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Sample records for metallic fe systems

  1. Formation of bulk metallic glasses in the Fe-M-Y-B (M = transition metal) system

    Energy Technology Data Exchange (ETDEWEB)

    Huang, X.M. [International Center for New-Structured Materials (ICNSM) and Laboratory of New-Structured Materials, Department of Materials Science and Engineering, Zhejiang University, Hangzhou 310027 (China); Chang, C.T. [Institute for Material Research, Tohoku University, Sendai 980-8577 (Japan); Chang, Z.Y.; Wang, X.D.; Cao, Q.P. [International Center for New-Structured Materials (ICNSM) and Laboratory of New-Structured Materials, Department of Materials Science and Engineering, Zhejiang University, Hangzhou 310027 (China); Shen, B.L.; Inoue, A. [Institute for Material Research, Tohoku University, Sendai 980-8577 (Japan); Jiang, J.Z. [International Center for New-Structured Materials (ICNSM) and Laboratory of New-Structured Materials, Department of Materials Science and Engineering, Zhejiang University, Hangzhou 310027 (China)], E-mail: jiangjz@zju.edu.cn

    2008-07-28

    In this work, quaternary Fe{sub 72-x}M{sub x}Y{sub 6}B{sub 22} (M = Ni, Co and Mo) bulk metallic glasses (BMGs) have been developed. It is found that a fully amorphous Fe{sub 68}Mo{sub 4}Y{sub 6}B{sub 22} cylindrical rod with 6.5 mm in diameter can be prepared by copper mold injection. These alloys have a high glass transition temperature of about 900 K with high fracture strengths up to about 3 GPa although they are still brittle. Magnetic measurements reveal that they are ferromagnetic at ambient temperature with low coercive force of about 2 A/m, saturation magnetization of about 0.7 T and effective permeability of about 7000 at 100 kHz. The newly developed Fe-based quaternary alloys exhibit excellent combination properties: superior glass forming ability (GFA), high glass transition temperature, and soft magnetic properties, which could have potential applications in electronic industries. Furthermore, the effect of Mo addition on GFA in the Fe-Y-B BMG system has been discussed compared with those of Ni and Co additions.

  2. Experimental Liquidus Studies of the Pb-Fe-Si-O System in Equilibrium with Metallic Pb

    Science.gov (United States)

    Shevchenko, M.; Jak, E.

    2018-02-01

    Phase equilibria of the Pb-Fe-Si-O system have been investigated at 943 K to 1773 K (670 °C to 1500 °C) for oxide liquid in equilibrium with liquid Pb metal and solid oxide phases: (a) quartz, tridymite, or cristobalite; (b) (fayalite + tridymite) or (fayalite + spinel); (c) spinel (Fe3O4); (d) complex lead-iron silicates (melanotekite PbO·FeO1.5·SiO2, barysilite 8PbO·FeO·6SiO2, 5PbO·FeO1.5·SiO2, and 6PbO·FeO1.5·SiO2); (e) lead silicates (Pb2SiO4, Pb11Si3O17); (f) lead ferrites (magnetoplumbite Pb1+ x Fe12- x O19- x solid solution range); and (g) lead oxide (PbO, massicot). High-temperature equilibration on primary phase or iridium substrates, followed by quenching and direct measurement of Pb, Fe, and Si concentrations in the phases with the electron probe X-ray microanalysis, has been used to accurately characterize the system in equilibrium with Pb metal. All results are projected onto the PbO-"FeO"-SiO2 plane for presentation purposes. The present study is the first systematic characterization of liquidus over a wide range of compositions in this system in equilibrium with metallic Pb.

  3. Cluster-based bulk metallic glass formation in Fe-Si-B-Nb alloy systems

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, C L; Wang, Q; Li, F W; Li, Y H; Wang, Y M; Dong, C [State Key Laboratory of Materials Modification, Dalian University of Technology (DUT), Dalian 116024 (China); Zhang, W; Inoue, A, E-mail: dong@dlut.edu.c [Institute for Materials Research (IMR), Tohoku University, Katahira 2-1-1, Aoba-Ku, Sendai 980-8577 (Japan)

    2009-01-01

    Bulk metallic glass formations have been explored in Fe-B-Si-Nb alloy system using the so-called atomic cluster line approach in combination with minor alloying guideline. The atomic cluster line refers to a straight line linking binary cluster to the third element in a ternary system. The basic ternary compositions in Fe-B-Si system are determined by the inetersection points of two cluster lines, namely Fe-B cluster to Si and Fe-Si cluster to B, and then further alloyed with 3-5 at. % Nb for enhancing glass forming abilities. BMG rods with a diameter of 3 mm are formed under the case of minor Nb alloying the basic intersecting compositions of Fe{sub 8}B{sub 3}-Si with Fe{sub 12}Si-B and Fe{sub 8}B{sub 2}-Si with Fe{sub 9}Si-B. The BMGs also exhibit high Vickers hardness (H{sub v}) of 1130-1164 and high Young's modulous (E) of 170-180 GPa

  4. Atomistic modeling of an impurity element and a metal-impurity system: pure P and Fe-P system

    International Nuclear Information System (INIS)

    Ko, Won-Seok; Lee, Byeong-Joo; Kim, Nack J

    2012-01-01

    An interatomic potential for pure phosphorus, an element that has van der Waals, covalent and metallic bonding character, simultaneously, has been developed for the purpose of application to metal-phosphorus systems. As a simplification, the van der Waals interaction, which is less important in metal-phosphorus systems, was omitted in the parameterization process and potential formulation. On the basis of the second-nearest-neighbor modified embedded-atom method (2NN MEAM) interatomic potential formalism applicable to both covalent and metallic materials, a potential that can describe various fundamental physical properties of a wide range of allotropic or transformed crystalline structures of pure phosphorus could be developed. The potential was then extended to the Fe-P binary system describing various physical properties of intermetallic compounds, bcc and liquid alloys, and also the segregation tendency of phosphorus on grain boundaries of bcc iron, in good agreement with experimental information. The suitability of the present potential and the parameterization process for atomic scale investigations about the effects of various non-metallic impurity elements on metal properties is demonstrated. (paper)

  5. Emissions from a Diesel Engine using Fe-based Fuel Additives and a Sintered Metal Filtration System.

    Science.gov (United States)

    Bugarski, Aleksandar D; Hummer, Jon A; Stachulak, Jozef S; Miller, Arthur; Patts, Larry D; Cauda, Emanuele G

    2016-03-01

    A series of laboratory tests were conducted to assess the effects of Fe-containing fuel additives on aerosols emitted by a diesel engine retrofitted with a sintered metal filter (SMF) system. Emission measurements performed upstream and downstream of the SMF system were compared, for cases when the engine was fueled with neat ultralow sulfur diesel (ULSD) and with ULSD treated with two formulations of additives containing Fe-based catalysts. The effects were assessed for four steady-state engine operating conditions and one transient cycle. The results showed that the SMF system reduced the average total number and surface area concentrations of aerosols by more than 100-fold. The total mass and elemental carbon results confirmed that the SMF system was indeed very effective in the removal of diesel aerosols. When added at the recommended concentrations (30 p.p.m. of iron), the tested additives had minor adverse impacts on the number, surface area, and mass concentrations of filter-out (FOut) aerosols. For one of the test cases, the additives may have contributed to measurable concentrations of engine-out (EOut) nucleation mode aerosols. The additives had only a minor impact on the concentration and size distribution of volatile and semi-volatile FOut aerosols. Metal analysis showed that the introduction of Fe with the additives substantially increased Fe concentration in the EOut, but the SMF system was effective in removal of Fe-containing aerosols. The FOut Fe concentrations for all three tested fuels were found to be much lower than the corresponding EOut Fe concentrations for the case of untreated ULSD fuel. The results support recommendations that these additives should not be used in diesel engines unless they are equipped with exhaust filtration systems. Since the tested SMF system was found to be very efficient in removing Fe introduced by the additives, the use of these additives should not result in a measurable increase in emissions of de novo generated

  6. Quality of Metal Deposited Flux Cored Wire With the System Fe-C-Si-Mn-Cr-Mo-Ni-V-Co

    Science.gov (United States)

    Gusev, Aleksander I.; Kozyrev, Nikolay A.; Osetkovskiy, Ivan V.; Kryukov, Roman E.; Kozyreva, Olga A.

    2017-10-01

    Studied the effect of the introduction of vanadium and cobalt into the charge powder fused wire system Fe-C-Si-Mn-Cr-Ni-Mo-V, used in cladding assemblies and equipment parts and mechanisms operating under abrasive and abrasive shock loads. the cored wires samples were manufactured in the laboratory conditions and using appropriate powder materials and as a carbonfluoride contained material were used the dust from gas purification of aluminum production, with the following components composition, %: Al2O3 = 21-46.23; F = 18-27; Na2O = 8-15; K2O = 0.4-6; CaO = 0.7-2.3; Si2O = 0.5-2.48; Fe2O3 = 2.1-3.27; C = 12.5-30.2; MnO = 0.07-0.9; MgO = 0.06-0.9; S = 0.09-0.19; P = 0.1-0.18. Surfacing was produced on the St3 metal plates in 6 layers under the AN-26C flux by welding truck ASAW-1250. Cutting and preparation of samples for research had been implemented. The chemical composition and the hydrogen content of the weld metal were determined by modern methods. The hardness and abrasion rate of weld metal had been measured. Conducted metallographic studies of weld metal: estimated microstructure, grain size, contamination of oxide non-metallic inclusions. Metallographic studies showed that the microstructure of the surfaced layer by cored wire system Fe-C-Si-Mn-Cr-Mo-Ni-V-Co is uniform, thin dendrite branches are observed. The microstructure consists of martensite, which is formed inside the borders of the former austenite grain retained austenite present in small amounts in the form of separate islands, and thin layers of δ-ferrite, which is located on the borders of the former austenite grains. Carried out an assessment the effect of the chemical composition of the deposited metal on the hardness and wear and hydrogen content. In consequence of multivariate correlation analysis, it was determined dependence to the hardness of the deposited layer and the wear resistance of the mass fraction of the elements included in the flux-cored wires of the system Fe

  7. Hybrid materials based on polymethylsilsesquioxanes containing Fe, Pt, and Fe-Pt metallic nanoparticles

    Science.gov (United States)

    Vasil'kov, A. Yu.; Migulin, D. A.; Naumkin, A. V.; Zubavichus, Ya. V.; Budnikov, A. V.; Ellert, O. G.; Maksimov, Yu. V.; Muzafarov, A. M.

    2017-11-01

    New hybrid materials based on Pt, Fe, and Pt-Fe nanoparticles stabilized in a matrix of polymethylsilsesquioxane nanogel and ultrahigh molecular weight polyethylene (UHMWPE) were prepared. Metal vapor synthesis was used to produce mono- and bimetallic nanoparticles. It was shown that organosilicon nanogel effectively stabilizes Pt nanoparticles with an average size of 0.9 nm. Using the nanogel results in the formation of superparamagnetic Fe particles 3-5 nm in size that consist of ferromagnetic Fe0 core and antiferromagnetic shells of Fe oxides. It is established that using an organosilicon matrix in the formation of Pt-Fe/UHMWPE systems helps reduce the average particle size of Fe in the material from 6.5 to 4.5 nm and narrow their particle size distribution. The composition, magnetic and electronic characteristics of the nanocomposites are studied via transmission electron microscopy, X-ray photoelectron spectroscopy, Mössbauer spectroscopy, XANES, and EXAFS.

  8. Half-metallic compensated ferrimagnetism with a tunable compensation point over a wide temperature range in the Mn-Fe-V-Al Heusler system

    Directory of Open Access Journals (Sweden)

    Rolf Stinshoff

    2017-10-01

    Full Text Available The cubic Heusler compound Mn1.5FeV0.5Al with the L21 Heusler structure is the first fully compensated half-metallic ferrimagnet with 24 valence electrons. The ferrimagnetic state can be tuned by changing the composition such that the compensation point appears at finite temperatures ranging from 0 K up to 226 K, while retaining half-metallicity in the system. In this paper, the structural, magnetic and transport properties of the Mn-Fe-V-Al system are discussed. Magnetic reversal and a change of sign of the anomalous Hall effect were observed at the compensation point, which gives rise to a sublattice spin-crossing. These materials present new possibilities for potential spintronic devices because of their advantageous properties such as imperceptibility to external fields, lower power consumption and ultrafast switching in the THz region.

  9. Experimental Phase Equilibria Studies of the Pb-Fe-O System in Air, in Equilibrium with Metallic Lead and at Intermediate Oxygen Potentials

    Science.gov (United States)

    Shevchenko, M.; Jak, E.

    2017-12-01

    The phase equilibria information on the Pb-Fe-O system is of practical importance for the improvement of the existing thermodynamic database of lead-containing slag systems (Pb-Zn-Fe-Cu-Si-Ca-Al-Mg-O). Phase equilibria of the Pb-Fe-O system have been investigated: (a) in air at temperatures between 1053 K and 1373 K (780 °C and 1100 °C); (b) in equilibrium with metallic lead at temperatures between 1053 K and 1373 K (780 °C and 1100 °C); and (c) at intermediate oxidation conditions for the liquid slag in equilibrium with two solids (spinel + magnetoplumbite), at temperatures between 1093 K and 1373 K (820 °C and 1100 °C). The high-temperature equilibration/quenching/electron probe X-ray microanalysis technique has been used to accurately determine the compositions of the phases in equilibrium in the system. The Pb and Fe concentrations in the phases were determined directly; preliminary thermodynamic modeling with FactSage was used to estimate the ferrous-to-ferric ratios and to present the results in the ternary diagram.

  10. Application of Fe-based metallic glasses in wastewater treatment

    International Nuclear Information System (INIS)

    Lin Bao; Bian Xiufang; Wang Pan; Luo Guanping

    2012-01-01

    Highlights: ► We found the Fe-based metallic glasses have potential application in wastewater treatment. ► The corrosion on the surface of Fe-based metallic glasses is related to the application. ► We set a new theory to explain the process of degredation organic metters with Fe-based metallic glasses. - Abstract: This work pioneered the use of the Fe 78 Si 9 B 13 metallic glass ribbons in wastewater treatment. Fe 78 Si 9 B 13 metallic glass was employed to remediate wastewater contaminated with a mixture of organic dyes. The removal rate of chemical oxygen demand (COD) with Fe 78 Si 9 B 13 metallic glass and metallic Fe 0 was up to 23 ± 0.93% in 30 min and 21 ± 0.67% with in 45 min, respectively. The dosage of Fe-based metallic glass was only 1/25 of that of metallic Fe 0 to obtain equivalent effects. The mechanism of wastewater treatment through Fe-based metallic glasses is discussed.

  11. Thermodynamic assessment of the La-Fe-O system

    DEFF Research Database (Denmark)

    Povoden-Karadeniz, E.; Grundy, A.N.; Chen, Ming

    2009-01-01

    The La-Fe and the La-Fe-O systems are assessed using the Calphad approach, and the Gibbs energy functions of ternary oxides are presented. Oxygen and mutual La and Fe solubilities in body-centered cubic (bcc) and face-centered cubic (fcc) structured metallic phases are considered in the modeling....

  12. Novel electrochemical approaches to micro- and nanoscale metallic materials for advanced magnetic and energy applications: Co-In, Fe-Rh and Fe-P systems

    OpenAIRE

    Golvano-Escobal, Irati

    2017-01-01

    Bibliografia La presente tesis doctoral abarca la síntesis electroquímica y caracterización de las propiedades tanto físicas como fisicoquímicas de tres sistemas binarios diferentes, el cobalto-indio (Co-In), hierro-rodio (Fe-Rh) y hierro-fósforo (Fe-P). Se han llevado a cabo varias estrategias para miniaturizar estos sistemas tanto hacia la micro- como hacia la nanoescala. Se han sintetizado capas continuas de Co-In, sobre sustratos conductores de silicio recubiertos con capas semilla de ...

  13. Semiconductor-to-metallic flipping in a ZnFe2O4–graphene based smart nano-system: Temperature/microwave magneto-dielectric spectroscopy

    International Nuclear Information System (INIS)

    Ameer, Shahid; Gul, Iftikhar Hussain; Mahmood, Nasir; Mujahid, Muhammad

    2015-01-01

    Zn-(FeO 2 ) 2 –graphene smart nano-composites were synthesized using a novel modified solvothermal synthesis with different percentages of graphene. The structure of the nanocomposite was confirmed through X-ray diffraction, micro-Raman scattering spectroscopy, Ultraviolet–Visible spectroscopy, and Fourier transform infrared spectroscopy. The structural growth and morphological aspects were analyzed using scanning/transmission electron microscopy, revealing marvelous micro-structural features of the assembled nano-system resembling a maple leaf. To determine the composition, energy dispersive spectroscopy and X-ray photoelectron spectroscopy were used. Microwave magneto-dielectric spectroscopy revealed the improved dielectric properties of the nano-composite compared to those of the parent functional nanocrystals. Temperature gradient dielectric spectroscopy was used over the spectral range from 100 Hz to 5 MHz to reveal the phenomenological effect that the nanosystem flips from its usual semiconductor nature to a metallic nature with sensing temperature. Electrical conductivity and dielectric analysis indicated that the dielectric loss and the dielectric permittivity increased at room temperature. This extraordinary switching capability of the functionalized graphene nanosystem opens up a new dimension for engineering advanced and efficient smart composite materials. - Graphical abstract: Display Omitted - Highlights: • Zn-(FeO 2 ) 2 –graphene smart nano-composites were synthesized using a novel modified solvothermal synthesis. • The synthesized nano-system exhibits marvelous leaf like microstructure. • These nano-composites show improved magneto dielectric response. • This engineered smart nano-system shows phenomenological flipping from semiconductor like nature to metallic behavior

  14. Mechanical alloying of the FeNi-Ag system

    International Nuclear Information System (INIS)

    Gonzalez, G.; Ibarra, D.; Ochoa, J.; Villalba, R.; Sagarzazu, A.

    2007-01-01

    The Fe-Ni-Ag system is of particular interest for its potential applications as soft magnetic granular material with small magnetic grains embedded in a non-magnetic metal matrix. Under equilibrium conditions: Fe-Ag and Ni-Ag are immiscible and Fe-Ni shows complete solubility. These materials are particularly important for magnetoresistivity properties. The properties of these alloys are closely related to their microstructure; therefore, a detailed study of the transformations occurring during milling was undertaken using pre-alloyed Fe x Ni 100-x (x = 30, 50 and 70) further milled with different Ag content to give the following alloys compositions (Fe x -Ni 100-x ) 100-y Ag y (y = 5, 20, 60). Consolidation of the mechanically alloyed powders by sintering at 950 o C was performed. Morphological and structural characterization of the sintered powders was carried out by scanning and transmission electron microscopy and X-ray diffraction. Fe 30 Ni 70 and Fe 50 Ni 50 formed ordered FeNi 3 compound. Fe 70 Ni 30 showed the formation of a mixture of γ-(Fe,Ni) and α-Fe(Ni) solid solutions. The mixture of these systems with Ag showed the metal solid solutions surrounded by Ag islands of Fe x Ni y -Ag, There was also evidence of Ag diffusing into the γ-(Fe,Ni). High Ag content (60%) shows formation of islands of FeNi surrounded by Ag. Sintering is always improved with the Ag content

  15. Accelerated decarburization of Fe-C metal alloys

    Science.gov (United States)

    Pal, Uday B.; Sadoway, Donald R.

    1997-01-01

    A process for improving the rate of metal production and FeO utilization in a steelmaking process or a process combining iron-making and steelmaking in a single reactor that uses or generates Fe-C metal alloy droplets submerged in an FeO-containing slag. The process involves discharging a charge build-up (electron accumulation) in the slag at the slag-metal alloy interface by means of an electron conductor connected between the metal alloy droplets and a gas at a gas-slag interface, said gas having an oxygen partial pressure of at least about 0.01 atmosphere.

  16. Investigating Planetesimal Evolution by Experiments with Fe-Ni Metallic Melts: Light Element Composition Effects on Trace Element Partitioning Behavior

    Science.gov (United States)

    Chabot, N. L.

    2017-12-01

    As planetesimals were heated up in the early Solar System, the formation of Fe-Ni metallic melts was a common occurrence. During planetesimal differentiation, the denser Fe-Ni metallic melts separated from the less dense silicate components, though some meteorites suggest that their parent bodies only experienced partial differentiation. If the Fe-Ni metallic melts did form a central metallic core, the core eventually crystallized to a solid, some of which we sample as iron meteorites. In all of these planetesimal evolution processes, the composition of the Fe-Ni metallic melt influenced the process and the resulting trace element chemical signatures. In particular, the metallic melt's "light element" composition, those elements present in the metallic melt in a significant concentration but with lower atomic masses than Fe, can strongly affect trace element partitioning. Experimental studies have provided critical data to determine the effects of light elements in Fe-Ni metallic melts on trace element partitioning behavior. Here I focus on combining numerous experimental results to identify trace elements that provide unique insight into constraining the light element composition of early Solar System Fe-Ni metallic melts. Experimental studies have been conducted at 1 atm in a variety of Fe-Ni systems to investigate the effects of light elements on trace element partitioning behavior. A frequent experimental examination of the effects of light elements in metallic systems involves producing run products with coexisting solid metal and liquid metal phases. Such solid-metal-liquid-metal experiments have been conducted in the Fe-Ni binary system as well as Fe-Ni systems with S, P, and C. Experiments with O-bearing or Si-bearing Fe-Ni metallic melts do not lend themselves to experiments with coexisting solid metal and liquid metal phases, due to the phase diagrams of these elements, but experiments with two immiscible Fe-Ni metallic melts have provided insight into

  17. Fe-based bulk metallic glasses used for magnetic shielding

    Science.gov (United States)

    Şerban, Va; Codrean, C.; Uţu, D.; Ercuţa, A.

    2009-01-01

    The casting in complex shapes (tubullar) and the main magnetic properties of bulk metallic glasses (BMG) alloys from the ferromagnetic Fe-Cr-Ni-Ga-P-Si-C system, with a small adittion of Ni (3%) were studied. Samples as rods and sockets having the thickness up to 1 mm were obtained from master alloys by melt injection by low cooling rates into a Cu mold and annealed in order to ensure adequate magnetic requirements. The structure was examined by X-ray diffraction (XRD) and the basic magnetic properties (coercivity, magnetic remanence, initial susceptibility, etc.) were determined by conventional low frequency induction method. The experimental investigations on producing of BMG ferromagnetic alloys with 3% Ni show the possibility to obtain magnetic shields of complex shape with satisfactory magnetic properties. The presence of Ni does not affect the glass forming ability, but reduce the shielding capacity.

  18. Fe-based bulk metallic glasses used for magnetic shielding

    Energy Technology Data Exchange (ETDEWEB)

    Serban, Va; Codrean, C; UTu, D [Politehnica University of Timisoara, Depart for Materials Science and Welding, 1, M. Viteazu Bvd., 300222, Timisoara (Romania); ErcuTa, A, E-mail: serban@mec.upt.r [West University of Timisoara, Faculty of Physics, 4, Vasile Parvan Bdv., Timisoara 300223 (Romania)

    2009-01-01

    The casting in complex shapes (tubular) and the main magnetic properties of bulk metallic glasses (BMG) alloys from the ferromagnetic Fe-Cr-Ni-Ga-P-Si-C system, with a small addition of Ni (3%) were studied. Samples as rods and sockets having the thickness up to 1 mm were obtained from master alloys by melt injection by low cooling rates into a Cu mold and annealed in order to ensure adequate magnetic requirements. The structure was examined by X-ray diffraction (XRD) and the basic magnetic properties (coercivity, magnetic remanence, initial susceptibility, etc.) were determined by conventional low frequency induction method. The experimental investigations on producing of BMG ferromagnetic alloys with 3% Ni show the possibility to obtain magnetic shields of complex shape with satisfactory magnetic properties. The presence of Ni does not affect the glass forming ability, but reduce the shielding capacity.

  19. Phase relations in the Fe-Fe3C-Fe3N system at 7.8 GPa and 1350 °C: Implications for carbon and nitrogen hosts in Fe0-saturated upper mantle

    Science.gov (United States)

    Sokol, Alexander G.; Kruk, Alexey N.; Seryotkin, Yurii V.; Korablin, Alexander A.; Palyanov, Yury N.

    2017-04-01

    Phase relations in the Fe-Fe3C-Fe3N system are studied in high-pressure experiments at 7.8 GPa and 1350 °C using a split-sphere multi-anvil apparatus. The starting mixtures consisting of Fe, Fe3C and Fe3N are loaded into ceramic or graphite capsules. Contamination with trace amounts of oxygen leads to the appearance of wüstite in the system retaining oxygen fugacity (fO2) near the iron-wüstite (IW) buffer. The metal melt rich in carbon and nitrogen has a large stability field in the central part of the phase diagram, and this field at 1350 °C is tangent to the Fe-Fe3C side of the Fe-Fe3C-Fe3N triangle at the point of the Fe-Fe3C eutectics. Iron nitride ε-Fe3N (space group P6322 or P63/mmc) contains variable amounts of C and N: up to 2.0-2.5 wt% C and 6.0-7.3 wt% N in equilibrium with a C- and N-rich melt and as little as 1.0 wt% C and 3.2 wt% N in equilibrium with γ- Fe. The limit C and N contents in γ-Fe equilibrated with the C- and N-rich melt is about 1.0 wt%, while the N solubility in cementite (Fe3C) does not exceed 0.5 wt%. The obtained data make basis for the isothermal section of the Fe-Fe3C-Fe3N system. The metal melt phase is inferred to be the main host of carbon and nitrogen in the Fe0-saturated (0.1 wt%) mantle at a depth of ∼250 km. In particular, C- and N-bearing austenite (γ-Fe) and metal melts host carbon and nitrogen in the mantle depleted in volatiles (20 ppm C and 1 ppm N), whereas carbon and nitrogen in the mantle with high concentrations of volatiles (250 ppm C and 100 ppm N) reside in C- and N-rich melts with a minor amount of iron carbide (Fe3C). The presence of nickel and sulphur in metal are expected to inhibit the formation of iron carbide and increases the melt phase stability. Redox freezing of N-rich carbonate melts from subduction slabs in Fe0-saturated mantle may produce iron melts supersaturated with nitrogen and stable ε-Fe3N.

  20. Improved Automotive NO (x) Aftertreatment System: Metal Ammine Complexes as NH3 Source for SCR Using Fe-Containing Zeolite Catalysts

    DEFF Research Database (Denmark)

    Johannessen, Tue; Schmidt, Henning; Frey, Anne Mette

    2009-01-01

    Ammonia storage is a challenge in the selective catalytic reduction of NO (x) in vehicles. We propose a new system, based on metal ammines as the ammonia source. In combination with iron containing zeolites as the SCR catalyst it should be possible to obtain a low temperature system for NO (x...

  1. Phase relations in the metal-rich portions of the phase system Pt-Ir-Fe-S at 1000 degrees C and 1100 degrees C

    DEFF Research Database (Denmark)

    Makovicky, E.; Karup-Møller, Sven

    2000-01-01

    with gamma-(Pt,Fe), Pt3Fe and PtFe which dissolve respectively at least 5.1, 29.3 and 24.0 at.% Ir at 1100 degreesC (2.2, 23.6 and less than or equal to 17.2 at.% Ir at 1000 degreesC). Gaps between the nearly Ir-free Pt-Fe alloys gamma (Pt,Fe), Pt3Fe s.s., PtFe s.s. and gamma (Fe,Pt) were estimated as 20...

  2. Alkali Metal Variation and Twisting of the FeNNFe Core in Bridging Diiron Dinitrogen Complexes.

    Science.gov (United States)

    McWilliams, Sean F; Rodgers, Kenton R; Lukat-Rodgers, Gudrun; Mercado, Brandon Q; Grubel, Katarzyna; Holland, Patrick L

    2016-03-21

    Alkali metal cations can interact with Fe-N2 complexes, potentially enhancing back-bonding or influencing the geometry of the iron atom. These influences are relevant to large-scale N2 reduction by iron, such as in the FeMoco of nitrogenase and the alkali-promoted Haber-Bosch process. However, to our knowledge there have been no systematic studies of a large range of alkali metals regarding their influence on transition metal-dinitrogen complexes. In this work, we varied the alkali metal in [alkali cation]2[LFeNNFeL] complexes (L = bulky β-diketiminate ligand) through the size range from Na(+) to K(+), Rb(+), and Cs(+). The FeNNFe cores have similar Fe-N and N-N distances and N-N stretching frequencies despite the drastic change in alkali metal cation size. The two diketiminates twist relative to one another, with larger dihedral angles accommodating the larger cations. In order to explain why the twisting has so little influence on the core, we performed density functional theory calculations on a simplified LFeNNFeL model, which show that the two metals surprisingly do not compete for back-bonding to the same π* orbital of N2, even when the ligand planes are parallel. This diiron system can tolerate distortion of the ligand planes through compensating orbital energy changes, and thus, a range of ligand orientations can give very similar energies.

  3. Metal transports and enrichments in iron depositions hosted in basaltic rocks. II: Metal rich fluids and Fe origin

    Science.gov (United States)

    Zhang, Ronghua; Zhang, Xuetong; Hu, Shumin

    2015-12-01

    This study focuses on revealing the mechanism of metal transport, enrichment and Fe origin of iron deposition during water basalt interactions occurred in basaltic rocks. Observations of the iron deposits (anhydrite-magnetite-pyroxene type deposits) hosted in K-rich basaltic rocks in the Mesozoic volcanic area of the Middle-Lower Yangtze River valley, China, indicate that the mechanism of metal transport and enrichment for those deposits are significant objective to scientists, and the Fe origin problem is not well resolved. Here the metal transport, enrichment and iron origin have been investigated in high temperature experiments of water basaltic interactions. These deposits were accompanying a wide zone with metal alteration. The effects of hydrothermal alteration on major rock-forming element concentrations in basaltic rock were investigated by systematically comparing the chemical compositions of altered rocks with those of fresh rocks. In the deposits, these metals are distributed throughout altered rocks that exhibit vertical zoning from the deeper to the shallow. Then, combined with the investigations of the metal-alterations, we performed kinetic experiments of water-basaltic rock interactions using flow-through reactors in open systems at temperatures from 20 °C to 550 °C, 23-34 MPa. Release rates for the rock-forming elements from the rocks have been measured. Experiments provide the release rates for various elements at a large temperature range, and indicate that the dissolution rates (release rates) for various elements vary with temperature. Si, Al, and K have high release rates at temperatures from 300 °C to 500 °C; the maximum release rates (RMX) for Si are reached at temperatures from 300 °C to 400 °C. The RMXs for Ca, Mg, and Fe are at low temperatures from 20 °C to 300 °C. Results demonstrate that Fe is not released from 400 °C to 550 °C, and indicate that when deep circling fluids passed through basaltic rocks, Fe was not mobile, and

  4. Metal Injection Molding (MIM) of NdFeB Magnets

    OpenAIRE

    Hartwig T.; Lopes L.; Wendhausen P.; Ünal N.

    2014-01-01

    Due to the increased and unstable prices for Rare Earth elements there are activities to develop alternative hard magnetic materials. Reducing the amount of material necessary to produce complex sintered NdFeB magnets can also help to reduce some of the supply problem. Metal Injection Molding (MIM) is able to produce near net shape parts and can reduce the amount of finishing to achieve final geometry. Although MIM of NdFeB has been patented and published fairly soon after the development of ...

  5. Enhancement of plasticity of Fe-based bulk metallic glass by Ni substitution for Fe

    Energy Technology Data Exchange (ETDEWEB)

    Guo, S.F. [State Key Laboratory of Material Processing and Die and Mould Technology, Huazhong University of Science and Technology, 430074 Wuhan (China); State Key Laboratory for Advanced Metals and Materials, University of Science and Technology Beijing, Beijing 100083 (China); Li, N.; Zhang, C. [State Key Laboratory of Material Processing and Die and Mould Technology, Huazhong University of Science and Technology, 430074 Wuhan (China); Liu, L., E-mail: sfguo2005@163.co [State Key Laboratory of Material Processing and Die and Mould Technology, Huazhong University of Science and Technology, 430074 Wuhan (China)

    2010-08-15

    Bulk metallic glasses (BMGs) (Fe{sub 1-x}Ni{sub x}){sub 71}Mo{sub 5}P{sub 12}C{sub 10}B{sub 2} (x = 0, 0.1 and 0.2) with a diameter of 3 mm were synthesized by copper mold casting. The effect of Ni substitution for Fe on the structure, thermal and mechanical properties has been studied by X-ray diffraction (XRD), differential scanning calorimetry (DSC) and compressive testing. It was found that the substitution of Ni for Fe enhances the glass forming ability, and improves the plasticity of Fe{sub 71}Mo{sub 5}P{sub 12}C{sub 10}B{sub 2} BMG as indicated by the increase in the plastic strain from 3.1% (x = 0) to 5.2% (x = 0.2). The improvement of the plasticity is discussed in term of the reduction of glass transition temperature and the supercooled liquid region due to the substitution of Ni for Fe.

  6. Fabrication and characterization of nanostructured Fe3S4, an isostructural compound of half-metallic Fe3O4

    KAUST Repository

    Li, Peng

    2015-06-10

    High-purity, well-crystallized spinel Fe3S4 nanoplatelets were synthesized by the hydrothermal method, and the saturation magnetic moment of Fe3S4 was measured at 1.83 μB/f.u. The temperature-dependent resistivity of Fe3S4 was metallic-like for T < 180 K: room-temperature resistivity was measured at 7.711 × 103  μΩ cm. The anomalous Hall conductivity of Fe3S4 decreased with increasing longitudinal conductivity, in sharp contrast with the accepted theory of the anomalous Hall effect in a dirty-metal regime. Furthermore, negligible spin-dependent magnetoresistance was observed. Band structure calculations confirmed our experimental observations that Fe3S4 is a metal and not a half metal as expected.

  7. High pressure die casting of Fe-based metallic glass

    Science.gov (United States)

    Ramasamy, Parthiban; Szabo, Attila; Borzel, Stefan; Eckert, Jürgen; Stoica, Mihai; Bárdos, András

    2016-10-01

    Soft ferromagnetic Fe-based bulk metallic glass key-shaped specimens with a maximum and minimum width of 25.4 and 5 mm, respectively, were successfully produced using a high pressure die casting (HPDC) method, The influence of die material, alloy temperature and flow rate on the microstructure, thermal stability and soft ferromagnetic properties has been studied. The results suggest that a steel die in which the molten metal flows at low rate and high temperature can be used to produce completely glassy samples. This can be attributed to the laminar filling of the mold and to a lower heat transfer coefficient, which avoids the skin effect in the steel mold. In addition, magnetic measurements reveal that the amorphous structure of the material is maintained throughout the key-shaped samples. Although it is difficult to control the flow and cooling rate of the molten metal in the corners of the key due to different cross sections, this can be overcome by proper tool geometry. The present results confirm that HPDC is a suitable method for the casting of Fe-based bulk glassy alloys even with complex geometries for a broad range of applications.

  8. High pressure die casting of Fe-based metallic glass.

    Science.gov (United States)

    Ramasamy, Parthiban; Szabo, Attila; Borzel, Stefan; Eckert, Jürgen; Stoica, Mihai; Bárdos, András

    2016-10-11

    Soft ferromagnetic Fe-based bulk metallic glass key-shaped specimens with a maximum and minimum width of 25.4 and 5 mm, respectively, were successfully produced using a high pressure die casting (HPDC) method, The influence of die material, alloy temperature and flow rate on the microstructure, thermal stability and soft ferromagnetic properties has been studied. The results suggest that a steel die in which the molten metal flows at low rate and high temperature can be used to produce completely glassy samples. This can be attributed to the laminar filling of the mold and to a lower heat transfer coefficient, which avoids the skin effect in the steel mold. In addition, magnetic measurements reveal that the amorphous structure of the material is maintained throughout the key-shaped samples. Although it is difficult to control the flow and cooling rate of the molten metal in the corners of the key due to different cross sections, this can be overcome by proper tool geometry. The present results confirm that HPDC is a suitable method for the casting of Fe-based bulk glassy alloys even with complex geometries for a broad range of applications.

  9. New Half-Metallic Materials: FeRuCrP and FeRhCrP Quaternary Heusler Compounds

    Directory of Open Access Journals (Sweden)

    Jiannan Ma

    2017-11-01

    Full Text Available The electronic structures and magnetic properties of FeRuCrP and FeRhCrP quaternary Heusler compounds with LiMgPbSb-type structures have been investigated via first-principles calculations. The calculational results show that both FeRuCrP and FeRhCrP compounds present perfect half-metallic properties: Showing large half-metallic band gaps of 0.39 eV and 0.38 eV, respectively. The total magnetic moments of FeRuCrP and FeRhCrP are 3 μB and 4 μB per formula unit, respectively. The magnetism of them mainly comes from the 3d electrons of Cr atoms and follows the Slater-Paulig behavior of Heusler compounds: Mt = Zt − 24. Furthermore, the half-metallic properties of FeRuCrP and FeRhCrP compounds can be kept in a quite large range of lattice constants (about 5.44–5.82 Å and 5.26–5.86 Å, respectively and are quite robust against tetragonal deformation (c/a ratio in the range of 0.94–1.1 and 0.97–1.1, respectively. Moreover, the large negative cohesion energy and formation energy of FeRuCrP and FeRhCrP compounds indicate that they can be synthesized experimentally.

  10. Integrated hydrogen evolution and water-cleaning via a robust graphene supported noble-metal-free Fe1-xCoxS2system.

    Science.gov (United States)

    Fan, Yingying; Wang, Dandan; Han, Dongxue; Ma, Yingming; Ni, Shuang; Sun, Zhonghui; Dong, Xiandui; Niu, Li

    2017-05-11

    In an electrocatalytic hydrogen evolution reaction (HER) system, a cathodic H + resource, an anodic sacrificial agent and a robust catalyst are three essential factors. Industry wastewater emissions, containing high levels of acidity and organic dyes, actually can satisfy the material requirements for the HER. Herein, a new HER method is proposed, taking acidic ions from wastewater as a cathodic resource to produce H 2 , while organic dye waste acts as an anodic sacrifice to balance the reaction. In such a way, a sustainable H 2 energy source can be generated and clean water is obtained as well. For the HER catalyst, low cost and highly efficient graphene supported Fe 1-x Co x S 2 was synthesized with an onset overpotential of ∼50 mV and it demonstrated impressive HER performance in both practical industry wastewater and analogous wastewater simulations. Besides the cathodic H 2 evolution, anodic organic dyes (MO, MB, RhB and industry waste organic dyes) were all entirely decomposed within 8 min, 18 min, 9 min and 4 h under oxidation potentials of ∼1.46, 1.50, 1.47 and 1.40 V. As verified both in practical industry wastewater and wastewater simulations in the laboratory, our approach for integrating the HER and wastewater treatment puts forward an attractive opportunity in energy and environmental research fields.

  11. Small-angle neutron scattering study of Fe-B and Fe-Ni-B metallic glasses

    International Nuclear Information System (INIS)

    Cser, L.; Kovacs, I.; Lovas, A.; Svab, E.; Zsigmond, G.

    1982-01-01

    Small-angle scattering of neutron (SANS) was analysed on Fe-B and Fe-Ni-B metallic glass ribbons by means of a double crystal small angle device and a neutron diffractometer. The dimensions of magnetic domains and small clusters were determined. An appreciable anisotropy of SANS intensity and surface scattering was observed. (orig.)

  12. Small-angle neutron scattering study of Fe-B and Fe-Ni-B metallic glasses

    International Nuclear Information System (INIS)

    Cser, L.; Kovacs, I.; Lovas, A.; Svab, E.; Zsigmond, Gy.

    1981-01-01

    Small-angle neutron scattering (SANS) on Fe-B and Fe-Ni-B metallic glass ribbons was analysed by means of a double-crystal small-angle device and a neutron diffractometer. The sizes of magnetic domains and small clusters were determined. An appreciable anisotropy of SANS intensity and surface scattering was observed. (author)

  13. Metal Injection Molding (MIM of NdFeB Magnets

    Directory of Open Access Journals (Sweden)

    Hartwig T.

    2014-07-01

    Full Text Available Due to the increased and unstable prices for Rare Earth elements there are activities to develop alternative hard magnetic materials. Reducing the amount of material necessary to produce complex sintered NdFeB magnets can also help to reduce some of the supply problem. Metal Injection Molding (MIM is able to produce near net shape parts and can reduce the amount of finishing to achieve final geometry. Although MIM of NdFeB has been patented and published fairly soon after the development of the NdFeB magnets there has never been an industrial production. This could be due to the fact that MIM was very young at that time and hardly developed. Thus, the feasibility of the process needs to be revaluated. This paper presents results of our work on determining the process parameters influencing the magnetic properties of the sintered magnets as well as the shrinkage during processing. The role of binder and powder loading on the alignment of the particles as well as on the carbon and oxygen contamination was examined.

  14. Fe-Cr-Ni system alloys

    International Nuclear Information System (INIS)

    Levin, F.L.

    1986-01-01

    Phase diagram of Fe-Cr-Ni system, which is the basic one for production of corrosion resistant alloys, is considered. Data on corrosion resistance of such alloys are correlated depending on a number of factors: quality and composition of modifying elements, corrosion medium, temperature, alloy structure, mechanical and thermal treatment. Grades of Fe-Ni-Cr alloys are presented, and fields of their application are pointed out

  15. Roles of Co element in Fe-based bulk metallic glasses utilizing industrial FeB alloy as raw material

    Directory of Open Access Journals (Sweden)

    Shouyuan Wang

    2017-08-01

    Full Text Available A series of Fe-based bulk metallic glasses were fabricated by a conventional copper mold casting method using a kind of Fe-B industrial raw alloy. It is found that Fe-B-Y-Nb bulk metallic glass with 3 at% of Co addition possesses the best glass forming ability, thermal stability, hardness, magnetic property and anti-corrosion property. The hardness test result indicates a synchronically trend with glass-forming ability parameters. The excellent glass-forming ability and a combination of good mechanical and functional properties suggest that the alloys in this work might be good candidates for commercial use.

  16. A Dilute-Limit Heat of Solution of 3d Transition Metals in Iron Studied with 57Fe Moessbauer Spectroscopy

    International Nuclear Information System (INIS)

    Chojcan, Jan

    2004-01-01

    The room-temperature 57 Fe Moessbauer spectra for binary iron-based solid solutions Fe 1-x D x with D=V, Cr, Mn and Co, were analysed in terms of binding energy E b between two D atoms in the Fe-D system. The extrapolated values of E b for x=0 were used for computation of the dilute-limit heat of solution of D metals in iron. The results were compared with those derived from calorimetric data concerning the heat of formation of the systems mentioned as well as with those resulting from the Miedema's model of alloys. The comparison shows that our Moessbauer spectroscopy findings are in a qualitative agreement with the available calorimetric data and they are at variance with corresponding Miedema's values for Fe-Mn and Fe-Co systems.

  17. Al-Ca and Al-Fe metal-metal composite strength, conductivity, and microstructure relationships

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Hyong June [Iowa State Univ., Ames, IA (United States)

    2011-01-01

    Deformation processed metal-metal composites (DMMC’s) are composites formed by mechanical working (i.e., rolling, swaging, or wire drawing) of two-phase, ductile metal mixtures. Since both the matrix and reinforcing phase are ductile metals, the composites can be heavily deformed to reduce the thickness and spacing of the two phases. Recent studies have shown that heavily drawn DMMCs can achieve anomalously high strength and outstanding combinations of strength and conductivity. In this study, Al-Fe wire composite with 0.07, 0.1, and 0.2 volume fractions of Fe filaments and Al-Ca wire composite with 0.03, 0.06, and 0.09 volume fractions of Ca filaments were produced in situ, and their mechanical properties were measured as a function of deformation true strain. The Al-Fe composites displayed limited deformation of the Fe phase even at high true strains, resulting in little strengthening effect in those composites. Al-9vol%Ca wire was deformed to a deformation true strain of 13.76. The resulting Ca second-phase filaments were deformed to thicknesses on the order of one micrometer. The ultimate tensile strength increased exponentially with increasing deformation true strain, reaching a value of 197 MPa at a true strain of 13.76. This value is 2.5 times higher than the value predicted by the rule of mixtures. A quantitative relationship between UTS and deformation true strain was determined. X-ray diffraction data on transformation of Al + Ca microstructures to Al + various Al-Ca intermetallic compounds were obtained at the Advanced Photon Source at Argonne National Laboratory. Electrical conductivity was measured over a range of true strains and post-deformation heat treatment schedules.

  18. Batch adsorption of heavy metals (Cu, Pb, Fe, Cr and Cd) from ...

    African Journals Online (AJOL)

    cinthia

    This study was carried out to evaluate the efficiency of metals (Cu, Fe, Pb, Cr and Cd) removal from mixed metal ions solution using coconut husk as adsorbent. The effects of varying contact time, initial metal ion concentration, adsorbent dose and pH on adsorption process of these metals were studied using synthetically ...

  19. Ferromagnetism in Fe-doped transition metal nitrides

    Science.gov (United States)

    Sharma, Ramesh; Sharma, Yamini

    2018-04-01

    Early transition metal mononitrides ScN and YN are refractory compounds with high hardness and melting points as well semiconducting properties. The presence of nitrogen vacancies in ScN/YN introduces asymmetric peaks in the density of states close to Fermi level, the same effects can be achieved by doping by Mn or Fe-atoms. Due to the substitution of TM atoms at Sc/Y sites, it was found that the p-d hybridization induces small magnetic moments at both Sc/Y and N sites giving rise to magnetic semiconductors (MS). From the calculated temperature dependent transport properties, the power factor and ZT is found to be lowered for doped ScN whereas it increases for doped YN. It is proposed that these materials have promising applications as spintronics and thermoelectric materials.

  20. Realization of a half-metallic state on bilayer WSe2 using doping transition metals (Cr, Mn, Fe, Co, Ni) in its interlayer

    Science.gov (United States)

    Yang, Guang; Yang, Yanmin; Ma, Hongran; Mao, Xiujuan; Li, Congcong; Li, Jie; Zhang, Qiang; Zhang, Zhidong; Yin, Fuxing; Li, Jia

    2018-03-01

    The structural, electronic and magnetic properties of Cr, Mn, Fe, Co and Ni-doped bilayer WSe2 are predicted by using first principles calculations. The doped transition-metal (TM) atoms show a covalent-binding with the nearest Se atoms. The calculated electronic structures reveal that the TM Cr, Mn, Fe and Co-doped bilayer WSe2 exhibits a half-metallic character with a 100% spin polarization at the Fermi level, and the reason is ascribed to the strong hybridization peak between the transition metals and the parent W and Se atoms. The Ni-doped bilayer WSe2 is still a semiconductor with nonmagnetism. The Fe-doped system has a robust stability of half-metallicity because there are three connected states peak spanning the Fermi level. The doping of Cr, Mn, Fe and Co atoms leads to a prominent total magnetism (0.93–3.65 {μ }{{B}} moment per unit cell), and an induced ∼0.3 {μ }{{B}} moment in parent W atoms is found in addition to the main contribution of TM atomic magnetism (0.71–3.33 {μ }{{B}} moment per atom). The predicted Cr, Mn, Fe and Co-doped bilayer WSe2 should be the candidate materials for spintronic devices due to their magnetic and half-metallic nature.

  1. Fabrication of γ-Fe2O3 Nanoparticles by Solid-State Thermolysis of a Metal-Organic Framework, MIL-100(Fe, for Heavy Metal Ions Removal

    Directory of Open Access Journals (Sweden)

    Shengtao Hei

    2014-01-01

    Full Text Available Porous γ-Fe2O3 nanoparticles were prepared via a solid-state conversion process of a mesoporous iron(III carboxylate crystal, MIL-100(Fe. First, the MIL-100(Fe crystal that served as the template of the metal oxide was synthesized by a low-temperature (<100°C synthesis route. Subsequently, the porous γ-Fe2O3 nanoparticles were fabricated by facile thermolysis of the MIL-100(Fe powders via a two-step calcination treatment. The obtained γ-Fe2O3 was characterized by X-ray diffraction (XRD, N2 adsorption, X-ray photoelectron spectroscopy (XPS, and scanning electron microscopy (SEM techniques, and then used as an adsorbent for heavy metal ions removal in water treatment. This study illustrates that the metal-organic frameworks may be suitable precursors for the fabrication of metal oxides nanomaterials with large specific surface area, and the prepared porous γ-Fe2O3 exhibits a superior adsorption performance for As(V and As(III ions removal in water treatment.

  2. Superconductivity and spin fluctuations in M-Zr metallic glasses (M = Cu, Ni, Co, and Fe)

    International Nuclear Information System (INIS)

    Altounian, Z.; Strom-Olsen, J.O.

    1983-01-01

    The superconducting transition temperature, upper critical field, and magnetic susceptibility have been measured in four binary metallic glass systems: Cu-Zr, Ni-Zr, Co-Zr, and Fe-Zr. For each alloy system, a full and continuous range of Zr-rich compositions accessible by melt spinning has been examined. For Cu-Zr, the range is 0.75>x>0.30; for Ni-Zr, 0.80>x>0.30; for Co-Zr, 0.80>x>0.48, and for Fe-Zr, 0.80>x>0.55 (x being the concentration of Zr in at. %). The results show clearly the influence of spin fluctuations in reducing the superconducting transition temperature. The data have been successfully analyzed using a modified form of the McMillan equation together with expressions for the Stoner enhanced magnetic susceptibility and the Ginsburg-Landau-Abrikosov-Gor'kov expression for the upper critical field

  3. On the atomic structure of Zr60Cu20Fe20 metallic glass

    Science.gov (United States)

    Kaban, I.; Jóvári, P.; Stoica, M.; Mattern, N.; Eckert, J.; Hoyer, W.; Beuneu, B.

    2010-10-01

    The structure of Zr60Cu20Fe20 metallic glass has been studied with high-energy x-ray diffraction, neutron diffraction and extended x-ray absorption spectroscopy and modelled with the reverse Monte Carlo simulation technique. It is found that Cu and Fe atoms prefer Zr as a nearest neighbour. The mean interatomic distance between Cu/Fe and Zr atoms in the glass is remarkably shorter than the sum of the respective atomic radii. The coordination numbers for Cu/Fe-Cu/Fe pairs are very close to each other, suggesting a regular distribution of Cu and Fe atoms in the Zr60Cu20Fe20 metallic glass.

  4. Search for half-metallic magnets with large half-metallic gaps in the quaternary Heusler alloys CoFeTiZ and CoFeVZ (Z=Al, Ga, Si, Ge, As, Sb)

    International Nuclear Information System (INIS)

    Xiong, Lun; Yi, Lin; Gao, G.Y.

    2014-01-01

    We investigate the electronic structure and magnetic properties of the twelve quaternary Heusler alloys CoFeTiZ and CoFeVZ (Z=Al, Ga, Si, Ge, As, Sb) by using the first-principles calculations. It is shown that only CoFeTiSi, CoFeTiAs and CoFeVSb are half-metallic ferromagnets with considerable half-metallic gaps of 0.31, 0.18 and 0.17 eV, respectively. CoFeTiAl and CoFeTiGa are conventional semiconductors, and other alloys exhibit nearly half-metallicity or their half-metallic gaps are almost zero eV. We also find that the half-metallicities of CoFeTiSi, CoFeTiAs and CoFeVSb can be preserved under appropriate uniform and in-plane strains. The considerable half-metallic gaps and the robust half-metallicities under uniform and in-plane strains make CoFeTiSi, CoFeTiAs and CoFeVSb promising candidates for spintronic applications. - Highlights: • CoFeTiSi, CoFeTiAs and CoFeVSb have considerable half-metallic gaps. • Total magnetic moments obey the Slater–Pauling behavior of quaternary Heusler half-metals. • CoFeTiSi, CoFeTiAs and CoFeVSb retain half-metallicity under uniform and in-plane strains

  5. Magnetism and metal insulator transition in FeSi and FeGe. Ab Initio investigations of the electronic structure; Magnetismus und Metall-Isolator-Uebergang in FeSi und FeGe. Ab-initio-Untersuchungen der elektronischen Struktur

    Energy Technology Data Exchange (ETDEWEB)

    Neef, Matthias

    2007-03-19

    Aim of this thesis was to reach by a systematic study of different ab initio procedures an improved description of the electronic properties of FeSi and FeGe. Central result is the itinerant description of FeSi as a semiconductor in the neighbourhood of a ferromagnetic instability. The regardment of the nonlocal exchange in the effective one-particle approximation leads to a metastable magnetic state scarcely above the magnetic ground state. The application of the hybrid functional leads to a 1st order metal-isolator transition for large lattice parameters: FeSi transforms at increasement of the lattice parameter from an unmagnetic isolator to a magnetic metal. A similar behavior is found in the isostructural compound FeGe. The two systems FeSi and FeGe were systematically and detailedly analyzed by means of ab initio procedures. Thereby the structural, electronic, and magnetic properties were studied with DFT and HF calculations. Both calculations with spin polarization and without spin polarization were performed.

  6. Spin-Orbit Effects in CoFeB/MgO Heterostructures with Heavy Metal Underlayers

    Science.gov (United States)

    Torrejon, Jacob; Kim, Junyeon; Sinha, Jaivardhan; Hayashi, Masamitsu

    2016-10-01

    We study effects originating from the strong spin-orbit coupling in CoFeB/MgO heterostructures with heavy metal (HM) underlayers. The perpendicular magnetic anisotropy at the CoFeB/MgO interface, the spin Hall angle of the heavy metal layer, current induced torques and the Dzyaloshinskii-Moriya interaction at the HM/CoFeB interfaces are studied for films in which the early 5d transition metals are used as the HM underlayer. We show how the choice of the HM layer influences these intricate spin-orbit effects that emerge within the bulk and at interfaces of the heterostructures.

  7. Effect of Iron Fe (II and Fe (III in a Binary System Evaluated Bioluminescent Method

    Directory of Open Access Journals (Sweden)

    Elena Sorokina

    2013-01-01

    Full Text Available The effect of iron ions Fe2+ and Fe3+ on the bioluminescent recombinant strain of Escherichia coli in a single-component and binary system. Found that for the bacteria E. coli Fe3+ ions are more toxic than Fe2+. Under the combined effect of iron toxicity increases, the percentage of luminescence quenching increases, but the value is much less than the sum of the indicator for the Fe2+ and Fe3+. The biological effect of insertion of iron is not proportional to their content in the mixture.

  8. Swapping metals in Fe- and Mn-dependent dioxygenases: Evidence for oxygen activation without a change in metal redox state

    Science.gov (United States)

    Emerson, Joseph P.; Kovaleva, Elena G.; Farquhar, Erik R.; Lipscomb, John D.; Que, Lawrence

    2008-01-01

    Biological O2 activation often occurs after binding to a reduced metal [e.g., M(II)] in an enzyme active site. Subsequent M(II)-to-O2 electron transfer results in a reactive M(III)-superoxo species. For the extradiol aromatic ring-cleaving dioxygenases, we have proposed a different model where an electron is transferred from substrate to O2 via the M(II) center to which they are both bound, thereby obviating the need for an integral change in metal redox state. This model is tested by using homoprotocatechuate 2,3-dioxygenases from Brevibacterium fuscum (Fe-HPCD) and Arthrobacter globiformis (Mn-MndD) that share high sequence identity and very similar structures. Despite these similarities, Fe-HPCD binds Fe(II) whereas Mn-MndD incorporates Mn(II). Methods are described to incorporate the nonphysiological metal into each enzyme (Mn-HPCD and Fe-MndD). The x-ray crystal structure of Mn-HPCD at 1.7 Å is found to be indistinguishable from that of Fe-HPCD, while EPR studies show that the Mn(II) sites of Mn-MndD and Mn-HPCD, and the Fe(II) sites of the NO complexes of Fe-HPCD and Fe-MndD, are very similar. The uniform metal site structures of these enzymes suggest that extradiol dioxygenases cannot differentially compensate for the 0.7-V gap in the redox potentials of free iron and manganese. Nonetheless, all four enzymes exhibit nearly the same KM and Vmax values. These enzymes constitute an unusual pair of metallo-oxygenases that remain fully active after a metal swap, implicating a different way by which metals are used to promote oxygen activation without an integral change in metal redox state. PMID:18492808

  9. Swapping metals in Fe- and Mn-dependent dioxygenases: Evidence for oxygen activation without a change in metal redox state

    Energy Technology Data Exchange (ETDEWEB)

    Emerson, Joseph P.; Kovaleva, Elena G.; Farquhar, Erik R.; Lipscomb, John D.; Oue, Jr., Lawrence (UMM)

    2008-07-21

    Biological O{sub 2} activation often occurs after binding to a reduced metal [e.g., M(II)] in an enzyme active site. Subsequent M(II)-to-O{sub 2} electron transfer results in a reactive M(III)-superoxo species. For the extradiol aromatic ring-cleaving dioxygenases, we have proposed a different model where an electron is transferred from substrate to O{sub 2} via the M(II) center to which they are both bound, thereby obviating the need for an integral change in metal redox state. This model is tested by using homoprotocatechuate 2,3-dioxygenases from Brevibacterium fuscum (Fe-HPCD) and Arthrobacter globiformis (Mn-MndD) that share high sequence identity and very similar structures. Despite these similarities, Fe-HPCD binds Fe(II) whereas Mn-MndD incorporates Mn(II). Methods are described to incorporate the nonphysiological metal into each enzyme (Mn-HPCD and Fe-MndD). The x-ray crystal structure of Mn-HPCD at 1.7 {angstrom} is found to be indistinguishable from that of Fe-HPCD, while EPR studies show that the Mn(II) sites of Mn-MndD and Mn-HPCD, and the Fe(II) sites of the NO complexes of Fe-HPCD and Fe-MndD, are very similar. The uniform metal site structures of these enzymes suggest that extradiol dioxygenases cannot differentially compensate for the 0.7-V gap in the redox potentials of free iron and manganese. Nonetheless, all four enzymes exhibit nearly the same K{sub M} and V{sub max} values. These enzymes constitute an unusual pair of metallo-oxygenases that remain fully active after a metal swap, implicating a different way by which metals are used to promote oxygen activation without an integral change in metal redox state.

  10. Na-Fe-Phosphate Globules in Impact Metal-Troilite Associations of Chelyabinsk Meteorite

    Science.gov (United States)

    Sharygin, V. V.; Karmanov, N. S.; Podgornykh, N. M.

    2016-08-01

    Multi- and monophase phosphate globules have been found in the impact metal-troilite aggregates of the Chelyabinsk chondrite. Their phase composition varies and they contain galileiite, sarcopside, graftonite and Na-Fe-phosphate Na2(Fe,Mn)5(PO4)4.

  11. Characterising the reactivity of metallic iron in Fe 0 /As-rock/H 2 O ...

    African Journals Online (AJOL)

    The intrinsic reactivity of 4 metallic iron materials (Fe0) was investigated in batch and column experiments. The Fe0 reactivity was characterised by the extent of aqueous fixation of in-situ leached arsenic (As). Air-homogenised batch experiments were conducted for 1 month with 10.0 g/. of an As-bearing rock (ore material) ...

  12. CO Hydrogenation over Transition Metals (Fe, Co, or Ni Modified K/Mo2C Catalysts

    Directory of Open Access Journals (Sweden)

    Minglin Xiang

    2013-01-01

    Full Text Available Transition metals (Fe, Co, or Ni modified K/Mo2C catalysts were prepared and investigated as catalysts for CO hydrogenation. The addition of Fe, Co, or Ni to K/Mo2C catalyst led to a sharp increase in both the activity and selectivity of C2+OH, but the promotion effects were quite different and followed the sequence: Ni > Co > Fe for the activity and Fe > Co > Ni for the alcohol selectivity. For the products distributions, it also displayed some differences; Co promoter showed much higher C5+ hydrocarbon selectivity than Fe or Ni promoter, but Fe or Co promoter gave lower methane selectivity than Ni promoter, and Fe promoter showed the highest C2=-C4= selectivity.

  13. Influence of Fe(2+)-catalysed iron oxide recrystallization on metal cycling.

    Science.gov (United States)

    Latta, Drew E; Gorski, Christopher A; Scherer, Michelle M

    2012-12-01

    Recent work has indicated that iron (oxyhydr-)oxides are capable of structurally incorporating and releasing metals and nutrients as a result of Fe2+-induced iron oxide recrystallization. In the present paper, we briefly review the current literature examining the mechanisms by which iron oxides recrystallize and summarize how recrystallization affects metal incorporation and release. We also provide new experimental evidence for the Fe2+-induced release of structural manganese from manganese-doped goethite. Currently, the exact mechanism(s) for Fe2+-induced recrystallization remain elusive, although they are likely to be both oxide-and metal-dependent. We conclude by discussing some future research directions for Fe2+-catalysed iron oxide recrystallization.

  14. Colloidal processing of Fe-based metal ceramic composites with high content of ceramic reinforcement

    Energy Technology Data Exchange (ETDEWEB)

    Escribano, J. A.; Ferrari, B.; Alvaredo, P.; Gordo, E.; Sanchez-Herencia, A. J.

    2013-07-01

    Major difficulties of processing metal-matrix composites by means of conventional powder metallurgy techniques are the lack of dispersion of the phases within the final microstructure. In this work, processing through colloidal techniques of the Fe-based metal-matrix composites, with a high content of a ceramic reinforcement (Ti(C,N) ), is presented for the first time in the literature. The colloidal approach allows a higher control of the powders packing and a better homogenization of phases since powders are mixed in a liquid medium. The chemical stability of Fe in aqueous medium determines the dispersion conditions of the mixture. The Fe slurries were formulated by optimising their zeta potential and their rheology, in order to shape bulk pieces by slip-casting. Preliminary results demonstrate the viability of this procedure, also opening new paths to the microstructural design of fully sintered Fe-based hard metal, with 50 vol. % of Ti(C,N) in its composition. (Author)

  15. Processing effects on the magnetostrictive and physical properties of SmFe2/metal composites

    Science.gov (United States)

    Pinkerton, F. E.; Capehart, T. W.; Herbst, J. F.; Brewer, E. G.; Murphy, C. B.

    1998-06-01

    Hot pressed SmFe2/Fe and SmFe2/Al composites combine the large magnetostriction of SmFe2 with the mechanical robustness of the Fe or Al matrix. Here we report the dependence of the magnetostriction, density, and mechanical hardness on processing parameters, specifically on the SmFe2 volume fill fraction and the consolidation temperature. The magnetostriction increases monotonically with increasing SmFe2 content, but both the density and hardness decrease; low fill fraction composites are within 10% of theoretical density and have hardnesses of 40-85 Rockwell B, whereas hot pressed SmFe2 powder alone has high porosity (exceeding 30%) and is too soft to register on the Rockwell B hardness scale. The best combination of properties lies in the range of 40%-60% SmFe2. Similar competition between magnetostriction and physical properties is observed as a function of the temperature used to consolidate the samples. The magnetostriction falls slowly as the hot press temperature increases, probably as a result of chemical reaction between the SmFe2 phase and the matrix metal. On the other hand, higher temperature improves the consolidation, resulting in higher density and hardness. These results demonstrate that the magnetostrictive and physical properties of SmFe2 composites can be tailored by adjusting the fill fraction and processing temperature.

  16. Pu(IV) and Fe(III) accumulation ability of heavy metal-tolerant soil fungi

    International Nuclear Information System (INIS)

    Levinskaite, L.; Smirnov, A.; Luksiene, B.; Druteikiene, R.; Remeikis, V.; Baltrunas, D.

    2009-01-01

    The work was aimed at studying abilities of soil microorganisms to participate in metal/radionuclide mobility processes by accumulating them. Soil microorganisms were treated with a mixture of heavy metals (Cr(III), Ni, Fe(III), Mn(II), Cd) in order to isolate the most tolerant ones. Among more metal-tolerant microorganisms microscopic fungi dominated. Tests of fungal tolerance towards each metal showed that the most tolerant fungi to almost all metals were Aspergillus niger, Penicillium oxalicum and Paecilomyces lilacinus. Accumulation ability of metal-tolerant fungi was tested using Pu(IV) and Fe(III). Investigation of Pu accumulation by fungal biomass showed that all the fungi accumulated Pu, and among the most effective radionuclide accumulators Eupenicillium sp., Penicillium oxalicum and Aspergillus niger could be mentioned. All the fungi showed high Fe-accumulation capacity. While growing in the medium with 1 mM iron, most fungi accumulated over 90% of Fe in their biomass. Very good accumulation and growth abilities in Fe-supplemented medium were demonstrated by Paecilomyces lilacinus. (authors)

  17. An Fe(TCNQ)2nanowire array on Fe foil: an efficient non-noble-metal catalyst for the oxygen evolution reaction in alkaline media.

    Science.gov (United States)

    Xie, Maowen; Xiong, Xiaoli; Yang, Lin; Shi, Xifeng; Asiri, Abdullah M; Sun, Xuping

    2018-02-27

    It is highly desirable to develop efficient and durable oxygen evolution reaction (OER) electrocatalysts. Herein, we report the in situ development of an Fe-(tetracyanoquinodimethane) 2 nanowire array on Fe foil (Fe(TCNQ) 2 /Fe) via a solution immersion method. As a non-noble-metal OER electrocatalyst, such Fe(TCNQ) 2 /Fe needs an overpotential of only 340 mV to drive a geometrical catalytic current density of 10 mA cm -2 in 1.0 M KOH. Notably, it also shows strong long-term electrochemical durability capable of maintaining its catalytic activity for at least 110 h.

  18. Fate of Fe, As in Acid Mine Drainage (AMD) was created Disused Metal Mine

    Science.gov (United States)

    Yu, H.; Kang, D. H.; Kim, S. J.; So, Y.

    2015-12-01

    This study is a natural reduction of Fe and As in AMD. AMD is produced by oxidation of pyrite, the iron, the sulfate mineral dissolution action. It is generated by the sulfide minerals, water, oxygen, the reaction of microorganisms in the underground. AMD is low pH due to dissolved minerals in the mine are different kinds of heavy metals will leach. If the flow out of mines and react with dissolved oxygen (DO) is increased, due to oxidation and microbiological activity of the Fe it is precipitated biomat is produced. This study area is Ilgwng disused mines in the Republic of Korea Busan Gijanggun. March to September 2010 taken by the AMD and biomat analyze Fe and As. The main mineral is Chalcopyrite (Cu2Fe2S4), Arsenopyrite (FeAsS), Pyrite (FeS2), Pyrrhotite (Fe1-xS), Sphalerite (ZnS), Galena (PbS), Scheelite (CaWO4), Wolframite ((Fe, Mn)WO4) and the like. Analysis of the AMD of underground pH 2.4~2.8, DO 1.3~4.8mg/L, Fe 474.3~178.8mg/L, As 0~3.2mg/L. Analysis AMD of the flow out of mine pH 2.3~2.9, DO 6.7~9.5mg/L, Fe 81.9~438.7L, As 0~2.8mg/L. The content of Fe in the biomat is 244.242mg/kg, the content of As is 5647mg/kg in the adsorption reaction of the Fe. AMD of disused metal mine mineral leaching occur in a reducing environment, in an oxidizing environment it caused precipitation and adsorption reactions.

  19. Preparation, thermal stability, and magnetic properties of Fe-Zr-Mo-W-B bulk metallic glass

    International Nuclear Information System (INIS)

    Liu, D.Y.; Sun, W.S.; Wang, A.M.; Zhang, H.F.; Hu, Z.Q.

    2004-01-01

    A bulk metallic glass (BMG) cylinder of Fe 60 Co 8 Zr 10 Mo 5 W 2 B 15 with a diameter of 1.5 mm was prepared by copper mould casting of industrial raw materials. The amorphous state and the crystallization behavior were investigated by X-ray diffraction (XRD). The thermal stability parameters, such as glass transition temperature (T g ), crystallization temperature (T x ), supercooled liquid region (ΔT x ) between T g and T x , and reduced glass transition temperature T rg (T g /T m ) were measured by differential scanning calorimetry (DSC) to be 891, 950, 59 K, and 0.62, respectively. The crystallization process took place through a single stage, and involved crystallization of the phases α-Fe, ZrFe 2 , Fe 3 B, MoB 2 , Mo 2 FeB 2 , and an unknown phase, as determined by X-ray analysis of the sample annealed for 1.5 ks at 1023 K, 50 K above the DSC peak temperature of crystallization. Moessbauer spectroscopy was studied for this alloy. The spectra exhibit a broadened and asymmetric doublet-like structure that indicated paramagnetic behavior and a fully amorphous structure. α-Fe was found in the amorphous matrix for a cylinder with a diameter of 2.5 mm. The success of synthesis of the Fe-based bulk metallic glass from industrial materials is important for the future progress in research and practical application of new bulk metallic glasses

  20. Chloride corrosion in biomass-fired boilers – Fe-O-Cl system thermodynamic analysis

    Directory of Open Access Journals (Sweden)

    Kaczmarczyk Robert

    2016-01-01

    The paper presents a thermodynamic analysis of chloride-induced corrosion in the Fe-O-Cl system. The ranges of the metallic, oxide and chloride phase stability are determined within the temperature range T = 750-1000 K. Based on the parametric equations the equilibrium concentration of gaseous phase determined by Deacon reaction are presented. The effect of H2O concentration in the gaseous phase on high-temperature corrosion process and gaseous NaCl influence on NaFeO2 formation in the passive oxide scale layer (FeO/Fe3O4/Fe2O3 are discussed as well. The results are correlated with available in the literature laboratory experimental data and industrial corrosion process observations. Presented thermodynamic analysis is compared with assumptions of “active oxidation” model. The results may be used for experimental research prediction and a corrosion prevention in the industry.

  1. Distribution of heavy metals (Cu and Fe) in sea water of Gresik coastal area

    Science.gov (United States)

    Nindyapuspa, Ayu; Ni'am, Achmad Chusnun

    2018-02-01

    The improvement of industrial activities at Gresik Regency will increase the heavy metals concentration on the seawater at Gresik Regency. Therefore, the research of Fe and Cr distribution on the seawater at Gresik Regency has been conducted. Methods that were used is sampling by Nansen water sampler at three sampling points (housing in northern coastal Gresik Regency, Maspion V Industrial Estate, and Petrokimia Port). Samples were analyzed by Atomic Absorption Spectrophotometry (AAS) to determine the concentration of heavy metals. The results showed that the highest Fe and Cr concentration are located at Maspion V Industrial Estate (0.452 mg/L and 0.081 mg/L respectively). Meanwhile, Fe and Cr concentrations at the housing in northern coastal are (0.408 mg/L and 0.081 mg/L respectively). The concentration of Fe and Cr at Petrokimia Port are 0.174 mg/L and 0.021 mg/L respectively.

  2. Manganese Abundances in the Stars with Metallicities -1 <[Fe/H]< +0.3

    Science.gov (United States)

    Mishenina, T.; Gorbaneva, T.; Pignatari, M.; Thielemann, F.-K.; Korotin, S.

    2018-01-01

    We estimate the Mn abundances in the atmospheres of 247 F-G-K-type dwarf stars belonging to the thin and thick disk populations in the metallicity range -1 LTE approximation; the synthetic spectrum for the Mn lines was computed accounting for the hyperfine structure. Starting from the results obtained, we discuss the evolution of the [Mn/Fe] ratio with respect to [Fe/H] in the galactic disk.

  3. Transition metals and PET - the challenge 52Fe

    International Nuclear Information System (INIS)

    Calonder, C.; Leenders, K.L.

    1997-01-01

    Methodology and limits of studying the biodistribution of 52 Fe in the brain with positron emission tomography (PET). The influence of the iron's daughter nuclide 52m Mn quantification of physiological relevant parameters is of special interest. (author) 1 fig., 3 refs

  4. Evolutionary analysis of iron (Fe) acquisition system in Marchantia polymorpha.

    Science.gov (United States)

    Lo, Jing-Chi; Tsednee, Munkhtsetseg; Lo, Ying-Chu; Yang, Shun-Chung; Hu, Jer-Ming; Ishizaki, Kimitsune; Kohchi, Takayuki; Lee, Der-Chuen; Yeh, Kuo-Chen

    2016-07-01

    To acquire appropriate iron (Fe), vascular plants have developed two unique strategies, the reduction-based strategy I of nongraminaceous plants for Fe(2+) and the chelation-based strategy II of graminaceous plants for Fe(3+) . However, the mechanism of Fe uptake in bryophytes, the earliest diverging branch of land plants and dominant in gametophyte generation is less clear. Fe isotope fractionation analysis demonstrated that the liverwort Marchantia polymorpha uses reduction-based Fe acquisition. Enhanced activities of ferric chelate reductase and proton ATPase were detected under Fe-deficient conditions. However, M. polymorpha did not show mugineic acid family phytosiderophores, the key components of strategy II, or the precursor nicotianamine. Five ZIP (ZRT/IRT-like protein) homologs were identified and speculated to be involved in Fe uptake in M. polymorpha. MpZIP3 knockdown conferred reduced growth under Fe-deficient conditions, and MpZIP3 overexpression increased Fe content under excess Fe. Thus, a nonvascular liverwort, M. polymorpha, uses strategy I for Fe acquisition. This system may have been acquired in the common ancestor of land plants and coopted from the gametophyte to sporophyte generation in the evolution of land plants. © 2016 The Authors. New Phytologist © 2016 New Phytologist Trust.

  5. SEPARATION OF Ca AND Fe METAL ION IN SOURCE WATER BY ADSORPTION COLUMN TECHNIC WITH LOCAL ZEOLITE AND ACTIVE CARBON

    Directory of Open Access Journals (Sweden)

    Suyanta Suyanta

    2016-04-01

    Full Text Available This research aims are to separate of Ca and Fe metal ion in source water, with local zeolite and active carbon by adsorption column technic. Efficiency of separation are control by adsorption time and size of zeolite. Method that used was column adsorption with a flow system in which sample is applied to the filtration tube containing zeolite and active carbon. Initial and final concentrations of the samples were analyzed using Atomic Adsorption Spectrophotometer instrument. The results obtained shows that ability adsorption of zeolite to Ca and Fe metal ion are a good. Zeolite 1 (10 mesh can reduce iron concentration until 93.98 % and zeolite 2 (5mesh until 98.88% for 1 – 4 week range time. Whereas reducing of calcium concentration is not good, until 2 week period time adsorption of calcium ion is about 50%.   Keywords: adsorption, zeolite, source water

  6. Impact of water saturation level on arsenic and metal mobility in the Fe-amended soil.

    Science.gov (United States)

    Kumpiene, Jurate; Ragnvaldsson, Daniel; Lövgren, Lars; Tesfalidet, Solomon; Gustavsson, Björn; Lättström, Anders; Leffler, Per; Maurice, Christian

    2009-01-01

    The impact of water saturation level (oxidizing-reducing environment) on As and metal solubility in chromium, copper, arsenic (CCA)-contaminated soil amended with Fe-containing materials was studied. The soil was mixed with 0.1 and 1 wt% of iron grit (Fe(0)) and 1, 7 and 15 wt% of oxygen scarfing granulate (OSG, a by-product of steel processing). Solubility of As and metals was evaluated by a batch leaching test and analysis of soil pore water. Soil saturation with water greatly increased As solubility in the untreated as well as in the Fe-amended soil. This was related to the reductive dissolution of Fe oxides and increased concentration of As(III) species. Fe amendments showed As reducing capacity under both oxic and anoxic conditions. The cytotoxicity of the soil pore water correlated with the concentration of As(III). The Fe-treatments as well as water saturation of soil were less significant for the solubility of Cu, Cr and Zn than for As. The batch leaching test used for waste characterization substantially underestimated As solubility that could occur under water-saturated (anaerobic) conditions. In the case of soil landfilling, other techniques than Fe-stabilization of As containing soil should be considered.

  7. Adhesive and Cohesive Strength in FeB/Fe2B Systems

    Science.gov (United States)

    Meneses-Amador, A.; Blancas-Pérez, D.; Corpus-Mejía, R.; Rodríguez-Castro, G. A.; Martínez-Trinidad, J.; Jiménez-Tinoco, L. F.

    2018-01-01

    In this work, FeB/Fe2B systems were evaluated by the scratch test. The powder-pack boriding process was performed on the surface of AISI M2 steel. The mechanical parameters, such as yield stress and Young's modulus of the boride layer, were obtained by the instrumented indentation technique. Residual stresses produced on the boride layer were estimated by using the x-ray diffraction (XRD) technique. The scratch test was performed in order to evaluate the cohesive/adhesive strength of the FeB/Fe2B coating. In addition, a numerical evaluation of the scratch test on boride layers was performed by the finite element method. Maximum principal stresses were related to the failure mechanisms observed by the experimental scratch test. Shear stresses at the interfaces of the FeB/Fe2B/substrate system were also evaluated. Finally, the results obtained provide essential information about the effect of the layer thickness, the residual stresses, and the resilience modulus on the cohesive/adhesive strength in FeB/Fe2B systems.

  8. Route and Regulation of Zinc, Cadmium, and Iron Transport in Rice Plants (Oryza sativa L. during Vegetative Growth and Grain Filling: Metal Transporters, Metal Speciation, Grain Cd Reduction and Zn and Fe Biofortification

    Directory of Open Access Journals (Sweden)

    Tadakatsu Yoneyama

    2015-08-01

    Full Text Available Zinc (Zn and iron (Fe are essential but are sometimes deficient in humans, while cadmium (Cd is toxic if it accumulates in the liver and kidneys at high levels. All three are contained in the grains of rice, a staple cereal. Zn and Fe concentrations in rice grains harvested under different levels of soil/hydroponic metals are known to change only within a small range, while Cd concentrations show greater changes. To clarify the mechanisms underlying such different metal contents, we synthesized information on the routes of metal transport and accumulation in rice plants by examining metal speciation, metal transporters, and the xylem-to-phloem transport system. At grain-filling, Zn and Cd ascending in xylem sap are transferred to the phloem by the xylem-to-phloem transport system operating at stem nodes. Grain Fe is largely derived from the leaves by remobilization. Zn and Fe concentrations in phloem-sap and grains are regulated within a small range, while Cd concentrations vary depending on xylem supply. Transgenic techniques to increase concentrations of the metal chelators (nicotianamine, 2′-deoxymugineic acid are useful in increasing grain Zn and Fe concentrations. The elimination of OsNRAMP5 Cd-uptake transporter and the enhancement of root cell vacuolar Cd sequestration reduce uptake and root-to-shoot transport, respectively, resulting in a reduction of grain Cd accumulation.

