WorldWideScience

Sample records for hg mn mo

  1. Concentrations of As, Ca, Cd, Co, Cr, Cu, Fe, Hg, K, Mg, Mn, Mo, Na, Ni, Pb, and Zn in uruguayan rice determined by atomic absorption spectrometry

    Directory of Open Access Journals (Sweden)

    Mario E. Rivero Huguet

    2011-04-01

    Full Text Available The United Nations General Assembly declared the year 2004 the International Year of Rice and the concept "Rice is life". The largest nutritional problems occurring globally are protein-energy malnutrition, and Ca, Fe, I, Zn, and vitamin A deficiency. In this report, 49 rice samples (Oryza sativa L. were digested by dry ashing in order to determine As, Cd, Cr, and Pb by ETA-AAS; while Ca, Co, Cu, Fe, K, Mg, Mo, Mn, Na, Ni, and Zn were determined by FAAS; and Hg by CV-AAS using microwave-assisted decomposition. The following concentration ranges were obtained for Ca (9.1-15 mg/100 g, Cd (2.30-4.12 µg/kg, Co (41-60 µg/kg, Cu (1.33-180 mg/kg, Fe (4.41-7.15 mg/kg, K (167-217 mg/100 g, Mg (45-121 mg/100 g, Mo (0.52-0.97 mg/kg, Mn (5.45-25.4 mg/kg, Na (0.95-2.50 mg/100g, Ni (0.53-0.72 mg/kg, and Zn (5.86-12.6 mg/kg. Mean recoveries of elements from fortified rice were: 87±12% for As, 95.3±8.9% for Ca, 106.2±7.7% for Cd, 103.3±6.5% for Co, 89.4±8.1% for Cr, 99.3±4.6% for Cu, 103±10% for Fe, 96.3±9.3% for Hg, 95.4±12% for K, 98.3±8.0% for Mg, 93.4±7.8% for Mo, 95.3±9.9% for Mn, 89±12% for Na, 90.3±9.7% for Ni, 91.2±5.5% for Pb and 92.0±9.4% for Zn. The concentrations of the minerals and microelements studied fall within the typical range of rice grown around the world. Potassium was the most abundant mineral, followed by Mg and Ca; among microelements, the concentrations of Cu, Fe, Mo, Mn, Na, and Zn in rice were outstanding. It was also found that the milling process highly affects the K, Mg, Mn, Na, and Zn concentrations, while it has little influence on Ca, Co, Cu, and Fe. On the other hand, there is a loss of Ca, Fe, and Mn during the parboiling process. Recent studies have shown the potential to exploit the genetic variation of rice seeds with regard to the concentration of some minerals (Ca, Fe, Zn, etc. without affecting yield or adding new traits. All rice samples tested showed lower levels of As, Cd, Hg, and Pb in comparison

  2. Magnetic fields of HgMn stars

    CERN Document Server

    Hubrig, S; Ilyin, I; Korhonen, H; Schoeller, M; Savanov, I; Arlt, R; Castelli, F; Curto, G Lo; Briquet, M; Dall, T H

    2012-01-01

    The frequent presence of weak magnetic fields on the surface of spotted late-B stars with HgMn peculiarity in binary systems has been controversial during the two last decades. We re-analyse available spectropolarimetric material by applying the moment technique on spectral lines of inhomogeneously distributed elements separately. Furthermore, we present new determinations of the mean longitudinal magnetic field for the HgMn star HD65949 and the hotter analog of HgMn stars, the PGa star HD19400, using FORS2 installed at the VLT. We also give new measurements of the eclipsing system AR Aur with a primary star of HgMn peculiarity which were obtained with the SOFIN spectropolarimeter installed at the Nordic Optical Telescope. We downloaded from the ESO archive the publically available HARPS spectra for eight HgMn stars and one normal and one superficially normal B-type star obtained in 2010. The application of the moment technique to the HARPS and SOFIN spectra allowed us to study the presence of the longitudina...

  3. Magnetic fields of HgMn stars

    DEFF Research Database (Denmark)

    Hubrig, S.; Gonzalez, J. F.; Ilyin, I.

    2012-01-01

    Context. The frequent presence of weak magnetic fields on the surface of spotted late-B stars with HgMn peculiarity in binary systems has been controversial during the two last decades. Recent studies of magnetic fields in these stars using the least-squares deconvolution (LSD) technique have fai...

  4. Of Variability, or its Absence, in HgMn Stars

    CERN Document Server

    Turcotte, S

    2003-01-01

    Current models and observations of variability in HgMn stars disagree. We present here the models that argue for pulsating HgMn stars with properties similar to those of Slowly Pulsating B Stars. The lack of observed variable HgMn stars suggests that some physical process is missing from the models. Some possibilities are discussed.

  5. Magnetic fields of HgMn stars

    DEFF Research Database (Denmark)

    Hubrig, S.; González, J. F.; Ilyin, I.

    2012-01-01

    Context. The frequent presence of weak magnetic fields on the surface of spotted late-B stars with HgMn peculiarity in binary systems has been controversial during the two last decades. Recent studies of magnetic fields in these stars using the least-squares deconvolution (LSD) technique have...... failed to detect magnetic fields, indicating an upper limit on the longitudinal field between 8 and 15G. In these LSD studies, assumptions were made that all spectral lines are identical in shape and can be described by a scaled mean profile. Aims. We re-analyse the available spectropolarimetric material...

  6. The Chevrel phase HgMo6S8

    Directory of Open Access Journals (Sweden)

    Michel Potel

    2009-05-01

    Full Text Available The crystal structure of HgMo6S8, mercury(II hexamolybdenum octasulfide, is based on (Mo6S8S6 cluster units (overline{3} symmetry interconnected through interunit Mo—S bonds. The Hg2+ cations occupy large voids between the different cluster units and are covalently bonded to two S atoms. The Hg atoms and one S atom lie on sites with crystallographic overline{3} and 3 symmetry, respectively. Refinement of the occupancy factor of the Hg atom led to the composition Hg0.973 (3Mo6S8.

  7. Horizontal Branch stars as AmFm/HgMn stars

    CERN Document Server

    Michaud, G

    2008-01-01

    Recent observations and models for horizontal branch stars are briefly described and compared to models for AmFm stars. The limitations of those models are emphasized by a comparison to observations and models for HgMn stars.

  8. Searching for Line Profile Variability in HgMn Stars

    CERN Document Server

    Turcotte, S; Knoglinger, P

    2002-01-01

    Spectra of four non-magnetic chemically peculiar late B type stars (HgMn) stars are analysed to detect periodic spectral line variations (LPVs). A procedure developed to study LPVs in Slowly Pulsating B stars has been adopted as pulsational properties of HgMn stars should be expected to be similar. In the preliminary results discussed here no conclusive evidence for periodic LPVs was uncovered. A more sensitive re-analysis of the data is under way.

  9. Spectroscopic variability and magnetic fields of HgMn stars

    CERN Document Server

    Hubrig, S; Ilyin, I; Korhonen, H; Savanov, I S; Dall, T; Schoeller, M; Cowley, C R; Briquet, M; Arlt, R

    2011-01-01

    The discovery of exotic abundances, chemical inhomogeneities, and weak magnetic fields on the surface of late B-type primaries in spectroscopic binaries has important implications not only for our understanding of the formation mechanisms of stars with Hg and Mn peculiarities themselves, but also for the general understanding of B-type star formation in binary systems. The origin of the abundance anomalies observed in late B-type stars with HgMn peculiarity is still poorly understood. The connection between HgMn peculiarity and membership in binary and multiple systems is supported by our observations during the last decade. The important result achieved in our studies of a large sample of HgMn stars is the finding that most HgMn stars exhibit spectral variability of various chemical elements, proving that the presence of an inhomogeneous distribution on the surface of these stars is a rather common characteristic and not a rare phenomenon. Further, in the studied systems, we found that all components are che...

  10. Are there tangled magnetic fields on HgMn stars?

    CERN Document Server

    Kochukhov, O; Piskunov, N; Jeffers, S V; Johns-Krull, C M; Keller, C U; Rodenhuis, M; Snik, F; Stempels, H C; Valenti, J A

    2013-01-01

    Several recent spectrophotometric studies failed to detect significant global magnetic fields in late-B HgMn chemically peculiar stars, but some investigations have suggested the presence of strong unstructured or tangled fields in these objects. We used detailed spectrum synthesis analysis to search for evidence of tangled magnetic fields in high-quality observed spectra of 8 slowly rotating HgMn stars and one normal late-B star. We also evaluated recent sporadic detections of weak longitudinal magnetic fields in HgMn stars based on the moment technique. Our analysis of the Zeeman broadening of magnetically sensitive spectral lines reveals no evidence of tangled magnetic fields in any of the studied HgMn or normal stars. We infer upper limits of 200-700 G for the mean magnetic field modulus -- much smaller than the field strengths implied by studies based on differential magnetic line intensification and quadratic field diagnostics. The new HARPSpol longitudinal field measurements for the extreme HgMn star H...

  11. Magnetic phase diagrams of α-MnMoO 4

    Science.gov (United States)

    Ehrenberg, H.; Schwarz, B.; Weitzel, H.

    2006-10-01

    Field-induced spin-flop transitions in α-MnMoO 4 are summarized in magnetic H-T phase diagrams for different directions of the applied magnetic field up to 12 T. The antiferromagnetic arrangement in the spin-flop phase is preserved at least up to this field for a field parallel to the easy direction. This high transition field is in contrast to the low one of α-NiMoO 4 and favours a model, based on dominant antiferromagnetic supersuperexchange couplings in α-MnMoO 4 over a ferromagnetic Mn 4 "cluster" model. The Néel temperature of 9.8(1) K was determined from the corresponding specific-heat anomaly, measured on a single crystal of α-MnMoO 4.

  12. Effects of salinity and humic acid on the sorption of Hg on Fe and Mn hydroxides.

    Science.gov (United States)

    Liang, Peng; Li, Yi-Chun; Zhang, Chan; Wu, Sheng-Chun; Cui, Hao-Jie; Yu, Shen; Wong, Ming H

    2013-01-15

    The objective of this study was to investigate the influence of humic acid (HA) and salinity on adsorption of Hg on the amorphous and crystalline of iron and manganese hydroxides. The results show that the adsorption of Hg(2+) on Fe and Mn hydroxides was inhibited in marine system due to the formation of stable, nonsorbing aqueous HgCl(2) complexes in solution. Moreover, Cl(-) inhibited the Hg(2+) adsorption more severely on amorphous than crystalline hydroxides. The addition of HA inhibited Hg(2+) adsorption on Fe and Mn hydroxides in freshwater system might be attributed to the competition between Hg(2+) and HA on adsorption to Fe and Mn hydroxides. In contrast, the addition of HA promoted Hg(2+) adsorption on Fe and Mn hydroxides in the marine system, which might be due to the addition of humic acid resulted in the reaction between Cl(-) and HA, and therefore the reducing of Cl(-) promoted more Hg(2+) on Fe and Mn hydroxides. In addition, the influence of HA on Hg(2+) adsorption on Fe and Mn hydroxides are more visible for crystalline than amorphous hydroxides.

  13. Abundancias químicas de dos binarias de HgMn

    Science.gov (United States)

    Gonzalez, E. J.; González, J. F.; Collado, A. E.

    We present the results of the abundance analysis of two HgMn single-line binary systems: NGC 2287-106 and NGC 6025-14. The spectroscopic ob- servations have been carried out at the Complejo Astronómico el Leon-cito (CASLEO) with the REOSC spectrograph in cross-dispersion mode, cov- ering the spectral range 3800-5800 ≈. Compared to the Sun, NGC 6025-14 shows great overabundances of Hg, Mn, P, Ga and Xe, while Hg, Mn, Sr, Pt and Zr are overabundant in NGC 2287-106. FULL TEXT IN SPANISH

  14. Lattice dynamical properties of MnTe, HgTe and their mixed semiconductor MnHg1−Te

    Indian Academy of Sciences (India)

    A K Kushwaha

    2015-12-01

    In the present paper, the phonon dispersion relations, phonon density of states and Debye characteristics of mixed semiconductor MnHg1−Te and the end members MnTe and HgTe using three-body shell model were studied. The model involves 11 disposable parameters and incorporates the effect of the short-range repulsive interactions up to and including the second nearest neighbours, in addition to the long-range Coulombic interactions in the framework of the rigid-shell model with both the ions polarizable. The comparisons of the theoretical results with the available experimental results were in good agreement.

  15. Magnetism, chemical spots, and stratification in the HgMn star phi Phoenicis

    CERN Document Server

    Makaganiuk, V; Piskunov, N; Jeffers, S V; Johns-Krull, C M; Keller, C U; Rodenhuis, M; Snik, F; Stempels, H C; Valenti, J A

    2011-01-01

    Mercury-manganese (HgMn) stars have been considered as non-magnetic and non-variable chemically peculiar (CP) stars for a long time. However, recent discoveries of the variability in spectral line profiles suggested an inhomogeneous surface distribution of chemical elements in some HgMn stars. From the studies of other CP stars it is known that magnetic field plays a key role in the formation of surface spots. All attempts to find magnetic fields in HgMn stars yielded negative results. In this study, we investigate a possible presence of the magnetic field in phi Phe (HD 11753) and reconstruct surface distribution of chemical elements that show variability in spectral lines. We also test a hypothesis that magnetic field is concentrated in chemical spots and look into the possibility that some chemical elements are stratified with depth in the stellar atmosphere.

  16. Obtainment of Hg-free Mn/Zn solutions from spent alkaline batteries; Obtencion de soluciones de Mn/Zn libres de Hg provenientes de pilas alcalinas gastadas

    Energy Technology Data Exchange (ETDEWEB)

    Perez-Nicolas, L.; Espinosa-Ramirez, I. [Instituto Politecnico Nacional, UPALM, Mexico, D.F. (Mexico)]. E-mail: lepeni@hotmail.com; Aguilar, M. [Instituto de Fisica, UNAM, Mexico, D.F. (Mexico); Palacios-Beas, E. [Instituto Politecnico Nacional, UPALM, Mexico, D.F. (Mexico)

    2009-09-15

    As in many other countries, the excessive consumption of alkaline batteries in Mexico has generated highly contaminating wastes, with heavy metal contents such as Mn, Zn, Fe, Hg, Cu and Ni, among others. This has caused a large degree of environmental degradation with repercussions for the health of living beings. Because there are no regulations regarding the disposal of spent batteries, they are thrown out with the rest of the domestic wastes or directly into nature, ending up in open-air landfills or containers where they are incinerated, thereby contaminating the planet's environment, soil and springs. The present work studies the obtainment of solutions of Hg-free Mn and Zn (Mn/Zn {>=} 1) from spent alkaline batteries for use in synthesis of (Mn,Zn)Fe{sub 2}O{sub 4} ferrite by a wet method. The effect is analyzed of the dissolution medium (H{sub 2}SO{sub 4}/H{sub 2}O{sub 2}, HCl and HCl/NO{sub 3}) temperature and time on the percentage of dissolution of the metals present in the electrode material, characterized by atomic absorption (AA) spectroscopy and x-ray diffraction (XRD). The results of the investigation indicate that the best dissolution conditions are MD=H{sub 2}SO{sub 4}/H{sub 2}O{sub 2}, T=50 degrees Celsius and t =30 min, where 94.1 and 90.7 % (w/w) of Mn and Zn are obtained, respectively, with Mn/Zn = 1.51. The mercury content was determined to be 3.91%, higher than that stated by the battery specifications, which is recovered by dissolving with HCl/HNO{sub 3} in the residual solid. [Spanish] En Mexico como en muchos otros paises, el consumo excesivo de pilas alcalinas ha generado desechos altamente contaminantes, con contenidos de metales pesados como Mn, Zn, Fe, Hg, Cu y Ni entre otros, que han provocado un gran deterioro en el medio ambiente repercutiendo en la salud de los seres vivos. Dado que no se tiene una regulacion en cuanto a la disposicion de pilas gastadas, estas se desechan con el resto de las residuos domesticos o directamente

  17. Synthesis and Crystal Structure of New Coordination Compound Mn2Hg4(SCN)12%新型配合物Mn2Hg4(SCN)12的合成与晶体结构分析

    Institute of Scientific and Technical Information of China (English)

    李广慧; 方奇; 薛刚; 于文涛

    2005-01-01

    A new inorganic coordination compound Mn2Hg4(SCN)12 was synthesized. The grown crystals were characterized by elemental analysis, infrared spectroscopic analysis and powder crystal X-ray diffraction in detail. The crystal structure of Mn2Hg4(SCN)12 was determined by single-crystal X-ray diffraction. It belongs to monoclinic system, P21/c space group. The cell dimensions are: a=1.171 6 nm, b=1.431 05 nm, c=2.105 1 nm,β=100.738°,and Z=4. In the structure of it, half of Mn2+ cations have five-coordinate number, and other half of Mn2+ cations have six-coordinate number; 3/4 of Hg2+ cations are coordinated by four SCN-, 1/4 of Hg2+ cations are coordinated by three SCN- and one NCS-, all the coordination geometry of Hg2+ show slightly distorted tetrahedrons. CCDC:244939.

  18. Directional Solidification and Characterization of Hg(0.89) Mn(0.11)Te

    Science.gov (United States)

    Price, M. W.; Scripa, R. N.; Lehoczky. S. L.; Szofran, F. R.; Su, C.-H.

    1998-01-01

    Two boules of Hg(0.89)Mn(0.11)Te(MMT) were solidified using the vertical Bridgman-Stockbarger method. Translation rates of 0.09 and 0. 18 microns/s were used. The influence of growth rate on axial compositional homogeneity in the MMT boules was evaluated experimentally by conducting precision density measurements on radial slices taken from each boule. In addition, Plane Front Solidification theory and segregation coefficient (k) data for the Hg(1-x)Mn(x)Te system were used to fit theoretical composition profiles to the measured MMT axial composition profiles. The strong correlation between the measured and calculated MMT axial composition profiles indicates diffusion dominated axial solute redistribution in the boules under the applied growth conditions. The analysis of the MMT axial composition profiles by Plane Front Solidification theory allowed the calculation of the effective diffusion coefficient (D(eff) = 3.5 x l0(exp -5) sq cm/s). The k-values for the Hg(1-x)Mn(x)Te system and the D(sub eff) - value were then used to verify that both boules were solidified under conditions which did not exceed the Constitutional Supercooling Criteria under ideal conditions. Finally, a preliminary examination of the radial compositional variation in each MMT was made using Fourier Transform Infra-Red Spectroscopy (FTIR). The radial homogeneity in the MMT boules was found to be comparable for both translation rates.

  19. Magnetic Properties of Diluted Magnetic Semiconductor Hg0.89Mn0.11Te

    Institute of Scientific and Technical Information of China (English)

    WANG Zewen; JIE Wanqi

    2015-01-01

    The magnetization of Hg0.89Mn0.11Te single crystal grown by vertical Bridgman method was studied by using superconducting quantum interference device magnetometer (SQUID Magnetometer). First, magnetization measurements were done under various magnetic ifeld strengths from-20 kOe to 20 kOe at 5 K, 15 K, and 77 K, respectively. Then, the magnetizations were measured with continuous changes of temperature in the range from 5 K to 300 K under the magnetic ifeld of 0.1 kOe and 10 kOe, respectively. The modiifed Brillouin function was well fitted with the data of magnetization vs. magnetic field strength. The analysis indicated that there was an antiferromagnetic exchange coupling among Mn2+ions. The results of reciprocal susceptibility vs. temperature ift Curie-Weiss law very well at the temperatures above 40 K, but deviate from the law from 5 K to 40 K, which shows that the antiferromagnetic exchange coupling among Mn2+ions increases in the lower temperature range below 40 K. The experimental result was explained by extending higher-order terms in the calculation of susceptibility and fitted by a power law function. The measurements reveal that Hg0.89Mn0.11Te possesses paramagnetic properties at temperatures from 5 K to 300 K.

  20. First Principles Study on Electronic Structures of Mn2+:CdMoO4 Crystals

    Institute of Scientific and Technical Information of China (English)

    WANG Xi-En; LIU Ting-Yu; ZHANG Qi-Ren; ZHANG Hai-Yan; SONG Min; GUO Xiao-Feng; YIN Ji-Gang

    2008-01-01

    @@ Electronic structures of the Mn2+:CdMoO4 crystal are studied within the framework of the fully relativistic self-consistent Dirac-Slater theory,using a numerically discrete variation (DV-Xα)method.The calculated results indicate that the 3d states of Mn have donor energy level in the forbidden band of CdMoO4 crystal.The transition energy of O 2p→Mn 3d is 3.12 eV under excitation corresponding electronic transition being O2-+Mn2+ hvex=3.12 eV→ O-+Mn+hvem→O2+Mn2+.

  1. Hydrothermal synthesis of micrometer sized HgMoO{sub 4} flowers formed by nanorods

    Energy Technology Data Exchange (ETDEWEB)

    Jia Runping, E-mail: jiarp@sit.edu.cn; Zhang Yingqiang, E-mail: sh_yqzhang@sina.co [Shanghai Institute of Technology, School of Materials Science and Engineering (China)

    2010-10-15

    Micrometer sized HgMoO{sub 4} flowers formed by nanorods were prepared by a selected hydrothermal method using a mixture of ethanol and water as a reaction medium, which were characterized by scanning electron microscopy, X-ray diffractometer (XRD), FT-IR spectrometry, photoluminescence spectrometry, and UV-visible spectrometry. Results indicated that the micrometer sized flowers consisted of mercury molybdate nanorods, and the monoclinic wolframite-type structure of the flowers was confirmed by both XRD and FT-IR spectrometry. A blue shift of the photoluminescence peaks and a broadening of XRD peaks were observed, which increased with ethanol fraction in the reaction medium.

  2. Synthesis, phase and reaction mechanism of nonlinear optical material MnTeMoO{sub 6}

    Energy Technology Data Exchange (ETDEWEB)

    Jin, Chengguo; Shao, Juxiang; Yang, Junsheng; Wan, Mingjie [Yibin University, Key Laboratory of Computational Physics of Sichuan Province, Yibin (China); Yibin University, School of Physics and Electronic Engineering, Yibin (China); Luo, Huafeng [Yibin University, College of Chemistry and Chemical Engineering, Yibin (China); Huang, Xingyong [Yibin University, School of Physics and Electronic Engineering, Yibin (China); Wang, Fanhou [Yibin University, Key Laboratory of Computational Physics of Sichuan Province, Yibin (China)

    2016-09-15

    Pure polycrystalline MnTeMoO{sub 6} is highly desirable to crystal growth. Polycrystalline MnTeMoO{sub 6} has been synthesized by solid-state reaction techniques. The optimized preparation process, phase purity and reaction mechanism of polycrystalline MnTeMoO{sub 6} were investigated. The reaction will be paused if the atoms cannot pass through the grain boundary and restarted after ground intimately. A new method combined with X-ray diffraction and microscopic observation is employed to determine the phase purity of polycrystalline MnTeMoO{sub 6}. Pure polycrystalline MnTeMoO{sub 6} with gray color and single crystalline phase can be obtained after the reactant was calcined at 500 C for 20 h three times and can be used to crystal growth. This method for determining the phase purity of powder sample can be used in the synthesis of other polycrystalline powders. (orig.)

  3. No magnetic field in the spotted HgMn star mu Leporis

    CERN Document Server

    Kochukhov, O; Piskunov, N; Jeffers, S V; Johns-Krull, C M; Keller, C U; Rodenhuis, M; Snik, F; Stempels, H C; Valenti, J A

    2011-01-01

    Chemically peculiar stars of the mercury-manganese (HgMn) type represent a new class of spotted late-B stars, in which evolving surface chemical inhomogeneities are apparently unrelated to the presence of strong magnetic fields but are produced by some hitherto unknown astrophysical mechanism. The goal of this study is to perform a detailed line profile variability analysis and carry out a sensitive magnetic field search for one of the brightest HgMn stars - mu Lep. We acquired a set of very high-quality intensity and polarization spectra of mu Lep with the HARPSpol polarimeter. These data were analyzed with the multiline technique of least-squares deconvolution in order to extract information on the magnetic field and line profile variability. Our spectra show very weak but definite variability in the lines of Sc, all Fe-peak elements represented in the spectrum of mu Lep, as well as Y, Sr, and Hg. Variability might also be present in the lines of Si and Mg. Anomalous profile shapes of Ti II and Y II lines s...

  4. On the concentration and separation of the trace-elements fe, cu, zn, mn, pb, mo and co : Paper chromatography

    NARCIS (Netherlands)

    Erkelens, P.C. van

    1961-01-01

    Paper chromatographic separations are described by which the minor constituents of biological ashes are separated either into: (Pb) - Mn - Co - (Pb) - Cu - Fe, Mo, Zn; or into: Cu, Mn, Co - Pb - Fe - Mo - Zn.

  5. New Mn II energy levels from STIS-HST spectrum of the HgMn star HD 175640

    CERN Document Server

    Castelli, F; Cowley, C R

    2015-01-01

    The NIST database lists several Mn II lines that were observed in the laboratory but not classified. They cannot be used in spectrum synthesis because their atomic line data are unknown. These lines are concentrated in the 2380-2700 A interval. We aimed to assign energy levels and log gf values to these lines. Semi-empirical line data for Mn II computed by Kurucz were used to synthesize the ultraviolet spectrum of the slow-rotating, HgMn star HD 175640. The spectrum was compared with the high-resolution spectrum observed with the HST-STIS equipment. A UVES spectrum covering the 3050-10000 A region was also examined. We determined a total of 73 new energy levels, 58 from the STIS spectrum of HD 175640 and another 15 from the UVES spectrum. The new energy levels give rise to numerous new computed lines. We have identified more than 50% of the unclassified lines listed in the NIST database and have changed the assignement of another 24 lines. An abundance analysis of the star HD 175640, based on the comparison o...

  6. Chemical spots and their dynamical evolution on HgMn stars

    CERN Document Server

    Korhonen, Heidi; Briquet, Maryline; Gonzalez, Federico; Savanov, Igor

    2010-01-01

    Our recent studies of late B-type stars with HgMn peculiarity revealed for the first time the presence of fast dynamical evolution of chemical spots on their surfaces. These observations suggest a hitherto unknown physical process operating in the stars with radiative outer envelopes. Furthermore, we have also discovered existence of magnetic fields on these stars that have up to now been thought to be non-magnetic. Here we will discuss the dynamical spot evolution on HD 11753 and our new results on magnetic fields on AR Aur.

  7. α MnMoO₄/graphene hybrid composite: high energy density supercapacitor electrode material.

    Science.gov (United States)

    Ghosh, Debasis; Giri, Soumen; Moniruzzaman, Md; Basu, Tanya; Mandal, Manas; Das, Chapal Kumar

    2014-07-28

    A unique and cost effective hydrothermal procedure has been carried out for the synthesis of hexahedron shaped α MnMoO4 and its hybrid composite with graphene using three different weight percentages of graphene. Characterization techniques, such as XRD, Raman and FTIR analysis, established the phase and formation of the composite. The electrochemical characterization of the pseudocapacitive MnMoO4 and the MnMoO4/graphene composites in 1 M Na2SO4 displayed highest specific capacitances of 234 F g(-1) and 364 F g(-1), respectively at a current density of 2 A g(-1). Unlike many other pseudocapacitive electrode materials our prepared materials responded in a wide range of working potentials of (-)1 V to (+)1 V, which indeed resulted in a high energy density without substantial loss of power density. The highest energy densities of 130 Wh kg(-1) and 202.2 Wh kg(-1) were achieved, respectively for the MnMoO4 and the MnMoO4/graphene composite at a constant power delivery rate of 2000 W kg(-1). The synergistic effect of the graphene with the pseudocapacitive MnMoO4 caused an increased cycle stability of 88% specific capacitance retention after 1000 consecutive charge discharge cycles at 8 A g(-1) constant current density, which was higher than the virgin MnMoO4 with 84% specific capacitance retention.

  8. Synthesis and nonlinear optical property of polycrystalline MnTeMoO{sub 6}

    Energy Technology Data Exchange (ETDEWEB)

    Jin, Chengguo [Yibin University, Key Laboratory of Computational Physics of Sichuan Province, Yibin (China); Yibin University, School of Physics and Electronic Engineering, Yibin (China)

    2017-04-15

    Polycrystalline MnTeMoO{sub 6} powder has been synthesized by a new approach that MnO{sub 2} is used as the manganese source. The transformation mechanism of manganese ions in the new approach has been discussed. The nonlinear optical property of polycrystalline MnTeMoO{sub 6} has been investigated, and compared with single-crystalline samples. The transformation Mn{sup 4+} → Mn{sup 2+} may be formed directly without stable intermediates, and TeO{sub 2} may serve as catalyst. The SHG response of polycrystalline MnTeMoO{sub 6} powder is worse than that of single-crystalline powder in the same particle size distribution as its pseudo-size. The results indicate that it should pay special attention with the pseudo-size of polycrystalline powder when the potential nonlinear optical materials are screened by powder second harmonic generation measurements. (orig.)

  9. Synthesis and nonlinear optical property of polycrystalline MnTeMoO6

    Science.gov (United States)

    Jin, Chengguo

    2017-04-01

    Polycrystalline MnTeMoO6 powder has been synthesized by a new approach that MnO2 is used as the manganese source. The transformation mechanism of manganese ions in the new approach has been discussed. The nonlinear optical property of polycrystalline MnTeMoO6 has been investigated, and compared with single-crystalline samples. The transformation Mn4+ → Mn2+ may be formed directly without stable intermediates, and TeO2 may serve as catalyst. The SHG response of polycrystalline MnTeMoO6 powder is worse than that of single-crystalline powder in the same particle size distribution as its pseudo-size. The results indicate that it should pay special attention with the pseudo-size of polycrystalline powder when the potential nonlinear optical materials are screened by powder second harmonic generation measurements.

  10. Determination of MeHg sources to fish in the St. Louis River, MN, USA, using Hg stable isotopes

    Science.gov (United States)

    Mercury contamination in the Great Lakes region has become a prevalent concern due to elevated methylmercury (MeHg) levels in fish. While atmospheric deposition of Hg is ubiquitous, releases from legacy point-sources give rise to numerous Areas of Concern (AOCs) across the Great ...

  11. Internal crack recovery of 20MnMo steel

    Institute of Scientific and Technical Information of China (English)

    韩静涛; 赵钢; 曹起骧

    1997-01-01

    According to the results of physical modelling, SEM and SAM analysis of 20MnMo steel samples, internal cracks of metal parts are recoverable. The motive power of the recovery is atom diffusion and migration from matrix to voids. The recovery process consists of two steps. In the first step, the void area is filled up with a kind of metal mass, beginning from the crack tip. There are many microvoids in the mass with different microstructure from the matrix. In the second step, microvoids decrease in size and number, and the mass microstructure approaches the matrix, with the heating temperature increasing and the holding time prolonging. Recovery tests on rejected heavy forgings are successfully processed. It is believed that the recovery technique is a potential method for improving the internal quality and reducing the production loss and cost of metal products. Similar method can be used to treat other metal construction parts for rescuing them or prolonging their service life. Further research and de

  12. Non-centrosymmetric Rb2Mn2(MoO43

    Directory of Open Access Journals (Sweden)

    Chahira Bouzidi

    2014-07-01

    Full Text Available The title compound, dirubidium dimanganese(II tris(tetraoxomolybdate, Rb2Mn2(MoO43, was prepared by solid-state reactions. The structure can be described as being composed of MnO6 octahedra sharing corners with MoO4 tetrahedra. The three-dimensional framework contains cavities in which the rubidium ions are located. The Rb+ cations are within distorted nine- and 12-vertex polyhedra. The pairs of different Mn2+ and Rb+ cations are each located on threefold rotation axes.. Rb2Mn2(MoO43 is isotypic with compounds of the Cs2M2Mo3O12 (M = Ni, Fe family. A comparative structural description is provided between the structure of the title compound and those of related phases. Differences with structures such as alluaudite are discussed.

  13. Magnetic phase diagrams of {alpha}-MnMoO{sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Ehrenberg, H. [Institute for Materials Science, Darmstadt University of Technology, D-64287 Darmstadt, Petersenstr. 23 (Germany)]. E-mail: ehrenberg@tu-darmstadt.de; Schwarz, B. [Institute for Materials Science, Darmstadt University of Technology, D-64287 Darmstadt, Petersenstr. 23 (Germany); Weitzel, H. [Institute for Materials Science, Darmstadt University of Technology, D-64287 Darmstadt, Petersenstr. 23 (Germany)

    2006-10-15

    Field-induced spin-flop transitions in {alpha}-MnMoO{sub 4} are summarized in magnetic H-T phase diagrams for different directions of the applied magnetic field up to 12T. The antiferromagnetic arrangement in the spin-flop phase is preserved at least up to this field for a field parallel to the easy direction. This high transition field is in contrast to the low one of {alpha}-NiMoO{sub 4} and favours a model, based on dominant antiferromagnetic supersuperexchange couplings in {alpha}-MnMoO{sub 4} over a ferromagnetic Mn{sub 4} ''cluster'' model. The Neel temperature of 9.8(1)K was determined from the corresponding specific-heat anomaly, measured on a single crystal of {alpha}-MnMoO{sub 4}.

  14. Preparation of a novel graphene oxide/Fe-Mn composite and its application for aqueous Hg(II) removal.

    Science.gov (United States)

    Tang, Jingchun; Huang, Yao; Gong, Yanyan; Lyu, Honghong; Wang, Qilin; Ma, Jianli

    2016-10-05

    A novel graphene oxide/Fe-Mn (GO/Fe-Mn) composite was synthesized (molar ratio of Fe/Mn=3/1 and mass ratio of Fe/GO=1/7.5) and investigated for the sorption characteristics and mechanisms of aqueous mercury (Hg(2+)) as well as the biological effects to wheat and rice. Characterization tests showed that Fe-Mn oxides were impregnated onto GO sheets in an amorphous form through oxygen-containing functional groups (i.e., CO, epoxy COC, carboxyl OCO, and CO) and π-π interactions. GO/Fe-Mn possessed large surface area, surface enhanced Raman scattering with more sp(3) defects, and greater thermal stability than GO. XPS analysis revealed that Fe2O3, FeOOH, MnO2, MnOOH, and MnO were the dominant metal oxides in GO/Fe-Mn. Pseudo-second-order kinetic model and Sips isotherm model fitted well with the sorption kinetic and isotherm data. The maximum sorption capacity for mercury was 32.9mg/g. Ligand exchange and surface complexation were the dominant mechanisms for mercury removal. GO/Fe-Mn greatly reduced the bioavailability of mercury to wheat and rice, even promoted the seedling growth. This work suggests that GO/Fe-Mn can be used as an effective and environmental-friendly adsorbent in heavy metal remediation. Copyright © 2016 Elsevier B.V. All rights reserved.

  15. Na1.67Mn2.17(MoO43

    Directory of Open Access Journals (Sweden)

    Chahira Bouzidi

    2014-04-01

    Full Text Available The title compound, disodium dimanganese(II tris[orthomolybdate(VI], was prepared by solid-state reactions. The structure can be described as being composed of Mn2Mo2O14 double-chains that are interconnected by corner-sharing with MoO4 tetrahedra, leading to a three-dimensional framework with channels propagating in [100] and [001] in which the Na+ counter-cations are located. One of these Na sites is located on an inversion centre, one is partially occupied [occupancy 0.341 (9], and one is statistically occupied by Na and Mn in a ratio of 0.829 (5:0.171 (5. Na1.67Mn2.17(MoO43 is isotypic with structures of the Ag2M2(MoO43 (M = Zn, Mg, Co, Mn family. A comparative structural description is provided between the structure of the title compound and those of related phases containing (MXO8n chains (M = Mo, Mn and X = As or M2O10 (M = Mo, Mn, Nb, V dimers.

  16. The peculiar abundance pattern of the new Hg-Mn star HD 30085

    CERN Document Server

    Monier, R; Royer, F; Griffin, R E M

    2015-01-01

    Using high-dispersion, high-quality spectra of HD 30085 obtained with the echelle spectrograph SOPHIE at Observatoire de Haute Provence, we show that this star contains strong lines of the s-process elements Sr II, Y II and Zr II. Line syntheses of the lines yield large overabundances of Sr, Y, Zr which are characteristic of HgMn stars. The Sr-Y-Zr triad of abundances is inverted in HD 30085 compared to that in our solar system. The violation of the odd-even rule suggests that physical processes such as radiative diffusion, chemical fractionation and others must be at work in the atmosphere of HD 30085, and that the atmosphere is stable enough to sustain them.

  17. Theoretical estimation for equilibrium Mo isotope fractionations between dissolved Mo species and the adsorbed complexes on (Fe,Mn)-oxyhydroxides

    Science.gov (United States)

    Tang, M.; Liu, Y.

    2009-12-01

    surface of (Fe,Mn)-oxyhydroxides. We checked the solvation effects, salt effect, temperature effect on the fractionations. Our results show that the solvation effects can dramatically change the fractionation numbers from the ones in gas-phase. For example, the MoO42- - Mo(OH)6 fractionation at 25°C is 0.8‰ for gas-phase but it is changed to 2.0‰ in solution. Our results show that no matter the dominant aqueous species MoO42- is adsorbed on the (Fe,Mn)-oxyhydroxides by the mono-dentate or bi-dentate way, it only can produce less than 1 ‰ isotopic fractionation. The polymerized MoO42- forms (e.g. Mo3O9) also have quite similar fractionation relative to aqueous MoO42-. In another word, the 1.7 - 2‰ Mo isotope offset found between the seawater and the Fe,Mn-oxides, is unlikely caused by the absorption of MoO42- into such oxic sediments. This study provides a base for discussing the mechanism of Mo removal from the seawater.

  18. Intrinsic Ferromagnetism in Mn-Substituted MoS2 Nanosheets Achieved by Supercritical Hydrothermal Reaction.

    Science.gov (United States)

    Tan, Hao; Hu, Wei; Wang, Chao; Ma, Chao; Duan, Hengli; Yan, Wensheng; Cai, Liang; Guo, Peng; Sun, Zhihu; Liu, Qinghua; Zheng, Xusheng; Hu, Fengchun; Wei, Shiqiang

    2017-08-21

    Doping atomically thick nanosheets is a great challenge due to the self-purification effect that drives the precipitation of dopants. Here, a breakthrough is made to dope Mn atoms substitutionally into MoS2 nanosheets in a sulfur-rich supercritical hydrothermal reaction environment, where the formation energy of Mn substituting for Mo sites in MoS2 is significantly reduced to overcome the self-purification effect. The substitutional Mn doping is convincingly evidenced by high-angle annular dark-field scanning transmission electron microscopy and X-ray absorption fine spectroscopy characterizations. The Mn-doped MoS2 nanosheets show robust intrinsic ferromagnetic response with a saturation magnetic moment of 0.05 µB Mn(-1) at room temperature. The intrinsic ferromagnetism is further confirmed by the reversibility of the magnetic behavior during the cycle of incorporating/removing Li codopants, showing the critical role of Mn 3d electronic states in mediating the magnetic interactions in MoS2 nanosheets. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  19. Chemical spots in the absence of magnetic field in the binary HgMn star 66 Eridani

    NARCIS (Netherlands)

    Makaganiuk, V.; Kochukhov, O.; Piskunov, N.; Jeffers, S.V.; Johns-Krull, C. M.; Keller, C.U.; Rodenhuis, M.; Snik, F.; Stempels, H. C.; Valenti, J. A.

    2011-01-01

    Context. According to our current understanding, a subclass of the upper main-sequence chemically peculiar stars, called mercurymanganese (HgMn), is non-magnetic. Nevertheless, chemical inhomogeneities were recently discovered on their surfaces. At the same time, no global magnetic fields stronger t

  20. No detection of large-scale magnetic fields at the surfaces of Am and HgMn stars

    CERN Document Server

    Auriere, M; Lignieres, F; Hui-Bon-Hoa, A; Landstreet, J D; Iliev, I; Donati, J -F; Petit, P; Roudier, T; Theado, S

    2010-01-01

    We investigate the magnetic dichotomy between Ap/Bp and other A-type stars by carrying out a deep spectropolarimetric study of Am and HgMn stars. Using the NARVAL spectropolarimeter at the Telescope Bernard Lyot (Observatoire du Pic du Midi, France), we obtained high-resolution circular polarisation spectroscopy of 12 Am stars and 3 HgMn stars. Using Least Squares Deconvolution (LSD), no magnetic field is detected in any of the 15 observed stars. Uncertaintiies as low as 0.3 G (respectively 1 G) have been reached for surface-averaged longitudinal magnetic field measurements for Am (respectively HgMn) stars. Associated with the results obtained previously for Ap/Bp stars, our study confirms the existence of a magnetic dichotomy among A-type stars. Our data demonstrate that there is at least one order of magnitude difference in field strength between Zeeman detected stars (Ap/Bp stars) and non Zeeman detected stars (Am and HgMn stars). This result confirms that the spectroscopically-defined Ap/Bp stars are the ...

  1. Experimental Investigation and Computer Simulation of Diffusion in Fe-Mo and Fe-Mn-Mo Alloys with Different Optimization Methods

    Science.gov (United States)

    Zheng, Weisen; Ågren, John; Lu, Xiao-Gang; He, Yanlin; Li, Lin

    2017-01-01

    In order to simulate the diffusional phase transformations involving the fcc and bcc phases for microalloyed steels, the diffusion mobilities for fcc and bcc Fe-Mo and Fe-Mn-Mo alloys were experimentally investigated and critically assessed. The diffusion-couple technique was employed to extract the interdiffusion coefficients in Fe-Mo and Fe-Mn-Mo alloys with the Sauer-Freise and Whittle-Green methods. Based on the present experimental interdiffsivities, the mobility parameters for the fcc and bcc phases in the Fe-Mo and Fe-Mn-Mo systems were optimized using the traditional method. Simultaneously, a direct method was developed and utilized to directly fit mobilities to the diffusion profiles rather than the diffusivities in the present work. The satisfactory description of the diffusion behavior in the Fe-Mo and Fe-Mn-Mo systems has confirmed the reliability of the direct method. Particularly, the two sets of diffusion mobilities obtained with both methods could simulate the diffusion phenomenon between the fcc and bcc phases in the Fe-Mo and Fe-Mn-Mo systems successfully.

  2. 超大型20MnMoNbⅣ管板制造%Fabrication of Super-large 20MnMoNbⅣTube-sheet

    Institute of Scientific and Technical Information of China (English)

    韩冰

    2016-01-01

    介绍了超大型20MnMoNb锻件管板的材料要求、锻制工艺、锻件实物的检验数据、锻件拼焊和堆焊的主要工艺措施、如何合理选择无损检测时机及钻孔过程的控制要点,为超大型管板的制造积累了经验.%The material requirements ,forging process ,forging inspection datum ,forging butt welding ,controlling point of overlay welding ,reasonable choosing of non-destructive test time and controlling point of hole drilling for large 20MnMoNb tubesheet are introduced .It accumu-lates the fabrication experience for large tubesheet .

  3. Catalytic oxidation of Hg(0) by MnOx-CeO2/γ-Al2O3 catalyst at low temperatures.

    Science.gov (United States)

    Wang, Pengying; Su, Sheng; Xiang, Jun; You, Huawei; Cao, Fan; Sun, Lushi; Hu, Song; Zhang, Yun

    2014-04-01

    MnOx-CeO2/γ-Al2O3 (MnCe) selective catalytic reduction (SCR) catalysts prepared by sol-gel method were employed for low-temperature Hg(0) oxidation on a fixed-bed experimental setup. BET, XRD and XPS were used to characterize the catalysts. MnCe catalysts exhibited high Hg(0) oxidation activity at low temperatures (100-250 °C) under the simulated flue gas (O2, CO2, NO, SO2, HCl, H2O and balanced with N2). Only a small decrease in mercury oxidation was observed in the presence of 1200 ppm SO2, which proved that the addition of Ce helped resist SO2 poisoning. An enhancing effect of NO was observed due to the formation of multi-activity NOx species. The presence of HCl alone had excellent Hg(0) oxidation ability, while 10 ppm HCl plus 5% O2 further increased Hg(0) oxidation efficiency to 100%. Hg(0) oxidation on the MnCe catalyst surface followed the Langmiur-Hinshelwood mechanism, where reactions took place between the adsorbed active species and adsorbed Hg(0) to form Hg(2+). NH3 competed with Hg(0) for active sites on the catalyst surface, hence inhibiting Hg(0) oxidation. This study shows the feasibility of a single-step process integrating low-temperature SCR and Hg(0) oxidation from the coal combustion flue gas.

  4. Pressure dependent mechanical and thermodynamical properties of Hg0.91Mn0.09Te semiconductor

    Science.gov (United States)

    Varshney, D.; Sapkale, R.; Dagaonkar, G. J.; Varshney, M.

    2011-02-01

    The mechanical, thermodynamical and elastic properties of Hg0.91Mn0.09Te compound are calculated by formulating an effective interionic interaction potential. This potential consists of the long-range Coulomb, three body force parameter, the Hafemeister and Flygare type short-range overlap repulsion extended upto the second neighbor ions and the van der Waals (vdW) interaction. The estimated values of phase transition pressure have revealed reasonably good agreement with the available experimental data on the phase transition pressure P t = 11.5 GPa and the vast volume discontinuity in pressure-volume (PV) phase diagram indicate the structural phase transition from zincblende (B3) to rock salt (B1) structure. Later on, the Poisson's ratio ν, the ratio R S/B of S (Voigt averaged shear modulus) over B (bulk modulus), elastic anisotropy parameter, elastic wave velocity, average wave velocity and Debye temperature as functions of pressure is calculated. From Poisson's ratio and the ratio R S/B it is inferred that Hg0.91Mn0.09Te is brittle in nature in both B3 phase and B1 phase. To our knowledge this is the first quantitative theoretical prediction of the pressure dependence of ductile (brittle) nature of Hg0.91Mn0.09Te compounds and still awaits experimental confirmations.

  5. Sonochemical synthesis, characterization, and electrochemical properties of MnMoO{sub 4} nanorods for supercapacitor applications

    Energy Technology Data Exchange (ETDEWEB)

    Veerasubramani, Ganesh Kumar [Nanomaterials and System Lab, Faculty of Applied Energy System, Science and Engineering College, Jeju National University, Jeju 690-756 (Korea, Republic of); Department of Mechatronics Engineering, Jeju National University, Jeju 690-756 (Korea, Republic of); Krishnamoorthy, Karthikeyan; Sivaprakasam, Radhakrishnan [Nanomaterials and System Lab, Department of Mechanical Engineering, Jeju National University, Jeju 690-756 (Korea, Republic of); Kim, Sang Jae, E-mail: kimsangj@jejunu.ac.kr [Nanomaterials and System Lab, Department of Mechanical Engineering, Jeju National University, Jeju 690-756 (Korea, Republic of); Department of Mechatronics Engineering, Jeju National University, Jeju 690-756 (Korea, Republic of)

    2014-10-15

    In this article, we reported the preparation of manganese molybdate (MnMoO{sub 4}) nanorods by a facile sonochemical method and investigated its electrochemical properties for supercapacitor applications. The microstructure, surface morphology and composition were characterized by using field emission scanning electron microscope (FE-SEM), high resolution-transmission electron microscopy (HR-TEM), X-ray diffraction analysis (XRD), Raman spectroscopy and X-ray photo electron microscopy (XPS). The cyclic voltammetry (CV) curves of sonochemically synthesized α-MnMoO{sub 4} nanorods revealed the presence of redox pairs suggesting the pseudocapacitive nature of MnMoO{sub 4}. A maximum specific capacitance of the α-MnMoO{sub 4} nanorods was about 168.32 F g{sup −1} as observed from the galvanostatic charge–discharge (GCD) analysis at a constant current density of 0.5 mA cm{sup −2}. Long term cyclic stability study revealed that about 96% of initial capacitance was retained after 2000 cycles. - Highlights: • MnMoO{sub 4} nanorods were synthesized by sonochemical method. • FE-SEM studies show the rod like morphology of MnMoO{sub 4}. • XRD studies show the presence of monoclinic phase of α-MnMoO{sub 4}. • Specific capacitance of 168.32 F g{sup −1} was achieved using charge–discharge analysis.

  6. Structure cristalline de type alluaudite KNa5Mn3(MoO46

    Directory of Open Access Journals (Sweden)

    Chahira Bouzidi

    2015-01-01

    Full Text Available The new phase potassium pentasodium trimanganese hexakis(molybdate, KNa5Mn3Mo6O24, has been synthesized using solid-state methods. The structure is composed of M2O10 (M = Mn, Na dimers and MoO4 tetrahedra (point group symmetry 2 sharing corners and forming layers parallel to (100, which are linked via common corners of another type of MO4 tetrahedra, forming a three-dimensional structure with two types of large channels along [001] in which two types of Na+ cations (one with site symmetry 2, one with -1 and K+ cations (site symmetry 2, half-occupation are located. Mn2+ and the third type of Na+ cations are located at the same site M with occupancies of 0.75 and 0.25, respectively. A comparative structural description is provided between the structure of the title compound and those of the related phases Cu1.35Fe3(PO43 and NaAgFeMn2(PO43.

  7. B -meson decay constants from <mn>2mn>+>1mn> -flavor lattice QCD with domain-wall light quarks and relativistic heavy quarks

    Energy Technology Data Exchange (ETDEWEB)

    Christ, N. H.; Flynn, J. M.; Izubuchi, T.; Kawanai, T.; Lehner, C.; Soni, A.; Van de Water, R. S.; Witzel, O.

    2015-03-01

    We calculate the B-meson decay constants fB, fBs, and their ratio in unquenched lattice QCD using domain-wall light quarks and relativistic b quarks. We use gauge-field ensembles generated by the RBC and UKQCD collaborations using the domain-wall fermion action and Iwasaki gauge action with three flavors of light dynamical quarks. We analyze data at two lattice spacings of amo>≈>0.11mn>, 0.086 fm with unitary pion masses as light as Mπmo>≈>290mn>MeV; this enables us to control the extrapolation to the physical light-quark masses and continuum. For the b quarks we use the anisotropic clover action with the relativistic heavy-quark interpretation, such that discretization errors from the heavy-quark action are of the same size as from the light-quark sector. We renormalize the

  8. Generator of {sup 99m} Tc with MnO{sub 2} as support of {sup 99} Mo; Generador de {sup 99m} Tc con MnO{sub 2} como soporte del {sup 99}Mo

    Energy Technology Data Exchange (ETDEWEB)

    Granados C, F.; Serrano G, J. [Departamento de Quimica, Instituto Nacional de Investigaciones Nucleares, A.P. 18-1027, 11801 Mexico D.F. (Mexico)

    2002-07-01

    The generator of {sup 99m} Tc with MnO{sub 2} as support of {sup 99} Mo was studied. By mean of static experiments the retention of {sup 99} Mo in MnO{sub 2} in function of the stirring time and of the p H value of the solution of {sup 99} Mo. It was found that the {sup 99} Mo presents 100% of retention in MnO{sub 2} in the rank of p H 3-11 and the balance was reached before of 10 minutes. In dynamic conditions the retention of {sup 99} Mo in MnO{sub 2} at p H=5 was also higher: 99.72%. The generated {sup 99m} Tc can be separated from {sup 99} Mo, adsorbed in MnO{sub 2} packed in the column, using distilled water at p H=5 or NaCl solution at 0.9%. With saline solution the elution yields were greater than 80% and only an aliquot of 5 ml was necessary for obtaining this yield. The better results were obtained when the column was packed with 1 g of MnO{sub 2}. The water and the saline solution were passed through of the column with a flux of 1.25 ml/min. (Author)

  9. Tensile properties and fracture surface of 07MnNiCrMoVDR steel welded joint at low temperature

    Institute of Scientific and Technical Information of China (English)

    Zhang Lihong; Chen Furong; Xie Ruijun

    2009-01-01

    The tensile properties and fracture surfuce of 07MnNiCrMoVDR steel welded joint at low temperature have been studied by universal testing machine and scanning electron microscope. The results show that the tensile properties of 07MnNiCrMoVDR steel welded joint are greatly affected by temperature. Tensile strength and yield strength of 07MnNiCrMoVDR steel welded joint increase, bat elongation and reduction of area decrease with temperature decreasing. The macro-fracture of 07 MnNiCrMoVDR steel welded joint exhibits that the shear lip is not significant and micro-fracture makes up of dimpled fracture and tear fracture, and dimple becomes tiny and uniform with temperature decreasing.

  10. Chemical spots in the absence of magnetic field in the binary HgMn star 66 Eridani

    CERN Document Server

    Makaganiuk, V; Piskunov, N; Jeffers, S V; Johns-Krull, C M; Keller, C U; Rodenhuis, M; Snik, F; Stempels, H C; Valenti, J A

    2011-01-01

    According to our current understanding, a subclass of the upper main sequence chemically peculiar stars, called mercury-manganese (HgMn), is non-magnetic. Nevertheless, chemical inhomogeneities were recently discovered on their surfaces. At the same time, no global magnetic fields stronger than 1-100 G are detected by modern studies. The goals of our study are to search for magnetic field in the HgMn binary system 66 Eri and to investigate chemical spots on the stellar surfaces of both components. Our analysis is based on high quality spectropolarimetric time-series observations obtained during 10 consecutive nights with the HARPSpol instrument at the ESO 3.6-m telescope. To increase the sensitivity of the magnetic field search we employed a least-squares deconvolution (LSD). We used spectral disentangling to measure radial velocities and study line profile variability. Chemical spot geometry was reconstructed using multi-line Doppler imaging. We report a non-detection of magnetic field in 66 Eri, with error ...

  11. Determination of Fe, Hg, Mn, and Pb in three-rings of poplar (Populus alba L.) by U-shaped DC arc

    Science.gov (United States)

    Marković, D. M.; Novović, I.; Vilotić, D.; Ignjatović, Lj.

    2007-09-01

    The U-shaped DC arc with aerosol supply was applied for the determination of Fe, Hg, Mn, and Pb in poplar (Populus alba L.) tree-rings. By optimization of the operating parameters and by selection of the most appropriate signal integration time (20 s for Fe, Mn, and Pb and 30 s for Hg), the obtained limits of detection for Fe, Hg, Mn, and Pb are 5.8, 2.6, 1.6, and 2.0 ng/ml, respectively. The detection limits achieved by this method for Fe, Hg, Mn, and Pb are comparable with the detection limits obtained for these elements by such methods as inductively coupled plasma-atomic emission spectrometry (ICP-AES), direct coupled plasmatomic emission spectrometry (DCP-AES), and microwave-induced plasma-atomic emission spectrometry (MIP-AES). We used the tree-rings of poplar from two different locations. The first one is in the area close to the power plant “Nikola Tesla” TENT A, Obrenovac, while the other one is in the urban area of Novi Sad. In almost all cases, samples from the location at Obrenovac registered elevated average concentrations of Fe, Hg, Mn, and Pb in the tree-rings of poplar.

  12. Dynamical evolution of titanium, strontium, and yttrium spots on the surface of the HgMn star HD 11753

    CERN Document Server

    Briquet, M; Gonzalez, J F; Hubrig, S; Hackman, T

    2010-01-01

    Aims. We gathered about 100 high-resolution spectra of three typical HgMn (mercury-manganese) stars, HD 11753, HD 53244, and HD 221507, to search for slowly pulsating B-like pulsations and surface inhomogeneous distribution of various chemical elements. Methods. Classical frequency analysis methods were used to detect line profile variability and to determine the variation period. Doppler imaging reconstruction was performed to obtain abundance maps of chemical elements on the stellar surface. Results. For HD 11753, which is the star with the most pronounced variability, distinct spectral line profile changes were detected for Ti, Sr, Y, Zr, and Hg, whereas for HD 53244 and HD 221507 the most variable line profiles belong to the elements Hg and Y, respectively. We derived rotation periods for all three stars from the variations of radial velocities and equivalent widths of spectral lines belonging to inhomogeneously distributed elements: P_rot (HD 11753)=9.54 d, P_rot (HD 53244)=6.16 d, and P_rot (HD 221507)=...

  13. Electron paramagnetic resonance studies in HgMo sub 6 S sub 8 doped with Cu sup 2 sup + : evidence for cationic mobility

    CERN Document Server

    Kadam, R M; Iyer, R M; Gopalakrishnan, I K; Yakhmi, J V

    1997-01-01

    Some of the Chevrel phase compounds are reported to exhibit unusual cationic mobilities, particularly those with transition metals. EPR evidence is presented for mobile Cu sup 2 sup + ions in Cu sup 2 sup + -doped HgMo sub 6 S sub 8. Evidence is also obtained for the existence of Hg sup + ions, giving possible support for the model correlating the site change with the reaction A sup 2 sup + + e sup -reversible A sup + during ionic conductivity. (author)

  14. Fabrication of Alternate Stacking MnO2/MoS2 Layered Nanohybrid by a Sonochemistry Technology

    Institute of Scientific and Technical Information of China (English)

    SU Zhi-Kui; CUI Yan-Hua; TANG Xiu-Hua; ZHOU Qing; LIU Zong-Huai

    2008-01-01

    Layered manganese oxide was delaminated in a tetramethylammonium hydroxide by sonicating treatment for hated MnO2 colloid by ultrasonic treatment, and alternate stacking MnO2/MoS2 nanohybrid with a novel layered structure was fabricated by using a sonochemistry technology. A new hybridization method between two kinds of inorganic nanosheets with the same charge character was developed.

  15. Growth of NiCo2O4@MnMoO4 Nanocolumn Arrays with Superior Pseudocapacitor Properties.

    Science.gov (United States)

    Cui, Chunyu; Xu, Jiantie; Wang, Lei; Guo, Di; Mao, Minglei; Ma, Jianmin; Wang, Taihong

    2016-04-06

    Three-dimensional heterostructured NiCo2O4@MnMoO4 nanocolumn arrays (NCAs) on Ni foam were first fabricated through an improved two-step hydrothermal process associated with a successive annealing treatment. The hybrid NiCo2O4@MnMoO4 electrode exhibited remarkable pseudocapacitor property with high initial mass specific capacitance of 1705.3 F g(-1) at 5 mA cm(-2), and retained 92.6% after 5000 cycles, compared to the bare NiCo2O4 electrode with 839.1 F g(-1) and 90.9%. The excellent capacitive property of the NiCo2O4@MnMoO4 hydrid was attributed to its high-electron/ion-transfer rate, large electrolyte infiltrate area, and more electroactive reaction sites.

  16. Distortion, interaction, and conceptual DFT perspectives of MO4-alkene (M = Os, Re, Tc, Mn) cycloadditions.

    Science.gov (United States)

    Ess, Daniel H

    2009-02-20

    The reaction pathways (including the transition states) of ethylene addition to osmium tetroxide (OsO(4), and amine ligated), rhenate (ReO(4)(-)), technetate (TcO(4)(-)), and permanganate (MnO(4)(-)) have been studied by qualitative and quantitative analyses. Distortion/interaction and absolutely localized energy decomposition analyses provide new insights into why the (3 + 2) pathway is highly preferred over the (2 + 2) pathway, the origin of rate enhancement from ligated base, and reactivity differences between OsO(4), ReO(4)(-), TcO(4)(-), and MnO(4)(-). The (2 + 2) transition state has a much larger barrier than the (3 + 2) transition state because (1) the Os-O bond is stretched significantly resulting in a larger distortion energy (DeltaE(d)(double dagger)) value and (2) the transition state interaction energy (DeltaE(i)(double dagger)) is destabilizing due to large exchange repulsions overwhelming stabilizing charge-transfer terms. Base ligation lowers osmium tetroxide and ethylene distortion energies due to the ground-state O-Os-O angle being predistorted from 110 degrees to 103 degrees. Because MO(4) distortion energies are comparable, reactivity differences between OsO(4), ReO(4)(-), TcO(4)(-), and MnO(4)(-) is shown to be a function of ethylene to MO(4) charge-transfer. This interaction also dictates the position of the transition state along the reaction coordinate and corresponds to the onset of a stabilizing DeltaE(i)(double dagger) value. The conceptual DFT hardness profile and hardness response show that the (3 + 2) reaction pathway may be classified as an "allowed" pathway while the (2 + 2) reaction coordinate is best designated as "forbidden".

  17. Measurement of target and double-spin asymmetries for the e<mo>→>p<mo>→mo><mo>→mo>eπ<mo>+mo><mo>(n)> reaction in the nucleon resonance region at low Q<mn>2mn>

    Energy Technology Data Exchange (ETDEWEB)

    Zheng, X.; Adhikari, K. P.; Bosted, P.; Deur, A.; Drozdov, V.; El Fassi, L.; Kang, Hyekoo; Kovacs, K.; Kuhn, S.; Long, E.; Phillips, S. K.; Ripani, M.; Slifer, K.; Smith, L. C.; Adikaram, D.; Akbar, Z.; Amaryan, M. J.; Anefalos Pereira, S.; Asryan, G.; Avakian, H.; Badui, R. A.; Ball, J.; Baltzell, N. A.; Battaglieri, M.; Batourine, V.; Bedlinskiy, I.; Biselli, A. S.; Briscoe, W. J.; Bültmann, S.; Burkert, V. D.; Carman, D. S.; Celentano, A.; Chandavar, S.; Charles, G.; Chen, J. -P.; Chetry, T.; Choi, Seonho; Ciullo, G.; Clark, L.; Colaneri, L.; Cole, P. L.; Compton, N.; Contalbrigo, M.; Crede, V.; D' Angelo, A.; Dashyan, N.; De Vita, R.; De Sanctis, E.; Djalali, C.; Dodge, G. E.; Dupre, R.; Egiyan, H.; El Alaoui, A.; Elouadrhiri, L.; Eugenio, P.; Fanchini, E.; Fedotov, G.; Fersch, R.; Filippi, A.; Fleming, J. A.; Gevorgyan, N.; Ghandilyan, Y.; Gilfoyle, G. P.; Giovanetti, K. L.; Girod, F. X.; Gleason, C.; Golovach, E.; Gothe, R. W.; Griffioen, K. A.; Guidal, M.; Guler, N.; Guo, L.; Hanretty, C.; Harrison, N.; Hattawy, M.; Hicks, K.; Holtrop, M.; Hughes, S. M.; Ilieva, Y.; Ireland, D. G.; Ishkhanov, B. S.; Isupov, E. L.; Jenkins, D.; Jiang, H.; Jo, H. S.; Joosten, S.; Keller, D.; Khachatryan, G.; Khandaker, M.; Kim, A.; Kim, W.; Klein, F. J.; Kubarovsky, V.; Lanza, L.; Lenisa, P.; Livingston, K.; MacGregor, I. J. D.; Markov, N.; McKinnon, B.; Mirazita, M.; Mokeev, V.; Movsisyan, A.; Munevar, E.; Munoz Camacho, C.; Murdoch, G.; Nadel-Turonski, P.; Net, L. A.; Ni, A.; Niccolai, S.; Niculescu, G.; Niculescu, I.; Osipenko, M.; Ostrovidov, A. I.; Paolone, M.; Paremuzyan, R.; Park, K.; Pasyuk, E.; Peng, P.; Pisano, S.; Pogorelko, O.; Price, J. W.; Puckett, A. J. R.; Raue, B. A.; Rizzo, A.; Rosner, G.; Rossi, P.; Roy, P.; Sabatié, F.; Salgado, C.; Schumacher, R. A.; Sharabian, Y. G.; Skorodumina, Iu.; Smith, G. D.; Sokhan, D.; Sparveris, N.; Stankovic, I.; Strakovsky, I. I.; Strauch, S.; Taiuti, M.; Tian, Ye; Ungaro, M.; Voskanyan, H.; Voutier, E.; Walford, N. K.; Watts, D. P.; Wei, X.; Weinstein, L. B.; Wood, M. H.; Zachariou, N.; Zhang, J.; Zonta, I.

    2016-10-01

    We report measurements of target- and double-spin asymmetries for the exclusive channel e<mo>→>p<mo>→mo><mo>→mo>eπ<mo>+mo><mo>(n)> in the nucleon resonance region at Jefferson Lab using the CEBAF Large Acceptance Spectrometer (CLAS). These asymmetries were extracted from data obtained using a longitudinally polarized NH3 target and a longitudinally polarized electron beam with energies 1.1, 1.3, 2.0, 2.3, and 3.0 GeV. The new results are consistent with previous CLAS publications but are extended to a low Q2 range from 0.0065 to 0.35 (GeV/c)2. The Q2 access was made possible by a custom-built Cherenkov detector that allowed the detection of electrons for scattering angles as low as 6 degrees. These results are compared with the unitary isobar models JANR and MAID, the partial-wave analysis prediction from SAID, and the dynamic model DMT. In many kinematic regions our results, in particular results on the target asymmetry, help to constrain the polarization-dependent components of these models.

  18. DYNAMIC TENSILE BEHAVIOR OF 5CrMnMo AT ELEVATED TEMPERATURES

    Institute of Scientific and Technical Information of China (English)

    W. Huang; X. Nie; X. Zan; Y.M. Xia

    2004-01-01

    A new experimental technique has been developed for the performance of high temperature, high-strain rate tensile experiments in the self-designed tensile impact apparatus. This technique uses rapid contact heating method to heat the specimen to the desired temperature, thus avoids a significant temperature rise in incident and transmitted bars, and at the same time it is capable of retaining a nearly homogeneous temperature field within the specimen. As an illustration of its application, the hightemperature response of the forging die steel 5CrMnMo at high strain rates has been examined. Stress-strain curves are obtained for this material at strain rates ranging from 230s-1 to 1200s-1 and at temperature ranging from 25 to 600℃, respectively.For comparison, quasi-static experiments are performed over a slightly smaller range of temperatures.

  19. Insulator-Metal Transition due to La Doping in Double Perovskite Sr2MnMoO6

    Institute of Scientific and Technical Information of China (English)

    刘晓峻; 黄巧建; 徐胜; 张淑仪; 罗爱华

    2004-01-01

    Resistivity, thermal diffusivity, lattice and magnetic properties of double perovskite Sr2-xLaxMnMoO6 are investigated with systematic change of La doping concentration x from 0.0 to 0.4. The insulator to metal phase transition is observed with increasing x above 0.3, suggesting that the extra electrons via substitution of La3+for Sr2+ ions occupy mainly the conduction Mo-4d band. According to the insulator to metal phase transition,the thermal diffusivity of Sr2-xLaxMnMoO6 enhances from 0.33cm2/s at x = 0.0 to 0.49cm2/s at x = 0.4. We further investigate the La doping effects on the lattice and magnetic properties.

  20. The HgMn Binary Star Phi Herculis: Detection and Properties of the Secondary and Revision of the Elemental Abundances of the Primary

    CERN Document Server

    Zavala, R T; Hummel, C A; Gulliver, A F; Caliskan, H; Armstrong, J T; Hutter, D J; Johnston, K J; Pauls, T A

    2006-01-01

    Observations of the Mercury-Manganese star Phi Herculis with the Navy Prototype Optical Interferometer (NPOI) conclusively reveal the previously unseen companion in this single-lined binary system. The NPOI data were used to predict a spectral type of A8V for the secondary star Phi Her B. This prediction was subsequently confirmed by spectroscopic observations obtained at the Dominion Astrophysical Observatory. Phi Her B is rotating at 50 +/-3 km/sec, in contrast to the 8 km/sec lines of Phi Her A. Recognizing the lines from the secondary permits one to separate them from those of the primary. The abundance analysis of Phi Her A shows an abundance pattern similar to those of other HgMn stars with Al being very underabundant and Sc, Cr, Mn, Zn, Ga, Sr, Y, Zr, Ba, Ce, and Hg being very overabundant.

  1. Mechanism of a strongly anisotropic MoIII-CN-MnII spin-spin coupling in molecular magnets based on the [Mo(CN)(7)](4-) heptacyanometalate: a new strategy for single-molecule magnets with high blocking temperatures.

    Science.gov (United States)

    Mironov, Vladimir S; Chibotaru, Liviu F; Ceulemans, Arnout

    2003-08-13

    Unusual spin coupling between Mo(III) and Mn(II) cyano-bridged ions in bimetallic molecular magnets based on the [Mo(III)(CN)(7)](4-) heptacyanometalate is analyzed in terms of the superexchange theory. Due to the orbital degeneracy and strong spin-orbit coupling on Mo(III), the ground state of the pentagonal-bipyramidal [Mo(III)(CN)(7)](4-) complex corresponds to an anisotropic Kramers doublet. Using a specially adapted kinetic exchange model we have shown that the Mo(III)-CN-Mn(II) superexchange interaction is extremely anisotropic: it is described by an Ising-like spin Hamiltonian JS(z)(Mo) S(z)(Mn) for the apical pairs and by the J(z)S(z)(Mo) S(z)(Mn) + J(xy)(Sx(Mo) Sx(Mn) + Sy(Mo) Sy(Mn)) spin Hamiltonian for the equatorial pairs (in the latter case J(z) and J(xy) can have opposite signs). This anisotropy resulted from an interplay of several Ising-like (Sz(Mo) Sz(Mn)) and isotropic (S(Mo)S(Mn)) ferro- and antiferromagnetic contributions originating from metal-to-metal electron transfers through the pi and sigma orbitals of the cyano bridges. The Mo(III)-CN-Mn(II) exchange anisotropy is distinct from the anisotropy of the g-tensor of [Mo(III)(CN)(7)](4-); moreover, there is no correlation between the exchange anisotropy and g-tensor anisotropy. We indicate that highly anisotropic spin-spin couplings (such as the Ising-like JS(z)(Mo) S(z)(Mn)) combined with large exchange parameters represent a very important source of the global magnetic anisotropy of polyatomic molecular magnetic clusters. Since the total spin of such clusters is no longer a good quantum number, the spin spectrum pattern can differ considerably from the conventional scheme described by the zero-field splitting of the isotropic spin of the ground state. As a result, the spin reorientation barrier of the magnetic cluster may be considerably larger. This finding opens a new way in the strategy of designing single-molecule magnets (SMM) with unusually high blocking temperatures. The use of

  2. Determination of the Solid/Liquid Interface Shape and Resultant Radial Homogeneity in Directionally Solidified Hg(0.89)Mn(0.11)Te

    Science.gov (United States)

    Price, M. W.; Scripa, R. N.; Lehoczky, S. L.; Szofran, F. R.; Hanson, B.

    1999-01-01

    Directional solidification and interrupted directional solidification experiments were used to determine tile shape of the solid/liquid interface and the resultant radial homogeneity in Hg(0.89)Mg(0.11)Te. For directionally solidified samples solidified at a rate of 0.09 microns/sec in a thermal gradient of 83 C/cm, a maximum of 0.006 molar percent MnTe radial variation across the Hg0.89)Mn(0.11)Te boules at specific locations was determined using an FTIR technique. This FTIR evaluation of the radial homogeneity also indicated an asymmetrical, convex interface shape during solidification. The asymmetrical, convex shape of the growth interface was confirmed by interrupted directional solidification experiments. These were performed under the same growth conditions as the normally completed directional solidification experiments except that the samples were quenched before the final growth transient was reached. In these experiments, etching and scanning X-ray fluorescence were used to reveal the shape of the solid/liquid interface. Microprobe analysis of composition gradients across the interface was used to confirm the authors' previous work in evaluating the segregation coefficient of Hg(0.89)Mn(0.11)Te alloy. Microprobe analysis of the interface region of the interrupted growth sample revealed a dendritic structure containing secondary and tertiary dendritic arms.

  3. Survey of trace elements (Al, As, Cd, Cr, Co, Hg, Mn, Ni, Pb, Se, and Si) in retail samples of flavoured and bottled waters.

    Science.gov (United States)

    Barroso, M F; Ramos, S; Oliva-Teles, M T; Delerue-Matos, C; Sales, M G F; Oliveira, M B P P

    2009-01-01

    Concentrations of eleven trace elements (Al, As, Cd, Cr, Co, Hg, Mn, Ni, Pb, Se, and Si) were measured in 39 (natural and flavoured) water samples. Determinations were performed using graphite furnace electrothermetry for almost all elements (Al, As, Cd, Cr, Co, Mn, Ni, Pb, and Si). For Se determination hydride generation was used, and cold vapour generation for Hg. These techniques were coupled to atomic absorption spectrophotometry. The trace element content of still or sparkling natural waters changed from brand to brand. Significant differences between natural still and natural sparkling waters (p differences between flavoured and natural waters. The concentration of each element was compared with the presence of flavours, preservatives, acidifying agents, fruit juice and/or sweeteners, according to the labelled composition. It was shown that flavoured waters generally increase the trace element content. The addition of preservatives and acidifying regulators had a significant influence on Mn, Co, As and Si contents (p difference in Mn, Co, Se and Si content.

  4. A rare 3D chloro-laced Mn(II) metal-organic framework to show sensitive probing effect to Hg2+

    Science.gov (United States)

    Ming, Mei; Bai, Na

    2017-10-01

    Two 3D Mn(II) metal-organic frameworks (MOFs), [Mn(L-Cl)(DMA)](H2O) (1) and Mn(L-CH3)(DMA) (2) (H2L-Cl = 2,2'-dichloro-4,4'-azodibenzoic acid, H2L-CH3 = 2,2'-dimethyl-4,4'-azodibenzoic acid) were synthesized under similar solvothermal condition. Both MOFs crystallize in the orthorhombic system and show the 3D rod-packing networks in 2-fold interpenetrated pattern with sra topology. Due to the different substituent laces of MOFs (-Cl vs -CH3), only MOF 1 shows highly selective and sensitive fluorescence sensing effect for detecting Hg2+ ion.

  5. A pure inorganic 1D chain based on {Mo8O28} clusters and Mn(II) ions: [Mn(H2O)2Mo8O28 ] n 6 n -

    Science.gov (United States)

    Zhang, Xiaofen; Yan, Yonghong; Wu, Lizhou; Yu, Chengxin; Dong, Xinbo; Hu, Huaiming; Xue, Ganglin

    2016-01-01

    A new pure inorganic polymer, (NH4)6n[Mn(H2O)2Mo8O28)]n(H2O)2n(1), has been synthesized and characterized by elemental analyses, IR spectrum, UV-vis absorption spectra, TG-DSC and electrochemical studies. In 1, [Mo8O28]8- anions act as tetradentate ligands and are alternately linked by Mn(H2O)2 2 + ions into a one-dimensional chain structure. It is interesting that 1 represents the first example of pure inorganic-inorganic hybrid based on octamolybdate and transition metal ions. Moreover, it was indicated that 1 had definite catalytic activities on the probe reaction of benzyl alcohol oxidation to benzaldehyde with H2O2.

  6. Sol-Gel Synthesis of LaMO3 (M = Cr, Mn, Fe, Co, Ni) Nanocrystalline Powders

    Institute of Scientific and Technical Information of China (English)

    Chen Zhanheng; Xing Xianran; Dai Jing; Huang Xiaowei; Li Hongwei

    2004-01-01

    Sol-gel synthesis of LaMO3 ( M = Cr, Mn, Fe, Co, Ni) nanocrystalline Powders was investigated. DSC measurement shows that precursors decomposed at about 403 K and 620 K to bum out of N, C, and H. The calcined samples at 1073 K were determined by XRD to be single phase. SEM observation shows that the prepared samples are nanocrystalline powders in broad sense. The average grain size of LaM'O3 (M'= Cr, Mn, Fe, Ni) is 150 ~700 nm,and the grain size of LaCoO3 is about 30 nm.

  7. A search for pulsations in the HgMn star HD 45975 with CoRoT photometry and ground-based spectroscopy

    CERN Document Server

    Morel, T; Auvergne, M; Alecian, G; Ghazaryan, S; Niemczura, E; Fossati, L; Lehmann, H; Hubrig, S; Ulusoy, C; Damerdji, Y; Rainer, M; Poretti, E; Borsa, F; Scardia, M; Schmid, V S; Van Winckel, H; De Smedt, K; Papics, P I; Gameiro, J F; Waelkens, C; Fagas, M; Kaminski, K; Dimitrov, W; Baglin, A; Michel, E; Dumortier, L; Fremat, Y; Hensberge, H; Jorissen, A; Van Eck, S

    2013-01-01

    The existence of pulsations in HgMn stars is still being debated. To provide the first unambiguous observational detection of pulsations in this class of chemically peculiar objects, the bright star HD 45975 was monitored for nearly two months by the CoRoT satellite. Independent analyses of the light curve provides evidence of monoperiodic variations with a frequency of 0.7572 c/d and a peak-to-peak amplitude of ~2800 ppm. Multisite, ground-based spectroscopic observations overlapping the CoRoT observations show the star to be a long-period, single-lined binary. Furthermore, with the notable exception of mercury, they reveal the same periodicity as in photometry in the line moments of chemical species exhibiting strong overabundances (e.g., Mn and Y). In contrast, lines of other elements do not show significant variations. As found in other HgMn stars, the pattern of variability consists in an absorption bump moving redwards across the line profiles. We argue that the photometric and spectroscopic changes are...

  8. Effect of Mn on hardenability of 25CrMo axle steel by an improved end-quench test

    Directory of Open Access Journals (Sweden)

    Zhang Yutuo

    2012-11-01

    Full Text Available With the sixth large-scale railway speed-up, the quality of the axles is essential to the safety of the locomotive. According to the high-speed axle technical standard for the control of alloy elements in axle steel, optimization experiments of 25CrMo steel composition were performed by vacuum inductive melting. In order to study the hardenability of high-speed rail axles, an improved end-quench test was put forward. The advantage is that it enables the heat to transfer along the axial direction, thus avoiding edge effects. The hardenability of 25CrMo axle steels with Mn content of 0.60wt.% and 0.80wt.% was investigated mainly by means of optical microscopy and hardness tests. The experimental results indicate that the Mn has a pronounced effect on the hardenability of the steel. With an increase in Mn content from 0.60wt.% and 0.80wt.%, the hardenability of 25CrMo axle steel increases and the hard microstructure is maintained at an increasing distance from the quenched end. From the surface of the water quenched end to the center of the sample, the microstructure is martensite, martensite with bainite, and bainite.

  9. Competition between Band Filling and Steric Effect in Ordered Double Perovskites Sr2-xLaxMnMoO6

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    The ordered double perovskites, Sr2-xLaxMnMoO6, were prepared by sol-gel reaction. Structural, magnetic, and electrical properties were investigated for a series of ordered double perovskites Sr2-xLaxMnMoO6 (0≤x≤1). The compounds have a monoclinic structure (space group P21/n) and the cell volume expands monotonically with La doping. The TC and the magnetic moment rise and the cusp-like transition temperature below which the magnetic frustration occurs shifts to high temperature as x increases. With La doping, electrical resistivity of Sr2-xLaxMnMoO6 decreases only at low doping levels (x≤0.2); while at high doping levels (0.8≤x≤1), electrical resistivity tends to increase greatly. The results suggest that the competition between band filling effect and steric effect coexists in the whole doping range, and the formation of ferrimagnetic interactions is not simply at the expense of antiferromagnetic interactions.

  10. 20CrMnMo钢稀土渗碳研究%Study on RE Carburizing of 20CrMnMo Steel

    Institute of Scientific and Technical Information of China (English)

    徐建军; 杜晓东

    2012-01-01

    RE carburization was carried out on 20CrMnMo steel. The carburizing kinetics of carburizing depth was dealed with, the microstructure of the carburized layer was observed, the hardness and abrasion resistance of the carburized layer were examined. The results show that a large amount of dispersed granular carbides precipitated in the carburized layer of 20CrMnMo steel RE carburized. The microstructure of surface layer after directly quenching consists of acicular martensite, fine granular carbides and a little residual austenite. The test results showed 10 persent improvement in hardness, 32 persent improvement in abrasion resistance,The touching fatigue life is sharply improved too.%采用稀土渗碳工艺对20CrMnMo钢进行渗碳处理,研究了渗层增厚的动力学、渗碳层组织和性能.结果表明:稀土渗碳层中沉淀析出了大量弥散分布的粒状碳化物,淬火后表层组织为针状马氏体、大量细小颗粒碳化物、少量残余奥氏体.渗碳层的硬度与传统工艺相比提高了10%,耐磨性提高了32%,接触疲劳寿命也有大幅提高.

  11. Synthesis, Structure and Characterization of Three Metal Molybdate Hydrates: Fe(H2O)2(MoO4)2·H3O, NaCo2(MoO4)2(H3O2)and Mn2(MoO4)3·2H3O

    Institute of Scientific and Technical Information of China (English)

    YU Yang; FENG Shou-hua; LIU Dan; HU Wei-wei; LI Jia; PENG Yu; ZHOU Qi; YANG Fen; LI Guang-hua; SHI Zhan

    2012-01-01

    Three metal molybdate hydrates,Fe(H2O)2(MoO4)2·H3O(FeMo),NaCo2(MoO4)2(H3O2)(CoMo)and Mn2(MoO4)3·2H3O(MnMo),were synthesized by the mixed-solvent-thermal methods and characterized by singlecrystal X-ray diffraction.X-Ray photoelectron spectroscopy and bond-valence sums were applied to confirming the valance of Fe,Co,Mn and Mo.Thermo-gravimetric analysis and X-ray powder diffraction measurements indicate that the samples were converted to different structural compounds upon heating in air at 600 ℃ for 1 h.The magnetic properties of these compounds were studied.The dominant magnetic interactions are antiferromagnetic in nature.However,different synthesis conditions led to the diversity of magnetic properties of compound CoMo.

  12. B -meson decay constants from <mn>2mn>+>1mn> -flavor lattice QCD with domain-wall light quarks and relativistic heavy quarks

    Energy Technology Data Exchange (ETDEWEB)

    Christ, N. H.; Flynn, J. M.; Izubuchi, T.; Kawanai, T.; Lehner, C.; Soni, A.; Van de Water, R. S.; Witzel, O.

    2015-03-01

    We calculate the B-meson decay constants fB, fBs, and their ratio in unquenched lattice QCD using domain-wall light quarks and relativistic b quarks. We use gauge-field ensembles generated by the RBC and UKQCD collaborations using the domain-wall fermion action and Iwasaki gauge action with three flavors of light dynamical quarks. We analyze data at two lattice spacings of amo>≈>0.11mn>, 0.086 fm with unitary pion masses as light as Mπmo>≈>290mn>MeV; this enables us to control the extrapolation to the physical light-quark masses and continuum. For the b quarks we use the anisotropic clover action with the relativistic heavy-quark interpretation, such that discretization errors from the heavy-quark action are of the same size as from the light-quark sector. We renormalize the

  13. AVALIAÇÃO DOS TEORES DE Pb, Cd, Sn, Co, Hg, Mo E As EM SOLOS DA PENÍNSULA FILDES - ANTÁRTICA

    Directory of Open Access Journals (Sweden)

    Bruna M. Dalfior

    Full Text Available Antarctic Continent is one of the few places that has not been explored at all, but studies show that this place is suffering interference by human activities. Therefore, monitoring of this region becomes very important. After optimization and verification of the methodology, the concentrations of Pb, Cd, Sn, Co, Hg, Mo and As in soil samples collected in the Fildes Peninsula, King George Island, Antarctica, were determined by ICP-MS. The ranges found (µg kg-1 were: for Pb 525.2-2314.1, for Cd 54.8-193.8, for Sn 54.8-193.8, for Co 2095.0-11094.1, for Hg < 2.4-54.6, for Mo 5.3-38.7 and for As 120.3-1297.1. In general, the presence of these elements can be attributed to different factors, such as natural composition of soil, melting process and transport of chemical elements caused by physical phenomena as sea and air currents, besides anthropic contamination. Using enrichment factor was possible suggest contribution by anthropic activities mainly for Co and As. Thus, it is important monitoring the elements levels constantly assisting in environmental protection.

  14. Mn(II removal from aqueous solutions by Co/Mo layered double hydroxide: Kinetics and thermodynamics

    Directory of Open Access Journals (Sweden)

    A.A. Bakr

    2016-06-01

    Full Text Available This paper deals with the experimental investigation related to the Mn(II removal from aqueous solutions by the adsorption onto a synthesized Co/Mo layered double hydroxide (Co/Mo-LDH. The adsorption behavior was studied as a function of initial Mn(II concentration (40–145 mg/L, contact time (15–90 min, solution pH (2–9 and adsorbent mass (0.05–0.35 g per 1.0 L. All adsorption processes were rapidly carried out at different temperatures (298, 308 and 318 K and constant stirring rate 160 rpm. The results showed that the Co/Mo-LDH is a very promising material for removing of Mn(II from the aqueous solutions. Particularly, the solution pH range of 4–7 has the most significant effect on the adsorption capacity. The results revealed that the maximum adsorption capacities were 20.2, 26.75 and 38.1 mg/g from the initial Mn(II concentration (145 mg/L at pH 5, adsorbent mass (0.2 g/1.0 L, and contact time (60 min at different temperatures, 298, 308 and 318 K, respectively. The adsorption kinetics data are well fitted by the pseudo-second-order model, while the adsorption isotherms data were better fitted by the Langmuir equation. Also, this paper discusses the thermodynamic parameters of the adsorption and the results demonstrate that the adsorption process is spontaneous and endothermic.

