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Sample records for group v elements

  1. Stable single-layer structure of group-V elements

    NASA Astrophysics Data System (ADS)

    Ersan, F.; Aktürk, E.; Ciraci, S.

    2016-12-01

    In addition to stable single-layer buckled honeycomb and washboard structures of group-V elements (or pnictogens P, As, Sb, and Bi) we show that these elements can also form two-dimensional, single-layer structures consisting of buckled square and octagon rings. An extensive analysis comprising the calculation of mechanical properties, vibration frequencies, and finite-temperature ab initio molecular dynamics confirms that these structures are dynamically and thermally stable and suitable for applications at room temperature and above. All these structures are semiconductors with a fundamental band gap, which is wide for P but decreases with increasing row number. The effect of the spin-orbit coupling decreases the band gap and is found to be crucial for Sb and Bi. These results are obtained from first-principles calculations based on density functional theory.

  2. A new structure of two-dimensional allotropes of group V elements

    PubMed Central

    Li, Ping; Luo, Weidong

    2016-01-01

    The elemental two-dimensional (2D) materials such as graphene, silicene, germanene, and black phosphorus have attracted considerable attention due to their fascinating physical properties. Structurally they possess the honeycomb or distorted honeycomb lattices, which are composed of six-atom rings. Here we find a new structure of 2D allotropes of group V elements composed of eight-atom rings, which we name as the octagonal tiling (OT) structure. First-principles calculations indicate that these allotropes are dynamically stable and are also thermally stable at temperatures up to 600 K. These allotropes are semiconductors with band gaps ranging from 0.3 to 2.0 eV, thus they are potentially useful in near- and mid-infrared optoelectronic devices. OT-Bi is also a 2D topological insulator (TI) with a band gap of 0.33 eV, which is the largest among the reported elemental 2D TIs, and this gap can be increased further by applying compressive strains. PMID:27150010

  3. Influence of Group IV and V Alloying Elements on the Microstructure Engineering and Deformation Behavior in Tantalum Carbides

    DTIC Science & Technology

    2015-04-06

    stable for a range of stoichiometry allowing a large amount of carbon loss. For the group VB compounds, the FCC structure of the metal atoms is...AFRL-OSR-VA-TR-2015-0092 Influence of Group IV and V Alloying Elements on the Microstructure Engineering GREGORY THOMPSON UNIVERSITY OF ALABAMA Final...31/03/2015 4. TITLE AND SUBTITLE Influence of Group IV and V Alloying Elements on the Microstructure Engineering and Deformation Behavior in

  4. Theoretical and Materials Chemistry of Some Group III and V Elements

    NASA Astrophysics Data System (ADS)

    Glass, John Arthur, Jr.

    The theoretical and material aspects of some group III and V compounds have been investigated. Phosphaborane clusters were investigated by modified neglect of differential overlap semi-empirical molecular orbital calculations (MNDO -SCF) to better understand important structural, electronic, and thermodynamic properties of these experimentally difficult species. The structural, thermodynamic and electronic properties of 111 phosphapentaborane cluster compounds have been calculated via MNDO-SCF. The geometry-optimized, minimum energy structures for all of the known and structurally characterized phosphaborane systems have been calculated. In each case, exceptionally good agreement was observed between the experimentally determined and the calculated structural parameters. Calculations for five classes of phosphapentaborane clusters have been completed and have been related to experimentally proposed structural types. Predictions concerning structural and chemical reactivities for unknown and known phosphapentaborane compounds have been made based on these MO calculations. Production of important thin film materials was discussed relative to chemical vapor deposition (CVD). Advantages of CVD over older thermodynamic deposition techniques were described. The CVD process has been briefly reviewed through seven primary steps. The importance of new source materials which meet stringent industrial requirements have been detailed relative to environmental, occupational safety, and contaminations considerations. Thin films of pure aluminum, aluminum boride and aluminum oxide have been prepared from the chemical vapor deposition (CVD) of rm Al(BH_4)_3, and rm AlH_2(BH_4) cdot N(CH_3)_3, on both single crystals and thermally sensitive substrates. Films were characterized by EDX, AES, SEM, XRD, and resistivity measurements and ranged in thickness from 500 A to 2 mu m. Each type of film was shown by AES to be compositionally uniform in the bulk sample with only very shallow

  5. Electrical activity, mode of incorporation and distribution coefficient of group V elements in Hg1-xCdxTe grown from tellurium rich liquid phase epitxial growth solutions

    NASA Astrophysics Data System (ADS)

    Vydyanath, H. R.; Ellsworth, J. A.; Devaney, C. M.

    1987-01-01

    Hg1-xCdxTe films were grown liquid phase epitaxially from tellurium rich solutions containing up to 10 at. % of the group V elements P, As, Sb, and Bi. Chemical analysis of the Te growth solutions and the films was carried out in conjunction with extensive Hall effect measurements on the films subsequent to various annealing treatments under Hg rich and Te rich conditions. Despite the presence of a large concentration of the group V elements in the Te source solution, the maximum concentration of these elements incorporated into the liquid phase epitaxially grown Hg1-xCdxTe appears to vary from <1015cm-3 for Bi up to 1017cm-3 for phosphorus and As implying a distribution coefficient varying from <10-5 for Bi up to 10-3 for P at growth temperature of ˜500° C. This low value of the distribution coefficient for group V elements for growths from Te rich solutions contrasts with the moderately high values reported in the literature to date for growth from Hg rich solutions as well as pseudobinary solutions (Bridgman growth). The widely differing distribution coefficients and hence the solubility of the group V elements for Hg rich and Te rich liquid phase epitaxial solutions is explained on the basis that the activity coefficient of the group V elements in Te rich solutions is probably orders of magnitude lower than it is in Hg rich solutions. Finally, the results of the anneals at 200° C under Hg saturated conditions with and without a 500° C Hg saturated preanneal have indicated n to p conversion in many of the films attesting to the amphoteric behavior of the group V elements in LPE grown Hg1-xCdxTe(s) similar to the previously reported behavior of P in bulk grown Hg0.8Cd0.2Te.

  6. Platinum-group element geochemistry of the Zhuqing Fe-Ti-V oxide ore-bearing mafic intrusions in western Yangtze Block, SW China: control of platinum-group elements by magnetite

    NASA Astrophysics Data System (ADS)

    Fan, Hong-Peng; Zhu, Wei-Guang; Zhong, Hong; Bai, Zhong-Jie; He, De-Feng; Ye, Xian-Tao; Chen, Cai-Jie; Cao, Chong-Yong

    2014-06-01

    Platinum-group element (PGE) geochemistry combined with elemental geochemistry and magnetite compositions are reported for the Mesoproterozoic Zhuqing Fe-Ti-V oxide ore-bearing mafic intrusions in the western Yangtze Block, SW China. All the Zhuqing gabbros display extremely low concentrations of chalcophile elements and PGEs. The oxide-rich gabbros contain relatively higher contents of Cr, Ni, Ir, Ru, Rh, and lower contents of Pt and Pd than the oxide-poor gabbros. The abundances of whole-rock concentrations of Ni, Ir, Ru, and Rh correlate well with V contents in the Zhuqing gabbros, implying that the distributions of these elements are controlled by magnetite. The fractionation between Ir-Ru-Rh and Pt-Pd in the Zhuqing gabbros is mainly attributed to fractional crystallization of chromite and magnetite, whereas Ru anomalies are mainly due to variable degrees of compatibility of PGE in magnetite. The order of relative incompatibility of PGEs is calculated to be Pd < Pt < Rh < Ir < Ru. The very low PGE contents and Cu/Zr ratios and high Cu/Pd ratios suggest initially S-saturated magma parents that were highly depleted in PGE, which mainly formed due to low degrees of partial melting leaving sulfides concentrating PGEs behind in the mantle. Moreover, the low MgO, Ni, Ir and Ru contents and high Cu/Ni and Pd/Ir ratios for the gabbros suggest a highly evolved parental magma. Fe-Ti oxides fractionally crystallized from the highly evolved magma and subsequently settled in the lower sections of the magma chamber, where they concentrated and formed Fe-Ti-V oxide ore layers at the base of the lower and upper cycles. Multiple episodes of magma replenishment in the magma chamber may have been involved in the formation of the Zhuqing intrusions.

  7. Finite element analysis of stress concentration in Class V restorations of four groups of restorative materials in mandibular premolar

    PubMed Central

    N, Shubhashini; N, Meena; Shetty, Ashish; Kumari, Anitha; DN, Naveen

    2008-01-01

    Aim: To study the concentration of stress in class V restoration of four different restorative materials subjected to occlusal load of 100N, 150N, 200N, 250N and to analyse the obtained data with the listed properties of the restorative material. Materials and Methods: Using FEM analysis the stresses generated in a class V lesion in a mandibular premolar was studied. Results: Within the framework of the aforementioned views, and from the results of the study it can be concluded that microfilled composite is the most suitable restorative material followed by flowable composite, glass ionomer cement and resin modified glass ionomer cement. Conclusion: Restoration of Class V lesions with materials of higher modulus of elasticity will enable better stress distribution. PMID:20142899

  8. Systems of elements preserving measure on varieties of groups

    SciTech Connect

    Timoshenko, E I

    2013-12-31

    It is proved that for any l, 1≤l≤r, a system of elements (v{sub 1},…,v{sub l}) of a free metabelian group S of rank r≥2 is primitive if and only if it preserves measure on the variety of metabelian groups A{sup 2}. From this we obtain the result that a system of elements (v{sub 1},…,v{sub l}) is primitive in the group S if and only if it is primitive in its profinite completion S-hat . Furthermore, it is proved that there exist a variety M and a nonprimitive element v∈F{sub r}(M) such that v preserves measure on M. Bibliography: 13 titles.

  9. Substantial enhancement in intrinsic coercivity on M-type strontium hexaferrite through the increase in magneto-crystalline anisotropy by co-doping of group-V and alkali elements

    SciTech Connect

    Ahn, Kyunghan Ryu, Byungki; Korolev, Dmitry; Jae Kang, Young

    2013-12-09

    The effect of d{sup 1} impurity doping in Sr-hexaferrite (SrM) on the magnetic anisotropy is investigated. First-principles calculations revealed that group-V elements (V, Nb) are stabilized with co-doping of alkali elements. Na{sup 1+}/K{sup 1+} doping at Sr{sup 2+}-site is found to be critical to form the d{sup 1} impurities at Fe-site. Experimentally, Na–V doped SrM shows the intrinsic coercivity of ∼5.4 kOe, which is ∼300% enhancement compared to undoped SrM and comparable value to La–Co co-doped SrM. Finally, the spin-orbit coupling from non-vanishing angular momentum of d{sup 1} impurity in SrM should be a main factor for such a substantial improvement of intrinsic coercivity.

  10. Cold Fusion Production and Decay of Neutron-Deficient Isotopes of Dubnium and Development of Extraction Systems for Group V Elements

    SciTech Connect

    Gates, Jacklyn M.

    2008-07-31

    Excitation functions for the 1n and 2n exit channels of the 208Pb(51V,xn)259-xDb reaction were measured. A maximum cross section of the 1n exit channel of 2070$+1100\\atop{-760}$ pb was measured at an excitation energy of 16.0 ± 1.8 MeV. For the 2n exit channel, a maximum cross section of 1660$+450\\atop{-370}$ pb was measured at 22.0 ± 1.8 MeV excitation energy. The 1n excitation function for the 209Bi(50Ti,n)258Db reaction was remeasured, resulting in a cross section of 5480$+1730\\atop{-1370}$ pb at an excitation energy of 16.0 ± 1.6 MeV. Differences in cross section maxima are discussed in terms of the fusion probability below the barrier. The extraction of niobium (Nb) and tantalum (Ta) from hydrochloric acid and mixed hydrochloric acid/lithium chloride media by bis(2-ethylhexyl) hydrogen phosphate (HDEHP) and bis(2-ethylhexyl) hydrogen phosphite (BEHP) was studied. The goal of the experiments was to find a system that demonstrates selectivity among the members of group five of the Periodic Table and is also suitable for the study of dubnium (Db, Z = 105). Experiments with niobium and tantalum were performed with carrier (10-6 M), carrier free (10-10 M) and trace (10-16 M) concentrations of metal using hydrochloric acid solution with concentrations ranging from 1 - 11 M. The extraction of niobium and tantalum from mixed hydrochloric acid/lithium chloride media by HDEHP and BEHP as a function of hydrogen ion (H+) concentration was also investigated. The data obtained are used as the basis to discuss the speciation of niobium and tantalum under the conditions studied and to evaluate possible extraction mechanisms. The 74Se(18O,p3n)88gNb excitation function was measured to determine the best energy for producing the 88Nb used in chemistry experiments. A maximum cross section of 495 +- 5 mb was observed at an 18O energy of 74.0 MeV

  11. Properties of Group Five and Group Seven transactinium elements

    SciTech Connect

    Wilk, Philip A.

    2001-05-01

    The detection and positive identification of the short-lived, low cross section isotopes used in the chemical studies of the heaviest elements are usually accomplished by measuring their alpha-decay, thus the nuclear properties of the heaviest elements must be examined simultaneously with their chemical properties. The isotopes 224 Pa and 266,267 Bh have been studied extensively as an integral part of the investigation of the heaviest members of the groups five and seven of the periodic table. The half-life of 224 Pa was determined to be 855 ±19 ms by measuring its alpha-decay using our rotating wheel, solid state detector system at the Lawrence Berkeley National Laboratory 88-Inch Cyclotron. Protactinium was produced by bombardment of a bismuth target. New neutron rich isotopes, 267 Bh and 266 Bh, were produced in bombardments of a 249 Bk target and their decay was observed using the rotating wheel system. The 266 Bh that was produced decays with a half-life of approximately 1 s by emission of alpha particles with an average energy of 9.25 plus/minus 0.03 MeV. 267 Bh was observed to decay with a 17 s half-life by emission of alpha-particles with an average energy of 8.83 plus/minus 0.03 MeV. The chemical behavior of hafnium, Ha (element 105) was investigated using the fast on-line continuous liquid extraction and detection system SISAK-LISSY. Hafnium was not observed in this experiment following transport and extraction. Protactinium was used as on-line test of the apparatus to determine the experimental efficiency of the entire system. Unfortunately, the amount of protactinium observed after the extraction, compared to the amount produced, was extremely small, only 2.5%. The extraction of the protactinium isotope indicated the efficiency of the apparatus was too low to observe the extraction of hafnium. The chemical behavior of oxychloride compounds of bohrium was

  12. Population responses to contour integration: early encoding of discrete elements and late perceptual grouping.

    PubMed

    Gilad, Ariel; Meirovithz, Elhanan; Slovin, Hamutal

    2013-04-24

    The neuronal mechanisms underlying perceptual grouping of discrete, similarly oriented elements are not well understood. To investigate this, we measured neural population responses using voltage-sensitive dye imaging in V1 of monkeys trained on a contour-detection task. By mapping the contour and background elements onto V1, we could study their neural processing. Population response early in time showed activation patches corresponding to the contour/background individual elements. However, late increased activity in the contour elements, along with suppressed activity in the background elements, enabled us to visualize in single trials a salient continuous contour "popping out" from a suppressed background. This modulated activity in the contour and in background extended beyond the cortical representation of individual contour or background elements. Finally, the late modulation was correlated with behavioral performance of contour saliency and the monkeys' perceptual report. Thus, opposing responses in the contour and background may underlie perceptual grouping in V1.

  13. Grouped element-by-element iteration schemes for incompressible flow computations

    NASA Astrophysics Data System (ADS)

    Tezduyar, T. E.; Liou, J.

    1989-05-01

    Grouped element-by-element (GEBE) iteration schemes for incompressible flows are presented in the context of vorticity- stream function formulation. The GEBE procedure is a variation of the EBE procedure and is based on arrangement of the elements into groups with no inter-element coupling within each group. With the GEBE approach, vectorization and parallel implementation of the EBE method becomes more clear. The savings in storage and CPU time are demonstrated with two unsteady flow problems.

  14. The Heavy Element Abundance in Groups of Galaxies

    NASA Technical Reports Server (NTRS)

    David, Laurence

    2000-01-01

    Over the past few years we have analyzed a sample of clusters observed by the Advanced Spacecraft for Cosmology Astrophysics (ASCA) X-ray satellite. We performed spatially resolved X-ray spectroscopy of a sample of 18 relaxed clusters of galaxies with gas temperatures below 4 keV. The spectral analysis was done using ASCA/SIS (Solid state Imaging Spectrometer) data combined with imaging data from ROSAT/PSPC (German acronym for X-ray satellite/Position Sensitive Proportional Counter) and Einstein/IPC (Imaging Proportional Counter) observations. We derived temperature profiles using single-temperature fits for all of the clusters in the sample, and also corrected for the presence of cold gas in the center of so-called 'cooling flow' clusters. For all of the clusters in the sample we derived Si and Fe abundance profiles. For a few of the clusters we also were able to derive Ne and S abundance profiles. We compared the elemental abundances derived at similar overdensities in all of the clusters in the sample. We also compared element mass-to-light ratios for the entire sample. We concluded that the preferential accretion of low entropy, low abundance gas into the potentials of groups and cold clusters can explain most of the observed trends in metallicity. In addition, we discussed the importance of preheating of the intracluster medium by Type II supernovae on the cluster scaling relations.

  15. Methods for forming group III-V arsenide-nitride semiconductor materials

    NASA Technical Reports Server (NTRS)

    Major, Jo S. (Inventor); Welch, David F. (Inventor); Scifres, Donald R. (Inventor)

    2000-01-01

    Methods are disclosed for forming Group III--arsenide-nitride semiconductor materials. Group III elements are combined with group V elements, including at least nitrogen and arsenic, in concentrations chosen to lattice match commercially available crystalline substrates. Epitaxial growth of these III-V crystals results in direct bandgap materials, which can be used in applications such as light emitting diodes and lasers. Varying the concentrations of the elements in the III-V crystals varies the bandgaps, such that materials emitting light spanning the visible spectra, as well as mid-IR and near-UV emitters, can be created. Conversely, such material can be used to create devices that acquire light and convert the light to electricity, for applications such as full color photodetectors and solar energy collectors. The growth of the III-V crystals can be accomplished by growing thin layers of elements or compounds in sequences that result in the overall lattice match and bandgap desired.

  16. Molecular beam epitaxy of III-P{sub x}As{sub 1−x} solid solutions: Mechanism of composition formation in the sublattice of a group V element

    SciTech Connect

    Emelyanov, E. A. Putyato, M. A.; Semyagin, B. R.; Feklin, D. F.; Preobrazhensky, V. V.

    2015-02-15

    The effect of substrate temperature, As{sub 2} and P{sub 2} molecular flux densities, and growth rate on the composition of III-P{sub x}As{sub 1−x} solid solution layers prepared by molecular beam epitaxy is experimentally investigated. Experimental data in a wide range of growth conditions are analyzed. The results obtained are presented in the form of a kinetic model for describing the process of formation of the composition in the Group V sublattice of the III-P{sub x}As{sub 1−x} solid solution upon molecular beam epitaxy. The model can be used for choosing the growth conditions of the III-P{sub x}As{sub 1−x} (001) solid-solution layers of a specified composition.

  17. Parallel and Serial Grouping of Image Elements in Visual Perception

    ERIC Educational Resources Information Center

    Houtkamp, Roos; Roelfsema, Pieter R.

    2010-01-01

    The visual system groups image elements that belong to an object and segregates them from other objects and the background. Important cues for this grouping process are the Gestalt criteria, and most theories propose that these are applied in parallel across the visual scene. Here, we find that Gestalt grouping can indeed occur in parallel in some…

  18. Parallel and serial grouping of image elements in visual perception.

    PubMed

    Houtkamp, Roos; Roelfsema, Pieter R

    2010-12-01

    The visual system groups image elements that belong to an object and segregates them from other objects and the background. Important cues for this grouping process are the Gestalt criteria, and most theories propose that these are applied in parallel across the visual scene. Here, we find that Gestalt grouping can indeed occur in parallel in some situations, but we demonstrate that there are also situations where Gestalt grouping becomes serial. We observe substantial time delays when image elements have to be grouped indirectly through a chain of local groupings. We call this chaining process incremental grouping and demonstrate that it can occur for only a single object at a time. We suggest that incremental grouping requires the gradual spread of object-based attention so that eventually all the object's parts become grouped explicitly by an attentional labeling process. Our findings inspire a new incremental grouping theory that relates the parallel, local grouping process to feedforward processing and the serial, incremental grouping process to recurrent processing in the visual cortex.

  19. Summary of the TeV33 working group

    SciTech Connect

    Bagley, P.P.; Bieniosek, F.M.; Colestock, P.

    1996-10-01

    This summary of the TeV33 working group at Snowmass reports on work in the areas of Tevatron store parameters, the beam-beam interaction, Main Injector intensity (slip stacking), antiproton production, and electron cooling.

  20. Determination of the CKM Element V(Ub)

    SciTech Connect

    Fortin, Dominique; /Victoria U.

    2007-04-06

    The precise determination of the CKM matrix element |V{sub ub}| is crucial in testing the Standard Model mechanism for CP violation. From a sample of 88 million B{bar B} pairs collected with the BABAR detector, charmless semileptonic B decays are selected using simultaneous requirements on the electron energy, E{sub e}, and the invariant mass squared of the electron-neutrino pair, q{sup 2}. The partial branching fraction, unfolded for detector effects, is determined in a region of the q{sup 2}-E{sub e} plane where the dominating semileptonic decays to charm mesons are highly suppressed. Theoretical calculations based on the Heavy Quark Expanion allows for a determination of |V{sub ub}| = (3.95 {+-} 0.27{sub -0.42}{sup +0.58} {+-} 0.25) x 10{sup -3}, where the errors represent experimental, heavy quark parameters and theoretical uncertainties, respectively.

  1. Platinum-group element abundance patterns in different mantle environments

    SciTech Connect

    Rehkaemper, M.; Halliday, A.N.; Barfod, D.; Fitton, J.G.; Dawson, J.B.

    1997-11-28

    Mantle-derived xenoliths from the Cameroon Line and northern Tanzania display differences in their platinum-group element (PGE) abundance patterns. The Cameroon Line lherzolites have uniform PGE patterns indicating a homogeneous upper mantle over several hundreds of kilometers, with approximately chondritic PGE ratios. The PGE patterns of the Tanzanian peridotites are similar to the PGE systematics of ultramafic rocks from ophiolites. The differences can be explained if the northern Tanzanian lithosphere developed in a fluid-rich suprasubduction zone environment, whereas the Cameroon Line lithosphere only experienced melt extraction from anhydrous periodotites. 32 refs., 2 figs., 1 tab.

  2. On spaces of commuting elements in Lie groups

    NASA Astrophysics Data System (ADS)

    Cohen, Frederick R.; Stafa, Mentor

    2016-11-01

    The main purpose of this paper is to introduce a method to stabilize certain spaces of homomorphisms from finitely generated free abelian groups to a Lie group $G$, namely $Hom(\\mathbb Z^n,G)$. We show that this stabilized space of homomorphisms decomposes after suspending once with summands which can be reassembled, in a sense to be made precise below, into the individual spaces $Hom(\\mathbb Z^n,G)$ after suspending once. To prove this decomposition, a stable decomposition of an equivariant function space is also developed. One main result is that the topological space of all commuting elements in a compact Lie group is homotopy equivalent to an equivariant function space after inverting the order of the Weyl group. In addition, the homology of the stabilized space admits a very simple description in terms of the tensor algebra generated by the reduced homology of a maximal torus in favorable cases. The stabilized space also allows the description of the additive reduced homology of the individual spaces $Hom(\\mathbb Z^n,G)$, with the order of the Weyl group inverted.

  3. Title V Operating Permit: CR Group, LLC - Tekoi Landfill

    EPA Pesticide Factsheets

    Final First Renewal of the Operating Permit (Permit Number: V-SV-000001-2016.00), Response to Public Comments and the Administrative Permit Record for the CR Group, LLC, Tekoi Landfill, located on the Skull Valley Indian Reservation, in Tooele County, UT.

  4. Intergenic transcription through a polycomb group response element counteracts silencing.

    PubMed

    Schmitt, Sabine; Prestel, Matthias; Paro, Renato

    2005-03-15

    Polycomb group response elements (PREs) mediate the mitotic inheritance of gene expression programs and thus maintain determined cell fates. By default, PREs silence associated genes via the targeting of Polycomb group (PcG) complexes. Upon an activating signal, however, PREs recruit counteracting trithorax group (trxG) proteins, which in turn maintain target genes in a transcriptionally active state. Using a transgenic reporter system, we show that the switch from the silenced to the activated state of a PRE requires noncoding transcription. Continuous transcription through the PRE induced by an actin promoter prevents the establishment of PcG-mediated silencing. The maintenance of epigenetic activation requires transcription through the PRE to proceed at least until embryogenesis is completed. At the homeotic bithorax complex of Drosophila, intergenic PRE transcripts can be detected not only during embryogenesis, but also at late larval stages, suggesting that transcription through endogenous PREs is required continuously as an anti-silencing mechanism to prevent the access of repressive PcG complexes to the chromatin. Furthermore, all other PREs outside the homeotic complex we tested were found to be transcribed in the same tissue as the mRNA of the corresponding target gene, suggesting that anti-silencing by transcription is a fundamental aspect of the cellular memory system.

  5. Grouping of contextual elements that affect vernier thresholds.

    PubMed

    Malania, Maka; Herzog, Michael H; Westheimer, Gerald

    2007-01-29

    To reveal the mechanisms of spatial interference in the fovea, we examined the capacity of a variety of lateral flanking configurations to interfere with alignment thresholds of a vertical vernier. A single line on each side of the vernier, at the optimal separation of 2-3 arcmin, raises thresholds threefold or more and masks most effectively when its length equals that of the vernier. For an array of equal lines whose length differs from that of the vernier, masking is reduced but not when vernier and flanks have the same length. The reduction for shorter and longer flanks can be reversed by inserting a gap in the row of flanks. By comparing the masking effect of arrays of mixed line lengths, we show that when a pair of flanks, which by itself masks strongly, becomes a component of a coherent contextual configuration, it loses much of its effectiveness to interact. Observers' ranking of the conspicuity of the vernier test pattern among the flanking elements is negatively correlated with the threshold elevation. We conclude that clustering of contextual patterns influences their capacity to mask. Discrimination of a target deteriorates when the target is grouped within an array of surrounding elements.

  6. Platinum group elements in the environment and their health risk.

    PubMed

    Ravindra, Khaiwal; Bencs, László; Van Grieken, René

    2004-01-05

    Accumulation of platinum group elements (PGEs) in the environment has been increased over the time. Catalytic converters of modern vehicles are considered to be the main sources of PGE pollution, since the correlation is between the Pt:Rh ratios in various environmental compartments and in converter units. The present literature survey shows that the concentration of these metals has increased significantly in the last decades in diverse environmental matrices; like airborne particulate matter, soil, roadside dust and vegetation, river, coastal and oceanic environment. Generally, PGEs are referred to behave in an inert manner and to be immobile. However, there is an evidence of spread and bioaccumulation of these elements in the environment. Platinum content of road dusts can be soluble, consequently, it enters the waters, sediments, soil and finally, the food chain. The effect of chronic occupational exposure to Pt compounds is well-documented, and certain Pt species are known to exhibit allergenic potential. However, the toxicity of biologically available anthropogenic Pt is not clear. Hence, there is a need to study the effect on human health of long-term chronic exposure to low levels of Pt compounds.

  7. The plant availability of auto-cast platinum group elements.

    PubMed

    Hooda, P S; Miller, A; Edwards, A C

    2008-04-01

    The introduction of automobile catalysts has raised environmental concern, as this pollution control technology is also an emission source for platinum group elements (PGE). The main aim of this study was to assess soil and grass PGE concentrations in soils adjacent to five road networks. The soil and grass samples were collected from four distances at each site; they were 0, 1, 2 and 5 m from the road edges. The maximum soil Pt, Rh and Pd concentrations were measured at the road perimeters. Pd concentrations were much higher than Pt or Rh, possibly due to differences in its use, emission and/or soil chemistry. Rh and Pt soil concentrations accounted for 66 and 34% (P < 0.01) of the variability observed, respectively, in their plant concentrations. Grass Pd concentrations had no relationship with its total soil concentrations.

  8. Mahowaldean families of elements in stable homotopy groups revisited

    NASA Astrophysics Data System (ADS)

    Hunter, David J.; Kuhn, Nicholas J.

    1999-09-01

    In the mid 1970s Mark Mahowald constructed a new infinite family of elements in the 2-component of the stable homotopy groups of spheres, [eta]j[set membership][pi]Sj2 (S0)(2) [M]. Using standard Adams spectral sequence terminology (which will be recalled in Section 3 below), [eta]j is detected by h1hj[set membership]Ext2,*[script A] (Z/2, Z/2). Thus he had found an infinite family of elements all having the same Adams filtration (in this case, 2), thus dooming the so-called Doomsday Conjecture. His constructions were ingenious: his elements were constructed as composites of pairs of maps, with the intermediate spaces having, on one hand, a geometric origin coming from double loopspace theory and, on the other hand, mod2 cohomology making them amenable to Adams Spectral Sequence analysis and suggesting that they were related to the new discovered Brown-Gitler spectra [BG].In the years that followed, various other related 2-primary infinite families were constructed, perhaps most notably (and correctly) Bruner's family detected by h2h2j[set membership] Ext3,*[script A](Z/2, Z/2) [B]. An odd prime version was studied by Cohen [C], leading to a family in [pi]S[low asterisk](S0)(p) detected by h0bj[set membership] Ext3,*[script A] (Z/p, Z/p) and a filtration 2 family in the stable homotopy groups of the odd prime Moore space. Cohen also initiated the development of odd primary Brown-Gitler spectra, completed in the mid 1980s, using a different approach, by Goerss [G], and given the ultimate ‘modern’ treatment by Goerss, Lannes and Morel in the 1993 paper [GLM]. Various papers in the late 1970s and early 1980s, e.g. [BP, C, BC], related some of these to loopspace constructions.Our project originated with two goals. One was to see if any of the later work on Brown-Gitler spectra led to clarification of the original constructions. The other was to see if taking advantage of post Segal Conjecture knowledge of the stable cohomotopy of the classifying space BZ/p would

  9. Thermodynamic properties of the Group 1A elements

    SciTech Connect

    Alcock, C.B.; Itkin, V.P.; Chase, M.W.

    1994-05-01

    This review describes thermodynamic properties of condensed phases of the alkali metals, excluding francium for which the amount of information is too limited. The properties considered are: heat capacities from 0 to 1600 K, temperatures and enthalpies of fusion and martensitic transformation in Li and Na; discussion of the Debye temperature and electronic heat capacity coefficient at absolute zero temperature is also included. The paper is the second part of a series. Similar to previous assessment of the IIA group [93ALC/CHA], this paper considers original studies, especially with respect to factors which influence the accuracy and reliability of results. Recommendations derived from such analyses are compared with most advanced previous reviews made at the Institute for High Temperatures (Moscow) [70SHP/YAK], [82GUR] and the National Institute of Standards and Technology (Washington) [85JAN]. The properties of individual elements of the group are compared and suggestions are made for experimental studies which should improve poorly measured quantities. The review is supplemented by an IBM PC database which contains references, assessed data, brief description of studies and has facilities for fitting and plotting of data and for adding new information.

  10. Comprehensive Analyses of the Spectra of Iron-group Elements

    NASA Astrophysics Data System (ADS)

    Nave, Gillian; Sansonetti, Craig J; Pickering, Juliet C; Liggins, Florence

    2014-06-01

    For many decades, the Atomic Spectroscopy Group at NIST has measured atomic data of vital use to astronomy and other fields using high resolution spectrometers that are found in few other places in the world. These now include the 2-m Fourier transform (FT) spectrometer covering the region 285 nm to 5500 nm, the FT700 vacuum ultraviolet (VUV) FT spectrometer covering the region 143 nm to 900 nm, and a 10.7-m normal incidence spectrograph (NIVS) covering 30 nm to 500 nm. Recent work focused on the measurement and analysis of wavelengths and energy levels of iron-group elements to provide extensive data for the analysis of astrophysical spectra. Our comprehensive linelist for Fe II from 90 nm to 5500 nm contains over 13 600 lines with order of magnitude improvements in the wavelengths compared to previous work [Nave & Johansson, ApJSS 204, 1(2013)]. The spectra were observed in high-current continuous and pulsed hollow cathode (HCL) discharges using FT spectrometers and our NIVS spectrograph. A similar analysis of Cr II contains over 5300 lines and extends the knowledge of this spectrum to the previously unobserved region between 731 nm at 5500 nm [Sansonetti, Nave, Reader & Kerber, ApJSS 202, 15 (2012); Sansonetti & Nave, ApJSS (in prep.)]. Our analysis of the Co III spectrum contains 750 lines observed in Penning discharge lamps and an additional 900 lines compiled from previous work, including Ritz wavelengths, optimized energy levels, and calculated log(gf) values [Smillie, Pickering, Nave & Smith, ApJSS (in prep.)]. NIST and ICL are currently collaborating to complete the measurement and analysis of wavelengths, energy levels, and hyperfine structure parameters for all singly-ionized iron-group elements of astrophysical interest, covering the wavelength range 80 nm to 5500 nm. This project uses archival data from FT spectrometers at NIST, ICL and Kitt Peak National Observatory, with additional spectra of HCL and Penning discharge sources taken using our FT and

  11. Method of fabricating vertically aligned group III-V nanowires

    DOEpatents

    Wang, George T; Li, Qiming

    2014-11-25

    A top-down method of fabricating vertically aligned Group III-V micro- and nanowires uses a two-step etch process that adds a selective anisotropic wet etch after an initial plasma etch to remove the dry etch damage while enabling micro/nanowires with straight and smooth faceted sidewalls and controllable diameters independent of pitch. The method enables the fabrication of nanowire lasers, LEDs, and solar cells.

  12. Platinum-group elements: so many excellent properties

    USGS Publications Warehouse

    Zientek, Michael L.; Loferski, Patricia J.

    2014-01-01

    The platinum-group elements (PGE) include platinum, palladium, rhodium, ruthenium, iridium, and osmium. These metals have similar physical and chemical properties and occur together in nature. The properties of PGE, such as high melting points, corrosion resistance, and catalytic qualities, make them indispensable to many industrial applications. PGE are strategic and critical materials for many nations because they are essential for important industrial applications but are mined in a limited number of places and have no adequate substitutes. Exploration and mining companies have found approximately 104,000 metric tons of PGE (with minor gold) in mineral deposits around the world that could be developed. For PGE, almost all known production and resources are associated with three geologic features: the Bushveld Complex, a layered mafic-to-ultramafic intrusion in South Africa; the Great Dyke, a layered mafic-to-ultramafic intrusion in Zimbabwe; and sill-like intrusions associated with flood basalts in the Noril’sk-Talnakh area, Russia. To help predict where PGE supplies might be located, USGS scientists study how and where PGE resources are concentrated in the Earth's crust and use that knowledge to assess the likelihood that undiscovered PGE deposits may exist. Techniques used for assessing mineral resources were developed by the USGS to support the stewardship of Federal lands and evaluate mineral resource availability in a global context. The USGS also compiles statistics and information on the worldwide supply, demand, and flow of PGE. These data are all used to inform U.S. national policymakers.

  13. Investigation of group IVA elements combined with HAXPES and first-principles calculations

    NASA Astrophysics Data System (ADS)

    Cui, Y.-T.; Li, G.-L.; Oji, H.; Son, J.-Y.

    2014-04-01

    The core level and valence band spectra of group IVA elements were investigated with hard x-ray photoemission spectroscopy (HAXPES) photon energy of 7.939 keV by bulk sensitive manner. The survey and valance band spectra were presented, relative peaks intensity are discussed by thinking about inelastic mean free path (IMFP) and photoionization cross section of photoelectrons (PICS). In order to understand bulk band structures, valence bands are compared with the calculated ones by considering PICS, IMFP and total energy resolution. The calculated results by GGA, HSE06 and GW0 methods are simply discussed by comparing with experiment spectra.

  14. Platinum group elements in airborne particles in Mexico City.

    PubMed

    Rauch, Sebastien; Peucker-Ehrenbrink, Bernhard; Molina, Luisa T; Molina, Mario J; Ramos, Rafael; Hemond, Harold F

    2006-12-15

    Automobile exhaust catalysts using platinum group elements (PGE) have been mandatory on new cars in the Mexico City Metropolitan Area (MCMA) since 1991. Platinum, Pd, Rh, Ir, and Os concentrations and the isotopic composition of Os were determined in PM10 samples from the MCMA. Samples were prepared by isotope dilution NiS fire assay, and analysis was performed by magnetic sector ICP-MS using a single collector instrument for Pt, Pd, Rh, and Ir analysis and a multicollector instrument for Os analysis. Pt, Pd, and Rh concentrations at a downtown location (Merced) increased from < or =1.7 pg of Pt m(-3), 2.7 (4.0) pg of Pd m(-3), and 1.2+/-0.9 pg of Rh m(-3) in 1991 to 9.6 +/- 1.8 pg of Pt m(-3), 10.2+/-1.8 pg of Pd m(-3), and 2.8 +/-0.6 pg of Rh m(-3) in 2003. Concentrations at five sites in MCMA in 2003 averaged 9.3+/-1.9 pg of Pt m(-3), 11+/-4 pg of Pd m(-3), and 3.2+/- 1.0 pg of Rh m(-3). In contrast, Ir and Os concentrations and Os isotopic composition remained relatively constant and were 0.08+/-0.04 pg of Ir m(-3), 0.030 +/-0.007 pg of Os m(-3), and 0.60+/-0.04, respectively, in the MCMA in 2003. Elevated Pt, Pd, and Rh concentrations in the MCMA are attributed to automobile catalysts. A Pt-Pd-Rh concentration peak in 1993 suggests that early catalysts emitted a larger amount of PGE, possibly due to factors inherent in the technology or the use of inappropriate gasoline. Therefore, this study suggests that the current introduction of automobile catalysts in developing countries may result in elevated PGE concentrations if it is not accompanied by infrastructures and policy measures supporting their efficient use.

  15. Bioaccessibility of platinum group elements in automotive catalytic converter particulates.

    PubMed

    Turner, Andrew; Price, Simon

    2008-12-15

    The bioaccessibilities of the platinum group elements (PGE): Rh, Pd, and Pt; and the catalyzator poison, Pb, have been determined in particles derived from milled automotive catalytic converters using a physiologically based extraction test (PBET) that simulates, sequentially, the chemical conditions encountered in the human stomach and intestine. PGE accessibility, relative to total metal concentration, was generally less than a few percent, but increased in the stomach with decreasing pH (from 4 to 1) and/or increasing chloride concentration, and with decreasing particle concentration. In most cases, bioaccessibility increased from the acidic stomach to the neutral, carbonate-rich intestine. Bioaccessibility of Pb displayed similar pH and particle concentration dependencies to PGE in the stomach, but this metal exhibited significantly greater mobilization (up to 80%) overall and a reduction in accessibility from the stomach to intestine. Reaction kinetics of PGE dissolution in the stomach at pH 2.5 were modeled using a combined surface reaction-diffusion controlled mechanism with rate constants of 0.068, 0.031, and 0.015 (microg L(-1))(-1) h(-1) for Rh, Pd, and Pt, respectively. For Pb, however, mobilization proceeded via a different mechanism whose time-dependence was fitted with an empirical, logarithmic equation. Overall, PGE bioaccessibility appeared to be controlled by dissolution rates of metallic nanoparticles in the stomach, and solubility and kinetic constraints on inorganic species (chlorides, hydroxychlorides, and carbanatochlorides) and undefined organic complexes formed in the simulated gastrointestinal tract. Further studies are required to elucidate any effects engendered by the long-term oral exposure of small quantities of these species.

  16. Fe-Group Elements in the Metal-Poor Star HD 84937: Abundances and their Implications

    NASA Astrophysics Data System (ADS)

    Sneden, Chris; Cowan, John J.; Kobayashi, Chiaki; Pignatari, Marco; Lawler, James E.; Den Hartog, Elizabeth; Wood, Michael P.

    2016-01-01

    We have derived accurate relative abundances of the Fe-group elements Sc through Zn in the very metal-poor main-sequence turnoff star HD 84937. For this study we analyzed high resolution, high signal-to-noise HST/STIS and VLT/UVES spectra over a total wavelength range 2300-7000 Å. We employed only recent or newly-applied reliable laboratory transition data for all species. Abundances from more than 600 lines of non-Fe species were combined with about 550 Fe lines in HD 84937 to yield abundance ratios of high precision. From parallel analyses of solar photospheric spectra we also derived new solar abundances of these elements. This in turn yielded internally-consistent relative HD 84937 abundances with respect to the Sun. For seven of the ten Fe-group elements the HD 84937 abundances were from both neutral and ionized transitions. In all of these cases the neutral and ionized species yield the same abundances within the measurement uncertainties. Therefore standard Saha ionization balance appears to hold in the HD 84937 atmosphere. We derived metallicity [Fe/H] = -2.32 with sample standard deviation of 0.06. Solid evidence is seen for departures from the solar abundance mix in HD 84937, for example [Co/Fe] = +0.14, [Cu/Fe] = -0.83, and <[Sc,Ti,V/Fe]> = +0.31. Combining our Sc, Ti, and V abundances for this star with those from large-sample spectroscopic surveys suggests that these elements are positively correlated in stars with [Fe/H] < -2. HD 84937 is unusually enriched in Sc, Ti, and V. Our analysis strongly suggests that different types of supernovae with a large scatter of explosion energies and asymmetries contributed to the creation of the Fe-group elements early in the Galaxy's history.This work has been supported in part by NASA grant NNX10AN93G (J.E.L.), by NSF grants AST-1211055 (J.E.L.), AST-1211585 (C.S.), PHY-1430152 (through JINA, J.J.C. and M.P.), EU MIRGCT-2006-046520 (M.P.), and by the ``Lendlet-2014'' Programme of the Hungarian Academy of

  17. Sandia Higher Order Elements (SHOE) v 0.5 alpha

    SciTech Connect

    2013-09-24

    SHOE is research code for characterizing and visualizing higher-order finite elements; it contains a framework for defining classes of interpolation techniques and element shapes; methods for interpolating triangular, quadrilateral, tetrahedral, and hexahedral cells using Lagrange and Legendre polynomial bases of arbitrary order; methods to decompose each element into domains of constant gradient flow (using a polynomial solver to identify critical points); and an isocontouring technique that uses this decomposition to guarantee topological correctness. Please note that this is an alpha release of research software and that some time has passed since it was actively developed; build- and run-time issues likely exist.

  18. New laboratory atomic data for neutral, singly and doubly ionised iron group elements for astrophysics applications

    NASA Astrophysics Data System (ADS)

    Pickering, Juliet C.; Nave, Gillian; Liggins, Florence; Clear, Christian; Ruffoni, Matthew; Sansonetti, Craig

    2015-08-01

    We present new laboratory spectroscopic measurements to produce atomic data for astrophysically important species: neutral, singly and doubly ionised iron group elements.We use high resolution Fourier Transform Spectrometry (FTS) (resolving power up to 2x106 at 200nm) to measure atomic spectra, giving accurate line wavelengths (to a few parts in 108), atomic energy levels, hyperfine structure splitting and log gfs (accurate to a few %) (Ruffoni et al this meeting). These data are vital for astrophysical spectral analyses for: line identification, spectrum synthesis, elemental abundance determinations [eg 1], and disentangling of blends etc. It is not possible to theoretically calculate these atomic data to the accuracy needed for modern astrophysics applications.At Imperial College we have a unique visible-VUV FT spectrometer with short wavelength cut-off of 135nm. We supplement FTS data at shorter wavelengths with spectra recorded on the NIST 10.7m grating spectrograph (with phosphor image or photographic plates) and at longer wavelengths in the IR we use the NIST IR FT spectrometer.An elemental spectrum may contain thousands of spectral lines from the IR to VUV. We use these wavelengths to correct known atomic energy levels, and search for new atomic levels. The result is a classified linelist and accurate atomic energy levels.We present progress on iron group element atomic energy levels and wavelengths for V I and V II [2,3], Co III [4], Cr I, Mn I and Mn II, and Ni II.This work is supported by STFC(UK), The Leverhulme Trust, The Royal Society and NASA.References[1] Bergemann M, Pickering JC & Gehren T,“NLTE analysis of Co I/Co II lines in spectra of cool stars with new laboratory hyperfine splitting constants",MNRAS 401(2) 1334 (2010)[2] Thorne AP, Pickering JC & Semeniuk J,“The spectrum and term analysis of V II”, ApJS 207,13 (2013)[3] Thorne AP, Pickering JC & Semeniuk J,“The spectrum and term analysis of V I",ApJS 192,11 (2011)[4] Smillie DG

  19. The elemental composition of the Sun. II. The iron group elements Sc to Ni

    NASA Astrophysics Data System (ADS)

    Scott, Pat; Asplund, Martin; Grevesse, Nicolas; Bergemann, Maria; Sauval, A. Jacques

    2015-01-01

    We redetermine the abundances of all iron group nuclei in the Sun, based on neutral and singly-ionised lines of Sc, Ti, V, Mn, Fe, Co and Ni in the solar spectrum. We employ a realistic 3D hydrodynamic model solar atmosphere, corrections for departures from local thermodynamic equilibrium (NLTE), stringent line selection procedures and high quality observational data. We have scoured the literature for the best quality oscillator strengths, hyperfine constants and isotopic separations available for our chosen lines. We find log ɛSc = 3.16 ± 0.04, log ɛTi = 4.93 ± 0.04, log ɛV = 3.89 ± 0.08, log ɛCr = 5.62 ± 0.04, log ɛMn = 5.42 ± 0.04, log ɛFe = 7.47 ± 0.04, log ɛCo = 4.93 ± 0.05 and log ɛNi = 6.20 ± 0.04. Our uncertainties factor in both statistical and systematic errors (the latter estimated for possible errors in the model atmospheres and NLTE line formation). The new abundances are generally in good agreement with the CI meteoritic abundances but with some notable exceptions. This analysis constitutes both a full exposition and a slight update of the preliminary results we presented in Asplund et al. (2009, ARA&A, 47, 481), including full line lists and details of all input data we employed. Tables 1-3 are available in electronic form at http://www.aanda.org

  20. Elements of Mathematics, Book 10: Groups and Rings.

    ERIC Educational Resources Information Center

    Exner, Robert; And Others

    One of 12 books developed for use with the core material (Book O) of the Elements of Mathematics Program, this text covers material well beyond the scope of the usual secondary mathematics sequences. These materials are designed for highly motivated students with strong verbal abilities; mathematical theories and ideas are developed through…

  1. Comprehensive Wavelengths, Energy Levels, and Hyperfine Structure Parameters of Singly-Ionized Iron-Group Elements

    NASA Astrophysics Data System (ADS)

    Nave, Gillian

    We propose to measure wavelengths, energy levels, and hyperfine structure parameters of Ni II, Mn II, Sc II and other singly-ionized iron-group elements, covering the wavelength range 80 nm to 5500 nm. We shall use archival data from spectrometers at NIST and Kitt Peak National Observatory for spectra above 140 nm. Additional experimental observations will be taken if needed using Fourier transform spectrometers at NIST. Spectra will be taken using our normal incidence grating spectrograph to provide better sensitivity than the FT spectra and to extend the wavelength range down to 80 nm. We aim to produce a comprehensive description of the spectra of all singly-ionized iron- group elements. The wavelength uncertainty of the strong lines will be better than 1 part in 10^7. For most singly-ionized iron-group elements available laboratory data have uncertainties an order of magnitude larger than astronomical observations over wide spectra ranges. Some of these laboratory measurements date back to the 1960's. Since then, Fourier transform spectroscopy has made significant progress in improving the accuracy and quantity of data in the UV-vis-IR region, but high quality Fourier transform spectra are still needed for Mn II, Ni II and Sc II. Fourier transform spectroscopy has low sensitivity in the VUV region and is limited to wavelengths above 140 nm. Spectra measured with high-resolution grating spectrographs are needed in this region in order to obtain laboratory data of comparable quality to the STIS and COS spectrographs on the Hubble Space Telescope. Currently, such data exist only for Fe II and Cr II. Lines of Sc II, V II, and Mn II show hyperfine structure, but hyperfine structure parameters have been measured for relatively few lines of these elements. Significant errors can occur if hyperfine structure is neglected when abundances are determined from stellar spectra. Measurements of hyperfine structure parameters will be made using Fourier transform spectroscopy

  2. Integrated learning in practical machine element design course: a case study of V-pulley design

    NASA Astrophysics Data System (ADS)

    Tantrabandit, Manop

    2014-06-01

    To achieve an effective integrated learning in Machine Element Design course, it is of importance to bridge the basic knowledge and skills of element designs. The multiple core learning leads the pathway which consists of two main parts. The first part involves teaching documents of which the contents are number of V-groove formulae, standard of V-grooved pulleys, and parallel key dimension's formulae. The second part relates to the subjects that the students have studied prior to participating in this integrated learning course, namely Material Selection, Manufacturing Process, Applied Engineering Drawing, CAD (Computer Aided Design) animation software. Moreover, an intensive cooperation between a lecturer and students is another key factor to fulfill the success of integrated learning. Last but not least, the students need to share their knowledge within the group and among the other groups aiming to gain knowledge of and skills in 1) the application of CAD-software to build up manufacture part drawings, 2) assembly drawing, 3) simulation to verify the strength of loaded pulley by method of Finite Element Analysis (FEA), 4) the software to create animation of mounting and dismounting of a pulley to a shaft, and 5) an instruction manual. The end product of this integrated learning, as a result of the above 1 to 5 knowledge and skills obtained, the participating students can create an assembly derived from manufacture part drawings and a video presentation with bilingual (English-Thai) audio description of Vpulley with datum diameter of 250 mm, 4 grooves, and type of groove: SPA.

  3. Transferable tight binding model for strained group IV and III-V heterostructures

    NASA Astrophysics Data System (ADS)

    Tan, Yaohua; Povolotskyi, Micheal; Kubis, Tillmann; Boykin, Timothy; Klimeck, Gerhard

    Modern semiconductor devices have reached critical device dimensions in the range of several nanometers. For reliable prediction of device performance, it is critical to have a numerical efficient model that are transferable to material interfaces. In this work, we present an empirical tight binding (ETB) model with transferable parameters for strained IV and III-V group semiconductors. The ETB model is numerically highly efficient as it make use of an orthogonal sp3d5s* basis set with nearest neighbor inter-atomic interactions. The ETB parameters are generated from HSE06 hybrid functional calculations. Band structures of strained group IV and III-V materials by ETB model are in good agreement with corresponding HSE06 calculations. Furthermore, the ETB model is applied to strained superlattices which consist of group IV and III-V elements. The ETB model turns out to be transferable to nano-scale hetero-structure. The ETB band structures agree with the corresponding HSE06 results in the whole Brillouin zone. The ETB band gaps of superlattices with common cations or common anions have discrepancies within 0.05eV.

  4. The Abundances of the Fe Group Elements in Early B Stars in the Magellanic Clouds and Bridge

    NASA Astrophysics Data System (ADS)

    Peters, Geraldine J.; Adelman, Saul J.

    2016-01-01

    The abundances of three Fe Group elements (V, Cr, and Fe) in 9 early main-sequence band B stars in the LMC, 7 in the SMC , and two in the Magellanic Bridge have been determined from archival FUSE observations and the Hubeny/Lanz NLTE programs TLUSTY/SYNSPEC. Lines from the Fe group elements, except for a few weak multiplets of Fe III, are not observable in the optical spectral region. The best set of lines in the FUSE spectral region are Fe III (UV1), V III 1150 Å, and Cr III 1137 Å. The abundances of these elements in early B stars are a marker for recent SNe Ia activity, as a single exploding white dwarf can deliver 0.5 solar masses of Ni-56 that decays into Fe to the ISM. The Fe group abundances in an older population of stars primarily reflect SNe II activity, in which a single explosion delivers only 0.07 solar masses of Ni-56 to the ISM (the rest remains trapped in the neutron star). The abundances of the Fe group elements in early B stars not only track SNe Ia activity but are also important for computing evolutionary tracks for massive stars. In general, the Fe abundance relative to the sun's value is comparable to the mean abundances for the lighter elements in the Clouds/Bridge but the values of [V,Cr/Fe]sun are smaller. This presentation will discuss the spatial distribution of the Fe Group elements in the Magellanic Clouds, and compare it with our galaxy in which the abundance of Fe declines with radial distance from the center. Support from NASA grants NAG5-13212, NNX10AD66G, STScI HST-GO-13346.22, and USC's Women in Science and Engineering (WiSE) program is greatly appreciated.

  5. Design, synthesis, and properties of phthalocyanine complexes with main-group elements showing main absorption and fluorescence beyond 1000 nm.

    PubMed

    Furuyama, Taniyuki; Satoh, Koh; Kushiya, Tomofumi; Kobayashi, Nagao

    2014-01-15

    We present a comprehensive description of the unique properties of newly developed phthalocyanines (Pcs) containing main-group elements that absorb and emit in the near-IR region. Group 16 (S, Se, and Te) elements and group 15 (P, As, and Sb) elements were used as peripheral and central (core) substituents. With the introduction of group 16 elements into free-base Pc, a red-shift of the Q-band was observed, as a result of the electron-donating ability of group 16 elements particularly at the α positions. An X-ray crystallographic analysis of α-ArS-, ArSe-, and ArTe-linked free-base Pcs was also successfully performed, and the relationship between structure and optical properties was clarified. When a group 15 element ion was introduced into the center of the Pc ring, the resulting Pcs showed a single Q-band peak beyond 1000 nm (up to 1056 nm in CH2Cl2). In particular, [(ArS)8PcP(OMe)2](+) and [(ArS)8PcAs(OMe)2](+) exhibited a distinct fluorescence in the 960-1400 nm region with moderate quantum yields. The atomic radius of the group 15 element is important for determining the Pc structure, so that this can be controlled by the choice of group 15 elements. Electrochemical data revealed, while MO calculations suggested, that the red-shift of the Q-band is attributable to a decrease of the HOMO-LUMO gap due to significant and moderate stabilization of the LUMO and HOMO, respectively. The effect of peripheral substutuents and a central P(V) ion on the Q-band shift was independently predicted by MO calculations, while the magnitude of the total calculated shift was in good agreement with the experimental observations. The combination of spectral, electrochemical, and theoretical considerations revealed that all of the central group 15 elements, peripheral group 16 elements, and their positions are necessary to shift the Q-band beyond 1000 nm, indicating that the substitution effects of group 15 and 16 elements act synergistically. The Pcs having Q-bands beyond 1000 nm

  6. Trace element seasonality in marine macroalgae of different functional-form groups.

    PubMed

    Malea, Paraskevi; Chatziapostolou, Anastasia; Kevrekidis, Theodoros

    2015-02-01

    Novel information on the seasonality of element accumulation in seaweeds is provided. Seasonal patterns of As, Ba, Cd, Co, Cr, Cu, Mn, Mo, Ni, Pb, Se, Sr, U, V and Zn concentrations in macroalgae belonging to different functional-form groups (Ulva intestinalis, Ulva rigida, Codium fragile, Gracilaria gracilis) from the Thessaloniki Gulf, Aegean Sea were determined and compared. Uni- and multivariate data analyses were applied. Element concentrations generally decreased during spring and/or summer, probably due to the growth effect, but a reverse trend, particularly in Ulva species, was also observed. Most elements (Cd, Co, Cr, Cu, Mo, Ni, Pb, Sr) in Ulva species displayed a comparatively low monthly variability, indicating that the extent of seasonal variation is closely related to thallus morphology and growth strategy. In particular, these data suggest that Cd, Co, Cr, Cu, Mo, Ni, Pb and Sr contents in fast-growing, sheet-like macroalgae are less influenced by the season, compared to their contents in coarsely-branched and thick-leathery macroalgae; therefore, sheet-like macroalgae may be more appropriate to be used in biomonitoring of coastal waters. The data presented could be utilized in the development of biomonitoring programmes for the protection of coastal environments.

  7. Electron collisions with Fe-peak elements: Fe V

    NASA Astrophysics Data System (ADS)

    McLaughlin, B. M.; Norrington, P. H.; Hibbert, A.; Scott, M. P.; Burke, P. G.; Burke, V. M.; Noble, C. J.

    2006-05-01

    Lines of Fe^+ -- Fe^6+ ions appear in the UV spectra of O-type stars. Accurate assessments of the relevant abundances of heavy elements and their ions can be obtained from the comparison of the observed spectra with synthetic NLTE spectra, if the atomic data for electron and photon interaction processes are known with sufficient accuracy. Electron-impact excitation collision strengths for the Fe-peak element Fe^4+ are calculated in the close-coupling approximation using the R-matrix suite of codes PRMAT. Eighty LS - coupled states arising from the 3d^4, 3d^34s and 3d^34p configurations of Fe^4+ are retained in our calculations. Accurate multi-configuration interaction target and scattering wavefunctions are used with the aid of 3p^2 ->3d^2 two-electron promotions and a n=4 basis set. Effective collision strengths for optically forbidden transitions in the 3d^4 manifold, which are extremely important in the analysis of lines in the Fe^4+ spectra, are obtained by averaging the electron collision strengths over a Maxwellian distribution for the electron temperature. The present results when compared to previous investigations for temperatures below 100,000 Kelvin show an enhancement of a factor of two. Further details will be presented at the meeting.

  8. On Spaces of Commuting Elements in Lie Groups

    DTIC Science & Technology

    2014-02-25

    Zn;G) follows from that of Comm(G) for any cohomology theory. The results for singular homology of Comm(G) are given in terms of the tensor algebra ...cohomology theory. The results for singular homology of Comm(G) are given in terms of the tensor algebra generated by the reduced homology of a maximal...components, for π the fundamental group of a closed oriented surface and G a finite cover of a projective special linear group. For non-negative integers n

  9. Two-Element Generation of Unitary Groups Over Finite Fields

    DTIC Science & Technology

    2013-01-31

    like to praise my Lord and Savior, Jesus Christ , for allowing me this opportunity to work on a Ph.D in mathematics, and for His sustaining grace...Ishibashi’s original result. The paper’s main theorem will show that all unitary groups over finite fields of odd characteristic are generated by only two

  10. Theoretical predictions of properties of group-2 elements including element 120 and their adsorption on noble metal surfaces.

    PubMed

    Pershina, V; Borschevsky, A; Anton, J

    2012-04-07

    Trends in properties of group-2 elements Ca through element 120 and their M(2) and MAu dimers were determined on the basis of atomic and molecular relativistic density functional theory calculations. The relativistic contraction and stabilization of the ns AO with increasing atomic number were shown to result in the inversion of trends both in atomic and molecular properties in group 2 beyond Ba, so that element 120 should be chemically similar to Sr. Due to the same reason, bonding in (120)(2) and 120Au should be the weakest among the considered here M(2) and MAu. Using calculated dissociation energies of M(2), the sublimation enthalpy, ΔH(sub), of element 120 of 150 kJ/mol was estimated via a correlation between these quantities in group 2. Using the M-Au binding energies, the adsorption enthalpies, ΔH(ads), of element 120 of 172 kJ/mol on gold, 127 kJ/mol on platinum, and 50 kJ/mol on silver were estimated via a correlation with known ΔH(ads) in the group. These moderate values of ΔH(ads) are indicative of a possibility of chromatography adsorption studies of element 120 on these noble metal surfaces.

  11. Dimers of heavy p-elements of groups IV-VI: Electronic, vibrational, and magnetic properties

    NASA Astrophysics Data System (ADS)

    Borisova, S. D.; Rusina, G. G.; Eremeev, S. V.; Chulkov, E. V.

    2016-04-01

    Equilibrium lengths and binding energies, vibrational frequencies, width of the HOMO-LUMO gap, and the magnetic anisotropy energies for one- and two-component dimers of heavy p elements of Groups IV (Sn, Pb), V (Sb, Bi), and VI (Se, Te) with a pronounced relativistic effect have been calculated with the use of the formalism of the density functional theory. It has been shown that it is necessary to take into account the spin-orbit coupling, which significantly affects the energy parameters of clusters. The analysis of the data obtained has revealed that the Pb-Te, Pb-Se, Sn-Te, and Sn-Se dimers have the widest gap at the Fermi level and the lowest reactivity. The magnetic anisotropy energy has been calculated for all single- and doublecomponent dimers and the direction of the easy magnetization axis has been determined.

  12. Report of the IAU/IAG Working Group on cartographic coordinates and rotational elements: 2006

    USGS Publications Warehouse

    Seidelmann, P.K.; Archinal, B.A.; A'Hearn, M.F.; Conrad, A.; Consolmagno, G.J.; Hestroffer, D.; Hilton, J.L.; Krasinsky, G.A.; Neumann, G.; Oberst, J.; Stooke, P.; Tedesco, E.F.; Tholen, D.J.; Thomas, P.C.; Williams, I.P.

    2007-01-01

    Every three years the IAU/IAG Working Group on Cartographic Coordinates and Rotational Elements revises tables giving the directions of the poles of rotation and the prime meridians of the planets, satellites, minor planets, and comets. This report introduces improved values for the pole and rotation rate of Pluto, Charon, and Phoebe, the pole of Jupiter, the sizes and shapes of Saturn satellites and Charon, and the poles, rotation rates, and sizes of some minor planets and comets. A high precision realization for the pole and rotation rate of the Moon is provided. The expression for the Sun's rotation has been changed to be consistent with the planets and to account for light travel time ?? 2007 Springer Science+Business Media B.V.

  13. Vapor phase growth of group 3, 4, and 5 compounds by HCl transport of elements

    NASA Technical Reports Server (NTRS)

    Tyagi, R. C.; Debnam, W. J., Jr.; Mcnear, M. F.; Crouch, R. K.; Breckenridge, R. A.

    1973-01-01

    Technique has been devised for vapor-phase epitaxial growth of group 3, 4, and 5 binary, ternary, or quaternary compounds by HCl transport of the constituent elements or dopants. Technique uses all the constituents of the alloy system in their elemental form. Transport of these elements by an HCl + H2 carrier gas facilitates their transport as subchlorides.

  14. X-ray standing wave investigations of Group III and V metal adsorption on Si(001)

    SciTech Connect

    Qian, Y.; Bedzyk, M.J. |; Lyman, P.F.

    1997-05-01

    Investigations of atomic bonding, surface reconstruction, surface dynamics, and growth kinetics of group III and V metals on Si(001) are important for understanding the initial growth stage of III-V semiconductors on Si(001). Such studies can also provide valuable information for other important issues such as surfactant-mediated epitaxy, surface passivation and delta-doping layers. X-ray standing waves generated by dynamical Bragg diffraction were used as an element-specific structural probe for investigating Ga and Sb adsorption on Si(001). These high-resolution measurements reveal important quantitative structural information regarding the dimerized surface structures, and provide a stringent test for structural models proposed by various theoretical calculations. An overview of the X-ray standing wave technique and its application to surface structure and dynamics is presented.

  15. Fish retroposons related to the Penelope element of Drosophila virilis define a new group of retrotransposable elements.

    PubMed

    Volff, J N; Hornung, U; Schartl, M

    2001-06-01

    Poseidon and Neptune are two ancient lineages of retroposons related to the Penelope element from Drosophila virilis. They have been identified in various teleost fish species, including the medakafish (Oryzias latipes), and the pufferfishes Fugu rubripes and Tetraodon nigroviridis, whose genomes are currently being sequenced. Some of these elements are highly reiterated in fish genomes. Penelope-related elements were also identified in blood fluke, shrimp, sea urchin, cichlid fish and frog, showing that they are widespread in animals. Penelope-related retroposons were not detected among sequences from the Drosophila melanogaster and human genome projects, suggesting that they have been lost from certain animal lineages. A sequence encoding a putative Uri (also called GIY-YIG) endonuclease domain was detected downstream from the gene for reverse transcriptase. To the best of our knowledge, this type of endonuclease sequence has previously been identified in group I introns and in genes for prokaryotic excinucleases but not in retrotransposable elements. Penelope-related elements are frequently truncated at their 5' ends and can also be flanked by long terminal repeat-like structures. Phylogenetic analysis of the reverse transcriptase domain failed to assign Penelope-related retroposons to one of the major groups of retroelements. Overall, therefore, the evidence strongly suggests that these sequences represent a new group of retrotransposable elements.

  16. Status of |V{sub cb}| and |V{sub ub}| CKM matrix elements

    SciTech Connect

    Ricciardi, Giulia

    2016-01-22

    We summarize the status of |V{sub cb}| and |V{sub ub}| determinations, including the long standing tension among exclusive and inclusive determinations. We also discuss B meson semi-leptonic decays to excited states of the charm meson spectrum and leptonic and semileptonic B decays into final states which include τ leptons.

  17. On silicon group elements ejected by supernovae type IA

    SciTech Connect

    De, Soma; Timmes, F. X.; Brown, Edward F.; Calder, Alan C.; Townsley, Dean M.; Athanassiadou, Themis; Chamulak, David A.; Hawley, Wendy; Jack, Dennis

    2014-06-01

    There is evidence that the peak brightness of a Type Ia supernova is affected by the electron fraction Y {sub e} at the time of the explosion. The electron fraction is set by the aboriginal composition of the white dwarf and the reactions that occur during the pre-explosive convective burning. To date, determining the makeup of the white dwarf progenitor has relied on indirect proxies, such as the average metallicity of the host stellar population. In this paper, we present analytical calculations supporting the idea that the electron fraction of the progenitor systematically influences the nucleosynthesis of silicon group ejecta in Type Ia supernovae. In particular, we suggest the abundances generated in quasi-nuclear statistical equilibrium are preserved during the subsequent freeze-out. This allows potential recovery of Y {sub e} at explosion from the abundances recovered from an observed spectra. We show that measurement of {sup 28}Si, {sup 32}S, {sup 40}Ca, and {sup 54}Fe abundances can be used to construct Y {sub e} in the silicon-rich regions of the supernovae. If these four abundances are determined exactly, they are sufficient to recover Y {sub e} to 6%. This is because these isotopes dominate the composition of silicon-rich material and iron-rich material in quasi-nuclear statistical equilibrium. Analytical analysis shows the {sup 28}Si abundance is insensitive to Y {sub e}, the {sup 32}S abundance has a nearly linear trend with Y {sub e}, and the {sup 40}Ca abundance has a nearly quadratic trend with Y {sub e}. We verify these trends with post-processing of one-dimensional models and show that these trends are reflected in the model's synthetic spectra.

  18. Conserved Structural Elements in the V3 Crown of HIV-1 gp120

    SciTech Connect

    Jiang, X.; Burke, V; Totrov, M; Williams, C; Cardozo, T; Gorny, M; Zolla-Pazner, S; Kong, X

    2010-01-01

    Binding of the third variable region (V3) of the HIV-1 envelope glycoprotein gp120 to the cell-surface coreceptors CCR5 or CXCR4 during viral entry suggests that there are conserved structural elements in this sequence-variable region. These conserved elements could serve as epitopes to be targeted by a vaccine against HIV-1. Here we perform a systematic structural analysis of representative human anti-V3 monoclonal antibodies in complex with V3 peptides, revealing that the crown of V3 has four conserved structural elements: an arch, a band, a hydrophobic core and the peptide backbone. These are either unaffected by or are subject to minimal sequence variation. As these regions are targeted by cross-clade neutralizing human antibodies, they provide a blueprint for the design of vaccine immunogens that could elicit broadly cross-reactive protective antibodies.

  19. Modification of radiobiological effects of 171 MeV protons by elements of physical protection

    NASA Astrophysics Data System (ADS)

    Bulinina, Taisia; Shurshakov, Vyacheslav; Ivanov, Alexander; Molokanov, Alexander

    2016-07-01

    Space radiation includes protons of various energies. Physical protection is effective in the case of low energy protons (50-100 MeV) and becomes insufficient for radiation with a high part of high-energy protons. In the experiment performed on outbred mice, the purpose of the study was to evaluate the radiobiological effect of 171 MeV protons and protons modified by elements of physical protection of the spacecraft, on a complex of indicators of the functional condition of the system hematopoiesis and the central nervous system in 24 hours after irradiation at 20 cGy dose. The spacecraft radiation protection elements used in the experiment were a construction of wet hygiene wipes called a «protective curtain», and a glass plate imitating an ISS window. Mass thickness of the " protective curtain" in terms of water equivalent was ̴ 6,2 g/cm2. Physical shielding along the path of 171 MeV protons increases their linear energy transfer leading to the absorbed dose elevation and strengthening of the radiobiological effect. In the experiment, the two types of shielding together raised the absorbed dose from 20 to 23.2 cGy. Chemically different materials (glass and water in the wipes) were found to exert unequal modifying effects on physical and biological parameters of the proton-irradiated mice. There was a distinct dose-dependent reduction of bone marrow cellularity within the dose range from 20 cGy to 23.2 cGy in 24 hours after exposure. No modifying effect of the radiation protection elements on spontaneous motor activity was discovered when compared with entrance protons. The group of animals protected by the glass plate exhibited normal orientative-trying reactions and weakened grip with the forelimbs. The effects observed in the experiment indicate the necessity to carry out comprehensive radiobiological researches (physical, biological and mathematical) in assessing the effects of physical protection, that are actual for ensuring radiation safety of crews in

  20. The conflicting role of buckled structure in phonon transport of 2D group-IV and group-V materials.

    PubMed

    Peng, Bo; Zhang, Dequan; Zhang, Hao; Shao, Hezhu; Ni, Gang; Zhu, Yongyuan; Zhu, Heyuan

    2017-03-20

    Controlling heat transport through material design is one important step toward thermal management in 2D materials. To control heat transport, a comprehensive understanding of how structure influences heat transport is required. It has been argued that a buckled structure is able to suppress heat transport by increasing the flexural phonon scattering. Using a first principles approach, we calculate the lattice thermal conductivity of 2D mono-elemental materials with a buckled structure. Somewhat counterintuitively, we find that although 2D group-V materials have a larger mass and higher buckling height than their group-IV counterparts, the calculated κ of blue phosphorene (106.6 W mK(-1)) is nearly four times higher than that of silicene (28.3 W mK(-1)), while arsenene (37.8 W mK(-1)) is more than fifteen times higher than germanene (2.4 W mK(-1)). We report for the first time that a buckled structure has three conflicting effects: (i) increasing the Debye temperature by increasing the overlap of the pz orbitals, (ii) suppressing the acoustic-optical scattering by forming an acoustic-optical gap, and (iii) increasing the flexural phonon scattering. The former two, corresponding to the harmonic phonon part, tend to enhance κ, while the last one, corresponding to the anharmonic part, suppresses it. This relationship between the buckled structure and phonon behaviour provides insight into how to control heat transport in 2D materials.

  1. Re-187 Os-187 Isotopic and Highly Siderophile Element Systematics of Group IVB Irons

    NASA Technical Reports Server (NTRS)

    Honesto, J.; McDonough, W. F.; Walker, R. J.; McCoy, T. J.; Ash, R. D.

    2005-01-01

    Study of the magmatic iron meteorite groups permits constraints to be placed on the chemical and isotopic composition of parent bodies, and the timing of, and crystal-liquid fractionation processes involved in the crystallization of asteroidal cores. Here we examine Re-Os isotopic and trace elemental systematics of group IVB irons. Compared to most irons, the irons comprising this group are enriched in some of the most refractory siderophile elements, yet highly-depleted in most volatile siderophile elements. These characteristics have been attributed to processes such as high temperature condensation of precursor materials and oxidation in the parent body. Most recently it has been suggested that both processes may be involved in the chemical complexity of the group. Here, high precision isotopic and highly siderophile element (HSE) concentrations are used to further examine these possible origins, and the crystallization history of the group. In addition, we have begun to assess the possibility of relating certain ungrouped irons with major groups via multi-element, trace element modeling. In a companion abstract, the isotopic and trace element systematics of the ungrouped iron Tishomingo are compared with the IVB irons.

  2. Dynamic finite element analysis of third size charpy specimens of V-4Cr-4Ti

    SciTech Connect

    Lansberry, M.R.; Kumar, A.S.; Mueller, G.E.; Kurtz, R.J.

    1997-04-01

    A 2-D finite element analysis was performed on precracked, one third scale CVN specimens to investigate the sensitivity of model results to key material parameters such as yield strength, failure strain and work hardening characteristics. Calculations were carried out at temperatures of -196{degree}C and 50{degree}C. The dynamic finite element analyses were conducted using ABAQUS/Explicit V5.4. The finite element results were compared to experimental results for the production-scale heat of V-4Cr-4Ti (ANL Heat No. 832665) as a benchmark. Agreement between the finite element model and experimental data was very good at -196{degree}C, whereas at 50{degree}C the model predicted a slightly lower absorbed energy than actually measured.

  3. Relativistic Effects and the Chemistry of the Heaviest Main-Group Elements

    ERIC Educational Resources Information Center

    Thayer, John S.

    2005-01-01

    The chemical properties of the heaviest main-group elements often show features not found in their lighter counterparts while relativistic effects play an important role in the chemistry of these elements. The unusual properties and their relation to relativistic effects with emphasis on the new research are emphasized.

  4. Role of group V exchange on the shape and size of InAs/InP self-assembled nanostructures

    NASA Astrophysics Data System (ADS)

    Gutiérrez, H. R.; Cotta, M. A.; Bortoleto, J. R. R.; de Carvalho, M. M. G.

    2002-12-01

    We have studied the influence of Group V overpressure on the final shape and size of InAs nanostructures grown on (001) InP substrates. The mechanisms leading to postgrowth modifications in the InAs nanostructures are discussed. The simultaneous action of Group V overpressure and stress field—produced by the InAs nanostructures—can induce strong material transport. The direction of this material net current depends on the type of Group V element used for the overpressure flux. In situ reflection high-energy electron diffraction, atomic force microscopy, and transmission electron microscopy measurements were used to characterize the transitions in morphology. Our results show that morphological studies considering the grown surface that do not take into account postgrowth processes can be misleading to understand the growth mechanisms governing the self-assembling process.

  5. Studies of Ultra-Heavy Elements in Solar Energetic Particles Above 10 MeV/nucleon

    NASA Astrophysics Data System (ADS)

    Leske, R. A.; Cohen, C. M.; Cummings, A. C.; Mewaldt, R. A.; Stone, E. C.; Wiedenbeck, M. E.; von Rosenvinge, T. T.

    2006-05-01

    Measurements below several MeV/nucleon show that abundances of elements heavier than Ni (Z=28) can be enhanced relative to oxygen by factors of ~100 to 1000 (depending on species) in impulsive solar energetic particle (SEP) events, and large gradual events are often iron-rich and may contain admixtures of flare seed material. Recently, using the Solar Isotope Spectrometer (SIS) on NASA's ACE spacecraft, which measures the composition of energetic nuclei for elements up to ~Zr (Z=40) at energies from ~10 to >100 MeV/nucleon, we have reported detection of enhanced ultra-heavy (UH) abundances in SEP events above 10 MeV/nucleon, with resolved UH elements such as Zn, Ge and Se (Z=30, 32, and 34). We present further SIS observations of ultra-heavy SEPs that can be used to test models of acceleration and abundance enhancements in both gradual and impulsive events. By surveying the entire >8 years of ACE data, we determine the average SEP composition for elements from Z=30 to 40 and examine the time distribution of these nuclei to assess whether they arrived preferentially during gradual or impulsive events. We test whether iron-rich gradual events show noticeably larger UH enhancements than other gradual events (as expected if iron-rich events contain flare seed material), and we report cases of large excesses of UH elements in impulsive events. For example, at energies >10 MeV/nucleon, the event of 23 July 2004 had a (34

  6. Distribution of platinum group elements and other traffic related elements among different plants along some highways in Germany.

    PubMed

    Djingova, Rumiana; Kovacheva, Petya; Wagner, Gerhard; Markert, Bernd

    2003-06-01

    Using ICP-MS and ICP-AES platinum group elements (Pt, Pd, Rh, Ru and Ir) and Ce, La, Nd, Pb and Zr have been determined in street dust, Taraxacum officinale (dandelion), Plantago lanceolata (plantain), Lolium multiflorum (annual ryegrass), Rhytidiadelphus squarrosus (moss) and Vascellum pratense (mushrooms) collected along highways and streets in Germany during 1999. Among the plants Taraxacum officinale (dandelion) reflects most adequately the pollution with the investigated elements matching the results from street dust. A strong positive correlation between all elements determined in the plants is established. Transfer factor for Pt between soil and plants has been determined in an agricultural experiment ranging between 0.004 and 0.008 for two types of soils.

  7. Mono- and polynucleation, atomistic growth, and crystal phase of III-V nanowires under varying group V flow

    SciTech Connect

    Dubrovskii, V. G.

    2015-05-28

    We present a refined model for the vapor-liquid-solid growth and crystal structure of Au-catalyzed III-V nanowires, which revisits several assumptions used so far and is capable of describing the transition from mononuclear to polynuclear regime and ultimately to regular atomistic growth. We construct the crystal phase diagrams and calculate the wurtzite percentages, elongation rates, critical sizes, and polynucleation thresholds of Au-catalyzed GaAs nanowires depending on the As flow. We find a non-monotonic dependence of the crystal phase on the group V flow, with the zincblende structure being preferred at low and high group V flows and the wurtzite structure forming at intermediate group V flows. This correlates with most of the available experimental data. Finally, we discuss the atomistic growth picture which yields zincblende crystal structure and should be very advantageous for fabrication of ternary III-V nanowires with well-controlled composition and heterointerfaces.

  8. Measuring the CKM matrix element V{sub tb} at D-zero and CDF

    SciTech Connect

    Heinson, A.P.

    1997-07-01

    I present measurements by the CDF collaboration of the Standard Model three generation CKM matrix element V{sub tb} and of a special case extension with additional assumptions, using current Tevatron t{anti t} data. I then show how we can significantly improve the precision on V{sub tb} and at the same time extend the measurement so it is not constrained by Standard Model assumptions, using single top production at the upgraded Tevatron.

  9. Exploring Cryogenic Focused Ion Beam Milling as a Group III-V Device Fabrication Tool

    DTIC Science & Technology

    2013-09-01

    focused ion beam (cryo-FIB) milling as a Group III-V device fabrication tool. Cryogenic cooling of III-V semiconductor material during Ga + FIB irradiation...potential applications of cryogenic focused ion beam (cryo-FIB) milling as a Group III-V device fabrication tool. Cryogenic cooling of III-V semiconductor...sensitivity to the Ga ion beam . This sensitivity is manifested as changes in the structure and chemical composition of the starting material upon exposure to

  10. Concentrations of platinum group elements in 122 U.S. coal samples

    USGS Publications Warehouse

    Oman, C.L.; Finkelman, R.B.; Tewalt, S.J.

    1997-01-01

    Analysis of more than 13,000 coal samples by semi-quantitative optical emission spectroscopy (OES) indicates that concentrations of the platinum group elements (iridium, palladium, platinum, osmium, rhodium, and ruthenium) are less than 1 ppm in the ash, the limit of detection for this method of analysis. In order to accurately determine the concentration of the platinum group elements (PGE) in coal, additional data were obtained by inductively coupled plasma mass spectroscopy, an analytical method having part-per-billion (ppb) detection limits for these elements. These data indicate that the PGE in coal occur in concentrations on the order of 1 ppb or less.

  11. Trace element bioaccumulation in reef fish from New Caledonia: influence of trophic groups and risk assessment for consumers.

    PubMed

    Metian, Marc; Warnau, Michel; Chouvelon, Tiphaine; Pedraza, Fernando; Rodriguez y Baena, Alessia M; Bustamante, Paco

    2013-01-01

    Fourteen trace elements (Ag, As, Cd, Co, Cr, Cu, Fe, Hg, Mn, Ni, Pb, Se, V, and Zn) were analyzed in livers and muscles from 22 fish species from the New Caledonia lagoon, which is subjected to important chemical inputs due to intense land-based mining activities (New Caledonia is the third largest world producer of Ni). The results of this baseline research indicated that livers generally concentrated trace elements to a greater extent than muscles. Nevertheless, the overall trace element concentrations in both tissues were barely above the levels reported in fish and thus contamination at the local scale was poorly discriminated. Although these levels were low, preliminary risk assessment from a global health standpoint suggests that As would be an element potentially leading to exposure of concern for fish consumers. Based on the trace element concentrations in livers and the fish trophic preferences, some trends have been observed among trophic groups: Ag, Cu, Fe, Hg, and Zn concentrations were generally higher in liver of fish with the highest trophic position whereas Cd concentrations were lower in these groups. The use of the leopard coral grouper Plectropomus leopardus as a resident top predator allowed determining the geographical variations in contamination levels with significant differences for six out of the fourteen elements investigated. The sampling sites influenced by anthropogenic inputs were revealed by high Ag, Cd, Cu, Hg, and Pb concentrations. Such geographic differences also applied to Zn but surprisingly not for the typical elements associated with Ni mining, i.e., Co, Cr, Mn and Ni.