  9. Structure Analyses of Fe-based Metallic Glasses by Electron Diffraction

    Directory of Open Access Journals (Sweden)

    Akihiko Hirata

    2010-12-01

    Full Text Available Nanoscale structural information of amorphous structures has become obtainable by using nanobeam electron diffraction in combination with high resolution imaging. In addition, accurate radial distribution function analysis using energy filter has also become available to know averaged amorphous structures. In this paper, we introduce some applications of these techniques, especially to several Fe-based metallic glasses. On the basis of these results, we discuss a relationship between the glass structure and the glass stability in Fe-based metallic glasses

  10. Non-repeatability of large plasticity for Fe-based bulk metallic glasses

    International Nuclear Information System (INIS)

    Yang, Weiming; Sun, Baoan; Zhao, Yucheng; Li, Qiang; Hou, Long; Luo, Ning; Dun, Chaochao; Zhao, Chengliang; Ma, Zhanguo; Liu, Haishun; Shen, Baolong

    2016-01-01

    Serrated flow is an essential characteristic of the plastic deformation of metallic glasses. Under restricted loading conditions, the formation and expansion of shear bands act as the serrated flow of stress-strain curves in metallic glasses. In this work, serrated flows in Fe 50 Ni 30 P 13 C 7 glassy samples with different plasticity were studied. The distribution histogram shows a monotonically decreasing trend during the initial deformation stage (i.e., the plastic deformation in the range of 0–8%), whereas in the following deformation stage (i.e., a plastic deformation of 8–14%), the stress drop frequency distribution presents both a monotonically decreasing distribution and a peak shape similar to chaotic dynamics. It is shown that the spatial evolution behavior of shear bands in Fe 50 Ni 30 P 13 C 7 metallic glasses evolved from self-organized critical to chaotic dynamics in the form of serrated flow, which reveals the origin of discrete plasticity of Fe-based bulk metallic glasses. This study has potential applications for understanding the plastic deformation mechanism. - Highlights: • Two-stage deformation mechanism in Fe-based bulk metallic glasses. • Distribution of the stress drop amplitude is significantly different at two stages. • The stages are related to multiple shear bands and discrete plasticity.

  11. Non-repeatability of large plasticity for Fe-based bulk metallic glasses

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Weiming [State Key Laboratory for Geomechanics and Deep Underground Engineering, School of Mechanics and Civil Engineering, School of Sciences, China University of Mining and Technology, Xuzhou 221116 (China); Sun, Baoan [Department of Mechanical and Biomedical Engineering, City University of Hong Kong (Hong Kong); Zhao, Yucheng, E-mail: zhaoyc1972@163.com [State Key Laboratory for Geomechanics and Deep Underground Engineering, School of Mechanics and Civil Engineering, School of Sciences, China University of Mining and Technology, Xuzhou 221116 (China); Li, Qiang [School of Physics Science and Technology, Xinjiang University, Urumqi, Xinjiang 830046 (China); Hou, Long; Luo, Ning [State Key Laboratory for Geomechanics and Deep Underground Engineering, School of Mechanics and Civil Engineering, School of Sciences, China University of Mining and Technology, Xuzhou 221116 (China); Dun, Chaochao [Department of Physics, Wake Forest University, Winston Salem, NC 27109 (United States); Zhao, Chengliang [Key Laboratory of Magnetic Materials and Devices, Ningbo Institute of Materials Technology & Engineering, Chinese Academy of Sciences, Ningbo 315201 (China); Ma, Zhanguo [State Key Laboratory for Geomechanics and Deep Underground Engineering, School of Mechanics and Civil Engineering, School of Sciences, China University of Mining and Technology, Xuzhou 221116 (China); Liu, Haishun, E-mail: liuhaishun@126.com [State Key Laboratory for Geomechanics and Deep Underground Engineering, School of Mechanics and Civil Engineering, School of Sciences, China University of Mining and Technology, Xuzhou 221116 (China); Shen, Baolong [School of Materials Science and Engineering, Southeast University, Nanjing 211189 (China)

    2016-08-15

    Serrated flow is an essential characteristic of the plastic deformation of metallic glasses. Under restricted loading conditions, the formation and expansion of shear bands act as the serrated flow of stress-strain curves in metallic glasses. In this work, serrated flows in Fe{sub 50}Ni{sub 30}P{sub 13}C{sub 7} glassy samples with different plasticity were studied. The distribution histogram shows a monotonically decreasing trend during the initial deformation stage (i.e., the plastic deformation in the range of 0–8%), whereas in the following deformation stage (i.e., a plastic deformation of 8–14%), the stress drop frequency distribution presents both a monotonically decreasing distribution and a peak shape similar to chaotic dynamics. It is shown that the spatial evolution behavior of shear bands in Fe{sub 50}Ni{sub 30}P{sub 13}C{sub 7} metallic glasses evolved from self-organized critical to chaotic dynamics in the form of serrated flow, which reveals the origin of discrete plasticity of Fe-based bulk metallic glasses. This study has potential applications for understanding the plastic deformation mechanism. - Highlights: • Two-stage deformation mechanism in Fe-based bulk metallic glasses. • Distribution of the stress drop amplitude is significantly different at two stages. • The stages are related to multiple shear bands and discrete plasticity.

  12. Synthesis of Mg2FeH6 containing as additives transition metal and transition metal fluorides or carbon

    International Nuclear Information System (INIS)

    Zepon, G.; Leiva, D.R.; Botta, W.J.

    2010-01-01

    The Mg 2 FeH 6 is a promising way of storing hydrogen in solid form, composed by elements that have low cost and, at the same time, high volumetric storage density: 150 kg H 2 /m 3 . However, this complex hydride is not easily synthesized as a single phase material. The hydrogen sorption high temperature and slow kinetics are the major limitations for the practical application of the Mg 2 FeH 6 as a hydrogen storage material. Little is known about the effects of additives in Mg 2 FeH 6 based nanocomposites in this work were synthesized by MAE under hydrogen atmosphere nanocomposites based on Mg 2 FeH 6 containing additives as transition metals, transition metals fluorides of transition metals or carbon, in order to obtain information on the effects of the selected additives. To this end, we used characterization techniques such as XRD, SEM and TEM, thermal analysis by DSC and curves made in apparatus PCT.(author)

  13. Development of Fe-based bulk metallic glasses as potential biomaterials.

    Science.gov (United States)

    Li, Shidan; Wei, Qin; Li, Qiang; Jiang, Bingliang; Chen, You; Sun, Yanfei

    2015-01-01

    A new series of Fe80-x-yCrxMoyP13C7 (x = 10, y = 10; x = 20, y = 5; x = 2 0, y = 10, all in at.%) bulk metallic glasses (BMGs) with the maximum diameter of 6mm have been developed for biomedical implant application by the combination method of fluxing treatment and J-quenching technique. The corrosion performance of the present Fe-based BMGs is investigated in both Hank's solution (pH = 7.4) and artificial saliva solution (pH = 6.3) at 37 °C by electrochemical measurements. The result indicates that the corrosion resistance of the present Fe-based BMGs in the above two simulated body solutions is much better than that of biomedical 316 L stainless steel (316 L SS), and approaching that of Ti6Al4V biomedical alloy (TC4). The concentrations of Fe, Ni and Cr ions released into the Hank's solution and artificial saliva solution from the present Fe-based BMGs after potentiodynamic polarization are significant lower than that released from 316 L SS. The biocompatibility of the present Fe-based BMGs is evaluated through the in vitro test of NIH3T3 cells culture in the present Fe-based BMG extraction media for 1, 3 and 5 days. The result indicates that the present Fe-based BMGs exhibit no cytotoxicity to NIH3T3 cells. And the test result of the cell adhesion and growth on the surface of the samples indicates that the present Fe-based BMGs exhibit the better cell viability compared with 316 L SS and TC4 biomedical alloys. The present Fe-based BMGs, especially Fe55Cr20Mo5P13C7 BMG, exhibit good glass formation ability, the high corrosion resistance and excellent biocompatibility, suggesting their promising potential as biomaterials. Copyright © 2015 Elsevier B.V. All rights reserved.

  14. FeSiBP bulk metallic glasses with high magnetization and excellent magnetic softness

    Energy Technology Data Exchange (ETDEWEB)

    Makino, Akihiro [Institute for Materials Research, Tohoku University, 2-1-1 Katahira, Sendai 980-8577 (Japan)], E-mail: amakino@imr.tohoku.ac.jp; Kubota, Takeshi; Chang, Chuntao [Institute for Materials Research, Tohoku University, 2-1-1 Katahira, Sendai 980-8577 (Japan); Makabe, Masahiro [Makabe R and D Co., Ltd., 3-1-25 Nagatake, Sendai 983-0036 (Japan); Inoue, Akihisa [Tohoku University, 2-1-1 Katahira, Sendai 980-8577 (Japan)

    2008-10-15

    Fe-based amorphous alloy ribbons are one of the major soft magnetic materials, because of their superior magnetic properties such as the relatively high saturation magnetization (J{sub s}) of 1.5-1.6 T and good magnetic softness. However, the preparation of the ordinary amorphous magnetic alloys requires cooling rates higher than 10{sup 4} K/s due to the low glass-forming ability (GFA) and thus restricts the material outer shape. Recently, Fe-metalloid-based bulk metallic glasses (BMGs) containing glass-forming elements such as Al, Ga, Nb, Mo, Y and so forth have been developed. These alloys have high GFA, leading to the formation of BMG rod with diameters of mm-order. However, the glass-forming metal elements in BMGs result in a remarkable decrease in magnetization. Basically, J{sub s} depends on Fe content; hence, high J{sub s} requires high Fe content in the Fe-based amorphous alloys or BMGs. On the other hand, high GFA requires a large amount of glass-forming elements in the alloys, which results in lower Fe content. Therefore, in substances, the coexistence of high J{sub s} and high GFA is difficult. Since this matter should be immensely important from academia to industry in the material field, a great deal of effort has been devoted; however, it has remained unsolved for many years. In this paper, we present a novel Fe-rich FeSiBP BMG with high J{sub s} of 1.51 T comparable to the ordinary Fe-Si-B amorphous alloy now in practical use as well as with high GFA leading to a rod-shaped specimen of 2.5 mm in diameter, obtained by Cu-mold casting in air.

  15. Bimetallic Porous Iron (pFe) Materials for Remediation/Removal of Tc from Aqueous Systems

    Energy Technology Data Exchange (ETDEWEB)

    Li, D. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2017-09-29

    Remediation of Tc remains an unresolved challenge at SRS and other DOE sites. The objective of this project was to develop novel bimetallic porous iron (pFe) materials for Tc removal from aqueous systems. We showed that the pFe is much more effective in removing TcO4 - (×30) and ReO4 - (×8) from artificial groundwater than granular iron. Tc K-edge XANES spectroscopy indicated that Tc speciation on the pFe was 18% adsorbed TcO4 -, 28% Tc(IV) in Tc dioxide and 54% Tc(IV) into the structure of Fe hydroxide. A variety of catalytic metal nanoparticles (i.e., Ni, Cu, Zn, Ag, Sn and Pd) were successfully deposited on the pFe using scalable chemical reduction methods. The Zn-pFe was outstanding among the six bimetallic pFe materials, with a capacity increase of >100% for TcO4 - removal and of 50% for ReO4 - removal, compared to the pFe. These results provide a highly applicable platform for solving critical DOE and industrial needs related to nuclear environmental stewardship and nuclear power production.

  16. Thermodynamics of Fe(II)Fe(III) oxide systems I. Hydrothermal Fe3O4

    Science.gov (United States)

    Bartel, J.J.; Westrum, E.F.; Haas, J.L.

    1976-01-01

    The heat capacity of a hydrothermally-prepared polycrystalline sample of Fe3O4 was measured from 53 to 350 K, primarily to study the thermophysics of the Verwey transitions. Although the bifurcation of the transition was confirmed, the sample was found to contain traces of manganese. The observed transition temperatures of 117.0 and 123.0 K are 3.7 and 4.2 K higher respectively than those found in pure Fe3O4. Ancillary analytical results are consistent and indicate a stoichiometry of Mn0.008Fe2.992O4 for this material. Characteristics in the transition region are ascribed to dopant effects. ?? 1976.

  17. Comparison of metals extractability from Al/Fe-based drinking water treatment residuals.

    Science.gov (United States)

    Wang, Changhui; Bai, Leilei; Pei, Yuansheng; Wendling, Laura A

    2014-12-01

    Recycling of drinking water treatment residuals (WTRs) as environment amendments has attracted substantial interest due to their productive reuse concomitant with waste minimization. In the present study, the extractability of metals within six Al/Fe-hydroxide-comprised WTRs collected throughout China was investigated using fractionation, in vitro digestion and the toxicity characteristic leaching procedure (TCLP). The results suggested that the major components and structure of the WTRs investigated were similar. The WTRs were enriched in Al, Fe, Ca, and Mg, also contained varying quantities of As, Ba, Be, Cd, Co, Cr, Cu, K, Mn, Mo, Na, Ni, Pb, Sr, V, and Zn, but Ag, Hg, Sb, and Se were not detected. Most of the metals within the WTRs were largely non-extractable using the European Community Bureau of Reference (BCR) procedure, but many metals exhibited high bioaccessibility based on in vitro digestion. However, the WTRs could be classified as non-hazardous according to the TCLP assessment method used by the US Environmental Protection Agency (USEPA). Further analysis showed the communication factor, which is calculated as the ratio of total extractable metal by BCR procedure to the total metal, for most metals in the six WTRs, was similar, whereas the factor for Ba, Mn, Sr, and Zn varied substantially. Moreover, metals in the WTRs investigated had different risk assessment code. In summary, recycling of WTRs is subject to regulation based on assessment of risk due to metals prior to practical application.

  18. Comprehensive and Reproducible Phosphopeptide Enrichment Using Iron Immobilized Metal Ion Affinity Chromatography (Fe-IMAC) Columns

    NARCIS (Netherlands)

    Ruprecht, Benjamin; Koch, Heiner; Medard, Guillaume; Mundt, Max; Kuster, Bernhard; Lemeer, Simone

    Advances in phosphopeptide enrichment methods enable the identification of thousands of phosphopeptides from complex samples. Current offline enrichment approaches using TiO2, Ti, and Fe immobilized metal ion affinity chromatography (IMAC) material in batch or microtip format are widely used, but

  19. Ab initio study of solute transition-metal interactions with point defects in bcc Fe

    NARCIS (Netherlands)

    Olsson, P.; Klaver, T.P.C.; Domain, C.

    2010-01-01

    The properties of 3d, 4d, and 5d transition-metal elements in ?-Fe have been studied using ab initio density-functional theory. The intrinsic properties of the solutes have been characterized as well as their interaction with point defects. Vacancies and interstitials of (110) and (111) orientations

  20. Formation of a metallic glass by thermal decomposition of Fe(CO)5

    DEFF Research Database (Denmark)

    Wonterghem, Jacques van; Mørup, Steen; Charles, Stuart W.

    1985-01-01

    Iron pentacarbonyl has been thermally decomposed in an organic liquid. Mössbauer spectroscopy and x-ray diffraction studies show that the sample contains small particles of a metallic glass. Annealing of the particles at 523 K results in crystallization of the particles into a mixture of α-Fe and χ...

  1. Bioaccumulation of heavy metals (Cu, Zn, Fe) in freshwater snail ...

    African Journals Online (AJOL)

    Viscera), 83.99 – 373.93 (Shell), which suggest that ingestion may be the main uptake route of these essential metals. A holistic biomonitoring approach is therefore proposed for these impacted areas to guide regulators in a direction of improvement.

  2. Ni3FeN-Supported Fe3Pt Intermetallic Nanoalloy as a High-Performance Bifunctional Catalyst for Metal-Air Batteries.

    Science.gov (United States)

    Cui, Zhiming; Fu, Gengtao; Li, Yutao; Goodenough, John B

    2017-08-07

    Electrocatalysts for both the oxygen reduction and evolution reactions (ORR and OER) are vital for the performances of rechargeable metal-air batteries. Herein, we report an advanced bifunctional oxygen electrocatalyst consisting of porous metallic nickel-iron nitride (Ni 3 FeN) supporting ordered Fe 3 Pt intermetallic nanoalloy. In this hybrid catalyst, the bimetallic nitride Ni 3 FeN mainly contributes to the high activity for the OER while the ordered Fe 3 Pt nanoalloy contributes to the excellent activity for the ORR. Robust Ni 3 FeN-supported Fe 3 Pt catalysts show superior catalytic performance to the state-of-the-art ORR catalyst (Pt/C) and OER catalyst (Ir/C). The Fe 3 Pt/Ni 3 FeN bifunctional catalyst enables Zn-air batteries to achieve a long-term cycling performance of over 480 h at 10 mA cm -2 with high efficiency. The extraordinarily high performance of the Fe 3 Pt/Ni 3 FeN bifunctional catalyst makes it a very promising air cathode in alkaline electrolyte. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  3. Synthesis of Fe-Al nanoparticles by hydrogen plasma-metal reaction

    CERN Document Server

    Liu Tong; Li Xing Guo

    2003-01-01

    Fe-Al nanoparticles of eight kinds have been prepared by hydrogen plasma-metal reaction. The morphology, crystal structure, and chemical composition of the nanoparticles obtained were investigated by transmission electron microscopy (TEM), x-ray diffractometry (XRD), and induction-coupled plasma spectroscopy. The particle size was determined by TEM and Brunaumer-Emmet-Teller gas adsorption. It was found that all the nanoparticles have spherical shapes, with average particle size in the range of 29-46 nm. The oxide layer in nanoparticles containing Al after passivation is not observable by XRD and TEM. The Al contents in Fe-Al ultrafine particles are about 1.2-1.5 times those in the master alloys. The evaporation speeds of Al and Fe in Fe-Al alloys are mutually accelerated at a certain composition. The crystal structures of the Fe-Al nanoparticles vary with the composition of the master alloys. Pure Fe sub 3 Al (D0 sub 3) and FeAl (B2) structures are successfully produced with 15 and 25 at.% Al in bulks, respe...

  4. The vertical metallicity gradient of the Milky Way disk: transitions in [α/Fe] populations

    International Nuclear Information System (INIS)

    Schlesinger, Katharine J.; Johnson, Jennifer A.; Rockosi, Constance M.; Lee, Young Sun; Beers, Timothy C.; Harding, Paul; Allende Prieto, Carlos; Bird, Jonathan C.; Schönrich, Ralph; Yanny, Brian; Schneider, Donald P.; Weaver, Benjamin A.; Brinkmann, Jon

    2014-01-01

    Using G dwarfs from the Sloan Extension for Galactic Understanding and Exploration (SEGUE) survey, we have determined the vertical metallicity gradient in the Milky Way's disk and examined how this gradient varies for different [α/Fe] subsamples. Our sample contains over 40,000 stars with low-resolution spectroscopy over 144 lines of sight. It also covers a significant disk volume, between ∼0.3 and 1.6 kpc from the Galactic plane, and allows us to examine the disk in situ, whereas previous analyses were more limited in scope. Furthermore, this work does not presuppose a disk structure, whether composed of a single complex population or distinct thin and thick disk components. We employ the SEGUE Stellar Parameter Pipeline to obtain estimates of stellar parameters, [Fe/H], and [α/Fe] and extract multiple volume-complete subsamples of approximately 1000 stars each. Based on SEGUE's target-selection algorithm, we adjust each subsample to determine an unbiased picture of disk chemistry; consequently, each individual star represents the properties of many. The metallicity gradient is –0.243 −0.053 +0.039 dex kpc –1 for the entire sample, which we compare to various literature results. This gradient stems from the different [α/Fe] populations inhabiting different ranges of height above the Galactic plane. Each [α/Fe] subsample shows little change in median [Fe/H] with height. If we associate [α/Fe] with age, the negligible gradients of our [α/Fe] subsamples suggest that stars formed in different epochs exhibit comparable vertical structure, implying similar star formation processes and evolution.

  5. Characterization and properties of sintered WC–Co and WC–Ni–Fe hard metal alloys

    International Nuclear Information System (INIS)

    Chang, Shih-Hsien; Chen, Song-Ling

    2014-01-01

    Highlights: • WC–Ni–Fe alloy sintered at 1400 °C had the highest hardness (HRA 85.3 ± 0.5). • The optimal WC–Ni–Fe sintered alloy possessed the highest TRS value (2524.5 ± 1.0 MPa). • The fracture toughness of the sintered WC–Ni–Fe alloys is mainly provided by the Ni–Fe binders. • WC–Ni–Fe sintered alloy possessed the highest fracture toughness of K IC (15.1 MPa m 1/2 ). • The WC–Ni–Fe sintered alloy had the much better corrosion resistance in 0.15 M HCl solution. -- Abstract: The aim of this study is to explore two different tungsten carbide binders (Co and Ni–Fe) and then impose various sintering temperature treatments. Experimental results show that the optimal sintering temperatures for WC–Co and WC–Ni–Fe hard metal alloys are 1350 °C and 1400 °C for 1 h, respectively. Meanwhile, the WC–Co and WC–Ni–Fe alloys undergo a well liquid-phase sintering and, thus, exhibit excellent mechanical properties. In addition, the sintered WC–Co and WC–Ni–Fe alloys show that when the relative density reached 99.76% and 99.68%, the hardness was enhanced to HRA 84.4 ± 0.5 and 85.3 ± 0.5, and the TRS increased to 2471.2 ± 1.0 and 2524.5 ± 1.0 MPa, respectively. Moreover, the corrosion test results show that the WC–Ni–Fe alloy sintered at 1400 °C had the lowest corrosion current (I corr ) of 1.11 × 10 −5 A cm −2 and the highest polarization resistance (R p ) of 2464.61 Ω cm 2 in 0.15 M HCl solution. Simultaneously, the fracture toughness of K IC increased to 15.1 MPa m 1/2 . Compared with sintered WC–Co alloys, the sintered WC–Ni–Fe hard metal alloys possessed much better corrosion resistance and mechanical properties

  6. Characterization and properties of sintered WC–Co and WC–Ni–Fe hard metal alloys

    Energy Technology Data Exchange (ETDEWEB)

    Chang, Shih-Hsien, E-mail: changsh@ntut.edu.tw; Chen, Song-Ling

    2014-02-05

    Highlights: • WC–Ni–Fe alloy sintered at 1400 °C had the highest hardness (HRA 85.3 ± 0.5). • The optimal WC–Ni–Fe sintered alloy possessed the highest TRS value (2524.5 ± 1.0 MPa). • The fracture toughness of the sintered WC–Ni–Fe alloys is mainly provided by the Ni–Fe binders. • WC–Ni–Fe sintered alloy possessed the highest fracture toughness of K{sub IC} (15.1 MPa m{sup 1/2}). • The WC–Ni–Fe sintered alloy had the much better corrosion resistance in 0.15 M HCl solution. -- Abstract: The aim of this study is to explore two different tungsten carbide binders (Co and Ni–Fe) and then impose various sintering temperature treatments. Experimental results show that the optimal sintering temperatures for WC–Co and WC–Ni–Fe hard metal alloys are 1350 °C and 1400 °C for 1 h, respectively. Meanwhile, the WC–Co and WC–Ni–Fe alloys undergo a well liquid-phase sintering and, thus, exhibit excellent mechanical properties. In addition, the sintered WC–Co and WC–Ni–Fe alloys show that when the relative density reached 99.76% and 99.68%, the hardness was enhanced to HRA 84.4 ± 0.5 and 85.3 ± 0.5, and the TRS increased to 2471.2 ± 1.0 and 2524.5 ± 1.0 MPa, respectively. Moreover, the corrosion test results show that the WC–Ni–Fe alloy sintered at 1400 °C had the lowest corrosion current (I{sub corr}) of 1.11 × 10{sup −5} A cm{sup −2} and the highest polarization resistance (R{sub p}) of 2464.61 Ω cm{sup 2} in 0.15 M HCl solution. Simultaneously, the fracture toughness of K{sub IC} increased to 15.1 MPa m{sup 1/2}. Compared with sintered WC–Co alloys, the sintered WC–Ni–Fe hard metal alloys possessed much better corrosion resistance and mechanical properties.

  7. Tracking the Magnetization Evolution in γ-Fe2O3 / Metallic Fe Core-Shell Nanoparticle Variants

    Science.gov (United States)

    Kons, C.; Nemati, Z.; Srikanth, H.; Phan, M.-H.; Krycka, K.; Borchers, J.; Keavney, D.; Arena, D. A.

    Iron-core magnetic nanoparticles (MNPs) with oxide shells exhibit varying magnetic properties due to the different ordering temperatures of the core and shell spins, as well as the coupling across the metal/oxide interface. While spin coupling across two dimensional interfaces has been well explored, less is known about three dimensional interfaces such as those presented in the MNPs. In this work, MNPs were synthesized with a bcc Fe core and γ-Fe2O3 shell and placed in an oxygen rich environment to encourage the transition from cores shell (CS) to core void shell (CVS) to hollow (H) structures. Static magnetic measurements (MvT) and AC magnetometry were performed to explore the magnetic behavior of the various synthesized structures. To further understand the nature of the spin coupling in the MNPs, TEM and conventional magnetometry as well as variable-temperature small angle neutron scattering (SANS), x-ray absorption spectroscopy (XAS) and x-ray magnetic circular dichroism (XMCD) spectroscopy were performed. Modeling of the x-ray spectra and SANS data will enable us to develop a cohesive picture of spin coupling, freezing and frustration along the three-dimensional metal / oxide interface. Supported by Department of Energy award #DE-FG02-07ER46438; NSF Award #DMR-1508249.

  8. In Silico Switch from Second- to First-Row Transition Metals in Olefin Metathesis: From Ru to Fe and from Rh to Co

    Directory of Open Access Journals (Sweden)

    Jesús Antonio Luque-Urrutia

    2017-12-01

    Full Text Available Density functional theory (DFT calculations have been used to investigate the behavior of different transition metals from Groups 8 (Fe and Ru and 9 (Co and Rh in an already well-known catalytic mechanism, which is based on an Ru(SIMes(PPh3Cl2=CH(Ph complex. As expected, Ru has proven to perform better than their Fe, Co, and Rh counterparts. Even though the topographic steric maps analysis shows no difference in sterical hindrance for any of the metal centers, geometrically, the Fe-based species show a high rigidity with shorter and stronger bonds confirmed by Mayer Bond Orders. The systems bearing Co as a metallic center might present a reactivity that is, surprisingly, too high according to conceptual DFT, which would consequently be a drawback for the formation of the fundamental species of the reaction pathway: the metallacycle intermediate.

  9. Injection-Molded Soft Magnets Prepared from Fe-Based Metallic Glass: Mechanical and Magnetic Properties

    Science.gov (United States)

    Zhong, Tian; Huang, Ran; Huang, Jia; Ouyang, Wei

    2015-10-01

    The injection-molded metallic glass soft magnet is prepared from the powder of melt-spun ribbon of Fe36Co36B20Si4Nb4 glassy alloy and Nylon 6,6 of wt.% from 5 to 20 via the polymer injection molding technology. The product is characterized by the SEM, mechanical, and magnetic test. The results indicate that this type of materials has comparable mechanical properties and morphological feature with the conventional injection-molded NdFeB magnet and exhibits excellent soft magnetic behaviors. The magnetic properties of the injected magnets are compared with the raw metallic glass, solvent-casted resin bonding magnets, and thermal-treated magnets to confirm that the processing temperature of Nylon injection does not affect the magnetism. The injection technology is a practical processing method to be applied on the metallic glass for potential usage.

  10. Critical Evaluation and Thermodynamic Optimization of the Na2O-FeO-Fe2O3-SiO2 System

    Science.gov (United States)

    Moosavi-Khoonsari, Elmira; Jung, In-Ho

    2016-02-01

    A complete literature review, critical evaluation, and thermodynamic optimization of phase diagrams and thermodynamic properties of the Na2O-FeO-Fe2O3-SiO2 system were performed at 1 atm total pressure. A set of optimized model parameters obtained for all phases present in this system reproduces available and reliable thermodynamic properties and phase equilibria within experimental error limits from 298 K (25 °C) to above liquidus temperatures for all compositions and oxygen partial pressures from metallic Fe saturation to 1 atm. The liquid phase was modeled based on the Modified Quasichemical Model considering the possible formation of NaFeO2 associate in the liquid state. The NaFeO2 metaoxide solid solutions containing the excess SiO2 were described within the framework of Compound Energy Formalism. Based on the thermodynamic models and model parameters, unexplored thermodynamic properties and phase diagrams of the Na2O-FeO-Fe2O3-SiO2 system were predicted.

  11. Short-range order in Fe-based metallic glasses: Wide-angle X-ray scattering studies

    International Nuclear Information System (INIS)

    Babilas, Rafał; Hawełek, Łukasz; Burian, Andrzej

    2014-01-01

    The local atomic structure of the Fe 80 B 20 , Fe 70 Nb 10 B 20 and Fe 62 Nb 8 B 30 glasses prepared in the form of ribbons has been studied by wide-angle X-ray scattering. Structural information about the amorphous ribbons has been derived from analysis of the radial distribution functions using the least-squares curve-fitting method. The obtained structural parameters indicate that Fe–Fe, Fe–B, Fe–Nb and Nb–B contributions are involved in the near-neighbor coordination spheres. The possible similarities of the local atomic arrangement in the investigated glasses and the crystalline Fe 3 B, Fe 23 B 6 and bcc Fe structures are also discussed. - Graphical abstract: Pair distribution functions (a) and best-fit model and experimental radial distribution functions for Fe 80 B 20 (b), Fe 70 Nb 10 B 20 (c) and Fe 62 Nb 8 B 30 (d) metallic glasses. - Highlights: • The short-range ordering in the Fe-based metallic glasses is presented. • The results of RDF function have been analyzed using the least-squares method. • The Fe–Fe, Fe–B, Fe–Nb or Nb–B contributions are involved in coordination spheres. • The structural unit is distorted triangular prism containing B, Fe or Nb atoms. • Similarities of atomic arrangement in glassy and crystalline structures are discussed

  12. FeNbB bulk metallic glass with high boron content

    Energy Technology Data Exchange (ETDEWEB)

    Stoica, M.; Das, Jayanta; Eckert, Juergen [IFW Dresden, Institute for Complex Materials, P.O. Box 270016, D-01171 Dresden (Germany); Hajlaoui, Khalil; Yavari, Alain Reza [LTPCM-CNRS, I.N.P. Grenoble, 1130 Rue de la Piscine, BP 75, F-38402 University Campus (France)

    2007-07-01

    Fe-based alloys able to form magnetic bulk metallic glasses (BMGs) are of the type transition metal - metalloid and often contain 5 or more elements. Usually, the metalloid content is around 20 atomic %. Very recently, the Fe{sub 66}Nb{sub 4}B{sub 30} alloy was found to be able to form BMG by copper mold casting technique, despite its high metalloid content. Several composition with boron contents around 30 at. % or even higher were calculated since 1993 as possible compositions of the remaining amorphous matrix after the first stage of nanocrystallization of Finemet-type Fe{sub 77}Si{sub 14}B{sub 9} glassy ribbons with 0.5 to 1 atomic % Cu and a few percent Nb addition. Melt-spun ribbons of all calculated compositions were found to be glassy. The composition of the ternary Fe-based BMG investigated in the present study resulted as an optimization of all possibilities. The alloy is ferromagnetic with glass transition temperature T{sub g}=845 K, crystallisation temperature T{sub x}=876 K, liquidus temperature T{sub liq}=1451 K and mechanical strength of 4 GPa. The coercivity of as-cast samples is very low, around 1.5 A/m. The present contribution aims at discussing the thermal stability, mechanical and magnetic properties of the Fe{sub 66}Nb{sub 4}B{sub 30} BMG.

  13. Phase equilibria and thermodynamic properties of oxide systems on the basis of rare earth, alkaline earth and 3d-transition (Mn, Fe, Co metals. A short overview of

    Directory of Open Access Journals (Sweden)

    V. A. Cherepanov

    2015-12-01

    Full Text Available Review is dedicated studies of phase equilibria in the systems based on rare earth elements and 3d transition metals. It’s highlighted several structural families of these compounds and is shown that many were found interesting properties for practical application, such as high conductivity up to the superconducting state, magnetic properties, catalytic activity of the processes of afterburning of exhaust gases, the high mobility in the oxygen sublattice and more.

  14. Effects of sulfate on heavy metal release from iron corrosion scales in drinking water distribution system.

    Science.gov (United States)

    Sun, Huifang; Shi, Baoyou; Yang, Fan; Wang, Dongsheng

    2017-05-01

    Trace heavy metals accumulated in iron corrosion scales within a drinking water distribution system (DWDS) could potentially be released to bulk water and consequently deteriorate the tap water quality. The objective of this study was to identify and evaluate the release of trace heavy metals in DWDS under changing source water conditions. Experimental pipe loops with different iron corrosion scales were set up to simulate the actual DWDS. The effects of sulfate levels on heavy metal release were systemically investigated. Heavy metal releases of Mn, Ni, Cu, Pb, Cr and As could be rapidly triggered by sulfate addition but the releases slowly decreased over time. Heavy metal release was more severe in pipes transporting groundwater (GW) than in pipes transporting surface water (SW). There were strong positive correlations (R 2  > 0.8) between the releases of Fe and Mn, Fe and Ni, Fe and Cu, and Fe and Pb. When switching to higher sulfate water, iron corrosion scales in all pipe loops tended to be more stable (especially in pipes transporting GW), with a larger proportion of stable constituents (mainly Fe 3 O 4 ) and fewer unstable compounds (β-FeOOH, γ-FeOOH, FeCO 3 and amorphous iron oxides). The main functional iron reducing bacteria (IRB) communities were favorable for the formation of Fe 3 O 4 . The transformation of corrosion scales and the growth of sulfate reducing bacteria (SRB) accounted for the gradually reduced heavy metal release with time. The higher metal release in pipes transporting GW could be due to increased Fe 6 (OH) 12 CO 3 content under higher sulfate concentrations. Copyright © 2017 Elsevier Ltd. All rights reserved.

  15. The effect of different minor additions on the magneto-caloric effect of FeZrB metallic ribbons near room temperature

    Science.gov (United States)

    Guo, D. Q.; Yuan, Y. D.; Chan, K. C.

    2018-01-01

    For room-temperature magnetic refrigerators, magnetocaloric materials are critical for their performance and reliability. Among various magnetocaloric materials, Fe-based metallic glasses, especially in the FeZrB system, have been intensively studied recently due to their promising properties such as low fabrication cost and broad magnetic entropy change peak. In order to further improve the magnetocaloric effect (MCE), the influence of minor additions of Co, Er, Sm and Mn on the MCE of FeZrB-based metallic glasses was systematically investigated in this work. The composition-dependent Curie temperatures (TC) were studied and the magnetic field-dependent MCE was investigated. In two compositions, Fe88Zr7B3Co2 and Fe86Zr8B4Sm2, it was found that their Curie temperatures were close to room temperature and the values of the refrigerant capacity and peak magnetic entropy change were larger than those reported for Fe-based metallic glass at room temperature.

  16. Spectrophotometric speciation of Fe(II) and Fe(III) using hydrazone-micelle systems and flow injections

    International Nuclear Information System (INIS)

    Khojali, Inas Osman

    1999-04-01

    Two hydrazones were synthesised, namely salicylhyrazone (SH) and trihydroxyacetophenone (THAPH) were synthesised with the objective of developing a method for determining of Fe(II) and Fe(III) in the presence of each other and hence the total iron.those hydrazones were selected so as to combine the ability of phenolic compounds to complex Fe(III) ions and the complexing characteristics of hydrazones. The complexes of Fe(II) S H and Fe(III) S H as well those of Fe(II)-THAPH and Fe(III)-THAPH had shown maximum absorbance at λ=412 nm which was not not modified by presence of micelles i.e. sodium n-dodecyl sulphate (SDS) and n-hexa dodecyl pyridinium bromide. The maximum absorbance for all complexes takes place around a neutral pH. Generally, in addition, of n-hexa dodecylpyridinium bromide to fe(II)-SH and Fe(III)-SH absorbance of the complexes increases with increasing the concentration of the micelle. The effects of the addition of sodium n-dodecyle sulphate (SDS) to Fe(III)-SH is also studied. Generally, increasing the concentration of the micelle decrease the absorbance of the complexes. To study the effect of the presence of Fe(II) and Fe(III) on the determination of each other,mixtures of Fe(II)-SH and Fe(III)-SH are studied. However, the use of ascorbic acid as a reducing reagent for Fe(III) did not produce the needed results but non reducible results, which may be due to the masking effect of ascorbic acid and thus making the metal not available to the ligand. However, conversion of Fe(II) to Fe(III) prior to the determination was avoided as this requires the use of oxidant, which will oxidise the ligand as well. To establish the condition for the maximum absorbance of THAPH complexes, the effect of the base was investigated by using sodium and ammonium hydroxide. Generally, increasing the concentration of the base decreases the abosrbance. as expected, ammonium hydroxide produced positive results than sodium hydroxide. After establishing the optimum Fi

  17. Pressure dependence on the remanent magnetization of Fe-Ni alloys and Ni metal

    Science.gov (United States)

    Wei, Qingguo; Gilder, Stuart Alan; Maier, Bernd

    2014-10-01

    We measured the acquisition of magnetic remanence of iron-nickel alloys (Fe64Ni36, Fe58Ni42, and Fe50Ni50) and pure Ni under pressures up to 23 GPa at room temperature. Magnetization decreases markedly for Fe64Ni36 between 5 and 7 GPa yet remains ferromagnetic until at least 16 GPa. Magnetization rises by a factor of 2-3 for the other compositions during compression to the highest applied pressures. Immediately upon decompression, magnetic remanence increases for all Fe-Ni alloys while magnetic coercivity remains fairly constant at relatively low values (5-20 mT). The amount of magnetization gained upon complete decompression correlates with the maximum pressure experienced by the sample. Martensitic effects best explain the increase in remanence rather than grain-size reduction, as the creation of single domain sized grains would raise the coercivity. The magnetic remanence of low Ni Invar alloys increases faster with pressure than for other body-centered-cubic compositions due to the higher magnetostriction of the low Ni Invar metals. Thermal demagnetization spectra of Fe64Ni36 measured after pressure release broaden as a function of peak pressure, with a systematic decrease in Curie temperature. Irreversible strain accumulation from the martensitic transition likely explains the broadening of the Curie temperature spectra, consistent with our x-ray diffraction analyses.

  18. Origin of interfacial perpendicular magnetic anisotropy in MgO/CoFe/metallic capping layer structures

    Science.gov (United States)

    Peng, Shouzhong; Wang, Mengxing; Yang, Hongxin; Zeng, Lang; Nan, Jiang; Zhou, Jiaqi; Zhang, Youguang; Hallal, Ali; Chshiev, Mairbek; Wang, Kang L.; Zhang, Qianfan; Zhao, Weisheng

    2015-12-01

    Spin-transfer-torque magnetic random access memory (STT-MRAM) attracts extensive attentions due to its non-volatility, high density and low power consumption. The core device in STT-MRAM is CoFeB/MgO-based magnetic tunnel junction (MTJ), which possesses a high tunnel magnetoresistance ratio as well as a large value of perpendicular magnetic anisotropy (PMA). It has been experimentally proven that a capping layer coating on CoFeB layer is essential to obtain a strong PMA. However, the physical mechanism of such effect remains unclear. In this paper, we investigate the origin of the PMA in MgO/CoFe/metallic capping layer structures by using a first-principles computation scheme. The trend of PMA variation with different capping materials agrees well with experimental results. We find that interfacial PMA in the three-layer structures comes from both the MgO/CoFe and CoFe/capping layer interfaces, which can be analyzed separately. Furthermore, the PMAs in the CoFe/capping layer interfaces are analyzed through resolving the magnetic anisotropy energy by layer and orbital. The variation of PMA with different capping materials is attributed to the different hybridizations of both d and p orbitals via spin-orbit coupling. This work can significantly benefit the research and development of nanoscale STT-MRAM.

  19. THE ORIGIN OF LOW [α/Fe] RATIOS IN EXTREMELY METAL-POOR STARS

    Energy Technology Data Exchange (ETDEWEB)

    Kobayashi, Chiaki [School of Physics, Astronomy and Mathematics, Centre for Astrophysics Research, University of Hertfordshire, College Lane, Hatfield AL10 9AB (United Kingdom); Ishigaki, Miho N.; Tominaga, Nozomu; Nomoto, Ken' ichi, E-mail: c.kobayashi@herts.ac.uk [Kavli Institute for the Physics and Mathematics of the Universe (WPI), The University of Tokyo, Kashiwa, Chiba 277-8583 (Japan)

    2014-04-10

    We show that the low ratios of α elements (Mg, Si, and Ca) to Fe recently found for a small fraction of extremely metal-poor stars can be naturally explained with the nucleosynthesis yields of core-collapse supernovae, i.e., 13-25 M {sub ☉} supernovae, or hypernovae. For the case without carbon enhancement, the ejected iron mass is normal, consistent with observed light curves and spectra of nearby supernovae. On the other hand, the carbon enhancement requires much smaller iron production, and the low [α/Fe] of carbon-enhanced metal-poor stars can also be reproduced with 13-25 M {sub ☉} faint supernovae or faint hypernovae. Iron-peak element abundances, in particular Zn abundances, are important to put further constraints on the enrichment sources from galactic archaeology surveys.

  20. Moessbauer-spectroscopic study of structure and magnetism of the exchange-coupled layer systems Fe/FeSn{sub 2}, and Fe/FeSi/Si and the ion-implanted diluted magnetic semiconductor SiC(Fe); Moessbauerspektroskopische Untersuchung von Struktur und Magnetismus der austauschgekoppelten Schichtsysteme Fe/FeSn{sub 2} und Fe/FeSi/Si und des ionenimplantierten verduennten magnetischen Halbleiters SiC(Fe)

    Energy Technology Data Exchange (ETDEWEB)

    Stromberg, Frank

    2009-07-07

    In line with this work the structural and magnetic properties of the exchange coupled layered systems Fe/FeSn{sub 2} and Fe/FeSi/Si and of the Fe ion implanted diluted magnetic semiconductor (DMS) SiC(Fe) were investigated. The main measuring method was the isotope selective {sup 57}Fe conversion electron Moessbauer spectroscopy (CEMS), mostly in connection with the {sup 57}Fe tracer layer technique, in a temperature range from 4.2 K to 340 K. Further measurement techniques were X-ray diffraction (XRD), electron diffraction (LEED, RHEED), SQUID magnetometry and FMR (Ferromagnetic Resonance). In the first part of this work the properties of thin AF FeSn{sub 2}(001) films and of the exchange-bias system Fe/FeSn{sub 2}(001) on InSb(001) were investigated. With the application of {sup 57}Fe-tracer layers and CEMS both the Fe-spin structure and the temperature dependence of the magnetic hyperfine field (B{sub hf}) of FeSn{sub 2} could be examined. The evaporation of Fe films on the FeSn{sub 2} films produced in the latter ones a high perpendicular spin component at the Fe/FeSn{sub 2} interface. In some distance from the interface the Fe spins rotate back into the sample plane. Furthermore {sup 57}Fe-CEMS provided a correlation between the absolute value of the exchange field vertical stroke He vertical stroke and the amount of magnetic defects within the FeSn{sub 2}. Temperature dependent CEMS-measurements yielded informations about the spin dynamics within the AF. The transition temperatures T{sub B}{sup *}, which were interpreted as superparamagnetic blocking temperatures, obtain higher values compared to the temperatures T{sub B} of the exchange-bias effect, obtained with magnetometry measurements. The second part of this work deals with the indirect exchange coupling within Fe/FeSi/Si/FeSi/Fe multilayers and FeSi diffusion barriers. The goal was to achieve Fe free Si interlayers. The CEMS results show that starting from a thickness of t{sub FeSi}=10-12 A of the

  1. Exploring the Photovoltaic Properties of Metal Bipyridine Complexes (Metal = Fe, Zn, Cr, and Ru) by Density Functional Theory

    Science.gov (United States)

    Irfan, Ahmad; Abbas, Ghulam

    2018-03-01

    The synthesis and characterisation of mononuclear Fe complexes were carried out by using bipyridine (Compound 1) at ambient conditions. Additionally, three more derivatives were designed by substituting the central Fe metal with Zn, Cr, and Ru (Compound 2, Compound 3, and Compound 4), respectively. The ground state geometry calculations were carried out by using density functional theory (DFT) at B3LYP/6-31G** (LANL2DZ) level of theory. We shed light on the frontier molecular orbitals, electronic properties, photovoltaic parameters, and structure-property relationship. The open-circuit voltage is a promising parameter that considerably affects the photovoltaic performance; thus, we have estimated its value by considering the complexes as donors whereas TiO2 and/or Si were used as acceptors. The solar cell performance behaviour was also studied by shedding light on the band alignment and energy level offset.

  2. Ethylene Epoxidation with Nitrous Oxide over Fe-BTC Metal-Organic Frameworks: A DFT Study.

    Science.gov (United States)

    Maihom, Thana; Choomwattana, Saowapak; Wannakao, Sippakorn; Probst, Michael; Limtrakul, Jumras

    2016-11-04

    The epoxidation of ethylene with N 2 O over the metal-organic framework Fe-BTC (BTC=1,3,5-benzentricarboxylate) is investigated by means of density functional calculations. Two reaction paths for the production of ethylene oxide or acetaldehyde are systematically considered in order to assess the efficiency of Fe-BTC for the selective formation of ethylene oxide. The reaction starts with the decomposition of N 2 O to form an active surface oxygen atom on the Fe site of Fe-BTC, which subsequently reacts with an ethylene molecule to form an ethyleneoxy intermediate. This intermediate can then be selectively transformed either by 1,2-hydride shift into the undesired product acetaldehyde or into the desired product ethylene oxide by way of ring closure of the intermediate. The production of ethylene oxide requires an activation energy of 5.1 kcal mol -1 , which is only about one-third of the activation energy of acetaldehyde formation (14.3 kcal mol -1 ). The predicted reaction rate constants for the formation of ethylene oxide in the relevant temperature range are approximately 2-4 orders of magnitude higher than those for acetaldehyde. Altogether, the results suggest that Fe-BTC is a good candidate catalyst for the epoxidation of ethylene by molecular N 2 O. © 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  3. Thermoplastic deformation of ferromagnetic CoFe-based bulk metallic glasses

    Science.gov (United States)

    Wu, Chenguang; Hu, Renchao; Man, Qikui; Chang, Chuntao; Wang, Xinmin

    2017-12-01

    The superplastic deformation behavior of the ferromagnetic Co31Fe31Nb8B30 bulk metallic glass (BMG) in the supercooled liquid region was investigated. At a given temperature, the BMG exhibits a Newtonian behavior at low strain rates but a non-Newtonian behavior at high strain rates. The high thermal stability of this glassy alloy system offers an enough processing window to thermoplastic forming (TPF), and the strong processing ability was examined by simple micro-replication experiments. It is demonstrated that the TPF formability on length scales ranging down to nanometers can be achieved in the selected experimental condition. Based on the analysis of deformation behavior, the nearly full density sample (i.e. nearly 100%), was produced from water-atomized glassy powders and consolidated by the hot-pressing technique. The sample exhibits good soft-magnetic and mechanical properties, i.e., low coercive force of 0.43 Oe, high initial permeability of 4100 and high Vickers hardness 1398. These results suggest that the hot-pressing process opens up possibilities for the commercial exploitation of BMGs in engineering applications.

  4. MWCNTs/metal (Ni, Co, Fe) oxide nanocomposite as potential material for supercapacitors application in acidic and neutral media

    CSIR Research Space (South Africa)

    Adekunle, AS

    2013-05-01

    Full Text Available Supercapacitive properties of synthesised metal oxides nanoparticles (MO where M = Ni, Co, Fe) integrated with multi-wall carbon nanotubes (MWCNT) on basal plane pyrolytic graphite electrode (BPPGE) were investigated. Successful modification...

  5. Regulation of brain copper homeostasis by the brain barrier systems: Effects of Fe-overload and Fe-deficiency

    Energy Technology Data Exchange (ETDEWEB)

    Monnot, Andrew D.; Behl, Mamta; Ho, Sanna; Zheng, Wei, E-mail: wzheng@purdue.edu

    2011-11-15

    Maintaining brain Cu homeostasis is vital for normal brain function. The role of systemic Fe deficiency (FeD) or overload (FeO) due to metabolic diseases or environmental insults in Cu homeostasis in the cerebrospinal fluid (CSF) and brain tissues remains unknown. This study was designed to investigate how blood-brain barrier (BBB) and blood-SCF barrier (BCB) regulated Cu transport and how FeO or FeD altered brain Cu homeostasis. Rats received an Fe-enriched or Fe-depleted diet for 4 weeks. FeD and FeO treatment resulted in a significant increase (+ 55%) and decrease (- 56%) in CSF Cu levels (p < 0.05), respectively; however, neither treatment had any effect on CSF Fe levels. The FeD, but not FeO, led to significant increases in Cu levels in brain parenchyma and the choroid plexus. In situ brain perfusion studies demonstrated that the rate of Cu transport into the brain parenchyma was significantly faster in FeD rats (+ 92%) and significantly slower (- 53%) in FeO rats than in controls. In vitro two chamber Transwell transepithelial transport studies using primary choroidal epithelial cells revealed a predominant efflux of Cu from the CSF to blood compartment by the BCB. Further ventriculo-cisternal perfusion studies showed that Cu clearance by the choroid plexus in FeD animals was significantly greater than control (p < 0.05). Taken together, our results demonstrate that both the BBB and BCB contribute to maintain a stable Cu homeostasis in the brain and CSF. Cu appears to enter the brain primarily via the BBB and is subsequently removed from the CSF by the BCB. FeD has a more profound effect on brain Cu levels than FeO. FeD increases Cu transport at the brain barriers and prompts Cu overload in the CNS. The BCB plays a key role in removing the excess Cu from the CSF.

  6. Temperature-induced delocalization of charge carriers and semiconductor to metal-like phase in SrFeO{sub 3-δ}

    Energy Technology Data Exchange (ETDEWEB)

    Manimuthu, P.; Venkateswaran, C. [University of Madras, Department of Nuclear Physics, Guindy Campus, Chennai (India); Murugaraj, R. [Anna University, Department of Physics, MIT Campus, Chennai (India)

    2015-04-01

    Perovskite SrFeO{sub 3-δ}, a Ruddlesden-Popper class of system exhibits interesting electronic and magnetic properties. Influence of oxygen vacancies on the electrical response of nanocrystalline SrFeO{sub 2.91} as a function of temperature is investigated using impedance spectroscopy technique. A change observed in the Nyquist plot at 383 K has been analyzed in terms of localized and delocalized e{sub g} electrons. An unusual and interesting temperature-induced semiconductor to metal-like transition is observed in the frequency-dependent real part of dielectric permittivity. Dependence of frequency on the real and imaginary parts of impedance with respect to temperature supports the presence of semiconductor to metal-like transition in SrFeO{sub 2.91}. (orig.)

  7. Advances in metal forming expert system for metal forming

    CERN Document Server

    Hingole, Rahulkumar Shivajirao

    2015-01-01

    This comprehensive book offers a clear account of the theory and applications of advanced metal forming. It provides a detailed discussion of specific forming processes, such as deep drawing, rolling, bending extrusion and stamping. The author highlights recent developments of metal forming technologies and explains sound, new and powerful expert system techniques for solving advanced engineering problems in metal forming. In addition, the basics of expert systems, their importance and applications to metal forming processes, computer-aided analysis of metalworking processes, formability analysis, mathematical modeling and case studies of individual processes are presented.

  8. Fabrication and characterization of nanostructured Fe{sub 3}S{sub 4}, an isostructural compound of half-metallic Fe{sub 3}O{sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Li, Peng [Division of Physical Science and Engineering, King Abdullah University of Science and Technology (KAUST), Thuwal 23955 (Saudi Arabia); Tianjin Key Laboratory of Low Dimensional Materials Physics and Preparing Technology, Faculty of Science, Institute of Advanced Materials Physics, Tianjin University, Tianjin 300072 (China); Xia, Chuan; Zhang, Qiang; Alshareef, Husam N.; Zhang, Xi-xiang, E-mail: xixiang.zhang@kaust.edu.sa [Division of Physical Science and Engineering, King Abdullah University of Science and Technology (KAUST), Thuwal 23955 (Saudi Arabia); Guo, Zaibing [Advanced Nanofabrication, Imaging and Characterization Core Lab, King Abdullah University of Science and Technology, Thuwal-239955 (Saudi Arabia); Cui, Wenyao; Bai, Haili [Tianjin Key Laboratory of Low Dimensional Materials Physics and Preparing Technology, Faculty of Science, Institute of Advanced Materials Physics, Tianjin University, Tianjin 300072 (China)

    2015-06-14

    High-purity, well-crystallized spinel Fe{sub 3}S{sub 4} nanoplatelets were synthesized by the hydrothermal method, and the saturation magnetic moment of Fe{sub 3}S{sub 4} was measured at 1.83 μ{sub B}/f.u. The temperature-dependent resistivity of Fe{sub 3}S{sub 4} was metallic-like for T < 180 K: room-temperature resistivity was measured at 7.711 × 10{sup 3 }μΩ cm. The anomalous Hall conductivity of Fe{sub 3}S{sub 4} decreased with increasing longitudinal conductivity, in sharp contrast with the accepted theory of the anomalous Hall effect in a dirty-metal regime. Furthermore, negligible spin-dependent magnetoresistance was observed. Band structure calculations confirmed our experimental observations that Fe{sub 3}S{sub 4} is a metal and not a half metal as expected.

  9. Combined effects of ultrasonic vibration and manganese on Fe-containing inter-metallic compounds and mechanical properties of Al-17Si alloy with 3wt.%Fe

    Directory of Open Access Journals (Sweden)

    Lin Chong

    2013-05-01

    Full Text Available The research studied the combined effects of ultrasonic vibration (USV and manganese on the Fe-containing inter-metallic compounds and mechanical properties of Al-17Si-3Fe-2Cu-1Ni (wt.% alloys. The results showed that, without USV, the alloys with 0.4wt.% Mn or 0.8wt.% Mn both contain a large amount of coarse plate-like δ-Al4(Fe,MnSi2 phase and long needle-like β-Al5(Fe,MnSi phase. When the Mn content changes from 0.4wt.% to 0.8wt.% in the alloys, the amount and the length of needle-like β-Al5(Fe,MnSi phase decrease and the plate-like δ-Al4(Fe,MnSi2 phase becomes much coarser. After USV treatment, the Fe-containing compounds in the alloys are refined and exist mainly as δ-Al4(Fe,MnSi2 particles with an average grain size of about 20 μm, and only a small amount of β-Al5(Fe,MnSi phase remains. With USV treatment, the ultimate tensile strengths (UTS of the alloys containing 0.4wt.%Mn and 0.8wt.%Mn at room temperature are 253 MPa and 262 MPa, respectively, and the ultimate tensile strengths at 350 °C are 129 MPa and 135 MPa, respectively. It is considered that the modified morphology and uniform distribution of the Fe-containing inter-metallic compounds, which are caused by the USV process, are the main reasons for the increase in the tensile strength of these two alloys.

  10. Fe(III)-based metal-organic framework-derived core-shell nanostructure: Sensitive electrochemical platform for high trace determination of heavy metal ions.

    Science.gov (United States)

    Zhang, Zhihong; Ji, Hongfei; Song, Yingpan; Zhang, Shuai; Wang, Minghua; Jia, Changchang; Tian, Jia-Yue; He, Linghao; Zhang, Xiaojing; Liu, Chun-Sen

    2017-08-15

    A new core-shell nanostructured composite composed of Fe(III)-based metal-organic framework (Fe-MOF) and mesoporous Fe 3 O 4 @C nanocapsules (denoted as Fe-MOF@mFe 3 O 4 @mC) was synthesized and developed as a platform for determining trace heavy metal ions in aqueous solution. Herein, the mFe 3 O 4 @mC nanocapsules were prepared by calcining the hollow Fe 3 O 4 @C that was obtained using the SiO 2 nanoparticles as the template, followed by composing the Fe-MOF. The Fe-MOF@mFe 3 O 4 @mC nanocomposite demonstrated excellent electrochemical activity, water stability and high specific surface area, consequently resulting in the strong biobinding with heavy-metal-ion-targeted aptamer strands. Furthermore, by combining the conformational transition interaction, which is caused by the formation of the G-quadruplex between a single-stranded aptamer and high adsorbed amounts of heavy metal ions, the developed aptasensor exhibited a good linear relationship with the logarithm of heavy metal ion (Pb 2+ and As 3+ ) concentration over the broad range from 0.01 to 10.0nM. The detection limits were estimated to be 2.27 and 6.73 pM toward detecting Pb 2+ and As 3+ , respectively. The proposed aptasensor showed good regenerability, excellent selectivity, and acceptable reproducibility, suggesting promising applications in environment monitoring and biomedical fields. Copyright © 2017 Elsevier B.V. All rights reserved.

  11. The system Fe-Nb-S and its geological implications

    Czech Academy of Sciences Publication Activity Database

    Drábek, M.; Hybler, Jiří; Rieder, M.; Böhmová, Vlasta

    2010-01-01

    Roč. 48, č. 5 (2010), s. 1059-1068 ISSN 0008-4476 R&D Projects: GA ČR GA205/08/0122 Institutional research plan: CEZ:AV0Z10100521; CEZ:AV0Z30130516 Keywords : phase relations * edgarite * Fe x Nb y S 2 solid solution * Nb sulfides * system Fe-Nb-S * crystal-structure refinements Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 1.289, year: 2010

  12. Regulation of brain copper homeostasis by the brain barrier systems: effects of Fe-overload and Fe-deficiency.

    Science.gov (United States)

    Monnot, Andrew D; Behl, Mamta; Ho, Sanna; Zheng, Wei

    2011-11-01

    Maintaining brain Cu homeostasis is vital for normal brain function. The role of systemic Fe deficiency (FeD) or overload (FeO) due to metabolic diseases or environmental insults in Cu homeostasis in the cerebrospinal fluid (CSF) and brain tissues remains unknown. This study was designed to investigate how blood-brain barrier (BBB) and blood-SCF barrier (BCB) regulated Cu transport and how FeO or FeD altered brain Cu homeostasis. Rats received an Fe-enriched or Fe-depleted diet for 4 weeks. FeD and FeO treatment resulted in a significant increase (+55%) and decrease (-56%) in CSF Cu levels (pBCB. Further ventriculo-cisternal perfusion studies showed that Cu clearance by the choroid plexus in FeD animals was significantly greater than control (pBCB contribute to maintain a stable Cu homeostasis in the brain and CSF. Cu appears to enter the brain primarily via the BBB and is subsequently removed from the CSF by the BCB. FeD has a more profound effect on brain Cu levels than FeO. FeD increases Cu transport at the brain barriers and prompts Cu overload in the CNS. The BCB plays a key role in removing the excess Cu from the CSF. Copyright © 2011 Elsevier Inc. All rights reserved.

  13. Impact of biogenic nanoscale metals Fe, Cu, Zn and Se on reproductive LV chickens

    International Nuclear Information System (INIS)

    Nguyen, Quy Khiem; Nguyen, Van Kien; Nguyen, Khac Thinh; Nguyen, Duy Dieu; Nguyen, Hoai Chau; Tran, Xuan Tin; Nguyen, Huu Cuong; Phung, Duc Tien

    2015-01-01

    Using biogenic nanoscale metals (Fe, Cu, ZnO, Se) to supplement into diet premix of reproductive LV (a Vietnamese Luong Phuong chicken breed) chickens resulted in certain improvement of poultry farming. The experimental data obtained showed that the farming indices depend mainly on the quantity of nanocrystalline metals which replaced the inorganic mineral component in the feed premix. All four experimental groups with different quantities of the replacement nano component grew and developed normally with livability reaching 91 to 94%, hen’s bodyweight at 38 weeks of age and egg weight ranged from 2.53–2.60 kg/hen and 50.86–51.55 g/egg, respectively. All these farming indices together with laying rate, egg productivity and chick hatchability peaked at group 5 with 25% of nanoscale metals compared to the standard inorganic mineral supplement, while feed consumption was lowest. The results also confirmed that nanocrystalline metals Fe, Cu, ZnO and Se supplemented to chicken feed were able to decrease inorganic minerals in the diet premixes at least four times, allowing animals to more effectively absorb feed minerals, consequently decreasing environmental pollution risks. (paper)

  14. Hard magnetic properties and coercivity mechanism of melt-spun Misch Metal-Fe-B alloy

    Energy Technology Data Exchange (ETDEWEB)

    Quan, Ningtao; Luo, Yang, E-mail: eluoyang@foxmail.com; Yan, Wenlong; Yuan, Chao; Yu, Dunbo; Sun, Liang; Lu, Shuo; Li, Hongwei; Zhang, Hongbin

    2017-09-01

    Highlights: • Melt-spun MM{sub 13}Fe{sub 81}B{sub 6} alloy shows that the distributions of the La, Ce, Pr, Nd, Fe and B elements is uniformly distributed, and the grain size is in the range of 30–40 nm, it can be seen that Pr-rich and La-rich phases concentrated on grain boundaries, which resulted in the coercivity augment with the increase of MMFe{sub 2} content, and the grain size is around 40–50 nm in MM{sub 16}Fe{sub 78}B{sub 6}. • There is a significant formation of MMFe{sub 2} with abundant Pr and La, and a small amount of Ce and Nd enriched at the interfacial region in MM{sub 16}Fe{sub 78}B{sub 6}, thus an inhomogeneous region was formed. It is considered that the inhomogeneous region is effective in increasing the coercivity. • The optimum-quenched MM{sub 13}Fe{sub 81}B{sub 6} alloy have been shown to exhibit a coercive force of 6.9 kOe and an energy product of 8.5 MGOe, which is superior to anisotropic ferrite magnets of 4.5 MGOe. - Abstract: Magnetic and structural properties of Misch Metal (MM)-Fe-B alloys, were examined in the melt-spun ribbons. Melt-spun MM-Fe-B samples were prepared at the surface velocities of 18–30 m/s. Crystalline structure and their room-temperature magnetization characteristics were analyzed, and the optimum surface velocity of 20 m/s and nominal composition of MM{sub 13}Fe{sub 81}B{sub 6} were obtained. Microstructural analyses indicate that the grain size is approximately 30–50 nm in the alloys with the optimum characteristics. In the MM{sub 16}Fe{sub 78}B{sub 6} alloys, Pr-rich and La-rich phases concentrated on grain boundaries, which resulted in the coercivity augment with the increase of MMFe{sub 2} content. Dependence of coercivity on applied magnetic field suggested that the mechanism of coercivity in moderate MM-content samples was inhomogeneous domain wall pinning type. The melt-spun ribbons in the optimum condition exhibit a coercive force of 6.9 kOe and an energy product of 8.5 MGOe, which can be used as

  15. Bandstructure calculations for metal hydrogen systems

    International Nuclear Information System (INIS)

    Switendick, A.C.

    1979-01-01

    The factors contributing to hydride stability are discussed for a variety of metal hydride systems. The formation of a low-lying hydrogen associated state is a common feature. A significant transition metal character is also found in these states

  16. Removing metal debris from thermosetting EMC powders by Nd-Fe-B permanent magnets

    Directory of Open Access Journals (Sweden)

    Liaw Yowching

    2017-01-01

    Full Text Available During the preparation of thermosetting encapsulation molding compounds (EMCs for semiconductor packaging, metal debris are always present in the EMC powders due to the hard silica fillers in the compound. These metal debris in the EMC powders will cause circuit shortage and therefore have to be removed before molding. In this study, Nd-Fe-B permanent magnets are used to remove these debris. The results show that the metal debris can be removed effectively as the rate of accumulation of the metal debris increases as time proceeds in the removing operation. The removal effectiveness of the debris is affected by both the magnetic flux density and the flow around the magnet. The wake flow behind the magnet is a relatively low speed recirculation region which facilities the attraction of metal debris in the powders. Thus, the largest amount of the accumulated EMC powders occurs downstream of the magnet. Hence, this low speed recirculation region should be better utilized to enhance the removal efficiency of the metal debris.

  17. Formation and stability of aluminum-based metallic glasses in Al-Fe-Gd alloys

    International Nuclear Information System (INIS)

    He, Y.; Poon, S.J.; Shiflet, G.J.

    1988-01-01

    Metallic glasses, a class of amorphous alloys made by rapid solidification, have been studied quite extensively for almost thirty years. It has been recognized for a long time that metallic glasses are usually very strong and ductile, and exhibit high corrosion resistance relative to crystalline alloys with the same compositions. Recently, metallic glasses containing as much as 90 atomic percent aluminum have been discovered independently by two groups. This discovery has both scientific and technological implications. The formability of these new glasses have been found to be unusual. Studies of mechanical properties in these new metallic glasses show that many of them have tensile strengths over 800MPa, greatly exceeding the strongest commercial aluminum alloys. The high strengths of aluminum-rich metallic glasses can be of significant importance in obtaining high strength low density materials. Therefore, from both scientific and technological standpoints, it is important to understand the formation and thermal stability of these metallic glasses. Al-Fe-Gd alloys were chosen for a more detailed study since they exhibit high tensile strengths

  18. TRACE METAL CONTENT (Cu, Zn, Mn AND Fe) IN URTICA DIOICA L. AND PLANTAGO MAJOR L.

    Science.gov (United States)

    Krolak, Elzbieta; Raczuk, Jolanta; Borkowska, Lidia

    2016-11-01

    The aim of the study was to compare the contents of Cu, Zn, Mn and Fe in the washed and unwashed leaves and roots of two plant species: Urica dioica L. and Plantago major L., used in herbal medicine. These two herb species occur in the same environmental habitats, yet their morphological structure is different. The soil and plant samples for analyses were collected from an uncontaminated area in Eastern Poland. In each habitat location, the samples were taken from sandy soils with slightly acidic and neutral pH values. The obtained results showed that U. dioica and P. major accumulated similar amounts of trace metals, such as: Cu, Zn and Fe, in leaves, despite the differences in the morphological structure of their overground parts. The content of Mn in leaves U. dioica was about twice as much as in P. major. Also, no differences in the metal content were observed between washed and unwashed leaves of both species. However, in the same habitat conditions, a significantly higher content of Cu, Zn and Mn was found in the roots of P. major than U. dioica. The content of Fe in the roots was similar in both species. P. major and U. dioica may be a valuable source of microelements, if they are obtained from unpolluted habitats.

  19. Outstanding resistance and passivation behaviour of new Fe-Co metal-metal glassy alloys in alkaline media.

    Directory of Open Access Journals (Sweden)

    Khadijah M Emran

    Full Text Available The electrochemical behavior of the oxide layers on two metal-metal glassy alloys, Fe78Co9Cr10Mo2Al1 (VX9and Fe49Co49V2 (VX50 (at.%, were studied using electrochemical techniques including electrochemical frequency modulation (EFM, electrochemical impedance spectroscopy (EIS and cyclic polarization (CP measurements. The morphology and composition of the alloy surfaces were investigated using X-ray photoelectron spectroscopy (XPS, scanning electron microscopy (SEM and atomic force microscopy (AFM. The corrosion rate and surface roughness of both alloys increased as the concentration of NaOH in aqueous solution was raised. The presence of some protective elements in the composition of the alloys led to the formation of a spontaneous passive layer on the alloy surface. The higher resistance values of both alloys were associated with the magnitude of the dielectric properties of the passive films formed on their surfaces. Both alloys are classified as having outstanding resistance to corrosion, which results from the formation of a passive film that acts as an efficient barrier to corrosion in alkaline solution.

  20. Outstanding resistance and passivation behaviour of new Fe-Co metal-metal glassy alloys in alkaline media.

    Science.gov (United States)

    Emran, Khadijah M; Al-Harbi, Albandaree K

    2018-01-01

    The electrochemical behavior of the oxide layers on two metal-metal glassy alloys, Fe78Co9Cr10Mo2Al1 (VX9)and Fe49Co49V2 (VX50) (at.%), were studied using electrochemical techniques including electrochemical frequency modulation (EFM), electrochemical impedance spectroscopy (EIS) and cyclic polarization (CP) measurements. The morphology and composition of the alloy surfaces were investigated using X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and atomic force microscopy (AFM). The corrosion rate and surface roughness of both alloys increased as the concentration of NaOH in aqueous solution was raised. The presence of some protective elements in the composition of the alloys led to the formation of a spontaneous passive layer on the alloy surface. The higher resistance values of both alloys were associated with the magnitude of the dielectric properties of the passive films formed on their surfaces. Both alloys are classified as having outstanding resistance to corrosion, which results from the formation of a passive film that acts as an efficient barrier to corrosion in alkaline solution.

  1. Surface preparation of FeS[sub 2] via electrochemical etching and interface formation with metals

    Energy Technology Data Exchange (ETDEWEB)

    Bronold, M. (Abt. Solare Energetik, Hahn-Meitner-Inst. Berlin (Germany)); Bueker, K. (Abt. Solare Energetik, Hahn-Meitner-Inst. Berlin (Germany)); Kubala, S. (Abt. Solare Energetik, Hahn-Meitner-Inst. Berlin (Germany)); Pettenkofer, C. (Abt. Solare Energetik, Hahn-Meitner-Inst. Berlin (Germany)); Tributsch, H. (Abt. Solare Energetik, Hahn-Meitner-Inst. Berlin (Germany))

    1993-01-16

    The effect of passing cathodic currents at potentials of hydrogen evolution through differently pretreated n-type pyrite (FeS[sub 2]) electrodes is studied by XPS. It is shown that hydrogen evolution results in an etching of the crystal via dissolution of FeS[sub 2]. Surfaces that are destroyed through sputtering or polishing are restored through this etching procedure. (100) and (111) surfaces behave similar to each other. When depositing gold onto the electrochemically etched surface in ultrahigh vacuum no change of the band bending of the clean surface (650 meV) is observed. An abrupt interface with FeS-like defects in the pyrite is formed. deposition of platinum yields a ternary Pt-Fe-S interlayer between pyrite and metallic Pt. The band bending is reduced by 200 meV during contact formation. Concerning the chemical composition and the electronic structure the etched surfaces behave nearly identical to clean (100) cleavage planes of pyrite. (orig.)

  2. Co{sub x}Fe{sub (x-1)}S{sub 2}: How close to half-metallicity?

    Energy Technology Data Exchange (ETDEWEB)

    Utfeld, C.; Laverock, J.; Dugdale, S.B. [H.H. Wills Physics Laboratory, University of Bristol, Tyndall Avenue, Bristol BS8 1TL (United Kingdom); Giblin, S.R.; Taylor, J.W. [ISIS Facility, RAL, Chilton, Oxfordshire OX11 0QX (United Kingdom); Shenton-Taylor, C.; Duffy, J.A. [Department of Physics, University of Warwick, Coventry CV4 7AL (United Kingdom); Wang, L.; Leighton, C. [Chem. Eng. and Mat. Sci., University of Minnesota, Minneapolis, MN 55455 (United States); Itou, M.; Sakurai, Y. [SPring-8, 1-1-1 Kouto, Mikazuki, Sayo, Hyogo 679-5198 (Japan)

    2009-07-01

    CoS{sub 2} is a material thought to be very close to being a half-metal, i.e. to only be conducting in one spin. However, the Fermi level lies low in the conduction bands and doping with the isostructural semiconductor FeS{sub 2} is predicted to gradually unoccupy one spin channel. In this context the evolution of the polarisation across the series Co{sub x}Fe{sub (1-x)}S{sub 2} is of major interest. Experimentally the number of direct measurements accessing the bulk polarisation for different alloy compositions is rather limited. We present a magnetic Compton scattering study combined with ab initio calculations as a method to determine the bulk spin polarisation in CoS{sub 2} and Co{sub 0.9}Fe{sub 0.1}S{sub 2}. Magnetic Compton scattering is a versatile technique for investigations into spin-dependent bulk properties because it probes the unpaired electrons directly. We compare the data with theoretical predictions and optimise the agreement by rigidly shifting the bands in order to extract the tuned bulk polarisations of P{approx}-75% and P{approx}18% for the pure and the x=0.1 system, respectively.

  3. Liquid metal MHD generator systems

    International Nuclear Information System (INIS)

    Satyamurthy, P.; Dixit, N.S.; Venkataramani, N.; Rohatgi, V.K.

    1985-01-01

    Liquid Metal MHD (LMMHD) Generator Systems are becoming increasingly important in space and terrestrial applications due to their compactness and versatility. This report gives the current status and economic viability of LMMHD generators coupled to solar collectors, fast breeder reactors, low grade heat sources and conventional high grade heat sources. The various thermodynamic cycles in the temperatures range of 100degC-2000degC have been examined. The report also discusses the present understanding of various loss mechanisms inherent in LMMHD systems and the techniques for overcoming these losses. A small mercury-air LMMHD experimental facility being set up in Plasma Physics Division along with proposals for future development of this new technology is also presented in this report. (author)

  4. Halo Formation During Solidification of Refractory Metal Aluminide Ternary Systems

    Science.gov (United States)

    D'Souza, N.; Feitosa, L. M.; West, G. D.; Dong, H. B.

    2018-02-01

    The evolution of eutectic morphologies following primary solidification has been studied in the refractory metal aluminide (Ta-Al-Fe, Nb-Al-Co, and Nb-Al-Fe) ternary systems. The undercooling accompanying solid growth, as related to the extended solute solubility in the primary and secondary phases can be used to account for the evolution of phase morphologies during ternary eutectic solidification. For small undercooling, the conditions of interfacial equilibrium remain valid, while in the case of significant undercooling when nucleation constraints occur, there is a departure from equilibrium leading to unexpected phases. In Ta-Al-Fe, an extended solubility of Fe in σ was observed, which was consistent with the formation of a halo of μ phase on primary σ. In Nb-Al-Co, a halo of C14 is formed on primary CoAl, but very limited vice versa. However, in the absence of a solidus projection it was not possible to definitively determine the extended solute solubility in the primary phase. In Nb-Al-Fe when nucleation constraints arise, the inability to initiate coupled growth of NbAl3 + C14 leads to the occurrence of a two-phase halo of C14 + Nb2Al, indicating a large undercooling and departure from equilibrium.

  5. Phase equilibria in the Mo-Fe-P system at 800 °C and structure of ternary phosphide (Mo(1-x)Fe(x))3P (0.10 ≤ x ≤ 0.15).

    Science.gov (United States)

    Oliynyk, Anton O; Lomnytska, Yaroslava F; Dzevenko, Mariya V; Stoyko, Stanislav S; Mar, Arthur

    2013-01-18

    Construction of the isothermal section in the metal-rich portion (ternary phases: (Mo(1-x)Fe(x))(2)P (x = 0.30-0.82) and (Mo(1-x)Fe(x))(3)P (x = 0.10-0.15). The occurrence of a Co(2)Si-type ternary phase (Mo(1-x)Fe(x))(2)P, which straddles the equiatomic composition MoFeP, is common to other ternary transition-metal phosphide systems. However, the ternary phase (Mo(1-x)Fe(x))(3)P is unusual because it is distinct from the binary phase Mo(3)P, notwithstanding their similar compositions and structures. The relationship has been clarified through single-crystal X-ray diffraction studies on Mo(3)P (α-V(3)S-type, space group I42m, a = 9.7925(11) Å, c = 4.8246(6) Å) and (Mo(0.85)Fe(0.15))(3)P (Ni(3)P-type, space group I4, a = 9.6982(8) Å, c = 4.7590(4) Å) at -100 °C. Representation in terms of nets containing fused triangles provides a pathway to transform these closely related structures through twisting. Band structure calculations support the adoption of these structure types and the site preference of Fe atoms. Electrical resistivity measurements on (Mo(0.85)Fe(0.15))(3)P reveal metallic behavior but no superconducting transition.

  6. Effects of Cu substitution for Fe on the glass-forming ability and soft magnetic properties for Fe-based bulk metallic glasses

    International Nuclear Information System (INIS)

    Dou, Lintao; Liu, Haishun; Hou, Long; Xue, Lin; Yang, Weiming; Zhao, Yucheng; Chang, Chuntao

    2014-01-01

    The effects of Cu substitution for Fe on the glass-forming ability (GFA) and soft magnetic properties for Fe 72−x Cu x B 20 Si 4 Nb 4 (x=0.0, 0.2, 0.4, 0.6, 0.8, and 1.0) bulk metallic glasses (BMGs) are investigated. It is found that the investigated BMGs exhibit large GFA as well as excellent soft magnetic properties, and proper substitution of Fe by Cu improves the saturation magnetization, coercive force, and effective permeability without obvious deterioration of the GFA. - Highlights: • Fully glassy rods of Fe 72−x Cu x B 20 Si 4 Nb 4 BMGs were produced above 1 mm in diameter. • Investigated BMGs exhibit large glass-forming ability and excellent soft magnetic properties. • Proper Cu substitution improves magnetic properties without obvious deterioration of glass-forming ability

  7. Virtual half-metallicity at the CoS2/FeS2 interface induced by strain

    KAUST Repository

    Nazir, Safdar

    2013-01-01

    Spin polarized ab initio calculations based on density functional theory are performed to investigate the electronic and magnetic properties of the interface between the ferromagnetic metal CoS2 and the nonmagnetic semiconductor FeS2. Relaxation of the interface structure is taken into account by atomic force minimization. We find that both Co and Fe are close to half-metallicity at the interface. Tensile strain is shown to strongly enhance the spin polarization so that a virtually half-metallic interface can be achieved, for comparably moderate strain. © 2012 The Royal Society of Chemistry.

  8. AN EXTREMELY CARBON-RICH, EXTREMELY METAL-POOR STAR IN THE SEGUE 1 SYSTEM

    International Nuclear Information System (INIS)

    Norris, John E.; Yong, David; Gilmore, Gerard; Wyse, Rosemary F. G.; Frebel, Anna

    2010-01-01

    We report the analysis of high-resolution, high signal-to-noise ratio, spectra of an extremely metal-poor, extremely C-rich red giant, Seg 1-7, in Segue 1-described in the literature alternatively as an unusually extended globular cluster or an ultra-faint dwarf galaxy. The radial velocity of Seg 1-7 coincides precisely with the systemic velocity of Segue 1, and its chemical abundance signature of [Fe/H] = -3.52, [C/Fe] = +2.3, [N/Fe] = +0.8, [Na/Fe] = +0.53, [Mg/Fe] = +0.94, [Al/Fe] = +0.23, and [Ba/Fe] < -1.0 is similar to that of the rare and enigmatic class of Galactic halo objects designated CEMP-no (carbon-rich, extremely metal-poor with no enhancement (over solar ratios) of heavy neutron-capture elements). This is the first star in a Milky Way 'satellite' that unambiguously lies on the metal-poor, C-rich branch of the Aoki et al. bimodal distribution of field halo stars in the ([C/Fe], [Fe/H])-plane. Available data permit us only to identify Seg 1-7 as a member of an ultra-faint dwarf galaxy or as debris from the Sgr dwarf spheroidal galaxy. In either case, this demonstrates that at extremely low abundance, [Fe/H ] <-3.0, star formation and associated chemical evolution proceeded similarly in the progenitors of both the field halo and satellite systems. By extension, this is consistent with other recent suggestions that the most metal-poor dwarf spheroidal and ultra-faint dwarf satellites were the building blocks of the Galaxy's outer halo.