  15. Design Strategies for CeO2-MoO3 Catalysts for DeNOx and Hg(0) Oxidation in the Presence of HCl: The Significance of the Surface Acid-Base Properties.

    Science.gov (United States)

    Chang, Huazhen; Wu, Qingru; Zhang, Tao; Li, Mingguan; Sun, Xiaoxu; Li, Junhua; Duan, Lei; Hao, Jiming

    2015-10-20

    A series of CeMoOx catalysts with different surface Ce/Mo ratios was synthesized by a coprecipitation method via changing precipitation pH value. The surface basicity on selective catalytic reduction (SCR) catalysts (CeMoOx and VMo/Ti) was characterized and correlated to the durability and activity of catalyst for simultaneous elimination of NOx and Hg(0). The pH value in the preparation process affected the surface concentrations of Ce and Mo, the Brunauer-Emmett-Teller (BET) specific surface area, and the acid-base properties over the CeMoOx catalysts. The O 1s X-ray photoelectron spectroscopy (XPS) spectra and CO2-temperature programmed desorption (TPD) suggested that the surface basicity increased as the pH value increased. The existence of strong basic sites contributed to the deactivation effect of HCl over the VMo/Ti and CeMoOx catalysts prepared at pH = 12. For the CeMoOx catalysts prepared at pH = 9 and 6, the appearance of surface molybdena species replaced the surface -OH, and the existence of appropriate medium-strength basic sites contributed to their resistance to HCl poisoning in the SCR reaction. Moreover, these sites facilitated the adsorption and activation of HCl and enhanced Hg(0) oxidation. On the other hand, the inhibitory effect of NH3 on Hg(0) oxidation was correlated with the competitive adsorption of NH3 and Hg(0) on acidic surface sites. Therefore, acidic surface sites may play an important role in Hg(0) adsorption. The characterization and balance of basicity and acidity of an SCR catalyst is believed to be helpful in preventing deactivation by acid gas in the SCR reaction and simultaneous Hg(0) oxidation.

  16. Mn2- x Y x (MoO4)3 Phosphor Excited by UV GaN-Based Light-Emitting Diode for White Emission

    Science.gov (United States)

    Chen, Lung-Chien; Tseng, Zong-Liang; Hsu, Ting-Chun; Yang, Shengyi; Chen, Yuan-Bin

    2017-04-01

    One option for low-cost white light-emitting diodes (LEDs) is the combination of a near-ultraviolet (UV) LED chip (382 nm) and a single phosphor. Such Mn2- x Y x (MoO4)3 single phosphors have been fabricated by a simple solid-state reaction route and their emission color tuned by controlling the Mn doping amount. The chromaticity coordinates of the white light emitted by the UV GaN LED with the MnY(MoO4)3 phosphor were x = 0.5204 and y = 0.4050 [correlated color temperature (CCT) = 7958 K].

  17. Synthèse et structure cristalline d'un matériau noir AgMnII3(MnIII0,26Al0,74(MoO45

    Directory of Open Access Journals (Sweden)

    Chahira Bouzidi

    2015-03-01

    Full Text Available A new silver aluminium trimanganese pentamolybdate {silver(I trimanganese(II aluminium pentakis[tetraoxidomolybdate(VI]}, AgMnII3(MnIII0,26Al0,74(MoO45, has been synthesized using solid-state methods. The structure is composed of M2O10 dimers, M3O14 (M = Mn, Al trimers and MoO4 tetrahedra sharing corners and forming three types of layers A, B and B′. The sequence of the constituting layers is A–BB′–A–BB′, with B′ obtained from B by inversion symmetry, forming a three-dimensional structure with large channels in which the positionally disordered and partially occupied Ag+ ions reside. The MnIII and AlIII atoms share the same site, M. AgMnII3(MnIII0,26Al0,74(MoO45 is isotypic with the NaMg3X(MoO45 (X = Al, In family and with NaFe4(MoO45. A comparative structural description is provided between the structure of the title compound and those of related phases containing dimers, trimers and tetramers.

  18. Synthèse et structure cristalline d'un matériau noir AgMn(II) 3(Mn(III) 0,26Al0,74)(MoO4)5.

    Science.gov (United States)

    Bouzidi, Chahira; Frigui, Wafa; Zid, Mohamed Faouzi

    2015-03-01

    A new silver aluminium trimangan-ese penta-molybdate {silver(I) trimanganese(II) aluminium penta-kis-[tetra-oxidomolybdate(VI)]}, AgMn(II) 3(Mn(III) 0,26Al0,74)(MoO4)5, has been synthesized using solid-state methods. The structure is composed of M 2O10 dimers, M 3O14 (M = Mn, Al) trimers and MoO4 tetra-hedra sharing corners and forming three types of layers A, B and B'. The sequence of the constituting layers is A-BB'-A-BB', with B' obtained from B by inversion symmetry, forming a three-dimensional structure with large channels in which the positionally disordered and partially occupied Ag(+) ions reside. The Mn(III) and Al(III) atoms share the same site, M. AgMn(II) 3(Mn(III) 0,26Al0,74)(MoO4)5 is isotypic with the NaMg3 X(MoO4)5 (X = Al, In) family and with NaFe4(MoO4)5. A comparative structural description is provided between the structure of the title compound and those of related phases containing dimers, trimers and tetra-mers.

  19. Magnetotransport properties of Mo substituted La0.7Ca0.3Mn1-xMoxO3 perovskites

    Science.gov (United States)

    Chen, Jenq-Wei; Rao, G. Narsinga

    2016-03-01

    We studied the effects of Mo substitution on the structural, transport, and magnetic properties of the La0.7Ca0.3Mn1-xMoxO3 (x ≤ 0.1) samples. Powder X-ray diffraction analysis reveals that the samples studied crystallize in the orthorhombic structure with space group Pbnm. Both particle size and morphology change significantly as the Mo content x varies. The metal-insulator transition temperature (TMI) and Curie temperature (TC) decrease monotonically as x increases. Magnetization data reveal that long-range FM ordering persists in all samples and the saturation moment decreases linearly as x increases. The smaller depression rate of dTC/dx observed is mainly ascribed to the increased amount of Mn2+ ions with Mo doping, which opens the FM coupling between Mn2+-O-Mn3+ in the samples.

  20. The Effect of Magnetic Field on Resistivity of Hg0.89Mn0.11Te in Different Temperature Range

    Institute of Scientific and Technical Information of China (English)

    WANG Zewen; JIE Wanqi

    2015-01-01

    The resistivity of Hg0.89Mn0.11Te has been measured by the superconducting quantum interference device magnetometer in the temperature range from 5 to 200 K under the applied magnetic ifeld of 1, 2, 4 and 6.5 Tesla, respectively, compared with that of no-magnetic ifeld. The results show that the resistivity increases with increase applied magnetic ifeld at higher temperature from 80 to 200 K, but decreases at lower temperature from 5 to 25 K. There exists a transitive range from 25 to 80 K, where the variation of the resistivity shows different tendencies depending on the strength of magnetic field. Maximum difference of resistivity under 6.5 Tesla from that without magnetic ifeld in the temperature range from 30 to 200 K is only about 5 Ω·cm, but it increases up to 3 orders of magnitude at 5 K. The analysis shows that the variation of resistivity of Hg0.89Mn0.11Te under the magnetic ifeld is the algebraic sum of the transverse direction magnetoresistance effect and the sp-d exchange interaction effect. TDRME plays major role in the high temperature range. However, with the decrease of temperature, the effect ofsp-d EI on the resistivity gradually exceeds that of the transverse direction magnetoresistance effect through the transitive range, and becomes the dominant effect in the temperature range from 5 to 25 K, which leads to the dramatic decrease of resistivity.

  1. Analysis of whole human blood for Pb, Cd, Hg, Se, and Mn by ICP-DRC-MS for biomonitoring and acute exposures.

    Science.gov (United States)

    Jones, Deanna R; Jarrett, Jeffery M; Tevis, Denise S; Franklin, Melanie; Mullinix, Neva J; Wallon, Kristen L; Derrick Quarles, C; Caldwell, Kathleen L; Jones, Robert L

    2017-01-01

    We improved our inductively coupled plasma mass spectrometry (ICP-MS) whole blood method [1] for determination of lead (Pb), cadmium (Cd), and mercury (Hg) by including manganese (Mn) and selenium (Se), and expanding the calibration range of all analytes. The method is validated on a PerkinElmer (PE) ELAN® DRC II ICP-MS (ICP-DRC-MS) and uses the Dynamic Reaction Cell (DRC) technology to attenuate interfering background ion signals via ion-molecule reactions. Methane gas (CH4) eliminates background signal from (40)Ar2(+) to permit determination of (80)Se(+), and oxygen gas (O2) eliminates several polyatomic interferences (e.g. (40)Ar(15)N(+), (54)Fe(1)H(+)) on (55)Mn(+). Hg sensitivity in DRC mode is a factor of two higher than vented mode when measured under the same DRC conditions as Mn due to collisional focusing of the ion beam. To compensate for the expanded method's longer analysis time (due to DRC mode pause delays), we implemented an SC4-FAST autosampler (ESI Scientific, Omaha, NE), which vacuum loads the sample onto a loop, to keep the sample-to-sample measurement time to less than 5min, allowing for preparation and analysis of 60 samples in an 8-h work shift. The longer analysis time also resulted in faster breakdown of the hydrocarbon oil in the interface roughing pump. The replacement of the standard roughing pump with a pump using a fluorinated lubricant, Fomblin®, extended the time between pump maintenance. We optimized the diluent and rinse solution components to reduce carryover from high concentration samples and prevent the formation of precipitates. We performed a robust calculation to determine the following limits of detection (LOD) in whole blood: 0.07µgdL(-1) for Pb, 0.10µgL(-1) for Cd, 0.28μgL(-1) for Hg, 0.99µgL(-1) for Mn, and 24.5µgL(-1) for Se.

  2. A search for pulsations in the HgMn star HD 45975 with CoRoT photometry and ground-based spectroscopy

    Science.gov (United States)

    Morel, T.; Briquet, M.; Auvergne, M.; Alecian, G.; Ghazaryan, S.; Niemczura, E.; Fossati, L.; Lehmann, H.; Hubrig, S.; Ulusoy, C.; Damerdji, Y.; Rainer, M.; Poretti, E.; Borsa, F.; Scardia, M.; Schmid, V. S.; Van Winckel, H.; De Smedt, K.; Pápics, P. I.; Gameiro, J. F.; Waelkens, C.; Fagas, M.; Kamiński, K.; Dimitrov, W.; Baglin, A.; Michel, E.; Dumortier, L.; Frémat, Y.; Hensberge, H.; Jorissen, A.; Van Eck, S.

    2014-01-01

    The existence of pulsations in HgMn stars is still being debated. To provide the first unambiguous observational detection of pulsations in this class of chemically peculiar objects, the bright star HD 45975 was monitored for nearly two months by the CoRoT satellite. Independent analyses of the light curve provide evidence of monoperiodic variations with a frequency of 0.7572 d-1 and a peak-to-peak amplitude of ~2800 ppm. Multisite, ground-based spectroscopic observations overlapping the CoRoT observations show the star to be a long-period, single-lined binary. Furthermore, with the notable exception of mercury, they reveal the same periodicity as in photometry in the line moments of chemical species exhibiting strong overabundances (e.g., Mn and Y). In contrast, lines of other elements do not show significant variations. As found in otherHgMn stars, the pattern of variability consists in an absorption bump moving redwards across the line profiles. We argue that the photometric and spectroscopic changes are more consistent with an interpretation in terms of rotational modulation of spots at the stellar surface. In this framework, the existence of pulsations producing photometric variations above the ~50 ppm level is unlikely in HD 45975. This provides strong constraints on the excitation/damping of pulsation modes in this HgMn star. The CoRoT space mission was developed and is operated by the French space agency CNES, with participation of ESA's RSSD and Science Programmes, Austria, Belgium, Brazil, Germany, and Spain. This work is based on observations collected at La Silla and Paranal Observatories, ESO (Chile), with the HARPS and UVES spectrographs at the 3.6-m and very large telescopes, under programmes LP185.D-0056 and 287.D-5066. It is also based on observations made with the Mercator Telescope, operated on the island of La Palma by the Flemish Community, at the Spanish Observatorio del Roque de los Muchachos of the Instituto de Astrofísica de Canarias

  3. Study on Catalytic Combustion of VOCs over LaMO3 (M = Co, Mn) Perovskite Catalysts%LaMO3(M=Co,Mn)钙钛矿型催化剂上VOCs催化燃烧的研究

    Institute of Scientific and Technical Information of China (English)

    黄海凤; 唐伟; 陈银飞; 陈碧芬

    2004-01-01

    研究了LaMO3(M=Co,Mn)钙钛矿型催化剂对VOCs的催化燃烧性能,该类催化剂对单一VOC和混合VOCs均有很好的催化活性,而LaMnO3的催化活性要比LaCoO3的催化活性更好,氧化还原滴定实验表明,LaMnO3催化剂中锰以Mn4+(大约35%)和Mn3+价态存在,而在LaCoO3催化剂中发现钴均以Co3+价态存在;在混合VOCs催化燃烧的试验中,3种有机物的易氧化性依次为正丙醇>甲苯>环己烷,达到99%的转化率时,环己烷的反应温度则比甲苯的反应温度要约低40℃.

  4. Study of the analytic quality in the determinations of Cr, Fe, Mn, Cu, Zn, Pb and Hg through conventional and nuclear analytical techniques in mosses of the MATV; Estudio de la calidad analitica en las determinaciones de Cr, Fe, Mn, Cu, Zn, Pb y Hg a traves de tecnicas analiticas nucleares y convencionales en musgos de la ZMVT

    Energy Technology Data Exchange (ETDEWEB)

    Caballero S, B.

    2013-07-01

    To evaluate the environmental risks of air pollution and to facilitate the decision-making for control, is necessary to have the capacity to generate data with analytical quality. A comparison between nuclear (Neutron activation analysis and total reflection X-ray fluorescence spectrometry) and no nuclear analytical techniques (atomic absorption spectrometry and inductively coupled plasma optical emission spectrometry) for simultaneous determination of metal content (Cr, Cu, Fe, Hg, Mn, Pb and Zn) in mosses from Metropolitan Area of the Toluca Valley (MATV) was performed. Epiphytic mosses (Fabriona ciliaris and Leskea angustata) were sampled in two campaigns, 16 sites (urban, transition and natural) and were prepared for each technique. The biological certified reference materials were used for the quality control and to evaluate accuracy, precision, linearity, detection and quantification limits. Results show that nuclear analytical techniques and no nuclear applied in chemical analysis of Cr, Cu, Fe, Hg, Mn, Pb and Zn in moss from MATV are comparable and therefore all of these can potentially be used for this purpose. However, if its considered both, the performance parameters and economic/operational characteristics is widely recommended inductively coupled plasma optical emission spectrometry, conventional analytical technique, which showed the highest analytical grade quality. Also were observed spatial and temporal variations in the concentrations of Cr, Cu, Fe, Hg, Mn, Pb and Zn in mosses from MATV and was discussed its potential origin. The urban sites had the highest concentration of anthropogenic elements as Cr, Cu, Fe, Hg, Pb and Zn because are strongly impacted by roads with high vehicle traffic. (Author)

  5. Structural and surface analysis of unsupported and alumina-supported La(Mn,Fe,Mo)O{sub 3} perovskite oxides

    Energy Technology Data Exchange (ETDEWEB)

    Rosmaninho, M.G.; Tristao, J.C.; Moura, F.C.C.; Lago, R.M.; Araujo, M.H. [Universidade Federal de Minas Gerais (UFMG), Departamento de Quimica, ICEx, Minas Gerais (Brazil); Fierro, J.L.G. [Instituto de Catalisis y Petroleoquimica (ICP), Madrid (Spain)

    2010-04-15

    A series of bulk and Al{sub 2}O{sub 3}-supported perovskite oxides of the type LaMn{sub 1-x-y} Fe{sub x} Mo{sub y} O{sub 3} (x=0.00-0.90 and y=0.00-0.09) were synthesized by the citric acid complexation-gelation method followed by annealing in air at 800 C. For all samples, the local environment and the chemical state and concentration of surface species were determined. Moessbauer spectra revealed the only presence of octahedral Fe {sup 3+} ions dispersed in the perovskite structure, however well-crystallized together with a poorly crystalline LaFeO{sub 3} phases were detected for larger substitutions (x=0.90). A similar picture was obtained for Mo-loaded (y=0.02 and 0.05) samples but a new phase most likely related to Fe {sup 3+} ions dispersed aside from the perovskite structure was found for larger substitutions (y=0.09). Together with these structures, supported samples showed the presence of LaFeO{sub 3} nanoparticles. Finally, photoelectron spectroscopy indicated that the chemical state and composition of the samples in the surface region (2-3 nm) approaches that of the bulk. For the unsupported substituted samples, iron (and molybdenum) enters into the perovskite structure while manganese tends to be slightly segregated. Moreover, in supported perovskites, a fraction of Mo and La atoms interact with the alumina surface. All these oxides were active in methane combustion and best performance was recorded for the Fe-rich composition (x=0.9) in which both Mn {sup 3+} and Mo {sup 3+} ions were in the same proportion (y=0.05). (orig.)

  6. Study on the resistance spot welding technology of 22MnMoB hot stamping quenched steel

    Institute of Scientific and Technical Information of China (English)

    Feng Yi; Ma Mingtu; Hua Fuan; Zhang Junping; Song Leifeng; Jin Qingsheng

    2014-01-01

    In this paper,the spot welding technology of a new kind of 22MnMoB hot stamping quenched steel sheet was systematically studied by power frequency spot welder. Through a series of technology and test exper-iments,we have obtained the optimal spot welding technological parameter condition. According to the results, the relations among spot welding technological parameter,welding nugget,mechanical property and fracture mode were discussed. The effects of all the welding parameters such as welding current,welding time and elec-trode force on the quality of joint can be boiled down to one thing-the diameter of welding nugget. The experi-mental results showed that welding nugget diameter determines the mechanical property of spot welding joint and the relation between welding nugget diameter and the mechanical property of joint presents a kind of linear mathematic representation. There are two typical fracture models of 22MnMoB hot stamping quenched steel sheet,i.e.,interfacial fracture and nugget pullout. Other than mild steel or normal high strength steel,in the shearing tensile test,hot stamping quenched steel has a great tendency to fail in interfacial mode due to the ef-fects of high strength matrix structure,welding soft zone and the porosity level of fusion zone.

  7. Combining sedimentological, trace metal (Mn, Mo) and molecular evidence for reconstructing past water-column redox conditions: The example of meromictic Lake Cadagno (Swiss Alps)

    DEFF Research Database (Denmark)

    Wirth, S. B.; Gilli, A.; Niemann, H.

    2013-01-01

    was investigated for concentration variations of the trace metals Mn and Mo (XRF core scanning and ICP-MS measurements), and for the presence of anoxygenic phototrophic sulfur bacteria (carotenoid pigment analysis and 16S rDNA real time PCR). Our trace metal analysis documents an oxic-intermediate-sulfidic redox...... in the sediments (up to 490 ppm), accompanied by an abrupt drop in Mn concentrations and the increase of molecular biomarkers that indicate the presence of anoxygenic photosynthetic bacteria in the water column. Persistently high Mo concentrations >80 ppm provide evidence that sulfidic conditions prevailed...

  8. The Origin of Capacity Fade in the Li2MnO3·LiMO2 (M = Li, Ni, Co, Mn) Microsphere Positive Electrode: An Operando Neutron Diffraction and Transmission X-ray Microscopy Study.

    Science.gov (United States)

    Chen, Chih-Jung; Pang, Wei Kong; Mori, Tatsuhiro; Peterson, Vanessa K; Sharma, Neeraj; Lee, Po-Han; Wu, She-Huang; Wang, Chun-Chieh; Song, Yen-Fang; Liu, Ru-Shi

    2016-07-20

    The mechanism of capacity fade of the Li2MnO3·LiMO2 (M = Li, Ni, Co, Mn) composite positive electrode within a full cell was investigated using a combination of operando neutron powder diffraction and transmission X-ray microscopy methods, enabling the phase, crystallographic, and morphological evolution of the material during electrochemical cycling to be understood. The electrode was shown to initially consist of 73(1) wt % R3̅m LiMO2 with the remaining 27(1) wt % C2/m Li2MnO3 likely existing as an intergrowth. Cracking in the Li2MnO3·LiMO2 electrode particle under operando microscopy observation was revealed to be initiated by the solid-solution reaction of the LiMO2 phase on charge to 4.55 V vs Li(+)/Li and intensified during further charge to 4.7 V vs Li(+)/Li during the concurrent two-phase reaction of the LiMO2 phase, involving the largest lattice change of any phase, and oxygen evolution from the Li2MnO3 phase. Notably, significant healing of the generated cracks in the Li2MnO3·LiMO2 electrode particle occurred during subsequent lithiation on discharge, with this rehealing being principally associated with the solid-solution reaction of the LiMO2 phase. This work reveals that while it is the reduction of lattice size of electrode phases during charge that results in cracking of the Li2MnO3·LiMO2 electrode particle, with the extent of cracking correlated to the magnitude of the size change, crack healing is possible in the reverse solid-solution reaction occurring during discharge. Importantly, it is the phase separation during the two-phase reaction of the LiMO2 phase that prevents the complete healing of the electrode particle, leading to pulverization over extended cycling. This work points to the minimization of behavior leading to phase separation, such as two-phase and oxygen evolution, as a key strategy in preventing capacity fade of the electrode.

  9. Phase transitions and magnetic structures in MnW1-x Mo x O4 compounds (x  ⩽  0.2).

    Science.gov (United States)

    Hardy, Vincent; Payen, Christophe; Damay, Françoise; Meddar, Lynda; Josse, Michaël; Andre, Gilles

    2016-08-24

    Temperature-dependent specific heat, magnetization and neutron diffraction data have been collected in zero magnetic field for polycrystalline samples of MnW1-x Mo x O4 (x  ⩽  0.2) solid solution whose end-member MnWO4 exhibits a magnetoelectric multiferroic phase (AF2 phase) between T 1  ≈  8 K and T 2  =  12.5 K. In MnW1-x Mo x O4, diamagnetic W(6+) are replaced with diamagnetic Mo(6+) cations and magnetic couplings among Mn(2+) (3d (5), S  =  5/2) ions are modified due the doping-induced tuning of the orbital hybridization between Mn 3d and O 2p states. It was observed that magnetic phase transition temperatures which are associated with the second-order AF3-to-paramagnetic (T N) and AF2-to-AF3 (T 2) transitions in pure MnWO4 slightly increase with the Mo content x. Magnetic specific heat data also indicate that the first-order AF1-to-AF2 phase transition at T 1 survives a weak doping x  ⩽  0.05. This latter phase transition becomes invisible above the base temperature 2 K for higher level of doping x  ⩾  0.10. Neutron powder diffraction datasets collected above 1.5 K for a sample of MnW0.8Mo0.2O4 were analyzed using the Rietveld method. The magnetic structure below  ≈  14 K is a helical incommensurate spin order with a temperature-independent propagation vector k  =  (-0.217(6), 0.5, 0.466(4)). This cycloidal magnetic structure is similar to the polar AF2 structure observed in MnWO4. The AF1 up-up-down-down collinear spin arrangement observed in MnWO4 is absent in our MnW0.8Mo0.2O4 sample.

  10. Phase transitions and magnetic structures in MnW1-x Mo x O4 compounds (x  ⩽  0.2)

    Science.gov (United States)

    Hardy, Vincent; Payen, Christophe; Damay, Françoise; Meddar, Lynda; Josse, Michaël; Andre, Gilles

    2016-08-01

    Temperature-dependent specific heat, magnetization and neutron diffraction data have been collected in zero magnetic field for polycrystalline samples of MnW1-x Mo x O4 (x  ⩽  0.2) solid solution whose end-member MnWO4 exhibits a magnetoelectric multiferroic phase (AF2 phase) between T 1  ≈  8 K and T 2  =  12.5 K. In MnW1-x Mo x O4, diamagnetic W6+ are replaced with diamagnetic Mo6+ cations and magnetic couplings among Mn2+ (3d 5, S  =  5/2) ions are modified due the doping-induced tuning of the orbital hybridization between Mn 3d and O 2p states. It was observed that magnetic phase transition temperatures which are associated with the second-order AF3-to-paramagnetic (T N) and AF2-to-AF3 (T 2) transitions in pure MnWO4 slightly increase with the Mo content x. Magnetic specific heat data also indicate that the first-order AF1-to-AF2 phase transition at T 1 survives a weak doping x  ⩽  0.05. This latter phase transition becomes invisible above the base temperature 2 K for higher level of doping x  ⩾  0.10. Neutron powder diffraction datasets collected above 1.5 K for a sample of MnW0.8Mo0.2O4 were analyzed using the Rietveld method. The magnetic structure below  ≈  14 K is a helical incommensurate spin order with a temperature-independent propagation vector k  =  (-0.217(6), 0.5, 0.466(4)). This cycloidal magnetic structure is similar to the polar AF2 structure observed in MnWO4. The AF1 up-up-down-down collinear spin arrangement observed in MnWO4 is absent in our MnW0.8Mo0.2O4 sample.

  11. Microstructure and mechanical properties of railway wheels manufactured with low-medium carbon Si-Mn-Mo-V steel

    Institute of Scientific and Technical Information of China (English)

    Mingru Zhang; Haicheng Gu

    2008-01-01

    The suitability of carbide-free bainite steel as railway wheel materials was investigated. The low-medium carbon Si-Mn-Mo-V steel was designed to make railway wheels by forging and rolling. The slack quenching with water was conducted on the tread of rim section by programmed control to simulate isothermal heat treatment after being austenitized. Microstructures and mechanical properties have been studied. The results indicate that the microstructure of the rim is mainly carbide-free bainite, and the mixed mi- crostructure of bainitic ferrite and granular bainite is observed in web and hub. The mechanical properties are superior to both the standard requirements and the commercial production, such as CL60 plain carbon. The Charpy impact energy is relatively high at room and/or subzero temperatures. The force-displacement curves and fractographies reveal the excellent ability of resistance to crack initiation and propagation.

  12. Characterization of Tensile Strain Hardening Behaviors for 32Mn-7Cr-1Mo-0.3N Cryogenic Austenitic Steel

    Institute of Scientific and Technical Information of China (English)

    Liang QIU; Ruidong FU; Cunyu WANG; Yangzeng ZHENG

    2006-01-01

    The strain hardening behaviors of 32Mn-7Cr-1Mo-0.3N austenitic steel were characterized by a simple and effective method. The results show that Hollomon relationship is not applicable during total uniform deformation stage. The flow equation was proposed, Inσ=aexp(lnε/b)+c. The variation rates of strain hardening exponents with true strain at 77 K are obviously higher than that at other temperatures and the value of d2σ/dε2 becomes positive during high strain stage. The characters of this variation are principal reasons for increasing elongation at 77 K. The forming of mechanical twin as well as ε-martensite leads to a high elongation at 77 K.

  13. Analysis of fracture toughness in transition temperature region of a Mn-Mo-Ni low-alloy steel

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Sang Ho; Hwang, Byoung Chul; Lee, Sung Hak [Pohang Univ. of Science and Technology, Pohang (Korea, Republic of)

    2002-08-01

    This study is concerned with the analysis of fracture toughness in the transition region of a Mn-Mo-Ni low-alloy steel according to ASTM E1921 standard test method. Elastic-plastic cleavage fracture toughness, K{sub Jc} was determined by 3-point bend tests, using precracked Charpy V-notch (PCVN) specimens, and then the measured K{sub Jc} values were interpreted by the 3-parameter Weibull distribution with a theoretical slope of 4. fractographic observation indicated that the critical distance from a precrack tip to a cleavage initiation site linearly increased with increasing the critical J(J{sub c}) value, and that the stretch zone width had a good correlation with K{sub Jc} value, irrespective of testing temperature. Relationship between J{sub c} and critical distance, local fracture stress, and plane strain fracture toughness were discussed on the basis of the cleavage fracture behavior in the transition temperature region.

  14. Nickel and Copper-Free Sintered Structural Steels Containing Mn, Cr, Si, and Mo Developed for High Performance Applications

    Directory of Open Access Journals (Sweden)

    Cias A.

    2017-03-01

    Full Text Available In an attempt to study the sinterability of potential high-strength nickel-free sintered structural steels containing Mn, Cr, Si and Mo compacts were prepared based on sponge and water atomised iron powders and on Astaloy prealloyed powders. To these were admixed ferromanganese, ferroslicon, and graphite. The samples were sintered at temperatures 1120 and 1250°C in laboratory tube furnaces in hydrogen, hydrogen-nitrogen atmospheres with dew points better than -60°C or in nitrogen in a semiclosed container in a local microatmosphere. After sintering the samples were slowly cooled or sinterhardened. Generally resultant microstructures were inhomogeneous, consisted of pearlite/ bainite/martensite, but were characterised by an absence of oxide networks. Sintering studies performed over a range of compositions have shown that superior strength, ranging beyond 900 MPa, along with reasonable tensile elongation, can be achieved with these new steels.

  15. HEAVY METALS (Hg, Cu, Mn, Cr e Ni CONTENTS IN THE RIO DAS PEDRAS LAGOON, MOJI-GUAÇU RIVER BASIN (SÃO PAULO STATE, BRAZIL = HISTÓRICO DA PRESENÇA DE METAIS PESADOS (Hg, Cu, Mn, Cr e Ni NA LAGOA RIO DAS PEDRAS, BACIA DO RIO MOJI-GUAÇU -SP, BRASIL

    Directory of Open Access Journals (Sweden)

    Claudinéia Raquel de Oliveira

    2003-01-01

    Full Text Available The presence of heavy metals in a sediment profile from the Rio das Pedras lagoon, located at the Moji-Guaçu river floodplain, São Paulo, was investigated. Samples were stratified at each 1 cm, sieved in 63 m m and digested in a strong acid solution (HNO3 + HF + HClO4 in PTFE bomb. The extracts were analyzed by emission plasma spectrometry (ICP-AES for Al, Cu, Mn, Cr and Ni contents. For Hg, the direct pyrolysis of samples and atomic fluorescence spectrometry detector AFS were employed. By using Al as a normalizer agent, an enrichment of metals concentration, with exception for Mn was observed. Average concentration for Cu (0.12 mg g-1 and Mn (1.12 mg g-1 were considered high in comparison to those concentrations in an unpolluted environment. Probably, these data are related to the agricultural activity (sugarcane plantation around the lagoon, or to the Moji-Guaçu river transport in the flood season. Hg, Cr and Niconcentrations were similar the those verified in unpolluted areas. The chronology inventigation, determined by the 210Pb technique, indicated that the 25 cm long sediment profile shows a 135 years of deposition history of the suspended material in this lagoon. = A presença de metais pesados em perfil de sedimento coletado na Lagoa Rio das Pedras, localizada na planície de inundação do rio Moji-Guaçu, São Paulo, foi investigada. Amostras estratificadas a cada 1 cm foram peneiradas a 63 m m e digeridas através de ataque ácido (HNO3 + HF + HClO4 em bombas de PTFE. Os extratos obtidos foram analisados quanto aos teores de Al, Cu, Mn, Cr e Ni por espectrometria de emissão de plasma (ICP-AES. Para Hg, empregou-se a pirólise direta da amostra e detecção por AFS. Utilizando-se Al como elemento normalizador, observou-se enriquecimento nos teores de metais pesados para anos recentes, exceto para Mn. As concentrações médias de Cu (0,12 mg g-1 e Mn (1,12 mg g-1 para amostras de sedimentos foram elevadas, em comparação

  16. LaMn1-xFe xO3 and LaMn0.1-xFe0.90Mo x O3 perovskites: synthesis, characterization and catalytic activity in H2O2 reactions

    Directory of Open Access Journals (Sweden)

    Fabiano Magalhães

    2008-09-01

    Full Text Available In this work two perovskites were prepared: LaMn1-xFe xO3, and LaMn0.1-x Fe0.90Mo xO3. XRD and Mössbauer spectroscopy suggest the formation of pure phase perovskite with the incorporation of Fe and Mo in the structure. The catalytic activity of these materials was studied in two reactions with H2O2: the decomposition to O2, and the oxidation of the model organic contaminant methylene blue. The perovskite composition strongly affects the catalytic activity, while Fe decreases the H2O2 decomposition Mo strongly improves dye oxidation.

  17. Preparation and characterization of phosphate glass system A2MnMP2O10 (A = Li, Na, K and (M = W, Mo

    Directory of Open Access Journals (Sweden)

    Moutataouia M.

    2013-09-01

    Full Text Available New materials based glassy phosphates and transition elements A2MnMP2O10 (A = Li, Na, K and (M = Mo, W were prepared by direct fusion of the mixture of the reactants followed by quenching in the air. Analysis by X-ray diffraction showed that the obtained materials are amorphous. Differential scanning calorimetry DSC was used to determine the glass transition (Tg and crystallization (Tc temperatures. The thermal stability of tungsten glasses is higher than that of molybdenum ones. Tungsten plays, certainly, a role of cross-linking polyphosphate groups by creating more covalent new bonds P-O-W and W-O-W. Moreover, it has been shown that lithium glasses are more stable than sodium and potassium, probably due to the potassium hygroscopy. Raman analysis confirms that the studied glasses have similar structures and the predominant structural units are PO4, P2O7 and MO6 polyhedra (M = W, Mo, Mn.

  18. High coercivity in mechanically milled ThMn12-type Nd-Fe-Mo nitrides

    Science.gov (United States)

    Zhang, Xiao-dong; Cheng, Ben-pei; Yang, Ying-chang

    2000-12-01

    Starting from carefully homogenized Nd10Fe90-yMoy (y=12, 10, 7) alloys and by appropriate mechanical milling, the as-milled microstructure consisting of a nanoscale mixture of severely distorted 1:12 phase and substitutional α-Fe-based solid solution was obtained. This kind of as-milled microstructure was thought to have a critical effect on the formation of iron-free nanocrystalline 1:12 phase during subsequent annealing. Upon nitrogenation, the sample of Nd10Fe78Mo12Nx exhibited a record-high coercivity of 13.1 kOe at 293 K. Measurements of initial magnetization curve and a family of demagnetization curves engendered under different maximum applied fields Hm were carried out, and the results revealed the domain-wall pinning at grain boundaries as the coercivity mechanism. A low Mo-content sample of Nd10Fe83Mo7Nx with iHc˜5.8 kOe, Br˜6.8 kG, and (BH)max˜7.0 MG Oe was made by optimizing the preparation conditions.

  19. Chemical surface inhomogeneities in late B-type stars with Hg and Mn peculiarity I Spot evolution in HD 11753 on short and long time scales

    CERN Document Server

    Korhonen, H; Briquet, M; Soriano, M Flores; Hubrig, S; Savanov, I; Hackman, T; Ilyin, I V; Eulaers, E; Pessemier, W

    2013-01-01

    Aims: Time series of high-resolution spectra of the late B-type star HD 11753 exhibiting HgMn chemical peculiarity are used to study the surface distribution of different chemical elements and their temporal evolution. Methods: High-resolution and high signal-to-noise ratio spectra were obtained using the CORALIE spectrograph at La Silla in 2000, 2009, and 2010. Surface maps of YII, SrII, TiII, and CrII were calculated using the Doppler imaging technique. The results were also compared to equivalent width measurements. The evolution of chemical spots both on short and long time scales were investigated. Results: We determine the binary orbit of HD 11753 and fine-tune the rotation period of the primary. The earlier discovered fast evolution of the chemical spots is confirmed by an analysis using both the chemical spot maps and equivalent width measurements. In addition, a long-term decrease in the overall YII and SrII abundances is discovered. A detailed analysis of the chemical spot configurations reveals som...

  20. Abundancias químicas de las estrellas CP del grupo HgMn μ Leporis y 53 Tauri. II. Boro, Berilio, Carbono, Magnesio, Aluminio y Silicio

    Science.gov (United States)

    López García, Z.; Malaroda, S. M.; Faraggiana, R.

    Se determinan las abundancias químicas de los elementos más livianos presentes en dos estrellas CP del grupo HgMn, μ Lep y 53 Tau, utilizando espectros IUE de alta resolución y técnicas de cálculo de espectros sintéticos. Para el cálculo de las líneas se utiliza la lista mas completa de datos atómicos disponible y el programa SYNTHE. Para el cálculo de la abundancia de un elemento se comparan, para cada imagen, los perfiles observados del mayor número de líneas presentes con los perfiles calculados obtenidos por variación de las abundancias iniciales, reteniendo la abundancia para la cual el acuerdo entre las líneas observadas y calculadas es considerado visualmente el mejor. Los resultados obtenidos son comparados con los estimados por la teoría de la difusión.

  1. Distribution and accumulation of elements (As, Cu, Fe, Hg, Mn, and Zn) in tissues of fish species from different trophic levels in the Danube River at the confluence with the Sava River (Serbia).

    Science.gov (United States)

    Subotić, S; Višnjić Jeftić, Ž; Spasić, S; Hegediš, A; Krpo-Ćetković, J; Lenhardt, M

    2013-08-01

    Pikeperch (Sander lucioperca), European catfish (Silurus glanis), common carp (Cyprinus carpio), and gobies (Neogobius gymnotrachelus, Neogobius melanostomus) were collected from the Danube River (Belgrade section), and samples of liver, muscle, or whole-body composites (in the case of gobies) were analyzed for As, Cu, Fe, Hg, Mn, and Zn with inductively coupled plasma optical spectrometry to find out if there was a correlation between accumulation of these elements in predatory and prey species, as well as in pairs of species with overlapping diets. Concentrations of all analyzed elements were either higher (Cu, Fe, Mn, Zn) in liver than in muscle, or equal (As, Hg), except for Hg in carp, which was higher in muscle. Mercury concentration in liver and muscle of predators (catfish, pikeperch) was significantly (<10(-4)) higher than in prey fishes (carp and gobies). The results indicate that Hg concentration was biomagnified through the food chain. Concentrations of As, Fe, and Hg in carp liver and gobies whole-body composite were similar, but carp had significantly (<10(-4)) higher values of Zn and Cu in liver. The regression analysis and trendline equations indicate that the concentrations of all tested elements, except for As in liver, and Mn and Fe in muscle, were similar in predatory fish (pikeperch and catfish), on one hand, and in prey fish (carp and gobies), on the other hand. Distinctly high Zn concentration in carp is very common in this species due to its physiology. Concentrations of Hg and Zn were higher than the maximum acceptable concentration due to the high pollution level in this section of the Danube River, accordingly posing a risk for the human consumption of these fish species.

  2. Changing Rule of Carbon-Enriched Zone and Diffusion Behavior of Carbon in Aging 0Cr6Mn13Ni10MoTi/1Cr5Mo Dissimilar Welded Joints

    Institute of Scientific and Technical Information of China (English)

    Zheng LIU; Ligang WANG; Lai WANG

    2004-01-01

    The microstructures, the changing rule of carbon-enriched zone, the diffusion behaviors of elements C and Cr, and the carbide type of 0Cr6Mn13Ni10MoTi/1Cr5Mo dissimilar welded joints after aging at 500℃ for various times and after long-term service in technical practice were investigated by using the optical microscopy, electron probe microanalysis, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The results show that in aging 0Cr6Mn13Ni10MoTi/1Cr5Mo dissimilar welded joints, the main carbides are M3C and a few carbides are M7C3 and M23C6. The M3C carbide decomposition and dissolution with increasing aging time or aging temperature and the anti-diffusion of C and Cr cause the decrease and disappearance of the carbon-enriched zone. The results are different from those of the A302/1Cr5Mo dissimilar welded joints in previous studies.

  3. Effects of Mn and Cu on the Mechanical Properties of a High Strength Low Alloy NiCrMoV Steel

    Institute of Scientific and Technical Information of China (English)

    A.Abdollah-zadeh; M. Belbasy

    2005-01-01

    The present study focuses on the effects of Mn and Cu on the mechanical properties, in particular, strength and toughness of a low alloy steel containing Ni, Cr, Mo and V. Specimens with different amounts of Mn (0.23%~0.85%)and Cu (0.15%~0.45%) were cast and forged, and then austenitized at 870℃ for 1 h, followed by oil quenching. All specimens were tempered at 650℃ for 1 h. The results show that as the amounts of Mn and Cu increase respectively from 0.35% to 0.85% and from 0.15% to 0.45%, the yield and tensile strength increase. The highest impact energies were observed in the specimen with 0.35% Mn and in the specimen with 0.25% Cu. The impact energy decreases with increasing the Mn and Cu from 0.35% to 0.85% and from 0.25% to 0.45%, respectively. Furthermore, the variation of Mn and Cu does not cause a considerable change in the tempered martensite microstructure. The optimum strength and toughness is observed in 0.35% Mn containing steel and in the 0.25% Cu containing steel.

  4. Chemical reactions during sintering of Fe-Cr-Mn-Si-Ni-Mo-C-steels with special reference to processing in semi-closed containers

    Directory of Open Access Journals (Sweden)

    Cias A.

    2015-01-01

    Full Text Available Sintering of Cr, Mn and Si bearing steels has recently attracted both experimental and theoretical attention and processing in semiclosed containers has been reproposed. This paper brings together relevant thermodynamic data and considers the kinetics of some relevant chemical reactions. These involve iron and carbon, water vapour, carbon monoxide and dioxide, hydrogen and nitrogen of the sintering atmospheres and the alloying elements Cr, Mn, Mo and Si. The paper concludes by presenting mechanical properties data for three steels sintered in local microatmosphere with nitrogen, hydrogen, nitrogen-5% hydrogen and air as the furnace gas.

  5. 139La nuclear magnetic resonance characterisation of La2O3 and La1-xSrxMO3 where M = Cr, Mn or Co.

    Science.gov (United States)

    Bastow, T J

    1994-02-01

    139La Nuclear magnetic resonance (NMR) spectra have been used to obtain nuclear quadrupole coupling parameters for La2O3 and a series of perovskites La1-xSrxMO3 (where M = Cr, Mn or Co). Depending on the doping level of SrO2 these materials are either paramagnetic or ferromagnetic at room temperature. Magnetic transferred hyperfine effects are strongly in evidence in the Mn compounds. A 59Co NMR spectrum was observed in LaCoO3. A precision measurement of the nuclear quadrupole coupling constant in La2O3 was made by nuclear quadrupole resonance (NQR) spectroscopy.

  6. Hg2CuTi型Mn2NiGe合金的电子结构、磁性对压力、四方变形的响应%The responses of electronic structure and magnetism to pressure and tetragonal distortion in the Hg2CuTi-type Mn2NiGe alloy

    Institute of Scientific and Technical Information of China (English)

    罗礼进; 仲崇贵; 方靖淮; 赵永林; 周朋霞; 江学范

    2011-01-01

    By the first-principles method based on the density functional theory, we investigate the responses of electronic structure and magnetism to pressure and tetragonal distortion in the Hg2CuTi-type Mn2NiGe alloy. The results show that: I) With increasing the impressed pressure, the hybridization degree will be enhanced due to the reduction of the Ni-Mn interatomic distance, which leads to the moving to lower energy and the diminishing of the amplitude for the density of states, ii) In the process of transformation from the austenite phase to the martensite phase, the hybridization degree will also be enhanced due to the reduction of the Ni-Mn interatomic distance, the density of states of the occupied state moves to the lower energy and the system energy decreases. Meanwhile, the bonding state moves to the lower energy and the antibonding state moves to the higher energy, the energy band becomes broader and the bonding interaction becomes stronger, which lead to the increasing of the stabilization of martensitic phase, iii) In the process of tetragonal distortions,the change of total magnetic moment ismainly induced by the change of magnetic moment of Ni atom.%运用基于密度泛函理论的第一性原理方法,研究了Hg2 CuTi型Mn2 NiGe合金的电子结构对外加压力的响应以及Mn2 NiGe的电子结构、磁性对四方变形的响应.结果表明:i)随着外加压力的增加,因Ni、Mn原子间距的减小而导致杂化程度的增强,使得态密度整体向低能区域移动,同时,态密度幅度整体略有减小;ii)在由奥氏体相到马氏体相的变形中,同样因Ni、Mn原子间距的减小而导致杂化程度的增强,占据态的态密度向低能区域移动,体系的能量降低,同时,成键态向低能方向移动,反键态向高能方向移动,能带变宽,成键作用加强,最终导致在马氏体相中的稳定性增大;iii)在四方变形过程中,Mn2 NiCe总磁矩的变化主要由Ni原子磁矩的变化所产生.

  7. A magnetic atomic laminate from thin film synthesis: (Mo{sub 0.5}Mn{sub 0.5}){sub 2}GaC

    Energy Technology Data Exchange (ETDEWEB)

    Meshkian, R., E-mail: rahele.meshkian@liu.se; Ingason, A. S.; Lu, J.; Rosen, J. [Department of Physics, Chemistry, and Biology (IFM), Linköping University, SE-581 83 Linköping (Sweden); Arnalds, U. B. [Science Institute, University of Iceland, IS-107 Reykjavik (Iceland); Magnus, F. [Department of Physics and Astronomy, Uppsala University, Box 516, SE-516 Uppsala (Sweden)

    2015-07-01

    We present synthesis and characterization of a new magnetic atomic laminate: (Mo{sub 0.5}Mn{sub 0.5}){sub 2}GaC. High quality crystalline films were synthesized on MgO(111) substrates at a temperature of ∼530 °C. The films display a magnetic response, evaluated by vibrating sample magnetometry, in a temperature range 3-300 K and in a field up to 5 T. The response ranges from ferromagnetic to paramagnetic with change in temperature, with an acquired 5T-moment and remanent moment at 3 K of 0.66 and 0.35 μ{sub B} per metal atom (Mo and Mn), respectively. The remanent moment and the coercive field (0.06 T) exceed all values reported to date for the family of magnetic laminates based on so called MAX phases.

  8. First principle study of the surface reactivity of layered lithium oxides LiMO2 (M = Ni, Mn, Co)

    Science.gov (United States)

    Vallverdu, Germain; Minvielle, Marie; Andreu, Nathalie; Gonbeau, Danielle; Baraille, Isabelle

    2016-07-01

    LiNixMnyCo1 - x - yO2 compounds (NMC) are layered oxides widely used in commercial lithium-ion batteries at the positive electrode. Nevertheless surface reactivity of this material is still not well known. As a first step, based on first principle calculations, this study deals with the electronic properties and the surface reactivity of LiMO2 (M = Co, Ni, Mn) compounds, considering the behavior of each transition metal separately in the same R 3 ̅ mα-NaFeO2-type structure, the one of LiCoO2 and NMC. For each compound, after a brief description of the bare slab electronic properties, we explored the acido-basic and redox properties of the (110) and (104) surfaces by considering the adsorption of a gaseous probe. The chemisorption of SO2 produces both sulfite or sulfate species associated respectively to an acido-basic or a reduction process. These processes are localized on the transition metals of the first two layers of the surface. Although sulfate species are globally favored, a different behavior is obtained depending on both the surface and the transition metal considered. We conclude with a simple scheme which describes the reduction processes on the both surfaces in terms of formal oxidation degrees of transition metals.

  9. Solid Solution Nitriding Technology of 15Cr-7.5Mn-2.6Mo Duplex Stainless Steel

    Institute of Scientific and Technical Information of China (English)

    FU Rui-dong; ZHAO Pin; WANG Chun-Yu; QIU Liang; ZHENG Yang-zeng

    2004-01-01

    Solid solution nitriding technologies of 15Cr-7.5Mn-2.6Mo duplex stainless steel were investigated by using of orthogonal tests. The results show that the best technology would be the processes of 1050℃× 2h + 1150℃× 3h +1050℃× 2h + 1150℃× 4h under pure N2 with PN2=0.15MPa. The high nitrogen austenitic case with the depth of1.62mm can be obtained. Orthogonal tests show that the type of atmosphere has the most notable effect on solid solution nitriding process; the pressure in the furnace and the nitriding processes has a notable effect. X-ray diffraction analyses results indicate that the main phases in the cases of the solution-nitrided samples cooled in the furnace are high nitrogen austenite, CrN, Fe3O4 and nitrogen containing ferrite. In the other samples experienced solid solution nitriding and solution treatment the obtained phase in the cases is high nitrogen austenite only. The results show that solid solution nitriding is a process that nitrogen absolutely diffuses in the austenite. The diffusing activation energy in the conditions of PN2 = 0.15MPa and 1050℃~ 1200℃ is 186.6K J/mol.

  10. Effect of austempering process on microstructure and wear behavior of ductile iron containing Mn-Ni-Cu-Mo

    Science.gov (United States)

    PourAsiabi, HaMiD; Saghafian, Hasan; Pourasiabi, Hamed

    2013-01-01

    In this work, the effects of austempering time and temperature on the microstructure and sliding wear behavior of a Mn-Ni-Cu-Mo alloyed ductile iron were investigated. Ductile iron samples with the desired chemical composition were cast according to ASTM A897M-1990 Y-block. Wear test samples austenitized at 900 °C for 90 min, were austempered at 260, 290 and 320 °C for 30, 60, 90 and 120 min. The wear tests on samples were conducted by Block-on-Ring testing machine according to ASTM G77-98 standard, at the applied load of 75N and the displacement speed of 3.27 m/s. The results showed that the sample austempered at 260 °C for 90 min exhibited the maximum relative wear resistance in comparison with the as-cast sample. The X-ray diffraction patterns of wear debris and the SEM observations of worn surfaces and crosssection of worn surfaces together with wear debris showed that delamination associated with oxidation is the dominant wear mechanism in the samples.

  11. Analysis of fracture toughness in the transition-temperature region of an Mn-Mo-Ni low-alloy steel

    Science.gov (United States)

    Kim, Sangho; Hwang, Byoungchul; Lee, Sunghak; Lee, Sunghak

    2003-06-01

    This study is concerned with the analysis of fracture toughness in the transition region of an Mn-Mo-Ni low-alloy steel, in accordance with the ASTM E1921 standard test method. Elastic-plastic cleavage fracture toughness ( K Jc ) was determined by three-point bend tests, using precracked Charpy V-notch (PCVN) specimens, and relationships between K Jc , the critical component of J ( J c ), critical distance ( X c ), stretch-zone width (SZW), local fracture stress, and plane-strain fracture toughness ( K Ic were discussed on the basis of the cleavage fracture behavior in the transition region. The master curve and the 95 pct confidence curves well explained the variation in the measured K Jc , and the Weibull slope measured on the Weibull plots was consistent with the theoretical slope of 4. Fractographic observation indicated that X c linearly increased with increasing J c , and that the SZW had a good correlation with K Jc , irrespective of the test temperature. In addition, the local fracture stress was independent of the test temperature, because the tempered bainitic steel used in this study showed a propagation-controlled cleavage fracture behavior.

  12. Effects of grain size on fracture toughness in transition temperature region of Mn-Mo-Ni low-alloy steels

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Sangho; Lee, Sunghak; Lee, Bong Sang

    2003-10-25

    An investigation was conducted into the effect of grain size on fracture toughness in the transition temperature region of Mn-Mo-Ni low-alloy steels used for nuclear pressure vessels. Three kinds of steels with different austenite grain sizes (AGS) were fabricated by varying the contents of Al and N, and their microstructures and mechanical properties were examined. Elastic-plastic cleavage fracture toughness, K{sub Jc}, was determined by three-point bend tests of precracked Charpy V-notch (PCVN) specimens according to ASTM E1921 standard test method. When the AGS decreased, the total number of carbides increased, while the size and the aspect ratio of carbides decreased. Local fracture stresses, estimated from a theoretical stress distribution in front of a crack tip, were found to be mainly determined by the 92nd% size of carbides. Cross-sectional areas beneath fracture surfaces were observed to understand microstructural features to affect the cleavage crack propagation behavior. The results showed that measured cleavage fracture units were smaller than AGSs, indicating that packet boundaries as well as austenite grain boundaries played an important role in the cleavage crack propagation. Based on the electron back-scatter diffraction (EBSD) results, the cleavage fracture units could also be matched with the effective grain sizes determined by the misorientation tolerance angle of 25 deg.

  13. Relationship between grain size and fracture toughness in transition region of Mn-Mo-Ni low-alloy steels

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Sang Ho; Lee, Sung Hak [Pohang Univ. of Science and Technology, Pohang (Korea, Republic of); Oh, Yong Jun [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2002-03-01

    The present study aims at interpreting the effect of grain size on fracture toughness in the transition region of Mn-Mo-Ni low-alloy steels. Three kinds of steels with different austenite grain sizes were fabricated, and their microstructures and mechanical properties were examined. Elastic-plastic cleavage fracture toughness, K{sub Jc}, was determined by 3-point bend tests of precracked Charpy V-notch (PCVN) specimens according to ASTM E1921 standard test method. When the austenite grain size decreased, the total number of carbides increased, while the size and the aspect ratio of carbides decreased. Local fracture stresses, estimated from a theoretical stress distribution in front of a crack tip, were found to be mainly determined by the 92%th size of carbides. Cross-sectional areas beneath fracture surfaces were observed to understand microstructural features to affect the cleavage crack propagation behavior. The results showed that measured cleavage fracture units were smaller than austenite grain sizes, indicating that packet boundaries as well as austenite grain boundaries played an important role in the cleavage crack propagation. Based on the electron back-scatter diffraction (EBSD) results, the cleavage fracture units could also be matched with the effective grain sizes determined by the misorientation tolerance angle of 25 degree.

  14. Mo, Mn and La doped TiO{sub 2}: Synthesis, characterization and photocatalytic activity for the decolourization of three different chromophoric dyes

    Energy Technology Data Exchange (ETDEWEB)

    Umar, K.; Haque, M.M. [Department of Chemistry, Aligarh Muslim University, Aligarh 202 002 (India); Muneer, M., E-mail: readermuneer@gmail.com [Department of Chemistry, Aligarh Muslim University, Aligarh 202 002 (India); Harada, T.; Matsumura, M. [Research Center for Solar Energy Chemistry, Osaka University, 1-3 Machikaneyama, Toyonaka 560-8531 (Japan)

    2013-11-25

    Highlights: •Detail study on synthesis, characterization and photocatalytic activity of doped-TiO{sub 2}. •SEM images indicates partial crystalline nature with rough surfaces. •The XRD analysis shows the partial crystalline nature and anatase phase. •The UV–Vis absorption spectra showed λ{sub max} shift towards longer wavelength. •TiO{sub 2} with dopant 0.75% (Mo), 1.0% (Mn, La) showed best photocatalytic efficiency. -- Abstract: Nanocrystalline TiO{sub 2} particles doped with different concentrations of Molybdenum (Mo), Manganese (Mn) and Lanthanum (La) (0.25–1.0%) were synthesized using sol–gel method and characterized by standard analytical techniques such as X-ray diffraction (XRD), UV–Vis spectroscopy and Scanning Electron Microscopy (SEM). The XRD analysis shows the partial crystalline nature and anatase phase. The SEM images of undoped and doped TiO{sub 2} at different magnifications also show the partial crystalline nature with rough surfaces. The photocatalytic activity of the synthesized particles (TiO{sub 2} doped with Mo, Mn and La) was tested by studying the decolourization of three different chromophoric dyes such as Acid Red 88 (azo dye), Gentian Violet (triphenylmethane dye) and Remazol Brilliant Blue R (anthraquinone dye) as a function of time on irradiation in aqueous suspension in an immersion well photochemical reactor with a 500 W halogen linear lamp in the presence of atmospheric oxygen. The results indicate that TiO{sub 2} with dopant concentration of 0.75% (Mo) and 1.0% (Mn, La) showed the highest photocatalytic activity as compared to the other dopant concentrations for the decolourization of all the dyes.

  15. Synthesis and characterization of a novel sodium transition metal oxyfluoride: NaMnMoO3F3·H2O.

    Science.gov (United States)

    Nava-Avendaño, Jessica; Frontera, Carlos; Ayllón, José A; Oró-Solé, Judith; Senguttuvan, Premkumar; Palacín, M Rosa

    2013-09-03

    NaMnMoO3F3·H2O was precipitated at low temperature from aqueous dissolutions of Na2MoO4·2H2O in aqueous HF (or NaHF2) using either Mn(CH3COO)2·4H2O or MnF2 as manganese precursors. Chemical analysis, IR spectra, and effective paramagnetic moment are in agreement with the proposed formula. Electron microscopy studies indicate that the sample is constituted of very thin plate-like microcrystals. The average crystal structure (a = 3.5947(1), b = 21.246(1), and c = 7.3893(2) Å and Cmcm (No. 63) SG) has been elucidated through powder diffraction methods (synchrotron and neutron). Tiny superstructure peaks are observed that can be indexed with the space group Pbca and cell parameters a = 7.1894(2), b = 21.246(1), and c = 7.3893(2) Å. Electron diffraction confirms the doubling of a parameter. Ordering of O and F is proposed in agreement with Pauling's second crystal rule and bond strength sums for each anionic position. The structure that is formed has a layered stacking arrangement along the b-axis of the MnO4F2 octahedra layers that share corners along a- and c-directions. The large interlayer space contains MoO4F2 octahedra (connected to the layer) together with sodium ions and water molecules, tentatively forming hydrogen bonding with fluorine anions. The origin of the superstructure could not be fully elucidated, but it is presumably related to slight distortions within the MnO4F2 octahedra.

  16. Microstructures and electrochemical characteristics of LaNi{sub 3.70}Co{sub 0.2−x}Mn{sub 0.30}Al{sub 0.15}Cu{sub 0.65}(Mo{sub 0.46}Fe{sub 0.54}){sub x} hydrogen storage alloys

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Junling; Fan, Yanping [School of Materials Science & Engineering, Henan Polytechnic University, Jiaozuo 454000 (China); Liu, Baozhong, E-mail: b_z_liu@163.com [School of Materials Science & Engineering, Henan Polytechnic University, Jiaozuo 454000 (China); Ji, Liqiang; Wang, Yongguang [Inner Mongolia Rare Earth Ovonic Metal Hydride Co. Ltd., Baotou 014030 (China); Ma, Mingjie, E-mail: mingjie8@163.com [School of Materials Science & Engineering, Henan Polytechnic University, Jiaozuo 454000 (China)

    2015-08-25

    Highlights: • Commercial Mo{sub 0.46}Fe{sub 0.54} is much cheaper and has lower melting point. • Alloys containing Mo{sub 0.46}Fe{sub 0.54} consist of LaNi{sub 5} phase and Mo phase. • Activation property is improved by increasing Mo{sub 0.46}Fe{sub 0.54} content. • The alloy with x = 0.15 exhibits the best HRD. • C{sub max} and cycling stability decrease with increasing x value. - Abstract: Electrochemical hydrogen storage properties of LaNi{sub 3.70}Co{sub 0.2}Mn{sub 0.30}Al{sub 0.15}Cu{sub 0.65} alloy are improved by substituting Co with Mo{sub 0.46}Fe{sub 0.54}, rather than pure Mo and Fe. Microstructures and electrochemical properties of LaNi{sub 3.70}Co{sub 0.2−x}Mn{sub 0.30}Al{sub 0.15}Cu{sub 0.65}(Mo{sub 0.46}Fe{sub 0.54}){sub x} (x = 0–0.20) hydrogen storage alloys are investigated. X-ray diffraction and backscattered electron results indicate that the pristine alloy is LaNi{sub 5} phase with a hexagonal CaCu{sub 5}-type structure, while the alloys containing Mo{sub 0.46}Fe{sub 0.54} consist of LaNi{sub 5} matrix phase and Mo secondary phase. The relative abundance of Mo phase increases with the increase in x value. The lattice parameters a, c, c/a and cell volume V of LaNi{sub 5} phase increase with increasing x value. As x increases from 0 to 0.20, maximum discharge capacity of the alloy electrodes monotonically decreases from 335.4 (x = 0) to 324.2 mA h/g (x = 0.20). The high-rate dischargeability of the alloy electrodes at the discharge current density of 1200 mA/g first increases from 59.8% (x = 0) to 69.6% (x = 0.15), and then decreases to 64.0% (x = 0.20). The cycling capacity retention rate at the 100th cycle decreases from 80.4% (x = 0) to 61.9% (x = 0.20), which should be ascribed to the deterioration of the corrosion resistance of alloy electrode with increasing x value.

  17. Fermi arc electronic structure and Chern numbers in the type-II Weyl semimetal candidate MoxW<mn>1mn><mo>-mo>xTe<mn>2mn>

    Energy Technology Data Exchange (ETDEWEB)

    Belopolski, Ilya; Xu, Su-Yang; Ishida, Yukiaki; Pan, Xingchen; Yu, Peng; Sanchez, Daniel S.; Zheng, Hao; Neupane, Madhab; Alidoust, Nasser; Chang, Guoqing; Chang, Tay-Rong; Wu, Yun; Bian, Guang; Huang, Shin-Ming; Lee, Chi-Cheng; Mou, Daixiang; Huang, Lunan; Song, You; Wang, Baigeng; Wang, Guanghou; Yeh, Yao-Wen; Yao, Nan; Rault, Julien E.; Le Fèvre, Patrick; Bertran, François; Jeng, Horng-Tay; Kondo, Takeshi; Kaminski, Adam; Lin, Hsin; Liu, Zheng; Song, Fengqi; Shin, Shik; Hasan, M. Zahid

    2016-08-15

    It has recently been proposed that electronic band structures in crystals can give rise to a previously overlooked type of Weyl fermion, which violates Lorentz invariance and, consequently, is forbidden in particle physics. It was further predicted that Mo x W 1 - x Te 2 may realize such a type-II Weyl fermion. Here, we first show theoretically that it is crucial to access the band structure above the Fermi level ε F to show a Weyl semimetal in Mo x W 1 - x Te 2 . Then, we study Mo x W 1 - x Te 2 by pump-probe ARPES and we directly access the band structure > 0.2 eV above ε F in experiment. By comparing our results with ab initio calculations, we conclude that we directly observe the surface state containing the topological Fermi arc. We propose that a future study of Mo x W 1 - x Te 2 by pump-probe ARPES may directly pinpoint the Fermi arc. Our work sets the stage for the experimental discovery of the first type-II Weyl semimetal in Mo x W 1 - x Te 2 .

  18. CoRoT photometry and STELLA spectroscopy of an eccentric, eclipsing, and spotted HgMn binary with sub-synchronized rotation

    Science.gov (United States)

    Strassmeier, K. G.; Granzer, T.; Mallonn, M.; Weber, M.; Weingrill, J.

    2017-01-01

    Context. We report the discovery and analysis of very narrow transits in the eccentric spectroscopic binary HSS 348 (IC 4756). Aims: The aim is to characterize the full HSS 348 system. Methods: We obtained high-precision CoRoT photometry over two long runs and multi-epoch high-resolution échelle spectroscopy and imaging with STELLA. Standard radial-velocity extraction, spectrum synthesis, Fourier analysis, and light-curve inversions are applied to the data. Results: HSS 348 is found to be an eccentric (e = 0.18) double-lined spectroscopic binary with a period of 12.47 d in which at least the primary component is a peculiar B star of the HgMn class. The orbital elements are such that the system undergoes a grazing eclipse with the primary in front but no secondary eclipse. The out-of-eclipse light variations show four nearly equidistant but unequal minima stable in shape and amplitude throughout our observations. Their individual photometric periods are all harmonics of the same fundamental period which happens to agree with the transit period to within the errors. We interpret the fundamental period to be the rotation period of at least one if not both stars due to surface inhomogeneities. Due to the non-zero eccentricity of the orbit the two components are rotating sub-synchronously. Conclusions: It appears that HSS 348 is not a member of the IC 4756 cluster but a background B8+B8.5 binary system. Its sharp eclipses every 12.47 days just mimic a small-body transit but are in reality the grazing eclipses of a B-star binary and thus a classical false positive. The system seems to be pre-main sequence with the primary possibly just arrived on the ZAMS. The light curve with four unequal minima can be explained with four cool spots of different size equidistantly positioned in longitude. Our data do not allow to uniquely assign the spots to either of the two stars. The CoRoT space mission, launched on 2006 December 27, has been developed and is operated by CNES, with

  19. Multiple superconducting states induced by pressure in Mo>3mn>Sb>7mn>

    Energy Technology Data Exchange (ETDEWEB)

    Feng, Yejun; Wang, Yishu; Palmer, A.; Li, Ling; Silevitch, D. M.; Calder, S.; Rosenbaum, T. F.

    2017-03-01

    Tuning competing ordering mechanisms with hydrostatic pressure in the 4 d intermetallic compound Mo 3 Sb 7 reveals an intricate interplay of structure, magnetism, and superconductivity. Synchrotron x-ray diffraction and magnetic susceptibility measurements, both employing diamond anvil cell technologies, link a first-order structural phase transition to a doubling of the superconducting transition temperature. In contrast to the spin-dimer picture for Mo 3 Sb 7 , we deduce from x-ray absorption near-edge structure and dc magnetization measurements at ambient pressure that Mo 3 Sb 7 should possess only very small, itinerant magnetic moments. The pressure evolution of the superconducting transition temperature strongly suggests its enhancement is due to a difference in the phonon density-of-states with changed crystal symmetry.

  20. Anomalies in the Charge Yields of Fission Fragments from the U<mo stretchy='false'>(mo>n,f stretchy='false'>)mo>>238mn> Reaction

    Energy Technology Data Exchange (ETDEWEB)

    Wilson, J. N.; Lebois, M.; Qi, L.; Amador-Celdran, P.; Bleuel, D.; Briz, J. A.; Carroll, R.; Catford, W.; De Witte, H.; Doherty, D. T.; Eloirdi, R.; Georgiev, G.; Gottardo, A.; Goasduff, A.; Hadyńska-Klęk, K.; Hauschild, K.; Hess, H.; Ingeberg, V.; Konstantinopoulos, T.; Ljungvall, J.; Lopez-Martens, A.; Lorusso, G.; Lozeva, R.; Lutter, R.; Marini, P.; Matea, I.; Materna, T.; Mathieu, L.; Oberstedt, A.; Oberstedt, S.; Panebianco, S.; Podolyák, Zs.; Porta, A.; Regan, P. H.; Reiter, P.; Rezynkina, K.; Rose, S. J.; Sahin, E.; Seidlitz, M.; Serot, O.; Shearman, R.; Siebeck, B.; Siem, S.; Smith, A. G.; Tveten, G. M.; Verney, D.; Warr, N.; Zeiser, F.; Zielinska, M.

    2017-06-01

    Fast-neutron-induced fission of 238 U at an energy just above the fission threshold is studied with a novel technique which involves the coupling of a high-efficiency γ -ray spectrometer (MINIBALL) to an inverse-kinematics neutron source (LICORNE) to extract charge yields of fission fragments via γ - γ coincidence spectroscopy. Experimental data and fission models are compared and found to be in reasonable agreement for many nuclei; however, significant discrepancies of up to 600% are observed, particularly for isotopes of Sn and Mo. This indicates that these models significantly overestimate the standard 1 fission mode and suggests that spherical shell effects in the nascent fission fragments are less important for low-energy fast-neutron-induced fission than for thermal neutron-induced fission. This has consequences for understanding and modeling the fission process, for experimental nuclear structure studies of the most neutron-rich nuclei, for future energy applications (e.g., Generation IV reactors which use fast-neutron spectra), and for the reactor antineutrino anomaly.

  1. Synthesis of CeFe10.5Mo1.5 with ThMn12-type structure by melt spinning

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, C; Tessema, M; Meyer, MS; Pinkerton, FE

    2013-06-01

    Rare earth compounds RFe12_xMx with tetragonal ThMn12-type structure are of great research interest for potential applications as permanent magnets. These materials are known to serve as the precursors for nitriding and hydriding processes which in certain conditions can dramatically increase the Curie temperature, spontaneous magnetization, and affect the magnetic anisotropy. In this paper, we report the phase study of CeFe10.5Mo1.5 samples melt spun at various surface wheel speeds vs between 5 m/s and 60 m/s. The results from quantitative Rietveld analysis indicate that the as-spun ribbons are a mixture of primary CeFe10.5Mo1.5 phase with impurity phases such as Ce2Fe17, Fe-Mo alloy and CeFe2. When the wheel speed vs is below 25 m/s, CeFe10.5Mo1.5 phase accounts for greater than 85 wt% in the as-spun ribbons, while the Fe-Mo alloy is the only detectable impurity phase. Above v(s)=25 m/s, as the wheel speed increases, CeFe10.5Mo1.5 phase decreases monotonically to about 60 wt% at v(s)=6O m/s while the amounts of impurity phases increase. Thermogravimetric measurement indicates that the Curie temperature T-c. corresponding to CeFe10.5Mo1.5 phase is 341 K. As a result, the best performing sample melt spun at v(s),=15 m/s only exhibits an energy product BHmax=0.121 MGOe at room temperature. Although such a number is modest for a permanent magnet, further nitriding is expected to greatly enhance the Curie temperature, and hence the magnetic performance. (C) 2013 Elsevier B.V. All rights reserved.

  2. Nanoporous magnets of chiral and racemic [{Mn(HL)}2Mn{Mo(CN)7}2] with switchable ordering temperatures (TC = 85 K 106 K) driven by H2O sorption (L = N,N-dimethylalaninol).

    Science.gov (United States)

    Milon, Julie; Daniel, Marie-Christine; Kaiba, Abdellah; Guionneau, Philippe; Brandès, Stéphane; Sutter, Jean-Pascal

    2007-11-14

    Molecule-based solids represent a rare opportunity to combine, adjust, and interrelate structural and physical functionalities to develop multifunctional materials. Here we report on a series of porous supramolecular magnets whose magnetic properties are related to their sorption state. A family of magnets of the formula [{Mn(HL)(H2O)}2Mn{Mo(CN)7}2].2H2O have been obtained by assembling the heptacyano-metalate building unit {Mo(CN)7}4- with Mn(II) in the presence of protonated N,N-dimethylalaninol (L) as ligand, the latter being either as a racemic mixture or as a chiral R- or S-enantiomer. The resulting magnets possess an open framework structure and exhibit a TC with a switching behavior (TC = 85 K 106 K) as a function of the hydration state. Moreover, chiral magnets are formed with the optically active ligands. The H2O and gas (N2, CO2, CO) sorption features, the magnetic behavior of both the hydrated and dehydrated magnets, and the crystal structures of the hydrated chiral (S) and racemic magnets are described.

  3. Stoichiometry, thickness and crystallinity of MOCVD grown Hg{sub 1x-y}Cd{sub x}Mn{sub y}Te determined by nuclear techniques of analysis

    Energy Technology Data Exchange (ETDEWEB)

    Studd, W.B.; Johnston, P.N.; Bubb, I.F. [Royal Melbourne Inst. of Tech., VIC (Australia); Leech, P.W. [Applied Research and Developement, Telecom Australia, Clayton, VIC (Australia)

    1993-12-31

    The quaternary semi-conductor Hg{sub 1-x-y}Cd{sub x}Mn{sub y}Te has been grown by Metal Organic Chemical Vapour Deposition using the Interdiffused Multi-layer Process. The layers have been analysed by Ion beam (PIXE, RBS, channeling) and related analytical techniques (EDXRF, XRD, RHEED) to obtain stoichiometric and structural information. The analysis shows that all four elements are present throughout the layer and that the elemental concentrations and thickness of the layer vary considerably over the film. Channeling, XRD and RHEED have been combined to show that the layer is polycrystalline. 14 refs., 3 figs.

  4. High Temperature Wear Characteristics of Paste Boron-aluminized Layer on 5CrMnMo Steel%5CrMnMo钢膏剂硼铝共渗层的高温磨损特性

    Institute of Scientific and Technical Information of China (English)

    陈九磅; 刘少光; 束德林; 郭新成

    2001-01-01

    In this paper,the high temperature wear characteristics of paste boron-aluminized layer on 5CrMnMo steel were investigated.It has been shown that fatigue-spalling is the main wear mechanism,abrasive wear also exist.The spalling cracks are initiated from microporosity,cavity,etc.existing in the cases,then are propagated by the cyclic mechanical stress and the cyclic thermal stress.%研究了5CrMnMo钢膏剂硼铝共渗层的高温磨损特性。结果表明,渗层磨损机制以疲劳剥落为主,兼有磨粒磨损。剥落裂纹源于渗层中疏松、孔洞等缺陷处,并在周期机械应力和周期热应力作用下扩展。

  5. RE-nitrocarburizing Technology for Piston Rod Made of 40CrMnMo%40CrMnMo活塞连杆稀土离子氮碳共渗工艺

    Institute of Scientific and Technical Information of China (English)

    匡建新; 汪新衡; 赵虎军; 朱航生

    2009-01-01

    Some ion RE-nitrocarbnrizing tests were carried out on the 40CrMnMo steel piston rod with different temperature,time,gas pressure and RE content.The surface micro-hardness and the depth of strengthened layers were determined and the wear resistance and bending fatigue strength were compared with other surface treatments.The results show that the optimum parameters are of that the RE content is 5wt%,the treating temperature,time and gas pressure are 520 ℃,2 h and 1.05 kPa,respectively.The 40CrMnMo steel piston rod treated with this technology can completely meet the quality requirement used in high speed supercharge diesel engine.%对40CrMnMo钢制活塞连杆试样进行不同温度、时间、气压及稀土含量下的稀土离子氮碳共渗工艺试验,测定了不同工艺参数下表面强化层的硬度、厚度,并对比了稀土离子氮碳共渗工艺与其他表面强化工艺处理后的磨损性能和弯曲疲劳强度等力学性能.结果表明:5%RE、520℃×2 h、1.05 kPa气压为该工艺的最佳参数.40CrMnMo钢制高速增压柴油机活塞连杆用该工艺处理后,完全能满足其使用性能要求.

  6. 07MnNiCrMoVDR钢在硫化氢溶液中的腐蚀疲劳裂纹扩展速率数学模型%Crack Growth Rate of 07MnNiCrMoVDR Steel in H2S Solution

    Institute of Scientific and Technical Information of China (English)

    纪冬梅; 周昌玉; 胡毓仁

    2005-01-01

    The corrosion fatigue characteristics of 07MnNiCrMoVDR steel in H2S are studied in this paper. Experiments on corrosion fatigue crack growth rate are carried out. On the basis of the experimental data, the crack growth rates under the different environments are predicted with the neural network. The network is trained with the three main influence factors, that is, the solution concentration, the loading frequency and the stress ratio as the input nodes, and the crack growth rate coefficient C as the output node. On the basis of the datum predicted by the trained network, the relationship between the crack growth rate and these three influence factors is obtained.Then the mathematical model of the crack growth rate of 07MnNiCrMoVDR steel in H2S solution is obtained by regression.%本文通过试验研究07MnNiCrMoVDR钢在硫化氢水溶液中的腐蚀疲劳裂纹扩展特性,根据试验数据,利用神经网络,以介质浓度、载荷频率、应力比作为输入节点,裂纹扩展速率系数C作为输出节点,训练该网络预测不同条件下的裂纹扩展速率.根据由神经网络所预测的数据找出这三个影响因素在裂纹扩展速率系数C中的关系表达式,从而回归出07MnNiCrMoVDR钢在硫化氢水溶液中的腐蚀疲劳裂纹扩展速率数学模型.

  7. ZEOLITAS NaY INTERCAMBIADAS CON METALES DE TRANSICIÓN (Fe2+, Co2+, Mo2+, Mn2+ COMO CATALIZADORES PARA LA OXIDACIÓN DE LIMONENO

    Directory of Open Access Journals (Sweden)

    Nubia Quiroz Prada

    2010-08-01

    Full Text Available Se obtuvieron zeolitas NaMY (M = Fe2+, Co2+, Mn2+, Mo2+ y NaCoMoY, las cuales fueron caracterizadas por espectrometría de absorción atómica, difracción de rayos X y análisis termogravimétrico. Estas zeolitas se ensayaron como catalizadores en la oxidación de R-(+-limoneno por oxígeno molecular y yodosilbenceno. El análisis por cromatografía de gases de alta resolución reveló que los principales productos de oxidación fueron los 1,2-epóxilimonenos, en relación molar cis/trans = 2. Otros productos mayoritarios fueron la carvona y los isómeros geométricos del carveol, en relación cis/trans = 0.5. Como resultado del intercambio iónico, se obtuvieron concentraciones de alrededor de un ion de Fe2+, Mn2+, Co2+ o Mo2+ por celda unitaria en las zeolitas NaMY. Estas zeolitas exhibieron actividad catalítica en la oxidación del limoneno. Los iones Co2+ y Fe2+ mostraron la mayor actividad. Las zeolitas NaCoMoY también fueron buenos catalizadores de esta oxidación, pero no se observaron efectos significativos de cooperación entre los dos metales.

  8. Preparation of Mo-Re-C samples containing Mo7Re13C with the β-Mn-type structure by solid state reaction of planetary-ball-milled powder mixtures of Mo, Re and C, and their crystal structures and superconductivity

    Science.gov (United States)

    Oh-ishi, Katsuyoshi; Nagumo, Kenta; Tateishi, Kazuya; Takafumi, Ohnishi; Yoshikane, Kenta; Sugiyama, Machiko; Oka, Kengo; Kobayashi, Ryota

    2017-01-01

    Mo-Re-C compounds containing Mo7Re13C with the β-Mn structure were synthesized with high-melting-temperature metals Mo, Re, and C powders using a conventional solid state method with a planetary ball milling machine instead of the arc melting method. Use of the ball milling machine was necessary to obtain Mo7Re13C with the β-Mn structure using the solid state method. Almost single-phase Mo7Re13C with a trace of impurity were obtained using the synthesis method. By XRF and lattice parameter measurements on the samples, Fe element existed in the compound synthesized using the planetary ball milling machine with a pot and balls made of steel, though Fe element was not detected in the compound synthesized using a pot and balls made of tungsten carbide. The former compound containg the Fe atom did not show superconductivity but the latter compound without the Fe atom showed superconductivity at 6.1 K.

  9. 焊接工艺对40CrMnMo小齿轮补焊抗裂性的影响%The Influence of Welding Technology to CrackResistance of Forged Steel 40CrMnMo Pinion Defects Welding Repair

    Institute of Scientific and Technical Information of China (English)

    李家森; 赵宏明

    2014-01-01

    The cracks about forged steel 40CrMnMo pinion was introduced , and the weldability of 40CrMnMo was analyzed . Take defects welding repair of forged steel 40CrMnMo Pinion for example , the connection between the welding technology and the crack resistance was expounded .Pointed out that the welding technology has a direct impact to improve carack resistance , only compiled reasonable welding technology to ensure welding quality .%本文介绍了锻钢40CrMnMo 小齿轮裂纹情况,分析了40CrMnMo 的焊接性,以40CrMnMo小齿轮补焊为例,阐述了焊接工艺与抗裂性的关系。指出焊接工艺对提高抗裂性有直接影响,只有制定合理的焊接工艺才能确保焊接质量。

  10. Synthesis of CeFe{sub 10.5}Mo{sub 1.5} with ThMn{sub 12}-type structure by melt spinning

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Chen, E-mail: chen.1.zhou@gm.com [MEDA Engineering and Technical Services LLC, 17515 W 9 Mile Road Suite 1075, Southfield, MI 48075 (United States); Tessema, Misle [Optimal CAE Inc., 14492 N. Sheldon Road, Suite 300, Plymouth, MI 48170 (United States); Meyer, Martin S.; Pinkerton, Frederick E. [Chemical and Materials Systems Lab, General Motors R and D Center, 30500 Mound Road, Warren, MI 48090 (United States)

    2013-06-15

    Rare earth compounds RFe{sub 12−x}M{sub x} with tetragonal ThMn{sub 12}-type structure are of great research interest for potential applications as permanent magnets. These materials are known to serve as the precursors for nitriding and hydriding processes which in certain conditions can dramatically increase the Curie temperature, spontaneous magnetization, and affect the magnetic anisotropy. In this paper, we report the phase study of CeFe{sub 10.5}Mo{sub 1.5} samples melt spun at various surface wheel speeds v{sub s} between 5 m/s and 60 m/s. The results from quantitative Rietveld analysis indicate that the as-spun ribbons are a mixture of primary CeFe{sub 10.5}Mo{sub 1.5} phase with impurity phases such as Ce{sub 2}Fe{sub 17}, Fe–Mo alloy and CeFe{sub 2}. When the wheel speed v{sub s} is below 25 m/s, CeFe{sub 10.5}Mo{sub 1.5} phase accounts for greater than 85 wt% in the as-spun ribbons, while the Fe–Mo alloy is the only detectable impurity phase. Above v{sub s}=25 m/s, as the wheel speed increases, CeFe{sub 10.5}Mo{sub 1.5} phase decreases monotonically to about 60 wt% at v{sub s}=60 m/s while the amounts of impurity phases increase. Thermogravimetric measurement indicates that the Curie temperature T{sub c} corresponding to CeFe{sub 10.5}Mo{sub 1.5} phase is 341 K. As a result, the best performing sample melt spun at v{sub s}=15 m/s only exhibits an energy product BH{sub max}=0.121 MGOe at room temperature. Although such a number is modest for a permanent magnet, further nitriding is expected to greatly enhance the Curie temperature, and hence the magnetic performance. - Highlights: ► We synthesize CeFe{sub 10.5}Mo{sub 1.5} with ThMn{sub 12}-type structure by melt spinning. ► Melt spinning dramatically reduces the synthesis time from weeks to hours. ► The as-spun CeFe{sub 10.5}Mo{sub 1.5} ribbons are multiphasic. ► A lower wheel speed v{sub s}≤25 m/s favors the formation of CeFe{sub 10.5}Mo{sub 1.5} phase.

  11. A comparative study on improved Arrhenius-type and artificial neural network models to predict high-temperature flow behaviors in 20MnNiMo alloy.

    Science.gov (United States)

    Quan, Guo-zheng; Yu, Chun-tang; Liu, Ying-ying; Xia, Yu-feng

    2014-01-01

    The stress-strain data of 20MnNiMo alloy were collected from a series of hot compressions on Gleeble-1500 thermal-mechanical simulator in the temperature range of 1173 ∼ 1473 K and strain rate range of 0.01 ∼ 10 s(-1). Based on the experimental data, the improved Arrhenius-type constitutive model and the artificial neural network (ANN) model were established to predict the high temperature flow stress of as-cast 20MnNiMo alloy. The accuracy and reliability of the improved Arrhenius-type model and the trained ANN model were further evaluated in terms of the correlation coefficient (R), the average absolute relative error (AARE), and the relative error (η). For the former, R and AARE were found to be 0.9954 and 5.26%, respectively, while, for the latter, 0.9997 and 1.02%, respectively. The relative errors (η) of the improved Arrhenius-type model and the ANN model were, respectively, in the range of -39.99% ∼ 35.05% and -3.77% ∼ 16.74%. As for the former, only 16.3% of the test data set possesses η-values within ± 1%, while, as for the latter, more than 79% possesses. The results indicate that the ANN model presents a higher predictable ability than the improved Arrhenius-type constitutive model.