  12. Voltage-dependent sodium (NaV) channels in group IV sensory afferents

    PubMed Central

    Elmslie, Keith S

    2016-01-01

    Patients with intermittent claudication suffer from both muscle pain and an exacerbated exercise pressor reflex. Excitability of the group III and group IV afferent fibers mediating these functions is controlled in part by voltage-dependent sodium (NaV) channels. We previously found tetrodotoxin-resistant NaV1.8 channels to be the primary type in muscle afferent somata. However, action potentials in group III and IV afferent axons are blocked by TTX, supporting a minimal role of NaV1.8 channels. To address these apparent differences in NaV channel expression between axon and soma, we used immunohistochemistry to identify the NaV channels expressed in group IV axons within the gastrocnemius muscle and the dorsal root ganglia sections. Positive labeling by an antibody against the neurofilament protein peripherin was used to identify group IV neurons and axons. We show that >67% of group IV fibers express NaV1.8, NaV1.6, or NaV1.7. Interestingly, expression of NaV1.8 channels in group IV somata was significantly higher than in the fibers, whereas there were no significant differences for either NaV1.6 or NaV1.7. When combined with previous work, our results suggest that NaV1.8 channels are expressed in most group IV axons, but that, under normal conditions, NaV1.6 and/or NaV1.7 play a more important role in action potential generation to signal muscle pain and the exercise pressor reflex. PMID:27385723

  13. The bcr1 DNA Repeat Element Is Specific to the Bacillus cereus Group and Exhibits Mobile Element Characteristics

    PubMed Central

    Økstad, Ole Andreas; Tourasse, Nicolas J.; Stabell, Fredrik B.; Sundfær, Cathrine K.; Egge-Jacobsen, Wolfgang; Risøen, Per Arne; Read, Timothy D.; Kolstø, Anne-Brit

    2004-01-01

    Bacillus cereus strains ATCC 10987 and ATCC 14579 harbor a ∼155-bp repeated element, bcr1, which is conserved in B. cereus, B. anthracis, B. thuringiensis, and B. mycoides but not in B. subtilis and B. licheniformis. In this study, we show by Southern blot hybridizations that bcr1 is present in all 54 B. cereus group strains tested but absent in 11 Bacillus strains outside the group, suggesting that bcr1 may be specific and ubiquitous to the B. cereus group. By comparative analysis of the complete genome sequences of B. cereus ATCC 10987, B. cereus ATCC 14579, and B. anthracis Ames, we show that bcr1 is exclusively present in the chromosome but absent from large plasmids carried by these strains and that the numbers of full-length bcr1 repeats for these strains are 79, 54, and 12, respectively. Numerous copies of partial bcr1 elements are also present in the three genomes (91, 128, and 53, respectively). Furthermore, the genomic localization of bcr1 is not conserved between strains with respect to chromosomal position or organization of gene neighbors, as only six full-length bcr1 loci are common to at least two of the three strains. However, the intergenic sequence surrounding a specific bcr1 repeat in one of the three strains is generally strongly conserved in the other two, even in loci where bcr1 is found exclusively in one strain. This finding indicates that bcr1 either has evolved by differential deletion from a very high number of repeats in a common ancestor to the B. cereus group or is moving around the chromosome. The identification of bcr1 repeats interrupting genes in B. cereus ATCC 10987 and ATCC 14579 and the presence of a flanking TTTAT motif in each end show that bcr1 exhibits features characteristic of a mobile element. PMID:15516586

  14. The Abundances of the Fe Group Elements in Early B Stars in the Magellanic Clouds and Our Galaxy

    NASA Astrophysics Data System (ADS)

    Peters, Geraldine Joan; Adelman, Saul Joseph

    2015-08-01

    The abundances of the Fe-peak elements (Ti, V, Cr, Mn, Fe, Co, and Ni) are of interest as they are important for assessing opacities for stellar evolution calculations, confirming theoretical calculations of explosive nucleosynthesis, and inferring the past history of supernova activity in a galaxy. FUSE FUV spectra of early B stars in the LMC and SMC and HST/STIS FUV/NUV spectra of nearby B stars in our galaxy are analyzed with the Hubeny/Lanz programs TLUSTY/SYNSPEC to determine abundance for the Fe group elements and produce a map of these abundances in the Magellanic Clouds (MC) and Magellanic Bridge (MB). Except for four weak multiplets of Fe III there are no measurable lines from the Fe group in the optical region. The Fe group species found in the FUV spectra of early B stars are primarily in the second stage of ionization. The best set of lines in the FUSE spectral region are Fe III (UV1), V III 1150 Å, and Cr III 1137 Å. Analysis of the galactic B stars provides a good assessment of the reliability of the atomic parameters that are used for the MC calculations. Twenty-two early B stars in the MC and MB and five in our galaxy were analyzed. In general the Fe group abundances range from solar to slightly below solar in our region of the galaxy. But in the MCs the abundances of V, Cr, and Fe tend to be significantly lower than the mean metal abundances for the galaxy. Maps of the Fe group abundances and their variations in the LMC and SMC, tracers of recent enrichment of the ISM from supernova activity, are shown. Support from NASA grants NAG5-13212, NNX10AD66G, STScI HST-GO-13346.22, and USC’s Women in Science and Engineering (WiSE) program is greatly appreciated.

  15. sp3-hybridized framework structure of group-14 elements discovered by genetic algorithm

    SciTech Connect

    Nguyen, Manh Cuong; Zhao, Xin; Wang, Cai-Zhuang; Ho, Kai-Ming

    2014-05-01

    Group-14 elements, including C, Si, Ge, and Sn, can form various stable and metastable structures. Finding new metastable structures of group-14 elements with desirable physical properties for new technological applications has attracted a lot of interest. Using a genetic algorithm, we discovered a new low-energy metastable distorted sp3-hybridized framework structure of the group-14 elements. It has P42/mnm symmetry with 12 atoms per unit cell. The void volume of this structure is as large as 139.7Å3 for Si P42/mnm, and it can be used for gas or metal-atom encapsulation. Band-structure calculations show that P42/mnm structures of Si and Ge are semiconducting with energy band gaps close to the optimal values for optoelectronic or photovoltaic applications. With metal-atom encapsulation, the P42/mnm structure would also be a candidate for rattling-mediated superconducting or used as thermoelectric materials.

  16. The measurement of elemental abundances above 10 sup 15 eV at a lunar base

    SciTech Connect

    Swordy, S.P. )

    1990-03-15

    At {approx}10{sup 15} eV the slope of the energy spectrum of cosmic rays becomes significantly steeper than at lower energies. The measurement of relative elemental abundances at these energies is expected to provide a means to resolve the origin of this feature and greatly contribute to the understanding of the sources of cosmic rays. We describe a moon based detector for making well resolved elemental measurements at these energies using hadronic calorimetry. This detector is particularly well suited for a site on the lunar surface because there is no overlying layer of atmosphere and the large mass required can be provided by the lunar regolith.

  17. 25 years of N-heterocyclic carbenes: activation of both main-group element-element bonds and NHCs themselves.

    PubMed

    Würtemberger-Pietsch, Sabrina; Radius, Udo; Marder, Todd B

    2016-04-14

    N-Heterocyclic carbenes (NHCs) are widely used ligands and reagents in modern inorganic synthesis as well as in homogeneous catalysis and organocatalysis. However, NHCs are not always innocent bystanders. In the last few years, more and more examples were reported of reactions of NHCs with main-group elements which resulted in modification of the NHC. Many of these reactions lead to ring expansion and the formation of six-membered heterocyclic rings involving insertion of the heteroatom into the C-N bond and migration of hydrides, phenyl groups or boron-containing fragments. Furthermore, a few related NHC rearrangements were observed some decades ago. In this Perspective, we summarise the history of NHC ring expansion reactions from the 1960s till the present.

  18. V1/V2 Neutralizing Epitope is Conserved in Divergent Non-M Groups of HIV-1

    PubMed Central

    Morgand, Marion; Bouvin-Pley, Mélanie; Plantier, Jean-Christophe; Moreau, Alain; Alessandri, Elodie; Simon, François; Pace, Craig S.; Pancera, Marie; Ho, David D.; Poignard, Pascal; Bjorkman, Pamela J.; Mouquet, Hugo; Nussenzweig, Michel C.; Kwong, Peter D.; Baty, Daniel; Chames, Patrick; Braibant, Martine

    2016-01-01

    Background: Highly potent broadly neutralizing monoclonal antibodies (bNAbs) have been obtained from individuals infected by HIV-1 group M variants. We analyzed the cross-group neutralization potency of these bNAbs toward non-M primary isolates (PI). Material and Methods: The sensitivity to neutralization was analyzed in a neutralization assay using TZM-bl cells. Twenty-three bNAbs were used, including reagents targeting the CD4-binding site, the N160 glycan-V1/V2 site, the N332 glycan-V3 site, the membrane proximal external region of gp41, and complex epitopes spanning both env subunits. Two bispecific antibodies that combine the inhibitory activity of an anti-CD4 with that of PG9 or PG16 bNAbs were included in the study (PG9-iMab and PG16-iMab). Results: Cross-group neutralization was observed only with the bNAbs targeting the N160 glycan-V1/V2 site. Four group O PIs, 1 group N PI, and the group P PI were neutralized by PG9 and/or PG16 or PGT145 at low concentrations (0.04–9.39 μg/mL). None of the non-M PIs was neutralized by the bNAbs targeting other regions at the highest concentration tested, except 10E8 that neutralized weakly 2 group N PIs and 35O22 that neutralized 1 group O PI. The bispecific bNAbs neutralized very efficiently all the non-M PIs with IC50 below 1 μg/mL, except 2 group O strains. Conclusion: The N160 glycan-V1/V2 site is the most conserved neutralizing site within the 4 groups of HIV-1. This makes it an interesting target for the development of HIV vaccine immunogens. The corresponding bNAbs may be useful for immunotherapeutic strategies in patients infected by non-M variants. PMID:26413851

  19. Verbesserte Elemente der RR-Lyrae-Sterne IQ Bootis, V651 Aurigae und BQ Lyrae

    NASA Astrophysics Data System (ADS)

    Maintz, Gisela

    2015-04-01

    CCD observations of neglected RR Lyrae stars were taken at my private observatory. IQ Boo is a RRab star with a hump in the rising branch. BQ Lyr shows a weak Blazhko effect. The elements of these stars were revised. Star Max period +- JD [d] [d] IQ Boo 2457213.4681 0.535234 0.000001 V651 Aur 2457040.4056 0.617715 0.000003 BQ Lyr 2455703.4120 0.4350488 0.0000002

  20. Levels of platinum group elements and rare-earth elements in wild mushroom species growing in Poland.

    PubMed

    Mleczek, Mirosław; Niedzielski, Przemysław; Kalač, Pavel; Siwulski, Marek; Rzymski, Piotr; Gąsecka, Monika

    2016-01-01

    Due to limited data-describing abilities of mushrooms to accumulate platinum group elements (PGEs) and rare-earth elements (REEs), the aim of this study was to determine, by inductively coupled plasma optical emission spectrometry followed by microwave-assisted sample digestion by nitric acid, the content of these elements in 20 mushroom species (10 above ground and 10 growing on wood), mostly edible, collected near a busy trunk road. The highest content of PGEs in above-ground mushroom species was observed in Lepista gilva and Suillus bovinus fruit bodies (0.38 ± 0.05 and 0.37 ± 0.03 mg kg(-1) DW, respectively), while in mushrooms growing on wood, the highest content was observed in Pleurotus ostreatus (0.35 ± 0.04 mg kg(-1) DW). The mean content of PGEs for both these groups was 0.23 ± 0.08 and 0.26 ± 0.07 mg kg(-1) DW, respectively. The highest content of REEs in Suillus luteus and Tricholoma equestra was 5.03 ± 0.50 and 2.18 ± 0.56 mg kg(-1) DW, respectively, but within mushrooms growing on wood in Ganoderma applanatum fruiting bodies it was 4.19 ± 0.78 mg kg(-1) DW. Mean contents of REEs were 1.39 ± 1.21 and 1.61 ± 0.97 mg kg(-1) DW in above-ground species and species growing on wood, respectively. Generally, the group of mushroom species growing on wood was capable of slightly higher accumulation of both REEs and PGEs. No limits have been established for both the groups until now.

  1. A novel upstream element compensates for an ineffectual octamer motif in an immunoglobulin V kappa promoter.

    PubMed Central

    Atchison, M L; Delmas, V; Perry, R P

    1990-01-01

    The octamer (or dc/cd) motif is considered to be a critical component of all immunoglobulin (Ig) promoters. Although the sequence of this motif is highly conserved among most Ig promoters, there are some notable examples in which efficiently expressed Ig genes contain divergent octamers with base substitutions that are demonstrably deleterious when tested with heterologous proximal promoter elements. To elucidate the mechanisms that enable these naturally occurring Ig genes to cope with divergent octamers, we analyzed two such promoters with regard to their ability to interact with relevant transcription factors. We found that the divergent octamer in the kappa O germline promoter strongly binds both Oct-1 and Oct-2 factors, presumably because of compensatory contributions by flanking DNA sequences. A more surprising result was obtained with the V kappa 19 promoter. In this case, the divergent octamer is a very weak Oct factor binding site and, without help from another upstream element, is inadequate for efficient promoter function. This additional element, termed kappa Y because of its high pyrimidine content (CTTCCTTA), serves as a binding site for a novel lymphoid-specific factor. When the divergent V kappa 19 octamer was converted to a strong Oct factor binding site by a single point mutation, the need for kappa Y was obviated. Interestingly, VH promoters that contain the same divergent octamer also contain an upstream element that is very similar to kappa Y. Images Fig. 1. Fig. 2. Fig. 3. Fig. 4. Fig. 5. Fig. 6. Fig. 7. Fig. 8. PMID:2120037

  2. Radiochemical Separation of Group 5 Elements. Model Experiments for Investigation of Dubnium Chemical Behaviour

    SciTech Connect

    Tereshatov, E. E.; Bozhikov, G. A.; Aksenov, N. V.; Starodub, G. Ya.; Vostokin, G. K.; Shishkin, S. V.; Dmitriev, S. N.; Bruchertseifer, H.; Gaeggeler, H. W.

    2007-05-22

    Chemical behaviour of group 5 elements in the aqueous hydrofluoric acid solutions was studied. The radiochemical method for the cation exchange separation of Nb (Pa) and Ta from Zr, Hf and lanthanides is presented. The developed scheme allows excluding of the presence of SF heavy actinides in fractions of separated elements. On the basis of the data of the present work, it is possible to suggest the following order of the stability of the fluoride complexes of group 4 and 5 elements: Nb {approx_equal} Pa > Zr > Hf > Ta. The order of the complex formation is in agreement with theoretical predictions. This analytical procedure can be used in future heavy nuclei synthesis experiments for the separation of dubnium (Db) from other reactions products and for its chemical identification.

  3. IMPORTANCE OF ACTIVATED CARBON'S OXYGEN SURFACE FUNCTIONAL GROUPS ON ELEMENTAL MERCURY ADSORPTION

    EPA Science Inventory

    The effect of varying physical and chemical properties of activated carbons on adsorption of elemental mercury [Hg(0)] was studied by treating two activated carbons to modify their surface functional groups and pore structures. Heat treatment (1200 K) in nitrogen (N2), air oxidat...

  4. Functional groups and elemental analyses of cuticular morphotypes of Cordaites principalis (Germar) Geinitz, Carboniferous Maritimes Basin, Canada

    USGS Publications Warehouse

    Zodrow, E.L.; Mastalerz, Maria; Orem, W.H.; Simunek, Z.; Bashforth, A.R.

    2000-01-01

    Well-preserved cuticles were isolated from Cordaites principalis (Germar) Geinitz leaf compressions, i.e., foliage from extinct gymnosperm trees Coniferophyta: Order Cordaitales. The specimens were collected from the Sydney. Stellarton and Bay St. George subbasins of the once extensive Carboniferous Maritimes Basin of Atlantic Canada. Fourier transformation of infrared spectra (FTIR) and elemental analyses indicate that the ca. 300-306-million-year-old fossil cuticles share many of the functional groups observed in modern cuticles. The similarities of the functional groups in each of the three cuticular morphotypes studied support the inclusion into a single cordaite-leaf taxon, i.e., C. principalis (Germar), confirming previous morphological investigations. Vitrinite reflectance measurements on coal seams in close proximity to the fossil-bearing sediments reveal that the Bay St. George sample site has the lowest thermal maturity, whereas the sites in Sydney and Stellarton are more mature. IR absorption and elemental analyses of the cordaite compressions corroborate this trend, which suggests that the coalified mesophyll in the leaves follows a maturation path similar to that of vitrinite. Comparison of functional groups of the cordaite cuticles with those from certain pteridosperms previously studied from the Sydney Subbasin shows that in the cordaite cuticles highly conjugated C-O (1632 cm-1) bands dominate over carbonyl stretch that characterizes the pteridosperm cuticles. The differences demonstrate the potential of chemotaxonomy as a valuable tool to assist distinguishing between Carboniferous plant-fossil groups. Published by Elsevier Science B.V.

  5. Group 14 hydrides with low valent elements for activation of small molecules.

    PubMed

    Mandal, Swadhin K; Roesky, Herbert W

    2012-02-21

    Transition metal compounds are well known as activators of small molecules, and they serve as efficient catalysts for a variety of homogeneous and heterogeneous transformations. In contrast, there is a general feeling that main group compounds cannot act as efficient catalysts because of their inability to activate small molecules. Traditionally, the activation of small molecules is considered one of the key steps during a catalytic cycle with transition metals. As a consequence, researchers have long neglected the full range of possibilities in harnessing main group elements for the design of efficient catalysts. Recent developments, however, have made it possible to synthesize main group compounds with low-valent elements capable of activating small molecules. In particular, the judicious use of sterically appropriate ligands has been successful in preparing and stabilizing a variety of Group 14 hydrides with low-valent elements. In this Account, we discuss recent advances in the synthesis of Group 14 hydrides with low-valent elements and assess their potential as small-molecule activators. Group 14, which comprises the nonmetal C, the semimetals Si and Ge, and the metals Sn and Pb, was for years a source of hydrides with the Group 14 element almost exclusively in tetravalent form. Synthetic difficulties and the low stability of Group 14 hydrides in lower oxidation states were difficult to overcome. But in 2000, a divalent Sn(II) hydride was prepared as a stable compound through the incorporation of sterically encumbered aromatic ligands. More recently, the stabilization of GeH(2) and SnH(2) complexes using an N-heterocyclic carbene (NHC) as a donor and BH(3) or a metal carbonyl complex as an acceptor was reported. A similar strategy was also employed to synthesize the Si(II) hydride. This class of hydrides may be considered coordinatively saturated, with the lone pair of electrons on the Group 14 elements taking part in coordination. We discuss the large

  6. Source characterisation of atmospheric platinum group element deposition into an ombrotrophic peat bog.

    PubMed

    Rauch, Sebastien; Hemond, Harold F; Peucker-Ehrenbrink, Bernhard

    2004-04-01

    Platinum, palladium, rhodium, iridium and osmium were found to be enriched relative to their expected natural concentrations in peat samples from Thoreau's Bog, an ombrotrophic peat bog in Concord, Massachusetts. The source of osmium into the bog was determined from its isotopic composition (187Os/188Os). Osmium is composed of 4% lithogenic osmium from atmospheric soil dust, 41% of anthropogenic osmium and 55% of osmium from a non-lithogenic, non anthropogenic source, with rain being a likely candidate for the latter. Significant anthropogenic and rain contributions are also expected for iridium. In contrast, platinum, palladium and rhodium are almost exclusively anthropogenic. The larger enrichments of platinum, palladium and rhodium indicate that automobile catalysts are the source of platinum group elements to Thoreau's bog. The bog is located approximately 300 m from a major road and, therefore, the occurrence of platinum elements is evidence for regional dispersion of these metals. The absence of a clear trend following the introduction of catalysts indicates that platinum group elements are not quantitatively conserved in peat with downward leaching and plants playing an important role in the accumulation of platinum group elements.

  7. Impact Behavior of A356 Foundry Alloys in the Presence of Trace Elements Ni and V

    NASA Astrophysics Data System (ADS)

    Casari, Daniele; Ludwig, Thomas H.; Merlin, Mattia; Arnberg, Lars; Garagnani, Gian Luca

    2015-02-01

    In the present work, the impact behavior of unmodified A356 alloys with the addition of Ni or V in as-cast and T6 heat-treated conditions was assessed. Charpy V-notched specimens obtained from sand and permanent mold casting showed low total absorbed energy average values ( W t < 2 J). SEM analysis of fracture profiles and surfaces indicated a Si-driven crack propagation with a predominant transgranular fracture mode. Occasionally, intergranular contributions to fracture were detected in the permanent mold cast alloys due to the locally finer microstructure. Concurrent mechanisms related to the chemical composition, solidification conditions and heat treatment were found to control the impact properties of the alloys. While the trace element Ni exerted only minor effects on the impact toughness of the A356 alloy, V had a strong influence: (i) V-containing sand cast alloys absorbed slightly higher impact energies compared to the corresponding A356 base alloys; (ii) in the permanent mold cast alloys, V in solid solution led to a considerable loss of ductility, which in turn decreased the total absorbed energy.

  8. Adhesion and friction behavior of group 4 elements germanium, silicon, tin, and lead

    NASA Technical Reports Server (NTRS)

    Buckley, D. H.

    1975-01-01

    Adhesion and friction studies were conducted with thin films of the group IV elements silicon, germanium, tin, and lead ion plated on the nickel (011) substrate. The mating surface was gold (111). Contacts were made for the elements in the clean state and with oxygen present. Adhesion and friction experiments were conducted at very light loads of 1 to 10 g. Sliding was at a speed of 0.7 mm/min. Friction results indicate that the more covalently bonded elements silicon and germanium exhibit lower adhesion and friction than the more metallic bonded tin and lead. The adhesion of gold to germanium was observed, and recrystallization of the transferred gold occurred. Plastic flow of germanium was seen with sliding. Oxygen reduced, but did not eliminate, the adhesion observed with germanium and silicon.

  9. Implementation of Hybrid V-Cycle Multilevel Methods for Mixed Finite Element Systems with Penalty

    NASA Technical Reports Server (NTRS)

    Lai, Chen-Yao G.

    1996-01-01

    The goal of this paper is the implementation of hybrid V-cycle hierarchical multilevel methods for the indefinite discrete systems which arise when a mixed finite element approximation is used to solve elliptic boundary value problems. By introducing a penalty parameter, the perturbed indefinite system can be reduced to a symmetric positive definite system containing the small penalty parameter for the velocity unknown alone. We stabilize the hierarchical spatial decomposition approach proposed by Cai, Goldstein, and Pasciak for the reduced system. We demonstrate that the relative condition number of the preconditioner is bounded uniformly with respect to the penalty parameter, the number of levels and possible jumps of the coefficients as long as they occur only across the edges of the coarsest elements.

  10. Four-group stabilized zoom lens design of two focal-length-variable elements.

    PubMed

    Hao, Qun; Cheng, Xuemin; Du, Ke

    2013-03-25

    We present a theoretical method for analyzing the first-order optics of stabilized zoom lenses with two focal-length-variable elements. The zoom equations are established through the use of the Gaussian brackets method. This is done because the optical power of the focal-length-variable elements varies during the zooming process. The first and second derivatives and the Hessian matrix of the zoom equations with respect to the Gaussian parameters are determined using the equations. These parameters could represent the sensitivity of the zoom ratio of the system to changes in the corresponding system variables. We select the initial values of these system variables, i.e. the magnification of the focal-length-variable element and the structure parameters of the fixed lens group, to be close to the steepest gradient direction. Here the sensitivity of the system focal length is high with respect to variations in the zoom variables. This process leads to an increase in the zoom ratio of the zoom system. The results show successful four-group stabilized zoom lens designs with 2:1 and 5:1 zoom ratios, using two deformable mirrors as focal-length-variable elements. This system, with the inherent characteristics of a steepest gradient, could miniaturize zoom systems.

  11. Theoretical discovery of stable structures of group III-V monolayers: The materials for semiconductor devices

    SciTech Connect

    Suzuki, Tatsuo

    2015-11-23

    Group III-V compounds are very important as the materials of semiconductor devices. Stable structures of the monolayers of group III-V binary compounds have been discovered by using first-principles calculations. The primitive unit cell of the discovered structures is a rectangle, which includes four group-III atoms and four group-V atoms. A group-III atom and its three nearest-neighbor group-V atoms are placed on the same plane; however, these connections are not the sp{sup 2} hybridization. The bond angles around the group-V atoms are less than the bond angle of sp{sup 3} hybridization. The discovered structure of GaP is an indirect transition semiconductor, while the discovered structures of GaAs, InP, and InAs are direct transition semiconductors. Therefore, the discovered structures of these compounds have the potential of the materials for semiconductor devices, for example, water splitting photocatalysts. The discovered structures may become the most stable structures of monolayers which consist of other materials.

  12. Influence of main-group element on half-metallic properties in half-Heusler compound

    NASA Astrophysics Data System (ADS)

    Liu, Hongyan; Li, Yushan; Tian, Fuyang; Li, Getian

    2016-04-01

    We investigate the band structure, magnetism and density of states of half-Heusler compounds CoCrZ (Z = Si,Ge,P,As) based on the first-principle calculations. Combined with molecular orbital hybridization theory, we discuss the influence of the main-group element on half-metallic properties of CoCrZ. It is found that the replacement of Ge for Si in CoCrSi can adjust the position of the Fermi level, and while it has no impact on the energy gap width and magnetic structure. However, the substitution of P for Si can effectively adjust the magnetism without disrupting its half-metallicity. Our results demonstrate that the electronic structure of CoCrZ is mainly dependent on the number of valence electrons of the main-group element.

  13. Minority carrier device comprising a passivating layer including a Group 13 element and a chalcogenide component

    NASA Technical Reports Server (NTRS)

    Barron, Andrew R. (Inventor); Hepp, Aloysius F. (Inventor); Jenkins, Phillip P. (Inventor); MacInnes, Andrew N. (Inventor)

    1999-01-01

    A minority carrier device includes at least one junction of at least two dissimilar materials, at least one of which is a semiconductor, and a passivating layer on at least one surface of the device. The passivating layer includes a Group 13 element and a chalcogenide component. Embodiments of the minority carrier device include, for example, laser diodes, light emitting diodes, heterojunction bipolar transistors, and solar cells.

  14. Vertical group III-V nanowires on si, heterostructures, flexible arrays and fabrication

    DOEpatents

    Wang, Deli; Soci, Cesare; Bao, Xinyu; Wei, Wei; Jing, Yi; Sun, Ke

    2015-01-13

    Embodiments of the invention provide a method for direct heteroepitaxial growth of vertical III-V semiconductor nanowires on a silicon substrate. The silicon substrate is etched to substantially completely remove native oxide. It is promptly placed in a reaction chamber. The substrate is heated and maintained at a growth temperature. Group III-V precursors are flowed for a growth time. Preferred embodiment vertical Group III-V nanowires on silicon have a core-shell structure, which provides a radial homojunction or heterojunction. A doped nanowire core is surrounded by a shell with complementary doping. Such can provide high optical absorption due to the long optical path in the axial direction of the vertical nanowires, while reducing considerably the distance over which carriers must diffuse before being collected in the radial direction. Alloy composition can also be varied. Radial and axial homojunctions and heterojunctions can be realized. Embodiments provide for flexible Group III-V nanowire structures. An array of Group III-V nanowire structures is embedded in polymer. A fabrication method forms the vertical nanowires on a substrate, e.g., a silicon substrate. Preferably, the nanowires are formed by the preferred methods for fabrication of Group III-V nanowires on silicon. Devices can be formed with core/shell and core/multi-shell nanowires and the devices are released from the substrate upon which the nanowires were formed to create a flexible structure that includes an array of vertical nanowires embedded in polymer.

  15. Advances in the development of complexes that contain a group 13 element chalcogen multiple bond.

    PubMed

    Franz, Daniel; Inoue, Shigeyoshi

    2016-06-21

    Inorganic group 13 element (M) chalcogenides (E) based on the general formular M2E3 are ubiquitous in synthesis, catalysis and material science. The parent ME fragment which aggregates to form three dimensional networks in the condensed phase can be expected to exhibit multiple bond character between the elements. Low temperature matrix isolation techniques are required to investigate the nature of this elusive species. An alternate approach for respective studies is the synthesis of electron-precise molecular complexes that contain the ME entity and for which isolation at ambient temperature is possible. This is realized by kinetic stabilization with bulky ligands and thermodynamic stabilization using electron donor, as well as acceptor groups attached to the ME functionality (i.e. donor-acceptor stabilization). In this article we revise the literature on complex compounds that exhibit a bonding interaction between a group 13 element atom and a chalcogen atom that is reasonably to be interpreted in terms of a double- or triple bond.

  16. 77 FR 43071 - MPS Customer Group v. Maine Public Service Company; Notice of Complaint

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-07-23

    ... Energy Regulatory Commission MPS Customer Group v. Maine Public Service Company; Notice of Complaint Take... Commission (Commission); 18 CFR 385.206, MPS Customer Group (Complainant) filed a formal complaint against... Complainant certifies that copies of the complaint were served on the contacts for the Respondent. Any...

  17. Cytogenetic mapping of the Muller F element genes in Drosophila willistoni group.

    PubMed

    Pita, Sebastián; Panzera, Yanina; Lúcia da Silva Valente, Vera; de Melo, Zilpa das Graças Silva; Garcia, Carolina; Garcia, Ana Cristina Lauer; Montes, Martín Alejandro; Rohde, Claudia

    2014-10-01

    Comparative genomics in Drosophila began in 1940, when Muller stated that the ancestral haploid karyotype of this genus is constituted by five acrocentric chromosomes and one dot chromosome, named A to F elements. In some species of the willistoni group such as Drosophila willistoni and D. insularis, the F element, instead of a dot chromosome, has been incorporated into the E element, forming chromosome III (E + F fusion). The aim of this study was to investigate the scope of the E + F fusion in the willistoni group, evaluating six other species. Fluorescent in situ hybridization was used to locate two genes of the F element previously studied-cubitus interruptus (ci) and eyeless (ey)-in species of the willistoni and bocainensis subgroups. Moreover, polytene chromosome photomaps corresponding to the F element (basal portion of chromosome III) were constructed for each species studied. In D. willistoni, D. paulistorum and D. equinoxialis, the ci gene was located in subSectction 78B and the ey gene in 78C. In D. tropicalis, ci was located in subSection 76B and ey in 76C. In species of the bocainensis subgroup, ci and ey were localized, respectively, at subsections 76B and 76C in D. nebulosa and D. capricorni, and 76A and 76C in D. fumipennis. Despite the differences in the subsection numbers, all species showed the same position for ci and ey. The results confirm the synteny of E + F fusion in willistoni and bocainensis subgroups, and allow estimating the occurrence of this event at 15 Mya, at least.

  18. Synthetic multilayer x-ray dispersion elements for 200 A (62 eV) to 0. 62 A (20 keV) radiation. Final report

    SciTech Connect

    Barbee, T.W. Jr.

    1983-11-01

    This final report concerns research performed at Stanford University on a program sponsored by the Department of Energy through Lawrence Livermore National Laboratory and the Regents of the University of California (Subcontract No. 2695501) entitled Synthetic Multilayer X-ray Dispersion Elements for 200 A (62 eV) to 0.62 A (20 keV) Radiation. The thrust of the research was to investigate the synthesis process parameter dependence of the nature of the interfaces between constituent adjacent layers, the uniformity of layers, and the reflectivity for light of wavelengths 0.62 A to 200 A of synthetic multilayer crystals. Additionally, device development was to be undertaken with emphasis on spectrum analyzing dispersion elements, high energy Kirkpatrick-Baez X-ray microscope mirrors, multi-keV (1 to 5 keV) X-ray applications, X-ray beam splitters and synthetic multilayers fabricated from adjoining elements in the periodic table.

  19. Partitioning of Si and platinum group elements between liquid and solid Fe-Si alloys

    NASA Astrophysics Data System (ADS)

    Morard, G.; Siebert, J.; Badro, J.

    2014-05-01

    Crystallization of the Earth's inner core fractionates major and minor elements between the solid and liquid metal, leaving physical and geochemical imprints on the Earth's core. For example, the density jump observed at the Inner Core Boundary (ICB) is related to the preferential partitioning of lighter elements in the liquid outer core. The fractionation of Os, Re and Pt between liquid and solid during inner core crystallization has been invoked as a process that explains the observed Os isotopic signature of mantle plume-derived lavas (Brandon et al., 1998; Brandon and Walker, 2005) in terms of core-mantle interaction. In this article we measured partitioning of Si, Os, Re and Pt between liquid and solid metal. Isobaric (2 GPa) experiments were conducted in a piston-cylinder press at temperatures between 1250 °C and 1600 °C in which an imposed thermal gradient through the sample provided solid-liquid coexistence in the Fe-Si system. We determined the narrow melting loop in the Fe-Si system using Si partitioning values and showed that order-disorder transition in the Fe-Si solid phases can have a large effect on Si partitioning. We also found constant partition coefficients (DOs, DPt, DRe) between liquid and solid metal, for Si concentrations ranging from 2 to 12 wt%. The compact structure of Fe-Si liquid alloys is compatible with incorporation of Si and platinum group elements (PGEs) elements precluding solid-liquid fractionation. Such phase diagram properties are relevant for other light elements such as S and C at high pressure and is not consistent with inter-elemental fractionation of PGEs during metal crystallization at Earth's inner core conditions. We therefore propose that the peculiar Os isotopic signature observed in plume-derived lavas is more likely explained by mantle source heterogeneity (Meibom et al., 2002; Baker and Krogh Jensen, 2004; Luguet et al., 2008).

  20. Stabilization of hexa-coordinated P(v) corroles by axial silyloxy groups.

    PubMed

    Chatterjee, Tamal; Lee, Way-Zen; Ravikanth, Mangalampalli

    2016-05-04

    We report the stabilization of the hexa-coordination environment for P(v) corroles by using alkyl/aryl substituted silyloxy groups as axial ligands. The P(v) corroles are highly fluorescent in a hexa-coordination environment compared to in a penta-coordination environment. However, P(v) corroles generally undergo axial ligand dissociation to form a mixture of penta- and hexa-coordinated P(v) corroles in non-coordinating solvents such as toluene, CH2Cl2, CHCl3. The usage of moderately bulkier and electron-donating silyloxy groups helps to restrict the axial ligand dissociation of silyloxy substituted hexa-coordinated P(v) corroles in non-coordinating solvents. The crystal structure confirmed the hexa-coordination geometry for the P(v) corroles. The P(v) corroles strongly absorb and emit in the visible region, with decent quantum yields and singlet state lifetimes. The hexa-coordinated P(v) corroles are highly stable under electrochemical conditions.

  1. Room temperature ferromagnetism in Ist group elements codoped ZnO:Fe nanoparticles by co-precipitation method

    NASA Astrophysics Data System (ADS)

    Pazhanivelu, V.; Paul Blessington Selvadurai, A.; Kannan, R.; Murugaraj, R.

    2016-04-01

    In this paper, we report on the structural, vibrational and magnetic behavior of Ist group elements (Li+, Na+ and K+) codoping effect in ZnO:Fe nanoparticles (NPs) prepared by co-precipitation method. The single crystalline phase of the prepared NPs was identified as Wurtizite structure and the Raman spectra expressed the local structural change and the presence of complex lattice defects such as Zinc interstitial (Zni) and Oxygen vacanvy (V+o) defects in the NPs. The presence of functional groups was confirmed by FT-IR spectral analysis. The optical absorption properties of the prepared NPs were characterised by UV-Drs spectroscopy. The valance state of Zinc ions and the role of Oxygen related defects were analysed from x-ray photoelectron spectroscopy (XPS) spectra. The electron paramagnetic resonance (EPR) spectral line illustrated the presence of complex defects such as Zinc interstitial (Zni) and oxygen vacancy (V+o) defects in the sample. The observed room temperature ferromagnetism (RTFM) in the prepared sample was induced by lattice defects. The observed results are discussed and reported.

  2. Platinum-group elements and minerals in the lower and middle group chromitites of the western Bushveld Complex, South Africa

    NASA Astrophysics Data System (ADS)

    Junge, Malte; Oberthür, Thomas; Osbahr, Inga; Gutter, Paul

    2016-10-01

    The chromitites of the Bushveld Complex in South Africa contain vast resources of platinum-group elements (PGE). However, knowledge of the distribution and the mineralogical siting of the PGE in the lower group (LG) and middle group (MG) chromitite seams of the Bushveld Complex is limited. We studied concentrates from the LG-6 and MG-2 chromitites of the western Bushveld Complex by a variety of microanalytical techniques. The dominant PGM are sulfides, namely laurite, cooperite-braggite, and malanite-cuprorhodsite, followed by PGE-sulfarsenides, sperrylite, and Pt-Fe alloys. Laurite is the most abundant PGM (vol%). The matching sets of PGM present in the LG and MG chromitites of both the western and the eastern Bushveld Complex, and in the UG-2 chromitite, show strong similarities which support the assumption of a characteristic and general chromitite-related PGM assemblage. Palladium and Rh contents in pentlandite are low and erratic although maximum contents of 7730 ppm Pd and 6020 ppm Rh were detected. Rare thiospinels of the polydymite-linnaeite-greigite series have PGE contents of 1430 ppm Pt, 5370 ppm Rh, and 1460 ppm Pd. The various PGE occur in different deportment: Platinum is generally present in the form of discrete PGM (sulfides, arsenides, alloys). Palladium is present as a large variety of discrete PGM and also incorporated in pentlandite. Rhodium forms discrete PGM and is occasionally present in pentlandite. The IPGE (Os, Ir, and Ru) are dominantly incorporated in laurite (often as inclusions in chromite) and also occur as sulfarsenides.

  3. Trace elements in organisms of different trophic groups in the White Sea

    NASA Astrophysics Data System (ADS)

    Budko, D. F.; Demina, L. L.; Martynova, D. M.; Gorshkova, O. M.

    2015-09-01

    Concentrations of trace elements (Fe, Mn, Cu, Pb, Ni, Cr, Cd, As, Co, and Se) have been studied in different trophic groups of organisms: primary producers (seston, presented mostly by phytoplankton), primary consumers (mesozooplankton, macrozooplankton, and bivalves), secondary consumers (predatory macrozooplankton and starfish), and consumers of higher trophic levels (fish species), inhabiting the coastal zone of Kandalaksha Bay and the White Sea (Cape Kartesh). The concentrations of elements differ significantly for the size groups of Sagitta elegans (zooplankton) and blue mussel Mytilus edulis, as well as for the bone and muscle tissues of studied fish species, Atlantic cod Gadus morhua marisalbi and Atlantic wolffish Anarhichas lupus. The concentrations of all the studied elements were lower among the primary consumers and producers, but increased again at higher trophic levels, from secondary consumers to tertiary consumers ("mesozooplankton → macrozooplankton Sagitta elegans" and "mussels → starfish"). Ni and Pb tended to decline through the food chains seston→…→cod and mesozooplankton→…→stickleback. Only the concentrations of Fe increased in all the trophic chains along with the increase of the trophic level.

  4. Structures and stabilities of group 17 fluorides EF3 (E = I, At, and element 117) with spin-orbit coupling.

    PubMed

    Yang, Dong-Dong; Wang, Fan

    2012-12-05

    In this work, a recently developed CCSD(T) approach with spin-orbit coupling (SOC) as well as density functional theory (DFT) using various exchange-correlation (XC) functionals are employed to investigate structures and stabilities of group 17 fluorides EF(3) (E = I, At, and element 117). These molecules are predicted to have bent T-shaped C(2v) structures according to the second-order Jahn-Teller (SOJT) effects or the valance shell electron pair repulsion (VSEPR) theory. For IF(3) and (117)F(3), our results are consistent with previous SOC-DFT calculations. However, different XC functionals provide different results for AtF(3) and our SOC-CCSD(T) calculations show that both the C(2v) and D(3h) structures are minima on the potential energy surface and the C(2v) structure is the global minimum for AtF(3). The performance of XC functionals on structures and stabilities of IF(3) and AtF(3) is found to depend on the fraction of the Hartree-Fock exchange (HFX) included in the XC functionals and the M06-2X functional with 54% of HFX providing results that agree best with CCSD(T) results. In addition, although both the C(2v) and D(3h) structures are minima for AtF(3), the energy barrier between them is only 8 kJ mol(-1) for the C(2v) structure and 0.05 kJ mol(-1) for the D(3h) structure. This indicates that the D(3h) structure could not possibly be observed experimentally and AtF(3) can convert easily between the three C(2v) structures. The SOJT term is shown to be reduced by electron correlation for IF(3) and AtF(3). On the other hand, although SOC decreases the energy difference between the C(2v) and D(3h) structures and reduces the deviation of the C(2v) structure from the D(3h) structure, it decreases the frequency of the bond bending mode, which may indicate that SOC actually increases the SOJT term. This could be related to mixing of spin-singlet E' states to low-energy spin-triplet states due to SOC.

  5. Composition, apparatus, and process, for sorption of gaseous compounds of group II-VII elements

    DOEpatents

    Tom, Glenn M.; McManus, James V.; Luxon, Bruce A.

    1991-08-06

    Scavenger compositions are disclosed, which have utility for effecting the sorptive removal of hazardous gases containing Group II-VII elements of the Periodic Table, such as are widely encountered in the manufacture of semiconducting materials and semiconductor devices. Gas sorption processes including the contacting of Group II-VII gaseous compounds with such scavenger compositions are likewise disclosed, together with critical space velocity contacting conditions pertaining thereto. Further described are gas contacting apparatus, including mesh structures which may be deployed in gas contacting vessels containing such scavenger compositions, to prevent solids from being introduced to or discharged from the contacting vessel in the gas stream undergoing treatment. A reticulate heat transfer structure also is disclosed, for dampening localized exothermic reaction fronts when gas mixtures comprising Group II-VII constituents are contacted with the scavenger compositions in bulk sorption contacting vessels according to the invention.

  6. Reactivity in the periphery of functionalised multiple bonds of heavier group 14 elements.

    PubMed

    Präsang, Carsten; Scheschkewitz, David

    2016-02-21

    Heavier group 14 multiple bonds have intrigued chemists since more than a century. The synthesis of stable compounds with double and triple bonds with silicon, germanium, tin and lead had considerable impact on modern ideas of chemical bonding. These developments were made possible by the use of bulky substituents that provide kinetic and thermodynamic protection. Since about a decade the compatibility of heavier multiple bonds with various functional groups has moved into focus. This review covers multiply bonded group 14 species with at least one additional reactive site. The vinylic functionalities of groups 1 and 17, resulting in nucleophilic and electrophilic disila vinyl groups, respectively, are the most prevalent and well-studied. They have been employed repeatedly for the transfer of heavier multiple bonds to yield low-valent group 14 compounds with novel structural motifs. Vinylic functionalities of groups 2 to 16 and a few σ-bonded transition metal complexes are experimentally known, but their reactivity has been studied to a lesser extent. Donor-coordinated multiple bonds are a relatively new field of research, but the large degree of unsaturation as isomers of alkynes (as well as residual functionality in some cases) offers considerable possibility for further manipulation, e.g. for the incorporation into more extended systems. Heavier allyl halides constitute the major part of heavier multiple bonds with a functional group in allylic position and some examples of successful transformations are given. At present, remote functionalities are basically limited to para-phenylene functionalised disilenes. The reported use of the latter for further derivatisation might encourage investigations in this direction. In summary, the study of peripherally functionalised multiple bonds with heavier group 14 elements is already well beyond its infancy and may be an instrumental factor in awakening the potential of group 14 chemistry for applications in polymers and

  7. Leaves of Phragmites australis as potential atmospheric biomonitors of Platinum Group Elements.

    PubMed

    Bonanno, Giuseppe; Pavone, Pietro

    2015-04-01

    The increasing emissions of Platinum Group Elements (PGEs), namely Pt, Pd and Rh, may pose a significant risk to ecosystem processes and human health. A periodic assessment of PGEs distribution in the environment is thus of the utmost importance for the implementation of timely measures of mitigation. Although several studies have quantified PGEs in different life forms such as mammals, birds, fish, crustaceans, algae, mosses and even human beings, data about vascular plants need further surveys. This study aimed to test the suitability of the grass Phragmites australis (common reed) as a biomonitor of PGEs atmospheric pollution. The results showed that Pd and Pt concentrations in leaves are significantly higher in urban areas. In particular, Pd showed the highest range of values in line with current studies that consider palladium as the main element of traffic-related pollution. Overall, the leaves of Phragmites australis reflected the different gradient of PGEs emissions, and may thus be considered as potential biomonitors of atmospheric pollution.

  8. Determination of copper, scandium, molybdenum, tin, lead, and iron group elements in lunar surface materials

    NASA Technical Reports Server (NTRS)

    Pavlenko, L. I.; Simonova, L. V.; Karyakin, A. V.

    1974-01-01

    Distribution regularities of copper, scandium, molybdenum, tin, lead, and iron group elements were investigated in basaltoid rocks of lunar and terrestrial origin. Samples of various regolith zones taken in the area of the Sea of Fertility were analyzed, along with samples of basic and ultrabasic rocks of the East African Rift for their content of the trace admixtures listed. Data obtained on the abundance of copper, scandium, molybdenum, tin, lead, cobalt, nickel, chromium, and vanadium in Luna 16 lunar surface material were compared with the abundance of these elements in samples of lunar rocks returned by Apollo 11, Apollo 12, and Apollo 14, with the exception of scandium; its content in the latter samples was considerably higher.

  9. The VIPER elements of trypanosomes constitute a novel group of tyrosine recombinase-enconding retrotransposons.

    PubMed

    Lorenzi, Hernan A; Robledo, German; Levin, Mariano J

    2006-02-01

    VIPER was initially characterized as a 2326bp LTR-like retroelement associated to SIRE, a short interspersed repetitive element specific of Trypanosoma cruzi. It carried a single ORF that coded for a putative reverse transcriptase-RNAse H protein, suggesting that it could be a truncated copy of a longer retroelement. Herein we report the identification and characterization of a complete 4480bp long VIPER in the T. cruzi genome. The complete VIPER harbored three non-overlapped domains encoding for a GAG-like, a tyrosine recombinase and a reverse transcriptase-RNAse H proteins. VIPER elements were also found in the genomes of Trypanosoma brucei and Trypanosoma vivax, but not in Leishmania sp. On the basis of its reverse transcriptase phylogeny, VIPER was classified as an LTR retroelement. However, VIPER was structurally related to the tyrosine recombinase encoding retroelements, DIRS and Ngaro. Phylogenetic analysis showed that VIPER's tyrosine recombinase grouped with the transposases RCI1 of Escherichia coli and Ye24 and Ye72 of Haemophilus influenzae within a major branch of prokaryotic recombinases. Taken together, VIPER's structure, the nature of its tyrosine recombinase, the unique features of its reverse transcriptase catalytic consensus motif and the fact that it was found in Trypanosomes, an early branching eukaryote, suggest that VIPER may be the closest relative of the founder element of the tyrosine recombinase encoding retrotransposons known up to date. Our analysis revealed that tyrosine recombinase-encoding retroelements were originated as early in evolution as non-LTR retroelements and suggests that VIPER, Ngaro and DIRS elements may constitute a third group of retrotransposons, distinct from both LTR and non-LTR retroelements.

  10. 33 CFR 155.1052 - Response plan development and evaluation criteria for vessels carrying group V petroleum oil as a...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... evaluation criteria for vessels carrying group V petroleum oil as a primary cargo. 155.1052 Section 155.1052....1052 Response plan development and evaluation criteria for vessels carrying group V petroleum oil as a primary cargo. (a) Owners and operators of vessels that carry group V petroleum oil as a primary...

  11. 33 CFR 155.1052 - Response plan development and evaluation criteria for vessels carrying group V petroleum oil as a...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... evaluation criteria for vessels carrying group V petroleum oil as a primary cargo. 155.1052 Section 155.1052....1052 Response plan development and evaluation criteria for vessels carrying group V petroleum oil as a primary cargo. (a) Owners and operators of vessels that carry group V petroleum oil as a primary...

  12. 33 CFR 155.5052 - Response plan development and evaluation criteria for nontank vessels carrying group V petroleum...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... evaluation criteria for nontank vessels carrying group V petroleum oil. 155.5052 Section 155.5052 Navigation... Response plan development and evaluation criteria for nontank vessels carrying group V petroleum oil. Owners or operators of nontank vessels that carry group V petroleum oil as fuel or cargo must meet...

  13. 33 CFR 155.1052 - Response plan development and evaluation criteria for vessels carrying group V petroleum oil as a...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... evaluation criteria for vessels carrying group V petroleum oil as a primary cargo. 155.1052 Section 155.1052....1052 Response plan development and evaluation criteria for vessels carrying group V petroleum oil as a primary cargo. (a) Owners and operators of vessels that carry group V petroleum oil as a primary...

  14. 33 CFR 155.1052 - Response plan development and evaluation criteria for vessels carrying group V petroleum oil as a...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... evaluation criteria for vessels carrying group V petroleum oil as a primary cargo. 155.1052 Section 155.1052....1052 Response plan development and evaluation criteria for vessels carrying group V petroleum oil as a primary cargo. (a) Owners and operators of vessels that carry group V petroleum oil as a primary...

  15. 33 CFR 155.1052 - Response plan development and evaluation criteria for vessels carrying group V petroleum oil as a...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... evaluation criteria for vessels carrying group V petroleum oil as a primary cargo. 155.1052 Section 155.1052....1052 Response plan development and evaluation criteria for vessels carrying group V petroleum oil as a primary cargo. (a) Owners and operators of vessels that carry group V petroleum oil as a primary...

  16. pH-dependent release of trace elements including platinum group elements (PGEs) from gasoline and diesel catalysts

    NASA Astrophysics Data System (ADS)

    Sucha, Veronika; Mihaljevic, Martin; Ettler, Vojtech; Strnad, Ladislav

    2014-05-01

    The release of trace metals and platinum group elements (PGEs) from automobile exhaust catalysts represents a remarkable source of higly dispersed environmental contamination. Especially, PGEs have shown increasing research interest due to their possible bioaccessibility. In our research, we focused on leaching behaviour of trace metals from gasoline and diesel automobile catalysts. While catalysts for gasoline engines contain a mixture of Pt-Pd-Rh or Pd-Rh, catalysts for diesel engines are composed only of Pt. We used dust from two crushed gasoline and two crushed diesel catalysts (new and aged). The dust of gasoline catalysts contains significant concentrations of Pt (700 mg.kg-1), Pd (11 000 mg.kg-1) and Rh (700 mg.kg-1). And the dust of diesel catalysts are composed of Pt (3 900 mg.kg-1) and they contains negligible amounts of Pd dan Rh (< 0.5 mg.kg-1, < 0.1 mg.kg-1, respectively). To evaluate leaching of trace metals from dust we used pH-stat leaching test according to the European standard CEN/TS 14997. The concentrations of cations: PGEs (Pt, Pd a Rh), K, Na, Ca, Mg, Al, Ti, Cr, Mn, Fe, Co, Ni, Cu, Zn, Cd, Pb, La and Ce were determined by inductively coupled plasma mass spectrometry (ICP-MS) and atomic absorption spectrometry (AAS), and anions: F-, Cl-, SO42- and NO3- by high-performance liquid chromatography. Although the dusts from catalysts were relatively stable to acid/base influence, the leaching of trace metals from catalysts showed a dependence on pH. Generally, the highest concentrations were released under acidic conditions. The leaching of PGEs was higher for Pt in diesel catalysts and for Pd and Rh in gasoline catalysts. The highest concentrations of Zn and Pb were observed in old catalysts. The rare earth metals were released more from gasoline catalysts. Catalysts particles represent health risk especially with respect to their PGEs contents.

  17. Multiple complexation of CO and related ligands to a main-group element

    NASA Astrophysics Data System (ADS)

    Braunschweig, Holger; Dewhurst, Rian D.; Hupp, Florian; Nutz, Marco; Radacki, Krzysztof; Tate, Christopher W.; Vargas, Alfredo; Ye, Qing

    2015-06-01

    The ability of an atom or molecular fragment to bind multiple carbon monoxide (CO) molecules to form multicarbonyl adducts is a fundamental trait of transition metals. Transition-metal carbonyl complexes are vital to industry, appear naturally in the active sites of a number of enzymes (such as hydrogenases), are promising therapeutic agents, and have even been observed in interstellar dust clouds. Despite the wealth of established transition-metal multicarbonyl complexes, no elements outside groups 4 to 12 of the periodic table have yet been shown to react directly with two or more CO units to form stable multicarbonyl adducts. Here we present the synthesis of a borylene dicarbonyl complex, the first multicarbonyl complex of a main-group element prepared using CO. The compound is additionally stable towards ambient air and moisture. The synthetic strategy used--liberation of a borylene ligand from a transition metal using donor ligands--is broadly applicable, leading to a number of unprecedented monovalent boron species with different Lewis basic groups. The similarity of these compounds to conventional transition-metal carbonyl complexes is demonstrated by photolytic liberation of CO and subsequent intramolecular carbon-carbon bond activation.

  18. OTX2 Activity at Distal Regulatory Elements Shapes the Chromatin Landscape of Group 3 Medulloblastoma.

    PubMed

    Boulay, Gaylor; Awad, Mary E; Riggi, Nicolo; Archer, Tenley C; Iyer, Sowmya; Boonseng, Wannaporn E; Rossetti, Nikki E; Naigles, Beverly; Rengarajan, Shruthi; Volorio, Angela; Kim, James C; Mesirov, Jill P; Tamayo, Pablo; Pomeroy, Scott L; Aryee, Martin J; Rivera, Miguel N

    2017-02-17

    Medulloblastoma is the most frequent malignant pediatric brain tumor and is divided into at least four subgroups known as WNT, SHH, Group 3, and Group 4. Here, we characterized gene regulation mechanisms in the most aggressive subtype, Group 3 tumors, through genome-wide chromatin and expression profiling. Our results show that most active distal sites in these tumors are occupied by the transcription factor OTX2. Highly active OTX2-bound enhancers are often arranged as clusters of adjacent peaks and are also bound by the transcription factor NEUROD1. These sites are responsive to OTX2 and NEUROD1 knockdown and could also be generated de novo upon ectopic OTX2 expression in primary cells, showing that OTX2 cooperates with NEUROD1 and plays a major role in maintaining and possibly establishing regulatory elements as a pioneer factor. Among OTX2 target genes, we identified the kinase NEK2, whose knockdown and pharmacologic inhibition decreased cell viability. Our studies thus show that OTX2 controls the regulatory landscape of Group 3 medulloblastoma through cooperative activity at enhancer elements and contributes to the expression of critical target genes.SIGNIFICANCE: The gene regulation mechanisms that drive medulloblastoma are not well understood. Using chromatin profiling, we find that the transcription factor OTX2 acts as a pioneer factor and, in cooperation with NEUROD1, controls the Group 3 medulloblastoma active enhancer landscape. OTX2 itself or its target genes, including the mitotic kinase NEK2, represent attractive targets for future therapies. Cancer Discov; 7(3); 1-14. ©2017 AACR.

  19. Controlled Synthesis of Polyions of Heavy Main-Group Elements in Ionic Liquids

    PubMed Central

    Groh, Matthias F.; Wolff, Alexander; Grasser, Matthias A.; Ruck, Michael

    2016-01-01

    Ionic liquids (ILs) have been proven to be valuable reaction media for the synthesis of inorganic materials among an abundance of other applications in different fields of chemistry. Up to now, the syntheses have remained mostly “black boxes”; and researchers have to resort to trial-and-error in order to establish a new synthetic route to a specific compound. This review comprises decisive reaction parameters and techniques for the directed synthesis of polyions of heavy main-group elements (fourth period and beyond) in ILs. Several families of compounds are presented ranging from polyhalides over carbonyl complexes and selenidostannates to homo and heteropolycations. PMID:27598123

  20. Study on 12kV outdoor vacuum switch with replaceable HRC element drop out fuse

    SciTech Connect

    Wang Jiimei

    1996-12-31

    A new type of vacuum interrupter for 12kV outdoor vacuum switch was experimentally studied, the envelope of which was made of porcelain with petticoat flange for outdoor insulation. In order to produce an axial magnetic field and improve the capacity of transfer current in the vacuum interrupter, an iron plate of horse-shoe construction ingeniously designed was chosen as an electrode. The drop-out fuse with replaceable sand-filled HRC element in series with the vacuum switch is a new conception of design to increase breaking capacity. However, it is a vacuum switch of newly designed to form {open_quotes}a vacuum switch and drop-out type fuse combination{close_quotes}.

  1. Coronal Element Abundances of the Post-Common Envelope Binary V471 Tauri with ASCA

    NASA Technical Reports Server (NTRS)

    Still, Martin; Hussain, Gaitee; White, Nicholas E. (Technical Monitor)

    2002-01-01

    We report on ASCA observations of the coronally active companion star in the post-common envelope binary V471 Tau. While it would be prudent to check the following results with grating spectroscopy, we find that a single-temperature plasma model does not fit the data. Two temperature models with variable abundances indicate that Fe is underabundant compared to the Hyades photospheric mean, whereas, the high first ionization potential element Ne is overabundant. This is indicative of the inverse first ionization effect, believed to result from the fractionation of ionized material by the magnetic field in the upper atmosphere of the star. Evolutionary calculations indicate that there should be no peculiar abundances on the companion star resulting from the common envelope epoch. Indeed, we find no evidence for peculiar abundances, although uncertainties are high.

  2. Analyses of platinum group elements in mosses as indicators of road traffic emissions in Austria

    NASA Astrophysics Data System (ADS)

    Zechmeister, Harald G.; Hagendorfer, Harald; Hohenwallner, Daniela; Hanus-Illnar, Andrea; Riss, Alarich

    The concentrations of platinum group elements (PGE; platinum, palladium, rhodium) and 17 other elements in mosses growing at 32 sampling sites along 12 roads in Austria were analysed. The study included passive monitoring of naturally growing mosses with an experimental design using mosses samples exposed in a tunnel experiment. PGEs (Pt, Pd, Rh) were analysed by ICP-MS (ELAN DRC II, Perkin Elmer SCIEX) according to EN ISO 17294-2 Tl.29. Mean concentrations of PGEs in five moss species were: Pt 7.07±9.97, Pd 2.8±5.2 und Rh 0.6±0.8 ng g -1 dry weight. This is comparable to data derived from measurements of gasoline autocatalyst emissions or airborne particles (<10 μm). Compared to soils and road dust along highways, concentrations in mosses were lower by a factor of ten, compared to grasses they were comparable or somewhat higher. The ratios between the various PGEs were calculated as follows (mean values): Pt/Pd 7.9±10.2, Pt/Rh 12.6±8.3 and Pd/Rh 3.7±2.2. The number of light duty vehicles (<3.5 t) and the distance from the road were the main influential factors for PGE concentrations. Especially strong correlations could be found between Pt and Sb, Cu, Zn, and Cd (in decreasing order), which are all elements derived mainly from road traffic emissions. Cluster analysis (Partioning Around Medoids Method) separated elements derived mainly from soil dust (Ca, Al). An analysis of spatial deposition patterns of PGEs showed a reciprocal decrease of concentrations with increasing distance from the road, reaching background values at distances between 10 and 200 m, sometimes even more, but outside the spatial range of our investigation.

  3. On the role of group I elements in ZnO

    NASA Astrophysics Data System (ADS)

    Meyer, B. K.; Stehr, J.; Hofstaetter, A.; Volbers, N.; Zeuner, A.; Sann, J.

    2007-07-01

    Diffusion of Li, Na and K into single-crystal substrates of ZnO was performed. We compare the results with ZnO epitaxial films doped with the respective elements during growth. The diffused and in-situ doped layers were studied using mass spectroscopy and low temperature photoluminescence spectroscopy. Li and Na are known to produce deep acceptor centers which give rise to shallow donor to deep acceptor recombinations in the visible spectral region. We will demonstrate that shallow acceptors are also introduced, having binding energies around 300 meV. A donor acceptor pair recombination (zero phonon line at 3.05 eV) with LO phonon replica is observed. We further investigated bulk ZnO crystals which contained the deep Li acceptor by thermal treatments under H2 atmospheres. With increasing annealing temperature shallow donors are introduced as monitored by EPR while the EPR signal of the neutral Li acceptors decreases. Quite unexpectedly, the shallow Li acceptor centre which is not present in the as-grown state is also created.

  4. Elemente der beiden W-UMa-Sterne GSC 0424-0792 (Brh V62) und GSC 1721-1591 (Brh V127)

    NASA Astrophysics Data System (ADS)

    Bernhard, Klaus; Frank, Peter; Moschner, Wolfgang

    2011-01-01

    CCD observations and ASAS-3 data of GSC 0424-0792 (Brh V62) and GSC 1721-1591 (Brh V127) lead to the following elements and types of variability: GSC 0424-0792: HJD (MinI)= 2453142.489(5)+ E*1.182336(1), type: WUMa GSC 1721-1591: HJD (MinI)= 2455429.5086(4)+E*0.3188963(1), type: WUMa

  5. Interest Groups, the Courts, and Educational Equality: A Policy Regimes Approach to "Vergara v. California"

    ERIC Educational Resources Information Center

    Superfine, Benjamin Michael; Thompson, Alea R.

    2016-01-01

    In "Vergara v. California" (2014), a trial-level court ruled that California laws governing teacher tenure and dismissal were unconstitutional. This study analyzes "Vergara" in light of the shifting use of the courts to promote equal educational opportunities and the changing power bases of educational interest groups,…

  6. Should an obsessive-compulsive spectrum grouping of disorders be included in DSM-V?

    PubMed

    Phillips, Katharine A; Stein, Dan J; Rauch, Scott L; Hollander, Eric; Fallon, Brian A; Barsky, Arthur; Fineberg, Naomi; Mataix-Cols, David; Ferrão, Ygor Arzeno; Saxena, Sanjaya; Wilhelm, Sabine; Kelly, Megan M; Clark, Lee Anna; Pinto, Anthony; Bienvenu, O Joseph; Farrow, Joanne; Leckman, James

    2010-06-01

    The obsessive-compulsive (OC) spectrum has been discussed in the literature for two decades. Proponents of this concept propose that certain disorders characterized by repetitive thoughts and/or behaviors are related to obsessive-compulsive disorder (OCD), and suggest that such disorders be grouped together in the same category (i.e. grouping, or "chapter") in DSM. This article addresses this topic and presents options and preliminary recommendations to be considered for DSM-V. The article builds upon and extends prior reviews of this topic that were prepared for and discussed at a DSM-V Research Planning Conference on Obsessive-Compulsive Spectrum Disorders held in 2006. Our preliminary recommendation is that an OC-spectrum grouping of disorders be included in DSM-V. Furthermore, we preliminarily recommend that consideration be given to including this group of disorders within a larger supraordinate category of "Anxiety and Obsessive-Compulsive Spectrum Disorders." These preliminary recommendations must be evaluated in light of recommendations for, and constraints upon, the overall structure of DSM-V.

  7. Should an Obsessive-Compulsive Spectrum Grouping of Disorders Be Included in DSM-V?

    PubMed Central

    Phillips, Katharine A.; Stein, Dan J.; Rauch, Scott; Hollander, Eric; Fallon, Brian A.; Barsky, Arthur; Fineberg, Naomi; Mataix-Cols, David; Ferrão, Ygor Arzeno; Saxena, Sanjaya; Wilhelm, Sabine; Kelly, Megan M.; Clark, Lee Anna; Pinto, Anthony; Bienvenu, O. Joseph; Farrow, Joanne; Leckman, James

    2014-01-01

    The obsessive-compulsive (OC) spectrum has been discussed in the literature for two decades. Proponents of this concept propose that certain disorders characterized by repetitive thoughts and/or behaviors are related to obsessive-compulsive disorder (OCD), and suggest that such disorders be grouped together in the same category (i.e., grouping, or “chapter”) in DSM. This paper addresses this topic and presents options and preliminary recommendations to be considered for DSM-V. The paper builds upon and extends prior reviews of this topic that were prepared for and discussed at a DSM-V Research Planning Conference on Obsessive-Compulsive Spectrum Disorders held in 2006. Our preliminary recommendation is that an OC-spectrum grouping of disorders be included in DSM-V. Furthermore, we preliminarily recommend that consideration be given to including this group of disorders within a larger supraordinate category of “Anxiety and Obsessive-Compulsive Spectrum Disorders.” These preliminary recommendations must be evaluated in light of recommendations for, and constraints upon, the overall structure of DSM-V. PMID:20533367

  8. Calculating three loop ladder and V-topologies for massive operator matrix elements by computer algebra

    NASA Astrophysics Data System (ADS)

    Ablinger, J.; Behring, A.; Blümlein, J.; De Freitas, A.; von Manteuffel, A.; Schneider, C.

    2016-05-01

    Three loop ladder and V-topology diagrams contributing to the massive operator matrix element AQg are calculated. The corresponding objects can all be expressed in terms of nested sums and recurrences depending on the Mellin variable N and the dimensional parameter ε. Given these representations, the desired Laurent series expansions in ε can be obtained with the help of our computer algebra toolbox. Here we rely on generalized hypergeometric functions and Mellin-Barnes representations, on difference ring algorithms for symbolic summation, on an optimized version of the multivariate Almkvist-Zeilberger algorithm for symbolic integration, and on new methods to calculate Laurent series solutions of coupled systems of differential equations. The solutions can be computed for general coefficient matrices directly for any basis also performing the expansion in the dimensional parameter in case it is expressible in terms of indefinite nested product-sum expressions. This structural result is based on new results of our difference ring theory. In the cases discussed we deal with iterative sum- and integral-solutions over general alphabets. The final results are expressed in terms of special sums, forming quasi-shuffle algebras, such as nested harmonic sums, generalized harmonic sums, and nested binomially weighted (cyclotomic) sums. Analytic continuations to complex values of N are possible through the recursion relations obeyed by these quantities and their analytic asymptotic expansions. The latter lead to a host of new constants beyond the multiple zeta values, the infinite generalized harmonic and cyclotomic sums in the case of V-topologies.

  9. Permissive tracts for nickel, copper, platinum group elements (PGE), and chromium deposits of Mauritania (phase V, deliverable 66): Chapter G1 in Second projet de renforcement institutionnel du secteur minier de la République Islamique de Mauritanie (PRISM-II)

    USGS Publications Warehouse

    Taylor, Cliff D.; Horton, John D.

    2012-01-01

    This report contains the USGS results of the PRISM-II Mauritania Minerals Project and is presented in cooperation with the Ministry of Petroleum, Energy, and Mines of the Islamic Republic of Mauritania. The Report is composed of separate chapters consisting of multidisciplinary interpretive reports with accompanying plates on the geology, structure, geochronology, geophysics, hydrogeology, geochemistry, remote sensing (Landsat TM and ASTER), and SRTM and ASTER digital elevation models of Mauritania. The syntheses of these multidisciplinary data formed the basis for additional chapters containing interpretive reports on 12 different commodities and deposit types known to occur in Mauritania, accompanied by countrywide mineral resource potential maps of each commodity/deposit type. The commodities and deposit types represented include: (1) Ni, Cu, PGE, and Cr deposits hosted in ultramafic rocks; (2) orogenic, Carlin-like, and epithermal gold deposits; (3) polymetallic Pb-Zn-Cu vein deposits; (4) sediment-hosted Pb-Zn-Ag deposits of the SEDEX and Mississippi Valley-type; (5) sediment-hosted copper deposits; ( 6) volcanogenic massive sulfide deposits; (7) iron oxide copper-gold deposits; (8) uranium deposits; (9) Algoma-, Superior-, and oolitic-type iron deposits; (10) shoreline Ti-Zr placer deposits; (11) incompatible element deposits hosted in pegmatites, alkaline rocks, and carbonatites, and; (12) industrial mineral deposits. Additional chapters include the Mauritanian National Mineral Deposits Database are accompanied by an explanatory text and the Mauritania Minerals Project GIS that contains all of the interpretive layers created by USGS scientists. Raw data not in the public domain may be obtained from the Ministry of Petroleum, Energy, and Mines in Nouakchott, Mauritania.

  10. Site preference of alloying elements in DO22-Ni3V phase: Phase-field and first-principles study

    NASA Astrophysics Data System (ADS)

    Zhang, Ding-Ni; Shangguan, Qian-Qian; Liu, Fu; Zhang, Ming-Yi

    2015-07-01

    Site preference of alloying elements in DO22-Ni3V phase was investigated using phase-field and first-principles method. The concentrations of alloying elements on sublattices of DO22-Ni3V phase were quantitatively studied using phase-field model based on microscopic diffusion equations. The phase-field computation results demonstrate that the concentration differences of alloying elements on the NiI and NiII site are attributed to the coordination environment difference. Host atoms Ni and substitutional ternary additions Al prefer to occupy NiI site. Antisite atoms V show site preference on the NiII site. Further reason of site preference of alloying elements on the two different Ni sites were studied using first-principles method to calculate the electronic structure of DO22-Ni3V phase. Calculation of density of states, orbitals population and charge population of the optimized Ni3V structure found that the electronic structures of NiI and NiII sites are different. Electronic structure difference, which is caused by coordination environment difference, is the essential reason for site selectivity behaviors of alloying elements on NiI and NiII sites.

  11. CSRL-V ENDF/B-V 227-group neutron cross-section library and its application to thermal-reactor and criticality safety benchmarks

    SciTech Connect

    Ford, W.E. III; Diggs, B.R.; Knight, J.R.; Greene, N.M.; Petrie, L.M.; Webster, C.C.; Westfall, R.M.; Wright, R.Q.; Williams, M.L.

    1982-01-01

    Characteristics and contents of the CSRL-V (Criticality Safety Reference Library based on ENDF/B-V data) 227-neutron-group AMPX master and pointwise cross-section libraries are described. Results obtained in using CSRL-V to calculate performance parameters of selected thermal reactor and criticality safety benchmarks are discussed.

  12. Combined AIE/EBE/GMRES approach to incompressible flows. [Adaptive Implicit-Explicit/Grouped Element-by-Element/Generalized Minimum Residuals

    NASA Technical Reports Server (NTRS)

    Liou, J.; Tezduyar, T. E.

    1990-01-01

    Adaptive implicit-explicit (AIE), grouped element-by-element (GEBE), and generalized minimum residuals (GMRES) solution techniques for incompressible flows are combined. In this approach, the GEBE and GMRES iteration methods are employed to solve the equation systems resulting from the implicitly treated elements, and therefore no direct solution effort is involved. The benchmarking results demonstrate that this approach can substantially reduce the CPU time and memory requirements in large-scale flow problems. Although the description of the concepts and the numerical demonstration are based on the incompressible flows, the approach presented here is applicable to larger class of problems in computational mechanics.

  13. Tailoring of ZnO with selected group-II elements for LED materials

    NASA Astrophysics Data System (ADS)

    Saleem, Murtaza; Manzoor, Adnan; Zaffar, Mohammed; Hussain, Syed Zajif; Anwar, M. Sabieh

    2016-06-01

    The semiconductor ZnO is a promising candidate for its applications in light-emitting diodes. In this study ZnO nanostructures tailored with selected group-II elements were synthesized using sol-gel-based fuel-agent-assistive chemical technique. Structural studies from X-ray diffraction analysis revealed the presence of wurtzite hexagonal crystal structure in all compositions confirming the stability of the Mg-doped structure while indicating presence of some traces of un-reacted and oxides of Sr and Ba in other compositions. Lattice parameters, crystallite size, lattice strain, density, and cell volume were extracted from X-ray diffraction data. Morphology and elemental composition analysis showed exact correlation with structural arrangements. The size of particles was also observed with dynamic light-scattering measurements. Absorbance and electrical transport studies were performed using UV-Vis spectrophotometry and four-probe measurements, respectively; the former was used to estimate the band gap of nanostructures. Energy-dispersive X-ray analysis was employed for confirming the substitution of Mg, Sr, and Ba atoms at Zn and O sites. Band gap values show strong dependence upon the tailored ZnO compositions.

  14. Characterization of the Sukinda and Nausahi ultramafic complexes, Orissa, India by platinum-group element geochemistry

    USGS Publications Warehouse

    Page, N.J.; Banerji, P.K.; Haffty, J.

    1985-01-01

    Samples of 20 chromitite, 14 ultramafic and mafic rock, and 9 laterite and soil samples from the Precambrian Sukinda and Nausahi ultramafic complexes, Orissa, India were analyzed for platinum-group elements (PGE). The maximum concentrations are: palladium, 13 parts per billion (ppb); platinum, 120 ppb; rhodium, 21 ppb; iridium, 210 ppb; and ruthenium, 630 ppb. Comparison of chondrite-normalized ratios of PGE for the chromitite samples of lower Proterozoic to Archean age with similar data from Paleozoic and Mesozoic ophiolite complexes strongly implies that these complexes represent Precambrian analogs of ophiolite complexes. This finding is consistent with the geology and petrology of the Indian complexes and suggests that plate-tectonic and ocean basin developement models probably apply to some parts of Precambrian shield areas. ?? 1985.

  15. Accumulation of platinum group elements by the marine gastropod Littorina littorea.

    PubMed

    Mulholland, Rachel; Turner, Andrew

    2011-04-01

    The accumulation and trophic transfer of the platinum group elements (PGE): Rh, Pd and Pt; have been studied in short-term (5 day) exposures conducted in aquaria containing the marine macroalga, Ulva lactuca, and/or the grazing mollusc, Littorina littorea. Metals added to sea water (to concentrations of 20 μg L⁻¹) were taken up by U. lactuca in the order Rh, Pt > Pd and by L. littorea in the order Pd ≥ Pt ≥ Rh, with greatest metal accumulation in the latter generally occurring in the visceral complex and kidney. When fed contaminated alga, accumulation of Rh and Pd by L. littorea, relative to total available metal, increased by an order of magnitude, while accumulation of Pt was not readily detected. We conclude that the diet is the most important vector for accumulation of Rh and Pd, while accumulation of Pt appears to proceed mainly from the aqueous phase.

  16. Ab initio effective core potentials for molecular calculations. Potentials for main group elements Na to Bi

    SciTech Connect

    Wadt, W.R.; Hay, P.J.

    1985-01-01

    A consistent set of ab initio effective core potentials (ECP) has been generated for the main group elements from Na to Bi using the procedure originally developed by Kahn. The ECP's are derived from all-electron numerical Hartree--Fock atomic wave functions and fit to analytical representations for use in molecular calculations. For Rb to Bi the ECP's are generated from the relativistic Hartree--Fock atomic wave functions of Cowan which incorporate the Darwin and mass--velocity terms. Energy-optimized valence basis sets of (3s3p) primitive Gaussians are presented for use with the ECP's. Comparisons between all-electron and valence-electron ECP calculations are presented for NaF, NaCl, Cl/sub 2/, Cl/sub 2//sup -/, Br/sub 2/, Br/sub 2//sup -/, and Xe/sub 2//sup +/. The results show that the average errors introduced by the ECP's are generally only a few percent.

  17. What Factors Control Platinum-Group Element (PGE) Abundances in Basalts From the Ontong Java Plateau?

    NASA Astrophysics Data System (ADS)

    Chazey, W. J.; Neal, C. R.

    2002-12-01

    Eleven samples encompassing four sites drilled by Ocean Drilling Program Leg 192 to the Ontong Java Plateau (OJP) were analyzed for major, trace and platinum-group (PGEs: Ir, Ru, Rh, Pt, and Pd) elements. Based on major and trace element chemistry, these are divided into two groups: a primitive group, which was newly discovered on Leg 192, and Kwaimbaita-type basalts, which are ubiquitous on the OJP (cf. Tejada et al., 2002, J. Pet. 43:449). The primitive group is relatively enriched in MgO, Ni, and Cr and relatively depleted in incompatible elements compared to the Kwaimbaita-type basalts. Petrography indicates that the fractionating phases during emplacement of both types of basalts were olivine and Cr-spinel +/- plagioclase +/- cpx. Normalized PGE profiles are fractionated, but exhibit a flattening between Ru and Ir and occasionally an enrichment in Ir. It has been shown that chromite can preferentially incorporate Os and Ru (Kd ?150) over Ir (Kd ?100), which may account for the Ir and Ru systematics. We do not consider sulfide to be a factor in fractionating the PGEs because it is either absent or present as a trace phase in these basalts and the OJP basalts are sulfur undersaturated (Michael and Cornell, 1996, EOS 77:714). Additionally, the primitive samples from the OJP also have Cu/Pd ratios (4500-8000) that are roughly similar to primitive mantle (7300), and have a generally flat transition from Pd to Y on a primitive mantle-normalized plot. It is unlikely that these samples reached sulfur saturation. The Kwaimbaita-type basalts have slightly elevated Cu/Pd ratios (9000-14000). While there are subtle differences between the PGE profiles of basalts from the Leg 192 drill cores compared to OJP basalts from subaerial outcrops in the Solomon Islands (e.g., the former have general lower Pt/Rh and higher Rh/Ru ratios), it is apparent that silicate and oxide phases are controlling the PGE profiles and abundances. For example, the six samples analyzed from Site

  18. Improved and Expanded Near-IR Oscillator Strengths for Fe-group Elements

    NASA Astrophysics Data System (ADS)

    Wood, Michael; Nave, Gillian; Sneden, Christopher Alan

    2015-08-01

    The use of modern experimental techniques, including LIF lifetime and FTS branching fraction measurements, has significantly increased the scope and reliability of laboratory atomic transition probabilities in the UV and visible. However, this combination of techniques is problematic in the IR, a region of increasing importance due to improved detector, spectrometer, and telescope technologies. The result is a significant gap between the capabilities to record new IR astronomical spectra and the data needed to sufficiently analyze them. To aid in closing this gap, we are incorporating new techniques, including reverse stellar analyses, to measure sets of oscillator strengths in the near-IR (λ ≈ 1-5 μm), with a primary focus on the Fe-group elements. A description of the methods and their applicability will be presented, including recent results for Ti I.

  19. Platinum-group element geochemistry of zoned ultramafic intrusive suites, Klamath Mountains, California and Oregon.

    USGS Publications Warehouse

    Gray, F.; Page, N.J.; Carlson, C.A.; Wilson, S.A.; Carlson, R.R.

    1986-01-01

    Analyses for platinum-group elements of the varied rock suites of three Alaskan-type ultramafic to mafic multi-intrusive bodies are reported. Ir and Ru are less than analytical sensitivities of 100 and 20 ppb; Rh is less than or near 1 ppb. Average Pd assays vary among the rocks within intrusive complexes and between the three complexes (6.3, 13.7, 36.4 ppb); average Pt assays vary little among the same samples (27.9, 60.9, 34.0 ppb). Statistically adjusted Pt/(Pt + Pd) ratios increase in each suite from gabbro through clinopyroxenite to olivine-rich rocks, possibly owing to Pd fractionation.-G.J.N.

  20. Report of the IAU Working Group on cartographic coordinates and rotational elements: 2009

    USGS Publications Warehouse

    Archinal, B.A.; A'Hearn, M.F.; Bowell, E.; Conrad, A.; Consolmagno, G.J.; Courtin, R.; Fukushima, T.; Hestroffer, D.; Hilton, J.L.; Krasinsky, G.A.; Neumann, G.; Oberst, J.; Seidelmann, P.K.; Stooke, P.; Tholen, D.J.; Thomas, P.C.; Williams, I.P.

    2010-01-01

    Every three years the IAU Working Group on Cartographic Coordinates and Rotational Elements revises tables giving the directions of the poles of rotation and the prime meridians of the planets, satellites, minor planets, and comets. This report takes into account the IAU Working Group for Planetary System Nomenclature (WGPSN) and the IAU Committee on Small Body Nomenclature (CSBN) definition of dwarf planets, introduces improved values for the pole and rotation rate of Mercury, returns the rotation rate of Jupiter to a previous value, introduces improved values for the rotation of five satellites of Saturn, and adds the equatorial radius of the Sun for comparison. It also adds or updates size and shape information for the Earth, Mars’ satellites Deimos and Phobos, the four Galilean satellites of Jupiter, and 22 satellites of Saturn. Pole, rotation, and size information has been added for the asteroids (21) Lutetia, (511) Davida, and (2867) Šteins. Pole and rotation information has been added for (2) Pallas and (21) Lutetia. Pole and rotation and mean radius information has been added for (1) Ceres. Pole information has been updated for (4) Vesta. The high precision realization for the pole and rotation rate of the Moon is updated. Alternative orientation models for Mars, Jupiter, and Saturn are noted. The Working Group also reaffirms that once an observable feature at a defined longitude is chosen, a longitude definition origin should not change except under unusual circumstances. It is also noted that alternative coordinate systems may exist for various (e.g. dynamical) purposes, but specific cartographic coordinate system information continues to be recommended for each body. The Working Group elaborates on its purpose, and also announces its plans to occasionally provide limited updates to its recommendations via its website, in order to address community needs for some updates more often than every 3 years. Brief recommendations are also made to the general

  1. The Brighton Collaboration Viral Vector Vaccines Safety Working Group (V3SWG).

    PubMed

    Chen, Robert T; Carbery, Baevin; Mac, Lisa; Berns, Kenneth I; Chapman, Louisa; Condit, Richard C; Excler, Jean-Louis; Gurwith, Marc; Hendry, Michael; Khan, Arifa S; Khuri-Bulos, Najwa; Klug, Bettina; Robertson, James S; Seligman, Stephen J; Sheets, Rebecca; Williamson, Anna-Lise

    2015-01-01

    Recombinant viral vectors provide an effective means for heterologous antigen expression in vivo and thus represent promising platforms for developing novel vaccines against human pathogens from Ebola to tuberculosis. An increasing number of candidate viral vector vaccines are entering human clinical trials. The Brighton Collaboration Viral Vector Vaccines Safety Working Group (V3SWG) was formed to improve our ability to anticipate potential safety issues and meaningfully assess or interpret safety data, thereby facilitating greater public acceptance when licensed.

