiCl-KCl eutectic is probed by NMR spectroscopy to follow the formation of LaPO{sub 4}. Formally, a direct transformation of the two aforementioned precursors into LaPO{sub 4}, NH{sub 4}Cl and HCl can be discarded on the basis of the low thermal stability of ADP. To shed some light on the formation of LaPO{sub 4}, in situ and ex situ NMR experiments were carried out on LiCl-KCl/LaCl{sub 3}/ADP, as well as LiCl-KCl/ADP, KCl/ADP, and LiCl/ADP mixtures. First, the reactivity of the precursors in contact with the eutectic was studied from room temperature to 600 degrees C by means of {sup 31}P, {sup 35}Cl, and {sup 139}La high temperature NMR. Second, ex situ room temperature magic angle spinning (MAS) and Radiofrequency driven recoupling (RFDR) {sup 31}P solid-state NMR experiments were carried out on solid samples prepared in different conditions (i.e., temperature and atmosphere) and quenched at room temperature to identify frozen intermediate species in their metastable state. On the basis of this approach, we propose a model for the LaPO{sub 4} formation based on a multistep mechanism which highlights the strong reactivity of ADP toward the alkaline salts but without final change in the composition of the solvent. (authors)

  9. Reactivity of NH4H2PO4 toward LaCl3 in LiCl-KCl melt flux. Step by step formation of monazite-like LaPO4.

    Science.gov (United States)

    Hudry, Damien; Rakhmatullin, Aydar; Bessada, Catherine; Bardez, Isabelle; Bart, Florence; Jobic, Stéphane; Deniard, Philippe

    2009-08-03

    The synthesis of lanthanum phosphates in molten LiCl-KCL eutectic was chosen to address the preliminary treatment of chlorinated wastes containing fission products that are already present in a Li/Cl eutectic. The obtained monazite compound shows interesting properties to be considered as a good candidate to trap lanthanum for a long-time. The synthesis route based on LaCl(3) reaction with NH(4)H(2)PO(4) in a stoichiometric amount is a key point to obtain monazite as a pure phase. Hence, the salt composition is not modified during the synthesis reaction. The chemical reactivity of ammonium dihydrogenphosphate (NH(4)H(2)PO(4), hereafter abbreviated ADP) toward lanthanum chloride (LaCl(3)) in molten LiCl-KCl eutectic is probed by NMR spectroscopy to follow the formation of LaPO(4). Formally, a direct transformation of the two aforementioned precursors into LaPO(4), NH(4)Cl and HCl can be discarded on the basis of the low thermal stability of ADP. To shed some light on the formation of LaPO(4), in situ and ex situ NMR experiments were carried out on LiCl-KCl/LaCl(3)/ADP, as well as LiCl-KCl/ADP, KCl/ADP, and LiCl/ADP mixtures. First, the reactivity of the precursors in contact with the eutectic was studied from room temperature to 600 degrees C by means of (31)P, (35)Cl, and (139)La high temperature NMR. Second, ex situ room temperature magic angle spinning (MAS) and RadioFrequency driven recoupling (RFDR) (31)P solid-state NMR experiments were carried out on solid samples prepared in different conditions (i.e., temperature and atmosphere) and quenched at room temperature to identify frozen intermediate species in their metastable state. On the basis of this approach, we propose a model for the LaPO(4) formation based on a multistep mechanism which highlights the strong reactivity of ADP toward the alkaline salts but without final change in the composition of the solvent.

  10. 制备条件对La3+掺杂BiPO4光催化性能的影响%Effects of preparation process on photocatalytic activity of La3+doped BiPO4

    Institute of Scientific and Technical Information of China (English)

    全玉莲

    2016-01-01

    La3+-doped BiPO4 photocatalysts were fabricated via a hydrothermal process with different hydrothermal temperatures, time,and different solvents. The structures and morphologies of the samples were analyzed by XRD and SEM. The photocatalytic ac-tivities were evaluated by the degradation of methylene blue. It is found that reaction time and temperature,solvent content influence the structure,crystallinity and grain size of the products. The photocatalytic activities of the La3+-BiPO4 prepared at 200℃ and 3h is the best while the solvent is water,the degradation efficiency of methylene blue in 90 min reaches 95%under the UV light irradia-tion.%采用水热合成法在不同温度、时间、溶剂条件下制备了 La3+掺杂 BiPO4光催化剂,利用 X 射线衍射( XRD)、扫描电镜( SEM)技术对样品的结构和形貌进行了表征。以亚甲基蓝为目标污染物,探讨了不同条件合成的La3+-BiPO4的光催化性能。结果表明:水热温度和时间、溶剂对合成La3+-BiPO4的晶体结构、结晶度、晶粒尺寸等因素有较大的影响。在水热温度为200℃、时间为3h,溶剂为水的条件下制备的La3+-BiPO4对亚甲基蓝的降解效果最好,紫外光照90min后降解率达到95%。

  11. Public lighting.

    NARCIS (Netherlands)

    Schreuder, D.A.

    1986-01-01

    The function of public lighting and the relationship between public lighting and accidents are considered briefly as aspects of effective countermeasures. Research needs and recent developments in installation and operational described. Public lighting is an efficient accident countermeasure, but

  12. Apparatus and method for monitoring of gas having stable isotopes

    Science.gov (United States)

    Clegg, Samuel M; Fessenden-Rahn, Julianna E

    2013-03-05

    Gas having stable isotopes is monitored continuously by using a system that sends a modulated laser beam to the gas and collects and transmits the light not absorbed by the gas to a detector. Gas from geological storage, or from the atmosphere can be monitored continuously without collecting samples and transporting them to a lab.

  13. Molecular carbon isotopic evidence for the origin of geothermal hydrocarbons

    Science.gov (United States)

    Des Marais, D. J.; Donchin, J. H.; Nehring, N. L.; Truesdell, A. H.

    1981-01-01

    Isotopic measurements of individual geothermal hydrocarbons that are, as a group, of higher molecular weight than methane are reported. It is believed in light of this data that the principal source of hydrocarbons in four geothermal areas in western North America is the thermal decomposition of sedimentary or groundwater organic matter.

  14. Apparatus and method for monitoring of gas having stable isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Clegg, Samuel M; Fessenden-Rahn, Julianna E

    2013-03-05

    Gas having stable isotopes is monitored continuously by using a system that sends a modulated laser beam to the gas and collects and transmits the light not absorbed by the gas to a detector. Gas from geological storage, or from the atmosphere can be monitored continuously without collecting samples and transporting them to a lab.

  15. Prompt detection of alpha particles from 210Po: another clue to the origin of rock varnish?

    Science.gov (United States)

    Hodge, Vernon F; Farmer, Dennis E; Diaz, Tammy; Orndorff, Richard L

    2005-01-01

    Alpha particles have been measured coming from the surfaces of rocks covered with dark red-brown rock varnish, as well as rocks that appear to have little, if any, varnish. A pronounced peak at 5.3 MeV indicates the presence of 210Po, a short-lived natural-radioactive element. Surface activities for 33 samples range from 0.008 Bq/cm2 to 0.065 Bq/cm2. It is estimated that this nuclide is concentrated 10(11) times in these paper-thin coatings above its concentration in ground-level air. Gamma rays from the decay of 137Cs, a product of testing nuclear weapons some 50 years ago, were also detected. Analysis of samples of varnish stripped from the rock revealed traces of 239,240Pu and 238Pu. The presence of all of these isotopes strongly supports the theory that varnish films derive their building blocks from the atmosphere and, with time, all rocks in arid environments will become coated.

  16. An EXAFS study of the luminescent Bi3+ center in LaPO4---Bi

    NARCIS (Netherlands)

    Zon, F.B.M. van; Koningsberger, D.C.; Oomen, E.W.J.L.; Blasse, G.

    1987-01-01

    In order to determine the oxygen coordination of the Bi3+ ion in LaPO4---Bi, extended X-ray absorption fine structure (EXAFS) spectra were measured of BiPO4 and LaPO4---Bi. Analysis of the EXAFS data shows that the Bi3+ ion in LaPO4---Bi occupies the La3+ site, but that the oxygen coordination of th

  17. Significant visible-light photocatalytic enhancement in Rhodamine B degradation of silver orthophosphate via the hybridization of N-doped graphene and poly(3-hexylthiophene).