  9. Large resistivity modulation in mixed-phase metallic systems.

    Science.gov (United States)

    Lee, Yeonbae; Liu, Z Q; Heron, J T; Clarkson, J D; Hong, J; Ko, C; Biegalski, M D; Aschauer, U; Hsu, S L; Nowakowski, M E; Wu, J; Christen, H M; Salahuddin, S; Bokor, J B; Spaldin, N A; Schlom, D G; Ramesh, R

    2015-01-07

    In numerous systems, giant physical responses have been discovered when two phases coexist; for example, near a phase transition. An intermetallic FeRh system undergoes a first-order antiferromagnetic to ferromagnetic transition above room temperature and shows two-phase coexistence near the transition. Here we have investigated the effect of an electric field to FeRh/PMN-PT heterostructures and report 8% change in the electrical resistivity of FeRh films. Such a 'giant' electroresistance (GER) response is striking in metallic systems, in which external electric fields are screened, and thus only weakly influence the carrier concentrations and mobilities. We show that our FeRh films comprise coexisting ferromagnetic and antiferromagnetic phases with different resistivities and the origin of the GER effect is the strain-mediated change in their relative proportions. The observed behaviour is reminiscent of colossal magnetoresistance in perovskite manganites and illustrates the role of mixed-phase coexistence in achieving large changes in physical properties with low-energy external perturbation.

  10. Direct selenylation of mixed Ni/Fe metal-organic frameworks to NiFe-Se/C nanorods for overall water splitting

    Science.gov (United States)

    Xu, Bo; Yang, He; Yuan, Lincheng; Sun, Yiqiang; Chen, Zhiming; Li, Cuncheng

    2017-10-01

    Development of low-cost, highly active bifunctional catalyst for efficient overall water splitting based on earth-abundant metals is still a great challenging task. In this work, we report a NiFe-Se/C composite nanorod as efficient non-precious-metal electrochemical catalyst derived from direct selenylation of a mixed Ni/Fe metal-organic framework. The as-obtained catalyst requires low overpotential to drive 10 mA cm-2 for HER (160 mV) and OER (240 mV) in 1.0 M KOH, respectively, and its catalytic activity is maintained for at least 20 h. Moreover, water electrolysis using this catalyst achieves high water splitting current density of 10 mA cm-2 at cell voltage of 1.68 V.

  11. Thermodynamic modeling of the Fe-Mg-Si system

    Directory of Open Access Journals (Sweden)

    Du Y.

    2007-01-01

    Full Text Available A thermo dynamic modeling for the Fe-Mg-Si system is conducted. All of the experimental phase diagram and thermodynamic data available from the literature are critically reviewed and assessed using thermo dynamic models for the Gibbs energies of individual phases. The thermodynamic parameters for ternary liquid as well as binary phases αFeSi, (high-temperature form of FeSi2 and FeSi showing noticeable solubilities for Mg are evaluated in the optimization. Comparisons between the calculated and measured phase diagrams show that the measured isothermal six-lions at 1600°, 1454°, 727° and 710°C, the observed regions of primary phases are satisfactorily accounted for by the thermodynamic description. The limited thermodynamic data concerning the activity of Mg in liquid at 1350°C are found to be inconsistent with the well established phase relations. The liquidus projection and reaction scheme for the entire Fe-Mg-Si system are also presented. .

  12. Effect of metal ion Fe(III on the performance of chlorophyll as photosensitizers on dye sensitized solar cell

    Directory of Open Access Journals (Sweden)

    Harsasi Setyawati

    Full Text Available The energy crisis is a major problem facing the world today and will need a renewable energy source that is environmentally friendly; one of these is the dye sensitized solar cell (DSSC. DSSC is photochemical electric cell that can convert solar energy into electrical energy. This research aims to study the characteristics of chlorophyll compounds with the addition of metal ions Fe(III and to determine the effect of Fe(III on the performance of chlorophyll as a photosensitizer in the DSSC. The formation of complex compounds of Fe(III-chlorophyll is shown by the phenomenon of metal ligand charge transfer (MLCT at a wavelength of 263.00 nm and absorption transition d-d at 745.00 nm. Fourier transform infrared characterization of the binding of Fe-O complex compounds appears at 486.06 cm−1. The complex compound of Fe(III-chlorophyll has a magnetic moment value of 9.62 Bohr Magneton (BM. The existence of ion Fe(III in chlorophyll can improve the performance of chlorophyll as a dye sensitizer with a maximum current of 4.00 mA/cm2, maximum voltage of 0.18 volts and efficiency values of 1.35%. Keywords: Fe(III-chlorophyll, Dye sensitized solar cell, Metal ligand charge transfer, Photosensitizer

  13. Theoretical bases on thermal stability of layered metallic systems

    International Nuclear Information System (INIS)

    Kadyrzhanov, K.K.; Rusakov, V.S.; Turkebaev, T.Eh.; Zhankadamova, A.M.; Ensebaeva, M.Z.

    2003-01-01

    The paper is dedicated to implementation of the theoretical bases for layered metallic systems thermal stabilization. The theory is based on the stabilization mechanism expense of the intermediate two-phase field formation. As parameters of calculated model are coefficients of mutual diffusion and inclusions sizes of generated phases in two-phase fields. The stabilization time dependence for beryllium-iron (Be (1.1 μm)-Fe(5.5 μm)) layered system from iron and beryllium diffusion coefficients, and inclusions sizes is shown as an example. Conclusion about possible mechanisms change at transition from microscopic consideration to the nano-crystal physics level is given

  14. Competition of dipositive metal ions for Fe (III) binding sites in chelation therapy of Iron Load

    International Nuclear Information System (INIS)

    Rehmani, Fouzia S.

    2005-01-01

    Iron overload is a condition in which excessive iron deposited in the liver, kidney and spleen of human beings in the patients of beta thalassemia and sickle cell anemia. Instead of its importance iron could be toxic when in excess, it damages the tissues. For the treatment of iron overload, a drug desferrioxamine mesylate has been used. It is linear trihydroxamic acid, a natural siderophore produced by streptomyces which removes the extra iron from body. Salicylhydroxamate type siderphore. In present research salicylhydroxamate was used for the complexation with dipositive metal ions which are available in biological environments such as Mn (II), Co (II), Ni (II) and Cu (II). The aim of our work was to study the competition reactions between Fe (III) and other dipositive ions; to calculate the thermodynamic data of chelation of these metal ions complexes with hydroxamate by computer program and comparison with hydroxamate complexes. (author)

  15. Contrasting Effects of Carbon and Sulfur on Fe-Isotope Fractionation between Metal and Silicate Melt during Planetary Core Formation

    Science.gov (United States)

    Elardo, S. M.; Shahar, A.

    2015-12-01

    There are numerous studies that show well-resolved Fe isotope fractionations in igneous materials from different planetary bodies. Potential explanations for these fractionations include a non-chondritic bulk planetary Fe isotopic composition, and equilibrium fractionation between Fe-alloys or minerals and silicate melts during planetary differentiation, mantle melting, or fractional crystallization. This is further complicated by the fact that these processes are not mutually exclusive, making the interpretation of Fe isotope data a complex task. Here we present new experimental results investigating the effect of C on Fe isotope fractionation between molten peridotite and an Fe-alloy. Experiments were conducted at 1 GPa and 1850° C for 0.5 - 3 hours on a mixture of an 54Fe-spiked peridotite and Fe-metal with and without Ni metal in an end-loaded piston cylinder at the Geophysical Laboratory. Carbon saturation was achieved with a graphite capsule, and resulted in C contents of the Fe-alloy in our experiments ranging from 3.8 - 4.9 wt. %. The metal and silicate phases from half of each experiment were separated manually and dissolved in concentrated acids. Iron was separated from matrix elements by anion exchange chromatagraphy. Iron-isotopic compositions were determined with the Nu Plasma II MC-ICP-MS at GL. The other half of each experiment was used for quantitative microbeam analysis. Equilibrium was assessed with a time series and the three-isotope exchange method. The Ni-free experiments resulted in no resolvable Fe isotope fractionation between the Fe-C-alloy and molten silicate. This is in contrast to the results of Shahar et al. (2015) which showed a fractionation for Δ57Fe of ~0.18 ‰ between a peridotite and an Fe-alloy with a similar S abundance to C in these experiments. The one experiment thus far that contained Ni (~4 wt. % in the alloy) showed a resolvable fractionation between the Fe-Ni-C alloy and silicate of ~0.10 ‰. Shahar et al. found a

  16. Exploiting differential electrochemical stripping behaviors of Fe3O4 nanocrystals toward heavy metal ions by crystal cutting.

    Science.gov (United States)

    Yao, Xian-Zhi; Guo, Zheng; Yuan, Qing-Hong; Liu, Zhong-Gang; Liu, Jin-Huai; Huang, Xing-Jiu

    2014-08-13

    This study attempts to understand the intrinsic impact of different morphologies of nanocrystals on their electrochemical stripping behaviors toward heavy metal ions. Two differently shaped Fe3O4 nanocrystals, i.e., (100)-bound cubic and (111)-bound octahedral, have been synthesized for the experiments. Electrochemical results indicate that Fe3O4 nanocrystals with different shapes show different stripping behaviors toward heavy metal ions. Octahedral Fe3O4 nanocrystals show better electrochemical sensing performances toward the investigated heavy metal ions such as Zn(II), Cd(II), Pb(II), Cu(II), and Hg(II), in comparison with cubic ones. Specifically, Pb(II) is found to have the best stripping performance on both the (100) and (111) facets. To clarify these phenomena, adsorption abilities of as-prepared Fe3O4 nanocrystals have been investigated toward heavy metal ions. Most importantly, combined with theoretical calculations, their different electrochemical stripping behaviors in view of facet effects have been further studied and enclosed at the level of molecular/atom. Finally, as a trial to find a disposable platform completely free from noble metals, the potential application of the Fe3O4 nanocrystals for electrochemical detection of As(III) in drinking water is demonstrated.

  17. Phase analysis of Fe-B-V system

    Czech Academy of Sciences Publication Activity Database

    Homolová, V.; Výrostková, A.; Čiripová, L.; Kroupa, Aleš

    2013-01-01

    Roč. 51, č. 2 (2013), s. 135-139 ISSN 0023-432X R&D Projects: GA ČR(CZ) GAP108/10/1908 Institutional support: RVO:68081723 Keywords : CALPHAD method * Fe-B-V system * phase diagram Subject RIV: BJ - Thermodynamics Impact factor: 0.546, year: 2013

  18. Thermodynamic modeling of the Co-Fe-O system

    DEFF Research Database (Denmark)

    Zhang, Weiwei; Chen, Ming

    2013-01-01

    As a part of the research project aimed at developing a thermodynamic database of the La-Sr-Co-Fe-O system for applications in Solid Oxide Fuel Cells (SOFCs), the Co-Fe-O subsystem was thermodynamically re-modeled in the present work using the CALPHAD methodology. The solid phases were described...... using the Compound Energy Formalism (CEF) and the ionized liquid was modeled with the ionic two-sublattice model based on CEF. A set of self-consistent thermodynamic parameters was obtained eventually. Calculated phase diagrams and thermodynamic properties are presented and compared with experimental...

  19. Magnetic properties of (misch metal, Nd-Fe-B melt-spun magnets

    Directory of Open Access Journals (Sweden)

    R. Li

    2017-05-01

    Full Text Available The effect of replacing Nd with misch metal (MM on magnetic properties and thermal stability has been investigated on melt-spun (Nd1-xMMx13.5Fe79.5B7 ribbons by varying x from 0 to 1. All of the alloys studied crystallize in the tetragonal 2:14:1 structure with single hard magnetic phase. Curie temperature (Tc, coercivity (Hcj, remanence magnetization (Br and maximum energy product ((BHmax all decrease with MM content. The melt-spun MM13.5Fe79.5B ribbons with high ratio of La and Ce exhibit high magnetic properties of Hcj = 8.2 kOe and (BHmax= 10.3 MGOe at room temperature. MM substitution also significantly strengthens the temperature stability of coercivity. The coercivities of the samples with x = 0.2 and even 0.4 exhibit large values close to that of Nd13.5Fe79.5B7 ribbons above 400 K.

  20. FeS-Quantum-Dot Sensitized Metal Oxide Photoelectrodes: Photoelectrochemistry and Photoinduced Absorption Spectroscopy

    Directory of Open Access Journals (Sweden)

    Idriss Bedja

    2011-01-01

    Full Text Available TiO2, ZnO nanoparticulate(-np, and ZnO-nanorod(-nr electrodes have been modified with FeS2 (pyrite nanoparticles. Quantum size effect is manifested by a blue shift in both absorption and photocurrent action spectra. PIA (photoinduced absorption spectroscopy, a multipurpose tool in the study of dye-sensitized solar cells, is used to study quantum-dot modified metal oxide (MO nanostructured electrodes. The PIA spectra showed an evidence for long-lived photoinduced charge separation. Time-resolved PIA showed that recombination between electrons and holes occurs on a millisecond timescale. Incident-photon-to-current efficiencies at 400 nm are ranged between 13% and 25%. The better solar cell performance of FeS2 on ZnO-nr over ZnO-np can be ascribed to the faster, unidirectional e-transport channels through the ZnO-nr as well as the longer electron lifetimes. The lower performances of electrodes can be explained by the presence of FeS2 phases other than the photoactive pyrite phase, as evidenced from XRD study.

  1. Formation of centimeter Fe-based bulk metallic glasses in low vacuum environment

    Energy Technology Data Exchange (ETDEWEB)

    Pan Jie; Chen Qi; Li Ning [State Key Lab of Materials Processing and Mould Technology, Department of Materials Science and Technology, Huazhong University of Science and Technology, 430074 Wuhan (China); Liu Lin [State Key Lab of Materials Processing and Mould Technology, Department of Materials Science and Technology, Huazhong University of Science and Technology, 430074 Wuhan (China)], E-mail: lliu2000@public.wh.hb.cn

    2008-09-08

    The formation of a Fe{sub 43.7}Co{sub 7.3}Cr{sub 14.7}Mo{sub 12.6}C{sub 15.5}B{sub 4.3}Y{sub 1.9} bulk metallic glass (BMG) was attempted in low vacuum environment and in air using commercial raw materials. The glass forming ability of the Fe-based alloys was studied by X-ray diffraction (XRD), differential scanning calorimetry (DSC) and differential thermal analyzer (DTA). It was found that cylindric rods with diameters ranging from 10 mm to 5 mm could be successfully fabricated by copper-mold casting in the pressures from 1.5 Pa to 10{sup 5} Pa (10{sup 5} Pa = 1 atm). All BMGs exhibit a distinct glass transition and wide supercooled liquid region. The preparation condition seems not significantly affected by the thermodynamic parameters of BMG, such as supercooled liquid region, glass transition temperature and melting process. The oxygen content of the alloys prepared in different vacuum conditions was measured by a LECO oxygen analyzer, which revealed that the oxygen content was less than 100 ppm for all BMGs prepared, even in air. The good glass forming ability and excellent oxidation resistance for the present Fe-based alloy are discussed.

  2. Corrosion study of Fe-based bulk metallic glasses in chloride medium

    International Nuclear Information System (INIS)

    Waqas, M.U.

    2010-01-01

    Bulk metallic glasses (amorphous metals) are an emerging class of alloys due to their unique set of properties. They exhibit excellent mechanical strength, high hardness and corrosion resistance. Unlike other new materials, which are developed to fulfill a particular need, BMGs came to existence without any application, so the uses of BMGs are yet to be exploited. Before putting BMGs into applications, their properties must be fully understood, particularly the corrosion resistance against a working environment. Fe-based amorphous alloys are particularly important for their future use as structural materials due to their high strength and cheap raw materials. Some Fe-based amorphous alloys exhibit excellent soft magnetic properties, which make them feasible to be used as transformer materials. Some compositions are also competitive to replace the existing bio-materials like 316L SS due to their better biocompatibility. Fe-based amorphous alloys can also be used as thermal-spray coatings due to their unchanged corrosion resistance as compared to bulk alloy. Many electrochemical studies have been done to investigate the corrosion resistance of Fe- based BMG that showed its excellent corrosion resistance. Still not enough data is available and further work is needed to be done in this field. In the present study, corrosion of Fe/sub 50/Cr/sub 14/Mo/sub 14/C/sub 14/B/sub 6/X/sub 2/ (X = Y, Gd, and Dy), designated as S1, S2 and S3 respectively, was investigated in 4M NaCI solution. The corrosion study was done using potentiodynamic polarization test and accelerated corrosion test at a current density of 6mA.cm/sup -2/. Following this; corrosion morphology was investigated by scanning electron microscope, while compositional analysis was done by energy dispersive x-ray spectroscope (EDX) attached with SEM. S1 and S3 showed similar corrosion behavior with S3 having the highest corrosion resistance while S2 have different corrosion behavior as well as least corrosion

  3. Redox Dynamics of Mixed Metal (Mn, Cr, and Fe) Ultrafine Particles

    Energy Technology Data Exchange (ETDEWEB)

    Nico, Peter S.; Kumfer, Benjamin M.; Kennedy, Ian M.; Anastasio, Cort

    2008-08-01

    The impact of particle composition on metal oxidation state, and on changes in oxidation state with simulated atmospheric aging, are investigated experimentally in flame-generated nanoparticles containing Mn, Cr, and Fe. The results demonstrate that the initial fraction of Cr(VI) within the particles decreases with increasing total metal concentration in the flame. In contrast, the initial Mn oxidation state was only partly controlled by metal loading, suggesting the importance of other factors. Two reaction pathways, one reductive and one oxidative, were found to be operating simultaneously during simulated atmospheric aging. The oxidative pathway depended upon the presence of simulated sunlight and O{sub 3}, whereas the reductive pathway occurred in the presence of simulated sunlight alone. The reductive pathway appears to be rapid but transient, allowing the oxidative pathway to dominate with longer aging times, i.e. greater than {approx}8 hours. The presence of Mn within the particles enhanced the importance of the oxidative pathway, leading to more net Cr oxidation during aging implying that Mn can mediate oxidation by removal of electrons from other particulate metals.

  4. The supercooled liquid region span of Fe-based bulk metallic glasses

    Energy Technology Data Exchange (ETDEWEB)

    Ferenc, Jaroslaw, E-mail: jferenc@inmat.pw.edu.p [Faculty of Materials Science and Engineering, Warsaw University of Technology, ul. Woloska 141, 02-507 Warsaw (Poland); Erenc-Sedziak, Tatiana; Kowalczyk, Maciej; Kulik, Tadeusz [Faculty of Materials Science and Engineering, Warsaw University of Technology, ul. Woloska 141, 02-507 Warsaw (Poland)

    2010-04-16

    This work presents the results of the study of the magnetically soft, iron-based bulk metallic glasses, from the viewpoint of their ability to deform in the supercooled liquid region and to resist the tendency to crystallise. The calorimetric measurements of glass transition and crystallisation temperatures (T{sub g} and T{sub x1} respectively) were employed, accompanied by the measurements of magnetic properties as the monitor of structural changes after heat treatment. It was found that the widest supercooled liquid region was obtained when zirconium was selected as one of the alloying elements, yielding the T{sub x1}-T{sub g} span of about 70 {sup o}C. Also, it was observed that the values of T{sub g} and T{sub x} may be controlled by the proportions of the main elements (Fe, Co, Ni), and the glass forming elements (such as B, Nb, Zr). As a guideline, it is suggested that the glassy Fe-based alloys may be maintained in the supercooled liquid state without crystallisation for several minutes, if T{sub x1}-T{sub g} is wider than 50 {sup o}C. Basing on this estimation, calorimetric measurements may be a good indicator of the ability of bulk metallic glasses to be suitable for superplastic compaction into larger shapes.

  5. Heavy metal (Pd, Cd, Fe, Zn and Mn) levels in sediments from Nigerian Coastal waters.

    Science.gov (United States)

    Oguguah, N. M.

    2016-02-01

    Sediments collected during a pollution monitoring cruise carried out on Nigerian coastal waters by Nigerian Institute for Oceanography and Marine Research Lagos was analysed for heavy metals. A trawler MS Suzzannah with an on board GPS was used to locate bearings of 25 sampling points (N06o30 and E003o30). Eckman grab was deployed and used in collecting bottom sediments. The sediment were air dried and digested using the method of GEF GCLME. The samples were analysed in five replicates for heavy metals (Pd, Cd, Fe, Zn and Mn) using Varian AA 600 Atomic Absorption Spectrometer. The highest concentration of Pb was transect R (10.93) and the least concentration (0.059) was in transect C. The highest concentration of Cd was transect H (0.75) and the least concentration (0.044) was in transect C. The highest concentration of Fe was transect M (203.582) and the least concentration (2.232) was in transect C. The highest concentration of Zn was transect H (4.595) and the least concentration (0.174) was in transect F. The highest concentration of Mn was transect H (209.251) and the least concentration (0.167) was in transect C.

  6. Metallization of some simple systems

    International Nuclear Information System (INIS)

    Ross, M.; McMahan, A.K.

    1981-01-01

    We discuss the metallization of Xe, Ar, He, I 2 , H 2 , and N 2 in terms of some recent theoretical work and shock-wave experiments. New shock-wave data on liquid hydrogen and deuterium leads to a predicted pressure above 3 Mbar for the appearance of a monatomic metal phase. We expect CsI to become metallic near 0.8 Mbar

  7. The ferromagnetic shape memory system Fe-Pd-Cu

    Energy Technology Data Exchange (ETDEWEB)

    Hamann, S. [Institute of Materials, Faculty of Mechanical Engineering, Ruhr-University Bochum, 44801 Bochum (Germany); Gruner, M.E. [Faculty of Physics and Center for Nanointegration, CeNIDE, University of Duisburg-Essen, 47048 Duisburg (Germany); Irsen, S. [Forschungszentrum caesar, Electron Microscopy, 53175 Bonn (Germany); Buschbeck, J. [IFW Dresden, P.O. Box: 270116, 01171 Dresden (Germany); Bechtold, C. [Inorganic Functional Materials, Christian-Albrechts-University, 24143 Kiel (Germany); Kock, I. [I. Physikalisches Institut, Georg-August-University Goettingen, 37077 Goettingen (Germany); Mayr, S.G. [I. Physikalisches Institut, Georg-August-University Goettingen, 37077 Goettingen (Germany)] [Leibniz-Institut fuer Oberflaechenmodifizierung eV, Translationszentrum fuer regenerative Medizin und Fakultaet fuer Physik und Geowissenschaften, University Leipzig, 04318 Leipzig (Germany); Savan, A.; Thienhaus, S. [Institute of Materials, Faculty of Mechanical Engineering, Ruhr-University Bochum, 44801 Bochum (Germany); Quandt, E. [Inorganic Functional Materials, Christian-Albrechts-University, 24143 Kiel (Germany); Faehler, S. [IFW Dresden, P.O. Box: 270116, 01171 Dresden (Germany); Entel, P. [Faculty of Physics and Center for Nanointegration, CeNIDE, University of Duisburg-Essen, 47048 Duisburg (Germany); Ludwig, A., E-mail: alfred.ludwig@rub.de [Institute of Materials, Faculty of Mechanical Engineering, Ruhr-University Bochum, 44801 Bochum (Germany)

    2010-10-15

    A new ferromagnetic shape memory thin film system, Fe-Pd-Cu, was developed using ab initio calculations, combinatorial fabrication and high-throughput experimentation methods. Reversible martensitic transformations are found in extended compositional regions, which have increased fcc-fct transformation temperatures in comparison to previously published results. High resolution transmission electron microscopy verified the existence of a homogeneous ternary phase without precipitates. Curie temperature, saturation polarization and orbital magnetism are only moderately decreased by alloying with nonmagnetic Cu. Compared to the binary system; enhanced Invar-type thermal expansion anomalies in terms of an increased volume magnetostriction are predicted. Complementary experiments on splat-fabricated bulk Fe-Pd-Cu samples showed an enhanced stability of the disordered transforming Fe{sub 70}Pd{sub 30} phase against decomposition. From the comparison of bulk and thin film results, it can be inferred that, for ternary systems, the Fe content, rather than the valence electron concentration, should be regarded as the decisive factor determining the fcc-fct transformation temperature.

  8. Technique for recovering rare-earth metals from spent sintered Nd-Fe-B magnets without external heating

    Directory of Open Access Journals (Sweden)

    Ryo Sasai

    2016-06-01

    Full Text Available To selectively recover rare-earth metals with higher purity from spent sintered Nd-Fe-B magnets without external heating, we investigated the mechano-chemical treatment of spent sintered Nd-Fe-B magnet powder with a reaction solution of HCl and (COOH2 at room temperature. The results of various experiments showed that the mechano-chemical treatment with HCl and (COOH2 is very effective for recovering the rare-earth metals contained in spent sintered Nd-Fe-B magnet powder; the recovery rate and purity of the rare-earth metals were 95.3 and 95.0 mass%, respectively, under optimal conditions ([HCl] = 0.2 mol/dm3 and [(COOH2] = 0.25 mol/dm3.

  9. Metal-carbon nanosystem IR-PVA/Fe-Co for catalysis in the Fischer-Tropsch synthesis

    International Nuclear Information System (INIS)

    Vasilev, A A; Dzidziguri, E L; Ivantsov, M I; Efimov, M N

    2016-01-01

    Metal-carbon nanosystems consisting of nanodimensional bimetallic particles of Fe- Co dispersed in a carbon matrix for the Fischer-Tropsch synthesis were studied. Prepared metal-carbon nanopowders samples were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and scanning electron microscopy (SEM). It was shown formation of FeCo nanoparticles with body-centered cubic structures started at 400 °C. FeCo nanoparticles have spherical form, the mean size is 7 - 12 nm and uniform distribution in a carbon matrix. The metal-carbon nanosystem demonstrates a catalytic activity in the Fischer- Tropsch synthesis. The maximum yield of liquid hydrocabons C 5+ was 92 g/m 3 while the selectivity for the target product - 35%. (paper)

  10. The interface of the ferromagnetic metal CoS2 and the nonmagnetic semiconductor FeS2

    KAUST Repository

    Nazir, S.

    2010-11-05

    The electronic and magnetic properties of the cubic pyriteCoS2/FeS2interface are studied using the all-electron full-potential linearized augmented plane wave method. We find that this contact between a ferromagneticmetal and a nonmagnetic semiconductor shows a metallic character. The CoS2 stays close to half-metallicity at the interface, while the FeS2 becomes metallic. The magnetic moment of the Co atoms at the interface slightly decreases as compared to the bulk value and a small moment is induced on the Fe atoms. Furthermore, at the interfaceferromagnetic ordering is found to be energetically favorable as compared to antiferromagnetic ordering.

  11. Regulation of brain copper homeostasis by the brain barrier systems: Effects of Fe-overload and Fe-deficiency

    International Nuclear Information System (INIS)

    Monnot, Andrew D.; Behl, Mamta; Ho, Sanna; Zheng, Wei

    2011-01-01

    Maintaining brain Cu homeostasis is vital for normal brain function. The role of systemic Fe deficiency (FeD) or overload (FeO) due to metabolic diseases or environmental insults in Cu homeostasis in the cerebrospinal fluid (CSF) and brain tissues remains unknown. This study was designed to investigate how blood-brain barrier (BBB) and blood-SCF barrier (BCB) regulated Cu transport and how FeO or FeD altered brain Cu homeostasis. Rats received an Fe-enriched or Fe-depleted diet for 4 weeks. FeD and FeO treatment resulted in a significant increase (+ 55%) and decrease (− 56%) in CSF Cu levels (p < 0.05), respectively; however, neither treatment had any effect on CSF Fe levels. The FeD, but not FeO, led to significant increases in Cu levels in brain parenchyma and the choroid plexus. In situ brain perfusion studies demonstrated that the rate of Cu transport into the brain parenchyma was significantly faster in FeD rats (+ 92%) and significantly slower (− 53%) in FeO rats than in controls. In vitro two chamber Transwell transepithelial transport studies using primary choroidal epithelial cells revealed a predominant efflux of Cu from the CSF to blood compartment by the BCB. Further ventriculo-cisternal perfusion studies showed that Cu clearance by the choroid plexus in FeD animals was significantly greater than control (p < 0.05). Taken together, our results demonstrate that both the BBB and BCB contribute to maintain a stable Cu homeostasis in the brain and CSF. Cu appears to enter the brain primarily via the BBB and is subsequently removed from the CSF by the BCB. FeD has a more profound effect on brain Cu levels than FeO. FeD increases Cu transport at the brain barriers and prompts Cu overload in the CNS. The BCB plays a key role in removing the excess Cu from the CSF.

  12. Mechanical alloying in the Fe-Cu system

    DEFF Research Database (Denmark)

    Jiang, Jianzhong; Gente, C.; Bormann, R.

    1998-01-01

    The studies of mechanical alloying on the Fe-Cu system, as a model system for those with positive heats of mixing, are reviewed. Several problems involved in the mechanical alloying process are discussed. For example, (1) whether alloying occurs on an atomic level; (2) what the solid solubility...... in the Fe-Cu system is; (3) where the positive energy is stored in the alloys; (4) what the decomposition process of the supersaturated alloys is; and (5) what type of magnetic properties the new materials have. The elucidation of these problems will shed light on the understanding of the mechanisms...... for the preparation of materials under highly non-equilibrium conditions in systems with positive heats of mixing by mechanical alloying....

  13. Formation of Fe-Nb-X (X=Zr, Ti) amorphous alloys from pure metal elements by mechanical alloying

    Energy Technology Data Exchange (ETDEWEB)

    Xiao Zhiyu [National Engineering Research Center of Near-net-shape Forming for Metallic Materials, South China University of Technology, Guangzhou 510640 (China); Tang Cuiyong, E-mail: hnrtcy@163.com [National Engineering Research Center of Near-net-shape Forming for Metallic Materials, South China University of Technology, Guangzhou 510640 (China); Ngai, Tungwai Leo; Yang Chao; Li Yuanyuan [National Engineering Research Center of Near-net-shape Forming for Metallic Materials, South China University of Technology, Guangzhou 510640 (China)

    2012-01-15

    Fe-based amorphous powders of Fe{sub 56}Nb{sub 6}Zr{sub 38} and Fe{sub 60}Nb{sub 6}Ti{sub 34} based on binary eutectic were prepared by mechanical alloying starting from mixtures of pure metal powders. The amorphization behavior and thermal stability were examined by x-ray diffraction, scanning electron microscopy, transmission electron microscopy and differential scanning calorimetry. Results show that Fe{sub 56}Nb{sub 6}Zr{sub 38} alloy has a better glass forming ability and a relatively lower thermal stability comparing with Fe{sub 60}Nb{sub 6}Ti{sub 34} alloy. The prepared amorphous powders have homogeneous element distribution and no obvious contaminants coming from mechanical alloying. The synthesized amorphous powders offer the potential for consolidation to full density with desirable mechanical properties through the powder metallurgy methods.

  14. Effect of hydrogen on the melting of the Fe-C system and the fate of the subducted carbon

    Science.gov (United States)

    Lai, X.; Chen, B.; Gao, J.; Zhu, F.

    2017-12-01

    The subducted oceanic crust carries significant amount of carbonates and organic carbons from the surface into the deep mantle. Through slab-mantle interactions, subducted carbons can react with metallic iron in the metal-saturated regions of the mantle and form various reduced species such as Fe carbides. The Fe-C system is found to have higher eutectic melting temperature than mantle geotherm and thus carbon by forming iron carbides may be "redox freezed" in the mantle (Rohrbach and Schmidt 2011). Hydrogen was found to be have significant effect on the melting of the Fe-light-elements systems such as the Fe-S system (Shibazaki et al., 2011). Here we report experimental results from both multi-anvil press and diamond anvil cell experiments on the melting behaviors of the Fe-C-H system. C14H12, a solid-state C-H organic compound was used as a C-H source to react with the metallic iron at high pressure and high temperature conditions. With excess C14H12, hydrogen in the FeHx alloy was totally replaced by carbon at 14.8-24.7 GPa. Conversely, with excess Fe, the existence of hydrogen is found to depress the melting temperature of the Fe-C system by at least 100 K. Hydrogen may facilitate the transport and cycling of subducted carbon in the deep mantle and contribute to formation of superdeep diamonds (Smith et al. 2016). Rohrbach, Arno, and Max W. Schmidt. "Redox freezing and melting in the Earth's deep mantle resulting from carbon-iron redox coupling." Nature 472.7342 (2011): 209. Shibazaki, Yuki, et al. "Effect of hydrogen on the melting temperature of FeS at high pressure: Implications for the core of Ganymede." Earth and Planetary Science Letters 301.1 (2011): 153-158. Smith, Evan M., et al. "Large gem diamonds from metallic liquid in Earth's deep mantle." Science 354.6318 (2016): 1403-1405.

  15. Ferromagnetism and suppression of metallic clusters in Fe implanted ZnO -- a phenomenon related to defects?

    Energy Technology Data Exchange (ETDEWEB)

    Arenholz, Elke; Zhou, S.; Potzger, K.; Talut, G.; Reuther, H.; Kuepper, K.; Grenzer, J.; Xu, Q.; Mucklich, A.; Helm, M.; Fassbender, J.; Arenholz, E.

    2008-03-12

    We investigated ZnO(0001) single crystals annealed in high vacuum with respect to their magnetic properties and cluster formation tendency after implant-doping with Fe. While metallic Fe cluster formation is suppressed, no evidence for the relevance of the Fe magnetic moment to the observed ferromagnetism was found. The latter along with the cluster suppression is discussed with respect to defects in the ZnO host matrix, since the crystalline quality of the substrates was lowered due to the preparation as observed by x-ray diffraction.

  16. Contamination assessment of heavy metals in the soils around Khouzestan Steel Company (KSC (Ni, Mn, Pb, Fe, Zn, Cr

    Directory of Open Access Journals (Sweden)

    Fatemeh hormozi Nejad

    2017-02-01

    Full Text Available Introduction Soil plays a vital role in human life as the very survival of mankind is tied to the preservation of soil productivity (Kabata- Pendies and Mukherjee, 2007. The purpose of this study is the assessment of heavy metal contamination (Zn, Mn, Pb, Fe, Ni, Cr of the soil around the Khuzestan Steel Complex. Materials and methods For this purpose, 13 surface soil samples (0-10 cm were taken. Also a control sample was taken from an area away from the steel complex. The coordinates of each point were recorded by Global Positioning System (GPS. The samples were transferred to the laboratory and then were air dried at room temperature for 72 hours. Then they were sieved through a 2mm sieve for determining physical and chemical parameters (soil texture, pH, OC, and a 63-micron sieve for measurement of heavy metal concentration. pH was measured using a calibrated pH meter at a 2: 1 mixture (soil: water, and soil texture was determined using a hydrometer. The amount of organic matter was measured using the Valkey black method (Chopin and Alloway, 2007. After preparation of the samples in the laboratory, the samples were analyzed using the ICP-OES method to assess concentration of heavy metals. Measurement of heavy metals concentration was carried out at the Zar azma laboratory in Tehran. To ensure the accuracy of the analysis of soil samples, replicate samples were also sent to the laboratory. In order to assess the heavy metal pollution in the soil samples, different indices including contamination factor (CF, contamination degree (Cd, anthropogenic enrichment percent (An%, and saturation degree of metals (SDM were calculated. Discussion In addition, the mean concentrations of heavy metals in soil samples were compared to the concentration of these metals in Control Sample and unpolluted soil standard. Measurement of soil pH showed that the soil has a tendency to alkalinity. Also, soil texture is sandy loam (Moyes, 2011. The results showed that

  17. in biomass-fired boilers for Fe-O-Cl-S system

    Directory of Open Access Journals (Sweden)

    Kaczmarczyk Robert

    2017-01-01

    Full Text Available The paper presents a thermodynamic analysis of chlorideinduced corrosion in the Fe-O-Cl-S system. The influence of steam concentration in the gas phase on chloride-induced corrosion process was presented. Based on the parametric equations the equilibrium concentration of the gas phase was determined. The effect of alkali metals chlorides in gas phase (Na,KCl on formation of (Na,KFeO2 in the passive oxide scale layer (FeO/Fe3O4/Fe2O3 was analysed. Condensation of (Na,KCl vapors, formation of low-melting eutectic mixtures in deposits and consequences of this process on corrosion process were examined. Additionally, the role of SO2 in chlorination and oxidation process of steel in melted ash deposits was discussed as well. The results were correlated with available in the literature laboratory experimental data and industrial corrosion process observations. Presented thermodynamic analysis was compared with assumptions of an “active oxidation” model. The results may be used for experimental research planning and a corrosion process prevention in the industry.

  18. Shewanella oneidensis: a new and efficient System for Expression and Maturation of heterologous [Fe-Fe] Hydrogenase from Chlamydomonas reinhardtii

    Directory of Open Access Journals (Sweden)

    Sybirna Kateryna

    2008-09-01

    Full Text Available Abstract Background The eukaryotic green alga, Chlamydomonas reinhardtii, produces H2 under anaerobic conditions, in a reaction catalysed by a [Fe-Fe] hydrogenase HydA1. For further biochemical and biophysical studies a suitable expression system of this enzyme should be found to overcome its weak expression in the host organism. Two heterologous expression systems used up to now have several advantages. However they are not free from some drawbacks. In this work we use bacterium Shewanella oneidensis as a new and efficient system for expression and maturation of HydA1 from Chlamydomonas reinhardtii. Results Based on codon usage bias and hydrogenase maturation ability, the bacterium S. oneidensis, which possesses putative [Fe-Fe] and [Ni-Fe] hydrogenase operons, was selected as the best potential host for C. reinhardtii [Fe-Fe] hydrogenase expression. Hydrogen formation by S. oneidensis strain AS52 (ΔhydAΔhyaB transformed with a plasmid bearing CrHydA1 and grown in the presence of six different substrates for anaerobic respiration was determined. A significant increase in hydrogen evolution was observed for cells grown in the presence of trimethylamine oxide, dimethylsulfoxide and disodium thiosulfate, showing that the system of S. oneidensis is efficient for heterologous expression of algal [Fe-Fe] hydrogenase. Conclusion In the present work a new efficient system for heterologous expression and maturation of C. reinhardtii hydrogenase has been developed. HydA1 of C. reinhardtii was purified and shown to contain 6 Fe atoms/molecule of protein, as expected. Using DMSO, TMAO or thiosulfate as substrates for anaerobic respiration during the cell growth, 0.4 – 0.5 mg l-1(OD600 = 1 of catalytically active HydA1 was obtained with hydrogen evolution rate of ~700 μmol H2 mg-1 min-1.

  19. Liquid metals for solar power systems

    Science.gov (United States)

    Flesch, J.; Niedermeier, K.; Fritsch, A.; Musaeva, D.; Marocco, L.; Uhlig, R.; Baake, E.; Buck, R.; Wetzel, T.

    2017-07-01

    The use of liquid metals in solar power systems is not new. The receiver tests with liquid sodium in the 1980s at the Plataforma Solar de Almería (PSA) already proved the feasibility of liquid metals as heat transfer fluid. Despite the high efficiency achieved with that receiver, further investigation of liquid metals in solar power systems was stopped due to a sodium spray fire. Recently, the topic has become interesting again and the gained experience during the last 30 years of liquid metals handling is applied to the concentrated solar power community. In this paper, recent activities of the Helmholtz Alliance LIMTECH concerning liquid metals for solar power systems are presented. In addition to the components and system simulations also the experimental setup and results are included.

  20. Thermodynamic modeling of the Sr-Co-Fe-O system

    DEFF Research Database (Denmark)

    Zhang, Wei Wei; Povoden-Karadeniz, Erwin; Chen, Ming

    2016-01-01

    This paper reviews and assesses phase equilibria and thermodynamic properties of phases in the Sr-Co-Fe-O system, with a focus on oxides, especially the SrCo1 - xFexO3 - δ perovskite. In our work, the SrCo1 - xFexO3 - δ perovskite was modeled with a three-sublattice model, where the three...... sublattices correspond to the A, B and oxygen sites in an ABO3 perovskite, respectively. A number of other important ternary oxide phases in Sr-Co-O and Sr-Co-Fe-O were also considered. Available thermodynamic and phase diagram data were carefully assessed. A thermodynamic description of Sr-Co-O was derived...... using the CALPHAD approach and was further extrapolated to that of Sr-Co-Fe-O. The thermodynamic database of Sr-Co-Fe-O established in this work allows for calculating phase diagrams, thermodynamic properties, cation distribution and defect chemistry properties, and therefore enables material...

  1. Experimental and thermodynamic assessments of substitutions in the AlFeSi, FeMnSi, FeSiZr and AlCaFeSi systems (65 wt % Si) - solidification simulation

    Energy Technology Data Exchange (ETDEWEB)

    Gueneau, C. [CEA Centre d`Etudes de Saclay, 91 - Gif-sur-Yvette (France). Dept. des Procedes d`Enrichissement]|[Paris-11 Univ., 91 - Orsay (France)]|[Compagnie de Produits Chimiques et Electrometallurgiques Pechiney, 74 - Passy-Chedde (France). Lab. Graphitation; Servant, C. [Paris-11 Univ., 91 - Orsay (France); Ansara, I. [Ecole Nationale Superieure d`Electrochimie et d`Electrometallurgie, 38 - Grenoble (France)

    1994-12-31

    The substitutions of Al <-> Si, Fe <-> Mn and Fe <-> Zr in some intermetallic compounds of the Al-Fe-Si, Fe-Mn-Si and Fe-Si-Zr systems are modelled in the Si-rich corner using a two sublattice model. The solidification paths of the studied alloys are determined at equilibrium. The ascalculated phase volume fractions of the alloys are compared to the experimental ones. Finally, a solidification simulation using the Gulliver-Scheil`s model is performed in order to explain the formation of some precipitates experimentally observed. (authors). 14 figs., 19 refs.

  2. Role of Fe-Oxidizing Bacteria in Metal Bio-Corrosion in the Marine Environment

    Science.gov (United States)

    2015-06-30

    using a variety of culture- independent and cultivation-based approaches. These include fluorescent in situ hybridization ( FISH ) using primers...laboratory. This system allowed control of Oj levels, pH , flow rates, and supplemental iron additions, and was designed so steel coupons could be...this project, we also conducted a study that investigated salinity effects on populations of marine and freshwater FeOB, showing that

  3. Adsorption of tetracycline on Fe (hydr)oxides: effects of pH and metal cation (Cu2+, Zn2+ and Al3+) addition in various molar ratios

    Science.gov (United States)

    Hsu, Liang-Ching; Liu, Yu-Ting; Syu, Chien-Hui; Huang, Mei-Hsia; Teah, Heng Yi

    2018-01-01

    Iron (Fe) (hydr)oxides control the mobility and bioavailability of tetracycline (TC) in waters and soils. Adsorption of TC on Fe (hydr)oxides is greatly affected by polyvalent metals; however, impacts of molar metal/TC ratios on TC adsorptive behaviours on Fe (hydr)oxides remain unclear. Results showed that maximum TC adsorption on ferrihydrite and goethite occurred at pH 5–6. Such TC adsorption was generally promoted by the addition of Cu2+, Zn2+ and Al3+. The greatest increase in TC adsorption was found in the system with molar Cu/TC ratio of 3 due to the formation of Fe hydr(oxide)–Cu–TC ternary complexes. Functional groups on TC that were responsible for the complexation with Cu2+shifted from phenolic diketone groups at Cu/TC molar ratio adsorption at a molar Al/TC ratio of 1. However, TC adsorption decreased for Al/TC molar ratio > 1 as excess Al3+ led to the competitive adsorption with Al/TC complexes. For the Zn2+ addition, no significant correlation was found between TC adsorption capacity and molar Zn/TC ratios. PMID:29657795

  4. Magnetic phase diagram of the Fe-Ni system

    Energy Technology Data Exchange (ETDEWEB)

    Xiong, W., E-mail: wxiong@yahoo.com [Division of Computational Thermodynamics, Department of Materials Science and Engineering, KTH (Royal Institute of Technology), Brinellvaegen 23, SE-100 44 Stockholm (Sweden); State Key Lab of Powder Metallurgy, Central South University, Changsha 410083 (China); Zhang, H.; Vitos, L. [Division of Applied Physics, Department of Materials Science and Engineering, KTH (Royal Institute of Technology), Brinellvaegen 23, SE-100 44 Stockholm (Sweden); Selleby, M. [Division of Computational Thermodynamics, Department of Materials Science and Engineering, KTH (Royal Institute of Technology), Brinellvaegen 23, SE-100 44 Stockholm (Sweden)

    2011-01-15

    Magnetic phase diagrams of body-centered cubic and face-centered cubic Fe-Ni alloys were constructed using available experimental data and ab initio calculations. The results show that significant improvements in the 'standard' diagrams (handbooks and CALPHAD databases) are required. The present work demonstrates that the CALPHAD magnetic model is not sophisticated enough to describe the Fe-Ni system. In addition, a new thermodynamic description of the lattice stability for pure Ni is urgently needed, since the recommended magnetic properties for CALPHAD modeling are distinct from the experimental and ab initio results. This work indicates that the construction of magnetic phase diagrams is indispensable during the phase transformation study of magnetic systems.

  5. Fe-based bulk metallic glasses with a larger supercooled liquid region and high ductility

    Energy Technology Data Exchange (ETDEWEB)

    Qiu, K.Q. [School of Materials Science and Engineering, Shenyang University of Technology, Shenyang 110178 (China)], E-mail: kqqiu@yahoo.com.cn; Pang, J.; Ren, Y.L.; Zhang, H.B. [School of Materials Science and Engineering, Shenyang University of Technology, Shenyang 110178 (China); Ma, C.L.; Zhang, T. [School of Materials Science and Engineering, Beijing University of Aeronautics and Astronautics, Beijing 100083 (China)

    2008-12-20

    Bulk metallic glasses (BMGs) with compositions of Fe{sub 61.5-x}Co{sub 3}Mo{sub 14}C{sub 15}B{sub 6}Er{sub 0.5}M{sub x} (x = 2, 3; M = Ni, Nb) were fabricated by copper mold casting using raw industrial materials. The X-ray diffraction (XRD), differential scanning calorimetry (DSC), mechanical tester and scanning electron microscope (SEM) were employed to check the phase constituent, the thermal stability, the mechanical properties and the fracture surfaces of as-cast samples. The results indicate that the BMGs with diameters of 1.5-3 mm were fabricated for the alloys investigated. The largest supercooled liquid region (SLR) up to 76 K was found for Fe{sub 58.5}Co{sub 3}Mo{sub 14}C{sub 15}B{sub 6}Er{sub 0.5}Ni{sub 3} BMG. The BMGs with Ni addition exhibit not only high fracture strengths reaching 3770 MPa for x = 2 and 3980 MPa for x = 3 alloys, respectively, but also apparently plastic strains up to 0.67% and 0.93%, respectively. The fracture surfaces of the Fe{sub 61.5-x}Co{sub 3}Mo{sub 14}C{sub 15}B{sub 6}Er{sub 0.5}Ni{sub x} (x = 2, 3) alloys with plasticity show narrow ridges characteristic of venous patterns combining with tearing flow between the ridges. While the Nb containing alloys show not only a lower SLR below 60 K but also a lower stress below 2400 MPa, as well as almost no plastic strain before fracture.

  6. Micromirror with large-tilting angle using Fe-based metallic glass.

    Science.gov (United States)

    Lee, Jae-Wung; Lin, Yu-Ching; Kaushik, Neelam; Sharma, Parmanand; Makino, Akihiro; Inoue, Akihisa; Esashi, Masayoshi; Gessner, Thomas

    2011-09-01

    For enhancing the micromirror properties like tilting angle and stability during actuation, Fe-based metallic glass (MG) was applied for torsion bar material. A micromirror with mirror-plate diameter of 900 μm and torsion bar dimensions length 250 μm, width 30 μm and thickness 2.5 μm was chosen for the tilting angle tests, which were performed by permanent magnets and electromagnet setup. An extremely large tilting angle of over -270° was obtained from an activation test by permanent magnet that has approximately 0.2 T of magnetic strength. A large mechanical tilting angle of over -70° was obtained by applying approximately 1.1 mT to the mirror when 93 mAwas applied to solenoid setup. The large-tilting angle of the micromirror is due to the torsion bar, which was fabricated with Fe-based MG thin film that has large elastic strain limit, fracture toughness, and excellent magnetic property.

  7. Topotactic Metal-Insulator Transition in Epitaxial SrFeOx Thin Films.

    Science.gov (United States)

    Khare, Amit; Shin, Dongwon; Yoo, Tae Sup; Kim, Minu; Kang, Tae Dong; Lee, Jaekwang; Roh, Seulki; Jung, In-Ho; Hwang, Jungseek; Kim, Sung Wng; Noh, Tae Won; Ohta, Hiromichi; Choi, Woo Seok

    2017-10-01

    Topotactic phase transformation enables structural transition without losing the crystalline symmetry of the parental phase and provides an effective platform for elucidating the redox reaction and oxygen diffusion within transition metal oxides. In addition, it enables tuning of the emergent physical properties of complex oxides, through strong interaction between the lattice and electronic degrees of freedom. In this communication, the electronic structure evolution of SrFeO x epitaxial thin films is identified in real-time, during the progress of reversible topotactic phase transformation. Using real-time optical spectroscopy, the phase transition between the two structurally distinct phases (i.e., brownmillerite and perovskite) is quantitatively monitored, and a pressure-temperature phase diagram of the topotactic transformation is constructed for the first time. The transformation at relatively low temperatures is attributed to a markedly small difference in Gibbs free energy compared to the known similar class of materials to date. This study highlights the phase stability and reversibility of SrFeO x thin films, which is highly relevant for energy and environmental applications exploiting the redox reactions. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  8. Measurement of the electron capture probabilities of55Fe with a metallic magnetic calorimeter.

    Science.gov (United States)

    Loidl, M; Rodrigues, M; Mariam, R

    2018-04-01

    The ratios of the electron capture probabilities P K , P L and P M of 55 Fe have been measured with a metallic magnetic calorimeter, a specific type of cryogenic detector. The 55 Fe source was enclosed in the detector absorber, whose dimensions were chosen such that the detection efficiency for Mn K X-rays was larger than 99.99%. Since all electrons and photons emitted by the source are absorbed in the detector, the detection efficiency is virtually 100% for K, L and M captures. The energy threshold was low enough to allow for clear separation of the M captures (~ 80eV) from noise. The capture probability ratios were translated to capture probabilities using the recommended value for the probability of the undetected N captures. The resulting values are in agreement both with the recommended values of P K , P L and P M and with the experimental data of Pengra and coworkers. Copyright © 2017 Elsevier Ltd. All rights reserved.

  9. Fe/N/C hollow nanospheres by Fe(iii)-dopamine complexation-assisted one-pot doping as nonprecious-metal electrocatalysts for oxygen reduction

    Science.gov (United States)

    Zhou, Dan; Yang, Liping; Yu, Linghui; Kong, Junhua; Yao, Xiayin; Liu, Wanshuang; Xu, Zhichuan; Lu, Xuehong

    2015-01-01

    In this work, a series of hollow carbon nanospheres simultaneously doped with N and Fe-containing species are prepared by Fe3+-mediated polymerization of dopamine on SiO2 nanospheres, carbonization and subsequent KOH etching of the SiO2 template. The electrochemical properties of the hollow nanospheres as nonprecious-metal electrocatalysts for oxygen reduction reaction (ORR) are characterized. The results show that the hollow nanospheres with mesoporous N-doped carbon shells of ~10 nm thickness and well-dispersed Fe3O4 nanoparticles prepared by annealing at 750 °C (Fe/N/C HNSs-750) exhibit remarkable ORR catalytic activity comparable to that of a commercial 20 wt% Pt/C catalyst, and high selectivity towards 4-electron reduction of O2 to H2O. Moreover, it displays better electrochemical durability and tolerance to methanol crossover effect in an alkaline medium than the Pt/C. The excellent catalytic performance of Fe/N/C HNSs-750 towards ORR can be ascribed to their high specific surface area, mesoporous morphology, homogeneous distribution of abundant active sites, high pyridinic nitrogen content, graphitic nitrogen and graphitic carbon, as well as the synergistic effect of nitrogen and iron species for catalyzing ORR.In this work, a series of hollow carbon nanospheres simultaneously doped with N and Fe-containing species are prepared by Fe3+-mediated polymerization of dopamine on SiO2 nanospheres, carbonization and subsequent KOH etching of the SiO2 template. The electrochemical properties of the hollow nanospheres as nonprecious-metal electrocatalysts for oxygen reduction reaction (ORR) are characterized. The results show that the hollow nanospheres with mesoporous N-doped carbon shells of ~10 nm thickness and well-dispersed Fe3O4 nanoparticles prepared by annealing at 750 °C (Fe/N/C HNSs-750) exhibit remarkable ORR catalytic activity comparable to that of a commercial 20 wt% Pt/C catalyst, and high selectivity towards 4-electron reduction of O2 to H2O

  10. 2D electron systems: Metals in flatland

    Science.gov (United States)

    Annett, James F.

    2012-01-01

    Is it possible for a metal to exist in a strictly two-dimensional system? This may seem trivial, but it is actually a longstanding problem. The electrical characteristics of an array of superconducting islands on a normal metal suggests that the answer could be 'yes'.

  11. Presence of Fe3+ and Zn2+ promoted biotransformation of Cd-citrate complex and removal of metals from solutions.

    Science.gov (United States)

    Qian, Jun-Wei; Tao, Yong; Zhang, Wen-Jie; He, Xiao-Hong; Gao, Ping; Li, Da-Ping

    2013-12-15

    The promotion to Cd-citrate complex biotransformation via addition of Fe(3+) and Zn(2+) was investigated. Single Fe(III)- or Zn-citrate complex was completely degraded by Pseudomonas sp. MBR, Cd-citrate complex was not. In the Cd-citrate media with molar ratio of 1:2 and 1:3, pH increase obtained from the metabolism of excess citrate slightly promoted the biotransformation of Cd-citrate complex, Cd remained in solutions. The presence of Fe(3+) and Zn(2+) resulted in complete biotransformation of Cd-citrate complex in the 1:1:2 Fe:Cd:citrate and Zn:Cd:citrate and 1:1:1:3 Fe:Zn:Cd:citrate media. Alkaline pH obtained from biotransformation of metal-citrate complexes caused almost complete removal of metals (>98%) through precipitation and co-precipitation. Pseudomonas sp. MBR potentially could be used to treat wastewater containing mixed citrate complexes of Fe(III), Zn and Cd. Copyright © 2013 Elsevier B.V. All rights reserved.

  12. CHEMICAL EVOLUTION OF THE INNER 2 DEGREES OF THE MILKY WAY BULGE: [α/Fe] TRENDS AND METALLICITY GRADIENTS

    International Nuclear Information System (INIS)

    Ryde, N.; Schultheis, M.; Grieco, V.; Matteucci, F.; Rich, R. M.; Uttenthaler, S.

    2016-01-01

    The structure, formation, and evolution of the Milky Way bulge is a matter of debate. Important diagnostics for discriminating between models of bulge formation and evolution include α-abundance trends with metallicity, and spatial abundance and metallicity gradients. Due to the severe optical extinction in the inner Bulge region, only a few detailed investigations of this region have been performed. Here we aim at investigating the inner 2 degrees of the Bulge (projected galactocentric distance of approximately 300 pc), rarely investigated before, by observing the [α/Fe] element trends versus metallicity, and by trying to derive the metallicity gradient in the b < 2° region. [α/Fe] and metallicities have been determined by spectral synthesis of 2 μm spectra of 28 M-giants in the Bulge, lying along the southern minor axis at (l, b) = (0, 0), (0, −1°), and (0, −2°). These were observed with the CRIRES spectrometer at the Very Large Telescope, (VLT) at high spectral resolution. Low-resolution K-band spectra, observed with the ISAAC spectrometer at the VLT, are used to determine the effective temperature of the stars. We present the first connection between the Galactic center (GC) and the Bulge using similar stars, high spectral resolution, and analysis techniques. The [α/Fe] trends in all our three fields show a large similarity among each other and with trends further out in the Bulge. All point to a rapid star formation episode in the Bulge. We find that there is a lack of an [α/Fe] gradient in the Bulge all the way into the center, suggesting a homogeneous Bulge when it comes to the enrichment process and star formation history. We find a large range of metallicities from −1.2 < [Fe/H] < +0.3, with a lower dispersion in the GC: −0.2 < [Fe/H] < +0.3. The derived metallicities of the stars in the three fields get, in the mean, progressively higher the closer to the Galactic plane they lie. We could interpret this as a continuation of the

  13. On the existence of the Fe sub 2 Nb sub 3 phase in the Fe-Nb system

    Energy Technology Data Exchange (ETDEWEB)

    Zelaya Bejarano, J.M. (Centro de Tecnologia, Universidade Estadual de Campinas, SP (Brazil)); Gama, S.; Ribeiro, C.A. (Instituto de Fisica Gleb Wataghin, Universidade Estadual de Campinas, SP (Brazil)); Effenberg, G. (Max-Planck-Inst. fuer Metallforschung, Inst. fuer Werkstoffwissenschaften, PML, Stuttgart (Germany)); Santos, C.

    1991-08-01

    The niobium-rich part of the Fe-Nb system has been investigated using metallography, electron microprobe, differential thermal analysis and the examination of diffusion couples. The phase relations are partially presented in the niobium-rich composition range of the phase diagram. It is concluded that the Fe{sub 2}Nb{sub 3} phase is not an equilibrium phase of the system, but appears metastable during slow cooling processes. (orig.).

  14. Novel application of a Fe-Zn double-metal cyanide catalyst in the synthesis of biodegradable, hyperbranched polymers.

    Science.gov (United States)

    Sebastian, Joby; Srinivas, Darbha

    2011-10-07

    The use of Fe-Zn double-metal cyanide as a solid catalyst for synthesizing biodegradable, hyperbranched polymers from diacids and glycerol has been reported, for the first time, wherein acidity, micro-mesoporosity and hydrophobicity of the catalyst played an important role in controlling gelation. This journal is © The Royal Society of Chemistry 2011

  15. KF-loaded mesoporous Mg-Fe bi-metal oxides: high performance transesterification catalysts for biodiesel production.

    Science.gov (United States)

    Tao, Guiju; Hua, Zile; Gao, Zhe; Zhu, Yan; Zhu, Yan; Chen, Yu; Shu, Zhu; Zhang, Lingxia; Shi, Jianlin

    2013-09-21

    Using newly developed mesoporous Mg-Fe bi-metal oxides as supports, a novel kind of high performance transesterification catalysts for biodiesel production has been synthesized. More importantly, the impregnation solvent was for the first time found to substantially affect the structures and catalytic performances of the resultant transesterification catalysts.

  16. Influence of short-range atomic order on mechanical properties of metallic glasses Fe80-XNiXB20

    NARCIS (Netherlands)

    Bengus, V.Z.; Korolkova, E.B.; Duhaj, P.; Diko, P.; Ocelik, V.; Tabachnikova, E.D.

    1990-01-01

    Variation of the chemical composition of Fe80-xNixB20 metallic glasses causes changes of the short-range atomic order and of some thermodynamic characteristics leading to nonmonotonic change of the ductile shear fracture normal stress σf under tension at 300 and 77 K. σf is maximal at xEQ30 and

  17. Giant magnetoresistance in the half-metallic double-perovskite ferrimagnet Mn2FeReO6.

    Science.gov (United States)

    Li, Man-Rong; Retuerto, Maria; Deng, Zheng; Stephens, Peter W; Croft, Mark; Huang, Qingzhen; Wu, Hui; Deng, Xiaoyu; Kotliar, Gabriel; Sánchez-Benítez, Javier; Hadermann, Joke; Walker, David; Greenblatt, Martha

    2015-10-05

    The first transition-metal-only double perovskite compound, Mn(2+) 2 Fe(3+) Re(5+) O6 , with 17 unpaired d electrons displays ferrimagnetic ordering up to 520 K and a giant positive magnetoresistance of up to 220 % at 5 K and 8 T. These properties result from the ferrimagnetically coupled Fe and Re sublattice and are affected by a two-to-one magnetic-structure transition of the Mn sublattice when a magnetic field is applied. Theoretical calculations indicate that the half-metallic state can be mainly attributed to the spin polarization of the Fe and Re sites. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  18. Temperature stimulates charge carriers in Ce0.90Fe0.1O2 for semiconductor to metal phase

    Science.gov (United States)

    Parveen, Mubeena; Saravanan, G.; Asvini, V.; Ravichandran, K.; Kalaiselvi, D.

    2018-04-01

    Ce0.90Fe0.1O2, cubic structure exhibits interesting electrical property-due to the effects of oxygen vacancies. Electrical response of nanocrystalline Ce0.90Fe0.1O2 material as a function of temperature was investigated using impedance spectroscopy. A change was observed in Nyquist plot for the temperature 903k, which has been analysed in terms of localized and delocalized electrons. An interesting behaviour of temperature stimulate semiconductor to metal like transition was observed in frequency dependent dielectric constant (ɛ') and frequency dependent dielectric loss(tan δ). Frequency dependence on the real and imaginary part of impedence with respect to temperature aids the presences of semiconductor to metal like transition in Ce0.90Fe0.1O2.

  19. The structural and magnetic properties of Fe/native-oxide systems resolved by x-ray scattering and spectroscopy methods

    Energy Technology Data Exchange (ETDEWEB)

    Couet, Sebastien

    2008-12-15

    Since the discovery of the giant magnetoresistance (GMR) effect in metallic magnetic multilayers and its industrial application in magnetic read heads, the data storage density and reading speed of hard disks steadily increased. But now the point is reached where conventional conductive multilayer structures suffer from parasitic eddy currents which decrease the signal to noise ratio of the system. To tackle this problem, new classes of materials have to be studied. One approach is to introduce ultra thin oxide layers in a metallic iron structure to reduce the conductivity while keeping a high net magnetization. This can be achieved by alternating metal deposition and controlled oxidation to produce metal/metal-oxide multilayers. However, the magnetic structure that forms in such multilayer is still rather unexplored. The aim of this work was to achieve a better understanding of the magnetic structure that forms in such iron/native-oxide multilayers. For that purpose, X-ray and neutron scattering experiments were carried out to determine the magnetic structure and its evolution in ex-situ and in-situ experiments, respectively. It was found that a non-collinear magnetic coupling appears between the metal layers, which is mediated by the antiferromagnetically ordered oxide layer in between. The use of isotope sensitive scattering techniques (namely nuclear resonant scattering and neutron reflectometry) allowed to resolve the magnetic depth profile of the system, showing that the buried oxide carries a net magnetic moment. The chemical and magnetic structure of the buried oxide was studied by in-situ X-ray absorption spectroscopy and nuclear resonant scattering. After oxidation, the layer exhibits a mixture of different oxide phases and incorporates 10 to 15% of Fe with metallic character. Upon deposition of only one atomic layer of metallic Fe, the layer reduces to a single phase FeO-like oxide. This structural change does not lead to a magnetically ordered oxide

  20. The structural and magnetic properties of Fe/native-oxide systems resolved by x-ray scattering and spectroscopy methods

    International Nuclear Information System (INIS)

    Couet, Sebastien

    2008-12-01

    Since the discovery of the giant magnetoresistance (GMR) effect in metallic magnetic multilayers and its industrial application in magnetic read heads, the data storage density and reading speed of hard disks steadily increased. But now the point is reached where conventional conductive multilayer structures suffer from parasitic eddy currents which decrease the signal to noise ratio of the system. To tackle this problem, new classes of materials have to be studied. One approach is to introduce ultra thin oxide layers in a metallic iron structure to reduce the conductivity while keeping a high net magnetization. This can be achieved by alternating metal deposition and controlled oxidation to produce metal/metal-oxide multilayers. However, the magnetic structure that forms in such multilayer is still rather unexplored. The aim of this work was to achieve a better understanding of the magnetic structure that forms in such iron/native-oxide multilayers. For that purpose, X-ray and neutron scattering experiments were carried out to determine the magnetic structure and its evolution in ex-situ and in-situ experiments, respectively. It was found that a non-collinear magnetic coupling appears between the metal layers, which is mediated by the antiferromagnetically ordered oxide layer in between. The use of isotope sensitive scattering techniques (namely nuclear resonant scattering and neutron reflectometry) allowed to resolve the magnetic depth profile of the system, showing that the buried oxide carries a net magnetic moment. The chemical and magnetic structure of the buried oxide was studied by in-situ X-ray absorption spectroscopy and nuclear resonant scattering. After oxidation, the layer exhibits a mixture of different oxide phases and incorporates 10 to 15% of Fe with metallic character. Upon deposition of only one atomic layer of metallic Fe, the layer reduces to a single phase FeO-like oxide. This structural change does not lead to a magnetically ordered oxide

  1. Metal organic frameworks as a drug delivery system for flurbiprofen

    Directory of Open Access Journals (Sweden)

    AL Haydar M

    2017-09-01

    Full Text Available Muder AL Haydar,1,2 Hussein Rasool Abid,3,4 Bruce Sunderland,2 Shaobin Wang5,6 1Pharmaceutics Department, College of the Pharmacy, University of Kerbala, Kerbala, Iraq; 2Pharmaceutics Department, School of Pharmacy, Faculty of Health Sciences, Curtin University, Perth, WA, Australia; 3Department of Chemical Engineering, Curtin University, Perth, WA, Australia; 4College of Applied Medical Sciences, University of Kerbala, Kerbala, Iraq; 5School of Pharmacy, Faculty of Health Sciences, Curtin University, Perth, WA, Australia; 6Department of Chemical Engineering, School of Chemical and Petroleum Engineering, Faculty of Science and Engineering, Curtin University, Perth, WA, Australia Background: Metal organic frameworks (MOFs have attracted more attention in the last decade because of a suitable pore size, large surface area, and high pore volume. Developing biocompatible MOFs such as the MIL family as a drug delivery system is possible. Purpose: Flurbiprofen (FBP, a nonsteroidal anti-inflammatory agent, is practically insoluble in aqueous solution, and, therefore, needs suitable drug delivery systems. Different biocompatible MOFs such as Ca-MOF and Fe-MILs (53, 100, and 101 were synthesized and employed for FBP delivery. Patients and methods: A sample of 50 mg of each MOF was mixed and stirred for 24 h with 10 mL of 5 mg FBP in acetonitrile (40% in a sealed container. The supernatant of the mixture after centrifuging was analyzed by high-performance liquid chromatography to determine the loaded quantity of FBP on the MOF. The overnight-dried solid material after centrifuging the mixture was analyzed for loading percent using X-ray diffraction, Fourier-transform infrared spectroscopy, scanning electron microscopy, nuclear magnetic resonance, and FBP release profile. Results: The loading values of FBP were achieved at 10.0%±1%, 20%±0.8%, 37%±2.3%, and 46%±3.1% on Ca-MOF, Fe-MIL-53, Fe-MIL-101, and Fe-MIL-100, respectively. The FBP release

  2. Slowing down of 1.3-3.5 MeV/u Fe, Kr and I ions in ten metals

    CERN Document Server

    Alanko, T; Kylloenen, V; Müller, S; Raeisaenen, J; Virtanen, A

    2000-01-01

    Stopping powers for 1.3-3.5 MeV/u sup 5 sup 6 Fe, sup 8 sup 0 sup , sup 8 sup 4 Kr and sup 1 sup 2 sup 7 I ions in Mg, V, Fe, Co, Ni, Cu, Nb, Sn, Ta and Au have been determined by a transmission technique exposing the metallic sample foils to the direct ion beam. No previous data have been published for Mg, V, Fe, Co, Nb, Sn or Ta stopping media with these ion energies. The experimental results are compared with parametrizations of the stopping powers found in the literature (SRIM-2000 and Hubert's parametrization). Discrepancies as high as 21 and 16% are observed for SRIM and Hubert's parametrization, respectively. However, there is agreement between the present results and other experimental data available at corresponding ion velocities for sup 8 sup 4 Kr and sup 5 sup 6 Fe in Ni, Cu, and Au.

  3. A thermodynamic evaluation of the Fe-Nb system

    International Nuclear Information System (INIS)

    Srikanth, S.; Petric, A.

    1994-01-01

    An optimised set of thermodynamic functions consistent with the phase diagram was derived for the Fe-Nb system from information on phase equilibria and thermodynamic data available in the literature. The thermodynamic properties of the intermediate ε (Fe 2 Nb) phase were described using the sublattice model. A Redlich-Kister equation was used to describe the excess thermodynamic functions of the liquid, bcc and fcc phases. For the μ phase, the enthalpy of formation was estimated from Miedema's model. The interaction coefficients were evaluated using an optimisation procedure employing a conjugate gradient method. The phase diagram and the thermodynamic functions calculated from the evaluated parameters are in good agreement with experimental data. (orig.)

  4. Experimental Study of Liquidus of the "FeO"-SiO2-PbO Slags in Equilibrium with Air and with Metallic Lead

    Science.gov (United States)

    Shevchenko, Maksym; Hidayat, Taufiq; Hayes, Peter C.; Jak, Evgueni

    Limited data are available on phase equilibria of the "FeO"-SiO2-PbO slag system at conditions used in the lead smelting due to difficulties from lead vaporization and interactions with metal and ceramic crucibles. Recently experimental procedures have been developed and successfully applied to complex industrial slag-metal-matte systems involving high temperature equilibration on a primary phase substrate and rapid quenching followed by the electron probe X-ray microanalysis. The liquidus isotherms and invariant lines in the "FeO"-SiO2-PbO slag system in equilibrium with air and with metallic lead have been constructed. Preliminary data compared to the FactSage package predictions demonstrate differences in some aspects, indicating the possibility for further improvement of the thermodynamic database. The present work is a part of the integrated experimental and thermodynamic modelling research program on multi-phase lead systems in support of the optimization and development of complex lead smelting, refining and recycling technologies.

  5. Photoluminescence and semiconducting behavior of Fe, Co, Ni and Cu implanted in heavy metal oxide glasses

    Directory of Open Access Journals (Sweden)

    Mohamed A. Marzouk

    2016-07-01

    Full Text Available Transition metal ions (0.5 wt% of Fe2O3, CoO, NiO or CuO doped heavy metal oxide glasses having chemical composition of 60PbO·20Bi2O3·20 MxOy mol% (where MxOy = B2O3 or SiO2 or P2O5 were prepared by conventional melt annealing method. Combined optical and photoluminescence properties have been measured and employed to evaluate the prepared glassy samples. From the absorption edge data, the values of the optical band gap Eopt, Urbach energy (ΔE and refractive index were calculated to estimate semiconducting behavior. Photoluminescence and values of the optical energy gap were found to be dependent on the glass composition. The variations of the photoluminescence intensity, values of optical band gap, Urbach energy and refractive index gave an indication to use the prepared glasses for design of novel functional optical materials with higher optical performance.

  6. IR thermographic observation and shear bands plasticity analysis in Fe-based metallic glass

    International Nuclear Information System (INIS)

    Bouzakher, B.; Benameur, T.; Sidhom, H.

    2009-01-01

    Infrared thermography observation and in situ atomic force microscopy characterization were carried out to investigate the mechanical damage processes at the edge-notch region of large ribbons of Fe 78 Si 10 B 12 metallic glass. An obvious thermoelastic and inelastic degradation phenomenon was observed ahead at the notched region of the specimens, which probably result from free volume accumulation process and shear band activity during plane stress solicitations. Moreover, AFM topographic and frictional analysis of changes in the crack path during stable crack propagation regime revealed a periodic morphology evolution, formation of nanoscale damage cavity in the range of 20-140 nm and a maximum temperature rise ahead of the pre-crack tip was found in the order of 1.5 deg. C. The nanometer scaled shear offset, discreteness and shear bands density were determined. While these key parameters play a role in observing a large plastic zone in front of the crack, however they are unable to explain the distinct intrinsic ductility of some monolithic metallic glasses. A general Mohr-Coulomb-type constitutive description was used to deduce analytic expressions for prediction of the variation of hydrostatic component of the applied stress to the shear stress ratio as function of Poisson's ratio.

  7. Enhancement effects of reducing agents on the degradation of tetrachloroethene in the Fe(II)/Fe(III) catalyzed percarbonate system

    International Nuclear Information System (INIS)

    Miao, Zhouwei; Gu, Xiaogang; Lu, Shuguang; Brusseau, Mark L.; Yan, Ni; Qiu, Zhaofu; Sui, Qian

    2015-01-01

    Highlights: • PCE degradation by reducing-agent modified Fe-catalyzed percarbonate was studied. • The addition of reducing agents significantly increased PCE degradation. • Hydroxylamine hydrochloride showed the best effect on enhancing PCE degradation. • The primary PCE degradation mechanism was oxidation by hydroxyl radical. • O 2 · − participated in the degradation of PCE in reducing-agent modified system. - Abstract: In this study, the effects of reducing agents on the degradation of tetrachloroethene (PCE) were investigated in the Fe(II)/Fe(III) catalyzed sodium percarbonate (SPC) system. The addition of reducing agents, including hydroxylamine hydrochloride, sodium sulfite, ascorbic acid and sodium ascorbate, accelerated the Fe(III)/Fe(II) redox cycle, leading to a relatively steady Fe(II) concentration and higher production of free radicals. This, in turn, resulted in enhanced PCE oxidation by SPC, with almost complete PCE removal obtained for appropriate Fe and SPC concentrations. The chemical probe tests, using nitrobenzene and carbon tetrachloride, demonstrated that HO· was the predominant radical in the system and that O 2 · − played a minor role, which was further confirmed by the results of electron spin resonance measurements. PCE degradation decreased significantly with the addition of isopropanol, a HO· scavenger, supporting the hypothesis that HO· was primarily responsible for PCE degradation. It is noteworthy that Cl − release was slightly delayed in the first 20 min, indicating that intermediate products were produced. However, these intermediates were further degraded, resulting in the complete conversion of PCE to CO 2 . In conclusion, the use of reducing agents to enhance Fe(II)/Fe(III) catalyzed SPC oxidation appears to be a promising approach for the rapid degradation of organic contaminants in groundwater.

  8. Enhancement effects of reducing agents on the degradation of tetrachloroethene in the Fe(II)/Fe(III) catalyzed percarbonate system

    Energy Technology Data Exchange (ETDEWEB)

    Miao, Zhouwei [State Environmental Protection Key Laboratory of Environmental Risk Assessment and Control on Chemical Process, East China University of Science and Technology, Shanghai 200237 (China); Soil, Water and Environmental Science Department, School of Earth and Environmental Sciences, The University of Arizona, 429 Shantz Building, Tucson, AZ 85721 (United States); Gu, Xiaogang [State Environmental Protection Key Laboratory of Environmental Risk Assessment and Control on Chemical Process, East China University of Science and Technology, Shanghai 200237 (China); Lu, Shuguang, E-mail: lvshuguang@ecust.edu.cn [State Environmental Protection Key Laboratory of Environmental Risk Assessment and Control on Chemical Process, East China University of Science and Technology, Shanghai 200237 (China); Brusseau, Mark L. [Soil, Water and Environmental Science Department, School of Earth and Environmental Sciences, The University of Arizona, 429 Shantz Building, Tucson, AZ 85721 (United States); Yan, Ni [Hydrology and Water Resources Department, School of Earth and Environmental Sciences, University of Arizona, 429 Shantz Building, Tucson, AZ 85721 (United States); Qiu, Zhaofu; Sui, Qian [State Environmental Protection Key Laboratory of Environmental Risk Assessment and Control on Chemical Process, East China University of Science and Technology, Shanghai 200237 (China)

    2015-12-30

    Highlights: • PCE degradation by reducing-agent modified Fe-catalyzed percarbonate was studied. • The addition of reducing agents significantly increased PCE degradation. • Hydroxylamine hydrochloride showed the best effect on enhancing PCE degradation. • The primary PCE degradation mechanism was oxidation by hydroxyl radical. • O{sub 2}·{sup −} participated in the degradation of PCE in reducing-agent modified system. - Abstract: In this study, the effects of reducing agents on the degradation of tetrachloroethene (PCE) were investigated in the Fe(II)/Fe(III) catalyzed sodium percarbonate (SPC) system. The addition of reducing agents, including hydroxylamine hydrochloride, sodium sulfite, ascorbic acid and sodium ascorbate, accelerated the Fe(III)/Fe(II) redox cycle, leading to a relatively steady Fe(II) concentration and higher production of free radicals. This, in turn, resulted in enhanced PCE oxidation by SPC, with almost complete PCE removal obtained for appropriate Fe and SPC concentrations. The chemical probe tests, using nitrobenzene and carbon tetrachloride, demonstrated that HO· was the predominant radical in the system and that O{sub 2}·{sup −} played a minor role, which was further confirmed by the results of electron spin resonance measurements. PCE degradation decreased significantly with the addition of isopropanol, a HO· scavenger, supporting the hypothesis that HO· was primarily responsible for PCE degradation. It is noteworthy that Cl{sup −} release was slightly delayed in the first 20 min, indicating that intermediate products were produced. However, these intermediates were further degraded, resulting in the complete conversion of PCE to CO{sub 2}. In conclusion, the use of reducing agents to enhance Fe(II)/Fe(III) catalyzed SPC oxidation appears to be a promising approach for the rapid degradation of organic contaminants in groundwater.

  9. Selective Metal Exsolution in BaFe2-yMy(PO4)2 (M = Co2+, Ni2+) Solid Solutions

    Energy Technology Data Exchange (ETDEWEB)

    Alcover, Ignacio Blazquez [Universite Lille Nord de France (France); Daviero-Minaud, Sylvie [Universite Lille Nord de France (France); David, Rénald [Universite Picardie Jules Verne (France); Filimonov, Dmitry [Moscow State Univ., Moscow (Russian Federation); Huvé, Marielle [Universite Lille Nord de France (France); Attfield, J. Paul [Univ. of Edinburgh (United Kingdom); Kabbour, Houria [Universite Lille Nord de France (France); Mentré, Olivier [Universite Lille Nord de France (France)

    2015-08-19

    The 2D-Ising ferromagnetic phase BaFe2+2(PO4)2 shows exsolution of up to one-third of its iron content (giving BaFe3+1.33(PO4)2) under mild oxidation conditions, leading to nanosized Fe2O3 exsolved clusters. Here we have prepared BaFe2–yMy(PO4)2 (M = Co2+, Ni2+; y = 0, 0.5, 1, 1.5) solid solutions to investigate the feasibility and selectivity of metal exsolution in these mixed metallic systems. For all the compounds, after 600 °C thermal treatment in air, a complete oxidation of Fe2+ to Fe3+ leaves stable M2+ ions, as verified by 57Fe Mössbauer spectroscopy, TGA, TEM, microprobe, and XANES. Furthermore, the size of the nanometric α-Fe2O3clusters coating the main phase strongly depends on the yM metal concentration. For M-rich phases the iron diffusion is hampered so that a significant fraction of superparamagnetic α-Fe2O3 particles (100% for BaFe0.5–xCo1.5(PO4)2) was detected even at 78 K. Although Ni2+and Co2+ ions tend to block Fe diffusion, the crystal structure of BaFe0.67Co1(PO4)2demonstrates a fully ordered rearrangement of Fe3+ and Co2+ ions after Fe exsolution. We found that the magnetic behaviors of the Fe-depleted materials are mostly dominated by antiferromagnetic exchange, while Co2+-rich compounds show metamagnetic transitions reminiscent of the BaCo2(PO4)2 soft helicoidal magnet.