  2. Process for forming shaped group III-V semiconductor nanocrystals, and product formed using process

    DOEpatents

    Alivisatos, A. Paul; Peng, Xiaogang; Manna, Liberato

    2001-01-01

    A process for the formation of shaped Group III-V semiconductor nanocrystals comprises contacting the semiconductor nanocrystal precursors with a liquid media comprising a binary mixture of phosphorus-containing organic surfactants capable of promoting the growth of either spherical semiconductor nanocrystals or rod-like semiconductor nanocrystals, whereby the shape of the semiconductor nanocrystals formed in said binary mixture of surfactants is controlled by adjusting the ratio of the surfactants in the binary mixture.

  3. Iii-V Compound Semiconductor Integrated Charge Storage Structures for Dynamic and Non-Volatile Memory Elements

    NASA Astrophysics Data System (ADS)

    Hetherington, Dale Laird

    This thesis presents an investigation into a novel group of GaAs charge storage devices. These devices, which are an integration of bipolar and junction field effect transistor structures were conceived, designed, fabricated, and tested within this study. The purpose was to analyse new types of charge storage devices, which are suitable for fabrication and lead to the development of dynamic and nonvolatile memories in III-V compound semiconductors. Currently, III-V semiconductor storage devices consist only of capacitors, where data is destroyed during reading and electrical erasure is difficult. In this work, four devices types were demonstrated that exhibit nondestructive reading, and three of the prototypes can be electrically erased. All types use the junction field effect transistor (JFET) for charge sensing, with each having different bipolar or epitaxial layer structure controlling the junction gate. The bottom epitaxial layer in each case served as the JFET channel. Two of the device types have three alternately doped layers, while the remaining two have four alternately doped layers. In all cases, removal of majority carriers from the middle layers constitutes stored charge. The missing carriers deplete the current carrying a region of the JFET channel. Drain current of the JFET becomes an indicator of stored charge. The basic function of each JFET memory element type is independent of interchanging n- and p- type doping within the structure type. Some performance advantage can be realized, however, by sensing with an n-type channel as compared to p- type due to increased carrier mobility. All device types exhibit storage time characteristics of order ten seconds. Devices are constructed in epitaxial layers grown by molecular beam epitaxy (MBE) reactors. The design of the epitaxial layers is an intrinsic part, together with the electrical design, of the storage device concept. These concepts are implemented first with photolithography masks which are used

  4. Finite Element Simulation of Machining of Ti6Al4V Alloy

    NASA Astrophysics Data System (ADS)

    Rizzuti, S.; Umbrello, D.

    2011-05-01

    Titanium and its alloys are an important class of materials, especially for aerospace applications, due to their excellent combination of strength and fracture toughness as well as low density. However, these materials are generally regarded as difficult to machine because of their low thermal conductivity and high chemical reactivity with cutting tool materials. Moreover, the low thermal conductivity of Titanium inhibits dissipation of heat within the workpiece causing an higher temperature at the cutting edge and generating for higher cutting speed a rapid chipping at the cutting edge which leads to catastrophic failure. In addition, chip morphology significantly influences the thermo-mechanical behaviour at the workpiece/tool interface, which also affects the tool life. In this paper a finite element analysis of machining of TiAl6V4 is presented. In particular, cutting force, chip morphology and segmentation are taken into account due to their predominant roles to determine machinability and tool wear during the machining of these alloys. Results in terms of residual stresses are also presented. Moreover, the numerical results are compared with experimental ones.

  5. JV Task 94 - Air Quality V: Mercury, Trace Elements, SO3, and Particulate Matter Conference

    SciTech Connect

    Thomas A. Erickson

    2007-01-31

    This final report summarizes the planning, preparation, facilitation and production, and summary of the conference entitled 'Air Quality V: Mercury, Trace Elements, SO{sub 3}, and Particulate Matter,' held September 18-21, 2005, in Arlington, Virginia. The goal of the conference was to build on the discussions of the first four Air Quality Conferences, providing further opportunity for leading representatives of industry, government, research institutions, academia, and environmental organizations to discuss the key interrelationships between policy and science shaping near-term regulations and controls and to assist in moving forward on emerging issues that will lead to acceptable programs and policies to protect human health, the environment, and economic growth. The conference was extremely timely, as it was the last large conference prior to publication of the U.S. Environmental Protection Agency's final regulations for mercury control from coal-fired utilities, and provided a forum to realistically assess the status of mercury controls in relation to the new regulations.

  6. Finite Element Simulation of Machining of Ti6Al4V Alloy

    SciTech Connect

    Rizzuti, S.; Umbrello, D.

    2011-05-04

    Titanium and its alloys are an important class of materials, especially for aerospace applications, due to their excellent combination of strength and fracture toughness as well as low density. However, these materials are generally regarded as difficult to machine because of their low thermal conductivity and high chemical reactivity with cutting tool materials. Moreover, the low thermal conductivity of Titanium inhibits dissipation of heat within the workpiece causing an higher temperature at the cutting edge and generating for higher cutting speed a rapid chipping at the cutting edge which leads to catastrophic failure. In addition, chip morphology significantly influences the thermo-mechanical behaviour at the workpiece/tool interface, which also affects the tool life.In this paper a finite element analysis of machining of TiAl6V4 is presented. In particular, cutting force, chip morphology and segmentation are taken into account due to their predominant roles to determine machinability and tool wear during the machining of these alloys. Results in terms of residual stresses are also presented. Moreover, the numerical results are compared with experimental ones.

  7. Architectural and Functional Diversity of Polycomb Group Response Elements in Drosophila

    PubMed Central

    Brown, J. Lesley; Kassis, Judith A.

    2013-01-01

    Polycomb group response elements (PREs) play an essential role in gene regulation by the Polycomb group (PcG) repressor proteins in Drosophila. PREs are required for the recruitment and maintenance of repression by the PcG proteins. PREs are made up of binding sites for multiple DNA-binding proteins, but it is still unclear what combination(s) of binding sites is required for PRE activity. Here we compare the binding sites and activities of two closely linked yet separable PREs of the Drosophila engrailed (en) gene, PRE1 and PRE2. Both PRE1 and PRE2 contain binding sites for multiple PRE–DNA-binding proteins, but the number, arrangement, and spacing of the sites differs between the two PREs. These differences have functional consequences. Both PRE1 and PRE2 mediate pairing-sensitive silencing of mini-white, a functional assay for PcG repression; however, PRE1 requires two binding sites for Pleiohomeotic (Pho), whereas PRE2 requires only one Pho-binding site for this activity. Furthermore, for full pairing-sensitive silencing activity, PRE1 requires an AT-rich region not found in PRE2. These two PREs behave differently in a PRE embryonic and larval reporter construct inserted at an identical location in the genome. Our data illustrate the diversity of architecture and function of PREs. PMID:23934890

  8. Elemental copper nanoparticle toxicity to different trophic groups involved in anaerobic and anoxic wastewater treatment processes.

    PubMed

    Gonzalez-Estrella, Jorge; Puyol, Daniel; Gallagher, Sara; Sierra-Alvarez, Reyes; Field, Jim A

    2015-04-15

    Elemental copper nanoparticles (Cu(0) NPs) are potentially inhibitory to the different key microbial trophic groups involved in biological wastewater treatment processes. Cu-based NPs are known to be toxic to methanogens at low concentrations. However, very little is known about the toxic effect of Cu(0) NPs on other microbial groups involved in either upper trophic levels of anaerobic digestion or anoxic nitrogen removal processes. This study evaluated the toxicity of Cu(0) NPs to glucose fermentation, syntrophic propionate oxidation and denitrification in shaken batch bioassays with soluble substrates. Batch experiments were also supplemented with CuCl2 to evaluate the inhibitory impact of soluble Cu(II) ions. Syntrophic propionate oxidation and glucose fermentation were the least and most inhibited processes with inhibition constant (Ki) values of 0.202 and 0.047 mM of added Cu(0) NPs, respectively. Further analyses revealed that the Ki values calculated as a function of the free soluble Cu concentration were <0.003 mM for every biological process tested and most of these Ki values were similar in order of magnitude regardless of whether the Cu source was CuCl2 or Cu(0) NPs. The results taken as a whole indicate that Cu(0) NPs are toxic to all the microbial processes studied. Therefore, Cu(0) NPs can potentially be an important inhibitor of anaerobic wastewater treatment processes that rely on these trophic groups. The evidence suggests that the inhibitory impact of Cu(0) NPs was mainly due to the release of toxic Cu(II) ions originating from the corrosion and dissolution of Cu(0) NPs.

  9. Next Generation Monolayer Structures of Group V Elements: Nitrogene and Antimonene

    NASA Astrophysics Data System (ADS)

    Ozcelik, Ongun; Akturk, Olcay; Durgun, Engin; Ciraci, Salim

    Based on first-principles density functional theory, we predict that nitrogen and antimony atoms can form single-layer, buckled honeycomb structures called nitrogene and antimonene, which are rigid and stable even above room temperature. The 2D crystalline phase of nitrogen, which corresponds to a local minimum in the Born-Oppenheimer surface, is a nonmagnetic insulator with saturated pi bonds. When grown on a substrate like Al(111) surface or graphene, nitrogene binds weakly to substrates and hence preserves its free-standing properties, but it can easily be pealed off. Zigzag and armchair nanoribbons have fundamental band gaps derived from reconstructed edge states. These band gaps are tunable with size and suitable for the emerging field of 2D electronics. Nitrogene and antimonene form not only bilayer, but also 3D graphitic multilayer structures. Single-layer nitrogene can nucleate and grow on the armchair edges of hexagonal boron nitride. Starting from the pseudo-layered character of 3D bulk crystals of antimony, we also demonstrate the formation of monolayer antimonene structure which is similar to nitrogene.

  10. Measurement of the mass attenuation coefficient from 81 keV to 1333 keV for elemental materials Al, Cu and Pb

    NASA Astrophysics Data System (ADS)

    Gjorgieva, Slavica; Barandovski, Lambe

    2016-03-01

    The mass attenuation coefficients (μ/ρ) for 3 high purity elemental materials Al, Cu and Pb were measured in the γ-ray energy range from 81 keV up to 1333 keV using 22Na, 60Co 133Ba and 133Cs as sources of gamma radiation. Well shielded detector (NaI (Tl) semiconductor detector) was used to measure the intensity of the transmitted beam. The measurements were made under condition of good geometry, assuring that any photon absorbed or deflected appreciably does not reach the detector. The measured values are compared with the theoretical ones obtained by Seltzer (1993).

  11. Environmental Vibrio spp., isolated in Mozambique, contain a polymorphic group of integrative conjugative elements and class 1 integrons.

    PubMed

    Taviani, Elisa; Ceccarelli, Daniela; Lazaro, Nivalda; Bani, Stefania; Cappuccinelli, Piero; Colwell, Rita R; Colombo, Mauro M

    2008-04-01

    Circulation of mobile genetic elements linked to drug resistance spread was studied in Vibrio strains isolated from surface urban water (river and sea) and shellfish samples in 2002-2003 in Maputo, Mozambique. Class 1 integrons and integrating conjugative elements (ICE) were investigated by PCR and mating experiments in strains of major health interest: 10 Vibrio cholerae, six Vibrio parahaemolyticus, two Vibrio alginolyticus and one Vibrio fluvialis. Resistance to at least two antibiotics (predominantly beta-lactams) was detected in all the strains, with additional resistances to sulfamethoxazole, spectinomycin, streptomycin and/or trimethoprim. Class 1 integrons contributed partially to the expression of drug resistance and were found in five isolates: four V. cholerae (blaP1 cassette, one strain also contained the dfrA15 cassette) and one V. alginolyticus (aadA2 cassette). ICEs, apparently devoid of resistance genes, were found in eight V. cholerae, three V. parahaemolyticus and one V. fluvialis isolates. A wide variability was observed by molecular characterization of ICEs. Five ICEs were included in the SXT/R391 family and seven ICEs were not classified. Our results indicate that the SXT/R391 family and related ICEs comprise a large class of polymorphic genetic elements widely circulating in environmental Vibrio strains in Africa, beside those evidently linked to drug resistance in clinical isolates.

  12. The compositional classification of chondrites. V - The Karoonda (CK) group of carbonaceous chondrites

    NASA Astrophysics Data System (ADS)

    Kallemeyn, G. W.; Rubin, A. E.; Wasson, J. T.

    1991-03-01

    In the Karoonda, or 'CK' group of carbonaceous chondrites, all normal members are metamorphosed and, while some contain shock veins, all exhibit various degrees of blackening due to fine sulfide and magnetite particle dispersions in silicates. The elemental abundance patterns in CK chondrites are similar to those in CO chondrites, and rather more similar to those in CV chondrites; CK refractory siderophile abundances are intermediate between CV and CO levels. The exceptional abundance of CK chondrites in Antarctica is accounted for in light of the fragmentation of the CK parent objects, which produced a greater proportion of small micrometeoroids.

  13. Report of the IAU Working Group on cartographic coordinates and rotational elements: 2009

    USGS Publications Warehouse

    Archinal, Brent A.; A’Hearn, Michael F.; Bowell, Edward; Conrad, Al; Consolmagno, Guy J.; Courtin, Regis; Fukushima, Toshio; Hestroffer, Daniel; Hilton, James L.; Krasinsky, Georgij A.; Neumann, Gregory; Oberst, Jurgen; Seidelmann, P. Kenneth; Stooke, Philip; Tholen, David J.; Thomas, Peter C.; Williams, Iwan P.

    2010-01-01

    Every three years the IAU Working Group on Cartographic Coordinates and Rotational Elements revises tables giving the directions of the poles of rotation and the prime meridians of the planets, satellites, minor planets, and comets. This report takes into account the IAU Working Group for Planetary System Nomenclature (WGPSN) and the IAU Committee on Small Body Nomenclature (CSBN) definition of dwarf planets, introduces improved values for the pole and rotation rate of Mercury, returns the rotation rate of Jupiter to a previous value, introduces improved values for the rotation of five satellites of Saturn, and adds the equatorial radius of the Sun for comparison. It also adds or updates size and shape information for the Earth, Mars’ satellites Deimos and Phobos, the four Galilean satellites of Jupiter, and 22 satellites of Saturn. Pole, rotation, and size information has been added for the asteroids (21) Lutetia, (511) Davida, and (2867) Šteins. Pole and rotation information has been added for (2) Pallas and (21) Lutetia. Pole and rotation and mean radius information has been added for (1) Ceres. Pole information has been updated for (4) Vesta. The high precision realization for the pole and rotation rate of the Moon is updated. Alternative orientation models for Mars, Jupiter, and Saturn are noted. The Working Group also reaffirms that once an observable feature at a defined longitude is chosen, a longitude definition origin should not change except under unusual circumstances. It is also noted that alternative coordinate systems may exist for various (e.g. dynamical) purposes, but specific cartographic coordinate system information continues to be recommended for each body. The Working Group elaborates on its purpose, and also announces its plans to occasionally provide limited updates to its recommendations via its website, in order to address community needs for some updates more often than every 3 years. Brief recommendations are also made to the

  14. [Affinity of the elements in group VI of the periodic table to tumors and organs].

    PubMed

    Ando, A; Hisada, K; Ando, I

    1976-10-01

    In order to investigate the tumor affinity radioisotopes, chromium (51Cr), molybdenum (99Mo), tungsten (181W), selenium (75Se) and tellurium (127mTe)--the elements of group VI in the periodic table--were examined, using the rats which were subcutaneously transplanted with Yoshida sarcoma. Seven preprarations, sodium chromate (Na251CrO4), chromium chloride (51CrCl3), normal ammonium molybdate ((NH4)299MoO7), sodium tungstate (Na2181WO4), sodium selenate (Na275SeO4), sodium selenite (Na275SeO3) and tellurous acid (H2127mTeO3) were injected intravenously to each group of tumor bearing rats. These rats were sacrificed at various periods after injection of each preparation: 3 hours, 24 hours and 48 hours in all preparations. The radioactivities of the tumor, blood, muscle, liver, kidney and spleen were measured by a well-type scintillation counter, and retention values (in every tissue including the tumor) were calculated in percent of administered dose per g-tissue weight. All of seven preparations did not have any affinity for malignant tumor. Na251CrO4 and H2127mTeO3 had some affinity for the kidneys, and Na275SeO3 had some affinity for the liver. Na2181WO4 and (NH4)299MoO4 disappeared very rapidly from the blood and soft tissue, and about seventy-five percent of radioactivity was excreted in urine within first 3 hours.

  15. The nature of the interaction of dimethylselenide with IIIA group element compounds.

    PubMed

    Madzhidov, Timur I; Chmutova, Galina A

    2013-05-16

    The first systematic theoretical study of the nature of intermolecular bonding of dimethylselenide as donor and IIIA group element halides as acceptors was made with the help of the approach of Quantum Theory of Atoms in Molecules. Density Functional Theory with "old" Sapporo triple-ζ basis sets was used to calculate geometry, thermodynamics, and wave function of Me2Se···AX3 complexes. The analysis of the electron density distribution and the Laplacian of the electron density allowed us to reveal and explain the tendencies in the influence of the central atom (A = B, Al, Ga, In) and halogen (X = F, Cl, Br, I) on the nature of Se···A bonding. Significant changes in properties of the selenium lone pair upon complexation were described by means of the analysis of the Laplacian of the charge density. Charge transfer characteristics and the contributions to it from electron localization and delocalization were analyzed in terms of localization and delocalization indexes. Common features of the complexation and differences in the nature of bonding were revealed. Performed analysis evidenced that gallium and indium halide complexes can be attributed to charge transfer-driven complexes; aluminum halides complexes seem to be mainly of an electrostatic nature. The nature of bonding in different boron halides essentially varies; these complexes are stabilized mainly by covalent Se···B interaction. In all the complexes under study covalence of the Se···A interaction is rather high.

  16. Platinum group element incorporation into human bones resulting from increased anthropogenic utilization

    NASA Astrophysics Data System (ADS)

    Darrah, T. H.; Hannigan, R. E.; Campbell, E.; Prutsman-Pfeiffer, J.

    2009-12-01

    Platinum group elements (including Pt, Pd, Ru, Rh, Os, Ir) are rare precious metals that occur at exceedingly low concentrations in the Earth’s crust (~0.02-0.5 ng/g). Utilization of PGEs in the catalytic converter of automobiles, medical treatments, electronics, and as a catalyst, has rapidly increased since the early 20th century, leading to increased anthropogenic PGE emissions and consequently increasing concentrations in the environment. Recent reports indicate that environmental PGE concentrations are increasing in urban air, roadside soils, and aquatic environments (Rauch and Morrison, 2008). As a result, there is an increased potential for PGE uptake into the biosphere. To evaluate bio-incorporation of PGEs into the human body we use ICP-MS to analyze for PGE concentration in human bones. Human bone minerals serve as a reservoir for the majority of the body’s trace metals and provide a measure of PGE incorporation into the human body from various environmental sources. We compare PGE concentrations in femoral heads of 30 present-day modern humans to those in femurs of 10 humans exhumed from 18th and 19th century burial sites, whose metal exposures predate extensive anthropogenic use of PGEs.

  17. Improved and Expanded Near-IR Oscillator Strengths for Fe-group Elements

    NASA Astrophysics Data System (ADS)

    Wood, Michael P.; Nave, Gillian

    2015-01-01

    The use of modern experimental techniques, including LIF lifetime and FTS branching fraction measurements, has significantly increased the scope and reliability of laboratory atomic transition probabilities in the UV and visible. However, the combination of these techniques is problematic in the IR, a region of increasing importance due to improved detector, spectrometer, and telescope technologies. The result is a significant gap between the capabilities to record new IR astronomical spectra and the data needed to sufficiently understand and analyze them. To aid in closing this gap, we are developing new laboratory techniques to measure improved and expanded sets of oscillator strengths in the near-IR (λ ≈ 1-5 μm), with a primary focus on the Fe-group elements. A description of the methods proposed and their applicability will be presented. Input from the astronomical community is essential in order to focus the research on those lines and atomic species representing the greatest near-IR atomic data needs.

  18. Structure and magnetism in novel group IV element-based magnetic materials

    SciTech Connect

    Tsui, Frank

    2013-08-14

    The project is to investigate structure, magnetism and spin dependent states of novel group IV element-based magnetic thin films and heterostructures as a function of composition and epitaxial constraints. The materials systems of interest are Si-compatible epitaxial films and heterostructures of Si/Ge-based magnetic ternary alloys grown by non-equilibrium molecular beam epitaxy (MBE) techniques, specifically doped magnetic semiconductors (DMS) and half-metallic Heusler alloys. Systematic structural, chemical, magnetic, and electrical measurements are carried out, using x-ray microbeam techniques, magnetotunneling spectroscopy and microscopy, and magnetotransport. The work is aimed at elucidating the nature and interplay between structure, chemical order, magnetism, and spin-dependent states in these novel materials, at developing materials and techniques to realize and control fully spin polarized states, and at exploring fundamental processes that stabilize the epitaxial magnetic nanostructures and control the electronic and magnetic states in these complex materials. Combinatorial approach provides the means for the systematic studies, and the complex nature of the work necessitates this approach.

  19. Characterization of Group V Dubnium Homologs on DGA Extraction Chromatography Resin from Nitric and Hydrofluoric Acid Matrices

    SciTech Connect

    Despotopulos, J D; Sudowe, R

    2012-02-21

    analytes based on steric interactions between the cavity of the crown ether and electrostatic interactions between the oxygen's of the ether and cations in the mobile phase. This particular resin has been shown to have an extremely high uptake affinity for Pb, a direct homolog of element 114, and is thus a good initial extractant to examine for a potential element 114 chemical system. Figure 1.1 shows the respective extractant molecules from the DGA and Pb resins. Batch uptake experiments were conducted to examine the uptake behavior of Ta on the DGA resin. Batch uptake experiments were also conducted to examine the uptake behavior of Ge on the Pb resin. Column experiments were designed based on batch uptake experiments of Ta, Am, Pa, Np, Zr, and Nb to establish a sequential extraction of Group IV/V homologs as well as Am for potential use as a Db chemical system.

  20. Re-187-Os-187, Pt-190-Os-186 Isotopic and Highly Siderophile Element Systematics of Group IVA Irons

    NASA Technical Reports Server (NTRS)

    Walker, R. J.; McCoy, T. J.; Schulte, R. F.; McDonough, W. F.; Ash, R. D.

    2005-01-01

    We have recently completed Re-187-Os-187 and Pt-190-Os-186 isotopic and elemental studies of the two largest magmatic iron meteorite groups, IIAB and IIIAB [1]. These studies revealed closed-system behavior of both isotopic systems, but complex trace element behavior for Re, Pt and Os in group IIIAB. Here we examine isotopic and trace elemental systematics of group IVA irons. The IVA irons are not as extensively fractionated as IIAB and IIIAB and their apparently less complex crystallization history may make for more robust interpretation of the relative partitioning behavior of Re, Pt and Os, as well as the other highly siderophile elements (HSE) measured here; Pd, Ru and Ir [e.g. 2]. An additional goal of our continuing research plan for iron meteorites is to assess the possibility of relating certain ungrouped irons with major groups via trace element modeling. Here, the isotopic and trace element systematics of the ungrouped irons Nedagolla and EET 83230 are compared with the IVA irons.

  1. Synthesis and properties of layered synthetic microstructure (LSM) dispersion elements for 62 eV (200A) to 1. 24 keV (10A) radiation. Final report

    SciTech Connect

    Barbee, T.W. Jr.

    1981-08-01

    The opportunities offered by engineered synthetic multilayer dispersion elements for x-rays have been recognized since the earliest days of x-ray diffraction analysis. In this paper, application of sputter deposition technology to the synthesis of Layered Synthetic Microstructure (LSMs) of sufficient quality for use as x-ray dispersion elements is discussed. It will be shown that high efficiency, controllable bandwidth dispersion elements, with d spacings varying from 15 A to 180 A, may be synthesized onto both mechanically stiff and flexible substrates. Multilayer component materials include tungsten, niobium, molybdenum, titanium, vanadium, and silicon layers separated by carbon layers. Experimental observations of peak reflectivity in first order, integrated reflectivity in first order, and diffraction performance at selected photon energies in the range, 100 to 15,000 eV, will be reported and compared to theory.

  2. Terahertz lasers based on intracentre transitions of group V donors in uniaxially deformed silicon

    SciTech Connect

    Kovalevsky, K A; Zhukavin, R Kh; Tsyplenkov, V V; Shastin, V N; Abrosimov, N V; Pavlov, S G; Hübers, H W

    2015-02-28

    This paper presents a brief overview of available experimental data on the characteristics of stimulated terahertz emission (4.9 – 6.4 THz) from optically excited neutral group V donors (phosphorus, antimony, arsenic and bismuth) in crystalline silicon subjected to uniaxially compressive strain along the [100] axis. Strain is shown to have a significant effect on the characteristics in question. Optimal strain depends on the dopant and may reduce the threshold pump intensity and improve lasing efficiency. We discuss possible mechanisms behind this effect and estimate the limiting output emission parameters. (terahertz radiation)

  3. On-line gas phase chromatography of the bromides of the group 4, 5, and 6 elements

    SciTech Connect

    Sylwester, E.R.; Gregorich, K.E.; Lee, D.M.; Chung, Y.H.

    1997-12-31

    Gas phase chromatography has been used to determine the volatility of bromides of the group 4, 5, and 6 elements, including the transactinides 104 (Rf) and 105 (Ha). The Heavy Element Volatility Instrument (HEVI) was used to measure the volatilities of the bromides of short-lived isotopes of these elements. Adsorption enthalpy values were calculated from the observed volatilities using a Monte Carlo program. The values for RfBr{sub 4} and HaBr{sub 5} are similar to ZrBr{sub 4} and NbBr{sub 5} rather than to HfBr{sub 4} and TaBr{sub 5}. This deviates from a simple extrapolation from periodic table trends and may indicate the influence of relativistic effects on the electronic level structure of these transactinides. The group 6 element Seaborgium (Sg) has not yet been studied due to the low production cross-section.

  4. Premcor Refining Group, Port Arthur, Texas; Petition to Object to Title V Operating Permit

    EPA Pesticide Factsheets

    This document may be of assistance in applying the Title V air operating permit regulations. This document is part of the Title V Petition Database available at www2.epa.gov/title-v-operating-permits/title-v-petition-database.

  5. Comparison between steady-state and dynamic I-V measurements from a single-cell thermionic fuel element

    SciTech Connect

    Wernsman, B.

    1997-01-01

    A comparison between steady-state and dynamic I-V measurements from a single-cell thermionic fuel element (TFE) is made. The single-cell TFE used in this study is the prototype for the 40kW{sub e} space nuclear power system that is similar to the 6kW{sub e} TOPAZ-II. The steady-state I-V measurements influence the emitter temperature due to electron cooling. Therefore, to eliminate the steady-state I-V measurement influence on the TFE and provide a better understanding of the behavior of the thermionic energy converter and TFE characteristics, dynamic I-V measurements are made. The dynamic I-V measurements are made at various input power levels, cesium pressures, collector temperatures, and steady-state current levels. From these measurements, it is shown that the dynamic I-V{close_quote}s do not change the TFE characteristics at a given operating point. Also, the evaluation of the collector work function from the dynamic I-V measurements shows that the collector optimization is not due to a minimum in the collector work function but due to an emission optimization. Since the dynamic I-V measurements do not influence the TFE characteristics, it is believed that these measurements can be done at a system level to understand the influence of TFE placement in the reactor as a function of the core thermal distribution. {copyright} {ital 1997 American Institute of Physics.}

  6. Comparison between steady-state and dynamic I-V measurements from a single-cell thermionic fuel element

    SciTech Connect

    Wernsman, Bernard

    1997-01-10

    A comparison between steady-state and dynamic I-V measurements from a single-cell thermionic fuel element (TFE) is made. The single-cell TFE used in this study is the prototype for the 40 kW{sub e} space nuclear power system that is similar to the 6 kW{sub e} TOPAZ-II. The steady-state I-V measurements influence the emitter temperature due to electron cooling. Therefore, to eliminate the steady-state I-V measurement influence on the TFE and provide a better understanding of the behavior of the thermionic energy converter and TFE characteristics, dynamic I-V measurements are made. The dynamic I-V measurements are made at various input power levels, cesium pressures, collector temperatures, and steady-state current levels. From these measurements, it is shown that the dynamic I-V's do not change the TFE characteristics at a given operating point. Also, the evaluation of the collector work function from the dynamic I-V measurements shows that the collector optimization is not due to a minimum in the collector work function but due to an emission optimization. Since the dynamic I-V measurements do not influence the TFE characteristics, it is believed that these measurements can be done at a system level to understand the influence of TFE placement in the reactor as a function of the core thermal distribution.

  7. Cipollone v. Liggett Group, Inc. strengthens federal preemption defense in pesticide tort litigation

    SciTech Connect

    Stevens, R.W.

    1993-12-31

    When the United States Supreme Court held that the Federal Cigarette Labeling and Advertising Act (Cigarette Act) of 1969 preempted plaintiff`s failure to warn claims in Cipollone v. Liggett Group, Inc., the decision directly affected a far wider range of product liability cases than those involving only cigarettes. This article analyzes how Cipollone affects the defense raised in pesticide injury cases that the Federal Insecticide, Fungicide and Rodenticide Act (FIFRA) preempts state common law failure to warn claims. The Eleventh Circuit in Papas v. Upjohn Co. (Papas I), declining to follow contrary authority, held that FIFRA impliedly preempted state law claims that pesticides were inadequately labeled. On a petition for certiorari, the Supreme Court remanded the case back to the Eleventh Circuit for reconsideration in light of Cipollone. Recently, the Eleventh Circuit in Papas v. Upjohn Co. (Papas II) applied Cipollone to hold that FIFRA expressly preempts the state law claims. This article argues that Papas II correctly held, after Cipollone, that FIFRA preempts the state inadequate labeling and failure to warn claims in pesticide cases. 86 refs.

  8. [Migration and transformation of anthropogenic platinum group elements in environment: a review].

    PubMed

    Li, Pei-Miao; Gao, Xue-Lu

    2012-12-01

    Anthropogenic platinum group elements (PGEs) are widely applied in vehicle exhaust catalytic converters (VECs), industrial catalysts, and pharmaceutics, making the PGEs, especially Pt, Pd, and Rh, become the newly environmental pollutants in some fields. Given the positive correlations between the Pt/Pd and Pt/Rh ratios in various environmental samples and the active components of VECs, the VECs containing PGEs as catalysts are regarded as the primary source of PGEs pollution. Sufficient reports indicated that in the past three decades, there was a significant increase of PGEs concentrations in diverse environmental matrices like airborne particulate matters, aquatic ecosystem components (e.g., river water, rain water, groundwater, seawater, and sediments), soils, road dusts, and organisms. It was generally assumed that anthropogenic PGEs behave in inert manner, and the health risks associated with the environmental exposures to PGEs are minimal. However, the recent studies on PGEs toxicity and environmental bioavailability indicated that once entering environment, anthropogenic PGEs might easily be mobilized and transformed into more toxic forms under the actions of various biogeochemical processes, and thereby, enhanced their bioavailability and posed potential health risks to human beings through food chain. This paper summarized the research results about the sources, distribution, and biogeochemical behaviors of PGEs in various environmental media, and it was considered that to establish the standards of PGEs for human health risks, to develop standard substances of PGEs for environmental measurements, to study the PGEs in the sediments of marginal seas, and to assess the toxicity of PGEs to marine mollusks, the present contamination status of PGEs in foods, and the risks of PGEs to human health would be the hot research topics in the future.

  9. Complex anthropogenic sources of platinum group elements in aerosols on Cape Cod, USA.

    PubMed

    Sen, Indra S; Peucker-Ehrenbrink, Bernhard; Geboy, Nicholas

    2013-09-17

    Platinum group elements (PGE) of anthropogenic origin have been reported in rainwater, snow, roadside soil and vegetation, industrial waste, and urban airborne particles around the world. As recent studies have shown that PGE are bioavailable in the environment and pose health risks at chronic levels, the extent of PGE pollution is of global concern. In this study, we report PGE concentrations and osmium isotope ((187)Os/(188)Os) ratios of airborne particles (particulate matter, PM10) collected in Woods Hole, a small coastal village on Cape Cod, Massachusetts, U.S.A. The sampling site is more than 100 km away from the nearest urban centers (Boston, Providence) and has no large industrial emission center within a 30 km radius. The study reveals that, although PGE concentrations in rural airborne particulate matter are orders of magnitude lower than in urban aerosols, 69% of the total osmium is of anthropogenic origin. Anthropogenic PGE signatures in airborne particles are thus not restricted to large cities with high traffic flows and substantial industries; they can also be found in rural environments. We further conclude that the combination of Pt/Rh concentration ratios and (187)Os/(188)Os composition can be used to trace PGE sources. The Pt/Rh and (187)Os/(188)Os composition of Woods Hole aerosols indicate that the anthropogenic PGE fraction is primarily sourced from ore smelting processes, with possible minor contributions from fossil fuel burning and automobile catalyst-derived materials. Our results further substantiate the use of (187)Os/(188)Os in source apportionment studies on continental scales.

  10. The ratios of emission probabilities of Auger electrons for 3d transition elements at 59,5 keV

    NASA Astrophysics Data System (ADS)

    Kündeyi, Kadriye; Aylıkcı, Nuray Küp; Tıraşoǧlu, Engin; Kahoul, Abdelhalim; Aylıkcı, Volkan

    2017-02-01

    The ratios of emission probabilities were determined by using the measured K shell X-ray intensity ratio values for elements from Sc to Zn. For the experimental measurements, the samples were excited by 59.5 keV γ rays from a 241Am annular radioactive source. The emitted K X-rays from the samples were counted by an Ultra-LEGe detector with a resolution of 150 eV at 5.9 keV. The ratios of emission probabilities were denoted as uand v which means p(KLX)/p(KLL) and p(KXY)/p(KLL) respectively. The extracted values from the measured intensity ratios and calculated intensity ratios were compared with the earlier studies. It was found that the ratios of emission probabilities that evaluated from the calculated intensity ratios were agree well with the earlier studies except for Zn.

  11. Structure and optical properties of evaporated films of the Cr- and V-group metals

    NASA Technical Reports Server (NTRS)

    Nestell, J. E., Jr.; Christy, R. W.; Cohen, M. H.; Ruben, G. C.

    1980-01-01

    Thin films of Cr, Mo, and W rapidly evaporated in high vacuum (5 x 10 to the -7th torr) onto room-temperature substrates show anomalously low reflectance (compared to bulk samples). From electron and X-ray diffraction and electron microscopy, the normal bcc crystal structure is found, but with very fine grains. Columnar grains about 100 A in diameter were separated by a less dense grain-boundary network about 10-A wide. The measured optical conductivity agrees with an inhomogeneous-medium model that assumes the normal crystalline conductivity for the grain interiors, with model parameters that correlate to the observed columnar grain size. In contrast, V and Nb films rapidly evaporated onto room-temperature substrates have the reflectance of bulk crystalline material. On liquid-nitrogen temperature substrates, however, V and Nb have normal bcc crystal structure but with small flat-plate grains, and the same model, with appropriate parameters, accounts for the optical conductivity. The difference between these two groups apparently depends on residual gases segregated at the grain boundaries in the Cr-group films.

  12. Validation of new superheavy elements and IUPAC-IUPAP joint working group

    NASA Astrophysics Data System (ADS)

    Jarlskog, Cecilia

    2016-12-01

    The great chemist Glenn Seaborg has written a delightful little book "Man-made Transuranium Elements", published in 1963, in which he points out that: "The former basic criterion for the discovery of a new element - namely, chemical identification and separation from all previously-known elements - had to be changed in the case of lawrencium (element 103). This also may be true for elements beyond lawrencium." Indeed this is what has happened. The elements with Z ≥ 103 are produced in nuclear reactions and are detected by counters. The detectors have undergone substantial refinement. For example one uses multiwire proportional chambers [for which George Charpak received the 1992 Nobel Prize in Physics] as well as solid state micro-strip detectors. In spite of this remarkable shift from chemistry to physics, the managerial staff of the International Union of Pure and Applied Chemistry (IUPAC) does not seem to be aware of what has been going on. The validation of superheavy elements should be done by physicists as the chemists lack the relevant competence as I will discuss here below. This article is about a collaboration between International Union of Pure and Applied Chemistry (IUPAC) and its sister organization International Union of Pure and Applied Physics (IUPAP), to deal with discovery of superheavy elements beyond Z = 112. I spent a great deal of time on this issue. In my opinion, the collaboration turned out to be a failure. For the sake of science, which should be our most important concern (and not politics), the rules for the future collaborations, if any, should be accurately defined and respected. The validation of new elements should be done by people who have the relevant competence - the physicists.

  13. An element-free Galerkin (EFG) method for numerical solution of the coupled Schrödinger-KdV equations

    NASA Astrophysics Data System (ADS)

    Liu, Yong-Qing; Cheng, Rong-Jun; Ge, Hong-Xia

    2013-10-01

    The present paper deals with the numerical solution of the coupled Schrödinger-KdV equations using the element-free Galerkin (EFG) method which is based on the moving least-square approximation. Instead of traditional mesh oriented methods such as the finite difference method (FDM) and the finite element method (FEM), this method needs only scattered nodes in the domain. For this scheme, a variational method is used to obtain discrete equations and the essential boundary conditions are enforced by the penalty method. In numerical experiments, the results are presented and compared with the findings of the finite element method, the radial basis functions method, and an analytical solution to confirm the good accuracy of the presented scheme.

  14. Trace-element concentrations in blood samples from welders of stainless steel or aluminium and a reference group.

    PubMed

    Ulfvarson, U; Wold, S

    1977-12-01

    The concentrations of 17 trace elements (e.g., copper, cobalt, iron, manganese, chromium, silicon and magnesium) were determined in whole blood samples of 81 persons working with different welding methods on stainless steel or aluminium and 68 nonwelders. Inorganic spark source mass spectrometry was used for the chemical analyses. The data were analyzed by the SIMCA method for pattern recognition (discriminant analysis). No differences were found between the five groups, either in the average levels of the trace elements or in the correlation structures between the trace elements. Thus no blood concentration data on the analyzed elements and collected from a single person contained any information with respect to exposure to the welding fumes investigated.

  15. Theoretical predictions of properties and gas-phase chromatography behaviour of carbonyl complexes of group-6 elements Cr, Mo, W, and element 106, Sg

    NASA Astrophysics Data System (ADS)

    Pershina, V.; Anton, J.

    2013-05-01

    Fully relativistic, four-component density functional theory electronic structure calculations were performed for M(CO)6 of group-6 elements Cr, Mo, W, and element 106, Sg, with an aim to predict their adsorption behaviour in the gas-phase chromatography experiments. It was shown that seaborgium hexacarbonyl has a longer M-CO bond, smaller ionization potential, and larger polarizability than the other group-6 molecules. This is explained by the increasing relativistic expansion and destabilization of the (n - 1)d AOs with increasing Z in the group. Using results of the calculations, adsorption enthalpies of the group-6 hexacarbonyls on a quartz surface were predicted via a model of physisorption. According to the results, -ΔHads should decrease from Mo to W, while it should be almost equal - within the experimental error bars - for W and Sg. Thus, we expect that in the future gas-phase chromatography experiments it will be almost impossible - what concerns ΔHads - to distinguish between the W and Sg hexacarbonyls by their deposition on quartz.

  16. Theoretical predictions of properties and gas-phase chromatography behaviour of carbonyl complexes of group-6 elements Cr, Mo, W, and element 106, Sg.

    PubMed

    Pershina, V; Anton, J

    2013-05-07

    Fully relativistic, four-component density functional theory electronic structure calculations were performed for M(CO)6 of group-6 elements Cr, Mo, W, and element 106, Sg, with an aim to predict their adsorption behaviour in the gas-phase chromatography experiments. It was shown that seaborgium hexacarbonyl has a longer M-CO bond, smaller ionization potential, and larger polarizability than the other group-6 molecules. This is explained by the increasing relativistic expansion and destabilization of the (n - 1)d AOs with increasing Z in the group. Using results of the calculations, adsorption enthalpies of the group-6 hexacarbonyls on a quartz surface were predicted via a model of physisorption. According to the results, -ΔHads should decrease from Mo to W, while it should be almost equal--within the experimental error bars--for W and Sg. Thus, we expect that in the future gas-phase chromatography experiments it will be almost impossible--what concerns ΔHads--to distinguish between the W and Sg hexacarbonyls by their deposition on quartz.

  17. Labile trace elements in basaltic achondrites: Can they distinguish between meteorites from the Moon, Mars, and V-type asteroids?

    NASA Astrophysics Data System (ADS)

    Wolf, Stephen F.; Wang, Ming-Sheng; Lipschutz, Michael E.

    2009-06-01

    We report data for 14 mainly labile trace elements (Ag, Au, Bi, Cd, Cs, Ga, In, Rb, Sb, Se, Te, Tl, U, and Zn) in eight whole-rock lunar meteorites (Asuka [A-] 881757, Dar al Gani [DaG] 262, Elephant Moraine [EET] 87521, Queen Alexandra Range [QUE] 93069, QUE 94269, QUE 94281, Yamato [Y-] 793169, and Y-981031), and Martian meteorite (DaG 476) and incorporate these into a comparative study of basaltic meteorites from the Moon, Mars, and V-type asteroids. Multivariate cluster analysis of data for these elements in 14 lunar, 13 Martian, and 34 howardite, eucrite, and diogenite (HED) meteorites demonstrate that materials from these three parents are distinguishable using these markers of late, low-temperature episodes. This distinguishability is essentially as complete as that based on markers of high-temperature igneous processes. Concentrations of these elements in 14 lunar meteorites are essentially lognormally distributed and generally more homogeneous than in Martian and HED meteorites. Mean siderophile and labile element concentrations in the 14 lunar meteorites indicate the presence of a CI-equivalent micrometeorite admixture of 2.6% When only feldspathic samples are considered, our data show a slightly higher value of 3.4% consistent with an increasing micrometeorite content in regolith samples of higher maturity. Concentrations of labile elements in the 8 feldspathic samples hint at the presence of a fractionated highly labile element component, possibly volcanic in origin, at a level comparable to the micrometeorite component. Apparently, the process(es) that contributed to establishing lunar meteorite siderophile and labile trace element contents occurred in a system open to highly labile element transport.

  18. 76 FR 45248 - PJM Interconnection, L.L.C., PJM Power Providers Group v. PJM Interconnection, L.L.C...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-28

    ... Energy Regulatory Commission PJM Interconnection, L.L.C., PJM Power Providers Group v. PJM... Load Group, PJM Power Providers Group, and PSEG Companies. All interested parties are invited to attend... provides technical support for the free webcasts. It also offers access to this event via television in...

  19. ROLE OF SURFACE FUNCTIONAL GROUPS IN THE CAPTURE OF ELEMENTAL MERCURY AND MERCURIC CHLORIDE BY ACTIVATED CARBONS

    EPA Science Inventory

    The paper discusses using a laboratory-scale, fixed bed apparatus to study the role of surface functional groups (SFGs) in the capture of mercuric chloride (HgC12) and elemental mercury (Hgo) in nitrogen (N2) prior to flue gas atmosphere studies. The study focused on two activat...

  20. Hybrid in situ replacement for Samson group V Staphylococcus aureus aortic graft infection

    PubMed Central

    Karpenko, A A; Ignatenko, P V; Beliaev, A M

    2013-01-01

    Aortic prosthesis replacements including extra-anatomical bypass procedures, in situ revascularisations with the neoaortoiliac system, antibiotic bounded prostheses or allogeneic grafts have high graft reinfection rates. We described a case of a 68-year-old man with Samson group V Staphylococcus aureus infection of his aortobifemoral graft. He underwent an explantation of the infected graft, wound debridement and a hybrid in situ allogeneic aortoiliofemoral replacement. During surgery one of the limbs of the cryopreserved human aortic allogeneic graft was anastomosed with the endarterectomised left common iliac artery, which later was angioplastied and stented. The closed system Jackson-Pratt drains were used to prevent perigraft fluid collection. The groin wound was treated with the vacuum-assisted closure dressing. On review in 6 months he remained symptom free. We conclude that a hybrid management of infected aortic prosthesis may reduce graft reinfection. PMID:23897382

  1. Phase transitions in Group III-V and II-VI semiconductors at high pressure

    NASA Technical Reports Server (NTRS)

    Yu, S. C.; Liu, C. Y.; Spain, I. L.; Skelton, E. F.

    1979-01-01

    The structures and transition pressures of Group III-V and II-VI semiconductors and of a pseudobinary system (Ga/x/In/1-x/Sb) have been investigated. Results indicate that GaP, InSb, GaSb, GaAs and possible AlP assume Metallic structures at high pressures; a tetragonal, beta-Sn-like structure is adopted by only InSb and GaSb. The rocksalt phase is preferred in InP, InAs, AlSb, ZnO and ZnS. The model of Van Vechten (1973) gives transition pressures which are in good agreement with measured values, but must be refined to account for the occurrence of the ionic rocksalt structure in some compounds. In addition, discrepancies between the theoretical scaling values for volume changes at the semiconductor-to-metal transitions are observed.

  2. Strain induced topological phase transitions in monolayer honeycomb structures of group-V binary compounds

    PubMed Central

    Nie, Yaozhuang; Rahman, Mavlanjan; Wang, Daowei; Wang, Can; Guo, Guanghua

    2015-01-01

    We present first-principles calculations of electronic structures of a class of two-dimensional (2D) honeycomb structures of group-V binary compounds. Our results show these new 2D materials are stable semiconductors with direct or indirect band gaps. The band gap can be tuned by applying lattice strain. During their stretchable regime, they all exhibit metal-indirect gap semiconductor-direct gap semiconductor-topological insulator (TI) transitions with increasing strain from negative (compressive) to positive (tensile) values. The topological phase transition results from the band inversion at the Γ point which is due to the evolution of bonding and anti-bonding states under lattice strain. PMID:26656257

  3. Transposon telomeres are widely distributed in the Drosophila genus: TART elements in the virilis group

    PubMed Central

    Casacuberta, Elena; Pardue, Mary-Lou

    2003-01-01

    Telomeres of most animals, plants, and unicellular eukaryotes are made up of tandem arrays of repeated DNA sequences produced by the enzyme telomerase. Drosophila melanogaster has an unusual variation on this theme; telomeres consist of tandem arrays of sequences produced by successive transpositions of two non-LTR retrotransposons, HeT-A and TART. To explore the phylogenetic distribution of these variant telomeres, we have looked for TART homologues in a distantly related Drosophila species, virilis. We have found elements that, despite many differences in nucleotide sequence, retain significant amino acid similarity to TART from D. melanogaster. These D. virilis TART elements have features that characterize TART elements in D. melanogaster: (i) they are found in tandem arrays on chromosome ends, (ii) they are not found in euchromatin, and (iii) they produce both sense and antisense transcripts, with the antisense RNA being in excess. The D. virilis TART elements have one surprising feature: both of the ORFs contain long stretches of the trinucleotide repeat CAX, encoding polyglutamine (with a few interspersed histidines). These long polyglutamine stretches are conserved in the three D. virilis elements sequenced. They do not interrupt any domains of known function in the TART proteins and are not seen in TART proteins from other species. Comparison of the D. virilis and D. melanogaster telomeres suggests that the retrotransposon mechanism of telomere maintenance may have arisen before the separation of the genus Drosophila. PMID:12626755

  4. Simulation of nanoindentation experiment on RF magnetron sputtered nanocolumnar V2O5 film using finite element method

    NASA Astrophysics Data System (ADS)

    Porwal, Deeksha; Gupta, A. K.; Pillai, Anju M.; Sharma, Anand Kumar; Mukhopadhyay, Anoop Kumar; Khan, Kallol; Dey, Arjun

    2016-07-01

    The present work reports the nanomechanical behavior of a pulsed radio frequency (RF) magnetron sputtered vanadium pentoxide (V2O5) film deposited on silicon (Si) substrate using a combination of nanoindentation experiments and a finite element model (FEM). Deposited V2O5 film is characterized by x-ray diffraction (XRD), nanoprofilometry, field emission scanning electron microscopy (FESEM), nanoindentation and FEM. The phase pure 6.16 μm V2O5 film shows a nanocolumnar structure. The film exhibits nanohardness (H) of 0.16 ± 0.013 GPa and Young’s modulus (E) of about 12.05 ± 1.41 GPa. The FEM reproduces experimentally obtained load versus depth (P-h) plot and subsequently give yield stress and strain hardening component data of V2O5 film on Si substrate. Stress-strain behavior and von-Mises stress distribution of the V2O5 film with Si substrate system are also simulated. The FE model confirms the local maximum equivalent stress active underneath the nanoindenters to be nearly twice as high as the yield stress and thereby explains the plastic deformation observed in the V2O5 film.

  5. Oxidized As (V) in fore-arc mantle serpentinites: Transfer of fluid-soluble elements from slabs to arc magmas

    NASA Astrophysics Data System (ADS)

    Hattori, K. H.; Takahashi, Y.; Guillot, S.; Johanson, B.

    2004-12-01

    Fluids released from subducting slabs and sediments hydrate the overlying peridotites in mantle wedges. Such hydrated peridotites (serpentinites) are enriched in fluid-soluble elements, although insoluble elements show the refractory geochemical signature. The enrichment pattern of serpentinites is similar to that of arc magmas (Hattori & Guillot, 2003 in Geology). Arsenic is one of the most enriched soluble elements, reaching greater than 1000 times of the primitive mantle value. We examined the speciation and occurrence of As in serpentinites to understand how such a highly mobile element can be transferred from subducting slabs to arc magmas via mantle wedges. Our study used serpentinites associated with the Tso Morari eclogitic rocks in the Indus Suture Zone of Himalaya. They represent the hydrated peridotites at the base of mantle wedge beneath the margin of Eurasia and were exhumed from the depth of about 100 km during the active subduction of the Indian continental margin. The serpentinites are made up of antigorite, chromite, minor talc. It contains As ranging from 6 to 275 ppm and S up to 51 ppm, but most have S below detection limit, 4 ppm. X-ray absorption spectroscopy data show that As is mostly As(V) and combined with oxygen, although Minute grains of As-bearing sulphides and arsenides are identified in samples. The fractions of As(V), calculated from the X-ray absorption near-edge structure, are greater in samples with higher As contents. High proportion of As(V) in the fore-arc mantle serpentinites contasts with high As(III) in the serpentinite at the base of the Nidar ophiolite. The source of As (V) in the serpentinites is most likely As adsorped on Fe- and Mn-oxides in subducted sediments and slabs. It was released during the subduction of slab and sediments at low temperatures, \\< 350° C, and shallow depths, \\< 25 km. Continuous flux of water from slabs at the base of the mantle wedge likely maintained As in oxidized condition. Arsenic in the

  6. Effects of a Low-Element Challenge Course on Abstinence Self-Efficacy and Group Cohesion

    ERIC Educational Resources Information Center

    Clem, Jamie M.; Smith, Thomas E.; Richards, Kristin V.

    2012-01-01

    Substance abuse researchers identify self-efficacy and group cohesion as important components in alcohol and other drug-dependency treatment. Objectives: The purpose of this single-group, pretest-posttest study is to explore the therapeutic value of a challenge course intervention on the self-efficacy and group cohesion of nine chemically…

  7. Platinum group elements and 187Os/ 188Os in a purported impact ejecta layer near the Eifelian-Givetian stage boundary, Middle Devonian

    NASA Astrophysics Data System (ADS)

    Schmitz, Birger; Ellwood, Brooks B.; Peucker-Ehrenbrink, Bernhard; El Hassani, Ahmed; Bultynck, Pierre

    2006-09-01

    A global faunal crisis close to the Eifelian-Givetian stage boundary in the mid-Devonian has been purported to be related to the impact of one or two major extraterrestrial bodies. This was based on unusual mineralogical and chemical features within a distinct composite marl bed, at a level c. 40 cm below the Global Stratotype Section and Point (GSSP) for the Eifelian-Givetian boundary at Jebel Mech Irdane in Morocco. The impact relation has been challenged based partly on the absence of platinum group element data. We present here detailed Ir, Os, Pd and Pt as well as Os isotopic data across the bed at Mech Irdane and from a correlated 10 cm bed at a nearby site, Rich Haroun. Iridium concentrations of 0.13-0.28 ng/g in the beds represent a small enrichment compared to average shale, but Ir/Al ratios are only a factor 1.5-2 higher than background at respective site. Such small enrichments can readily be explained by terrestrial diagenetic processes, and do not require the presence of an extraterrestrial component. On an Al-normalized basis Pd and Pt show weak enrichments, typically a factor 2-4 higher than background. High 187Os/ 188Os ratios, 1.1-3.8, reflect ingrowth of radiogenic Os from Re, which is also evident from Os concentrations of up to 3 ng/g. The platinum group inter-element ratios are clearly non-chondritic. The overall platinum group and trace element (e.g. Co, Ni, As, V) patterns indicate that diagenetic processes at redox fronts have played a crucial role in shaping most element enrichments. If an excess siderophile-rich extraterrestrial component exists in these beds it represents less than 0.2‰ by weight.

  8. 75 FR 29531 - Resale Power Group of Iowa, WPPI Energy v. ITC Midwest LLC, Interstate Power and Light Company...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-05-26

    .... EL10-68-000] Resale Power Group of Iowa, WPPI Energy v. ITC Midwest LLC, Interstate Power and Light... Energy (Complainants) filed a formal complaint against ITC Midwest LLC and Interstate Power and...

  9. Platinum-Group Element Mineralization in the Fedorovatundra layered intrusion, Kola Peninsula, Russia

    NASA Astrophysics Data System (ADS)

    Groshev, Nikolay; Subbotin, Victor; Korchagin, Alexey

    2016-04-01

    The 2526 to 2485 Ma Fedorovatundra layered mafic intrusion in the central part of the Kola Peninsula, Russia, is the western massif of the Fedorova-Pana Complex (2526-2446 Ma), which is situated along the northern contact of the Early Proterozoic Imandra-Varzuga rift and Archean granite gneiss. The Fedorovatundra intrusion of approximately 4 km thick has two major parts: (1) located at the bottom of the intrusion Taxitic series (10 to 900 m) and composing the main volume of the massif Layered series (4000 m). The Taxitic series is distinctive, due to its predominant vary-textured often quartz-saturated norites and gabbronorites (with fewer amounts of leucogabbro, melanorite and Ol-gabbronorite) and abundant pyroxenite, less harzburgite xenoliths. Medium to coarse-grained mottled or massive leucocratic gabbronorite and leucogabbro prevails in the Layered series with mesocratic gabbronorite, pyroxenite and troctolite as subordinate rocks. Depending on its localization, geochemical features, mineral composition and economic value platinum-group element (PGE) mineralization of the Fedorovatundra intrusion is divided into 'marginal' (basal, contact) and 'reef' types. 'Marginal' type of mineralization is presented by irregular disseminated interstitial sulfides (1-2 vol. %) of pentlandite-pyrrhotite-chalcopyrite association (Cu/Ni = 1.8) in the Taxitic series. Less sulfides occur as uniformly disseminated aggregates, thin massive lenses and nests. PGE and base metals are concentrated in several ore horizons of 3.5 km long complicated structure. Thickness of ore horizons varies generally within 10-150 m, but it can rise up to 280 m in bulges. In the most common ore-bearing rock (taxitic gabbronorite) average Pt + Pd content is 1.6 ppm (Pd/Pt 4.5). The pyroxenite xenoliths occurring within the Taxitic series are practically barren of sulfide and can dilute higher PGE and base metal grades in the gabbronorite matrix. 'Marginal' mineralization of the Fedorovotundrovsky

  10. Measurements of Ultra-Heavy Elements in Solar Energetic Particle Events Above 10 MeV/nucleon

    NASA Astrophysics Data System (ADS)

    Leske, R. A.; Cohen, C. M.; Cummings, A. C.; Mewaldt, R. A.; Stone, E. C.; Wiedenbeck, M. E.; von Rosenvinge, T. T.

    2005-12-01

    Recent measurements from Wind/LEMT and ACE/ULEIS show that abundances of elements heavier than Ni (Z=28) can be enhanced relative to oxygen by factors of ~100 to 1000 (depending on species) in impulsive solar energetic particle (SEP) events at energies below several MeV/nucleon. The Solar Isotope Spectrometer (SIS) on ACE measures the composition of energetic nuclei for elements up to ~Zr (Z=40) at energies from ~10 to >100 MeV/nucleon. At these energies, even large gradual events often are very iron rich and may appear similar in composition to impulsive events, perhaps due to admixtures of flare seed material. Since August 1997, SIS has recorded ~1000 nuclei with Z≥29, including measurable quantities of Zn, Ge and Se (Z=30, 32, and 34). We present observations that establish the potential of extending ultra-heavy SEP measurements up to higher energies in order to test models of acceleration and abundance enhancements in both gradual and impulsive events. We find that the long-term average composition for elements from Z=30 to 40 appears to be similar to standard solar system values above 10 MeV/nucleon, but that there is considerable event-to-event variability. In particular, the event of 23 July 2004 is found to have very large enhancements in ultra-heavy ions at energies >10 MeV/nucleon, with a (34

  11. Survey of chimeric IStron elements in bacterial genomes: multiple molecular symbioses between group I intron ribozymes and DNA transposons

    PubMed Central

    Tourasse, Nicolas J.; Stabell, Fredrik B.; Kolstø, Anne-Brit

    2014-01-01

    IStrons are chimeric genetic elements composed of a group I intron associated with an insertion sequence (IS). The group I intron is a catalytic RNA providing the IStron with self-splicing ability, which renders IStron insertions harmless to the host genome. The IS element is a DNA transposon conferring mobility, and thus allowing the IStron to spread in genomes. IStrons are therefore a striking example of a molecular symbiosis between unrelated genetic elements endowed with different functions. In this study, we have conducted the first comprehensive survey of IStrons in sequenced genomes that provides insights into the distribution, diversity, origin and evolution of IStrons. We show that IStrons have a restricted phylogenetic distribution limited to two bacterial phyla, the Firmicutes and the Fusobacteria. Nevertheless, diverse IStrons representing two major groups targeting different insertion site motifs were identified. This taken with the finding that while the intron components of all IStrons belong to the same structural class, they are fused to different IS families, indicates that multiple intron–IS symbioses have occurred during evolution. In addition, introns and IS elements related to those that were at the origin of IStrons were also identified. PMID:25324310

  12. Potential-model calculation of an order-v2 nonrelativistic QCD matrix element

    NASA Astrophysics Data System (ADS)

    Bodwin, Geoffrey T.; Kang, Daekyoung; Lee, Jungil

    2006-07-01

    We present two methods for computing dimensionally regulated nonrelativistic QCD heavy-quarkonium matrix elements that are related to the second derivative of the heavy-quarkonium wave function at the origin. The first method makes use of a hard-cutoff regulator as an intermediate step and requires knowledge only of the heavy-quarkonium wave function. It involves a significant cancellation that is an obstacle to achieving high numerical accuracy. The second method is more direct and yields a result that is identical to the Gremm-Kapustin relation, but it is limited to use in potential models. It can be generalized to the computation of matrix elements of higher order in the heavy-quark velocity and can be used to resum the contributions to decay and production rates that are associated with those matrix elements. We apply these methods to the Cornell potential model and compute a matrix element for the J/ψ state that appears in the leading relativistic correction to the production and decay of that state through the color-singlet quark-antiquark channel.

  13. Platinum group elements in a 3.5 Ga nickel-iron occurrence - Possible evidence of a deep mantle origin

    NASA Technical Reports Server (NTRS)

    Tredoux, Marian; Hart, Rodger J.; Lindsay, Nicholas M.; De Wit, Maarten J.; Armstrong, Richard A.

    1989-01-01

    This paper reports the results of new field observations and the geochemical analyses for the area of the Bon Accord (BA) (the Kaapvaal craton, South Africa) Ni-Fe deposit, with particular consideration given to the trace element, platinum-group element, and isotopic (Pb, Nd, and Os) compositions. On the basis of these data, an interpretation of BA is suggested, according to which the BA deposit is a siderophile-rich heterogeneity remaining in the deep mantle after a process of incomplete core formation. The implications of such a model for the study of core-mantle segregation and the geochemistry of the lowermost mantle are discussed.

  14. Report of the IAU Working Group on Cartographic Coordinates and Rotational Elements of the Planets and Satellites

    USGS Publications Warehouse

    Davies, M.E.; Abalakin, V.K.; Cross, C.A.; Duncombe, R.L.; Masursky, H.; Morando, B.; Owen, T.C.; Seidelmann, P.K.; Sinclair, A.T.; Wilkins, G.A.; Tjuflin, Y.S.

    1980-01-01

    This paper is the entire report of the IAU Working Group on Cartographic Coordinates and Rotational Elements of the Planets and Satellites, including three annexes. Tables give the recemmended values for the directions of the north poles of rotation and the prime meridians of the planets and satellites. Reference surfaces for mapping these bodies are described. The annexes discuss the guiding principles, given in the body of the report, present explanatory notes, and provide a bibliography of the rotational elements and reference surfaces of the planets and satellites, definitions, and algebraic expressions of relevant parameters. ?? 1980 D. Reidel Publishing Co.

  15. Compressive Strength Evaluation in Brazed ZrO2/Ti6Al4V Joints Using Finite Element Analysis

    NASA Astrophysics Data System (ADS)

    Sharma, Ashutosh; Kee, Se Ho; Jung, Flora; Heo, Yongku; Jung, Jae Pil

    2016-05-01

    This study aims to synthesize and evaluate the compressive strength of the ZrO2/Ti-6Al-4V joint brazed using an active metal filler Ag-Cu-Sn-Ti, and its application to dental implants assuring its reliability to resist the compressive failure in the actual oral environment. The brazing was performed at a temperature of 750 °C for 30 min in a vacuum furnace under 5 × 10-6 Torr atmosphere. The microstructure of the brazed joint showed the presence of an Ag-rich matrix and a Cu-rich phase, and Cu-Ti intermetallic compounds were observed along the Ti-6Al-4V bonded interface. The compressive strength of the brazed ZrO2/Ti-6Al-4V joint was measured by EN ISO 14801 standard test method. The measured compressive strength of the joint was ~1477 MPa—a value almost five times that of existing dental cements. Finite element analysis also confirmed the high von Mises stress values. The compressive strains in the samples were found concentrated near the Ti-6Al-4V position, matching with the position of the real fractured sample. These results suggest extremely significant compressive strength in ZrO2/Ti-6Al-4V joints using the Ag-Cu-Sn-Ti filler. It is believed that a highly reliable dental implant can be processed and designed using the results of this study.

  16. Refractory inclusions from the Leoville, Efremovka, and Vigarano C3V chondrites - Major element differences between Types A and B, and extraordinary refractory siderophile element compositions

    NASA Technical Reports Server (NTRS)

    Sylvester, Paul J.; Simon, Steven B.; Grossman, Lawrence

    1993-01-01

    Instrumental neutron activation analysis is used to measure the bulk chemical compositions of ten Ca-, Al-rich inclusions (CAIs) from three C3V chondrites of the reduced subgroup, five from Leoville, three from Efremovka, and two from Vigarano. Six of the inclusions are found to possess very large fractionations between refractory siderophile elements, and four of the six have remarkably high concentrations of these siderophiles, as compared with CAIs analyzed previously. Most of the inclusions analyzed here have lower concentrations of Na, Au, Fe, Zn, and Mn than their Allende counterparts, consistent with the idea that they have experienced secondary alteration at a higher temperature or for a shorter time than did Allende inclusions.

  17. Multigram group separation of actinide and lanthanide elements by LiCl-based anion exchange

    SciTech Connect

    Collins, E.D.; Benker, D.E.; Chattin, F.R.; Orr, P.B.; Ross, R.G.

    1980-01-01

    The laboratory-scale LiCl AIX process has been successfully adapted to the multigram scale and has been used effectively in transuranium element production campaigns to separate the lanthanide fission products from the transplutonium actinides and to partition americium and curium from the heavier elements. Corrosion of the tantalum and glass equipment has been negligible. Although radiolytic gas generation has not caused a problem, radiation exposure of the Dowex 1-X10 anion exchange resin does occur significantly. However, the 1.3-L resin bed can be used successfully to process up to 3 batches, each containing 19 g of /sup 244/Cm (54 W of decay heat). The chromatographic elution process is controlled by use of an alpha detector in the column effluent line and by periodic measurement of the neutron profile of the column. The development and use of feed pretreatment and operating methods has enabled effective and dependable operation.

  18. Combined distillation and normal freezing to purify elements of groups II and VI

    NASA Technical Reports Server (NTRS)

    Holland, L. R.

    1984-01-01

    A practical system and its application to the purification of Te and Cd is described. Single crystals are grown directly in vitreous silica ampoules subsequently used for sealed Bridgman growth of (Hg-Cd)Te. The system also prepares the ampoules by heating in high vacuum. Purification of the elements is by the combined effect of distillation and normal freezing. Transport and segregation are discussed.

  19. Model of Silicon Refining During Tapping: Removal of Ca, Al, and Other Selected Element Groups

    NASA Astrophysics Data System (ADS)

    Olsen, Jan Erik; Kero, Ida T.; Engh, Thorvald A.; Tranell, Gabriella

    2016-12-01

    A mathematical model for industrial refining of silicon alloys has been developed for the so-called oxidative ladle refining process. It is a lumped (zero-dimensional) model, based on the mass balances of metal, slag, and gas in the ladle, developed to operate with relatively short computational times for the sake of industrial relevance. The model accounts for a semi-continuous process which includes both the tapping and post-tapping refining stages. It predicts the concentrations of Ca, Al, and trace elements, most notably the alkaline metals, alkaline earth metal, and rare earth metals. The predictive power of the model depends on the quality of the model coefficients, the kinetic coefficient, τ, and the equilibrium partition coefficient, L for a given element. A sensitivity analysis indicates that the model results are most sensitive to L. The model has been compared to industrial measurement data and found to be able to qualitatively, and to some extent quantitatively, predict the data. The model is very well suited for alkaline and alkaline earth metals which respond relatively fast to the refining process. The model is less well suited for elements such as the lanthanides and Al, which are refined more slowly. A major challenge for the prediction of the behavior of the rare earth metals is that reliable thermodynamic data for true equilibrium conditions relevant to the industrial process is not typically available in literature.

  20. Model of Silicon Refining During Tapping: Removal of Ca, Al, and Other Selected Element Groups

    NASA Astrophysics Data System (ADS)

    Olsen, Jan Erik; Kero, Ida T.; Engh, Thorvald A.; Tranell, Gabriella

    2017-04-01

    A mathematical model for industrial refining of silicon alloys has been developed for the so-called oxidative ladle refining process. It is a lumped (zero-dimensional) model, based on the mass balances of metal, slag, and gas in the ladle, developed to operate with relatively short computational times for the sake of industrial relevance. The model accounts for a semi-continuous process which includes both the tapping and post-tapping refining stages. It predicts the concentrations of Ca, Al, and trace elements, most notably the alkaline metals, alkaline earth metal, and rare earth metals. The predictive power of the model depends on the quality of the model coefficients, the kinetic coefficient, τ, and the equilibrium partition coefficient, L for a given element. A sensitivity analysis indicates that the model results are most sensitive to L. The model has been compared to industrial measurement data and found to be able to qualitatively, and to some extent quantitatively, predict the data. The model is very well suited for alkaline and alkaline earth metals which respond relatively fast to the refining process. The model is less well suited for elements such as the lanthanides and Al, which are refined more slowly. A major challenge for the prediction of the behavior of the rare earth metals is that reliable thermodynamic data for true equilibrium conditions relevant to the industrial process is not typically available in literature.

  1. Stabilization and highly metallic properties of heavy group-V hydrides at high pressures

    NASA Astrophysics Data System (ADS)

    Abe, Kazutaka; Ashcroft, N. W.

    2015-12-01

    Compressed hydrides of the heavy group-15 elements Bi and Sb are investigated using ab initio methods. While the hydrides of Bi and Sb are known to be quite unstable at one atmosphere, our calculations predict that they can be stabilized at high pressures. Thus, at the composition of XH 3 (X =Bi or Sb), possible Bi hydrides are BiH2(P n m a ) + H beyond 105 GPa and BiH3(I 41/a m d ) beyond 250 GPa; for Sb hydrides, SbH2 + H hardly appears, and SbH3(P n m a ) is stabilized beyond 150 GPa. All of these hydrides are metallic with very dispersive electronic structures, this being in accordance with the predictions of the Goldhammer-Herzfeld criterion. Superconducting transition temperatures have also been estimated from the extended McMillan equation, and they turn out to be 39 K for BiH2 at 125 GPa, 65 K for BiH3 at 270 GPa, and 68 K for SbH3 at 170 GPa.

  2. Method of loading organic materials with group III plus lanthanide and actinide elements

    DOEpatents

    Bell, Zane W.; Huei-Ho, Chuen; Brown, Gilbert M.; Hurlbut, Charles

    2003-04-08

    Disclosed is a composition of matter comprising a tributyl phosphate complex of a group 3, lanthanide, actinide, or group 13 salt in an organic carrier and a method of making the complex. These materials are suitable for use in solid or liquid organic scintillators, as in x-ray absorption standards, x-ray fluorescence standards, and neutron detector calibration standards.

  3. Threat to Valued Elements of Life: The Experience of Dementia across Three Ethnic Groups

    ERIC Educational Resources Information Center

    Lawrence, Vanessa; Samsi, Kritika; Banerjee, Sube; Morgan, Craig; Murray, Joanna

    2011-01-01

    Purpose: There is a fundamental knowledge gap regarding the experience of dementia within minority ethnic groups in the United Kingdom and elsewhere. The present study examined the subjective reality of living with dementia from the perspective of people with dementia within the 3 largest ethnic groups in the United Kingdom. Design and Methods:…

  4. Final Report: Main Group Element Chemistry in Service of Hydrogen Storage and Activation

    SciTech Connect

    David A. Dixon; Anthony J. Arduengo, III

    2010-09-30

    goal was met in terms of reducing the number of costly experiments and helping to focus the experimental effort on the potentially optimal targets. We have used computational chemistry approaches to predict the thermodynamic properties of a wide range of compounds containing boron, nitrogen, hydrogen, and other elements as appropriate including carbon. These calculations were done in most cases with high level molecular orbital theory methods that have small error bars on the order of ± 1 to 2 kcal/mol. The results were used to benchmark more approximate methods such as density functional theory for larger systems and for database development. We predicted reliable thermodynamics for thousands of compounds for release and regeneration schemes to aid/guide materials design and process design and simulation. These are the first reliable computed values for these compounds and for many represent the only available values. Overall, the computational results have provided us with new insights into the chemistry of main group and organic-base chemical hydrogen systems from the release of hydrogen to the regeneration of spent fuel. A number of experimental accomplishments were also made in this project. The experimental work on hydrogen storage materials centered on activated polarized σ- or π-bonded frameworks that hold the potential for ready dihydrogen activation, uptake, and eventually release. To this end, a large number of non-traditional valence systems including carbenes, cyanocarbons, and C-B and and B-N systems were synthesized and examined. During the course of these studies an important lead arose from the novel valency of a class of stable organic singlet bi-radical systems. A synthetic strategy to an “endless” hydrogen storage polymer has been developed based on our cyanocarbon chemistry. A key issue with the synthetic efforts was being able to link the kinetics of release with the size of the substituents as it was difficult to develop a low molecular

  5. Low keV electron probe analysis of silicate minerals for Mg, Al, and Si using pure-element standards

    NASA Technical Reports Server (NTRS)

    Cunningham, G. G.

    1972-01-01

    Accurate electron probe values for Mg, Al, and Si in silicate minerals may be obtained with pure-element standards. Analysis must be done at low (6 kV) accelerating potential and for best results, the average atomic number of the sample should be within about plus or minus 1 of the atomic number of the pure-element standard. This last requirement is automatically fulfilled for most common silicate minerals, as their average atomic numbers usually fall within the 11 to 15 range. Examples studied include a wet-chemically analyzed cordierite containing 17.71 weight percent Al, for which a value of 17.6 plus or minus 0.3 percent was obtained with the electron probe, and a hornblende containing 19.15 percent Si, which gave 19.0 plus or minus 0.3 percent using the probe method.

  6. 76 FR 7836 - PJM Power Providers Group v. PJM Interconnection, L.L.C.; Notice of Complaint

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-02-11

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF ENERGY Federal Energy Regulatory Commission PJM Power Providers Group v. PJM Interconnection, L.L.C.; Notice of... 385.206, PJM Power Providers Group (Complainant) filed a formal complaint against PJM...

  7. 75 FR 35786 - Resale Power Group of Iowa, WPPI Energy v. ITC Midwest LLC, Interstate Power and Light Company...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-06-23

    ... Group of Iowa and WPPI Energy filed a supplement to its complaint originally filed on May 18, 2010. Any... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF ENERGY Federal Energy Regulatory Commission Resale Power Group of Iowa, WPPI Energy v. ITC Midwest LLC, Interstate...

  8. Laser field induced optical gain in a group III-V quantum wire

    NASA Astrophysics Data System (ADS)

    Saravanan, Subramanian; Peter, Amalorpavam John; Lee, Chang Woo

    2016-08-01

    Effect of intense high frequency laser field on the electronic and optical properties of heavy hole exciton in an InAsP/InP quantum well wire is investigated taking into consideration of the spatial confinement. Laser field induced exciton binding energies, optical band gap, oscillator strength and the optical gain in the InAs0.8P0.2/InP quantum well wire are studied. The variational formulism is applied to find the respective energies. The laser field induced optical properties are studied. The optical gain as a function of photon energy, in the InAs0.8P0.2/InP quantum wire, is obtained in the presence of intense laser field. The compact density matrix method is employed to obtain the optical gain. The results show that the 1.55 μm wavelength for the fibre optic telecommunication applications is achieved for 45 Å wire radius in the absence of laser field intensity whereas the 1.55 μm wavelength is obtained for 40 Å if the amplitude of the laser field amplitude parameter is 50 Å. The characterizing wavelength for telecommunication network is optimized when the intense laser field is applied for the system. It is hoped that the obtained optical gain in the group III-V narrow quantum wire can be applied for fabricating laser sources for achieving the preferred telecommunication wavelength.

  9. FBG_SiMul V1.0: Fibre Bragg grating signal simulation tool for finite element method models

    NASA Astrophysics Data System (ADS)

    Pereira, G.; McGugan, M.; Mikkelsen, L. P.

    FBG_SiMul V1.0 is a tool to study and design the implementation of fibre Bragg grating (FBG) sensors solutions in any arbitrary loaded structure or application. The software removes the need for a fibre optic expert user and makes the sensor response of a structural health monitoring solution using FBG sensors more simple and fast. The software uses a modified T-Matrix method to simulate the FBG reflected spectrum based on the stress and strain from a finite element method model. The article describes the theory and algorithm implementation, followed by an empirical validation.

  10. The effect of interfacial failure around a class V composite restoration analysed by the finite element method.

    PubMed

    Rees, J S; Jacobsen, P H

    2000-02-01

    Partial failure around the tooth-composite interface of a class V restoration is common due to the effects of polymerization shrinkage. The effect that this has on the force distribution of the remaining intact interfaces has not been investigated. The aim of this study was to quantify the effect that partial failure of an isolated cavity wall interface had on the force distribution around the remaining intact interfaces of a class V composite restoration in a lower first premolar using a two-dimensional plane strain finite element model. Partial failure resulted in a 4-6-fold increase in peak tensile and shear forces compared to a tooth with a fully intact cavity wall interface. In some instances, the peak stresses were greater than the known bond strengths of composite to dentine.

  11. An Instrument to Measure Elemental Energy Spectra of Cosmic Ray Nuclei Up to 10(exp 16) eV

    NASA Technical Reports Server (NTRS)

    Adams, J.; Bashindzhagyan, G.; Chilingarian, A.; Drury, L.; Egorov, N.; Golubkov,S.; Korotkova, N.; Panasyuk, M.; Podorozhnyi, D.; Procqureur, J.

    2000-01-01

    A longstanding goal of cosmic ray research is to measure the elemental energy spectra of cosmic rays up to and through the "knee" (approx. equal to 3 x 10 (exp 15) eV. It is not currently feasible to achieve this goal with an ionization calorimeter because the mass required to be deployed in Earth orbit is very large (at least 50 tonnes). An alternative method will be presented. This is based on measuring the primary particle energy by determining the angular distribution of secondaries produced in a target layer using silicon microstrip detector technology. The proposed technique can be used over a wide range of energies (10 (exp 11)- 10 (exp 16) eV) and gives an energy resolution of 60% or better. Based on this technique, a design for a new lightweight instrument with a large aperture (KLEM) will be described.

  12. Effect of Element Substitution at V site on Thermoelectric Properties of Aurivillius Phase Bi2VO5.5

    NASA Astrophysics Data System (ADS)

    Kohri, Hitoshi; Yagasaki, Takayoshi

    2016-10-01

    Thermoelectric oxides are suitable at the high temperature range because of chemical stability. Aurivillius compounds are bismuth layered oxides, and known as oxygen ion conductors. The Aurivillius compounds consist of Perovskite layers and Bi-O layers. It is expected that nano-layered structure shows high Seebeck coefficients due to the quantum confinement of carriers in Perovskite layers. It was reported that the Seebeck coefficient of hot pressed specimens for Aurivillius phase Bi2VO5.5 was a high value of -28.3 mVK-1 at 1010 K, and the electrical resistivity of one was also a high value of 0.033 Ωm at 1010 K. In this paper, the effect of element substitution at the V site on thermoelectric properties of Aurivillius phase Bi2VO5.5 was investigated. Bi2V1- x M x O5.5 (M = Cr, Mo, W x = 0, 0.05, 0.1, 0.2) were prepared by solid-state reaction. The electrical resistivity of Cr-substituted specimens were indicated at larger values than the ones for unsubstituted specimens over the measurement temperature range. The resistivity above 800 K was reduced by substitution of W or Mo. W as a substituted element was effective for reducing the thermal conductivity of Bi2VO5.5. The maximum value of the dimensionless figure of merit ZT was 0.05 at 799 K for Bi2V0.8Mo0.2O5.5 and at 902 K for Bi2V0.8W0.1O5.5. The maximum ZT of an unsubstituted sample was 0.02 at 993 K. From these results, it was found that tungsten or molybdenum substitution was effective to improve ZT for Aurivillius phase Bi2VO5.5.

  13. Optimization of parameters for semiempirical methods V: modification of NDDO approximations and application to 70 elements.

    PubMed

    Stewart, James J P

    2007-12-01

    Several modifications that have been made to the NDDO core-core interaction term and to the method of parameter optimization are described. These changes have resulted in a more complete parameter optimization, called PM6, which has, in turn, allowed 70 elements to be parameterized. The average unsigned error (AUE) between calculated and reference heats of formation for 4,492 species was 8.0 kcal mol(-1). For the subset of 1,373 compounds involving only the elements H, C, N, O, F, P, S, Cl, and Br, the PM6 AUE was 4.4 kcal mol(-1). The equivalent AUE for other methods were: RM1: 5.0, B3LYP 6-31G*: 5.2, PM5: 5.7, PM3: 6.3, HF 6-31G*: 7.4, and AM1: 10.0 kcal mol(-1). Several long-standing faults in AM1 and PM3 have been corrected and significant improvements have been made in the prediction of geometries.

  14. Optimization of parameters for semiempirical methods V: Modification of NDDO approximations and application to 70 elements

    PubMed Central

    2007-01-01

    Several modifications that have been made to the NDDO core-core interaction term and to the method of parameter optimization are described. These changes have resulted in a more complete parameter optimization, called PM6, which has, in turn, allowed 70 elements to be parameterized. The average unsigned error (AUE) between calculated and reference heats of formation for 4,492 species was 8.0 kcal mol−1. For the subset of 1,373 compounds involving only the elements H, C, N, O, F, P, S, Cl, and Br, the PM6 AUE was 4.4 kcal mol−1. The equivalent AUE for other methods were: RM1: 5.0, B3LYP 6–31G*: 5.2, PM5: 5.7, PM3: 6.3, HF 6–31G*: 7.4, and AM1: 10.0 kcal mol−1. Several long-standing faults in AM1 and PM3 have been corrected and significant improvements have been made in the prediction of geometries. Figure Calculated structure of the complex ion [Ta6Cl12]2+ (footnote): Reference value in parenthesis Electronic supplementary material The online version of this article (doi:10.1007/s00894-007-0233-4) contains supplementary material, which is available to authorized users. PMID:17828561

  15. Anti-bactericidal properties of stingray Dasyatis pastinaca groups V, IIA, and IB phospholipases A2: a comparative study.