    Science.gov (United States)

    Zhang, Yanlin; Xie, Churu; Gu, Feng Long; Wu, Honghai; Guo, Qiang

    2016-09-05

    Organic pollutants as typical water contaminants are potentially harmful to human health. In this study, we suggested that the novel Ag3PO4/N-doped graphene (NG)/Poly(3-hexylthiophene) (P3HT) composites can remove the organic dye Rhodamine B (RhB) from water. This Ag3PO4-based photocatalyst was synthesized via a facile method and subsequently characterized by XRD, SEM, TEM, XPS, Raman spectroscopy, PL spectroscopy, and UV-vis DRS. The photocatalytic activity of Ag3PO4/NG/P3HT composites is significantly higher than that of pristine Ag3PO4, Ag3PO4/NG, and Ag3PO4/P3HT for RhB degradation under visible light irradiation, especially the kinetic constant of Ag3PO4/NG/P3HT is more than 6 times of pristine Ag3PO4. The reactive oxygen species trapping experiments indicate that the degradation of RhB over the Ag3PO4/NG/P3HT composites mainly results from the holes oxidation and superoxide radical reduction. Besides, Ag3PO4/NG/P3HT composites exhibit better recyclability and stability than pristine Ag3PO4. Furthermore, the photocatalytic mechanism of Ag3PO4/NG/P3HT composites for RhB degradation under visible light was proposed as the synergistic effect of irradiated Ag3PO4, P3HT and NG sheets on the effective separation of photogenerated electron-hole pairs, and the enhancement of visible light absorbance.

  18. Band structure engineering of anatase TiO2 by metal-assisted P-O coupling.

    Science.gov (United States)

    Wang, Jiajun; Meng, Qiangqiang; Huang, Jing; Li, Qunxiang; Yang, Jinlong

    2014-05-07

    In this work, we demonstrate that the metal-assisted P-O coupling is an effective approach to improve the photoelectrochemical properties of TiO2. The (Sc + P) and (In + P) codoping effects on electronic structures and photocatalytic activities of anatase TiO2 are examined by performing hybrid density functional theory calculations. It is found that the coupling of P dopant with the second-nearest neighboring O atom assisted by acceptor metals (Sc/In) leads to the fully occupied and delocalized intermediate bands within the band gap of anatase TiO2, which is driven by the P-O antibonding states (π*). This metal-assisted P-O coupling can prevent the recombination of photogenerated electron-hole pairs and effectively reduce the band gap of TiO2. Moreover, the band edge alignments in (Sc + P) and (In + P) codoped anatase TiO2 are desirable for water-splitting. The calculated optical absorption curves indicate that (Sc + P) and (In + P) codoping in anatase TiO2 can also effectively enhance the visible light absorption.

  19. Systematic study of photoluminescence, lyoluminescence and mechanoluminescence in Ce3+ - and Eu3+ -activated Li3 PO4 phosphors.

    Science.gov (United States)

    Sahu, A K; Kore, Bhushan P; Chowdhary, P S; Nayar, V; Dhoble, S J

    2014-02-01

    Li3 PO4 phosphor was prepared using a modified solid-state diffusion technique. In this work, photoluminescence, lyoluminescence and mechanoluminescence studies were carried out in a Li3 PO4 microcrystalline powder doped with different rare earths. In photoluminescence studies, characteristic emission of Ce and Eu was observed. The lyoluminescence glow curves of Li3 PO4 microcrystals show that lyoluminescence intensity initially increases with time and then decreases exponentially. The decay time consists of two components for all masses. The dependence of decay time, especially the longer component, on mass has been investigated. Experiments on γ-irradiated crystals have proved that the light emission originates from the recombination of released F-centres with trapped holes (V2-centres) at the sulfuric acid-solid interface. Incorporation of bivalent alkali in solid lithium phosphate leads to an enhancement of lyoluminescence. A possible explanation for the experimental results has been attempted. The phosphor has a mechanoluminescence single glow peak. Mechanoluminescence intensity under various loading conditions was investigated. It is observed that mechanoluminescence intensity increases with increasing impurity concentration and increasing piston impact velocity. The results may be considered as only being of academic interest in solid-state materials. Copyright © 2013 John Wiley & Sons, Ltd.

  20. Structure twinning, electronic and photoluminescence properties of yavapaiite-type orthophosphate BaTi(PO4)2

    Science.gov (United States)

    Zhao, Dan; Ma, Fa-Xue; Yang, Hong; Wei, Wei; Fan, Yun-Chang; Zhang, Lei; Xin, Xia

    2016-12-01

    A ternary orthophosphate BaTi(PO4)2 has been prepared using a high temperature molten salt method and structurally determined by single crystal X-Ray diffraction analysis. It crystallizes in yavapaiite-type structure with monoclinic space group C2/m. The structure was refined by a non-merohedral twinning model with the twin law (-0.435 1.4350 -0.564 -0.435 0 0.097 -0.099 1). Band structure calculation using the density functional theory (DFT) method indicates that BaTi(PO4)2 has a direct bond gap of about 3.00 eV, which is well fitted with the experimental value of 2.95 eV. The photoluminescence excitation and emission spectra, decay curve, and the color coordinates for BaTi(PO4)2 were investigated. It can be efficiently excited by UV light (270 nm) and presents blue-green emission (centered at 506 nm), which may be attributed to the lattice defect emission.

  1. Band structure engineering of anatase TiO{sub 2} by metal-assisted P-O coupling

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Jiajun; Meng, Qiangqiang [Hefei National Laboratory for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei, Anhui 230026 (China); Huang, Jing [Hefei National Laboratory for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei, Anhui 230026 (China); School of Materials and Chemical Engineering, Anhui Jianzhu University, Hefei, Anhui 230601 (China); Li, Qunxiang, E-mail: liqun@ustc.edu.cn; Yang, Jinlong [Hefei National Laboratory for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei, Anhui 230026 (China); Synergetic Innovation Center of Quantum Information and Quantum Physics, University of Science and Technology of China, Hefei, Anhui 230026 (China)

    2014-05-07

    In this work, we demonstrate that the metal-assisted P-O coupling is an effective approach to improve the photoelectrochemical properties of TiO{sub 2}. The (Sc + P) and (In + P) codoping effects on electronic structures and photocatalytic activities of anatase TiO{sub 2} are examined by performing hybrid density functional theory calculations. It is found that the coupling of P dopant with the second-nearest neighboring O atom assisted by acceptor metals (Sc/In) leads to the fully occupied and delocalized intermediate bands within the band gap of anatase TiO{sub 2}, which is driven by the P-O antibonding states (π*). This metal-assisted P-O coupling can prevent the recombination of photogenerated electron-hole pairs and effectively reduce the band gap of TiO{sub 2}. Moreover, the band edge alignments in (Sc + P) and (In + P) codoped anatase TiO{sub 2} are desirable for water-splitting. The calculated optical absorption curves indicate that (Sc + P) and (In + P) codoping in anatase TiO{sub 2} can also effectively enhance the visible light absorption.

  2. Stable Isotope Measurements of Carbon Dioxide, Methane, and Hydrogen Sulfide Gas Using Frequency Modulation Spectroscopy

    Science.gov (United States)

    Nowak-Lovato, K.

    2014-12-01

    Seepage from enhanced oil recovery, carbon storage, and natural gas sites can emit trace gases such as carbon dioxide, methane, and hydrogen sulfide. Trace gas emission at these locations demonstrate unique light stable isotope signatures that provide information to enable source identification of the material. Light stable isotope detection through surface monitoring, offers the ability to distinguish between trace gases emitted from sources such as, biological (fertilizers and wastes), mineral (coal or seams), or liquid organic systems (oil and gas reservoirs). To make light stable isotope measurements, we employ the ultra-sensitive technique, frequency modulation spectroscopy (FMS). FMS is an absorption technique with sensitivity enhancements approximately 100-1000x more than standard absorption spectroscopy with the advantage of providing stable isotope signature information. We have developed an integrated in situ (point source) system that measures carbon dioxide, methane and hydrogen sulfide with isotopic resolution and enhanced sensitivity. The in situ instrument involves the continuous collection of air and records the stable isotope ratio for the gas being detected. We have included in-line flask collection points to obtain gas samples for validation of isotopic concentrations using our in-house isotope ratio mass spectroscopy (IRMS). We present calibration curves for each species addressed above to demonstrate the sensitivity and accuracy of the system. We also show field deployment data demonstrating the capabilities of the system in making live dynamic measurements from an active source.