  10. Fe-Al-Nb phase diagram investigation and directional growth of the (Fe, Al){sub 2}Nb-(Fe, Al, Nb){sub ss} eutectic system

    Energy Technology Data Exchange (ETDEWEB)

    Mota, M.A. [State University of Campinas, C.P. 6122, 13083-970 Campinas, SP (Brazil); Coelho, A.A. [State University of Campinas, C.P. 6122, 13083-970 Campinas, SP (Brazil); Bejarano, J.M.Z. [State University of Campinas, C.P. 6122, 13083-970 Campinas, SP (Brazil); Gama, S. [State University of Campinas, C.P. 6122, 13083-970 Campinas, SP (Brazil); Caram, R. [State University of Campinas, C.P. 6122, 13083-970 Campinas, SP (Brazil)]. E-mail: rcaram@fem.unicamp.br

    2005-08-16

    An attractive alternative method for the manufacture of high temperature structural materials may be achieved from a eutectic transformation found in the Fe-Al-Nb system, which generates the (Fe, Al){sub 2}Nb and (Fe, Al, Nb){sub ss} solid phases. Eutectic and off-eutectic samples from the Fe-Al-Nb system were prepared by arc melting under argon atmosphere, which were subsequently directionally solidified using a vertical Bridgman crystal growth unit. The ingots obtained were investigated using optical and electron scanning microscopy with the purpose to evaluate the effect of the growth condition on the microstructure. Primarily, the growth mode of the (Fe, Al){sub 2}Nb/(Fe, Al, Nb) eutectic was considered by examining off-eutectic samples. The solidification experiments carried out under different conditions revealed that the microstructure of this system is very sensitive to a growth rate variation. At a low growth rate, the eutectic microstructure was regular, even though several types of defects were found. As the growth rate was increased, a transition from lamellar to fibrous morphology was observed. Some aspects of this transition were also evaluated.

  11. Donnan membrane speciation of Al, Fe, trace metals and REEs in coastal lowland acid sulfate soil-impacted drainage waters

    Energy Technology Data Exchange (ETDEWEB)

    Jones, Adele M.; Xue, Youjia [School of Civil and Environmental Engineering, University of New South Wales, Sydney, NSW 2052 (Australia); Kinsela, Andrew S. [School of Civil and Environmental Engineering, University of New South Wales, Sydney, NSW 2052 (Australia); Institute for Environmental Research (IER), Australian Nuclear Science and Technology Organisation (ANSTO), Lucas Heights, NSW 2234 (Australia); Wilcken, Klaus M. [Institute for Environmental Research (IER), Australian Nuclear Science and Technology Organisation (ANSTO), Lucas Heights, NSW 2234 (Australia); Collins, Richard N., E-mail: richard.collins@unsw.edu.au [School of Civil and Environmental Engineering, University of New South Wales, Sydney, NSW 2052 (Australia)

    2016-03-15

    Donnan dialysis has been applied to forty filtered drainage waters collected from five coastal lowland acid sulfate soil (CLASS) catchments across north-eastern NSW, Australia. Despite having average pH values < 3.9, 78 and 58% of Al and total Fe, respectively, were present as neutral or negatively-charged species. Complementary isotope dilution experiments with {sup 55}Fe and {sup 26}Al demonstrated that only soluble (i.e. no colloidal) species were present. Trivalent rare earth elements (REEs) were also mainly present (> 70%) as negatively-charged complexes. In contrast, the speciation of the divalent trace metals Co, Mn, Ni and Zn was dominated by positively-charged complexes and was strongly correlated with the alkaline earth metals Ca and Mg. Thermodynamic equilibrium speciation calculations indicated that natural organic matter (NOM) complexes dominated Fe(III) speciation in agreement with that obtained by Donnan dialysis. In the case of Fe(II), however, the free cation was predicted to dominate under thermodynamic equilibrium, whilst our results indicated that Fe(II) was mainly present as neutral or negatively-charged complexes (most likely with sulfate). For all other divalent metals thermodynamic equilibrium speciation calculations agreed well with the Donnan dialysis results. The proportion of Al and REEs predicted to be negatively-charged was also grossly underestimated, relative to the experimental results, highlighting possible inaccuracies in the stability constants developed for these trivalent Me(SO{sub 4}){sub 2}{sup −} and/or Me–NOM complexes and difficulties in modeling complex environmental samples. These results will help improve metal mobility and toxicity models developed for CLASS-affected environments, and also demonstrate that Australian CLASS environments can discharge REEs at concentrations an order of magnitude greater than previously reported. - Highlights: • CLASS discharge large amounts of metals and their speciation is poorly

  12. Synchrotron X-ray microfluorescence measurement of metal distributions in Phragmites australis root system in the Yangtze River intertidal zone

    Energy Technology Data Exchange (ETDEWEB)

    Feng, Huan; Zhang, Weiguo; Qian, Yu; Liu, Wenliang; Yu, Lizhong; Yoo, Shinjae; Wang, Jun; Wang, Jia-Jun; Eng, Christopher; Liu, Chang-Jun; Tappero, Ryan

    2016-06-15

    This study investigates the distributions of Br, Ca, Cl, Cr, Cu, K, Fe, Mn, Pb, Ti, V and Zn inPhragmites australisroot system and the function of Fe nanoparticles in scavenging metals in the root epidermis using synchrotron X-ray microfluorescence, synchrotron transmission X-ray microscope measurement and synchrotron X-ray absorption near-edge structure techniques. The purpose of this study is to understand the mobility of metals in wetland plant root systems after their uptake from rhizosphere soils.Phragmites australissamples were collected in the Yangtze River intertidal zone in July 2013. The results indicate that Fe nanoparticles are present in the root epidermis and that other metals correlate significantly with Fe, suggesting that Fe nanoparticles play an important role in metal scavenging in the epidermis.

  13. Constraints on Metal Oxide and Metal Hydroxide Abundances in the Winds of AGB Stars: Potential Detection of FeO in R Dor

    Science.gov (United States)

    Decin, L.; Danilovich, T.; Gobrecht, D.; Plane, J. M. C.; Richards, A. M. S.; Gottlieb, C. A.; Lee, K. L. K.

    2018-03-01

    Using the Atacama Large Millimeter/submillimeter Array (ALMA), we observed the stellar wind of two oxygen-rich asymptotic giant branch stars, IK Tau and R Dor, between 335 and 362 GHz. One aim was to detect metal oxides and metal hydroxides (AlO, AlOH, FeO, MgO, and MgOH), some of which are thought to be direct precursors of dust nucleation and growth. We report on the potential first detection of FeO (v = 0, Ω = 4, J = 11–10) in R Dor (mass-loss rate \\dot{M} ∼ 1 × 10‑7 M ⊙ yr‑1). The presence of FeO in IK Tau (\\dot{M} ∼ 5 × 10‑6 M ⊙ yr‑1) cannot be confirmed, due to a blend with 29SiS, a molecule that is absent in R Dor. The detection of AlO in R Dor and of AlOH in IK Tau was reported earlier by Decin et al. All other metal oxides and hydroxides, as well as MgS, remain undetected. We derive a column density N(FeO) of 1.1 ± 0.9 × 1015 cm‑2 in R Dor, or a fractional abundance [FeO/H] ∼ 1.5 × 10‑8 accounting for non-local thermodynamic equilibrium effects. The derived fractional abundance [FeO/H] is a factor ∼20 larger than conventional gas-phase chemical-kinetic predictions. This discrepancy may be partly accounted for by the role of vibrationally excited OH in oxidizing Fe, or it may be evidence for other currently unrecognized chemical pathways producing FeO. Assuming a constant fractional abundance w.r.t. H2, the upper limits for the other metals are [MgO/H2] < 5.5 × 10‑10 (R Dor) and <7 × 10‑11 (IK Tau), [MgOH/H2] < 9 × 10‑9 (R Dor) and <1 × 10‑9 (IK Tau), [CaO/H2] < 2.5 × 10‑9 (R Dor) and <1 × 10‑10 (IK Tau), [CaOH/H2] < 6.5 × 10‑9 (R Dor) and <9 × 10‑10 (IK Tau), and [MgS/H2] < 4.5 × 10‑10 (R Dor) and <6 × 10‑11 (IK Tau). The retrieved upper-limit abundances for these latter molecules are in accord with the chemical model predictions.

  14. Metal-rich, Metal-poor: Updated Stellar Population Models for Old Stellar Systems

    Science.gov (United States)

    Conroy, Charlie; Villaume, Alexa; van Dokkum, Pieter G.; Lind, Karin

    2018-02-01

    We present updated stellar population models appropriate for old ages (>1 Gyr) and covering a wide range in metallicities (‑1.5 ≲ [Fe/H] ≲ 0.3). These models predict the full spectral variation associated with individual element abundance variation as a function of metallicity and age. The models span the optical–NIR wavelength range (0.37–2.4 μm), include a range of initial mass functions, and contain the flexibility to vary 18 individual elements including C, N, O, Mg, Si, Ca, Ti, and Fe. To test the fidelity of the models, we fit them to integrated light optical spectra of 41 Galactic globular clusters (GCs). The value of testing models against GCs is that their ages, metallicities, and detailed abundance patterns have been derived from the Hertzsprung–Russell diagram in combination with high-resolution spectroscopy of individual stars. We determine stellar population parameters from fits to all wavelengths simultaneously (“full spectrum fitting”), and demonstrate explicitly with mock tests that this approach produces smaller uncertainties at fixed signal-to-noise ratio than fitting a standard set of 14 line indices. Comparison of our integrated-light results to literature values reveals good agreement in metallicity, [Fe/H]. When restricting to GCs without prominent blue horizontal branch populations, we also find good agreement with literature values for ages, [Mg/Fe], [Si/Fe], and [Ti/Fe].

  15. The Effects of Strain-Annealing on Tuning Permeability and Lowering Losses in Fe-Ni-Based Metal Amorphous Nanocomposites

    Science.gov (United States)

    Aronhime, Natan; DeGeorge, Vincent; Keylin, Vladimir; Ohodnicki, Paul; McHenry, Michael E.

    2017-11-01

    Fe-Ni-based metal amorphous nanocomposites with a range of compositions (Fe100- x Ni x )80Nb4Si2B14 (30 ≤ x ≤ 70) are investigated for motor and transformer applications, where it is beneficial to have tunable permeability. It is shown that strain annealing offers an effective method for tuning permeability in these alloys. For an Fe-rich alloy, permeability increased from 4000 to 16,000 with a positive magnetostriction. In a Ni-rich alloy, permeability decreased from 290 to 40 with a negative magnetostriction. Significant elongations (above 60%) are observed during strain annealing at high stress. Crystallization products have been determined in all alloys heated to 480°C. γ-FeNi is formed in all alloys, while (Fe30Ni70)80Nb4Si2B14 also undergoes secondary crystallization at temperatures of approximately 480°C to form a phase with the Cr23C6-type structure and a likely composition of Fe21Nb2B6. Toroidal losses have been measured for (Fe70Ni30)80Nb4Si y B16- y (0 ≤ y ≤ 3) at various annealing temperatures. At an induction of 1 T and frequency of 400 Hz and 1 kHz, the toroidal losses obtained are W1.0T, 400 Hz = 0.9 W/kg and W1.0T, 1 kHz = 2.3 W/kg, respectively. These losses are lower than losses recently reported for state of the art 3.0% and 6.5% silicon steels, a Metglas Fe-based amorphous alloy, and some Fe-based nanocomposites.

  16. Response of metallic glasses Fe40Ni40P14B6 and Fe80B20 to irradiation with 800-MeV protons

    International Nuclear Information System (INIS)

    Cost, J.R.; Sommer, W.F.

    1981-01-01

    Metallic glasses with compositions of Fe 40 Ni 40 P 14 B 6 and Fe 80 B 20 were irradiated in the 800 MeV proton beam at the Los Alamos Meson Physics Facility while the electrical resistance and length changes were monitored. The resistance and the length of the first alloy were both found to increase and saturate with dose to ΔR/R approx. = 5 x 10 -3 and ΔL/L approx. = 2 x 10 -3 . For the second alloy the total dose of 1.1 x 10 19 p/cm 2 , which was calculated to give roughly 0.12 dpa, was slightly less than that required for saturation. No annealing of these increases was observed for anneals from room temperature to 250 0 C. These results are interpreted in terms of a model in which collision cascades create small regions of increased atomic disorder which fully overlap each other at saturation

  17. Development of Fe-B Based Bulk Metallic Glasses: Morphology of Residual Phases in Fe50Ni16Mo6B18Zr10 Glass

    Directory of Open Access Journals (Sweden)

    Tiburce A. Aboki

    2013-04-01

    Full Text Available Iron-boron based bulk metallic glasses (BMG development has been initiated using Fe40Ni38Mo4B18 as precursor. Addition of zirconium up to 10 atomic % along with the reduction of Ni proportion improves the glass forming ability (GFA, which is optimum when Ni is suppressed in the alloy. However melting instability occurred during the materials fabrication resulting in the formation of residual crystalline phases closely related to the amorphous phase. Microstructure study shows an evolution from amorphous structure to peculiar acicular structure, particularly for Fe50Ni16Mo6B18Zr10, suggesting the amorphous structure as interconnected atomic sheets like “atomic mille feuilles” whose growth affects the alloys’ GFA.

  18. Effects of particle size and forming pressure on pore properties of Fe-Cr-Al porous metal by pressureless sintering

    Science.gov (United States)

    Koo, Bon-Uk; Yi, Yujeong; Lee, Minjeong; Kim, Byoung-Kee

    2017-03-01

    With increased hydrogen consumption in ammonia production, refining and synthesis, fuel cells and vehicle industries, development of the material components related to hydrogen production is becoming an important factor in industry growth. Porous metals for fabrication of hydrogen are commonly known for their relative excellence in terms of large area, lightness, lower heat capacity, high toughness, and permeability. Fe-Cr-Al alloys not only have high corrosion resistance, heat resistance, and chemical stability but also ductility, excellent mechanical properties. In order to control powder size and sintering temperature effects of Fe-Cr-Al porous metal fabrication, Fe-Cr-Al powder was classified into 25-35 μm, 35-45 μm, 45-75 μm using an auto shaking sieve machine and then classified Fe-Cr-Al powders were pressed into disk shapes using a uniaxial press machine and CIP. The pelletized Fe-Cr-Al specimens were sintered at various temperatures in high vacuum. Properties such as pore size, porosity, and air permeability were evaluated using perm-porosimetry. Microstructure and phase changes were observed with SEM and XRD. Porosity and relative density were proportionated to increasing sintering temperature. With sufficient sintering at increasing temperatures, the pore size is expected to be gradually reduced. Porosity decreased with increasing sintering temperature and gradually increased necking of the powder.

  19. Fragility of the spin-glass-like collective state to a magnetic field in an interacting Fe-C nanoparticle system

    DEFF Research Database (Denmark)

    Jönsson, P. E.; Felton, S.; Svedlindh, P.

    2001-01-01

    The effect of applied magnetic fields on the collective nonequilibrium dynamics of a strongly interacting Fe-C nanoparticle system has been investigated. It is experimentally shown that the magnetic aging diminishes to finally disappear for fields of moderate strength. The field needed to remove ...... the observable aging behavior increases with decreasing temperature. The same qualitative behavior is observed in an amorphous metallic spin glass (Fe0.15Ni0.85)(75)P16B6Al3....

  20. Fe3O4/Reduced Graphene Oxide Nanocomposite: Synthesis and Its Application for Toxic Metal Ion Removal

    Directory of Open Access Journals (Sweden)

    Nguyen Thi Vuong Hoan

    2016-01-01

    Full Text Available The synthesis of reduced graphene oxide modified by magnetic iron oxide (Fe3O4/rGO and its application for heavy metals removal were demonstrated. The obtained samples were characterized by X-ray diffraction (XRD, nitrogen adsorption/desorption isotherms, X-ray photoelectron spectroscopy (XPS, Fourier transform infrared spectroscopy (FT-IR, and magnetic measurement. The results showed that the obtained graphene oxide (GO contains a small part of initial graphite as well as reduced oxide graphene. GO exhibits very high surface area in comparison with initial graphite. The morphology of Fe3O4/rGO consists of very fine spherical iron nanooxide particles in nanoscale. The formal kinetics and adsorption isotherms of As(V, Ni(II, and Pb(II over obtained Fe3O4/rGO have been investigated. Fe3O4/rGO exhibits excellent heavy metal ions adsorption indicating that it is a potential adsorbent for water sources contaminated by heavy metals.

  1. In vitro corrosion properties and cytocompatibility of Fe-Ga alloys as potential biodegradable metallic materials.

    Science.gov (United States)

    Wang, Henan; Zheng, Yang; Liu, Jinghua; Jiang, Chengbao; Li, Yan

    2017-02-01

    The in vitro biodegradable properties and cytocompatibility of Fe-Ga alloys including Fe 81 Ga 19 , (Fe 81 Ga 19 ) 98 B 2 and (Fe 81 Ga 19 ) 99.5 (TaC) 0.5 , and pure Fe were investigated for biomedical applications. The microstructure of the alloys was characterized using X-ray diffraction spectroscopy and optical microscopy. The results showed that A2 and D0 3 phases were detected for the three types of Fe-Ga alloys, and additional Fe 2 B and TaC phases were found in the (Fe 81 Ga 19 ) 98 B 2 and (Fe 81 Ga 19 ) 99.5 (TaC) 0.5 alloys, respectively. The corrosion rates of the Fe-Ga alloys were higher than that of pure Fe, as demonstrated by both potentiodynamic polarization measurements and immersion tests in simulated body fluid. The alloying element Ga lowered the corrosion potential of the Fe matrix and made it more susceptible to corrosion. Severe pitting corrosion developed on the surface of the Fe 81 Ga 19 alloy after the addition of ternary B or TaC due to the multi-phase microstructures. The MC3T3-E1 cells exhibited good adhesion and proliferation behavior on the surfaces of the Fe-Ga alloys after culture for 4h and 24h. Copyright © 2016 Elsevier B.V. All rights reserved.

  2. From which soil metal fractions Fe, Mn, Zn and Cu are taken up by olive trees (Olea europaea L., cv. 'Chondrolia Chalkidikis') in organic groves?

    Science.gov (United States)

    Chatzistathis, T; Papaioannou, A; Gasparatos, D; Molassiotis, A

    2017-12-01

    Organic farming has been proposed as an alternative agricultural system to help solve environmental problems, like the sustainable management of soil micronutrients, without inputs of chemical fertilizers. The purposes of this study were: i) to assess Fe, Mn, Zn and Cu bioavailability through the determination of sequentially extracted chemical forms (fractions) and their correlation with foliar micronutrient concentrations in mature organic olive (cv. 'Chondrolia Chalkidikis') groves; ii) to determine the soil depth and the available forms (fractions) by which the 4 metals are taken up by olive trees. DTPA extractable (from the soil layers 0-20, 20-40 and 40-60 cm) and foliar micronutrient concentrations were determined in two organic olive groves. Using the Tessier fractionation, five fractions, for all the metals, were found: exchangeable, bound to carbonates (acid-soluble), bound to Fe-Mn oxides (reducible), organic (oxidizable), as well as residual form. Our results indicated that Fe was taken up by the olive trees as organic complex, mainly from the soil layer 40-60 cm. Manganese was taken up from the exchangeable fraction (0-20 cm); Zinc was taken up as organic complex from the layers 0-20 and 40-60 cm, as well as in the exchangeable form from the upper 20 cm. Copper was taken up from the soil layers 0-20 and 40-60 cm as soluble organic complex, and as exchangeable ion from the upper 20 cm. Our data reveal the crucial role of organic matter to sustain metal (Fe, Zn and Cu) uptake -as soluble complexes-by olive trees, in mature organic groves grown on calcareous soils; it is also expected that these data will constitute a thorough insight and useful tool towards a successful nutrient and organic C management for organic olive groves, since no serious nutritional deficiencies were found. Copyright © 2017 Elsevier Ltd. All rights reserved.

  3. Metallic oxide nano-clusters synthesis by ion implantation in high purity Fe10Cr alloy

    International Nuclear Information System (INIS)

    Zheng, Ce

    2015-01-01

    ODS (Oxide Dispersed Strengthened) steels, which are reinforced with metal dispersions of nano-oxides (based on Y, Ti and O elements), are promising materials for future nuclear reactors. The detailed understanding of the mechanisms involved in the precipitation of these nano-oxides would improve manufacturing and mechanical properties of these ODS steels, with a strong economic impact for their industrialization. To experimentally study these mechanisms, an analytical approach by ion implantation is used, to control various parameters of synthesis of these precipitates as the temperature and concentration. This study demonstrated the feasibility of this method and concerned the behaviour of alloys models (based on aluminium oxide) under thermal annealing. High purity Fe-10Cr alloys were implanted with Al and O ions at room temperature. Transmission electron microscopy observations showed that the nano-oxides appear in the Fe-10Cr matrix upon ion implantation at room temperature without subsequent annealing. The mobility of implanted elements is caused by the defects created during ion implantation, allowing the nucleation of these nanoparticles, of a few nm in diameter. These nanoparticles are composed of aluminium and oxygen, and also chromium. The high-resolution experiments show that their crystallographic structure is that of a non-equilibrium compound of aluminium oxide (cubic γ-Al 2 O 3 type). The heat treatment performed after implantation induces the growth of the nano-sized oxides, and a phase change that tends to balance to the equilibrium structure (hexagonal α-Al 2 O 3 type). These results on model alloys are fully applicable to industrial materials: indeed ion implantation reproduces the conditions of milling and heat treatments are at equivalent temperatures to those of thermo-mechanical treatments. A mechanism involving the precipitation of nano-oxide dispersed in ODS alloys is proposed in this manuscript based on the obtained experimental results

  4. Magnetostrictive performance of additively manufactured CoFe rods using the LENSTM system

    Science.gov (United States)

    Jones, Nicholas J.; Yoo, Jin-Hyeong; Ott, Ryan T.; Lambert, Paul K.; Petculescu, Gabriela; Simsek, Emrah; Schlagel, Deborah; Lograsso, Thomas A.

    2018-05-01

    Magnetostrictive materials exhibit a strain in the presence of a variable magnetic field. While they normally require large, highly oriented crystallographic grains for high strain values, metal additive manufacturing (3D printing) may be able to produce highly textured polycrystalline rods, with properties comparable to those manufactured using the more demanding free standing zone melting (FSZM) technique. Rods of Co75.8Fe24.2 and Co63.7Fe36.3 have been fabricated using the Laser engineered net shaping (LENSTM) system to evaluate the performance of additively manufactured magnetic and magnetostrictive materials. The 76% Co sample showed an average magnetostriction (λ) of 86 ppm at a stress of 124 MPa; in contrast, the 64% Co sample showed only 27 ppm at the same stress. For direct comparison, a Co67Fe33 single crystal disk, also measured as part of this study, exhibited a magnetostriction value of 131 and 91 microstrain in the [100] and [111] directions, respectively, with a calculated polycrystalline value (λs) of 107 microstrain. Electron back scattered diffraction (EBSD) has been used to qualitatively link the performance with crystallographic orientation and phase information, showing only the BCC phase in the 76% Co sample, but three different phases (BCC, FCC, and HCP) in the 64% Co sample.

  5. Metal-semiconductor transition materials. FeS and VO{sub 2} thin films by RF reactive sputtering

    Energy Technology Data Exchange (ETDEWEB)

    Fu Ganhua

    2007-06-15

    In the present work, two MST systems, FeS and VO{sub 2} thin films were investigated. Iron sulfide thin films over a range of composition were prepared by reactive sputtering. The influence of the substrate, sputter power, substrate temperature and stoichiometry on the structure and MST of iron sulfide films was investigated. Iron sulfide films deposited at different temperatures show temperature dependent structure and MST. FeS films on float glass show (110) and (112) orientations when the substrate temperature is 200 and 500 C, respectively. The transition temperature and width of the hysteresis loop determined from the temperature dependent conductivity curves of iron sulfide films decrease with the substrate temperature. Fe and S excess in FeS films both result in the decrease of the transition temperature and width of the hysteresis loop. The vacuum-annealing affects the MST of FeS films significantly. When FeS films were annealed below the deposition temperature, the transition temperature decreases; otherwise increases. The residual stress plays an important role during the annealing process. The higher the residual stress inside the FeS films is, the higher the transition temperature of FeS films. With the increase of the annealing temperature, the residual stress in FeS films is first released and then enhances, which gives rise first to the decrease and then increase of the transition temperature of FeS films. At high substrate temperatures, the residual stress is higher. In addition, the MST of FeS films was influenced by the ambient aging. With the increase of the aging time, the transition temperature first increases and then decreases. FeS films with different thicknesses were prepared. The correlation between the film thickness (grain size) and the MST switching characteristics of FeS films was established. With the decrease of the grain size, the density of grain boundaries increases, causing the increase of the conductivity of the semiconducting

  6. Metal-semiconductor transition materials. FeS and VO2 thin films by RF reactive sputtering

    International Nuclear Information System (INIS)

    Fu, Ganhua

    2007-06-01

    In the present work, two MST systems, FeS and VO 2 thin films were investigated. Iron sulfide thin films over a range of composition were prepared by reactive sputtering. The influence of the substrate, sputter power, substrate temperature and stoichiometry on the structure and MST of iron sulfide films was investigated. Iron sulfide films deposited at different temperatures show temperature dependent structure and MST. FeS films on float glass show (110) and (112) orientations when the substrate temperature is 200 and 500 C, respectively. The transition temperature and width of the hysteresis loop determined from the temperature dependent conductivity curves of iron sulfide films decrease with the substrate temperature. Fe and S excess in FeS films both result in the decrease of the transition temperature and width of the hysteresis loop. The vacuum-annealing affects the MST of FeS films significantly. When FeS films were annealed below the deposition temperature, the transition temperature decreases; otherwise increases. The residual stress plays an important role during the annealing process. The higher the residual stress inside the FeS films is, the higher the transition temperature of FeS films. With the increase of the annealing temperature, the residual stress in FeS films is first released and then enhances, which gives rise first to the decrease and then increase of the transition temperature of FeS films. At high substrate temperatures, the residual stress is higher. In addition, the MST of FeS films was influenced by the ambient aging. With the increase of the aging time, the transition temperature first increases and then decreases. FeS films with different thicknesses were prepared. The correlation between the film thickness (grain size) and the MST switching characteristics of FeS films was established. With the decrease of the grain size, the density of grain boundaries increases, causing the increase of the conductivity of the semiconducting phase

  7. Manipulating Conduction in Metal Oxide Semiconductors: Mechanism Investigation and Conductance Tuning in Doped Fe2O3 Hematite and Metal/Ga2O3/Metal Heterostructure

    Science.gov (United States)

    Zhao, Bo

    This study aims at understanding the fundamental mechanisms of conduction in several metal oxide semiconductors, namely alpha-Fe2O 3 and beta-Ga2O3, and how it could be tuned to desired values/states to enable a wide range of application. In the first effort, by adding Ti dopant, we successfully turned Fe2O3 from insulating to conductive by fabricated compositionally and structurally well-defined epitaxial alpha-(TixFe1-x)2 O3(0001) films for x ≤ 0.09. All films were grown by oxygen plasma assisted molecular beam epitaxy on Al2O3(0001) sapphire substrate with a buffer layer of Cr2O3 to relax the strain from lattice mismatch. Van der Pauw resistivity and Hall effect measurements reveal carrier concentrations between 1019 and 1020 cm-3 at room temperature and mobilities in the range of 0.1 to 0.6 cm2/V˙s. Such low mobility, unlike conventional band-conduction semiconductor, was attributed to hopping mechanism due to strong electron-phonon interaction in the lattice. More interestingly, conduction mechanism transitions from small-polaron hopping at higher temperatures to variable range hopping at lower temperatures with a transition temperature between 180 to 140 K. Consequently, by adding Ti dopant, conductive Fe 2O3 hematite thin films were achieved with a well-understood conducting mechanism that could guide further device application such as spin transistor and water splitting. In the case of Ga2O3, while having a band gap as high as 5 eV, they are usually conductive for commercially available samples due to unintentional Si doping. However, we discovered the conductance could be repeatedly switched between high resistance state and low resistance state when made into metal/Ga2O3 /metal heterostructure. However, to obtain well controlled switching process with consistent switching voltages and resistances, understanding switching mechanism is the key. In this study, we fabricated resistive switching devices utilizing a Ni/Ga2O3/Ir heterostructure. Bipolar

  8. Experimental determination of the phase equilibria in the Co-Fe-Zr ternary system

    International Nuclear Information System (INIS)

    Wang, C.P.; Yu, Y.; Zhang, H.H.; Hu, H.F.; Liu, X.J.

    2011-01-01

    Research highlights: → We determined four isothermal sections of the Co-Fe-Zr system from 1000 o C to 1300 o C. → No ternary compound was found in the Co-Fe-Zr ternary system. → The solubility of Fe in the liquid phase at 1300 o C is extremely large. → The (Co, Fe) 2 Zr phase form the continuous solution from Co-Zr side to Fe-Zr side. → The solubility of Zr in the fcc (Co, Fe) phase is extremely small. - Abstract: The phase equilibria in the Co-Fe-Zr ternary system were investigated by means of optical microscopy (OM), electron probe microanalysis (EPMA), X-ray diffraction (XRD), and differential scanning calorimetry (DSC) on equilibrated ternary alloys. Four isothermal sections of the Co-Fe-Zr ternary system at 1300 o C, 1200 o C, 1100 o C and 1000 o C were experimentally established. The experimental results indicate that (1) no ternary compound was found in this system; (2) the solubility of Fe in the liquid phase of the Co-rich corner at 1300 o C is extremely large; (3) the liquid phase in the Zr-rich corner and the (Co,Fe) 2 Zr phase form the continuous solid solutions from the Co-Zr side to the Fe-Zr side; (4) the solubility of Zr in the fcc (Co, Fe) phase is extremely small.

  9. A synthetic system links FeFe-hydrogenases to essential E. coli sulfur metabolism

    Directory of Open Access Journals (Sweden)

    Grandl Gerald

    2011-05-01

    Full Text Available Abstract Background FeFe-hydrogenases are the most active class of H2-producing enzymes known in nature and may have important applications in clean H2 energy production. Many potential uses are currently complicated by a crucial weakness: the active sites of all known FeFe-hydrogenases are irreversibly inactivated by O2. Results We have developed a synthetic metabolic pathway in E. coli that links FeFe-hydrogenase activity to the production of the essential amino acid cysteine. Our design includes a complementary host strain whose endogenous redox pool is insulated from the synthetic metabolic pathway. Host viability on a selective medium requires hydrogenase expression, and moderate O2 levels eliminate growth. This pathway forms the basis for a genetic selection for O2 tolerance. Genetically selected hydrogenases did not show improved stability in O2 and in many cases had lost H2 production activity. The isolated mutations cluster significantly on charged surface residues, suggesting the evolution of binding surfaces that may accelerate hydrogenase electron transfer. Conclusions Rational design can optimize a fully heterologous three-component pathway to provide an essential metabolic flux while remaining insulated from the endogenous redox pool. We have developed a number of convenient in vivo assays to aid in the engineering of synthetic H2 metabolism. Our results also indicate a H2-independent redox activity in three different FeFe-hydrogenases, with implications for the future directed evolution of H2-activating catalysts.

  10. Is the enrichment of metals in Mn-Fe nodules from the central Pacific correlated with glacial-interglacial stages?

    Science.gov (United States)

    Wegorzewski, A.; Kuhn, T.

    2012-12-01

    Polymetallic nodules and crusts contain high concentrations of Mn, Fe, Ni, Cu, Co and HFSE. The BGR has been exploring a German license area between the Clarion- and Clipperton Fracture Zone (CCFZ) in the Pacific for nodule abundance and metal content. Nodules are Mn-Fe oxy-hydroxide precipitations consisting of concentrically banded microlayers of different chemical and mineralogical composition. There are layers with high Mn/Fe ratios (3-400) and high Ni+Cu (2-6 wt%) but low Co contents (0.01-0.2 wt%). Mineralogically these layers consists of todorokite and birnessite. In contrast there are layers with low Mn/Fe ≤ 3 and low Ni+Cu (~1 wt%) but increased Co content (0.2-0.5 wt%) and consist mineralogically of Fe-rich vernadite which is epitaxial intergrown with feroxyhyte nanoparticles (Bodei et al., 2007). The different composition of the layers is depending on different growth processes, such as hydrogenetic (metal precipitation from the water column under oxic conditions; Mn/Fe ≤ 3) or diagenetic (metal precipitation from the sediment pore water under oxic (Mn/Fe 3-10) or suboxic (Mn/Fe ≥ 10) conditions; Halbach et al., 1988). X-ray Photoelectron Spectroscopy analyses of recently precipitated outer layers show low Mn/Fe ratios (1.4-2.8). The Ni+Cu content range from 0.34-1.86 wt% and Co shows concentrations between 0.33-1.42 wt%. These results are typical for hydrogenetic processes. They may indicate that in the oxic pore water the same metal enrichment processes prevail as in oxic seawater. Oxygen measurements of near-bottom and pore water proved that the nodules are currently growing under oxic conditions (Mewes, K.,unpub. data). Layers with Mn/Fe ratios of 3-400 cannot grow under such oxic conditions. The high fractionation of Mn and Fe is only possible under suboxic conditions as they are currently predominating in the Peru Basin (PB). Similar growth structures and Mn/Fe ratios of individual layers from CCFZ and PB nodules indicate suboxic conditions

  11. Solid-state phase equilibria in the Fe-Pt-Pr ternary system at 1173 K

    International Nuclear Information System (INIS)

    Ren Jing; Gu Zhengfei; Cheng Gang; Zhou Huaiying

    2005-01-01

    The solid-state phase equilibria in the Fe-Pt-Pr ternary system at 1173 K (Pr ≤ 70%) were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersion spectroscopy (EDS) techniques. The 1173 K isothermal section consists of 13 single-phase regions, 22 two-phase regions and 10 three-phase regions. At 1173 K, we have observed that the maximum solid solubility of Pt in α-Fe is below 1.5 at.% and the solid solution region of Pt in γ-Fe is from 2 to 35 at.%; the maximum solid solubility of Fe in Pt is 18 at.%. The maximum solubility of Fe in PrPt 5 , PrPt 3 , PrPt 2 , Pr 3 Pt 4 , PrPt, Pr 3 Pt 2 and Pr 7 Pt 3 is below 1 at.%. The maximum solubility of Pr in α-(Fe, Pt), γ-(Fe, Pt), FePt, FePt 3 and (Pt, Fe) (the solid solution of Fe in Pt) is 6, 2, 4, 4.5 and 1.5 at.%, respectively. In this work, it is found that the phase Pr 3 Pt 4 does not exist in the ternary system. The binary compounds Fe 7 Pr and Fe 2 Pr and any new ternary compounds were not observed

  12. Review of thermodinamic and mechanical properties of hydrogen-transition metal systems

    International Nuclear Information System (INIS)

    Mathias, H.; Katz, Y.

    1978-04-01

    A large body of fundamental and empirical knowledge has been acquired during many years of research concerning the interactions between hydrogen and metals, the location of hydrogen in metal structures, its mobility in metals and its influence on mechanical properties of metals. Much progress has been made in the understanding of related phenomena, and various theories have been proposed, but considerable disagreement still exist about basic mechanisms involved. The growing interest in these subjects and their important role in science and technology are well documented by many reviews and symposia. A general survey of these topics with reference to experimental results and theories related to thermodynamic and mechanical properties of hydrogen-transition metal systems, such as H-Pd, H-Ti, H-Fe etc. is given in the present review. Special emphasis is given to hydrogen embrittlement of metals

  13. X-ray fluorescence analysis of Fe - Ni - Mo systems

    International Nuclear Information System (INIS)

    Belyaev, E.E.; Ershov, A.V.; Mashin, A.I.; Mashin, N.I.; Rudnevskij, N.K.

    1998-01-01

    Procedures for the X-ray fluorescence determination of the composition and thickness of Fe - Ni - Mo thin films and the concentration of elements in thick films of the Fe - Ni - Mo alloy are developed [ru

  14. Impacts of dust deposition on dissolved trace metal concentrations (Mn, Al and Fe during a mesocosm experiment

    Directory of Open Access Journals (Sweden)

    K. Wuttig

    2013-04-01

    Full Text Available The deposition of atmospheric dust is the primary process supplying trace elements abundant in crustal rocks (e.g. Al, Mn and Fe to the surface ocean. Upon deposition, the residence time in surface waters for each of these elements differs according to their chemical speciation and biological utilization. Presently, however, the chemical and physical processes occurring after atmospheric deposition are poorly constrained, principally because of the difficulty in following natural dust events in situ. In the present work we examined the temporal changes in the biogeochemistry of crustal metals (in particular Al, Mn and Fe after an artificial dust deposition event. The experiment was contained inside trace metal clean mesocosms (0–12.5 m depths deployed in the surface waters of the northwestern Mediterranean, close to the coast of Corsica within the frame of the DUNE project (a DUst experiment in a low Nutrient, low chlorophyll Ecosystem. Two consecutive artificial dust deposition events, each mimicking a wet deposition of 10 g m−2 of dust, were performed during the course of this DUNE-2 experiment. The changes in dissolved manganese (Mn, iron (Fe and aluminum (Al concentrations were followed immediately after the seeding with dust and over the following week. The Mn, Fe and Al inventories and loss or dissolution rates were determined. The evolution of the inventories after the two consecutive additions of dust showed distinct behaviors for dissolved Mn, Al and Fe. Even though the mixing conditions differed from one seeding to the other, Mn and Al showed clear increases directly after both seedings due to dissolution processes. Three days after the dust additions, Al concentrations decreased as a consequence of scavenging on sinking particles. Al appeared to be highly affected by the concentrations of biogenic particles, with an order of magnitude difference in its loss rates related to the increase of biomass after the addition of dust. In

  15. Nano-size metallic oxide particle synthesis in Fe-Cr alloys by ion implantation

    Science.gov (United States)

    Zheng, C.; Gentils, A.; Ribis, J.; Borodin, V. A.; Delauche, L.; Arnal, B.

    2017-10-01

    Oxide Dispersion Strengthened (ODS) steels reinforced with metal oxide nanoparticles are advanced structural materials for nuclear and thermonuclear reactors. The understanding of the mechanisms involved in the precipitation of nano-oxides can help in improving mechanical properties of ODS steels, with a strong impact for their commercialization. A perfect tool to study these mechanisms is ion implantation, where various precipitate synthesis parameters are under control. In the framework of this approach, high-purity Fe-10Cr alloy samples were consecutively implanted with Al and O ions at room temperature and demonstrated a number of unexpected features. For example, oxide particles of a few nm in diameter could be identified in the samples already after ion implantation at room temperature. This is very unusual for ion beam synthesis, which commonly requires post-implantation high-temperature annealing to launch precipitation. The observed particles were composed of aluminium and oxygen, but additionally contained one of the matrix elements (chromium). The crystal structure of aluminium oxide compound corresponds to non-equilibrium cubic γ-Al2O3 phase rather than to more common corundum. The obtained experimental results together with the existing literature data give insight into the physical mechanisms involved in the precipitation of nano-oxides in ODS alloys.

  16. First principles study on spin and orbital magnetism of 3d transition metal monatomic nanowires (Mn, Fe and Co).

    Science.gov (United States)

    Sargolzaei, Mahdi; Samaneh Ataee, S

    2011-03-30

    We have demonstrated the electronic structure and magnetic properties of 3d transition metal nanowires (Mn, Fe and Co) in the framework of relativistic density functional theory. The equilibrium bond lengths were optimized using the generalized gradient approximation. In a full relativistic regime individual spin and orbital moments induced from spin polarization via spin-orbit coupling were calculated. In order to get an upper estimate for orbital moments, we used an orbital polarization correction to our exchange-correlation functional. We found that the orbital magnetic moments of Fe and Co linear chains are strongly enhanced in the presence of an orbital polarization correction. We have calculated the exchange coupling parameters between two nearest-neighbor magnetic atoms according to a Heisenberg-like model in the presence of the orbital polarization correction. We found that the Co and Fe nanowires behave like a ferromagnetic linear chain whereas a Mn monatomic nanowire remains antiferromagnetic. © 2011 IOP Publishing Ltd

  17. Electrical Investigation of Metal-Olivine Systems and Application to the Deep Interior of Mercury

    Science.gov (United States)

    Zhang, Zhou; Pommier, Anne

    2017-12-01

    We report electrical conductivity measurements on metal-olivine systems at about 5 and 6 GPa and up to 1,675°C in order to investigate the electrical properties of core-mantle boundary (CMB) systems. Electrical experiments were conducted in the multianvil apparatus using the impedance spectroscopy technique. The samples are composed of one metal layer (Fe, FeS, FeSi2, or Fe-Ni-S-Si) and one polycrystalline olivine layer, with the metal:olivine ratio ranging from 1:0.7 to 1:9.2. For all samples, we observe that the bulk electrical conductivity increases with temperature from 10-2.5 to 101.8 S/m, which is higher than the conductivity of polycrystalline olivine but lower than the conductivity of the pure metal phase at similar conditions. In some experiments, a conductivity jump is observed at the temperature corresponding to the melting temperature of the metallic phase. Both the metal:olivine ratio and the metal phase geometry control the electrical conductivity of the two-layer samples. By combining electrical results, textural analyses of the samples, and previous studies of the structure and composition of Mercury's interior, we propose an electrical profile of the deep interior of the planet that accounts for a layered CMB-outer core structure. The electrical model agrees with existing conductivity estimates of Mercury's lower mantle and CMB using magnetic observations and thermodynamic calculations, and thus, supports the hypothesis of a layered CMB-outermost core structure in the present-day interior of Mercury. We propose that the layered CMB-outer core structure is possibly electrically insulating, which may influence the planet's structure and cooling history.

  18. [Fe(CN)6]4- decorated mesoporous gelatin thin films for colorimetric detection and as sorbents of heavy metal ions.

    Science.gov (United States)

    Shi, Li; Huang, Hubiao; Sun, Luwei; Lu, Yanping; Du, Binyang; Mao, Yiyin; Li, Junwei; Ye, Zhizhen; Peng, Xinsheng

    2013-09-28

    [Fe(CN)6](4-) decorated mesoporous gelatin films, acting as colorimetric sensors and sorbents for heavy metal ions, were prepared by incorporating [Fe(CN)6](4-) ions into the mesoporous gelatin films through electrostatic interaction. Gelatin-Prussian blue (PB) and gelatin-PB analogue composite films were successfully synthesized by immersing the [Fe(CN)6](4-) decorated gelatin films into aqueous solutions of metal ions, such as Fe(3+), Cu(2+), Co(2+), Pb(2+) and Cd(2+) (all as nitrates). The in situ formation process of PB or its analogues in the films was investigated using quartz crystal microbalance (QCM) measurements. According to the different colors of the PB nanoparticles and its analogues, the [Fe(CN)6](4-) decorated mesoporous gelatin films demonstrated colorimetric sensor abilities for detecting the corresponding metal ions by the naked eye with sufficient sensitivity at 1 ppm level and a quite short response time of 5 minutes. Moreover, due to the [Fe(CN)6](4-) functionality and other functional groups of gelatin itself, this [Fe(CN)6](4-) decorated mesoporous gelatin film shows a tens times higher adsorption ability for heavy metal ions in water than that of activated carbon. Due to both the efficient detection and high adsorption ability for heavy metal ions, this film has wide potential applications for the detection and purification of heavy metal ions from polluted water.

  19. Metal chelator EGCG attenuates Fe(III)-induced conformational transition of α-synuclein and protects AS-PC12 cells against Fe(III)-induced death.

    Science.gov (United States)

    Zhao, Juan; Xu, Lihui; Liang, Qingnan; Sun, Qing; Chen, Congheng; Zhang, Yuan; Ding, Yu; Zhou, Ping

    2017-10-01

    The fibrillation and aggregation of α-synuclein (AS), along with the conformational transition from random coil to β-sheet, are the critical steps in the development of Parkinson's disease (PD). It is acknowledged that iron accumulation in the brain may lead to the fibrillation of AS. However, (-)-epigallocatechin gallate (EGCG) can penetrate the blood-brain barrier, chelate metal ions, and inhibit the fibrillation of amyloid proteins. Therefore, EGCG is warranted to be investigated for its potential to cure amyloid-related diseases. In the present work, we sought to study the effects of EGCG on Fe(III)-induced fibrillation of AS on both molecular and cellular levels. We demonstrate that Fe(III) interacts with the amino residue of Tyr and Ala of AS, then accelerates the fibrillation of AS, and increases intracellular reactive oxygen species (ROS) in the AS transduced-PC12 cells (AS-PC12 cells). However, EGCG significantly inhibits this process by chelating Fe(III) and protects AS-PC12 cells against the toxicity induced by ROS and β-sheet-enriched AS fibrils. These findings yield useful information that EGCG might be a promising drug to prevent and treat the neurodegenerative diseases. © 2017 International Society for Neurochemistry.

  20. A low-spin Fe(III) complex with 100-ps ligand-to-metal charge transfer photoluminescence

    DEFF Research Database (Denmark)

    Chabera, Pavel; Liu, Yizhu; Prakash, Om

    2017-01-01

    sufficiently to realize a long charge-transfer lifetime of 100 picoseconds (ps) and room-temperature photoluminescence. This species is a low-spin Fe(III) d(5) complex, and emission occurs from a long-lived doublet ligand-to-metal charge-transfer ((LMCT)-L-2) state that is rarely seen for transition-metal...... complexes(4,16,17). The absence of intersystem crossing, which often gives rise to large excited-state energy losses in transition-metal complexes, enables the observation of spin-allowed emission directly to the ground state and could be exploited as an increased driving force in photochemical reactions......Transition-metal complexes are used as photosensitizers(1), in light-emitting diodes, for biosensing and in photocatalysis(2). A key feature in these applications is excitation from the ground state to a charge-transfer state(3,4); the long charge-transfer-state lifetimes typical for complexes...

  1. Kinetic Study of Crystallization Process in Fe32Ni36Cr14P12B6 Metallic Glass

    International Nuclear Information System (INIS)

    Lad, Kirit; Pratap, Arun; Rao, T. L. Shanker

    2010-01-01

    Kinetics of crystallization process in a Fe-based metallic glass 2826A (Fe 32 Ni 36 Cr 14 P 12 B 6 ) has been studied with the help of differential scanning calorimetry(DSC). It is found that the 2826A metallic glass exhibits two overlapping crystallization peaks. The activation energy for crystallization (E) and the Avrami exponent (n) for the two crystallization peaks have been obtained using the Kolmogorov-Jhonson-Mehl-Avrami (KJMA) equation. The so-obtained values of E and n have been utilized to derive normalized heat flow curves. It has been observed that the theoretical heat flow curves obtained using KJMA equation show large deviations from the experimental curves for the first peak whereas the curves are in very close agreement for the second peak. This suggests that kinetics of crystallization process during the first peak cannot be described correctly in KJMA formalism.

  2. Kinetic Study of Crystallization Process in Fe32Ni36Cr14P12B6 Metallic Glass

    Science.gov (United States)

    Lad, Kirit; Rao, T. L. Shanker; Pratap, Arun

    2010-06-01

    Kinetics of crystallization process in a Fe-based metallic glass 2826A (Fe32Ni36Cr14P12B6) has been studied with the help of differential scanning calorimetry(DSC). It is found that the 2826A metallic glass exhibits two overlapping crystallization peaks. The activation energy for crystallization (E) and the Avrami exponent (n) for the two crystallization peaks have been obtained using the Kolmogorov-Jhonson-Mehl-Avrami (KJMA) equation. The so-obtained values of E and n have been utilized to derive normalized heat flow curves. It has been observed that the theoretical heat flow curves obtained using KJMA equation show large deviations from the experimental curves for the first peak whereas the curves are in very close agreement for the second peak. This suggests that kinetics of crystallization process during the first peak cannot be described correctly in KJMA formalism.

  3. Temperature Dependent Magnetic Anisotropy in Metallic Magnets from an Ab Initio Electronic Structure Theory: L10-Ordered FePt

    Science.gov (United States)

    Staunton, J. B.; Ostanin, S.; Razee, S. S.; Gyorffy, B. L.; Szunyogh, L.; Ginatempo, B.; Bruno, Ezio

    2004-12-01

    Using a first-principles, relativistic electronic structure theory of finite temperature metallic magnetism, we investigate the variation of magnetic anisotropy K with magnetization M in metallic ferromagnets. We apply the theory to the high uniaxial K material, L10-ordered FePt, and find its magnetic easy axis perpendicular to the Fe/Pt layers for all M and K to be proportional to M2 for a broad range of values of M. For small M, near the Curie temperature, the calculations pick out the easy axis for the onset of magnetic order. Our abinitio results for this important magnetic material agree well with recent experimental measurements, whereas the single-ion anisotropy model fails to give the correct qualitative behavior.

  4. Microstructure and High Temperature Mechanical Property of Fe-Cr-B Based Metal/Ceramic Composite Manufactured by Metal Injection Molding Process

    Science.gov (United States)

    Lee, Kee-Ahn; Gwon, Jin-Han; Yoon, Tae-Sik

    2018-02-01

    This study investigated the microstructure and the room and high temperature mechanical properties of Fe-Cr-B alloy manufactured by metal injection molding. In addition, hot isostatic pressing was performed to increase the density of the material, and a comparison of properties was made. Microstructural observation confirmed a bi-continuous structure composed of a three-dimensional network of α-Fe phase and (Cr,Fe)2B phase. The HIPed specimen featured a well-formed adhesion between the α-Fe phase and boride, and the number of fine pores was significantly reduced. The tensile results confirmed that the HIPed specimen (RT to 900 °C) had higher strengths compared to the as-sintered specimen, and the change of elongation starting from 700 °C was significantly greater in the HIPed specimen. Fractography suggested that cracks propagated mostly along the interface between the α-Fe matrix and boride in the as-sintered specimen, while direct fracture of boride was observed in addition to interface separation in the HIPed specimen.

  5. Microstructure and High Temperature Mechanical Property of Fe-Cr-B Based Metal/Ceramic Composite Manufactured by Metal Injection Molding Process

    Science.gov (United States)

    Lee, Kee-Ahn; Gwon, Jin-Han; Yoon, Tae-Sik

    2018-03-01

    This study investigated the microstructure and the room and high temperature mechanical properties of Fe-Cr-B alloy manufactured by metal injection molding. In addition, hot isostatic pressing was performed to increase the density of the material, and a comparison of properties was made. Microstructural observation confirmed a bi-continuous structure composed of a three-dimensional network of α-Fe phase and (Cr,Fe)2B phase. The HIPed specimen featured a well-formed adhesion between the α-Fe phase and boride, and the number of fine pores was significantly reduced. The tensile results confirmed that the HIPed specimen (RT to 900 °C) had higher strengths compared to the as-sintered specimen, and the change of elongation starting from 700 °C was significantly greater in the HIPed specimen. Fractography suggested that cracks propagated mostly along the interface between the α-Fe matrix and boride in the as-sintered specimen, while direct fracture of boride was observed in addition to interface separation in the HIPed specimen.

  6. Insights into magnetic interactions in a monodisperse Gd{sub 12}Fe{sub 14} metal cluster

    Energy Technology Data Exchange (ETDEWEB)

    Zheng, Xiu-Ying; Zhang, Hui; Liu, Pengxin; Du, Ming-Hao; Han, Ying-Zi; Wei, Rong-Jia; Kong, Xiang-Jian; Long, La-Sheng; Zheng, Lan-Sun [Collaborative Innovation Center of Chemistry for Energy Materials, State Key Lab. of Physical Chemistry of Solid Surface and Dept. of Chemistry, College of Chemistry and Chemical Engineering, Xiamen Univ. (China); Wang, Zhenxing; Ouyang, Zhong-Wen [Wuhan National High Magnetic Field Center and School of Physics, Huazhong University of Science and Technology, Wuhan (China); Zhuang, Gui-Lin [College of Chemcal Engineering, Zhejiang University of Technology, Hangzhou (China)

    2017-09-11

    The largest Ln-Fe metal cluster [Gd{sub 12}Fe{sub 14}(μ{sub 3}-OH){sub 12}(μ{sub 4}-OH){sub 6}(μ{sub 4}-O){sub 12}(TEOA){sub 6}(CH{sub 3}COO){sub 16}(H{sub 2} O){sub 8}].(CH{sub 3}COO){sub 2}(CH{sub 3}CN){sub 2}.(H{sub 2}O){sub 20} (1) and the core-shell monodisperse metal cluster of 1 a rate at SiO{sub 2} (1 a=[Gd{sub 12}Fe{sub 14}(μ{sub 3}-OH){sub 12}(μ{sub 4}-OH){sub 6}(μ{sub 4}-O){sub 12}(TEOA){sub 6}(CH{sub 3}COO){sub 16} (H{sub 2}O){sub 8}]{sup 2+}) were prepared. Experimental and theoretical studies on the magnetic properties of 1 and 1 a rate at SiO{sub 2} reveal that encapsulation of one cluster into one silica nanosphere not only effectively decreases intermolecular magnetic interactions but also significantly increases the zero-field splitting effect of the outer layer Fe{sup 3+} ions. (copyright 2017 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

  7. Fe-N-C electrocatalysts for oxygen reduction reaction synthesized by using aniline salt and Fe3+/H2O2 catalytic system

    KAUST Repository

    Bukola, Saheed

    2014-11-01

    Non-precious metal (NPM) catalysts are synthesized by polymerizing aniline salt using an aqueous Fe3+/H2O2 coupled catalytic system on a carbon matrix with a porous creating agent. The sulfur containing compunds such as ammonium peroxydisulfate, are eliminated in this method resulting in a much simpler process. The catalysts\\' porous structures are enhanced with ammonium carbonate as a sacrificial material that yields voids when decomposed during the heat treatment at 900 °C in N2 atmosphere. Two catalysts Fe-N-C/Vu and Fe-N-C/KB (Vu = Vulcan and KB = Ketjen black) were synthesized and characterized. Their oxygen reduction reaction (ORR) activities were investigated using a rotating ring-disk electrode (RRDE) in both 0.1 M KOH and 0.1 M HClO4. The catalysts show improved ORR activities close to that of Pt-based catalysts, low H2O2 formation and also demonstrated a remarkable tolerance towards methanol oxidation.

  8. Micromagnetic finite element study for magnetic properties of nanocomposite exchange coupled Nd{sub 2}Fe{sub 14}B/α-Fe multilayer systems

    Energy Technology Data Exchange (ETDEWEB)

    Ryo, Hyok-Su [School of Material Science and Engineering, Harbin Institute of Technology, Harbin 150001 (China); Faculty of Physics, Kim Il Sung University, Pyongyang 999093, Democratic People’s Republic of Korea (Korea, Republic of); Hu, Lian-Xi [School of Material Science and Engineering, Harbin Institute of Technology, Harbin 150001 (China); Kim, Jin-Guk [School of Material Science and Engineering, Harbin Institute of Technology, Harbin 150001 (China); Faculty of Physics, Kim Il Sung University, Pyongyang 999093, Democratic People’s Republic of Korea (Korea, Republic of); Yang, Yu-Lin [School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin 150001 (China)

    2017-03-15

    In this study, magnetic properties of exchange coupled nanocomposite multilayer thin films constructed alternately with magnetic hard Nd{sub 2}Fe{sub 14}B layers and soft α-Fe layers have been studied by micromagnetic finite element method (FEM). According to the results, effects of the thicknesses of layers and the magneto-crystalline anisotropy on the magnetic properties of the Nd{sub 2}Fe{sub 14}B/α-Fe multilayer systems have been estimated. On the other hand, the results have been analyzed by means of efficiency of interphase exchange coupling, which can be estimated by volume ratios of exchange coupled areas between magnetically hard Nd{sub 2}Fe{sub 14}B and soft α-Fe phase layers. The results show that the magnetic properties of exchange coupled Nd{sub 2}Fe{sub 14}B/α-Fe multilayer systems can be enhanced by efficient interphase exchange coupling between magnetically hard Nd{sub 2}Fe{sub 14}B layers and soft α-Fe layers. - Highlights: • Phase layer thicknesses dependence of magnetic properties of Nd{sub 2}Fe{sub 14}B/α-Fe multilayers. • Analyzation of the effectiveness of exchange coupling between the Nd{sub 2}Fe{sub 14}B and α-Fe layers. • Dependence of the magnetic properties on direction of external field of exchange coupled Nd{sub 2}Fe{sub 14}B/α-Fe multilayers. • Dependence of the magnetic properties on magneto-crystalline anisotropy of exchange coupled Nd{sub 2}Fe{sub 14}B/α-Fe multilayers.

  9. Thermal annealing behavior of nano-size metal-oxide particles synthesized by ion implantation in Fe-Cr alloy

    Science.gov (United States)

    Zheng, C.; Gentils, A.; Ribis, J.; Borodin, V. A.; Descoins, M.; Mangelinck, D.; Dalle, F.; Arnal, B.; Delauche, L.

    2017-05-01

    Oxide dispersion strengthened (ODS) steels are promising structural materials for the next generation nuclear reactors, as well as fusion facilities. The detailed understanding of the mechanisms involved in the precipitation of nano-oxides during ODS steel production would strongly contribute to the improvement of the mechanical properties and the optimization of manufacturing of ODS steels, with a potentially strong economic impact for their industrialization. A useful tool for the experimental study of nano-oxide precipitation is ion implantation, a technique that is widely used to synthesize precipitate nanostructures in well-controlled conditions. Earlier, we have demonstrated the feasibility of synthesizing aluminum-oxide particles in the high purity Fe-10Cr alloy by consecutive implantation with Al and O ions at room temperature. This paper describes the effects of high-temperature annealing after the ion implantation stage on the development of the aluminum based oxide nanoparticle system. Using transmission electron microscopy and atom probe tomography experiments, we demonstrate that post-implantation heat treatment induces the growth of the nano-sized oxides in the implanted region and nucleation of new oxide precipitates behind the implantation zone as a result of the diffusion driven broadening of implant profiles. A tentative scenario for the development of metal-oxide nano-particles at both ion implantation and heat treatment stages is suggested based on the experimental observations.

  10. Linguistic Documentation of Metal System

    Science.gov (United States)

    1978-05-01

    art beyond its current limitations, and the Report documents an important milestone in machine translation KtD. The System is based on cumulative...ARITHmetic B MATHematics ARTS , fine ASTRonomy « same ASTROLogy « ASTRology ATHLetics BACTeriology « MEDical BAKing BIBlical « BIBLical...Ecclesiastical = RELIGion ’ ECONomics * same ELectricity ■ ELECTRicity EMBRoidery ENGINeering = TECHnology ENGRaving ENTOMology = ZOOlogy [ENTomology

  11. Composition design of Ti–Cr–Mn–Fe alloys for hybrid high-pressure metal hydride tanks

    Energy Technology Data Exchange (ETDEWEB)

    Cao, Zhijie [School of Materials Science and Engineering, Key Laboratory of Advanced Energy Storage Materials of Guangdong Province, South China University of Technology, Guangzhou 510641 (China); China-Australia Joint Laboratory for Energy & Environmental Materials, South China University of Technology, Guangzhou 510641 (China); Ouyang, Liuzhang, E-mail: meouyang@scut.edu.cn [School of Materials Science and Engineering, Key Laboratory of Advanced Energy Storage Materials of Guangdong Province, South China University of Technology, Guangzhou 510641 (China); China-Australia Joint Laboratory for Energy & Environmental Materials, South China University of Technology, Guangzhou 510641 (China); Key Laboratory for Fuel Cell Technology in Guangdong Province, Guangzhou 510641 (China); Wang, Hui; Liu, Jiangwen [School of Materials Science and Engineering, Key Laboratory of Advanced Energy Storage Materials of Guangdong Province, South China University of Technology, Guangzhou 510641 (China); China-Australia Joint Laboratory for Energy & Environmental Materials, South China University of Technology, Guangzhou 510641 (China); Sun, Lixian [Guangxi Collaborative Innovation Center of Structure and Property for New Energy and Materials, Guilin 541004 (China); Zhu, Min, E-mail: memzhu@scut.edu.cn [School of Materials Science and Engineering, Key Laboratory of Advanced Energy Storage Materials of Guangdong Province, South China University of Technology, Guangzhou 510641 (China); China-Australia Joint Laboratory for Energy & Environmental Materials, South China University of Technology, Guangzhou 510641 (China)

    2015-08-05

    Highlights: • New non-stoichiometric Ti–Cr–Mn–Fe alloys are prepared for the hybrid tank. • (Ti{sub 0.85}Zr{sub 0.15}){sub 1.1}Cr{sub 0.925}MnFe{sub 0.075} has the best overall properties. • The desorption pressure at 0 °C is 10.6 atm. • The reversible gravimetric density remains as a high value of 1.49 wt%. - Abstract: (Ti{sub 0.85}Zr{sub 0.15}){sub 1.1}Cr{sub 1−x}MnFe{sub x} (x = 0, 0.05, 0.075, 0.1, 0.15) alloys with a C14-type Laves structure have been investigated for potential application in hybrid high-pressure metal hydride tanks used for fuel cell vehicles. The effects of the partial substitution of Cr with Fe on the hydrogen storage properties of (Ti{sub 0.85}Zr{sub 0.15}){sub 1.1}CrMn have been systematically investigated. Results show that the desorption plateau pressure increases with increasing the Fe content in (Ti{sub 0.85}Zr{sub 0.15}){sub 1.1}Cr{sub 1−x}MnFe{sub x} alloys, whereas the hydrogen capacity decreases. Among these alloys, (Ti{sub 0.85}Zr{sub 0.15}){sub 1.1}Cr{sub 0.925}MnFe{sub 0.075} has the best overall properties, with a hydrogen desorption pressure of 10.6 atm and a reversible capacity of 1.54 wt% at 0 °C under the pressure range between 0.1 atm and 120 atm.

  12. In situ formed Fe-N doped metal organic framework@carbon nanotubes/graphene hybrids for a rechargeable Zn-air battery.

    Science.gov (United States)

    Yang, Wenxiu; Zhang, Yelong; Liu, Xiangjian; Chen, Lulu; Jia, Jianbo

    2017-11-30

    This study presents an in situ route to produce 3D Fe-N doped metal organic framework@carbon nanotubes/graphene (Fe-MOF@CNTs-G) hybrids as efficient oxygen reduction reaction (ORR) catalysts in both basic and acidic solutions. A rechargeable zinc-air battery assembled with Fe-MOF@CNTs-G exhibits a lower charge/discharge overpotential than the commercial IrO 2 + 20% Pt/C catalyst.

  13. Assessment of metal bioavailability in the vineyard soil-grapevine system using different extraction methods.

    Science.gov (United States)

    Vázquez Vázquez, Francisco A; Pérez Cid, Benita; Río Segade, Susana

    2016-10-01

    This study was focused on the assessment of single and sequential extraction methods to predict the bioavailability of metals in the vineyard soil-grapevine system. The modified BCR sequential extraction method and two single-step extraction methods based on the use of EDTA and acetic acid were applied to differently amended vineyard soils. The variety effect was studied on the uptake of metals by leaves and grapes. Most of the elements studied (Ca, Mg, Cu, Fe, Mn, Zn and Pb) were weakly mobilized from vineyard soils, with the exception of Cu and Mn. The determination of total metal content in leaves and grapes showed a different accumulation pattern in the two parts of the vine. A significant relationship was observed, for all the elements studied except for Fe, between the content bioavailable in the soil and the accumulated in both leaves and grapes (R=0.602-0.775, p<0.01). Copyright © 2016 Elsevier Ltd. All rights reserved.

  14. A metal-organic framework-templated synthesis of γ-Fe2O3 nanoparticles encapsulated in porous carbon for efficient and chemoselective hydrogenation of nitro compounds.

    Science.gov (United States)

    Li, Yang; Zhou, Yu-Xiao; Ma, Xiao; Jiang, Hai-Long

    2016-03-18

    The γ-Fe2O3 nanoparticles well dispersed in porous carbon were fabricated via a Fe-based metal-organic framework-templated pyrolysis. The resultant product exhibits excellent catalytic activity, chemoselectivity and magnetic recyclability for the hydrogenation of diverse nitro compounds under mild conditions.

  15. Assessment of the Binding of Protons, Al and Fe to Biochar at Different pH Values and Soluble Metal Concentrations

    Directory of Open Access Journals (Sweden)

    Tan Dang

    2018-01-01

    Full Text Available Biochar can retain large amounts of protons and metals in the drainage water from acid sulfate soils and mine sites. Metal sorption can, however, be influenced by many factors, such as pH and metal composition. This study investigated proton, Al, and Fe retention capacity of eucalyptus biochar (1% w/v at different pH and metal concentrations. In the absence of metals, the biochar had a high proton binding capacity, (up to 0.035 mmol of H+, whereas its capacity to retain hydroxide ions was limited. A batch experiment was carried out at pH 4 and pH 7 with 10−6, 10−5, 10−4, 10−3, and 10−2 M of added Fe or Al. Added metals precipitated considerably prior to addition of the biochar except that Al remained highly soluble at pH 4. The biochar had a high retention capacity for Al and Fe; at high (>1 mM concentrations, over 80% of soluble metals were retained. Metal competition for binding sites of both Al and Fe at different ratios was investigated, but increasing concentrations of one metal did not reduce retention of the other. The results confirmed that biochar has high metal binding capacity under both acidic and neutral conditions.

  16. Phase relationships of the system Fe-Ni-S and structure of the high-pressure phase of (Fe1-xNix)3S2

    Science.gov (United States)

    Urakawa, Satoru; Kamuro, Ryota; Suzuki, Akio; Kikegawa, Takumi

    2018-04-01

    The phase relationships of the Fe-Ni-S system at 15 GPa were studied by high pressure quench experiments. The stability fields of (Fe,Ni)3S and (Fe,Ni)3S2 and the melting relationships of the Fe-Ni-S system were determined as a function of Ni content. The (Fe,Ni)3S solid solution is stable in the composition of Ni/(Fe + Ni) > 0.7 and melts incongruently into an Fe-Ni alloy + liquid. The (Fe,Ni)3S2 makes a complete solid solution and melts incongruently into (Fe,Ni)S + liquid, whose structure was determined to show Cmcm-orthorhombic symmetry by in situ synchrotron X-ray diffraction experiments. The eutectic contains about 30 at.% of S, and its temperature decreases with increasing Ni content with a rate of ∼5 K/at.% from 1175 K. The density of the Fe-FeS eutectic composition (Fe70S30) liquid is evaluated to be 6.93 ± 0.08 g/cm3 at 15 GPa and 1200 K based on the Clausius-Clapeyron relations and densities of subsolidus phases. The Fe-Ni-S liquids are a primary sulfur-bearing phase in the deep mantle with a reducing condition (250-660 km depth), and they would play a significant role in the carbon cycle as a carbon host as well as in the generation of diamond.

  17. Metal (Co, Fe) tribenzotetraazachlorin-fullerene conjugates: impact of direct p-bonding on the redox behaviour and oxygen reduction reaction

    CSIR Research Space (South Africa)

    Ozoemena, KI

    2009-06-01

    Full Text Available on the solution electrochemistry of these metallophthalocyanine (MPc)complexes. The more electron-withdrawing C60 substituent suppressed ORR compared to the –SO2Bu Metal (Co, Fe) tribenzotetraazachlorin–fulleren p-bonding on the redox behaviour and oxyge...., Metal (Co, Fe) tribenzotetraa behaviour and oxygen reduction reaction, Electrochem. Commun. (2009), doi:1 zachlorin–fullerene conjugates: Impact of direct p-bonding on the redox 0.1016/j.elecom.2009.04.011 ...

  18. Co-adsorption and sequential adsorption of the co-existence four heavy metal ions and three fluoroquinolones on the functionalized ferromagnetic 3D NiFe2O4porous hollow microsphere.

    Science.gov (United States)

    Liu, Xueyan; Liu, Mingyang; Zhang, Lei

    2018-02-01

    Functionalized magnetic microsphere NiFe 2 O 4 (MS-NiFe 2 O 4 ) with a 3D hierarchical porous hollow structure was fabricated using urea as the modifier and soft templates by a simple one-pot solvothermal method. The constructed MS-NiFe 2 O 4 shows excellent dual functions which can not only undergo simultaneous rapid removal of the co-existence metal ions (Cu 2+ , Cd 2+ , Cr 3+ and Zn 2+ ions), but also availably adsorb fluoroquinolone (FQs) (ciprofloxacin (CIP), enrofloxacin (ENR) and norfloxacin (NOR)), and is easily recycled using an external magnetic field. The removal efficiency of eight targets could all reach up to 80% within 60min at pH 5. The independent adsorption of single contaminants, the competitive adsorption of multiple heavy metal ions/organic contaminants, the simultaneous and sequential adsorption of the co-existence of inorganic and organic contaminants onto MS-NiFe 2 O 4 were explored in detail. Competition adsorption occurred between the same type of contaminants. For different types of contaminants, four metal ions did not affect the adsorption of the other three FQs in the sequential and simultaneously adsorption system, and vice versa. The possible adsorption mechanism between targets and MS-NiFe 2 O 4 was revealed. Copyright © 2017. Published by Elsevier Inc.

  19. Phase equilibrium of the system Ag-Fe-Nd, and Nd extraction from magnet scraps using molten silver

    International Nuclear Information System (INIS)

    Takeda, O.; Okabe, T.H.; Umetsu, Y.

    2004-01-01

    To develop a new recycling process, we examined the direct extraction of neodymium (Nd) metal from Nd-Fe-B magnet scraps using molten silver (Ag) as an extraction medium. Prior to the extraction experiment, the phase equilibrium of the system Ag-Fe-Nd was investigated to estimate the theoretical extraction limit. It was observed that the Fe/Nd 2 Fe 17 mixture equilibrates with the molten Ag-Nd alloy containing 50-52 mol% Nd (57-59 mass% Nd) at 1363 K. The experimental results were in good agreement with the thermodynamic calculation based on literature values. By reacting Nd-Fe-B magnet scraps with molten silver at 1273 K, more than 90% of the neodymium in the scrap was extracted, and an Ag-Nd alloy containing 40-50 mass% Nd was obtained. The neodymium in the Ag-Nd alloy was separated from silver as Nd 2 O 3 by oxidizing the obtained alloy in air. Although the wettability of Nd 2 O 3 with molten silver caused some difficulties in the separation of neodymium from silver, molten silver is shown to be an effective medium for neodymium extraction from magnet scrap

  20. Isothermal section of the Er-Fe-Al ternary system at 800 oC

    International Nuclear Information System (INIS)

    Jemmali, M.; Walha, S.; Pasturel, M.; Tougait, O.; Ben Hassen, R.; Noel, H.

    2010-01-01

    Physico-chemical analysis techniques, including X-ray diffraction and Scanning Electron Microscope-Energy Dispersive X-ray Spectroscopy, were employed to construct the isothermal section of the Er-Fe-Al system at 800 o C. At this temperature, the phase diagram is characterized by the formation of five intermediate phases, ErFe 12-x Al x with 5 ≤ x ≤ 8 (ThMn 12 -type), ErFe 1+x Al 1-x with -0.2 ≤ x ≤ 0.75 (MgZn 2 -type), ErFe 3-x Al x with 0.5 2 Al-type), Er 2 Fe 17-x Al x with 4.74 ≤ x ≤ 5.7 (TbCu 7 -type) and Er 2 Fe 17-x Al x with 5.7 2 Zn 17 -type), seven extensions of binaries into the ternary system; ErFe x Al 3-x with x 3 Cu-type), ErFe x Al 2-x with x ≤ 0.68 (MgCu 2 -type), Er 2 Fe x Al 1-x with x ≤ 0.25 (Co 2 Si-type), ErFe 2-x Al x with x ≤ 0.5 (MgCu 2 -type), ErFe 3-x Al x with x ≤ 0.5 (Be 3 Nb-type), Er 6 Fe 23-x Al x with x ≤ 8 (Th 6 Mn 23 -type), and Er 2 Fe 17-x Al x with x ≤ 4.75 (Th 2 Ni 17 -type) and one intermetallic compound; the ErFe 2 Al 10 (YbFe 2 Al 10 -type).

  1. Hierarchically structured manganese oxide-coated magnetic nanocomposites for the efficient removal of heavy metal ions from aqueous systems.

    Science.gov (United States)

    Kim, Eun-Ju; Lee, Chung-Seop; Chang, Yoon-Young; Chang, Yoon-Seok

    2013-10-09

    In this study, hierarchical MnO2-coated magnetic nanocomposite (Fe3O4/MnO2) was synthesized by a mild hydrothermal process, and its application for removing heavy metal ions from contaminated water systems was examined. Structural characterization showed that the Fe3O4 nanoparticle core was coated with amorphous MnO2 shell with flowerlike morphology. The as-prepared nanocomposite had a large surface area and high magnetic saturation value, which ensured its good sorption ability and convenience of separation. Fe3O4/MnO2 exhibited a greatly improved removal capacity toward four different heavy metals (Cd(II), Cu(II), Pb(II), and Zn(II)) compared to unmodified Fe3O4 nanoparticles. The adsorption property of Fe3O4/MnO2 was studied with Cd(II) in more detail. The sorption equilibrium data were well fitted to the Langmuir model, and the maximum adsorption capacity toward Cd(II) was 53.2 mg g(-1). Fe3O4/MnO2 retained over 80% of its adsorption capacity under various solution conditions that are typically encountered in natural waters. This nanocomposite was easily recovered and reused through consecutive adsorption-desorption experiments with the assistance of an external magnetic field. Overall, the findings propose that Fe3O4/MnO2 could be used as an effective recyclable adsorbent for heavy metal ions.

  2. Effects of metal ions on growth, β-oxidation system, and thioesterase activity of Lactococcus lactis.

    Science.gov (United States)

    Li, Liang; Ma, Ying

    2014-10-01

    The effects of divalent metal ions (Ca(2+), Mg(2+), Fe(2+), and Cu(2+)) on the growth, β-oxidation system, and thioesterase activity of Lactococcus lactis were investigated. Different metal ions significantly influenced the growth of L. lactis: Ca(2+) and Fe(2+) accelerated growth, whereas Cu(2+) inhibited growth. Furthermore, Mg(2+) inhibited growth of L. lactis at a low concentration but stimulated growth of L. lactis at a high concentration. The divalent metal ions had significant effects on activity of the 4 key enzymes of the β-oxidation system (acyl-CoA dehydrogenase, enoyl-CoA hydratase, L-3-hydroxyacyl-CoA dehydrogenase, and thiolase) and thioesterase of L. lactis. The activity of acyl-CoA dehydrogenases increased markedly in the presence of Ca(2+) and Mg(2+), whereas it decreased with 1 mmol/L Fe(2+) or 12 mmol/L Mg(2+). All the metal ions could induce activity of enoyl-CoA hydratase. In addition, 12 mmol/L Mg(2+) significantly stimulated activity of L-3-hydroxyacyl-CoA dehydrogenase, and all metal ions could induce activity of thiolase, although thiolase activity decreased significantly when 0.05 mmol/L Cu(2+) was added into M17 broth. Inhibition of thioesterase activity by all 4 metal ions could be reversed by 2 mmol/L Ca(2+). These results help us understand the effect of metal ions on the β-oxidation system and thioesterase activity of Lactococcus lactis. Copyright © 2014 American Dairy Science Association. Published by Elsevier Inc. All rights reserved.

  3. Experiments on Lunar Core Composition: Phase Equilibrium Analysis of A Multi-Element (Fe-Ni-S-C) System

    Science.gov (United States)

    Go, B. M.; Righter, K.; Danielson, L.; Pando, K.

    2015-01-01

    Previous geochemical and geophysical experiments have proposed the presence of a small, metallic lunar core, but its composition is still being investigated. Knowledge of core composition can have a significant effect on understanding the thermal history of the Moon, the conditions surrounding the liquid-solid or liquid-liquid field, and siderophile element partitioning between mantle and core. However, experiments on complex bulk core compositions are very limited. One limitation comes from numerous studies that have only considered two or three element systems such as Fe-S or Fe-C, which do not supply a comprehensive understanding for complex systems such as Fe-Ni-S-Si-C. Recent geophysical data suggests the presence of up to 6% lighter elements. Reassessments of Apollo seismological analyses and samples have also shown the need to acquire more data for a broader range of pressures, temperatures, and compositions. This study considers a complex multi-element system (Fe-Ni-S-C) for a relevant pressure and temperature range to the Moon's core conditions.

  4. STRUCTURE OF Co(III) AND Fe(III) TRANSITION METAL IONS IN ...

    African Journals Online (AJOL)

    Bulletin of the Chemical Society of Ethiopia ... The hydration structures of Co(III) and Fe(III) ions have been investigated by Metropolis Monte Carlo (MC) simulations using only ion-water pair interaction ... KEY WORDS: Metropolis Monte Carlo simulation, Hydration structure, Fe(III) and Co(III) ions, Three-body corrections

  5. Separation of rare earths and other valuable metals from deep-eutectic solvents: a new alternative for the recycling of used NdFeB magnets

    OpenAIRE

    Riano, Sofia; Petranikova, Martina; Onghena, Bieke; Vander Hoogerstraete, Tom; Banerjee, Dipanjan; Foreman, Mark R. St J.; ekberg, christian; BINNEMANS, Koen

    2017-01-01

    International audience; Deep-eutectic solvents (DESs) are used as a promising alternative to aqueous solutions for the recovery of valuable metals from NdFeB magnets. A deep-eutectic solvent based on choline chloride and lactic acid (molar ratio 1 : 2) was used for the leaching of rare earths and other metals from NdFeB magnets. A process for the separation of Fe, B and Co from Nd and Dy in the deep-eutectic solvent was developed by using the ionic liquid tricaprylmethylammonium thiocyanate (...