    PubMed

    Bacha, Abir Ben

    2014-10-01

    Group IIA secreted phospholipase A2 (group IIA sPLA2) is known to display potent Gram-positive bactericidal activity in vitro and in vivo. We have analyzed the bactericidal activity of the full set of native stingray and dromedary groups V, IIA, and IB sPLA2s on several Gram-positive and Gram-negative strains. The rank order potency among both marine and mammal sPLA2s against Gram-positive bacteria is group IIA > V > IB, whereas Gram-negative bacteria exhibited a much higher resistance. There is a synergic action of the sPLA2 with lysozyme when added to the bacteria culture prior to sPLA2.The bactericidal efficiency of groups V and IIA sPLA2s was shown to be dependent upon the presence of calcium ions and to a less extent Mg(2+) ions and then a correlation could be made to its hydrolytic activity of membrane phospholipids. Importantly, we showed that stingray and dromedary groups V, IIA, and IB sPLA2s present no cytotoxicity after their incubation with MDA-MB-231cells. stingray groups V and IIA sPLA2s, like mammal ones, may be considered as future therapeutic agents against bacterial infections.

  16. More than 1000 ultraconserved elements provide evidence that turtles are the sister group of archosaurs

    PubMed Central

    Crawford, Nicholas G.; Faircloth, Brant C.; McCormack, John E.; Brumfield, Robb T.; Winker, Kevin; Glenn, Travis C.

    2012-01-01

    We present the first genomic-scale analysis addressing the phylogenetic position of turtles, using over 1000 loci from representatives of all major reptile lineages including tuatara. Previously, studies of morphological traits positioned turtles either at the base of the reptile tree or with lizards, snakes and tuatara (lepidosaurs), whereas molecular analyses typically allied turtles with crocodiles and birds (archosaurs). A recent analysis of shared microRNA families found that turtles are more closely related to lepidosaurs. To test this hypothesis with data from many single-copy nuclear loci dispersed throughout the genome, we used sequence capture, high-throughput sequencing and published genomes to obtain sequences from 1145 ultraconserved elements (UCEs) and their variable flanking DNA. The resulting phylogeny provides overwhelming support for the hypothesis that turtles evolved from a common ancestor of birds and crocodilians, rejecting the hypothesized relationship between turtles and lepidosaurs. PMID:22593086

  17. Hair from different ethnic groups vary in elemental composition and nitrogen and phosphorus mineralisation in soil.

    PubMed

    Malepfane, N M; Muchaonyerwa, P

    2017-02-01

    Disposal of hair wastes at landfills causes nitrate leaching to ground water, and use of the waste as fertiliser could be a viable option. This study was to determine elemental composition of major hair types in South Africa and their nitrogen (N) and phosphorus (P) release in soil. Wastes of African, White and Indian hair were obtained from local salons and analysed for carbon (C), N and sulphur (S) with the Leco CNS analyzer, and P, bases, aluminium (Al) and micronutrients, with the ICP. We also conducted an incubation study to determine changes in mineral N and P in soil. Hair wastes were added to soil at increasing rates based on N, incubated at 25 °C with destructive sampling after 0, 28, 56 and 84 days and pH, ammonium-N, nitrate-N and extractable P measured. All data were subjected to analysis of variance. Indian and White hair had higher N than African. White hair had higher C and lower potassium (K) than those of other types. The Fe levels in hair were in the order White > African > Indian, whilst those of Al were African > Indian > White. African hair had higher calcium (Ca), manganese (Mn), zinc (Zn) and cobalt (Co) than the other types. Ammonium-N and nitrate-N releases were in the order: Indian > African > White, especially at higher rates. Ammonium-N increased in the first 28 days and declined thereafter, when nitrate-N increased and pH decreased. The findings implied that hair types differ in elemental composition and nitrogen release in soil, with implications on pollution and soil fertility.

  18. Which Social Elements Are Visible in Virtual Groups? Addressing the Categorization of Social Expressions

    ERIC Educational Resources Information Center

    Perez-Mateo, M.; Guitert, M.

    2012-01-01

    Learning is a social process. That is why it is extremely important to understand how students interact socially in online courses and how it affects the learning process. However, social aspects, understood as those expressions or comments that go beyond strictly academic interaction, i.e. the need to carry out group work, are not clearly…

  19. Effects of chemical functional groups on elemental mercury adsorption on carbonaceous surfaces.

    PubMed

    Liu, Jing; Cheney, Marcos A; Wu, Fan; Li, Meng

    2011-02-15

    A systematic theoretical study using density functional theory is performed to provide molecular-level understanding of the effects of chemical functional groups on mercury adsorption on carbonaceous surfaces. The zigzag and armchair edges were used in modeling the carbonaceous surfaces to simulate different adsorption sites. The edge atoms on the upper side of the models are unsaturated to simulate active sites. All calculations (optimizations, energies, and frequencies) were made at B3PW91 density functional theory level, using RCEP60VDZ basis set for mercury and 6-31G(d) pople basis set for other atoms. The results indicate that the embedding of halogen atom can increase the activity of its neighboring site which in turn increases the adsorption capacity of the carbonaceous surface for Hg(0). The adsorption belongs to chemisorptions, which is in good agreement with the experimental results. For the effects of oxygen functional groups, lactone, carbonyl and semiquinone favor Hg(0) adsorption because they increase the neighboring site's activity for mercury adsorption. On the contrary, phenol and carboxyl functional groups show a physisorption of Hg(0), and reduce Hg capture. This result can explain the seemingly conflicting experimental results reported in the literature concerning the influence of oxygen functional groups on mercury adsorption on carbonaceous surface.

  20. Crystal Field Theory and the Angular Overlap Model Applied to Hydrides of Main Group Elements.

    ERIC Educational Resources Information Center

    Moore, E. A.

    1990-01-01

    Described is how crystal field theory and the angular overlap model can be applied to very simple molecules which can then be used to introduce such concepts as bonding orbitals, MO diagrams, and Walsh diagrams. The main-group compounds are used as examples and a switch to the transition metal complexes. (KR)

  1. The group separation of the rare-earth elements and yttrium from geologic materials by cation-exchange chromatography

    USGS Publications Warehouse

    Crock, J.G.; Lichte, F.E.; Wildeman, T.R.

    1984-01-01

    Demand is increasing for the determination of the rare-earth elements (REE) and yttrium in geologic materials. Due to their low natural abundance in many materials and the interferences that occur in many methods of determination, a separation procedure utilizing gradient strong-acid cation-exchange chromatography is often used to preconcentrate and isolate these elements from the host-rock matrix. Two separate gradient strong-acid cation-exchange procedures were characterized and the major elements as well as those elements thought to provide the greatest interference for the determination of the REE in geologic materials were tested for separation from the REE. Simultaneous inductively coupled argon plasma-atomic emission spectroscopy (ICAP-AES) measurements were used to construct the chromatograms for the elution studies, allowing the elution patterns of all the elements of interest to be determined in a single fraction of eluent. As a rock matrix, U.S. Geological Survey standard reference BCR-1 basalt was digested using both an acid decomposition procedure and a lithium metaborate fusion. Hydrochloric and nitric acids were tested as eluents and chromatograms were plotted using the ICAP-AES data; and we observed substantial differences in the elution patterns of the REE and as well as in the solution patterns of Ba, Ca, Fe and Sr. The nitric acid elution required substantially less eluent to elute the REE and Y as a group when compared to the hydrochloric acid elution, and provided a clearer separation of the REE from interfering and matrix elements. ?? 1984.

  2. Siderophile element systematics of IAB complex iron meteorites: New insights into the formation of an enigmatic group

    NASA Astrophysics Data System (ADS)

    Worsham, Emily A.; Bermingham, Katherine R.; Walker, Richard J.

    2016-09-01

    Siderophile trace element abundances and the 187Re-187Os isotopic systematics of the metal phases of 58 IAB complex iron meteorites were determined in order to investigate formation processes and how meteorites within chemical subgroups may be related. Close adherence of 187Re-187Os isotopic data of most IAB iron meteorites to a primordial isochron indicates that the siderophile elements of most members of the complex remained closed to elemental disturbance soon after formation. Minor, presumably late-stage open-system behavior, however, is observed in some members of the sLM, sLH, sHL, and sHH subgroups. The new siderophile element abundance data are consistent with the findings of prior studies suggesting that the IAB subgroups cannot be related to one another by any known crystallization process. Equilibrium crystallization, coupled with crystal segregation, solid-liquid mixing, and subsequent fractional crystallization can account for the siderophile element variations among meteorites within the IAB main group (MG). The data for the sLM subgroup are consistent with equilibrium crystallization, combined with crystal segregation and mixing. By contrast, the limited fractionation of siderophile elements within the sLL subgroup is consistent with metal extraction from a chondritic source with little subsequent processing. The limited data for the other subgroups were insufficient to draw robust conclusions about crystallization processes involved in their formation. Collectively, multiple formational processes are represented in the IAB complex, and modeling results suggest that fractional crystallization within the MG may have been a more significant process than has been previously recognized.

  3. Theoretical predictions of properties and gas-phase chromatography behaviour of bromides of group-5 elements Nb, Ta, and element 105, Db

    NASA Astrophysics Data System (ADS)

    Pershina, V.; Anton, J.

    2012-01-01

    Fully relativistic, four-component density functional theory electronic structure calculations were performed for MBr5, MOBr3, MBr6-, KMBr6, and MBr5Cl- of group-5 elements Nb, Ta, and element 105, Db, with the aim to predict adsorption behaviour of the bromides in gas-phase chromatography experiments. It was shown that in the atmosphere of HBr/BBr3, the pentabromides are rather stable, and their stability should increase in the row Nb < Db < Ta. Several mechanisms of adsorption were considered. In the case of adsorption by van der Waals forces, the sequence in volatility of the pentabromides should be Nb < Ta < Db, being in agreement with the sublimation enthalpies of the Nb and Ta pentabromides. In the case of adsorption by chemical forces (on a quartz surface modified with KBr/KCl), formation of the MBr5L- (L = Cl, Br) complex should occur, so that the volatility should change in an opposite way, i.e., Nb > Ta > Db. This sequence is in agreement with the one observed in the "one-atom-at-a-time" chromatography experiments. Some other scenarios, such as surface oxide formation were also considered but found to be irrelevant.

  4. The conserved lymphokine element-0 in the IL5 promoter binds to a high mobility group-1 protein.

    PubMed

    Marrugo, J; Marsh, D G; Ghosh, B

    1996-10-01

    The conserved lymphokine elements-0 (CLE0) in the IL5 promoter is essential for the expression of IL-5. Here, we report the cloning and expression of a cDNA encoding a novel CLE0-binding protein, CLEBP-1 from a mouse Th2 clone, D10.G4.1. Interestingly, it was found that the CLEBP1 cDNA sequence was almost identical to the sequences of known high mobility group-1 (HMG1) cDNAs. When expressed as a recombinant fusion protein in Escherichia coli, CLEBP-1 was shown to bind to the IL5-CLE0 element in electrophoretic mobility-shift assays (EMSA) and southwestern blot analysis. The CLEBP-1 fusion protein cross-reacts with and-HMG-1/2 in Western blot analysis. It also binds to the CLE0 elements of IL4, GMCSF and GCSF genes. CLEBP-1 and closely related HMG-1 and HMG-2 proteins may play key roles in facilitating the expression of the lymphokine genes that contain CLE0 elements.

  5. Chromosomal Homology and Molecular Organization of Muller's Elements D and E in the Drosophila Repleta Species Group

    PubMed Central

    Ranz, J. M.; Segarra, C.; Ruiz, A.

    1997-01-01

    Thirty-three DNA clones containing protein-coding genes have been used for in situ hybridization to the polytene chromosomes of two Drosophila repleta group species, D. repleta and D. buzzatii. Twenty-six clones gave positive results allowing the precise localization of 26 genes and the tentative identification of another nine. The results were fully consistent with the currently accepted chromosomal homologies and in no case was evidence for reciprocal translocations or pericentric inversions found. Most of the genes mapped to chromosomes 2 and 4 that are homologous, respectively, to chromosome arms 3R and 3L of D. melanogaster (Muller's elements E and D). The comparison of the molecular organization of these two elements between D. melanogaster and D. repleta (two species that belong to different subgenera and diverged some 62 million years ago) showed an extensive reorganization via paracentric inversions. Using a maximum likelihood procedure, we estimated that 130 paracentric inversions have become fixed in element E after the divergence of the two lineages. Therefore, the evolution rate for element E is approximately one inversion per million years. This value is comparable to previous estimates of the rate of evolution of chromosome X and yields an estimate of 4.5 inversions per million years for the whole Drosophila genome. PMID:9071584

  6. Chemo-Dynamical Evolution of r-process Elements in the Local Group Galaxies

    NASA Astrophysics Data System (ADS)

    Hirai, Yutaka; Ishimaru, Yuhri; Saitoh, Takayuki R.; Fujii, Michiko S.; Hidaka, Jun; Kajino, Toshitaka

    The astrophysical site(s) of r-process is not yet identified over half a century. Astronomical high dispersion observations have shown that extremely metal-poor (EMP) stars in the Milky Way (MW) halo have large star-to-star dispersions in the abundance of r-process elements. Binary neutron star mergers (NSMs) are one of the most promising sites of r-process. However, several studies suggested that it is difficult to reproduce the dispersions by NSMs due to their long merger times and low rates. In this study, we performed a series of N-body/smoothed particle hydrodynamic simulations of dwarf galaxies. We show that NSMs can explain the dispersions with long merger times (˜100 Myr). We find that the metallicity of our simulated galaxies does not correlate with time in their early phase due to slow chemical enrichment. This slow chemical enrichment produces [Eu/Fe] distribution which is consistent with the observation. Our results suggest that stars in the MW halo formed with a low star formation rate of less than 10 - 3M ȯ yr-1, which is common for typical dwarf galaxies in the MW. Our simulations support the scenario that early enrichment of the MW halo occurred in the framework of hierarchical structure formation.

  7. Finite element simulation of conventional and prestressed cutting of Ti6Al4V

    NASA Astrophysics Data System (ADS)

    Peng, Ruitao; Tang, Xinzi; Tan, Yuanqiang; Liu, Xiongwei

    2013-05-01

    Titanium alloys are known as difficult-to-machine materials, chip morphology plays a predominant role in determining machinability and tool wear during the machining of titanium alloys. Based on the finite element analysis and experimental validation, the cutting processes in conventional cutting and prestressed cutting of titanium alloy ring parts were explored respectively. The Johnson-Cook model expressed by equivalent plastic strain flow stress is utilized to describe the constitutive properties. A ductile fracture criterion based on the strain energy is applied to model the crack initiation and evolution during the chip segmentation. Cutting force as well as distributions of stress, temperature and equivalent plastic strain along cutting time were numerically compared. The results indicate that in conventional cutting and prestressed cutting, chips show the similar characteristic of continuous and regular serrated shape. Initial stress distribution of workpiece was changed by prestress, which correspondingly leads to the alteration of stress distribution in the subsurface layer. Prestress hardly influences the distributions of temperature and equivalent plastic strain on workpiece. The cutting force curves share the same average amplitude and analogous undulating rhythm.

  8. Trace element analysis of obsidian artifacts from a classic Maya residential group at Nohmul, Belize

    SciTech Connect

    Hammond, N.; Neivens, M.D.; Harbottle, G.

    1984-01-01

    Forty-nine obsidian artifacts from a classic period residential group at Nohmul, northern Belize, have been analyzed by neutron activation analysis. The majority of the samples originated from Ixtepeque, and the remainder from El Chayal. Increasing prominence of the Ixtepeque source from the late Classic into the Terminal Classic (i.e., before and after ca. A.D. 800) suggests greater use of a coastal distribution route known to have originated in the formative and to have remained in use through the colonial period.

  9. Crystallographic point groups of five-dimensional space. 1. Their elements and their subgroups.

    PubMed

    Veysseyre, R; Veysseyre, H

    2002-09-01

    The purpose of this work is to introduce a method with a view to obtaining the crystallographic point groups of five-dimensional space, i.e. the subgroups of the holohedries of these space crystal families. This paper is specifically devoted to numerical analysis, whereas the following ones deal with some applications to crystallography. These results have been obtained through a collaboration between two teams: H. Veysseyre (Institut Supérieur des Matériaux) for the numerical analysis, R. Veysseyre, D. Weigel and Th. Phan (Ecole Centrale Paris) for the crystallographic part.

  10. Effect of process parameters on deep drawing of Ti-6Al-4V alloy using finite element analysis

    NASA Astrophysics Data System (ADS)

    Kotkunde, Nitin; Deole, Aditya D.; Gupta, A. K.; Singh, S. K.

    2013-12-01

    Deep drawing process depends on the large number of process parameters and their interdependence. Optimization of process parameters in deep drawing is a vital task to reduce manufacturing cost and understand their influence on the deformation behaviour of the sheet metal. In this paper, significance of important process parameters namely, punch speed, blank holder pressure (BHP) and temperature on the deep-drawing characteristics of a Ti-6Al-4V alloy are investigated. Taguchi technique was employed to identify the influence of these parameters on thickness distribution. The finite element model of deep drawing process has been built up and analyzed using Dynaform version 5.6.1 with LS-Dyna version 971 as solver. Based on the predicted thickness distribution of the deep drawn circular cup and analysis of variance (ANOVA) results, it is concluded that punch speed has the greatest influence on the deep drawing of Ti-6Al-4V alloy blank sheet. Temperature and BHP effect are negligible in deep drawing of Ti-6Al-4V alloy at low warm temperatures (less than 450°C) but it may contribute to a significant extent at higher temperature. Also thickness distribution is predicted using artificial neural network (ANN). It is observed that the predicted thickness distribution is in good agreement with the experimental data.

  11. Compendation of SSC lattice optics in the presence of dipole field errors: Report of the Correction Element Working Group

    SciTech Connect

    Bintinger, D.; Chao, A.; Forest, E.

    1989-02-01

    The assignment of the Correction Element Working Group (CEWG) is to advance the designs of various candidate correction schemes to a point where they can be compared and distilled down to a single plan. Choosing among, the options often involves consideration of incommensurate factors such as cost, practicality, and theoretical performance. Except for minor issues, the CEWG purpose is to gather and array the facts in a form from which these decisions can be rationally made, but not to make the decisions. The present report analyses various schemes for compensating nonlinear multipole errors in the main arc dipoles of the Superconducting Super Collider. Emphasis is on comparing lumped and distributed compensation, on minimizing the total number of correction elements, and on reducing the sensitivity to closed-orbit errors.

  12. Enzymatic properties of stingray Dasyatis pastinaca group V, IIA and IB phospholipases A(2): a comparative study.

    PubMed

    Ben Bacha, Abir; Abid, Islem; Horchani, Habib; Mejdoub, Hafedh

    2013-11-01

    In the present study, we have purified the group V phospholipase from the heart of cartilaginous fish stingray Dasyatis pastinaca and compared its biochemical properties with group IIA (sPLA2-IIA) and IB (sPLA2-IB) phospholipases previously purified from pancreas and intestine, respectively. Group V phospholipase (sPLA2-V) was purified to homogeneity by heat treatment, ammonium sulphate precipitation and RP-HPLC. The N-terminal sequence of the purified sPLA2-V exhibits a high degree of homology with those of mammal. The enzyme was found to be monomeric with a molecular mass estimation of 14 kDa. The specific activity of the purified enzyme, measured at pH 8 and 37 °C was 52 U/mg. Like sPLA2-IB and sPLA2-IIA, the sPLA2-V is found to be stable between pH 3 and 11 after 30 min of incubation. The purified sPLA2-V retained 65% of its activity after 10 min of incubation at 70 °C and it absolutely requires Ca(2+) for enzymatic activity. In addition it displayed high tolerance to organic solvents. Kinetic parameters Kmapp, kcat and the deduced catalytic efficiency (kcat/Kmapp) of the purified group-V, -IB and -IIA PLA2s were determined using phosphatidylethanolamine (PE), phosphatidylcholine (PC) or phosphatidylserine (PS) as substrate. The three enzymes hydrolyze the zwiterionic PE and PC substrates more efficiently than anionic PS substrate.

  13. Synthesis and characterization of group V metal carbide and nitride catalysts

    NASA Astrophysics Data System (ADS)

    Kwon, Heock-Hoi

    1998-11-01

    Group V transition metal carbides and nitrides were prepared via the temperature programmed reaction (TPR) of corresponding oxides with NHsb3 or a CHsb4/Hsb2 mixture. Except for the tantalum compounds, phase-pure carbides and nitrides were prepared. The vanadium carbides and nitrides were the most active and selective catalysts. Therefore the principal focus of the research was the preparation, characterization, and evaluation of high surface area vanadium nitride catalysts. A series of vanadium nitrides with surface areas up to 60 msp2/g was prepared. Thermal gravimetric analysis coupled with x-ray diffraction and scanning electron microscopy indicated that the solid-state reaction proceeded by the sequential reduction of Vsb2Osb5 to VOsb{0.9} and concluded with the topotactic substitution of nitrogen for oxygen in VOsb{0.9}. The transformation of Vsb2Osb5 to VN was pseudomorphic. An experimental design was executed to determine effects of the heating rates and space velocities on the VN microstructures. The heating rates had minor effects on the surface areas and pore size distributions; however, increasing the space velocity significantly increased the surface area. The materials were mostly mesoporous. Oxygen chemisorption on the vanadium nitrides scaled linearly with the surface area. The corresponding O/Vsbsurface ratio was ≈0.6. The vanadium nitrides were active for butane activation and pyridine hydrodenitrogenation. During butane activation, their selectivities towards dehydrogenation products were as high as 98%. The major product in pyridine hydrodenitrogenation was pentane. The reaction rates increased almost linearly with the surface area suggesting that these reactions were structure insensitive. The vanadium nitrides were not active for crotonaldehyde hydrogenation; however, they catalyzed an interesting ring formation reaction that produced methylbenzaldehyde and xylene from crotonaldehyde. A new method was demonstrated for the production of very

  14. The coupling of thermochemistry and phase diagrams for group III-V semiconductor systems. Final report

    SciTech Connect

    Anderson, T.J.

    1998-07-21

    The project was directed at linking the thermochemical properties of III-V compound semiconductors systems with the reported phase diagrams. The solid-liquid phase equilibrium problem was formulated and three approaches to calculating the reduced standard state chemical potential were identified and values were calculated. In addition, thermochemical values for critical properties were measured using solid state electrochemical techniques. These values, along with the standard state chemical potentials and other available thermochemical and phase diagram data, were combined with a critical assessment of selected III-V systems. This work was culminated with a comprehensive assessment of all the III-V binary systems. A novel aspect of the experimental part of this project was the demonstration of the use of a liquid encapsulate to measure component activities by a solid state emf technique in liquid III-V systems that exhibit high vapor pressures at the measurement temperature.

  15. Average bond energies between boron and elements of the fourth, fifth, sixth, and seventh groups of the periodic table

    NASA Technical Reports Server (NTRS)

    Altshuller, Aubrey P

    1955-01-01

    The average bond energies D(gm)(B-Z) for boron-containing molecules have been calculated by the Pauling geometric-mean equation. These calculated bond energies are compared with the average bond energies D(exp)(B-Z) obtained from experimental data. The higher values of D(exp)(B-Z) in comparison with D(gm)(B-Z) when Z is an element in the fifth, sixth, or seventh periodic group may be attributed to resonance stabilization or double-bond character.

  16. Osmium-Isotope and Platinum-Group-Element Systematics of Impact-Melt Rocks, Chesapeake Bay Impact Structure, Virginia, USA

    NASA Technical Reports Server (NTRS)

    Lee, Seung Ryeol; Wright Horton, J., Jr.; Walker, Richard J.

    2005-01-01

    Osmium (Os) isotopes and platinum-group elements (PGEs) are useful for geochemically identifying a meteoritic component within impact structures, because meteorites are typically characterized by low (187)Os/(188)Os ratios and high PGE concentrations. In contrast, most types of crustal target rocks have high radiogenic Os and very low PGE concentrations. We have examined Os isotope and PGE systematics of impact-melt rocks and pre-impact target rocks from a 2004 test hole in the late Eocene Chesapeake Bay impact structure and from nearby coreholes. Our goal is to determine the proportion of the projectile component in the melt rock Additional information is included in the original extended abstract.

  17. Mobilization of the platinum group elements by low-temperature fluids: Implications for mineralization and the iridium controversy

    NASA Technical Reports Server (NTRS)

    Dowling, Kim; Keays, Reid R.; Wallace, Malcolm W.; Gostin, Victor A.

    1992-01-01

    Geochemical investigations on the widely dispersed Late Proterozoic Acraman impact ejecta horizon and its host marine shales in the Adelaide Geosyncline provide strong evidence for low-temperature mobilization of the platinum group elements (PGE), including Ir. The ejecta horizon was formed when the middle Proterozoic dacitic volcanics in the Gawler Ranges, central South Australia, were impacted by a very large (ca. 4 km) meteorite. The resulting structure, now represented by Lake Acraman, is Australia's largest meteorite impact structure. Debris from the impact was blasted for many hundreds of kilometers, some falling into the shallow sea of the Adelaide Geosyncline, some 300 km to the east of the impact site.

  18. [Mechanism of renal elimination of 2 elements of group IIIA of the periodic table : aluminum and indium].

    PubMed

    Galle, P

    1981-01-05

    Aluminium and indium, two elements of group IIIA of the periodic table, are concentrated by the kidney inside lysosomes of proximal tubule cell. In these lysosomes, aluminium and indium are precipitated as non-soluble phosphate salts and these precipitates are then expelled in the tubular lumen and eliminated with the urinary flow. These data have been visualized by analytical microscopy (ion microscopy and X ray microanalysis). Local acid phosphatases are assumed to permit the concentration of aluminium and indium salts inside the lysosomes.

  19. NEUTRONIC REACTOR FUEL ELEMENT

    DOEpatents

    Shackleford, M.H.

    1958-12-16

    A fuel element possessing good stability and heat conducting properties is described. The fuel element comprises an outer tube formed of material selected from the group consisting of stainhess steel, V, Ti. Mo. or Zr, a fuel tube concentrically fitting within the outer tube and containing an oxide of an isotope selected from the group consisting of U/sup 235/, U/sup 233/, and Pu/sup 239/, and a hollow, porous core concentrically fitting within the fuel tube and formed of an oxide of an element selected from the group consisting of Mg, Be, and Zr.

  20. Modeling Group IV elements with new transferable tight-binding models

    SciTech Connect

    Kwon, I.; Biswas, R.

    1993-10-01

    An outstanding problem in the computer-based microscopic description of Group IV materials, is the need for an accurate transferable model of the energetic and electronic properties of semiconductor structures. The three complementary approaches have been the ab-initio method including Car-Parinello simulations, the classical molecular dynamics method, and tight-binding molecular dynamics. While being very accurate, the ab-initio molecular dynamics has been performed on small systems ({approximately}100 atoms) for short time scales ({approximately}10 ps). On the other hand, classical potential models have had much success in describing melting of silicon, amorphous silicon structures, thin film growth and a variety of computationally intensive molecular dynamics simulations. However, the classical based models do not contain important electronic information which is essential in a variety of problems in electronic materials such as determining the gap states for structural defects. The accuracy of the classical models in configurations, far from the fitting database, may be uncertain. Our approach is to find transferable tight-binding models for silicon that are in between the ab-initio simulations and the classical models for molecular dynamics in level of sophistication.

  1. Open-framework clathrates of group IV elements: Synthesis, structure, and characterization

    NASA Astrophysics Data System (ADS)

    Ramachandran, Ganesh K.

    This study addresses the synthesis, the characterization by x-ray diffraction and nuclear magnetic resonance (NMR) spectroscopy, and the measurement of the electrical properties of members of a class of compounds known as silicon and germanium clathrates. A quantitative 29Si NMR study of Na8Si 46 along with Rietveld refinement of site occupancies demonstrates that the compound is the stoichiometric clathrate Na8Si46, rather than an intermetallic Zintl compound containing silicon vacancies. In line with the observations on Na8Si46, the homologous K8Si46 and Rb6Si46 alkali-silicon clathrates are also observed to be fully stoichiometric at the framework sites, i.e., devoid of framework vacancies. In contrast two vacancies are formed predominantly at one-third of the crystallographic 6c tetrahedral sites in the homologous alkali-germanium and alkali-tin systems. This result is understood generally in terms of weaker Tt-Tt (Tt = Si, Ge, Sn) bonding as one descends the periodic table. The synthesis and characterization of the Structure II silicon clathrate NaxSi136 (x = 4--23) by powder x-ray diffraction combined with Rietveld profile analysis is also reported. In NaxSi 136, systematic changes in x-ray diffraction intensities enable the Na content and site occupancy to be characterized. In the same structure, we observe a 0.5% increase in the unit cell edge upon progressing from Na 4Si136 to Na23Si136. A statistical mechanical model combined with experimental data for this phase reveals a preference for the removal of sodium from the smaller of the two available cages by 0.190 +/- 0.050 eV. The Structure II clathrate Na16Cs8Si136 was synthesized employing the silicides of sodium and cesium as intermediates. In the same compound, large 23Na and 29Si Knight shifts are observed in 29Si magic angle spinning (MAS) NMR experiments. Electrical conductivity measurements on cold pressed samples of the material also indicate metallic behavior, with a room temperature value of rho

  2. 76 FR 39870 - PJM Interconnection, LLC; PJM Power Providers Group v. PJM Interconnection, LLC; Notice of Date...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-07

    ... presents an opportunity to exercise buyer market power; (2) whether the Fixed Resource Requirement (FRR... FRR option that allow parties to self-supply while deterring buyer market power. Parties will have 21... Energy Regulatory Commission PJM Interconnection, LLC; PJM Power Providers Group v. PJM...

  3. Indentation Pileup Behavior of Ti-6Al-4V Alloy: Experiments and Nonlocal Crystal Plasticity Finite Element Simulations

    NASA Astrophysics Data System (ADS)

    Han, Fengbo; Tang, Bin; Yan, Xu; Peng, Yifei; Kou, Hongchao; Li, Jinshan; Deng, Ying; Feng, Yong

    2017-01-01

    This study reports on the indentation pileup behavior of Ti-6Al-4V alloy. Berkovich nanoindentation was performed on a specimen with equiaxed microstructure. The indented area was characterized by electron backscattered diffraction (EBSD) to obtain the indented grain orientations. Surface topographies of several indents were measured by atomic force microscopy (AFM). The pileup patterns on the indented surfaces show significant orientation dependence. Corresponding nonlocal crystal plasticity finite element (CPFE) simulations were carried out to predict the pileup patterns. Analysis of the cumulative shear strain distributions and evolutions for different slip systems around the indents found that the pileups are mainly caused by prismatic slip. The pileup patterns evolve with the loading and unloading process, and the change in pileup height due to the elastic recovery at unloading stage is significant. The density distributions of geometrically necessary dislocations (GNDs) around the indent were predicted. Simulation of nanoindentation on a tricrystal model was performed.

  4. Indentation Pileup Behavior of Ti-6Al-4V Alloy: Experiments and Nonlocal Crystal Plasticity Finite Element Simulations

    NASA Astrophysics Data System (ADS)

    Han, Fengbo; Tang, Bin; Yan, Xu; Peng, Yifei; Kou, Hongchao; Li, Jinshan; Deng, Ying; Feng, Yong

    2017-04-01

    This study reports on the indentation pileup behavior of Ti-6Al-4V alloy. Berkovich nanoindentation was performed on a specimen with equiaxed microstructure. The indented area was characterized by electron backscattered diffraction (EBSD) to obtain the indented grain orientations. Surface topographies of several indents were measured by atomic force microscopy (AFM). The pileup patterns on the indented surfaces show significant orientation dependence. Corresponding nonlocal crystal plasticity finite element (CPFE) simulations were carried out to predict the pileup patterns. Analysis of the cumulative shear strain distributions and evolutions for different slip systems around the indents found that the pileups are mainly caused by prismatic slip. The pileup patterns evolve with the loading and unloading process, and the change in pileup height due to the elastic recovery at unloading stage is significant. The density distributions of geometrically necessary dislocations (GNDs) around the indent were predicted. Simulation of nanoindentation on a tricrystal model was performed.

  5. Control of GaP nanowire morphology by group V flux in gas source molecular beam epitaxy

    NASA Astrophysics Data System (ADS)

    Kuyanov, P.; Boulanger, J.; LaPierre, R. R.

    2017-03-01

    GaP nanowires (NWs) were grown on a Si substrate by gas source molecular beam epitaxy using self-assisted growth. Selective-area growth was achieved using a patterned oxide mask. Periodic GaAsP marker layers were introduced during growth to study the growth progression using transmission electron microscopy. We demonstrate control of the NW morphology via the V/III flux ratio, the pattern pitch, and the oxide hole diameter. As the V/III flux ratio was increased from 1 to 6, the NWs showed a reduced top diameter and increased height. Reduced oxide hole diameter and increased V/III flux ratio caused the Ga droplet to be consumed partway through the growth for some NWs, leading to a switch from VLS group V limited growth to diffusion limited growth.

  6. Spontaneous Double Hydrometallation Induced by N→M Coordination in Organometallic Hydrides of Group 14 Elements.

    PubMed

    Novák, Miroslav; Dostál, Libor; Turek, Jan; Alonso, Mercedes; De Proft, Frank; Růžička, Aleš; Jambor, Roman

    2016-04-11

    Our attempts to synthesise N→M intramolecularly coordinated diorganometallic hydrides L2MH2 [M=Si (4), Ge (5), Sn (6)] containing the CH=N imine group (in which L is C,N-chelating ligand {2-[(2,6-iPr2C6H3)N=CH]C6 H4}(-)) yielded 1,1'-bis(2,6-diisopropylphenyl)-2,2'-spriobi[benzo[c][1,2]azasilole] (7), 1,1'-bis(2,6-diisopropylphenyl)-2,2'-spriobi[benzo[c][1,2]azagermole] (8) and C,N-chelated homoleptic stannylene L2Sn (10), respectively. Compounds 7 and 8 are an outcome of a spontaneous double hydrometallation of the two CH=N imine moieties induced by N→M intramolecular coordination (M=Si, Ge) in the absence of any catalyst. In contrast, the diorganotin hydride L2SnH2 (6) is redox-unstable and the reduction of the tin centre with the elimination of H2 provided the C,N-chelated homoleptic stannylene L2Sn (10). Compounds 7 and 8 were characterised by NMR spectroscopy and X-ray diffraction analysis. Because the proposed N→M intramolecularly coordinated diorganometallic hydrides L2MH2 [M=Si (4), Ge (5), Sn (6)] revealed two different types of reduction reactions, DFT calculations were performed to gain an insight into the structures and bonding of the non-isolable diorganometallic hydrides as well as the products of their subsequent reactions. Furthermore, the thermodynamic profiles of the different reaction pathways with respect to the central metal atom were also investigated.

  7. Distribution of platinum-group elements in the Bati Kef chromite deposit, Guleman-Elazig area, eastern Turkey.

    USGS Publications Warehouse

    Page, N.J.; Engin, T.; Singer, D.A.; Haffty, J.

    1984-01-01

    The distribution of platinum-group elements (PGE) within chromite deposits from an ophiolite is determined and their geochemistry compared with chromitites from ophiolites and from stratiform layered complexes elsewhere in the world. The Guleman area chromitites are lenses of layered massive to disseminated chromite in dunite or sheared harzburgite along and near the dunite-harzburgite contact. PGE were analysed by a fire assay/spectrographic method. The analyses, in ppb, varied narrowly near the detection limits; only Ir was mostly detected (24-27 ppb) . The data plot as independent, slight variations of individual PGE with crude and irregular spatial distributions, oriented with respect to the land surface. Based on studies elsewhere, the PGE reside mostly in laurite, erlichmanite and Os/Ir alloys included within or interstitial to chromite. Average values for each PGE were normalized with respect to average chondrite concentrations for these elements. All patterns for ophiolite-chromitites (5) show depletion of these elements relative to chondrite average concentrations, with greater depletion in Pt and Pd than in Ir and Ru, to produce patterns with negative slopes. Chromitites from differentiated stratiform complexes (2) yield patterns with positive slopes. -G.J.N.

  8. BRAF-V600E expression in precursor versus differentiated dendritic cells defines clinically distinct LCH risk groups

    PubMed Central

    Berres, Marie-Luise; Lim, Karen Phaik Har; Peters, Tricia; Price, Jeremy; Takizawa, Hitoshi; Salmon, Hélène; Idoyaga, Juliana; Ruzo, Albert; Lupo, Philip J.; Hicks, M. John; Shih, Albert; Simko, Stephen J.; Abhyankar, Harshal; Chakraborty, Rikhia; Leboeuf, Marylene; Beltrão, Monique; Lira, Sérgio A.; Heym, Kenneth M.; Clausen, Björn E.; Bigley, Venetia; Collin, Matthew; Manz, Markus G.; McClain, Kenneth

    2014-01-01

    Langerhans cell histiocytosis (LCH) is a clonal disorder with elusive etiology, characterized by the accumulation of CD207+ dendritic cells (DCs) in inflammatory lesions. Recurrent BRAF-V600E mutations have been reported in LCH. In this study, lesions from 100 patients were genotyped, and 64% carried the BRAF-V600E mutation within infiltrating CD207+ DCs. BRAF-V600E expression in tissue DCs did not define specific clinical risk groups but was associated with increased risk of recurrence. Strikingly, we found that patients with active, high-risk LCH also carried BRAF-V600E in circulating CD11c+ and CD14+ fractions and in bone marrow (BM) CD34+ hematopoietic cell progenitors, whereas the mutation was restricted to lesional CD207+ DC in low-risk LCH patients. Importantly, BRAF-V600E expression in DCs was sufficient to drive LCH-like disease in mice. Consistent with our findings in humans, expression of BRAF-V600E in BM DC progenitors recapitulated many features of the human high-risk LCH, whereas BRAF-V600E expression in differentiated DCs more closely resembled low-risk LCH. We therefore propose classification of LCH as a myeloid neoplasia and hypothesize that high-risk LCH arises from somatic mutation of a hematopoietic progenitor, whereas low-risk disease arises from somatic mutation of tissue-restricted precursor DCs. PMID:24638167

  9. A Meiotic Drive Element in the Maize Pathogen Fusarium verticillioides Is Located Within a 102 kb Region of Chromosome V

    PubMed Central

    Pyle, Jay; Patel, Tejas; Merrill, Brianna; Nsokoshi, Chabu; McCall, Morgan; Proctor, Robert H.; Brown, Daren W.; Hammond, Thomas M.

    2016-01-01

    Fusarium verticillioides is an agriculturally important fungus because of its association with maize and its propensity to contaminate grain with toxic compounds. Some isolates of the fungus harbor a meiotic drive element known as Spore killer (SkK) that causes nearly all surviving meiotic progeny from an SkK × Spore killer-susceptible (SkS) cross to inherit the SkK allele. SkK has been mapped to chromosome V but the genetic element responsible for meiotic drive has yet to be identified. In this study, we used cleaved amplified polymorphic sequence markers to genotype individual progeny from an SkK × SkS mapping population. We also sequenced the genomes of three progeny from the mapping population to determine their single nucleotide polymorphisms. These techniques allowed us to refine the location of SkK to a contiguous 102 kb interval of chromosome V, herein referred to as the Sk region. Relative to SkS genotypes, SkK genotypes have one extra gene within this region for a total of 42 genes. The additional gene in SkK genotypes, herein named SKC1 for Spore Killer Candidate 1, is the most highly expressed gene from the Sk region during early stages of sexual development. The Sk region also has three hyper-variable regions, the longest of which includes SKC1. The possibility that SKC1, or another gene from the Sk region, is an essential component of meiotic drive and spore killing is discussed. PMID:27317777

  10. "Reference values" of trace elements in the hair of a sample group of Spanish children (aged 6-9 years) - are urban topsoils a source of contamination?

    PubMed

    Peña-Fernández, A; González-Muñoz, M J; Lobo-Bedmar, M C

    2014-07-01

    Human hair is used as a biomonitor to evaluate the environmental exposure to contaminants in the individual. However, the use of human hair is controversial, mainly because reference levels for pollutants in hair have not yet been set. In the case of Spain, few biomonitoring studies have involved infants and children. A biomonitoring study was conducted to investigate the possible normal values of trace elements of toxicological concern in children aged 6-9 years from the city of Alcalá de Henares, Community of Madrid (Spain), following the methodology and strict inclusion criteria previously developed by our group. Levels of Al, As, Be, Cd, Cr, Cu, Hg, Mn, Ni, Pb, Sn, Ti, Tl, V and Zn were monitored in scalp-hair from 117 healthy children (47 boys and 70 girls) between April and May of 2001. The levels of trace elements here described could be considered as possible "reference values" for children aged 6-9 years resident in the Community of Madrid. These values might also be selected as a preliminary screening tool to evaluate if a Spanish child has been exposed to any of the contaminants studied here. This study also investigated whether local urban topsoils were a source of metals for this population.

  11. Finite Element Simulations of Micro Turning of Ti-6Al-4V using PCD and Coated Carbide tools

    NASA Astrophysics Data System (ADS)

    Jagadesh, Thangavel; Samuel, G. L.

    2016-07-01

    The demand for manufacturing axi-symmetric Ti-6Al-4V implants is increasing in biomedical applications and it involves micro turning process. To understand the micro turning process, in this work, a 3D finite element model has been developed for predicting the tool chip interface temperature, cutting, thrust and axial forces. Strain gradient effect has been included in the Johnson-Cook material model to represent the flow stress of the work material. To verify the simulation results, experiments have been conducted at four different feed rates and at three different cutting speeds. Since titanium alloy has low Young's modulus, spring back effect is predominant for higher edge radius coated carbide tool which leads to the increase in the forces. Whereas, polycrystalline diamond (PCD) tool has smaller edge radius that leads to lesser forces and decrease in tool chip interface temperature due to high thermal conductivity. Tool chip interface temperature increases by increasing the cutting speed, however the increase is less for PCD tool as compared to the coated carbide tool. When uncut chip thickness decreases, there is an increase in specific cutting energy due to material strengthening effects. Surface roughness is higher for coated carbide tool due to ploughing effect when compared with PCD tool. The average prediction error of finite element model for cutting and thrust forces are 11.45 and 14.87 % respectively.

  12. Finite Element Simulations of Micro Turning of Ti-6Al-4V using PCD and Coated Carbide tools

    NASA Astrophysics Data System (ADS)

    Jagadesh, Thangavel; Samuel, G. L.

    2017-02-01

    The demand for manufacturing axi-symmetric Ti-6Al-4V implants is increasing in biomedical applications and it involves micro turning process. To understand the micro turning process, in this work, a 3D finite element model has been developed for predicting the tool chip interface temperature, cutting, thrust and axial forces. Strain gradient effect has been included in the Johnson-Cook material model to represent the flow stress of the work material. To verify the simulation results, experiments have been conducted at four different feed rates and at three different cutting speeds. Since titanium alloy has low Young's modulus, spring back effect is predominant for higher edge radius coated carbide tool which leads to the increase in the forces. Whereas, polycrystalline diamond (PCD) tool has smaller edge radius that leads to lesser forces and decrease in tool chip interface temperature due to high thermal conductivity. Tool chip interface temperature increases by increasing the cutting speed, however the increase is less for PCD tool as compared to the coated carbide tool. When uncut chip thickness decreases, there is an increase in specific cutting energy due to material strengthening effects. Surface roughness is higher for coated carbide tool due to ploughing effect when compared with PCD tool. The average prediction error of finite element model for cutting and thrust forces are 11.45 and 14.87 % respectively.

  13. Platinum group elements and gold in ferromanganese crusts from Afanasiy-Nikitin seamount, equatorial Indian Ocean: Sources and fractionation

    USGS Publications Warehouse

    Banakar, V.K.; Hein, J.R.; Rajani, R.P.; Chodankar, A.R.

    2007-01-01

    The major element relationships in ferromanganese (Fe-Mn) crusts from Afanasiy-Nikitin seamount (ANS), eastern equatorial Indian Ocean, appear to be atypical. High positive correlations (r = 0.99) between Mn/Co and Fe/Co ratios, and lack of correlation of those ratios with Co, Ce, and Ce/Co, indicate that the ANS Fe-Mn crusts are distinct from Pacific seamount Fe-Mn crusts, and reflect region-specific chemical characteristics. The platinum group elements (PGE: Ir, Ru, Rh, Pt, and Pd) and Au in ANS Fe-Mn crusts are derived from seawater and are mainly of terrestrial origin, with a minor cosmogenic component. The Ru/Rh (0.5-2) and Pt/Ru ratios (7-28) are closely comparable to ratios in continental basalts, whereas Pd/Ir ratios exhibit values ( 0.75) correlations between water depth and Mn/Co, Fe/Co, Ce/Co, Co, and the PGEs. Fractionation of the PGE-Au from seawater during colloidal precipitation of the major-oxide phases is indicated by well-defined linear positive correlations (r > 0.8) of Co and Ce with Ir, Ru, Rh, and Pt; Au/Co with Mn/Co; and by weak or no correlations of Pd with water depth, Co-normalized major-element ratios, and with the other PGE (r < 0.5). The strong enrichment of Pt (up to 1 ppm) relative to the other PGE and its positive correlations with Ce and Co demonstrate a common link for the high concentrations of all three elements, which likely involves an oxidation reaction on the Mn-oxide and Fe-oxyhydroxide surfaces. The documented fractionation of PGE-Au and their positive association with redox sensitive Co and Ce may have applications in reconstructing past-ocean redox conditions and water masses.

  14. Les Houches 2015: Physics at TeV Colliders Standard Model Working Group Report

    SciTech Connect

    Andersen, J.R.; et al.

    2016-05-16

    This Report summarizes the proceedings of the 2015 Les Houches workshop on Physics at TeV Colliders. Session 1 dealt with (I) new developments relevant for high precision Standard Model calculations, (II) the new PDF4LHC parton distributions, (III) issues in the theoretical description of the production of Standard Model Higgs bosons and how to relate experimental measurements, (IV) a host of phenomenological studies essential for comparing LHC data from Run I with theoretical predictions and projections for future measurements in Run II, and (V) new developments in Monte Carlo event generators.

  15. A redshift survey of IRAS galaxies. V - The acceleration on the Local Group

    NASA Technical Reports Server (NTRS)

    Strauss, Michael A.; Yahil, Amos; Davis, Marc; Huchra, John P.; Fisher, Karl

    1992-01-01

    The acceleration on the Local Group is calculated based on a full-sky redshift survey of 5288 galaxies detected by IRAS. A formalism is developed to compute the distribution function of the IRAS acceleration for a given power spectrum of initial perturbations. The computed acceleration on the Local Group points 18-28 deg from the direction of the Local Group peculiar velocity vector. The data suggest that the CMB dipole is indeed due to the motion of the Local Group, that this motion is gravitationally induced, and that the distribution of IRAS galaxies on large scales is related to that of dark matter by a simple linear biasing model.

  16. Identification of polycomb and trithorax group responsive elements in the regulatory region of the Drosophila homeotic gene Sex combs reduced

    SciTech Connect

    Gindhart, J.G. Jr.; Kaufman, T.C.

    1995-02-01

    The Drosophilia homeotic gene Sex combs reduced (Scr) is necessary for the establishment and maintenance of the morphological identity of the labial and prothoracic segments. In the early embryo, its expression pattern is established through the activity of several gap and segmentation gene products, as well as other transcription factors. Once established, the Polycomb group (Pc-G) and trithorax group (trx-G) gene products maintain the spatial pattern of Scr expression for the remainder of development. We report the identification of DNA fragments in the Scr regulatory region that may be important for its regulation by Polycomb and trithorax group gene products. When DNA fragments containing these regulatory sequences are subcloned into P-element vectors containing a white minigene, transformants containing these constructs exhibit mosaic patterns of pigmentation in the adult eye, indicating that white minigene expression is repressed in a clonally heritable manner. The size of pigmented and nonpigmented clones in the adult eye suggests that the event determining whether a cell in the eye anlagen will express white occurs at least as early as the first larval instar. The amount of white minigene repression is reduced in some Polycomb group mutants, whereas repression is enhanced in flies mutant for a subset of trithorax group loci. The repressor activity of one fragment, normally located in Scr Intron 2, is increased when it is able to homologously pair, a property consistent with genetic data suggesting that Scr exhibits transvection. Another Scr regulatory fragment, normally located 40 kb upstream of the Scr promoter, silences ectopic expression of an Scr-lacZ fusion gene in the embryo and does so in a Polycomb-dependent manner. We propose that the regulatory sequences located within these DNA fragments may normally mediate the regulation of Scr by proteins encoded by members of Polycomb and trithorax group loci. 98 refs., 6 figs., 4 tabs.

  17. Streptococcal group B integrative and mobilizable element IMESag-rpsI encodes a functional relaxase involved in its transfer

    PubMed Central

    Lorenzo-Diaz, Fabian; Fernández-Lopez, Cris; Douarre, Pierre-Emmanuel; Baez-Ortega, Adrian; Flores, Carlos; Glaser, Philippe

    2016-01-01

    Streptococcus agalactiae or Group B Streptococcus (GBS) are opportunistic bacteria that can cause lethal sepsis in children and immuno-compromised patients. Their genome is a reservoir of mobile genetic elements that can be horizontally transferred. Among them, integrative and conjugative elements (ICEs) and the smaller integrative and mobilizable elements (IMEs) primarily reside in the bacterial chromosome, yet have the ability to be transferred between cells by conjugation. ICEs and IMEs are therefore a source of genetic variability that participates in the spread of antibiotic resistance. Although IMEs seem to be the most prevalent class of elements transferable by conjugation, they are poorly known. Here, we have studied a GBS-IME, termed IMESag-rpsI, which is widely distributed in GBS despite not carrying any apparent virulence trait. Analyses of 240 whole genomes showed that IMESag-rpsI is present in approximately 47% of the genomes, has a roughly constant size (approx. 9 kb) and is always integrated at a single location, the 3′-end of the gene encoding the ribosomal protein S9 (rpsI). Based on their genetic variation, several IMESag-rpsI types were defined (A–J) and classified in clonal complexes (CCs). CC1 was the most populated by IMESag-rpsI (more than 95%), mostly of type-A (71%). One CC1 strain (S. agalactiae HRC) was deep-sequenced to understand the rationale underlying type-A IMESag-rpsI enrichment in GBS. Thirteen open reading frames were identified, one of them encoding a protein (MobSag) belonging to the broadly distributed family of relaxases MOBV1. Protein MobSag was purified and, by a newly developed method, shown to cleave DNA at a specific dinucleotide. The S. agalactiae HRC-IMESag-rpsI is able to excise from the chromosome, as shown by the presence of circular intermediates, and it harbours a fully functional mobilization module. Further, the mobSag gene encoded by this mobile element is able to promote plasmid transfer among pneumococcal

  18. Dilute Group III-V nitride intermediate band solar cells with contact blocking layers

    DOEpatents

    Walukiewicz, Wladyslaw [Kensington, CA; Yu, Kin Man [Lafayette, CA

    2012-07-31

    An intermediate band solar cell (IBSC) is provided including a p-n junction based on dilute III-V nitride materials and a pair of contact blocking layers positioned on opposite surfaces of the p-n junction for electrically isolating the intermediate band of the p-n junction by blocking the charge transport in the intermediate band without affecting the electron and hole collection efficiency of the p-n junction, thereby increasing open circuit voltage (V.sub.OC) of the IBSC and increasing the photocurrent by utilizing the intermediate band to absorb photons with energy below the band gap of the absorber layers of the IBSC. Hence, the overall power conversion efficiency of a IBSC will be much higher than an conventional single junction solar cell. The p-n junction absorber layers of the IBSC may further have compositionally graded nitrogen concentrations to provide an electric field for more efficient charge collection.

  19. Dilute group III-V nitride intermediate band solar cells with contact blocking layers

    DOEpatents

    Walukiewicz, Wladyslaw; Yu, Kin Man

    2015-02-24

    An intermediate band solar cell (IBSC) is provided including a p-n junction based on dilute III-V nitride materials and a pair of contact blocking layers positioned on opposite surfaces of the p-n junction for electrically isolating the intermediate band of the p-n junction by blocking the charge transport in the intermediate band without affecting the electron and hole collection efficiency of the p-n junction, thereby increasing open circuit voltage (V.sub.OC) of the IBSC and increasing the photocurrent by utilizing the intermediate band to absorb photons with energy below the band gap of the absorber layers of the IBSC. Hence, the overall power conversion efficiency of a IBSC will be much higher than an conventional single junction solar cell. The p-n junction absorber layers of the IBSC may further have compositionally graded nitrogen concentrations to provide an electric field for more efficient charge collection.

  20. Group-V intermixing in InAs/InP quantum dots

    SciTech Connect

    Chia, C.K.; Chua, S.J.; Tripathy, S.; Dong, J.R.

    2005-01-31

    Postgrowth intermixing in InAs/InP quantum dot (QD) structures have been investigated by rapid thermal annealing and laser irradiation techniques. In both cases, room-temperature photoluminescence (PL) measured from the QD structures after intermixing shows a substantial blueshift accompanied by an improvement in PL intensity and a reduction in linewidth. In the case of impurity free vacancy disordering, an energy shift of up to 350 meV has been achieved. The maximum differential energy shift for samples capped with SiO{sub 2} and SiN{sub x} dielectrics was found to be 90 meV. On the other hand, laser-induced intermixing allows differential energy shifts of more than 250 meV in this material system. Micro-Raman measurement shows the appearance of InAs-type and InP-type optical phonon peaks from laser-annealed InAs/InP QDs due to the exchange of As and P at the QD interfaces.

  1. Description of the first disc Δ1(t) of the commuting graph C(G, X) for elements of order three in symmetric groups

    NASA Astrophysics Data System (ADS)

    Nawawi, Athirah; Rowley, Peter

    2016-06-01

    The commuting graph C(G, X), where G is a finite group and X is a subset of G, is the graph whose vertex set is X and two distinct elements of X being joined by an edge whenever they commute in the group G. Here the CG(t)-orbit representatives and the number of elements in the first disc Δ1(t) of C(G, X), is studied when G is a symmetric group of degree n, Sym(n) and X is a conjugacy class of elements of order three.

  2. [Study on the infrared spectra of metallic clusters containing R2dtc ligand and V = O group].

    PubMed

    Zhu, H; Chen, C; Yang, Y; Deng, Y; Zhang, Y; Liu, Q

    2000-12-01

    This paper reports the features and regularities of the infrared spectra for two kinds of complexes containing R2dtc ligand. The cubane-like clusters containing R2dtc ligand possess weak and wide peaks at 400-500 cm-1 assigned to M-mu 3S vibration, while the peaks at 330-380 cm-1 and 1,470-1,510 cm-1 can be assigned to M-Sdtc and C-N vibrations, respectively. The nu(C-N) and nu(C = S) vibrations for Me2dtc-cubane cluster exhibit blue shift and red shift, respectively, when compared with those of other R2dtc ones. This would be attributed to the strong super-conjugation of the methyl group. The M-mu 3S vibrations for both types of complexes [V2Cu2S4(R2dtc)2(PhS)2]2- and [VCu4S4(R2dtc)n(PhS)4-n]3- (n = 0, 1, 2) occur at 480 and 465 cm-1, respectively. This small difference becomes a useful indication to distinguish the two types of clusters. Cluster complexes containing (R2dtc)2V2O2(mu-S)2 structural unit show the V = O vibration in the range of 844-970 cm-1. It is noted that (Et4N)[V3S2O3(Et2dtc)3] contains two sets of the V = O bonds corresponding to two sets of V = O vibrations at 970 and 844 cm-1. An additional coordination of the V = O bond to another metal atom obviously weakens the V = O bond to give rise to the red shift of the infrared frequency. Similar red shifts were also observed for other complexes and were discussed.

  3. Partitioning of platinum-group elements and Au between sulfide liquid and basalt and the origins of mantle-crust fractionation of the chalcophile elements

    NASA Astrophysics Data System (ADS)

    Mungall, James E.; Brenan, James M.

    2014-01-01

    The partitioning of platinum-group elements (PGE; Os, Ir, Ru, Rh, Pt, and Pd) and Au between sulfide melt and silicate melt (i.e., DPGEsul) exerts a critical control on the PGE composition of the Earth’s crust and mantle, but previous estimates have been plagued by experimental uncertainties and vary through several orders of magnitude. Here we present direct experimental measurements of DPGEsul, based on in situ microanalysis of the sulfide and silicate melt, with values ranging from ∼4 × 105 (Ru) to ∼2-3 × 106 (Ir, Pt). Our measurements of DPGEsul are >100 times larger than previous results but smaller than anticipated based on comparison of alloy solubilities in sulfide melts and S-free silicate melts. The presence of S in the silicate melt greatly increases alloy solubility. We use our new set of partition coefficients to develop a fully constrained model of PGE behavior during melting which accurately predicts the abundances of PGE in mantle-derived magmas and their restites, including mid-ocean ridge basalts, continental picrites, and the parental magmas of the Bushveld Complex of South Africa. Our model constrains mid-ocean ridge basalt (MORB) to be the products of pooled low and high degree fractional melts. Within-plate picrites are pooled products of larger degrees of fractional melting in columnar melting regimes. A significant control on PGE fractionation in mantle-derived magmas is exerted by residual alloy or platinum group minerals in their source. At low pressures (e.g., MORB genesis) the mantle residual to partial melting retains primitive mantle inter-element ratios and abundances of PGE until sulfide has been completely dissolved but then evolves to extremely high Pt/Pd and low Pd/Ir because Pt and Ir alloys form in the restite. During melting at high pressure to form picrites or komatiites Ir alloy appears as a restite phase but Pt alloy is not stable due to the large effect of pressure on fS2, and of temperature on fO2 along an internal

  4. Element distribution patterns in the ordovician Galena group, Southeastern Minnesota: Indicators of fluid flow and provenance of terrigenous material

    USGS Publications Warehouse

    Lively, R.S.; Morey, G.B.; Mossler, J.H.

    1997-01-01

    As part of a regional geochemical investigation of lower Paleozoic strata in the Hollandale embayment of southeastern Minnesota, elemental concentrations in acid-insoluble residues were determined for carbonate rock in the Middle Ordovician Galena Group. Elemental distribution patterns within the insoluble residues, particularly those of Ti, Al, and Zr, show that the Wisconsin dome and the Wisconsin arch, which contributed sediment to the embayment prior to Galena time, continued as weak sources of sediment during this period. In contrast, trace metals commonly associated with Mississippi Valley-type lead-zinc mineralization, including Pb, Zn, Cu, Ag, Ni, Co, As, and Mo, show dispersal patterns that are independent of those associated with primary depositional phenomena. These trace metals are concentrated in southern Minnesota in carbonate rocks near the interface between limestone- and dolostone-dominated strata. Dispersal patterns imply that the metals were carried by a north-flowing regional ground-water system. The results show that the geochemical attributes of insoluble residues can be used to distinguish provenance and transport directions of primary sediments within a depositional basin from effects of subsequent regional ground-water flow systems.

  5. Batch leaching tests of motherboards to assess environmental contamination by bromine, platinum group elements and other selected heavy metals.

    PubMed

    Almeida, César; Grosselli, Melina; González, Patricia; Martínez, Dante; Gil, Raúl

    2016-02-01

    In this study, a batch leaching test was executed to evaluate the toxicity associated with chemicals contained in motherboards. The leaching solutions used were distilled water, nitric acid, acetic acid and synthetic acid rain solution. A total of 21 elements including Ag, As, Au, Br, Cd, Co, Cr, Cu, Hf, Ir, Mn, Ni, Os, Pb, Pd, Pt, Rd, Rh, Se, U and Zn were analyzed. In this study, the pH values of all the leachates fell within the range of 2.33-4.88. The highest concentrations of metals were obtained from the acid rain solution, whilst the maximum value of bromine was achieved with solution of acetic acid. Appreciable concentrations of platinum group elements were detected with concentrations around 3.45, 1.43, 1.21 and 22.19 µg L(-1) for Ir, Pd, Pt and Rh, respectively. The different leaching of the motherboards revealed the predominant presence of the toxic substances in the leached from the e-waste.

  6. Alteration of platinum-group minerals and dispersion of platinum-group elements during progressive weathering of the Aguablanca Ni-Cu deposit, SW Spain

    NASA Astrophysics Data System (ADS)

    Suárez, Saioa; Prichard, Hazel M.; Velasco, Francisco; Fisher, Peter C.; McDonald, Iain

    2010-04-01

    The distribution, mineralogy and mobility of the platinum-group elements (PGE) in the surface environment are poorly understood. This study of the lower, less altered and upper, more altered gossan, overlying the Aguablanca Ni-Cu-(PGE) magmatic deposit (Spain), has shown that the platinum-group minerals (PGM) are progressively oxidised and dispersed into iron oxides that form the gossan. A combination of the characterization of PGE in host PGM, using a scanning electron microscope, and measurement of PGE at lower concentrations in host iron oxides, using laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS), has for the first time allowed the total distribution of the PGE within a gossan to be documented. This study has revealed a complete in situ alteration and dispersion sequence of the PGM including (1) breakdown of both the more stable Pt-arsenides, Pt/Pd-tellurides and the less stable bismuthotellurides, (2) formation of partially oxidised PGM, (3) development of a wide range of oxidised Pt- and Pd-bearing phases, (4) subsequent formation of Fe-PGE-oxides and PGE-hydroxides, (5) incorporation of PGE into ferruginous supergene products and lastly (6) concentration of PGE at the edges of veins and iron oxides. Dispersion of Pd is greater than for the other PGE with Pd being widely distributed throughout the iron oxides. This oxidising environment produced PGE-oxides rather than PGE-alloys, also commonly found in the surface environment, especially in placers. These results provide critical evidence for the stages of mineralogical change from PGE host mineralogy in magmatic ores to surface weathering producing PGE-oxides.

  7. First-principles study of high temperature and high-pressure behavior of carbides and nitrides of group IVB elements

    NASA Astrophysics Data System (ADS)

    Mishra, Vinayak; Chaturvedi, Shashank

    2016-01-01

    Full potential linearized augmented plane wave method combined with quasi-harmonic approximation, has been used to perform the calculations of thermophysical properties of carbides and nitrides of the group IVB elements at high temperature and pressure. Relative accuracy of linear density approximation (LDA) and generalized gradient approximation (GGA) exchange correlation potentials have been tested. Specific heat (?) obtained through LDA and GGA agrees with experimental data up to 1500 K. Above 1500 K, GGA gives better agreement whereas LDA under-estimates the specific heat. LDA overestimates the bulk modulus, GGA gives better agreement with the experimental data. High-temperature bulk modulus follows the Wachtman formula. Calculated ? isotherms agree with published experimental results. The transformation pressures (?) from NaCl-type structure (B? phase) to CsCl-type structure (B? phase), and collapsed volumes (?) at (?) have been predicted. The stability and hardness of these compounds are related with the calculated density of states.

  8. Platinum-group elements in rocks from the voikar-syninsky ophiolite complex, Polar Urals, U.S.S.R.

    USGS Publications Warehouse

    Page, N.J.; Aruscavage, P. J.; Haffty, J.

    1983-01-01

    Analyses of platinum-group elements (PGE) in rocks collected from the Voikar-Syninsky ophiolite in the Polar Urals suggest that the distribution and geochemistry of PGE in this Paleozoic ophiolite are similar to those in Mesozoic ophiolites from elsewhere. Chondrite-normalized PGE patterns for chromitite, the tectonite unit, and ultramafic and mafic cumulate unit have negative slopes. These results are similar to those found for chromitites from other ophiolites; stratiform chromities show positive slopes. If the magmas that form both types of chromitite originate from similar mantle source material with respect to PGE content, the processes involved must be quite different. However, the distinct chondrite-normalized PGE patterns may reflect differing source materials. ?? 1983 Springer-Verlag.

  9. Les Houches Physics at TeV Colliders 2005 Beyond the Standard Model Working Group: Summary Report

    SciTech Connect

    Allanach, B.C.; Grojean, C.; Skands, P.; Accomando, E.; Azuelos, G.; Baer, H.; Balazs, C.; Belanger, G.; Benakli, K.; Boudjema, F.; Brelier, B.; Bunichev, V.; Cacciapaglia, G.; Carena, M.; Choudhury, D.; Delsart, P.-A.; De Sanctis, U.; Desch, K.; Dobrescu, B.A.; Dudko, L.; El Kacimi, M.; /Saclay, SPhT /CERN /Fermilab /INFN, Turin /Turin U. /Montreal U. /TRIUMF /Florida State U. /Argonne /Annecy, LAPTH /Paris, LPTHE /Moscow State U. /Cornell U., CIHEP /Delhi U. /Milan U. /INFN, Milan /Freiburg U. /Cadi Ayyad U., Marrakech /Orsay, LPT /Oslo U. /Lancaster U.

    2006-03-17

    The work contained herein constitutes a report of the ''Beyond the Standard Model'' working group for the Workshop ''Physics at TeV Colliders'', Les Houches, France, 2-20 May, 2005. We present reviews of current topics as well as original research carried out for the workshop. Supersymmetric and non-supersymmetric models are studied, as well as computational tools designed in order to facilitate their phenomenology.

  10. Does Project L.I.V.E. Case Modality Impact Critical Thinking in PBL Groups?

    ERIC Educational Resources Information Center

    Kamin, Carol; O'Sullivan, Patricia; Deterding, Robin

    Problem-based learning (PBL) with simulated cases is one method of delivering standardized pediatric curricular objectives, but the fact that students are dispersed and participating in community-based practices makes group meetings difficult. To address these issues, researchers developed and tested a new modality for presenting PBL cases, a…

  11. Antibacterial activity of microstructured sacrificial anode thin films by combination of silver with platinum group elements (platinum, palladium, iridium).

    PubMed

    Köller, Manfred; Bellova, Petri; Javid, Siyamak Memar; Motemani, Yahya; Khare, Chinmay; Sengstock, Christina; Tschulik, Kristina; Schildhauer, Thomas A; Ludwig, Alfred

    2017-05-01

    Five different Ag dots arrays (16 to 400dots/mm(2)) were fabricated on a continuous platinum, palladium, or iridium thin film and for comparison also on titanium film by sputter deposition and photolithographic patterning. To analyze the antibacterial activity of these microstructured films Staphylococcus aureus (S. aureus) were placed onto the array surfaces and cultivated overnight. To analyze the viability of planktonic as well as surface adherent bacteria, the applied bacterial fluid was subsequently aspirated, plated on blood agar plates and adherent bacteria were detected by fluorescence microscopy. A particular antibacterial effect towards S. aureus was induced by Ag dot arrays on each of the platinum group thin film (sacrificial anode system for Ag) in contrast to Ag dot arrays fabricated on the Ti thin films (non-sacrificial anode system for Ag). Among platinum group elements the Ir-Ag system exerted the highest antibacterial activity which was accompanied by most advanced dissolution of the Ag dots and Ag ion release compared to Ag dots on Pt or Pd.

  12. Major and trace element composition of copiapite-group minerals and coexisting water from the Richmond mine, Iron Mountain, California

    USGS Publications Warehouse

    Jamieson, H.E.; Robinson, C.; Alpers, C.N.; McCleskey, R.B.; Nordstrom, D.K.; Peterson, Ronald C.

    2005-01-01

    Copiapite-group minerals of the general formula AR4 (SO4)6(OH)2??nH2O, where A is predominantly Mg, Fe2+, or 0.67Al3+, R is predominantly Fe3+, and n is typically 20, are among several secondary hydrous Fe sulfates occurring in the inactive mine workings of the massive sulfide deposit at Iron Mountain, CA, a USEPA Superfund site that produces extremely acidic drainage. Samples of copiapite-group minerals, some with coexisting water, were collected from the Richmond mine. Approximately 200 mL of brownish pore water with a pH of -0.9 were extracted through centrifugation from a 10-L sample of moist copiapite-group minerals taken from pyritic muck piles. The pore water is extremely rich in ferric iron (Fe3+=149 g L-1, FeT=162 g L-1 and has a density of 1.52 g mL-1. The composition of the pore water is interpreted in the context of published phase relations in the Fe2O3- SO3-H2O system and previous work on the chemistry of extremely acid mine waters and associated minerals in the Richmond mine. Two distinct members of the copiapite mineral group were identified in the samples with coexisting water: (1) abundant magnesiocopiapite consisting of platy crystals 10 to 50 ??m and (2) minor aluminocopiapite present as smaller platy crystals that form spheroidal aggregates. The average composition (n=5) of the magnesiocopiapite is (Mg0.90Fe0.172+ Zn0.02Cu0.01)???1.10(Fe3.833+Al0.09)???3.92(SO4) 6.00(OH)1.96??20H2O. Bulk compositions determined by digestion and wet-chemical analysis are consistent with the microanalytical results. These results suggest that magnesiocopiapite is the least soluble member of the copiapite group under the prevailing conditions. Micro-PIXE analysis indicates that the copiapite-group minerals in this sample sequester Zn (average 1420 ppm), with lesser amounts of Cu (average 270 ppm) and As (average 64 ppm). ?? 2004 Elsevier B.V. All rights reserved.

  13. Porous Silica Sol-Gel Glasses Containing Reactive V2O5 Groups

    NASA Technical Reports Server (NTRS)

    Stiegman, Albert E.

    1995-01-01

    Porous silica sol-gel glasses into which reactive vanadium oxide functional groups incorporated exhibit number of unique characteristics. Because they bind molecules of some species both reversibly and selectively, useful as chemical sensors or indicators or as scrubbers to remove toxic or hazardous contaminants. Materials also oxidize methane gas photochemically: suggests they're useful as catalysts for conversion of methane to alcohol and for oxidation of hydrocarbons in general. By incorporating various amounts of other metals into silica sol-gel glasses, possible to synthesize new materials with broad range of new characteristics.

  14. Platinum group and chalcophile element systematics of serpentinized peridotites from the St. Elena ophiolite in Costa Rica

    NASA Astrophysics Data System (ADS)

    Holm, J.; Bizimis, M.; Schwarzenbach, E. M.; Foustoukos, D.; Frisby, C. P.; Brandon, A. D.; Gazel, E.

    2015-12-01

    We present in situ LA-ICPMS data on platinum group element (PGE) and chalcophile element (namely Cu, Ag, Te, Au, Pb) systematics in sulfides from partially serpentinized peridotites of the St. Elena ophiolite, Costa Rica. PGE are strong indicators of primary mantle processes, though their behavior during low temperature alteration processes such as serpentinization is not well understood. St. Elena sulfides are dominantly pentlandites that coexist with Fe-Ni alloys and native Cu. This indicates extremely low fO2 and fS2 conditions likely established during the early stages of serpentinization. We observe extremely variable PGE-Re concentrations in the sulfides, (e.g. [Os] = 2 - 100,000 times primitive mantle, PM). Low [Os] sulfides have high Pd/Os, which in turn correlates positively with Cu concentrations, suggesting Pd enrichment through Cu-rich fluids (e.g. Schwarzenbach et al., 2014, CMP) as opposed to melt-rock reaction. Sulfide PM-normalized PGE-Re patterns are dominated by strong Pt depletions (e.g., Pt/Pd = 0.80-0.0009). Occasional Pt enrichments over Pd and Ru (or Rh) in a PM-normalized pattern (~5% of the sulfide population) often correlate with Te and/or Au enrichments. Pt enrichment was also observed in a composite pentlandite-awaruite, suggesting possible exsolution of Pt from sulfides under extremely low fS2 conditions. Pb concentrations do not correlate with other chalcophiles or PGE. Pb ranges from 0.01-31.64 ppm with the majority of sulfides <5 ppm, and an average concentration of 2.77 ppm (n=64). Assuming that this Pb concentration is representative of mantle sulfides, this implies that Pb is not dominantly held in sulfides in the upper mantle. Combination of in situ and bulk rock PGE analyses will be used to distinguish the effects of primary magmatic signatures (e.g., melt depletion, melt-rock interaction) and secondary processes such as serpentinization on the PGE-Re and chalcophile element systematics of these sulfides.

  15. Conservation of an Actinomyces viscosus T14V type 1 fimbrial subunit homolog among divergent groups of Actinomyces spp.

    PubMed Central

    Yeung, M K

    1992-01-01

    The type 1 fimbrial subunit gene of the human Actinomyces viscosus T14V was used as a DNA probe in Southern analyses to detect related DNA sequences in 16 of 30 strains of Actinomyces spp. under conditions of high stringency. The organisms with homology to the DNA probe included two human and six nonhuman A. viscosus, three human and three nonhuman A. naeslundii, and two A. bovis isolates. Homologous DNA sequences were not detected in strains of A. odontolyticus and A. israelii examined in this study. Northern (RNA) blot analysis revealed expression of a transcript from each of the A. viscosus and A. naeslundii strains and from one A. bovis strain that was comparable in size to that detected from A. viscosus T14V. Cell surface fimbriae were observed on a majority of the strains that expressed the transcript. Various degrees of cross-immunoreactivities between these strains and antibodies specific for type 1 fimbriae of A. viscosus T14V were also observed by colony immunoassay. Thus, the data clearly demonstrate the existence in, and expression by, divergent Actinomyces groups of genomic sequences that are closely related to the type 1 fimbriae of A. viscosus T14V. Images PMID:1347285

  16. Novel insertion sequence-like elements in phytoplasma strains of the aster yellows group are putative new members of the IS3 family.

    PubMed

    Lee, I-M; Zhao, Y; Bottner, K D

    2005-01-15

    Novel insertion sequence (IS)-like elements were isolated and characterized from phytoplasma strains in the aster yellows (AY) group (16SrI). The IS-like elements were cloned from phytoplasma strains AY1 and NJAY or PCR-amplified from 15 additional strains representing nine subgroups in the AY group using primers based on sequences of the putative transposases (Tpases). All IS-like elements contained sequences encoding similar Tpases of 321 amino acids (320 for strain CPh). Substantial amino acid sequence variability suggested multiple species of Tpases or IS-like elements exist in the AY phytoplasma group. These Tpases have an identical DDE motif that is most similar to the DDE consensus of Tpases in the IS3 family.

  17. Structural environments of incompatible elements in silicate glass/melt systems: II. U IV, U V, and U VI

    NASA Astrophysics Data System (ADS)

    Farges, Franã§Ois; Ponader, Carl W.; Calas, Georges; Brown, Gordon E., Jr.

    1992-12-01

    The structural environments of trace to minor levels (≈2000 ppm to ≈3.0 wt%) of U in several silicate glasses were examined as a function of oxygen fugacity, melt composition, and melt polymerization using X-ray (XANES and EXAFS) and optical absorption spectroscopies. Glass compositions were diopside (CaMgSi 2O 6: DI), anorthite (CaAlSi 2O 8: AN), albite (NaAlSi 3O 8: AB), sodium trisilicate (Na 2Si 3O 7: TS), a peralkaline composition (Na 3.3AlSi 7O 17: PR, approximately halfway between AB and TS), and a calc-alkaline rhyolite composition (RH). A second set of silicate glasses of the same base compositions containing ≈2000 ppm to ≈3.0 wt% U and ≈0.6 to 2.5 wt% F or Cl was also synthesized. In the glasses synthesized under oxidizing conditions (in air), U VI occurs as uranyl groups with two axial oxygens at ≈ 1.77-1.85 ± 0.02 Å and four to five equatorial oxygens at ≈2.21-2.25 ± 0.03 Å. In glasses synthesized under more reducing conditions ( fO2 ≈ 10 -3-10 -7 atm), U V occurs in moderately distorted 6-coordinated polyhedra [ d(U V-O) ≈ 2.19-2.24 ± 0.03 Å], which may co-exist with smaller numbers of U VI species and/or U VI species. Under the most reducing conditions used ( fO2 ≈ 10 -8-10 -12 atm), U IV occurs in less distorted octahedra [ d(U IV-O) ≈ 2.26-2.29 ± 0.02 Å]. No clear evidence for U-F or U-Cl bonds was found for any of the halogen-containing glasses, suggesting that U-halogen "complexes" are not present. In addition, no U-U (second-neighbor) interactions were detected, indicating that no significant clustering of U atoms is present in any of the glasses studied. Bond strength-bond length calculations and constraints placed on local bonding by Pauling's second rule suggest that U IV and U V in 6-coordinated sites in silicate melts will preferentially bond to nonbridging oxygens (NBO's) rather than bridging oxygens (BO's). The unusually low 6-fold coordination of U IV and U V in relatively depolymerized silicate melts (e

  18. Fossil group origins. V. The dependence of the luminosity function on the magnitude gap

    NASA Astrophysics Data System (ADS)

    Zarattini, S.; Aguerri, J. A. L.; Sánchez-Janssen, R.; Barrena, R.; Boschin, W.; del Burgo, C.; Castro-Rodriguez, N.; Corsini, E. M.; D'Onghia, E.; Girardi, M.; Iglesias-Páramo, J.; Kundert, A.; Méndez-Abreu, J.; Vilchez, J. M.

    2015-09-01

    Context. In nature we observe galaxy aggregations that span a wide range of magnitude gaps between the two first-ranked galaxies of a system (Δm12). Thus, there are systems with gaps close to zero (e.g., the Coma cluster), and at the other extreme of the distribution, the largest gaps are found among the so-called fossil systems. The observed distribution of magnitude gaps is thought to be a consequence of the orbital decay of M∗ galaxies in massive halos and the associated growth of the central object. As a result, to first order the amplitude of this gap is a good statistical proxy for the dynamical age of a system of galaxies. Fossil and non-fossil systems could therefore have different galaxy populations that should be reflected in their luminosity functions. Aims: In this work we study, for the first time, the dependence of the luminosity function parameters on Δm12 using data obtained by the fossil group origins (FOGO) project. Methods: We constructed a hybrid luminosity function for 102 groups and clusters at z ≤ 0.25 using both photometric data from the SDSS-DR7 and redshifts from the DR7 and the FOGO surveys. The latter consists of ~1200 new redshifts in 34 fossil system candidates. We stacked all the individual luminosity functions, dividing them into bins of Δm12, and studied their best-fit Schechter parameters. We additionally computed a "relative" luminosity function, expressed as a function of the central galaxy luminosity, which boosts our capacity to detect differences - especially at the bright end. Results: We find trends as a function of Δm12 at both the bright and faint ends of the luminosity function. In particular, at the bright end, the larger the magnitude gap, the fainter the characteristic magnitude M∗. The characteristic luminosity in systems with negligible gaps is more than a factor three brighter than in fossil-like ones. Remarkably, we also find differences at the faint end. In this region, the larger the gap, the flatter

  19. Separating Continental Mineral Dust from Cosmic Dust using Platinum Group Element Concentrations and Osmium Isotopes in Ancient Polar Ice

    NASA Astrophysics Data System (ADS)

    Seo, J. H.; Jackson, B.; Osterberg, E. C.; Sharma, M.

    2015-12-01

    The platinum group element (PGEs: Pt, Pd, Rh, Ir, Os, and Ru) accumulation in ancient polar archives have been argued to trace cosmic dust and "smoke" from larger meteors but the PGE concentration data lack specificity. For example, the extent to which the terrestrial volcanism/dust has contributed to the PGE inventory of polar ice cannot be readily evaluated. Since the Os isotope compositions (187Os/188Os ratio) of the terrestrial and extraterrestrial sources are distinctly different from each other, the PGE concentrations when combined with Os isotope composition have the potential to untangle contributions from these sources. Platinum group element concentration determinations in polar ice cores are highly challenging due to their extremely low concentrations (down to 10-15 g/g or fg/g). Here, a new procedure is presented that allows PGEs and Os isotope compositions to be determined from a ~50 g sample of polar ice. Decontaminated ice-melt is spiked with 101Ru, 106Pd, 190Os, 191Ir, and 198Pt and frozen at -20 °C in quartz-glass ampoules. A mixture of purified HNO3 and H2O2 is then added and the sample is heated to 300 °C at 128bar using a High Pressure Asher. This allows all spikes to be equilibrated with the sample PGEs and all Os species are oxidized to OsO4. The resulting OsO4 is extracted using distillation, purified, and measured using negative thermal ionization mass spectrometry. PGEs are then separated and purified using two stage column chromatography and their concentrations determined by isotope dilution using a triple quadruople inductively coupled plasma mass spectrometer coupled to an Apex de-solvation nebulizer. The developed method was applied to modern Greenland firn and snow. The PGE concentrations of the firn are 4.0 fg/g for Ir, 20 fg/g for Ru, 590 fg/g for Pt, 38 fg/g for Pd, and 1.3 fg/g for Os, while those of the snow are 3.0 fg/g for Ir, 53 fg/g for Ru, 360 fg/g for Pt, 32 fg/g for Pd, and 0.4 fg/g for Os, respectively. A comparison

  20. Response evaluation criteria for solid tumours in dogs (v1.0): a Veterinary Cooperative Oncology Group (VCOG) consensus document.