  3. Non-chondritic iron isotope ratios in planetary mantles as a result of core formation

    Science.gov (United States)

    Elardo, Stephen M.; Shahar, Anat

    2017-02-01

    Information about the materials and conditions involved in planetary formation and differentiation in the early Solar System is recorded in iron isotope ratios. Samples from Earth, the Moon, Mars and the asteroid Vesta reveal significant variations in iron isotope ratios, but the sources of these variations remain uncertain. Here we present experiments that demonstrate that under the conditions of planetary core formation expected for the Moon, Mars and Vesta, iron isotopes fractionate between metal and silicate due to the presence of nickel, and enrich the bodies' mantles in isotopically light iron. However, the effect of nickel diminishes at higher temperatures: under conditions expected for Earth's core formation, we infer little fractionation of iron isotopes. From our experimental results and existing conceptual models of magma ocean crystallization and mantle partial melting, we find that nickel-induced fractionation can explain iron isotope variability found in planetary samples without invoking nebular or accretionary processes. We suggest that near-chondritic iron isotope ratios of basalts from Mars and Vesta, as well as the most primitive lunar basalts, were achieved by melting of isotopically light mantles, whereas the heavy iron isotope ratios of terrestrial ocean floor basalts are the result of melting of near-chondritic Earth mantle.

  4. An Archean Terrestrial Fractionation Line for Oxygen Isotopes

    Science.gov (United States)

    Rumble, D.; Blake, R. E.; Bao, H.; Bowring, S.; Komiya, T.; Rosing, M.; Ueno, Y.

    2008-12-01

    The Terrestrial Fractionation Line (TFL) for oxygen isotopes is defined by 17O/16O and 18O/16O analyses of meteoric waters, seawater, sedimentary, metamorphic, and igneous rocks and constituent minerals. Interlaboratory measurements of the slope of the TFL on a plot of d18O vs. d17O revealed eclogitic garnets with a slope of 0.526 and hydrothermal quartz of 0.524 from rocks younger than 0.8 Ga (Giga years before present). New measurements show Archean metamorphic rocks and minerals from Barberton, (3.2 Ga, S. Africa), Isua (3.8 Ga, Greenland), and Acasta (4.0 Ga, Canada) have a slope of 0.524 +/- 0.002 (95% confidence, MSWD = 0.66). Analysis of Ag3PO4 prepared from apatite mineral separates from Isua meta-sediments gives a slope of 0.509 +/- 0.022 (95% confidence, MSWD = 0.59). Taken at face value, steeper slopes on a d17O vs. d18O diagram indicate an approach towards isotope exchange equilibrium. Lower slopes are expected when isotope fractionation is kinetically controlled. The lower slope of 0.509 for Isua apatite suggests that the formation of orthophosphate was kinetically controlled. Kinetic fractionations are known to occur during catalysis of reactions by enzymes secreted by microbes. Enzymatic catalysis confers an advantage on organisms because energy-producing reactions may be induced to occur at lower temperature conditions more accessible to the organism. May it be definitively concluded that enzymatic catalysis was responsible for the measured 0.509 slope? No, abiotic kinetic fractionation cannot be disproven with existing data. The preparation of Ag3PO4 from apatite may have introduced kinetic fractionation as an analytical artifact. Conclusions fully supported by the data suggest: (1) Mixing accompanying the violent birth of the Earth- Moon system had already succeeded in establishing Earth's current oxygen isotope composition by 4.0 Ga; and (2) No trace of an episode of late heavy meteorite bombardment remains in the oxygen isotope compositions of

  5. A Hybrid PO - Higher-Order Hierarchical MoM Formulation using Curvilinear Geometry Modeling

    DEFF Research Database (Denmark)

    Jørgensen, E.; Meincke, Peter; Breinbjerg, Olav

    2003-01-01

    A very efficient hybrid PO-MoM method has been presented. In contrast to existing methods, the present solution employs higher-order hierarchical basis functions to discretize the MoM and PO currents. This allows to reduce the number of basis functions in both the PO and MoM regions considerably...

  6. Water isotopes in desiccating lichens

    Science.gov (United States)

    Cuntz, Matthias; Máguas, Cristina; Lakatos, Michael

    2009-01-01

    The stable isotopic composition of water is routinely used as a tracer to study water exchange processes in vascular plants and ecosystems. To date, no study has focussed on isotope processes in non-vascular, poikilohydric organisms such as lichens and bryophytes. To understand basic isotope exchange processes of non-vascular plants, thallus water isotopic composition was studied in various green-algal lichens exposed to desiccation. The study indicates that lichens equilibrate with the isotopic composition of surrounding water vapour. A model was developed as a proof of concept that accounts for the specific water relations of these poikilohydric organisms. The approach incorporates first their variable thallus water potential and second a compartmentation of the thallus water into two isotopically distinct but connected water pools. Moreover, the results represent first steps towards the development of poikilohydric organisms as a recorder of ambient vapour isotopic composition. PMID:19888598

  7. Distinguishing phosphate from fertilizers and wastewater treatment plant effluents in Western Canada using oxygen isotope measurements

    Science.gov (United States)

    Fau, Veronique; Nightingale, Michael; Tamburini, Frederica; Mayer, Bernhard

    2014-05-01

    The successful application of oxygen isotope ratios as a tracer for phosphate in aquatic ecosystems requires that different sources of phosphate are isotopically distinct. The objective of this study was to determine whether the oxygen isotope ratios of phosphate from fertilizers and effluents from wastewater treatment plants in Western Canada are isotopically distinct. Therefore, we carried out oxygen isotope analyses on phosphate in effluent from five different wastewater treatment plants (WWTP) in the Bow River watershed of Alberta, Canada. Samples were collected directly from the final effluent (post-UV) in Banff and Canmore upstream of Calgary, and from effluents of Calgary's WWTPs at Bonnybrook, Fish Creek and Pine Creek. We also carried out oxygen isotope analyses on a variety of phosphate-containing fertilizers that are widely used in Western Canada. Historically, most of the phosphate contained in manufactured fertilizers sold in Alberta came from two distinct deposits: 1) a weathered Pliocene igneous carbonatite located in eastern Canada, and 2) the Permian Phosphoria Formation in the western USA. Phosphate (PO43-) contained in the water or the fertilizer was concentrated and quantitatively converted to pure silver phosphate (Ag3PO4). The silver phosphate was then reduced with carbon in an oxygen free environment using a TC/EA pyrolysis reactor linked to a mass spectrometer where 18O/16O ratios of CO were measured in continuous flow mode. Preparation of samples for δ18OPO4 analyses was conducted using the Magnesium Induced Coprecipitation (MAGIC) method. Expected oxygen isotope ratios for phosphate in equilibrium with water (δ18Oeq) were calculated using the Longinelli and Nuti equation: T (° C) = 111.4 - 4.3 (δ18Oeq - δ18Owater). Measured δ18O values of phosphate for fertilizer samples varied from 8 to 25 oÈ®n average, fertilizer samples of sedimentary origin had higher δ18O values (15.8) than those of igneous origin (11.5). Phosphate isotopic

  8. WOW: light print, light propel, light point

    DEFF Research Database (Denmark)

    Glückstad, Jesper; Bañas, Andrew Rafael; Aabo, Thomas

    2012-01-01

    anywhere in a sample at any orientation using real-time 3D optical micromanipulation with six degrees of freedom. One of the key aspects of our demonstrated WOWs is the change in direction of in-coupled light and the marked increase in numerical aperture of the out-coupled light. Hence, each light...... propelled WOW can tap from a relatively broad incident beam and generate a much more tightly confined light at its tip. The presentation contains both numerical simulations related to the propagation of light through a WOW and preliminary experimental demonstrations on our BioPhotonics Workstation...