  12. LaFe{sub x}Mn{sub y}Mo{sub z}O{sub 3} catalysts for the oxidation of volatile aromatic organic contaminants

    Energy Technology Data Exchange (ETDEWEB)

    Tristao, Juliana C.; Lago, Rochel M. [Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG (Brazil). Dept. de Quimica; Ardisson, Jose D.; Macedo, Waldemar A.A. [Centro de Desenvolvimento de Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil). Lab. de Fisica Aplicada; Moura, Flavia C.C. [Universidade Federal de Ouro Preto (UFOP), MG (Brazil). Dept. de Quimica]. E-mail: flaviamoura@iceb.ufop.br

    2007-07-01

    New mixed perovskites LaFe{sub x}Mn{sub y}Mo{sub z}O{sub 3} were prepared, characterized and investigated as catalysts for the total oxidation of the model aromatic VOC (Volatile Organic Compound), toluene. The perovskites were characterized by XRD (X-Ray Diffractometry), Moessbauer spectroscopy, TPR (Temperature Programmed Reduction) and BET surface area determination. The results suggested the formation of the perovskite phase with incorporation of all metals in the structure. The catalytic studies were carried out in a Temperature Programmed Reaction system with toluene (1000 ppm) and synthetic air in the gas phase. It was observed that the oxidation of toluene starts at temperature as low as 280 deg C and that Mn is responsible for most of the catalytic activity. However, the presence of small amounts of Fe (LaFe{sub 0.27}Mn{sub 0.73}O{sub 3}) leads to an increase in this activity. Stability studies showed that these perovskite catalysts are stable even after 100 h reaction at 400 deg C with no significant structural change, as observed by XRD and Moessbauer analyses. (author)

  13. Dehydrogenation of propane in the presence of CO{sub 2} over polyacid chromium oxide catalysts modified by Mo, W and Mn

    Energy Technology Data Exchange (ETDEWEB)

    Lapidus, A.L.; Agafonov, Yu.A.; Gaidai, N.A.; Nekrasov, N.V.; Davydov, P.E. [Russian Academy of Sciences, Moscow (Russian Federation). N.D. Zelinsky Institute of Organic Chemistry

    2013-11-01

    Effective chromium oxide catalysts without additions and with addition of Mo, W and Mn were prepared and tested in long-duration experiments for propane dehydrogenation in the presence of CO{sub 2}. The optimal concentrations of metals were found. It was shown that the best combination of acid-base and redox properties necessary for a decrease of aggregation of chromium-oxide particles was observed over the following catalyst: (3.0 wt.%Cr-1.5 wt.% Mn)/SiO{sub 2}. This catalyst worked stably in durable tests (500 h). Mechanism of propane oxidative dehydrogenation was studied using unstationary response method. It was shown that the process mechanism was similar over all studied catalysts but the catalysts were differed by the adsorption capacity of the reaction components: CO{sub 2} was tied more firmly than C{sub 3}H{sub 6} over Cr and Cr-Mn, C{sub 3}H{sub 6} was tied more strongly than CO{sub 2} over Cr-W. The reverse water-gas shift reaction proceeded in more extent over chromium-oxide catalysts without additions. (orig.)

  14. Electronic structures and properties of eight-coordinate metal-polyarsenic complexes MAs8n- (M = V, Nb, Ta, Cr, Mo, W, Mn, Tc, Re).

    Science.gov (United States)

    Li, J; Wu, K

    2000-04-03

    The eight-coordinate early transition metal polyarsenic complexes, MAs(8)3- (M = V, Nb, Ta), MAs(8)2- (M = Cr, Mo, W), and MAs8- (M = Mn, Tc, Re), have been studied using density functional theory (DFT). The geometry optimizations of these complexes indicate that in the most stable structures the transition metal atoms are trapped in a crownlike cavity consisting of a zigzag eight-membered ring of As8 cluster. The scalar-relativistic effects and spin-orbit coupling effects on the electronic structures and energy levels were taken into account. The stabilities of gas-phase MAs8n- ions and bonding between the As8 ring and early transition metals are discussed on the basis of population analysis, atomization energies, and decomposition reaction energies. All these complex ions are found to be diamagnetic with notable HOMO-LUMO energy gaps. The vibrational frequencies and infrared absorption intensities of the MAs8n- series are predicted theoretically. Brief theoretical calculations of the similar MoA(8)2- pnictide ions indicate that the analogous P, Sb, and even Bi complexes are likely to be stable, whereas the crownlike MoN(8)2- is not a stable complex.

  15. Some positive effects of introducing Pt4+ and Fe3+ to the MnMo-oxide anode deposited on IrO2/Ti substrate for best oxygen evolution efficiency during electrolysis in 0.5 M NaCl solution

    Directory of Open Access Journals (Sweden)

    R.M. Abou Shahba

    2013-06-01

    Full Text Available NaCl solution (0.5 M of pH 2 was electrolyzed at 1000 Am−2 at room temperature. Addition of Pt4+ and Fe3+ to the prepared MnMo-oxide anode deposited on IrO2/Ti substrate, significantly improves the performance of anode for the oxygen evolution reaction (OER during NaCl electrolysis. After 2000 h of electrolysis, the oxygen evolution efficiency (OEE is in the order of MnMoPt-oxide > MnMoFe-oxide > MnMo-oxide anodes with 100%, 99%, and 93.2% OEE, respectively. The loss in weight of MnMo-oxide is reduced from about 13% to 3.2% and 0.0% by addition of iron and platinum cations, to the deposition electrolyte. The mean average grain size of MnO2, MnMo-, MnMoFe- and MnMoPt-oxide deposits prepared in electrolytes of pH 0.0 are in the range of 25.5, 16.22, 13.5 ∼ 16.5 and 13 ∼ 17.5 nm, respectively. The physicochemical properties of the deposits were characterized using X-ray diffraction spectroscopy (XRD, energy dispersive X-ray spectroscopy (EDX, scanning electron microscopy (SEM and electrochemical techniques. EDX analysis illustrates that IrO2/Ti is stable during the deposition process and behaves only as conductive substrate. SEM illustrates that, all elements constituting MnMoPt- and MnMoFe-oxide deposits are homogeneously distributed in the oxide surface.

  16. Spectroscopic, thermal and biological studies of coordination compounds of sulfasalazine drug: Mn(II), Hg(II), Cr(III), ZrO(II), VO(II) and Y(III) transition metal complexes

    Indian Academy of Sciences (India)

    M G Abd El-Wahed; M S Refat; S M El-Megharbel

    2009-04-01

    The complexations of sulfasalazine (H3Suz) with some of transition metals have been investigated. Three types of complexes, [Mn(HSuz)-2(H2O)4].2H2O, [M(HSuz)-2(H2O)2].H2O (M = Hg(II), ZrO(II) and VO(II), = 4, 8 and 6, respectively) and [M(HSuz)-2(Cl)(H2O)3].H2O (M = Cr(III) and Y(III), = 5 and 6, respectively) were obtained and characterized by physicochemical and spectroscopic methods. The IR spectra of the complexes suggest that the sulfasalazine behaves as a monoanionic bidentate ligand. The thermal decomposition of the complexes as well as thermodynamic parameters ( *}, *, * and *) were estimated using Coats–Redfern and Horowitz–Metzger equations. In vitro antimicrobial activities of the H3Suz and the complexes were tested.

  17. Influence of welding parameters on nitrogen content in welding metal of 32Mn-7Cr-1Mo-0.3N austenitic steel

    Institute of Scientific and Technical Information of China (English)

    FU Rui-dong; QIU Liang; WANG Cun-yu; WANG Qing-feng; ZHENG Yang-zeng

    2005-01-01

    The transfer behavior of nitrogen into the welding metal during gas tungsten arc welding process of 32Mn-7Cr-1Mo-0.3N steel was investigated. The effects of gas tungsten arc welding process variables, such as the volume fraction of nitrogen in shielding gas, arc holding time and arc current on the nitrogen content in the welding metal were also evaluated. The results show that the volume fraction of nitrogen in gas mixture plays a major role in controlling the nitrogen content in the welding metal. It seems that there exhibits a maximum nitrogen content depending on the arc current and arc holding time. The optimum volume fraction of nitrogen in shielding gas is 4% or so. The role of gas tungsten arc welding processing parameters in controlling the transfer of nitrogen is further confirmed by the experimental results of gas tungsten arc welding process with feeding metal.

  18. Effect of cold deformation on pitting corrosion of 00Cr18Mn15Mo2N0.86 stainless steel for coronary stent application.

    Science.gov (United States)

    Ren, Yibin; Zhao, Haochuan; Liu, Wenpeng; Yang, Ke

    2016-03-01

    The high nitrogen nickel-free stainless steel has offered an alternative to further improve the performance of the coronary stents, and simultaneously avoids the potential harms of nickel element. Both cold deformation and pitting corrosion are very important for coronary stents made of stainless steel. In this work, the effect of cold deformation on the pitting corrosion resistance of a high nitrogen nickel-free stainless steel (00Cr18Mn15Mo2N0.86) in 0.9% saline solution was investigated. The results showed that the pitting corrosion of the steel was nearly unchanged with increases of the cold deformation up to 50%, indicating that the higher nitrogen content can reduce the negative effect of cold deformation on the pitting corrosion resistance, which is beneficial for the long term service of coronary stents in blood vessel.

  19. Chemical Coupling SERS Properties of Pyridine on Silver-Caged Metal Clusters M@Ag12 (M = V-, Nb-, Ta-, Cr, Mo, W, Mn+, Tc+, Re+)

    Science.gov (United States)

    Chen, Lei; Wang, Zhigang; Li, Zhengqiang; Zhang, Rui-Qin

    2017-07-01

    Using density functional theory, this work presents a comprehensive analysis of nonresonant surface-enhanced Raman scattering enhancement of pyridine on M@Ag12 (M = V-, Nb-, Ta-, Cr, Mo, W, Mn+, Tc+, Re+). Computational results indicate that the chemical enhancement of pyridine on M@Ag12 is closely associated with the charge properties of silver-caged clusters. Pyridine on negative clusters exhibits the strongest chemical enhancement with a factor of about 103, while the chemical enhancement is only about 102 for pyridine on neutral clusters and 10 for pyridine on positive clusters. The polarizability analyses elucidate the nature of the chemical enhancement that delocalized electrons of negative adsorption systems occupy higher molecular orbitals than those of neutral and positive adsorption systems, which can lead to stronger nonresonant chemical enhancement.

  20. Fracture toughness evaluation of 20MnMoNi55 pressure vessel steel in the ductile to brittle transition regime: Experiment & numerical simulations

    Science.gov (United States)

    Gopalan, Avinash; Samal, M. K.; Chakravartty, J. K.

    2015-10-01

    In this work, fracture behaviour of 20MnMoNi55 reactor pressure vessel (RPV) steel in the ductile to brittle transition regime (DBTT) is characterised. Compact tension (CT) and single edged notched bend (SENB) specimens of two different sizes were tested in the DBTT regime. Reference temperature 'T0' was evaluated according to the ASTM E1921 standard. The effect of size and geometry on the T0 was studied and T0 was found to be lower for SENB geometry. In order to understand the fracture behaviour numerically, finite element (FE) simulations were performed using Beremin's model for cleavage and Rousselier's model for ductile failure mechanisms. The simulated fracture behaviour was found to be in good agreement with the experiment.

  1. Critical behavior of amorphous Fe80 - xMxB14Si6 alloys with M=Mo, V, Mn, and 2 <= x <= 14

    Science.gov (United States)

    Jen, S. U.; Lee, C. C.; Huang, P. L.; Lin, S. T.

    1990-05-01

    Amorphous Fe80-xMxB14Si6 alloys with M=Mo, V, Mn, and 2≤x≤14 have been made by the rapid quenching method. The critical exponents β, γ, δ, and Tc were determined by two independent methods: the method of Kouvel-Fisher and the scaling plot. With the addition of M, β, and γ deviate more from the values predicted by the three-dimensional Heisenberg model, and are closer to the values proposed by Sobotta and Wagner. δ remains less changed. The magnetic inhomogeneity of these alloys is evidenced by the specific heat, the forced magnetoresistance, and the Mössbauer measurements. By increasing x, the peak of specific heat becomes smeared and less divergent, and forced magnetoresistance changes from negative to positive around Tc.

  2. Chemical Coupling SERS Properties of Pyridine on Silver-Caged Metal Clusters M@Ag12 (M = V-, Nb-, Ta-, Cr, Mo, W, Mn+, Tc+, Re+)

    Science.gov (United States)

    Chen, Lei; Wang, Zhigang; Li, Zhengqiang; Zhang, Rui-Qin

    2016-10-01

    Using density functional theory, this work presents a comprehensive analysis of nonresonant surface-enhanced Raman scattering enhancement of pyridine on M@Ag12 (M = V-, Nb-, Ta-, Cr, Mo, W, Mn+, Tc+, Re+). Computational results indicate that the chemical enhancement of pyridine on M@Ag12 is closely associated with the charge properties of silver-caged clusters. Pyridine on negative clusters exhibits the strongest chemical enhancement with a factor of about 103, while the chemical enhancement is only about 102 for pyridine on neutral clusters and 10 for pyridine on positive clusters. The polarizability analyses elucidate the nature of the chemical enhancement that delocalized electrons of negative adsorption systems occupy higher molecular orbitals than those of neutral and positive adsorption systems, which can lead to stronger nonresonant chemical enhancement.

  3. Research of Luminescence Properties on MO-RE2 O3 -B2 O3:Eu, Mn(M=Mg, Ca, Sr; RE=Y, La, Gd)

    Institute of Scientific and Technical Information of China (English)

    Liang Zhongyi; He Dawei; Shi Yanning

    2004-01-01

    A series of phosphor of MO-RE2 O3-B2 O3: Eu, Mn ( M = Mg, Ca, Sr; RE = Y, La, Gd) were prepared and studied.Excitation spectra exhibited high absorption in UV region (370 ~ 400 nm).There existed two valence states for europium ions Eu2+ and Eu 3+, the broad emission band peaking at 515 nm correspond to the 5d-4f emission transition of Eu2+ , the sharp emission peaking at 590 and 610 nm correspond to the 5D0→7FJ(J = 1,2,3,4) emission transition of Eu 3 + By the introduction of Mg and Y into MO-RE2O3-B2O3: Eu, blue-green emission was restrained ultimately and red emission peaking at 610 nm was enhanced strongly, intensity and colorimetric purity of red light were both enhanced.Furthermore, Mg1-xSrxO-Y2O3-B2O3: Eu was also researched, the introduction of Sr into MgO-Y2O3-B2O3:Eu gives rise to a shift to longer wavelengths of the position of the excitation peak, and the emission spectra varies with the increasing of x simultaneously.

  4. AZ91 D镁合金Mo-Mn无铬转化膜的制备与耐蚀性%Preparation and Corrosion Resistance of Mo-Mn Chromium-free Conversion Coating Formed on AZ91 D Magnesium Alloys

    Institute of Scientific and Technical Information of China (English)

    朱青; 朱明; 余勇; 张路路

    2015-01-01

    ABSTRACT:Objective To improve the surface corrosion resistance of AZ91D magnesium alloy by Mo-Mn chromium-free conver-sion coating. Methods Effects of different concentrations of NaMoO4 and KMnO4 and temperature on the transformed sample film were studied by orthogonal experimental method. After optimizing experiment parameters, the effects of the time on the conversion film was also studied. The morphology and component of conversion coatings were researched by SEM and EDS. Moreover, the po-larization curves and electrochemical impedance spectroscopy of conversion coating were tested in 3. 5%NaCl aqueous solution. Results The results showed that when the condition was 10 g/L NaMoO4 , 6 g/L KMnO4 at 50 ℃ and pH 5 for 40 min, where the morphology of the sample was relatively even and the amount of cracks was relatively low. Compared to the corrosion resistance of magnesium substrate, the corrosion potential of conversion film was increased by about 0. 075 V ,and the corrosion current density decreased by nearly 1 order of magnitude. When the condition was 20 g/L NaMoO4 , 8 g/L KMnO4 at 50 ℃ and pH 5 for 40 min, the morphology of the sample was the most even and the amount of cracks was the least. Compared to the corrosion resistance of magnesium substrate, the corrosion potential of conversion film was increased by about 0. 047 V ,and the corrosion current density decreased by nearly 2 orders of magnitude. EIS showed that the polarization resistance of the latter conversion film sample was 1450. 2 Ω, while the polarization resistance of magnesium matrix was 806. 4 Ω. Conclusion Mo-Mn chromium-free conversion coating could obviously improve the surface corrosion resistance of AZ91D magnesium alloy.%目的:通过Mo-Mn无铬转化膜提高AZ91 D镁合金的表面耐蚀性。方法采用正交实验法,研究不同浓度的NaMoO4和KMnO4以及温度对转化膜的影响。优选实验参数后,考察时间对转化膜的影响。利用SEM及EDS研究转化膜

  5. Influence of the addition of transition metals (Cr, Zr, Mo) on the properties of MnOx-FeOx catalysts for low-temperature selective catalytic reduction of NOx by Ammonia.

    Science.gov (United States)

    Zhou, Changcheng; Zhang, Yaping; Wang, Xiaolei; Xu, Haitao; Sun, Keqin; Shen, Kai

    2013-02-15

    The co-precipitation and citric acid methods were employed to prepare MnO(x)-FeO(x) catalysts for the low-temperature selective catalytic reduction (SCR) of NO(x) by ammonia. It was found that the Mn-Fe (CP) sample obtained from the co-precipitation method, which exhibited low crystalline of manganese oxides on the surface, high specific surface area and abundant acid sites at the surface, had better catalytic activity. The effects of doping different transition metals (Mo, Zr, Cr) in the Mn-Fe (CP) catalysts were further investigated. The study suggested that the addition of Cr can obviously reduce the take-off temperature of Mn-Fe catalyst to 90°C, while the impregnation of Zr and Mo raised that remarkably. The texture and micro-structure analysis revealed that for the Cr-doped Mn-Fe catalysts, the active components had better dispersion with less agglomeration and sintering and the largest BET surface specific area. In situ FTIR study indicated that the addition of Cr can increase significantly the surface acidity, especially, the Lewis acid sites, and promote the formation of the intermediate -NH(3)(+). H(2)-TPR results confirmed the better low-temperature redox properties of Mn-Fe-Cr.

  6. Mechanical characteristics and swelling of austenitic Fe-Cr-Mn steels irradiated in the SM-2 and BOR-60 reactors. [0. 4C-12Cr-19Mn-2Ni-Mo-N; 0. 4C-12Cr-14Mn-5Ni-Mo-2Al-B; 0. 4C-17Cr-17Mn-Cu-Mo-Nb-N; Fe-Cr-Ni steel: 0. 8C-16Cr-15Ni-3Mo-Nb; 316; 304

    Energy Technology Data Exchange (ETDEWEB)

    Shamardin, V.K.; Bulanova, T.M.; Neustroev, V.S. (Lenin (V.I.) Research Inst. of Atomic Reactors, Dimitrovgrad (USSR)); Ivanov, L.I.; Djomina, E.V.; Platov, Yu.M. (AN SSSR, Moscow (USSR). A.A. Baikov Inst. of Metallurgy)

    Three types of austenitic Fe-Cr-Mn stainless steels were irradiated simultaneously with Fe-Cr-Ni austenitic steel at temperatures from 400 to 800deg C in the mixed spectrum of the high flux SM-2 reactor to 10 dpa and 700 appm of He and in the BOR-60 reactor to 60 dpa without He generation. The paper presents the swelling and mechanical properties of steels irradiated in the BOR-60 and SM-2 as a function of the concentration of transmuted He and the value of atomic displacement. (orig.).

  7. Synthesis and Structural Characterization of Manganese Carbonyl Incorporated Polyoxomolybdate (n-Bu4N)2[Mo6O16(OCH3)2 {HOCH2C(CH2O)3}2{Mn(CO)3}2

    Institute of Scientific and Technical Information of China (English)

    WANG Jing-ping; LI Ji-li; NIU Jing-yang

    2008-01-01

    The polyoxoanion incorporated {Mn(CO)3+} complex,(n-Bu4N)2[Mo6O16(OCH3)2{HOCH2C(CH2O)3}2{Mn(CO)3}2](1),has been synthesized by the reaction of (n-Bu4N)4[MosO26] with Mn(CO)sBr in methanol,in the presence of C(CH2OH)4.The complex 1 has been characterized by IR UV-Vis,X-ray single crystal diffraction,and TG.Crystal data for the complex 1:C25H48MnMo3NO16 (1),Triclinic P1,a=0.9405(3) nm,b=1.3351 (4) nm,c=1.5455(4) nm,a=103.206(5)°,β=102.165(5)°,γ=100.784(5)°,V=1.7896(9) nm3,Z=2,R1=0.0703,wR2 = 0.1495.The structure analysis of complex 1 shows that the complex consists of two tetrabutylammonium cations and a polyoxomolybdate anion that incorporates two fac-Mn(CO)3+ units.The anion of complex 1 can be considered as the dimer of two rhomb-like anions by sharing of two comers.

  8. Effect of pH Value on Structure and Properties of Anodic Electrodeposited Mn-MoOxide%pH值对阳极电沉积Mn-Mo氧化物结构与性能的影响

    Institute of Scientific and Technical Information of China (English)

    史艳华; 赵杉林; 梁平; 王玲; 关学雷

    2016-01-01

    By correction to the thermodynamic calculation based on E0‐pH diagram of MnSO4‐SO2 -4 ‐H2 O plating system ,effective pH value range for anodic electrodeposition of M nO 2 phase structure materials got clear ,at 363K ,with Mn2+ concentration 0 .2mol · dm -3 .The influence law of the pH values was also obtained based on the characterization of the oxide structure and test of its electro‐chemical performance .The results show that pH value in the 0 .33‐3 .4 range ,with its increase and accordingly the conducive to the effective deposition of MnO2 type Mn‐Mo oxide .However ,although with pH value increasing ,deposition efficiency improves ,the coating quality gets degraded ,especially making the electrocatalytic performance of the oxide obviously deteriorated .It also shows that with pH value of plating solution 0 .5 ,obtained Mn‐Mo oxide has excellent coating quality and high electro‐catalytic activity .The reason is closely related to competition in oxygen evolution reaction during the preparation of the oxide .When pH value is small ,oxygen evolution reaction competition causes the solid‐liquid interface stirring ,the dendritic grow th of oxide gets inhabited and the diffusion layer gets thinning ,w hich promotes the nucleation of oxide on the electrode micro‐surface and makes grain re‐fined ,so as to improves the electrocatalytic performance of oxide .%通过热力学计算修正的 M nSO4‐SO2-4‐H2 O镀液体系平衡电势 E0‐pH图,明确了363K和 M n2+浓度0.2mol · dm -3时M nO2物相结构材料阳极电沉积有效pH值范围,通过对氧化物结构表征及电化学性能测试获得了pH值的影响规律。结果表明:pH值在0.33~3.4时,随着pH值增大,有利于MnO2物相结构Mn‐Mo氧化物的有效析出,但pH值增大虽可提高阳极电沉积效率,却造成镀层质量变差,电催化性能明显劣化,镀液pH=0.5时获得的Mn‐Mo氧化物具有优异的镀层质量和高

  9. LaMn{sub 1-x} Fe{sub x} O{sub 3} and LaMn{sub 0.1-x} Fe{sub 0.90} Mo{sub x} O{sub 3} perovskites: synthesis, characterization and catalytic activity in H{sub 2}O{sub 2} reactions

    Energy Technology Data Exchange (ETDEWEB)

    Magalhaes, Fabiano; Lago, Rochel Montero [Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG (Brazil). Dept. de Quimica; Moura, Flavia Cristina Camilo [Universidade Federal de Ouro Preto (UFOP), MG (Brazil). Dept. de Quimica; Ardisson, Jose Domingos [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil). Lab. de Fisica Aplicada

    2008-07-01

    In this work two perovskites were prepared: LaMn{sub 1-x} Fe{sub x} O{sub 3}, and LaMn{sub 0.1-x} Fe{sub 0.90} Mo{sub x} O{sub 3}. XRD and Moessbauer spectroscopy suggest the formation of pure phase perovskite with the incorporation of Fe and Mo in the structure. The catalytic activity of these materials was studied in two reactions with H{sub 2}O{sub 2}: the decomposition to O{sub 2}, and the oxidation of the model organic contaminant methylene blue. The perovskite composition strongly affects the catalytic activity, while Fe decreases the H{sub 2}O{sub 2} decomposition Mo strongly improves dye oxidation. (author)

  10. 20CrMnMo钢渗碳齿轮磨削裂纹成因分析%Causes Analysis on Grinding Cracks of 20CrMnMo Steel Carburized Gears

    Institute of Scientific and Technical Information of China (English)

    孙胜伟; 宋亚虎; 刘铁山; 史向阳; 赵学谦

    2016-01-01

    采用化学成分分析、金相分析、显微硬度测试以及残余应力测定等方法对某 2 0 CrMnMo钢渗碳齿轮磨削裂纹产生原因进行了分析.结果表明:该齿轮产生磨削裂纹主要是由于磨削过程中表面产生严重的二次淬火烧伤和回火烧伤,二次淬火烧伤的次表面及边缘回火烧伤区硬度大幅下降及表面受拉应力,两者共同作用下产生了磨削裂纹;另外,渗碳层中存在针状马氏体和大量残余奥氏体,增加了齿轮磨削开裂的敏感性,这是齿轮产生磨削裂纹的另一个重要原因.%The forming reasons for grinding cracks of 20CrMnMo steel carburized gears were analyzed by means of chemical composition analysis,metallographic examination,microhardness test and residual stress test. The results show that the main reasons for the grinding cracks were secondary quenching burn and tempering burn on the gear surface during grinding.Grinding cracks were caused by the combined effects of serious decline in hardness and surface tensile stress at the subsurface of the secondary quenching burn area and the edge tempering burn area.Besides,the grinding cracking sensitivity was increased due to the acicular martensite and massive retained austenite existing in the carburized layer,which was also an important reason for the grinding cracks.

  11. Chromium-free conversion coatings based on inorganic salts (Zr/Ti/Mn/Mo) for aluminum alloys used in aircraft applications

    Energy Technology Data Exchange (ETDEWEB)

    Santa Coloma, P., E-mail: patricia.santacoloma@tecnalia.com [TECNALIA Research & Innovation, Parque Tecnológico de San Sebastián, Mikeletegi Pasealekua 2, E-20009 Donostia-San Sebastián, Gipuzkoa (Spain); Izagirre, U.; Belaustegi, Y.; Jorcin, J.B.; Cano, F.J. [TECNALIA Research & Innovation, Parque Tecnológico de San Sebastián, Mikeletegi Pasealekua 2, E-20009 Donostia-San Sebastián, Gipuzkoa (Spain); Lapeña, N. [Boeing Research & Technology Europe, S.L.U., Avenida Sur del Aeropuerto de Barajas 38, Building 4 – 3rd Floor, E-28042 Madrid (Spain)

    2015-08-01

    Highlights: • Chromium-free conversion coatings for corrosion protection of aluminum alloys. • Salt spray and potentiodynamic sweep tests to study the corrosion behavior. • Local deposits on Cu-rich intermetallic particles enhanced corrosion resistance. • Surface characterization to relate bath's composition and corrosion resistance. • Best corrosion protection with conversion baths without titanium salts. - Abstract: Novel chromium-free conversion coatings based on Zr/Ti/Mn/Mo compounds were developed at a pilot scale to improve the corrosion resistance of the AA2024-T3 and AA7075-T6 aluminum alloys for aircraft applications. The influence of the presence of Zr and Ti in the Zr/Ti/Mn/Mo conversion bath's formulation on the corrosion resistance of the coated alloys was investigated. The corrosion resistance provided by the conversion coatings was evaluated by salt spray exposure and potentiodynamic sweeps. Optical and scanning electron microscopy coupled with energy dispersive spectroscopy (SEM/EDS) and atomic force microscopy (AFM) operating in the Kelvin Probe mode (SKPFM) were used to provide microstructural information of the coated samples that achieved the best results in the corrosion tests. The salt spray test evidenced the higher corrosion resistance of the coated samples compared to the bare surfaces for both alloys. The potentiodynamic tests showed that the corrosion current density decreased for coated AA7075-T6 and AA2024-T3 alloys, which indicated an obvious improvement of the corrosion resistance with all the processes for both alloys. Although the corrosion resistance of the coated samples appeared to be higher for the alloy AA7075-T6 than for the alloy AA2024-T3, both alloys achieved the best corrosion protection with the coatings deposited from conversion bath formulations containing no titanium salts. The microscopy analysis on the coated AA7075-T6 samples revealed that a local deposition of Zr compounds and, possibly, an

  12. Phase evolution in Fe-Cr-Mn-Mo powders processed by mechanical alloying in N{sub 2} atmosphere

    Energy Technology Data Exchange (ETDEWEB)

    Mancha, H.; Mendoza, G.; Belmares, S.; Escalante, J.I.; Mendez, M. [Cinvestav-Saltillo, Mex. (Mexico); Cisneros, M.M. [Inst. Tecnologico de Saltillo (Mexico); Lopez, H. [Univ. of Wisconsin, Milwaukee, Dept. of Materials Engineering, WI (United States)

    2001-07-01

    Nanostructured Fe-18Cr-11Mo-xN alloys were prepared by attrition milling of elemental powders under N{sub 2} atmosphere for different times. It was found that the amount of nitrogen present in the powder mixture increased up to 1.6 wt% after 192 h. As-milled powders were encapsulated in quartz tubes and heat treated at 1173 and 1473 K to promote austenisation. Different phases were identified posterior to crystallization namely, ferrite, austenite and Cr{sub 2}N, which occurred in different amounts depending on the nitrogen content and the heat-treatment temperature. No nitrogen desorption was perceptible after the crystallization annealing treatment. The results showed that it is feasible to obtain a fully austenitic structure by controlling the processing parameters. (orig.)

  13. The Microstructure and Properties of Low-Carbon PM Mn-Cr-Mo Steels Sintered under Different Conditions

    Directory of Open Access Journals (Sweden)

    Sułowski M.

    2014-06-01

    Full Text Available W artykule przedstawiono wpływ parametrów spiekania na mikrostrukturę i własności mechaniczne spiekanych, niskowęglowych stali manganowo-chromowo-molibdenowych. W pracy wykazano, że własności mechaniczne stali wykonanej na bazie proszku stopowego Astaloy CrL (l,5%Cr, 0,2%Mo, reszta Fe spiekanej w temperaturze 1250°C w atmosferze 5%H2-95%N2 nie zależą od temperatury odpuszczania, czego nie stwierdzono podczas badań własności wytrzymałościowych tych stali wy- twarzanych w niższej temperaturze spiekania (1120°C. Ponadto, prowadzone badania wykazały, że stale wytworzone na bazie proszku stopowego Astaloy CrM (3%Cr, 0,5%Mo. reszta Fe po spiekaniu w temperaturze 1250°C w atmosferze powietrza charakteryzowały się porównywalnymi lub wyższymi własnościami mechanicznymi niż stale wykonane na bazie proszku sto- powego Astaloy CrL, wytwarzane w tych samych warunkach. Podczas spiekania w powietrzu zastosowano odłamkowe cząstki żelazomanganu o łącznej masie 52 g, które umieszczano w bezpośrednim sąsiedztwie próbek (całkowita masa próbek 490 g w stalowej łódce, w celu redukcji tlenków. Jak wykazały badania, dodatek żelazomanganu był niewystarczający, aby zapewnić kompletną redukcję tlenków.

  14. A New Resource-Saving, High Chromium and Manganese Super Duplex Stainless Steels 29Cr-12Mn-2Ni-1Mo-xN

    Institute of Scientific and Technical Information of China (English)

    MA Zheng-huan; ZHAO Xiang-juan; GE Chang-sheng; DING Tie-suo; LI Jun; XIAO Xue-shan

    2011-01-01

    A new family of resource saving, high chromium and manganese super duplex stainless steels (DSSs), with a composition in mass percent, % of Cr 0.29, Mn 0.12, Ni 2.0, Mo i. 0, and N 0. 51-0. 68, has been developed by examining the effect of N on the microstructure, mechanical properties and corrosion properties. The results show that these alloys have a balanced ferrite-austenite relation. The austenite volume fraction decreases with the solution treatment temperature, but it increases with an increase in N content. The increases in nitrogen enhance the ultimate tensile strength (UTS) and reduce the ductility of the material slightly. The pitting corrosion potential increases first and then decreases with an increase in nitrogen content when the amount of N arrives to 0.68%. The yield stress and ultimate tensile strength of solution treated samples were more than 680 and 900 MPa, the elongation of experimental alloys are higher than 30%, respectively, what is more, the pitting potentials were beyond 1 100 mV.

  15. Strain-dependent ferroic properties of doped LaMO{sub 3}(M=Mn or Co) and BiFeO{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Doerr, Kathrin; Rata, Diana; Herklotz, Andreas; Bilani, Orkidia; Dekker, Martina; Schultz, Ludwig [IFW Dresden, Postfach 270116, 01171 Dresden (Germany); Reibold, Marianne [Technische Universitaet Dresden, Speziallabor Triebenberg, 01328 Dresden (Germany); Biegalski, Michael; Christen, Hans [Oak Ridge National Laboratory, CNMS, PO Box 2008, Bethel Valley Rd., Oak Ridge, TN 37831 (United States)

    2010-07-01

    Elastic strain at epitaxially grown interfaces provides an efficient coupling mechanism in two-phase multiferroics: piezoelectric or magnetostrictive strain arising from application of an electric or a magnetic field is transferred readily between the components. We employ a piezoelectric single-crystalline substrate to apply reversible biaxial strain to epitaxially grown magnetic or ferroelectric films and study the strain response of their ferroic properties. The relaxor-based 0.72PbMg{sub 1/3}Nb{sub 2/3}O{sub 3} -0.28PbTiO{sub 3}(001) (PMN-PT) proved to be a favourable piezo-substrate with large, reversible, uniform in-plane strain which shows little temperature dependence. The magnetization vs. strain of doped LaMO{sub 3} (M=Mn or Co) phases has been studied. It reveals the impact of the strain-induced tetragonal lattice distortion on the ferromagnetic double exchange and the magnetic moment of Co ions that leads to moderate or large magnetization modulation. Further, the strain dependence of ferroelectric switching has been investigated for multiferroic BiFeO{sub 3}. It displays a large response of unexpected sign attributed to a strain influence on kinetics.

  16. Photodiodes based in La0.7Sr0.3MnO3/single layer MoS2 hybrid vertical heterostructures

    Science.gov (United States)

    Niu, Yue; Frisenda, Riccardo; Svatek, Simon A.; Orfila, Gloria; Gallego, Fernando; Gant, Patricia; Agraït, Nicolás; Leon, Carlos; Rivera-Calzada, Alberto; Pérez De Lara, David; Santamaria, Jacobo; Castellanos-Gomez, Andres

    2017-09-01

    The fabrication of artificial materials by stacking of individual two-dimensional (2D) materials is amongst one of the most promising research avenues in the field of 2D materials. Moreover, this strategy to fabricate new man-made materials can be further extended by fabricating hybrid stacks between 2D materials and other functional materials with different dimensionality making the potential number of combinations almost infinite. Among all these possible combinations, mixing 2D materials with transition metal oxides can result especially useful because of the large amount of interesting physical phenomena displayed separately by these two material families. We present a hybrid device based on the stacking of a single layer MoS2 onto a lanthanum strontium manganite (La0.7Sr0.3MnO3) thin film, creating an atomically thin device. It shows a rectifying electrical transport with a ratio of 103, and a photovoltaic effect with V oc up to 0.4 V. The photodiode behaviour arises as a consequence of the different doping character of these two materials. This result paves the way towards combining the efforts of these two large materials science communities.

  17. Characterization of Precipitation Behavior and Fracture Toughness along Thickness Direction in SA508 Gr.3 Mn-Mo-Ni low alloy steels

    Energy Technology Data Exchange (ETDEWEB)

    Song, Jaemin; Kim, Min-Chul; Hong, Seokmin; Lee, Bong-Sang [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2015-10-15

    SA 508 Gr.3 Mn-Mo-Ni low alloy steel forgings thicker than 200 mm are used for reactor pressure vessels in nuclear power plants. The cooling rate difference along the thickness direction during the quenching process causes variation in the microstructure and mechanical properties. The microstructural variation and its influence on the fracture toughness of RPV steels were investigated in this study. The cleavage fracture toughness in the transition region were evaluated with the ASTM E1921 master curve method for samples at different locations from the inner surface to the center thickness of the RPV steel. The microstructural features, such as the area fraction, and the size and distribution of precipitates were quantitatively evaluated at each sampling position. Microstructure observations showed that at near the surface position, bainite laths are finer, and furthermore, the carbides are smaller and homogeneously distributed. The fracture toughness at the surface was better than those at deeper positions. The reference temperature T{sub 0} showed a linear relationship with the area fraction of the carbides bigger than a certain critical size. It is concluded that the size of the precipitates caused by the cooling rate gradient may have a dominant role in controlling the cleavage fracture toughness variation along the thickness direction for a very thick RPV steel.

  18. Prediction of two-dimensional diluted magnetic semiconductors: Doped monolayer MoS2 systems

    KAUST Repository

    Cheng, Yingchun

    2013-03-05

    Using first-principles calculations, we propose a two-dimensional diluted magnetic semiconductor: monolayer MoS2 doped by transition metals. Doping of transition metal atoms from the IIIB to VIB groups results in nonmagnetic states, since the number of valence electrons is smaller or equal to that of Mo. Doping of atoms from the VIIB to IIB groups becomes energetically less and less favorable. Magnetism is observed for Mn, Fe, Co, Zn, Cd, and Hg doping, while for the other dopants from these groups it is suppressed by Jahn-Teller distortions. Analysis of the binding energies and magnetic properties indicates that (Mo,X)S2 (X=Mn, Fe, Co, and Zn) are promising systems to explore two-dimensional diluted magnetic semiconductors.

  19. Research on tests and numerical analysis of corrosion and wear damage of mooring chain steel 22MnCrNiMo%海洋系泊链钢22MnCrNiMo 腐蚀磨损试验与数值分析研究

    Institute of Scientific and Technical Information of China (English)

    粟京; 刘刚; 孙佳君

    2015-01-01

    A numerical analysis method is proposed to calculate accumulative damages of corrosion and wear of chain link in service period.Both the corrosion of chain annulus in seawater environment and the wear of contact surface between adjacent links can be considered by using non-linear finite element analy-sis.For determining mechanical properties of the chain steel used in the finite element analysis,mechani-cal tests with the low-carbon and low-alloy steel 22MnCrNiMo are carried out to obtain its material hard-ness,seawater erosion and corrosion wear resistance.Numerical results and experimental data are com-pared to verify the feasibility and accuracy of the proposed method.%建立了锚链在海洋环境中腐蚀磨损(简称“磨蚀”)累积损伤数值分析方法,该方法采用非线性有限元分析,能够同时考虑锚链链环间接触面在海水中的腐蚀和磨损耦合损伤。针对22MnCrNiMo 低碳低合金钢材料,进行了力学性能、海水侵蚀以及磨蚀性能等多方面的试验研究,确定了基于该材料的锚链链环间接触面在海水中磨蚀损伤数值分析中的相关参数。通过对计算结果与试验结果的比较分析,验证了锚链链环间接触面磨蚀累积损伤数值分析方法的可行性与准确性。

  20. Studies on stability and capacity for long-life cycle performance of Li(Ni0.5Co0.2Mn0.3)O2 by Mo modification for lithium-ion battery

    Science.gov (United States)

    Zhang, Yin; Wang, Zhen-Bo; Yu, Fu-Da; Que, Lan-Fang; Wang, Min-Jun; Xia, Yun-Fei; Xue, Yuan; Wu, Jin

    2017-08-01

    Long-life property is one of the key factors for wide applications of lithium-ion batteries. Here, Mo-modified Ni-rich cathode material LiNi0.5Co0.2Mn0.3O2 (NCM) is synthesized successfully via a solvent evaporating way followed with a calcination method. This strategy delivers two kinds of effects including Mo-doping and Mo-coating. Mo not only intercalates into the crystal lattice of NCM, but also forms a film-like coating layer on the surface to impede side reactions between electrode and electrolyte. Thus, its specific capacity, rate capability and cycle performance are improved simultaneously, especially in terms of long cycling life property. A series of physical and electrochemical characterizations are used to study the modified performance, and the sample with 1.0 wt% Mo modifying presents the best property with an approximate 3.5 nm coating layer surrounding the surface. Besides, the capacity retention ratio reaches to 89.7% even after 500 cycles between 3.0 and 4.3 V. However, Mo-modified samples have an obvious attenuation in the later period after charging to a higher voltage of 4.6 V although they have preferable cycle performance at the preliminary stage. The results indicate that the reaction mechanisms are diverse at different voltage ranges, which may guide subsequent researches.

  1. Structural study of CaMn{sub 1−x}Mo{sub x}O{sub 3} (0.08 ≤ x ≤ 0.12) system by neutron powder diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Supelano, G.I., E-mail: ivan.supelano@uptc.edu.co [Grupo Física de Materiales, Escuela de Física, Universidad Pedagógica y Tecnológica de Colombia, Tunja (Colombia); Parra Vargas, C.A.; Barón-González, A.J. [Grupo Física de Materiales, Escuela de Física, Universidad Pedagógica y Tecnológica de Colombia, Tunja (Colombia); Sarmiento Santos, A. [Grupo Superficies Electroquímica y Corrosión, Escuela de Física, Universidad Pedagógica y Tecnológica de Colombia, Tunja (Colombia); Frontera, C. [Institut de Ciència de Materials de Barcelona, CSIC, Campus Universitari de Bellaterra, E-08193, Bellaterra, Barcelona (Spain)

    2016-08-15

    Neutron powder diffraction experiments and magnetic measurements in polycrystalline CaMn{sub 1−x}Mo{sub x}O{sub 3} (x = 0.08, 0.10, 0.12) point towards a possible charge and orbital order in this system. The analysis of structural and magnetic data show that the samples present structural phase transformation from Pnma to P2{sub 1}/m space group and the system has a C-type antiferromagnetic configuration at low temperature. A detailed analysis of the bond distances signals a small Jahn-Teller distortion of only one (x = 0.08) or of the two Mn ions (x = 0.10, 0.12). We identify the partially occupied e{sub g} orbitals and this explains the C-type magnetic structure. - Highlights: • CaMn{sub 1−x}Mo{sub x}O{sub 3} (x = 0.08, 0.10, 0.12) is investigated by neutron powder diffraction. • Analysis of individual Mn-O distances demonstrates the apparition of orbital order. • By symmetry analysis, we find that the low temperature magnetic structure is C-type. • Magnetic interactions foreseen by the orbital order explain the magnetic structure.

  2. 渗碳温度对22Si2MnCrNi2MoA钢渗碳层的影响%Influence of carburizing temperature on microstructure and properties of carburized layers of a 22Si2MnCrNi2MoA steel

    Institute of Scientific and Technical Information of China (English)

    黄斌; 朱洪武; 杨忠; 周乐育; 刘雅政

    2013-01-01

    Influence of carburizing temperature on carburized layers of a 22Si2MnCrNi2MoA steel solid-carburized was studied by OM,SEM,XRD and hardness measurements.The relationship between carburizing temperature and carbon concentration,micro-hardness and retained austenite of the carburized layers were examined.The results indicate that with the carburizing temperature increasing for carburizing time of 6 h,the carbon concentration of the carburized layers gradually increases,and the distribution gradient of the carbon concentration gets smoother.The relationship between the micro-hardness of the carburized layers and carbon concentration obeys normal distribution.It is recommended that the surface carbon concentration of the carburized steel should be controlled in the range of 0.80% and 0.90% in order to obtain martensite microstructure with high hardness.When the surface carbon concentration is more than 0.80%-0.90%,aging treatment for a long time or deep cryogenic treatment are required to remove retained austenite in the carburized layers.%通过固体渗碳试验研究了加热温度对钎具用钢22Si2MnCrNi2MoA渗碳层的影响,分析了渗碳温度-碳浓度-显微硬度-残留奥氏体的关系以及残留奥氏体的控制措施.结果表明:当渗碳时间为6h时,随着渗碳温度的升高,渗碳层的碳浓度逐渐增加,碳浓度分布梯度越来越平缓.22Si2MnCrNi2MoA钢渗碳层的显微硬度-碳浓度关系符合正态分布.在渗碳处理过程中,为了使渗碳表层获得硬度很高的马氏体组织,22Si2MnCrNi2MoA钢渗碳层表面碳浓度应该控制在0.80% ~0.90%之间.当表面碳浓度超过0.80%~0.90%时,渗碳完成后需采取后续的工艺措施来消除已经存在的残留奥氏体,如采用长时间自然时效或深冷处理等.

  3. Optimization of the Arc Spraying Process Parameters of the Fe–Base Mn-Si-Cr-Mo-Ni Coatings for the Best Wear Performance

    Directory of Open Access Journals (Sweden)

    Justinas GARGASAS

    2016-05-01

    Full Text Available In this paper, the use of Fe–base Mn-Si-Cr-Mo-Ni and Fe–base Mn-Si-Cr wires for thermal arc spraying is presented. For this purpose the mechanical and physical properties of coatings were evaluated. The quality of the coating’s was dependent on the selected equipment, spray materials, technological parameters of the spray and spray technology. The aim was to qualify and optimize the parameters for spray coating to get the best coatings properties with good tribological properties. All coatings were deposited on mild steel S235JR substrates. Two experimental cored wires of unique chemical composition – STEIN-MESYFIL 932 V and STEIN-MESYFIL 954 V – were used for thermal arc spraying. The wires of 1.6 mm diameter were used for the surfacing material. Hardness, porosity and oxide measurements were used to verify the spray parameters and analyze the coatings. Rubber wheel test, which is based on the standard ASTM G65, was used. Dry-sand, rubber-wheel procedure according ASTM G65 was used to investigate low stress abrasion, whereas for high stress abrasion investigations a rubber wheel was used. This experiment was carried out by changing the speed of disc friction, travel distance and measuring the mass loss of surface friction. Miller Test according to ASTM G75-95 Standard was carried out in experiment with friction. The samples were immersed in water with corundum and polished with 22 N load, for 8 hours. Furthermore a correlation was performed between the spraying current and voltage parameter. The coatings’ cross sections were examined using scanning electron microscope (SEM and optical microscopy. The influence of the composite components of the coatings’ microstructure, such as porosity, microhardness, oxide inclusions, on the tribological properties of thermal sprayed coatings is discussed in this paper. DOI: http://dx.doi.org/10.5755/j01.ms.22.1.7339

  4. Optimization of the Arc Spraying Process Parameters of the Fe–Base Mn-Si-Cr-Mo-Ni Coatings for the Best Wear Performance

    Directory of Open Access Journals (Sweden)

    Justinas GARGASAS

    2016-05-01

    Full Text Available In this paper, the use of Fe–base Mn-Si-Cr-Mo-Ni and Fe–base Mn-Si-Cr wires for thermal arc spraying is presented. For this purpose the mechanical and physical properties of coatings were evaluated. The quality of the coating’s was dependent on the selected equipment, spray materials, technological parameters of the spray and spray technology. The aim was to qualify and optimize the parameters for spray coating to get the best coatings properties with good tribological properties. All coatings were deposited on mild steel S235JR substrates. Two experimental cored wires of unique chemical composition – STEIN-MESYFIL 932 V and STEIN-MESYFIL 954 V – were used for thermal arc spraying. The wires of 1.6 mm diameter were used for the surfacing material. Hardness, porosity and oxide measurements were used to verify the spray parameters and analyze the coatings. Rubber wheel test, which is based on the standard ASTM G65, was used. Dry-sand, rubber-wheel procedure according ASTM G65 was used to investigate low stress abrasion, whereas for high stress abrasion investigations a rubber wheel was used. This experiment was carried out by changing the speed of disc friction, travel distance and measuring the mass loss of surface friction. Miller Test according to ASTM G75-95 Standard was carried out in experiment with friction. The samples were immersed in water with corundum and polished with 22 N load, for 8 hours. Furthermore a correlation was performed between the spraying current and voltage parameter. The coatings’ cross sections were examined using scanning electron microscope (SEM and optical microscopy. The influence of the composite components of the coatings’ microstructure, such as porosity, microhardness, oxide inclusions, on the tribological properties of thermal sprayed coatings is discussed in this paper. DOI: http://dx.doi.org/10.5755/j01.ms.22.1.7339

  5. Mossbauer and XRD characterization of the phase transformations in a Fe-Mn-Al-C-Mo-Si-Cu as cast alloy during tribology test

    Energy Technology Data Exchange (ETDEWEB)

    Ramos, J. [Universidad Autónoma de Occidente (Colombia); Piamba, J. F. [Universidad del Valle, Departamento Física (Colombia); Sánchez, H. [Universidad del Valle, Escuela de Materiales (Colombia); Alcazar, G. A. Pérez, E-mail: gpgeperez@gmail.com [Universidad del Valle, Departamento Física (Colombia)

    2015-06-15

    In present study Fe-29.0Mn-6Al–0.9C-1.8Mo-1.6Si-0.4Cu (%w) alloy was obtained after melted in an induction furnace, and then molded as an ingot. From the as cast ingot it were cut samples for the different characterization measurements. The microstructure of the as-cast sample is of dendritic type and its XRD pattern was refined with the lines of the austenite, with a big volumetric fraction, and the lines of the martensite, with small volumetric fraction. The Mössbauer spectrum of the sample was fitted with a broad singlet which corresponds to disordered austenite. After the tribology test, its XRD pattern was refined with the lines of two austenite phases, one similar to the previous one and other with bigger lattice parameter. The total volumetric fraction of the austenite is smaller than that obtained for sample without wear. It was added the lines of the martensite phase with bigger volumetric fraction than that of the previous sample. The Mössbauer spectrum of the weared sample was fitted with two paramagnetic sites which correspond to the two Fe austenite phases and a hyperfine magnetic field distribution which is associated to the disordered original martensite and the new one which appears in the surface as a consequence of the wear process. These results show that during wear process the original austenite phase is transformed in martensite and in a new austenite phase. The increases of the martensitic phase improves mechanical properties and wear behavior.

  6. Molybdenum doped Pr0.5Ba0.5MnO3-δ (Mo-PBMO) double perovskite as a potential solid oxide fuel cell anode material

    Science.gov (United States)

    Sun, Yi-Fei; Zhang, Ya-Qian; Hua, Bin; Behnamian, Yashar; Li, Jian; Cui, Shao-Hua; Li, Jian-Hui; Luo, Jing-Li

    2016-01-01

    A layered Mo doped Pr0.5Ba0.5MnO3-δ (Mo-PBMO) double perovskite oxide was prepared by a modified sol-gel method and the properties of the fabricated material are characterized by various technologies. The results of X-ray diffraction (XRD), H2-temperature programmed reduction (H2-TPR), NH3-temperature programmed desorption (NH3-TPD), and thermogravimetric analysis (TGA) demonstrate that the treatment in reducing atmosphere at high temperature lead to a significant phase transformation of the material to a single cubic phase as well as with the Mo in multiple oxidized states. Such character leads to the production of large amount of oxygen deficiency with facilitated oxygen diffusion. The electrochemical performance tests of half-cell and single cell SOFCs exhibit the promoted effect of Mo on catalytic activity for the oxidation of H2 and CH4, indicating that Mo-PBMO could serve as an anode material candidate for SOFCs.

  7. HT300/7CrMnSiMoV双金属复合铸造汽车模具组织性能的研究∗%Microstructure and Properties of Bimetals HT300/7CrMnSiMoV by Compound Casting for Automobile Cover Die

    Institute of Scientific and Technical Information of China (English)

    张福全; 张勇; 周惦武; 郑耀明; 闫旭东

    2016-01-01

    Interface bonding condition,microstructure and mechanical properties of the bimetal casting prepared by liquid-liquid compound casting were characterized by scanning electron microscope(SEM),energy dispersive X-ray spectroscopy(EDS),Instron-3382 tensile testing machine and micro hardness tester.The results showed that HT300/7CrMnSiMoV bimetal steel for automobile cover mold was successfully prepared by reasonable compound casting tech-nology.No microvoid,unbonded region,cracks and other defects were founded at the interface.The composite inter-face was composed of three parts,the steel matrix,the transition region and the iron matrix.The transition region had a zigzag structure with thickness of about 400μm.Cr and Si elements near the interface presented gradient distribu-tion.The two alloys reached a good metallurgical bonding state.The hardness gradually decreased across interface from HT300 to 7CrMnSiMoV and tensile strength of the bimetal reached 339 MPa.Fracture appeared at the side of HT300,and the tensile strength of the bimetal was higher than that of HT300.%采用扫描电镜、显微硬度计、Instron-3382型力学性能试验机等,对双液复合铸造铸件的界面结合情况、微观组织和力学性能进行研究。结果表明:采用合理的铸造生产工艺,成功制备了满足使用性能要求的 HT300/7CrMnSiMoV双金属汽车模具铸件,其复合界面清晰、致密,无明显缩孔、缩松等铸造缺陷;复合界面由钢基体区、过渡区和铁基体区3个区域组成。过渡区呈犬牙状/锯齿形结构,过渡层厚度约为400μm,界面附近Cr和 Si元素呈梯度分布,两种合金冶金结合状态良好;复合界面两侧显微硬度呈梯度分布,其抗拉强度达到339 MPa,断裂位置出现在灰铸铁一侧,双金属界面的结合强度高于灰铸铁。

  8. Magnetic order and electronic properties of Li{sub 2}Mn{sub 2}(MoO{sub 4}){sub 3} material for lithium-ion batteries: ESR and magnetic susceptibility studies

    Energy Technology Data Exchange (ETDEWEB)

    Suleimanov, N.M. [E. K. Zavoisky Physical-Technical Institute of Russian Academy of Sciences, Kazan (Russian Federation); Kazan State Power Engineering University, Kazan (Russian Federation); Prabaharan, S.R.S. [VIT University, School of Electronics Engineering, Chennai (India); Khantimerov, S.M.; Nizamov, F.A. [E. K. Zavoisky Physical-Technical Institute of Russian Academy of Sciences, Kazan (Russian Federation); Michael, M.S. [SSN College of Engineering, Department of Chemistry, Chennai (India); Drulis, H.; Wisniewski, P. [Institute of Low Temperature and Structure Research of Polish Academy of Sciences, Wroclaw (Poland)

    2016-08-15

    We describe the application of electron spin resonance (ESR) and magnetic susceptibility methods to study the magnetic properties and valence state of transition metal ions in Li{sub 2}Mn{sub 2}(MoO4){sub 3} polyanion compound previously studied for its cathode-active properties in lithium containing batteries. ESR measurements of Li{sub 2}Mn{sub 2}(MoO{sub 4}){sub 3} have shown the presence of Mn{sup 2+} ions in the octahedral environment of oxygen ions. It is found that the part of manganese ions occupy the anti-site positions in lithium sublattice. The absence of the ESR signal from molybdenum ions indicates that they are non-magnetic and adopt the 6{sup +} valence state. Considerable overlapping between 3d orbitals of transition metal and 2p oxygen orbitals has been experimentally established. This leads to the indirect exchange interaction and antiferromagnetic ordering of manganese ions at 1.4 K. (orig.)

  9. First-Principles Study on the Structural Stability and Segregation Behavior of γ-Fe/Cr2N Interface with Alloying Additives M (M = Mn, V, Ti, Mo, and Ni

    Directory of Open Access Journals (Sweden)

    Hui Huang

    2016-07-01

    Full Text Available This study investigated the structural stability and electrochemical properties of alloying additives M (M = Mn, V, Ti, Mo, or Ni at the γ-Fe(111/Cr2N(0001 interface by the first-principles method. Results indicated that V and Ti were easily segregated at the γ-Fe(111/Cr2N(0001 interface and enhanced interfacial adhesive strength. By contrast, Ni and Mo were difficult to segregate at the γ-Fe(111/Cr2N(0001 interface. Moreover, the results of the work function demonstrated that alloying additives Mn reduced local electrochemical corrosion behavior of the γ-Fe(111/Cr2N(0001 interface by cutting down Volta potential difference (VPD between clean γ-Fe(111 and Cr2N(0001, while alloying additives V, Ti, Mo, and Ni at the γ-Fe(111/Cr2N(0001 interface magnified VPD between clean γ-Fe(111 and Cr2N(0001, which were low-potential sites that usually serve as local attack initiation points.

  10. Synthesis and electrochemical characterizations of spinel LiMn1.94MO4 (M = Mn0.06, Mg0.06, Si0.06, (Mg0.03Si0.03)) compounds as cathode materials for lithium-ion batteries

    Science.gov (United States)

    Zhao, Hongyuan; Liu, Xingquan; Cheng, Cai; Li, Qiang; Zhang, Zheng; Wu, Yue; Chen, Bing; Xiong, Weiqiang

    2015-05-01

    The spinel LiMn1.94MO4 (M = Mn0.06, Mg0.06, Si0.06, (Mg0.03Si0.03)) compounds are successfully synthesized by citric acid-assisted sol-gel method. The crystal structures and morphologies of synthesized compounds are characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM), respectively. All the compounds possess the cubic spinel structure of LiMn2O4 with space group of Fd-3m. The electrochemical properties of synthesized compounds are investigated by galvanostatic charge-discharge test, cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The results show that the Si-doping can increase the discharge capacity of LiMn2O4 due to the more expanded and regular MnO6 octahedra. In particular, for the LiMn1.94Mg0.03Si0.03O4 compound, the addition of Si4+ ions can make up for the shortage of Mg-doping in term of the discharge capacity. As a result, the Mg2+ and Si4+ co-doping has the effect of synergistic enhancement, which can make full use of the respective advantages of Mg-doping and Si-doping. The optimal LiMn1.94Mg0.03Si0.03O4 can deliver the initial discharge capacity of 128.3 mAh g-1 with good capacity retention of 92.8% after 100 cycles at 0.5 C in the voltage range of 3.20-4.35 V. Compared with the undoped LiMn2O4, the co-doped compound also presents superior rate performance, especially the capacity recovery performance.

  11. PHONON DISPERSION ofFe-18°/oCr-10°/oMn-16°/oNi and Fe-18°/oCr-12°/oNi-2°/oMo ALLOYS

    Directory of Open Access Journals (Sweden)

    Mustafa Özduran

    2006-12-01

    Full Text Available In the present paper, to investigate the. phonon frequencies of face-centered-cubic (f.c.c. Fe-1 8%Cr-1 Oo/oMn-16%Ni andFe-18%Cr-12%Ni-2%Mo a1loys it has been used an empirical many-body potential (MBP developed by Akgün and Uğur,recently. The parametcrs defıning the MBP f.c.c. alloys m ay be computed by following a procedure deseri bed. The radial

  12. Catalytic oxidation of elemental mercury over the modified catalyst Mn/alpha-Al2O3 at lower temperatures.

    Science.gov (United States)

    Li, Jianfeng; Yan, Naiqiang; Qu, Zan; Qiao, Shaohua; Yang, Shijian; Guo, Yongfu; Liu, Ping; Jia, Jinping

    2010-01-01

    In order to facilitate the removal of elemental mercury (Hg(0)) from coal-fired flue gas, catalytic oxidation of Hg(0) with manganese oxides supported on inert alumina (alpha-Al2O3) was investigated at lower temperatures (373-473 K). To improve the catalytic activity and the sulfur-tolerance of the catalysts at lower temperatures, several metal elements were employed as dopants to modify the catalyst of Mn/alpha-Al2O3. The best performance among the tested elements was achieved with molybdenum (Mo) as the dopant in the catalysts. It can work even better than the noble metal catalyst Pd/alpha-Al2O3. Additionally, the Mo doped catalyst displayed excellent sulfur-tolerance performance at lower temperatures, and the catalytic oxidation efficiency for Mo(0.03)-Mn/alpha-Al2O3 was over 95% in the presence of 500 ppm SO2 versus only about 48% for the unmodified catalyst. The apparent catalytic reaction rate constant increased by approximately 5.5 times at 423 K. In addition, the possible mechanisms involved in Hg(0) oxidation and the reaction with the Mo modified catalyst have been discussed.

  13. [N(CH3)4]2[Mn(H2O)]3[Mo(CN)7](2).2H2O: a new high Tc cyano-bridged ferrimagnet based on the [MoIII(CN)7]4- building block and induced by counterion exchange.

    Science.gov (United States)

    Larionova, Joulia; Clérac, Rodolphe; Donnadieu, Bruno; Guérin, Christian

    2002-06-17

    The title compound was synthesized by slow diffusion of aqueous solutions containing K4[Mo(CN)7].2H2O, [Mn(H2O)6](NO3)2, and [N(CH3)4]Cl. The compound crystallized in monoclinic space group C2/c, a = 25.8546(14), b = 12.3906(7), c = 13.5382(7) A, beta = 116.4170 (10) degrees, Z = 4, R = 0.0353, wR2 = 0.0456. The MoIII site is surrounded by six -C-N-Mn linkages and one terminal cyano group in a distorted capped-prism fashion. There are two pentahedral MnII sites in the structure, both with four -N-C-Mo linkages and one water molecule. The anisotropic three-dimensional structure consists of connected corrugated gridlike sheet layers parallel to the bc plane. Tetramethylammonium counterions ([N(CH3)4]+) located between these layers seem to induce their distortion. The three-dimensional organization may also be viewed as interconnected octagonal channels propagated along the c axis. The void space of these channels is occupied by coordinated and crystalized water molecules. Temperature and field dependence of the magnetization in both the dc and ac modes have been measured on polycrystalline sample. These investigations have revealed that the compound ordered ferrimagnetically at Tc = 86 K, with a small hysteresis effect. These findings have been compared to those reported previously for three- and two-dimensional materials of the same family.

  14. Tracing anthropogenic Hg and Pb input using stable Hg and Pb isotope ratios in sediments of the central Portuguese Margin

    NARCIS (Netherlands)

    Mil-Holmens, M.; Blum, J.; Canário, J.; Caetano, M.; Costa, A.M.; Lebreiro, S.M.; Trancoso, M.; Richter, T.O.; de Stigter, H.; Johnson, M.; Branco, V.; Cesário, R.; Mouro, F.; Mateus, M.; Boer, W.; Melo, Z.

    2013-01-01

    Three short marine sediment cores from the Cascais Submarine Canyon (CSC; cores 252-32 and 252-35) and the Estremadura Spur (core 252-16) on the central Portuguese Margin were analysed for Hg, Pb, Al, and Mn concentrations, and both Pb and Hg stable isotope compositions, in order to reconstruct tren

  15. Progress of Research on the Li-rich Cathode Materials xLi2MnO3·(1-x)LiMO2 (M=Co,Fe,Ni1/2Mn1/2…)for Li-ion Batteries%锂离子电池富锂正极材料xLi2MnO3·(1-x)LiMO2(M=Co,Fe,Ni1/2Mn1/2…)的研究进展

    Institute of Scientific and Technical Information of China (English)

    赵煜娟; 冯海兰; 赵春松; 孙召琴

    2011-01-01

    新一代固溶体富锂正极材料xLi2MnO3·(1-x)LiMO2(M=Co,Fe,Ni1/2Mn1/2...)具有高比容量、优秀的循环能力以及新的电化学充放电机制,可能被用做新型高比能量锂离了电池正极材料.本文介绍了富锂正极材料的结构、合成方法、电化学性能研究,探讨了影响其电化学性能的若干因素.并对其进行的各种改性研究进行了概述,分析总结了不同富锂正极材料所具有的特性和发展趋势.%A new generation of Li-rich solid solution materials is cathode material xLi2Mn03.(l-x)LiM02(M= Co, Fe, NiinMn1/2...) because of its excellent electrochemical performance. The series of Li-rich cathode material exhibits high capacity and excellent cycleability, which may be associated with a new electrochemical charge-discharge mechanism, It is proposed to satisfy the high energy Li-ion batteries. The structure, synthesis methods and electrochemical properties of the Li-rich cathode materials were reviewed in this paper. The factors affecting the electrochemical properties of the cathode materials were discussed, and the recent research progress on improving the electrochemical performance of Li-rich cathode materials was summarized. In addition, the characteristics and the trend of different Li-rich cathode materials were described.

  16. Ligand dependence of metal-metal bonding in the d(3)d(3) dimers M(2)X(9)(n-) (M(III) = Cr, Mo, W; M(IV) = Mn, Tc, Re; X = F, Cl, Br, I).

    Science.gov (United States)

    Stranger, R; Turner, A; Delfs, C D

    2001-08-13

    The ligand dependence of metal-metal bonding in the d(3)d(3) face-shared M(2)X(9)(n-) (M(III) = Cr, Mo, W; M(IV) = Mn, Tc, Re; X = F, Cl, Br, I) dimers has been investigated using density functional theory. In general, significant differences in metal-metal bonding are observed between the fluoride and chloride complexes involving the same metal ion, whereas less dramatic changes occur between the bromide and iodide complexes and minimal differences between the chloride and bromide complexes. For M = Mo, Tc, and Re, change in the halide from F to I results in weaker metal-metal bonding corresponding to a shift from either the triple metal-metal bonded to single bonded case or from the latter to a nonbonded structure. A fragment analysis performed on M(2)X(9)(3-) (M = Mo, W) allowed determination of the metal-metal and metal-bridge contributions to the total bonding energy in the dimer. As the halide changes from F to I, there is a systematic reduction in the total interaction energy of the fragments which can be traced to a progressive destabilization of the metal-bridge interaction because of weaker M-X(bridge) bonding as fluoride is replaced by its heavier congeners. In contrast, the metal-metal interaction remains essentially constant with change in the halide.

  17. Effects of alloying elements on fracture toughness in the transition temperature region of base metals and simulated heat-affected zones of Mn-Mo-Ni low-alloy steels

    Science.gov (United States)

    Kim, Sangho; Im, Young-Roc; Lee, Sunghak; Lee, Hu-Chul; Kim, Sung-Joon; Hong, Jun Hwa

    2004-07-01

    This study is concerned with the effects of alloying elements on fracture toughness in the transition temperature region of base metals and heat-affected zones (HAZs) of Mn-Mo-Ni low-alloy steels. Three kinds of steels whose compositions were varied from the composition specification of SA 508 steel (grade 3) were fabricated by vacuum-induction melting and heat treatment, and their fracture toughness was examined using an ASTM E1921 standard test method. In the steels that have decreased C and increased Mo and Ni content, the number of fine M2C carbides was greatly increased and the number of coarse M3C carbides was decreased, thereby leading to the simultaneous improvement of tensile properties and fracture toughness. Brittle martensite-austenite (M-A) constituents were also formed in these steels during cooling, but did not deteriorate fracture toughness because they were decomposed to ferrite and fine carbides after tempering. Their simulated HAZs also had sufficient impact toughness after postweld heat treatment. These findings indicated that the reduction in C content to inhibit the formation of coarse cementite and to improve toughness and the increase in Mo and Ni to prevent the reduction in hardenability and to precipitate fine M2C carbides were useful ways to improve simultaneously the tensile and fracture properties of the HAZs as well as the base metals.

  18. Long-Term Corrosion Testing of Thermal Spray Coatings of Amorphous Metals: Fe49.7Cr17.7Mn1.9Mo7.4W1.6B15.2C3.8Si2.4 and Fe48Mo14Cr15Y2C15B6

    Energy Technology Data Exchange (ETDEWEB)

    Farmer, J; Day, D; Lian, T; Saw, C; Hailey, P; Payer, J; Aprigliano, L; Beardsley, B; Branagan, D

    2007-07-09

    Amorphous alloys identified as SAM2X5 (Fe{sub 49.7}Cr{sub 17.7}Mn{sub 1.9}Mo{sub 7.4}W{sub 1.6}B{sub 15.2}C{sub 3.8}Si{sub 2.4}) and SAM1651 (Fe{sub 48}Mo{sub 14}Cr{sub 15}Y{sub 2}C{sub 15}B{sub 6}) have been produced as melt-spun ribbons, drop-cast ingots and thermal-spray coatings. Chromium (Cr), molybdenum (Mo) and tungsten (W) additions provided corrosion resistance, while boron (B) enabled glass formation. Earlier electrochemical studies of melt-spun ribbons and ingots of these amorphous alloys demonstrated outstanding passive film stability. More recently thermal-spray coatings of these amorphous alloys have been made and subjected to long-term salt-fog and immersion tests. Good corrosion resistance has been observed during salt-fog testing. Corrosion rates were measured in situ with linear polarization, while simultaneously monitoring the open-circuit corrosion potentials. Reasonably good performance was observed. The sensitivity of these measurements to electrolyte composition and temperature was determined. The high boron content of SAM2X5 also made it an effective neutron absorber, and suitable for criticality control applications.

  19. Improved cycling performance of Li{sub 2}MoO{sub 4}-inlaid LiNi{sub 0.5}Co{sub 0.2}Mn{sub 0.3}O{sub 2} cathode materials for lithium-ion battery under high cutoff voltage

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Manfang; Hu, Guorong; Liang, Longwei; Peng, Zhongdong; Du, Ke; Cao, Yanbing, E-mail: cybcsu@csu.edu.cn

    2016-07-15

    Uniform spherical xLi{sub 2}MoO{sub 4}-inlaid LiNi{sub 0.5}Co{sub 0.2}Mn{sub 0.3}O{sub 2} materials were successfully prepared through a solid state synthesis. To investigate the material characterization and electrochemical performance after Li{sub 2}MoO{sub 4} modification, X-ray diffraction (XRD), Rietveld refinement, scanning electron microscopy (SEM), energy dispersive spectrometer (EDS) mapping, transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and electrochemical tests were applied. The results of the XRD, Rietveld refinement, SEM and EDS analyses showed that a Mo atom may be incorporated into the crystal lattice of the layer structure. Moreover, the presence of Li{sub 2}MoO{sub 4} on the LiNi{sub 0.5}Co{sub 0.2}Mn{sub 0.3}O{sub 2} surface was observed. The thickness of the Li{sub 2}MoO{sub 4} coating layer on the xLi{sub 2}MoO{sub 4}-inlaid LiNi{sub 0.5}Co{sub 0.2}Mn{sub 0.3}O{sub 2} material (x = 0.02) was approximately 25 nm. Similarly, XPS was performed to determine the effect of Li{sub 2}MoO{sub 4} modification, confirming the presence of Li{sub 2}MoO{sub 4}. The xLi{sub 2}MoO{sub 4}-inlaid (x = 0.02) LiNi{sub 0.5}Co{sub 0.2}Mn{sub 0.3}O{sub 2} materials exhibited a retention capacity 83.5% higher than that of the bare material (40.9%) after 200 cycles at 0.5 C between 3.0 and 4.4 V, and it also exhibited the best electrochemical properties at a cutoff voltage of 4.5 V. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) confirmed that the modification of Li{sub 2}MoO{sub 4} plays an important role in improving the electrochemical performance of pristine LiNi{sub 0.5}Co{sub 0.2}Mn{sub 0.3}O{sub 2}. - Highlights: • Electrochemical performance of LiNi{sub 0.5}Co{sub 0.2}Mn{sub 0.3}O{sub 2} is improved by Li{sub 2}MoO{sub 4} modification. • Li{sub 2}MoO{sub 4} modification can make the structure of the bare material stable. • Li{sub 2}MoO{sub 4}-inlaid Li[Ni{sub 0.5}Co{sub 0.2}Mn{sub 0.3}]O{sub 2

  20. Experimental bond critical point and local energy density properties determined for Mn-O, Fe-O, and Co-O bonded interactions for tephroite, Mn2SiO4, fayalite, Fe2SiO4, and Co2SiO4 olivine and selected organic metal complexes: comparison with properties calculated for non-transition and transition metal M-O bonded interactions for silicates and oxides.

    Science.gov (United States)

    Gibbs, G V; Downs, R T; Cox, D F; Rosso, K M; Ross, N L; Kirfel, A; Lippmann, T; Morgenroth, W; Crawford, T D

    2008-09-18

    Bond critical point (bcp) and local energy density properties for the electron density (ED) distributions, calculated with first-principle quantum mechanical methods for divalent transition metal Mn-, Co-, and Fe-containing silicates and oxides are compared with experimental model ED properties for tephroite, Mn 2SiO 4, fayalite, Fe 2SiO 4, and Co 2SiO 4 olivine, each determined with high-energy synchrotron single-crystal X-ray diffraction data. Trends between the experimental bond lengths, R(M-O), (M = Mn, Fe, Co), and the calculated bcp properties are comparable with those observed for non-transition M-O bonded interactions. The bcp properties, local total energy density, H( r c), and bond length trends determined for the Mn-O, Co-O, and Fe-O interactions are also comparable. A comparison is also made with model experimental bcp properties determined for several Mn-O, Fe-O, and Co-O bonded interactions for selected organometallic complexes and several oxides. Despite the complexities of the structures of the organometallic complexes, the agreement between the calculated and model experimental bcp properties is fair to good in several cases. The G( r c)/rho( r c) versus R(M-O) trends established for non-transition metal M-O bonded interactions hold for the transition metal M-O bonded interactions with G( r c)/rho( r c) increasing in value as H( r c) becomes progressively more negative in value, indicating an increasing shared character of the interaction as G( r c)/rho( r c) increases in value. As observed for the non-transition metal M-O bonded interactions, the Laplacian, nabla (2)rho( r c), increases in value as rho( r c) increases and as H( r c) decreases and becomes progressive more negative in value. The Mn-O, Fe-O, and Co-O bonded interactions are indicated to be of intermediate character with a substantial component of closed-shell character compared with Fe-S and Ni-S bonded interactions, which show greater shared character based on the | V( r c)|/ G( r c

  1. Methane Oxidation to Synthesis Gas Using Lattice Oxygen of La1-xSrxMO3-λ (M = Fe, Mn) Perovskite Oxides Instead of Molecular Oxygen%La1-xSrxMO3-λ(M=Fe,Mn)氧化物中的晶格氧代替分子氧用于甲烷氧化制取合成气的研究

    Institute of Scientific and Technical Information of China (English)

    李然家; 余长春; 朱光荣; 沈师孔

    2005-01-01

    In this paper, the partial oxidation of methane to synthesis gas using lattice oxygen of La1-xSrxMO3-λ (M=Fe,Mn) perovskite oxides instead of molecular oxygen was investigated. The radox circulation between 11% O2/Ar flow and 11% CH4/He flow at 900℃ shows that methane can be oxidized to CO and H2 with a selectivity of over 90.7% using the lattice oxygen of La1-xSrxFeO3-λ (x≤0.2) perovskite oxides in an appropriate reaction condition, while the lost lattice oxygen can be supplemented by air re-oxidation. It is viable for the lattice oxygen of La1-xSrx FeO3-λ (x≤0.2) perovskite oxides instead of molecular oxygen to react with methane to synthesis gas in the redox mode.

  2. Arsenic and Mn levels in Isaza (Gymnogobius isaza) during the mass mortality event in Lake Biwa, Japan

    Energy Technology Data Exchange (ETDEWEB)

    Hirata, Sawako Horai; Hayase, Daisuke; Eguchi, Akifumi; Itai, Takaaki; Nomiyama, Kei; Isobe, Tomohiko; Agusa, Tetsuro [Center for Marine Environmental Studies (CMES), Ehime University, 2-5 Bunkyo-cho, Matsuyama 790-8577 (Japan); Ishikawa, Toshiyuki [Department of Environmental Education, Faculty of Education, Shiga University, 2-5-1 Hiratsu, Otsu, Shiga 520-0862 (Japan); Kumagai, Michio [Lake Biwa Environmental Research Institute, 5-34 Yanagasaki, Otsu, Shiga 520-0022 (Japan); Tanabe, Shinsuke, E-mail: shinsuke@agr.ehime-u.ac.jp [Center for Marine Environmental Studies (CMES), Ehime University, 2-5 Bunkyo-cho, Matsuyama 790-8577 (Japan)

    2011-10-15

    The present study measured the concentrations of 25 elements (Li, Mg, V, Cr, Mn, Co, Ni, Cu, Zn, As, Se, Rb, Sr, Mo, Ag, Cd, In, Sn, Sb, Cs, Ba, Hg, Tl, Pb and Bi) in the whole body of Isaza which is an endemic fish species to Lake Biwa, Japan, and compared the values in the specimens from the mass mortality Isaza (MMI) and normal fresh Isaza (NFI). The mean levels of Mn and total As (T-As) were relatively higher in MMI than in NFI. In the T-As, highly toxic inorganic As was detected in MMI. Moreover we found Mn and As concentrations in surface sediment were extremely high and temporally increased. From all these results, we could infer that the dissolution of Mn and As from surface sediment of Lake Biwa might have been one of the cause for the mass mortality of Isaza. - Highlights: > Mn and As levels were significantly higher in MMI than in NFI. > The number of chemical species of As detected from MMI was less than that from NFI. > Mn and As levels were highest in surface sediment, and sharply decreased with depth. > Mn and As levels in surface sediment temporally increased. - As and Mn levels in dead Isaza caused by mass mortality.

  3. Electronic Phase Separation in Pr sub 1 sub x (Ca, Sr) sub x MnO sub 3 subdelta and Tunneling Magnetoresistance in Sr sub 2 FeMoO sub 6

    CERN Document Server

    Niebieskikwiat, D G

    2003-01-01

    In this work, we approach two aspects of the physics of magnetic perovskites presenting colossal magnetoresistance (CMR). Firstly, we go deeply into the phase separation (PS) between the ferromagnetic (FM) metallic state and the antiferro-magnetic (AFM) charge ordered (CO) insulating state, in manganites of the type Pr sub 1 sub x (Ca,Sr) sub x MnO sub 3 subdelta. Secondly, and more briefly, we analyze the problem of the influence of the grain boundary insulating barriers on the tunneling magnetoresistance in the Sr sub 2 FeMoO sub 6 double perovskite.The use of different measurement techniques allowed us to make a complete characterization of the PS state in the compounds Pr sub 0.65Ca sub 0 sub . sub 3 sub 5 sub - sub y Sr sub y MnO sub 3 for 0 ) keeping constant the carrier concentration (x = 0.35). This material presents an evolution from a CO insulating phase for small (y =0), towards the FM metallic phase for large (y = 0.20). In t

  4. Study on the Heat Treatment Process for the Steel Tube of Grade Q125 with 30CrMnMo%30CrMnMo钢调质Q125钢级套管的工艺研究

    Institute of Scientific and Technical Information of China (English)

    马爱清; 郭兆成; 贺景春

    2009-01-01

    文章采用包钢现有钢种30CrMnMo进行了Q125钢级石油套管的热处理工艺研究.结果表明:该钢在900±10℃保温40-50 min水冷,6304±10℃回火70~80 min后有较好的强度和韧性,力学性能符合 API SPEC 5CT对Q125套管的性能要求.

  5. EFFECT OF HEAT TREATMENT ON MECHANICAL PROPERTIES OF STEEL 25CrMnMo%热处理对25CrMnMo钢组织和性能的影响

    Institute of Scientific and Technical Information of China (English)

    徐天兵

    2004-01-01

    研究了热处理对新型热轧调质无缝油管用25CrMnMo钢性能的影响.结果表明:该钢在920℃保温30 min水冷,650℃回火70 min后有较好的强度和韧性.通过选择不同的调质工艺可以满足API 5CT标准中N80Q和P110等高钢级油管的性能要求.

  6. Chemical thermodynamics of Hg1201 and Hg1223 phases

    Science.gov (United States)

    Tsuchiya, Tetsuo; Fueki, Kazuo; Koyama, Tadashi

    1998-03-01

    The decomposition equilibrium of Hg1201 and Hg1223 was studied using a thermomicrobalance. A thermodynamic diagram representing the stability domains of Hg1201 and Hg1223 was constructed. Using the diagram, it was shown that Hg1201 is metastable at 800°C and that Hg1223 is stable at 660°C due to the formation of an atmosphere of mercury vapor and oxygen formed by the decomposition of excess HgO. Chemical analysis revealed that the valence of Hg is +2 regardless of the oxygen content. The dependence of Tc on the oxygen content was also studied.

  7. Measurement of the direct CP -violating parameter ACP in the decay D<mo>+ stretchy='false'>→mo>K<mo>-mo>π<mo>+mo>π+>

    Energy Technology Data Exchange (ETDEWEB)

    Abazov, V. M.; Abbott, B.; Acharya, B. S.; Adams, M.; Adams, T.; Agnew, J. P.; Alexeev, G. D.; Alkhazov, G.; Alton, A.; Askew, A.; Atkins, S.; Augsten, K.; Avila, C.; Badaud, F.; Bagby, L.; Baldin, B.; Bandurin, D. V.; Banerjee, S.; Barberis, E.; Baringer, P.; Bartlett, J. F.; Bassler, U.; Bazterra, V.; Bean, A.; Begalli, M.; Bellantoni, L.; Beri, S. B.; Bernardi, G.; Bernhard, R.; Bertram, I.; Besançon, M.; Beuselinck, R.; Bhat, P. C.; Bhatia, S.; Bhatnagar, V.; Blazey, G.; Blessing, S.; Bloom, K.; Boehnlein, A.; Boline, D.; Boos, E. E.; Borissov, G.; Borysova, M.; Brandt, A.; Brandt, O.; Brock, R.; Bross, A.; Brown, D.; Bu, X. B.; Buehler, M.; Buescher, V.; Bunichev, V.; Burdin, S.; Buszello, C. P.; Camacho-Pérez, E.; Casey, B. C. K.; Castilla-Valdez, H.; Caughron, S.; Chakrabarti, S.; Chan, K. M.; Chandra, A.; Chapon, E.; Chen, G.; Cho, S. W.; Choi, S.; Choudhary, B.; Cihangir, S.; Claes, D.; Clutter, J.; Cooke, M.; Cooper, W. E.; Corcoran, M.; Couderc, F.; Cousinou, M. -C.; Cutts, D.; Das, A.; Davies, G.; de Jong, S. J.; De La Cruz-Burelo, E.; Déliot, F.; Demina, R.; Denisov, D.; Denisov, S. P.; Desai, S.; Deterre, C.; DeVaughan, K.; Diehl, H. T.; Diesburg, M.; Ding, P. F.; Dominguez, A.; Dubey, A.; Dudko, L. V.; Duperrin, A.; Dutt, S.; Eads, M.; Edmunds, D.; Ellison, J.; Elvira, V. D.; Enari, Y.; Evans, H.; Evdokimov, V. N.; Fauré, A.; Feng, L.; Ferbel, T.; Fiedler, F.; Filthaut, F.; Fisher, W.; Fisk, H. E.; Fortner, M.; Fox, H.; Fuess, S.; Garbincius, P. H.; Garcia-Bellido, A.; García-González, J. A.; Gavrilov, V.; Geng, W.; Gerber, C. E.; Gershtein, Y.; Ginther, G.; Gogota, O.; Golovanov, G.; Grannis, P. D.; Greder, S.; Greenlee, H.; Grenier, G.; Gris, Ph.; Grivaz, J. -F.; Grohsjean, A.; Grünendahl, S.; Grünewald, M. W.; Guillemin, T.; Gutierrez, G.; Gutierrez, P.; Haley, J.; Han, L.; Harder, K.; Harel, A.; Hauptman, J. M.; Hays, J.; Head, T.; Hebbeker, T.; Hedin, D.; Hegab, H.; Heinson, A. P.; Heintz, U.; Hensel, C.; Heredia-De La Cruz, I.; Herner, K.; Hesketh, G.; Hildreth, M. D.; Hirosky, R.; Hoang, T.; Hobbs, J. D.; Hoeneisen, B.; Hogan, J.; Hohlfeld, M.; Holzbauer, J. L.; Howley, I.; Hubacek, Z.; Hynek, V.; Iashvili, I.; Ilchenko, Y.; Illingworth, R.; Ito, A. S.; Jabeen, S.; Jaffré, M.; Jayasinghe, A.; Jeong, M. S.; Jesik, R.; Jiang, P.; Johns, K.; Johnson, E.; Johnson, M.; Jonckheere, A.; Jonsson, P.; Joshi, J.; Jung, A. W.; Juste, A.; Kajfasz, E.; Karmanov, D.; Katsanos, I.; Kaur, M.; Kehoe, R.; Kermiche, S.; Khalatyan, N.; Khanov, A.; Kharchilava, A.; Kharzheev, Y. N.; Kiselevich, I.; Kohli, J. M.; Kozelov, A. V.; Kraus, J.; Kumar, A.; Kupco, A.; Kurča, T.; Kuzmin, V. A.; Lammers, S.; Lebrun, P.; Lee, H. S.; Lee, S. W.; Lee, W. M.; Lei, X.; Lellouch, J.; Li, D.; Li, H.; Li, L.; Li, Q. Z.; Lim, J. K.; Lincoln, D.; Linnemann, J.; Lipaev, V. V.; Lipton, R.; Liu, H.; Liu, Y.; Lobodenko, A.; Lokajicek, M.; Lopes de Sa, R.; Luna-Garcia, R.; Lyon, A. L.; Maciel, A. K. A.; Madar, R.; Magaña-Villalba, R.; Malik, S.; Malyshev, V. L.; Mansour, J.; Martínez-Ortega, J.; McCarthy, R.; McGivern, C. L.; Meijer, M. M.; Melnitchouk, A.; Menezes, D.; Mercadante, P. G.; Merkin, M.; Meyer, A.; Meyer, J.; Miconi, F.; Mondal, N. K.; Mulhearn, M.; Nagy, E.; Narain, M.; Nayyar, R.; Neal, H. A.; Negret, J. P.; Neustroev, P.; Nguyen, H. T.; Nunnemann, T.; Orduna, J.; Osman, N.; Osta, J.; Pal, A.; Parashar, N.; Parihar, V.; Park, S. K.; Partridge, R.; Parua, N.; Patwa, A.; Penning, B.; Perfilov, M.; Peters, Y.; Petridis, K.; Petrillo, G.; Pétroff, P.; Pleier, M. -A.; Podstavkov, V. M.; Popov, A. V.; Prewitt, M.; Price, D.; Prokopenko, N.; Qian, J.; Quadt, A.; Quinn, B.; Ratoff, P. N.; Razumov, I.; Ripp-Baudot, I.; Rizatdinova, F.; Rominsky, M.; Ross, A.; Royon, C.; Rubinov, P.; Ruchti, R.; Sajot, G.; Sánchez-Hernández, A.; Sanders, M. P.; Santos, A. S.; Savage, G.; Savitskyi, M.; Sawyer, L.; Scanlon, T.; Schamberger, R. D.; Scheglov, Y.; Schellman, H.; Schwanenberger, C.; Schwienhorst, R.; Sekaric, J.; Severini, H.; Shabalina, E.; Shary, V.; Shaw, S.; Shchukin, A. A.; Simak, V.; Skubic, P.; Slattery, P.; Smirnov, D.; Snow, G. R.; Snow, J.; Snyder, S.; Söldner-Rembold, S.; Sonnenschein, L.; Soustruznik, K.; Stark, J.; Stoyanova, D. A.; Strauss, M.; Suter, L.; Svoisky, P.; Titov, M.; Tokmenin, V. V.; Tsai, Y. -T.; Tsybychev, D.; Tuchming, B.; Tully, C.; Uvarov, L.; Uvarov, S.; Uzunyan, S.; Van Kooten, R.; van Leeuwen, W. M.; Varelas, N.; Varnes, E. W.; Vasilyev, I. A.; Verkheev, A. Y.; Vertogradov, L. S.; Verzocchi, M.; Vesterinen, M.; Vilanova, D.; Vokac, P.; Wahl, H. D.; Wang, M. H. L. S.; Warchol, J.; Watts, G.; Wayne, M.; Weichert, J.; Welty-Rieger, L.; Williams, M. R. J.; Wilson, G. W.; Wobisch, M.; Wood, D. R.; Wyatt, T. R.; Xie, Y.; Yamada, R.; Yang, S.; Yasuda, T.; Yatsunenko, Y. A.; Ye, W.; Ye, Z.; Yin, H.; Yip, K.; Youn, S. W.; Yu, J. M.; Zennamo, J.; Zhao, T. G.; Zhou, B.; Zhu, J.; Zielinski, M.; Zieminska, D.; Zivkovic, L.