  6. Effect of particle size and alloying with different metals on {sup 57}Fe Moessbauer spectra

    Energy Technology Data Exchange (ETDEWEB)

    Nazir, Rabia; Mazhar, Muhammad, E-mail: mazhar42pk@yahoo.com [Quaid-i-Azam University, Department of Chemistry (Pakistan); Siddique, Muhammad [PINSTECH, Physics Division (Pakistan); Hussain, S. Tajammul [Quaid-i-Azam University, Department of Chemistry (Pakistan)

    2009-02-15

    Iron nanoparticles of various sizes have been synthesized using the chemical route which involves the preparation of iron bipyridine complexes in presence of different capping agents followed by thermal decomposition at 450 deg. C in inert atmosphere. The bimetallic nanoalloys of Fe with Mg and Pd have also been prepared by following the same route. The resulting nanoparticles have been characterized by EDX-RF, XRD, AFM and {sup 57}Fe Moessbauer spectroscopy. The appearance of quadrupole doublets in the Moessbauer spectra of Fe nanoparticles indicates the absence of magnetic interaction and variation in parameters is due to the varying particle size. The Moessbauer spectrum of Fe-Mg{sub 2} bimetallic nanoalloy shows two doublets indicating the presence of superparamagnetism. The two doublets can be attributed to change in s-electron density of iron resulting from its two neighboring magnesium atoms. Fe-Pd nanoalloy Moessbauer spectrum is characterized by having a superparamagnetic doublet and a ferromagnetic sextet.

  7. The role of metal-support interaction for CO-free hydrogen from low temperature ethanol steam reforming on Rh-Fe catalysts.

    Science.gov (United States)

    Choong, Catherine K S; Chen, Luwei; Du, Yonghua; Schreyer, Martin; Daniel Ong, S W; Poh, Chee Kok; Hong, Liang; Borgna, Armando

    2017-02-08

    Rh-Fe catalysts supported on Ca-Al 2 O 3 , MgO and ZrO 2 were evaluated in ethanol steam reforming at 623 K and compared to Rh catalysts on the same supports without iron promotion. The metal-support interaction among the three entities, i.e. Rh ↔ Fe 2 O 3 ← support (ZrO 2 , MgO and Ca-Al 2 O 3 ) was investigated using H 2 -chemisorption, TEM, XPS and in situ techniques such as DRIFTS, temperature-resolved XRD and XAS. As compared to the unpromoted Rh catalysts on the same supports, the CO selectivity is depressed in the presence of iron on Rh/MgO and Rh/Ca-Al 2 O 3 , the latter being significantly superior. The role of metal-support interaction for CO-free hydrogen generation was unravelled using a combination of techniques. It was found that the reducibility of iron oxide determines the extent of the strong metal support interaction between Rh and Fe 2 O 3 and the reducibility of iron oxide was affected by the support. On Rh-Fe/Ca-Al 2 O 3 , a good balance of the interaction between Rh, Fe 2 O 3 and Ca-Al 2 O 3 prevents strong metal support interaction between Rh and Fe 2 O 3 and thus promotes CO elimination via water-gas-shift reaction on Rh-Fe x O y sites.

  8. Coupling catalytic hydrolysis and oxidation of HCN over HZSM-5 modified by metal (Fe,Cu) oxides

    Science.gov (United States)

    Hu, Yanan; Liu, Jiangping; Cheng, Jinhuan; Wang, Langlang; Tao, Lei; Wang, Qi; Wang, Xueqian; Ning, Ping

    2018-01-01

    In this work, a series of metal oxides (Fe,Cu) modified HZSM-5 catalysts were synthesized by incipient-wetness impregnation method and then characterized by XRD, N2 adsorption-desorption, H2-TPR, NH3-TPD, UV-vis, FT-IR and XPS measurements. The catalytic hydrolysis and oxidation behaviors toward HCN were investigated. The results indicated that the Fe-Cu/HZSM-5 catalysts exhibited more excellent performence on coupling catalytic hydrolysis and oxidation of HCN than HZSM-5, Fe/HZSM-5, Cu/HZSM-5, and both nearly 100% HCN conversion and 80% N2 selectivity were obtained at about 250 °C. The improved catalytic performance could be ascribed to the creation of highly dispersed iron and copper composites on the surface of the HZSM-5 support, the excellent redox and regulated acid properties of the active ingredients. Moreover, the highly N2 selectivity could be attributed to the good interaction between the Fe and Cu nanocomposites which was facilitated to the NH3-SCR (selective catalytic reduction of NO by NH3) reaction.

  9. Effect of Copper and Zirconium Addition on Properties of Fe-Co-Si-B-Nb Bulk Metallic Glasses

    Science.gov (United States)

    Ikram, Haris; Khalid, Fazal Ahmad; Akmal, Muhammad; Abbas, Zameer

    2017-07-01

    In this research work, iron-based bulk metallic glasses (BMGs) have been fabricated, characterized and compared with Fe-Si alloy. BMG alloys of composition ((Fe0.6Co0.4)0.75B0.20Si0.05)96Nb4) were synthesized by suction casting technique using chilled copper die. Effect of copper and zirconium addition on magnetic, mechanical, thermal and electrochemical behavior of ((Fe0.6Co0.4)0.75B0.20Si0.05)96Nb4 BMGs was investigated. Furthermore, effect of annealing on nano-crystallization and subsequently on magnetic and mechanical behavior was also analyzed. Amorphousness of structure was evidenced by XRD analysis and microscopic visualization, whereas nano-crystallization behavior was identified by peak broadening of XRD patterns. Magnetic properties, measured by vibrating sample magnetometer, were found to be improved for as-cast BMG alloys by copper addition and further enhanced by nano-crystallization after annealing. Mechanical properties were observed to be increased by zirconium addition while slightly declined by copper addition. Potentiodynamic polarization analysis manifested the positive role of zirconium in enhancing corrosion resistance of BMGs in acidic, basic and brine mediums. Moreover, mechanical properties and corrosion analysis results affirmed the superiority of BMG alloys over Fe-Si alloy.

  10. Investigation on fuel-cladding chemical interaction in metal fuel for FBR. Reaction of rare earth elements with Fe-Cr alloy

    International Nuclear Information System (INIS)

    Inagaki, Kenta; Ogata, Takanari

    2010-01-01

    Rare-earth fission product (FP) elements generated in the metal fuel interact with cladding alloy and result in the wastage of the cladding (Fuel-Cladding Chemical Interaction (FCCI)). To evaluate FCCI quantitatively, several influential factors must be considered. They are temperature, temperature gradient, time, composition of the cladding and the behavior of rare-earth FP. In this research, the temperature and time dependencies are investigated with tests in the simplified system. Fe-12wt%Cr was used as stimulant material of cladding and rare-earth alloy 13La -24Ce -12Pr -39Nd -12Sm (RE) as a rare-earth FP. A diffusion couple Fe-Cr/RE was made and annealed at 923K, 853K, 773K or 693K. The structures of reaction layers were analyzed with Electron Probe Micro Analyzer (EPMA) and the details of the structures were clarified. The width of the reaction layer in the Fe-Cr alloy grew in proportion to the square root of time. The reaction rate constants K=(square of the width of reaction layer / time) were evaluated. It was confirmed that the relation between K and the inverse of the temperature showed linearity above 773 K. (author)

  11. An Efficient Bifunctional Electrocatalyst for a Zinc-Air Battery Derived from Fe/N/C and Bimetallic Metal-Organic Framework Composites.

    Science.gov (United States)

    Wang, Mengfan; Qian, Tao; Zhou, Jinqiu; Yan, Chenglin

    2017-02-15

    Efficient bifunctional electrocatalysts with desirable oxygen activities are closely related to practical applications of renewable energy systems including metal-air batteries, fuel cells, and water splitting. Here a composite material derived from a combination of bimetallic zeolitic imidazolate frameworks (denoted as BMZIFs) and Fe/N/C framework was reported as an efficient bifunctional catalyst. Although BMZIF or Fe/N/C alone exhibits undesirable oxygen reaction activity, a combination of these materials shows unprecedented ORR (half-wave potential of 0.85 V as well as comparatively superior OER activities (potential@10 mA cm -2 of 1.64 V), outperforming not only a commercial Pt/C electrocatalyst but also most reported bifunctional electrocatalysts. We then tested its practical application in Zn-air batteries. The primary batteries exhibit a high peak power density of 235 mW cm -2 , and the batteries are able to be operated smoothly for 100 cycles at a curent density of 10 mA cm -2 . The unprecedented catalytic activity can be attritued to chemical coupling effects between Fe/N/C and BMZIF and will aid the development of highly active electrocatalysts and applications for electrochemical energy devices.

  12. Size effect study in magnetoelectric BiFeO 3 system

    Indian Academy of Sciences (India)

    N) of magnetoelectric BiFeO3 system. Novel wet chemical route has been developed to produce fine particles of BiFeO3 with controlled size and size distribution. Unlike other oxide systems, lattice volume contraction has been observed with ...

  13. Retention Mechanisms of Citric Acid in Ternary Kaolinite-Fe(III)-Citrate Acid Systems Using Fe K-edge EXAFS and L3,2-edge XANES Spectroscopy

    Science.gov (United States)

    Yang, Jianjun; Wang, Jian; Pan, Weinan; Regier, Tom; Hu, Yongfeng; Rumpel, Cornelia; Bolan, Nanthi; Sparks, Donald

    2016-01-01

    Organic carbon (OC) stability in tropical soils is strongly interlinked with multivalent cation interaction and mineral association. Low molecular weight organic acids (LMWOAs) represent the readily biodegradable OC. Therefore, investigating retention mechanisms of LMWOAs in mineral-cation-LMWOAs systems is critical to understanding soil C cycling. Given the general acidic conditions and dominance of kaolinite in tropical soils, we investigated the retention mechanisms of citric acid (CA) in kaolinite-Fe(III)-CA systems with various Fe/CA molar ratios at pH ~3.5 using Fe K-edge EXAFS and L3,2-edge XANES techniques. With Fe/CA molar ratios >2, the formed ferrihydrite mainly contributed to CA retention through adsorption and/or coprecipitation. With Fe/CA molar ratios from 2 to 0.5, ternary complexation of CA to kaolinite via a five-coordinated Fe(III) bridge retained higher CA than ferrihydrite-induced adsorption and/or coprecipitation. With Fe/CA molar ratios ≤0.5, kaolinite-Fe(III)-citrate complexation preferentially occurred, but less CA was retained than via outer-sphere kaolinite-CA complexation. This study highlighted the significant impact of varied Fe/CA molar ratios on CA retention mechanisms in kaolinite-Fe(III)-CA systems under acidic conditions, and clearly showed the important contribution of Fe-bridged ternary complexation on CA retention. These findings will enhance our understanding of the dynamics of CA and other LMWOAs in tropical soils. PMID:27212680

  14. Wear Behavior and Self Tribofilm Formation of Infiltration-Type TiC/FeCrWMoV Metal Ceramics Under Dry Sliding Conditions

    DEFF Research Database (Denmark)

    Wang, Yanjun; Yang, Zhenyu; Han, Liying

    2015-01-01

    A new type high temperature self-lubrication TiC/FeCrWMoV metal ceramic was fabricated successfully by applying an innovating technology which molten solid lubricant (60Pb40Sn-15Ag-0.5RE) was infiltrated into metal ceramic preforms with an interpenetrating network using a vacuum high pressure...

  15. High adsorptive γ-AlOOH(boehmite)@SiO2/Fe3O4 porous magnetic microspheres for detection of toxic metal ions in drinking water.

    Science.gov (United States)

    Wei, Yan; Yang, Ran; Zhang, Yong-Xing; Wang, Lun; Liu, Jin-Huai; Huang, Xing-Jiu

    2011-10-21

    γ-AlOOH(boehmite)@SiO(2)/Fe(3)O(4) porous magnetic microspheres with high adsorption capacity toward heavy metal ions were found to be useful for the simultaneous and selective electrochemical detection of five metal ions, such as ultratrace zinc(II), cadmium(II), lead(II), copper(II), and mercury(II), in drinking water.

  16. Phase Equilibria of the Fe-Ni-Sn Ternary System at 270°C

    Science.gov (United States)

    Huang, Tzu-Ting; Lin, Shih-Wei; Chen, Chih-Ming; Chen, Pei Yu; Yen, Yee-Wen

    2016-12-01

    The Fe-42 wt.% Ni alloy, also known as a 42 invar alloy (Alloy 42), is used as a lead-frame material because its thermal expansion coefficient is much closer to Si substrate than Cu or Ni substrates. In order to enhance the wettability between the substrate and solder, the Sn layer was commonly electroplated onto the Alloy 42 surface. A clear understanding of the phase equilibria of the Fe-Ni-Sn ternary system is necessary to ensure solder-joint reliability between Sn and Fe-Ni alloys. To determine the isothermal section of the Fe-Ni-Sn ternary system at 270°C, 26 Fe-Ni-Sn alloys with different compositions were prepared. The experimental results confirmed the presence of the Fe3Ni and FeNi phases at 270°C. Meanwhile, it observed that the isothermal section of the Fe-Ni-Sn ternary system was composed of 11 single-phase regions, 19 two-phase regions and nine tie-triangles. Moreover, no ternary compounds were found in the Fe-Ni-Sn system at 270°C.

  17. Rapid Adsorption of Heavy Metals by Fe3O4/Talc Nanocomposite and Optimization Study Using Response Surface Methodology

    Science.gov (United States)

    Kalantari, Katayoon; Ahmad, Mansor B.; Masoumi, Hamid Reza Fard; Shameli, Kamyar; Basri, Mahiran; Khandanlou, Roshanak

    2014-01-01

    Fe3O4/talc nanocomposite was used for removal of Cu(II), Ni(II), and Pb(II) ions from aqueous solutions. Experiments were designed by response surface methodology (RSM) and a quadratic model was used to predict the variables. The adsorption parameters such as adsorbent dosage, removal time, and initial ion concentration were used as the independent variables and their effects on heavy metal ion removal were investigated. Analysis of variance was incorporated to judge the adequacy of the models. Optimal conditions with initial heavy metal ion concentration of 100, 92 and 270 mg/L, 120 s of removal time and 0.12 g of adsorbent amount resulted in 72.15%, 50.23%, and 91.35% removal efficiency for Cu(II), Ni(II), and Pb(II), respectively. The predictions of the model were in good agreement with experimental results and the Fe3O4/talc nanocomposite was successfully used to remove heavy metals from aqueous solutions. PMID:25050784

  18. Optimization of film synthesized rare earth transition metal permanent magnet systems

    International Nuclear Information System (INIS)

    Cadieu, F.J.

    1992-01-01

    Progress is reported in three areas: high coercivity Sm-Fe-Ti-V, Sm-Fe-Zr, and two element Sm-Fe Sm 5 (Fe,T) 17 type crystalline phases; ThMn 12 type pseudobinary SmFe 12-x T x (0≤x≤1.5); and sputter process control for the synthesis of precisely textured rare earth-transition metal magnetic films

  19. Determination of concentration of heavy metals (Pb, Cd, Fe) in animal tissues using atomic absorption spectrometry

    International Nuclear Information System (INIS)

    RAZAFINTSALAMA, V.T.

    2009-01-01

    Heavy metals are classified among the inorganic compounds. The latter type of metal is found in rocks, fertilizers, urban mud but may also originate from the atmospheric pollution. A particular characteristic of heavy metals is their bioaccumulation in the food chain. Therefore, lead and cadmium, which are classified as heavy metals may be easily found in animal products and can lead to food poisoning if their concentrations are higher than the maximum permissible values as requested by international agencies such as the c odex alimentarius . The values are set down and differ according to types of food for human consuption and the trading companies take action accordingly. Therefore, it is necessary to set up a quality control system through analytical laboratory measurements and testings. This study underlies the method of determination of lead, cadmium and iron in animal tissues by atomic absorption spectrometry. The results showed that the method is sensitive and reliable. For each analyte, the Z-score lies between -2 and 2, indicating that the method is working properly. The analytical results showed that: (i) only beef and chicken meats and beef liver contain lead [0,09μg.g - 1; 0,29μg.g - 1]. The limit value of 0,1μg.g - 1 is almost reached in beef and chicken meats, (ii) as far as cadmium is concerned, the five studied samples contain this analyte [0,02μg.g - 1; 0,9μg.g - 1]. Except the chicken liver of which the concentration (0,15μg.g - 1) exceeds the maximum permissible value (0,1μg.g - 1), the others are in conformity with the standards and appropriate to be consumed,(iii) iron is higher in the liver and kidney samples: beef liver 282mg.g - 1, chicken liver 250 mg.g - 1, pork kidney 247mg.g - 1. The study also showed that the calcium concentration in animal tissues is low and they can be classified as poor-calcium food. [fr

  20. Recent materials compatibility studies in refractory metal-alkali metal systems for space power applications.

    Science.gov (United States)

    Harrison, R. W.; Hoffman, E. E.; Davies, R. L.

    1972-01-01

    Advanced Rankine and other proposed space power systems utilize refractory metals in contact with both single-phase and two-phase alkali metals at elevated temperatures. A number of recent compatibility experiments are described which emphasize the excellent compatibility of refractory metals with the alkali metals, lithium, sodium, and potassium, under a variety of environmental conditions. The alkali metal compatibilities of tantalum-, columbium-, molybdenum-, and tungsten-base alloys are discussed.

  1. Microbial Mineral Transformations at the Fe(II)/Fe(III) Redox Boundary for Solid Phase Capture of Strontium and Other Metal/Radionuclide Contaminants

    Energy Technology Data Exchange (ETDEWEB)

    F. G. Ferris; E. E. Roden

    2000-01-31

    The migration of {sup 90}Sr in groundwater is a significant environmental concern at former nuclear weapons production sites in the US and abroad. Although retardation of {sup 90}Sr transport relative to mean groundwater velocity is known to occur in contaminated aquifers, Sr{sup 2+} does not sorb as strongly to iron oxides and other mineral phases as do other metal-radionuclides contaminants. Thus, some potential exists for extensive {sup 90}Sr migration from sources of contamination. Chemical or biological processes capable of retarding or immobilizing Sr{sup 2+} in groundwater environments are of interest from the standpoint of understanding controls on subsurface Sr{sup 2+} migration. In addition, it may be possible to exploit such processes for remediation of subsurface Sr contamination. In this study the authors examined the potential for the solid phase sorption and incorporation of Sr{sup 2+} into carbonate minerals formed during microbial Fe(III) oxide reduction as a first step toward evaluating whether this process could be used to promote retardation of {sup 90}Sr migrations in anaerobic subsurface environments. The demonstration of Sr{sup 2+} capture in carbonate mineral phases formed during bacterial HFO reduction and urea hydrolysis suggests that microbial carbonate mineral formation could contribute to Sr{sup 2+} retardation in groundwater environments. This process may also provide a mechanism for subsurface remediation of Sr{sup 2+} and other divalent metal contaminants that form insoluble carbonate precipitates.

  2. Microbial Mineral Transformations at the Fe(II)/Fe(III) Redox Boundary for Solid Phase Capture of Strontium and Other Metal/Radionuclide Contaminants

    International Nuclear Information System (INIS)

    Ferris, F.G.; Roden, E.E.

    2000-01-01

    The migration of 90 Sr in groundwater is a significant environmental concern at former nuclear weapons production sites in the US and abroad. Although retardation of 90 Sr transport relative to mean groundwater velocity is known to occur in contaminated aquifers, Sr 2+ does not sorb as strongly to iron oxides and other mineral phases as do other metal-radionuclides contaminants. Thus, some potential exists for extensive 90 Sr migration from sources of contamination. Chemical or biological processes capable of retarding or immobilizing Sr 2+ in groundwater environments are of interest from the standpoint of understanding controls on subsurface Sr 2+ migration. In addition, it may be possible to exploit such processes for remediation of subsurface Sr contamination. In this study the authors examined the potential for the solid phase sorption and incorporation of Sr 2+ into carbonate minerals formed during microbial Fe(III) oxide reduction as a first step toward evaluating whether this process could be used to promote retardation of 90 Sr migrations in anaerobic subsurface environments. The demonstration of Sr 2+ capture in carbonate mineral phases formed during bacterial HFO reduction and urea hydrolysis suggests that microbial carbonate mineral formation could contribute to Sr 2+ retardation in groundwater environments. This process may also provide a mechanism for subsurface remediation of Sr 2+ and other divalent metal contaminants that form insoluble carbonate precipitates

  3. Effect of noble metals in the decomposition of nitrous oxide over Fe-ferrierites

    Czech Academy of Sciences Publication Activity Database

    Sobalík, Zdeněk; Jíša, Kamil; Kaucký, Dalibor; Vondrová, Alena; Tvarůžková, Zdenka; Nováková, Jana

    2007-01-01

    Roč. 113, 3-4 (2007), s. 124-129 ISSN 1011-372X R&D Projects: GA AV ČR 1ET400400413 Institutional research plan: CEZ:AV0Z40400503 Keywords : Fe, Pt, Rh, Ru-ferrierite * synergy effects in Fe/Me-ferrierites * N2O decomposition Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 1.883, year: 2007

  4. Ab Initio Molecular Dynamics of Uranium Incorporated in Goethite (α-FeOOH): Interpretation of X-ray Absorption Spectroscopy of Trace Polyvalent Metals.

    Science.gov (United States)

    Kerisit, Sebastien; Bylaska, Eric J; Massey, Michael S; McBriarty, Martin E; Ilton, Eugene S

    2016-11-21

    Incorporation of economically or environmentally consequential polyvalent metals into iron (oxyhydr)oxides has applications in environmental chemistry, remediation, and materials science. A primary tool for characterizing the local coordination environment of such metals, and therefore building models to predict their behavior, is extended X-ray absorption fine structure spectroscopy (EXAFS). Accurate structural information can be lacking yet is required to constrain and inform data interpretation. In this regard, ab initio molecular dynamics (AIMD) was used to calculate the local coordination environment of minor amounts of U incorporated in the structure of goethite (α-FeOOH). U oxidation states (VI, V, and IV) and charge compensation schemes were varied. Simulated trajectories were used to calculate the U L III -edge EXAFS function and fit experimental EXAFS data for U incorporated into goethite under reducing conditions. Calculations that closely matched the U EXAFS of the well-characterized mineral uraninite (UO 2 ), and constrained the S 0 2 parameter to be 0.909, validated the approach. The results for the U-goethite system indicated that U(V) substituted for structural Fe(III) in octahedral uranate coordination. Charge balance was achieved by the loss of one structural proton coupled to addition of one electron into the solid (-1 H + , +1 e - ). The ability of AIMD to model higher energy states thermally accessible at room temperature is particularly relevant for protonated systems such as goethite, where proton transfers between adjacent octahedra had a dramatic effect on the calculated EXAFS. Vibrational effects as a function of temperature were also estimated using AIMD, allowing separate quantification of thermal and configurational disorder. In summary, coupling AIMD structural modeling and EXAFS experiments enables modeling of the redox behavior of polyvalent metals that are incorporated in conductive materials such as iron (oxyhydr)oxides, with

  5. Systems and methods for producing metal clusters; functionalized surfaces; and droplets including solvated metal ions

    Science.gov (United States)

    Cooks, Robert Graham; Li, Anyin; Luo, Qingjie

    2017-08-01

    The invention generally relates to systems and methods for producing metal clusters; functionalized surfaces; and droplets including solvated metal ions. In certain aspects, the invention provides methods that involve providing a metal and a solvent. The methods additionally involve applying voltage to the solvated metal to thereby produce solvent droplets including ions of the metal containing compound, and directing the solvent droplets including the metal ions to a target. In certain embodiments, once at the target, the metal ions can react directly or catalyze reactions.

  6. The effect of chemical composition and granulation of Fe - based fillers on properties of metal resinous composite

    International Nuclear Information System (INIS)

    Janecki, J.; Dasiewicz, J.; Pawelec, Z.

    2000-01-01

    In this paper the authors present metal-resinous composites with Fe based fillers of various element constitution and granulation. The analysis of influence of filler type on coefficient of linear thermal expansion of composite materials was performed. Friction and wear tests (composite-bronze and composite-steel pairs) were carried out. It was stated that the thinner granulation of main filler has a positive effect on coefficient of linear thermal expansion and friction/wear characteristics. The presence of copper, nickel and molybdenum in the filler is beneficial for some properties of the composite. (author)

  7. 29 CFR 1926.758 - Systems-engineered metal buildings.

    Science.gov (United States)

    2010-07-01

    ... 29 Labor 8 2010-07-01 2010-07-01 false Systems-engineered metal buildings. 1926.758 Section 1926... Systems-engineered metal buildings. (a) All of the requirements of this subpart apply to the erection of systems-engineered metal buildings except §§ 1926.755 (column anchorage) and 1926.757 (open web steel...

  8. Leaching of rapidly quenched Al65Cu20Fe15 quasicrystalline ribbons

    Indian Academy of Sciences (India)

    2017-12-06

    Dec 6, 2017 ... softening tendency and high hardness. When prepared by conventional melting and casting, the QC phase in Al–Cu–. Fe system exhibits a peritectic reaction among AlFe, Al3Fe ... stability, easy forming ability of the metallic nanoparticles on ... Fe3O4 (magnetite, JCPDS Number 65-3107), with lattice.

  9. Regularity in the formation of compounds in ternary R-Me-Sn systems, R - REM, Me - Fe, Co, Ni, Cu

    International Nuclear Information System (INIS)

    Skolozdra, R.V.; Komarovskaya, L.P.; Koretskaya, O.Eh.

    1992-01-01

    For the ternary alloy systems of (La, Y, Gd, Lu)-Fe-Sn, (Ce, Y, Gd)-Co-Sn, (Ce, Y, Gd, Lu)-Ni-Sn and (Pr, Gd, Lu)-Cu-Sn isothermal sections of phase diagrams were plotted within the range of 670 to 870 K. It was revealed that substitution of transition metal in the kFe-Co-Ni-Cu series led to changes both in a number of ternary stannides and their structural types. A tendency was observed in change of stannide numbers depending on quantity ratio of R and Me components. Crystallochemical analysis of compounds obtained showed that they could be treated as interstitial structures or lsuperstructures with respect to them. The results of magnetic properties measurements were used for explanation of structural features of ternary compounds considered

  10. 58Fe AND 54Cr IN EARLY SOLAR SYSTEM MATERIALS

    International Nuclear Information System (INIS)

    Wang, Kun; Moynier, Frederic; Podosek, Frank; Foriel, Julien

    2011-01-01

    Stepwise dissolution of primitive meteorites exhibits large 54 Cr anomalies but no collateral effects on 58 Fe and 48 Ca, two other neutron-rich nuclides from the iron peak. These results suggest that 54 Cr must have been produced in particular zones of the rare Type Ia supernovae or that 48 Ca and/or 58 Fe were produced together in Type II supernovae and were chemically separated into some mineral phase that favors Cr over Ca and Fe, and it is the dissolution properties of that phase that is driving the isotopic effect in leaching. The recent findings of nanometer-size oxide grains with very large 54 Cr excesses favored the latter scenario for the origin of the mono-isotopic Cr isotopic effect. In addition, the absence of isotopic variations in the 58 Fe/ 54 Fe ratio at the mineral scale confirms that the short-lived nuclide 60 Fe (T 1/2 = 2.62 Myr) was homogeneously distributed to a less than 15% dispersion in the early solar nebula.

  11. 58Fe and 54Cr in Early Solar System Materials

    Science.gov (United States)

    Wang, Kun; Moynier, Frederic; Podosek, Frank; Foriel, Julien

    2011-10-01

    Stepwise dissolution of primitive meteorites exhibits large 54Cr anomalies but no collateral effects on 58Fe and 48Ca, two other neutron-rich nuclides from the iron peak. These results suggest that 54Cr must have been produced in particular zones of the rare Type Ia supernovae or that 48Ca and/or 58Fe were produced together in Type II supernovae and were chemically separated into some mineral phase that favors Cr over Ca and Fe, and it is the dissolution properties of that phase that is driving the isotopic effect in leaching. The recent findings of nanometer-size oxide grains with very large 54Cr excesses favored the latter scenario for the origin of the mono-isotopic Cr isotopic effect. In addition, the absence of isotopic variations in the 58Fe/54Fe ratio at the mineral scale confirms that the short-lived nuclide 60Fe (T 1/2 = 2.62 Myr) was homogeneously distributed to a less than 15% dispersion in the early solar nebula.

  12. Structural and magnetic properties of Fe{sub x}Ni{sub 100−x} alloys synthesized using Al as a reducing metal

    Energy Technology Data Exchange (ETDEWEB)

    Srakaew, N. [Department of Physics, Faculty of Science, Kasetsart University, Bangkok 10900 (Thailand); Jantaratana, P., E-mail: fscipsj@ku.ac.th [Department of Physics, Faculty of Science, Kasetsart University, Bangkok 10900 (Thailand); Nipakul, P. [Department of Physics, Faculty of Science, Kasetsart University, Bangkok 10900 (Thailand); Sirisathitkul, C. [Molecular Technology Research Unit, School of Science, Walailak University, Nakhon Si Thammarat 80161 (Thailand)

    2017-08-01

    Highlights: • Reduction by aluminum is a simple and safe route to synthesize iron-nickel alloys. • Alloy compositions with up to 90 at.% Fe can be obtained with minimal oxidation. • Morphology and magnetic properties are varied with the alloy composition. - Abstract: Iron-nickel (Fe-Ni) alloys comprising nine different compositions were rapidly synthesized from the redox reaction using aluminum foils as the reducing metal. Compared with conventional chemical syntheses, this simple approach is relatively safe and allows control over the alloy morphology and magnetic behavior as a function of the alloy composition with minimal oxidation. For alloys having low (10%–30%) Fe content the single face-centered cubic (FCC) FeNi{sub 3} phase was formed with nanorods aligned in the (1 1 1) crystalline direction on the cluster surface. This highly anisotropic morphology gradually disappeared as the Fe content was raised to 40%–70% with the alloy structure possessing a mixture of FCC FeNi{sub 3} and body-centered cubic (BCC) Fe{sub 7}Ni{sub 3}. The FCC phase was entirely replaced by the BCC structure upon further increase the Fe content to 80%–90%. The substitution of Ni by Fe in the crystals and the dominance of the BCC phase over the FCC structure gave rise to enhanced magnetization. By contrast, the coercive field decreased as a function of increasing Fe because of the reduction in shape anisotropy and the rise of saturation magnetization.

  13. Thermolysis characteristics of salts of o-phthalic acid with the formation of Fe, Co, Ni, Cu metal particles

    Science.gov (United States)

    Yudanova, L. I.; Logvinenko, V. A.; Yudanov, N. F.; Rudina, N. A.; Ishchenko, A. V.; Korol'kov, I. V.; Semyannikov, P. P.; Sheludyakova, L. A.; Alferova, N. I.

    2016-06-01

    Studies of the thermolysis of ortho-[Ni(H2O)2(C8H4O4)](H2O)2, [Cu(H2O)(C8H4O4)], and acid [M(H2O)6](C8H5O4)2 (M(II) = Fe(II), Co(II), and Ni(II)), [Cu(H2O)2(C8H5O4)2] phthalates reveal that the solid products of their decomposition are composites with nanoparticles embedded in carbon-polymer matrices. Metallic nanoparticles with oxide nanoparticle impurities are detected in iron/cobalt polymer composites, while nickel/copper composites are composed of only metallic particles. It is found that nickel nanoparticles with the diameters of 6-8 nm are covered with disordered graphene layers, while the copperbased composite matrix contains spherical conglomerates (50-200 nm) with numerous spherical Cu particles (5-10 nm).

  14. Structural distortion on metal-insulator transition in ordered double perovskite Ca sub 2 FeReO sub 6

    CERN Document Server

    Oikawa, K; Kato, H; Tokura, Y

    2003-01-01

    The crystal and magnetic structures of an ordered double perovskite, Ca sub 2 FeReO sub 6 , were studied by high-resolution neutron powder diffraction as a function of the temperature from 7 K to 550 K. All of the diffraction data were precisely refined by the Rietveld method, and we confirmed a structural phase transition at around 140 K where the metal-insulator transition occurs from ferrimagnetic metal (FM) to ferrimagnetic insulator (FI) phases. At this temperature, there exists a change in the distortion direction of [ReO sub 6] octahedra together with a spin reorientation, which strongly supports the occurrence of orbital ordering of the t sub 2 sub g electrons. FM and FI phases coexist in a narrow temperature range at around 140 K, which is typically seen in the first-order phase transition. A phase separation was not detected in our well-characterized sample. (author)

  15. Preliminary Results on the Surface of a New Fe-Based Metallic Material after “In Vivo” Maintaining

    Science.gov (United States)

    Săndulache, F.; Stanciu, S.; Cimpoeşu, N.; Stanciu, T.; Cimpoeșu, R.; Enache, A.; Baciu, R.

    2017-06-01

    Abstract A new Fe-based alloy was obtained using UltraCast melting equipment. The alloy, after mechanical processing, was implanted in five rabbit specimens (with respect for the “in-bone” procedure). After 30 days of implantation the samples were recovered and analyzed by weight and surface state meanings. Scanning electron microscopy technique was used to determine the new compounds morphology from the metallic surface and X-ray dispersive energy spectroscopy for chemical analyze results. A bond between the metallic material and biological material of the bone was observed through increasing of sample weight and by SEM images. After the first set of tests, as the samples were extracted and biologically cleaned, the samples were ultrasonically cleaned and re-analyzed in order to establish the stability of the chemical compounds.

  16. Conformational adaptation of 2H-Tetraphenylporphyrin at Fe/Si(1 0 0 interface during metalation

    Directory of Open Access Journals (Sweden)

    Chhagan Lal

    2014-01-01

    Full Text Available Many recent studies have highlighted the possibility to tailor the physical and chemical properties of porphyrin at the molecular level to design novel catalysts, sensors and devices with applications in electronics, opto-electronics, etc. In the present work we study the electronic properties of 2H-Tetraphenylporphyrin (2H-TPP on iron (Fe and iron silicide (Fe3Si onto Si (1 0 0 substrate using X-ray and Ultraviolet photoelectron spectroscopy (XPS & UPS. The results revealed that the iron atom is coordinated by TPP molecules at Fe/Si system. XPS results provide evidence of the iron coordination with TPP molecules. The UPS analysis show the fine structure in the electronic spectra related to HOMO states below the Fermi level.

  17. Polarization fatigue of BiFeO3 films with ferromagnetic metallic electrodes

    Directory of Open Access Journals (Sweden)

    Chen Chen

    2017-05-01

    Full Text Available BiFeO3 (BFO thin films were epitaxially grown on (001 SrTiO3 substrates using LaNiO3 as bottom electrode by pulsed laser deposition. The ferroelectric properties of BFO layer with ferromagnetic Ni21Fe79 (NiFe or non-magnetic Pt electrode are investigated. Well saturated polarization-electric field (P-E hysteresis loops are observed. Significant fatigue and associated drastic decrease in switchable polarization have been observed with cycling number exceeds 106, which can be explained by the domain wall pinning due to the oxygen vacancies trapping. With increasing cycle number to above 107, the polarization is rejuvenated. The polarization for BFO layer with NiFe electrode recovers to the initial value, while only about 75% of initial polarization is recovered for BFO layer with Pt electrode. Furthermore, the imprint is alleviated and the P-E hysteresis loops become more symmetric after the polarization recovery. The difference can be understood by the different interface state of NiFe/BFO and Pt/BFO.

  18. A Multivariate Analysis of Metal Concentrations in Two Fish Species of the Nyl River System, Limpopo Province, South Africa.

    Science.gov (United States)

    Musa, R; Gerber, R; Greenfield, R

    2017-06-01

    Increased toxicity due to high metal concentrations may hinder the ecological integrity of aquatic ecosystems in sustaining life. The non-biodegradable nature of metals may result in bioaccumulation in aquatic organisms. Due to ecological and social aspects it is imperative for monitoring schemes to identify possible impacts to the systems integrity. This paper discusses accumulation patterns of seven metals (Al, Cr, Cu, Fe, Mn, Sr and Zn) in tissues of two fish species, namely Clarias gariepinus and Oreochromis mossambicus at two selected sites, the first located upstream of Modimolle (NRS1), and the second located downstream of the town (NRS2). Gills, liver, muscle and skin tissues were analysed for metal concentrations using standard microwave digestion and inductively coupled plasma mass spectrometry techniques. Statistical results indicated higher concentrations of metals at NRS2 in comparison to NRS1, indicating that Modimolle plays a potential role in introducing metals into the aquatic system.

  19. A procedure for calibration and validation of FE modelling of laser-assisted metal to polymer direct joining

    Science.gov (United States)

    Lambiase, F.; Genna, S.; Kant, R.

    2018-01-01

    The quality of the joints produced by means of Laser-Assisted Metal to Polymer direct joining (LAMP) is strongly influenced by the temperature field produced during the laser treatment. The main phenomena including the adhesion of the plastic to the metal sheet and the development of bubbles (on the plastic surface) depend on the temperature reached by the polymer at the interface. Such a temperature should be higher than the softening temperature, but lower than the degradation temperature of the polymer. However, the temperature distribution is difficult to be measured by experimental tests since the most polymers (which are transparent to the laser radiation) are often opaque to the infrared wavelength. Thus, infrared analysis involving pyrometers and infrared camera is not suitable for this purpose. On the other hand, thermocouples are difficult to be placed at the interface without influencing the temperature conditions. In this paper, an integrated approach involving both experimental measurements and a Finite Element (FE) model were used to perform such an analysis. LAMP of Polycarbonate and AISI304 stainless steel was performed by means of high power diode laser and the main process parameters i.e. laser power and scanning speed were varied. Comparing the experimental measurements and the FE model prediction of the thermal field, a good correspondence was achieved proving the suitability of the developed model and the proposed calibration procedure to be ready used for process design and optimization.

  20. Data and analyses of phase relations in the Ce-Fe-Sb ternary system.

    Science.gov (United States)

    Zhu, Daiman; Xu, Chengliang; Li, Changrong; Guo, Cuiping; Zheng, Raowen; Du, Zhenmin; Li, Junqin

    2018-02-01

    These data and analyses support the research article "Experimental study on phase relations in the Ce-Fe-Sb ternary system" Zhu et al. (2017) [1]. The data and analyses presented here include the experimental results of XRD, SEM and EPMA for the determination of the whole liquidus projection and the isothermal section at 823 K in the Ce-Fe-Sb system. All the results enable the understanding of the constituent phases and the solidification processes of the as-cast alloys as well as the phase relations and the equilibrium regions at 823 K in the Ce-Fe-Sb ternary system over the entire composition.

  1. Reversible Hydride Transfer to N,N'-Diarylimidazolinium Cations from Hydrogen Catalyzed by Transition Metal Complexes Mimicking the Reaction of [Fe]-Hydrogenase.

    Science.gov (United States)

    Hatazawa, Masahiro; Yoshie, Naoko; Seino, Hidetake

    2017-07-17

    [Fe]-hydrogenase is a key enzyme involved in methanogenesis and facilitates reversible hydride transfer from H 2 to N 5 ,N 10 -methenyltetrahydromethanopterin (CH-H 4 MPT + ). In this study, a reaction system was developed to model the enzymatic function of [Fe]-hydrogenase by using N,N'-diphenylimidazolinium cation (1 + ) as a structurally related alternative to CH-H 4 MPT + . In connection with the enzymatic mechanism via heterolytic cleavage of H 2 at the single metal active site, several transition metal complex catalysts capable of such activation were utilized in the model system. Reduction of 1[BF 4 ] to N,N'-diphenylimidazolidine (2) was achieved under 1 atm H 2 at ambient temperature in the presence of an equimolar amount of NEt 3 as a proton acceptor. The proposed catalytic pathways involved the generation of active hydride complexes and subsequent intermolecular hydride transfer to 1 + . The reverse reaction was accomplished by treatment of 2 with HNMe 2 Ph + as the proton source, where [(η 5 -C 5 Me 5 )Ir{(p-MeC 6 H 4 SO 2 )NCHPhCHPhNH}] was found to catalyze the formation of 1 + and H 2 with high efficiency. These results are consistent with the fact that use of 2,6-lutidine in the forward reaction or 2,6-lutidinium in the reverse reaction resulted in incomplete conversion. By combining these reactions using the above Ir amido catalyst, the reversible hydride transfer interconverting 1 + /H 2 and 2/H + was performed successfully. This system demonstrated the hydride-accepting and hydride-donating modes of biologically relevant N-heterocycles coupled with proton concentration. The influence of substituents on the forward and reverse reactivities was examined for the derivatives of 1 + and 2 bearing one para-substituted N-phenyl group.

  2. Percolation threshold of granular metal-dielectric nanocomposites (FeCoZr)x(CaF2)1-x produced in atmosphere of argon and oxygen

    Science.gov (United States)

    Bondariev, Vitalii

    2017-08-01

    The paper presents temperature-frequency dependencies of conductivity of the granular metal-dielectric nanocomposites (FeCoZr)x(CaF2)100-x. A series of nanocomposite samples with a different metallic phase content from range x = 41.3 - 86.1 at.% produced by twosources ion-beam sputtering in mixed atmosphere of argon and oxygen was tested. Analysis of results of temperature dependences of conductivity of the samples with metallic phase content x bellow 81.8 at.% obtained immediately after producing showed that nanocomposites (FeCoZr)x(CaF2)100-x exhibit dielectric properties, namely conductivity increases with the increase of measurement temperature. At the metal phase content x = 86,1 at.% inverse relationship of conductivity was observed, which menace that nanocomposite is characterized by metallic type of conductivity. Comparison of the conductivity at LNT (liquid nitrogen temperature) and at room temperature for different content of metallic phase allowed to set the percolation threshold for tested series of samples of nanocomposite (FeCoZr)x(CaF2)100-x. The change of type of conductivity from dielectric to metallic type takes place with metallic phase content about 82+/-0.2at.%.

  3. THE INFLUENCE OF pH TOWARDS MULTIPLE METAL ION ADSORPTION OF Cu(II, Zn(II, Mn(II, AND Fe(II ON HUMIC ACID

    Directory of Open Access Journals (Sweden)

    Buhani Buhani

    2010-06-01

    Full Text Available Multiple metal ions adsorption of Cu(II, Zn(II, Mn(II and Fe(II on humic acid with a batch method has been carried out at pH interaction of 3, 5, and 6. Concentration of metal ions in solution before and after interaction was analyzed with Atomic Absorption Spectrophotometer (AAS. Result showed that adsorption multiple metal ions of Cu(II, Zn(II, Mn(II, and Fe(II on humic acid is optimum at pH 5. Adsorption energies of the multiple metal ions Cu(II, Zn(II, Mn(II, and Fe(II on humic acid at pH 3, 5, and 6 are around 35.0 - 37.6 kJ/mole. In general, capacity of competition adsorption of the multiple metal ions has an order as follows; Cu(II < Fe(II < Zn(II < Mn(II.   Keywords: Humic acid, adsorption, multiple metal

  4. Analysis of thermal expansivity of iron (Fe) metal at ultra high ...

    Indian Academy of Sciences (India)

    In the present investigation we have explained the thermal and compression properties of HCP iron (Fe) at high pressure with variable temperature (isobars) and at high temperature with variable pressure (isotherm). The usual Tait equation of state is modified by incorporating the effect of thermal pressure. The calculated ...

  5. Adsorption of pentane isomers on metal-organic frameworks Cu-BTC and Fe-BTC

    Czech Academy of Sciences Publication Activity Database

    Zukal, Arnošt; Opanasenko, Maksym; Rubeš, M.; Nachtigall, P.; Jagiello, J.

    2015-01-01

    Roč. 243, APR 2014 (2015), s. 69-75 ISSN 0920-5861 R&D Projects: GA ČR GA14-07101S Institutional support: RVO:61388955 Keywords : Cu-BTC * Fe-BTC * adsorption Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 4.312, year: 2015

  6. Atomic alignment effect in the dissociative energy transfer reaction of metal carbonyls (Fe(CO)5, Ni(CO)4) with oriented Ar (3P2, M(J) = 2).

    Science.gov (United States)

    Ohoyama, H; Matsuura, Y

    2011-10-13

    The atomic alignment effect has been studied for the dissociative energy transfer reaction of metal carbonyls (Fe(CO)(5), Ni(CO)(4)) with the oriented Ar ((3)P(2), M(J) = 2). The emission intensity from the excited metal products (Fe*, Ni*) has been measured as a function of the atomic alignment in the collision frame. The selectivity of the atomic orbital alignment of Ar ((3)P(2), M(J) = 2) (rank 2 moment, a(2)) is found to be opposite for the two reaction systems; the Fe(CO)(5) reaction is favorable at the Π configuration (positive a(2)), while the Ni(CO)(4) reaction is favorable at the Σ configuration (negative a(2)). Moreover, a significant spin alignment effect (rank 4 moment, a(4)) is recognized only in the Ni(CO)(4) reaction. The atomic alignment effect turns out to be essentially different between the two reaction systems; the Fe(CO)(5) reaction is controlled by the configuration of the half-filled 3p atomic orbital of Ar ((3)P(2)) in the collision frame (L dependence), whereas the Ni(CO)(4) reaction is controlled by the configuration of the total angular moment J (including spin) of Ar ((3)P(2)) in the collision frame (J dependence). As the origin of J dependence observed only in the Ni(CO)(4) reaction, the correlation (and/or the interference) between two electron exchange processes via the electron rearrangements is proposed.

  7. Exploration of earth-abundant transition metals (Fe, Co, and Ni) as catalysts in unreactive chemical bond activations.

    Science.gov (United States)

    Su, Bo; Cao, Zhi-Chao; Shi, Zhang-Jie

    2015-03-17

    Activation of inert chemical bonds, such as C-H, C-O, C-C, and so on, is a very important area, to which has been drawn much attention by chemists for a long time and which is viewed as one of the most ideal ways to produce valuable chemicals. Under modern chemical bond activation logic, many conventionally viewed "inert" chemical bonds that were intact under traditional conditions can be reconsidered as novel functionalities, which not only avoids the tedious synthetic procedures for prefunctionalizations and the emission of undesirable wastes but also inspires chemists to create novel synthetic strategies in completely different manners. Although activation of "inert" chemical bonds using stoichiometric amounts of transition metals has been reported in the past, much more attractive and challenging catalytic transformations began to blossom decades ago. Compared with the broad application of late and noble transition metals in this field, the earth-abundant first-row transition-metals, such as Fe, Co, and Ni, have become much more attractive, due to their obvious advantages, including high abundance on earth, low price, low or no toxicity, and unique catalytic characteristics. In this Account, we summarize our recent efforts toward Fe, Co, and Ni catalyzed "inert" chemical bond activation. Our research first unveiled the unique catalytic ability of iron catalysts in C-O bond activation of both carboxylates and benzyl alcohols in the presence of Grignard reagents. The benzylic C-H functionalization was also developed via Fe catalysis with different nucleophiles, including both electron-rich arenes and 1-aryl-vinyl acetates. Cobalt catalysts also showed their uniqueness in both aromatic C-H activation and C-O activation in the presence of Grignard reagents. We reported the first cobalt-catalyzed sp(2) C-H activation/arylation and alkylation of benzo[h]quinoline and phenylpyridine, in which a new catalytic pathway via an oxidative addition process was demonstrated

  8. Investigation of the 600 C isothermal section of the Fe-Al-Ce ternary system

    Energy Technology Data Exchange (ETDEWEB)

    Zheng, Huiyun; Yin, Fucheng [Xiangtan Univ., Hunan (China). School of Materials Science and Engineering; Xiangtan Univ., Hunan (China). Key Laboratory of Materials Design and Preparation Technology of Hunan Province; Li, Zhi [Xiangtan Univ., Hunan (China). School of Materials Science and Engineering; Xiangtan Univ., Hunan (China). Key Laboratory of Materials Design and Preparation Technology of Hunan Province; Xiangtan Univ., Hunan (China). Key Laboratory of Key Film Materials and Application for Equipment (Hunan province); Ji, Li [South China University of Technology, Guangdong (China). School of Materials Science and Engineering

    2017-01-15

    The isothermal section of the Fe-Al-Ce system at 600 C was determined by means of scanning electron microscopy coupled with energy dispersive spectroscopy and X-ray powder diffraction. Twenty three-phase regions were confirmed experimentally, and two three-phase regions could be deduced in this section. Five ternary compounds, i. e., τ{sub 1}, τ{sub 2}, τ{sub 3}, τ{sub 5}, and τ{sub 6}, exist at 600 C. The Fe{sub 2}Ce phase contains 6.6 at.% Al in the Fe-Al-Ce system. The Fe solubility in α-Al, αAl{sub 11}Ce{sub 3}, αAl{sub 3}Ce, Al{sub 2}Ce, AlCe, and AlCe{sub 3} is approximately 1.7 at.%, 1.1 at.%, 1.2 at.%, 1.3 at.%, 5.8 at.%, and 0.1 at.%, respectively, and the solubility of Ce in α-Al, FeAl{sub 3}, Fe{sub 2}Al{sub 5}, FeAl{sub 2}, and FeAl is approximately 0.1 at.%, 1.2 at.%, 1.9 at.%, 0.9 at.%, and 3.7 at.%, respectively.

  9. Ab initio molecular dynamics model for density, elastic properties and short range order of Co-Fe-Ta-B metallic glass thin films

    International Nuclear Information System (INIS)

    Hostert, C; Music, D; Schneider, J M; Bednarcik, J; Keckes, J; Kapaklis, V; Hjörvarsson, B

    2011-01-01

    Density, elastic modulus and the pair distribution function of Co-Fe-Ta-B metallic glasses were obtained by ab initio molecular dynamics simulations and measured for sputtered thin films using x-ray reflectivity, nanoindentation and x-ray diffraction using high energy photons. The computationally obtained density of 8.19 g cm -3 for Co 43 Fe 20 Ta 5.5 B 31.5 and 8.42 g cm -3 for Co 45.5 Fe 24 Ta 6 B 24.5 , as well as the Young’s moduli of 273 and 251 GPa, respectively, are consistent with our experiments and literature data. These data, together with the good agreement between the theoretical and the experimental pair distribution functions, indicate that the model established here is useful to describe the density, elasticity and short range order of Co-Fe-Ta-B metallic glass thin films. Irrespective of the investigated variation in chemical composition, (Co, Fe)-B cluster formation and Co-Fe interactions are identified by density-of-states analysis. Strong bonds within the structural units and between the metallic species may give rise to the comparatively large stiffness. (paper)

  10. Magneto-thermo-gravimetric technique to investigate the structural and magnetic properties of Fe-B-Nb-Y Bulk Metallic Glass

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Sangmin; Makino, Akihiro; Inoue, Akihisa [Department of Materials Science, Graduate School of Engineering, Tohoku University, Sendai 980-8579 (Japan); Masood, Ansar; Tamaki, Takahiko; Valter, Strom; Rao, K V, E-mail: smlee@imr.tohoku.ac.j [Royal Institute of Technology (KTH), SE-100 44 Stockhom (Sweden)

    2009-01-01

    Magneto-thermo-gravimetric (MTG) technique is highly informative about the changes in the magnetic state, as well as structural changes in a system, which cannot be often noticed in calorimetric measurements. We demonstrate the versatility of this technique in determining the magnetic transition temperature, and the subsequent crystallization process in a (Fe{sub 0.72}B{sub 0.24}Nb{sub 0.04}){sub 95.5}Y{sub 4.5} Bulk Metallic Glass (BMG). MTG and DSC analyses were carried out at the heating rate of 0.67 K/s from RT {approx}1170 K. As a result of the repeated MTG measurements, a magnetic 2nd amorphous phase was observed in the BMG sample, which could be the first measurement for the Magnetic Short Range Ordering (MSRO). Consequently, the MTG measurement is proved as the most convenient method for determining the various structural and magnetic transitions in a glassy material.

  11. Shape of growing crystals of primary phases in autectic alloys of Fe - Fe2B and Ni - Ni3B systems

    International Nuclear Information System (INIS)

    Tavadze, F.N.; Garibashvili, V.I.; Nakaidze, Sh.G.

    1983-01-01

    Shapes of Fe 2 B and Ni 3 B crystal growth in eutectic Fe-B and Ni-B system alloys are considered. Iron hemiboride primary crystals take the form of a plane-face phase boundary and inherit a tetragonal prismatic lattice. After the crystal attains the critical size the dendritic branching occurs resulting in formation of a typical sceleton dendrite. Comparison of data obtained with entropy of melting for Fe 2 B and Ni 3 B borides shows that FeB crystals during the growth should take the spherical form. It is stated that the shape of growing crystals in Fe-Fe 2 B and Ni-Ni 2 B eutectic colonies is determined by the shape of borides

  12. How Correlated is the FeSe /SrTiO3 System?

    Science.gov (United States)

    Mandal, Subhasish; Zhang, Peng; Ismail-Beigi, Sohrab; Haule, K.

    2017-08-01

    Recent observation of ˜10 times higher critical temperature in a FeSe monolayer compared with its bulk phase has drawn a great deal of attention because the electronic structure in the monolayer phase appears to be different than bulk FeSe. Using a combination of density functional theory and dynamical mean field theory, we find electronic correlations have important effects on the predicted atomic-scale geometry and the electronic structure of the monolayer FeSe on SrTiO3 . The electronic correlations are dominantly controlled by the Se-Fe-Se angle either in the bulk phase or the monolayer phase. But the angle sensitivity increases and the orbital differentiation decreases in the monolayer phase compared to the bulk phase. The correlations are more dependent on Hund's J than Hubbard U . The observed orbital selective incoherence to coherence crossover with temperature confirms the Hund's metallic nature of the monolayer FeSe. We also find electron doping by oxygen vacancies in SrTiO3 increases the correlation strength, especially in the dx y orbital by reducing the Se-Fe-Se angle.

  13. Nonequilibrium dynamics in an interacting Fe-C nanoparticle system

    DEFF Research Database (Denmark)

    Jönsson, P.; Hansen, Mikkel Fougt; Nordblad, P.

    2000-01-01

    Nonequilibrium dynamics in an interacting Fe-C nanoparticle sample, exhibiting a low-temperature spin-glass-like phase, has been studied by low-frequency ac susceptibility and magnetic relaxation experiments. The nonequilibrium behavior shows characteristic spin-glass features, but some qualitative...

  14. Testing Metallic Iron Filtration Systems for Decentralized Water Treatment at Pilot Scale

    Directory of Open Access Journals (Sweden)

    Raoul Tepong-Tsindé

    2015-03-01

    Full Text Available There are many factors to consider for the design of appropriate water treatment systems including: cost, the concentration and type of biological and/or chemical contamination, concentration limits at which contaminant(s are required to be removed, required flow rate, level of local expertise for on-going maintenance, and social acceptance. An ideal technology should be effective at producing clean, potable water; however it must also be low-cost, low-energy (ideally energy-free and require low-maintenance. The use of packed beds containing metallic iron (Fe0 filters has the potential to become a cheap widespread technology for both safe drinking water provision and wastewater treatment. Fe0 filters have been intensively investigated over the past two decades, however, sound design criteria are still lacking. This article presents an overview of the design of Fe0 filters for decentralized water treatment particularly in the developing world. A design for safe drinking water to a community of 100 people is also discussed as starting module. It is suggested that Fe0 filters have the potential for significant worldwide applicability, but particularly in the developing world. The appropriate design of Fe0 filters, however, is site-specific and dependent upon the availability of local expertise/materials.

  15. Powder alignment system for anisotropic bonded NdFeB Halbach cylinders \\ud

    OpenAIRE

    Zhu, Z.Q.; Xia, Z.P.; Atallah, K.; Jewell, G.W.; Howe, D.

    2000-01-01

    A Halbach cylinder, fabricated from pre-magnetized sintered NdFeB magnet segments, is proposed for the powder aligning system during the compression or injection moulding of anisotropic bonded Halbach oriented NdFeB ring magnets. The influence of leading design parameters of the powder aligning system, viz. the number of magnet segments per pole, their axial length and radial thickness, and their clearance from the mould, is investigated by finite element analysis, and validated experimentally

  16. Supramolecular Host-Guest System as Ratiometric Fe3+ Ion Sensor Based on Water-Soluble Pillar[5]arene.

    Science.gov (United States)

    Yao, Qianfang; Lü, Baozhong; Ji, Chendong; Cai, Yang; Yin, Meizhen

    2017-10-18

    Developing a specific, ratiometric, and reversible detection method for metal ions is significant to guard against the threat of metal-caused environmental pollution and organisms poisoning. Here a supramolecular host-guest system (WP5⊃G) based on water-soluble pillar[5]arene (WP5) and water-soluble quaternized perylene diimide derivative (G) was constructed. Morphological transformation was achieved during the process of adding WP5 into G aqueous solution, and a fluorescence "turn-off" phenomenon was observed which was caused by supramolecular photoinduced electron transfer (PET). Meanwhile, hydrophobic effect and electrostatic interaction played important roles in this supramolecular process, which was confirmed by isothermal titration calorimeter (ITC) and ζ potential experiments. Furthermore, the supramolecular host-guest system could be a "turn-on" fluorescent probe for Fe 3+ ion detection through the process of interdicting supramolecular PET. Moreover, the Fe 3+ ion detection showed specific, ratiometric, and reversible performances with a detection limit of 2.13 × 10 -7 M, which might have great potentials in biological and environmental monitoring.

  17. Nonprecious Metal Catalysts for Oxygen Reduction in Heterogeneous Aqueous Systems.

    Science.gov (United States)

    Gewirth, Andrew A; Varnell, Jason A; DiAscro, Angela M

    2018-01-31

    A comprehensive review of recent advances in the field of oxygen reduction electrocatalysis utilizing nonprecious metal (NPM) catalysts is presented. Progress in the synthesis and characterization of pyrolyzed catalysts, based primarily on the transition metals Fe and Co with sources of N and C, is summarized. Several synthetic strategies to improve the catalytic activity for the oxygen reduction reaction (ORR) are highlighted. Recent work to explain the active-site structures and the ORR mechanism on pyrolyzed NPM catalysts is discussed. Additionally, the recent application of Cu-based catalysts for the ORR is reviewed. Suggestions and direction for future research to develop and understand NPM catalysts with enhanced ORR activity are provided.

  18. Half-metallic behavior and electronic structure of Sr2CrMoO6 magnetic system

    International Nuclear Information System (INIS)

    Bonilla, C.M.; Landinez Tellez, D.A.; Arbey Rodriguez, J.; Vera Lopez, E.; Roa-Rojas, J.

    2007-01-01

    Complex perovskite materials with the A 2 BB'O 6 formula have been recently studied because of their peculiar magnetic and electronic properties. The origin of magnetism in the double perovskite Sr 2 FeMoO 6 brought these properties again into discussion. Recently, a new interaction mechanism was proposed for cases in which the hybridization of 3d and 2p levels of Mo with the 3d Fe levels is responsible for the half-metallic behavior in the Sr 2 FeMoO 6 material. We report on LAPW ab initio calculations within the generalized gradient approximation (GGA) to density functional theory (DFT) for another double perovskite, namely, Sr 2 CrMoO 6 . Our results show that this is also a half-metallic system. We correlate our results with an extension of the recent model proposed by Sarma to explain the conduction mechanism in this compound

  19. Transport of trace metals (Mn, Fe, Ni, Zn and Cd) in the western Arctic Ocean (Chukchi Sea and Canada Basin) in late summer 2012

    Science.gov (United States)

    Kondo, Yoshiko; Obata, Hajime.; Hioki, Nanako; Ooki, Atsushi; Nishino, Shigeto; Kikuchi, Takashi; Kuma, Kenshi

    2016-10-01

    Distributions of trace metals (Mn, Fe, Ni, Zn and Cd) in the western Arctic Ocean (Chukchi Sea and Canada Basin) in September 2012 were investigated to elucidate the mechanisms behind the transport of these metals from the Chukchi Shelf to the Canada Basin. Filtered (metal concentrations, respectively. We identified maxima in vertical profiles for the concentrations of D-Fe and TD-Fe, as well as for the other four analyzed trace metals, which occurred in the halocline and/or near-bottom waters. Concentration profiles of all trace metals except for Cd also tended to show peaks near the surface, which suggest that the inflow of low-salinity Pacific-origin water from the Bering Strait, as well as local fresh water inputs such as river water and melting sea-ice, influenced trace metal concentrations. The distribution patterns and concentration ranges were generally similar between the D and TD fractions for Ni, Zn and Cd, which indicate that Ni, Zn and Cd were present mainly in their dissolved forms, whereas the concentrations of TD-Fe and TD-Mn were generally higher than those of D-Fe and D-Mn, respectively. These results are consistent with the results of previous studies of this region. For both Fe and Mn, labile particulate (LP) concentrations (the difference between the TD and D fractions, which is acid-leachable fraction in the particles during storage at pH 1.5-1.6) were highest in the near-bottom waters of the Chukchi Shelf region. The relationships between the distance from the shelf break and the concentrations of trace metals revealed that Fe and Mn concentrations in halocline waters tended to decrease logarithmically with distance, whereas changes in the concentrations of Ni, Zn, Cd and phosphate with distance were small. These results suggest that the distributions of Fe and Mn were controlled mainly by input from shelf sediment and removal through scavenging processes. Based on the phase distributions of Fe and Mn, which were calculated as ratios between

  20. Experimental investigation of inhomogeneities, nanoscopic phase separation, and magnetism in arc melted Fe-Cu metals with equal atomic ratio of the constituents

    KAUST Repository

    Hassnain Jaffari, G.

    2015-12-16

    Composition gradient and phase separation at the nanoscale have been investigated for arc-melted and solidified with equiatomic Fe-Cu. Diffraction studies revealed that Fe and Cu exhibited phase separation with no trace of any mixing. Microscopy studies revealed that immiscible Fe-Cu form dense bulk nanocomposite. The spatial distribution of Fe and Cu showed existence of two distinct regions, i.e., Fe-rich and Cu-rich regions. Fe-rich regions have Cu precipitates of various sizes and different shapes, with Fe forming meshes or channels greater than 100 nm in size. On the other hand, the matrix of Cu-rich regions formed strips with fine strands of nanosized Fe. Macromagnetic response of the system showed ferromagnetic behavior with a magnetic moment being equal to about 2.13 μB/Fe atom and a bulk like negligible value of coercivity over the temperature range of 5–300 K. Anisotropy constant has been calculated from various laws of approach to saturation, and its value is extracted to be equal to 1350 J/m3. Inhomogeneous strain within the Cu and Fe crystallites has been calculated for the (unannealed) sample solidified after arc-melting. Annealed sample also exhibited local inhomogeneity with removal of inhomogeneous strain and no appreciable change in magnetic character. However, for the annealed sample phase separated Fe exhibited homogenous strain.

  1. New Constraints on the Abundance of 60Fe in the Early Solar System

    Science.gov (United States)

    Trappitsch, Reto; Boehnke, Patrick; Stephan, Thomas; Telus, Myriam; Savina, Michael R.; Pardo, Olivia; Davis, Andrew M.; Dauphas, Nicolas; Pellin, Michael J.; Huss, Gary R.

    2018-04-01

    Establishing the abundance of the extinct radionuclide 60Fe (half-life 2.62 Ma) in the early solar system is important for understanding the astrophysical context of solar system formation. While bulk measurements of early solar system phases show a low abundance consistent with galactic background, some in situ measurements by secondary ion mass spectrometry (SIMS) imply a higher abundance, which would require injection from a nearby supernova (SN). Here we present in situ nickel isotopic analyses by resonance ionization mass spectrometry (RIMS) in a chondrule from the primitive meteorite Semarkona (LL3.00). The same chondrule had been previously analyzed by SIMS. Despite improved precision compared to SIMS, the RIMS nickel isotopic data do not reveal any resolved excesses of 60Ni that could be unambiguously ascribed to in situ 60Fe decay. Linear regression of 60Ni/58Ni versus 56Fe/58Ni yields an initial 60Fe/56Fe ratio for this chondrule of (3.8 ± 6.9) × 10‑8, which is consistent with both the low initial value found by bulk measurements and the low end of the range of initial ratios inferred from some in situ work. The same regression also gives a solar initial 60Ni/58Ni ratio, which shows that this sample was not disturbed by nickel mobilization, thus agreeing with a low initial 60Fe/56Fe ratio. These findings agree with a re-evaluation of previous SIMS measurements of the same sample. Supernova injection of 60Fe into the solar system or its parental cloud material is therefore not necessary to account for the measured solar system’s initial amount of 60Fe.

  2. First-principle study of single TM atoms X (X=Fe, Ru or Os) doped monolayer WS2 systems

    Science.gov (United States)

    Zhu, Yuan-Yan; Zhang, Jian-Min

    2018-05-01

    We report the structural, magnetic and electronic properties of the pristine and single TM atoms X (X = Fe, Ru or Os) doped monolayer WS2 systems based on first-principle calculations. The results show that the W-S bond shows a stronger covalent bond, but the covalency is obviously weakened after the substitution of W atom with single X atoms, especially for Ru (4d75s1) with the easily lost electronic configuration. The smaller total energies of the doped systems reveal that the spin-polarized states are energetically favorable than the non-spin-polarized states, and the smallest total energy of -373.918 eV shows the spin-polarized state of the Os doped monolayer WS2 system is most stable among three doped systems. In addition, although the pristine monolayer WS2 system is a nonmagnetic-semiconductor with a direct band gap of 1.813 eV, single TM atoms Fe and Ru doped monolayer WS2 systems transfer to magnetic-HM with the total moments Mtot of 1.993 and 1.962 μB , while single TM atom Os doped monolayer WS2 systems changes to magnetic-metal with the total moments Mtot of 1.569 μB . Moreover, the impurity states with a positive spin splitting energies of 0.543, 0.276 and 0.1999 eV near the Fermi level EF are mainly contributed by X-dxy and X-dx2-y2 states hybridized with its nearest-neighbor atom W-dz2 states for Fe, Ru and Os doped monolayer WS2 system, respectively. Finally, we hope that the present study on monolayer WS2 will provide a useful theoretical guideline for exploring low-dimensional spintronic materials in future experiments.

  3. Continuous preparation of Fe3O4 nanoparticles through Impinging Stream-Rotating Packed Bed reactor and their electrochemistry detection toward heavy metal ions

    International Nuclear Information System (INIS)

    Fan, Hong-Lei; Zhou, Shao-Feng; Gao, Jing; Liu, You-Zhi

    2016-01-01

    We reported the continuous preparation and electrochemical behavior toward heavy metal ions of the Fe 3 O 4 nanoparticles (Fe 3 O 4 NPs). This Fe 3 O 4 NPs were fabricated through a novel Impinging Stream-Rotating Packed Bed reactor with a high production rate of 2.23 kg/hour. The as-prepared Fe 3 O 4 NPs were quasi-spherical with a mean diameter of about 10 nm and shown the characteristics of superparamagnetism with the saturated magnetization of 60.5 emu/g. The electrochemical characterization of the as-prepared Fe 3 O 4 NPs toward heavy metal ions were evaluated using square wave anodic stripping voltammetry (SWASV) analysis. The results indicated that the modified electrode could be used to individual detection of Pb(II), Cu(II), Hg(II) and Cd(II). In particular, the modified electrode exhibited the selective detection toward Pb(II) with higher sensitivity of 14.9 μA/μM, while the response to Cu(II), Hg(II) and Cd(II) were negligible. Besides, the modified electrode shown good stability and potential practical applicability in the electrochemical determination of Pb(II). This above results offered a simple method for continuous preparation sensing materials in the application field of electrochemical detection of toxic metal ions through the technology of process intensification. - Highlights: • Fe 3 O 4 nanoparticles were continuous prepared through IS-RPB reactor. • The Fe 3 O 4 nanoparticles showed selective detection of heavy metal ions. • It exhibited favorable sensitivity (14.9 μA μM −1 ) and LOD (0.119 μM) for Pb(II). • The as-prepared nanoparticles showed favorable potential application.

  4. Continuous preparation of Fe{sub 3}O{sub 4} nanoparticles through Impinging Stream-Rotating Packed Bed reactor and their electrochemistry detection toward heavy metal ions

    Energy Technology Data Exchange (ETDEWEB)

    Fan, Hong-Lei [Shanxi Province Key Laboratory of Higee-Oriented Chemical Engineering, North University of China, Taiyuan, 030051 (China); Zhou, Shao-Feng [Shanxi Province Key Laboratory of Functional Nanocomposites, North University of China, Taiyuan, 030051 (China); Gao, Jing [Shanxi Province Key Laboratory of Higee-Oriented Chemical Engineering, North University of China, Taiyuan, 030051 (China); Liu, You-Zhi, E-mail: lyzzhongxin@126.com [Shanxi Province Key Laboratory of Higee-Oriented Chemical Engineering, North University of China, Taiyuan, 030051 (China)

    2016-06-25

    We reported the continuous preparation and electrochemical behavior toward heavy metal ions of the Fe{sub 3}O{sub 4} nanoparticles (Fe{sub 3}O{sub 4} NPs). This Fe{sub 3}O{sub 4} NPs were fabricated through a novel Impinging Stream-Rotating Packed Bed reactor with a high production rate of 2.23 kg/hour. The as-prepared Fe{sub 3}O{sub 4} NPs were quasi-spherical with a mean diameter of about 10 nm and shown the characteristics of superparamagnetism with the saturated magnetization of 60.5 emu/g. The electrochemical characterization of the as-prepared Fe{sub 3}O{sub 4} NPs toward heavy metal ions were evaluated using square wave anodic stripping voltammetry (SWASV) analysis. The results indicated that the modified electrode could be used to individual detection of Pb(II), Cu(II), Hg(II) and Cd(II). In particular, the modified electrode exhibited the selective detection toward Pb(II) with higher sensitivity of 14.9 μA/μM, while the response to Cu(II), Hg(II) and Cd(II) were negligible. Besides, the modified electrode shown good stability and potential practical applicability in the electrochemical determination of Pb(II). This above results offered a simple method for continuous preparation sensing materials in the application field of electrochemical detection of toxic metal ions through the technology of process intensification. - Highlights: • Fe{sub 3}O{sub 4} nanoparticles were continuous prepared through IS-RPB reactor. • The Fe{sub 3}O{sub 4} nanoparticles showed selective detection of heavy metal ions. • It exhibited favorable sensitivity (14.9 μA μM{sup −1}) and LOD (0.119 μM) for Pb(II). • The as-prepared nanoparticles showed favorable potential application.

  5. Electrolytic systems and methods for making metal halides and refining metals

    Science.gov (United States)

    Holland, Justin M.; Cecala, David M.

    2015-05-26

    Disclosed are electrochemical cells and methods for producing a halide of a non-alkali metal and for electrorefining the halide. The systems typically involve an electrochemical cell having a cathode structure configured for dissolving a hydrogen halide that forms the halide into a molten salt of the halogen and an alkali metal. Typically a direct current voltage is applied across the cathode and an anode that is fabricated with the non-alkali metal such that the halide of the non-alkali metal is formed adjacent the anode. Electrorefining cells and methods involve applying a direct current voltage across the anode where the halide of the non-alkali metal is formed and the cathode where the non-alkali metal is electro-deposited. In a representative embodiment the halogen is chlorine, the alkali metal is lithium and the non-alkali metal is uranium.

  6. Study of metal removal by square Wetland System with Eleocharis SP. using SR-XRF

    Energy Technology Data Exchange (ETDEWEB)

    Avelino Neto, Sebastiao; Moreira, Silvana [Universidade Estadual de Campinas (UNICAMP), Campinas, SP (Brazil). Faculdade de Engenharia Civil, Arquitetura e Urbanismo]. E-mails: savneto@bol.com.br; silvana@fec.unicamp.br

    2007-07-01

    The pollution of the water resources for metals, results of different economic activities. The objective of the present study was to use the SR-TXRF technique to evaluate the performance of Wetland system cultivated with Eleocharis sp. installed at FEAGRI-UNICAMP, in the metal removal. The metals analyzed were Cr, Mn, Fe, Zn and Pb. Samples of the wastewater in the exit, Eleocharis sp. leaf and medium boulder were collected during 20 weeks consecutively. The system was operated with different outflows and hydraulic detention times (HDT) as: 600 L.day{sup -1} (HDT 2 days), 400 L.day-1 (HDT 3 days), 300 L.day{sup -1} (HDT 4 days) and 200 L.day{sup -1} (HDT 6 days). The main source of metal removal was medium boulder with efficiency varying 30.1% for Cr and 98.9% for Pb, independent of the hydraulic detention time (HDT) used. The efficiency of the wetland in the Cr removal varied between 39.6 and 98.7%, and for Mn was higher than 81.6%. For Fe the performance was higher than 70.6% and for Cu the efficiency varied between 88.4 and 99.7 %, while for Pb the variation was 67.5 to 98.4 %. The wetland system with Eleocharis sp were in agreement with CONAMA legislation concern to Fe, Cu and Zn removal and for HDT of 2, 3, 4 and 6 days (HDT), moreover for Mn was necessary 4 and 6 days (HDT) and for Cr and Pb 6 days (HDT). (author)

  7. Study of metal removal by square Wetland System with Eleocharis SP. using SR-XRF

    International Nuclear Information System (INIS)

    Avelino Neto, Sebastiao; Moreira, Silvana

    2007-01-01

    The pollution of the water resources for metals, results of different economic activities. The objective of the present study was to use the SR-TXRF technique to evaluate the performance of Wetland system cultivated with Eleocharis sp. installed at FEAGRI-UNICAMP, in the metal removal. The metals analyzed were Cr, Mn, Fe, Zn and Pb. Samples of the wastewater in the exit, Eleocharis sp. leaf and medium boulder were collected during 20 weeks consecutively. The system was operated with different outflows and hydraulic detention times (HDT) as: 600 L.day -1 (HDT 2 days), 400 L.day-1 (HDT 3 days), 300 L.day -1 (HDT 4 days) and 200 L.day -1 (HDT 6 days). The main source of metal removal was medium boulder with efficiency varying 30.1% for Cr and 98.9% for Pb, independent of the hydraulic detention time (HDT) used. The efficiency of the wetland in the Cr removal varied between 39.6 and 98.7%, and for Mn was higher than 81.6%. For Fe the performance was higher than 70.6% and for Cu the efficiency varied between 88.4 and 99.7 %, while for Pb the variation was 67.5 to 98.4 %. The wetland system with Eleocharis sp were in agreement with CONAMA legislation concern to Fe, Cu and Zn removal and for HDT of 2, 3, 4 and 6 days (HDT), moreover for Mn was necessary 4 and 6 days (HDT) and for Cr and Pb 6 days (HDT). (author)

  8. Adsorption and separation of CO{sub 2} on Fe(II)-MOF-74: Effect of the open metal coordination site

    Energy Technology Data Exchange (ETDEWEB)

    Lou, Wolong; Yang, Jiangfeng; Li, Libo; Li, Jinping, E-mail: Jpli211@hotmail.com

    2014-05-01

    We describe the successful synthesis of Fe{sub 2}(dobdc) (dobdc{sup 4−}=2, 5-dioxido-1, 4-benzenedicarboxylate), which has an open metal coordination site Fe(II), and investigate the adsorption properties of three important molecules CO{sub 2}, CH{sub 4} and N{sub 2} on Fe{sub 2}(dobdc) and an oxidized analog, Fe{sub 2}(O{sub 2})(dobdc). We found that CO{sub 2} adsorption isotherm of Fe{sub 2}(dobdc) at 10 bar was very different from Fe{sub 2}(O{sub 2})(dobdc), with the capacities of 144.5 cm{sup 3} g{sup −1} and 98.1 cm{sup 3} g{sup −1}, respectively. The adsorption capacities for CH{sub 4} were 75.8 cm{sup 3} g{sup −1} and 36.8 cm{sup 3} g{sup −1}, respectively, at 10 bar in these materials. Using ideal adsorbed solution theory (IAST), we obtain the adsorption selectivity for CO{sub 2} using equimolar mixtures of CO{sub 2}/CH{sub 4} and CO{sub 2}/N{sub 2} with Fe{sub 2}(dobdc) and Fe{sub 2}(O{sub 2})(dobdc) as a function of pressure. Fe{sub 2}(dobdc) has a higher, more stable separation factor. - Graphical abstract: The selectivity of CO{sub 2}/CH{sub 4} mixture (50%/50%) on Fe{sub 2}(dobdc) and Fe{sub 2}(O{sub 2})(dobdc). - Highlights: • We explored the contrastive adsorption of CO{sub 2}, CH{sub 4}, and N{sub 2} in Fe{sub 2}(dobdc) and Fe{sub 2}(O{sub 2})(dobdc) for the first time. • Through IAST, we obtain the adsorption selectivity for CO{sub 2} from the equimolar mixture of CO{sub 2}/CH{sub 4} and CO{sub 2}/N{sub 2} for Fe{sub 2}(dobdc) and Fe{sub 2}(O{sub 2})(dobdc). • We determined that the open coordination site of Fe(II) is the main reason for different adsorption performances.

  9. [Systemic reactions to orally applied metal alloys].

    Science.gov (United States)

    Feilzer, A J; Kleverlaan, C J; Prahl, C; Muris, J

    2013-06-01

    Orally applied metal alloys can cause undesirable physical effects. A distinction needs to be made in this respect between local and systemic reactions and toxic and immunological reactions. A case is presented which illustrates this problem. In this case, the application of orthodontic appliances was probably the trigger for an exacerbation of nickel allergy. The oral exposure to nickel resulted in hand eczema. The patient was also exposed to nickel by single-unit fixed dental prostheses, a removable dental prosthesis, and food, as a result of which removal of the orthodontic appliances did not result in complete healing. Therefore, the single-unit fixed dental prostheses also had to be removed and food had to be prepared henceforward in nickel free pans.

  10. Molten metal feed system controlled with a traveling magnetic field

    International Nuclear Information System (INIS)

    Praeg, W.F.

    1991-01-01

    This patent describes a continuous metal casting system in which the feed of molten metal controlled by means of a linear induction motor capable of producing a magnetic traveling wave in a duct that connects a reservoir of molten metal to a caster. The linear induction motor produces a traveling magnetic wave in the duct in opposition to the pressure exerted by the head of molten metal in the reservoir

  11. Indentation size effects in the nano- and micro-hardness of a Fe-based bulk metallic glass

    Energy Technology Data Exchange (ETDEWEB)

    Xu, F., E-mail: xufu@xtu.edu.cn; Ding, Y.H.; Deng, X.H.; Zhang, P.; Long, Z.L.

    2014-10-01

    Hardness of a Fe-based bulk metallic glass (BMG) was evaluated by both atomic force microscopy (AFM) nanoindentation (nano-hardness) and instrumented indentation with a traditional indenter setup (micro-hardness) under different maximum loads at room temperature. The nano-hardness and the micro-hardness were found to be comparable. For both of the indentation methods, indentation size effect (ISE) is detected as increase in hardness with decrease in indentation peak load. It is proposed that strain rate dependent softening, loading history and the lag between free volume creation and mechanical softening should be responsible for the ISE in this BMG. Furthermore, ISE is found to be more significant in AFM nanoindentation than in instrumented indentation. This can be explained by taking into account the effect of exerted peak load and the face angle of the indenter in a qualitative manner.