  9. Downconversion and upconversion emissions of GdPO{sub 4}:Yb{sup 3+}/Tb{sup 3+} and its potential applications in solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Yimin [Changchun University of Science and Technology, Changchun, 130022 (China); Jilin Vocational College of Industry and Technology, Jilin, 132013 (China); Zhang, Hongbo [Changchun University of Science and Technology, Changchun, 130022 (China); Qu, Shanshan [Liaoning Police College, Dalian, 116036 (China); Su, Chunhui, E-mail: sch@cust.edu.cn [Changchun University of Science and Technology, Changchun, 130022 (China); Changchun Normal University, Changchun, 130032 (China)

    2016-08-25

    GdPO{sub 4}:Yb{sup 3+}/Tb{sup 3+} powders were synthesized by a solid state reaction. The XRD patterns indicated that the obtained GdPO{sub 4}:Yb{sup 3+}/Tb{sup 3+} powders have the monoclinic phase. Under the excitation of lights in the ultraviolet region, GdPO{sub 4}:Yb{sup 3+}/Tb{sup 3+} powders show dominate green emission in the visible light region and emission band peaking at 980 nm in the infrared region along with shoulders at 1001 nm and 1024 nm, which originate from the {sup 5}D{sub 4} → {sup 7}F{sub j} (j = 6, 5, 4 and 3) transitions of Tb{sup 3+} and {sup 2}D{sub 5/2} → {sup 2}F{sub 7/2} transitions of Yb{sup 3+} ions, respectively. Under the excitation of 980 nm, GdPO{sub 4}:Yb{sup 3+}/Tb{sup 3+} powders show dominate green emission in the visible light region, which is based on the cooperative energy transfer between two Yb{sup 3+} ions and one Tb{sup 3+} ion. The results present successful doping of rare earth ions in particles with both up and down conversion fluorescence properties that can be used as potential spectrum converter in solar cells. - Highlights: • Emission bands of GdPO{sub 4}:Yb{sup 3+}/Tb{sup 3+} in visible an IR regions under UV excitation. • Energy transfer from Gd{sup 3+} to Tb{sup 3+} and from Tb{sup 3+} to Yb{sup 3+} under UV excitation. • Emission bands of GdPO{sub 4}:Yb{sup 3+}/Tb{sup 3+} in visible region under IR excitation. • Cooperative energy transfer from two Yb{sup 3+} ions to one Tb{sup 3+} ion under IR excitation. • Potential application of GdPO{sub 4}:Yb{sup 3+}/Tb{sup 3+} as spectrum converter in solar cells.

  10. Synthesis and luminescence characteristics of Dy{sup 3+} doped KLa(PO{sub 3}){sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Chemingui, S.; Ferhi, M., E-mail: ferhi.mounir@gmail.com; Horchani-Naifer, K.; Férid, M.

    2015-10-15

    Polycrystalline powders of KLa{sub (1−x)}Dy{sub x}(PO{sub 3}){sub 4} (x=0.5%, 1%, 5% and 10%) with linear chain have been grown by solid state reaction. The obtained powders are characterized by X-ray powder diffraction, FTIR and Raman spectroscopies. Emission, excitation spectra and decay curves analysis have been used to study the spectroscopic properties of Dy{sup 3+} in KLa(PO{sub 3}){sub 4}. The photoluminescence spectra show two characteristic blue and yellow bands of Dy{sup 3+}. The yellow-to-blue emission intensity ratios and CIE chromaticity coordinates have been determined from emission spectra to evaluate the emitted light as function of Dy{sup 3+} concentration. The measured decay rates for {sup 4}F{sub 9/2}→{sup 6}H{sub 15/2} deviated from exponential to non-exponential shape with increase of Dy{sup 3+} concentration. The observed non-exponential behavior of the decay curve has been fitted to Inokuti–Hirayama model, which indicates that the energy transfer between the donor and the acceptor is of dipole–dipole nature. The energy transfer, between the donor (excited Dy{sup 3+}) and the acceptor (unexcited Dy{sup 3+}), increases with Dy{sup 3+} ions concentration. - Highlights: • Polycrystalline powders of KLa{sub (1−x)}Dy{sub x}(PO{sub 3}){sub 4} were grown by solid state reaction. • The obtained samples are characterized by XRD, FTIR and Raman spectroscopies. • The luminescent properties of Dy{sup 3+} in KLa(PO{sub 3}){sub 4} are investigated. • Lifetime and chromatic coordinates depend strongly on Dy{sup 3+} concentration. • White and blue emissions are obtained at high and low concentration, respectively.

  11. Bonding analysis using localized relativistic orbitals: water, the ultrarelativistic case and the heavy homologues H2X (X = Te, Po, eka-Po).

    Science.gov (United States)

    Dubillard, S; Rota, J-B; Saue, T; Faegri, K

    2006-04-21

    We report the implementation of Pipek-Mezey [J. Chem. Phys. 90, 4916 (1989)] localization of molecular orbitals in the framework of a four-component relativistic molecular electronic structure theory. We have used an exponential parametrization of orbital rotations which allows the use of unconstrained optimization techniques. We demonstrate the strong basis set dependence of the Pipek-Mezey localization criterion and how it can be eliminated. We have employed localization in conjunction with projection analysis to study the bonding in the water molecule and its heavy homologues. We demonstrate that in localized orbitals the repulsion between hydrogens in the water molecule is dominated by electrostatic rather than exchange interactions and that freezing the oxygen 2s orbital blocks polarization of this orbital rather than hybridization. We also point out that the bond angle of the water molecule cannot be rationalized from the potential energy alone due to the force term of the molecular virial theorem that comes into play at nonequilibrium geometries and which turns out to be crucial in order to correctly reproduce the minimum of the total energy surface. In order to rapidly assess the possible relativistic effects we have carried out the geometry optimizations of the water molecule at various reduced speed of light with and without spin-orbit interaction. At intermediate speeds, the bond angle is reduced to around 90 degrees , as is known experimentally for H(2)S and heavier homologues, although our model of ultrarelativistic water by construction does not allow any contribution from d orbitals to bonding. At low speeds of light the water molecule becomes linear which is in apparent agreement with the valence shell electron pair repulsion (VSEPR) model since the oxygen 2s12 and 2p12 orbitals both become chemically inert. However, we show that linearity is brought about by the relativistic stabilization of the (n + 1)s orbital, the same mechanism that leads to an

  12. PoInTree: A Polar and Interactive Phylogenetic Tree

    Institute of Scientific and Technical Information of China (English)

    Carreras Marco; Gianti Eleonora; Sartori Luca; Plyte Simon Edward; Isacchi Antonella; Bosotti Roberta

    2005-01-01

    PoInTree (Polar and Innteractive Tree) is an application that allows to build, visualize, and customize phylogenetic trees in a polar, interactive, and highly flexible view. It takes as input a FASTA file or multiple alignment formats. Phylogenetic tree calculation is based on a sequence distance method and utilizes the Neighbor Joining (NJ) algorithm. It also allows displaying precalculated trees of the major protein families based on Pfam classification. In PoInTree, nodes can be dynamically opened and closed and distances between genes are graphically represented.Tree root can be centered on a selected leaf. Text search mechanism, color-coding and labeling display are integrated. The visualizer can be connected to an Oracle database containing information on sequences and other biological data, helping to guide their interpretation within a given protein family across multiple species.The application is written in Borland Delphi and based on VCL Teechart Pro 6 graphical component (Steema software).