    2014-12-01

    We measure the direct CP-violating parameter ACP for the decay of the charged charm meson, Dmo>+ stretchy="false">→mo>Kmo>-mo>πmo>+mo>πmo>+> (and charge conjugate), using the full mn>10.4mn> fbmo>->1mn> sample of ppmo accent="true" stretchy="false">¯mo> collisions at smo>=>1.96mn> TeV collected by the D0 detector at the Fermilab Tevatron collider. We extract the raw reconstructed charge asymmetry by fitting the invariant mass distributions for the sum and difference of charge-specific samples. This quantity is then corrected for detector-related asymmetries using data-driven methods and for possible physics asymmetries (from Bmo stretchy="false">→mo

  8. Measurement of the direct CP -violating parameter ACP in the decay D<mo>+ stretchy='false'>→mo>K<mo>-mo>π<mo>+mo>π+>

    Energy Technology Data Exchange (ETDEWEB)

    Abazov, V. M.; Abbott, B.; Acharya, B. S.; Adams, M.; Adams, T.; Agnew, J. P.; Alexeev, G. D.; Alkhazov, G.; Alton, A.; Askew, A.; Atkins, S.; Augsten, K.; Avila, C.; Badaud, F.; Bagby, L.; Baldin, B.; Bandurin, D. V.; Banerjee, S.; Barberis, E.; Baringer, P.; Bartlett, J. F.; Bassler, U.; Bazterra, V.; Bean, A.; Begalli, M.; Bellantoni, L.; Beri, S. B.; Bernardi, G.; Bernhard, R.; Bertram, I.; Besançon, M.; Beuselinck, R.; Bhat, P. C.; Bhatia, S.; Bhatnagar, V.; Blazey, G.; Blessing, S.; Bloom, K.; Boehnlein, A.; Boline, D.; Boos, E. E.; Borissov, G.; Borysova, M.; Brandt, A.; Brandt, O.; Brock, R.; Bross, A.; Brown, D.; Bu, X. B.; Buehler, M.; Buescher, V.; Bunichev, V.; Burdin, S.; Buszello, C. P.; Camacho-Pérez, E.; Casey, B. C. K.; Castilla-Valdez, H.; Caughron, S.; Chakrabarti, S.; Chan, K. M.; Chandra, A.; Chapon, E.; Chen, G.; Cho, S. W.; Choi, S.; Choudhary, B.; Cihangir, S.; Claes, D.; Clutter, J.; Cooke, M.; Cooper, W. E.; Corcoran, M.; Couderc, F.; Cousinou, M. -C.; Cutts, D.; Das, A.; Davies, G.; de Jong, S. J.; De La Cruz-Burelo, E.; Déliot, F.; Demina, R.; Denisov, D.; Denisov, S. P.; Desai, S.; Deterre, C.; DeVaughan, K.; Diehl, H. T.; Diesburg, M.; Ding, P. F.; Dominguez, A.; Dubey, A.; Dudko, L. V.; Duperrin, A.; Dutt, S.; Eads, M.; Edmunds, D.; Ellison, J.; Elvira, V. D.; Enari, Y.; Evans, H.; Evdokimov, V. N.; Fauré, A.; Feng, L.; Ferbel, T.; Fiedler, F.; Filthaut, F.; Fisher, W.; Fisk, H. E.; Fortner, M.; Fox, H.; Fuess, S.; Garbincius, P. H.; Garcia-Bellido, A.; García-González, J. A.; Gavrilov, V.; Geng, W.; Gerber, C. E.; Gershtein, Y.; Ginther, G.; Gogota, O.; Golovanov, G.; Grannis, P. D.; Greder, S.; Greenlee, H.; Grenier, G.; Gris, Ph.; Grivaz, J. -F.; Grohsjean, A.; Grünendahl, S.; Grünewald, M. W.; Guillemin, T.; Gutierrez, G.; Gutierrez, P.; Haley, J.; Han, L.; Harder, K.; Harel, A.; Hauptman, J. M.; Hays, J.; Head, T.; Hebbeker, T.; Hedin, D.; Hegab, H.; Heinson, A. P.; Heintz, U.; Hensel, C.; Heredia-De La Cruz, I.; Herner, K.; Hesketh, G.; Hildreth, M. D.; Hirosky, R.; Hoang, T.; Hobbs, J. D.; Hoeneisen, B.; Hogan, J.; Hohlfeld, M.; Holzbauer, J. L.; Howley, I.; Hubacek, Z.; Hynek, V.; Iashvili, I.; Ilchenko, Y.; Illingworth, R.; Ito, A. S.; Jabeen, S.; Jaffré, M.; Jayasinghe, A.; Jeong, M. S.; Jesik, R.; Jiang, P.; Johns, K.; Johnson, E.; Johnson, M.; Jonckheere, A.; Jonsson, P.; Joshi, J.; Jung, A. W.; Juste, A.; Kajfasz, E.; Karmanov, D.; Katsanos, I.; Kaur, M.; Kehoe, R.; Kermiche, S.; Khalatyan, N.; Khanov, A.; Kharchilava, A.; Kharzheev, Y. N.; Kiselevich, I.; Kohli, J. M.; Kozelov, A. V.; Kraus, J.; Kumar, A.; Kupco, A.; Kurča, T.; Kuzmin, V. A.; Lammers, S.; Lebrun, P.; Lee, H. S.; Lee, S. W.; Lee, W. M.; Lei, X.; Lellouch, J.; Li, D.; Li, H.; Li, L.; Li, Q. Z.; Lim, J. K.; Lincoln, D.; Linnemann, J.; Lipaev, V. V.; Lipton, R.; Liu, H.; Liu, Y.; Lobodenko, A.; Lokajicek, M.; Lopes de Sa, R.; Luna-Garcia, R.; Lyon, A. L.; Maciel, A. K. A.; Madar, R.; Magaña-Villalba, R.; Malik, S.; Malyshev, V. L.; Mansour, J.; Martínez-Ortega, J.; McCarthy, R.; McGivern, C. L.; Meijer, M. M.; Melnitchouk, A.; Menezes, D.; Mercadante, P. G.; Merkin, M.; Meyer, A.; Meyer, J.; Miconi, F.; Mondal, N. K.; Mulhearn, M.; Nagy, E.; Narain, M.; Nayyar, R.; Neal, H. A.; Negret, J. P.; Neustroev, P.; Nguyen, H. T.; Nunnemann, T.; Orduna, J.; Osman, N.; Osta, J.; Pal, A.; Parashar, N.; Parihar, V.; Park, S. K.; Partridge, R.; Parua, N.; Patwa, A.; Penning, B.; Perfilov, M.; Peters, Y.; Petridis, K.; Petrillo, G.; Pétroff, P.; Pleier, M. -A.; Podstavkov, V. M.; Popov, A. V.; Prewitt, M.; Price, D.; Prokopenko, N.; Qian, J.; Quadt, A.; Quinn, B.; Ratoff, P. N.; Razumov, I.; Ripp-Baudot, I.; Rizatdinova, F.; Rominsky, M.; Ross, A.; Royon, C.; Rubinov, P.; Ruchti, R.; Sajot, G.; Sánchez-Hernández, A.; Sanders, M. P.; Santos, A. S.; Savage, G.; Savitskyi, M.; Sawyer, L.; Scanlon, T.; Schamberger, R. D.; Scheglov, Y.; Schellman, H.; Schwanenberger, C.; Schwienhorst, R.; Sekaric, J.; Severini, H.; Shabalina, E.; Shary, V.; Shaw, S.; Shchukin, A. A.; Simak, V.; Skubic, P.; Slattery, P.; Smirnov, D.; Snow, G. R.; Snow, J.; Snyder, S.; Söldner-Rembold, S.; Sonnenschein, L.; Soustruznik, K.; Stark, J.; Stoyanova, D. A.; Strauss, M.; Suter, L.; Svoisky, P.; Titov, M.; Tokmenin, V. V.; Tsai, Y. -T.; Tsybychev, D.; Tuchming, B.; Tully, C.; Uvarov, L.; Uvarov, S.; Uzunyan, S.; Van Kooten, R.; van Leeuwen, W. M.; Varelas, N.; Varnes, E. W.; Vasilyev, I. A.; Verkheev, A. Y.; Vertogradov, L. S.; Verzocchi, M.; Vesterinen, M.; Vilanova, D.; Vokac, P.; Wahl, H. D.; Wang, M. H. L. S.; Warchol, J.; Watts, G.; Wayne, M.; Weichert, J.; Welty-Rieger, L.; Williams, M. R. J.; Wilson, G. W.; Wobisch, M.; Wood, D. R.; Wyatt, T. R.; Xie, Y.; Yamada, R.; Yang, S.; Yasuda, T.; Yatsunenko, Y. A.; Ye, W.; Ye, Z.

    2014-12-01

    We measure the direct CP-violating parameter ACP for the decay of the charged charm meson, Dmo>+ stretchy="false">→mo>Kmo>-mo>πmo>+mo>πmo>+> (and charge conjugate), using the full mn>10.4mn> fbmo>->1mn> sample of ppmo accent="true" stretchy="false">¯mo> collisions at smo>=>1.96mn> TeV collected by the D0 detector at the Fermilab Tevatron collider. We extract the raw reconstructed charge asymmetry by fitting the invariant mass distributions for the sum and difference of charge-specific samples. This quantity is then corrected for detector-related asymmetries using data-driven methods and for possible physics asymmetries (from Bmo stretchy="false">→mo

  9. Spectral and thermodynamic properties of Ag(I), Au(III), Cd(II), Co(II), Fe(III), Hg(II), Mn(II), Ni(II), Pb(II), U(IV), and Zn(II) binding by methanobactin from Methylosinus trichosporium OB3b.

    Science.gov (United States)

    Choi, Dong W; Do, Young S; Zea, Corbin J; McEllistrem, Marcus T; Lee, Sung-W; Semrau, Jeremy D; Pohl, Nicola L; Kisting, Clint J; Scardino, Lori L; Hartsel, Scott C; Boyd, Eric S; Geesey, Gill G; Riedel, Theran P; Shafe, Peter H; Kranski, Kim A; Tritsch, John R; Antholine, William E; DiSpirito, Alan A

    2006-12-01

    Methanobactin (mb) is a novel chromopeptide that appears to function as the extracellular component of a copper acquisition system in methanotrophic bacteria. To examine this potential physiological role, and to distinguish it from iron binding siderophores, the spectral (UV-visible absorption, circular dichroism, fluorescence, and X-ray photoelectron) and thermodynamic properties of metal binding by mb were examined. In the absence of Cu(II) or Cu(I), mb will bind Ag(I), Au(III), Co(II), Cd(II), Fe(III), Hg(II), Mn(II), Ni(II), Pb(II), U(VI), or Zn(II), but not Ba(II), Ca(II), La(II), Mg(II), and Sr(II). The results suggest metals such as Ag(I), Au(III), Hg(II), Pb(II) and possibly U(VI) are bound by a mechanism similar to Cu, whereas the coordination of Co(II), Cd(II), Fe(III), Mn(II), Ni(II) and Zn(II) by mb differs from Cu(II). Consistent with its role as a copper-binding compound or chalkophore, the binding constants of all the metals examined were less than those observed with Cu(II) and copper displaced other metals except Ag(I) and Au(III) bound to mb. However, the binding of different metals by mb suggests that methanotrophic activity also may play a role in either the solubilization or immobilization of many metals in situ.

  10. Controlled reduction of LaFe xMn yMo zO3/Al2O3 composites to produce highly dispersed and stable Fe0 catalysts: a Mössbauer investigation

    Directory of Open Access Journals (Sweden)

    Juliana Cristina Tristão

    2008-06-01

    Full Text Available In this work, controlled reduction of perovskites supported on Al2O3 was used to prepare thermally stable nanodispersed iron catalysts based on Fe0/La2O3/Al2O3. The perovskites composites LaFe0.90Mn0.08Mo0.02O3(25, 33 and 50 wt (% /Al2O3 and LaFe0.90Mn0.1O3(25 wt (% /Al2O3 were prepared and characterized by XRD, BET, TPR, SEM and Mössbauer spectroscopy. XRD for unsupported perovskite showed the formation of a single phase perovskite structure. The Mössbauer spectra of the perovskites were fitted with hyperfine field distribution model for the perovskite. Supported perovskites on Al2O3 showed a decrease of the hyperfine field in respect to unsupported perovskite, due to decrease of particle size and dispersion of the Fe3+ specimens on the support. Also showed broaden lines and relaxation effects due to the small particle size. To produce the Fe0 catalyst, the composite perovskite(25%/Al2O3 was reduced with H2 at 900, 1000 and 1100 °C for 1 hour. XRD data indicated the formation of Fe0 catalyst with particles sizes of ca. 35 nm. The Mössbauer spectrum showed the formation of metallic iron and doublets corresponding to species of octahedric Fe2+ and Fe3+ sites dispersed on Al2O3. These catalysts showed improved stability towards sintering even upon treatment at 1000 and 1100 °C under H2.

  11. Welding and corrosion resistance of the new nitrogen alloyed steel X2 CrNiMnMoN241764. Caracteristicas de soldadura y resistencia a la corrosion de nuevo acero X2 CrNiMnMoN 241764 aleado con nitrogeno

    Energy Technology Data Exchange (ETDEWEB)

    Arit, N.; Henser, H.; GroB, V.

    1994-01-01

    Remanit 4565 S is a new developed nitrogen alloyed austenitic stainless steel. Characteristic features are: improved strength and toughness, delayed precipitation of carbides and intermetallic phases, improved corrosion resistance. Welding fabrication is possible without the risk of pore formation. TIG-welded joints are as resistant as the base metal, using filler metal SG-NiCr 20 Mo 15 (Thermanit Nimo C) respectively SG-NiCr 28 Mo(Thermanit 30/40 E) according to the area of application. (Author) 8 refs.

  12. Study of the properties of flux cored wire of Fe-C-Si-Mn-Cr-Mo-Ni-V-Co system for the strengthening of nodes and parts of equipment used in the mineral mining

    Science.gov (United States)

    Gusev, A. I.; Kozyrev, N. A.; Usoltsev, A. A.; Kryukov, R. E.; Osetkovsky, I. V.

    2017-09-01

    The effect of the introduction of vanadium and cobalt into the charge of the powder surfacing wire of Fe-C-Si-Mn-Cr-Mo-Ni system is studied. In the laboratory conditions, the samples of flux cored wires were produced. The surfacing made by the prepared wire was produced under the flux AN-26C, on the plates of steel St3 in 6 layers with the help of ASAW-1250 welding tractor. Reduction of carbon content in the deposited layer to 0.19-0.2% with simultaneous change in the content of chromium, nickel, molybdenum and other elements present in it contributes to the enlargement of the martensite needles and the increase in the size of the former austenite grain. The obtained dependences of hardness of the deposited layer and its wear resistance on the mass fraction of elements, included in the composition of powder wires of the proposed system, can be used to predict the hardness of the welded layer and its wear resistance under different operating conditions for mining equipment and coal mining equipment.

  13. Chemical synthesis and properties of La1.9Ba0.1Mo1.9Mn0.1O9 as electrolyte for IT-SOFCs

    Institute of Scientific and Technical Information of China (English)

    田长安; 尹奇异; 谢劲松; 阳杰; 孙虹; 季必发; 鲍魏涛

    2014-01-01

    The highly phase-pure electrolyte materials with composition La1.9Ba0.1Mo1.9Mn0.1O9 (LBMMO) was prepared by the sol-gel auto-combustion method for intermediate-temperature solid oxide fuel cells (IT-SOFCs). The details of gel’s auto-combustion, phase evolution, sintering, thermal expansion and electrochemical performance of LBMMO were investigated by means of thermo-gravimetry (TG), X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron spectroscopy (TEM), thermal expansion curve (TEC) and complex impedance spectra. The results showed that the highly phase-pure electrolyte LBMMO could be obtained after calcining at 600 °C. The sample sintered at 900 °C for 4 h in air exhibited a better sinterability, and the relative density of LBMMO was higher than 96%. The electrical conductivities of the sample were 6.7×10-3 and 25.9×10-3 S/cm at 700 and 800 °C in air, respectively. Results also showed that LBMMO had moderate thermal expansion (α=16.3×10-6 K-1, between room temperature and 800 °C) and an electrical activation energy equal to 1.32 eV).

  14. New series of triple molybdates AgA{sub 3}R(MoO{sub 4}){sub 5} (A=Mg, R=Cr, Fe; A=Mn, R=Al, Cr, Fe, Sc, In) with framework structures and mobile silver ion sublattices

    Energy Technology Data Exchange (ETDEWEB)

    Kotova, Irina Yu. [Baikal Institute of Nature Management, Siberian Branch, Russian Academy of Sciences, Sakh’yanova St. 6, Ulan-Ude 670047, Buryat Republic (Russian Federation); Buryat State University, Smolin St. 24a, Ulan-Ude 670000, Buryat Republic (Russian Federation); Solodovnikov, Sergey F. [Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences, Acad. Lavrentiev Ave. 3, Novosibirsk 630090 (Russian Federation); Novosibirsk State University, Pirogov St. 2, Novosibirsk 630090 (Russian Federation); Solodovnikova, Zoya A. [Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences, Acad. Lavrentiev Ave. 3, Novosibirsk 630090 (Russian Federation); Belov, Dmitry A.; Stefanovich, Sergey Yu. [Lomonosov Moscow State University, Leninskie Gory 1, Moscow 119991 (Russian Federation); Savina, Aleksandra A., E-mail: alex551112@mail.ru [Baikal Institute of Nature Management, Siberian Branch, Russian Academy of Sciences, Sakh’yanova St. 6, Ulan-Ude 670047, Buryat Republic (Russian Federation); Buryat State University, Smolin St. 24a, Ulan-Ude 670000, Buryat Republic (Russian Federation); Khaikina, Elena G. [Baikal Institute of Nature Management, Siberian Branch, Russian Academy of Sciences, Sakh’yanova St. 6, Ulan-Ude 670047, Buryat Republic (Russian Federation); Buryat State University, Smolin St. 24a, Ulan-Ude 670000, Buryat Republic (Russian Federation)

    2016-06-15

    Triple molybdates AgA{sub 3}R(MoO{sub 4}){sub 5} (A=Mg, R=Cr, Fe; A=Mn, R=Al, Cr, Fe, Sc, In) of the NaMg{sub 3}In(MoO{sub 4}){sub 5} type were synthesized and single crystals of AgMg{sub 3}R(MoO{sub 4}){sub 5} (R=Cr, Fe) were grown. In their structures, the MoO{sub 4} tetrahedra, pairs and trimers of edge-shared (Mg, R)O{sub 6} octahedra are connected by common vertices to form a 3D framework. Large framework cavities involve Ag{sup +} cations disordered on three nearby positions with CN=3+1 or 4+1. Alternating (Mg, R)O{sub 6} octahedra and MoO{sub 4} tetrahedra in the framework form quadrangular windows penetrable for Ag{sup +} at elevated temperatures. Above 653–673 K, the newly obtained molybdates demonstrate abrupt reduction of the activation energy to 0.4–0.6 eV. At 773 K, AgMg{sub 3}Al(MoO{sub 4}){sub 5} shows electric conductivity 2.5·10{sup −2} S/cm and E{sub a}=0.39 eV compatible with characteristics of the best ionic conductors of the NASICON type. - Graphical abstract: Triple molybdates AgA{sub 3}R(MoO{sub 4}){sub 5} (A=Mg, R=Cr, Fe; A=Mn, R=Al, Cr, Fe, Sc, In) of the NaMg{sub 3}In(MoO{sub 4}){sub 5} type were synthesized, AgMg{sub 3}R(MoO{sub 4}){sub 5} (R=Cr, Fe) were structurally characterized, ion-conductive properties of AgMg{sub 3}Al(MoO{sub 4}){sub 5} were measured. Display Omitted - Highlights: • Triple molybdates AgA{sub 3}R(MoO{sub 4}){sub 5} (A=Mg, R=Cr, Fe; A=Mn, R=Al, Cr, Fe, Sc, In) of the NaMg{sub 3}In(MoO{sub 4}){sub 5} type were synthesized. • Single crystals of AgMg{sub 3}R(MoO{sub 4}){sub 5} (R=Cr, Fe) were grown and their crystal structures were determined. • Disordering Ag{sup +} ions and penetrable framework structures of AgMg{sub 3}R(MoO{sub 4}){sub 5} (R=Cr, Fe) suggest 2D-character of silver-ion mobility. • Measured ion-conductive properties of AgMg{sub 3}Al(MoO{sub 4}){sub 5} are compatible with characteristics of the best ionic conductors of the NASICON type.

  15. Density functional investigation of metal-metal interactions in mixed-valence d2d3 (Cr, Mo, W) and d3d4 (Mn, Tc, Re) face-shared [M2Cl9]2- systems.

    Science.gov (United States)

    Cavigliasso, Germán; Comba, Peter; Stranger, Robert

    2004-10-18

    The molecular and electronic structures of mixed-valence face-shared (Cr, Mo, W) d(2)d(3) and (Mn, Tc, Re) d(3)d(4) [M(2)Cl(9)](2-) dimers have been calculated by density functional methods in order to investigate metal-metal bonding in this series. The electronic structures of these systems have been analyzed using potential energy curves for the broken-symmetry and other spin states arising from the d(2)d(3) and d(3)d(4) coupling modes. In (d(2)d(3)) [Mo(2)Cl(9)](2-) and [W(2)Cl(9)](2-), the global minimum has been found to be a spin-doublet state characterized by delocalization of the metal-based electrons in a multiple metal-metal bond (with a formal bond order of 2.5). In contrast, weak coupling between the metal centers and electron localization are favored in (d(2)d(3)) [Cr(2)Cl(9)](2-), the global minimum for this species being a ferromagnetic S = 5/2 state with a relatively long Cr-Cr separation. The (d(3)d(4)) [Re(2)Cl(9)](2-) system also exhibits a global minimum corresponding to a metal-metal bonded spin-doublet state with a formal bond order of 2.5, reflecting the electron-hole equivalence between d(2)d(3) and d(3)d(4) configurations. Double minima behavior is predicted for (d(3)d(4)) [Tc(2)Cl(9)](2-) and [Mn(2)Cl(9)](2-) due to two energetically close low-lying states (these being S = 3/2 and S = 5/2 states for the former, and S = 5/2 and S = 7/2 states for the latter). A comparison of computational results for the d(2)d(2), d(2)d(3), and d(3)d(3) [W(2)Cl(9)](z-) series and the d(3)d(3), d(3)d(4), and d(4)d(4) [Re(2)Cl(9)](z-) series indicates that the observed trends in metal-metal distances can only be rationalized if changes in both the strength of sigma bonding and metal-metal bond order are taken into consideration. These two factors act conjointly in the W series but in opposition to one another in the Re series. In the case of the [Cr(2)Cl(9)](z-) and [Mn(2)Cl(9)](z-) dimers, the metal-metal bond lengths are significantly shorter for mixed

  16. New series of triple molybdates AgA3R(MoO4)5 (A=Mg, R=Cr, Fe; A=Mn, R=Al, Cr, Fe, Sc, In) with framework structures and mobile silver ion sublattices

    Science.gov (United States)

    Kotova, Irina Yu.; Solodovnikov, Sergey F.; Solodovnikova, Zoya A.; Belov, Dmitry A.; Stefanovich, Sergey Yu.; Savina, Aleksandra A.; Khaikina, Elena G.

    2016-06-01

    Triple molybdates AgA3R(MoO4)5 (A=Mg, R=Cr, Fe; A=Mn, R=Al, Cr, Fe, Sc, In) of the NaMg3In(MoO4)5 type were synthesized and single crystals of AgMg3R(MoO4)5 (R=Cr, Fe) were grown. In their structures, the MoO4 tetrahedra, pairs and trimers of edge-shared (Mg, R)O6 octahedra are connected by common vertices to form a 3D framework. Large framework cavities involve Ag+ cations disordered on three nearby positions with CN=3+1 or 4+1. Alternating (Mg, R)O6 octahedra and MoO4 tetrahedra in the framework form quadrangular windows penetrable for Ag+ at elevated temperatures. Above 653-673 K, the newly obtained molybdates demonstrate abrupt reduction of the activation energy to 0.4-0.6 eV. At 773 K, AgMg3Al(MoO4)5 shows electric conductivity 2.5·10-2 S/cm and Ea=0.39 eV compatible with characteristics of the best ionic conductors of the NASICON type.

  17. Effects of metals doping on the removal of Hg and H2S over ceria

    Science.gov (United States)

    Ling, Lixia; Zhao, Zhongbei; Zhao, Senpeng; Wang, Qiang; Wang, Baojun; Zhang, Riguang; Li, Debao

    2017-05-01

    The effects of Mn and Fe doping into the CeO2(111) surface on the simultaneous removal of Hg and H2S was investigated, a density functional theory calculation with the on-site Coulomb interaction taken into account was adopted. The adsorptions of Hg-containing species on perfect CeO2(111), Mn/CeO2(111) and Fe/CeO2(111) surfaces were studied, the results showed that Mn and Fe dopants facilitated Hg adsorption, and more charge transferred from Hg atom to the metal doped surfaces; HgS preferred to adsorb on the perfect surface with the dissociated mode, while with the molecular mode on Mn/CeO2(111) and Fe/CeO2(111) surfaces. The reaction mechanism show that the dissociated S by H2S can easily react with Hg leading to the formation of HgS on Mn/CeO2(111) and Fe/CeO2(111) surfaces, which is crucial to capture mercury.

  18. Hg-Mask Coronagraph

    Science.gov (United States)

    Bourget, P.; Veiga, C. H.; Vieira Martins, R.; Assus, P.; Colas, F.

    In order to optimize the occulting process of a Lyot coronagraph and to provide a high dynamic range imaging, a new kind of occulting disk has been developed at the National Observatory of Rio de Janeiro. A mercury (Hg) drop glued onto an optical window by molecular cohesion and compressed by a pellicle film is used as the occulting disk. The minimum of the superficial tension potential function provides an optical precision (lambda/100) of the toric free surface of the mercury. This process provides a size control for the adaptation to the seeing conditions and to the apparent diameter of a resolved object, and in the case of adaptive optics, to the Airy diameter fraction needed. The occultation is a three dimensional process near the focal plane on the toric free surface that provides an apodization of the occultation. The Hg-Mask coronagraph has been projected for astrometric observations of faint satellites near to Jovian planets and works since 2000 at the 1.6 m telescope of the Pico dos Dias Observatory (OPD - Brazil).

  19. Stabilization of mercury over Mn-based oxides: Speciation and reactivity by temperature programmed desorption analysis.

    Science.gov (United States)

    Xu, Haomiao; Ma, Yongpeng; Huang, Wenjun; Mei, Jian; Zhao, Songjian; Qu, Zan; Yan, Naiqiang

    2017-01-05

    Mercury temperature-programmed desorption (Hg-TPD) method was employed to clarify mercury species over Mn-based oxides. The elemental mercury (Hg(0)) removal mechanism over MnOx was ascribed to chemical-adsorption. HgO was the primary mercury chemical compound adsorbed on the surface of MnOx. Rare earth element (Ce), main group element (Sn) and transition metal elements (Zr and Fe) were chosen for the modification of MnOx. Hg-TPD results indicated that the binding strength of mercury on these binary oxides followed the order of Sn-MnOxmercury (Hg-O), while Zr-MnOx had a strong bond (HgO). Ce-MnOx and Fe-MnOx had similar bonds compared with pure MnOx. Moreover, the effects of SO2 and NO were investigated based on Hg-TPD analysis. SO2 had a poison effect on Hg(0) removal, and the weak bond of mercury can be easily destroyed by SO2. NO was favorable for Hg(0) removal, and the bond strength of mercury was enhanced.

  20. Atomic displacements in dilute alloys of Cr, Nb and Mo

    CERN Document Server

    Sharma, H

    2002-01-01

    Kanzaki lattice static method is used to calculate the atomic displacements due to substitutional impurities in 3d (Cr) and 4d (Nb, Mo) metals. Wills and Harrison interatomic potential is used to calculate dynamical matrix and the impurity-induced forces up to second nearest neighbors. The calculated atomic displacements for 3d, 4d and 5d impurities in Cr (V, Mn, Fe, Ni, Nb, Mo, Ta and W), Nb (V, Cr, Mn, Fe, Zr, Mo, Ta and W) and Mo (V, Cr, Mn, Fe, Zr, Nb, Ta and W) are tabulated up to 10 NN's. The strain field due to 3d impurities is least in Cr metal while it is larger in Nb and Mo metals. For 4d and 5d impurities the strain is larger in Cr metal than in Nb and Mo hosts. Similar trend is found for relaxation energies also. (author)

  1. Atomic displacements in dilute alloys of Cr, Nb and Mo

    Indian Academy of Sciences (India)

    Hitesh Sharma; S Prakash

    2002-09-01

    Kanzaki lattice static method is used to calculate the atomic displacements due to substitutional impurities in 3d (Cr) and 4d (Nb, Mo) metals. Wills and Harrison interatomic potential is used to calculate dynamical matrix and the impurity-induced forces up to second nearest neighbors. The calculated atomic displacements for 3d, 4d and 5d impurities in Cr (V, Mn, Fe, Ni, Nb, Mo, Ta and W), Nb (V, Cr, Mn, Fe, Zr, Mo, Ta and W) and Mo (V, Cr, Mn, Fe, Zr, Nb, Ta and W) are tabulated up to 10 NN’s. The strain field due to 3d impurities is least in Cr metal while it is larger in Nb and Mo metals. For 4d and 5d impurities the strain is larger in Cr metal than in Nb and Mo hosts. Similar trend is found for relaxation energies also.

  2. Síntese e estudo microestrutural de perovsquitas tipo La0,8Ca0,2MO3 (M: Co e Mn para aplicação em catálise automotiva Synthesis and microstructural study of La0.8Ca0.2MO3 (M: Mn and Co perovskites for automotive catalysis

    Directory of Open Access Journals (Sweden)

    J. P. Ribeiro

    2011-09-01

    Full Text Available Materiais com estrutura perovsquita são potenciais catalisadores para prevenir a emissão de componentes indesejáveis ao meio ambiente. Diferentes métodos têm sido propostos para a síntese desses materiais, visando produzir materiais homogêneos com tamanho nanométrico de partículas. Os compostos La0,8Ca0,2MnO3 e La0,8Ca0,2CoO3 foram preparados pelo método dos precursores poliméricos visando sua utilização como catalisadores automotivos. Este método de síntese foi utilizado porque permite a obtenção de pós homogêneos e fases cristalinas a temperaturas mais baixas que os outros métodos tradicionais de síntese. Os materiais foram calcinados a 700 e 900 ºC por 4 h e caracterizados pelas técnicas de análise térmica, difração de raios X e microscopia eletrônica de varredura. As perovsquitas obtidas são nanométricas, monofásicas e com propriedades adequadas para utilização em catálise automotiva.Materials with perovskite structure are potential catalysts for preventing greenhouse gas emissions to the environment. Several methods have been proposed for the synthesis of these materials in order to produce homogeneous powders with nanometric particle size. In the present work, the La0.8Ca0.2MnO3 and La0.8Ca0.2CoO3 systems were prepared by the polymeric precursor method for application in automotive catalysis. This method was chosen because it allows obtaining homogeneous powders and crystalline phases at lower temperatures. The powders were calcined at 700 and 900 ºC for 4 h and characterized by thermal analysis, X-ray diffraction and scanning electron microscopy techniques. The perovskites are nanometric, single phased and present suitable properties for use in automotive catalysis.

  3. Enhanced pairing of quantum critical metals near d<mo>=>3mn>+>1mn>

    Energy Technology Data Exchange (ETDEWEB)

    Fitzpatrick, A. Liam; Kachru, Shamit; Kaplan, Jared; Raghu, S.; Torroba, Gonzalo; Wang, Huajia

    2015-07-20

    We study the dynamics of a quantum critical boson coupled to a Fermi surface in intermediate energy regimes where the Landau damping of the boson can be parametrically controlled, either via large Fermi velocity or by large- N techniques. We develop a systematic approach to the BCS instability of such systems, including careful treatment of the enhanced log 2 and log 3 singularities which appear already at 1-loop. These singularities arise due to the exchange of a critical boson in the Cooper channel and are absent in Fermi liquid theory. We also treat possible instabilities to charge density wave (CDW) formation, and compare the scales Λ BCS and Λ CDW of the onset of the instabilities in different parametric regimes. We address the question of whether the dressing of the fermions into a non-Fermi liquid via interactions with the order parameter field can happen at energies > Λ BCS , Λ CDW .

  4. Photoproduction of the f<mn>1mn>(>1285mn>)> meson

    Energy Technology Data Exchange (ETDEWEB)

    Dickson, R.; Schumacher, R. A.; Adhikari, K. P.; Akbar, Z.; Amaryan, M. J.; Anefalos Pereira, S.; Badui, R. A.; Ball, J.; Battaglieri, M.; Batourine, V.; Bedlinskiy, I.; Biselli, A.; Boiarinov, S.; Briscoe, W. J.; Burkert, V. D.; Cao, T.; Carman, D. S.; Celentano, A.; Chandavar, S.; Charles, G.; Chetry, T.; Ciullo, G.; Colaneri, L.; Cole, P. L.; Compton, N.; Contalbrigo, M.; Cortes, O.; Crede, V.; D' Angelo, A.; Dashyan, N.; De Vita, R.; De Sanctis, E.; Deur, A.; Djalali, C.; Dugger, M.; Dupre, R.; El Alaoui, A.; El Fassi, L.; Eugenio, P.; Fanchini, E.; Fedotov, G.; Filippi, A.; Fleming, J. A.; Gevorgyan, N.; Ghandilyan, Y.; Gilfoyle, G. P.; Giovanetti, K. L.; Girod, F. X.; Gothe, R. W.; Griffioen, K. A.; Guo, L.; Hafidi, K.; Hakobyan, H.; Hanretty, C.; Harrison, N.; Hattawy, M.; Holtrop, M.; Hicks, K.; Hughes, S. M.; Ilieva, Y.; Ireland, D. G.; Ishkhanov, B. S.; Isupov, E. L.; Jiang, H.; Jo, H. S.; Joosten, S.; Keller, D.; Khachatryan, G.; Khandaker, M.; Kim, A.; Kim, W.; Klein, F. J.; Kubarovsky, V.; Kuleshov, S. V.; Lanza, L.; Lenisa, P.; Livingston, K.; Lu, H. Y.; MacGregor, I. J. D.; Mattione, P.; McKinnon, B.; Meyer, C. A.; Mirazita, M.; Markov, N.; Mokeev, V.; Moriya, K.; Munevar, E.; Murdoch, G.; Nadel-Turonski, P.; Net, L. A.; Ni, A.; Osipenko, M.; Ostrovidov, A. I.; Park, K.; Pasyuk, E.; Phelps, W.; Pisano, S.; Pogorelko, O.; Price, J. W.; Prok, Y.; Puckett, A. J. R.; Raue, B. A.; Ripani, M.; Rizzo, A.; Rosner, G.; Roy, P.; Salgado, C.; Seder, E.; Sharabian, Y. G.; Skorodumina, Iu.; Smith, E. S.; Smith, G. D.; Sober, D.; Sokhan, D.; Sparveris, N.; Stepanyan, S.; Strakovsky, I. I.; Stankovic, I.; Strauch, S.; Sytnik, V.; Taiuti, M.; Ungaro, M.; Voskanyan, H.; Voutier, E.; Walford, N. K.; Watts, D. P.; Weygand, D.; Wood, M. H.; Zachariou, N.; Zana, L.; Zhang, J.; Zonta, I.

    2016-06-01

    The f(1)(1285) meson withmass 1281.0 +/- 0.8MeV/c(2) and width 18.4 +/- 1.4MeV (full width at half maximum) was measured for the first time in photoproduction from a proton target using CLAS at Jefferson Lab. Differential cross sections were obtained via the eta pi(+)pi(-), K+(K) over bar (0) pi(-), and (K-K0)pi(+) decay channels from threshold up to a center-of-mass energy of 2.8 GeV. The mass, width, and an amplitude analysis of the eta pi(+)pi(-) final-state Dalitz distribution are consistent with the axial-vector J(P) = 1(+) f(1)(1285) identity, rather than the pseudoscalar 0(-) eta(1295). The production mechanism is more consistent with s-channel decay of a high-mass N* state and not with t-channel meson exchange. Decays to eta pi pi go dominantly via the intermediate a(0)(+/-) (980)pi(-/+) states, with the branching ratio Gamma [a(0)pi (no (K) over barK)]/Gamma[eta pi pi (all)] = 0.74 +/- 0.09. The branching ratios Gamma (K (K) over bar pi)/Gamma(eta pi pi) = 0.216 +/- 0.033 and Gamma (gamma rho(0))/Gamma(eta pi pi) = 0.047 +/- 0.018 were also obtained. The first is in agreement with previous data for the f(1)(1285), while the latter is lower than the world average.

  5. Photoproduction of the f<mn>1mn>(>1285mn>)> meson

    Energy Technology Data Exchange (ETDEWEB)

    Dickson, Ryan [Carnegie Mellon Univ., Pittsburgh, PA (United States); Schumacher, Reinhard A. [Carnegie Mellon Univ., Pittsburgh, PA (United States); Adhikari, K. P.; Akbar, Z.; Amaryan, M. J.; Anefalos Pereira, S.; Badui, R. A.; Ball, J.; Battaglieri, M.; Batourine, V.; Bedlinskiy, I.; Biselli, A.; Boiarinov, S.; Briscoe, W. J.; Burkert, V. D.; Cao, T.; Carman, D. S.; Celentano, A.; Chandavar, S.; Charles, G.; Chetry, T.; Ciullo, G.; Colaneri, L.; Cole, P. L.; Compton, N.; Contalbrigo, M.; Cortes, O.; Crede, V.; D' Angelo, A.; Dashyan, N.; De Vita, R.; De Sanctis, E.; Deur, A.; Djalali, C.; Dugger, M.; Dupre, R.; El Alaoui, A.; El Fassi, L.; Eugenio, P.; Fanchini, E.; Fedotov, G.; Filippi, A.; Fleming, J. A.; Gevorgyan, N.; Ghandilyan, Y.; Gilfoyle, G. P.; Giovanetti, K. L.; Girod, F. X.; Gothe, R. W.; Griffioen, K. A.; Guo, L.; Hafidi, K.; Hakobyan, H.; Hanretty, C.; Harrison, N.; Hattawy, M.; Holtrop, M.; Hicks, K.; Hughes, S. M.; Ilieva, Y.; Ireland, D. G.; Ishkhanov, B. S.; Isupov, E. L.; Jiang, H.; Jo, H. S.; Joosten, S.; Keller, D.; Khachatryan, G.; Khandaker, M.; Kim, A.; Kim, W.; Klein, F. J.; Kubarovsky, V.; Kuleshov, S. V.; Lanza, L.; Lenisa, P.; Livingston, K.; Lu, H. Y.; MacGregor, I. J. D.; Mattione, P.; McKinnon, B.; Meyer, C. A.; Mirazita, M.; Markov, N.; Mokeev, V.; Moriya, K.; Munevar, E.; Murdoch, G.; Nadel-Turonski, P.; Net, L. A.; Ni, A.; Osipenko, M.; Ostrovidov, A. I.; Park, K.; Pasyuk, E.; Phelps, W.; Pisano, S.; Pogorelko, O.; Price, J. W.; Prok, Y.; Puckett, A. J. R.; Raue, B. A.; Ripani, M.; Rizzo, A.; Rosner, G.; Roy, P.; Salgado, C.; Seder, E.; Sharabian, Y. G.; Skorodumina, Iu.; Smith, E. S.; Smith, G. D.; Sober, D.; Sokhan, D.; Sparveris, N.; Stepanyan, S.; Strakovsky, I. I.; Stankovic, I.; Strauch, S.; Sytnik, V.; Taiuti, M.; Ungaro, M.; Voskanyan, H.; Voutier, E.; Walford, N. K.; Watts, D. P.; Weygand, D.; Wood, M. H.; Zachariou, N.; Zana, L.; Zhang, J.; Zonta, I.

    2016-06-01

    The $f_1(1285)$ meson with mass $1281.0 \\pm 0.8$ MeV/$c^2$ and width $18.4 \\pm 1.4$ MeV (FWHM) was measured for the first time in photoproduction from a proton target using CLAS at Jefferson Lab. Differential cross sections were obtained via the $\\eta\\pi^{+}\\pi^{-}$, $K^+\\bar{K}^0\\pi^-$, and $K^-K^0\\pi^+$ decay channels from threshold up to a center-of-mass energy of 2.8 GeV. The mass, width, and an amplitude analysis of the $\\eta\\pi^{+}\\pi^{-}$ final-state Dalitz distribution are consistent with the axial-vector $J^P=1^+$ $f_1(1285)$ identity, rather than the pseudoscalar $0^-$ $\\eta(1295)$. The production mechanism is more consistent with $s$-channel decay of a high-mass $N^*$ state, and not with $t$-channel meson exchange. Decays to $\\eta\\pi\\pi$ go dominantly via the intermediate $a_0^\\pm(980)\\pi^\\mp$ states, with the branching ratio $\\Gamma(a_0\\pi \\text{ (no} \\bar{K} K\\text{)}) / \\Gamma(\\eta\\pi\\pi \\text{(all)}) = 0.74\\pm0.09$. The branching ratios $\\Gamma(K \\bar{K} \\pi)/\\Gamma(\\eta\\pi\\pi) = 0.216\\pm0.033$ and $\\Gamma(\\gamma\\rho^0)/\\Gamma(\\eta\\pi\\pi) = 0.047\\pm0.018$ were also obtained. The first is in agreement with previous data for the $f_1(1285)$, while the latter is lower than the world average.

  6. In situ DRIFTs investigation of the reaction mechanism over MnO{sub x}-MO{sub y}/Ce{sub 0.75}Zr{sub 0.25}O{sub 2} (M = Fe, Co, Ni, Cu) for the selective catalytic reduction of NO{sub x} with NH{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Hu, Hang; Zha, Kaiwen; Li, Hongrui; Shi, Liyi; Zhang, Dengsong, E-mail: dszhang@shu.edu.cn

    2016-11-30

    Highlights: • MnO{sub x}-FeO{sub y}/Ce{sub 0.75}Zr{sub 0.25}O{sub 2} catalyst has a strong NO oxidation ability. • A high dispersion of active components is achieved on catalyst surface. • At high temperatures, bidentate nitrate is the common active species. • The addition of Fe can improve the reactivity of gaseous NO{sub 2} and bridged nitrates. - Abstract: A series of MnO{sub x}-MO{sub y}/Ce{sub 0.75}Zr{sub 0.25}O{sub 2} (M = Fe, Co, Ni, Cu) catalysts were synthesized by an impregnation method and used for selective catalytic reduction (SCR) of NO{sub x} with NH{sub 3}. The catalytic performances of various MnO{sub x}-MO{sub y}/Ce{sub 0.75}Zr{sub 0.25}O{sub 2} catalysts were studied. It was found that MnO{sub x}-FeO{sub y}/Ce{sub 0.75}Zr{sub 0.25}O{sub 2} catalyst showed excellent low-temperature activity and a broad temperature window. The catalysts were characterized by N{sub 2} adsorption/desorption, X-ray diffraction, X-ray photoelectron spectroscopy and in situ diffuse reflectance infrared transform spectroscopy (DRIFTS). Characterization of the catalyst confirmed the addition of iron oxide can enhance the NO oxidation ability of the catalyst which results in the outstanding low-temperature SCR activity. Meanwhile, iron oxides were well dispersed on catalyst surface which could avoid the agglomeration of active species, contributing to the strong interaction between active species and the support. More importantly, in situ DRIFTS results confirmed that bidentate nitrates are general active species on these catalysts, whereas the reactivity of gaseous NO{sub 2} and bridged nitrates got improved because of the addition of Fe.

  7. The redox processes in Hg-contaminated soils from Descoberto (Minas Gerais, Brazil): implications for the mercury cycle.

    Science.gov (United States)

    Windmöller, Cláudia C; Durão Júnior, Walter A; de Oliveira, Aline; do Valle, Cláudia M

    2015-02-01

    Investigations of the redox process and chemical speciation of Hg(II) lead to a better understanding of biogeochemical processes controlling the transformation of Hg(II) into toxic and bioaccumulative monomethyl mercury, mainly in areas contaminated with Hg(0). This study investigates the speciation and redox processes of Hg in soil samples from a small area contaminated with Hg(0) as a result of gold mining activities in the rural municipality of Descoberto (Minas Gerais, Brazil). Soil samples were prepared by adding Hg(0) and HgCl2 separately to dry soil, and the Hg redox process was monitored using thermodesorption coupled to atomic absorption spectrometry. A portion of the Hg(0) added was volatilized (up to 37.4±2.0%) or oxidized (from 36±7% to 88±16%). A correlation with Mn suggests that this oxidation is favored, but many other factors must be evaluated, such as the presence of microorganisms and the types of organic matter present. The interaction of Hg with the matrix is suggested to involve Hg(II)-complexes formed with inorganic and organic sulfur ligands and/or nonspecific adsorption onto oxides of Fe, Al and/or Mn. The kinetics of the oxidation reaction was approximated for two first-order reactions; the faster reaction was attributed to the oxidation of Hg(0)/Hg(I), and the slower reaction corresponded to Hg(I)/Hg(II). The second stage was 43-139 times slower than the first. The samples spiked with Hg(II) showed low volatilization and a shifting of the signal of Hg(II) to lower temperatures. These results show that the extent, rate and type of redox process can be adverse in soils. Descoberto can serve as an example for areas contaminated with Hg(0).

  8. Electrochemical Studies of Passive Film Stability on Fe49.7Cr17.7Mn1.9Mo7.4W1.6B15.2C3.8Si2.4 Amorphous Metal in Seawater at 90oCElectrochemical Studies of Passive Film Stability on Fe49.7Cr17.7Mn1.9Mo7.4W1.6B15.2C3.8Si2.4 Amorphous Metal in Seawater at 9

    Energy Technology Data Exchange (ETDEWEB)

    Farmer, J C; Haslam, J; Day, S D; Lian, T; Saw, C K; Hailey, P D; Choi, J S; Rebak, R B; Yang, N; Payer, J H; Perepezko, J H; Hildal, K; Lavernia, E J; Ajdelsztajn, L; Branagan, D J; Buffa, E J; Aprigliano, L F

    2007-04-25

    An iron-based amorphous metal, Fe{sub 49.7}Cr{sub 17.7}Mn{sub 1.9}Mo{sub 7.4}W{sub 1.6}B{sub 15.2}C{sub 3.8}Si{sub 2.4} (SAM2X5), with very good corrosion resistance was developed. This material was prepared as a melt-spun ribbon, as well as gas atomized powder and a thermal-spray coating. During electrochemical testing in several environments, including seawater at 90 C, the passive film stability was found to be comparable to that of high-performance nickel-based alloys, and superior to that of stainless steels, based on electrochemical measurements of the passive film breakdown potential and general corrosion rates. This material also performed very well in standard salt fog tests. Chromium (Cr), molybdenum (Mo) and tungsten (W) provided corrosion resistance, and boron (B) enabled glass formation. The high boron content of this particular amorphous metal made it an effective neutron absorber, and suitable for criticality control applications. This material and its parent alloy maintained corrosion resistance up to the glass transition temperature, and remained in the amorphous state during exposure to relatively high neutron doses.

  9. Density functional study of magnetic exchange of dinuclear manganese complexes with the heteropoly-molyanion:[MnII2(Xn+Mo9O33)2]2(n-10)- (X=PV, AsV, SeVI)

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    The magnetic exchange interactions between the dimanganese(II)-substituted complexes and the het-eropolymolyanion, [MnII2(Xn+Mo9O33)2]2(n-10)-(X = PV(I), AsV(II) and SeVI(III)), are investigated by using density functional theory combined with broken-symmetry approach (DFT-BS) method. The calculated magnetic exchange coupling constant (J) of complex II is in reasonable agreement with the responding experimental value and the negative J values indicate that antiferromagnetic exchange interactions exist in these complexes. Furthermore, the influence of the central heteroatom on the exchange cou-pling within the dimanganese core unit is studied from standpoints of geometry, spin density and fron-tier orbitals. It demonstrates that the change of the heteroatom X via PV-AsV-SeVI elongates the dis-tances of Mn1···Mn2 and shortens the distances of Ob···Ob, and reduces the effectiveness of the super-exchange pathways, consequently, decreasing the magnitude of the antiferromagnetic coupling constant, J, of these species.

  10. Adsorption and oxidation of elemental mercury over Ce-MnOx/Ti-PILCs.

    Science.gov (United States)

    He, Chuan; Shen, Boxiong; Chen, Jianhong; Cai, Ji

    2014-07-15

    A series of innovative Ce-Mn/Ti-pillared-clay (Ce-Mn/Ti-PILC) catalysts combining the advantages of PILCs and Ce-Mn were investigated for elemental mercury (Hg0) capture at 100-350 °C in the absence of HCl in the flue gas. The fresh and used catalysts were characterized by scanning electron microscopy (SEM), nitrogen adsorption-desorption, X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). The catalyst characterization indicated that the 6%Ce-6%MnOx/Ti-PILC catalyst possessed a large specific surface area and high dispersion of Ce and Mn on the surface. The experimental results indicated that the 6%Ce-6%MnOx/Ti-PILC catalyst exhibited high Hg0 capture (>90%) at 100-350 °C. During the first stage of the reaction, the main Hg0 capture mechanism for the catalyst was adsorption. As the reaction proceeded, the Hg0 oxidation ability was substantially enhanced. Both the hydroxyl oxygen and the lattice oxygen on the surface of the catalysts participated in Hg0 oxidation. At a low temperature (150 °C), the hydroxyl oxygen and lattice oxygen from Ce4+→Ce3+ and Mn3+→Mn2+ on the surface contributed to Hg0 oxidation. However, at a high temperature (250 °C), the hydroxyl oxygen and lattice oxygen from Mn4+→Mn3+ contributed to Hg0 oxidation. Hg0 oxidation was preferred at a high temperature. The 6%Ce-6%MnOx/Ti-PILC catalyst was demonstrated to a good Hg0 adsorbent and catalytic oxidant in the absence of HCl in the flue gas.

  11. Hg and As Minerals in Fluid Inclusions from the Williams Mine, Hemlo, and Their Genetic Implications

    Institute of Scientific and Technical Information of China (English)

    LU HUANZHANG(卢焕章); JAYANTA. GUHA; DON. C. HARRIS

    2002-01-01

    The Hemlo mineralization is enigmatic compared to general Archean lode gold deposits based on the fact that it is characterized by an exotic mineralogy containing elements such as As, Hg, Sb, Ba, V and Mo. The genetic concepts range from syngenetic to epigenetic types of mineralization. This reconnaissance study was designed to examine the relationship of Hg-As minerals with respect to fluid inclusions in the Williams mine (formerly known as the Page Williams mine) covering the A and C ore zones.

  12. Effects of properties of manganese oxide-impregnated catalysts and flue gas condition on multipollutant control of Hg{sup 0} and NO

    Energy Technology Data Exchange (ETDEWEB)

    Chiu, Chun-Hsiang [Institute of Environmental Engineering and Management, National Taipei University of Technology, No. 1, Sec. 3, Chung-Hsiao E. Rd., Taipei 106, Taiwan (China); Hsi, Hsing-Cheng, E-mail: hchsi@ntu.edu.tw [Graduate Institute of Environmental Engineering, National Taiwan University, No. 71, Chou-Shan Rd., Taipei 106, Taiwan (China); Lin, Hong-Ping [Department of Chemistry, National Cheng-Kung University, No. 1, University Rd., Tainan 701, Taiwan (China); Chang, Tien-Chin [Institute of Environmental Engineering and Management, National Taipei University of Technology, No. 1, Sec. 3, Chung-Hsiao E. Rd., Taipei 106, Taiwan (China)

    2015-06-30

    Highlights: • MnO{sub x} impregnation caused changes in physical/chemical properties of catalyst. • Mn{sup 4+} was the main valence state of impregnated MnO{sub x}. • MnO{sub x} impregnation enhanced the removal of Hg{sup 0}/NO/SO{sub 2} with SCR catalyst. • HCl, O{sub 2}, and SO{sub 2} at ≤200 ppm and elevating temperature promoted Hg{sup 0} oxidation. • Increasing NO and NH{sub 3} concentrations reduced Hg{sup 0} oxidation. - Abstract: This research investigated the effects of manganese oxide (MnO{sub x}) impregnation on the physical/chemical properties and multi pollutant control effectiveness of Hg{sup 0} and NO using a V{sub 2}O{sub 5}–WO{sub 3}/TiO{sub 2}–SiO{sub 2} selective catalytic reduction (SCR) catalyst. Raw and MnO{sub x}-treated SCR samples were bean-shaped nanoparticles with sizes within 10–30 nm. Impregnating MnO{sub x} of ≤5 wt% caused limited changes in physical properties of the catalyst. The decrease in surface area when the impregnated MnO{sub x} amount was 10 wt% may stem from the pore blockage and particle growth or aggregation of the catalyst. Mn{sup 4+} was the main valence state of impregnated MnO{sub x}. Apparent crystallinity of MnO{sub x} was not observed based on X-ray diffraction. MnO{sub x} impregnation enhanced the Hg{sup 0} oxidation and NO/SO{sub 2} removal of SCR catalyst. The 5 and 10% MnO{sub x}-impregnated samples had the greatest multi pollutant control potentials for Hg{sup 0} oxidation and NO removal; however, the increasing SO{sub 2} removal that may be mainly due to SO{sub 2}–SO{sub 3} conversion should be cautioned. HCl and O{sub 2} greatly promoted Hg{sup 0} oxidation. SO{sub 2} enhanced Hg{sup 0} oxidation at ≤200 ppm while NO and NH{sub 3} consistently inhibited Hg{sup 0} oxidation. Elevating flue gas temperature enhanced Hg{sup 0} oxidation. Overall, MnO{sub x}-impregnated catalysts show stable and consistent multi pollutant removal effectiveness under the test conditions.

  13. Mechanistic studies of mercury adsorption and oxidation by oxygen over spinel-type MnFe2O4.

    Science.gov (United States)

    Yang, Yingju; Liu, Jing; Zhang, Bingkai; Liu, Feng

    2017-01-05

    MnFe2O4 has been regarded as a very promising sorbent for mercury emission control in coal-fired power plants because of its high adsorption capacity, magnetic, recyclable and regenerable properties. First-principle calculations based on density functional theory (DFT) were used to elucidate the mercury adsorption and oxidation mechanisms on MnFe2O4 surface. DFT calculations show that Mn-terminated MnFe2O4 (1 0 0) surface is much more stable than Fe-terminated surface. Hg(0) is physically adsorbed on Fe-terminated MnFe2O4 (1 0 0) surface. Hg(0) adsorption on Mn-terminated MnFe2O4 (1 0 0) surface is a chemisorption process. The partial density of states (PDOS) analysis indicates that Hg atom interacts strongly with surface Mn atoms through the orbital hybridization. HgO is adsorbed on the MnFe2O4 surface in a chemical adsorption manner. The small HOMO-LUMO energy gap implies that HgO molecular shows high chemical reactivity for HgO adsorption on MnFe2O4 surface. The energy barriers of Hg(0) oxidation by oxygen on Fe- and Mn-terminated MnFe2O4 surfaces are 206.37 and 76.07kJ/mol, respectively. Mn-terminated surface is much more favorable for Hg(0) oxidation than Fe-terminated surface. In the whole Hg(0) oxidation process, the reaction between adsorbed mercury and surface oxygen is the rate-determining step.

  14. Effect of Bi2O3-MoO3-Nb2O5 Addition on Microstructure and Magnetic Properties of Mn-Zn Ferrites with High Permeability%复合添加剂Bi2O3-MoO3-Nb2O5对高磁导率Mn-Zn铁氧体微观结构与磁性能的影响

    Institute of Scientific and Technical Information of China (English)

    孙玉坤; 李冬云; 高朋召; 徐扬; 葛洪良; 颜冲

    2016-01-01

    采用高温固相反应制备了 Bi2O3–MoO3–Nb2O5复合掺杂高磁导率 Mn–Zn 铁氧体材料,利用扫描电子显微镜、B–H测量仪和阻抗分析仪等对材料结构和性能进行表征,研究了不同含量MoO3复合添加剂Bi2O3–MoO3–Nb2O5对Mn–Zn铁氧体微观结构和磁性能的影响。结果表明:复合添加剂Bi2O3–MoO3–Nb2O5中,适量的MoO3可以有效改善材料的微观结构,提升材料起始磁导率,降低材料比损耗,提升材料饱和磁感应强度,并在Nb2O5=0.020%(质量分数)、Bi2O3=0.015%、MoO3=0.030%时,材料获得最佳的综合性能:起始磁导率μi=12457.51,tanδ/μi=3.76×10–6,饱和磁感应强度Bs=0.416 T。%Mn–Zn ferrites as important magnetic ceramics are widely used due to their low power loss and high initial permeability. Small amounts of oxide additives can greatly affect the properties of ferrites. The additives have a different effect on the microstructure and magnetic properties of Mn–Zn ferrites. In this paper, the Bi2O3–MoO3–Nb2O5 doped a high permeability Mn–Zn ferrites with different MoO3 contents were prepared via high temperature solid state reactions, and the effect of MoO3 on the microstructure and magnetic properties of Mn–Zn ferrites was investigated by scanning electron microscope, B–H tester and impendence analyzer, respectively. The results show that a suitable amount of MoO3 in Bi2O3–MoO3–Nb2O5 co-dopant can improve the microstructure, reduce the specific losses and enhance the saturation induction density of Mn–Zn ferrites effectively. The optimum performance (i.e., initial permeabilityμi=12 457.51;specific loss coefficient tanδ/μi=3.76×10–6;saturation induction density Bs=0.416 T) was obtained at the contents of Nb2O5, Bi2O3 and MoO3 of 0.020%(in mass fraction), 0.015%and 0.030%.

  15. Effect of Mo on stability of quasicrystalline phase in Al–Mn–Fe alloy

    Energy Technology Data Exchange (ETDEWEB)

    Stan, Katarzyna, E-mail: k.stan@imim.pl [Institute of Metallurgy and Materials Science, Polish Academy of Sciences, Krakow 30-059, 25, Reymonta St. (Poland); Lityńska-Dobrzyńska, Lidia [Institute of Metallurgy and Materials Science, Polish Academy of Sciences, Krakow 30-059, 25, Reymonta St. (Poland); Lábár, János L. [Institute for Technical Physics and Materials Science, Research Centre for Natural Sciences, Hungarian Academy of Sciences, H-1121 Budapest, Konkoly-Thege ut 29-33 (Hungary); Góral, Anna [Institute of Metallurgy and Materials Science, Polish Academy of Sciences, Krakow 30-059, 25, Reymonta St. (Poland)

    2014-02-15

    Highlights: ► Microstructure evolution of melt spun Al–Mn–Fe–Mo ribbon after annealing was studied. ► In as spun state quasicrystals enriched in Fe, Mn and Mo coexist with α-(Al). ► After annealing Al{sub 6}(Mn, Fe) and Al{sub 12}(Mn, Mo) phases were formed. ► Small addition of Mo improves thermal stability of quasicrystals in Al–Mn–Fe alloy. -- Abstract: Microstructure evolution in rapidly solidified Al{sub 91}Mn{sub 6}Fe{sub 2}Mo{sub 1} ribbons after annealing was investigated using X-ray diffraction, scanning electron microscopy and analytical transmission electron microscopy including in situ heating experiment in TEM. As spun ribbons consisted of icosahedral quasicrystalline particles enriched in Fe, Mn and Mo embedded in an aluminium matrix. A small amount of quasicrystals containing Fe and Mn which coexisted with the Al{sub 3}(Fe, Mn) phase was also observed between the aluminium grains. Further annealing experiments and subsequent analysis of microstructure changes in the sample showed that the quasicrystalline particles underwent a transformation into stable crystalline phases at temperatures which depended on their composition. It was observed that quasicrystals enriched in Mn and Fe transformed at much lower temperatures than primary quasicrystals with Mo content. It was noticed that two different crystalline phases formed in dependence on the temperature of annealing. The Al{sub 6}(Mn, Fe) phase appeared first at the quasicrystal/matrix interface. At higher temperature, the Al{sub 12}(Mn, Mo) phase formed due to reaction of the Al{sub 6}(Mn, Fe) phase with the aluminium matrix. Microstructural and DSC investigations showed that addition of molybdenum improved thermal stability of the quasicrystals in Al–Mn–Fe system.

  16. Quantification of corrosion resistance of a new-class of criticality control materials: thermal-spray coatings of high-boron iron-based amorphous metals - Fe49.7Cr17.7Mn1.9Mo7.4W1.6B15.2C3.8Si2.4

    Energy Technology Data Exchange (ETDEWEB)

    Farmer, J C; Choi, J S; Shaw, C K; Rebak, R; Day, S D; Lian, T; Hailey, P; Payer, J H; Branagan, D J; Aprigliano, L F

    2007-03-28

    An iron-based amorphous metal, Fe{sub 49.7}Cr{sub 17.7}Mn{sub 1.9}Mo{sub 7.4}W{sub 1.6}B{sub 15.2}C{sub 3.8}Si{sub 2.4} (SAM2X5), with very good corrosion resistance was developed. This material was produced as a melt-spun ribbon, as well as gas atomized powder and a thermal-spray coating. Chromium (Cr), molybdenum (Mo) and tungsten (W) provided corrosion resistance, and boron (B) enabled glass formation. The high boron content of this particular amorphous metal made it an effective neutron absorber, and suitable for criticality control applications. Earlier studies have shown that ingots and melt-spun ribbons of these materials have good passive film stability in these environments. Thermal spray coatings of these materials have now been produced, and have undergone a variety of corrosion testing, including both atmospheric and long-term immersion testing. The modes and rates of corrosion have been determined in the various environments, and are reported here.

  17. Measurement of the Single Top Quark Production Cross Section and <mo stretchy='false'>|mo>Vtb<mo stretchy='false'>|mo> in Events with One Charged Lepton, Large Missing Transverse Energy, and Jets at CDF

    Energy Technology Data Exchange (ETDEWEB)

    Aaltonen, T.; 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.; 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.; Butti, P.; Buzatu, A.; Calamba, A.; Camarda, S.; Campanelli, M.; Canelli, F.; Carls, B.; Carlsmith, D.; Carosi, R.; Carrillo, S.; Casal, B.; Casarsa, M.; Castro, A.; Catastini, P.; Cauz, D.; Cavaliere, V.; Cerri, A.; Cerrito, L.; Chen, Y. C.; Chertok, M.; Chiarelli, G.; Chlachidze, G.; Cho, K.; Chokheli, D.; Clark, A.; Clarke, C.; Convery, M. E.; Conway, J.; Corbo, M.; Cordelli, M.; Cox, C. A.; Cox, D. J.; Cremonesi, M.; Cruz, D.; Cuevas, J.; Culbertson, R.; d’Ascenzo, N.; Datta, M.; de Barbaro, P.; Demortier, L.; Deninno, M.; D’Errico, M.; Devoto, F.; Di Canto, A.; Di Ruzza, B.; Dittmann, J. R.; Donati, S.; D’Onofrio, M.; Dorigo, M.; Driutti, A.; Ebina, K.; Edgar, R.; Elagin, A.; Erbacher, R.; Errede, S.; Esham, B.; Farrington, S.; Fernández Ramos, J. P.; Field, R.; Flanagan, G.; Forrest, R.; Franklin, M.; Freeman, J. C.; Frisch, H.; Funakoshi, Y.; Galloni, C.; Garfinkel, A. F.; Garosi, P.; Gerberich, H.; Gerchtein, E.; Giagu, S.; Giakoumopoulou, V.; Gibson, K.; Ginsburg, C. M.; Giokaris, N.; Giromini, P.; Glagolev, V.; Glenzinski, D.; Gold, M.; Goldin, D.; Golossanov, A.; Gomez, G.; Gomez-Ceballos, G.; Goncharov, M.; González López, O.; Gorelov, I.; Goshaw, A. T.; Goulianos, K.; Gramellini, E.; Grosso-Pilcher, C.; Group, R. C.; Guimaraes da Costa, J.; Hahn, S. R.; Han, J. Y.; Happacher, F.; Hara, K.; Hare, M.; Harr, R. F.; Harrington-Taber, T.; Hatakeyama, K.; Hays, C.; Heinrich, J.; Herndon, M.; Hirschbuehl, D.; Hocker, A.; Hong, Z.; Hopkins, W.; Hou, S.; Hughes, R. E.; Husemann, U.; 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.; Kambeitz, M.; Kamon, T.; Karchin, P. E.; Kasmi, A.; Kato, Y.; Ketchum, W.; Keung, J.; 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.; Knoepfel, K.; Kondo, K.; Kong, D. J.; Konigsberg, J.; Kotwal, A. V.; Kreps, M.; Kroll, J.; Kruse, M.; Kuhr, T.; Kurata, M.; Laasanen, A. T.; Lammel, S.; Lancaster, M.; Lannon, K.; Latino, G.; Lee, H. S.; Lee, J. S.; Leo, S.; Leone, S.; Lewis, J. D.; Limosani, A.; Lipeles, E.; Lister, A.; Liu, H.; Liu, Q.; Liu, T.; Lockwitz, S.; Loginov, A.; Lucchesi, D.; Lucà, A.; Lueck, J.; Lujan, P.; Lukens, P.; Lungu, G.; Lys, J.; Lysak, R.; Madrak, R.; Maestro, P.; Malik, S.; Manca, G.; Manousakis-Katsikakis, A.; Marchese, L.; Margaroli, F.; Marino, P.; Matera, K.; Mattson, M. E.; Mazzacane, A.; Mazzanti, P.; McNulty, R.; Mehta, A.; Mehtala, P.; Mesropian, C.; Miao, T.; Mietlicki, D.; Mitra, A.; Miyake, H.; Moed, S.; Moggi, N.; Moon, C. S.; Moore, R.; Morello, M. J.; Mukherjee, A.; Muller, Th.; Murat, P.; Mussini, M.; Nachtman, J.; Nagai, Y.; Naganoma, J.; Nakano, I.; Napier, A.; Nett, J.; Neu, C.; Nigmanov, T.; Nodulman, L.; Noh, S. Y.; Norniella, O.; Oakes, L.; Oh, S. H.; Oh, Y. D.; Oksuzian, I.; Okusawa, T.; Orava, R.; Ortolan, L.; Pagliarone, C.; Palencia, E.; Palni, P.; Papadimitriou, V.; Parker, W.; Pauletta, G.; Paulini, M.; Paus, C.; Phillips, T. J.; Pianori, E.; Pilot, J.; Pitts, K.; Plager, C.; Pondrom, L.; Poprocki, S.; Potamianos, K.; Pranko, A.; Prokoshin, F.; Ptohos, F.; Punzi, G.; Redondo Fernández, I.; Renton, P.; Rescigno, M.; Rimondi, F.; Ristori, L.; Robson, A.; Rodriguez, T.; Rolli, S.; Ronzani, M.; Roser, R.; Rosner, J. L.; Ruffini, F.; Ruiz, A.; Russ, J.; Rusu, V.; Sakumoto, W. K.; Sakurai, Y.; Santi, L.; Sato, K.; Saveliev, V.; Savoy-Navarro, A.; Schlabach, P.; Schmidt, E. E.; Schwarz, T.; Scodellaro, L.; 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.; Sliwa, K.; Smith, J. R.; Snider, F. D.; Song, H.; Sorin, V.; St. Denis, R.; Stancari, M.; Stentz, D.; Strologas, J.; Sudo, Y.; Sukhanov, A.; Suslov, I.; Takemasa, K.; Takeuchi, Y.; Tang, J.; Tecchio, M.; Teng, P. K.; Thom, J.; Thomson, E.; Thukral, V.; Toback, D.; Tokar, S.; Tollefson, K.; Tomura, T.; Tonelli, D.; Torre, S.; Torretta, D.; Totaro, P.; Trovato, M.; Ukegawa, F.; Uozumi, S.; Vázquez, F.; Velev, G.; Vellidis, C.; Vernieri, C.; Vidal, M.; Vilar, R.; Vizán, J.; Vogel, M.; Volpi, G.; Wagner, P.; Wallny, R.; Wang, S. M.; Waters, D.; Wester, W. C.; Whiteson, D.; Wicklund, A. B.; Wilbur, S.; 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.; Zanetti, A. M.; Zeng, Y.; Zhou, C.; Zucchelli, S.

    2014-12-31

    We report a measurement of single top quark production in proton-antiproton collisions at a center-of-mass energy of smo>=>1.96mn> TeV using a data set corresponding to mn>7.5mn> fbmo>->1mn> of integrated luminosity collected by the Collider Detector at Fermilab. We select events consistent with the single top quark decay process tmo stretchy="false">→mo>Wbmo stretchy="false">→mo>mo>ℓmo>νb by requiring the presence of an electron or muon, a large imbalance of transverse momentum indicating the presence of a neutrino, and two or three jets including at least one originating from a bottom quark. An artificial neural network is used to discriminate the signal from backgrounds. We measure a single top quark production cross section of mn>3.0mn>>4mn>mo>->0.53mn>mo>+>0.57mn> pb and set a lower limit on the magnitude of the coupling between the top quark and bottom quark mo stretchy="false">|mo>

  18. Chemical stabilization and high pressure synthesis of Ba-free Hg-based superconductors, (Hg,M)Sr{sub 2}Ca{sub n-1}Cu{sub n}O{sub y}(N=1{approximately}3)

    Energy Technology Data Exchange (ETDEWEB)

    Kishio, K. [Univ. of Tokyo (Japan)]|[Kyoto Univ. (Japan); Shimoyama, J.; Hahakura, S. [Univ. of Tokyo (Japan)] [and others

    1994-12-31

    A homologous series of new Hg-based HTSC compounds, (Hg,M)Sr{sub 2}Ca{sub n-1}Cu{sub n}O{sub y} with n=1 to 3, have been synthesized. The stabilization of the pure phases have been accomplished by chemical doping of third elements such as M=Cr, Mo and Re. While the Hg1201(n=1) phase was readily obtained in this way, it was necessary to simultaneously dope Y into the Ca site to stabilize the Hg1212(n=2) phase. On the other hand, single-phase Y-free Hg1212(n=2) and Hg1223(n=3) samples were synthesized only under a high pressure of 6 GPa. In sharp contrast to the Ba-containing compounds, all the samples prepared in the present study have been quite stable during the synthesis and no deterioration in air has been observed after the preparation.

  19. Chemical thermodynamics of the Hg1212 phase

    Science.gov (United States)

    Tsuchiya, Tetsuo; Fueki, Kazuo

    1997-02-01

    The single phase of Hg1212 was synthesized by the simple oxide method using starting materials containing HgO 16% in excess. Stability regions of Hg1212 and pure HgO were determined by measuring the decomposition temperature as a function of oxygen partial pressure, and thermodynamic diagrams showing the stability domains of HgO and Hg1212 were constructed. The thermodynamical condition of formation of Hg1212 was discussed using the diagrams. It was found by chemical analysis that the valence of Hg is always 2 + and the valence of Ce changes with the oxygen content. TC (zero) changed from 122 to 118 K when the oxygen content was increased from 6.10 to 6.22.

  20. Pu<mn>236mn><mo>(mo>n<mo>,f)> , Pu<mn>237mn><mo>(mo>n<mo>,f)> , and Pu<mn>238mn><mo>(mo>n<mo>,f)> cross sections deduced from <mo>(mo>p<mo>,t)> , <mo>(mo>p<mo>,d)> , and <mo>(mo>p<mo>,mo>p<mo>')> surrogate reactions

    Energy Technology Data Exchange (ETDEWEB)

    Hughes, R. O. [Univ. of Richmond, VA (United States); Beausang, C. W. [Univ. of Richmond, VA (United States); Ross, T. J. [Univ. of Richmond, VA (United States); Burke, J. T. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Casperson, R. J. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Cooper, N. [Yale Univ., New Haven, CT (United States); Escher, J. E. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Gell, K. [Univ. of Richmond, VA (United States); Good, E. [Univ. of Richmond, VA (United States); Humby, P. [Yale Univ., New Haven, CT (United States); McCleskey, M. [Texas A & M Univ., College Station, TX (United States); Saastimoinen, A. [Texas A & M Univ., College Station, TX (United States); Tarlow, T. D. [Univ. of Richmond, VA (United States); Thompson, I. J. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

    2014-07-01

    The Pu236(n,f), Pu237(n,f) and Pu238(n,f) cross sections have been inferred by utilizing the surrogate ratio method. Targets of Pu239 and U235 were bombarded with 28.5-MeV protons, and the light ion recoils, as well as fission fragments, were detected using the STARS detector array at the K150 Cyclotron at the Texas A&M cyclotron facility. The (p, tf) reaction on Pu239 and U235 targets was used to deduce the σ (Pu236(n,f))/σ(U232(n,f)) ratio, and the Pu236(n,f) cross section was subsequently determined for En=0.5–7.5 MeV. Similarly, the (p,df) reaction on the same two targets was used to deduce the σ(Pu237(n,f))/σ(U233(n,f)) ratio, and the Pu237(n,f) cross section was extracted in the energy range En=0.5–7 MeV. The Pu238(n,f) cross section was also deduced by utilizing the (p,p') reaction channel on the same targets. There is good agreement with the recent ENDF/B-VII.1 evaluated cross section data for Pu238(n,f) in the range En=0.5–10.5 MeV and for Pu237(n,f) in the range En=0.5–7 MeV; however, the Pu236(n,f) cross section deduced in the present work is higher than the evaluation between 2 and 7 MeV.

  1. A laboratory-incubated redox oscillation experiment to investigate Hg fluxes from highly contaminated coastal marine sediments (Gulf of Trieste, Northern Adriatic Sea).

    Science.gov (United States)

    Emili, A; Carrasco, L; Acquavita, A; Covelli, S

    2014-03-01

    Mercury (Hg) mobility at the sediment-water interface was investigated during a laboratory incubation experiment conducted with highly contaminated sediments (13 μg g(-1)) of the Gulf of Trieste. Undisturbed sediment was collected in front of the Isonzo River mouth, which inflows Hg-rich suspended material originating from the Idrija (NW Slovenia) mining district. Since hypoxic and anoxic conditions at the bottom are frequently observed and can influence the Hg biogeochemical behavior, a redox oscillation was simulated in the laboratory, at in situ temperature, using a dark flux chamber. Temporal variations of several parameters were monitored simultaneously: dissolved Hg (DHg) and methylmercury (MeHg), O2, NH4 (+), NO3 (-) + NO2 (-), PO4 (3-), H2S, dissolved Mn(2+), dissolved inorganic and organic carbon (DIC and DOC). Under anoxic conditions, both Hg (665 ng m(2) day(-1)) and MeHg (550 ng m(2) day(-1)) fluxed from sediments into the water column, whereas re-oxygenation caused concentrations of MeHg and Hg to rapidly drop, probably due to re-adsorption onto Fe/Mn-oxyhydroxides and enhanced demethylation processes. Hence, during anoxic events, sediments of the Gulf of Trieste may be considered as an important source of DHg species for the water column. On the contrary, re-oxygenation of the bottom compartment mitigates Hg and MeHg release from the sediment, thus acting as a natural "defence" from possible interaction between the metal and the aquatic organisms.

  2. Measurement of the forward-backward asymmetry in top quark-antiquark production in pp<mo accent='true' stretchy='false'>¯mo> collisions using the lepton<mo mathvariant='bold'>+mo>jets channel

    Energy Technology Data Exchange (ETDEWEB)

    Abazov, V. M.; Abbott, B.; Acharya, B. S.; Adams, M.; Adams, T.; Agnew, J. P.; Alexeev, G. D.; Alkhazov, G.; Alton, A.; Askew, A.; Atkins, S.; Augsten, K.; Avila, C.; Badaud, F.; Bagby, L.; Baldin, B.; Bandurin, D. V.; Banerjee, S.; Barberis, E.; Baringer, P.; Bartlett, J. F.; Bassler, U.; Bazterra, V.; Bean, A.; Begalli, M.; Bellantoni, L.; Beri, S. B.; Bernardi, G.; Bernhard, R.; Bertram, I.; Besançon, M.; Beuselinck, R.; Bhat, P. C.; Bhatia, S.; Bhatnagar, V.; Blazey, G.; Blessing, S.; Bloom, K.; Boehnlein, A.; Boline, D.; Boos, E. E.; Borissov, G.; Borysova, M.; Brandt, A.; Brandt, O.; Brock, R.; Bross, A.; Brown, D.; Bu, X. B.; Buehler, M.; Buescher, V.; Bunichev, V.; Burdin, S.; Buszello, C. P.; Camacho-Pérez, E.; Casey, B. C. K.; Castilla-Valdez, H.; Caughron, S.; Chakrabarti, S.; Chan, K. M.; Chandra, A.; Chapon, E.; Chen, G.; Cho, S. W.; Choi, S.; Choudhary, B.; Cihangir, S.; Claes, D.; Clutter, J.; Cooke, M.; Cooper, W. E.; Corcoran, M.; Couderc, F.; Cousinou, M. -C.; Cutts, D.; Das, A.; Davies, G.; de Jong, S. J.; De La Cruz-Burelo, E.; Déliot, F.; Demina, R.; Denisov, D.; Denisov, S. P.; Desai, S.; Deterre, C.; DeVaughan, K.; Diehl, H. T.; Diesburg, M.; Ding, P. F.; Dominguez, A.; Dubey, A.; Dudko, L. V.; Duperrin, A.; Dutt, S.; Eads, M.; Edmunds, D.; Ellison, J.; Elvira, V. D.; Enari, Y.; Evans, H.; Evdokimov, V. N.; Falkowski, A.; Fauré, A.; Feng, L.; Ferbel, T.; Fiedler, F.; Filthaut, F.; Fisher, W.; Fisk, H. E.; Fortner, M.; Fox, H.; Fuess, S.; Garbincius, P. H.; Garcia-Bellido, A.; García-González, J. A.; Gavrilov, V.; Geng, W.; Gerber, C. E.; Gershtein, Y.; Ginther, G.; Gogota, O.; Golovanov, G.; Grannis, P. D.; Greder, S.; Greenlee, H.; Grenier, G.; Gris, Ph.; Grivaz, J. -F.; Grohsjean, A.; Grünendahl, S.; Grünewald, M. W.; Guillemin, T.; Gutierrez, G.; Gutierrez, P.; Haley, J.; Han, L.; Harder, K.; Harel, A.; Hauptman, J. M.; Hays, J.; Head, T.; Hebbeker, T.; Hedin, D.; Hegab, H.; Heinson, A. P.; Heintz, U.; Hensel, C.; Heredia-De La Cruz, I.; Herner, K.; Hesketh, G.; Hildreth, M. D.; Hirosky, R.; Hoang, T.; Hobbs, J. D.; Hoeneisen, B.; Hogan, J.; Hohlfeld, M.; Holzbauer, J. L.; Howley, I.; Hubacek, Z.; Hynek, V.; Iashvili, I.; Ilchenko, Y.; Illingworth, R.; Ito, A. S.; Jabeen, S.; Jaffré, M.; Jayasinghe, A.; Jeong, M. S.; Jesik, R.; Jiang, P.; Johns, K.; Johnson, E.; Johnson, M.; Jonckheere, A.; Jonsson, P.; Joshi, J.; Jung, A. W.; Juste, A.; Kajfasz, E.; Karmanov, D.; Katsanos, I.; Kehoe, R.; Kermiche, S.; Khalatyan, N.; Khanov, A.; Kharchilava, A.; Kharzheev, Y. N.; Kiselevich, I.; Kohli, J. M.; Kozelov, A. V.; Kraus, J.; Kumar, A.; Kupco, A.; Kurča, T.; Kuzmin, V. A.; Lammers, S.; Lebrun, P.; Lee, H. S.; Lee, S. W.; Lee, W. M.; Lei, X.; Lellouch, J.; Li, D.; Li, H.; Li, L.; Li, Q. Z.; Lim, J. K.; Lincoln, D.; Linnemann, J.; Lipaev, V. V.; Lipton, R.; Liu, H.; Liu, Y.; Lobodenko, A.; Lokajicek, M.; Lopes de Sa, R.; Luna-Garcia, R.; Lyon, A. L.; Maciel, A. K. A.; Madar, R.; Magaña-Villalba, R.; Malik, S.; Malyshev, V. L.; Mansour, J.; Martínez-Ortega, J.; McCarthy, R.; McGivern, C. L.; Meijer, M. M.; Melnitchouk, A.; Menezes, D.; Mercadante, P. G.; Merkin, M.; Meyer, A.; Meyer, J.; Miconi, F.; Mondal, N. K.; Mulhearn, M.; Nagy, E.; Narain, M.; Nayyar, R.; Neal, H. A.; Negret, J. P.; Neustroev, P.; Nguyen, H. T.; Nunnemann, T.; Orbaker, D.; Orduna, J.; Osman, N.; Osta, J.; Pal, A.; Parashar, N.; Parihar, V.; Park, S. K.; Partridge, R.; Parua, N.; Patwa, A.; Penning, B.; Perfilov, M.; Peters, Y.; Petridis, K.; Petrillo, G.; Pétroff, P.; Pleier, M. -A.; Podstavkov, V. M.; Popov, A. V.; Prewitt, M.; Price, D.; Prokopenko, N.; Qian, J.; Quadt, A.; Quinn, B.; Ratoff, P. N.; Razumov, I.; Ripp-Baudot, I.; Rizatdinova, F.; Rominsky, M.; Ross, A.; Royon, C.; Rubinov, P.; Ruchti, R.; Sajot, G.; Sánchez-Hernández, A.; Sanders, M. P.; Santos, A. S.; Savage, G.; Savitskyi, M.; Sawyer, L.; Scanlon, T.; Schamberger, R. D.; Scheglov, Y.; Schellman, H.; Schwanenberger, C.; Schwienhorst, R.; Sekaric, J.; Severini, H.; Shabalina, E.; Shary, V.; Shaw, S.; Shchukin, A. A.; Simak, V.; Skubic, P.; Slattery, P.; Smirnov, D.; Snow, G. R.; Snow, J.; Snyder, S.; Söldner-Rembold, S.; Sonnenschein, L.; Soustruznik, K.; Stark, J.; Stoyanova, D. A.; Strauss, M.; Suter, L.; Svoisky, P.; Titov, M.; Tokmenin, V. V.; Tsai, Y. -T.; Tsybychev, D.; Tuchming, B.; Tully, C.; Uvarov, L.; Uvarov, S.; Uzunyan, S.; Van Kooten, R.; van Leeuwen, W. M.; Varelas, N.; Varnes, E. W.; Vasilyev, I. A.; Verkheev, A. Y.; Vertogradov, L. S.; Verzocchi, M.; Vesterinen, M.; Vilanova, D.; Vokac, P.; Wahl, H. D.; Wang, M. H. L. S.; Warchol, J.; Watts, G.; Wayne, M.; Weichert, J.; Welty-Rieger, L.; Williams, M. R. J.; Wilson, G. W.; Wobisch, M.; Wood, D. R.; Wyatt, T. R.; Xie, Y.; Yamada, R.; Yang, S.; Yasuda, T.; Yatsunenko, Y. A.; Ye, W.; Ye, Z.; Yin, H.; Yip, K.; Youn, S. W.; Yu, J. M.; Zennamo, J.; Zhao, T. G.; Zhou, B.; Zhu, J.; Zielinski, M.; Zieminska, D.; Zivkovic, L.