  12. Exchange bias in sputtered FeNi/FeMn systems: Effect of short low-temperature heat treatments

    Energy Technology Data Exchange (ETDEWEB)

    Savin, Peter, E-mail: peter.savin@urfu.ru [Department of Magnetism and Magnetic Nanomaterials, Laboratory of Magnetic Sensors, Ural Federal University, 620002 Ekaterinburg (Russian Federation); Guzmán, Jorge [Instituto de Ciencia de Materiales de Madrid-CSIC, 28049 Madrid (Spain); Lepalovskij, Vladimir [Department of Magnetism and Magnetic Nanomaterials, Laboratory of Magnetic Sensors, Ural Federal University, 620002 Ekaterinburg (Russian Federation); Svalov, Andrey; Kurlyandskaya, Galina [Department of Magnetism and Magnetic Nanomaterials, Laboratory of Magnetic Sensors, Ural Federal University, 620002 Ekaterinburg (Russian Federation); Departamento de Electricidad y Electrónica, Universidad del País Vasco (UPV/EHU), 48940 Leioa, Vizcaya (Spain); Asenjo, Agustina [Instituto de Ciencia de Materiales de Madrid-CSIC, 28049 Madrid (Spain); Vas’kovskiy, Vladimir [Department of Magnetism and Magnetic Nanomaterials, Laboratory of Magnetic Sensors, Ural Federal University, 620002 Ekaterinburg (Russian Federation); Vazquez, Manuel [Department of Magnetism and Magnetic Nanomaterials, Laboratory of Magnetic Sensors, Ural Federal University, 620002 Ekaterinburg (Russian Federation); Instituto de Ciencia de Materiales de Madrid-CSIC, 28049 Madrid (Spain)

    2016-03-15

    Short (5 min) post-deposition thermal treatments under magnetic field at low temperature (up to 200 °C) performed in exchange-coupled FeNi(40 nm)/FeMn(20 nm) bilayer thin films prepared by magnetron sputtering are shown to be effective to significantly modify their exchange field (from around 40 Oe down to 27 Oe) between FeNi and FeMn layers. A similar exchange field decrease was observed for the first deposited FeNi layer of the FeNi(40 nm)/FeMn(20 nm)/FeNi(40 nm) trilayer films after the same thermal treatments. The exchange field value for the second FeNi layer was not substantially changed. The X-ray diffraction patterns indicates that such a heat treatment has no effect on the grain size and crystalline texture of the films, while atomic force microscope studies reveal an increase of the surface roughness after the treatment which is more noticeable in the case of the trilayer film. Analysis of the experimental results leads us to conclude that the variations of the exchange field after heat treatment are likely caused by a modification of interfacial roughness and/or interfacial magnetic structure, but unlikely by the changes in the microstructure and/or changes of composition of the antiferromagnetic FeMn layer. - Highlights: • FeNi/FeMn bilayers and FeNi/FeMn/FeNi trilayers were prepared by magnetron sputtering. • Post-deposition heat treatments at the temperatures below 200 °C during 5 min were made. • Annealing reduces the exchange field for the first FeNi layer in trilayers. • The exchange field value for the second FeNi layer was not substantially changed. • Exchange field changes are most likely caused by a modification of interface roughness.

  13. Metal-Organic Frameworks Triggered High-Efficiency Li storage in Fe-Based Polyhedral Nanorods for Lithium-ion Batteries

    International Nuclear Information System (INIS)

    Shen, Lisha; Song, Huawei; Wang, Chengxin

    2017-01-01

    Recently, metal organic framework (MOF) nanostructures have been frequently reported in the field of energy storage, specifically for Li-ion or Na-ion storage. By inter-separating the active sites of metal cluster and organic ligands, MOF nanostructures are exceptionally promising for realizing fast ion exchange and high-efficiency transportation and addressing the intricate issues that the energy-intensive Li-ion batteries have faced over many years. The related ion-storage mechanism remains to be explored. Is the traditional redox reaction mechanism operative for these nanostructure, as it is for transitional metal oxide? Herein, taking [Fe 3 O(BDC) 3 (H 2 O) 2 (NO 3 )]n (Fe-MIL-88B) as an example, an Fe-based metal organic polyhedral nanorods of MIL–88 B structure was designed as an anode for Li-ion storage. When tested at 60 mA g −1 , the nanoporous Fe-MIL–88 B polyhedral nanorods retained a reversible capacity of 744.5 mAh g −1 for more than 400 cycles. Ex situ characterizations of the post-cycled electrodes revealed that both the transition metal ions and the organic ligands contributed to the high reversible specific capacity. The polyhedral nanorods electrodes held the metal-organic skeleton together throughout the battery operation, although in a somewhat different manner than the pristine ones. This further substantiated that some MOF nanostructures are more appropriate than others for stable lithiation/delithiation processes. State-of-the-art CR2032 full cells showed that a high capacity of 86.8 mAh g −1 that was retained after 100 cycles (herein, the capacity for the full cell was calculated based on both the weight of the anode and the cathode, and the charge-discharge rate was 0.25C), when commercial LiFePO 4 powders were used as the cathode.

  14. Electrical and magnetic properties of Fe-based bulk metallic glass with minor Co and Ni addition

    Energy Technology Data Exchange (ETDEWEB)

    Jung, H.Y. [IFW Dresden, Institute for Complex Materials, D–01069 Dresden (Germany); Stoica, M. [IFW Dresden, Institute for Complex Materials, D–01069 Dresden (Germany); POLITEHNICA University of Timisoara, P-ta Victoriei 2, Timisoara (Romania); Yi, S. [Department of Materials Science and Metallurgical Engineering, Kyungpook National University, 702–701 Daegu (Korea, Republic of); Kim, D.H. [Center for Non-crystalline Materials, Department of Metallurgical Engineering, Yonsei University, 120–749 Seoul (Korea, Republic of); Eckert, J. [IFW Dresden, Institute for Complex Materials, D–01069 Dresden (Germany); University of Technology Dresden, Institute of Materials Science, D–01062 Dresden (Germany)

    2014-09-01

    The effect of minor Co and Ni alloying on soft magnetic properties and electrical resistivity of Fe{sub 75.5}C{sub 7.0}Si{sub 3.3}B{sub 5.5}P{sub 8.7} (at%) bulk metallic glass has been investigated. Within examined compositional range (Co and Ni up to 4 at%, respectively), the saturation magnetization and electrical resistivity of the alloys continuously decrease with increasing Co or Ni content, while the Curie temperature and initial permeability increase. Comparing the effect of Co and Ni additions, the alloys with Co addition have much higher Curie temperature and saturation magnetization than the alloy with Ni addition. Also, the Co-added alloys show smaller coercivity and larger permeability than the Ni-added alloys. The present results suggest that minor addition of Co can provide better effectiveness to enhance the magnetic softness of Fe-based BMGs than minor Ni addition. - Highlights: • Soft magnetic characteristics of CI-based BMGs can be enhanced with minor Co and Ni alloying. • Minor Co addition can provide better effectiveness to enhance the magnetic softness of CI-based BMG than Ni addition. • Optimum Co addition enlarges atomic packing density and randomness of amorphous structure.

  15. THE BEHAVIOR OF SOLUBLE METALS ELUTED FROM Ni/Fe-BASED ALLOY REACTORS AFTER HIGH-TEMPERATURE AND HIGH-PRESSURE WATER PROCESS

    Directory of Open Access Journals (Sweden)

    M. Faisal

    2012-05-01

    Full Text Available The behavior of heavy metals eluted from the wall of Ni/Fe-based alloy reactors after high-temperature and high-pressure water reaction were studied at temperatures ranging from 250 to 400oC. For this purpose, water and cysteic acid were heated in two reactor materials which are SUS 316 and Inconel 625. Under the tested conditions, the erratic behaviors of soluble metals eluted from the wall of Ni/Fe-based alloy in high temperature water were observed. Results showed that metals could be eluted even at a short contact time. The presence of air also promotes elution at sub-critical conditions. At sub-critical conditions, a significant amount of Cr was extracted from SUS 316, while only traces of Ni, Fe, Mo and Mn were eluted. In contrast, Ni was removed in significant amounts compared to Cr when Inconel 625 was tested. It was observed that eluted metals tend to increased under acidic conditions and most of those metals were over the limit of WHO guideline for drinking water. The results are significant both on the viewpoint of environmental regulation on disposal of wastes containing heavy metals, toxicity of resulting product and catalytic effect on a particular reaction.

  16. Phase Equilibria and Magnetic Phases in the Ce-Fe-Co-B System

    Directory of Open Access Journals (Sweden)

    Tian Wang

    2016-12-01

    Full Text Available Ce-Fe-Co-B is a promising system for permanent magnets. A high-throughput screening method combining diffusion couples, key alloys, Scanning Electron Microscope/Wavelength Dispersive X-ray Spectroscope (SEM/WDS, and Magnetic Force Microscope (MFM is used in this research to understand the phase equilibria and to explore promising magnetic phases in this system. Three magnetic phases were detected and their homogeneity ranges were determined at 900 °C, which were presented by the formulae: Ce2Fe14−xCoxB (0 ≤ x ≤ 4.76, CeCo4−xFexB (0 ≤ x ≤ 3.18, and Ce3Co11−x FexB4 (0 ≤ x ≤ 6.66. The phase relations among the magnetic phases in this system have been studied. Ce2(Fe, Co14B appears to have stronger magnetization than Ce(Co, Fe4B and Ce3(Co, Fe11B4 from MFM analysis when comparing the magnetic interactions of selected key alloys. Also, a non-magnetic CeCo12−xFexB6 (0 ≤ x ≤ 8.74 phase was detected in this system. A boron-rich solid solution with Ce13FexCoyB45 (32 ≤ x ≤ 39, 3 ≤ y ≤ 10 chemical composition was also observed. However, the crystal structure of this phase could not be found in the literature. Moreover, ternary solid solutions ε1 (Ce2Fe17−xCox (0 ≤ x ≤ 12.35 and ε2 (Ce2Co17−xFex (0 ≤ x ≤ 3.57 were found to form between Ce2Fe17 and Ce2Co17 in the Ce-Fe-Co ternary system at 900 °C.

  17. Effects of Fe, Ni, and Fe/Ni metallic nanoparticles on power production and biosurfactant production from used vegetable oil in the anode chamber of a microbial fuel cell.

    Science.gov (United States)

    Liu, Jia; Vipulanandan, Cumaraswamy

    2017-08-01

    In this study, metallic nanoparticles (Fe, Ni, and Fe/Ni) were used as cathode catalysts to enhance power production and to improve the anode performance of a two-chambered microbial fuel cell (MFC). The metallic nanoparticles were rod-shaped and produced by the precipitation/co-precipitation method. A biosurfactant was produced in the anode chamber of the MFC from used vegetable oil by the bacteria Serratia sp. Overall cell voltage, power density, bacterial growth, and biosurfactant production were studied by applying different types of metallic nanoparticles to the cathode electrode. The influence of various types of nanoparticles on the impedance of the MFC was also investigated by electrochemical impedance spectroscopy (EIS), including analyses of anode impedance, cathode impedance, anode solution resistance, cathode solution resistance, and membrane resistance. The nanoparticles improved MFC performance in the following order: Fe>Ni>Fe/Ni. The addition of 1.5mg/cm 2 Fe nanoparticles to the cathode surface enhanced power production by over 500% to 66.4mW/m 3 , promoted bacterial growth and biosurfactant production in the anode solution by 132.5% and 32.0%, respectively, and reduced anode impedance, cathode impedance, and membrane resistance by 26.8%, 81.6%, and 33.8% to 159.00Ω, 7.69Ω, and 261.09Ω, respectively. For the first time, biosurfacant production in the anode chamber of the MFC was promoted by using the metallic nanoparticles as cathode catalysts. By improving the cathode properties, this study showed a new way to manipulated the performance of the anode chamber of the MFC. Copyright © 2017 Elsevier Ltd. All rights reserved.

  18. Compositions of corrosion-resistant Fe-based amorphous metals suitable for producing thermal spray coatings

    Science.gov (United States)

    Farmer, Joseph C; Wong, Frank M.G.; Haslam, Jeffery J; Ji, Xiaoyan; Day, Sumner D; Blue, Craig A; Rivard, John D.K.; Aprigliano, Louis F; Kohler, Leslie K; Bayles, Robert; Lemieux, Edward J; Yang, Nancy; Perepezko, John H; Kaufman, Larry; Heuer, Arthur; Lavernia, Enrique J

    2013-09-03

    A method of coating a surface comprising providing a source of amorphous metal that contains manganese (1 to 3 atomic %), yttrium (0.1 to 10 atomic %), and silicon (0.3 to 3.1 atomic %) in the range of composition given in parentheses; and that contains the following elements in the specified range of composition given in parentheses: chromium (15 to 20 atomic %), molybdenum (2 to 15 atomic %), tungsten (1 to 3 atomic %), boron (5 to 16 atomic %), carbon (3 to 16 atomic %), and the balance iron; and applying said amorphous metal to the surface by a spray.

  19. Formation and magnetic properties of InFeP:Ag nano-rods fabricated with noble metal Ag using ion milling method.

    Science.gov (United States)

    Sohn, Jae Min; Kim, Hyungsang; Im, Hyunsik; Kim, Hyungbae; Lee, Juwon; Shon, Yoon; Subramaniam, Ganapathi; Kang, Tae Won; Kim, Deuk Young; Koo, Hyun Cheol; Lee, Joo-Hyeon; Song, Jin Dong; Park, Chang-Soo; Kim, Eun Kyu

    2017-11-03

    The formation including density, and height of InFeP:Ag nano-rods doped with noble metal Ag using ion milling method was preponderantly determined from TEM and XRD analyses. We investigate especially the enhanced ferromagnetism of the well aligned InFeP:Ag nano-rods. AES and XPS measurements were carried out in order to investigate the incorporation of Ag and to verify the local chemical bonding of InFeP:Ag nano-rods. The variation of FWHM for DCRC and TAD peaks demonstrates that noble metal Ag is incorporated into InFeP:Ag nano-rods. The noticeable ferromagnetic signature (M-H curve) of the InFeP:Ag nano-rods is observed and Tc persists up to near 350 K (3.9 × 10-4 emu/g) from temperature - dependence magnetization (M-T curve) measurements. This study suggests that the InFeP:Ag nano-rods should be a potential candidate for the application of spintronic devices. © 2017 IOP Publishing Ltd.

  20. Determination of transition metal ion distribution in cubic spinel Co1.5Fe1.5O4 using anomalous x-ray diffraction

    Directory of Open Access Journals (Sweden)

    M. N. Singh

    2015-08-01

    Full Text Available We report anomalous x-ray diffraction studies on Co ferrite with composition Co1.5Fe1.5O4 to obtain the distribution of transition metal ions in tetrahedral and octahedral sites. We synthesize spinel oxide (Co1.5Fe1.5O4 through co-precipitation and subsequent annealing route. The imaginary part (absorption of the energy dependent anomalous form factor is measured and the real part is calculated theoretically through Kramers–Krönig transformation to analyze anomalous x-ray diffraction peak intensities. Fe and Co K-edge x-ray absorption near edge structure (XANES spectra are used to estimate charge states of transition metals. Our analysis, within experimental errors, suggests 44% of the tetrahedral sites contain Co in +2 oxidation state and the rest 56% sites contain Fe in +2 and +3 oxidation states. Similarly, 47% of the octahedral sites contain Fe in +3 oxidation states, whereas, the rest of the sites contain Co in +2 and +3 oxidation states. While a distinct pre-edge feature in the Fe K-edge XANES is observed, Co pre-edge remains featureless. Implications of these results to magnetism are briefly discussed.

  1. A critical review on the process of contaminant removal in Fe0-H2O systems.

    Science.gov (United States)

    Noubactep, C

    2008-08-01

    A central aspect of the contaminant removal by elemental iron materials (Fe0 or Fe0 materials) is that reduction reactions are mediated by the iron surface (direct reduction). This premise was introduced by the pioneers of the reactive wall technology and is widely accepted by the scientific community. In the meantime enough evidence has been provided to suggest that contaminant reduction through primary corrosion products (secondary reductants) does indeed occur (indirect reduction). It was shown for decades that iron corrosion in the pH range of natural waters (4-9) inevitably yields an obstructive oxide film of corrosion products at the metal surface (oxide film). Therefore, contaminant adsorption on to corrosion products and contaminant co-precipitation with corrosion products inevitably occurs. For adsorbed and coprecipitated contaminants to be directly reduced the oxide film should be electronic conductive. This study argues through a literature review a series of points which ultimately lead to the conclusion that, if any quantitative contaminant reduction occurs in the presence of Fe0 materials, it takes place within the matrix of corrosion products and is not necessarily a direct reduction. It is concluded that Fe0 materials act both as source of corrosion products for contaminant adsorption/coprecipitation and as a generator of FeII and H2 (H) for possible catalytic contaminant reduction.

  2. Removal of Heavy Metals Pb2+, Cu2+, Zn2+, Cd2+, Ni2+, Co2+ and Fe3+ from Aqueous Solutions by using Xanthium Pensylvanicum

    Directory of Open Access Journals (Sweden)

    Jaber SALEHZADEH

    2013-11-01

    Full Text Available The hazardous ill effects of heavy metals on the environment and public health is a matter of serious concern. Biosorption is emerging as a sustainable effective technology. Heavy metals in water resources are one of the most important environmental problems of countries. The intensification of industrial activity and environmental stress greatly contributes to the significant rise of heavy metal pollution in water resources making threats on terrestrial and aquatic life. The toxicity of metal pollution is slow and interminable, as these metal ions are non bio-degradable. The adsorption capacity of Xanthium Pensylvanicum towards metal ions such as Pb2+, Cu2+, Zn2+, Cd2+, Ni2+, Co2+ and Fe3+, was studied. The adsorption capacity was performed by batch experiments as a function of process parameters (such as sorption time and pH. Experimental results showed that the removal percentages increasing of metal ions at pH=4, initial concentration of metal ions 10 mg/L, and after 90 min of shaking was: Zn2+ < Cd2+ < Cu2+ < Pb2+ < Ni2+ < Fe3+ < Co2+.

  3. Seasonal variation of major elements (Ca, Mg) and trace metals (Fe, Cu, Zn, Mn) and cultured mussel Perna viridis L. and seawater in the Dona Paula Bay, Goa

    Digital Repository Service at National Institute of Oceanography (India)

    Rivonker, C.U.; Parulekar, A.H.

    The major elements and trace metals were analysed from nussel tissue and the seawater taken from three depths (0, 5 and 9 meters) from the culture site. Range of variation in Ca, Mg, Fe, Cu, Zn and Mn were 226-399; 708-1329; 0.005-0.084; BDL-0...

  4. Photocurrent increase by metal modification of Fe{sub 2}O{sub 3} photoanodes and its effect on photoelectrocatalytic hydrogen production by degradation of organic substances

    Energy Technology Data Exchange (ETDEWEB)

    Iervolino, Giuseppina [Department of Industrial Engineering, University of Salerno, Via Giovanni Paolo II, 132, Fisciano, Salerno, Italy, (Italy); Tantis, Iosif [Department of Chemical Engineering, University of Patras, 26500, Patras (Greece); Sygellou, Lamprini [FORTH/ICE-HT, P.O. Box 1414, 26504, Patras (Greece); Vaiano, Vincenzo, E-mail: vvaiano@unisa.it [Department of Industrial Engineering, University of Salerno, Via Giovanni Paolo II, 132, Fisciano, Salerno, Italy, (Italy); Sannino, Diana [Department of Industrial Engineering, University of Salerno, Via Giovanni Paolo II, 132, Fisciano, Salerno, Italy, (Italy); Lianos, Panagiotis, E-mail: lianos@upatras.gr [Department of Chemical Engineering, University of Patras, 26500, Patras (Greece)

    2017-04-01

    Highlights: • Metals-modified hematite photoanodes prepared by electrodeposition method. • Ti and Ni-modified hematite thin films showed the higher photocurrents values. • The optimal loading of modifier was found at nominal 1% for Ni and 3% for Ti. • The highest H2 production was obtained on 3%Ti-Fe2O3 in the presence of glucose. - Abstract: The present work reports the investigation of photocurrent increase by metal modification of Fe{sub 2}O{sub 3} photoanodes and its effect on photoelectrocatalytic hydrogen production using aqueous solutions containing various organic compounds. Fe{sub 2}O{sub 3} photoanodes were prepared by the electrodeposition method. The efficiency of various metal modifiers of the hematite structure (Ti, Ni, Sn, Co and Cu) has been tested by monitoring the photoelectrochemical behavior of the ensuing photoanodes. Hydrogen production was monitored in an H-shaped reactor using pure and metal-modified hematite films deposited on FTO electrodes as photocatalyst while a combination of commercial carbon paste with dispersed Pt nanoparticles was used as electrocatalyst. In all cases, hydrogen production was obtained by application of a small external electric bias (in the range 0.5- 0.7 V vs Ag/AgCl electrode). Highest photocurrent production has been achieved with a Ti-modified Fe{sub 2}O{sub 3} photoanode in the presence of glucose as sacrificial agent.

  5. Metallurgical study and phase diagram calculations of the Zr-Nb-Fe-(Sn,O) system

    International Nuclear Information System (INIS)

    Toffolon, C.

    2000-01-01

    The Framatome M5 TM Zr-Nb-O alloy with small amounts of Fe is of interest for nuclear applications (PWR fuel cladding).The behaviour of this kind of alloy for in-service conditions strongly depends on the microstructure. Therefore, a metallurgical study of alloys of the Zr-Nb-Fe-(O-Sn) system has been developed in order to study the influence of chemical composition variabilities of Nb, Fe and O and thermal treatments on the resultant microstructure. In order to get some insight on the physical metallurgy of Zr-Nb-Fe-(Sn,O) alloys and to minimize the experiments, it is useful to build a thermodynamic database. With this object, it was necessary to re-optimize and to calculate the low order binary systems such as Fe-Nb and Nb-Sn in order to assess the Zr-Nb-Fe-(Sn,O) system. Then, the experimental studies concerned: the influence of small variations in Nb and O contents on the α/β transus temperatures. A comparison between experimental results and thermodynamic predictions showed a good agreement; the precipitation kinetics of βNb and intermetallic phases in the α phase domain. These experiments showed that the kinetics depends on the initial metallurgical conditions; the determination of the crystallographic structure and the stoichiometry of the ternary Zr-Nb-Fe intermetallic compounds as a function of the temperature. Finally, these experimental data were used to propose a first assessment of the Zr-Nb-Fe(O∼1200 ppm) system. (author)

  6. Topotactic Metal-Insulator Transition in Epitaxial SrFeO x Thin Films

    International Nuclear Information System (INIS)

    Khare, Amit; Shin, Dongwon; Yoo, Tae Sup; Kim, Minu; Kang, Tae Dong

    2017-01-01

    Multivalent transition metal oxides provide fascinating and rich physics related to oxygen stoichiometry. In particular, the adoptability of various valence states of transition metals enables perovskite oxides to display mixed (oxygen) ionic and electronic conduction and catalytic activity useful in many practical applications, including solid-oxide fuel cells (SOFCs), rechargeable batteries, gas sensors, and memristive devices. For proper realization of the ionic conduction and catalytic activity, it is essential to understand the reversible oxidation and reduction process, which is governed by oxygen storage/release steps in oxides. Topotactic phase transformation facilitates the redox process in perovskites with specific oxygen vacancy ordering by largely varying the oxygen concentration of a material without losing the lattice framework. The concentration and diffusion of oxide ions (O 2– ), the valence state of the transition metal cations, and the thermodynamic structural integrity together provide fundamental understanding and ways to explicitly control the redox reaction.[6] In addition, it offers an attractive route for tuning the emergent physical properties of transition metal oxides, via strong coupling between the crystal lattice and electronic structure.

  7. Analysis of thermal expansivity of iron (Fe) metal at ultra high ...

    Indian Academy of Sciences (India)

    structure are unlikely to be successful for predicting the high temperature properties of transition metals due to the complicated many-body nature of the interactions. Wasserman et al [3] have recently studied the thermal properties of iron at high pressures and temperatures within the framework of shell model [7,8], which is ...

  8. Metallothionein Induction as Indicator of Low Level Metal Exposure to Aquatic Macroinvertebrates from a Relatively Unimpacted River System in South Africa.

    Science.gov (United States)

    Kemp, M; Wepener, V; de Kock, K N; Wolmarans, C T

    2017-12-01

    The Marico River is relatively unaffected by anthropogenic activities. However, metal concentrations-mainly from natural sources-occasionally exceed environmental quality guidelines. Macroinvertebrates are capable to react to these metals through processes such as the induction of metallothioneins (MTs). The aims of this study were to determine whether the induction of MTs can be used as indicator of natural metal exposure in not anthropogenically impacted systems and whether there are relationships between metal concentrations in water, sediment and macroinvertebrates and concomitant MT levels. Positive correlations were found between metals in sediment and macroinvertebrates, while there were no correlations between metal concentrations in water and macroinvertebrates. Even in a not anthropogenically impacted system, a positive correlation existed between trace metal bioaccumulation (e.g. Ni, Pb, Zn) in macroinvertebrates and the induction of MTs. There were, however, no correlations between MTs and bioaccumulation of earth metals (e.g. Al, Fe, Mn, Ti).

  9. FeNbB bulk metallic glass: the influence of fluxing technique

    Energy Technology Data Exchange (ETDEWEB)

    Stoica, Mihai; Eckert, Juergen [IFW Dresden, Institute for Complex Materials, P.O. Box 270116, D-01171 Dresden (Germany); Kumar, Santosh [IFW Dresden, Institute for Complex Materials, P.O. Box 270116, D-01171 Dresden (Germany); Materials Science Centre, Indian Institute of Technology, Kharagpur 721302 (India); Roth, Stefan [IFW Dresden, Institute for Metallic Materials, P.O. Box 270116, D-01171 Dresden (Germany); Ram, Shanker [Materials Science Centre, Indian Institute of Technology, Kharagpur 721302 (India); Yavari, Alain Reza [LTPCM-CNRS, Institut National Politechnique de Grenoble, 1130 Rue de la Piscine, BP 75, Saint Martin d' Heres Campus 38402 (France)

    2008-07-01

    Recently, a new Fe-based BMG containing only 3 elements and a very high boron (Fe{sub 66}Nb{sub 4}B{sub 30}) content was synthesized. The preparation of this BMG was done by employing the copper mould casting method and using the fluxing technique. This new BMG is ferromagnetic, with a Curie temperature around 550 K and a saturation magnetization of 105 emu/g. Differential scanning calorimetry (DSC) investigations revealed a reduced glass transition temperature of 0.58 and an extension of the supercooled liquid region of about 31 K, values which indicate a relatively good thermal stability. Fluxed and not-fluxed master alloys were used to cast samples. The present work aims to discuss, for both kinds of samples, the kinetics of the phase formation using the Kissinger analysis and Johnson-Mehl-Avrami plots, correlated with the results obtained from X-ray diffraction (XRD) of samples with different metastable structures. Additionally, the magnetic behaviour of different phase(s) is discussed.

  10. MAS NMR Study of the Metastable Solid Solutions Found in the LiFePO4/FePO4 System

    Energy Technology Data Exchange (ETDEWEB)

    Cabana, Jordi; Shirakawa, Junichi; Chen, Guoying; Richardson, Thomas; Grey, Clare P.

    2009-10-09

    Li and 3IP NMR experiments were conducted on a series of single- or two-phase samples in the LiFePCvFePCM system with different overall lithium contents, and containing the two end-members and/or two metastable solid solution hases, Lio.6FeP04 or Lio.34FeP04. These experiments were carried out at different temperatures in order to search for vacancy/charge ordering and ion/electron mobility in the metastable phases. Evidence for Li+-Fe2+ interactions was bserved for both Lio.6FeP04 and Lio.34FePC>4. The strength of this interaction leads to the formation of LiFePCvlike clusters in the latter, as shown by the room temperature data. Different motional processes are proposed to exist as the temperature is increased and various scenarios are discussed. While concerted lithium-electron hopping and/or correlations explains the data below 125C, evidence for some uncorrelated motion is found at higher temperatures, together with the onset of phase mixing.

  11. Irreversible effects in the FeTi/H system

    International Nuclear Information System (INIS)

    Reilly, J.J.; Johnson, J.R.; Lynch, J.F.; Reidinger, F.

    1982-03-01

    The equilibrium hydrogen absorption isotherm using annealed, strain-free FeTi, exhibits only one plateau up to a composition of FeTiH/sub 1.95/. However, the desorption isotherm, determined immediately after the first hydriding step, exhibits the usual two plateaux. X-ray diffraction results of samples with compositions within the absorption plateau limits indicate the major phases present to be α and γ, although a small amount of β phase was always detected. Apparently the absorption isotherm represents the direct conversion of α → γ and β phase precipitation is almost completely suppressed. Thermodynamic quantities for this conversion are given. The results are attributed to the influence of lattice strain upon the behavior of the β1 and β2 phases. A practical consequence of the effect is the distortion of the pressure-composition isotherm in the β-γ region as a function of hydriding-dehydriding cycles. This is caused by an increase in H solubility of the β and γ phases and the widening of the phase composition limits as the strain increases with cycle number. However, after many hundreds of cycles there is no further significant increase in strain and the isotherm shape becomes essentially fixed and reproducible. The distortion is reversible by mild annealing

  12. Separation of Non-metallic Inclusions from a Fe-Al-O Melt Using a Super-Gravity Field

    Science.gov (United States)

    Song, Gaoyang; Song, Bo; Guo, Zhancheng; Yang, Yuhou; Song, Mingming

    2018-02-01

    An innovative method for separating non-metallic inclusions from a high temperature melt using super gravity was systematically investigated. To explore the separation behavior of inclusion particles with densities less than that of metal liquid under a super-gravity field, a Fe-Al-O melt containing Al2O3 particles was treated with different gravity coefficients. Al2O3 particles migrated rapidly towards the reverse direction of the super gravity and gathered in the upper region of the sample. It was hard to find any inclusion particles with sizes greater than 2 μm in the middle and bottom areas. Additionally, the oxygen content in the middle region of the sample could be reduced to 0.0022 mass pct and the maximum removal rate of the oxygen content reached 61.4 pct. The convection in the melt along the direction of the super gravity was not generated by the super-gravity field, and the fluid velocity in the molten melt consisted only of the rotating tangential velocity. Moreover, the motion behavior of the Al2O3 particles was approximatively determined by Stokes' law along the direction of super gravity.

  13. Metal (Fe, Co, Ni) supported on different aluminas as Fischer-Tropsch catalyst

    Energy Technology Data Exchange (ETDEWEB)

    Dahlan [Chemistry Education Study Program, Universitas Halu Oleo, Jl. HEA Mokodompit, Kendari 93232 (Indonesia); Marsih, I. Nyoman, E-mail: nyoman@chem.itb.ac.id; Ismunandar [Inorganic and Physical Chemistry Division, Departement of Chemistry, Institut Teknologi Bandung, Jl. Ganesha 10, Bandung 40132 (Indonesia); Makertihartha, I. G. B. N. [Department of Chemical Engineering, Institut Teknologi Bandung, Jl. Ganesha 10, Bandung 40132 (Indonesia); Praserthdam, Piyasan; Panpranot, Joongjai [Center of Excellence on Catalysis and Catalytic Reaction Engineering, Department of Chemical Engineering, Chulalongkorn University, 254 Phayathai Road, Bangkok 10330 (Thailand)

    2015-09-30

    This research aimed to compare the physico-chemical properties of the same metal M (M = iron, cobalt, nickel) supported on aluminas with different morphology and pore size as Fischer-Tropsch catalyst. The aluminas applied as support were alumina synthesized through hydrothermal process, alumina formed by pretreatment of catapal and commercial alumina which named as Ahy, Aca, and Aco respectively. Ahy has uniform morphology of nanotubes while Aca and Aco showed non-uniform morphology of particle lumps. The particle lumps of Aca were larger than those of Aco. Ahy, Aca, and Aco respectively has average pore diameter of 2.75, 2.86 and 2.9 nm. Metals were deposited on the supports by incipient-wetness impregnation method. The catalysts were characterized by XRD, H{sub 2}-TPR, and H{sub 2} chemisorption. Catalyst acitivity test for Fischer-Tropsch reaction was carried out in a micro reactor at 200 °C and 1 atm, and molar ratio of H{sub 2}/CO = 2:1. The metal oxide particle size increased in the order M/Aco < M/Aca < M/Ahy. The catalysts reducibility also increased according to the order M/Aco < M/Aca < M/Ahy suggesting that the larger metal oxide particles are more reducible. The number of active site was not proportional to the reducibility because during the reduction, larger metal oxide particles were converted into larger metal particles. On the other hand, the number of active sites was inversely proportional to the particle sizes. The number of active site increased in the order M/Ahy < M/Aco < M/Aca. The catalytic activity also increased in the following order M/Ahy < M/Aco < M/Aca. The activity per active site increased according to the order M/Aca < M/Aco < M/Ahy meaning that for M/Ahy, a little increase in active site will lead to a significance increase in catalytic activity. It showed that Ahy has potential for the better support.

  14. System and process for aluminization of metal-containing substrates

    Energy Technology Data Exchange (ETDEWEB)

    Chou, Yeong-Shyung; Stevenson, Jeffry W.

    2017-12-12

    A system and method are detailed for aluminizing surfaces of metallic substrates, parts, and components with a protective alumina layer in-situ. Aluminum (Al) foil sandwiched between the metallic components and a refractory material when heated in an oxidizing gas under a compression load at a selected temperature forms the protective alumina coating on the surface of the metallic components. The alumina coating minimizes evaporation of volatile metals from the metallic substrates, parts, and components in assembled devices that can degrade performance during operation at high temperature.

  15. Preparation and characterization of Fe-based bulk metallic glasses in plate form

    International Nuclear Information System (INIS)

    Lavorato, G.C.; Fiore, G.; Castellero, A.; Baricco, M.; Moya, J.A.

    2012-01-01

    Amorphous alloys with composition (at%) Fe 48 Cr 15 Mo 14 C 15 B 6 Gd 2 (alloy A) and Fe 48 Cr 15 Mo 14 C 15 B 6 Y 2 (alloy B) were prepared either using pure elements (A and B1) and a commercial AISI430 steel as a base material (B2). When prepared from pure elements both alloys (A and B1) could be cast in plate form with a fixed thickness of 2 mm and variable lengths between 10 and 20 mm by means of copper-mold injection in air atmosphere. In the case of alloy B2, prepared using commercial grade raw materials, rods of 2 mm diameter were obtained. X-ray diffraction and scanning electron microscopy observations confirmed that an amorphous structure was obtained in all the as-cast samples. A minor fraction of crystalline phases (oxides and carbides) was detected on the as-cast surface. Differential scanning calorimetry measurements showed a glass transition temperature at 856 K for alloy A and 841 K for alloy B1, and an onset crystallization temperature of 887 K for alloy A and 885 K for alloy B1. In the case of alloy B2 a slightly different crystallization sequence was observed. Values of hardness (∼13 GPa) and the Young modulus (∼180 GPa) were measured by nanoindentation for both the alloys. The effects of adverse casting conditions (such as air atmosphere, non-conventional injection copper mold casting and partial replacement of pure elements with commercial grade raw materials) on the glass formation and properties of the alloy are discussed.

  16. Preparation and characterization of Fe-based bulk metallic glasses in plate form

    Energy Technology Data Exchange (ETDEWEB)

    Lavorato, G.C. [INTECIN (FIUBA-CONICET), Paseo Colon 850, Capital Federal (Argentina); Dipartimento di Chimica IFM and NIS, Universita di Torino, Torino (Italy); Fiore, G.; Castellero, A.; Baricco, M. [Dipartimento di Chimica IFM and NIS, Universita di Torino, Torino (Italy); Moya, J.A., E-mail: jmoya.fi.uba@gmail.com [IESIING, Facultad de Ingenieria e Informatica, UCASAL, Salta (Argentina); CONICET (Argentina)

    2012-08-15

    Amorphous alloys with composition (at%) Fe{sub 48}Cr{sub 15}Mo{sub 14}C{sub 15}B{sub 6}Gd{sub 2} (alloy A) and Fe{sub 48}Cr{sub 15}Mo{sub 14}C{sub 15}B{sub 6}Y{sub 2} (alloy B) were prepared either using pure elements (A and B1) and a commercial AISI430 steel as a base material (B2). When prepared from pure elements both alloys (A and B1) could be cast in plate form with a fixed thickness of 2 mm and variable lengths between 10 and 20 mm by means of copper-mold injection in air atmosphere. In the case of alloy B2, prepared using commercial grade raw materials, rods of 2 mm diameter were obtained. X-ray diffraction and scanning electron microscopy observations confirmed that an amorphous structure was obtained in all the as-cast samples. A minor fraction of crystalline phases (oxides and carbides) was detected on the as-cast surface. Differential scanning calorimetry measurements showed a glass transition temperature at 856 K for alloy A and 841 K for alloy B1, and an onset crystallization temperature of 887 K for alloy A and 885 K for alloy B1. In the case of alloy B2 a slightly different crystallization sequence was observed. Values of hardness ({approx}13 GPa) and the Young modulus ({approx}180 GPa) were measured by nanoindentation for both the alloys. The effects of adverse casting conditions (such as air atmosphere, non-conventional injection copper mold casting and partial replacement of pure elements with commercial grade raw materials) on the glass formation and properties of the alloy are discussed.

  17. Addressing aquatic hazard classification for metals, metal compounds and alloys in marine systems.

    Science.gov (United States)

    Huntsman-Mapila, P; Skeaff, J M; Pawlak, M; Beaudoin, R

    2016-08-15

    New International Maritime Organization regulations require shippers to classify all solid bulk cargo to indicate whether they are Harmful to the Marine Environment (HME). The objective of this work was to adapt the freshwater Transformation/Dissolution Protocol (T/DP) to marine water to provide a method to determine, when compared with marine Ecotoxicity Reference Values (ERVs), whether a metal-bearing substance is HME. The substances examined were: Cu2O powder; Ni metal powder; Co3O4 powder; and a Ni-Co-Fe alloy, as wire cuttings, which were the same substances examined in the freshwater T/D validation study and afforded comparisons of the reactivity, or measure of the rate and extent of metal release from the metal-bearing substances in freshwater versus marine conditions. The marine T/D method is suitable for conducting examinations of metal-bearing substances with a wide range of reactivities, from the relatively reactive Cu2O powder and the alloy to the Co3O4 powder, which was the least reactive. Crown Copyright © 2016. Published by Elsevier Ltd. All rights reserved.

  18. A guide for validation of FE-Simulations in bulk metal forming

    International Nuclear Information System (INIS)

    Tekkaya, A. Erman

    2005-01-01

    Numerical analysis of metal forming processes is an everyday practice in industry. Forming loads, material flow, forming defects such as underfills, laps and even cracks, stresses in dies and punches, as well as product properties like new hardness distribution, dimensional accuracies and residual stresses are predicted by numerical analysis and used for technology generation. Most of the numerical analysis is done by the finite element method made available for engineers and technicians by numerous by powerful commercial software packages. These software packages act as black-boxes and usually hide the complicated numerical procedures and even their crucial parameters from the applier. Therefore, the question arises during the industrial applications: how accurate is the simulation and how can the results can be assessed? The aim of this paper is to provide a guideline to assess the results of metal forming simulations. Although some ideas are valid for any metal forming process, bulk forming is the process concern. The paper will address firstly the possible sources of error in a finite element analysis of bulk forming processes. Then, some useful elementary knowledge will be summarized. Various levels of validation such as result and ability validation and assessment will be discussed. Finally, interpretation of results will be treated. In this content also some suggestions will be given. (author)

  19. Thermodynamic analysis of Mo(VI)-Fe(III)-S(VI)-H2O system for separation of molybdenum and iron

    Science.gov (United States)

    Xiao, Chao; Zeng, Li; Xiao, Liansheng; Zhang, Guiqing

    2017-11-01

    The separation of molybdenum and iron is one of key issues of the hydrometallurgical preparation of pure molybdenum chemical products. The thermodynamic equilibrium diagrams for distribution of species at different pH values and different concentrations of molybdenum, iron and sulfur with the systems of Mo(VI)-H2O, Fe(III)-S(VI)-H2O and Mo(VI)-Fe(III)-S(VI)-H2O at 298 K were established, separately. Thermodynamic analysis results revealed that both molybdenum and iron were transformed from their anions to cations with the decrease in pH values. The pHMf0.5 for the conversion of molybdenum anions to cations decreased from 0.92 to 0.20 with the increase in the molybdenum concentration from 0.05 mol/L to 1 mol/L (pHMf50 is defined as the pH value when target metal anions occupy 50% mole fraction of total). The total sulfur concentration has significant effect on the conversion of iron (III) species with the pH change. The separation of molybdenum (VI) and iron (III) from acidic solutions using a tertiary amine extractant N235 could be achieved by decreasing the total sulfur concentration and controlling the equilibrium pH in an optimum range. The verification test results showed that the operating window for the separation of Mo(VI) and Fe(III) from a solution containing 0.01 mol/L [Mo]T, 0.05 mol/L [Fe]T and 1.15 mol/L [S]T was in the pH range of 0.5-1.0, which was consistent with the thermodynamic analysis.

  20. Evaluation of the heavy metals Cr, Mn, Fe, Cu, Zn and Pb in water penny wort (Hydrocotyle ranunculoides) from the upper course of the Lerma River, Mexico

    International Nuclear Information System (INIS)

    Zarazua, G.; Avila P, P.; Tejeda, S.; Valdivia B, M.; Macedo M, G.; Zepeda G, C.

    2013-01-01

    The Lerma river is one of the most polluted water bodies in Mexico, it presents low biodiversity and lets grow up aquatic plants resistant to the pollution. The aim of this work was to evaluate the concentration and bioaccumulation factors of Cr, Mn, Fe, Cu, Zn and Pb in aerial and submerged structures of water penny wort (Hydrocotyle ranunculoides) from the upper course of the Lerma river. Inductively coupled plasma-optical emission spectrometry was used to determine the concentration of heavy metals in water and H. ranunculoides. Results show that the bioaccumulation factors of Fe and Zn were higher than those of Cu, Mn, Cr and Pb; with the exception of Zn, bioaccumulation factors were higher in the submerged structures of the plant, which shows low mobility of analyzed metals. As a result of this study H. ranunculoides can be considered as good indicator of metal pollution in water bodies. (Author)

  1. Melting Penetration Simulation of Fe-U System at High Temperature Using MPS-LER

    International Nuclear Information System (INIS)

    Mustari, A P A; Irwanto, Dwi; Yamaji, A

    2016-01-01

    Melting penetration information of Fe-U system is necessary for simulating the molten core behavior during severe accident in nuclear power plants. For Fe-U system, the information is mainly obtained from experiment, i.e. TREAT experiment. However, there is no reported data on SS304 at temperature above 1350°C. The MPS-LER has been developed and validated to simulate melting penetration on Fe-U system. The MPS-LER modelled the eutectic phenomenon by solving the diffusion process and by applying the binary phase diagram criteria. This study simulates the melting penetration of the system at higher temperature using MPS-LER. Simulations were conducted on SS304 at 1400, 1450 and 1500°C. The simulation results show rapid increase of melting penetration rate. (paper)

  2. Biomedical implications of heavy metals induced imbalances in redox systems.

    Science.gov (United States)

    Sharma, Bechan; Singh, Shweta; Siddiqi, Nikhat J

    2014-01-01

    Several workers have extensively worked out the metal induced toxicity and have reported the toxic and carcinogenic effects of metals in human and animals. It is well known that these metals play a crucial role in facilitating normal biological functions of cells as well. One of the major mechanisms associated with heavy metal toxicity has been attributed to generation of reactive oxygen and nitrogen species, which develops imbalance between the prooxidant elements and the antioxidants (reducing elements) in the body. In this process, a shift to the former is termed as oxidative stress. The oxidative stress mediated toxicity of heavy metals involves damage primarily to liver (hepatotoxicity), central nervous system (neurotoxicity), DNA (genotoxicity), and kidney (nephrotoxicity) in animals and humans. Heavy metals are reported to impact signaling cascade and associated factors leading to apoptosis. The present review illustrates an account of the current knowledge about the effects of heavy metals (mainly arsenic, lead, mercury, and cadmium) induced oxidative stress as well as the possible remedies of metal(s) toxicity through natural/synthetic antioxidants, which may render their effects by reducing the concentration of toxic metal(s). This paper primarily concerns the clinicopathological and biomedical implications of heavy metals induced oxidative stress and their toxicity management in mammals.

  3. Biomedical Implications of Heavy Metals Induced Imbalances in Redox Systems

    Directory of Open Access Journals (Sweden)

    Bechan Sharma

    2014-01-01

    Full Text Available Several workers have extensively worked out the metal induced toxicity and have reported the toxic and carcinogenic effects of metals in human and animals. It is well known that these metals play a crucial role in facilitating normal biological functions of cells as well. One of the major mechanisms associated with heavy metal toxicity has been attributed to generation of reactive oxygen and nitrogen species, which develops imbalance between the prooxidant elements and the antioxidants (reducing elements in the body. In this process, a shift to the former is termed as oxidative stress. The oxidative stress mediated toxicity of heavy metals involves damage primarily to liver (hepatotoxicity, central nervous system (neurotoxicity, DNA (genotoxicity, and kidney (nephrotoxicity in animals and humans. Heavy metals are reported to impact signaling cascade and associated factors leading to apoptosis. The present review illustrates an account of the current knowledge about the effects of heavy metals (mainly arsenic, lead, mercury, and cadmium induced oxidative stress as well as the possible remedies of metal(s toxicity through natural/synthetic antioxidants, which may render their effects by reducing the concentration of toxic metal(s. This paper primarily concerns the clinicopathological and biomedical implications of heavy metals induced oxidative stress and their toxicity management in mammals.

  4. Tribo-systems for Sheet Metal Forming

    DEFF Research Database (Denmark)

    Bay, Niels

    2009-01-01

    The present paper gives an overview of more than 10 years work by the author’s research group through participation in national as well as international framework programmes on developing and testing environmentally friendly lubricants and tool materials and coatings inhibiting galling. Partners ......’s research group has especially been involved in the development of a system of tribo-tests for sheet metal forming and in testing and modelling of friction and limits of lubrication of new, environmentally friendly lubricants and tool materials.......The present paper gives an overview of more than 10 years work by the author’s research group through participation in national as well as international framework programmes on developing and testing environmentally friendly lubricants and tool materials and coatings inhibiting galling. Partners...... in the programmes come from Germany, United Kingdom, Finland, Poland, Slovenia, Spain and Denmark. They represent lubricant developers, testing experts and industrial end users as well as numerical modelling experts simulating fundamental lubrication mechanisms and computing basic process parameters. The author...

  5. Bioresorbable Ca-phosphate-polymer/metal and Fe-Ag nanocomposites for macro-porous scaffolds with tunable degradation and drug release

    Science.gov (United States)

    Gotman, I.; Swain, S. K.; Sharipova, A.; Gutmanas, E. Y.

    2016-11-01

    Bioresorbable implants are increasingly gaining popularity as an attractive alternative to traditional permanent bone healing devices. The advantage of bioresorbable implantable devices is that they slowly degrade over time and disappear once their "mission" is accomplished. Thus, no foreign material is left behind that can cause adverse effects on the host, such as long term local or systemic immune response and stress-shielding related bone atrophy. Resorbable materials considered for surgical implant applications include degradable polymers, Ca phosphate ceramics (CaP) and corrodible metals. Degradable polymers, such as polycaprolactone and lactic acid are weak, lack osteoconductivity and degrade to acidic products that can cause late inflammation. Resorbable CaP ceramics (e.g., β-TCP) are attractive materials for bone regeneration bear close resemblance to the bone mineral, however they are intrinsically brittle and thus unsuitable for use in load-bearing sites. Moreover, introducing high porosity required to encourage better cellular ingrowth into bone regeneration scaffolds is detrimental to the mechanical strength of the material. In present work we review and discuss our results on development of strong bioresorbable Ca-phosphate-polymer/metal nanonocomposites and highly porous scaffolds from them. By introduction of nanoscale ductile polymer or metal phase into CaP ceramic an attempt was made to mimic structure of natural bone, where nanocrystallites of CaP ceramic are bonded by thin collagen layers. Recent results on development of high strength scaffolds from Fe-Ag nanocomposites are also reported. High energy milling of powders followed by cold sintering—high pressure consolidation at ambient temperature in combination with modified porogen leaching method was employed for processing. The developed nanocomposites and scaffolds exhibited high mechanical strength coupled with measurable ductility, gradual lost weight and strength during immersion in

  6. Effect of local atomic disorder on the half-metallicity of full-Heusler Co2FeSi alloy: a first-principles study

    International Nuclear Information System (INIS)

    Guan-Nan, Li; Ying-Jiu, Jin; Il, Lee Jae

    2010-01-01

    This paper investigates the effect of atomic disorder on the electronic structure, magnetism, and half-metallicity of full-Heusler Co 2 FeSi alloy by using the full-potential linearized augmented plane wave method within the generalized gradient approximation (GGA) and GGA+U schemes. It considers three types of atomic disorders in Co 2 FeSi alloy: the Co–Fe, Co–Si, and Fe–Si disorders. Total energy calculations show that of the three types of disorders, the Fe–Si disorder is more likely to occur. It finds that for the Co–Si disorder, additional states appear in the minority band-gap at the E F and the half-metallcity is substantially destroyed, regardless of the disorder level. On the other hand, the Co–Fe and Fe–Si disorders have little effect on the half-metallicity at a low disorder level. When increasing the disorder levels, the half-metallcity is destroyed at about 9 % of the Co–Fe disorder level, while that stays at 25 % of the Fe–Si disorder level. (condensed matter: electronic structure, electrical, magnetic, and optical properties)

  7. Microstructure and High Temperature Oxidation Property of Fe-Cr-B Based Metal/Ceramic Composite Manufactured by Powder Injection Molding Process

    Science.gov (United States)

    Joo, Yeun-Ah; Kim, Young-Kyun; Yoon, Tae-Sik; Lee, Kee-Ahn

    2018-02-01

    This study investigated the microstructure and high temperature oxidation property of Fe-Cr-B metal/ceramic composite manufactured using powder injection molding process. Observations of initial microstructure showed a unique structure where α-Fe and (Cr, Fe)2B form a continuous three-dimensional network. High temperature oxidation tests were performed at 900, 1000 and 1100 °C, for 24 h, and the oxidation weight gain according to each temperature condition was 0.13, 0.84 and 6.4 mg/cm2, respectively. The oxidation results according to time at 900 and 1000 °C conditions represented parabolic curves, and at 1100 °C condition formed a rectilinear curve. Observation and phase analysis results of the oxides identified Cr2O3 and SiO2 at 900 and 1000 °C. In addition to Cr2O3 and SiO2, CrBO3 and FeCr2O4 formed due to phase decomposition of boride were identified at 1100 °C. Based on the findings above, this study suggested the high temperature oxidation mechanism of Fe-Cr-B metal/ceramic composite manufactured using powder injection molding, and the possibility of its application as a high temperature component material was also discussed.

  8. Microstructure and High Temperature Oxidation Property of Fe-Cr-B Based Metal/Ceramic Composite Manufactured by Powder Injection Molding Process

    Science.gov (United States)

    Joo, Yeun-Ah; Kim, Young-Kyun; Yoon, Tae-Sik; Lee, Kee-Ahn

    2018-03-01

    This study investigated the microstructure and high temperature oxidation property of Fe-Cr-B metal/ceramic composite manufactured using powder injection molding process. Observations of initial microstructure showed a unique structure where α-Fe and (Cr, Fe)2B form a continuous three-dimensional network. High temperature oxidation tests were performed at 900, 1000 and 1100 °C, for 24 h, and the oxidation weight gain according to each temperature condition was 0.13, 0.84 and 6.4 mg/cm2, respectively. The oxidation results according to time at 900 and 1000 °C conditions represented parabolic curves, and at 1100 °C condition formed a rectilinear curve. Observation and phase analysis results of the oxides identified Cr2O3 and SiO2 at 900 and 1000 °C. In addition to Cr2O3 and SiO2, CrBO3 and FeCr2O4 formed due to phase decomposition of boride were identified at 1100 °C. Based on the findings above, this study suggested the high temperature oxidation mechanism of Fe-Cr-B metal/ceramic composite manufactured using powder injection molding, and the possibility of its application as a high temperature component material was also discussed.

  9. Organometallic Routes into the Nanorealms of Binary Fe-Si Phases

    Directory of Open Access Journals (Sweden)

    Teddy M. Keller

    2010-02-01

    Full Text Available The Fe-Si binary system provides several iron silicides that have varied and exceptional material properties with applications in the electronic industry. The well known Fe-Si binary silicides are Fe3Si, Fe5Si3, FeSi, a-FeSi2 and b-FeSi2. While the iron-rich silicides Fe3Si and Fe5Si3 are known to be room temperature ferromagnets, the stoichiometric FeSi is the only known transition metal Kondo insulator. Furthermore, Fe5Si3 has also been demonstrated to exhibit giant magnetoresistance (GMR. The silicon-rich b-FeSi2 is a direct band gap material usable in light emitting diode (LED applications. Typically, these silicides are synthesized by traditional solid-state reactions or by ion beam-induced mixing (IBM of alternating metal and silicon layers. Alternatively, the utilization of organometallic compounds with reactive transition metal (Fe-carbon bonds has opened various routes for the preparation of these silicides and the silicon-stabilized bcc- and fcc-Fe phases contained in the Fe-Si binary phase diagram. The unique interfacial interactions of carbon with the Fe and Si components have resulted in the preferential formation of nanoscale versions of these materials. This review will discuss such reactions.

  10. Organometallic Routes into the Nanorealms of Binary Fe-Si Phases

    Science.gov (United States)

    Kolel-Veetil, Manoj K.; Keller, Teddy M.

    2010-01-01

    The Fe-Si binary system provides several iron silicides that have varied and exceptional material properties with applications in the electronic industry. The well known Fe-Si binary silicides are Fe3Si, Fe5Si3, FeSi, α-FeSi2 and β-FeSi2. While the iron-rich silicides Fe3Si and Fe5Si3 are known to be room temperature ferromagnets, the stoichiometric FeSi is the only known transition metal Kondo insulator. Furthermore, Fe5Si3 has also been demonstrated to exhibit giant magnetoresistance (GMR). The silicon-rich β-FeSi2 is a direct band gap material usable in light emitting diode (LED) applications. Typically, these silicides are synthesized by traditional solid-state reactions or by ion beam-induced mixing (IBM) of alternating metal and silicon layers. Alternatively, the utilization of organometallic compounds with reactive transition metal (Fe)-carbon bonds has opened various routes for the preparation of these silicides and the silicon-stabilized bcc- and fcc-Fe phases contained in the Fe-Si binary phase diagram. The unique interfacial interactions of carbon with the Fe and Si components have resulted in the preferential formation of nanoscale versions of these materials. This review will discuss such reactions.

  11. Adsorption geometry, conformation, and electronic structure of 2H-octaethylporphyrin on Ag(111) and Fe metalation in ultra high vacuum.

    Science.gov (United States)

    Borghetti, Patrizia; Di Santo, Giovanni; Castellarin-Cudia, Carla; Fanetti, Mattia; Sangaletti, Luigi; Magnano, Elena; Bondino, Federica; Goldoni, Andrea

    2013-04-14

    Due to the growing interest in the ferromagnetic properties of Fe-octaethylporphyrins (Fe-OEP) for applications in spintronics, methods to produce stable Fe-porphyrins with no Cl atoms are highly demanded. Here, we demonstrate the formation of Fe-OEP layers on Ag(111) single crystal by the ultra high vacuum in situ metalation of the free-base 2H-2,3,7,8,12,13,17,18-octaethylporphyrin (2H-OEP) molecules. The metalation proceeds exactly as in the case of 2H-5,10,15,20-tetraphenylporphyrin (2H-TPP) on the same substrate. An extensive surface characterization by means of X-ray photoemission spectroscopy, valence band photoemission, and NEXAFS with synchrotron radiation light provides information on molecular conformation and electronic structure in the monolayer and multilayer cases. We demonstrate that the presence of the ethyl groups affects the tilt of the adsorbed molecules, the conformation of the macrocycle, and the polarization screening in multilayers, but has only a minor effect in the metalation process with respect to 2H-TPP.

  12. Induced magnetism in transition metal intercalated graphitic systems

    KAUST Repository

    Kaloni, Thaneshwor P.

    2011-10-26

    We investigate the structure, chemical bonding, electronic properties, and magnetic behavior of a three-dimensional graphitic network in aba and aaa stacking with intercalated transition metal atoms (Mn, Fe, Co, Ni, and Cu). Using density functional theory, we find induced spin-polarization of the C atoms both when the graphene sheets are aba stacked (forming graphite) and aaa stacked (resembling bi-layer graphene). The magnetic moment induced by Mn, Fe, and Co turns out to vary from 1.38 μB to 4.10 μB, whereas intercalation of Ni and Cu does not lead to a magnetic state. The selective induction of spin-polarization can be utilized in spintronic and nanoelectronic applications.

  13. High pressure in situ diffraction studies of metal-hydrogen systems

    Energy Technology Data Exchange (ETDEWEB)

    Yartys, V.A., E-mail: volodymyr.yartys@ife.no [Institute for Energy Technology, Kjeller NO 2027 (Norway); Norwegian University of Science and Technology, Trondheim NO 7491 (Norway); Denys, R.V. [Institute for Energy Technology, Kjeller NO 2027 (Norway); Karpenko Physico-Mechanical Institute, NAS of Ukraine, Lviv 79601 (Ukraine); Webb, C.J. [Queensland Micro- and Nanotechnology Centre, Griffith University (Australia); Maehlen, J.P. [Institute for Energy Technology, Kjeller NO 2027 (Norway); Gray, E. MacA.; Blach, T. [Queensland Micro- and Nanotechnology Centre, Griffith University (Australia); Isnard, O. [Institute Neel, CNRS/UJF, 38042 Grenoble (France); Barnsley, L.C. [Queensland Micro- and Nanotechnology Centre, Griffith University (Australia)

    2011-09-15

    Research highlights: > CeNi{sub 5}-D{sub 2} and Zr(Fe,Al){sub 2}-D{sub 2} systems were studied by in situ NPD at P up to 1000 bar. > In the hexagonal CeNi{sub 5}D{sub 6.3} deuterium atoms fill three types of interstices. > In the Zr(Fe,Al){sub 2}-based deuterides D atoms occupy the Zr(Fe,Al){sub 2} tetrahedra only D/Zr(Fe,Al){sub 2}, hysteresis and hydrides stability systematically change with Al content. - Abstract: 'Hybrid' hydrogen storage, where hydrogen is stored in both the solid material and as a high pressure gas in the void volume of the tank can improve overall system efficiency by up to 50% compared to either compressed hydrogen or solid materials alone. Thermodynamically, high equilibrium hydrogen pressures in metal-hydrogen systems correspond to low enthalpies of hydrogen absorption-desorption. This decreases the calorimetric effects of the hydride formation-decomposition processes which can assist in achieving high rates of heat exchange during hydrogen loading-removing the bottleneck in achieving low charging times and improving overall hydrogen storage efficiency of large hydrogen stores. Two systems with hydrogenation enthalpies close to -20 kJ/mol H{sub 2} were studied to investigate the hydrogenation mechanism and kinetics: CeNi{sub 5}-D{sub 2} and ZrFe{sub 2-x}Al{sub x} (x = 0.02; 0.04; 0.20)-D{sub 2}. The structure of the intermetallics and their hydrides were studied by in situ neutron powder diffraction at pressures up to 1000 bar and complementary X-ray diffraction. The deuteration of the hexagonal CeNi{sub 5} intermetallic resulted in CeNi{sub 5}D{sub 6.3} with a volume expansion of 30.1%. Deuterium absorption filled three different types of interstices, Ce{sub 2}Ni{sub 2} and Ni{sub 4} tetrahedra, and Ce{sub 2}Ni{sub 3} half-octahedra and was accompanied by a valence change for Ce. Significant hysteresis was observed between deuterium absorption and desorption which profoundly decreased on a second absorption cycle. For the Al

  14. High pressure in situ diffraction studies of metal-hydrogen systems

    International Nuclear Information System (INIS)

    Yartys, V.A.; Denys, R.V.; Webb, C.J.; Maehlen, J.P.; Gray, E. MacA.; Blach, T.; Isnard, O.; Barnsley, L.C.

    2011-01-01

    Research highlights: → CeNi 5 -D 2 and Zr(Fe,Al) 2 -D 2 systems were studied by in situ NPD at P up to 1000 bar. → In the hexagonal CeNi 5 D 6.3 deuterium atoms fill three types of interstices. → In the Zr(Fe,Al) 2 -based deuterides D atoms occupy the Zr(Fe,Al) 2 tetrahedra only D/Zr(Fe,Al) 2 , hysteresis and hydrides stability systematically change with Al content. - Abstract: 'Hybrid' hydrogen storage, where hydrogen is stored in both the solid material and as a high pressure gas in the void volume of the tank can improve overall system efficiency by up to 50% compared to either compressed hydrogen or solid materials alone. Thermodynamically, high equilibrium hydrogen pressures in metal-hydrogen systems correspond to low enthalpies of hydrogen absorption-desorption. This decreases the calorimetric effects of the hydride formation-decomposition processes which can assist in achieving high rates of heat exchange during hydrogen loading-removing the bottleneck in achieving low charging times and improving overall hydrogen storage efficiency of large hydrogen stores. Two systems with hydrogenation enthalpies close to -20 kJ/mol H 2 were studied to investigate the hydrogenation mechanism and kinetics: CeNi 5 -D 2 and ZrFe 2-x Al x (x = 0.02; 0.04; 0.20)-D 2 . The structure of the intermetallics and their hydrides were studied by in situ neutron powder diffraction at pressures up to 1000 bar and complementary X-ray diffraction. The deuteration of the hexagonal CeNi 5 intermetallic resulted in CeNi 5 D 6.3 with a volume expansion of 30.1%. Deuterium absorption filled three different types of interstices, Ce 2 Ni 2 and Ni 4 tetrahedra, and Ce 2 Ni 3 half-octahedra and was accompanied by a valence change for Ce. Significant hysteresis was observed between deuterium absorption and desorption which profoundly decreased on a second absorption cycle. For the Al-modified Laves-type C15 ZrFe 2-x Al x intermetallics, deuteration showed very fast kinetics of H/D exchange

  15. Fabrication of metallic alloy powder (Ni{sub 3}Fe) from Fe–77Ni scrap

    Energy Technology Data Exchange (ETDEWEB)

    Seo, Inseok [ES Materials Research Center, Research Institute of Industrial Science and Technology, Incheon 406-840 (Korea, Republic of); Shin, Shun-Myung [Extractive Metallurgy Department, Korea Institute of Geoscience and Mineral Resources, Deajeon 305-350 (Korea, Republic of); Ha, Sang-An [Department of Environmental Engineering, Silla University, Busan 46958 (Korea, Republic of); Wang, Jei-Pil, E-mail: jpwang@pknu.ac.kr [Department of Metallurgical Engineering, Pukyong National University, Busan 608-739 (Korea, Republic of)

    2016-06-15

    The oxidation behavior of Fe–77Ni alloy scrap was investigated at an oxygen partial pressure of 0.2 atm and temperatures ranging from 400 °C to 900 °C. The corresponding oxidation rate increased with increasing temperature and obeyed the parabolic rate law, as evidenced by its linear proportionality to the temperature. In addition, surface morphologies, cross-sectional views, compositions, structural properties were examined by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), and X-ray diffraction (XRD). Diffusion through either the spinel structure or the NiO layer, which were both present in the alloy during oxidation at elevated temperatures, was deemed the rate-limiting step of the reaction. The oxide powder less than 10 μm was obtained from Fe–77Ni alloy scrap was obtained using ball-milling and sieving processes. In fact, 15 h of milling yielded a recovery ratio of 97%. Using hydrogen gas, the oxide powder was successfully reduced to an alloy powder of Ni{sub 3}Fe and reduction rates of ∼97% were achieved after 3 h at 1000 °C. - Highlights: • The oxidation behavior of Fe–77Ni alloy scrap was investigated. • The oxide powder less than 10 μm was obtained from Fe–77Ni alloy scrap. • Using hydrogen gas, the oxide powder was successfully reclaimed. • Reduction rates of ∼97% were achieved after 3 h at 1000 °C.

  16. Electric field as a novel switch for magnetization of Fe/graphene system

    International Nuclear Information System (INIS)

    Yun, Kyung-Han; Lee, Minho; Chung, Yong-Chae

    2014-01-01

    The magnetic property of a graphene-adsorbed Fe adatom was observed under an external electric field effect (−0.3–0.3 eV/Å) using density functional theory (DFT) calculations. In this study, it was demonstrated that the magnetic moment of Fe on graphene was changed linearly according to the electric field. The density of states and differential planar-averaged charge-density indicated that the changing electronic structure was due to a redistribution of valence electrons under external electric field that induces a continuous change in the localized magnetic moment of the Fe adatom. This research suggests that the magnetic property of the adatom on graphene is tunable by an electric field. Furthermore, these results may be applicable to the spintronic memory device industry. - Highlights: • E-field effect on the magnetic property of Fe/graphene was investigated. • Magnetic moment of Fe adatom changed continuously according to E-field. • Change in magnetic property is caused by the charge redistribution in Fe/graphene system. • Understanding of E-field effect offers a clear view for spintronics applications

  17. Energy for the interface system of (Nb, Mo)C/γ-Fe

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Yanyuan; Wang, Zhenqiang; Zhao, Jiaying; Niu, Zhongyi; Guo, Chunhuan; Jiang, Fengchun [Harbin Engineering University, Key Laboratory of Superlight Materials and Surface Technology, Ministry of Education, College of Material Science and Chemical Engineering, Harbin (China); Leng, Zhe [Harbin Engineering University, Key Laboratory of Superlight Materials and Surface Technology, Ministry of Education, College of Material Science and Chemical Engineering, Harbin (China); Zhejiang Ocean University, Innovation and Application Institute, Zhoushan (China); Zhang, Zhengyan; Yao, Chunfa [Central Iron and Steel Research Institute, Department of Structural Steels, Beijing (China); Yang, Zhigang [Tsinghua University, Key Laboratory of Advanced Materials, School of Materials Science and Engineering, Beijing (China)

    2017-08-15

    The interfacial energies of MC/γ-Fe and formation energies of MC carbides have been investigated using first-principles calculations based on density functional theory (DFT). Results show that the replacement of Nb by Mo in the NbC lattice is unfavorable with respect to the formation energy. However, it reduces the lattice parameter of MC and decreases the σ{sub chemical} (interfacial chemical energy) of MC/γ-Fe, thus favoring the formation of complex (Nb, Mo)C carbide. The substitution of Nb by Mo at the interface of MC/γ-Fe system promotes the hybridizations of Mo-1NNFe and C-1NNFe (or 2NNFe) (the first or second nearest neighboring Fe atoms), which leads to a decrease in σ{sub chemical}. The influence of bond energy is estimated using the discrete lattice plane/nearest neighbor broken bond (DLP/NNBB) model. It is found that the reduced is attributed to the much smaller value of e{sub Fe-C}-e{sub Mo-C} (the difference between Fe-C and Nb-C interactions). The results obtained from the analysis of the precipitates in Nb- and Nb-Mo-bearing steels are in a good agreement with the calculations. (orig.)

  18. Calculation of solidification microstructure maps for the system Al-Fe-Si

    International Nuclear Information System (INIS)

    Gilgien, P.

    1996-01-01

    Computer programs have been developed in order to calculate solidification microstructure maps for binary and ternary alloys. These programs are based on recent analytical models for the constrained growth of dendrites and eutectics. Due to the importance of phase diagrams data, programs for the calculation of growth kinetics are coupled with ThermoCalc, a commercial software for phase diagram calculations. These programs have been used to calculate a solidification microstructure map for the Al-Fe system from 0 to 4 at%Fe. Comparison of the calculated results with an experimental solidification microstructure map from the literature shows that all microstructure transitions were predicted. Nevertheless there remain significant discrepancies between some calculated and experimental transition velocities. The programs were also used to calculate solidification microstructure maps in the Al-rich corner of the Al-Fe-Si system (0 to 8 at% Fe and 0 to 8 at% Si). In this case also, calculated results were in satisfactory agreement with experimental solidification microstructure maps, although the comparison was only partial since experimental ternary microstructure maps are less complete than for the binary system, and because the available thermodynamic database does not, as yet, include metastable phases. Laser surface remelting experiments were carried out on an Al-4 at% Fe alloy in order to link results from the literature, obtained at high solidification rates by laser surface remelting and at low solidification rates by Bridman experiments. Finally, Bridman experiments were carried out with an Al-2.63 wt% Fe alloy in order to determine the critical velocity at which a planar Al-Al 13 Fe 4 eutectic front is destabilised in a cellular eutectic by a small amount of Si. The critical solidification velocity thus obtained was in agreement with a criterion of constitutional undercooling. (author) figs., tabs., refs

  19. Charge transfer in gold--alkali-metal systems

    International Nuclear Information System (INIS)

    Watson, R.E.; Weinert, M.

    1994-01-01

    Based on conventional electronegativity arguments, gold--alkali-metal compounds are expected to be among the most ''ionic'' of metallic compounds. The concepts of ionicity and charge transfer are difficult to quantify. However, the changes in bonding in the 50/50 Au--alkali-metal systems between the elemental metals and the compounds are so severe that observations can readily be made concerning their character. The results, as obtained from self-consistent electronic-structure calculations, lead to the apparently odd observation that the electron density at the alkali-metal sites in the compound increases significantly and this involves high l componennts in the charge density. This increase, however, can be attributed to Au-like orbitals spatially overlapping the alkali-metal sites. In a chemical sense, it is reasonable to consider the alkali-metal transferring charge to these Au orbitals. While normally the difference in heats of formation between muffin-tin and full-potential calculations for transition-metal--transition-metal and transition-metal--main-group (e.g., Al) compounds having high site symmetry are small, for the gold--alkali-metal systems, the changes in bonding in the compounds cause differences of ∼0.5 eV/atom between the two classes of potential. Any serious estimate of the electronic structure in these systems must account for these aspherical bonding charges. The origin of the semiconducting behavior of the heavy-alkali-metal Au compounds is shown to arise from a combination of the Au-Au separations and the ionic character of the compounds; the light-alkali-metal Au compounds, with their smaller Au-Au separations, do not have a semiconducting gap. Core-level shifts and isomer shifts are also briefly discussed

  20. Porous Fe21Cr7Al1Mo0.5Y metal supports for oxygen transport membranes: Thermo-mechanical properties, sintering and corrosion behaviour

    DEFF Research Database (Denmark)

    Glasscock, Julie; Mikkelsen, Lars; Persson, Åsa Helen

    2013-01-01

    An Fe21Cr7Al1Mo0.5Y alumina-forming stainless steel is designed and evaluated as a material for porous supports for oxygen transport membranes. The thermal expansion coefficient, elastic modulus and creep rates of the alloy are presented. The microstructure, porosity and pre-oxidation conditions...... resistance compared with an FeCr steel of similar composition and porosity. Modelling of the alloy lifetime as a function of surface area and Al-content was performed, and lifetimes over 30 000 h are predicted for a metal support with 30% porosity operating at a temperature of 750 C, where the oxidation...

  1. Presence of 60Fe in eucrite Piplia Kalan: A new perspective to the initial 60Fe/ 56Fe in the early solar system

    Digital Repository Service at National Institute of Oceanography (India)

    Rudraswami, N.G.; Sahijpal, S.; Bhandari, N.

    /Ma in the crust region of the parent body of Piplia Kalan, thereby matching the initial sup(60) Fe/sup(56) Fe to approx. 5 × 10 sup(-7). This is consistent with the initial value found in the silicate phases in chondrules of least metamorphosed meteorites. However...

  2. Melting phase relations in the Fe-S and Fe-S-O systems at core conditions in small terrestrial bodies

    Science.gov (United States)

    Pommier, Anne; Laurenz, Vera; Davies, Christopher J.; Frost, Daniel J.

    2018-05-01

    We report an experimental investigation of phase equilibria in the Fe-S and Fe-S-O systems. Experiments were performed at high temperatures (1400-1850 °C) and high pressures (14 and 20 GPa) using a multi-anvil apparatus. The results of this study are used to understand the effect of sulfur and oxygen on core dynamics in small terrestrial bodies. We observe that the formation of solid FeO grains occurs at the Fe-S liquid - Fe solid interface at high temperature ( > 1400 °C at 20 GPa). Oxygen fugacities calculated for each O-bearing sample show that redox conditions vary from ΔIW = -0.65 to 0. Considering the relative density of each phase and existing evolutionary models of terrestrial cores, we apply our experimental results to the cores of Mars and Ganymede. We suggest that the presence of FeO in small terrestrial bodies tends to contribute to outer-core compositional stratification. Depending on the redox and thermal history of the planet, FeO may also help form a transitional redox zone at the core-mantle boundary.

  3. Thermodynamic study of sodium-iron oxides. Part 2. Ternary phase diagram of the Na-Fe-O system

    International Nuclear Information System (INIS)

    Huang, Jintao; Furukawa, Tomohiro; Aoto, Kazumi

    2003-01-01

    Studies on ternary phase diagrams of the Na-Fe-O system have been carried out from the thermodynamic point of view. Thermodynamic data of main ternary Na-Fe oxides Na 4 FeO 3 (s), Na 3 FeO 3 (s), Na 5 FeO 4 (s) and Na 8 Fe 2 O 7 (s) have been assessed. A user database has been created by reviewing literature data together with recent DSC and vapor pressure measurements by the present authors. New ternary phase diagrams of the Na-Fe-O system have been constructed from room temperature to 1000K. Stable conditions of the ternary oxides at 800K were presented in predominance diagram as functions of oxygen pressure and sodium pressure

  4. Precious metal enrichment at low-redox in terrestrial native Fe-bearing basalts investigated using laser-ablation ICP-MS

    Science.gov (United States)

    Howarth, Geoffrey H.; Day, James M. D.; Pernet-Fisher, John F.; Goodrich, Cyrena A.; Pearson, D. Graham; Luo, Yan; Ryabov, Viktor V.; Taylor, Lawrence A.

    2017-04-01

    Primary native Fe is a rare crystallizing phase from terrestrial basaltic magmas, requiring highly reducing conditions (fO2 abundances. Three localities are known globally where native Fe bearing mafic rocks occur: (1) Paleocene basalts of Disko Island, West Greenland; (2) a Miocene lava of the Bühl basalts, Germany; and (3) mafic intrusions associated with the Late Permian Siberian flood basalts. In this contribution, we report major- and minor-element compositions and HSE concentrations for the main alloy phases (FeNi metal and cohenite) and sulfide, for all three known global occurrences of native Fe bearing basalt. Total HSE abundances in metal grains, obtained by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), are lowest in the Bühl basalt, (∼0.05 ppm), intermediate in the Disko Island basalts (4-8 ppm), and highest the Siberian Khungtukun and Dzhaltul intrusions (10-30 ppm). These differences demonstrate that, while native Fe formation is the result of carbonaceous crustal assimilation, HSE enrichment is not ubiquitous during this process. The Siberian occurrences are characterized by Pt PGE (PPGE: Pt, Pd) enrichment relative to the Ir PGE (IPGE: Rh, Ru, Ir, Os), consistent with models of early stage fractionation of olivine, chromite and metallic IPGE in staging magma reservoirs, prior to the addition of C-rich crustal materials in the shallow crust. Relative to Noril'sk Ni-Cu-PGE sulfide ores, the Siberian native Fe basalts are enriched in the PPGE relative to the IPGE, but exhibit Ru enrichments. In contrast, Disko Island native Fe rocks do not show significant fractionation of the PPGE from the IPGE, but have positive Re and Ru anomalies and high Os/Ir ratios. To reconcile these observations, we present a general model where some parental melts experienced early-stage crustal assimilation in staging magma reservoirs, prior to reduction by carbon-rich materials (e.g., Khungtukun, Dzhaltul), whereas basaltic parental melts to

  5. Nano-sized Fe-metal catalyst on ZnO-SiO2: (photo-assisted deposition and impregnation) Synthesis routes and nanostructure characterization

    International Nuclear Information System (INIS)

    Mohamed, R.M.; Al-Rayyani, M.A.; Baeissa, E.S.; Mkhalid, I.A.

    2011-01-01

    Highlights: → We prepared Fe/ZnO-SiO 2 by two methods. → We tested photocatalytic activity for degradation of methylene blue dye. → We controlled band gap and size. → We found activity of Fe/ZnO-SiO 2 prepared by PAD is hightest photocatalytic activity. - Abstract: A nano-sized Fe metal on ZnO-SiO 2 was synthesized using the photo-assisted deposition (PAD) and impregnation routes. The obtained samples were characterized by a series of techniques including X-ray diffraction (XRD), UV-vis diffuse reflectance spectroscopy, N 2 adsorption, extended X-ray absorption fine structure (EXAFS), and transmission electron microscopy (TEM). Photocatalytic reactivity using Fe-ZnO-SiO 2 catalysts under visible-light condition on the degradation of methylene blue dye was evaluated. The results of characterization reveal, a notable photocatalytic activity of PAD:Fe-ZnO-SiO 2 which was about 9 and 12 times higher than that of Img:Fe-ZnO-SiO 2 and ZnO-SiO 2 , respectively.

  6. Metal Dependence of Signal Transmission through MolecularQuantum-Dot Cellular Automata (QCA: A Theoretical Studyon Fe, Ru, and Os Mixed-Valence Complexes

    Directory of Open Access Journals (Sweden)

    Ken Tokunaga

    2010-08-01

    Full Text Available Dynamic behavior of signal transmission through metal complexes [L5M-BL-ML5]5+ (M=Fe, Ru, Os, BL=pyrazine (py, 4,4’-bipyridine (bpy, L=NH3, which are simplified models of the molecular quantum-dot cellular automata (molecular QCA, is discussed from the viewpoint of one-electron theory, density functional theory. It is found that for py complexes, the signal transmission time (tst is Fe(0.6 fs < Os(0.7 fs < Ru(1.1 fs and the signal amplitude (A is Fe(0.05 e < Os(0.06 e < Ru(0.10 e. For bpy complexes, tst and A are Fe(1.4 fs < Os(1.7 fs < Ru(2.5 fs and Os(0.11 e < Ru(0.12 e <Fe(0.13 e, respectively. Bpy complexes generally have stronger signal amplitude, but waste longer time for signal transmission than py complexes. Among all complexes, Fe complex with bpy BL shows the best result. These results are discussed from overlap integral and energy gap of molecular orbitals.