  13. Electric charge spectrum of recoiling {sup 218}Po

    Energy Technology Data Exchange (ETDEWEB)

    Abou-Khalil, R. [Institut de Radioprotection et de Surete Nucleaire (IRSN)/Service d' Etudes et de Recherches en Aerodispersion des polluants et en Confinement, B.P 68, 91192 Gif-sur-Yvette Cedex (France); Departement de Recherches Subatomiques, Institut Pluridisciplinaire Hubert-Curien, Groupe de Radioprotection et Mesures Environnementales (RaMsEs), Universite Louis Pasteur Strasbourg I, BP 28, 67037 Strasbourg Cedex 2 (France); Michielsen, N., E-mail: nathalie.michielsen@irsn.f [Institut de Radioprotection et de Surete Nucleaire (IRSN)/Service d' Etudes et de Recherches en Aerodispersion des polluants et en Confinement, B.P 68, 91192 Gif-sur-Yvette Cedex (France); Della-Negra, S. [Institut de Physique Nucleaire (IPN), F-91406 Orsay (France); Nourreddine, A.; Baussan, E. [Departement de Recherches Subatomiques, Institut Pluridisciplinaire Hubert-Curien, Groupe de Radioprotection et Mesures Environnementales (RaMsEs), Universite Louis Pasteur Strasbourg I, BP 28, 67037 Strasbourg Cedex 2 (France)

    2009-10-15

    The chemical and physical properties of a radioactive nanometric aerosol are important in determining its behaviour in indoor atmospheres and play a major part in determining its potential health effects. In a well defined experimental system, mass spectrometry coupled to the Time-of-Flight technique, we measured the electric charge of {sup 218}Po at the end of its recoil path. The charge distribution of the recoiling {sup 218}Po is mainly neutral and singly charged with a very small multicharged fraction. In case of radon progeny embedded in solid matter this one can play a major role in the surface ionisation processes versus electron and ion emission induced by the passage of the alpha recoils through the surface.

  14. počet potrubní trasy parovodu

    OpenAIRE

    Majer, Jan

    2016-01-01

    Práce objasňuje problematiku návrhového a kontrolního výpočtu parovodní potrubní trasy. K provedení analýzy jsou využity dva výpočtové programy – AutoPIPE a Ansys. V programu AutoPIPE je u potrubní trasy řešena problematika vhodného uložení a teplotní dilatace. Výsledky pevnostní analýzy z obou programů jsou vyhodnoceny dle normy ČSN EN 13480. This thesis describes issues related to design and structural analysis of steam pipeline. Analysis are done by using two different software program ...

  15. High pressure structural phase transitions of PbPo

    Energy Technology Data Exchange (ETDEWEB)

    Bencherif, Y.; Boukra, A. [Departement de Physique, Faculte des Sciences, Universite de Mostaganem (Algeria); Departement de Physique, Universite des Sciences et de la Technologie d' Oran, USTO, Oran (Algeria); Zaoui, A., E-mail: azaoui@polytech-lille.fr [Universite Lille Nord de France, LGCgE (EA 4515) Lille1, Polytech' Lille, Cite Scientifique, Avenue Paul Langevin, 59655 Villeneuve D' Ascq Cedex (France); Ferhat, M. [Departement de Physique, Universite des Sciences et de la Technologie d' Oran, USTO, Oran (Algeria)

    2012-09-01

    First-principles calculations have been performed to investigate the high pressure phase transitions and dynamical properties of the less known lead polonium compound. The calculated ground state parameters for the NaCl phase show good agreement with the experimental data. The obtained results show that the intermediate phase transition for this compound is the orthorhombic Pnma phase. The PbPo undergoes from the rocksalt to Pnma phase at 4.20 GPa. Further structural phase transition from intermediate to CsCl phase has been found at 8.5 GPa. In addition, phonon dispersion spectra were derived from linear-response to density functional theory. In particular, we show that the dynamical properties of PbPo exhibit some peculiar features compared to other III-V compounds. Finally, thermodynamics properties have been also addressed from quasiharmonic approximation.

  16. La trayectoria poética de Adolfo Alonso Ares

    Directory of Open Access Journals (Sweden)

    Armando López Castro

    2010-03-01

    Full Text Available Los poemas de Adolfo Ares revelan una voz de lo natural, una resonancia de un mismo ritmo cósmico que articula tosa su escritura. Desde el punto de vista lingüístico, se puede decir que la cercanía del poeta a la lengua hablada, sin la cual no hay renovación posible, le permite crear un lenguaje dinámico, en continua transformación, con el cual cada experiencia poética adquiere un sentido nuevo. Tal ha sido la función del arte desde los tiempos más antiguos: integrar al hombre en el ritmo del universo, que a su vez ha de animar a la obra poética en su conjunto.

  17. Baseline concentration of Polonium-210 ((210)Po) in tuna fish.

    Science.gov (United States)

    Khan, M Feroz; Wesley, S Godwin

    2016-06-15

    Several species of tuna fish were analyzed for (210)Po content in their edible muscle tissues. This study was carried out as a part of baseline data generation around a large nuclear power plant situated at Kudankulam, southeast coast of India. The concentration of (210)Po in the muscle tissue ranged from 40.9±5.2 to 92.5±7.9Bq/kg of fresh fish, and the highest activity was recorded for the tuna Euthynnus affinis and the lowest for Auxis thazard. The committed effective dose to the local residents was calculated to be 62.7-141.8μSvyear(-1). Copyright © 2016 Elsevier Ltd. All rights reserved.

  18. Iron isotope systematics in planetary reservoirs

    Science.gov (United States)

    Sossi, Paolo A.; Nebel, Oliver; Foden, John

    2016-10-01

    = 0.10 ± 0.01 ‰ (2SE) after correction to primary magmas, and can be produced from single stage melt extraction. Conversely, iron isotopes in arc basalts are more varied (- 0.2 partial melting. Their iron isotope compositions are significantly lighter, suggesting they form from mantle re-enriched in light Fe and/or more depleted than Depleted MORB Mantle (DMM). If arc sources are more oxidised, an agent other than iron is required. Magmatic differentiation drives enrichment in heavy isotopes by partial melting of crustal rocks, fluid exsolution and crystallisation. Iron isotope trajectories in evolving magmas depend on their initial fO2 and whether the system is closed or open to oxygen and/or mass exchange. Granite end-members carry signatures diagnostic of their tectonic setting, where reduced, anorogenic A-type granites (δ57 Fe = + 0.4 ‰) are heavier than more oxidised I-types (δ57 Fe = + 0.2 ‰).

  19. Configuration Interaction calculations of positron binding to Be(3Po)

    CERN Document Server

    Bromley, M W J

    2006-01-01

    The Configuration Interaction method is applied to investigate the possibility of positron binding to the metastable beryllium (1s^22s2p 3Po) state. The largest calculation obtained an estimated energy that was unstable by 0.00014 Hartree with respect to the Ps + Be^+(2s) lowest dissociation channel. It is likely that positron binding to parent states with non-zero angular momentum is inhibited by centrifugal barriers.

  20. Duas poéticas, dois olhares sobre o Barroco

    Directory of Open Access Journals (Sweden)

    Rogério Barbosa da Silva

    1998-12-01

    Full Text Available Resumo: Este ensaio pretende estudar relações existentes entre as poéticas de Affonso Ávila e Haroldo de Campos no contexto da poesia contemporânea, compreendendo o sentido que o Barroco adquiriu em suas produções criativas e críticas. Palavras-chave: experimentalismo, poesia concreta, Barroco, poesia crítica

  1. Lattice dynamics of LuPO{sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Nipko, J.C. [Argonne National Lab., IL (United States)]|[Colorado State Univ., Fort Collins, CO (United States); Loong, C.-K. [Argonne National Lab., IL (United States); Loewenhaupt, M. [Technische Univ. Dresden (Germany); Reichardt, W.; Braden, M. [Forschungszentrum Karlsruhe GmbH Technik und Umwelt (Germany); Boatner, L.A. [Oak Ridge National Lab., TN (United States)

    1996-06-01

    Lutetium orthophosphate is an important nonmagnetic host material for rare-earth-activated luminescence applications. We have measured the LuPO{sub 4} phonon density of states and dispersion curves along the [{xi}00],[{xi}{xi}0], and [00{xi}] symmetry directions by neutron spectroscopy using polycrystalline and single-crystal samples. A quantitative analysis of the neutron results was carried out using a lattice-dynamical shell model.