    2014-10-01

    We present a measurement of the forward–backward asymmetry in top quark–antiquark production using the full Tevatron Run II data set collected by the D0 experiment at Fermilab. The measurement is performed in leptonmo>+mo>jets final states using a new kinematic fitting algorithm for events with four or more jets and a new partial reconstruction algorithm for events with only three jets. Corrected for detector acceptance and resolution effects, the asymmetry is evaluated to be AFBmo>= stretchy="false">(mo>>10.6mn>±>3.0mn> stretchy="false">)mo>mo>%>. Results are consistent with the standard model predictions which range from 5.0% to 8.8%. We also present the dependence of the asymmetry on the invariant mass of the top quark–antiquark system and the difference in rapidities of the top quark and antiquark.

  3. Effect of water vapor on the CO and CH_4 catalytic oxidation over CeO_2-MO_x (M=Cu, Mn, Fe, Co, and Ni) mixed oxide

    Institute of Scientific and Technical Information of China (English)

    乔东升; 卢冠忠; 郭耘; 王艳芹; 郭杨龙

    2010-01-01

    CeO2-MOx (M=Cu, Mn, Fe, Co, and Ni) mixed oxide catalysts were prepared by a citric acid complexation-combustion method. CeO2-MOx solid solutions could be formed with M cations doping into CeO2 lattice, while NiO and Co3O4 phases were detected on the surface of CeO2-NiO and CeO2-Co3O4 by Raman spectroscopy. The presence of M in CeO2 could obviously promote its catalytic activity for CH4 catalytic combustion and CO oxidation. Among the prepared samples, CeO2-CuO exhibited the best performance for CO oxidatio...

  4. Corrosion Resistance of Amorphous Fe49.7Cr17.7Mn1.9Mo7.4W1.6B15.2C3.8Si2.4 coating - a new criticality-controlled material

    Energy Technology Data Exchange (ETDEWEB)

    Farmer, J C; Choi, J S; Saw, C K; Rebak, R; Day, S D; Lian, T; Hailey, P; Payer, J H; Branagan, D J; Aprigliano, L F

    2007-03-28

    An iron-based amorphous metal with good corrosion resistance and a high absorption cross-section for thermal neutrons has been developed and is reported here. This amorphous alloy has the approximate formula Fe{sub 49.7}Cr{sub 17.7}Mn{sub 1.9}Mo{sub 7.4}W{sub 1.6}B{sub 15.2}C{sub 3.8}Si{sub 2.4} and is known as SAM2X5. Chromium (Cr), molybdenum (Mo) and tungsten (W) were added to provide corrosion resistance, while boron (B) was added to promote glass formation and the absorption of thermal neutrons. Since this amorphous metal has a higher boron content than conventional borated stainless steels, it provides the nuclear engineer with design advantages for criticality control structures with enhanced safety. While melt-spun ribbons with limited practical applications were initially produced, large quantities (several tons) of gas atomized powder have now been produced on an industrial scale, and applied as thermal-spray coatings on prototypical half-scale spent nuclear fuel containers and neutron-absorbing baskets. These prototypes and other SAM2X5 samples have undergone a variety of corrosion testing, including both salt-fog and long-term immersion testing. Modes and rates of corrosion have been determined in various relevant environments, and are reported here. While these coatings have less corrosion resistance than melt-spun ribbons and optimized coatings produced in the laboratory, substantial corrosion resistance has been achieved.

  5. Long-Term Corrosion Tests of Prototypical SAM2X5 (Fe49.7Cr17.7Mn1.9Mo7.4W1.6B15.2C3.8Si2.4) Coatings

    Energy Technology Data Exchange (ETDEWEB)

    Farmer, J C; Choi, J S; Saw, C K; Rebak, R H; Day, S D; Lian, T; Hailey, P D; Payer, J H; Branagan, D J; Aprigliano, L F

    2007-05-10

    An iron-based amorphous metal with good corrosion resistance and a high absorption cross-section for thermal neutrons has been developed and is reported here. This amorphous alloy has the approximate formula Fe{sub 49.7}Cr{sub 17.7}Mn{sub 1.9}Mo{sub 7.4}W{sub 1.6}B{sub 15.2}C{sub 3.8}Si{sub 2.4} and is known as SAM2X5. Chromium (Cr), molybdenum (Mo) and tungsten (W) were added to provide corrosion resistance, while boron (B) was added to promote glass formation and the absorption of thermal neutrons. Since this amorphous metal has a higher boron content than conventional borated stainless steels, it provides the nuclear engineer with design advantages for criticality control structures with enhanced safety. While melt-spun ribbons with limited practical applications were initially produced, large quantities (several tons) of gas atomized powder have now been produced on an industrial scale, and applied as thermal-spray coatings on prototypical half-scale spent nuclear fuel containers and neutron-absorbing baskets. These prototypes and other SAM2X5 samples have undergone a variety of corrosion testing, including both salt-fog and long-term immersion testing. The modes and rates of corrosion have been determined in the various environments, and are reported here. While these coatings have less corrosion resistance than melt-spun ribbons and optimized coatings produced in the laboratory, substantial corrosion resistance has been achieved.

  6. Folic acid functionalized silver nanoparticles with sensitivity and selectivity colorimetric and fluorescent detection for Hg2+ and efficient catalysis

    Science.gov (United States)

    Su, Dongyue; Yang, Xin; Xia, Qingdong; Zhang, Qi; Chai, Fang; Wang, Chungang; Qu, Fengyu

    2014-09-01

    In this research, folic acid functionalized silver nanoparticles (FA-AgNPs) were selected as a colorimetric and a ‘turn on’ fluorescent sensor for detecting Hg2+. After being added into Hg2+, AgNPs can emit stable fluorescence at 440 nm when the excitation wavelength is selected at 275 nm. The absorbance and fluorescence of the FA-AgNPs could reflect the concentration of the Hg2+ ions. Thus, we developed a simple, sensitive analytical method to detect Hg2+ based on the colorimetric and fluorescence enhancement of FA-AgNPs. The sensor exhibits two linear response ranges between absorbance and fluorescence intensity with Hg2+ concentration, respectively. Meanwhile, a detection limit of 1 nM is estimated based on the linear relationship between responses with a concentration of Hg2+. The high specificity of Hg2+ with FA-AgNPs interactions provided the excellent selectivity towards detecting Hg2+ over other metal ions (Pb2+, Mg2+, Zn2+, Ni2+, Cu2+, Co2+, Ca2+, Mn2+, Fe2+, Cd2+, Ba2+, Cr6+ and Cr3+). This will provide a simple, effective and multifunctional colorimetric and fluorescent sensor for on-site and real-time Hg2+ ion detection. The proposed method can be applied to the analysis of trace Hg2+ in lake water. Additionally, the FA-AgNPs can be used as efficient catalyst for the reduction of 4-nitrophenol and potassium hexacyanoferrate (III).

  7. Trace- and rare-earth element geochemistry and Pb-Pb dating of black shales and intercalated Ni-Mo-PGE-Au sulfide ores in Lower Cambrian strata, Yangtze Platform, South China

    Science.gov (United States)

    Jiang, Shao-Yong; Chen, Yong-Quan; Ling, Hong-Fei; Yang, Jing-Hong; Feng, Hong-Zhen; Ni, Pei

    2006-08-01

    The Lower Cambrian black shale sequence of the Niutitang Formation in the Yangtze Platform, South China, hosts an extreme metal-enriched sulfide ore bed that shows >10,000 times enrichment in Mo, Ni, Se, Re, Os, As, Hg, and Sb and >1,000 times enrichment in Ag, Au, Pt, and Pd, when compared to average upper continental crust. We report in this paper trace- and rare-earth-element concentrations and Pb-Pb isotope dating for the Ni-Mo-PGE-Au sulfide ores and their host black shales. Both the sulfide ores and their host black shales show similar trace-element distribution patterns with pronounced depletion in Th, Nb, Hf, Zr, and Ti, and extreme enrichment in U, Ni, Mo, and V compared to average upper crust. The high-field-strength elements, such as Zr, Hf, Nb, Ta, Sc, Th, rare-earth elements, Rb, and Ga, show significant inter-element correlations and may have been derived mainly from terrigenous sources. The redox sensitive elements, such as V, Ni, Mo, U, and Mn; base metals, such as Cu, Zn, and Pb; and Sr and Ba may have been derived from mixing of seawater and venting hydrothermal sources. The chondrite-normalized REE patterns, positive Eu and Y anomalies, and high Y/Ho ratios for the Ni-Mo-PGE-Au sulfide ores are also suggestive for their submarine hydrothermal-exhalative origin. A stepwise acid-leaching Pb-Pb isotope analytical technique has been employed for the Niutitang black shales and the Ni-Mo-PGE-Au sulfide ores, and two Pb-Pb isochron ages have been obtained for the black shales (531±24 Ma) and for the Ni-Mo-PGE-Au sulfide ores (521±54 Ma), respectively, which are identical and overlap within uncertainty, and are in good agreement with previously obtained ages for presumed age-equivalent strata.

  8. Removal and recovery of Hg(II) from aqueous solution using chitosan-coated cotton fibers.

    Science.gov (United States)

    Qu, Rongjun; Sun, Changmei; Ma, Fang; Zhang, Ying; Ji, Chunnuan; Xu, Qiang; Wang, Chunhua; Chen, Hou

    2009-08-15

    Two types of chitosan-coated cotton fibers (SCCH and RCCH) were applied to remove and recover Hg(II) ions in aqueous solution. The adsorption kinetics and isotherms of the two fibers for Hg(II) were investigated at different temperatures. The results revealed that the adsorption kinetic processes of SCCH and RCCH fibers for Hg(II) followed the pseudo second-order model at lower temperatures and the pseudo first-order model at higher temperatures. Both the Langmuir and Freundlich models well described the adsorption isotherms of SCCH and RCCH fibers for Hg(II) in the temperature range studied. SCCH and RCCH fibers selectively adsorbed Hg(II) from binary ion systems in the presence of Pb(II), Cu(II), Ni(II), Cd(II), Zn(II), Co(II), Mn(II) and Ag(I). Increased temperature was beneficial to adsorption. The recovery of Hg(II) from aqueous solutions was also studied as a function of sample flow rate and volume, concentration and volume of eluent, elution rate, quantity of adsorbents added and concomitant ions. The results showed that the two fibers efficiently enriched and recovered Hg(II) in the presence of alkali and alkaline earth metals and some heavy metals under optimum conditions. The RCCH fiber exhibited better stability than the SCCH fiber following repeated use.

  9. Measurement of the <mn>3mn>s>1mn>/>2mn>->3mn>p>3mn>/>2mn> resonance line of sodiumlike Eu<mn>52mn>+>

    Energy Technology Data Exchange (ETDEWEB)

    Träbert, E. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Beiersdorfer, P. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Hell, N. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Univ. of Erlangen-Nuremberg (Germany); Brown, G. V. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

    2015-08-01

    We have measured the 3 s 1 / 2 - 3 p 3 / 2 transition in sodiumlike Eu 52 + situated at 41.232 Å with an uncertainty of 73 ppm. Our measurement extends previous high-precision measurements into the 56 < Z < 78 range of atomic numbers. We also present measurements of 3 s 1 / 2 - 3 p 3 / 2 and 3 p 1 / 2 - 3 d 3 / 2 transitions in the neighboring magnesiumlike, aluminumlike, and siliconlike europium ions.

  10. Synthesis of undoped and manganese-doped hgte nanoparticles using [Hg(TeCH2CH2NMe2)2] as a single source precursor.

    Science.gov (United States)

    Kedarnath, Gotluru; Dey, Sandip; Jain, Vimal K; Dey, Gautam K; Kadam, Ramakant M

    2008-09-01

    The Reaction of [HgCl2(tmeda)] with NaTeCH2CH2NMe2 gave a mercury tellurolate, [Hg(TeCH2CH2. NMe2)2] (1) as a yellow crystalline solid, which was characterized by elemental analysis, UV-vis, mass and NMR (1H, 13C, 125Te, 199Hg) spectroscopy. Thermolysis of 1 in hexadecylamine (HDA) at 90 degrees C in the absence and presence of Mn(OAc)2.4H2O gave undoped and Mn-doped HgTe nanoparticles which were characterized by XRD, EDAX, TEM, EPR and magnetic measurements. These particles could be synthesized with mean particle size of 6-7 nm (from TEM). Manganese substitution at Hg site in HgTe lead to a linear decrease in lattice parameter with increasing concentration of Mn. Magnetization measurements showed ferromagnetic ordering at room temperature with very small coercive field (Hc, 50 Oe) for Hg0.973 Mn0.027 Te sample. This sample also exhibited distinct ferromagnetic resonance (FMR) in the EPR spectrum.

  11. Chemical stabilization and high pressure synthesis of Ba-free Hg-based superconductors, (Hg,M)Sr2Ca(n-1)Cu(n)O(y)(n=1 to approximately 3)

    Science.gov (United States)

    Kishio, K.; Shimoyama, J.; Hahakura, S.; Kitazawa, K.; Yamaura, K.; Hiroi, Z.; Takano, M.

    1995-01-01

    A homologous series of new Hg-based HTSC compounds, (Hg,M)Sr2Ca(n - 1)Cu(n)P(y) with n = 1 to 3, have been synthesized. The stabilization of the pure phases have been accomplished by chemical doping of third elements such as M = Cr, Mo and Re. While the Hgl2O1(n = 1) phase was readily obtained in this way, it was necessary to simultaneously dope Y into the Ca site to stabilize the Hg1212(n = 2) phase. On the other hand, single-phase Y-free Hg1212(n = 2) and Hg1223 (n = 3) samples were synthesized only under a high pressure of 6 GPa. In sharp contrast to the Ba containing compounds, all the samples prepared in the present study have been quite stable during the synthesis and no deterioration in air has been observed after the preparation.

  12. Hg transfer from contaminated soils to plants and animals

    NARCIS (Netherlands)

    Rodrigues, S.M.; Henriques, B.; Reis, A.T.; Duarte, A.C.; Pereira, E.; Romkens, P.F.A.M.

    2012-01-01

    Understanding the transfer of mercury (Hg) from soil to crops is crucial due to Hg toxicity and Hg occurrence in terrestrial systems. Previous research has shown that available Hg in soils contributes to plant Hg levels. Plant Hg concentrations are related to soil conditions and plant characteristic

  13. Study of the Zc<mo>+> channel using lattice QCD

    Energy Technology Data Exchange (ETDEWEB)

    Prelovsek, Sasa; Lang, C. B.; Leskovec, Luka; Mohler, Daniel

    2015-01-01

    Recently experimentalists have discovered several charged charmoniumlike hadrons Zcmo>+> with unconventional quark content cmo stretchy="false">¯mo>cdmo stretchy="false">¯mo>u. We perform a search for Zcmo>+> with mass below 4.2 GeV in the channel IGmo stretchy="false">(mo>JPCmo stretchy="false">)mo>mo>=>1mn>mo>+ stretchy="false">(mo>>1mn>mo>+mo>mo>- stretchy="false">)mo> using lattice QCD. The major challenge is presented by the two-meson states Jmo>/mo>ψπ, ψmn>2mn>Sπ, ψmn>1mn>D

  14. Microbial Oxidation of Hg(0) - Its Effect on Hg Stable Isotope Fractionation and Methylmercury Production

    Energy Technology Data Exchange (ETDEWEB)

    Yee, Nathan [Rutgers Univ., New Brunswick, NJ (United States); Barkay, Tamar [Rutgers Univ., New Brunswick, NJ (United States); Reinfelder, John [Rutgers Univ., New Brunswick, NJ (United States)

    2016-06-28

    Mercury (Hg) associated with mixed waste generated by nuclear weapons manufacturing has contaminated vast areas of the Oak Ridge Reservation (ORR). Neurotoxic methylmercury (MeHg) has been formed from the inorganic Hg wastes discharged into headwaters of East Fork Poplar Creek (EFPC). Thus, understanding the processes and mechanisms that lead to Hg methylation along the flow path of EFPC is critical to predicting the impacts of the contamination and the design of remedial action at the ORR. In part I of our project, we investigated Hg(0) oxidation and methylation by anaerobic bacteria. We discovered that the anaerobic bacterium Desulfovibrio desulfuricans ND132 can oxidize elemental mercury [Hg(0)]. When provided with dissolved elemental mercury, D. desulfuricans ND132 converts Hg(0) to Hg(II) and neurotoxic methylmercury [MeHg]. We also demonstrated that diverse species of subsurface bacteria oxidizes dissolved elemental mercury under anoxic conditions. The obligate anaerobic bacterium Geothrix fermentans H5, and the facultative anaerobic bacteria Shewanella oneidensis MR-1 and Cupriavidus metallidurans AE104 can oxidize Hg(0) to Hg(II) under anaerobic conditions. In part II of our project, we established anaerobic enrichment cultures and obtained new bacterial strains from the DOE Oak Ridge site. We isolated three new bacterial strains from subsurface sediments collected from Oak Ridge. These isolates are Bradyrhizobium sp. strain FRC01, Clostridium sp. strain FGH, and a novel Negativicutes strain RU4. Strain RU4 is a completely new genus and species of bacteria. We also demonstrated that syntrophic interactions between fermentative bacteria and sulfate-reducing bacteria in Oak Ridge saprolite mediate iron reduction via multiple mechanisms. Finally, we tested the impact of Hg on denitrification in nitrate reducing enrichment cultures derived from subsurface sediments from the Oak Ridge site, where nitrate is a major contaminant. We showed that there is an inverse

  15. Microbial Oxidation of Hg(0) - Its Effect on Hg Stable Isotope Fractionation and Methylmercury Production

    Energy Technology Data Exchange (ETDEWEB)

    Yee, Nathan [Rutgers Univ., New Brunswick, NJ (United States); Barkay, Tamar [Rutgers Univ., New Brunswick, NJ (United States); Reinfelder, John [Rutgers Univ., New Brunswick, NJ (United States)

    2016-06-28

    Mercury (Hg) associated with mixed waste generated by nuclear weapons manufacturing has contaminated vast areas of the Oak Ridge Reservation (ORR). Neurotoxic methylmercury (MeHg) has been formed from the inorganic Hg wastes discharged into headwaters of East Fork Poplar Creek (EFPC). Thus, understanding the processes and mechanisms that lead to Hg methylation along the flow path of EFPC is critical to predicting the impacts of the contamination and the design of remedial action at the ORR. In part I of our project, we investigated Hg(0) oxidation and methylation by anaerobic bacteria. We discovered that the anaerobic bacterium Desulfovibrio desulfuricans ND132 can oxidize elemental mercury [Hg(0)]. When provided with dissolved elemental mercury, D. desulfuricans ND132 converts Hg(0) to Hg(II) and neurotoxic methylmercury [MeHg]. We also demonstrated that diverse species of subsurface bacteria oxidizes dissolved elemental mercury under anoxic conditions. The obligate anaerobic bacterium Geothrix fermentans H5, and the facultative anaerobic bacteria Shewanella oneidensis MR-1 and Cupriavidus metallidurans AE104 can oxidize Hg(0) to Hg(II) under anaerobic conditions. In part II of our project, we established anaerobic enrichment cultures and obtained new bacterial strains from the DOE Oak Ridge site. We isolated three new bacterial strains from subsurface sediments collected from Oak Ridge. These isolates are Bradyrhizobium sp. strain FRC01, Clostridium sp. strain FGH, and a novel Negativicutes strain RU4. Strain RU4 is a completely new genus and species of bacteria. We also demonstrated that syntrophic interactions between fermentative bacteria and sulfate-reducing bacteria in Oak Ridge saprolite mediate iron reduction via multiple mechanisms. Finally, we tested the impact of Hg on denitrification in nitrate reducing enrichment cultures derived from subsurface sediments from the Oak Ridge site, where nitrate is a major contaminant. We showed that there is an inverse

  16. Developing low-cost carbon-based sorbents for Hg capture from flue gas

    Energy Technology Data Exchange (ETDEWEB)

    Ron Perry; Janos Lakatos; Colin E. Snape; Cheng-gong Sun [University of Nottingham (United Kingdom). UK Nottingham Fuel and Energy Centre, School of Chemical, Environmental and Mining Engineering

    2005-07-01

    To help reduce the cost of Hg capture, a number of low-cost carbons are being investigated, including tyre char, PFA carbons and gasification residues. This contribution reports the breakthrough capacities in fixed-bed screening tests for these materials in relation to those for commercial active carbons, including Norit FGD and the extent to which breakthrough capacities can be improved by MnO{sub 2} impregnation. 7 refs., 3 figs., 1 tab.

  17. [Heavy metals contents and Hg adsorption characteristics of mosses in virgin forest of Gongga Mountain].

    Science.gov (United States)

    Liang, Peng; Yang, Yong-Kui; He, Lei; Wang, Ding-Yong

    2008-06-01

    Seven main moss species in the Hailuogou virgin forest of Gongga Mountain were sampled to determine their heavy metals (Hg, Cr, Cd, Ni, Pb, Cu, Mn, Zn and Fe) content, and two widely distributed species, Pleurozium schreberi (Brid.) Mitt. and Racomitrium laetum Besch., were selected to study their Hg adsorption characteristics. The results showed that the heavy metals contents in the mosses were lower than the background values in Europe and America, except that the Cd had a comparable value, which indicated that the atmosphere in study area was not polluted by heavy metals and good in quality. The Hg adsorption by P. schreberi and R. laetum was an initiative and rapid process, with the equilibrium reached in about two hours, and could be well fitted by Freundlich and Langmuir equations. Based on Langmuir equation, the maximum Hg adsorption capacities of P. schreberi and R. laetum were 15.24 and 8.19 mg x g(-1), respectively, suggesting that the two mosses had a good capacity of Hg adsorption, and could be used as the bio-monitors of atmospheric Hg pollution.

  18. Simultaneous removal of Hg0 and HCN from the yellow phosphorus tail gas

    Science.gov (United States)

    Li, Yanan; Wang, Xueqian

    2017-08-01

    Transition metal oxides supported on TiO2 were synthesized by a sol-gel method and implied to simultaneous removal of Hg0 and HCN under low temperature and micro-oxygen conditions. The results show that catalysts that modified by manganese oxide have superior catalytic oxidation activity for both the removal of elemental mercury (Hg0) and HCN. Furthermore, the O2 can promote in the removal reaction process. The fresh and used catalysts were characterized by BET and XPS. The catalyst characterization indicated that the catalyst possessed a large specific surface area and the chemisorbed oxygen participated in the catalytic oxidation reaction. The MnOx/TiO2 catalyst was demonstrated to a good catalytic oxidant for simultaneous removal of elemental mercury (Hg0) and HCN under micro-oxygen conditions.

  19. "Naked-eye" colorimetric and "turn-on" fluorometric chemosensors for reversible Hg2+ detection.

    Science.gov (United States)

    Wanichacheva, Nantanit; Praikaew, Panida; Suwanich, Thanapat; Sukrat, Kanjarat

    2014-01-24

    Two new Hg(2+)-colorimetric and fluorescent sensors based on 2-[3-(2-aminoethylsulfanyl) propylsulfanyl]ethanamine covalently bound to one and two units of rhodamine-6G moieties, 1 and 2, were synthesised, and their sensing behaviors toward metal ions were investigated by UV/Vis and fluorescence spectroscopy. Upon the addition of Hg(2+), the sensors exhibited highly sensitive "turn-on" fluorescence enhancement as well as a color change from colorless to pink, which was readily noticeable for naked eye detection. Especially, 1 exhibited the reversible behavior and revealed a very high selectivity in the presence of competitive ions, particularly Cu(2+), Ag(+), Pb(2+), Ca(2+), Cd(2+), Co(2+), Fe(2+), Mn(2+), Na(+), Ni(2+), K(+), Ba(2+), Li(+) and Zn(2+), with a low detection limit of 1.7 ppb toward Hg(2+).

  20. High-Performance Corrosion-Resistant Iron-Based Amorphous Metals - The Effects of Composition, Structure and Environment: Fe49.7Cr17.7Mn1.9Mo7.4W1.6B15.2C3.8Si2.4

    Energy Technology Data Exchange (ETDEWEB)

    Farmer, J; Haslam, J; Day, S; Lian, T; Saw, C; Hailey, P; Choi, J; Yang, N; Bayles, R; Aprigliano, L; Payer, J; Perepezko, J; Hildal, K; Lavernia, E; Ajdelsztajn, L; Branagan, D J; Beardsely, M B

    2006-10-20

    Several Fe-based amorphous metal formulations have been identified that appear to have corrosion resistance comparable to (or better than) that of Ni-based Alloy C-22 (UNS No. N06022), based on measurements of breakdown potential and corrosion rate in seawater. Both chromium (Cr) and molybdenum (Mo) provide corrosion resistance, boron (B) enables glass formation, and rare earths such as yttrium (Y) lower critical cooling rate (CCR). SAM2X5 (Fe{sub 49.7}Cr{sub 17.7}Mn{sub 1.9}Mo{sub 7.4}W{sub 1.6}B{sub 15.2}C{sub 3.8}Si{sub 2.4}) has no yttrium, and is characterized by relatively high critical cooling rates of approximately 600 Kelvin per second. Data for the SAM2X5 formulation is reported here. In contrast to yttrium-containing iron-based amorphous metals, SAM2X5 can be readily gas atomized to produce spherical powders which enable more facile thermal spray deposition. The reference material, nickel-based Alloy C-22, is an outstanding corrosion-resistant engineering material. Even so, crevice corrosion has been observed with C-22 in hot sodium chloride environments without buffer or inhibitor. SAM2X5 also experiences crevice corrosion under sufficiently harsh conditions. Both Alloy C-22 and Type 316L stainless lose their resistance to corrosion during thermal spraying, due to the formation of deleterious intermetallic phases which depletes the matrix of key alloy elements, whereas SAM2X5 can be applied as coatings with the same corrosion resistance as a fully-dense completely amorphous melt-spun ribbon, provided that its amorphous nature is preserved during thermal spraying. The hardness of Type 316L Stainless Steel is approximately 150 VHN, that of Alloy C-22 is approximately 250 VHN, and that of HVOF SAM2X5 ranges from 1100-1300 VHN [MRS12-13]. Such hardness makes these materials particularly attractive for applications where corrosion-erosion and wear are also issues. Since SAM2X5 has high boron content, it can absorb neutrons efficiently, and may therefore find

  1. Removal of trace mercury(II) from aqueous solution by in situ formed Mn-Fe (hydr)oxides.

    Science.gov (United States)

    Lu, Xixin; Huangfu, Xiaoliu; Ma, Jun

    2014-09-15

    The efficiency and mechanism of trace mercury (Hg(II)) removal by in situ formed manganese-ferric (hydr)oxides (in situ Mn-Fe) were investigated by reacting KMnO4 with Fe(II) in simulated solutions and natural water. In the simulated solutions, the impact of coagulant dosage, pH, and temperature on mercury removal was studied. Experimental results showed that in situ Mn-Fe more effectively removed mercury compared with polyaluminum chloride (PAC) and iron(III) chloride (FeCl3), and that mercury existed in the form of uncharged species, namely Hg(OH)2, HgClOH(aq), and HgCl2(aq). Fourier transform infrared spectroscopy demonstrated that in situ Mn-Fe contained hydroxyl groups as the surface active sites, while X-ray photoelectron spectroscopy (XPS) measurements revealed that MnO2 or MnOOH and FeOOH were the dominant species in the precipitates. XPS analysis indicated that an Hg-Mn-Fe mixture was formed in the precipitates, suggesting that mercury was removed from solutions via transfer from the liquid phase to solid phase. These results indicated that the primary mercury removal mechanisms in in situ Mn-Fe were surface complexation and flocculation-precipitation processes. Satisfactory removal efficiency of mercury was also observed following in situ Mn-Fe in natural waters. Copyright © 2014 Elsevier B.V. All rights reserved.

  2. Elemental mercury oxidation and adsorption on magnesite powder modified by Mn at low temperature.

    Science.gov (United States)

    Xu, Yalin; Zhong, Qin; Liu, Xinya

    2015-01-01

    Mn modified the commercial magnesite powder prepared by wet impregnation method has been shown to be effective for gas-phase elemental mercury (Hg(0)) removal at low temperatures. The prepared samples are characterized in detail across multiform techniques: XRF, BET, SEM-EDX, XRD, H2-TPR, and XPS, and all the results show that the amorphous MnO2 impregnated on magnesite powder improves the removal efficiency of Hg(0). Through further analysis by TG and in situ FTIR, the reasonable removal mechanism is also speculated. The results indicate that chemisorbed oxygen is an important reactant in the heterogeneous reaction, and gas-phase Hg(0) is adsorbed and then oxidized to solid MnHgO3 on the surface of the adsorbent.

  3. /sup 203/Hg and other gamma-emitting radio-isotopes as labels for Dirofilaria immitis microfilariae

    Energy Technology Data Exchange (ETDEWEB)

    Lengemann, F.W.; Grieve, R.B.; Chmielewicz, M.; Georgi, J.R.

    1986-04-01

    The in vitro uptake of gamma-emitting radionuclides by microfilariae of Dirofilaria immitis was investigated. Radionuclides tested were /sup 133/Ba, /sup 207/Bi, /sup 82/Br, /sup 109/Cd, /sup 51/Cr, /sup 60/Co, /sup 59/Fe, /sup 203/Hg, /sup 125/I, /sup 54/Mn, /sup 32/P, /sup 125/Sb, /sup 46/Sc, /sup 75/Se and /sup 65/Zn. Only /sup 207/Bi, /sup 59/Fe, /sup 203/Hg, /sup 54/Mn and /sup 46/Sc showed more than 2% of the available radioactivity to bind to the microfilariae. When tested for retention in vitro only /sup 203/Hg showed retention levels approaching 90%. Moreover, when dimethyl-sulphoxide was incorporated into the medium at levels of 1% (v/v) the uptake of /sup 203/Hg could be increased by 3-5 times; no other radio-isotope tested responded in this manner. The uptake of /sup 203/Hg was directly related to temperature and time of incubation. Mercury, as mercuric chloride, was toxic to the microfilariae and represents an impediment to the incorporation of high levels of /sup 203/Hg in microfilariae.

  4. Induced polarization of Λ<mo>(>1116mn>)> in kaon electroproduction

    Energy Technology Data Exchange (ETDEWEB)

    Gabrielyan, M.; Raue, B. A.; Carman, D. S.; Park, K.; Adhikari, K. P.; Adikaram, D.; Amaryan, M. J.; Anefalos Pereira, S.; Avakian, H.; Ball, J.; Baltzell, N. A.; Battaglieri, M.; Baturin, V.; Bedlinskiy, I.; Biselli, A. S.; Bono, J.; Boiarinov, S.; Briscoe, W. J.; Brooks, W. K.; Burkert, V. D.; Cao, T.; Celentano, A.; Chandavar, S.; Charles, G.; Colaneri, L.; Cole, P. L.; Contalbrigo, M.; Cortes, O.; Crede, V.; D' Angelo, A.; Dashyan, N.; De Vita, R.; De Sanctis, E.; Deur, A.; Djalali, C.; Doughty, D.; Dupre, R.; El Fassi, L.; Eugenio, P.; Fedotov, G.; Fegan, S.; Fleming, J. A.; Forest, T. A.; Garillon, B.; Gevorgyan, N.; Ghandilyan, Y.; Gilfoyle, G. P.; Giovanetti, K. L.; Girod, F. X.; Goetz, J. T.; Golovatch, E.; Gothe, R. W.; Griffioen, K. A.; Guidal, M.; Guo, L.; Hafidi, K.; Hakobyan, H.; Hattawy, M.; Hicks, K.; Ho, D.; Holtrop, M.; Hughes, S. M.; Ilieva, Y.; Ireland, D. G.; Ishkhanov, B. S.; Jenkins, D.; Jiang, H.; Jo, H. S.; Joo, K.; Keller, D.; Khandaker, M.; Kim, W.; Klein, F. J.; Koirala, S.; Kubarovsky, V.; Kuhn, S. E.; Kuleshov, S. V.; Lenisa, P.; Levine, W. I.; Livingston, K.; MacGregor, I. J. D.; Mayer, M.; McKinnon, B.; Meyer, C. A.; Mestayer, M. D.; Mirazita, M.; Mokeev, V.; Moody, C. I.; Moutarde, H.; Movsisyan, A.; Munevar, E.; Munoz Camacho, C.; Nadel-Turonski, P.; Niccolai, S.; Niculescu, G.; Osipenko, M.; Pappalardo, L. L.; Paremuzyan, R.; Pasyuk, E.; Peng, P.; Phelps, W.; Phillips, J. J.; Pisano, S.; Pogorelko, O.; Pozdniakov, S.; Price, J. W.; Procureur, S.; Protopopescu, D.; Rimal, D.; Ripani, M.; Rizzo, A.; Sabatié, F.; Salgado, C.; Schott, D.; Schumacher, R. A.; Simonyan, A.; Smith, G. D.; Sober, D. I.; Sokhan, D.; Stepanyan, S. S.; Stepanyan, S.; Strakovsky, I. I.; Strauch, S.; Sytnik, V.; Tang, W.; Ungaro, M.; Vlassov, A. V.; Voskanyan, H.; Voutier, E.; Walford, N. K.; Watts, D. P.; Wei, X.; Weinstein, L. B.; Zachariou, N.; Zana, L.; Zhang, J.; Zonta, I.

    2014-09-01

    We have measured the induced polarization of the Λ(1116) in the reaction ep→e'K+Λ, detecting the scattered e' and K+ in the final state along with the proton from the decay Λ→pπ-.The present study used the CEBAF Large Acceptance Spectrometer (CLAS), which allowed for a large kinematic acceptance in invariant energy W (1.6≤W≤2.7 GeV) and covered the full range of the kaon production angle at an average momentum transfer Q2=1.90 GeV2.In this experiment a 5.50 GeV electron beam was incident upon an unpolarized liquid-hydrogen target. We have mapped out the W and kaon production angle dependencies of the induced polarization and found striking differences from photoproduction data over most of the kinematic range studied. However, we also found that the induced polarization is essentially Q2 independent in our kinematic domain, suggesting that somewhere below the Q2 covered here there must be a strong Q2 dependence. Along with previously published photo- and electroproduction cross sections and polarization observables, these data are needed for the development of models, such as effective field theories, and as input to coupled-channel analyses that can provide evidence of previously unobserved s-channel resonances.

  5. Mn-oxidizing Bacteria in Oak Ridge, TN and the Potential for Mercury Remediation

    Science.gov (United States)

    Wright, K. L.; McNeal, K. S.; Han, F. X.

    2012-12-01

    East Fork Poplar Creek (EFPC) in Oak Ridge, TN was highly contaminated with elemental mercury in the 1950 and 1960. The area is still experiencing the effects of mercury contamination, and researchers are searching for ways to remediate the EFPC. One possible mechanism for bioremediation is the use of biogenic Mn oxides to remove heavy metals from water systems. Six native Pseudomonas bacteria species were isolated from the EFPC in order to examine biogenic Mn oxides production and bioremediation of Oak Ridge slurries. To investigate the biochemical interactions of Pseudomonas and the native microbial communities with Hg, Mn, Fe, S, six different slurry treatment groups were compared using inductively coupled plasma-atomic emission spectrometry (ICP-AES) and cold vapor atomic absorption spectrometry (CVAAS). Oak Ridge slurries were autoclaved to inhibit microbial growth (group 1), autoclaved and amended with HgS (group 2), autoclaved and amended with Pseudomonas isolates and additional HgS (group 3), untreated slurry (group 4), normal slurry amended with HgS (group 5), and normal slurry amended with Pseudomonas isolates and additional HgS (group 6). The comparison of the autoclaved groups with the counterpart untreated and normal Oak Ridge slurries highlighted important microbial interactions. Also, the Pseudomonas isolates were grown separately in a MnSO4 media, and the individual bacteria were monitored for Mn-oxidization using ICP-AES and transmission electron microscopy (TEM). In the slurry sediments, the Pseudomonas isolates did produce Mn oxides which bound to mercury, and mercury bound to organic matter significantly decreased. However, after a significant decrease of dissolved mercury in the water, dissolved mercury was cycled back into the water system on day 10 of the study. Additionally, two individual native Oak Ridge Pseudomonas isolates demonstrated Mn-oxidization. Biogenic Mn oxides have the potential to decrease mercury cycling, however there is

  6. Properties of Superconducting Mo, Mo2n and Trilayer Mo2n-Mo-Mo2n Thin Films

    Science.gov (United States)

    Barrentine, E. M.; Stevenson, T. R.; Brown, A. D.; Lowitz, A. E.; Noroozian, O.; U-Yen, K.; Eshan, N.; Hsieh, W. T.; Moseley, S. H.; Wollack, E. J.

    2014-01-01

    We present measurements of the properties of thin film superconducting Mo, Mo2N and Mo2N/Mo/Mo2N trilayers of interest for microwave kinetic inductance detector (MKID) applications. Using microwave resonator devices, we investigate the transition temperature, energy gaps, kinetic inductance, and internal quality factors of these materials. We present an Usadel-based interpretation of the trilayer transition temperature as a function of trilayer thicknesses, and a 2-gap interpretation to understand the change in kinetic inductance and internal resonance quality factor (Q) as a function of temperature.

  7. Emission Spectra of Working Mixtures of a HgBr/HgCl Excimer Lamp

    Science.gov (United States)

    Malinin, A. N.; Guĭvan, N. N.; Shimon, L. L.

    2000-12-01

    A study of emission spectra of a gas-discharge plasma produced in a HgBr/HgCl excimer lamp, which is filled with multicomponent working mixtures at atmospheric pressure (HgBr2 and HgCl2 with additions of molecular nitrogen and xenon), are reported. A gas-discharge plasma was produced by high-frequency (pulses ˜100 ns long with a repetition rate of up to 2000 Hz) barrier and surface discharges, which took place simultaneously. Emission of HgBr* and HgCl* excimer molecules, the second positive system of molecular oxygen, and helium and xenon lines in the UV, visible, and IR spectral regions was observed. The strongest emission of HgBr* and HgCl* molecules (the emission intensities were in the ratio 10:1) was observed in the HgBr2: HgCl2: N2: He mixture. Regularities in spectral and integrated characteristics of gas-discharge plasma emission are discussed.

  8. HgTe-CdTe SUPERLATTICES

    OpenAIRE

    Smith, D; Mcgill, T.

    1984-01-01

    We report on a theoretical study of the electronic properties of HgTe-CdTe superlattices. The band gap as a function of layer thickness, effective masses normal to the layer plane and tunneling length are compared to the corresponding (Hg, Cd)Te alloys. We find that the superlattice possesses a number of properties that may make it superior to the corresponding alloy as an infrared material.

  9. Hg0 absorption in potassium persulfate solution

    Institute of Scientific and Technical Information of China (English)

    YE Qun-feng; WANG Cheng-yun; WANG Da-hui; SUN Guan; XU Xin-hua

    2006-01-01

    The aqueous phase oxidation of gaseous elemental mercury (Hg0) by potassium persulfate (KPS) catalyzed by Ag+was investigated using a glass bubble column reactor. Concentration of gaseous mercury and potassium persulfate were measured by cold vapor atom absorption (CVAA) and ion chromatograph (IC), respectively. The effects of pH value, concentration of potassium persulfate and silver nitrate (SN), temperature, Hg0 concentration in the reactor inlet and tertiary butanol (TBA), free radical scavenger, on the removal efficiency of Hg0 were studied. The results showed that the removal efficiency of Hg0 increased with increasing concentration of potassium persulfate and silver nitrate, while temperature and TBA were negatively effective. Furthermore, the removal efficiency of Hg0 was much better in neutral solution than in both acidic and alkaline solution. But the influence of pH was almost eliminated by adding AgNO3. High Hg0 concentration has positive effect. The possible reaction mechanism of gaseous mercury was also discussed.

  10. 46 CFR 53.05-1 - Safety valve requirements for steam boilers (modifies HG-400 and HG-401).

    Science.gov (United States)

    2010-10-01

    ... 46 Shipping 2 2010-10-01 2010-10-01 false Safety valve requirements for steam boilers (modifies HG... requirements for steam boilers (modifies HG-400 and HG-401). (a) The pressure relief valve requirements and the safety valve requirements for steam boilers must be as indicated in HG-400 and HG-401 of section IV...

  11. Investigation of Hg uptake and transport between paddy soil and rice seeds combining Hg isotopic composition and speciation

    Directory of Open Access Journals (Sweden)

    C. Feng

    2016-02-01

    Full Text Available Abstract Human consumption of rice constitutes a potential toxicological risk in mercury (Hg polluted areas such as Hg mining regions in China. It is recognized to be an important source of Hg for the local human diet considering the efficient bioaccumulation of methylmercury (MeHg in rice seed. To assess Hg sources and uptake pathways to the rice plants, Hg speciation and isotopic composition were investigated in rice seeds and their corresponding paddy soils from different locations within the Wanshan Hg mining area (Guizhou Province, China. A large variation of Hg speciation is observed in rice seeds and paddy soils irrespective of the sampling location. Mass dependent fractionation (MDF of Hg in rice seeds differs by up to ∼4.0 ‰ in δ202Hg values, while mass independent fractionation (MIF of Hg isotopes remains constant (Δ199Hg ∼ 0‰. Hg isotopic composition in rice seeds covaries with that of paddy soils but exhibits lighter isotopic signature (δ202Hg. Such isotopic offset is mainly attributed to plant uptake and translocation processes. Also, seeds containing higher MeHg (MeHg/total Hg > 50% have significantly heavier Hg isotopes suggesting that MeHg uptake and transport to the seed in such rice plants is facilitated compared to inorganic Hg.

  12. Long-term Hg pollution induced Hg tolerance in the terrestrial isopod Porcellio scaber (Isopoda, Crustacea).

    Science.gov (United States)

    Lapanje, A; Drobne, D; Nolde, N; Valant, J; Muscet, B; Leser, V; Rupnik, M

    2008-06-01

    The aim of our work was to assess the pollution-induced community tolerance (PICT) of isopod gut microbiota and pollution-induced isopod population tolerance (PIPT). Animals collected from a chronically Hg polluted and an unpolluted location were exposed for 14 days to 10microg Hg/g dry food under laboratory conditions. The lysosomal membrane stability, hepatopancreas epithelium thickness, feeding activity and animal bacterial gut microbiota composition were determined. The results confirm the hypothesis that the response to short-term Hg exposure differs for animals from the Hg polluted and the unpolluted field locations. The animals and their gut microbiota from the Hg polluted location were less affected by Hg in a short-term feeding experiment than those from the unpolluted environment. We discuss the pollution-induced population tolerance of isopods and their gut microbiota as a measure of effects of long-term environmental pollution. The ecological consequences of such phenomena are also discussed.

  13. Zuotai and HgS differ from HgCl2 and methyl mercury in Hg accumulation and toxicity in weanling and aged rats.

    Science.gov (United States)

    Zhang, Bin-Bin; Li, Wen-Kai; Hou, Wei-Yu; Luo, Ya; Shi, Jing-Zhen; Li, Cen; Wei, Li-Xin; Liu, Jie

    2017-09-15

    Mercury sulfides are used in Ayurvedic medicines, Tibetan medicines, and Chinese medicines for thousands of years and are still used today. Cinnabar (α-HgS) and metacinnabar (β-HgS) are different from mercury chloride (HgCl2) and methylmercury (MeHg) in their disposition and toxicity. Whether such scenario applies to weanling and aged animals is not known. To address this question, weanling (21d) and aged (450d) rats were orally given Zuotai (54% β-HgS, 30mg/kg), HgS (α-HgS, 30mg/kg), HgCl2 (34.6mg/kg), or MeHg (MeHgCl, 3.2mg/kg) for 7days. Accumulation of Hg in kidney and liver, and the toxicity-sensitive gene expressions were examined. Animal body weight gain was decreased by HgCl2 and to a lesser extent by MeHg, but unaltered after Zuotai and HgS. HgCl2 and MeHg produced dramatic tissue Hg accumulation, increased kidney (kim-1 and Ngal) and liver (Ho-1) injury-sensitive gene expressions, but such changes are absent or mild after Zuotai and HgS. Aged rats were more susceptible than weanling rats to Hg toxicity. To examine roles of transporters in Hg accumulation, transporter gene expressions were examined. The expression of renal uptake transporters Oat1, Oct2, and Oatp4c1 and hepatic Oatp2 was decreased, while the expression of renal efflux transporter Mrp2, Mrp4 and Mdr1b was increased following HgCl2 and MeHg, but unaffected by Zuotai and HgS. Thus, Zuotai and HgS differ from HgCl2 and MeHg in producing tissue Hg accumulation and toxicity, and aged rats are more susceptible than weanling rats. Transporter expression could be adaptive means to reduce tissue Hg burden. Copyright © 2017 Elsevier Inc. All rights reserved.

  14. Syntheses and Crystal Structure of [Cu(pyr)3]·Hg2I6

    Institute of Scientific and Technical Information of China (English)

    宋俊玲; 曾卉一; 杨冰苹; 董振超; 郭国聪; 黄锦顺

    2003-01-01

    A new compound containing discrete cationic and anionic complexes, [Cu(pyr)3](Hg2I6 (C30H24CuHg2I6N6), where pyr = 2,2'-bipyridine, was prepared by the reaction of CuBr with pyr and HgI2 in a mixed solvent of acetone, methanol and acetonitrile. Single-crystal X-ray diffraction analysis indicates that it crystallizes in an orthorhombic system, Pna21 (No. 33), a = 33.1595(7), b = 9.4605(1), c = 13.0899(2) A。, V = 4106.4(1) A。3, Mr = 1694.67, Dc = 2.741 g/cm3, Z = 4, F(000) = 3012, μ(MoKα) = 12.511 mm-1, R = 0.0736, wR = 0.1360 (I > 2σ(I)) and S = 1.218. The structure consists of discrete [Hg2I6]2- anions and [Cu(bipyridine)3]2+ cations. The double tetrahedral [Hg2I6]2- unit is formed by sharing one tetrahedral edge and possesses approximate D2h symmetry. The mononuclear Cu2+ ion is coordinated by six N atoms from three pyr molecules to form a slightly disordered octahedral geometry.

  15. Local probing of Hg neighboorhood in HgBa$_{2}$CuO$_{4+\\delta}$

    CERN Document Server

    Correia, J G; Loureiro, S M; Toulemonde, P; Le Floc'h, S; Bordet, P; Capponi, J J; Gatt, R; Tröger, W; Ctortecka, B; Butz, T; Haas, H; Marques, J G; Soares, J C

    2000-01-01

    Electric field gradients (EFG) on mercury sites of the Hg1201 high-TC superconductors were measured with the perturbed angular correlation (PAC) technique. In Hg1201 samples where PAC detects higher oxygen content the EFGs have decreased to lower values indicating an elongation of the Hg-apical oxygen dumb-bell. On the same samples the asymmetry parameter of the EFG becomes non-zero below 100 K, showing that the charge distribution near the Hg-apical oxygen chain becomes non-axially symmetric at low temperature.

  16. Complexation of Hg with phytochelatins is important for plant Hg tolerance.

    Science.gov (United States)

    Carrasco-Gil, Sandra; Alvarez-Fernández, Ana; Sobrino-Plata, Juan; Millán, Rocío; Carpena-Ruiz, Ramón O; Leduc, Danika L; Andrews, Joy C; Abadía, Javier; Hernández, Luís E

    2011-05-01

    Three-week-old alfalfa (Medicago sativa), barley (Hordeum vulgare) and maize (Zea mays) were exposed for 7 d to 30 µm of mercury (HgCl(2) ) to characterize the Hg speciation in root, with no symptoms of being poisoned. The largest pool (99%) was associated with the particulate fraction, whereas the soluble fraction (SF) accounted for a minor proportion (phytochelatins (PCs) in root SF, which was particularly varied in alfalfa (eight ligands and five stoichiometries), a species that also accumulated homophytochelatins. Spatial localization of Hg in alfalfa roots by microprobe synchrotron X-ray fluorescence spectroscopy showed that most of the Hg co-localized with sulphur in the vascular cylinder. Extended X-ray Absorption Fine Structure (EXAFS) fingerprint fitting revealed that Hg was bound in vivo to organic-S compounds, i.e. biomolecules containing cysteine. Albeit a minor proportion of total Hg, Hg-PCs complexes in the SF might be important for tolerance to Hg, as was found with Arabidopsis thaliana mutants cad2-1 (with low glutathione content) and cad1-3 (unable to synthesize PCs) in comparison with wild type plants. Interestingly, high-performance liquid chromatography-electrospray ionization-time of flight analysis showed that none of these mutants accumulated Hg-biothiol complexes.

  17. Structures of Mn clusters

    Indian Academy of Sciences (India)

    Tina M Briere; Marcel H F Sluiter; Vijay Kumar; Yoshiyuki Kawazoe

    2003-01-01

    The geometries of several Mn clusters in the size range Mn13–Mn23 are studied via the generalized gradient approximation to density functional theory. For the 13- and 19-atom clusters, the icosahedral structures are found to be most stable, while for the 15-atom cluster, the bcc structure is more favoured. The clusters show ferrimagnetic spin configurations.

  18. Removal of Hg{sup 0} from flue gases in wet FGD by catalytic oxidation with air - An experimental study

    Energy Technology Data Exchange (ETDEWEB)

    Andrej Stergarsek; Milena Horvat; Peter Frkal; Jost Stergarsek [' Jozef Stefan' Institute, Ljubljana (Slovenia)

    2010-11-15

    Research efforts are being focused on the development of mercury removal technologies, mainly directed to two alternative approaches: (I) the enhancement of homogeneous oxidation in the flue gases of Hg{sup 0} to water soluble Hg{sup 2+} by the addition of chlorides or bromides to the boiler or; (ii) the adsorption of Hg{sup 2+} and Hg{sup 0} on impregnated activated carbon (AC). A third option gaining more attention lately is based on the oxidation and retention of dissolved Hg{sup 0} in the wet flue gas desulphurisation (FGD) system. The experimental evidence of the present work showed that Hg{sup 0} present in the gaseous phase can be dissolved and oxidized to a high degree (70-90%) by air together with SO{sub 3}{sup 2-} in wet FGD solutions. Transition metals such as Fe{sup 2+} and Mn{sup 2+} act as catalysts, chloride enhances the reaction, while some oxosulphur compounds, e.g. tetrathionate, inhibit the oxidation. A combination of several catalysts at a concentration of sulphite (SO{sub 3}{sup 2-}) below 100 mg L{sup -1} and an adequate redox potential of the solution can assure reasonable mercury removal even in the presence of oxidation inhibiting compounds. The main competitive reactions that govern final Hg{sup 0} removal in the FGD are as follows: (1) oxidation of Hg{sup 0} together with SO{sub 2} with air, enhanced by catalysts; (2) removal of catalysts by precipitation in the form of Fe(OH){sub 3} and eventually as MnO{sub 2} (to overcome this problem continuous addition of catalysts to the solution is required); (3) reduction of Fe{sup 3+} by tetrathionate to Fe{sup 2+} which (4) may reduce Hg{sup 2+} to Hg{sup 0} and probably (5) the complexation of Hg{sup 2+} by anions present which may play an important role in the mechanism by complexing the product(s) of the Hg{sup 0} oxidation reaction. 35 refs., 10 figs., 7 tabs.

  19. HgCdTe barrier infrared detectors

    Science.gov (United States)

    Kopytko, M.; Rogalski, A.

    2016-05-01

    In the last decade, new strategies to achieve high-operating temperature (HOT) detectors have been proposed, including barrier structures such as nBn devices, unipolar barrier photodiodes, and multistage (cascade) infrared detectors. The ability to tune the positions of the conduction and valence band edges independently in a broken-gap type-II superlattices is especially helpful in the design of unipolar barriers. This idea has been also implemented in HgCdTe ternary material system. However, the implementation of this detector structure in HgCdTe material system is not straightforward due to the existence of a valence band discontinuity (barrier) at the absorber-barrier interface. In this paper we present status of HgCdTe barrier detectors with emphasis on technological progress in fabrication of MOCVD-grown HgCdTe barrier detectors achieved recently at the Institute of Applied Physics, Military University of Technology. Their performance is comparable with state-of-the-art of HgCdTe photodiodes. From the perspective of device fabrication their important technological advantage results from less stringent surface passivation requirements and tolerance to threading dislocations.

  20. Possible martensitic transformation and ferrimagnetic properties in Heusler alloy Mn{sub 2}NiSn

    Energy Technology Data Exchange (ETDEWEB)

    Duan, Ying-Ni, E-mail: duanyingni@163.com [Department of Medical Engineering and Technology, Xinjiang Medical University, Urumqi 830011, Xinjiang (China); Fan, Xiao-Xi; Kutluk, Abdugheni [Department of Medical Engineering and Technology, Xinjiang Medical University, Urumqi 830011, Xinjiang (China); Du, Xiu-Juan [School of Applied Science, Taiyuan University of Science and Technology, Taiyuan 030024, Shanxi (China); Zhang, Zheng-Wei [Chemistry and Chemical Engineering Laboratory, The Xinjiang Technical Institute of Physics & Chemistry, Chinese Academy of Sciences, Urumqi 830011, Xinjiang (China); Song, Yu-Ling [College of Physics and Electronic Engineering, Nanyang Normal University, Nanyang 473061, Henan (China)

    2015-07-15

    The electronic structure and magnetic properties of Hg{sub 2}CuTi-type Mn{sub 2}NiSn have been studied by performing the first-principle calculations. It is found that the phase transformation from the cubic to the tetragonal structure reduces the total energy, indicating that the martensitic phase is more stable and the phase transition from austenite to martensite may happen at low temperature for Hg{sub 2}CuTi-type Mn{sub 2}NiSn. Concerning the magnetism of Hg{sub 2}CuTi-type Mn{sub 2}NiSn, both austenitic and martensitic phases are suggested to be ferrimagnets. Furthermore, martensitic transformation decreases the magnetic moment per formula unit compared with austenitic phase. The results are helpful to accelerate the use of Mn{sub 2}NiSn alloys in the series for magnetic shape memory applications. - Highlights: • It is found that the phase transition from austenite to martensite may happen at low temperature for Mn{sub 2}NiSn with the Hg{sub 2}CuTi-type structure. • Both austenitic and martensitic Mn{sub 2}NiSn are ferrimagnets. • Martensitic transformation decreases the magnetization.

  1. High performance Mo adsorbent PZC

    Energy Technology Data Exchange (ETDEWEB)

    Anon.

    1998-10-01

    We have developed Mo adsorbents for natural Mo(n, {gamma}){sup 99}Mo-{sup 99m}Tc generator. Among them, we called the highest performance adsorbent PZC that could adsorb about 250 mg-Mo/g. In this report, we will show the structure, adsorption mechanism of Mo, and the other useful properties of PZC when you carry out the examination of Mo adsorption and elution of {sup 99m}Tc. (author)

  2. Properties of Zr-Ti-V-Mn-Ni hydride alloy

    Institute of Scientific and Technical Information of China (English)

    文明芬; 翟玉春; 王新海; 陈廉

    2002-01-01

    Six kinds of Zr-based hydride alloy were designed. XRD analyses show that the main phase of Zr1-xTix-(NiCoMnV)2.1 alloy is Laves C15 when x is between 0 and 0.5,but the more the content of Ti, the more the Laves C14 phases. The amount of Laves C14 can be up to the amount of Laves C15 after substituted V and Fe by V-Fe alloy in Zr0.6-Ti0.4(NiCoMnVFeCr)1.7 alloy. The electrochemical measurements show that the discharge capacity of Zr0.9Ti0.1-(NiCoMnV)2.1 electrode is about 340mA * h/g at 60mA/g, but with increasing the amount of Ti, the discharge capacity of alloy electrode abruptly decreases; at 300mA/g current density, its Kr can be up to 91%. The discharge capacity of Zr0.6-Ti0.4-(NiCoMn(V-Fe)Cr)1.62 alloy electrode is about 200mA * h/g at first cycle, the maximum capacity is more than that of the electrode with pure V, and about 315mA * h/g.

  3. Complexation of Hg with phytochelatins is important for plant Hg tolerance

    National Research Council Canada - National Science Library

    CARRASCO‐GIL, SANDRA; ÁLVAREZ‐FERNÁNDEZ, ANA; SOBRINO‐PLATA, JUAN; MILLÁN, ROCÍO; CARPENA‐RUIZ, RAMÓN O; LEDUC, DANIKA L; ANDREWS, JOY C; ABADÍA, JAVIER; HERNÁNDEZ, LUÍS E

    2011-01-01

    Three‐week‐old alfalfa ( Medicago sativa ), barley ( Hordeum vulgare ) and maize ( Zea mays ) were exposed for 7 d to 30  µ m of mercury (HgCl 2 ) to characterize the Hg speciation in root, with no symptoms of being poisoned...

  4. Temporal Characteristics of Emission of Working Mixtures of a HgBr/HgCl Excimer Lamp

    Science.gov (United States)

    Malinin, A. N.; Guĭvan, N. N.; Shimon, L. L.; Polyak, A. V.; Zubrilin, N. G.; Shchedrin, A. I.

    2001-12-01

    Results of a study of temporal characteristics of the emission of gas-discharge plasma of atmospheric pressure in multicomponent mixtures (mercury dibromide and dichloride with helium and additions of molecular nitrogen and xenon) of working media of HgBr/HgCl excimer lamps are presented. Gas-discharge plasma was produced and components of the working mixture were excited by high-frequency barrier and surface discharges occurring simultaneously. The repetition rate of the pumping pulse and its duration are 1000 Hz and ˜100 ns, respectively. It is found that the amplitude and the length of emission pulses and their trailing edge are modified in HgBr2: HgCl2: Xe: He and HgBr2: HgCl2: N2: He mixtures when xenon and molecular nitrogen are added, as compared to a HgBr2: HgCl2: He mixture. Regularities observed in temporal characteristics of gas-discharge plasma emission are discussed.

  5. Ground-state potential energy curves of LiHg, NaHg, and KHg revisited

    Science.gov (United States)

    Thiel, Linda; Hotop, Hartmut; Meyer, Wilfried

    2003-11-01

    We present the results of large-scale CCSD(T) calculations on the potential energy curves for the ground states of LiHg, NaHg, and KHg. In these calculations, the Hg20+ core is simulated by a pseudopotential which has been adjusted to reproduce experimental excitation and ionization energies of the Hg atom at the coupled-cluster level. Moreover, we apply a weighted multiproperty fitting procedure to determine reliable potentials for LiHg, NaHg, and KHg which reproduce the available experimental results. In the case of LiHg, this best-fit potential is based solely on experimental data and its agreement with our calculated potential supports our computational procedure. For NaHg and KHg the experimental data had to be complemented by theoretical results in order to fix a best-fit potential. Our potentials and those proposed previously are evaluated by comparing calculated scattering cross sections and vibrational energy levels with the available experimental data.

  6. Cr, Cu, Mn, Mo, Ni, and Steel Price Drivers

    Science.gov (United States)

    Papp, John F.; Corathers, Lisa A.; Edelstein, Daniel L.; Fenton, Michael D.; Kuck, Peter H.; Magyar, Michael J.

    2007-01-01

    Summary This report contains the 55 slide images from a presentation made by the author at the meeting of the Metal Powder Industries Federation held in Denver, CO, on May 15, 2007. The Metal Powder Industries Federation (MPIF) invited the U.S. Geological Survey (USGS) to speak at their annual meeting about the price drivers for chromium, copper, manganese, molybdenum, nickel, and steel. These metals are of interest to MPIF because the prices of these raw materials used by their industry were at historically high levels. Because the USGS closely monitors, yet neither buys nor sells, metal commodities, it is an unbiased source of metal price information and analysis. The authors used information about these and other metals collected and published by the USGS (U.S. production, trade, stocks, and prices) and about consumption and stocks internationally by country from industry organizations that publish such information, because metal markets are influenced by activities and events over the entire globe. By seeking a common cause for common behavior among the various metal commodities, the authors found that major price drivers on metal commodities were inflation, major international events such as wars and recessions, and major national events such as the dissolution of the Soviet Union in 1991 and economic growth in China, which started with the open door policy in the 1970s but did not have significant market impact until starting in the 1990s. Metal commodity prices also responded to commodity-specific events.

  7. Quasiparticle excitations in superdeformed {sup 192}Hg

    Energy Technology Data Exchange (ETDEWEB)

    Lauritsen, T.; Carpenter, M.P.; Janssens, R.V.F. [and others

    1995-08-01

    The nucleus {sup 192}Hg plays a pivotal role for superdeformation in the mass 190 region, since calculations of single-particle levels show large shell-gaps for the superdeformed (SD) shape at N = 112 and Z = 80. As a result, {sup 192}Hg is referred to as the doubly magic SD nucleus for the A = 190 region. In previous studies, only one superdeformed band was observed in this nucleus, and this fact was cited as indirect evidence that large shell gaps do indeed exist at the proposed particle numbers.

  8. Electric field gradients in Hg compounds

    DEFF Research Database (Denmark)

    Arcisauskaité, Vaida; Knecht, Stefan; Sauer, Stephan P. A.

    2012-01-01

    We examine the performance of Density Functional Theory (DFT) approaches based on the Zeroth-Order Regular Approximation (ZORA) Hamiltonian (with and without inclusion of spinorbit coupling) for predictions of electric ¿eld gradients (EFGs) at the heavy atom Hg nucleus. This is achieved by compar......We examine the performance of Density Functional Theory (DFT) approaches based on the Zeroth-Order Regular Approximation (ZORA) Hamiltonian (with and without inclusion of spinorbit coupling) for predictions of electric ¿eld gradients (EFGs) at the heavy atom Hg nucleus. This is achieved...

  9. Doping induced modification in polyhedral tilt in hexagonal Ho1-xYxMnO3

    Science.gov (United States)

    Kaushik, S. D.; Rayaprol, S.

    2012-06-01

    We have studied the effect of systematic doping of Y at Ho site on the crystal structure of hexagonal HoMnO3 We have carried out room temperature neutron diffraction (ND) study on Ho1-xYxMnO3 (x = 0, 0.25, 0.50, 0.75), and by analyzing this ND data we have determined the cell parameters, Mn-O bond length, O-Mn-O bond angle. The variation in certain M-O bond length and O-Mn-O bond angles has been understood in terms of modifications in tilt of the MnO5 polyhedra due to Ho site Y doping in hexagonal HoMnO3.

  10. Hg and As Minerals in Fluid Inclusions from the Williams Mine,Hemlo,and Their Genetic Implications

    Institute of Scientific and Technical Information of China (English)

    卢焕章; ANDDON.C.HARRIS

    2002-01-01

    The Hemlo mineralization is enigmatic compared to general Archean lode gold deposits based on the fact that is characterized by an exotic mineralogy containing elements such as As,Hg,Sb,Ba,V and Mo.The genetic concepts range from syngenetc to epigenetic types of mineralization.This reconnaissance study was designed to examine the relationshp of Hg-As minerals with respect of fluid inclusions in the Williams mine(formerly known as the Page Williams mine)covering the A and C ore zones.

  11. MoS₂ decoration by Mo-atoms and the MoS₂-Mo-graphene heterostructure: a theoretical study.

    Science.gov (United States)

    Kvashnin, D G; Sorokin, P B; Seifert, G; Chernozatonskii, L A

    2015-11-21

    Here we propose a completely new covalent heterostructure based on graphene and self-decorated MoS2 monolayers. Detailed investigation of the decoration process of the MoS2 surface by Mo adatoms was performed using first principles DFT methods. Comparison between valence-only and semicore pseudopotentials was performed to correctly describe the interaction between Mo adatoms and the MoS2 surface. It was found that self-decoration by Mo atoms is favorable from an energetic point of view. We studied in detail various decoration paths of Mo atoms on the MoS2 surface. The strong variation of electronic properties after the decoration of MoS2 was found. The impact of the presence of Mo adatoms on the electronic properties of the graphene/MoS2 heterostructure was shown.

  12. Growing rice aerobically markedly decreases mercury accumulation by reducing both Hg bioavailability and the production of MeHg.

    Science.gov (United States)

    Wang, Xun; Ye, Zhihong; Li, Bing; Huang, Linan; Meng, Mei; Shi, Jianbo; Jiang, Guibin

    2014-01-01

    Rice consumption represents a major route of mercury (Hg) and methylmercury (MeHg) exposure for those living in certain areas of inland China. In this study we investigated the effects of water management on bioavailable Hg, MeHg, and sulfate-reducing bacteria (SRB, abundance and community composition) in rhizosphere soil, and total Hg (THg) and MeHg in rice plants grown under glasshouse and paddy field conditions. Aerobic conditions greatly decreased the amount of THg and MeHg taken up by rice plants and affected their distribution in different plant tissues. There were positive correlations between bioavailable Hg and THg in brown rice and roots and between numbers of SRB and MeHg in brown rice, roots, and rhizosphere soil. Furthermore, the community composition of SRB was dramatically influenced by the water management regimes. Our results demonstrate that the greatly reduced bioavailability of Hg and production of MeHg are due to decreased SRB numbers and proportion of Hg methylators in the rhizosphere under aerobic conditions. These are the main reasons for the reduced Hg and MeHg accumulation in aerobically grown rice. Water management is indicated as an effective measure that can be used to reduce Hg and MeHg uptake by rice plants from Hg-contaminated paddy fields.

  13. 40 CFR 60.45Da - Standard for mercury (Hg).

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for mercury (Hg). 60.45Da... for mercury (Hg). (a) For each coal-fired electric utility steam generating unit other than an IGCC... gases that contain mercury (Hg) emissions in excess of each Hg emissions limit in paragraphs...

  14. MBE Growth and Characterization of Hg Based Compounds and Heterostructures

    Science.gov (United States)

    2002-06-03

    The molecular beam epitaxy ( MBE ) growth of Mercury Cadmium Telluride (Hg(1-x)Cd(x)Te) alloys and type III HgTe/Hg(1-x)Cd(x)Te heterostructures has...been discussed, including similarities and differences between the (0 0 1) and (1 1 2)Beta orientations. Furthermore, the MBE growth of HgTe-based

  15. Phenylselenolate Mercury Alkyl Compounds, PhSeHgMe and PhSeHgEt: Molecular Structures, Protolytic Hg-C Bond Cleavage and Phenylselenolate Exchange.

    Science.gov (United States)

    Yurkerwich, Kevin; Quinlivan, Patrick J; Rong, Yi; Parkin, Gerard

    2016-01-08

    The phenylselenolate mercury alkyl compounds, PhSeHgMe and PhSeHgEt, have been structurally characterized by X-ray diffraction, thereby demonstrating that both compounds are monomeric with approximately linear coordination geometries; the mercury centers do, nevertheless, exhibit secondary Hg•••Se intermolecular interactions that serve to increase the coordination number in the solid state. The ethyl derivative, PhSeHgEt, undergoes facile protolytic cleavage of the Hg-C bond to release ethane at room temperature, whereas PhSeHgMe exhibits little reactivity under similar conditions. Interestingly, the cleavage of the Hg-C bond of PhSeHgEt is also more facile than that of the thiolate analogue, PhSHgEt, which demonstrates that coordination by selenium promotes protolytic cleavage of the mercury-carbon bond. The phenylselenolate compounds PhSeHgR (R = Me, Et) also undergo degenerate exchange reactions with, for example, PhSHgR and RHgCl. In each case, the alkyl groups preserve coupling to the (199)Hg nuclei, thereby indicating that the exchange process involves metathesis of the Hg-SePh/Hg-X groups rather than metathesis of the Hg-R/Hg-R groups.

  16. The application of 199Hg NMR and 199mHg perturbed angular correlation (PAC) spectroscopy to define the biological chemistry of HgII

    DEFF Research Database (Denmark)

    Iranzo, Olga; Thulstrup, Peter Waaben; Ryu, Seung-baek;

    2007-01-01

    H values and at peptide/HgII ratios of 3:1 with an unusual trigonal thiolate coordination mode. The resulting HgII complexes are good water-soluble models for HgII binding to the protein MerR. We have carried out a parallel study using 199Hg NMR and 199mHg perturbed angular correlation (PAC) spectroscopy...... to characterize the distinct species that are generated under different pH conditions and peptide TRI L9C/HgII ratios. These studies prove for the first time the formation of [Hg{(TRI L9C)2-(TRI L9C H)}], a dithiolate-HgII complex in the hydrophobic interior of the three-stranded coiled coil (TRI L9C)3. 199Hg NMR...... and 199mHg PAC data demonstrate that this dithiolate-HgII complex is different from the dithiolate [Hg(TRI L9C)2], and that the presence of third -helix, containing a protonated cysteine, breaks the symmetry of the coordination environment present in the complex [Hg(TRI L9C)2]. As the pH is raised...

  17. Enhanced rate performance of molybdenum-doped spinel LiNi0.5Mn1.5O4 cathode materials for lithium ion battery

    Science.gov (United States)

    Yi, Ting-Feng; Chen, Bin; Zhu, Yan-Rong; Li, Xiao-Ya; Zhu, Rong-Sun

    2014-02-01

    The Mo-doped LiNi0.5Mn1.5O4 cathodes are successfully synthesized by citric acid-assisted sol-gel method. The result demonstrates that the Mo-doped LiMn1.4Ni0.55Mo0.05O4 cathodes present the improved electrochemical performance over pristine LiNi0.5Mn1.5O4. At the 2 C rate after 80 cycles, the discharge capacities are 68.5 mAh g-1 for the pristine LiNi0.5Mn1.5O4 material (53.9% of the capacity at 0.1 C), 107.4 mAh g-1 for the LiMn1.425Ni0.5Mo0.05O4 material (82.1% at 0.1 C), and 122.7 mAh g-1 for the LiMn1.4Ni0.55Mo0.05O4 material (90.5% at 0.1 C). Mo-doping is favorable for reducing the electrode polarization, suggesting that Mo-doped LiNi0.5Mn1.5O4 electrodes have faster lithium insertion/extraction kinetics during cycling. Mo-doped LiNi0.5Mn1.5O4 electrodes show lower charge-transfer resistance and higher lithium diffusion coefficients. In addition, LiMn1.4Ni0.55Mo0.05O4 cathode exhibits the smallest particle size, the lowest charge-transfer resistance and the highest lithium diffusion coefficient among all samples, indicating that it has a high reversibility and good rate capability.

  18. Stability Limits of the Liquid Phase in the Layered Mo/Pb/Mo, Mo/Bi/Mo and Mo/In/Mo Film Systems

    Directory of Open Access Journals (Sweden)

    S.I. Petrushenko

    2016-12-01

    Full Text Available The results of the study of supercooling of the fusible metals films between the continuous layers of molybdenum during the crystallization are given. Due to an original in situ technique based on the changes of resistance of samples during heating and cooling directly in the vacuum chamber the values of supercooling in Mo/Pb/Mo, Mo/Bi/Mo, Mo/In/Mo films are determined and the influence of the morphological structure of the bismuth inclusions on the temperature and nature of its supercooled melt crystallization has been found. The substrate temperature change during the condensation of samples, accompanied by a corresponding change in their microstructure, allows realizing both avalanche and diffuse crystallization and changing of supercooling value in the range of 60 to 180 K in Mo/Bi/Mo films.

  19. Bounds on the width, mass difference and other properties of X<mo stretchy='false'>(mo>>3872mn> stretchy='false'>)mo><mo>→mo>π<mo>+mo>π<mo>-mo>J<mo>/>ψ decays

    Energy Technology Data Exchange (ETDEWEB)

    Choi, S. -K.; Olsen, S. L.; Trabelsi, K.; Adachi, I.; Aihara, H.; Arinstein, K.; Asner, D. M.; Aushev, T.; Bakich, A. M.; Barberio, E.; Bay, A.; Belous, K.; Bhardwaj, V.; Bhuyan, B.; Bischofberger, M.; Bondar, A.; Bozek, A.; Bračko, M.; Brodzicka, J.; Brovchenko, O.; Browder, T. E.; Chang, P.; Chen, A.; Chen, P.; Cheon, B. G.; Chilikin, K.; Cho, I. -S.; Cho, K.; Choi, Y.; Dalseno, J.; Doležal, Z.; Drásal, Z.; Drutskoy, A.; Eidelman, S.; Epifanov, D.; Fast, J. E.; Gaur, V.; Gabyshev, N.; Garmash, A.; Goh, Y. M.; Golob, B.; Haba, J.; Hara, T.; Hayasaka, K.; Hayashii, H.; Horii, Y.; Hoshi, Y.; Hou, W. -S.; Hsiung, Y. B.; Hyun, H. J.; Iijima, T.; Inami, K.; Ishikawa, A.; Itoh, R.; Iwabuchi, M.; Iwasaki, Y.; Iwashita, T.; Joshi, N. J.; Julius, T.; Kang, J. H.; Katayama, N.; Kawasaki, T.; Kichimi, H.; Kim, H. J.; Kim, H. O.; Kim, J. B.; Kim, J. H.; Kim, K. T.; Kim, M. J.; Kim, S. K.; Kim, Y. J.; Kinoshita, K.; Ko, B. R.; Kobayashi, N.; Koblitz, S.; Kodyš, P.; Korpar, S.; Križan, P.; Kuhr, T.; Kumita, T.; Kuzmin, A.; Kwon, Y. -J.; Lange, J. S.; Lee, M. J.; Lee, S. -H.; Li, J.; Li, X.; Li, Y.; Libby, J.; Lim, C. -L.; Liu, C.; Liu, Y.; Liventsev, D.; Louvot, R.; Matvienko, D.; McOnie, S.; Miyabayashi, K.; Miyata, H.; Miyazaki, Y.; Mizuk, R.; Mohanty, G. B.; Mussa, R.; Nagasaka, Y.; Nakano, E.; Nakao, M.; Natkaniec, Z.; Neubauer, S.; Nishida, S.; Nishimura, K.; Nitoh, O.; Ogawa, S.; Ohshima, T.; Okuno, S.; Onuki, Y.; Pakhlov, P.; Pakhlova, G.; Park, H.; Park, H. K.; Park, K. S.; Pestotnik, R.; Petrič, M.; Piilonen, L. E.; Poluektov, A.; Röhrken, M.; Ryu, S.; Sahoo, H.; Sakai, K.; Sakai, Y.; Sanuki, T.; Schneider, O.; Schwanda, C.; Schwartz, A. J.; Senyo, K.; Seon, O.; Sevior, M. E.; Shapkin, M.; Shebalin, V.; Shibata, T. -A.; Shiu, J. -G.; Simon, F.; Singh, J. B.; Smerkol, P.; Sohn, Y. -S.; Sokolov, A.; Solovieva, E.; Stanič, S.; Starič, M.; Sumihama, M.; Sumiyoshi, T.; Tatishvili, G.; Teramoto, Y.; Uchida, M.; Uehara, S.; Uglov, T.; Unno, Y.; Uno, S.; Vahsen, S. E.; Varner, G.; Varvell, K. E.; Vinokurova, A.; Wang, C. H.; Wang, M. -Z.; Wang, P.; Wang, X. L.; Watanabe, M.; Watanabe, Y.; Williams, K. M.; Won, E.; Yabsley, B. D.; Yamashita, Y.; Yamauchi, M.; Yuan, C. Z.; Zhang, C. C.; Zhilich, V.; Zhulanov, V.; Zupanc, A.; Zyukova, O.

    2011-09-07

    We present results from a study of X(3872)→ππJ/ψ decays produced via exclusive B→KX(3872) decays. We determine the mass to be MX(3872)=(3871.85±0.27(stat)±0.19(syst)) MeV, a 90% confidence level upper limit on the natural width of ΓX(3872)<1.2 MeV, the product branching fraction B(B+→K+X(3872))×B(X(3872)→π+π-J/ψ)=(8.63±0.82(stat)±0.52(syst))×10-6, and a ratio of branching fractions B(B0→K0X(3872))/B(B+→K+X(3872))=0.50±0.14(stat)±0.04(syst). The difference in mass between the X(3872)→π+π-J/ψ signals in B+ and B0 decays is ΔMX(3872)=(-0.71±0.96(stat)±0.19(syst)) MeV. A search for a charged partner of the X(3872) in the decays B0→K-X+ or B+→K0X+, X+→π+π0J/ψ resulted in upper limits on the product branching fractions for these processes that are well below expectations for the case that the X(3872) is the neutral member of an isospin triplet. In addition, we examine possible JPC quantum number assignments for the X(3872) based on comparisons of angular correlations between final state particles in X(3872)→π+π-J/ψ decays with simulated data for JPC values of 1++ and 2-+. We examine the influence of ρ-ω interference in the M(π+π-) spectrum. The analysis is based on a 711 fb-1 data sample that contains 772×106 BB meson pairs collected at the Υ(4S) resonance in the Belle detector at the KEKB e+e- collider.

  20. Investigation of the site preference in Mn{sub 2}RuSn using KKR-CPA-LDA calculation

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Ling; Liu, Bohua [School of Material Science and Engineering, Hebei University of Technology, Tianjin 300130 (China); Luo, Hongzhi, E-mail: luo_hongzhi@163.com [School of Material Science and Engineering, Hebei University of Technology, Tianjin 300130 (China); Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100190 (China); Meng, Fanbin; Liu, Heyan [School of Material Science and Engineering, Hebei University of Technology, Tianjin 300130 (China); Liu, Enke; Wang, Wenhong; Wu, Guangheng [Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100190 (China)

    2015-05-15

    We investigated the site preference and atomic disorder between the A and C sites in Heusler alloy Mn{sub 2}RuSn by using the KKR-CPA-LDA method. It is found that, at ground state 0 K, the Hg{sub 2}CuTi-type (XA) structure is energetically favored, in which one Mn and one Ru occupy the A and C sites, respectively. The ground state energy of Mn{sub 2}RuSn increases with increasing degree of Mn (A)–Ru (C) atomic disorder. The equilibrium lattice constants also show a similar tendency. The Mn (A)–Ru (C) disorder lower the total spin moment effectively, which is 1.87 μ{sub B} in the XA structure and only 0.98 μ{sub B} in the L2{sub 1}B structure. In Mn{sub 2}RuSn with different degree of Mn (A)–Ru (C) atomic disorder, the total moments are always determined by the antiparallel aligned Mn (A, C) and Mn (B) spin moments. The saturated moment of Mn{sub 2}RuSn at 5 K is 1.68 μ{sub B}, which corresponds to ∼11% antisite Mn entering the C site. This Mn (A)–Ru (C) disorder in samples can be related to the contributions from entropy of mixing at elevated temperatures, especially when this sample is quenched from high temperatures. - Highlights: • Atomic disorder in Heusler alloy Mn{sub 2}RuSn has been investigated by the KKR-CPA method. • Hg{sub 2}CuTi-type structure is energetically favored in Mn{sub 2}RuSn. • Mn (A)–Ru (C) disorder obviously influence the magnetic properties of Mn{sub 2}RuSn.

  1. Synthesis of Novel Fluorescent Sensors Based on Naphthalimide Fluorophores for the Highly Selective Hg2+-Sensing

    Directory of Open Access Journals (Sweden)

    Yordkhuan Tachapermpon

    2015-01-01

    Full Text Available With an aim to develop the new sensors for optical detection of Hg2+ ions, two novel fluorometric sensors were designed and successfully prepared using 2-(3-(2-aminoethylsulfanylpropylsulfanylethanamine and one or two N-methylnaphthalimide moieties (1 and 2. Sensor 1 was obtained via N-alkylation, N-imidation and a one-pot nucleophilic aromatic substitution, and N-formylation of the amine, while sensor 2 was prepared via N-alkylation, N-imidation, and nucleophilic aromatic substitution. The characterization, including 1H NMR, 13C NMR, and mass spectrometry, was then performed for 1 and 2. The Hg2+-binding behaviors of the sensors were investigated in terms of sensitivity and selectivity by fluorescence spectroscopy. Sensor 1 especially provided the reversible and highly Hg2+-selective ON-OFF fluorescence behavior by discriminating various interfering ions such as Pb2+, Co2+, Cd2+, Mn2+, Fe2+, K+, Na+, and in particular Cu2+ and Ag+ with a detection limit of 22 ppb toward Hg2+ ions.

  2. MoEDAL expands

    CERN Multimedia

    Anaïs Schaeffer

    2011-01-01

    The MoEDAL collaboration deployed a test array of 18 plastic Nuclear Track Etch Detector (NTD) stacks – covering an area of 1 m2 – in the MoEDAL/VELO cavern at Point 8 of the LHC ring in November 2009. This small array was supplemented by a further 110 stacks this past January. The MoEDAL test array, which now covers an area of 8 m2, will reveal its secrets early in 2013. The full MoEDAL detector will be installed in the next long shutdown of the LHC in 2013.   View of the MoEDAL detectors installed at Point 8 of the LHC ring in January 2011. MoEDAL (Monopole and Exotics Detector At the LHC), the seventh LHC experiment, was approved by the CERN Research Board at the end of 2009. Its goal is to search for very specific exotics such as highly ionising massive stable (or pseudo-stable) particles with conventional electrical charge and magnetic monopoles. “The main LHC experiments are designed to detect conventionally charged particles, with conventional ionisation patte...

  3. Relationship Between Soil Properties and Different Fractions of Soil Hg

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Correlation and path analysis methods were used to study the relationship between soil properties and the distribution of different soil Hg fractions with nine representative soils from Chongqing, China. Results showed that clay (< 2 m) could increase water-soluble Hg (r = 0.700*). Soil organic matter (OM) could enhance the increase of elemental Hg (r = 0.674*). The higher the base saturation percentage (BSP), the more the residual Hg (r = 0.684*). Organic Hg, the sum of acid-soluble organic Hg. and alkali-soluble Hg, was positively affected by silt (2~20μm) but negatively affected by pH, with the direct path coefficients amounting to 1.0487 and 0.5121, respectively. The positive effect of OM and negative effect of BSP on organic Hg were the most significant, with the direct path coefficients being 0.7614 and -0.8527, respectively. The indirect effect of clay (< 2 μm) via BSP (path coefficient = 0.4186) was the highest, showing that the real influencing factor in the effect of clay (< 2 μm) on acid-soluble organic Hg was BSP. Since the available Hg fraction, water-soluble Hg, was positively affected by soil clay content, and the quite immobile and not bioavailable residual Hg by soil BSP, suitable reduction of clay content and increase of BSP would be of much help to reduce the Hg availability and Hg activity in Hg-contaminated soils.

  4. Vaporization thermodynamic studies by high-temperature mass spectrometry on some three-phase regions over the MnO-TeO2 binary line in the Mn-Te-O ternary system.