    PubMed

    Nguyen, S M; Thamm, D H; Vail, D M; London, C A

    2015-09-01

    In veterinary medical oncology, there is currently no standardized protocol for assessing response to therapy in solid tumours. The lack of such a formalized guideline makes it challenging to critically compare outcome measures across various treatment protocols. The Veterinary Cooperative Oncology Group (VCOG) membership consensus document presented here is based on the recommendations of a subcommittee of American College of Veterinary Internal Medicine (ACVIM) board-certified veterinary oncologists. This consensus paper has used the human response evaluation criteria in solid tumours (RECIST v1.1) as a framework to establish standard procedures for response assessment in canine solid tumours that is meant to be easy to use, repeatable and applicable across a variety of clinical trial structures in veterinary oncology. It is hoped that this new canine RECIST (cRECIST v1.0) will be adopted within the veterinary oncology community and thereby facilitate the comparison of current and future treatment protocols used for companion animals with cancer.

  1. Structures and Mechanical and Electronic Properties of the Ti2CO2 MXene Incorporated with Neighboring Elements (Sc, V, B and N)

    NASA Astrophysics Data System (ADS)

    Feng, Li; Zha, Xian-Hu; Luo, Kan; Huang, Qing; He, Jian; Liu, Yijun; Deng, Wei; Du, Shiyu

    2017-04-01

    Ti2CO2, as the representative MXene with semiconducting characteristics and ultrahigh carrier mobility, has attracted increasing attention in material science. Herein, various Ti2CO2 alloys with Ti displaced by neighboring elements Sc and V, or C by B and N are investigated in this paper based on the first-principles density functional calculations. The structures and mechanical and electronic properties are thoroughly studied for the configurations with varying alloying atom concentrations. The choices of alloying elements play a critical role in determining the lattice parameters and layer thickness. The Sc substitutions generally increase the lattice parameter but decrease the layer thickness. In contrast, the introduction of N presents slight influence on the structural parameters. The mechanical strength shows remarkable variations by introducing the alloying elements. The maximum elastic constant c 11 is determined to be 425 GPa in (Ti0.25V0.75)2CO2, and the corresponding minimum value is only 104 GPa found in (Ti0.125Sc0.875)2CO2. With respect to the electronic properties, although B and Sc both present one less valance electron compared to their replaced elements C and Ti, it is easier to realize the p-type semiconductor in the configurations containing Sc. Both the V and N substitutions are capable of generating n-type semiconductors, but their optimal stoichiometric compositions are quite different. Among all the configurations investigated, only (Ti0.5V0.5)2CO2 and (Ti0.375V0.625)2CO2 are magnetic, with their magnetism determined to be 2.61 uB/cell and 1.52 uB/cell, respectively. Thus, the method of alloying neighboring elements provides an effective approach in manipulating the physical properties of the Ti2CO2, which might widen the possible applications of MXene materials.

  2. The effects of group-I elements co-doping with Mn in ZnO dilute magnetic semiconductor

    NASA Astrophysics Data System (ADS)

    Zhang, Liqiang; Zhang, Yinzhu; Ye, Zhizhen; Lu, Jianguo; Lu, Bin; He, Bo

    2012-06-01

    Mn-Li codoped ZnO (Zn(Mn,Li)O), Mn-Na codoped ZnO (Zn(Mn,Na)O), and Mn-K codoped ZnO (Zn(Mn,K)O) thin films were deposited on quartz substrates by pulsed laser deposition. The doping effects of group-I elements (e.g., Li, Na, and K) on the structural, magnetic, and optical properties of the Mn doped ZnO (ZnMnO) films were discussed. X-ray diffraction and K-edge x-ray absorption near-edge structure measurements revealed that all the films showed a hexagonal wurtzite ZnO structure, and no other clusters, precipitates, or second phases were detected. Zn(Mn,Na)O and Zn(Mn,Li)O films showed a weak p-type conductivity, while the Zn(Mn,K)O film appeared a highly resistivity. The saturation magnetization of Zn(Mn,Na)O and Zn(Mn,Li)O films was 1.2 and 0.18 μB/Mn, respectively. The hole-related defects, induced by doping with a low content of Li or Na, contributed to the room temperature ferromagnetism in the ZnMnO system.

  3. Thermal Evaporation Synthesis and Properties of ZnO Nano/Microstructures Using Carbon Group Elements as the Reducing Agents.

    PubMed

    Lv, H; Sang, Dd; Li, Hd; Du, Xb; Li, Dm; Zou, Gt

    2010-01-21

    ZnO nano/microstructures have been formed by thermal evaporation method using ZnO powders mixed with carbon group elements (C, Si, Ge, Sn, or Pb) as the reducing agent. For cases of mixed precursors of ZnO/C, ZnO/Si, and ZnO/Ge, the pure ZnO nano/microstructures are realized, while for ZnO/Sn (ZnO/Pb) systems, the phase of Pb2O3(Zn2SnO4) generally are represented in the ZnO products. The appearance of Pb2O3(Zn2SnO4) is attributed to the lower melting point and higher vapor pressure of Sn (Pb) in the heating and evaporation processes. The morphologies and sizes of the products are controlled by adjusting the growth regions and/or introducing gaseous argon. Room temperature (RT) photoluminescence spectra indicate that the intensity (peak position) of the ultraviolet emission is increased (redshift) due to the existence of Zn2SnO4 phase in the ZnO products. The Pb2O3(Zn2SnO4) phase in ZnO nano/microstructures plays a important role in enhancing the saturation magnetizations of RT ferromagnetism with respect to the case of pure ZnO products fabricated by the precursor of mixed ZnO and graphite.

  4. Rare earth element migration in gullies with different Dicranopteris dichotoma covers in the Huangnikeng gully group, Changting County, Southeast China.

    PubMed

    Chen, Zhiqiang; Chen, Zhibiao; Bai, Liyue

    2016-12-01

    Little is known about rare earth element (REE) migration in gullies in Southeast China. We examine the concentration and distribution of REE, soil variables, and correlations among REE and soil variables field investigation, laboratory measurement, and statistical analysis in the three gullies with different Dicranopteris dichotoma covers in the Huangnikeng gully group, Changting County, Southeast China. We show that the REE pattern in gullies is typical of red soil in Southeast China. REE migrate severely in gullies with low vegetation cover, REE migrate from higher sites to lower sites under the influence of water flow and gravity, and gullies can be considered an important REE source. Dicranopteris dichotoma can succeed in gullies and affect part of soil variables, organic C and pH can play an important role in REE migration in gullies, and Dicranopteris dichotoma is a recommended plant for effectively controlling REE migration and gully erosion. The critical vegetation cover of gullies should be further studied to control REE migration and gully erosion.

  5. Platinum group element enrichments and possible chondritic Ru:Ir across the Frasnian-Famennian boundary, western New York State.

    PubMed

    Over, D J; Conaway, C A; Katz, D J; Goodfellow, W D; Gregoire, D C

    1997-08-01

    The Frasnian-Famennian boundary is recognized as the culmination of a global mass extinction in the Late Devonian. In western New York State the boundary is a distinct horizon within a pyritic black shale bed of the upper Hanover Shale defined by the first occurrence of Palmatolepis triangularis in the absence of Frasnian conodonts. The boundary is characterized by a minor disconformity marked by a lag concentration of conodonts. Iridium at the boundary is 0.11-0.24 ng/g, two to five times background levels of <0.05 ng/g; other Ir enrichments of 0.38 ng/g and 0.49 ng/g occur within 50 cm of the conodont-constrained boundary. Numerous Ir enrichments in the boundary interval suggest extraterrestrial accretion and platinum group element (PGE) concentration at disconformities, or mobilization and concentration in organic-rich/pyritic-rich laminations from cosmic or terrestrial sources. PGE ratios of Pt/Pd and Ku/Ir at the boundary horizon approximate chondritic ratios and are suggestive of an unaltered extraterrestrial source. These values do not conclusively establish a single extraterrestrial impact as the ultimate cause of the Frasnian-Famennian mass extinction, especially given the presence of similar Ir enrichments elsewhere in the section and the absence at the boundary of microtektites and shocked mineral grains.

  6. Accumulation of germanium and rare earth elements in functional groups of selected energy crops cultivated on two different soils

    NASA Astrophysics Data System (ADS)

    Wiche, Oliver; Székely, Balázs

    2016-04-01

    A field experiment was conducted to investigate the uptake of Ge and selected REEs in functional groups of selected crop species. Five species belonging to the functional group of grasses (Hordeum vulgare, Zea mays, Avena sativa, Panicum miliaceum and Phalaris arundinacea) and four species from the group of herbs (Lupinus albus, Lupinus angustifolius, Fagopyrum esculentum and Brassica napus) were cultivated in parallel on two soils with slightly alkaline (soil A: pH = 7.8) and slightly acidic (soil B: pH = 6.8) conditions. After harvest, concentrations of Ge, La, Nd, Gd, Er, P, Fe, Mn and Si in shoot tissues were determined with ICP-MS. Concentrations of Ge were significantly higher in grasses than in herbs. Conversely, concentrations of La and Nd were significantly higher in herbs, than in grasses. Highest concentrations were measured in Brassica napus (REEs) and Zea mays (Ge). Concentrations of Ge significantly correlated with that of Si in the shoots showing low concentrations in herbs and high concentrations in grasses, indicating a common mechanism during the uptake in grasses. Concentrations of REEs correlated significantly with that of Fe, indicating increasing concentrations of REEs with increasing concentrations of Fe. Cultivation of species on the slightly acidic soil significantly increased the uptake Ge in Lupinus albus and Phalaris arundinacea and the uptake of La and Nd in all species except of Phalaris arundinacea. This study demonstrated that commonly used field crops could be regarded as suitable candidates for a phytomining of Ge and REEs, since these species develop high yields of shoots, high concentrations of elements and are widely used in agricultural practice. Under soil conditions where bioavailability of Ge and REEs is expected to be low (soil A) accumulation can be estimated at 1.8 g/ha Ge in Z. mays and 3.7 g/ha REEs (1.5 g/ha La, 1.4 g/ha Nd, 0.6 g/ha Gd, 0.3 g/ha Er), respectively, in B. napus, assuming a constant high efficiency of

  7. Platinum-group element concentrations in pyrite from the Main Sulfide Zone of the Great Dyke of Zimbabwe

    NASA Astrophysics Data System (ADS)

    Piña, R.; Gervilla, F.; Barnes, S.-J.; Oberthür, T.; Lunar, R.

    2016-10-01

    The Main Sulfide Zone (MSZ) of the Great Dyke of Zimbabwe hosts the world's second largest resource of platinum-group elements (PGE) after the Bushveld Complex in South Africa. The sulfide assemblage of the MSZ comprises pyrrhotite, pentlandite, chalcopyrite, and minor pyrite. Recently, several studies have observed in a number of Ni-Cu-PGE ore deposits that pyrite may host significant amounts of PGE, particularly Pt and Rh. In this study, we have determined PGE and other trace element contents in pyrite from the Hartley, Ngezi, Unki, and Mimosa mines of the Great Dyke by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). Based on the textures and PGE contents, two types of pyrite can be differentiated. Py1 occurs as individual euhedral or subhedral grains or clusters of crystals mostly within chalcopyrite and pentlandite, in some cases in the form of symplectitic intergrowths, and is PGE rich (up to 99 ppm Pt and 61 ppm Rh; 1.7 to 47.1 ppm Ru, 0.1 to 7.8 ppm Os, and 1.2 to 20.2 ppm Ir). Py2 occurs as small individual euhedral or subhedral crystals within pyrrhotite, pentlandite, and less frequently within chalcopyrite and silicates and has low PGE contents (<0.11 ppm Pt, <0.34 ppm Rh, <2.5 ppm Ru, <0.37 ppm Ir, and <0.40 ppm Os). Py1 contains higher Os, Ir, Ru, Rh, and Pt contents than the associated pyrrhotite, pentlandite, and chalcopyrite, whereas Py2 has similar PGE contents as coexisting pyrrhotite and pentlandite. Based on the textural relationships, two different origins are attributed for each pyrite type. Py1 intergrowth with pentlandite and chalcopyrite is inferred to have formed by late, low temperature (<300 °C) decomposition of residual Ni-rich monosulfide solid solution, whereas Py2 is suggested to have formed by replacement of pyrrhotite and pentlandite caused by late magmatic/hydrothermal fluids.

  8. Main group tellurium heterocycles anchored by a P(2)(V)N(2) scaffold and their sulfur/selenium analogues.

    PubMed

    Nordheider, Andreas; Hüll, Katharina; Prentis, Joanna K D; Athukorala Arachchige, Kasun S; Slawin, Alexandra M Z; Woollins, J Derek; Chivers, Tristram

    2015-03-16

    A comprehensive investigation of reactions of alkali-metal derivatives of the ditelluro dianion [TePV(NtBu)(μ-NtBu)]22– (L2–, E = Te) with p-block element halides produced a series of novel heterocycles incorporating P2VN2 rings, tellurium, and group 13–16 elements. The dianion engages in Te,Te′-chelation to the metal center in Ph2Ge and R2Sn (R = tBu, nBu, Ph) derivatives; similar behavior was noted for group 14 derivatives of L2– (E = S, Se). In the case of group 13 trihalides MCl3 (M = Ga, In), neutral spirocyclic complexes (L)M[NtBu(Te)PV(μ-NtBu)2PIIIN(H)tBu)] (M = Ga, In) comprised of a Te,Te′-chelated ligand L2– and a N,Te-bonded ligand resulting from loss of Te and monoprotonation were obtained. In reactions with RPCl2 (R = tBu, Ad, iPr2N) a significant difference was observed between Se- and S-containing systems. In the former case, Se,Se′-chelated derivatives were formed in high yields, whereas the N,S-chelated isomers predominated for sulfur. All complexes were characterized by multinuclear (1H, 31P, 77Se, 119Sn, and 125Te) NMR spectroscopy; this technique was especially useful in the analysis of the mixture of (L)(Se) and (L)(SeSe) obtained from the reaction of Se2Cl2 with L2– (E = Te). Single-crystal X-ray structures were obtained for the spirocyclic In complex (9), (L)GePh2 (E = Te, 10), (L)SntBu2 (E = Te, 12a); E = Se, 12aSe, E = S, 12aS) and (L)(μ-SeSe) (E = Te, 16).

  9. T cell receptor gene usage in the response to lambda repressor cI protein. An apparent bias in the usage of a V alpha gene element

    PubMed Central

    1988-01-01

    The T cell response to the lambda repressor cI protein is directed to the same region of the protein (residues 12-26) in both BALB/c and A/J mice. A panel of T cell hybridomas specific for P12-26 in the context of either I-Ek or I-Ad have been isolated To further understand the molecular interaction between the TCR and the Ia-P12-26 complex, the primary structures of the TCR of five T cell hybridomas have been determined. Southern and Northern analyses indicate that two members of the V alpha 3 gene family are used by 13 out of 14 I-Ek-restricted T cells. Four different V beta genes are used by these T cell hybridomas, while the majority (8 out of 13) express V beta 1 in combination with the J beta 2.1 element. No clear correlation can be seen in this system between gene usage and MHC restriction. In addition, the fine specificity of I-Ek-restricted T cells to a single amino acid substitution [Phe22/His22]P12-26 is not attributed to the usage of particular V alpha and V beta elements. The V alpha 3 family gene is also used by a few I-Ad-restricted T cells. Interestingly, these I-Ad T cells share a reactivity pattern more similar to that of I-Ek- restricted T cells than other I-Ad-restricted T cells. The nonrandom selection V alpha 3 is also demonstrated by the fact that V alpha 3 is used by P12-26-specific, but not by cytochrome c- or staphylococcal nucleus-specific, I-Ek-restricted T cells. This suggests that although antigen specificity may not be accounted for by either chain of the TCR, the members of V alpha 3 genes may be selected by the antigen (P12- 26). PMID:2971753

  10. Stopping power for low-velocity heavy ions: (0-1.0)-MeV/nucleon Mg ions in 17 (Z=22-79) elemental solids

    NASA Astrophysics Data System (ADS)

    Arstila, K.; Keinonen, J.; Tikkanen, P.

    1990-04-01

    The stopping power for 24,26Mg ions in 17 (Z=22-79) elemental solids has been studied in the energy region 0-1.0 MeV/nucleon by application of the Doppler-shift attenuation method. At velocities 2v0<v<5v0 (v0 the Bohr velocity), the scaling factors 1.10 (Ti), 0.90 (V), 0.93 (Fe), 0.97 (Co), 0.99 (Ni), 1.03 (Cu), 1.05 (Ge), 1.05 (Nb), 1.15 (Mo), 1.05 (Pd), 1.08 (Ag), 1.09 (Hf), 1.07 (Ta), 1.05 (W), 1.05 (Re), 1.05 (Pt), and 0.96 (Au) to the commonly used empirical electronic stopping power by Ziegler, Biersack, and Littmark were determined to an accuracy of +/-5%. At velocities v<2v0, much higher electronic stopping power and different velocity dependence than predicted by the empirical model were obtained. The electronic stopping power was determined to an accuracy of +/-5%. The reduction of the nuclear stopping power due to the polycrystalline structure of the slowing-down materials was taken into account in the deduction of the electronic stopping power.

  11. Environmental risk of particulate and soluble platinum group elements released from gasoline and diesel engine catalytic converters.

    PubMed

    Moldovan, M; Palacios, M A; Gómez, M M; Morrison, G; Rauch, S; McLeod, C; Ma, R; Caroli, S; Alimonti, A; Petrucci, F; Bocca, B; Schramel, P; Zischka, M; Pettersson, C; Wass, U; Luna, M; Saenz, J C; Santamaría, J

    2002-09-16

    A comparison of platinum-group element (PGE) emission between gasoline and diesel engine catalytic converters is reported within this work. Whole raw exhaust fumes from four catalysts of three different types were examined during their useful lifetime, from fresh to 80,000 km. Two were gasoline engine catalysts (Pt-Pd-Rh and Pd-Rh), while the other two were diesel engine catalysts (Pt). Samples were collected following the 91441 EUDC driving cycle for light-duty vehicle testing, and the sample collection device used allowed differentiation between the particulate and soluble fractions, the latter being the most relevant from an environmental point of view. Analyses were performed by inductively coupled plasma-mass spectrometry (ICP-MS) (quadrupole and high resolution), and special attention was paid to the control of spectral interference, especially in the case of Pd and Rh. The results obtained show that, for fresh catalysts, the release of particulate PGE through car exhaust fumes does not follow any particular trend, with a wide range (one-two orders of magnitude) for the content of noble metals emitted. The samples collected from 30,000-80,000 km present a more homogeneous PGE release for all catalysts studied. A decrease of approximately one order of magnitude is observed with respect to the release from fresh catalysts, except in the case of the diesel engine catalyst, for which PGE emission continued to be higher than in the case of gasoline engines. The fraction of soluble PGE was found to represent less than 10% of the total amount released from fresh catalysts. For aged catalysts, the figures are significantly higher, especially for Pd and Rh. Particulate PGE can be considered as virtually biologically inert, while soluble PGE forms can represent an environmental risk due to their bioavailability, which leads them to accumulate in the environment.

  12. Platinum group elements in a 3. 5 Ga nickel-iron occurrence: Possible evidence of a deep mantle origin

    SciTech Connect

    Tredoux, M.; Hart, R.J.; Lindsay, N.M.; Sellschop, J.P.F. ); de Wit, M.J. Lunar and Planetary Inst., Houston, TX ); Armstrong, R.A. )

    1989-01-10

    The Bon Accord (BA) Ni-Fe deposit occurs in chemically depleted ultramafic rocks of the circa 3.5 Ga Jamestown opholite complex in the Barberton greenstone belt of the Kaapvaal craton, South Africa. BA is unusual both mineralogically and chemically. It consists of a rare Ni-rich assemblage: Ni-oxide (bunsenite), -spinels (trevorite, nichromite), and -silicates (e.g., liebenbergite, the Ni end-member olivine) and their altered equivalents. NiO (average = 38%) and FeO + Fe{sub 2}O{sub 3} (average = 34%) are the major chemical constituents. The Cu and S contents are very low (both < 100 ppm), and no evidence for replacement of preexisting sulphides has been detected. BA is enriched in platinum group elements (PGE) and shows bimodal patterns on the standard PGE diagrams. Differences between the patterns are much greater for Os and Ir than for the other PGE. This observation is interpreted as being indicative of a high-temperature process (> 2000C; lower mantle). High Ni/Fe and Ni/Co ratios (relative to C-1 chondrite) suggest that BA might have been derived form siderophile-rich material that remained in the lower mantle after inefficient core formation. A model is presented wherein such a metal-silicate heterogeneity is fractionated and oxidized during ascent through the mantle in a thermal plume which originates in the lowermost mantle during formation of the Archean oceanic crust. Inclusion of such fractionated pods in the old subcontinental 'keel' of the Kaapvaal craton might constitute a potential PGE source, which could have been tapped by subsequent magmatic activity.

  13. Re-Os isotope and platinum group elements of a FOcal ZOne mantle source, Louisville Seamounts Chain, Pacific ocean

    NASA Astrophysics Data System (ADS)

    Tejada, Maria Luisa G.; Hanyu, Takeshi; Ishikawa, Akira; Senda, Ryoko; Suzuki, Katsuhiko; Fitton, Godfrey; Williams, Rebecca

    2015-02-01

    The Louisville Seamount Chain (LSC) is, besides the Hawaiian-Emperor Chain, one of the longest-lived hotspot traces. We report here the first Re-Os isotope and platinum group element (PGE) data for Canopus, Rigil, and Burton Guyots along the chain, which were drilled during IODP Expedition 330. The LSC basalts possess (187Os/188Os)i = 0.1245-0.1314 that are remarkably homogeneous and do not vary with age. A Re-Os isochron age of 64.9 ± 3.2 Ma was obtained for Burton seamount (the youngest of the three seamounts drilled), consistent with 40Ar-39Ar data. Isochron-derived initial 187Os/188Os ratio of 0.1272 ± 0.0008, together with data for olivines (0.1271-0.1275), are within the estimated primitive mantle values. This (187Os/188Os)i range is similar to those of Rarotonga (0.124-0.139) and Samoan shield (0.1276-0.1313) basalts and lower than those of Cook-Austral (0.136-0.155) and Hawaiian shield (0.1283-0.1578) basalts, suggesting little or no recycled component in the LSC mantle source. The PGE data of LSC basalts are distinct from those of oceanic lower crust. Variation in PGE patterns can be largely explained by different low degrees of melting under sulfide-saturated conditions of the same relatively fertile mantle source, consistent with their primitive mantle-like Os and primordial Ne isotope signatures. The PGE patterns and the low 187Os/188Os composition of LSC basalts contrast with those of Ontong Java Plateau (OJP) tholeiites. We conclude that the Re-Os isotope and PGE composition of LSC basalts reflect a relatively pure deep-sourced common mantle sampled by some ocean island basalts but is not discernible in the composition of OJP tholeiites.

  14. Laboratory partitioning of platinum-group elements (PGE) and gold with application to magmatic sulfide PGE deposits

    NASA Astrophysics Data System (ADS)

    Fleet, M. E.; Crocket, J. H.; Liu, Menghua; Stone, W. E.

    1999-06-01

    Apparent diversity in laboratory partitioning of platinum-group elements (PGE)-Au between (Fe,Ni)-sulfide liquid and S-saturated basaltic melt is resolved by recognizing the marked control exerted by variation in metal/S ratio of the sulfide liquid. Partition coefficients ( D) increase markedly for Os, Ir and Pd and somewhat for Pt with increase in S content. In addition, the partitioning is markedly dependent on concentration of PGE-Au in the sulfide fraction, for all precious metals in metal-rich sulfide, and for Ru, Pt and Pd in relatively S-rich sulfide. Reversal of partitioning of PGE-Au is presently demonstrated for experiments with metal-rich sulfide liquids. Erratic partitioning behaviour, with anomalously high D(PGE-Au) values, is minimised by degassing starting materials. Summary D(PGE-Au) values for metal-rich sulfide liquids and near-natural PGE-Au abundances are: Os(2.2), Ir(1.8), Ru(2.4), Pt(1.4), Pd(2.9), Au(0.9) (×10 3) for the CCO oxygen buffer and molar Ni/(Fe+Ni)=0.02, and Os(3.7), Ir(3.2), Ru(4.4), Pt(4.6), Pd(5.0), Au(3.0) (×10 3) for the IQF buffer and Ni/(Fe+Ni)=0.12. Thus, PGE-Au would not be extensively fractionated for equilibrium between sulfide and deep mantle melts. For more S-rich sulfide liquids (WM oxygen buffer) and 100-1000 ppm in the sulfide, D(PGE-Au) values are: Os(30), Ir(26), Ru(6.4), Pt(10), Pd(17) (×10 3) at Ni/(Fe+Ni)=0.36, and Os(10), Ir(51), Ru(3.5), Pt(13), Pd(25), Au (1.2) (×10 3) at Ni/(Fe+Ni)=0.66. The laboratory partitioning is notably differential within the PGE-Au group, with relatively high Ds for Ir and Pd and low Ds for Ru and Au. Although separation of an early-magmatic sulfide liquid would result in significant concentration of some PGE (e.g., Ir and Pd), sulfide liquid immiscibility alone would not account for the high abundance of PGE-Au in the reef deposits of the Bushveld and Stillwater Complexes.

  15. Platinum Group Elements (PGE) geochemistry of komatiites and boninites from Dharwar Craton, India: Implications for mantle melting processes

    NASA Astrophysics Data System (ADS)

    Saha, Abhishek; Manikyamba, C.; Santosh, M.; Ganguly, Sohini; Khelen, Arubam C.; Subramanyam, K. S. V.

    2015-06-01

    High MgO volcanic rocks having elevated concentrations of Ni and Cr are potential hosts for platinum group elements (PGE) owing to their primitive mantle origin and eruption at high temperatures. Though their higher PGE abundance is economically significant in mineral exploration studies, their lower concentrations are also valuable geochemical tools to evaluate petrogenetic processes. In this paper an attempt has been made to evaluate the PGE geochemistry of high MgO volcanic rocks from two greenstone belts of western and eastern Dharwar Craton and to discuss different mantle processes operative at diverse geodynamic settings during the Neoarchean time. The Bababudan greenstone belt of western and Gadwal greenstone belt of eastern Dharwar Cratons are dominantly composed of high MgO volcanic rocks which, based on distinct geochemical characteristics, have been identified as komatiites and boninites respectively. The Bababudan komatiites are essentially composed of olivine and clinopyroxene with rare plagioclase tending towards komatiitic basalts. The Gadwal boninites contain clinopyroxene, recrystallized hornblende with minor orthopyroxene, plagioclase and sulphide minerals. The Bababudan komatiites are Al-undepleted type (Al2O3/TiO2 = 23-59) with distinctly high MgO (27.4-35.8 wt.%), Ni (509-1066 ppm) and Cr (136-3036 ppm) contents. These rocks have low ΣPGE (9-42 ppb) contents with 0.2-2.4 ppb Iridium (Ir), 0.2-1.4 ppb Osmium (Os) and 0.4-4.4 ppb Ruthenium (Ru) among Iridium group PGE (IPGE); and 1.4-16.2 ppb Platinum (Pt), 2.8-19 ppb Palladium (Pd) and 0.2-9.8 ppb Rhodium (Rh) among Platinum group PGE (PPGE). The Gadwal boninites are high-Ca boninites with CaO/Al2O3 ratios varying between 0.8 and 1.0, with 12-24 wt.% MgO, 821-1168 ppm Ni and 2307-2765 ppm Cr. They show higher concentration of total PGE (82-207 ppb) with Pt concentration ranging from 13 to 19 ppb, Pd between 65 and 180 ppb and Rh in the range of 1.4-3 ppb compared to the Bababudan komatiites. Ir

  16. Evidence from meimechites and other low-degree mantle melts for redox controls on mantle-crust fractionation of platinum-group elements

    PubMed Central

    Mungall, James E.; Hanley, Jacob J.; Arndt, Nicholas T.; Debecdelievre, Anne

    2006-01-01

    Understanding of the geochemistry of the chalcophile elements [i.e., Os, Ir, Ru, Pt, Pd (platinum-group elements), and Au, Cu, Ni] has been informed for at least 20 years by the common assumption that when crust-forming partial melts are extracted from the upper mantle, sulfide liquid in the restite sequesters chalcophile elements until the extent of partial melting exceeds ≈25% and all of the sulfide has been dissolved in silicate melt [Hamlyn, P. R. & Keays, R. R. (1985) Geochim. Cosmochim. Acta 49, 1797–1811]. Here we document very high, unfractionated, chalcophile element concentrations in small-degree partial melts from the mantle that cannot be reconciled with the canonical residual sulfide assumption. We show that the observed high, unfractionated platinum-group element concentrations in small-degree partial melts can be attained if the melting takes place at moderately high oxygen fugacity, which will reduce the amount of sulfide due to the formation of sulfate and will also destabilize residual monosulfide solid solution by driving sulfide melts into the spinel-liquid divariant field. Magmas formed at high oxygen fugacity by small degrees of mantle melting can be important agents for the transfer of chalcophile elements from the upper mantle to the crust and may be progenitors of significant ore deposits of Pt, Pd, and Au. PMID:16908861

  17. Platinum-group element abundances and Re-Os isotopic systematics of the upper continental crust through time: Evidence from glacial diamictites

    NASA Astrophysics Data System (ADS)

    Chen, Kang; Walker, Richard J.; Rudnick, Roberta L.; Gao, Shan; Gaschnig, Richard M.; Puchtel, Igor S.; Tang, Ming; Hu, Zhao-Chu

    2016-10-01

    The fine-grained matrix of glacial diamictites, deposited periodically by continental ice sheets over much of Earth history, provides insights into the average composition and chemical evolution of the upper continental crust (UCC) (Gaschnig et al., 2016, and references therein). The concentrations of platinum-group elements (PGEs, including Os, Ir, Ru, Pt and Pd) and the geochemically related Re, as well as 187Re/188Os and 187Os/188Os ratios, are reported here for globally-distributed glacial diamictites that were deposited during the Mesoarchean, Paleoproterozoic, Neoproterozoic and Paleozoic eras. The medians and averages of PGE concentrations of these diamictite composites decrease from the Mesoarchean to the Neoproterozoic, mimicking decreases in the concentrations of first-row transition elements (Sc, V, Cr, Co and Ni). By contrast, Re concentrations are highly variable with no discernable trend, owing to its high solubility. Assuming these diamictites are representative of average UCC through time, the new data are fully consistent with the previous inference that the Archean UCC contained a greater proportion of mafic-ultramafic rocks relative to younger UCC. Linear regressions of PGEs versus Cr and Ni concentrations in all the diamictite composites from the four time periods are used to estimate the following concentrations of the PGEs in the present-day UCC: 0.059 ± 0.016 ng/g Os, 0.036 ± 0.008 ng/g Ir, 0.079 ± 0.026 ng/g Ru, 0.80 ± 0.22 ng/g Pt and 0.80 ± 0.26 ng/g Pd (2σ of 10,000 bootstrapping regression results). These PGE estimates are slightly higher than the estimates obtained from loess samples. We suggest this probably results from loess preferentially sampling younger UCC rocks that have lower PGE concentrations, or PGEs being fractionated during loess formation. A Re concentration of 0.25 ± 0.12 ng/g (2σ) is obtained from a regression of Re versus Mo. From this, time-integrated 187Re/188Os and 187Os/188Os ratios for the UCC are

  18. Ni, Cu, Au, and platinum-group element contents of sulphides associated with intraplate magmatism: A synthesis

    USGS Publications Warehouse

    Barnes, S.-J.; Zientek, M.L.; Severson, M.J.

    1997-01-01

    The tectonic setting of intraplate magmas, typically a plume intersecting a rift, is ideal for the development of Ni - Cu - platinum-group element-bearing sulphides. The plume transports metal-rich magmas close to the mantle - crust boundary. The interaction of the rift and plume permits rapid transport of the magma into the crust, thus ensuring that no sulphides are lost from the magma en route to the crust. The rift may contain sediments which could provide the sulphur necessary to bring about sulphide saturation in the magmas. The plume provides large volumes of mafic magma; thus any sulphides that form can collect metals from a large volume of magma and consequently the sulphides will be metal rich. The large volume of magma provides sufficient heat to release large quantities of S from the crust, thus providing sufficient S to form a large sulphide deposit. The composition of the sulphides varies on a number of scales: (i) there is a variation between geographic areas, in which sulphides from the Noril'sk - Talnakh area are the richest in metals and those from the Muskox intrusion are poorest in metals; (ii) there is a variation between textural types of sulphides, in which disseminated sulphides are generally richer in metals than the associated massive and matrix sulphides; and (iii) the massive and matrix sulphides show a much wider range of compositions than the disseminated sulphides, and on the basis of their Ni/Cu ratio the massive and matrix sulphides can be divided into Cu rich and Fe rich. The Cu-rich sulphides are also enriched in Pt, Pd, and Au; in contrast, the Fe-rich sulphides are enriched in Fe, Os, Ir, Ru, and Rh. Nickel concentrations are similar in both. Differences in the composition between the sulphides from different areas may be attributed to a combination of differences in composition of the silicate magma from which the sulphides segregated and differences in the ratio of silicate to sulphide liquid (R factors). The higher metal

  19. Positive anomaly in platinum group elements and the presence of shocked diamonds: Two question marks at the Younger Dryas

    NASA Astrophysics Data System (ADS)

    Claeys, P. F.; Schryvers, D.; Tian, H.; Goderis, S.

    2009-12-01

    Recently, a large size impact was proposed as the cause of the global changes taking place at the Younger Dryas (YD) some 12,9 kyr ago. Impact evidence was reported in a C-rich black layer of broad geographic distribution. The impact markers consist of a large anomaly in the concentration of platinum group elements (PGE) and the presence of nanodiamonds, in particular lonsdaleite, which hexagonal structure is believed to be of shock origin. The impact is proposed to have occurred on the North American continent. A crater large enough (> 150 km) to induce a mass extinction some ~12.9 ka ago, formed in a geologically well-known area, is unlikely to have escaped detection. Therefore, an alternative hypothesis is that a cometary projectile exploded fully within the atmosphere spreading PGE and shock formed diamonds, without any target rock contribution, all around the Northern hemisphere. So far, PGE measurements failed to reproduce the elevated (> ppb) concentrations reported previously at Younger Dryas sites containing the black layer. In Lommel (Belgium) where the first study detected up to 117 ppb Ir, the Ir concentration is below the detection limit of the method (NiS fire assay + ICP-MS) used (0.06 ppb). At all sites analyzed the PGE pattern is typical of that of the continental crust. In several craters (Popigai, Ries) or at the KT boundary nanodiamonds have been reported associated with shocked materials. Several types of carbon components occur in the black layer of the Lommel section such as i) flakes reaching up to 1 µm, ii) nano particles of cubic diamond, 1 to 10 nm in size and iii) larger carbon onion-ring structures, which core can act as a nanoscopic pressure cell leading to the formation of nanodiamond by self- compression. The Lommel nanodiamonds present in the Younger Dryas layer do resemble nanodiamonds found in carbon spherules of unknown origin previously reported in top soil from several localities in Belgium and Germany. The C stable isotopic

  20. Platinum-group element abundance and distribution in chromite deposits of the Acoje Block, Zambales Ophiolite Complex, Philippines

    USGS Publications Warehouse

    Bacuta, G.C.; Kay, R.W.; Gibbs, A.K.; Lipin, B.R.

    1990-01-01

    Platinum-group elements (PGE) occur in ore-grade concentration in some of the chromite deposits related to the ultramafic section of the Acoje Block of the Zambales Ophiolite Complex. The deposits are of three types: Type 1 - associated with cumulate peridotites at the base of the crust; Type 2 - in dunite pods from the top 1 km of mantle harzburgite; and Type 3 - like Type 2, but in deeper levels of the harzburgite. Most of the deposites have chromite compositions that are high in Cr with Cr/(Cr + Al) (expressed as chromium index, Cr#) > 0.6; high-Al (Cr# Pd, thought to be characteristic of PGE-barren deposits) and positive slope (Ir < Pd, characteristic of PGE-rich deposits). Iridium, Ru and Os commonly occur as micron-size laurite (sulfide) inclusions in unfractured chromite. Laurite and native Os are also found as inclusions in interstitial sulfides. Platinum and Pd occur as alloy inclusions (and possibly as solid solution) in interstitial Ni-Cu sulfides and as tellurobismuthides in serpentine and altered sulfides. Variability of PGE distribution may be explained by alteration, crystal fractionation or partial melting processes. Alteration and metamorphism were ruled out, because PGE contents do not correlate with degree of serpentinization or the abundance and type (hydroxyl versus non-hydroxyl) of silicate inclusions in chromite. Preliminary Os isotopic data do not support crustal contamination as a source of the PGEs in the Acoje deposits. The anomalous PGE concentrations in Type 1 high-Cr chromite deposits are attributed to two stages of enrichment: an early enrichment of their mantle source from previous melting events and a later stage of sulfide segregation accompanying chromite crystallization. High-Al chromite deposits which crystallized from basalts derived from relatively low degrees of melting owe their low PGE content to partitioning of PGEs in sulfides and alloys that remain in the mantle. High-Cr deposits crystallized from melts that were

  1. A Measurement of the Top Quark Mass in 1.96 TeV Proton-Antiproton Collisions Using a Novel Matrix Element Method

    SciTech Connect

    Freeman, John

    2007-01-01

    A measurement of the top quark mass in t$\\bar{t}$ → l + jets candidate events, obtained from p$\\bar{p}$ collisions at √s = 1.96 TeV at the Fermilab Tevatron using the CDF II detector, is presented. The measurement approach is that of a matrix element method. For each candidate event, a two dimensional likelihood is calculated in the top pole mass and a constant scale factor, 'JES', where JES multiplies the input particle jet momenta and is designed to account for the systematic uncertainty of the jet momentum reconstruction. As with all matrix element techniques, the method involves an integration using the Standard Model matrix element for t$\\bar{t}$ production and decay. However, the technique presented is unique in that the matrix element is modified to compensate for kinematic assumptions which are made to reduce computation time. Background events are dealt with through use of an event observable which distinguishes signal from background, as well as through a cut on the value of an event's maximum likelihood. Results are based on a 955 pb-1 data sample, using events with a high-pT lepton and exactly four high-energy jets, at least one of which is tagged as coming from a b quark; 149 events pass all the selection requirements. They find Mmeas = 169.8 ± 2.3(stat.) ± 1.4(syst.) GeV/c2.

  2. A measurement of the top quark mass in 1.96 TeV proton-antiproton collisions using a novel matrix element method

    SciTech Connect

    Freeman, John C

    2007-01-01

    A measurement of the top quark mass in t$\\bar{t}$ → l + jets candidate events, obtained from p$\\bar{p}$ collisions at √s = 1.96 TeV at the Fermilab Tevatron using the CDF II detector, is presented. The measurement approach is that of a matrix element method. For each candidate event, a two dimensional likelihood is calculated in the top pole mass and a constant scale factor, 'JES', where JES multiplies the input particle jet momenta and is designed to account for the systematic uncertainty of the jet momentum reconstruction. As with all matrix elements techniques, the method involves an integration using the Standard Model matrix element for tt production and decay. however, the technique presented is unique in that the matrix element is modified to compensate for kinematic assumptions which are made to reduce computation time. Background events are dealt with through use of an event observable which distinguishes signal from background, as well as through a cut on the value of an event's maximum likelihood. Results are based on a 955 pb-1 data sample, using events with a high-pT lepton and exactly four high-energy jets, at least one of which is tagged as coming from a b quark; 149 events pass all the selection requirements. They find Mmeas = 169.8 ± 2.3(stat.) ± 1.4(syst.) GeV/c2.

  3. Distribution of 23 elements in the kidney, liver and lungs of workers from a smeltery and refinery in North Sweden exposed to a number of elements and of a control group.

    PubMed

    Brune, D; Nordberg, G; Wester, P O

    1980-09-01

    The levels of antimony, arsenic, cadmium, caesium, chromium, cobalt, copper, gold, iron, lanthanum, lead, manganese, mercury, molybdenum, phosphorus, rubidium, scandium, selenium, silver, tellurium, tin, tungsten and zinc in the kidney, liver and lungs of autopsy specimens from exposed workers in North Sweden, as well as from a control group, have been assayed quantitatively. The workers had been exposed to several elements and their compounds, e.g. lead, mercury, arsenic and cadmium, for long periods in arsenic, lead or selenium plants and in a lead or copper smelter. The chemical analysis was by neutron activation analysis and atomic absorption spectrophotometry. Median levels of antimony, arsenic, cadmium, chromium cobalt, lanthanum, lead or selenium in kidney, liver or lungs in the exposed worker group were found to be about 2 to 16 times as great as the corresponding levels for the control group. Long biological half-life values were observed for these elements, especially in lung tissue.

  4. No Action Assurance Regarding EPA-Issued Step 2 Prevention of Significant Deterioraiton Permits and Related Title V Requirements Following Utility Air Regulatory Group v. Environmental Protection Agency

    EPA Pesticide Factsheets

    This document may be of assistance in applying the Title V air operating permit regulations. This document is part of the Title V Policy and Guidance Database available at www2.epa.gov/title-v-operating-permits/title-v-operating-permit-policy-and-guidance-document-index. Some documents in the database are a scanned or retyped version of a paper photocopy of the original. Although we have taken considerable effort to quality assure the documents, some may contain typographical errors. Contact the office that issued the document if you need a copy of the original.

  5. A divergent P element and its associated MITE, BuT5, generate chromosomal inversions and are widespread within the Drosophila repleta species group.

    PubMed

    Rius, Nuria; Delprat, Alejandra; Ruiz, Alfredo

    2013-01-01

    The transposon BuT5 caused two chromosomal inversions fixed in two Drosophila species of the repleta group, D. mojavensis and D. uniseta. BuT5 copies are approximately 1-kb long, lack any coding capacity, and do not resemble any other transposable element (TE). Because of its elusive features, BuT5 has remained unclassified to date. To fully characterize BuT5, we carried out bioinformatic similarity searches in available sequenced genomes, including 21 Drosophila species. Significant hits were only recovered for D. mojavensis genome, where 48 copies were retrieved, 22 of them approximately 1-kb long. Polymerase chain reaction (PCR) and dot blot analyses on 54 Drosophila species showed that BuT5 is homogeneous in size and has a widespread distribution within the repleta group. Thus, BuT5 can be considered as a miniature inverted-repeat TE. A detailed analysis of the BuT5 hits in D. mojavensis revealed three partial copies of a transposon with ends very similar to BuT5 and a P-element-like transposase-encoding region in between. A putatively autonomous copy of this P element was isolated by PCR from D. buzzatii. This copy is 3,386-bp long and possesses a seven-exon gene coding for an 822-aa transposase. Exon-intron boundaries were confirmed by reverse transcriptase-PCR experiments. A phylogenetic tree built with insect P superfamily transposases showed that the D. buzzatii P element belongs to an early diverging lineage within the P-element family. This divergent P element is likely the master transposon mobilizing BuT5. The BuT5/P element partnership probably dates back approximately 16 Ma and is the ultimate responsible for the generation of the two chromosomal inversions in the Drosophila repleta species group.

  6. A Divergent P Element and Its Associated MITE, BuT5, Generate Chromosomal Inversions and Are Widespread within the Drosophila repleta Species Group

    PubMed Central

    Rius, Nuria; Delprat, Alejandra; Ruiz, Alfredo

    2013-01-01

    The transposon BuT5 caused two chromosomal inversions fixed in two Drosophila species of the repleta group, D. mojavensis and D. uniseta. BuT5 copies are approximately 1-kb long, lack any coding capacity, and do not resemble any other transposable element (TE). Because of its elusive features, BuT5 has remained unclassified to date. To fully characterize BuT5, we carried out bioinformatic similarity searches in available sequenced genomes, including 21 Drosophila species. Significant hits were only recovered for D. mojavensis genome, where 48 copies were retrieved, 22 of them approximately 1-kb long. Polymerase chain reaction (PCR) and dot blot analyses on 54 Drosophila species showed that BuT5 is homogeneous in size and has a widespread distribution within the repleta group. Thus, BuT5 can be considered as a miniature inverted-repeat TE. A detailed analysis of the BuT5 hits in D. mojavensis revealed three partial copies of a transposon with ends very similar to BuT5 and a P-element-like transposase-encoding region in between. A putatively autonomous copy of this P element was isolated by PCR from D. buzzatii. This copy is 3,386-bp long and possesses a seven-exon gene coding for an 822-aa transposase. Exon–intron boundaries were confirmed by reverse transcriptase-PCR experiments. A phylogenetic tree built with insect P superfamily transposases showed that the D. buzzatii P element belongs to an early diverging lineage within the P-element family. This divergent P element is likely the master transposon mobilizing BuT5. The BuT5/P element partnership probably dates back approximately 16 Ma and is the ultimate responsible for the generation of the two chromosomal inversions in the Drosophila repleta species group. PMID:23682154

  7. Effect of replacing a hydroxyl group with a methyl group on arsenic (V) species adsorption on goethite (alpha-FeOOH).

    PubMed

    Zhang, J S; Stanforth, R S; Pehkonen, S O

    2007-02-01

    Arsenate and methylated arsenicals, such as dimethylarsinate (DMA) and monomethylarsonate (MMA), are being found with increasing frequency in natural water systems. The mobility and bioavailability of these arsenic species in the environment are strongly influenced by their interactions with mineral surface, especially iron and aluminum oxides. Goethite (alpha-FeOOH), one of the most abundant ferric (hydr)oxides in natural systems, has a high retention capacity for arsenic species. Unfortunately, the sorption mechanism for the species is not completely understood, which limits our ability to model their behavior in natural systems. The purpose of this study is to investigate the effect of replacing a hydroxyl group with a methyl group on the adsorption behaviors of arsenic (V) species using adsorption edges, the influence of the background electrolyte on arsenic adsorption, and their effect on the zeta potential of goethite. The affinity of the three species to the goethite surface decreases in the order of AsO4=MMA>DMA. The uptake of DMA and MMA is independent of the concentration of background electrolyte, indicating that both species form inner-sphere complexes on the goethite surface and the most charge of adsorbed DMA and MMA locates at the surface plane. Arsenate uptake increases with increasing concentrations of background electrolyte at pH above 4, possibly due to that the charge of adsorbed arsenate is distributed between the surface plane and another electrostatic plane. DMA and lower concentrations of MMA have small effect on the zeta potential, whereas the zeta potential of goethite decreases in the presence of arsenate. The small effect on zeta potential of DMA or MMA adsorption suggests that the sorption sites for the anions is not important in controlling the surface charge. This observation is inconsistent with most adsorption models that postulate a singly coordinated hydroxyls contributing to both the adsorption and the surface charge, but

  8. A monochromator for tuning the photon energy range 600 eV and 6000 eV with a single dispersing optical element (Conference Presentation)

    NASA Astrophysics Data System (ADS)

    Jark, Werner H.

    2016-09-01

    Recently it was found that reflection gratings of standard quality, which can be used at lower energy soft X-rays with photon energies of the order of 300 eV, diffract also efficiently X-rays with photon energies of the order of 5 keV, when these gratings are operated at grazing angle of incidence in the extreme off-plane configuration [1]. Consequently a grating employed in the extreme off-plane configuration has the capability to provide monochromatic radiation in the photon energy range from below 1 keV to far above 2 keV, where one usually switches for the same purpose between the diffraction at surface structures and the diffraction in bulk structures. Such an operation scheme requires rather complex mechanical structures. The present study will show that the tuning of diffraction gratings in the conical diffraction configuration can cover the indicated and even more extended tuning ranges employing a rather simple mechanical structure. Infact such a grating can be mounted together with a plane mirror in a pseudo channel-cut crystal monochromator configuration, i.e. with almost parallel surfaces and with fixed gap between them. The photon energy is then tuned simply by varying the angle of grazing incidence onto the pair of optics. Like in a double crystal monochromator scheme the monochromatic beam will exit from the configuration parallel to the incident beam with in most cases negligibly varying displacement in the plane of incidence. The optical performance data will be discussed depending on the properties of some state-of-the-art synchrotron radiation sources. [1] W. Jark and D. Eichert, Opt. Express 23, 22753 (2015).

  9. Effects of Oxygen Element and Oxygen-Containing Functional Groups on Surface Wettability of Coal Dust with Various Metamorphic Degrees Based on XPS Experiment

    PubMed Central

    Zhou, Gang; Xu, Cuicui; Cheng, Weimin; Zhang, Qi; Nie, Wen

    2015-01-01

    To investigate the difference of surface oxygen element and oxygen-containing functional groups among coal dusts with different metamorphic degrees and their influence on surface wettability, a series of X-ray photoelectron spectroscopy experiments on 6 coal samples are carried out. The result demonstrates that the O/C ratio of coal surface shows an overall increasing trend compared with the result of its elements analysis. As the metamorphic degree increases, the O/C ratio on the surface gradually declines and the hydrophilic groups tend to fall off from coal surface. It could be found that different coals show different surface distributions of carboxyl and hydroxyl which are considered as the greatest promoter to the wettability of coal surface. With the change of metamorphic degree, the distribution of ether group is irregular while the carbonyl distribution keeps stable. In general, as the metamorphic degree goes higher, the content of oxygen-containing polar group tends to reduce. According to the measurement results, the contact angle is negatively related to the content of oxygen element, surface oxygen, and polar groups. In addition, compared with surface oxygen content, the content of oxygen-containing polar group serves as a more reasonable indicator of coal dust wettability. PMID:26257980

  10. Sequence analysis of a group of low molecular-weight plasmids carrying multiple IS903 elements flanking a kanamycin resistance aph gene in Salmonella enterica serovars

    Technology Transfer Automated Retrieval System (TEKTRAN)

    A group of low molecular-weight ColE1-like plasmids carrying the aph sequence type aph(ii), from three different Salmonella serovars were sequenced. These plasmids carry 2 or more copies of IS903 elements, with up to 21 bp sequence differences to one another, two of which flank the aph gene. This g...

  11. Differential occurrence of chromosome inversion polymorphisms among Muller's elements in three species of the tripunctata group of Drosophila, including a species with fast chromosomal evolution.

    PubMed

    Brianti, Mitsue T; Ananina, Galina; Klaczko, Louis B

    2013-01-01

    Detailed chromosome maps with reliable homologies among chromosomes of different species are the first step to study the evolution of the genetic architecture in any set of species. Here, we present detailed photo maps of the polytene chromosomes of three closely related species of the tripunctata group (subgenus Drosophila): Drosophila mediopunctata, D. roehrae, and D. unipunctata. We identified Muller's elements in each species, using FISH, establishing reliable chromosome homologies among species and D. melanogaster. The simultaneous analysis of chromosome inversions revealed a distribution pattern for the inversion polymorphisms among Muller's elements in the three species. Element E is the most polymorphic, with many inversions in each species. Element C follows; while the least polymorphic elements are B and D. While interesting, it remains to be determined how general this pattern is among species of the tripunctata group. Despite previous studies showing that D. mediopunctata and D. unipunctata are phylogenetically closer to each other than to D. roehrae, D. unipunctata shows rare karyotypic changes. It has two chromosome fusions: an additional heterochromatic chromosome pair and a pericentric inversion in the X chromosome. This especial conformation suggests a fast chromosomal evolution that deserves further study.

  12. Behavior of iron-group elements, oxybarometry, and genesis of unique chromite deposits in the Kempirsai massif

    NASA Astrophysics Data System (ADS)

    Chashchukhin, I. S.; Votyakov, S. L.

    2009-04-01

    Ultramafic rocks and high-Cr chromite ore from the Almaz-Zhemchuzhina deposit, the largest in the Main ore field of the Kempirsai massif, have been studied. The detailed mineralogical and geochemical examination of deep structure test and exploratory boreholes allowed us to establish the rough stratification of ultramafic rocks and to demonstrate the position of unique chromite deposits in the generalized vertical section of the southeastern Kempirsai massif. From top to bottom, a barren harzburgite-lherzolite series gives way to an ore-bearing dunite-harzburgite complex with the largest chromite deposits, including the unique Almaz-Zhemchuzhina deposit, in its upper portion and then to pyroxene-free dunite densely impregnated with chromite in the upper part and containing sparsely disseminated chromite at its base. The lower unit is composed of a barren lherzolite-harzburgite series transformed into blastomylonites near the contact with dunite, suggesting a tectonically doubled section in the southeastern part of the massif. The synore asymmetric geochemical zoning developed in the course of formation of chromite deposits as a result of removal of oreforming iron-group elements from the underlying and wall ultramafic rocks into the overlying rocks. Host rocks with disturbed initial proportions of Cr, Fe, Ni, and Mn, together with orebodies, made up ore-bearing zones no less than 1 km in thickness and subdivided into supra-, inter-, and subore subzones. The subore and wall rocks are characterized by partial loss (wt %) of Cr2O3(0.1), NiO (0.04), FeOtot(0.5), and MnO (0.02) and their removal into the interore and supraore (0.03 NiO) subzones. Thus, the subore ultramafic rocks served as a source of ore-forming components, while the interore zone with orebodies occurring therein served as a zone of discharge of these components. Using Mössbauer spectroscopy, the crystal chemistry of iron ions was studied in a representative selection of Cr-spinel samples from rocks

  13. The role of group 14 element hydrides in the activation of C-H bonds in cyclic olefins.

    PubMed

    Summerscales, Owen T; Caputo, Christine A; Knapp, Caroline E; Fettinger, James C; Power, Philip P

    2012-09-05

    Formally, triple-bonded dimetallynes ArEEAr [E = Ge (1), Sn (2); Ar = C(6)H(3)-2,6-(C(6)H(3)-2,6-(i)Pr(2))(2)] have been previously shown to activate aliphatic, allylic C-H bonds in cyclic olefins, cyclopentadiene (CpH), cyclopentene (c-C(5)H(8)) and 1,4-cyclohexadiene, with intriguing selectivity. In the case of the five-membered carbocycles, cyclopentadienyl species ArECp [E = Ge (3), Sn (4)] are formed. In this study, we examine the mechanisms for activation of CpH and c-C(5)H(8) using experimental methods and describe a new product found from the reaction between 1 and c-C(5)H(8), an asymmetrically substituted digermene ArGe(H)Ge(c-C(5)H(9))Ar (5), crystallized in 46% yield. This compound contains a hydrogenated cyclopentyl moiety and is found to be produced in a 3:2 ratio with 3, explaining the fate of the liberated H atoms following triple C-H activation. We show that when these C-H activation reactions are carried out in the presence of tert-butyl ethylene (excess), compounds {ArE(CH(2)CH(2)tBu)}(2) [E = Ge(8), Sn(9)] are obtained in addition to ArECp; in the case of CpH, the neohexyl complexes replace the production of H(2) gas, and for c-C(5)H(8) they displace cyclopentyl product 5 and account for all the hydrogen removed in the dehydroaromatization reactions. To confirm the source of 8 and 9, it was demonstrated that these molecules are formed cleanly between the reaction of (ArEH)(2) [E = Ge(6), Sn(7)] and tert-butyl ethylene, new examples of noncatalyzed hydro-germylation and -stannylation. Therefore, the presence of transient hydrides of the type 6 and 7 can be surmised to be reactive intermediates in the production of 3 and 4, along with H(2), from 1 and 2 and CpH (respectively), or the formation of 3 and 5 from 1. The reaction of 6 or 7 with CpH gave 3 or 4, respectively, with concomitant H(2) evolution, demonstrating the basic nature of these low-valent group 14 element hydrides and their key role in the 'cascade' of C-H activation steps

  14. FB-NOF is a non-autonomous transposable element, expressed in Drosophila melanogaster and present only in the melanogaster group.

    PubMed

    Badal, Martí; Xamena, Noel; Cabré, Oriol

    2013-09-10

    Most foldback elements are defective due to the lack of coding sequences but some are associated with coding sequences and may represent the entire element. This is the case of the NOF sequences found in the FB of Drosophila melanogaster, formerly considered as an autonomous TE and currently proposed as part of the so-called FB-NOF element, the transposon that would be complete and fully functional. NOF is always associated with FB and never seen apart from the FB inverted repeats (IR). This is the reason why the FB-NOF composite element can be considered the complete element. At least one of its ORFs encodes a protein that has always been considered its transposase, but no detailed studies have been carried out to verify this. In this work we test the hypothesis that FB-NOF is an active transposon nowadays. We search for its expression product, obtaining its cDNA, and propose the ORF and the sequence of its potential protein. We found that the NOF protein is not a transposase as it lacks any of the motifs of known transposases and also shows structural homology with hydrolases, therefore FB-NOF cannot belong to the superfamily MuDR/foldback, as up to now it has been classified, and can be considered as a non-autonomous transposable element. The alignment with the published genomes of 12 Drosophila species shows that NOF presence is restricted only to the 6 Drosophila species belonging to the melanogaster group.

  15. Efficacy of cefuroxime axetil suspension compared with that of penicillin V suspension in children with group A streptococcal pharyngitis.

    PubMed Central

    Gooch, W M; McLinn, S E; Aronovitz, G H; Pichichero, M E; Kumar, A; Kaplan, E L; Ossi, M J

    1993-01-01

    The bacteriological and clinical efficacies of cefuroxime axetil suspension (20 mg/kg of body weight per day in two divided doses) were compared with those of penicillin V suspension (50 mg/kg/day in three divided doses) in a multicenter, randomized, evaluator-blinded study. Children aged 2 to 13 years with clinical signs and symptoms of acute pharyngitis and a positive throat culture for group A beta-hemolytic streptococci (GABHS) were eligible. Patients were assessed and samples from the throat for culture were obtained at the time of diagnosis, 3 to 7 days after the initiation of treatment, and 4 to 8 days and 19 to 25 days after the completion of 10 days of therapy. Of the 385 evaluable patients, GABHS were eradicated from 244 of 259 (94.2%) cefuroxime-treated patients and 106 of 126 (84.1%) penicillin-treated patients (P = 0.001). Complete resolution of the signs and symptoms present at the time of diagnosis was achieved in 238 of 259 (91.9%) cefuroxime-treated patients and 102 of 126 (81.0%) penicillin-treated patients (P = 0.001). Potential drug-related adverse events were reported in 7.0 and 3.2% of the cefuroxime- and penicillin-treated patients, respectively (P = 0.078). In the present study, cefuroxime axetil suspension given twice daily resulted in significantly greater bacteriological and clinical efficacies than those of penicillin V suspension given three times daily to pediatric patients with acute pharyngitis and a positive throat culture for GABHS. PMID:8452344

  16. Isolation of a novel IS3 group insertion element and construction of an integration vector for Lactobacillus spp.

    PubMed Central

    Walker, D C; Klaenhammer, T R

    1994-01-01

    An insertion sequence (IS) element from Lactobacillus johnsonii was isolated, characterized, and exploited to construct an IS-based integration vector. L. johnsonii NCK61, a high-frequency conjugal donor of bacteriocin production (Laf+) and immunity (Lafr), was transformed to erythromycin resistance (Emr) with the shuttle vector pSA3. The NCK61 conjugative functions were used to mobilize pSA3 into a Laf- Lafs EMs recipient. DNA from the Emr transconjugants transformed into Escherichia coli MC1061 yielded a resolution plasmid with the same size as that of pSA3 with a 1.5-kb insertion. The gram-positive replication region of the resolution plasmid was removed to generate a pSA3-based suicide vector (pTRK327) bearing the 1.5-kb insert of Lactobacillus origin. Plasmid pTRK327 inserted randomly into the chromosomes of both Lactobacillus gasseri ATCC 33323 and VPI 11759. No homology was detected between plasmid and total host DNAs, suggesting a Rec-independent insertion. The DNA sequence of the 1.5-kb region revealed the characteristics of an IS element (designated IS1223): a length of 1,492 bp; flanking, 25-bp, imperfect inverted repeats; and two overlapping open reading frames (ORFs). Sequence comparisons revealed 71.1% similarity, including 35.7% identity, between the deduced ORFB protein of the E. coli IS element IS150 and the putative ORFB protein encoded by the Lactobacillus IS element. A putative frameshift site was detected between the overlapping ORFs of the Lactobacillus IS element. It is proposed that, similar to IS150, IS1223 produces an active transposase via translational frameshifting between two tandem, overlapping ORFs. Images PMID:8071209

  17. 20 CFR 655.1115 - Element V-What does “no strike/lockout or layoff” mean?

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... Facility Meet to Employ H-1C Nonimmigrant Workers as Registered Nurses? § 655.1115 Element V—What does “no... not lay off a registered nurse employed by the facility within the period beginning 90 days before and... intended or designated to influence an election for a bargaining representative for registered nurses...

  18. A Strategy for Preservice Teachers to Integrate Cultural Elements within Planning and Instruction: Cultural L.I.V.E.S.

    ERIC Educational Resources Information Center

    Salsbury, Denise E.

    2008-01-01

    The large percentages of teachers in the United States are white, middle class people who may not understand or identify their own cultural connections within the American culture, let alone elaborate their own ancestral cultural elements. Educators are expected to teach a diverse student population, and preservice teachers should be prepared to…

  19. 20 CFR 655.1115 - Element V-What does “no strike/lockout or layoff” mean?

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... Facility Meet to Employ H-1C Nonimmigrant Workers as Registered Nurses? § 655.1115 Element V—What does “no... not lay off a registered nurse employed by the facility within the period beginning 90 days before and... intended or designated to influence an election for a bargaining representative for registered nurses...

  20. 20 CFR 655.1115 - Element V-What does “no strike/lockout or layoff” mean?

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... Facility Meet to Employ H-1C Nonimmigrant Workers as Registered Nurses? § 655.1115 Element V—What does “no... not lay off a registered nurse employed by the facility within the period beginning 90 days before and... intended or designated to influence an election for a bargaining representative for registered nurses...

  1. 20 CFR 655.1115 - Element V-What does “no strike/lockout or layoff” mean?

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... Facility Meet to Employ H-1C Nonimmigrant Workers as Registered Nurses? § 655.1115 Element V—What does “no... not lay off a registered nurse employed by the facility within the period beginning 90 days before and... intended or designated to influence an election for a bargaining representative for registered nurses...

  2. A meiotic drive element in the maize pathogen Fusarium verticillioides is located within a 102-kb region of chromosome V

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Fusarium verticillioides is an agriculturally important fungus because of its association with maize and its propensity to contaminate grain with toxic compounds. Some isolates of the fungus harbor a meiotic drive element known as Spore killer (SkK) that causes nearly all surviving meiotic progeny f...

  3. Rhenium-osmium isotope and platinum-group elements in the Xinjie layered intrusion, SW China: Implications for source mantle composition, mantle evolution, PGE fractionation and mineralization

    NASA Astrophysics Data System (ADS)

    Zhong, Hong; Qi, Liang; Hu, Rui-Zhong; Zhou, Mei-Fu; Gou, Ti-Zhong; Zhu, Wei-Guang; Liu, Bing-Guang; Chu, Zhu-Yin

    2011-03-01

    The Xinjie mafic-ultramafic layered intrusion in the Emeishan large igneous province (ELIP) hosts Cu-Ni-platinum group element (PGE) sulfide ore layers within the lower part and Fe-Ti-V oxide-bearing horizons within the middle part. The major magmatic Cu-Ni-PGE sulfide ores and spatially associated cumulate rocks are examined for their PGE contents and Re-Os isotopic systematics. The samples yielded a Re-Os isochron with an age of 262 ± 27 Ma and an initial 187Os/ 188Os of 0.12460 ± 0.00011 ( γOs( t) = -0.5 ± 0.1). The age is in good agreement with the previously reported U-Pb zircon age, indicating that the Re-Os system remained closed for most samples since the intrusion emplacement. They have near-chondritic γOs( t) values ranging from -0.7 to -0.2, similar to those of the Lijiang picrites and Song Da komatiites. Exceptionally, two samples from the roof zone and one from upper sequence exhibit radiogenic γOs( t) values (+0.6 to +8.6), showing minor contamination by the overlying Emeishan basalts. The PGE-rich ores contain relatively high PGE and small amounts of sulfides (generally less than 2%) and the abundance of Cu and PGE correlate well with S, implying that the distribution of these elements is controlled by the segregation and accumulation of a sulfide liquid. Some ore samples are poor in S (mostly <800 ppm), which may due to late-stage S loss caused by the dissolution of FeS from pre-existing sulfides through their interaction with sulfide-unsaturated flowing magma. The combined study shows that the Xinjie intrusion may be derived from ferropicritic magmas. The sharp reversals in Mg#, Cr/FeO T and Cr/TiO 2 ratios immediately below Units 2-4, together with high Cu/Zr ratios decreasing from each PGE ore layer within these cyclic units, are consistent with multiple magma replenishment episodes. The sulfides in the cumulate rocks show little evidence of PGE depletion with height and thus appear to have segregated from successive inputs of fertile magma

  4. Theoretical predictions of properties and volatility of chlorides and oxychlorides of group-4 elements. I. Electronic structures and properties of MCl₄ and MOCl₂ (M = Ti, Zr, Hf, and Rf).

    PubMed

    Pershina, V; Borschevsky, A; Iliaš, M

    2014-08-14

    Relativistic, infinite order exact two-component, density functional theory electronic structure calculations were performed for MCl4 and MOCl2 of group-4 elements Ti, Zr, Hf, and element 104, Rf, with the aim to predict their behaviour in gas-phase chromatography experiments. RfCl4 and RfOCl2 were shown to be less stable than their lighter homologs in the group, tetrachlorides and oxychlorides of Zr and Hf, respectively. The oxychlorides turned out to be stable as a bent structure, though the stabilization energy with respect to the flat one (C(2v)) is very small. The trend in the formation of the tetrachlorides from the oxychlorides in group 4 is shown to be Zr < Hf < Rf, while the one in the formation of the oxychlorides from the chlorides is opposite. All the calculated properties are used to estimate adsorption energy of these species on various surfaces in order to interpret results of gas-phase chromatography experiments, as is shown in Paper II.

  5. Theoretical predictions of properties and volatility of chlorides and oxychlorides of group-4 elements. I. Electronic structures and properties of MCl{sub 4} and MOCl{sub 2} (M = Ti, Zr, Hf, and Rf)

    SciTech Connect

    Pershina, V.; Borschevsky, A.; Iliaš, M.

    2014-08-14

    Relativistic, infinite order exact two-component, density functional theory electronic structure calculations were performed for MCl{sub 4} and MOCl{sub 2} of group-4 elements Ti, Zr, Hf, and element 104, Rf, with the aim to predict their behaviour in gas-phase chromatography experiments. RfCl{sub 4} and RfOCl{sub 2} were shown to be less stable than their lighter homologs in the group, tetrachlorides and oxychlorides of Zr and Hf, respectively. The oxychlorides turned out to be stable as a bent structure, though the stabilization energy with respect to the flat one (C{sub 2v}) is very small. The trend in the formation of the tetrachlorides from the oxychlorides in group 4 is shown to be Zr < Hf < Rf, while the one in the formation of the oxychlorides from the chlorides is opposite. All the calculated properties are used to estimate adsorption energy of these species on various surfaces in order to interpret results of gas-phase chromatography experiments, as is shown in Paper II.

  6. Group V Secretory Phospholipase A2 Is Involved in Tubular Integrity and Sodium Handling in the Kidney

    PubMed Central

    Moraes-Santos, Felipe; Landgraf, Sharon Schilling; Silva, Leandro Souza; Sirtoli, Gabriela Modenesi; Zamith-Miranda, Daniel; Takiya, Christina Maeda; Pinheiro, Ana Acacia Sá; Diaz, Bruno Lourenço; Caruso-Neves, Celso

    2016-01-01

    Group V (GV) phospholipase A2 (PLA2) is a member of the family of secreted PLA2 (sPLA2) enzymes. This enzyme has been identified in several organs, including the kidney. However, the physiologic role of GV sPLA2 in the maintenance of renal function remains unclear. We used mice lacking the gene encoding GV sPLA2 (Pla2g5−/−) and wild-type breeding pairs in the experiments. Mice were individually housed in metabolic cages and 48-h urine was collected for biochemical assays. Kidney samples were evaluated for glomerular morphology, renal fibrosis, and expression/activity of the (Na+ + K+)-ATPase α1 subunit. We observed that plasma creatinine levels were increased in Pla2g5−/− mice following by a decrease in creatinine clearance. The levels of urinary protein were higher in Pla2g5−/− mice than in the control group. Markers of tubular integrity and function such as γ-glutamyl transpeptidase, lactate dehydrogenase, and sodium excretion fraction (FENa+) were also increased in Pla2g5−/− mice. The increased FENa+ observed in Pla2g5−/− mice was correlated to alterations in cortical (Na+ + K+) ATPase activity/ expression. In addition, the kidney from Pla2g5−/− mice showed accumulation of matrix in corticomedullary glomeruli and tubulointerstitial fibrosis. These data suggest GV sPLA2 is involved in the maintenance of tubular cell function and integrity, promoting sodium retention through increased cortical (Na+ + K+)-ATPase expression and activity. PMID:26820468

  7. Increase in platinum group elements in Mexico City as revealed from growth rings of Taxodium mucronatum ten.

    PubMed

    Morton-Bermea, Ofelia; Beramendi-Orosco, Laura; Martínez-Reyes, Ángeles; Hernández-Álvarez, Elizabeth; González-Hernández, Galia

    2016-02-01

    Tree rings may be used as indicators of contamination events providing information on the chronology and the elemental composition of the contamination. In this framework, we report PGEs enrichment in growth rings of Taxodium mucronatum ten for trees growing in the central area of Mexico City as compared to trees growing in a non-urban environment. Concentrations of PGE were determined by ICP-MS analysis on microwave-digested tree rings. The element found in higher concentrations was Pd (1.13-87.98 μg kg(-1)), followed by Rh (0.28-36.81 μg kg(-1)) and Pt (0.106-7.21 μg kg(-1)). The concentration trends of PGEs in the tree-ring sequences from the urban area presented significant correlation values when comparing between trees (r between 0.618 and 0.98, P < 0.025) and between elements within individual trees (r between 0.76 and 0.994, P < 0.01). Furthermore, a clear increase was observed for rings after 1997, with enrichment of up to 60 times the mean concentration found for the sequence from the non-urban area and up to 40 times the mean concentration for the pre-1991 period in the urban trees. These results also demonstrate the feasibility of applying T. mucronatum ten to be used as a bioindicator of the increase in PGE in urban environments.

  8. Three groups of transposable elements with contrasting copy number dynamics and host responses in the maize (Zea mays ssp. mays) genome.

    PubMed

    Diez, Concepcion M; Meca, Esteban; Tenaillon, Maud I; Gaut, Brandon S

    2014-04-01

    Most angiosperm nuclear DNA is repetitive and derived from silenced transposable elements (TEs). TE silencing requires substantial resources from the plant host, including the production of small interfering RNAs (siRNAs). Thus, the interaction between TEs and siRNAs is a critical aspect of both the function and the evolution of plant genomes. Yet the co-evolutionary dynamics between these two entities remain poorly characterized. Here we studied the organization of TEs within the maize (Zea mays ssp mays) genome, documenting that TEs fall within three groups based on the class and copy numbers. These groups included DNA elements, low copy RNA elements and higher copy RNA elements. The three groups varied statistically in characteristics that included length, location, age, siRNA expression and 24:22 nucleotide (nt) siRNA targeting ratios. In addition, the low copy retroelements encompassed a set of TEs that had previously been shown to decrease expression within a 24 nt siRNA biogenesis mutant (mop1). To investigate the evolutionary dynamics of the three groups, we estimated their abundance in two landraces, one with a genome similar in size to that of the maize reference and the other with a 30% larger genome. For all three accessions, we assessed TE abundance as well as 22 nt and 24 nt siRNA content within leaves. The high copy number retroelements are under targeted similarly by siRNAs among accessions, appear to be born of a rapid bust of activity, and may be currently transpositionally dead or limited. In contrast, the lower copy number group of retrolements are targeted more dynamically and have had a long and ongoing history of transposition in the maize genome.

  9. Cathodoluminescence zoning and minor elements in forsterites from the Murchison (C2) and Allende (C3V) carbonaceous chondrites

    NASA Technical Reports Server (NTRS)

    Steele, I. M.; Smith, J. V.; Skirius, C.

    1985-01-01

    Cathodoluminescence has been applied to look for textural features of olivine in carbonaceous meteorites relevant to the unresolved dispute over the origin of the olivine, whether from a vapor or a liquid. Cathodoluminescence photographs of forsterite grains in Murchison (C2) and Allende (C3) meteorites presented here reveal a blue core with planar boundaries to a red or dark rim. High-precision electron microprobe analyses have been performed which reveal unusually large amounts of the 'minor' elements Al, Ti, and Ca in the blue cores of these forsterites, suggesting formation by crystallization at high temperatures from a source rich in these metals. Following conclusions drawn from previous analyses of olivine in meteorites, it is argued that the minor element signature should be able to characterize olivines in micrometeorites and in deep-sea particles.

  10. Understanding the On-Off Switching Mechanism in Cationic Tetravalent Group-V-Based Fluoride Molecular Sensors Using Orbital Analysis.

    PubMed

    Usui, Kosuke; Ando, Mikinori; Yokogawa, Daisuke; Irle, Stephan

    2015-12-24

    The precise control of on-off switching is essential to the design of ideal molecular sensors. To understand the switching mechanism theoretically, we selected as representative example a 9-anthryltriphenylstibonium cation, which was reported as a fluoride ion sensor. In this molecule, the first excited singlet state exhibits two minimum geometries, where one of them is emissive and the other one dark. The excited state at the geometry with bright emission is of π-π* character, whereas it is of π-σ* character at the "dark" geometry. Geometry changes in the excited state were identified by geometry optimization and partial potential energy surface (PES) mapping. We also studied Group V homologues of this molecule. A barrierless relaxation pathway after vertical excitation to the "dark" geometry was found for the Sb-containing compound on the excited-states PES, whereas barriers appear in the case of P and As. Molecular orbital analysis suggests that the σ* orbital of the antimony compound is stabilized along such relaxation and that the excited state changes its nature correspondingly. Our results indicate that the size of the central atom is crucial for the design of fluoride sensors with this ligand framework.

  11. The origin and evolution of the odd-Z iron-peak elements Sc, V, Mn, and Co in the Milky Way stellar disk

    NASA Astrophysics Data System (ADS)

    Battistini, Chiara; Bensby, Thomas

    2015-05-01

    Context. Elements heavier than Li are produced in the interiors of stars. However, for many elements the exact production sites and the timescales on which they are dispersed into the interstellar medium are unknown. Having a clear picture on the origins of the elements is important for our ability to trace and understand the formation and chemical evolution of the Milky Way and its stellar populations. Aims: The aim of this study is to investigate the origin and evolution of Sc, V, Mn, and Co for a homogeneous and statistically significant sample of stars probing the different populations of the Milky Way, in particular the thin and thick disks. Methods: Using high-resolution spectra obtained with the MIKE, FEROS, SOFIN, FIES, UVES, and HARPS spectrographs, we determine Sc, V, Mn, and Co abundances for a large sample of F and G dwarfs in the solar neighborhood. The method is based on spectral synthesis and using one-dimensional, plane-parallel, local thermodynamic equilibrium (LTE) model stellar atmospheres calculated with the MARCS 2012 code. The non-LTE (NLTE) corrections from the literature were applied to Mn and Co. Results: We find that the abundance trends derived for Sc (594 stars), V (466 stars), and Co (567 stars) are very similar to what has been observed for the α-elements in the thin and thick disks. On the contrary, Mn (569 stars) is generally underabundant relative to the Sun (i.e., [ Mn/Fe ] < 0) for [ Fe/H ] < 0. In addition, for Mn, when NLTE corrections are applied, the trend changes and is almost flat over the entire metallicity range of the stars in our sample (-2 ≲ [ Fe/H ] ≲ + 0.4). The [Sc/Fe]-[Fe/H] abundance trends show a small separation between the thin and thick disks, while for V and Co they completely overlap. For Mn there is a small difference in [Mn/Fe], but only when NLTE corrections are used. Comparisons with Ti as a reference element show flat trends for all the elements except for Mn that show well separated [Mn

  12. Determination of platinum group elements by inductively coupled plasma-mass spectrometry combined with nickel sulfide fire assay and tellurium coprecipitation

    NASA Astrophysics Data System (ADS)

    Sun, Yali; Guan, Xiyun; Du, Andao

    1998-09-01

    A method was developed for the determination of trace platinum group elements (PGEs) by nickel sulfide fire assay inductively coupled plasma-mass spectrometry (ICP-MS). With isotope dilution, the improved technique gives precise Os content data. Through the purification of the reagent nickel oxide, reagent blank was greatly reduced. Results obtained for the standard reference materials (SRM) GPt-1-GPt-7(GBW 07288-07294, China), DZ Σ-2 (GBW 07102, China) and Guilin Cu-Ni Ore are in good agreement with the recommended values for platinum group elements. The detection limits ranged from 0.01 to 0.39 ng/g. The relative standard deviations for Ru, Rh, Pd and Ir were less than 5%, for Os less than 1%, and Pt less than 8% for SRM GPt-6.

  13. Spin-orbit effects, VSEPR theory, and the electronic structures of heavy and superheavy group IVA hydrides and group VIIIA tetrafluorides. A partial role reversal for elements 114 and 118

    SciTech Connect

    Nash, C.S.; Bursten, B.E.

    1999-01-21

    Relativistic effective core potentials and spin-orbit operators are used in relativistic configuration interaction calculations to explore the effects of spin-orbit coupling on the electronic structures of atoms and molecules of elements 114 and 118. The monohydrides of group IVA and the tetrafluorides of group VIIIA are examined in order to provide examples of trends within families among the various periods. The spin-orbit effect is found to play a dominant role in the determination of atomic and molecular properties. Several nonintuitive consequences of spin-orbit coupling are presented, including the depiction of element 114 as a closed-shell noble atom and the suggestion that the VSEPR theory in inadequate to describe the geometry of the rare gas tetrafluoride, (118)F{sub 4}.

  14. First measurement of the ratio B(t --> Wb)/B(t --> Wq) and associated limit on the Cabibbo-Kobayashi-Maskawa element /V(tb)/.