  2. Silver Orthophosphate Immobilized on Flaky Layered Double Hydroxides as the Visible-Light-Driven Photocatalysts

    Directory of Open Access Journals (Sweden)

    Xianlu Cui

    2012-01-01

    Full Text Available Flaky layered double hydroxide (FLDH was prepared by the reconstruction of its oxide in alkali solution. The composites with FLDH/Ag3PO4 mass ratios at 1.6 : 1 and 3 : 1 were fabricated by the coprecipitation method. The powders were characterized by X-ray diffraction, field-emission scanning electron microscopy, transmission electron microscope, and UV-vis diffuse reflectance spectroscopy. The results indicated that the well-distributed Ag3PO4 in a fine crystallite size was formed on the surface of FLDH. The photocatalytic activities of the Ag3PO4 immobilized on FLDH were significantly enhanced for the degradation of acid red G under visible light irradiation compared to bare Ag3PO4. The composite with the FLDH/Ag3PO4 mass ratio of 3 : 1 showed a higher photocatalytic efficiency.

  3. Folic acid-conjugated GdPO4:Tb3+@SiO2 Nanoprobe for folate receptor-targeted optical and magnetic resonance bi-modal imaging

    Science.gov (United States)

    Xu, Xianzhu; Zhang, Xiaoying; Wu, Yanli

    2016-11-01

    Both fluorescent and magnetic nanoprobes have great potential applications for diagnostics and therapy. In the present work, a folic acid-conjugated and silica-modified GdPO4:Tb3+ (GdPO4:Tb3+@SiO2-FA) dual nanoprobe was strategically designed and synthesized for the targeted dual-modality optical and magnetic resonance (MR) imaging via a facile aqueous method. Their structural, optical, and magnetic properties were determined using transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR), ultraviolet-visible spectra (UV-Vis), photoluminescence (PL), and superconducting quantum interference device (SQUID). These results indicated that GdPO4:Tb3+@SiO2-FA were uniform monodisperse core-shell structured nanorods (NRs) with an average length of 200 nm and an average width of 25 nm. The paramagnetic property of the synthesized GdPO4:Tb3+@SiO2-FA NRs was confirmed with its linear hysteresis plot (M-H). In addition, the NRs displayed an obvious T1-weighted effect and thus it could potentially serve as a T1-positive contrast agent. The NRs emitted green lights due to the 5D4 → 7F5 transition of the Tb3+. The in vitro assays with NCI-H460 lung cancer cells and human embryonic kidney cell line 293T cells indicated that the GdPO4:Tb3+@SiO2-FA nanoprobe could specifically bind the cells bearing folate receptors (FR). The MTT assay of the NRs revealed that its cytotoxicity was very low. Further in vivo MRI experiments distinctively depict enhanced anatomical features in a xenograft tumor. These results suggest that the GdPO4:Tb3+@SiO2-FA NPs have excellent imaging and cell-targeting abilities for the folate receptor-targeted dual-modality optical and MR imaging and can be potentially used as the nanoprobe for bioimaging.

  4. A biokinetic study of {sup 209}Po in man

    Energy Technology Data Exchange (ETDEWEB)

    Henricsson, C.F.; Ranebo, Y. [Department of Medical Radiation Physics, Clinical Sciences in Lund, Lund University, Skane University Hospital in Lund (Sweden); Hansson, M. [Medical Radiation Physics, Department of Clinical Sciences in Malmoe, Lund University, Skane University Hospital in Malmoe (Sweden); Raeaef, C.L., E-mail: Christopher.Raaf@med.lu.se [Medical Radiation Physics, Department of Clinical Sciences in Malmoe, Lund University, Skane University Hospital in Malmoe (Sweden); Holm, E. [Norwegian Radiation Protection Authority, Osteras (Norway)

    2012-10-15

    Five adult volunteers participated in a biokinetic study of radioactive polonium. Portions of about 10 Bq of {sup 209}Po were orally administrated to four of the volunteers in a single ingestion. The fifth volunteer ingested a daily amount of 53 mBq of 209Po for 243 d to study the time to achieve equilibrium between intake and excretion for protracted intakes. For the subjects ingesting single intakes of {sup 209}Po complete sampling of urine and feces was subsequently collected the first few days upon the ingestion. The samples were processed with radiochemical extraction and analyzed with alpha spectrometry. In the study, the maximum daily excretion rates in feces were 18-50% of the ingested activity, observed within 3 d after intake. Regarding the urine excretion, the daily excretion peaked, on average, at 0.15-1% of the ingested activity within two days upon intake. These results indicate an average gastro-intestinal uptake fraction of 0.46 {+-} 0.08, which agrees well with earlier biokinetic studies of polonium in man. -- Highlights: Black-Right-Pointing-Pointer Human metabolism of an oral intake of polonium. Black-Right-Pointing-Pointer 4 individuals were administrated about 10 Bq polonium-209. Black-Right-Pointing-Pointer Gastro-intestinal uptake fraction, if orally administrated polonium-209 was investigated. Black-Right-Pointing-Pointer The biological half-time of polonium in human body was studied.

  5. Can Vanadium Be Substituted into LiFePO4

    Energy Technology Data Exchange (ETDEWEB)

    Omenya F.; Nam K.; Chernova N.A.; Upreti S.; Zavalij P.Y.; Nam K.-W.; Yang X.-Q.; Whittingham M.S.

    2011-11-08

    Vanadium is shown to substitute for iron in the olivine LiFePO{sub 4} up to at least 10 mol %, when the synthesis is carried out at 550 C. In the solid solution LiFe{sub 1-3y/2}V{sub y}PO{sub 4}, the a and b lattice parameters and cell volume decrease with increasing vanadium content, while the c lattice parameter increases slightly. However, when the synthesis is performed at 650 C, a NASICON phase, Li{sub 3}V{sub 2}(PO{sub 4}){sub 3}, is also formed, showing that solid solution is a function of the synthesis temperature. X-ray absorption near-edge structure indicates vanadium is in the 3+ oxidation state and in an octahedral environment. Magnetic studies reveal a shift of the antiferromagnetic ordering transition toward lower temperatures with increasing vanadium substitution, confirming solid solution formation. The addition of vanadium enhances the electrochemical performance of the materials especially at high current densities.

  6. Novel yellow-emitting Sr8MgLn(PO4)7:Eu2+ (Ln=Y, La) phosphors for applications in white LEDs with excellent color rendering index.

    Science.gov (United States)

    Huang, Chien-Hao; Chen, Teng-Ming

    2011-06-20

    Eu(2+)-activated Sr(8)MgY(PO(4))(7) and Sr(8)MgLa(PO(4))(7) yellow-emitting phosphors were successfully synthesized by solid-state reactions for applications in excellent color rendering index white light-emitting diodes (LEDs). The excitation and reflectance spectra of these phosphors show broad band excitation and absorption in the 250-450 nm near-ultraviolet region, which is ascribed to the 4f(7) → 4f(6)5d(1) transitions of Eu(2+). Therefore, these phosphors meet the application requirements for near-UV LED chips. Upon excitation at 400 nm, the Sr(8)MgY(PO(4))(7):Eu(2+) and Sr(8)MgLa(PO(4))(7):Eu(2+) phosphors exhibit strong yellow emissions centered at 518, 610, and 611 nm with better thermal stability than (Ba,Sr)(2)SiO(4) (570 nm) commodity phosphors. The composition-optimized concentrations of Eu(2+) in Sr(8)MgLa(PO(4))(7):Eu(2+) and Sr(8)MgY(PO(4))(7):Eu(2+) phosphors were determined to be 0.01 and 0.03 mol, respectively. A warm white-light near-UV LED was fabricated using a near-UV 400 nm chip pumped by a phosphor blend of blue-emitting BaMgAl(10)O(17):Eu(2+) and yellow-emitting Sr(8)MgY(PO(4))(7):0.01Eu(2+) or Sr(8)MgLa(PO(4))(7):0.03Eu(2+), driven by a 350 mA current. The Sr(8)MgY(PO(4))(7):0.01Eu(2+) and Sr(8)MgLa(PO(4))(7):0.03Eu(2+) containing LEDs produced a white light with Commission International de I'Eclairage (CIE) chromaticity coordinates of (0.348, 0.357) and (0.365, 0.328), warm correlated color temperatures of 4705 and 4100 K, and excellent color rendering indices of 95.375 and 91.75, respectively.