    Science.gov (United States)

    Narasimhan, T S Lakshmi; Sai Baba, M; Viswanathan, R

    2006-12-28

    Knudsen effusion mass spectrometric measurements have been performed in the temperature range of 850-950 K over four three-phase mixtures, each phase mixture having at least one phase lying on the MnO-TeO2 binary line of the Mn-Te-O phase diagram, and the rest of the phases lying above this binary line. The three-phase mixtures investigated are Mn3O4 + MnO + Mn6Te5O16; Mn3O4 + Mn6Te5O16 + MnTeO3; Mn3O4 + Mn3TeO6 + MnTeO3; and Mn3TeO6 + MnTeO3 + Mn2Te3O8. The vapor pressures of the gaseous species TeO2, TeO, and Te2 over these three-phase mixtures were measured, and various heterogeneous solid-gas reactions were evaluated along with the homogeneous gas-phase reaction TeO2(g) + 0.5Te2(g) = 2 TeO(g). The enthalpy and Gibbs free energy of formation of the four ternary Mn-Te-O phases were deduced at T = 900 K. These values (in kJ.mol-1), along with the estimated uncertainties in them are Delta(f)H(o)m = 4150 +/- 19, 752 +/- 11, 1710 +/- 11, 1924 +/- 40, and Delta(f)G(o)m= 2835 +/- 28, 511 +/- 11, 1254 +/- 19, 1238 +/- 38, for Mn6Te5O16, MnTeO3, Mn3TeO6, and Mn2Te3O8, respectively. A thermochemical assessment was made to examine the conditions under which the ternary Mn-Te-O phases could be formed on a stainless steel clad of mixed-oxide-fueled (MO2; M = U + Pu) fast breeder nuclear reactors. The phase Mn3TeO6 could be formed when the fuel is even slightly hyperstoichiometric (O/M = 2.0002) and the phase Mn6Te5O16 could also be formed when O/M = 2.0004. The threshold tellurium potential for the formation of Mn3TeO6 is higher than that for MnTe0.80 and CrTe1.10, but is comparable to that for MoTe1.10, and even lower than that for FeTe0.81 or NiTe0.63.

  5. A One-Dimensional Magnet Based on [Mo(III)(CN)7](4.).

    Science.gov (United States)

    Wei, Xiao-Qin; Qian, Kun; Wei, Hai-Yan; Wang, Xin-Yi

    2016-06-01

    Self-assembly of the [Mo(III)(CN)7](4-) anion and the Mn(II) unit with a macrocyclic ligand results in the first example of a one-dimensional (1D) chain compound based on the heptacyanomolybdate, [Mn(LN5C10)]2[Mo(CN)7]·2H2O (LN5C10 = 1,4,7,10,13-pentaazacyclopentadecane). Because of the existence of the interchain magnetic coupling, long-rang magnetic ordering was observed in this compound.

  6. Hg/HgO electrode and hydrogen evolution potentials in aqueous sodium hydroxide

    Energy Technology Data Exchange (ETDEWEB)

    Nickell, Ryan A.; Zhu, Wenhua H.; Payne, Robert U.; Cahela, Donald R.; Tatarchuk, Bruce J. [Center for Microfibrous Materials Manufacturing, Department of Chemical Engineering, 230 Ross Hall, Auburn University, Auburn, AL 36849 (United States)

    2006-10-27

    The Hg/HgO electrode is usually utilized as a reference electrode in alkaline solution such as for development of an alkaline hydrogen electrode. The reference electrode provides a suitable reference point but is available from few commercial vendors and suffers from inadequate documentation on potential in varying electrolytes. A new numerical method uses activity, activity coefficients, and a few correlated empirical equations to determine the potential values in both dilute and concentrated sodium hydroxide solutions at temperatures of 0-90{sup o}C and at concentrations of 0.100-12.8mol kg{sub H{sub 2}O}{sup -1}. The computed potentials of the Hg/HgO electrodes versus a normal hydrogen electrode (NHE) at 25{sup o}C and 1atm are 0.1634V for 0.100m, 0.1077V for 1.00m, and 0.0976V for 1.45m NaOH solutions. The Hg/HgO reduction potential further changes to -0.0751V versus NHE and hydrogen evolution potential changes to -0.9916V versus NHE in a solution of 30.0wt.% NaOH at 80{sup o}C. The calculated values are compared with the measured data at 25 and 75{sup o}C. The experimental data agree well with the numerical values computed from the theoretical and empirical equations. (author)

  7. Hg/HgO electrode and hydrogen evolution potentials in aqueous sodium hydroxide

    Science.gov (United States)

    Nickell, Ryan A.; Zhu, Wenhua H.; Payne, Robert U.; Cahela, Donald R.; Tatarchuk, Bruce J.

    The Hg/HgO electrode is usually utilized as a reference electrode in alkaline solution such as for development of an alkaline hydrogen electrode. The reference electrode provides a suitable reference point but is available from few commercial vendors and suffers from inadequate documentation on potential in varying electrolytes. A new numerical method uses activity, activity coefficients, and a few correlated empirical equations to determine the potential values in both dilute and concentrated sodium hydroxide solutions at temperatures of 0-90 °C and at concentrations of 0.100-12.8 mol k gH2O-1 . The computed potentials of the Hg/HgO electrodes versus a normal hydrogen electrode (NHE) at 25 °C and 1 atm are 0.1634 V for 0.100m, 0.1077 V for 1.00m, and 0.0976 V for 1.45m NaOH solutions. The Hg/HgO reduction potential further changes to -0.0751 V versus NHE and hydrogen evolution potential changes to -0.9916 V versus NHE in a solution of 30.0 wt.% NaOH at 80 °C. The calculated values are compared with the measured data at 25 and 75 °C. The experimental data agree well with the numerical values computed from the theoretical and empirical equations.

  8. Long-term Hg pollution induced Hg tolerance in the terrestrial isopod Porcellio scaber (Isopoda, Crustacea)

    Energy Technology Data Exchange (ETDEWEB)

    Lapanje, A. [University of Ljubljana, Biotechnical Faculty, Department of Biology, Vecna pot 111, 1000 Ljubljana (Slovenia); Institute of Physical Biology, Veliko Mlacevo 59, 1290 Grosuplje (Slovenia)], E-mail: ales.lapanje@bf.uni-lj.si; Drobne, D. [University of Ljubljana, Biotechnical Faculty, Department of Biology, Vecna pot 111, 1000 Ljubljana (Slovenia); Nolde, N. [Institute Jozef Stefan, Department of Environmental Sciences, Jamova 39, 1000 Ljubljana (Slovenia); Valant, J. [University of Ljubljana, Biotechnical Faculty, Department of Biology, Vecna pot 111, 1000 Ljubljana (Slovenia); Muscet, B. [Institute of Physical Biology, Veliko Mlacevo 59, 1290 Grosuplje (Slovenia); Leser, V. [University of Ljubljana, Biotechnical Faculty, Department of Biology, Vecna pot 111, 1000 Ljubljana (Slovenia); Rupnik, M. [Institute of Public Health, Prvomajska 1, 2000 Maribor (Slovenia); Faculty of Medicine, University of Maribor, Slomskov trg 15, 2000 Maribor (Slovenia)

    2008-06-15

    The aim of our work was to assess the pollution-induced community tolerance (PICT) of isopod gut microbiota and pollution-induced isopod population tolerance (PIPT). Animals collected from a chronically Hg polluted and an unpolluted location were exposed for 14 days to 10 {mu}g Hg/g dry food under laboratory conditions. The lysosomal membrane stability, hepatopancreas epithelium thickness, feeding activity and animal bacterial gut microbiota composition were determined. The results confirm the hypothesis that the response to short-term Hg exposure differs for animals from the Hg polluted and the unpolluted field locations. The animals and their gut microbiota from the Hg polluted location were less affected by Hg in a short-term feeding experiment than those from the unpolluted environment. We discuss the pollution-induced population tolerance of isopods and their gut microbiota as a measure of effects of long-term environmental pollution. The ecological consequences of such phenomena are also discussed. - Isopods (Porcellio scaber) as well as their bacterial gut community from a mercury-polluted site are mercury tolerant.

  9. Microstructure and Mechanical Properties of Mn-Containing Maraging Steels

    Science.gov (United States)

    Hamed Zargari, Habib; Hossein Nedjad, Syamak

    2015-09-01

    An attempt to the modification of the microstructure and mechanical properties of affordable, Mn-containing maraging alloys is reported. These alloys have demonstrated strong age hardening but suffered with premature intergranular brittleness despite their potential applications in tooling, dies, and machinery industries. An Fe-10Ni-6Mo-3Mn-1Ti (wt.%) alloy was prepared by vacuum melting and processed by homogenization (1250 °C/48 h), cold rolling, solution annealing (950 °C/1 h), and aging treatments (500 °C/4 h). It presented tensile strength of about 2.65 GPa, a few percent of tensile elongation and a mixed ductile-brittle fracture mode. Transmission electron microscopy (TEM) revealed the precipitation of a nearly spherical phase. Crystal symmetry of the second phase precipitates was identified hexagonal close-packed corresponding reasonably to the Fe2Mo Laves phase having lattice parameters of a = 0.4745 and c = 0.7754 nm. Precipitation of a Mo-enriched second-phase particle was occasionally found at prior austenite grain boundaries but the pronounced grain boundary precipitation was never identified. Energy-filtering transmission electron microscopy using the Mo-M4,5 post edge revealed remarkable segregation of Mo at grain boundaries.

  10. MBE HgCdTe heterostructure detectors

    Science.gov (United States)

    Schulman, Joel N.; Wu, Owen K.

    1990-01-01

    HgCdTe has been the mainstay for medium (3 to 5 micron) and long (10 to 14 micron) wavelength infrared detectors in recent years. Conventional growth and processing techniques are continuing to improve the material. However, the additional ability to tailor composition and placement of doped layers on the tens of angstroms scale using molecular beam epitaxy (MBE) provides the opportunity for new device physics and concepts to be utilized. MBE-based device structures to be discussed here can be grouped into two categories: tailored conventional structures and quantum structures. The tailored conventional structures are improvements on familiar devices, but make use of the ability to create layers of varying composition, and thus band gap, at will. The heterostructure junction can be positioned independently of doping p-n junctions. This allows the small band gap region in which the absorption occurs to be separated from a larger band gap region in which the electric field is large and where unwanted tunneling can occur. Data from hybrid MBE/liquid phase epitaxy (LPE)/bulk structures are given. Quantum structures include the HgTe-CdTe superlattice, in which the band gap and transport can be controlled by alternating thin layers (tens of angstroms thick) of HgTe and CdTe. The superlattice has been shown to exhibit behavior which is non-alloy like, including very high hole mobilities, two-dimensional structure in the absorption coefficient, resonant tunneling, and anisotropic transport.

  11. Magnetic transition anisotropies in orthorhombic LuMnO3 and HoMnO3 multiferroic thin films

    Science.gov (United States)

    Tsai, T. Y.; Lin, T. H.; Slowry, S.; Luo, C. W.; Wu, K. H.; Lin, J.-Y.; Uen, T. M.; Juang, J. Y.

    2010-01-01

    We have successfully prepared the b-axis-oriented orthorhombic LuMnO3 (LuMO) and HoMnO3 (HMO) thin films by pulsed laser deposition on (110)-LaAlO3 substrates. The nearly perfect alignment between the film growth orientation and the substrate allows us to study the magnetic transitions along the respective crystal orientation, which has displayed marked anisotropic behaviours. In particular, with the largest ionic size difference between Lu and Ho for the family of RMnO3 displaying the E-type AFM, the effects of lattice distortion on the magnetic transition are compared.

  12. Long-distance transport of Hg, Sb, and As from a mined area, conversion of Hg to methyl-Hg, and uptake of Hg by fish on the Tiber River basin, west-central Italy

    Science.gov (United States)

    Gray, John E.; Rimondi, Valentina; Costagliola, Pilario; Vaselli, Orlando; Lattanzi, Pierfranco

    2014-01-01

    Stream sediment, stream water, and fish were collected from a broad region to evaluate downstream transport and dispersion of mercury (Hg) from inactive mines in the Monte Amiata Hg District (MAMD), Tuscany, Italy. Stream sediment samples ranged in Hg concentration from 20 to 1,900 ng/g, and only 5 of the 17 collected samples exceeded the probable effect concentration for Hg of 1,060 ng/g, above which harmful effects are likely to be observed in sediment-dwelling organisms. Concentrations of methyl-Hg in Tiber River sediment varied from 0.12 to 0.52 ng/g, and although there is no established guideline for sediment methyl-Hg, these concentrations exceeded methyl-Hg in a regional baseline site (Sb (Sb) and for protection against chronic effects to aquatic wildlife (150 μg/L for As and 5.6 μg/L for Sb). Concentrations of Hg in freshwater fish muscle ranged from 0.052–0.56 μg/g (wet weight), mean of 0.17 μg/g, but only 17 % (9 of 54) exceeded the 0.30 μg/g (wet weight) USEPA fish muscle guideline recommended to protect human health. Concentrations of Hg in freshwater fish in this region generally decreased with increasing distance from the MAMD, where fish with the highest Hg concentrations were collected more proximal to the MAMD, whereas all fish collected most distal from Hg mines contained Hg below the 0.30 μg/g fish muscle guideline. Data in this study indicate some conversion of inorganic Hg to methyl-Hg and uptake of Hg in fish on the Paglia River, but less methylation of Hg and Hg uptake by freshwater fish in the larger Tiber River.

  13. Hg Vetical Transference in Soil—Water System

    Institute of Scientific and Technical Information of China (English)

    GUOYIJUN; MOUSUSEN; 等

    1998-01-01

    Hg vertial transference in soil-water system was studied by analyzing Hg vertical ditribution in soil column after adding Hg and one of the two leacheates,deionzied water or acid rain,into soil column.The results indicated that Hg was hardly transferable in puple soil.About 86%-88% of the total soil Hg was distributed in the top layer (0-2cm) and to Hg was detected in the leakage when the purple soil column was leached by deionized water and simulated acid rain.But Hg was more movalbe in yellow soil with only about 20%-22% of the total soil Hg distributed in the top layer (0-2cm),and about 17%-25% washed out from the soil column by deionized water and simulted acid rain,Incremant in soil bulk density colud reduce Hg leaching,thus the more the Hg kept in soil,the less the Hg leached into underground water,Deionized water and acid rain almost played the same role in leaching Hg.Bentioint was most effecient in preventing Hg from vertcal transferring in the soil coulumn.

  14. RoMo

    DEFF Research Database (Denmark)

    Pedersen, Esben Warming; Hornbæk, Kasper

    2011-01-01

    In TUIs, physical/digital conflicts can occur when the digital model does not match the model implied by the spatial lay- out of tangibles. We show how tangible tabletop interfaces (TTI) can be modified to allow robot movement of tangi- bles, thereby avoiding conflicts. We present RoMo, an open...

  15. Process of [sup 196]Hg enrichment

    Science.gov (United States)

    Grossman, M.W.; Mellor, C.E.

    1993-04-27

    A simple rate equation model shows that by increasing the length of the photochemical reactor and/or by increasing the photon intensity in said reactor, the feedstock utilization of [sup 196]Hg will be increased. Two preferred embodiments of the present invention are described, namely (1) long reactors using long photochemical lamps and vapor filters; and (2) quartz reactors with external UV reflecting films. These embodiments have each been constructed and operated, demonstrating the enhanced utilization process dictated by the mathematical model (also provided).

  16. Process of .sup.196 Hg enrichment

    Science.gov (United States)

    Grossman, Mark W.; Mellor, Charles E.

    1993-01-01

    A simple rate equation model shows that by increasing the length of the photochemical reactor and/or by increasing the photon intensity in said reactor, the feedstock utilization of .sup.196 Hg will be increased. Two preferred embodiments of the present invention are described, namely (1) long reactors using long photochemical lamps and vapor filters; and (2) quartz reactors with external UV reflecting films. These embodiments have each been constructed and operated, demonstrating the enhanced utilization process dictated by the mathematical model (also provided).

  17. Removal of Hg (II and Mn (II from aqueous solution using nanoporous carbon impregnated with surfactants

    Directory of Open Access Journals (Sweden)

    Mansoor Anbia

    2016-09-01

    Full Text Available Mesoporous carbons were impregnated with the anionic and cationic surfactants to increase adsorbing capacity for heavy metal ions. Prepared samples were characterized by X-ray diffraction (XRD and nitrogen adsorption–desorption isotherms. Batch adsorption studies were carried out to study the effect of various parameters like contact time, pH, metal ion concentration and agitation speed. The mercury removal by cationic surfactant cetyltrimethyl ammonium bromide (CTAB, anionic surfactant sodium dodecyl sulfate (SDS modified mesoporous carbon and unmodified mesoporous carbon were found to be 94%, 81.6% and 54.5%, respectively while the manganese removal for these adsorbents were found to be 82.2%, 70.5% and 56.8%, respectively. The sorption data were fit better with the Langmuir adsorption isotherm than Freundlich isotherm.

  18. The presence of Nd and Pr in HgMn stars

    OpenAIRE

    Dolk, Linus; Wahlgren, Glenn; Lundberg, Hans; Li, Zhongshan; Litzén, Ulf; Ivarsson, Stefan; Ilyin, I.; S. Hubrig

    2002-01-01

    Optical region spectra for a number of upper main sequence chemically peculiar (CP) stars have been observed to study singly and doubly ionized praseodymium and neodymium lines. In order to improve existing atomic data of these elements, laboratory measurements have been carried out with the Lund VUV Fourier Transform Spectrometer (FTS). From these measurements wavelengths and hyperfine structure (hfs) have been studied for selected , and lines of astrophysical interest. Radiative life times ...

  19. The presence of Nd and Pr in HgMn stars

    OpenAIRE

    Dolk, Linus; Wahlgren, Glenn; Lundberg, Hans; Li, Zhongshan; Litzén, Ulf; Ivarsson, Stefan; Ilyin, I.; S. Hubrig

    2002-01-01

    Optical region spectra for a number of upper main sequence chemically peculiar (CP) stars have been observed to study singly and doubly ionized praseodymium and neodymium lines. In order to improve existing atomic data of these elements, laboratory measurements have been carried out with the Lund VUV Fourier Transform Spectrometer (FTS). From these measurements wavelengths and hyperfine structure (hfs) have been studied for selected , and lines of astrophysical interest. Radiative life time...

  20. Phase instability of thermally aged CrMn austenitic steels

    Science.gov (United States)

    Ruedl, E.; Sasaki, T.

    1984-05-01

    The microstructural changes taking place in several commercial Cr-Mn austenitic steels during ageing at 873 and 1073 K were examined by analytical electron microscopy. Phase identification was obtained by electron diffraction, energy dispersive X-ray analysis and electron energy loss spectrometry. It was found that the phase changes depend on the carbon and nitrogen content of the materials as well as on the presence of Mo and delta ferrite.

  1. Hall effect of quinquevalent ion-doped La0.9Sb0.1MnO3 film

    Institute of Scientific and Technical Information of China (English)

    WANG Dengjing; WANG Mei; WANG Ruwu; LI Yunbao

    2013-01-01

    Hall effect of the quinquevalent ion-doped La0.gSb0.1MnO3 (LSbMO) film,with strong magnetic-resistive correlation,which was believed to be an electron-doped manganite,was experimentally studied,and a positive normal Hall coefficient was observed below the Curie temperature,which indicated that the system was hole doped.These observations might be attributed to the presence of excessive oxygen in the film.The resistivity of the film increased overall and the metal-semiconductor transition shifted to a lower temperature after removing excessive oxygen by vacuum annealing.These results implied that the magnetic-resistive correlation in the LSbMO film was attributed to the interaction between Mn3+ and Mn4+ ions,instead of that between Mn2+ and Mn3+ ions.

  2. Investigation of the site preference in Mn2RuSn using KKR-CPA-LDA calculation

    Science.gov (United States)

    Yang, Ling; Liu, Bohua; Luo, Hongzhi; Meng, Fanbin; Liu, Heyan; Liu, Enke; Wang, Wenhong; Wu, Guangheng

    2015-05-01

    We investigated the site preference and atomic disorder between the A and C sites in Heusler alloy Mn2RuSn by using the KKR-CPA-LDA method. It is found that, at ground state 0 K, the Hg2CuTi-type (XA) structure is energetically favored, in which one Mn and one Ru occupy the A and C sites, respectively. The ground state energy of Mn2RuSn increases with increasing degree of Mn (A)-Ru (C) atomic disorder. The equilibrium lattice constants also show a similar tendency. The Mn (A)-Ru (C) disorder lower the total spin moment effectively, which is 1.87 μB in the XA structure and only 0.98 μB in the L21B structure. In Mn2RuSn with different degree of Mn (A)-Ru (C) atomic disorder, the total moments are always determined by the antiparallel aligned Mn (A, C) and Mn (B) spin moments. The saturated moment of Mn2RuSn at 5 K is 1.68 μB, which corresponds to ∼11% antisite Mn entering the C site. This Mn (A)-Ru (C) disorder in samples can be related to the contributions from entropy of mixing at elevated temperatures, especially when this sample is quenched from high temperatures.

  3. Gold nanoparticles generated through "green route" bind Hg2+ with a concomitant blue shift in plasmon absorption peak.

    Science.gov (United States)

    Radhakumary, C; Sreenivasan, K

    2011-07-21

    We discuss here a quick, simple, economic and ecofriendly method through a completely green route for the selective detection of Hg(2+) in aqueous samples. Here we exploited the ability of chitosan to generate gold nanoparticles and subsequently to act as a stabilizer for the formed nanoparticles. When chitosan stabilized gold nanoparticles (CH-Au NPs) are interacted with Hg(2+) a blue shift for its localized surface plasmon resonance absorbance (LSPR) band is observed. The blue shift is reasoned to be due to the formation of a thin layer of mercury over gold. A concentration as low as 0.01 ppm to a maximum of 100 ppm Hg(2+) can be detected based on this blue shift of the CH-Au NPs. While all other reported methods demand complex reaction steps and costly chemicals, the method we reported here is a simple, rapid and selective approach for the detection of Hg(2+). Our results also show that the CH-Au NPs have excellent selectivity to Hg(2+) over common cations namely, Pb(2+), Cd(2+), Mn(2+), Fe(2+), Ag(1+), Ce(4+), Ni(2+), and Cu(2+).

  4. HgZnTe-based detectors for LWIR NASA applications

    Science.gov (United States)

    Patten, Elizabeth A.; Kalisher, Murray H.

    1990-01-01

    The initial goal was to grow and characterize HgZnTe and determine if it indeed had the advantageous properties that were predicted. Researchers grew both bulk and liquid phase epitaxial HgZnTe. It was determined that HgZnTe had the following properties: (1) microhardness at least 50 percent greater than HgCdTe of equivalent bandgap; (2) Hg annealing rates of at least 2 to 4 times longer than HgCdTe; and (3) higher Hg vacancy formation energies. This early work did not focus on one specific composition (x-value) of HgZnTe since NASA was interested in HgZnTe's potential for a variety of applications. Since the beginning of 1989, researchers have been concentrating, however, on the liquid phase growth of very long wavelength infrared (VLWIR) HgZnTe (cutoff approx. equals 17 microns at 65K) to address the requirements of the Earth Observing System (EOS). Since there are no device models to predict the advantages in reliability one can gain with increased microhardness, surface stability, etc., one must fabricate HgZnTe detectors and assess their relative bake stability (accelerated life test behavior) compared with HgCdTe devices fabricated in the same manner. Researchers chose to fabricate HIT detectors as a development vehicle for this program because high performance in the VLWIR has been demonstrated with HgCdTe HIT detectors and the HgCdTe HIT process should be applicable to HgZnTe. HIT detectors have a significant advantage for satellite applications since these devices dissipate much less power than conventional photoconductors to achieve the same responsivity.

  5. Fully relativistic coupled cluster and DFT study of electric field gradients at Hg in 199Hg compounds

    DEFF Research Database (Denmark)

    Arcisauskaité, Vaida; Knecht, Stefan; Sauer, Stephan P. A.

    2012-01-01

    We investigate the magnitude and interplay of relativistic and electron correlation effects on the electric field gradient (EFG) at the position of Hg in linear and bent HgL2 (L=CH3, Cl, Br, I) and trigonal planar [HgCl3]- complexes using four-component relativistic Dirac-Coulomb (DC) and non...

  6. Nuclear Structure Studies from Hg and Au Alpha Decay Chains

    Science.gov (United States)

    Goon, J. Tm.; Bingham, C. R.; Hartley, D. J.; Zhang, Jing-Ye; Riedinger, L. L.; Danchev, M.; Kondev, F. G.; Carpenter, M. P.; Janssens, R. V. F.; Abu Saleem, K. H.; Ahmad, I.; Davids, C. N.; Heinz, A.; Khoo, T. L.; Lauritsen, T.; Lister, C. J.; Poli, G. L.; Seweryniak, D.; Wiedenhover, I.; Ma, W. C.; Amro, H.; Reviol, W.; Cizewski, J. A.; Smith, M.

    2003-04-01

    Neutron deficient nuclei near the Z = 82 shell gap have been a source of great interest. This region is known to exhibit the phenomena of shape-coexistence and triaxiality. Alpha decay study of these nuclei coupled with gamma-rayspectroscopy data can give a better understanding of their nuclear structure properties. The decay chains of ^173-177Au and ^175-179Hg were studied following the bombardment of ^92,94,96Mo targets with ^84Sr beam from the ATLAS accelerator at the Argonne National Laboratory. The experiment utilized the Gammasphere array in conjunction with the Fragment Mass Analyzer (FMA) for mass identification and a Double-sided Silicon Strip Detector (DSSD) that was used to detect the recoiling implants and the alpha particles associated with each nuclide. An array of four Ge detectors and a low-energy photon spectrometer (LEPS) was used at the focal plane of the FMA to detect γ rays in coincidence with the α particles. This information was used to elucidate the α-decay fine structures. Inverse radioactive decay tagging was also useful in assigning certain fine structure α peaks to a particular nuclide. New α decay lines were observed and their energies, and half-lives were measured. These include fine structure lines in the α decays of ^174,176Au and ^173Pt. The decay schemes resulting from the fine structure observations will be presented. The α decay reduced widths are used to suggest spin and parity assignments. The structure of these states will be discussed in the framework of the Nilsson model and alpha decay selection rules. * This work is supported by the Department of Energy through contract numbers DE-FG02-96ER40983 (UT), W-31-109-ENG-38 (ANL), DE-FG02-95ER40939 (MSU), DE-FG05-88ER40406 (WU), and by the National Science Foundation (RU

  7. High Mn austenitic stainless steel

    Science.gov (United States)

    Yamamoto, Yukinori [Oak Ridge, TN; Santella, Michael L [Knoxville, TN; Brady, Michael P [Oak Ridge, TN; Maziasz, Philip J [Oak Ridge, TN; Liu, Chain-tsuan [Knoxville, TN

    2010-07-13

    An austenitic stainless steel alloy includes, in weight percent: >4 to 15 Mn; 8 to 15 Ni; 14 to 16 Cr; 2.4 to 3 Al; 0.4 to 1 total of at least one of Nb and Ta; 0.05 to 0.2 C; 0.01 to 0.02 B; no more than 0.3 of combined Ti+V; up to 3 Mo; up to 3 Co; up to 1W; up to 3 Cu; up to 1 Si; up to 0.05 P; up to 1 total of at least one of Y, La, Ce, Hf, and Zr; less than 0.05 N; and base Fe, wherein the weight percent Fe is greater than the weight percent Ni, and wherein the alloy forms an external continuous scale including alumina, nanometer scale sized particles distributed throughout the microstructure, the particles including at least one of NbC and TaC, and a stable essentially single phase FCC austenitic matrix microstructure that is essentially delta-ferrite-free and essentially BCC-phase-free.

  8. Radical polymerization of styrene controlled by half-sandwich Mo(III)/Mo(IV) couples: all basic mechanisms are possible.

    Science.gov (United States)

    Le Grognec, E; Claverie, J; Poli, R

    2001-10-03

    Density functional calculations of bond dissociation energies (BDEs) have been used as a guide to the choice of metal system suitable for controlling styrene polymerization by either the stable free radical polymerization (SFRP) or the atom transfer radical polymerization (ATRP) mechanism. In accord with the theoretical prediction, CpMo(eta(4)-C(4)H(6))(CH(2)SiMe(3))(2), 2, is not capable of yielding SFRP of styrene. Still in accord with theoretical prediction, CpMo(eta(4)-C(4)H(6))Cl(2), 1, CpMo(PMe(3))(2)Cl(2), 3, and CpMo(dppe)Cl(2) (dppe = 1,2-bis(diphenylphosphino)ethane), 4, yield controlled styrene polymerization by the SFRP mechanism in the presence of 2,2'-azobisisobutyronitrile (AIBN). This arises from the generation of a putative Mo(IV) alkyl species from the AIBN-generated radical addition to the Mo(III) compound. The controlled nature of the polymerizations is indicated by linear M(n) progression with the conversion in all cases and moderate polydispersity indices (PDIs). Controlled polymerization of styrene is also given by compounds 3 and 4 in combination with alkyl bromides. These complexes then operate by the ATRP mechanism, again in accord with the theoretical predictions. Controlled character is revealed by linear increase of M(n) versus conversion, low PDIs, a stop-and-go experiment, and (1)H NMR and MALDI-TOF analyses of the polymer end groups. The same controlled polymerization is given by a "reverse" ATRP experiment, starting from AIBN and CpMo(PMe(3))(2)Cl(2)Br, 5. On the other hand, when compound 1 or 2 is used in combination with an alkyl bromide (as for an ATRP experiment), the isolated polystyrene shows by M(n), (1)H NMR, and MALDI-TOF analyses that catalytic chain transfer (CCT) radical polymerization takes place in this case. Kinetics simulations underscore the conditions regulating the radical polymerization mechanism and the living character of the polymerization. The complexes herein described are ineffective at controlling the

  9. First-principles study on the ferrimagnetic half-metallic Mn2FeAs alloy

    Science.gov (United States)

    Qi, Santao; Zhang, Chuan-Hui; Chen, Bao; Shen, Jiang; Chen, Nanxian

    2015-05-01

    Mn-based full-Heusler alloys are kinds of promising candidates for new half-metallic materials. Basing on first principles, the electronic structures and magnetic properties of the Mn2FeAs full-Heusler alloy have been investigated in detail. The Hg2CuTi-type Mn2FeAs compound obeys the Slater-Pauling rule, while the anti-parallel alignment atomic magnetic moments of Mn locating at different sites indicate it a ferrimagnetic alloy. The calculated spin-down bands behave half-metallic character, exhibiting a direct gap of 0.46 eV with a 100% spin polarization at the Fermi level. More studies show the compound would maintain half-metallic nature in a large range of variational lattice constants. We expect that our calculated results may trigger Mn2FeAs applying in the future spintronics field.

  10. Bioindication of volcanic mercury (Hg) deposition around Mt Etna (Sicily)

    Science.gov (United States)

    Martin, R.; Witt, M. L.; Sawyer, G. M.; Watt, S.; Bagnato, E.; Calabrese, S.; Aiuppa, A.; Delmelle, P.; Pyle, D. M.; Mather, T. A.

    2012-12-01

    Mt. Etna is a major natural source of Hg to the Mediterranean region. Total mercury concentrations, [Hg]tot, in Castanea sativa (sweet chestnut) leaves sampled 7-13 km from Etna's vents (during six campaigns in 2005-2011) were determined using atomic absorption spectroscopy. [Hg]tot in C. sativa was greatest on Etna's SE flank reflecting Hg deposition from the typically overhead volcanic plume. When adjusted for leaf age, [Hg]tot in C. sativa also increased with recent eruptive activity. [Hg]tot in C. sativa was not controlled by [Hg]tot in soils, which instead was greatest on the (upwind) NW flank and correlated strongly with soil organic matter (% Org). Our results suggest that at least ~1% of Hg emitted from Etna is deposited proximally, supporting recent measurement and model results which indicate that GEM (Hg0; the dominant form of Hg in high temperature magmatic gases) is oxidised rapidly to RGM and Hgp in ambient temperature volcanic plumes. Samples of C. sativa and soils were also collected in July and September 2012 alongside SO2 and acid gas diffusion tube samples. These new samples will enable us to investigate Hg accumulation over a single growth season with reference to the exposure of vegetation to volcanic gases and particles.

  11. 汞在MnOx-CeO2/γ-Al2O3催化剂表面的赋存形态分析%Speciation of mercury formed on MnOx-CeO2/γ-Al2O3 catalyst surface

    Institute of Scientific and Technical Information of China (English)

    罗小雨; 苏胜; 向军; 汪一; 王鹏鹰; 尤默; 陆骑

    2015-01-01

    为了高效经济地控制燃煤电站汞的排放,探索新型SCR催化剂上汞的催化氧化具有重要的学术价值和广阔的应用前景。Hg0在 MnOx-CeO2/γ-Al2O3(MnCe15)催化剂上被氧化后会以多种形态存在于催化剂表面,为确定MnCe15催化剂上汞的化合物的赋存形态,使用程序升温热分解方法研究了纯汞化合物的分解曲线,并与在不同烟气条件下处理过的MnCe15催化剂的分解脱附曲线进行了对比。研究确认了反应中HgO、HgCl2、Hg(NO3)2和HgSO4的生成,并根据实验结果分析了相应的汞化合物生成的反应路径。结果表明,在模拟烟气条件下HgCl2是主要的异相催化反应产物,同时可以在催化剂表面检测到少量HgO和HgSO4的生成。这一结论可为研究SCR催化剂上Hg0的催化氧化机理提供基础。%Hg0 oxidation over selective catalytic reduction (SCR) catalysts would be of great scientific and practical value to control mercury emission in coal-fired power stations. To elucidate the mercury species existing on the MnOx-CeO2/γ-Al2O3(MnCe15) catalyst surface, a temperature programmed thermal decomposition (TPTD) method was used in this study to analyze the characteristics of the mercury species formed on the MnCe15 catalysts. A series of pure mercury compounds mixed with fresh MnCe15 were first studied for qualitative calibration. Then, the TPTD method was used to identify the Hg species on used MnCe15 catalysts pretreated under different operation conditions. The formation of HgO, HgCl2, Hg(NO3)2 and HgSO4 during the oxidation process was confirmed and the reaction pathways were proposed. The mercury species present were mainly HgCl2 after MnCe15 catalysts were used to oxidize Hg0 under simulated flue gas conditions. HgO and HgSO4 were found to exist in very low concentrations. This study provided the basis for the study on catalytic oxidation mechanism of Hg0 on SCR catalyst.

  12. Reconstruction of early Cambrian ocean chemistry from Mo isotopes

    Science.gov (United States)

    Wen, Hanjie; Fan, Haifeng; Zhang, Yuxu; Cloquet, Christophe; Carignan, Jean

    2015-09-01

    The Neoproterozoic-Cambrian transition was a key time interval in the history of the Earth, especially for variations in oceanic and atmospheric chemical composition. However, two conflicting views exist concerning the nature of ocean chemistry across the Precambrian-Cambrian boundary. Abundant geochemical evidence suggests that oceanic basins were fully oxygenated by the late Ediacaran, while other studies provide seemingly conflicting evidence for anoxic deep waters, with ferruginous conditions [Fe(II)-enriched] persisting into the Cambrian. Here, two early Cambrian sedimentary platform and shelf-slope sections in South China were investigated to trace early Cambrian ocean chemistry from Mo isotopes. The results reveal that early Cambrian sediments deposited under oxic to anoxic/euxinic conditions have δ98/95Mo values ranging from -0.28‰ to 2.29‰, which suggests that early Cambrian seawater may have had δ98/95Mo values of at least 2.29‰, similar to modern oceans. The heaviest and relatively homogeneous δ98/95Mo values were recorded in siltstone samples formed under completely oxic conditions, which is considered that Mn oxide-free shuttling was responsible for such heavy δ98/95Mo value. Further, combined with Fe species data and the accumulation extent of Mo and U, the variation of δ98/95Mo values in the two studied sections demonstrate a redox-stratified ocean with completely oxic shallow water and predominantly anoxic (even euxinic) deeper water having developed early on, which eventually became completely oxygenated. This suggests that oceanic circulation at the time became reorganized, and such changes in oceanic chemistry may have been responsible for triggering the "Cambrian Explosion" of biological diversity.

  13. Mass Independent Fractionation of Hg Isotopes Preserved in the Precambrian

    Science.gov (United States)

    Thibodeau, A. M.; Bergquist, B. A.; Kah, L. C.; Ono, S.; Ghosh, S.; Hazen, R. M.

    2013-12-01

    Mercury (Hg) is a photochemically active, redox-sensitive, chalcophilic metal with complex biogeochemistry that displays a wide range of mass-dependent (MDF) and mass-independent (MIF) stable isotopic fractionation. In the past decade, Hg isotopes have emerged as important tracers of both the sources and cycling of Hg in the modern environment. However, their utility as environmental proxies in ancient rocks remains largely unexplored. The potential of Hg isotopes to inform Precambrian environments derives from the observation that Hg isotopes with odd atomic mass numbers (199Hg and 201Hg) undergo large MIF by the magnetic isotope effect (MIE) and smaller MIF through the nuclear volume effect (NVE). Small MIF produced via NVE has been observed for numerous transformations and is characterized by MIF ratios (Δ199Hg/Δ201Hg) of about 1.6. Large Hg-MIF driven by MIE has been observed during photochemical transformations and is characterized by Δ199Hg/Δ201Hg ratios between 1 and 1.3. This MIF signal is sensitive to a range of environmental conditions, including the amount and type of solar radiation, the presence and type of complexing organic ligands, and the Hg/dissolved organic carbon (DOC) ratio. Thus, it is hoped that Hg-MIF signals may indirectly record changes in atmospheric composition or seawater chemistry if preserved in marine sedimentary records. Previous work has clearly demonstrated that Hg-MIF signals are preserved in Archean and Paleoproterozoic marine shales and massive sulfide deposits. Here, we present evidence that such signals are also preserved in marine shales of mid-Proterozoic age, including the ~1.3 Ga Sulky formation (Dismal Lakes Group, NW Arctic), the ~1.45 Ga Greyson Shale (Belt Basin, Montana), and the ~1.5 Ga Katalsy formation (Kypry Group, Eastern European Platform). We observe that the Greyson shale and shales within the Sulky formation yield negative Hg-MIF with Δ199Hg/Δ201Hg ratios close to 1 and that Kaltasy group sediments

  14. Superdeformation studies in {sup 191}Hg

    Energy Technology Data Exchange (ETDEWEB)

    Carpenter, M.P.; Janssens, R.V.F.; Crowell, B. [and others

    1995-08-01

    Superdeformation in the A {approximately} 190 region was first observed in {sup 191}Hg from an experiment performed at ATLAS using the Argonne Notre Dame {gamma}-ray facility. We recently revisited the study of superdeformation in this nucleus using Gammasphere and the {sup 160}Gd({sup 36}S,5n) and {sup 174}Yb({sup 22}Ne,5n) reactions at 172 and 120 MeV in order to populate and measure states in the second well. The goal of the experiment was to identify new bands in the data, and thus allow us to gain understanding on the relative placement of single particle orbitals near the N = 112 SD shell gap. From an analysis of the data, the three previously identified SD bands were extended, and their feeding into the yrast states delineated. Two new SD bands were observed and preliminary evidence for a third new band was obtained as well.

  15. The effect of Mn substitution on the structure and magnetic properties of Se(Cu sub 1 sub - sub x Mn sub x)O sub 3 solid solution

    CERN Document Server

    Escamilla, R; Rosales, M I; Moran, E C; Alario-Franco, M A

    2003-01-01

    The effects of Mn substitution on the structure and magnetic properties of the SeMO sub 3 (M = Cu sub 1 sub - sub x Mn sub x) solid solution have been studied. Rietveld refinements of the x-ray diffraction patterns of these samples indicate that the manganese ions occupy copper sites. This replacement induces significant changes in the M-O bond lengths that give rise to abrupt decreases of the [M-O sub 6] octahedral distortion. In contrast, the M-O(1)-M and M-O(2)-M bond angles remain essentially constant. The magnetic behaviour of this solid solution was studied in the temperature range of 2 K < T < 300 K. The temperature dependence of the inverse magnetic susceptibility is well described by the Curie-Weiss law at high temperatures, in the composition range studied. We found that the substitution of Mn for Cu induces a sharp drop in the saturation moment of SeCuO sub 3. At about 10% of Mn there is a change from positive to negative Weiss constant theta sub W that is mainly due to the [M-O sub 6] octahe...

  16. Mo-Isotopes in the Oceans and a Case Study From the Black Sea

    Science.gov (United States)

    Siebert, C.; Nagler, T. F.; Boettcher, M.; Kramers, J. D.

    2002-12-01

    Because of an increasing number of Mo isotope fractionation data, the geochemical cycle of Mo especially in the recent oceans is now better understood. Data presented here were determined using a Nu instruments MC-ICPMS and double spike techniques (external reproducibility generally below 0.1 permil (2s.d.) on 98Mo/95Mo). Mo isotopes are homogenous in the oceans (+2.3 delta 98Mo/95Mo relative to JMC in-house standard) at present day resolution. All data are therefore given in delta notation relative to Mean Ocean water Mo (MOMO). Mo-Sources: Continental rocks, assumed to represent the riverrhine input, show a narrow range of Mo isotope compositions (-2.0 to -2.3 permil) close to the in-house standard solution. Oxic Mo-sinks: Pelagic sediments and recent Fe-Mn crust surfaces show lighter Mo isotope compositions (-2.7 to -3.2 permil). In addition, to depth profiles through thick sections of Fe-Mn crusts also yield uniform Mo isotope compositions (average of -2.9 and -3.2) over the last 60Ma implying a homogenous isotope composition in ocean water over this time period. This makes Mo different from other oceanic proxies since the large variations in environmental parameters seem to have not affected Mo. We explain the observed general offset of about 3 permil from ocean water with an equilibrium fractionation between major and minor Mo species in the water column, of which the latter are lighter and can be scavenged more efficiantly due to higher coordination numbers. Suboxic Mo-sinks: The balancing heavier Mo isotope composition with respect to the input can be found in recent suboxic sediments from open ocean basins, which display variable values but are all heavier than the input (-0.7 to -1.6 permil). The influence of Low-T hydrothermal activity on the Mo isotope budget in the oceans is still to be tested. Mo isotopes in the Black-Sea: Because of its limited water exchange with the open oceans, the high surface freshwater content (1/3) and its widespread bottom

  17. Relationship Between Soil Properties and Different Fractions of Soil Hg

    Institute of Scientific and Technical Information of China (English)

    WUHONGTAO; YUGUIFEN; 等

    2001-01-01

    Correlation and path analysis methods were used to study the relationship between soil properties and the distribution of different soil Hg fractions with nine representative soils from Chongqing,China,Results showed that clay(<2m) could increase water-soluble Hg(r=0.700*).Soil organic matter (OM) could enhance the increase of elemental Hg(r=0.674*),The higher the base saturation percentage (BSP) ,the more the residual Hg(R=0.684*) .Organic Hg,the sum of said-soluble organic He and alkali-soluble Hg,was positively affected by silt(2-20μm)but negatively affected by pH,with the direct path coefficients amounting to 1.0487 and 0.5121,respectively .The positive effect of OM and negative effect of BSP on organic Hg were the most significant ,with the direct path coefficients being 0.7614 and -0.8527,respectively. The indirect effect of clay(<2μm) iva BSP (path coefficient=0.4186) was the highest,showing that the real influencing factor in the effect of clay(<2μm) via BSP (path coefficient=0.4186) was the highest,showing that the real influencing factor in the effect of clay(<2μm) on acid-soluble organic Hw was BSP.since the available Hg fraction,water-soluble Hg,was positively affected by soil clay content,and the quite immobile and not bioavailable residual Hg by soil BSP,suitable reduction of clay content and increase of BSP would be of much help to reduce the Hg availability and Hg activity in Hg-contaminated soils.

  18. Crystalline structure, and magnetic and magneto-optical properties of MnSbBi thin films

    CERN Document Server

    Kang, K

    2001-01-01

    the c-axis texture and the saturation magnetisation due to less segregation of the non-magnetic phase in the annealed films. Using a thin Sb seed layer in Mn/Sb/Bi// films also results in an increase in both the c-axis texture and the saturation magnetisation. Decreasing the layer thicknesses in Mn/Bi/Sb// films results in a decrease in the grain size. By depositing the Sb layer first in Pt/Mn/Sb// and Co/Mn/Sb// films, the perpendicular c-axis texture can be kept before and after annealing. Computer simulation was carried out to investigate the relationship between the crystal structure and the magnetic properties before and after annealing. Comparing optical and MO properties of annealed Mn/Sb/Bi// and Mn/Sb// films suggests a possible origin of the peaks in Kerr spectra caused by adding Bi. This thesis reports work carried out to investigate some aspects of the crystal structure, and magnetic and magneto-optical (MO) properties in thin films of the Mn-Sb system. Reports of interesting properties and the po...

  19. Determination of the compositeness of resonances from decays: The case of the Bs<mn>0mn> stretchy='false'>→mo>J stretchy='false'>/mo>ψf>1mn> stretchy='false'>(mo>>1285mn> stretchy='false'>)mo>

    Energy Technology Data Exchange (ETDEWEB)

    Molina, R.; Döring, M.; Oset, E.

    2016-06-01

    We develop a method to measure the amount of compositeness of a resonance, mostly made as a bound state of two hadrons, by simultaneously measuring the rate of production of the resonance and the mass distribution of the two hadrons close to threshold. By using different methods of analysis we conclude that the method allows one to extract the value of 1-Z with about $0.1$ of uncertainty. The method is applied to the case of the $\\bar B^0_s \\to J/\\psi f_1(1285)$ decay, by looking at the resonance production and the mass distribution of $K \\bar K^*$.

  20. Double Double Cation Order in the High-Pressure Perovskites MnRMnSbO6.

    Science.gov (United States)

    Solana-Madruga, Elena; Arévalo-López, Ángel M; Dos Santos-García, Antonio J; Urones-Garrote, Esteban; Ávila-Brande, David; Sáez-Puche, Regino; Attfield, J Paul

    2016-08-01

    Cation ordering in ABO3 perovskites adds to their chemical variety and can lead to properties such as ferrimagnetism and magnetoresistance in Sr2 FeMoO6 . Through high-pressure and high-temperature synthesis, a new type of "double double perovskite" structure has been discovered in the family MnRMnSbO6 (R=La, Pr, Nd, Sm). This tetragonal structure has a 1:1 order of cations on both A and B sites, with A-site Mn(2+) and R(3+) cations ordered in columns and Mn(2+) and Sb(5+) having rock salt order on the B sites. The MnRMnSbO6 double double perovskites are ferrimagnetic at low temperatures with additional spin-reorientation transitions. The ordering direction of ferrimagnetic Mn spins in MnNdMnSbO6 changes from parallel to [001] below TC =76 K to perpendicular below the reorientation transition at 42 K at which Nd moments also order. Smaller rare earths lead to conventional monoclinic double perovskites (MnR)MnSbO6 for Eu and Gd.

  1. Oxidative stress in MeHg-induced neurotoxicity

    Energy Technology Data Exchange (ETDEWEB)

    Farina, Marcelo, E-mail: farina@ccb.ufsc.br [Departamento de Bioquimica, Centro de Ciencias Biologicas, Universidade Federal de Santa Catarina, Florianopolis, SC (Brazil); Aschner, Michael [Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN (United States); Department of Pharmacology, Vanderbilt University Medical Center, Nashville, TN (United States); Rocha, Joao B.T., E-mail: jbtrocha@yahoo.com.br [Departamento de Quimica, Centro de Ciencias Naturais e Exatas, Universidade Federal de Santa Maria, Santa Maria, RS (Brazil)

    2011-11-15

    Methylmercury (MeHg) is an environmental toxicant that leads to long-lasting neurological and developmental deficits in animals and humans. Although the molecular mechanisms mediating MeHg-induced neurotoxicity are not completely understood, several lines of evidence indicate that oxidative stress represents a critical event related to the neurotoxic effects elicited by this toxicant. The objective of this review is to summarize and discuss data from experimental and epidemiological studies that have been important in clarifying the molecular events which mediate MeHg-induced oxidative damage and, consequently, toxicity. Although unanswered questions remain, the electrophilic properties of MeHg and its ability to oxidize thiols have been reported to play decisive roles to the oxidative consequences observed after MeHg exposure. However, a close examination of the relationship between low levels of MeHg necessary to induce oxidative stress and the high amounts of sulfhydryl-containing antioxidants in mammalian cells (e.g., glutathione) have led to the hypothesis that nucleophilic groups with extremely high affinities for MeHg (e.g., selenols) might represent primary targets in MeHg-induced oxidative stress. Indeed, the inhibition of antioxidant selenoproteins during MeHg poisoning in experimental animals has corroborated this hypothesis. The levels of different reactive species (superoxide anion, hydrogen peroxide and nitric oxide) have been reported to be increased in MeHg-exposed systems, and the mechanisms concerning these increments seem to involve a complex sequence of cascading molecular events, such as mitochondrial dysfunction, excitotoxicity, intracellular calcium dyshomeostasis and decreased antioxidant capacity. This review also discusses potential therapeutic strategies to counteract MeHg-induced toxicity and oxidative stress, emphasizing the use of organic selenocompounds, which generally present higher affinity for MeHg when compared to the classically

  2. Modeling interactions of Hg(II) and bauxitic soils.

    Science.gov (United States)

    Weerasooriya, Rohan; Tobschall, Heinz J; Bandara, Atula

    2007-11-01

    The adsorptive interactions of Hg(II) with gibbsite-rich soils (hereafter SOIL-g) were modeled by 1-pK surface complexation theory using charge distribution multi-site ion competition model (CD MUSIC) incorporating basic Stern layer model (BSM) to account for electrostatic effects. The model calibrations were performed for the experimental data of synthetic gibbsite-Hg(II) adsorption. When [NaNO(3)] > or = 0.01M, the Hg(II) adsorption density values, of gibbsite, Gamma(Hg(II)), showed a negligible variation with ionic strength. However, Gamma(Hg(II)) values show a marked variation with the [Cl(-)]. When [Cl(-)] > or = 0.01M, the Gamma(Hg(II)) values showed a significant reduction with the pH. The Hg(II) adsorption behavior in NaNO(3) was modeled assuming homogeneous solid surface. The introduction of high affinity sites, i.e., >Al(s)OH at a low concentration (typically about 0.045 sites nm(-2)) is required to model Hg(II) adsorption in NaCl. According to IR spectroscopic data, the bauxitic soil (SOIL-g) is characterized by gibbsite and bayerite. These mineral phases were not treated discretely in modeling of Hg(II) and soil interactions. The CD MUSIC/BSM model combination can be used to model Hg(II) adsorption on bauxitic soil. The role of organic matter seems to play a role on Hg(II) binding when pH>8. The Hg(II) adsorption in the presence of excess Cl(-) ions required the selection of high affinity sites in modeling.

  3. Lithography process for patterning HgI2 photonic devices

    Science.gov (United States)

    Mescher, Mark J.; James, Ralph B.; Hermon, Haim

    2004-11-23

    A photolithographic process forms patterns on HgI.sub.2 surfaces and defines metal sublimation masks and electrodes to substantially improve device performance by increasing the realizable design space. Techniques for smoothing HgI.sub.2 surfaces and for producing trenches in HgI.sub.2 are provided. A sublimation process is described which produces etched-trench devices with enhanced electron-transport-only behavior.

  4. Epitaxial growth of HgTe by a MOVPE process

    Energy Technology Data Exchange (ETDEWEB)

    Irvine, S.J.C.; Mullin, J.B.; Royle, A. (Royal Signals and Radar Establishment, Malvern (UK))

    1982-03-01

    Epitaxial layers of HgTe have been grown onto insulating CdTe substrates by the pyrolysis of (C/sub 2/H/sub 5/)/sub 2/Te in the presence of Hg vapour using a H/sub 2/ flow system. Temperature-dependent Hall effect and conductivity measurements have shown that the electrical properties of the layers are comparable with good quality bulk HgTe.

  5. First principles study of a new half-metallic ferrimagnets Mn{sub 2}-based full Heusler compounds: Mn{sub 2}ZrSi and Mn{sub 2}ZrGe

    Energy Technology Data Exchange (ETDEWEB)

    Abada, A. [Laboratoire d’études physico-chimiques, Université Dr Moulay Tahar, Saida 20000 (Algeria); Amara, K., E-mail: kamaraphy@gmail.com [Laboratoire d’études physico-chimiques, Université Dr Moulay Tahar, Saida 20000 (Algeria); Hiadsi, S. [Département de Génie Physique, Université d’Oran des sciences et de la technologie Mohamed Boudiaf (Algeria); Amrani, B. [Département de Physique, Université d’Oran Es-Senia, Oran 31000 (Algeria)

    2015-08-15

    Half-metallic properties of new predicted Mn{sub 2}-based full Heusler alloys Mn{sub 2}ZrSi and Mn{sub 2}ZrGe have been studied by first-principles full-potential linearized augmented plane wave plus local orbital (FP-LAPW+lo) method based on density functional theory (DFT). Our investigation is focused on the structural, elastic, electronic and magnetic properties of these compounds. The AlCu{sub 2}Mn-type structure is found to be energetically more favorable than the CuHg{sub 2}Ti-type structure for both compounds and are half-metallic ferrimagnets (HMFIs) with total magnetic moments of 2.000µ{sub B} per formula unit, well consistent with Slater–Pauling rule (M{sub tot}=(24–Z{sub tot})µ{sub B}). Calculations show that both the alloys have an indirect band gaps, in the majority-spin channel, with values of 0.505 eV and 0.278 eV for Mn{sub 2}ZrSi and Mn{sub 2}ZrGe, respectively. It was found that Mn{sub 2}ZrSi and Mn{sub 2}ZrGe preserved their half-metallicity for lattice constants range of 5.85–6.38 Å and 6.05–6.38 Å, respectively, and kept a 100% of spin polarization at the Fermi level. Moreover, the calculated formation energies and elastic constants confirm that these compounds are stable chemically and mechanically, and the good crystallographic compatibility with the lattice of semiconductors used industrially makes them promising magnetic materials in spintronic applications. - Highlights: • For Mn{sub 2}ZrZ (Z=Si, Ge) the AlCu{sub 2}Mn-type structure is more favorable than the CuHg{sub 2}Ti-type. • The calculated elastic constants confirm their mechanical stability. • Their negative estimated formation energies means they can be synthesized. • Their lattice constants match well with those of many semiconductor substrates. • They are predicted to be true half-metallic ferrimagnets. • The band gaps of Mn{sub 2}ZrSi~0.51 eV and Mn{sub 2}ZrGe~0.28 eV are indirect along, the Γ–X.

  6. Experiments with a New 201Hg+ Ion Clock

    Science.gov (United States)

    Burt, E. A.; Taghavi-Larigani, S.; Lea, S. N.; Prestage, J. D.; Tjoelker, R. L.

    2009-04-01

    In this paper we describe a new clock based on 201Hg+. All previous mercury ion clocks have been based on 199Hg+. We have recently completed construction of the 201Hg+ clock and will describe modifications to the design of our existing 199Hg+ clocks to accommodate the new isotope. We will also describe initial spectroscopic measurements of the hyperfine manifold, and possible future experiments. One experiment could place a limit on variations in the strong interaction fundamental constant ratio mq/ΛQCD.REFID="9789812838223_0043FN001">

  7. PENCEMARAN LOGAM BERAT MERKURI (Hg PADA AIRTANAH

    Directory of Open Access Journals (Sweden)

    Thomas Triadi Putranto

    2012-02-01

    Full Text Available The earth consists largely of water because the land area is smaller than the ocean. Human beings on this earthcan not escape the need for water. Water is the main requirement for the process of life on the earth.Relatively clean water that is coveted by men, whether for purposes of daily life, for industrial purposes, for thecleanliness of city sanitation, as well as for agricultural purposes and so forth. Heavy metal pollution is a veryserious issue to be handled, because of adverse environmental and ecosystem in general. Heavy metallic elementis the element which has a density of more than 5 gr/cm3. Hg has a density of 13.55 gr/cm3. Disaster is anoutbreak of Minamata mercury poisoning in people who eat fish contaminated by mercury in Minamata Japan,and this event is known as Minamata Disease. Efforts to tackle the heavy metal pollution can actually be doneusing a chemical process or by microorganism such as microbes and bacteria.

  8. Hg-coordination studies of oligopeptides containing cysteine, histidine and tyrosine by $^{199m}$Hg-TDPAC

    CERN Document Server

    Ctortecka, B; Mallion, S; Butz, T; Hoffmann, R

    1999-01-01

    In order to study the interaction of histidine- and tyrosine- containing peptide chains with Hg(II), the nuclear quadrupole interaction (NQI) of /sup 199m/Hg in the Hg complexes of the oligopeptides alanyl-alanyl-histidyl-alanyl-alanine-amid (AAHAA-NH /sub 2/) and alanyl-alanyl-tyrosyl-alanyl-alanine-amid (AAYAA-NH/sub 2/) was determined by time differential perturbed angular correlation and is compared with previous data on alanyl-alanyl-cysteyl-alanyl- alanyl (AACAA-OH). The /sup 199m/Hg-NQIs depend on the oligopeptide to Hg(II) stoichiometry and indicate that two-fold and four-fold coordinations occur for the bound Hg(II). (12 refs).

  9. Effects of AlMnCa and AlMnFe Alloys on Deoxidization of Low Carbon and Low Silicon Aluminum Killed Steels

    Institute of Scientific and Technical Information of China (English)

    ZHAN Dong-ping; ZHANG Hui-shu; JIANG Zhou-hua

    2008-01-01

    To confirm the effects of AlMnCa and AIMnFe alloys on the deoxidization and modification of Al2O3 inclu-sions, experiments of 4-heat low carbon and low silicon aluminum killed steels deoxidized by AlMnCa and AlMnFe alloys were done in a MoSi2 furnace at 1 873 K. It is found that the 1# A1MnCa alloy has the best ability of deoxidi-zation and modification of Al2 O3 inclusions than 2# A1MnCa and A1MnFe alloys. Steel A deoxidized by 1# AlMnCa alloy has the lowest total oxygen content in the terminal steel, which is 37 × 10-6. Most of the inclusions in the steel deoxidized by 1# AIMnCa alloy are spherical CaO-containing compound inclusions, and 89. 1% of them are smaller than 10 μm. The diameter of the inclusion bigger than 50 μm is not found in the final steels deoxidized by AlMnCa alloys. Whereas, for the steels deoxidized by AlMnFe alloys, most inclusions in the terminal steel are Al2O3 or Al2O3-MnO inclusions, and a few of them are spherical, and only 76. 8% of them are smaller than 10 μm. Some in-clusions bigger than 50 μm are found in the steel D deoxidized by AlMnFe alloy.

  10. Coumarin-based fluorescence hybrid silica material used for selective detection and absorption of Hg2+ in aqueous media

    Science.gov (United States)

    Meng, Qingtao; Jia, Hongmin; Wang, Cuiping; Zhao, Hongbin; Lu, Gonghao; Hu, Zhizhi; Zhang, Zhiqiang; Duan, Chunying

    2014-11-01

    An inorganic-organic hybrid fluorescence material (C-SBA-15) was prepared by covalent immobilization of a coumarin derivative within the channels of SBA-15. The characterization results of XRD, TEM micrographs, FT-IR and UV-vis demonstrate that coumarin is successfully grafted onto the inner surface of SBA-15 and its organized structure is preserved. C-SBA-15 can detect Hg2+ with high selectivity to Pb2+, Zn2+, Cu2+, Mn2+, Cd2+, Co2+, Ag+, Fe3+, Ni2+, K+, Na+, Ca2+, Mg2+ and Li+ in water. Furthermore, the fluorogenical response is reversible by treating with EDTA and do not vary over a broad pH range (5.0-10.5). C-SBA-15 features more outstanding absorbing capacity for Hg2+ among other HTM ions in water.

  11. Constant Molybdenum Isotope Composition of Ocean Water and Fe-Mn crusts for the Last 70 Myr

    Science.gov (United States)

    Siebert, C.; Nagler, T. F.; von Blankenburg, F.; Kramers, J. D.

    2001-12-01

    In the relatively new field of heavy stable isotope geochemistry, molybdenum (Mo) is one of the very promising elements. Molybdenum is a redox-sensitive trace metal. Isotope fractionation during terrestrial processes such as low-temperature redox transitions, chemical weathering, changes in the composition of the atmosphere, hydrothermal activity and sedimentary cycling is likely. Molybdenum is also an essential element for biological nitrogen fixation. Therefore, biogeochemical Mo isotope fractionation is also probable. The oceans represent an important terrestrial Mo reservoir. Dissolved concentrations in seawater are relatively high (0.01 ppm). The global ocean residence time is corresponding high with 800 kyr. The aim of this study is to characterise the principle present day oceanic Mo reservoirs and their changes with time. Molybdenum isotopic compositions were determined precisely using a Nu instruments MC-ICP-MS. Instrumental and laboratory mass fractionation is separated from natural mass dependent fractionation by addition of a molybdenum double spike prior to chemical separation (Siebert et al., 2001). The external standard reproducibility is at or below 0.1 per mil for the 98Mo/95Mo ratio (2s.d.). We analysed ocean water samples from the Atlantic (n=3, 0m-2400m depth), the Pacific and the Indian Ocean (deep water). These yield a homogeneous Mo isotopic composition as would be expexted from the long residence time of Mo in the oceans. Ocean water has the heaviest Mo isotopic composition measured to date (+2.3 per mil on the 98Mo/95Mo ratio relative to a Johnson Mattey ICP standard solution, lot 602332B). In view of the homogeneous ocean water ratios, we propose the use of present day ocean water as an reference standard (Mean Ocean Molybdenum: MOMO). Significantly lighter compositions from -2.7 to -3.1 per mil on the 98Mo/95Mo ratio relative to MOMO were determined for six Fe-Mn crust surface layers. Pelagic clay (-2.7 per mil) and clastic sediments (-2

  12. Energy levels of 56Mn

    DEFF Research Database (Denmark)

    Van Assche, P. H. M.; Baader, H. A.; Koch, H. R.

    1971-01-01

    The low-energy spectrum of the 55Mn(n,γ)56 Mn reaction has been studied with a γ-diffraction spectrometer. These data allowed the construction of a level scheme for 56Mn with two previously unobserved doublets. High-energy γ-transitions to the low-energy states have been measured for different...

  13. Energy dependence of the prompt γ -ray emission from the <mo>(mo>d<mo>,p)> -induced fission of U<mo>*>234mn> and Pu<mo>*>240mn>

    Energy Technology Data Exchange (ETDEWEB)

    Rose, S. J.; Zeiser, F.; Wilson, J. N.; Oberstedt, A.; Oberstedt, S.; Siem, S.; Tveten, G. M.; Bernstein, L. A.; Bleuel, D. L.; Brown, J. A.; Crespo Campo, L.; Giacoppo, F.; Görgen, A.; Guttormsen, M.; Hadyńska, K.; Hafreager, A.; Hagen, T. W.; Klintefjord, M.; Laplace, T. A.; Larsen, A. C.; Renstrøm, T.; Sahin, E.; Schmitt, C.; Tornyi, T. G.; Wiedeking, M.

    2017-07-01

    Prompt-fission γ rays are responsible for approximately 5% of the total energy released in fission, and therefore important to understand when modeling nuclear reactors. In this work we present prompt γ -ray emission characteristics in fission as a function of the nuclear excitation energy of the fissioning system. Emitted γ -ray spectra were measured, and γ -ray multiplicities and average and total γ energies per fission were determined for the 233 U ( d , p f ) reaction for excitation energies between 4.8 and 10 MeV, and for the 239 Pu ( d , p f ) reaction between 4.5 and 9 MeV. The spectral characteristics show no significant change as a function of excitation energy above the fission barrier, despite the fact that an extra ~ 5 MeV of energy is potentially available in the excited fragments for γ decay. The measured results are compared with model calculations made for prompt γ -ray emission with the fission model code gef. Further comparison with previously obtained results from thermal neutron induced fission is made to characterize possible differences arising from using the surrogate ( d , p ) reaction.

  14. Effects of Mo on the Precipitation Behaviors in High-Nitrogen Austenitic Stainless Steels

    Institute of Scientific and Technical Information of China (English)

    Feng Shi; Yang Qi; Chunming Liu

    2011-01-01

    Precipitation behaviors of Fe-18Cr-18Mn-0.63N and Fe-18Cr-18Mn-2Mo-0.69N high-nitrogen austenitic stainless steels during isothermally aging at 850℃ have been investigated by optical microscopy (OM), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray diffraction (XRD). The experimental results show that precipitation displays a discontinuous cellular way and the precipitates are identified as Cr2N in Fe-18Cr-18Mn-0.63N steel. The addition of Mo makes precipitation occur not only at the grain boundary but also inside the grain and precipitation also displays discontinuous cellular way. The precipitates at the grain boundary and in the cell are both identified as G2N phase and χ phase and the precipitates inside the grain are identified as χ phase in Fe-18Cr-18Mn-2Mo-0.69N steel. The nucleations of χ phase and Cr2N phase at the grain boundary are both governed by the diffusion of Cr atoms. The formation and growth of χ phase inside the grain are induced by the impoverishment of N atoms with increasing aging time.

  15. Modification-free and N-acetyl-L-cysteine-induced colorimetric response of AuNPs: A mechanistic study and sensitive Hg(2+) detection.

    Science.gov (United States)

    Tang, Jie; Wu, Peng; Hou, Xiandeng; Xu, Kailai

    2016-10-01

    A facile yet sensitive and selective method was proposed for Hg(2+) detection based on N-acetyl-L-cysteine(NAC)-induced colorimetric response of AuNPs. The proposed method can be easily performed by introducing the premixing of NAC and Hg(2+) into as-prepared citrate-capped AuNPs solution. A combination of experimental and theoretical studies was applied to illustrate the mechanism of this AuNPs colorimetric system. The strong interaction of NAC and AuNPs through Au-S bond could lead to the aggregation of AuNPs, but the formation of NAC-Hg-NAC complex decreased the affinity between NAC and AuNPs and resulted in an anti-aggregation effect. Therefore, the color of the AuNPs solution would progress from purple to red with the increase of Hg(2+) concentration. The proposed method had a high sensitivity with a limit of detection of 9.9nM. Coexistent metal ions, including Cd(2+), Mn(2+), Al(3+), Ag(+), K(+), Mg(2+), Ca(2+), Cr(3+), Cu(2+), Fe(3+), Pb(2+), Ni(2+) and Zn(2+), did not interfere with the detection of Hg(2+). This method can be used to monitor Hg(2+) in tap water.

  16. SO2/Hg removal from flue gas by dry FGD

    Institute of Scientific and Technical Information of China (English)

    Wang Fan; Wang Hongmei; Zhang Fan; Zhu Jinwei; Tian Gang; Liu Yu; Mao Jixian

    2012-01-01

    To study the mechanism of SO2 and Hg removal from flue gas,an experimental packed bed reactor was designed to simulate the dry FGD,where a mixture of lime and fly ash in ratio 1∶3 w/w was used as the SO2 and Hg sorbent,and steam at temperature of 100 ℃ was applied for activation of the sorbent,while the activation time set to 20 min.The experimental factors including the SO2/Hg sorbent characteristics,50% breakthrough time for SO2/Hg removal,sorbent packed bed depth and reaction temperature were investigated.The experimental results show that after steam activation,the BET specific surface area and specific pore volume increased from 37.8 to 45.5 m2/g and from 0.42 to 0.51 cm3/g,respectively.With activation of the sorbent by steam,the 50% breakthrough times of SO2 and Hg removal increased from 34 to 42 min and from 23 to 45 min,respectively.When the packed bed depth was increased from 5 to 25 mm,the 50% breakthrough times for Hg and SO2 removal increased from 12 to 52 min and from 6 to 47 min,respectively.With the increase of the reaction temperature,the 50% breakthrough of SO2/Hg removal decreased accordingly.Steam activation can efficiently improve SO2/Hg removal simultaneously.

  17. Manganese-mediated ferromagnetism in La2Fe1-Mn2Cr1-O6 perovskite oxides

    Indian Academy of Sciences (India)

    R M Tiwari; Mrudul Gadhvi; Abanti Nag; N Y Vasanthacharya; J Gopalakrishnan

    2010-07-01

    We have investigated the structure and magnetic properties of the perovskite oxides of the formula La2Fe1-Mn2Cr1-O6 (0 < < 1.0). For 0 < ≤ 0.5, the members adopt the orthorhombic (Pbnm) structure, where the transition metal atoms are disordered at the 4b sites and the MO6 (M = Fe, Mn, Cr) octahedra become increasingly distorted with increasing . For 0.65 ≤ < 1.0, the members adopt the rhombohedral (R-3c) structure that is similar to LaMnO3+ ( ≥ 0.1) where the MO6 octahedra are undistorted. While the magnetic properties of the latter series are largely similar to the parent LaMnO3+ arising from the double-exchange (DE) between mixed valent MnIII/MnIV, the magnetic properties of the orthorhombic members show a distinct (albeit weak) ferromagnetism (C ∼ 200 K) that seems to arise from a MnIII-mediated superexchange (SE) between FeIII/CrIII in the disordered perovskite structure containing FeIII, MnIII and CrIII.

  18. Mn(II) oxidation by an ascomycete fungus is linked to superoxide production during asexual reproduction

    Energy Technology Data Exchange (ETDEWEB)

    Hansel, C. M.; Zeiner, C. A.; Santelli, C. M.; Webb, S. M.

    2012-07-16

    Manganese (Mn) oxides are among the most reactive minerals within the environment, where they control the bioavailability of carbon, nutrients, and numerous metals. Although the ability of microorganisms to oxidize Mn(II) to Mn(III/IV) oxides is scattered throughout the bacterial and fungal domains of life, the mechanism and physiological basis for Mn(II) oxidation remains an enigma. Here, we use a combination of compound-specific chemical assays, microspectroscopy, and electron microscopy to show that a common Ascomycete filamentous fungus, Stilbella aciculosa, oxidizes Mn(II) to Mn oxides by producing extracellular superoxide during cell differentiation. The reactive Mn oxide phase birnessite and the reactive oxygen species superoxide and hydrogen peroxide are colocalized at the base of asexual reproductive structures. Mn oxide formation is not observed in the presence of superoxide scavengers (e.g., Cu) and inhibitors of NADPH oxidases (e.g., diphenylene iodonium chloride), enzymes responsible for superoxide production and cell differentiation in fungi. Considering the recent identification of Mn(II) oxidation by NADH oxidase-based superoxide production by a common marine bacterium (Roseobacter sp.), these results introduce a surprising homology between some prokaryotic and eukaryotic organisms in the mechanisms responsible for Mn(II) oxidation, where oxidation appears to be a side reaction of extracellular superoxide production. Finally, given the versatility of superoxide as a redox reactant and the widespread ability of fungi to produce superoxide, this microbial extracellular superoxide production may play a central role in the cycling and bioavailability of metals (e.g., Hg, Fe, Mn) and carbon in natural systems.

  19. Mn(II) oxidation by an ascomycete fungus is linked to superoxide production during asexual reproduction.

    Science.gov (United States)

    Hansel, Colleen M; Zeiner, Carolyn A; Santelli, Cara M; Webb, Samuel M

    2012-07-31

    Manganese (Mn) oxides are among the most reactive minerals within the environment, where they control the bioavailability of carbon, nutrients, and numerous metals. Although the ability of microorganisms to oxidize Mn(II) to Mn(III/IV) oxides is scattered throughout the bacterial and fungal domains of life, the mechanism and physiological basis for Mn(II) oxidation remains an enigma. Here, we use a combination of compound-specific chemical assays, microspectroscopy, and electron microscopy to show that a common Ascomycete filamentous fungus, Stilbella aciculosa, oxidizes Mn(II) to Mn oxides by producing extracellular superoxide during cell differentiation. The reactive Mn oxide phase birnessite and the reactive oxygen species superoxide and hydrogen peroxide are colocalized at the base of asexual reproductive structures. Mn oxide formation is not observed in the presence of superoxide scavengers (e.g., Cu) and inhibitors of NADPH oxidases (e.g., diphenylene iodonium chloride), enzymes responsible for superoxide production and cell differentiation in fungi. Considering the recent identification of Mn(II) oxidation by NADH oxidase-based superoxide production by a common marine bacterium (Roseobacter sp.), these results introduce a surprising homology between some prokaryotic and eukaryotic organisms in the mechanisms responsible for Mn(II) oxidation, where oxidation appears to be a side reaction of extracellular superoxide production. Given the versatility of superoxide as a redox reactant and the widespread ability of fungi to produce superoxide, this microbial extracellular superoxide production may play a central role in the cycling and bioavailability of metals (e.g., Hg, Fe, Mn) and carbon in natural systems.

  20. Pencemaran air raksa (Hg sebagai dampak pengolahan bijih emas di Sungai Ciliunggunung, Waluran, Kabupaten Sukabumi

    Directory of Open Access Journals (Sweden)

    Widodo Widodo

    2014-06-01

    Full Text Available http://dx.doi.org/10.17014/ijog.vol3no3.20083Gold ore mining at Waluran Subregency, Sukabumi Regency was carried out by an underground mining method, and only rock that contains high enough gold ore would be taken (selective mining. The gold ore from the mining was processed with a direct amalgamation method, so it produced low gold concentrate, but the concentrate of mercury discarded to the river was high enough. Monitoring result of water and sedimentation in Ciliunggunung River in 2004, showed that the river was contamined by mercury (Hg, and the contamination was above the value limit. This happened especially in August 2005 where the Hg content was about 0.218 mg/l on the Ciliunggunung River in CLG.07. The chemical analysis result of heavy metals for the water of the Ciliunggunung River in CLG.07 was known to contain Fe above the standard drinking water criteria, meanwhile Mn, Cu, Pb, and As were still under the maximum drinking water criteria value. To decrease the mercury contamination, it is suggested the process of gold ore from the amalgamation direct method to be changed to the amalgamation indirect method. The indirect gold ore amalgamation process consists of: removing fine particles by washing, grinding ore, and the amalgamation phase. The total impact of the indirect amalgamation method will increase the tying of gold by mercury, so the losing of mercury will be decreased and the gain of gold will be optimum.  

  1. Adjusting band gap and charge transfer of organometallic complex adsorbed on MoS2 monolayer using vertical electric-field: a first-principles investigation

    Science.gov (United States)

    Bui, Viet Q.; Le, Hung M.; Kawazoe, Yoshiyuki; Kim, Yongho

    2017-01-01

    In this paper, we propose the use of benzene (Bz) to cover the active site on top of a transition metal atom (Cr/Mn/Fe) adsorbed on the MoS2 monolayer. Stable configurations of adatom on the MoS2 surface were predicted using first-principles calculations and their electronic, magnetic properties were investigated. In addition, the influence of vertical electric field on the electronic band structures of the systems was carefully examined. Analyzing the adsorption energies of transition metals given by the PBE calculations, we found that the benzene molecule stabilized the binding of Cr and Mn on the MoS2 surface, but destabilized the Fe binding by approximately 33% of adsorption energy. The attachment of benzene caused modifications on the total magnetizations of the Cr-MoS2 and Mn-MoS2 structures. The Bz-Mn@MoS2 structure was found to exhibit half-metallicity with 100% spin polarization at the Fermi level. The influence of various degrees of vertical electric field was shown to produce a tensile stress, which altered the lattice parameters and led to band gap narrowing and dramatic shifts of the Fermi level.

  2. Earthworm casts as a sampling medium – a case study from highly contaminated Hg roasting site Pšenk (Idrija area, Slovenia

    Directory of Open Access Journals (Sweden)

    Tamara Teršič

    2013-12-01

    Full Text Available In this study an interesting sampling medium - earthworm casts was examined in a highly Hg contaminated area. Enrichment factor (EF has been applied to assess elevated concentrations of analyzed elements in earthworm casts and to determine elevated concentrations of these elements in soils and casts with regard to European average concentrations in topsoil. In a previous study (Teršič & Gosar, 2012 it was shown that Hg contents and dispersion in casts from studied roasting site are comparable to those in soil, which indicates that soil contamination is substantially reflected in contamination of earthworm casts. Therefore the comparison between elemental concentrations in earthworm casts and soil was investigated with the intention to assess the reflection of possible soil contamination in casts. Besides Hg contamination, elevated concentrations of As, Ca, Cd, Mo, Pb and U were also determined in earthworm casts. The calculated EFs show moderate enrichment of casts with Ca, Sr and P and minimal enrichment with Mg, Zn and Cu. Cast, SOM (surface organic matter rich soil layer and soil enrichments with regard to the European averages show extreme enrichment of all studied media with Hg, followed by significant enrichment with Mo and Cd and moderate enrichment with As. Spatial distributions of analyzed elements in casts mostly show similar pattern as in soil, however, because of the different nature of different earthworm species and specific properties of different elements, the data about cast contamination can only serve as an approximate prediction about the dispersion and distribution of contaminant in soil.

  3. Hg localisation in Tillandsia usneoides L. (Bromeliaceae), an atmospheric biomonitor

    Energy Technology Data Exchange (ETDEWEB)

    Filho, G.M.A. [Instituto de Pesquisas Jardim Botanico do Rio de Janeiro (Brazil). Programa Zona Costeira; Andrade, L.R.; Farina, M. [Cidade Universitaria, Rio de Janeiro (Brazil). Instituto de Ciencias Biomedicas, Departamento de Anatomia; Malm, O. [Cidade Universitaria, Rio de Janeiro (Brazil). Instituto de Biofisica Carlos Chagas Filho, Laboratorio de Radioisotopos Eduardo Penna Franca

    2002-07-01

    The Spanish moss, Tillandsia usneoides, has been applied as an atmospheric biomonitor of Hg contamination, although the mechanism of metal plant accumulation has not been understood until now. In the present work, analytical scanning electron microscopy (SEM) was used to localize Hg in T. usneoides exposed to a Hg-air-contaminated area during 15 days. After this period, Hg was determined by the flow injection mercury system, and plants were prepared for SEM observation and energy-dispersive X-ray analysis. A concentration of 2702{+-}318{mu}g Hgg{sup -1} was determined in exposed plants. The presented microanalytical results demonstrated that Hg was partly associated with atmospheric particles deposited upon the plant surface, but it was highly absorbed by the scales, stem and leaves surfaces and less absorbed by epidermal cells of T. usneoides. No Hg was detected in mesophyll parenchyma or in vascular system cells. The great surface adsorption area provided by the scales, in addition to the characteristics of T. usneoides morphology, especially of the node region, are suggested to confer the great capability of T. usneoides in Hg holding. (author)

  4. Austenite Formation from Martensite in a 13Cr6Ni2Mo Supermartensitic Stainless Steel

    OpenAIRE

    2016-01-01

    The influence of austenitization treatment of a 13Cr6Ni2Mo supermartensitic stainless steel (X2CrNiMoV13-5-2) on austenite formation during reheating and on the fraction of austenite retained after tempering treatment is measured and analyzed. The results show the formation of austenite in two stages. This is probably due to inhomogeneous distribution of the austenite-stabilizing elements Ni and Mn, resulting from their slow diffusion from martensite into austenite and carbide and nitride dis...

  5. Mn bioavailability by polarized Caco-2 cells: comparison between Mn gluconate and Mn oxyprolinate

    Directory of Open Access Journals (Sweden)

    Fulgenzi Alessandro

    2011-07-01

    Full Text Available Abstract Background Micronutrient inadequate intake is responsible of pathological deficiencies and there is a need of assessing the effectiveness of metal supplementation, frequently proposed to rebalance poor diets. Manganese (Mn is present in many enzymatic intracellular systems crucial for the regulation of cell metabolism, and is contained in commercially available metal supplements. Methods We compared the effects of two different commercial Mn forms, gluconate (MnGluc and oxyprolinate (MnOxP. For this purpose we used the polarized Caco-2 cells cultured on transwell filters, an established in vitro model of intestinal epithelium. Since micronutrient deficiency may accelerate mitochondrial efficiency, the mitochondrial response of these cells, in the presence of MnGluc and MnOxP, by microscopy methods and by ATP luminescence assay was used. Results In the presence of both MnOxP and MnGluc a sustained mitochondrial activity was shown by mitoTraker labeling (indicative of mitochondrial respiration, but ATP intracellular content remained comparable to untreated cells only in the presence of MnOxP. In addition MnOxP transiently up-regulated the antioxidant enzyme Mn superoxide dismutase more efficiently than MnGluc. Both metal treatments preserved NADH and βNADPH diaphorase oxidative activity, avoided mitochondrial dysfunction, as assessed by the absence of a sustained phosphoERK activation, and were able to maintain cell viability. Conclusions Collectively, our data indicate that MnOxP and MnGluc, and primarily the former, produce a moderate and safe modification of Caco-2 cell metabolism, by activating positive enzymatic mechanisms, thus could contribute to long-term maintenance of cell homeostasis.

  6. Synthesis, Structure, and Electrical Properties of the Mo12 Cluster Sulfide Hg∼2.8KMo12S14 Containing Mercury Chains.

    Science.gov (United States)

    Gougeon, Patrick; Gall, Philippe

    2017-03-20

    The new compound Hg∼2.8KMo12S14 was synthesized by diffusing mercury into the metastable KMo12S14 compound at 350 °C. Its crystallographic structure, solved from single-crystal X-ray diffraction, shows that the Mo-S framework is maintained during the synthesis. It is based on Mo12S14S6 units interlinked via Mo-S bonds as in the parent compound. The mercury forms linear chains with Hg-Hg distances of about 2.72 Å in the tunnels delimited by the Mo12S14S6 units. Superconductivity was observed below 2.5 K by electrical resistivity and magnetic susceptibility measurements.

  7. Microstructure and phase transformation behavior of Mo-MoSi2 gradient material

    Institute of Scientific and Technical Information of China (English)

    Ying-Yi Zhang; Yun-Gang Li; Yong-Hong Qi; Xue-Feng Shi

    2015-01-01

    Mo-MoSi2 gradient coating on Mo substrate was prepared by siliconizing process,using the polysilicon as silicon atoms.The gradient layer was analyzed by the experimental results,theoretical analysis,and thermodynamic calculation.The silicon,molybdenum content of gradient coating shows a gradual change regulation.The reaction between silicon and molybdenum is most likely to generate Mo5Si3,then MoSi2,finally Mo3Si,but when the silicon content is excessive,the Mo5Si3 and Mo3Si will react with silicon and generate MoSi2.The gradient layer is mainly constituted by Si and MoSi2,only about 1/10 gradient layer is constituted by Mo5Si3 and Mo3Si,and the stable existences of Mo5Si3 and Mo3Si are mainly determined by the silicon content.Along the Mo substrate to the surface of the coating,the phase compo sition of gradient coating changes as follows:Mo → transition layer,Mo (main phase) + Mo3Si + Mo5Si3 →intermediate layer,and MoSi2 (main phase)+ Mo5Si3 + Si → surface layer MoSi2 (main phase)+ Si,and the experimental temperature has no effect on phase composition of gradient coating.