    PubMed

    Affolder, T; Akimoto, H; Akopian, A; Albrow, M G; Amaral, P; Amendolia, S R; Amidei, D; Anikeev, K; Antos, J; Apollinari, G; Arisawa, T; Asakawa, T; Ashmanskas, W; Azfar, F; Azzi-Bacchetta, P; Bacchetta, N; Bailey, M W; Bailey, S; de Barbaro, P; Barbaro-Galtieri, A; Barnes, V E; Barnett, B A; Baroiant, S; Barone, M; Bauer, G; Bedeschi, F; Belforte, S; Bell, W H; Bellettini, G; Bellinger, J; Benjamin, D; Bensinger, J; Beretvas, A; Berge, J P; Berryhill, J; Bevensee, B; Bhatti, A; Binkley, M; Bisello, D; Bishai, M; Blair, R E; Blocker, C; Bloom, K; Blumenfeld, B; Blusk, S R; Bocci, A; Bodek, A; Bokhari, W; Bolla, G; Bonushkin, Y; Bortoletto, D; Boudreau, J; Brandl, A; van den Brink, S; Bromberg, C; Brozovic, M; Bruner, N; Buckley-Geer, E; Budagov, J; Budd, H S; Burkett, K; Busetto, G; Byon-Wagner, A; Byrum, K L; Calafiura, P; Campbell, M; Carithers, W; Carlson, J; Carlsmith, D; Caskey, W; Cassada, J; Castro, A; Cauz, D; Cerri, A; Chan, A W; Chang, P S; Chang, P T; Chapman, J; Chen, C; Chen, Y C; Cheng, M T; Chertok, M; Chiarelli, G; Chirikov-Zorin, I; Chlachidze, G; Chlebana, F; Christofek, L; Chu, M L; Chung, Y S; Ciobanu, C I; Clark, A G; Connolly, A; Conway, J; Cordelli, M; Cranshaw, J; Cronin-Hennessy, D; Cropp, R; Culbertson, R; Dagenhart, D; D'Auria, S; DeJongh, F; Dell'Agnello, S; Dell'Orso, M; Demortier, L; Deninno, M; Derwent, P F; Devlin, T; Dittmann, J R; Donati, S; Done, J; Dorigo, T; Eddy, N; Einsweiler, K; Elias, J E; Engels, E; Erbacher, R; Errede, D; Errede, S; Fan, Q; Feild, R G; Fernandez, J P; Ferretti, C; Field, R D; Fiori, I; Flaugher, B; Foster, G W; Franklin, M; Freeman, J; Friedman, J; Fukui, Y; Furic, I; Galeotti, S; Gallinaro, M; Gao, T; Garcia-Sciveres, M; Garfinkel, A F; Gatti, P; Gay, C; Gerdes, D W; Giannetti, P; Giromini, P; Glagolev, V; Glenzinski, D; Gold, M; Goldstein, J; Gordon, A; Gorelov, I; Goshaw, A T; Gotra, Y; Goulianos, K; Green, C; Grim, G; Gris, P; Groer, L; Grosso-Pilcher, C; Guenther, M; Guillian, G; Da Costa, J G; Haas, R M; Haber, C; Hafen, E; Hahn, S R; Hall, C; Handa, T; Handler, R; Hao, W; Happacher, F; Hara, K; Hardman, A D; Harris, R M; Hartmann, F; Hatakeyama, K; Hauser, J; Heinrich, J; Heiss, A; Herndon, M; Hill, C; Hoffman, K D; Holck, C; Hollebeek, R; Holloway, L; Hughes, R; Huston, J; Huth, J; Ikeda, H; Incandela, J; Introzzi, G; Iwai, J; Iwata, Y; James, E; Jensen, H; Jones, M; Joshi, U; Kambara, H; Kamon, T; Kaneko, T; Karr, K; Kasha, H; Kato, Y; Keaffaber, T A; Kelley, K; Kelly, M; Kennedy, R D; Kephart, R; Khazins, D; Kikuchi, T; Kilminster, B; Kim, B J; Kim, D H; Kim, H S; Kim, M J; Kim, S H; Kim, Y K; Kirby, M; Kirk, M; Kirsch, L; Klimenko, S; Koehn, P; Köngeter, A; Kondo, K; Konigsberg, J; Kordas, K; Korn, A; Korytov, A; Kovacs, E; Kroll, J; Kruse, M; Kuhlmann, S E; Kurino, K; Kuwabara, T; Laasanen, A T; Lai, N; Lami, S; Lammel, S; Lamoureux, J I; Lancaster, J; Lancaster, M; Lander, R; Latino, G; LeCompte, T; Lee, A M; Lee, K; Leone, S; Lewis, J D; Lindgren, M; Liss, T M; Liu, J B; Liu, Y C; Litvintsev, D O; Lobban, O; Lockyer, N; Loken, J; Loreti, M; Lucchesi, D; Lukens, P; Lusin, S; Lyons, L; Lys, J; Madrak, R; Maeshima, K; Maksimovic, P; Malferrari, L; Mangano, M; Mariotti, M; Martignon, G; Martin, A; Matthews, J A; Mayer, J; Mazzanti, P; McFarland, K S; McIntyre, P; McKigney, E; Menguzzato, M; Menzione, A; Mesropian, C; Meyer, A; Miao, T; Miller, R; Miller, J S; Minato, H; Miscetti, S; Mishina, M; Mitselmakher, G; Moggi, N; Moore, E; Moore, R; Morita, Y; Moulik, T; Mulhearn, M; Mukherjee, A; Muller, T; Munar, A; Murat, P; Murgia, S; Nachtman, J; Nagaslaev, V; Nahn, S; Nakada, H; Nakaya, T; Nakano, I; Nelson, C; Nelson, T; Neu, C; Neuberger, D; Newman-Holmes, C; Ngan, C Y; Niu, H; Nodulman, L; Nomerotski, A; Oh, S H; Ohmoto, T; Ohsugi, T; Oishi, R; Okusawa, T; Olsen, J; Orejudos, W; Pagliarone, C; Palmonari, F; Paoletti, R; Papadimitriou, V; Pappas, S P; Partos, D; Patrick, J; Pauletta, G; Paulini, M; Paus, C; Pescara, L; Phillips, T J; Piacentino, G; Pitts, K T; Pompos, A; Pondrom, L; Pope, G; Popovic, M; Prokoshin, F; Proudfoot, J; Ptohos, F; Pukhov, O; Punzi, G; Ragan, K; Rakitine, A; Reher, D; Reichold, A; Ribon, A; Riegler, W; Rimondi, F; Ristori, L; Riveline, M; Robertson, W J; Robinson, A; Rodrigo, T; Rolli, S; Rosenson, L; Roser, R; Rossin, R; Roy, A; Safonov, A; St Denis, R; Sakumoto, W K; Saltzberg, D; Sanchez, C; Sansoni, A; Santi, L; Sato, H; Savard, P; Schlabach, P; Schmidt, E E; Schmidt, M P; Schmitt, M; Scodellaro, L; Scott, A; Scribano, A; Segler, S; Seidel, S; Seiya, Y; Semenov, A; Semeria, F; Shah, T; Shapiro, M D; Shepard, P F; Shibayama, T; Shimojima, M; Shochet, M; Siegrist, J; Sill, A; Sinervo, P; Singh, P; Slaughter, A J; Sliwa, K; Smith, C; Snider, F D; Solodsky, A; Spalding, J; Speer, T; Sphicas, P; Spinella, F; Spiropulu, M; Spiegel, L; Steele, J; Stefanini, A; Strologas, J; Strumia, F; Stuart, D; Sumorok, K; Suzuki, T; Takano, T; Takashima, R; Takikawa, K; Tamburello, P; Tartarelli, G F; Tanaka, M; Tannenbaum, B; Taylor, W; Tecchio, M; Tesarek, R; Teng, P K; Terashi, K; Tether, S; Thompson, A S; Thurman-Keup, R; Tipton, P; Tkaczyk, S; Tollefson, K; Tollestrup, A; Toyoda, H; Trischuk, W; de Troconiz, J F; Tseng, J; Turini, N; Ukegawa, F; Vaiciulis, T; Valls, J; Vejcik, S; Velev, G; Vidal, R; Vilar, R; Volobouev, I; Vucinic, D; Wagner, R G; Wagner, R L; Wahl, J; Wallace, N B; Walsh, A M; Wang, C; Wang, M J; Watanabe, T; Waters, D; Watts, T; Webb, R; Wenzel, H; Wester, W C; Wicklund, A B; Wicklund, E; Wilkes, T; Williams, H H; Wilson, P; Winer, B L; Winn, D; Wolbers, S; Wolinski, D; Wolinski, J; Wolinski, S; Worm, S; Wu, X; Wyss, J; Yagil, A; Yao, W; Yeh, G P; Yeh, P; Yoh, J; Yosef, C; Yoshida, T; Yu, I; Yu, S; Yu, Z; Zanetti, A; Zetti, F; Zucchelli, S

    2001-04-09

    We present the first measurement of the ratio of branching fractions R identical withB(t-->Wb)/B(t-->Wq) from p_p collisions at sqrt[s] = 1.8 TeV. The data set corresponds to 109 pb(-1) of data recorded by the Collider Detector at Fermilab during the 1992-95 Tevatron run. We measure R = 0.94(+0.31)(-0.24)(stat+syst) or R>0.61 (0.56) at 90% (95)% C.L., in agreement with the standard model predictions. This measurement yields a limit on the Cabibbo-Kobayashi-Maskawa quark mixing matrix element /V(tb)/ under the assumption of three generations and unitarity.

  15. Energy spectra of elements with 18 or = Z or = 28 between 10 and 300 GeV/amu

    NASA Technical Reports Server (NTRS)

    Jones, M. D.; Klarmann, J.; Stone, E. C.; Waddington, C. J.; Binns, W. R.; Garrard, T. L.; Israel, M. H.

    1985-01-01

    The HEAO-3 Heavy Nuclei Experiment is composed of ionization chambers above and below a plastic Cerenkov counter. The energy dependence of the abundances of elements with atomic number, Z, between 18 and 28 at very high energies where they are rare and thus need the large area x time are measured. The measurements of the Danish-French HEAO-3 experiment (Englemann,, et al., 1983) are extended to higher energies, using the relativistic rise of ionization signal as a measure of energy. Source abundances for Ar and Ca were determined.

  16. Nucleolar introns from Physarum flavicomum contain insertion elements that may explain how mobile group I introns gained their open reading frames.

    PubMed Central

    Vader, A; Naess, J; Haugli, K; Haugli, F; Johansen, S

    1994-01-01

    Comparison of two group I intron sequences in the nucleolar genome of the myxomycete Physarum flavicomum to their homologs in the closely related Physarum polycephalum revealed insertion-like elements. One of the insertion-like elements consists of two repetitive sequence motifs of 11 and 101 bp in five and three copies, respectively. The smaller motif, which flanks the larger, resembles a target duplication and indicates a relationship to transposons or retroelements. The insertion-like elements are found in the peripheral loops of the RNA structure; the positions occupied by the ORFs of mobile nucleolar group I introns. The P. flavicomum introns are 1184 and 637 bp in size, located in the large subunit ribosomal RNA gene, and can be folded into group I intron structures at the RNA level. However, the intron 2s from both P. flavicomum and P. polycephalum contain an unusual core region that lacks the P8 segment. None of the introns are able to self-splice in vitro. Southern analysis of different isolates indicates that the introns are not optional in myxomycetes. Images PMID:7984404

  17. V(D)J recombination frequency is affected by the sequence interposed between a pair of recombination signals: sequence comparison reveals a putative recombinational enhancer element.

    PubMed

    Roch, F A; Hobi, R; Berchtold, M W; Kuenzle, C C

    1997-06-15

    The immunoglobulin heavy chain intron enhancer (Emu) not only stimulates transcription but also V(D)J recombination of chromosomally integrated recombination substrates. We aimed at reproducing this effect in recombination competent cells by transient transfection of extrachromosomal substrates. These we prepared by interposing between the recombination signal sequences (RSS) of the plasmid pBlueRec various fragments, including Emu, possibly affecting V(D)J recombination. Our work shows that sequences inserted between RSS 23 and RSS 12, with distances from their proximal ends of 26 and 284 bp respectively, can markedly affect the frequency of V(D)J recombination. We report that the entire Emu, the Emu core as well as its flanking 5' and 3' matrix associated regions (5' and 3' MARs) upregulate V(D)J recombination while the downstream section of the 3' MAR of Emu does not. Also, prokaryotic sequences markedly suppress V(D)J recombination. This confirms previous results obtained with chromosomally integrated substrates, except for the finding that the full length 3' MAR of Emu stimulates V(D)J recombination in an episomal but not in a chromosomal context. The fact that other MARs do not share this activity suggests that the effect is no mediated through attachment of the recombination substrate to a nuclear matrix-associated recombination complex but through cis-activation. The presence of a 26 bp A-T-rich sequence motif in the 5' and 3' MARs of Emu and in all of the other upregulating fragments investigated, leads us to propose that the motif represents a novel recombinational enhancer element distinct from those constituting the Emu core.

  18. Precision Cross Sections Measurement of 56Fe(n,n γ) at 14.1 MeV using Associated Particle Neutron Elemental Imaging Technique

    NASA Astrophysics Data System (ADS)

    Wang, Haoyu; Koltick, David

    2017-01-01

    Integral production cross sections for 846.8 keV and 1238.3 keV prompt gamma rays from 14.1 MeV neutrons interactions on 56Fe and are reported, using Associated Particle Neutron Elemental Imaging technique. The experimental technique involves: (1) The development of a VME standard high speed DAQ system and a MATLAB parallel cluster for offline signal analysis with full control of data flow; (2) The advantage of the <1.5 ns coincidence timing resolution between the neutron production and the gamma ray detection to reject noise; (3) A large 30% solid angle gamma ray coverage by an array of NaI(Tl) detectors. The neutron flux is measured through detecting the associated alpha-particle from the D-T fusion reaction in the neutron generator. Present cross section measurements using other techniques with limited timing resolution and solid angle coverage are in agreement at neutron energies lower than 6 MeV. At higher neutron energies reported results can disagree by more than 20%. This more accurate technique presented can distinguish between the differences in the reported results based on pulse-mode neutron source and neutron time-of-flight techniques, at higher neutron energies.

  19. Respone to March 11, 2001 New York Public Interest Research Group, Inc. Comments on New York's Title V Program

    EPA Pesticide Factsheets

    This document may be of assistance in applying the Title V air operating permit regulations. This document is part of the Title V Policy and Guidance Database available at www2.epa.gov/title-v-operating-permits/title-v-operating-permit-policy-and-guidance-document-index. Some documents in the database are a scanned or retyped version of a paper photocopy of the original. Although we have taken considerable effort to quality assure the documents, some may contain typographical errors. Contact the office that issued the document if you need a copy of the original.

  20. V&V framework

    SciTech Connect

    Hills, Richard G.; Maniaci, David Charles; Naughton, Jonathan W.

    2015-09-01

    A Verification and Validation (V&V) framework is presented for the development and execution of coordinated modeling and experimental program s to assess the predictive capability of computational models of complex systems through focused, well structured, and formal processes.The elements of the framework are based on established V&V methodology developed by various organizations including the Department of Energy, National Aeronautics and Space Administration, the American Institute of Aeronautics and Astronautics, and the American Society of Mechanical Engineers. Four main topics are addressed: 1) Program planning based on expert elicitation of the modeling physics requirements, 2) experimental design for model assessment, 3) uncertainty quantification for experimental observations and computational model simulations, and 4) assessment of the model predictive capability. The audience for this document includes program planners, modelers, experimentalist, V &V specialist, and customers of the modeling results.

  1. CHARACTERIZING THE HEAVY ELEMENTS IN GLOBULAR CLUSTER M22 AND AN EMPIRICAL s-PROCESS ABUNDANCE DISTRIBUTION DERIVED FROM THE TWO STELLAR GROUPS

    SciTech Connect

    Roederer, I. U.; Marino, A. F.; Sneden, C.

    2011-11-20

    We present an empirical s-process abundance distribution derived with explicit knowledge of the r-process component in the low-metallicity globular cluster M22. We have obtained high-resolution, high signal-to-noise spectra for six red giants in M22 using the Magellan Inamori Kyocera Echelle spectrograph on the Magellan-Clay Telescope at Las Campanas Observatory. In each star we derive abundances for 44 species of 40 elements, including 24 elements heavier than zinc (Z = 30) produced by neutron-capture reactions. Previous studies determined that three of these stars (the 'r+s group') have an enhancement of s-process material relative to the other three stars (the 'r-only group'). We confirm that the r+s group is moderately enriched in Pb relative to the r-only group. Both groups of stars were born with the same amount of r-process material, but s-process material was also present in the gas from which the r+s group formed. The s-process abundances are inconsistent with predictions for asymptotic giant branch (AGB) stars with M {<=} 3 M{sub Sun} and suggest an origin in more massive AGB stars capable of activating the {sup 22}Ne({alpha},n){sup 25}Mg reaction. We calculate the s-process 'residual' by subtracting the r-process pattern in the r-only group from the abundances in the r+s group. In contrast to previous r- and s-process decompositions, this approach makes no assumptions about the r- and s-process distributions in the solar system and provides a unique opportunity to explore s-process yields in a metal-poor environment.

  2. Analytical microscopy observations of rat enterocytes after oral administration of soluble salts of lanthanides, actinides and elements of group III-A of the periodic chart.

    PubMed

    Floren, C; Tekaya, L; Escaig, F; Labejof, L; Mouthon, G; Galle, P

    2001-05-01

    The behavior in the intestinal barrier of nine elements (three of the group III-A, four lanthanides and two actinides), absorbed as soluble salts, has been studied by two microanalytical methods: electron probe X-ray micro analysis (EPMA) and secondary ion mass spectrometry (SIMS). It has been shown that the three elements of group III-A, aluminium, gallium and indium; and the four lanthanides, lanthanum, cerium, europium and thulium, are selectively concentrated and precipitated as non-soluble form in enterocytes of proximal part of the intestinal tract. SIMS microscopy has shown that these elements are concentrated as a number of submicroscopic precipitates, most of them localized in the apical part of the duodenum enterocytes, where they are observed from one hour to 48 hr after a single intragastric administration. No precipitate is observed after three days. It is suggested that this mechanism of local concentration limits the diffusion of these elements through the digestive barrier, some of them being toxic and none of them having a recognized physiological role. Additionally, the precipitation in duodenal enterocytes, the life time of which is on the order of 2-3 days, allows the elements absorbed as soluble form to be eliminated as a non-soluble form in the digestive lumen along with the desquamation of the apoptotic enterocytes. The intracytoplasmic localization of the precipitates are supposed to be the lysosomes although no direct evidence could be given here due to the very small sizes of the lysosomes of enterocytes. The same results were not observed with the two studied actinides. After administration of thorium, only some very sparse microprecipitates could be observed in intestinal mucosa and, after administration of uranium, no precipitates were observed with the exception of some in the conjunctive part of the duodenal villi.

  3. The frequency of factor V Leiden and prothrombin G20210A mutations in Slovak and Roma (Gypsy) ethnic group of Eastern Slovakia.

    PubMed

    Bôžiková, Alexandra; Gabriková, Dana; Sovičová, Adriana; Behulová, Regina; Mačeková, Soňa; Boroňová, Iveta; Petrejčíková, Eva; Soták, Miroslav; Bernasovská, Jarmila; Bernasovský, Ivan

    2012-10-01

    Factor V Leiden and prothrombin G20210A are the two most prevalent causes of inherited thrombophilia. The prevalence of these mutations varies widely in healthy Caucasian population. The aim of our study was to determine the frequency of factor V Leiden and prothrombin G20210A mutations in Slovak and Roma ethnic group from Eastern Slovakia. We analyzed 540 asymptomatic individuals (269 individuals of Slovak ethnicity and 271 individuals of Roma ethnicity) by real-time PCR method. The detected allele frequencies were 2.97 versus 6.64 % for factor V Leiden (p = 0.0049), and 0.74 versus 0.92 % for prothrombin mutation (p = 0.7463) in Slovak and Roma population, respectively. The Roma ethnic group had significantly higher prevalence of factor V Leiden mutation when compared to Slovak ethnic group. The allele frequency of factor V Leiden in ethnic Romanies from Eastern Slovakia was one of the highest in Europe. Our results confirm an uneven geographical and ethnic distribution of factor V Leiden.

  4. 1-Phenyl-3-methyl-4-benzoylpyrazol-5-one as a group-extraction reagent for spectrophotometric determination of trace elements.

    PubMed

    Mirza, M Y; Nwabue, F I

    1981-01-01

    1-Phenyl-3-methyl-4-benzoylpyrazol-5-one has been examined as a regent for detection and solvent extraction of metal ions. The reagent seems to be promising as a group-extraction reagent for the spectrophotometric determination of copper, nickel, cobalt, manganese, zinc, chromium(VI) and molybdenum(VI).

  5. Results of the Survey of RP Group Members: An Element in Strategic Planning for the Research & Planning Unit.

    ERIC Educational Resources Information Center

    Hom, Willard

    This document focuses on a stakeholder survey for a research unit. Although it covers just one part of the overall planning process that the Research & Planning (RP) Unit at the California Community Colleges Chancellor's Office, the researchers did survey other groups in the strategic planning effort. The stakeholder survey focused on four…

  6. Experimental design and optimization of leaching process for recovery of valuable chemical elements (U, La, V, Mo, Yb and Th) from low-grade uranium ore.

    PubMed

    Zakrzewska-Koltuniewicz, Grażyna; Herdzik-Koniecko, Irena; Cojocaru, Corneliu; Chajduk, Ewelina

    2014-06-30

    The paper deals with experimental design and optimization of leaching process of uranium and associated metals from low-grade, Polish ores. The chemical elements of interest for extraction from the ore were U, La, V, Mo, Yb and Th. Sulphuric acid has been used as leaching reagent. Based on the design of experiments the second-order regression models have been constructed to approximate the leaching efficiency of elements. The graphical illustrations using 3-D surface plots have been employed in order to identify the main, quadratic and interaction effects of the factors. The multi-objective optimization method based on desirability approach has been applied in this study. The optimum condition have been determined as P=5 bar, T=120 °C and t=90 min. Under these optimal conditions, the overall extraction performance is 81.43% (for U), 64.24% (for La), 98.38% (for V), 43.69% (for Yb) and 76.89% (for Mo) and 97.00% (for Th).

  7. Toxicity of arsenic (III) and (V) on plant growth, element uptake, and total amylolytic activity of mesquite (Prosopis juliflora x P. velutina).

    PubMed

    Mokgalaka-Matlala, Ntebogeng S; Flores-Tavizón, Edith; Castillo-Michel, Hiram; Peralta-Videa, Jose R; Gardea-Torresdey, Jorge L

    2008-01-01

    The effects of arsenite [As(III)] and arsenate [As(V)] on the growth of roots, stems, and leaves and the uptake of arsenic (As), micro- and macronutrients, and total amylolytic activity were investigated to elucidate the phytotoxicity of As to the mesquite plant (Prosopis juliflora x P. velutina). The plant growth was evaluated by measuring the root and shoot length, and the element uptake was determined using inductively coupled plasma optical emission spectroscopy. The root and leaf elongation decreased significantly with increasing As(III) and As(V) concentrations; whereas, stem elongation remained unchanged. The As uptake increased with increasing As(III) or As(V) concentrations in the medium. Plants treated with 50 mg/L As(III) accumulated up to 920 mg/kg dry weight (d wt) in roots and 522 mg/kg d wt in leaves, while plants exposed to 50 mg/L As(V) accumulated 1980 and 210 mg/kg d wt in roots and leaves, respectively. Increasing the As(V) concentration up to 20 mg/L resulted in a decrease in the total amylolytic activity. On the contrary, total amylolytic activity in As(III)-treated plants increased with increasing As concentration up to 20 mg/L. The macro- and micronutrient concentrations changed in As-treated plants. In shoots, Mo and K were reduced but Ca was increased, while in roots Fe and Ca were increased but K was reduced. These changes reduced the size of the plants, mainly in the As(III)-treated plants; however, there were no visible sign of As toxicity.

  8. L shell x ray production in high-Z elements using 4-6 MeV/u fluorine ions

    NASA Astrophysics Data System (ADS)

    Kumar, Sunil; Singh, Udai; Oswal, M.; Singh, G.; Singh, N.; Mehta, D.; Nandi, T.; Lapicki, G.

    2017-03-01

    L shell line and total x ray production cross sections in 78Pt, 79Au, 82Pb, 83Bi, 90Th, and 92U targets ionized by 4-6 MeV/u fluorine ions were measured. These cross sections are compared with available theories for L shell ionization using single- and multiple-hole fluorescence and the Coster-Kronig yields. The ECPSSR and the ECUSAR theories exhibit good agreement with the measured data, whereas, the FBA theory overestimates them by a factor of two. Although for the F ion charge states q = 6-8 the multiple-hole atomic parameters do not significantly differ from the single-hole values, after an account for the multiple-holes, our data are better in agreement with the ECUSAR than the ECPSSR theory.

  9. 2D finite element model and microstructural changes during cutting of Ti6Al4V in dry condition

    NASA Astrophysics Data System (ADS)

    Imbrogno, Stano; Rinaldi, Sergio; Seara, Borja; Arrazola, Pedro J.; Rotella, Giovanna; Umbrello, Domenico

    2016-10-01

    The main objective of this study is to develop a FE model of the orthogonal cutting process executed on Titanium alloy (Ti6Al4V) under dry condition. In detail, the Abaqus/Explicit 2D formulation has been used to simulate the process and the results provided (temperature and strain rate) where employed to calculate the microstructural and hardness changes on surface and sub-surface. The quantitative analysis in terms of the grain refinement and hardness variation during the cutting process has been provided taking into account the Zener-Hollomon and Hall-Petch equations. The obtained results were compared with the experimental outcomes in order to understand the reliable rate of the model.

  10. Population-based dietary intakes and tap water concentrations for selected elements in the EPA region V National Human Exposure Assessment Survey (NHEXAS).

    PubMed

    Thomas, K W; Pellizzari, E D; Berry, M R

    1999-01-01

    A National Human Exposure Assessment Survey (NHEXAS) field study was performed in U.S. Environmental Protection Agency (EPA) Region V, providing population-based exposure distribution data for selected elements in several personal, environmental, and biological media. Population distributions are reported for the 11 elements that were measured in water and dietary samples. Dietary intakes and home tap water concentrations of lead, arsenic, and cadmium were further examined for intermedia associations, for differences between dietary exposure for adults and children, and to estimate the proportion of the population above health-based reference values (dietary) or regulatory action levels or maximum contaminant levels (water). Water lead and arsenic concentrations were significantly associated with dietary intake. Intake of all elements was higher from solid foods than from liquid foods (including drinking water). Dietary intakes of Pb, As, and Cd were greater than those calculated for intake from home tap water or inhalation on a microg/day basis. Median dietary intakes for the Region V population for Pb, As, and Cd were 0.10, 0.13, and 0.19 microg/kg bw/day, respectively. While Pb, As, and Cd concentrations in the foods consumed by 0 to 6-year-old children were similar to or lower than those for adults, dietary intakes calculated on a body weight basis were 1.5 to 2.5 times higher for young children. Intrapersonal intake differences accounted for most of the variance in short-term (daily) dietary intakes for Pb and As, while interpersonal differences accounted for more of the intake variance for Cd. Only small percentages of the population exceeded health-based intake reference values or concentrations equal to regulatory levels in water for Pb, As, and Cd.

  11. III-V arsenide-nitride semiconductor

    NASA Technical Reports Server (NTRS)

    Major, Jo S. (Inventor); Welch, David F. (Inventor); Scifres, Donald R. (Inventor)

    2000-01-01

    III-V arsenide-nitride semiconductor are disclosed. Group III elements are combined with group V elements, including at least nitrogen and arsenic, in concentrations chosen to lattice match commercially available crystalline substrates. Epitaxial growth of these III-V crystals results in direct bandgap materials, which can be used in applications such as light emitting diodes and lasers. Varying the concentrations of the elements in the III-V materials varies the bandgaps, such that materials emitting light spanning the visible spectra, as well as mid-IR and near-UV emitters, can be created. Conversely, such material can be used to create devices that acquire light and convert the light to electricity, for applications such as full color photodetectors and solar energy collectors. The growth of the III-V material can be accomplished by growing thin layers of elements or compounds in sequences that result in the overall lattice match and bandgap desired.

  12. [Molecular evolution of mobile elements of the gypsy group: a homolog of the gag gene in Drosophila].

    PubMed

    Nefedova, L N; Kim, A I

    2009-01-01

    Retrotransposons of the gypsy group of Drosophila melanogaster that are structurally similar to retroviruses of vertebrates occupy an important place among retroelements of eukaryotes. The infectious abilities of some retrotransposons of this group (gypsy, ZAM, and Idefix) have been demonstrated experimentally, and therefore they are true retroviruses. It is supposed that retrotransposons can evolve acquiring new components, the sources of which remain to be elucidated. In this work, the CG4680 gene (Gag related protein, Grp) homologous to gag of retrotransposons of the gypsy group has been identified in the genome of D. melanogaster and characterized. The Grp gene product has a highly conserved structure in different species of the Drosophilidae family and is under of stabilizing selection, which suggests its important genomic function in Drosophila. In view of the earlier data, it can be concluded that homologous genes of all components of gypsy retrotransposons are present in the Drosophila genome. These genes can be both precursors and products of domestication of retrovirus genes.

  13. Cloning, expression and characterization of mugwort pollen allergen Art v 2, a pathogenesis-related protein from family group 1.

    PubMed

    Arilla, M C; Ibarrola, I; Puente, Y; Daza, J C; Martínez, A; Asturias, J A

    2007-07-01

    Mugwort (Artemisia vulgaris) belongs to the Compositae family, and is one of the main causes of allergy in late summer and autumn. The aim of the study was to characterize the allergen Art v 2 from mugwort pollen. Skin prick tests, performed in 19 patients allergic to mugwort and 10 control patients, showed an Art v 2 sensitization prevalence of 58%, whereas none false-positives were detected among control patients. Art v 2 was purified by standard chromatography and binding to Concanavalin A column and had an apparent molecular mass of 33 and 20 kDa, calculated by gel permeation and SDS-PAGE under denaturing conditions, respectively, showing that the allergen is composed of two identical subunits. Art v 2-encoding cDNA was amplified by PCR using degenerate primers based on reported partial amino acid sequences. Cloned cDNA encoding Art v 2 contains 140 bp that codify for a polypeptide of 15.8 kDa, with a predicted pI value of 5.2, and one potential N-glycosylation site. Protein homology search demonstrated that Art v 2 share 55-42% identical residues with pathogenesis-related protein PR-1 of tomato, potato, rape, wheat and rice. Homology was also found to Ves v 5 (41% identical residues). Bacterial-expressed recombinant Art v 2 was recognized only by 21% of mugwort-allergic patients. In conclusion, Art v 2 from mugwort is the first weed pollen allergen that belongs to the pathogenesis-related protein PR-1 and its recombinant form could help molecular diagnosis of mugwort associated allergy.

  14. Coupled Transient Finite Element Simulation of Quench in Jefferson Lab's 11 GeV Super High Momentum Spectrometer Superconducting Magnets

    SciTech Connect

    E. Sun, P. Brindza, S. Lassiter, M. Fowler, E. Xu

    2010-06-01

    This paper presents coupled transient thermal and electromagnetic finite element analysis of quench in the Q2, Q3, and dipole superconducting magnets using Vector Fields Quench code. Detailed temperature distribution within coils and aluminum force collars were computed at each time step. Both normal (quench with dump resistor) and worst-case (quench without dump resistor) scenarios were simulated to investigate the maximum temperatures. Two simulation methods were utilized, and their algorithms, implementation, advantages, and disadvantages are discussed. The first method simulated the coil using nonlinear transient thermal analysis directly linked with the transient circuit analysis. It was faster because only the coil was meshed and no eddy current was modeled. The second method simulated the whole magnet including the coil, the force collar, and the iron yoke. It coupled thermal analysis with transient electromagnetic field analysis which modeled electromagnetic fields including eddy currents within the force collar. Since eddy currents and temperature in the force collars were calculated in various configurations, segmentation of the force collars was optimized under the condition of fast discharge.

  15. GEANT4 Simulation of Hadronic Interactions at 8-GeV/C to 10-GeV/C: Response to the HARP-CDP Group

    SciTech Connect

    Uzhinsky, V.; Apostolakis, J.; Folger, G.; Ivanchenko, V.N.; Kossov, M.V.; Wright, D.H.; /SLAC

    2011-11-21

    The results of the HARP-CDP group on the comparison of GEANT4 Monte Carlo predictions versus experimental data are discussed. It is shown that the problems observed by the group are caused by an incorrect implementation of old features at the programming level, and by a lack of the nucleon Fermi motion in the simulation of quasielastic scattering. These drawbacks are not due to the physical models used. They do not manifest themselves in the most important applications of the GEANT4 toolkit.

  16. Top quark mass measurement in the t tmacr all hadronic channel using a matrix element technique in p pmacr collisions at s=1.96TeV

    NASA Astrophysics Data System (ADS)

    Aaltonen, T.; Adelman, J.; Akimoto, T.; González, B. Álvarez; Amerio, S.; Amidei, D.; Anastassov, A.; Annovi, A.; Antos, J.; Apollinari, G.; Apresyan, A.; Arisawa, T.; Artikov, A.; Ashmanskas, W.; Attal, A.; Aurisano, A.; Azfar, F.; Azzurri, P.; Badgett, W.; Barbaro-Galtieri, A.; Barnes, V. E.; Barnett, B. A.; Bartsch, V.; Bauer, G.; Beauchemin, P.-H.; Bedeschi, F.; Beecher, D.; Behari, S.; Bellettini, G.; Bellinger, J.; Benjamin, D.; Beretvas, A.; Beringer, J.; Bhatti, A.; Binkley, M.; Bisello, D.; Bizjak, I.; Blair, R. E.; Blocker, C.; Blumenfeld, B.; Bocci, A.; Bodek, A.; Boisvert, V.; Bolla, G.; Bortoletto, D.; Boudreau, J.; Boveia, A.; Brau, B.; Bridgeman, A.; Brigliadori, L.; Bromberg, C.; Brubaker, E.; Budagov, J.; Budd, H. S.; Budd, S.; Burke, S.; Burkett, K.; Busetto, G.; Bussey, P.; Buzatu, A.; Byrum, K. L.; Cabrera, S.; Calancha, C.; Campanelli, M.; Campbell, M.; Canelli, F.; Canepa, A.; Carls, B.; Carlsmith, D.; Carosi, R.; Carrillo, S.; Carron, S.; Casal, B.; Casarsa, M.; Castro, A.; Catastini, P.; Cauz, D.; Cavaliere, V.; Cavalli-Sforza, M.; Cerri, A.; Cerrito, L.; Chang, S. H.; Chen, Y. C.; Chertok, M.; Chiarelli, G.; Chlachidze, G.; Chlebana, F.; Cho, K.; Chokheli, D.; Chou, J. P.; Choudalakis, G.; Chuang, S. H.; Chung, K.; Chung, W. H.; Chung, Y. S.; Chwalek, T.; Ciobanu, C. I.; Ciocci, M. A.; Clark, A.; Clark, D.; Compostella, G.; Convery, M. E.; Conway, J.; Cordelli, M.; Cortiana, G.; Cox, C. A.; Cox, D. J.; Crescioli, F.; Cuenca Almenar, C.; Cuevas, J.; Culbertson, R.; Cully, J. C.; Dagenhart, D.; Datta, M.; Davies, T.; de Barbaro, P.; de Cecco, S.; Deisher, A.; de Lorenzo, G.; Dell'Orso, M.; Deluca, C.; Demortier, L.; Deng, J.; Deninno, M.; Derwent, P. F.; di Giovanni, G. P.; Dionisi, C.; di Ruzza, B.; Dittmann, J. R.; D'Onofrio, M.; Donati, S.; Dong, P.; Donini, J.; Dorigo, T.; Dube, S.; Efron, J.; Elagin, A.; Erbacher, R.; Errede, D.; Errede, S.; Eusebi, R.; Fang, H. C.; Farrington, S.; Fedorko, W. T.; Feild, R. G.; Feindt, M.; Fernandez, J. P.; Ferrazza, C.; Field, R.; Flanagan, G.; Forrest, R.; Frank, M. J.; Franklin, M.; Freeman, J. C.; Furic, I.; Gallinaro, M.; Galyardt, J.; Garberson, F.; Garcia, J. E.; Garfinkel, A. F.; Genser, K.; Gerberich, H.; Gerdes, D.; Gessler, A.; Giagu, S.; Giakoumopoulou, V.; Giannetti, P.; Gibson, K.; Gimmell, J. L.; Ginsburg, C. M.; Giokaris, N.; Giordani, M.; Giromini, P.; Giunta, M.; Giurgiu, G.; Glagolev, V.; Glenzinski, D.; Gold, M.; Goldschmidt, N.; Golossanov, A.; Gomez, G.; Gomez-Ceballos, G.; Goncharov, M.; González, O.; Gorelov, I.; Goshaw, A. T.; Goulianos, K.; Gresele, A.; Grinstein, S.; Grosso-Pilcher, C.; Group, R. C.; Grundler, U.; Guimaraes da Costa, J.; Gunay-Unalan, Z.; Haber, C.; Hahn, K.; Hahn, S. R.; Halkiadakis, E.; Han, B.-Y.; Han, J. Y.; Happacher, F.; Hara, K.; Hare, D.; Hare, M.; Harper, S.; Harr, R. F.; Harris, R. M.; Hartz, M.; Hatakeyama, K.; Hays, C.; Heck, M.; Heijboer, A.; Heinrich, J.; Henderson, C.; Herndon, M.; Heuser, J.; Hewamanage, S.; Hidas, D.; Hill, C. S.; Hirschbuehl, D.; Hocker, A.; Hou, S.; Houlden, M.; Hsu, S.-C.; Huffman, B. T.; Hughes, R. E.; Husemann, U.; Hussein, M.; Husemann, U.; Huston, J.; Incandela, J.; Introzzi, G.; Iori, M.; Ivanov, A.; James, E.; Jayatilaka, B.; Jeon, E. J.; Jha, M. K.; Jindariani, S.; Johnson, W.; Jones, M.; Joo, K. K.; Jun, S. Y.; Jung, J. E.; Junk, T. R.; Kamon, T.; Kar, D.; Karchin, P. E.; Kato, Y.; Kephart, R.; Keung, J.; Khotilovich, V.; Kilminster, B.; Kim, D. H.; Kim, H. S.; Kim, H. W.; Kim, J. E.; Kim, M. J.; Kim, S. B.; Kim, S. H.; Kim, Y. K.; Kimura, N.; Kirsch, L.; Klimenko, S.; Knuteson, B.; Ko, B. R.; Kondo, K.; Kong, D. J.; Konigsberg, J.; Korytov, A.; Kotwal, A. V.; Kreps, M.; Kroll, J.; Krop, D.; Krumnack, N.; Kruse, M.; Krutelyov, V.; Kubo, T.; Kuhr, T.; Kulkarni, N. P.; Kurata, M.; Kwang, S.; Laasanen, A. T.; Lami, S.; Lammel, S.; Lancaster, M.; Lander, R. L.; Lannon, K.; Lath, A.; Latino, G.; Lazzizzera, I.; Lecompte, T.; Lee, E.; Lee, H. S.; Lee, S. W.; Leone, S.; Lewis, J. D.; Lin, C.-S.; Linacre, J.; Lindgren, M.; Lipeles, E.; Lister, A.; Litvintsev, D. O.; Liu, C.; Liu, T.; Lockyer, N. S.; Loginov, A.; Loreti, M.; Lovas, L.; Lucchesi, D.; Luci, C.; Lueck, J.; Lujan, P.; Lukens, P.; Lungu, G.; Lyons, L.; Lys, J.; Lysak, R.; MacQueen, D.; Madrak, R.; Maeshima, K.; Makhoul, K.; Maki, T.; Maksimovic, P.; Malde, S.; Malik, S.; Manca, G.; Manousakis-Katsikakis, A.; Margaroli, F.; Marino, C.; Marino, C. P.; Martin, A.; Martin, V.; Martínez, M.; Martínez-Ballarín, R.; Maruyama, T.; Mastrandrea, P.; Masubuchi, T.; Mathis, M.; Mattson, M. E.; Mazzanti, P.; McFarland, K. S.; McIntyre, P.; McNulty, R.; Mehta, A.; Mehtala, P.; Menzione, A.; Merkel, P.; Mesropian, C.; Miao, T.; Miladinovic, N.; Miller, R.; Mills, C.; Milnik, M.; Mitra, A.; Mitselmakher, G.; Miyake, H.; Moggi, N.; Moon, C. S.; Moore, R.; Morello, M. J.; Morlok, J.; Movilla Fernandez, P.; Mülmenstädt, J.; Mukherjee, A.; Muller, Th.; Mumford, R.; Murat, P.; Mussini, M.; Nachtman, J.; Nagai, Y.; Nagano, A.; Naganoma, J.; Nakamura, K.; Nakano, I.; Napier, A.; Necula, V.; Nett, J.; Neu, C.; Neubauer, M. S.; Neubauer, S.; Nielsen, J.; Nodulman, L.; Norman, M.; Norniella, O.; Nurse, E.; Oakes, L.; Oh, S. H.; Oh, Y. D.; Oksuzian, I.; Okusawa, T.; Orava, R.; Pagan Griso, S.; Palencia, E.; Papadimitriou, V.; Papaikonomou, A.; Paramonov, A. A.; Parks, B.; Pashapour, S.; Patrick, J.; Pauletta, G.; Paulini, M.; Paus, C.; Peiffer, T.; Pellett, D. E.; Penzo, A.; Phillips, T. J.; Piacentino, G.; Pianori, E.; Pinera, L.; Pitts, K.; Plager, C.; Pondrom, L.; Poukhov, O.; Pounder, N.; Prakoshyn, F.; Pronko, A.; Proudfoot, J.; Ptohos, F.; Pueschel, E.; Punzi, G.; Pursley, J.; Rademacker, J.; Rahaman, A.; Ramakrishnan, V.; Ranjan, N.; Redondo, I.; Renton, P.; Renz, M.; Rescigno, M.; Richter, S.; Rimondi, F.; Ristori, L.; Robson, A.; Rodrigo, T.; Rodriguez, T.; Rogers, E.; Rolli, S.; Roser, R.; Rossi, M.; Rossin, R.; Roy, P.; Ruiz, A.; Russ, J.; Rusu, V.; Safonov, A.; Sakumoto, W. K.; Saltó, O.; Santi, L.; Sarkar, S.; Sartori, L.; Sato, K.; Savoy-Navarro, A.; Schlabach, P.; Schmidt, A.; Schmidt, E. E.; Schmidt, M. A.; Schmidt, M. P.; Schmitt, M.; Schwarz, T.; Scodellaro, L.; Scribano, A.; Scuri, F.; Sedov, A.; Seidel, S.; Seiya, Y.; Semenov, A.; Sexton-Kennedy, L.; Sforza, F.; Sfyrla, A.; Shalhout, S. Z.; Shears, T.; Shepard, P. F.; Shimojima, M.; Shiraishi, S.; Shochet, M.; Shon, Y.; Shreyber, I.; Sidoti, A.; Sinervo, P.; Sisakyan, A.; Slaughter, A. J.; Slaunwhite, J.; Sliwa, K.; Smith, J. R.; Snider, F. D.; Snihur, R.; Soha, A.; Somalwar, S.; Sorin, V.; Spalding, J.; Spreitzer, T.; Squillacioti, P.; Stanitzki, M.; St. Denis, R.; Stelzer, B.; Stelzer-Chilton, O.; Stentz, D.; Strologas, J.; Strycker, G. L.; Stuart, D.; Suh, J. S.; Sukhanov, A.; Suslov, I.; Suzuki, T.; Taffard, A.; Takashima, R.; Takeuchi, Y.; Tanaka, R.; Tecchio, M.; Teng, P. K.; Terashi, K.; Thom, J.; Thompson, A. S.; Thompson, G. A.; Thomson, E.; Tipton, P.; Ttito-Guzmán, P.; Tkaczyk, S.; Toback, D.; Tokar, S.; Tollefson, K.; Tomura, T.; Tonelli, D.; Torre, S.; Torretta, D.; Totaro, P.; Tourneur, S.; Trovato, M.; Tsai, S.-Y.; Tu, Y.; Turini, N.; Ukegawa, F.; Vallecorsa, S.; van Remortel, N.; Varganov, A.; Vataga, E.; Vázquez, F.; Velev, G.; Vellidis, C.; Vidal, M.; Vidal, R.; Vila, I.; Vilar, R.; Vine, T.; Vogel, M.; Volobouev, I.; Volpi, G.; Wagner, P.; Wagner, R. G.; Wagner, R. L.; Wagner, W.; Wagner-Kuhr, J.; Wakisaka, T.; Wallny, R.; Wang, S. M.; Warburton, A.; Waters, D.; Weinberger, M.; Weinelt, J.; Wester, W. C., III; Whitehouse, B.; Whiteson, D.; Wicklund, A. B.; Wicklund, E.; Wilbur, S.; Williams, G.; Williams, H. H.; Wilson, P.; Winer, B. L.; Wittich, P.; Wolbers, S.; Wolfe, C.; Wright, T.; Wu, X.; Würthwein, F.; Xie, S.; Yagil, A.; Yamamoto, K.; Yamaoka, J.; Yang, U. K.; Yang, Y. C.; Yao, W. M.; Yeh, G. P.; Yoh, J.; Yorita, K.; Yoshida, T.; Yu, G. B.; Yu, I.; Yu, S. S.; Yun, J. C.; Zanello, L.; Zanetti, A.; Zhang, X.; Zheng, Y.; Zucchelli, S.; CDF Collaboration

    2009-04-01

    We present a measurement of the top quark mass in the all hadronic channel (t tmacr →b bmacr q1 qmacr 2q3 qmacr 4) using 943pb-1 of p pmacr collisions at s=1.96TeV collected at the CDF II detector at Fermilab (CDF). We apply the standard model production and decay matrix element (ME) to t tmacr candidate events. We calculate per-event probability densities according to the ME calculation and construct template models of signal and background. The scale of the jet energy is calibrated using additional templates formed with the invariant mass of pairs of jets. These templates form an overall likelihood function that depends on the top quark mass and on the jet energy scale (JES). We estimate both by maximizing this function. Given 72 observed events, we measure a top quark mass of 171.1±3.7(stat+JES)±2.1(syst)GeV/c2. The combined uncertainty on the top quark mass is 4.3GeV/c2.

  17. Properties and reactivity patterns of AsP(3): an experimental and computational study of group 15 elemental molecules.

    PubMed

    Cossairt, Brandi M; Cummins, Christopher C

    2009-10-28

    Facile synthetic access to the isolable, thermally robust AsP(3) molecule has allowed for a thorough study of its physical properties and reaction chemistry with a variety of transition-metal and organic fragments. The electronic properties of AsP(3) in comparison with P(4) are revealed by DFT and atoms in molecules (AIM) approaches and are discussed in relation to the observed electrochemical profiles and the phosphorus NMR properties of the two molecules. An investigation of the nucleus independent chemical shifts revealed that AsP(3) retains spherical aromaticity. The thermodynamic properties of AsP(3) and P(4) are described. The reaction types explored in this study include the thermal decomposition of the AsP(3) tetrahedron to its elements, the synthesis and structural characterization of [(AsP(3))FeCp*(dppe)][BPh(4)] (dppe = 1,2-bis(diphenylphosphino)ethane), 1, selective single As-P bond cleavage reactions, including the synthesis and structural characterization of AsP(3)(P(N((i)Pr)(2))N(SiMe(3))(2))(2), 2, and activations of AsP(3) by reactive early transition-metal fragments including Nb(H)(eta(2)-(t)Bu(H)C horizontal lineNAr)(N[CH(2)(t)Bu]Ar)(2) and Mo(N[(t)Bu]Ar)(3) (Ar = 3,5-Me(2)C(6)H(3)). In the presence of reducing equivalents, AsP(3) was found to allow access to [Na][E(3)Nb(ODipp)(3)] (Dipp = 2,6-diisopropylphenyl) complexes (E = As or P) which themselves allow access to mixtures of As(n)P(4-n) (n = 1-4).

  18. Synthesis, surface group modification of 3D MnV{sub 2}O{sub 6} nanostructures and adsorption effect on Rhodamine B

    SciTech Connect

    Zhang, Wanqun; Shi, Lei; Tang, Kaibin; Liu, Zhongping

    2012-07-15

    Highlights: ► Fabrication of urchin-like MnV{sub 2}O{sub 6} with oxygen-containing surface groups. ► Mn{sub 0.5}V{sub 2}O{sub 5}·nH{sub 2}O as an intermediate product holds the key to the final products. ► 3D architectures of MnV{sub 2}O{sub 6} with oxygen-containing surface groups as sorbent. ► The sorbent shows a good adsorption ability. -- Abstract: Highly uniform 3D MnV{sub 2}O{sub 6} nanostructures modified by oxygen functional groups (-COO-) were successfully prepared in large quantities by an approach involving preparation of vanadyl ethylene glycolate as the precursor. The growth and self-assembly of MnV{sub 2}O{sub 6} nanobelts and nanorods could be readily tuned by additive species and quantities, which brought different morphologies and sizes to the final products. With a focus on the regulation of structure, the formation process of 3D architectures of MnV{sub 2}O{sub 6} by self-assembly of nanobelts was followed by field emission scanning electron microscopy (FE-SEM) and X-ray diffraction (XRD). The consecutive processes of vanadyl ethylene glycolate and benzoyl peroxide assisted formation of layered structure Mn{sub 0.5}V{sub 2}O{sub 5}·nH{sub 2}O, growth of aligned MnV{sub 2}O{sub 6} nanobelts, and oriented assembly were proposed for the growth mechanism. The band gap vs. different morphology was also studied. Optical characterization of these MnV{sub 2}O{sub 6} with different morphologies showed direct bandgap energies at 1.8–1.95 eV. The adsorption properties of 3D MnV{sub 2}O{sub 6} nanostructures synthesized under different conditions were investigated through the removal test of Rhodamine B in aqueous water, and the 3D nanostructures synthesized with 30 g L{sup −1} benzoyl peroxide showed good adsorption capability of Rhodamine B.

  19. 75 FR 45623 - Morris Energy Group, LLC v.PSEG Energy Resources & Trade LLC; PSEG Fossil LLC; and PSEG Power LLC...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-08-03

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF ENERGY Federal Energy Regulatory Commission Morris Energy Group, LLC v.PSEG Energy Resources & Trade LLC; PSEG Fossil..., LLC, PSEG Fossil LLC and PSEG Power LLC (PSEG Power Companies) (Respondents), requesting that...

  20. Muon groups and primary composition at 10 to the 13th power to 10 to the 15th power eV

    NASA Technical Reports Server (NTRS)

    Budko, E. V.; Chudakov, A. E.; Dogujaev, V. A.; Mihelev, A. R.; Padey, V. A.; Petkov, V. A.; Striganov, P. S.; Suvorova, O. V.; Voevodsky, A. V.

    1985-01-01

    The data on muon groups observed at Baksan underground scintillation telescope is analyzed. In this analysis we compare the experimental data with calulations, based on a superposition model in order to obtain the effective atomic number of primary cosmic rays in the energy range 10 to the 13th power to 10 to the 15th power eV.

  1. 76 FR 46793 - PJM Interconnection, L.L.C.; PJM Power Providers Group v. PJM Interconnection, L.L.C.; Notice...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-08-03

    ... Energy Regulatory Commission PJM Interconnection, L.L.C.; PJM Power Providers Group v. PJM Interconnection, L.L.C.; Notice Establishing Post-Technical Comment Period As indicated in the June 29, 2011... issues related to PJM Interconnection, L.L.C. (PJM)'s Minimum Offer Price Rule (MOPR) and...

  2. ENVIRONMENTAL TECHNOLOGY VERIFICATION, TEST REPORT OF CONTROL OF BIOAEROSOLS IN HVAC SYSTEMS, FILTRATION GROUP, AEROSTAR FP-98 MINIPLEAT V-BLANK FILTER

    EPA Science Inventory

    The Environmental Technology Verification report discusses the technology and performance of the AeroStar FP-98 Minipleat V-Bank Filter air filter for dust and bioaerosol filtration manufactured by Filtration Group. The pressure drop across the filter was 137 Pa clean and 348 Pa ...

  3. Role of group V phospholipase A2 in zymosan-induced eicosanoid generation and vascular permeability revealed by targeted gene disruption*

    PubMed Central

    Satake, Yoshiyuki; Diaz, Bruno L.; Balestrieri, Barbara; Lam, Bing K.; Kanaoka, Yoshihide; Grusby, Michael J.; Arm, Jonathan P.

    2005-01-01

    SUMMARY Conclusions regarding the contribution of low molecular weight secretory phospholipase A2 (sPLA2) enzymes in eicosanoid generation have relied on data obtained from transfected cells or the use of inhibitors that fail to discriminate between individual members of the large family of mammalian sPLA2 enzymes. To elucidate the role of group V sPLA2, we used targeted gene disruption to generate mice lacking this enzyme. Zymosan-induced generation of leukotriene C4 and prostaglandin E2 was attenuated ~50% in peritoneal macrophages from group V sPLA2-null mice compared to macrophages from wild-type littermates. Furthermore, the early phase of plasma exudation in response to intraperitoneal injection of zymosan and the accompanying in vivo generation of cysteinyl leukotrienes were markedly attenuated in group V sPLA2-null mice compared to wild-type controls. These data provide clear evidence of a role for group V sPLA2 in regulating eicosanoid generation in response to an acute innate stimulus of the immune response both in vitro and in vivo, suggesting a role for this enzyme in innate immunity. PMID:14761945

  4. Bonds, bands, and band gaps in tetrahedrally bonded ternary compounds: The role of group V lone pairs

    NASA Astrophysics Data System (ADS)

    Do, Dat T.; Mahanti, S. D.

    2014-04-01

    An interesting class of tetrahedrally coordinated ternary compounds has attracted considerable interest because of their potential as good thermoelectrics. These compounds, denoted as I3-V-VI4, contain three monovalent-I (Cu, Ag), one nominally pentavalent-V (P, As, Sb, Bi), and four hexavalent-VI (S, Se, Te) atoms; and can be visualized as ternary derivatives of the II-VI zincblende or wurtzite semiconductors, obtained by starting from four unit cells of (II-VI) and replacing four type II atoms by three type I and one type V atoms. We find that nominally pentavalent-V atoms are effectively trivalent and their lone (ns2) pairs play an active role in opening up a gap. The lowest conduction band is a strongly hybridized anti-bonding combination of the lone pair and chalcogen (VI) p-states. The magnitude of the gap is sensitive to the nature of the exchange interaction (local vs non-local) and the V-VI distance. We also find that the electronic structure near the gap can be reproduced extremely well within a local theory if one can manipulate the position of the filled d bands of Cu and Ag by an effectively large U.

  5. The marriage of metallacycle transfer chemistry with Suzuki-Miyaura cross-coupling to give main group element-containing conjugated polymers.

    PubMed

    He, Gang; Kang, Le; Torres Delgado, William; Shynkaruk, Olena; Ferguson, Michael J; McDonald, Robert; Rivard, Eric

    2013-04-10

    A versatile and general synthetic route for the synthesis of conjugated main group element-based polymers, previously inaccessible by conventional means, is reported. These polymers contain five-membered chalcogenophene rings based on S, Se, and Te, and we demonstrate that optoelectronic properties can be readily tuned via controlled atom substitution chemistry. In addition, regioregular hybrid thiophene-selenophene-tellurophene and selenophene-fluorene copolymers were synthesized to provide a further illustration of the scope of the presented metallacycle transfer/cross-coupling polymerization method.

  6. Measurement of the t-channel single-top-quark production cross section and of the $\\mid V_{tb} \\mid$ CKM matrix element in pp collisions at $\\sqrt{s}$= 8 TeV

    SciTech Connect

    Khachatryan, Vardan

    2014-06-16

    Our measurements are presented of the t-channel single-top-quark production cross section in proton-proton collisions at √s = 8 TeV. The results are based on a data sample corresponding to an integrated luminosity of 19.7 fb-1 recorded with the CMS detector at the LHC. The cross section is measured inclusively, as well as separately for top (t) and antitop (t¯), in final states with a muon or an electron. The measured inclusive t-channel cross section is σ t-ch. = 83.6 ± 2.3 (stat.) ± 7.4 (syst.) pb. The single t and t¯ cross sections are measured to be σ t-ch.(t) = 53.8 ± 1.5 (stat.) ± 4.4 (syst.) pb and σ t-ch. (t¯) = 27.6 ± 1.3 (stat.) ± 3.7 (syst.) pb, respectively. The measured ratio of cross sections is R t-ch. = σ t-ch.(t)/σ t-ch. (t¯) = 1.95 ± 0.10 (stat.) ± 0.19 (syst.), in agreement with the standard model prediction. Finally, the modulus of the Cabibbo-Kobayashi-Maskawa matrix element V tb is extracted and, in combination with a previous CMS result at √s = 7 TeV, a value |V tb| = 0.998 ± 0.038 (exp.) ± 0.016 (theo.) is obtained.

  7. Measurement of the t-channel single-top-quark production cross section and of the $$\\mid V_{tb} \\mid$$ CKM matrix element in pp collisions at $$\\sqrt{s}$$= 8 TeV

    DOE PAGES

    Khachatryan, Vardan

    2014-06-16

    Our measurements are presented of the t-channel single-top-quark production cross section in proton-proton collisions at √s = 8 TeV. The results are based on a data sample corresponding to an integrated luminosity of 19.7 fb-1 recorded with the CMS detector at the LHC. The cross section is measured inclusively, as well as separately for top (t) and antitop (t¯), in final states with a muon or an electron. The measured inclusive t-channel cross section is σ t-ch. = 83.6 ± 2.3 (stat.) ± 7.4 (syst.) pb. The single t and t¯ cross sections are measured to be σ t-ch.(t) =more » 53.8 ± 1.5 (stat.) ± 4.4 (syst.) pb and σ t-ch. (t¯) = 27.6 ± 1.3 (stat.) ± 3.7 (syst.) pb, respectively. The measured ratio of cross sections is R t-ch. = σ t-ch.(t)/σ t-ch. (t¯) = 1.95 ± 0.10 (stat.) ± 0.19 (syst.), in agreement with the standard model prediction. Finally, the modulus of the Cabibbo-Kobayashi-Maskawa matrix element V tb is extracted and, in combination with a previous CMS result at √s = 7 TeV, a value |V tb| = 0.998 ± 0.038 (exp.) ± 0.016 (theo.) is obtained.« less

  8. Stereochemical conversion of C3-vinyl group to 1-hydroxyethyl group in bacteriochlorophyll c by the hydratases BchF and BchV: adaptation of green sulfur bacteria to limited-light environments.

    PubMed

    Harada, Jiro; Teramura, Misato; Mizoguchi, Tadashi; Tsukatani, Yusuke; Yamamoto, Ken; Tamiaki, Hitoshi

    2015-12-01

    Photosynthetic green sulfur bacteria inhabit anaerobic environments with very low-light conditions. To adapt to such environments, these bacteria have evolved efficient light-harvesting antenna complexes called as chlorosomes, which comprise self-aggregated bacteriochlorophyll c in the model green sulfur, bacterium Chlorobaculum tepidum. The pigment possess a hydroxy group at the C3(1) position that produces a chiral center with R- or S-stereochemistry and the C3(1) -hydroxy group serves as a connecting moiety for the self-aggregation. Chlorobaculum tepidum carries the two possible homologous genes for C3-vinyl hydratase, bchF and bchV. In the present study, we constructed deletion mutants of each of these genes. Pigment analyses of the bchF-inactivated mutant, which still has BchV as a sole hydratase, showed higher ratios of S-epimeric bacteriochlorophyll c than the wild-type strain. The heightened prevalence of S-stereoisomers in the mutant was more remarkable at lower light intensities and caused a red shift of the chlorosomal Qy absorption band leading to advantages for light-energy transfer. In contrast, the bchV-mutant possessing only BchF showed a significant decrease of the S-epimers and accumulations of C3-vinyl BChl c species. As trans- criptional level of bchV was upregulated at lower light intensity, the Chlorobaculum tepidum adapted to low-light environments by control of the bchV transcription.

  9. Measurement of L X-ray fluorescence cross-sections for elements with 45 ⩽ Z ⩽ 50 using synchrotron radiation at 8 keV

    NASA Astrophysics Data System (ADS)

    Bonzi, Edgardo V.; Badiger, Nagappa M.; Grad, Gabriela B.; Barrea, Raúl A.; Figueroa, Rodolfo G.

    2011-10-01

    The L shell fluorescence cross-sections of the elements in range 45 ⩽ Z ⩽ 50 have been determined at 8 keV using Synchrotron radiation. The individual L X-ray photons, Ll, Lα, LβI, LβII, LγI and LγII produced in the target were measured with high resolution Si( Li) detector. The experimental set-up provided a low background by using linearly polarized monoenergetic photon beam, improving the signal-to-noise ratio. The experimental cross-sections obtained in this work were compared with available experimental data from Scofield [1,2] Krause [3,4] and Scofield and Puri et al. [5,6]. These experimental values closely agree with the theoretical values calculated using Scofield and Krause data, except for the case of Lγ, where values measured of this work are slighter higher.

  10. Ages and sources of components of Zn-Pb, Cu, precious metal, and platinum group element deposits in the goodsprings district, clark county, Nevada

    USGS Publications Warehouse

    Vikre, P.; Browne, Q.J.; Fleck, R.; Hofstra, A.; Wooden, J.

    2011-01-01

    The Goodsprings district, Clark County, Nevada, includes zinc-dominant carbonate replacement deposits of probable late Paleozoic age, and lead-dominant carbonate replacement deposits, copper ?? precious metal-platinum group element (PGE) deposits, and gold ?? silver deposits that are spatially associated with Late Triassic porphyritic intrusions. The district encompasses ??500 km2 although the distribution of all deposits has been laterally condensed by late Mesozoic crustal contraction. Zinc, Pb, and Cu production from about 90 deposits was ??160,000 metric tons (t) (Zn > Pb >> Cu), 2.1 million ounces (Moz) Ag, 0.09 Moz Au, and small amounts of PGEs-Co, V, Hg, Sb, Ni, Mo, Mn, Ir, and U-were also recovered. Zinc-dominant carbonate replacement deposits (Zn > Pb; Ag ?? Cu) resemble Mississippi Valley Type (MVT) Zn-Pb deposits in that they occur in karst and fault breccias in Mississippian limestone where the southern margin of the regional late Paleozoic foreland basin adjoins Proterozoic crystalline rocks of the craton. They consist of calcite, dolomite, sphalerite, and galena with variably positive S isotope compositions (??34S values range from 2.5-13%), and highly radiogenic Pb isotope compositions (206Pb/204Pb >19), typical of MVT deposits above crystalline Precambrian basement. These deposits may have formed when southward flow of saline fluids, derived from basinal and older sedimentary rocks, encountered thinner strata and pinch-outs against the craton, forcing fluid mixing and mineral precipitation in karst and fault breccias. Lead-dominant carbonate replacement deposits (Pb > Zn, Ag ?? Cu ?? Au) occur among other deposit types, often near porphyritic intrusions. They generally contain higher concentrations of precious metals than zinc-dominant deposits and relatively abundant iron oxides after pyrite. They share characteristics with copper ?? precious metal- PGE and gold ?? silver deposits including fine-grained quartz replacement of carbonate minerals in

  11. Group V secreted phospholipase A2 is upregulated by IL-4 in human macrophages and mediates phagocytosis via hydrolysis of ethanolamine phospholipids.

    PubMed

    Rubio, Julio M; Rodríguez, Juan P; Gil-de-Gómez, Luis; Guijas, Carlos; Balboa, María A; Balsinde, Jesús

    2015-04-01

    Studies on the heterogeneity and plasticity of macrophage populations led to the identification of two major polarization states: classically activated macrophages or M1, induced by IFN-γ plus LPS, and alternatively activated macrophages, induced by IL-4. We studied the expression of multiple phospholipase A2 enzymes in human macrophages and the effect that polarization of the cells has on their levels. At least 11 phospholipase A2 genes were found at significant levels in human macrophages, as detected by quantitative PCR. None of these exhibited marked changes after treating the cells with IFN-γ plus LPS. However, macrophage treatment with IL-4 led to strong upregulation of the secreted group V phospholipase A2 (sPLA2-V), both at the mRNA and protein levels. In parallel with increasing sPLA2-V expression levels, IL-4-treated macrophages exhibited increased phagocytosis of yeast-derived zymosan and bacteria, and we show that both events are causally related, because cells deficient in sPLA2-V exhibited decreased phagocytosis, and cells overexpressing the enzyme manifested higher rates of phagocytosis. Mass spectrometry analyses of lipid changes in the IL-4-treated macrophages suggest that ethanolamine lysophospholipid (LPE) is an sPLA2-V-derived product that may be involved in regulating phagocytosis. Cellular levels of LPE are selectively maintained by sPLA2-V. By supplementing sPLA2-V-deficient cells with LPE, phagocytosis of zymosan or bacteria was fully restored in IL-4-treated cells. Collectively, our results show that sPLA2-V is required for efficient phagocytosis by IL-4-treated human macrophages and provide evidence that sPLA2-V-derived LPE is involved in the process.

  12. The Supreme Court Permits Religious Groups To Use Public School Facilities: Good News Club v. Milford Central School.

    ERIC Educational Resources Information Center

    Russo, Charles J.; Mawdsley, Ralph D.

    2001-01-01

    Reviews basis for U.S. Supreme Court's June 2001 decision in "Good News Club v. Milford Central School," where Court held that the Christian religious club for students had the Constitutional right under the Free Speech Clause to use public school facilities after school hours. Explains impact of decision on board of education policy.…

  13. Evaluation of cross sections for Lα x-ray production by up to 4 MeV protons in representative elements from silver to uranium

    NASA Astrophysics Data System (ADS)

    Lapicki, Gregory

    2009-07-01

    Over the last two decades, Lα x-ray production cross sections have been fitted with a number of empirical formulae. Cross sections obtained from these formulae are averaged and fitted to a new empirical formula. These new empirical cross sections are compared with the results of the plane-wave Born approximation and the ECPSSR theory of Brandt and Lapicki (1981 Phys. Rev. A 23 1717). They are also gauged by the ECPSSR theory that has been corrected with a united atom approach in slow collisions, evaluated with Dirac-Hartree-Slater instead of screened hydrogenic wavefunctions, modified for intra-shell couplings as well as the change of the atomic parameters due to multiple ionizations. The effects of appropriately normalized intra-shell coupling factors and of multiple ionization were found to be small and essentially offset each other. The role of different sets of atomic parameters in conversion of the predictions of these ionization theories for Lα x-ray production in elements from the 47 <= Z2 <= 92 range of target atoms bombarded by up to 4 MeV protons is examined, and the selection of the optimal combination of ionization theory and atomic parameters for a reliable data base for PIXE analysis of elements heavier than palladium is discussed.

  14. G2(+)M study on N-alkylamino cation affinities of neutral main-group element hydrides: trends across the periodic table.

    PubMed

    Geng, Song; Wu, Ding-Lu; Yang, Jing; Wei, Xi-Guang; Zhu, Jun; Zhang, Hai-Bo; Ren, Yi; Lau, Kai-Chung

    2014-05-08

    We have made an extensive theoretical exploration of gas-phase N-alkylamino cation affinities (NAAMCA), including amino cation affinities (AMCA) and N-dimethylamino cation affinities (NDMAMCA), of neutral main-group element hydrides of groups 15-17 and periods 2-4 in the periodic table by using the G2(+)M method. Some similarities and differences are found between NAAMCA and the corresponding alkyl cation affinities (ACA) of H(n)X. Our calculations show that the AMCA and NDMAMCA are systematically lower than the corresponding proton affinities (PA) for H(n)X. In general, there is no linear correlation between NAAMCA and PA of H(n)X. Instead, the correlations exist only within the central elements X in period 2, or periods 3-4, which is significantly different from the reasonable correlations between ACA and PA for all H(n)X. NAAMCA (H(n)X) are weaker than NAAMCA (H(n-1)X(-)) by more than 700 kJ/mol and generally stronger than ACA (H(n)X), with three exceptions: H2ONR2(+)(R = H, Me) and HFNH2(+). These new findings can be rationalized by the negative hyperconjugation and Pauli repulsion.

  15. Systematics of Platinum-Group Element Distribution in the Boninitic Thetford Mines Ophiolite Complex, Canada: Melting and Fractional Crystallization Effects

    NASA Astrophysics Data System (ADS)

    Page, P.; Bedard, J.; Tremblay, A.; Minarik, W.

    2004-05-01

    and chromite from the boninitic parent melt. Economic concentrations of PGE have been observed in intracrustal discordant chromitite (up to 20g/t) bodies in the Pyroxenitic Zone as well as in some pyroxenite (> 500 ppb) without visible mineralization. The diversity of the platinum group minerals involve Hg, S and As, and the different parageneses suggest that the PGE-rich fluids are either magmatic (e.g. Hall deposit) or deuteric (e.g. StarChrome deposit). The Pt-Pd enriched intracrustal discordant chromitites are slightly enriched (2%) in radiogenic 187Os, hinting at the involvement of crustal sources in their genesis, either as basement to the arc or a flux from subducted crust. The Pt-186Os system rules out large amounts of Os transport from subducted crust.

  16. ICEG2D (v2.0) - An Integrated Software Package for Automated Prediction of Flow Fields for Single-Element Airfoils With Ice Accretion

    NASA Technical Reports Server (NTRS)

    Thompson David S.; Soni, Bharat K.

    2001-01-01

    An integrated geometry/grid/simulation software package, ICEG2D, is being developed to automate computational fluid dynamics (CFD) simulations for single- and multi-element airfoils with ice accretions. The current version, ICEG213 (v2.0), was designed to automatically perform four primary functions: (1) generate a grid-ready surface definition based on the geometrical characteristics of the iced airfoil surface, (2) generate high-quality structured and generalized grids starting from a defined surface definition, (3) generate the input and restart files needed to run the structured grid CFD solver NPARC or the generalized grid CFD solver HYBFL2D, and (4) using the flow solutions, generate solution-adaptive grids. ICEG2D (v2.0) can be operated in either a batch mode using a script file or in an interactive mode by entering directives from a command line within a Unix shell. This report summarizes activities completed in the first two years of a three-year research and development program to address automation issues related to CFD simulations for airfoils with ice accretions. As well as describing the technology employed in the software, this document serves as a users manual providing installation and operating instructions. An evaluation of the software is also presented.

  17. The origin and distribution of HAPs elements in relation to maceral composition of the A1 lignite bed (Paleocene, Calvert Bluff Formation, Wilcox Group), Calvert mine area, east-central Texas

    USGS Publications Warehouse

    Crowley, S.S.; Warwick, P.D.; Ruppert, L.F.; Pontolillo, J.

    1997-01-01

    The origin and distribution of twelve potentially Hazardous Air Pollutants (HAPs; As, Be, Cd, Cr, Co, Hg, Mn, Ni, Pb Sb, Se, and U) identified in the 1990 Clean Air Act Amendments were examined in relation to the maceral composition of the A1 bed (Paleocene, Calvert Bluff Formation, Wilcox Group) of the Calvert mine in east-central Texas. The 3.2 m-thick A1 bed was divided into nine incremental channel samples (7 lignite samples and 2 shaley coal samples) on the basis of megascopic characteristics. Results indicate that As, Cd, Cr, Ni, Pb, Sb, and U are strongly correlated with ash yield and are enriched in the shaley coal samples. We infer that these elements are associated with inorganic constituents in the coal bed and may be derived from a penecontemporaneous stream channel located several kilometers southeast of the mining block. Of the HAPs elements studied, Mn and Hg are the most poorly correlated to ash yield. We infer an organic association for Mn; Hg may be associated with pyrite. The rest of the trace elements (Be, Co, and Se) are weakly correlated with ash yield. Further analytical work is necessary to determine the mode of occurrence for these elements. Overall, concentrations of the HAPs elements are generally similar to or less than those reported in previous studies of lignites of the Wilcox Group, east-central region, Texas. Petrographic analysis indicates the following ranges in composition for the seven lignite samples: liptinites (5-8%), huminites (88-95%), and inertinites (trace amounts to 7%). Samples from the middle portion of the A1 bed contain abundant crypto-eugelinite compared to the rest of the samples; this relationship suggests that the degradation of plant material was an important process during the development of the peat mire. With the exception of Hg and Mn, relatively low levels of the HAPs elements studied are found in the samples containing abundant crypto-eugelinite. We infer that the peat-forming environment for this portion

  18. Practical routes to (SiH₃)₃P: applications in group IV semiconductor activation and in group III-V molecular synthesis.

    PubMed

    Tice, Jesse B; Chizmeshya, A V G; Tolle, J; D' Costa, V R; Menendez, J; Kouvetakis, J

    2010-05-21

    The (SiH₃)₃P hydride is introduced as a practical source for n-doping of group IV semiconductors and as a highly-reactive delivery agent of -(SiH₃)₂P functionalities in exploratory synthesis. In contrast to earlier methods, the compound is produced here in high purity quantitative yields via a new single-step method based on reactions of SiH₃Br and (Me₃Sn)₃P, circumventing the need for toxic and unstable starting materials. As an initial demonstration of its utility we synthesized monosubstituted Me₂M-P(SiH₃)₂ (M = Al, Ga, In) derivatives of Me₃M containing the (SiH₃)₂P ligand for the first time, in analogy to the known Me₂M-P(SiMe₃)₂ counterparts. A dimeric structure of Me₂M-P(SiH₃)₂ is proposed on the basis of spectroscopic characterizations and quantum chemical simulations. Next, in the context of materials synthesis, the (SiH₃)₃P compound was used to dope germanium for the first time by building a prototype p(++)Si(100)/i-Ge/n-Ge photodiode structure. The resultant n-type Ge layers contained active carrier concentrations of 3-4 × 10¹⁹ atoms cm⁻³ as determined by spectroscopic ellipsometry and confirmed by SIMS. Strain analysis using high resolution XRD yielded a Si content of 4 × 10²⁰ atoms cm⁻³ in agreement with SIMS and within the range expected for incorporating Si₃P type units into the diamond cubic Ge matrix. Extensive characterizations for structure, morphology and crystallinity indicate that the Si co-dopant plays essentially a passive role and does not compromise the device quality of the host material nor does it fundamentally alter its optical properties.

  19. Preparation, characterization, and theoretical analysis of group 14 element(I) dimers: a case study of magnesium(I) compounds as reducing agents in inorganic synthesis.

    PubMed

    Jones, Cameron; Bonyhady, Simon J; Holzmann, Nicole; Frenking, Gernot; Stasch, Andreas

    2011-12-19

    A synthetic route to the new amidine (DipNH)(DipN)C(C(6)H(4)Bu(t)-4) (ButisoH; Dip = C(6)H(3)Pr(i)(2)-2,6) has been developed. Its deprotonation with either LiBu(n) or KN(SiMe(3))(2) yields the amidinate complexes [M(Butiso)] (M = Li or K). Their reactions with group 14 element halides/pseudohalides afford the heteroleptic group 14 complexes [(Butiso)SiCl(3)], [(Butiso)ECl] (E = Ge or Sn), and [{(Butiso)Pb(μ-O(3)SCF(3))(THF)}(∞)], all of which have been crystallographically characterized. In addition, the synthesis and spectroscopic characterization of the homoleptic complex [Pb(Butiso)(2)] is reported. Reductions of the heteroleptic complexes with a soluble magnesium(I) dimer, [{((Mes)Nacnac)Mg}(2)] ((Mes)Nacnac = [(MesNCMe)(2)CH](-); Mes = mesityl), have given moderate-to-high yields of the group 14 element(I) dimers [{(Butiso)E}(2)] (E = Si, Ge, or Sn), the X-ray crystallographic studies of which reveal trans-bent structures. The corresponding lead(I) complex could not be prepared. Comprehensive spectroscopic and theoretical analyses of [{(Butiso)E}(2)] have allowed their properties to be compared. All complexes possess E-E single bonds and can be considered as intramolecularly base-stabilized examples of ditetrelynes, REER. Taken as a whole, this study highlights the synthetic utility of soluble and easy to prepare magnesium(I) dimers as valuable alternatives to the harsh, and often insoluble, alkali-metal reducing agents that are currently widely employed in the synthesis of low-oxidation-state organometallic/inorganic complexes.

  20. Generation of the V4.2m5 and AMPX and MPACT 51 and 252-Group Libraries with ENDF/B-VII.0 and VII.1

    SciTech Connect

    Kim, Kang Seog

    2016-12-12

    The evaluated nuclear data file (ENDF)/B-7.0 v4.1m3 MPACT 47-group library has been used as a main library for the Consortium for Advanced Simulation of Light Water Reactors (CASL) neutronics simulator in simulating pressurized water reactor (PWR) problems. Recent analysis for the high void boiling water reactor (BWR) fuels and burnt fuels indicates that the 47-group library introduces relatively large reactivity bias. Since the 47- group structure does not match with the SCALE 6.2 252-group boundaries, the CASL Virtual Environment for Reactor Applications Core Simulator (VERA-CS) MPACT library must be maintained independently, which causes quality assurance concerns. In order to address this issue, a new 51-group structure has been proposed based on the MPACT 47- g and SCALE 252-g structures. In addition, the new CASL library will include a 19-group structure for gamma production and interaction cross section data based on the SCALE 19- group structure. New AMPX and MPACT 51-group libraries have been developed with the ENDF/B-7.0 and 7.1 evaluated nuclear data. The 19-group gamma data also have been generated for future use, but they are only available on the AMPX 51-g library. In addition, ENDF/B-7.0 and 7.1 MPACT 252-g libraries have been generated for verification purposes. Various benchmark calculations have been performed to verify and validate the newly developed libraries.

  1. Platinum-group element, Gold, Silver and Base Metal distribution in compositionally zoned sulfide droplets from the Medvezky Creek Mine, Noril'sk, Russia

    USGS Publications Warehouse

    Barnes, S.-J.; Cox, R.A.; Zientek, M.L.

    2006-01-01

    Concentrations of Ag, Au, Cd, Co, Re, Zn and Platinum-group elements (PGE) have been determined in sulfide minerals from zoned sulfide droplets of the Noril'sk 1 Medvezky Creek Mine. The aims of the study were; to establish whether these elements are located in the major sulfide minerals (pentlandite, pyrrhotite, chalcopyrite and cubanite), to establish whether the elements show a preference for a particular sulfide mineral and to investigate the model, which suggests that the zonation in the droplets is caused by the crystal fractionation of monosulfide solid solution (mss). Nickel, Cu, Ag, Re, Os, Ir, Ru, Rh and Pd, were found to be largely located in the major sulfide minerals. In contrast, less than 25% of the Au, Cd, Pt and Zn in the rock was found to be present in these sulfides. Osmium, Ir, Ru, Rh and Re were found to be concentrated in pyrrhotite and pentlandite. Palladium and Co was found to be concentrated in pentlandite. Silver, Cd and Zn concentrations are highest in chalcopyrite and cubanite. Gold and platinum showed no preference for any of the major sulfide minerals. The enrichment of Os, Ir, Ru, Rh and Re in pyrrhotite and pentlandite (exsolution products of mss) and the low levels of these elements in the cubanite and chalcopyrite (exsolution products of intermediate solid solution, iss) support the mss crystal fractionation model, because Os, Ir, Ru, Rh and Re are compatible with mss. The enrichment of Ag, Cd and Zn in chalcopyrite and cubanite also supports the mss fractionation model these minerals are derived from the fractionated liquid and these elements are incompatible with mss and thus should be enriched in the fractionated liquid. Gold and Pt do not partition into either iss or mss and become sufficiently enriched in the final fractionated liquid to crystallize among the iss and mss grains as tellurides, bismithides and alloys. During pentlandite exsolution Pd appears to have diffused from the Cu-rich portion of the droplet into

  2. Annual Hazard Rates of Recurrence for Breast Cancer During 24 Years of Follow-Up: Results From the International Breast Cancer Study Group Trials I to V

    PubMed Central

    Sun, Zhuoxin; Price, Karen N.; Karlsson, Per; Forbes, John F.; Thürlimann, Beat; Gianni, Lorenzo; Castiglione, Monica; Gelber, Richard D.; Coates, Alan S.; Goldhirsch, Aron

    2016-01-01

    Purpose Predicting the pattern of recurrence can aid in the development of targeted surveillance and treatment strategies. We identified patient populations that remain at risk for an event at a median follow-up of 24 years from the diagnosis of operable breast cancer. Patients and Methods International Breast Cancer Study Group clinical trials I to V randomly assigned 4,105 patients between 1978 and 1985. Annualized hazards were estimated for breast cancer–free interval (primary end point), disease-free survival, and overall survival. Results For the entire group, the annualized hazard of recurrence was highest during the first 5 years (10.4%), with a peak between years 1 and 2 (15.2%). During the first 5 years, patients with estrogen receptor (ER) – positive disease had a lower annualized hazard compared with those with ER-negative disease (9.9% v 11.5%; P = .01). However, beyond 5 years, patients with ER-positive disease had higher hazards (5 to 10 years: 5.4% v 3.3%; 10 to 15 years: 2.9% v 1.3%; 15 to 20 years: 2.8% v 1.2%; and 20 to 25 years: 1.3% v 1.4%; P < .001). Among patients with ER-positive disease, annualized hazards of recurrence remained elevated and fairly stable beyond 10 years, even for those with no axillary involvement (2.0%, 2.1%, and 1.1% for years 10 to 15, 15 to 20, and 20 to 25, respectively) and for those with one to three positive nodes (3.0%, 3.5%, and 1.5%, respectively). Conclusion Patients with ER-positive breast cancer maintain a significant recurrence rate during extended follow up. Strategies for follow up and treatments to prevent recurrences may be most efficiently applied and studied in patients with ER-positive disease followed for a long period of time. PMID:26786933

  3. Group benefit and protection of pediatric research subjects: Grimes v. Kennedy Krieger and the Lead Abatement Study.

    PubMed

    Kopelman, Loretta M

    2002-01-01

    The Maryland Court of Appeals in Grimes v. Kennedy Krieger Institute was sharply critical of the lead abatement study conducted by this Institute, an affiliate of Johns Hopkins University. Grimes ruled that investigators might, given the facts of the case, have a special relationship with subjects, thereby creating a duty of care that could, if breached, give rise to an action in negligence. This ruling has implications for pediatric research practices and long-standing disputes among informed people of good will about what pediatric studies should be permitted.

  4. Ion-selective electrode in determining fluorine in binary fluorides of metals of groups II-V

    SciTech Connect

    Mishchenko, V.T.; Mukomel', V.L.; Polvektov, N.S.; Shilova, L.P.; Tselik, E.I.

    1986-01-01

    The authors have developed a method of determining fluorine by ion-selective electrode techniques in specimens containing mixtures of the fluorides of magnesium and the rare-earth elements (REE), as well as scandium and bismuth. The specimens after treatment at high temperatures are sparingly soluble at room temperature in water and also in aqueous solutions of acids and bases. The authors found that a mixture of KNaCO/sub 3/ and K/sub 2/S/sub 2/O/sub 8/ with a mass ratio of 2:1 was an effective flux for MgF/sub 2/-MeF/sub 3/ specimens, where Me is an REE ion. The combined method of analyzing binary mixtures of fluorides (Mg and REE, Sc and Bi) which provides satisfactory accuracy and reliability in determining the fluoride and two different metals whose compounds may have various ratios in the samples.