  7. Improved photoelectrochemical performance of Z-scheme g-C{sub 3}N{sub 4}/Bi{sub 2}O{sub 3}/BiPO{sub 4} heterostructure and degradation property

    Energy Technology Data Exchange (ETDEWEB)

    Li, Junqi, E-mail: sfmlab@163.com; Yuan, Huan; Zhu, Zhenfeng

    2016-11-01

    Highlights: • A novel Z-scheme g-C{sub 3}N{sub 4}/Bi{sub 2}O{sub 3}/BiPO{sub 4} composite was synthesized. • The Z-scheme system we made can remain the strong reducibility and oxidizability of the photocatalysts. • The solar light was made the utmost use both the ultraviolet and visible region light through the g-C{sub 3}N{sub 4}/Bi{sub 2}O{sub 3}/BiPO{sub 4} composite. - Abstract: In g-C{sub 3}N{sub 4}/Bi{sub 2}O{sub 3}/BiPO{sub 4}, the p–n junction between p-type Bi{sub 2}O{sub 3} and n-type BiPO{sub 4} was encapsulated by g-C{sub 3}N{sub 4} and a direct Z-scheme was built between g-C{sub 3}N{sub 4} and Bi{sub 2}O{sub 3}. The optical, morphological and photoelectrochemical (PEC) properties of BiPO{sub 4}, g-C{sub 3}N{sub 4}/BiPO{sub 4}, Bi{sub 2}O{sub 3}/BiPO{sub 4} and g-C{sub 3}N{sub 4}/Bi{sub 2}O{sub 3}/BiPO{sub 4} hierarchical Z-scheme system were studied. More than 90% photodegradation of methyl orange (MO) with the exposure of simulated solar light was achieved within 160 min with the g-C{sub 3}N{sub 4}/Bi{sub 2}O{sub 3}/BiPO{sub 4}, which displayed remarkably promoted photocatalytic activities than other samples. The electrochemical impedance spectra and photocurrent results also proved that efficient charge separation and better electron transport properties were achieved by g-C{sub 3}N{sub 4}/Bi{sub 2}O{sub 3}/BiPO{sub 4}. In general, the addition of g-C{sub 3}N{sub 4} can guide the residual electrons on p-type Bi{sub 2}O{sub 3} to recombine with photoholes of g-C{sub 3}N{sub 4} and make sure the left carries exhibit stronger oxidation and reduction ability to boost the production of active groups.

  8. Significant visible-light photocatalytic enhancement in Rhodamine B degradation of silver orthophosphate via the hybridization of N-doped graphene and poly(3-hexylthiophene)

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Yanlin, E-mail: zhangyl@scnu.edu.cn; Xie, Churu; Gu, Feng Long, E-mail: Gu@scnu.edu.cn; Wu, Honghai; Guo, Qiang

    2016-09-05

    Highlights: • The Ag{sub 3}PO{sub 4}/NG/P3HT composites were synthesized via a facile method. • The Ag{sub 3}PO{sub 4}/NG/P3HT composites exhibit excellent photocatalytic activity for RhB degradation. • The kinetic constant of Ag{sub 3}PO{sub 4}/NG/P3HT is more than 6 times of pristine Ag{sub 3}PO{sub 4}. • The composites show better recyclability and stability than pristine Ag{sub 3}PO{sub 4}. - Abstract: Organic pollutants as typical water contaminants are potentially harmful to human health. In this study, we suggested that the novel Ag{sub 3}PO{sub 4}/N-doped graphene (NG)/Poly(3-hexylthiophene) (P3HT) composites can remove the organic dye Rhodamine B (RhB) from water. This Ag{sub 3}PO{sub 4}-based photocatalyst was synthesized via a facile method and subsequently characterized by XRD, SEM, TEM, XPS, Raman spectroscopy, PL spectroscopy, and UV–vis DRS. The photocatalytic activity of Ag{sub 3}PO{sub 4}/NG/P3HT composites is significantly higher than that of pristine Ag{sub 3}PO{sub 4}, Ag{sub 3}PO{sub 4}/NG, and Ag{sub 3}PO{sub 4}/P3HT for RhB degradation under visible light irradiation, especially the kinetic constant of Ag{sub 3}PO{sub 4}/NG/P3HT is more than 6 times of pristine Ag{sub 3}PO{sub 4}. The reactive oxygen species trapping experiments indicate that the degradation of RhB over the Ag{sub 3}PO{sub 4}/NG/P3HT composites mainly results from the holes oxidation and superoxide radical reduction. Besides, Ag{sub 3}PO{sub 4}/NG/P3HT composites exhibit better recyclability and stability than pristine Ag{sub 3}PO{sub 4}. Furthermore, the photocatalytic mechanism of Ag{sub 3}PO{sub 4}/NG/P3HT composites for RhB degradation under visible light was proposed as the synergistic effect of irradiated Ag{sub 3}PO{sub 4}, P3HT and NG sheets on the effective separation of photogenerated electron-hole pairs, and the enhancement of visible light absorbance.

  9. Chromium isotope variations

    DEFF Research Database (Denmark)

    D'Arcy, Joan Mary

    is incorporated into carbonates. Hence, ancient carbonates can potentially record the Cr isotopic composition (δ53Cr ‰) of seawater in the geological past. Reliable application and interpretation of this proxy requires a detailed knowledge about processes that fractionate Cr on the Earth’s surface...... deposited during the Early Ordovician — a time of known redox instability in ancient oceans – exhibit a significant positive Cr isotope excursion of +0.5‰. This excursion is interpreted as the reductive drawn down of dissolved Cr in seawater in response to the development of a proximal anoxic sink...... of ancient marine sediments can be a useful tool for understanding the cycling of redox sensitive elements on a local scale....

  10. Isotopic and noble gas geochemistry in geothermal research

    Energy Technology Data Exchange (ETDEWEB)

    Kennedy, B.M.; DePaolo, D.J. [Lawrence Berkeley National Lab., CA (United States)

    1997-12-31

    The objective of this program is to provide, through isotopic analyses of fluids, fluid inclusions, and rocks and minerals coupled with improved methods for geochemical data analysis, needed information regarding sources of geothermal heat and fluids, the spatial distribution of fluid types, subsurface flow, water-rock reaction paths and rates, and the temporal evolution of geothermal systems. Isotopic studies of geothermal fluids have previously been limited to the light stable isotopes of H, C, and O. However, other isotopic systems such as the noble gases (He, Ne, Ar, Kr and Xe) and reactive elements (e.g. B, N, S, Sr and Pb) are complementary and may even be more important in some geothermal systems. The chemistry and isotopic composition of a fluid moving through the crust will change in space and time in response to varying chemical and physical parameters or by mixing with additional fluids. The chemically inert noble gases often see through these variations, making them excellent tracers for heat and fluid sources. Whereas, the isotopic compositions of reactive elements are useful tools in characterizing water-rock interaction and modeling the movement of fluids through a geothermal reservoir.