  8. Search for the <mn>0mn>--> glueball in Υ<mo stretchy='false'>(mo>>1mn>S stretchy='false'>)mo> and Υ<mo stretchy='false'>(mo>>2mn>S stretchy='false'>)mo> decays

    Energy Technology Data Exchange (ETDEWEB)

    Jia, S.; Shen, C. P.; Yuan, C. Z.; Adachi, I.; Aihara, H.; Al Said, S.; Asner, D. M.; Aushev, T.; Ayad, R.; Babu, V.; Badhrees, I.; Bakich, A. M.; Bansal, V.; Barberio, E.; Behera, P.; Bhuyan, B.; Biswal, J.; Bonvicini, G.; Bozek, A.; Bračko, M.; Browder, T. E.; Červenkov, D.; Chang, P.; Chekelian, V.; Chen, A.; Cheon, B. G.; Chilikin, K.; Cho, K.; Choi, S. -K.; Choi, Y.; Cinabro, D.; Dash, N.; Di Carlo, S.; Doležal, Z.; Drásal, Z.; Dutta, D.; Eidelman, S.; Farhat, H.; Fast, J. E.; Ferber, T.; Fulsom, B. G.; Gaur, V.; Gabyshev, N.; Garmash, A.; Gillard, R.; Goldenzweig, P.; Golob, B.; Haba, J.; Hara, T.; Hayasaka, K.; Hayashii, H.; Hedges, M. T.; Hou, W. -S.; Iijima, T.; Inami, K.; Inguglia, G.; Ishikawa, A.; Itoh, R.; Jaegle, I.; Joffe, D.; Joo, K. K.; Julius, T.; Kang, K. H.; Katrenko, P.; Kawasaki, T.; Kichimi, H.; Kiesling, C.; Kim, D. Y.; Kim, H. J.; Kim, J. B.; Kim, K. T.; Kim, M. J.; Kim, S. H.; Kim, Y. J.; Kodyš, P.; Korpar, S.; Kotchetkov, D.; Križan, P.; Krokovny, P.; Kuhr, T.; Kulasiri, R.; Kuzmin, A.; Kwon, Y. -J.; Lange, J. S.; Li, C. H.; Li, L.; Li, Y.; Li Gioi, L.; Libby, J.; Liventsev, D.; Lubej, M.; Luo, T.; Masuda, M.; Matsuda, T.; Matvienko, D.; Miyabayashi, K.; Miyata, H.; Mizuk, R.; Moon, H. K.; Mori, T.; Nakao, M.; Nanut, T.; Nath, K. J.; Natkaniec, Z.; Nayak, M.; Niiyama, M.; Nisar, N. K.; Nishida, S.; Ogawa, S.; Okuno, S.; Ono, H.; Onuki, Y.; Ostrowicz, W.; Pakhlova, G.; Pal, B.; Park, C. -S.; Park, H.; Pestotnik, R.; Piilonen, L. E.; Pulvermacher, C.; Ritter, M.; Rostomyan, A.; Sakai, Y.; Sandilya, S.; Santelj, L.; Sanuki, T.; Savinov, V.; Schneider, O.; Schnell, G.; Schwanda, C.; Seino, Y.; Senyo, K.; Sevior, M. E.; Shebalin, V.; Shibata, T. -A.; Shiu, J. -G.; Shwartz, B.; Simon, F.; Sokolov, A.; Solovieva, E.; Starič, M.; Strube, J. F.; Sumihama, M.; Sumiyoshi, T.; Suzuki, K.; Takizawa, M.; Tamponi, U.; Tanida, K.; Tenchini, F.; Uchida, M.; Uglov, T.; Unno, Y.; Uno, S.; Urquijo, P.; Usov, Y.; Van Hulse, C.; Varner, G.; Vorobyev, V.; Wang, C. H.; Wang, M. -Z.; Wang, P.; Watanabe, Y.; Widmann, E.; Won, E.; Yamashita, Y.; Ye, H.; Yelton, J.; Zhang, Z. P.; Zhilich, V.; Zhukova, V.; Zhulanov, V.; Zupanc, A.

    2017-01-01

    We report the first search for the JPC= 0-- glueball in Yð1SÞ and Y=ð2SÞ decays with data samples of (102 ± 2) × 106 and (158 ± 4) × 106 events, respectively, collected with the Belle detector. No significant signals are observed in any of the proposed production modes, and the 90% credibility level upper limits on their branching fractions in Y(1S) andY(2S) decays are obtained. The inclusive branching fractions of the Y(1S) and Y(2S) decays into final states with a χc1 are measured to be B(Y(1S) → χc1 þ anything = (1.90± 0.43(stat) ± 0.14(syst)) × 10-4 with an improved precision over prior measurements and → χc1 + anything) = (2.24 ±0.44(stat) 0.20(syst)) × 10-4 for the first time.

  9. An investigation for the HgCdTe cleaning process

    Science.gov (United States)

    Lan, Tian-Yi; Wang, Nili; Zhao, Shuiping; Liu, Shi-Jia; Li, Xiang-Yang

    2014-11-01

    A new cleaning process for HgCdTe was designed - which used the improved SC-1,SC-2 and Br2- C2H5OH solutions as the main cleaning fluid and applied mega sound waves in the cleaning process. By analyzing the test results carried out on the HgCdTe surface, it was found that the material of HgCdTe for the application of new cleaning process was better than the one for the application of conventional cleaning process in the minority carrier lifetime, residual organic contamination, responsivity and specific detectivity.

  10. Doping and Diffusion in HgCdTe

    Science.gov (United States)

    1991-01-28

    In’i, -InT. Te - 1.8 ( - 3 .5 )h ( + 2.9 - 6/) TeT1’- Tej . 4 Hg rich HgCdTe Hg - 1.8 + 1.2 + 1.4 - 2p H - ’g, - H g j.. ’TI - tetrahedral position...A. Anderson, Appl. Phys. Lett. 53, 11.81 (1988). B. D. Patterson, Rev. Mod. Phys. 60, 69 (1988). 60 V. A. Singh , C. Weigel, J. W. Corbett, and L. M

  11. Estimating mercury emission outflow from East Asia using CMAQ-Hg

    Directory of Open Access Journals (Sweden)

    C.-J. Lin

    2009-10-01

    Full Text Available East Asia contributes nearly 50% of the global anthropogenic mercury emissions into the atmosphere. Recently, there are concerns for the long-range transport of mercury from East Asia to North America, which may lead to enhanced dry and wet depositions in North America. In this study, we performed four monthly simulations (January, April, July and October in 2005 using CMAQ-Hg v4.6 in an East Asian model domain. Coupled with a mass balance analysis and a number of emission inventory scenarios, the chemical transport of atmospheric mercury, the seasonal mercury transport budgets and mercury emission outflow from the East Asian region were investigated. The total annual mercury deposition in the region for the modeling year is estimated to be 821 Mg, with 396 Mg contributed by wet deposition and 425 Mg contributed by dry deposition. Regional mercury transport budgets show strong seasonal variability, with a net removal of RGM (7~5 Mg mo−1 and PHg (13~21 Mg mo−1, and a net export of GEM (60~130 Mg mo−1 from the study domain. The annual outflow caused by the East Asian emission is estimated to be in the range of 1369~1671 Mg yr−1, primarily in the form of GEM. This represents about 75% of the total mercury emissions (anthropogenic and natural in the region. The emission outflow from this source region would contribute to 20~30% of mercury deposition in areas remote from anthropogenic emission sources.

  12. Mott localization in a pure stripe antiferromagnet Rb<mn>1mn><mo>-mo>δFe<mn>1.5mn>->σS<mn>2mn>

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Meng; Yi, Ming; Cao, Huibo; de la Cruz, C.; Mo, S. K.; Huang, Q. Z.; Bourret-Courchesne, E.; Dai, Pengcheng; Lee, D. H.; Shen, Z. X.; Birgeneau, R. J.

    2015-09-01

    A combination of neutron diffraction and angle-resolved photoemission spectroscopy measurements on a pure antiferromagnetic stripe Rb1-δFe1.5-σS2 is reported. A neutron diffraction experiment on a powder sample shows that a 98% volume fraction of the sample is in the antiferromagnetic stripe phase with rhombic iron vacancy order and a refined composition of Rb0.66Fe1.36S2, and that only 2% of the sample is in the block antiferromagnetic phase with √5×√5 iron vacancy order. Furthermore, a neutron diffraction experiment on a single crystal shows that there is only a single phase with the stripe antiferromagnetic order with the refined composition of Rb0.78Fe1.35S2, while the phase with block antiferromagnetic order is absent. Angle-resolved photoemission spectroscopy measurements on the same crystal with the pure stripe phase reveal that the electronic structure is gapped at the Fermi level with a gap larger than 0.325 eV. The data collectively demonstrate that the extra 10% iron vacancies in addition to the rhombic iron vacancy order effectively impede the formation of the block antiferromagnetic phase; the data also suggest that the stripe antiferromagnetic phase with rhombic iron vacancy order is a Mott insulator.

  13. Hg, Bi, Cu and Zn distribution in human teeth treated by dental amalgam measured by synchrotron microprobe

    Science.gov (United States)

    Carvalho, M. L.; Marques, J. P.; Brito, J.; Casaca, C.; Cunha, A. S.

    2002-11-01

    Human teeth restored with dental amalgam were analysed by a synchrotron microprobe to evaluate the diffusion of its major constituents, Cu, Zn and Hg, throughout the tooth structures. We measured the elemental distribution inside the tooth from the root to the enamel, specially the region around the amalgam, after its total removal. Hg is present only in restored teeth and concentration profiles show strongly increased levels of this element close to the amalgam region, reaching 500 μg g -1 in one or two cases, decreasing strongly to the inner part of the tooth. Pb concentration profiles do not seem to be affected by metallic amalgam. Very high concentrations of Bi were found in one of the restored teeth, reaching more than 2000 μg g -1, decreasing sharply to the outer regions. The distribution of Mn, Fe, Cu and Zn was also determined in order to evaluate elemental influences by amalgam components. No significant changes in elemental concentrations were detected for Mn and Fe between healthy and restored teeth. However, the levels of Zn and Cu are increased in restored teeth. An X-ray fluorescence set-up with microprobe capabilities, 100 μm of spatial resolution and an energy of 18 keV, installed at LURE synchrotron (France) was used.

  14. Hg, Bi, Cu and Zn distribution in human teeth treated by dental amalgam measured by synchrotron microprobe

    Energy Technology Data Exchange (ETDEWEB)

    Carvalho, M.L. E-mail: luisa@cii.fc.ul.pt; Marques, J.P.; Brito, J.; Casaca, C.; Cunha, A.S

    2002-11-01

    Human teeth restored with dental amalgam were analysed by a synchrotron microprobe to evaluate the diffusion of its major constituents, Cu, Zn and Hg, throughout the tooth structures. We measured the elemental distribution inside the tooth from the root to the enamel, specially the region around the amalgam, after its total removal. Hg is present only in restored teeth and concentration profiles show strongly increased levels of this element close to the amalgam region, reaching 500 {mu}g g{sup -1} in one or two cases, decreasing strongly to the inner part of the tooth. Pb concentration profiles do not seem to be affected by metallic amalgam. Very high concentrations of Bi were found in one of the restored teeth, reaching more than 2000 {mu}g g{sup -1}, decreasing sharply to the outer regions. The distribution of Mn, Fe, Cu and Zn was also determined in order to evaluate elemental influences by amalgam components. No significant changes in elemental concentrations were detected for Mn and Fe between healthy and restored teeth. However, the levels of Zn and Cu are increased in restored teeth. An X-ray fluorescence set-up with microprobe capabilities, 100 {mu}m of spatial resolution and an energy of 18 keV, installed at LURE synchrotron (France) was used.

  15. Sedimentological control on Mn, and other trace elements, in groundwater of the Bengal delta.

    Science.gov (United States)

    McArthur, J M; Sikdar, P K; Nath, B; Grassineau, N; Marshall, J D; Banerjee, D M

    2012-01-17

    To reveal what controls the concentration and distribution of possibly hazardous (Mn, U, Se, Cd, Bi, Pb) and nonhazardous (Fe, V, Mo, PO(4)) trace elements in groundwater of the Bengal delta, we mapped their concentrations in shallow groundwater (sedimentology and sources of water. Areas of less negative δ(18)O reveal recharge by sources of evaporated water. Concentrations of Fe, As, Mo, and PO(4) are high in palaeo-channel groundwaters and low in palaeo-interfluvial groundwaters. Concentrations of U, V, and Mn, are low in palaeo-channel groundwaters and high in palaeo-interfluvial groundwaters. Concentrations of Fe and Mn are highest (18 and 6 mg/L respectively) at dual reduction-fronts that form strip interfaces at depth around the edges of palaeo-interfluvial aquifers. The fronts form as focused recharge carries dissolved organic carbon into the aquifer margins, which comprise brown, iron-oxide bearing, sand. At the Mn-reduction front, concentrations of V and Mo reach peak concentrations of 3 μg/L. At the Fe-reduction front, concentrations of PO(4) and As reach concentrations 3 mg/L and 150 μg/L respectively. Many groundwaters contain >10 mg/L of Cl, showing that they are contaminated by Cl of anthropogenic origin and that organic matter from in situ sanitation may contribute to driving reduction.

  16. Uptake of HgCl{sub 2} and MeHgCl in an insect cell line (Aedes albopictus C6/36)

    Energy Technology Data Exchange (ETDEWEB)

    Braeckman, B.; Cornelis, R.; Rzeznik, U.; Raes, H. [Univ. of Ghent (Belgium)

    1998-10-01

    The authors studied the uptake mechanism of mercuric chloride (Hg) and methylmercuric chloride (MeHg) in Aedes albopictus C6/36 cells. The uptake kinetics, together with the effect of temperature and a metabolic inhibitor (2,4-dinitrophenol) on the mercury accumulation, were examined. Both amounts of internalized Hg and MeHg increased linearly with the extracellular concentration. Initially, the influx rate was high for both metal species but MeHg was found to accumulate seven times faster than Hg. At longer exposure times it leveled off for Hg, while for MeHg, the intracellular concentration decreased. Hg toxicity was not significantly influenced by elevated temperatures; in contrast there was a marked decrease of the LC{sub 50/24 h} value for MeHg. On the other hand, Hg accumulation was temperature dependent but MeHg was not. The different toxicity and uptake rate of both mercury compounds can be explained in terms of membrane permeability and target site. For Hg the main target seems to be the plasma membrane, while MeHg readily crosses this barrier and reacts with intracellular targets. 2,4-Dinitrophenol had no effect on the accumulation of Hg but that of MeHg was doubled.

  17. Results Of Hg Speciation Testing On DWPF SMECT-1, SMECT-3, And SMECT-5 Samples

    Energy Technology Data Exchange (ETDEWEB)

    Bannochie, C. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2016-01-07

    The Savannah River National Laboratory (SRNL) was tasked with preparing and shipping samples for Hg speciation by Eurofins Frontier Global Sciences, Inc. in Seattle, WA on behalf of the Savannah River Remediation (SRR) Mercury Task Team. The thirteenth shipment of samples was designated to include Defense Waste Processing Facility (DWPF) Slurry Mix Evaporator Condensate Tank (SMECT) from Sludge Receipt and Adjustment Tank (SRAT) Batch 736 and 738 samples. Triplicate samples of each material were prepared for this shipment. Each replicate was analyzed for seven Hg species: total Hg, total soluble (dissolved) Hg, elemental Hg [Hg(0)], ionic (inorganic) Hg [Hg(I) and Hg(II)], methyl Hg [CH3Hg-X, where X is a counter anion], ethyl Hg [CH3CH2-Hg-X, where X is a counter anion], and dimethyl Hg [(CH3)2Hg]. The difference between the total Hg and total soluble Hg measurements gives the particulate Hg concentration, i.e. Hg adsorbed to the surface of particulate matter in the sample but without resolution of the specific adsorbed species. The average concentrations of Hg species in the aqueous samples derived from Eurofins reported data corrected for dilutions performed by SRNL are tabulated.

  18. Quantum Calorimeters Based on HgCdTe Alloys Project

    Data.gov (United States)

    National Aeronautics and Space Administration — NASA's next generation of x-ray observation missions require x-ray calorimeters with superior energy resolution. Semimetallic HgTe has already proven itself as an...

  19. Enrichment of Pb, Hg and Cr in cultured carp otolith

    African Journals Online (AJOL)

    AJL

    2012-01-26

    Jan 26, 2012 ... record the pollution condition at the sampling time. ... aquatic organisms are aquatic algae, zooplankton .... element cannot show that Hg concentration in otolith ..... from Atlantic croaker along an estuarine pollution gradient.

  20. Quantum Calorimeters Based on HgCdTe Alloys Project

    Data.gov (United States)

    National Aeronautics and Space Administration — NASA's next generation of x-ray observation missions require x-ray calorimeters with superior energy resolution. Semimetallic HgTe has already proven itself as an...

  1. Properties of Light Hg, Pb and Po Isotopes

    CERN Document Server

    Muntian, I

    2003-01-01

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

  2. Interaction of Hg Atom with Bare Si(111) Surface

    Institute of Scientific and Technical Information of China (English)

    LIU Yong-Jun; LIU Ying

    2006-01-01

    To evaluate the interaction between Hg atom and bare Si(111) surface, three types of silicon cluster models of Si4H7, Si7H10 and Si16H20 together with their Hg complexes were studied by using hybrid (U)B3LYP density functional theory method. Optimized geometries and energies for Hg atom on different adsorption sites indicate that: 1) the binding energies at different adsorption sites are small (ranging from ~3 to 8 kJ/mol dependent on the adsorption sites), suggesting a weak interaction between Hg atom and silicon surface; 2) the most favorable adsorption site is the on top (T) site. By analyzing their natural bonding orbitals, the possible reason of this difference is suggested.

  3. Spongelike Nanosized Mn 3 O 4 as a High-Capacity Anode Material for Rechargeable Lithium Batteries

    KAUST Repository

    Gao, Jie

    2011-07-12

    Mn3O4 has been investigated as a high-capacity anode material for rechargeable lithium ion batteries. Spongelike nanosized Mn 3O4 was synthesized by a simple precipitation method and characterized by powder X-ray diffraction, Raman scattering and scanning electron microscopy. Its electrochemical performance, as an anode material, was evaluated by galvanostatic discharge-charge tests. The results indicate that this novel type of nanosized Mn3O4 exhibits a high initial reversible capacity (869 mA h/g) and significantly enhanced first Coulomb efficiency with a stabilized reversible capacity of around 800 mA h/g after over 40 charge/discharge cycles. © 2011 American Chemical Society.

  4. A Mn-54 Radiotracer Study of Mn Isotope Solid-Liquid Exchange during Reductive Transformation of Vernadite (δ-MnO₂) by Aqueous Mn(II)

    Energy Technology Data Exchange (ETDEWEB)

    Elzinga, Evert J.; Kustka, Adam B. [Rutgers

    2015-04-09

    We employed Mn-54 radiotracers to characterize the extent and dynamics of Mn atom exchange between aqueous Mn(II) and vernadite (δ-Mn(IV)O2) at pH 7.5 under anoxic conditions. Exchange of Mn atoms between the solid and liquid phase is rapid, reaching dynamic equilibrium in 2–4 days. We propose that during the initial stages of reaction, Mn atom exchange occurs through consecutive comproportionation-disproportionation reactions where interfacial electron transfer from adsorbed Mn(II) to lattice Mn(IV) generates labile Mn(III) cations that rapidly disproportionate to reform aqueous Mn(II) and solid-phase Mn(IV). Following nucleation of Mn(III)OOH phases, additional exchange likely occurs through electron transfer from aqueous Mn(II) to solid-phase Mn(III). Our results provide evidence for the fast and extensive production of transient Mn(III) species at the vernadite surface upon contact of this substrate with dissolved Mn(II). We further show that HEPES buffer is a reductant of lattice Mn(IV) in the vernadite structure in our experiments. The methods and results presented here introduce application of Mn-54 tracers as a facile tool to further investigate the formation kinetics of labile Mn(III) surface species and their impacts on Mn-oxide structure and reactivity over a range of environmentally relevant geochemical conditions.

  5. Mo/MCM-41-Type mesoporous materials doubly promoted with Fe and Ni for hydrotreating reactions

    Energy Technology Data Exchange (ETDEWEB)

    Carlos F. Linares; Patricia Amezqueta; Carlos Scott [Universidad de Carabobo, Carabobo (Venezuela). Laboratorio de Catalisis y Metales de Transicion

    2008-09-15

    A Si-MCM-41-type material was synthesized and impregnated with a Mo solution in order to get a 15% MoO{sub 3} by weight. Then, it was doubly promoted with Ni and Fe in different proportions. Information on the structure of the precursors was revealed by XRD, TPR and surface area techniques. XRD results showed that the mesoporous materials were not affected for the successive impregnations carried out; while, their specific surface areas was partially blocked. These solids were tested for vanadyl octaethyl porphyrin hydrodeporphirinization (HDP), and individual and competitive reactions of dibenzothiophene (DBT) hydrodesulfurization (HDS) and 2-methyl naphthalene (2MN) hydrogenation (HYD). The DBT HDS activity was higher than 2MN HYD, and the presence of Fe in the catalysts did not produce a synergetic effect for this reactions. However, HDP activities of doubly promoted catalysts were superior to the monopromoted ones. 28 refs., 8 figs., 5 tabs.

  6. Cardiac dysfunction in HgCl2-induced nephrotic syndrome.

    Science.gov (United States)

    Moreira-Rodrigues, Mónica; Henriques-Coelho, Tiago; Moura, Cláudia; Vasques-Nóvoa, Francisco; Sampaio-Maia, Benedita; Pestana, Manuel; Leite-Moreira, Adelino F

    2010-03-01

    The experimental model of HgCl(2) injection is characterized by a systemic autoimmune disease which leads to the development of nephrotic syndrome (NS). NS seems to be accompanied by cardiovascular alterations, since patients with NS present an increased incidence in cardiac disease. The aim of our work was to study the effects of HgCl(2)-induced NS on myocardial function and morphometry. Normotensive Brown-Norway rats were injected with HgCl(2) (1 mg/kg, HgCl(2) group; n = 6, subcutaneous) or the vehicle (control group; n = 6, subcutaneous) on days 0, 2, 4, 7, 9 and 11. The animals were placed in metabolic cages for evaluation of urinary excretion of noradrenaline, sodium, total proteins, albumin and creatinine. Fourteen and 21 days after the first HgCl(2) injection, left ventricle (LV) hemodynamics was evaluated through pressure micromanometers in basal and isovolumetric heartbeats. The heart and gastrocnemius muscle weights and tibial length were also examined. In an additional group of animals cardiac dimensions and ejection fraction were assessed by echocardiography and LV apoptosis and fibrosis were studied. HgCl(2)-injected rats presented proteinuria, albuminuria, hyperlipidemia, anemia, sodium retention and ascites at day 14. These alterations were accompanied by LV hemodynamic changes only in isovolumetric heartbeats. Similarly, on day 21, HgCl(2)-injected rats presented proteinuria, albuminuria, hyperlipidemia, anemia, but no sodium retention or ascites. These animals presented LV systolic and diastolic dysfunction in both basal and isovolumetric heartbeats, as well as cardiac atrophy, LV fibrosis and an increase in myocyte apoptosis. In conclusion, HgCl(2)-induced NS is accompanied by LV dysfunction and can be a promising model for studying the link between NS and cardiac disease.

  7. First observation of excited states in 173Hg93

    CERN Document Server

    O'Donnell, D; Scholey, C; Bianco, L; Capponi, L; Carroll, R J; Darby, I G; Donosa, L; Drummond, M; Ertugral, F; Greenlees, P T; Grahn, T; Hauschild, K; Herzan, A; Jakobsson, U; Jones, P; Joss, D T; Julin, R; Juutinen, S; Ketelhut, S; Labiche, M; Leino, M; Lopez-Martens, A; Mullholland, K; Nieminen, P; Peura, P; Rahkila, P; Rinta-Antila, S; Ruotsalainen, P; Sandzelius, M; Saren, J; Saygi, B; Simpson, J; Sorri, J; Thornthwaite, A; Uusitalo, J

    2012-01-01

    The neutron-deficient nucleus 173Hg has been studied following fusion-evaporation reactions. The observation of gamma rays decaying from excited states are reported for the first time and a tentative level scheme is proposed. The proposed level scheme is discussed within the context of the systematics of neighbouring neutron-deficient Hg nuclei. In addition to the gamma-ray spectroscopy, the alpha decay of this nucleus has been measured yielding superior precision to earlier measurements.

  8. Fe-Mn bi-metallic oxides loaded on granular activated carbon to enhance dye removal by catalytic ozonation.

    Science.gov (United States)

    Tang, Shoufeng; Yuan, Deling; Zhang, Qi; Liu, Yameng; Zhang, Qi; Liu, Zhengquan; Huang, Haiming

    2016-09-01

    A Fe-Mn bi-metallic oxide supported on granular activated carbon (Fe-Mn GAC) has been fabricated by an impregnation-desiccation method and tested in the catalytic ozonation of methyl orange (MO) degradation and mineralization. X-ray diffraction, scanning electron microscopy, and Fourier transform infrared spectroscopy characterizations revealed that Fe-Mn oxides were successfully loaded and uniformly distributed on the GAC, and nitrogen adsorption isotherms showed that the supported GAC retained a large surface area and a high pore volume compared with the pristine GAC. The catalytic activity was systematically assessed by monitoring the MO removal efficiencies at different operational parameters, such as catalyst dosage, initial solution pH, and ozone flow rate. The Fe-Mn GAC exhibited better catalytic activity relative to ozone alone and GAC alone, improving the TOC removal by 24.5 and 11.5 % and COD removal by 13.6 and 7.3 %, respectively. The reusability of the hybrid was examined over five consecutive cyclic treatments. The Fe-Mn GAC catalytic activity was only a slight loss in the cycles, showing good stability. The addition of Na2CO3 as hydroxyl radicals (•OH) scavengers proved that the catalytic ozonation mechanism was the enhanced generation of •OH by the Fe-Mn GAC. The above results render the Fe-Mn GAC an industrially promising candidate for catalytic ozonation of dye contaminant removal.

  9. Synthesis of Mn-sensitized TiO{sub 2}nanoparticles: influence of sequence of reagents on phase composition and photocatalytic activity

    Energy Technology Data Exchange (ETDEWEB)

    Kuzmicheva, Galina M.; Savinkina, Elena V., E-mail: e.savinkina@mail.ru; Obolenskaya, Lubov N. [Lomonosov University of Fine Chemical Technology (Russian Federation); Zubavichus, Yan V.; Murzin, Vadim Y. [National Research Center “Kurchatov Institute” (Russian Federation); Podbelskiy, Vadim V. [National Research University Higher School of Economics (Russian Federation); Sadovskaya, Nataliya V. [Karpov Institute of Physical Chemistry (Russian Federation)

    2015-10-15

    A new approach has been developed to synthesize manganese-containing titanium dioxide materials by hydrolysis of titanyl sulfate. The samples were studied by a complex of methods (synchrotron radiation X-ray powder diffraction, high-resolution scanning electron microscopy with energy-dispersive X-ray spectroscopy, absorption spectroscopy). The sequence of the added reagents effects the phase composition (anatase or mixtures of anatase and “η-TiO{sub 2}”), size of crystallites, nanoparticles and agglomerates, manganese content, and oxidation state (Mn{sup 3+}, Mn{sup 2+}/Mn{sup 3+}, or Mn{sup 3+}/Mn{sup 4+}). The Mn-doped TiO{sub 2} samples have been proven to have high photocatalytic activity for methyl orange (MO) under visible light. The rate of MO degradation reached 0.0046 min{sup −1} (50 % in 150 min) for the sample containing a mixture of anatase (75 %) and “η-TiO{sub 2}” (25 %) with a high degree of amorphism; the sample is characterized by the smallest size of crystallites (44.3 Å), the largest size of nanoparticles (33 nm) and agglomerates (10 μm), and the lowest manganese content (0.3 at. %) with the ratio Mn{sup 3+}:Mn{sup 4+} = 1:1. The resultant Mn-doped titania has potential applications in photocatalysis and environmental protection.

  10. Crystal structure of K[Hg(SCN)3] - a redetermination.

    Science.gov (United States)

    Weil, Matthias; Häusler, Thomas

    2014-09-01

    The crystal structure of the room-temperature modification of K[Hg(SCN)3], potassium tri-thio-cyanato-mercurate(II), was redetermined based on modern CCD data. In comparison with the previous report [Zhdanov & Sanadze (1952 ▶). Zh. Fiz. Khim. 26, 469-478], reliability factors, standard deviations of lattice parameters and atomic coordinates, as well as anisotropic displacement parameters, were revealed for all atoms. The higher precision and accuracy of the model is, for example, reflected by the Hg-S bond lengths of 2.3954 (11), 2.4481 (8) and 2.7653 (6) Å in comparison with values of 2.24, 2.43 and 2.77 Å. All atoms in the crystal structure are located on mirror planes. The Hg(2+) cation is surrounded by four S atoms in a seesaw shape [S-Hg-S angles range from 94.65 (2) to 154.06 (3)°]. The HgS4 polyhedra share a common S atom, building up chains extending parallel to [010]. All S atoms of the resulting (1) ∞[HgS2/1S2/2] chains are also part of SCN(-) anions that link these chains with the K(+) cations into a three-dimensional network. The K-N bond lengths of the distorted KN7 polyhedra lie between 2.926 (2) and 3.051 (3) Å.

  11. Self-powered sensor for trace Hg2+ detection.

    Science.gov (United States)

    Wen, Dan; Deng, Liu; Guo, Shaojun; Dong, Shaojun

    2011-05-15

    A self-powered electrochemical sensor has been facilely designed for sensitive detection of Hg(2+) based on the inhibition of biocatalysis process of enzymatic biofuel cell (BFC) for the first time. The as-prepared one-compartment BFC, which was consisted of alcohol dehydrogenase supported on single-walled carbon nanohorns-based mediator system as the anode and bilirubin oxidase as the cathodic biocatalyst, generated an open circuit potential (V(oc)) of 636 mV and a maximum power density of 137 μW cm(-2). It was interestingly found that the presence of Hg(2+) would affect the performance of the constructed BFC (e.g., V(oc)). Taking advantage of the inhibitive effect of Hg(2+), a novel self-powered Hg(2+) sensor has been developed, which showed a linear range of 1-500 nM (R(2) = 0.999) with a detection limit of 1 nM at room temperature. In addition, this BFC-type sensor exhibited good selectivity for Hg(2+) against other common environmental metal ions, and the feasibility of the method for Hg(2+) detection in actual water samples (i.e., tap, ground, and lake water) was demonstrated with satisfactory results.

  12. Transcriptional and phenotypic changes in aorta and aortic valve with aging and MnSOD deficiency in mice.

    Science.gov (United States)

    Roos, Carolyn M; Hagler, Michael; Zhang, Bin; Oehler, Elise A; Arghami, Arman; Miller, Jordan D

    2013-11-15

    The purpose of this study was to characterize changes in antioxidant and age-related gene expression in aorta and aortic valve with aging, and test the hypothesis that increased mitochondrial oxidative stress accelerates age-related endothelial and aortic valve dysfunction. Wild-type (MnSOD(+/+)) and manganese SOD heterozygous haploinsufficient (MnSOD(+/-)) mice were studied at 3 and 18 mo of age. In aorta from wild-type mice, antioxidant expression was preserved, although there were age-associated increases in Nox2 expression. Haploinsufficiency of MnSOD did not alter antioxidant expression in aorta, but increased expression of Nox2. When compared with that of aorta, age-associated reductions in antioxidant expression were larger in aortic valves from wild-type and MnSOD haploinsufficient mice, although Nox2 expression was unchanged. Similarly, sirtuin expression was relatively well-preserved in aorta from both genotypes, whereas expression of SIRT1, SIRT2, SIRT3, SIRT4, and SIRT6 were significantly reduced in the aortic valve. Expression of p16(ink4a), a marker of cellular senescence, was profoundly increased in both aorta and aortic valve from MnSOD(+/+) and MnSOD(+/-) mice. Functionally, we observed comparable age-associated reductions in endothelial function in aorta from both MnSOD(+/+) and MnSOD(+/-) mice. Interestingly, inhibition of NAD(P)H oxidase with apocynin or gp91ds-tat improved endothelial function in MnSOD(+/+) mice but significantly impaired endothelial function in MnSOD(+/-) mice at both ages. Aortic valve function was not impaired by aging or MnSOD haploinsufficiency. Changes in antioxidant and sirtuin gene expression with aging differ dramatically between aorta and aortic valve. Furthermore, although MnSOD does not result in overt cardiovascular dysfunction with aging, compensatory transcriptional responses to MnSOD deficiency appear to be tissue specific.

  13. Real-time selective visual monitoring of Hg(2+) detection at ppt level: An approach to lighting electrospun nanofibers using gold nanoclusters.

    Science.gov (United States)

    Senthamizhan, Anitha; Celebioglu, Asli; Uyar, Tamer

    2015-05-28

    In this work, fluorescent gold nanocluster (AuNC) decorated polycaprolactone (PCL) nanofibers (AuNC*PCL-NF) for real time visual monitoring of Hg(2+) detection at ppt level in water is demonstrated. The resultant AuNC*PCL-NF exhibiting remarkable stability more than four months at ambient environment and facilitates increased accessibility to active sites resulting in improved sensing performance with rapid response time. The fluorescence changes of AuNC*PCL-NF and their corresponding time dependent spectra, upon introduction of Hg(2+), led to the visual identification of the sensor performance. It is observed that the effective removal of excess ligand (bovine serum albumin (BSA) greatly enhances the surface exposure of AuNC and therefore their selective sensing performance is achieved over competent metal ions such as Cu(2+), Ni(2+), Mn(2+), Zn(2+), Cd(2+), and Pb(2+) present in the water. An exceptional interaction is observed between AuNC and Hg(2+), wherein the absence of excess interrupting ligand makes AuNC more selective towards Hg(2+). The underlying mechanism is found to be due to the formation of Au-Hg amalgam, which was further investigated with XPS, TEM and elemental mapping studies. In short, our findings may lead to develop very efficient fluorescent-based nanofibrous mercury sensor, keeping in view of its stability, simplicity, reproducibility, and low cost.

  14. Real-time selective visual monitoring of Hg2+ detection at ppt level: An approach to lighting electrospun nanofibers using gold nanoclusters

    Science.gov (United States)

    Senthamizhan, Anitha; Celebioglu, Asli; Uyar, Tamer

    2015-05-01

    In this work, fluorescent gold nanocluster (AuNC) decorated polycaprolactone (PCL) nanofibers (AuNC*PCL-NF) for real time visual monitoring of Hg2+ detection at ppt level in water is demonstrated. The resultant AuNC*PCL-NF exhibiting remarkable stability more than four months at ambient environment and facilitates increased accessibility to active sites resulting in improved sensing performance with rapid response time. The fluorescence changes of AuNC*PCL-NF and their corresponding time dependent spectra, upon introduction of Hg2+, led to the visual identification of the sensor performance. It is observed that the effective removal of excess ligand (bovine serum albumin (BSA) greatly enhances the surface exposure of AuNC and therefore their selective sensing performance is achieved over competent metal ions such as Cu2+, Ni2+, Mn2+, Zn2+, Cd2+, and Pb2+ present in the water. An exceptional interaction is observed between AuNC and Hg2+, wherein the absence of excess interrupting ligand makes AuNC more selective towards Hg2+. The underlying mechanism is found to be due to the formation of Au-Hg amalgam, which was further investigated with XPS, TEM and elemental mapping studies. In short, our findings may lead to develop very efficient fluorescent-based nanofibrous mercury sensor, keeping in view of its stability, simplicity, reproducibility, and low cost.

  15. Persistent Hg contamination and occurrence of Hg-methylating transcript (hgcA) downstream of a chlor-alkali plant in the Olt River (Romania).

    Science.gov (United States)

    Bravo, Andrea G; Loizeau, Jean-Luc; Dranguet, Perrine; Makri, Stamatina; Björn, Erik; Ungureanu, Viorel Gh; Slaveykova, Vera I; Cosio, Claudia

    2016-06-01

    Chlor-alkali plants using mercury (Hg) cell technology are acute point sources of Hg pollution in the aquatic environment. While there have been recent efforts to reduce the use of Hg cells, some of the emitted Hg can be transformed to neurotoxic methylmercury (MeHg). Here, we aimed (i) to study the dispersion of Hg in four reservoirs located downstream of a chlor-alkali plant along the Olt River (Romania) and (ii) to track the activity of bacterial functional genes involved in Hg methylation. Total Hg (THg) concentrations in water and sediments decreased successively from the initial reservoir to downstream reservoirs. Suspended fine size particles and seston appeared to be responsible for the transport of THg into downstream reservoirs, while macrophytes reflected the local bioavailability of Hg. The concentration and proportion of MeHg were correlated with THg, but were not correlated with bacterial activity in sediments, while the abundance of hgcA transcript correlated with organic matter and Cl(-) concentration, indicating the importance of Hg bioavailability in sediments for Hg methylation. Our data clearly highlights the importance of considering Hg contamination as a legacy pollutant since there is a high risk of continued Hg accumulation in food webs long after Hg-cell phase out.

  16. Magnetic Properties of Orthorhornbic Perovskite Ho1-χLaχMnO3

    Institute of Scientific and Technical Information of China (English)

    WANG Hong-Tao; ZHOU Tong; HONG Bo; TAO Qian; XU Zhu-An

    2011-01-01

    Single phase orthorhombic perovskite Ho1-xLaxMnO3 (x = 0.1,0.15) compounds are successfully synthesized by using a sol-gel method. We find that the orthorhombic perovskite structure of HoMoO3 compound can be stabilized by partial substitution of smaller Ho ion by larger La ion. The magnetic properties of orthorhombic perovskite Ho1-xLaxMnO3 are investigated for the first time. For the x = 0.15 sample, a ferromagnetic-like transition is found around T = 130 K, which should correspond to partial FM ordering of Mn3+ magnetic moments. The partial substitution of Ho by La causes a switch of magnetic state of Mn3+ moments from AFM order to FM-like order. Our study indicates that La doping has significant influence on the magnetic structures of Mn ions.%@@ Single phase orthorhombic perovskite Ho1-xLaxMn03 (x = 0.1,0.15) compounds are successfully synthesized by using a sol-gel method.We find that the orthorhombic perovskite structure of H0M0O3 compound can be stabilized by partial substitution of smaller Ho ion by larger La ion.The magnetic properties of orthorhombic perovskite Ho1-xLaxMnO3 are investigated for the first time.For the x = 0.15 sample, a ferromagnetic-like transition is found around T = 130 K, which should correspond to partial FM ordering of Mn3+ magnetic moments.The partial substitution of Ho by La causes a switch of magnetic state of Mn3+ moments from AFM order to FM-like order.Our study indicates that La doping has significant influence on the magnetic structures of Mn ions.

  17. Hg $L_{3}$ edge absorption study of the $HgBa_{2}CuO_{4}\\delta$ superconductor

    CERN Document Server

    Ziyu, Wu; Bianconi, A

    2001-01-01

    The HgBa/sub 2/CuO/sub 4+ delta / superconductor has been studied by high resolution Hg L/sub 3/ X-ray absorption near-edge structure (XANES) spectroscopy. The XANES spectrum has been simulated by full multiple-scattering calculations in order to explore the origin of different features in the experimental spectrum. The experimental Hg L/sub 3/-edge spectrum could be well reproduced by considering a cluster of 85 atoms, containing 10 shells, within a radius of about 7 AA from the central Hg atom. The low energy spectral feature in the XANES spectrum is found to be due to a transition from the Hg p states to the electronic states hybridized with higher shell Ba atoms. This implies that the transition features in the Hg L/sub 3/- edge XANES are strongly influenced by medium range order effects unlike the case of L/sub 3/ edge of 3d transition metals where short- range order is enough to describe the main transition features. (25 refs).

  18. Hg SOIL GAS AND Hg SOIL DISTRIBUTION AROUND FORMER „ZRINSKI“ MINE ON MT. MEDVEDNICA, CROATIA

    Directory of Open Access Journals (Sweden)

    Nataša Jug

    2008-12-01

    Full Text Available The purpose of this study is to present the field and laboratory researches, statistical analyses and graphical displays of the results of Hg soil gas and Hg soil distribution in the area around former mining site „Zrinski“ on Mt. Medvednica. The values of overall Hg concentrations in the soil gas show lognormal distribution, and their spatial distribution outlines the connection with the present Pb-Ag-Zn mineralization and confirms anthropogenic origin of uneven landscape relief (waste rock clusters. Regression analysis of the dependence between Hg contents in the soil gas and the distance from the mine entrance (correlation coefficient r also points to the considerable spatial dependence. Hg soil contents show as well distribution similar to lognormal, and there is a slight correlation when compared with Hg soil gas content. Concentrations are mostly within background values, except in the immediate vicinity of the mine entrance where the values are significantly higher due to the mineralization influence concentrated in the waste-rock clusters. Soil pollution caused by mercury is of local character with the spreading tendency to the south-west because of the dominant relief influence. Mercury found in the soil of the research location derives from the present mineral body and former mining activities, while possible anthropogenic atmospheric inputs from remote sources can not be proven on the basic of conducted research studies (the paper is published in Croatian.

  19. Magnetic MoS2 pizzas and sandwiches with Mnn (n = 1–4) cluster toppings and fillings: A first-principles investigation

    Science.gov (United States)

    Zhang, Meng; Huang, Zhongjia; Wang, Xiao; Zhang, Hongyu; Li, Taohai; Wu, Zhaolong; Luo, Youhua; Cao, Wei

    2016-01-01

    The inorganic layered crystal (ILC) MoS2 in low dimensions is considered as one of the most promising and efficient semiconductors. To enable the magnetism and keep intrinsic crystal structures, we carried out a first-principles study of the magnetic and semiconductive monolayer MoS2 adsorbed with the Mnn (n = 1–4) clusters, and bilayer MoS2 intercalated with the same clusters. Geometric optimizations of the Mnn@MoS2 systems show the complexes prefer to have Mnn@MoS2(M) pizza and Mnn@MoS2(B) sandwich forms in the mono- and bi-layered cases, respectively. Introductions of the clusters will enhance complex stabilities, while bonds and charge transfers are found between external Mn clusters and the S atoms in the hosts. The pizzas have medium magnetic moments of 3, 6, 9, 4 μB and sandwiches of 3, 2, 3, 2 μB following the manganese numbers. The pizzas and sandwiches are semiconductors, but with narrower bandgaps compared to their corresponding pristine hosts. Direct bandgaps were found in the Mnn@MoS2(M) (n = 1,4) pizzas, and excitingly in the Mn1@MoS2(B) sandwich. Combining functional clusters to the layered hosts, the present work shows a novel material manipulation strategy to boost semiconductive ILCs applications in magnetics.

  20. Magnetic MoS2 pizzas and sandwiches with Mnn (n = 1-4) cluster toppings and fillings: A first-principles investigation.

    Science.gov (United States)

    Zhang, Meng; Huang, Zhongjia; Wang, Xiao; Zhang, Hongyu; Li, Taohai; Wu, Zhaolong; Luo, Youhua; Cao, Wei

    2016-01-01

    The inorganic layered crystal (ILC) MoS2 in low dimensions is considered as one of the most promising and efficient semiconductors. To enable the magnetism and keep intrinsic crystal structures, we carried out a first-principles study of the magnetic and semiconductive monolayer MoS2 adsorbed with the Mnn (n = 1-4) clusters, and bilayer MoS2 intercalated with the same clusters. Geometric optimizations of the Mnn@MoS2 systems show the complexes prefer to have Mnn@MoS2(M) pizza and Mnn@MoS2(B) sandwich forms in the mono- and bi-layered cases, respectively. Introductions of the clusters will enhance complex stabilities, while bonds and charge transfers are found between external Mn clusters and the S atoms in the hosts. The pizzas have medium magnetic moments of 3, 6, 9, 4 μB and sandwiches of 3, 2, 3, 2 μB following the manganese numbers. The pizzas and sandwiches are semiconductors, but with narrower bandgaps compared to their corresponding pristine hosts. Direct bandgaps were found in the Mnn@MoS2(M) (n = 1,4) pizzas, and excitingly in the Mn1@MoS2(B) sandwich. Combining functional clusters to the layered hosts, the present work shows a novel material manipulation strategy to boost semiconductive ILCs applications in magnetics.

  1. Superconducting Hg-Based Mixed Oxides and Oxyfluorides

    Science.gov (United States)

    Antipov, E. V.

    2000-09-01

    Syntheses under high pressure and under controlled mercury and oxygen partial pressures of different members of the HgBa2Can-1CunO2n+2+δ series have been developed. There are two main parameters influencing Tc in this family: width of a perovskite slab (n) and concentration (δ) of the extra oxygen located in the Hg layer. The increase of Tc with n occurs until the third member, while after that it decreases. All the members of the series exhibit similar cupola shaped dependencies of Tc vs. δ. Strongly overdoped high members of the series with n = 3-5 were prepared only using high pressure technique and BaO2 as an internal oxidizer. Neutron powder diffraction experiments were carried out for monophase oxygenated HgBa2CuO4F4+δ and fluorinated HgBa2CuO4Fδ samples with different extra oxygen or fluorine content and Tc values. Fluorinated series also exhibits the cupola -like behavior for the Tc vs. δ dependence. NPD showed twice the amount of extra fluorine in comparison with those for the oxygenated Hg-1201 phases with close Tc's. The exchange of the extra oxygen by double amount of fluorine causes shortening of the apical Cu-O distances, while the in-plane ones, as well as Tc, do not vary. The influence of the external pressure on the structure and Tc of Hg-1201 strongly depends on the doping level. The increase of the extra oxygen content on going from underdoped to overdoped state results in the larger compression of the apical Cu-O and Ba-OHg distances while the HgO2 dumbbell as well as the distance between Ba and O from the (CuO2) layers becomes practically pressure independent. These results together with the data for fluorinated materials allow to elucidate the crucial structural features responsible for the Tc variation under high pressure.

  2. Unexpected strong magnetism of Cu doped single-layer MoS₂ and its origin.

    Science.gov (United States)

    Yun, Won Seok; Lee, J D

    2014-05-21

    The magnetism of the 3d transition-metal (TM) doped single-layer (1L) MoS2, where the Mo atom is partially replaced by the 3d TM atom, is investigated using the first-principles density functional calculations. In a series of 3d TM doped 1L-MoS2's, the induced spin polarizations are negligible for Sc, Ti, and Cr dopings, while the induced spin polarizations are confirmed for V, Mn, Fe, Co, Ni, Cu, and Zn dopings and the systems become magnetic. Especially, the Cu doped system shows unexpectedly strong magnetism although Cu is nonmagnetic in its bulk state. The driving force is found to be a strong hybridization between Cu 3d states and 3p states of neighboring S, which results in an extreme unbalanced spin-population in the spin-split impurity bands near the Fermi level. Finally, we also discuss further issues of the Cu induced magnetism of 1L-MoS2 such as investigation of additional charge states, the Cu doping at the S site instead of the Mo site, and the Cu adatom on the layer (i.e., 1L-MoS2).

  3. Chern insulators without band inversion in Mo S2 monolayers with 3 d adatoms

    Science.gov (United States)

    Wei, Xinyuan; Zhao, Bao; Zhang, Jiayong; Xue, Yang; Li, Yun; Yang, Zhongqin

    2017-02-01

    Electronic and topological properties of Mo S2 monolayers endowed with 3 d transition metal (TM) adatoms (V-Fe) are explored by using ab initio methods and k .p models. Without the consideration of the Hubbard U interaction, the V, Cr, and Fe adatoms tend to locate on the top of the Mo atoms, while the most stable site for the Mn atom is at the hollow position of the Mo-S hexagon. After the Hubbard U is applied, the most stable sites of all the systems become the top of the Mo atoms. Chern insulators without band inversion are achieved in these systems. The V and Fe adsorption systems are the best candidates to produce the topological states. The k .p model calculations indicate that these topological states are determined by the TM magnetism, the C3 v crystal field from the Mo S2 substrate, and the TM atomic spin-orbit coupling (SOC). The special two-meron pseudospin texture is found to contribute to the topology. The apparent difference between the Berry curvatures for the V and Fe adsorption systems is also explored. Our results widen the understanding of the Chern insulators and are helpful for the applications of the Mo S2 monolayers in the future electronics and spintronics.

  4. Observation of an alternative χc<mn>0mn> stretchy='false'>(mo>>2mn>P stretchy='false'>)mo> candidate in e<mo>+mo>e- stretchy='false'>→mo>J stretchy='false'>/mo>ψDD<mo stretchy='false'>¯mo>

    Energy Technology Data Exchange (ETDEWEB)

    Chilikin, K.; Adachi, I.; Aihara, H.; Al Said, S.; Asner, D. M.; Aulchenko, V.; Ayad, R.; Babu, V.; Badhrees, I.; Bakich, A. M.; Bansal, V.; Barberio, E.; Besson, D.; Bhardwaj, V.; Bhuyan, B.; Biswal, J.; Bobrov, A.; Bondar, A.; Bozek, A.; Bračko, M.; Browder, T. E.; Červenkov, D.; Chekelian, V.; Chen, A.; Cheon, B. G.; Cho, K.; Choi, Y.; Cinabro, D.; Dash, N.; Di Carlo, S.; Doležal, Z.; Drásal, Z.; Dutta, D.; Eidelman, S.; Farhat, H.; Fast, J. E.; Ferber, T.; Fulsom, B. G.; Gaur, V.; Gabyshev, N.; Garmash, A.; Gillard, R.; Goldenzweig, P.; Haba, J.; Hara, T.; Hayasaka, K.; Hou, W. -S.; Inami, K.; Ishikawa, A.; Itoh, R.; Iwasaki, Y.; Jacobs, W. W.; Jaegle, I.; Jeon, H. B.; Jin, Y.; Joffe, D.; Joo, K. K.; Julius, T.; Kang, K. H.; Karyan, G.; Katrenko, P.; Kim, D. Y.; Kim, H. J.; Kim, J. B.; Kim, K. T.; Kim, M. J.; Kim, S. H.; Kim, Y. J.; Kinoshita, K.; Kodyš, P.; Korpar, S.; Kotchetkov, D.; Križan, P.; Krokovny, P.; Kuhr, T.; Kulasiri, R.; Kuzmin, A.; Kwon, Y. -J.; Lange, J. S.; Li, L.; Li Gioi, L.; Libby, J.; Liventsev, D.; Lubej, M.; Luo, T.; Masuda, M.; Matsuda, T.; Matvienko, D.; Miyabayashi, K.; Miyata, H.; Mizuk, R.; Mohanty, G. B.; Moon, H. K.; Mori, T.; Mussa, R.; Nakano, E.; Nakao, M.; Nanut, T.; Nath, K. J.; Natkaniec, Z.; Nayak, M.; Niiyama, M.; Nisar, N. K.; Nishida, S.; Ogawa, S.; Okuno, S.; Olsen, S. L.; Ono, H.; Pakhlov, P.; Pakhlova, G.; Pal, B.; Pardi, S.; Park, H.; Paul, S.; Pestotnik, R.; Piilonen, L. E.; Pulvermacher, C.; Ritter, M.; Sahoo, H.; Sakai, Y.; Salehi, M.; Sandilya, S.; Santelj, L.; Sanuki, T.; Schneider, O.; Schnell, G.; Schwanda, C.; Seino, Y.; Senyo, K.; Seon, O.; Sevior, M. E.; Shebalin, V.; Shen, C. P.; Shibata, T. -A.; Shiu, J. -G.; Sokolov, A.; Solovieva, E.; Starič, M.; Sumiyoshi, T.; Takizawa, M.; Tamponi, U.; Tanida, K.; Tenchini, F.; Trabelsi, K.; Uchida, M.; Uehara, S.; Uglov, T.; Uno, S.; Usov, Y.; Van Hulse, C.; Varner, G.; Vinokurova, A.; Vossen, A.; Wang, C. H.; Wang, M. -Z.; Wang, P.; Watanabe, M.; Watanabe, Y.; Widmann, E.; Won, E.; Yamamoto, H.; Yamashita, Y.; Ye, H.; Yuan, C. Z.; Yusa, Y.; Zhang, Z. P.; Zhilich, V.; Zhulanov, V.; Zupanc, A.

    2017-06-16

    We perform a full amplitude analysis of the process e+ e- → J/ψ$D\\bar{D}$, where D refers to either D0 or D+. A new charmoniumlike state X*(3860) that decays to$D\\bar{D}$ is observed with a significance of 6.5σ. Its mass is (3862 $+26+40\\atop{-32-13}$) MeV=c2, and its width is (201 $+154+88\\atop{-67-82}$) MeV. The JPC 0++ hypothesis is favored over the 2++ hypothesis at the level of 2.5σ.

  5. Engineering the polar magneto-optical Kerr effect in strongly strained L10-MnAl films

    Science.gov (United States)

    Zhu, Lijun; Brandt, Liane; Zhao, Jianhua

    2016-10-01

    We report the engineering of the polar magnetooptical (MO) Kerr effect in perpendicularly magnetized L10-MnAl epitaxial films with remarkably tuned magnetization, strain, and structural disorder by varying substrate temperature (T s) during molecular-beam epitaxy growth. The Kerr rotation was enhanced by a factor of up to 5 with T s increasing from 150 to 350 °C as a direct consequence of the improvement of the magnetization. A similar remarkable tuning effect was also observed on the Kerr ellipticity and the magnitude of the complex Kerr angle, while the phase of the complex Kerr angle appears to be independent of the magnetization. The combination of the good semiconductor compatibility, the moderate coercivity of 0.3-8.2 kOe, the tunable polar MO Kerr effect of up to ~0.034°, and giant spin precession frequencies of up to ~180 GHz makes L10-MnAl films a very interesting MO material. Our results give insights into both the microscopic mechanisms of the MO Kerr effect in L10-MnAl alloys and their scientific and technological application potential in the emerging spintronics and ultrafast MO modulators.

  6. 95Mo NMR: hyperfine interactions in MoO3, MoS2, MoSe2 Mo3Se4, MoSi2 and Mo2C.

    Science.gov (United States)

    Bastow, T J

    1998-10-01

    Nuclear hyperfine interactions have been obtained by nuclear magnetic resonance (NMR) for 95Mo in a number of binary Mo compounds, both insulators and metals, which illustrate the interplay between nuclear quadrupole and chemical (Knight) shift terms. The insulating phases are characterised by nuclear spin lattice relaxation times greater than 100 s, demonstrating the ineffectiveness of indirect phonon Raman relaxation for these compounds.

  7. Mercury (Hg) burden in children: The impact of dental amalgam

    Energy Technology Data Exchange (ETDEWEB)

    Al-Saleh, Iman, E-mail: iman@kfshrc.edu.sa [Biological and Medical Research Department, King Faisal Specialist Hospital and Research Centre, PO Box: 3354, Riyadh 11211 (Saudi Arabia); Al-Sedairi, Al anoud [Department of Zoology, College of Science, King Saud University, PO Box: 24452, Riyadh 11495 (Saudi Arabia)

    2011-07-15

    The risks and benefits of using mercury (Hg) in dental amalgam have long been debated. This study was designed to estimate Hg body burden and its association with dental amalgam fillings in 182 children (ages: 5-15 years) living in Taif City. Hg was measured in urine (UHg), hair (HHg) and toenails (NHg) by the Atomic Absorption Spectrophotometer with Vapor Generator Accessory system. Urinary Hg levels were calculated as both micrograms per gram creatinine ({mu}g/g creatinine) and micrograms per liter ({mu}g/L). We found that children with amalgam fillings (N = 106) had significantly higher UHg-C levels than children without (N = 76), with means of 3.763 {mu}g/g creatinine versus 3.457 {mu}g/g creatinine, respectively (P = 0.019). The results were similar for UHg (P = 0.01). A similar pattern was also seen for HHg, with means of 0.614 {mu}g/g (N = 97) for children with amalgam versus 0.242 {mu}g/g (N = 74) for those without amalgam fillings (P = 0). Although the mean NHg was higher in children without amalgam (0.222 {mu}g/g, N = 61) versus those with (0.163 {mu}g/g, N = 101), the relationship was not significant (P = 0.069). After adjusting for many confounders, the multiple logistic regression model revealed that the levels of UHg-C and HHg were 2.047 and 5.396 times higher, respectively, in children with dental amalgam compared to those without (P < 0.01). In contrast, a significant inverse relationship was seen between NHg levels and dental amalgam fillings (P = 0.003). Despite the controversy surrounding the health impact of dental amalgam, this study showed some evidence that amalgam-associated Hg exposure might be related with symptoms of oral health, such as aphthous ulcer, white patches, and a burning-mouth sensation. Further studies are needed to reproduce these findings. The present study showed that significant numbers of children with or without amalgam had Hg levels exceeding the acceptable reference limits. The detrimental neurobehavioral and

  8. Overcoming phytoremediation limitations. A case study of Hg contaminated soil

    Science.gov (United States)

    Barbafieri, Meri

    2013-04-01

    Phytoremediation is a broad term that comprises several technologies to clean up water and soil. Despite the numerous articles appearing in scientific journals, very few field applications of phytoextraction have been successfully realized. The research here reported on Phytoextraction, the use the plant to "extract" metals from contaminated soil, is focused on implementations to overcome two main drawbacks: the survival of plants in unfavorable environmental conditions (contaminant toxicity, low fertility, etc.) and the often lengthy time it takes to reduce contaminants to the requested level. Moreover, to overcome the imbalance between the technology's potential and its drawbacks, there is growing interest in the use of plants to reduce only the fraction that is the most hazardous to the environment and human health, that is to target the bioavailable fractions of metals in soil. Bioavailable Contaminant Stripping (BCS) would be a remediation approach focused to remove the bioavailable metal fractions. BCS have been used in a mercury contaminated soil from Italian industrial site. Bioavailable fractions were determined by sequential extraction with H2O and NH4Cl.Combined treatments of plant hormone and thioligand to strength Hg uptake by crop plants (Brassica juncea and Helianthus annuus) were tested. Plant biomass, evapotranspiration, Hg uptake and distribution following treatments were compared. Results indicate the plant hormone, cytokinine (CK) foliar treatment, increased evapotranspiration rate in both tested plants. The Hg uptake and translocation in both tested plants increased with simultaneous addition of CK and TS treatments. B. juncea was the most effective in Hg uptake. Application of CK to plants grown in TS-treated soil lead to an increase in Hg concentration of 232% in shoots and 39% in roots with respect to control. While H. annuus gave a better response in plant biomass production, the application of CK to plants grown in TS-treated soil lead to

  9. Bioaccumulation of Hg in the mushroom Pleurotus ostreatus

    Energy Technology Data Exchange (ETDEWEB)

    Bressa, G.; Cima, L.; Costa, P.

    1988-10-01

    The possibility of utilizing industrial, urban, and other wastes for the growth of a product which is directly edible by humans is fascinating. However, it is possible that many wastes containing toxic substances, for example, heavy metals, could reach the food chain and produce adverse effects on human health. To this end, we studied the possibility of bioaccumulation of Hg by a mushroom, Pleurotus ostreatus, grown on an artificial compost containing this element. Concentrations of 0.05, 0.1, and 0.2 mg/kg of Hg as Hg(NO/sub 3/)/sub 2/.H/sub 2/O were added to three groups of the same compost, successively inoculated with the mycelia of the mushroom. Higher concentrations strongly reduced the growth of the mycelia and therefore were not utilized. The concentrations of Hg in the substrate and in the mushroom were evaluated by AAS. The range of the accumulation factor was found to be 65-140, i.e., very marked. This finding suggests that the cultivation of P. ostreatus on substrates containing Hg from industrial and urban wastes could involve possible risks to human health.

  10. Measurements of branching fractions and time-dependent CP violating asymmetries in B<mn>0mn><mo>→D stretchy='false'>(mo>* stretchy='false'>)mo><momo>D<mo>∓> decays

    Energy Technology Data Exchange (ETDEWEB)

    Röhrken, M.; Adachi, I.; Aihara, H.; Asner, D. M.; Aulchenko, V.; Aushev, T.; Bakich, A. M.; Barrett, M.; Belous, K.; Bhardwaj, V.; Bhuyan, B.; Bischofberger, M.; Bondar, A.; Bonvicini, G.; Bozek, A.; Bračko, M.; Brovchenko, O.; Browder, T. E.; Chang, M. -C.; Chen, A.; Chen, P.; Cheon, B. G.; Chilikin, K.; Cho, I. -S.; Cho, K.; Choi, Y.; Dalseno, J.; Doležal, Z.; Drásal, Z.; Drutskoy, A.; Eidelman, S.; Fast, J. E.; Feindt, M.; Gaur, V.; Gabyshev, N.; Garmash, A.; Goh, Y. M.; Haba, J.; Hayashii, H.; Horii, Y.; Hoshi, Y.; Hou, W. -S.; Hsiung, Y. B.; Hyun, H. J.; Iijima, T.; Ishikawa, A.; Itoh, R.; Iwabuchi, M.; Iwasaki, Y.; Julius, T.; Kang, J. H.; Kawasaki, T.; Kiesling, C.; Kim, H. J.; Kim, H. O.; Kim, J. B.; Kim, J. H.; Kim, K. T.; Kim, M. J.; Kim, Y. J.; Kinoshita, K.; Ko, B. R.; Koblitz, S.; Kodyš, P.; Korpar, S.; Kouzes, R. T.; Križan, P.; Krokovny, P.; Kronenbitter, B.; Kuhr, T.; Kumita, T.; Kwon, Y. -J.; Lee, S. -H.; Li, J.; Li, Y.; Libby, J.; Liu, C.; Liu, Y.; Liu, Z. Q.; Liventsev, D.; Louvot, R.; Miyabayashi, K.; Miyata, H.; Mizuk, R.; Mohanty, G. B.; Moll, A.; Mori, T.; Muramatsu, N.; Nagasaka, Y.; Nakano, E.; Nakao, M.; Natkaniec, Z.; Nishida, S.; Nitoh, O.; Ogawa, S.; Ohshima, T.; Okuno, S.; Olsen, S. L.; Ozaki, H.; Pakhlova, G.; Park, C. W.; Park, H.; Park, H. K.; Park, K. S.; Pedlar, T. K.; Pestotnik, R.; Petrič, M.; Piilonen, L. E.; Poluektov, A.; Prim, M.; Prothmann, K.; Ritter, M.; Ryu, S.; Sahoo, H.; Sakai, Y.; Sanuki, T.; Sato, Y.; Schneider, O.; Schwanda, C.; Schwartz, A. J.; Senyo, K.; Seon, O.; Sevior, M. E.; Shapkin, M.; Shen, C. P.; Shibata, T. -A.; Shiu, J. -G.; Shwartz, B.; Sibidanov, A.; Simon, F.; Singh, J. B.; Smerkol, P.; Sohn, Y. -S.; Sokolov, A.; Solovieva, E.; Stanič, S.; Starič, M.; Sumisawa, K.; Sumiyoshi, T.; Trabelsi, K.; Uchida, M.; Uehara, S.; Unno, Y.; Uno, S.; Urquijo, P.; Vanhoefer, P.; Varner, G.; Varvell, K. E.; Vorobyev, V.; Wang, C. H.; Wang, M. -Z.; Wang, P.; Watanabe, M.; Watanabe, Y.; Williams, K. M.; Won, E.; Yamamoto, H.; Yamashita, Y.; Zander, D.; Zhang, Z. P.; Zhilich, V.; Zhulanov, V.; Zupanc, A.

    2012-05-01

    We report measurements of branching fractions and time-dependent CP asymmetries in B0→D+D- and B0→D*±D∓ decays using a data sample that contains (772±11)×106BB pairs collected at the Υ(4S) resonance with the Belle detector at the KEKB asymmetric-energy e+e- collider. We determine the branching fractions to be B(B0→D+D-)=(2.12±0.16±0.18)×10-4 and B(B0→D*±D∓)=(6.14±0.29±0.50)×10-4. We measure CP asymmetry parameters SD+D-=-1.06-0.14+0.21±0.08 and CD+D-=-0.43±0.16±0.05 in B0→D+D- and AD*D=+0.06±0.05±0.02, SD*D=-0.78±0.15±0.05, CD*D=-0.01±0.11±0.04, ΔSD*D=-0.13±0.15±0.04 and ΔCD*D=+0.12±0.11±0.03 in B0→D*±D∓, where the first uncertainty is statistical and the second is systematic. We exclude the conservation of CP symmetry in both decays at equal to or greater than 4σ significance.

  11. Mo-Si alloy development

    Energy Technology Data Exchange (ETDEWEB)

    Liu, C.T.; Heatherly, L.; Wright, J.L. [Oak Ridge National Lab., TN (United States)

    1996-06-01

    The objective of this task is to develop new-generation corrosion-resistant Mo-Si intermetallic alloys as hot components in advanced fossil energy conversion and combustion systems. The initial effort is devoted to Mo{sub 5}-Si{sub 3}-base (MSB) alloys containing boron additions. Three MSB alloys based on Mo-10.5Si-1.1B (wt %), weighing 1500 g were prepared by hot pressing of elemental and alloy powders at temperatures to 1600{degrees}C in vacuum. Microporosities and glassy-phase (probably silicate phases) formations are identified as the major concerns for preparation of MSB alloys by powder metallurgy. Suggestions are made to alleviate the problems of material processing.

  12. Ti–V–Mn based metal hydrides for hydrogen compression applications

    Energy Technology Data Exchange (ETDEWEB)

    Pickering, Lydia, E-mail: lydia.pickering@btinternet.com; Reed, Daniel; Bevan, Alexander I.; Book, David, E-mail: d.book@bham.ac.uk

    2015-10-05

    Highlights: • Ti–V–Mn based alloys were investigated as V was substituted for Nb, Cr, Mo and Ta. • The produced alloys were found to possess C14 Laves, BCC and FCC phases. • <0.2 Nb substituted for V led to small hysteresis and high dissociation pressures. • Ti{sub 0.5}–V{sub 0.45}–Nb{sub 0.05}–Mn is a suitable alloy to be used in a metal hydride compressor. - Abstract: Ti–V–Mn based alloys, consisting mainly of the hexagonal C14 Laves and BCC phases, with nominal compositions of Ti{sub 0.5}V{sub 0.4}TM{sub 0.1}Mn, where TM = Nb, Cr, Mo, Ta and Ti{sub 0.5}V{sub 0.5−x}Nb{sub x}Mn, where x = 0.05 and 0.2, were synthesised by arc melting. It was found that small amounts of Nb substituted for V (x = 0.05 and 0.1) resulted in smaller hysteresis between absorption and desorption as well as higher hydrogen dissociation pressures, compared to Ti{sub 0.5}V{sub 0.5}Mn. These findings show that Ti{sub 0.5}–V{sub 0.45}–Nb{sub 0.05}–Mn is a suitable alloy to be used in a metal hydride compressor to deliver a pressure of 650 bar in the temperature range 303–473 K.

  13. Dipole strength distribution below the giant dipole resonance in {sup 92}Mo, {sup 98}Mo and {sup 100}Mo

    Energy Technology Data Exchange (ETDEWEB)

    Rusev, G.Y.

    2006-07-01

    Investigations of the dipole-strength distributions in {sup 92}Mo, {sup 98}Mo and {sup 100}Mo were carried out by means of the method of nuclear resonance fluorescence. The low-lying excitations in the nuclides {sup 92}Mo, {sup 98}Mo and {sup 100}Mo have been studied in photon-scattering experiments at an electron energy of 6 MeV at the ELBE accelerator and at electron energies from 3.2 to 3.8 MeV at the Dynamitron accelerator. Five levels were observed in {sup 92}Mo. Five levels in {sup 98}Mo and 14 in {sup 100}Mo were identified for the first time in the energy range from 2 to 4 MeV. Dipole-strength distributions up to the neutron-separation energies in the nuclides {sup 92}Mo, {sup 98}Mo and {sup 100}Mo have been investigated at the ELBE accelerator. Because of the possible observation of transitions in the neighboring nuclei produced via ({gamma},n) reaction, additional measurements at electron energies of 8.4 and 7.8 MeV, below the neutron-separation energy, were performed on {sup 98}Mo and {sup 100}Mo, respectively. The number of transitions assigned to {sup 92}Mo, {sup 98}Mo and {sup 100}Mo is 340, 485 and 499, respectively, the main part of them being dipole transitions. Statistical properties of the observed transitions are obtained. The continuum contains the ground-state transitions as well as the branching transitions to the low-lying levels and the subsequent deexcitations of these levels. (orig.)

  14. Molybdenum depletion around P-phases Ni-Cr-Mo-W weld metals; Empobrecimento de molibdenio ao redor da fase P em metais de solda de ligas Ni-Cr-Mo-W

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Cleiton Carvalho; Miranda, Helio Cordeiro de; Farias, Jesualdo Pereira [Universidade Federal do Ceara (UFC), CE (Brazil). Departamento de Engenharia Metalurgica e de Materiais; Afonso, Conrado Ramos Moreira; Ramirez, Antonio Jose [Laboratorioo Nacional de Luz Sincroton (LNLS), SP (Brazil)

    2010-07-01

    This work evaluated the local chemical composition in matrix/precipitate interface in a Ni-Cr-Mo-W alloy weld metals deposited on substrate of C-Mn steel. The microstructural characterization was carried out through optical microscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM) and energy dispersive X-ray spectroscopy (EDS). The results had shown that the presence of secondary phases precipitates in the interdendritic region. Through SEM analysis were observed indications of depletion of Mo around these phases. These precipitates were identified as P-phase by TEM analysis. The Mo depletion indications were confirmed through EDS. The Mo depletion was a result of a reheating due to several welding heat cycles deposited to promote the coating layer. (author)

  15. Level structure of 89Mo

    Science.gov (United States)

    García-Bermúdez, G.; Cardona, M. A.; Ribas, R. V.; Filevich, A.; Achterberg, E.; Szybisz, L.

    1993-10-01

    The level structure of 89Mo has been studied with the 60Ni(32S,2pn) reaction at 110 MeV beam energy. Mainly two bands of γ rays depopulating states of probable spin-parity values ranging up to (27/2)+ were determined from the excitation function, neutron and γ-γ coincidences, and γ-ray angular distributions. The high-spin states of 89Mo show a scheme very similar to that of the 87Zr isotone. The interpretation of these states in terms of the three neutron-hole configuration (νg9/2)-3 and core-excited states is discussed.

  16. Crystal structure of Hg2SO4 – a redetermination

    Directory of Open Access Journals (Sweden)

    Matthias Weil

    2014-09-01

    Full Text Available The crystal structure of mercury(I sulfate (or mercurous sulfate, Hg2SO4, was re-determined based on modern CCD data. In comparison with the previous determination from Weissenberg film data [Dorm (1969. Acta Chem. Scand. 23, 1607–1615], all atoms were refined with anisotropic displacement parameters, leading to higher precision in terms of bond lengths and angles [e.g. Hg—Hg = 2.5031 (7 compared to 2.500 (3Å]. The structure consists of alternating rows along [001] of Hg22+ dumbbells (generated by inversion symmetry and SO42− tetrahedra (symmetry 2. The dumbbells are linked via short O—Hg—Hg—O bonds to the sulfate tetrahedra into chains extending parallel to [20-1]. More remote O—Hg—Hg—O bonds connect these chains into a three-dimensional framework.

  17. Characterization studies of purified HgI{sub 2} precursors

    Energy Technology Data Exchange (ETDEWEB)

    Schieber, M. E-mail: Schieber@vms.huji.ac.il; Zuck, A.; Sanguinetti, S.; Montalti, M.; Braiman, M.; Melekhov, L.; Nissenbaum, J.; Grilli, E.; Guzzi, M.; Turchetta, R.; Dulinski, W.; Husson, D.; Riester, J.L

    1999-06-01

    The ability of HgI{sub 2} powders, used as precursors in mercuric iodide crystal growth, to produce high-quality detectors may be predicted by non-destructive methods like photoluminescence. In fact, it is possible to correlate the presence and the intensity ratio of specific bands in the photoluminescence spectrum of a HgI{sub 2} crystal to its impurity content and stoichiometry. These quantities determine the detector grade that may be achieved using that starting material. Nine different HgI{sub 2} precursors, obtained by different purification methods, have been characterized. The lowest impurity content is achieved via poly-ethylene treatment, which gives also a powder of relatively good stoichiometric quality.

  18. Electrochemical and surface properties of nanocrystalline {beta}-MnO{sub 2} in aqueous electrolyte

    Energy Technology Data Exchange (ETDEWEB)

    Poinsignon, Christiane; Djurado, Elisabeth [LEPMI Laboratoire de Physico-Chimie des Materiaux et des Interfaces INPG ENS Electrochimie, Electrometallurgie de Grenoble UMR CNRS 5631, BP 75 F-38402 St. Martin d' Heres Cedex (France); Klein, Holger; Strobel, Pierre [Laboratoire de Cristallographie, CNRS, BP 166 Grenoble Cedex 9 (France); Thomas, Fabien [LEM Laboratoire Environnement et Mineralurgie, INPL ENS Geologie, UMR CNRS 7569, BP 40 F-54501 Vandoeuvre-les-Nancy Cedex (France)

    2006-04-01

    Surface and electrochemical properties of micrometric and nanometric tetragonal {beta}-MnO{sub 2} of, respectively, 4 and 61m{sup 2}g{sup -1} surface area were studied. The monodispersed nanocrystalline phase prepared by spray pyrolysis and characterized by transmission electron microscopy (TEM), is made of faceted crystals with 70nm x 40nm edges. Three types of energy domains were identified by surface acid-base titration. Slow step linear voltammetry reduction (10mV/2h scan rate) showed one current peak at -0.6V (versus Hg-HgO 1M KOH) for the micrometric phase, but three current peaks at -0.18, -0.36 and -0.55V for the nanometric phase. They were assigned to the reduction of: (1) surface Mn atoms related to <111> and <311> faces; (2) more stable surface Mn atoms related to <100> and <110> faces; (3) bulk Mn atoms, respectively. The presence of new reduction peaks at higher potential is ascribed to the increase in Gibbs free energy caused by the surface energy of the nanometric particle. (author)

  19. [Experimental Research of Hg (II) Removal from Aqueous Solutions of HgCl2 with Nano-TiO2].

    Science.gov (United States)

    Zhou, Xiong; Zhang, Jin-yang; Wang, Ding-yong; Qin, Cai-qing; Xu, Feng; Luo Cheng-zhong; Yang, Xi

    2016-01-15

    Mercury removal from aqueous solutions of HgCl2 was studied by indoor simulation experiments, and the effects of three different diameter of particles of Nano-TiO2 ( Nano-Titanium Dioxide) at different dosage, pH, adsorption time and the initial concentration of Hg2+ on the mercury adsorption from simulated wastewater were investigated. The single factor experiments showed that the optimal conditions were: 7.5 g x L(-1) of 5 nm TiO2 or 2.0 g x L(-1) of 100 nm TiO2, pH 8.0, initial concentration of Hg2+ 15 x mg x L(-1) adsorption time 5 min, and under these conditions the adsorption rates reached 99.5% and 99.3%, relatively. When the content of 25 nm TiO2 was 10 g x L(-1), and the other conditions were pH 8.0, initial concentration of Hg2+ 15 mg x L(-1), adsorption time 60 min, the adsorption rate was 62.8%. The Hg(II) removal effects of the TiO2 particles with different diameters followed the order of 100 nm TiO2 > 5 nm TiO2 > 25 nm TiO2. Component adsorption results showed that the 5 nm TiO2 component adsorption effect was superior to its single adsorption effect, while there was little difference between 100 nm TiO2 component adsorption effect and its single adsorption effect. The results of orthogonal experiments indicated that the influencing factors of the adsorption rate followed the order of pH > the initial concentration of Hg2+ > time > dosage. The optimal experiment scheme was: pH 8.0, a dosage of 100 nm Nano-TiO2 of 2.0 g x L(-1) an initial Hg2+ concentration of 25 mg x L(-1) and adsorption time of 10 min. Under the experimental conditions, the maximum adsorption rate reached 99.9%, at the same time, the equilibrium concentration of Hg(II) was 0.033 mg x L(-1) adsorptive capacity was 26.95 mg x g(-1). The adsorption isotherm was in line with the Langmuir isotherm equation, indicating that the Hg(II) uptake by 100 nm Nano-TiO2 was typical monolayer adsorption.

  20. Hydrothermal synthesis of alpha- and beta-HgS nanostructures

    Science.gov (United States)

    Galain, Isabel; María, Pérez Barthaburu; Ivana, Aguiar; Laura, Fornaro

    2017-01-01

    We synthesized HgS nanostructures by the hydrothermal method in order to use them as electron acceptors in hybrid organic-inorganic solar cells. We employed different mercury sources (HgO and Hg(CH3COO)2) and polyvinylpyrrolidone (PVP) or hexadecanethiol (HDT) as stabilizing/capping agent for controlling size, crystallinity, morphology and stability of the obtained nanostructures. We also used thiourea as sulfur source, and a temperature of 180 °C during 6 h. Synthesized nanostructures were characterized by powder X-Ray Diffraction, Diffuse Reflectance Infrared Fourier Transform and Transmission Electron Microscopy. When PVP acts as stabilizing agent, the mercury source has influence on the size -but not in morphology- of the beta-HgS obtained nansostructures. HDT has control over nanostructures' size and depending on the relation Hg:HDT, we obtained a mixture of alpha and beta HgS which can be advantageous in the application in solar cells, due their absorption in different spectral regions. The smallest nanostructures obtained have a mean diameter of 20 nm when using HDT as capping agent. Also, we deposited the aforementioned nanostructures onto flat glass substrates by the spin coating technique as a first approach of an active layer of a solar cell. The depositions were characterized by atomic force microscopy. We obtained smaller particle deposition and higher particle density -but a lower area coverage (5%) - in samples with HDT as capping agent. This work presents promising results on nanostructures for future application on hybrid solar cells. Further efforts will be focused on the deposition of organic-inorganic layers.

  1. Thermodynamic Stability of Transition-Metal-Substituted LiMn2-x Mx O4 (M=Cr, Fe, Co, and Ni) Spinels.

    Science.gov (United States)

    Lai, Chenying; Chen, Jiewei; Knight, James C; Manthiram, Arumugam; Navrotsky, Alexandra

    2016-07-01

    The formation enthalpies from binary oxides of LiMn2 O4 , LiMn2-x Crx O4 (x=0.25, 0.5, 0.75 and 1), LiMn2-x Fex O4 (x=0.25 and 0.5), LiMn2-x Cox O4 (x=0.25, 0.5, and 0.75) and LiMn1.75 Ni0.25 O4 at 25 °C were measured by high temperature oxide melt solution calorimetry and were found to be strongly exothermic. Increasing the Cr, Co, and Ni content leads to more thermodynamically stable spinels, but increasing the Fe content does not significantly affect the stability. The formation enthalpies from oxides of the fully substituted spinels, LiMnMO4 (M=Cr, Fe and Co), become more exothermic (implying increasing stability) with decreasing ionic radius of the metal and lattice parameters of the spinel. The trend in enthalpy versus metal content is roughly linear, suggesting a close-to-zero heat of mixing in LiMn2 O4 -LiMnMO4 solid solutions. These data confirm that transition-metal doping is beneficial for stabilizing these potential cathode materials for lithium-ion batteries.

  2. Understanding the nature of Λ<mo stretchy='false'>(mo>>1405mn> stretchy='false'>)mo> through Regge physics

    Energy Technology Data Exchange (ETDEWEB)

    Fernández-Ramírez, César; Danilkin, Igor V.; Mathieu, Vincent; Szczepaniak, Adam P.

    2016-04-01

    It appears that there are two resonances with $J^P= 1/2^-$ quantum numbers in the energy region near the $\\Lambda(1405)$ hyperon. The nature of these states is a topic of current debate. To provide further insight we use Regge phenomenology to access how these two resonances fit the established hyperon spectrum. We find that only one of these resonances is compatible with a three-quark state.

  3. Continuously increasing δ98Mo values in Neoarchean black shales and iron formations from the Hamersley Basin

    Science.gov (United States)

    Kurzweil, Florian; Wille, Martin; Schoenberg, Ronny; Taubald, Heinrich; Van Kranendonk, Martin J.

    2015-09-01

    We present Mo-, C- and O-isotope data from black shales, carbonate- and oxide facies iron formations from the Hamersley Group, Western Australia, that range in age from 2.6 to 2.5 billion years. The data show a continuous increase from near crustal δ98Mo values of around 0.50‰ for the oldest Marra Mamba and Wittenoom formations towards higher values of up to 1.51‰ for the youngest sample of the Brockman Iron Formation. Thereby, the trend in increasing δ98Mo values is portrayed by both carbonate facies iron formations and black shales. Considering the positive correlation between Mo concentration and total organic carbon, we argue that this uniformity is best explained by molybdate adsorption onto organic matter in carbonate iron formations and scavenging of thiomolybdate onto sulfurized organic matter in black shales. A temporal increase in the seawater δ98Mo over the period 2.6-2.5 Ga is observed assuming an overall low Mo isotope fractionation during both Mo removal processes. Oxide facies iron formations show lowest Mo concentrations, lowest total organic carbon and slightly lower δ98Mo compared to nearly contemporaneous black shales. This may indicate that in iron formation settings with very low organic matter burial rates, the preferential adsorption of light Mo isotopes onto Fe-(oxyhydr)oxides becomes more relevant. A similar Mo-isotope pattern was previously found in contemporaneous black shales and carbonates of the Griqualand West Basin, South Africa. The consistent and concomitant increase in δ98Mo after 2.54 billion years ago suggests a more homogenous distribution of seawater molybdate with uniform isotopic composition in various depositional settings within the Hamersley Basin and the Griqualand West Basin. The modeling of the oceanic Mo inventory in relation to the Mo in- and outflux suggests that the long-term build-up of an isotopically heavy seawater Mo reservoir requires a sedimentary sink for isotopically light Mo. The search for this

  4. Mercury (Hg) burden in children: the impact of dental amalgam.

    Science.gov (United States)

    Al-Saleh, Iman; Al-Sedairi, Al Anoud

    2011-07-15

    The risks and benefits of using mercury (Hg) in dental amalgam have long been debated. This study was designed to estimate Hg body burden and its association with dental amalgam fillings in 182 children (ages: 5-15 years) living in Taif City. Hg was measured in urine (UHg), hair (HHg) and toenails (NHg) by the Atomic Absorption Spectrophotometer with Vapor Generator Accessory system. Urinary Hg levels were calculated as both micrograms per gram creatinine (μg/g creatinine) and micrograms per liter (μg/L). We found that children with amalgam fillings (N=106) had significantly higher UHg-C levels than children without (N=76), with means of 3.763 μg/g creatinine versus 3.457 μg/g creatinine, respectively (P=0.019). The results were similar for UHg (P=0.01). A similar pattern was also seen for HHg, with means of 0.614 μg/g (N=97) for children with amalgam versus 0.242 μg/g (N=74) for those without amalgam fillings (P=0). Although the mean NHg was higher in children without amalgam (0.222 μg/g, N=61) versus those with (0.163 μg/g, N=101), the relationship was not significant (P=0.069). After adjusting for many confounders, the multiple logistic regression model revealed that the levels of UHg-C and HHg were 2.047 and 5.396 times higher, respectively, in children with dental amalgam compared to those without (Pdental amalgam fillings (P=0.003). Despite the controversy surrounding the health impact of dental amalgam, this study showed some evidence that amalgam-associated Hg exposure might be related with symptoms of oral health, such as aphthous ulcer, white patches, and a burning-mouth sensation. Further studies are needed to reproduce these findings. The present study showed that significant numbers of children with or without amalgam had Hg levels exceeding the acceptable reference limits. The detrimental neurobehavioral and/or nephrotoxic effects of such an increased Hg on children should be a cause of concern, and further investigation is warranted. Our

  5. Crystal Growth of Solid Solution HgCdTe Alloys

    Science.gov (United States)

    Lehoczky, Sandor L.

    1997-01-01

    The growth of homogenous crystals of HgCdTe alloys is complicated by the large separation between their liquidus and solidus temperatures. Hg(1-x)Cd(x)Te is representative of several alloys which have electrical and optical properties that can be compositionally tuned for a number of applications. Limitations imposed by gravity during growth and results from growth under reduced conditions are described. The importance of residual accelerations was demonstrated by dramatic differences in compositional distribution observed for different attitudes of the space shuttle that resulted in different steady acceleration components.

  6. Natural Hg isotopic composition of different Hg compounds in mammal tissues as a proxy for in vivo breakdown of toxic methylmercury.

    Science.gov (United States)

    Perrot, Vincent; Masbou, Jeremy; Pastukhov, Mikhail V; Epov, Vladimir N; Point, David; Bérail, Sylvain; Becker, Paul R; Sonke, Jeroen E; Amouroux, David

    2016-02-01

    In the last decade, specific attention has been paid to total mercury (HgT) stable isotopic composition, especially in natural samples such as aquatic organisms, due to its potential to track the cycle of this toxic element in the environment. Here, we investigated Hg Compound Specific stable Isotopic Composition (CSIC) of natural inorganic Hg (iHg) and methylmercury (MMHg) in various tissues of aquatic mammals (Beluga whale from the Arctic marine environment and seals from the freshwater lake Baikal, Russia). In seals' organs the variation in mass dependent fractionation (MDF, δ(202)Hg) for total Hg was significantly correlated to the respective fraction of iHg and MMHg compounds, with MMHg being enriched by ∼ 3‰ in heavier isotopes relative to iHg. On the other hand, we observe insignificant variation in Hg mass independent isotope fractionation (MIF, Δ(199)Hg) among iHg and MMHg in all organs for the same mammal species and MMHg in prey items. MIF signatures suggest that both MMHg and iHg in aquatic mammals have the same origin (i.e., MMHg from food), and are representative of Hg photochemistry in the water column of the mammal ecosystem. MDF signatures of Hg compounds indicate that MMHg is demethylated in vivo before being stored in the muscle, and the iHg formed is stored in the liver, and to a lesser extent in the kidney, before excretion. Thus, Hg CSIC analysis in mammals can be a powerful tool for tracing the metabolic response to Hg exposure.