  5. LBRIG Newsletter: The Trimestrial Publication of the Language by Radio Interest Group, Vol. V, No.1, September, 1976.

    ERIC Educational Resources Information Center

    Garfinkel, Alan, Ed.; And Others

    This issue of the Language by Radio Interest Group newsletter contains: an article by Paul A. Gaeng on his experience as a radio listener, an article by Richard E. Wood on "Radio Peking," and a partial reprint of frequency listings from the January 1976 number. Gaeng reports that, when he was a student in Geneva, he developed skills as a…

  6. 75 FR 11681 - United States v. Daily Gazette Company and Medianews Group, Inc.; Proposed Final Judgment and...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-03-11

    ... Newspapers Holdings Limited Partnership, Gazette Company owns all the assets and controls all the business... ownership and control of the only two daily newspapers in Charleston, West Virginia under the Daily Gazette...News Group with governance rights and independent control over the editorial operations of...

  7. HRTEM-AEM-HAADF-STEM study of platinum-group elements within a mantle-derived Cr spinel (Lherz; North-Eastern Pyrenees, France)

    NASA Astrophysics Data System (ADS)

    Ferraris, Cristiano; Lorand, Jean-Pierre

    2008-11-01

    As platinum group elements (PGE) like Ru, Os, Ir and Rh have appropriate charge and ionic radii to substitute the major cations in the spinel structure, Cr-spinel is one of the potential minerals that can fractionate such elements during the partial melting and fractional crystallization. However, whether PGE occur in solid solution or are physically collected as poly-metallic clusters of atoms on spinel grain boundaries is a central issue for PGE geochemistry. A PGE-bearing Cr-spinel separated from one harzburgite sample from Lherz has been analyzed by Transmission, Analytical and Scanning-Transmission Electron Microscopy (TEM-AEM-STEM). Our analyses did not reveal any exsolution/cluster feature at the nanometric scale, except for Ir, which is concentrated as Ir-bearing lamellar rutile, about 100 nm width. Rutile appears to have enhanced unmixing of Ir from the spinel structure. The DCr spinel/silicate melt partition coefficients estimated from the Lherz Cr-spinel (Ir = 32 ± 0.7; Os = 28 ± 6; Ru = 12.5 ± 2; Pt = 1.5 ± 0.2; Pd = 0.2 ± 0.05) may be appropriate for modelling the behavior of PGE in sulfur-undersaturated melting processes of the shallow upper mantle, while being lower than those derived from experiments and natural ultramafic melts.

  8. Correlation consistent basis sets for explicitly correlated wavefunctions: pseudopotential-based basis sets for the post-d main group elements Ga-Rn.

    PubMed

    Hill, J Grant; Peterson, Kirk A

    2014-09-07

    New correlation consistent basis sets, cc-pVnZ-PP-F12 (n = D, T, Q), for all the post-d main group elements Ga-Rn have been optimized for use in explicitly correlated F12 calculations. The new sets, which include not only orbital basis sets but also the matching auxiliary sets required for density fitting both conventional and F12 integrals, are designed for correlation of valence sp, as well as the outer-core d electrons. The basis sets are constructed for use with the previously published small-core relativistic pseudopotentials of the Stuttgart-Cologne variety. Benchmark explicitly correlated coupled-cluster singles and doubles with perturbative triples [CCSD(T)-F12b] calculations of the spectroscopic properties of numerous diatomic molecules involving 4p, 5p, and 6p elements have been carried out and compared to the analogous conventional CCSD(T) results. In general the F12 results obtained with a n-zeta F12 basis set were comparable to conventional aug-cc-pVxZ-PP or aug-cc-pwCVxZ-PP basis set calculations obtained with x = n + 1 or even x = n + 2. The new sets used in CCSD(T)-F12b calculations are particularly efficient at accurately recovering the large correlation effects of the outer-core d electrons.

  9. Multireference - Møller-Plesset Perturbation Theory Results on Levels and Transition Rates in Al-like Ions of Iron Group Elements

    SciTech Connect

    Santana, J A; Ishikawa, Y; Tr�abert, E

    2009-02-26

    Ground configuration and low-lying levels of Al-like ions contribute to a variety of laboratory and solar spectra, but the available information in databases are neither complete not necessarily correct. We have performed multireference Moeller-Plesset perturbation theory calculations that approach spectroscopic accuracy in order to check the information that databases hold on the 40 lowest levels of Al-Like ions of iron group elements (K through Ge), and to provide input for the interpretation of concurrent experiments. Our results indicate problems of the database holdings on the levels of the lowest quartet levels in the lighter elements of the range studied. The results of our calculations of the decay rates of five long-lived levels (3s{sup 2}3p {sup 2}p{sup o}{sub 3/2}, 3s3p{sup 2} {sup 4}P{sup o} J and 3s3p3d {sup 4}F{sup o}{sub 9/2}) are compared with lifetime data from beam-foil, electron beam ion trap and heavy-ion storage ring experiments.

  10. Ir, Ru, Pt, and Pd in basalts and komatiites: New constraints for the geochemical behavior of the platinum-group elements in the mantle

    SciTech Connect

    Rehkaemper, M.; Halliday, A.N.; Fitton, J.G.; Lee, D.C.; Wieneke, M.; Arndt, N.T.

    1999-11-01

    The concentrations of the platinum-group elements (PGE) Ir, Ru, Pt, and Pd were determined in 18 mantle-derived basalts from a variety of tectonic settings and six komatiites from three locations. All analyses were performed using isotope dilution, Carius tube digestion, and the precise technique of multiple collector inductively coupled plasma mass spectrometry. Multiple analyses of two samples indicate external reproducibilities, based upon separate dissolutions, or approximately 2--9% in the ppt to ppb concentration range. Mid-ocean ridge basalts from the Kolbeinsey Ridge, tholeiites from Iceland and alkali basalts from the Cameroon Line define three individual samples suites that are characterized by distinct major, trace, and platinum-group element systematics. All three-sample suites display correlations of the PGE with MgO, Ni, and Cr. The new analytical results are employed to constrain the geochemical behavior of the PGE during the formation and differentiation of mantle-derived melts. The PGE are inferred to be compatible in sulfides during partial melting with sulfide-silicate melt partition coefficients of {approximately}1 x 10{sup 4}. The fractionated PGE patterns of mantle melts re a consequence of the incompatibility of Pd in nonsulfide phases, whereas Ir and Ru must be compatible in at least one other mantle phase. Model calculations indicate that PGE alloys or spinel may be responsible for the higher compatibility of the latter elements during partial melting. It is further demonstrated that the shape of the melting regime has a profound effect on the PGE systematics of mantle magmas. The systematic trends of the three samples suites in plots of PGE against Ni and Cr are the results of magma differentiation processes that involve fractional crystallization of silicate minerals and the concurrent segregation of an immiscible sulfide liquid. The behavior of the PGE during magma fractionation indicates that the segregated sulfides probably equilibrate

  11. Platinum-group element signatures in the North Atlantic Igneous Province: Implications for mantle controls on metal budgets during continental breakup

    NASA Astrophysics Data System (ADS)

    Hughes, Hannah S. R.; McDonald, Iain; Kerr, Andrew C.

    2015-09-01

    The North Atlantic Igneous Province (NAIP) is a large igneous province (LIP) that includes a series of lava suites erupted from the earliest manifestations of the (proto)-Icelandic plume, through continental rifting and ultimate ocean opening. The lavas of one of these sub-provinces, the British Palaeogene Igneous Province (BPIP), were some of the first lavas to be erupted in the NAIP and overlie a thick crustal basement and sedimentary succession with abundant S-rich mudrocks. We present the first platinum-group element (PGE) and Au analyses of BPIP flood basalts from the main lava fields of the Isle of Mull and Morvern and the Isle of Skye, in addition to a suite of shallow crustal dolerite volcanic plugs on Mull, and other minor lavas suites. BPIP lavas display both S-saturated and S-undersaturated trends which, coupled with elevated PGE abundances (> MORB), suggest that the BPIP is one of the most prospective areas of the NAIP to host Ni-Cu-PGE-(Au) mineralisation in conduit systems. Platinum-group element, Au and chalcophile element abundances in lavas from West and East Greenland, and Iceland, are directly comparable to BPIP lavas, but the relative abundances of Pt and Pd vary systematically between lavas suites of different ages. The oldest lavas (BPIP and West Greenland) have a broadly chondritic Pt/Pd ratio ( 1.9). Lavas from East Greenland have a lower Pt/Pd ratio ( 0.8) and the youngest lavas from Iceland have the lowest Pt/Pd ratio of the NAIP ( 0.4). Hence, Pt/Pd ratio of otherwise equivalent flood basalt lavas varies temporally across the NAIP and appears to be coincident with the changing geodynamic environment of the (proto)-Icelandic plume through time. We assess the possible causes for such systematic Pt/Pd variation in light of mantle plume and lithospheric controls, and suggest that this reflects a change in the availability of lithospheric mantle Pt-rich sulphides for entrainment in ascending plume magmas. Hence the precious metal systematics

  12. “Structural Transformations in Ceramics: Perovskite-like Oxides and Group III, IV, and V Nitrides”

    SciTech Connect

    James P. Lewis , Dorian M. Hatch , and Harold T. Stokes

    2006-12-31

    1 Overview of Results and their Significance Ceramic perovskite-like oxides with the general formula (A. A0. ...)(B. B0. ...)O3and titanium-based oxides are of great technological interest because of their large piezoelectric and dielectric response characteristics.[1] In doped and nanoengineered forms, titantium dioxide finds increasing application as an organic and hydrolytic photocatalyst. The binary main-group-metal nitride compounds have undergone recent advancements of in-situ heating technology in diamond anvil cells leading to a burst of experimental and theoretical interest. In our DOE proposal, we discussed our unique theoretical approach which applies ab initio electronic calculations in conjunction with systematic group-theoretical analysis of lattice distortions to study two representative phase transitions in ceramic materials: (1) displacive phase transitions in primarily titanium-based perovskite-like oxide ceramics, and (2) reconstructive phase transitions in main-group nitride ceramics. A sub area which we have explored in depth is doped titanium dioxide electrical/optical properties.

  13. Design, synthesis and 1H NMR study of C3v-symmetric anion receptors with urethane-NH as recognition group

    NASA Astrophysics Data System (ADS)

    Park, Jin-Oh; Sahoo, Suban K.; Choi, Heung-Jin

    2016-01-01

    C3v-Symmetric anion receptors 3 and 4 with urethane groups were synthesized by using trindane triol as tripodal molecular framework. In 1H NMR titration study, the receptors showed noticeable downfield shift/disappearance of the urethane-NH peak in presence of H2PO4- and F- due to the host-guest complexation occurred through multiple hydrogen bonding and/or the deprotonation of urethane-NH groups. Other tested anions such as Cl-, Br-, HSO4-, and NO3- showed either no or negligible chemical shift of the urethane groups. The deprotonation event in 4 allowed selective detection of F- by perceptible color change from colorless to yellowish-red with the appearance of a new charge transfer absorption band at 450 nm.

  14. Ectomycorrhizal Influence on Particle Size, Surface Structure, Mineral Crystallinity, Functional Groups, and Elemental Composition of Soil Colloids from Different Soil Origins

    PubMed Central

    Li, Yanhong; Wang, Huimei; Wang, Wenjie; Yang, Lei; Zu, Yuangang

    2013-01-01

    Limited data are available on the ectomycorrhizae-induced changes in surface structure and composition of soil colloids, the most active portion in soil matrix, although such data may benefit the understanding of mycorrhizal-aided soil improvements. By using ectomycorrhizae (Gomphidius viscidus) and soil colloids from dark brown forest soil (a good loam) and saline-alkali soil (heavily degraded soil), we tried to approach the changes here. For the good loam either from the surface or deep soils, the fungus treatment induced physical absorption of covering materials on colloid surface with nonsignificant increases in soil particle size (P > 0.05). These increased the amount of variable functional groups (O–H stretching and bending, C–H stretching, C=O stretching, etc.) by 3–26% and the crystallinity of variable soil minerals (kaolinite, hydromica, and quartz) by 40–300%. However, the fungus treatment of saline-alkali soil obviously differed from the dark brown forest soil. There were 12–35% decreases in most functional groups, 15–55% decreases in crystallinity of most soil minerals but general increases in their grain size, and significant increases in soil particle size (P < 0.05). These different responses sharply decreased element ratios (C : O, C : N, and C : Si) in soil colloids from saline-alkali soil, moving them close to those of the good loam of dark brown forest soil. PMID:23766704

  15. Ectomycorrhizal influence on particle size, surface structure, mineral crystallinity, functional groups, and elemental composition of soil colloids from different soil origins.

    PubMed

    Li, Yanhong; Wang, Huimei; Wang, Wenjie; Yang, Lei; Zu, Yuangang

    2013-01-01

    Limited data are available on the ectomycorrhizae-induced changes in surface structure and composition of soil colloids, the most active portion in soil matrix, although such data may benefit the understanding of mycorrhizal-aided soil improvements. By using ectomycorrhizae (Gomphidius viscidus) and soil colloids from dark brown forest soil (a good loam) and saline-alkali soil (heavily degraded soil), we tried to approach the changes here. For the good loam either from the surface or deep soils, the fungus treatment induced physical absorption of covering materials on colloid surface with nonsignificant increases in soil particle size (P > 0.05). These increased the amount of variable functional groups (O-H stretching and bending, C-H stretching, C=O stretching, etc.) by 3-26% and the crystallinity of variable soil minerals (kaolinite, hydromica, and quartz) by 40-300%. However, the fungus treatment of saline-alkali soil obviously differed from the dark brown forest soil. There were 12-35% decreases in most functional groups, 15-55% decreases in crystallinity of most soil minerals but general increases in their grain size, and significant increases in soil particle size (P < 0.05). These different responses sharply decreased element ratios (C:O, C:N, and C:Si) in soil colloids from saline-alkali soil, moving them close to those of the good loam of dark brown forest soil.

  16. Contrasting Behavior of the Z Bonds in X-Z···Y Weak Interactions: Z = Main Group Elements Versus the Transition Metals.

    PubMed

    Joy, Jyothish; Jemmis, Eluvathingal D

    2017-02-06

    In contrast to the increasing family of weak intermolecular interactions in main-group compounds (X-Z···Y, Z = main-group elements), an analysis of the Cambridge Structural Database indicates that electron-saturated (18-electron) transition-metal complexes show reluctance toward weak M bond formation (X-M···Y, M = transition metal). In particular, weak M bonds involving electron-saturated (18-electron) complexes of transition metals with partially filled d-orbitals are not found. We propose that the nature of valence electron density distribution in transition-metal complexes is the primary reason for this reluctance. A survey of the interaction of selected electron-saturated transition-metal complexes with electron-rich molecules (Y) demonstrates the following: shielding the possible σ-hole on the metal center by the core electron density in 3d series, and enhanced electronegativity and relativistic effects in 4d and 5d series, hinders the formation of the M bond. A balance in all the destabilizing effects has been found in the 4d series due to its moderate polarizability and primogenic repulsion from inner core d-electrons. A changeover in the donor-acceptor nature of the metal center toward different types of incoming molecules is also unveiled here. The present study confirms the possibility of M bond as a new supramolecular force in designing the crystal structures of electron-saturated transition-metal complexes by invoking extreme ligand conditions.

  17. Efficient and Accurate Identification of Platinum-Group Minerals by a Combination of Mineral Liberation and Electron Probe Microanalysis with a New Approach to the Offline Overlap Correction of Platinum-Group Element Concentrations.

    PubMed

    Osbahr, Inga; Krause, Joachim; Bachmann, Kai; Gutzmer, Jens

    2015-10-01

    Identification and accurate characterization of platinum-group minerals (PGMs) is usually a very cumbersome procedure due to their small grain size (typically below 10 µm) and inconspicuous appearance under reflected light. A novel strategy for finding PGMs and quantifying their composition was developed. It combines a mineral liberation analyzer (MLA), a point logging system, and electron probe microanalysis (EPMA). As a first step, the PGMs are identified using the MLA. Grains identified as PGMs are then marked and coordinates recorded and transferred to the EPMA. Case studies illustrate that the combination of MLA, point logging, and EPMA results in the identification of a significantly higher number of PGM grains than reflected light microscopy. Analysis of PGMs by EPMA requires considerable effort due to the often significant overlaps between the X-ray spectra of almost all platinum-group and associated elements. X-ray lines suitable for quantitative analysis need to be carefully selected. As peak overlaps cannot be avoided completely, an offline overlap correction based on weight proportions has been developed. Results obtained with the procedure proposed in this study attain acceptable totals and atomic proportions, indicating that the applied corrections are appropriate.

  18. Platinum-group element distribution in base-metal sulfides of the Merensky Reef from the eastern and western Bushveld Complex, South Africa

    NASA Astrophysics Data System (ADS)

    Osbahr, Inga; Klemd, Reiner; Oberthür, Thomas; Brätz, Helene; Schouwstra, Robert

    2013-02-01

    Base-metal sulfides in magmatic Ni-Cu-PGE deposits are important carriers of platinum-group elements (PGE). The distribution and concentrations of PGE in pentlandite, pyrrhotite, chalcopyrite, and pyrite were determined in samples from the mineralized portion of four Merensky Reef intersections from the eastern and western Bushveld Complex. Electron microprobe analysis was used for major elements, and in situ laser ablation inductively-coupled plasma mass spectrometry (LA-ICP-MS) for trace elements (PGE, Ag, and Au). Whole rock trace element analyses were performed on representative samples to obtain mineralogical balances. In Merensky Reef samples from the western Bushveld, both Pt and Pd are mainly concentrated in the upper chromitite stringer and its immediate vicinity. Samples from the eastern Bushveld reveal more complex distribution patterns. In situ LA-ICP-MS analyses of PGE in sulfides reveal that pentlandite carries distinctly elevated PGE contents, whereas pyrrhotite and chalcopyrite only contain very low PGE concentrations. Pentlandite is the principal host of Pd and Rh in the ores. Palladium and Rh concentrations in pentlandite reach up to 700 and 130 ppm, respectively, in the samples from the eastern Bushveld, and up to 1,750 ppm Pd and up to 1,000 ppm Rh in samples from the western Bushveld. Only traces of Pt are present in the base-metal sulfides (BMS). Pyrrhotite contains significant though generally low amounts of Ru, Os, and Ir, but hardly any Pd or Rh. Chalcopyrite contains most of the Ag but carries only extremely low PGE concentrations. Mass balance calculations performed on the Merensky Reef samples reveal that in general, pentlandite in the feldspathic pyroxenite and the pegmatoidal feldspathic pyroxenite hosts up to 100 % of the Pd and Rh and smaller amounts (10-40 %) of the Os, Ir, and Ru. Chalcopyrite and pyrrhotite usually contain less than 10 % of the whole rock PGE. The remaining PGE concentrations, and especially most of the Pt (up to

  19. Effects of mother lode-type gold mineralization on 187Os/188Os and platinum group element concentrations in peridotite: Alleghany District, California

    USGS Publications Warehouse

    Walker, R.J.; Böhlke, J.K.; McDonough, W.F.; Li, J.

    2007-01-01

    Osmium isotope compositions and concentrations of Re, platinum group elements (PGE), and Au were determined for host peridotites (serpentinites and barzburgites) and hydrothermally altered ultramafic wall rocks associated with Mother Lode-type hydrothermal gold-quartz vein mineralization in the Alleghany district, California. The host peridotites have Os isotope compositions and Re, PGE, and Au abundances typical of the upper mantle at their presumed formation age during the late Proterozoic or early Paleozoic. The hydrothermally altered rocks have highly variable initial Os isotope compositions with ??os, values (% deviation of 187OS/188OS from the chondritic average calculated for the approx. 120 Ma time of mineralization) ranging from -1.4 to -8.3. The lowest Os isotope compositions are consistent with Re depletion of a chondritic source (e.g., the upper mantle) at ca. 1.6 Ga. Most of the altered samples are enriched in Au and have depleted and fractionated abundances of Re and PGE relative to their precursor peridotites. Geoehemical characteristics of the altered samples suggest that Re and some PGE were variably removed from the ultramafic rocks during the mineralization event. In addition to Re, the Pt and Pd abundances of the most intensely altered rocks appear to have been most affected by mineralization. The 187Os-depleted isotopic compositions of some altered rocks are interpreted to be a result of preferential 187Os loss via destruction of Re-rich phases during the event. For these rocks, Os evidently is not a useful tracer of the mineralizing fluids. The results do, however, provide evidence for differential mobility of these elements, and mobility of 187Os relative to the initial bulk Os isotope composition during hydrothermal metasomatic alteration of ultramafic rocks. ?? 2007 Society of Economic Geologists, Inc.

  20. Epithelial Expression of Human ABO Blood Group Genes Is Dependent upon a Downstream Regulatory Element Functioning through an Epithelial Cell-specific Transcription Factor, Elf5.

    PubMed

    Sano, Rie; Nakajima, Tamiko; Takahashi, Yoichiro; Kubo, Rieko; Kobayashi, Momoko; Takahashi, Keiko; Takeshita, Haruo; Ogasawara, Kenichi; Kominato, Yoshihiko

    2016-10-21

    The human ABO blood group system is of great importance in blood transfusion and organ transplantation. The ABO system is composed of complex carbohydrate structures that are biosynthesized by A- and B-transferases encoded by the ABO gene. However, the mechanisms regulating ABO gene expression in epithelial cells remain obscure. On the basis of DNase I-hypersensitive sites in and around ABO in epithelial cells, we prepared reporter plasmid constructs including these sites. Subsequent luciferase assays and histone modifications indicated a novel positive regulatory element, designated the +22.6-kb site, downstream from ABO, and this was shown to enhance ABO promoter activity in an epithelial cell-specific manner. Expression of ABO and B-antigen was reduced in gastric cancer KATOIII cells by biallelic deletion of the +22.6-kb site using the CRISPR/Cas9 system. Electrophoretic mobility shift assay and chromatin immunoprecipitation assay demonstrated that the site bound to an epithelial cell-specific transcription factor, Elf5. Mutation of the Ets binding motifs to abrogate binding of this factor reduced the regulatory activity of the +22.6-kb site. Furthermore, ELF5 knockdown with shRNA reduced both endogenous transcription from ABO and B-antigen expression in KATOIII cells. Thus, Elf5 appeared to be involved in the enhancer potential of the +22.6-kb site. These results support the contention that ABO expression is dependent upon a downstream positive regulatory element functioning through a tissue-restricted transcription factor, Elf5, in epithelial cells.

  1. The Climate Hazards Group InfraRed Precipitation with Stations (CHIRPS) v2.0 Dataset: 35 year Quasi-Global Precipitation Estimates for Drought Monitoring

    NASA Astrophysics Data System (ADS)

    Peterson, P.; Funk, C. C.; Landsfeld, M. F.; Pedreros, D. H.; Shukla, S.; Husak, G. J.; Harrison, L.; Verdin, J. P.

    2015-12-01

    A high quality, long-term, high-resolution precipitation dataset is a key requirement for supporting drought monitoring and long term trend analysis. In this presentation we introduce a new dataset: the Climate Hazards group InfraRed Precipitation with Stations (CHIRPS) v2.0, developed by scientists at the University of California, Santa Barbara and the U.S. Geological Survey Earth Resources Observation and Science Center. This new quasi-global precipitation product is available at daily to seasonal time scales, with a spatial resolution of 0.05°, and a 1981 to near real-time period of record. The three main types of information used in the CHIRPS are: (1) global 0.05° precipitation climatologies, (2) gridded precipitation estimates derived from time-varying cold cloud duration, and (3) in situ precipitation observations. The Climate Hazards Group (CHG) has developed an extensive database of in situ daily, pentadal, and monthly precipitation totals with over a billion daily observations worldwide. A screening procedure was developed to flag and remove potential false zeros from the daily GTS and GSOD data. These potentially spurious data can artificially suppress CHIRPS rainfall totals. Using GPCC v7 as the best-available standard, we compare CHIRPS with ARC2, CFS-Reanalysis, CHIRP, CMORPH, CPC-Unified, ECMWF, PERSIANNE, RFE2, TAMSAT, TRMM-RT7, and TRMM-V7. The CHIRPS is shown to have higher correlation, and lower systematic errors (bias) and mean absolute errors with GPCC v7 than the other datasets. Comparison with independent validation data suggests that the CHIRPS performance is similar to research quality products like the GPCC and GPCP, but with higher resolution and lower latency. We conclude by looking at the change in availability of station data within a monitoring time frame, contrasting countries with and without near real time data.

  2. A Calibration Method for Group V Fluxes and Impact of V/III Flux Ratio on the Growth of InAs/InAsSb Type-II Superlattices by Molecular Beam Epitaxy

    DTIC Science & Technology

    2013-01-16

    x alloys and strain-balanced InAs/InAsxSb1?x superlattices on GaSb substrates by molecular beam epitaxy for IR optoelectronic device applications...Zhiyuan Lin, Zhao-Yu He, Qiang Zhang, Preston T. Webster, Shane R. Johnson , Lu Ouyang, David J. Smith, University of Illinois - Urbana Board of...calibration method for group V fluxes is demonstrated for the growth of InAsxSb1?x alloys and strain-balanced InAs/InAsxSb1?x superlattices on GaSb substrates

  3. Kaposi's sarcoma-associated herpesvirus (human herpesvirus 8) replication and transcription factor activates the K9 (vIRF) gene through two distinct cis elements by a non-DNA-binding mechanism.

    PubMed

    Ueda, Keiji; Ishikawa, Kayo; Nishimura, Ken; Sakakibara, Shuhei; Do, Eunju; Yamanishi, Koichi

    2002-12-01

    The replication and transcription activator (RTA) of Kaposi's sarcoma-associated herpesvirus (KSHV), or human herpesvirus 8, a homologue of Epstein-Barr virus BRLF1 or Rta, is a strong transactivator and inducer of lytic replication. RTA acting alone can induce lytic replication of KSHV in infected cell lines that originated from primary effusion lymphomas, leading to virus production. During the lytic replication process, RTA activates many kinds of genes, including polyadenylated nuclear RNA, K8, K9 (vIRF), ORF57, and so on. We focused here on the mechanism of how RTA upregulates the K9 (vIRF) promoter and identified two independent cis-acting elements in the K9 (vIRF) promoter that responded to RTA. These elements were finally confined to the sequence 5'-TCTGGGACAGTC-3' in responsive element (RE) I-2B and the sequence 5'-GTACTTAAAATA-3' in RE IIC-2, both of which did not share sequence homology. Multiple factors bound specifically with these elements, and their binding was correlated with the RTA-responsive activity. Electrophoretic mobility shift assay with nuclear extract from infected cells and the N-terminal part of RTA expressed in Escherichia coli, however, did not show that RTA interacted directly with these elements, in contrast to the RTA responsive elements in the PAN/K12 promoter region, the ORF57/K8 promoter region. Thus, it was likely that RTA could transactivate several kinds of unique cis elements without directly binding to the responsive elements, probably through cooperation with other DNA-binding factors.

  4. First principles DFT study of ferromagnetism in SnO{sub 2} induced by doped group 1A and 2A non-magnetic elements X (X=Li, Na, K, Be, Mg, Ca)

    SciTech Connect

    Chakraborty, Brahmananda Ramaniah, Lavanya M.

    2014-04-24

    Transition metal - free - ferromagnetism in diluted magnetic semiconductors (DMS) is of much current interest in the search for more efficient DMS materials for spintronic applications. Here, we report the results of our first principles density functional theory (DFT) study on impurity - induced ferromagnetism in non-magnetic SnO{sub 2} by a non-magnetic impurity. The impurities considered are sp-type of group 1A and 2A elements X (X = Li, Na, K, Be, Mg, Ca). Even a single atom of the group 1A elements makes the system magnetic, whereas for the group 2A elements Ca and Mg, a higher doping is required to induce ferromagnetism. For all the elements studied, the magnetic moment appears to increase with the doping concentration, at least at certain impurity separations, which is a positive indicator for practical applications.

  5. The mineralogy and mineral associations of platinum group elements and gold in the Platreef at Zwartfontein, Akanani Project, Northern Bushveld Complex, South Africa

    NASA Astrophysics Data System (ADS)

    van der Merwe, Frits; Viljoen, Fanus; Knoper, Mike

    2012-09-01

    The mineralogy of the platinum-group elements (PGE), and gold, in the Platreef of the Bushveld Complex, was investigated using an FEI Mineral Liberation Analyser. Polished sections were prepared from 171 samples collected from two boreholes, for the in-situ examination of platinum group minerals (PGM). PGM and gold minerals encountered include maslovite (PtBiTe, 32 area% of total PGM), kotulskite (Pd(BiTe), 17 %), isoferroplatinum (Pt3Fe, 15 %), sperrylite (PtAs2, 11 %), cooperite (PtS, 5 %), moncheite (PtTe2; 5 %), electrum (AuAg; 5 %), michenerite (PdBiTe; 3 %), Pd alloys (Pd, Sb, Sn; 3 %), hollingworthite ((Rh,Pt)AsS; 2 %), as well as minor (all <1 area% of total PGM) merenskyite (PdBiTe2), laurite (RuS2), rustenburgite (Pt0.4Pd0.4Sn0.2), froodite (PdBi2), atokite (Pd0.5Pt0.3Sn0.2), stumpflite (PtSb), plumbopalladinite (Pd3Pb2), and zvyagintsevite (Pd3Pb). An observed association of all PGM with base metal sulfides (BMS), and a pronounced association of PGE tellurides, arsenides and Pd&Pt alloys with secondary silicates, is consistent with the remobilisation and recrystallisation of some of the PGM's during hydrothermal alteration and serpentinisation subsequent to their initial (primary) crystallisation from BMS (e.g. Godel et al. J Petrol 48:1569-1604, 2007; Hutchinson and McDonald Appl Earth Sci (Trans Inst Min Metall B) 114:B208-224, 2008).

  6. Platinum-group element distribution in base-metal sulfides of the UG2 chromitite, Bushveld Complex, South Africa—a reconnaissance study

    NASA Astrophysics Data System (ADS)

    Osbahr, Inga; Oberthür, Thomas; Klemd, Reiner; Josties, Anja

    2014-08-01

    Two drill cores of the UG2 chromitite from the eastern and western Bushveld Complex were studied by whole-rock analysis, ore microscopy, SEM/Mineral Liberation Analysis (MLA), and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) analysis. The top and base of the UG2 main seam have the highest bulk-rock Pd and Pt concentrations. Sulfides mostly occur as aggregates of pentlandite, chalcopyrite, and rare pyrrhotite and pyrite or as individual grains associated mostly with chromite grains. In situ LA-ICP-MS analyses reveal that pentlandite carries distinctly elevated platinum-group element (PGE) contents. In contrast, pyrrhotite and chalcopyrite contain very low PGE concentrations. Pentlandite shows average maximum values of 350-1,000 ppm Pd, 200 ppm Rh, 130-175 ppm Ru, 20 ppm Os, and 150 ppm Ir, and is the principal host of Pd and Rh in the studied ores of the UG2. Mass balance calculations were conducted for samples representing the UG2 main seam of the drill core DT46, eastern Bushveld. Pentlandite consistently hosts elevated contents of the whole-rock Pd (up to 55 %) and Rh (up to 46 %), and erratic contents of Os (up to 50 %), Ir (2 to 17 %), and Ru (1-39 %). Platinum-group mineral (PGM) investigations support these mass balance results; most of the PGM are Pt-dominant such as braggite/cooperite and Pt-Fe alloys or laurite (carrying elevated concentrations of Os and Ir). Palladium and Rh-bearing PGM are rare. Both PGE concentrations and their distribution in base-metal sulfides (BMS) in the UG2 largely resemble that of the Merensky Reef, as most of the Pd and Rh are incorporated in pentlandite, whereas pyrrhotite, chalcopyrite, and pyrite are almost devoid of PGE.

  7. Determination of the platinum - Group elements (PGE) and gold (Au) in manganese nodule reference samples by nickel sulfide fire-assay and Te coprecipitation with ICP-MS

    USGS Publications Warehouse

    Balaram, V.; Mathur, R.; Banakar, V.K.; Hein, J.R.; Rao, C.R.M.; Gnaneswara, Rao T.; Dasaram, B.

    2006-01-01

    Platinum group elements (PGE) and Au data in polymetallic oceanic ferromanganese nodule reference samples and crust samples obtained by inductively coupled plasma mass spectrometry (ICP-MS), after separation and pre-concentration by nickel sulfide fire-assay and Te coprecipitation, are presented. By optimizing several critical parameters such as flux composition, matrix matching calibration, etc., best experimental conditions were established to develop a method suitable for routine analysis of manganese nodule samples for PGE and Au. Calibrations were performed using international PGE reference materials, WMG-1 and WMS-1. This improved procedure offers extremely low detection limits in the range of 0.004 to 0.016 ng/g. The results obtained in this study for the reference materials compare well with previously published data wherever available. New PGE data arc also provided on some international manganese nodule reference materials. The analytical methodology described here can be used for the routine analysis of manganese nodule and crust samples in marine geochemical studies.

  8. Systematically convergent basis sets with relativistic pseudopotentials. II. Small-core pseudopotentials and correlation consistent basis sets for the post-d group 16-18 elements

    SciTech Connect

    Peterson, Kirk A.; Figgen, Detlev; Goll, Erich; Stoll, Hermann; Dolg, Michael F.

    2003-12-01

    Series of correlation consistent basis sets have been developed for the post-d group 16-18 elements in conjunction with small-core relativistic pseudopotentials (PPs) of the energy-consistent variety. The latter were adjusted to multiconfiguration Dirac-Hartree-Fock data based on the Dirac-Coulomb-Breit Hamiltonian. The outer-core (n-1)spd shells are explicitly treated together with the nsp valence shell with these PPs. The accompanying cc-pVnZ-PP and aug-cc-pVnZ-PP basis sets range in size from DZ to 5Z quality and yield systematic convergence of both Hartree-Fock and correlated total energies. In addition to the calculation of atomic electron affinities and dipole polarizabilities of the rare gas atoms, numerous molecular benchmark calculations (HBr, HI, HAt, Br2, I2, At2, SiSe, SiTe, SiPo, KrH+, XeH+, and RnH+) are also reported at the coupled cluster level of theory. For the purposes of comparison, all-electron calculations using the Douglas-Kroll-Hess Hamiltonian have also been carried out for the halogen-containing molecules using basis sets of 5Z quality.

  9. The pH-dependent release of platinum group elements (PGEs) from gasoline and diesel fuel catalysts: Implication for weathering in soils.

    PubMed

    Suchá, Veronika; Mihaljevič, Martin; Ettler, Vojtěch; Strnad, Ladislav

    2016-04-15

    Powdered samples of new and old gasoline catalysts (Pt, Pd, Rh) and new and old diesel (Pt) catalysts were subjected to a pH-static leaching procedure (pH 2-9) coupled with thermodynamic modeling using PHREEQC-3 to verify the release and mobility of PGEs (platinum group elements). PGEs were released under acidic conditions, mostly exhibiting L-shaped leaching patterns: diesel old: 5.47, 0.005, 0.02; diesel new: 68.5, 0.23, 0.11; gasoline old: 0.1, 11.8, 4.79; gasoline new 2.6, 25.2, 35.9 in mg kg(-1) for Pt, Pd and Rh, respectively. Only the new diesel catalyst had a strikingly different leaching pattern with elevated concentrations at pH 4, probably influenced by the dissolution of the catalyst carrier and washcoat. The pH-static experiment coupled with thermodynamic modeling was found to be an effective instrument for understanding the leaching behavior of PGEs under various environmental conditions, and indicated that charged Pt and Rh species may be adsorbed on the negatively charged surface of kaolinite or Mn oxides in the soil system, whereas uncharged Pd and Rh species may remain mobile in soil solutions.

  10. Distribution and mineralogy of platinum-group elements in altered chromitites of the Campo Formoso layered intrusion (Bahia State, Brazil): control by magmatic and hydrothermal processes

    NASA Astrophysics Data System (ADS)

    Garuti, G.; Proenza, J. A.; Zaccarini, F.

    2007-03-01

    Polyphase, penetrative hydrothermal metasomatism in chromitites of the Campo Formoso layered intrusion produced spectacular chromite - ferrian chromite zoning and transformed the primary intercumulus silicates into a chlorite - serpentine - carbonate - talc assemblage. Alteration did not substantially modify the composition of chromite cores and the distribution of platinum-group elements (PGE) through the sequence of chromitite layers, which still are consistent with magmatic fractionation processes. Texture and composition of laurite and Os-Ir-Ru alloys included in chromite cores indicate that these PGM were not altered, and are probably magmaticin origin. In contrast, the PGM located in the intergranular chlorite matrix (laurite, Ir-Ru-Rh sulfarsenides and Pt-Pd compounds with Sb, Bi and Te) display evidence of hydrothermal reworking. These PGM are intimately intergrown with low-temperature Ni-sulfides. The paragenesis suggests that the Ni-sulfides-PGM assemblage formed at the expenses of unknown PGM precursors, which must have been originally present in the intercumulus silicate matrix. Mechanism of formation involves a sequence of dissolution-precipitation events controlled by variation of redox conditions during chromite alteration. The presence of a secondary ore mineral assemblage consisting of galena, bismuthinite, native antimony, and various Pb-Sb compounds suggests a possible contribution of fluids derived from the adjacent granite.

  11. Platinum-group elements in sewage sludge and incinerator ash in the United Kingdom: assessment of PGE sources and mobility in cities.

    PubMed

    Jackson, M T; Prichard, H M; Sampson, J

    2010-02-15

    Platinum-group element (PGE) concentrations in sewage sludge and incinerator ash compared with average PGE concentrations in road dust show a common pattern, characterized by a negative Rh anomaly. This similarity, found at 9 UK incinerators, suggests that there is a universal characteristic PGE pattern produced by common processes of dispersal of Pt, Pd and Rh derived from automobile catalytic converters. Ninety-one sewage sludge and incinerator ash samples from the sewage treatment facilities in Sheffield, Birmingham and 7 other UK cities were analyzed for PGE. The highest concentrations are 602ppb Pt and 710ppb Pd with lower maximum concentrations of 65ppb Rh, 100ppb Ru, 33ppb Ir and 12ppb Os. Ash from incinerated sewage was found to have higher PGE concentrations compared to the original sludge and the PGE ratios are preserved during incineration. Rh is more mobilized and dispersed than the other PGE as it is transported from roads into the drainage system and into sewage. Pt/Pd ratios of 1.0 in road dust and 0.9 in sewage and incinerator ash suggest that Pd is more mobile than Pt during dispersal. PGE abundances in stored incinerator ash of varying ages appear to have been affected by the variation in use of Pt, Pd and Rh in catalytic converters due to variation in their market prices. Concentrations of Os, Ir and Ru in ashes are greater in Sheffield and London than all the other city sites and may be derived from point industrial sources.

  12. Methods for forming group III-arsenide-nitride semiconductor materials

    NASA Technical Reports Server (NTRS)

    Major, Jo S. (Inventor); Welch, David F. (Inventor); Scifres, Donald R. (Inventor)

    2002-01-01

    Methods are disclosed for forming Group III-arsenide-nitride semiconductor materials. Group III elements are combined with group V elements, including at least nitrogen and arsenic, in concentrations chosen to lattice match commercially available crystalline substrates. Epitaxial growth of these III-V crystals results in direct bandgap materials, which can be used in applications such as light emitting diodes and lasers. Varying the concentrations of the elements in the III-V crystals varies the bandgaps, such that materials emitting light spanning the visible spectra, as well as mid-IR and near-UV emitters, can be created. Conversely, such material can be used to create devices that acquire light and convert the light to electricity, for applications such as full color photodetectors and solar energy collectors. The growth of the III-V crystals can be accomplished by growing thin layers of elements or compounds in sequences that result in the overall lattice match and bandgap desired.

  13. Orbital and physical parameters of eclipsing binaries from the ASAS catalogue - VII. V1200 Centauri: a bright triple in the Hyades moving group

    NASA Astrophysics Data System (ADS)

    Coronado, J.; Hełminiak, K. G.; Vanzi, L.; Espinoza, N.; Brahm, R.; Jordán, A.; Catelan, M.; Ratajczak, M.; Konacki, M.

    2015-04-01

    We present the orbital and physical parameters of the detached eclipsing binary V1200 Centauri (ASAS J135218-3837.3) from the analysis of spectroscopic observations and light curves from the All-Sky Automated Survey (ASAS) and SuperWASP (Wide Angle Search for Planets) data base. The radial velocities were computed from the high-resolution spectra obtained with the OUC (Observatorio Universidad Católica) 50-cm telescope and PUCHEROS (Pontificia Universidad Católica High Echelle Resolution Optical Spectrograph) spectrograph and with 1.2-m Euler telescope and CORALIE spectrograph using the cross-correlation technique TODCOR. We found that the absolute parameters of the system are M1 = 1.394 ± 0.030 M⊙, M2 = 0.866 ± 0.015 M⊙, R1 = 1.39 ± 0.15 R⊙, R2 = 1.10 ± 0.25 R⊙. We investigated the evolutionary status and kinematics of the binary and our results indicate that V1200 Centauri is likely a member of the Hyades moving group, but the largely inflated secondary's radius may suggest that the system may be even younger, around 30 Myr. We also found that the eclipsing pair is orbited by another, stellar-mass object on a 351-d orbit, which is unusually short for hierarchical triples. This makes V1200 Cen a potentially interesting target for testing the formation models of multiple stars.

  14. Evolution in an autopolyploid group displaying predominantly bivalent pairing at meiosis: genomic similarity of diploid Vaccinium darrowi and autotetraploid V. corymbosum (Ericaceae).

    PubMed

    Qu, L; Hancock, J; Whallon, J

    1998-05-01

    The genomic relationship between V. darrowi Camp (2n = 2x = 24) and V. corymbosum L. (2n = 4x = 48) was examined using an interspecific tetraploid hybrid, US 75, and representatives of the parental species. Two features in the background of US 75 led to the prediction that it was an allopolyploid: (1) the parental species are quite distinct morphologically and geographically, and (2) the diploid genome was incorporated into US 75 via an unreduced gamete. However, US 75 recently was shown to display tetrasomic inheritance using molecular markers. In the present cytological study, US 75 was found to have a lower than expected number of multivalents for an autopolyploid, although it had a significantly higher number of quadrivalents than its autotetraploid parent, V. corymbosum. Normal chromosome distributions were observed at anaphase I and II, and pollen viability was high. Our findings suggest that little genomic divergence has developed between the Vaccinium species and that the polyploids may freely exchange genes with sympatric diploid species via unreduced gametes. This pattern of hybridization could be an important component of evolution in all autopolyploid groups, making them much more dynamic than traditionally assumed.

  15. GENERAL REGULARITIES OF FORMATION OF CRYSTAL STRUCTURES OF ELEMENTS DEPENDING ON ELECTRON STRUCTURE OF ATOMS (OBSHCHILE ZAKONOMERNOSTI OBRAZOVANIYA KRISTALLICHESKIKH STRUKTUR ELEMENTOV V ZAVISIMOSTI OT ELEKTRONNOGO STROENIYA ATOMOV),

    DTIC Science & Technology

    A table is given showing the dependence of crystalline structures of elements on the number of electrons in the incompleted electronic subshells of...its atoms. The conclusion is drawn that the types of crystalline structures of the elements depend on the configuration of the outer electronic...subshells acquired by the atoms prior to crystallization. Crystalline structures of elements not governed by the 8 - N rule are determined by one or both

  16. A set of d-polarization functions for pseudo-potential basis sets of the main group elements AlBi and f-type polarization functions for Zn, Cd, Hg

    NASA Astrophysics Data System (ADS)

    Höllwarth, A.; Böhme, M.; Dapprich, S.; Ehlers, A. W.; Gobbi, A.; Jonas, V.; Köhler, K. F.; Stegmann, R.; Veldkamp, A.; Frenking, G.

    1993-06-01

    A set of five-component d-type polarization functions has been optimized for the main group elements AlBi at the energetically lowest lying s 2p n electronic states for use with the effective core potentials of Hay and Wadt at the CISD level of theory. Also a set of f-type polarization functions is suggested for the elements Zn, Cd and Hg.

  17. Platinum-group elements in the Merensky reef. I. PGE in solid solution in base metal sulfides and the down-temperature equilibration history of Merensky ores

    NASA Astrophysics Data System (ADS)

    Ballhaus, C.; Ryan, C. G.

    1995-12-01

    The platinum-group elements (PGE) in base metal sulfides (BMS) of the Merensky reef are mostly close to the detection limit of the proton microprobe. The only phase that accommodates appreciable PGE is pentlandite. Total average PGE plus Au grades of the sulfide fraction of the Merensky reef are about 500 ppm. We estimate the modal proportions of the major BMS to be around 53 percent pyrrhotite, 25 percent pentlandite, and 22 percent chalcopyrite (ignoring minor phases). Using this estimate, we calculate by how much the sulfides are oversaturated with respect to individual PGE. With respect to Pt, the sulfides are many times oversaturated, i.e., nearly all Pt occurs as discrete PGE phases. With regard to Pd the sulfides are oversaturated by about a factor of two. The Ru and Rh levels are at and below saturation levels. Available experiments suggest that the entire PGE content of the sulfide fraction can easily be accommodated in solid solution in BMS at temperatures as low as 500°C. The fact that the BMS are oversaturated with most PGE thus indicates that the sulfides have continued to exsolve PGE below that temperature. Calculated sulfur fugacities indicate that f S2 is controlled by silica activity, as expected in high-temperature ores, suggesting that metal/sulfur ratios of the ore may not have changed much since complete solidification of the intercumulus silicate melt of the Merensky reef. All sulfides investigated have cooled below the maximum temperature of pentlandite-pyrite coexistence, which experiments place at 250±30°C. Final closure temperatures of the sulfide-PGE mineral assemblages, approximated by extrapolating the pentlandite-pyrrhotite solvus beyond its experimentally determined range, are possibly as low as 80 to 90°C.

  18. How Accurate Are the Minnesota Density Functionals for Noncovalent Interactions, Isomerization Energies, Thermochemistry, and Barrier Heights Involving Molecules Composed of Main-Group Elements?

    PubMed

    Mardirossian, Narbe; Head-Gordon, Martin

    2016-09-13

    The 14 Minnesota density functionals published between the years 2005 and early 2016 are benchmarked on a comprehensive database of 4986 data points (84 data sets) involving molecules composed of main-group elements. The database includes noncovalent interactions, isomerization energies, thermochemistry, and barrier heights, as well as equilibrium bond lengths and equilibrium binding energies of noncovalent dimers. Additionally, the sensitivity of the Minnesota density functionals to the choice of basis set and integration grid is explored for both noncovalent interactions and thermochemistry. Overall, the main strength of the hybrid Minnesota density functionals is that the best ones provide very good performance for thermochemistry (e.g., M06-2X), barrier heights (e.g., M08-HX, M08-SO, MN15), and systems heavily characterized by self-interaction error (e.g., M06-2X, M08-HX, M08-SO, MN15), while the main weakness is that none of them are state-of-the-art for the full spectrum of noncovalent interactions and isomerization energies (although M06-2X is recommended from the 10 hybrid Minnesota functionals). Similarly, the main strength of the local Minnesota density functionals is that the best ones provide very good performance for thermochemistry (e.g., MN15-L), barrier heights (e.g., MN12-L), and systems heavily characterized by self-interaction error (e.g., MN12-L and MN15-L), while the main weakness is that none of them are state-of-the-art for the full spectrum of noncovalent interactions and isomerization energies (although M06-L is clearly the best from the four local Minnesota functionals). As an overall guide, M06-2X and MN15 are perhaps the most broadly useful hybrid Minnesota functionals, while M06-L and MN15-L are perhaps the most broadly useful local Minnesota functionals, although each has different strengths and weaknesses.

  19. Differences in the activities of eight enzymes from ten soil fungi and their possible influences on the surface structure, functional groups, and element composition of soil colloids.

    PubMed

    Wang, Wenjie; Li, Yanhong; Wang, Huimei; Zu, Yuangang

    2014-01-01

    How soil fungi function in soil carbon and nutrient cycling is not well understood by using fungal enzymatic differences and their interactions with soil colloids. Eight extracellular enzymes, EEAs (chitinase, carboxymethyl cellulase, β-glucosidase, protease, acid phosphatase, polyphenol oxidase, laccase, and guaiacol oxidase) secreted by ten fungi were compared, and then the fungi that showed low and high enzymatic activity were co-cultured with soil colloids for the purpose of finding fungi-soil interactions. Some fungi (Gomphidius rutilus, Russula integra, Pholiota adiposa, and Geastrum mammosum) secreted 3-4 enzymes with weak activities, while others (Cyathus striatus, Suillus granulate, Phallus impudicus, Collybia dryophila, Agaricus sylvicola, and Lactarius deliciosus) could secret over 5 enzymes with high activities. The differences in these fungi contributed to the alterations of functional groups (stretching bands of O-H, N-H, C-H, C = O, COO- decreased by 11-60%, while P = O, C-O stretching, O-H bending and Si-O-Si stretching increased 9-22%), surface appearance (disappearance of adhesive organic materials), and elemental compositions (11-49% decreases in C1s) in soil colloids. Moreover, more evident changes were generally in high enzymatic fungi (C. striatus) compared with low enzymatic fungi (G. rutilus). Our findings indicate that inter-fungi differences in EEA types and activities might be responsible for physical and chemical changes in soil colloids (the most active component of soil matrix), highlighting the important roles of soil fungi in soil nutrient cycling and functional maintenance.

  20. Differences in the Activities of Eight Enzymes from Ten Soil Fungi and Their Possible Influences on the Surface Structure, Functional Groups, and Element Composition of Soil Colloids

    PubMed Central

    Wang, Wenjie; Li, Yanhong; Wang, Huimei; Zu, Yuangang

    2014-01-01

    How soil fungi function in soil carbon and nutrient cycling is not well understood by using fungal enzymatic differences and their interactions with soil colloids. Eight extracellular enzymes, EEAs (chitinase, carboxymethyl cellulase, β-glucosidase, protease, acid phosphatase, polyphenol oxidase, laccase, and guaiacol oxidase) secreted by ten fungi were compared, and then the fungi that showed low and high enzymatic activity were co-cultured with soil colloids for the purpose of finding fungi-soil interactions. Some fungi (Gomphidius rutilus, Russula integra, Pholiota adiposa, and Geastrum mammosum) secreted 3–4 enzymes with weak activities, while others (Cyathus striatus, Suillus granulate, Phallus impudicus, Collybia dryophila, Agaricus sylvicola, and Lactarius deliciosus) could secret over 5 enzymes with high activities. The differences in these fungi contributed to the alterations of functional groups (stretching bands of O-H, N-H, C-H, C = O, COO- decreased by 11–60%, while P = O, C-O stretching, O-H bending and Si-O-Si stretching increased 9–22%), surface appearance (disappearance of adhesive organic materials), and elemental compositions (11–49% decreases in C1s) in soil colloids. Moreover, more evident changes were generally in high enzymatic fungi (C. striatus) compared with low enzymatic fungi (G. rutilus). Our findings indicate that inter-fungi differences in EEA types and activities might be responsible for physical and chemical changes in soil colloids (the most active component of soil matrix), highlighting the important roles of soil fungi in soil nutrient cycling and functional maintenance. PMID:25398013

  1. Experimental observations on noble metal nanonuggets and Fe-Ti oxides, and the transport of platinum group elements in silicate melts

    NASA Astrophysics Data System (ADS)

    Anenburg, Michael; Mavrogenes, John A.

    2016-11-01

    Platinum group element (PGE) nanonuggets are a nuisance in experimental studies designed to measure solubility or partitioning of noble metals in silicate melts. Instead of treating nanonuggets as experimental artifacts, we studied their behaviour motivated by recent discoveries of PGE nanonuggets in a variety of natural settings. We used an experimental setup consisting of AgPd, Pt or AuPd capsules and Fe(-Ti) oxide-saturated hydrous peralkaline silicate melts to maximise nanonugget production. TABS (Te, As, Bi, Sb, Sn) commonly occur in PGM (platinum group minerals), prompting addition of Bi to our experiments to investigate its properties as well. Three-dimensional optical examination by 100× objective and immersion oil reveals variable colour which correlates with nanonugget size and shape due to plasmon resonance effects. We observe two textural types: (1) intermediate-sized nanonuggets dispersed in the glass and adhering to oxides, and (2) abundant fine nanonuggets dispersed in the glass with coarse euhedral crystals in contact with oxides. Slow cooling removes dispersed nanonuggets and greatly coarsens existing oxide-associated metal crystals. Nanonugget-free halos are commonly observed around oxide grains. All metal phases are composed of major (Ag, Pd) and trace (Pt, Ir, Au) capsule material. Our results show reduction processes, imposed by growing oxides, causing local metal saturation in the oxide rich zones with preferential nucleation on smaller oxide grains. The redox gradient then blocks additional metals from diffusing into oxide rich zones, forming halos. As the entire experimental charge is reduced throughout the run, nanonuggets form in the distal glass. Bismuth contents of metal phases do not depend on Bi2O3 amounts dissolved in the melt. Further PGM crystallisation consumes nanonuggets as feedstock. We conclude that the appearance of metallic PGE phases happens in two stages: first as nanonuggets and then as larger PGM. Once formed

  2. Batisivite, V8Ti6[Ba(Si2O)]O28, a new mineral species from the derbylite group

    NASA Astrophysics Data System (ADS)

    Reznitsky, L. Z.; Sklyarov, E. V.; Armbruster, T.; Galuskin, E. V.; Ushchapovskaya, Z. F.; Polekhovsky, Yu. S.; Karmanov, N. S.; Kashaev, A. A.; Barash, I. G.

    2008-12-01

    Batisivite has been found as an accessory mineral in the Cr-V-bearing quartz-diopside metamorphic rocks of the Slyudyanka Complex in the southern Baikal region, Russia. A new mineral was named after the major cations in its ideal formula (Ba, Ti, Si, V). Associated minerals are quartz, Cr-V-bearing diopside and tremolite; calcite; schreyerite; berdesinskiite; ankangite; V-bearing titanite; minerals of the chromite-coulsonite, eskolaite-karelianite, dravite-vanadiumdravite, and chernykhite-roscoelite series; uraninite; Cr-bearing goldmanite; albite; barite; zircon; and unnamed U-Ti-V-Cr phases. Batisivite occurs as anhedral grains up to 0.15-0.20 mm in size, without visible cleavage and parting. The new mineral is brittle, with conchoidal fracture. Observed by the naked eye, the mineral is black and opaque, with a black streak and resinous luster. Batisivite is white in reflected light. The microhardness (VHN) is 1220-1470 kg/mm2 (load is 30 g), the mean value is 1330 kg/mm2. The Mohs hardness is near 7. The calculated density is 4.62 g/cm3. The new mineral is weakly anisotropic and bireflected. The measured values of reflectance are as follows (λ, nm— R {max/'}/ R {min/'}): 440—17.5/17.0; 460—17.3/16.7; 480—17.1/16.5; 500—17.2/16.6; 520—17.3/16.7; 540—17.4/16.8; 560—17.5/16.8; 580—17.6/16.9; 600—17.7/17.1; 620—17.7/17.1; 640—17.8/17.1; 660—17.9/17.2; 680—18.0/17.3; 700—18.1/17.4. Batisivite is triclinic, space group P overline 1 ; the unit-cell dimensions are: a = 7.521(1) Å, b = 7.643(1) Å, c = 9.572(1) Å, α = 110.20°(1), β = 103.34°(1), γ = 98.28°(1), V = 487.14(7) Å3, Z = 1. The strongest reflections in the X-ray powder diffraction pattern [ d, Å ( I, %)( hkl)] are: 3.09(8)(12 overline 2 ); 2.84, 2.85(10)(021, 120); 2.64(8)(21 overline 3 ); 2.12(8)(31 overline 3 ); 1.785(8)(32 overline 4 ), 1.581(10)(24 overline 2 ); 1.432, 1.433(10)(322, 124). The chemical composition (electron microprobe, average of 237 point analyses

  3. Assessment of Degree of Applicability of Benchmarks for Gadolinium Using KENO V.a and the 238-Group SCALE Cross-Section Library

    SciTech Connect

    Goluoglu, S.

    2003-12-01

    A review of the degree of applicability of benchmarks containing gadolinium using the computer code KENO V.a and the gadolinium cross sections from the 238-group SCALE cross-section library has been performed for a system that contains {sup 239}Pu, H{sub 2}O, and Gd{sub 2}O{sub 3}. The system (practical problem) is a water-reflected spherical mixture that represents a dry-out condition on the bottom of a sludge receipt and adjustment tank around steam coils. Due to variability of the mixture volume and the H/{sup 239}Pu ratio, approximations to the practical problem, referred to as applications, have been made to envelop possible ranges of mixture volumes and H/{sup 239}Pu ratios. A newly developed methodology has been applied to determine the degree of applicability of benchmarks as well as the penalty that should be added to the safety margin due to insufficient benchmarks.

  4. Catalytic one-electron reduction of uranyl(VI) to Group 1 uranyl(V) complexes via Al(III) coordination.

    PubMed

    Zegke, Markus; Nichol, Gary S; Arnold, Polly L; Love, Jason B

    2015-04-07

    Reactions between the uranyl(VI) Pacman complex [(UO2)(py)(H2L)] of the Schiff-base polypyrrolic macrocycle L and Tebbe's reagent or DIBAL result in the first selective reductive functionalisation of the uranyl oxo by Al to form [(py)(R2AlOUO)(py)(H2L)] (R = Me or (i)Bu). The clean displacement of the oxo-coordinated Al(III) by Group 1 cations has enabled the development of a one-pot, DIBAL-catalysed reduction of the U(VI) uranyl complexes to a series of new, mono-oxo alkali-metal-functionalised uranyl(V) complexes [(py)3(MOUO)(py)(H2L)] (M = Li, Na, K).

  5. Elemental abundance analyses with coadded DAO spectrograms. IV - Revision of previous analyses. V - The mercury-manganese stars Phi Herculis, 28 Herculis and HR 7664

    NASA Technical Reports Server (NTRS)

    Adelman, Saul J.

    1988-01-01

    Changes in chromium, manganese, and nickel abundances derived from singly ionized lines are incorporated into the elemental abundance of Adelman and Hill (1987) in order to provide more accurate gf values and damping constants for several atomic species. An improved agreement with the values from neutral lines of the same element is found. In the second part, the method is applied to an elemental abundance analysis of three mercury-manganese stars, and correlations are found between the derived abundances and the effective temperature.

  6. Platinum-group elements (PGE) and Rhenium in Marine Sediments across the Cretaceous-Tertiary Boundary: Constraints on Re-PGE Transport in the Marine Environment

    NASA Technical Reports Server (NTRS)

    Lee, Cin-Ty Aeolus; Wasserburg, Gerald J.; Kyte, Frank T.

    2003-01-01

    The nature of Re-platinum-group element (PGE; Pt, Pd, Ir, Os, Ru) transport in the marine environment was investigated by means of marine sediments at and across the Cretaceous-Tertiary boundary (KTB) at two hemipelagic sites in Europe and two pelagic sites in the North and South Pacific. A traverse across the KTB in the South Pacific pelagic clay core found elevated levels of Re, Pt, Ir, Os, and Ru, each of which is approximately symmetrically distributed over a distance of approx. 1.8 m across the KTB. The Re-PGE abundance patterns are fractionated from chondritic relative abundances: Ru, Pt, Pd, and Re contents are slightly subchondritic relative to Ir, and Os is depleted by approx. 95% relative to chondritic Ir proportions. A similar depletion in Os (approx. 90%) was found in a sample of the pelagic KTB in the North Pacific, but it is enriched in Ru, Pt, Pd, and Re relative to Ir. The two hemipelagic KTB clays have near-chondritic abundance patterns. The approx. 1.8-m-wide Re-PGE peak in the pelagic South Pacific section cannot be reconciled with the fallout of a single impactor, indicating that postdepositional redistribution has occurred. The elemental profiles appear to fit diffusion profiles, although bioturbation could have also played a role. If diffusion had occurred over approx. 65 Ma, the effective diffusivities are approx. 10(exp -13)sq cm/s, much smaller than that of soluble cations in pore waters (approx. 10(exp -5) sq cm/s). The coupling of Re and the PGEs during redistribution indicates that postdepositional processes did not significantly fractionate their relative abundances. If redistribution was caused by diffusion, then the effective diffusivities are the same. Fractionation of Os from Ir during the KTB interval must therefore have occurred during aqueous transport in the marine environment. Distinctly subchondritic Os/Ir ratios throughout the Cenozoic in the South Pacific core further suggest that fractionation of Os from Ir in the marine

  7. Abundances of platinum group elements in native sulfur condensates from the Niuatahi-Motutahi submarine volcano, Tonga rear arc: Implications for PGE mineralization in porphyry deposits

    NASA Astrophysics Data System (ADS)

    Park, Jung-Woo; Campbell, Ian H.; Kim, Jonguk

    2016-02-01

    Some porphyry Cu-Au deposits, which are enriched in Pd, are potentially an economic source of Pd. Magmatic volatile phases are thought to transport the platinum group elements (PGEs) from the porphyry source magma to the point of deposition. However, the compatibilities of the PGEs in magmatic volatile phases are poorly constrained. We report PGE and Re contents in native sulfur condensates and associated altered dacites from the Niuatahi-Motutahi submarine volcano, Tonga rear arc, in order to determine the compatibility of PGEs and Re in magmatic volatile phases, and their mobility during secondary hydrothermal alteration. The native sulfur we analyzed is the condensate of a magmatic volatile phase exsolved from the Niuatahi-Motutahi magma. The PGEs are moderately enriched in the sulfur condensates in comparison to the associated fresh dacite, with enrichment factors of 11-285, whereas Au, Cu and Re are strongly enriched with enrichment factors of ∼20,000, ∼5000 and ∼800 respectively. Although the PGEs are moderately compatible into magmatic volatile phases, their compatibility is significantly lower than that of Au, Cu and Re. Furthermore, the compatibility of PGEs decrease in the order: Ru > Pt > Ir > Pd. This trend is also observed in condensates and sublimates from other localities. PGE mineralization in porphyry Cu-Au deposits is characterized by substantially higher Pd/Pt (∼7-60) and Pd/Ir (∼100-10,500) than typical orthomagmatic sulfide deposits (e.g. Pd/Pt ∼0.6 and Pd/Ir ∼20 for the Bushveld). It has previously been suggested that the high mobility of Pd, relative to the other PGEs, may account for the preferential enrichment of Pd in porphyry Cu-Au deposits. However, the low compatibility of Pd in the volatile phase relative to the other PGEs, shown in this study, invalidates this explanation. We suggest that the PGE geochemistry of Pd-rich Cu-Au deposits is principally derived from the PGE characteristics of the magma from which the ore

  8. Platinum-group elements in alpine-type ultramafic rocks and related chromite ores of the main ophiolite belt of the Urals

    NASA Astrophysics Data System (ADS)

    Volchenko, Yu. A.; Koroteev, V. A.; Neustroeva, I. I.

    2009-04-01

    On the basis of a representative collection of ultramafic rocks and chromite ores and a series of technological samples from the largest (Central and Western) deposits in the Rai-Iz massif of the Polar Urals and the Almaz-Zhemchuzhina and Poiskovy deposits in the Kempirsai massif of the southern Urals, the distribution and speciation of platinum-group elements (PGE) in various type sections of mafic-ultramafic massifs of the Main ophiolite belt of the Urals have been studied. Spectral-chemical and spectrophotometric analyses were carried out to estimate PGE in 700 samples of ultramafic rocks and chromite ores; 400 analyses of minerals from rocks, ores, and concentrates and 100 analyses of PGE minerals (PGM) in chromite ores and concentrates were performed using an electron microprobe. Near-chondritic and nonchondritic PGE patterns in chromitebearing sections have been identified. PGE mineralization has been established to occur in chromite ore from all parts of the mafic-ultramafic massifs in the Main ophiolite belt of the Urals. The PGE deposits and occurrences discovered therein are attributed to four types (Kraka, Kempirsai, Nurali-Upper Neiva, and Shandasha), which are different in mode of geological occurrence, geochemical specialization, and placer-forming capability. Fluid-bearing minerals of the pargasite-edenite series have been identified for the first time in the matrix of chromite ore of the Kempirsai massif (the Almaz-Zhemchuzhina deposit) and Voikar-Syn’ya massif (the Kershor deposit). The PGE grade in various types of chromite ore ranges from 0.1-0.2 to 1-2 g/t or higher. According to technological sampling, the average PGE grade in the largest deposits of the southeastern ore field of the Kempirsai massif is 0.5-0.7 g/t. Due to the occurrence of most PGE as PGM 10-100 mm in size and the proved feasibility of their recovery into nickel alloys, chromites of the Kempirsai massif can be considered a complex ore with elevated and locally high Os, Ir

  9. Relatively Long-Lived Dubnium Isotopes and Chemical Identification of Superheavy Elements

    NASA Astrophysics Data System (ADS)

    Tereshatov, E. E.; Bruchertseifer, H.; Voronyuk, M. G.; Starodub, G. Ya.; Petrushkin, O. V.; Dmitriev, S. N.

    2010-04-01

    The present study has been performed within the framework of experiments aimed at the investigation of chemical properties of long-lived Db isotopes in aqueous solutions. The isocratic anion exchange separations of group V elements in the solutions containing HF have been considered. Parameters of separation of dubnium homologues (Pa, Nb and Ta) in HF/HNO3 mixed solutions have been optimized. The procedure of separation of group V elements from multicomponent system has been suggested.

  10. Relatively Long-Lived Dubnium Isotopes and Chemical Identification of Superheavy Elements

    SciTech Connect

    Tereshatov, E. E.; Voronyuk, M. G.; Starodub, G. Ya.; Petrushkin, O. V.; Dmitriev, S. N.; Bruchertseifer, H.

    2010-04-30

    The present study has been performed within the framework of experiments aimed at the investigation of chemical properties of long-lived Db isotopes in aqueous solutions. The isocratic anion exchange separations of group V elements in the solutions containing HF have been considered. Parameters of separation of dubnium homologues (Pa, Nb and Ta) in HF/HNO{sub 3} mixed solutions have been optimized. The procedure of separation of group V elements from multicomponent system has been suggested.

  11. Platinum Group Elements, 187OS/188OS and 87SR/86SR Isotope Systematics in Depleted Fluid-Modified Mariana Fore-Arc Peridotites

    NASA Astrophysics Data System (ADS)

    Harvey, J.; Savov, I. P.; Shirey, S. B.; Horan, M. F.; Mock, T. D.

    2012-12-01

    The serpentine mud volcanoes of the Izu-Bonin-Mariana (IBM) fore-arc, collected during Ocean Drilling Program Leg 195 [1], contain hard-rock clasts of serpentine sampled from close to the décollement, which separates the down-going Pacific slab from the overlying mantle wedge. These clasts preserve evidence for melt depletion (>25 % melt extraction in many instances) in a sub-arc environment, and extensive (40 - 100%) serpentinization due to subsequent fluid / peridotite interaction, e.g. [2]. Platinum-group element (PGE) abundances are not consistent with melt-depletion alone [3]. Fractionation between I-PGE (Os, Ir, Ru) has resulted in groups of IBM serpentinites with either a high chondrite-normalized Os/Ir ratio (OsN/IrN) or a low OsN/IrN ratio. Similarly, fractionation of P-PGE (Pt, Pd) is marked, and distinguishes the IBM serpentinites from worldwide abyssal peridotites. Interaction with high-pH fluids [4] may have partially oxidized mantle sulphide, the major primary host for PGE in these rocks, leading to partial breakdown to sulphate and the selective redistribution of certain PGE (Os, Ru, Pt), a feature normally associated with sub-aerial weathering [5], but which likely prevails in other oxidizing environments. In particular, the Re-Os systematics of the high (OsN/IrN) IBM serpentinites have been disturbed by the addition of Os. Unlike peridotite xenoliths associated with magmatic regions of subduction zones where subduction-related Os-addition is unequivocally radiogenic and derived from crustal material [6][7], where Os has been added to the IBM serpentinites it is unradiogenic and was most likely derived from within the oceanic mantle. IBM serpentinites therefore preserve osmium isotope ratios that are exclusively sub-chondritic (187Os/188Os ≤ 0.127), as previously reported [8]. These serpentinized peridotites were produced by at least a three-step process: melt depletion, serpentinization, and the mobilization of Os, Ru and Pt to produce low Os

  12. The use of artificial neural network for modelling of phycoremediation of toxic elements As(III) and As(V) from wastewater using Botryococcus braunii

    NASA Astrophysics Data System (ADS)

    Podder, M. S.; Majumder, C. B.

    2016-02-01

    In the present study, a thorough investigation has been done on the removal efficiency of both As(III) and As (V) from synthetic wastewater by phycoremediation of Botryococcus braunii algal biomass. Artificial neural networks (ANNs) are practised for predicting % phycoremediation efficiency of both As(III) and As(V) ions. The influence of several parameters for example initial pH, inoculum size, contact time and initial arsenic concentration (either As(III) or As(V)) was examined systematically. The maximum phycoremediation of As(III) and As(V) was found to be 85.22% and 88.15% at pH 9.0, equilibrium time of 144 h by using algal inoculum size of 10% (v/v) and initial arsenic concentration of 50 mg/L. The data acquired from laboratory scale experimental set up was utilized for training a three-layer feed-forward back propagation (BP) with Levenberg-Marquardt (LM) training algorithm having 4:5:1 architecture. A comparison between the experimental data and model outputs provided a high correlation coefficient (R2all_ANN equal to 0.9998) and exhibited that the model was capable for predicting the phycoremediation of both As(III) and As(V) from wastewater. The network topology was optimized by changing number of neurons in hidden layers. ANNs are efficient to model and simulate highly non-liner multivariable relationships. Absolute error and Standard deviation (SD) with respect to experimental output were calculated for ANN model outputs. The comparison of phycoremediation efficiencies of both As(III) and As(V) between experimental results and ANN model outputs exhibited that ANN model can determine the behaviour of As(III) and As(V) elimination process under various circumstances.

  13. The use of artificial neural network for modelling of phycoremediation of toxic elements As(III) and As(V) from wastewater using Botryococcus braunii.

    PubMed

    Podder, M S; Majumder, C B

    2016-02-15

    In the present study, a thorough investigation has been done on the removal efficiency of both As(III) and As (V) from synthetic wastewater by phycoremediation of Botryococcus braunii algal biomass. Artificial neural networks (ANNs) are practised for predicting % phycoremediation efficiency of both As(III) and As(V) ions. The influence of several parameters for example initial pH, inoculum size, contact time and initial arsenic concentration (either As(III) or As(V)) was examined systematically. The maximum phycoremediation of As(III) and As(V) was found to be 85.22% and 88.15% at pH9.0, equilibrium time of 144h by using algal inoculum size of 10% (v/v) and initial arsenic concentration of 50mg/L. The data acquired from laboratory scale experimental set up was utilized for training a three-layer feed-forward back propagation (BP) with Levenberg-Marquardt (LM) training algorithm having 4:5:1 architecture. A comparison between the experimental data and model outputs provided a high correlation coefficient (R(2)all_ANN equal to 0.9998) and exhibited that the model was capable for predicting the phycoremediation of both As(III) and As(V) from wastewater. The network topology was optimized by changing number of neurons in hidden layers. ANNs are efficient to model and simulate highly non-liner multivariable relationships. Absolute error and Standard deviation (SD) with respect to experimental output were calculated for ANN model outputs. The comparison of phycoremediation efficiencies of both As(III) and As(V) between experimental results and ANN model outputs exhibited that ANN model can determine the behaviour of As(III) and As(V) elimination process under various circumstances.

  14. Albedo factors of some elements in the atomic number range 26≤Z≤79 for 59.54keV.

    PubMed

    Yılmaz, Demet; Uzunoğlu, Zeynep; Demir, Celalettin

    2017-04-01

    In this study, we aimed to determine the albedo factors for Fe, Co, Ni, Cu, Zr, Mo, Ag, Dy, Yb, and Au. Albedo factors were investigated experimentally for 59.54keV photon energy by using an HPGe detector with a resolution of 182eV at 5.9keV. Albedo number (AN), albedo energy (AE), and albedo dose (AD) were plotted as a function of atomic number of the target. It was observed that albedo factors decreased with increasing atomic number. In addition, there was a good third-order polynomial relationship between the albedo factors and atomic number.

  15. Determination of natural line widths of Kα X-ray lines for some elements in the atomic range 50≤Z≤65 at 59.5 keV

    NASA Astrophysics Data System (ADS)

    Kündeyi, Kadriye; Aylıkcı, Nuray Küp; Tıraşoǧlu, Engin; Kahoul, Abdelhalim; Aylıkcı, Volkan

    2017-02-01

    The semi-empirical determination of natural widths of Kα X-ray lines (Kα1 and Kα2) were performed for Sn, Sb, Te, I, Ba, La, Ce, Pr, Nd, Sm, Eu, Gd and Tb. For the semi-empirical determination of the line widths, K shell fluorescence yields of elements were measured. The samples were excited by 59.5 keV γ rays from a 241Am annular radioactive source in order to measure the K shell fluorescence yields. The emitted K X-rays from the samples were counted by an Ultra-LEGe detector with a resolution of 150 eV at 5.9 keV. The measured K shell fluorescence yields were used for the calculation of K shell level widths. Finally, the natural widths of K X-ray lines were determined as the sums of levels which involved in the transition. The obtained values were compared with earlier studies.

  16. Accelerator measurement of the energy spectra of neutrons emitted in the interaction of 3-GeV protons with several elements

    NASA Technical Reports Server (NTRS)

    Nalesnik, W. J.; Devlin, T. J.; Merker, M.; Shen, B. S. P.

    1972-01-01

    The application of time of flight techniques for determining the shapes of the energy spectra of neutrons between 20 and 400 MeV is discussed. The neutrons are emitted at 20, 34, and 90 degrees in the bombardment of targets by 3 GeV protons. The targets used are carbon, aluminum, cobalt, and platinum with cylindrical cross section. Targets being bombarded are located in the internal circulating beam of a particle accelerator.

  17. Multi-elemental characterization of tunnel and road dusts in Houston, Texas using dynamic reaction cell-quadrupole-inductively coupled plasma-mass spectrometry: evidence for the release of platinum group and anthropogenic metals from motor vehicles.

    PubMed

    Spada, Nicholas; Bozlaker, Ayse; Chellam, Shankararaman

    2012-07-20

    Platinum group elements (PGEs) including Rh, Pd, and Pt are important tracers for vehicular emissions, though their measurement is often challenging and difficult to replicate in environmental campaigns. These challenges arise from sample preparation steps required for PGE quantitation, which often cause severe isobaric interferences and spectral overlaps from polyatomic species of other anthropogenically emitted metals. Consequently, most previous road dust studies have either only quantified PGEs or included a small number of anthropogenic elements. Therefore a novel analytical method was developed to simultaneously measure PGEs, lanthanoids, transition and main group elements to comprehensively characterize the elemental composition of urban road and tunnel dusts. Dust samples collected from the vicinity of high-traffic roadways and a busy underwater tunnel restricted to single-axle (predominantly gasoline-driven) vehicles in Houston, TX were analyzed for 45 metals with the newly developed method using dynamic reaction cell-quadrupole-inductively coupled plasma-mass spectrometry (DRC-q-ICP-MS). Average Rh, Pd and Pt concentrations were 152±52, 770±208 and 529±130 ng g(-1) respectively in tunnel dusts while they varied between 6 and 8 ng g(-1), 10 and 88 ng g(-1) and 35 and 131 ng g(-1) in surface road dusts. Elemental ratios and enrichment factors demonstrated that PGEs in dusts originated from autocatalyst attrition/abrasion. Strong evidence is also presented for mobile source emissions of Cu, Zn, Ga, As, Mo, Cd, Sn, Sb, Ba, W and Pb. However, all other elements including rare earths most likely arose from weathering, erosion and resuspension of crustal material. These are the first such detailed measurements in Houston, the largest city in TX and fourth largest in the United States. We posit that such investigations will assist in better understanding PGE concentrations in urban environments while providing elemental data necessary to better understand

  18. Large-signal characterizations of DDR IMPATT devices based on group III-V semiconductors at millimeter-wave and terahertz frequencies

    NASA Astrophysics Data System (ADS)

    Acharyya, Aritra; Mallik, Aliva; Banerjee, Debopriya; Ganguli, Suman; Das, Arindam; Dasgupta, Sudeepto; Banerjee, J. P.

    2014-08-01

    Large-signal (L-S) characterizations of double-drift region (DDR) impact avalanche transit time (IMPATT) devices based on group III-V semiconductors such as wurtzite (Wz) GaN, GaAs and InP have been carried out at both millimeter-wave (mm-wave) and terahertz (THz) frequency bands. A L-S simulation technique based on a non-sinusoidal voltage excitation (NSVE) model developed by the authors has been used to obtain the high frequency properties of the above mentioned devices. The effect of band-to-band tunneling on the L-S properties of the device at different mm-wave and THz frequencies are also investigated. Similar studies are also carried out for DDR IMPATTs based on the most popular semiconductor material, i.e. Si, for the sake of comparison. A comparative study of the devices based on conventional semiconductor materials (i.e. GaAs, InP and Si) with those based on Wz-GaN shows significantly better performance capabilities of the latter at both mm-wave and THz frequencies.

  19. Critical role of phospholipase A2 group IID in age-related susceptibility to severe acute respiratory syndrome-CoV infection.

    PubMed

    Vijay, Rahul; Hua, Xiaoyang; Meyerholz, David K; Miki, Yoshimi; Yamamoto, Kei; Gelb, Michael; Murakami, Makoto; Perlman, Stanley

    2015-10-19

    Oxidative stress and chronic low-grade inflammation in the lungs are associated with aging and may contribute to age-related immune dysfunction. To maintain lung homeostasis, chronic inflammation is countered by enhanced expression of proresolving/antiinflammatory factors. Here, we show that age-dependent increases of one such factor in the lungs, a phospholipase A2 (PLA2) group IID (PLA2G2D) with antiinflammatory properties, contributed to worse outcomes in mice infected with severe acute respiratory syndrome-coronavirus (SARS-CoV). Strikingly, infection of mice lacking PLA2G2D expression (Pla2g2d(-/-) mice) converted a uniformly lethal infection to a nonlethal one (>80% survival), subsequent to development of enhanced respiratory DC migration to the draining lymph nodes, augmented antivirus T cell responses, and diminished lung damage. We also observed similar effects in influenza A virus-infected middle-aged Pla2g2d(-/-) mice. Furthermore, oxidative stress, probably via lipid peroxidation, was found to induce PLA2G2D expression in mice and in human monocyte-derived macrophages. Thus, our results suggest that directed inhibition of a single inducible phospholipase, PLA2G2D, in the lungs of older patients with severe respiratory infections is potentially an attractive therapeutic intervention to restore immune function.

  20. Critical role of phospholipase A2 group IID in age-related susceptibility to severe acute respiratory syndrome–CoV infection

    PubMed Central

    Vijay, Rahul; Hua, Xiaoyang; Meyerholz, David K.; Miki, Yoshimi; Yamamoto, Kei; Gelb, Michael; Murakami, Makoto

    2015-01-01

    Oxidative stress and chronic low-grade inflammation in the lungs are associated with aging and may contribute to age-related immune dysfunction. To maintain lung homeostasis, chronic inflammation is countered by enhanced expression of proresolving/antiinflammatory factors. Here, we show that age-dependent increases of one such factor in the lungs, a phospholipase A2 (PLA2) group IID (PLA2G2D) with antiinflammatory properties, contributed to worse outcomes in mice infected with severe acute respiratory syndrome-coronavirus (SARS-CoV). Strikingly, infection of mice lacking PLA2G2D expression (Pla2g2d−/− mice) converted a uniformly lethal infection to a nonlethal one (>80% survival), subsequent to development of enhanced respiratory DC migration to the draining lymph nodes, augmented antivirus T cell responses, and diminished lung damage. We also observed similar effects in influenza A virus–infected middle-aged Pla2g2d−/− mice. Furthermore, oxidative stress, probably via lipid peroxidation, was found to induce PLA2G2D expression in mice and in human monocyte–derived macrophages. Thus, our results suggest that directed inhibition of a single inducible phospholipase, PLA2G2D, in the lungs of older patients with severe respiratory infections is potentially an attractive therapeutic intervention to restore immune function. PMID:26392224

  1. Fabrication of a Core-Shell-Type Photocatalyst via Photodeposition of Group IV and V Transition Metal Oxyhydroxides: An Effective Surface Modification Method for Overall Water Splitting.