  11. GEOCHRONOMETRY & ISOTOPE GEOLOGY

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    <正>20050934 Chen Zhihong (Chinese Academy of Geological Sciences, Beijing 100037, China); Lu Songnian Age of the Fushui Intermediate-Mafic Intrusive Complex in the Qinling Orogen, New Zircon U - Pb and Whole -Rock Sm and Nd Isotope Chronological Evidence (Geological Bulletin of China, ISSN 1671-2552, CN11-4648/P, 23(4), 2004, p. 322-328, 3 illus. , 3 tables, 10 refs. )

  12. GEOCHRONOMETRY &ISOTOPE GEOLOGY

    Institute of Scientific and Technical Information of China (English)

    2013-01-01

    <正>20131727 Huang Xiaowen(State Key Laboratory of Ore Deposit Geochemistry,Institute of Geochemistry,Chinese Academy of Sciences,Guiyang 550002,China);Qi Liang Preliminary Study on Sample-Preparation for Re-Os Isotopic Dating of Pyrite(Geochimica,ISSN0379-1726,CN44-1398/P,41(4),2012,p.380-386,3illus.,2tables,25refs)Key words:pyrite,Re-Os dating

  13. GEOCHRONOMETRY & ISOTOPE GEOLOGY

    Institute of Scientific and Technical Information of China (English)

    2013-01-01

    <正>20132601 Cui Yurong(Tianjin Institute of Geology and Mineral Resources,China Geological Survey,Tianjin 300170,China);Zhou Hongying In Situ LA-MC-ICP-MS U-Pb Isotopic Dating of Monazite(Acta Geoscientica Sinica,ISSN0375-5444,CN11-1856/P,33(6),2012,p.865-876,6illus.,4tables,41refs.)Key words:monazite,U-Pb dating

  14. New hybridization of PO, SBR, and MoM for scattering by large complex conducting objects

    Institute of Scientific and Technical Information of China (English)

    Dong Chunzhu; Geng Fangzhi; Yin Hongcheng; Wang Chao

    2007-01-01

    As a marked extension of the traditional MoM-PO (method of moment-physical optics) hybrid method,a new hybridization of PO, SBR, and MoM (MoM-SBR/PO) is presented to calculate the multi-reflection contribution in the PO region efficiently by introducing the method of SBR based on RDN notion, which avoids the time-consuming iterative procedure and the choice of proper Green's function. As compared with the traditional MoM-PO hybrid method, the calculation efficiency of the proposed method is greatly improved, and its validity is verified by numerical results.

  15. Towards a construction grammar account of the distributive PO in Polish

    Directory of Open Access Journals (Sweden)

    Adam Przepiórkowski

    2015-11-01

    Full Text Available Towards a construction grammar account of the distributive PO in Polish Polish distributive constructions involving the form po are well known for their syntactic and semantic idiosyncrasy. The aim of this paper is to show that, contrary to the received wisdom, two different lexemes po take part in such constructions: a preposition and an adnumeral operator. This explains some of the idiosyncratic behaviour, namely, the apparent ability of po to combine with different grammatical cases. A preliminary Construction Grammar analysis is proposed which eschews the potential problem of missed generalisations that such a dual account of po might engender.

  16. Effect of Li3PO4 coating of layered lithium-rich oxide on electrochemical performance

    Science.gov (United States)

    Chen, Dongrui; Zheng, Feng; Li, Liu; Chen, Min; Zhong, Xiaoxin; Li, Weishan; Lu, Li

    2017-02-01

    A novel composite of layered lithium-rich oxide, Li-Rich@Li3PO4, coated with Li3PO4 is synthesized through polydopamine template method. Physical characterizations reveal that Li-Rich@Li3PO4 is composed of nanoparticles of 100-200 nm that are coated with a uniform Li3PO4 layer of about 5 nm in thickness. Galvanostatic charge/discharge tests demonstrate enhanced cycling stability and largely increased rate capability of the material after Li3PO4 coating.

  17. ISOTOPE METHODS IN HOMOGENEOUS CATALYSIS.

    Energy Technology Data Exchange (ETDEWEB)

    BULLOCK,R.M.; BENDER,B.R.

    2000-12-01

    The use of isotope labels has had a fundamentally important role in the determination of mechanisms of homogeneously catalyzed reactions. Mechanistic data is valuable since it can assist in the design and rational improvement of homogeneous catalysts. There are several ways to use isotopes in mechanistic chemistry. Isotopes can be introduced into controlled experiments and followed where they go or don't go; in this way, Libby, Calvin, Taube and others used isotopes to elucidate mechanistic pathways for very different, yet important chemistries. Another important isotope method is the study of kinetic isotope effects (KIEs) and equilibrium isotope effect (EIEs). Here the mere observation of where a label winds up is no longer enough - what matters is how much slower (or faster) a labeled molecule reacts than the unlabeled material. The most careti studies essentially involve the measurement of isotope fractionation between a reference ground state and the transition state. Thus kinetic isotope effects provide unique data unavailable from other methods, since information about the transition state of a reaction is obtained. Because getting an experimental glimpse of transition states is really tantamount to understanding catalysis, kinetic isotope effects are very powerful.

  18. Bayesian Integration of Isotope Ratios for Geographic Sourcing of Castor Beans

    Energy Technology Data Exchange (ETDEWEB)

    Webb-Robertson, Bobbie-Jo M.; Kreuzer, Helen W.; Hart, Garret L.; Ehleringer, James; West, Jason B.; Gill, Gary A.; Duckworth, Douglas C.

    2012-08-15

    Recent years have seen an increase in the forensic interest associated with the poison ricin, which is extracted from the seeds of the Ricinus communis plant. Both light element (C, N, O, and H) and strontium (Sr) isotope ratios have previously been used to associate organic material with geographic regions of origin. We present a Bayesian integration methodology that can more accurately predict the region of origin for a castor bean than individual models developed independently for light element stable isotopes or Sr isotope ratios. Our results demonstrate a clear improvement in the ability to correctly classify regions based on the integrated model with a class accuracy of 6 0 . 9 {+-} 2 . 1 % versus 5 5 . 9 {+-} 2 . 1 % and 4 0 . 2 {+-} 1 . 8 % for the light element and strontium (Sr) isotope ratios, respectively. In addition, we show graphically the strengths and weaknesses of each dataset in respect to class prediction and how the integration of these datasets strengthens the overall model.

  19. Stable isotope analysis of migratory connectivity in a threatened intra-African migrant, the Blue Swallow (Hirundo atrocaerulea)

    CSIR Research Space (South Africa)

    Wakelin, J

    2010-07-01

    Full Text Available isotope analysis of migratory connectivity in a threatened intra-African migrant, the Blue Swallow (Hirundo atrocaerulea) James Wakelin • Andrew E. McKechnie • Stephan Woodborne Received: 24 September 2009 / Revised: 28 April 2010 / Accepted: 2 July...), and the challenges inherent in conserving migrants are exacerbated when connections between populations are not well understood. Communicated by F. Bairlein. James Wakelin: Deceased. J. Wakelin Scientific Services, Ezemvelo KZN Wildlife, P.O. Box 13053...

  20. Evaluating the use of amber in palaeoatmospheric reconstructions: The carbon-isotope variability of modern and Cretaceous conifer resins

    Science.gov (United States)

    Dal Corso, Jacopo; Schmidt, Alexander R.; Seyfullah, Leyla J.; Preto, Nereo; Ragazzi, Eugenio; Jenkyns, Hugh C.; Delclòs, Xavier; Néraudeau, Didier; Roghi, Guido

    2017-02-01

    Stable carbon-isotope geochemistry of fossilized tree resin (amber) potentially could be a very useful tool to infer the composition of past atmospheres. To test the reliability of amber as a proxy for the atmosphere, we studied the variability of modern resin δ13C at both local and global scales. An amber δ13C curve was then built for the Cretaceous, a period of abundant resin production, and interpreted in light of data from modern resins. Our data show that hardening changes the pristine δ13C value by causing a 13C-depletion in solid resin when compared to fresh liquid-viscous resin, probably due to the loss of 13C-enriched volatiles. Modern resin δ13C values vary as a function of physiological and environmental parameters in ways that are similar to those described for leaves and wood. Resin δ13C varies between plant species and localities, within the same tree and between different plant tissues by up to 6‰, and in general increases with increasing altitudes of the plant-growing site. We show that, as is the case with modern resin, Cretaceous amber δ13C has a high variability, generally higher than that of other fossil material. Despite the high natural variability, amber shows a negative 2.5-3‰ δ13C trend from the middle Early Cretaceous to the Maastrichtian that parallels published terrestrial δ13C records. This trend mirrors changes in the atmospheric δ13C calculated from the δ13C and δ18O of benthic foraminiferal tests, although the magnitude of the shift is larger in plant material than in the atmosphere. Increasing mean annual precipitation and pO2 could have enhanced plant carbon-isotope fractionation during the Late Cretaceous, whereas changing pCO2 levels seem to have had no effect on plant carbon-isotope fractionation. The results of this study suggest that amber is a powerful fossil plant material for palaeoenvironmental and palaeoclimatic reconstructions. Improvement of the resolution of the existing data coupled with more detailed