  7. Electrochemical performance of co-doped Li1.2Mn0.6Ni0.2O2 cathode materials

    CSIR Research Space (South Africa)

    David, K

    2013-04-01

    Full Text Available The composite material has a xLi2MnO 3·(1-x)LiMO2 (M = Mn, Co, Ni) structure has been considered as one of the most promising cathode materials for advanced lithium-ion batteries due to their low-cost and high capacity (> 200 mAh g−1) between 4.8 V...

  8. Controlling magnetism of MoS2 sheets by embedding transition-metal atoms and applying strain.

    Science.gov (United States)

    Zhou, Yungang; Su, Qiulei; Wang, Zhiguo; Deng, Huiqiu; Zu, Xiaotao

    2013-11-14

    Prompted by recent experimental achievement of transition metal (TM) atoms substituted in MoS2 nanostructures during growth or saturating existing vacancies (Sun et al., ACS Nano, 2013, 7, 3506; Deepak et al., J. Am. Chem. Soc., 2007, 129, 12549), we explored, via density functional theory, the magnetic properties of a series of 3d TM atoms substituted in a MoS2 sheet, and found that Mn, Fe, Co, Ni, Cu and Zn substitutions can induce magnetism in the MoS2 sheet. The localizing unpaired 3d electrons of TM atoms respond to the introduction of a magnetic moment. Depending on the species of TM atoms, the substituted MoS2 sheet can be a metal, semiconductor or half-metal. Remarkably, the applied elastic strain can be used to control the strength of the spin-splitting of TM-3d orbitals, leading to an effective manipulation of the magnetism of the TM-substituted MoS2 sheet. We found that the magnetic moment of the Mn- and Fe-substituted MoS2 sheets can monotonously increase with the increase of tensile strain, while the magnetic moment of Co-, Ni-, Cu- and Zn-substituted MoS2 sheets initially increases and then decreases with the increase of tensile strain. An instructive mechanism was proposed to qualitatively explain the variation of magnetism with elastic strain. The finding of the magnetoelastic effect here is technologically important for the fabrication of strain-driven spin devices on MoS2 nanostructures, which allows us to go beyond the current scope limited to the spin devices within graphene and BN-based nanostructures.

  9. Pre-edge features in X-ray absorption structure of Mn in GaMnN, GaMnAs and GeMn

    Energy Technology Data Exchange (ETDEWEB)

    Titov, A. [A.M. Prokhorov General Physics Institute, Russian Academy of Sciences, Vavilov str. 38, 119991 Moscow (Russian Federation) and ' Nanophysique et Semiconducteurs' , CEA-CNRS-Universite Joseph Fourier Grenoble, Laboratoire de Spectrometrie Physique, BP 87, 38402 St Martin d' Heres cedex (France)]. E-mail: titov@nsc.gpi.ru; Kulatov, E. [A.M. Prokhorov General Physics Institute, Russian Academy of Sciences, Vavilov str. 38, 119991 Moscow (Russian Federation); Uspenskii, Yu.A. [Lebedev Physical Institute, Russian Academy of Sciences, Leninskii prosp. 53, 119991 Moscow (Russian Federation); Biquard, X. [DRFMC-SP2M, CEA Grenoble-38054 Grenoble cedex 9 (France); Halley, D. [' Nanophysique et Semiconducteurs' , CEA-CNRS-Universite Joseph Fourier Grenoble, Laboratoire de Spectrometrie Physique, BP 87, 38402 St Martin d' Heres cedex (France); Kuroda, S. [' Nanophysique et Semiconducteurs' , CEA-CNRS-Universite Joseph Fourier Grenoble, Laboratoire de Spectrometrie Physique, BP 87, 38402 St Martin d' Heres cedex (France); Bellet-Amalric, E. [' Nanophysique et Semiconducteurs' , CEA-CNRS-Universite Joseph Fourier Grenoble, Laboratoire de Spectrometrie Physique, BP 87, 38402 St Martin d' Heres cedex (France); DRFMC-SP2M, CEA Grenoble-38054 Grenoble cedex 9 (France); Mariette, H. [' Nanophysique et Semiconducteurs' , CEA-CNRS-Universite Joseph Fourier Grenoble, Laboratoire de Spectrometrie Physique, BP 87, 38402 St Martin d' Heres cedex (France); Cibert, J. [Laboratoire Louis Neel, CNRS, BP 166, 38042 Grenoble cedex 9 (France)

    2006-05-15

    Ga{sub 1-x}Mn{sub x}N samples with a wide range of concentrations, from x=0.003 to 0.057, were grown by molecular beam epitaxy. X-ray diffraction and the simulation of the extended X-ray absorption fine structure (EXAFS) confirmed the wurtzite structure of the samples, without any secondary phase, and the location of Mn in the gallium sublattice of GaN. The valence state of Mn was studied using the X-ray absorption near-edge structure (XANES) at the K-edge of Mn. The shape of the measured XANES spectra does not depend on the Mn concentration: that implies the same valence state and local atomic structure around the Mn atom in all samples. A calculation of the electronic band structure of GaMnN, GaMnAs, GeMn and the XANES spectra of Mn in GaMnN was performed using the linearized augmented plane wave (LAPW) method. The calculated spectra fit well our experimental data. In particular, the comparison demonstrates that a peak in the pre-edge structure is directly related to the 3+ valence state of Mn. This was confirmed experimentally by measurements of the Mn K-edge in GaMn{sup 2+}As and ZnMn{sup 2+}Te. An application of proposed interpretation for GeMn is discussed.

  10. SrMnII2MnIII(PO43

    Directory of Open Access Journals (Sweden)

    Ghaleb Alhakmi

    2013-09-01

    Full Text Available The title compound, strontium trimanganese tris(orthophosphate, was synthesized under hydrothermal conditions. Its structure is isotypic to that of the lead analogue PbMnII2MnIII(PO43. Two O atoms are in general positions, whereas all others atoms are in special positions. The Sr and one P atom exhibit mm2 symmetry, the MnII atom 2/m symmetry, the MnIII atom and the other P atom .2. symmetry and two O atoms are located on mirror planes. The three-dimensional network of the crystal structure is made up of two types of chains running parallel to [010]. One chain is linear and is composed of alternating MnIIIO6 octahedra and PO4 tetrahedra sharing vertices; the other chain has a zigzag arrangement and is built up from two edge-sharing MnIIO6 octahedra connected to PO4 tetrahedra by edges and vertices. The two types of chains are linked through PO4 tetrahedra, leading to the formation of channels parallel to [100] and [010] in which the SrII ions are located. They are surrounded by eight O atoms in the form of a slightly distorted bicapped trigonal prism.

  11. Pr16Mo21O56

    Directory of Open Access Journals (Sweden)

    Patrick Gougeon

    2011-05-01

    Full Text Available The structure of hexadecapraseodymium henicosamolybdenum hexapentacontaoxide, Pr16Mo21O56, is isotypic with other rare earth representatives of formula type RE16Mo21O56 (RE = La, Ce, Nd. It is characterized by Mo10O18iO8a units (where i = inner and a = apical O atoms containing bioctahedral Mo10 clusters and octahedral MoO6 units that share some of their O atoms to form the Mo–O framework. The two independent Mo10 cluster units are centred at Wyckoff positions 2b and 2c and have point-group symmetry overline{1}. The Mo atom of the MoO6 unit is likewise situated at an inversion centre (2d. The eight crystallographically different Pr3+ cations occupy irregular voids in the framework with coordination numbers to the O atoms varying between 8 and 11.

  12. Variations in stable isotope fractionation of Hg in food webs of Arctic lakes.

    Science.gov (United States)

    Gantner, Nikolaus; Hintelmann, Holger; Zheng, Wang; Muir, Derek C

    2009-12-15

    Biotic and abiotic fractionation of mercury (Hg) isotopes has recently been shown to occur in aquatic environments. We determined isotope ratios (IRs) of Hg in food webs (zooplankton, chironomids, Arctic char) and sediments of 10 Arctic lakes from four regions and investigated the extent of Hg isotope fractionation. Hg IRs were analyzed by multicollector inductively coupled plasma mass spectrometry (MC-ICP/MS). Hg mass independent fractionation (MIF; Delta(199)Hg) and mass dependent fractionation (MDF; delta(202)Hg) were calculated and compared among samples. IRs of Hg in sediment were characterized mainly by MDF and low MIF (Delta(199)Hg -0.37 to 0.74 per thousand). However, all biota showed evidence of MIF, most pronounced in zooplankton (Delta(199)Hg up to 3.40 per thousand) and char (Delta(199)Hg up to 4.87 per thousand). Zooplankton takes up highly fractionated MeHg directly from the water column, while benthic organisms are exposed to sedimentary Hg, which contains less fractionated Hg. As evidenced by delta(13)C measurements, benthic chironomids make up a large proportion of char diet, explaining in part why MIF(char) meteor impact crater lake (Pingualuk) reflects a "pure" atmospheric Hg signature, which is modified only by aqueous in-lake processes. All other lakes are also affected by terrestrial Hg inputs and sediment processes.

  13. Conductive reduced graphene oxide/MnO2 carbonized cotton fabrics with enhanced electro -chemical, -heating, and -mechanical properties

    Science.gov (United States)

    Tian, Mingwei; Du, Minzhi; Qu, Lijun; Zhang, Kun; Li, Hongliang; Zhu, Shifeng; Liu, Dongdong

    2016-09-01

    Versatile and ductile conductive carbonized cotton fabrics decorated with reduced graphene oxide (rGO)/manganese dioxide (MnO2) are prepared in this paper. In order to endow multifunction to cotton fabric, graphene oxide (GO) is deposited on cotton fibers by simple dip-coating route. MnO2 nanoparticles are assembled on the surface of cotton fabric through in-situ chemical solution deposition. MnO2/GO@cotton fabrics are carbonized to achieve conductive fabric (MnO2/rGO@C). The morphologies and structures of obtained fabrics are characterized by SEM, XRD, ICP and element analysis, and their electro-properties including electro-chemical, electro-heating and electro-mechanical properties are evaluated. The MnO2/rGO@C yields remarkable specific capacitance of 329.4 mA h/g at the current density of 100 mA/g, which is more than 40% higher than that of the control carbonized cotton fabric (231 mA h/g). Regarding electro-heating properties, the temperature of MnO2/rGO@C fabric could be monotonically increased to the steady-state maximum temperatures (ΔTmax) of 36 °C within 5 min under the applied voltage 15 V while the ΔTmax = 17 °C of the control case. In addition, MnO2/rGO@C exhibits repeatable electro-mechanical properties and its normalized resistance (R-R0)/R0 could reach 0.78 at a constant strain (curvature = 0.6 cm-1). The MnO2/rGO@C fabric is versatile, scalable, and adaptable to a wide variety of smart textiles applications.

  14. Thermomechanical Processing and Texture Development in Ni-Cr-Mo and Mn-Mo-B Armor Steels

    Science.gov (United States)

    1984-04-01

    bainite transformations; and (3) 900*F (482 0 C), a temperature which corresponds roughly to the nose of upper bainite trans- formation. Various...also indi- cated by the amounts of upper bainite formation, although to a lesser degree, in these two steels. These observations are con- sistent with...grain boundaries. 1 3 ) The some- what lesser retarding effect for upper bainite transformation is also consistent with the above interpretation

  15. Optimization of the Processing of Mo Disks

    Energy Technology Data Exchange (ETDEWEB)

    Tkac, Peter [Argonne National Lab. (ANL), Argonne, IL (United States); Rotsch, David A. [Argonne National Lab. (ANL), Argonne, IL (United States); Stepinski, Dominique [Argonne National Lab. (ANL), Argonne, IL (United States); Makarashvili, Vakhtang [Argonne National Lab. (ANL), Argonne, IL (United States); Harvey, James [NorthStar Medical Technologies, LLC, Madison, WI (United States); Vandegrift, George F. [Argonne National Lab. (ANL), Argonne, IL (United States)

    2016-01-01

    The objective of this work is to decrease the processing time for irradiated disks of enriched Mo for the production of 99Mo. Results are given for the dissolution of nonirradiated Mo disks, optimization of the process for large-scale dissolution of sintered disks, optimization of the removal of the main side products (Zr and Nb) from dissolved targets, and dissolution of irradiated Mo disks.

  16. 46 CFR 53.01-5 - Scope (modifies HG-100).

    Science.gov (United States)

    2010-10-01

    ... Shipping COAST GUARD, DEPARTMENT OF HOMELAND SECURITY (CONTINUED) MARINE ENGINEERING HEATING BOILERS General Requirements § 53.01-5 Scope (modifies HG-100). (a) The regulations in this part apply to steam heating boilers, hot water boilers (which include hot water heating boilers and hot water supply...

  17. Decay from the superdeformed bands in {sup 194}Hg

    Energy Technology Data Exchange (ETDEWEB)

    Henry, R.G.; Khoo, T.L.; Carpenter, M.P. [and others

    1995-08-01

    Superdeformed bands in {sup 194}H g were studied using the early implementation of Gammasphere. The response functions for the Ge detectors were measured for the first time as part of this experiment. Experiments were performed with both a backed target (where the residue stopped in the Au backing) and a thin target (where the residue recoiled into vacuum). This will permit measurements of the decay times of the quasicontinuum {gamma}rays. The spectrum in coincidence with the yrast SD band in {sup 194}Hg reveals the same features as found in the quasicontinuum structure in {sup 192}Hg. These features include: statistical {gamma}rays feeding the SD band, a pronounced E2 peak from transitions feeding the SD band, a Ml/E2 bump at low energies that is associated with the last stages of feeding of the superdeformed band, and a quasicontinuous distribution from {gamma}rays linking SD and normal states, including a sizable clustering of strength around 1.7 MeV. The remarkable similarity of the spectra coincident with SD bands in {sup 192,194}Hg provides additional support for a statistical process for decay out of the SD states. This similarity contrasts with differences observed in the spectrum coincident with the SD band in the odd-even {sup 191}Hg, confirming the predictions about the role of pairing (in normal states) in influencing the shape of the decay-out spectrum.

  18. Emission and gain studies of the Tl-Hg excimer

    Energy Technology Data Exchange (ETDEWEB)

    Chilukuri, S.; Nayfeh, M.H.

    1978-11-01

    The pressure and temperature dependence of the Tl-Hg excimer emission in the visible from an rf excited discharge has been studied. The gain of the system in the blue band at 4585 A is probed with an Ar-ion laser. With gain sensitivity limited to 1/2% due to beam steering and defocusing effects, the system has no gain.

  19. Hypotension is 100 mm Hg on the Battlefield

    Science.gov (United States)

    2011-10-01

    corroborate the predictive value of admission metabolic acidosis on patient survival. We also were able to show that an SBP of 110 mm Hg after injury was... metabolic acidosis , complications, length of stay, intensive care unit days, and ventilator days all increased. The implication of our result suggested

  20. Experimental study of 199Hg spin anti-relaxation coatings

    CERN Document Server

    Chowdhuri, Z; Horras, M; Kirch, K; Krempel, J; Lauss, B; Mtchedlishvili, A; Rebreyend, D; Roccia, S; Schmidt-Wellenburg, P; Zsigmond, G

    2013-01-01

    We report on a comparison of spin relaxation rates in a $^{199}$Hg magnetometer using different wall coatings. A compact mercury magnetometer was built for this purpose. Glass cells coated with fluorinated materials show longer spin coherence times than if coated with their hydrogenated homologues. The longest spin relaxation time of the mercury vapor was measured with a fluorinated paraffin wall coating.

  1. Ion Beam Nanostructuring of HgCdTe Ternary Compound

    Science.gov (United States)

    Smirnov, Aleksey B.; Savkina, Rada K.; Udovytska, Ruslana S.; Gudymenko, Oleksandr I.; Kladko, Vasyl P.; Korchovyi, Andrii A.

    2017-05-01

    Systematic study of mercury cadmium telluride thin films subjected to the ion beam bombardment was carried out. The evolution of surface morphology of (111) Hg1 - x Cd x Te ( x 0.223) epilayers due to 100 keV B+ and Ag+ ion irradiation was studied by AFM and SEM methods. X-ray photoelectron spectroscopy and X-ray diffraction methods were used for the investigation of the chemical compound and structural properties of the surface and subsurface region. It was found that in the range of nanoscale, arrays of holes and mounds on Hg0.777Cd0.223Te (111) surface as well as the polycrystalline Hg1 - x Cd x Te cubic phase with alternative compound ( x 0.20) have been fabricated using 100 keV ion beam irradiation of the basic material. Charge transport investigation with non-stationary impedance spectroscopy method has shown that boron-implanted structures are characterized by capacity-type impedance whereas for silver-implanted structures, an inductive-type impedance (or "negative capacitance") is observed. A hybrid system, which integrates the nanostructured ternary compound (HgCdTe) with metal-oxide (Ag2O) inclusions, was fabricated by Ag+ ion bombardment. The sensitivity of such metal-oxide-semiconductor hybrid structure for sub-THz radiation was detected with NEP 4.5 × 10-8 W/Hz1/2at ν ≈ 140 GHz and 296 K without amplification.

  2. Thermodynamics limits the reactivity of BrHg radical with volatile organic compounds

    Science.gov (United States)

    Dibble, Theodore S.; Schwid, Abraham C.

    2016-08-01

    Mercury emissions to the atmosphere primarily consist of Hg(0), which tends not to enter ecosystems until it is oxidized. Atomic bromine initiates oxidation of Hg(0) via the BrHg intermediate, but the further reactions of BrHg are just beginning to be explored. Here we use quantum chemistry to determine that hydrogen abstraction from hydrocarbons by BrHg is so endothermic as to be irrelevant. Bonds between BrHg and carbon atoms are so weak that BrHg addition to carbon-carbon double bonds atoms will be somewhat ineffective in leading to further reactions.

  3. Isotopic Composition of Gaseous Elemental Mercury (Hg0) at Various Sites in Japan

    Science.gov (United States)

    Yamakawa, A.; Moriya, K.; Yoshinaga, J.

    2015-12-01

    Mercury (Hg) is a toxic heavy metal, which exists in various chemical forms in the environmental system. In the atmosphere, Hg exists in three forms (Hg0(g), Hg+2(g), and Hg(p)). Hg0(g) is the dominant species of atmospheric Hg, accounting for >95% of the total Hg in the atmosphere. Because Hg0(g) is highly volatile and has limited solubility in water, it cannot be easily removed by wet or dry deposition processes. Therefore, the residence time of Hg0(g) in the atmosphere is relatively long (1 to 2 years), allowing long-range transport from mercury emission source(s). Conversely, Hg+2(g) and Hg(p) are effectively removed from the atmosphere through wet and dry depositions. The determination of mercury source attribution using quantitative data is challenging because Hg0(g) may be deposited on an area upon oxidation to Hg+2(g) and associated with aerosols and particulates to form Hg(p) while the global cycling of Hg0(g). Over the last decade, the development of analytical methods of highly precise Hg isotopic measurements demonstrated mass-dependent fractionation (MDF) and mass-independent fractionation (MIF) of Hg isotopes in environmental samples. For instance, MDF of Hg isotopes is thought to occur during various natural and industrial Hg transformations. MIF of Hg isotopes is observed during abiotic reduction, photochemical and non-photochemical, and physical and chemical processes. Such processes lead to differences in the Hg isotopic composition of different emission sources, both natural and anthropogenic, and atmospheric processes (i.e., transportation, oxidation/reduction, deposition, and reemission). Therefore, Hg isotopic compositions could be used to trace the sources and processes of atmospheric Hg. For securing the reliability and accuracy of atmospheric Hg isotope data, the methods of collection, pretreatment, and isotopic measurement for Hg0(g) were developed to obtain high recovery yield of samples with no Hg isotopic fractionation during each

  4. Importance of Dissolved Neutral Hg-Sulfides, Energy Rich Organic Matter and total Hg Concentrations for Methyl Mercury Production in Sediments

    Science.gov (United States)

    Drott, A.; Skyllberg, U.

    2007-12-01

    Methyl mercury (MeHg) is the mercury form that biomagnifies to the greatest extent in aquatic food webs. Therefore information about factors determining MeHg concentrations is critical for accurate risk assessment of contaminated environments. The concentration of MeHg in wetlands and sediments is the net result of: 1) methylation rates, 2) demethylation rates, and 3) input/output processes. In this study, the main controls on Hg methylation rates and total concentrations of MeHg, were investigated at eight sites in Sweden with sediments that had been subjected to local Hg contamination either as Hg(0), or as phenyl-Hg. Sediments were selected to represent a gradient in total Hg concentration, temperature climate, salinity, primary productivity, and organic C content and quality. Most sediments were high in organic matter content due to wood fibre efflux from pulp and paper industry. The pore water was analysed for total Hg, MeHg, DOC, H2S(aq), pH, DOC, Cl and Br. The chemical speciation of Hg(II) and MeHg in pore water was calculated using equilibrium models. Potential methylation and demethylation rates in sediments were determined in incubation experiments at 23° C under N2(g) for 48 h, after addition of isotopically enriched 201Hg(II) and Me204Hg. In all surface (0-20 cm) sediments there was a significant (pproduction overruled degradation and input/output processes of MeHg in surface sediments, and that % MeHg in surface sediments may be used as a proxy for net production of MeHg. To our knowledge, these are the first data showing significant positive relationships between short term (48 h) MeHg production and longer term accumulation of MeHg, across a range of sites with different properties (1). If MeHg was not normalized to total Hg, the relationship was not significant. For sub-sets of brackish waters (pproductivity freshwaters (pproductivity freshwater (p=0.048, n=6), the sum of neutral Hg-sulfides [Hg(SH)20 (aq)] and [HgS0 (aq)] in the sediment pore

  5. Growth, properties and applications of HgCdTe

    Science.gov (United States)

    Schmit, J. L.

    1983-12-01

    This paper provides primarily a review of the methods used to grow HgCdTe with a summary of some of its basic properties and applications. Methods of crystal growth fall generally into three classes: growth from the melt, from solution and from the vapor phase. All three methods have been and are being used to grow HgCdTe. The high vapor pressure of HgCdTe at the melting point, combined with a large segregation coefficient, have effectively limited the use of Czochralski or zone melting techniques, but two melt growth techniques have survived: (1) a variation of Bridgman growth called quench-anneal wherein a dendritic crystal is formed by quenching the melt and is homogenized by solid state recrystallization below the melting point, (2) a variation of freezing from a large volume called slush-growth wherein a melt is held in a temperature gradient for several weeks while a crystal grows. Growth from solution has taken the form of liquid phase epitaxy (LPE) on CdTe with the LPE systems including growth from Hg-rich, HgTe-rich and Te-rich solutions and using tipping, vertical dipping, vertical sliding and horizontal sliding. Vapor phase growth is very promising but is not yet in production. Techniques include growth by isothermal close spaced epitaxy in which HgTe is transported isothermally by chemical potential onto CdTe, molecular beam epitaxy (MBE) in which elements are evaporated in a high vacuum, and metal organic chemical vapor deposition (MOCVD) in which some of the metal atoms are carried to the substrate bound to organic radicals before being freed by pyrolysis. In all these methods, control of Hg pressure is a major concern. The fundamental properties discussed briefly are those of prime interest to detector manufacturers: energy gap ( Eg), intrinsic carrier concentration ( ni), and electrical activity of dopants. A reasonable fit to the Eg data from ˜ 20 papers is given by Eg = -0.302+1.93x+5.35×10 -4T(1-2x)-0.810x 2+0.832x 3. This gap, combined with k

  6. Formation of PdHg by reaction of palladium thin film contacts deposited onto mercuric iodide ({alpha}-HgI{sub 2}) radiation detector crystals

    Energy Technology Data Exchange (ETDEWEB)

    Medlin, D.L. [Sandia National Labs., Livermore, CA (United States); Van Scyoc, J.M. [Carnegie-Mellon Univ., Pittsburgh, PA (United States). Dept. of Electrical and Computer Engineering; Gilbert, T.S. [Carnegie-Mellon Univ., Pittsburgh, PA (United States). Dept. of Electrical and Computer Engineering; Schlesinger, T.E. [Carnegie-Mellon Univ., Pittsburgh, PA (United States). Dept. of Electrical and Computer Engineering; Boehme, D. [Sandia National Labs., Livermore, CA (United States); Schieber, M. [Sandia National Labs., Livermore, CA (United States); Natarajan, M. [TN Technologies, Inc., Round Rock, TX (United States); James, R.B. [Sandia National Labs., Livermore, CA (United States)

    1996-10-01

    The microstructure and phase distribution of palladium thin films sputter deposited onto {alpha}-HgI{sub 2} for use as electrical contacts in radiation detectors are investigated using electron microscopy. Our results show a limited reaction to form palladium mercuride (PdHg). It is shown that the formation of PdHg via several reaction pathways is thermodynamically feasible. (orig.).

  7. QTAIM analysis of the bonding in Mo-Mo bonded dimolybdenum complexes.

    Science.gov (United States)

    Van der Maelen, Juan F; Cabeza, Javier A

    2012-07-02

    A number of local and integral topological parameters of the electron density of relevant bonding interactions in the binuclear molybdenum complexes [Mo(2)Cl(8)](4-), [Mo(2)(μ-CH(3)CO(2))(4)], [Mo(2)(μ-CF(3)CO(2))(4)], [Mo(2)(μ-CH(3)CO(2))(4)Br(2)](2-), [Mo(2)(μ-CF(3)CO(2))(4)Br(2)](2-), [Mo(2)(μ-CH(3)CO(2))(2)Cl(4)](2-), [Mo(2)(μ-CH(3)CO(2))(2)(μ-Cl)(2)Cl(4)](2-), and [Mo(2)(μ-Cl)(3)Cl(6)](3-) have been calculated and interpreted under the perspective of the quantum theory of atoms in molecules (QTAIM). These data have allowed a comparison between related but different atom-atom interactions, such as different Mo-Mo formal bond orders, ligand-unbridged versus Cl-bridged, CH(3)CO(2)-bridged, and CF(3)CO(2)-bridged Mo-Mo interactions, and Mo-Cl(terminal) and Mo-Cl(bridge) versus Mo-Br and Mo-O interactions. Calculations carried out using nonrelativistic and relativistic approaches afforded similar results.

  8. Effect of solution hardening on the shape memory effect of Fe-Mn based alloys

    Energy Technology Data Exchange (ETDEWEB)

    Tsuzaki, K.; Natsume, Y.; Maki, T. [Kyoto Univ. (Japan). Dept. of Materials Science and Engineering; Tomota, Y. [Ibaraki Univ., Hitachi (Japan)

    1995-10-01

    Fe-high Mn-Si alloys, which undergo {gamma} (fcc) to {var_epsilon} (hcp) martensitic transformation, exhibit a pronounced shape memory effect. The origin of shape memory effect of these alloys is the reversion of stress-induced {var_epsilon} martensite. A shape change must hence be accomplish3ed by stress-induced martensitic transformation without permanent slip in austenite ({gamma}) in order to obtain a good shape memory effect. It is clear that the intrusion of permanent slip can be suppressed by increasing the strength of austenite and by decreasing the applied stress required for a shape change due to stress-induced martensitic transformation. It has been reported that the addition of the interstitial elements of C and N as well as the substitutional elements of Mo and V increases the 0.2% proof stress of austenite in Fe-high Mn alloys. However, there have been few studies on the effect of these alloying elements on the shape memory effect of Fe-high Mn based alloys. In the present study, it was aimed to improve the shape memory effect of Fe-high Mn based alloys by the strengthening of austenite through solution hardening due to C and Mo.

  9. Pre-edge features in X-ray absorption structure of Mn in GaMnN, GaMnAs and GeMn

    Science.gov (United States)

    Titov, A.; Kulatov, E.; Uspenskii, Yu. A.; Biquard, X.; Halley, D.; Kuroda, S.; Bellet-Amalric, E.; Mariette, H.; Cibert, J.

    2006-05-01

    Ga1-xMnxN samples with a wide range of concentrations, from x=0.003 to 0.057, were grown by molecular beam epitaxy. X-ray diffraction and the simulation of the extended X-ray absorption fine structure (EXAFS) confirmed the wurtzite structure of the samples, without any secondary phase, and the location of Mn in the gallium sublattice of GaN. The valence state of Mn was studied using the X-ray absorption near-edge structure (XANES) at the K-edge of Mn. The shape of the measured XANES spectra does not depend on the Mn concentration: that implies the same valence state and local atomic structure around the Mn atom in all samples. A calculation of the electronic band structure of GaMnN, GaMnAs, GeMn and the XANES spectra of Mn in GaMnN was performed using the linearized augmented plane wave (LAPW) method. The calculated spectra fit well our experimental data. In particular, the comparison demonstrates that a peak in the pre-edge structure is directly related to the 3+ valence state of Mn. This was confirmed experimentally by measurements of the Mn K-edge in GaMnAs and ZnMnTe. An application of proposed interpretation for GeMn is discussed.

  10. Comparison of the characteristics and mechanisms of Hg(II) sorption by biochars and activated carbon.

    Science.gov (United States)

    Xu, Xiaoyun; Schierz, Ariette; Xu, Nan; Cao, Xinde

    2016-02-01

    Two biochars were produced from bagasse and hickory chips (referred to as BB and HCB, respectively) and evaluated for their sorption ability of Hg(II) in aqueous solution. A commercial activated carbon (AC) which is commonly used for Hg(II) removal was included for comparison. Both biochars showed higher sorption capacities than AC, following the trend of BB>HCB>AC. The sorption of Hg(II) by BB and AC was mainly attributed to the formation of (COO)2Hg(II) and (O)2Hg(II). As a result, the adsorption capacity of Hg(II) by BB decreased 17.6% and 37.6% after COOH and OH were blocked, respectively and that of Hg(II) by AC decreased 6.63% and 62.2% for COOH and OH hindered, respectively. However, blocking the function groups had little effect on the Hg removal by HCB since sorption of Hg(II) by HCB was mainly resulted from the π electrons of CC and CO induced Hg-π binding. Further X-ray photoelectron spectroscopy analysis indicated the possibility of reduction of the Hg(II) to Hg(I) by phenol groups or π electrons during the removal of Hg(II) by both biochars. In conclusion, biochar is more effective than activated carbon in removing Hg(II) and there exists a high potential that biochar can be a substitute of activated carbon for removal of Hg(II) from wastewater.

  11. Beer Law Constants and Vapor Pressures of HgI2 over HgI2(s,l)

    Science.gov (United States)

    Su, Ching-Hua; Zhu, Shen; Ramachandran, N.; Burger, A.

    2002-01-01

    Optical absorption spectra of the vapor phase over HgI2(s,l) were measured at sample temperatures between 349 and 610 K for wavelengths between 200 and 600 nm. The spectra show the samples sublimed congruently into HGI2 without any observed Hg or I2 absorption spectra. The Beer's Law constants for 15 wavelengths between 200 and 440 nm were derived. From these constants the vapor pressure of HgI2, P, was found to be a function of temperature for the liquid and the solid beta-phases: ln P(atm) = -7700/T(K) + 12.462 (liquid phase) and ln P(atm) = -10150/T(K) + 17.026 (beta-phase). The expressions match the enthalpies of vaporization and sublimation of 15.30 and 20.17 kcal/mole respectively, for the liquid and the beta-phase HgI2. The difference in the enthalpies gives an enthalpy of fusion of 4.87 kcal/mole, and the intersection of the two expressions gives a melting point of 537 K.

  12. Cavitation Erosion Behavior of CrMnN Duplex Stainless Steel in Distilled Water and 3% NaCl Solution

    Institute of Scientific and Technical Information of China (English)

    Suzhen LUO; Yugui ZHENG; Wei LIU; Heming JING; Zhiming YAO; Wei KE

    2003-01-01

    The cavitation erosion (CE) behavior of CrMnN ferrite-austenite duplex stainless steel in distilled water and 3% NaCl solution was investigated by using a magnetostrictive-induced CE facility. The damaged surfaces were observed by scanning electron microscope (SEM). It was found that the CE resistance of CrMnN steel was higher than that of 0Cr13Ni5Mo steel. The mass loss rate of CrMnN steel in distilled water was similar to that in 3% NaCl except at the early stage of CE. The failure mode of ferrite phase was brittle fracture, which had adverse effect on the resistance to CE, while the failure of austenite phase was a ductile failure in CrMnN steel. The excellent resistance to CE was related to the good mechanical properties of austenitic phase and the consumption of CE energy by plastic deformation involving slip and twinning.

  13. Synthesis of hierarchical MoO2/MoS2 nanofibers for electrocatalytic hydrogen evolution

    Science.gov (United States)

    Rheem, Youngwoo; Han, Yosep; Lee, Kyu Hwan; Choi, Sung-Mook; Myung, Nosang V.

    2017-03-01

    Perpendicularly attached MoS2 nanosheets on MoO2 conductive nanofibers were synthesized by combining electrospinning, calcination, and sulfurization processes. Compared to randomly stacked MoS2 nanosheets on MoO2 nanofiber, they show greater hydrogen evolution reaction (HER) performance (i.e., onset potential of ‑180 mV versus normal hydrogen electrode with the Tafel slope of 59 mV dec‑1). HER performance decreases with increasing MoS2 nanocrystal size.

  14. High-spin Mn wheels.

    Science.gov (United States)

    Manoli, Maria; Prescimone, Alessandro; Bagai, Rashmi; Mishra, Abhudaya; Murugesu, Muralee; Parsons, Simon; Wernsdorfer, Wolfgang; Christou, George; Brechin, Euan K

    2007-08-20

    The syntheses, structures, and magnetic properties of the complexes [MnIV4MnIII10MnII2O2(OCH3)12(tmp)8(O2CCH3)10].3Et2O (1.3Et2O), [MnIV2MnIII18MnII2O6(OCH3)14(O2CCH3)16(tmp)8(HIm)2].2CH3OH (2.2CH3OH), and [MnIV2MnIII18MnII2O6(OCH3)14(O2CCH3)16(Br-mp)8(HIm)2].2C6H14.5CH3OH (3.2C6H14.5CH3OH) are reported. The unusual wheel-like complexes were prepared by the treatment of [Mn3O(O2CCH3)6(HIm)3](O2CCH3) (HIm = imidazole) with 1,1,1-tris-(hydroxymethyl)propane (H3tmp) (1 and 2) or 2-(bromomethyl)-2-(hydroxymethyl)-1,3-propanediol (Br-mpH3) (3) in the presence of sodium methoxide (NaOCH3, 2, and 3) in CH3OH. Complex 1.3Et2O crystallizes in the triclinic space group P, while complexes 2.2CH3OH and 3.2C6H14.5CH3OH crystallize in the orthorhombic space group Pbca. Direct current magnetic susceptibility data, collected for 1-3 in the respective 1.8-300 K and 0.1-7 T temperature and magnetic-field ranges, afford spin ground-state values of S = 14 +/- 1 for complex 1 and S = 9 +/- 1 for complexes 2 and 3. Alternating current susceptibility measurements performed on all three complexes in the 1.8-10 K temperature range in a 3.5 G oscillating field at frequencies between 50 and 1000 Hz reveal out-of-phase chi"M signals below approximately 3 K. Single-crystal hysteresis loop and relaxation measurements confirm single-molecule magnetism behavior.

  15. Marine Mo biogeochemistry in the context of dynamically euxinic mid-depth waters: A case study of the lower Cambrian Niutitang shales, South China

    Science.gov (United States)

    Cheng, Meng; Li, Chao; Zhou, Lian; Algeo, Thomas J.; Zhang, Feifei; Romaniello, Stephen; Jin, Cheng-Sheng; Lei, Li-Dan; Feng, Lian-Jun; Jiang, Shao-Yong

    2016-06-01

    Molybdenum (Mo) concentrations and Mo isotopes have been widely used as proxies for local and global redox conditions in early oceans (>520 Ma) that were stratified and characterized by dynamically euxinic mid-depth waters. However, the nature of the Mo cycle and accompanying isotopic fractionations in such oceans remain poorly known. To fill this gap, we conducted an integrated study of Mo isotopes and redox-sensitive trace element (RSTE) abundances in the Lower Cambrian Niutitang Formation at Yangjiaping, South China. This section accumulated on the northern shelf margin of the Nanhua Basin, a failed intracontinental rift basin with a good connection to the open ocean during the early Cambrian. The Niutitang Formation contains a ∼18-m-thick lower black shale member, and a ∼56-m-thick upper gray silty shale member. The lower member (LM) is moderately to strongly enriched in Mo, U and V, and heterogeneous in Mo isotopic composition (δ98Mo = -0.65‰ to +2.14‰), indicative of dominantly euxinic depositional conditions punctuated by ferruginous episodes (as shown by previously reported Fe speciation data). The upper member (UM) shows lesser enrichment of Mo, U and V, higher Mo/U ratios, and intermediate and more uniform Mo-isotopic compositions (δ98Mo = +1.16‰ to +1.71‰), indicative of weakly oxic to anoxic-euxinic depositional conditions. Geochemical profiles suggest that the LM-to-UM transition reflects a shift of the O2/H2S chemocline from the water column to the sediment. Large δ98Mo fluctuations in the LM may record variations of H2S concentrations in the mid-depth euxinic waters. The intermediate and relatively uniform δ98Mo values of the UM are attributed to the effects of a local Fe-Mn particulate shuttle. In light of the observations at Yangjiaping and other contemporaneous sections in the Nanhua Basin, we propose a new marine Mo biogeochemical model for the early Cambrian ocean. In this model, an Fe-Mn reduction zone may have developed above

  16. High removal efficacy of Hg(II) and MeHg(II) ions from aqueous solution by organoalkoxysilane-grafted lignocellulosic waste biomass.

    Science.gov (United States)

    Saman, Norasikin; Johari, Khairiraihanna; Song, Shiow-Tien; Kong, Helen; Cheu, Siew-Chin; Mat, Hanapi

    2017-03-01

    An effective organoalkoxysilanes-grafted lignocellulosic waste biomass (OS-LWB) adsorbent aiming for high removal towards inorganic and organic mercury (Hg(II) and MeHg(II)) ions was prepared. Organoalkoxysilanes (OS) namely mercaptoproyltriethoxylsilane (MPTES), aminopropyltriethoxylsilane (APTES), aminoethylaminopropyltriethoxylsilane (AEPTES), bis(triethoxysilylpropyl) tetrasulfide (BTESPT), methacrylopropyltrimethoxylsilane (MPS) and ureidopropyltriethoxylsilane (URS) were grafted onto the LWB using the same conditions. The MPTES grafted lignocellulosic waste biomass (MPTES-LWB) showed the highest adsorption capacity towards both mercury ions. The adsorption behavior of inorganic and organic mercury ions (Hg(II) and MeHg(II)) in batch adsorption studies shows that it was independent with pH of the solutions and dependent on initial concentration, temperature and contact time. The maximum adsorption capacity of Hg(II) was greater than MeHg(II) which respectively followed the Temkin and Langmuir models. The kinetic data analysis showed that the adsorptions of Hg(II) and MeHg(II) onto MPTES-LWB were respectively controlled by the physical process of film diffusion and the chemical process of physisorption interactions. The overall mechanism of Hg(II) and MeHg(II) adsorption was a combination of diffusion and chemical interaction mechanisms. Regeneration results were very encouraging especially for the Hg(II); this therefore further demonstrated the potential application of organosilane-grafted lignocellulosic waste biomass as low-cost adsorbents for mercury removal process.

  17. MoS2 spaser

    Science.gov (United States)

    Jayasekara, Charith; Premaratne, Malin; Gunapala, Sarath D.; Stockman, Mark I.

    2016-04-01

    We present a comprehensive analysis of a spaser made of a circular shaped highly doped molybdenum disulfide (MoS2) resonator. "Spaser" is an acronym for "surface plasmon amplification by stimulated emission of radiation"-a nanoscale source of surface plasmons generated by stimulated emission in a plasmonic resonator which receives energy nonradiatively. By considering localized surface plasmon modes, operation characteristics of the model are analysed, and tunability of the design is demonstrated. We find the optimum geometric and material parameters of the spaser that provides efficient outputs and carryout a comparative analysis with a similar circular spaser made of graphene. Owing to physical and chemical properties of MoS2 and the active medium, the proposed design delivers efficient outputs in terms of spaser mode energy, operating thresholds, Q-factor, and electric field amplitude. Lower operating thresholds and higher mode energies are notable advantages of the design. Owing to having many superior features to existing similar designs, this MoS2 spaser may be much suited for applications in nanoplasmonic devices.

  18. The Mn site in Mn-doped Ga-As nanowires: an EXAFS study

    OpenAIRE

    d'Acapito, F.; Rovezzi, M.; Boscherini, F; Jabeen, F; Bais, G.; Piccin, M.; Rubini, S.; Martelli, F.

    2012-01-01

    We present an EXAFS study of the Mn atomic environment in Mn-doped GaAs nanowires. Mn doping has been obtained either via the diffusion of the Mn used as seed for the nanowire growth or by providing Mn during the growth of Au-induced wires. As a general finding, we observe that Mn forms chemical bonds with As but is not incorporated in a substitutional site. In Mn-induced GaAs wires, Mn is mostly found bonded to As in a rather disordered environment and with a stretched bond length, reminisce...

  19. Spectroscopic study of the HgMn star HD 49606: the quest for binarity, abundance stratifications and magnetic field

    Science.gov (United States)

    Catanzaro, G.; Giarrusso, M.; Leone, F.; Munari, M.; Scalia, C.; Sparacello, E.; Scuderi, S.

    2016-08-01

    In this paper, we present a multi-instrument analysis of the mercury-manganese star HD 49606. New spectroscopic observations have been obtained by us with Catania Astrophysical Observatory Spectropolarimeter (CAOS@OAC) and High Accuracy Radial Velocity Planet Searcher-North@Telescopio Nazionale Galileo (HARPS-N@TNG). Combining these observations with archive data coming from other instruments, we performed a comprehensive analysis of this star. We highlight the motion around the centre of mass of a binary system of SB1 type, and we calculate the fundamental parameters characterizing its orbit. We also speculate on the nature of the unseen component. From the fit of H β and H γ, we determined the effective temperature and gravity, while from a number of metal lines, we derive the rotational and microturbulent velocities. Regarding chemical composition, we found underabundances of helium, oxygen, magnesium, sulfur and nickel, solar composition for carbon and overabundances for all the other elements. In particular, mercury abundance is derived taking into account an isotopic mixture different from the terrestrial one. As to magnesium, silicon and phosphorus, we found a non-constant abundance with the optical depth, a result currently considered an evidence of stratification. Spectropolarimetric observations have been performed in the attempt to highlight the presence of a magnetic field, but no detection has been found.

  20. Itinerant and localized magnetic moments in ferrimagnetic Mn{sub 2}CoGa thin films identified with x-ray magnetic linear dichroism: experiment and ab initio theory

    Energy Technology Data Exchange (ETDEWEB)

    Meinert, M.; Schmalhorst, J; Klewe, C.; Reiss, G.; Arenholz, E.; Bohnert, T.; Nielsch, K.

    2011-08-08

    Epitaxial thin films of the half-metallic X{sub a}-compound Mn{sub 2}CoGa (Hg{sub 2}CuTi prototype) were prepared by dc magnetron co-sputtering with different heat treatments on MgO (001) substrates. High-quality lms with a bulk magnetization of 1.95(5) {mu}{sub }B per unit cell were obtained. The average Mn magnetic moment and the Co moment are parallel, in agreement with theory. The x-ray magnetic circular dichroism spectra agree with calculations based on density functional theory and reveal the antiparallel alignment of the two inequivalent Mn moments. X-ray magnetic linear dichroism allows to distinguish between itinerant and localized Mn moments. It is shown that one of the two Mn moments has localized character, whereas the other Mn moment and the Co moment are itinerant.

  1. The Upside to Hg-DOM Associations for Water Quality: Removal of Hg from Solution Using Coagulaion with Metal-Based Salts

    Science.gov (United States)

    Henneberry, Y.; Kraus, T. E.; Fleck, J.; Krabbenhoft, D. P.; Horwath, W. R.

    2011-12-01

    This study assessed the potential use of metal-based coagulants to remove dissolved mercury (Hg) from natural waters and provides information regarding the importance of Hg associations with the dissolved organic matter (DOM) fraction and metal hydroxides. Previous research indicated coagulants were not effective at removing Hg from solution; however those studies used high concentrations of Hg, which did not reflect naturally occurring concentrations of Hg. Filtered water collected from an agricultural drain in the Sacramento-San Joaquin Delta (Delta) was treated with three industrial-grade coagulants (ferric chloride, ferric sulfate, and polyaluminum chloride) to determine their efficacy in removing both inroganic (IHg) and methylmercury (MeHg) from the water column. The Delta suffers from elevated surface water Hg concentrations and as a result is listed as an imparied water body. Coagulants removed up to 85% of DOM from solution. In the absence of DOM, all three coagulants released IHg into solution, however in the presence of DOM the coagulants removed up to 97% of IHg and 80% of MeHg. Results suggest that the removal of Hg is mediated by DOM-coagulant interactions. There was a preferential association of IHg with the more aromatic, higher molecular weight fraction of DOM but no such relationship was found for MeHg. This study offers new fundamental insights regarding large-scale removal of Hg at environmentally relevant concentrations. Research using isotopically labeled Hg is providing insight into whether coagulation can remove recently added Hg (e.g. atmospheric deposition) from solution and whether once formed, the floc can remove additional Hg from the water column.

  2. Study of atomic structure of liquid Hg-In alloys using ab-initio molecular dynamics

    Energy Technology Data Exchange (ETDEWEB)

    Sharma, Nalini; Ahluwalia, P. K. [Department of Physics, Himachal Pradesh University, Shimla(HP)-171005 (India); Thakur, Anil [Department of Physics, Govt. P. G. College Solan (HP)-173212 (India)

    2015-05-15

    Ab-initio molecular dynamics simulations are performed to study the structural properties of liquid Hg-In alloys. The interatomic interactions are described by ab-initio pseudopotentials given by Troullier and Martins. Five liquid Hg-In mixtures (Hg{sub 10}In{sub 90}, Hg{sub 30}In{sub 70}, Hg{sub 50}In{sub 50}, Hg{sub 70}In{sub 30} and Hg{sub 90}In{sub 10}) at 299K are considered. The radial distribution function g(r) and structure factor S(q) of considered alloys are compared with respective experimental results for liquid Hg (l-Hg) and (l-In). The radial distribution function g(r) shows the presence of short range order in the systems considered. Smooth curves of Bhatia-Thornton partial structure factors factor shows the presence of liquid state in the considered alloys.

  3. MoSi2 oxidation resistance coatings for Mo5Si3/MoSi2 composites

    Institute of Scientific and Technical Information of China (English)

    YAN Jianhui; XU Hongmei; ZHANG Houan; TANG Siwen

    2009-01-01

    In order to improve the oxidation resistance properties of 30 at.% Mo5Si3/MoSi2 composite at high temperature in air, a molybdenum disili-tide coating was prepared on its surface by a molten salt technology. XRD and SEM analysis showed that only tetragonal MoSi2 phase ex-isted in the coating after being siliconized for 5 h at 900℃. The oxidation film formed on the uncoated sample was not dense, so that oxygen diffused easily through it. The volatilization of MoO3 resulted in the oxidation film separating from the substrate. The MoSi2coating was proved to be an effective method to prevent 30 at.% MosSi3/MoSi2 composites from being oxidized at 1200℃. A dense glassy SiO2 film was formed on the MoSi2 coating surface, which acted as a barrier layer for the diffusion of oxygen atoms to the substrate. The 30at.% Mo5Si3/MoSi2 composites with a MoSi2 coating showed much better oxidation resistance at high temperature.

  4. Removal of Hg~0 with sodium chlorite solution and mass transfer reaction kinetics

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    The absorption behavior of Hg0 was studied experimentally by using sodium chlorite solution(NaClO2) as the absorbent in a bubble reactor.Primary influencing factors on removal efficiency of Hg0 such as NaClO2 concentration,pH,reaction temperature and the concentration of Hg0 were investigated.The results indicated that 72.91% of Hg0 removal efficiency could be achieved in acidic NaClO2 solution.The removal mechanism of Hg0 was proposed by analyzing of Hg2+ concentration in ab-sorption solution after reaction and comparing the electrode potentials between NaClO2 species and Hg2+/Hg0.The experimental results of mass transfer-reaction kinetics on oxidation of Hg0 by NaClO2 solution showed that with the increase of NaClO2 concentration and the decrease of pH value,the enhancement factor(E) and ratio of KG(Hg0)/kG(Hg0) increased and the liquid phase mass transfer resistance decreased,which is benefit to the mass transfer adsorption reaction.Although the increase of reaction temperature could improve the enhancement factor(E),but the ratio of KG(Hg0)/kG(Hg0) decreased;as a result,the liquid phase mass transfer resistance increased,therefore,the reaction rate for removal of Hg0 decreased.

  5. 640 X 480 Pace HgCdTe FPA

    Science.gov (United States)

    Kozlowski, Lester J.; Bailey, Robert B.; Cabelli, Scott A.; Cooper, Donald E.; McComas, Gail D.; Vural, Kadri; Tennant, William E.

    1992-12-01

    A hybrid HgCdTe 640 X 480 infrared (IR) focal plane array (FPA) that meets the sensitivity, resolution, and field-of-view requirements of high-performance medium wavelength infrared (MWIR) imaging systems has been developed. The key technology making this large, high sensitivity device producible is the epitaxial growth of HgCdTe on a CdTe-buffered, sapphire substrate (referred to as PACE, for Producible Alternative to CdTe for Epitaxy; PACE-I refers to sapphire). The device offers TV resolution with excellent sensitivity at temperatures below 120 K. Mean NE(Delta) T as low as 13 mK has been achieved at operating temperatures nonuniformity compensation.

  6. Electrical Conductivity of HgTe at High Temperatures

    Science.gov (United States)

    Li, C.; Lehoczky, S. L.; Su, C.-H.; Scripa, R. N.

    2004-01-01

    The electrical conductivity of HgTe was measured using a rotating magnetic field method from 300 K to the melting point (943 K). A microscopic theory for electrical conduction was used to calculate the expected temperature dependence of the HgTe conductivity. A comparison between the measured and calculated conductivities was used to obtain the estimates of the temperature dependence of Gamma(sub 6)-Gamma(sub 8) energy gap from 300 K to 943 K. The estimated temperature coefficient for the energy gap was comparable to the previous results at lower temperatures (less than or equal to 300 K). A rapid increase in the conductivity just above 300 K and a subsequent decrease at 500 K is attributed to band crossover effects. This paper describes the experimental approach and some of the theoretical calculation details.

  7. Electronic structure of rectangular HgTe quantum dots

    Science.gov (United States)

    Li, Jian; Zhang, Dong; Zhu, Jia-Ji

    2017-09-01

    We theoretically investigate the single- and few-electron ground-states properties of HgTe topological insulator quantum dots with rectangular hard-wall confining potential using configuration interaction method. For the case of single electron, the edge states is robust against the deformation from a square quantum dot to a rectangular ones, in contrast to the bulk states, the energy gap of the QDs increased due to the coupling of the opposite edge states; for the case of few electrons, the electrons first fill the edge states in the bulk band gap and the addition energy exhibit universal even-odd oscillation due to the shape-independent two-fold degeneracy of the edge states. The size of this edge shell can be controlled by tuning the dot size, shape or the bulk band gap via lateral or vertical electric gating respectively of the HgTe quantum dot.

  8. Stabilization of a Tetrahedral (Mn(5+)O4) Chromophore in Ternary Barium Oxides as a Strategy toward Development of New Turquoise/Green-Colored Pigments.

    Science.gov (United States)

    Laha, Sourav; Tamilarasan, Subramani; Natarajan, Srinivasan; Gopalakrishnan, Jagannatha

    2016-04-04

    An experimental investigation of the stabilization of the turquoise-colored chromophore Mn(5+)O4 in various oxide hosts, viz., A3(VO4)2 (A = Ba, Sr, Ca), YVO4, and Ba2MO4 (M = Ti, Si), has been carried out. The results reveal that substitution of Mn(5+)O4 occurs in Ba3(VO4)2 forming the entire solid solution series Ba3(V1-xMnxO4)2 (0 concept, we synthesized new turquoise-colored Mn(5+)O4 materials, Ba5(BO3)(MnO4)2Cl and Ba5(BO3)(PO4)(MnO4)Cl, based on the apatite-Ba5(PO4)3Cl-structure.

  9. Hvordan understøttes hg-elevers kompetenceudvikling

    DEFF Research Database (Denmark)

    Svejgaard, Karin Løvenskjold; Hansen, Jens Ager; Karmark, Ole

    Publikationen handler om, hvordan hg-elever arbejder og dermed lærer og udvikler kvalifikationer og kompetencer i de undervisnings- og arbejdsformer, de indgår i. Indholdet er baseret på observationer af elever i klasseundervisning, gruppearbejde eller individuel arbejde i forlængelse af...... klasseundervisning og af elever i projektarbejde. Observationerne er gennemført på tre jyske handelsskoler....

  10. EDTA and urease effects on Hg accumulation by Lepidium sativum.

    Science.gov (United States)

    Smolińska, Beata; Cedzyńska, Krystyna

    2007-11-01

    The phytoextraction process was conducted under laboratory conditions with the use of garden cress plants (Lepidium sativum). The experiment was carried out in a model soil, which was characterized before conducting the process. Inorganic forms of mercury (HgCl(2), HgSO(4), Hg(NO(3))(2)) were used for contamination of the soil. The phytoextraction process was conducted after EDTA application to the soil and after urease application. Also the influence of simultaneous addition of ethylenediaminetetraacetic acid (EDTA) and urease into the soil on phytoextraction process was measured. In all variants of phytoextraction process the total mercury concentrations in roots, stems and leaves of garden cress were determined. The result showed that garden cress accumulated mercury from soil. The overall maximum concentration of mercury in its compounds was found in roots of the plant. In all cases, before addition of urease and EDTA, the translocation process and distribution of mercury in the plant tissues were limited. The addition of urease caused an increase of enzyme activity in the soil and at the same time caused an increase of mercury concentration in plant tissues. Application of EDTA increased solubility of mercury and caused an increase of metal accumulation by plants. After simultaneous addition of EDTA and urease into the soil garden cress accumulated about 20% of total mercury concentration in the soil. Most of mercury compounds were accumulated in leaves and stems of the plants (46.0-56.9% of total mercury concentration in the plant tissues).

  11. Barrier formation at graded HgTe/CdTe heterojunctions

    Science.gov (United States)

    Goren, D.; Asa, G.; Nemirovsky, Y.

    1996-11-01

    Numerical calculations of graded HgTe/CdTe heterojunction (HJ) band diagrams at equilibrium are presented and discussed. The calculations are performed in the entire compositional range (0HJs are examined as a function of the graded region width and the graded region doping profiles. The graded region width and doping profiles were found to be the two main factors that determine whether barriers are formed as well as their shape and magnitude. The calculated results indicate that epitaxial ohmic HgTe contacts to extrinsic CdTe are possible, provided that the graded region is wider than one micron, and that it has the same doping type as the doping of the substrate with equal or higher absolute value. Further numerical calculations take into consideration the possible existence of distributed interface charges in the graded region of the HJ. It is shown that by assuming a classical transport over the potential barrier, the effective graded interface charge can be determined from the zero bias differential resistance of the HJ. Experimental transport measurements of metalorganic chemical vapor deposition (MOCVD) grown HgTe/p-CdTe graded HJs show a varying degree of rectification, indicating variations in the graded interface charge distributions which result from different MOCVD growth conditions.

  12. New high-pressure phases of MoSe2 and MoTe2

    Science.gov (United States)

    Kohulák, Oto; MartoÅák, Roman

    2017-02-01

    Three Mo-based transition-metal dichalcogenides MoS2,MoSe2, and MoTe2 share at ambient conditions the same structure 2 Hc , consisting of layers where Mo atoms are surrounded by six chalcogen atoms in trigonal prism coordination. The knowledge of their high-pressure behavior is, however, limited, particularly in case of MoSe2 and MoTe2. The latter materials do not undergo a layer-sliding transition 2 Hc→ 2 Ha known in MoS2 and currently no other stable phase aside from 2 Hc is known in these systems at room temperature. Employing evolutionary crystal structure prediction in combination with ab initio calculations, we study the zero-temperature phase diagram of both materials up to Mbar pressures. We find a tetragonal phase with space group P4/mmm, previously predicted in MoS2, to become stable in MoSe2 at 118 GPa. In MoTe2, we predict at 50 GPa a transition to a new layered tetragonal structure with space group I4/mmm, similar to CaC2, where Mo atoms are surrounded by eight Te atoms. The phase is metallic already at the transition pressure and becomes a good metal beyond 1 Mbar. We discuss chemical trends in the family of Mo-based transition-metal dichalcogenides and suggest that MoTe2 likely offers the easiest route towards the post-2 H phases.

  13. Effect of calcination temperature on structural properties and photocatalytic activity of Mn-C-codoped TiO{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Cai, Jianbo; Xin, Wei; Liu, Guanglong; Lin, Die; Zhu, Duanwei, E-mail: liugl@mail.hzau.edu.cn [Laboratory of Eco-Environmental Engineering Research, College of Resources and Environment, Huazhong Agricultural University (HZAU), Wuhan (China)

    2016-03-15

    Mn-C-codoped TiO{sub 2} catalysts were synthesized by modified sol-gel method based on the self-assembly technique using polyoxyethylene sorbitan monooleate (Tween 80) as template and carbon precursor and the effect of calcination temperature on their structural properties and photocatalytic activity were investigated. The XRD results showed undoped and Mn-C-codoped TiO{sub 2} calcined at 400 deg C only include anatase phase and the rutile phase appears when the calcination temperature reached to 600 deg C. UV-vis absorption spectroscopy demonstrates that the absorption spectra are strongly modified by the calcination temperature. Moreover, the Mn-C-TiO{sub 2} calcined at 400 deg C showed the lowest PL intensity due to a decrease in the recombination rate of photogenerated electrons and holes under light irradiation. The photocatalytic activity of Mn-C-codoped TiO{sub 2} were evaluated by the degradation of methyl orange (MO) under the simulate daylight irradiation and all the prepared Mn-C-codoped TiO{sub 2} samples exhibited high photocatalytic activities for photocatalytic decolorisation of methyl orange aqueous solution. At 400 deg C, the Mn-C-codoped TiO{sub 2} samples showed the highest photocatalytic activity due to synergetic effects of good crystallize ation, appropriate phase composition and slower recombination rate of photogenerated charge carriers, which further confirms the calcination temperature could affect the properties of Mn-C-codoped TiO2 significantly. (author)

  14. Sr<mn>2mn>Ir>1mn><mo>-mo>xRhxO<mn>4mn>(>x<mo><><mn>0.5mn>)> : An inhomogeneous jeff<mo>=>1mn>>2mn> Hubbard system

    Energy Technology Data Exchange (ETDEWEB)

    Chikara, Shalinee; Haskel, Daniel; Sim, Jae-Hoon; Kim, Heung-Sik; Chen, Cheng-Chien; Fabbris, G.; Veiga, L. S. I.; Souza-Neto, N. M.; Terzic, J.; Butrouna, K.; Cao, G.; Han, Myung Joon; van Veenendaal, Michel

    2015-08-24

    In a combined experimental and theoretical study, we investigate the properties of Sr 2 Ir 1 - x Rh x O 4 . From the branching ratios of the L -edge isotropic x-ray absorption spectra, we determine that the spin-orbit coupling is remarkably independent of x for both iridium and rhodium sites. DFT + U calculations show that the doping is close to isoelectronic and introduces impurity bands of predominantly rhodium character close to the lower Hubbard band. Overlap of these two bands leads to metallic behavior. Since the low-energy states for x < 0.5 have predominantly j eff = 1 /2 character, we suggest that the electronic properties of this material can be described by an inhomogeneous Hubbard model, where the on-site energies change due to local variations in the spin-orbit interaction strength combined with additional changes in binding energy.

  15. Formation of Fe-Si-Mn oxyhydroxides at the PACMANUS hydrothermal field, Eastern Manus Basin: Mineralogical and geochemical evidence

    Science.gov (United States)

    Zeng, Zhigang; Ouyang, Hegen; Yin, Xuebo; Chen, Shuai; Wang, Xiaoyuan; Wu, Li

    2012-10-01

    Samples of Fe-Si-Mn oxyhydroxides were collected from the PACMANUS hydrothermal field, which lies in a young back-arc setting in the Eastern Manus Basin. The purpose of the study was to understand the origin and characteristics of Fe-Si-Mn oxyhydroxides associated with massive sulfides in a back-arc basin. The PACMANUS Fe-Si-Mn oxyhydroxides are composed of Fe oxyhydroxides and Mn oxyhydroxides with opal-A and nontronite; they have very low concentrations of trace elements (except for Ba, Mo, V and U) and rare earth elements, and they show REE distribution patterns with positive Eu anomalies and slight enrichments of LREEs. The Fe-Si-Mn oxyhydroxides appear to be precipitated mainly from hydrothermal fluid with limited seawater contamination, and scavenged trace metals are predominantly from the ambient seawater. The differences in the REE distribution patterns between the Fe-oxyhydroxide fraction and Mn-oxyhydroxide fraction originate from diagenetic processes. There are diverse filamentous microtextures resembling unique microbial populations, suggesting microbially-mediated mineralization during the precipitation of the Fe-Si-Mn oxyhydroxides. A possible genetic scenario for the formation of Fe-Si-Mn oxyhydroxides in the PACMANUS hydrothermal field is proposed: (1) precipitation of silica by the mixing of hydrothermal fluid with seawater at a diffuse vent, promoted by Fe-oxidizing bacteria and microbial mineralization; (2) rapid precipitation of Fe-oxyhydroxide from the hydrothermal fluid due to Fe2+ oxidation; (3) growth of Mn-oxyhydroxide partially encasing Fe-oxyhydroxide. Microbes act through the whole scenario. The Fe-Si-Mn oxyhydroxides have undergone changes as a consequence of fluctuating hydrothermal conditions and subsequent diagenetic degradation.

  16. Effect of (Li, Mn) co-doping on structural, optical and magnetic properties of chunk-shaped nano ZnO

    Energy Technology Data Exchange (ETDEWEB)

    Rajamanickam, N., E-mail: nrajamku@gmail.com; Mariammal, R.N.; Rajashabala, S.; Ramachandran, K.

    2014-11-25

    Highlights: • Chunk-shaped nano ZnO synthesized by varying Li and Mn doping concentrations. • The growth mechanism was discussed for chunk-shaped morphologies. • Undoped and Li doped CSNS ZnO exhibit weak ferromagnetic behavior with diamagnetism. • Room temperature ferromagnetism observed for Mn doped and Li/Mn co-doped CSNS ZnO. • Verdet constants and magneto-optic properties were measured from Faraday Effect method. - Abstract: Chunk shaped ZnO nanostructures (CSNS) simultaneously doped with Li and Mn for varying Li/Mn concentrations have been synthesized using wet-chemical method. Their crystal structural, optical and magnetic properties at room temperature (RT) were then investigated, which revealed that all the samples have a single phase with the wurtzite structure. Undoped and co-doped ZnO chunk-shape structures has been demonstrated by transmission electron microscope (TEM). The Mn/Li incorporation also creates more lattice defects and disorders, which influence directly characteristic photoluminescence (PL), FTIR and UV–vis spectra of Zn{sub 1−x−y}Mn{sub y}Li{sub x}O CSNS. Where green emission due to concentration of defects is seen. Magnetic measurements by VSM and the ferro fluid of synthesized nano ZnO by Faraday optical rotation for various concentration of Mn and Li in nano ZnO are done. Change of magnetic and magneto-optic (MO) properties due to Mn and Li ions are discussed in detail.

  17. Manganese (Mn) Oxidation Increases Intracellular Mn in Pseudomonas putida GB-1

    Science.gov (United States)

    Banh, Andy; Chavez, Valarie; Doi, Julia; Nguyen, Allison; Hernandez, Sophia; Ha, Vu; Jimenez, Peter; Espinoza, Fernanda; Johnson, Hope A.

    2013-01-01

    Bacterial manganese (Mn) oxidation plays an important role in the global biogeochemical cycling of Mn and other compounds, and the diversity and prevalence of Mn oxidizers have been well established. Despite many hypotheses of why these bacteria may oxidize Mn, the physiological reasons remain elusive. Intracellular Mn levels were determined for Pseudomonas putida GB-1 grown in the presence or absence of Mn by inductively coupled plasma mass spectrometry (ICP-MS). Mn oxidizing wild type P. putida GB-1 had higher intracellular Mn than non Mn oxidizing mutants grown under the same conditions. P. putida GB-1 had a 5 fold increase in intracellular Mn compared to the non Mn oxidizing mutant P. putida GB-1-007 and a 59 fold increase in intracellular Mn compared to P. putida GB-1 ∆2665 ∆2447. The intracellular Mn is primarily associated with the less than 3 kDa fraction, suggesting it is not bound to protein. Protein oxidation levels in Mn oxidizing and non oxidizing cultures were relatively similar, yet Mn oxidation did increase survival of P. putida GB-1 when oxidatively stressed. This study is the first to link Mn oxidation to Mn homeostasis and oxidative stress protection. PMID:24147089

  18. Phase diagrams and microscopic structures of (Hg,Cd)Te, (Hg,Zn)Te, and (Cd,Zn)Te alloys

    Science.gov (United States)

    Patrick, R. S.; Chen, A.-B.; Sher, A.; Berding, M. A.

    1988-01-01

    A cluster theory based on the quasi-chemical approximation has been applied to study the local correlation bond-length distribution, and phase diagrams of the II-VI pseudobinary alloys Hg(1 - x)Cd(x)Te, Hg(1 - x)Zn(x)Te, and Cd(1 - x)Zn(x)Te. The cluster energy is calculated by letting it relax in some effective alloy medium and then considering the contributions from the strain and chemical energies. Two different models are presented to simulate the alloy medium. While both models show that all three alloys have nearly random distributions, the signs of the local correlation prove to be sensitive to the alloy medium chosen for the energy calculation. Good agreement is found between experiment and the bond lengths and phase diagrams in both models.

  19. Selective Hg(II) adsorption from aqueous solutions of Hg(II) and Pb(II) by hydrolyzed acrylamide-grafted PET films.

    Science.gov (United States)

    Rahman, Nazia; Sato, Nobuhiro; Sugiyama, Masaaki; Hidaka, Yoshiki; Okabe, Hirotaka; Hara, Kazuhiro

    2014-01-01

    Selective Hg(II) adsorption from aqueous solutions of Hg(II) and Pb(II) using hydrolyzed acrylamide (AAm)-grafted polyethylene terephthalate (PET) films was examined to explore the potential reuse of waste PET materials. Selective recovery of Hg(II) from a mixture of soft acids with similar structure, such as Hg(II) and Pb(II), is important to allow the reuse of recovered Hg(II). An adsorbent for selective Hg(II) adsorption was prepared by γ-ray-induced grafting of AAm onto PET films followed by partial hydrolysis through KOH treatment. The adsorption capacity of the AAm-grafted PET films for Hg(II) ions increased from 15 to 70 mg/g after partial hydrolysis because of the reduction of hydrogen bonding between -CONH2 groups and the corresponding improved access of metal ions to the amide groups. The prepared adsorbent was characterized by Fourier transform infrared spectroscopy and scanning electron microscopy. The absorbent film showed high selectivity for the adsorption of Hg(II) over Pb(II) throughout the entire initial metal concentration range (100-500 mg/L) and pH range (2.2-5.6) studied. The high selectivity is attributed to the ability of Hg(II) ions to form covalent bonds with the amide groups. The calculated selectivity coefficient for the adsorbent binding Hg(II) over Pb(II) was 19.2 at pH 4.5 with an initial metal concentration of 100 mg/L. Selective Hg(II) adsorption equilibrium data followed the Langmuir model and kinetic data were well fitted by a pseudo-second-order equation. The adsorbed Hg(II) and Pb(II) ions were effectively desorbed from the adsorbent film by acid treatment, and the regenerated film showed no marked loss of adsorption capacity upon reuse for selective Hg(II) adsorption.

  20. Enhanced Hg{sup 2+} removal and Hg{sup 0} re-emission control from wet fuel gas desulfurization liquors with additives

    Energy Technology Data Exchange (ETDEWEB)

    Tingmei Tang; Jiang Xu; Rongjie Lu; Jingjing Wo; Xinhua Xu [Zhejiang University, Hangzhou (China). Department of Environmental Engineering

    2010-12-15

    Secondary atmospheric pollutions may result from wet flue gas desulfurization (FGD) systems caused by the reduction of Hg{sup 2+} to Hg{sup 0}. The present study employed three agents: Na{sub 2}S, 2,4,6-trimercaptotiazine, trisodium salt nonahydrate (TMT) and sodium dithiocarbamate (DTCR) to precipitate aqueous Hg{sup 2+} in simulated desulfurization solutions. The effects of the precipitator's dosing quantity, the initial pH value, the reaction temperature, the concentrations of Cl{sup -} and other metal ions (e.g. Cu{sup 2+} and Pb{sup 2+}) on Hg{sup 2+} removal were studied. A linear relationship was observed between Hg{sup 2+} removal efficiency and the increasing precipitator's doses along with initial pH. The addition of chloride and metal ions impaired the Hg{sup 2+} removal from solutions due to the complexation of Cl{sup -} and Hg{sup 2+} as well as the chelating competition between Hg{sup 2+} and other metal ions. Based on a comprehensive comparison of the treatment effects, DTCR was found to be the most effective precipitating agent. Moreover, all the precipitating agents were potent enough to inhibit Hg{sup 2+} reduction as well as Hg{sup 0} re-emission from FGD liquors. More than 90% Hg{sup 2+} was captured by precipitating agents while Hg{sup 2+} reduction efficiency decreased from 54% to just less than 3%. The additives could efficiently control the secondary Hg{sup 0} pollution from FGD liquors. 21 refs., 6 figs.

  1. Synthesis and Electrochemical Properties of Semicrystalline Gyroidal Mesoporous MnO2

    Institute of Scientific and Technical Information of China (English)

    ZHOU, Qin; LI, Xiang; LI, Yan-Guang; TIAN, Bo-Zhi; ZHAO, Dong-Yuan; JIANG, Zhi-Yu

    2006-01-01

    Mesoporous silica KIT-6 has novel three-dimensional gyroidal channel structure, space group of Ia-3d, and ordered tunable pores up to 10 nm. In this paper, such mesostructured silica was employed as hard template to prepare semicrystalline gyroidal mesoporous MnO2. The structure was investigated by XRD, TEM and HRTEM, and found to be of high quality Ia-3d symmetry, in good accordance with the template structure. The material has a BET surface of 118 m2·g-1 and pore volume of 0.35 cm3·g-1 after eliminating template. Mesoporous MnO2 has shown good electrochemical property as supercapacitor material in 1 mol·L-1 Na2SO4 and 1 mol·L-1 LiClO4 solutions, but interesting pseudocapacitance behavior was observed in the case of 6 mol·L-1 KOH. It was found that mesoporous MnO2 performed stable reversible electrochemical behavior with capacitance of 220 F·g-1 in a potential range of -0.1-0.55 V vs. Hg/HgO in alkaline solution, demonstrating that it is a promising novel electrode material for the fabrication of electrochemical capacitors.

  2. Characterization of HgCdTe and HgCdSe Materials for Third Generation Infrared Detectors

    Science.gov (United States)

    2011-12-01

    etched HgCdTe photodiode .................................. 13 1.6 (a) Hybrid IR FPA, (b) cross section of structure, (c) indium bumps on Si...to areas of approximately 30 cm2. At this size, the wafers used for growth are unable to accommodate more than two 1024 × 1024 FPAs.3 For more...clear advantages over the other substrates because of its low cost, large wafer size, and a thermal-expansion coefficient that perfectly matches

  3. Maternal-fetal distribution of mercury ( sup 203 Hg) released from dental amalgam fillings

    Energy Technology Data Exchange (ETDEWEB)

    Vimy, M.J.; Takahashi, Y.; Lorscheider, F.L. (Univ. of Calgary, Alberta (Canada))

    1990-04-01

    In humans, the continuous release of Hg vapor from dental amalgam tooth restorations is markedly increased for prolonged periods after chewing. The present study establishes a time-course distribution for amalgam Hg in body tissues of adult and fetal sheep. Under general anesthesia, five pregnant ewes had twelve occlusal amalgam fillings containing radioactive 203Hg placed in teeth at 112 days gestation. Blood, amniotic fluid, feces, and urine specimens were collected at 1- to 3-day intervals for 16 days. From days 16-140 after amalgam placement (16-41 days for fetal lambs), tissue specimens were analyzed for radioactivity, and total Hg concentrations were calculated. Results demonstrate that Hg from dental amalgam will appear in maternal and fetal blood and amniotic fluid within 2 days after placement of amalgam tooth restorations. Excretion of some of this Hg will also commence within 2 days. All tissues examined displayed Hg accumulation. Highest concentrations of Hg from amalgam in the adult occurred in kidney and liver, whereas in the fetus the highest amalgam Hg concentrations appeared in liver and pituitary gland. The placenta progressively concentrated Hg as gestation advanced to term, and milk concentration of amalgam Hg postpartum provides a potential source of Hg exposure to the newborn. It is concluded that accumulation of amalgam Hg progresses in maternal and fetal tissues to a steady state with advancing gestation and is maintained. Dental amalgam usage as a tooth restorative material in pregnant women and children should be reconsidered.

  4. Magnetic anisotropy of [Mo(CN)7]4- anions and fragments of cyano-bridged magnetic networks.

    Science.gov (United States)

    Chibotaru, Liviu F; Hendrickx, Marc F A; Clima, Sergiu; Larionova, Joulia; Ceulemans, Arnout

    2005-08-18

    Quantum chemistry calculations of CASSCF/CASPT2 level together with ligand field analysis are used for the investigation of magnetic anisotropy of [Mo(CN)7]4- complexes. We have considered three types of heptacyano environments: two ideal geometries, a pentagonal bipyramid and a capped trigonal prism, and the heptacyanomolybdate fragment of the cyano-bridged magnetic network K2[Mn(H2O)2]3[Mo(CN)7]2.6H2O. At all geometries the first excited Kramers doublet is found remarkably close to the ground one due to a small orbital energy gap in the ligand field spectrum, which ranges between a maximal value in the capped trigonal prism (800 cm(-1)) and zero in the pentagonal bipyramid. The small value of this gap explains (i) the axial form of the g tensor and (ii) the strong magnetic anisotropy even in strongly distorted complexes. Comparison with available experimental data for the g tensor of the mononuclear precursors reveals good agreement with the present calculations for the capped trigonal prismatic complex and a significant discrepancy for the pentagonal bipyramidal one. The calculations for the heptacyanomolybdate fragment of K2[Mn(H2O)2]3[Mo(CN)7]2.6H2O give g(perpendicular)/g(parallel) approximately 0.5 and the orientation of the local anisotropy axis close to the symmetry axis of an idealized pentagonal bipyramid. These findings are expected to be important for the understanding of the magnetism of anisotropic Mo(III)-Mn(II) cyano-bridged networks based on the [Mo(CN)7]4- building block.

  5. Room-temperature ferromagnetism in Mn-doped CuCrO2 nanopowders

    Directory of Open Access Journals (Sweden)

    DENG Linyan

    2015-08-01

    Full Text Available (Cu1-xMnxCrO2 (0≤x≤6 at% and Cu(Cr1-yMnyO2 (0≤y≤6 at% nanopowders were prepared by combining solid-state reaction and ball milling.It is found that all the samples have a pure 3R-CuCrO2 delafossite structure.The lattice expansion supports the Mn entrance into the Cu and Cr sublattices,respectively,in (Cu1-xMnxCrO2 and Cu(Cr1-yMnyO2,which is further proved by X-ray photoelectron spectroscopy to some degree.Room-temperature ferromagnetism is achieved in B-site Mn-doped samples,originating from the hole-mediated Cr3+-Mn3+ double-exchange interaction.The saturation magnetization of this CuMO2 delafossite (M=Cr,Mn is about an order of magnitude higher than literature values,and gradually decreases with the Mn addition due to the combined influence of the number of the M-M pairs,the M-M distances and the hole density.

  6. Reactivity Descriptors for the Activity of Molecular MN4 Catalysts for the Oxygen Reduction Reaction.

    Science.gov (United States)

    Zagal, José H; Koper, Marc T M

    2016-11-14

    Similarities are established between well-known reactivity descriptors of metal electrodes for their activity in the oxygen reduction reaction (ORR) and the reactivity of molecular catalysts, in particular macrocyclic MN4 metal complexes confined to electrode surfaces. We show that there is a correlation between the M(III) /M(II) redox potential of MN4 chelates and the M-O2 binding energies. Specifically, the binding energy of O2 (and other O species) follows the M(III) -OH/M(II) redox transition for MnN4 and FeN4 chelates. The ORR volcano plot for MN4 catalysts is similar to that for metal catalysts: catalysts on the weak binding side (mostly CoN4 chelates) yield mainly H2 O2 as the product, with an ORR onset potential independent of the pH value on the NHE scale (and therefore pH-dependent on the RHE scale); catalysts on the stronger binding side yield H2 O as the product with the expected pH-dependence on the NHE scale. The suggested descriptors also apply to heat-treated pyrolyzed MN4 catalysts. © 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  7. Characterization of TiC-FeCrMn Cermets Produced by Powder Metallurgy Method

    Directory of Open Access Journals (Sweden)

    Märt Kolnes

    2015-09-01

    Full Text Available TiC-NiMo cermets combine relatively low density with high hardness. Because nickel is known as a toxin and allergen and allergy to nickel is a phenomenon which has assumed growing importance in recent years there has been a flurry of activity to find alternatives to the nickel binder in cermets. It is also the global research and technical development trend in the powder metallurgy cermets industry. In present research TiC-based cermets with FeCrMn binder system were fabricated. Three different sintering conditions were used (vacuum sintering, sinter/HIP and sintering under low Ar pressure. Because of high vapor pressure of manganese different sintering conditions and technologies were investigated to depress the Mn-loss during sintering. Chemical composition of TiC-FeCrMn cermets after different sintering conditions were analyzed by energy-dispersive X-ray spectroscopy (EDS and mechanical properties – hardness and fracture toughness were evaluated on the samples. Results of research showed that Ni-free TiC-based CrMn-steels bonded cermets compare unfavorably with cermets bonded with CrNi austenitic steels in terms of fracture toughness and corrosion resistance. Noticeable Mn-loss during vacuum sintering can be avoided when sintering under low Ar gas pressure.DOI: http://dx.doi.org/10.5755/j01.ms.21.3.7364

  8. MnS clusters in natural zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Iacomi, Felicia; Vasile, Aurelia; Polychroniadis, E.K

    2003-08-15

    FTIR, ESR, optical absorption, photoconductivity, and luminescence measurements are used to evidence the nature of MnS clusters, synthesized by treating the Mn{sup 2+} forms of natural zeolites with Na{sub 2}S.

  9. Electron scattering from 92Mo

    Science.gov (United States)

    Milliman, T. E.; Connelly, J. P.; Heisenberg, J. H.; Hersman, F. W.; Wise, J. E.; Papanicolas, C. N.

    1990-06-01

    Differential cross sections for electron scattering from 92Mo have been measured for excitation energies less than 5.1 MeV over a range of momentum transfer of 0.5 to 3.1 fm-1. The elastic scattering data are analyzed along with existing electron and muonic atom data to provide an improved description of the ground-state charge distribution. The inelastic scattering data have been analyzed to extract electromagnetic transition densities. These densities are interpreted in terms of the underlying nuclear structure.

  10. Olympus Turbo MO 640SII

    Institute of Scientific and Technical Information of China (English)

    蔡翰林

    2001-01-01

    @@ 此款由Olympus推出的TurboMO 640 SII,外观上,以全机身乳白色的优美色调,配合简洁的控制面板;规格上,可读取最大达640MB容量的磁盘片并可向下兼容.在众多的硬件中又多了一台美观实用的MO光盘机可供使用者选择.

  11. Manila clams from Hg polluted sediments of Marano and Grado lagoons (Italy) harbor detoxifying Hg resistant bacteria in soft tissues

    Energy Technology Data Exchange (ETDEWEB)

    Baldi, Franco, E-mail: baldi@unive.it [Dipartimento di Scienze Molecolari e Nanosistemi, Cà Foscari University of Venice, Dorsoduro 2137, 30123 Venice (Italy); Gallo, Michele; Marchetto, Davide [Dipartimento di Scienze Molecolari e Nanosistemi, Cà Foscari University of Venice, Dorsoduro 2137, 30123 Venice (Italy); Faleri, Claudia [Department of Environmental Science ‘G. Sarfatti’, University of Siena, 53100 Siena (Italy); Maida, Isabel; Fani, Renato [Dipartimento di Biologia Evoluzionistica, Via Romana, 17, University of Florence, 50125 Florence (Italy)

    2013-08-15

    A mechanism of mercury detoxification has been suggested by a previous study on Hg bioaccumulation in Manila clams (Ruditapes philippinarum) in the polluted Marano and Grado lagoons and in this study we demonstrate that this event could be partly related to the detoxifying activities of Hg-resistant bacteria (MRB) harbored in clam soft tissues. Therefore, natural clams were collected in six stations during two different periods (winter and spring) from Marano and Grado Lagoons. Siphons, gills and hepatopancreas from acclimatized clams were sterile dissected to isolate MRB. These anatomical parts were glass homogenized or used for whole, and they were lying on a solid medium containing 5 mg l{sup −1} HgCl{sub 2} and incubated at 30 °C. A total of fourteen bacterial strains were isolated and were identified by 16S rDNA sequencing and analysis, revealing that strains were representative of eight bacterial genera, four of which were Gram-positive (Enterococcus, Bacillus, Jeotgalicoccus and Staphylococcus) and other four were Gram-negative (Stenotrophomonas, Vibrio, Raoultella and Enterobacter). Plasmids and merA genes were found and their sequences determined. Fluorescence in situ hybridization (FISH) technique shows the presence of Firmicutes, Actinobacteria and Gammaproteobacteria by using different molecular probes in siphon and gills. Bacterial clumps inside clam flesh were observed and even a Gram-negative endosymbiont was disclosed by transmission electronic microscope inside clam cells. Bacteria harbored in cavities of soft tissue have mercury detoxifying activity. This feature was confirmed by the determination of mercuric reductase in glass-homogenized siphons and gills. -- Highlights: ► We isolated Gram-positive and Gram-negative Hg resistant strains from soft tissues of Ruditapes philippinarum. ► We identify 14 mercury resistant strains by 16S rRNA gene sequences. ► Bacteria in siphon and gill tissues of clams were observed by TEM and identified

  12. Calix[4]arene supported clusters: a dimer of [Mn(III)Mn(II)] dimers

    DEFF Research Database (Denmark)

    Taylor, Stephanie M; McIntosh, Ruaraidh D; Beavers, Christine M;

    2011-01-01

    Phosphinate ligands allow for the transformation of a calix[4]arene supported [Mn(III)(2)Mn(II)(2)] tetramer cluster motif into an unusual [Mn(III)Mn(II)](2) dimer of dimers; the clusters self-assemble in the crystal to form bi-layer arrays reminiscent of the typical packing of calixarene solvates....

  13. First-principles study on the ferrimagnetic half-metallic Mn{sub 2}FeAs alloy

    Energy Technology Data Exchange (ETDEWEB)

    Qi, Santao [Institute for Applied Physics, University of Science and Technology Beijing, Beijing 100083 (China); Zhang, Chuan-Hui, E-mail: zhangch@ustb.edu.cn [National Center for Materials Service Safety, University of Science and Technology Beijing, Beijing 100083 (China); Chen, Bao; Shen, Jiang [Institute for Applied Physics, University of Science and Technology Beijing, Beijing 100083 (China); Chen, Nanxian [Institute for Applied Physics, University of Science and Technology Beijing, Beijing 100083 (China); Department of Physics, Tsinghua University, Beijing 100084 (China)

    2015-05-15

    Mn-based full-Heusler alloys are kinds of promising candidates for new half-metallic materials. Basing on first principles, the electronic structures and magnetic properties of the Mn{sub 2}FeAs full-Heusler alloy have been investigated in detail. The Hg{sub 2}CuTi-type