  7. Organophosphorus flame retardants and heavy metals in municipal landfill leachate treatment system in Guangzhou, China.

    Science.gov (United States)

    Deng, Mingjun; Kuo, Dave T F; Wu, Qihang; Zhang, Ying; Liu, Xinyu; Liu, Shengyu; Hu, Xiaodong; Mai, Bixian; Liu, Zhineng; Zhang, Haozhi

    2018-05-01

    The occurrence, distribution and removal efficiencies of organophosphorus flame retardants (OPFRs) and metals were examined in a municipal landfill leachate treatment system in Guangzhou, China. Five OPFRs and thirty-five metals were detected in wastewater samples collected at different treatment stages. ∑OPFRs was reduced from 4807.02 ng L -1 to 103.91 ng L -1 through the treatment system, with close to 98% removed from the dissolved phase. Tris(clorisopropyl) phosphates (TCPPs) dominated through the treatment process and accounted for over 80% and 50% of ∑OPFRs at the influent and the effluent, respectively. TCPPs were most efficiently removed (98.6%) followed by tris(2-chloroethyl) phosphate (TCEP) (96.6%) and triphenyl phosphate (TPP) (88.5%). For metals, Fe, Cr, and Rb were dominant in the raw leachate, detected at 7.55, 2.82, and 4.50 mg L -1 , respectively. Thirteen regulated heavy metals - including eight major pollutants (i.e., As. Cd, Cr, Cu, Hg, Ni, Pb, and Zn) - have been detected in all wastewater samples at sub-mg L -1 levels. Over 99.5% removal was achieved for Cr, Ni, and Fe, and close to 95% removal efficiency was observed for Rb. For the eight major heavy metals, over 99% removal was observed; the only exception was Cu, which was removed at 89%. It was found that microfiltration/reverse osmosis was critical for the removal of OPFRs and heavy metals while the core biological treatment played a minor role towards their removal. Remobilization of Co, Cu, Fe, Hg, Mn, Ni, Sb, and Sr from the returned sludge occurred during the second denitrification, indicating the need for additional post-biological process for effective removal of both contaminants. This study highlights the critical need to develop cheap, effective treatment technologies for contaminants-laden leachate generated from open dumps and under-designed landfills. Copyright © 2018 Elsevier Ltd. All rights reserved.

  8. Drastic influence of minor Fe or Co additions on the glass forming ability, martensitic transformations and mechanical properties of shape memory Zr-Cu-Al bulk metallic glass composites.

    Science.gov (United States)

    González, Sergio; Pérez, Pablo; Rossinyol, Emma; Suriñach, Santiago; Dolors Baró, Maria; Pellicer, Eva; Sort, Jordi

    2014-06-01

    The microstructure and mechanical properties of Zr 48 Cu 48 -  x Al 4 M x (M ≡ Fe or Co, x  = 0, 0.5, 1 at.%) metallic glass (MG) composites are highly dependent on the amount of Fe or Co added as microalloying elements in the parent Zr 48 Cu 48 Al 4 material. Addition of Fe and Co promotes the transformation from austenite to martensite during the course of nanoindentation or compression experiments, resulting in an enhancement of plasticity. However, the presence of Fe or Co also reduces the glass forming ability, ultimately causing a worsening of the mechanical properties. Owing to the interplay between these two effects, the compressive plasticity for alloys with x  = 0.5 (5.5% in Zr 48 Cu 47.5 Al 4 Co 0.5 and 6.2% in Zr 48 Cu 47.5 Al 4 Fe 0.5 ) is considerably larger than for Zr 48 Cu 48 Al 4 or the alloys with x  = 1. Slight variations in the Young's modulus (around 5-10%) and significant changes in the yield stress (up to 25%) are also observed depending on the composition. The different microstructural factors that have an influence on the mechanical behavior of these composites are investigated in detail: (i) co-existence of amorphous and crystalline phases in the as-cast state, (ii) nature of the crystalline phases (austenite versus martensite content), and (iii) propensity for the austenite to undergo a mechanically-driven martensitic transformation during plastic deformation. Evidence for intragranular nanotwins likely generated in the course of the austenite-martensite transformation is provided by transmission electron microscopy. Our results reveal that fine-tuning of the composition of the Zr-Cu-Al-(Fe,Co) system is crucial in order to optimize the mechanical performance of these bulk MG composites, to make them suitable materials for structural applications.

  9. The Mount Wilson Observatory Metallicity Index, C RV: Comparison with Other Photometric Systems

    Science.gov (United States)

    Soon, W. H.; Zhang, Q.; Baliunas, S. L.; Kurucz, R. L.

    1993-10-01

    A new spectrophotometric index, CRV, is assessed as a metallicity indicator for late-type stars. The index is the ratio of the measured photospheric fluxes in 20 Å wide passbands centered at 400t and 3901 Å. CRV correlates directly with the metallicity index, m1, of the Strömgren uvby system and with the metallicity index hk, of Anthony-Twarog et al. (1991). Using observations of 236 dwarfs and 140 giants combined with stellar atmosphere models (Kurucz 1991), we compared the sensitivity of the CRV, m1, and hk indices to metal abundance. We also studied the sensitivity of the CRV, C1, and hk indices to surface gravity. The effect of interstellar extinction on all the indices was also studied from published mean extinction laws. We find that the CRV index is sensitive to the variation of metal abundance, [M], over the range examined (-5.0 ≲ [M] ≲ 0.5). CRV is also more sensitive than the m1 index at metal-poor conditions ([M] ≲ -2.0). The CRV index has the following advantages: (1) the passbands of CRV are dominated by Fe lines, which reduce the uncertainty that may be introduced by the presence of lines of α-process elements with enhanced abundances at metal-poor conditions; (2) the effect of interstellar reddening is limited because the two passbands are separated in wavelength by only 100 Å. We also find that the atmospheric models produce results that agree qualitatively with the trends of observed indices on stellar parameters such as effective temperature, metallicity, and surface gravity.

  10. Theoretical calculations of valence states in Fe-Mo compounds

    International Nuclear Information System (INIS)

    Estrada, F; Navarro, O; Noverola, H; Suárez, J R; Avignon, M

    2014-01-01

    The half-metallic ferromagnetic double perovskite compound Sr 2 FeMoO 6 is considered as an important material for spintronic applications. It appears to be fundamental to understand the role of electronic parameters controlling the half-metallic ground state. Fe-Mo double perovskites usually present some degree of Fe/Mo disorder which generally increases with doping. In this work, we study the valence states of Fe-Mo cations in the off-stoichiometric system Sr 2 Fe 1+x Mo 1−x O 6 (−1 ≤ x ≤ 1/3) with disorder. Our results for Fe and Mo valence states are obtained using the Green functions and the renormalization perturbation expansion method. The model is based on a correlated electron picture with localized Fe-spins and conduction Mo-electrons interacting with the local spins via a double-exchange-type mechanism

  11. The Distribution of Heavy Metal Pollutants in Suez Bay Using Geographic Information System (GIS)

    International Nuclear Information System (INIS)

    Hassan, H.B.; Mohamed, W.M.

    2017-01-01

    Suez city represents the southern entrance of the Suez Canal. As a result of the rapid development of industrialization and anthropogenic activities of Suez city may be entered containments such as heavy metals through Suez bay boundaries. The geographical information system (Arc GIS 9.1) is used to study the spatial distribution of heavy metals concentrations (Cd, Mn, Fe, Ni, Pb, Cu and Zn) of water samples which were collected in four different sampling sites (I, II, III and IV) from Suez bay. In this study, tabular data representation of the spatial distribution was developed using the inverse distance weighted (IDW) interpolation method. The GIS technique was applied to transfer the information into a final map illustrating the spatial distribution of heavy metals within the studied area. GIS models showed the high concentrations of heavy metals in some sites in the Suez city affecting by their activities. An overall distribution map of heavy metals is observed from GIS special analysis. Site (IV) in Suez City demonstrated the highest polluted are a in the overall distribution map

  12. Characterization of metal/humic acid systems by Capillary Electrophoresis

    NARCIS (Netherlands)

    Staden JJ van; Hoop MAGT van den; Cleven R; LAC

    2000-01-01

    Metal-humic acid systems have been characterised applying Capillary Electrophoresis (CE). Appropriate experimental conditions with respect to carrier electrolyte, pH range, salt concentration, humic acid concentration and the applied potential, have been optimised. The influence of multivalent metal

  13. Plasma arc systems for waste treatment and metal recovery

    Science.gov (United States)

    Eschenbach, Richard C.

    1996-06-01

    Plasma torches are being used for treating very difficult wastes,for recovering metal values from metallurgical wastes, and for making high-quality ingots and powder in the special metals industry. This article discusses the process requirements and the state of the art for plasma arc systems in each of these fields.

  14. Borides of the group 1 metals of the periodic system

    International Nuclear Information System (INIS)

    Samsonov, G.V.; Serebryakova, T.I.; Neronov, V.A.

    1975-01-01

    The borides of alkali metals (lithium, sodium, potassium) and the metals of a copper subgroup (copper, silver, gold) are described. Consideration is given to the crystalline structure and state diagrams of the metal systems within the first group of the Periodic Table with boron. Existence, formation conditions and physico-chemical properties of binary boride phases are characterized. Conclusion is made as to the absence of interaction between boron and silver. Information on the interaction between gold and boron is scanty and conflicting. Methods are described suitable for the production of the borides of the metals within the first group of the Periodic Table [ru

  15. High-nitrogen-metal complexes as burning-rate modifiers for the aluminum-water propellant system

    Energy Technology Data Exchange (ETDEWEB)

    Tappan, Bryce C [Los Alamos National Laboratory; Mason, Benjamin A [Los Alamos National Laboratory

    2009-01-01

    The reactions of electropositive metals, such as aluminum, with water have long been utilized in explosive and propellant formulations, but until recently this has mostly been limited to the water formed as a product gas from the decomposition of another energetic system . Recently, however, with the increased availability of nano-particulate materials, the direct reaction of nano-aluminum (nAl) with water as an oxidizer has been investigated as a propellant system due to high reaction temperatures and the production of hydrogen as the primary gaseous species. This system could be useful for intra-planetary travel where non-terrestrial water is harvested for the oxidizer. Here we present the study of nAl, mixed at a stoichiometric ratio with water ({Phi} = 1) with the highly water soluble metal complexes of bis(tetrazolato)amine (BTA) added at 5, 15,30 and 50 wt% in the case of FeBTA and 5 and 15 wt% in the case of NiBTA and CoBTA. The basic structure of the BTA complexes is shown below where M = Fe, Ni or Co, and x = 3 for Fe and Co and x = 2 for Ni. The particle size of nAl studied was primarily 38 nm with various studies with the particle size of 80 nm. The FeBT A at a loading of 15 wt% gave the highest burning rate enhancement (4.6x at {approx}6.8 MPa), while retaining a low pressure exponent (0.21 compared to 0.24 for nA/H{sub 2}O). At 15 wt% the Ni and Co increased the burning rate, but also increased the pressure exponents. The burning rate of the FeBTA modified material with 80 nm Al decreased as the weight percent of FeBTA was increased, which also tracked decrease in the calculated specific impulse of the mixtures.

  16. Cleanable sintered metal filters in hot off-gas systems

    International Nuclear Information System (INIS)

    Schurr, G.A.

    1981-01-01

    Filters with sintered metal elements, arranged as tube bundles with backflush air cleaning, are the equivalent of bag filters for high-temperature, harsh environments. They are virtually the only alternative for high-temperature off-gas systems where a renewable, highly efficient particle trap is required. Tests were conducted which show that the sintered metal elements installed in a filter system provide effective powder collection in high-temperature atmospheres over thousands of cleaning cycles. Such a sintered metal filter system is now installed on the experimental defense waste calciner at the Savannah River Laboratory. The experimental results included in this paper were used as the basis for its design

  17. Is Sm2Fe17Nx a two-phase system?

    International Nuclear Information System (INIS)

    Brennan, S.; Skomski, R.; Qi Qinian; Coey, J.M.D.

    1995-01-01

    Interstitial nitrides Sm 2 Fe 17 N x with x≤3 form gas-solid solutions independent of whether NH 3 or N 2 is used to produce them. The volume of well homogenised samples follows Vegard's law, and the Curie temperature is also linear in x. Ammonia facilitates the initial stage of the reaction by improving the effective surface activity of the metallic powder. A clear distinction is made between nitrides allowed to reach quasi-equlibrium at 425 C and those quenched to stop the reaction. ((orig.))

  18. Transport properties and pinning analysis for Co-doped BaFe2As2 thin films on metal tapes

    Science.gov (United States)

    Xu, Zhongtang; Yuan, Pusheng; Fan, Fan; Chen, Yimin; Ma, Yanwei

    2018-05-01

    We report on the transport properties and pinning analysis of BaFe1.84Co0.16As2 (Ba122:Co) thin films on metal tapes by pulsed laser deposition. The thin films exhibit a large in-plane misorientation of 5.6°, close to that of the buffer layer SrTiO3 (5.9°). Activation energy U 0(H) analysis reveals a power law relationship with field, having three different exponents at different field regions, indicative of variation from single-vortex pinning to a collective flux creep regime. The Ba122:Co coated conductors present {{T}{{c}}}{{onset}} = 20.2 K and {{T}{{c}}}{{zero}} = 19.0 K along with a self-field J c of 1.14 MA cm‑2 and an in-field J c as high as 0.98 and 0.86 MA cm‑2 up to 9 T at 4.2 K for both major crystallographic directions of the applied field, promising for high field applications. Pinning force analysis indicates a significant enhancement compared with similar Ba122:Co coated conductors. By using the anisotropic scaling approach, intrinsic pinning associated with coupling between superconducting blocks can be identified as the pinning source in the vicinity of H//ab, while for H//c random point defects are likely to play a role but correlated defects start to be active at high temperatures.

  19. Negative magnetoresistance in an antiferromagnetic metal β″-(EDO-TTFVODS) 2FeBr 4(DCE) 0.5

    Science.gov (United States)

    Weng, Yufeng; Yoshino, Harukazu; Fujiwara, Hideki; Sugimoto, Toyonari; Murata, Keizo

    2008-12-01

    An organic conductor β″-(EDO-TTFVODS) 2FeBr 4(DCE) 0.5, where EDO-TTFVODS is ethylenedioxytetrathiafulvalenoquinone-1,3-diselenolemethide and DCE is 1,2-dichloroethane, has been synthesized and is expected to have a strong π-d interaction. It was found that the material is metallic down to about 4 K and shows a rather slight upturn of electrical resistivity ρ below this temperature. Temperature dependence of ρ in the slight upturn region is proportional to log T and weak negative magnetoresistance (-1.7%, 2 T) at 1.4 K also appears. Besides π-d interaction screened by conducting electrons in this material, weak localization and Kondo effect are also possible to explain this negative magnetoresistance. Oscillatory behavior probably due to a quasi-two-dimensional (Q2D) Fermi surface was observed in the field-orientation dependence, and kF‖ b' was estimated to be 0.19 Å -1.

  20. Hydrogen Storage Properties of Metal Nitroprussides M[Fe(CN)5NO], (M = Co, Ni)

    Energy Technology Data Exchange (ETDEWEB)

    Culp, J T; Matranga, C S; Smith, M; Bittner, E W; Bockrath, B C

    2006-04-27

    The volumetric hydrogen adsorption isotherms of two isostructural dehydrated cubic metal nitroprussides M[Fe(CN)5NO] (M = Co2+, Ni2+) have been measured up to a pressure of 760 Torr at 77 and 87 K. These materials are among the most efficient H2 sorbents based on porous coordination polymers reported to date. The H2 uptake in both materials is ~1.6 wt % at 77 K and 760 torr. These H2 capacities match those reported recently in the structurally related M3[Co(CN)6]2 compounds and are approximately 25% higher than those reported for Zn4O(1,4-benzenedicarboxylate)3 under the same conditions of temperature and pressure. The isosteric heats of H2 adsorption calculated from the 77 and 87 K isotherms for both materials were found to vary from ~7.5 kJ/mol at 0.40 wt % coverage to ~5.5 kJ/mol at 1.2 wt % coverage. The N2 BET surface areas were determined to be 634 m2/g and 523 m2/g for M = Ni and M = Co, respectively.

  1. Metallic elements (Ca, Hg, Fe, K, Mg, Mn, Na, Zn) in the fruiting bodies of Boletus badius.

    Science.gov (United States)

    Kojta, Anna K; Falandysz, Jerzy

    2016-06-01

    The aim of this study was to investigate and compare the levels of eight metallic elements in the fruiting bodies of Bay Bolete (Boletus badius; current name Imleria badia) collected from ten sites in Poland to understand better the value of this popular mushroom as an organic food. Bay Bolete fruiting bodies were collected from the forest area near the towns and villages of Kętrzyn, Poniatowa, Bydgoszcz, Pelplin, Włocławek, Żuromin, Chełmno, Ełk and Wilków communities, as well as in the Augustów Primeval Forest. Elements such as Ca, Fe, K, Mg, Mn, Na and Zn were analyzed by inductively coupled plasma atomic emission spectroscopy (ICP-OES), and mercury by cold vapor atomic absorption spectrometry (CV-AAS). This made it possible to assess the nutritional value of the mushroom, as well as possible toxicological risks associated with its consumption. The results were subjected to statistical analysis (Kruskal-Wallis test, cluster analysis, principal component analysis). Copyright © 2016 Elsevier Ltd. All rights reserved.

  2. Effective Carbon Dioxide Photoreduction over Metals (Fe-, Co-, Ni-, and Cu- Incorporated TiO2/Basalt Fiber Films

    Directory of Open Access Journals (Sweden)

    Jeong Yeon Do

    2016-01-01

    Full Text Available Mineralogical basalt fibers as a complementary adsorbent were introduced to improve the adsorption of CO2 over the surfaces of photocatalysts. TiO2 photocatalysts (M-TiO2 incorporated with 5.0 mol.% 3d-transition metals (Fe, Co, Ni, and Cu were prepared using a solvothermal method and mixed with basalt fibers for applications to CO2 photoreduction. The resulting 5.0 mol.% M-TiO2 powders were characterized by X-ray diffraction, scanning electron microscopy, ultraviolet-visible spectroscopy, photoluminescence, Brunauer, Emmett, and Teller surface area, and CO2-temperature-programmed desorption. A paste composed of two materials was coated and fixed on a Pyrex plate by a thermal treatment. The 5.0 mol.% M-TiO2/basalt fiber films increased the adsorption of CO2 significantly, indicating superior photocatalytic behavior compared to pure TiO2 and basalt fiber films, and produced 158~360 μmol gcat-1 L−1 CH4 gases after an 8 h reaction. In particular, the best performance was observed over the 5.0 mol.% Co-TiO2/basalt fiber film. These results were attributed to the effective CO2 gas adsorption and inhibition of photogenerated electron-hole pair recombination.

  3. Molybdenum-tin as a solar cell metallization system

    Science.gov (United States)

    Boyd, D. W.; Radics, C.

    1981-01-01

    The operations of solar cell manufacture are briefly examined. The formation of reliable, ohmic, low-loss, and low-cost metal contacts on solar cells is a critical process step in cell manufacturing. In a commonly used process, low-cost metallization is achieved by screen printing a metal powder-glass frit ink on the surface of the Si surface and the conductive metal powder. A technique utilizing a molybdenum-tin alloy for the metal contacts appears to lower the cost of materials and to reduce process complexity. The ink used in this system is formulated from MoO3 with Sn powder and a trace amount of titanium resonate. Resistive losses of the resulting contacts are low because the ink contains no frit. The MoO3 is finally melted and reduced in forming gas (N2+H2) to Mo metal. The resulting Mo is highly reactive which facilitates the Mo-Si bonding.

  4. Resonant Auger studies of metallic systems

    International Nuclear Information System (INIS)

    Coulthard, I.; Antel, W. J. Jr.; Frigo, S. P.; Freeland, J. W.; Moore, J.; Calaway, W. S.; Pellin, M. J.; Mendelsohn, M.; Sham, T. K.; Naftel, S. J.

    2000-01-01

    Results of resonant Auger spectroscopy experimental are presented for Cu, Co, and oxidized Al. Sublifetime narrowing of Auger spectra and generation of sublifetime narrowed absorption spectra constructed from Auger yield measurements were observed. Resonant Auger yields are used to identify three chemical states of oxidized Al. Partial absorption yield spectra were derived giving detailed electronic information and thickness information for the various chemical states of the bulk metal, the passivating aluminum oxide layer, and the metal-oxide interface region. In addition, the total absorption yield spectrum for the oxidized Al sample was constructed from the partial yield data, supporting the consistency of our method. (c) 2000 American Vacuum Society

  5. [Study on the disposal process for removing heavy metal ions from wastewater by composite biosorbent of nano Fe3O4/Sphaerotilus natans].

    Science.gov (United States)

    Guan, Xiao-Hui; Qin, Yu-Chun; Wang, Li-Wen; Yin, Rong; Lu, Min; Yang, Ying-Jun

    2007-02-01

    Composite biosorbent nano Fe3O4/Sphaerotilus natans was prepared when nano Fe3O4 was used as carrier, then the composite biosorbent characterized by infrared instrument and investigated on adsorbing heavy metal ions from wastewater. Infrared spectrum analysis shows that--CONH--and--OH are principal activated groups of composite biosorbent. The experiment of adsorption shows that biomass concentration and flow velocity are main influencing factors. The composite biosorbent has best effect on the adsorption of Cu2+ under the conditions of biomass 1.5 g/L (Sphaerotilus natans/Fe3O4 = 3:2), flow velocity 0.96 L/h and initial concentration of Cu2+ was less than 20 mg/L. Composite biosorbent can be used for more 10 times when biosorbent was regenerated by HCl solution, and HCl solution can be used 3 times repeatedly. The selective sequence was Ph2+ > Cu2+ > Zn2+ > Cd2+.

  6. Changes in mobility and solubility of the redox sensitive metals Fe, Mn and Co at the seawater-sediment interface following CO2 seepage

    Directory of Open Access Journals (Sweden)

    E. Steinnes

    2010-02-01

    Full Text Available The impact of CO2 seepage on the solubility and distribution of the redox-sensitive metals iron, manganese, and cobalt in seawater and sediment pore water has been studied in experiments in laboratory-scale 0.6 m3 chambers. The mobility and solubility of Fe, Mn and Co were investigated in seawater, membrane filtered seawater, and DGT samplers deployed in water and sediment during a 26 day CO2 seepage study. During the first phase of the experiment of CO2 seepage (0–16 days, total acid-leachable (pH 1 and "dissolved" (<0.2 μm concentrations of Fe, Mn and Co (DFe, DMn and DCo in the seawater increased significantly; the ratios of concentrations of DFe, DMn and DCo in the CO2 chamber to the corresponding values in the control chamber (RDFe, RDMn and RDCo were as high as 6, 65 and 58, respectively. The second phase of experiment consisted of an additional 10 days of incubation, where the concentrations of all the metals studied still increased but at reduced rates for DMn and DCo. The highest values of RDFe, RDMn and RDCo were about 3 for all metals during this part of the experiment. DGT (diffusive gradients in thin film labile fractions denoted FeDGT, MnDGT and CoDGT were, respectively 50, 25 and 22 times higher in the CO2 seepage chamber than in the control chamber in the first phase of the experiment. During the second phase, all DGT labile metal concentrations still increased considerably, most notably for Fe. The ratio of FeDGT in the CO2 chamber to that in the control (RDGT-Fe was still high, about 5, in the second phase of the experiment, whereas the increase in MnDGT and CoDGT slowed down. Our results indicate that acidification following CO2 seepage enhances the mobility and solubility of Fe Mn and Co in sediment and overlying water with contribution of changing in redox conditions and seepage related re-suspension.

  7. The system Fe-Os-S at 1180°, 1100°and 900°C

    DEFF Research Database (Denmark)

    Karup-Møller, Sven; Makovicky, E.

    2002-01-01

    Phase relations in the condensed system Fe-Os-S were investigated by means of dry syntheses from the elements at 1180degrees, 1100degrees and 900degreesC. The Fe-rich sulfide melt dissolves only traces of Os. Fe1-xS dissolves up to 0.7 at.% Os at 1180degreesC; Os solubility decreases to 0.3 at...... partition coefficients for Os. The three-phase association alloy-FeS1-xS-OsS2 involves alloys with less than 1 at.% Fe. The solubility of Fe in OsS2 increases with decreasing temperature and increasing fugacity of sulfur, possibly making analyses of erlichmanite for trace quantities of Fe important....

  8. Highly selective removal of Hg2+ and Pb2+ by thiol-functionalized Fe3O4@metal-organic framework core-shell magnetic microspheres

    Science.gov (United States)

    Ke, Fei; Jiang, Jing; Li, Yizhi; Liang, Jing; Wan, Xiaochun; Ko, Sanghoon

    2017-08-01

    In this work, we report a novel type of thiol-functionalized magnetic core-shell metal-organic framework (MOF) microspheres that can be potentially used for selective removal of Hg2+ and Pb2+ in the presence of other background ions from wastewater. The monodisperse Fe3O4@Cu3(btc)2 core-shell magnetic microspheres have been fabricated by a versatile step-by-step assembly strategy. Further, the thiol-functionalized Fe3O4@Cu3(btc)2 magnetic microspheres were successfully synthesized by utilizing a facile postsynthetic strategy. Significantly, the thiol-functionalized Fe3O4@Cu3(btc)2 magnetic microspheres exhibit remarkably selective adsorption affinity for Hg2+ (Kd = 5.98 × 104 mL g-1) and Pb2+ (Kd = 1.23 × 104 mL g-1), while a weaker binding affinity occurred for the other background ions such as Ni2+, Na+, Mg2+, Ca2+, Zn2+ and Cd2+. The adsorption kinetics follow the pseudo-second-order rate equation and with an almost complete removal of Hg2+ and Pb2+ from the mixed heavy metal ions wastewater (0.5 mM) within 120 min. Moreover, this adsorbent can be easily recycled because of the presence of the magnetic Fe3O4 core. This work provides a promising functionalized porous magnetic Fe3O4@MOF-based adsorbent with easy recycling property for the selective removal of heavy metal ions from wastewater.

  9. Corrosion behavior of Al-Fe-sputtering-coated steel, high chromium steels, refractory metals and ceramics in high temperature Pb-Bi

    International Nuclear Information System (INIS)

    Abu Khalid, Rivai; Minoru, Takahashi

    2007-01-01

    Corrosion tests of Al-Fe-coated steel, high chromium steels, refractory metals and ceramics were carried out in high temperature Pb-Bi at 700 C degrees. Oxygen concentrations in this experiment were 6.8*10 -7 wt.% for Al-Fe-coated steels and 5*10 -6 wt.% for high chromium steels, refractory metals and ceramics. All specimens were immersed in molten Pb-Bi in a corrosion test pot for 1.000 hours. Coating was done with using the unbalanced magnetron sputtering (UBMS) technique to protect the steel from corrosion. Sputtering targets were Al and SUS-304. Al-Fe alloy was coated on STBA26 samples. The Al-Fe alloy-coated layer could be a good protection layer on the surface of steel. The whole of the Al-Fe-coated layer still remained on the base surface of specimen. No penetration of Pb-Bi into this layer and the matrix of the specimen. For high chromium steels i.e. SUS430 and Recloy10, the oxide layer formed in the early time could not prevent the penetration of Pb-Bi into the base of the steels. Refractory metals of tungsten (W) and molybdenum (Mo) had high corrosion resistance with no penetration of Pb-Bi into their matrix. Penetration of Pb-Bi into the matrix of niobium (Nb) was observed. Ceramic materials were SiC and Ti 3 SiC 2 . The ceramic materials of SiC and Ti 3 SiC 2 had high corrosion resistance with no penetration of Pb-Bi into their matrix. (authors)

  10. Metal cation exchange reactions of ore minerals in Fe-Mn crusts of the Marcus Wake Rise (Pacific Ocean) in aqueous-salt solutions

    Science.gov (United States)

    Novikov, G. V.; Bogdanova, O. Yu.; Melnikov, M. E.; Drozdova, A. N.; Lobus, N. V.; Shulga, N. A.

    2017-12-01

    It is shown that the reaction ability of metal cations of ore minerals in Fe-Mn crusts of the Marcus Wake Rise increases in the following manner: (Co2+ minerals is constant and includes these metal cations. Ca2+ and Na+ are major contributors to the exchange capacity of the ore minerals. The capacity of the ore minerals by cations of alkali and base metals is 0.43-0.60 and 2.08-2.70 mg-equiv/g, respectively. The exchange capacity of the ore minerals by cations of base metals increases linearly with the increase in the MnO2 content of the crust and does not depend on the geographical locations of the Marcus Wake guyots.

  11. Effect of heavy-metal insertions at Fe/MgO interfaces on electric-field-induced modification of magnetocrystalline anisotropy

    Energy Technology Data Exchange (ETDEWEB)

    Nakamura, K.; Nomura, T. [Department of Physics Engineering, Mie University, Tsu, Mie 514-8507 (Japan); Pradipto, A.-M. [Department of Physics Engineering, Mie University, Tsu, Mie 514-8507 (Japan); Institute for Chemical Research, Kyoto University, Uji, Kyoto 611-0011 (Japan); Nawa, K.; Akiyama, T.; Ito, T. [Department of Physics Engineering, Mie University, Tsu, Mie 514-8507 (Japan)

    2017-05-01

    Magnetocrystalline anisotropy (MCA) at Fe/MgO interfaces with insertions of 3d (Co, Ni), 4d (Ru, Rh, Pd), and 5d (Os, Ir, Pt) elements in external electric fields was investigated from first-principles calculations. The MCA energy and the electric-field-induced MCA modification dramatically depend on the inserted elements. Large MCA modification may be achieved by heavy-metal insertions, in which the strength of spin-orbit coupling of inserted elements and the position of the Fermi level relative to d band level play key roles. - Highlights: • MCA at Fe/MgO interface dramatically depends on insertions of 3d, 4d, and 5d elements. • Large electric-field-induced MCA modification is achieved by heavy-metal insertions. • Position of Fermi level relative to d band level plays key role in determining MCA.

  12. Variation in band gap of lanthanum chromate by transition metals doping LaCr0.9A0.1O3 (A:Fe/Co/Ni)

    International Nuclear Information System (INIS)

    Naseem, Swaleha; Khan, Wasi; Saad, A. A.; Shoeb, M.; Ahmed, Hilal; Naqvi, A. H.; Husain, Shahid

    2014-01-01

    Transition metal (Fe, Co, Ni) doped lanthanum chromate (LaCrO 3 ) nanoparticles (NPs) were prepared by gel combustion method and calcinated at 800°C. Microstructural studies were carried by XRD and SEM/EDS techniques. The results of structural characterization show the formation of all samples in single phase without any impurity. Optical properties were studied by UV- visible and photoluminescence techniques. The energy band gap was calculated and the variation was observed with the doping of transition metal ions. Photoluminescence spectra show the emission peak maxima for the pure LaCrO 3 at about 315 nm. Influence of Fe, Co, Ni doping was studied and compared with pure lanthanum chromate nanoparticles

  13. New lithium metal polymer solid state battery for an ultrahigh energy: nano C-LiFePO₄ versus nano Li1.2V₃O₈.

    Science.gov (United States)

    Hovington, P; Lagacé, M; Guerfi, A; Bouchard, P; Mauger, A; Julien, C M; Armand, M; Zaghib, K

    2015-04-08

    Novel lithium metal polymer solid state batteries with nano C-LiFePO4 and nano Li1.2V3O8 counter-electrodes (average particle size 200 nm) were studied for the first time by in situ SEM and impedance during cycling. The kinetics of Li-motion during cycling is analyzed self-consistently together with the electrochemical properties. We show that the cycling life of the nano Li1.2V3O8 is limited by the dissolution of the vanadium in the electrolyte, which explains the choice of nano C-LiFePO4 (1300 cycles at 100% DOD): with this olivine, no dissolution is observed. In combination with lithium metal, at high loading and with a stable SEI an ultrahigh energy density battery was thus newly developed in our laboratory.

  14. Metal Doping Effect of the M-Co2P/Nitrogen-Doped Carbon Nanotubes (M = Fe, Ni, Cu) Hydrogen Evolution Hybrid Catalysts.

    Science.gov (United States)

    Pan, Yuan; Liu, Yunqi; Lin, Yan; Liu, Chenguang

    2016-06-08

    The enhancement of catalytic performance of cobalt phosphide-based catalysts for the hydrogen evolution reaction (HER) is still challenging. In this work, the doping effect of some transition metal (M = Fe, Ni, Cu) on the electrocatalytic performance of the M-Co2P/NCNTs (NCNTs, nitrogen-doped carbon nanotubes) hybrid catalysts for the HER was studied systematically. The M-Co2P/NCNTs hybrid catalysts were synthesized via a simple in situ thermal decomposition process. A series of techniques, including X-ray diffraction, X-ray photoelectron spectroscopy, inductively coupled plasma-optical emission spectrometry, transmission electron microscopy, and N2 sorption were used to characterize the as-synthesized M-Co2P/NCNTs hybrid catalysts. Electrochemical measurements showed the catalytic performance according to the following order of Fe-Co2P/NCNTs > Ni-Co2P/NCNTs > Cu-Co2P/NCNTs, which can be ascribed to the difference of structure, morphology, and electronic property after doping. The doping of Fe atoms promote the growth of the [111] crystal plane, resulting in a large specific area and exposing more catalytic active sites. Meanwhile, the Fe(δ+) has the highest positive charge among all the M-Co2P/NCNTs hybrid catalysts after doping. All these changes can be used to contribute the highest electrocatalytic activity of the Fe-Co2P/NCNTs hybrid catalyst for HER. Furthermore, an optimal HER electrocatalytic activity was obtained by adjusting the doping ratio of Fe atoms. Our current research indicates that the doping of metal is also an important strategy to improve the electrocatalytic activity for the HER.

  15. Preparation and properties of Fe{sub 80−x}Ni{sub x}P{sub 14}B{sub 6} bulk metallic glasses

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Ling; Ma, XiuHua [School of Physics Science and Technology, Xinjiang University, Urumqi, Xinjiang 830046 (China); Li, Qiang, E-mail: qli@xju.edu.cn [School of Physics Science and Technology, Xinjiang University, Urumqi, Xinjiang 830046 (China); Zhang, Jijun [School of Physics Science and Technology, Xinjiang University, Urumqi, Xinjiang 830046 (China); Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo, Zhejiang 315201 (China); Dong, Yaqiang; Chang, Chuntao [Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo, Zhejiang 315201 (China)

    2014-09-01

    Highlights: • Fe{sub 80−x}Ni{sub x}P{sub 14}B{sub 6} (x = 20–50 at.%) BMGs were prepared by fluxing and J-quenching techniques. • The highest GFA is reached at x = 40 and the corresponding critical diameter is up to 2.5 mm. • The present FeNi-based BMGs exhibit very large ε{sub p} and the ε{sub p} of Fe{sub 30}Ni{sub 50}P{sub 14}B{sub 6} BMG is 11.7%. • The present FeNi-based BMGs have much higher corrosion resistance than stainless steel. - Abstract: Bulk Fe{sub 80−x}Ni{sub x}P{sub 14}B{sub 6} (x = 20, 30, 40, 50 at.%) glassy alloy rods with the diameters of 1.0–2.5 mm were synthesized by combining fluxing technique and J-quenching technique. The glassy alloy rods were characterized by X-ray diffraction (XRD), differential scanning calorimetry (DSC) and vibrating sample magnetometer (VSM). It is found that the range of supercooled liquid region (ΔT{sub x}) is 27–32 K. The saturation magnetization of Fe{sub 80−x}Ni{sub x}P{sub 14}B{sub 6} (x = 20, 30, 40, 50 at.%) bulk glassy alloys gradually decreases from 1.13 T to 0.58 T with increasing Ni content from x = 20 to x = 50. More importantly, the present quaternary FeNiPB bulk metallic glasses (BMGs) shows a significant plastic strain, in particular, the plastic strain of Fe{sub 30}Ni{sub 50}P{sub 14}B{sub 6} BMG reaches as high as 11.7%. The corrosion resistance of the present FeNiPB BMGs was studied by weight-loss method, potentiodynamic polarization curves and scanning electron microscopy (SEM). It is shown that the corrosion resistance of the present FeNiPB BMGs in 0.5 M NaCl and 1 M HCl solution increases with Ni content, and further the present FeNiPB BMGs exhibit larger E{sub corr} values and lower I{sub corr} values, i.e. higher corrosion resistances, than that of stainless steel.

  16. Some histological and histochemical observations on the transfer of two metals (Fe/sup 3 +/, Cu/sup 2 +/) in Lymnaea (galba) Truncatula muller

    Energy Technology Data Exchange (ETDEWEB)

    Rondelaud, D.; Chaisemartin, C.; Barthe, D.

    1976-01-01

    The transfer processes of iron and copper in Lymnaea trunculate were examined by histochemical, histopathologic, and quantitative tests of Fe/sup 3/+ and Cu/sup 2 +/ in the soft tissues. Iron penetrated the peritentacular areas and the alimentary canal. This metal was excreted by dense cytoplasm cells of the digestive gland and by ovules of the genital gland. Peritentacular areas were solely responsible for copper penetration. This metal was carried by amibocytes and excreted in granules elaborated by digestive cells of the digestive gland.

  17. Thermodynamic Constraints in Using AuM (M = Fe, Co, Ni, and Mo) Alloys as N₂ Dissociation Catalysts: Functionalizing a Plasmon-Active Metal.

    Science.gov (United States)

    Martirez, John Mark P; Carter, Emily A

    2016-02-23

    The Haber-Bosch process for NH3 synthesis is arguably one of the greatest inventions of the 20th century, with a massive footprint in agriculture and, historically, warfare. Current catalysts for this reaction use Fe for N2 activation, conducted at high temperatures and pressures to improve conversion rate and efficiency. A recent finding shows that plasmonic metal nanoparticles can either generate highly reactive electrons and holes or induce resonant surface excitations through plasmonic decay, which catalyze dissociation and redox reactions under mild conditions. It is therefore appealing to consider AuM (M = Fe, Co, Ni, and Mo) alloys to combine the strongly plasmonic nature of Au and the catalytic nature of M metals toward N2 dissociation, which together might facilitate ammonia production. To this end, through density functional theory, we (i) explore the feasibility of forming these surface alloys, (ii) find a pathway that may stabilize/deactivate surface M substituents during fabrication, and (iii) define a complementary route to reactivate them under operational conditions. Finally, we evaluate their reactivity toward N2, as well as their ability to support a pathway for N2 dissociation with a low thermodynamic barrier. We find that AuFe possesses similar appealing qualities, including relative stability with respect to phase separation, reversibility of Fe oxidation and reduction, and reactivity toward N2. While AuMo achieves the best affinity toward N2, its strong propensity toward oxidation could greatly limit its use.

  18. The ternary Fe-C-N system: Homogeneous distributions of nitrogen and carbon

    DEFF Research Database (Denmark)

    Brink, Bastian; Ståhl, Kenny; Christiansen, Thomas Lundin

    2017-01-01

    of the nitriding and carburizing potentials, tailored nitrogen and carbon contents can be achieved, which allows assessment of a phase stability diagram for the Fe-N-C system, for which available experimental data is limited. Thermal decomposition sequences were established for the various iron carbides and (carbo...

  19. Degradation of EDTA-Fe solutions using a combined AOP-biological system

    Energy Technology Data Exchange (ETDEWEB)

    Gomez, C.; Freer, J.; Lizama, C.; Mansilla, H.D. [Lab. de Recursos Renovables, Facultad de Ciencias Quimicas, Univ. de Concepcion, Concepcion (Chile); Rodriguez, J. [Lab. de Recursos Renovables, Facultad de Ciencias Forestales, Univ. de Concepcion, Concepcion (Chile)

    2003-07-01

    Degradation of 2.5 x 10{sup -3} M EDTA-Fe solutions was performed in a coupled photocatalytic-biological reactor. The system consists of a photochemical annular reactor filled with TiO{sub 2} immobilized on glass Raschig rings coupled with an activated sludge continuous reactor. Around 50% of EDTA degradation were reached after 150 min irradiation. Simultaneously a four-time increase in the biodegradability, measured as BOD{sub 5}/COD ratio, was observed. The activated sludge is not capable to degrade the complex EDTA-Fe but remove partially the COD and efficiently the BOD{sub 5} of the photochemical treated solution. (orig.)

  20. Power Management of Hybrid Power Systems with Li-Fe Batteries and Supercapacitors for Mobile Robots

    OpenAIRE

    Guohui Wang; Zhiquan Dai; Yong Guan; Pengfei Dong; Lifeng Wu

    2014-01-01

    This paper presents an energy management strategy of a Li-Fe battery and supercapacitor hybrid power system to provide both high power density and energy density for mobile robots with fluctuating workloads. A two-phase power-optimization approach is proposed to exploit the high power density of supercapacitors and the high energy density of Li-Fe batteries. With our strategy, large peak power can be provided for a short time period whenever needed, while low power can be provided for very lo...

  1. Structural and magnetic properties of FeCoC system obtained by mechanical alloying

    Energy Technology Data Exchange (ETDEWEB)

    Rincón Soler, A. I. [Universidad Tecnológica de Pereira, Fac. de Ciencias, Depto. de Física (Colombia); Rodríguez Jacobo, R. R., E-mail: rrrodriguez@uao.edu.co [Universidad Autónoma de Occidente, Fac. de Ciencias Básicas, Depto. de Física (Colombia); Medina Barreto, M. H.; Cruz-Muñoz, B. [Universidad Tecnológica de Pereira, Fac. de Ciencias, Depto. de Física (Colombia)

    2017-11-15

    Fe{sub 96−X}Co{sub X}C{sub 4} (x = 0, 10, 20, 30, 40 at. %) alloys were obtained by mechanical alloying of Fe, C and Co powders using high-energy milling. The structural and magnetic properties of the alloy system were analyzed by X-ray diffraction, Scanning Electron Microscopy (SEM), Vibrating Sample Magnetometer (VSM) and Mössbauer Spectrometry at room temperature. The X-ray diffraction patterns showed a BCC-FeCoC structure phase for all samples, as well as a lattice parameter that slightly decreases with Co content. The saturation magnetization and coercive field were analyzed as a function of Co content. The Mössbauer spectra were fitted with a hyperfine magnetic field distribution showing the ferromagnetic behavior and the disordered character of the samples. The mean hyperfine magnetic field remained nearly constant (358 T) with Co content.

  2. Structural and magnetic properties of FeCoC system obtained by mechanical alloying

    International Nuclear Information System (INIS)

    Rincón Soler, A. I.; Rodríguez Jacobo, R. R.; Medina Barreto, M. H.; Cruz-Muñoz, B.

    2017-01-01

    Fe 96−X Co X C 4 (x = 0, 10, 20, 30, 40 at. %) alloys were obtained by mechanical alloying of Fe, C and Co powders using high-energy milling. The structural and magnetic properties of the alloy system were analyzed by X-ray diffraction, Scanning Electron Microscopy (SEM), Vibrating Sample Magnetometer (VSM) and Mössbauer Spectrometry at room temperature. The X-ray diffraction patterns showed a BCC-FeCoC structure phase for all samples, as well as a lattice parameter that slightly decreases with Co content. The saturation magnetization and coercive field were analyzed as a function of Co content. The Mössbauer spectra were fitted with a hyperfine magnetic field distribution showing the ferromagnetic behavior and the disordered character of the samples. The mean hyperfine magnetic field remained nearly constant (358 T) with Co content.

  3. Environmentally Benign Tribo-systems for Metal Forming

    DEFF Research Database (Denmark)

    Bay, Niels; Azushima, A.; Groche, P.

    2010-01-01

    The growing awareness of environmental issues and the requirements to establish solutions diminishing the impact on working environment as well as external environment has initiated ever increasing efforts to develop new, environmentally benign tribological systems for metal forming. The present ...

  4. Synthesis of MnFe2O4@Mn-Co oxide core-shell nanoparticles and their excellent performance for heavy metal removal.

    Science.gov (United States)

    Ma, Zichuan; Zhao, Dongyuan; Chang, Yongfang; Xing, Shengtao; Wu, Yinsu; Gao, Yuanzhe

    2013-10-21

    Magnetic nanomaterials that can be easily separated and recycled due to their magnetic properties have received considerable attention in the field of water treatment. However, these nanomaterials usually tend to aggregate and alter their properties. Herein, we report an economical and environmentally friendly method for the synthesis of magnetic nanoparticles with core-shell structure. MnFe2O4 nanoparticles have been successfully coated with amorphous Mn-Co oxide shells. The synthesized MnFe2O4@Mn-Co oxide nanoparticles have highly negatively charged surface in aqueous solution over a wide pH range, thus preventing their aggregation and enhancing their performance for heavy metal cation removal. The adsorption isotherms are well fitted to a Langmuir adsorption model, and the maximal adsorption capacities of Pb(II), Cu(II) and Cd(II) on MnFe2O4@Mn-Co oxide are 481.2, 386.2 and 345.5 mg g(-1), respectively. All the metal ions can be completely removed from the mixed metal ion solutions in a short time. Desorption studies confirm that the adsorbent can be effectively regenerated and reused.

  5. Trichloroethylene oxidation performance in sodium percarbonate (SPC)/Fe2+ system.

    Science.gov (United States)

    Zang, Xueke; Gu, Xiaogang; Lu, Shuguang; Qiu, Zhaofu; Sui, Qian; Lin, Kuangfei; Du, Xiaoming

    2014-01-01

    In this study, in-situ chemical oxidation technique employing Fe(II) catalytic sodium percarbonate (SPC) to stimulate the oxidation of trichloroethylene (TCE) in contaminated groundwater remediation was investigated. The effects of various factors including the SPC/TCE/Fe2+ molar ratio, the initial solution pH and the widely found constituents in groundwater matrix such as Cl(-), HCO3(-), SO4(2-) and NO3(-) anions and natural organic matters were evaluated. The experimental results showed that TCE could be completely oxidized in 5 min at 20 degrees C with a SPC/TCE/Fe2+ molar ratio of 5:1:10, indicating the significant effectiveness of the SPC/Fe2+ system for TCE removal. The initial solution pH value (from 3 to 11) has less influence on TCE oxidation rate. In contrast, Cl(-) and HCO3(-) anions had a negative effect on TCE removal in which HCO3(-) possesses a stronger influence than Cl(-), whereas the effects of both SO4(2-) and NO3(-) anions appeared to be negligible. With the 1.0-10 mg/L concentrations of humic acid in solution, slightly inhibitive effect was observed, suggesting that dissolved organic matters consumed less SPC and had a negligible effect on the oxidation of TCE in SPC/Fe2+ system. From the intermediate products' analyses and the released Cl(-) contents from TCE parent contaminant in solution, all the decomposed TCE had completely dechlorinated and led to carbon dioxide and hydrocarbon. In conclusion, Fe(II) catalytic SPC oxidation is a highly promising technique for TCE-contaminated groundwater remediation, but some complex constituents such as HCO3(-), in in-situ groundwater matrix should be carefully considered for its practical application.

  6. The delicate electronic and magnetic structure of the LaFePnO system (Pn = pnicogen)

    Energy Technology Data Exchange (ETDEWEB)

    Lebegue, S [Laboratoire de Cristallographie et de Modelisation des Materiaux Mineraux et Biologiques, UMR 7036, CNRS-Universite Henri Poincare, BP 239, F-54506 Vandoeuvre-les-Nancy (France); Yin, Z P; Pickett, W E [Department of Physics, University of California Davis, Davis, CA 95616 (United States)], E-mail: sebastien.lebegue@lcm3b.uhp-nancy.fr

    2009-02-15

    The occurrence of high-temperature superconductivity, and the competition with magnetism, in stoichiometric and doped LaFeAsO and isostructural iron oxypnictides is raising many fundamental questions about the electronic structure and magnetic interactions in this class of materials. There are now sufficient experimental data that it may be possible to identify the important issues whose resolution will lead to the understanding of this system. In this paper, we address a number of the important issues. One important characteristic is the Fe-As distance (or more abstractly the pnicogen (Pn) height z(Pn)); we present results for the effect of z(Pn) on the electronic structure, energetics and Fe magnetic moment. We also study LaFeAsO under pressure, and investigate the effects of both electron and hole doping within the virtual crystal approximation. The electric field gradients for all atoms in the LaFeAsO compound are presented (undoped and doped) and compared with available data. The observed ({pi}, {pi}, {pi}) magnetic order is studied and compared with the computationally simpler ({pi}, {pi}, 0) order which is probably a very good model in most respects. We investigate the crucial role of the pnicogen atom in this class, and predict the structures and properties of the N and Sb counterparts that have not yet been reported experimentally. At a certain volume a gap opens at the Fermi level in LaFeNO, separating bonding from antibonding bands. This is the first evidence that this class of materials indeed has an underlying semimetallic character, and this separation suggests directions for a better simple understanding of the seemingly intricate electronic structure of this system. Finally, we address briefly differences resulting from substitution of post-lanthanum rare earth atoms, which have been observed to enhance the superconducting critical temperature substantially.

  7. The tripeptide feG ameliorates systemic inflammatory responses to rat intestinal anaphylaxis

    Directory of Open Access Journals (Sweden)

    Davison Joseph S

    2002-08-01

    Full Text Available Abstract Background Food allergies are generally associated with gastrointestinal upset, but in many patients systemic reactions occur. However, the systemic effects of food allergies are poorly understood in experimental animals, which also offer the opportunity to explore the actions of anti-allergic drugs. The tripeptide D-phenylalanine-D-glutamate-Glycine (feG, which potentially alleviates the symptoms of systemic anaphylactic reactions, was tested to determine if it also reduced systemic inflammatory responses provoked by a gastric allergic reaction. Results Optimal inhibition of intestinal anaphylaxis was obtained when 100 μg/kg of feG was given 20 min before the rats were challenged with antigen. The increase in total circulating neutrophils and accumulation of neutrophils in the heart, developing 3 h and 24 h, respectively, after antigen challenge were reduced by both feG and dexamethasone. Both anti-inflammatory agents reduced the increase in vascular permeability induced by antigen in the intestine and the peripheral skin (pinna, albeit with different time courses. Dexamethasone prevented increases in vascular permeability when given 12 h before antigen challenge, whereas feG was effective when given 20 min before ingestion of antigen. The tripeptide prevented the anaphylaxis induced up regulation of specific antibody binding of a cell adhesion molecule related to neutrophil activation, namely CD49d (α4 integrin. Conclusions Aside from showing that intestinal anaphylaxis produces significant systemic inflammatory responses in non-intestinal tissues, our results indicate that the tripeptide feG is a potent inhibitor of extra-gastrointestinal allergic reactions preventing both acute (30 min and chronic (3 h or greater inflammatory responses.

  8. Effect of Fe substitution on the structural, magnetic and electron-transport properties of half-metallic Co2TiSi

    Science.gov (United States)

    Jin, Y.; Waybright, J.; Kharel, P.; Tutic, I.; Herran, J.; Lukashev, P.; Valloppilly, S.; Sellmyer, D. J.

    2017-05-01

    The structural, magnetic and electron-transport properties of Co2Ti1-xFexSi (x = 0, 0.25, 0.5) ribbons prepared by arc-melting and melt-spinning were investigated. The rapidly quenched Co2Ti0.5Fe0.5Si crystallized in the cubic L21 structure whereas Co2Ti0.75Fe0.25Si and Co2TiFe0Si showed various degrees of B2-type disorder. At room temperature, all the samples are ferromagnetic, and the Curie temperature increased from 360 K for Co2TiSi to about 800 K for Co2Ti0.5Fe0.5Si. The measured magnetization also increased due to partial substitution of Fe for Ti atoms. The ribbons are moderately conducting and show positive temperature coefficient of resistivity with the room temperature resistivity being between 360 μ Ω cm and 440 μ Ω cm . The experimentally observed structural and magnetic properties are consistent with the results of first-principle calculations. Our calculations also indicate that the Co2Ti1-xFexSi compound remains nearly half-metallic for x ≤ 0.5. The predicted large band gaps and high Curie temperatures much above room temperature make these materials promising for room temperature spintronic and magnetic applications.

  9. CoFe2O4 derived-from bi-metal organic frameworks wrapped with graphene nanosheets as advanced anode for high-performance lithium ion batteries

    Science.gov (United States)

    Yang, Hongxun; Zhang, Kaixuan; Wang, Yang; Yan, Chao; Lin, Shengling

    2018-04-01

    CoFe2O4/graphene nanosheets (GNS) nanocomposites derived from bi-metal organic frameworks and graphene oxides were firstly synthesized via a facile one-pot chemical precipitation with subsequent thermal decomposition method. The as-prepared CoFe2O4/GNS were characterized by XRD, Raman, SEM, TEM and BET adsorption-desorption. As an anode for lithium ion batteries, the CoFe2O4/GNS nanocomposites exhibited an obvious enhancement electrochemical property in terms of a higher discharge capacity of 1061.7 mAh g-1 after 100 cycles at 100 mA g-1 with 75.1% capacity retention and the excellent reversible capacity of 956.2 mAh g-1 when the charge-discharge rate returned from 2 A g-1 to 0.1 A g-1 after 60 cycles. This enhancement could be attributed to the synergistic effects between Co and Fe oxides, and the graphene nanosheets which could not only accommodate the volume variations of CoFe2O4 nanoparticles during cycling, but also improve the contact area between electrolyte and electrodes.

  10. Robust Fe3Mo3C Supported IrMn Clusters as Highly Efficient Bifunctional Air Electrode for Metal-Air Battery.

    Science.gov (United States)

    Cui, Zhiming; Li, Yutao; Fu, Gengtao; Li, Xiang; Goodenough, John B

    2017-10-01

    Catalysts at the air cathode for oxygen reduction and evolution reactions are central to the stability of rechargeable metal-air batteries, an issue that is gaining increasing interest in recent years. Herein, a highly durable and efficient carbide-based bifunctional catalyst consisting of iron-molybdenum carbide (Fe 3 Mo 3 C) and IrMn nanoalloys is demonstratred. This carbide is chemically stable in alkaline media and over the potential range of an air cathode. More importantly, Fe 3 Mo 3 C is very active for oxygen reduction reaction (ORR) in alkaline media. Fe 3 Mo 3 C supported IrMn as a bifunictional catalysts exhibits superior catalytic performance than the state of the art ORR catalyst (Pt/C) and the oxygen evolution reaction catalyst (Ir/C). IrMn/Fe 3 Mo 3 C enables Zn-air batteries to achieve long-term cycling performance over 200 h with high efficiency. The extraordinarily high performance of IrMn/Fe 3 Mo 3 C bifunictional catalyst provides a very promising alternative to the conventional Pt/C and Ir/C catalyst for an air cathode in alkaline electrolyte. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  11. Development of readout system for FE-I4 pixel module using SiTCP

    Science.gov (United States)

    Teoh, J. J.; Hanagaki, K.; Ikegami, Y.; Takubo, Y.; Terada, S.; Unno, Y.

    2013-12-01

    The ATLAS pixel detector will be replaced in the future High Luminosity-Large Hadron Collider (HL-LHC) upgrade to preserve or improve the detector performance at high luminosity environment. To meet the tight requirements of the upgrade, a new pixel Front-End (FE) Integrated Circuit (IC) called FE-I4 has been developed. We have then devised a readout system for the new FE IC. Our system incorporates Silicon Transmission Control Protocol (SiTCP) technology (Uchida, 2008 [1]) which utilizes the standard TCP/IP and UDP communication protocols. This technology allows direct data access and transfer between a readout hardware chain and PC via a high speed Ethernet. In addition, the communication protocols are small enough to be implemented in a single Field-Programable Gate Array (FPGA). Relying on this technology, we have been able to construct a very compact, versatile and fast readout system. We have developed a firmware and software together with the readout hardware chain. We also have established basic functionalities for reading out FE-I4.

  12. Design of template-stabilized active and earth-abundant oxygen evolution catalysts in acid† †Electronic supplementary information (ESI) available: CVs for unary metal oxides deposition, electrochemical stability at higher current densities for unary metal oxides at pH 2.5, EDS maps for CoMnOx and CoPbOx, STEM images and PXRD of CoMnOx and CoFePbOx, high-resolution XPS of Fe 2p for CoFePbOx, Pourbaix diagrams (of Mn, Co, Pb, and Fe), and elemental analysis. See DOI: 10.1039/c7sc01239j Click here for additional data file.

    Science.gov (United States)

    Huynh, Michael; Ozel, Tuncay; Liu, Chong; Lau, Eric C.

    2017-01-01

    Oxygen evolution reaction (OER) catalysts that are earth-abundant and are active and stable in acid are unknown. Active catalysts derived from Co and Ni oxides dissolve at low pH, whereas acid stable systems such as Mn oxides (MnOx) display poor OER activity. We now demonstrate a rational approach for the design of earth-abundant catalysts that are stable and active in acid by treating activity and stability as decoupled elements of mixed metal oxides. Manganese serves as a stabilizing structural element for catalytically active Co centers in CoMnOx films. In acidic solutions (pH 2.5), CoMnOx exhibits the OER activity of electrodeposited Co oxide (CoOx) with a Tafel slope of 70–80 mV per decade while also retaining the long-term acid stability of MnOx films for OER at 0.1 mA cm–2. Driving OER at greater current densities in this system is not viable because at high anodic potentials, Mn oxides convert to and dissolve as permanganate. However, by exploiting the decoupled design of the catalyst, the stabilizing structural element may be optimized independently of the Co active sites. By screening potential–pH diagrams, we replaced Mn with Pb to prepare CoFePbOx films that maintained the high OER activity of CoOx at pH 2.5 while exhibiting long-term acid stability at higher current densities (at 1 mA cm–2 for over 50 h at pH 2.0). Under these acidic conditions, CoFePbOx exhibits OER activity that approaches noble metal oxides, thus establishing the viability of decoupling functionality in mixed metal catalysts for designing active, acid-stable, and earth-abundant OER catalysts. PMID:29163926

  13. System and method for producing metallic iron

    Science.gov (United States)

    Englund, David J.; Schlichting, Mark; Meehan, John; Crouch, Jeremiah; Wilson, Logan

    2014-07-29

    A method of production of metallic iron nodules comprises assembling a hearth furnace having a moveable hearth comprising refractory material and having a conversion zone and a fusion zone, providing a hearth material layer comprising carbonaceous material on the refractory material, providing a layer of reducible material comprising and iron bearing material arranged in discrete portions over at least a portion of the hearth material layer, delivering oxygen gas into the hearth furnace to a ratio of at least 0.8:1 ponds of oxygen to pounds of iron in the reducible material to heat the conversion zone to a temperature sufficient to at least partially reduce the reducible material and to heat the fusion zone to a temperature sufficient to at least partially reduce the reducible material, and heating the reducible material to form one or more metallic iron nodules and slag.

  14. Experimental Investigation and Thermodynamic Modeling of the B2O3-FeO-Fe2O3-Nd2O3 System for Recycling of NdFeB Magnet Scrap

    Science.gov (United States)

    Jakobsson, Lars Klemet; Tranell, Gabriella; Jung, In-Ho

    2017-02-01

    NdFeB magnet scrap is an alternative source of neodymium that could have a significantly lower impact on the environment than current mining and extraction processes. Neodymium can be readily oxidized in the presence of oxygen, which makes it easy to recover neodymium in oxide form. Thermochemical data and phase diagrams for neodymium oxide containing systems is, however, very limited. Thermodynamic modeling of the B2O3-FeO-Fe2O3-Nd2O3 system was hence performed to obtain accurate phase diagrams and thermochemical properties of the system. Key phase diagram experiments were also carried out for the FeO-Nd2O3 system in saturation with iron to improve the accuracy of the present modeling. The modified quasichemical model was used to describe the Gibbs energy of the liquid oxide phase. The Gibbs energy functions of the liquid phase and the solids were optimized to reproduce all available and reliable phase diagram data, and thermochemical properties of the system. Finally the optimized database was applied to calculate conditions for selective oxidation of neodymium from NdFeB magnet waste.

  15. Ion microprobe analyses of carbon in Fe-Ni metal in iron meteorites and mesosiderites

    Science.gov (United States)

    Goldstein, Joseph I.; Huss, Gary R.; Scott, Edward R. D.

    2017-03-01

    Carbon concentrations in kamacite, taenite, and plessite (kamacite-taenite intergrowths) were measured in 18 iron meteorites and 2 mesosiderites using the Cameca ims 1280 ion microprobe at the University of Hawai'i with a 5-7 μm beam and a detection limit of metal phases and other carbon-bearing minerals (graphite, haxonite, cohenite) in various meteorite groups. Carbon concentrations range from ∼100 to ∼1000 ppm in taenite and plessite in groups IAB, IIICD, and IIIAB, which contain graphite and/or carbides, but only 2-6 ppm in groups IVA, IVB and the ungrouped iron, Tishomingo, which lack graphite and carbides. Carbon contents in kamacite range from ∼2 to ∼10 ppm in most studied meteorites, including IIAB, but higher abundances were found in kamacite from IAB Pitts subgroup meteorites Pitts and Woodbine (12-15 ppm). Our carbon abundances for kamacite are lower than most published ion probe data, indicating that earlier carbon measurements had contamination problems. Grains of taenite and fine-grained plessite in carbon-rich meteorites, which all have normal M-shaped nickel profiles due to slow cooling, have diverse carbon contents and zoning profiles. This is because taenite decomposed by diverse mechanisms over a range of temperatures, when nickel could only diffuse over sub-μm distances. Carbon diffusion through taenite to growing carbides was rapid at the upper end of this temperature range, but was very limited at the lower end of the temperature range. In mesosiderites, carbon increases from 12 ppm in tetrataenite to 40-115 ppm in cloudy taenite as nickel decreases from 50% to 35%. Low carbon levels in tetrataenite may reflect ordering of iron and nickel; higher carbon in cloudy taenite is attributed to metastable bcc phase, possibly martensite, with ∼300 ppm carbon intergrown with tetrataenite. Pearlitic plessite, which only forms in carbon-rich irons, contains much less carbon than martensitic plessite: 10-20 ppm and 300-500, respectively, in

  16. One-Step Carbon Coating and Polyacrylamide Functionalization of Fe3O4 Nanoparticles for Enhancing Magnetic Adsorptive-Remediation of Heavy Metals

    Directory of Open Access Journals (Sweden)

    Mohamed A. Habila

    2017-11-01

    Full Text Available Magnetic nanoparticles are used in adsorptive removal of heavy metals from polluted wastewater. However, their poor stability in an acidic medium necessitates their protection with a coating layer. Coating magnetic nanoparticles with carbon showed proper protection but the heavy metal removal efficiency was slightly weak. However, to boost the removal efficiencies of surface functionalization, polyacrylamide was applied to carbon-coated Fe3O4 nanoparticles. In this paper, to facilitate the synthesis process, one-step carbon coating and polyacrylamide functionalization were conducted using the hydrothermal technique with the aim of enhancing the adsorptive removal capacity of Fe3O4 nanoparticles towards some heavy metals such as Cu(II, Ni(II, Co(II, and Cd(II. The results showed that the one-step process succeeded in developing a carbon coating layer and polyacrylamide functionality on Fe3O4 nanoparticles. The stability of the magnetic Fe3O4 nanoparticles as an adsorbent in an acidic medium was improved due to its resistance to the dissolution that was gained during carbon coating and surface functionalization with polyacrylamide. The adsorptive removal process was investigated in relation to various parameters such as pH, time of contact, metal ion concentrations, adsorbent dose, and temperature. The polyacrylamide functionalized Fe3O4 showed an improvement in the adsorption capacity as compared with the unfunctionalized one. The conditions for superior adsorption were obtained at pH 6; time of contact, 90 min; metal solution concentration, 200 mg/L; adsorbent dose, 0.3 g/L. The modeling of the adsorption data was found to be consistent with the pseudo-second-order kinetic model, which suggests a fast adsorption process. However, the equilibrium data modeling was consistent with both the Langmuir and Freundlich isotherms. Furthermore, the thermodynamic parameters of the adsorptive removal process, including ΔG°, ΔH°, and ΔS°, indicated a

  17. Degradation of 3,3'-iminobis-propanenitrile in aqueous solution by Fe(0)/GAC micro-electrolysis system.

    Science.gov (United States)

    Lai, Bo; Zhou, Yuexi; Yang, Ping; Yang, Jinghui; Wang, Juling

    2013-01-01

    The degradation of 3,3'-iminobis-propanenitrile was investigated using the Fe(0)/GAC micro-electrolysis system. Effects of influent pH value, Fe(0)/GAC ratio and granular activated carbon (GAC) adsorption on the removal efficiency of the pollutant were studied in the Fe(0)/GAC micro-electrolysis system. The degradation of 3,3'-iminobis-propanenitrile was affected by influent pH, and a decrease of the influent pH values from 8.0 to 4.0 led to the increase of degradation efficiency. Granular activated carbon was added as cathode to form macroscopic galvanic cells between Fe(0) and GAC and enhance the current efficiency of the Fe(0)/GAC micro-electrolysis system. The GAC could only adsorb the pollutant and provide buffer capacity for the Fe(0)/GAC micro-electrolysis system, and the macroscopic galvanic cells of the Fe(0)/GAC micro-electrolysis system played a leading role in degradation of 3,3'-iminobis-propanenitrile. With the analysis of the degradation products with GC-MS, possible reaction pathway for the degradation of 3,3'-iminobis-propanenitrile by the Fe(0)/GAC micro-electrolysis system was suggested. Copyright © 2012 Elsevier Ltd. All rights reserved.

  18. Selective extraction and recovery of rare earth metals from phosphor powders in waste fluorescent lamps using an ionic liquid system.

    Science.gov (United States)

    Yang, Fan; Kubota, Fukiko; Baba, Yuzo; Kamiya, Noriho; Goto, Masahiro

    2013-06-15

    The recycling of rare earth metals from phosphor powders in waste fluorescent lamps by solvent extraction using ionic liquids was studied. Acid leaching of rare earth metals from the waste phosphor powder was examined first. Yttrium (Y) and europium (Eu) dissolved readily in the acid solution; however, the leaching of other rare earth metals required substantial energy input. Ionization of target rare earth metals from the waste phosphor powders into the leach solution was critical for their successful recovery. As a high temperature was required for the complete leaching of all rare earth metals, ionic liquids, for which vapor pressure is negligible, were used as an alternative extracting phase to the conventional organic diluent. An extractant, N, N-dioctyldiglycol amic acid (DODGAA), which was recently developed, showed a high affinity for rare earth metal ions in liquid-liquid extraction although a conventional commercial phosphonic extractant did not. An effective recovery of the rare earth metals, Y, Eu, La and Ce, from the metal impurities, Fe, Al and Zn, was achieved from the acidic leach solution of phosphor powders using an ionic liquid containing DODGAA as novel extractant system. Copyright © 2013 Elsevier B.V. All rights reserved.

  19. Influence of regional hydrogeological systems at a local scale: Analyzing the coupled effects of hydrochemistry and biological activity in a Fe and CO{sub 2} rich spring

    Energy Technology Data Exchange (ETDEWEB)

    Menció, A., E-mail: anna.mencio@udg.edu [Grup de Geologia Aplicada i Ambiental (GAiA), Department of Environmental Sciences, University of Girona, Faculty of Sciences, Campus de Montilivi, 17071 Girona (Spain); Guasch, H., E-mail: helena.guasch@udg.edu [Grup de Recerca en Ecosistemes Continentals (GRECO), Institute of Aquatic Ecology, University of Girona, Faculty of Sciences, Campus de Montilivi, 17071 Girona (Spain); Soler, D.; Canelles, A.; Zamorano, M.; Brusi, D. [Grup de Geologia Aplicada i Ambiental (GAiA), Department of Environmental Sciences, University of Girona, Faculty of Sciences, Campus de Montilivi, 17071 Girona (Spain)

    2016-11-01

    A multidisciplinary approach was used in this study to determine the origin of a Fe and CO{sub 2} rich spring, an extreme freshwater system and to evaluate the coupled effects of hydrochemistry and biological activity at a local scale. An electrical resistivity tomography survey was conducted to delineate the geological context in which water emerges from a Plio-Quaternary supracrustal fault zone, and a bulk resistivity decrease was detected when CO{sub 2} rich groundwater occurred. Nine water samples, together with eight biofilm samples, and three sediment samples were taken along the spring canal for their analysis. Major ions, nutrients, and metals were analysed in water samples. Sediment analyses determined the main solid phases precipitated (mainly as CaCO{sub 3} and Fe(OH){sub 3}(a)). Biofilm analyses permitted to obtain biovolume per cell measures, total biovolume values, diatom density, chlorophyll a concentrations, and the Margalef Index values. Inverse modeling and batch reaction models were used to determine the physicochemical processes affecting the spring water, obtaining the total amount of CaCO{sub 3}/L formed; the Fe and Mn compounds, which mainly precipitated as Fe(OH){sub 3}(a) and Mn(OH){sub 2}; as well as the total CO{sub 2} released to the atmosphere. Analyzing these results together with the patterns of variation of hydrochemical and biological parameters, different interactions were observed: a) the effects of Fe inhibition in travertine formation, even though when the highest CO{sub 2} release was occurring; b) the fate and effects of chemicals limiting and/or inhibiting algal growth (mainly Fe, As and phosphate); c) the lack of coincidence between algal growth and tufa limestone precipitation; d) the relationship between some divalent metals (Mn and Co) and biotic activity. - Highlights: • Electrical resistivity tomography detected CO{sub 2} rich groundwater. • High Fe concentrations inhibits both algal growth and CaCO{sub 3

  20. Development of a wear-resistant flux cored wire of Fe-C-Si-Mn-Cr-Ni-Mo-V system for deposit welding of mining equipment parts

    Science.gov (United States)

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

    2017-09-01

    The effect of introduction of cobalt in the charge of the flux cored wire of Fe-C-Si-Mn-Cr-Ni-Mo-V system operating under abrasive and abrasive-shock loads is studied. In the laboratory conditions samples of flux cored wires were made, deposition was performed, the effect of cobalt on the hardness and the degree of wear was evaluated, metallographic studies were carried out. The influence of cobalt introduced into the charge of the flux cored wire of Fe-C-Si-Mn-Cr-Ni-Mo-V system on the structure, nature of nonmetallic inclusions, hardness and wear resistance of the weld metal was studied. In the laboratory conditions samples flux cored wire were made using appropriate powdered materials. As a carbon-fluorine-containing material dust from gas cleaning units of aluminum production was used. In the course of the study the chemical composition of the weld metal was determined, metallographic analysis was performed, mechanical properties were determined. As a result of the metallographic analysis the size of the former austenite grain, martensite dispersion in the structure of the weld metal, the level of contamination with its nonmetallic inclusions were established.

  1. FE-I4 pixel chip characterization with USBpix3 test system

    Energy Technology Data Exchange (ETDEWEB)

    Filimonov, Viacheslav; Gonella, Laura; Hemperek, Tomasz; Huegging, Fabian; Janssen, Jens; Krueger, Hans; Pohl, David-Leon; Wermes, Norbert [University of Bonn, Bonn (Germany)

    2015-07-01

    The USBpix readout system is a small and light weighting test system for the ATLAS pixel readout chips. It is widely used to operate and characterize FE-I4 pixel modules in lab and test beam environments. For multi-chip modules the resources on the Multi-IO board, that is the central control unit of the readout system, are coming to their limits, which makes the simultaneous readout of more than one chip at a time challenging. Therefore an upgrade of the current USBpix system has been developed. The upgraded system is called USBpix3 - the main focus of the talk. Characterization of single chip FE-I4 modules was performed with USBpix3 prototype (digital, analog, threshold and source scans; tuning). PyBAR (Bonn ATLAS Readout in Python scripting language) was used as readout software. PyBAR consists of FEI4 DAQ and Data Analysis Libraries in Python. The presentation describes the USBpix3 system, results of FE-I4 modules characterization and preparation for the multi-chip module and multi-module readout with USBpix3.

  2. EVLA OBSERVATIONS CONSTRAIN THE ENVIRONMENT AND PROGENITOR SYSTEM OF Type Ia SUPERNOVA 2011fe

    International Nuclear Information System (INIS)

    Chomiuk, Laura; Soderberg, Alicia M.; Moe, Maxwell; Margutti, Raffaella; Fong, Wen-fai; Dittmann, Jason A.; Chevalier, Roger A.; Rupen, Michael P.; Badenes, Carles; Fransson, Claes

    2012-01-01

    We report unique Expanded Very Large Array observations of SN 2011fe representing the most sensitive radio study of a Type Ia supernova to date. Our data place direct constraints on the density of the surrounding medium at radii ∼10 15 -10 16 cm, implying an upper limit on the mass loss rate from the progenitor system of M-dot -10 M ☉ yr -1 (assuming a wind speed of 100 km s –1 ) or expansion into a uniform medium with density n CSM ∼ –3 . Drawing from the observed properties of non-conservative mass transfer among accreting white dwarfs, we use these limits on the density of the immediate environs to exclude a phase space of possible progenitor systems for SN 2011fe. We rule out a symbiotic progenitor system and also a system characterized by high accretion rate onto the white dwarf that is expected to give rise to optically thick accretion winds. Assuming that a small fraction, 1%, of the mass accreted is lost from the progenitor system, we also eliminate much of the potential progenitor parameter space for white dwarfs hosting recurrent novae or undergoing stable nuclear burning. Therefore, we rule out much of the parameter space associated with popular single degenerate progenitor models for SN 2011fe, leaving a limited phase space largely inhabited by some double degenerate systems, as well as exotic single degenerates with a sufficient time delay between mass accretion and SN explosion.

  3. Evaluation of the heavy metals Cr, Mn, Fe, Cu, Zn and Pb in water penny wort (Hydrocotyle ranunculoides) from the upper course of the Lerma River, Mexico; Evaluacion de los metales pesados Cr, Mn, Fe, Cu, Zn y Pb en sombrerillo de agua (Hydrocotyle ranunculoides) del curso alto del Rio Lerma, Mexico

    Energy Technology Data Exchange (ETDEWEB)

    Zarazua, G.; Avila P, P.; Tejeda, S. [ININ, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico); Valdivia B, M.; Macedo M, G. [Instituto Tecnologico de Toluca, Av. Tecnologico s/n, Ex-Rancho La Virgen, 52140 Metepec, Estado de Mexico (Mexico); Zepeda G, C., E-mail: graciela.zarazua@inin.gob.mx [Universidad Autonoma del Estado de Mexico, Cerro de Coatepec s/n, Ciudad Universitaria, 50100 Toluca, Estado de Mexico (Mexico)

    2013-07-01

    The Lerma river is one of the most polluted water bodies in Mexico, it presents low biodiversity and lets grow up aquatic plants resistant to the pollution. The aim of this work was to evaluate the concentration and bioaccumulation factors of Cr, Mn, Fe, Cu, Zn and Pb in aerial and submerged structures of water penny wort (Hydrocotyle ranunculoides) from the upper course of the Lerma river. Inductively coupled plasma-optical emission spectrometry was used to determine the concentration of heavy metals in water and H. ranunculoides. Results show that the bioaccumulation factors of Fe and Zn were higher than those of Cu, Mn, Cr and Pb; with the exception of Zn, bioaccumulation factors were higher in the submerged structures of the plant, which shows low mobility of analyzed metals. As a result of this study H. ranunculoides can be considered as good indicator of metal pollution in water bodies. (Author)

  4. An iron complex with an unsupported Fe-Fe bond.

    Science.gov (United States)

    Murillo, Carlos A

    2009-01-01

    Full metal bonding: The reduction of a six-coordinate, mononuclear Werner-type iron(II) complex (see scheme) resulted in the isolation of a compound with an extraordinarily rare, unsupported Fe-Fe bond having an experimental Fe-Fe distance of 2.6869(6) A and a calculated bond order of 0.5.

  5. Surface Complexation Modelling in Metal-Mineral-Bacteria Systems

    Science.gov (United States)

    Johnson, K. J.; Fein, J. B.

    2002-12-01

    The reactive surfaces of bacteria and minerals can determine the fate, transport, and bioavailability of aqueous heavy metal cations. Geochemical models are instrumental in accurately accounting for the partitioning of the metals between mineral surfaces and bacteria cell walls. Previous research has shown that surface complexation modelling (SCM) is accurate in two-component systems (metal:mineral and metal:bacteria); however, the ability of SCMs to account for metal distribution in mixed metal-mineral-bacteria systems has not been tested. In this study, we measure aqueous Cd distributions in water-bacteria-mineral systems, and compare these observations with predicted distributions based on a surface complexation modelling approach. We measured Cd adsorption in 2- and 3-component batch adsorption experiments. In the 2-component experiments, we measured the extent of adsorption of 10 ppm aqueous Cd onto either a bacterial or hydrous ferric oxide sorbent. The metal:bacteria experiments contained 1 g/L (wet wt.) of B. subtilis, and were conducted as a function of pH; the metal:mineral experiments were conducted as a function of both pH and HFO content. Two types of 3-component Cd adsorption experiments were also conducted in which both mineral powder and bacteria were present as sorbents: 1) one in which the HFO was physically but not chemically isolated from the system using sealed dialysis tubing, and 2) others where the HFO, Cd and B. subtilis were all in physical contact. The dialysis tubing approach enabled the direct determination of the concentration of Cd on each sorbing surface, after separation and acidification of each sorbent. The experiments indicate that both bacteria and mineral surfaces can dominate adsorption in the system, depending on pH and bacteria:mineral ratio. The stability constants, determined using the data from the 2-component systems, along with those for other surface and aqueous species in the systems, were used with FITEQL to

  6. Polymer filtration systems for dilute metal ion recovery

    Energy Technology Data Exchange (ETDEWEB)

    Smith, B.F.; Robison, T.W.; Jarvinen, G.D.

    1998-12-01

    Scientists at Los Alamos National Laboratory have developed a metal recovery system that meets the global treatment demands for all kinds of industrial and metal-processing streams. The Polymer Filtration (PF) System--a process that is easily operated and robust--offers metal-finishing businesses a convenient and inexpensive way to recover and recycle metal ions in-house, thus reducing materials costs, waste removal costs, and industrial liability. As a valuable economic and environmental asset, the PF System has been named a winner of a 1995 R and D 100 Award. These awards are presented annually by R and D Magazine to the one hundred most significant technical innovations of the year. The PF System is based on the use of water-soluble metal-binding polymers and on advanced ultrafiltration membranes. Customers for this technology will receive new soluble polymers, especially formulated for their waste stream, and the complete PF processing unit: a reaction reservoir, pumps, plumbing, controls, and the advanced ultrafiltration membranes, all in a skid mounted frame. Metal-bearing waste water is treated in the reaction reservoir, where the polymer binds with the metal ions under balanced acid/base conditions. The reservoir fluid is then pumped through the ultrafiltration system--a cartridge packed with ultrafiltration membranes shaped in hollow fibers. As the fluid travels inside the fiber, water and other small molecules--simple salts such as calcium and sodium, for example--pass through the porous membrane walls of the fibers and are discharged through the outlet as permeate. The polymer-bound metal, which is too large to pass through the pores, is both purified and concentrated inside the hollow fibers and is returned to the fluid reservoir for further waste water treatment.