    PubMed

    Takata, Tsuyoshi; Pan, Chengsi; Nakabayashi, Mamiko; Shibata, Naoya; Domen, Kazunari

    2015-08-05

    The design of optimal surface structures for photocatalysts is a key to efficient overall water splitting into H2 and O2. A unique surface modification method was devised for a photocatalyst to effectively promote overall water splitting. Photodeposition of amorphous oxyhydroxides of group IV and V transition metals (Ti, Nb, Ta) over a semiconductor photocatalyst from corresponding water-soluble metal peroxide complexes was examined. In this method, amorphous oxyhydroxide covered the whole surface of the photocatalyst particles, creating a core-shell structure. The water splitting behavior of the novel core-shell-type photocatalyst in relation to the permeation behavior of the coating layer was investigated in detail. Overall water splitting proceeded successfully after the photodeposition, owing to the prevention of the reverse reaction. The photodeposited oxyhydroxide layers were found to function as molecular sieves, selectively filtering reactant and product molecules. By exploiting the selective permeability of the coating layer, redox reactions on the photocatalyst surface could be suitably controlled, which resulted in successful overall water splitting.

  2. Elemental abundance analyses with DAO spectrograms. XXVII. The superficially normal stars theta And (A2 IV), epsilon Del (B6 III), epsilon Aqr (A1.5 V), and iota And (B9 V)

    NASA Astrophysics Data System (ADS)

    Kocer, D.; Adelman, S. J.; Caliskan, H.; Gulliver, A. F.; Gokmen Tektunali, H.

    2003-08-01

    The superficially normal stars theta And (A2 V), epsilon Del (B6 III), epsilon Aqr (A1.5 V), and iota And (B9 V), which have rotationally broadened line profiles, are analyzed in a manner consistent with previous studies of this series using 2.4 Åmm-1 spectrograms obtained with CCD detectors and S/N >=200. Their variable radial velocities strongly suggest they are spectroscopic binaries. As no evidence is seen for lines of their companions they are analyzed as single stars. Their derived abundances are generally near solar. But those for theta And suggest that it is possibly a fast rotating Am star. Table 5 is only available in electronic form at the CDS via anonymous ftp to cdsarc.u-strasbg.fr (130.79.128.5) or via http://cdsweb.u-strasbg.fr/cgi-bin/qcat?J/A+A/406/975

  3. The Influence of Ni and V Trace Elements on High-Temperature Tensile Properties and Aging of A356 Aluminum Foundry Alloy

    NASA Astrophysics Data System (ADS)

    di Giovanni, Maria Teresa; Cerri, Emanuela; Casari, Daniele; Merlin, Mattia; Arnberg, Lars; Garagnani, Gian Luca

    2016-05-01

    High-temperature tensile properties of unmodified A356 alloy with and without the addition of Ni or V in traces (600 and 1000 ppm of Ni and V, respectively) were investigated by analyzing samples obtained from sand and permanent mold castings in the as-cast and T6 heat-treated conditions. Tensile tests were performed at 508 K (235 °C) at a crosshead speed of 1 mm/min. In addition, samples were subjected to artificial aging at 508 K (235 °C) for different times, and corresponding hardness curves were plotted. Microstructures and fracture surfaces, analyzed by FEG-SEM equipped with energy dispersive X-ray spectroscopy, showed that neither Ni nor V addition had a detrimental effect on high-temperature tensile properties. Aging curves showed a strong loss of hardness affecting the T6 class between 30-min and 1-h exposure time. After 6-h aging, no evidence of aging treatment persisted on hardness of the tested material. Hardness values did not reveal any significant difference between the reference alloy and the Ni- and V-containing alloys in both casting conditions, in complete analogy with the tensile properties. Unmodified eutectic silicon particles provided inhomogeneity in the α-Al matrix and acted as the principal source of stress concentration leading to fracture.

  4. TE-Locate: A Tool to Locate and Group Transposable Element Occurrences Using Paired-End Next-Generation Sequencing Data.

    PubMed

    Platzer, Alexander; Nizhynska, Viktoria; Long, Quan

    2012-09-12

    Transposable elements (TEs) are common mobile DNA elements present in nearly all genomes. Since the movement of TEs within a genome can sometimes have phenotypic consequences, an accurate report of TE actions is desirable. To this end, we developed TE-Locate, a computational tool that uses paired-end reads to identify the novel locations of known TEs. TE-Locate can utilize either a database of TE sequences, or annotated TEs within the reference sequence of interest. This makes TE-Locate useful in the search for any mobile sequence, including retrotransposed gene copies. One major concern is to act on the correct hierarchy level, thereby avoiding an incorrect calling of a single insertion as multiple events of TEs with high sequence similarity. We used the (super)family level, but TE-Locate can also use any other level, right down to the individual transposable element. As an example of analysis with TE-Locate, we used the Swedish population in the 1,001 Arabidopsis genomes project, and presented the biological insights gained from the novel TEs, inducing the association between different TE superfamilies. The program is freely available, and the URL is provided in the end of the paper.

  5. A Measurement of the Top Quark Mass with the D0 Detector at s**(1/2) = 1.96-TeV using the Matrix Element Method

    SciTech Connect

    Kroeninger, Kevin Alexander; /Bonn U.

    2004-04-01

    Using a data set of 158 and 169 pb{sup -1} of D0 Run-II data in the electron and muon plus jets channel, respectively, the top quark mass has been measured using the Matrix Element Method. The method and its implementation are described. Its performance is studied in Monte Carlo using ensemble tests and the method is applied to the Moriond 2004 data set.

  6. How Deep and Hot was Earth's Magma Ocean? Combined Experimental Datasets for the Metal-silicate Partitioning of 11 Siderophile Elements - Ni, Co, Mo, W, P, Mn, V, Cr, Ga, Cu and Pd

    NASA Technical Reports Server (NTRS)

    Righter, Kevin

    2008-01-01

    variable oxygen fugacity. Preliminary results confirm that D(Ni) and D(Co) converge at pressures near 25-30 GPa and approximately 2200 K, and show that D(Pd) and D(Cu) become too low at the PT conditions of the deepest models. Furthermore, models which force fit V and Cr mantle concentrations by metal-silicate equilibrium overlook the fact that at early Earth mantle fO2, these elements will be more compatible in Mg-perovskite and (Fe,Mg)O than in metal. Thus an intermediate depth magma ocean, at 25-30 GPa, 2200 K, and at IW-2, can explain more mantle siderophile element concentrations than other models.

  7. On Some Algebraic and Combinatorial Properties of Dunkl Elements

    NASA Astrophysics Data System (ADS)

    Kirillov, Anatol N.

    2013-06-01

    We introduce and study a certain class of nonhomogeneous quadratic algebras together with the special set of mutually commuting elements inside of each, the so-called Dunkl elements. We describe relations among the Dunkl elements. This result is a further generalization of similar results obtained in [S. Fomin and A. N. Kirillov, Quadratic algebras, Dunkl elements and Schubert calculus, in Advances in Geometry (eds. J.-S. Brylinski, V. Nistor, B. Tsygan and P. Xu), Progress in Math. Vol. 172 (Birkhäuser Boston, Boston, 1995), pp. 147-182, A. Postnikov, On a quantum version of Pieri's formula, in Advances in Geometry (eds. J.-S. Brylinski, R. Brylinski, V. Nistor, B. Tsygan and P. Xu), Progress in Math. Vol. 172 (Birkhäuser Boston, 1995), pp. 371-383 and A. N. Kirillov and T. Maenor, A Note on Quantum K-Theory of Flag Varieties, preprint]. As an application we describe explicitly the set of relations among the Gaudin elements in the group ring of the symmetric group, cf. [E. Mukhin, V. Tarasov and A. Varchenko, Bethe Subalgebras of the Group Algebra of the Symmetric Group, preprint arXiv:1004.4248]. Also we describe a few combinatorial properties of some special elements in the associative quasi-classical Yang-Baxter algebra in a connection with the values of the β-Grothendieck polynomials for some special permutations, and on the other hand, with the Ehrhart polynomial of the Chan-Robbins polytope.

  8. On Some Algebraic and Combinatorial Properties of Dunkl Elements

    NASA Astrophysics Data System (ADS)

    Kirillov, Anatol N.

    2012-11-01

    We introduce and study a certain class of nonhomogeneous quadratic algebras together with the special set of mutually commuting elements inside of each, the so-called Dunkl elements. We describe relations among the Dunkl elements. This result is a further generalization of similar results obtained in [S. Fomin and A. N. Kirillov, Quadratic algebras, Dunkl elements and Schubert calculus, in Advances in Geometry (eds. J.-S. Brylinski, V. Nistor, B. Tsygan and P. Xu), Progress in Math. Vol. 172 (Birkhäuser Boston, Boston, 1995), pp. 147-182, A. Postnikov, On a quantum version of Pieri's formula, in Advances in Geometry (eds. J.-S. Brylinski, R. Brylinski, V. Nistor, B. Tsygan and P. Xu), Progress in Math. Vol. 172 (Birkhäuser Boston, 1995), pp. 371-383 and A. N. Kirillov and T. Maenor, A Note on Quantum K-Theory of Flag Varieties, preprint]. As an application we describe explicitly the set of relations among the Gaudin elements in the group ring of the symmetric group, cf. [E. Mukhin, V. Tarasov and A. Varchenko, Bethe Subalgebras of the Group Algebra of the Symmetric Group, preprint arXiv:1004.4248]. Also we describe a few combinatorial properties of some special elements in the associative quasi-classical Yang-Baxter algebra in a connection with the values of the β-Grothendieck polynomials for some special permutations, and on the other hand, with the Ehrhart polynomial of the Chan-Robbins polytope.

  9. Spin-density matrix elements for γp→K*0Σ+ at Eγ=1.85-3.0 GeV with evidence for the κ(800) meson exchange.

    PubMed

    Hwang, S H; Hicks, K; Ahn, J K; Nakano, T; Ahn, D S; Chang, W C; Chen, J Y; Daté, S; Ejiri, H; Fujimura, H; Fujiwara, M; Fukui, S; Gohn, W; Hotta, T; Imai, K; Ishikawa, T; Joo, K; Kato, Y; Kohri, H; Kon, Y; Lee, H S; Maeda, Y; Miyabe, M; Mibe, T; Morino, Y; Muramatsu, N; Nakatsugawa, Y; Niiyama, M; Noumi, H; Oh, Y; Ohashi, Y; Ohta, T; Oka, M; Parker, J; Rangacharyulu, C; Ryu, S Y; Sawada, T; Sugaya, Y; Sumihama, M; Tsunemi, T; Uchida, M; Ungaro, M; Yosoi, M

    2012-03-02

    The exclusive reaction γp→K(+)π(-)Σ(+) was measured for the first time using linearly polarized photons at beam energies from 1.85 to 2.96 GeV. Angular distributions in the rest frame of the K(+)π(-) system were fitted to extract spin-density matrix elements of the K(*0) decay. The measured parity spin asymmetry shows that natural-parity exchange is dominant in this reaction. This result clearly indicates the need for t-channel exchange of the κ(800) scalar meson.

  10. Tevatron Combination of Single-Top-Quark Cross Sections and Determination of the Magnitude of the Cabibbo-Kobayashi-Maskawa Matrix Element V_{tb}.

    PubMed

    Aaltonen, T; Abazov, V M; Abbott, B; Acharya, B S; Adams, M; Adams, T; Agnew, J P; Alexeev, G D; Alkhazov, G; Alton, A; Amerio, S; Amidei, D; Anastassov, A; Annovi, A; Antos, J; Apollinari, G; Appel, J A; Arisawa, T; Artikov, A; Asaadi, J; Ashmanskas, W; Askew, A; Atkins, S; Auerbach, B; Augsten, K; Aurisano, A; Avila, C; Azfar, F; Badaud, F; Badgett, W; Bae, T; Bagby, L; Baldin, B; Bandurin, D V; Banerjee, S; Barbaro-Galtieri, A; Barberis, E; Baringer, P; Barnes, V E; Barnett, B A; Barria, P; Bartlett, J F; Bartos, P; Bassler, U; Bauce, M; Bazterra, V; Bean, A; Bedeschi, F; Begalli, M; Behari, S; Bellantoni, L; Bellettini, G; Bellinger, J; Benjamin, D; Beretvas, A; Beri, S B; Bernardi, G; Bernhard, R; Bertram, I; Besançon, M; Beuselinck, R; Bhat, P C; Bhatia, S; Bhatnagar, V; Bhatti, A; Bland, K R; Blazey, G; Blessing, S; Bloom, K; Blumenfeld, B; Bocci, A; Bodek, A; Boehnlein, A; Boline, D; Boos, E E; Borissov, G; Bortoletto, D; Borysova, M; Boudreau, J; Boveia, A; Brandt, A; Brandt, O; Brigliadori, L; Brock, R; Bromberg, C; Bross, A; Brown, D; Brucken, E; Bu, X B; Budagov, J; Budd, H S; Buehler, M; Buescher, V; Bunichev, V; Burdin, S; Burkett, K; Busetto, G; Bussey, P; Buszello, C P; Butti, P; Buzatu, A; Calamba, A; Camacho-Pérez, E; Camarda, S; Campanelli, M; Canelli, F; Carls, B; Carlsmith, D; Carosi, R; Carrillo, S; Casal, B; Casarsa, M; Casey, B C K; Castilla-Valdez, H; Castro, A; Catastini, P; Caughron, S; Cauz, D; Cavaliere, V; Cerri, A; Cerrito, L; Chakrabarti, S; Chan, K M; Chandra, A; Chapon, E; Chen, G; Chen, Y C; Chertok, M; Chiarelli, G; Chlachidze, G; Cho, K; Cho, S W; Choi, S; Chokheli, D; Choudhary, B; Cihangir, S; Claes, D; Clark, A; Clarke, C; Clutter, J; Convery, M E; Conway, J; Cooke, M; Cooper, W E; Corbo, M; Corcoran, M; Cordelli, M; Couderc, F; Cousinou, M-C; Cox, C A; Cox, D J; Cremonesi, M; Cruz, D; Cuevas, J; Culbertson, R; Cutts, D; Das, A; d'Ascenzo, N; Datta, M; Davies, G; de Barbaro, P; de Jong, S J; De La Cruz-Burelo, E; Déliot, F; Demina, R; Demortier, L; Deninno, M; Denisov, D; Denisov, S P; D'Errico, M; Desai, S; Deterre, C; DeVaughan, K; Devoto, F; Di Canto, A; Di Ruzza, B; Diehl, H T; Diesburg, M; Ding, P F; Dittmann, J R; Dominguez, A; Donati, S; D'Onofrio, M; Dorigo, M; Driutti, A; Dubey, A; Dudko, L V; Duperrin, A; Dutt, S; Eads, M; Ebina, K; Edgar, R; Edmunds, D; Elagin, A; Ellison, J; Elvira, V D; Enari, Y; Erbacher, R; Errede, S; Esham, B; Evans, H; Evdokimov, A; Evdokimov, V N; Farrington, S; Fauré, A; Feng, L; Ferbel, T; Fernández Ramos, J P; Fiedler, F; Field, R; Filthaut, F; Fisher, W; Fisk, H E; Flanagan, G; Forrest, R; Fortner, M; Fox, H; Franklin, M; Freeman, J C; Frisch, H; Fuess, S; Funakoshi, Y; Galloni, C; Garbincius, P H; Garcia-Bellido, A; García-González, J A; Garfinkel, A F; Garosi, P; Gavrilov, V; Geng, W; Gerber, C E; Gerberich, H; Gerchtein, E; Gershtein, Y; Giagu, S; Giakoumopoulou, V; Gibson, K; Ginsburg, C M; Ginther, G; Giokaris, N; Giromini, P; Glagolev, V; Glenzinski, D; Gogota, O; Gold, M; Goldin, D; Golossanov, A; Golovanov, G; Gomez, G; Gomez-Ceballos, G; Goncharov, M; González López, O; Gorelov, I; Goshaw, A T; Goulianos, K; Gramellini, E; Grannis, P D; Greder, S; Greenlee, H; Grenier, G; Gris, Ph; Grivaz, J-F; Grohsjean, A; Grosso-Pilcher, C; Group, R C; Grünendahl, S; Grünewald, M W; Guillemin, T; Guimaraes da Costa, J; Gutierrez, G; Gutierrez, P; Hahn, S R; Haley, J; Han, J Y; Han, L; Happacher, F; Hara, K; Harder, K; Hare, M; Harel, A; Harr, R F; Harrington-Taber, T; Hatakeyama, K; Hauptman, J M; Hays, C; Hays, J; Head, T; Hebbeker, T; Hedin, D; Hegab, H; Heinrich, J; Heinson, A P; Heintz, U; Hensel, C; Heredia-De La Cruz, I; Herndon, M; Herner, K; Hesketh, G; Hildreth, M D; Hirosky, R; Hoang, T; Hobbs, J D; Hocker, A; Hoeneisen, B; Hogan, J; Hohlfeld, M; Holzbauer, J L; Hong, Z; Hopkins, W; Hou, S; Howley, I; Hubacek, Z; Hughes, R E; Husemann, U; Hussein, M; Huston, J; Hynek, V; Iashvili, I; Ilchenko, Y; Illingworth, R; Introzzi, G; Iori, M; Ito, A S; Ivanov, A; Jabeen, S; Jaffré, M; James, E; Jang, D; Jayasinghe, A; Jayatilaka, B; Jeon, E J; Jeong, M S; Jesik, R; Jiang, P; Jindariani, S; Johns, K; Johnson, E; Johnson, M; Jonckheere, A; Jones, M; Jonsson, P; Joo, K K; Joshi, J; Jun, S Y; Jung, A W; Junk, T R; Juste, A; Kajfasz, E; Kambeitz, M; Kamon, T; Karchin, P E; Karmanov, D; Kasmi, A; Kato, Y; Katsanos, I; Kaur, M; Kehoe, R; Kermiche, S; Ketchum, W; Keung, J; Khalatyan, N; Khanov, A; Kharchilava, A; Kharzheev, Y N; Kilminster, B; Kim, D H; Kim, H S; Kim, J E; Kim, M J; Kim, S H; Kim, S B; Kim, Y J; Kim, Y K; Kimura, N; Kirby, M; Kiselevich, I; Knoepfel, K; Kohli, J M; Kondo, K; Kong, D J; Konigsberg, J; Kotwal, A V; Kozelov, A V; Kraus, J; Kreps, M; Kroll, J; Kruse, M; Kuhr, T; Kumar, A; Kupco, A; Kurata, M; Kurča, T; Kuzmin, V A; Laasanen, A T; Lammel, S; Lammers, S; Lancaster, M; Lannon, K; Latino, G; Lebrun, P; Lee, H S; Lee, H S; Lee, J S; Lee, S W; Lee, W M; Lei, X; Lellouch, J; Leo, S; Leone, S; Lewis, J D; Li, D; Li, H; Li, L; Li, Q Z; Lim, J K; Limosani, A; Lincoln, D; Linnemann, J; Lipaev, V V; Lipeles, E; Lipton, R; Lister, A; Liu, H; Liu, H; Liu, Q; Liu, T; Liu, Y; Lobodenko, A; Lockwitz, S; Loginov, A; Lokajicek, M; Lopes de Sa, R; Lucchesi, D; Lucà, A; Lueck, J; Lujan, P; Lukens, P; Luna-Garcia, R; Lungu, G; Lyon, A L; Lys, J; Lysak, R; Maciel, A K A; Madar, R; Madrak, R; Maestro, P; Magaña-Villalba, R; Malik, S; Malik, S; Malyshev, V L; Manca, G; Manousakis-Katsikakis, A; Mansour, J; Marchese, L; Margaroli, F; Marino, P; Martínez-Ortega, J; Matera, K; Mattson, M E; Mazzacane, A; Mazzanti, P; McCarthy, R; McGivern, C L; McNulty, R; Mehta, A; Mehtala, P; Meijer, M M; Melnitchouk, A; Menezes, D; Mercadante, P G; Merkin, M; Mesropian, C; Meyer, A; Meyer, J; Miao, T; Miconi, F; Mietlicki, D; Mitra, A; Miyake, H; Moed, S; Moggi, N; Mondal, N K; Moon, C S; Moore, R; Morello, M J; Mukherjee, A; Mulhearn, M; Muller, Th; Murat, P; Mussini, M; Nachtman, J; Nagai, Y; Naganoma, J; Nagy, E; Nakano, I; Napier, A; Narain, M; Nayyar, R; Neal, H A; Negret, J P; Nett, J; Neu, C; Neustroev, P; Nguyen, H T; Nigmanov, T; Nodulman, L; Noh, S Y; Norniella, O; Nunnemann, T; Oakes, L; Oh, S H; Oh, Y D; Oksuzian, I; Okusawa, T; Orava, R; Orduna, J; Ortolan, L; Osman, N; Osta, J; Pagliarone, C; Pal, A; Palencia, E; Palni, P; Papadimitriou, V; Parashar, N; Parihar, V; Park, S K; Parker, W; Partridge, R; Parua, N; Patwa, A; Pauletta, G; Paulini, M; Paus, C; Penning, B; Perfilov, M; Peters, Y; Petridis, K; Petrillo, G; Pétroff, P; Phillips, T J; Piacentino, G; Pianori, E; Pilot, J; Pitts, K; Plager, C; Pleier, M-A; Podstavkov, V M; Pondrom, L; Popov, A V; Poprocki, S; Potamianos, K; Pranko, A; Prewitt, M; Price, D; Prokopenko, N; Prokoshin, F; Ptohos, F; Punzi, G; Qian, J; Quadt, A; Quinn, B; Ratoff, P N; Razumov, I; Redondo Fernández, I; Renton, P; Rescigno, M; Rimondi, F; Ripp-Baudot, I; Ristori, L; Rizatdinova, F; Robson, A; Rodriguez, T; Rolli, S; Rominsky, M; Ronzani, M; Roser, R; Rosner, J L; Ross, A; Royon, C; Rubinov, P; Ruchti, R; Ruffini, F; Ruiz, A; Russ, J; Rusu, V; Sajot, G; Sakumoto, W K; Sakurai, Y; Sánchez-Hernández, A; Sanders, M P; Santi, L; Santos, A S; Sato, K; Savage, G; Saveliev, V; Savitskyi, M; Savoy-Navarro, A; Sawyer, L; Scanlon, T; Schamberger, R D; Scheglov, Y; Schellman, H; Schlabach, P; Schmidt, E E; Schwanenberger, C; Schwarz, T; Schwienhorst, R; Scodellaro, L; Scuri, F; Seidel, S; Seiya, Y; Sekaric, J; Semenov, A; Severini, H; Sforza, F; Shabalina, E; Shalhout, S Z; Shary, V; Shaw, S; Shchukin, A A; Shears, T; Shepard, P F; Shimojima, M; Shochet, M; Shreyber-Tecker, I; Simak, V; Simonenko, A; Skubic, P; Slattery, P; Sliwa, K; Smirnov, D; Smith, J R; Snider, F D; Snow, G R; Snow, J; Snyder, S; Söldner-Rembold, S; Song, H; Sonnenschein, L; Sorin, V; Soustruznik, K; St Denis, R; Stancari, M; Stark, J; Stentz, D; Stoyanova, D A; Strauss, M; Strologas, J; Sudo, Y; Sukhanov, A; Suslov, I; Suter, L; Svoisky, P; Takemasa, K; Takeuchi, Y; Tang, J; Tecchio, M; Teng, P K; Thom, J; Thomson, E; Thukral, V; Titov, M; Toback, D; Tokar, S; Tokmenin, V V; Tollefson, K; Tomura, T; Tonelli, D; Torre, S; Torretta, D; Totaro, P; Trovato, M; Tsai, Y-T; Tsybychev, D; Tuchming, B; Tully, C; Ukegawa, F; Uozumi, S; Uvarov, L; Uvarov, S; Uzunyan, S; Van Kooten, R; van Leeuwen, W M; Varelas, N; Varnes, E W; Vasilyev, I A; Vázquez, F; Velev, G; Vellidis, C; Verkheev, A Y; Vernieri, C; Vertogradov, L S; Verzocchi, M; Vesterinen, M; Vidal, M; Vilanova, D; Vilar, R; Vizán, J; Vogel, M; Vokac, P; Volpi, G; Wagner, P; Wahl, H D; Wallny, R; Wang, M H L S; Wang, S M; Warchol, J; Waters, D; Watts, G; Wayne, M; Weichert, J; Welty-Rieger, L; Wester, W C; Whiteson, D; Wicklund, A B; Wilbur, S; Williams, H H; Williams, M R J; Wilson, G W; Wilson, J S; Wilson, P; Winer, B L; Wittich, P; Wobisch, M; Wolbers, S; Wolfe, H; Wood, D R; Wright, T; Wu, X; Wu, Z; Wyatt, T R; Xie, Y; Yamada, R; Yamamoto, K; Yamato, D; Yang, S; Yang, T; Yang, U K; Yang, Y C; Yao, W-M; Yasuda, T; Yatsunenko, Y A; Ye, W; Ye, Z; Yeh, G P; Yi, K; Yin, H; Yip, K; Yoh, J; Yorita, K; Yoshida, T; Youn, S W; Yu, G B; Yu, I; Yu, J M; Zanetti, A M; Zeng, Y; Zennamo, J; Zhao, T G; Zhou, B; Zhou, C; Zhu, J; Zielinski, M; Zieminska, D; Zivkovic, L; Zucchelli, S

    2015-10-09

    We present the final combination of CDF and D0 measurements of cross sections for single-top-quark production in proton-antiproton collisions at a center-of-mass energy of 1.96 TeV. The data correspond to total integrated luminosities of up to 9.7 fb^{-1} per experiment. The t-channel cross section is measured to be σ_{t}=2.25_{-0.31}^{+0.29} pb. We also present the combinations of the two-dimensional measurements of the s- vs t-channel cross section. In addition, we give the combination of the s+t channel cross section measurement resulting in σ_{s+t}=3.30_{-0.40}^{+0.52} pb, without assuming the standard model value for the ratio σ_{s}/σ_{t}. The resulting value of the magnitude of the top-to-bottom quark coupling is |V_{tb}|=1.02_{-0.05}^{+0.06}, corresponding to |V_{tb}|>0.92 at the 95% C.L.

  11. Tevatron combination of single-top-quark cross sections and determination of the magnitude of the Cabibbo-Kobayashi-Maskawa matrix element $\\bf V_{tb}$

    SciTech Connect

    Aaltonen, Timo Antero

    2015-10-07

    In this study, we present the final combination of CDF and D0 measurements of cross sections for single-top-quark production in proton-antiproton collisions at a center-of-mass energy of 1.96 TeV. The data correspond to total integrated luminosities of up to 9.7 fb-1 per experiment. The t-channel cross section is measured to be σt= 2.25-0.31+0.29 pb. We also present the combinations of the two-dimensional measurements of the s- vs t-channel cross section. In addition, we give the combination of the s+t channel cross section measurement resulting in σs+t= 3.30-0.40+0.52 pb, without assuming the standard model value for the ratio σst. The resulting value of the magnitude of the top-to-bottom quark coupling is |Vtb|= 1.02-0.05+0.06, corresponding to |Vtb| > 0.92 at the 95% C.L.

  12. Whitehead Groups of Spinor Groups

    NASA Astrophysics Data System (ADS)

    Monastyrnyĭ, A. P.; Yanchevskiĭ, V. I.

    1991-02-01

    The Whitehead groups of spinor groups are studied. The known Kneser-Tits conjecture for spinor groups is reduced to a spinor analogue of the Tannaka-Artin problem, namely, to the question of whether the group K1Spin(D), where D is a division ring of exponent 2 , is trivial. A counterexample to the Kneser-Tits problem is constructed in the class of spinor groups. The group K1Spin(D) is computed. The stability of the Whitehead groups of spinor groups under purely transcendental extensions of the ground field is established. The R-equivalence on the k-points of spinor groups and the weak approximation problem are considered. The study of spinor group completes the study of the Whitehead groups of algebraic groups of classical type, that was started in studying reduced K-theory (V.P. Platonov) and was continued for reduced unitary K-theory (V.I. Yanchevskiĭ) and Hermitian K-theory (Platonov and Yanchevskiĭ). Bibliography: 50 titles.

  13. Mechanical Properties of Low-Density, Refractory Multi-Principal Element Alloys of the Cr-Nb-Ti-V-Zr System (Postprint)

    DTIC Science & Technology

    2014-04-01

    of high temperature properties, including reduced density, superior to existing Ni base superalloys or refractory alloys . Recently a high entropy ...CrMo0.5NbTa0.5TiZr [8,9]. The first three alloys are single phase with a BCC crystal structure, probably due to high entropy of mixing and similar atomic radii of...design strategies used to predict stable high entropy alloys suggest [10,11] that this is the result of adding an element, Cr, which has a much

  14. The elemental abundances in interplanetary dust particles

    NASA Astrophysics Data System (ADS)

    Arndt, Peter; Bohsung, Jörg; Maetz, Mischa; Jessberger, Elmar K.

    1996-11-01

    We compiled a table of all major, minor, and trace-element abundances in 89 interplanetary dust particles (IDPs) that includes data obtained with proton-induced x-ray emission (PIXE), synchroton x-ray fluorescence (SXRF), and secondary ion mass spectrometry (SIMS). For the first time, the reliability of the trace-element abundances in IDPs is tested by various crosschecks. We also report on the results of cluster analyses that we performed on IDP compositions. Because of the incompleteness of the data set, we included only the elements Cr, Mn, Ni, Cu, and Zn, normalized to Fe and CI chondrite abundances, that are determined in 73 IDPs. The data arrange themselves in four rather poorly defined groups that we discuss in relation to CI chondrites following the assumption that on the average CI abundances are most probable. The largest group (chondritic), with 44 members, has close to CI abundances for many refractory and moderately refractory elements (Na, Al, Si, P, K, Sc, Ti, V, Cr, Co, Ge, Sr). It is slightly depleted in Fe and more in Ca and S, while the volatile elements (Cl, Cu, Zn, Ga, Se, Rb) are enriched by =1.7 × CI and Br by 21 × CI. The low-Zn group, with 12 members, is very similar to the chondritic group except for its Zn-depletion, stronger Ca-depletion and Fe-enrichment. The low-Ni group, with 11 members, has Ni/Fe = 0.03 × CI and almost CI-like Ca, but its extraterrestrial origin is not established. The last group (6 members) contains non-systematic particles of unknown origin. We found that Fe is inhomogeneously distributed on a micron scale. Furthermore, the abundances of elements that are measured near their limits of detection are easily overestimated. These biases involved, the incomplete data set and possible contaminating processes prevent us from obtaining information on the specific origin(s) of IDPs from elemental abundances.

  15. Synthesis and characterization of some new Schiff base complexes of group 13 elements, ab initio studies, cytotoxicity and reaction with hydrogen peroxide.

    PubMed

    Asadi, Mozaffar; Savaripoor, Nooshin; Asadi, Zahra; Ghatee, Mohammad Hadi; Moosavi, Fatemeh; Yousefi, Reza; Jamshidi, Mehrnaz

    2013-01-15

    A novel tetradentate Schiff base, naphthabza-H2=N,N'-bis(naphthylidene)-2-aminobenzylamine, and a series of aluminum(III), gallium(III), and indium(III) complexes with general formula, MLNO3, were synthesized and characterized by elemental analysis, 1H NMR, FT-IR, UV-Vis spectroscopy and thermogravimetric method. The product of the reaction of complexes with hydrogen peroxide was characterized by similar techniques. According to the ab initio calculations aluminum and gallium complexes have five-coordinated structures and indium complex is a six-coordinated one. Also, the growth inhibitory effects of the complexes toward K562 cancer cell line were measured and the results for these complexes are as follows: Al>Ga>In.

  16. Evaluation of essential trace and toxic elements in biological samples of normal and night blindness children of age groups 3-7 and 8-12 years.

    PubMed

    Afridi, Hassan Imran; Kazi, Tasneem Gul; Kazi, Naveed; Kandhro, Ghulam Abbas; Baig, Jameel Ahmed; Shah, Abdul Qadir; Wadhwa, Sham Kumar; Khan, Sumaira; Kolachi, Nida Fatima; Shah, Faheem; Jamali, Mohammad Khan; Arain, Mohammad Balal; Sirajuddin

    2011-10-01

    The most common cause of blindness in developing countries is vitamin A deficiency. The World Health Organization estimates 13.8 million children to have some degree of visual loss related to vitamin A deficiency. The causes of night blindness in children are multifactorial, and particular consideration has been given to childhood nutritional deficiency, which is the most common problem found in underdeveloped countries. Such deficiency can result in physiological and pathological processes that in turn influence biological samples composition. Vitamin and mineral deficiency prevents more than two billion people from achieving their full intellectual and physical potential. This study was designed to compare the levels of Zn, Mg, Ca, K, Na, As, Cd, and Pb in scalp hair, blood, and urine of night blindness children age ranged 3-7 and 8-12 years of both genders, comparing them to sex- and age-matched controls. A microwave-assisted wet acid digestion procedure was developed as a sample pretreatment, for the determination of As, Ca, Cd, K, Pb, Mg, Na, and Zn in biological samples of night blindness children. The proposed method was validated by using conventional wet digestion and certified reference samples of hair, blood, and urine. The concentrations of trace and toxic elements were measured by atomic absorption spectrophotometer prior to microwave-assisted acid digestion. The results of this study showed that the mean values of As, Cd, Na, and Pb were significantly higher in scalp hair, blood, and urine samples of male and female night blindness children than in referents (p < 0.001), whereas the concentrations of Zn, Ca, K, and Mg were lower in the scalp hair and blood but higher in the urine samples of night blindness children. These data present guidance to clinicians and other professional investigating deficiency of essential mineral elements in biological samples (scalp hair and blood) of night blindness children.

  17. Practical Application of Finite Element Analysis to Aircraft Structural Design

    DTIC Science & Technology

    1986-08-01

    t] Cook, Robert D., "Concepts and Applications of Finite element Analysis," John Wiley & Sons, Inc., New York, 1981. [5] Rao, S. S., "The Finite...generation large-scale computer programs is discussed. V.P. Analysis of aircraft structure using applied fracture mechanics (AA) WILHEM , D. P. Northrop...Analytical, finite element for surface flaws, holes (AA) WILHEM , D. P. Northrop Corp., Hawthorne, Calif. (N5631231) Aircraft Group. In AGARD Fracture

  18. Value of the Kobayashi-Maskawa-Cabibbo matrix element V sub u s and flavor-symmetry breaking in hyperon semileptonic decays

    SciTech Connect

    Garcia, A.; Huerta, R.; Kielanowski, P. )

    1992-02-01

    We perform a detailed model-independent analysis of the determination of {ital V}{sub {ital u}{ital s}} in the {Delta}{ital S}=1 decays {Lambda}{r arrow}{ital pe}{nu}, {Sigma}{sup {minus}}{r arrow}{ital ne}{nu}, and {Xi}{sup {minus}}{r arrow}{Lambda}{ital e}{nu}. Values systematically higher than the {ital K}{sub {ital e}3} one are obtained. A reconciliation may be only obtained through second-order changes of a few percent in the leading vector form factors {ital f}{sub 1}, provided that these changes always increase their magnitudes over their conserved vector current (CVC) predictions. Using the CVC or the recoil part of recent flavor-symmetry-breaking calculations, the value {ital V}{sub {ital u}{ital s}}=0.2258{plus minus}0.0027 is obtained, which is higher than the {ital K}{sub {ital e}3} one by 2.6 standard deviations.

  19. Solar cosmic ray composition above 10 MeV/nucleon and its energy dependence in the 4 August 1972 event. [including proton, helium, and Fe-group nuclei fluxes

    NASA Technical Reports Server (NTRS)

    Bertsch, D. L.; Biswas, S.; Reames, D. V.

    1974-01-01

    Observations of the proton, helium (C,N,O) and Fe-group nuclei fluxes made during the large 4 August 1972 solar particle event are presented. The results show a small, but significant variation of the composition of multicharged nuclei as a function of energy in the energy region above 10 MeV/nucleon. In particular, the He/(C,N,O) abundance ratio varies by a factor approximately 2 between 10 and 50 MeV/nucleon, and the Fe-group/(C,N,O) ratio suggests a similar variation. Abundance ratios from the 4 August 1972 event are compared as a function of energy with ratios measured in other solar events. At energies approximately greater than 50 MeV/nucleon, the He/(C,N,O) abundance ratio for August 1972 is consistent with all earlier measurements made above that energy.

  20. Effects of long-lived 10 MeV-scale sterile neutrinos on primordial elemental abundances and the effective neutrino number

    NASA Astrophysics Data System (ADS)

    Ishida, Hiroyuki; Kusakabe, Motohiko; Okada, Hiroshi

    2014-10-01

    The primordial lithium abundance inferred from spectroscopic observations of metal-poor stars is ˜3 times smaller than the theoretical prediction in the standard big bang nucleosynthesis (BBN) model. We assume a simple model composed of standard model particles and a sterile neutrino νH with mass of O(10) MeV which decays long after BBN. We then investigate cosmological effects of a sterile neutrino decay, and check if a sterile neutrino can reduce the primordial lithium abundance. We formulate the injection spectrum of nonthermal photon induced by the νH decay. We take into account the generation of electrons and positrons, e±'s, and active neutrinos at the νH decay, the primary photon production via the inverse Compton scattering of cosmic background radiation (CBR) by energetic e±, and electromagnetic cascade showers induced by the primary photons. The steady state injection spectrum is then derived as a function of the νH mass and the photon temperature. The νH decay produces energetic active neutrinos which are not thermalized, and e±'s which are thermalized. We then derive formulas relevant to the νH decay rates and formulas for the baryon-to-photon ratio η and effective neutrino number Neff. The initial abundance, mass, and lifetime of νH are taken as free parameters. We then consistently solve (1) the cosmic thermal history, (2) nonthermal nucleosynthesis induced by the nonthermal photons, (3) the η value, and (4) the Neff value. We find that an effective Be7 destruction can occur only if the sterile neutrino decays at photon temperature T =O(1) keV. Amounts of energy injection at the νH decay are constrained from limits on primordial D and Li7 abundances, the Neff value, and the CBR energy spectrum. We find that Be7 is photodisintegrated and the Li problem is partially solved for the lifetime 104-105 s and the mass ≳14 MeV. Be7 destruction by more than a factor of 3 is not possible because of an associated D overdestruction. In the

  1. NASA Constellation Program (CxP) Key Driving Requirements and Element Descriptions for International Architecture Working Group (IAWG) Functional Teams Human Transportation Cargo Transportation

    NASA Technical Reports Server (NTRS)

    Martinez, Roland M.

    2009-01-01

    The NASA Constellation uncrewed cargo mission delivers cargo to any designated location on the lunar surface (or other staging point) in a single mission. This capability is used to deliver surface infrastructure needed for lunar outpost construction, to provide periodic logistics resupply to support a continuous human lunar presence, and potentially deliver other assets to various locations.In the nominal mission mode, the Altair lunar lander is launched on Ares V into Low Earth Orbit (LEO), following a short Low Earth Orbit (LEO) loiter period, the Earth Departure Stage (EDS) performs the Trans Lunar Injection (TLI) burn and is then jettisoned. The Altair performs translunar trajectory correction maneuvers as necessary and performs the Lunar Orbit Insertion (LOI) burn. Altair then descends to the surface to land near a designated target, presumably in proximity to an Outpost location or another site of interest for exploration.Alternatively, the EDS and Altair Descent Stage could deliver assets to various staging points within their propulsive capabilities.

  2. Role of vanadium (V) in the differentiation of C3H10t1/2 cells towards osteoblast lineage: a comparative analysis with other trace elements.

    PubMed

    Srivastava, Swati; Kumar, Narender; Thakur, Rajani Salunke; Roy, Partha

    2013-04-01

    In recent time, vanadium compounds are being used as antidiabetic drug and in orthopedic implants. However, the exact role of this incorporated vanadium in improving the quality of bone structure and morphology is not known. The impact of vanadium ion was studied and compared to other trace metal ions with respect to the proliferation and osteoblast differentiation of C3H10t1/2 cells. Toxicity profile of these trace metal ions revealed a descending toxicity trend of Fe(2+) > Zn(2+) > Cu(2+) > Co(2+) > Mn(2+) > V(5+) > Cr(2+). The effect of vanadium and other trace metal ions on osteoblast differentiation was evaluated by culturing the cells for 10 days in osteoblastic medium supplemented with different trace ions at concentrations lower than their cytotoxic doses. The results indicated that vanadium has maximum impact on the induction of osteoblast differentiation by upregulating alkaline phosphatase activity and mineralization by up to 145 and 150 %, respectively (p < 0.05), over control. Cu(2+) and Zn(2+) had a mild inhibitory effect, while Mn(2+), Fe(2+), and Co(2+) demonstrated a clear decrease in osteoblast differentiation when compared to the control. The data as presented here demonstrate that orthopedic implants, if supplemented with trace metals like vanadium, may provide a source of better model for bone formation and its turnover.

  3. Determination of Specific Forces and Tool Deflections in Micro-milling of Ti-6Al-4V alloy using Finite Element Simulations and Analysis

    SciTech Connect

    Farina, Simone; Ceretti, Elisabetta; Thepsonti, Thanongsak; Oezel, Tugrul

    2011-05-04

    Titanium alloys offer superb properties in strength, corrosion resistance and biocompatibility and are commonly utilized in medical devices and implants. Micro-end milling process is a direct and rapid fabrication method for manufacturing medical devices and implants in titanium alloys. Process performance and quality depend upon an understanding of the relationship between cutting parameters and forces and resultant tool deflections to avoid tool breakage. For this purpose, FE simulations of chip formation during micro-end milling of Ti-6Al-4V alloy with an ultra-fine grain solid carbide two-flute micro-end mill are investigated using DEFORM software.At first, specific forces in tangential and radial directions of cutting during micro-end milling for varying feed advance and rotational speeds have been determined using designed FE simulations for chip formation process. Later, these forces are applied to the micro-end mill geometry along the axial depth of cut in 3D analysis of ABAQUS. Consequently, 3D distributions for tool deflections and von Misses stress are determined. These analyses will yield in establishing integrated multi-physics process models for high performance micro-end milling and a leap-forward to process improvements.

  4. Measurement of the Electroweak Single Top Quark Production Cross Section and the CKM Matrix Element $|V_{tb}|$ at CDF Run II

    SciTech Connect

    Larana, Bruno Casal

    2010-01-01

    The establishment of the electroweak single top quark production at CDF is experimentally challenging. The small single top signal hidden under large uncertain background processes makes it necessary an excellent understanding of the detector and a detailed study of the processes involved. Moreover, simple counting experiments are not sufficient to extract enough information from the candidate event sample and multivariate analysis techniques are crucial to distinguish signal from background. This thesis presents the world’s most sensitive individual search, together with CDF’s Neural Network analysis, for the combined s- and t-channel single top production. This analysis uses a dataset that corresponds to an integrated luminosity of 3.2fb-1, and is based on a Boosted Decision Tree method that combines information from several input variables to construct a final powerful discriminant, reaching a sensitivity to the combined single top quark production equivalent to 5.2σ. The measured combined single top quark production cross section is 2.1+0.7 -0.6 pb assuming a top quark mass of 175 GeV/c2. The probability that this result comes from a background-only fluctuation (p-value) is 0.0002, which corresponds to 3.5σ.

  5. Tevatron combination of single-top-quark cross sections and determination of the magnitude of the Cabibbo-Kobayashi-Maskawa matrix element $$\\bf V_{tb}$$

    DOE PAGES

    Aaltonen, Timo Antero; Helsinki Institute of Physics, Helsinki

    2015-10-07

    In this study, we present the final combination of CDF and D0 measurements of cross sections for single-top-quark production in proton-antiproton collisions at a center-of-mass energy of 1.96 TeV. The data correspond to total integrated luminosities of up to 9.7 fb-1 per experiment. The t-channel cross section is measured to be σt= 2.25-0.31+0.29 pb. We also present the combinations of the two-dimensional measurements of the s- vs t-channel cross section. In addition, we give the combination of the s+t channel cross section measurement resulting in σs+t= 3.30-0.40+0.52 pb, without assuming the standard model value for the ratio σs/σt. The resulting valuemore » of the magnitude of the top-to-bottom quark coupling is |Vtb|= 1.02-0.05+0.06, corresponding to |Vtb| > 0.92 at the 95% C.L.« less

  6. OCO and NCO chelated derivatives of heavier group 15 elements. Study on possibility of cyclization reaction via intramolecular ether bond cleavage.

    PubMed

    Dostál, Libor; Jambor, Roman; Růžička, Aleš; Jirásko, Robert; Holeček, Jaroslav; De Proft, Frank

    2011-09-21

    A set of four pincer ligands, either the OCO type ligands L(1-3) [2,6-(ROCH(2))(2)C(6)H(3)](-), where R = Me (L(1)), mesityl (L(2)), t-Bu (L(3)) or novel NCO ligand [2-(Me(2)NCH(2))-6-(t-BuOCH(2))C(6)H(3)](-) was studied. The reaction of L(4)Li with PCl(3) resulted in isolation of [2-(OCH(2))-6-(Me(2)NCH(2))C(6)H(3)]PCl (1) as a result of intramolecular ether bond cleavage and elimination of t-BuCl. The conversion between the organolithium compounds L(1,2,4)Li and AsCl(3) led to the desired chlorides, i.e. (L(1))(2)AsCl (2), L(2)AsCl(2) (3), L(4)AsCl(2) (5), but an analogous reaction using the L(3)Li compound gave [2-(OCH(2))-6-(t-BuOCH(2))C(6)H(3)]AsCl (4) as a result of intramolecular cyclization. The organoantimony chloride L(3)SbCl(2) was shown to undergo very slow cyclization in CDCl(3) again via elimination of t-BuCl giving [2-(OCH(2))-6-(t-BuOCH(2))C(6)H(3)]SbCl (6) and it was demonstrated that this reaction may be accelerated by preparation of L(3)Sb(Cl)(OTf) (7) with more Lewis acidic central atom. On the contrary, both antimony derivatives of the NCO ligand L(4), not only the chloride L(4)SbCl(2) (8) but also the ionic pair containing highly Lewis acidic cation [L(4)SbCl](+)[CB(11)H(12)](-) (9), are stable without any indication for etheral bond cleavage. The situation is rather similar in the case of organobismuth derivatives of L(4), which allowed isolation of compounds L(4)BiCl(2) (10), L(4)Bi(Cl)(OTf) (11) and [L(4)BiCl](+)[CB(11)H(12)](-) (12). All studied compounds were characterized by the help of (1)H and (13)C NMR spectroscopy, ESI mass spectrometry, elemental analysis and (except 1) by single-crystal X-ray diffraction.

  7. Geochemistry of trace elements in coals from the Zhuji Mine, Huainan Coalfield, Anhui, China

    USGS Publications Warehouse

    Sun, R.; Liu, Gaisheng; Zheng, Lingyun; Chou, C.-L.

    2010-01-01

    The abundances of nine major elements and thirty-eight trace elements in 520 samples of low sulfur coals from the Zhuji Mine, Huainan Coalfield, Anhui, China, were determined. Samples were mainly collected from 10 minable coal seams of 29 boreholes during exploration. The B content in coals shows that the influence of brackish water decreased toward the top of coal seams; marine transgression and regression occurred frequently in the Lower Shihezi Formation. A wide range of elemental abundances is found. Weighted means of Na, K, Fe, P, Be, B, Co, Ni, Cr, Se, Sb, Ba, and Bi abundances in Zhuji coals are higher, and the remainder elements are either lower or equal to the average values of elements in coals of northern China. Compared to the Chinese coals, the Zhuji coals are higher in Na, K, Be, B, Cr, Co, Se, Sn, Sb, and Bi, but lower in Ti, P, Li, V and Zn. The Zhuji coals are lower only in S, P, V and Zn than average U.S. and world coals. Potassium, Mg, Ca, Mn, Sr, As, Se, Sb and light rare earth elements (LREE) had a tendency to be enriched in thicker coal seams, whereas Fe, Ti, P, V, Co, Ni, Y, Mo, Pb and heavy rare earth elements (HREE) were inclined to concentrate in thinner coal seams. The enrichment of some elements in the Shanxi or Upper Shihezi Formations is related to their depositional environments. The elements are classified into three groups based on their stratigraphic distributions from coal seams 3 to 11-2, and the characteristics of each group are discussed. Lateral distributions of selected elements are also investigated. The correlation coefficients of elemental abundances with ash content show that the elements may be classified into four groups related to modes of occurrence of these elements. ?? 2009 Elsevier B.V. All rights reserved.

  8. [Distribution of chemical elements in whole blood and plasma].

    PubMed

    Barashkov, G K; Zaĭtseva, L I; Kondakhchan, M A; Konstantinova, E A

    2003-01-01

    The distribution factor (Fd) of 35 elements of plasma and whole blood in 26 healthy men and women was detected by ICP-OES. Usilig this parameter the elements were subdivided in 3 pools. 9 of them have Fd higher than 1.5 ("elements of plasma"-Ag, Ca, Cu, In, Li, Na, Se, Si, Sr); 6 have lower than 0.5 ("elements of blood cells"-Fe, K, Mn, Ni, V, Zn), other 20-about 1 ("blood elements"). Fd of all elements depends on ionic radius. Elements of 2nd sub-groups of all groups of Mendeleev's periodic table ("heavy metals") depend on the similar law: "with growing of ionic radius the concentration of elements in plasma enhances". In alkaline metals Fd depends on the opposite law:" with growing of ionic radius of alkaline metal the quantity of elements in blood cells enhance". Dependence of Fd on the value of atomic mass in periods or in exterior electronic cloud (s-, p-, d-, f-) was not established. The table of distribution of all detected elements in whole blood in relation to 8 macroelements (Ca, Mg, K, Na, S, P, Fe, Zn,) is presented, as a basic diagnostic criteria in metal-ligand homeostasis disturbance.

  9. Group typicality, group loyalty and cognitive development.

    PubMed

    Patterson, Meagan M

    2014-09-01

    Over the course of childhood, children's thinking about social groups changes in a variety of ways. Developmental Subjective Group Dynamics (DSGD) theory emphasizes children's understanding of the importance of conforming to group norms. Abrams et al.'s study, which uses DSGD theory as a framework, demonstrates the social cognitive skills underlying young elementary school children's thinking about group norms. Future research on children's thinking about groups and group norms should explore additional elements of this topic, including aspects of typicality beyond loyalty.

  10. Hydroxypyridinonate complex stability of group (IV) metals and tetravalent f-block elements: the key to the next generation of chelating agents for radiopharmaceuticals.

    PubMed

    Sturzbecher-Hoehne, Manuel; Choi, Taylor A; Abergel, Rebecca J

    2015-04-06

    The solution thermodynamics of the water-soluble complexes formed between 3,4,3-LI(1,2-HOPO) and Zr(IV) or Pu(IV) were investigated to establish the metal coordination properties of this octadentate chelating agent. Stability constants log β110 = 43.1 ± 0.6 and 43.5 ± 0.7 were determined for [Zr(IV)(3,4,3-LI(1,2-HOPO))] and [Pu(IV)(3,4,3-LI(1,2-HOPO))], respectively, by spectrophotometric competition titrations against Ce(IV). Such high thermodynamic stabilities not only confirm the unparalleled Pu(IV) affinity of 3,4,3-LI(1,2-HOPO) as a decorporation agent but also corroborate the great potential of hydroxypyridinonate ligands as new (89)Zr-chelating platforms for immuno-PET applications. These experimental values are in excellent agreement with previous estimates and are discussed with respect to ionic radius and electronic configuration, in comparison with those of Ce(IV) and Th(IV). Furthermore, a liquid chromatography assay combined with mass spectrometric detection was developed to probe the separation of the neutral [M(IV)(3,4,3-LI(1,2-HOPO))] complex species (M = Zr, Ce, Th, and Pu), providing additional insight into the coordination differences between group IV and tetravalent f-block metals and on the role of d and f orbitals in bonding interactions.

  11. Explanation and elaboration of the SQUIRE (Standards for Quality Improvement Reporting Excellence) Guidelines, V.2.0: examples of SQUIRE elements in the healthcare improvement literature

    PubMed Central

    Goodman, Daisy; Ogrinc, Greg; Davies, Louise; Baker, G Ross; Barnsteiner, Jane; Foster, Tina C; Gali, Kari; Hilden, Joanne; Horwitz, Leora; Kaplan, Heather C; Leis, Jerome; Matulis, John C; Michie, Susan; Miltner, Rebecca; Neily, Julia; Nelson, William A; Niedner, Matthew; Oliver, Brant; Rutman, Lori; Thomson, Richard

    2016-01-01

    Since its publication in 2008, SQUIRE (Standards for Quality Improvement Reporting Excellence) has contributed to the completeness and transparency of reporting of quality improvement work, providing guidance to authors and reviewers of reports on healthcare improvement work. In the interim, enormous growth has occurred in understanding factors that influence the success, and failure, of healthcare improvement efforts. Progress has been particularly strong in three areas: the understanding of the theoretical basis for improvement work; the impact of contextual factors on outcomes; and the development of methodologies for studying improvement work. Consequently, there is now a need to revise the original publication guidelines. To reflect the breadth of knowledge and experience in the field, we solicited input from a wide variety of authors, editors and improvement professionals during the guideline revision process. This Explanation and Elaboration document (E&E) is a companion to the revised SQUIRE guidelines, SQUIRE 2.0. The product of collaboration by an international and interprofessional group of authors, this document provides examples from the published literature, and an explanation of how each reflects the intent of a specific item in SQUIRE. The purpose of the guidelines is to assist authors in writing clearly, precisely and completely about systematic efforts to improve the quality, safety and value of healthcare services. Authors can explore the SQUIRE statement, this E&E and related documents in detail at http://www.squire-statement.org. PMID:27076505

  12. Randomized Phase III Trial of ABVD Versus Stanford V With or Without Radiation Therapy in Locally Extensive and Advanced-Stage Hodgkin Lymphoma: An Intergroup Study Coordinated by the Eastern Cooperative Oncology Group (E2496)

    PubMed Central

    Gordon, Leo I.; Hong, Fangxin; Fisher, Richard I.; Bartlett, Nancy L.; Connors, Joseph M.; Gascoyne, Randy D.; Wagner, Henry; Stiff, Patrick J.; Cheson, Bruce D.; Gospodarowicz, Mary; Advani, Ranjana; Kahl, Brad S.; Friedberg, Jonathan W.; Blum, Kristie A.; Habermann, Thomas M.; Tuscano, Joseph M.; Hoppe, Richard T.; Horning, Sandra J.

    2013-01-01

    Purpose Although ABVD (doxorubicin, bleomycin, vinblastine, and dacarbazine) has been established as the standard of care in patients with advanced Hodgkin lymphoma, newer regimens have been investigated, which have appeared superior in early phase II studies. Our aim was to determine if failure-free survival was superior in patients treated with the Stanford V regimen compared with ABVD. Patients and Methods The Eastern Cooperative Oncology Group, along with the Cancer and Leukemia Group B, the Southwest Oncology Group, and the Canadian NCIC Clinical Trials Group, conducted this randomized phase III trial in patients with advanced Hodgkin lymphoma. Stratification factors included extent of disease (localized v extensive) and International Prognostic Factors Project Score (0 to 2 v 3 to 7). The primary end point was failure-free survival (FFS), defined as the time from random assignment to progression, relapse, or death, whichever occurred first. Overall survival, a secondary end point, was measured from random assignment to death as a result of any cause. This design provided 87% power to detect a 33% reduction in FFS hazard rate, or a difference in 5-year FFS of 64% versus 74% at two-sided .05 significance level. Results There was no significant difference in the overall response rate between the two arms, with complete remission and clinical complete remission rates of 73% for ABVD and 69% for Stanford V. At a median follow-up of 6.4 years, there was no difference in FFS: 74% for ABVD and 71% for Stanford V at 5 years (P = .32). Conclusion ABVD remains the standard of care for patients with advanced Hodgkin lymphoma. PMID:23182987

  13. Secondary elements of blood pH variation can influence the effort effectiveness based on adaptive changes within a group of elite athletes

    PubMed Central

    MARTIN, ŞTEFAN ADRIAN; TOMESCU, VALERIU; VOIDĂZAN, SEPTIMIU

    2016-01-01

    Aim pH is the direct indicator of the body reaction following the activities performed. Establishing precise correlations between pH and blood biochemical parameters might support the balancing of values during periods of marked physical activity. Method We conducted a case study in a group of elite rowers. Twelve athletes were included in the study. Monitoring was carried out by collecting biological samples several times a day: in the morning, 80 minutes pre-workout, 12 hours after the last physical effort performed, at two different times, 10 days apart. Determinations were aimed at adapting the reported biochemical parameters depending on the effort performed. The following parameters were monitored: pH, HCO3, pCO2, pO2, BE, SBE, SBC, Ca++, Mg++, LDH, GPT, T-Pro, and Alb. Results The mean value of pH found in athletes was 7.41±0.024. The value obtained was significantly correlated to biochemical parameters such as BE (2.32±1.79), SBC (1.67±1.45), SBE (2.70±1.75). However, bicarbonate (HCO3) was statistically significantly related with SBE, SBC, SBE, and pO2, but did not present a strong association with the pH value (p=0.094). However, values such as Alb, Ca++, LDH, BE, SBC are related to pH value as a result of variations in the data submitted. Conclusions The processed data evidence the fact that blood pH, in this case, is significantly influenced by a number of indices that correlate energy system activity, individual adaptation to effort, and the recovery process. The parameters under investigation (SBE, SBC, SBE, CPK, LDH) are associated with pH changes that could confirm the recovery efficiency of the athlete, along with a possible metabolic acidosis/alkalosis. PMID:27857520

  14. The expression patterns of beta1,4 galactosyltransferase I and V mRNAs, and Galbeta1-4GlcNAc group in rat gastrocnemius muscles post sciatic nerve injury.

    PubMed

    Yan, Meijuan; Cheng, Chun; Ding, Fei; Jiang, Jing; Gao, Lingling; Xia, Chunlin; Shen, Aiguo

    2008-10-01

    Glycosylation is one of the most important post-translational modifications. It is clear that the single step of beta1,4-galactosylation is performed by a family of beta1,4-galactosyltransferases (beta1,4-GalTs), and that each member of this family may play a distinct role in different tissues and cells. beta1,4-GalT I and V are involved in the biosynthesis of N-linked oligosaccharides and play roles in sciatic nerve regeneration after sciatic nerve injury. In the present study, the expression of beta1,4-galactosyltransferase (beta1,4-GalT) I, V mRNAs and Galbeta1-4GlcNAc group were examined in rat gastrocnemius muscles after sciatic nerve crush and transection. Real time PCR revealed that beta1,4-GalT I and V mRNAs expressed at a high level in normal gastrocnemius muscles and decreased gradually from 6 h, reached the lowest level at 2 weeks, then restored gradually to relatively normal level at 4 weeks after sciatic nerve crush. In contrast, in sciatic nerve transection model, beta1,4-GalT I and V mRNAs decreased gradually from 6 h, and remained on a low level at 4 weeks in gastrocnemius muscles after sciatic nerve transection. In situ hybridization indicated that beta1,4-GalT I and V mRNAs localized in numerous myocytes and muscle satellite cells under normal conditions and at 4 weeks after sciatic nerve crush, and in a few muscle satellite cells at 4 weeks after sciatic nerve transection. Furthermore, lectin blotting showed that the expression level of the Galbeta1-4GlcNAc group decreased from 6 h, reached the lowest level at 2 weeks, and restored to relatively normal level at 4 weeks after sciatic nerve crush. RCA-I lectin histochemistry demonstrated that Galbeta1-4GlcNAc group localized in numerous membranes of myocytes and muscle satellite cells in normal and at 4 weeks after sciatic nerve crush, and in a few muscle satellite cells at 2 and 4 weeks after sciatic nerve transection. These results indicated that the expressions of beta1,4-GalT I, V mRNAs and

  15. Group separation of transplutonium and rare-earth elements by liquid chromatography with a free stationary phase using 2,4,6-Tris[ditolylphosphoryl]-1,3,5-triazine

    SciTech Connect

    Chmutova, M.K.; Ivanova, L.A.; Bodrin, G.B.

    1995-03-01

    Methods are developed for group separation of trace quantities of transplutonium (TPE) and weighable amounts of rare-earth elements (REE) by liquid chromatography with a free stationary phase in systems based on bifunctional neutral organophosphorus compounds. Using a stationary phase of 2,4,6-tris(ditolylphosphoryl)-1,3,5-triazine in CHCl{sub 3}, REE are first eluted by 0.5 M NH{sub 4}SCN-1 M HCl and then TPE by 0.025 M hydroxyethylidenediphosphonic acid in H{sub 2}O. The fractions contained {approximately} 100% of one of the groups without an impurity of the other. Use of the same eluents and a CHCl{sub 3} solution of tetraphenyl-methylenediphosphine dioxide as the stationary phase gave 95.4% pure REE and 97.5% pure TPE.

  16. Chemistry of high-oxidation-state groups V and VI complexes: Novel silyl and imido complexes and the reactions of silyl and alkyl alkylidyne complexes with oxygen

    NASA Astrophysics Data System (ADS)

    Chen, Tianniu

    This dissertation describes the synthesis and characterization of the novel early transition metal (especially group VI metals) complexes free of anionic pi-ligands such as cyclopentadienyl (Cp) and studies of their reactions with oxygen and silanes. Our study of Cp-free tungsten silyl chemistry is reported. A novel d 0 tungsten silyl complex 2 [(ButCH 2)W(=CHBut)2(SiButPh2 ) (2a) ⇌ (ButCH2)2W(≡CBu t)(SiButPh2) (2b)] and an equilibrium between 2a and 2b are described in Chapter 2. The thermodynamics of this equilibrium [DeltaH° = -0.9(0.2) kcal/mol, DeltaS° = -0.6(0.8) eu] was investigated by 1H NMR. The studies of the alpha-hydrogen exchange between 2a and 2b by 2-D EXSY experiments gave kinetic parameters of the exchange: DeltaH≠ = 17.9(1.1) kcal/mol, DeltaS≠ = 1.9(5.7) eu for the forward reaction (2a → 2b) and Delta H≠ = 18.6 (1.1) kcal/mol, DeltaS ≠ = 1.9(5.7) eu for the back reaction (2b → 2a). The reaction of O2 with silyl alkylidyne 2b [(Bu tCH2)W(=CHBut)2(SiBut Ph2) (2a) ⇌ (ButCH2)2W(≡CBu t)(SiButPh2) (2b)] is described in Chapter 3. A silyl migration product (ButCH2) 2W(=O)[=C(But)(SiButPh2)] ( 5) was characterized. A siloxy analog of 2b, (Bu tCH2)2W≡CBut(OSiBu tPh2) (6), was prepared and excluded as a possible intermediate in the formation of 5. Ab initio calculations suggested a pathway involving silyl migration in 2b to give a tungsten (IV) intermediate (ButCH 2)2W=C(But)(SiButPh2) (7) prior to the reaction with O2. A crystal structure of (Me3SiCH2)2W(=O)(=CHSiMe3)(O=PMe 3)•(Me3SiCH2)3W≡CSiMe 3 (12) was obtained from the reaction of alkyl alkylidyne (Me3SiCH2)3W≡CSiMe3 with O2 in the presence of PMe3. In Chapter 4, preparation and characterization of bis(2,6-diisopropylphenylimido)molybdenum(VI) amide and silyl complexes (ArN=)2Mo(NMe2)2 (14), (ArN=)2Mo(NMe2)[Si(SiMe3) 3] (15), (ArN=)2MoCl[N(SiMe3) 2] (16), (ArN=)2Mo(NMe2)[N(SiMe 3)2] (17), and (ArN=)2Mo(NHAr) 2 (18) are reported. In addition, new bis

  17. Search for standard model Higgs boson production in association with a W boson using a matrix element technique at CDF in pp̄ collisions at √s=1.96 TeV

    DOE PAGES

    Aaltonen, T.; Álvarez González, B.; Amerio, S.; ...

    2012-04-02

    This paper presents a search for standard model Higgs boson production in association with a W boson using events recorded by the CDF experiment in a data set corresponding to an integrated luminosity of 5.6 fb⁻¹. The search is performed using a matrix element technique in which the signal and background hypotheses are used to create a powerful discriminator. The discriminant output distributions for signal and background are fit to the observed events using a binned likelihood approach to search for the Higgs boson signal. We find no evidence for a Higgs boson, and 95% confidence level (C.L.) upper limitsmore » are set on σ(pp̄→WH)×B(H→bb¯). The observed limits range from 3.5 to 37.6 relative to the standard model expectation for Higgs boson masses between mH=100 GeV/c² and mH=150 GeV/c². The 95% C.L. expected limit is estimated from the median of an ensemble of simulated experiments and varies between 2.9 and 32.7 relative to the production rate predicted by the standard model over the Higgs boson mass range studied.« less

  18. Search for standard model Higgs boson production in association with a W boson using a matrix element technique at CDF in pp̄ collisions at √s=1.96 TeV

    SciTech Connect

    Aaltonen, T.; Álvarez González, B.; Amerio, S.; Amidei, D.; Anastassov, A.; Annovi, A.; Antos, J.; Apollinari, G.; Appel, J. A.; Arisawa, T.; Artikov, A.; Asaadi, J.; Ashmanskas, W.; Auerbach, B.; Aurisano, A.; Azfar, F.; Badgett, W.; Bae, T.; Barbaro-Galtieri, A.; Barnes, V. E.; Barnett, B. A.; Barria, P.; Bartos, P.; Bauce, M.; Bedeschi, F.; Behari, S.; Bellettini, G.; Bellinger, J.; Benjamin, D.; Beretvas, A.; Bhatti, A.; Bisello, D.; Bizjak, I.; Bland, K. R.; Blumenfeld, B.; Bocci, A.; Bodek, A.; Bortoletto, D.; Boudreau, J.; Boveia, A.; Brigliadori, L.; Bromberg, C.; Brucken, E.; Budagov, J.; Budd, H. S.; Burkett, K.; Busetto, G.; Bussey, P.; Buzatu, A.; Calamba, A.; Calancha, C.; Camarda, S.; Campanelli, M.; Campbell, M.; Canelli, F.; Carls, B.; Carlsmith, D.; Carosi, R.; Carrillo, S.; Carron, S.; Casal, B.; Casarsa, M.; Castro, A.; Catastini, P.; Cauz, D.; Cavaliere, V.; Cavalli-Sforza, M.; Cerri, A.; Cerrito, L.; Chen, Y. C.; Chertok, M.; Chiarelli, G.; Chlachidze, G.; Chlebana, F.; Cho, K.; Chokheli, D.; Chung, W. H.; Chung, Y. S.; Ciobanu, C. I.; Ciocci, M. A.; Clark, A.; Clarke, C.; Compostella, G.; Convery, M. E.; Conway, J.; Corbo, M.; Cordelli, M.; Cox, C. A.; Cox, D. J.; Crescioli, F.; Cuevas, J.; Culbertson, R.; Dagenhart, D.; d’Ascenzo, N.; Datta, M.; de Barbaro, P.; Dell’Orso, M.; Demortier, L.; Deninno, M.; Devoto, F.; d’Errico, M.; Di Canto, A.; Di Ruzza, B.; Dittmann, J. R.; D’Onofrio, M.; Donati, S.; Dong, P.; Dorigo, M.; Dorigo, T.; Ebina, K.; Elagin, A.; Eppig, A.; Erbacher, R.; Errede, S.; Ershaidat, N.; Eusebi, R.; Farrington, S.; Feindt, M.; Fernandez, J. P.; Field, R.; Flanagan, G.; Forrest, R.; Frank, M. J.; Franklin, M.; Freeman, J. C.; Funakoshi, Y.; Furic, I.; Gallinaro, M.; Garcia, J. E.; Garfinkel, A. F.; Garosi, P.; Gerberich, H.; Gerchtein, E.; Giagu, S.; Giakoumopoulou, V.; Giannetti, P.; Gibson, K.; Ginsburg, C. M.; Giokaris, N.; Giromini, P.; Giurgiu, G.; Glagolev, V.; Glenzinski, D.; Gold, M.; Goldin, D.; Goldschmidt, N.; Golossanov, A.; Gomez, G.; Gomez-Ceballos, G.; Goncharov, M.; González, O.; Gorelov, I.; Goshaw, A. T.; Goulianos, K.; Grinstein, S.; Grosso-Pilcher, C.; Group, R. C.; Guimaraes da Costa, J.; Hahn, S. R.; Halkiadakis, E.; Hamaguchi, A.; Han, J. Y.; Happacher, F.; Hara, K.; Hare, D.; Hare, M.; Harr, R. F.; Hatakeyama, K.; Hays, C.; Heck, M.; Heinrich, J.; Herndon, M.; Hewamanage, S.; Hocker, A.; Hopkins, W.; Horn, D.; Hou, S.; Hughes, R. E.; Hurwitz, M.; Husemann, U.; Hussain, N.; Hussein, M.; Huston, J.; Introzzi, G.; Iori, M.; Ivanov, A.; James, E.; Jang, D.; Jayatilaka, B.; Jeon, E. J.; Jindariani, S.; Jones, M.; Joo, K. K.; Jun, S. Y.; Junk, T. R.; Kamon, T.; Karchin, P. E.; Kasmi, A.; Kato, Y.; Ketchum, W.; Keung, J.; Khotilovich, V.; Kilminster, B.; Kim, D. H.; Kim, H. S.; Kim, J. E.; Kim, M. J.; Kim, S. B.; Kim, S. H.; Kim, Y. K.; Kim, Y. J.; Kimura, N.; Kirby, M.; Klimenko, S.; Knoepfel, K.; Kondo, K.; Kong, D. J.; Konigsberg, J.; Kotwal, A. V.; Kreps, M.; Kroll, J.; Krop, D.; Kruse, M.; Krutelyov, V.; Kuhr, T.; Kurata, M.; Kwang, S.; Laasanen, A. T.; Lami, S.; Lammel, S.; Lancaster, M.; Lander, R. L.; Lannon, K.; Lath, A.; Latino, G.; LeCompte, T.; Lee, E.; Lee, H. S.; Lee, J. S.; Lee, S. W.; Leo, S.; Leone, S.; Lewis, J. D.; Limosani, A.; Lin, C.-J.; Lindgren, M.; Lipeles, E.; Lister, A.; Litvintsev, D. O.; Liu, C.; Liu, H.; Liu, Q.; Liu, T.; Lockwitz, S.; Loginov, A.; Lucchesi, D.; Lueck, J.; Lujan, P.; Lukens, P.; Lungu, G.; Lys, J.; Lysak, R.; Madrak, R.; Maeshima, K.; Maestro, P.; Malik, S.; Manca, G.; Manousakis-Katsikakis, A.; Margaroli, F.; Marino, C.; Martínez, M.; Mastrandrea, P.; Matera, K.; Mattson, M. E.; Mazzacane, A.; Mazzanti, P.; McFarland, K. S.; McIntyre, P.; McNulty, R.; Mehta, A.; Mehtala, P.; Mesropian, C.; Miao, T.; Mietlicki, D.; Mitra, A.; Miyake, H.; Moed, S.; Moggi, N.; Mondragon, M. N.; Moon, C. S.; Moore, R.; Morello, M. J.; Morlock, J.; Movilla Fernandez, P.; Mukherjee, A.; Muller, Th.; Murat, P.; Mussini, M.; Nachtman, J.; Nagai, Y.; Naganoma, J.; Nakano, I.; Napier, A.; Nett, J.; Neu, C.; Neubauer, M. S.; Nielsen, J.; Nodulman, L.; Noh, S. Y.; Norniella, O.; Oakes, L.; Oh, S. H.; Oh, Y. D.; Oksuzian, I.; Okusawa, T.; Orava, R.; Ortolan, L.; Pagan Griso, S.; Pagliarone, C.; Palencia, E.; Papadimitriou, V.; Paramonov, A. A.; Patrick, J.; Pauletta, G.; Paulini, M.; Paus, C.; Pellett, D. E.; Penzo, A.; Phillips, T. J.; Piacentino, G.; Pianori, E.; Pilot, J.; Pitts, K.; Plager, C.; Pondrom, L.; Poprocki, S.; Potamianos, K.; Prokoshin, F.; Pranko, A.; Ptohos, F.; Punzi, G.; Rahaman, A.; Ramakrishnan, V.; Ranjan, N.; Redondo, I.; Renton, P.; Rescigno, M.; Riddick, T.; Rimondi, F.; Ristori, L.; Robson, A.; Rodrigo, T.; Rodriguez, T.; Rogers, E.; Rolli, S.; Roser, R.; Ruffini, F.; Ruiz, A.; Russ, J.; Rusu, V.; Safonov, A.; Sakumoto, W. K.; Sakurai, Y.; Santi, L.; Sato, K.; Saveliev, V.; Savoy-Navarro, A.; Schlabach, P.; Schmidt, A.; Schmidt, E. E.; Schwarz, T.; Scodellaro, L.; Scribano, A.; Scuri, F.; Seidel, S.; Seiya, Y.; Semenov, A.; Sforza, F.; Shalhout, S. Z.; Shears, T.; Shepard, P. F.; Shimojima, M.; Shochet, M.; Shreyber-Tecker, I.; Simonenko, A.; Sinervo, P.; Sliwa, K.; Smith, J. R.; Snider, F. D.; Soha, A.; Sorin, V.; Song, H.; Squillacioti, P.; Stancari, M.; St. Denis, R.; Stelzer, B.; Stelzer-Chilton, O.; Stentz, D.; Strologas, J.; Strycker, G. L.; Sudo, Y.; Sukhanov, A.; Suslov, I.; Takemasa, K.; Takeuchi, Y.; Tang, J.; Tecchio, M.; Teng, P. K.; Thom, J.; Thome, J.; Thompson, G. A.; Thomson, E.; Toback, D.; Tokar, S.; Tollefson, K.; Tomura, T.; Tonelli, D.; Torre, S.; Torretta, D.; Totaro, P.; Trovato, M.; Ukegawa, F.; Uozumi, S.; Varganov, A.; Vázquez, F.; Velev, G.; Vellidis, C.; Vidal, M.; Vila, I.; Vilar, R.; Vizán, J.; Vogel, M.; Volpi, G.; Wagner, P.; Wagner, R. L.; Wakisaka, T.; Wallny, R.; Wang, S. M.; Warburton, A.; Waters, D.; Wester, W. C.; Whiteson, D.; Wicklund, A. B.; Wicklund, E.; Wilbur, S.; Wick, F.; Williams, H. H.; Wilson, J. S.; Wilson, P.; Winer, B. L.; Wittich, P.; Wolbers, S.; Wolfe, H.; Wright, T.; Wu, X.; Wu, Z.; Yamamoto, K.; Yamato, D.; Yang, T.; Yang, U. K.; Yang, Y. C.; Yao, W.-M.; Yeh, G. P.; Yi, K.; Yoh, J.; Yorita, K.; Yoshida, T.; Yu, G. B.; Yu, I.; Yu, S. S.; Yun, J. C.; Zanetti, A.; Zeng, Y.; Zhou, C.; Zucchelli, S.

    2012-04-02

    This paper presents a search for standard model Higgs boson production in association with a W boson using events recorded by the CDF experiment in a data set corresponding to an integrated luminosity of 5.6 fb⁻¹. The search is performed using a matrix element technique in which the signal and background hypotheses are used to create a powerful discriminator. The discriminant output distributions for signal and background are fit to the observed events using a binned likelihood approach to search for the Higgs boson signal. We find no evidence for a Higgs boson, and 95% confidence level (C.L.) upper limits are set on σ(pp̄→WH)×B(H→bb¯). The observed limits range from 3.5 to 37.6 relative to the standard model expectation for Higgs boson masses between mH=100 GeV/c² and mH=150 GeV/c². The 95% C.L. expected limit is estimated from the median of an ensemble of simulated experiments and varies between 2.9 and 32.7 relative to the production rate predicted by the standard model over the Higgs boson mass range studied.

  19. High-contrast process using a positive-tone resist with antistatic coating and high-energy (100-keV) e-beam lithography for fabricating diffractive optical elements (DOE) on quartz

    NASA Astrophysics Data System (ADS)

    Poli, Louis C.; Kondek, Christine A.; Shoop, Barry L.; McLane, George F.

    1995-06-01

    Diffractive optical elements (DOE) are becoming important as optical signal processing elements in increasingly diverse applications. These elements, fabricated on quartz, may be used as phase shift type masks or as embedded components that implement a transfer function within a processing network. A process is under development for the fabrication of a DOE implementing a Jervis error diffusion kernel for research in half tone image processing. Dry etching is performed after lithography and pattern transfer through a nickel mask. This results in etched areal features on the substrate. An optical diffraction medium is thus created. Lithographic patterning is done by e-beam lithography (EBL) to realize small features, but also offers the important advantage of a large depth of field which relaxes the problem of complex surface topology. The recent availability of high energy (100 KeV) lithography tools provides a capability for precision overlay, small feature resolution, and enhanced image contrast through a lower induced proximity effect. Patterning by EBL on insulating substrates is complicated by the necessity of providing a vehicle for the avoidance of charge buildup on the surface. In a previously presented paper a methodology was shown for the use of TQV-501 (Nitto Chemical) antistatic compound as a final spin on film for use with PMMA and SAL-601 (Shipley). In this current work, a process is described using EBL and a high performance positive resist working with a final film layer of antistatic TQV-501 on a nickel coated wafer. The process may then be reapplied to realize additional lithographic levels in registration, for multilevel DOE components. High energy (100 KeV) EBL is used to provide high quality pattern definition. The e-beam sensitive resist, ZEP-320-37 (Nagase Chemical) in dilution, together with a top film layer of TQV-501 serves as a bilevel resist system and is used for patterning the desired image before definition of the nickel mask through

  20. Cortical Dynamics of Figure-Ground Separation in Response to 2D Pictures and 3D Scenes: How V2 Combines Border Ownership, Stereoscopic Cues, and Gestalt Grouping Rules

    PubMed Central

    Grossberg, Stephen

    2016-01-01

    The FACADE model, and its laminar cortical realization and extension in the 3D LAMINART model, have explained, simulated, and predicted many perceptual and neurobiological data about how the visual cortex carries out 3D vision and figure-ground perception, and how these cortical mechanisms enable 2D pictures to generate 3D percepts of occluding and occluded objects. In particular, these models have proposed how border ownership occurs, but have not yet explicitly explained the correlation between multiple properties of border ownership neurons in cortical area V2 that were reported in a remarkable series of neurophysiological experiments by von der Heydt and his colleagues; namely, border ownership, contrast preference, binocular stereoscopic information, selectivity for side-of-figure, Gestalt rules, and strength of attentional modulation, as well as the time course during which such properties arise. This article shows how, by combining 3D LAMINART properties that were discovered in two parallel streams of research, a unified explanation of these properties emerges. This explanation proposes, moreover, how these properties contribute to the generation of consciously seen 3D surfaces. The first research stream models how processes like 3D boundary grouping and surface filling-in interact in multiple stages within and between the V1 interblob—V2 interstripe—V4 cortical stream and the V1 blob—V2 thin stripe—V4 cortical stream, respectively. Of particular importance for understanding figure-ground separation is how these cortical interactions convert computationally complementary boundary and surface mechanisms into a consistent conscious percept, including the critical use of surface contour feedback signals from surface representations in V2 thin stripes to boundary representations in V2 interstripes. Remarkably, key figure-ground properties emerge from these feedback interactions. The second research stream shows how cells that compute absolute disparity

  1. Cortical Dynamics of Figure-Ground Separation in Response to 2D Pictures and 3D Scenes: How V2 Combines Border Ownership, Stereoscopic Cues, and Gestalt Grouping Rules.

    PubMed

    Grossberg, Stephen

    2015-01-01

    The FACADE model, and its laminar cortical realization and extension in the 3D LAMINART model, have explained, simulated, and predicted many perceptual and neurobiological data about how the visual cortex carries out 3D vision and figure-ground perception, and how these cortical mechanisms enable 2D pictures to generate 3D percepts of occluding and occluded objects. In particular, these models have proposed how border ownership occurs, but have not yet explicitly explained the correlation between multiple properties of border ownership neurons in cortical area V2 that were reported in a remarkable series of neurophysiological experiments by von der Heydt and his colleagues; namely, border ownership, contrast preference, binocular stereoscopic information, selectivity for side-of-figure, Gestalt rules, and strength of attentional modulation, as well as the time course during which such properties arise. This article shows how, by combining 3D LAMINART properties that were discovered in two parallel streams of research, a unified explanation of these properties emerges. This explanation proposes, moreover, how these properties contribute to the generation of consciously seen 3D surfaces. The first research stream models how processes like 3D boundary grouping and surface filling-in interact in multiple stages within and between the V1 interblob-V2 interstripe-V4 cortical stream and the V1 blob-V2 thin stripe-V4 cortical stream, respectively. Of particular importance for understanding figure-ground separation is how these cortical interactions convert computationally complementary boundary and surface mechanisms into a consistent conscious percept, including the critical use of surface contour feedback signals from surface representations in V2 thin stripes to boundary representations in V2 interstripes. Remarkably, key figure-ground properties emerge from these feedback interactions. The second research stream shows how cells that compute absolute disparity in

  2. Elemental ZOO

    NASA Astrophysics Data System (ADS)

    Helser, Terry L.

    2003-04-01

    This puzzle uses the symbols of 39 elements to spell the names of 25 animals found in zoos. Underlined spaces and the names of the elements serve as clues. To solve the puzzle, students must find the symbols that correspond to the elemental names and rearrange them into the animals' names.