  7. Metal Allergy and Systemic Contact Dermatitis: An Overview

    Directory of Open Access Journals (Sweden)

    Yoko Yoshihisa

    2012-01-01

    Full Text Available Contact dermatitis is produced by external skin exposure to an allergen, but sometimes a systemically administered allergen may reach the skin and remain concentrated there with the aid of the circulatory system, leading to the production of systemic contact dermatitis (SCD. Metals such as nickel, cobalt, chromium, and zinc are ubiquitous in our environment. Metal allergy may result in allergic contact dermatitis and also SCD. Systemic reactions, such as hand dermatitis or generalized eczematous reactions, can occur due to dietary nickel or cobalt ingestion. Zinc-containing dental fillings can induce oral lichen planus, palmoplantar pustulosis, and maculopapular rash. A diagnosis of sensitivity to metal is established by epicutaneous patch testing and oral metal challenge with metals such as nickel, cobalt, chromium, and zinc. In vitro tests, such as the lymphocyte stimulating test (LST, have some advantages over patch testing to diagnose allergic contact dermatitis. Additionally, the determination of the production of several cytokines by primary peripheral blood mononuclear cell cultures is a potentially promising in vitro method for the discrimination of metal allergies, including SCD, as compared with the LST.

  8. Prospective Comparison of a Metal-Free Ceramic Total Knee Arthroplasty with an Identical Metal System.

    Science.gov (United States)

    Trieb, Klemens; Ullmann, David; Metzinger, Katharina; Kramar, Reinhard; Mauerer, Andreas; Hofstätter, Stefan; Fiala, Rainer

    2018-02-01

    The aim of this open-label, prospective, short-term study was to carry out an initial comparison of a completely metal-free ceramic with a geometrically identical metallic arthroplasty over a 1-year follow-up period. This study investigates a completely metal-free system using a composite matrix material containing aluminum oxide (Al 2 O 3 , BPK-S Integration, Peter Brehm GmbH, Weisendorf, Germany) or zirconium oxide (ZrO 2 , BPK-S Integration Ceramic, Biolox Delta-CeramTec GmbH, Plochingen, Germany). Eighty patients (40 in each group) received either a completely metal-free ceramic system (matrix of aluminum and zirconium oxide) or an anatomically identical metallic knee system made of a cobalt-chromium alloy. Clinical assessment was performed preoperatively, and during follow-up at 3 and 12 months, using the Knee Society Score, Oxford Knee Score, and EQ-5D-VAS. For radiological evaluation, standard preoperative and postoperative standardized radiographs were taken at the given follow-up visits. The postoperative clinical scores improved significantly at the 3- and 12-month follow-ups, but did not differ statistically between the two groups. The radiologically evaluated mean postoperative mechanical and anatomical axes showed proper alignment within both groups at all times. No revision surgery had to be performed, and no complications or loosening were recorded whatsoever. To our knowledge, this is the first study comparing a total ceramic metal-free knee system with a geometrically identical metallic TKA (total knee arthroplasty). Longer follow-ups will be required to demonstrate the overall efficiency of this TKR and perhaps to expand its medical indication. Georg Thieme Verlag KG Stuttgart · New York.

  9. Photoelectrochemical energy conversion obtained with ultrathin organo-metallic-chemical-vapor-deposition layer of FeS2 (pyrite) on TiO2

    International Nuclear Information System (INIS)

    Ennaoui, A.; Fiechter, S.; Tributsch, H.; Giersig, M.; Vogel, R.; Weller, H.

    1992-01-01

    Ultrathin (10 to 20 nm thick), polycrystalline films of FeS 2 (pyrite) were grown on TiO 2 (anatase) by chemical vapor deposition. The FeS 2 films were characterized using optical absorption and high-resolution electron microscopy. Photoelectrochemical solar cells, using TiO 2 (anatase) coated with FeS 2 ultrathin films, generated high open-circuit photo-voltages, of up to 600 mV, compared with a single crystal of pyrite electrode (200 mV). The photoelectrochemical behavior shows a strong dependence of photovoltage and photocurrent on the pH of the solution. This paper reports that it is explained by electron injection from the conduction band of FeS 2 to the conduction band of TiO 2 . Regeneration of holes is taking place by electron transfer from the redox system in the electrolyte

  10. Photoelectrochemical energy conversion obtained with ultrathin organo-metallic-chemical-vapor-deposition layer of FeS[sub 2] (pyrite) on TiO[sub 2

    Energy Technology Data Exchange (ETDEWEB)

    Ennaoui, A.; Fiechter, S.; Tributsch, H. (Abt. Solare Energetik, Hahn-Meitner-Inst., D-1000 Berlin 39 (Germany)); Giersig, M.; Vogel, R.; Weller, H. (Abt. Photochemie, Hahn-Meitner-Inst., D-1000 Berlin 39 (Germany))

    1992-09-01

    Ultrathin (10 to 20 nm thick), polycrystalline films of FeS[sub 2] (pyrite) were grown on TiO[sub 2] (anatase) by chemical vapor deposition. The FeS[sub 2] films were characterized using optical absorption and high-resolution electron microscopy. Photoelectrochemical solar cells, using TiO[sub 2] (anatase) coated with FeS[sub 2] ultrathin films, generated high open-circuit photo-voltages, of up to 600 mV, compared with a single crystal of pyrite electrode (200 mV). The photoelectrochemical behavior shows a strong dependence of photovoltage and photocurrent on the pH of the solution. This paper reports that it is explained by electron injection from the conduction band of FeS[sub 2] to the conduction band of TiO[sub 2]. Regeneration of holes is taking place by electron transfer from the redox system in the electrolyte.

  11. An assessment of heavy metal contamination in soils of fresh water aquifer system and evaluation of eco-toxicity by lithogenic implications.

    Science.gov (United States)

    Harichandan, R; Routroy, S; Mohanty, J K; Panda, C R

    2013-04-01

    The chemistry of heavy metals in sediments with respect to bio-availability and chemical reactivity is regulated by pH, texture, and organic matter contents of the sediments and specific binding form and coupled reactivity of the metals within. To focus on the metal distribution (Fe, Mn, Pb, Cd, Zn, Co, Cu, and Cr) and behavior in a fresh water aquifer system along with the ecological toxicity parameters, a four-step sequential extraction method was applied on 18 Eastern Ghats' type sediments from fluorosis-hit Nayagarh district, India. Geo-accumulation index of metals in the sediments indicates that they are practically uncontaminated and/or less contaminated with and Fe, Mn, and Cu; contaminated to moderately contaminated with Pb, Zn, and Cr; and strongly contaminated with Cd. Rather, more than 80 % recovered Cd metal concentration in sediments constitute the labile fractions. Temporal clustering of metal fractions indicates transition metal fraction distribution claiming the sediment pH regulation. Similarly, base metal distribution accounts for organic carbon and soil conductivity due to their greater availability in exchangeable and sulfide fractions. Correlation analysis and factor analysis scores demonstrate lack of inter-relationship between transition group and base metal fractions. High fluoride concentration in ground water is associated with high sodium-bicarbonate-iron affinity with elevated pH values (i.e., >7.0) and high positive factor score with the total iron concentration in ground water.

  12. A Bio-Electro-Fenton System Employing the Composite FePc/CNT/SS316 Cathode

    Directory of Open Access Journals (Sweden)

    Yi-Ta Wang

    2017-02-01

    Full Text Available Bio-electro-Fenton microbial fuel cells generate energy through the decomposition of organic matter by microorganisms. The generated electricity drives a Fenton reaction in a cathode chamber, which can be used for the decolorization of dye wastewater. Most of the previous works added expensive platinum catalyst to improve the electrical property of the system. In this research, aligned carbon nanotubes (CNTs were generated on the surface of SS316 stainless steel by chemical vapor deposition, and an iron phthalocyanine (FePc catalyst was added to fabricate a compound (FePc/CNT/SS316 that was applied to the cathode electrode of the fuel cell system. This was expected to improve the overall electricity generation efficiency and extent of decolorization of the system. The results showed that the maximum current density of the system with the modified electrode was 3206.30 mA/m2, and the maximum power was 726.55 mW/m2, which were increased by 937 and 2594 times, respectively, compared to the current and power densities of a system where only the SS316 stainless steel electrode was used. In addition, the decolorization of RB5 dye reached 84.6% within 12 h. Measurements of the electrical properties of bio-electro-Fenton microbial fuel cells and dye decolorization experiments with the FePc/CNT/SS316 electrode showed good results.

  13. Evaluation of heavy metals (Cr, Fe, Ni, Cu, Zn, Cd, Pb and Hg) in water, sediments and water lily (Eichornia crassipes) from Jose Antonio Alzate dam

    International Nuclear Information System (INIS)

    Avila P, P.

    1995-01-01

    Water, sediments and water lily (Eichornia crassipes) from the Jose Antonio Alzate Dam were analyzed in order to determine concentrations of chromium, iron, nickel, copper, zinc, cadmium, lead and mercury. Mercury, lead, chromium and iron were found in concentrations above permissible limits in water, and in high concentrations in sediments. Cadmium, nickel, copper and zinc never were found in concentrations above permissible limits in water. The highest concentrations of heavy metals in water lily were found in the root. Accumulation factors decreased in the following order: Zn> Cr> Fe> Ni> Cu> Pb> Hg and Cd. Statistical differences (α < 0.5) between the collection samples dates was observed. High correlations between metals concentrations in superficial water, sediment and water hyacinth were also observed. These correlations could indicate that the heavy metals studied here, are originated from a natural source such as sediments or from an industrial source. (Author)

  14. Proceedings of the joint contractors meeting: FE/EE Advanced Turbine Systems conference FE fuel cells and coal-fired heat engines conference

    Energy Technology Data Exchange (ETDEWEB)

    Geiling, D.W. [ed.

    1993-08-01

    The joint contractors meeting: FE/EE Advanced Turbine Systems conference FEE fuel cells and coal-fired heat engines conference; was sponsored by the US Department of Energy Office of Fossil Energy and held at the Morgantown Energy Technology Center, P.O. Box 880, Morgantown, West Virginia 26507-0880, August 3--5, 1993. Individual papers have been entered separately.

  15. Study of the ZrO2-FeO-Fe2O3 system by thermogravimetry in partial pressure of oxygen and temperatures up to 15000C

    International Nuclear Information System (INIS)

    Goldschmidt, R.H.; Kiminami, A.

    1987-01-01

    The dissociation of iron oxide in the ZrO 2 -FeO-Fe 2 O 3 system was investigated in function of the temperature and the constant partial pressure of oxygen by thermal gravimetric analysis. The equilibrium diagram was constructed where the equilibrium relation between the solid phase of zirconium oxide, hematite and magnetite in 1437 0 C and PO 2 = 0.21 atm/m, as well as the equilibrium relation between the solid phase of zirconium oxide and hematite in lower temperatures than 1437 0 C were determined [pt

  16. Role of neutron activation analysis in the study of heavy metal pollution of a lake-river system

    International Nuclear Information System (INIS)

    Filby, R.H.; Shah, K.R.; Funk, W.H.

    1974-01-01

    Details of a study of combined organic and metallic pollution of the Coeur d'Alene Lake-River and Spokane River system and the role played by nuclear techniques in the investigation are presented. The Coeur d'Alene River drains through the N. Idaho Pb--Zn mining region of Kellogg and the mining industry is the major source of metallic pollution of the lake and river system. The first part of the study has involved the determination of Pb, Zn, Ag, Cd, As, Cu, Sb, Co, Cr, Cs, Rb, Sc, Ba, Eu, La, Tb, Y, Zr, Fe, Mn, Mo, by INAA in waters, sediments and organisms throughout the region. Extremely high values for Pb, Zn, Sb, Fe and other metals were found in the Coeur d'Alene River delta sediments and in the lake sediments. Results from the study of metals in an aquatic ecosystem show the value of combining nuclear techniques with other methods of trace analysis in practical pollution problems

  17. System and method for producing metallic iron

    Science.gov (United States)

    Bleifuss, Rodney L; Englund, David J; Iwasaki, Iwao; Fosnacht, Donald R; Brandon, Mark M; True, Bradford G

    2013-09-17

    A hearth furnace for producing metallic iron material has a furnace housing having a drying/preheat zone, a conversion zone, a fusion zone, and optionally a cooling zone, the conversion zone is between the drying/preheat zone and the fusion zone. A moving hearth is positioned within the furnace housing. A hood or separation barrier within at least a portion of the conversion zone, fusion zone or both separates the fusion zone into an upper region and a lower region with the lower region adjacent the hearth and the upper region adjacent the lower region and spaced from the hearth. An injector introduces a gaseous reductant into the lower region adjacent the hearth. A combustion region may be formed above the hood or separation barrier.

  18. Structure and magnetic properties of the 3d transition-metal mono-borides TM–B (TM=Mn, Fe, Co) under pressures

    International Nuclear Information System (INIS)

    Bourourou, Y.; Beldi, L.; Bentria, B.; Gueddouh, A.; Bouhafs, B.

    2014-01-01

    In this paper, spin-polarization and pressure effects on the structural and electronic properties of the 3d transition-metal mono-borides TM–B (TM=Mn, Fe, Co) have been studied by using both local spin-density approximation (LSDA) and generalized gradient approximation (GGA) within the framework of density-functional theory (DFT). At equilibrium, spin-polarization calculations show that MnB and FeB compounds carry magnetic moment. The non-spin-polarization results show that the non-magnetic state is unstable for MnB and FeB compounds, but a stable non-magnetic phase for CoB compound, which is discussed in the framework of the well-known Stoner criterion. The calculated lattice parameters, bulk moduli, their first-pressure derivatives and magnetic moments agree well with experimental and other theoretical results. Significant differences in volume and in bulk modulus were found between the magnetic and non-magnetic case reached 4%, 22%, respectively. The effect of pressure on the crystal structure reflects in a compression of the unit cell volume with a decreasing in the magnetic moment. The density of states of MnB and FeB ferromagnetic compounds are significantly modified under high pressures. The exchange energy decreases with increasing pressure, at approximately V/V 0 =0.6, the exchange energy becomes absent in ferromagnetic compounds causes mirror in upper and lowers half panels. Finally, we notice that spin-polarization and pressure play a crucially important role in determining the electronic and structural properties of 3d transition-metal mono-borides. - Highlights: • Spin polarization and pressure effects on TM–B (TM=Mn, Fe, Co) have been investigated. • The non-spin-polarization results show that the non-magnetic state is stable for CoB. • The magnetic states of MnB and FeB are found more stable than their nonmagnetic states. • We report significant differences between the magnetic and non-magnetic cases. • The density of states of MnB and

  19. Synthesis and order-disorder transition in a novel metal formate framework of [(CH₃)₂NH₂]Na(0.5)Fe(0.5)(HCOO)₃].

    Science.gov (United States)

    Mączka, Mirosław; Pietraszko, Adam; Macalik, Lucyna; Sieradzki, Adam; Trzmiel, Justyna; Pikul, Adam

    2014-12-07

    We report the synthesis, crystal structure, thermal, dielectric, Raman, infrared, and magnetic properties of [(CH3)2NH2][Na(0.5)Fe(0.5)(HCOO)3] (DMNaFe), the first metal formate framework templated by organic cations, presenting an ABO3 perovskite architecture with NaO6 octahedra as building blocks of the framework. On the basis of Raman and IR data, assignment of the observed modes to respective vibrations of atoms is proposed. We have found that DMNaFe undergoes a structural phase transition at 167 K on cooling. According to the X-ray diffraction, the compound shows R3[combining macron] symmetry at 293 K and triclinic P1[combining macron] symmetry at 110 K. The DMA(+) cations are dynamically disordered in the high-temperature phase and the phase transition is associated with ordering of the DMA(+) cations and distortion of the metal formate framework. The dielectric studies reveal pronounced dielectric dispersion that can be attributed to slow dynamics of the DMA(+) cations. Based on the low-temperature magnetic studies, this compound is a weak ferromagnet with a critical temperature 8.5 K.

  20. Alloying Behavior and Properties of Al-Based Composites Reinforced with Al85Fe15 Metallic Glass Particles Fabricated by Mechanical Alloying and Hot Pressing Consolidation

    Science.gov (United States)

    Zhang, Lanxiang; Yang, LiKun; Leng, Jinfeng; Wang, Tongyang; Wang, Yan

    2017-04-01

    In this study, Al85Fe15 metallic glass particles with high onset crystallization temperature (1209 K) were synthesized by a mechanical alloying method. High-quality 6061Al-based composites reinforced with Al85Fe15 metallic glass particles were fabricated by a vacuum hot-pressing sintering technique. The glass particles with flake-like shape are distributed uniformly in the Al matrix. The bulk composites possess high relative density, excellent hardness and strength. The microhardness values of the Al-based bulk composites with the additions of 20 vol.% and 30 vol.% Al85Fe15 particles are 204 MPa and 248 MPa, respectively, which are much higher than that of 6061Al (61 MPa). The compressive yield strength of the 30 vol.% glass-reinforced composite is 478 MPa, which is enhanced by 273% compared with 6061Al. The amorphous characteristic and homogeneous dispersion of glass particles account for the excellent mechanical properties of the Al-based composites. In addition, the corrosion behavior of Al-based composites in a seawater solution has been investigated by electrochemical polarization measurements. Compared to 6061Al, the 30 vol.% glass-reinforced composite shows the lower corrosion/passive current density and larger passive region, indicating the greatly enhanced corrosion resistance.

  1. Magnetization of ternary alloys based on Fe0.65Ni0.35 invar with 3d transition metal additions: An ab initio study

    Science.gov (United States)

    Onoue, Masatoshi; Trimarchi, Giancarlo; Freeman, Arthur J.; Popescu, Voicu; Matsen, Marc R.

    2015-01-01

    Smart susceptors are being developed for use as tooling surfaces in molding machines that use apply electro-magnetic induction heating to mold and form plastics or metal powders into structural parts, e.g., on aerospace and automotive manufacturing lines. The optimal magnetic materials for the induction heating process should have large magnetization, high magnetic permeability, but also small thermal expansion coefficient. The Fe0.65Ni0.35 invar alloy with its negligible thermal expansion coefficient is thus a natural choice for this application. Here, we use density functional theory as implemented through the Korringa-Kohn-Rostoker method within the coherent-potential approximation, to design new alloys with the large magnetization desired for smart susceptor applications. We consider the Fe0.65-xNi0.35-yMx+y alloys derived from Fe0.65Ni0.35 invar adding a third element M = Sc, Ti, V, Cr, Mn, or Co with concentration (x + y) reaching up to 5 at. %. We find that the total magnetization depends linearly on the concentration of M. Specifically, the early 3d transition metals from Sc to Cr decrease the magnetization with respect to that of the invar alloy whereas Mn and Co increase it.

  2. Experimental study and thermodynamic modeling of the phase relation in the Fe-S-Si system with implications for the distribution of S and Si in a partially solidified core

    Science.gov (United States)

    Tao, R.; Fei, Y.

    2017-12-01

    Planetary cooling leads to solidification of any initially molten metallic core. Some terrestrial cores (e.g. Mercury) are formed and differentiated under relatively reduced conditions, and they are thought to be composed of Fe-S-Si. However, there are limited understanding of the phase relations in the Fe-S-Si system at high pressure and temperature. In this study, we conducted high-pressure experiments to investigate the phase relations in the Fe-S-Si system up to 25 GPa. Experimental results show that the liquidus and solidus in this study are slightly lower than those in the Fe-S binary system for the same S concentration in liquid at same pressure. The Fe3S, which is supposed to be the stable sub-solidus S-bearing phase in the Fe-S binary system above 17 GPa, is not observed in the Fe-S-Si system at 21 GPa. Almost all S prefers to partition into liquid, while the distribution of Si between solid and liquid depends on experimental P and T conditions. We obtained the partition coefficient log(KDSi) by fitting the experimental data as a function of P, T and S concentration in liquid. At a constant pressure, the log(KDSi) linearly decreases with 1/T(K). With increase of pressure, the slopes of linear correlation between log(KDSi) and 1/T(K) decreases, indicating that more Si partitions into solid at higher pressure. In order to interpolate and extrapolate the phase relations over a wide pressure and temperature range, we established a comprehensive thermodynamic model in the Fe-S-Si system. The results will be used to constrain the distribution of S and Si between solid inner core and liquid outer core for a range of planet sizes. A Si-rich solid inner core and a S-rich liquid outer core are suggested for an iron-rich core.

  3. Magnetic ground state of Ti1-xScxFe2 system

    International Nuclear Information System (INIS)

    Saoudi, M.; Deportes, J.; Ouladdiaf, B.

    2001-01-01

    The magnetic ground states of the Laves phases Ti 1-x Sc x Fe 2 system have been investigated by means of powder neutron diffraction and magnetisation techniques. For x=0.23, a transition is observed from a collinear ferromagnet along the c-axis to a canted one at T f =200 K. For x=0.27, 0.3, 0.33, an additional first-order transition is observed at T t1 ∼120 K accompanied by a large magnetovolume anomaly associated to a jump of the magnetic moment of the Fe atoms at the 2a site. The magnetic moment instability in a frustrated lattice should be considered to interpret this transition, although most of the other magnetic states can be discussed within Moriya's theory for itinerant electron systems with competing ferromagnetic and antiferromagnetic spin fluctuations

  4. Magnetic porous Fe3O4/carbon octahedra derived from iron-based metal-organic framework as heterogeneous Fenton-like catalyst

    Science.gov (United States)

    Li, Wenhui; Wu, Xiaofeng; Li, Shuangde; Tang, Wenxiang; Chen, Yunfa

    2018-04-01

    The synthesis of effective and recyclable Fenton-like catalyst is still a key factor for advanced oxidation processes. Herein, magnetic porous Fe3O4/carbon octahedra were constructed by a two-step controlled calcination of iron-based metal organic framework. The porous octahedra were assembled by interpenetrated Fe3O4 nanoparticles coated with graphitic carbon layer, offering abundant mesoporous channels for the solid-liquid contact. Moreover, the oxygen-containing functional groups on the surface of graphitic carbon endow the catalysts with hydrophilic nature and well-dispersion into water. The porous Fe3O4/carbon octahedra show efficiently heterogeneous Fenton-like reactions for decomposing the organic dye methylene blue (MB) with the help of H2O2, and nearly 100% removal efficiency within 60 min. Furthermore, the magnetic catalyst retains the activity after ten cycles and can be easily separated by external magnetic field, indicating the long-term catalytic durability and recyclability. The good Fenton-like catalytic performance of the as-synthesized Fe3O4/carbon octahedra is ascribed to the unique mesoporous structure derived from MOF-framework, as well as the sacrificial role and stabilizing effect of graphitic carbon layer. This work provides a facile strategy for the controllable synthesis of integrated porous octahedral structure with graphitic carbon layer, and thereby the catalyst holds significant potential for wastewater treatment.

  5. Selective extraction and recovery of rare earth metals from phosphor powders in waste fluorescent lamps using an ionic liquid system

    International Nuclear Information System (INIS)

    Yang, Fan; Kubota, Fukiko; Baba, Yuzo; Kamiya, Noriho; Goto, Masahiro

    2013-01-01

    Highlights: • Recycling of rare earth metals from fluorescent lamps was conducted by ionic liquid-mediated extraction. • Acid leaching from a waste phosphor powder was carried out using sulfuric and nitric acids. • An ionic liquid was used as extracting solvent for the rare earth metals. • Selective extraction of rare earth metals from leach solutions was attained. •The extracting ionic liquid phase was recyclable in the recovery process. -- Abstract: The recycling of rare earth metals from phosphor powders in waste fluorescent lamps by solvent extraction using ionic liquids was studied. Acid leaching of rare earth metals from the waste phosphor powder was examined first. Yttrium (Y) and europium (Eu) dissolved readily in the acid solution; however, the leaching of other rare earth metals required substantial energy input. Ionization of target rare earth metals from the waste phosphor powders into the leach solution was critical for their successful recovery. As a high temperature was required for the complete leaching of all rare earth metals, ionic liquids, for which vapor pressure is negligible, were used as an alternative extracting phase to the conventional organic diluent. An extractant, N, N-dioctyldiglycol amic acid (DODGAA), which was recently developed, showed a high affinity for rare earth metal ions in liquid–liquid extraction although a conventional commercial phosphonic extractant did not. An effective recovery of the rare earth metals, Y, Eu, La and Ce, from the metal impurities, Fe, Al and Zn, was achieved from the acidic leach solution of phosphor powders using an ionic liquid containing DODGAA as novel extractant system

  6. Activity of Aniline Methylation over Fe-Cu-Cr Ternary Spinel Systems

    Directory of Open Access Journals (Sweden)

    Reni George

    2014-03-01

    Full Text Available A series of spinels having thegeneral formula CuCr2-xFexO4 with x=0.25,0.75, 1.25, 1.75 were prepared by co-precipitation method. The catalysts werecharacterized by various physico-chemical methods like XRD, BET, UV-DRS, SEM,EDX, TPD etc. The reaction of aniline with methanol was studied in a fixed-bedreactor system as a potential source for the production of various methylanilines. It was observed that systems possessing low ‘x’ values are highlyselective and active for N-monoalkylation of aniline leading toN-methylaniline. Reaction parameters were properly varied to optimize thereaction conditions for obtaining N-methylaniline selectively and in betteryield. Among the systems CuCr1.75Fe0.25O4 isremarkable due to its very high activity and excellent stability. Under theoptimized conditions N-methylaniline selectivity exceeded 91%. CuCr1.25Fe0.75O4gives better conversion than CuCr1.75Fe0.25O4in CuCr2-xFexO4 series. The Lewis acid sitesof the catalysts are mainly responsible for the good catalytic performance. © 2014 BCREC UNDIP. All rights reservedSubmitted: 18th July 2013; Revised: 5th November 2013; Accepted: 1st December 2013[How to Cite: George, R., George, K., Sugunan, S. (2014. Activity of Aniline Methylation over Fe-Cu-Cr Ternary Spinel Systems. Bulletin of Chemical Reaction Engineering & Catalysis, 9 (1: 39-44. (doi:10.9767/bcrec.9.1.5169.39-44][Permalink/DOI: http://dx.doi.org/10.9767/bcrec.9.1.5169.39-44] 

  7. Thermal performance of Fe-Cr-Nb-B systems in magnetic hyperthermia

    Science.gov (United States)

    Astefanoaei, Iordana; Chiriac, Horia; Stancu, Alexandru

    2017-03-01

    In magnetic hyperthermia, the temperature control within the malignant tissues is an important step to increase the efficiency of the therapy. A temperature analysis is a good method to improve the heating process of the magnetic particles injected within tissues. This paper analyzes the thermal effects induced within malignant tissues by the magnetic systems like: magnetite and Fe-Cr-Nb-B when an external time-dependent magnetic field is applied. The heat generation by Néel and Brown relaxations was modeled using the thermal and magnetic properties of the Fe-Cr-Nb-B particles experimentally determined. A lognormal particle size distribution was considered for these magnetic systems with dimensions from 5 nm to 30 nm. After their injection at the center of the tumor, according to the solution of the transient convection-diffusion equation in a porous medium, the mass concentration of the particles within ferrofluid has a spatial and temporal distribution. The ferrofluid injection process was modeled using the Brinkman equations. The ferrofluid injection rate during the injection process influences significantly the spatial distribution of the particle concentration and temperature field within tumor. Higher values of the ferrofluid flow rate determine a strong convection of the particles to the tumor center. As a consequence, the temperature gradients within tumor are smaller. The performance in Magnetic Hyperthermia of Fe-Cr-Nb-B magnetic systems is discussed.

  8. Metal hydride-based thermal energy storage systems

    Science.gov (United States)

    Vajo, John J.; Fang, Zhigang

    2017-10-03

    The invention provides a thermal energy storage system comprising a metal-containing first material with a thermal energy storage density of about 1300 kJ/kg to about 2200 kJ/kg based on hydrogenation; a metal-containing second material with a thermal energy storage density of about 200 kJ/kg to about 1000 kJ/kg based on hydrogenation; and a hydrogen conduit for reversibly transporting hydrogen between the first material and the second material. At a temperature of 20.degree. C. and in 1 hour, at least 90% of the metal is converted to the hydride. At a temperature of 0.degree. C. and in 1 hour, at least 90% of the metal hydride is converted to the metal and hydrogen. The disclosed metal hydride materials have a combination of thermodynamic energy storage densities and kinetic power capabilities that previously have not been demonstrated. This performance enables practical use of thermal energy storage systems for electric vehicle heating and cooling.

  9. Enhancement in the interfacial perpendicular magnetic anisotropy and the voltage-controlled magnetic anisotropy by heavy metal doping at the Fe/MgO interface

    Directory of Open Access Journals (Sweden)

    Takayuki Nozaki

    2018-02-01

    Full Text Available We investigated the influence of heavy metal doping at the Fe/MgO interface on the interfacial perpendicular magnetic anisotropy (PMA and the voltage-controlled magnetic anisotropy (VCMA in magnetic tunnel junctions prepared by sputtering-based deposition. The interfacial PMA was increased by tungsten doping and a maximum intrinsic interfacial PMA energy, Ki,0 of 2.0 mJ/m2 was obtained. Ir doping led to a large increase in the VCMA coefficient by a factor of 4.7 compared with that for the standard Fe/MgO interface. The developed technique provides an effective approach to enhancing the interfacial PMA and VCMA properties in the development of voltage-controlled spintronic devices.

  10. Distribution of some heavy and essential metals Cd, Pb, Cu, Fe and Zn in Mango fruit (Mangifera Indica L. cultivated in Different Regions of Pakistan

    Directory of Open Access Journals (Sweden)

    NUSRAT jalbani

    2015-12-01

    Full Text Available  In the present study, the concentrations of Cd, Pb, Cu, Zn and Fe from 50 mango samples (Mangifera indica L. were detected by electro-thermal/flame atomic absorption spectrometry (ETAAS/FAAS. In this study three varieties such as Dusahri, Langra and Chaunsa were collected from different regions (Multan, Sadiqabad, Rahimyar Khan and Mirpurkhas of Pakistan.  The effect of different varieties and environmental conditions on metal accumulation was also investigated. The aim of this study is to compare the level of essential and toxic metal in different regions and correlate the differences observed in metal accumulation to environmental conditions. The accuracy of the conventional acid digestion (CAD method was checked by analyzing Certified Reference Materials (CRM i.e. fortified water (TMDA-70, apple leaves (1515 and standard addition technique. The limit of detections (LODs of the method were found to be 0.113, 2.0, 22.7, 3.85 and 3.05 µg L-1 for Pb, Cd, Cu, Fe, and Zn, respectively.

  11. Hydrogen Production by Ethanol Steam Reforming (ESR over CeO2 Supported Transition Metal (Fe, Co, Ni, Cu Catalysts: Insight into the Structure-Activity Relationship

    Directory of Open Access Journals (Sweden)

    Michalis Konsolakis

    2016-03-01

    Full Text Available The aim of the present work was to investigate steam reforming of ethanol with regard to H2 production over transition metal catalysts supported on CeO2. Various parameters concerning the effect of temperature (400–800 °C, steam-to-carbon (S/C feed ratio (0.5, 1.5, 3, 6, metal entity (Fe, Co, Ni, Cu and metal loading (15–30 wt.% on the catalytic performance, were thoroughly studied. The optimal performance was obtained for the 20 wt.% Co/CeO2 catalyst, achieving a H2 yield of up to 66% at 400 °C. In addition, the Co/CeO2 catalyst demonstrated excellent stability performance in the whole examined temperature range of 400–800 °C. In contrast, a notable stability degradation, especially at low temperatures, was observed for Ni-, Cu-, and Fe-based catalysts, ascribed mainly to carbon deposition. An extensive characterization study, involving N2 adsorption-desorption (BET, X-ray diffraction (XRD, Scanning Electron Microscopy (SEM/EDS, X-ray Photoelectron Spectroscopy (XPS, and Temperature Programmed Reduction (H2-TPR was undertaken to gain insight into the structure-activity correlation. The excellent reforming performance of Co/CeO2 catalysts could be attributed to their intrinsic reactivity towards ethanol reforming in combination to their high surface oxygen concentration, which hinders the deposition of carbonaceous species.

  12. Apply Woods Model in the Predictions of Ambient Air Particles and Metallic Elements (Mn, Fe, Zn, Cr, and Cu at Industrial, Suburban/Coastal, and Residential Sampling Sites

    Directory of Open Access Journals (Sweden)

    Guor-Cheng Fang

    2012-01-01

    Full Text Available The main purpose for this study was to monitor ambient air particles and metallic elements (Mn, Fe, Zn, Cr, and Cu in total suspended particulates (TSPs concentration, dry deposition at three characteristic sampling sites of central Taiwan. Additionally, the calculated/measured dry deposition flux ratios of ambient air particles and metallic elements were calculated with Woods models at these three characteristic sampling sites during years of 2009-2010. As for ambient air particles, the results indicated that the Woods model generated the most accurate dry deposition prediction results when particle size was 18 μm in this study. The results also indicated that the Woods model exhibited better dry deposition prediction performance when the particle size was greater than 10 μm for the ambient air metallic elements in this study. Finally, as for Quan-xing sampling site, the main sources were many industrial factories under process around these regions and were severely polluted areas. In addition, the highest average dry deposition for Mn, Fe, Zn, and Cu species occurred at Bei-shi sampling site, and the main sources were the nearby science park, fossil fuel combustion, and Taichung thermal power plant (TTPP. Additionally, as for He-mei sampling site, the main sources were subjected to traffic mobile emissions.

  13. Fe(III) hydroxide nucleation and growth on quartz in the presence of Cu(II), Pb(II), and Cr(III): metal hydrolysis and adsorption.

    Science.gov (United States)

    Dai, Chong; Hu, Yandi

    2015-01-06

    Fe(III) hydroxide nanoparticles are an essential carrier for aqueous heavy metals. Particularly, iron hydroxide precipitation on mineral surfaces can immobilize aqueous heavy metals. Here, we used grazing-incidence small-angle X-ray scattering (GISAXS) to quantify nucleation and growth of iron hydroxide on quartz in 0.1 mM Fe(NO3)3 solution in the presence of Na(+), Cu(2+), Pb(2+), or Cr(3+) at pH = 3.7 ± 0.1. In 30 min, the average radii of gyration (R(g)) of particles on quartz grew from around 2 to 6 nm in the presence of Na(+) and Cu(2+). Interestingly, the particle sizes remained 3.3 ± 0.3 nm in the presence of Pb(2+), and few particles formed in the presence of Cr(3+). Quartz crystal microbalance dissipation (QCM-D) measurements showed that only Cr(3+) adsorbed onto quartz, while Cu(2+) and Pb(2+) did not. Cr(3+) adsorption changed the surface charge of quartz from negative to positive, thus inhibiting the precipitation of positively charged iron hydroxide on quartz. Masses and compositions of the precipitates were also quantified. This study provided new insights on interactions among quartz, iron hydroxide, and metal ions. Such information is helpful not only for environmental remediation but also for the doping design of iron oxide catalysts.

  14. All-metal uranium bed loading system

    International Nuclear Information System (INIS)

    Eichman, C.C.

    1979-01-01

    The uranium bed processing system is essentially a vacuum system designed to transfer tritium gas from a large shipping container into small, portable containers called beds. The portable beds, designed to contain specific amounts of tritium or deuterium gas, are attached to various production systems for the purpose of hydriding occluder films in the production of neutron generators. The beds are constructed of stainless steel and contain uranium that is hydrided up to 50% capacity with tritium or deuterum gas. This technique not only makes it easy to load a bed, but also to recover surplus gas from a production system after the neutron generator hydriding process has been completed. The process development activities were directed toward solving and developing processing procedures for: (1) purifying the tritium gas; (2) reducing the protium gas; (3) removing helium (due to tritium decay) from the vacuum system; (4) eliminating hydrocarbon contamination; (5) increasing helium pumping speed with ion pumps; (6) providing multiple bed processing capability; (7) measuring pressure accurately; and (8) detect system leaks and obtain residual gas analyses of the system

  15. Microbial mineral transformations at the Fe(II)/Fe(III) redox boundary for solid phase capture of strontium and other metal/radionuclide contaminants. Annual progress report, September 15, 1996--June 15, 1997

    Energy Technology Data Exchange (ETDEWEB)

    Ferris, F.G. [Univ. of Toronto, Ontario (CA). Dept. of Geology; Roden, E.E. [Univ. of Alabama, Tuscaloosa, AL (US). Dept. of Biological Sciences

    1997-01-01

    'The objectives of the project remain the same as those stated in the original proposal. Specifically, to determine microbiological and geochemical controls on carbonate mineral precipitation reactions that are caused by bacterial reduction of Fe(III)-oxides, and identify contributions of these processes to solid phase capture of strontium and other metal/radionuclide contaminants. The project on microbial mineral transformations at the Fe(II)/Fe(III) redox boundary for the solid phase capture of strontium is progressing well. Thus far, the authors have been able to demonstrate that: pH and DIC concentrations increase during microbial reduction of HFO in batch culture experiments with G. metallireducens lasting 30 days with high concentrations of strontium (1.0 \\265m) and calcium (10 \\265m) do not inhibit microbial HFO reduction, the extent of change in pH and DIC concentrations brings about supersaturation with respect to carbonate minerals including siderite (FeCO{sub 3}), strontianite (SrCO{sub 3}), and calcite/aragonite (CaCO{sub 3}); in addition, precipitation of siderite has been documented in cultures of HFO reducing bacteria significant amounts of strontium and calcium (40 to 50% of the total initial concentration) sorb to particulate solids (i.e., HFO and bacteria cells)-in batch culture experiments l sorption of strontium to HFO conforms with Langmuir single site sorption models derived from corresponding mass action and mass balance relationships anticipated from thermodynamic equilibrium considerations the sorption behavior of strontium with S. alga is more complex and seems to involve two sets of reactive surface sites on the bacterial cells; a high affinity site of low total sorption capacity, and a low affinity site with high sorption capacity the total strontium sorption capacities of S. alga and HFO are comparable the observed solid phase partioning of strontium in the culture experiments is in excellent agreement with sorption

  16. Crystallization kinetics and magnetic properties of Fe{sub 66}Nb{sub 4}B{sub 30} bulk metallic glass

    Energy Technology Data Exchange (ETDEWEB)

    Stoica, M., E-mail: m.stoica@ifw-dresden.d [IFW Dresden, Institute for Complex Materials, P.O. Box 270116, D-01171 Dresden (Germany); Kumar, S. [IFW Dresden, Institute for Complex Materials, P.O. Box 270116, D-01171 Dresden (Germany); Roth, S. [IFW Dresden, Institute for Metallic Materials, P.O. Box 270116, D-01171 Dresden (Germany); Ram, S. [Materials Science Centre, Indian Institute of Technology, Kharagpur 721302 (India); Eckert, J. [IFW Dresden, Institute for Complex Materials, P.O. Box 270116, D-01171 Dresden (Germany); Vaughan, G. [European Synchrotron Radiation Facilities ESRF, 38402 Grenoble (France); Yavari, A.R. [LTPCM-CNRS, Institut National Politechnique de Grenoble, 1130 Rue de la Piscine, BP 75, Saint Martin d' Heres Campus 38402 (France)

    2009-08-26

    Fe-based bulk metallic glasses (BMGs) have a high application potential because of their unique soft magnetic properties, mechanical behaviour and high corrosion resistance. Also, they can be obtained directly in the final shape suitable for use as magnetic sensors, magnetic valves, magnetic clutches etc. in different devices. Fe-based alloys able to form magnetic BMGs are of the type transition metal-metalloid and often contain 5 or more elements. Usually, the metalloid content is around 20 at.%. Recently, a new Fe-based BMG containing only 3 elements and a very high boron content was synthesized. The preparation of this BMG was done by employing the copper mold casting method and using the fluxing technique. This new BMG is ferromagnetic, with a Curie temperature around 550 K and a saturation magnetization of 105 Am{sup 2}/kg. Differential scanning calorimetry (DSC) investigations revealed a reduced glass transition temperature of 0.55 and an extension of the supercooled liquid region of about 31 K, values which indicate a relatively good thermal stability. Despite of numerous studies about Fe-based BMGs, there is still a lack of data about the crystallization kinetics. Also, the intermediate metastable phases, which form upon crystallization from the amorphous state, as well as the mechanism of their formation, are not fully understood. The present work discusses the kinetics of the phase formation using the Kissinger analysis and Johnson-Mehl-Avrami plots, correlated with the results obtained upon X-ray diffraction (XRD) of samples with different metastable structures. Additionally, the magnetic behaviour of different phase(s) is presented.

  17. Single-Crystal to Single-Crystal Transformation of a Nonporous Fe(II) Metal-Organic Framework into a Porous Metal-Organic Framework via a Solid-State Reaction.

    Science.gov (United States)

    Spirkl, Sebastian; Grzywa, Maciej; Reschke, Stephan; Fischer, Jonas K H; Sippel, Pit; Demeshko, Serhiy; Krug von Nidda, Hans-Albrecht; Volkmer, Dirk

    2017-10-16

    We report the synthesis of an air-stable nonporous coordination compound based on iron(II) centers, formate anions, and a 4,4'-bipyrazole (H 2 BPZ) ligand. Upon thermal treatment, a porous metal-organic framework (MOF) formed due to decomposition of the incorporated formate anions. This decomposition step and the following structural changes constituted a single-crystal to single-crystal transformation. The resulting [Fe(BPZ)] framework contained tetrahedrally coordinated iron(II) metal centers. The framework was sensitive toward oxidation by molecular oxygen even at temperatures of 183 K, as followed by oxygen sorption measurements and a color change from colorless to metallic black. The semiconductor properties of the oxidized material were studied by diffuse reflectance UV/vis/NIR spectroscopy and dielectric spectroscopy.

  18. Oxygen partial pressure: a key to alloying and discovery in metal oxide--metal eutectic systems

    International Nuclear Information System (INIS)

    Holder, J.D.; Clark, G.W.; Oliver, B.F.

    1978-01-01

    Control of oxygen partial pressure is essential in the directional solidification of oxide--metal eutectic composites by techniques involving gas-solid and gas-liquid interactions. The existence of end components in the eutectic composite is Po 2 sensitive as are melt stoichiometry, solid phase compositions, and vapor losses due to oxidation-volatilization. Simple criteria are postulated which can aid the experimentalist in selecting the proper gas mixture for oxide--metal eutectic composite growth. The Cr 2 O 3 --Mo--Cr systems was used to verify certain aspects of the proposed criteria

  19. The r-process Pattern of a Bright, Highly r-process-enhanced Metal-poor Halo Star at [Fe/H] ∼ ‑2

    Science.gov (United States)

    Sakari, Charli M.; Placco, Vinicius M.; Hansen, Terese; Holmbeck, Erika M.; Beers, Timothy C.; Frebel, Anna; Roederer, Ian U.; Venn, Kim A.; Wallerstein, George; Davis, Christopher Evan; Farrell, Elizabeth M.; Yong, David

    2018-02-01

    A high-resolution spectroscopic analysis is presented for a new highly r-process-enhanced ([Eu/Fe] = 1.27, [Ba/Eu] = ‑0.65), very metal-poor ([Fe/H] = ‑2.09), retrograde halo star, RAVE J153830.9–180424, discovered as part of the R-Process Alliance survey. At V = 10.86, this is the brightest and most metal-rich r-II star known in the Milky Way halo. Its brightness enables high-S/N detections of a wide variety of chemical species that are mostly created by the r-process, including some infrequently detected lines from elements like Ru, Pd, Ag, Tm, Yb, Lu, Hf, and Th, with upper limits on Pb and U. This is the most complete r-process census in a very metal-poor r-II star. J1538–1804 shows no signs of s-process contamination, based on its low [Ba/Eu] and [Pb/Fe]. As with many other r-process-enhanced stars, J1538–1804's r-process pattern matches that of the Sun for elements between the first, second, and third peaks, and does not exhibit an actinide boost. Cosmo-chronometric age-dating reveals the r-process material to be quite old. This robust main r-process pattern is a necessary constraint for r-process formation scenarios (of particular interest in light of the recent neutron star merger, GW170817), and has important consequences for the origins of r-II stars. Additional r-I and r-II stars will be reported by the R-Process Alliance in the near future.

  20. Malonate-bound structure of the glycerophosphodiesterase from Enterobacter aerogenes (GpdQ) and characterization of the native Fe[supscript 2+] metal-ion preference

    Energy Technology Data Exchange (ETDEWEB)

    Jackson, Colin J.; Hadler, Kieran S.; Carr, Paul D.; Oakley, Aaron J.; Yip, Sylvia; Schenk, Gerhard; Ollis, David L. (Queensland); (ANU)

    2010-09-20

    The structure of a malonate-bound form of the glycerophosphodiesterase from Enterobacter aerogenes, GpdQ, has been refined at a resolution of 2.2 {angstrom} to a final R factor of 17.1%. The structure was originally solved to 2.9 {angstrom} resolution using SAD phases from Zn{sup 2+} metal ions introduced into the active site of the apoenzyme [Jackson et al. (2007), J. Mol. Biol. 367, 1047-1062]. However, the 2.9 {angstrom} resolution was insufficient to discern significant details of the architecture of the binuclear metal centre that constitutes the active site. Furthermore, kinetic analysis revealed that the enzyme lost a significant amount of activity in the presence of Zn{sup 2+}, suggesting that it is unlikely to be a catalytically relevant metal ion. In this communication, a higher resolution structure of GpdQ is presented in which malonate is visibly coordinated in the active site and analysis of the native metal-ion preference is presented using atomic absorption spectroscopy and anomalous scattering. Catalytic implications of the structure and its Fe{sup 2+} metal-ion preference are discussed.

  1. Malonate-bound structure of the glycerophosphodiesterase from Enterobacter aerogenes (GpdQ) and characterization of the native Fe[superscript 2+] metal-ion preference

    Energy Technology Data Exchange (ETDEWEB)

    Jackson, Colin J.; Hadler, Kieran S.; Carr, Paul D.; Oakley, Aaron J.; Yip, Sylvia; Schenk, Gerhard; Ollis, David L. (Queensland); (ANU)

    2011-09-28

    The structure of a malonate-bound form of the glycerophosphodiesterase from Enterobacter aerogenes, GpdQ, has been refined at a resolution of 2.2 {angstrom} to a final R factor of 17.1%. The structure was originally solved to 2.9 {angstrom} resolution using SAD phases from Zn{sup 2+} metal ions introduced into the active site of the apoenzyme [Jackson et al. (2007), J. Mol. Biol. 367, 1047-1062]. However, the 2.9 {angstrom} resolution was insufficient to discern significant details of the architecture of the binuclear metal centre that constitutes the active site. Furthermore, kinetic analysis revealed that the enzyme lost a significant amount of activity in the presence of Zn2+, suggesting that it is unlikely to be a catalytically relevant metal ion. In this communication, a higher resolution structure of GpdQ is presented in which malonate is visibly coordinated in the active site and analysis of the native metal-ion preference is presented using atomic absorption spectroscopy and anomalous scattering. Catalytic implications of the structure and its Fe{sup 2+} metal-ion preference are discussed.

  2. Thermoelectric properties of metallic antiperovskites AXD3 (A=Ge, Sn, Pb, Al, Zn, Ga; X=N, C; D=Ca, Fe, Co)

    Science.gov (United States)

    Bilal, Muhammad; Ahmad, Iftikhar; Asadabadi, Saeid Jalali; Ahmad, Rashid; Maqbool, Muhammad

    2015-05-01

    In this paper we communicate the thermoelectric properties of carbon and nitrogen based metallic antiperovskites ANCa3 (A=Ge, Sn, Pb), BCFe3 (B=Al, Zn, Ga) and SnCD3 (D=Co and Fe) using the ab-initio calculations to explore efficient metallic thermoelectric materials. The consistency of the calculated results of SnCCo3 and SnCFe3 with the experimental results confirms the reliability of our theoretical calculations for the other investigated metallic antiperovskites. The results indicate that the thermopower of these materials can be enhanced by changing the chemical potential. The dimensionless figure of merit for the three nitrides approaches 0.96 at room temperature, which proves the usefulness of these materials in thermoelectric generators. Furthermore, the thermal conductivity is minimum at room temperature for chemical potential values between -0.25 μ(eV) and 0.25 μ(eV), and provides the maximum values of dimensionless figure of merit in this range. The striking feature of these studies is identifying a metallic compound, SnNCa3, with the highest value of Seebeck coefficient at room temperature out of all metals. The results anticipate that these materials could be efficient in thermoelectric generators; however, this needs experimental verification.[Figure not available: see fulltext.

  3. 3D Porous Carbon Framework Stabilized Ultra-Uniform Nano γ-Fe2O3: A Useful Catalyst System.

    Science.gov (United States)

    Ai, Yongjian; He, Mengqi; Lv, Qianrui; Liu, Lei; Sun, Hong-Bin; Ding, Mingyu; Liang, Qionglin

    2018-01-04

    We present a novel strategy for the scalable fabrication of γ-Fe 2 O 3 @3DPCF, a three-dimensional porous carbon framework (PCF) anchored ultra-uniform and ultra-stable γ-Fe 2 O 3 nanocatalyst. The γ-Fe 2 O 3 @3DPCF nanocomposites were facilely prepared with the following route: condensation of iron(III) acetylacetonate with acetylacetonate at room temperature to form the polymer precursor (PPr), which was carbonized subsequently at 800 °C. The homogeneous aldol condensation offered an ultra-uniform distribution of iron, so that the γ-Fe 2 O 3 nanoparticles (NPs) were uniformly distributed in the 3D carbon architecture with the average size of approximate 20 nm. The Fe 2 O 3 NPs were capped with carbon, so that the iron oxide maintained its γ-phase instead of the more stable α-phase. The nanocomposite was an excellent catalyst for the reduction of nitroarene; it gave >99 % conversion and 100 % selectivity for the reduction of nitroarenes to the corresponding anilines at 100 °C. The fabrication of the γ-Fe 2 O 3 @3DPCF nanocatalyst represents a green and scalable method for the synthesis of novel carbon-based metal oxide nanostructures. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  4. Strength of "Light" Ferritic and Austenitic Steels Based on the Fe - Mn - Al - C System

    Science.gov (United States)

    Kaputkina, L. M.; Svyazhin, A. G.; Smarygina, I. V.; Kindop, V. E.

    2017-01-01

    The phase composition, the hardness, the mechanical properties at room temperature, and the resistance to hot (950 - 1000°C) and warm (550°C) deformation are studied for cast deformable "light" ferritic and austenitic steels of the Fe - (12 - 25)% Mn - (0 - 15)% Al - (0 - 2)% C system alloyed additionally with about 5% Ni. The high-aluminum high-manganese low-carbon and carbonless ferritic steels at a temperature of about 0.5 T melt have a specific strength close to that of the austenitic steels and may be used as weldable scale-resistant and wear-resistant materials. The high-carbon Fe - (20 - 24)% Mn - (5 - 9)% Al - 5% Ni - 1.5% C austenitic steels may be applied as light high-strength materials operating at cryogenic temperatures after a solution treatment and as scale- and heat-resistant materials in an aged condition.

  5. Studies on the KTa1-xFe xO3-δ system

    International Nuclear Information System (INIS)

    Ciriaco, M. Lurdes F.; Silva Pereira, M.I. da; Nunes, M.R.; Mendonca, M.H.; Costa, F.M.

    2006-01-01

    In this work we have prepared by ceramic route, polycrystalline powders samples derived from the KTaO 3 perovskite by the partial replacement of tantalum by iron with nominal composition KTa 1-x Fe x O 3-δ (0 ≤ x ≤ 1), in order to evaluate the consequence of these substitution on the properties of the compounds. Two synthesis temperatures were used, 973 and 1373 K. From the powders (x = 0.1) iron coatings were prepared and tested, as electrode materials, in alkaline solutions. The characterisation of the powder samples was made by X-ray diffraction (XRD), scanning electron microscopy (SEM) and electrical conductivity measurements. Cyclic voltammetry was used in the electrodes characterisation. The results show that the partial replacement of Ta by Fe and the synthesis temperature affect the properties of the system

  6. Power Management of Hybrid Power Systems with Li-Fe Batteries and Supercapacitors for Mobile Robots

    Directory of Open Access Journals (Sweden)

    Guohui Wang

    2014-05-01

    Full Text Available This paper presents an energy management strategy of a Li-Fe battery and supercapacitor hybrid power system to provide both high power density and energy density for mobile robots with fluctuating workloads. A two-phase power-optimization approach is proposed to exploit the high power density of supercapacitors and the high energy density of Li-Fe batteries. With our strategy, large peak power can be provided for a short time period whenever needed, while low power can be provided for very long time. A set of experiments have been conducted. The experimental results show that our strategy can effectively improve the performance of mobile robots and extend the lifetime of batteries.

  7. Classification of extremely metal-poor stars: absent region in A(C)-[Fe/H] plane and the role of dust cooling

    Science.gov (United States)

    Chiaki, Gen; Tominaga, Nozomu; Nozawa, Takaya

    2017-11-01

    Extremely metal-poor (EMP) stars are the living fossils with records of chemical enrichment history at the early epoch of galaxy formation. By the recent large observation campaigns, statistical samples of EMP stars have been obtained. This motivates us to reconsider their classification and formation conditions. From the observed lower limits of carbon and iron abundances of Acr(C) ∼ 6 and [Fe/H]cr ∼ -5 for C-enhanced EMP (CE-EMP) and C-normal EMP (CN-EMP) stars, we confirm that gas cooling by dust thermal emission is indispensable for the fragmentation of their parent clouds to form such low mass, i.e. long-lived stars, and that the dominant grain species are carbon and silicate, respectively. We constrain the grain radius r_i^cool of a species i and condensation efficiency fij of a key element j as r_C^cool / f_C,C = 10 {μ m} and r_Sil^cool / f_Sil,Mg = 0.1 {μ m} to reproduce Acr(C) and [Fe/H]cr, which give a universal condition 10[C/H] - 2.30 + 10[Fe/H] > 10-5.07 for the formation of every EMP star. Instead of the conventional boundary [C/Fe] = 0.7 between CE-EMP and CN-EMP stars, this condition suggests a physically meaningful boundary [C/Fe]b = 2.30 above and below which carbon and silicate grains are dominant coolants, respectively.

  8. Distinct configurations of antisite defects in ordered metal phosphates: comparison between LiMnPO4 and LiFePO4.

    Science.gov (United States)

    Chung, Sung-Yoon; Choi, Si-Young; Lee, Seongsu; Ikuhara, Yuichi

    2012-05-11

    By using a combination of aberration-corrected high-angle annular dark-field scanning transmission electron microscopy, ab initio density-functional theory calculations, and neutron powder diffraction techniques, We have found completely different configurations of the antisite exchange defects in LiMnPO4 and LiFePO4, with a random distribution of the exchange pairs without aggregation in the former and with zigzag-type clustering behavior preferred in the latter. Recalling the compositional analogy and identical crystal structure of the two metal phosphates, such unexpectedly distinct arrangement of the same type of point defects is a notable structural aspect.

  9. Metallization systems for stable ohmic contacts to GaAs

    International Nuclear Information System (INIS)

    Tandon, J.L.; Douglas, K.D.; Vendura, G.; Kolawa, E.; So, F.C.T.; Nicolet, M.A.

    1986-01-01

    A metallization scheme to form reproducible and stable ohmic contacts to GaAs is described. The approach is based on the configuration: GaAs/X/Y/Z; where X is a thin metal film (e.g. Pt, Ti, Pd, Ru), Y is an electrically conducting diffusion barrier layer (TiN, W or W/sub 0.7/N/sub 0.3/), and Z is a thick metal layer (e.g. Ag) typically required for bonding or soldering purposes. The value and reproducibility of the contact resistance in these metallization systems results from the uniform steady-state solid-phase reaction of the metal X with GaAs. The stability of the contacts is achieved by the diffusion barrier layer Y, which not only confines the reaction of X with GaAs, but also prevents the top metal layer Z from interfering with this reaction. Applications of such contacts in fabricating stable solar cells are also discussed

  10. Biosurfactant assisted synthesis of Fe3O4@rhamnolipid@BiOBr and its behaviour in plasma discharge system

    International Nuclear Information System (INIS)

    Wang, Li; Yu, Zebin; Hou, Yanping; Peng, Zhenbo; Zhang, Li; Meng, Zhengcheng; Li, Fengyuan; He, Jun; Huang, Junlin

    2016-01-01

    A novel Fe 3 O 4 @rhamnolipid@BiOBr (FRB) was synthesized via a modified precipitation method and applied in the plasma discharge system. Rhamnolipid was used as biosurfactant to modify Fe 3 O 4 by interacting with Fe 3 O 4 via its aliphatic chain. The results show that the prepared FRB magnetic photocatalyst exhibited excellent photocatalytic activity and Fenton reaction behavior in the plasma discharge system. Meanwhile, the addition of FRB could improve energy efficiency of defluorination by 21.29 mg kW −1 h −1 . (paper)

  11. Buckminsterfullerenes: a non-metal system for nitrogen fixation.

    Science.gov (United States)

    Nishibayashi, Yoshiaki; Saito, Makoto; Uemura, Sakae; Takekuma, Shin-Ichi; Takekuma, Hideko; Yoshida, Zen-Ichi

    2004-03-18

    In all nitrogen-fixation processes known so far--including the industrial Haber-Bosch process, biological fixation by nitrogenase enzymes and previously described homogeneous synthetic systems--the direct transformation of the stable, inert dinitrogen molecule (N2) into ammonia (NH3) relies on the powerful redox properties of metals. Here we show that nitrogen fixation can also be achieved by using a non-metallic buckminsterfullerene (C60) molecule, in the form of a water-soluble C60:gamma-cyclodextrin (1:2) complex, and light under nitrogen at atmospheric pressure. This metal-free system efficiently fixes nitrogen under mild conditions by making use of the redox properties of the fullerene derivative.

  12. Study of Moessbauer effect on LiFe5-x Alx O8, LiFe 5-x Gax O8 and LiGa5-x Fex O8 systems

    International Nuclear Information System (INIS)

    Barthem, V.M.T.S.

    1982-01-01

    The measures obtained by Moessbauer spectroscopy from LiFe 5-x Ga x O 8 and LiFe 5-x Al x O 8 systems are presented. A comparative study of the influences of dopant diamagnetic ions on magnetic structures of lithium ferrite was performed. The LiGa 5-x Fe x O 8 systems were analysed based on the existing data from LiAl 5-x Fe x O 8 systems, otaining informations about the iron ion behaviour in both matrices. (M.C.K.) [pt

  13. Magneto-elastic properties and electronic structure analysis of the (Fe1-xNix)2P system

    International Nuclear Information System (INIS)

    Zach, R.; Tobola, J.; Sredniawa, B.; Kaprzyk, S.; Casado, C.; Bacmann, M.; Fruchart, D.

    2004-01-01

    For the (Fe 1-x Ni x ) 2 P compounds with x=0.015, 0.02, 0.025 and 0.25, both X-ray diffraction and χ ac susceptibility experiments under pressure up to 1.5 GPa were performed from 80 to 420 K. For all the studied compounds, a clear cut metal atom distribution was found on the basis of the Fe 2 P structure-type (SG: P6-bar2m), the 3g sites being fully occupied by Fe, while both Fe and Ni are randomly distributed on the 3f sites. The variation of the ordering temperature under pressure ∂T C /∂p increases from negative values for all studied compounds up to zero for the Ni-rich one (Fe 0.75 Ni 0.25 ) 2 P. Additionally for the latter, neutron diffraction experiments were carried out in the 10-290 K range to characterise the transformation between the ferromagnetic (F) and paramagnetic (P) states. An electronic structure analysis of the (Fe 1-x Ni x ) 2 P compounds performed using the Korringa-Kohn-Rostoker method with the coherent potential approximation (KKR-CPA) shows that the total energy calculation fully supports the Ni preference for the 3f occupancy. Accounting to this trend, the calculated total magnetic moment was found to decrease almost linearly with x, in very fair agreement with the experimental data when measured for x 0.75 Ni 0.25 ) 2 P remain in satisfying agreement with the results of neutron diffraction. Hence, it is suggested that the strong electron polarisation at E F (P ∼ 90%) as established theoretically for the (Fe 1-x Ni x ) 2 P compounds having the smallest Ni content, can be responsible for the marked magneto-elastic phase transition as observed, e.g. in (Fe 0.975 Ni 0.025 ) 2 P

  14. Constitutive modeling of two-phase metallic composites with application to tungsten-based composite 93W–4.9Ni–2.1Fe

    International Nuclear Information System (INIS)

    Lu, W.R.; Gao, C.Y.; Ke, Y.L.

    2014-01-01

    The two-phase metallic composites, composed by the metallic particulate reinforcing phase and the metallic matrix phase, have attracted a lot of attention in recent years for their excellent material properties. However, the constitutive modeling of two-phase metallic composites is still lacking currently. Most used models for them are basically oriented for single-phase homogeneous metallic materials, and have not considered the microstructural evolution of the components in the composite. This paper develops a new constitutive model for two-phase metallic composites based on the thermally activated dislocation motion mechanism and the volume fraction evolution. By establishing the relation between microscopic volume fraction and macroscopic state variables (strain, strain rate and temperature), the evolution law of volume fraction during the plastic deformation in two-phase composites is proposed for the first time and introduced into the new model. Then the new model is applied to a typical two-phase tungsten-based composite – 93W–4.9Ni–2.1Fe tungsten heavy alloy. It has been found that our model can effectively describe the plastic deformation behaviors of the tungsten-based composite, because of the introduction of volume fraction evolution and the connecting of macroscopic state variables and micromechanical characteristics in the constitutive model. The model's validation by experimental data indicates that our new model can provide a satisfactory prediction of flow stress for two-phase metallic composites, which is better than conventional single-phase homogeneous constitutive models including the Johnson–Cook (JC), Khan–Huang–Liang (KHL), Nemat-Nasser–Li (NNL), Zerilli–Armstrong (ZA) and Voyiadjis–Abed (VA) models

  15. An -OH group functionalized MOF for ratiometric Fe3+ sensing

    Science.gov (United States)

    Xu, Hui; Dong, Yingying; Wu, Yuhang; Ren, Wenjing; Zhao, Tao; Wang, Shunli; Gao, Junkuo

    2018-02-01

    Iron is one of the most important elements in the biochemical processes in all living system, both deficiency or excess of iron will lead to metabolism disorder diseases. However, Fe3+ is one of the most efficient fluorescence quenchers among the transition-metal ions because of its paramagnetic nature. The realization of Fe3+ ratiometric and self-calibrated fluorescent sensor is highly-challenging. We synthesized a novel luminescent -OH functionalized EuOHBDC (Eu2(OH-BDC)3, OH-BDC=2-hydroxyterephthalic acid) by hydrothermal reaction and in situ ligand synthesis, and used it as a rare ratiomatric luminescent sensor for Fe3+ ions. The -OH functional group facilitates both electron transfer and binding interaction between EuOHBDC and Fe3+, which lead to luminescent quenching of ligand-based emission while enhancement of a new peak emission, and thus enables ratiometric detection of Fe3+. The relative fluorescent intensity ratio (I375/I427) increased linearly with increasing Fe3+ concentration in the 10-50 μM range with 1.17 μM (65 ppb) detection limit. The EuOHBDC also shows excellent selectivity towards different metal ions, particularly can discriminate Fe3+ and Fe2+ through different luminescent responses. This result clearly demonstrates the superiority of -OH functionalized MOF for Fe3+ detection, which can contribute to develop high performance luminescent probe for detection of metal ions in environmental and biomedical applications.

  16. Hybrid microcircuit metallization system for the SLL micro actuator

    International Nuclear Information System (INIS)

    Hampy, R.E.; Knauss, G.L.; Komarek, E.E.; Kramer, D.K.; Villaueva, J.

    1976-03-01

    A thin film technique developed for the SLL Micro Actuator in which both gold and aluminum can be incorporated on sapphire or fine grained alumina substrates in a two-level metallization system is described. Tungsten is used as a lateral transition metal permitting electrical contact between the gold and aluminum without the two metals coming in physical contact. Silicon dioxide serves as an insulator between the tungsten and aluminum for crossover purposes, and vias through the silicon dioxide permit interconnections where desired. Tungsten-gold is the first level conductor except at crossovers where tungsten only is used and aluminum is the second level conductor. Sheet resistances of the two levels can be as low as 0.01 ohm/square. Line widths and spaces as small as 0.025 mm can be attained. A second layer of silicon dioxide is deposited over the metallization and opened for all gold and aluminum bonding areas. The metallization system permits effective interconnection of a mixture of devices having both gold and aluminum terminations without creating undesirable gold-aluminum interfaces. Processing temperatures up to 400 0 C can be tolerated for short times without effect on bondability, conductor, and insulator characteristics, thus permitting silicon-gold eutectic die attachment, component soldering, and higher temperatures during gold lead bonding. Tests conducted on special test pattern circuits indicate good stability over the temperature range -55 to +150 0 C. Aging studies indicate no degradation in characteristics in tests of 500 h duration at 150 0 C

  17. Paramagnetic susceptibility of the Zr62Cu22Al10Fe5Dy1 metallic glass subjected to high-pressure torsion deformation

    Science.gov (United States)

    Korolev, A. V.; Kourov, N. I.; Pushin, V. G.; Gunderov, D. V.; Boltynjuk, E. V.; Ubyivovk, E. V.; Valiev, R. Z.

    2017-09-01

    The Zr62Cu22Al10Fe5Dy1 bulk metallic glass is studied in the as-cast state and in the state after processing by high-pressure torsion at temperatures of 20 °C and 150 °C. According to the data from X-ray diffraction and transmission electron microscopy, the structural state of the samples depends weakly on the conducted processing. At the same time, magnetic measurements reveal well recordable changes in paramagnetic susceptibility induced by the processing of the samples. It is assumed that, because of high-pressure torsion deformation, there occurs a noticeable change in the material electronic structure, which leads to a change in the full susceptibility of the samples. The performed studies demonstrate that paramagnetic susceptibility may be an indicator of a change in the structural state of paramagnetic amorphous metallic substances.

  18. Operational management system for warehouse logistics of metal trading companies

    Directory of Open Access Journals (Sweden)

    Khayrullin Rustam Zinnatullovich

    2014-07-01

    Full Text Available Logistics is an effective tool in business management. Metal trading business is a part of metal promotion chain from producer to consumer. It's designed to serve as a link connecting the interests of steel producers and end users. We should account for the specifics warehousing trading. The specificity of warehouse metal trading consists primarily in the fact that the purchase is made in large lots, and the sale - in medium and small parties. Loading and unloading of cars and trucks is produced by overhead cranes. Some part of the purchased goods are shipped in relatively large lots without presales preparation. Another part of the goods undergoes presale preparation. Indoor and outdoor warehouses are used with the address storage system. In the process of prolonged storage the metal rusts. Some part of the goods is subjected to final completion (cutting, welding, coloration in service centers and small factories, usually located at the warehouse. The quantity of simultaneously shipped cars, and the quantity of the loader workers brigade can reach few dozens. So it is necessary to control the loading workers, to coordinate and monitor the performance of loading and unloading operations, to make the daily analysis of their work, to evaluate the warehouse operations as a whole. There is a need to manage and control movement of cars and trucks on the warehouse territory to reduce storage and transport costs and improve customer service. ERP-systems and WMS-systems, which are widely used, do not cover fully the functions and processes of the warehouse trading, and do not effectively manage all logistics processes. In this paper the specialized software is proposed. The software is intended for operational logistics management in warehouse metal products trading. The basic functions and processes of metal warehouse trading are described. The effectiveness indices for logistics processes and key effective indicators of warehouse trading are proposed

  19. Structural and magnetic properties of transition metal substituted BaFe2As2 compounds studied by x-ray and neutron scattering

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Min Gyu [Iowa State Univ., Ames, IA (United States)

    2012-01-01

    The purpose of my dissertation is to understand the structural and magnetic properties of the newly discovered FeAs-based superconductors and the interconnection between superconductivity, antiferromagnetism, and structure. X-ray and neutron scattering techniques are powerful tools to directly observe the structure and magnetism in this system. I used both x-ray and neutron scattering techniques on different transition substituted BaFe2As2 compounds in order to investigate the substitution dependence of structural and magnetic transitions and try to understand the connections between them.

  20. High pressure structural investigation on alluaudites Na{sub 2}Fe{sub 3}(PO{sub 4}){sub 3}-Na{sub 2}FeMn{sub 2}(PO{sub 4}){sub 3} system

    Energy Technology Data Exchange (ETDEWEB)

    Gao, Jing [Key Laboratory of Orogenic Belts and Crustal Evolution, MOE, School of Earth and Space Sciences, Peking University, Beijing 100871 (China); Huang, Weifeng [College of Engineering, Peking University, Beijing 100871 (China); Qin, Shan [Key Laboratory of Orogenic Belts and Crustal Evolution, MOE, School of Earth and Space Sciences, Peking University, Beijing 100871 (China); Wu, Xiang, E-mail: wuxiang@cug.edu.cn [State key laboratory of geological processes and mineral resources, China University of Geosciences, Wuhan 430074 (China)

    2017-03-15

    Alluaudites are promising electrochemical materials benefited from the open structure. Structural variations of alluaudites Na{sub 2}M{sub 3}(PO{sub 4}){sub 3} (M{sub 3}=Fe{sub 3}, Fe{sub 2}Mn and FeMn{sub 2}) system have been studied by synchrotron radiation X-ray diffraction combined with diamond anvil cell technique up to ~10 GPa at room temperature. No phase transition is observed. The excellent structural stability is mainly due to the flexible framework plus strong covalent P-O bond. Mn{sup 2+} instead of Fe can be described as Na{sup +}+2Fe{sup 2+}→Mn{sup 2+}+Fe{sup 3+}+□ where □ represents a lattice vacancy. The replacement of Fe with larger Mn{sup 2+} is equivalent to applying negative chemical pressure to the material. And it causes a more compressible b-axis, lattice expansion, structural compressibility and intensifies the core/electron-electron interactions of Fe. External pressure effect produces anisotropic lattice shrinkage. Structural considerations related to these variations and promising application prospects are discussed. - Graphical abstract: Figure 1 The crystal structure of alluaudites Na{sub 2}M{sub 3}(PO{sub 4}){sub 3} (M{sub 3}=Fe{sub 3}, Fe{sub 2}Mn and FeMn{sub 2}) projected along the c-axis. Alluaudites adopt a flexible framework plus strong covalent P-O bond, which contribute to excellent structural stability up to ~10 GPa. Mn{sup 2+} instead of Fe can be described as Na{sup ++}2Fe{sup 2+}→Mn{sup 2+}+Fe{sup 3+}+□ where □ represents a lattice vacancy, and it is equivalent to applying negative chemical pressure to the host. The substitution causes a more compressible b-axis, lattice expansion, structural compressibility and intensifies the core/electron-electron interactions of Fe.

  1. Electrochemical metal speciation in natural and model polyelectrolyte systems

    NARCIS (Netherlands)

    Hoop, van den M.A.G.T.

    1994-01-01

    The purpose of the research described in this thesis was to examine the applicability of electro-analytical techniques in obtaining information on the speciation of metals, i.e. their distribution over different physico-chemical forms, in aquatic systems containing charged macromolecules.

  2. Quantitative comparison of adhesion in metal-to-plastic systems

    NARCIS (Netherlands)

    Dos Santos Ferreira, O.; Stevens, A.; Schrauwen, C.

    2009-01-01

    A peel test device was used to monitor metal-polymer adhesion. This technique showed variations in the resulting force within 1%, and enabled the ranking of many systems. A change in the 50 nm-adhesion layer resulted in a variation of the fracture energy by a factor 2.3. A change of the substrate

  3. Highly efficient removal of chromium(VI) by Fe/Ni bimetallic nanoparticles in an ultrasound-assisted system.

    Science.gov (United States)

    Zhou, Xiaobin; Jing, Guohua; Lv, Bihong; Zhou, Zuoming; Zhu, Runliang

    2016-10-01

    Highly active Fe/Ni bimetallic nanocomposites were prepared by using the liquid-phase reduction method, and they were proven to be effective for Cr(VI) removal coupled with US irradiation. The US-assisted Fe/Ni bimetallic system could maintain a good performance for Cr(VI) removal at a wide pH range of 3-9. Based on the characterization of the Fe/Ni nanoparticles before and after reaction, the high efficiency of the mixed system could attribute to the synergistic effects of the catalysis of Ni(0) and US cavitation. Ni(0) could facilitate the Cr(VI) reduction through electron transfer and catalytic hydrogenation. Meanwhile, US could fluidize the Fe/Ni nanoparticles to increase the actual reactive surface area and clean off the co-precipitated Fe(III)-Cr(III) hydroxides to maintain the active sites on the surface of the Fe/Ni nanoparticles. Thus, compared with shaking, the US-assisted Fe/Ni system was more efficient on Cr(VI) removal, which achieved 94.7% removal efficiency of Cr(VI) within 10 min. The pseudo-first-order rate constant (kobs) in US-assisted Fe/Ni system (0.5075 min(-1)) was over 5 times higher than that under shaking (0.0972 min(-1)). Moreover, the Fe/Ni nanoparticles still have a good performance under US irradiation after 26 days aging as well as regeneration. Copyright © 2016 Elsevier Ltd. All rights reserved.

  4. Drastic influence of minor Fe or Co additions on the glass forming ability, martensitic transformations and mechanical properties of shape memory Zr–Cu–Al bulk metallic glass composites

    Science.gov (United States)

    González, Sergio; Pérez, Pablo; Rossinyol, Emma; Suriñach, Santiago; Dolors Baró, Maria; Pellicer, Eva; Sort, Jordi

    2014-01-01

    The microstructure and mechanical properties of Zr48Cu48 − xAl4Mx (M ≡ Fe or Co, x = 0, 0.5, 1 at.%) metallic glass (MG) composites are highly dependent on the amount of Fe or Co added as microalloying elements in the parent Zr48Cu48Al4 material. Addition of Fe and Co promotes the transformation from austenite to martensite during the course of nanoindentation or compression experiments, resulting in an enhancement of plasticity. However, the presence of Fe or Co also reduces the glass forming ability, ultimately causing a worsening of the mechanical properties. Owing to the interplay between these two effects, the compressive plasticity for alloys with x = 0.5 (5.5% in Zr48Cu47.5Al4Co0.5 and 6.2% in Zr48Cu47.5Al4Fe0.5) is considerably larger than for Zr48Cu48Al4 or the alloys with x = 1. Slight variations in the Young’s modulus (around 5–10%) and significant changes in the yield stress (up to 25%) are also observed depending on the composition. The different microstructural factors that have an influence on the mechanical behavior of these composites are investigated in detail: (i) co-existence of amorphous and crystalline phases in the as-cast state, (ii) nature of the crystalline phases (austenite versus martensite content), and (iii) propensity for the austenite to undergo a mechanically-driven martensitic transformation during plastic deformation. Evidence for intragranular nanotwins likely generated in the course of the austenite–martensite transformation is provided by transmission electron microscopy. Our results reveal that fine-tuning of the composition of the Zr–Cu–Al–(Fe,Co) system is crucial in order to optimize the mechanical performance of these bulk MG composites, to make them suitable materials for structural applications. PMID:27877691

  5. 3D FE Analysis of RC Beams Externally Strengthened with SRG/SRP Systems

    Directory of Open Access Journals (Sweden)

    Francesco Bencardino

    2016-05-01

    Full Text Available The purpose of this study is to evaluate, through a nonlinear Finite Element (FE analysis, the structural behavior of Reinforced Concrete (RC beams externally strengthened by using Steel Reinforced Grout (SRG and Steel Reinforced Polymer (SRP systems. The parameters taken into account were the external strengthening configuration, with or without U-wrap end anchorages, as well as the strengthening materials. The numerical simulations were carried out by using a three-dimensional (3D FE model. The linear and nonlinear behavior of all materials was modeled by appropriate constitutive laws and the connection between concrete substrate and external reinforcing layer was simulated by means of cohesive surfaces with appropriate bond-slip laws. In order to overcome convergence difficulties, to simulate the quasi-static response of the strengthened RC beams, a dynamic approach was adopted. The numerical results in terms of load-displacement curves, failure modes, and load and strain values at critical stages were validated against some experimental data. As a result, the proposed 3D FE model can be used to predict the structural behavior up to ultimate stage of similar strengthened beams without carrying out experimental tests.

  6. Geochemical modelling and speciation studies of metal pollutants present in selected water systems in South Africa

    Science.gov (United States)

    Magu, M. M.; Govender, P. P.; Ngila, J. C.

    2016-04-01

    Metal pollutants in water poses great threats to living beings and hence requires to be monitored regularly to avoid loss of lives. Various analytical methods are available to monitor these pollutants in water and can be improved with time. Modelling of metal pollutants in any water system helps chemists, engineers and environmentalists to greatly understand the various chemical processes in such systems. Water samples were collected from waste water treatment plant and river from highlands close to its source all the way to the ocean as it passing through areas with high anthropogenic activities. Pre-concentration of pollutants in the samples was done through acid digestion and metal pollutants were analysed using inductively coupled plasma-optical emission spectra (ICP-OES) to determine the concentration levels. Metal concentrations ranged between 0.1356-0.4658 mg/L for Al; 0.0031-0.0050 mg/L for Co, 0.0019-0.0956 mg/L for Cr; 0.0028-0.3484 mg/L for Cu; 0.0489-0.3474 mg/L for Fe; 0.0033-0.0285 mg/L for Mn; 0.0056-0.0222 mg/L for Ni; 0.0265-0.4753 mg/L for Pb and 0.0052-0.5594 mg/L for Zn. Modelling work was performed using PHREEQC couple with Geochemist's workbench (GWB) to determine speciation dynamics and bioavailability of these pollutants. Modelling thus adds value to analytical methods and hence a better complementary tool to laboratory-based experimental studies.

  7. Oxalate enhanced degradation of Orange II in heterogeneous UV-Fenton system catalyzed by Fe3O4@γ-Fe2O3composite.

    Science.gov (United States)

    Dai, Huiwang; Xu, Shuying; Chen, Jianxin; Miao, Xiaozeng; Zhu, Jianxi

    2018-05-01

    Oxalate enhanced mechanism of Fe 3 O 4 @γ-Fe 2 O 3 was developed to prov